| Tag | Content |
|---|
EnhancerAtlas ID | HS051-10963 |
Organism | Homo sapiens |
Tissue/cell | Fetal_thymus |
Coordinate | chr16:87957550-87959400 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MYC | MA0147.3 | chr16:87959111-87959123 | CAGCACGTGGCC | - | 6.37 | | TP53 | MA0106.3 | chr16:87958431-87958449 | AGCAGGTCCGGGCATGCT | - | 6.37 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_65846 | chr16:87955784-87961349 | Pancreatic_islets |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH16I087924 | chr16 | 87957754 | 87958713 | | GH16I087925 | chr16 | 87958916 | 87959287 |
|
Enhancer Sequence | GCTGCATGAA GAATTTTTAA ATAATATAAC CACATTAAAA CTGAAAAGCC AATCTGAGTT 60
GCTTCTTGGG CATTTGAACT TGGAACAGAC CAACAAGGGG AGAAAAACCA TTGGCAACTG 120
AATAAATGAA TGCAAAAATC CCTGCTCCCT GGTCCCCGAA GCTGGCCTGG TTTGTGCCTC 180
CCAAGATCTG GTTGTCCCAC TTTCCCTCTT CTTCTCCGAG CTGGTCTTGT CCTTCCAAGA 240
AGTTGCACTT TGCTTACGTT GGCTGGAGTT GGGGTTACTG CTGCTGGCAC TCAGCAAGCC 300
CCACACGGGA AGCATCCGCG GGGGTTGCAG TGGAGCCTGA TGAAGCAACC GTGAATGGCA 360
CTGAGCATAC AGGCAGCGTG GCTCCTTCTC ACCTTCGAAA GGAGAGAGAG ACACTGGAAG 420
GACCAAGCCG TGGTGTTTGC GATGCACTGT GTAGGGCCTG GCACAGAGAA GAAGCTCTCA 480
CGCCCTGCCC CCAACAGCAG GTGCATTAGA GGCAGGAGCA GGCTCAGGCT GGGCCTCTAC 540
TCTCCATGGG GTGCCTCTCC CCGGGCTCCA GGAAGGCCTG CACATACGGC TCAGCGCACT 600
CATCCGTGGG CACCGTGCCT GCTCACTGAG GTCCCCTGTG TTGAGAATTT CTAGGCATAT 660
GCAGATTTAA GTGGCTGAAA TGCAAGCACC ATGTCATGAC GAAGCTGGGA CGCAGCTGGG 720
CAGACCTCCC CGTGACAGCA GGAGCTGGGG AAGCCCCGGT GAGCATGTTT AGTGTAAGGA 780
AGGTGAATGC TGCCTCCGCA TGCACAGCGA GAGGGCATGA AGGTGAGCGT GGGGGCAGCG 840
TCCCGCTTGT TGGTCCCGCT TGGATAACGC AGAAGCGTGG AAGCAGGTCC GGGCATGCTG 900
GCAGCCATGT GGGAGTTTCT GGGCAGATGT GGTGCTGAGT GCCGGCCTGG GGTGGCCTCG 960
ATTCTCTCCC TGCAGCCTTT GCAGTGGCCA TCCCTTCTCT CCCCAATCAC AGAGGAAGAA 1020
AAGGAGGCTC ATTTATGCCT TCAACTCTGT TCATCCGTCA ATTTGCTGAG TGCCTAGGAG 1080
GCCTGGCGCA TAAAATATCA AATAAGACAA AGACCTGCCC CAGCGGAGTT ACATCCTCAT 1140
GGGAGCAACA GTGAGTGAGC AAGATCCCCA GGCACGTGGG ACGCACCCGG GAGGAGGCAG 1200
ATGGGATGCC TGCCGGAGAG GATGTGGAGC TGTGGCTGCG GCTGCTTTGG GGCCCCCAGG 1260
TTTGATGATT CCCCAGGAAG AGTCACTGGG TCCAGCACAG AGCCACCCTC AGAGCTAAGC 1320
TACATTCAGC AAAAGGACGC AGAGCGAGAT CAGCCACGCG AAGAGGTGTC TGGGCTGTCC 1380
GGAGGGCCCC AGGCAGGAGC TTCTGGAGTC CTCACCAGGG AAGACGGACA GGACGGACTT 1440
AATTCTCCCC TAAACCAGCC GCAACACTGA ACCAGTGTGA CGTGTTCTGT ACCAGAGGAG 1500
CTCACTAGCA ACTCAGTGCC CAAGGGTTTA TTGGGAGCTG TTCACATAGG CACCTGATAC 1560
CCAGCACGTG GCCCAATTCC AGACTCGCAG CAGGAGGGAG AGCAGGCGTT CCGCATGAAA 1620
GCAGCTTACA GTGACACCAG CTGGTGCTGG GAAAACACCA GGTAGGACCT GGCAGCCAGT 1680
CCTGATAAAA ATGCAAACAT AATAGGCATA GAGAGAACCT TCCCATACCT CAGAGCATCT 1740
GCCTGGAACT TCCGAGAATC ATGGTGAAGG TTTGAAGAGA TGATCCGCAG AAGCCCTTGG 1800
CCAAGCGCTG GAACCCAGTA AGGGCTTGGT GGCTTTCAGG ACCTCTCAAG 1850
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