| Tag | Content |
|---|
EnhancerAtlas ID | HS195-03031 |
Organism | Homo sapiens |
Tissue/cell | VCaP |
Coordinate | chr17:79693980-79695180 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| BHLHE40 | MA0464.2 | chr17:79694216-79694226 | GTCACGTGAT | - | 6.02 | | FOSL1 | MA0477.1 | chr17:79695136-79695147 | CATGAGTCACC | - | 6.62 | | Foxd3 | MA0041.1 | chr17:79695167-79695179 | GTTTGTTTGTTT | + | 6.32 | | JUND | MA0491.1 | chr17:79695136-79695147 | CATGAGTCACC | - | 6.02 | | Nr2f6(var.2) | MA0728.1 | chr17:79695075-79695090 | TGAACTCTTAACCTC | - | 6.53 | | TFEB | MA0692.1 | chr17:79694216-79694226 | GTCACGTGAT | - | 6.02 | | YY1 | MA0095.2 | chr17:79694583-79694595 | GCAGCCATCTTG | - | 6.74 |
|
| | Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
| SE_24622 | chr17:79694215-79694862 | Colon_Crypt_2 | | SE_24986 | chr17:79694274-79694842 | Colon_Crypt_3 | | SE_27510 | chr17:79694061-79695025 | Esophagus | | SE_41699 | chr17:79694211-79694856 | LNCaP |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH17I081727 | chr17 | 79694338 | 79695210 |
|
Enhancer Sequence | CAAGACCAGC CTGGCCAACA TGGTGAAACC CCGTTTCTAC TAAAAATCAA AAATTAGCTG 60
GGCATGGTGG CGCGCACCTG TAGTCCCAGC TACTCGGGAG GCTGAGACAG GAGAATCACT 120
TGAACCCAGG AGGCAGAGAT TGCAGTGAGC CAAGATTGCA CCACTGCACT CCAGCCTGGG 180
CTACAGAGCT AAACTGTCTC AAAAATAAAT AAAGTAATAA AATAATAAAA TAAATAGTCA 240
CGTGATGCTT CAGGTCATCT GACATCCTGC CCCCCACCCC TTAGTAAAAT GCCTGCTGTT 300
TTATTCAAGC AGCTACCACC CCACCCCAGT CCTTGGGCCT CAAGGGCACC AGGGCCTGAC 360
CCCAGCTCCC AGCATGAATA GGGTTGGTTT AAACCAGTCG GCATGGCCCA CAGTGACTGG 420
TTTAGGCATG GGCCTGTCAC CCACACTGGG CCAATGATAT GTAAGATGTT TATTGTAGCT 480
TCCGGGATGG AAACTTCTCT GCCAGCTTGT GGGTTGGGCA AGGACGACAC TCCGGGCCCT 540
ACCGGCGGAA GCTCTGCTCC TGTCGTGCGT GGACCACGCA GCAAATGGCC TTGGAGGCTG 600
CTGGCAGCCA TCTTGTGACC ATGAGGCAAG TCAGCGCAGG CCGAAGCTGA CGACGCGAAG 660
ACAATGAGGA GAGGGAGAAA GAGCCGATCT TTGGTGTGTA TTGGCTGTGA CGTGCTGCCG 720
CCTCTCTGGA GACCGGGTTC ATTATACTTT TCCTGGTATC TTCTCATGTT TGCTCTGCTG 780
GCTTTGGGCC CGAGTTTTAC CTCCTGGGTG TATTGTGTGT GCCTGTTTTG TGGTGTTGGT 840
TTTGCTCCTG GGTTTGTTGA CCCTTGGGTG TCTGCTCTTT TTTTTTTTTT TTTTTTTTTT 900
TGGGACAGAG TCTCACGCTG TCACCCAGGC TGGAGTGCAG TGACCTGATC TTGGCTCACT 960
GCAGCCTCTA CCTCCTGGGT ACAAGCGATT CTTCTGCCTC GGCCTCCTGA ATAGCTGGGA 1020
TTACAGGTGC CTGCCACGGC TAATTTTTTT ACTTTTAGTA GAGATGGGGT TTTGCCATGT 1080
TGGCTAGGCT GGTCTTGAAC TCTTAACCTC AGGTGATCTG CCCACCTCCG CCTCCCAAAG 1140
TGCTAGGATT TATAGGCATG AGTCACCGTA TCCAGCATTT TTTGCTTGTT TGTTTGTTTT 1200
|
