Variant report

Variant	rs61938827
Chromosome Location	chr12:105445798-105445799
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr12:105378818..105380572-chr12:105444808..105446443,2	K562	blood:
2	chr12:105435675..105437958-chr12:105444796..105446919,2	K562	blood:

Variant related genes	Relation type
ENSG00000151131	Chromatin interaction

Extended variants
information (count: 40 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:37)

rs_ID	r²[population]
rs10778366	0.94[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs10861327	0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs10861328	0.97[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs10861329	0.97[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs10861330	0.92[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs10861331	0.94[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs10861332	0.94[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs10861333	0.94[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs10861335	0.94[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs10861336	0.94[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs11112347	0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs11112349	0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs11112350	0.94[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs11112351	0.93[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs11112352	0.94[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs11112356	0.94[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs11611105	0.85[ASN][1000 genomes]
rs11612252	0.94[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs11613233	0.91[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs11613261	0.94[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs1196879	0.84[EUR][1000 genomes]
rs1196882	0.83[EUR][1000 genomes]
rs12367626	0.94[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs12581638	0.94[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs17242777	0.94[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs1732377	0.81[EUR][1000 genomes]
rs2374451	0.89[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs2440693	0.81[EUR][1000 genomes]
rs4144467	0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs4144468	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs56118650	0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs56188643	0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs56369757	0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7308195	0.94[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs7311691	0.94[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs73179949	0.94[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs7962686	0.90[AMR][1000 genomes];0.87[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv899495	chr12:104990469-105527011	Weak transcription Flanking Active TSS Enhancers Strong transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
2	nsv899498	chr12:105173598-105461620	Flanking Active TSS Weak transcription Enhancers Strong transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	22 gene(s)	inside rSNPs	diseases
3	nsv832505	chr12:105315352-105497765	Weak transcription Active TSS Strong transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:69 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:105409200-105446800	Weak transcription	Left Ventricle	heart
2	chr12:105409400-105465200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
3	chr12:105410800-105446400	Weak transcription	K562	blood
4	chr12:105413000-105476800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
5	chr12:105413200-105457800	Weak transcription	Duodenum Mucosa	Duodenum
6	chr12:105414800-105447200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
7	chr12:105414800-105454000	Weak transcription	HUES48 Cell Line	embryonic stem cell
8	chr12:105420000-105477000	Weak transcription	Skeletal Muscle Female	skeletal muscle
9	chr12:105420400-105448600	Weak transcription	Ovary	ovary
10	chr12:105420600-105447000	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
11	chr12:105423200-105459400	Weak transcription	Lung	lung
12	chr12:105431000-105446800	Weak transcription	Colon Smooth Muscle	Colon
13	chr12:105431400-105461600	Weak transcription	Rectal Mucosa Donor 29	rectum
14	chr12:105431800-105454800	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr12:105432200-105454600	Weak transcription	NHEK	skin
16	chr12:105434000-105453000	Weak transcription	Skeletal Muscle Male	skeletal muscle
17	chr12:105435200-105453600	Weak transcription	Fetal Stomach	stomach
18	chr12:105435600-105446200	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr12:105435600-105467400	Weak transcription	Brain Substantia Nigra	brain
20	chr12:105435800-105446600	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
21	chr12:105436800-105446600	Strong transcription	Osteobl	bone
22	chr12:105437200-105448600	Weak transcription	Pancreatic Islets	Pancreatic Islet
23	chr12:105439600-105446800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
24	chr12:105439800-105446800	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
25	chr12:105440200-105445800	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
26	chr12:105440200-105449800	Strong transcription	HSMMtube	muscle
27	chr12:105440400-105446000	Strong transcription	Foreskin Melanocyte Primary Cells skin01	Skin
28	chr12:105440400-105446600	Strong transcription	Muscle Satellite Cultured Cells	--
29	chr12:105440400-105446800	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
30	chr12:105440400-105448600	Strong transcription	HSMM	muscle
31	chr12:105441200-105446800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
32	chr12:105441200-105477000	Weak transcription	Gastric	stomach
33	chr12:105441400-105446800	Weak transcription	Placenta	Placenta
34	chr12:105441400-105453400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
35	chr12:105441400-105454800	Weak transcription	Pancreas	Pancrea
36	chr12:105441600-105448800	Weak transcription	A549	lung
37	chr12:105441600-105458200	Weak transcription	Right Ventricle	heart
38	chr12:105441800-105446600	Strong transcription	NHLF	lung
39	chr12:105442400-105448400	Weak transcription	Aorta	Aorta
40	chr12:105442400-105448800	Weak transcription	Fetal Muscle Leg	muscle
41	chr12:105442400-105451000	Weak transcription	Fetal Brain Male	brain
42	chr12:105442400-105469800	Weak transcription	Fetal Lung	lung
43	chr12:105443400-105446800	Weak transcription	Brain Angular Gyrus	brain
44	chr12:105443400-105465000	Weak transcription	H9 Cell Line	embryonic stem cell
45	chr12:105443600-105448800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
46	chr12:105443800-105446400	Weak transcription	Fetal Heart	heart
47	chr12:105443800-105448200	Weak transcription	Brain Germinal Matrix	brain
48	chr12:105443800-105453000	Weak transcription	Rectal Smooth Muscle	rectum
49	chr12:105444000-105453600	Weak transcription	Fetal Muscle Trunk	muscle
50	chr12:105444200-105446600	Weak transcription	Brain Hippocampus Middle	brain

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links