| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:103562619-103563075 | Common:8; Rare:180; Clinvar (benign):5 | ||||
| chr14:103629081-103629409 | Common:2; Rare:130 | ||||
| chr14:103715470-103715853 | Common:1; Rare:123 | ||||
| chr14:104724073-104724237 | Common:1; Rare:65 | ||||
| chr14:104752826-104753270 | Common:3; Rare:153 | ||||
| chr15:23039539-23039714 | Common:1; Rare:70 | ||||
| chr15:25438969-25439229 | Common:3; Rare:98 | ||||
| chr15:28738371-28738497 | Common:1; Rare:23 | ||||
| chr15:30903645-30903943 | Common:2; Rare:79 | ||||
| chr15:30991516-30991971 | Common:6; Rare:164 | ||||
| chr15:31365918-31366155 | Common:2; Rare:59 | ||||
| chr15:32615127-32615630 | Common:7; Rare:124 | ||||
| chr15:34101828-34102117 | Common:1; Rare:62 | ||||
| chr15:34318754-34318909 | Common:2; Rare:36 | ||||
| chr15:34582807-34582930 | Rare:39 |