Tag | Content |
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EnhancerAtlas ID | HS104-01488 |
Organism | Homo sapiens |
Tissue/cell | HUVEC |
Coordinate | chr1:39318160-39319420 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Mecom | MA0029.1 | chr1:39318279-39318293 | CTTTATCTTGTCTA | - | 6.02 | NKX2-5 | MA0063.2 | chr1:39319194-39319204 | ACCACTTGAG | + | 6.02 |
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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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Enhancer Sequence | CTGAAAAACA CAACATAGCT TGATTAATTT GAAAAATACC TTATGTTCTA TGACAACTAT 60 TATAATACAT AAAATTTTAA GTTTCTTAAC ATTTGATTTC AGTGAGTTCA ATAAAGCCTC 120 TTTATCTTGT CTACCATACC CATCACTCAA GATGACAAAT ACACTTTCCC ACCTGGCTTC 180 ATCTCTTTAC TGCATTTACA CAGGGGGCAA CTGAAGTAGT ACTGAGAAAA GGATTTTCAG 240 GTACATAAAC TCCAATATTC ACCGAAGTCT TTGCAATCTG ATCCAAAAAG CTTTTTTTAA 300 GCACATAACT GAGACCAAAA ATAAGACTAA AACCGAGAAA ACTAGAAGAG TTATGTGACA 360 TTTATTAAAT AAGAACATAA TTCAGGTTTC TACTAAAATG TCACCTCAAA AAGTTCTTTC 420 CAGACCAGCC TACCTAAAAT AGCACTCGTG TACCCAAGGC TTTCAACCCC TTTCCCCTAA 480 TTTGTTTTTC TTCACACCAC TGGTAAGTAC TTAAAACGAT ACTATACATT CATTTAGGTG 540 CTTCTGAGCT GTGTCACTGA AAATGTTAAG TTCCAGGGGA AAGAGACTTT GTCAGTCTCG 600 CTCCTAGCAG CAAGCCCACT TCCCTGAACA GTGCTCATAA GTATCTGCTG AATAAACAAA 660 TGAATACAAT TGGTGTTTAC AATTTATGTA AAGAGCATAT TAAACAGGAT GGGAGTCGGG 720 ACTCTACAGA GAATGGAGGA ATCTACAGGA GTCTGGAGGC CTAAAAGGAC TTACGGTGGA 780 GAAGTAACAC ATGTAGATTC AATAAAACAC GTATTTGAGA GGGAAGCCTT TAACAATTTA 840 AACACTGTCA ACAATTCTAT CTGCTTTATA ACTCAGGGAG TACAATCTTC ATTATATAGT 900 CGCATCCACC ACACATTTAT ACGTATATAT AACATCAGAG ACACAGAACT TTATAGGTAA 960 TTTAAAGATA CTTTCAGCTG GGCGCGATGG CTCACGCCTG TAATCCCAGC ACTTTGGGAG 1020 GCCAAGGCAG GTGGACCACT TGAGGTCGGG AGTTCGAGAT CAGCCGGACC AACATGGAGA 1080 AACCCCATGT CTACTAAAAA TACAAAAAAT TAGCCAGGCG TGGTGGCGCA TGCCTGTAAT 1140 CCCAGCTACT TGGGAGGCTC AGGCAGGAGA ATCGCTTGAA CCAGGGAGGC AGAGGTTGCG 1200 GTGAGCCGAG ATGGCATCAT TGCACTCCAG CCTGGGCAAC AAGAGTGAAA CTCCATCTCA 1260
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