Tag | Content |
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EnhancerAtlas ID | HS098-26353 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr18:56160780-56162210 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
BCL6B | MA0731.1 | chr18:56161940-56161957 | TGCTTGCTAAGAATCAA | + | 6.22 | CTCF | MA0139.1 | chr18:56161204-56161223 | TGGTGCCCTCTGGTGGTTG | - | 7.78 | EWSR1-FLI1 | MA0149.1 | chr18:56162020-56162038 | CTCGCCTTCCTTTCTTCC | - | 6.46 | SOX10 | MA0442.2 | chr18:56161129-56161140 | TTCTTTGTTTT | - | 6.62 |
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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: 2 | ID | Chromosome | Start | End |
GH18I058492 | chr18 | 56159959 | 56161639 | GH18I058494 | chr18 | 56161690 | 56161866 |
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Enhancer Sequence | TCAGCTTGGC CGAGTGTGGG AGTCTATTTT GATCTTTTCT CCTGTTCATG GCCAGGACCA 60 GAGCTAGGCA CGCAGACCCC AATGGAGCCT GCTTTCTCAA GGCAACTGTC CTCCTGCTAC 120 ATGAATGAAT CATCCAGGCT TCTGTCCAGG GTCTCGGGAA TTTGGCTTCC ATGTCAGGGA 180 CGCTTGACAC AAGCCACACA TCCTTAAGCC TCGTCGTTCC TTCCTCCGAG GGTAGAAAGA 240 TGCAAGGCTG GCTGGCAGCC ACTGCGAGGG GTGTCCTTTA CGGCTGTCCA TATTAATCTT 300 ATTTTGGTCT AATGCTTACT GCCAGGGAAG AAATCTGCTA ATGGTACTTT TCTTTGTTTT 360 ATTTCAATCT GGCAACAGGA AATTGGCTTT TTAGGGGAGA CTACAAAGGG CAAAGTATTG 420 GTTCTGGTGC CCTCTGGTGG TTGAACTGCA ATCTCGTCGC CTCCCCGGGA ACTCCCCGAC 480 TGGCTGGAGA GAAGCATGAG TTTGCAGTTC GGCTCCACTG CACGCATGGC TTTAGATCGG 540 TCTGGAGTTG GTTAGGTTAC GTTTCCAAAT CTCCAGTTAT AAAATTAGGC CTTTTTTCCT 600 TGTGTAATTT CCAATTAGAA ATTTGTTCAA CGGGTTAGTA TCTTGGGTCT ATCTAGAAAA 660 TGGATTACTG GATGTCAAAA CAATCTTACT TGCCATACTT TGTAACCTGA AATTTTTGTA 720 CTCAACATTT GCCAAAAGAT TGAGGTGGCT GAGGCACAGG GGATGTGTTT CCAGACATAA 780 TTATATCTCT GGCTCCCAAG AGAAATATGA CATACTCCTG TTAAAAGGAA CATACAATGA 840 AGTAAAGTTG AATTAAAATG AGTAAGTCAT GACAATTCTC TATTTTATTT TATGAGATTA 900 GAGTAATTAC TCCTGAAATA GGATCATAGC CTTTGACTTC ATTGAACAAG ACAGCAAAAC 960 AGGTTGCATG ACTGGGGTGT CAGCAGCCAA ATATATGGTC CTGATTGAGA CATATGGGAA 1020 TTTTTTTTTT TAAATGACAC ACGGAGCACT GCTTCTTATG GTGGTGCTGT TCCCCCAGCT 1080 GAACCCTGCC AGGTACCAGC CCCCCCATAG AACTTGCGAC TCTCCCTTTG CATCATGAAT 1140 GAACTAAGCT CACTCACAGT TGCTTGCTAA GAATCAAGAG AACTTGCTCG ATCAACCCTT 1200 ATTCCTCCAT CTTCTCTCCT GCTGTCTGCA GTCTGCGATG CTCGCCTTCC TTTCTTCCCC 1260 AGCTCATTTG CCTCCCACCT GGACTTTCCT GTCTGCAGAG TGCCCTTGAA CTTGAGCCCT 1320 TTCCAAGTCT GTCCTCATGA GTTATCTCCC TTTTGCAGCT TTGACATTCA CTGGAGAACT 1380 TTTTCAATTG TGCCTCGCCT CCCAGCATTG AGGATCTGCC GTTCACTTTG 1430
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