| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:105146235-105146635 | Common:2; Rare:138 | ||||
| chr4:105146759-105146965 | Common:1; Rare:54 | ||||
| chr4:105147408-105147545 | Common:1; Rare:26 | ||||
| chr4:105147659-105148087 | Common:5; Rare:108 | ||||
| chr4:105473364-105473588 | Rare:90 | ||||
| chr4:105474048-105474181 | Common:1; Rare:56 | ||||
| chr4:105708468-105708873 | Common:3; Rare:116 | ||||
| chr4:106316190-106316694 | Common:5; Rare:154 | ||||
| chr4:107719344-107720028 | Common:7; Rare:177 | ||||
| chr4:107720177-107720572 | Common:7; Rare:163 | ||||
| chr4:107824439-107825115 | Common:3; Rare:295 | ||||
| chr4:107931366-107931605 | Common:4; Rare:79 | ||||
| chr4:107989635-107989893 | Common:5; Rare:116; Clinvar:3; Clinvar (benign):4 | ||||
| chr4:108166497-108167025 | Common:4; Rare:134 | ||||
| chr4:108168658-108168763 | Common:1; Rare:21 |