Variant report

Variant	rs9389985
Chromosome Location	chr6:142653898-142653899
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr6:142648503..142651872-chr6:142652500..142656138,3	MCF-7	breast:
2	chr6:142644240..142648928-chr6:142651290..142656139,5	MCF-7	breast:
3	chr6:142653598..142655313-chr6:142655827..142657929,2	K562	blood:

Extended variants
information (count: 61 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:59)

rs_ID	r²[population]
rs1040525	0.95[CHB][hapmap];1.00[JPT][hapmap];0.93[AMR][1000 genomes];0.92[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1040526	0.94[CEU][hapmap];0.95[CHB][hapmap];0.86[AMR][1000 genomes];0.90[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1342060	0.81[CEU][hapmap];0.85[CHB][hapmap];0.82[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs1360194	0.94[CEU][hapmap];0.95[CHB][hapmap];0.86[AMR][1000 genomes];0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1418201	0.94[CEU][hapmap];0.91[CHB][hapmap];1.00[JPT][hapmap];0.81[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs155259	0.81[EUR][1000 genomes]
rs1891308	0.81[CEU][hapmap];0.90[CHB][hapmap];1.00[JPT][hapmap];0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2039986	0.94[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2039987	1.00[CEU][hapmap];0.86[CHB][hapmap];0.94[EUR][1000 genomes]
rs2050157	0.81[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2294764	0.94[CEU][hapmap];0.90[CHB][hapmap];0.86[AMR][1000 genomes];0.90[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2294771	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs262119	0.81[EUR][1000 genomes]
rs262121	0.81[EUR][1000 genomes]
rs262129	0.81[EUR][1000 genomes]
rs263180	0.81[EUR][1000 genomes]
rs263181	0.81[EUR][1000 genomes]
rs263182	0.81[EUR][1000 genomes]
rs263183	0.81[EUR][1000 genomes]
rs263184	0.81[EUR][1000 genomes]
rs263186	0.81[EUR][1000 genomes]
rs263187	0.81[EUR][1000 genomes]
rs263188	0.81[EUR][1000 genomes]
rs263189	0.81[EUR][1000 genomes]
rs3748069	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs3817929	0.83[CEU][hapmap];0.95[CHB][hapmap];0.82[JPT][hapmap];0.85[AMR][1000 genomes];0.89[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4896582	0.81[CEU][hapmap];0.87[EUR][1000 genomes]
rs6570507	0.81[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6570508	0.85[EUR][1000 genomes]
rs6570509	0.87[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6570510	0.90[CHB][hapmap];0.86[AMR][1000 genomes];0.89[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs6909857	0.93[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6929442	0.87[CEU][hapmap];0.90[CHB][hapmap];0.81[JPT][hapmap];0.85[AMR][1000 genomes];0.89[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6937121	0.94[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7741741	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7753012	0.83[CEU][hapmap]
rs7754638	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7755109	0.88[CEU][hapmap];0.95[CHB][hapmap];0.85[AMR][1000 genomes];0.89[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7756305	0.81[CEU][hapmap];0.85[CHB][hapmap];0.93[EUR][1000 genomes]
rs7763064	0.86[EUR][1000 genomes]
rs7770386	0.89[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7774095	0.90[CHB][hapmap];0.86[AMR][1000 genomes];0.96[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7776375	0.85[AMR][1000 genomes];0.88[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs9373346	0.81[CEU][hapmap];0.90[CHB][hapmap];0.82[JPT][hapmap];0.90[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs9389984	0.94[EUR][1000 genomes]
rs9389986	0.81[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.83[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9389987	0.92[EUR][1000 genomes]
rs9399401	0.81[CEU][hapmap];0.86[CHB][hapmap];0.92[EUR][1000 genomes]
rs9403380	0.80[AFR][1000 genomes];0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9403381	0.81[CEU][hapmap];0.85[CHB][hapmap];0.87[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs9403382	0.82[AFR][1000 genomes];0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9403383	0.95[CHB][hapmap];1.00[JPT][hapmap];0.81[AFR][1000 genomes];0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9403387	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs9496346	0.87[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9496369	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9496374	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs9496392	0.87[EUR][1000 genomes]
rs962554	0.88[CEU][hapmap];0.95[CHB][hapmap];0.86[AMR][1000 genomes];0.91[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs972982	0.81[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv949088	chr6:142561402-143128849	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
2	nsv830825	chr6:142585242-142752575	Enhancers Weak transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:26 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:142649000-142655400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
2	chr6:142650600-142654200	Enhancers	HMEC	breast
3	chr6:142650800-142654200	Enhancers	Fetal Lung	lung
4	chr6:142650800-142654600	Enhancers	NHLF	lung
5	chr6:142651000-142654600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr6:142651000-142656600	Enhancers	Liver	Liver
7	chr6:142651200-142654400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr6:142651400-142654800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
9	chr6:142651800-142654000	Enhancers	HUES64 Cell Line	embryonic stem cell
10	chr6:142652400-142654200	Enhancers	Primary hematopoietic stem cells	blood
11	chr6:142652600-142656600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
12	chr6:142652800-142654000	Weak transcription	HUES6 Cell Line	embryonic stem cell
13	chr6:142653000-142654200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
14	chr6:142653000-142656000	Enhancers	HUVEC	blood vessel
15	chr6:142653000-142660800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
16	chr6:142653200-142657200	Enhancers	HepG2	liver
17	chr6:142653600-142654000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
18	chr6:142653600-142654000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
19	chr6:142653600-142654400	Enhancers	NHEK	skin
20	chr6:142653800-142654000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr6:142653800-142654000	Genic enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
22	chr6:142653800-142654400	Enhancers	Fetal Heart	heart
23	chr6:142653800-142654600	Genic enhancers	A549	lung
24	chr6:142653800-142654800	Genic enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
25	chr6:142653800-142654800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr6:142653800-142656400	Weak transcription	ES-I3 Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links