Tag | Content |
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EnhancerAtlas ID | HS183-02094 |
Organism | Homo sapiens |
Tissue/cell | T47D-MTVL |
Coordinate | chr17:36476650-36478000 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HES2 | MA0616.2 | chr17:36477780-36477790 | GGCACGTGCC | + | 6.02 | HES2 | MA0616.2 | chr17:36477780-36477790 | GGCACGTGCC | - | 6.02 | Nr2f6(var.2) | MA0728.1 | chr17:36477357-36477372 | AAGGTCAGGAGTTCA | + | 6.04 |
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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: 2 | ID | Chromosome | Start | End |
GH17I038320 | chr17 | 36475974 | 36477600 | GH17I038324 | chr17 | 36477941 | 36478090 |
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Enhancer Sequence | GGTAGAGGCA CTCGTCTGCC TTCCTCCCAG CTTTTTTTCA CTCTGAGCTT GGGCACCTCC 60 CTCTGGAGTG CTGGGTATGG TTGCCCAGGA CTGTAGACAG TAATAAAAGG TACACTGTGA 120 TCTGTCTTCC TTGCTGTGCC GCTGTCCCCT TCCCACTGTT ACATGTTGGC TCTACTAAGA 180 TGTGTGAGGA TATTCTCTCC CACTCTTCCT GATTTTTTTT TTCCCCCAAG ACAGGGTCTC 240 ATTCTCTCAC CCAGGCTGGA GTGCAGTGAT GTGATTGTGG CTCACTGCAG CCTCAACCTC 300 CTGGGCTCAA GCAATCCTCC CACCTCAGCC TCCAAGTAGC TGGGACTACA GGGGCACGCA 360 ACCATGCCTG GCTAATTTTA GTATTTTTTG TAGAGACCAG TCTTGTCATT TTGCCCAAGC 420 TGGTCTCAGA CTCCTGAGCT CAAGTGATCC ACCCACCTCA GCCTCCCAAA GTGCTGGGAC 480 TATAGGCATG AGCCATTGTG CCCCACTCCT TCTTGGTCTT GACTTCCCCG TCTCTCTGCC 540 CCCTGTCAAA GAACTTGTAA GAATAAAGTG TCAGTAGTTG ATCAGATAGT CCTAGATTCA 600 GAATTCCGAG ATAACTTTTT TTCTACCCAT TAAGATTTTT TCTGGCTGGG CACAGTAACT 660 CATGCCTGTA ATCCCAGCAC TTTGGGAGGC CACGGCAGGC AGATCACAAG GTCAGGAGTT 720 CAAGACCAGC CTGGCCAACA TGGCAAAACA CTGTGTACAC TACAAATAGA AAAATTGGCC 780 GGGCATCATG GTGTGTGCCC GTAGTCCCAC CTACTCAGGA GGCTGAGGCA GGAGAATCGC 840 TTGAACCTGG AAGGCGGAGG TTGCAGTGAG ACGATACCGT ACCACTGCAC TCCAGCCTGG 900 GCAACAGCAA GACTCCGTCT CCAAAAAAAA AAAATTTAAA AAGATTTTTC TTATGGTGGT 960 TTCAAAAATG GTTGTGTGGC AGGCTGGGTG CAGTGGCTCA CGCCTGTAAT CCCAGCACTT 1020 TGAGAGGCCG AAGCGGGTGG ATCACCTGAG GTCAGGAGTT GGACAGCTGG GTCAACATGG 1080 TGACACCCCA TCTCTACTAA AAAAGACCAA AAAAATCATC CAGGAGTGGT GGCACGTGCC 1140 TGTAATCCCA GCTACTTGGG AGGCTGAGGC AGGAGAATTG CTTGAACCCA GGAGGTAGAG 1200 GTTGCAGTGA GCTGAGATCA TGCCACTGCA CTCCAGCCAG GGCAACAGAG TGAGACTCTG 1260 TCTCAAAAAA AAAAAAAAGG TTGTATGGCA ATAAAACAAA CAACTCACAC TCACACACCA 1320 AAAAAACTAA GAGGCCAGAT TTGCTTTTAT 1350
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