Variant report

Variant	rs2736277
Chromosome Location	chr8:11218893-11218894
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr8:11212238..11213947-chr8:11218852..11221758,2	MCF-7	breast:
2	chr8:11218476..11220050-chr8:11220905..11223351,2	K562	blood:

Variant related genes	Relation type
ENSG00000154316	Chromatin interaction

Extended variants
information (count: 84 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:73)

rs_ID	r²[population]
rs10096194	0.84[CEU][hapmap];0.84[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs10098322	0.81[CEU][hapmap];0.81[JPT][hapmap]
rs10098488	0.84[CEU][hapmap]
rs10110557	0.81[CEU][hapmap];0.84[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs10503421	0.84[CEU][hapmap];0.85[EUR][1000 genomes]
rs11250127	0.96[CEU][hapmap]
rs11250129	0.82[CHB][hapmap];0.86[CHD][hapmap];0.83[MEX][hapmap];0.80[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs11774673	0.82[EUR][1000 genomes]
rs11781375	0.82[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs11784458	0.82[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs11784544	0.82[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs11991153	0.80[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs11994376	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs1435273	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs17741537	0.84[CEU][hapmap];0.84[GIH][hapmap];0.93[JPT][hapmap];0.90[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs17797443	0.96[CEU][hapmap]
rs17797894	0.84[CEU][hapmap];0.80[JPT][hapmap];0.88[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs1897950	0.96[CEU][hapmap]
rs1962656	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs2060456	0.84[CEU][hapmap];0.84[GIH][hapmap];0.88[JPT][hapmap];0.92[MEX][hapmap];0.90[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs2060457	0.81[CEU][hapmap];0.84[GIH][hapmap];0.88[JPT][hapmap];0.92[MEX][hapmap];0.90[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs2060459	0.84[CEU][hapmap];0.84[GIH][hapmap];0.88[JPT][hapmap];0.91[MEX][hapmap];0.90[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs2060465	0.96[CEU][hapmap];0.84[GIH][hapmap]
rs2099456	0.88[CEU][hapmap]
rs2164272	0.96[CEU][hapmap];0.84[GIH][hapmap]
rs2164273	0.96[CEU][hapmap];0.84[GIH][hapmap]
rs2293855	0.92[CEU][hapmap];0.86[GIH][hapmap]
rs2293856	1.00[CEU][hapmap];0.86[GIH][hapmap]
rs2293858	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs2293859	0.81[CEU][hapmap];0.84[GIH][hapmap];0.93[JPT][hapmap];0.92[MEX][hapmap];0.90[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs2293860	0.84[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.87[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2572397	0.80[CEU][hapmap]
rs2572398	0.80[CEU][hapmap]
rs2572417	0.80[CEU][hapmap]
rs2572418	0.80[CEU][hapmap]
rs34237267	0.80[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs35687566	0.84[AMR][1000 genomes]
rs35747588	0.83[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs3779891	0.84[CEU][hapmap]
rs3808509	0.96[CEU][hapmap]
rs3808513	0.96[CEU][hapmap];0.84[GIH][hapmap]
rs3808518	0.88[CEU][hapmap];0.86[GIH][hapmap]
rs4394351	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs4413734	0.84[CEU][hapmap];0.84[GIH][hapmap];0.88[JPT][hapmap];0.92[MEX][hapmap];0.90[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs4568582	0.96[CEU][hapmap]
rs5029571	0.84[CEU][hapmap];0.84[GIH][hapmap];0.88[JPT][hapmap];0.92[MEX][hapmap];0.90[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs58283816	0.82[EUR][1000 genomes]
rs62488721	0.80[EUR][1000 genomes]
rs6601578	0.92[CEU][hapmap]
rs6601580	0.82[EUR][1000 genomes]
rs6985146	0.96[CEU][hapmap];0.84[GIH][hapmap]
rs6985460	0.96[CEU][hapmap];0.84[GIH][hapmap]
rs6988922	0.82[EUR][1000 genomes]
rs6991606	0.96[CEU][hapmap]
rs6995404	0.81[CEU][hapmap]
rs7005469	0.84[CEU][hapmap];0.81[JPT][hapmap];0.82[EUR][1000 genomes]
rs7008205	0.80[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs7016671	0.81[CEU][hapmap]
rs718427	0.84[CEU][hapmap]
rs7815463	0.88[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs7815802	0.82[EUR][1000 genomes]
rs7815804	0.80[EUR][1000 genomes]
rs7816601	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs7816636	0.82[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs7817658	0.83[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs7819395	0.81[CEU][hapmap];0.86[JPT][hapmap];0.88[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs7820895	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs7828711	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs7831346	0.82[EUR][1000 genomes]
rs7833966	0.83[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs7834139	0.83[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs7838897	0.81[CEU][hapmap];0.81[JPT][hapmap];0.84[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs7839053	0.81[CEU][hapmap];0.84[AMR][1000 genomes];0.85[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1035072	chr8:10819444-11480692	Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription Strong transcription Flanking Active TSS Bivalent/Poised TSS Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
2	nsv539473	chr8:10819444-11480692	Weak transcription Flanking Active TSS Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
3	nsv529399	chr8:10970091-11805960	Enhancers Strong transcription Weak transcription Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
4	nsv831233	chr8:11046854-11234384	Weak transcription Enhancers Bivalent/Poised TSS Flanking Active TSS Strong transcription Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
5	nsv1022525	chr8:11066191-11309356	Enhancers Genic enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
6	nsv539474	chr8:11066191-11309356	Flanking Active TSS Weak transcription Enhancers Bivalent Enhancer Active TSS Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
7	nsv1033312	chr8:11126800-11252170	Flanking Active TSS Weak transcription Strong transcription Bivalent/Poised TSS Bivalent Enhancer Enhancers Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
8	nsv890354	chr8:11176147-11266131	Bivalent Enhancer Strong transcription Weak transcription ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Enhancers Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
9	esv34097	chr8:11177372-11489894	Weak transcription Flanking Active TSS Enhancers Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
10	nsv890355	chr8:11202154-11219334	Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Active TSS ZNF genes & repeats Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
11	nsv890356	chr8:11202154-11223022	Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Weak transcription Bivalent Enhancer Strong transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs2736277	MTMR9	Cis_1M	lymphoblastoid	RTeQTL
rs2736277	C8orf5	Cis_1M	lymphoblastoid	RTeQTL

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:11206200-11225000	Weak transcription	Psoas Muscle	Psoas
2	chr8:11206400-11226400	Weak transcription	Brain Anterior Caudate	brain
3	chr8:11207200-11223600	Weak transcription	Brain Hippocampus Middle	brain
4	chr8:11208000-11222400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr8:11210000-11224000	Weak transcription	Brain Angular Gyrus	brain
6	chr8:11212400-11219400	Weak transcription	Skeletal Muscle Male	skeletal muscle
7	chr8:11212800-11223600	Weak transcription	HUES48 Cell Line	embryonic stem cell
8	chr8:11214600-11221000	Weak transcription	Skeletal Muscle Female	skeletal muscle
9	chr8:11216000-11227400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
10	chr8:11216800-11222200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr8:11218000-11224000	Weak transcription	H9 Cell Line	embryonic stem cell
12	chr8:11218000-11237600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr8:11218200-11220200	Enhancers	Stomach Mucosa	stomach
14	chr8:11218200-11220800	Weak transcription	K562	blood
15	chr8:11218200-11221400	Weak transcription	Gastric	stomach
16	chr8:11218400-11219000	Enhancers	A549	lung
17	chr8:11218400-11219600	Weak transcription	Pancreas	Pancrea
18	chr8:11218600-11219600	Flanking Active TSS	HepG2	liver
19	chr8:11218800-11219400	Flanking Active TSS	Duodenum Mucosa	Duodenum
20	chr8:11218800-11219800	Enhancers	Fetal Intestine Small	intestine
21	chr8:11218800-11220200	Enhancers	Fetal Intestine Large	intestine

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links