| Tag | Content |
|---|
EnhancerAtlas ID | HS029-07626 |
Organism | Homo sapiens |
Tissue/cell | CUTLL1 |
Coordinate | chr19:13023730-13026040 |
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 | TTAATACACA GCAGCTGCAT ATTAATCAGG ATGCTAATGA ATCATAGGCT TCCCTGGGCC 60
TGCATTCACC AATTAACTTT AACAAACAAA ATGCGTGGTG TCCTCTCTGC TGGCTTTCCC 120
GGTTCCTAGG CTGGCTTCTG TTGCCGAACC CTGGACCGAG GCCAGAGAAT GCAAGTCAGC 180
CCAACACAGC ACGTCGGGTG TGCATGGCCT GCGCCCGGAT TGGGCAGCGG GCTGGGGGCT 240
GTGAACACAG CGCTGCGTTC ATCTATTATG GTCTGTCCTT CTAAGAAGTC CCTAATTTGG 300
CTGCGAGGAT TAGGACATAG TTCCCAAGCA GGGCCCACGC TGGCAGGGGG CCCAGGAGCT 360
GCGGAGGAAA TGGGTCTAAG CGAAGAGACC ATCTGTTCGC TCCAGGTAAA GCTGTGATTG 420
GCAGGCGACT GAGCCAGAAC TGCCCGCTGG TGGGGCCCTC CCTCCGTGGC CTCTAACAGA 480
TATACAAGTA AACAATCCGC CAGCCACTTA TGACCACCGA GGGTGGCAGT CCCGGGAGAG 540
GAGGCAAGCT AATCAAACAT TCAAGGGGGG AACACAACAG AATCTCTGGC GCTTGGGCAA 600
AACAATGTTT TGCTGAAGTA CAGCCAGGAA GGGGGAAGGT TTGAATGGAA GCTGATGAGC 660
CAGTTCCTCA ACCTCTCCTT TTCTCTCTGG AAACGTGTTA ACATTTTAAT CATGTTGCTG 720
AGTATCTGCT GCTGGATCTA TTAACTGGCC CCTGCACTGG TTTTAATCTA TCTGTTTTTT 780
GGCCCAGGGT TCCTGTGGAG CTCCTTGAAG TCTCTAAATG ATTTGCAGCG GTCTGTGTCT 840
CTTCACTACA CAGATCCTGG TCTAAACATG CTATTCCGCA GTAAGGTATT AGCAAACAAA 900
CGACTTCAAC CATTGCTTCC CTTTTTTTTT GGTCTCCAAT TGACAGCACA CACCTATAAA 960
CCATTTCACG CGTGGCCTGC TTTCCAGCAG AGGAATGTGC GAGGAGAGGG AAGCTGGCTT 1020
GCTTTCTGCC TAGAGTCCTC AGGGCCCTGT CCTGACCCTC CTCTCACTCC TTCTCCAGGT 1080
GAGCTCATTC ATTCCACAGC TGCTGCTGAA ACAATGACTC CCACAGAACC ATCTCCAGAC 1140
CCTCACCCCA CCCCGAGTTC CGGGTCAGAA AGTTGAACTG TATCCTGGAC ATGTGGATGT 1200
CCCTGGCCAC CGAAAGTGGC TCAGATAAAC AAGGACAACA CAGAACTCAT GTTCTTGTCT 1260
CTGCCAGAGA AGCCACCACC TACCGGAAAC CACCACAAGC TGGAAAGCAG ACAGCAGTGA 1320
TGTGCTTGTA AGCATTTAGC AACTGGCTGT GTGATGGGGG GGAAGCCCTG ATTCGTAGTG 1380
TTTGCCAATT TCCGTGGTGC AGAGCCTCCC ACCATTAGCC AATTTCAGGC TACCAACATG 1440
AAGACGCTAA ATGCCAAGTT GGGAAGAGAT GTGTAGAATT GGCTCTTTCA AGCCGGTAGG 1500
AGCTGGCCCC AGTACATCAT GGCCGGGAAA CATCCTCCCT CATCCCCTTC CTGTGTCTTA 1560
TGGCACAAGG CACTTCCTCC ATCTGCCCTG CTAAAGGCCA CCCCCCCCAC ACCCCCCATA 1620
AAAGCCTCCC ACTAGACCTC CCTACACCCA CACATTCTCC CTCCCAACCA TTCTCTACAA 1680
AGCAGCCATA TTTTTTTATT AATATTTTTT GAGACAGGGT TTTGTTCTTG TTGCCTAGGC 1740
TGGAGTGCAA TGGTGCAATC TTGGCTCAGT GCAACCTCTG CCTCCCAGGT TCAAGCGATT 1800
CTCCTGCCTA ACCCTCCCAA GTAGCTGGGA TTACAGGCAT GCACCACCAC CCCTGGCTAA 1860
TTTTGTATTT TTAGTAGAGA CGGGGTTTTG CCATGTTGGC CAGGCTGGTC TTGAACTCCT 1920
GACCTCAGGT GATCCATCTA CCTCGAACTC CCAAAGTGCT GGGATTACAG GCATGAGCCA 1980
TCGTGCCCGG CCTGCAGCCG TATCTTTTTA TAACGGGAAC CTGAGCATGT CACTTCTGTG 2040
ACCCAGCAGT TCCCCTCCTA GGTATGAGTA TGCCCAGAAG AAATGAAATC ATCTGTCCAC 2100
ACACAAACTT TTCTAAATGG ATTTCATAGC AGTGCTGCTC ATAATAGCCA AAAAGTGAAA 2160
ACCACCCGAA TGACTATCAA CAGATGAGTG GATAAACAAA ATGTGGTAGA CTCATGTGGA 2220
ATATTATTCA GCCATTGAAA AGATGAAGTC CAGATGCAGT GGCTCACGCC TGTAATCCCA 2280
GCATTTTGGG AGGCCACTGT ATCTGGCCTG 2310
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