Variant report

Variant	rs4673532
Chromosome Location	chr2:211344115-211344116
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr2:211340873..211343591-chr2:211343599..211345221,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000115365	Chromatin interaction
ENSG00000021826	Chromatin interaction

Extended variants
information (count: 42 )
Associated
traits (count: 4 )

rSNPs within LD-proxies of this variant (count:41)

rs_ID	r²[population]
rs10932334	0.84[AMR][1000 genomes];0.90[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12464878	0.84[AFR][1000 genomes];0.88[AMR][1000 genomes];0.91[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs12474078	0.85[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs12618926	0.83[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs12623942	0.81[ASN][1000 genomes]
rs1396954	0.84[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs17552879	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2042049	0.84[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs2287417	0.84[AFR][1000 genomes];0.88[AMR][1000 genomes];0.90[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2287418	0.84[AMR][1000 genomes];0.90[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2287419	0.84[AFR][1000 genomes];0.88[AMR][1000 genomes];0.90[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2287420	0.84[AFR][1000 genomes];0.88[AMR][1000 genomes];0.90[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2287421	0.85[ASN][1000 genomes]
rs2287422	0.85[ASN][1000 genomes]
rs2370948	0.81[AFR][1000 genomes];0.86[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs3755182	0.84[AFR][1000 genomes];0.88[AMR][1000 genomes];0.91[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs3770685	0.85[ASN][1000 genomes]
rs3770687	0.81[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs3770690	0.85[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs3770691	0.85[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs3856340	0.83[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs3856342	0.83[ASN][1000 genomes]
rs3856343	0.89[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs3856344	0.87[EUR][1000 genomes]
rs3856345	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs3856346	0.83[AMR][1000 genomes];0.87[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs3856347	0.89[AFR][1000 genomes];0.87[AMR][1000 genomes];0.93[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs3856348	0.89[AFR][1000 genomes];0.88[AMR][1000 genomes];0.93[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs3856349	0.89[AFR][1000 genomes];0.87[AMR][1000 genomes];0.93[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4672577	0.89[AFR][1000 genomes];0.88[AMR][1000 genomes];0.92[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs4673530	0.85[ASN][1000 genomes]
rs4673531	0.89[AFR][1000 genomes];0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4673533	0.84[AFR][1000 genomes];0.88[AMR][1000 genomes];0.92[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs62203668	0.85[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs62203669	0.87[AMR][1000 genomes];0.88[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs62203670	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs62203672	0.81[AFR][1000 genomes];0.88[AMR][1000 genomes];0.91[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs62203673	0.84[AFR][1000 genomes];0.86[AMR][1000 genomes];0.91[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs62203674	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs62203675	0.89[AFR][1000 genomes];0.88[AMR][1000 genomes];0.93[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6727682	0.81[AMR][1000 genomes];0.88[EUR][1000 genomes];0.85[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3398091	chr2:211315261-211634200	Active TSS Flanking Active TSS Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases

mRNA abundance (count:4)

SNP	Gene	Cis/trans	Tissue	Source
rs4673532	LANCL1	Cis_1M	lymphoblastoid	RTeQTL
rs4673532	CPS1	cis	lung	GTEx
rs4673532	CPS1	cis	Artery Tibial	GTEx
rs4673532	CPS1	cis	Adipose Subcutaneous	GTEx

Chromatin state (count:40 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:211341600-211344800	Weak transcription	Spleen	Spleen
2	chr2:211341600-211347800	Weak transcription	Gastric	stomach
3	chr2:211341600-211348800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr2:211341600-211348800	Weak transcription	Pancreas	Pancrea
5	chr2:211341800-211345000	Weak transcription	Fetal Muscle Leg	muscle
6	chr2:211342200-211344800	Weak transcription	Pancreatic Islets	Pancreatic Islet
7	chr2:211342400-211344800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
8	chr2:211342400-211346400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
9	chr2:211342600-211344800	Weak transcription	Primary T cells fromperipheralblood	blood
10	chr2:211342600-211344800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
11	chr2:211342600-211346200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
12	chr2:211342600-211348000	Weak transcription	Fetal Intestine Small	intestine
13	chr2:211342800-211346200	Weak transcription	H1 Cell Line	embryonic stem cell
14	chr2:211342800-211346200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
15	chr2:211343000-211344800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
16	chr2:211343000-211344800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
17	chr2:211343000-211345800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
18	chr2:211343000-211346000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
19	chr2:211343000-211346200	Weak transcription	HUES48 Cell Line	embryonic stem cell
20	chr2:211343000-211355200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
21	chr2:211343200-211344800	Weak transcription	Primary T helper cells PMA-I stimulated	--
22	chr2:211343200-211344800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
23	chr2:211343200-211344800	Weak transcription	HMEC	breast
24	chr2:211343200-211345800	Weak transcription	Hela-S3	cervix
25	chr2:211343200-211346200	Weak transcription	HUES64 Cell Line	embryonic stem cell
26	chr2:211343200-211348000	Weak transcription	Ovary	ovary
27	chr2:211343400-211344600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
28	chr2:211343400-211344800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
29	chr2:211343400-211344800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
30	chr2:211343400-211346600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
31	chr2:211343400-211347800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr2:211343400-211363600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
33	chr2:211343600-211344800	Weak transcription	NHEK	skin
34	chr2:211343600-211346200	Weak transcription	HUES6 Cell Line	embryonic stem cell
35	chr2:211343800-211346400	Weak transcription	HSMM	muscle
36	chr2:211344000-211344800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
37	chr2:211344000-211344800	Weak transcription	Primary T helper cells fromperipheralblood	blood
38	chr2:211344000-211344800	Weak transcription	K562	blood
39	chr2:211344000-211348800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
40	chr2:211344000-211350800	Weak transcription	Breast Myoepithelial Primary Cells	Breast

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