Tag | Content |
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EnhancerAtlas ID | HS042-19455 |
Organism | Homo sapiens |
Tissue/cell | Fetal_brain |
Coordinate | chr17:43902180-43904230 |
SNPs | Number: 2 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NFIC | MA0161.2 | chr17:43903387-43903398 | TCTGCCAAGTA | - | 6.62 | PAX7 | MA0680.1 | chr17:43902367-43902377 | TAATCGATTA | + | 6.02 | PAX7 | MA0680.1 | chr17:43902367-43902377 | TAATCGATTA | - | 6.02 | Spz1 | MA0111.1 | chr17:43903748-43903759 | AGGGTATCAGC | + | 6.32 | ZNF263 | MA0528.1 | chr17:43902726-43902747 | CCCTCTCCTCCCCCCACCACC | - | 6.09 | ZNF263 | MA0528.1 | chr17:43902729-43902750 | TCTCCTCCCCCCACCACCTCC | - | 6.11 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr17 | 43903226 | 43903349 | chr17 | 43902406 | 43902572 | chr17 | 43903640 | 43903844 |
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Enhancer Sequence | TGTCTTGGCC TATGGGAGAC GTTCCATTCA CCTGCCGCCC CCTGTCTCTC ATCTCCCCTG 60 TGAGGTCAGG GGAGGTTGTA GTGTACACCT GGGGGAGTGA CCCGCCCCAC CCCCCAGCCC 120 ATCCGTGCCT GGCTCTGCCA TCTCTTTCCT CTGCAGCCCC TGCTGGCCTG GTGCCTAGCA 180 CTCTGGGTAA TCGATTAGTT TAATTAGTGA AAATGCCATT CCCTTCTGCC AGCCCCCAGC 240 CTCGCCAGAC CCCTCCCAGA ACTGCAGAGG AAAGTATCCA ATTAATTGAG TGGTAGGTTT 300 CTCAGCTCTG GGCCTGGGCT AAGCCCTAAT TAAGCTCCAG CGCCCTGGGG TATCGCAGAT 360 AATGGATTCG CAGAAGTCTG CCTGTGAAAT GGGACTTGCA AGGGCACCTC AAGGCCAGGC 420 ACCCCAGGAG ATCTGCCCGC AGCCAGCACC ACCAGGGGAC AGGCCCCCAA CTGTTGCATG 480 CATGGCTGGC CGGGGGATGG CACTGAGCCC CCAGCACCAC CCCTACACCT GCTGCCTGTA 540 TCAGCACCCT CTCCTCCCCC CACCACCTCC CGCTACTACT GTTCACTCCC TTCCCCACCG 600 TCCAGCCTTC CCCCACCCAC CCAACACTTG CACACACTCT ATCCCCTTTC CCCACGTTCT 660 GCTGCGCACA GGAGCCTGGG CCTCAGGCAC AGCCTGGGAG AGCACACCGT GGTGGGACAT 720 GAAACGGATT CTGGGGGTCT GGTTTGTGGA CCAAGGTTCA CTGCTCACCG TGTGGGGAGA 780 GGTGAGTGGT GGTTGGACCA GGGCTTCTGA ACTGCAGAGG TGCTTTTTCC TAAAACCAAG 840 CTCCGATTCC ATGGGCCTGG CGTAGGGCAT ACATTCCACT TTCCTCAAGA TCTCTGCGTG 900 CTCCTCTGCG TGCTGTTGCT GGGCCAGGGG CCACCCTTTG AGGATCGAGG GGCTGGAGTG 960 AGTGCCCACT GCAGGGTAAG AGGAGTAGCT CTGGAAGCCT CGGTGGAGAG GACGTGCCAG 1020 AATGGAGTGG GCACCAGTGG GGAGCTTGGA AGGGAGGTCT CATTGCCACC AACCCAGAGA 1080 GGCATCAGGA CGGATCTGGC ACTGCAGCGC CTGGGACGAG GTGGTGTCCT GCAGAGAGTC 1140 CAGTCAGAGT CAGCCGGGCA CAAATTGCTT ATTCAATTCA GATCACTGAG GGTACAGCGG 1200 AGTGGCCTCT GCCAAGTACC ACGCTGTGCC ACCCTCCTTA GGGCGGGGTG CCTGCTGGTC 1260 TTAGGTCTCC AGACTGGATG GAGATGGAGT GCTGGTCAGG GCCCGAGGGG TAGCTGTGCC 1320 CATTTGTCCT TCGGACATCC CAGCTGCTTT GCTGTTATCG TGGCCATCGG TCGGGGTGTC 1380 ACTGGCTGTC CCTGGGGGTG CTGCTGACTC TCCTCTCCAG GTATCACTGG CCACCTCTCA 1440 GGGTGTTCCT GGGTGCCTCT TAAGGCCTTG CTGTCTCTCT AAATAATGCT GGCCAGAACT 1500 CTGGTTGTTA TTGGAAATGT CACAGTGTCA CTGGCTTCTG TCTGGGTGTC GCAGGATGTA 1560 TTTGTCTCAG GGTATCAGCA GCCATCCCTC AGGCTGTCTC TCCAGCTGTC TTCTCAGGTT 1620 GCATGATGCT GATGTGGCCG ATGAGAGACA GGGCTTGAAC CCGGCCCAGG CCCGACTGCT 1680 CAGGGAGGCA CACTGAGACT TTGTCCCCCG GGAATGGTTT GGCCTGATTC TCCCTCAGGC 1740 TCTTGGAGGA AAGCCCTCTT GGGCGCTATT GTCCCAGCAG GAGGTCCCCC GAGGCTCCTG 1800 GGCCCAAAGT GGCGTGAGAC CACCCCAGAG AGTGCCTCTG CTTTCAATTC CTGCTTGTCC 1860 CCCAAGAAAT GTCGCAGGGG GCCGGACACG GTGGCTCACG CCTGTAATCC CAGCACTTTG 1920 GGAGGCCGAG ACAGGTGGAT TGCCTGAGCT CAGGAGTTCG AGACCAGCCT GGGCAACATG 1980 GCAAAACCCC ATCTCTACCA AAAAATACAA AATATTAGCT GGGCATGGTG GTGCATGCCT 2040 GTGATCCCAG 2050
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