| Tag | Content |
|---|
EnhancerAtlas ID | HS012-01588 |
Organism | Homo sapiens |
Tissue/cell | Caco-2 |
Coordinate | chr10:71657290-71658450 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HNF4G | MA0484.1 | chr10:71658410-71658425 | TGGCCTTTGCCCTCT | - | 7.14 | | Zfx | MA0146.2 | chr10:71658177-71658191 | GAGGCCGAGGCCGG | - | 6.28 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_33670 | chr10:71654769-71663943 | H2171 | | SE_37373 | chr10:71653700-71662752 | HSMMtube |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH10I069895 | chr10 | 71654829 | 71657704 | | GH10I069898 | chr10 | 71657821 | 71662304 |
|
Enhancer Sequence | TGTAGGTTCT GGAAGGTCTC CGGGCCCCTC TCCACTGAGA GGCTTCCTGA ACATACAGCC 60
CAACATTGCA CATCCCCAGG CCCCGGCAGT GGGAGCGGGT GGAGCTCTGT GTGCCACTGC 120
TGTCCAAGAA GGCAGCAGCT GTGACCTGGA AAGGCCACAC TTGGGCTCCC CATCCCCAGC 180
TGGGCGCATT CGCAGCCCAA GCAGCTCCTG GTTCTTAACA CTCATCCCAG GAGTCTCGTG 240
TGATTTAAGC GCTTTCAAAA ACAAGCAGCT GATGACAGTA TATGCCATCT TTGTTTTCAC 300
ATGGGCTCTG ATGGCCTCCT AAAGCCACGG GTTGCTCAGC TTCAATGGGT AGAGGGACTG 360
GAAGCTGCAA CAATTTCCAG AAATGAAAAT CACATTAGAT AATATGACTG CAAGTTGCCT 420
CCCGCAAAAA CGTGGTTGAG CTTTCTGGAG ATATCTTTGC CCAGCCTCTA TCTTCCAGGC 480
CCCGCAGCCC CAGGGTGAGC CCTCAGCAGC ACTTAACATG TGCCCACGCT GGCCTCACCC 540
TCAGCCAGCT CAAACCCCGG GGAACTGGGC TTGGCACTGC CCTTGACCAC CCTCCCCAGA 600
TGCGCTGACA CCAGCCTTTC TTGCTCAACC AAAAAAAGAA CCCACCAGCC GCACACCAGC 660
CCAACTTCAA GTACCAATTT CACGGGCCCG GTGGTTCCCT GGCCAGAGCC TCTGAGTTGG 720
CTCCCTTCTG TCCCCCAAGC AGGGATGGGT GGGGCTGGCA GTGCAACGTT GGGCTGTGTG 780
TCCAGCAGCC TCTGCAGCCC AGCATGGCCA CGGAGGGCAA GCCTGGCCAT GTGGGAGCCA 840
CTGTCCCATT CCGGGGGCTG CTGGTCAACA TCCCAAACTC TGACCTGGAG GCCGAGGCCG 900
GGTGTGGACT GAGGGCCACA ACTCCTCCTA AGGGACGGCT GTGCCATCCA AGGGCAAGCT 960
CCGCTCTGCA TCCTCAAGCC GTGAGAGTGC CCTGTCCACT CCTTCCCTCC CACTCCTCAT 1020
GTGCACGCTA ATCTCTCTTC TCTCTTCCTC TGCTCCGGTC CCTCTTGGTT GCCCTGCCCT 1080
CCTGGTGACT TTTGGCATCG ATCTGAATAC CTGTGATCTT TGGCCTTTGC CCTCTGGCCC 1140
TCCAACTCAT CTTTCTCCTC 1160
|
