Tag | Content |
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EnhancerAtlas ID | HS176-35412 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr6:125518780-125519940 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Myod1 | MA0499.1 | chr6:125519853-125519866 | TGCAGCTGTCTCT | + | 6.36 | Nr5a2 | MA0505.1 | chr6:125519058-125519073 | CAGCTCAAGGTCAGT | + | 6.34 |
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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 |
GH06I125196 | chr6 | 125517431 | 125520292 |
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Enhancer Sequence | TTTTCACCCA AGGTGGAATA TAATATAAAG TACTAATCAG TTATACAAAC ATGTTATTTA 60 TAAAATAACA GCCCACTAAG CGTCAGAGGT GAGGGGTTGC CCCATCCAAT TTTCAGAGTC 120 TAAAAGAGGC ATCTGGGTGT CCATTACCTG AAACAGCACA GGCGCTAGTG TCTCCAGAGA 180 AAAGGAAATG GAAGAGGGAG GCAGGGGATG TTACAACAGG GTGTGATTAA TAGCAGCTCA 240 CTGCTGGAGT TCACTCAGGA AAGGCTGGGT AAATGCTGCA GCTCAAGGTC AGTGTGAGGC 300 AGGCCAAGGG ATCGGTTAGC CCTGGAACTT CTGAGTGAGT CCTTGGCTCC AGTTAAATAA 360 GAAGCAGCCA AGATCTGGGA AGGTCAACAC AGTCAAAGCC CTACCAGGAA CTAGGATTAT 420 ACCCTGGGCT TCAAGCCAAG ACCAGGGCAC TCTGGCTGAT CTGAGTGTGA TCTTGAACTC 480 TGCTTTGCCC TCTGAGAGAA GGAGCCGAAG CTCTGTCTAC CTTCAGGGAC AGAGGTCTGG 540 AGTTAGTTTC CTGATTACAG CAGGAACAAC CCAAGAGGCC ATCAGATACT GGGAGGTTCT 600 TACAGTGCTC TAAACCCTTT CAGGCAATTT GAGTCTTCTG TGTCTATTGT CTTCACAGGC 660 ATCTTGTATA GTGTTGGAAA CCTATAGTGA TAAGTGATTT TCAGCTACTT ACTAGAGATG 720 GGAGAATTTC AAAGTCCTTT CCTTCATTGT CCATCTTTAC TCATTTGGGT AGAGTTATAC 780 CCAGTTCTAT CCCTGCATAC ATACTTGCAT GCATGGGGTA AGAGAGATCT ATTTACAAAC 840 ACGTGACCAC AAACACATGA CCAGCTTCCA AAGCTGAGAA TGCCAAGGAC ACATGGAAGT 900 TATTGGTCAC CTGAGTATAG AAAAAGCAGG GAAACCCAGC TCAACCACTT TCTGTCTATG 960 AACGTCAATT TTCCTCTTTA TAAATTAGGG ATGTGTATAA AATAATGTGC ATAAAATCTT 1020 TGGCACAGTG CCTAACACAT TGTGAACACA AGTGTCAGCC AAAATTATGA GCATGCAGCT 1080 GTCTCTGTGT CTGTTGAGCA GAGCTTCCTC AATGTGTTGT CAATGGCTCA ATTTTGGAAA 1140 CGGGCAATGT CTCGAGACAG 1160
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