| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:117366930-117367200 | Rare:78 | ||||
| chr1:117367220-117367650 | Common:30; Rare:534 | ||||
| chr1:117367896-117368076 | Common:1; Rare:54 | ||||
| chr1:117368342-117368934 | Common:2; Rare:211 | ||||
| chr1:117605696-117606125 | Common:8; Rare:632 | ||||
| chr1:117929500-117930030 | Common:27; Rare:690 | ||||
| chr1:118184709-118185448 | Common:7; Rare:540 | ||||
| chr1:118185590-118185940 | Rare:60 | ||||
| chr1:118987067-118987802 | Common:3; Rare:218 | ||||
| chr1:118987754-118988760 | Common:1; Rare:527 | ||||
| chr1:119140070-119140541 | Common:6; Rare:273 | ||||
| chr1:119140607-119140905 | Common:7; Rare:433 | ||||
| chr1:119140829-119141537 | Common:2; Rare:196 | ||||
| chr1:119648098-119648608 | Common:19; Rare:527 | ||||
| chr1:119711597-119712006 | Common:2; Rare:98; Clinvar:4; Clinvar (benign):2 |