Tag | Content |
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EnhancerAtlas ID | HS147-02674 |
Organism | Homo sapiens |
Tissue/cell | NHEK |
Coordinate | chr1:114084120-114085750 |
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) |
Arid3b | MA0601.1 | chr1:114085664-114085675 | ATAATTAATAT | - | 6.02 | 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 | CTTGGGACTG GAGAGGAATT TAATTATATA AATTATTTTA AAAATCCATT AAGTTCCTGC 60 TTGCCTGTAA CGAGCGTGGC ATACTTAGAG AAATGTGTAG ATATAAACCT TCTGAGTTTA 120 AAACCTTGGA TATATTCTTT TAAGTAGGAG ACAGACTAGA AATAATGAGA AAGCATTTGA 180 ACACAGATGT GGAATATAGA GGTGACCAGA AAGAATATGT TGATAGTTGT TAGCTTATGG 240 GAATTGCAAA GGGTTTTAGT GTCAGACCTG AGTTAGTGGA TGTTCTTTTA AATTATTGTT 300 ACAAGGTTCT GCGTAACCTA CTGGTCTATG GAACTCTTAT CTCAGATTGT GTGGACTCTT 360 CCTCACTTTC TAAGAGCCAG CAACACTGGA TTTCTCTCAG TTCCTCTAAC CACTGTGTTC 420 TTCCCCAGCT CAAGTAAGTG CTGTCGCATG TCTTGTTTCC TCTACCAACA TTTCCCCCAC 480 TGCCCTTTTT GCCTTGCTGG CTCCTATTTA TCTTTCAGAT TTCAGCTACA ATGGCACTTA 540 GTGAAGTCTT CCCATAACTC CCAGATTTAG GATCTAAGTT GTAAATTCCC ACAATACTCT 600 GTACAGTAGT CCCCCCCTCC TTATTCTTGG GGGATATGTC CCAAGACCCC CCAGTGGATG 660 CCGGAAACCA TGGATTGTAC CAGATCCTAC ATATACTATG TTTTTTGATC TAATAACCCA 720 GACAGCTACT AAGATAGCTA CTGAGTAACT AATGTGTGGG TAGCATGTAT GGCATGGATA 780 TAGAGATGAT ACAGCAGGAC AAAGGGATGA CTCACATCCC AGGCGGGATG GAACAGGACG 840 GTATGGGAGT TGAGTTCATT GCAGCACTCA GAATGGCATG CAATCTAAAA CTCATTAATT 900 GTTTATGTCT GGAACTTTCC ATTTAATACT TTCAGACCAA GGCTGACTGT GGGTAACTGA 960 AACCGTGGAA GACAAAACGT TAGATAAAGA GGAACTCCTG TACTTCTCTT TTATAATGTT 1020 TCCACGTTTG AAATTTCTTC TTCAATGTTT ATCTTCCCTG CAAGACTTTA AGTTCCCTTT 1080 GGGCTCACTC TCATTCACTG CGTTTAGCCC TAAGTACCTA CTCCTCAGAA CTCAGAAATG 1140 ACTAGACTGT GTCATGGAAA AGTAGGCTGT TATGAAACAG GAAACCTGTA CTCTATAAGC 1200 TTATGCAAAA GAAGAAATTC ATCAAAAGGG ACCATGTCTC TTACACACAC AGGTACATAC 1260 GCGTGTGCAC ACACACAAAC ACACAGAGAA AGAGAGAGGG AGAGAGAGAA AGAAACAGGG 1320 ATATTCTAGG ACAGCGCTTA CAATGTTTAC AGTGTAGGCT CTGAAGACAG ATTGACTGTG 1380 TTCACATCCC AGGTCTGTCA CTTACTAGCA GTGTAACCTT GGCCAAGTTA CTTGACTTCT 1440 CAATACTTTA GCTTCTTACC TATAAAATGG GAATAATAAT AACACCTACT TCAAAGGTTA 1500 TCATGAGGAG TGAGTTAAAA CATATAGCAT ATACTATAAT AAATATAATT AATATGTATA 1560 TAATAATGAT AATAATTCTA AAATAACAGC CCTAGTCATC AGTGTTTCCA TTTCTTGTTC 1620 TTGTCTCATT 1630
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