Variant report

Variant	rs73257223
Chromosome Location	chr6:166970877-166970878
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]
rs73257221	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:78 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:166960000-166972800	Weak transcription	Primary neutrophils fromperipheralblood	blood
2	chr6:166964800-166972000	Enhancers	Cortex derived primary cultured neurospheres	brain
3	chr6:166965600-166971000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
4	chr6:166965800-166972400	Enhancers	Fetal Muscle Leg	muscle
5	chr6:166966000-166973600	Weak transcription	H9 Cell Line	embryonic stem cell
6	chr6:166966000-166974200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
7	chr6:166966200-166971200	Enhancers	Left Ventricle	heart
8	chr6:166966200-166978000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr6:166967000-166971200	Enhancers	Brain Angular Gyrus	brain
10	chr6:166967600-166971000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr6:166967600-166971000	Enhancers	Adipose Nuclei	Adipose
12	chr6:166967600-166971000	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
13	chr6:166967600-166971800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
14	chr6:166968000-166972000	Enhancers	Spleen	Spleen
15	chr6:166968000-166972800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
16	chr6:166968200-166972400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
17	chr6:166968400-166985800	Weak transcription	Fetal Kidney	kidney
18	chr6:166968800-166971000	Enhancers	Breast Myoepithelial Primary Cells	Breast
19	chr6:166968800-166971600	Weak transcription	NHLF	lung
20	chr6:166968800-166973800	Enhancers	HMEC	breast
21	chr6:166969000-166971000	Enhancers	Psoas Muscle	Psoas
22	chr6:166969000-166971000	Enhancers	Right Atrium	heart
23	chr6:166969000-166972400	Enhancers	Fetal Muscle Trunk	muscle
24	chr6:166969000-166973800	Genic enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
25	chr6:166969000-166974000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
26	chr6:166969200-166972200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
27	chr6:166969200-166972200	Enhancers	Esophagus	oesophagus
28	chr6:166969400-166978800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr6:166969600-166971800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
30	chr6:166969800-166971600	Weak transcription	Fetal Stomach	stomach
31	chr6:166969800-166971800	Enhancers	NH-A	brain
32	chr6:166970000-166971000	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
33	chr6:166970000-166971000	Flanking Active TSS	Brain Anterior Caudate	brain
34	chr6:166970000-166971000	Flanking Active TSS	Stomach Smooth Muscle	stomach
35	chr6:166970000-166971000	Enhancers	Hela-S3	cervix
36	chr6:166970000-166971000	Flanking Active TSS	Osteobl	bone
37	chr6:166970000-166971200	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
38	chr6:166970200-166971000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
39	chr6:166970200-166971000	Enhancers	Primary monocytes fromperipheralblood	blood
40	chr6:166970200-166976200	Weak transcription	Right Ventricle	heart
41	chr6:166970400-166971000	Enhancers	H1 Cell Line	embryonic stem cell
42	chr6:166970400-166971000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
43	chr6:166970400-166971000	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
44	chr6:166970400-166971000	Enhancers	Rectal Mucosa Donor 31	rectum
45	chr6:166970400-166971000	Enhancers	Dnd41	blood
46	chr6:166970400-166972400	Enhancers	Skeletal Muscle Female	skeletal muscle
47	chr6:166970400-166972800	Enhancers	Skeletal Muscle Male	skeletal muscle
48	chr6:166970600-166971000	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
49	chr6:166970600-166971000	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
50	chr6:166970600-166971000	Flanking Active TSS	Liver	Liver

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