Variant report

Variant	rs2168218
Chromosome Location	chr15:33409861-33409862
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 21 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs12911944	0.82[JPT][hapmap]
rs12916976	0.82[ASN][1000 genomes]
rs17816808	0.82[ASN][1000 genomes]
rs2045188	0.94[CEU][hapmap];0.82[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs2045189	0.94[CEU][hapmap]
rs2444955	0.89[EUR][1000 genomes]
rs2468736	1.00[CEU][hapmap];0.94[EUR][1000 genomes]
rs2468737	0.96[EUR][1000 genomes]
rs2468761	0.83[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs345761	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs345763	0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs3861198	0.82[JPT][hapmap]
rs3861199	0.82[JPT][hapmap]
rs815481	0.89[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv903979	chr15:33144202-33550256	Active TSS Enhancers Weak transcription Strong transcription Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
2	nsv1052966	chr15:33149753-33541951	Weak transcription Flanking Active TSS Enhancers Strong transcription Active TSS Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
3	nsv542340	chr15:33149753-33541951	Flanking Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Active TSS Genic enhancers Bivalent Enhancer Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
4	nsv903981	chr15:33207082-33550256	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Strong transcription Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
5	nsv568918	chr15:33244672-33446971	Enhancers Flanking Active TSS ZNF genes & repeats Weak transcription Genic enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
6	nsv903982	chr15:33282844-33616150	Enhancers Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
7	nsv903983	chr15:33388030-33550256	Enhancers Active TSS Bivalent Enhancer Weak transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:18 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:33403600-33411400	Weak transcription	HSMM	muscle
2	chr15:33403800-33411400	Weak transcription	HSMMtube	muscle
3	chr15:33406400-33410200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
4	chr15:33406400-33411400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr15:33406400-33411400	Weak transcription	Pancreas	Pancrea
6	chr15:33406400-33418200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
7	chr15:33406800-33418400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr15:33407000-33418400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
9	chr15:33407800-33411400	Weak transcription	Fetal Lung	lung
10	chr15:33408000-33411400	Weak transcription	Placenta	Placenta
11	chr15:33408000-33411400	Weak transcription	Fetal Thymus	thymus
12	chr15:33408000-33412400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
13	chr15:33408000-33415800	Weak transcription	NHLF	lung
14	chr15:33408000-33416200	Weak transcription	Fetal Muscle Leg	muscle
15	chr15:33408200-33411400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
16	chr15:33408800-33412000	Weak transcription	Muscle Satellite Cultured Cells	--
17	chr15:33409400-33411800	Active TSS	Fetal Kidney	kidney
18	chr15:33409600-33410000	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin

Quick Search:

Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

what's new

Quick links