Tag | Content |
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EnhancerAtlas ID | HS037-03549 |
Organism | Homo sapiens |
Tissue/cell | ESC |
Coordinate | chr1:230887600-230888800 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ZNF263 | MA0528.1 | chr1:230888329-230888350 | GAAGGCTGGGGGAGGGGAGGG | + | 6.08 | ZNF263 | MA0528.1 | chr1:230887602-230887623 | GGGGGAGGGGAGGGGGAGGGG | + | 7.49 | ZNF263 | MA0528.1 | chr1:230887607-230887628 | AGGGGAGGGGGAGGGGGAGGG | + | 8.24 | Zfx | MA0146.2 | chr1:230888313-230888327 | CGGGGCCAGGCCTG | + | 6.24 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_32194 | chr1:230887396-230890088 | Gastric | SE_33557 | chr1:230879014-230891230 | H2171 |
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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 |
GH01I230750 | chr1 | 230885992 | 230891172 |
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Enhancer Sequence | GTGGGGGAGG GGAGGGGGAG GGGGAGGGGT CTGCGTGCCT CCCTCGGGGC TTCAGGCAGC 60 AGTCTAGGTT CACTTCAGGT TTGTCAAGAC CCCTGCAATT GAGACACCTC TGATCGTCCT 120 ATCACAGGAC TGTAGCTTCA GGTAACCCCT TCCTCATGGC CTCCCAAGCA ACATTTCACA 180 GGAACAAATG TACATCCAGG ATCGACACGC ACATGCAGGA CACTCACACG TAGACAATGC 240 TCCCAAGTGC ACATGCAACC AGCATACATG TGGAGCATGC ACAAGCACAC ACGTGTACCA 300 CACCTGGGCA CACACAACAA GGCAAGTCAC AGGCACCTTG CACATGTGGG CATGTGGGCC 360 GTCAGCATAC ACACCACTCC CAGGCATCTA ACCCAGGCCC ACCGCCTAGC TGCCCCTTCC 420 ACACATGCGT CCGCAGAACC CCCTGTGACT GGCACGTGTG CACACCAATT CCCAGAAACA 480 CTGACCCACA GAGGAGTCGG TCACACATCC AGACACCTCC CCAATTTATA CCCGATGGCT 540 AATTTGTGTT TACTTGGAGA GTTTCTGAGT TTTTTCCTTT TGTATTTTTC TCCTCATTGG 600 GTGCGATCTG GTTTAAAACA AAAACAAAAA CAGACCTCTC CTGAACAAAA CAACCAATTG 660 CAAGATAGGA GCTGGGAGGC GGTGGCAGCT GCAGGCACAG TTGGTACGGT TGGCGGGGCC 720 AGGCCTGCAG AAGGCTGGGG GAGGGGAGGG GCAGGGAGGA TGGGAAGGAG GCGGGCATCC 780 GGGAACAGCC CTGCCCCAGG AGCTAGCACA GCCTGCTGGG CAGGGATCTG TGGCTTTTGG 840 AGTACATTTT ATGTCCACTT GAGGAGTGAG TAGCATTGGC AGTGGGGGCA TTGCTTGCCA 900 GGGCTATCCC CTGGCAGGGG CTGGGCAATC AAGACAGGGA GGGCTTGGGG GACTCCTGGG 960 TTTCCCTTCG GGCAGGCACA TTCTGCAGCA AGCCCAGAAT GTCTAAGCTG GTGACAGATG 1020 AGGATGCAGC CGTGAGAAGT TAAATGGCCC ACCCTGAACC CTACTGCTGA GCGGGGCAGG 1080 CTATTCCTGG GACTCTATTG AGGCCCACTG ACATGGTCCT GGTTTGCATT GTCCTTCTGG 1140 GCTCAGCTCA GAGCCACCTG CAAACTCCTG CGCTAGCCAA GGTGGAGGAG GAAGAAGAGC 1200
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