| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:119892544-119892785 | Common:3; Rare:92 | ||||
| chr10:120851158-120851447 | Common:5; Rare:104 | ||||
| chr10:121927874-121928068 | Common:1; Rare:76 | ||||
| chr10:121928429-121928536 | Rare:28 | ||||
| chr10:122879531-122879706 | Common:3; Rare:46 | ||||
| chr10:122954181-122954516 | Common:1; Rare:121 | ||||
| chr10:122980371-122980492 | Common:1; Rare:40 | ||||
| chr10:123008791-123009028 | Common:5; Rare:66; Clinvar:4; Clinvar (benign):5 | ||||
| chr10:124092365-124092597 | Common:1; Rare:57 | ||||
| chr10:124093498-124093665 | Common:2; Rare:32 | ||||
| chr10:124418881-124419092 | Common:4; Rare:98; Clinvar:3; Clinvar (benign):1 | ||||
| chr10:124461727-124461882 | Common:4; Rare:58 | ||||
| chr10:124791750-124791984 | Common:1; Rare:123 | ||||
| chr10:125719453-125719802 | Common:1; Rare:132 | ||||
| chr10:125823159-125823621 | Common:2; Rare:169; Clinvar:1; Clinvar (benign):2 |