Variant report

Variant	rs1061986
Chromosome Location	chr12:48736439-48736440
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr12:48735709..48737484-chr12:48748152..48750019,2	MCF-7	breast:
2	chr12:48731724..48737573-chr12:48737990..48746470,14	K562	blood:
3	chr12:48732421..48734160-chr12:48734497..48737400,2	MCF-7	breast:
4	chr12:48732035..48733570-chr12:48734227..48737131,2	MCF-7	breast:
5	chr12:48727374..48736715-chr12:48738720..48747602,13	K562	blood:

Variant related genes	Relation type
ENSG00000167528	Chromatin interaction
ENSG00000257735	Chromatin interaction

Extended variants
information (count: 65 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:54)

rs_ID	r²[population]
rs1107654	0.94[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs11168468	0.82[EUR][1000 genomes]
rs11168474	0.81[EUR][1000 genomes]
rs11168484	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs12828309	0.89[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs12829841	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs1387259	0.86[AFR][1000 genomes];0.97[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs1387260	0.86[AFR][1000 genomes];0.97[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs1489108	0.95[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs1542707	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs1552550	0.89[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs1601985	0.87[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs2054905	0.94[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs2409003	0.88[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs2409004	0.88[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs2450994	0.88[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs2450996	0.83[EUR][1000 genomes]
rs2468943	0.92[EUR][1000 genomes]
rs2468949	0.81[EUR][1000 genomes]
rs2634670	0.88[AMR][1000 genomes];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2634676	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2634678	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2634680	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2634681	0.82[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs2634682	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs2634684	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2634686	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs2634688	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs2634689	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs2634691	0.86[AFR][1000 genomes];0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2634692	0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2634693	0.86[AFR][1000 genomes];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2634694	0.86[AFR][1000 genomes];0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2732441	0.82[AFR][1000 genomes];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs2732445	0.81[AMR][1000 genomes]
rs2732448	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs2732453	0.82[AFR][1000 genomes];0.95[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs2732454	0.86[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs2732457	0.98[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2732461	0.92[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs2732462	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2732466	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2732479	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2732481	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2732484	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2732486	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2732488	0.87[AMR][1000 genomes];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2956703	0.94[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs2956710	0.87[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs34286639	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs6580662	0.82[EUR][1000 genomes]
rs7960122	0.82[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs7966829	0.81[EUR][1000 genomes]
rs923397	0.88[AMR][1000 genomes];0.95[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2758307	chr12:48429702-48825499	Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	57 gene(s)	inside rSNPs	diseases
2	esv2759898	chr12:48429702-48825499	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	57 gene(s)	inside rSNPs	diseases
3	nsv8971	chr12:48536526-48758501	Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Strong transcription Bivalent/Poised TSS Genic enhancers Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
4	esv34439	chr12:48541757-48779562	Bivalent/Poised TSS Flanking Active TSS Weak transcription Active TSS Enhancers Strong transcription Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	39 gene(s)	inside rSNPs	diseases
5	esv2757502	chr12:48547128-48779562	Genic enhancers Flanking Active TSS Enhancers Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	39 gene(s)	inside rSNPs	diseases
6	nsv427911	chr12:48670336-48979396	Weak transcription Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Enhancers Bivalent Enhancer ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	35 gene(s)	inside rSNPs	diseases
7	nsv832402	chr12:48686761-48851020	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
8	nsv826362	chr12:48693048-48768853	Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
9	nsv437752	chr12:48721832-48741219	Weak transcription Strong transcription Enhancers Genic enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Active TSS	TF binding region CpG island Chromatin interactive region	10 gene(s)	inside rSNPs	diseases
10	nsv1044444	chr12:48725007-48737570	Strong transcription Enhancers Weak transcription Genic enhancers Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	7 gene(s)	inside rSNPs	n/a
11	nsv1045159	chr12:48730024-48748940	Weak transcription Bivalent/Poised TSS Strong transcription Flanking Active TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs1061986	H1FNT	cis	Muscle Skeletal	GTEx
rs1061986	H1FNT	cis	Artery Tibial	GTEx

Chromatin state (count:119 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:48723800-48736600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr12:48725200-48736800	Weak transcription	Hela-S3	cervix
3	chr12:48728800-48736600	Weak transcription	Right Ventricle	heart
4	chr12:48728800-48737000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
5	chr12:48729000-48739200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
6	chr12:48729200-48736600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
7	chr12:48729200-48736600	Weak transcription	Fetal Intestine Small	intestine
8	chr12:48729200-48736600	Weak transcription	Pancreas	Pancrea
9	chr12:48729200-48743400	Weak transcription	Stomach Mucosa	stomach
10	chr12:48730200-48736600	Weak transcription	Ovary	ovary
11	chr12:48730600-48736800	Weak transcription	Pancreatic Islets	Pancreatic Islet
12	chr12:48731200-48738200	Weak transcription	Primary hematopoietic stem cells	blood
13	chr12:48731200-48743800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
14	chr12:48731400-48736800	Weak transcription	Psoas Muscle	Psoas
15	chr12:48732000-48736600	Weak transcription	Gastric	stomach
16	chr12:48732000-48736600	Weak transcription	Rectal Smooth Muscle	rectum
17	chr12:48732400-48736800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
18	chr12:48732400-48742600	Strong transcription	Left Ventricle	heart
19	chr12:48732600-48736600	Weak transcription	Osteobl	bone
20	chr12:48732600-48736800	Weak transcription	GM12878-XiMat	blood
21	chr12:48732600-48738000	Weak transcription	Small Intestine	intestine
22	chr12:48732600-48742600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
23	chr12:48732800-48736600	Strong transcription	Primary T cells fromperipheralblood	blood
24	chr12:48732800-48736600	Weak transcription	Esophagus	oesophagus
25	chr12:48732800-48737000	Weak transcription	NH-A	brain
26	chr12:48733200-48742000	Strong transcription	Brain Hippocampus Middle	brain
27	chr12:48733200-48742200	Strong transcription	Fetal Thymus	thymus
28	chr12:48733400-48739600	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
29	chr12:48733400-48741000	Strong transcription	Primary T helper cells PMA-I stimulated	--
30	chr12:48733600-48736600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
31	chr12:48733600-48737400	Weak transcription	HepG2	liver
32	chr12:48733600-48742000	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
33	chr12:48733600-48742200	Strong transcription	Primary B cells from cord blood	blood
34	chr12:48733600-48743800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
35	chr12:48733800-48742000	Strong transcription	Liver	Liver
36	chr12:48733800-48742200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr12:48733800-48742800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
38	chr12:48734000-48736800	Weak transcription	Muscle Satellite Cultured Cells	--
39	chr12:48734000-48736800	Weak transcription	NHEK	skin
40	chr12:48734000-48741800	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
41	chr12:48734000-48741800	Strong transcription	Fetal Brain Female	brain
42	chr12:48734000-48742000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
43	chr12:48734000-48742200	Strong transcription	Primary B cells from peripheral blood	blood
44	chr12:48734000-48742600	Strong transcription	Fetal Muscle Leg	muscle
45	chr12:48734200-48742000	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
46	chr12:48734600-48736600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
47	chr12:48734600-48736600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
48	chr12:48734600-48736600	Weak transcription	NHLF	lung
49	chr12:48734600-48737000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
50	chr12:48734600-48739000	Weak transcription	A549	lung

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links