Variant report

Variant	rs10194333
Chromosome Location	chr2:210715307-210715308
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 81 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:79)

rs_ID	r²[population]
rs10178425	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10178431	0.85[YRI][hapmap];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10178675	0.96[YRI][hapmap];0.84[AFR][1000 genomes];0.81[AMR][1000 genomes];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10188289	0.92[YRI][hapmap];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10189597	0.88[AFR][1000 genomes];0.81[EUR][1000 genomes]
rs10194322	1.00[CEU][hapmap];0.88[YRI][hapmap];0.88[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10490024	0.86[YRI][hapmap];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10490025	1.00[CEU][hapmap]
rs10490026	1.00[CEU][hapmap]
rs10490027	1.00[CEU][hapmap]
rs11270377	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1160565	0.88[AFR][1000 genomes];0.83[EUR][1000 genomes]
rs11682914	1.00[CEU][hapmap]
rs11688226	1.00[CEU][hapmap]
rs11691952	0.83[EUR][1000 genomes]
rs11694132	1.00[CEU][hapmap]
rs11695433	0.83[EUR][1000 genomes]
rs12328328	1.00[CEU][hapmap]
rs12328346	1.00[CEU][hapmap]
rs12328869	1.00[CEU][hapmap]
rs12328884	1.00[CEU][hapmap]
rs12329111	1.00[CEU][hapmap]
rs12329303	1.00[CEU][hapmap]
rs12386218	0.86[YRI][hapmap];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12993178	0.81[EUR][1000 genomes]
rs13010861	0.81[EUR][1000 genomes]
rs13010864	0.83[EUR][1000 genomes]
rs13013030	1.00[CEU][hapmap];0.83[EUR][1000 genomes]
rs13028068	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13398209	0.85[AFR][1000 genomes];0.81[EUR][1000 genomes]
rs13398411	0.88[AFR][1000 genomes];0.81[EUR][1000 genomes]
rs13414802	0.83[YRI][hapmap]
rs1558474	1.00[CEU][hapmap]
rs16843780	0.96[YRI][hapmap];0.84[AFR][1000 genomes];0.81[AMR][1000 genomes];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16843821	0.82[EUR][1000 genomes]
rs16843893	1.00[CEU][hapmap]
rs17748674	1.00[CEU][hapmap]
rs17748692	1.00[CEU][hapmap]
rs17748818	1.00[CEU][hapmap]
rs2109970	1.00[CEU][hapmap]
rs2159746	0.88[AFR][1000 genomes];0.83[EUR][1000 genomes]
rs2159747	1.00[CEU][hapmap];0.83[EUR][1000 genomes]
rs2191906	0.96[YRI][hapmap];0.81[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs2191908	0.83[EUR][1000 genomes]
rs2191909	1.00[CEU][hapmap];0.89[YRI][hapmap];0.88[AFR][1000 genomes];0.83[EUR][1000 genomes]
rs34038887	0.81[EUR][1000 genomes]
rs34073663	0.81[EUR][1000 genomes]
rs34115158	0.83[EUR][1000 genomes]
rs34395024	0.88[AFR][1000 genomes];0.83[EUR][1000 genomes]
rs34434902	0.81[EUR][1000 genomes]
rs34920752	0.83[EUR][1000 genomes]
rs35969300	0.83[EUR][1000 genomes]
rs6712943	0.81[EUR][1000 genomes]
rs6729513	0.83[EUR][1000 genomes]
rs6739769	1.00[CEU][hapmap]
rs6752217	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6757148	0.88[AFR][1000 genomes];0.83[EUR][1000 genomes]
rs7566741	1.00[CEU][hapmap]
rs7567142	0.83[AFR][1000 genomes]
rs7579121	1.00[CEU][hapmap];0.83[EUR][1000 genomes]
rs7581628	1.00[CEU][hapmap]
rs7581974	1.00[CEU][hapmap]
rs7583147	0.88[AFR][1000 genomes];0.81[EUR][1000 genomes]
rs7584039	1.00[CEU][hapmap];0.82[EUR][1000 genomes]
rs7593426	1.00[CEU][hapmap]
rs7594368	0.83[EUR][1000 genomes]
rs7595063	1.00[CEU][hapmap];0.84[YRI][hapmap];0.86[AFR][1000 genomes];0.81[EUR][1000 genomes]
rs7598071	1.00[CEU][hapmap];0.85[YRI][hapmap];0.88[AFR][1000 genomes];0.81[EUR][1000 genomes]
rs9288414	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9630977	0.88[AFR][1000 genomes];0.81[EUR][1000 genomes]
rs9631001	1.00[CEU][hapmap];0.89[YRI][hapmap];0.88[AFR][1000 genomes];0.81[EUR][1000 genomes]
rs9677274	0.81[EUR][1000 genomes]
rs9677282	0.81[EUR][1000 genomes]
rs9973317	1.00[CEU][hapmap];0.88[YRI][hapmap];0.88[AFR][1000 genomes];0.81[EUR][1000 genomes]
rs9973465	0.88[AFR][1000 genomes]
rs9973473	0.88[AFR][1000 genomes];0.81[EUR][1000 genomes]
rs9973633	0.81[EUR][1000 genomes]
rs9973787	1.00[CEU][hapmap];0.87[YRI][hapmap];0.88[AFR][1000 genomes];0.81[EUR][1000 genomes]
rs9973848	1.00[CEU][hapmap];0.88[YRI][hapmap];0.88[AFR][1000 genomes];0.81[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	nsv431969	chr2:210682494-211074494	Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
2	nsv1004426	chr2:210709999-211001680	Strong transcription Weak transcription Enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:210682000-210769600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
2	chr2:210686000-210720400	Weak transcription	Brain Angular Gyrus	brain
3	chr2:210705200-210718000	Weak transcription	Brain Inferior Temporal Lobe	brain
4	chr2:210705400-210715600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
5	chr2:210705600-210720200	Weak transcription	Cortex derived primary cultured neurospheres	brain
6	chr2:210706000-210715800	Weak transcription	Fetal Brain Female	brain
7	chr2:210706000-210719200	Weak transcription	Brain Anterior Caudate	brain
8	chr2:210707800-210718800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain

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