| Tag | Content |
|---|
EnhancerAtlas ID | HS182-19437 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr6:168134280-168136350 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| TEAD1 | MA0090.2 | chr6:168135072-168135082 | ATGGAATGTG | - | 6.02 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr6 | 168134351 | 168135412 | | chr6 | 168135695 | 168135858 | | chr6 | 168135864 | 168136350 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH06I167733 | chr6 | 168134254 | 168135592 |
|
Enhancer Sequence | CAACTCTCAC CTGAGTTCCT GTCTCTCCAA CTCTCACCTG AATTCCTGTC TCTCCATCAT 60
CTCTCACCTG AGTTCCTGTC TCTCCACCTC TCACCTGAGT TCCTGTCTCT CCACACCCTC 120
ACCTGAGTTT CCTGTGTCAC CTGTTGTAAC AGCCCTCTCT TAAGAGGTCA GCTGGTTAGG 180
AAGCTCCAGT GTGAAAACCG TCCATAGGCA TTGGTGGTTC ACGGGACATT TTCCTTGGCA 240
GAAACTTCAG TTTTACTGAG AACTGAGCTG GAAATGTACG TGTAAGCACA AGAGGCCTCC 300
CAGAGCATTT GACCCAAATC CAGCACCAGT GTTGCATCCT CTTGCTGTAA AATAGGACAT 360
TTTTTCAAAA GGAGTGTGAA GTAAGTATTG ATTCACAAAG TGCCCTGAAG TCCTTGGATA 420
CTCCTGTCCC TGAATTCCCT CCGTGGATTC CCCACCCCGT CTCTCAGTGT TTGGACAAGC 480
GTGGGTTTTC TGACCAAACA TTCTAAACAA TGGCCTAAAT TCATCCCTGA GAGGCTGGCA 540
TTCAGCCTTC TGTTTTCAAT CTTTTTGAAC TCAACTGTGT ACTTGGACTG AGATTTTACA 600
TTGTGCAACT TCCTGACAGT AACGTGCCAT TACCCTGGGG GGTAAAGGGC TATTTAAGTC 660
CAGACTCAGC CATTCCCACC AGCCACAACA GAGCCAGACC TCTCCGTGCC CCGGGAGGGT 720
GCCCTGAACT CAAAATGTCC CTTGGCGATT GGGTTTAATA ACAGCATTTT CAAAGGCACT 780
CCCCAGTCCA CCATGGAATG TGGAGGCTGC CTCCTCTCCT GCCTCCGCTT TGCGGCACAG 840
CTGTGGCTCT GGGTCCCACA TGACTGCACA AAGTCAATGC CAAGGGCGTG ACCAGGGTGC 900
CCGAGACCTC ACTGTGGTCT GGGTGGAGCC CCAGCACTCA GGGTGCAGCT GCGCAAAGAT 960
TGCAGGCGCC TCTCCTGGGG CCTGAGCTTG TAAGTGTCCT TTGGATGTTG GGATGGGACA 1020
CCTGACTCCT CAGTAGGGCA CAAGGGGCCA CTGTAGGAAT AAAACTCAGA AAATCCCCCT 1080
GTTCACACTC AGCAACAGCC AAGCCCCCTT CAGTGTGATG CTGTGGGTGC TGACCTACAA 1140
ATCCTCACCC AGACACCTGC CACCCCGGAC CCCACAGAAT GGGCAGGACG AAGATCCTCC 1200
TGGTTTGGGG CGAGGAAGTG ACACCCTGGT CCCAGGACAT CTCCAGGGTC CTCTGTCAGA 1260
TACACACCCT CACCAAGCTG GCAAATAGGA TGTGTCCCCA TTTCACAGAT GAGGAAAGTG 1320
GAGCCCAGAG AGCTTCCACG ACTTTCCCAG GGTTGCAACA GAGCGAGGAG GGTCAAAAGG 1380
AGGATGGAAT GGGCATGGCC CCCAGCCCGT CCTTGACCAC CAGTTCCTTC CTCTGTCTCC 1440
AGTTCCAAAG GGGTCATCAC AGAGCACTTT GAAACCCCAG GGCTTCCCCC ACCGACCTCC 1500
CCCACTGACC TCCGCCGCTG ACTTCCCCTG CTGACCTCTG CCACTGACCT CCCCCTCTGA 1560
CCTCTGCCGC TGACCTCCAC CGCTGACCTC CCCCGCTGAC CTTCCGCCGA CCTCTGCCGC 1620
TGACCTCCCC CTCTGACCTC CGCCATTGAC CTTCCCTGCT GACCTCCACC GCAGACCTCC 1680
CCCGCTGACC TCTGCCGCTG ACGTCCCCCA CTGACCTCCC CCTCTGACCT CCGCCACTGA 1740
CCTCCGCAGC TGACATCCCC CGCTGACCTC CCCCGCTGAC CTCCGCCACT GACCTCTGCC 1800
ACTGAACTCC ACTGCTGACC TCCCCCACTG GCCTCTGCCG CTGACCTCTG CCGCTGCCCT 1860
CCCCCGCTGA CCTCCCCCGC TGACCTCCCC CACTGACCTC TGCTGCTGAC CTCTGCTGCT 1920
GCCCTCCCCC GCTGACCTTC CCCACTGACC TCCCCCACTG ACCTCTGCCA CTGACCTCTG 1980
CTGCTGACCT CCCCTGCTGA CCTCTGCTGC TGACTTCTGC CACTGACCTC TGCCGCTGAC 2040
CTCTGCTGCT GACCTCCCCC GCTGACCTCC 2070
|
