Tag | Content |
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EnhancerAtlas ID | HS105-04413 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr1:114084370-114085490 |
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 | GGGTTTTAGT GTCAGACCTG AGTTAGTGGA TGTTCTTTTA AATTATTGTT ACAAGGTTCT 60 GCGTAACCTA CTGGTCTATG GAACTCTTAT CTCAGATTGT GTGGACTCTT CCTCACTTTC 120 TAAGAGCCAG CAACACTGGA TTTCTCTCAG TTCCTCTAAC CACTGTGTTC TTCCCCAGCT 180 CAAGTAAGTG CTGTCGCATG TCTTGTTTCC TCTACCAACA TTTCCCCCAC TGCCCTTTTT 240 GCCTTGCTGG CTCCTATTTA TCTTTCAGAT TTCAGCTACA ATGGCACTTA GTGAAGTCTT 300 CCCATAACTC CCAGATTTAG GATCTAAGTT GTAAATTCCC ACAATACTCT GTACAGTAGT 360 CCCCCCCTCC TTATTCTTGG GGGATATGTC CCAAGACCCC CCAGTGGATG CCGGAAACCA 420 TGGATTGTAC CAGATCCTAC ATATACTATG TTTTTTGATC TAATAACCCA GACAGCTACT 480 AAGATAGCTA CTGAGTAACT AATGTGTGGG TAGCATGTAT GGCATGGATA TAGAGATGAT 540 ACAGCAGGAC AAAGGGATGA CTCACATCCC AGGCGGGATG GAACAGGACG GTATGGGAGT 600 TGAGTTCATT GCAGCACTCA GAATGGCATG CAATCTAAAA CTCATTAATT GTTTATGTCT 660 GGAACTTTCC ATTTAATACT TTCAGACCAA GGCTGACTGT GGGTAACTGA AACCGTGGAA 720 GACAAAACGT TAGATAAAGA GGAACTCCTG TACTTCTCTT TTATAATGTT TCCACGTTTG 780 AAATTTCTTC TTCAATGTTT ATCTTCCCTG CAAGACTTTA AGTTCCCTTT GGGCTCACTC 840 TCATTCACTG CGTTTAGCCC TAAGTACCTA CTCCTCAGAA CTCAGAAATG ACTAGACTGT 900 GTCATGGAAA AGTAGGCTGT TATGAAACAG GAAACCTGTA CTCTATAAGC TTATGCAAAA 960 GAAGAAATTC ATCAAAAGGG ACCATGTCTC TTACACACAC AGGTACATAC GCGTGTGCAC 1020 ACACACAAAC ACACAGAGAA AGAGAGAGGG AGAGAGAGAA AGAAACAGGG ATATTCTAGG 1080 ACAGCGCTTA CAATGTTTAC AGTGTAGGCT CTGAAGACAG 1120
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