Tag | Content |
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EnhancerAtlas ID | HS003-06468 |
Organism | Homo sapiens |
Tissue/cell | A549 |
Coordinate | chr10:103989400-103989940 |
Target genes | Number: 13 | 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) |
CTCF | MA0139.1 | chr10:103989685-103989704 | AGACCACGAGGTGGCGCCG | + | 6.44 | SNAI2 | MA0745.2 | chr10:103989573-103989583 | AACAGGTGCA | + | 6.02 | ZNF263 | MA0528.1 | chr10:103989894-103989915 | GGAGGATGAAGGGAAGAGGAC | + | 6.17 | ZNF263 | MA0528.1 | chr10:103989891-103989912 | GGGGGAGGATGAAGGGAAGAG | + | 6.74 |
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| Number: 1 | ID | Chromosome | Start | End |
GH10I102229 | chr10 | 103989392 | 103992010 |
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Enhancer Sequence | TGCTACCAAG GGGATGATCT GCAGGTGGGA CGCCTGAGGG TGTGTGGAAG GGTGAGAGGC 60 ACACACACAG ACACTGAAAG AATCCTAGGC CTGGTAGGCA CTTAACAAAT GTCTGTTACA 120 GACCAGAATT TTATTGCTGT TAGAGACCCA AGCCCCTCAT AGGAACAGTG AGAAACAGGT 180 GCAGAAAGGC GGAGTAACTT TATCTAAAGT CATAGGCTCC CTGAATAGCA GAGCTGACAC 240 CTACAAGGAA GCGTTGGAGA CCAGATCTAC CAGCTAGCCT CCCTGAGACC ACGAGGTGGC 300 GCCGCAGCAC CGGCTGTGGC CGATGCCAGC CAGGTAGCCG GTTTCCCACG TCCCCCGCAC 360 GCACGCACCT CTTTGCTGCA GGAATCCCGG GCTGCCCCGA CCTGGAGTAG GGGGGGTGGT 420 GAGTGGGACT GAGTCCCTAG AAGCCTGGAC CCTCACTTCG TTCCTGTACA TCCAGCTCGC 480 CTGTAGACAG TGGGGGAGGA TGAAGGGAAG AGGACTCAAG CGCAACTTTG AATCATCACG 540
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