Tag | Content |
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EnhancerAtlas ID | HS047-14390 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr17:37400200-37401710 |
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) |
CTCF | MA0139.1 | chr17:37401167-37401186 | CCCTGCCCCCTGGTGGCCA | - | 7.81 | RREB1 | MA0073.1 | chr17:37400258-37400278 | TGGAGGTGTGTGTGTTGGGG | - | 6.86 | ZNF263 | MA0528.1 | chr17:37400523-37400544 | TCCTCCTCCTGCTGCTCCTCC | - | 8.06 | ZNF263 | MA0528.1 | chr17:37400520-37400541 | CCCTCCTCCTCCTGCTGCTCC | - | 8.09 |
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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: 2 | ID | Chromosome | Start | End |
GH17I039244 | chr17 | 37401081 | 37401270 | GH17I039245 | chr17 | 37401361 | 37401510 |
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Enhancer Sequence | AAACAGCCCC TGCATGAGAG GGACAAGTAT CAGACCGCCT GCGAGAGCAC TGTCTTCTTG 60 GAGGTGTGTG TGTTGGGGCG AGAGCAGGAG GGGAGAGTTG GAGAAAAGAT CCTCACGGTA 120 CAGATGGGGA AATGGAGGCC TCCAGGGCTC TGACTGCTGC AAGCCCATCA CAGCCCCCTG 180 GGGACTCCAC CACTTCCTGC AAAGGACACT CTCTGCCCTG TCTGTGGTTG TTGAAGCTTC 240 CAGGAGCTGA CGCCCTCCAG GCTGCCTGTC CTACGCGGGC CATCGCCACC TCCTTCCTTG 300 TGTGCTCCCT CTGCCTGGCC CCCTCCTCCT CCTGCTGCTC CTCCTGGCCA GCTCCTCCAA 360 GGCCCTTCCT CACTGCCCCA GGCCCGCCGG GTGGTTAACT TCTTCCTTCC TGTGGAAACC 420 CAGTCCACTT GTCAGGCCCC TGGTCAGCTC TTAATATACA GGTGGAGAGA AGGGAGCAAT 480 GACCAGCCTT GCTGTGTGTT TGCCTGCAGT GTTCGCCATG GCCGGAGTCC CCTGCAAGGC 540 CCCGGCCACC TCTCAGCTCT CTGGCTCTGA CCTCTCCCCA CTCCTGCAGG CTCTTGTCCC 600 CAGAAAGGTG AGGCAGGATG AGCACCTCCT GTCAGCCCTT TGGGGTGAGA GTGAAGAAAA 660 GAGCTCCCAG CCCAGGCATG GAGCAAAGGG CAGGGCTGGG GATTGGTGGG GAATTTGTGG 720 GGTGAGGACA GGAGCAAGCT CTGTGTCCCA GGGCAGGCCT GGAGGAAGGG TGTTGGTGGA 780 GGGAGACTGG CTGTAATGCT CCGCAGAGTT CTTGAACCTT TGCTCCTCCT CATAGGCTCT 840 GTTCCTCACC ACCATTCGCT CTGGATACCT TGGGGTGTAG CCCAGTTGAG GTGAGCCTTC 900 CCCTTCCCAC TCTCCACTGT CCCAAAGCCT TCTCCGCAGC TTCATCTCAA GCTCCAGAAT 960 GGAGTGGCCC TGCCCCCTGG TGGCCAGATG TGATATGGCC ATAGATTGTA ACTTACCTGA 1020 TAAGACTGGG CAGGAAGAGC CTCCCTTCTC AGACTTGGGA CCTCCCAAGG GAGGGGCTGT 1080 TTCCCTTTCT TGTTCTGTCC CTGGGTCCTG GTATTACCTG GACCATCCAT TTTATACCTC 1140 AGGATCTGAA CCAAAAAGCC CCCATCTCAG AGACACAGCA ATGGTTGCAT CAGCACTGGT 1200 TCTCCAGCTA CTGCCGGATG CTGGCCAACT TCACTGGTGA GGCTAGTGTC TGGCAGGAGC 1260 CAGACCTGTA GGGGACTGAG AGTGGGTGGG ACACACAGGC AGGAAGCCTG TCTCTGTCCT 1320 GGCTTGTTGT GGGCCCTTCA ACTAACATTT ACTGGGGACT AAGAGTTGCC CAGCATTGTG 1380 CTAGGCTCTC GTCTCACGAA TTATCCCATA TAATTTATAC ACTATTCCTT GAGGACAGTG 1440 CCCAGAGAGG TTAAATAACT TGCCCAAGGA CACACAGCTA ACAAGTGGCA GAACTGGCAT 1500 TTAAATCCAA 1510
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