| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:4831684-4831763 | Rare:23 | ||||
| chr19:4867626-4867859 | Common:3; Rare:69 | ||||
| chr19:5293197-5293418 | Common:1; Rare:100 | ||||
| chr19:5340679-5341033 | Common:1; Rare:134 | ||||
| chr19:5622729-5623217 | Common:5; Rare:196 | ||||
| chr19:5680474-5680680 | Rare:70 | ||||
| chr19:5680685-5681199 | Rare:140 | ||||
| chr19:5978062-5978383 | Common:3; Rare:120 | ||||
| chr19:6217020-6217318 | Common:1; Rare:58 | ||||
| chr19:6361490-6361801 | Common:1; Rare:122; Clinvar:2; Clinvar (benign):5 | ||||
| chr19:6372553-6372827 | Common:3; Rare:92 | ||||
| chr19:6393097-6393222 | Common:2; Rare:30 | ||||
| chr19:6393412-6393580 | Common:2; Rare:50 | ||||
| chr19:6502187-6502438 | Rare:72; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
| chr19:7395014-7395185 | Common:6; Rare:51 |