Variant report

Variant	rs1600100
Chromosome Location	chr4:76402611-76402612
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 47 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:45)

rs_ID	r²[population]
rs10029348	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10031553	0.86[AMR][1000 genomes];0.86[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1046662	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11728327	0.85[AMR][1000 genomes];0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11730978	0.87[AMR][1000 genomes];0.87[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11735018	0.85[AMR][1000 genomes];0.85[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11935932	0.90[EUR][1000 genomes]
rs13112378	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs13145288	0.86[AMR][1000 genomes];0.86[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1351092	0.94[EUR][1000 genomes]
rs1389443	0.94[EUR][1000 genomes]
rs1395359	0.81[EUR][1000 genomes]
rs1395360	0.81[EUR][1000 genomes]
rs1478174	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1564174	0.93[EUR][1000 genomes]
rs1580297	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1676917	0.94[EUR][1000 genomes]
rs1817387	0.86[AMR][1000 genomes];0.84[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1841932	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1841934	0.84[AMR][1000 genomes];0.84[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2045863	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2126855	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs28507535	0.88[AMR][1000 genomes];0.84[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2867920	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2867921	0.87[AMR][1000 genomes];0.87[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4593160	0.84[EUR][1000 genomes]
rs4859963	0.85[EUR][1000 genomes]
rs59581284	0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6535523	0.83[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6815241	0.86[AMR][1000 genomes];0.84[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs6816603	0.86[AMR][1000 genomes];0.85[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs6823674	0.94[AMR][1000 genomes];0.90[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6829753	0.89[AMR][1000 genomes];0.85[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs6833496	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs6835579	0.89[AMR][1000 genomes];0.84[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs6841171	0.81[EUR][1000 genomes]
rs6841882	0.87[AMR][1000 genomes];0.87[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7661659	0.86[AMR][1000 genomes];0.85[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7664140	0.89[AMR][1000 genomes];0.85[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7698352	0.94[AMR][1000 genomes];0.92[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs786682	0.94[EUR][1000 genomes]
rs786684	0.94[EUR][1000 genomes]
rs9041	0.85[AMR][1000 genomes];0.84[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs949611	0.84[EUR][1000 genomes]
rs955545	0.85[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv594687	chr4:76154064-76502748	Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Enhancers Strong transcription Genic enhancers Bivalent Enhancer 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	27 gene(s)	inside rSNPs	diseases
2	nsv534570	chr4:76214619-76498362	ZNF genes & repeats Flanking Active TSS Strong transcription Weak transcription Enhancers Active TSS Genic enhancers Bivalent Enhancer 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
rs1600100	THAP6	cis	multi-tissue	Pritchard

Chromatin state (count:111 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:76392600-76434800	Weak transcription	Gastric	stomach
2	chr4:76392800-76403000	Weak transcription	Fetal Brain Female	brain
3	chr4:76394000-76406200	Weak transcription	Colon Smooth Muscle	Colon
4	chr4:76394000-76406600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
5	chr4:76394600-76424600	Weak transcription	Right Ventricle	heart
6	chr4:76395400-76405200	Weak transcription	Fetal Heart	heart
7	chr4:76395600-76405800	Weak transcription	Brain Germinal Matrix	brain
8	chr4:76395800-76406600	Weak transcription	Placenta Amnion	Placenta Amnion
9	chr4:76395800-76437000	Weak transcription	Aorta	Aorta
10	chr4:76395800-76437000	Weak transcription	Lung	lung
11	chr4:76395800-76437000	Weak transcription	Pancreas	Pancrea
12	chr4:76396200-76424400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
13	chr4:76396200-76437000	Weak transcription	Esophagus	oesophagus
14	chr4:76396600-76403600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
15	chr4:76397000-76403200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
16	chr4:76397000-76403400	Weak transcription	Duodenum Smooth Muscle	Duodenum
17	chr4:76397000-76403600	Weak transcription	Skeletal Muscle Female	skeletal muscle
18	chr4:76397000-76405200	Weak transcription	NHEK	skin
19	chr4:76397200-76403600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
20	chr4:76397200-76403800	Weak transcription	HUVEC	blood vessel
21	chr4:76397200-76405200	Weak transcription	Left Ventricle	heart
22	chr4:76397200-76414600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
23	chr4:76397400-76403000	Weak transcription	Muscle Satellite Cultured Cells	--
24	chr4:76397400-76403600	Weak transcription	NH-A	brain
25	chr4:76397400-76403800	Weak transcription	GM12878-XiMat	blood
26	chr4:76397800-76437000	Weak transcription	H9 Cell Line	embryonic stem cell
27	chr4:76398000-76403600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
28	chr4:76398200-76405600	Weak transcription	Sigmoid Colon	Sigmoid Colon
29	chr4:76398200-76415800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
30	chr4:76398200-76434200	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
31	chr4:76398400-76407400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
32	chr4:76398600-76403600	Weak transcription	NHDF-Ad	bronchial
33	chr4:76398600-76405600	Weak transcription	NHLF	lung
34	chr4:76398800-76437200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
35	chr4:76399400-76434400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
36	chr4:76400600-76403600	Weak transcription	Brain Cingulate Gyrus	brain
37	chr4:76400600-76403800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
38	chr4:76400600-76437000	Weak transcription	Spleen	Spleen
39	chr4:76400800-76404800	Weak transcription	Cortex derived primary cultured neurospheres	brain
40	chr4:76400800-76405200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
41	chr4:76400800-76405200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
42	chr4:76400800-76405600	Weak transcription	Fetal Muscle Trunk	muscle
43	chr4:76400800-76406600	Weak transcription	HMEC	breast
44	chr4:76400800-76409200	Weak transcription	Thymus	Thymus
45	chr4:76401000-76405400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
46	chr4:76401000-76405400	Weak transcription	Colonic Mucosa	Colon
47	chr4:76401000-76406600	Weak transcription	Hela-S3	cervix
48	chr4:76401000-76410800	Weak transcription	HSMMtube	muscle
49	chr4:76401000-76436200	Weak transcription	Brain Angular Gyrus	brain
50	chr4:76401200-76403800	Weak transcription	Fetal Intestine Large	intestine

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