Variant report

Variant	rs6783736
Chromosome Location	chr3:141474970-141474971
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr3:141462837..141465084-chr3:141474852..141476857,2	K562	blood:
2	chr3:141466931..141469705-chr3:141473220..141475379,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000114125	Chromatin interaction

Extended variants
information (count: 34 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:33)

rs_ID	r²[population]
rs11542226	0.85[EUR][1000 genomes]
rs1533501	0.80[EUR][1000 genomes]
rs16851704	0.88[EUR][1000 genomes]
rs16851717	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16851740	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16851752	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1879284	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1879285	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1980192	0.84[AFR][1000 genomes];0.88[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs3773840	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4538350	0.84[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4588340	0.80[EUR][1000 genomes]
rs57394236	0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs57805567	0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs57983026	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs58115387	0.85[EUR][1000 genomes]
rs58300294	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs59998648	0.88[EUR][1000 genomes]
rs60938827	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61278509	0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs61294533	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs61632965	0.88[EUR][1000 genomes]
rs6783647	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73872318	0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs73872319	0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs73872322	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs73872326	0.82[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs7632069	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7642922	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7643689	0.85[EUR][1000 genomes]
rs9789959	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9789973	0.90[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9790075	0.88[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv949709	chr3:141295050-142178144	Weak transcription Strong transcription Flanking Active TSS Enhancers Genic enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	61 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs6783736	RNF7	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:25 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:141461800-141498200	Weak transcription	Right Ventricle	heart
2	chr3:141465000-141481400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
3	chr3:141466200-141475800	Weak transcription	Psoas Muscle	Psoas
4	chr3:141466600-141475200	Weak transcription	Esophagus	oesophagus
5	chr3:141467000-141477000	Weak transcription	Muscle Satellite Cultured Cells	--
6	chr3:141467000-141481600	Weak transcription	Lung	lung
7	chr3:141467000-141483400	Weak transcription	Fetal Lung	lung
8	chr3:141467200-141475200	Weak transcription	Fetal Brain Female	brain
9	chr3:141467200-141475800	Weak transcription	Primary T cells from cord blood	blood
10	chr3:141467400-141476000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
11	chr3:141470000-141481400	Weak transcription	Rectal Mucosa Donor 31	rectum
12	chr3:141470000-141481600	Weak transcription	Placenta	Placenta
13	chr3:141470000-141482600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
14	chr3:141470000-141483400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr3:141470000-141483400	Weak transcription	Primary hematopoietic stem cells	blood
16	chr3:141470000-141483400	Weak transcription	Fetal Stomach	stomach
17	chr3:141470000-141483600	Weak transcription	Primary monocytes fromperipheralblood	blood
18	chr3:141470000-141486400	Weak transcription	Brain Hippocampus Middle	brain
19	chr3:141470400-141482200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
20	chr3:141470800-141483400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr3:141471200-141475600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
22	chr3:141471600-141483600	Weak transcription	Fetal Thymus	thymus
23	chr3:141471800-141483600	Weak transcription	Monocytes-CD14+_RO01746	blood
24	chr3:141472000-141500800	Weak transcription	Thymus	Thymus
25	chr3:141472600-141484800	Weak transcription	Breast Myoepithelial Primary Cells	Breast

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