| Tag | Content |
|---|
EnhancerAtlas ID | HS064-08752 |
Organism | Homo sapiens |
Tissue/cell | GM18507 |
Coordinate | chr2:178145900-178148230 |
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 |
|
| | 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 |
| GH02I177281 | chr2 | 178145928 | 178147728 | | GH02I177283 | chr2 | 178148190 | 178149548 |
|
Enhancer Sequence | AAGTGCTGGG ATTACAGGCG TGAGCCACCA TGCCCGGCAT CCTTCCCTTC TTTAGTTTAC 60
ACACATAGGC CCCAGGTACA GGGCATGAGC TAGAGCTGGA TCCCAGCTGA ATGGAAAGCA 120
GGAGGCGCTA TATTGGAAAC AACTGCCAAG CAACCAAGGA CTGGGGACAA AATAGCCTGG 180
GAGGAGAAGT AAAACCAGGA AAAAGTTTAA AATTAGGTGC CTGACATTTA AGGGAAAAAG 240
TCCAAAGTTA ATCAAGGATG ACCGCTTATT GCAAGATTCA AAACCTCTAA ATGACAAAAC 300
TTCTAAAAAA GGAAATGATG ATAGCACGGG GAACCCTGCT GATCCATCTC CCTGCCCAAA 360
TACTTCTCCA TTCCCAACAT CTGTGCAGCC ATGTGCAGCA GAGACAAACA GCAGCAGCAC 420
TCCACCCCCA AGCTTTGAGA ACCGCAGAGC TGTGGCTGAC ACAGTGGTCC TATCTCTGTG 480
AAGTACACAA ACCATACCAC AGCCTTATTT TCTGAGACCA TCTCTATGTA ACCAGCTTCC 540
CTAAATGCTG TGGCCCAAGA GGCTAACACT TTGGTCAGTC ATGGGGCAAT ATGGCTGCTC 600
CCACATGGCA TCCAAGTCCA TGCTTAGAGA CTGAAGGGGA GCCAGCCTTG GTAAACCAGG 660
TCTGTGGTCA TTTCCCCACC TGGCATTTTT GAGCTGTACC AAGCAGCCTA GGGGTTCTTA 720
CTGCAAGGGC ACGCTCAAAC CTGACTTGTC CAGACAAGCA GAAGAGTTTT GGGCTCCCAA 780
TCGAGCACGG TGGTCAGTCT GTTCCAGTTT GTCTGGGACT TTCCAGGTTT GAACACTGAA 840
AGTTCTACAG CCAGGAAATC CCTCAGTCCC AGGCAAACTG GGATGGTTGG TCACCCTGAA 900
GTCAAGACAC CTAGGCTTTG GCACCTAAAC ATCAGTTTCC TCATCTGTAA AATGCTGGGA 960
CTGGCCAGTA CAGCTTCTGA TGTTACTGCC ACATCTAATA GTCCATGATT CACTCTCATG 1020
CTCCTGACCT TACCCATCTG CAGCCCAACT CCCAAACAAA CTTCACTTGA TCCAAGATCG 1080
AGTTCATGTA ACCTGATAAG CTAATCATTA GTGTGTTAAC AGGAGAGGAT TATAGGGTTC 1140
ACAGTTGAAT TTTAACAATG GCTCGGGTGG AAGGCATGTG GGTAGCTGAG TCGTTCTAAT 1200
GGTGGGAAGT TCAGCTGGGG AGATGGAGTG TATGGCTCTG TGCCATCTGA GAGAAAGATA 1260
TTTTTAGGCA GGCAGGTTTT GAGGCAGCCA GCCTGAGAGA GCTGGTTTGA TGGGCTGCTT 1320
TTAGCTGCAC AGCAGGAACA GGCCACAGGC AGGGCAGTCT TGTCTGACTT GAGCCAACTT 1380
TCACACTATG ACCTGAATAA AATCAGCAGT TGAAGCCACA GACTGGAGAA GAAAGGATGT 1440
AGTCTGCTGA TAGCAATATA TATGTATATA ATGCATTTGC TTTGAGCCTG GGTCTGTCAT 1500
CTATAATACA GATATGTAGC TATGATCCTG GGTAGTTGAG AGTTCAGACT CTGGGATCAC 1560
CACCTACCAA CTCTGTGATA TTGGGCAAGT TGTAGACTGA ATAATATGCA TTTGCTGATA 1620
TTTAACCTTT TTGATCTACA CACACAGGAA TTCCACGTGG TTTAGCCTAA TAGCTTACTC 1680
TCTTTTTCCT TGGTTTCCTC ATGTGTGAAA CGCAGATAGC CACCAAACTT TTCAGGACAC 1740
TGTGAGGACC AAATGAGAGG GACACATAAG GTGGTCAGAA CAGTCCTAGC CCCACAGTCC 1800
ATGTCAGTGA TGTCAGCCAC CACCATCCTA CTGGTGAAGA GGCAGGCATA CAGGGCCATT 1860
AGACTCCATC AGCTGAACCT AGGGTAGCCC AGACTCTTCC TGTCTTCCTG AGACATGGAA 1920
CATGGATGAA CCAAAGTGAA TTGGTCACCT TAGCTGAACT GTAGAACTTC ATTCTAATCC 1980
CAGGGTGAGG AAAGGGGAGT AGGTTCATAC CACAGGTTTT TCAGGTCATT CCAAGACTGA 2040
ATGTTTGTTT TTCCTCCCAA TACAATCAGG TCCTAAGTAT AAAAAAGAGC TTTTTATCAT 2100
GAGGTTTTGC TCTAACACCA TGGAGCCCTT TCTTTAGCCT TACATCTGTC TGTAGCGCCC 2160
ACACATGGCC GTCTTCTTCA ACTTAACTAT ATACACACAC ATACGCATAC ATTGTGAAGC 2220
ACATAAGGAA CACATGAGAC AGCCTCATCA TTATCAGATT ACAAAAAAGT TACACTGAAT 2280
TTCTTCTCTC AATAATTAAC AGGGAGCAAT TCAAAAAGAG GAAACAAAAC 2330
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