Tag | Content |
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EnhancerAtlas ID | HS052-02212 |
Organism | Homo sapiens |
Tissue/cell | Fibroblast_foreskin |
Coordinate | chr1:114084250-114085580 |
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 | TATATTCTTT TAAGTAGGAG ACAGACTAGA AATAATGAGA AAGCATTTGA ACACAGATGT 60 GGAATATAGA GGTGACCAGA AAGAATATGT TGATAGTTGT TAGCTTATGG GAATTGCAAA 120 GGGTTTTAGT GTCAGACCTG AGTTAGTGGA TGTTCTTTTA AATTATTGTT ACAAGGTTCT 180 GCGTAACCTA CTGGTCTATG GAACTCTTAT CTCAGATTGT GTGGACTCTT CCTCACTTTC 240 TAAGAGCCAG CAACACTGGA TTTCTCTCAG TTCCTCTAAC CACTGTGTTC TTCCCCAGCT 300 CAAGTAAGTG CTGTCGCATG TCTTGTTTCC TCTACCAACA TTTCCCCCAC TGCCCTTTTT 360 GCCTTGCTGG CTCCTATTTA TCTTTCAGAT TTCAGCTACA ATGGCACTTA GTGAAGTCTT 420 CCCATAACTC CCAGATTTAG GATCTAAGTT GTAAATTCCC ACAATACTCT GTACAGTAGT 480 CCCCCCCTCC TTATTCTTGG GGGATATGTC CCAAGACCCC CCAGTGGATG CCGGAAACCA 540 TGGATTGTAC CAGATCCTAC ATATACTATG TTTTTTGATC TAATAACCCA GACAGCTACT 600 AAGATAGCTA CTGAGTAACT AATGTGTGGG TAGCATGTAT GGCATGGATA TAGAGATGAT 660 ACAGCAGGAC AAAGGGATGA CTCACATCCC AGGCGGGATG GAACAGGACG GTATGGGAGT 720 TGAGTTCATT GCAGCACTCA GAATGGCATG CAATCTAAAA CTCATTAATT GTTTATGTCT 780 GGAACTTTCC ATTTAATACT TTCAGACCAA GGCTGACTGT GGGTAACTGA AACCGTGGAA 840 GACAAAACGT TAGATAAAGA GGAACTCCTG TACTTCTCTT TTATAATGTT TCCACGTTTG 900 AAATTTCTTC TTCAATGTTT ATCTTCCCTG CAAGACTTTA AGTTCCCTTT GGGCTCACTC 960 TCATTCACTG CGTTTAGCCC TAAGTACCTA CTCCTCAGAA CTCAGAAATG ACTAGACTGT 1020 GTCATGGAAA AGTAGGCTGT TATGAAACAG GAAACCTGTA CTCTATAAGC TTATGCAAAA 1080 GAAGAAATTC ATCAAAAGGG ACCATGTCTC TTACACACAC AGGTACATAC GCGTGTGCAC 1140 ACACACAAAC ACACAGAGAA AGAGAGAGGG AGAGAGAGAA AGAAACAGGG ATATTCTAGG 1200 ACAGCGCTTA CAATGTTTAC AGTGTAGGCT CTGAAGACAG ATTGACTGTG TTCACATCCC 1260 AGGTCTGTCA CTTACTAGCA GTGTAACCTT GGCCAAGTTA CTTGACTTCT CAATACTTTA 1320 GCTTCTTACC 1330
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