Tag | Content |
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EnhancerAtlas ID | HS003-21492 | Organism | Homo sapiens | Tissue/cell | A549 | Coordinate | chr18:9513550-9515790 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr2f6(var.2) | MA0728.1 | chr18:9513560-9513575 | TGAACTCCTGACCTT | - | 6.04 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| | Number: 1 | ID | Chromosome | Start | End |
GH18I009514 | chr18 | 9514181 | 9514330 |
| Enhancer Sequence | AGGCTGGTCT TGAACTCCTG ACCTTAAGTG ATCTACCCAC CTCGGCCTCC CACAGTGCTG 60 GGATTACAGG CGTGAGCCAC TATGCCTGTC CTAGATATAT TTTAAATAAA CTTCCACTCT 120 AATTACATGT ACCAGCTGTC TTCTGGAAAC ATGTGAAGGC AGAGATTCTT GTTTGACTTT 180 TCTGTTCTTT ATTTTTCAGG GTCTCAGTTT TTGTATATTA GAGTTGTATT TTGGGATCTT 240 AATCTCACAA ATAAAAATAC TGAGTTTCCA GAAATGGAAA AGTTTTCTAG CGGATATTTC 300 CTGAAGTAAT AACTCAAAAT GATGTCTAGA AAGATATTAA GCTGGCCACA GTGGCTTACG 360 CCTATAATCC CAGCACTTTG GGAGGCTGAG ATGGGAGGAT TGCTTGAAGT CAGAAGTTCA 420 AGAGCCTGAG AAACAAAAAT TTAAACCATT AGCTGAGCAT GGTGATGTGT GCCTGTAGTC 480 ACAGCCGCTT AGGAGCCTAG GAGATTGAGG CTGCAGTGAG CTATGCTTGC ACCACTGTAG 540 TCCAGCCTGG GTGACAGAGT GAGACTCTGT CCTCTCCTCC GCTGACGCCC CACCCAAAAA 600 AAGGTAGATA CTGGAATTTT CCCCTTAAGG CATCTTACTT TTCTTGGGTA GGTCGTGTTC 660 GCTATTTGGG ATACACTTTT TTGGAACCTT CAATAAAGTA GCTATTTATC TTAAGCAAAT 720 ACCATGATAC ATTCCATTTG AGGTCCTATT CAGTAGGGAG GATGAATCAT TTGAGCGTGG 780 CTTTTTAGTA TGTTAAAAGC AAATAAAGTG AGTTATGTTA AGTATTCCTT ATTTTGAACT 840 TCATGACATT TTAAATTGAT TTGTTTTTGA AGAATTACAC AGAGTACACA AATTGTATAC 900 AACTTGATGA GTGGGTATGC CTGTGTAACC ACTACAAGGA TCTGGAAATA GAGCATTATC 960 AATTTTCTTT TGTGCCTCTT TAAAGGGAAT CACCTACCCC TCCCATAAGT AAACTTCTTT 1020 TATTGTTGAT TGATGCTGCC TGATTTTAAA CTTACGCATA CTTCTATTTG TGTCTAGCTT 1080 CTTTTACCCA ATATTATATG TTAAAAGTAA AACTTTTAGA CAAACTAAAT TTAATGGGTT 1140 TTTTTTCTTT TGTGTTTTTA TTTTGAGACA GAGTCTTGCT CTGTTGCTCA GGCTGTAGTG 1200 CAATAGTGTG ATCACGGGTC ACTGCAACCT CTGCCTCCCA GGTTCAAGTG ATTCTCCTGC 1260 CTCAGCCTCC CAAGTAGCTG GGATTACAGG CACCCGCCAC CATGCCTGGC TAATTTTTGT 1320 ATTTTTAGTA GAGACAGGGT TTCACCATGT TGGTGAGGCT GGTCTCAAAC TCTTGACCTC 1380 AAGTGATCTG CCCACCTCAG CCTCCCAAAG TGCTGGGATT ACAGGTGTGA GCCACCCTGC 1440 CTTGCCAGTT TAACAGAGTT TAATTGAGCA AAGAACGATT AGGGAATCCA GTAGCCCCTA 1500 AACCAGAATA GATTTAGAGC GACTCTGGGG CTGCCACATG GTCACGTAAT ATTTATGGAC 1560 GGAAAATGTA AAGTGACACA CAGAAAACAG AAGTGAGGTA CATAAACAGC TGGATTGGTT 1620 ATAGCATGGC ATTAGCCTTA TTTGAGCAGT TTGAACAGTT GCCCCCCTGT GATTGGCCAA 1680 AACTCTGTAA TTGGTACAAG AGTAGATTAC AGTCTGTGTA CACATCCAGT TAGGTTACAG 1740 TTCCCTATGT TCGGAGAAAC CTTTAGGCCA AACTTAAAAT ACATGAGGAG GCAGCTTTAA 1800 CCTAACATGT TTGTTAGATT GATTCATGTT ATTCCATGTG GCAGTAATTT GTTCATCTTT 1860 GCACTAGATA TTGTTTCATT GCATTATATG TTAGAGTTTA TTAATCTCTT CTACTTTTGT 1920 TGCTTGTTTG GGTGGTTTTC AGTTTTTGAC TGTTATGAAT AGTGCTTCTG TGGTGTACAT 1980 GTTTTTGTAT TTCTGTTATG TTTATGCCTG GGAGTGGAAT TGCTCATTTG TAGGCCATGT 2040 GTATTTCAGC TTCAGTAGAT CCCTGCAAAA CAGTCTTCCA GAATGCTTGT ACCAGTTTAC 2100 CTTCTCACCA GCAATGTATG AATATTCCAC TTGCTAAAGC ATCATGGTAT TTTGTCCTTA 2160 AGATTCTTGC CATTCTGGTT GGTGTGGGGT ACATGGTATT TTAGTTAGAG GGTAACTTAG 2220 GAAATAGCTG TTATCTTTTA 2240
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