Variant report

Variant	rs10735738
Chromosome Location	chr14:33080251-33080252
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 29 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:26)

rs_ID	r²[population]
rs10138218	0.82[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11156754	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11626762	0.82[ASN][1000 genomes]
rs12717222	0.96[ASN][1000 genomes]
rs17099309	0.86[ASN][1000 genomes]
rs17099320	0.86[ASN][1000 genomes]
rs17099324	0.86[ASN][1000 genomes]
rs17099326	0.89[ASN][1000 genomes]
rs1956212	0.86[ASN][1000 genomes]
rs1956219	0.81[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs3784203	1.00[ASN][1000 genomes]
rs4981992	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4981993	0.80[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61981363	0.89[ASN][1000 genomes]
rs61983021	0.86[ASN][1000 genomes]
rs6571540	0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6571541	0.81[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7146517	0.96[ASN][1000 genomes]
rs7154753	0.80[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7157328	0.80[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7157533	0.82[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7157744	0.82[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7160156	0.96[ASN][1000 genomes]
rs73255099	0.89[ASN][1000 genomes]
rs8017249	0.82[ASN][1000 genomes]
rs979494	0.82[ASN][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	nsv1045035	chr14:32986003-33543227	Weak transcription Enhancers Flanking Bivalent TSS/Enh Genic enhancers Flanking Active TSS Bivalent/Poised TSS Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
2	nsv542021	chr14:32986003-33543227	Active TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
3	nsv428624	chr14:33065571-33214223	Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 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	chr14:33072200-33103600	Weak transcription	Fetal Muscle Trunk	muscle
2	chr14:33072400-33091800	Weak transcription	Left Ventricle	heart
3	chr14:33075600-33081600	Enhancers	Skeletal Muscle Female	skeletal muscle
4	chr14:33076000-33083200	Enhancers	NHDF-Ad	bronchial
5	chr14:33076600-33081200	Enhancers	Fetal Heart	heart
6	chr14:33076800-33080800	Weak transcription	Duodenum Smooth Muscle	Duodenum
7	chr14:33077600-33082400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr14:33077800-33081600	Enhancers	Osteobl	bone
9	chr14:33078000-33080400	Weak transcription	HSMM	muscle
10	chr14:33078000-33080800	Weak transcription	Rectal Smooth Muscle	rectum
11	chr14:33078000-33081000	Enhancers	Brain Anterior Caudate	brain
12	chr14:33078200-33081600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
13	chr14:33078600-33080400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
14	chr14:33078600-33080600	Weak transcription	NHEK	skin
15	chr14:33078800-33080400	Weak transcription	Cortex derived primary cultured neurospheres	brain
16	chr14:33078800-33080400	Weak transcription	Brain Angular Gyrus	brain
17	chr14:33078800-33080600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
18	chr14:33078800-33080600	Weak transcription	Skeletal Muscle Male	skeletal muscle
19	chr14:33078800-33080600	Weak transcription	NH-A	brain
20	chr14:33078800-33080800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
21	chr14:33078800-33097000	Weak transcription	Brain Inferior Temporal Lobe	brain
22	chr14:33078800-33098200	Weak transcription	Fetal Muscle Leg	muscle
23	chr14:33078800-33102600	Weak transcription	Aorta	Aorta
24	chr14:33079000-33080400	Weak transcription	NHLF	lung
25	chr14:33079000-33080800	Weak transcription	Fetal Stomach	stomach
26	chr14:33079200-33080400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
27	chr14:33079400-33080400	Weak transcription	Muscle Satellite Cultured Cells	--
28	chr14:33079800-33080800	Weak transcription	Brain Hippocampus Middle	brain
29	chr14:33079800-33080800	Weak transcription	Psoas Muscle	Psoas
30	chr14:33079800-33081000	Enhancers	Brain Cingulate Gyrus	brain
31	chr14:33080000-33081400	Enhancers	Colon Smooth Muscle	Colon
32	chr14:33080000-33081600	Enhancers	HSMMtube	muscle
33	chr14:33080000-33104200	Weak transcription	Stomach Smooth Muscle	stomach
34	chr14:33080200-33081400	Enhancers	Brain Substantia Nigra	brain
35	chr14:33080200-33081600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
36	chr14:33080200-33081600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
37	chr14:33080200-33081800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chr14:33080200-33081800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
39	chr14:33080200-33081800	Enhancers	HMEC	breast

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