Variant report

Variant	rs1873184
Chromosome Location	chr8:127833978-127833979
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 33 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:32)

rs_ID	r²[population]
rs10106550	0.85[AMR][1000 genomes]
rs10216500	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10216660	0.93[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10216757	0.92[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10216925	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10216939	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10505487	0.85[AMR][1000 genomes]
rs10505488	0.85[AMR][1000 genomes]
rs10505489	0.85[AMR][1000 genomes]
rs11987858	0.81[AMR][1000 genomes]
rs11989801	0.81[AMR][1000 genomes]
rs12547157	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs16901734	0.92[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs16901776	0.85[AMR][1000 genomes]
rs16901778	0.92[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs16901783	0.85[AMR][1000 genomes]
rs16901785	0.85[AMR][1000 genomes]
rs1873185	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28409662	0.85[AMR][1000 genomes]
rs28617317	0.85[AMR][1000 genomes]
rs6983290	0.93[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6984670	0.81[AMR][1000 genomes]
rs6993972	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6998093	0.85[AMR][1000 genomes]
rs7005373	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7012160	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7016582	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7016606	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs72722244	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs72722245	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7813029	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7816751	0.81[AMR][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	nsv891438	chr8:127670339-127845702	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:25 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:127827000-127837200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr8:127832000-127836600	Enhancers	Osteobl	bone
3	chr8:127832600-127834400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr8:127832600-127836600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
5	chr8:127832600-127836600	Weak transcription	Fetal Lung	lung
6	chr8:127832800-127834000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
7	chr8:127833000-127836200	Weak transcription	NHDF-Ad	bronchial
8	chr8:127833200-127837000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
9	chr8:127833400-127834200	Enhancers	Fetal Heart	heart
10	chr8:127833400-127834400	Enhancers	NH-A	brain
11	chr8:127833400-127836400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
12	chr8:127833400-127836400	Weak transcription	Fetal Muscle Leg	muscle
13	chr8:127833600-127834000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
14	chr8:127833600-127834400	Enhancers	Muscle Satellite Cultured Cells	--
15	chr8:127833600-127836200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
16	chr8:127833600-127836400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
17	chr8:127833600-127836800	Weak transcription	H1 Cell Line	embryonic stem cell
18	chr8:127833600-127839800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
19	chr8:127833800-127834000	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
20	chr8:127833800-127834000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
21	chr8:127833800-127834200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
22	chr8:127833800-127834400	Enhancers	NHEK	skin
23	chr8:127833800-127836600	Weak transcription	HUES6 Cell Line	embryonic stem cell
24	chr8:127833800-127837000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
25	chr8:127833800-127837000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell

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