Tag | Content |
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EnhancerAtlas ID | HS105-08206 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr10:1155780-1156950 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
JUN(var.2) | MA0489.1 | chr10:1156298-1156312 | AGGAAATGAGTCAT | + | 7.28 |
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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 |
GH10I001109 | chr10 | 1155641 | 1157181 |
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Enhancer Sequence | ACTAATGTGG ACCTATGAAT ACAGTTTCCT AGGGTTTATG TCTTCCTATT GGAATCAGGT 60 GTGGGGGTAG AGTAAGGTGG AGTGTGTAAT TCCCGTGTGC CCTTTCTCCC ACATGGGTCT 120 TCCAGGCTGT AGGCTGTGCT TCCATTCACC TGAACCACGG GGGTGAGGTG AACGTGGACC 180 AGACCTGCCC GGGCCATGCT TACTCAGATC GTTTACGCTT TCTTTTTTCT TACTCAAATT 240 ATCATGAACT AGCGTATCTT GTTGATGTGT ACATCCAAAA ATACGTTTTG AAAAGATCTC 300 TCTTTGGCGC TAATTTTGTT GCTGTGTCGG GGCGAGTCCG CTGGGCTGTT GGACATTGAG 360 CTTCCCCTCA CCGGCCTGGC GGTTTCTCAG CTGTGCGCAT GCAGGATGAG GGCTTGGTCA 420 GCAGGTGGAG CCGTGGACGC CTTTATTGAA CACAAACTCT TCCTTCCTGA CATCAGATCA 480 GCTGTAAACC TTTAGACGTG CCTCATAATG AGAAAAGCAG GAAATGAGTC ATTTTACAAA 540 AATGTTTCAT CTGAGGTGTC TTCTTAGTAA CACTTGCCTT TGTCTCCGGC ATGGGTTTTG 600 TAGGTTCGAG CCAATACGAC AAATAAAACC TACAGAGTGC GTGATCCTTA CAAATGTGTA 660 GAGCTGTGCA TCCGCGCCAC AGCACACCAG GGTGAGGGCC TCGCAGTGCG GTTTAGGTCC 720 TGAGATGTGC GTCCGCGCCC CAGCACACCT GGGTGAGGTC CGGGGTGCGG GTTTAGTTCC 780 TGAGAGGAAT GGCCAGGTTG TGTGTGTGTG TTCCGTTTGG TCACTTGTCT GGGACGTTCT 840 GAACATGACT TGTAAGAGCA CACCCTGGGT CCCCTGCCTT CCCTGCCACC ATGTCATTCT 900 GAGGGACCCT CTGCGCCGGG GGCTTCTCTG CAGTGGCCAC GGCATCGCCA AGGACATCCG 960 TGAGCCTCCG ATGGGTGTCC AGCGTGTTAG CGCCCAGACC CACAGGGCCT GGCACCCTGA 1020 TAGGTGGGAA TGTTGGCCCA GGGCCGGGCC TGAGGCCTGC AGGACTGCCT GCTCATCCGG 1080 GAAGTAGCTC TGCCGGTTTT ACAGGGTGAT CCTGAGTTCT TTTCACTAGT TCTTTTCCTG 1140 AGCATTGAAA GCAAAAGTCA GACATGTGTT 1170
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