Tag | Content |
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EnhancerAtlas ID | HS108-17085 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr17:45053760-45055230 |
Target genes | |
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) |
Foxd3 | MA0041.1 | chr17:45053912-45053924 | AAACAAACAAAC | - | 6.32 |
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| Number: 3 | ID | Chromosome | Start | End |
GH17I046976 | chr17 | 45054121 | 45054230 | GH17I046979 | chr17 | 45054253 | 45054270 | GH17I046977 | chr17 | 45054801 | 45055010 |
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Enhancer Sequence | TAATTAGCCA GGCATGGTGG CGCGCGCCCA TAATCCCAGC TATTCCGGAG GCTGAGGCAG 60 GAGAATCGCT TGAACCTGGG AGGCAGGGGT TTCAGCGAGC CAAGATTGCG CCACTGCACT 120 CCAGCCTGGG CGACAGAGTG AGATTCCATC TCAAACAAAC AAACAAAAAA CCAAAAAAAC 180 AAATTTAACT CTTGACTCGT TCTCTTCTCG CCCCAGTCAC ATTTAGTAGC AGACCTATTT 240 TATTAGAGGA GAGTTCTCGC AGTGTTCGCC CTAACTTGGC CCGGTGGAAA AGCGTGTAAG 300 CCTGTGTTCT TTCTGAAACC ATTTTCTGGT CATTTGGGAT TTTACGCAAA TGCCTGTAGC 360 TGTCTGAGCT GCATTCCCCA AACCACTGAG GGCAGCCCAG ACTCCAGATA ACTGCACCAC 420 CTACATGACG AAGCCACTTA TCCAGGTTGC CTGAGTCACT GAAGGCTGCT GTCCCCAGAT 480 CAGGCTGGAC TTCCTGCAAG TCACACCAAA CCATCAACAG AACATTCTCC ACATTCGGGG 540 TTTTTCCCCC AGAGACACTT TACAAGGAGT GTCAGTTCCT CCCCTCACTG GCCTGGCCTG 600 AATTCTCCCA GGTCTGAGAT TGGGACGACC AGGGTTGGGG GATGGGGCAC ATCCTGATCA 660 TGATAATTCT GACCACACAG GAGCACTTGG GAGCCAGGAC GACTCTGGAT CCTTCATAGC 720 CAGGGACCAT CTGTGCCTTC GAGAAACTCC CCCACCCCAC CTGTGCCAAG CCTCTCCCTA 780 ATGAAACTAG TGCCAAATAC ACGGGATCGC ATTCCCTTCG CTTCTCTTAG CTAAAAGCAG 840 CTAAGACTTC AGTCACCTTC CTCGTTATTC TTCACTCCCA CCCACAGCAA AAGAGAGAAG 900 AAAGGGAGAA ATCCAGTCTC TCCCCGACCA AGTCTTCCAA GAACCGCTTG AGCGGGGTTG 960 GCACTAGGAC TAAGTGTAGT GGGGGATACA TAGGCCAGAA AGCCCAGCCT TCTCTCCTCC 1020 AGTGTCCCCA GGTCCCCCTG TCCCCAACTT CCAGAAAGCA GAGCTGTCCT CTCGCTGTCC 1080 GCTAGGGAGT AGCCAGTTCT TGCTGCTCCA CACTGCTGCA AGGGAAGTTA GCACCTGCAG 1140 GAGGCGTGGG TTTCTGGGCA GCTGGGGCAT CCTGTAATGG GAGGCTCCAA GTCCCCTGCA 1200 GGCAACTGCG TTTGGAGGCC ATTTTCTCCA TTGTATAATA AACATCCTGG GACTTCCTCA 1260 CCACAAAGCC GCCAACCCCC ACCCCTATGG GATGCAACAA GGGGGTTTCT TCCGTCTACT 1320 CATCTGTCCG CTATAAGGGT AGGGACAAAG CAAGCCCTTA GAAGGGGCTT TGGCCTTATA 1380 ATTAAACTTT TAACTAGATC TAGTTTTCCC CTCTGCCAAA TTGAATTTTC CTTGTTCACA 1440 TTTTCTTCGT TTTGGACACA GCTGACTGAT 1470
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