| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:244049003-244049205 | Common:1; Rare:55 | ||||
| chr1:244451782-244452365 | Common:5; Rare:470 | ||||
| chr1:244454280-244454780 | Common:3; Rare:86 | ||||
| chr1:244461130-244461641 | Common:7; Rare:406 | ||||
| chr1:244461693-244461917 | Rare:83 | ||||
| chr1:244652670-244653246 | Common:11; Rare:418 | ||||
| chr1:244653232-244653632 | Common:4; Rare:165 | ||||
| chr1:244834594-244835490 | Common:5; Rare:641 | ||||
| chr1:244835480-244835775 | Common:10; Rare:302; Clinvar:2; Clinvar (benign):15 | ||||
| chr1:244862880-244863370 | Common:13; Rare:456 | ||||
| chr1:244863404-244863545 | Common:5; Rare:60 | ||||
| chr1:244863828-244864190 | Common:2; Rare:189; Clinvar:9; Clinvar (benign):12 | ||||
| chr1:244864248-244864811 | Common:2; Rare:457 | ||||
| chr1:244969762-244970451 | Common:14; Rare:633 | ||||
| chr1:244970480-244970954 | Common:22; Rare:380 |