Variant report

Variant	rs7649225
Chromosome Location	chr3:142792759-142792760
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr3:142791929..142795122-chr3:142795804..142797960,4	K562	blood:
2	chr3:142791929..142795122-chr3:142795804..142798158,4	K562	blood:

Extended variants
information (count: 96 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:90)

rs_ID	r²[population]
rs10413	0.81[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs1043898	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs10451867	0.92[EUR][1000 genomes]
rs10513184	0.91[EUR][1000 genomes]
rs1053950	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs10790	0.87[EUR][1000 genomes]
rs10935475	0.86[EUR][1000 genomes]
rs10935479	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs11915462	0.88[EUR][1000 genomes]
rs11922201	0.84[EUR][1000 genomes]
rs12485790	0.81[EUR][1000 genomes]
rs12490776	0.92[EUR][1000 genomes]
rs12492904	0.87[EUR][1000 genomes]
rs12695770	0.81[EUR][1000 genomes]
rs13075955	0.92[EUR][1000 genomes]
rs13088422	0.81[EUR][1000 genomes]
rs13094293	0.84[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs13099995	0.82[EUR][1000 genomes]
rs1349262	0.80[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs13715	0.90[EUR][1000 genomes]
rs1375814	0.89[EUR][1000 genomes]
rs1449868	0.90[EUR][1000 genomes]
rs1449869	0.93[EUR][1000 genomes]
rs1530753	0.93[EUR][1000 genomes]
rs1532588	0.89[EUR][1000 genomes]
rs1545597	0.82[EUR][1000 genomes]
rs17557029	0.87[EUR][1000 genomes]
rs1814565	0.84[EUR][1000 genomes]
rs1827159	0.93[EUR][1000 genomes]
rs1839406	0.90[EUR][1000 genomes]
rs1868569	0.89[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs1868570	0.89[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs1965343	0.89[EUR][1000 genomes]
rs2045306	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs2124541	0.89[EUR][1000 genomes]
rs2124542	0.86[EUR][1000 genomes]
rs2124543	0.86[EUR][1000 genomes]
rs2137586	0.86[EUR][1000 genomes]
rs2175739	0.86[EUR][1000 genomes]
rs2290549	0.84[EUR][1000 genomes]
rs2353408	0.93[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs2353409	0.93[EUR][1000 genomes]
rs2353411	0.80[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs3821645	0.93[EUR][1000 genomes]
rs3856697	0.87[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs3902877	0.87[EUR][1000 genomes]
rs4030582	0.89[EUR][1000 genomes]
rs4683444	0.80[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs4683721	0.87[EUR][1000 genomes]
rs4683722	0.90[EUR][1000 genomes]
rs4683723	0.88[EUR][1000 genomes]
rs4683724	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs56382522	0.85[EUR][1000 genomes]
rs6440129	0.89[EUR][1000 genomes]
rs6440131	0.93[EUR][1000 genomes]
rs6440132	0.91[EUR][1000 genomes]
rs6440133	0.84[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs6440134	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs6770102	0.86[EUR][1000 genomes]
rs6778454	0.86[EUR][1000 genomes]
rs6781080	0.90[EUR][1000 genomes]
rs6781887	0.89[EUR][1000 genomes]
rs6783145	0.90[EUR][1000 genomes]
rs6784200	0.81[EUR][1000 genomes]
rs6796771	0.81[EUR][1000 genomes]
rs6805417	0.93[EUR][1000 genomes]
rs6806551	0.92[EUR][1000 genomes]
rs6808406	0.81[EUR][1000 genomes]
rs6808689	0.90[EUR][1000 genomes]
rs7611721	0.90[EUR][1000 genomes]
rs7623532	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs7644475	0.81[EUR][1000 genomes]
rs7648143	0.84[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs7652745	0.88[EUR][1000 genomes]
rs766360	0.84[EUR][1000 genomes]
rs936194	0.80[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs936196	0.80[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs936197	0.92[EUR][1000 genomes]
rs937498	0.87[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs9814656	0.87[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs9816317	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs9820175	0.80[EUR][1000 genomes]
rs9831162	0.81[EUR][1000 genomes]
rs9835348	0.90[EUR][1000 genomes]
rs9847059	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs9851353	0.89[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs9862433	0.90[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs9875210	0.82[EUR][1000 genomes]
rs9877128	0.93[EUR][1000 genomes]
rs9877135	0.93[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv877562	chr3:142573789-142846370	Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Enhancers Weak transcription Bivalent Enhancer Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
2	esv2757893	chr3:142720230-142962932	Enhancers Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
3	esv2759183	chr3:142720230-142964373	Strong transcription Weak transcription Enhancers Bivalent Enhancer Active TSS Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
4	nsv591921	chr3:142762487-142841740	Bivalent/Poised TSS Active TSS Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Bivalent Enhancer ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases
5	nsv1004467	chr3:142768867-142800605	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS	Chromatin interactive region miRNA target site	2 gene(s)	inside rSNPs	diseases
6	nsv1004682	chr3:142768867-142804154	Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region lncRNA miRNA target site	4 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs7649225	SR140	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:142775600-142794400	Weak transcription	Duodenum Smooth Muscle	Duodenum
2	chr3:142789800-142794000	Enhancers	K562	blood
3	chr3:142790800-142796400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr3:142791200-142792800	Enhancers	HUES6 Cell Line	embryonic stem cell
5	chr3:142792200-142793400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
6	chr3:142792400-142793400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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