Variant report

Variant	rs4331115
Chromosome Location	chr11:119650848-119650849
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	chr11:119645625..119647628-chr11:119648979..119651393,2	K562	blood:

Extended variants
information (count: 49 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:47)

rs_ID	r²[population]
rs10790344	0.81[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs10790345	0.83[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs10892453	0.83[ASN][1000 genomes]
rs10892454	0.90[EUR][1000 genomes]
rs10892456	0.82[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs10892457	0.81[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs10892458	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs10892459	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10892460	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10892461	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11217495	0.94[EUR][1000 genomes]
rs11217501	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11217502	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11217503	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11606569	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12222723	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs12803325	0.96[ASN][1000 genomes]
rs1466051	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1466052	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs34033074	0.95[ASN][1000 genomes]
rs34228131	0.97[ASN][1000 genomes]
rs35121417	0.83[EUR][1000 genomes]
rs35662046	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4258392	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs4269933	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs4301801	0.82[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs4341549	0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4388901	0.97[ASN][1000 genomes]
rs4408323	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs4418818	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs4420283	0.96[ASN][1000 genomes]
rs4608095	0.82[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs5020632	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs5020633	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs5026369	0.81[AFR][1000 genomes];0.99[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs59814528	0.81[ASN][1000 genomes]
rs6589772	0.86[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6589774	0.96[ASN][1000 genomes]
rs6589776	0.90[EUR][1000 genomes]
rs67007544	0.92[AFR][1000 genomes];0.96[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7103360	0.96[AFR][1000 genomes];0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7110679	0.80[EUR][1000 genomes]
rs7926574	0.95[EUR][1000 genomes]
rs7929505	0.96[ASN][1000 genomes]
rs7936400	0.98[EUR][1000 genomes]
rs7942259	0.83[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs9326253	0.93[EUR][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	nsv898423	chr11:119541332-119659753	Flanking Active TSS ZNF genes & repeats Enhancers Weak transcription Bivalent Enhancer Bivalent/Poised TSS Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
2	nsv528824	chr11:119650105-119661809	Enhancers Bivalent Enhancer Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:17 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:119641400-119652600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr11:119645200-119652800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chr11:119647000-119654400	Enhancers	Fetal Heart	heart
4	chr11:119648600-119653200	Enhancers	Right Ventricle	heart
5	chr11:119649600-119652600	Weak transcription	GM12878-XiMat	blood
6	chr11:119649600-119653000	Weak transcription	Brain Inferior Temporal Lobe	brain
7	chr11:119649600-119653400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
8	chr11:119650000-119651000	Weak transcription	Left Ventricle	heart
9	chr11:119650000-119651400	Enhancers	Breast Myoepithelial Primary Cells	Breast
10	chr11:119650000-119651400	Bivalent Enhancer	Fetal Stomach	stomach
11	chr11:119650000-119652600	Enhancers	Right Atrium	heart
12	chr11:119650200-119651400	Enhancers	Ovary	ovary
13	chr11:119650400-119651000	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
14	chr11:119650400-119651400	Bivalent Enhancer	HSMMtube	muscle
15	chr11:119650400-119653200	Enhancers	Fetal Muscle Leg	muscle
16	chr11:119650800-119651200	Enhancers	Fetal Lung	lung
17	chr11:119650800-119652200	Enhancers	Fetal Muscle Trunk	muscle

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