Tag | Content |
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EnhancerAtlas ID | HS183-03887 | Organism | Homo sapiens | Tissue/cell | T47D-MTVL | Coordinate | chr3:195478140-195479240 | SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
| TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NFIA | MA0670.1 | chr3:195479022-195479032 | ACTTGGCACC | - | 6.02 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr3 | 195478515 | 195478752 | chr3 | 195478180 | 195478230 |
| Enhancer Sequence | ACCTAGGTTA GAGGATGGCA GATGGGGGTG GGGGTGAGGC CCCATCCGGG GGGGAGACGC 60 CCTCCCACCT TGATGGGTGT ATTCATCCCT GTTTCCTCCT GGAACGGGAG CCCCAGGACC 120 CCAGCACCTT CCTCACCTGT CTCTGCACCC TTGCACTCTA GCCTAGCTCA GTGAGTGTCA 180 TGGGTCCTTG CTTAATAATG TTTGTTGAGA GTGAAGGGTT TTCCATTCTG TCCCCCCCTC 240 AGCCTCATAT GACGAGCAGA GAATCTGACA TGAATGGCCC CTACCTTGCC TCTGACACAT 300 GACTCATGAC CTCCTCCCCA GTATATTGAA CATGGGTTGT TTAGACCTAG GAGATGGTCG 360 GGGCTGGGGG TGTCAAGGTG ACTTAGGTGG AGTCTAAACT CAAAGAGTGC ATTGTCTGGC 420 GCAGGTGACA AATGTCAACA GATTTTACCG TGTGGAGTGT GGAGTGGGGA GTGCTAGGCT 480 TGCAGTAGTG ATAATAGCAG TCATCATGTT TGAATACTTG TGTGTCAGGC ACTGGACTAA 540 ATGCTTGACA CGCGTTATCA TTTAAACGGT GATACGGCCT GTTGACTCAG GTGCTATGAT 600 TGTCCCTGTG TTTACAGATG ACCTGTTATA TGATGTGTCT AGTTAGCACA CCTGCTCTAG 660 TGAGGGGCAG AGCAGGGATT CTGATTCTGG GTGTGCAGGA TTCTACAGCC CCAACCACTC 720 AGCAGTTGTG CCACTTTGCC TGTGACTGAG GTATGGCATG GCAGCCAAGA AGAGGGAGCC 780 GCCCGTTCCC TCTGGGAAGT CAGGGAAGAC TCCCGGGAGG TGAAATGTCC TTTAGTTTCT 840 TTCAGATCAT AACCAAGATG CTTAGAGGTC TCGGCTGGGG TGACTTGGCA CCCTGGCCTC 900 TGCTTATGAT GAGTCGAGGT TTCTGTCTTG GGCCTTCCTC ACTTCCTAAT GCCCTGCACC 960 TCCCATGGGG CAAGAGGCTC CGGCCTCCTC TGGCAGTTGA ATCCAGATGG ATGACAAGAT 1020 GAAGGCCGCA CAGCGATGGT TCCGCCCTGG CCTGAACCCG CCAAGCGCCC CCTCCCACCC 1080 AGAGCGCGGC CTGCAGCACT 1100
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