Variant report

Variant	rs73802824
Chromosome Location	chr4:22479735-22479736
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	MAFF	chr4:22479442-22479763	HepG2	liver:	n/a	n/a
2	MAFK	chr4:22479435-22479771	HepG2	liver:	n/a	chr4:22479594-22479609 chr4:22479594-22479605 chr4:22479594-22479605 chr4:22479594-22479610 chr4:22479593-22479607
3	MAFK	chr4:22479473-22479756	HepG2	liver:	n/a	chr4:22479594-22479609 chr4:22479594-22479605 chr4:22479594-22479605 chr4:22479594-22479610 chr4:22479593-22479607
4	MAFK	chr4:22479443-22479763	IMR90	lung:	n/a	chr4:22479594-22479609 chr4:22479594-22479605 chr4:22479594-22479605 chr4:22479594-22479610 chr4:22479593-22479607

Variant related genes	Relation type
GPR125	TF binding region

Extended variants
information (count: 39 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:36)

rs_ID	r²[population]
rs11932316	1.00[AMR][1000 genomes]
rs56029242	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs56383378	0.96[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs56965161	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs57310135	0.92[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs58098085	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59383860	1.00[EUR][1000 genomes]
rs61574687	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs61588486	0.85[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs61793366	0.89[AFR][1000 genomes]
rs61793367	0.89[AFR][1000 genomes]
rs6812519	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73800932	1.00[EUR][1000 genomes]
rs73800934	1.00[EUR][1000 genomes]
rs73800935	1.00[EUR][1000 genomes]
rs73800940	1.00[EUR][1000 genomes]
rs73800946	1.00[EUR][1000 genomes]
rs73800949	1.00[EUR][1000 genomes]
rs73800956	1.00[EUR][1000 genomes]
rs73800958	0.85[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs73800959	0.85[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs73800963	0.89[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs73800964	0.92[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs73802816	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73802817	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73802819	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73802821	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73802827	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs73802829	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73802830	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73802831	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73802832	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73802835	1.00[AMR][1000 genomes]
rs73802836	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7666836	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7666972	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3349061	chr4:22379581-22887563	Enhancers Weak transcription Strong transcription Active TSS Genic enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
2	nsv878752	chr4:22414023-22501043	Enhancers Flanking Active TSS Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
3	nsv821634	chr4:22427074-22865948	Enhancers Weak transcription Active TSS Strong transcription Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:65 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:22420600-22488000	Weak transcription	Aorta	Aorta
2	chr4:22450400-22484000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
3	chr4:22450400-22493200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr4:22456800-22485000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
5	chr4:22462000-22493200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr4:22462400-22483600	Weak transcription	Liver	Liver
7	chr4:22466600-22484000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr4:22472200-22480200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
9	chr4:22472600-22484200	Weak transcription	Sigmoid Colon	Sigmoid Colon
10	chr4:22472600-22484400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr4:22472600-22486200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
12	chr4:22472800-22482400	Weak transcription	Ovary	ovary
13	chr4:22473000-22482400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
14	chr4:22473200-22487400	Weak transcription	Right Ventricle	heart
15	chr4:22473400-22484400	Weak transcription	Fetal Muscle Trunk	muscle
16	chr4:22473600-22484200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
17	chr4:22474000-22483200	Weak transcription	Fetal Brain Female	brain
18	chr4:22474200-22484000	Weak transcription	Primary hematopoietic stem cells	blood
19	chr4:22474200-22486200	Weak transcription	Fetal Stomach	stomach
20	chr4:22474400-22484200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
21	chr4:22474400-22484400	Weak transcription	Skeletal Muscle Male	skeletal muscle
22	chr4:22474600-22482400	Weak transcription	Rectal Smooth Muscle	rectum
23	chr4:22474600-22484200	Weak transcription	HSMMtube	muscle
24	chr4:22474800-22482000	Weak transcription	Fetal Muscle Leg	muscle
25	chr4:22475000-22480000	Weak transcription	Primary T cells from cord blood	blood
26	chr4:22475000-22484000	Weak transcription	Left Ventricle	heart
27	chr4:22475000-22484800	Weak transcription	Fetal Intestine Large	intestine
28	chr4:22475000-22489400	Weak transcription	Lung	lung
29	chr4:22475200-22480000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
30	chr4:22475200-22482400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr4:22475200-22484200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
32	chr4:22475200-22486000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
33	chr4:22476600-22482600	Weak transcription	H1 Cell Line	embryonic stem cell
34	chr4:22476600-22484400	Weak transcription	Psoas Muscle	Psoas
35	chr4:22476600-22485200	Weak transcription	Skeletal Muscle Female	skeletal muscle
36	chr4:22476600-22487200	Weak transcription	Small Intestine	intestine
37	chr4:22476800-22481800	Weak transcription	HUES64 Cell Line	embryonic stem cell
38	chr4:22477000-22481400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
39	chr4:22477000-22482400	Weak transcription	HUES48 Cell Line	embryonic stem cell
40	chr4:22477000-22482400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
41	chr4:22477000-22482400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
42	chr4:22477000-22482800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
43	chr4:22477000-22484600	Weak transcription	Hela-S3	cervix
44	chr4:22477000-22484800	Weak transcription	Duodenum Smooth Muscle	Duodenum
45	chr4:22477000-22485000	Weak transcription	A549	lung
46	chr4:22477200-22482200	Weak transcription	HMEC	breast
47	chr4:22477200-22482400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
48	chr4:22477200-22484400	Weak transcription	Pancreas	Pancrea
49	chr4:22477600-22482400	Weak transcription	NHEK	skin
50	chr4:22477800-22482400	Weak transcription	Fetal Heart	heart

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