Variant report

Variant	rs756032
Chromosome Location	chr18:44292667-44292668
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	chr18:44290160..44292978-chr18:44295020..44296704,2	K562	blood:

Extended variants
information (count: 19 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:7)

rs_ID	r²[population]
rs12957855	0.97[AMR][1000 genomes];0.91[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12960641	0.92[AMR][1000 genomes];0.90[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs481297	0.87[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs4890684	0.90[AFR][1000 genomes];0.91[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs57464683	0.97[AMR][1000 genomes];0.89[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9950834	0.87[EUR][1000 genomes]
rs9961033	0.91[AFR][1000 genomes];0.93[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:12 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv428355	chr18:44160181-44406285	Weak transcription Bivalent Enhancer Flanking Active TSS Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	5 gene(s)	inside rSNPs	diseases
2	nsv9629	chr18:44264693-44757511	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
3	nsv909589	chr18:44279892-44330604	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Active TSS	TF binding region Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	nsv909590	chr18:44279892-44332911	Weak transcription Flanking Active TSS Enhancers Active TSS Bivalent Enhancer ZNF genes & repeats Strong transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
5	nsv909591	chr18:44279892-44370518	Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
6	nsv909592	chr18:44279892-44385150	Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
7	nsv909593	chr18:44279892-44396246	Weak transcription Enhancers Bivalent Enhancer Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	4 gene(s)	inside rSNPs	diseases
8	nsv909594	chr18:44279892-44400621	Weak transcription Enhancers Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	4 gene(s)	inside rSNPs	diseases
9	nsv909595	chr18:44279892-44422661	Enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	4 gene(s)	inside rSNPs	diseases
10	nsv909596	chr18:44291419-44330604	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
11	nsv909597	chr18:44291419-44385150	Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
12	nsv909598	chr18:44291419-44422661	Strong transcription Weak transcription Enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:39 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:44286800-44298800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr18:44287800-44298800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr18:44290000-44293600	Enhancers	Psoas Muscle	Psoas
4	chr18:44290000-44295400	Enhancers	Fetal Muscle Leg	muscle
5	chr18:44290600-44293200	Enhancers	Right Atrium	heart
6	chr18:44290600-44293600	Enhancers	Fetal Muscle Trunk	muscle
7	chr18:44290600-44293600	Enhancers	Left Ventricle	heart
8	chr18:44290600-44294600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
9	chr18:44290800-44292800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
10	chr18:44290800-44293800	Enhancers	HSMMtube	muscle
11	chr18:44291000-44293000	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
12	chr18:44291000-44293400	Enhancers	NHDF-Ad	bronchial
13	chr18:44291000-44293600	Enhancers	Brain Angular Gyrus	brain
14	chr18:44291200-44293000	Enhancers	Muscle Satellite Cultured Cells	--
15	chr18:44291200-44293000	Enhancers	Brain Inferior Temporal Lobe	brain
16	chr18:44291200-44293400	Enhancers	HSMM	muscle
17	chr18:44291400-44292800	Bivalent Enhancer	Fetal Stomach	stomach
18	chr18:44291400-44293000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr18:44291400-44293000	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
20	chr18:44291400-44293200	Enhancers	Brain Cingulate Gyrus	brain
21	chr18:44291600-44293000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
22	chr18:44291600-44293000	Enhancers	Brain Hippocampus Middle	brain
23	chr18:44291600-44293000	Enhancers	Ovary	ovary
24	chr18:44291600-44293200	Enhancers	Brain Substantia Nigra	brain
25	chr18:44291600-44293400	Enhancers	NH-A	brain
26	chr18:44291600-44293600	Enhancers	Cortex derived primary cultured neurospheres	brain
27	chr18:44291800-44293000	Enhancers	Right Ventricle	heart
28	chr18:44291800-44293200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
29	chr18:44291800-44293200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
30	chr18:44291800-44293200	Enhancers	NHLF	lung
31	chr18:44291800-44293200	Enhancers	Osteobl	bone
32	chr18:44291800-44295200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
33	chr18:44292000-44292800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
34	chr18:44292000-44293800	Enhancers	Fetal Heart	heart
35	chr18:44292000-44294400	Enhancers	Brain Germinal Matrix	brain
36	chr18:44292000-44295000	Weak transcription	H1 Cell Line	embryonic stem cell
37	chr18:44292200-44294400	Enhancers	Skeletal Muscle Female	skeletal muscle
38	chr18:44292400-44293000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
39	chr18:44292600-44293000	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links