Variant report

Variant	rs7098242
Chromosome Location	chr10:18526110-18526111
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 6 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:6)

rs_ID	r²[population]
rs10828333	0.82[ASW][hapmap];1.00[CEU][hapmap];0.94[CHB][hapmap];1.00[CHD][hapmap];0.98[GIH][hapmap];1.00[JPT][hapmap];0.92[MEX][hapmap];0.90[MKK][hapmap];1.00[TSI][hapmap];0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11013126	0.88[CHB][hapmap];0.97[CHD][hapmap];0.87[MEX][hapmap];0.82[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs11013137	0.86[CHD][hapmap]
rs12359413	0.82[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs7898536	0.86[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs7920645	0.88[CHB][hapmap];0.94[CHD][hapmap];0.84[JPT][hapmap];0.82[AMR][1000 genomes];0.86[ASN][1000 genomes]

No data

Chromatin state (count:15 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:18514400-18526600	Weak transcription	Rectal Smooth Muscle	rectum
2	chr10:18515800-18532000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr10:18523000-18549400	Weak transcription	Pancreas	Pancrea
4	chr10:18523200-18529600	Weak transcription	Esophagus	oesophagus
5	chr10:18523200-18529600	Weak transcription	Left Ventricle	heart
6	chr10:18523200-18536000	Weak transcription	H1 Cell Line	embryonic stem cell
7	chr10:18523400-18529200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
8	chr10:18524400-18527200	Enhancers	Colon Smooth Muscle	Colon
9	chr10:18524600-18526200	Enhancers	Fetal Heart	heart
10	chr10:18525600-18526200	Enhancers	Right Atrium	heart
11	chr10:18525600-18526400	Weak transcription	Stomach Smooth Muscle	stomach
12	chr10:18525600-18527400	Enhancers	Ovary	ovary
13	chr10:18525800-18526200	Weak transcription	Fetal Lung	lung
14	chr10:18525800-18526800	Weak transcription	Duodenum Smooth Muscle	Duodenum
15	chr10:18526000-18532200	Weak transcription	Cortex derived primary cultured neurospheres	brain

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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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