| Tag | Content |
|---|
EnhancerAtlas ID | HS012-26189 |
Organism | Homo sapiens |
Tissue/cell | Caco-2 |
Coordinate | chr9:114831640-114832350 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF16 | MA0741.1 | chr9:114831970-114831981 | GCCCCGCCCCC | + | 6.02 | | KLF5 | MA0599.1 | chr9:114831970-114831980 | GCCCCGCCCC | + | 6.02 | | RREB1 | MA0073.1 | chr9:114831956-114831976 | CCCCACCCCACCCCGCCCCG | + | 6.47 |
|
| | Number of super-enhancer constituents: 6 | ID | Coordinate | Tissue/cell |
| SE_28204 | chr9:114830690-114833323 | Fetal_Intestine | | SE_29159 | chr9:114826291-114833549 | Fetal_Intestine_Large | | SE_40486 | chr9:114831092-114832404 | K562 | | SE_58816 | chr9:114652459-114841988 | Ly3 | | SE_60959 | chr9:114735912-114841786 | HBL1 | | SE_62263 | chr9:114654503-114840084 | Tonsil |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH09I112068 | chr9 | 114830802 | 114833680 |
|
Enhancer Sequence | TCATTTGTTG AAATGAAGGT CTATGCTATT TTCAAGAGCA GTCCAGAGAG AGATTCTGTA 60
GGATACAGCT GAGAAGACAA CAGCTGGATT CCTGTGGCAG TGATGGAGGA GAGAGGAAAA 120
GCCCACACAT GTCCCCTGGG AACGTACCCC TTCCCCTTTG AGATCGAACT GCCCTCAGGC 180
CCTTTGCTAT CACCGAAATG CCCTTTCACT TGTGACGTTT TGTTGTCACA GTAAAATTAA 240
CTTTTTTTAT TACGTGTCTC CTCTTCTCAG CCAAGGTGGA GATTAACTGG TCACTCTTTT 300
CTGTGTGAGA ACTCCGCCCC ACCCCACCCC GCCCCGCCCC CACCAGCTCT TTACTCCAAG 360
AGTAATAATT CTAGTTCCTC TAATCTCTTG GCTAACATTT TAAAACCACA CAGGAGAAGC 420
AGAACAAAGT ACTCACTGAG CTCAGAAGAG GCAACTGCAG ACCGAGCAGG AAGGCCATCC 480
CCCTGCTTGG TCCAGGTGAT GTCACTCTTT CCCAATCTAG AGTCACAGTT TTCAAGGCAC 540
CACAGTCATC TGGTTCAATC AACATGTGAC TTTGAGACCA TTTTCTGCTC TGTTTGCCTA 600
AGGTCTCCCT GCCCTATATT TTATTTTATT TGTTTTTGTT TTTGTTTTTG CTTTTGCTTT 660
TTGAGATGGA GTTTCGCTCT TGTCGCCCAG GCTGGAGTGC AATGGTGTGA 710
|
