| Tag | Content |
|---|
EnhancerAtlas ID | HS184-09356 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr13:99136370-99137530 |
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 | CCAGGTTCTG ATTTCAGGGA AGCTTCCATC ATCAAGAGTG TCCTTCAGCA CACCTTCATC 60
TCACACACAC GCTCGCCTGC AGGCTTCCAC AATGCTTGCT CCTGGGGAAT GGGTATGCCA 120
CAGTAAGCTC TTCCAGGAAA ACACCAGTAT CTTTCTAGAT GGCAAAGGAA ATCTAAATCG 180
CTTTTCCCTA AGAGAGCTGG GAACTCTGAC GTTTCTACTC CCACTCCCTT TTTAACAGCT 240
GCTGTTTAAC TGGTTTCACT GGCTCCCATC CCTTCTATTT TCTGGGCATT AAGTCTGCTC 300
ACAGCAAGGG GAGCTCCCAG CAGGGAGGTA ATCTCCCCGC CTCTTCTCCC ACTGTAGCCA 360
GCTGTGCAAT ATGACACCCT GGGAAACAAT CTTTTGCTGA CTTAGGGGAC TGAGGGTCAC 420
CAGGCAGCTT CCTGGAGCAG CAAGGCACAA GTGACCACCC CCTCGTCCTT CTGCACTTCC 480
AAAGCTCCGC CCTCCTCAGT TCGCTGCTCT CTCAATCTGA CCACGAAGGT ACGTCACCAC 540
TTGCCAAGCA AACAAGATAA GTTTCACCTG GCTACCTTCT CCTTTTAAGG AGCCCTAGCA 600
AGACACCTCA ACCAAGTTTT CTGTGTCGCC CTGATCCTTC TGGGGACGTG CAAGCAACAA 660
CAGAACATCC AGAGCTCTCT ACCCAGAGCA AACCCCGCCT CAGGACCAAG GCCGCCTCCT 720
TCCTGGAGAG GAAGATGGAG AAATAACACA GCCTTCCCGC TTCCCTCCAA CTCATTCCTG 780
GTAGCAGACG CGCTGGGTGG CAAGGCTACC CAGACACAAG GCTCACCAGA GGGCACTCAG 840
GAAACCAGCT CAAGTCCTTA TTGAGGTCAC TGCGTCTCAA ATACCCGGGC TGGGCCTGTG 900
ACTCACACAC CAGCACCAAC AACCAGGGGG TGGGATATTG CATCAGGAAA AGCTCCACTC 960
TGGGTGGAAC CTGCTTTTCA ACCTCATTGG GTGTGTCACC GCCCAGTGGG TTCACCTTGC 1020
CCGCTGCCTA GACAGAGCCG ACTCATCAAG ACAGGGGAAC TGCAGTTGAG AAAGAGTAAT 1080
TCACGCAGAG CCAGCTGTGC AGGAGACCAG AGTTTTATTA TTACTGAAAT CAGTCTCTCC 1140
GAGCATTCGG GGAGAATTTT 1160
|
