Tag | Content |
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EnhancerAtlas ID | HS050-01161 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr1:24053680-24055960 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ELF3 | MA0640.1 | chr1:24054778-24054791 | AACCAGGAAGTGA | + | 6 | HSF1 | MA0486.2 | chr1:24055833-24055846 | GAAGGTTCCAGAA | - | 6.33 | IRF1 | MA0050.2 | chr1:24054845-24054866 | TCTTTCTTTCTTTTTTTTTTT | + | 6.25 | RARA | MA0729.1 | chr1:24055067-24055085 | CCTCGAACTTCTGACCTC | - | 6.64 | ZNF263 | MA0528.1 | chr1:24055567-24055588 | ATTCCTTCCTCCTCCTCCTTC | - | 7.24 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 24055576 | 24055887 | chr1 | 24054400 | 24054827 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I023726 | chr1 | 24053079 | 24056171 |
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Enhancer Sequence | TGATAGCATC AACCCTGTAG GGTTTTAAGG ATTTGGGATA ATAGGATGTC AGTATCTCAC 60 TGAAGAAACT GTCCCTGGCC GTAGTTCCTG GCTCCATTGC AGAGTTGGTA ATACCAGTCT 120 CTGAATTTTC TTCCTGAGAG TGGATCCCAT TAAATCTCTA GCCAAGGAGG AGCGTACTTC 180 TGTGCTTCTA GGGCTAGACA GAACGGAAGA TGGTGCAGCA GCCCCAGCGT GGGAGGCCGG 240 GGCTGTAGTG GGGATGTGGT GAAAGACGTA GGGCTCTCTC TGTTGCTCTC AGCTGCAGCC 300 ACGTGTTGCC CCATGGAGAC TGGGCCAGGA GCTGCTGGAT CTTACTGTTT CTCAAGAGAA 360 GTTGTGAAAT CTCCTCATTT TAAACTCTTG GCAATTATTT CATTTTTGTA AACATTGGGA 420 GAGCAAACAA AACATGTCGG TAGGCTGTAT TTAGCCCACA AGCTGCCAGT TTGCTATCTA 480 TGTTCTAGGC TTTCTGTGCT TGACTTAGCA AAATATTTAC TAAGCGCCTG CTGTACCTGT 540 AGCTCCTCAG TACCTGGTCA TGTTTACTGT TCTGCCACCT CAGGCGTGCT GGCTCAGTCA 600 TCCTATCAGG TACTAAATCA GTTTAGTGGG CTTGAAATGG TGTTTCAATT CAAATTAAAA 660 TGCAATTTGC ATTTCCCTGA TTACTGCTGA GATTGAACAT TTAAAAAAAA TACATCTATA 720 GAACTTTCTT CTCCCTCAGT AGAATTTTTG TTTTAAGTCT TCAGATCATC CTTTAGGTAT 780 GGAGAGATTT AGGGCTTCCC TAGTGAAATA TTTCTTTTGA ATAACATCAC ATCCACTAGC 840 CTGGACTCTT GTTTAGGTTT GGGGCTGTCT GCACATCTCA GGAGGCCAAG CATCAAGCCC 900 AGTACCGCCA CAGAGGGGGG GTTCAATAAA TATTTGAATG AATCTTTATT CCTATTTCAA 960 GAGCGTATTT CTTCTTTATT CTCTAGTTCT TGGCACAAGT ATTATTGATT TAGTTATCAG 1020 CGTATTCAAC AATCACAACT CCCCACTTTG GTGAGGAAAC ACACTTTCTA GAGGTTTGCC 1080 TGTGTCCTGC CCCATTCAAA CCAGGAAGTG AAAGGGGAAT CTGCTGGCCT TAAGGGAACA 1140 ATGATTCTTT TTTCTTTTCT TTCTTTCTTT CTTTCTTTTT TTTTTTTTTG AGATGGAGTC 1200 TTGCTCTGTT GCCTAGGCTA GAGTGCAGTG GGGCAATCTC AGCTCACTGC AATCTCCGCC 1260 TCCCAGGTTC AAGTAATTAT CCTGCCTCAG CTTCCCGAGT AGCTGGAATT AGAGGTGCCT 1320 GTTACCACGC CCAGCTAATT TTTGTATTTT TAGTAGAGAC GGGGTTTCAC CATGTTGGCC 1380 AGGCTGGCCT CGAACTTCTG ACCTCAGGTG ATCCACCCAC CTCAGCCTCC CAAAGTGCTG 1440 GGATGACAGG CGTGAGTCAC CGCGCCCGGC CTACAGTGAC TTCTCTAGAG AGTAGTTCCT 1500 TGAGGGCTGC AGAAGGTCAT GCTAGTTTGA ACATAGTGGT TCCATGTGGC TGGTTTTACA 1560 TCTGTGCTCA GATGATTTGT TTTTTTTTTG TTTTTTTGTT TTTGTCTTCA AGGTAGAAGA 1620 ACACTCTAGT CCCACAGGCC CTTTAATCAG TACCCACTGG GGAGTATTTG TGGATGTGTT 1680 TATCAGTTTC AGGGTGTCTT GACCAAGATT CAGGAGGGAG GGTATCCCCT ATGAAGATGG 1740 CCTTTTTCTC TTGGCTCTCC TTCATGCACC CTTCTCAAGC CGTGCTTACA TTTCCTCTAA 1800 CACTGCAGGC TCCATTGGAA CTCCAGCCCC TTTACACCTG CTGTCACCTC AACTGGAGTA 1860 TCCTTCCACT CACTTATCAT CTGGCAAATT CCTTCCTCCT CCTCCTTCAA GATCTAGGTC 1920 AGATGGTCCC TTTCTGAAAC CTTCTGTGGC TCTCCCGGCA GAGTTAGGCC TCCCTTCTTT 1980 GTAGATATTC ATTAACTCAC ATATTTGGTT AGCTACCAAA AAATCGTCCT TGCCCTAGAG 2040 GAGTTCATAG GCTAGTGGGG TAGACAAACC TAAACATTTA GACAGCCATG CTGACTGCAT 2100 TAGGGAAGCA CTGAGGAGGA GCACTTCACC TGCCTTGGGG GACAGATGAC AGGGAAGGTT 2160 CCAGAAGGTG GGGACACCTG AATCCTAAGA GTGTGTGGGT ATCCAGATAA GGAACTGGCT 2220 TGGGCAAAGG CACAGAGGCA ACAAATAATG TTGCAGGTGC ACAACAATGA CAAGCAGTTG 2280
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