Variant report

Variant	rs7772242
Chromosome Location	chr6:15796710-15796711
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	chr6:15788511..15792316-chr6:15794070..15797091,4	K562	blood:
2	chr6:15793143..15797186-chr6:15800762..15804369,3	K562	blood:

Extended variants
information (count: 34 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:34)

rs_ID	r²[population]
rs11751763	1.00[ASN][1000 genomes]
rs11753586	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs13199464	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs16876746	1.00[ASN][1000 genomes]
rs1927582	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1927583	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1927584	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2181435	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs2206341	1.00[ASN][1000 genomes]
rs34030405	1.00[ASN][1000 genomes]
rs34080473	1.00[ASN][1000 genomes]
rs34669273	1.00[ASN][1000 genomes]
rs35110594	1.00[ASN][1000 genomes]
rs35835933	1.00[ASN][1000 genomes]
rs36212519	1.00[ASN][1000 genomes]
rs41413446	1.00[CEU][hapmap];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs443804	1.00[CEU][hapmap];0.83[EUR][1000 genomes]
rs4605871	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55638296	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55974491	1.00[ASN][1000 genomes]
rs56135160	1.00[ASN][1000 genomes]
rs56170994	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56213329	1.00[ASN][1000 genomes]
rs56328138	1.00[ASN][1000 genomes]
rs6459413	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs6913914	1.00[CEU][hapmap];1.00[CHB][hapmap];0.82[YRI][hapmap];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6914558	1.00[ASN][1000 genomes]
rs6918979	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs72823461	1.00[ASN][1000 genomes]
rs73724483	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7738190	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs7739825	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs7760793	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs7776332	1.00[ASN][1000 genomes]

No data

Chromatin state (count:17 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:15791000-15798000	Enhancers	Fetal Muscle Leg	muscle
2	chr6:15793200-15797600	Enhancers	Fetal Heart	heart
3	chr6:15793800-15796800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
4	chr6:15794400-15796800	Weak transcription	HMEC	breast
5	chr6:15795400-15796800	Enhancers	Primary monocytes fromperipheralblood	blood
6	chr6:15795400-15797600	Enhancers	HSMMtube	muscle
7	chr6:15796000-15797800	Enhancers	Psoas Muscle	Psoas
8	chr6:15796400-15797000	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
9	chr6:15796400-15797200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
10	chr6:15796400-15797400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr6:15796400-15797400	Enhancers	Left Ventricle	heart
12	chr6:15796400-15797400	Enhancers	Right Atrium	heart
13	chr6:15796400-15797400	Enhancers	Right Ventricle	heart
14	chr6:15796400-15798000	Enhancers	Placenta	Placenta
15	chr6:15796600-15796800	Enhancers	Aorta	Aorta
16	chr6:15796600-15796800	Active TSS	Monocytes-CD14+_RO01746	blood
17	chr6:15796600-15797000	Enhancers	Skeletal Muscle Male	skeletal muscle

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