Variant report

Variant	rs2024432
Chromosome Location	chr2:10731474-10731475
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr2:10730122..10732482-chr2:10737387..10739514,4	K562	blood:
2	chr2:10727806..10729662-chr2:10731147..10733924,2	K562	blood:
3	chr2:10724831..10728793-chr2:10731457..10735556,4	MCF-7	breast:
4	chr2:10723207..10725627-chr2:10730117..10731698,2	K562	blood:

Variant related genes	Relation type
ENSG00000234818	Chromatin interaction

Extended variants
information (count: 103 )
Associated
traits (count: 3 )

rSNPs within LD-proxies of this variant (count:97)

rs_ID	r²[population]
rs10084172	0.84[ASW][hapmap];0.92[CEU][hapmap];0.90[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.81[TSI][hapmap];0.93[AMR][1000 genomes];0.87[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10166765	0.91[ASN][1000 genomes]
rs10167779	0.90[ASN][1000 genomes]
rs10168351	0.93[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10168852	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10174605	0.91[ASN][1000 genomes]
rs10175555	0.91[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[ASN][1000 genomes]
rs10175884	0.89[ASN][1000 genomes]
rs10177062	0.88[ASN][1000 genomes]
rs10178587	0.91[AFR][1000 genomes]
rs10178751	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10179854	0.81[ASN][1000 genomes]
rs10182589	0.91[ASN][1000 genomes]
rs10183359	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10183883	0.94[AFR][1000 genomes];0.96[AMR][1000 genomes];0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10186984	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.80[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.91[MKK][hapmap];0.97[TSI][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10187659	0.87[ASN][1000 genomes]
rs10188373	0.89[ASN][1000 genomes]
rs10190673	0.89[ASN][1000 genomes]
rs10190774	0.89[ASN][1000 genomes]
rs10198971	0.89[ASN][1000 genomes]
rs10199635	0.83[ASN][1000 genomes]
rs10199831	0.91[ASN][1000 genomes]
rs10202370	0.90[ASN][1000 genomes]
rs10207885	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];0.96[MKK][hapmap];0.97[TSI][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10208103	0.91[ASN][1000 genomes]
rs10211190	0.91[ASN][1000 genomes]
rs10803724	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10803725	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10929676	0.85[LWK][hapmap];0.88[YRI][hapmap]
rs10929677	0.89[ASN][1000 genomes]
rs10929678	0.91[ASN][1000 genomes]
rs10929679	0.91[ASN][1000 genomes]
rs10929680	0.91[ASN][1000 genomes]
rs10929681	0.84[CHB][hapmap];0.91[ASN][1000 genomes]
rs10929683	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];1.00[MKK][hapmap];0.97[TSI][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10929684	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];1.00[MKK][hapmap];0.97[TSI][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10929685	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];1.00[MKK][hapmap];0.97[TSI][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11680664	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11684537	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];1.00[MKK][hapmap];0.97[TSI][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12104950	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12329184	0.91[ASN][1000 genomes]
rs12473787	0.87[ASN][1000 genomes]
rs12473957	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];1.00[MKK][hapmap];0.97[TSI][hapmap];1.00[YRI][hapmap];0.89[ASN][1000 genomes]
rs12474625	0.83[JPT][hapmap]
rs12475662	0.88[ASN][1000 genomes]
rs12476554	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.97[GIH][hapmap];0.94[JPT][hapmap];1.00[LWK][hapmap];0.94[MKK][hapmap];0.97[TSI][hapmap];0.91[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12613769	0.90[CHB][hapmap];0.94[JPT][hapmap];0.91[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12618726	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12621977	0.91[ASN][1000 genomes]
rs12622053	0.91[ASN][1000 genomes]
rs12690510	0.94[AFR][1000 genomes];0.97[AMR][1000 genomes];0.89[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12692412	0.84[ASW][hapmap];0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.89[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.81[TSI][hapmap];0.91[ASN][1000 genomes]
rs12692414	0.94[AFR][1000 genomes];0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12692420	0.88[CEU][hapmap];0.90[CHB][hapmap];1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs12995465	0.89[ASN][1000 genomes]
rs12996735	0.89[ASN][1000 genomes]
rs13009015	0.91[AMR][1000 genomes];0.88[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs13027316	0.90[ASN][1000 genomes]
rs13407040	0.85[CEU][hapmap];0.90[CHB][hapmap];1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs13424648	0.87[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs13425171	0.93[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13427815	0.86[ASN][1000 genomes]
rs13430911	0.93[AMR][1000 genomes];0.88[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1861299	0.92[CEU][hapmap];0.90[CHB][hapmap];1.00[JPT][hapmap];0.93[AMR][1000 genomes];0.89[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1861300	0.92[CEU][hapmap];0.88[CHB][hapmap];1.00[JPT][hapmap];0.93[AMR][1000 genomes];0.89[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2024433	0.97[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2160258	0.89[ASN][1000 genomes]
rs2357649	0.81[JPT][hapmap]
rs2357650	0.81[JPT][hapmap]
rs2884232	0.89[ASN][1000 genomes]
rs34595606	0.91[ASN][1000 genomes]
rs35859525	0.90[ASN][1000 genomes]
rs55750243	0.91[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62127189	0.93[AMR][1000 genomes];0.89[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs62127197	0.88[ASN][1000 genomes]
rs62128635	0.91[ASN][1000 genomes]
rs6711473	0.91[ASN][1000 genomes]
rs6714787	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6717431	0.91[ASN][1000 genomes]
rs6720112	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.91[ASN][1000 genomes]
rs6721857	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];1.00[MKK][hapmap];0.97[TSI][hapmap];1.00[YRI][hapmap];0.91[ASN][1000 genomes]
rs6722126	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];1.00[MKK][hapmap];0.97[TSI][hapmap];0.96[YRI][hapmap];0.91[ASN][1000 genomes]
rs6730247	0.91[ASN][1000 genomes]
rs6732429	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.90[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.86[MKK][hapmap];0.95[TSI][hapmap];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6740245	1.00[CEU][hapmap];0.90[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6751436	0.91[ASN][1000 genomes]
rs6755281	0.93[AMR][1000 genomes];0.88[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs744809	0.85[CEU][hapmap];0.90[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.85[ASN][1000 genomes]
rs7572489	1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7589694	0.88[ASN][1000 genomes]
rs759401	0.87[ASN][1000 genomes]
rs7598541	0.88[ASN][1000 genomes]
rs9287718	0.84[ASW][hapmap];0.92[CEU][hapmap];0.89[CHB][hapmap];1.00[CHD][hapmap];0.87[GIH][hapmap];1.00[JPT][hapmap];0.93[MEX][hapmap];0.81[TSI][hapmap];0.88[ASN][1000 genomes]
rs9287721	1.00[CHD][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.88[ASN][1000 genomes]
rs9973374	0.89[ASN][1000 genomes]
rs9973456	0.89[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1007185	chr2:10540386-10791743	Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	52 gene(s)	inside rSNPs	diseases
2	nsv833370	chr2:10625149-10785402	Enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
3	nsv1009897	chr2:10627248-10751468	Enhancers Strong transcription Bivalent Enhancer Genic enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
4	nsv1000953	chr2:10717304-10921805	Strong transcription Enhancers Active TSS Bivalent Enhancer Genic enhancers Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
5	nsv535584	chr2:10717304-10921805	Bivalent Enhancer Weak transcription Strong transcription Enhancers Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
6	nsv833381	chr2:10723465-10911284	Strong transcription Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Genic enhancers Enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases

mRNA abundance (count:3)

SNP	Gene	Cis/trans	Tissue	Source
rs2024432	PDIA6	cis	cerebellum	SCAN
rs2024432	CYS1	cis	lymphoblastoid	seeQTL
rs2024432	NOL10	cis	parietal	SCAN

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:10698600-10736600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr2:10705800-10736000	Strong transcription	Duodenum Mucosa	Duodenum
3	chr2:10708600-10732000	Strong transcription	Monocytes-CD14+_RO01746	blood
4	chr2:10708800-10732800	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
5	chr2:10709200-10746800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr2:10709400-10732600	Strong transcription	Primary B cells from cord blood	blood
7	chr2:10712600-10742000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
8	chr2:10717600-10732400	Weak transcription	Fetal Brain Male	brain
9	chr2:10718000-10732000	Weak transcription	Brain Cingulate Gyrus	brain
10	chr2:10719800-10746600	Strong transcription	Primary hematopoietic stem cells short term culture	blood
11	chr2:10720000-10746400	Strong transcription	Dnd41	blood
12	chr2:10720400-10740200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
13	chr2:10720800-10739200	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
14	chr2:10721000-10755000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
15	chr2:10721200-10734600	Strong transcription	GM12878-XiMat	blood
16	chr2:10721200-10746800	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
17	chr2:10721400-10735800	Strong transcription	Primary T cells from cord blood	blood
18	chr2:10721600-10731800	Strong transcription	iPS-20b Cell Line	embryonic stem cell
19	chr2:10721600-10735600	Strong transcription	Primary T helper cells PMA-I stimulated	--
20	chr2:10722000-10735200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
21	chr2:10722000-10738200	Strong transcription	Fetal Muscle Leg	muscle
22	chr2:10722400-10734800	Strong transcription	Primary T cells fromperipheralblood	blood
23	chr2:10722400-10735200	Strong transcription	Primary T helper cells fromperipheralblood	blood
24	chr2:10722800-10732400	Strong transcription	Fetal Thymus	thymus
25	chr2:10722800-10741400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr2:10724000-10735600	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
27	chr2:10725600-10744000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr2:10725600-10758800	Weak transcription	Stomach Mucosa	stomach
29	chr2:10725600-10793400	Weak transcription	Pancreatic Islets	Pancreatic Islet
30	chr2:10725800-10787000	Weak transcription	Fetal Heart	heart
31	chr2:10726000-10732400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
32	chr2:10726000-10738400	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
33	chr2:10726000-10746200	Weak transcription	Placenta Amnion	Placenta Amnion
34	chr2:10726000-10747600	Strong transcription	HepG2	liver
35	chr2:10726200-10732800	Strong transcription	Fetal Stomach	stomach
36	chr2:10727200-10733000	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
37	chr2:10727400-10732600	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chr2:10727400-10736200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
39	chr2:10727600-10732600	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
40	chr2:10727600-10732600	Strong transcription	Fetal Muscle Trunk	muscle
41	chr2:10727600-10732600	Strong transcription	Thymus	Thymus
42	chr2:10727600-10734600	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
43	chr2:10727600-10737000	Strong transcription	Fetal Intestine Small	intestine
44	chr2:10727600-10739400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
45	chr2:10727800-10731600	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
46	chr2:10727800-10732400	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
47	chr2:10727800-10732400	Strong transcription	Skeletal Muscle Female	skeletal muscle
48	chr2:10727800-10732600	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
49	chr2:10727800-10732600	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
50	chr2:10727800-10732600	Strong transcription	Skeletal Muscle Male	skeletal muscle

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