| Tag | Content |
|---|
EnhancerAtlas ID | HS184-11380 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr15:67316040-67317190 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| JUN(var.2) | MA0489.1 | chr15:67316883-67316897 | GAAAGATGACTCAT | + | 6.69 | | MEF2C | MA0497.1 | chr15:67317011-67317026 | CATCCAAAAATAGCA | + | 6.67 |
|
| | Number of super-enhancer constituents: 9 | ID | Coordinate | Tissue/cell |
| SE_26536 | chr15:67315776-67319262 | Esophagus | | SE_27694 | chr15:67316001-67318713 | Fetal_Intestine | | SE_28551 | chr15:67316023-67318845 | Fetal_Intestine_Large | | SE_34728 | chr15:67315459-67319545 | HeLa | | SE_36559 | chr15:67315940-67318864 | HMEC | | SE_36917 | chr15:67315359-67319678 | HSMMtube | | SE_45534 | chr15:67315606-67319645 | Osteoblasts | | SE_47100 | chr15:67313358-67320816 | Panc1 | | SE_52344 | chr15:67315957-67319365 | Small_Intestine |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH15I067023 | chr15 | 67315665 | 67319555 |
|
Enhancer Sequence | GCAATGGGTT GGCCATTGCT TGTAGCTGCT ATTCATCTAG GAAGGTCCCA GCACCGGCCC 60
CTGTTTCCAC CTCCCGCAGC CCTCACATGT GGATCCACTG GTTTCACCTA CAGCTCCAAC 120
CTTGGCCTGG TTCACTGATC GATCAGCCTG AGGCTAGAAG CACTTACACA GCTGGAGAGC 180
AAGTCACTCT TTCTACTGGC ACCCAGCACT ATGCCTGCAG CACACACGTT GTCACACACC 240
TGTCATCCCC TTGGGCACTG GGCCTTTCCC TCCTGTGTAG CCCTCAGCTG GGTCAGCCTG 300
GCTCCTCCTG TGGGGGCGGG GGGCTGGCCC CAGAGCTGCC CTGGCTAAGG CCACAGGGTC 360
ATACTGGAAG TGAAGAGACC AGCCTCAACA AATCCAGGAA ACAGACCCAG GTAGGAGTGT 420
GAAGGGCATG GCTGTAGTGT GGGGTGTGGA AGCCCAATTC TGGGCTTCCC AGAATTTCCC 480
AGCAGGCTTG GGGGAGGGGT GGTGGCAGCT GGCCCAGTGG AAGGGAACCT CCATCCACCC 540
TAGAAAGATT GTCCCACTTT CCTTATGGGT CAGCACCTCA CAATGTCATC ACCAGAAGGG 600
CTTTCTTCCC CACGTGGATT ACATAGCAGG TAGATGGATT TGTGCTTGCA GACACAGAGG 660
GGCCAGAGTT TTAAAGGCCG TCAGTACCCT ATGGCCCATC TCAAAGAAAA AGACAAGGAT 720
AAGCAAAATT AGAAGGAAAG AAAGAAAGAC TGTAAAAGTT AAACAAAACC ACCCACAAAT 780
AGCTTGAGGC AGAAAAAAGA TTGTACCATA TCATGGCAAT CGTGGACAGT TTGGCAGCTG 840
AGGGAAAGAT GACTCATTCC CAGGCTCCGC TTGCATAATC CTCCCCAGCC CAGGCAGGAG 900
AATGAAACTA GGAAAGTAAT GCAATGACAT TTAGTAGCAA AAAGGAAGCC CACACAACAT 960
TTGTGCAAGG CCATCCAAAA ATAGCAGGCT CCTCCATGCT TGGGTTTTGA AACTATGCAT 1020
TTTGCTTGAA ATGCCTGAGT CGTGGCACAT TTTTCTTGGG CCACCCACAC CCTAATTCAG 1080
TTCATTTCAA TTTAGCAGAC ATTTAATGCA GGCCTACTGT GCTCCAGGCT CTGTGCTAAG 1140
GATTTGGGAG 1150
|
