| Tag | Content |
|---|
EnhancerAtlas ID | HS095-11876 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr16:87957930-87959380 |
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 | GCTCCTTCTC ACCTTCGAAA GGAGAGAGAG ACACTGGAAG GACCAAGCCG TGGTGTTTGC 60
GATGCACTGT GTAGGGCCTG GCACAGAGAA GAAGCTCTCA CGCCCTGCCC CCAACAGCAG 120
GTGCATTAGA GGCAGGAGCA GGCTCAGGCT GGGCCTCTAC TCTCCATGGG GTGCCTCTCC 180
CCGGGCTCCA GGAAGGCCTG CACATACGGC TCAGCGCACT CATCCGTGGG CACCGTGCCT 240
GCTCACTGAG GTCCCCTGTG TTGAGAATTT CTAGGCATAT GCAGATTTAA GTGGCTGAAA 300
TGCAAGCACC ATGTCATGAC GAAGCTGGGA CGCAGCTGGG CAGACCTCCC CGTGACAGCA 360
GGAGCTGGGG AAGCCCCGGT GAGCATGTTT AGTGTAAGGA AGGTGAATGC TGCCTCCGCA 420
TGCACAGCGA GAGGGCATGA AGGTGAGCGT GGGGGCAGCG TCCCGCTTGT TGGTCCCGCT 480
TGGATAACGC AGAAGCGTGG AAGCAGGTCC GGGCATGCTG GCAGCCATGT GGGAGTTTCT 540
GGGCAGATGT GGTGCTGAGT GCCGGCCTGG GGTGGCCTCG ATTCTCTCCC TGCAGCCTTT 600
GCAGTGGCCA TCCCTTCTCT CCCCAATCAC AGAGGAAGAA AAGGAGGCTC ATTTATGCCT 660
TCAACTCTGT TCATCCGTCA ATTTGCTGAG TGCCTAGGAG GCCTGGCGCA TAAAATATCA 720
AATAAGACAA AGACCTGCCC CAGCGGAGTT ACATCCTCAT GGGAGCAACA GTGAGTGAGC 780
AAGATCCCCA GGCACGTGGG ACGCACCCGG GAGGAGGCAG ATGGGATGCC TGCCGGAGAG 840
GATGTGGAGC TGTGGCTGCG GCTGCTTTGG GGCCCCCAGG TTTGATGATT CCCCAGGAAG 900
AGTCACTGGG TCCAGCACAG AGCCACCCTC AGAGCTAAGC TACATTCAGC AAAAGGACGC 960
AGAGCGAGAT CAGCCACGCG AAGAGGTGTC TGGGCTGTCC GGAGGGCCCC AGGCAGGAGC 1020
TTCTGGAGTC CTCACCAGGG AAGACGGACA GGACGGACTT AATTCTCCCC TAAACCAGCC 1080
GCAACACTGA ACCAGTGTGA CGTGTTCTGT ACCAGAGGAG CTCACTAGCA ACTCAGTGCC 1140
CAAGGGTTTA TTGGGAGCTG TTCACATAGG CACCTGATAC CCAGCACGTG GCCCAATTCC 1200
AGACTCGCAG CAGGAGGGAG AGCAGGCGTT CCGCATGAAA GCAGCTTACA GTGACACCAG 1260
CTGGTGCTGG GAAAACACCA GGTAGGACCT GGCAGCCAGT CCTGATAAAA ATGCAAACAT 1320
AATAGGCATA GAGAGAACCT TCCCATACCT CAGAGCATCT GCCTGGAACT TCCGAGAATC 1380
ATGGTGAAGG TTTGAAGAGA TGATCCGCAG AAGCCCTTGG CCAAGCGCTG GAACCCAGTA 1440
AGGGCTTGGT 1450
|
