Variant report

Variant	rs4599829
Chromosome Location	chr8:19358434-19358435
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr8:19352728..19355401-chr8:19358201..19360523,2	K562	blood:

Extended variants
information (count: 111 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:100)

rs_ID	r²[population]
rs10105097	1.00[CHB][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs10105464	0.82[ASN][1000 genomes]
rs10503653	0.89[JPT][hapmap]
rs10888165	0.92[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs11204045	1.00[JPT][hapmap]
rs11204046	1.00[JPT][hapmap];0.85[ASN][1000 genomes]
rs11204047	1.00[JPT][hapmap];0.87[ASN][1000 genomes]
rs11204048	0.86[ASN][1000 genomes]
rs11204049	0.88[ASN][1000 genomes]
rs11204050	1.00[JPT][hapmap];0.88[ASN][1000 genomes]
rs11204052	0.98[ASN][1000 genomes]
rs11778734	0.89[JPT][hapmap]
rs11780475	0.90[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11783263	0.92[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs11786904	0.83[ASN][1000 genomes]
rs12682196	0.89[JPT][hapmap];0.83[ASN][1000 genomes]
rs13250181	0.89[JPT][hapmap];0.83[ASN][1000 genomes]
rs13261442	1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs13261732	0.82[CEU][hapmap];0.89[JPT][hapmap];0.82[ASN][1000 genomes]
rs13265751	1.00[JPT][hapmap];0.84[ASN][1000 genomes]
rs13266857	0.92[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs13267265	0.83[ASN][1000 genomes]
rs13267569	0.83[ASN][1000 genomes]
rs13267801	0.83[ASN][1000 genomes]
rs13275706	0.83[ASN][1000 genomes]
rs13276417	1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs13280711	0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs17128525	0.92[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs17479777	1.00[JPT][hapmap];0.88[ASN][1000 genomes]
rs28671342	0.98[ASN][1000 genomes]
rs3185	0.89[JPT][hapmap];0.83[ASN][1000 genomes]
rs3923920	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4073790	0.99[ASN][1000 genomes]
rs4073791	0.88[AFR][1000 genomes];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4244453	0.93[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.80[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs4273861	0.95[ASN][1000 genomes]
rs4292704	0.89[JPT][hapmap];0.83[ASN][1000 genomes]
rs4311666	0.89[JPT][hapmap]
rs4317590	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4319111	1.00[JPT][hapmap];0.82[ASN][1000 genomes]
rs4339658	0.96[ASN][1000 genomes]
rs4413788	1.00[JPT][hapmap];0.82[ASN][1000 genomes]
rs4442163	0.84[ASN][1000 genomes]
rs4455848	1.00[JPT][hapmap];0.86[ASN][1000 genomes]
rs4483172	1.00[JPT][hapmap];0.89[ASN][1000 genomes]
rs4484715	0.92[CEU][hapmap];0.92[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.91[AFR][1000 genomes];0.99[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4513991	0.88[ASN][1000 genomes]
rs4554481	1.00[JPT][hapmap];0.91[ASN][1000 genomes]
rs4614013	0.85[ASN][1000 genomes]
rs4631482	0.89[ASN][1000 genomes]
rs4631483	0.93[CEU][hapmap];1.00[CHB][hapmap];0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4921647	0.89[JPT][hapmap]
rs4921648	0.89[JPT][hapmap]
rs4921649	0.89[JPT][hapmap]
rs4921651	1.00[JPT][hapmap];0.84[ASN][1000 genomes]
rs4921652	0.83[ASN][1000 genomes]
rs4921653	0.92[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs4921654	0.92[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs4921655	0.98[ASN][1000 genomes]
rs4921656	0.92[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs4921657	1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs4922035	0.83[ASN][1000 genomes]
rs4922036	0.89[JPT][hapmap];0.83[ASN][1000 genomes]
rs4922037	0.82[ASN][1000 genomes]
rs4922038	0.84[ASN][1000 genomes]
rs4922039	0.84[ASN][1000 genomes]
rs4922041	0.85[ASN][1000 genomes]
rs4922044	1.00[JPT][hapmap];0.88[ASN][1000 genomes]
rs4922045	1.00[JPT][hapmap];0.89[ASN][1000 genomes]
rs4922046	1.00[JPT][hapmap];0.89[ASN][1000 genomes]
rs4922047	1.00[JPT][hapmap];0.89[ASN][1000 genomes]
rs4922048	1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[YRI][hapmap];1.00[ASN][1000 genomes]
rs4922049	1.00[JPT][hapmap];0.87[ASN][1000 genomes]
rs6586837	0.89[JPT][hapmap]
rs6586839	0.93[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs6586840	0.92[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs6984449	0.89[JPT][hapmap];0.83[ASN][1000 genomes]
rs6984644	0.92[CHB][hapmap];1.00[JPT][hapmap];0.83[YRI][hapmap];0.80[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs6986388	0.83[ASN][1000 genomes]
rs6988743	0.96[ASN][1000 genomes]
rs6991941	1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs6994352	0.89[JPT][hapmap]
rs6998334	1.00[JPT][hapmap];0.86[ASN][1000 genomes]
rs6998991	0.84[ASN][1000 genomes]
rs6999542	1.00[JPT][hapmap];0.88[ASN][1000 genomes]
rs7005075	0.93[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs7006155	0.83[ASN][1000 genomes]
rs7017776	1.00[JPT][hapmap];0.88[ASN][1000 genomes]
rs7460541	0.84[ASN][1000 genomes]
rs7464357	0.87[ASN][1000 genomes]
rs7464358	0.87[ASN][1000 genomes]
rs7816777	1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs7818691	0.89[JPT][hapmap];0.88[ASN][1000 genomes]
rs7828197	0.99[ASN][1000 genomes]
rs7830404	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs7839041	0.89[JPT][hapmap]
rs9644628	0.96[ASN][1000 genomes]
rs9644629	0.96[ASN][1000 genomes]
rs9644630	0.94[ASN][1000 genomes]
rs9644631	1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1015395	chr8:18489538-19370258	Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
2	nsv429907	chr8:18578720-19398220	Active TSS Weak transcription Enhancers Strong transcription Genic enhancers Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
3	nsv949745	chr8:18826830-19363963	Flanking Active TSS Enhancers Weak transcription Strong transcription Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
4	nsv533109	chr8:18845845-19456780	Weak transcription Flanking Active TSS Enhancers Strong transcription Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
5	nsv949636	chr8:18957705-19664732	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer 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	18 gene(s)	inside rSNPs	diseases
6	nsv948861	chr8:19199688-19609029	Strong transcription Enhancers Weak transcription Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
7	nsv949304	chr8:19199688-19625912	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases
8	esv3693374	chr8:19241970-19359184	Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region miRNA target site	2 gene(s)	inside rSNPs	diseases
9	esv34007	chr8:19252602-19482098	Enhancers Weak transcription ZNF genes & repeats Genic enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	3 gene(s)	inside rSNPs	diseases
10	nsv890623	chr8:19307051-19383697	Weak transcription Enhancers Genic enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
11	nsv890624	chr8:19319061-19456270	Enhancers Weak transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Strong transcription Bivalent/Poised TSS Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs4599829	CSGALNACT1	cis	Thyroid	GTEx

Chromatin state (count:59 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:19310600-19359600	Weak transcription	Ovary	ovary
2	chr8:19319600-19362800	Weak transcription	Spleen	Spleen
3	chr8:19333400-19362200	Weak transcription	Primary B cells from peripheral blood	blood
4	chr8:19338800-19370600	Weak transcription	Esophagus	oesophagus
5	chr8:19348000-19376600	Weak transcription	Pancreatic Islets	Pancreatic Islet
6	chr8:19348200-19364000	Weak transcription	Brain Hippocampus Middle	brain
7	chr8:19348200-19367400	Weak transcription	Fetal Brain Female	brain
8	chr8:19348600-19359000	Weak transcription	Fetal Brain Male	brain
9	chr8:19350200-19362800	Weak transcription	Gastric	stomach
10	chr8:19351200-19369000	Weak transcription	Primary monocytes fromperipheralblood	blood
11	chr8:19353200-19362200	Weak transcription	Adipose Nuclei	Adipose
12	chr8:19353400-19359600	Weak transcription	Brain Cingulate Gyrus	brain
13	chr8:19353400-19367600	Weak transcription	Brain Anterior Caudate	brain
14	chr8:19353400-19367600	Weak transcription	Brain Inferior Temporal Lobe	brain
15	chr8:19354400-19367800	Weak transcription	Brain Substantia Nigra	brain
16	chr8:19354600-19359600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
17	chr8:19354600-19360600	Enhancers	Primary T helper cells fromperipheralblood	blood
18	chr8:19354600-19361400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
19	chr8:19354600-19362600	Weak transcription	Lung	lung
20	chr8:19354800-19360000	Enhancers	Primary T cells fromperipheralblood	blood
21	chr8:19354800-19362600	Weak transcription	Pancreas	Pancrea
22	chr8:19354800-19366000	Weak transcription	Brain Angular Gyrus	brain
23	chr8:19355000-19358800	Enhancers	Placenta	Placenta
24	chr8:19355000-19359000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
25	chr8:19355000-19359400	Weak transcription	Fetal Heart	heart
26	chr8:19355000-19362600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
27	chr8:19355200-19363200	Weak transcription	Primary hematopoietic stem cells	blood
28	chr8:19355400-19358600	Enhancers	Primary T cells from cord blood	blood
29	chr8:19355400-19361200	Enhancers	Primary T helper cells PMA-I stimulated	--
30	chr8:19355600-19358600	Enhancers	Primary T helper naive cells from peripheral blood	blood
31	chr8:19355800-19367600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
32	chr8:19356000-19359000	Weak transcription	Fetal Stomach	stomach
33	chr8:19356000-19368400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
34	chr8:19356200-19358600	Genic enhancers	Primary T regulatory cells fromperipheralblood	blood
35	chr8:19356200-19359000	Weak transcription	Right Ventricle	heart
36	chr8:19356200-19362400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
37	chr8:19356400-19362200	Weak transcription	Skeletal Muscle Male	skeletal muscle
38	chr8:19356400-19368600	Weak transcription	Thymus	Thymus
39	chr8:19356800-19362600	Weak transcription	Aorta	Aorta
40	chr8:19357200-19360000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
41	chr8:19357600-19358600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
42	chr8:19357800-19358600	Weak transcription	Fetal Lung	lung
43	chr8:19357800-19359400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
44	chr8:19357800-19359600	Enhancers	NHLF	lung
45	chr8:19357800-19362600	Weak transcription	Placenta Amnion	Placenta Amnion
46	chr8:19357800-19362800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
47	chr8:19358000-19359000	Weak transcription	Primary neutrophils fromperipheralblood	blood
48	chr8:19358000-19359000	Weak transcription	Right Atrium	heart
49	chr8:19358000-19359600	Weak transcription	Fetal Thymus	thymus
50	chr8:19358000-19359800	Enhancers	NHDF-Ad	bronchial

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