| Tag | Content |
|---|
EnhancerAtlas ID | HS091-07187 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr11:17553090-17554800 |
Target genes | |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HNF4G | MA0484.1 | chr11:17553613-17553628 | AGAGGACAAAGTCCA | + | 7.11 | | Hnf4a | MA0114.3 | chr11:17553614-17553630 | GAGGACAAAGTCCACT | + | 6.8 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_28323 | chr11:17551402-17556297 | Fetal_Intestine | | SE_29229 | chr11:17551426-17556292 | Fetal_Intestine_Large |
|
| | 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 |
| GH11I017529 | chr11 | 17551501 | 17556212 |
|
Enhancer Sequence | TGTGGAGATG CCGGGAATGC CTGGAGCCTC ACCCCTGGCC ATGACCTCAG GCACCCAGGG 60
ATTCCAAGAG GAAGCCATTT CAGCCACTGG GCCCAGGCTT AGGAATGGAG TAGACCACTC 120
CTGAAAAGCC CAGAGCTCTT CACACCGGGC CAGTGCCTGA GAAGACTTTG TTCTCTTATA 180
TAAATATCCC CAGGAAACCA GTCTACTAGG GATTGTTGAC TCATTTTGCA GATGAGATGA 240
AGCCAGGATT TCAAACTCAG CGCTGCCTAT CTCGGCTGTT GGGATCTTTC CAGAGGGGAA 300
AGCTCTGTGT GAGATGCTGA CAATTCCTCA CACACTCATC ATCTCCACTC GTATCTGCTG 360
CTAAGCTCTG TCAATTTCAC CTCACCACAG TTCACATGCC TCCTCCCTCA TGCTGTTCAG 420
ACCTTCGACT GCAGCTGCCT GCCCATGTAC TCACTGTCAC GTCATCTTTT CTCAGTGTAA 480
GGCACTCCCT GGCTTAAAAC CCTTTGATGG CCCCTTACTG CCCAGAGGAC AAAGTCCACT 540
CTTCTCAGCA GGCTCAAGGC CCTCCATGAC CTGTCCCCAT GGAGCTTCTC CAGCCTTGTG 600
GCTATTTATG ATCTCCGTGC CCTCCCAAGT CCTACTCCCC CAGATTACTT ATCTCCATTC 660
ACACCCTTGC TTTCATGCCT CCACACTTTG GCTGATGCTG ATCCCTCATT CTGGAATGCC 720
CTTCCCAGAT ATTCCACCTA CCAAAATCTT TTTCTTTTAT TATTATTTTT TTGAGACAGG 780
GTCTTGCTGT CTTGCCCAGG CTGGAGTGCA TTGATGCAAT CATGGCTCAC TGCAGCCTTG 840
ACCTCCTGGG TTCAGGTGAT ATTCCCACCT CAGTCTCCTA AGTAGCTGGG ACTACAGGCA 900
CGCGCCACCA TACCCGGCTA ATTTTTTGTA TTTTTTTGTA GAGATGGGAT TTCACCATGT 960
TGCCCAGGCT GGTCTCTAAC TCTTAGGCTC AAGCAATCCT CCTGCCTCAG CTTCTCAAAG 1020
TTCTGGGATT ACAGGCATGA GCCACCTTGC CTGGCCCCAA ATCTTTCTTA TCCTTCAAAG 1080
CCTTGCTCAA GCCTTCCTGG TCCTTCCTCT TCCCTCGCAG TTGGAAAGGA AAACTCCTTT 1140
CTTCACATTT CTGCTTTTAC CTCTACTTAG CAGTTATTTG ATGTAACTTA TATTAGAGTT 1200
CTTTGTGTTT GCAGTGTATG TTCATCTCCC CTCACCAGAC CACAAGTTAC TCAAGGAAAG 1260
AAATTGGATC TAATTCATTT CCAGATTCTG CACAGTGCCC AGCAGTGGCA GGAGCTTATA 1320
AAGTAGAAAA AATGAATCAA AAAGCAAGTG GGTGATCGGA GACATCTGAT GCAAGGGCTG 1380
TGGCCAGCTG GCATTTCTTG TTCTGTCCCA ACAATCATGC TCTATAGAAT CTATCTGGCT 1440
ACTAGACAGC CTCCTCCATC AGACTGTGAG CAACCTGAAA ACAGAGACCA ATCTGTCTGG 1500
CTCACAACTA TACCCAGCCC CTAGTACAAA GCCAAGTACA AAGTACTTGT GTAAATAGTT 1560
GCTGAAATGA GTGAATGGTA TGTCCATTTG ATTTCCAGGA GCCGTGAGCA TCCACCCTCT 1620
GAGCTCCTCT GTCTCAGAAC AACCCATCCC AGGGCTCCCT GAAGACAAAG GAACCCAAGT 1680
GGCCCACAAG AGCTGGACCC AGCACACTTA 1710
|
