Variant report

Variant	rs1975755
Chromosome Location	chr1:85882905-85882906
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 42 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:39)

rs_ID	r²[population]
rs1006988	0.84[CEU][hapmap];0.82[JPT][hapmap];0.90[EUR][1000 genomes]
rs1006989	0.83[AFR][1000 genomes]
rs10489510	0.89[CEU][hapmap]
rs10747318	0.89[CEU][hapmap];0.83[YRI][hapmap];0.83[AFR][1000 genomes]
rs10782549	0.88[CEU][hapmap];0.86[AFR][1000 genomes]
rs10873701	0.89[CEU][hapmap];0.83[YRI][hapmap];0.83[AFR][1000 genomes]
rs10873702	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.90[YRI][hapmap];0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11161606	0.83[YRI][hapmap]
rs1146374	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12033483	0.82[CEU][hapmap]
rs12034249	0.89[CEU][hapmap]
rs1342323	0.88[CEU][hapmap]
rs1357635	0.89[CEU][hapmap];0.85[AFR][1000 genomes]
rs1357636	0.88[CEU][hapmap]
rs1523994	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1523995	0.89[CEU][hapmap];0.83[AFR][1000 genomes]
rs1554597	0.86[YRI][hapmap]
rs1608537	0.86[AFR][1000 genomes]
rs17384213	0.89[CEU][hapmap]
rs17388696	0.82[CEU][hapmap]
rs1965876	0.86[AFR][1000 genomes]
rs2016104	0.89[CEU][hapmap];0.91[YRI][hapmap];0.87[AFR][1000 genomes]
rs2124139	0.88[CEU][hapmap]
rs2177461	0.87[YRI][hapmap]
rs2300633	0.89[CEU][hapmap]
rs2840319	0.86[AFR][1000 genomes]
rs539714	1.00[CEU][hapmap];0.87[YRI][hapmap]
rs561422	0.84[AFR][1000 genomes];0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs570121	0.89[ASN][1000 genomes]
rs6420965	0.84[AFR][1000 genomes]
rs659070	0.82[CEU][hapmap]
rs6672870	0.88[CEU][hapmap];0.86[YRI][hapmap]
rs6697083	0.84[JPT][hapmap]
rs72724608	0.82[AFR][1000 genomes]
rs7515261	0.89[CEU][hapmap];0.83[YRI][hapmap];0.83[AFR][1000 genomes]
rs7539738	0.81[AFR][1000 genomes]
rs7546931	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7547571	0.86[AFR][1000 genomes]
rs990916	0.89[CEU][hapmap]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1006994	chr1:85454304-86327679	Active TSS Enhancers Weak transcription Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	72 gene(s)	inside rSNPs	diseases
2	nsv830470	chr1:85820775-86014080	Enhancers Weak transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
3	nsv1008877	chr1:85843238-85897570	Enhancers Weak transcription ZNF genes & repeats Active TSS Strong transcription Genic enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:34 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:85873600-85885000	Weak transcription	Fetal Intestine Large	intestine
2	chr1:85873800-85885400	Weak transcription	Fetal Stomach	stomach
3	chr1:85873800-85887600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr1:85874000-85903800	Weak transcription	NHLF	lung
5	chr1:85874200-85903600	Weak transcription	Muscle Satellite Cultured Cells	--
6	chr1:85874400-85903600	Weak transcription	HepG2	liver
7	chr1:85874400-85904200	Weak transcription	NH-A	brain
8	chr1:85875400-85885600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr1:85877200-85885600	Weak transcription	H1 Cell Line	embryonic stem cell
10	chr1:85877600-85885800	Weak transcription	HSMMtube	muscle
11	chr1:85878000-85883800	Weak transcription	HUES48 Cell Line	embryonic stem cell
12	chr1:85878400-85883000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
13	chr1:85879200-85885600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
14	chr1:85880400-85884400	Weak transcription	Brain Hippocampus Middle	brain
15	chr1:85880400-85884400	Weak transcription	NHDF-Ad	bronchial
16	chr1:85880400-85887600	Weak transcription	Osteobl	bone
17	chr1:85880600-85884600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
18	chr1:85882000-85883000	Strong transcription	Fetal Intestine Small	intestine
19	chr1:85882000-85883200	Strong transcription	HSMM	muscle
20	chr1:85882400-85883000	Enhancers	Psoas Muscle	Psoas
21	chr1:85882400-85883200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
22	chr1:85882400-85884000	Enhancers	HUVEC	blood vessel
23	chr1:85882400-85885000	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
24	chr1:85882600-85883200	Enhancers	HUES6 Cell Line	embryonic stem cell
25	chr1:85882600-85883200	Enhancers	iPS-18 Cell Line	embryonic stem cell
26	chr1:85882800-85883000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
27	chr1:85882800-85883000	Enhancers	Right Atrium	heart
28	chr1:85882800-85883200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
29	chr1:85882800-85883200	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
30	chr1:85882800-85883200	Enhancers	Aorta	Aorta
31	chr1:85882800-85883200	Enhancers	Ovary	ovary
32	chr1:85882800-85883200	Enhancers	Pancreas	Pancrea
33	chr1:85882800-85883200	Enhancers	Skeletal Muscle Male	skeletal muscle
34	chr1:85882800-85883200	Enhancers	Skeletal Muscle Female	skeletal muscle

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links