Tag | Content |
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EnhancerAtlas ID | HS197-19910 |
Organism | Homo sapiens |
Tissue/cell | ZR75-30 |
Coordinate | chr7:101170730-101172440 |
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) |
Nr2f6(var.2) | MA0728.1 | chr7:101170835-101170850 | TGATCTCTTAACCTC | - | 6.32 | RREB1 | MA0073.1 | chr7:101171339-101171359 | GGGATGGGGGTGGTGTGGGG | - | 8.27 | ZNF263 | MA0528.1 | chr7:101171779-101171800 | TCCCTTCCCTCCCCTTCCCTC | - | 6.16 | ZNF263 | MA0528.1 | chr7:101171793-101171814 | TTCCCTCTCCTCCCCTCCTCT | - | 6.75 | ZNF263 | MA0528.1 | chr7:101171702-101171723 | ACCTCCTCCTCCTCTTCCCTC | - | 6.88 | ZNF263 | MA0528.1 | chr7:101171823-101171844 | TCCTCTCCCTTCCCCTCCCCT | - | 7.09 | ZNF263 | MA0528.1 | chr7:101171699-101171720 | TCCACCTCCTCCTCCTCTTCC | - | 7.32 | ZNF263 | MA0528.1 | chr7:101171788-101171809 | TCCCCTTCCCTCTCCTCCCCT | - | 7.42 | ZNF263 | MA0528.1 | chr7:101171785-101171806 | CCCTCCCCTTCCCTCTCCTCC | - | 8.35 |
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| Number: 1 | ID | Chromosome | Start | End |
GH07I101527 | chr7 | 101170976 | 101171992 |
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Enhancer Sequence | CCCGAGTAGC TTGGATTACA GGCACGCACC ACCACGTCCA GCTGATTTTT TTTTTTTTGT 60 ATTTTTAGTA GCGACGGGGT TTCACCATGT TGGCCAGGAT GGTCTTGATC TCTTAACCTC 120 GTGATCCGCC CACCTCAGCC TCCCAAAGTG CTTGGATTAC AGGCGTGAGC CACCACGCCA 180 GCCTGTGTCT TTCACACACA CACTTGCTTG TGCACCCACA AACACAGACT AGTTTGCCTG 240 GTACGTTGAC ACTTCCAACA TACACCTATT GGCAAAGGTT TACCCCGCTG GTTTCTGTGT 300 GGGTCCTAGA CGCTGGGAAA GGCACTGTGG CCCCAGGTGC TCCAGGGCCA GTGTGTTCTC 360 GGAGGGGCCA GGCATTTGGG ACACTTCATA ATCCTGGAAA GTTAGCGACC ACATCGTAGA 420 GTAGTTCGGG CAGGGCCTCC TCTGGTCACA GAGCCAGGAG GGGGCAGGAT CAGCACCCCC 480 ATCACCATTT CCATGTTTCC AGCACTCCAG TGAATAATCA AAGAAAGTTA AACAAACATG 540 CTTTAATTGC CTGTCGATGA CAGATGCCAA GGGAATGAAA ATCCCGTCCG GTTCTGGAGC 600 GCCTGCCCGG GGATGGGGGT GGTGTGGGGA GTCCGAGCTG GCTGGGCCTC TAGGGCCTCA 660 CCACAGCTGG GGAGCTGGAC CCACCCCACA ACCCCCATGT CCACCGTTGG CCAAGCTGCT 720 CCTCACCTGC CAAGCAGGGT GCCCAGTGCC AGAGCAAACT GGGCCCAGGC CCAGCATAAT 780 TTCCAGAAAT AGGTCTTTGA GAGAGCTGGG CCTCCCCCTC CATCCGCTGA ACTTCCACCA 840 TGCAGGGGAT CCTATTTGTT GCCTCAGGCC CTTGAAACAC TCTGCTCAAG GCCCCTAAAA 900 GCCTCCAGAT TGTGCAGTTT GCCCAGAGTT CCTGGACAGG CCAGGGCTGT CATTTGTAAC 960 TTCCCCATGT CCACCTCCTC CTCCTCTTCC CTCAGGCCCC AAGGGTGGGG TGGTGTCTTC 1020 CTGTGTGGCT CGAGCTGGAG AGTTGCTTTT CCCTTCCCTC CCCTTCCCTC TCCTCCCCTC 1080 CTCTCCCCTC CTGTCCTCTC CCTTCCCCTC CCCTCTCTGA CAGGGTCTGG CTCTGTTGCC 1140 CAAACTGTAG TGCAGTGGCG CCAACATGGC TCACTGCAGC CTCAACCTTC TGGACTCAGG 1200 TGATCCTCCT GCCTCAGCCT CCAAAGTAGC TGAGACTACT GGCACGCACC ACCATGCCTG 1260 GCTAACTTTT GTATCTTTTT GTACAGACAG GGTCTCACTG TGTTCACCAG GCTGATCTCA 1320 AACTCCCGGG CTCAAGCGAT CCACCCACCT CAACCTCCCA AAGTACAGGG ATTCCAGCCA 1380 TGAGCCACCA CACCCATCCT TCTTTTCTTT TTTAAATATG TTATTTTATT TTAAGGCTAG 1440 GTGCTGTGGC TCACGCCTGT CATCTCAGCT CTTTGGGAGG CCAAGCCGGG TGGATCACTT 1500 GAGGTCAGGA GTTCGAGACC AGCCTGGCCA ACACAGCGAA ACCCTATCTC TACTAAAAAT 1560 ACAAAAATTA GCCAGGCACG GTGGCACGTG ACTGTAGTCC CAGCTACTTG GGAGGCTGAG 1620 GCAGGAGAAT CACTTGAACC CCGGTGGCAA AGGTTACAGT GAGCCAAGAT TGTACCACTG 1680 CACTTCAGCC CAGGCAACAG AGCAAGATTC 1710
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