| Tag | Content |
|---|
EnhancerAtlas ID | HS121-18888 |
Organism | Homo sapiens |
Tissue/cell | LNCaP |
Coordinate | chr19:4364220-4365470 |
Target genes | | Number: 12 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| SOX10 | MA0442.2 | chr19:4365116-4365127 | AAAACAAAGGA | + | 6.32 | | SP1 | MA0079.4 | chr19:4365446-4365461 | GGTGGGCGTGGCTTC | - | 7.51 | | SP3 | MA0746.2 | chr19:4365446-4365459 | GGTGGGCGTGGCT | - | 6.78 | | SP4 | MA0685.1 | chr19:4365444-4365461 | ACGGTGGGCGTGGCTTC | - | 6.69 | | SP8 | MA0747.1 | chr19:4365446-4365458 | GGTGGGCGTGGC | - | 6.62 | | Sox3 | MA0514.1 | chr19:4364285-4364295 | CCTTTGTTTT | + | 6.02 | | Sox3 | MA0514.1 | chr19:4365116-4365126 | AAAACAAAGG | - | 6.02 | | Zfx | MA0146.2 | chr19:4364669-4364683 | CCCGCCTCGGCCTC | + | 6.01 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_26598 | chr19:4364974-4366059 | Esophagus |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH19I004364 | chr19 | 4364975 | 4366059 |
|
Enhancer Sequence | GTGGAGAAGT GGTGGGGGAA GCCATCATAC CGGGCCTGGG ACCACTAGAC TGAGACACTC 60
CTCAGCCTTT GTTTTTGAAA TAGCGTTTCA CAGGCTGGAA CGCAGTGGCG CTGTACCAGC 120
TCACTGCAGG CCTCAAACTG GGCTCAAGCC ATGCTGGCAC CTCAGCCTCC CAAGTAGCCG 180
GGACCACAGG CGTTCACCCC CACACCTGGA TCCTTTCCAA CTTCTTTGAG ATGAAGTCTC 240
GCTGTTGCCC AGGCTGCAGT GCAGTGGCAT GATCTCAGCT CACTGCAACC TCTGCCTCCC 300
AGGTTCAAGC AATTCTCCTG TCTCAGCCTC CTGAGTAAGG GGGATTACAG GGGCCTGCCA 360
CCACATCCAG CTAATTTTTG TATTTTTAAT AGAGACGGGG TTTCACCATA TAGACCACAC 420
CGGTCTCGAA CTCCTGACCT TGTGATCCGC CCGCCTCGGC CTCCCAAAGT GTTGGGATTA 480
CAGGCGTGAG CCACCGCACC CGGTTTTTGT TTTGTTTTGT TTTGTTTTGT TTTTTCATAG 540
TCTCGGCTCA CTGCAACCTC CACCTCCTGG GTTCAAGTGA TTCTCCTGCC TCAGCCTCCC 600
GAGTAGCTGG GGTTACAGGC ATGCACTACC ACACCCGGCT AATTGTGTGT GTGTGTGTGT 660
GTGTGTGTGT GTGTGTATAT ATATATATAT ATATTTTTTT TTTTTTAGTA GAAGCGGGGT 720
GGGGTTTCTC CATATTGGTC TTGCTGGTCT CGAATTCCCG ATCTCAGGTG ATCCACCTGC 780
CTTGGCCTCC CAAAGTGTTG GGATTACAGG CATGAGCCAC CACACTTGGC CCCATCCCAA 840
CTTCTAACAG CCCCCCAACA CTCTAAGCCC AGGGCCCGGA AATTGGAACT CAGGGCAAAA 900
CAAAGGATCC TAAAATCCGA ATCGATGCTG GACGTTAAAC CAGACCCTCC AATGCTCCTA 960
AAAGGGCCTA GGTTTGCCCT TAACAGGTGG AAGGACAGAT GCTGGGGGGT CCAGGCCCTG 1020
GGGAAGCAGC TGGCTTGAGT TGGGGAAGGT CTGGAGCTAC AGGAAGGGGC CCTATCAGCT 1080
GCTGGCCAGT GCTGGATGGG TTGGTCTGTG CAGTCTCCTG CACCTCTGCA GCTGGAAAGC 1140
TGTGGGGGCC ACTGTACGTC CCCGGCACTC AGCACATGCA GGGCCTGGAC CTGCCCTGCC 1200
TGTGTTGAGG TGTGGCCTCC AGGGACGGTG GGCGTGGCTT CCAGAGAGCA 1250
|
