Variant report

Variant	rs10024625
Chromosome Location	chr4:7876331-7876332
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

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

rSNPs within LD-proxies of this variant (count:34)

rs_ID	r²[population]
rs10005650	0.96[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs28425587	0.81[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs28434072	0.92[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs28498817	0.86[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs28607438	0.90[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs28668205	0.90[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs28675899	0.88[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs28735181	0.90[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs28735634	0.90[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs28842326	0.90[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs4401450	0.90[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs4478172	0.83[ASN][1000 genomes]
rs4488938	0.82[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs4696771	0.90[ASN][1000 genomes]
rs61081420	0.90[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs61214925	0.90[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs6605361	0.90[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs6820041	0.92[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs6839086	0.87[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs6842743	0.90[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs71175434	0.90[AMR][1000 genomes]
rs73073924	0.84[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs73073939	0.90[ASN][1000 genomes]
rs73088591	0.86[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs73088594	0.88[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs73090508	0.90[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs73090513	0.90[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs73090514	0.90[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs7376703	0.90[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs7676488	0.90[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs7691757	0.92[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs7695510	0.88[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs9330346	0.90[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs9654093	0.85[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv491712	chr4:7582506-8155069	Enhancers Bivalent Enhancer Genic enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
2	esv34140	chr4:7787936-8172491	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats 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	18 gene(s)	inside rSNPs	diseases
3	esv2754386	chr4:7822449-7992909	Weak transcription Enhancers Active TSS Genic enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	esv2756298	chr4:7822449-7992909	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
5	nsv878578	chr4:7841833-7969594	Enhancers Flanking Active TSS Genic enhancers Weak transcription ZNF genes & repeats Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:86 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:7857800-7896400	Weak transcription	Spleen	Spleen
2	chr4:7866000-7877600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
3	chr4:7866000-7877800	Weak transcription	HepG2	liver
4	chr4:7866000-7882400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
5	chr4:7866000-7885600	Weak transcription	Esophagus	oesophagus
6	chr4:7869200-7880800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
7	chr4:7869600-7877600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
8	chr4:7869800-7878000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
9	chr4:7870400-7876800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
10	chr4:7870400-7879200	Weak transcription	Duodenum Mucosa	Duodenum
11	chr4:7870400-7882400	Weak transcription	HUES48 Cell Line	embryonic stem cell
12	chr4:7870600-7877200	Weak transcription	Primary T cells fromperipheralblood	blood
13	chr4:7870600-7877200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
14	chr4:7870600-7877600	Weak transcription	Primary T helper cells fromperipheralblood	blood
15	chr4:7870600-7878000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
16	chr4:7870600-7878000	Weak transcription	Rectal Mucosa Donor 29	rectum
17	chr4:7873400-7877200	Weak transcription	Primary T cells from cord blood	blood
18	chr4:7873400-7878800	Weak transcription	Fetal Intestine Small	intestine
19	chr4:7873400-7879000	Weak transcription	H1 Cell Line	embryonic stem cell
20	chr4:7873400-7880000	Weak transcription	Lung	lung
21	chr4:7873400-7883000	Weak transcription	Right Ventricle	heart
22	chr4:7873600-7878000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
23	chr4:7873600-7878200	Weak transcription	H9 Cell Line	embryonic stem cell
24	chr4:7873600-7894000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
25	chr4:7873800-7878200	Weak transcription	Fetal Intestine Large	intestine
26	chr4:7874200-7877800	Weak transcription	Ovary	ovary
27	chr4:7874400-7877800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
28	chr4:7874400-7878000	Weak transcription	Fetal Kidney	kidney
29	chr4:7874400-7878000	Weak transcription	Left Ventricle	heart
30	chr4:7874400-7878200	Weak transcription	Brain Cingulate Gyrus	brain
31	chr4:7874400-7878600	Weak transcription	Fetal Brain Female	brain
32	chr4:7874400-7880200	Weak transcription	Gastric	stomach
33	chr4:7874400-7880200	Weak transcription	Rectal Mucosa Donor 31	rectum
34	chr4:7874400-7880800	Weak transcription	Pancreas	Pancrea
35	chr4:7874600-7876800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
36	chr4:7874600-7877400	Weak transcription	Fetal Heart	heart
37	chr4:7874600-7877400	Weak transcription	NH-A	brain
38	chr4:7874600-7877600	Weak transcription	HUVEC	blood vessel
39	chr4:7874600-7877800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
40	chr4:7874600-7877800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
41	chr4:7874600-7877800	Weak transcription	Placenta	Placenta
42	chr4:7874600-7877800	Weak transcription	Fetal Stomach	stomach
43	chr4:7874600-7877800	Weak transcription	Rectal Smooth Muscle	rectum
44	chr4:7874600-7877800	Weak transcription	Stomach Smooth Muscle	stomach
45	chr4:7874600-7877800	Weak transcription	NHLF	lung
46	chr4:7874600-7878000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
47	chr4:7874600-7878000	Weak transcription	Aorta	Aorta
48	chr4:7874600-7878000	Weak transcription	Psoas Muscle	Psoas
49	chr4:7874600-7878000	Weak transcription	Right Atrium	heart
50	chr4:7874600-7878200	Weak transcription	Brain Germinal Matrix	brain

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