| Tag | Content |
|---|
EnhancerAtlas ID | HS195-01368 |
Organism | Homo sapiens |
Tissue/cell | VCaP |
Coordinate | chr11:129723160-129724500 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NFE2L1 | MA0089.2 | chr11:129724313-129724328 | AGGTGACTCAGCACA | + | 6.38 |
|
| | Number of super-enhancer constituents: 5 | ID | Coordinate | Tissue/cell |
| SE_27353 | chr11:129722906-129725277 | Esophagus | | SE_27846 | chr11:129723063-129724609 | Fetal_Intestine | | SE_35121 | chr11:129721033-129725996 | HeLa | | SE_36539 | chr11:129723345-129724382 | HMEC | | SE_64293 | chr11:129722901-129725891 | NHEK |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr11 | 129723853 | 129724184 | | chr11 | 129723312 | 129724437 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH11I129852 | chr11 | 129722635 | 129725772 |
|
Enhancer Sequence | CCTCCAGGAA CAAGCAGTGA TGACAGTAAC AAGTGTTCTT CCTCAGGACC AGCCCCACCT 60
GGGGGGAATG AGGGGTCTTA ATCTGCAACT GACAATTACC ACTTGTCATC AGTGGCCTAT 120
GGCTTCTTGG AGAGAGTGAA GCAACATCGC TTCTCTTGGA GGAAGCAAAG CTTCACAGGG 180
CTTTGTTGGT CTCATCCTGC TGAATGTCCC CACTCACCAT TCAGGCATCA GAGAGGCCTC 240
CCGTGAGAAG TGACAGGGAC CTGTGGCTTA AAGGATCAGG ACAGCATCAA CCTTGCCTAA 300
ATAAAGCTAG GACAATTACA ATATTTGGCC CCTTGACTGG GTGAAAATGG TACTCATTCA 360
ACAGCTCTCT GGCACTCCTA CCACAAGCCA GGAAGTCACT GTTCCAGGCA TAGGAGATAC 420
ACTGGGGAAC CACACAGCCG CTGCTGTCAC AGGGCTTCCA TTCTAGTGTC ACTGGGACTT 480
TTCCTGGGTC ATTTCCACAA CTTCCTGACT CTGTGTGTGG GAATTCAAAA AGGGTCTGGC 540
TTGAGAAACA AGTATCTGGG AAACGGAGTC CAAAATGTCA TCATGGAGGA TTTCTTCTAG 600
GCTTCCCCAA GAACACTTTG GGTACCAGGC ATAAAGACAA ATCTTTTGCC TTCCAAATTA 660
GCTGATAAAA GTAGAAGGGA TAAGAACTAA GAGCTATCCT GTGTCGCAGT TTCGTCATTT 720
TCTGGCCCAC ATCCTGGGGC CTCTGCCTTG TTTACCCGGT GTTTTAAAAC ACACAGCTGG 780
GAGGGGCGCA GGGCTTGCAG AGCTGGCTCT GTGCCCAGGA AGGACACGCA CTCAAAATCA 840
GCCCTGCAGA CACGCACCTG GGAGCCGCTT CCCTCCCTTG GCACGTACAG GTATCTTCAT 900
TACCAGTGTG TCTCTGCTCA GATTCTGCTT TCAGCCTAAT TGTTTCTGTC TGGGATTTCT 960
TTCACTGCTC ACTTGGCAGG GAAGCCCAGA GATTATTCTA TCAGCCACAC TCCGACTTAA 1020
GTGATGATGT CTTGCTCATC TCTGCTCCTG GACAAACCTC CTGGGGATCT ATGTGTGTGT 1080
GGTTGTGTTC ATTGATTCTT CTACCCTCAA CCCCAAACCC CTAAAAGGAA CAACAATGGC 1140
AAGATGTCTA CACAGGTGAC TCAGCACACA CCCTACTTTA TACTGAAGCA GCTGCACCTG 1200
AGGCAGCAAA GTAGCTCTGC TGACCCGCGG GCCACCCTCA CCTCACCCCA TCTCCGCTTC 1260
GCTCATGCCT TTGGGTTATT CCTTGCTCCT ATTTGTCTTA GAGCTACTCT TCCCTCTAAA 1320
ACATCCATCC TCATTTCCCT 1340
|
