| Tag | Content |
|---|
EnhancerAtlas ID | HS182-11488 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr19:45639290-45641070 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Myog | MA0500.1 | chr19:45640751-45640762 | CTGCAGCTGTT | - | 6.02 | | TP53 | MA0106.3 | chr19:45639717-45639735 | GGCATGCATGGGCTTGTC | + | 6.16 | | TP53 | MA0106.3 | chr19:45639717-45639735 | GGCATGCATGGGCTTGTC | - | 6.22 | | Tcf12 | MA0521.1 | chr19:45640751-45640762 | CTGCAGCTGTT | - | 6.62 |
|
| | 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: 2 | Chromosome | Start | End |
| chr19 | 45639410 | 45640200 | | chr19 | 45639425 | 45641049 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH19I045136 | chr19 | 45639563 | 45641967 |
|
Enhancer Sequence | TCAGCCTTCC AAAGTGCTGG GATTACAGGC ATGAGCCACC ATGCCTGGCC TGGAATGATG 60
ATTTTTAAGG CGAAACATTA AATAGGATTG CAAAGGATGC CAGTTGGAAT ATCATTAGCT 120
AAATGCTCTT CCTCACTGAA TTGACATGTG AAGCGATAGG ATGTAGCAGC AGCTGTAATA 180
AGGCCTTCAG TCTCAGAGTA GTGATGGGCA TTCAGAATCT GCAGTAACTT GATGCAATGG 240
GAAAATATCT GTCGTTTCTT TTCATGTCAG TCTCAAGGTC TGCTAAACAC TGTTTCTTTT 300
CTCTCTCTCT TTTGGCCTCT GTTAATAAGA AGGAAATGCT AAATTTCAGT TCCATTCATG 360
AAAATAAAGA GATAAGTGTC TCCCCTCAAG TTCGTGGGCC CTTTGGGGGT CAAATGGTTA 420
AGACCAGGGC ATGCATGGGC TTGTCCATGG CTTGGGGTAG CTGCTGCAGT CCTGGGGGCT 480
GCCTTCCCAG GCAGGGCAAG CTCCGGTCCC CACTAGAGCT CCAGGGTCAC CAAGCACATG 540
GGCCTTTGTC AGACAGCTCC CTTTCTGTCT GCAAGAGGGG CACCTGCCAT CAGCTGATCC 600
CCTGCAGCTC CTCCCAGGCC TCCACCCCCA AGGAGGAGGA AGTGCTCAGG CAGGGACCAG 660
GCCTGACCTC TGGGGAGGCT GGCGGCTGGC CTCTGTCGGC TTCTTTCCTC CAGCACCGCA 720
GTTCAGCAAC CCACCGCCAC CCAGCACAGT GGCCAGAGCG GAGTCCCAGG GTCTGATGTT 780
AGACTCTGCT CTGGACCAGC CACCTGGTCC CAGGGAGACA CCATACTTTA CCCAGACCTC 840
AGCTTCTTCC CCTAGAAAAT GGGGCAGTGC TTGATGAGAC CAGGGGTCCA GAGCCCCTGG 900
CCTAGCAGGG TGGCAGGAGG AGGAGTCCAC ACGGAGATAT TACTGGACTG GGAGCTCTCT 960
CAGGGACTCC CACTGCGTCC AGCAGCAGCG GATTGGCAGC AGGGCGAGGG GCCCCCCCCC 1020
CAAGAAGCTG CCAGCAAGCC CTCTTCCTGG CCCCCTTCCC TGCCCATTGT GGCATCTCCA 1080
TGCCCAATAT CTGCTGGCCC GAAGATCTTT CTAACGGCCA GTCCTGACCT CTCCCTCTTC 1140
TGCTCCTAGC CTTTCCTTCC TGCTCCGCTG GTCACCCTGA GGTAAAATCC AAGCTCTAAT 1200
AGCCAAAAAC TGGAAACAGT ACAAATTCCT GTCAGCTGGT GAATGGGCAA ACACAACGCA 1260
GCACATCCTA TAATTACTCT TCAGCAGTAT AAAGGGACTG AAACTCACGC TCATTATGCT 1320
CAGTAAGAGA AGCCAACCGC AGAAGGCCAC ACAGTTTCAA TTCCATTTTA ATGAAATGTC 1380
CAGAAAAGGC AAATCTGTGT AGATAGAAAG CCCAGCCCTC CCTTCCGCAT GGTGGCGGCT 1440
GTGGCCCTCC AGGGACCGGG GCTGCAGCTG TTGGGTTTGG GCTACGTCCC TTCATTCATG 1500
CTGGGAGCCA CTGCCTGTTA GCCTGGGAAC ACCCGGGACC AGGCCTGTCT CTTCCAACTG 1560
CTTCTGTGTC CTGCGTCAAG GGGCCGGGCC CTGAATAGCG TACGGCGATG TTTAGCTGTT 1620
GAGAGTGTTT TGGGAGTGGG GATCCTGAGA GGCACGTGGC ATTGTAGTTG AGAGCTGAGT 1680
TCAAAGCCCG GCTCGCATAT ATACCAGGTG TGTGATCTTG GGCAAGGTTG TTTCTCTGAG 1740
CTTGGTTTCC TCATAGGGTT GAAGTGAGGA TTCATTCTTT 1780
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