Variant report

Variant	rs7043705
Chromosome Location	chr9:97791295-97791296
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr9:97678393..97680086-chr9:97790321..97791837,2	MCF-7	breast:
2	chr9:97626084..97627897-chr9:97790026..97791698,2	MCF-7	breast:
3	chr9:97791289..97793582-chr9:97853696..97856435,2	MCF-7	breast:
4	chr9:97785037..97786966-chr9:97789243..97791413,3	MCF-7	breast:
5	chr9:97790920..97793019-chr9:97799346..97801505,2	K562	blood:

Extended variants
information (count: 61 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:60)

rs_ID	r²[population]
rs1004373	0.84[AMR][1000 genomes];0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10117370	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10119512	0.84[AMR][1000 genomes];0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10121760	0.82[AMR][1000 genomes];0.90[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10123819	0.84[AMR][1000 genomes];0.90[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1020963	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs10512253	0.84[AMR][1000 genomes];0.90[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10761364	0.84[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10761366	0.88[AMR][1000 genomes];0.99[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs10761368	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs10761369	0.91[EUR][1000 genomes]
rs10993427	0.82[AMR][1000 genomes];0.85[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10993464	0.84[AMR][1000 genomes];0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10993467	0.84[AMR][1000 genomes];0.90[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1113102	0.88[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1412488	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.92[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs1564234	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1571894	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1571895	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2061800	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2404305	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2404456	0.84[AMR][1000 genomes];0.85[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs3802454	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs3802456	0.84[AMR][1000 genomes];0.96[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs3858089	0.85[ASN][1000 genomes]
rs4537362	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4743979	0.84[AMR][1000 genomes];0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4743980	0.84[AMR][1000 genomes];0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4743981	0.88[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs4743982	0.84[AMR][1000 genomes];0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4743984	0.84[AMR][1000 genomes];0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4744422	0.96[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs4744423	0.84[AMR][1000 genomes];0.96[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4744424	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4744425	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4744426	0.84[AMR][1000 genomes];0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4744428	0.84[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs4744430	0.84[AMR][1000 genomes];0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4744431	0.84[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs4744432	0.84[AMR][1000 genomes];0.90[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4744433	0.84[AMR][1000 genomes];0.90[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4744435	0.88[EUR][1000 genomes]
rs6479588	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs6479591	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6479592	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7020709	0.86[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7021351	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7022452	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7048786	0.84[AMR][1000 genomes];0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7048941	0.84[AMR][1000 genomes];0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7851173	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7854831	0.86[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7857679	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7862156	0.84[AMR][1000 genomes];0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7863291	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7865144	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7871218	0.81[AMR][1000 genomes];0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7873479	0.96[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs7873567	0.88[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs962229	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv933919	chr9:97619512-97919344	Weak transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	293 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs7043705	hCG_2003663	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:91 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:97770800-97810000	Weak transcription	Primary T cells from cord blood	blood
2	chr9:97773200-97793200	Weak transcription	Brain Germinal Matrix	brain
3	chr9:97777400-97794200	Weak transcription	Thymus	Thymus
4	chr9:97781200-97793600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
5	chr9:97781400-97793200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr9:97781400-97793600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr9:97782000-97792800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
8	chr9:97782600-97793600	Weak transcription	Primary hematopoietic stem cells	blood
9	chr9:97783600-97794000	Weak transcription	GM12878-XiMat	blood
10	chr9:97786200-97791800	Enhancers	Right Ventricle	heart
11	chr9:97787000-97794000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
12	chr9:97787600-97793000	Genic enhancers	HepG2	liver
13	chr9:97787800-97792800	Weak transcription	Spleen	Spleen
14	chr9:97787800-97793800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
15	chr9:97787800-97795800	Genic enhancers	Osteobl	bone
16	chr9:97788000-97794800	Genic enhancers	Muscle Satellite Cultured Cells	--
17	chr9:97788200-97792800	Weak transcription	Cortex derived primary cultured neurospheres	brain
18	chr9:97788200-97793000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
19	chr9:97788200-97794400	Weak transcription	K562	blood
20	chr9:97788400-97795800	Genic enhancers	Breast Myoepithelial Primary Cells	Breast
21	chr9:97788800-97792200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
22	chr9:97788800-97792800	Weak transcription	Adipose Nuclei	Adipose
23	chr9:97788800-97795000	Weak transcription	Placenta Amnion	Placenta Amnion
24	chr9:97788800-97795800	Enhancers	Psoas Muscle	Psoas
25	chr9:97789000-97791400	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
26	chr9:97789000-97793000	Weak transcription	Aorta	Aorta
27	chr9:97789000-97793000	Weak transcription	HUVEC	blood vessel
28	chr9:97789000-97794200	Genic enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
29	chr9:97789000-97794400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
30	chr9:97789000-97806200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
31	chr9:97789200-97791400	Weak transcription	Fetal Kidney	kidney
32	chr9:97789200-97791400	Weak transcription	Small Intestine	intestine
33	chr9:97789800-97791600	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
34	chr9:97789800-97792400	Enhancers	Fetal Lung	lung
35	chr9:97789800-97792800	Enhancers	Brain Substantia Nigra	brain
36	chr9:97789800-97792800	Enhancers	Fetal Heart	heart
37	chr9:97790000-97792000	Genic enhancers	NHEK	skin
38	chr9:97790000-97792200	Transcr. at gene 5' and 3'	A549	lung
39	chr9:97790000-97794400	Genic enhancers	NH-A	brain
40	chr9:97790000-97795800	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
41	chr9:97790000-97796800	Genic enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
42	chr9:97790200-97791400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr9:97790200-97791400	Genic enhancers	NHLF	lung
44	chr9:97790200-97791600	Genic enhancers	Rectal Mucosa Donor 29	rectum
45	chr9:97790200-97791600	Transcr. at gene 5' and 3'	Skeletal Muscle Male	skeletal muscle
46	chr9:97790200-97791800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
47	chr9:97790200-97791800	Genic enhancers	Colon Smooth Muscle	Colon
48	chr9:97790200-97791800	Enhancers	Gastric	stomach
49	chr9:97790200-97791800	Enhancers	Stomach Mucosa	stomach
50	chr9:97790200-97792000	Enhancers	Brain Inferior Temporal Lobe	brain

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