Variant report

Variant	rs1881411
Chromosome Location	chr2:145771247-145771248
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 27 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:22)

rs_ID	r²[population]
rs10204459	0.83[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs12993495	0.94[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12996204	0.88[AFR][1000 genomes];0.92[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs1347828	0.90[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs1528412	0.87[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs1528413	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs16855349	0.88[AFR][1000 genomes];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs1898731	0.81[AFR][1000 genomes];0.94[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs2243647	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs2243648	0.87[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs2246114	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs2246142	0.87[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs2246245	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs2249681	0.81[AFR][1000 genomes];0.94[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs2249798	0.82[AFR][1000 genomes];0.94[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs2249819	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs2250164	0.81[AFR][1000 genomes];0.93[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs2250518	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2250546	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2579024	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs718229	0.89[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs7589308	0.81[AMR][1000 genomes];0.91[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1002563	chr2:145182201-145863253	Enhancers Weak transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Active TSS Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
2	nsv535957	chr2:145182201-145863253	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
3	nsv932113	chr2:145515124-145844491	Flanking Active TSS Enhancers Weak transcription Active TSS Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	nsv834398	chr2:145659419-145830156	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
5	nsv431768	chr2:145741527-145981491	Flanking Active TSS Weak transcription Enhancers Active TSS Strong transcription 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:28 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:145768000-145772000	Enhancers	Fetal Heart	heart
2	chr2:145768400-145771600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr2:145769400-145772000	Weak transcription	Right Atrium	heart
4	chr2:145770000-145780400	Weak transcription	Ovary	ovary
5	chr2:145770200-145771400	Weak transcription	Psoas Muscle	Psoas
6	chr2:145770200-145771800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
7	chr2:145770400-145773200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
8	chr2:145770400-145774400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr2:145770400-145778200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
10	chr2:145770600-145771600	Enhancers	A549	lung
11	chr2:145770600-145771800	Enhancers	HUVEC	blood vessel
12	chr2:145770600-145772800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
13	chr2:145770600-145779200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
14	chr2:145770600-145779400	Weak transcription	Fetal Lung	lung
15	chr2:145770600-145779600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
16	chr2:145770800-145771400	Enhancers	iPS-18 Cell Line	embryonic stem cell
17	chr2:145770800-145771800	Weak transcription	H9 Cell Line	embryonic stem cell
18	chr2:145770800-145772800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr2:145770800-145772800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
20	chr2:145770800-145772800	Weak transcription	NH-A	brain
21	chr2:145770800-145773000	Weak transcription	Osteobl	bone
22	chr2:145770800-145774200	Weak transcription	Hela-S3	cervix
23	chr2:145770800-145774200	Weak transcription	NHDF-Ad	bronchial
24	chr2:145770800-145774800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
25	chr2:145770800-145776200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
26	chr2:145771000-145772800	Weak transcription	Muscle Satellite Cultured Cells	--
27	chr2:145771200-145774400	Weak transcription	Aorta	Aorta
28	chr2:145771200-145782600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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