Variant report

Variant	rs13204171
Chromosome Location	chr6:2416117-2416118
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:2414672..2416357-chr6:2438734..2440972,2	K562	blood:
2	chr6:2413985..2416473-chr6:2426217..2428226,2	K562	blood:

Extended variants
information (count: 69 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:60)

rs_ID	r²[population]
rs11965611	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs11968173	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs12524370	0.91[AMR][1000 genomes]
rs12529088	0.87[CEU][hapmap];0.85[CHB][hapmap];0.95[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs13191094	0.82[CEU][hapmap];0.82[EUR][1000 genomes]
rs13194198	0.92[ASN][1000 genomes]
rs13198172	0.90[AMR][1000 genomes];0.85[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs13200914	0.81[CEU][hapmap];0.85[CHB][hapmap];0.89[AMR][1000 genomes]
rs13214285	0.97[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs13220248	0.87[CEU][hapmap];0.93[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs17135028	0.92[ASN][1000 genomes]
rs17536894	0.83[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs17608626	0.87[CEU][hapmap];0.85[CHB][hapmap];0.95[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs17609498	0.82[EUR][1000 genomes]
rs2073004	0.96[ASN][1000 genomes]
rs28360628	0.95[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs34172338	0.95[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs34610626	0.83[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs34854900	0.93[AFR][1000 genomes];0.93[AMR][1000 genomes];0.87[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs34901328	0.83[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs34932214	0.90[AMR][1000 genomes]
rs35182831	0.82[EUR][1000 genomes]
rs35590232	0.91[AMR][1000 genomes]
rs35892674	0.83[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs35918040	0.97[AMR][1000 genomes];0.90[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs3734504	0.87[CEU][hapmap];0.85[CHB][hapmap];0.95[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs3734505	0.87[CEU][hapmap];0.82[CHB][hapmap];0.97[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs3734507	0.80[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs3823107	0.92[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs4596531	0.95[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs4959176	0.90[AMR][1000 genomes]
rs4959177	0.87[AMR][1000 genomes]
rs4959180	0.93[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs4959181	0.90[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs4959182	0.93[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs4959184	0.96[ASN][1000 genomes]
rs4959654	0.92[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs4959658	0.81[CEU][hapmap];0.85[CHB][hapmap];0.82[EUR][1000 genomes]
rs4959661	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs4959662	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs4959663	0.87[CEU][hapmap];0.85[CHB][hapmap];0.82[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs4959665	0.85[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs56343276	0.83[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs59493792	0.83[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs62391186	0.91[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs6902556	0.91[AMR][1000 genomes]
rs6908555	0.84[CEU][hapmap];0.85[CHB][hapmap];0.82[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs6911665	0.87[CEU][hapmap];0.80[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs71552124	0.82[EUR][1000 genomes]
rs7738954	0.93[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs7755646	0.83[AMR][1000 genomes]
rs7773388	0.95[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs9501836	0.87[CEU][hapmap];0.85[CHB][hapmap];0.82[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs9501838	0.85[CEU][hapmap];0.85[CHB][hapmap];0.82[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs9503185	0.87[CEU][hapmap];0.85[CHB][hapmap];0.82[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs9503186	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs9503187	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs9503188	0.80[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs9503189	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs9791368	0.95[AMR][1000 genomes];0.87[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv531295	chr6:1773436-2724986	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	71 gene(s)	inside rSNPs	diseases
2	nsv883388	chr6:2093432-2514911	Strong transcription Enhancers ZNF genes & repeats Weak transcription Transcr. at gene 5' and 3' Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	62 gene(s)	inside rSNPs	diseases
3	nsv883389	chr6:2093432-2776303	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	87 gene(s)	inside rSNPs	diseases
4	nsv1021573	chr6:2246721-2832408	Enhancers ZNF genes & repeats Strong transcription Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	80 gene(s)	inside rSNPs	diseases
5	nsv538102	chr6:2246721-2832408	Weak transcription Enhancers Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Strong transcription Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	80 gene(s)	inside rSNPs	diseases
6	nsv883390	chr6:2265344-2584919	Weak transcription Enhancers Strong transcription ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	30 gene(s)	inside rSNPs	diseases
7	nsv883391	chr6:2282747-2507448	Flanking Active TSS Weak transcription Enhancers Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
8	nsv1016878	chr6:2375784-2680476	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Active TSS Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
9	nsv498004	chr6:2380300-3313587	Weak transcription Active TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Enhancers Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	163 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:2399800-2449200	Weak transcription	Stomach Smooth Muscle	stomach
2	chr6:2401200-2417400	Weak transcription	Pancreas	Pancrea
3	chr6:2401200-2421000	Weak transcription	Fetal Intestine Large	intestine
4	chr6:2401400-2426200	Weak transcription	Aorta	Aorta
5	chr6:2402200-2417400	Weak transcription	Primary hematopoietic stem cells	blood
6	chr6:2402200-2449200	Weak transcription	Left Ventricle	heart
7	chr6:2405000-2417800	Weak transcription	Primary T cells from cord blood	blood
8	chr6:2414600-2434600	Weak transcription	Fetal Intestine Small	intestine
9	chr6:2414600-2452000	Weak transcription	Ovary	ovary
10	chr6:2414800-2448800	Weak transcription	Liver	Liver
11	chr6:2414800-2449200	Weak transcription	Fetal Stomach	stomach
12	chr6:2415800-2416400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr6:2416000-2427400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived

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