Tag | Content |
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EnhancerAtlas ID | HS098-51564 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr7:30130600-30132070 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NFAT5 | MA0606.1 | chr7:30131273-30131283 | AATGGAAAAT | - | 6.02 | NFATC1 | MA0624.1 | chr7:30131273-30131283 | AATGGAAAAT | - | 6.02 | NFATC3 | MA0625.1 | chr7:30131273-30131283 | AATGGAAAAT | - | 6.02 |
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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 |
GH07I030090 | chr7 | 30130479 | 30132000 |
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Enhancer Sequence | ACCCCTTCTC TACAAAAAAA TCTTTAAAAA TTAGCCAGGC GTGATGGTGC ATGCCTGTAG 60 TTCCAACTAC TCAGGAGAGT GAGGTGGGAA GATCGCTTGA GCCCAGGAGT TCAAGGCTGC 120 AGGCCACTGC CCTCCAGTCC GGGCAATACA GCAAGACCCT ATCTCTAAAT ATATATTTCC 180 TCTATCTCTC TATCTCTGTA GAGACAAATC AAGAATTATA TTCACCTAAA GTGGATTACG 240 ATTATTTTTA GGTGGGTATT GATTTTGTTT TACTCTTTTT TTTTTTTGTA CTTTACTATA 300 TTGCTTGACT TTTGTTTGAT GCCTATGATA TCTTTTTATT TTTTAATGGA GGATGGGAGG 360 TGTTTTTCTA AAAACAAGGT TAAAAATCAT TGTAGAGTGT GGTGGACCCC CGGCAGGTGC 420 TGCTCCTTAT AATGACATTT GCTTCATAAC TCCTATCAAG GTTCTTTAAA ATTTCTAGCT 480 TTATCTCACT ACATTTTTTT TTCGCTGCTA ATTTTTCTCA TAAGCTGCTA TTCCTTTACC 540 CACACGAAGC TATTGCTCAT CCAAACATTC CATTTTATAC AACTCATTAA GGATTGGGAC 600 ATTCTTTTGG GGCTAAAGGG AAAGACTGAA TGCCAGTATG ATACCTAGGG ACTTGCCCAG 660 TACATCTGAA ATAAATGGAA AATTAGGGAA AAAAAGCCAT TTGGAGTGGT TGACAGTCAT 720 CTTACAAGAA GCCAGAAAGA CTCTTAGCAA CATGGGGATT TTGCACATGA ATTGGCTGCA 780 GTTCACCGAA GGAGCTGAAA GATTTCTTTC TTTGTGCTTC TGTGAGTTTG GAAATGAAAT 840 GTCAATCCTT TCTCTGCCCA AGTGAAATTG CTGGGCCATA GAGCATTAGT TCAGCATTAG 900 CTTATGCTGA TCAAACCCAG CCATCCAGAG ATGGCAGATG AGAGAATGGA GCAGTAAACT 960 TTATTCCACA CACGTTTGTT TTAAGGACCA TTCAGCCTTA TGTTCATAGA AGCCCGTGGA 1020 AGCCCTGTAT TCTCTTGTGG CATGTATGTG AGCAACTAAG GACCCTGTCT CTGTGTGTTA 1080 CACAAGACTT TTATAAAATC CCAAATCCTC AACTTGATTT GTATGAAAAG ATGATCACAG 1140 GATTGTGGAG CTGGAAGACT CCTTCGTTCA TAGTGGGAGT CATAGTAACT ATTGCAAAAG 1200 ATTGTTATAA GGATCAAGTC GGGAATTGTG CACAGTGTCT AGCACCAGGC AAGAGCTACA 1260 AAAACGGTGG TGGTAATAAT AGTCGTTGTT ATTGTTTGAA AGGGAAGTAT GGCTCCATCC 1320 TGCCTGGAGT TTACCTGGTG GAATAAGCCT TTTCTTATTT GTTCCACTTG TCCCTGCCCT 1380 CACAGAAGAT TCACTGCTGC CCCTAGTCTC CCCACTTTGC ACTGTGTGTC ACGGCACCTT 1440 CAAGTAGAAG ACCCTCATCT AGTCATGTCT 1470
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