Variant report

Variant	rs903119
Chromosome Location	chr1:212434241-212434242
allele	A/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	chr1:212433580..212437066-chr1:212438671..212444004,6	K562	blood:
2	chr1:212428170..212430153-chr1:212432529..212434264,2	K562	blood:
3	chr1:212433329..212435940-chr1:212436148..212437997,2	K562	blood:
4	chr1:212432994..212436361-chr1:212456253..212459634,4	K562	blood:
5	chr1:212432987..212434829-chr1:212436497..212438053,2	K562	blood:
6	chr1:211770787..211772402-chr1:212434054..212436587,2	K562	blood:
7	chr1:212427899..212432292-chr1:212432529..212438731,7	K562	blood:
8	chr1:212432823..212434470-chr1:212457491..212460083,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000066027	Chromatin interaction

Extended variants
information (count: 57 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:52)

rs_ID	r²[population]
rs1011232	0.82[CHB][hapmap];0.95[JPT][hapmap];0.97[ASN][1000 genomes]
rs1056985	1.00[CEU][hapmap]
rs10735509	0.82[CHB][hapmap];0.95[JPT][hapmap];0.97[ASN][1000 genomes]
rs10779577	0.97[ASN][1000 genomes]
rs10863955	0.93[CEU][hapmap]
rs10863956	1.00[AFR][1000 genomes];0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10863957	0.86[CHB][hapmap];0.94[JPT][hapmap];0.94[ASN][1000 genomes]
rs10863958	0.82[CHB][hapmap];0.95[JPT][hapmap];0.97[ASN][1000 genomes]
rs10863965	1.00[CEU][hapmap]
rs11119886	1.00[ASW][hapmap];0.93[CEU][hapmap];0.90[TSI][hapmap];1.00[AFR][1000 genomes]
rs11119888	0.90[CHB][hapmap];0.94[JPT][hapmap];0.97[ASN][1000 genomes]
rs11119890	0.91[CHB][hapmap];0.95[JPT][hapmap];0.98[ASN][1000 genomes]
rs11119891	1.00[CEU][hapmap];0.91[CHB][hapmap];0.95[JPT][hapmap];1.00[AFR][1000 genomes];0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11119893	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11119903	0.85[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs11119907	1.00[AFR][1000 genomes]
rs11119908	1.00[AFR][1000 genomes]
rs11119910	0.91[CEU][hapmap];1.00[AFR][1000 genomes]
rs11119932	1.00[CEU][hapmap]
rs11119934	0.93[CEU][hapmap]
rs12118709	1.00[AFR][1000 genomes]
rs12118732	1.00[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs12119183	0.92[ASN][1000 genomes]
rs12119779	1.00[CEU][hapmap]
rs12124582	1.00[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs12127954	0.95[JPT][hapmap];0.87[ASN][1000 genomes]
rs12128965	1.00[CEU][hapmap];0.85[CHB][hapmap];1.00[AFR][1000 genomes]
rs12129267	1.00[AFR][1000 genomes]
rs12133582	1.00[CEU][hapmap]
rs12134074	1.00[AFR][1000 genomes];0.85[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs12136095	1.00[CEU][hapmap];0.85[TSI][hapmap]
rs12137798	1.00[AFR][1000 genomes]
rs12141427	1.00[CEU][hapmap]
rs12143853	1.00[CEU][hapmap];1.00[AFR][1000 genomes]
rs12145377	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12145451	0.97[ASN][1000 genomes]
rs12145484	1.00[CEU][hapmap];0.85[TSI][hapmap]
rs12146141	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12403586	1.00[CEU][hapmap]
rs12561785	1.00[AFR][1000 genomes]
rs12562618	1.00[AFR][1000 genomes];0.85[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs1342152	1.00[CEU][hapmap];1.00[AFR][1000 genomes];0.85[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs14123	1.00[CEU][hapmap];0.85[TSI][hapmap]
rs1493601	1.00[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs17018777	0.93[CEU][hapmap]
rs17018847	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17018853	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2298115	0.86[CEU][hapmap];1.00[AFR][1000 genomes]
rs3820513	1.00[CEU][hapmap]
rs4951597	1.00[CEU][hapmap]
rs61260530	0.96[AMR][1000 genomes];0.91[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs884923	0.80[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv999738	chr1:212218618-212513690	Enhancers Weak transcription Strong transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
2	nsv1009376	chr1:212292357-212680320	Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	48 gene(s)	inside rSNPs	diseases
3	nsv549139	chr1:212332294-212876902	Flanking Active TSS Weak transcription Bivalent Enhancer Strong transcription Enhancers Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	114 gene(s)	inside rSNPs	diseases
4	nsv997629	chr1:212404489-212658785	Strong transcription Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	45 gene(s)	inside rSNPs	diseases
5	nsv535286	chr1:212404489-212658785	Strong transcription Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	45 gene(s)	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs903119	PPP2R5A	cis	Whole Blood	GTEx
rs903119	PPP2R5A	cis	Thyroid	GTEx

Chromatin state (count:43 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:212429200-212434400	Weak transcription	Sigmoid Colon	Sigmoid Colon
2	chr1:212429400-212434800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr1:212429400-212435600	Enhancers	Primary monocytes fromperipheralblood	blood
4	chr1:212430200-212434600	Weak transcription	Left Ventricle	heart
5	chr1:212430400-212435600	Enhancers	HepG2	liver
6	chr1:212430600-212435000	Enhancers	Adipose Nuclei	Adipose
7	chr1:212430800-212434400	Weak transcription	Right Atrium	heart
8	chr1:212430800-212434400	Weak transcription	Right Ventricle	heart
9	chr1:212431800-212434400	Weak transcription	Gastric	stomach
10	chr1:212433200-212435600	Enhancers	HMEC	breast
11	chr1:212433600-212435000	Enhancers	Breast Myoepithelial Primary Cells	Breast
12	chr1:212433600-212435200	Enhancers	Liver	Liver
13	chr1:212433600-212435400	Enhancers	Monocytes-CD14+_RO01746	blood
14	chr1:212433600-212435800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr1:212433800-212434400	Flanking Active TSS	NHEK	skin
16	chr1:212433800-212435000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
17	chr1:212433800-212435000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
18	chr1:212433800-212435200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
19	chr1:212433800-212435200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
20	chr1:212433800-212435600	Enhancers	Hela-S3	cervix
21	chr1:212434000-212434400	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
22	chr1:212434000-212434600	Enhancers	ES-I3 Cell Line	embryonic stem cell
23	chr1:212434000-212434600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
24	chr1:212434000-212434600	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
25	chr1:212434000-212434800	Weak transcription	Primary B cells from cord blood	blood
26	chr1:212434000-212434800	Enhancers	Primary T killer memory cells from peripheral blood	blood
27	chr1:212434000-212435000	Enhancers	iPS-20b Cell Line	embryonic stem cell
28	chr1:212434000-212435000	Enhancers	Pancreas	Pancrea
29	chr1:212434000-212435400	Enhancers	Primary T helper cells PMA-I stimulated	--
30	chr1:212434000-212435400	Enhancers	Stomach Mucosa	stomach
31	chr1:212434000-212435600	Enhancers	Fetal Intestine Small	intestine
32	chr1:212434000-212435800	Enhancers	Fetal Intestine Large	intestine
33	chr1:212434000-212435800	Enhancers	K562	blood
34	chr1:212434200-212434400	Enhancers	Thymus	Thymus
35	chr1:212434200-212434600	Enhancers	Primary hematopoietic stem cells short term culture	blood
36	chr1:212434200-212434600	Weak transcription	Esophagus	oesophagus
37	chr1:212434200-212434600	Weak transcription	Lung	lung
38	chr1:212434200-212435000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
39	chr1:212434200-212435000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
40	chr1:212434200-212435000	Enhancers	HUES48 Cell Line	embryonic stem cell
41	chr1:212434200-212435000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
42	chr1:212434200-212435200	Enhancers	Duodenum Mucosa	Duodenum
43	chr1:212434200-212435600	Enhancers	Primary T cells from cord blood	blood

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