Tag | Content |
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EnhancerAtlas ID | HS074-13681 |
Organism | Homo sapiens |
Tissue/cell | GM19239 |
Coordinate | chr6:126035440-126036400 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF1 | MA0050.2 | chr6:126035721-126035742 | TTCCATTTTCAGTTTTCATTT | + | 6.02 | IRF1 | MA0050.2 | chr6:126035709-126035730 | TTGTCCTTTCACTTCCATTTT | + | 6.59 | IRF1 | MA0050.2 | chr6:126035715-126035736 | TTTCACTTCCATTTTCAGTTT | + | 7.13 | NFAT5 | MA0606.1 | chr6:126035680-126035690 | AATGGAAAAT | - | 6.02 | NFATC1 | MA0624.1 | chr6:126035680-126035690 | AATGGAAAAT | - | 6.02 | NFATC3 | MA0625.1 | chr6:126035680-126035690 | AATGGAAAAT | - | 6.02 | RFX5 | MA0510.2 | chr6:126035825-126035841 | GGTTGCCATGGCAGCT | + | 6.22 | RFX5 | MA0510.2 | chr6:126035825-126035841 | GGTTGCCATGGCAGCT | - | 6.32 | SOX10 | MA0442.2 | chr6:126035497-126035508 | AAAACAAAGAC | + | 6.14 |
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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 | TATGTTCTGC TTAGTAAACA TAACAAAACA TTTGGGAAAA ATAAAAGGAA GCATAATAAA 60 ACAAAGACAT TGAGGTGGAA GCTGTGAACA GTAAAGACCG TACCAAAAAA AGAAGATTCA 120 CAAAACATGC TTCCTTCCAA ACATTAGGCT CATCAGACAG TTGCATGAAA GGAAAGGCCC 180 TGATTTTTAT GACAAGCAAG TAGAAGCAAA CCCACAGAAC AATCTATCCA TTTGGGTATA 240 AATGGAAAAT CTAGTGCCCT CCTGCCTTCT TGTCCTTTCA CTTCCATTTT CAGTTTTCAT 300 TTTCACACCC CACAGAAGCT GATGCTGTGC CCTATGCACT GACTCCTATC CCACAACAAA 360 AAGACTTCCC CAACTGAATA GGCATGGTTG CCATGGCAGC TAGGGGGTCA TAAACTCCTG 420 AGCTGTGGGT CCTGGCACAA TTCCACGCAT TATCTGCATC CTGGTGCAAA TCAGTCCCTT 480 TATCTAATTA GTAGCCTTAC AAATAGCCAC CTGCCCCAAA GCTTAACCAT TAAAGATGCA 540 ATATTGGCTG AATAGCTTGA GACCAGAGGT GAGGATATCA GAAAACTGAA AGCTGATCTG 600 AGTGAGGCCC TATCTCTCCT GGCTACTGAC ACCTGTGAGC CCTAGCCCAC CCACATACCA 660 GGAGTTCAGA AGGAGACCAA GAACAAATCA CTTCTGTCTT CTTTTCGTGA CTCACCTTGG 720 GTGTCTTCTG ATGCACTGGC CTCCCAGAAG CTGGGCCTGC TGACCTCTGT CTAAAGGACC 780 TGGTTCATCA TTCCTGCTTA GATGCCCAAC CCTTCCCTGC CTGAGAACTT CCTCCCTAAG 840 AAGTCCAGCC CTGTCTCTCT CTCTCTAGAA CTTCATCAAC TGCCCTGGCC TGTTGTAGTT 900 CACTACCTGA TCTGGATCCT TCAGAACTAT CTCTTGATTT ACTCCAAAGA CTGACTCCTC 960
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