| Tag | Content |
|---|
EnhancerAtlas ID | HS121-27799 |
Organism | Homo sapiens |
Tissue/cell | LNCaP |
Coordinate | chr3:127817790-127819430 |
SNPs | | Number: 2 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RUNX1 | MA0002.2 | chr3:127818642-127818653 | AAACCACAGAA | - | 6.32 | | STAT1 | MA0137.3 | chr3:127818922-127818933 | TTTCCTAGAAA | - | 6.14 | | Stat4 | MA0518.1 | chr3:127818919-127818933 | CTATTTCCTAGAAA | - | 6.51 |
|
| | 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 |
| GH03I128098 | chr3 | 127817109 | 127817924 |
|
Enhancer Sequence | GCATAAGAGA AGACTTAGAG TCAGTGCTGC TTTCTAAGGT GACTACAGAA GCCTCATCCC 60
CCTGCATCCC ACTCATCAAC TCAACATGGG ATCCTGAGGT ATGGAGACCC CTCCTCAAAG 120
CCTGAGGAGC TTCTAAACAC AGAGGAATTT TTAGAGGTTC CCCTAACCTG TAAGAATCAA 180
ACAAAATCCT TTCATGGCAA GTATAAGCTC CGTGGGGCCT GCCCAGCCTC CTTTTCCAGC 240
CCTATCTTTT TCCAACCCCT TGTTCCTTGA TTAGCCACAC AAGACTACCA GCCCTGCCCT 300
GGACACCCCC AAGCTTTTTT ATGACTCAAT GCTTTTGAGT CTATTCCATC TGCCAGGAAT 360
GCCATTCTCC TTCCTAGAAG TTCCCAGTCA TTAAAGTTCA CGTCAAATGC CCTCTAGGGC 420
GCATCTGACC CTAACCGGAC TCAGGACTTC CTCCAAATGT TCCTGTGCCT TTGGGGACAC 480
ATGGACTATA AGAGTAAGTA TAAAGAGCAA GTATAAATAT ACCATGATTA TATTGCTGTG 540
CCTCCTCTCA CTAGATTTGA CCACAGGCTT GCATCAGCCT AGTCCTTACT TAACTTGGAG 600
CTGATCATGG CTGACTCCAT AACAGGTTCA CCACTCACCT GCATCCTCCT GCGGGCTCCT 660
AACAGTGCAG TCAGCAAGAG GAAGAGGCTG GTGTTTGGTC ATTTATTCAG CATTTAGTGA 720
TCACCTGTTG GTTACCAGGC CCTGAGACAC AGAAGGGCTC ACTAAATGCT GAATAGCTAA 780
AGGCAGCAAA TGTTTCCTGT CTGGTCCTCA AAACTGCCTT GCCAAGTAGG AGGGAACTCA 840
AAACCGAACC CCAAACCACA GAAAACCCAG AGACCCAAAG TGACAAATTA ACCAAGCTGG 900
TCAGTGATGG AGCAACACAG TTCCTGACTT CTGACTCCCA GCCCAGCACT CTTCTCAGGT 960
CAAGGGCTCC CAGGAGGTCA GTTTGGGGAT GGCCATTTCA CCAACCAAGG GGACCTGTTG 1020
GTCCAAGATG AGTCTTCAGT AATCTCTTGA CCAAAGCTCC AAGGAACAAA ACACCCACGG 1080
ATCAAATTTC AAGTCAGAAA ACAAACTATT CCCTAATAGT GACTATTCAC TATTTCCTAG 1140
AAATGTCATA TAGTGATAAC ATCCTTTCCT GCACTTTACT AGCCAAGGCA TAAGTATCCA 1200
TCTGTATGAG AAGCAGACAA CAGTACCAGC TCAAAGCTAA AACACTGTGG CTTTTGCTAA 1260
GCAGGGGGAA AGAAAGAGCT TTGTTAGGCT TTCTGAAATC CTGTAAAGGG CTCATAGAAC 1320
ACTCCTGCCC TCCTGCCATT AACACCCAGA AAATCCCAGG TGTGAGCCCA CTGCTGGAGT 1380
GAAGCCATGG AGGAAGCTGG CTAGCTCAGG GCCAGAGGCT TGGCTGGGAT AAGAAACAAT 1440
ACACATGAAA TCATCTGTGA CTAGAGCATT TGAATGGGAA CAAAGGAGTC CCTCGTAGCT 1500
CATGTCGATG TTAATTGCTG AACATTACAG ATAGAAAAGG ACCGTCTACC TCAAGAAAGG 1560
CAGCAAGACT CTGACAATTC ATTCCCAGAT CTCCACACAC ATACAAAAGG GCTAATGTGC 1620
CAGATCACCC AGGCATCGAG 1640
|
