Variant report

Variant	rs17029698
Chromosome Location	chr4:100919138-100919139
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr4:100918838..100919810-chr4:101016858..101017790,8	MCF-7	breast:
2	chr4:100919042..100919985-chr4:100984315..100985120,2	MCF-7	breast:
3	chr4:100914108..100916821-chr4:100918808..100921223,2	K562	blood:
4	chr4:100913310..100915550-chr4:100916884..100919803,2	MCF-7	breast:

Extended variants
information (count: 44 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:44)

rs_ID	r²[population]
rs10001730	1.00[AFR][1000 genomes];0.93[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs10002820	0.89[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs10014424	1.00[CEU][hapmap];0.93[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.92[AMR][1000 genomes];0.93[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10016741	0.92[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.88[AFR][1000 genomes];0.88[ASN][1000 genomes]
rs10018937	0.89[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs10461176	1.00[CEU][hapmap];0.93[CHB][hapmap];1.00[JPT][hapmap];0.86[ASN][1000 genomes]
rs1365494	1.00[ASW][hapmap];0.93[CHB][hapmap];0.93[CHD][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];0.88[YRI][hapmap];1.00[AFR][1000 genomes];0.88[ASN][1000 genomes]
rs17029542	1.00[JPT][hapmap]
rs17029577	1.00[JPT][hapmap]
rs17029592	0.83[CHD][hapmap];1.00[JPT][hapmap];0.88[MEX][hapmap]
rs17029594	0.83[CHD][hapmap];1.00[JPT][hapmap];0.88[MEX][hapmap]
rs17029601	1.00[YRI][hapmap];0.89[AFR][1000 genomes]
rs17029606	1.00[ASW][hapmap];0.85[CHB][hapmap];0.93[CHD][hapmap];1.00[JPT][hapmap];0.88[MEX][hapmap];1.00[YRI][hapmap];0.84[AFR][1000 genomes];0.85[ASN][1000 genomes]
rs17029641	1.00[ASW][hapmap];1.00[CEU][hapmap];0.93[CHB][hapmap];0.97[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];0.91[MKK][hapmap];0.91[TSI][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes];0.92[AMR][1000 genomes];0.93[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs17029667	1.00[ASW][hapmap];0.93[CHB][hapmap];0.97[CHD][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs17029681	0.98[ASN][1000 genomes]
rs17029696	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];0.91[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17029717	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs2282587	0.89[AFR][1000 genomes];0.85[ASN][1000 genomes]
rs2298734	1.00[CEU][hapmap];0.93[CHB][hapmap];1.00[JPT][hapmap];0.89[ASN][1000 genomes]
rs28375729	0.93[CHB][hapmap];0.97[CHD][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.93[ASN][1000 genomes]
rs28445732	0.89[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs28497573	0.84[AFR][1000 genomes];0.89[ASN][1000 genomes]
rs28553972	1.00[AFR][1000 genomes];0.92[AMR][1000 genomes];0.93[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs28561548	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];0.91[MKK][hapmap];0.91[TSI][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs28566137	1.00[AFR][1000 genomes];0.92[AMR][1000 genomes];0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs28604943	0.91[ASN][1000 genomes]
rs28635099	1.00[AFR][1000 genomes];0.92[AMR][1000 genomes];0.89[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2866175	1.00[ASW][hapmap];0.93[CHB][hapmap];0.97[CHD][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.87[ASN][1000 genomes]
rs28705829	0.83[AFR][1000 genomes]
rs28709045	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28824275	1.00[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs28893880	1.00[ASW][hapmap];1.00[CEU][hapmap];0.93[CHB][hapmap];0.97[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];0.91[MKK][hapmap];0.91[TSI][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.92[AMR][1000 genomes];0.89[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs3737485	1.00[JPT][hapmap]
rs3775510	0.85[ASN][1000 genomes]
rs4463078	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs57238114	0.84[AFR][1000 genomes];0.85[ASN][1000 genomes]
rs57862852	0.84[AFR][1000 genomes];0.85[ASN][1000 genomes]
rs59439986	0.94[ASN][1000 genomes]
rs59768994	0.91[ASN][1000 genomes]
rs60203069	0.91[ASN][1000 genomes]
rs60994806	0.84[AFR][1000 genomes];0.85[ASN][1000 genomes]
rs61229555	0.98[ASN][1000 genomes]
rs62305048	1.00[AFR][1000 genomes];0.88[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:100918600-100919400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
2	chr4:100918600-100920200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
3	chr4:100918800-100919200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
4	chr4:100918800-100919400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr4:100918800-100919400	Enhancers	NHDF-Ad	bronchial
6	chr4:100918800-100920200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr4:100918800-100920200	Enhancers	Muscle Satellite Cultured Cells	--
8	chr4:100918800-100920200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr4:100918800-100920600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr4:100919000-100919600	Enhancers	iPS-20b Cell Line	embryonic stem cell
11	chr4:100919000-100919600	Enhancers	Cortex derived primary cultured neurospheres	brain
12	chr4:100919000-100919800	Enhancers	ES-I3 Cell Line	embryonic stem cell
13	chr4:100919000-100919800	Enhancers	HUES64 Cell Line	embryonic stem cell
14	chr4:100919000-100919800	Enhancers	Brain Cingulate Gyrus	brain
15	chr4:100919000-100919800	Enhancers	A549	lung
16	chr4:100919000-100920000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
17	chr4:100919000-100920200	Enhancers	Brain Inferior Temporal Lobe	brain
18	chr4:100919000-100920200	Enhancers	NHEK	skin

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