Variant report

Variant	rs16941544
Chromosome Location	chr15:59934120-59934121
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr15:59931535..59934345-chr15:59941225..59942727,2	K562	blood:
2	chr15:59927646..59929889-chr15:59932303..59934645,2	K562	blood:

Extended variants
information (count: 38 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:32)

rs_ID	r²[population]
rs12050786	0.96[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs12161993	0.82[JPT][hapmap]
rs17236713	0.93[CHB][hapmap];1.00[JPT][hapmap];0.81[YRI][hapmap];0.84[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs17236734	0.93[CHB][hapmap];0.89[JPT][hapmap];0.84[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs17302448	0.93[CHB][hapmap];1.00[JPT][hapmap];0.93[YRI][hapmap];0.88[AFR][1000 genomes];0.84[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs17302608	0.83[JPT][hapmap]
rs28395445	0.96[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs28418513	0.84[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs28422085	0.84[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs28437066	0.88[AFR][1000 genomes];0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs28642859	0.84[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs28654927	0.93[ASN][1000 genomes]
rs28883924	0.92[ASN][1000 genomes]
rs4775192	0.93[CHB][hapmap];1.00[JPT][hapmap];0.90[YRI][hapmap];0.88[AFR][1000 genomes];0.84[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4775193	0.86[CHB][hapmap];0.94[JPT][hapmap];0.93[YRI][hapmap];0.84[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4775198	0.90[AFR][1000 genomes];0.96[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs6151443	0.83[JPT][hapmap];0.81[YRI][hapmap]
rs6151457	0.95[JPT][hapmap];1.00[YRI][hapmap];0.85[AMR][1000 genomes]
rs6151492	0.85[AMR][1000 genomes]
rs6151497	0.89[JPT][hapmap];0.93[YRI][hapmap];0.85[AMR][1000 genomes]
rs6151505	0.89[AMR][1000 genomes]
rs6151522	0.96[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs6151534	0.94[JPT][hapmap];0.93[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs6151538	0.90[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs6151540	0.90[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs6151567	0.93[CHB][hapmap];0.89[JPT][hapmap];0.90[YRI][hapmap];0.84[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6151575	0.90[AFR][1000 genomes];0.84[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6151591	0.93[CHB][hapmap];0.88[JPT][hapmap];0.89[YRI][hapmap];0.85[AFR][1000 genomes];0.84[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs8026404	0.81[YRI][hapmap]
rs8027421	0.85[AFR][1000 genomes];0.89[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs8033208	0.81[CHB][hapmap];0.95[JPT][hapmap];0.89[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs8033718	0.88[AFR][1000 genomes];0.89[EUR][1000 genomes];0.95[ASN][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	nsv527307	chr15:59103328-60018487	Enhancers Genic enhancers Weak transcription Flanking Bivalent TSS/Enh Strong transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	145 gene(s)	inside rSNPs	diseases
2	nsv1044442	chr15:59765724-59955587	Weak transcription Enhancers Active TSS ZNF genes & repeats Strong transcription Flanking Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
3	nsv542403	chr15:59765724-59955587	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
4	nsv569605	chr15:59855226-59956553	Strong transcription Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
5	nsv533240	chr15:59858093-59998176	Flanking Active TSS Strong transcription Enhancers Weak transcription Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
6	esv1824522	chr15:59919844-59987181	Weak transcription Enhancers Active TSS Strong transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs16941544	GCNT3	cis	multi-tissue	Pritchard

Chromatin state (count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:59905200-59946200	Weak transcription	Gastric	stomach
2	chr15:59912200-59935000	Weak transcription	Fetal Intestine Small	intestine
3	chr15:59914800-59937800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr15:59920600-59947000	Weak transcription	Small Intestine	intestine
5	chr15:59925000-59936800	Weak transcription	H9 Cell Line	embryonic stem cell
6	chr15:59925000-59936800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
7	chr15:59925000-59943800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
8	chr15:59925400-59937200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
9	chr15:59925600-59936600	Weak transcription	NHLF	lung
10	chr15:59925600-59937800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
11	chr15:59925600-59948600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
12	chr15:59925800-59936600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
13	chr15:59925800-59943800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
14	chr15:59926200-59936800	Weak transcription	Fetal Brain Male	brain
15	chr15:59926200-59937000	Weak transcription	Placenta Amnion	Placenta Amnion
16	chr15:59926400-59935800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
17	chr15:59926400-59936600	Weak transcription	Brain Inferior Temporal Lobe	brain
18	chr15:59926600-59936600	Weak transcription	Brain Cingulate Gyrus	brain
19	chr15:59926600-59944000	Weak transcription	Fetal Kidney	kidney
20	chr15:59926600-59947600	Weak transcription	Right Ventricle	heart
21	chr15:59926600-59948000	Weak transcription	Brain Angular Gyrus	brain
22	chr15:59927000-59937000	Weak transcription	Lung	lung
23	chr15:59927200-59936600	Weak transcription	HMEC	breast
24	chr15:59927200-59948800	Weak transcription	Aorta	Aorta
25	chr15:59927400-59943800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr15:59927600-59936200	Weak transcription	Pancreas	Pancrea
27	chr15:59927800-59942800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
28	chr15:59928000-59934600	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr15:59928200-59934600	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
30	chr15:59928200-59934600	Strong transcription	Primary T helper cells PMA-I stimulated	--
31	chr15:59928400-59934400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
32	chr15:59928400-59934800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
33	chr15:59928400-59935000	Strong transcription	Primary B cells from cord blood	blood
34	chr15:59928400-59936600	Weak transcription	Brain Anterior Caudate	brain
35	chr15:59928400-59940200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
36	chr15:59928400-59945600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
37	chr15:59928600-59935200	Strong transcription	Monocytes-CD14+_RO01746	blood
38	chr15:59928600-59936400	Weak transcription	HSMMtube	muscle
39	chr15:59928800-59934600	Strong transcription	Primary T helper cells fromperipheralblood	blood
40	chr15:59928800-59937400	Weak transcription	H1 Cell Line	embryonic stem cell
41	chr15:59928800-59942000	Weak transcription	Fetal Heart	heart
42	chr15:59929000-59936600	Weak transcription	Brain Substantia Nigra	brain
43	chr15:59929000-59936800	Weak transcription	Esophagus	oesophagus
44	chr15:59929000-59942200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr15:59929000-59944000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr15:59929000-59947200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
47	chr15:59929200-59936200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
48	chr15:59929200-59941400	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
49	chr15:59929200-59947600	Weak transcription	Ovary	ovary
50	chr15:59929400-59934400	Strong transcription	Adipose Nuclei	Adipose

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