Tag | Content |
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EnhancerAtlas ID | HS184-13642 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr17:43488480-43490230 |
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) |
NR3C1 | MA0113.3 | chr17:43489916-43489933 | GGGGACATGGTGTCCTT | + | 6.07 | NR3C1 | MA0113.3 | chr17:43489916-43489933 | GGGGACATGGTGTCCTT | - | 6.1 | NR3C2 | MA0727.1 | chr17:43489916-43489933 | GGGGACATGGTGTCCTT | + | 6.08 | NR3C2 | MA0727.1 | chr17:43489916-43489933 | GGGGACATGGTGTCCTT | - | 6 | ZNF263 | MA0528.1 | chr17:43489296-43489317 | GGAGGAGCTGGGTGGAGAGGG | + | 6.03 | ZNF263 | MA0528.1 | chr17:43488635-43488656 | CCATCTTGTCTTCCCTCCTCC | - | 6.14 | ZNF263 | MA0528.1 | chr17:43489306-43489327 | GGTGGAGAGGGGAGAGAAGAG | + | 6.19 |
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| Number of super-enhancer constituents: 5 | ID | Coordinate | Tissue/cell |
SE_23758 | chr17:43485536-43490348 | Colon_Crypt_2 | SE_27799 | chr17:43481721-43494066 | Fetal_Intestine | SE_28693 | chr17:43481449-43494249 | Fetal_Intestine_Large | SE_42602 | chr17:43485387-43490334 | Lung | SE_52651 | chr17:43485072-43491303 | Small_Intestine |
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Enhancer Sequence | GGGCCAGGCA CCAGCTTCTT CCAGGAGGAA GGTTAAATCT TCTTCCTGGC CTCTCTTCCC 60 TTCACCCCCT CGTGTGGGGA TGACAGACCC CAGCCACGCA CAGTGGACAC ATGCCCTGAG 120 TAAGAAGTTA CAGCCCCTCC TCTGAGCCCA TGGGTCCATC TTGTCTTCCC TCCTCCCTTA 180 GAAGTGCTTC CTCCCCAGGC TTAAGGGCCA GGCAGCACTA AGCCCACCAG CCCACCCCTG 240 CTGAAGTCCA CCTCCTTTCC TGGTCAGGCT CTGACCCCCA CCCTTCCACT CTAGGCCCAT 300 TCTTCCTCCT CTGGCCCCCA CCCTGGATCT CTTTTTCTCC CCTGCCATGT CTCTCAGCCC 360 CTCTTCTCCT GTACCCACTG TGGGCTGGGG ACAAGGACCC CAAGCAGAGC CAGGCACAGT 420 GTGAATGTGG GGCACGAGAC ACTTGTAGAG ATCACACTAG GAGCAAGACT GGGCCCCATG 480 CCCTGCTCTG CCCACAAAAG CTCTCATACC AGTGTCCCAT CCCCTGTACC CGACTCAGAA 540 GCCCAGACCC CAGGGGTAGA CTAATCCCCT CCTCGCTATC AGGGTGGAGG ACAGCAGGAA 600 TCACAGAAGG CTGGAGGCCT CATGCTTATC ACACACCTGA CCCATCTCTC TGTCCCCACC 660 CTGAGGCCAG GGATGAGGAC TCACACACAC ACACACACAC ACACACTACA CACGTGTGCG 720 TGCATATGAC AGGTCACCAA GGGTTATGCA ACCAGGCCTC AGAGACAGGA ATAGCCTCTG 780 TAAATTCCAG AGAGGCCAGA AACTCTGAGC CACCAGGGAG GAGCTGGGTG GAGAGGGGAG 840 AGAAGAGGAC AGGTGTGGAA CTCAGGCCCT CAGCATTGCC CTGCAGGTAG CATGGGGGGC 900 AGGGACTCCC TATGGCAGAG CCAGGAGTGT CAGTGTCAGG GCTGGGACTG CAGAATGGGC 960 AGCCAGCAAC TCACCTGGCA TCTCACCTGC TTCTCTTCCC CAGTAGGAAG CTGGGCCCCC 1020 ATGATGGGGG TCTCCCAGGG GGCTCCAGCC CCAAACTATA GGGAGTGAAC AAACTCACAC 1080 AGTTCCTGCC TGCTCTTGGC CACAGAAGTT GGCTCTCAGG CCCTGTCTCG GATTCCCTCC 1140 CCCCAGTGAG AGGAGGTGAT GACCACAGTG GCTCCCCAGA GGGGTCCACC TCCCTCCACC 1200 ACACCCTCAT GCCTCTGAGA GGCACAAGGG GGAGGGTCAG GAGAGGTTCT AGAACAAACC 1260 AGCTGCACAA CACCCCTCCT TTCCCCACTC TGACCTCACT CTTCCCTCCC AAACCCTCAT 1320 AGGAAGTGCT GGGGCAGGAG CAGGTGCACT AGGAAGACCC AGTCCTCTGG GGCTAGAGGC 1380 AAAATGAACG CCTCCAAACC AGGACTTGGC CCAGGAACTG GCTCAGGGGC TGGCGAGGGG 1440 ACATGGTGTC CTTTGTTGAC TCAGTGAGTC TGCTCTGTGC CACCCAAGCC AGGTGGAGGG 1500 AGAGCCAGAA GGAATGGTGA TCTTTGCCTC AAGGAGCTCA GTCATGTCCA CACGACAGGT 1560 CCCTCCCCCA AACACATGTT CTCCAGGACA GAAACTGGGT CTCCCTTTAA CCATCCCGGC 1620 CTGGCCCAGA GCTACATGTC CAGGGGCAGG ATCGGAGGAG CTGGGGGTGA CCCCACAGGA 1680 TCCTGGGCCT CAGGCCTCAG TAGGCTTTGG GGAACTGTGC CTAGCTCAGC CCTCTGAGAT 1740 TCTGATGGAA 1750
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