| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:195209810-195210530 | Common:8; Rare:187 | ||||
| chr3:195259924-195260379 | Common:8; Rare:252 | ||||
| chr3:195271058-195271311 | Common:3; Rare:184 | ||||
| chr3:195442930-195443385 | Common:9; Rare:270 | ||||
| chr3:195543234-195543477 | Common:6; Rare:186 | ||||
| chr3:195909510-195910100 | Common:6; Rare:171 | ||||
| chr3:196082046-196082245 | Common:1; Rare:84 | ||||
| chr3:196227610-196227961 | Common:4; Rare:119 | ||||
| chr3:196287546-196287892 | Common:2; Rare:171 | ||||
| chr3:196288210-196288500 | Common:5; Rare:74 | ||||
| chr3:196317650-196318205 | Common:6; Rare:266; Clinvar (pathogenic):2 | ||||
| chr3:196318208-196318350 | Common:2; Rare:105 | ||||
| chr3:196338367-196338629 | Rare:108 | ||||
| chr3:196432382-196432550 | Common:1; Rare:75 | ||||
| chr3:196503566-196503956 | Common:13; Rare:247 |