Variant report

Variant	rs10225427
Chromosome Location	chr7:150371715-150371716
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 28 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:18)

rs_ID	r²[population]
rs10232092	0.88[ASN][1000 genomes]
rs10244273	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10952285	0.82[EUR][1000 genomes]
rs12703095	0.86[ASN][1000 genomes]
rs16884586	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1949696	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2075078	0.87[EUR][1000 genomes]
rs2110000	0.83[EUR][1000 genomes]
rs2159843	0.83[EUR][1000 genomes]
rs2373848	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28691083	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35662160	0.81[ASN][1000 genomes]
rs4725927	0.87[EUR][1000 genomes]
rs55821597	0.88[ASN][1000 genomes]
rs62490381	0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6464095	0.82[EUR][1000 genomes]
rs6953961	0.88[ASN][1000 genomes]
rs6978377	0.83[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1034409	chr7:149844639-150447071	Flanking Active TSS Active TSS Genic enhancers Enhancers ZNF genes & repeats Bivalent Enhancer Weak transcription Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	75 gene(s)	inside rSNPs	diseases
2	nsv608990	chr7:149961274-150707488	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Weak transcription ZNF genes & repeats Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	90 gene(s)	inside rSNPs	diseases
3	nsv1017368	chr7:150016952-150655773	Bivalent Enhancer ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Strong transcription Active TSS Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	80 gene(s)	inside rSNPs	diseases
4	nsv539195	chr7:150016952-150655773	Bivalent Enhancer Weak transcription Flanking Active TSS Enhancers Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	80 gene(s)	inside rSNPs	diseases
5	esv2758617	chr7:150251949-150463804	Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS Active TSS Weak transcription Bivalent Enhancer Enhancers ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
6	esv2759573	chr7:150251949-150463804	Weak transcription Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
7	esv3388935	chr7:150301204-150374532	Enhancers Flanking Active TSS Weak transcription Active TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
8	nsv1030109	chr7:150312916-150701010	Enhancers Active TSS Weak transcription Bivalent Enhancer ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
9	nsv967475	chr7:150323577-150610034	Enhancers Bivalent Enhancer Weak transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
10	nsv831187	chr7:150325913-150503500	Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Genic enhancers Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs10225427	GIMAP2	Cis_1M	lymphoblastoid	RTeQTL
rs10225427	GIMAP6	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:21 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:150366000-150372800	Weak transcription	Thymus	Thymus
2	chr7:150368400-150372000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
3	chr7:150369000-150372000	Weak transcription	Primary T cells fromperipheralblood	blood
4	chr7:150369000-150372000	Weak transcription	Primary hematopoietic stem cells	blood
5	chr7:150369000-150372000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
6	chr7:150369000-150372000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
7	chr7:150369000-150372000	Weak transcription	Fetal Thymus	thymus
8	chr7:150370000-150373400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
9	chr7:150370000-150377000	Enhancers	Primary T helper cells fromperipheralblood	blood
10	chr7:150370600-150372000	Weak transcription	Primary T cells from cord blood	blood
11	chr7:150370600-150372000	Enhancers	Primary T helper naive cells from peripheral blood	blood
12	chr7:150370600-150372000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
13	chr7:150370600-150372000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
14	chr7:150370600-150372000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
15	chr7:150370600-150372200	Weak transcription	Adipose Nuclei	Adipose
16	chr7:150370800-150371800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
17	chr7:150370800-150372000	Weak transcription	Primary T helper cells PMA-I stimulated	--
18	chr7:150371200-150371800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
19	chr7:150371400-150371800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
20	chr7:150371400-150371800	Weak transcription	Dnd41	blood
21	chr7:150371600-150372800	Enhancers	Primary T killer memory cells from peripheral blood	blood

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