Variant report

Variant	rs34541555
Chromosome Location	chr9:117957723-117957724
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr9:117953158..117955908-chr9:117957675..117960563,2	MCF-7	breast:

Extended variants
information (count: 23 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10982595	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs10982604	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10982606	0.83[AFR][1000 genomes];0.93[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs10982609	0.83[AFR][1000 genomes];0.93[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs1110169	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12379021	0.83[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12682693	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs13292941	0.83[AFR][1000 genomes];0.92[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs1537732	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs17244791	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1888672	0.96[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1888673	0.84[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2183702	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs4147052	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs4978628	0.84[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6478145	0.89[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6478149	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7860900	0.88[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7866181	0.87[EUR][1000 genomes];0.87[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv615250	chr9:117768021-118012841	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv916912	chr9:117770039-118014140	Flanking Active TSS Enhancers Strong transcription Genic enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv831697	chr9:117860416-118023927	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Genic enhancers Strong transcription 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	4 gene(s)	inside rSNPs	diseases
4	nsv893769	chr9:117936903-117985886	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:27 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:117930000-117964400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr9:117945600-117959400	Weak transcription	Fetal Kidney	kidney
3	chr9:117945800-117959600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr9:117954600-117959400	Weak transcription	Rectal Smooth Muscle	rectum
5	chr9:117955600-117959000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr9:117955600-117959400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
7	chr9:117955600-117960200	Weak transcription	Stomach Smooth Muscle	stomach
8	chr9:117955600-117960400	Weak transcription	Fetal Stomach	stomach
9	chr9:117955600-117960400	Weak transcription	Spleen	Spleen
10	chr9:117955600-117969000	Weak transcription	H9 Cell Line	embryonic stem cell
11	chr9:117955800-117960200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
12	chr9:117956600-117958400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr9:117956600-117959400	Weak transcription	Cortex derived primary cultured neurospheres	brain
14	chr9:117956800-117959000	Weak transcription	Fetal Muscle Leg	muscle
15	chr9:117956800-117960000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
16	chr9:117957000-117958200	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
17	chr9:117957000-117960000	Weak transcription	NHLF	lung
18	chr9:117957000-117960200	Weak transcription	NH-A	brain
19	chr9:117957000-117962800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
20	chr9:117957200-117959800	Weak transcription	Osteobl	bone
21	chr9:117957400-117959400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr9:117957400-117959600	Weak transcription	Colon Smooth Muscle	Colon
23	chr9:117957400-117959600	Weak transcription	Fetal Lung	lung
24	chr9:117957400-117959800	Weak transcription	NHDF-Ad	bronchial
25	chr9:117957400-117960000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
26	chr9:117957400-117960400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
27	chr9:117957600-117960200	Weak transcription	HUES64 Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links