Tag | Content |
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EnhancerAtlas ID | HS134-01682 |
Organism | Homo sapiens |
Tissue/cell | Mesendoderm |
Coordinate | chr1:62802770-62804200 |
Target genes | |
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) |
EWSR1-FLI1 | MA0149.1 | chr1:62803502-62803520 | GAAAGGGAGGGAGGGAGG | + | 6.13 | NFYA | MA0060.3 | chr1:62803790-62803801 | TCTGATTGGCC | - | 6.02 | NFYB | MA0502.1 | chr1:62803791-62803806 | CTGATTGGCCCGGCT | - | 6.16 | SOX10 | MA0442.2 | chr1:62803136-62803147 | AAAACAAAGAC | + | 6.14 | ZNF263 | MA0528.1 | chr1:62803504-62803525 | AAGGGAGGGAGGGAGGGAGAG | + | 6.58 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I062336 | chr1 | 62802093 | 62804728 |
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Enhancer Sequence | GAAATGGACA TTCTCCTATT AATAAGCCTG GCTAAGTAAG GCTGATCTGC AGCCAGGGTG 60 AATCTGAAAG CCTCCTTCCC CACAGAGTCC CCAAGGGCAA CAGACAGAGG GGCGTGCTCT 120 TGTCGATGGA CAGGCCCACA CTGGTCATTT CGGGCAGGAA ATTCTGTAGG GGAAGAGATT 180 CCTCAACCTC TTATGCCTGC TCTTGCCCTT CTTGGAGGAG CTCAAAAGCA GAATTTCTGT 240 GGCTGAAAGG AGGATTTCCC CAGGGCCAGG CGTTGCCTCT CCCAGGCTCC GCACTGACAC 300 TCCTGGACAC TCCCACAGCC TAAGGAAGGA GGGTCTATTC TTATTCCCTC CTTCCTTATA 360 GATGTGAAAA CAAAGACAGG GGAGAGTTCA TTCTTCTCCA AGTTCTCACA GTTAGAAAGG 420 GAAGCTGGGA ATTGAGAGGG TTGCAAGTCA CCACTCCCCA CCGTGCCTGC CCTCCTGAGG 480 CACGGTTTAG ATGCTGCCCA GGCCTTCGAA GCCAACTTCT TGCTTTGCCT GGGCAGTGGT 540 GGGAGGCGGC TGCTCATCAC CGCTGGGCTC TCCCTTTCTT GCTCACTTGG CTCTTTGGTG 600 TCCTTGTCAT AACTGAAAAA GCCATCATGG GCTGACGACC AGGTCCCCTT CACCCCAGAA 660 CCATTTTGTG GGAGTGGTCA CTGCCCGGCT CCCCTCCCCT CCTGTGTCAT CAGACACTCA 720 GTCACCCAAA GAGAAAGGGA GGGAGGGAGG GAGAGCCTGG GGCAGGGGCA GAGGCGCCTC 780 AGCCTGACAT CATGGCTTCT GTCTGTGTCA CTGCCTTTCT CCTGCCTTTC CCAGTCTGAC 840 TTCTCACTGT AAGGCTTCTA CTAGCCAGTT CTCTGCTTCC CCCATCTCTC TCTTCCTCAT 900 AGGCCCCCCA GCTCTAGCTC CACCATCTGG AATCTTCCGA GGAGTTCCTG TGGCCTCCAG 960 TCCCGCAGCG GACAGACTGC ATGTCTCAGC ATTTCTTGGT TCAAATTCCT GAGGCAGGAA 1020 TCTGATTGGC CCGGCTCCCT TTTCGTGCTG GGCCACAGGT CATAGGTTGC TGGCCAGCCT 1080 CAGTTGGCTG TCCACGGACA GCCAGAGTTG AGTGGGACAA AACACAGCTG AGGAATGTCC 1140 CCTCCTTTCA GCCGAGGCTG TTTGTTGAAT TGTTCCTTTT AGAAGGGACA ATGGCCAACA 1200 TTTGTACTGT GCTTCTAAAG CCTCTGCTGG CCTGAGGCAG GAACACAGTC TTTTGGGTCC 1260 TTTATAAATA ACTGTTTTAA CTGCTAGAAC AACTTACAAT ACGAAGGCTC TCACTCCAGC 1320 TTTCACTACG GCGTACCCCA TCTCTTTCAG ACTCCTCTCC TTGCCCCAAA TCTGTCCCTG 1380 GGAGCCCCCA GTGGTGACTC AGGGGTGAGT CCAGTCTGCA GCCGACTGCC 1430
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