Tag | Content |
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EnhancerAtlas ID | HS067-03845 |
Organism | Homo sapiens |
Tissue/cell | GM18522 |
Coordinate | chr19:55116700-55118160 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NKX2-5 | MA0063.2 | chr19:55117372-55117382 | ACCACTTGAG | + | 6.02 | RORA | MA0071.1 | chr19:55116826-55116836 | TGACCTTGAT | - | 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 |
GH19I054606 | chr19 | 55117466 | 55119858 |
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Enhancer Sequence | GTTCTCCCTC CTCACAATAT TCCCCCAAAT ATGGTGAATT TTCACTTTTG GTGTCTCCAT 60 AGTGCATTCT GGAAAATTCT CCCAATTTTG TTTTCCAATT TAATAAATGT CTCTTTAGCT 120 GTATCTTGAC CTTGATAGAA TAAATATTTT GAGTGTGCTT CTTCAACTGA ATTTTTGCCT 180 CTAGGATTTC TAACTCATTT CTCTGATGCT CATTTTTTGC CAGTATAATC CATATTCTTG 240 TCTCAGAAAT TTAATTTCCT CTTGTATTTT TTTCAGATAT TTAAACATGT TTAATTGAAA 300 AAGGGTCTTA TGCGTTCCTA GTATTCTATT TCTTTGCACA TAATAATCCT TATCAACAAA 360 TGTGTAGACT GATGATCATA GCACTTTTTA TCATTAGAAG GATGGCTCTT GGTTGTCTAT 420 TTTTGTTGGA CACTCACCTC CTACACTCCT GAGCTACCAT GGAGGGATCC TCTCAAGGCA 480 GTTTTTAGTA ATCCAGGACT GAAAATGGGG GACTGTTCCA GCTACTGATG ACACGTGGCA 540 TTCATTTCCC AAACATAGTG TCTGCTCAGG TTGCTCCCAG AAGGAAAAAA ATGCATGTGA 600 AATTCACACT CATGGCCGGG CACGGTGGCT TATGCTTGTA ATCTCAGCAC TTTGGGAGGT 660 CGAAGTGGGC AGACCACTTG AGGCCAGGAG TTCAAGACCA GCCTGGCCAA CATGACAAAA 720 CCCCGTCTCT ACTAAAAATG CAAAAAAATT AGCCAGGCCT GGTAGTGGGC ACCTGTAATC 780 ACAGCTACTC AGAAGGCTGA AGCAGGAGAA TCACTTGGTC ATGAGAATCA GGCAGGAGAA 840 TCACTTGGGA GGTGGAGGTT ACAGTGAGTG GAGATCATGC CACTGCACTC TAGCCTGGGC 900 AACAAGAGCA AAACTCCATC TCAAAAAAAA AAAAAAAACT CATACCCACA CATGATACAG 960 ATACCCACAT GTAAGAACTC TGCAGTGAAT GAATTTGTTT CACACACACC CAGGGGAGTT 1020 GGCTCAGTGG TGGCCATGGG CCTGGGTCGG TAAATAGACA TATTCCATCA CAGCTTTCAG 1080 CCTTGCCCAG AGCCCTGGCC CTTCTCTGCC TGTGAGGACC CAGGGCCCCT TTTCTGTTCT 1140 GCACAGAAAT GGAAACTTCC TCCCTAATGA CCCCTAATGG CACCAGACAC AGATGCCCTC 1200 TCTGTTTCGT GTGTATCCTT CTCCTTCTGA TGAACTTTCA TTTCTCATTT TCTGGACATG 1260 ACTGTGATAA CCGGGGTGTT GATGAAATAT TATGAGAAGC ATCTCTCAAG GGCAGGAACA 1320 AAGGGGCTCT CCTTAGTGGA AACATCAATC TCAGGCCTTG ATGGTGGGCG CCAGCATCCC 1380 CTCATGCCCC CACCCCTCCT GTCTTCACCT GCTCTGGAAA TTACCCATGG CTGAGCCCCC 1440 TGCAGCCCCC AGGCTCCAAT 1460
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