Tag | Content |
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EnhancerAtlas ID | HS118-04952 |
Organism | Homo sapiens |
Tissue/cell | Liver |
Coordinate | chr12:117950530-117952910 |
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) |
POU2F2 | MA0507.1 | chr12:117951927-117951940 | ACATGCAAATGCA | - | 6.37 | ZNF263 | MA0528.1 | chr12:117951313-117951334 | GGGGAAGGAGAGGGAAAGGGA | + | 6.22 |
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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 |
GH12I117514 | chr12 | 117951961 | 117952110 |
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Enhancer Sequence | AATAGACTTA GAGGCACCTC ACATTCAACA TCCCCAACCA AAATCTCCTG ATTTTGCTCC 60 CTGAGCCTAA CTTCAGTATC CTGGTCCCAA CCTGACATCA TGTCCCACCT TTCCCTCCTC 120 TATTTTCTTC CAGTGACACC AGAAGGCCAA ACATTAACAG AACCTTGCTG CCCATAGGCA 180 GAAGGGATTT CTGGGCACTG GACATCTAGA CAACAAAAAA AGCAAACACT AAATACAGTT 240 TCTCTTGGAG GAAAACCTCT CCTAGGATTT CTGTAGTTCA CCGCCCACCC CTCCCCCCGC 300 AAAAAAATCA GTGAGCACCT ACTTTGTGCA GGTGCTGTGT TTGAGTCTGG GGATACTGAG 360 TCATTCTGTC TGTCCTCCCT CCATCTCGTT TCCCTCTTCT GCCAAACAAA TTCTTATGTC 420 ACAAAGATAT ATGATCTCAA TGCATATATT AATACATCTA TTGATTTTCC TCTTGCCAGT 480 CATTATCAAG ATTTATTTAT CCTCACAGCT CTCCATTGAT TGAGGAAAGC AGTATTCCCA 540 GTGGTCAATC AATCCTGATA TACTCCATGA CAAGGAGTCA ATATCTATTT ATTATTTGAT 600 TTATGGACCT AATTATCTTA AACATGATCA GGCAGGGGGC AAGGCCAAAG CTGAGCAGTG 660 ATCAAGCAAC TGGAGCCAGG TTGGGAATAC ATCAAACCAA AGTCTGGGGC CCAGCAAGTT 720 TCTGAACAGT GCAGACACAC TGATTTTACC CTTCCCACTC TCACCACCCC AGCATCTGCC 780 GCTGGGGAAG GAGAGGGAAA GGGACAAGTG GCAGGGTTTC AATTTGTGCC TGCTGCCAAC 840 TCAACAAGTC ACAAGCCAGG CAGGTTTGGT GGTTTGGACA ATGAACCTGA TTTGGAGGTA 900 GGTCAGTTGT TGTCCTTCCC AGGGAATGGG ACCCAGCAGT GGGGAGTTCT TAAGGTGTCC 960 GTGGGACATA AGAAAGTGGG ATGGACTCAG GCACGGCTAG AAAGGGAAAG AGGACGAGAG 1020 AGTGGATGGA TACAAGCTTC AGTATGAATC AGACAGTCTC TTCCTAGCTT ATGACCTTGG 1080 GCAAAATCGT AATTAAAAGC TGATTCCCTG CAATCTGACC AACCTGCATG AATTACTGGT 1140 TTTTCTGTTT TTTGAATCTC TTTCATGATC CCTTGAAGTA GGTACCGTTC AATTCCCCTA 1200 TTTACAGACA AGGAAATGGA TTGCATGGTA CCTACTTCAG AGGGTTGTTA ATTACAACGT 1260 TGTCTCCCTA TGTAAAGCTG TCCCCATACT CCCAAATCTT TGTTTAACCA CTGCCTGCCG 1320 GCAATACTGA GGAAACCATC CCTTTGCTTT CTGGAACACA TGGTAAGGGC CCGATGTTGC 1380 CCACACTTGC CTTCAAAACA TGCAAATGCA GCTGGCTATT TTTAACGTTG GTAAATAGTG 1440 AAAGCTGTTG AAAATGCCTT CATTTCCAAA GGCCTGCCAA CTCCCTGTTG CTTTCCCCTA 1500 CGGGAGGCAT GCCAAAAATC TCTTAGAACC TAGGGCATTG AAGCCTGCAT TTGTTCCTGC 1560 TAATGTCTGA TTAGGAGCAA CACTAACCGT CCACACCATT TTTGGAGGAG GGGAATACAT 1620 CACCAACCCT ACTGCAAGCT CTCTTAAGAA GAGGGAATGT CCCAAAATAG TCTTTATAAA 1680 ATGCAAACCA GACTGTGTCC CTCCTCTGGT TTAATCCCTG GGTGGCTCCC CTGACTGCCT 1740 TTGGGAGAAA GGTTCAAGTT CCTTAGCCTG ACTTGAAAGG TCCTTTAAGA TGTCTTTGGT 1800 TTCTCTCTCT CTCTCTCTCT TTTTTTTTTT TTTTTTTGAG ACAGGGTTTC ACTCTGTTGC 1860 CCAAGCTGGA GTGCAGTGGT ATGATCATGG CTTTCTCACT GCAGCCTCAG TCTCCCAGGC 1920 TCAAGCAATC CTTCTGTCTC AGCCTCCCAA CTCGCTGGGA CTACAGGAGC ACACCATCAC 1980 ATCTGGCTAG TTTTTTAATT TTTGTAGAGA TGGGGTGTCC CTGTGCTGCC CAGGCTGGTC 2040 TTGAACTCCT GGGCTCAAGA GATCTTCCCA CCTTGGCCTC CCAAAGTGCT GCAATTACCG 2100 GTGTGAGCCA CCGCACCCGG TCAGATCTCT CTAGTTTCAT ATCTCTTGCT ACTCCCCGTA 2160 TATATCCTCT ACTCCAGCTC TTGCCCCTCC CCTGGCCTTG CTACCTCCTA CCTCTAAGCC 2220 TTTGCATATG CTGTCCCCTC CATTAGGAAT GTCACTCCCT TCTTGTCCAT CTGCCTAATT 2280 ACTTGGTTGG ATAAGGGGCA GGTTCCAGGT CCCCATGTAC CCCTGGGATC TTATTGCAGA 2340 GATCACGACA CCGTTGGAGA ATCATCCAGT TAATTTCCTT 2380
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