| Tag | Content |
|---|
EnhancerAtlas ID | HS121-07552 |
Organism | Homo sapiens |
Tissue/cell | LNCaP |
Coordinate | chr11:86106460-86108660 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| SREBF2 | MA0596.1 | chr11:86108328-86108338 | ATCACCCCAT | - | 6.02 |
|
| | 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 |
| GH11I086394 | chr11 | 86105847 | 86107750 |
|
Enhancer Sequence | TGCTTTGCTT CACGGGTTCC TCTAGGCACT AGCACTCCTT GCTGATCTGC TGATCTCATT 60
GGGCAGTGTT TCTCAATGTT TTGTAGCTCA TGTTCCTTTT AATGTATTCT GTCTGTCTCT 120
CCCTCTCTAA ATCCACCAAC AAAGAAGAGT TTATTGCATA CACTTTCTGT AGTTAAGTTA 180
AATAACAATG GACATTTATT CTTTTTTATC CCCCCTCACC GCGACGGAGT CTTGCTCTGT 240
CACCCAGGCT GGAGTGCAGT GGCACGATCT CTGCTCACTG CAACCTCGGT CTCCTGGGTT 300
CAAGCAATTC TCTCCTGCCT CAGCCTTTGG AGTAGCTGAG ATTACAGGCG CACGCCACCA 360
TGCCTGGCTA ATTTTTGTAC TTTTAGTAGA GATGAGGTTT CACCATATAG GCCAGGCTGG 420
TCTCGAACTC CTGGTCTCAA GTGATCCATC CGCCTCGGCC TCCCAAAGTG CTGAAATTAC 480
AGGCGTGAGC CACCAGGCCT GGCCCATTTA CTCTTTTTTA AAACTACCCT TGGCTCCTGG 540
AAATTCTGAT ACTACCTTCC ATTAACCTTA GTCCCTGCAG TATTAGTAAA ACTCTTCTCA 600
CCTGCTGAAC TTTCCACTAC TTTGTACCAC TTCTTCTGCC CTAGCTGCTG CTTCTTCCTT 660
CAGTTCAGCC CATTTCCTGT CCTTGCTCGG ATTTTTACCA CTAAACGGGT TAAACAGATA 720
AGTTAGAATA AGGAAACAGC TTTACTCCAT GAGCACAGTG GTTGTTACTG GTGGTTGCAT 780
ATTACTGTAT TTAATCTTCA CGACAACCAT GTGACTTATG TATTATAATT CTCCATTTTA 840
TCATGATACA AAATTAATTT TAATTTTTTT CTTTTACATG AATGAAGCAA CATGGTGCAC 900
TATTGAGAAC ACTGGAGTAG GAGTCAGGAG ACTTTAGTTT TATTTCCAGT TTGGCCATCA 960
CTTATTCATT GTGTGCCCTT AATTATGTTA ATAATCTTAA TTGCTGTGCC ATTAACCACT 1020
GTGCATTTCA GGTGGAGGAA GTTTGGGGAA TAACAACTAG CTTCCTAAAG CATTATTACT 1080
TTAGGAAGTA TGAGTAAAGT ATAAAAGTAT GAGAATTTCT GAGATGTTTT GAGTGTGACA 1140
TTCTCTTGTT TGTTGCTTTG GAACAACCCC CTCCTGGAAG AGCTGTATGA CACATACCTC 1200
AGAAGATTCA GTGTGAAGTC CAGAGTAAGC CTTAGAGGTT GTTTTCCAAC CGCCTCATCT 1260
TGCACACGAA ATGGCCATGC AACTAATAAG CAGCCAAGCT TATAGAAATA AAACCATGGC 1320
TCCTGGTCCA GTGTTCTTTC CATTGCACCA TATTGCCTTA CTCACTAAAA ATAAATCAGT 1380
GGATTGAAAA GAATTTTATT TTGATGGTTT CGGAAGGCAA ACATGGCTGT TCCCTTTGAC 1440
ATATTTTGGC TTAGGCACTC CAGGAGGGAA ATAATTATAG TGGGTCAAAG AACAGAGATG 1500
GAGTCGCCAT CAAGTCAAGG GCCTAGAAAT GGACATGGGG ACTTAAATAC TCAAAACAAT 1560
TGTTGGTGTT TTATTTATGT GACATTTGGC CCCTGAATTG ACTGAAGGTA CCCCCACCCC 1620
CACTCCCTAC TCCAACCTAG TACTCCATAC CTGAGGCCAA AGAAATCCTA CAACTACACA 1680
CACCAACTGA ACATCCCCCT TCCTCCCTGC TGCAAATTGT AGCTTTGCAA GTCCTTCACT 1740
TTTGCCTGGG GAGAGAATGA TGAAGTGAAG TGGCAAAGGA GGGAGGAGAC AAATGGTTAT 1800
TTTGGGGCAT ACTCTACCAG GCTATGAATC TTTGCCTTCA AGCTATCCAA CAACCTTTTT 1860
TCCACTGTAT CACCCCATAG CATCTAGTTA AAGAAGTAGG ATATAAAAAT TCAAATTGAA 1920
ACAAAAACCA ATAACCTAAA TAAAGGACTT TAAGGCAATT TCTCTATATG CAAGCTGCTT 1980
TGAGACTATG GTATAGAGGG AAAGGCCTTG GTCAGCTTCC AGAAAGCCTT GGAGAAAATT 2040
AATCTATGAT ATGTACTTAG CACATCAGAG CACTCACCCC TTGAAGAAAG TGGGCTTATT 2100
TCAGAATCAG CCAGCTGGCT GGGTTGCTTC CAAAACTTGA GAGTTCACAC AGTTACCTGT 2160
TCAGGTTCAG TGCAGCAGAA AAACATATTG GCTCATTCCT 2200
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