Tag | Content |
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EnhancerAtlas ID | HS003-12958 |
Organism | Homo sapiens |
Tissue/cell | A549 |
Coordinate | chr13:97165270-97166680 |
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) |
HSF1 | MA0486.2 | chr13:97166176-97166189 | GAATGTTCTAGAA | - | 7.52 | Mecom | MA0029.1 | chr13:97165575-97165589 | TTCTATCTTGTCTT | - | 6.42 | ZNF263 | MA0528.1 | chr13:97165411-97165432 | TGCCTTTCTTCCCCCTCCCCC | - | 6.11 |
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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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Enhancer Sequence | TCTGTTACAC CAATTGGATG ATTCTAAAGT TATTGAAAAA GAATCTTTTC CTTGAAATTC 60 TATGGACTTC TGCACTGTCA CATAGCTGTG TGTGTTGCTT TGGATAAATC TGAGATCAAA 120 CTGTATTTTT CTCTTTTTAA ATGCCTTTCT TCCCCCTCCC CCCTTTACTG GATGTCTGTG 180 TTATCTCTCT CCTTATCCTT GAAGTCCAGT GACTTTCCAC AATATATTTT GGCCTTGATC 240 TTTCTGTGTA TTTTTTTTTT CTGGGGCGAG ATCTAAAGAT TCCAGCCTTT ATTTTAGAAA 300 AGTTTTTCTA TCTTGTCTTT GAACACTTTT TAAAAATTTA TTCTTTCCCC TGTTCTCTGC 360 TTTCTGCTCA TTTGGGGTTT TCTTTTCTTT TCATGTCTGT ATGCATTGCC ATAATAATTT 420 AAATAACTTT GCTAATTTCC ATTTTGTTTC ATATAATTTT CACCATGATA CTGACATTTT 480 TAATGTATAT TAGTTCTAGT TTTTATAAGT TTGTATTTAT CTTTCCCTTC CACTTCTTGG 540 CTGAGCTCTG CCAGGTTACT TTTTATTTCC TTACATTGTC TTAAATATTC TTTGAACTCT 600 TGTATCTTTT CTTTAAAATC ATCATACTGT CTATAATTTA TTTGAGGCAA CAGAGAACTG 660 CAGTCATGTG TTGCTTAAAA ATGGAGATAC TTTCTGAGAA ATGCATTGTC AGGTGATTTC 720 ATTATGCACC ATCATAGAGT GTACTTACAC AAACTAAGGT AAGAGGATTT TTAAATAGGG 780 TGATGATAGA AGTGGTTCAG TAGGAGGCCA TCTTTGAGCA GAGGCCTATA TTGTTGAGAT 840 GCAATGAGAA GGAGACCTGT GACTATTGAA GGAAAGTTTC CAAGCAGAGA GGAGGCCCTG 900 AGACAGGAAT GTTCTAGAAG TGTGTGAGGA AGAATAAGGA GTGCAGTGTG GTTGTAGCGT 960 TGTGGGAGAG GAGAGTTAGG AGATACGCAG TGAGAGGGTG GGCAGGAGCC TGACCGTGAG 1020 CCTTGCGGGG CCTCAGTGCG ATGAGAAGCA GTAGGGATGT GAGTAGGGAA GTCACATGAT 1080 GTGGCTGATT TTTCAAATGG TCGCTGTGGA TGTGGTATCG AGAGTAGAGG AACAAGAGCA 1140 GAAGAGGGGG ACAGAGAGAT GAGTAGGAAT CAATTGTCAT AACCCTGAGA TTCAGTGATA 1200 CCAGCGTGCA GTAGGTTGAT GGAAGTAGAG CGAATGAGAA TTTCCTGGAT TTGGGCTTTA 1260 TATTGAAGGT GCAGCCAGCA GGATTTGGTG ATTAATTCAA TGTGAGATAT AAAGTTTGAA 1320 AGGAGTTCAA TTTCAAGGTT TTTCTCGCTC TGATCATTGG GATGAATGGA GATGCCATTT 1380 TCTACAGGTG GCTGCTGTGG ACTGAATTGT 1410
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