| Tag | Content |
|---|
EnhancerAtlas ID | HS012-26257 |
Organism | Homo sapiens |
Tissue/cell | Caco-2 |
Coordinate | chr9:126985000-126986210 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HNF4G | MA0484.1 | chr9:126985755-126985770 | AGAGTCCAAAGTTCA | + | 8.33 | | Stat6 | MA0520.1 | chr9:126985888-126985903 | GTTTCTCTGGAAGAG | - | 6.54 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_09686 | chr9:126975691-126986742 | CD14 | | SE_59974 | chr9:126945864-126986288 | Ly4 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr9 | 126985067 | 126986200 | | chr9 | 126985233 | 126986085 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH09I124220 | chr9 | 126982280 | 126986678 |
|
Enhancer Sequence | GGACATCCAT GTTACCTGCA CTCATGTGTA GTAAAGAGGT CATGCGTGTT TACAAACCAT 60
AGTACCACCA CAGAGACCAC AGGCCCAGCA AATGGGGCTC ACACAGGCAT GCACACACAC 120
ACACGTATCC TTGATGGTAA ACATGCCCAC CCACCATTGT GCACACATGC GTGTATTTAC 180
ACCCACATGC ACACTCATCG GCACACAATC AGAGCCACAC ACCTGCACGT GCCCCCACAG 240
AATCACACGT GTGTGCAGTC TCACCTATCT GCACTCTGCC ATGGGCCCCA TTACATACAT 300
GCATGCAAAC AGATAACACA CACGCCTATC AATAGCCAGG ATGACTCACA CACGAGGACA 360
CACATCATAC CCTCACAGAC TCGTGCATGG ACCACCCTGC AGTCACAAAG CAGCATCCAG 420
CATCCGACAA TCTGCTGATG TCACTCCCCT GAGAGTAACC ATGGCTCCAT GCATAGGCAG 480
AGGCAACTCA GCTCACAGGT GCCGCCTGTC CACATGCAGA CACAGACACA CACACACATA 540
CACACACACA CACTCTGACA GTTCCCCAAT GGCCAGCCTC CTCCACTGAC TCCCCACAGC 600
CAGGTGCTCT GACACCCTCC TTGGTGGGAC CCTCTCTCTT CAAGGCGCCC AGAGCCACCT 660
GGCTGTCCTT GGAACTAAGT GAGCACCCTG CCCACCCCCA GCCTTGTCCC CTAAACTGGG 720
TGGTTTAGGT CTGAGGGGTG GGGAGAAGGC TGCCCAGAGT CCAAAGTTCA GGGGCCAACA 780
TCTTGTTTGC AGGCGCTGGT GGAAATTGCA CAACCTGCCA GCTGGGTGAC TTGGGCTTAT 840
TGTCTCTGAG TTCCCCTTGG CTGCAGGCCC AAGCCCAGCC AGTGACCTGT TTCTCTGGAA 900
GAGGGTGGGG AAAGTGGTTC CTCCCTCCCC TGCCTGGGGA ACTGGTGGCC CTCCCTGGGC 960
ACTGGTGGCT GGTCCCCAGC TATGTGTGCA ACACACCTGA CACTGAGATG CACAGAACTC 1020
AGCATCCAAC CTGTCCTTTC CCAGATAGGA AACTGAAGCT CAGGGAAGGA AAGGCTTGCC 1080
CAGGGTCACC CAGCAAGGAG GCCCAGGAGG ACTGGAACTC AGGCTCAGTT TCCTTTCTTT 1140
TCTTTTCTTT TTTTTTGTGA TGGAGTCTCA CTCTGTGGCC CAGGCTCGAG TGCAGTGGCG 1200
TGATCTTAGC 1210
|
