Variant report

Variant	rs2890923
Chromosome Location	chr2:149297930-149297931
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr2:149291312..149293367-chr2:149296532..149298461,2	K562	blood:
2	chr2:149294626..149297219-chr2:149297327..149299085,2	K562	blood:

Extended variants
information (count: 35 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs10164839	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10210601	1.00[CHB][hapmap];0.85[GIH][hapmap]
rs10497036	0.90[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11901990	0.87[AMR][1000 genomes];0.88[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12691798	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1448894	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs16828945	0.87[AMR][1000 genomes];0.90[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs16829008	0.87[AMR][1000 genomes];0.90[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs16829022	0.80[CEU][hapmap];1.00[CHB][hapmap];0.90[CHD][hapmap];1.00[GIH][hapmap];0.86[MEX][hapmap];0.88[TSI][hapmap];0.87[AMR][1000 genomes];0.90[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs16829052	1.00[CHB][hapmap]
rs2382229	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4972370	0.86[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs4972371	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap];0.86[AFR][1000 genomes];0.87[AMR][1000 genomes];0.93[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs6430319	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6430320	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6430321	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6430331	0.80[CEU][hapmap];1.00[CHB][hapmap];1.00[GIH][hapmap];0.86[MEX][hapmap];0.83[EUR][1000 genomes]
rs6712173	0.95[AFR][1000 genomes];0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6715405	0.82[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs6721673	0.84[AFR][1000 genomes];0.87[AMR][1000 genomes];0.93[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs6725114	1.00[CHB][hapmap];1.00[GIH][hapmap]
rs6740827	0.82[CHB][hapmap];0.85[GIH][hapmap]
rs6760718	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7583200	0.80[CEU][hapmap];1.00[CHB][hapmap];0.87[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs7592501	0.87[AMR][1000 genomes];0.90[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7595798	0.86[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs881184	0.80[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1012275	chr2:149031668-149316793	Enhancers Strong transcription Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	esv2751831	chr2:149151358-150105603	Weak transcription Flanking Bivalent TSS/Enh Strong transcription Enhancers Active TSS Bivalent/Poised TSS Flanking Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
3	nsv1000101	chr2:149165813-149361220	Enhancers Strong transcription Genic enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv868861	chr2:149198443-149434604	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
5	nsv917109	chr2:149198443-149948302	ZNF genes & repeats Weak transcription Flanking Active TSS Enhancers Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Bivalent Enhancer Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
6	nsv1004663	chr2:149214090-149373061	Enhancers Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Weak transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
7	esv2762913	chr2:149249683-149345487	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
8	nsv527539	chr2:149283070-149330251	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:35 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:149292800-149310400	Weak transcription	Right Atrium	heart
2	chr2:149295600-149298000	Enhancers	Primary T helper naive cells from peripheral blood	blood
3	chr2:149295600-149299000	Enhancers	Fetal Thymus	thymus
4	chr2:149295800-149298600	Enhancers	Primary hematopoietic stem cells short term culture	blood
5	chr2:149295800-149299600	Enhancers	Primary T helper cells fromperipheralblood	blood
6	chr2:149295800-149305000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
7	chr2:149296000-149299000	Enhancers	Thymus	Thymus
8	chr2:149296000-149299800	Enhancers	Primary T cells from cord blood	blood
9	chr2:149296600-149299800	Enhancers	Primary T cells fromperipheralblood	blood
10	chr2:149296800-149298000	Enhancers	Pancreas	Pancrea
11	chr2:149296800-149299800	Enhancers	Primary T killer memory cells from peripheral blood	blood
12	chr2:149296800-149303000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr2:149297000-149303400	Weak transcription	Lung	lung
14	chr2:149297400-149298600	Enhancers	Primary monocytes fromperipheralblood	blood
15	chr2:149297400-149298600	Enhancers	Primary T regulatory cells fromperipheralblood	blood
16	chr2:149297400-149299200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
17	chr2:149297600-149298400	Enhancers	Fetal Muscle Leg	muscle
18	chr2:149297600-149298400	Enhancers	GM12878-XiMat	blood
19	chr2:149297600-149298400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
20	chr2:149297600-149298600	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
21	chr2:149297600-149298600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
22	chr2:149297600-149298600	Enhancers	Spleen	Spleen
23	chr2:149297600-149298800	Enhancers	Primary B cells from cord blood	blood
24	chr2:149297600-149298800	Enhancers	Primary hematopoietic stem cells	blood
25	chr2:149297600-149298800	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
26	chr2:149297600-149299000	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
27	chr2:149297800-149298000	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr2:149297800-149298000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
29	chr2:149297800-149298200	Flanking Active TSS	Primary T helper memory cells from peripheral blood 2	blood
30	chr2:149297800-149298200	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
31	chr2:149297800-149298200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
32	chr2:149297800-149298200	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
33	chr2:149297800-149298200	Enhancers	Fetal Lung	lung
34	chr2:149297800-149298600	Enhancers	Primary B cells from peripheral blood	blood
35	chr2:149297800-149298800	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--

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