| Tag | Content |
|---|
EnhancerAtlas ID | HS051-14430 |
Organism | Homo sapiens |
Tissue/cell | Fetal_thymus |
Coordinate | chr19:46312470-46313740 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Foxo1 | MA0480.1 | chr19:46312943-46312954 | AGTAAACAGGA | - | 6.32 | | JUN(var.2) | MA0489.1 | chr19:46313197-46313211 | ATGAGTCATTTCCT | - | 8.12 | | Stat4 | MA0518.1 | chr19:46313202-46313216 | TCATTTCCTAGAAG | - | 6.69 | | Zfx | MA0146.2 | chr19:46312502-46312516 | CCCGCCTCGGCCTC | + | 6.01 |
|
| | 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 |
| GH19I045809 | chr19 | 46312606 | 46314232 |
|
Enhancer Sequence | GGATGGTCTC GATCTCCTGA CCTCGTGATC CACCCGCCTC GGCCTCCCAA AGTGCTAGGA 60
TTACAGGTGT GAGCCACTGC GCCTGGCCTT TTTTTTTTTT TTTTTTTTTT GAGATGGAGT 120
CTCGCTCTGT CGCCCAGGCT GGAGTGTAGT GGTGCGACCT CCCCTCACTG CAATGTCCAC 180
CTCCCAGTTT CACGCCATTC TCCTGCCTCA GCCTCCCTAG TAGCTGGGAC TACAGGTGCC 240
CGCCACCATG CCCGGCTAAT TTTTTGTATT CTTAGTAGAG ACAGGGTTTC ACTTAGCCAG 300
GATGGTCTTG ATCTCCTGAC CTCGTGAACC ACCCGCCTCA GCCTCCCAAA GTGCTGGGAT 360
TACAGGCGTG AGCCACCGTG CCCGGCTAGT CAAAACTTTT CAAAACAGAG GTTCAGTGAT 420
GGGGAGAATT ATGCTACCAA AACAGCAACA CCTGCCGTGC AGCTGCTGTC AGCAGTAAAC 480
AGGAGAGTCC TAGAGCAGGA AGCCATCCAC AGAGCAAAGG CCGGGAGCAG AGACTCCTGC 540
AGGACCCTGT GTGGGGAGCA GATGGTGCAG GTGGCATTTC AAAGCAGTGG GGGGGCAGGA 600
AGGAATGGTT TATTGCATAA ATGCCATTCA AGGTCCTGGC TAGCCGTCTG GAAGACAGAA 660
AACGAGAGAA ATAAGAGCCT TGCCTTGACA GAAAAAGAAA CACAAAATGC TGAATCATGC 720
ATTTTTTATG AGTCATTTCC TAGAAGCATG TACAGGCCAC AAAAGCCCCC AGTTTTGCCC 780
TTCCACAGAC CCCACATTAA GAACTCCAGC TCTTGGCTGG GAGTGGTGGC TCACGCCTGT 840
AATCCTAATA CTTTGGGAGG CCGAGGCAGG AGGATGGCTT GAGGCCAAGA GTTCAAGACC 900
AACCCGGCCA ACATAGCAAG ACCCCCATCT CAATTATTTT TATTTATTTA TTTATTTTTA 960
TTTATTTATT TTTTTGAGAC AGAGTCTCGC TCTGTTGCCC AGGCTGGAGT GCAGTGGTGT 1020
GATCTCGGCT CACTGCCAAG CTCCGCCTCC TGGGTTCATG CCATTCTCCT GCCTCAGCCT 1080
CCGGAGTAGC TGGGACTGCA TGTGCCTGCT GCCACGCTTG GCTAATTTCT TATATTTTTA 1140
GTAGAGACGG GGTTTCATCA TGTTAGCAAA GATGGTCTTG ATCTCCTGAC CTCGTGATCT 1200
GCCCACCTCG GCCTCCCAAA GTGCTGAGGT TACAGATGTA AGCCACCCCA TCCTGCCAAG 1260
ACTGAAGTTG 1270
|
