Variant report

Variant	rs4735574
Chromosome Location	chr8:99737278-99737279
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr8:99736975..99738718-chr8:99836391..99838419,2	MCF-7	breast:
2	chr8:99735526..99738976-chr8:99742014..99743636,3	K562	blood:

Variant related genes	Relation type
ENSG00000104375	Chromatin interaction

Extended variants
information (count: 105 )
Associated
traits (count: 3 )

rSNPs within LD-proxies of this variant (count:98)

rs_ID	r²[population]
rs10447977	0.86[JPT][hapmap];0.95[MEX][hapmap];0.95[TSI][hapmap];0.82[YRI][hapmap];0.88[AMR][1000 genomes]
rs10755896	0.82[CHB][hapmap];0.98[CHD][hapmap];0.95[MEX][hapmap];0.95[TSI][hapmap];0.82[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs10755897	0.81[CHB][hapmap];0.95[CHD][hapmap];0.89[LWK][hapmap];0.95[MEX][hapmap];0.90[TSI][hapmap];0.82[YRI][hapmap];0.82[AMR][1000 genomes]
rs10955186	0.86[GIH][hapmap];0.95[MEX][hapmap];0.88[TSI][hapmap]
rs10955187	0.86[GIH][hapmap];0.95[MEX][hapmap];0.88[TSI][hapmap]
rs10955189	0.91[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs10955190	0.86[CEU][hapmap];0.87[CHB][hapmap];0.91[JPT][hapmap];0.97[AMR][1000 genomes];0.89[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11774463	0.82[CHB][hapmap];0.98[CHD][hapmap];0.91[JPT][hapmap];0.95[MEX][hapmap];0.95[TSI][hapmap];0.94[AMR][1000 genomes];0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs11778767	0.83[CHD][hapmap];0.96[GIH][hapmap];0.91[JPT][hapmap];0.87[MEX][hapmap];0.97[TSI][hapmap];0.82[YRI][hapmap];0.87[AMR][1000 genomes]
rs11780292	0.86[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs11780369	0.86[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs11780500	0.84[CHD][hapmap];0.96[GIH][hapmap];0.91[JPT][hapmap];0.87[MEX][hapmap];0.95[TSI][hapmap];0.82[YRI][hapmap];0.87[AMR][1000 genomes]
rs11785245	0.81[JPT][hapmap]
rs12114834	0.96[GIH][hapmap];0.86[JPT][hapmap];0.87[MEX][hapmap];0.97[TSI][hapmap];0.82[YRI][hapmap];0.87[AMR][1000 genomes]
rs12541317	0.84[AMR][1000 genomes]
rs12542069	0.91[MEX][hapmap];0.83[TSI][hapmap]
rs12542649	0.82[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs12542758	0.83[LWK][hapmap];0.91[MEX][hapmap];0.83[TSI][hapmap];0.82[YRI][hapmap]
rs12547297	0.82[CHB][hapmap];0.98[CHD][hapmap];0.91[JPT][hapmap];0.95[MEX][hapmap];0.90[TSI][hapmap];0.92[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs12549803	0.98[CHD][hapmap];0.81[JPT][hapmap];0.87[MEX][hapmap];0.90[TSI][hapmap];0.86[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs12550012	0.88[CHD][hapmap]
rs12550783	0.82[CHB][hapmap];0.93[CHD][hapmap];0.95[MEX][hapmap];0.90[TSI][hapmap];0.80[AMR][1000 genomes]
rs12675964	0.86[CHD][hapmap]
rs12677183	0.86[CEU][hapmap];0.87[CHB][hapmap];0.98[CHD][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];0.95[TSI][hapmap]
rs12679268	0.81[AFR][1000 genomes];0.81[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs12679734	0.95[MEX][hapmap];0.90[TSI][hapmap];0.86[AMR][1000 genomes]
rs12680195	0.81[CHB][hapmap];0.95[CHD][hapmap];0.91[JPT][hapmap];0.89[LWK][hapmap];0.95[MEX][hapmap];0.87[TSI][hapmap];0.82[YRI][hapmap];0.81[AFR][1000 genomes];0.92[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs12680602	0.81[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs13257475	0.83[CHB][hapmap]
rs13269932	1.00[CEU][hapmap];0.87[CHB][hapmap];0.98[CHD][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.97[AMR][1000 genomes];0.93[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs13271844	0.82[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs13275915	1.00[CEU][hapmap];0.87[CHB][hapmap];0.98[CHD][hapmap];1.00[GIH][hapmap];0.91[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs13279438	0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1447245	0.91[MEX][hapmap]
rs1476181	0.82[YRI][hapmap];0.88[AMR][1000 genomes]
rs16897076	0.83[CHB][hapmap];0.89[CHD][hapmap]
rs1961744	0.80[AMR][1000 genomes]
rs2442012	0.90[AMR][1000 genomes]
rs2442014	0.90[AMR][1000 genomes]
rs2515214	0.96[GIH][hapmap];1.00[MEX][hapmap];0.93[TSI][hapmap];0.82[YRI][hapmap];0.89[AMR][1000 genomes]
rs2515216	0.96[GIH][hapmap];0.95[TSI][hapmap]
rs2922066	0.95[MEX][hapmap];0.85[TSI][hapmap]
rs2922073	0.80[AMR][1000 genomes]
rs2922074	0.80[AMR][1000 genomes]
rs2922075	0.85[AMR][1000 genomes]
rs2922076	0.80[AMR][1000 genomes]
rs2922078	0.92[GIH][hapmap];1.00[MEX][hapmap];0.90[TSI][hapmap];0.85[AMR][1000 genomes]
rs2922081	0.85[AMR][1000 genomes]
rs2922082	0.92[GIH][hapmap];1.00[MEX][hapmap];0.90[TSI][hapmap];0.81[AMR][1000 genomes]
rs3019293	0.85[AMR][1000 genomes]
rs34114299	0.82[CHB][hapmap];0.98[CHD][hapmap];0.95[MEX][hapmap];0.95[TSI][hapmap]
rs34281206	0.88[AMR][1000 genomes]
rs34366206	0.86[JPT][hapmap];0.82[MEX][hapmap];0.92[TSI][hapmap];0.81[AMR][1000 genomes]
rs34477118	0.88[AMR][1000 genomes]
rs34855977	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs35536167	0.88[AMR][1000 genomes]
rs35798019	0.81[CHD][hapmap];0.96[GIH][hapmap];0.91[JPT][hapmap];0.87[MEX][hapmap];0.90[TSI][hapmap];0.84[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs35804297	0.81[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs4131873	0.82[ASW][hapmap];0.86[CEU][hapmap];0.87[CHB][hapmap];0.98[CHD][hapmap];0.86[GIH][hapmap];0.91[JPT][hapmap];0.94[LWK][hapmap];1.00[MEX][hapmap];0.90[MKK][hapmap];0.95[TSI][hapmap];1.00[YRI][hapmap];0.92[AFR][1000 genomes];0.98[AMR][1000 genomes];0.90[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4255105	0.95[MEX][hapmap];0.90[TSI][hapmap];0.82[YRI][hapmap];0.86[AMR][1000 genomes]
rs4279561	1.00[CEU][hapmap];0.87[CHB][hapmap];0.95[CHD][hapmap];0.83[GIH][hapmap];0.91[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4292660	0.89[GIH][hapmap];0.87[MEX][hapmap];0.84[TSI][hapmap]
rs4304299	0.90[AMR][1000 genomes]
rs4413739	0.89[AMR][1000 genomes]
rs4440607	0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4442112	0.85[GIH][hapmap]
rs4509292	0.82[CHB][hapmap];0.80[AMR][1000 genomes]
rs4517094	0.86[CEU][hapmap];0.87[CHB][hapmap];0.91[AMR][1000 genomes];0.85[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4541872	0.94[AFR][1000 genomes];0.95[AMR][1000 genomes];0.89[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4549741	1.00[CEU][hapmap];0.87[CHB][hapmap];0.95[CHD][hapmap];0.86[GIH][hapmap];0.91[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4562286	0.96[GIH][hapmap];1.00[MEX][hapmap];0.93[TSI][hapmap];0.89[AMR][1000 genomes]
rs4612309	0.96[AFR][1000 genomes];0.98[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs4734410	0.86[CEU][hapmap];0.87[CHB][hapmap];0.98[CHD][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];0.95[TSI][hapmap];0.88[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs4735568	0.91[MEX][hapmap];0.90[TSI][hapmap]
rs4735569	0.86[CHB][hapmap]
rs4735570	0.85[CHD][hapmap];0.84[TSI][hapmap];0.86[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs4735571	0.90[AMR][1000 genomes];0.85[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs57034072	0.92[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs58321500	0.86[AMR][1000 genomes]
rs58679407	0.82[AMR][1000 genomes]
rs62532565	0.96[AFR][1000 genomes];0.97[AMR][1000 genomes];0.93[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs62532577	0.94[AMR][1000 genomes];0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs62532587	0.93[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs62535381	0.81[AMR][1000 genomes]
rs62535382	0.82[AMR][1000 genomes]
rs62535383	0.80[AMR][1000 genomes]
rs62535404	0.80[AMR][1000 genomes]
rs62535408	0.84[AMR][1000 genomes]
rs62535410	0.90[AMR][1000 genomes]
rs62535412	0.92[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs6651182	0.82[CHB][hapmap];0.98[CHD][hapmap];0.95[MEX][hapmap];0.95[TSI][hapmap]
rs6988087	0.93[GIH][hapmap];0.91[JPT][hapmap];0.83[MEX][hapmap];0.86[TSI][hapmap]
rs6992925	1.00[CEU][hapmap];0.87[CHB][hapmap];0.97[CHD][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.83[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs7818010	0.86[CEU][hapmap]
rs7818828	0.87[MEX][hapmap];0.90[TSI][hapmap];0.80[AMR][1000 genomes]
rs7838239	0.91[JPT][hapmap];0.82[YRI][hapmap];0.87[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs7845271	0.89[GIH][hapmap];0.87[MEX][hapmap];0.81[TSI][hapmap]
rs9656842	0.90[TSI][hapmap]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv891218	chr8:99507313-99906221	Weak transcription Flanking Active TSS Enhancers Strong transcription ZNF genes & repeats Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
2	nsv1027025	chr8:99672977-100115315	Weak transcription Bivalent/Poised TSS Bivalent Enhancer Active TSS Enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
3	nsv539690	chr8:99672977-100115315	Weak transcription Flanking Active TSS ZNF genes & repeats Enhancers Strong transcription Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
4	nsv891220	chr8:99681858-99867419	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	7 gene(s)	inside rSNPs	diseases
5	nsv1025685	chr8:99706280-99826236	Strong transcription ZNF genes & repeats Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
6	nsv539691	chr8:99706280-99826236	Weak transcription Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
7	nsv1031089	chr8:99715785-100399935	Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Active TSS Enhancers Strong transcription Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases

mRNA abundance (count:3)

SNP	Gene	Cis/trans	Tissue	Source
rs4735574	NCALD	cis	cerebellum	SCAN
rs4735574	OSR2	cis	cerebellum	SCAN
rs4735574	TMEM14C	trans	cerebellum	SCAN

Chromatin state (count:34 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:99676200-99738200	Weak transcription	Fetal Kidney	kidney
2	chr8:99683600-99738000	Weak transcription	NHEK	skin
3	chr8:99713200-99737600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr8:99723000-99738000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
5	chr8:99723200-99738000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
6	chr8:99723200-99738000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
7	chr8:99723200-99738200	Weak transcription	Lung	lung
8	chr8:99727400-99737400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr8:99728200-99757200	Weak transcription	Primary hematopoietic stem cells	blood
10	chr8:99729200-99738000	Weak transcription	Primary monocytes fromperipheralblood	blood
11	chr8:99731400-99738000	Weak transcription	Psoas Muscle	Psoas
12	chr8:99733000-99738200	Enhancers	Liver	Liver
13	chr8:99734600-99738000	Weak transcription	Adipose Nuclei	Adipose
14	chr8:99735000-99737400	Weak transcription	A549	lung
15	chr8:99735000-99737800	Weak transcription	HepG2	liver
16	chr8:99735200-99738200	Weak transcription	Small Intestine	intestine
17	chr8:99735400-99738000	Weak transcription	Rectal Mucosa Donor 31	rectum
18	chr8:99735600-99738000	Weak transcription	Skeletal Muscle Female	skeletal muscle
19	chr8:99736200-99738000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
20	chr8:99736200-99738200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
21	chr8:99736400-99738000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
22	chr8:99736400-99738000	Enhancers	GM12878-XiMat	blood
23	chr8:99736400-99739200	Enhancers	Primary hematopoietic stem cells short term culture	blood
24	chr8:99736400-99739400	Weak transcription	NHDF-Ad	bronchial
25	chr8:99736600-99737800	Weak transcription	HMEC	breast
26	chr8:99736600-99738000	Weak transcription	Skeletal Muscle Male	skeletal muscle
27	chr8:99736600-99738800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
28	chr8:99736600-99746400	Weak transcription	K562	blood
29	chr8:99737000-99738000	Enhancers	Hela-S3	cervix
30	chr8:99737000-99739200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
31	chr8:99737000-99740000	Enhancers	Breast Myoepithelial Primary Cells	Breast
32	chr8:99737200-99738400	Enhancers	Primary neutrophils fromperipheralblood	blood
33	chr8:99737200-99738400	Enhancers	Monocytes-CD14+_RO01746	blood
34	chr8:99737200-99739000	Enhancers	iPS-15b Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links