Variant report

Variant	rs7666972
Chromosome Location	chr4:22470040-22470041
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr4:22466667..22470398-chr4:22474006..22476709,3	MCF-7	breast:

Variant related genes	Relation type
ENSG00000152990	Chromatin interaction

Extended variants
information (count: 39 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:36)

rs_ID	r²[population]
rs11932316	1.00[AMR][1000 genomes]
rs56029242	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs56383378	0.96[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs56965161	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs57310135	0.92[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs58098085	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59383860	1.00[EUR][1000 genomes]
rs61574687	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs61588486	0.85[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs61793366	0.89[AFR][1000 genomes]
rs61793367	0.89[AFR][1000 genomes]
rs6812519	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73800932	1.00[EUR][1000 genomes]
rs73800934	1.00[EUR][1000 genomes]
rs73800935	1.00[EUR][1000 genomes]
rs73800940	1.00[EUR][1000 genomes]
rs73800946	1.00[EUR][1000 genomes]
rs73800949	1.00[EUR][1000 genomes]
rs73800956	1.00[EUR][1000 genomes]
rs73800958	0.85[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs73800959	0.85[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs73800963	0.89[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs73800964	0.92[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs73802816	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73802817	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73802819	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73802821	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73802824	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73802827	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs73802829	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73802830	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73802831	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73802832	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73802835	1.00[AMR][1000 genomes]
rs73802836	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7666836	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[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	esv3349061	chr4:22379581-22887563	Enhancers Weak transcription Strong transcription Active TSS Genic enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
2	nsv878752	chr4:22414023-22501043	Enhancers Flanking Active TSS Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
3	nsv821634	chr4:22427074-22865948	Enhancers Weak transcription Active TSS Strong transcription Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 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	chr4:22388400-22473600	Weak transcription	Rectal Smooth Muscle	rectum
2	chr4:22389200-22473600	Weak transcription	Fetal Brain Male	brain
3	chr4:22419200-22476200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
4	chr4:22420600-22488000	Weak transcription	Aorta	Aorta
5	chr4:22433800-22479200	Weak transcription	Brain Hippocampus Middle	brain
6	chr4:22437400-22476400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
7	chr4:22443400-22471200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
8	chr4:22443400-22472400	Weak transcription	Ovary	ovary
9	chr4:22443400-22473600	Weak transcription	Fetal Brain Female	brain
10	chr4:22443600-22470800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
11	chr4:22443600-22476200	Weak transcription	A549	lung
12	chr4:22443800-22474600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr4:22444000-22470800	Weak transcription	Cortex derived primary cultured neurospheres	brain
14	chr4:22447200-22473800	Weak transcription	Stomach Smooth Muscle	stomach
15	chr4:22447200-22475000	Weak transcription	NHLF	lung
16	chr4:22447800-22473400	Weak transcription	Brain Germinal Matrix	brain
17	chr4:22448600-22472600	Weak transcription	Primary T cells from cord blood	blood
18	chr4:22450200-22471000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
19	chr4:22450200-22473800	Weak transcription	Primary hematopoietic stem cells	blood
20	chr4:22450200-22473800	Weak transcription	NH-A	brain
21	chr4:22450400-22474800	Weak transcription	Adipose Nuclei	Adipose
22	chr4:22450400-22476000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
23	chr4:22450400-22484000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
24	chr4:22450400-22493200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr4:22455600-22474200	Weak transcription	Fetal Thymus	thymus
26	chr4:22456400-22476200	Weak transcription	H9 Cell Line	embryonic stem cell
27	chr4:22456800-22476000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
28	chr4:22456800-22479000	Weak transcription	Duodenum Mucosa	Duodenum
29	chr4:22456800-22485000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
30	chr4:22457000-22473600	Weak transcription	Colon Smooth Muscle	Colon
31	chr4:22457200-22473400	Weak transcription	Duodenum Smooth Muscle	Duodenum
32	chr4:22457200-22473800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
33	chr4:22457600-22473600	Weak transcription	Fetal Lung	lung
34	chr4:22458200-22472200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
35	chr4:22458400-22472000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
36	chr4:22460200-22472400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
37	chr4:22460400-22470800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
38	chr4:22460400-22471000	Weak transcription	Psoas Muscle	Psoas
39	chr4:22460400-22472000	Weak transcription	HSMMtube	muscle
40	chr4:22460400-22472400	Weak transcription	Pancreas	Pancrea
41	chr4:22460400-22472600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
42	chr4:22461200-22471400	Weak transcription	HUES6 Cell Line	embryonic stem cell
43	chr4:22461800-22472400	Weak transcription	Lung	lung
44	chr4:22462000-22493200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
45	chr4:22462200-22470800	Weak transcription	NHEK	skin
46	chr4:22462400-22471000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
47	chr4:22462400-22483600	Weak transcription	Liver	Liver
48	chr4:22462600-22471800	Weak transcription	Sigmoid Colon	Sigmoid Colon
49	chr4:22462600-22472200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
50	chr4:22462600-22472400	Weak transcription	Gastric	stomach

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