Variant report

Variant	rs8011917
Chromosome Location	chr14:69085934-69085935
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	chr14:69043397..69045562-chr14:69085788..69088006,2	MCF-7	breast:
2	chr14:69085914..69087953-chr14:69091172..69093355,2	K562	blood:

Extended variants
information (count: 18 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:18)

rs_ID	r²[population]
rs10131921	0.82[ASN][1000 genomes]
rs10143415	0.87[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17106015	0.91[ASN][1000 genomes]
rs17106039	0.89[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17106049	1.00[ASN][1000 genomes]
rs2331779	0.82[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2877493	0.82[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61224239	0.92[ASN][1000 genomes]
rs61987066	0.92[ASN][1000 genomes]
rs61987069	1.00[AFR][1000 genomes];0.87[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs61987070	0.92[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs61987071	0.92[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs61987100	0.91[ASN][1000 genomes]
rs72729562	0.91[ASN][1000 genomes]
rs8007479	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8009151	1.00[ASN][1000 genomes]
rs8009865	0.92[ASN][1000 genomes]
rs8014901	1.00[ASN][1000 genomes]

No data

Chromatin state (count:21 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:69083800-69086200	Weak transcription	Fetal Heart	heart
2	chr14:69084800-69088200	Weak transcription	Brain Inferior Temporal Lobe	brain
3	chr14:69084800-69088200	Weak transcription	Colon Smooth Muscle	Colon
4	chr14:69085000-69086600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
5	chr14:69085000-69087800	Enhancers	HepG2	liver
6	chr14:69085200-69086400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
7	chr14:69085200-69088200	Weak transcription	Primary T cells from cord blood	blood
8	chr14:69085400-69086400	Enhancers	Skeletal Muscle Male	skeletal muscle
9	chr14:69085400-69089000	Enhancers	Placenta	Placenta
10	chr14:69085400-69095200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr14:69085600-69086600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr14:69085600-69088000	Enhancers	K562	blood
13	chr14:69085800-69086000	Weak transcription	Fetal Intestine Small	intestine
14	chr14:69085800-69086200	Weak transcription	Fetal Muscle Leg	muscle
15	chr14:69085800-69086200	Weak transcription	HSMMtube	muscle
16	chr14:69085800-69086400	Enhancers	Skeletal Muscle Female	skeletal muscle
17	chr14:69085800-69086400	Weak transcription	HSMM	muscle
18	chr14:69085800-69086600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
19	chr14:69085800-69086600	Weak transcription	Left Ventricle	heart
20	chr14:69085800-69088000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
21	chr14:69085800-69091000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin

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