Variant report

Variant	rs10737519
Chromosome Location	chr1:165821328-165821329
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr1:165819266..165822080-chr1:165829077..165831771,2	MCF-7	breast:
2	chr1:165795645..165798284-chr1:165816849..165821681,5	MCF-7	breast:
3	chr1:165818712..165822734-chr1:165823086..165826851,4	MCF-7	breast:

Variant related genes	Relation type
ENSG00000143183	Chromatin interaction
ENSG00000143179	Chromatin interaction

Extended variants
information (count: 26 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:22)

rs_ID	r²[population]
rs10753694	0.80[AMR][1000 genomes];0.86[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10800162	0.82[AMR][1000 genomes];0.87[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10918291	0.91[ASN][1000 genomes]
rs10918294	0.85[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11590711	0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1934275	0.91[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2185268	0.94[AMR][1000 genomes];0.81[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs34800847	0.99[ASN][1000 genomes]
rs4483381	0.89[ASN][1000 genomes]
rs4535982	0.93[AMR][1000 genomes];0.85[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4548416	0.96[ASN][1000 genomes]
rs4657481	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6426941	0.82[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs6677965	0.96[ASN][1000 genomes]
rs6678380	0.96[ASN][1000 genomes]
rs6682894	0.94[ASN][1000 genomes]
rs6684773	0.93[ASN][1000 genomes]
rs6686237	0.88[ASN][1000 genomes]
rs6690966	0.80[AMR][1000 genomes];0.86[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6702462	0.87[AMR][1000 genomes];0.80[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7517175	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7539793	0.89[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2756102	chr1:165652342-165877342	Weak transcription Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	48 gene(s)	inside rSNPs	diseases
2	esv2830094	chr1:165785503-165840411	Flanking Active TSS Enhancers Weak transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	31 gene(s)	inside rSNPs	diseases
3	nsv548097	chr1:165797966-165825166	Flanking Active TSS Active TSS Weak transcription Enhancers Strong transcription 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	23 gene(s)	inside rSNPs	diseases
4	esv2755529	chr1:165813862-165858354	Weak transcription Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:94 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:165812200-165823200	Weak transcription	Aorta	Aorta
2	chr1:165812200-165823200	Weak transcription	Fetal Stomach	stomach
3	chr1:165812200-165823400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr1:165812400-165821800	Weak transcription	H9 Cell Line	embryonic stem cell
5	chr1:165812400-165822200	Weak transcription	HUES6 Cell Line	embryonic stem cell
6	chr1:165812400-165823200	Weak transcription	Left Ventricle	heart
7	chr1:165812400-165823200	Weak transcription	Right Ventricle	heart
8	chr1:165812400-165823200	Weak transcription	Sigmoid Colon	Sigmoid Colon
9	chr1:165812600-165821800	Weak transcription	Pancreatic Islets	Pancreatic Islet
10	chr1:165813000-165821800	Weak transcription	NHLF	lung
11	chr1:165813000-165823200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
12	chr1:165813800-165821800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
13	chr1:165814000-165822000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr1:165814000-165823200	Weak transcription	Small Intestine	intestine
15	chr1:165814400-165821800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
16	chr1:165816200-165825000	Weak transcription	Rectal Mucosa Donor 29	rectum
17	chr1:165817600-165823800	Enhancers	Fetal Thymus	thymus
18	chr1:165818000-165821800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
19	chr1:165818000-165829200	Enhancers	Primary monocytes fromperipheralblood	blood
20	chr1:165818400-165821400	Enhancers	Breast Myoepithelial Primary Cells	Breast
21	chr1:165818400-165821400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
22	chr1:165818400-165823800	Enhancers	Thymus	Thymus
23	chr1:165818600-165823200	Weak transcription	Fetal Muscle Leg	muscle
24	chr1:165818600-165828000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
25	chr1:165818800-165823400	Weak transcription	Right Atrium	heart
26	chr1:165818800-165824800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
27	chr1:165818800-165826600	Weak transcription	Esophagus	oesophagus
28	chr1:165819000-165822000	Weak transcription	HepG2	liver
29	chr1:165819000-165823200	Weak transcription	Adipose Nuclei	Adipose
30	chr1:165819000-165826000	Weak transcription	Brain Hippocampus Middle	brain
31	chr1:165819000-165826200	Weak transcription	Stomach Mucosa	stomach
32	chr1:165819200-165823000	Weak transcription	Hela-S3	cervix
33	chr1:165819200-165824600	Weak transcription	Rectal Mucosa Donor 31	rectum
34	chr1:165819200-165824800	Weak transcription	Brain Inferior Temporal Lobe	brain
35	chr1:165819400-165821400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
36	chr1:165819400-165821600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
37	chr1:165819400-165822400	Weak transcription	Skeletal Muscle Male	skeletal muscle
38	chr1:165819600-165824400	Enhancers	HMEC	breast
39	chr1:165820200-165821400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
40	chr1:165820200-165821400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
41	chr1:165820200-165821400	Flanking Active TSS	Dnd41	blood
42	chr1:165820200-165822000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
43	chr1:165820200-165822200	Enhancers	Primary hematopoietic stem cells	blood
44	chr1:165820200-165822400	Enhancers	Psoas Muscle	Psoas
45	chr1:165820200-165825800	Enhancers	iPS-20b Cell Line	embryonic stem cell
46	chr1:165820400-165821600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
47	chr1:165820400-165822400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
48	chr1:165820400-165825200	Enhancers	Fetal Heart	heart
49	chr1:165820400-165827600	Enhancers	iPS-18 Cell Line	embryonic stem cell
50	chr1:165820600-165822000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung

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