| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:112645701-112645944 | Common:1; Rare:89 | ||||
| chr2:113627069-113627250 | Common:1; Rare:51 | ||||
| chr2:113756556-113756769 | Common:3; Rare:72 | ||||
| chr2:113889710-113890171 | Common:8; Rare:151 | ||||
| chr2:118014033-118014237 | Common:2; Rare:111 | ||||
| chr2:118088145-118088526 | Common:2; Rare:102 | ||||
| chr2:119366779-119367054 | Common:1; Rare:83 | ||||
| chr2:121530607-121530884 | Common:7; Rare:115 | ||||
| chr2:121736828-121737111 | Common:4; Rare:107 | ||||
| chr2:127294086-127294219 | Common:2; Rare:53; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:127526445-127526598 | Common:1; Rare:46 | ||||
| chr2:128091031-128091349 | Common:8; Rare:105 | ||||
| chr2:130181555-130181784 | Common:3; Rare:99 | ||||
| chr2:130342127-130342211 | Rare:37 | ||||
| chr2:130342802-130342946 | Common:2; Rare:60 |