Variant report

Variant	rs73396172
Chromosome Location	chr6:25330072-25330073
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 14 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs55798209	0.88[EUR][1000 genomes]
rs56000982	1.00[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56143259	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs57438642	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6929432	1.00[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6929831	1.00[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73392388	0.85[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs73392397	0.83[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs73394138	0.85[AMR][1000 genomes];0.83[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs73396160	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7758244	0.85[AMR][1000 genomes];0.83[EUR][1000 genomes];0.83[ASN][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	nsv883485	chr6:25259137-25437986	Weak transcription Enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
2	nsv883486	chr6:25260434-25422369	Weak transcription Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
3	nsv883487	chr6:25280119-25508868	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Genic enhancers 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:64 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:25306600-25331400	Weak transcription	Spleen	Spleen
2	chr6:25313800-25331400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
3	chr6:25321000-25331400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr6:25321600-25341200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
5	chr6:25323000-25333200	Weak transcription	Rectal Mucosa Donor 29	rectum
6	chr6:25324600-25330400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
7	chr6:25324600-25331600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
8	chr6:25325000-25331600	Weak transcription	Adipose Nuclei	Adipose
9	chr6:25325200-25330200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr6:25325200-25330200	Weak transcription	Esophagus	oesophagus
11	chr6:25325200-25331400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
12	chr6:25325200-25331400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr6:25325200-25331400	Weak transcription	Placenta	Placenta
14	chr6:25325200-25331400	Weak transcription	Pancreas	Pancrea
15	chr6:25325200-25331400	Weak transcription	HSMMtube	muscle
16	chr6:25325200-25336400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr6:25325200-25336400	Weak transcription	Lung	lung
18	chr6:25326800-25333000	Weak transcription	Monocytes-CD14+_RO01746	blood
19	chr6:25327000-25332600	Weak transcription	Primary monocytes fromperipheralblood	blood
20	chr6:25327400-25330200	Weak transcription	Right Atrium	heart
21	chr6:25327600-25331400	Weak transcription	Ovary	ovary
22	chr6:25327600-25332600	Weak transcription	Sigmoid Colon	Sigmoid Colon
23	chr6:25327600-25337400	Weak transcription	Brain Hippocampus Middle	brain
24	chr6:25328200-25336800	Enhancers	HUES64 Cell Line	embryonic stem cell
25	chr6:25328200-25338200	Enhancers	iPS-15b Cell Line	embryonic stem cell
26	chr6:25328400-25330200	Weak transcription	Left Ventricle	heart
27	chr6:25328400-25330400	Weak transcription	Colonic Mucosa	Colon
28	chr6:25328600-25331200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
29	chr6:25328600-25331400	Weak transcription	Stomach Mucosa	stomach
30	chr6:25328600-25331600	Weak transcription	Fetal Brain Female	brain
31	chr6:25328600-25333000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
32	chr6:25328800-25331200	Weak transcription	Rectal Mucosa Donor 31	rectum
33	chr6:25329000-25336000	Enhancers	HUES48 Cell Line	embryonic stem cell
34	chr6:25329200-25330600	Enhancers	iPS-18 Cell Line	embryonic stem cell
35	chr6:25329200-25332200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr6:25329400-25330200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr6:25329400-25330400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
38	chr6:25329400-25330400	Enhancers	Brain Anterior Caudate	brain
39	chr6:25329400-25330600	Enhancers	Aorta	Aorta
40	chr6:25329400-25332000	Enhancers	Fetal Intestine Small	intestine
41	chr6:25329400-25332400	Enhancers	Small Intestine	intestine
42	chr6:25329400-25336200	Enhancers	HUES6 Cell Line	embryonic stem cell
43	chr6:25329400-25336400	Enhancers	iPS-20b Cell Line	embryonic stem cell
44	chr6:25329600-25330200	Enhancers	ES-I3 Cell Line	embryonic stem cell
45	chr6:25329600-25330400	Enhancers	H9 Cell Line	embryonic stem cell
46	chr6:25329600-25330400	Enhancers	Brain Substantia Nigra	brain
47	chr6:25329600-25330400	Enhancers	Duodenum Mucosa	Duodenum
48	chr6:25329600-25330400	Enhancers	Fetal Lung	lung
49	chr6:25329600-25330600	Enhancers	Gastric	stomach
50	chr6:25329600-25330800	Enhancers	Fetal Intestine Large	intestine

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