Tag | Content |
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EnhancerAtlas ID | HS165-06844 |
Organism | Homo sapiens |
Tissue/cell | Ramos |
Coordinate | chr18:77384350-77385860 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MYC | MA0147.3 | chr18:77385810-77385822 | GGGCACGTGGCC | - | 7.22 | SPI1 | MA0080.4 | chr18:77385412-77385426 | AAAAACCGGAAGTT | + | 6.81 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr18 | 77385208 | 77385599 | chr18 | 77384640 | 77384762 |
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| Number: 1 | ID | Chromosome | Start | End |
GH18I079624 | chr18 | 77384325 | 77386000 |
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Enhancer Sequence | AGGTATTTTC ACATCTTTCT AGTCCTGGTG GAGACATTGA TTTTCCCTGA ATATATGAAC 60 AGTGCTTAGA TTTAACCCCG CTCCAAGCTT TGTGCCCTGG TGAAGCTGGC CGCTGCCACA 120 GCTCCAGGGT GTCACACTGC ACATGGTCTT CCCCACCTTC AATGGTCACT TGGGGCTGGA 180 GATGTGGCCT AACACTAGCC CAGTCTGACT CGCCTCCAGG CTCTGGCTTC TGGCACCTGG 240 ACAAGGAGAC CCTCACTTTC ATGGTCCCAA GGCACTGTCA GAAACCACTT TGTGGTGTCA 300 GGAAGAACCA GTCTCAAGAT AATGCAGAAC AGGGAGATTA AAACAAGACC ACGTGGTTGG 360 TGACATCACT GAGCTGCTGG GTCAAACCAT CGCTGAAGCC TTCTCTTCTG GATGTCAGCT 420 ACAGAAGCCA ATAGACCCCC TTTGTTACAT TATTATTTAA GTGAGTTTGA ATTGTCAGCA 480 ATCTGACTGA TACAGCTCAG TGAAAGTTGA AAGTTATAGT GTAATTTCCT AACACCTTGA 540 AAATCCTGCC TAGGCTAAAG GAAGCACTGA ATGGTGTCTT CTAAGGGAAG TCCTGCTGTA 600 TGGCTTGTAA AGATTGGCTA TTCGCAGGTT CCTGCGAGGA GGAATTTCAC TGACACCACT 660 GTTGCGGCAC TTATTTTTCT GTGCATAAAG ACTACTAATT TAGGACTTTA TATCCACCAC 720 AGAAAAGTCA ATTTTATGAG ACTGGTTCCT TTTTAAAGCC TACCTCTCTG CAGTAAGAGA 780 CTATTTAATA ATGACAACAA CAATATGCTT GTGAGAGCAA ACGAGGGTTG CAGCTCCAAT 840 TCAAGAGGCC AACCATGGCT AATCTTGAAG ATTTTCACTC ATTAGCTTTT TAAGGAGCTG 900 TTAACTGCAA ACGTGGGACT CAGAGCTTCG GGGACTTTCC GTGTTGAGTG TTCCGCCAGC 960 AGTGCTTGCA TGTCTCAGCA GCACAGAGCT ATTTCTGGGG AAAGCAGAAA TAATAAACTC 1020 ACTGAAAATA CCCATGATTG ATCCAAGCTT CCTCTTTCAA AGAAAAACCG GAAGTTCCTC 1080 CTTCCGTATT CTTGTGGAAA GCTTTGCAGG TGCAGGGCCA TGCGGCCGGG GAGACTGGGG 1140 AGCAGCCCTC CTGCCGCTGA CGGGTCAGGC CGGCTCCGTG AGTGATTAAT TCCCAGGTCA 1200 CATTTCTGTC CACAGCTGGG AGACGATGAT TAAAACTTGA GTGTGTTTAT TCCTTTGCAT 1260 TGGAACTTGA AAACATCAAT TTTTATTTCT TGGATAAGTA ATCAGAAAAG TAAAACAAGA 1320 TGAAAGAAAG GAGAGTTTGT GCTACGGACA CAGTCAAAGA CGTAGAAAGG CACAGTCCTG 1380 GAAGGAGTGT GGGAGCAGCT TGAGAGCAGA TGGACGGAAA GAGCCACAGT GGAGGCAGCC 1440 CAGAGACACC TGGAGATTAG GGGCACGTGG CCCAGGCCAC ATTTCAAACC ACAGGCAAGA 1500 GAATGGCTGA 1510
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