Tag | Content |
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EnhancerAtlas ID | HS108-20301 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr19:38612780-38614030 |
Target genes | Number: 11 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
GLI2 | MA0734.2 | chr19:38613768-38613783 | CACCTTGGGTGGTCT | - | 6.25 | REST | MA0138.2 | chr19:38613627-38613648 | CTCAGCACCTGGGCCAGCATC | + | 6.93 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_65256 | chr19:38612554-38613976 | Pancreatic_islets |
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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 |
GH19I038121 | chr19 | 38612555 | 38613976 |
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Enhancer Sequence | AATCCGAGAG GCAGAGGTTG CAGTGAGCTG AGAGTGAGCC ACTGCACTCC AACGTGGGTG 60 ACAGAGCAAA ACTCTGTCTC AAAAAAACAA ACAAAAGCAA ACTCCTGTGT TCCTCCCCAC 120 CCCTCTCAGA GGTTTCCTGA CTTTGTAAAA TAGAAGTCCT CTACTCAAAT AAGGTTTTAG 180 GGAAAAAAAG GTCGACTCCA TCCCTCCATT TGCGGATGTC AGAGCTTTGG CATCAGCCTG 240 GGCTCCACTC TCTCTCATGC CCACATTCGT CAGCTCCACT TCTGTAGGCA GGCATCAGCC 300 ACCTCTCCCA GAGCCCTCAC CCTGGAGCGA GCCACCCTGG TCTCTCCCGG ACACTTTCGA 360 TGGTGTCCTT TCTGGTCCTT CTTACCCCTG CCCTTGCTTC TCTGTGGCCT GTTCTCGACG 420 TGGTAGTGAG AGCAATCTGA TCACATCACC TCTCTGCCTA AACCCTCAGG TCACTCTAGG 480 TTAAAGCCTC AGTCCTTACA GAAGCCCATG AGGCCGGGTG TGAACTGGCT CCCTGTCGAC 540 TTCTCTGACC TCATGTCACT GTTGCGCTCT CTGCCCCAGC CATGAAGACC TCTGAGGTTT 600 CATGCGCATG CTAGGGCGGC GTCCAGCCTC AGGGCCTTTG TACCACCTCT TGCTGGAACA 660 CTTCTCTGAT CACCACATGG CTCGCTCCCT TTCCTCCTAC AGGCCTTTGG TCACATGTCG 720 CCTTGTCGGT GAGGCCTCGT TATCTAAGAT TGCACACCCC CTCCCCTGGC TTGGAGCACA 780 TTCACGCGCT TTGCCTGCTT AACCACCATC TGCCATGCAC TGTGTGTTAT CTGTTCACTG 840 CCGTGTCCTC AGCACCTGGG CCAGCATCTG GTGCACAGTA GCCGCTGAGT GAGCAGGAAC 900 CGAGTGCAGG CACAAATGCG TCGTATGCTA TAGTGGCCGC AATAGTGAGG ATCAAATGGG 960 CGCCAGCTCT GCGTCAGACC CTGCTCAGCA CCTTGGGTGG TCTTGCGTCT CTTGCTCACA 1020 AAAGCCTGAT GAGGTCCTCA CTTCGCAGAT GAGGAAACTG AGGCCCAGAG ATACCTTGAC 1080 TTGCCCAGAG CCCAAAGAGC CTGGGTTTTG GAGTTTTTTT TTTGTTTTTT TTGTTTTTTT 1140 TTTAATTGAT CATTCTTGGG TGTTTCTCAC AGAGGGGGAT TTGGCAGGGT CATAGGACAA 1200 TAGTGGAGGG AAGGTCAGCA GATAAACAAG TGAACAAAGG TCTCTGGTTT 1250
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