Tag | Content |
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EnhancerAtlas ID | HS060-19785 |
Organism | Homo sapiens |
Tissue/cell | GM12891 |
Coordinate | chr2:99163470-99164890 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NR2C2 | MA0504.1 | chr2:99164511-99164526 | AGAGGTGAAAGGTCA | + | 7.07 | Nr2f6 | MA0677.1 | chr2:99164512-99164526 | GAGGTGAAAGGTCA | + | 6.6 | Rxra | MA0512.2 | chr2:99164512-99164526 | GAGGTGAAAGGTCA | + | 6.8 | TCF3 | MA0522.2 | chr2:99164213-99164223 | AGCAGGTGTT | - | 6.02 | ZNF263 | MA0528.1 | chr2:99164678-99164699 | GAGGGAGGAGAAACAGGGAAG | + | 6.12 | ZNF263 | MA0528.1 | chr2:99164681-99164702 | GGAGGAGAAACAGGGAAGGGG | + | 6.13 |
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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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Enhancer Sequence | CAGTCAGTTG AGCACCATAG GCATCGAGCC TGGAGCATGT TGTTTCCTAG AGGACAGCAG 60 TGGTAAACAT TCCCAGTTTT TGAAACATTC AGGGGGCTGT ACAGAGCTAC TGTCCTGAGC 120 AGGAAATTTC CAGGTAGGGA GGGTGGTGAA GGGCATTTCA GACAAAGACA TGGCAGAAGC 180 ATTGCACATG GTGAAATGTG GCCAGGTGCA CAGTGCTGGG GGCGGAGAGC TAAGAGGACT 240 GGCCTTGCTG CCAGCCTGCT CTGTGACCAG AGTTACAGCC CCCAGCAGAT CTAGGCCTGG 300 TTCCAGGAGC TCAGGGCCTT GCCTGGGAGT AGACAAGTCA GCAAGCACCA TTTGGCATGA 360 ACAGGGCCTG AAACAAGCAT GCTGAGGATG CTGGGGTGCA TGGAGCAGGG CATCCACCCA 420 GCCCCCAGGG GTGGGAGGGA GAGAGCCAGA AATAAACCCA AGCTGTTGTG TTAGATGTGC 480 AGGAGGCATT GATGATCTTC CAGAACATCA CCTGTGAAGA TTTCAGTGGC TCAGGAAGTG 540 GGGGTGATGA GTGTAGATGA CCAGTAAGAT CCTTGGACTG TGACCACAAA GTAGAGGAAG 600 TAGCATGAGG TGTTTGGTTT AGGGAGAATA ATTATGACTT AGCATGTGTT TGGGCTGATA 660 GGAAAGACAG AAGTGGATGA GGTAAGGTGA ATGAGAGGAA AACAGTGTTA GAGCCGGGTT 720 CTCACAGGAT GGAAAGAGGC AAGAGCAGGT GTTCATCAGA AGGGCCAGGA GAAGAGGTGG 780 GGCTGCAGAG AGATGTTTGA GGTGGGAAGG AACAAGCAGA AGCATCCGTC GACAGCCTCT 840 GCAGCATGTG GGCTGGGGAG GGTCAGACTC AGCAAGCAAG CATGGAACAG CGTGAGGGAA 900 GGTGAGCAAA GGCCCAGGGA GCGTCACAAG AATCCCATGG ATGGTCAGGT GAAGAGCTCT 960 GGCATGTGCC ATGGAGCTGG TGGTTGGCAC CTGACTGTGC TGCCATGGCT GGGAGTCAGG 1020 ACGTGATCTG AGAAAACTGA AAGAGGTGAA AGGTCAGATC AGTGGCTGAG GGGGTCAGGG 1080 AGGCAGCTAG GGGCGTCACT GATCATGGGC AAGGCTGAGC AGGGAACGGA AGAGCGTACC 1140 CTGTGAGAAG TCACCATTCA GATACGTGCA CAGGCTGCCT GGGTGGGCCC AGAGCCCGGT 1200 GAGTCCCGGA GGGAGGAGAA ACAGGGAAGG GGAATTCAGG CCCCCAGACA ACCTACTTGA 1260 CTTTGATTCA TTCCCAGGGG TGCTTCCCTA AGACAAACCA GGTAACCAGA CCTGTCTTAG 1320 GATTTGCTGA CTCCAGGTCC CTTTGGGAAA TAGGAAGAAG ACGCAGCTTC CTGTGCCACC 1380 GCAGCTCTGC ACAGCCAGCC AGAAAGCGTG TCTGTCGCTC 1420
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