Variant report

Variant	rs35255677
Chromosome Location	chr2:98567820-98567821
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr2:98561365..98564019-chr2:98567762..98570732,2	K562	blood:
2	chr2:98541538..98543544-chr2:98565901..98567946,2	MCF-7	breast:

Extended variants
information (count: 83 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:73)

rs_ID	r²[population]
rs10432626	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs11678591	0.84[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs11679828	0.91[AFR][1000 genomes];0.84[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs11680018	0.85[EUR][1000 genomes]
rs11680321	0.81[EUR][1000 genomes]
rs11680883	0.86[EUR][1000 genomes]
rs11681535	0.85[EUR][1000 genomes]
rs11684749	0.81[EUR][1000 genomes]
rs11688829	0.94[AFR][1000 genomes];0.84[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs11690687	0.85[EUR][1000 genomes]
rs11690737	0.85[EUR][1000 genomes]
rs11691494	0.81[EUR][1000 genomes]
rs11692010	0.81[EUR][1000 genomes]
rs11692470	0.91[AFR][1000 genomes];0.84[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs12052222	0.84[EUR][1000 genomes]
rs12052836	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs12052846	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs12104810	0.84[EUR][1000 genomes]
rs12988571	0.81[EUR][1000 genomes]
rs12995673	0.81[EUR][1000 genomes]
rs13008968	0.83[EUR][1000 genomes]
rs13020776	0.81[EUR][1000 genomes]
rs13023980	0.84[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs13028954	0.84[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs13032265	0.81[EUR][1000 genomes]
rs13032883	0.91[AFR][1000 genomes];0.87[AMR][1000 genomes];0.94[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs13034929	0.81[EUR][1000 genomes]
rs1470483	0.81[EUR][1000 genomes]
rs17489454	0.81[EUR][1000 genomes]
rs17489915	0.81[EUR][1000 genomes]
rs17489984	0.81[EUR][1000 genomes]
rs17490429	0.83[AFR][1000 genomes];0.84[EUR][1000 genomes]
rs1838797	0.84[EUR][1000 genomes]
rs1875699	0.97[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs2044458	0.81[EUR][1000 genomes]
rs2044459	0.83[AFR][1000 genomes];0.84[EUR][1000 genomes]
rs2084176	0.83[AFR][1000 genomes];0.84[EUR][1000 genomes]
rs2278700	0.82[EUR][1000 genomes]
rs2305143	0.81[EUR][1000 genomes]
rs2871183	0.81[EUR][1000 genomes]
rs3198055	0.89[AFR][1000 genomes];0.86[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs34373359	0.83[AFR][1000 genomes];0.84[EUR][1000 genomes]
rs34502870	0.81[EUR][1000 genomes]
rs34503448	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs34528940	0.83[EUR][1000 genomes]
rs34654057	0.81[EUR][1000 genomes]
rs34974566	0.93[AFR][1000 genomes];0.84[AMR][1000 genomes];0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs35098301	0.97[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs35218942	0.90[AFR][1000 genomes];0.84[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs35424768	0.81[EUR][1000 genomes]
rs35505530	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs35564270	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs35783535	0.97[AFR][1000 genomes];0.87[AMR][1000 genomes];0.94[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4311104	0.81[EUR][1000 genomes]
rs55776387	0.81[EUR][1000 genomes]
rs55861914	0.84[AFR][1000 genomes]
rs55886305	0.81[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs57836517	0.80[AFR][1000 genomes]
rs58546246	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs62156511	0.84[AFR][1000 genomes];0.83[AMR][1000 genomes];0.89[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs6710088	0.83[AMR][1000 genomes]
rs6711101	0.81[EUR][1000 genomes]
rs6738389	0.81[EUR][1000 genomes]
rs6746768	0.85[EUR][1000 genomes]
rs6748124	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs6757357	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs71412824	0.81[EUR][1000 genomes]
rs717417	0.81[EUR][1000 genomes]
rs7421146	0.83[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs7564773	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs7583868	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs7601898	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs953320	0.89[AMR][1000 genomes];0.95[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv526360	chr2:98403683-98814054	Weak transcription Strong transcription Active TSS Enhancers Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	nsv521568	chr2:98403683-98826203	Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
3	nsv1004220	chr2:98423421-98816010	Weak transcription Enhancers Bivalent Enhancer Strong transcription Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
4	nsv1007259	chr2:98429744-98818080	Enhancers Weak transcription Active TSS Bivalent Enhancer Strong transcription Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
5	nsv535832	chr2:98429744-98818080	Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Strong transcription Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
6	nsv1009218	chr2:98442640-98816010	Strong transcription Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
7	nsv1003925	chr2:98442640-98821102	Enhancers Strong transcription Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
8	nsv999442	chr2:98448732-98816010	Weak transcription Enhancers Flanking Bivalent TSS/Enh Active TSS Genic enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
9	nsv1013902	chr2:98454309-98818080	ZNF genes & repeats Weak transcription Bivalent/Poised TSS Active TSS Enhancers Strong transcription Genic enhancers Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
10	nsv1013416	chr2:98472701-98688729	Enhancers Flanking Active TSS Weak transcription Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:82 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:98554000-98570200	Weak transcription	Primary B cells from cord blood	blood
2	chr2:98561800-98570200	Weak transcription	Primary T cells from cord blood	blood
3	chr2:98562200-98570400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
4	chr2:98562400-98569200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
5	chr2:98562600-98568000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
6	chr2:98562600-98570000	Weak transcription	Fetal Intestine Small	intestine
7	chr2:98562600-98570200	Weak transcription	Fetal Lung	lung
8	chr2:98563400-98570600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
9	chr2:98563600-98569600	Weak transcription	Rectal Mucosa Donor 31	rectum
10	chr2:98563600-98589200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
11	chr2:98564600-98580600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
12	chr2:98565400-98569200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
13	chr2:98565600-98568400	Enhancers	HMEC	breast
14	chr2:98565800-98568400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
15	chr2:98565800-98568400	Enhancers	NHLF	lung
16	chr2:98566000-98568200	Enhancers	Left Ventricle	heart
17	chr2:98566000-98569400	Enhancers	Placenta	Placenta
18	chr2:98566200-98568400	Enhancers	HSMM	muscle
19	chr2:98566200-98570600	Weak transcription	Primary monocytes fromperipheralblood	blood
20	chr2:98566400-98568000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
21	chr2:98566400-98568200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
22	chr2:98566400-98568200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
23	chr2:98566400-98568200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
24	chr2:98566400-98568200	Weak transcription	Aorta	Aorta
25	chr2:98566400-98568200	Enhancers	Placenta Amnion	Placenta Amnion
26	chr2:98566400-98568200	Enhancers	NH-A	brain
27	chr2:98566400-98568400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr2:98566400-98568400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
29	chr2:98566400-98568600	Enhancers	NHDF-Ad	bronchial
30	chr2:98566600-98568200	Enhancers	Adipose Nuclei	Adipose
31	chr2:98566600-98571000	Enhancers	Primary B cells from peripheral blood	blood
32	chr2:98566800-98568000	Enhancers	Brain Cingulate Gyrus	brain
33	chr2:98566800-98568000	Enhancers	Skeletal Muscle Male	skeletal muscle
34	chr2:98566800-98568200	Enhancers	Psoas Muscle	Psoas
35	chr2:98566800-98568200	Enhancers	Sigmoid Colon	Sigmoid Colon
36	chr2:98566800-98568200	Enhancers	A549	lung
37	chr2:98566800-98568200	Enhancers	HSMMtube	muscle
38	chr2:98566800-98568400	Enhancers	Primary T helper cells PMA-I stimulated	--
39	chr2:98566800-98568400	Enhancers	Skeletal Muscle Female	skeletal muscle
40	chr2:98566800-98569200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
41	chr2:98566800-98569200	Enhancers	Breast Myoepithelial Primary Cells	Breast
42	chr2:98567000-98568000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
43	chr2:98567000-98570400	Enhancers	GM12878-XiMat	blood
44	chr2:98567000-98574400	Weak transcription	Lung	lung
45	chr2:98567200-98568000	Enhancers	Duodenum Mucosa	Duodenum
46	chr2:98567200-98568200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
47	chr2:98567200-98568400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
48	chr2:98567200-98568400	Enhancers	Osteobl	bone
49	chr2:98567200-98569000	Weak transcription	Esophagus	oesophagus
50	chr2:98567200-98574200	Weak transcription	Small Intestine	intestine

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