| Tag | Content |
|---|
EnhancerAtlas ID | HS051-13285 |
Organism | Homo sapiens |
Tissue/cell | Fetal_thymus |
Coordinate | chr19:898410-899430 |
Target genes | | Number: 32 | Name | Ensembl ID |
|
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 AAGAAACCCG TCTCTACTAA AAATACAAAA TTAGCCGGGC GTGCTGGCCG 60
GCACCTGGGA TCCCAGCTAC TCGGGAGGCT GAGGCAGGAG AATCGCTTGA ACCCGGAGGT 120
GGAGGTTGCA GTGAGTAAAG ATTACGCCAC TGCACTCCAG CCTGGGTGGC AGAATGAGAC 180
TGTCTCAAAA AAACCAAACC TAACCAACCA AAACAAAAAA AAAGAGCCAC GTCCCATGTG 240
AGCTCCGCGC CTCAGCAGTC CCCTCTGCCT GGGACCCCCC CGTCCTCTAC TCCCCATCTT 300
GCTGGGACCC CTCCTCTTCC GTGTCAGGAC CACAGCTCCA CACCCACCAA GCTCCAAGCC 360
CCGCACCCCC AGCCAAGGCC GGATGTTCTG AGCAGAGGCA GGCATGGGGG CTGCGTCTCC 420
CACAGAGGGA ACAGAGGGAG GCATCGTCCG GTTGCCATGG AAACTGTCAC CTCGGCAACT 480
CCAGGCGGGG CGGCAGAGAC AGGTGTGAGA GGCTCAGGAC CAGATGGGGT GCCTGGGGCC 540
GGCGGCGCCT GCACAGACGT TCACTACGGG GGTGAGTTCT GAGACTGCGC CCCGTTGGAA 600
AAGTGGAGCG CAGGGGCCAG TAGGGGGTCT CGCCTGAGGT CCCACGTGTG GTATGTGGGA 660
GGCCTTAGAG TTAAATGCAA ACCTTCCAGA CACTGCGTCC CCCCATCTTA TCTCTGGCTC 720
TGGGAGGTCC CTCAAATCCA GGCTTCATCA CCCCCACCCC GGGCCCCGAA GATGCAGATG 780
GAGGAGTGTC TGTGTCCAGC AGCCTGGTTG TGTCTGCGGT CACCCTGCGT GGGGCCGCAT 840
ATGCAGGGAG CTTCTGGTGA ATTCAAGGCA GGGTCCCACT GCCACCCCTG AGTTCGTAGC 900
GTCCCCACTC CAGCCCCCTT CCCCACCTCC CCACCAAGCC CCACTCTGAG GAACCAGGCC 960
CCTGGGACCC TGGCCACTTT CCCAGGTTGA GCTGGCCAAC TTGGGGTCTT GGGGGCCACC 1020
|
