Variant report

Variant	rs6797842
Chromosome Location	chr3:94024808-94024809
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 65 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:50)

rs_ID	r²[population]
rs12485753	0.81[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs12630845	0.90[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs12637776	0.85[EUR][1000 genomes]
rs12638900	0.92[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs13079023	0.89[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1388637	0.92[AMR][1000 genomes];0.83[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1580098	0.90[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1584924	0.85[EUR][1000 genomes]
rs1598219	0.85[EUR][1000 genomes]
rs1598220	0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1598221	0.84[EUR][1000 genomes]
rs1598222	0.85[EUR][1000 genomes]
rs1598223	0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1598224	0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1598229	0.91[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1598230	0.90[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1598234	0.90[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1609721	0.88[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs17815906	0.92[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs2198619	0.92[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2198620	0.92[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs33970442	0.90[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs34292321	0.85[EUR][1000 genomes]
rs34430074	0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs34871190	0.87[AFR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs35067079	0.87[AFR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs35223750	0.84[AMR][1000 genomes];0.90[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs35648684	0.85[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs35797019	0.87[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs35924628	0.82[ASN][1000 genomes]
rs4241463	0.85[EUR][1000 genomes]
rs4399895	0.81[AFR][1000 genomes];0.90[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4857069	0.87[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4857070	0.85[EUR][1000 genomes]
rs4857267	0.81[ASN][1000 genomes]
rs4857270	0.80[ASN][1000 genomes]
rs4857289	0.90[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4857299	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4857300	0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs62266967	0.85[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs66612454	0.84[AMR][1000 genomes];0.82[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs66750406	0.87[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6762431	0.92[AMR][1000 genomes];0.82[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs67811013	0.92[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs71326817	0.84[AMR][1000 genomes];0.90[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7630241	0.90[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7646963	0.91[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs897184	0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs9852322	0.86[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs9855177	0.83[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:15 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv869241	chr3:93527675-94504491	Flanking Active TSS Weak transcription Strong transcription Enhancers Genic enhancers Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
2	nsv998173	chr3:93575084-94427403	Active TSS Weak transcription Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
3	nsv536644	chr3:93575084-94427403	Active TSS Enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
4	nsv1008711	chr3:93575284-94427264	Flanking Active TSS Enhancers Active TSS Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
5	nsv536646	chr3:93575284-94427264	Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Enhancers Strong transcription Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
6	nsv491829	chr3:93575285-94427263	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
7	nsv1013107	chr3:93654100-94102212	Enhancers Weak transcription Active TSS Strong transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
8	nsv536648	chr3:93654100-94102212	Weak transcription Active TSS Strong transcription Enhancers ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
9	nsv1004176	chr3:93654100-94502551	Active TSS Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
10	nsv877162	chr3:93779664-94278078	Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Weak transcription Genic enhancers Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
11	nsv877163	chr3:93795972-94047775	Weak transcription Enhancers Strong transcription ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
12	nsv1000265	chr3:94012384-94259057	Enhancers Bivalent Enhancer Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
13	nsv536650	chr3:94012384-94259057	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
14	nsv877164	chr3:94018657-94146460	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
15	nsv877165	chr3:94018657-94160736	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:37 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:94022200-94026000	Enhancers	Fetal Heart	heart
2	chr3:94022400-94025000	Enhancers	HUES6 Cell Line	embryonic stem cell
3	chr3:94022400-94026000	Enhancers	Adipose Nuclei	Adipose
4	chr3:94022600-94025200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr3:94022600-94025600	Enhancers	Rectal Smooth Muscle	rectum
6	chr3:94022600-94026000	Enhancers	Duodenum Smooth Muscle	Duodenum
7	chr3:94022800-94025000	Enhancers	Fetal Lung	lung
8	chr3:94022800-94025000	Weak transcription	Placenta	Placenta
9	chr3:94022800-94025800	Enhancers	HUES48 Cell Line	embryonic stem cell
10	chr3:94022800-94026000	Enhancers	Fetal Stomach	stomach
11	chr3:94023000-94025800	Enhancers	Colon Smooth Muscle	Colon
12	chr3:94023200-94025000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
13	chr3:94023200-94025600	Weak transcription	Brain Angular Gyrus	brain
14	chr3:94023200-94027800	Weak transcription	Brain Hippocampus Middle	brain
15	chr3:94023400-94025200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
16	chr3:94023400-94025200	Weak transcription	Fetal Brain Male	brain
17	chr3:94023400-94026000	Enhancers	Breast Myoepithelial Primary Cells	Breast
18	chr3:94023800-94026000	Enhancers	Fetal Intestine Large	intestine
19	chr3:94024000-94025000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr3:94024000-94025200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
21	chr3:94024000-94025200	Enhancers	Brain Germinal Matrix	brain
22	chr3:94024000-94025200	Weak transcription	Fetal Muscle Leg	muscle
23	chr3:94024000-94025200	Weak transcription	Ovary	ovary
24	chr3:94024000-94025200	Weak transcription	Right Atrium	heart
25	chr3:94024200-94025000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
26	chr3:94024200-94025000	Weak transcription	Brain Anterior Caudate	brain
27	chr3:94024200-94025200	Active TSS	Stomach Smooth Muscle	stomach
28	chr3:94024200-94025400	Enhancers	Fetal Brain Female	brain
29	chr3:94024200-94026200	Enhancers	iPS-15b Cell Line	embryonic stem cell
30	chr3:94024400-94025200	Weak transcription	Fetal Intestine Small	intestine
31	chr3:94024400-94026200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
32	chr3:94024600-94025200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
33	chr3:94024600-94025800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr3:94024600-94026000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
35	chr3:94024600-94026000	Enhancers	HUES64 Cell Line	embryonic stem cell
36	chr3:94024600-94026000	Enhancers	Rectal Mucosa Donor 29	rectum
37	chr3:94024800-94025000	Enhancers	HepG2	liver

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