Tag | Content |
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EnhancerAtlas ID | HS095-07701 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr12:102287990-102289320 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOSL1 | MA0477.1 | chr12:102288700-102288711 | GATGAGTCACC | - | 6.32 | JUND | MA0491.1 | chr12:102288700-102288711 | GATGAGTCACC | - | 6.62 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr12 | 102288337 | 102288971 | chr12 | 102289190 | 102289276 |
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| Number: 1 | ID | Chromosome | Start | End |
GH12I101894 | chr12 | 102288127 | 102289389 |
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Enhancer Sequence | GTTCAAATGA TTCTCCTGCC TCAGCCTCCT GAGTAGCTGG GATTACAGGC ATGCACCACT 60 ATGCCTGGCT AATTTTTATA TTTTAGTAGA GATGGGGTTT CACCATGTTG GCCAGGCTGG 120 TCTTGAACTC CTAACCCGAA GTGATCCACC CGTCTCAGCC TCCCAAAGTG CTGGGATTAC 180 AGGCATGAGC TACCACACCC GGCCAATTTT TGTATTTTTT GTAGAGACAG GGTTTCACCA 240 TGTTGCCCAG ACTGGTTTCG AACTCCTGAG CTCAAGTGAT CCATCCTCCT CGGCCTCCCA 300 AAATGCTGGG ATTACAGGTG TGAGCTACCG TGCCTGGCCT CCACCTGTAT GGTTTTAAAT 360 GTACAGATAA GCAAGAATAG AACACGACCC TGGAATTCCA AGTTTTCAGA TCACGTGTTT 420 GATGTCATGT GGACTCCACA CCTGGGCCTT TGACATAGTC TCAATTTGCC ATCAATAGAC 480 AGAGTCCCCA GGTCTGGTCT TCTCTTCAGT CAGAGCACCT AGAGCACCTT CATATCGCCA 540 CCTCCCTATC TTCCTAAATA TCCTCCTCAT TCTTTCATTG CCTTCCCTTT CTCCACAGAC 600 AGGCAAACAA CCTTCTTCCC AGCGCTTCTC CTCTGTGTTT GCTCCGATGC CTGGCATGTG 660 GCTGTCTGAG GTTCAGAATT ATTCTCAGAC CTGTGTAACA AGAACTCTAG GATGAGTCAC 720 CTGGTGCCTG CTTTTTTATA CCCTCAGGCC AAGGCAGGGA GGCCTGATTT CCCTGGCAGA 780 GTTAATTGTG TGGCAAAAGT GCTGCCCAAG GTTATGAGCT GTCTCTGCTT TTTTCCCCAT 840 TACTGGTTCC CATTCCTGTC TCTCTGCCCA TTCAGCATTG TGCTCAGAAG GGCATCCTCC 900 ACCTCAACAT TCCTGTAGTG TGAAAAATGG TTATTGTAGG AAAAGTGGTA ATGCTAAATT 960 CGAAACCCTT CAGGTTTTTT TTTTTTTTTT TTTTTTTTTT TTTTACCCAG GCTGGAGTGC 1020 AGTGGCGTGA TCTCAGCTCA CTGCAAACTC TACCTCCTGG GTTCAAGTGA TTCTCCTGCC 1080 TCAGTCTCCC GAGTAGCTTG GATTACAGGC ACGCTGTACC ATGCCCAGTT AATTTTTGTA 1140 TTTTTAGTAG AAACAGGGTT TCACCATGTT GGCCAGGCTG GTCTCGAACT CCTGAGCTCA 1200 AGTGATCTTC CCGCCTCGGC CCACAGAAGT CCTGGAATTA CAGGCATGAG CCACTATACC 1260 CAGCCTAAAT CCTAAACCCT TCAGGTTCTT GCAATACCAG TGACATTGAA ATTGAATTAA 1320 TTTGGAATAA 1330
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