Variant report

Variant	rs12532454
Chromosome Location	chr7:26387731-26387732
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr7:26386222..26388194-chr7:26390840..26392963,3	MCF-7	breast:
2	chr7:26240262..26243244-chr7:26384656..26387797,3	MCF-7	breast:
3	chr7:26382800..26384799-chr7:26387254..26389366,2	K562	blood:
4	chr7:26238981..26240863-chr7:26385040..26387955,2	MCF-7	breast:
5	chr7:26385066..26388736-chr7:26388870..26392528,4	K562	blood:

Variant related genes	Relation type
ENSG00000122566	Chromatin interaction
ENSG00000122565	Chromatin interaction

Extended variants
information (count: 51 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:47)

rs_ID	r²[population]
rs10230728	0.87[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[YRI][hapmap];0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];0.91[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10231242	0.81[ASN][1000 genomes]
rs10231349	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10235391	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10238493	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][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]
rs10238702	0.95[JPT][hapmap]
rs10238717	0.81[ASN][1000 genomes]
rs10246401	0.90[CEU][hapmap];0.82[CHB][hapmap];0.96[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10252532	0.87[CEU][hapmap];0.91[CHB][hapmap];1.00[JPT][hapmap];0.85[AMR][1000 genomes];0.87[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10254065	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10260489	0.81[ASN][1000 genomes]
rs10267867	0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10270099	0.91[CEU][hapmap];0.81[CHB][hapmap];0.95[JPT][hapmap];0.84[AMR][1000 genomes];0.87[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10270279	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10281957	0.80[ASN][1000 genomes]
rs10951130	0.91[JPT][hapmap];0.83[ASN][1000 genomes]
rs12532077	0.91[JPT][hapmap];0.81[ASN][1000 genomes]
rs12532473	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12534816	0.91[JPT][hapmap];0.83[ASN][1000 genomes]
rs12535203	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[YRI][hapmap];0.98[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12537520	0.83[ASN][1000 genomes]
rs12537599	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][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]
rs12666571	0.81[ASN][1000 genomes]
rs12669655	0.81[ASN][1000 genomes]
rs13243295	0.81[ASN][1000 genomes]
rs13243466	0.81[ASN][1000 genomes]
rs13244200	0.91[JPT][hapmap];0.81[ASN][1000 genomes]
rs17153471	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][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]
rs17153475	0.91[CEU][hapmap];0.81[EUR][1000 genomes]
rs1852860	0.91[JPT][hapmap];0.81[ASN][1000 genomes]
rs2014729	0.95[JPT][hapmap];0.81[ASN][1000 genomes]
rs2014735	0.91[JPT][hapmap];0.81[ASN][1000 genomes]
rs2391270	0.87[CEU][hapmap];0.87[CHB][hapmap];0.95[JPT][hapmap];0.82[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2391276	0.92[CEU][hapmap];0.96[CHB][hapmap];1.00[JPT][hapmap];0.88[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs35042524	0.80[ASN][1000 genomes]
rs35749074	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3757664	0.94[AMR][1000 genomes];0.91[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs3757665	0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs3757666	1.00[CHB][hapmap];0.91[JPT][hapmap];0.89[AMR][1000 genomes];0.81[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs3801888	0.91[CEU][hapmap];0.81[EUR][1000 genomes]
rs3801890	0.91[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.87[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs3801891	0.95[CEU][hapmap];0.96[CHB][hapmap];1.00[JPT][hapmap];0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs3823943	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4506105	0.91[CEU][hapmap];0.91[CHB][hapmap];0.95[JPT][hapmap];0.84[AMR][1000 genomes];0.86[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs61558019	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6947348	0.83[ASN][1000 genomes]
rs7784736	0.81[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1021308	chr7:26116605-26419720	Weak transcription Active TSS Enhancers Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	166 gene(s)	inside rSNPs	diseases
2	nsv1029596	chr7:26302739-26737913	Flanking Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
3	nsv538804	chr7:26302739-26737913	Strong transcription Weak transcription Flanking Active TSS Enhancers Genic enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
4	esv2761313	chr7:26340970-26389772	Enhancers Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs12532454	SNX10	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:60 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:26368800-26405000	Weak transcription	Placenta	Placenta
2	chr7:26372400-26405200	Weak transcription	Primary T helper cells PMA-I stimulated	--
3	chr7:26375000-26414000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
4	chr7:26382600-26388000	Strong transcription	Primary monocytes fromperipheralblood	blood
5	chr7:26382600-26392000	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
6	chr7:26382600-26393400	Strong transcription	Primary neutrophils fromperipheralblood	blood
7	chr7:26382800-26392800	Strong transcription	Primary B cells from cord blood	blood
8	chr7:26384000-26389400	Weak transcription	Sigmoid Colon	Sigmoid Colon
9	chr7:26384600-26389000	Enhancers	HepG2	liver
10	chr7:26384600-26391200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
11	chr7:26384600-26393000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
12	chr7:26384800-26388600	Strong transcription	Fetal Thymus	thymus
13	chr7:26384800-26409400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
14	chr7:26385000-26388200	Weak transcription	Fetal Brain Female	brain
15	chr7:26385000-26388800	Strong transcription	Primary T cells fromperipheralblood	blood
16	chr7:26385000-26389600	Weak transcription	Brain Inferior Temporal Lobe	brain
17	chr7:26385200-26390200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
18	chr7:26385200-26391200	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
19	chr7:26385200-26393000	Strong transcription	Primary B cells from peripheral blood	blood
20	chr7:26385600-26389000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
21	chr7:26385600-26390000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
22	chr7:26385600-26414200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
23	chr7:26385800-26388200	Strong transcription	Dnd41	blood
24	chr7:26385800-26388600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
25	chr7:26386000-26390000	Strong transcription	Primary hematopoietic stem cells	blood
26	chr7:26386000-26390200	Strong transcription	Primary T cells from cord blood	blood
27	chr7:26386200-26387800	Genic enhancers	GM12878-XiMat	blood
28	chr7:26386200-26388000	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
29	chr7:26386200-26388200	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
30	chr7:26386200-26388200	Strong transcription	Primary T helper cells fromperipheralblood	blood
31	chr7:26386200-26388200	Strong transcription	Spleen	Spleen
32	chr7:26386400-26387800	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
33	chr7:26386400-26391800	Weak transcription	K562	blood
34	chr7:26386600-26387800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
35	chr7:26386600-26405200	Weak transcription	Thymus	Thymus
36	chr7:26386800-26387800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
37	chr7:26386800-26387800	Strong transcription	Monocytes-CD14+_RO01746	blood
38	chr7:26386800-26388000	Weak transcription	Adipose Nuclei	Adipose
39	chr7:26386800-26388000	Weak transcription	Lung	lung
40	chr7:26386800-26393200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
41	chr7:26386800-26395600	Weak transcription	Fetal Lung	lung
42	chr7:26387000-26388000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
43	chr7:26387000-26388200	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
44	chr7:26387000-26388400	Genic enhancers	Primary hematopoietic stem cells short term culture	blood
45	chr7:26387000-26390200	Enhancers	Fetal Intestine Large	intestine
46	chr7:26387200-26387800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
47	chr7:26387200-26388200	Weak transcription	NHEK	skin
48	chr7:26387200-26388400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
49	chr7:26387200-26388600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
50	chr7:26387200-26388600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links