Variant report

Variant	rs9328328
Chromosome Location	chr6:5703138-5703139
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

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

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs1001568	1.00[CHB][hapmap];0.94[JPT][hapmap];0.91[YRI][hapmap];0.94[AFR][1000 genomes];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1005521	0.87[CHB][hapmap];0.88[JPT][hapmap];0.83[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs11752777	0.94[CHB][hapmap]
rs12210617	0.82[EUR][1000 genomes]
rs13213128	0.88[CHB][hapmap]
rs2142738	0.94[CHB][hapmap]
rs2326634	0.94[CHB][hapmap]
rs4140654	0.88[CHB][hapmap];0.81[AMR][1000 genomes];0.85[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs4959347	0.88[CHB][hapmap]
rs4960125	0.82[CHB][hapmap]
rs6918561	0.94[CHB][hapmap]
rs6918675	1.00[CHB][hapmap];0.81[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs6935719	0.86[AMR][1000 genomes];0.88[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs760675	0.94[CHB][hapmap];0.89[JPT][hapmap];0.86[AMR][1000 genomes];0.87[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7739358	0.94[CHB][hapmap];0.84[JPT][hapmap];0.83[AMR][1000 genomes];0.85[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7742697	0.83[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7746913	0.88[CHB][hapmap]
rs877010	0.82[CHB][hapmap]
rs878988	0.88[CHB][hapmap];0.83[AMR][1000 genomes];0.86[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs9378439	0.93[ASN][1000 genomes]
rs9378979	0.94[CHB][hapmap]
rs9378980	0.82[CHB][hapmap]
rs9378983	0.94[CHB][hapmap];0.89[JPT][hapmap];0.81[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs9405281	0.88[CHB][hapmap]
rs9405859	0.88[CHB][hapmap]
rs9502329	0.87[AMR][1000 genomes];0.88[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9504488	0.88[CHB][hapmap]

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	esv3473790	chr6:5692573-5707035	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Active TSS	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
2	esv3473791	chr6:5692573-5707035	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Active TSS	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
3	nsv823407	chr6:5692735-5706712	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS Strong transcription	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
4	nsv981100	chr6:5703106-5706653	Weak transcription Enhancers Flanking Active TSS Strong transcription	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:26 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:5672200-5705800	Weak transcription	Thymus	Thymus
2	chr6:5673800-5709800	Weak transcription	Stomach Smooth Muscle	stomach
3	chr6:5678000-5709400	Weak transcription	Pancreas	Pancrea
4	chr6:5684800-5706000	Weak transcription	Ovary	ovary
5	chr6:5695800-5709800	Weak transcription	Fetal Stomach	stomach
6	chr6:5696200-5707600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
7	chr6:5696200-5712400	Weak transcription	Sigmoid Colon	Sigmoid Colon
8	chr6:5696400-5705400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
9	chr6:5699200-5705600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr6:5699400-5708000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
11	chr6:5699400-5713200	Weak transcription	Esophagus	oesophagus
12	chr6:5699600-5704000	Weak transcription	Lung	lung
13	chr6:5699600-5704800	Weak transcription	Dnd41	blood
14	chr6:5699800-5715800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
15	chr6:5700000-5705600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
16	chr6:5700400-5708200	Weak transcription	Primary B cells from cord blood	blood
17	chr6:5700800-5704200	Weak transcription	Primary monocytes fromperipheralblood	blood
18	chr6:5701600-5705600	Weak transcription	Aorta	Aorta
19	chr6:5701600-5706600	Weak transcription	Fetal Muscle Trunk	muscle
20	chr6:5701800-5707200	Weak transcription	Spleen	Spleen
21	chr6:5701800-5708600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
22	chr6:5702000-5705800	Enhancers	Primary T cells from cord blood	blood
23	chr6:5702400-5709400	Weak transcription	Fetal Lung	lung
24	chr6:5702600-5704000	Weak transcription	Monocytes-CD14+_RO01746	blood
25	chr6:5703000-5703800	Enhancers	Fetal Heart	heart
26	chr6:5703000-5706600	Enhancers	Fetal Thymus	thymus

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links