| Tag | Content |
|---|
EnhancerAtlas ID | HS024-06270 |
Organism | Homo sapiens |
Tissue/cell | Cerebellum |
Coordinate | chr16:87957570-87959800 |
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 | ATAATATAAC CACATTAAAA CTGAAAAGCC AATCTGAGTT GCTTCTTGGG CATTTGAACT 60
TGGAACAGAC CAACAAGGGG AGAAAAACCA TTGGCAACTG AATAAATGAA TGCAAAAATC 120
CCTGCTCCCT GGTCCCCGAA GCTGGCCTGG TTTGTGCCTC CCAAGATCTG GTTGTCCCAC 180
TTTCCCTCTT CTTCTCCGAG CTGGTCTTGT CCTTCCAAGA AGTTGCACTT TGCTTACGTT 240
GGCTGGAGTT GGGGTTACTG CTGCTGGCAC TCAGCAAGCC CCACACGGGA AGCATCCGCG 300
GGGGTTGCAG TGGAGCCTGA TGAAGCAACC GTGAATGGCA CTGAGCATAC AGGCAGCGTG 360
GCTCCTTCTC ACCTTCGAAA GGAGAGAGAG ACACTGGAAG GACCAAGCCG TGGTGTTTGC 420
GATGCACTGT GTAGGGCCTG GCACAGAGAA GAAGCTCTCA CGCCCTGCCC CCAACAGCAG 480
GTGCATTAGA GGCAGGAGCA GGCTCAGGCT GGGCCTCTAC TCTCCATGGG GTGCCTCTCC 540
CCGGGCTCCA GGAAGGCCTG CACATACGGC TCAGCGCACT CATCCGTGGG CACCGTGCCT 600
GCTCACTGAG GTCCCCTGTG TTGAGAATTT CTAGGCATAT GCAGATTTAA GTGGCTGAAA 660
TGCAAGCACC ATGTCATGAC GAAGCTGGGA CGCAGCTGGG CAGACCTCCC CGTGACAGCA 720
GGAGCTGGGG AAGCCCCGGT GAGCATGTTT AGTGTAAGGA AGGTGAATGC TGCCTCCGCA 780
TGCACAGCGA GAGGGCATGA AGGTGAGCGT GGGGGCAGCG TCCCGCTTGT TGGTCCCGCT 840
TGGATAACGC AGAAGCGTGG AAGCAGGTCC GGGCATGCTG GCAGCCATGT GGGAGTTTCT 900
GGGCAGATGT GGTGCTGAGT GCCGGCCTGG GGTGGCCTCG ATTCTCTCCC TGCAGCCTTT 960
GCAGTGGCCA TCCCTTCTCT CCCCAATCAC AGAGGAAGAA AAGGAGGCTC ATTTATGCCT 1020
TCAACTCTGT TCATCCGTCA ATTTGCTGAG TGCCTAGGAG GCCTGGCGCA TAAAATATCA 1080
AATAAGACAA AGACCTGCCC CAGCGGAGTT ACATCCTCAT GGGAGCAACA GTGAGTGAGC 1140
AAGATCCCCA GGCACGTGGG ACGCACCCGG GAGGAGGCAG ATGGGATGCC TGCCGGAGAG 1200
GATGTGGAGC TGTGGCTGCG GCTGCTTTGG GGCCCCCAGG TTTGATGATT CCCCAGGAAG 1260
AGTCACTGGG TCCAGCACAG AGCCACCCTC AGAGCTAAGC TACATTCAGC AAAAGGACGC 1320
AGAGCGAGAT CAGCCACGCG AAGAGGTGTC TGGGCTGTCC GGAGGGCCCC AGGCAGGAGC 1380
TTCTGGAGTC CTCACCAGGG AAGACGGACA GGACGGACTT AATTCTCCCC TAAACCAGCC 1440
GCAACACTGA ACCAGTGTGA CGTGTTCTGT ACCAGAGGAG CTCACTAGCA ACTCAGTGCC 1500
CAAGGGTTTA TTGGGAGCTG TTCACATAGG CACCTGATAC CCAGCACGTG GCCCAATTCC 1560
AGACTCGCAG CAGGAGGGAG AGCAGGCGTT CCGCATGAAA GCAGCTTACA GTGACACCAG 1620
CTGGTGCTGG GAAAACACCA GGTAGGACCT GGCAGCCAGT CCTGATAAAA ATGCAAACAT 1680
AATAGGCATA GAGAGAACCT TCCCATACCT CAGAGCATCT GCCTGGAACT TCCGAGAATC 1740
ATGGTGAAGG TTTGAAGAGA TGATCCGCAG AAGCCCTTGG CCAAGCGCTG GAACCCAGTA 1800
AGGGCTTGGT GGCTTTCAGG ACCTCTCAAG TCACCTCCCA GCCCACCCCG TCCCTCCACC 1860
ACCGTCTCCC ACCTGCATCT CCCCGGACTG CCTCCTATTT AACCCCTGCT CCCCTCCAGC 1920
CGCCTGCTCA GTCTGTCCTC ACAGCAGCTG TGGGATGCAT TTAAAAGGTC AGCGAGGGCC 1980
GGGCGCGGTG GCTCACGCCT GTAACCCCAG CACTTTGGGA GGCCAAGGTG GGCAGATCAC 2040
CTGATGTCAG GGGTTCGAGA GCAGCCTGGC CAACATGGCG ACATCCCATT TCTGCTAAAA 2100
ATACAAAAAT TAGCTGGGCA TGGTGGCAGA CACCTGTAAT CCCAGTTACT CAGGCTGAGG 2160
CAGGAGAATC ACTTGAACCA GGAGACAGAG GTTGCAGTGA GCTGAGATTG CGCCATGGCA 2220
CTCCATCCTG 2230
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