Variant report

Variant	rs55912304
Chromosome Location	chr14:84557462-84557463
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

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

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

rs_ID	r²[population]
rs11627572	0.82[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs11628862	0.98[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs17624404	0.84[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs17657042	0.85[AFR][1000 genomes];0.85[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs17697962	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs17730419	0.85[AFR][1000 genomes];0.85[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs1779566	0.98[ASN][1000 genomes]
rs2615462	0.86[ASN][1000 genomes]
rs2787452	0.86[ASN][1000 genomes]
rs4369583	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4551972	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55645564	0.85[AFR][1000 genomes];0.85[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs72701082	0.90[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs72701083	0.90[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs72701092	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72703208	0.85[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs72703211	0.84[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs7494031	0.98[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:84550600-84558400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr14:84550600-84563800	Weak transcription	Esophagus	oesophagus
3	chr14:84556800-84557600	Enhancers	Right Atrium	heart
4	chr14:84556800-84558000	Enhancers	Ovary	ovary
5	chr14:84556800-84558600	Enhancers	Fetal Stomach	stomach
6	chr14:84556800-84558800	Enhancers	Fetal Muscle Trunk	muscle
7	chr14:84556800-84559000	Enhancers	Adipose Nuclei	Adipose
8	chr14:84557000-84558000	Enhancers	Fetal Muscle Leg	muscle
9	chr14:84557200-84558200	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
10	chr14:84557400-84558400	Weak transcription	Spleen	Spleen

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Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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