Variant report

Variant	rs73345891
Chromosome Location	chr8:125727673-125727674
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr8:125724601..125726380-chr8:125726742..125729212,2	MCF-7	breast:
2	chr8:125723226..125726139-chr8:125726907..125728669,2	K562	blood:

Extended variants
information (count: 15 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs10505444	1.00[EUR][1000 genomes]
rs28810782	1.00[EUR][1000 genomes]
rs56350078	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs57679308	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs57692957	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs58327286	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73345821	1.00[EUR][1000 genomes]
rs73345837	1.00[EUR][1000 genomes]
rs73345871	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73345875	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73345878	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73345889	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73707003	1.00[EUR][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	nsv891434	chr8:125630655-126324432	Strong transcription Enhancers Weak transcription Active TSS Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	80 gene(s)	inside rSNPs	diseases
2	nsv1016502	chr8:125657664-125845074	Weak transcription Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	19 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:70 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:125702600-125730800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
2	chr8:125721600-125728000	Weak transcription	HUES6 Cell Line	embryonic stem cell
3	chr8:125721600-125728000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
4	chr8:125721600-125729200	Weak transcription	Fetal Kidney	kidney
5	chr8:125722200-125730600	Weak transcription	Fetal Stomach	stomach
6	chr8:125722200-125732200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
7	chr8:125722400-125728000	Weak transcription	Gastric	stomach
8	chr8:125722400-125728200	Weak transcription	Rectal Mucosa Donor 29	rectum
9	chr8:125722400-125729000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr8:125722600-125728200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr8:125722600-125730800	Weak transcription	Duodenum Smooth Muscle	Duodenum
12	chr8:125722600-125732600	Weak transcription	Primary T helper cells fromperipheralblood	blood
13	chr8:125723000-125730200	Weak transcription	Sigmoid Colon	Sigmoid Colon
14	chr8:125723200-125728000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
15	chr8:125723200-125730000	Weak transcription	Fetal Lung	lung
16	chr8:125723200-125737200	Weak transcription	Colon Smooth Muscle	Colon
17	chr8:125723400-125728200	Weak transcription	Brain Anterior Caudate	brain
18	chr8:125723600-125728200	Weak transcription	Placenta	Placenta
19	chr8:125723600-125737200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr8:125723800-125728000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
21	chr8:125723800-125728400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
22	chr8:125723800-125730800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
23	chr8:125724000-125728000	Weak transcription	Brain Inferior Temporal Lobe	brain
24	chr8:125724000-125728200	Weak transcription	Brain Angular Gyrus	brain
25	chr8:125724000-125730000	Weak transcription	Brain Hippocampus Middle	brain
26	chr8:125724600-125728000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
27	chr8:125724600-125732400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr8:125724600-125732400	Weak transcription	Esophagus	oesophagus
29	chr8:125724600-125738200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
30	chr8:125724800-125727800	Weak transcription	Fetal Heart	heart
31	chr8:125724800-125727800	Weak transcription	Lung	lung
32	chr8:125724800-125728200	Weak transcription	Skeletal Muscle Male	skeletal muscle
33	chr8:125724800-125730400	Weak transcription	Fetal Muscle Trunk	muscle
34	chr8:125724800-125737400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
35	chr8:125725000-125728000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
36	chr8:125725000-125730200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr8:125725200-125728200	Weak transcription	Fetal Brain Male	brain
38	chr8:125725200-125730000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
39	chr8:125725200-125730200	Weak transcription	Fetal Brain Female	brain
40	chr8:125725400-125729200	Enhancers	Brain Germinal Matrix	brain
41	chr8:125725600-125728000	Weak transcription	Cortex derived primary cultured neurospheres	brain
42	chr8:125725600-125735200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
43	chr8:125725800-125728200	Enhancers	Primary monocytes fromperipheralblood	blood
44	chr8:125725800-125729000	Enhancers	Skeletal Muscle Female	skeletal muscle
45	chr8:125726000-125728800	Enhancers	Spleen	Spleen
46	chr8:125726200-125728000	Enhancers	Monocytes-CD14+_RO01746	blood
47	chr8:125726200-125732400	Enhancers	HepG2	liver
48	chr8:125726400-125727800	Enhancers	Fetal Intestine Small	intestine
49	chr8:125726400-125728000	Enhancers	Primary B cells from cord blood	blood
50	chr8:125726600-125727800	Weak transcription	Right Ventricle	heart

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links