Tag | Content |
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EnhancerAtlas ID | HS060-17735 |
Organism | Homo sapiens |
Tissue/cell | GM12891 |
Coordinate | chr19:35953220-35954410 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
E2F6 | MA0471.1 | chr19:35953967-35953978 | CCTTCCCGCCC | - | 6.62 | HLTF | MA0109.1 | chr19:35953889-35953899 | ATATAAGGTT | - | 6.02 | ZNF263 | MA0528.1 | chr19:35953755-35953776 | TCCTTCCCCTCTCTCTCCACC | - | 6.67 | ZNF263 | MA0528.1 | chr19:35953399-35953420 | CCTTCCTCCAAGCCCTCCTCC | - | 7.02 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_10065 | chr19:35952960-35954671 | CD14 | SE_60149 | chr19:35925812-35960098 | Ly4 |
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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 |
GH19I035461 | chr19 | 35952892 | 35954814 |
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Enhancer Sequence | ATGCCAAATA CATGTTTAAC CATGGAAATG TTTTAAAACT GTAATTCCAT TCTTCTGCTC 60 GAAGGCCTCC AGATACTTCT CATGATCCTC AGAGTAAAAT CCCATGCCTT CCCCAAAGCC 120 AGCAAGGCCC CTGATGCATC TAGCACTTGG CTCTCACCCA ACCCAGCTCA TCCCTACTCC 180 CTTCCTCCAA GCCCTCCTCC AGCTCCCTTC ACTCTTCCTT TTTTGTTACC GACAGCTCAC 240 TAAGCTCCTT CTCCTTGTGG TTCCCTTTTC GTGGAGCCCT CGTTCCCCAG GTACTCATCC 300 AGCTGAATTT CCCCTCTTTG AGGCTGCCTG TGACTCAAAT TTTATTTCCT CAAAGGACTT 360 CCCCCTCCAC CACTCCTAAG TGGCTTCCCT TTTGACACAT TCACATAATA CCTAGTTGCT 420 GACTTCGCTG GGTGTATCAT TAGCTGATAG CATCTATTTT TGTCTACTTG TTATTTTTAT 480 CCGTTAGACT TGCACATCCC TTAATGCATC AAATGGTTGA CTGTGAAAAA CAACTTCCTT 540 CCCCTCTCTC TCCACCACAG TCACTTACCG CTTCCTGGAG GCAGCTGCTG CTACCTCTTG 600 TCAGCAAAAT ATTTATCCCT CCATGCCTTT AAGGGGCTTG CTTATTTTAC TGTATTTCTT 660 CATTTCTCAA TATAAGGTTT CATCTGTTAA ATTATTCTGT GGCAGATGAA GATTATGCTC 720 TTATTCTTTT CCCAATATGT ACAACACCCT TCCCGCCCTG TCTTCCCGAT CTGCTCCCAT 780 TGTCACTATG TTAGAAAATA TTCAGTGTTT GCATAATCGT GACTACATCG ATGTTAATGA 840 CATTGGAGCT CTGTAGTAAA TAACAGCTCC TTTTTTTTTT TTTCTTGAGA CAGAATCTCA 900 CTCTGTCACC CAGGCTGGAG TGCAGTGGCA CGATCTCAGC TCACTGCAAC TTCCACCTCC 960 CAGGTTCAAG CAATTCTCCC TGCCTAAGCC TCCCGAGTAG CTGGGATTAC AGGTGCCCGC 1020 CACCTAGCCT GAATAATTTT TATTTTTAGT AGAGACTGAG TTTCACTGTG TTAGCCAGGA 1080 TGGTCTCGAT CTTCTGACCT GGTGATCCGC CTGCCTCGGC CTCCCAAAGT GCTGGGATTA 1140 CAGGTGTGAG CCACCGCGCC CAGCCAGTTC CTTTTTTATC CTGCACAACT 1190
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