| Tag | Content |
|---|
EnhancerAtlas ID | HS184-26398 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr6:50809410-50810800 |
Target genes | |
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 | chr6:50810199-50810217 | GAAAGAAAGGAGGGAAAG | + | 6.33 | | EWSR1-FLI1 | MA0149.1 | chr6:50810195-50810213 | GGAAGAAAGAAAGGAGGG | + | 7.04 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH06I050841 | chr6 | 50809703 | 50811089 |
|
Enhancer Sequence | GGTGGGGGCC TGGGAGTGTG TGTTTGAACC CCACAGGTGT TTCTAAGGTG TACCTCTTAA 60
GAGCTTAAAA ACTGCCCCAC TTTGGTCAGA ACCCTTATCT ATTTCTTCCT GGTTGTGAGG 120
ATGTATGTGT GTACTTCAAA GGGAGAATCG AGGGTGCCTG TTAGTGTTCT CTATCCACCC 180
ATCTTAAAAC CAGCAACAGT TTAGCTTCTG TGACTGGGTG GTATTCCTCA TCAGATTTAG 240
CCACTATCCC AAAGTGGCAG CACCCTAGGA AAGGATGCCC CAGGATTCTT TGAGTCCAAT 300
CACCTGCCCT GTTTACCTGT TGGCTAGGCC AGGTGTGGCC AGGTATCTGT GAGTCGGGCC 360
AACCCATTGT GGGTCTAGGA CTGGAGTGCT GTAGGTTTAT TTTTTTCCTA AACCCCACAG 420
ACCCATAGGC TGGGTACAGG CAGGTGGACA TGAGAAATCT GCCCATCTGT GAAAAGCTGT 480
GGCCTTTGGG ATGCTGTGTG TCTGCCTGCC AGCCATTTGA CCTTCAGGGC TAGAACCATC 540
CCATCCAGCT CCTATATTAA AATTTCTCAA ATAAGCTCAA TCCATAGGTA GGCACGCAGG 600
ATTTCTAAGG CTGGGAGATT CCTCTAAATT GTAGGTGGCT TGAGGAAATA AAAACCTTCA 660
ACAAATAAAA ATCTATCCTC CCTAGTGTCT TAACAGCCTA CCTTTAGGTT TTATTTAAAC 720
TATATGGGAA TCCTTTTATA TTGACAACAG TCTGGTTATA CAAAGATTTT CAGTGCCCTA 780
CACTTGGAAG AAAGAAAGGA GGGAAAGGCA GAAACTAGCT CCCTCCCCCA ATACTGCAGG 840
TAAACAGGTT TTTGCTTTGA ATGGAATCAG CATTCTCTAG AATAAACAGT TTCTTGCCCT 900
GGGCCATGGA AGGCTCCAGC AATCTGCTTC AGTGCCAGGG ACAGGCTTGT GGCCGAGGGG 960
CCTAAATCTT TCAGGGCTTT TTGCGCCTGA TCACCAAGAG GTTGGAGAGG TGGGAGGGGC 1020
GCGGGGGAAA CAGCTCAAAA GAAATGCCAG GTAAGAGCTC AATATTATGA AGTATTAAAA 1080
ATCAACTGCT AAAGCCTAGC GAATGTCCCA AAGCGAGTCC AGGCGGTCCT GGAATGGAGG 1140
GGAGAAAGGC TGAAGTCGGG GGAAGGCAAG GCTTTGGGGT GGAAGGGGTG CATTACCTCC 1200
CCACCCCCGC TTTCCTTTCA GTCCCAGCTG CTCGAGAAGG GAGGGCGCTG GGAAAGGAAA 1260
CAGAGCGGAA TCGCCCACAT TAGCCTCGCT CTTCGGTGAC CCGGCGCCTC TGGGCTTGTG 1320
TGAGCGTCTC CTTTCTAATG CCAATGACAA CGACACTGAG GGTGATTTTC TGTGCCTCGC 1380
CCACCCCTTT 1390
|
