Tag | Content |
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EnhancerAtlas ID | HS136-08656 |
Organism | Homo sapiens |
Tissue/cell | Monocyte |
Coordinate | chr17:76609060-76610490 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOSL1 | MA0477.1 | chr17:76609424-76609435 | CATGAGTCACC | - | 6.62 | JUND | MA0491.1 | chr17:76609424-76609435 | CATGAGTCACC | - | 6.02 |
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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 |
GH17I078613 | chr17 | 76609543 | 76609887 |
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Enhancer Sequence | CGTGCATTAG GCCATTATCT ATTGTCCCAG AGACACACAT AATTAGGATG CTGTGGTGGC 60 TTTGAGTTTC ATGTTGCTTA AGATAGTTTT TTTTTCTTTT TTGAGACAGG GTCTCACTCT 120 GTTACCCAGG CTGGAGTGCA GTGGCATGAC CACAGCTCAC TGCAGCCTCG ACCTCCTGGG 180 CTCAAGTGAT CCTCCCACCT CAGCCTTCCC AGTAGCTGGG ACTACAGGAG CACACCACTA 240 GGCCCAGCTA ATGTTTTGTA CTATTTGTGG AGACGGGGTT TTGCCATGTT GCCCAGGCTG 300 GTCTCGAACT CCCGGACTCA AGCAATCCTC CCACCTTGGC CTCCCAAAGT GCTGGGATTA 360 CAGGCATGAG TCACCATGCC CAGCCTTAAG ATAGTTTTGA TGATTGTCAA GATTTTCAAG 420 CAAGGCTAGG CCCAAAACTA CGGAGAAACC CTCAATCCAT CTGGTCTCCA TTTGCATGTA 480 GGACTGAGAG ATCTCAGTAA CCAGCACCTT TCCTCTCCTG GATCAGGCAA AGAATCGCAC 540 GTGCCAGCCA CATCCTCCAT ATGGCTTTCT CAGGCTCTGT TCTGCAATTA GAAGATAATC 600 ACATGCAAAT ACCTCTTGCA GGGTGTCACG AGAAAGGAAA CCGTTCCTCC TCTGGAGAAC 660 GTGCCCATCT TGCGTCACAC GCAAAAAAGA TGTCTTTGAG TCTCATAACC TTTAGAGAGT 720 ACATTTCACA ATGTCACGAC GTACCCTTGC CTGATGCGTT GATATCATCT TTTCTGTGTG 780 TGTCAAGAAT CTGTACAAAG CATGAATTAT GTATTTGGTG GTTTAGGCTA AGCAGCCTCT 840 GAAAGCCAGA CCGGGTCATC GCTGGGATCT CTCCATCGTG CTCAGCAAGC TGGAGATGGA 900 ATCCCCATTG ATGAAAGTCA GATAACCTCA TTAGCGGGCC CCACCTAATT TCCTTTTTTT 960 GATAGCACTT TTGAAGGTGC AGTGACTAGA TTTCAGGGAG GCTTTTAATC AAATGAGAAA 1020 CATGGGCTGA AAAATAACGT ATCCTGGAGG AATTGTAGCC AGGTGAACAA CCACAATGAG 1080 GGGCTCTTGT CAGCCATGCA GGTTGCTGGC AGTGGCTTCT GTGTGACGTG GCTGGGACTC 1140 TGATATGGTC TGGCTGTGTC CCCACCCAAA TCTTGTCTTG AATTGTAGCT CCCATAATTC 1200 CCACATGTTG CGGGAGGGAC CTGGTGGGAG ATCACTGAAT TGTGGGGGCG ATTTGCCCCA 1260 TACTGTTCTC ATGGTAGTAA ATAAGTCTCA AGAGATCTGA TGATTTGACA AGGGGTTTCC 1320 CCTTTCTCTT GGCTCTCATT CTCTCTTGTC TTCCGCCATG TAAGACGTGC CCTTCACCTT 1380 CCGCCAAGAT TATGGGCCCT CCCCAGCCAC ATGGAACTGT GAGTCCATCA 1430
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