Variant report

Variant	rs10910945
Chromosome Location	chr1:172004280-172004281
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 38 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:36)

rs_ID	r²[population]
rs10442603	0.94[CHB][hapmap];0.81[ASN][1000 genomes]
rs10797735	1.00[CEU][hapmap];0.93[EUR][1000 genomes]
rs10797736	1.00[CEU][hapmap];0.94[CHB][hapmap];0.90[JPT][hapmap];1.00[YRI][hapmap];0.87[AFR][1000 genomes];0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10910938	0.94[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs10911111	0.80[JPT][hapmap]
rs10911124	0.80[JPT][hapmap]
rs10911125	0.80[JPT][hapmap]
rs12037820	0.86[EUR][1000 genomes]
rs12038713	0.93[EUR][1000 genomes]
rs12117623	0.83[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12119190	1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1475230	0.80[JPT][hapmap]
rs1475231	0.81[JPT][hapmap]
rs2057302	1.00[CEU][hapmap];0.93[EUR][1000 genomes]
rs2057303	0.93[EUR][1000 genomes]
rs2295610	1.00[CEU][hapmap];0.93[EUR][1000 genomes]
rs2295611	1.00[CEU][hapmap];0.93[EUR][1000 genomes]
rs2421987	1.00[CHB][hapmap];0.80[JPT][hapmap]
rs36178280	0.89[EUR][1000 genomes]
rs36180993	0.91[EUR][1000 genomes]
rs4076678	1.00[CEU][hapmap];0.92[EUR][1000 genomes]
rs4333881	0.92[EUR][1000 genomes]
rs4489594	0.93[EUR][1000 genomes]
rs4604727	0.94[CHB][hapmap];0.81[JPT][hapmap];0.82[ASN][1000 genomes]
rs4916413	0.95[EUR][1000 genomes]
rs6413836	0.90[ASN][1000 genomes]
rs6425599	1.00[CEU][hapmap];0.93[EUR][1000 genomes]
rs6425600	0.92[EUR][1000 genomes]
rs6669406	1.00[CEU][hapmap];0.93[EUR][1000 genomes]
rs6700538	0.93[EUR][1000 genomes]
rs72719073	0.87[ASN][1000 genomes]
rs72719075	0.87[ASN][1000 genomes]
rs7518865	1.00[CEU][hapmap];0.93[EUR][1000 genomes]
rs7519823	0.94[CHB][hapmap];0.82[JPT][hapmap];0.82[ASN][1000 genomes]
rs7530970	1.00[CEU][hapmap];0.93[EUR][1000 genomes]
rs7533694	1.00[CEU][hapmap];0.93[EUR][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	nsv532342	chr1:171922237-172133785	Weak transcription Flanking Active TSS Enhancers Strong transcription Transcr. at gene 5' and 3' Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	62 gene(s)	inside rSNPs	diseases
2	nsv3532	chr1:171997451-172042351	Strong transcription Enhancers Weak transcription Genic enhancers Active TSS Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:22 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:171994000-172020400	Weak transcription	Left Ventricle	heart
2	chr1:171994200-172009000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr1:171999000-172006800	Weak transcription	Brain Inferior Temporal Lobe	brain
4	chr1:171999600-172006800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
5	chr1:172000000-172012800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
6	chr1:172000400-172006800	Weak transcription	Brain Hippocampus Middle	brain
7	chr1:172000400-172009800	Weak transcription	Brain Angular Gyrus	brain
8	chr1:172000600-172007000	Weak transcription	Psoas Muscle	Psoas
9	chr1:172000600-172013600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
10	chr1:172000800-172011400	Weak transcription	Right Ventricle	heart
11	chr1:172000800-172013800	Weak transcription	Fetal Brain Female	brain
12	chr1:172001000-172006800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr1:172001400-172019000	Weak transcription	Fetal Brain Male	brain
14	chr1:172001600-172006800	Weak transcription	Brain Substantia Nigra	brain
15	chr1:172002200-172011600	Weak transcription	Brain Cingulate Gyrus	brain
16	chr1:172002800-172013200	Weak transcription	Primary T cells from cord blood	blood
17	chr1:172003000-172012400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
18	chr1:172003200-172006800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
19	chr1:172003200-172008200	Weak transcription	Cortex derived primary cultured neurospheres	brain
20	chr1:172003200-172009800	Weak transcription	Brain Anterior Caudate	brain
21	chr1:172004000-172014000	Weak transcription	Lung	lung
22	chr1:172004200-172008800	Weak transcription	NHEK	skin

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