Tag | Content |
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EnhancerAtlas ID | HS050-12278 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr11:61541640-61543520 |
Target genes | Number: 13 | Name | Ensembl ID |
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SNPs | Number: 2 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr11:61542169-61542187 | CCTGCCTCCCTGCCTCCC | - | 6.07 | EWSR1-FLI1 | MA0149.1 | chr11:61542173-61542191 | CCTCCCTGCCTCCCTTTC | - | 6.29 | KLF4 | MA0039.3 | chr11:61543324-61543335 | GGAGGGTGTGG | - | 6.32 | Nr2f6(var.2) | MA0728.1 | chr11:61541774-61541789 | GAGGTCAGGAGTTCA | + | 6.22 | RREB1 | MA0073.1 | chr11:61543248-61543268 | GGGGTGTGGGTGTTTGGGGA | - | 7.37 |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_06236 | chr11:61535335-61561222 | Brain_Hippocampus_Middle | SE_31437 | chr11:61527611-61541868 | Gastric | SE_31437 | chr11:61541871-61545597 | Gastric |
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| Number: 1 | ID | Chromosome | Start | End |
GH11I061774 | chr11 | 61542163 | 61545499 |
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Enhancer Sequence | TTGGGGCTCA GCAAGGAAGG GAGGGCAGGA GGGCCCTTTG GGGGCACTGA AAGACCCCAG 60 AAAAAGCAAG CGTTGGCTGG ATGCTGTGGC TCACGCCTGT AATCCCAGCA CTTTGGGAGT 120 CAGGCAGATC ACTTGAGGTC AGGAGTTCAA GACCAGCCTG GCCAACATGG TGAAACCCTA 180 TCTATACTAA AAATACAAAA ATTAGCCAGG CGTGGTAGTA CGGGCCTGTA ATCTCAGCTA 240 CTTGGGAAGC TGAGGCAGGC AGGAAAATCC TTTGAACCCG GGAGGCGGAG GTTGTAGGGG 300 GCTGAGATCA CGCCACTGCA CTCCAGCCTG GCAACAGAGC GGGACTTCAT CTCAAAAAAA 360 AAAAAGAAAA AAAAAAAAGC AAGCATCTGT GTGCGTGTGT GTGTGTATGT GTGTGTAAAC 420 TCCCCCACTG CTACTGCCAC CCCGCCCTCC CGCCTTTTAT CCCTGTGCCT GCCCCTCAGC 480 CTGCCTCCCC CTCGCCCTGC GCCTGCCTCC CTCTTGTTGG GCTCATCAAC CTGCCTCCCT 540 GCCTCCCTTT CGCCCTGTGC CTGCCCCTTA AACGTTAGAC TCCTCAGCCT GCTTCCCTCT 600 CGTTGGGCAC CTTACCCTGA CTCTGTGCCT CCTTGCCTCC CTGCCTCCCT CTCGCCCCGT 660 TTCCTGCTCC AGCCTGTGAT TCCCAAGTCT GCAACCCCAG TCAAGACCCA TCTCCTGGGC 720 CCTCTACCAG GTGCCTCAGC TCCAGGTCCC AAACTAAACT CCCTGCACAC TTGCCTCCCA 780 CCCTGGGCTC CCCTCTCAGG GAATGGGGCG CAGGGCCTTG GTTACCTGAG CCGCAAATCT 840 GGGTCAGGGC CCTCTTTCCC CAACCTCATC ATGCATCTGG CCTTGCTATT GCCCTGGAAG 900 ATCCCTCTAC CTGGTCCGGT CCTCGCCTCT TTCCTGTCCA TCCCCTGGTC TGGGTTACCT 960 CCCTTCCTTG TCGGAATGTC CACAGCAGCT GGGACCCCCA ACTCCTGCCC CACTTGAGAC 1020 TCAGGGGGCC ACAGCACTCC CTATCCTTCC AAGGCCCCCA GTGTCCTCCC AGCAAAGCCC 1080 CGGCTTCCAA GCTGCACCAC GGGGGCCTTG GGGGCCCTGC CCTCCGCTCC AGCTCTGCCA 1140 CTTGTGGTAC CATCGCAGCC CCCGCCCTCC ACCCTGTGGC TCCCTTTGCC TTGGATGCCC 1200 TTCCCAACAC CCATCCCTCC TCTCCAGGCA GACTCCATGC TGGTCCCCTC CCCAGGGGCC 1260 CCTCCCCTAA GACCCATTGG GAGGCACCAC AGCACAACCC CAGTAGTGGC TGATTTTGAG 1320 TCTATGAGCT CCCTGTGGGC ATGGCTGGGT CTGTCGGCTT CGGTGTGATG AGTGAGCCAG 1380 GCATGGTACC TTGGCATGGC TCTGCCAGTG CACGTGGAGG AGTAGAGGAG ACGTGGGTAT 1440 GGAGAGGATC TGGGGAGTGA GTGGGCCTAG GTGCAAGTGG ATGGGCTTGG AGGCTGCTGT 1500 GAGGTGTGTG GGTATGGACA TGAGGGAGGG TGGGGCTGTG AGTGTGTGTG TGTGTCTGTG 1560 TGTGAGTGCA TACATGCAGA GGTGGGGGGA GCGTGTGGGT GTGGAATGGG GGTGTGGGTG 1620 TTTGGGGAGT GACTGCATGC GTAGCTGTGC AGAAGTTGGG GGAGTGGTAT GCTGTGAGGG 1680 GTGAGGAGGG TGTGGGTGTG AAGTAGGGTG TGGGGGGGTG TGACCATGCA GAAGGCATCT 1740 GAGCTTGTGG GAATCGCGGC TGAGGGCTGG GTGCTGCCCT GTTTCCTGGT GAGCTCTAGT 1800 TGGGCCAGGC CTGGCTGAGA GGGGGCAGGA GGGCAGGACC AGCCGGGTAG CCCCATCCTG 1860 AGGTGCCACT GGCTTCACTC 1880
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