Variant report

Variant	rs73257221
Chromosome Location	chr6:166970410-166970411
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:166969437..166971704-chr6:167039008..167042376,3	MCF-7	breast:

Variant related genes	Relation type
ENSG00000071242	Chromatin interaction

Extended variants
information (count: 25 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:21)

rs_ID	r²[population]
rs11963778	0.89[AMR][1000 genomes]
rs11964118	1.00[AMR][1000 genomes]
rs11969154	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11969174	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11969176	1.00[AMR][1000 genomes]
rs11970618	0.89[AMR][1000 genomes]
rs16899123	0.89[AMR][1000 genomes]
rs16899126	1.00[AMR][1000 genomes]
rs16899129	1.00[AMR][1000 genomes]
rs16899150	1.00[AMR][1000 genomes]
rs16899151	1.00[AMR][1000 genomes]
rs16899157	1.00[AMR][1000 genomes]
rs57647994	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59061765	0.89[AMR][1000 genomes]
rs60005152	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs61045375	1.00[AMR][1000 genomes]
rs73255201	1.00[AMR][1000 genomes]
rs73257211	1.00[AMR][1000 genomes]
rs73257223	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73257240	1.00[AMR][1000 genomes]
rs73257242	0.89[AMR][1000 genomes]

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	esv3490076	chr6:166727901-167306743	Strong transcription Weak transcription Flanking Active TSS Genic enhancers Enhancers Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	25 gene(s)	inside rSNPs	diseases
2	esv3490077	chr6:166727901-167306743	Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	25 gene(s)	inside rSNPs	diseases
3	nsv886941	chr6:166907173-166996991	Strong transcription Weak transcription Genic enhancers Enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region miRNA	5 gene(s)	inside rSNPs	diseases
4	nsv5592	chr6:166958317-167002951	Weak transcription Flanking Active TSS Active TSS Enhancers ZNF genes & repeats Strong transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:84 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:166955200-166970600	Weak transcription	Pancreas	Pancrea
2	chr6:166955200-166970600	Weak transcription	Sigmoid Colon	Sigmoid Colon
3	chr6:166960000-166972800	Weak transcription	Primary neutrophils fromperipheralblood	blood
4	chr6:166964800-166972000	Enhancers	Cortex derived primary cultured neurospheres	brain
5	chr6:166965600-166971000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
6	chr6:166965800-166972400	Enhancers	Fetal Muscle Leg	muscle
7	chr6:166966000-166973600	Weak transcription	H9 Cell Line	embryonic stem cell
8	chr6:166966000-166974200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
9	chr6:166966200-166971200	Enhancers	Left Ventricle	heart
10	chr6:166966200-166978000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr6:166966400-166970800	Weak transcription	HUES64 Cell Line	embryonic stem cell
12	chr6:166966600-166970800	Weak transcription	HUES48 Cell Line	embryonic stem cell
13	chr6:166967000-166971200	Enhancers	Brain Angular Gyrus	brain
14	chr6:166967600-166970600	Enhancers	HUVEC	blood vessel
15	chr6:166967600-166971000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr6:166967600-166971000	Enhancers	Adipose Nuclei	Adipose
17	chr6:166967600-166971000	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
18	chr6:166967600-166971800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
19	chr6:166968000-166972000	Enhancers	Spleen	Spleen
20	chr6:166968000-166972800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr6:166968200-166972400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr6:166968400-166985800	Weak transcription	Fetal Kidney	kidney
23	chr6:166968800-166970600	Weak transcription	Ovary	ovary
24	chr6:166968800-166970800	Enhancers	HSMMtube	muscle
25	chr6:166968800-166971000	Enhancers	Breast Myoepithelial Primary Cells	Breast
26	chr6:166968800-166971600	Weak transcription	NHLF	lung
27	chr6:166968800-166973800	Enhancers	HMEC	breast
28	chr6:166969000-166970800	Enhancers	Gastric	stomach
29	chr6:166969000-166971000	Enhancers	Psoas Muscle	Psoas
30	chr6:166969000-166971000	Enhancers	Right Atrium	heart
31	chr6:166969000-166972400	Enhancers	Fetal Muscle Trunk	muscle
32	chr6:166969000-166973800	Genic enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
33	chr6:166969000-166974000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
34	chr6:166969200-166970600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
35	chr6:166969200-166970600	Weak transcription	Fetal Brain Male	brain
36	chr6:166969200-166972200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
37	chr6:166969200-166972200	Enhancers	Esophagus	oesophagus
38	chr6:166969400-166970600	Enhancers	Brain Substantia Nigra	brain
39	chr6:166969400-166970600	Weak transcription	Fetal Heart	heart
40	chr6:166969400-166978800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr6:166969600-166970600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr6:166969600-166970600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
43	chr6:166969600-166970600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
44	chr6:166969600-166970600	Enhancers	Stomach Mucosa	stomach
45	chr6:166969600-166970600	Enhancers	NHEK	skin
46	chr6:166969600-166971800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
47	chr6:166969800-166970600	Weak transcription	Lung	lung
48	chr6:166969800-166970600	Enhancers	Rectal Smooth Muscle	rectum
49	chr6:166969800-166971600	Weak transcription	Fetal Stomach	stomach
50	chr6:166969800-166971800	Enhancers	NH-A	brain

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