| Tag | Content |
|---|
EnhancerAtlas ID | HS080-17540 |
Organism | Homo sapiens |
Tissue/cell | H9 |
Coordinate | chr19:45639190-45640610 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| TP53 | MA0106.3 | chr19:45639717-45639735 | GGCATGCATGGGCTTGTC | + | 6.16 | | TP53 | MA0106.3 | chr19:45639717-45639735 | GGCATGCATGGGCTTGTC | - | 6.22 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_65319 | chr19:45639385-45642487 | 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 |
| GH19I045136 | chr19 | 45639563 | 45641967 |
|
Enhancer Sequence | CCACCACACC CAGCTAATTT TTGTATTTTT AGTAGAGGCT GAGTTTCGCC GTGTTGCCCC 60
GGCTGGTCTT GAAATCCTGA CCTCAAGTGA TCCGTCCACC TCAGCCTTCC AAAGTGCTGG 120
GATTACAGGC ATGAGCCACC ATGCCTGGCC TGGAATGATG ATTTTTAAGG CGAAACATTA 180
AATAGGATTG CAAAGGATGC CAGTTGGAAT ATCATTAGCT AAATGCTCTT CCTCACTGAA 240
TTGACATGTG AAGCGATAGG ATGTAGCAGC AGCTGTAATA AGGCCTTCAG TCTCAGAGTA 300
GTGATGGGCA TTCAGAATCT GCAGTAACTT GATGCAATGG GAAAATATCT GTCGTTTCTT 360
TTCATGTCAG TCTCAAGGTC TGCTAAACAC TGTTTCTTTT CTCTCTCTCT TTTGGCCTCT 420
GTTAATAAGA AGGAAATGCT AAATTTCAGT TCCATTCATG AAAATAAAGA GATAAGTGTC 480
TCCCCTCAAG TTCGTGGGCC CTTTGGGGGT CAAATGGTTA AGACCAGGGC ATGCATGGGC 540
TTGTCCATGG CTTGGGGTAG CTGCTGCAGT CCTGGGGGCT GCCTTCCCAG GCAGGGCAAG 600
CTCCGGTCCC CACTAGAGCT CCAGGGTCAC CAAGCACATG GGCCTTTGTC AGACAGCTCC 660
CTTTCTGTCT GCAAGAGGGG CACCTGCCAT CAGCTGATCC CCTGCAGCTC CTCCCAGGCC 720
TCCACCCCCA AGGAGGAGGA AGTGCTCAGG CAGGGACCAG GCCTGACCTC TGGGGAGGCT 780
GGCGGCTGGC CTCTGTCGGC TTCTTTCCTC CAGCACCGCA GTTCAGCAAC CCACCGCCAC 840
CCAGCACAGT GGCCAGAGCG GAGTCCCAGG GTCTGATGTT AGACTCTGCT CTGGACCAGC 900
CACCTGGTCC CAGGGAGACA CCATACTTTA CCCAGACCTC AGCTTCTTCC CCTAGAAAAT 960
GGGGCAGTGC TTGATGAGAC CAGGGGTCCA GAGCCCCTGG CCTAGCAGGG TGGCAGGAGG 1020
AGGAGTCCAC ACGGAGATAT TACTGGACTG GGAGCTCTCT CAGGGACTCC CACTGCGTCC 1080
AGCAGCAGCG GATTGGCAGC AGGGCGAGGG GCCCCCCCCC CAAGAAGCTG CCAGCAAGCC 1140
CTCTTCCTGG CCCCCTTCCC TGCCCATTGT GGCATCTCCA TGCCCAATAT CTGCTGGCCC 1200
GAAGATCTTT CTAACGGCCA GTCCTGACCT CTCCCTCTTC TGCTCCTAGC CTTTCCTTCC 1260
TGCTCCGCTG GTCACCCTGA GGTAAAATCC AAGCTCTAAT AGCCAAAAAC TGGAAACAGT 1320
ACAAATTCCT GTCAGCTGGT GAATGGGCAA ACACAACGCA GCACATCCTA TAATTACTCT 1380
TCAGCAGTAT AAAGGGACTG AAACTCACGC TCATTATGCT 1420
|
