Tag | Content |
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EnhancerAtlas ID | HS101-05968 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr10:102852010-102854160 |
Target genes | Number: 10 | Name | Ensembl ID |
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SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF1 | MA0050.2 | chr10:102852034-102852055 | TCTTTCTTTCTTTTTTCTTTT | + | 6.11 | RREB1 | MA0073.1 | chr10:102853548-102853568 | CACCCACCCACCCACACAGG | + | 6.38 | ZNF263 | MA0528.1 | chr10:102853833-102853854 | CTTCCCTTCTCCCTTTCCTTC | - | 6.03 | ZNF263 | MA0528.1 | chr10:102854098-102854119 | GAAGGAGGAGGAGGAAGACAA | + | 6.86 | ZNF263 | MA0528.1 | chr10:102854104-102854125 | GGAGGAGGAAGACAAGAAAGG | + | 7.15 | ZNF263 | MA0528.1 | chr10:102854095-102854116 | AGAGAAGGAGGAGGAGGAAGA | + | 7.85 |
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Enhancer Sequence | TTTTTTTTCT TTTTTCGTTT TCTTTCTTTC TTTCTTTTTT CTTTTTTTTG AGACAGGGTA 60 TCACTCCATC ACCTAGGGTG GAGTGCAGTG GCGTGATTAT GGCTTACAGC AGTCTCAAAT 120 TCCAGGGCTC AGGCAATCCT CCCACCTTAG CCTCCCGAGT AGATGGGACC ACACGTGTGT 180 ACCACCAAAA CCAGCTAACT TTTACATTTT TTGTAGAGAT GGGGGTCTCC CTATGTTGCC 240 CAGGATGGTG TCAAACTCCC AGGCTCAAGC AAGCCTTCTG CCTCGGGCTC CCAAAGTGCT 300 GGGATTACAG GTGTGAGCCA CTGCGCCCAG CCTACATTGT TTTCTTGGAT GGCTGTATGA 360 TATTCCATCA TATGGCTACG TTTTAATCAT GTTGCTTGTG CCCCAGATGG AAACCTAGAC 420 TGTTTCTAGT CTTTAGCTCT TACAGTACTG CAAAAATACC TTGATATATT TCTCTGAGCA 480 CAAGTGCAGG ACATATATAG ACAAATTCCT CGAAGCGGAA TTGTTGGGTC AACTGACATG 540 TTCATTGAAC ATTTTTGATA GATATTGCCA GACTGCACAT GAAGATGATT GCACTGTCTA 600 CCCCCGGTGT CAAACCGGCA GAGGGGCTGC CTCCCAGGTG CTCAGCTCAG CCACCTCAGT 660 TGCTCTCAGA CACACTCCTG GACAGCTCCC GGGATGGGGG AGTCCCAAGG AGAGCACGCA 720 GGACAGGGAG CGCAGCTTCC CCTGGGAGGG GTGGGACAGG AGGGACAGGA GCCAGCCCTC 780 CCCTCTAAGC CTGAGAAAGC CACTAGGTAA ACTCGGTTGT CAGAAGGGAG GGAGAGTTTC 840 AGTCAGGGTC AGGGGTTAAT GCGATGGAGC TACTGGGACA CACTGTGCAA ACAAAACAAG 900 TTAGGGGAGG GGAGGGGCCG GCCCTCTGGC CACAGGGAGG GAGATGGGCC AGTCAGCCTG 960 CACTTGGCTC TTCCCTGGGT AGCTGCCATC GTGGGCACAG GTTCTGGGCT GTTGAGGACC 1020 TTGTGGCCAG GCTGCTGGGC TCTAAGGCCA AGAGGGCAGC ATTCTCCTTC TGAAGGCCGC 1080 CCCCCAGAGC TGGCACGGTA GGCCTGCTGA GCTGCCTTGC CCACCTTCAG GGCCCCTCCA 1140 CAGGTAATCC CCCTGGAGCC CTGTCTGGGA GGCTTTGGAC GGTATTAGAG GTGAGCCGGG 1200 TGGCAGGCCC TGGAGCCAGG CCCAGCTTTT AGAGCATTCC TGAGCATTAG GCTCCCTGTC 1260 CCAGCCCAGC CTTGCCCTCA CCCCATGGAG CCCCTGGGGC TTCTCTGCTT CAGCTGCTGC 1320 TGGCCTAATT ACAGGTGTCC ATGTCAGGGT CAGCAGTGGA GTTAATTCGG GGCTTGTCTT 1380 GGGGTGGCCG GGGCTCATTA ATGGAGTCCC AAAGAGCCTA GGGATGAGCC AGGCAAACAG 1440 GGGATTAGGG GCTGAGGAAG ACTGCTGTGG GGGAAGGCTG GCTAGGCAGG GCTGTGAGCT 1500 GGGCCCCGGG GAGGGGGTCA GCTTCAAGCC TGTGTGTTCA CCCACCCACC CACACAGGCC 1560 CTCATGAGAC CCAGCAGTGC TCAGACACGC AGACACACAC AGCCACGGGC CAGACACTCT 1620 TCAGAGACAC ATATGGACTC TCATACACAG GCTCACACAC ACAGACACAC ACCATTGGAC 1680 TTAGAACTGC TCCCTGAGAA GCCTTGAGGT GTGCAGGAGG GGTGGGGGAG ATGAACCAGA 1740 GATTTCCCTC TTCAGCCAGA AACTCTGGCC TGCCCCTGCC AGCCCCCTCC TGTGCCCTCT 1800 CCCACCCTGG CCAGGGCATT GAGCTTCCCT TCTCCCTTTC CTTCAGCATG TCCTCCCACC 1860 ATGGACTGGA ATTCCGAAGC ACTGGTCTGT GGGTAGAATG AAAGAGCCGG CTCCCAGCCA 1920 GGATGCAGGG AGGCGGGGGT GGTTTCTCCA CACCCCTCAG TCCAGCCTGG CCTAGAGGGT 1980 CCCTGAGCCC AGCTGTCAGC CCACCTCCCC CATACCAACC CTGTGCCTCA TGACAGCCCT 2040 GGGGTTCTGT GGGGAGGCAG AGCCACACTG CACAGAGGTC ACCAAAGAGA AGGAGGAGGA 2100 GGAAGACAAG AAAGGAGCTG ACAGGAGCCA GGGTTGGGGC GGGGGCTGGG 2150
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