Variant report

Variant	rs61834828
Chromosome Location	chr1:239870769-239870770
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GREM2-6	chr1:239870209-239870822	ENSG00000233355
2	lnc-GREM2-6	chr1:239870424-239871115	ENSG00000233355
3	lnc-GREM2-6	chr1:239870426-239871060	NONHSAT010482
4	lnc-GREM2-6	chr1:239870651-239871060	ENSG00000233355.2

Extended variants
information (count: 60 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:55)

rs_ID	r²[population]
rs1030591	0.92[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10925968	0.88[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10925969	0.88[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1135	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12059584	0.81[AFR][1000 genomes];0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12062155	0.81[AFR][1000 genomes];0.88[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12062192	0.81[AFR][1000 genomes];0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12066872	0.94[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12093210	0.92[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12354162	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13376649	0.85[AFR][1000 genomes];0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16832149	1.00[ASN][1000 genomes]
rs16838584	1.00[ASN][1000 genomes]
rs16838623	1.00[ASN][1000 genomes]
rs16838631	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16838669	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16838681	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16838689	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16838720	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16838848	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16838871	0.88[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16838874	0.88[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16838878	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28448804	0.83[EUR][1000 genomes]
rs4145784	1.00[ASN][1000 genomes]
rs61834772	1.00[ASN][1000 genomes]
rs61834776	1.00[ASN][1000 genomes]
rs61834781	1.00[ASN][1000 genomes]
rs61834783	1.00[ASN][1000 genomes]
rs61834785	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61834786	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61834816	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61834817	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61834821	0.82[AMR][1000 genomes]
rs61834822	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61834823	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61834825	0.98[AFR][1000 genomes];0.92[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61834826	0.92[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61834837	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61834838	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61834839	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61834840	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61834842	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61834844	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61834845	0.88[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61834846	0.88[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61834847	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61836595	1.00[ASN][1000 genomes]
rs61836669	0.94[EUR][1000 genomes]
rs62634805	0.81[AMR][1000 genomes]
rs6661636	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6694025	1.00[ASN][1000 genomes]
rs7516378	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7523711	1.00[ASN][1000 genomes]
rs7527723	0.82[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[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	nsv549435	chr1:239375010-239974006	Active TSS Weak transcription Enhancers Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	esv3377526	chr1:239623743-240111639	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	4 gene(s)	inside rSNPs	diseases
3	nsv873351	chr1:239636613-240324200	Weak transcription Enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
4	esv2757778	chr1:239766094-240389504	Strong transcription Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Active TSS Flanking Active TSS Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases
5	esv2759009	chr1:239766094-240389504	Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription ZNF genes & repeats Strong transcription Active TSS Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:33 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:239845000-239879800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
2	chr1:239861200-239878000	Weak transcription	Fetal Intestine Small	intestine
3	chr1:239861400-239871600	Weak transcription	Primary hematopoietic stem cells	blood
4	chr1:239866800-239875000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
5	chr1:239867400-239879000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
6	chr1:239867600-239875800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
7	chr1:239867800-239879000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
8	chr1:239868000-239871200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
9	chr1:239868000-239871400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chr1:239868000-239871800	Strong transcription	Dnd41	blood
11	chr1:239868400-239870800	Strong transcription	Primary T cells fromperipheralblood	blood
12	chr1:239868400-239871400	Weak transcription	Thymus	Thymus
13	chr1:239868400-239872200	Strong transcription	Primary T helper cells fromperipheralblood	blood
14	chr1:239868600-239878200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
15	chr1:239868800-239880400	Weak transcription	Rectal Mucosa Donor 29	rectum
16	chr1:239869000-239875800	Weak transcription	Colon Smooth Muscle	Colon
17	chr1:239869000-239876000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
18	chr1:239869000-239880800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
19	chr1:239870000-239870800	Weak transcription	Duodenum Smooth Muscle	Duodenum
20	chr1:239870000-239871600	Strong transcription	Primary T cells from cord blood	blood
21	chr1:239870200-239871400	Weak transcription	H9 Cell Line	embryonic stem cell
22	chr1:239870200-239871600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
23	chr1:239870200-239874000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
24	chr1:239870200-239874400	Weak transcription	HUES6 Cell Line	embryonic stem cell
25	chr1:239870200-239874800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
26	chr1:239870200-239875000	Weak transcription	H1 Cell Line	embryonic stem cell
27	chr1:239870200-239875000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
28	chr1:239870200-239875000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
29	chr1:239870200-239875000	Weak transcription	Primary T helper cells PMA-I stimulated	--
30	chr1:239870200-239876200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr1:239870200-239882400	Weak transcription	Pancreas	Pancrea
32	chr1:239870200-239883000	Weak transcription	Fetal Brain Male	brain
33	chr1:239870200-239883000	Weak transcription	Gastric	stomach

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