| Tag | Content |
|---|
EnhancerAtlas ID | HS076-46661 |
Organism | Homo sapiens |
Tissue/cell | H1 |
Coordinate | chr5:167791700-167793220 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| E2F6 | MA0471.1 | chr5:167792226-167792237 | GGGCGGGAAGA | + | 6.14 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_41838 | chr5:167791041-167793812 | LNCaP |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH05I168363 | chr5 | 167790773 | 167793942 |
|
Enhancer Sequence | CAGAGAGTGT CTCTGGGTCA CCCTCCAGCT CAACACAAGG GCAGTGGTCA GAGGAATAAT 60
CCAAAGTGCA TACCCAGGCC CCAGAGCCGC CAAAGCTGAC CTCCGCCTCC ACTTCACCTG 120
AATAGCATGG ATCTCTCTGA AATGGCCCTC TTGATTTGCT TCTGGCTGGG GTGCATCTCG 180
CCCTCTAGAC TGTAAGGGCA GGGCCCTATC TGTCTCTTTC CTCTGTAGCT GGTGTTAACG 240
AAGGCTCTGC TGTGTGTCAT GTGCTCAGCT CTCCTAACAA ACTTGAGAGA TGGTTATTTT 300
TATCATGCCC AGATTTGTTA GACAATGAGT AAAAGAGTCT GAACCAAACT GAATTAAAGG 360
AAGAAGGACT TCAAACGTTG CCTTTCTTCC TGTTCATTCT GGCCTCCCCG GAGCTAAAGG 420
TGAAGGGACT GCTTAGAAAT GGTGTTCTGC AGCAGCCCCA GGTGAAGGAG CATTATCAGG 480
AATTGTGCAA CCTTAGCTAT GGGAACTATG CGTGTGAAAC AGCCCAGGGC GGGAAGAACC 540
AGCCTGGCCA TTGTGCCTGG GCTGGGGAGG AGAGGTTCGG CTGAAAGTTT GGACAGTTCT 600
TGGCTTGGAG TCTGGAGGGC CCTTTAGAAA GTGATCCCGC CCAGCCAGCC CTCAGAGAGA 660
GCAGGCCAGC ATCCTGCTGG ACGGTAATAA AGAGGTTACT GTGGGAAGCT GGGACTTGCT 720
TGGGAAACAC TAGGAACATG AAAGATAGGG TATGCATTCT TCAGTCCCGA GAGAATCACC 780
ACCCAGTATT AAACTTGGCA GAAGGCTTTC CTCTCCTCCT CTGAGCTGCC TCCTTAGAAA 840
AGGCACATTG TCAGAATGCC GAATGCCCAC CGTGGTCTCA TGTCCTCACA GCCCGTAGGA 900
AAGTAACTAC CAGTTACCCA CTGGTGGTTG CCCCTGAGAG GAGGGTAAGG GAGGCTTCCA 960
GCCCCCGGGG TGGCTCTCCC CGACAGGTGT GCCTGTGTGC TGTTTGTAGG GTGCTCCTGG 1020
CAGAACCTAC CTGTCTCCAC AGCGACACAT CTGGCCGTTT TTCCAGGAGG GCCTGTTGAG 1080
AAACATTCAG GAATGTTTGT GCTCCTTTAG AGATTTGTAA TTAAGAAGAG GCAGAACTCG 1140
TTCTTGTCTG GCACCCTCCC TTCTTGCCCC TCCAGCATCT GGGTCATTTG ATTTCACAAT 1200
TGGGGTTTTC GGCAGCCCGA GTTGTGGAGG CTGGAAGCAG GGACCGACTG AACCAGGCTG 1260
GATGGTGGTG AATTGCTTCA CCCGAGGGTG GGGGCTGGGA GTTCCAGGCA GGCCCCCAAG 1320
TCCTGGCCAC ATCTGAAAGT GGACATTTCT TCCCAGGTTG CATCCTTAGC ACTTGCCCAA 1380
GGTGAAACAT TTCAGGCCAG TGGAGCACCC ACAGTTCCTG GGGGACGGGG GGTGGCTGGT 1440
TTAAATGGAC AATTCCTCTC CTTAACTGCC AGGAAGAGTG AGTGTGTGCA TGTATGTATG 1500
TGTGAGTGTG TCTGTTTAAA 1520
|
