Variant report

Variant	rs2162797
Chromosome Location	chr19:18601016-18601017
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:8)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:18596615..18599605-chr19:18599689..18601535,3	K562	blood:
2	chr19:18599505..18602337-chr19:18612086..18613638,2	MCF-7	breast:
3	chr19:18578145..18580675-chr19:18600107..18604361,3	MCF-7	breast:
4	chr19:18597781..18601216-chr19:18667431..18670376,3	MCF-7	breast:
5	chr19:18600195..18604432-chr19:18699323..18701872,3	K562	blood:
6	chr19:18581749..18584173-chr19:18598767..18601257,2	K562	blood:
7	chr19:18597905..18599605-chr19:18599689..18601535,2	K562	blood:
8	chr19:18598368..18601612-chr19:18604293..18607199,5	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000006015	Chromatin interaction
ENSG00000105700	Chromatin interaction

Extended variants
information (count: 79 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:71)

rs_ID	r²[population]
rs10402322	0.80[AMR][1000 genomes];0.92[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10409346	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10409408	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10410797	0.86[AFR][1000 genomes];0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10413922	0.86[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs10416993	0.88[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10418331	0.82[AMR][1000 genomes];0.91[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10418554	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10420384	0.89[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10423802	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10426768	0.85[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1045631	0.89[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11086110	0.84[EUR][1000 genomes]
rs11668704	0.84[AMR][1000 genomes];0.90[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11670392	0.83[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11672385	0.83[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11879757	0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12980726	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12982295	0.84[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12983263	0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1469412	0.80[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1469413	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1971093	0.81[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2013069	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2303692	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs28534973	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2891676	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs34213500	0.84[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs35004712	0.82[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs35742476	0.80[AMR][1000 genomes];0.91[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4006662	0.80[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4303657	0.81[AFR][1000 genomes];0.89[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4580317	0.83[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4808135	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4808802	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4808803	0.83[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4808805	0.81[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4808806	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4808807	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4808808	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4808811	0.83[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4808812	0.81[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4808813	0.80[AMR][1000 genomes];0.92[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs55715336	0.80[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs57923655	0.80[AMR][1000 genomes];0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6512268	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6512269	0.84[AFR][1000 genomes];0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6512270	0.84[AFR][1000 genomes];0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6512271	0.80[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7246788	0.81[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7247540	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7249760	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7252130	0.80[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7252185	0.80[AMR][1000 genomes];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7255936	0.85[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7256530	0.88[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7258891	0.84[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7259135	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7507218	0.80[AMR][1000 genomes];0.93[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs8100343	0.85[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs8102717	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs8104247	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8106068	0.81[AFR][1000 genomes];0.89[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs8106332	0.80[AMR][1000 genomes];0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs8111397	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs8111582	0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs8111824	0.84[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs8112372	0.80[AMR][1000 genomes];0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs8112859	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs888668	0.91[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs888669	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes];0.93[ASN][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	esv3323899	chr19:18343484-18620429	Enhancers Weak transcription Strong transcription Active TSS ZNF genes & repeats Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	162 gene(s)	inside rSNPs	diseases
2	nsv911274	chr19:18440942-18691942	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	83 gene(s)	inside rSNPs	diseases
3	nsv1057795	chr19:18453362-18883844	Active TSS Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	92 gene(s)	inside rSNPs	diseases
4	nsv543925	chr19:18453362-18883844	Weak transcription Genic enhancers Strong transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	92 gene(s)	inside rSNPs	diseases
5	nsv428018	chr19:18454891-18663981	Enhancers Genic enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	61 gene(s)	inside rSNPs	diseases
6	nsv1060687	chr19:18522527-18643218	Genic enhancers Strong transcription Flanking Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	54 gene(s)	inside rSNPs	diseases
7	nsv532615	chr19:18534867-18796031	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	71 gene(s)	inside rSNPs	diseases
8	nsv1061733	chr19:18574940-18679155	Weak transcription Genic enhancers Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	32 gene(s)	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs2162797	LOC646044///SSBP4	Cis_1M	lymphoblastoid	RTeQTL
rs2162797	SSBP4	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:109 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:18575400-18607200	Weak transcription	Pancreatic Islets	Pancreatic Islet
2	chr19:18591000-18605400	Weak transcription	Thymus	Thymus
3	chr19:18591400-18605200	Weak transcription	Primary T cells from cord blood	blood
4	chr19:18591400-18605400	Weak transcription	GM12878-XiMat	blood
5	chr19:18593600-18606400	Enhancers	Primary T cells fromperipheralblood	blood
6	chr19:18593800-18601600	Enhancers	Liver	Liver
7	chr19:18594000-18601800	Enhancers	Lung	lung
8	chr19:18594000-18605000	Enhancers	Pancreas	Pancrea
9	chr19:18594000-18621800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
10	chr19:18594200-18601600	Enhancers	Placenta	Placenta
11	chr19:18594600-18605600	Weak transcription	Fetal Brain Female	brain
12	chr19:18595400-18601800	Enhancers	Left Ventricle	heart
13	chr19:18595400-18605800	Enhancers	Primary neutrophils fromperipheralblood	blood
14	chr19:18595600-18601600	Enhancers	Psoas Muscle	Psoas
15	chr19:18595600-18601800	Enhancers	Right Ventricle	heart
16	chr19:18596000-18601200	Enhancers	Right Atrium	heart
17	chr19:18596000-18601400	Enhancers	Fetal Thymus	thymus
18	chr19:18596200-18601200	Enhancers	Brain Anterior Caudate	brain
19	chr19:18597200-18601800	Enhancers	Fetal Muscle Leg	muscle
20	chr19:18597400-18603800	Weak transcription	Fetal Kidney	kidney
21	chr19:18597600-18602000	Enhancers	K562	blood
22	chr19:18597600-18606600	Enhancers	Duodenum Mucosa	Duodenum
23	chr19:18597800-18603800	Weak transcription	Fetal Lung	lung
24	chr19:18597800-18604400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr19:18597800-18604400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
26	chr19:18597800-18605400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
27	chr19:18598000-18601200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
28	chr19:18598000-18603400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
29	chr19:18598000-18604400	Weak transcription	NHLF	lung
30	chr19:18598000-18605200	Weak transcription	Primary B cells from peripheral blood	blood
31	chr19:18598000-18609800	Weak transcription	Fetal Intestine Large	intestine
32	chr19:18598200-18605400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
33	chr19:18598400-18604200	Weak transcription	Small Intestine	intestine
34	chr19:18598600-18603800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
35	chr19:18598800-18605400	Weak transcription	Primary B cells from cord blood	blood
36	chr19:18599000-18602000	Enhancers	Primary T helper cells fromperipheralblood	blood
37	chr19:18599200-18601400	Enhancers	H1 Cell Line	embryonic stem cell
38	chr19:18599200-18604600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
39	chr19:18599400-18601800	Genic enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
40	chr19:18599400-18604000	Weak transcription	Sigmoid Colon	Sigmoid Colon
41	chr19:18599400-18611200	Weak transcription	Brain Germinal Matrix	brain
42	chr19:18599600-18601600	Weak transcription	Primary T helper cells PMA-I stimulated	--
43	chr19:18599600-18604600	Weak transcription	Osteobl	bone
44	chr19:18599600-18604800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
45	chr19:18599600-18605600	Weak transcription	Rectal Mucosa Donor 31	rectum
46	chr19:18599800-18604200	Weak transcription	Muscle Satellite Cultured Cells	--
47	chr19:18599800-18604400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
48	chr19:18599800-18604400	Weak transcription	Stomach Mucosa	stomach
49	chr19:18599800-18604800	Weak transcription	Primary monocytes fromperipheralblood	blood
50	chr19:18599800-18605200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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