Variant report

Variant	rs2030613
Chromosome Location	chr3:142343391-142343392
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 100 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:98)

rs_ID	r²[population]
rs10935465	0.86[EUR][1000 genomes]
rs1129393	0.86[EUR][1000 genomes]
rs11715610	0.95[CHB][hapmap];0.82[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs12695767	0.83[ASN][1000 genomes]
rs12695768	0.81[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs13058771	0.81[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs13065075	0.82[EUR][1000 genomes]
rs13067795	0.84[EUR][1000 genomes]
rs13069113	0.81[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs13069307	0.82[EUR][1000 genomes]
rs13079246	0.89[CEU][hapmap];0.95[CHB][hapmap];0.82[JPT][hapmap];0.81[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs13080785	0.86[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs13085998	0.85[EUR][1000 genomes]
rs13093869	0.93[EUR][1000 genomes]
rs13099848	0.81[ASN][1000 genomes]
rs13100985	0.80[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs1357529	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1357530	1.00[CEU][hapmap];0.95[CHB][hapmap];0.86[JPT][hapmap];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs16852486	0.88[CEU][hapmap];0.95[CHB][hapmap];0.82[JPT][hapmap];0.87[ASN][1000 genomes]
rs17623267	0.81[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs1916639	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1983434	1.00[CEU][hapmap];0.95[CHB][hapmap];0.86[JPT][hapmap];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1983435	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2012010	0.81[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs2049325	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2049326	0.86[JPT][hapmap];0.97[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2140432	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2177396	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2227928	0.92[CEU][hapmap];0.81[JPT][hapmap];0.86[EUR][1000 genomes]
rs2227930	0.86[EUR][1000 genomes]
rs2354175	0.80[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs2354860	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2883380	0.88[CEU][hapmap];0.95[CHB][hapmap];0.81[JPT][hapmap];0.85[ASN][1000 genomes]
rs3736560	0.81[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs3736561	0.85[ASN][1000 genomes]
rs3922730	0.93[CEU][hapmap];0.82[JPT][hapmap]
rs4413348	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4683688	0.88[CEU][hapmap];0.93[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs4683689	0.91[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs4683690	0.89[CEU][hapmap];0.95[CHB][hapmap];0.81[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs4683691	0.82[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs6414350	0.83[EUR][1000 genomes]
rs6440088	0.86[EUR][1000 genomes]
rs6440089	0.92[CEU][hapmap];0.81[JPT][hapmap];0.86[EUR][1000 genomes]
rs6440090	0.92[EUR][1000 genomes]
rs6440091	0.89[EUR][1000 genomes]
rs6440092	0.91[EUR][1000 genomes]
rs6440093	0.92[EUR][1000 genomes]
rs6440094	0.93[CEU][hapmap];0.82[JPT][hapmap];0.92[EUR][1000 genomes]
rs6440098	1.00[CEU][hapmap];0.95[CHB][hapmap];0.86[JPT][hapmap];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6440099	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6440102	0.87[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs6768093	0.87[EUR][1000 genomes]
rs6770155	0.92[EUR][1000 genomes]
rs6775813	1.00[CEU][hapmap];0.95[CHB][hapmap];0.87[JPT][hapmap];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6780250	0.86[CEU][hapmap];0.82[JPT][hapmap]
rs6782400	0.92[CEU][hapmap];0.81[JPT][hapmap];0.86[EUR][1000 genomes]
rs6783203	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6784089	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6784361	0.81[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs6785894	0.91[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs6789958	0.88[CEU][hapmap]
rs6792259	0.93[CEU][hapmap];0.82[JPT][hapmap];1.00[YRI][hapmap];0.87[EUR][1000 genomes]
rs6793735	0.88[CEU][hapmap];0.90[CHB][hapmap];0.87[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs6797492	0.80[ASN][1000 genomes]
rs6798232	0.88[CEU][hapmap];0.95[CHB][hapmap];0.82[JPT][hapmap];0.85[ASN][1000 genomes]
rs6799752	0.93[CEU][hapmap];0.82[JPT][hapmap];1.00[YRI][hapmap];0.92[EUR][1000 genomes]
rs6802734	0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6802774	0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6808205	0.88[CEU][hapmap];0.95[CHB][hapmap];0.80[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs6808302	0.85[ASN][1000 genomes]
rs7428496	0.88[EUR][1000 genomes]
rs7430429	0.88[CEU][hapmap];0.95[CHB][hapmap];0.82[JPT][hapmap];0.80[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs7609842	0.94[AMR][1000 genomes];0.92[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7610557	0.92[CEU][hapmap];0.82[JPT][hapmap];0.92[EUR][1000 genomes]
rs7615316	1.00[CEU][hapmap];0.95[CHB][hapmap];0.87[JPT][hapmap];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7631313	1.00[CEU][hapmap];0.95[CHB][hapmap];0.86[JPT][hapmap];0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7635146	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7641330	0.82[CEU][hapmap];0.81[JPT][hapmap]
rs7646880	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7647573	0.85[EUR][1000 genomes]
rs7648354	0.94[CHB][hapmap];0.83[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs7651071	0.92[CEU][hapmap];0.81[JPT][hapmap]
rs7651542	0.84[EUR][1000 genomes]
rs940211	0.81[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs940212	0.80[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs9683085	0.85[EUR][1000 genomes]
rs9816736	0.92[CEU][hapmap];0.81[JPT][hapmap]
rs9824176	0.83[AMR][1000 genomes];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9824893	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9825207	0.87[EUR][1000 genomes]
rs9832606	0.89[CEU][hapmap];0.95[CHB][hapmap];0.82[JPT][hapmap];0.86[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs9846960	0.81[CEU][hapmap];0.81[JPT][hapmap]
rs9862919	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs9866958	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.82[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9869842	0.92[CEU][hapmap];0.81[JPT][hapmap];0.86[EUR][1000 genomes]
rs9879995	0.87[EUR][1000 genomes]
rs9882763	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][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	nsv877560	chr3:142132749-142362179	Strong transcription ZNF genes & repeats Weak transcription Active TSS Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
2	nsv932989	chr3:142204208-142423305	Weak transcription Strong transcription Active TSS Flanking Active TSS Enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:142334000-142357200	Weak transcription	Pancreas	Pancrea
2	chr3:142337800-142348400	Weak transcription	Gastric	stomach
3	chr3:142338000-142344200	Weak transcription	Colonic Mucosa	Colon
4	chr3:142338600-142343800	Weak transcription	HSMMtube	muscle
5	chr3:142340200-142345600	Weak transcription	A549	lung
6	chr3:142340600-142343400	Enhancers	Fetal Intestine Small	intestine
7	chr3:142341400-142346200	Enhancers	Pancreatic Islets	Pancreatic Islet
8	chr3:142341800-142343600	Enhancers	Stomach Mucosa	stomach
9	chr3:142342400-142345200	Active TSS	Rectal Mucosa Donor 29	rectum
10	chr3:142342600-142345000	Active TSS	Rectal Mucosa Donor 31	rectum
11	chr3:142342800-142343800	Weak transcription	Fetal Intestine Large	intestine
12	chr3:142342800-142345800	Active TSS	Duodenum Mucosa	Duodenum
13	chr3:142343200-142343400	Enhancers	Sigmoid Colon	Sigmoid Colon
14	chr3:142343200-142343800	Enhancers	Fetal Lung	lung

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