| Tag | Content |
|---|
EnhancerAtlas ID | HS161-13127 |
Organism | Homo sapiens |
Tissue/cell | PC3 |
Coordinate | chr6:31169040-31170140 |
Target genes | | Number: 12 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| GSC | MA0648.1 | chr6:31169259-31169269 | GGGGATTAGC | - | 6.02 | | HSF1 | MA0486.2 | chr6:31169845-31169858 | GAACCTTCCAGAA | - | 6.19 | | Nr2f6(var.2) | MA0728.1 | chr6:31169462-31169477 | GAGGTCAAGAGATCG | + | 6 | | ZNF263 | MA0528.1 | chr6:31170051-31170072 | GGAGGAAGACTAGGAGAGGAG | + | 6.03 | | ZNF263 | MA0528.1 | chr6:31169083-31169104 | TTCTCCTCCACCTGCTCCTCC | - | 7.86 |
|
| | Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
| SE_23693 | chr6:31168877-31169331 | Colon_Crypt_1 | | SE_23693 | chr6:31169592-31172239 | Colon_Crypt_1 | | SE_32160 | chr6:31169700-31172832 | Gastric | | SE_53048 | chr6:31169658-31173115 | Small_Intestine |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH06I031201 | chr6 | 31168878 | 31169331 |
|
Enhancer Sequence | GTTGGCTGGG AACTCACTGA GGCTGTGAAC CAGGTGACTT GGTTTCTCCT CCACCTGCTC 60
CTCCACGTGC CCTGGCTGCT TCTGGCTCTG CACCTGGGGT CCGGGTGTTT CAAGTGGCCA 120
AGTCAGAACC ACAAGGCATC TTATGCTGGA ACCTCAGAAG TCAGGCAGCA TCACGTTCCT 180
CATGTTCTAG TCACCAAAGC AAGTCCCAGA TCCAAAAAGG GGGATTAGCA TCAGCTCTTG 240
ATAGAGGATG GCAAGGTCAC ATTGCTAAAG AGCATGTGGG ATGGGAGATA TTGTTGAGGC 300
CATCTTTGGA AAAGGACTTT TATGTTTACA AAGTGATAGG TGATAAAAAG AAAAAATAGG 360
CCAGGTGCGG TGGCTCACGC CTGTAACCCC AGCACTTCGG GAGACCGAGA TGGGTGGATC 420
ACGAGGTCAA GAGATCGAGA CCATCCTGGC CAATATGGTG AAACTCTGTC TCTACTTAAA 480
AATACAAAAA TTAGCTGCAT GTGGTGGCGT GCACCTGTAG TCCCAGCTAC CCTGGAGGCT 540
GAGGCAGGAG AATCGCTTGA ACCCAGGAGG TGAAGGTTGC AGTGAGCCAA TATCGCACCA 600
CTGCCCTCCA GCCTGGTGAC AGAGCAAGAC TCCACCTCAA AAAAAAAGAA AAAAAGTAAA 660
AAAAAAAAAA TGCAAAGTTG ACAATCAATG CAAAGTAATA GAGGTGGCAT TTTAAGTAGG 720
GTGGTCAGGG TGGGCCTCAT GAAGGTGCCA TTTGAGCAGA CTTGAAGAGG AGAGAAACTG 780
AGACACGCAG GTATGTGCAA AGGAAGAACC TTCCAGAATC ACCCTCATGT ACACCTATGC 840
TCTGTACATA CCCAGGGCTC TGCACTGAGG CAGACCCTAA AGCTGCAGTG GGAATGGAGG 900
TGGACACACT TATGGAAAGA CTTCTTCAAA GAATGTTGGG GACCCAGGTC TACCCTTCCT 960
GCTGTGGCTC TTATACGACG TGGAGTTGGG GAGGGAAAGG CACTGGCATG TGGAGGAAGA 1020
CTAGGAGAGG AGGGGAGGCC AAAGCGTGTC CCACCCTCAC TCCACCTCTC TGCTCTCTGT 1080
CTCCTACATC GAGTGCCTCC 1100
|
