Tag | Content |
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EnhancerAtlas ID | HS053-02284 |
Organism | Homo sapiens |
Tissue/cell | Foreskin_keratinocyte |
Coordinate | chr1:114083760-114085620 |
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 | CTGGGCATGT GTAAGGAAAC CAGCAGGCTT GACCTTCAAA TGCCAGTGAT ATGTAGGACC 60 CAGGGCAACA GATGAAATCT GACCAATACA TTTGTGATGG CCCCTTCCAG GAACCTATGG 120 AAAGTGGACA CTCCCATTTT AATGTTTACT ATTGCCATAA TTCGTAATAT AGACGAAGAA 180 TGTGACCTTT GTTAGCAGGA GCCTTTCTTG TGACTGCTGA GGTGGTGGCT CTATTATGTA 240 GAATATAATA ACATTGCTTC ATTGCTTTAG TCTGTTTCTT CAAACTGTAA CTTGAAAAAC 300 TGACTAGTTT TAAAAATGGA AATGGCTCAA GAGACTCCAG AGTATTTAAT GCTTTTCACA 360 CTTGGGACTG GAGAGGAATT TAATTATATA AATTATTTTA AAAATCCATT AAGTTCCTGC 420 TTGCCTGTAA CGAGCGTGGC ATACTTAGAG AAATGTGTAG ATATAAACCT TCTGAGTTTA 480 AAACCTTGGA TATATTCTTT TAAGTAGGAG ACAGACTAGA AATAATGAGA AAGCATTTGA 540 ACACAGATGT GGAATATAGA GGTGACCAGA AAGAATATGT TGATAGTTGT TAGCTTATGG 600 GAATTGCAAA GGGTTTTAGT GTCAGACCTG AGTTAGTGGA TGTTCTTTTA AATTATTGTT 660 ACAAGGTTCT GCGTAACCTA CTGGTCTATG GAACTCTTAT CTCAGATTGT GTGGACTCTT 720 CCTCACTTTC TAAGAGCCAG CAACACTGGA TTTCTCTCAG TTCCTCTAAC CACTGTGTTC 780 TTCCCCAGCT CAAGTAAGTG CTGTCGCATG TCTTGTTTCC TCTACCAACA TTTCCCCCAC 840 TGCCCTTTTT GCCTTGCTGG CTCCTATTTA TCTTTCAGAT TTCAGCTACA ATGGCACTTA 900 GTGAAGTCTT CCCATAACTC CCAGATTTAG GATCTAAGTT GTAAATTCCC ACAATACTCT 960 GTACAGTAGT CCCCCCCTCC TTATTCTTGG GGGATATGTC CCAAGACCCC CCAGTGGATG 1020 CCGGAAACCA TGGATTGTAC CAGATCCTAC ATATACTATG TTTTTTGATC TAATAACCCA 1080 GACAGCTACT AAGATAGCTA CTGAGTAACT AATGTGTGGG TAGCATGTAT GGCATGGATA 1140 TAGAGATGAT ACAGCAGGAC AAAGGGATGA CTCACATCCC AGGCGGGATG GAACAGGACG 1200 GTATGGGAGT TGAGTTCATT GCAGCACTCA GAATGGCATG CAATCTAAAA CTCATTAATT 1260 GTTTATGTCT GGAACTTTCC ATTTAATACT TTCAGACCAA GGCTGACTGT GGGTAACTGA 1320 AACCGTGGAA GACAAAACGT TAGATAAAGA GGAACTCCTG TACTTCTCTT TTATAATGTT 1380 TCCACGTTTG AAATTTCTTC TTCAATGTTT ATCTTCCCTG CAAGACTTTA AGTTCCCTTT 1440 GGGCTCACTC TCATTCACTG CGTTTAGCCC TAAGTACCTA CTCCTCAGAA CTCAGAAATG 1500 ACTAGACTGT GTCATGGAAA AGTAGGCTGT TATGAAACAG GAAACCTGTA CTCTATAAGC 1560 TTATGCAAAA GAAGAAATTC ATCAAAAGGG ACCATGTCTC TTACACACAC AGGTACATAC 1620 GCGTGTGCAC ACACACAAAC ACACAGAGAA AGAGAGAGGG AGAGAGAGAA AGAAACAGGG 1680 ATATTCTAGG ACAGCGCTTA CAATGTTTAC AGTGTAGGCT CTGAAGACAG ATTGACTGTG 1740 TTCACATCCC AGGTCTGTCA CTTACTAGCA GTGTAACCTT GGCCAAGTTA CTTGACTTCT 1800 CAATACTTTA GCTTCTTACC TATAAAATGG GAATAATAAT AACACCTACT TCAAAGGTTA 1860
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