Variant report

Variant	rs9295147
Chromosome Location	chr6:161727937-161727938
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 67 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:44)

rs_ID	r²[population]
rs1079951	0.87[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs10945728	0.81[AMR][1000 genomes]
rs1111040	0.82[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12191683	0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12664801	0.82[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs13191963	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs13206420	0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs34129074	0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs35318741	0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6908327	0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6918112	0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6918267	0.83[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs6918480	0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6919764	0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6925844	0.92[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs6929474	0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6933275	0.95[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs6933430	0.89[EUR][1000 genomes]
rs6933448	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6939708	0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6940606	0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9295146	0.83[ASN][1000 genomes]
rs9347491	0.80[ASN][1000 genomes]
rs9347492	0.81[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs9347493	0.97[ASN][1000 genomes]
rs9347494	0.86[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9347496	0.91[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs9355885	0.97[ASN][1000 genomes]
rs9355886	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9355889	0.81[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9365271	0.97[ASN][1000 genomes]
rs9365273	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9365278	0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9365280	0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9456649	0.97[ASN][1000 genomes]
rs9456650	0.89[AMR][1000 genomes];0.84[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9456652	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9458187	0.97[ASN][1000 genomes]
rs9458189	0.97[ASN][1000 genomes]
rs9458190	0.97[ASN][1000 genomes]
rs9458192	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9458194	0.97[ASN][1000 genomes]
rs9458210	0.91[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs9458213	0.80[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:23 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv886817	chr6:161371621-161846654	Strong transcription Enhancers Weak transcription Genic enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
2	esv3381361	chr6:161373617-161864101	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
3	nsv949397	chr6:161592100-161812932	Weak transcription Strong transcription Flanking Active TSS Genic enhancers Enhancers ZNF genes & repeats Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
4	esv2752091	chr6:161592100-161855785	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
5	nsv1029727	chr6:161607680-161814295	Weak transcription Strong transcription Active TSS Enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
6	nsv1030623	chr6:161611170-161796985	Enhancers Weak transcription Genic enhancers Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
7	nsv538494	chr6:161611170-161796985	Flanking Active TSS Weak transcription Enhancers Strong transcription Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
8	nsv481931	chr6:161647026-161961906	Weak transcription Enhancers Genic enhancers Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
9	nsv533149	chr6:161653240-161769727	Active TSS Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
10	nsv1031234	chr6:161676768-162250726	Enhancers ZNF genes & repeats Weak transcription Active TSS Bivalent Enhancer Strong transcription Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
11	nsv869611	chr6:161690974-161817564	Enhancers Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
12	nsv1025168	chr6:161702621-161831885	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
13	nsv886819	chr6:161712035-162520133	Enhancers Flanking Active TSS Active TSS Weak transcription Bivalent Enhancer ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
14	nsv886820	chr6:161712880-162184932	Flanking Active TSS Enhancers ZNF genes & repeats Weak transcription Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
15	esv3474361	chr6:161726018-161728095	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
16	esv3474359	chr6:161726154-161728000	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
17	nsv820100	chr6:161726158-161728227	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
18	esv11242	chr6:161726247-161728479	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
19	nsv823910	chr6:161726247-161728794	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
20	nsv605049	chr6:161726980-161727945	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
21	esv13692	chr6:161727258-161728794	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
22	nsv605060	chr6:161727894-161728530	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
23	nsv605061	chr6:161727894-161728711	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:161722600-161735800	Weak transcription	Right Atrium	heart
2	chr6:161725600-161730200	Weak transcription	HMEC	breast
3	chr6:161726800-161729000	Enhancers	Brain Hippocampus Middle	brain
4	chr6:161727000-161728400	Enhancers	Brain Cingulate Gyrus	brain
5	chr6:161727400-161728600	Weak transcription	Brain Substantia Nigra	brain
6	chr6:161727600-161728000	Enhancers	K562	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links