Tag | Content |
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EnhancerAtlas ID | HS080-15729 |
Organism | Homo sapiens |
Tissue/cell | H9 |
Coordinate | chr18:20617220-20618160 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr2f6(var.2) | MA0728.1 | chr18:20617420-20617435 | GAGGTCAGAAGTTCA | + | 6.38 | RARA | MA0729.1 | chr18:20617420-20617438 | GAGGTCAGAAGTTCAAGA | + | 6.88 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr18 | 20617262 | 20617387 | chr18 | 20617684 | 20618026 |
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| Number: 1 | ID | Chromosome | Start | End |
GH18I023037 | chr18 | 20617681 | 20617830 |
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Enhancer Sequence | CTTTGGTCCA CTTCCTGGTA GCTGCTTGCT AACTCAAAAT CTCCTAGCAC TAGATACTGA 60 CCATTTGCAT CCCCATTGTT CCTGTAGATA GGATCTCTAA TGATAGATTC ATAAGGCTTT 120 TAAGAATTGC TTAAGGCCAG GCACAGTAGC TAATGCCTGT AATCCTAGCA CTTTGGGAGG 180 CCAAGGTGGT TGGATTGCTT GAGGTCAGAA GTTCAAGACC AGCCTGGCCA ACATGGTGAA 240 ACTTGGTCTT TACTAAAAAT ACAAAAATTA ATTCCAGCTA CTCGGGAAGT TGAGATAGGA 300 GAATCTCTTG AACCTGGGAG GTGGAGGTTT CAGTAAGCTG AGATTGCACC ACTGCACTCC 360 TGCACTCCAG CCTGGGCAAC AAAGCAAGAC TCTGTCTAAA AAAAAAAAAA AAGTTTCAGA 420 TGTTTTCCAG ATCCTGAATT CAATTGGAAT GGCTGATGCC AACCAGTTTG AAGACCCCCT 480 CAGAGGAACT GAATCAGCAT AAGAATACAG TTTCTTCATG TCCCTGTCCC ATGACCTCAC 540 CCAGCCCTCT TCAACCAATC AACAATCCCC ACACCTCAGC CCCCTACTCA TCCAAACCCC 600 TTAAGATCCC CAGCCCCAAA TTCCTTGGGG TTTGAGGCTT CCTCCCATCT CCTCACTTGG 660 CTGCCTGATG ATTAACCTCT TTCTCTGCTG CAGCTTGGTG TCTCAGTGTA TTGACTTGTC 720 ATGCACTGGG GAAGGAACCT GGTACGGTAA CAGAACCGCA GGTGTGGTGT TGTGAGAATG 780 CACATTTGAC CTGTGCTTTA TTCCTGGCTC TACTACTTAT CAGCTGTGGC AGACTGCCAC 840 AGTCACTACT TGAGACCATC ACTACAGCAG TTACTACTGT TACTACTTGA GACCCTCATT 900 ACAGCAGTTA CTGTTTCTGC CTGAGACCCT CATTACAGCA 940
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