Variant report

Variant	rs1197304
Chromosome Location	chr3:133104631-133104632
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr3:133100753..133103511-chr3:133104610..133107430,2	K562	blood:
2	chr3:133103700..133105206-chr3:133145260..133147537,2	MCF-7	breast:
3	chr3:133103166..133105237-chr3:133107966..133110867,2	MCF-7	breast:

Extended variants
information (count: 50 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:46)

rs_ID	r²[population]
rs1109858	0.82[JPT][hapmap]
rs1114630	1.00[CHB][hapmap];0.98[CHD][hapmap];0.95[GIH][hapmap];1.00[JPT][hapmap];0.91[MEX][hapmap];0.93[TSI][hapmap];0.90[AMR][1000 genomes];0.84[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1197287	0.95[CHB][hapmap];0.91[JPT][hapmap];0.91[AMR][1000 genomes];0.83[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1197288	0.95[CHB][hapmap];1.00[JPT][hapmap];0.93[AMR][1000 genomes];0.84[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1197293	0.85[CHB][hapmap];0.81[JPT][hapmap];0.84[ASN][1000 genomes]
rs1197296	0.85[CEU][hapmap];1.00[CHB][hapmap];0.93[CHD][hapmap];0.95[GIH][hapmap];1.00[JPT][hapmap];0.85[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs1197297	0.91[CHB][hapmap];0.95[JPT][hapmap];0.94[ASN][1000 genomes]
rs1197298	0.95[CHB][hapmap];0.98[CHD][hapmap];1.00[JPT][hapmap];0.89[LWK][hapmap];0.82[MKK][hapmap];0.83[YRI][hapmap];0.86[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs1197299	1.00[CHB][hapmap];0.98[CHD][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs1197301	0.87[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs1197302	0.92[CEU][hapmap];0.95[CHB][hapmap];0.91[CHD][hapmap];0.84[GIH][hapmap];1.00[JPT][hapmap];0.87[MEX][hapmap];0.88[TSI][hapmap];0.85[AMR][1000 genomes];0.84[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1197305	0.85[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[YRI][hapmap];0.91[AFR][1000 genomes];0.91[AMR][1000 genomes];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1197306	0.95[CHB][hapmap];1.00[JPT][hapmap];0.83[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs1197308	0.82[CHB][hapmap];0.82[JPT][hapmap]
rs1197309	1.00[CEU][hapmap];0.95[CHB][hapmap];0.98[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.98[MKK][hapmap];1.00[TSI][hapmap];0.88[YRI][hapmap];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1197313	1.00[CHB][hapmap];1.00[CHD][hapmap];0.80[GIH][hapmap];1.00[JPT][hapmap];0.83[MEX][hapmap];0.80[TSI][hapmap];0.89[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs1197314	0.91[CHB][hapmap];0.98[CHD][hapmap];1.00[JPT][hapmap];0.80[MEX][hapmap];0.96[ASN][1000 genomes]
rs1201671	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.90[AMR][1000 genomes];0.89[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1201673	0.91[CHB][hapmap];0.93[CHD][hapmap];0.95[JPT][hapmap];0.93[ASN][1000 genomes]
rs12631678	0.91[CHB][hapmap];0.95[JPT][hapmap];0.92[ASN][1000 genomes]
rs1619552	0.85[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.83[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs1619622	0.85[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.83[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs1708376	0.87[AMR][1000 genomes];0.84[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1708377	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.91[AMR][1000 genomes];0.89[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1708384	0.83[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs1708385	0.87[CHB][hapmap];0.93[CHD][hapmap];0.95[JPT][hapmap];0.94[ASN][1000 genomes]
rs1795101	0.82[JPT][hapmap]
rs1795104	0.94[ASN][1000 genomes]
rs1795107	0.85[CEU][hapmap];0.95[CHB][hapmap];0.98[CHD][hapmap];0.95[GIH][hapmap];1.00[JPT][hapmap];0.80[MEX][hapmap];0.80[TSI][hapmap];0.88[AMR][1000 genomes];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2089987	0.83[CHB][hapmap];0.95[JPT][hapmap];0.90[ASN][1000 genomes]
rs2670179	1.00[CEU][hapmap];0.95[CHB][hapmap];0.91[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.91[MEX][hapmap];0.93[TSI][hapmap];0.93[AMR][1000 genomes];0.89[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2699880	0.83[CHB][hapmap];0.86[CHD][hapmap];0.95[JPT][hapmap];0.88[ASN][1000 genomes]
rs2699882	1.00[CEU][hapmap];0.95[CHB][hapmap];0.91[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.86[MEX][hapmap];0.93[TSI][hapmap];0.90[AMR][1000 genomes];0.89[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs3732572	0.87[CHB][hapmap];0.86[CHD][hapmap];0.95[JPT][hapmap];0.92[ASN][1000 genomes]
rs4854583	0.90[ASN][1000 genomes]
rs4854719	1.00[CHB][hapmap];0.98[CHD][hapmap];0.95[JPT][hapmap];0.81[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs4854720	0.83[CHB][hapmap];0.95[JPT][hapmap];0.90[ASN][1000 genomes]
rs56181416	0.81[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs656721	0.89[CEU][hapmap];0.95[JPT][hapmap];0.85[TSI][hapmap]
rs6780144	0.91[ASN][1000 genomes]
rs6802663	0.87[CHB][hapmap];0.95[JPT][hapmap];0.87[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs938230	0.84[CHD][hapmap]
rs938231	0.86[ASN][1000 genomes]
rs9850193	0.82[CHB][hapmap];0.89[CHD][hapmap];0.95[JPT][hapmap];0.90[ASN][1000 genomes]
rs9853752	0.95[ASN][1000 genomes]
rs9853757	0.95[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	nsv877503	chr3:133035774-133104631	Bivalent/Poised TSS Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
2	nsv460857	chr3:133101390-133122216	Strong transcription Enhancers Weak transcription Genic enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	nsv591801	chr3:133101390-133122216	Weak transcription Enhancers ZNF genes & repeats Strong transcription Genic enhancers Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	esv3360224	chr3:133103962-133107460	Weak transcription Enhancers Bivalent Enhancer Strong transcription	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:33 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:133094000-133109000	Weak transcription	HSMM	muscle
2	chr3:133094800-133110400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr3:133096000-133107800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr3:133099000-133117000	Weak transcription	Placenta	Placenta
5	chr3:133099600-133122600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
6	chr3:133100800-133111600	Weak transcription	HSMMtube	muscle
7	chr3:133102400-133112400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
8	chr3:133103400-133109000	Weak transcription	Fetal Stomach	stomach
9	chr3:133103400-133111600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr3:133103400-133112400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
11	chr3:133103400-133115200	Weak transcription	Lung	lung
12	chr3:133103400-133123200	Weak transcription	H1 Cell Line	embryonic stem cell
13	chr3:133103400-133123600	Weak transcription	H9 Cell Line	embryonic stem cell
14	chr3:133103800-133105800	Weak transcription	Cortex derived primary cultured neurospheres	brain
15	chr3:133103800-133106400	Weak transcription	Fetal Thymus	thymus
16	chr3:133103800-133107800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
17	chr3:133103800-133108600	Weak transcription	Fetal Lung	lung
18	chr3:133103800-133109000	Weak transcription	Brain Hippocampus Middle	brain
19	chr3:133103800-133109200	Weak transcription	Brain Angular Gyrus	brain
20	chr3:133103800-133109200	Weak transcription	Skeletal Muscle Male	skeletal muscle
21	chr3:133103800-133109400	Weak transcription	Fetal Brain Male	brain
22	chr3:133103800-133109600	Weak transcription	Skeletal Muscle Female	skeletal muscle
23	chr3:133103800-133109800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
24	chr3:133103800-133112000	Weak transcription	Brain Cingulate Gyrus	brain
25	chr3:133103800-133115800	Weak transcription	Fetal Muscle Leg	muscle
26	chr3:133103800-133118600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
27	chr3:133103800-133123800	Weak transcription	Brain Anterior Caudate	brain
28	chr3:133104000-133105600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
29	chr3:133104000-133112000	Weak transcription	Brain Inferior Temporal Lobe	brain
30	chr3:133104000-133122200	Weak transcription	Brain Substantia Nigra	brain
31	chr3:133104200-133109000	Weak transcription	Brain Germinal Matrix	brain
32	chr3:133104400-133112000	Strong transcription	Fetal Brain Female	brain
33	chr3:133104400-133131400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell

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