Tag | Content |
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EnhancerAtlas ID | HS108-17899 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr17:75859600-75860830 |
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) |
PRDM1 | MA0508.2 | chr17:75860220-75860230 | TCACTTTCAC | + | 6.02 | REST | MA0138.2 | chr17:75860508-75860529 | GGCAGCACCATGGCCTGGGCC | + | 6.24 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_20722 | chr17:75859212-75861867 | CD56 | SE_33705 | chr17:75859589-75863133 | H2171 |
|
| Number: 1 | ID | Chromosome | Start | End |
GH17I077863 | chr17 | 75859411 | 75862009 |
|
Enhancer Sequence | ATATGTATCA AAGCTCAAGG AACAAGTTTC CTTCTGGGGC TGCCCATGTC CCCCAAGAAT 60 GGGCTGTCCC CTGGAAGAAC CAGGGGAACA CTCATCAGTC CTCTAGACCG TCTGAATCTG 120 GTTGCTGGTG AGCCCAGAGA GGGGAAGCAA CCTGCCCCGA GACACACAGC AAGGCAGCGG 180 CAGGAGGCTC CCAAGGCTCT GAGCTCCAGC CTCTCACTCC ACCACCAGAC AAGTTTACAA 240 TGGAACTAGC TCACGCCCCA ATGACATGGA AGGGAGAATG AGCCCTTGGT AAATATGAAA 300 AGCCACCTCC TCCCTCCTGA AGTCTCCACC ACCAACAGCT GCTCATACAC TTCCTGCTAT 360 CTTCATGCTG TGGTCAAGGC TGACCTCTCT TCTCCGCCCT TCAGGAAGAG AAGACATTAA 420 AGCATGTGAG AGAGGGGAGG GCCCTGGGGA CGGGGAGCCG GCAGAGCCGC CAGCCTCGCT 480 GAGTGCAGTG ACAGAAAGCA GCCACTCCCG CCTTCAGTGT GGAGCCCAGG CCGCACCCAG 540 CCTGGAGTCC GGGGCCTCGG GCAAGCTGCC TCCCTTCCAG GCCGGCGTGG GCCACTCCAG 600 GACCCCGGGA CTCCCTGCCC TCACTTTCAC AGAGGCAGCT GGGTGTTCTG GGTGCACAGC 660 TCCTGTCAGC AGAGCAGGCT CGGGAGCCCA CTCGGCTTCA GGCAACCGTC AGCAAAAAAC 720 AGTAACAGCA CGATCCCTCC TGCTCACAGG CACCTTCCAT GCCAACAAGT CCTGCAGGAA 780 AAGCCCAGAT GACTCCAGGA TGGGCCCCTG ACTTCGAGGC AGGCCAGCCC CCTCGTTTCT 840 TCACTTTTTT GACCCATGAG GAAACAGAAG CATTCATTAG CCAGAAGCAT GTGGACGTCC 900 ATGCAGCCGG CAGCACCATG GCCTGGGCCA GCAGGGGCCG AGAACAGGAC ATCTGATTCT 960 TTCCTCACCT TCCCTCAAGG ACAAGGTCAG CCAACAGAGC ATGGGGGCGA GGATGTGATG 1020 GAAGAATGCA TTTATAACCA AGGAGAGCCA GACTGCCCTC ACCGGCTAAG ATTAGGCAAT 1080 AAAGGAGTGC TGAGGTTTGC ATAGAATCAG GGCTGCCTCC CTGGAAGAAG AGGACTGTGA 1140 ACCAGGTTGA GAAGGCCCCA GGACTGAAGC ATGTACCTAA CTTCTGGTGT TAAAATGTCT 1200 GCACAGTTCT ACCCGCCTGC TTGCTGGGCA 1230
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