Variant report

Variant	rs233061
Chromosome Location	chr1:85799282-85799283
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 84 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:82)

rs_ID	r²[population]
rs1001604	0.87[EUR][1000 genomes]
rs10489513	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11161607	0.83[EUR][1000 genomes]
rs11161611	0.84[EUR][1000 genomes]
rs1146379	0.92[ASN][1000 genomes]
rs12044537	0.84[AMR][1000 genomes];0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12047422	0.85[EUR][1000 genomes]
rs12124170	0.91[EUR][1000 genomes]
rs12140103	0.84[EUR][1000 genomes]
rs1498373	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs1498375	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs1554597	0.84[EUR][1000 genomes]
rs173026	0.84[AFR][1000 genomes];0.87[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs18582	0.83[AFR][1000 genomes];0.93[EUR][1000 genomes]
rs1884139	0.85[EUR][1000 genomes]
rs2011825	0.85[EUR][1000 genomes]
rs2012683	0.86[EUR][1000 genomes]
rs2177461	0.84[EUR][1000 genomes]
rs2207368	0.86[EUR][1000 genomes]
rs2268667	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs2300634	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs2300637	0.91[EUR][1000 genomes]
rs233047	0.91[EUR][1000 genomes]
rs233050	0.86[EUR][1000 genomes]
rs233053	0.85[AMR][1000 genomes];0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs233054	0.86[EUR][1000 genomes]
rs233055	0.90[AFR][1000 genomes];0.99[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs233057	0.90[AFR][1000 genomes];0.89[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs233058	0.90[AFR][1000 genomes];0.89[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs233059	0.90[AFR][1000 genomes];0.89[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs233060	0.90[AFR][1000 genomes];0.89[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs233062	0.90[AFR][1000 genomes];0.89[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs233066	0.80[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs233067	0.82[AFR][1000 genomes];0.84[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs233068	0.95[AFR][1000 genomes];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs233069	0.83[AFR][1000 genomes];0.82[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs233071	0.95[AFR][1000 genomes];0.82[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs233072	0.97[AFR][1000 genomes];0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs233074	0.85[EUR][1000 genomes]
rs233091	0.92[AFR][1000 genomes];0.91[EUR][1000 genomes]
rs233093	0.91[EUR][1000 genomes]
rs233095	0.91[EUR][1000 genomes]
rs233097	0.91[AFR][1000 genomes];0.87[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs233099	0.83[AFR][1000 genomes];0.91[EUR][1000 genomes]
rs233108	0.84[AFR][1000 genomes];0.86[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs233109	0.87[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs233112	0.93[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs233113	0.91[AFR][1000 genomes];0.87[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs233114	0.91[AFR][1000 genomes];0.87[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs233115	0.86[AFR][1000 genomes];0.86[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs233118	0.93[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs233119	0.89[AFR][1000 genomes];0.87[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs233120	0.86[AFR][1000 genomes];0.87[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs233121	0.87[AFR][1000 genomes];0.87[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs233124	0.93[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs233127	0.85[AFR][1000 genomes];0.86[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs233130	0.90[AFR][1000 genomes];0.89[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs233131	0.90[AFR][1000 genomes];0.89[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs233132	0.90[AFR][1000 genomes];0.89[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs233133	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2474123	0.81[EUR][1000 genomes]
rs2892888	0.83[EUR][1000 genomes]
rs3087894	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs3768227	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs3949301	0.84[EUR][1000 genomes]
rs423105	0.90[AFR][1000 genomes];0.89[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs4949890	0.91[EUR][1000 genomes]
rs4949900	0.84[EUR][1000 genomes]
rs506082	0.84[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6576763	0.88[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6576764	0.84[EUR][1000 genomes]
rs6576765	0.80[AMR][1000 genomes];0.87[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6576766	0.83[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6576767	0.82[EUR][1000 genomes]
rs6657817	0.84[EUR][1000 genomes]
rs6671599	0.84[EUR][1000 genomes]
rs66811655	0.90[EUR][1000 genomes]
rs6704103	0.83[EUR][1000 genomes]
rs67611930	0.86[EUR][1000 genomes]
rs72724606	0.85[EUR][1000 genomes]
rs761601	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs997251	0.86[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	nsv1006994	chr1:85454304-86327679	Active TSS Enhancers Weak transcription Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	72 gene(s)	inside rSNPs	diseases
2	esv34165	chr1:85542040-85846249	Flanking Active TSS Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Strong transcription Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	30 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:40 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:85790600-85800000	Enhancers	HUVEC	blood vessel
2	chr1:85792200-85806000	Weak transcription	Fetal Kidney	kidney
3	chr1:85796200-85799800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr1:85796600-85799600	Enhancers	Osteobl	bone
5	chr1:85796600-85801800	Weak transcription	Gastric	stomach
6	chr1:85796600-85804000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
7	chr1:85796600-85809400	Weak transcription	Stomach Mucosa	stomach
8	chr1:85796800-85799600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
9	chr1:85796800-85804200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
10	chr1:85796800-85805400	Weak transcription	Aorta	Aorta
11	chr1:85796800-85805400	Weak transcription	HepG2	liver
12	chr1:85796800-85806400	Weak transcription	Small Intestine	intestine
13	chr1:85796800-85809600	Weak transcription	Rectal Mucosa Donor 31	rectum
14	chr1:85797000-85800600	Weak transcription	HMEC	breast
15	chr1:85797000-85805000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr1:85797400-85800200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
17	chr1:85797600-85800400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
18	chr1:85797600-85803600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr1:85798200-85799600	Weak transcription	Cortex derived primary cultured neurospheres	brain
20	chr1:85798200-85800400	Weak transcription	NH-A	brain
21	chr1:85798400-85803400	Weak transcription	Hela-S3	cervix
22	chr1:85798400-85804200	Weak transcription	Right Ventricle	heart
23	chr1:85798400-85806200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
24	chr1:85798600-85800200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
25	chr1:85798600-85800200	Weak transcription	HSMMtube	muscle
26	chr1:85798800-85799600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
27	chr1:85798800-85800200	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
28	chr1:85798800-85800600	ZNF genes & repeats	Primary B cells from peripheral blood	blood
29	chr1:85798800-85808400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
30	chr1:85798800-85808400	Weak transcription	Ovary	ovary
31	chr1:85798800-85824800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
32	chr1:85798800-85824800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
33	chr1:85799000-85799400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
34	chr1:85799000-85800200	ZNF genes & repeats	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
35	chr1:85799000-85800200	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
36	chr1:85799000-85800400	Weak transcription	Fetal Stomach	stomach
37	chr1:85799000-85813600	Weak transcription	Fetal Intestine Large	intestine
38	chr1:85799200-85799600	Weak transcription	Fetal Intestine Small	intestine
39	chr1:85799200-85799600	Weak transcription	HSMM	muscle
40	chr1:85799200-85800200	Strong transcription	Muscle Satellite Cultured Cells	--

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