Tag | Content |
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EnhancerAtlas ID | HS108-20628 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr19:45747290-45749370 |
Target genes | Number: 30 | Name | Ensembl ID |
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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) |
E2F6 | MA0471.1 | chr19:45748263-45748274 | TCTTCCCGCCC | - | 6.14 | E2F6 | MA0471.1 | chr19:45748747-45748758 | GGGCGGGAAGG | + | 6.62 | ZNF263 | MA0528.1 | chr19:45748383-45748404 | TTCTCCCCTGCACCCTCCTCT | - | 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 |
GH19I045244 | chr19 | 45748115 | 45749350 |
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Enhancer Sequence | CCCACCTCAA CCTCCCGAGT AGCTGGGAGT ACAAGTGCAA GTCACCACAC CTGGCTAATT 60 TTTGTATTTT TAGTAGAGAT GAGGTTTCGC CCTGTTGCCC AGGTTGGTCA ACTCCTGAGT 120 TCAAGCGATC CACCTGCCCC AGCCTCCCAA AGTGCTGGGA TTACAGTCAT GAGCCACCAC 180 ACCCAGCCTT GATTTCTCTT TCATCCTCTG AACTGGCATC CACATGCCTC ATCCCAAAAT 240 GGCTCCATCA TCCCCCCTCC ACCCCATAAC TGTCTCCATC TTCCTCTCAA AATTTCAGGC 300 TCGAATTTCC CTCCAATTGA AGTCAACCTT GCCCGGACTA CATCTGACTT TCCCCCACCT 360 GGCTTCAATA TCGCCTCCAA ACTGGATCCA ACATCCCCAA ACCTGGCTGC AACATTTTCC 420 CAAAACTGTC TCCGACGTCT TTCCCCTTCC TGGCTCCAAC ACCCGCCTCT GCAAACTGGT 480 GCTGACATCC TGCCCCCTCC AACCCTCTGT CTGCCTCCCA GTGCCCAGCC CCTGACTCAC 540 TTCCGAGGCA TCCCTCAAGC CCCCAGCCTC TCAGGCCCGC AGGATGTCTT GGCCACCAGA 600 GCTTCCCTCT TTGAGCCCCT CCTCCTCTTC CTCACTGCCA GCCTTTTCCC CGGAGTCCCT 660 AACCTTCTGC AGCGGCCCTG ACCTCGGTTT GCGGAATCCA TCACCTCCAA CGCTCAGCAT 720 CTGTATTAGA GAACGGTCTT TCCATATGGC ATGTCCCCAA GCCCAACCCC AACCAGTGCA 780 ACCCCAATCT AGTCCTTGAC CCCAAACACA ATCCTGTCAT CAGCCCAGAC CACTGCAAGC 840 TCATCCACAT CTCCAATCCC AACCTGATCT CGGTCTCTCC TGCTTGATCT CAATCCCTAC 900 CTGGTCCCTG TCTCCCATCT CCGAGACCCC ATCTCTTGGG ATAGAACAAA TACCCGATCC 960 TTCCTGGCCT CAGTCTTCCC GCCCAGACTC GCAGGACATT CGACCCAATG TCATCTCATC 1020 TCTATTCTCC TTTGGTGGCA CCAAGGTTTC TAATGCTCCC TTGCACCCTT TGTGGACCCC 1080 GCGAGTCCTC AAATTCTCCC CTGCACCCTC CTCTCATTTT CATCTCCTTT CTGCCTTCTC 1140 GCCAGCACCC CTCTGGAGTC AGGCCCCAGA TTCTCTCTTT GCCCCCAGCC TCTGCTGGGT 1200 TCAAGGTACA GGTTCTCATC AGCTCTGGTC CAGTGCAACT AAGGGCAACT GTTTTCCCAG 1260 TTGCCCTGGG GAAGGGGGAC CCCTTCCCCC TGTCCCCAGC ACACTCACCT CTGTCCTCCT 1320 GCCCGTCCTT CTGTTCCCGC TGCTGTCCTG TCCCCAGGCT ACTTCAGCCA GGACTGCTGG 1380 GAGCTTGGAT CTGAGTTGGG GGGGTGCTCG GAGGAGGACA ATTTCCTGTC AGGAAACCCC 1440 TCCCTCTCTG GGGCCAGGGG CGGGAAGGAC TCATTATCTG TCTGCCCTTT TAGGCCAGGC 1500 TGCGGTTGGG CTGGGAAGGC CGAGGCCCAC AGCTGGGCCC CCACCCTCAC CCCCGCTCCA 1560 GGCCGGAATC CGCCCACTCC TGCATGCTCT TCACGCCTCC CAAGGTGACA ACACCATCCT 1620 GGGCGCCCCG GGGAGACACC CCAAGCTGGA CGCCAGCCCA GAGCTGCTCT CCAGCATGGG 1680 CAAGCCCCGA GGCCTTAGAA TGAGAACCGG GGGGCAGGCA CGCATCTCTC TAGAGTTCCC 1740 TGCCACGGGC TGAAGACCAG GAGGGAAGTT TTGCTGGGCC CAGGGGCTGG GGAGGGGGAC 1800 CTATGGAGGA GGGCACTGGA CATGGCTTTG GAATTGTGGT TCTCTTTGTC TAGAAGCCCC 1860 TGTACCCAGG TCTCTGCATG AGGCCCTCCT TTTCATCATC CCAGTTCCAG CCCCACAGTC 1920 TCTTCCTCTG TTCTCCACTG TCCCGTCTCA CAGAGTCGTC ACTCTGCTTT GTCAATTTAT 1980 TTTTCTTTTT TTTTTTCCTG AGACAGAGTC TTGCTCTGTT GCCCAGGCTG GAGTGCAGTG 2040 GCGTAACAAT AGCTTACTGC AGCCTGGATC TCCCAGACTC 2080
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