| Tag | Content |
|---|
EnhancerAtlas ID | HS118-10663 |
Organism | Homo sapiens |
Tissue/cell | Liver |
Coordinate | chr2:178146100-178148230 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Foxd3 | MA0041.1 | chr2:178147938-178147950 | GAATGTTTGTTT | + | 7.22 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_26714 | chr2:178146124-178148074 | Esophagus |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH02I177281 | chr2 | 178145928 | 178147728 | | GH02I177283 | chr2 | 178148190 | 178149548 |
|
Enhancer Sequence | AAAAGTTTAA AATTAGGTGC CTGACATTTA AGGGAAAAAG TCCAAAGTTA ATCAAGGATG 60
ACCGCTTATT GCAAGATTCA AAACCTCTAA ATGACAAAAC TTCTAAAAAA GGAAATGATG 120
ATAGCACGGG GAACCCTGCT GATCCATCTC CCTGCCCAAA TACTTCTCCA TTCCCAACAT 180
CTGTGCAGCC ATGTGCAGCA GAGACAAACA GCAGCAGCAC TCCACCCCCA AGCTTTGAGA 240
ACCGCAGAGC TGTGGCTGAC ACAGTGGTCC TATCTCTGTG AAGTACACAA ACCATACCAC 300
AGCCTTATTT TCTGAGACCA TCTCTATGTA ACCAGCTTCC CTAAATGCTG TGGCCCAAGA 360
GGCTAACACT TTGGTCAGTC ATGGGGCAAT ATGGCTGCTC CCACATGGCA TCCAAGTCCA 420
TGCTTAGAGA CTGAAGGGGA GCCAGCCTTG GTAAACCAGG TCTGTGGTCA TTTCCCCACC 480
TGGCATTTTT GAGCTGTACC AAGCAGCCTA GGGGTTCTTA CTGCAAGGGC ACGCTCAAAC 540
CTGACTTGTC CAGACAAGCA GAAGAGTTTT GGGCTCCCAA TCGAGCACGG TGGTCAGTCT 600
GTTCCAGTTT GTCTGGGACT TTCCAGGTTT GAACACTGAA AGTTCTACAG CCAGGAAATC 660
CCTCAGTCCC AGGCAAACTG GGATGGTTGG TCACCCTGAA GTCAAGACAC CTAGGCTTTG 720
GCACCTAAAC ATCAGTTTCC TCATCTGTAA AATGCTGGGA CTGGCCAGTA CAGCTTCTGA 780
TGTTACTGCC ACATCTAATA GTCCATGATT CACTCTCATG CTCCTGACCT TACCCATCTG 840
CAGCCCAACT CCCAAACAAA CTTCACTTGA TCCAAGATCG AGTTCATGTA ACCTGATAAG 900
CTAATCATTA GTGTGTTAAC AGGAGAGGAT TATAGGGTTC ACAGTTGAAT TTTAACAATG 960
GCTCGGGTGG AAGGCATGTG GGTAGCTGAG TCGTTCTAAT GGTGGGAAGT TCAGCTGGGG 1020
AGATGGAGTG TATGGCTCTG TGCCATCTGA GAGAAAGATA TTTTTAGGCA GGCAGGTTTT 1080
GAGGCAGCCA GCCTGAGAGA GCTGGTTTGA TGGGCTGCTT TTAGCTGCAC AGCAGGAACA 1140
GGCCACAGGC AGGGCAGTCT TGTCTGACTT GAGCCAACTT TCACACTATG ACCTGAATAA 1200
AATCAGCAGT TGAAGCCACA GACTGGAGAA GAAAGGATGT AGTCTGCTGA TAGCAATATA 1260
TATGTATATA ATGCATTTGC TTTGAGCCTG GGTCTGTCAT CTATAATACA GATATGTAGC 1320
TATGATCCTG GGTAGTTGAG AGTTCAGACT CTGGGATCAC CACCTACCAA CTCTGTGATA 1380
TTGGGCAAGT TGTAGACTGA ATAATATGCA TTTGCTGATA TTTAACCTTT TTGATCTACA 1440
CACACAGGAA TTCCACGTGG TTTAGCCTAA TAGCTTACTC TCTTTTTCCT TGGTTTCCTC 1500
ATGTGTGAAA CGCAGATAGC CACCAAACTT TTCAGGACAC TGTGAGGACC AAATGAGAGG 1560
GACACATAAG GTGGTCAGAA CAGTCCTAGC CCCACAGTCC ATGTCAGTGA TGTCAGCCAC 1620
CACCATCCTA CTGGTGAAGA GGCAGGCATA CAGGGCCATT AGACTCCATC AGCTGAACCT 1680
AGGGTAGCCC AGACTCTTCC TGTCTTCCTG AGACATGGAA CATGGATGAA CCAAAGTGAA 1740
TTGGTCACCT TAGCTGAACT GTAGAACTTC ATTCTAATCC CAGGGTGAGG AAAGGGGAGT 1800
AGGTTCATAC CACAGGTTTT TCAGGTCATT CCAAGACTGA ATGTTTGTTT TTCCTCCCAA 1860
TACAATCAGG TCCTAAGTAT AAAAAAGAGC TTTTTATCAT GAGGTTTTGC TCTAACACCA 1920
TGGAGCCCTT TCTTTAGCCT TACATCTGTC TGTAGCGCCC ACACATGGCC GTCTTCTTCA 1980
ACTTAACTAT ATACACACAC ATACGCATAC ATTGTGAAGC ACATAAGGAA CACATGAGAC 2040
AGCCTCATCA TTATCAGATT ACAAAAAAGT TACACTGAAT TTCTTCTCTC AATAATTAAC 2100
AGGGAGCAAT TCAAAAAGAG GAAACAAAAC 2130
|
