Variant report

Variant	rs61596558
Chromosome Location	chr15:78342787-78342788
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	chr15:78333663..78335514-chr15:78341566..78343908,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TBC1D2B-4	chr15:78342467-78345090	ucscGeneNc_uc002bfo_2

Extended variants
information (count: 12 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs11858138	0.85[AFR][1000 genomes];0.89[AMR][1000 genomes]
rs16953970	1.00[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs16969397	0.89[AMR][1000 genomes]
rs16969464	0.89[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs57993009	0.89[AMR][1000 genomes]
rs58416217	0.89[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs59499270	0.89[AMR][1000 genomes]
rs60031052	0.81[EUR][1000 genomes]
rs61183047	0.89[AMR][1000 genomes]
rs735663	0.91[AFR][1000 genomes];0.89[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv529491	chr15:77932659-78751516	Genic enhancers Bivalent Enhancer Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	80 gene(s)	inside rSNPs	diseases
2	nsv1051558	chr15:78315542-78364947	Strong transcription Flanking Active TSS Weak transcription Enhancers Genic enhancers Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:126 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:78296200-78358200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
2	chr15:78309200-78354200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
3	chr15:78317000-78344400	Weak transcription	H1 Cell Line	embryonic stem cell
4	chr15:78317800-78344400	Weak transcription	H9 Cell Line	embryonic stem cell
5	chr15:78317800-78344400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
6	chr15:78321200-78343800	Weak transcription	NHEK	skin
7	chr15:78327600-78351400	Weak transcription	Pancreatic Islets	Pancreatic Islet
8	chr15:78330600-78342800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
9	chr15:78331200-78344400	Weak transcription	Psoas Muscle	Psoas
10	chr15:78331400-78348600	Weak transcription	A549	lung
11	chr15:78331600-78348600	Weak transcription	K562	blood
12	chr15:78332800-78343000	Weak transcription	Hela-S3	cervix
13	chr15:78336600-78344400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
14	chr15:78337000-78347800	Weak transcription	Ovary	ovary
15	chr15:78337200-78342800	Weak transcription	HUES64 Cell Line	embryonic stem cell
16	chr15:78337200-78344400	Enhancers	Primary T helper cells fromperipheralblood	blood
17	chr15:78337800-78344600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
18	chr15:78338200-78344400	Enhancers	Rectal Mucosa Donor 31	rectum
19	chr15:78338600-78345400	Enhancers	Duodenum Mucosa	Duodenum
20	chr15:78338800-78344600	Enhancers	Primary monocytes fromperipheralblood	blood
21	chr15:78338800-78344800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
22	chr15:78338800-78347000	Genic enhancers	Fetal Thymus	thymus
23	chr15:78339000-78342800	Enhancers	Brain Inferior Temporal Lobe	brain
24	chr15:78339000-78342800	Enhancers	Spleen	Spleen
25	chr15:78339000-78343600	Enhancers	NHDF-Ad	bronchial
26	chr15:78339000-78344800	Enhancers	Colon Smooth Muscle	Colon
27	chr15:78339000-78345000	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
28	chr15:78339000-78345000	Enhancers	Small Intestine	intestine
29	chr15:78339000-78345200	Genic enhancers	Fetal Stomach	stomach
30	chr15:78339000-78345400	Enhancers	Primary B cells from cord blood	blood
31	chr15:78339000-78346400	Enhancers	Skeletal Muscle Female	skeletal muscle
32	chr15:78339200-78343400	Enhancers	NHLF	lung
33	chr15:78339200-78344800	Enhancers	Brain Angular Gyrus	brain
34	chr15:78339200-78344800	Enhancers	Duodenum Smooth Muscle	Duodenum
35	chr15:78339400-78344600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
36	chr15:78339600-78343400	Enhancers	Skeletal Muscle Male	skeletal muscle
37	chr15:78339800-78343200	Enhancers	Fetal Muscle Leg	muscle
38	chr15:78339800-78343800	Enhancers	HUVEC	blood vessel
39	chr15:78340000-78343600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
40	chr15:78340000-78343600	Enhancers	Fetal Kidney	kidney
41	chr15:78340000-78343800	Enhancers	Cortex derived primary cultured neurospheres	brain
42	chr15:78340000-78345200	Enhancers	Right Atrium	heart
43	chr15:78340000-78345200	Enhancers	NH-A	brain
44	chr15:78340200-78344800	Enhancers	Brain Hippocampus Middle	brain
45	chr15:78340400-78344000	Weak transcription	HepG2	liver
46	chr15:78340600-78343600	Enhancers	Placenta Amnion	Placenta Amnion
47	chr15:78340600-78343800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
48	chr15:78340600-78344400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
49	chr15:78340800-78344400	Weak transcription	Gastric	stomach
50	chr15:78340800-78346200	Genic enhancers	Liver	Liver

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