Variant report

Variant	rs7743011
Chromosome Location	chr6:56375010-56375011
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:56371302..56373415-chr6:56374644..56377108,2	K562	blood:
2	chr6:56374485..56377341-chr6:56380470..56384676,4	MCF-7	breast:

Extended variants
information (count: 84 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:81)

rs_ID	r²[population]
rs11753813	1.00[CEU][hapmap];0.82[JPT][hapmap];0.82[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs11756977	0.91[CEU][hapmap];1.00[CHB][hapmap];0.94[JPT][hapmap];0.92[AMR][1000 genomes];0.90[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11759493	0.87[CEU][hapmap];0.82[JPT][hapmap]
rs12527139	0.87[EUR][1000 genomes]
rs13194746	0.95[AMR][1000 genomes];0.91[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs13219448	0.81[AMR][1000 genomes]
rs1535610	0.84[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs1535612	1.00[CEU][hapmap];0.82[JPT][hapmap];0.84[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs16887974	0.91[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2064591	0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2273973	1.00[CEU][hapmap];0.82[JPT][hapmap];0.82[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs2273974	0.83[CEU][hapmap];0.81[JPT][hapmap]
rs2397226	0.82[JPT][hapmap]
rs4130060	0.87[CEU][hapmap];0.82[JPT][hapmap];0.89[EUR][1000 genomes]
rs4143827	0.85[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4143828	0.87[CEU][hapmap];0.82[EUR][1000 genomes]
rs4236139	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[YRI][hapmap];0.94[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4236140	0.87[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[AMR][1000 genomes];0.89[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4236141	1.00[CEU][hapmap];0.82[JPT][hapmap];0.89[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs4236142	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs4236143	0.86[EUR][1000 genomes]
rs4236144	0.91[CEU][hapmap];0.82[EUR][1000 genomes]
rs4236145	0.87[CEU][hapmap];0.82[EUR][1000 genomes]
rs4283892	0.87[CEU][hapmap];0.82[JPT][hapmap]
rs4329120	0.83[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4346846	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.86[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4454141	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[YRI][hapmap];0.83[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4466244	0.82[AFR][1000 genomes];0.97[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs4472350	0.84[AFR][1000 genomes];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4473850	0.84[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4499917	0.87[CEU][hapmap];0.82[JPT][hapmap];0.83[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs4712132	0.87[CEU][hapmap];0.81[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs4712133	0.91[CEU][hapmap];0.92[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs4715625	0.83[CEU][hapmap];0.82[JPT][hapmap]
rs4715626	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4715627	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[YRI][hapmap];0.86[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4715628	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[YRI][hapmap];0.86[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4715629	1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[JPT][hapmap];0.82[YRI][hapmap];0.95[AMR][1000 genomes];0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4715630	0.87[CEU][hapmap];0.83[EUR][1000 genomes]
rs4715631	0.91[CEU][hapmap];1.00[CHB][hapmap];0.94[JPT][hapmap];0.92[AMR][1000 genomes];0.91[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6459161	0.91[CEU][hapmap]
rs6904202	1.00[CEU][hapmap];0.90[CHB][hapmap];0.88[JPT][hapmap];0.85[AMR][1000 genomes];0.89[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6906792	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[YRI][hapmap];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6907917	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs6914184	0.97[AMR][1000 genomes];0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6919608	0.86[CEU][hapmap];0.90[CHB][hapmap];0.93[JPT][hapmap];0.89[YRI][hapmap];0.81[AFR][1000 genomes];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6922770	1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[JPT][hapmap];0.84[YRI][hapmap];0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6939305	1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[AMR][1000 genomes];0.84[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs71549713	0.82[AMR][1000 genomes];0.81[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs721475	0.84[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs7741295	0.87[CEU][hapmap];0.82[JPT][hapmap];0.89[EUR][1000 genomes]
rs7749370	0.87[ASN][1000 genomes]
rs7755361	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[YRI][hapmap];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7755573	0.83[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs7758054	0.87[EUR][1000 genomes]
rs7759875	1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[JPT][hapmap];0.83[YRI][hapmap];0.95[AMR][1000 genomes];0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7760640	1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[JPT][hapmap];0.84[YRI][hapmap];0.95[AMR][1000 genomes];0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7760695	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs7761281	0.83[AMR][1000 genomes]
rs7762629	0.82[JPT][hapmap];0.84[EUR][1000 genomes]
rs9296848	0.87[CEU][hapmap];0.82[JPT][hapmap]
rs9296849	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9296850	0.87[CEU][hapmap];0.82[JPT][hapmap];0.83[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs9349826	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9357921	1.00[CEU][hapmap];0.82[JPT][hapmap];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9357922	0.82[JPT][hapmap];0.81[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs9367688	0.80[AMR][1000 genomes]
rs9370533	0.90[CEU][hapmap]
rs9370534	0.82[JPT][hapmap]
rs9370535	0.83[CEU][hapmap];0.82[JPT][hapmap]
rs9382635	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs9396213	0.86[CEU][hapmap]
rs9396214	0.82[CEU][hapmap];0.81[JPT][hapmap]
rs9396218	0.84[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs9396220	0.91[CEU][hapmap];1.00[CHB][hapmap];0.82[JPT][hapmap];0.89[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs9464389	0.89[EUR][1000 genomes]
rs9475709	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs9475711	0.85[ASN][1000 genomes]
rs9475713	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9475714	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[YRI][hapmap];0.87[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9475716	0.82[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv491933	chr6:56177722-57171010	Active TSS Enhancers Strong transcription Weak transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	51 gene(s)	inside rSNPs	diseases
2	nsv830666	chr6:56243743-56419599	Genic enhancers Weak transcription Strong transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS 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	9 gene(s)	inside rSNPs	diseases
3	nsv885912	chr6:56327849-56458836	Enhancers Weak transcription Strong transcription Active TSS Genic enhancers Flanking Active TSS 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 lncRNA	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:107 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:56337600-56376000	Weak transcription	Gastric	stomach
2	chr6:56341800-56407400	Weak transcription	Spleen	Spleen
3	chr6:56345000-56384200	Strong transcription	HUES64 Cell Line	embryonic stem cell
4	chr6:56351800-56386800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
5	chr6:56357000-56382600	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
6	chr6:56357000-56383600	Strong transcription	NH-A	brain
7	chr6:56357000-56384000	Strong transcription	HSMM	muscle
8	chr6:56357200-56384200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr6:56360400-56382200	Strong transcription	Osteobl	bone
10	chr6:56360600-56381800	Strong transcription	Muscle Satellite Cultured Cells	--
11	chr6:56360800-56377200	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr6:56362400-56391200	Weak transcription	Esophagus	oesophagus
13	chr6:56362600-56385800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
14	chr6:56362800-56400200	Weak transcription	Colonic Mucosa	Colon
15	chr6:56363000-56402200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
16	chr6:56364800-56378600	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
17	chr6:56365600-56379400	Weak transcription	Pancreatic Islets	Pancreatic Islet
18	chr6:56367000-56376600	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr6:56368400-56376800	Strong transcription	GM12878-XiMat	blood
20	chr6:56368400-56382400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr6:56368600-56375400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
22	chr6:56369400-56378800	Strong transcription	Fetal Muscle Trunk	muscle
23	chr6:56369400-56380600	Strong transcription	HSMMtube	muscle
24	chr6:56370000-56378000	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
25	chr6:56370000-56382600	Strong transcription	iPS-20b Cell Line	embryonic stem cell
26	chr6:56370600-56380400	Strong transcription	Cortex derived primary cultured neurospheres	brain
27	chr6:56371000-56375200	Strong transcription	Fetal Kidney	kidney
28	chr6:56371000-56378000	Enhancers	Fetal Heart	heart
29	chr6:56371200-56375200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
30	chr6:56371200-56380200	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
31	chr6:56371400-56376200	Weak transcription	Small Intestine	intestine
32	chr6:56371800-56375400	Strong transcription	Fetal Lung	lung
33	chr6:56372200-56378000	Genic enhancers	Liver	Liver
34	chr6:56372200-56384200	Weak transcription	Hela-S3	cervix
35	chr6:56372800-56376000	Weak transcription	Pancreas	Pancrea
36	chr6:56372800-56378600	Strong transcription	Adipose Nuclei	Adipose
37	chr6:56372800-56378800	Strong transcription	Fetal Muscle Leg	muscle
38	chr6:56372800-56380200	Weak transcription	Aorta	Aorta
39	chr6:56373000-56378200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
40	chr6:56373000-56378600	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
41	chr6:56373000-56382800	Strong transcription	HUES48 Cell Line	embryonic stem cell
42	chr6:56373000-56390800	Weak transcription	Placenta	Placenta
43	chr6:56373600-56378600	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
44	chr6:56373600-56379400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
45	chr6:56373800-56380200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
46	chr6:56374200-56376000	Weak transcription	Ovary	ovary
47	chr6:56374200-56383400	Weak transcription	Right Ventricle	heart
48	chr6:56374200-56387000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
49	chr6:56374200-56390800	Weak transcription	Lung	lung
50	chr6:56374200-56391000	Weak transcription	Right Atrium	heart

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links