Variant report

Variant	rs8095101
Chromosome Location	chr18:8107220-8107221
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 23 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:22)

rs_ID	r²[population]
rs16952894	1.00[CEU][hapmap];1.00[JPT][hapmap];0.81[AMR][1000 genomes];0.91[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs16952902	1.00[CEU][hapmap];0.90[CHB][hapmap];1.00[JPT][hapmap];0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs17397183	1.00[CEU][hapmap];1.00[JPT][hapmap];0.91[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs17397841	1.00[CEU][hapmap];0.80[CHB][hapmap];0.92[CHD][hapmap];0.83[GIH][hapmap];1.00[JPT][hapmap];0.88[TSI][hapmap];0.91[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs17475401	1.00[CEU][hapmap];1.00[JPT][hapmap];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1942956	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.88[GIH][hapmap];1.00[JPT][hapmap];1.00[TSI][hapmap];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4456614	1.00[CEU][hapmap];1.00[JPT][hapmap];0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs534675	0.89[ASN][1000 genomes]
rs538985	1.00[CEU][hapmap];0.92[CHD][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.88[TSI][hapmap];0.91[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs550672	1.00[CEU][hapmap];0.80[CHB][hapmap];0.92[CHD][hapmap];0.83[GIH][hapmap];1.00[JPT][hapmap];0.87[TSI][hapmap];0.91[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs557952	0.80[CHB][hapmap]
rs591062	0.80[CHB][hapmap]
rs641156	0.91[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs6506549	1.00[CEU][hapmap];0.89[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs687245	0.80[CHB][hapmap]
rs7236194	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7241382	0.91[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs73387768	1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs8082936	1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs8083862	1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs8099028	0.85[CEU][hapmap];1.00[JPT][hapmap];0.87[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs8099174	0.89[CEU][hapmap];1.00[CHD][hapmap];0.88[GIH][hapmap];1.00[JPT][hapmap];0.82[TSI][hapmap];0.87[EUR][1000 genomes];0.86[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv534374	chr18:7438812-8412546	Enhancers Strong transcription Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:30 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:8067400-8110200	Weak transcription	Right Ventricle	heart
2	chr18:8068600-8124800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr18:8084600-8108000	Weak transcription	Cortex derived primary cultured neurospheres	brain
4	chr18:8088800-8113400	Weak transcription	A549	lung
5	chr18:8092800-8122200	Weak transcription	Thymus	Thymus
6	chr18:8096600-8125000	Weak transcription	Pancreas	Pancrea
7	chr18:8102800-8126600	Weak transcription	Psoas Muscle	Psoas
8	chr18:8103000-8110400	Weak transcription	Left Ventricle	heart
9	chr18:8103400-8108600	Weak transcription	Fetal Kidney	kidney
10	chr18:8103400-8116400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
11	chr18:8103400-8116600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
12	chr18:8103400-8123800	Weak transcription	Duodenum Smooth Muscle	Duodenum
13	chr18:8103600-8110000	Weak transcription	Adipose Nuclei	Adipose
14	chr18:8103600-8110000	Weak transcription	Fetal Heart	heart
15	chr18:8103600-8116000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr18:8103600-8116400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
17	chr18:8103600-8117800	Weak transcription	Stomach Smooth Muscle	stomach
18	chr18:8103600-8122200	Weak transcription	Aorta	Aorta
19	chr18:8103600-8124800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
20	chr18:8103600-8136600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
21	chr18:8103600-8139200	Weak transcription	Brain Anterior Caudate	brain
22	chr18:8103800-8116200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr18:8104200-8132600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr18:8105600-8107600	Enhancers	Breast Myoepithelial Primary Cells	Breast
25	chr18:8105800-8107600	Enhancers	NHEK	skin
26	chr18:8106000-8107800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
27	chr18:8106800-8108000	Enhancers	HMEC	breast
28	chr18:8107200-8108000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
29	chr18:8107200-8108000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
30	chr18:8107200-8108200	Enhancers	HSMM	muscle

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