Variant report

Variant	rs9803815
Chromosome Location	chr1:62741198-62741199
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 36 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:32)

rs_ID	r²[population]
rs10157938	0.88[JPT][hapmap]
rs10465842	0.90[JPT][hapmap]
rs10493318	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.82[LWK][hapmap];0.95[MEX][hapmap];0.96[MKK][hapmap];1.00[TSI][hapmap];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10889318	0.90[JPT][hapmap]
rs11207955	0.94[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.98[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];0.93[YRI][hapmap];0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11207956	0.83[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12031172	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12031176	1.00[CEU][hapmap];0.88[CHB][hapmap];1.00[JPT][hapmap];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12038843	0.81[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.84[ASN][1000 genomes]
rs12043263	0.85[AFR][1000 genomes];0.87[AMR][1000 genomes];0.86[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12123763	0.85[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12127630	0.92[CEU][hapmap];0.90[CHB][hapmap];0.92[CHD][hapmap];0.90[JPT][hapmap];0.85[MKK][hapmap];0.91[TSI][hapmap];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12138544	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs17855078	0.87[ASN][1000 genomes]
rs1886834	0.90[JPT][hapmap]
rs1925827	0.81[CEU][hapmap];0.86[JPT][hapmap]
rs2666509	0.90[JPT][hapmap]
rs2765266	0.90[JPT][hapmap]
rs2765268	0.90[JPT][hapmap]
rs2765269	0.90[JPT][hapmap]
rs34477066	0.87[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs3850629	0.88[CHB][hapmap];1.00[JPT][hapmap]
rs3850632	0.84[CEU][hapmap];0.83[EUR][1000 genomes]
rs3861936	0.81[CHB][hapmap];1.00[JPT][hapmap]
rs4915606	0.90[JPT][hapmap]
rs4915607	0.90[JPT][hapmap]
rs6675508	0.90[JPT][hapmap]
rs6680736	0.81[CEU][hapmap]
rs6691591	0.81[CEU][hapmap]
rs881548	0.90[JPT][hapmap]
rs9803854	0.80[EUR][1000 genomes]
rs9804022	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes];0.97[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	nsv1004446	chr1:62394631-62813533	Enhancers ZNF genes & repeats Weak transcription Bivalent/Poised TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	12 gene(s)	inside rSNPs	diseases
2	nsv534984	chr1:62394631-62813533	Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Strong transcription ZNF genes & repeats Bivalent/Poised TSS Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	12 gene(s)	inside rSNPs	diseases
3	nsv1009398	chr1:62656660-62780644	Flanking Active TSS Enhancers Active TSS Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	nsv1013582	chr1:62723703-62910632	Flanking Active TSS Enhancers Weak transcription Strong transcription Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	31 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:25 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:62732400-62748400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr1:62734200-62750800	Weak transcription	Gastric	stomach
3	chr1:62737600-62741800	Strong transcription	Placenta	Placenta
4	chr1:62737800-62742600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr1:62737800-62744400	Weak transcription	Fetal Intestine Large	intestine
6	chr1:62738000-62749000	Weak transcription	H9 Cell Line	embryonic stem cell
7	chr1:62738200-62746400	Weak transcription	Fetal Kidney	kidney
8	chr1:62738200-62751200	Weak transcription	Rectal Mucosa Donor 29	rectum
9	chr1:62739600-62744200	Weak transcription	Primary T helper cells PMA-I stimulated	--
10	chr1:62740000-62741200	Enhancers	Fetal Heart	heart
11	chr1:62740200-62746400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
12	chr1:62740400-62743200	Weak transcription	Liver	Liver
13	chr1:62740400-62744600	Weak transcription	Fetal Thymus	thymus
14	chr1:62740400-62745400	Weak transcription	Fetal Lung	lung
15	chr1:62740400-62746600	Weak transcription	Pancreas	Pancrea
16	chr1:62740600-62741800	Enhancers	Fetal Muscle Leg	muscle
17	chr1:62740600-62743000	Weak transcription	Fetal Intestine Small	intestine
18	chr1:62740600-62744400	Weak transcription	Placenta Amnion	Placenta Amnion
19	chr1:62740600-62744600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
20	chr1:62740600-62744600	Weak transcription	Fetal Muscle Trunk	muscle
21	chr1:62740800-62741200	Enhancers	Fetal Stomach	stomach
22	chr1:62740800-62741400	Enhancers	Adipose Nuclei	Adipose
23	chr1:62740800-62742800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
24	chr1:62741000-62741400	Enhancers	Brain Germinal Matrix	brain
25	chr1:62741000-62745000	Weak transcription	HepG2	liver

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