Tag | Content |
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EnhancerAtlas ID | HS050-44545 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr22:29477550-29478760 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ESX1 | MA0644.1 | chr22:29477732-29477742 | ACCAATTAAC | + | 6.02 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_33639 | chr22:29472764-29479401 | H2171 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr22 | 29477884 | 29478162 | chr22 | 29478277 | 29478419 |
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| Number: 1 | ID | Chromosome | Start | End |
GH22I029081 | chr22 | 29477574 | 29478439 |
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Enhancer Sequence | TGACAATCAG AATTAATCTG TTGGCCACTA TTTGCTCTTA TTCTTATTGC TCCAAGTGAC 60 CAGAGATGAT GGTTCCATCT ACTTATAAAT GAGTGTTACA CTGAGCCTTT CCTTCTGCCC 120 TAAACTGTCT CCCTGGCCAG AACTTATGAA ACCCATCTCT TGAGTCATAT TTTTATGTTG 180 GGACCAATTA ACAAGTACTT ATCAAATTCC TCCTGTGTGC CCAGCATCTC TGATTAGGAC 240 TTATCCCTGT GCCAATTGAC AGAAGGCTAC AACTTTGTTG CTTCGAGTTT TACTTTGAAA 300 TGTGCTCTAG AGATATATGG TCTACCTGGT ATCAGCTCCC CACTCAGGAG CTCTTATATT 360 ATTTGTCTAT CCCATATCAG CCAAGGGAAA CTGAAAAGCC CAGAGTCTGG CTTCCATGGA 420 GTATTGGCTG CCCTCCAGGA CTCTATTATT GGGGAATTTT CTTGCCATCT GACATTAAAA 480 ATAGGTCACA GGCATTACTA ACAAAACTTG TCTAGAAGCT GGATTATATC CAGTTGACCT 540 TCAGACAACA TGGAAAAAGG TTGCTCAAGT GATAGTGAGG CAAGGCGTAG ATTTGAGCTG 600 GGTGCCTCCT GCTTAAAGCA AACTAAGAAT ATAAAATTCA TATTTTTATT TTATTTTATT 660 TTATTTTATT TTTTAGATGG AGTCTCGCTC TGTTGCCCAG GCTGGGGGGC AGTGGCACTC 720 CTGGCCTCAA GTAATCCTCC CACCTTGGCC TCCCAAAGTA CTGGGATTAC AAGGGTGAGC 780 CACTGCACCC AGCCCCCATC CATTTCCTTT AAATAGCAGA GTCCCTGGTT TAAATAGCAA 840 ATATTTGATT TCCTTGATTT ACATAAACTT GTACTTGATT TACATGAACT TTCCTAGAAC 900 TTCTCATAGG TATTGCTAGG TAAGTCTTGA GGCTGGCCTA GGAGGAATAC ATTGGTGAGG 960 AAACTAATGC ACCCTGAATG TATCTGTAAT GGAGCTTTCC CCTAGCCCCT CATTCACCAG 1020 CTTCCCTCTT TCAACAGACA CTTAGCCAGG CACCTTCTAT GTGGTCTGTA GTTGCTGAGA 1080 ATACAAAGGT GAGTAAGATG CTCACAGGCT ATTGGAAACA GGGCTATGTG CTTCCTGAGC 1140 AGTTACACTT CAAGGTAATC AAGTCCTTTA AGAGCTGTGG CAGCAGGCAC TGTGACTTGT 1200 TTCAAAACCT 1210
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