Tag | Content |
---|
EnhancerAtlas ID | HS086-03298 |
Organism | Homo sapiens |
Tissue/cell | HEK293 |
Coordinate | chr13:99135790-99137560 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Stat4 | MA0518.1 | chr13:99136499-99136513 | CTTCCAGGAAAACA | + | 6.01 | Tcf12 | MA0521.1 | chr13:99136603-99136614 | AACAGCTGCTG | + | 6.32 |
|
| Number of super-enhancer constituents: 11 | ID | Coordinate | Tissue/cell |
SE_09852 | chr13:99135892-99138456 | CD14 | SE_27318 | chr13:99134618-99138372 | Esophagus | SE_32245 | chr13:99134667-99138347 | Gastric | SE_37511 | chr13:99132484-99138500 | HSMMtube | SE_38638 | chr13:99134504-99139239 | HUVEC | SE_42842 | chr13:99134593-99138841 | Lung | SE_44584 | chr13:99134588-99137561 | NHDF-Ad | SE_45616 | chr13:99132681-99141162 | Osteoblasts | SE_51002 | chr13:99134639-99139018 | Sigmoid_Colon | SE_53242 | chr13:99134682-99138361 | Small_Intestine | SE_65772 | chr13:99133027-99137514 | Pancreatic_islets |
|
| Number: 1 | ID | Chromosome | Start | End |
GH13I098482 | chr13 | 99134655 | 99140548 |
|
Enhancer Sequence | CCCTTTGAGA ACACGCCCCA ACTTCCCAGG CCTTTTTGCT TTTGGAGGTT CCGCAAGTCA 60 GGAAAATGCT TCACTTGTCT TCCCTCCCCA CGCCCTGGGC AAACTTTACT TTTATTATCT 120 ATTGCTCTGA TTTTCATTTC AGGTTTACTT CTCTGCATTT TCCACTTAAC AGCAAACTCA 180 AGTGCTCAGG GACAGCGCTG GTGTGCTCGA GCTCAGTAAA TGTTAACTGT GGACCCTGTG 240 ACCAAGGAAG AGTAACTCGT GTTGACTCTA GGGAGGCGCT AACGGTAAGA TGCACTGCAT 300 TTATAAAATA CATTCCTCTC ACAATTCAAA CTAAATCCTG CCATCTGGAG TTGATTCTAA 360 GACAGTCCAA ATAAACAGCC CAAGTTTTAA TGTATGTTGA ATGCTTTTCA AGCGTTTAAA 420 TGCCCTTGAC TGCTAAGATA ATAAAGACAA CTTCAGTCTT GACCGGACAA GTGCGGAAAC 480 CTCGAATGAT GTGTCTGACA CCCAACTCAG AGGGACAGGC ATGTCGCTCA TTCAATAACC 540 ATCCAGTCAC GGGCACCTGC CTTGAGGAGG CTTGGTGATC CCAGGTTCTG ATTTCAGGGA 600 AGCTTCCATC ATCAAGAGTG TCCTTCAGCA CACCTTCATC TCACACACAC GCTCGCCTGC 660 AGGCTTCCAC AATGCTTGCT CCTGGGGAAT GGGTATGCCA CAGTAAGCTC TTCCAGGAAA 720 ACACCAGTAT CTTTCTAGAT GGCAAAGGAA ATCTAAATCG CTTTTCCCTA AGAGAGCTGG 780 GAACTCTGAC GTTTCTACTC CCACTCCCTT TTTAACAGCT GCTGTTTAAC TGGTTTCACT 840 GGCTCCCATC CCTTCTATTT TCTGGGCATT AAGTCTGCTC ACAGCAAGGG GAGCTCCCAG 900 CAGGGAGGTA ATCTCCCCGC CTCTTCTCCC ACTGTAGCCA GCTGTGCAAT ATGACACCCT 960 GGGAAACAAT CTTTTGCTGA CTTAGGGGAC TGAGGGTCAC CAGGCAGCTT CCTGGAGCAG 1020 CAAGGCACAA GTGACCACCC CCTCGTCCTT CTGCACTTCC AAAGCTCCGC CCTCCTCAGT 1080 TCGCTGCTCT CTCAATCTGA CCACGAAGGT ACGTCACCAC TTGCCAAGCA AACAAGATAA 1140 GTTTCACCTG GCTACCTTCT CCTTTTAAGG AGCCCTAGCA AGACACCTCA ACCAAGTTTT 1200 CTGTGTCGCC CTGATCCTTC TGGGGACGTG CAAGCAACAA CAGAACATCC AGAGCTCTCT 1260 ACCCAGAGCA AACCCCGCCT CAGGACCAAG GCCGCCTCCT TCCTGGAGAG GAAGATGGAG 1320 AAATAACACA GCCTTCCCGC TTCCCTCCAA CTCATTCCTG GTAGCAGACG CGCTGGGTGG 1380 CAAGGCTACC CAGACACAAG GCTCACCAGA GGGCACTCAG GAAACCAGCT CAAGTCCTTA 1440 TTGAGGTCAC TGCGTCTCAA ATACCCGGGC TGGGCCTGTG ACTCACACAC CAGCACCAAC 1500 AACCAGGGGG TGGGATATTG CATCAGGAAA AGCTCCACTC TGGGTGGAAC CTGCTTTTCA 1560 ACCTCATTGG GTGTGTCACC GCCCAGTGGG TTCACCTTGC CCGCTGCCTA GACAGAGCCG 1620 ACTCATCAAG ACAGGGGAAC TGCAGTTGAG AAAGAGTAAT TCACGCAGAG CCAGCTGTGC 1680 AGGAGACCAG AGTTTTATTA TTACTGAAAT CAGTCTCTCC GAGCATTCGG GGAGAATTTT 1740 TAAGGATAAG CTGGTGGGGT AGGGGAAGCC 1770
|