Variant report

Variant	rs12110370
Chromosome Location	chr6:118455669-118455670
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 43 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:39)

rs_ID	r²[population]
rs10484290	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.89[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.92[LWK][hapmap];1.00[MEX][hapmap];0.98[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10499085	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs11153722	1.00[CEU][hapmap];1.00[CHB][hapmap]
rs11153724	1.00[CEU][hapmap];1.00[CHB][hapmap];0.93[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs11754233	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs11754931	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs11755798	0.85[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11759870	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs11962053	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11962518	0.85[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs11963467	1.00[CEU][hapmap];1.00[CHB][hapmap];0.83[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.86[MKK][hapmap];1.00[TSI][hapmap]
rs11965805	0.87[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs1334831	0.85[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs1334832	0.87[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs1334833	0.88[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs1334834	1.00[CEU][hapmap];1.00[CHB][hapmap];0.83[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.86[MKK][hapmap];1.00[TSI][hapmap];0.88[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs1334836	0.86[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs1334838	0.86[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs1334839	1.00[CEU][hapmap];1.00[CHB][hapmap];0.83[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.97[TSI][hapmap]
rs1334840	1.00[CEU][hapmap];1.00[CHB][hapmap];0.83[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.86[MKK][hapmap];1.00[TSI][hapmap]
rs17334660	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17822466	0.86[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs2883773	1.00[CEU][hapmap];1.00[CHB][hapmap];0.83[GIH][hapmap];1.00[JPT][hapmap];0.88[MEX][hapmap];0.97[TSI][hapmap];0.85[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs3923321	0.85[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs3923322	1.00[CEU][hapmap];0.83[GIH][hapmap];0.94[MEX][hapmap];0.97[TSI][hapmap];0.85[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs4028067	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4479972	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.86[MKK][hapmap];1.00[TSI][hapmap];0.88[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs4512262	1.00[CEU][hapmap];1.00[CHB][hapmap];0.83[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.86[MKK][hapmap];0.97[TSI][hapmap]
rs4593395	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs6909791	1.00[JPT][hapmap]
rs6940758	1.00[CEU][hapmap];0.83[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.97[TSI][hapmap];0.88[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs72961889	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs756290	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs7740975	1.00[JPT][hapmap]
rs7743666	1.00[CEU][hapmap];1.00[CHB][hapmap];0.83[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.86[MKK][hapmap];1.00[TSI][hapmap]
rs7743889	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs7743917	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs7775284	1.00[CEU][hapmap];0.85[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs977793	1.00[CEU][hapmap];0.83[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.97[TSI][hapmap];0.88[AMR][1000 genomes];0.99[EUR][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	nsv530526	chr6:118027339-118718476	Weak transcription Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
2	nsv428153	chr6:118430517-118586974	Weak transcription Enhancers Strong transcription Active TSS ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
3	nsv1030089	chr6:118436482-118604516	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	nsv538427	chr6:118436482-118604516	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Genic enhancers	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs12110370	SLC35F1	cis	parietal	SCAN

Chromatin state (count:20 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:118453400-118456800	Enhancers	Fetal Lung	lung
2	chr6:118454000-118457200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
3	chr6:118454000-118457400	Enhancers	Fetal Stomach	stomach
4	chr6:118454000-118460200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
5	chr6:118454200-118457200	Enhancers	Cortex derived primary cultured neurospheres	brain
6	chr6:118455000-118455800	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
7	chr6:118455000-118455800	Enhancers	Right Atrium	heart
8	chr6:118455000-118456000	Enhancers	Left Ventricle	heart
9	chr6:118455000-118456400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr6:118455000-118456400	Enhancers	Fetal Kidney	kidney
11	chr6:118455200-118455800	Enhancers	Stomach Smooth Muscle	stomach
12	chr6:118455200-118456200	Enhancers	Brain Cingulate Gyrus	brain
13	chr6:118455200-118457200	Enhancers	Brain Germinal Matrix	brain
14	chr6:118455400-118456200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr6:118455400-118456400	Enhancers	Brain Anterior Caudate	brain
16	chr6:118455600-118456000	Enhancers	Skeletal Muscle Female	skeletal muscle
17	chr6:118455600-118456000	Enhancers	Spleen	Spleen
18	chr6:118455600-118456400	Enhancers	Brain Hippocampus Middle	brain
19	chr6:118455600-118456800	Enhancers	Fetal Muscle Leg	muscle
20	chr6:118455600-118457000	Enhancers	Fetal Brain Male	brain

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