Variant report

Variant	rs34417240
Chromosome Location	chr19:38529196-38529197
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr19:38514808..38516815-chr19:38528383..38531251,2	MCF-7	breast:

Extended variants
information (count: 15 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs12973690	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12977585	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs12980972	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12980973	0.91[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs34846275	0.91[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs35445607	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs36106417	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs58236040	1.00[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs6508757	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7508583	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs8110656	0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9304573	0.90[EUR][1000 genomes];0.84[ASN][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	nsv949296	chr19:38034722-38763140	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	58 gene(s)	inside rSNPs	diseases
2	nsv911656	chr19:38505037-38539988	Genic enhancers Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv1060359	chr19:38512719-38552438	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	4 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	chr19:38508600-38537000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr19:38514600-38530200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr19:38514800-38537000	Weak transcription	Colonic Mucosa	Colon
4	chr19:38516800-38536200	Weak transcription	Spleen	Spleen
5	chr19:38517000-38530800	Weak transcription	NHEK	skin
6	chr19:38517000-38537000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr19:38521800-38537000	Weak transcription	Esophagus	oesophagus
8	chr19:38521800-38538400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
9	chr19:38521800-38538400	Weak transcription	Sigmoid Colon	Sigmoid Colon
10	chr19:38521800-38548600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chr19:38522000-38536600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
12	chr19:38522000-38553600	Weak transcription	Stomach Smooth Muscle	stomach
13	chr19:38522200-38537200	Weak transcription	Thymus	Thymus
14	chr19:38523400-38529400	Enhancers	Primary hematopoietic stem cells short term culture	blood
15	chr19:38524400-38538400	Weak transcription	Small Intestine	intestine
16	chr19:38525000-38530600	Weak transcription	Pancreatic Islets	Pancreatic Islet
17	chr19:38525000-38540000	Weak transcription	Rectal Mucosa Donor 31	rectum
18	chr19:38525200-38536400	Weak transcription	Primary neutrophils fromperipheralblood	blood
19	chr19:38525200-38536600	Weak transcription	Gastric	stomach
20	chr19:38525800-38537000	Weak transcription	Rectal Mucosa Donor 29	rectum
21	chr19:38525800-38538000	Weak transcription	Duodenum Mucosa	Duodenum
22	chr19:38526000-38537600	Weak transcription	Fetal Intestine Large	intestine
23	chr19:38526200-38529800	Strong transcription	Fetal Intestine Small	intestine
24	chr19:38526800-38545600	Weak transcription	Stomach Mucosa	stomach
25	chr19:38527200-38532600	Weak transcription	GM12878-XiMat	blood
26	chr19:38527200-38534000	Weak transcription	Adipose Nuclei	Adipose
27	chr19:38527400-38529200	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
28	chr19:38527400-38530400	Weak transcription	Osteobl	bone
29	chr19:38527400-38530800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
30	chr19:38527800-38530600	Weak transcription	NHDF-Ad	bronchial
31	chr19:38527800-38530800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
32	chr19:38527800-38532200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr19:38527800-38548800	Weak transcription	Right Atrium	heart
34	chr19:38527800-38551800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
35	chr19:38528000-38530800	Weak transcription	NHLF	lung
36	chr19:38528200-38530800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
37	chr19:38528200-38573200	Weak transcription	Left Ventricle	heart
38	chr19:38528400-38530400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
39	chr19:38528600-38529600	Strong transcription	A549	lung
40	chr19:38528600-38534200	Weak transcription	NH-A	brain
41	chr19:38528600-38538200	Weak transcription	HSMMtube	muscle
42	chr19:38528800-38529200	Enhancers	HSMM	muscle
43	chr19:38528800-38530400	Weak transcription	Muscle Satellite Cultured Cells	--
44	chr19:38528800-38530400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
45	chr19:38528800-38530600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
46	chr19:38528800-38534200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
47	chr19:38528800-38534200	Weak transcription	H9 Cell Line	embryonic stem cell
48	chr19:38528800-38534200	Weak transcription	HUES48 Cell Line	embryonic stem cell
49	chr19:38528800-38534200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
50	chr19:38528800-38534200	Weak transcription	Primary B cells from cord blood	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links