Tag | Content |
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EnhancerAtlas ID | HS034-09961 |
Organism | Homo sapiens |
Tissue/cell | ECC-1 |
Coordinate | chr15:52580490-52582400 |
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) |
KLF4 | MA0039.3 | chr15:52580658-52580669 | CCACACCCTGC | + | 6.62 | RREB1 | MA0073.1 | chr15:52581799-52581819 | CCCCAACCCTACCCCCACCA | + | 7.06 | ZNF143 | MA0088.2 | chr15:52580802-52580818 | TACCCACAAAGCAATG | + | 6.31 | ZNF263 | MA0528.1 | chr15:52581320-52581341 | CTCTCTTCCTCCTCCTCTTCA | - | 6.3 | ZNF263 | MA0528.1 | chr15:52581323-52581344 | TCTTCCTCCTCCTCTTCATTC | - | 7.01 | ZNF263 | MA0528.1 | chr15:52581317-52581338 | CCCCTCTCTTCCTCCTCCTCT | - | 8.17 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr15 | 52580530 | 52580869 | chr15 | 52581140 | 52581245 | chr15 | 52581798 | 52582070 |
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| Number: 1 | ID | Chromosome | Start | End |
GH15I052286 | chr15 | 52579180 | 52582470 |
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Enhancer Sequence | CTGAACTGCA ACCATCTACT TGAGAGTCCA TGTGCTCTCC TAACTATAAT TTAGGATTGG 60 TTTCAGCTAA AAGTGGTATT AAATGGCAGG CAGTATTAGG ACATACGTAA CCACTGACGG 120 CTTCTCTTCT GAAGACCAGT GACTCCTCAG CCCAGTACCC CAGGCCGCCC ACACCCTGCG 180 ATCCTGGTGC TTCTGCTGGC ATTGAGTGCC CTGCAGCTGA AACCCAGCCT GGTAAGTAAA 240 CAACGGTGAG TTTACTCAGC TCCGGGTAAG TTCCACCCAT TCATTCCTGT CCCCTCCTCC 300 CTCACATTCC TCTACCCACA AAGCAATGCT TCAAACTGGA GGAAGAGTTA ACTTTACAGC 360 ATTCATCCAA ACAGATGCAG TCCGCAGTTC ATGCAAACAA TGTAACCAGC TGTCAACTGA 420 CCTCCAGAAT ATGGGGCCTT CCCATGAGGC AGGAGTCTGT GGACTGGGAT GGAACAGCTC 480 GCCAAGCCCT TCAGCGGAGC CAGGAAAGAG AGGGCCACCT CCCAACTTCC CTGAGTGCCC 540 TCCCCATGCC AAGGCGCCAA GCTGAGGCAG AGGCTCGGGA CCACTGAACC TTATGAGCTC 600 AAGACCATGC CAGCCACCCC CCCAAGGCAC ACAGGTGAGA TGAGAACAGC ATCTTCTCAC 660 GCCGCCTGCT TTTCTGAGGG ATCTTCTGGC ATGAGCCACA GAAATGACTT GAAGACTTAT 720 ATGGAAGATG GGACAAGATG GGACGACATG TGTTTCCCTC CTAGAACCGC TTTCTGGACT 780 GGGAGTGTCC ACACTCCAGG TCAGCCAGGC CAGATTGTCA CACCATGCCC CTCTCTTCCT 840 CCTCCTCTTC ATTCGCTCCT CATGGGCCCC TCCCCTGGCT CCCCTGCCCC TCCCACTGCC 900 CCCCATGTCC GTGTCTCCCA AGGTCCTTCC CAGCCTCTTC TCATGATAGG CTGTTTCTGG 960 AGAGTTCCAC CCAATTCCAC AGCTTCTGCA ACTGCCTGGC ACCTGTGCAT CTGAGACCTC 1020 CCACCCAGAT CGTGCACTGG AGCTCTACAC CACATTTCCA ATTGCCTCCA AGATGTCAGC 1080 CCCTAAATGT CCTCATAGAC TCATAAATTC CAAACTCCAG TGATGCCGAC GCTCCTCCTT 1140 CCTAGCTCTC TTGCCCCTCA TGTCAGAAGC CTGGGACAGT GCTGGGCACC CCTCTGTGTC 1200 TCCACCCCAA CAGCCCAACA GTCACCAGGT GCTAGAAAAG ACTGCCTTTT AAAAGCCCTC 1260 TCCTGTCCGC CCCTGCCTAC CAGCCCCCTT GCCATGGCCA TAAGTCAGCC CCCAACCCTA 1320 CCCCCACCAA TCCTCTCTTG ACTGGTGCAG CAGCCCCCGG AGGCTTCCTC AGCCAGGCTG 1380 AGCACGAGGT TTCTTTGGGC AGACAGACTC TCTCATCCGT ACTTGATTGG AATTCCTGTG 1440 GGTGGGGCCC GGCAAGAGAA AAGCTTTGAA AATCAACCCC CACATGGGTT TTGAGGAAGA 1500 GCCAGGCCTG GGCAACCAGC ATTCTGGCCA ATTTCCTGCT CAGGCCTCAC CCTCTTTTCA 1560 ATCCACCCTC TGCCTGTGGC CACCCAAAAC CACTAGCACT TTCTGGAACA TGGCAGGCCT 1620 TCTTTGGCTT TCTGCTGTGT ACTTCTGTTC CTTCCACCCT AGCCCCACCC ATCCTCTCCC 1680 CATCCAAGAG CAAACAGCTC TGAACAGTCT GGAGTAGCTG GAGACACTCC TCATCTTGGC 1740 ACTCTCCTTG CCACTTGCCA TCTAGCAGAG CTGGATGCTT CCCTTGAGCG CTCTCTGCTC 1800 CTCCCCCAGG TATCTAGGCT GCCTCCCATC TCCCCCACTG GCATTTGAAC TTTAAGAGCC 1860 TGGTCTTTGT GCTTGGAATC CAATGCAAAG GCTTCCCATA ACTAGCACTC 1910
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