Tag | Content |
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EnhancerAtlas ID | HS139-02855 |
Organism | Homo sapiens |
Tissue/cell | Myotube |
Coordinate | chr1:114084530-114085500 |
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 | chr1:114084921-114084935 | AAGGGATGACTCAC | + | 6.29 |
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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 |
GH01I113541 | chr1 | 114084197 | 114085863 |
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Enhancer Sequence | CACTGTGTTC TTCCCCAGCT CAAGTAAGTG CTGTCGCATG TCTTGTTTCC TCTACCAACA 60 TTTCCCCCAC TGCCCTTTTT GCCTTGCTGG CTCCTATTTA TCTTTCAGAT TTCAGCTACA 120 ATGGCACTTA GTGAAGTCTT CCCATAACTC CCAGATTTAG GATCTAAGTT GTAAATTCCC 180 ACAATACTCT GTACAGTAGT CCCCCCCTCC TTATTCTTGG GGGATATGTC CCAAGACCCC 240 CCAGTGGATG CCGGAAACCA TGGATTGTAC CAGATCCTAC ATATACTATG TTTTTTGATC 300 TAATAACCCA GACAGCTACT AAGATAGCTA CTGAGTAACT AATGTGTGGG TAGCATGTAT 360 GGCATGGATA TAGAGATGAT ACAGCAGGAC AAAGGGATGA CTCACATCCC AGGCGGGATG 420 GAACAGGACG GTATGGGAGT TGAGTTCATT GCAGCACTCA GAATGGCATG CAATCTAAAA 480 CTCATTAATT GTTTATGTCT GGAACTTTCC ATTTAATACT TTCAGACCAA GGCTGACTGT 540 GGGTAACTGA AACCGTGGAA GACAAAACGT TAGATAAAGA GGAACTCCTG TACTTCTCTT 600 TTATAATGTT TCCACGTTTG AAATTTCTTC TTCAATGTTT ATCTTCCCTG CAAGACTTTA 660 AGTTCCCTTT GGGCTCACTC TCATTCACTG CGTTTAGCCC TAAGTACCTA CTCCTCAGAA 720 CTCAGAAATG ACTAGACTGT GTCATGGAAA AGTAGGCTGT TATGAAACAG GAAACCTGTA 780 CTCTATAAGC TTATGCAAAA GAAGAAATTC ATCAAAAGGG ACCATGTCTC TTACACACAC 840 AGGTACATAC GCGTGTGCAC ACACACAAAC ACACAGAGAA AGAGAGAGGG AGAGAGAGAA 900 AGAAACAGGG ATATTCTAGG ACAGCGCTTA CAATGTTTAC AGTGTAGGCT CTGAAGACAG 960 ATTGACTGTG 970
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