Variant report

Variant	rs10521299
Chromosome Location	chr17:15144179-15144180
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr17:15142573..15145462-chr17:15150924..15153034,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TEKT3-1	chr17:15143744-15147713	ENSG00000265308.1

Extended variants
information (count: 9 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:5)

rs_ID	r²[population]
rs3785648	1.00[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs3785651	1.00[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs3785652	1.00[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs56857955	1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7415	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	nsv1066329	chr17:14983674-15294071	Weak transcription Enhancers Flanking Active TSS Genic enhancers Bivalent Enhancer Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	22 gene(s)	inside rSNPs	diseases
2	nsv543212	chr17:14983674-15294071	Active TSS Genic enhancers Enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	22 gene(s)	inside rSNPs	diseases
3	nsv492304	chr17:15043353-15611753	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	58 gene(s)	inside rSNPs	diseases
4	nsv916652	chr17:15093600-15856310	Strong transcription Weak transcription Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	73 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:72 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:15131600-15145600	Strong transcription	Fetal Muscle Trunk	muscle
2	chr17:15132200-15144400	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
3	chr17:15132200-15158800	Weak transcription	Hela-S3	cervix
4	chr17:15134400-15151000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
5	chr17:15135200-15144800	Genic enhancers	Colon Smooth Muscle	Colon
6	chr17:15135800-15151200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr17:15135800-15160200	Weak transcription	Pancreas	Pancrea
8	chr17:15137000-15151200	Weak transcription	Fetal Intestine Small	intestine
9	chr17:15137200-15158000	Weak transcription	Stomach Mucosa	stomach
10	chr17:15138000-15144200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
11	chr17:15138600-15144200	Enhancers	Primary monocytes fromperipheralblood	blood
12	chr17:15139000-15152800	Weak transcription	Colonic Mucosa	Colon
13	chr17:15139800-15148400	Weak transcription	Right Atrium	heart
14	chr17:15139800-15151200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr17:15139800-15160200	Weak transcription	HUES6 Cell Line	embryonic stem cell
16	chr17:15140000-15145800	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
17	chr17:15140200-15147800	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
18	chr17:15140200-15151000	Weak transcription	HMEC	breast
19	chr17:15141400-15144200	Strong transcription	Fetal Stomach	stomach
20	chr17:15141600-15144200	Genic enhancers	Left Ventricle	heart
21	chr17:15142000-15146200	Strong transcription	A549	lung
22	chr17:15142400-15145000	Genic enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
23	chr17:15142600-15144600	Enhancers	Fetal Heart	heart
24	chr17:15142600-15144600	Enhancers	K562	blood
25	chr17:15142600-15145400	Genic enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
26	chr17:15142600-15154000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
27	chr17:15142600-15159000	Weak transcription	Fetal Kidney	kidney
28	chr17:15142600-15159000	Weak transcription	NH-A	brain
29	chr17:15142800-15159200	Weak transcription	Fetal Brain Male	brain
30	chr17:15143000-15144800	Enhancers	Skeletal Muscle Male	skeletal muscle
31	chr17:15143000-15145400	Enhancers	Skeletal Muscle Female	skeletal muscle
32	chr17:15143000-15147800	Weak transcription	Brain Inferior Temporal Lobe	brain
33	chr17:15143000-15148200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
34	chr17:15143000-15148400	Weak transcription	Spleen	Spleen
35	chr17:15143000-15150800	Weak transcription	Duodenum Mucosa	Duodenum
36	chr17:15143000-15150800	Weak transcription	NHLF	lung
37	chr17:15143000-15151000	Weak transcription	Rectal Mucosa Donor 29	rectum
38	chr17:15143000-15151200	Weak transcription	Muscle Satellite Cultured Cells	--
39	chr17:15143000-15151200	Weak transcription	Cortex derived primary cultured neurospheres	brain
40	chr17:15143000-15151200	Weak transcription	Osteobl	bone
41	chr17:15143000-15151400	Weak transcription	HUVEC	blood vessel
42	chr17:15143000-15152400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
43	chr17:15143000-15152400	Weak transcription	Rectal Mucosa Donor 31	rectum
44	chr17:15143000-15154000	Weak transcription	Sigmoid Colon	Sigmoid Colon
45	chr17:15143000-15156800	Weak transcription	Gastric	stomach
46	chr17:15143200-15144400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
47	chr17:15143200-15146400	Strong transcription	Adipose Nuclei	Adipose
48	chr17:15143200-15147400	Weak transcription	Fetal Lung	lung
49	chr17:15143200-15148400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
50	chr17:15143200-15151000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain

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