Variant report

Variant	rs57987061
Chromosome Location	chr3:46761603-46761604
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:61)
Chromatin interactive
region (count:1)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:46761555-46761605	NT2-D1	testis:	n/a
2	chr3:46761555-46761605	BE2_C	brain:	n/a
3	chr3:46761555-46761605	HL-60	blood:	n/a
4	chr3:46761555-46761605	HPAEpiC	pulmonary alveolar:	n/a
5	chr3:46761555-46761605	AG04449	skin:	fetal
6	chr3:46761555-46761605	HRCEpiC	kidney:	n/a
7	chr3:46761555-46761605	Hepatocyte	liver:	n/a
8	chr3:46761555-46761605	SK-N-SH	brain:	n/a
9	chr3:46761555-46761605	HepG2	liver:	n/a
10	chr3:46761555-46761605	ProgFib	skin:	n/a
11	chr3:46761555-46761605	RPTEC	kidney:	n/a
12	chr3:46761555-46761605	IMR90	lung:	fetal
13	chr3:46761555-46761605	GM12878	blood:	n/a
14	chr3:46761555-46761605	AoSMC	blood vessel:	n/a
15	chr3:46761555-46761605	AG09319	gingival:	n/a
16	chr3:46761555-46761605	HUVEC	blood vessel:	n/a
17	chr3:46761555-46761605	SKMC	muscle:	n/a
18	chr3:46761555-46761605	SAEC	small airway:	n/a
19	chr3:46761555-46761605	MCF10A-Er-Src	breast:	n/a
20	chr3:46761555-46761605	H1-hESC	embryonic stem cell:	embryo
21	chr3:46761555-46761605	GM12891	blood:	n/a
22	chr3:46761555-46761605	HCPEpiC	choroid plexus:	n/a
23	chr3:46761555-46761605	MCF-7	breast:	n/a
24	chr3:46761555-46761605	U87	brain:	n/a
25	chr3:46761555-46761605	Hela-S3	cervix:	n/a
26	chr3:46761555-46761605	HCT-116	colon:	n/a
27	chr3:46761555-46761605	CMK	blood:	n/a
28	chr3:46761555-46761605	ovcar-3	ovarian:	n/a
29	chr3:46761555-46761605	NHDF-neo	bronchial:	n/a
30	chr3:46761555-46761605	AG10803	skin:	n/a
31	chr3:46761555-46761605	HNPCEpiC	eye:	n/a
32	chr3:46761555-46761605	HIPEpiC	eye:	n/a
33	chr3:46761555-46761605	HCM	heart:	n/a
34	chr3:46761555-46761605	NB4	blood:	n/a
35	chr3:46761555-46761605	A549	lung:	n/a
36	chr3:46761555-46761605	ECC-1	luminal epithelium:	n/a
37	chr3:46761555-46761605	T-47D	breast:	n/a
38	chr3:46761555-46761605	HRE	kidney:	n/a
39	chr3:46761555-46761605	HRPEpiC	eye:	n/a
40	chr3:46761555-46761605	HMEC	breast:	n/a
41	chr3:46761555-46761605	HEEpiC	esophagus:	n/a
42	chr3:46761555-46761605	GM06990	blood:	n/a
43	chr3:46761555-46761605	AG04450	lung:	fetal
44	chr3:46761555-46761605	SK-N-MC	brain:	n/a
45	chr3:46761555-46761605	Caco-2	colon:	n/a
46	chr3:46761555-46761605	PrEC	prostate:	n/a
47	chr3:46761555-46761605	LNCaP	prostate:	n/a
48	chr3:46761555-46761605	HAEpiC	amniotic membrane:	n/a
49	chr3:46761555-46761605	PFSK-1	brain:	n/a
50	chr3:46761555-46761605	HEK293	kidney:	embryo

(count:1 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr3:46760704..46762742-chr3:47031242..47033337,2	K562	blood:

No data

Variant related genes	Relation type
PRSS50	CpG island

Extended variants
information (count: 51 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:35)

rs_ID	r²[population]
rs12485284	0.81[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs12489661	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12489663	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12492946	1.00[ASN][1000 genomes]
rs12496832	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs55712958	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56208931	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs56752770	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs58137727	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs59529839	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs59618012	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs59637204	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs60132352	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs60643068	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs61038123	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs66736629	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6793235	0.89[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs6793535	0.85[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs6793661	0.85[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs6808303	0.85[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs68175547	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs72899400	0.85[AMR][1000 genomes];0.97[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs73063653	0.98[ASN][1000 genomes]
rs73063655	1.00[ASN][1000 genomes]
rs73063668	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs73063682	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs73063683	0.97[ASN][1000 genomes]
rs73063688	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7428736	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7428787	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7623501	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7626129	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7632176	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7632771	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7639979	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:16 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1007449	chr3:46652343-46986578	Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3' Enhancers ZNF genes & repeats Genic enhancers Strong transcription Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	30 gene(s)	inside rSNPs	diseases
2	nsv536554	chr3:46652343-46986578	Enhancers Weak transcription Bivalent Enhancer Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS ZNF genes & repeats Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	30 gene(s)	inside rSNPs	diseases
3	nsv876741	chr3:46663372-46763839	Enhancers Flanking Active TSS Weak transcription Strong transcription Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
4	nsv516623	chr3:46680063-46852679	Enhancers Strong transcription Genic enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
5	esv2757869	chr3:46680452-46972489	Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Weak transcription Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
6	esv2759147	chr3:46680452-46972489	Genic enhancers Flanking Active TSS Enhancers Strong transcription Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
7	esv1804680	chr3:46704348-46869911	Bivalent Enhancer Flanking Active TSS Weak transcription Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh Strong transcription Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
8	nsv876742	chr3:46705369-46763839	Flanking Bivalent TSS/Enh Enhancers Weak transcription Bivalent Enhancer Genic enhancers Active TSS Flanking Active TSS Strong transcription Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	16 gene(s)	inside rSNPs	diseases
9	nsv536555	chr3:46706571-46817963	Flanking Active TSS Strong transcription Genic enhancers Bivalent Enhancer Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
10	nsv536556	chr3:46706571-46849443	Genic enhancers Bivalent/Poised TSS Weak transcription Enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
11	nsv536557	chr3:46706571-46853434	Bivalent Enhancer Flanking Active TSS Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Enhancers Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
12	nsv536558	chr3:46706571-47024756	Enhancers Bivalent Enhancer Active TSS Strong transcription Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	35 gene(s)	inside rSNPs	diseases
13	nsv876744	chr3:46716523-46763839	Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Strong transcription ZNF genes & repeats Active TSS Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	15 gene(s)	inside rSNPs	diseases
14	nsv460525	chr3:46728659-46790397	Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Active TSS Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	17 gene(s)	inside rSNPs	diseases
15	nsv590179	chr3:46728659-46790397	Flanking Bivalent TSS/Enh Active TSS Weak transcription Bivalent Enhancer Flanking Active TSS Enhancers Bivalent/Poised TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	17 gene(s)	inside rSNPs	diseases
16	nsv876745	chr3:46753976-46884552	Enhancers Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs57987061	PRSS46	cis	Thyroid	GTEx
rs57987061	PRSS46	cis	Heart Left Ventricle	GTEx

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:46744000-46792200	Weak transcription	Right Atrium	heart
2	chr3:46760000-46761800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
3	chr3:46761000-46766200	Weak transcription	Placenta Amnion	Placenta Amnion
4	chr3:46761600-46761800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell

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