| Tag | Content |
|---|
EnhancerAtlas ID | HS184-02413 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr1:210464700-210467050 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Crx | MA0467.1 | chr1:210465540-210465551 | AAGGGGATTAG | + | 6.32 | | RREB1 | MA0073.1 | chr1:210465623-210465643 | CCCCCCACCACTCCCCGCCC | + | 6.25 | | ZNF263 | MA0528.1 | chr1:210465321-210465342 | GGGGGAGGATGGGAAAAAGGG | + | 6.97 | | ZNF263 | MA0528.1 | chr1:210465324-210465345 | GGAGGATGGGAAAAAGGGGGG | + | 7.27 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_30833 | chr1:210464132-210470056 | Fetal_Muscle |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I210290 | chr1 | 210464301 | 210469543 |
|
Enhancer Sequence | TAATAATCCC TCTCCTGAGA TCAATTACTA GGATTTATCT GGTTCCTCGA GCATAAAAGT 60
GTTTTATTGT TTTTACTTTT GCTCCAAGTG AAGTGTGAGT GGGTAGGCCA GGTTAAAATG 120
GACTGTCCCA GACAAGAATA TGAAGCTGGG ATCATTGGCC CTGCTTTTAC TGTCTACCAG 180
GTCCTCATGA CCAGGAAAGG GGGGAATATT TGGAAGCCAC TTCCCTGGGG AGGCACCAGG 240
TCCAGATGTC CTCATCTCTG GCTATTTGCA CGTATATAGA ACACAGGTCT GCAGGTGCCT 300
AGGAAGGTGG GTGCTGTTCC ACGGGAGAAG CTGGAAAGCA GAACCAAGTT ACCATCTCAG 360
ACCAAATCGT TTTTCCTCTA GAATTTCACT GTAATCCAAA CCAGTTGAAC ATTTGAGAAG 420
AACTGGGTAC CATGAAAAGG GGTAATGGAA TTAGCTTTCA TGTTTTTCCA GGACTCTAAA 480
CCATATTTCC TGTCACAACT GTACATTATT AATACAAGGC ATCTGTTAGC GCACAACTGC 540
CTGAAAATGT GCACCCAAAA ACCTTACATC TGGTTTCAAT AATTTATTTC TGACATTTGT 600
AGTTGGTGGT GGTGGGGAGT GGGGGGAGGA TGGGAAAAAG GGGGGAATTA AAGCAAGATG 660
TTGCCTTTAA CCCATCAGAA GCTCCTGTTG GAGCCGAAAG CTGGAGTTCT TAACGTGGTT 720
TCTGCATTAG GTAATATATT AATTTAGCAG CAAATAGCAA GACTCCGGGC CTGGTGGGTG 780
TGGGTGCCCG CTCGCTTTTA TCCTGCCTTC TCTGGCTGCA GCAATTAGCT TCCTCTTGCG 840
AAGGGGATTA GGAGGACCAC CCCCCAGCGG CGGGGGTTGG GGGGCTCTCG CAGAGCTGTC 900
AGGTGTCATT CGGCTTACCC AGCCCCCCCA CCACTCCCCG CCCCTGCAAT TAACTCCCTC 960
TCCCGCTTTG CCAGCCCCTC ACCCGCACAG AGACAAAGAG GCCTGTTCCC GAGGTGTCCG 1020
ACCTCCTGCC CCCTTGGCGG GCCCCGCCCG GGTTCCTCCA GCAGGAATCG CCCCAGGCGC 1080
TGGGAGCCAG AGCTGGCCGG GTCTGACACC CGCCCCAGAC TTTCCACGAT CAGGTTTCAG 1140
CTCGACTAAC GAGGGGGAAA GAAAGAACGC GCGACTTCCG CGGGCCGGAG CCGCGCGGGG 1200
GCCCGGGGGA AACGCCGGCC TGGTCTGGGT GGGAGGGGAC GCGAAGAGGC TCCGGGCTCG 1260
GCCAGTGTCT GCCCCGGGAC TGGGCCCTGG GACTAGGCGG GGCACAGGTG TCCCAGGAGG 1320
GGGCGCCCTG ACTTGACGCG AACGGGCCAC CTGTCCCTCC CACGCCTGCG CTGCCACCCG 1380
CCCTGCTCCG CCATCGCCTC CTCCAAAGCT CCCCGGATCC TCCGAGGCGT CGTCGTCCGA 1440
GTTGTTCTGC GGGAGGAACT TCTGCTAAAG CCGGTCCTCG AGTCCCCCCC GCCTCAGGAG 1500
GGGCAGCGCC CGGATTGTCT TAAGTACAAC ACTTGCCAAA AGGGGCTCTT TGGGATTTGG 1560
GACTTTTTTT CCTAAGCAAC AGACGTACCT TTCCAGACTC ACCAACTTAG AAGCACAGGT 1620
TTTCTGTTTG TTTCATTATT AGACTTTCAA AGATCATCAT GTCCCACAGC CTCCTCCTTT 1680
TCCAGATGAG GGGACTGAAA ATCAGAAACA TTTTGCCTTT TGCTCAAGGT CACACAGCTC 1740
AAGTTCACTG GGCGGCTGGG ACTAGAGGGT CCGAATATTC TGCAGCTATG ATATGAAAAA 1800
AATAAGTTTG GCTGGAGGGT GGAGGGCATC CAGGTCTGTC CTGGCCAGCC GGCGGGGAGG 1860
CTCAGCCCAG GGTTCAGATT TTCCTGGAGC CAGTCCACCA GCGGTCAGGC CACATGTGAG 1920
TAATGAAGAA TTGAGTGTTG TGTACTTTAG GCTGGTCTCC CTCTTCCTGG CCCCCTTCCC 1980
CGGCCTTAAC TTCCTTTTGG AGTCCCTACT GACTTCTGGG TGTCCACCAT GGGCCCTGTT 2040
GGAAAAATTT CAGCTCCATC CCAGAATAAA AGGAATGAAA ACCTGGGGAA AGGAGCCAAG 2100
AAGGAAAAGC CACAAATTCG CATCTGGCCG AGGCAGAGGG AGCAGCTCCA AGAGCCTGCA 2160
GAAATGCACT GTGACTGCTG TTTGCAGAGG TTCAGCTGCC AGAGGCTCGG ATGCCCTCCT 2220
GGGTCCTGCT CCTGAGAAAT CAGAGCAGGC AAGAGAGAAG ACACATGTTC CCCACCAAAT 2280
TTTTCCTGCC GCCAAGTCCT TCAGGTTTCT GCAGACCATG GGGAAGAACA AGAACTATGG 2340
AGTCAGGCAA 2350
|
