Variant report

Variant	rs73043845
Chromosome Location	chr19:36863674-36863675
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 32 )
Associated
traits (count: 3 )

rSNPs within LD-proxies of this variant (count:29)

rs_ID	r²[population]
rs12461529	0.91[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12462725	1.00[AFR][1000 genomes];0.88[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17206379	1.00[AFR][1000 genomes];0.86[AMR][1000 genomes];0.89[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2271842	1.00[AFR][1000 genomes];0.88[AMR][1000 genomes];0.91[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2385802	0.91[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2857	0.91[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2945955	0.88[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2945956	0.88[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2945989	0.89[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2967508	0.80[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2967511	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2967516	0.84[ASN][1000 genomes]
rs2967519	0.88[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs3098393	0.89[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs3111555	0.85[ASN][1000 genomes]
rs3111556	0.89[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs3810326	1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs56378871	1.00[AFR][1000 genomes];0.86[AMR][1000 genomes];0.87[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs61706074	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62112567	0.91[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs62112568	0.91[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs62112569	0.91[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs62112624	0.90[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs62112631	1.00[AFR][1000 genomes];0.89[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62112632	1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62113869	1.00[AFR][1000 genomes];0.88[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7253122	1.00[AFR][1000 genomes];0.81[AMR][1000 genomes];0.88[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs73043902	1.00[AFR][1000 genomes];0.88[AMR][1000 genomes];0.87[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs8104241	1.00[AFR][1000 genomes];0.88[AMR][1000 genomes];0.91[EUR][1000 genomes];0.95[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	nsv2474	chr19:36804469-36865415	Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Enhancers Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
2	nsv833816	chr19:36824257-37034287	ZNF genes & repeats Active TSS Weak transcription Enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	29 gene(s)	inside rSNPs	diseases
3	nsv174	chr19:36831719-36865415	Weak transcription Strong transcription ZNF genes & repeats Active TSS Enhancers Genic enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases

mRNA abundance (count:3)

SNP	Gene	Cis/trans	Tissue	Source
rs73043845	LINC00665	cis	Nerve Tibial	GTEx
rs73043845	LINC00665	cis	Skin Sun Exposed Lower leg	GTEx
rs73043845	LINC00665	cis	Muscle Skeletal	GTEx

Chromatin state (count:67 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:36830600-36869400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr19:36832200-36868600	Weak transcription	Placenta Amnion	Placenta Amnion
3	chr19:36834200-36868800	Weak transcription	Muscle Satellite Cultured Cells	--
4	chr19:36835800-36868800	Weak transcription	H1 Cell Line	embryonic stem cell
5	chr19:36836400-36868000	Weak transcription	Psoas Muscle	Psoas
6	chr19:36838000-36868600	Weak transcription	Stomach Mucosa	stomach
7	chr19:36844200-36868800	Weak transcription	H9 Cell Line	embryonic stem cell
8	chr19:36846600-36866400	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr19:36850000-36868000	Weak transcription	Fetal Heart	heart
10	chr19:36852200-36867600	Weak transcription	HepG2	liver
11	chr19:36856600-36868400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr19:36857600-36865400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
13	chr19:36858000-36868600	Weak transcription	Brain Substantia Nigra	brain
14	chr19:36858000-36869400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr19:36858400-36868200	Weak transcription	Stomach Smooth Muscle	stomach
16	chr19:36858400-36868800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
17	chr19:36858400-36869400	Weak transcription	Left Ventricle	heart
18	chr19:36858600-36868600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
19	chr19:36858600-36868600	Weak transcription	Brain Anterior Caudate	brain
20	chr19:36858600-36869200	Weak transcription	Pancreas	Pancrea
21	chr19:36858600-36869200	Weak transcription	Right Ventricle	heart
22	chr19:36858800-36868600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
23	chr19:36859000-36865400	Weak transcription	Brain Angular Gyrus	brain
24	chr19:36859000-36865600	Weak transcription	Brain Inferior Temporal Lobe	brain
25	chr19:36859000-36865800	Weak transcription	Dnd41	blood
26	chr19:36859000-36868400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
27	chr19:36859000-36868800	Weak transcription	HUES48 Cell Line	embryonic stem cell
28	chr19:36859000-36868800	Weak transcription	HUES64 Cell Line	embryonic stem cell
29	chr19:36859000-36869000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
30	chr19:36859200-36865600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
31	chr19:36859600-36867600	Weak transcription	Colon Smooth Muscle	Colon
32	chr19:36860800-36863800	ZNF genes & repeats	Primary T helper cells PMA-I stimulated	--
33	chr19:36861000-36866000	ZNF genes & repeats	Fetal Brain Female	brain
34	chr19:36861400-36864000	Strong transcription	Fetal Lung	lung
35	chr19:36861600-36865600	Weak transcription	Brain Cingulate Gyrus	brain
36	chr19:36861600-36868800	Weak transcription	Rectal Smooth Muscle	rectum
37	chr19:36861800-36864800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
38	chr19:36861800-36865600	Weak transcription	Brain Hippocampus Middle	brain
39	chr19:36861800-36867600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
40	chr19:36861800-36867800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
41	chr19:36861800-36868000	Weak transcription	Fetal Brain Male	brain
42	chr19:36861800-36868400	Weak transcription	Ovary	ovary
43	chr19:36861800-36868600	Weak transcription	Adipose Nuclei	Adipose
44	chr19:36861800-36868600	Weak transcription	Rectal Mucosa Donor 29	rectum
45	chr19:36861800-36868600	Weak transcription	Skeletal Muscle Male	skeletal muscle
46	chr19:36861800-36868600	Weak transcription	Skeletal Muscle Female	skeletal muscle
47	chr19:36861800-36868600	Weak transcription	Thymus	Thymus
48	chr19:36861800-36868800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
49	chr19:36861800-36869000	Weak transcription	Gastric	stomach
50	chr19:36861800-36869200	Weak transcription	Aorta	Aorta

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links