Tag | Content |
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EnhancerAtlas ID | HS176-02023 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr1:114084440-114085550 |
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 | CTGGTCTATG GAACTCTTAT CTCAGATTGT GTGGACTCTT CCTCACTTTC TAAGAGCCAG 60 CAACACTGGA TTTCTCTCAG TTCCTCTAAC CACTGTGTTC TTCCCCAGCT CAAGTAAGTG 120 CTGTCGCATG TCTTGTTTCC TCTACCAACA TTTCCCCCAC TGCCCTTTTT GCCTTGCTGG 180 CTCCTATTTA TCTTTCAGAT TTCAGCTACA ATGGCACTTA GTGAAGTCTT CCCATAACTC 240 CCAGATTTAG GATCTAAGTT GTAAATTCCC ACAATACTCT GTACAGTAGT CCCCCCCTCC 300 TTATTCTTGG GGGATATGTC CCAAGACCCC CCAGTGGATG CCGGAAACCA TGGATTGTAC 360 CAGATCCTAC ATATACTATG TTTTTTGATC TAATAACCCA GACAGCTACT AAGATAGCTA 420 CTGAGTAACT AATGTGTGGG TAGCATGTAT GGCATGGATA TAGAGATGAT ACAGCAGGAC 480 AAAGGGATGA CTCACATCCC AGGCGGGATG GAACAGGACG GTATGGGAGT TGAGTTCATT 540 GCAGCACTCA GAATGGCATG CAATCTAAAA CTCATTAATT GTTTATGTCT GGAACTTTCC 600 ATTTAATACT TTCAGACCAA GGCTGACTGT GGGTAACTGA AACCGTGGAA GACAAAACGT 660 TAGATAAAGA GGAACTCCTG TACTTCTCTT TTATAATGTT TCCACGTTTG AAATTTCTTC 720 TTCAATGTTT ATCTTCCCTG CAAGACTTTA AGTTCCCTTT GGGCTCACTC TCATTCACTG 780 CGTTTAGCCC TAAGTACCTA CTCCTCAGAA CTCAGAAATG ACTAGACTGT GTCATGGAAA 840 AGTAGGCTGT TATGAAACAG GAAACCTGTA CTCTATAAGC TTATGCAAAA GAAGAAATTC 900 ATCAAAAGGG ACCATGTCTC TTACACACAC AGGTACATAC GCGTGTGCAC ACACACAAAC 960 ACACAGAGAA AGAGAGAGGG AGAGAGAGAA AGAAACAGGG ATATTCTAGG ACAGCGCTTA 1020 CAATGTTTAC AGTGTAGGCT CTGAAGACAG ATTGACTGTG TTCACATCCC AGGTCTGTCA 1080 CTTACTAGCA GTGTAACCTT GGCCAAGTTA 1110
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