Tag | Content |
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EnhancerAtlas ID | HS095-21181 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr3:122616900-122618200 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Gata4 | MA0482.1 | chr3:122617348-122617359 | GGGAGATAAGA | - | 6.62 | NFAT5 | MA0606.1 | chr3:122617010-122617020 | ATTTTCCATT | + | 6.02 | NFATC1 | MA0624.1 | chr3:122617010-122617020 | ATTTTCCATT | + | 6.02 | NFATC3 | MA0625.1 | chr3:122617010-122617020 | ATTTTCCATT | + | 6.02 | ZNF263 | MA0528.1 | chr3:122617969-122617990 | GGAGGAGGATGGGTGGGAGGA | + | 7.62 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr3 | 122617285 | 122617508 | chr3 | 122617725 | 122617825 |
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Enhancer Sequence | TATGATAGGT GAACAATGAA AAACTTTCAG GCTTAAAAAT GTATTACATT AAAATAAAAT 60 TCTGTGGGGG AAGTAGAAGG ATACTCCGAG GAGTAAAAGG AACAAAGCAA ATTTTCCATT 120 TGTTCAAGAA TTCTTTCTCT ATTTTTTTAA AACGCTGTAC TTTTTAGATT CTCTTGACTA 180 CATTTTAAAA GAACAGTTAT ATTTTTAAAA TGTCACTATT TACAATATGC CAGAAATTAC 240 ATCTTTTGCA GCTCTTTACA ATGAGAAATT CTAGATGTCA ACGTAAAAAT TGTGAGGGTG 300 TAACTAATGT TTTGGAAATC TTTCAGAAAG TATGTGGTAA AAAAATAATA ATAACAATAA 360 TAGTCTTCTA CCCCACAGTA CTTCACAGAA ACGAACAAGC AGGAACATGT GTGGTGCTGG 420 CTGAGAGCTG GATTCACTCC TCTGAGTGGG GAGATAAGAT GTCCGGGAAC TGGATTTACC 480 TCAGCACATA GACCGTTTAT TTCTGGATGT GGCCCAGGAA AGCAAACACA AATGTGTCAA 540 ACTCCTCTTT TCTCTGAAAG AGAATTTAAA AGTAAAGATC ATAGGCCAAG CCAATGGTAA 600 CATCTTTTGG GCAAAGAATC TCCTTTGTAG GGTATTTGGG TAGAGGGAGA AGTTGGTCCA 660 GGAGAGTGAG TTCTGAGCCA CACCCGTGGA TGTCCATGAG ATAGAGAGCT CCTACAGTTA 720 CAAGAATCAT AGAGTCACTT CAGCCATCAT AAGAAGTGAT TCGACTGGAT ATGGGTTGGA 780 GCCAAGAGGG GGCCAGCTAC CCTTTCTCTC TCTCCCTCCC TGTCTCTCAA TCTCAGCCAG 840 TCCAGTCTTT CTCCCTCGCA GTCTCGGTGT TTCTGCTACA TTCTTCTATT GCTACTAGCC 900 TATCTTATCC TCATTCTTCA GTCCAGATCC CACAGACAGC CACTCTGACT GGCTTAGCTG 960 ATTTCCCTCT GGGCTTTTGG ATAGGGTCCT TCAAGACTGC ACACCGTGGC AGGCAGCCAA 1020 TCTGTAGCCA TCCCTGTGCA AAGACCAGCT CAACACTGCT TGTCTGTTGG GAGGAGGATG 1080 GGTGGGAGGA GCTGTTTCAG AAACCTGGGA GTAATAGACA TGACAAAACC GTGACTGAGA 1140 TGTCCATTTG CCTGTCATTT TCTAGGGTGG AGATGGAAGT CTGGTCTTCC CATGCCCACT 1200 TGTCTCAAGC CCCTCCCACA CATCAAGTGA CAGTAACAGC TTTTCTATCA CCATTTAGGG 1260 ATCATATGGA CATTAAAATG AAGATGAAGA GAACACAGGA 1300
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