Tag | Content |
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EnhancerAtlas ID | HS176-20722 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr2:62567840-62568840 |
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) |
Foxd3 | MA0041.1 | chr2:62568718-62568730 | GTTTGTTTGTTT | + | 6.32 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_32507 | chr2:62567019-62569023 | GM12878 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr2 | 62568148 | 62568365 | chr2 | 62568415 | 62568617 |
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| Number: 1 | ID | Chromosome | Start | End |
GH02I062340 | chr2 | 62567854 | 62568989 |
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Enhancer Sequence | GGATTACAGG CGCCCGCCAC CATGCCACCT AATTTTTGTA TTTTTAGTAG AGACGAGGGT 60 TTCTCCATGT TGGTCAGGCT GGTCTCGAAC TCCTGACCTC AGGTGATCCA CCCACCTCAG 120 CCTCCAAAAG TGTTAGGCCT GGCCGCAACT TCATATTTTT TTTTTTACCA AATGAGGATC 180 TGATTACAGA TCCAAAGAAT AAGAAGGTAT GTGGCCTCTG TTTGCACTTG CAAGTGTTGG 240 GGGCAATGAA ACTGTGTCAA TCAGCTTCCT TCTCCCCAGA GTCTGTTTTC AGGTTAGGCA 300 GGAGAACAGG GCAGAGTCAT TCCCAGAAGC CTGGGCCTTG TCAGATTCTT CAGAAGAGAC 360 GGCCTCCTGG GACACTCTGG ATCCCTGGCA GAGAGCTCAA CCCTGACAGC CTCCCTGAGT 420 CATACCAGAG CAGTCACTGG GTCCTGATGT CCCTGTTTCA GATGCTCTGC TCCCTGCCCC 480 CGCATCTCTG GAGTCATCGG GCTGCTGCAT GCCCATCAAC CTGAGTAGTT GCAGGCTATT 540 GGTGTCATTT CTGGAAAAGA AGGCAGCTGC TTCTCTGTTT GTTTTTCTCT TCCAACACAG 600 TGCCGTATTT ACCTACAGAA CCACCACAAA GTGACAGCCC TGGCAGATCT GCTACCATTC 660 AGCAGCTGCC TCAAGTCACC CAACATAGTG TTTGAGTCTC CAGTGAGAGG GAGGGAGACA 720 AAGGCTGCAT TCCACAGACC TGGTGATGGA GGCCCAGAGG AGAGAAGTGA TTTCCTCAAG 780 GTCACCCTGC TTCTCGGTAG CAGACCCAGG ATTCTCAATC TTTAGTTCAG ATGTTTCCCA 840 TTGTATGAAT TAGGAATACT GAACTGTCTT CACTTTTTGT TTGTTTGTTT GTCTTTGAGA 900 CAGGGTCTCA CTCCCCTTGC CCAGGCTAGA TTGCAGTGGT GCAATCACAG CTCACTGCAG 960 CCTCAACTTT CTGGGCTTAG GTGATTTTCC CTTCTCAGCC 1000
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