| Tag | Content |
|---|
EnhancerAtlas ID | HS068-02680 |
Organism | Homo sapiens |
Tissue/cell | GM18526 |
Coordinate | chr19:898220-899430 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RFX1 | MA0509.2 | chr19:898859-898875 | GGTTGCCATGGAAACT | + | 6.67 | | RFX1 | MA0509.2 | chr19:898859-898875 | GGTTGCCATGGAAACT | - | 6.69 | | RFX2 | MA0600.2 | chr19:898859-898875 | GGTTGCCATGGAAACT | - | 7.06 | | RFX2 | MA0600.2 | chr19:898859-898875 | GGTTGCCATGGAAACT | + | 7.17 | | RFX5 | MA0510.2 | chr19:898859-898875 | GGTTGCCATGGAAACT | + | 7.06 | | RFX5 | MA0510.2 | chr19:898859-898875 | GGTTGCCATGGAAACT | - | 7.1 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_10779 | chr19:898304-899491 | CD19_Primary |
|
| | 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 |
| GH19I000898 | chr19 | 898420 | 899325 |
|
Enhancer Sequence | AAAAAAAAAA TATATATATA TATATATACA AAAAATTAGC AGGGCGTGGT GGCGGGCACC 60
TGTAGTCCCA GCTACTCGGG AGGCTGAGGC AGGAGAATGG CGTGAACCCG GGAGGTGGAG 120
CTTGCAGTGA GCTGAGATCG CGCCACTGCA CTCCAGCATG GGTGACAGAG CGAGACTTGG 180
TCTCAAAAAA AAAAAAAAAA AAGAAACCCG TCTCTACTAA AAATACAAAA TTAGCCGGGC 240
GTGCTGGCCG GCACCTGGGA TCCCAGCTAC TCGGGAGGCT GAGGCAGGAG AATCGCTTGA 300
ACCCGGAGGT GGAGGTTGCA GTGAGTAAAG ATTACGCCAC TGCACTCCAG CCTGGGTGGC 360
AGAATGAGAC TGTCTCAAAA AAACCAAACC TAACCAACCA AAACAAAAAA AAAGAGCCAC 420
GTCCCATGTG AGCTCCGCGC CTCAGCAGTC CCCTCTGCCT GGGACCCCCC CGTCCTCTAC 480
TCCCCATCTT GCTGGGACCC CTCCTCTTCC GTGTCAGGAC CACAGCTCCA CACCCACCAA 540
GCTCCAAGCC CCGCACCCCC AGCCAAGGCC GGATGTTCTG AGCAGAGGCA GGCATGGGGG 600
CTGCGTCTCC CACAGAGGGA ACAGAGGGAG GCATCGTCCG GTTGCCATGG AAACTGTCAC 660
CTCGGCAACT CCAGGCGGGG CGGCAGAGAC AGGTGTGAGA GGCTCAGGAC CAGATGGGGT 720
GCCTGGGGCC GGCGGCGCCT GCACAGACGT TCACTACGGG GGTGAGTTCT GAGACTGCGC 780
CCCGTTGGAA AAGTGGAGCG CAGGGGCCAG TAGGGGGTCT CGCCTGAGGT CCCACGTGTG 840
GTATGTGGGA GGCCTTAGAG TTAAATGCAA ACCTTCCAGA CACTGCGTCC CCCCATCTTA 900
TCTCTGGCTC TGGGAGGTCC CTCAAATCCA GGCTTCATCA CCCCCACCCC GGGCCCCGAA 960
GATGCAGATG GAGGAGTGTC TGTGTCCAGC AGCCTGGTTG TGTCTGCGGT CACCCTGCGT 1020
GGGGCCGCAT ATGCAGGGAG CTTCTGGTGA ATTCAAGGCA GGGTCCCACT GCCACCCCTG 1080
AGTTCGTAGC GTCCCCACTC CAGCCCCCTT CCCCACCTCC CCACCAAGCC CCACTCTGAG 1140
GAACCAGGCC CCTGGGACCC TGGCCACTTT CCCAGGTTGA GCTGGCCAAC TTGGGGTCTT 1200
GGGGGCCACC 1210
|
