| Tag | Content |
|---|
EnhancerAtlas ID | HS133-15845 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr19:46312590-46313860 |
Target genes | | Number: 23 | Name | Ensembl ID |
|
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CEBPA | MA0102.3 | chr19:46313751-46313762 | GATTGTGCAAT | - | 6.32 | | 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 |
|
| | 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 | CTCGCTCTGT CGCCCAGGCT GGAGTGTAGT GGTGCGACCT CCCCTCACTG CAATGTCCAC 60
CTCCCAGTTT CACGCCATTC TCCTGCCTCA GCCTCCCTAG TAGCTGGGAC TACAGGTGCC 120
CGCCACCATG CCCGGCTAAT TTTTTGTATT CTTAGTAGAG ACAGGGTTTC ACTTAGCCAG 180
GATGGTCTTG ATCTCCTGAC CTCGTGAACC ACCCGCCTCA GCCTCCCAAA GTGCTGGGAT 240
TACAGGCGTG AGCCACCGTG CCCGGCTAGT CAAAACTTTT CAAAACAGAG GTTCAGTGAT 300
GGGGAGAATT ATGCTACCAA AACAGCAACA CCTGCCGTGC AGCTGCTGTC AGCAGTAAAC 360
AGGAGAGTCC TAGAGCAGGA AGCCATCCAC AGAGCAAAGG CCGGGAGCAG AGACTCCTGC 420
AGGACCCTGT GTGGGGAGCA GATGGTGCAG GTGGCATTTC AAAGCAGTGG GGGGGCAGGA 480
AGGAATGGTT TATTGCATAA ATGCCATTCA AGGTCCTGGC TAGCCGTCTG GAAGACAGAA 540
AACGAGAGAA ATAAGAGCCT TGCCTTGACA GAAAAAGAAA CACAAAATGC TGAATCATGC 600
ATTTTTTATG AGTCATTTCC TAGAAGCATG TACAGGCCAC AAAAGCCCCC AGTTTTGCCC 660
TTCCACAGAC CCCACATTAA GAACTCCAGC TCTTGGCTGG GAGTGGTGGC TCACGCCTGT 720
AATCCTAATA CTTTGGGAGG CCGAGGCAGG AGGATGGCTT GAGGCCAAGA GTTCAAGACC 780
AACCCGGCCA ACATAGCAAG ACCCCCATCT CAATTATTTT TATTTATTTA TTTATTTTTA 840
TTTATTTATT TTTTTGAGAC AGAGTCTCGC TCTGTTGCCC AGGCTGGAGT GCAGTGGTGT 900
GATCTCGGCT CACTGCCAAG CTCCGCCTCC TGGGTTCATG CCATTCTCCT GCCTCAGCCT 960
CCGGAGTAGC TGGGACTGCA TGTGCCTGCT GCCACGCTTG GCTAATTTCT TATATTTTTA 1020
GTAGAGACGG GGTTTCATCA TGTTAGCAAA GATGGTCTTG ATCTCCTGAC CTCGTGATCT 1080
GCCCACCTCG GCCTCCCAAA GTGCTGAGGT TACAGATGTA AGCCACCCCA TCCTGCCAAG 1140
ACTGAAGTTG TTTTGTGACT GGATTGTGCA ATGCTGTCTT TCGCCTCCAG GCCTTGGCAC 1200
AGGCTGTGCC CTAAGTATGC TTGGGCCCCC ACTGACCCTG ATGCCCACCT CTCCTGACTG 1260
GCTCACTCAC 1270
|
