Variant report

Variant	rs34767748
Chromosome Location	chr12:76027164-76027165
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr12:76001058..76002737-chr12:76026565..76029545,2	K562	blood:
2	chr12:76019985..76022320-chr12:76024831..76027786,2	MCF-7	breast:
3	chr12:76014354..76029119-chr12:76417641..76428409,36	MCF-7	breast:

Variant related genes	Relation type
ENSG00000257453	Chromatin interaction
ENSG00000257839	Chromatin interaction
ENSG00000139289	Chromatin interaction

Extended variants
information (count: 38 )
Associated
traits (count: 4 )

rSNPs within LD-proxies of this variant (count:33)

rs_ID	r²[population]
rs10748283	0.80[ASN][1000 genomes]
rs10748284	0.96[ASN][1000 genomes]
rs10785199	0.82[ASN][1000 genomes]
rs10785200	0.82[ASN][1000 genomes]
rs10879937	0.80[ASN][1000 genomes]
rs10879943	0.81[AMR][1000 genomes];0.94[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs10879944	0.96[AFR][1000 genomes];0.99[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10879945	0.93[ASN][1000 genomes]
rs10879946	0.97[AFR][1000 genomes];0.99[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10879947	0.97[AMR][1000 genomes];0.93[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs10879948	0.86[AFR][1000 genomes];0.99[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11180600	0.81[AMR][1000 genomes];0.95[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs11180601	0.94[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11180605	0.95[ASN][1000 genomes]
rs12310185	0.97[AFR][1000 genomes];0.99[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12318049	0.81[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs1466464	0.91[AFR][1000 genomes];0.95[ASN][1000 genomes]
rs1871548	0.98[AFR][1000 genomes];0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs34952545	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4882601	0.98[AFR][1000 genomes];0.98[AMR][1000 genomes];0.94[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4882602	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4882637	0.98[AFR][1000 genomes];0.98[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4882639	0.99[AMR][1000 genomes];0.96[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4882640	0.97[AFR][1000 genomes];0.99[AMR][1000 genomes];0.96[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7137366	0.91[ASN][1000 genomes]
rs7958075	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7958490	0.98[AFR][1000 genomes];0.99[AMR][1000 genomes];0.94[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7958760	0.98[AFR][1000 genomes];0.99[AMR][1000 genomes];0.94[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7972231	0.85[ASN][1000 genomes]
rs7973399	0.98[AFR][1000 genomes];0.99[AMR][1000 genomes];0.94[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7980645	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs899658	0.94[ASN][1000 genomes]
rs899659	0.95[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv492067	chr12:75415458-76077537	Flanking Active TSS Enhancers Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
2	nsv1036987	chr12:75415532-76101559	Weak transcription Strong transcription Flanking Active TSS Enhancers Bivalent/Poised TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
3	nsv899313	chr12:75715330-76057811	Weak transcription Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Strong transcription Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
4	nsv1040583	chr12:75742802-76360276	Enhancers Genic enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
5	nsv948653	chr12:75773464-76220618	Active TSS Enhancers Flanking Active TSS Genic enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases

mRNA abundance (count:4)

SNP	Gene	Cis/trans	Tissue	Source
rs34767748	GLIPR1	Cis_1M	lymphoblastoid	RTeQTL
rs34767748	GLIPR1L2	cis	Skin Sun Exposed Lower leg	GTEx
rs34767748	GLIPR1L2	cis	Artery Tibial	GTEx
rs34767748	GLIPR1L2	cis	Thyroid	GTEx

Chromatin state (count:31 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:76017800-76028800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
2	chr12:76018000-76028600	Weak transcription	NHLF	lung
3	chr12:76018000-76028800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr12:76018200-76029600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
5	chr12:76018400-76027600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
6	chr12:76018400-76029400	Weak transcription	NHEK	skin
7	chr12:76023400-76028200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
8	chr12:76024000-76027800	Weak transcription	HepG2	liver
9	chr12:76024200-76028400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr12:76025000-76027800	Enhancers	HUES64 Cell Line	embryonic stem cell
11	chr12:76025000-76027800	Enhancers	iPS-18 Cell Line	embryonic stem cell
12	chr12:76025000-76028400	Enhancers	HUES48 Cell Line	embryonic stem cell
13	chr12:76025400-76030800	Enhancers	iPS-15b Cell Line	embryonic stem cell
14	chr12:76025600-76032400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr12:76025800-76027400	Weak transcription	H9 Cell Line	embryonic stem cell
16	chr12:76025800-76030200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
17	chr12:76026200-76027200	Enhancers	HUVEC	blood vessel
18	chr12:76026200-76030200	Enhancers	ES-I3 Cell Line	embryonic stem cell
19	chr12:76026400-76027600	Weak transcription	HUES6 Cell Line	embryonic stem cell
20	chr12:76026600-76028400	Weak transcription	Muscle Satellite Cultured Cells	--
21	chr12:76026600-76028600	Weak transcription	NH-A	brain
22	chr12:76026600-76028600	Weak transcription	NHDF-Ad	bronchial
23	chr12:76026600-76028800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
24	chr12:76026600-76029000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
25	chr12:76026600-76035000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
26	chr12:76026800-76027400	Enhancers	iPS-20b Cell Line	embryonic stem cell
27	chr12:76026800-76028200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr12:76027000-76027400	Weak transcription	Fetal Lung	lung
29	chr12:76027000-76028800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr12:76027000-76029600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr12:76027000-76029600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived

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