Variant report

Variant	rs941746
Chromosome Location	chr14:32904928-32904929
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr14:32904805..32907044-chr14:32912788..32914378,2	K562	blood:

Extended variants
information (count: 33 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:31)

rs_ID	r²[population]
rs10130628	0.86[JPT][hapmap]
rs10136333	0.85[CEU][hapmap]
rs11156745	0.91[ASN][1000 genomes]
rs11156746	0.89[ASN][1000 genomes]
rs11628453	0.92[ASN][1000 genomes]
rs17409829	0.88[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs1815234	0.82[EUR][1000 genomes]
rs1951189	0.82[CEU][hapmap];0.95[CHB][hapmap];0.86[JPT][hapmap];0.85[AMR][1000 genomes];0.88[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1951191	0.82[AFR][1000 genomes];0.98[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1957013	0.97[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1957015	0.96[CEU][hapmap];1.00[CHB][hapmap];0.93[CHD][hapmap];0.90[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.98[TSI][hapmap];0.99[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1957016	0.97[ASN][1000 genomes]
rs1957018	1.00[CHB][hapmap];0.95[CHD][hapmap];0.91[JPT][hapmap];0.84[MEX][hapmap];0.97[ASN][1000 genomes]
rs1957019	0.91[AMR][1000 genomes];0.90[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1957020	0.83[CHB][hapmap]
rs2224430	1.00[CHB][hapmap];0.95[JPT][hapmap];0.97[ASN][1000 genomes]
rs2383302	0.86[ASW][hapmap];1.00[CEU][hapmap];0.97[GIH][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];0.85[MKK][hapmap];0.98[TSI][hapmap];0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs3784191	0.81[CHD][hapmap];0.82[JPT][hapmap]
rs4329831	0.80[AMR][1000 genomes];0.84[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs56837786	0.82[ASN][1000 genomes]
rs6571518	0.95[CHB][hapmap];0.95[CHD][hapmap];0.90[JPT][hapmap];0.84[MEX][hapmap];0.97[ASN][1000 genomes]
rs71419908	1.00[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs7146377	0.95[CHB][hapmap];0.95[CHD][hapmap];1.00[YRI][hapmap];0.80[ASN][1000 genomes]
rs7147629	1.00[YRI][hapmap];0.97[ASN][1000 genomes]
rs7157869	0.91[JPT][hapmap]
rs8013463	0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9285570	0.95[CHB][hapmap];0.95[CHD][hapmap]
rs941747	0.83[EUR][1000 genomes]
rs941748	0.83[EUR][1000 genomes]
rs9972146	0.82[ASN][1000 genomes]
rs9972147	0.80[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:33 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:32897600-32908400	Weak transcription	Fetal Brain Female	brain
2	chr14:32898000-32906200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
3	chr14:32898200-32908200	Weak transcription	Right Atrium	heart
4	chr14:32898400-32908400	Weak transcription	Psoas Muscle	Psoas
5	chr14:32899000-32913400	Weak transcription	Fetal Lung	lung
6	chr14:32899600-32906200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
7	chr14:32899800-32907400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr14:32900000-32905800	Weak transcription	Cortex derived primary cultured neurospheres	brain
9	chr14:32901800-32907800	Active TSS	Aorta	Aorta
10	chr14:32902800-32905800	Active TSS	Duodenum Smooth Muscle	Duodenum
11	chr14:32902800-32907200	Weak transcription	Skeletal Muscle Male	skeletal muscle
12	chr14:32902800-32907400	Weak transcription	Fetal Heart	heart
13	chr14:32903000-32906200	Weak transcription	Right Ventricle	heart
14	chr14:32903000-32907000	Weak transcription	Small Intestine	intestine
15	chr14:32903000-32910200	Weak transcription	Esophagus	oesophagus
16	chr14:32903400-32906400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
17	chr14:32903400-32908200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
18	chr14:32903600-32908600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
19	chr14:32903800-32906400	Weak transcription	Left Ventricle	heart
20	chr14:32903800-32907200	Weak transcription	Rectal Smooth Muscle	rectum
21	chr14:32904200-32905600	Weak transcription	Brain Angular Gyrus	brain
22	chr14:32904200-32905800	Weak transcription	Brain Cingulate Gyrus	brain
23	chr14:32904400-32905200	Weak transcription	Colon Smooth Muscle	Colon
24	chr14:32904400-32905400	Weak transcription	Brain Hippocampus Middle	brain
25	chr14:32904400-32905400	Weak transcription	Brain Substantia Nigra	brain
26	chr14:32904400-32907200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
27	chr14:32904400-32908000	Weak transcription	Ovary	ovary
28	chr14:32904400-32908600	Weak transcription	Rectal Mucosa Donor 31	rectum
29	chr14:32904600-32905600	Weak transcription	Brain Anterior Caudate	brain
30	chr14:32904600-32905600	Weak transcription	Stomach Smooth Muscle	stomach
31	chr14:32904600-32906800	Weak transcription	GM12878-XiMat	blood
32	chr14:32904600-32913400	Weak transcription	Brain Germinal Matrix	brain
33	chr14:32904800-32905600	Weak transcription	Brain Inferior Temporal Lobe	brain

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