| Tag | Content |
|---|
EnhancerAtlas ID | HS184-12864 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr16:86003680-86004840 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr16:86003737-86003755 | CTTTGCCTCCTCCCTTCC | - | 6.33 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_61060 | chr16:85922118-86004487 | HBL1 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH16I085970 | chr16 | 86003724 | 86006248 |
|
Enhancer Sequence | TGTTTCAAAA ATATTTCGAA TGGAAAAAGT TTTCTTCTCT GGGGCAGTGG AAAGGGGCTT 60
TGCCTCCTCC CTTCCCATGC ACCACCCCCC ACGTCTGCTC CCGAAGCGCC TGATTCGTGC 120
TGTGCAGGGT TTGCATGTGC TGCTTCCCTT GGCTGGGGAT GCTCTCTCCC CAGCACCTTT 180
TGTGGCTATA CCTTTGTGTA AGTCAGATCT CTCTGCTCAA ATGTTGCCTC TGGTGGGGCA 240
TGGGTGTGGG TGGGGAGCTC ACCCATCCAA AATAGACAAC CCCCGTCCCC TTCCACACCC 300
CTCACCCATT TCTCTTCTTC CCAGCACCCA GCACTCTCTG GAGGGATTCT TTGCTGCCGT 360
GGAACCTCCC TACCACCAGT CCTGAGCATC TAGAGCGCTG GGCTCTGCTT CTGTTCACTG 420
TGGCCTCCCT GGGCCTAGGA TGATGCATGA CAGGGGGAAG GTGGCCAGAT GGAGGCTGCA 480
GTGCCACACG CGCCTTTCAG CACTGCGATG CAGAGGTCTC TTGAGAAGCT CTGCTTCCTC 540
CAGTTGGGGT GGCTACCACG TTAAGACCAC GTTTCCTGGG TTCAAATCCT AGTTGGGGTT 600
GCTTTTTGGG GTTCCTTAAT ATGCCTGTGC CTCAATGTCT TTATCTGTAT AATGGGGACA 660
AGACCAGGAC CTATCACATG GTGTTATGAG GATTAAATGA ATTAGTATAC GTGTCAGAGG 720
CATTTGAACC AGAGCAACTG CATCTTGAAA GCAGGCTCTG TAAAATAAGG CTGAGACCTG 780
CTGGGCTACA TTCCCAGACA GTTAGACATT CTAAGTCACA GGATGAGATT GGAGGTCAGC 840
ACTAGCTACA GGTCATAAAG ACCTTGCTTA TAAAACAGCT TGCAGTAAAG AAGCGTCCAA 900
ATCCCACCAC AATCAAGATG GTGATGAGAG TGACCTCTGG CCGTCCTCAC TGCTACACTC 960
CCACCAGCTC TGTGACAGTT TACAGATGCC ATGGCAACAT CAGGAAGTTA TCCTATATGG 1020
TTTAAAAAGG GGAGGCATGA ATAATTCACC TCTTGTTTAG CATATCGTCA AGAATTAACC 1080
ATAAAAATGG ACAACCAGCA GCCCTCGGGG CTGCTCTGTC TATGGAGTAG CCATTTATTC 1140
CTTTACTTTC CTAATAAACT 1160
|
