Variant report

Variant	rs41300027
Chromosome Location	chr1:213057516-213057517
allele	C/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:21)

rs_ID	r²[population]
rs2047288	1.00[AFR][1000 genomes];0.85[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2047291	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2088256	1.00[AFR][1000 genomes]
rs3768549	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs41258005	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs41296666	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs41296668	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs41296674	1.00[AFR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs41296676	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs41296678	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs41296680	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs41297452	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs41300033	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs41300035	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs41300043	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs41300979	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs41301029	1.00[AFR][1000 genomes];0.85[AMR][1000 genomes];0.96[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs41307644	0.92[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs41307646	1.00[AFR][1000 genomes];0.92[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs41314542	1.00[AFR][1000 genomes];0.92[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs58746017	1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1011186	chr1:213005165-213069563	Flanking Active TSS Weak transcription Active TSS Strong transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
2	nsv1013705	chr1:213005344-213064209	Flanking Active TSS Weak transcription Genic enhancers Active TSS Strong transcription Enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
3	nsv1008383	chr1:213025546-213114894	Strong transcription Active TSS Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
4	nsv998261	chr1:213029814-213064209	Strong transcription Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Active TSS Enhancers Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
5	nsv998979	chr1:213029814-213073013	Enhancers Genic enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
6	nsv1007129	chr1:213037244-213083261	Weak transcription Enhancers Strong transcription Genic enhancers Active TSS ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:125 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:213032600-213073000	Weak transcription	Colonic Mucosa	Colon
2	chr1:213032600-213073000	Weak transcription	Esophagus	oesophagus
3	chr1:213032800-213057800	Weak transcription	Placenta	Placenta
4	chr1:213032800-213061800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr1:213032800-213062000	Weak transcription	Psoas Muscle	Psoas
6	chr1:213033600-213062000	Weak transcription	Thymus	Thymus
7	chr1:213034400-213058000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
8	chr1:213034400-213068000	Weak transcription	Colon Smooth Muscle	Colon
9	chr1:213034600-213061800	Weak transcription	Fetal Heart	heart
10	chr1:213034600-213067800	Weak transcription	NHLF	lung
11	chr1:213034600-213070600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
12	chr1:213035800-213073000	Weak transcription	Small Intestine	intestine
13	chr1:213036000-213070800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr1:213036200-213062000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
15	chr1:213036400-213062000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
16	chr1:213037600-213073200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
17	chr1:213038400-213072000	Weak transcription	Pancreatic Islets	Pancreatic Islet
18	chr1:213039600-213073000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
19	chr1:213040400-213073000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
20	chr1:213043200-213062000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
21	chr1:213043200-213073400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr1:213044400-213063200	Weak transcription	Placenta Amnion	Placenta Amnion
23	chr1:213045000-213070800	Weak transcription	Pancreas	Pancrea
24	chr1:213046600-213066400	Strong transcription	Primary monocytes fromperipheralblood	blood
25	chr1:213047000-213073600	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
26	chr1:213047200-213059600	Weak transcription	Brain Angular Gyrus	brain
27	chr1:213047200-213061800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
28	chr1:213047200-213062000	Weak transcription	Brain Cingulate Gyrus	brain
29	chr1:213047400-213059200	Weak transcription	HUVEC	blood vessel
30	chr1:213048800-213062600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
31	chr1:213049000-213058000	Weak transcription	Osteobl	bone
32	chr1:213049000-213059200	Weak transcription	Stomach Smooth Muscle	stomach
33	chr1:213049000-213061800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
34	chr1:213049000-213073000	Weak transcription	HSMMtube	muscle
35	chr1:213049400-213063200	Weak transcription	Skeletal Muscle Male	skeletal muscle
36	chr1:213049600-213058000	Weak transcription	A549	lung
37	chr1:213049600-213059600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
38	chr1:213049600-213062000	Weak transcription	Rectal Smooth Muscle	rectum
39	chr1:213049800-213059400	Weak transcription	Primary T cells from cord blood	blood
40	chr1:213049800-213059600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
41	chr1:213049800-213061800	Weak transcription	Ovary	ovary
42	chr1:213049800-213062000	Weak transcription	Gastric	stomach
43	chr1:213049800-213062600	Weak transcription	NHEK	skin
44	chr1:213049800-213072400	Weak transcription	Fetal Brain Male	brain
45	chr1:213049800-213073200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
46	chr1:213049800-213073200	Weak transcription	Spleen	Spleen
47	chr1:213050000-213065000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
48	chr1:213050800-213065800	Strong transcription	Monocytes-CD14+_RO01746	blood
49	chr1:213051200-213064400	Strong transcription	Hela-S3	cervix
50	chr1:213051600-213060600	Weak transcription	NH-A	brain

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