Variant report

Variant	rs7148326
Chromosome Location	chr14:32969105-32969106
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 10 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:8)

rs_ID	r²[population]
rs17412060	0.86[AMR][1000 genomes];0.96[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs17412116	0.84[AFR][1000 genomes];0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs60217119	0.86[ASN][1000 genomes]
rs61982982	0.86[ASN][1000 genomes]
rs61982983	0.86[ASN][1000 genomes]
rs8014051	0.86[ASN][1000 genomes]
rs8017798	0.86[ASN][1000 genomes]
rs8018953	0.86[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2758352	chr14:32858480-33016442	Enhancers Weak transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	esv2759978	chr14:32858480-33016442	Enhancers Active TSS Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:28 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:32964400-32969200	Weak transcription	Fetal Lung	lung
2	chr14:32964600-32969200	Weak transcription	Hela-S3	cervix
3	chr14:32964800-32969800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
4	chr14:32965000-32970600	Weak transcription	Aorta	Aorta
5	chr14:32965400-32976400	Weak transcription	HSMM	muscle
6	chr14:32966000-32969400	Weak transcription	Rectal Smooth Muscle	rectum
7	chr14:32966400-32969200	Weak transcription	Brain Substantia Nigra	brain
8	chr14:32966400-32969400	Weak transcription	Brain Anterior Caudate	brain
9	chr14:32966400-32969400	Weak transcription	Brain Hippocampus Middle	brain
10	chr14:32966400-32969400	Weak transcription	Brain Inferior Temporal Lobe	brain
11	chr14:32966400-32976800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
12	chr14:32966600-32969200	Weak transcription	Colon Smooth Muscle	Colon
13	chr14:32966600-32969400	Weak transcription	Brain Cingulate Gyrus	brain
14	chr14:32966600-32971200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
15	chr14:32966600-32976400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
16	chr14:32966800-32969200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
17	chr14:32967200-32969600	Enhancers	Fetal Heart	heart
18	chr14:32967200-32969600	Weak transcription	Osteobl	bone
19	chr14:32967200-32978400	Weak transcription	Fetal Muscle Leg	muscle
20	chr14:32967400-32969400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
21	chr14:32968000-32969600	Weak transcription	Skeletal Muscle Female	skeletal muscle
22	chr14:32968000-32975600	Weak transcription	Left Ventricle	heart
23	chr14:32968200-32969400	Weak transcription	HSMMtube	muscle
24	chr14:32968200-32978400	Weak transcription	Psoas Muscle	Psoas
25	chr14:32968400-32969400	Weak transcription	Brain Angular Gyrus	brain
26	chr14:32968400-32969600	Weak transcription	Right Atrium	heart
27	chr14:32968800-32969600	Weak transcription	Right Ventricle	heart
28	chr14:32969000-32971200	Enhancers	Skeletal Muscle Male	skeletal muscle

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