Tag | Content |
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EnhancerAtlas ID | HS108-21024 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr19:51110560-51112110 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CREB1 | MA0018.3 | chr19:51111400-51111412 | AGTGACGTCACC | + | 6.22 | CREB1 | MA0018.3 | chr19:51111400-51111412 | AGTGACGTCACC | - | 6.22 | EBF1 | MA0154.3 | chr19:51111886-51111900 | TGTCCCTGGGGACT | - | 6.15 | RFX1 | MA0509.2 | chr19:51111546-51111562 | TGTCATCATGGCAACC | + | 6.25 | RFX1 | MA0509.2 | chr19:51111546-51111562 | TGTCATCATGGCAACC | - | 6.25 | RFX2 | MA0600.2 | chr19:51111546-51111562 | TGTCATCATGGCAACC | - | 6.2 | ZNF263 | MA0528.1 | chr19:51110877-51110898 | CGCTCCTCCCCTGCCTCCCTC | - | 6.24 |
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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 |
GH19I050608 | chr19 | 51111341 | 51111570 |
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Enhancer Sequence | ACCTTGCCTG GCCGTCTCTC CCGTATTTCT TAGACCCCTT CATCTCTGTC CTGGCCCCTG 60 GGATCTTTGT CTTCGTCACC TCTCTAGTTC GCTCCCATCT GATTCACTGT CTTCTCTCTC 120 TGGTCCTGTC CCCTTTGCCT ACGAATGTAT CCTCTTTATT GCTGTTGATC CCACTGCTGC 180 ACTGTCCTCG CTGCTGCCTT CTCACAGTCC TGTCGCCGTC CCCATCCTCT TTCTCAGTCC 240 CCTGTGCCGT CGGGCGCTCC ACCTGTGACC GTGGGGTCTT TTTCTGTCCC CTCGGTGCCT 300 GTCACAACCC CTCTTGTCGC TCCTCCCCTG CCTCCCTCGC CTCAGGGCCC TTCCCCGTCT 360 CCTTCTCTTC CTGTCATCCC TGGCTCCTTC CCAGCGTCTT TTCTTCCTTC TCCGAATCGT 420 CGTCTGCTCC TCTGGGTTTG CGGCTGTTGG GGACTCTGCC CCTGGGAGAG AGAAATGCGA 480 AACGTATTTC TGGGAGCTGG AAGCTGTTTC CTCCATTTAG TCTCTGGATG TTTTCTAGGT 540 GACCACAGCC TCTTATAGGC CTGTCCTGGG GCAGAGCGGC CACCTTGAGG TCCATCAGTC 600 AGTCTGATCA TCTCTGTAGA ACCTCGAACC TCTCGCCTCG CCTCGCCTGA CGCCGTTTCC 660 TGCCCTTTAT CTCTCCCTTC AGAATTAAAA AAAAAAAAAA AAAAAAAGAC AGTCGGAAGC 720 AGCAGCGCAT GAGCCCCAAT CACCACTCTG AAACAGGTGC GCGCGGTGGC CTGCGGGCTC 780 GCGGGAGCTC ACGCGAACTC ACGCGCGAGC TCACAAGCTG CGGCGGCCGG CTAGGCGACT 840 AGTGACGTCA CCGAGGCTTG TCCCTGCCTT ATTGGCTGCC TTCGACCAGC GCGCGTTTGC 900 TGGAGTAGTC GGCCACGCCT TGCCAATCGC CAGGGGGCGC TCAGCGCTAG AGCTCCGCGA 960 CCCTGGGAGC CCTATAGAGA GACTCGTGTC ATCATGGCAA CCCTGCCCTA CCTAATTGGA 1020 TACCTGCTCC AGTTGGTTGG ATCCATTACT CTGATTGGAT GCCTGGCGAG TCAAGGCTTG 1080 TATATAATTG GATGCCGGAA ATTTGGATCT TTTCTACGTT TCGCATTTCT GTCTCTTAGC 1140 CGGATTTCTT CCGCAAGCAC TGGGGATGTG GAGATTGAAA GTAACTTGAG TCTCCGTGGG 1200 GGAGTGATGG GTGTTGGGCA CGGTATGGGA ACCTGGCCCG AGTCTGCGGA CCCGATTGGC 1260 TGCTGTCTCT CAGATACAGG TCCCTTTCGT CCCGCCAAGG GGGGCCATGG AACGTAGGGC 1320 CCTCTCTGTC CCTGGGGACT GGGTGATGTC AGGGGTGATT GGCTACATCG CTCCCCAGAA 1380 GGTGAAATGG AAAAATTGAG AGCACTTTCC CACCAGCTTC GGTGGCTCCA TCAGGTTGTC 1440 CTGGCGCACA AGCTGGCGAT GCTATGTGTT TGAAGCTAAC CTGGGCAAAA TTGAAAAAAA 1500 ATTGTTTTTT CATTGTTCCG TCATAAAGGG AGGTCTCGAC AGGAAGAAAT 1550
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