Variant report

Variant	rs2910681
Chromosome Location	chr19:36713906-36713907
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr19:36711072..36713184-chr19:36713372..36715798,2	K562	blood:
2	chr19:36703714..36707271-chr19:36711666..36715110,4	MCF-7	breast:
3	chr19:36713025..36717797-chr19:36719610..36723880,4	K562	blood:

Variant related genes	Relation type
ENSG00000196357	Chromatin interaction
ENSG00000167635	Chromatin interaction

Extended variants
information (count: 58 )
Associated
traits (count: 3 )

rSNPs within LD-proxies of this variant (count:56)

rs_ID	r²[population]
rs10416729	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10418925	0.81[CEU][hapmap];0.91[CHB][hapmap]
rs11084857	0.86[CHB][hapmap];0.89[CHD][hapmap]
rs1127406	0.81[CHB][hapmap]
rs1129375	0.91[CHB][hapmap]
rs1129376	0.91[CHB][hapmap];0.92[CHD][hapmap];0.83[TSI][hapmap]
rs11673662	0.87[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs11882601	0.90[CHB][hapmap]
rs12460237	0.86[ASW][hapmap];1.00[CEU][hapmap];0.91[CHB][hapmap];0.95[GIH][hapmap];0.86[JPT][hapmap];0.97[LWK][hapmap];1.00[MEX][hapmap];0.84[MKK][hapmap];1.00[TSI][hapmap];0.96[YRI][hapmap];0.85[AFR][1000 genomes];0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs12608941	0.82[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs12609058	0.91[CHB][hapmap]
rs17639740	0.91[CHB][hapmap]
rs1898675	0.89[ASN][1000 genomes]
rs2432040	0.80[AFR][1000 genomes];0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2432044	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2432046	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2432048	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2432050	0.82[AFR][1000 genomes];0.87[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs2432053	1.00[ASW][hapmap];1.00[CHB][hapmap];0.97[CHD][hapmap];0.93[GIH][hapmap];1.00[JPT][hapmap];0.83[LWK][hapmap];0.92[MEX][hapmap];0.88[TSI][hapmap];1.00[YRI][hapmap];0.91[AFR][1000 genomes];0.87[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs2432055	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];0.93[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap]
rs2438515	0.91[AFR][1000 genomes];0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2438516	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2918322	0.93[ASN][1000 genomes]
rs2918323	0.83[ASN][1000 genomes]
rs2918324	0.95[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2918325	1.00[CHB][hapmap];0.89[GIH][hapmap];0.88[TSI][hapmap];0.84[ASN][1000 genomes]
rs2918376	0.91[AFR][1000 genomes];0.87[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs2918377	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2918381	0.85[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs2918383	0.90[ASN][1000 genomes]
rs2918384	1.00[CHB][hapmap];0.95[CHD][hapmap];0.93[GIH][hapmap];0.81[JPT][hapmap];0.88[MEX][hapmap];0.88[TSI][hapmap];0.93[ASN][1000 genomes]
rs2967490	0.91[CHB][hapmap];0.92[CHD][hapmap];0.83[TSI][hapmap]
rs2967491	0.91[CHB][hapmap];0.92[CHD][hapmap];0.83[TSI][hapmap]
rs2972320	0.93[ASN][1000 genomes]
rs2972528	0.94[EUR][1000 genomes]
rs2972530	0.81[ASN][1000 genomes]
rs2972532	0.95[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2972533	1.00[CHB][hapmap];0.92[CHD][hapmap];0.93[GIH][hapmap];0.81[JPT][hapmap];0.84[MEX][hapmap];0.88[TSI][hapmap];0.93[ASN][1000 genomes]
rs2972534	0.92[ASN][1000 genomes]
rs2972535	0.84[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs2972536	0.81[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs2972540	0.93[ASW][hapmap];0.91[CHB][hapmap];1.00[CHD][hapmap];0.91[GIH][hapmap];1.00[JPT][hapmap];0.88[TSI][hapmap];0.95[YRI][hapmap];0.80[AFR][1000 genomes];0.86[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs2972543	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2972630	0.91[CHB][hapmap]
rs2972631	0.81[CEU][hapmap];0.90[CHB][hapmap]
rs2972643	0.91[CHB][hapmap]
rs2972654	0.91[CHB][hapmap]
rs2972655	0.91[CHB][hapmap]
rs34912665	0.85[AFR][1000 genomes];0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4293497	0.84[AFR][1000 genomes];0.99[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4315447	0.98[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs57614488	0.89[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs60277419	0.82[AFR][1000 genomes];0.82[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs6510528	0.96[CEU][hapmap];0.86[CHB][hapmap];0.81[CHD][hapmap];0.95[GIH][hapmap];0.90[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.84[AMR][1000 genomes];0.95[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs8107260	0.94[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs8107616	0.83[AMR][1000 genomes];0.95[EUR][1000 genomes];0.84[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3526489	chr19:36306483-36741945	Enhancers Weak transcription Strong transcription Flanking Active TSS Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	114 gene(s)	inside rSNPs	diseases
2	esv3526490	chr19:36306483-36741945	Genic enhancers Weak transcription Strong transcription Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	114 gene(s)	inside rSNPs	diseases

mRNA abundance (count:3)

SNP	Gene	Cis/trans	Tissue	Source
rs2910681	ZNF545	Cis_1M	lymphoblastoid	RTeQTL
rs2910681	SHKBP1	cis	cerebellum	SCAN
rs2910681	ZNF234	cis	parietal	SCAN

Chromatin state (count:125 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:36706800-36716400	Weak transcription	Aorta	Aorta
2	chr19:36707000-36716200	Weak transcription	Rectal Smooth Muscle	rectum
3	chr19:36707000-36726800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
4	chr19:36707400-36730200	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr19:36707600-36731800	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr19:36707800-36716400	Weak transcription	Right Ventricle	heart
7	chr19:36707800-36717000	Weak transcription	HSMMtube	muscle
8	chr19:36708000-36714000	Genic enhancers	Dnd41	blood
9	chr19:36708000-36715000	Weak transcription	NHLF	lung
10	chr19:36708000-36716400	Weak transcription	Psoas Muscle	Psoas
11	chr19:36708000-36716800	Weak transcription	Pancreas	Pancrea
12	chr19:36708000-36719800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr19:36708200-36715000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
14	chr19:36708200-36730800	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Female	--
15	chr19:36708400-36715400	Weak transcription	Fetal Heart	heart
16	chr19:36708400-36716400	Weak transcription	Spleen	Spleen
17	chr19:36709000-36715400	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
18	chr19:36709000-36723000	Strong transcription	HUES48 Cell Line	embryonic stem cell
19	chr19:36709000-36723800	Strong transcription	HUES64 Cell Line	embryonic stem cell
20	chr19:36709000-36724000	Strong transcription	H1 Cell Line	embryonic stem cell
21	chr19:36709200-36716000	Strong transcription	HUES6 Cell Line	embryonic stem cell
22	chr19:36709200-36716000	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
23	chr19:36709400-36715200	Strong transcription	Fetal Lung	lung
24	chr19:36709400-36723800	Strong transcription	Fetal Muscle Trunk	muscle
25	chr19:36709800-36714000	Strong transcription	Placenta	Placenta
26	chr19:36710000-36714000	ZNF genes & repeats	Primary T regulatory cells fromperipheralblood	blood
27	chr19:36710000-36714000	Strong transcription	Osteobl	bone
28	chr19:36710000-36715000	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr19:36710000-36715000	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
30	chr19:36710000-36715200	ZNF genes & repeats	H9 Derived Neuron Cultured Cells	ES cell derived
31	chr19:36710000-36716000	Strong transcription	Primary B cells from peripheral blood	blood
32	chr19:36710000-36725000	ZNF genes & repeats	GM12878-XiMat	blood
33	chr19:36710000-36732200	ZNF genes & repeats	A549	lung
34	chr19:36710000-36732200	ZNF genes & repeats	Monocytes-CD14+_RO01746	blood
35	chr19:36710200-36720600	Strong transcription	Fetal Thymus	thymus
36	chr19:36710400-36714000	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
37	chr19:36710400-36714400	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
38	chr19:36710400-36715400	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
39	chr19:36710800-36714400	Strong transcription	Adipose Nuclei	Adipose
40	chr19:36710800-36719000	Weak transcription	Fetal Brain Male	brain
41	chr19:36710800-36719400	Weak transcription	Pancreatic Islets	Pancreatic Islet
42	chr19:36710800-36721800	ZNF genes & repeats	Primary neutrophils fromperipheralblood	blood
43	chr19:36710800-36723200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr19:36711000-36714000	Strong transcription	Hela-S3	cervix
45	chr19:36711000-36714000	Strong transcription	HMEC	breast
46	chr19:36711000-36714600	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
47	chr19:36711000-36715000	Strong transcription	Primary T helper cells PMA-I stimulated	--
48	chr19:36711000-36723200	Strong transcription	iPS-18 Cell Line	embryonic stem cell
49	chr19:36711000-36723400	Strong transcription	iPS-20b Cell Line	embryonic stem cell
50	chr19:36711000-36724000	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell

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