Tag | Content |
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EnhancerAtlas ID | HS104-28761 |
Organism | Homo sapiens |
Tissue/cell | HUVEC |
Coordinate | chr19:8431840-8433360 |
SNPs | Number: 2 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr19:8432550-8432568 | CCATCCTCCCCTCCTCCC | - | 6.25 | ZNF263 | MA0528.1 | chr19:8432553-8432574 | TCCTCCCCTCCTCCCTCCCTC | - | 8.11 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_31774 | chr19:8431216-8432883 | Gastric |
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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: 1 | ID | Chromosome | Start | End |
GH19I008365 | chr19 | 8430485 | 8433586 |
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Enhancer Sequence | TCCGTTCATC TCGAACCACA GCATGTCCAC GTGTGTCCGA TGCAGACTCG CGGTTCTCTA 60 AGTTCACGGC CCCACACGGT TTCTCTGTGG TCCTCATCCT TCCCTGCATC TGTGGCTGTC 120 CACAGCCAAC TGGGTGAAAG TTTGGATCCC CCTCTCACAC CCTAGGGTCA GTGGCAGGCT 180 TCCAGCACTG TAGACCTGAG GGTTCTCTCC TCCCCAAGCT CCCGCTCCTT CCCACCTCCG 240 TGCTGCCCGC CCCCAACCCC GCCAGGCTAG CATCTCAGCG TGGTCAGGGT CCTGTCCACC 300 CTCCCAAAGC CACCATCCCA GGATGAGGGG CTTCTGGAGG GTGACGGGGG AAGGCACAAG 360 TCCTGGCTGG GAAATGCGGT GGAAGGGGGC AGGGGTTCTG TGGGTTCGGG ACTCCCAGAC 420 TCTTGGCTCA GGCCCGCCAA GTAGGAGAAA GTTCAGAGCT GGGAAGGCGA ACAGCTGGCA 480 TTCATGGAAG CCACACTGGT GGTTTGGCCG CGTGCCCATC CTTACTGGAT GGGAGGAAAG 540 TAGGGGAAAG GGGAGATGCC TGAGGGGCCG GAAAGCGTCT TCCTGGTCAC TCTGGGCCCG 600 CCCCCACCCC CACCGTGCAG ACTCATTTCG ACCTTTCCCC TACTTTTCCG GCTGGGCTGG 660 GGGCGGTTCC TCCCAGTCTG GAGCGTCTGA GCCTCCAGAC GTGCTCAACG CCATCCTCCC 720 CTCCTCCCTC CCTCTTTCTT TCCTCAACCC TGCCTCCTCT CCCTCTAGGA GCTGGGACCC 780 CAGGCAGAGC CTCTGAGATG CTCCTGCTCA GCACAGTTCT TCCCGTTCTG GACCTGCTGC 840 CTCATTCATT CATTCATTCA TTCATTTGTC AAGACTGTTT TGTTTGCTTT TTGAGACGGA 900 GTCTCGCTCT GTTGTCCAGG CTGGAGTGCA GTGGCGCAAT CTCAGCTCAC TGCAACCTCT 960 GCCTCCCACT GGGTTCAAGT GATTCTCCTG CCTCAGCCTC TCAAGTAGAT GGGATTATAG 1020 GCGCCTACCG CCACCACGCC CAGCTAATTT TTATTCATTT ATCAAGTCTT TTTTTTTTTT 1080 GAGACAGAGT CTCACTCTGT CACCCAGGTT GGAGTGCAAT GGTTCAACCT CAGCTGACTG 1140 CAACCTCTGC CTCCCGGGTT CAAGTGATTC TCCTGCCTCT GCCTCCTAAG GAGCTGGGAT 1200 TACTGGCGTC CACCATCACA CCCAGCTAAT CTTTGTATGT TTTACTAGAG ATGGGGTTTG 1260 GCCATGTTGA CCAGGCTGGT CTCAAACTCC TGACCGATCC GCCCGCCTCC CAAAGTGCTG 1320 GATTACAGGC ATGAACCACT GCGCCCGGCC CATTCCTCAA GTCTTTATTG AGCAGCTGCT 1380 ATGCGCTGGG GCCTGCGTGG ATGCTGGTGC CAGGCTGTGG GCAGAGCTGC TCCTTGTCCC 1440 CAGCCTCATG GAGCCTCCAT TGAGTCAGAG GAGAGACCAT TAGATGACCT CAGTGTCCAG 1500 GAGTGGGAAG TCCTTGCTCA 1520
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