Variant report

Variant	rs35321446
Chromosome Location	chr2:98356712-98356713
allele	C/G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr2:98326109..98328548-chr2:98356181..98358918,2	MCF-7	breast:
2	chr2:98355724..98358443-chr2:98358896..98360638,2	MCF-7	breast:

Extended variants
information (count: 31 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:29)

rs_ID	r²[population]
rs10460480	0.89[ASN][1000 genomes]
rs11687510	0.84[ASN][1000 genomes]
rs11691641	0.83[EUR][1000 genomes]
rs12053205	0.83[ASN][1000 genomes]
rs13002912	0.80[EUR][1000 genomes]
rs1562293	0.86[ASN][1000 genomes]
rs17033906	0.95[ASN][1000 genomes]
rs2084177	0.84[EUR][1000 genomes]
rs2121272	0.92[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs2278699	0.95[ASN][1000 genomes]
rs2289918	0.95[ASN][1000 genomes]
rs2289919	0.93[ASN][1000 genomes]
rs34747246	0.92[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs56293187	0.95[ASN][1000 genomes]
rs56948188	0.91[ASN][1000 genomes]
rs57831860	0.95[ASN][1000 genomes]
rs58019724	0.85[ASN][1000 genomes]
rs58511420	0.95[ASN][1000 genomes]
rs59562515	0.85[ASN][1000 genomes]
rs61228852	0.83[ASN][1000 genomes]
rs62157588	0.92[AMR][1000 genomes];0.81[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6543040	0.87[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs6711959	0.95[ASN][1000 genomes]
rs6724539	0.83[AMR][1000 genomes]
rs72951160	0.95[ASN][1000 genomes]
rs73963109	0.95[ASN][1000 genomes]
rs746003	0.95[ASN][1000 genomes]
rs746004	0.95[ASN][1000 genomes]
rs7565744	0.95[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv531382	chr2:98250628-98457616	Weak transcription Enhancers Active TSS Strong transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
2	nsv874696	chr2:98309882-98362907	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:38 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:98336400-98361400	Weak transcription	Primary B cells from cord blood	blood
2	chr2:98336600-98358800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
3	chr2:98337800-98357400	Strong transcription	Dnd41	blood
4	chr2:98338800-98358800	Strong transcription	Thymus	Thymus
5	chr2:98339600-98357200	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
6	chr2:98342600-98357200	Strong transcription	Primary T cells from cord blood	blood
7	chr2:98343600-98357200	Weak transcription	Rectal Mucosa Donor 29	rectum
8	chr2:98344800-98356800	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
9	chr2:98345000-98366400	Weak transcription	Duodenum Mucosa	Duodenum
10	chr2:98346000-98357000	Strong transcription	Primary T helper cells fromperipheralblood	blood
11	chr2:98347000-98360600	Weak transcription	Skeletal Muscle Female	skeletal muscle
12	chr2:98347200-98357400	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
13	chr2:98347200-98358800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
14	chr2:98348200-98372400	Weak transcription	Esophagus	oesophagus
15	chr2:98348800-98364600	Weak transcription	HUES6 Cell Line	embryonic stem cell
16	chr2:98349000-98356800	Strong transcription	Primary T helper cells PMA-I stimulated	--
17	chr2:98350000-98360400	Weak transcription	Fetal Intestine Small	intestine
18	chr2:98351000-98357000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
19	chr2:98351600-98357200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
20	chr2:98352200-98398800	Weak transcription	Pancreatic Islets	Pancreatic Islet
21	chr2:98353400-98358400	Genic enhancers	Primary Natural Killer cells fromperipheralblood	blood
22	chr2:98354200-98357200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
23	chr2:98354200-98357400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
24	chr2:98354400-98358800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
25	chr2:98354400-98368200	Weak transcription	Colonic Mucosa	Colon
26	chr2:98355000-98359600	Genic enhancers	Primary T cells fromperipheralblood	blood
27	chr2:98355000-98373200	Weak transcription	Gastric	stomach
28	chr2:98355600-98357000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
29	chr2:98356200-98356800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
30	chr2:98356200-98358000	Genic enhancers	Primary T helper 17 cells PMA-I stimulated	--
31	chr2:98356400-98357000	Strong transcription	Fetal Thymus	thymus
32	chr2:98356400-98357800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
33	chr2:98356600-98357000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
34	chr2:98356600-98357200	Enhancers	Primary T killer memory cells from peripheral blood	blood
35	chr2:98356600-98358200	Weak transcription	Spleen	Spleen
36	chr2:98356600-98360000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
37	chr2:98356600-98360200	Weak transcription	Cortex derived primary cultured neurospheres	brain
38	chr2:98356600-98362000	Weak transcription	Colon Smooth Muscle	Colon

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