Variant report

Variant	rs73167633
Chromosome Location	chr7:150666697-150666698
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	chr7:150661035..150665420-chr7:150665668..150673641,9	MCF-7	breast:

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

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs17173664	0.86[EUR][1000 genomes]
rs36210421	0.88[EUR][1000 genomes]
rs41307316	0.97[EUR][1000 genomes]
rs41308978	0.97[EUR][1000 genomes]
rs41308993	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs41309017	0.84[EUR][1000 genomes]
rs41309026	0.84[EUR][1000 genomes]
rs55642626	0.94[EUR][1000 genomes]
rs55813292	0.82[EUR][1000 genomes]
rs73167606	0.89[EUR][1000 genomes]
rs73167607	0.86[EUR][1000 genomes]
rs73167609	0.86[EUR][1000 genomes]
rs73167611	0.86[EUR][1000 genomes]
rs73167612	0.84[EUR][1000 genomes]
rs73167614	0.86[EUR][1000 genomes]
rs73167615	0.86[EUR][1000 genomes]
rs73167623	0.97[EUR][1000 genomes]
rs73167625	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73167627	0.95[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7792983	0.84[AFR][1000 genomes];0.89[AMR][1000 genomes];0.94[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:19 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv608990	chr7:149961274-150707488	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Weak transcription ZNF genes & repeats Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	90 gene(s)	inside rSNPs	diseases
2	nsv1030109	chr7:150312916-150701010	Enhancers Active TSS Weak transcription Bivalent Enhancer ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
3	esv1821419	chr7:150593315-150974269	Enhancers Strong transcription Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	128 gene(s)	inside rSNPs	diseases
4	nsv465212	chr7:150598492-150667210	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region miRNA target site	12 gene(s)	inside rSNPs	diseases
5	nsv609000	chr7:150598492-150667210	Genic enhancers Bivalent Enhancer Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region miRNA target site	12 gene(s)	inside rSNPs	diseases
6	nsv465213	chr7:150606288-150667210	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region miRNA target site	12 gene(s)	inside rSNPs	diseases
7	nsv609001	chr7:150606288-150667210	Enhancers Weak transcription Bivalent Enhancer Strong transcription ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region miRNA target site	12 gene(s)	inside rSNPs	diseases
8	nsv1022246	chr7:150619660-150779924	Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Genic enhancers Enhancers Weak transcription Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	52 gene(s)	inside rSNPs	diseases
9	nsv889463	chr7:150640285-150700946	Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Bivalent/Poised TSS Weak transcription Bivalent Enhancer Genic enhancers Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region miRNA target site	20 gene(s)	inside rSNPs	diseases
10	nsv889464	chr7:150640285-150723467	Enhancers Active TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
11	nsv889465	chr7:150640285-150800823	Flanking Active TSS Strong transcription Enhancers Flanking Bivalent TSS/Enh Genic enhancers Weak transcription Bivalent Enhancer Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	59 gene(s)	inside rSNPs	diseases
12	nsv889466	chr7:150642341-150687430	Enhancers Bivalent Enhancer Active TSS Genic enhancers Bivalent/Poised TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	19 gene(s)	inside rSNPs	diseases
13	nsv1017863	chr7:150643928-150779924	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	52 gene(s)	inside rSNPs	diseases
14	nsv539197	chr7:150643928-150779924	Bivalent/Poised TSS Active TSS Strong transcription Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Genic enhancers Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	52 gene(s)	inside rSNPs	diseases
15	nsv1028645	chr7:150643928-150806534	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Active TSS Strong transcription Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	59 gene(s)	inside rSNPs	diseases
16	nsv539198	chr7:150643928-150879259	Weak transcription Enhancers Flanking Bivalent TSS/Enh Genic enhancers Flanking Active TSS Bivalent Enhancer Strong transcription Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	72 gene(s)	inside rSNPs	diseases
17	nsv889467	chr7:150645534-150723467	Weak transcription Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
18	nsv889468	chr7:150652419-150696111	Weak transcription Flanking Bivalent TSS/Enh Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	20 gene(s)	inside rSNPs	diseases
19	nsv889469	chr7:150657209-150747746	Flanking Bivalent TSS/Enh Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Strong transcription Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:150657200-150669600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
2	chr7:150658200-150670800	Enhancers	Rectal Smooth Muscle	rectum
3	chr7:150658800-150670400	Enhancers	Duodenum Smooth Muscle	Duodenum
4	chr7:150660200-150668200	Weak transcription	Brain Inferior Temporal Lobe	brain
5	chr7:150660400-150668000	Weak transcription	Brain Substantia Nigra	brain
6	chr7:150660600-150666800	Weak transcription	HUES64 Cell Line	embryonic stem cell
7	chr7:150661800-150670400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
8	chr7:150662600-150667400	Weak transcription	Spleen	Spleen
9	chr7:150663400-150668200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr7:150664000-150670000	Weak transcription	Pancreatic Islets	Pancreatic Islet
11	chr7:150664400-150673600	Enhancers	Fetal Lung	lung
12	chr7:150664600-150674000	Enhancers	Fetal Brain Male	brain
13	chr7:150665200-150667200	Enhancers	K562	blood
14	chr7:150665200-150671800	Genic enhancers	Fetal Stomach	stomach
15	chr7:150665400-150667200	Flanking Active TSS	Stomach Smooth Muscle	stomach
16	chr7:150665400-150667200	Enhancers	HSMMtube	muscle
17	chr7:150665400-150668400	Bivalent Enhancer	Placenta	Placenta
18	chr7:150665400-150671800	Enhancers	Left Ventricle	heart
19	chr7:150665600-150667800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
20	chr7:150665600-150669800	Enhancers	Fetal Brain Female	brain
21	chr7:150665600-150671200	Enhancers	Right Ventricle	heart
22	chr7:150665800-150666800	Enhancers	Primary T helper cells fromperipheralblood	blood
23	chr7:150665800-150666800	Weak transcription	Fetal Intestine Large	intestine
24	chr7:150665800-150666800	Bivalent Enhancer	Fetal Muscle Leg	muscle
25	chr7:150665800-150666800	Enhancers	Lung	lung
26	chr7:150665800-150669200	Enhancers	H1 Cell Line	embryonic stem cell
27	chr7:150665800-150669200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
28	chr7:150665800-150669600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
29	chr7:150666000-150666800	Enhancers	Brain Anterior Caudate	brain
30	chr7:150666000-150666800	Enhancers	Right Atrium	heart
31	chr7:150666000-150667000	Flanking Active TSS	Colon Smooth Muscle	Colon
32	chr7:150666000-150667200	Enhancers	iPS-15b Cell Line	embryonic stem cell
33	chr7:150666000-150667200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
34	chr7:150666000-150668600	Enhancers	Brain Germinal Matrix	brain
35	chr7:150666000-150668800	Enhancers	iPS-18 Cell Line	embryonic stem cell
36	chr7:150666000-150669600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr7:150666000-150669600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr7:150666000-150670200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
39	chr7:150666000-150670400	Enhancers	Fetal Intestine Small	intestine
40	chr7:150666200-150667000	Enhancers	Brain Hippocampus Middle	brain
41	chr7:150666200-150667200	Flanking Active TSS	Fetal Heart	heart
42	chr7:150666200-150667800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
43	chr7:150666200-150668400	Enhancers	iPS-20b Cell Line	embryonic stem cell
44	chr7:150666200-150669800	Enhancers	Ovary	ovary
45	chr7:150666200-150670000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
46	chr7:150666200-150670800	Enhancers	Cortex derived primary cultured neurospheres	brain
47	chr7:150666400-150667000	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
48	chr7:150666400-150667000	Bivalent Enhancer	Skeletal Muscle Female	skeletal muscle
49	chr7:150666400-150667200	Enhancers	Brain Cingulate Gyrus	brain
50	chr7:150666400-150667200	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain

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