Tag | Content |
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EnhancerAtlas ID | HS050-20222 | Organism | Homo sapiens | Tissue/cell | Fetal_stomach | Coordinate | chr14:51427860-51430340 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF1 | MA0050.2 | chr14:51427988-51428009 | AAAAAGAAAAAGAAAGAAGAA | - | 6.87 |
| | 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 |
GH14I050961 | chr14 | 51427856 | 51429506 |
| Enhancer Sequence | ATAATCCCAG TTGCTCAGGA GGTTGAGGTA CCAGAATCAC TTGAACCTGG GAGGCAGAGG 60 TTGCAATGAG CCAAGATTGC GCCACTGCAC TCCAGCCTGG GCGACAGAGC GAGACTCTGT 120 CTCAAAAAAA AAAGAAAAAG AAAGAAGAAA ACAACCAGCC TCCATTGCCA GATGCTATCT 180 GCACAAAGAT GAATTACTGC ACAGAAAAAT TTAGTTCCAC ATTATCTCAG TCATCTCTGC 240 TGAGCTGGGC TGGAGTTTTC CTTTTGCATA ATCAGAGGTT CCATTAAAAC ATTTTAAAAA 300 CAAAAGCAGG CAGGGAGAAG AAAATAAGCA GTTTTTTTTC TGAAAACACC CTTCTGGTGT 360 TCTCAATGCA GCAATGGCTG GAACTTAAAA ATTCCCATCC TTCTAGCCAT TTTACTCTCA 420 ACTCCCCTCT TTTGTTCTGC TACACCGAGA AGCATAATTT TTGTCCTCAA GAATGTGAGC 480 AAAATGCCCT GAACATGGCT GACCTTTGAA GATCTTGCAT TTCAGCCCTC AGATGCAGCA 540 GGCACGGTGT ATCCACTTCC TCCAGCCATG GTGTCACGGA GAGGGACAGT CTTCACTGGA 600 TATGAAAAGA GAAGGCAGGG TGCCCTCTTG GCTGCAACAG ATATTCTCAT AGCTGCCTGG 660 GTATTATTTT GTGCAGGTCT ACATTTCTGA GCTGGCTGCT GATACTGGAG TGACCCAAGC 720 TCCCTTTTCT CTCCTTCCCA GGTGACCATG CTTCTCTGTC CCAGAGGGTG CAGCCTGTTT 780 ATTTCAACAA ATTCCCTTTG CACACAGTTC TGTTTTGCAG TCCAGTCTCC TTTATGCTGA 840 CATTGATCTA AATGCTTTTT AGGCACTAGT AGGGACATAA GTGACTTTAT TTTAAATGCT 900 AATCTGCTGA CTAACCCCAA GTCTGGGAAT GCCTCCAAAA TGTCTAGGTG ATGTATTACT 960 GTTTATGTAG GAACAGTTAT TCATTGTAAG TTTCCCTCAA AACAACCCTT GATAATGTTG 1020 TAGAAATCAT AGGCTGTGAT GCTTATAGCC ACCTACATAT TCCTTCCAGA GTATAGATAC 1080 TTTTTCCTCA AGATACACAT CCTGGGTCTG GGCGATTGCA GTGCAGAGAT TTACCTGTCT 1140 TGTAGCCAGC TGCCTAAGAC CAAGCTTCTG TTTGTAAGTT CCCCCCAATA AATCAATTTA 1200 TTTTATTTTT ATTTTTTGAG ACAGAGTCTC ACTTCATCAC CCAGGCTGGA GAGCAGTGGT 1260 GCGATCTCAG CTCACTGCCA CCTCCGCCTC CTAGGTTCAA GCAATTCTCC TGCTTCAGCC 1320 TTCTGAGTAG CTGGGACTAC AGGCACATGC CATCATGCCC GGCTAATTTT TTTATCTTTA 1380 TAGAGATGGG GTTTCCCCAT GTTGGCCATG CTGGTCTCAA ACTCCTGACC TCAAGTGATC 1440 TGCCCACCTC GGCCTCCCAA AGTGCTGGAT TACAGGCATG AGCCACCATA CCCAGCCCCC 1500 AATAAATCAC TTTATATCAA CAGACTGAAT TTGTCTGCCT CATTCTTTGG TGTCTTGGCT 1560 CCTTTGGCAT TTGGGGTCCA CTTTGCATTT ATGACCCTTT CATGTATGCC CTGTCAAGTG 1620 GTTGACAGGA TTTCTAATGC TATTGAAACT TCTAAATTTT AAGAAGCTCA AATGGGTTTC 1680 TTAGTGGGAA GTTGTAAGAA ATTGTATTAG AGATTATTAC CTTGATCAGC AATGGCCTGA 1740 ACATTGAAGA CTGGGAGATT TAATTGAGGA AACAGAAAAG AGATTGAGCT GAGGATGGCT 1800 CTGGAGGCAT GGGGTAAGCT GCAGTATCGG AAGCTTTCCA CACTTCGGAT ACTGTATTCC 1860 TGGTGAGAAT TTTCGGGCAC AGAAAGTAAA GTGAGGGGGT GCCAGAGAGG CACCTGGCTT 1920 ACTTGAGAGC TTTGCCTGAG GTTGGCCTTG TTCACTGTCC TCCAGGACAC TTGGTGGGGA 1980 CTAAGACCCT ACTCAGAAGA GTCTCTTTTA TACCATCTTG GTGATCCTCT GGGAGGGCCA 2040 GGGCCAGCTT GCAGGGAGAC CAGTTCTCTA TCAAAATTTC TTCAGGTCCT GGACATAAAC 2100 CATTTCAATC TATTCCAGCA AATGGGGGAG AAAGACTGAC TTCCCTCTCC TCCAAAGCCA 2160 CTCTTTGATC CCAGTTGATA ACATCTTCTT TAAGCCATAC ATGCCAGTGT AGTGAGCAGA 2220 TGGAGCTGAG AAGCATTGCT CAGTATTTAG TATTAGAGGT GTGTGCATGG GCAGTTGTGG 2280 TTGGTTTGTT CACGTGCACA TGGAACAGCT TACAGGGAAC AATAGGTGCA TGGAGTCATA 2340 TTGAAGAAGA CATGGTCTCT GCCTCCAGGT AATGCATATT CACATAAATT ACTGCTAAAC 2400 ACAATTTAAA ACTTGAAAAT CATTCAAATC TATGTTTGAG GACCCACAAA ATACACACAA 2460 AACTGGAATT TTAATTTGTT 2480
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