Tag | Content |
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EnhancerAtlas ID | HS098-56029 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr8:123771610-123773040 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
GSC | MA0648.1 | chr8:123772207-123772217 | GCTAATCCCC | + | 6.02 | MAFF | MA0495.3 | chr8:123772745-123772760 | GTGCTGAGTCAGCTC | - | 6.55 | MAFF | MA0495.3 | chr8:123772745-123772760 | GTGCTGAGTCAGCTC | + | 6.63 | Nr2f6(var.2) | MA0728.1 | chr8:123772643-123772658 | AGGGTCAAGGGGTCA | + | 6.3 | Sox6 | MA0515.1 | chr8:123771977-123771987 | AAAACAATGG | - | 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: 2 | ID | Chromosome | Start | End |
GH08I122757 | chr8 | 123770125 | 123771616 | GH08I122759 | chr8 | 123771833 | 123773263 |
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Enhancer Sequence | AGAGAAAAAG TAGCTGAGTA AGTATTCTCA TTCAGGACTG CTTAACTCCA AAGCCCTGCT 60 CCTAACAGTG AAGCCACAGA GATTCTCCTA AGGAGTAATA AGAACGTCCC AGAAGCAGCT 120 CAGTTCAGTA GATATTTATC GATCATATAC GACATGCCCC ATACCATATT AAGCCTTAGA 180 GATTAAATAA GACAGAAATG GTCCTTGACA AATAGAGTTC AGTGAAGACA ACTATGGAAT 240 TTACTCATCC AACAAATACT TATTGAGCAT CTACTATATG CCAGAGCCAG ACACAATTCT 300 AAATGTTAGA AGATGCGACA GGGAACAAAA AAGGCAGGGA TGCTGCCTTC ATAGGTTAGG 360 ACATTTCAAA ACAATGGAAT TGAGCATTTT CGACAGGTAG TGAATGAGTT GAAAAAAGAA 420 ACAAGAGCCC TACACTCAGC CCCAGCTGGG ATGTGCTAAC TGCCTTTCCA GCCCTCCGGG 480 GAGCCATCTC CCAGCTGAAA ACCTGGCCTG CCGAGGAGTA GTCACCCACC CTGGCAGCTC 540 CTGAGTTCCA TCCTGGGAGG GGATTGAGAG GGGCTGACTG GAGTATGGTG CTATGTAGCT 600 AATCCCCAGT TGCGCTGGGT CCTCAGAAAC TCTCCAATTA ACACACGGGG CCATGAAGTT 660 CTTCTCCTCA CAAGTGCTCC CAAGGAGATG AATTTTAATT CACTTTCCTT TCAAGAGTAA 720 CTGTGTTGGC AAGCAACATT TTGTCACGGG AGGATGAGCA GAAGGTGTGT TAAAGGCAAC 780 AGGATGATGT TAAATGTTTG CTCCACAATG TTTAGGAATA AGGGAAGCTT TTTTTAAATT 840 AAGTGCCTTA GAACTGGAGG GAGGGAGGAG GGGCATGGTT GGAAGTTTTC ACATGAACCA 900 ACAACAGATG TTCTGTCTAC AGTCCGGGGA GTGTGAACTA CCACGGAGGC TACGTGGAGC 960 GCGTGGCATC TGTGTTTGGA AAGCTTCATA ACCACCTGCT GTGAGCGGGA CATGCTTCCT 1020 CAGCATCTGA GTTAGGGTCA AGGGGTCAAC CTGAACTGAT AAGCCCCAGT GAACATTTCT 1080 TTCAGGCTGG GCTTGAAACC TCAGAGGGCC CCATGACTAA GCGCTGGTCC TGTGTGTGCT 1140 GAGTCAGCTC AGCCATCCTC CTGCCAAGGG GCACACGTCC CAAGGCAACA TGAAGTTTCC 1200 TCTTTCGAGT GAGTCCATTT GGATCAAAGT CTTCAGTAAA TGGAGAAACA GGAGGTACTG 1260 CCACAGCAAA CTCAAGCTGG TGCTCTGTAA ATGGTGGAAG TGTAGAAACC CCGAGCTGGT 1320 CCATCCTTGT CTTTCCTGAG TATGAGGTGG AAAAACGGAA GCCCAGGAAG TTGAAATGGA 1380 TTGCTTGAGG ACACACAGCA GGCCACATCT GCTGAATCCT TCTTGGGGCT 1430
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