Variant report

Variant	rs6775813
Chromosome Location	chr3:142345623-142345624
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr3:142340189..142342403-chr3:142344376..142347027,3	K562	blood:
2	chr3:142343680..142345636-chr3:142364474..142366774,2	K562	blood:
3	chr3:142344136..142346877-chr3:142364474..142366213,2	K562	blood:

Variant related genes	Relation type
ENSG00000120756	Chromatin interaction

Extended variants
information (count: 102 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:100)

rs_ID	r²[population]
rs10935465	0.86[EUR][1000 genomes]
rs1129393	0.86[EUR][1000 genomes]
rs11715610	1.00[CHB][hapmap];0.81[JPT][hapmap];0.94[ASN][1000 genomes]
rs12695767	0.81[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs12695768	0.86[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs13058771	0.86[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs13065075	0.82[EUR][1000 genomes]
rs13067795	0.84[EUR][1000 genomes]
rs13069113	0.86[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs13069307	0.82[EUR][1000 genomes]
rs13079246	0.89[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.86[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs13080785	0.91[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs13085998	0.84[EUR][1000 genomes]
rs13093869	0.93[EUR][1000 genomes]
rs13099848	0.90[ASN][1000 genomes]
rs13100985	0.85[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs1357529	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1357530	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs16852486	0.88[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.83[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs17623267	0.86[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs1916639	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1983434	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1983435	0.85[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2012010	0.86[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs2030613	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]
rs2049325	1.00[CEU][hapmap];0.90[CHB][hapmap];0.86[JPT][hapmap];0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2049326	0.81[CHB][hapmap];0.80[JPT][hapmap];0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2140432	1.00[CEU][hapmap];0.95[CHB][hapmap];0.86[JPT][hapmap];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2177396	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2227928	0.92[CEU][hapmap];0.86[EUR][1000 genomes]
rs2227930	0.86[EUR][1000 genomes]
rs2354175	0.85[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs2354860	0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2883380	0.88[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.83[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs3736560	0.86[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs3736561	0.83[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs3922730	0.93[CEU][hapmap]
rs4413348	1.00[CEU][hapmap];0.90[CHB][hapmap];0.86[JPT][hapmap];0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4683688	0.88[CEU][hapmap];0.88[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs4683689	0.86[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs4683690	0.89[CEU][hapmap];1.00[CHB][hapmap];0.91[JPT][hapmap];0.86[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs4683691	0.91[ASN][1000 genomes]
rs6414350	0.83[EUR][1000 genomes]
rs6440088	0.86[EUR][1000 genomes]
rs6440089	0.92[CEU][hapmap];0.86[EUR][1000 genomes]
rs6440090	0.91[EUR][1000 genomes]
rs6440091	0.88[EUR][1000 genomes]
rs6440092	0.90[EUR][1000 genomes]
rs6440093	0.92[EUR][1000 genomes]
rs6440094	0.93[CEU][hapmap];0.92[EUR][1000 genomes]
rs6440098	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6440099	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6440101	0.85[YRI][hapmap]
rs6440102	0.82[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs6768093	0.87[EUR][1000 genomes]
rs6770155	0.91[EUR][1000 genomes]
rs6780250	0.86[CEU][hapmap]
rs6782400	0.92[CEU][hapmap];0.85[EUR][1000 genomes]
rs6783203	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6784089	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6784361	0.86[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs6785894	0.86[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs6789958	0.88[CEU][hapmap]
rs6792259	0.93[CEU][hapmap];0.86[EUR][1000 genomes]
rs6793735	0.88[CEU][hapmap];0.95[CHB][hapmap];0.90[JPT][hapmap];0.82[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs6797492	0.89[ASN][1000 genomes]
rs6798232	0.88[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.84[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs6799752	0.93[CEU][hapmap];0.91[EUR][1000 genomes]
rs6802734	0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6802774	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6808205	0.88[CEU][hapmap];1.00[CHB][hapmap];0.90[JPT][hapmap];0.85[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs6808302	0.82[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs7428496	0.88[EUR][1000 genomes]
rs7430429	0.88[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.85[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs7609842	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7610557	0.92[CEU][hapmap];0.91[EUR][1000 genomes]
rs7615316	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7631313	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.80[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7635146	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7641330	0.82[CEU][hapmap]
rs7646880	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7647573	0.84[EUR][1000 genomes]
rs7648354	1.00[CHB][hapmap];0.91[ASN][1000 genomes]
rs7651071	0.92[CEU][hapmap]
rs7651542	0.84[EUR][1000 genomes]
rs940211	0.86[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs940212	0.85[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs9683085	0.84[EUR][1000 genomes]
rs9816377	0.87[YRI][hapmap]
rs9816736	0.92[CEU][hapmap]
rs9824176	0.87[AMR][1000 genomes];0.94[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs9824893	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs9825207	0.87[EUR][1000 genomes]
rs9832606	0.89[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.84[YRI][hapmap];0.91[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs9846960	0.81[CEU][hapmap]
rs9862919	1.00[CEU][hapmap];0.90[CHB][hapmap];0.86[JPT][hapmap]
rs9866958	1.00[CEU][hapmap];0.95[CHB][hapmap];0.87[JPT][hapmap];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs9869842	0.92[CEU][hapmap];0.86[EUR][1000 genomes]
rs9879995	0.87[EUR][1000 genomes]
rs9882763	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.86[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:12 , 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	chr3:142341400-142346200	Enhancers	Pancreatic Islets	Pancreatic Islet
4	chr3:142342800-142345800	Active TSS	Duodenum Mucosa	Duodenum
5	chr3:142343400-142348600	Weak transcription	Sigmoid Colon	Sigmoid Colon
6	chr3:142343400-142366400	Weak transcription	Fetal Intestine Small	intestine
7	chr3:142344800-142346600	Enhancers	K562	blood
8	chr3:142345000-142346000	Enhancers	Stomach Mucosa	stomach
9	chr3:142345200-142353800	Weak transcription	Rectal Mucosa Donor 29	rectum
10	chr3:142345600-142345800	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
11	chr3:142345600-142346200	Enhancers	A549	lung
12	chr3:142345600-142346200	Enhancers	HepG2	liver

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