Variant report

Variant	rs4499618
Chromosome Location	chr3:85081211-85081212
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 42 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs1016305	0.90[CHB][hapmap];0.82[JPT][hapmap]
rs1016306	0.91[CHB][hapmap];0.83[JPT][hapmap]
rs11927760	0.80[ASN][1000 genomes]
rs1248858	0.90[CHB][hapmap];0.86[JPT][hapmap];0.84[ASN][1000 genomes]
rs1248859	0.85[CHB][hapmap];0.87[JPT][hapmap];0.84[ASN][1000 genomes]
rs1248860	0.81[CHB][hapmap]
rs13072305	0.94[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs13081745	0.90[CHB][hapmap];0.87[JPT][hapmap];0.86[ASN][1000 genomes]
rs1694977	0.86[CHB][hapmap];0.87[JPT][hapmap];0.85[ASN][1000 genomes]
rs1872553	0.81[CHB][hapmap]
rs1872556	0.91[CHB][hapmap];0.87[JPT][hapmap];0.86[ASN][1000 genomes]
rs1994315	0.84[CEU][hapmap];0.89[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs2035561	0.90[CHB][hapmap];0.87[JPT][hapmap];0.85[ASN][1000 genomes]
rs2035562	0.86[CHB][hapmap];0.85[ASN][1000 genomes]
rs2062431	0.95[CEU][hapmap];0.94[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs2087011	0.81[JPT][hapmap];0.80[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2200461	0.94[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs2220243	0.90[CEU][hapmap];0.90[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs2326123	0.91[CHB][hapmap];0.87[JPT][hapmap];0.86[ASN][1000 genomes]
rs2326126	0.94[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs4301023	0.85[CHB][hapmap]
rs4569672	0.85[ASN][1000 genomes]
rs4856559	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.88[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4856560	0.95[CEU][hapmap];0.96[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs56808719	0.80[ASN][1000 genomes]
rs6549009	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6768559	0.94[CEU][hapmap];0.94[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs6801271	0.82[CHB][hapmap];0.80[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7645952	0.95[CEU][hapmap];0.93[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs7647649	0.84[CEU][hapmap];0.88[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs7651996	0.85[CHB][hapmap]
rs765461	1.00[CEU][hapmap];0.95[CHB][hapmap];0.91[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.92[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9814390	0.85[CEU][hapmap];0.92[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs9831123	0.81[CHB][hapmap]
rs9855054	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs9869902	0.95[CEU][hapmap];0.94[AMR][1000 genomes];0.93[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1002058	chr3:84757044-85389876	Bivalent Enhancer Enhancers Active TSS Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	esv1829788	chr3:84926769-85086403	Enhancers Bivalent Enhancer Active TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
3	esv3419993	chr3:85030343-85663403	Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region miRNA	2 gene(s)	inside rSNPs	diseases
4	nsv492289	chr3:85066623-85319147	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Strong transcription	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
5	esv2753915	chr3:85071410-85624810	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region miRNA	2 gene(s)	inside rSNPs	diseases
6	esv3445418	chr3:85081096-85081304	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:17 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:85055800-85081400	Weak transcription	Cortex derived primary cultured neurospheres	brain
2	chr3:85065200-85082200	Weak transcription	Brain Hippocampus Middle	brain
3	chr3:85068600-85090600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
4	chr3:85071400-85082400	Weak transcription	Fetal Brain Female	brain
5	chr3:85071600-85082000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
6	chr3:85071800-85081400	Weak transcription	Brain Angular Gyrus	brain
7	chr3:85078800-85081800	Weak transcription	Brain Inferior Temporal Lobe	brain
8	chr3:85079600-85083200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
9	chr3:85079600-85083600	Weak transcription	HUES6 Cell Line	embryonic stem cell
10	chr3:85079600-85086400	Weak transcription	H9 Cell Line	embryonic stem cell
11	chr3:85079800-85082200	Weak transcription	Psoas Muscle	Psoas
12	chr3:85080000-85082200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
13	chr3:85080000-85082800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
14	chr3:85080000-85083400	Weak transcription	HUES64 Cell Line	embryonic stem cell
15	chr3:85080400-85082400	Weak transcription	H1 Cell Line	embryonic stem cell
16	chr3:85080400-85082800	Weak transcription	HUES48 Cell Line	embryonic stem cell
17	chr3:85081200-85081400	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain

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