| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:88337598-88338141 | Common:6; Rare:210; Clinvar:7; Clinvar (benign):3 | ||||
| chr11:90134353-90134751 | Common:2; Rare:96 | ||||
| chr11:90222647-90222736 | Common:1; Rare:45 | ||||
| chr11:90222895-90223289 | Common:3; Rare:153 | ||||
| chr11:93197384-93197674 | Common:1; Rare:58 | ||||
| chr11:93197800-93198156 | Common:3; Rare:109 | ||||
| chr11:93330524-93330758 | Common:2; Rare:70 | ||||
| chr11:93542888-93543100 | Common:2; Rare:61 | ||||
| chr11:93543231-93543705 | Common:5; Rare:119 | ||||
| chr11:93543760-93543820 | Rare:14 | ||||
| chr11:93661405-93661884 | Common:1; Rare:124 | ||||
| chr11:93661935-93662112 | Rare:43 | ||||
| chr11:93740864-93741008 | Rare:36 | ||||
| chr11:93741131-93741765 | Common:8; Rare:221 | ||||
| chr11:93741769-93741911 | Rare:23 |