Variant report

Variant	rs72675239
Chromosome Location	chr14:35093244-35093245
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr14:35090867..35093292-chr14:35095702..35100762,5	MCF-7	breast:
2	chr14:35089260..35092373-chr14:35092594..35095994,3	MCF-7	breast:
3	chr14:35062591..35065493-chr14:35091107..35093912,2	K562	blood:
4	chr14:35091495..35095564-chr14:35101048..35103200,4	MCF-7	breast:
5	chr14:35087584..35096037-chr14:35096409..35100819,12	MCF-7	breast:
6	chr14:35089053..35090728-chr14:35092071..35094626,3	MCF-7	breast:
7	chr14:35090354..35093574-chr14:35095898..35099059,4	K562	blood:

Variant related genes	Relation type
ENSG00000129515	Chromatin interaction

Extended variants
information (count: 24 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:15)

rs_ID	r²[population]
rs56310586	0.87[AMR][1000 genomes]
rs58909728	0.95[EUR][1000 genomes]
rs60183626	0.82[EUR][1000 genomes]
rs67163867	0.82[EUR][1000 genomes]
rs72673460	0.90[EUR][1000 genomes]
rs72673462	0.90[EUR][1000 genomes]
rs72673463	0.82[EUR][1000 genomes]
rs72673478	0.82[EUR][1000 genomes]
rs72675213	0.95[EUR][1000 genomes]
rs72675222	0.95[EUR][1000 genomes]
rs72675225	1.00[AFR][1000 genomes];0.95[EUR][1000 genomes]
rs72675227	0.95[EUR][1000 genomes]
rs72675230	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72675232	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72675270	0.87[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1040980	chr14:34345018-35255592	Strong transcription Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	109 gene(s)	inside rSNPs	diseases
2	nsv1048408	chr14:34958352-35255592	Weak transcription Strong transcription Flanking Active TSS Active TSS Enhancers Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	63 gene(s)	inside rSNPs	diseases
3	esv3392700	chr14:34989406-35365530	Enhancers Genic enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS 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	85 gene(s)	inside rSNPs	diseases
4	nsv1040303	chr14:35040853-35101044	Enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
5	nsv542027	chr14:35040853-35101044	Weak transcription Strong transcription Active TSS Enhancers Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
6	nsv1038360	chr14:35040853-35152886	Strong transcription Weak transcription Enhancers Genic enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
7	esv3408652	chr14:35069966-35110821	Strong transcription Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
8	nsv523334	chr14:35075022-35131862	Flanking Active TSS Strong transcription Active TSS Enhancers Weak transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
9	nsv1041857	chr14:35084889-35417180	Strong transcription Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	45 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:125 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:35054600-35098400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr14:35060800-35097800	Weak transcription	Pancreatic Islets	Pancreatic Islet
3	chr14:35063000-35098400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr14:35068400-35098000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
5	chr14:35070400-35098600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr14:35073600-35097800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
7	chr14:35076600-35098000	Weak transcription	HSMMtube	muscle
8	chr14:35077000-35093400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
9	chr14:35077000-35097600	Weak transcription	Esophagus	oesophagus
10	chr14:35077000-35098600	Weak transcription	Pancreas	Pancrea
11	chr14:35077600-35097800	Weak transcription	Skeletal Muscle Male	skeletal muscle
12	chr14:35077600-35098000	Weak transcription	Aorta	Aorta
13	chr14:35077600-35098200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
14	chr14:35077600-35098600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
15	chr14:35078000-35098000	Weak transcription	H9 Cell Line	embryonic stem cell
16	chr14:35078000-35098000	Weak transcription	Placenta Amnion	Placenta Amnion
17	chr14:35078000-35098200	Weak transcription	Ovary	ovary
18	chr14:35078200-35098600	Weak transcription	Gastric	stomach
19	chr14:35079400-35097800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr14:35081200-35095200	Strong transcription	Fetal Muscle Leg	muscle
21	chr14:35081200-35097000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
22	chr14:35081600-35093800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
23	chr14:35082200-35094400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
24	chr14:35085400-35097800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr14:35085600-35098000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
26	chr14:35086000-35095800	Strong transcription	HepG2	liver
27	chr14:35086200-35097600	Weak transcription	Lung	lung
28	chr14:35087800-35095400	Strong transcription	Fetal Muscle Trunk	muscle
29	chr14:35088800-35095400	Strong transcription	Primary B cells from peripheral blood	blood
30	chr14:35089000-35094200	Strong transcription	Fetal Intestine Large	intestine
31	chr14:35089200-35093800	Strong transcription	HSMM	muscle
32	chr14:35089200-35094600	Strong transcription	HUES64 Cell Line	embryonic stem cell
33	chr14:35089400-35095200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
34	chr14:35089400-35097200	Weak transcription	Right Ventricle	heart
35	chr14:35089600-35093600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr14:35089600-35095200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
37	chr14:35089600-35097600	Weak transcription	Stomach Mucosa	stomach
38	chr14:35089600-35098000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
39	chr14:35089800-35097600	Weak transcription	Colonic Mucosa	Colon
40	chr14:35090400-35094200	Strong transcription	Primary B cells from cord blood	blood
41	chr14:35090400-35097600	Weak transcription	Spleen	Spleen
42	chr14:35090600-35094200	Strong transcription	HUES6 Cell Line	embryonic stem cell
43	chr14:35090600-35094200	Strong transcription	Primary T cells from cord blood	blood
44	chr14:35090600-35094600	Strong transcription	Sigmoid Colon	Sigmoid Colon
45	chr14:35090600-35096200	Strong transcription	Placenta	Placenta
46	chr14:35091000-35094600	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
47	chr14:35091000-35095800	Weak transcription	Fetal Heart	heart
48	chr14:35091000-35096000	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
49	chr14:35091000-35097000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
50	chr14:35091000-35097800	Weak transcription	Fetal Lung	lung

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