Tag | Content |
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EnhancerAtlas ID | HS145-14747 |
Organism | Homo sapiens |
Tissue/cell | NHBE |
Coordinate | chr20:45529420-45530780 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ONECUT1 | MA0679.1 | chr20:45529456-45529470 | GATATCGATTTTAT | - | 6.31 | ONECUT2 | MA0756.1 | chr20:45529456-45529470 | GATATCGATTTTAT | - | 6.15 | TP63 | MA0525.2 | chr20:45530439-45530457 | AACAAGTTGTGACTTGTG | + | 7.17 |
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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 |
GH20I046900 | chr20 | 45529504 | 45530374 | GH20I046901 | chr20 | 45530381 | 45530530 |
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Enhancer Sequence | TTTAGATTGT GCAGGCCATT TTTTTAAGGT TACTTAGATA TCGATTTTAT TTTCTTGACC 60 CAAAATGAGA AAACACGGGG AATTCTCAAA AGCTTTTTAC AGGCTGCTAT TACGAGAAGA 120 GAAGCCAAAC CAACATGTAT TAGGTCATGC GCTTGAAGTG CATAAATAAG CCCTATGAAG 180 GTCACCAAAC AGGGTGAAAA CCACTAGTTC TCGTTACCTT GGCCACCTCT AAATTCCTGC 240 CTGTTAGACG TGTTTGGTTG AAGTGGACAC AGAAAGCGGG TTTCCGAGCC CGTGGTTGAA 300 AGATCTCAAT TTGACTTGGG TCCTCAAGGC GTCCTTGTGG TAAAGGGAGA TAGGAAGGCT 360 GAAATTCTGG TCTCCTCCCC ATGGCTCCCT CTCACGGTTC CGGAGAAAAA GCAGGTACTG 420 GGGCCTTCTC TTACTCCAAA GCAGATGTTT CCTACCTGGT ATTCGGATAT GCGGAAGTCA 480 GAAGCTGAAA ATAAAATGAA ATGAAAATGT TCCTTCTGGT CAGTTTCTTC ACCTCCCATT 540 CCCTTCCTAT AGTCACTTTG TGGTTAAGGT ATTCATGGTT TCCAAAACAA TTTTTTGTTC 600 CCACTATGTT TTCTAGCATT TAAGATGCAA GGTATAAGTA CTCACCTTTA AATCTCTATT 660 GATTGGCAGC TTCCTGAAAT ACAGAGTCAG AGAGCGTGTC CACCACGTCC TGAGTTTGGT 720 ACCAACCCAG GTGCTGATGG AAATTCCAAG TAGGGAGAAA ACGTCCTCTT CGGAGAGGCA 780 GGGTGTCAGC GCAAAGAGGT TATTTTCTTT TGTGGGTGTG TATTATTTGC ACATATCAGG 840 ACTTTTGTTT CAGGGTGTTC TAGAAACATT GATCTCTCCA GCAAAGTTCT GCGTGTCCTT 900 CTTGGTTGGG AAGGGAGCGG AGAGGAAGGA GCCCCGAGGA GAATCGTGCA CCTTTGGCCT 960 TTTGTGTGAC TCCTAGAGTA GAGGGAAGCC TCCGCTGCTC GGAAGGTGTC ACGTGGTATA 1020 ACAAGTTGTG ACTTGTGCCT GTGTTGTCAA CAGAGTTTTA GCCCCGTCCA GACATGAAAA 1080 AGAATGGAGC CCCGAAGATG ATTCACCTCC GGTCTGCGAT GGGCCCAAGC TGTCCAGTGC 1140 TCTCCTCTTG CTAAACAGAC CATACTCCCT GGAGGAGTTA ATGGCTGGGG TGTGGAGAGA 1200 AGACCGGTAG GAGGGGAGAA AGAATGCCTT AAACTCAGCA AATGTCTAAA ACGCTCAAAA 1260 TGTCTCAGCA TTGCTCAGGC ACCCACAAGA AAGACAAACT GATAAAAGGA CATAGAATCA 1320 GGCTTTTTTT GAGGGGGAAG CACAGAGAGG TTGGGGGTTT 1360
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