| Tag | Content |
|---|
EnhancerAtlas ID | HS093-15131 |
Organism | Homo sapiens |
Tissue/cell | HL-60 |
Coordinate | chr19:13023650-13025940 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ESX1 | MA0644.1 | chr19:13023797-13023807 | ACCAATTAAC | + | 6.02 | | Nr2f6(var.2) | MA0728.1 | chr19:13025641-13025656 | TGAACTCCTGACCTC | - | 6.22 | | RREB1 | MA0073.1 | chr19:13025331-13025351 | CCCCCCCACACCCCCCATAA | + | 6 | | ZNF263 | MA0528.1 | chr19:13024785-13024806 | CCCTCCTCTCACTCCTTCTCC | - | 7.48 | | ZNF740 | MA0753.2 | chr19:13025327-13025340 | CCACCCCCCCCAC | + | 7.52 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH19I012911 | chr19 | 13022750 | 13026005 |
|
Enhancer Sequence | CTGCATCAGA TGTCTGCTGA GAGCTTCTTT ATTTTTCCAA CCTCTCCTTT GGGGATTTAT 60
CCCTTTTGAT TTCATTTTTC TTAATACACA GCAGCTGCAT ATTAATCAGG ATGCTAATGA 120
ATCATAGGCT TCCCTGGGCC TGCATTCACC AATTAACTTT AACAAACAAA ATGCGTGGTG 180
TCCTCTCTGC TGGCTTTCCC GGTTCCTAGG CTGGCTTCTG TTGCCGAACC CTGGACCGAG 240
GCCAGAGAAT GCAAGTCAGC CCAACACAGC ACGTCGGGTG TGCATGGCCT GCGCCCGGAT 300
TGGGCAGCGG GCTGGGGGCT GTGAACACAG CGCTGCGTTC ATCTATTATG GTCTGTCCTT 360
CTAAGAAGTC CCTAATTTGG CTGCGAGGAT TAGGACATAG TTCCCAAGCA GGGCCCACGC 420
TGGCAGGGGG CCCAGGAGCT GCGGAGGAAA TGGGTCTAAG CGAAGAGACC ATCTGTTCGC 480
TCCAGGTAAA GCTGTGATTG GCAGGCGACT GAGCCAGAAC TGCCCGCTGG TGGGGCCCTC 540
CCTCCGTGGC CTCTAACAGA TATACAAGTA AACAATCCGC CAGCCACTTA TGACCACCGA 600
GGGTGGCAGT CCCGGGAGAG GAGGCAAGCT AATCAAACAT TCAAGGGGGG AACACAACAG 660
AATCTCTGGC GCTTGGGCAA AACAATGTTT TGCTGAAGTA CAGCCAGGAA GGGGGAAGGT 720
TTGAATGGAA GCTGATGAGC CAGTTCCTCA ACCTCTCCTT TTCTCTCTGG AAACGTGTTA 780
ACATTTTAAT CATGTTGCTG AGTATCTGCT GCTGGATCTA TTAACTGGCC CCTGCACTGG 840
TTTTAATCTA TCTGTTTTTT GGCCCAGGGT TCCTGTGGAG CTCCTTGAAG TCTCTAAATG 900
ATTTGCAGCG GTCTGTGTCT CTTCACTACA CAGATCCTGG TCTAAACATG CTATTCCGCA 960
GTAAGGTATT AGCAAACAAA CGACTTCAAC CATTGCTTCC CTTTTTTTTT GGTCTCCAAT 1020
TGACAGCACA CACCTATAAA CCATTTCACG CGTGGCCTGC TTTCCAGCAG AGGAATGTGC 1080
GAGGAGAGGG AAGCTGGCTT GCTTTCTGCC TAGAGTCCTC AGGGCCCTGT CCTGACCCTC 1140
CTCTCACTCC TTCTCCAGGT GAGCTCATTC ATTCCACAGC TGCTGCTGAA ACAATGACTC 1200
CCACAGAACC ATCTCCAGAC CCTCACCCCA CCCCGAGTTC CGGGTCAGAA AGTTGAACTG 1260
TATCCTGGAC ATGTGGATGT CCCTGGCCAC CGAAAGTGGC TCAGATAAAC AAGGACAACA 1320
CAGAACTCAT GTTCTTGTCT CTGCCAGAGA AGCCACCACC TACCGGAAAC CACCACAAGC 1380
TGGAAAGCAG ACAGCAGTGA TGTGCTTGTA AGCATTTAGC AACTGGCTGT GTGATGGGGG 1440
GGAAGCCCTG ATTCGTAGTG TTTGCCAATT TCCGTGGTGC AGAGCCTCCC ACCATTAGCC 1500
AATTTCAGGC TACCAACATG AAGACGCTAA ATGCCAAGTT GGGAAGAGAT GTGTAGAATT 1560
GGCTCTTTCA AGCCGGTAGG AGCTGGCCCC AGTACATCAT GGCCGGGAAA CATCCTCCCT 1620
CATCCCCTTC CTGTGTCTTA TGGCACAAGG CACTTCCTCC ATCTGCCCTG CTAAAGGCCA 1680
CCCCCCCCAC ACCCCCCATA AAAGCCTCCC ACTAGACCTC CCTACACCCA CACATTCTCC 1740
CTCCCAACCA TTCTCTACAA AGCAGCCATA TTTTTTTATT AATATTTTTT GAGACAGGGT 1800
TTTGTTCTTG TTGCCTAGGC TGGAGTGCAA TGGTGCAATC TTGGCTCAGT GCAACCTCTG 1860
CCTCCCAGGT TCAAGCGATT CTCCTGCCTA ACCCTCCCAA GTAGCTGGGA TTACAGGCAT 1920
GCACCACCAC CCCTGGCTAA TTTTGTATTT TTAGTAGAGA CGGGGTTTTG CCATGTTGGC 1980
CAGGCTGGTC TTGAACTCCT GACCTCAGGT GATCCATCTA CCTCGAACTC CCAAAGTGCT 2040
GGGATTACAG GCATGAGCCA TCGTGCCCGG CCTGCAGCCG TATCTTTTTA TAACGGGAAC 2100
CTGAGCATGT CACTTCTGTG ACCCAGCAGT TCCCCTCCTA GGTATGAGTA TGCCCAGAAG 2160
AAATGAAATC ATCTGTCCAC ACACAAACTT TTCTAAATGG ATTTCATAGC AGTGCTGCTC 2220
ATAATAGCCA AAAAGTGAAA ACCACCCGAA TGACTATCAA CAGATGAGTG GATAAACAAA 2280
ATGTGGTAGA 2290
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