Variant report

Variant	rs72664891
Chromosome Location	chr1:61739556-61739557
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:61734323..61736930-chr1:61738925..61740975,2	MCF-7	breast:
2	chr1:61737048..61738584-chr1:61739343..61741335,2	K562	blood:

Extended variants
information (count: 27 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs11207719	0.96[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1977653	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2275208	0.85[EUR][1000 genomes]
rs333136	0.89[EUR][1000 genomes]
rs333138	0.85[EUR][1000 genomes]
rs333140	0.89[EUR][1000 genomes]
rs333141	0.89[EUR][1000 genomes]
rs333142	0.89[EUR][1000 genomes]
rs333144	0.87[EUR][1000 genomes]
rs333145	0.83[EUR][1000 genomes]
rs333147	0.83[EUR][1000 genomes]
rs333150	0.85[EUR][1000 genomes]
rs333165	0.85[EUR][1000 genomes]
rs333166	0.85[EUR][1000 genomes]
rs334690	0.85[EUR][1000 genomes]
rs6684051	0.96[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs72664877	0.85[EUR][1000 genomes]
rs72664888	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs72664890	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv994970	chr1:61693951-62199657	Strong transcription Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
2	nsv1006142	chr1:61696142-62119763	Enhancers Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
3	nsv534980	chr1:61696142-62119763	Enhancers Flanking Active TSS Active TSS Strong transcription Weak transcription Bivalent Enhancer Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
4	nsv916868	chr1:61700430-62119762	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
5	nsv1001052	chr1:61702011-62090670	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	3 gene(s)	inside rSNPs	diseases
6	nsv817402	chr1:61703965-62119762	Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
7	nsv1010797	chr1:61703966-62125970	Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Strong transcription Active TSS Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
8	nsv530494	chr1:61723918-62084045	Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	3 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:61720800-61755800	Weak transcription	Fetal Intestine Small	intestine
2	chr1:61721000-61754400	Weak transcription	Pancreas	Pancrea
3	chr1:61722800-61740600	Weak transcription	Stomach Smooth Muscle	stomach
4	chr1:61725800-61750400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
5	chr1:61726000-61742800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
6	chr1:61726000-61743200	Weak transcription	Fetal Muscle Leg	muscle
7	chr1:61728000-61740600	Weak transcription	Duodenum Smooth Muscle	Duodenum
8	chr1:61729200-61742000	Weak transcription	Skeletal Muscle Male	skeletal muscle
9	chr1:61729600-61754400	Weak transcription	Lung	lung
10	chr1:61732600-61742800	Weak transcription	Muscle Satellite Cultured Cells	--
11	chr1:61732800-61750000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr1:61735600-61740600	Weak transcription	Liver	Liver
13	chr1:61735600-61742000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
14	chr1:61735600-61743200	Weak transcription	Fetal Stomach	stomach
15	chr1:61735800-61742000	Weak transcription	HUES6 Cell Line	embryonic stem cell
16	chr1:61735800-61742000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
17	chr1:61737000-61750000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
18	chr1:61737200-61742000	Weak transcription	HUES64 Cell Line	embryonic stem cell
19	chr1:61737200-61742000	Weak transcription	Fetal Heart	heart
20	chr1:61737200-61751600	Weak transcription	Hela-S3	cervix
21	chr1:61737400-61740400	Weak transcription	Fetal Brain Female	brain
22	chr1:61737400-61741800	Weak transcription	A549	lung
23	chr1:61737400-61747600	Weak transcription	HepG2	liver
24	chr1:61737400-61750000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
25	chr1:61737400-61751800	Weak transcription	Esophagus	oesophagus
26	chr1:61737600-61739800	Enhancers	K562	blood
27	chr1:61737600-61750200	Weak transcription	NHEK	skin
28	chr1:61738000-61740400	Enhancers	Brain Germinal Matrix	brain
29	chr1:61738000-61752600	Weak transcription	HUVEC	blood vessel
30	chr1:61738200-61740200	Enhancers	Brain Anterior Caudate	brain
31	chr1:61738200-61740800	Enhancers	Brain Cingulate Gyrus	brain
32	chr1:61738400-61740800	Enhancers	Brain Substantia Nigra	brain
33	chr1:61738800-61739800	Enhancers	Brain Angular Gyrus	brain
34	chr1:61738800-61740200	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
35	chr1:61738800-61740400	Enhancers	Aorta	Aorta
36	chr1:61738800-61741200	Enhancers	Cortex derived primary cultured neurospheres	brain
37	chr1:61738800-61741200	Enhancers	Adipose Nuclei	Adipose
38	chr1:61739000-61739800	Enhancers	Psoas Muscle	Psoas
39	chr1:61739000-61740000	Enhancers	Brain Inferior Temporal Lobe	brain
40	chr1:61739000-61740800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
41	chr1:61739000-61746200	Enhancers	Fetal Brain Male	brain
42	chr1:61739200-61739800	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
43	chr1:61739200-61739800	Enhancers	Colon Smooth Muscle	Colon
44	chr1:61739200-61740200	Weak transcription	Fetal Lung	lung
45	chr1:61739200-61742800	Weak transcription	Left Ventricle	heart
46	chr1:61739400-61739800	Weak transcription	Rectal Smooth Muscle	rectum
47	chr1:61739400-61740400	Enhancers	Brain Hippocampus Middle	brain
48	chr1:61739400-61740600	Weak transcription	Right Atrium	heart
49	chr1:61739400-61740600	Weak transcription	Skeletal Muscle Female	skeletal muscle
50	chr1:61739400-61745400	Weak transcription	Small Intestine	intestine

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