Variant report

Variant	rs60584289
Chromosome Location	chr5:37666202-37666203
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr5:37659630..37663695-chr5:37665450..37669812,5	K562	blood:
2	chr5:37664491..37667181-chr5:37703176..37705396,2	MCF-7	breast:
3	chr5:37661443..37663164-chr5:37664838..37666948,2	MCF-7	breast:

Extended variants
information (count: 49 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs16903702	1.00[AMR][1000 genomes]
rs16903707	1.00[AMR][1000 genomes]
rs16903717	1.00[AMR][1000 genomes]
rs57810602	1.00[AMR][1000 genomes]
rs57947315	1.00[AMR][1000 genomes]
rs59289853	0.84[AFR][1000 genomes]
rs59785719	1.00[AMR][1000 genomes]
rs59975130	1.00[AMR][1000 genomes]
rs60854599	0.84[AFR][1000 genomes]
rs60971228	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs61421708	0.84[AFR][1000 genomes]
rs61573892	1.00[AMR][1000 genomes]
rs6862947	1.00[AMR][1000 genomes]
rs6898181	1.00[AMR][1000 genomes]
rs73061728	1.00[AMR][1000 genomes]
rs73061742	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73061751	1.00[AMR][1000 genomes]
rs73061771	1.00[AMR][1000 genomes]
rs73061776	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73061780	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73063791	1.00[AFR][1000 genomes]
rs73063799	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73063800	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73065617	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73065632	1.00[AMR][1000 genomes]
rs73065634	1.00[AMR][1000 genomes]
rs73065654	1.00[AMR][1000 genomes]
rs73067718	1.00[AMR][1000 genomes]
rs73067721	1.00[AMR][1000 genomes]
rs73067725	1.00[AMR][1000 genomes]
rs73067728	1.00[AMR][1000 genomes]
rs73074108	0.84[AFR][1000 genomes]
rs73074115	0.84[AFR][1000 genomes]
rs7704010	1.00[AMR][1000 genomes]
rs7724612	1.00[AMR][1000 genomes]
rs9686445	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:13 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1026554	chr5:37112133-37734859	Strong transcription Weak transcription Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	45 gene(s)	inside rSNPs	diseases
2	nsv537726	chr5:37112133-37734859	Weak transcription Strong transcription Enhancers Active TSS Genic enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	45 gene(s)	inside rSNPs	diseases
3	nsv949716	chr5:37179341-37967352	Weak transcription Strong transcription Flanking Active TSS Enhancers Bivalent Enhancer Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	58 gene(s)	inside rSNPs	diseases
4	nsv1015983	chr5:37240827-37666601	Strong transcription Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	40 gene(s)	inside rSNPs	diseases
5	nsv1023871	chr5:37330018-37804744	Enhancers Strong transcription Weak transcription Active TSS ZNF genes & repeats Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
6	nsv537729	chr5:37330018-37804744	Weak transcription Flanking Active TSS Strong transcription Genic enhancers Enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
7	nsv432744	chr5:37374124-37743077	ZNF genes & repeats Strong transcription Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
8	nsv1034094	chr5:37406859-37666704	Weak transcription ZNF genes & repeats Strong transcription Enhancers Flanking Active TSS Genic enhancers Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
9	nsv537731	chr5:37406859-37666704	ZNF genes & repeats Strong transcription Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
10	nsv597846	chr5:37430215-37813591	Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
11	nsv880890	chr5:37443079-37681646	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
12	nsv1030250	chr5:37478163-37734859	ZNF genes & repeats Enhancers Weak transcription Strong transcription Active TSS Genic enhancers Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
13	nsv881383	chr5:37485316-37773877	Strong transcription Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:71 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:37654600-37671800	Weak transcription	Primary T cells from cord blood	blood
2	chr5:37656600-37671600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr5:37658800-37667400	Weak transcription	Hela-S3	cervix
4	chr5:37659000-37668000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
5	chr5:37659000-37668000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr5:37659000-37668600	Weak transcription	HUES6 Cell Line	embryonic stem cell
7	chr5:37662600-37668200	Weak transcription	Placenta Amnion	Placenta Amnion
8	chr5:37662800-37667200	Weak transcription	Pancreatic Islets	Pancreatic Islet
9	chr5:37662800-37671800	Weak transcription	Small Intestine	intestine
10	chr5:37663000-37667600	Weak transcription	HepG2	liver
11	chr5:37663400-37666400	Weak transcription	A549	lung
12	chr5:37664000-37667800	Weak transcription	Fetal Intestine Small	intestine
13	chr5:37664000-37668600	Weak transcription	HUES48 Cell Line	embryonic stem cell
14	chr5:37664000-37668600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
15	chr5:37664000-37671800	Weak transcription	Primary hematopoietic stem cells	blood
16	chr5:37664400-37667400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
17	chr5:37664400-37667400	Weak transcription	Osteobl	bone
18	chr5:37664400-37668000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr5:37664400-37668400	Weak transcription	HUES64 Cell Line	embryonic stem cell
20	chr5:37664600-37668200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
21	chr5:37664800-37667600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
22	chr5:37665000-37666800	Enhancers	Breast Myoepithelial Primary Cells	Breast
23	chr5:37665000-37668600	Weak transcription	Primary neutrophils fromperipheralblood	blood
24	chr5:37665200-37666400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
25	chr5:37665200-37666600	Enhancers	Fetal Heart	heart
26	chr5:37665200-37668600	Enhancers	Rectal Smooth Muscle	rectum
27	chr5:37665400-37666400	Enhancers	Brain Hippocampus Middle	brain
28	chr5:37665400-37666400	Enhancers	Placenta	Placenta
29	chr5:37665400-37666400	Enhancers	Spleen	Spleen
30	chr5:37665400-37666800	Enhancers	Ovary	ovary
31	chr5:37665400-37666800	Enhancers	Psoas Muscle	Psoas
32	chr5:37665400-37666800	Enhancers	Right Atrium	heart
33	chr5:37665400-37666800	Enhancers	HSMM	muscle
34	chr5:37665400-37667000	Enhancers	Brain Anterior Caudate	brain
35	chr5:37665400-37667000	Enhancers	Duodenum Mucosa	Duodenum
36	chr5:37665400-37667000	Enhancers	Fetal Muscle Leg	muscle
37	chr5:37665400-37667000	Enhancers	Pancreas	Pancrea
38	chr5:37665400-37667000	Enhancers	Sigmoid Colon	Sigmoid Colon
39	chr5:37665400-37667000	Enhancers	HSMMtube	muscle
40	chr5:37665400-37667200	Enhancers	Aorta	Aorta
41	chr5:37665400-37667400	Enhancers	Fetal Stomach	stomach
42	chr5:37665400-37667800	Enhancers	Fetal Lung	lung
43	chr5:37665400-37667800	Enhancers	Skeletal Muscle Female	skeletal muscle
44	chr5:37665400-37669400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
45	chr5:37665400-37669800	Enhancers	NHLF	lung
46	chr5:37665600-37666400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
47	chr5:37665600-37666400	Enhancers	Left Ventricle	heart
48	chr5:37665600-37667200	Enhancers	NHDF-Ad	bronchial
49	chr5:37665600-37669200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
50	chr5:37665800-37666400	Flanking Active TSS	Brain Substantia Nigra	brain

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links