Variant report

Variant	rs7688218
Chromosome Location	chr4:79203835-79203836
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 55 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:49)

rs_ID	r²[population]
rs17003090	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs17003102	0.87[AMR][1000 genomes]
rs17003104	0.87[AMR][1000 genomes]
rs17003105	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs17003106	0.85[AMR][1000 genomes]
rs17003107	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs17003109	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1825417	0.87[AMR][1000 genomes]
rs41391850	0.87[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs55714031	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs55895609	0.87[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs56323989	0.85[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs58723665	0.86[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs59429199	0.86[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs59522692	0.87[AMR][1000 genomes]
rs61150533	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs61476761	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6812049	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6821829	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6822437	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6834011	0.95[AFR][1000 genomes];0.87[AMR][1000 genomes]
rs6838026	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6839334	0.87[AMR][1000 genomes]
rs6840763	0.87[AMR][1000 genomes]
rs6855248	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs728200	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73827911	0.85[AMR][1000 genomes]
rs73827912	0.87[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs73827913	0.87[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs73827916	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73827918	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73827922	0.87[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs73827923	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73827925	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73827930	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73827931	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73827932	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73827934	0.87[AMR][1000 genomes]
rs73827935	0.87[AMR][1000 genomes]
rs73827943	0.87[AMR][1000 genomes]
rs73827946	0.85[AMR][1000 genomes]
rs73827948	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7667557	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7682296	0.87[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs7687027	0.87[AMR][1000 genomes]
rs7687406	0.87[AMR][1000 genomes]
rs7690232	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7699637	0.87[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs994186	0.87[AMR][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	nsv534024	chr4:78785189-79437403	ZNF genes & repeats Flanking Active TSS Enhancers Active TSS Weak transcription Strong transcription Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
2	nsv1009633	chr4:78887573-79652236	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
3	nsv525530	chr4:79024524-79266563	Enhancers Weak transcription ZNF genes & repeats Genic enhancers Strong transcription Flanking Active TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
4	nsv1010782	chr4:79057839-79387207	Weak transcription Enhancers Strong transcription ZNF genes & repeats Genic enhancers Flanking Active TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
5	nsv829978	chr4:79144453-79291868	Strong transcription Weak transcription Enhancers ZNF genes & repeats Genic enhancers Flanking Active TSS Bivalent Enhancer Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
6	nsv818246	chr4:79184338-79221851	Enhancers Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Active TSS Genic enhancers Bivalent Enhancer	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	chr4:79169800-79213800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
2	chr4:79174800-79214400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr4:79187600-79214800	Weak transcription	Left Ventricle	heart
4	chr4:79187800-79210400	Weak transcription	Fetal Kidney	kidney
5	chr4:79188000-79209400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr4:79188600-79218400	Weak transcription	Aorta	Aorta
7	chr4:79189400-79207400	Weak transcription	Fetal Lung	lung
8	chr4:79191400-79213600	Weak transcription	Psoas Muscle	Psoas
9	chr4:79192200-79213800	Weak transcription	Fetal Heart	heart
10	chr4:79198200-79214000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chr4:79198400-79212400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
12	chr4:79198600-79206200	Weak transcription	Fetal Intestine Small	intestine
13	chr4:79198600-79207000	Weak transcription	Fetal Intestine Large	intestine
14	chr4:79198600-79207600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr4:79198600-79207600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr4:79198600-79215600	Weak transcription	Esophagus	oesophagus
17	chr4:79198600-79217600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
18	chr4:79198600-79220200	Weak transcription	Pancreas	Pancrea
19	chr4:79198600-79221000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
20	chr4:79198600-79241400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr4:79198800-79213800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
22	chr4:79199800-79207400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
23	chr4:79200600-79205600	Weak transcription	H9 Cell Line	embryonic stem cell
24	chr4:79200600-79213600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
25	chr4:79200600-79213800	Weak transcription	Skeletal Muscle Female	skeletal muscle
26	chr4:79201400-79204000	Weak transcription	H1 Cell Line	embryonic stem cell
27	chr4:79201600-79205400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
28	chr4:79203000-79204000	Enhancers	ES-I3 Cell Line	embryonic stem cell
29	chr4:79203400-79204200	Strong transcription	HepG2	liver
30	chr4:79203600-79211600	Strong transcription	HUES48 Cell Line	embryonic stem cell
31	chr4:79203800-79204000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr4:79203800-79204200	Strong transcription	iPS-18 Cell Line	embryonic stem cell
33	chr4:79203800-79205200	Weak transcription	HUES6 Cell Line	embryonic stem cell
34	chr4:79203800-79206800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
35	chr4:79203800-79210600	Strong transcription	HUES64 Cell Line	embryonic stem cell
36	chr4:79203800-79211000	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
37	chr4:79203800-79211400	Strong transcription	iPS-20b Cell Line	embryonic stem cell

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