Tag | Content |
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EnhancerAtlas ID | HS050-59458 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr6:110617070-110618240 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nkx2-5(var.2) | MA0503.1 | chr6:110617807-110617818 | CTTGAGTGGCT | - | 6.62 | TBX20 | MA0689.1 | chr6:110617964-110617975 | AAGGTGTGAAG | + | 6.32 | TBX21 | MA0690.1 | chr6:110617964-110617974 | AAGGTGTGAA | + | 6.02 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_68364 | chr6:110603711-110620732 | TC32 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 2 | ID | Chromosome | Start | End |
GH06I110295 | chr6 | 110617169 | 110617340 | GH06I110296 | chr6 | 110617541 | 110617803 |
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Enhancer Sequence | TTAATAAAAA CCCTTTGAGT TTACTGAAAA CAATTGAGTG ACTAATTCAC ACCAGGCATT 60 CTGCTGGAGA CTTTCACACT ATGTTCTCAG ACCTACTTCT CAAAAAAAAC CCACAATTTA 120 GAAAGTATCA TTGTCCTCAT TTAACTGACA ATCAAATTGA GTGCCAGAGA GGTTAAATGA 180 CTCGCCCAAC GCCAAAAGCC AATAAGAGGA CCATGCTTCA AACCTAGATT AATGAGCTTA 240 CATAGAGAAA CCCTCAGGCA GCTCTGTTAT TCAGAGTTAT CAGCAGCATG GTTAAGACCA 300 AAAATAATAG CTATAATTCC TCATTAACTA GCTCGGATCA TTGAGGATAC TCTGAATGTA 360 ACAAAGTCTA AAGTAAGAAA GACTTTAGAA AAAAACTATA CATTATGATT AATATGAGCA 420 GAAACTTCAG ATTCAATATT TCTAGTTGCA TTCTGAAAAA ACTGTATGCT TAGTTAACAA 480 TAACCACTTC TGCAAAGAGT AGACAGTTAA TCATTTCACA TAATGCTGGA TCCAAGTGAT 540 ATTACTCCCT GACAGACTGG GCTTCTAATC CACATGGTTT TGCTGATGCA GCTGCTCTAG 600 CCTGATGCTT TAGAACAGGC TTTTGATTTA TAGTTTGAGG TTAAAATTAC CAAAGAGTTT 660 TAAAAGCAGT ACAAAAGCCA TTTGCATCTT TCTGTCACTA TCTCAGAATA CTGCTTTCAT 720 TTTTGCCCAT ATTTTTTCTT GAGTGGCTGG AATCTACGTA TGGATATACA GAATAGGAAA 780 ACTAACAGCG GAATAGGGAA ATTACTACAA AACTATATGA GATATTTTAA AGTTCTGAAA 840 TAAAACAGCT AAAAACGCTT TGGTTTCTAC ACTCACTTTC AGAATAAATG AGTGAAGGTG 900 TGAAGGCAGA AACGCTGACA TTTGTTAGCG TGTTTTTTAC TATTTGCTTC CCCTGCCGCA 960 GCCACATCCT ATTTACCACT GTCTGTACAT ACAGAAAAAT GAAAACAGAT CGTGCTTGCT 1020 ACACGACACA AACAAGGTTT CCATTTATCT AGCCCCGCAT AGCTCCTAGA AGCATTTTCC 1080 TAAGGAAAGC AATCACTCGC TGACGGGTTT AGTTTTGTTG TTTTTGTTTT AAAGCATTCA 1140 CCAAAAAAAA ATCTCTATGG AAGAATATCA 1170
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