| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:119498700-119499100 | Rare:237 | ||||
| chr3:119676880-119677280 | Common:33; Rare:223 | ||||
| chr3:119677374-119677536 | Rare:53 | ||||
| chr3:120093600-120094086 | Common:5; Rare:262 | ||||
| chr3:120094276-120094810 | Common:9; Rare:286 | ||||
| chr3:120094898-120095317 | Common:2; Rare:113 | ||||
| chr3:120348510-120349046 | Common:4; Rare:188 | ||||
| chr3:120349262-120349456 | Common:4; Rare:132 | ||||
| chr3:120596045-120596511 | Common:4; Rare:248 | ||||
| chr3:120742487-120742825 | Common:4; Rare:174 | ||||
| chr3:121545907-121546119 | Common:3; Rare:98 | ||||
| chr3:121748820-121749300 | Rare:114 | ||||
| chr3:121749631-121750074 | Common:3; Rare:193 | ||||
| chr3:121834957-121835274 | Common:6; Rare:192; Clinvar:12; Clinvar (benign):4 | ||||
| chr3:122383164-122383332 | Common:2; Rare:101 |