Tag | Content |
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EnhancerAtlas ID | HS044-07351 |
Organism | Homo sapiens |
Tissue/cell | Fetal_kidney |
Coordinate | chr2:112663320-112664770 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF1 | MA0050.2 | chr2:112663478-112663499 | AGAAGGAAAGAGAAAGAGAGA | - | 6.4 | PRDM1 | MA0508.2 | chr2:112664023-112664033 | TCACTTTCAC | + | 6.02 | ZNF263 | MA0528.1 | chr2:112663467-112663488 | GGAGAAGGGGCAGAAGGAAAG | + | 6.26 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr2 | 112663535 | 112664666 | chr2 | 112664507 | 112664640 |
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| Number: 1 | ID | Chromosome | Start | End |
GH02I111906 | chr2 | 112663778 | 112664577 |
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Enhancer Sequence | TAGGCGTGAG CCACCGTGCC CAGCCAGAAA CCTACACTCA ATTCTAAAGC ATTTTATTTC 60 ATCCTTCTTG GCTAGTTCTT CAATTATCAG TGCTTCTTTC ACTCAATGGT AAATGGATTT 120 TCCATGAGTC TTGGAGGTGG CAGGCAGGGA GAAGGGGCAG AAGGAAAGAG AAAGAGAGAA 180 CAGATGTTGG CTTTATGTTT GGAATAAAAT TACACCAAAA GCTAAGAACA TTTATATTTG 240 TGCTTAGAGA AACCCCATTT CATTTCAGAA GCTCAATGCC TGGATTTTTT TGCCAGCACA 300 TTTTACACTT GTATGTTTCT CCTTGTACTC TGTGCCTCCA TGTATTTCTG TTGGTCCCTT 360 GAAAACAAGA TCCAATCATC ACAGGGTTAG TGCTCTGCCC TAGGTCACTC CAGTAGGGGT 420 CCATCCTCCG GATTTAGATC TCAGGTTGGC ACTTATGCAA ATGCTTTCTG ACAGGTCCCC 480 TTTTTTGTGT AATCTGCTTT TTCTTTGAGG ATCTAGATAC CTCAGCATTC AGGGACAGTA 540 AACATCTTAG AACTTGCCTT AGCTGTGGTC TTGCCTCTCA TTAGATACAC AAAGAAAAGC 600 CTTGTTTATT TTGGAGAAGG AATTGTTTTG TTATTTTAAG CCTTAGGGCC TTGTGGTTAG 660 AGCTACCAAT AGTAGATTGG CTTCATTATG GTTTTGAAAA TGATCACTTT CACAAGTAAG 720 AACAGGCTGT CTTAGTGGAG AATATTAGAA CAGAGACTCA AACTTAACTG AAAGTTGTTT 780 TCTGTCACTG TGCCGCTTAG GGAATTCTCA GTGCGGTGAT AAATATTCAT GGACTTCCCA 840 AGTGTTGTGT GTGCCTGGAG GCCAGTTTTT CACTTGTTCC AATTAACGGC AGGCTGCCTC 900 CACACAGGAA GTGAAACCAG CCTTTAAGCC TTTTTACAAT TCTGGCACAT GATTTGAAGA 960 TTTGGTGATG AAAGCAATGT TCTTTGAAAG TTTTGGAGCA AATAAAAAAA AGAAGCTTTT 1020 TAGATTCACT CTTAGTTTAA AAAATAACCA CTTGGGGAGT TGAAAGATGT AAGTTCTCAT 1080 CCTAGCTTTG AGAGGAACCT GCAGGGACAG CTGGGGTATA GTGTGTCCTC CTTCTAAAAC 1140 TCCACATCCT CACTTGTCAA ATGGGAAAGC AGATGGATGA TTCTAGGCCC CTTTGGGGCA 1200 GAACACTGAT TCCATCTAAA GGGGAGAGGT GGGAAGGGAT ACTTTCTCCC ATGCCGTTTG 1260 GGACACAGAG CCTCAGCCTG AGTTTGACCC TCAGCCCTGT GCGTGACTCT CGGTGTGAAC 1320 TTTCTTAGAC ATCAGCCCAG AAACGGAGAT GGAGGCTGTG TGAAGAGTTT CATTAAAAAT 1380 GAGTGATGCA GCCAGGTGCG GTGGCTCACG CCTGTAATCC CAGCACTTTG GGAGGTCAGG 1440 GTGGGTGGAT 1450
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