Tag | Content |
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EnhancerAtlas ID | HS108-20804 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr19:48394660-48396180 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
POU2F2 | MA0507.1 | chr19:48395566-48395579 | CTCATTTGCATAA | + | 6.44 | Pou2f3 | MA0627.1 | chr19:48395565-48395581 | CCTCATTTGCATAAAG | - | 6.6 |
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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 |
GH19I047890 | chr19 | 48393637 | 48396500 |
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Enhancer Sequence | TCAGGCTGGA GTGCAATGGC GTGATCTCGG CTCACTGCAA CCTCCACCTT CTGGGTTCAA 60 GTGATTCTCC TGCCTCAGCC TCCTGAGTAG CTGGGATTAC AGGTAGGCAC CACCATACCT 120 GGCTAATTTT TGTATCTTTA GTAGAGATGG GGTTTTGCCA TATTGGCCAA GCTGGTCTCA 180 AACCCCTGAC CTCAAGTGAT CTGCTTGCCT CAGCCTCCCA AAGTGCTGGG ATTACAGGCC 240 TGAGCCACCG TGCCCAGCCT GTTTACCTGC TTTTCTATAT GTGTGAGACA TTTCATTATA 300 AAATGAATAG ATAAAACCTA AACATGGCTC CACGTGGGCA CTGGCAGATT GGCTGGGATG 360 AGCTCCTGAG ATCTTATCTC CAGCATCTGG TTTGGGTTCT TTCCATGTCT GGCAGTAATC 420 TCTGGAGCTG GAAGAATCAC TTCAGCTGTG GCCCAGAGTG AGGCCTCTGA GGAGCTGATC 480 TGGGAGAAGA TGTCAATGTC CCCCCAGGGC TGAGATCAGG GCTGTGGATA GTGAGAGAGG 540 AGGTAGGAAG AAAGTGGTCA GACAGGCAGT TAGGGTGAGT CCTTGGTAAA ACTCCTTCAA 600 ACGAAGAACA GCCTGAAAAT CCAGCTGCAG GCCCCAGATA AGAAAGAGCT CACATCAGCA 660 AAATTTCTTC AAATCAAGAA CAGCCTGAAT ATCAAGCTAC AGGCCCTAGA TAAGAAACAG 720 CCCGCGTCCT TGAATGGAAA TGCCTGCTCT GTGAACCTAG ATAAACAAAT TCCACTCCTT 780 TTTTGGACAC ATTTTCCTCC CTTTGATGCA TGTTTGTCTC ATTTCACATG CTTCCTCTGG 840 ATTGATCCTT ACCTTTCACC TATTTTACAT ATACTTATCT TTCTGTGATT GGCCGTGGGC 900 AAAATCCTCA TTTGCATAAA GTGTAACATC ACTCCAGCCC CTAATTGGTT GCAGGCCAAG 960 CCTTCACCTC AGCCTCTAAT TGGCTCTTTT CACTGTTGTG TGTCTTTCTG AGTGGCCCAC 1020 AGACCAGTCA AGCACACTCC TCCCACTTCC CAGTCCATAA AACCACTGAA CTTAGCCCTG 1080 CAGCCAGCAA CTCTTTGTCG GGTCACCTCT CTTTGTTGAG AGCTTTTCTG TCACTTTCGC 1140 TTGATAAATC CCACTCTGTC CTACTCAGTC TCCAGTGTCA ACGTTTCTTA TTCTTCTTGG 1200 TTGTGGGACA AGAACCTGGA GCTTGCTGGT GGTGGGAGTA AAAGAACTAC AACACTCCCT 1260 CCCATTCACT GAACATCAGT AGTGAAAAAG CTGCAACAGG GCTGGGTGTA GTGGCTCACG 1320 CCTGTAATCC CAGCACTTTG GGAGGCCAAG GTGGGTCAGG AGTTTGAGAC CAGTTTGGCC 1380 AACATGGTGA AACTCCGTCT CTACTAAAAA TACAAAAAAT TAGCTAGGCG TGGTGGCGGG 1440 TGCCTGTAAT CTCAGCTACT TGGGAGGCTG AGGCAGGAGA AACACTTGAA CCCGGGAGGC 1500 AGAGGTTGCG GTGAACTGAG 1520
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