Tag | Content |
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EnhancerAtlas ID | HS177-03608 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH_RA |
Coordinate | chr10:133775150-133776570 |
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) |
IRF1 | MA0050.2 | chr10:133775941-133775962 | TTCCGTTTTCATTTTCCTTTT | + | 6.3 | Nr2f6(var.2) | MA0728.1 | chr10:133776450-133776465 | GAGGTCAGGAGTTCA | + | 6.22 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_47883 | chr10:133776060-133776372 | Pancreas |
|
| Number: 1 | ID | Chromosome | Start | End |
GH10I131961 | chr10 | 133774987 | 133776470 |
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Enhancer Sequence | CGGCACCCCC GAAGCTGTGA CAGGTGCAGA GGCGCTGCCG TCCTGGGCCG GGCCTCACCT 60 TCCGCCTTGT GTGCTCTGGC GCCAGCACCC AGTCCCAAGG GCACAGCGGC TGCGACTTGC 120 CTCTGGCCAG GGCAGGTGGT GGTGTCATAC CCAGGACGGG AACCCACACT TGATGTCCTC 180 CAGGGTTTTT TTTTTTTACA TTATCTTAAG GACTGACAGT CTCCCACCCC ATCTGCTCCC 240 ATCTGTCCCT AATTTCATGC GCCTCCGCCT GAGTTCCTGC ACGCATTTCC TGAATAAACA 300 CACCCCTGTG CCAGTCAGAA CCCGCGGGGG TTTTGGAAGT GAGAGCCCAG CAAGGCAGCT 360 GGCCAGGGGG CGGCACTGCC CTCCGGGGAG CACCGGTGCC CGGGACTCTG CTTCTGAGGC 420 TGGCCTGTAC GATGATTTTG TATAAATATC TCCAATCAGA ACCTTTTTAG TGTATTTCTT 480 AATATAACAG AAACTGGTGT CTTAAAATAC AAGACTAGCT GCCCGGTGAT GACACCAAAT 540 CGAGCAGCGG GGCTCGCAGT GGCCAGGATC CCCGACAGTG GAATGCTGAG GTTAGAACTG 600 AAACCGCGTT TCGTGAAGTC ATCATCACGC ACGGGAAACA GGTTTGGGGT GAGGGGCGGT 660 CCAGTCCTAA GAAAGCTCTC CAGCTCCACG CGGTCACCTT CACTCACTCA CCAGATGCAG 720 ATTGCAAAGA GGCGAAACCT GTGATTTCTT TAATAATCAC AGTCTCCATC TGGTGAGTGG 780 TTAAAGTCAC GTTCCGTTTT CATTTTCCTT TTGGTGGCTG GGAAATGCTT CTGATAGTAA 840 TAGTTTTCGA TTCTGCAACT CCCATTGTCT TAGGCTCTGT AGCTCTCCAT TTTCTTCTTA 900 TCCTTGGGAC GTGTCTTGGA CGTTTCTAAC AGGCTGTGTT CCTGGACCTG AAACTCAGCT 960 GGAGACTGGG TCCCTTGCAG ATTTGCAGGG ACCGTCCATC GCTGGTGTGT AGATGCAAAA 1020 ACAAAACACT GGCACCACCC AGTCAGAACT GGCAGGGGCT GCCTGCACTG GGCACCAACC 1080 CCGCAGATGG CCAGGCCCAG ACCACGTGAC TGCCTGCTGG GCTCCACCCC CAACCGCAGC 1140 CCAGCCAAGG CAGAGAGGTG GCTGCACTTC CGCCGATCAG AGGTCCAGAT AGAGCTCCGT 1200 CTGCTTGCCT TGGAGTTGTT AGAAAATTAT CTTTGGGGCT AGGCATGGTG GCTCACGCCT 1260 GTAATCCCAG CACTTTGGGA AGCTGAGGTG GGCGGATCAC GAGGTCAGGA GTTCAAGACC 1320 AGCCTGGCCA TCATAGTGAA ACCCCGTCTC TACTAAAAAT ACAAAAAATT TAGCCAGATG 1380 TGGTGGCGGA CGCTTGTAAT CCCGGCTACT TGGGAGGCTG 1420
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