Variant report

Variant	rs61828574
Chromosome Location	chr1:174165668-174165669
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr1:174157753..174160187-chr1:174164644..174167517,2	MCF-7	breast:
2	chr1:174128707..174130217-chr1:174164709..174166414,2	K562	blood:
3	chr1:174158960..174161694-chr1:174164662..174167169,2	K562	blood:
4	chr1:174045340..174046921-chr1:174165534..174168134,2	K562	blood:
5	chr1:174127383..174130207-chr1:174164914..174166564,2	K562	blood:

Variant related genes	Relation type
ENSG00000152061	Chromatin interaction
ENSG00000227373	Chromatin interaction

Extended variants
information (count: 61 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:53)

rs_ID	r²[population]
rs10127823	0.86[EUR][1000 genomes]
rs12562344	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12564848	0.81[AMR][1000 genomes];0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12564858	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12565675	0.84[AMR][1000 genomes];0.96[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12566643	0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12567854	0.81[AMR][1000 genomes];0.96[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12567864	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12737218	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1407126	0.90[EUR][1000 genomes]
rs16828467	0.90[EUR][1000 genomes]
rs16846667	0.86[EUR][1000 genomes]
rs16846688	0.90[EUR][1000 genomes]
rs1890881	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2015075	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs41265242	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs41266044	0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4140468	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs57651489	0.91[AMR][1000 genomes];0.90[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs58866024	0.97[AMR][1000 genomes];0.92[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs60005461	0.97[AMR][1000 genomes];0.92[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs60039606	0.87[EUR][1000 genomes]
rs61826829	0.82[EUR][1000 genomes]
rs61826831	0.82[EUR][1000 genomes]
rs61827889	0.90[EUR][1000 genomes]
rs61827900	0.84[EUR][1000 genomes]
rs61827901	0.92[EUR][1000 genomes]
rs61827902	0.92[EUR][1000 genomes]
rs61827903	0.92[EUR][1000 genomes]
rs61827904	0.95[EUR][1000 genomes]
rs61827905	0.97[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs61828571	0.97[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs61828575	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs61828576	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs61828577	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs61828578	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs61828580	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs61828583	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs61828584	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs61828587	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs61828589	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs61828590	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs61828591	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs61828592	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs61828595	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs61828622	0.81[AMR][1000 genomes];0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs61828624	0.91[AMR][1000 genomes];0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs61828625	0.81[AMR][1000 genomes];0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs61828627	0.87[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7525325	0.94[AFR][1000 genomes];0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7528644	0.82[AFR][1000 genomes]
rs965498	0.82[EUR][1000 genomes]
rs9970465	0.83[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv872552	chr1:174061844-174469748	Strong transcription Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	30 gene(s)	inside rSNPs	diseases
2	nsv1008314	chr1:174080192-174311023	Weak transcription Enhancers Strong transcription Active TSS ZNF genes & repeats Genic enhancers Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
3	nsv535207	chr1:174080192-174311023	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
4	esv1799250	chr1:174119038-174484277	Weak transcription Enhancers Genic enhancers Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	29 gene(s)	inside rSNPs	diseases
5	esv1800060	chr1:174132703-174501836	Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
6	nsv465672	chr1:174133251-174469905	Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
7	nsv548194	chr1:174133251-174469905	Enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
8	nsv470746	chr1:174150850-174469905	Strong transcription Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs61828574	SERPINC1	cis	Muscle Skeletal	GTEx

Chromatin state (count:32 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:174129600-174173200	Weak transcription	Pancreas	Pancrea
2	chr1:174144000-174178200	Weak transcription	Left Ventricle	heart
3	chr1:174154200-174173600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
4	chr1:174159800-174170200	Weak transcription	Fetal Intestine Small	intestine
5	chr1:174160000-174173600	Weak transcription	Primary B cells from peripheral blood	blood
6	chr1:174160600-174173800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
7	chr1:174160800-174169600	Weak transcription	Primary T helper cells fromperipheralblood	blood
8	chr1:174160800-174169800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
9	chr1:174160800-174186600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr1:174161000-174166400	Weak transcription	Fetal Heart	heart
11	chr1:174161000-174169000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
12	chr1:174161000-174169400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
13	chr1:174161000-174172200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
14	chr1:174161000-174172400	Weak transcription	Fetal Intestine Large	intestine
15	chr1:174161000-174173600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
16	chr1:174161000-174176200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
17	chr1:174161200-174176600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
18	chr1:174161600-174175000	Weak transcription	NHDF-Ad	bronchial
19	chr1:174161600-174178600	Weak transcription	Primary B cells from cord blood	blood
20	chr1:174161800-174173800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
21	chr1:174162000-174173800	Weak transcription	Hela-S3	cervix
22	chr1:174162000-174189600	Weak transcription	Duodenum Mucosa	Duodenum
23	chr1:174162400-174167400	Weak transcription	GM12878-XiMat	blood
24	chr1:174163800-174178200	Weak transcription	Primary hematopoietic stem cells	blood
25	chr1:174164000-174169400	Weak transcription	Primary T cells from cord blood	blood
26	chr1:174164000-174170400	Weak transcription	Primary T cells fromperipheralblood	blood
27	chr1:174164000-174173000	Weak transcription	Primary T helper cells PMA-I stimulated	--
28	chr1:174164000-174173000	Weak transcription	K562	blood
29	chr1:174164000-174173800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
30	chr1:174164200-174169200	Weak transcription	Dnd41	blood
31	chr1:174164200-174172200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
32	chr1:174164400-174168400	Weak transcription	Primary hematopoietic stem cells short term culture	blood

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