Tag | Content |
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EnhancerAtlas ID | HS176-02418 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr1:153478920-153480120 |
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) |
ZNF263 | MA0528.1 | chr1:153479529-153479550 | TGAAGAGGGGAAGGGGGAAGA | + | 6.03 | ZNF263 | MA0528.1 | chr1:153479781-153479802 | CCCTCCTCCCACCCATCTTCC | - | 6.16 | ZNF263 | MA0528.1 | chr1:153479784-153479805 | TCCTCCCACCCATCTTCCTCC | - | 6.53 | ZNF263 | MA0528.1 | chr1:153479769-153479790 | CCCCCCATGTCTCCCTCCTCC | - | 6.86 |
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| Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
SE_02992 | chr1:153478832-153481149 | Bladder | SE_28418 | chr1:153478695-153480927 | Fetal_Intestine | SE_36529 | chr1:153479156-153480743 | HMEC | SE_52579 | chr1:153478743-153481142 | Small_Intestine |
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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 |
GH01I153506 | chr1 | 153478735 | 153481271 |
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Enhancer Sequence | AGCTACAAAA TCCTTCTTGC TACATCACCC CTGTACGCAC AGCCACATGG CACCCAGGTC 60 CACATGGGCA GTGAGCCACC ACCTCTCATC TGCTTCCTCT GTCACAGGAC TACAAGGGGC 120 TGAGCAAGGT AGGCATGGTC AGGGTGCCAG GCATCAAGGG ACAGGGCTAT CGGATCAGCC 180 GGGCCTGTGC TGTGACAGGT AGGAGTGAGG CAGTATGATT GGGAGCACCA CCAGCACCAC 240 TAAAAATGGG GAGAGAAAGT TCCGCTAGGA ATGGGGTTAT CAGAAATGGG AAGAGACGGT 300 GGTCAGACCT GTGTGGGTGA AAATGAATGC AGGAATGACA CCAAAGACCG GCTAGCTTCC 360 ACAGCCCTTT GCAGGATGCT CTGAACTTGC TGAGCCCTTT CACACCCGCC ACCTGGTCCC 420 TGTTGACCCA CCAGCTGTAT GCAGCTGACT ATCTTCACCA GCTCCTTGAA CAAGAATTTC 480 CATTTCCAAG GCCAGGGTGG GGGAGGCTGC AACATTTTTT GCCAGAGAAT CCAAAGAGCA 540 CATGAGTCAG CTGCCTGGGT CAAGGCCCAG ATCCCTGTGG CGGGTCAGCC AGAGAGCAGG 600 AGCTGGCCCT GAAGAGGGGA AGGGGGAAGA AAGAAACCCA GAGGGCTCAG AGAGCACAGG 660 ACCCTGCCCA CGTGGGCCAC TCTGCAGAGG CCAGGCCCAA GGCTGAGTTG GGCCTCCCAC 720 ACAGACATGG AATGAGAAGG CTGTCAGTGC AGGACAGGGT GAGGACACAC TCAGCGGGCA 780 CGGCTTTCTC CCCTAACAGC CACTCCACCC AGGGGCCAGA AACTGACTTC ACCTCTGCAC 840 TGAATTCCTC CCCCCATGTC TCCCTCCTCC CACCCATCTT CCTCCTGGTG CTTCCAGCAG 900 AGCCAAGAAG GCTTCGCCCC ACCTACTCCC CTCCTGCTGA CACGGACCCC CCACACACAC 960 ACCCAAGGAA CAGGAATACC AAAAATGATA CTACCAGAGT GAAGCGTGTC CTGCAGACAT 1020 TATCTCTTTA ATCCTAACTA TAATAGTCCC TATTTCAGAG ATGAGGCAAA TGTGAGAGAA 1080 CAAGTAACTT TCCCAAGAAC ACACAACCAA GAAAAAAGAA AGCCAAGATT CAAGTGCAAG 1140 TCTGCCTGGG GGTCTGGAGC CGGCTCCCCT GCTGCCCCCT GCCATCCCTC CCTTCCACTC 1200
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