| Tag | Content |
|---|
EnhancerAtlas ID | HS059-18471 |
Organism | Homo sapiens |
Tissue/cell | GM12878 |
Coordinate | chr16:87957540-87959370 |
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 | TTTTGAAGTG GCTGCATGAA GAATTTTTAA ATAATATAAC CACATTAAAA CTGAAAAGCC 60
AATCTGAGTT GCTTCTTGGG CATTTGAACT TGGAACAGAC CAACAAGGGG AGAAAAACCA 120
TTGGCAACTG AATAAATGAA TGCAAAAATC CCTGCTCCCT GGTCCCCGAA GCTGGCCTGG 180
TTTGTGCCTC CCAAGATCTG GTTGTCCCAC TTTCCCTCTT CTTCTCCGAG CTGGTCTTGT 240
CCTTCCAAGA AGTTGCACTT TGCTTACGTT GGCTGGAGTT GGGGTTACTG CTGCTGGCAC 300
TCAGCAAGCC CCACACGGGA AGCATCCGCG GGGGTTGCAG TGGAGCCTGA TGAAGCAACC 360
GTGAATGGCA CTGAGCATAC AGGCAGCGTG GCTCCTTCTC ACCTTCGAAA GGAGAGAGAG 420
ACACTGGAAG GACCAAGCCG TGGTGTTTGC GATGCACTGT GTAGGGCCTG GCACAGAGAA 480
GAAGCTCTCA CGCCCTGCCC CCAACAGCAG GTGCATTAGA GGCAGGAGCA GGCTCAGGCT 540
GGGCCTCTAC TCTCCATGGG GTGCCTCTCC CCGGGCTCCA GGAAGGCCTG CACATACGGC 600
TCAGCGCACT CATCCGTGGG CACCGTGCCT GCTCACTGAG GTCCCCTGTG TTGAGAATTT 660
CTAGGCATAT GCAGATTTAA GTGGCTGAAA TGCAAGCACC ATGTCATGAC GAAGCTGGGA 720
CGCAGCTGGG CAGACCTCCC CGTGACAGCA GGAGCTGGGG AAGCCCCGGT GAGCATGTTT 780
AGTGTAAGGA AGGTGAATGC TGCCTCCGCA TGCACAGCGA GAGGGCATGA AGGTGAGCGT 840
GGGGGCAGCG TCCCGCTTGT TGGTCCCGCT TGGATAACGC AGAAGCGTGG AAGCAGGTCC 900
GGGCATGCTG GCAGCCATGT GGGAGTTTCT GGGCAGATGT GGTGCTGAGT GCCGGCCTGG 960
GGTGGCCTCG ATTCTCTCCC TGCAGCCTTT GCAGTGGCCA TCCCTTCTCT CCCCAATCAC 1020
AGAGGAAGAA AAGGAGGCTC ATTTATGCCT TCAACTCTGT TCATCCGTCA ATTTGCTGAG 1080
TGCCTAGGAG GCCTGGCGCA TAAAATATCA AATAAGACAA AGACCTGCCC CAGCGGAGTT 1140
ACATCCTCAT GGGAGCAACA GTGAGTGAGC AAGATCCCCA GGCACGTGGG ACGCACCCGG 1200
GAGGAGGCAG ATGGGATGCC TGCCGGAGAG GATGTGGAGC TGTGGCTGCG GCTGCTTTGG 1260
GGCCCCCAGG TTTGATGATT CCCCAGGAAG AGTCACTGGG TCCAGCACAG AGCCACCCTC 1320
AGAGCTAAGC TACATTCAGC AAAAGGACGC AGAGCGAGAT CAGCCACGCG AAGAGGTGTC 1380
TGGGCTGTCC GGAGGGCCCC AGGCAGGAGC TTCTGGAGTC CTCACCAGGG AAGACGGACA 1440
GGACGGACTT AATTCTCCCC TAAACCAGCC GCAACACTGA ACCAGTGTGA CGTGTTCTGT 1500
ACCAGAGGAG CTCACTAGCA ACTCAGTGCC CAAGGGTTTA TTGGGAGCTG TTCACATAGG 1560
CACCTGATAC CCAGCACGTG GCCCAATTCC AGACTCGCAG CAGGAGGGAG AGCAGGCGTT 1620
CCGCATGAAA GCAGCTTACA GTGACACCAG CTGGTGCTGG GAAAACACCA GGTAGGACCT 1680
GGCAGCCAGT CCTGATAAAA ATGCAAACAT AATAGGCATA GAGAGAACCT TCCCATACCT 1740
CAGAGCATCT GCCTGGAACT TCCGAGAATC ATGGTGAAGG TTTGAAGAGA TGATCCGCAG 1800
AAGCCCTTGG CCAAGCGCTG GAACCCAGTA 1830
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