Tag | Content |
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EnhancerAtlas ID | HS104-30146 |
Organism | Homo sapiens |
Tissue/cell | HUVEC |
Coordinate | chr19:48629120-48630530 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr2f6(var.2) | MA0728.1 | chr19:48629646-48629661 | GAGGTCAAGAGTTCG | + | 6.24 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_38541 | chr19:48623752-48630434 | HUVEC |
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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 | TGTAATCCCA GCTACTCGGG AGGCTGAGGC AGGGGAATCG CTTGACCCCA GGAGGCGGAG 60 GTTGCAGTGA GCTGAGATCA TGCCACTGCA CTCCAGCCTG GGCAACAGAG TGAGACTCCA 120 TCTCAAAAAA AAAAAAAAAA AAAGATTATC TGGGATATTG ATGATTGCAG CTAATTTTTT 180 TTGAGAGCTT CCATGTACTA ACTACTGAGT TCCACACCCC TATCCCACTG TTTAGCCCTC 240 ACCCTAACAG ATAAAGCACC TGCCACTGTT AGCTCCTTAC TGTAGATCAA GAAACTGACA 300 CACAGAGAGG CTGAGTCATT CATCTGTAGC CATGCCGCTA GGAAGGTTAG GGCTGGGATA 360 TGACGGCATG TGGCCTGGCT CCAGATTCCT GACATCCTAA AGCAAGCTGT TCTCAAACTG 420 TTGTCTTGAG GCCTCTTTAA CACTCTTAAA AATTATTCAA GGCCAGGCGT GGTGGTTCAC 480 GCCTGTAATC CCAGCACTTC AGGAGGCCAA GGTGGGCAGA TCACCTGAGG TCAAGAGTTC 540 GAGACCAGCC TGGCCAACAT GGTGAAACCC CGTCTCTACT AAAAATACAA AAATTAGCTG 600 GACCTGGTGG TGCACATCTG TAATCCCAGC TACTTGGGAG GCTGAGGCAG GAGAATCACT 660 TGAACCTGGG AGGAGGCAGT TGTAGTGAGC TGAGATCTCA CCACTGCACT CCAGCCTGGG 720 TGACTGAGCA AGACTCTTAT CTCAAAAAAA AAAAAAAAAA TTCAAGACTC ACTCCATAGA 780 GCTTGTTCAT GTGGGTTACA TAATATTATA GTTACACCTA TTAGAAATTT AAAATGAGAA 840 ATTAAAAAAA TAAATCCAAT ATGCTCACCC AAATAATATT AATTTTTTTT TTTTTTTTGA 900 ATAGACACAA GGTCTTTTCT ATATTGCCCA GGCTGGTCTT GAACTACTGG GCTCAAGCGA 960 TCCTCCCACC TCCCAAAGTG CTCTGATTAC AGGCGTGAAC CACAGTGCCT GGCTCTAAAT 1020 AACATATTTT GATGAAACAT AACCCAAGTT TTGAGAAAGT GGTGAGACTA GAGGCATTAT 1080 TTTACACTTT TGCAAATCCT CTAATATCTG GCTTAACAGA GGCTGGATTC TCCTGCGTGC 1140 TTCTACGACA CACTCTTCTC GTTGCAGGAC CTGAGGAAGA TCCACCTCAC GCCAATGTGG 1200 AGTTGGAAAG AGAGGGACCT TGAAGATGTC CTTGAAAGAA TCTTAAGGAA CCTCAGGGGT 1260 CCTCAGACCA CACTTTGAGA ACTGCTGCCC AAGTGTGGCT TCCTGGCCAT GTGAAGTGGC 1320 AGAGTCGGAA ATGGAAGTCA GAGGGGCAGC TGCCAGGCTC ACACCCCACC CCGTCACCCC 1380 TCAGCTGCCC CTGGACAGGA AGCTGGAACT 1410
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