| Tag | Content |
|---|
EnhancerAtlas ID | HS098-21114 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr16:4992890-4994230 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOSL1 | MA0477.1 | chr16:4993498-4993509 | AGTGACTCATC | + | 6.02 | | JUND | MA0491.1 | chr16:4993498-4993509 | AGTGACTCATC | + | 6.32 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_26593 | chr16:4991884-4996691 | Esophagus | | SE_65358 | chr16:4991965-4999969 | Pancreatic_islets |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH16I004942 | chr16 | 4992177 | 4996570 |
|
Enhancer Sequence | GGGACTACAG ATGCACACCA GGAAGCCTGG GTAATTTTTA AATTTTTTGT AAATACGGGG 60
TCTTGCTGTT GCCCAGGCTG GTTGAGAACT CCTGGGCTCA AGTGATCCTC CCACCTTGGC 120
CTTCCAAACT GCTGGGAATA CAGGCATGGG CCACGGTGCC TGGCCTCTCT TGTCTTACTT 180
TTCAGGGAAG GAAATGGGCC CTGAGAAGCA CAGGGCCCAT TTGGGCTGGT ACCTGGGTCA 240
GCCTGCTCCT GGACTGAGCT CTTGAACCTC TGCCTCCCTC CACTCTTCAG AGTTCTAATT 300
CCTGGGCTCG GGCTTGGGGC AGCTGGGCTG GTCTCCCGCT GACTCAGCTG AGCCTGGCCC 360
AGGAGTGGCG GGTAGAATTA GCAGATTTAG GGAGGAATTT GAGTGGCGCT TCACCATCCC 420
TCCCCTCTCC ATTCTCTAGG AGCTGGGCTA GGAGCTCCCA TGGCTGTGTG TGTGCGCACA 480
TGTGTACACA CGTGCACACA CCACACGTTT GTGGGCAGGC CGGATGGGGT GGGAGATCCG 540
TTCTCACCCC ATGCATCCTC CTCTGGGCAG ATGGGATTTG TTTGGATCCG CGAAGCCCTC 600
TCCTGCCAAG TGACTCATCC CCTCTGTTGC CGTGGGTGGA GGGCCAGCCT GCCGGGGTGG 660
GGGAGGGTGC TTGCTTTCCT CGAGTTTGCT CGCACCTTCA GGGCCATTTG TTCCCTGGCA 720
ACCAGGCCAC CCTCAGCGAC CCTGAAACCT GTGTTCCTGC AGCCAGACCA GGCAGCCAGC 780
TCATGGGAGG CCACCAACTT CGGAAGGGTT CCTCACGCCC GCCCTCCTTG TTTGCCATCA 840
CTGTTGCCCT AGCAGCTGGA GAGGTGTTTG GGGTATTCGC CTGTGAACCA GTTTGAAACA 900
AGAGGGGCAG CATTCGCCCA GCCCGGGACA GAGGGACATG TGGGATATAT CCCGAGCCCT 960
CTCCGAGACA GCCATTCTCC CATCTGTGGC TGTATGCACC CCAACTTGGG GTGCATTTAC 1020
AAATGCAGAT TCCAGGGTCC CTCCCTGGAA GAGATTACGG TTGGGTGAGT CTTGGCAGGG 1080
CCGAGAAATC TGCATTTATT TATTTATTAA TTATAGAGAT GAGGTCTCGC TGTGTTACCC 1140
AGGCTGGTCT TGAATGCCTG GGCTCAAGTC AATCTCTTGC CTCAGCCTCC CAAAGTGCTG 1200
GGATTACAGG CATGAGCCAC CAAGGAATCT GCATTTTTTT TGAGACAGGG TCTGACTCTC 1260
TTGCCTAAAC TGGAGTGCAG TGGTACAATC TCGGCTCACT GCAACATCCG CCTCCCAAGC 1320
TCAAGCAGTT CCCCTGCCTC 1340
|
