Tag | Content |
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EnhancerAtlas ID | HS076-01080 |
Organism | Homo sapiens |
Tissue/cell | H1 |
Coordinate | chr1:23177250-23178740 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MAX | MA0058.3 | chr1:23178645-23178655 | AGCACGTGGT | - | 6.02 | Nr5a2 | MA0505.1 | chr1:23178211-23178226 | CCTGGCCTTGAACCT | - | 6.86 |
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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 |
GH01I022851 | chr1 | 23178080 | 23178304 |
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Enhancer Sequence | AGATGAGGCC CGGAGAGAGG CTCAGGGAAG AACTGATGGA ACCAGGACTT GAACCAGGCA 60 GGAGAAACGG CGCATGCACA GGCCCTGAGG CTAGCAGAAG GCTGGTGTTC TCAGGGCAGC 120 CAAGAGGTCA GTGTGGCTCA GCTGGAGTGG GCAAGAGGCC AGGCGGGTGG AGGGGAGTTC 180 AGAGAGGAAA AAGGAAGCTT TGTAGGCTAT TGTTTTGTGG GTTTTTGTTT CTTTTTGGAA 240 ATTCATCTTT GTTTAGATAC AGGGTCTTGC TCTGTTGCCC AGATTGGAGT GCAGTGGTGG 300 GCTCTCAGCT CACTGCAACC TGAACCTCCC AGGCTCAAGA GATCCTCCCA CCTCAGCCTC 360 CCAAGTAACT GGGACCACAG GCTTGTGCCA CCACGCCCAG CTCATTTTTT AAAATTTTTT 420 TGTAGAGTCA AGGTCTCACT ATGTTGCTCA GACTGGTCTC AAACTCCTCA GCTCAAGCGA 480 TCCTCCCGCC TTGGCCTCCC AAAGTGCTGG GATTACAGGT GTGAGCCACC GTGCCCAGGC 540 TATTGGTTTT TACTCCAAGT GAGATGGAAA CTGTTGGAGG CCTTTGGGCG ACATGAGCTG 600 ATGGCTGTTC TGCAGGATCC TGGCTGCTGT GGAAGGCTGA ATGCAGCTGG AGGAGGGCAA 660 GGACATGGGA GAGCAAGGGA GAAAGCCAGG AAGCCAGTTA GGCTTTTGCC GTGATGTGAG 720 GATGCTCCCA CTCCTCTGCC CCTTCTCTTC CCTCCAATGT GGGCATCAGC ATAGCTGGGC 780 TGCAACCCCA GCTCTGCTGG CCACTCATTT ATTGTGTGAC CTTAGGCAAG TCCCTGTCCC 840 TGTCTGGGTC TTGTATTTTG TAGTCATAAA ATAAGGAACT TAGCCCAGAA GATCGTGAAG 900 ATTCTGCTGA CTTCCAATGT CTGAGACCCT GCCTTACTCT CCAGCCTCAT CTCCTTCCTC 960 TCCTGGCCTT GAACCTCACG TGCTAGCAAC CCTGAACTAT TTGTAGCTCT CTGCACGCAC 1020 ACCATGCTGT TTCACGCCTC TGTGCCTTTG CACACTCCCT CTCCCTGCAA CACCCTGTCC 1080 CAGCAGCAGC CCTGCACACA GATGGCCTGT GTTCTTCAGC AGGTCTCCAG CTTGGGGGCA 1140 TCTCCTCCAG AGGTTGACCC ACTCCCCTTT CTCAGTGCCC TGAGCACTTT TACAGACCAC 1200 ACACTGATTT TCAGAAGACA ATAGAATGAA GAGGCTGTGG AGTCAGAGCT GGCCTCAAAT 1260 TCCAGCTACC TATCTGGAGT TGTTCATGTT TTTGAGCCTC CATGTCCTCG TCTGTGAAAC 1320 AGAGATCATC ATATTCTTCC TCCCAGAGTC AAGGTGAAGA TGCAGCAACA TTGTTAAGCA 1380 CCTACCCCAG TGCCTAGCAC GTGGTAGCCA GGATTTTTGA AGTCAGATTC TAGCTACAGA 1440 GAAAGAGCCA TTGAATGAAT GGGAGAGGGT TACCCTGTAT AGTGTGGCCC 1490
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