Variant report

Variant	rs55852703
Chromosome Location	chr7:99315856-99315857
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 92 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:88)

rs_ID	r²[population]
rs10211	0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10229552	0.84[ASN][1000 genomes]
rs10242455	0.85[ASN][1000 genomes]
rs10258552	0.81[ASN][1000 genomes]
rs10282706	0.83[ASN][1000 genomes]
rs12334072	0.82[ASN][1000 genomes]
rs12334077	0.84[ASN][1000 genomes]
rs12360	0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs13362853	0.83[ASN][1000 genomes]
rs1357319	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1403196	0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs15524	0.85[ASN][1000 genomes]
rs1818797	0.92[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1851425	0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1851427	0.86[ASN][1000 genomes]
rs1859690	0.82[ASN][1000 genomes]
rs1879859	0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2005548	0.80[ASN][1000 genomes]
rs2037497	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2037498	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2037499	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2090949	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2140128	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2177180	0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2222411	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2257401	0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2404769	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2404770	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2687072	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2687075	0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2687076	0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2687077	0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2687078	0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2687079	0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2687081	0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2687084	0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2687085	0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2687086	0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2687087	0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2687133	0.98[ASN][1000 genomes]
rs2687134	0.98[ASN][1000 genomes]
rs2687135	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2687136	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2687137	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2687139	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2687140	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2687141	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2687142	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2687143	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2687144	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2687145	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2740558	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2740559	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2740560	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2740561	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2740562	0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2740563	0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2740565	0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2741872	0.98[ASN][1000 genomes]
rs2948343	0.97[ASN][1000 genomes]
rs2948344	0.97[ASN][1000 genomes]
rs3735453	0.83[ASN][1000 genomes]
rs45442295	0.88[ASN][1000 genomes]
rs45600842	0.88[ASN][1000 genomes]
rs45624139	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4646450	0.85[ASN][1000 genomes]
rs4646457	0.85[ASN][1000 genomes]
rs4646461	0.98[AFR][1000 genomes];0.85[AMR][1000 genomes];0.81[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4646462	0.86[ASN][1000 genomes]
rs4646465	0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs58649180	0.81[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs59172435	0.86[ASN][1000 genomes]
rs59836234	0.82[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs60298785	0.86[ASN][1000 genomes]
rs61593387	0.86[ASN][1000 genomes]
rs6465750	0.86[ASN][1000 genomes]
rs72494453	0.84[ASN][1000 genomes]
rs72494454	0.86[ASN][1000 genomes]
rs72494455	0.81[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs72494456	0.86[ASN][1000 genomes]
rs73410654	0.82[AFR][1000 genomes];0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs776739	0.81[EUR][1000 genomes]
rs776742	0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs776744	0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs776745	0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs776746	0.88[ASN][1000 genomes]
rs7808022	0.81[ASN][1000 genomes]
rs939955	0.86[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv482532	chr7:99205906-99363886	Flanking Active TSS Enhancers Strong transcription Weak transcription Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
2	nsv970911	chr7:99275492-99333590	Enhancers ZNF genes & repeats Flanking Active TSS Weak transcription Strong transcription Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv888771	chr7:99294762-99355278	Enhancers Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	3 gene(s)	inside rSNPs	diseases
4	esv3378448	chr7:99295540-99331065	Weak transcription Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:21 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:99297800-99316200	Weak transcription	Gastric	stomach
2	chr7:99297800-99317400	Weak transcription	Rectal Mucosa Donor 31	rectum
3	chr7:99303200-99318200	Weak transcription	Fetal Heart	heart
4	chr7:99303200-99337200	Weak transcription	Skeletal Muscle Female	skeletal muscle
5	chr7:99304800-99318000	Weak transcription	Primary T helper cells fromperipheralblood	blood
6	chr7:99305600-99317600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
7	chr7:99306000-99339000	Weak transcription	Stomach Smooth Muscle	stomach
8	chr7:99306200-99317800	Weak transcription	Adipose Nuclei	Adipose
9	chr7:99306800-99340800	Weak transcription	Brain Cingulate Gyrus	brain
10	chr7:99307200-99317200	Weak transcription	Primary T cells from cord blood	blood
11	chr7:99307200-99334400	Weak transcription	Left Ventricle	heart
12	chr7:99307400-99318000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
13	chr7:99308200-99317600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr7:99311800-99317600	Weak transcription	K562	blood
15	chr7:99311800-99318400	Weak transcription	Pancreas	Pancrea
16	chr7:99311800-99349000	Weak transcription	Duodenum Smooth Muscle	Duodenum
17	chr7:99312000-99317400	Weak transcription	Duodenum Mucosa	Duodenum
18	chr7:99314800-99334400	Weak transcription	Esophagus	oesophagus
19	chr7:99315600-99316800	Weak transcription	Liver	Liver
20	chr7:99315600-99318400	Weak transcription	Sigmoid Colon	Sigmoid Colon
21	chr7:99315600-99331200	Weak transcription	Aorta	Aorta

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