Tag | Content |
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EnhancerAtlas ID | HS052-03158 | Organism | Homo sapiens | Tissue/cell | Fibroblast_foreskin | Coordinate | chr1:200328750-200329840 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NKX2-3 | MA0672.1 | chr1:200328902-200328912 | ACCACTTGAA | + | 6.02 |
| | 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 |
GH01I200359 | chr1 | 200328729 | 200329728 |
| Enhancer Sequence | AATGGAAGTA TTTTAGCTAC AGCAATGTCA CTCAAATCTT TGAAATCCTT GAAAGTCATA 60 GCCCCAAATC ACGTTGTAAT CTATCCTTAT GTTCAGCCAG GCACAGTGGT GTGCAACTGT 120 AATCCCACAC CCTTTGAGGC TGAGGTGGGA GGACCACTTG AAGTTCCAGG CTGTAGTGTA 180 CTATGATCAC ACCTGTGAAC AGCCACTGCA CTCCAGCCTG GGCAACATGG TAAGACCCTA 240 TCTCTAAAGA GTGTGTGTGT CTGTGTGTGT GTGTGTGTGT GTGTGTGTGT GTGTGTTTAG 300 GTCTCCCTTC AAGTATGTTG AAAGCGAACA GCCAGACTCA TCTGACTTGT AAAAGGAAGT 360 GTCACTGGCC CTGAGTCATT CACATTCTCC TACATGCATT ATATTTGAAA TTGGACCTAG 420 GTTTGGGTCC CGGAGGTTTT TTTTTACCTT CCCAAACACA CCATAGGAAG ATGATGGAAG 480 TGCAAGAGGT GTGCATTTTC CCTGTTCTCT AAGGGATCCA TTTGAGAAAA GTGTGTATAT 540 ATGGACAGTG AATATCTGAA AATTGCTTCC CTCCCTCAGA ACCACTGATT CTATTTGCAG 600 CCACGTGACT CTCAAATCTA GCTCATCTCT TACTAAGACC CTGACCCTGC AGCCTGAAGC 660 ACACTGCTTC ATCAGCCCTC AGGCCCCTCA ATAGGTCTCA CATTGAGCTA ATCTTCCCCA 720 AATAGATCTC CCTTACTAGC AGGCACCCTC ATGCACTCTG TTCACCACAC TGCTGCCAGA 780 TCAACATCCT ACACAAGCAA ATCCTGTCAA GTTGCTCCTC CACTTGAACT CCTTCACTGG 840 TGCCCAGAAT CTACCTTAAC CCTTTGCAGG TAAAGCACCT CATCTGAGAA ACAGTGAAGT 900 CAGGTCCTCT ATGGGGAAAT GACACATGCT CTCAGGCTGA CCCTCTGAGA CCTGGTTAAG 960 AAGTGCCAGA CCTCAAGGAG ACAGGACAGG TTAGTGGTTA AAAGGATGGA CTCTGGAATG 1020 GAACTACCTG GGTTAAAGGC AGTTTACTCA CTGATAACTT TGACCCCCTG AGCCCATTTC 1080 TTCATCTGCA 1090
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