Variant report

Variant	rs61777684
Chromosome Location	chr1:62553709-62553710
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 25 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs10127438	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs11207901	0.89[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs1964872	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs2025290	0.84[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs4255414	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs4915796	0.90[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs4915797	0.90[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs56777178	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs58323203	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs58585691	0.86[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs59295242	0.86[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs61777670	0.85[EUR][1000 genomes]
rs61777691	0.85[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs6684468	0.85[EUR][1000 genomes]
rs6688017	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs6700644	0.85[EUR][1000 genomes]
rs7512777	0.90[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs7531424	0.80[EUR][1000 genomes]
rs7535670	0.88[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs7537716	0.85[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1004446	chr1:62394631-62813533	Enhancers ZNF genes & repeats Weak transcription Bivalent/Poised TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	12 gene(s)	inside rSNPs	diseases
2	nsv534984	chr1:62394631-62813533	Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Strong transcription ZNF genes & repeats Bivalent/Poised TSS Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	12 gene(s)	inside rSNPs	diseases
3	nsv1001667	chr1:62407786-62649838	Weak transcription Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	5 gene(s)	inside rSNPs	diseases
4	nsv461650	chr1:62542717-62657530	Weak transcription Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	5 gene(s)	inside rSNPs	diseases
5	nsv546417	chr1:62542717-62657530	Enhancers Weak transcription ZNF genes & repeats Strong transcription Bivalent Enhancer Active TSS Flanking Active TSS Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:60 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:62484400-62562200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
2	chr1:62508200-62628400	Weak transcription	Colonic Mucosa	Colon
3	chr1:62532600-62557400	Weak transcription	Spleen	Spleen
4	chr1:62532600-62568200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr1:62532600-62569200	Weak transcription	H1 Cell Line	embryonic stem cell
6	chr1:62532600-62587600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr1:62532800-62569000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
8	chr1:62534400-62555000	Weak transcription	Ovary	ovary
9	chr1:62534400-62555400	Weak transcription	Left Ventricle	heart
10	chr1:62536000-62554400	Weak transcription	Skeletal Muscle Male	skeletal muscle
11	chr1:62536200-62619400	Weak transcription	Rectal Smooth Muscle	rectum
12	chr1:62536800-62557400	Weak transcription	Pancreatic Islets	Pancreatic Islet
13	chr1:62536800-62566000	Weak transcription	Gastric	stomach
14	chr1:62541600-62563000	Weak transcription	Lung	lung
15	chr1:62542400-62586800	Weak transcription	NHEK	skin
16	chr1:62542400-62587400	Weak transcription	HMEC	breast
17	chr1:62542600-62555400	Weak transcription	Fetal Heart	heart
18	chr1:62542600-62563000	Weak transcription	Aorta	Aorta
19	chr1:62543400-62569400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
20	chr1:62544000-62575800	Weak transcription	Skeletal Muscle Female	skeletal muscle
21	chr1:62544400-62555600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
22	chr1:62544800-62553800	Weak transcription	HepG2	liver
23	chr1:62545000-62574800	Weak transcription	Fetal Kidney	kidney
24	chr1:62545400-62555600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
25	chr1:62545400-62606800	Weak transcription	Placenta Amnion	Placenta Amnion
26	chr1:62545600-62554000	Weak transcription	Liver	Liver
27	chr1:62547000-62554000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
28	chr1:62548200-62594000	Weak transcription	Stomach Smooth Muscle	stomach
29	chr1:62548400-62629800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
30	chr1:62549800-62555600	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
31	chr1:62550000-62555600	Strong transcription	Fetal Intestine Large	intestine
32	chr1:62550000-62557000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
33	chr1:62550200-62554400	Strong transcription	Primary T helper cells fromperipheralblood	blood
34	chr1:62550200-62554400	Strong transcription	Duodenum Mucosa	Duodenum
35	chr1:62550200-62607800	Weak transcription	Right Ventricle	heart
36	chr1:62550400-62554400	Weak transcription	Duodenum Smooth Muscle	Duodenum
37	chr1:62550400-62555000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chr1:62550600-62558600	Weak transcription	Rectal Mucosa Donor 31	rectum
39	chr1:62551000-62555400	Weak transcription	Right Atrium	heart
40	chr1:62551400-62576000	Weak transcription	H9 Cell Line	embryonic stem cell
41	chr1:62551600-62554800	Weak transcription	HUES6 Cell Line	embryonic stem cell
42	chr1:62551800-62594200	Weak transcription	Primary T cells fromperipheralblood	blood
43	chr1:62551800-62614000	Weak transcription	Primary T cells from cord blood	blood
44	chr1:62552000-62554200	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
45	chr1:62552000-62555000	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
46	chr1:62552000-62555400	Weak transcription	HUES48 Cell Line	embryonic stem cell
47	chr1:62552000-62556000	Weak transcription	HUES64 Cell Line	embryonic stem cell
48	chr1:62552400-62555000	Strong transcription	Sigmoid Colon	Sigmoid Colon
49	chr1:62552400-62555200	Strong transcription	Esophagus	oesophagus
50	chr1:62552400-62555400	Weak transcription	iPS-15b Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links