Variant report

Variant	rs8026600
Chromosome Location	chr15:72615409-72615410
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr15:72615312..72618236-chr15:72766595..72769031,2	MCF-7	breast:
2	chr15:72614594..72616097-chr15:72631711..72633732,2	K562	blood:

Variant related genes	Relation type
ENSG00000166233	Chromatin interaction
ENSG00000261423	Chromatin interaction

Extended variants
information (count: 43 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:40)

rs_ID	r²[population]
rs11072353	0.88[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11072355	0.82[ASN][1000 genomes]
rs11072356	0.80[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11072357	1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11629508	0.81[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11631113	0.88[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11635828	0.98[ASN][1000 genomes]
rs11636289	0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11637797	0.90[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12440927	0.82[ASN][1000 genomes]
rs12591975	0.81[ASN][1000 genomes]
rs12911449	0.91[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs12914971	0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2162235	0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2278150	0.88[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2288258	0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs28712686	0.98[AFR][1000 genomes]
rs2912205	0.87[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs2912220	0.81[AFR][1000 genomes]
rs2912221	0.98[AFR][1000 genomes]
rs2912223	1.00[AFR][1000 genomes]
rs2912226	0.91[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs2912229	0.91[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs2959915	0.82[ASN][1000 genomes]
rs2959922	0.90[AFR][1000 genomes]
rs2959925	0.98[AFR][1000 genomes]
rs2959926	0.98[AFR][1000 genomes]
rs2959938	0.85[AFR][1000 genomes];0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs3087652	0.81[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs35949555	0.80[ASN][1000 genomes]
rs4606667	0.90[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4776591	1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4777498	0.88[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs55792138	0.99[AFR][1000 genomes];0.89[AMR][1000 genomes];0.86[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs59353578	0.88[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs61481811	0.80[ASN][1000 genomes]
rs6495000	0.90[AFR][1000 genomes];0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs73438486	0.81[ASN][1000 genomes]
rs8025332	0.81[ASN][1000 genomes]
rs9672916	0.98[AFR][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	nsv431395	chr15:72266174-72701777	Strong transcription Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	144 gene(s)	inside rSNPs	diseases
2	nsv530817	chr15:72350885-72773374	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	173 gene(s)	inside rSNPs	diseases
3	esv3430860	chr15:72373723-72849907	Weak transcription ZNF genes & repeats Flanking Active TSS Enhancers Active TSS Genic enhancers Bivalent Enhancer Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	172 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:80 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:72609800-72624800	Weak transcription	HepG2	liver
2	chr15:72612800-72618600	Weak transcription	Aorta	Aorta
3	chr15:72613000-72618000	Weak transcription	Psoas Muscle	Psoas
4	chr15:72613000-72618400	Weak transcription	Left Ventricle	heart
5	chr15:72613000-72618600	Weak transcription	Lung	lung
6	chr15:72613000-72619200	Weak transcription	Colon Smooth Muscle	Colon
7	chr15:72613000-72631600	Weak transcription	Right Atrium	heart
8	chr15:72613000-72636000	Weak transcription	Right Ventricle	heart
9	chr15:72613000-72636400	Weak transcription	Gastric	stomach
10	chr15:72613000-72637000	Weak transcription	Colonic Mucosa	Colon
11	chr15:72613200-72615800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr15:72613200-72615800	Weak transcription	Brain Substantia Nigra	brain
13	chr15:72613200-72616600	Weak transcription	Liver	Liver
14	chr15:72613200-72618400	Weak transcription	Adipose Nuclei	Adipose
15	chr15:72613200-72618400	Weak transcription	Brain Hippocampus Middle	brain
16	chr15:72613200-72618600	Weak transcription	Stomach Smooth Muscle	stomach
17	chr15:72613200-72618800	Weak transcription	Fetal Intestine Large	intestine
18	chr15:72613200-72619200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
19	chr15:72613200-72619200	Weak transcription	Fetal Muscle Trunk	muscle
20	chr15:72613200-72619400	Weak transcription	Fetal Stomach	stomach
21	chr15:72613200-72630600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
22	chr15:72613200-72630600	Weak transcription	Rectal Smooth Muscle	rectum
23	chr15:72613200-72630800	Weak transcription	Muscle Satellite Cultured Cells	--
24	chr15:72613200-72631600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
25	chr15:72613200-72633000	Weak transcription	Thymus	Thymus
26	chr15:72613200-72633600	Weak transcription	Brain Inferior Temporal Lobe	brain
27	chr15:72613200-72634200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
28	chr15:72613200-72635600	Weak transcription	Placenta Amnion	Placenta Amnion
29	chr15:72613200-72635800	Weak transcription	Pancreas	Pancrea
30	chr15:72613200-72636000	Weak transcription	Rectal Mucosa Donor 31	rectum
31	chr15:72613200-72636200	Weak transcription	HSMMtube	muscle
32	chr15:72613200-72651000	Weak transcription	Stomach Mucosa	stomach
33	chr15:72613200-72666800	Weak transcription	Fetal Heart	heart
34	chr15:72613400-72615600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
35	chr15:72613400-72616000	Weak transcription	Primary neutrophils fromperipheralblood	blood
36	chr15:72613400-72616200	Weak transcription	Fetal Lung	lung
37	chr15:72613400-72616400	Weak transcription	Primary B cells from cord blood	blood
38	chr15:72613400-72618200	Weak transcription	Duodenum Smooth Muscle	Duodenum
39	chr15:72613400-72618400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
40	chr15:72613400-72618400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
41	chr15:72613400-72618400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
42	chr15:72613400-72618400	Weak transcription	Monocytes-CD14+_RO01746	blood
43	chr15:72613400-72618600	Weak transcription	Sigmoid Colon	Sigmoid Colon
44	chr15:72613400-72619200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
45	chr15:72613400-72619200	Weak transcription	Placenta	Placenta
46	chr15:72613400-72620600	Weak transcription	Small Intestine	intestine
47	chr15:72613400-72623000	Weak transcription	Brain Cingulate Gyrus	brain
48	chr15:72613400-72623600	Weak transcription	NHLF	lung
49	chr15:72613400-72627400	Weak transcription	NHDF-Ad	bronchial
50	chr15:72613400-72629200	Weak transcription	Brain Anterior Caudate	brain

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links