| Tag | Content |
|---|
EnhancerAtlas ID | HS049-03087 |
Organism | Homo sapiens |
Tissue/cell | Fetal_spinal_cord |
Coordinate | chr16:87957730-87959260 |
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 | CCAAGATCTG GTTGTCCCAC TTTCCCTCTT CTTCTCCGAG CTGGTCTTGT CCTTCCAAGA 60
AGTTGCACTT TGCTTACGTT GGCTGGAGTT GGGGTTACTG CTGCTGGCAC TCAGCAAGCC 120
CCACACGGGA AGCATCCGCG GGGGTTGCAG TGGAGCCTGA TGAAGCAACC GTGAATGGCA 180
CTGAGCATAC AGGCAGCGTG GCTCCTTCTC ACCTTCGAAA GGAGAGAGAG ACACTGGAAG 240
GACCAAGCCG TGGTGTTTGC GATGCACTGT GTAGGGCCTG GCACAGAGAA GAAGCTCTCA 300
CGCCCTGCCC CCAACAGCAG GTGCATTAGA GGCAGGAGCA GGCTCAGGCT GGGCCTCTAC 360
TCTCCATGGG GTGCCTCTCC CCGGGCTCCA GGAAGGCCTG CACATACGGC TCAGCGCACT 420
CATCCGTGGG CACCGTGCCT GCTCACTGAG GTCCCCTGTG TTGAGAATTT CTAGGCATAT 480
GCAGATTTAA GTGGCTGAAA TGCAAGCACC ATGTCATGAC GAAGCTGGGA CGCAGCTGGG 540
CAGACCTCCC CGTGACAGCA GGAGCTGGGG AAGCCCCGGT GAGCATGTTT AGTGTAAGGA 600
AGGTGAATGC TGCCTCCGCA TGCACAGCGA GAGGGCATGA AGGTGAGCGT GGGGGCAGCG 660
TCCCGCTTGT TGGTCCCGCT TGGATAACGC AGAAGCGTGG AAGCAGGTCC GGGCATGCTG 720
GCAGCCATGT GGGAGTTTCT GGGCAGATGT GGTGCTGAGT GCCGGCCTGG GGTGGCCTCG 780
ATTCTCTCCC TGCAGCCTTT GCAGTGGCCA TCCCTTCTCT CCCCAATCAC AGAGGAAGAA 840
AAGGAGGCTC ATTTATGCCT TCAACTCTGT TCATCCGTCA ATTTGCTGAG TGCCTAGGAG 900
GCCTGGCGCA TAAAATATCA AATAAGACAA AGACCTGCCC CAGCGGAGTT ACATCCTCAT 960
GGGAGCAACA GTGAGTGAGC AAGATCCCCA GGCACGTGGG ACGCACCCGG GAGGAGGCAG 1020
ATGGGATGCC TGCCGGAGAG GATGTGGAGC TGTGGCTGCG GCTGCTTTGG GGCCCCCAGG 1080
TTTGATGATT CCCCAGGAAG AGTCACTGGG TCCAGCACAG AGCCACCCTC AGAGCTAAGC 1140
TACATTCAGC AAAAGGACGC AGAGCGAGAT CAGCCACGCG AAGAGGTGTC TGGGCTGTCC 1200
GGAGGGCCCC AGGCAGGAGC TTCTGGAGTC CTCACCAGGG AAGACGGACA GGACGGACTT 1260
AATTCTCCCC TAAACCAGCC GCAACACTGA ACCAGTGTGA CGTGTTCTGT ACCAGAGGAG 1320
CTCACTAGCA ACTCAGTGCC CAAGGGTTTA TTGGGAGCTG TTCACATAGG CACCTGATAC 1380
CCAGCACGTG GCCCAATTCC AGACTCGCAG CAGGAGGGAG AGCAGGCGTT CCGCATGAAA 1440
GCAGCTTACA GTGACACCAG CTGGTGCTGG GAAAACACCA GGTAGGACCT GGCAGCCAGT 1500
CCTGATAAAA ATGCAAACAT AATAGGCATA 1530
|
