Tag | Content |
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EnhancerAtlas ID | HS187-00252 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr1:16746690-16748000 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF2 | MA0051.1 | chr1:16747394-16747412 | TGAAAGTGAAACCCATCA | + | 6.39 | RREB1 | MA0073.1 | chr1:16747211-16747231 | GGGAGGGTGGTGGGTTTGGG | - | 6.21 | RREB1 | MA0073.1 | chr1:16747212-16747232 | GGAGGGTGGTGGGTTTGGGG | - | 6.64 | ZNF263 | MA0528.1 | chr1:16747931-16747952 | TCTTCCTCCTCCTGATCCCCC | - | 7.03 | ZNF263 | MA0528.1 | chr1:16747928-16747949 | CCCTCTTCCTCCTCCTGATCC | - | 7.17 |
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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 |
GH01I016420 | chr1 | 16746901 | 16748580 |
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Enhancer Sequence | GTTGCGAGGT GGGCTCTGTA AGGACAGAGC TCTTCCATTT GATAAGCCAG ATGGAGATTA 60 TGGAGACCCC GATAAAAGCT CTCATATGGG GATGTGTTGA GAAAAGACAA GCGGAGGAGG 120 TGAGGGGGAC AATTATTGAG GGATGGGGCT GCAAAGGGGA GCAAGGAAAG ACGGCTTTTG 180 ACGCCAGGTA TGTTTGTACA CGCCTGTAGT CCCAGCTACT CAGGAGGCTG AGACTAGCTT 240 GAACCCGGGA GGTGGAGGTT GCAGTGAGCC GTGATCACAC CACTGCACTC CAGCCTGGGC 300 AACAGAGACT CTGTCTCAAA AAAAAGGAAA GAAAGAAAGA AAGGCAGCTT TTGATATTGT 360 GGAGGCTGAG CCATGTTTGT ATGCTGATGG AATCGTCCTG TAGTAACGCA GAGAGGGATC 420 ATGTGGTGGG GGGAGGGGAC GAGAGCTAAT GAATAAATGG GGAGACAGCC ATGGGAGCAG 480 GGGCCCATCT TCACAGCTCC CATTGCAGCC AAATCAAGGC AGGGAGGGTG GTGGGTTTGG 540 GGATGCTTCT TCTCATCTGA TGCTTCTGTT TGTCAGTGAC ACATGAGTGA GATGAGGGGC 600 GTGGGGGATG CTGTTGTGAA ATGATGACCT GGAGCGGAGG GAGGGCGGTG TGGCCAAGGA 660 AAAGTGAGAC TTGCAGGCAG CATCTGACAT GAGTGGTTAA TGCTTGAAAG TGAAACCCAT 720 CAATAAGACA GGATGTTCTC CAACCGCATT AAGCTGCTCA ACATGGGTAC AAGGCTGAGT 780 GAGTTTAGCC AGGGTGGGGT TTTGCCAATG AACAGAACAG GATGAGACAG GGCAGATGCT 840 GGCAGGGCAT GCATGCTAGT GACTGTGTAT TTGCAGGTTG CCTGGTCAGG TCAAAGAACT 900 AGGAAGTGGC AGAGCTTGGG GAGGGAAGGA TGGCTGGGAG GGGTCGGGGA AGCCTCCCAG 960 GTGTTCAGGG ATGCTTTGGA TTGTGTGGCT GTGGCCGAGG GCAAATGGGT GGAAGAAATC 1020 CATGCTGATG TGGAACAAGC CACCACCTGG GATGAACCCA AGGGCTCCAG AGTGTAAGAG 1080 CATTCTTGAT GCCCACCCAG AATACACACA CATGCATACA CACAGGCACA GGCACACACA 1140 CACACGTGTG CACATCCATG TGCACTTTAA CACACAGCCA CACACACCTT CCTTGGTTTG 1200 ACTCCAAATA GGGGTTTGAC GTGCCACATC CGCTTCTGCC CTCTTCCTCC TCCTGATCCC 1260 CCCTGCCTTT CTCCTACACA GCTCGTCCCC GTTCCCCCTA TGGCCCTACT 1310
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