Tag | Content |
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EnhancerAtlas ID | HS099-09627 |
Organism | Homo sapiens |
Tissue/cell | HSMMtube |
Coordinate | chr17:43488900-43490180 |
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) |
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 | chr17:43489306-43489327 | 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 | GTGAATGTGG GGCACGAGAC ACTTGTAGAG ATCACACTAG GAGCAAGACT GGGCCCCATG 60 CCCTGCTCTG CCCACAAAAG CTCTCATACC AGTGTCCCAT CCCCTGTACC CGACTCAGAA 120 GCCCAGACCC CAGGGGTAGA CTAATCCCCT CCTCGCTATC AGGGTGGAGG ACAGCAGGAA 180 TCACAGAAGG CTGGAGGCCT CATGCTTATC ACACACCTGA CCCATCTCTC TGTCCCCACC 240 CTGAGGCCAG GGATGAGGAC TCACACACAC ACACACACAC ACACACTACA CACGTGTGCG 300 TGCATATGAC AGGTCACCAA GGGTTATGCA ACCAGGCCTC AGAGACAGGA ATAGCCTCTG 360 TAAATTCCAG AGAGGCCAGA AACTCTGAGC CACCAGGGAG GAGCTGGGTG GAGAGGGGAG 420 AGAAGAGGAC AGGTGTGGAA CTCAGGCCCT CAGCATTGCC CTGCAGGTAG CATGGGGGGC 480 AGGGACTCCC TATGGCAGAG CCAGGAGTGT CAGTGTCAGG GCTGGGACTG CAGAATGGGC 540 AGCCAGCAAC TCACCTGGCA TCTCACCTGC TTCTCTTCCC CAGTAGGAAG CTGGGCCCCC 600 ATGATGGGGG TCTCCCAGGG GGCTCCAGCC CCAAACTATA GGGAGTGAAC AAACTCACAC 660 AGTTCCTGCC TGCTCTTGGC CACAGAAGTT GGCTCTCAGG CCCTGTCTCG GATTCCCTCC 720 CCCCAGTGAG AGGAGGTGAT GACCACAGTG GCTCCCCAGA GGGGTCCACC TCCCTCCACC 780 ACACCCTCAT GCCTCTGAGA GGCACAAGGG GGAGGGTCAG GAGAGGTTCT AGAACAAACC 840 AGCTGCACAA CACCCCTCCT TTCCCCACTC TGACCTCACT CTTCCCTCCC AAACCCTCAT 900 AGGAAGTGCT GGGGCAGGAG CAGGTGCACT AGGAAGACCC AGTCCTCTGG GGCTAGAGGC 960 AAAATGAACG CCTCCAAACC AGGACTTGGC CCAGGAACTG GCTCAGGGGC TGGCGAGGGG 1020 ACATGGTGTC CTTTGTTGAC TCAGTGAGTC TGCTCTGTGC CACCCAAGCC AGGTGGAGGG 1080 AGAGCCAGAA GGAATGGTGA TCTTTGCCTC AAGGAGCTCA GTCATGTCCA CACGACAGGT 1140 CCCTCCCCCA AACACATGTT CTCCAGGACA GAAACTGGGT CTCCCTTTAA CCATCCCGGC 1200 CTGGCCCAGA GCTACATGTC CAGGGGCAGG ATCGGAGGAG CTGGGGGTGA CCCCACAGGA 1260 TCCTGGGCCT CAGGCCTCAG 1280
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