| Tag | Content |
|---|
EnhancerAtlas ID | HS044-05448 |
Organism | Homo sapiens |
Tissue/cell | Fetal_kidney |
Coordinate | chr16:87957760-87959570 |
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 | CTTCTCCGAG CTGGTCTTGT CCTTCCAAGA AGTTGCACTT TGCTTACGTT GGCTGGAGTT 60
GGGGTTACTG CTGCTGGCAC TCAGCAAGCC CCACACGGGA AGCATCCGCG GGGGTTGCAG 120
TGGAGCCTGA TGAAGCAACC GTGAATGGCA CTGAGCATAC AGGCAGCGTG GCTCCTTCTC 180
ACCTTCGAAA GGAGAGAGAG ACACTGGAAG GACCAAGCCG TGGTGTTTGC GATGCACTGT 240
GTAGGGCCTG GCACAGAGAA GAAGCTCTCA CGCCCTGCCC CCAACAGCAG GTGCATTAGA 300
GGCAGGAGCA GGCTCAGGCT GGGCCTCTAC TCTCCATGGG GTGCCTCTCC CCGGGCTCCA 360
GGAAGGCCTG CACATACGGC TCAGCGCACT CATCCGTGGG CACCGTGCCT GCTCACTGAG 420
GTCCCCTGTG TTGAGAATTT CTAGGCATAT GCAGATTTAA GTGGCTGAAA TGCAAGCACC 480
ATGTCATGAC GAAGCTGGGA CGCAGCTGGG CAGACCTCCC CGTGACAGCA GGAGCTGGGG 540
AAGCCCCGGT GAGCATGTTT AGTGTAAGGA AGGTGAATGC TGCCTCCGCA TGCACAGCGA 600
GAGGGCATGA AGGTGAGCGT GGGGGCAGCG TCCCGCTTGT TGGTCCCGCT TGGATAACGC 660
AGAAGCGTGG AAGCAGGTCC GGGCATGCTG GCAGCCATGT GGGAGTTTCT GGGCAGATGT 720
GGTGCTGAGT GCCGGCCTGG GGTGGCCTCG ATTCTCTCCC TGCAGCCTTT GCAGTGGCCA 780
TCCCTTCTCT CCCCAATCAC AGAGGAAGAA AAGGAGGCTC ATTTATGCCT TCAACTCTGT 840
TCATCCGTCA ATTTGCTGAG TGCCTAGGAG GCCTGGCGCA TAAAATATCA AATAAGACAA 900
AGACCTGCCC CAGCGGAGTT ACATCCTCAT GGGAGCAACA GTGAGTGAGC AAGATCCCCA 960
GGCACGTGGG ACGCACCCGG GAGGAGGCAG ATGGGATGCC TGCCGGAGAG GATGTGGAGC 1020
TGTGGCTGCG GCTGCTTTGG GGCCCCCAGG TTTGATGATT CCCCAGGAAG AGTCACTGGG 1080
TCCAGCACAG AGCCACCCTC AGAGCTAAGC TACATTCAGC AAAAGGACGC AGAGCGAGAT 1140
CAGCCACGCG AAGAGGTGTC TGGGCTGTCC GGAGGGCCCC AGGCAGGAGC TTCTGGAGTC 1200
CTCACCAGGG AAGACGGACA GGACGGACTT AATTCTCCCC TAAACCAGCC GCAACACTGA 1260
ACCAGTGTGA CGTGTTCTGT ACCAGAGGAG CTCACTAGCA ACTCAGTGCC CAAGGGTTTA 1320
TTGGGAGCTG TTCACATAGG CACCTGATAC CCAGCACGTG GCCCAATTCC AGACTCGCAG 1380
CAGGAGGGAG AGCAGGCGTT CCGCATGAAA GCAGCTTACA GTGACACCAG CTGGTGCTGG 1440
GAAAACACCA GGTAGGACCT GGCAGCCAGT CCTGATAAAA ATGCAAACAT AATAGGCATA 1500
GAGAGAACCT TCCCATACCT CAGAGCATCT GCCTGGAACT TCCGAGAATC ATGGTGAAGG 1560
TTTGAAGAGA TGATCCGCAG AAGCCCTTGG CCAAGCGCTG GAACCCAGTA AGGGCTTGGT 1620
GGCTTTCAGG ACCTCTCAAG TCACCTCCCA GCCCACCCCG TCCCTCCACC ACCGTCTCCC 1680
ACCTGCATCT CCCCGGACTG CCTCCTATTT AACCCCTGCT CCCCTCCAGC CGCCTGCTCA 1740
GTCTGTCCTC ACAGCAGCTG TGGGATGCAT TTAAAAGGTC AGCGAGGGCC GGGCGCGGTG 1800
GCTCACGCCT 1810
|
