Tag | Content |
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EnhancerAtlas ID | HS050-05952 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr1:221630990-221632420 |
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) |
FOXA1 | MA0148.4 | chr1:221631439-221631455 | CCTAAAGTAAACAACT | + | 6.16 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_56663 | chr1:221631167-221632605 | u87 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I221457 | chr1 | 221630771 | 221633231 |
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Enhancer Sequence | ATTTTACTTT TGGGAAAAAC TTTCATGTCA AAGCAATGAG GGGTATGTGC ATGTGTGTGT 60 GTGTGTGTGT GTGTGTGTGT GTGCATATGT GTGTGTAAGC ATCTCACTTA ACTCCCTTTG 120 GGCCCATCCC TTCTCCCTGT GTATTCCGAG TATTGATAAG AGCAGAATAT GTAAGTTGCT 180 GCTGAGGAGG CCTTGAAGAG GCAGTATGCA AAGTCACTTA GAAGCAGAAC CTAAGCCATG 240 GTTGAGTCAG ACTACTCACA TTGGCTAAAT TGTGAAGATT TTCTTCTTAT GTGGTGAGTC 300 TTCCTAATGA GAAGCTTAAG AAATAAAGTT TATTTTGTTT ATAAATGTTT CCACTTGATG 360 TGTTTTTCTC CTAAAAACAA AATACGATAA AAGCAATTTT CATGATATGT CTTTCAAAAT 420 TGAATTGCTG GTAGCATTTT TTCCCCATTC CTAAAGTAAA CAACTTCCTT TCAGATCTAA 480 AATGTAAATC ATAATTGTGC TTTCTTTCTG GGGCTTCTGC CTTTTGTCAA ATTAACAGCT 540 CTCGAAAGAA GCGCATATGT TCAGCTGACC TGCAGTTGGA CCTAACATTT CTTTCCCAAA 600 CTGTCAGATA TTTTAGTCAT GGAGGAGAGA GGACACACTT CCAGAATCTG CTGTGTGTGG 660 CCCGGATCCT GTTCTCTGGC CCCAAGCAGT CTAATCGCTC TGCCTCACAG GGGCCGCTTT 720 TGGCTAATGA ATCCTTAGCT CCAAGTTTTT CCTCTTCCTA ATGAGTGCTA ATAAAATGCA 780 TTTAACTCCA CTAATGCAAC AAAAACTCAG CATTATTTCA TTGTATCTAC TTAATAAGAA 840 CCTTGTTTAA TATCAAATTA CAGCCTGTTC AGCCAAAGCA TTATACAGGG GGAAGTGGGA 900 CTGTGAGAAG GGAGTATCAA GTGCTCTAAT TTAGACATTC CTCCTTAGTA TGCCCTGCAG 960 TATTACGTGA TTGCTTAATT CATTTAGCCG AGCTAGTCTG ATCCATCTGC CAACTGTTGT 1020 GTAAAATTTA CTGCAATGCT AGGCAACCAG TCCCACCACA CAAGCTAGAA ATATAGTATC 1080 GCTTTTCCTG GGACCAAGTT ATTAACAGTT GTTTGGGGAG AGGCAAGAGG CAATGGTGCA 1140 GATACTGTTA CAAAAAGGAA GACCTTCTGG ATGTGCCTCA TTTTATAAAA TGGTTACAGC 1200 AAATCCCATT TTTTATTCAT CAAAATGTGT TTCTAATTGT TCATGGTCTA ATTTCAGAGG 1260 CATTTCATCT TTACTTCAAA TTTATCTTCG ATGAGCAATG ATGTCTAATT TCCTATTTAT 1320 CTTAGCTTTG AACTTCTCTG TCTTCTTTTG ACCAGCCTCT CTCTCAAGAA ATGATCAGTA 1380 ACGAACATCT ACTGGAAACT TTCCATGTGA AGGAAAGAAT CATTTTGTAA 1430
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