| Tag | Content |
|---|
EnhancerAtlas ID | HS037-11097 |
Organism | Homo sapiens |
Tissue/cell | ESC |
Coordinate | chr13:113545200-113546630 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr13:113545264-113545285 | GGAGGAGGGGGTGAGGGAGGG | + | 8.6 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_65270 | chr13:113544418-113546742 | 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 |
| GH13I112893 | chr13 | 113545401 | 113545550 | | GH13I112891 | chr13 | 113545702 | 113546621 |
|
Enhancer Sequence | CCCATGAGGC CGAGCCCGAC GGCACCTGGG CAGTGAGAAG CCAAGACCTC GGCACTTTCG 60
TTCTGGAGGA GGGGGTGAGG GAGGGACAGT ACCGCTGTCT TGTCTAGGCA GGGTTTGTGC 120
AGATTTGGGG GCTGGAGGAG GCCAGCGTAG CCCTGCCCTG CTCCCTCCAG CCACCCAGAA 180
CTGCAGAGGC GCCAGGCCCA AGTCTGCCTG TGGCGTGTCC AACACAGAAG GGCAGATTCC 240
GAGACAAACC AGGGTGGCTA CAGGTTTACA AGGGGGCCCT GTGGTCTTTC CTCTGTAGGT 300
GGGAGGACAC TGTCGCCACC TTCCTCGGCT GTGTAAGGCG AGCACAAAGG AGTCTCCCAC 360
CTGAGATACG ATCACTCCTT TTCTTTCCCG TACAGACATC TCTGTGGGAG CGATGCTTTC 420
ACATAAAGCG CTTAATCTCC AATGGTAAAG TTTCCAACAC TAAGTCGAGA CGTTGGAACA 480
ATTTGGAAGC AGATGAACCT TCCTAAACTG CTTATGGGAC ACAGTGACCA CACGGAGATG 540
CCCTGGAAGG ATTCCAGCCT TTGGGGTCAC AGGCACGGGC ACCACAGCTT CCCGGGTGCC 600
TGCTACCTGA GCTCGCTGTA AGTGCCGCAC GGCTTACGTG GAATCCACAG AGGCAGCCCG 660
TACTCCCCCC TCCATGTGCA GCGCCCAGAC ACGTGTGCCG AGGCTGCAGG TGTGCTACAG 720
TGCGGCGGCC AACCGGCTTT CCCCTGCAGC CTCAGCTCCT GCGGGATCTG CTCACTGGTA 780
GGCAGTGACG CCCTGGCGGG AGTTGTCCCT GAGGTCTCTG CTCCTCCTGC TGTGCTCGCA 840
GGGGAACCTG TTTGTGACGT AGTCTCCTTG TGCCCCACTG GGCTTCTGAG GCTGTGAAAG 900
CTGGTGGAGC ACAAAGGGCT TGCCCGGCCC TAACAAGCCT GGCCCCAGCA GGGCACCGCG 960
GGCAGCCTCT GATGCGCGGC TCTGGGCCTT TGTCCTCGGC TGAATTAATT TCCTCTTGAA 1020
TTGCCTCAAC TTTAGAATGA GCCCTAGCCT TTTCTGAAGC ACACACATCT TGGGGTTTTG 1080
TCCTCTGTAT TTTCGCTGCA TTGGCTGCCA ATGCGGAAAG CTTTCATGGA GAAGACGTTC 1140
TGGCTTCTTG TCTGTCTGTC CCCTGAGGGC TGCGGGCCAG CTCCATGCCC GTCCACGGTG 1200
TGCAGGTGGA GGCATCTTTC AGGGTATCAG GTGGGAATCC GTGCTTCCTG GCAAAGTCTG 1260
TTCCAGTGTG GTGCCCACTG TCCATGCGCC TGTGGGTGTG AGCCTGCACC CTGCACGAAT 1320
GTGTGGAGCG GGGTCGTGGC TGGCTGGGGT CACTGCCTGT CCCCTCCTTT TCCGCAGCCA 1380
CGGTGCCATC TGCTTGCACG TCCTGCAGGA GATCCTCAGG GCGGGTTCCC 1430
|
