Variant report

Variant	rs794263
Chromosome Location	chr6:119322468-119322469
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:119319940..119322469-chr6:119324553..119327875,4	K562	blood:

Extended variants
information (count: 41 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:40)

rs_ID	r²[population]
rs11967399	0.84[AFR][1000 genomes];0.98[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11967889	0.90[AFR][1000 genomes];0.98[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12526935	0.86[ASN][1000 genomes]
rs1413906	0.85[ASN][1000 genomes]
rs1570493	0.86[ASN][1000 genomes]
rs17513308	0.87[ASN][1000 genomes]
rs1762200	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2051056	0.87[AFR][1000 genomes];0.93[AMR][1000 genomes];0.92[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2051057	0.87[AFR][1000 genomes];0.93[AMR][1000 genomes];0.92[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2295709	0.80[ASN][1000 genomes]
rs2357020	0.92[AFR][1000 genomes];0.98[AMR][1000 genomes];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2357030	0.89[ASN][1000 genomes]
rs2782575	0.99[ASN][1000 genomes]
rs2797352	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2884078	0.87[ASN][1000 genomes]
rs4946383	0.89[AFR][1000 genomes];0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4946388	0.85[ASN][1000 genomes]
rs4946389	0.85[ASN][1000 genomes]
rs4946390	0.85[ASN][1000 genomes]
rs57100274	0.93[AFR][1000 genomes];0.98[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs57285368	0.90[AFR][1000 genomes];0.98[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6931558	0.84[ASN][1000 genomes]
rs7756475	0.85[ASN][1000 genomes]
rs7764418	0.87[ASN][1000 genomes]
rs794260	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs794261	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs794262	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs794264	0.98[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs794266	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs794614	0.83[ASN][1000 genomes]
rs808028	0.85[ASN][1000 genomes]
rs813812	0.97[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9374777	0.83[ASN][1000 genomes]
rs9387629	0.86[ASN][1000 genomes]
rs9387630	0.84[ASN][1000 genomes]
rs9398499	0.86[ASN][1000 genomes]
rs9401113	0.93[AFR][1000 genomes];0.98[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9401118	0.86[ASN][1000 genomes]
rs9481881	0.85[ASN][1000 genomes]
rs954753	0.85[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1030400	chr6:119320153-119433830	Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region miRNA	30 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:26 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:119285800-119340000	Weak transcription	Fetal Brain Male	brain
2	chr6:119287200-119326600	Weak transcription	Fetal Brain Female	brain
3	chr6:119287400-119330000	Weak transcription	Fetal Muscle Leg	muscle
4	chr6:119292400-119344000	Weak transcription	Brain Germinal Matrix	brain
5	chr6:119293200-119345400	Weak transcription	Lung	lung
6	chr6:119294200-119330800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
7	chr6:119300600-119344000	Weak transcription	HUES48 Cell Line	embryonic stem cell
8	chr6:119300800-119342600	Weak transcription	Brain Anterior Caudate	brain
9	chr6:119313000-119329800	Weak transcription	HUES6 Cell Line	embryonic stem cell
10	chr6:119314400-119364400	Weak transcription	Fetal Muscle Trunk	muscle
11	chr6:119315200-119325200	Weak transcription	Pancreas	Pancrea
12	chr6:119315400-119329800	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr6:119315400-119330800	Weak transcription	Brain Inferior Temporal Lobe	brain
14	chr6:119316600-119328800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr6:119318600-119344200	Weak transcription	Fetal Lung	lung
16	chr6:119319400-119330200	Weak transcription	Ovary	ovary
17	chr6:119319600-119333600	Weak transcription	Primary T helper cells PMA-I stimulated	--
18	chr6:119319800-119342600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
19	chr6:119320000-119327000	Weak transcription	Cortex derived primary cultured neurospheres	brain
20	chr6:119320400-119329200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
21	chr6:119321000-119323000	Weak transcription	Fetal Intestine Small	intestine
22	chr6:119321400-119323000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
23	chr6:119321400-119325600	Weak transcription	Pancreatic Islets	Pancreatic Islet
24	chr6:119321800-119322600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
25	chr6:119321800-119322600	Strong transcription	Placenta	Placenta
26	chr6:119321800-119329800	Weak transcription	Fetal Intestine Large	intestine

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