| Tag | Content |
|---|
EnhancerAtlas ID | HS133-22349 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr3:52286970-52288410 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| SPI1 | MA0080.4 | chr3:52287400-52287414 | CACTTCCTCTTTCC | - | 6.1 |
|
| | Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
| SE_27410 | chr3:52286634-52288583 | Esophagus | | SE_42979 | chr3:52287050-52288450 | Lung | | SE_54049 | chr3:52286299-52288509 | Spleen |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr3 | 52287340 | 52287625 | | chr3 | 52287189 | 52288386 | | chr3 | 52287200 | 52288123 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH03I052251 | chr3 | 52285754 | 52289086 |
|
Enhancer Sequence | CTGCAACCTC TAGCCTCCTG GGTTCAAGTG ATTCTCCTGC CTCAGCCTCC TGAACAGTTG 60
GAATTACAGG CACACACCAC CACACCCAAT ATTTTTAGTA GAGATGGGGT TTCATCATGT 120
TGGCCAGCCT GGTCTCAAAC TCCTGACCTC AGGTGATCCA CCCACCTCGG TCTCCCAAAG 180
TGCTGGGATT ACAGGCGTGA GCCACTGCAC CCAGCCTCAG ACCCCCTTTC CTACCCATTA 240
ACTCTAGATT TCATTTCCTA CACATTCTCC AGGGAAGACT GGAAAAACTG CATCAGATAT 300
TTCCCACTGC TATATTCCAC AGTGCAGGAC TTCAGGGTTG AACCTGTCCA CAGCTAGGCC 360
CTATGGTAGT CTTGCTAGGA CTCCTCTAGC CAGGCAGCTT GAGTGCTGTC CTACCAGCCT 420
GTAGGAGTGT CACTTCCTCT TTCCTCACCA CAGCCTCCAC TACCTCACCA CTCCGCCTGA 480
GCAAAAAAAA AAAAAAGGGT GGGCAGCATC CTGTGCCTGC TTCTCTTACC CACATCAACT 540
GCTGAGCCAG CTCGCCCCCA CAGCCTGCTT GCCTAGCTTG CTACCATGCC TGCTGTTGTT 600
CCTCACGTCA CAAGGCTGAA TGAAGCCTGG GGGGTGGGTG AAGTAGGTCT TTCAGTTGCG 660
AGCAGGACAG AGACCAGAGT GGCTGCTCTA AGGGCAGCCA TGCTTACCTA CTTGTTCATG 720
TCTCCCAGCA GAGCTGAACA CGGCAGCAGT CCTCCCACCA GGCCAGGAGG GGGTCTCTTC 780
CTACGTACGT AGTGTCAGAA GAGCCTGTGC ATGGCCTGTC ACACACAAGC TAGGATGTTC 840
CCTCCGCCAC TGTTGCAGAG TCCCATGAGC AATGTGAAAA TGTGGCAGGC CCAAGGTTTT 900
CTTCTCTGGT CCAGAGAGGG CGAGGCAAGA GCAGGAAGCA GGTTCTACAG CTCTGAGAAT 960
GCTGAGCTAG AGCAGCAGCC TCCAGGCAAA TGGGTTACCA AAGCAATTGC CTTCTGCCAG 1020
ACTGGGTGCT GGGGCCTCAG AGAGACTCCA GTATTCTTGC CTTCCTGAAA CCAGGGTCTA 1080
GCAGGACAAA ACATATTCCA ACTAGAGGTT GTCAATCTGG TGAAGGGTTG AGTAAACAGT 1140
AGAGGATGCA AGGCAGCCTG AGGTAAGTGC CAGACAGTCT CCGAAGATTC AGGCTGGCTC 1200
AGGCTTGCCT TGCCCCGTCA GTCATTGCTG GCTCTATGGC TATTACAGCC TGGGGTTGAA 1260
GGCTGGTTCT AGGGGTTCCT CCCACCAGCC CATAAATCTT AGTTACCAAG GGGCAGTCAG 1320
AGGCAGTCCC AGGGAGCCCA GCAATCCGTC TACACAGCAT TACAGCAAGC TGCAGTGTGA 1380
GCCAGAACTA ACAGGAGACA ACCCAAGCCT CCCTCCAGCT CTGGGAACCA GGCAAACCAT 1440
|
