Variant report

Variant	rs60914078
Chromosome Location	chr20:13773572-13773573
allele	C/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	POLR2A	chr20:13773012-13773671	HepG2	liver:	n/a	n/a
2	JUN	chr20:13773469-13773648	K562	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr20:13765557..13767175-chr20:13773327..13775374,2	MCF-7	breast:
2	chr20:13771650..13774538-chr20:13781308..13785639,3	K562	blood:
3	chr20:13767767..13769500-chr20:13771706..13774307,2	MCF-7	breast:
4	chr20:13764475..13767391-chr20:13770944..13774600,4	K562	blood:

Variant related genes	Relation type
NDUFAF5	TF binding region
ENSG00000101247	Chromatin interaction
ENSG00000089048	Chromatin interaction

Extended variants
information (count: 16 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:8)

rs_ID	r²[population]
rs28680787	0.91[AFR][1000 genomes]
rs4813143	0.89[AFR][1000 genomes]
rs4813145	0.92[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6105169	0.90[AFR][1000 genomes]
rs6110037	0.90[AFR][1000 genomes]
rs6110048	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6110050	0.89[AFR][1000 genomes]
rs7264494	0.83[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1061303	chr20:13395546-13810990	Strong transcription Weak transcription Enhancers Genic enhancers ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv916202	chr20:13421724-14043615	Flanking Active TSS Enhancers Strong transcription Weak transcription Bivalent/Poised TSS Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
3	nsv1059817	chr20:13422602-13807968	Weak transcription Strong transcription Enhancers ZNF genes & repeats Active TSS Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	nsv1066810	chr20:13451869-14432454	Strong transcription Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
5	nsv912689	chr20:13570331-14155881	Weak transcription ZNF genes & repeats Enhancers Active TSS Flanking Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
6	nsv531478	chr20:13580524-13814797	Strong transcription Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
7	nsv1059221	chr20:13589432-13977327	Strong transcription Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
8	nsv531479	chr20:13632491-14434432	Strong transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Weak transcription Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:127 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:13766400-13793800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr20:13766400-13796800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr20:13766800-13781400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr20:13767400-13792600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr20:13767600-13775200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
6	chr20:13767600-13775200	Weak transcription	Small Intestine	intestine
7	chr20:13767600-13789800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
8	chr20:13767600-13799600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr20:13767800-13799400	Strong transcription	HUES64 Cell Line	embryonic stem cell
10	chr20:13767800-13800600	Weak transcription	Stomach Mucosa	stomach
11	chr20:13768000-13778400	Strong transcription	Fetal Muscle Leg	muscle
12	chr20:13768000-13780600	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
13	chr20:13768000-13781400	Strong transcription	Rectal Mucosa Donor 31	rectum
14	chr20:13768000-13786000	Strong transcription	iPS-20b Cell Line	embryonic stem cell
15	chr20:13768000-13794800	Strong transcription	Duodenum Mucosa	Duodenum
16	chr20:13768000-13799800	Strong transcription	Fetal Thymus	thymus
17	chr20:13768200-13776600	Strong transcription	NH-A	brain
18	chr20:13768200-13780000	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
19	chr20:13768200-13780000	Strong transcription	Placenta	Placenta
20	chr20:13768200-13780400	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr20:13768200-13799800	Strong transcription	Primary T helper cells fromperipheralblood	blood
22	chr20:13768200-13799800	Strong transcription	Monocytes-CD14+_RO01746	blood
23	chr20:13768400-13774000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
24	chr20:13768400-13799600	Strong transcription	Primary hematopoietic stem cells short term culture	blood
25	chr20:13768600-13778000	Strong transcription	Fetal Lung	lung
26	chr20:13768600-13799600	Strong transcription	HUES48 Cell Line	embryonic stem cell
27	chr20:13768800-13774600	Strong transcription	K562	blood
28	chr20:13768800-13780400	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr20:13768800-13786200	Strong transcription	HUES6 Cell Line	embryonic stem cell
30	chr20:13768800-13799600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
31	chr20:13769000-13781400	Strong transcription	Fetal Muscle Trunk	muscle
32	chr20:13769000-13799600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
33	chr20:13769200-13774000	Weak transcription	Fetal Intestine Small	intestine
34	chr20:13769200-13789800	Weak transcription	Pancreatic Islets	Pancreatic Islet
35	chr20:13769200-13799600	Strong transcription	Primary monocytes fromperipheralblood	blood
36	chr20:13769400-13775200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
37	chr20:13769400-13779800	Strong transcription	Osteobl	bone
38	chr20:13769400-13786000	Strong transcription	iPS-18 Cell Line	embryonic stem cell
39	chr20:13769400-13799400	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
40	chr20:13769400-13802000	Strong transcription	A549	lung
41	chr20:13769600-13780800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
42	chr20:13769600-13780800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
43	chr20:13769600-13799400	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
44	chr20:13769800-13773600	Strong transcription	Fetal Stomach	stomach
45	chr20:13769800-13776400	Strong transcription	Gastric	stomach
46	chr20:13769800-13778000	Strong transcription	Thymus	Thymus
47	chr20:13769800-13778400	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
48	chr20:13769800-13778400	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
49	chr20:13769800-13778600	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
50	chr20:13769800-13779200	Strong transcription	Adipose Nuclei	Adipose

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links