Variant report

Variant	rs2921326
Chromosome Location	chr11:70707736-70707737
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 10 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs10751308	0.83[EUR][1000 genomes]
rs11237722	0.91[CEU][hapmap];0.85[TSI][hapmap];0.86[EUR][1000 genomes]
rs1207273	0.86[ASN][1000 genomes]
rs12806832	0.86[CEU][hapmap];0.83[EUR][1000 genomes]
rs17161143	0.93[YRI][hapmap]
rs3017478	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs3017479	0.83[EUR][1000 genomes]
rs3019837	0.87[EUR][1000 genomes]
rs517114	0.91[CEU][hapmap];0.89[CHB][hapmap];0.90[JPT][hapmap];0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6592814	0.83[EUR][1000 genomes]

No data

Chromatin state (count:18 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:70670000-70731800	Weak transcription	Gastric	stomach
2	chr11:70698600-70709000	Weak transcription	Fetal Intestine Small	intestine
3	chr11:70699800-70709800	Weak transcription	Fetal Brain Male	brain
4	chr11:70700000-70708000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr11:70701000-70712200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr11:70701800-70722800	Weak transcription	Pancreas	Pancrea
7	chr11:70702200-70724000	Weak transcription	Liver	Liver
8	chr11:70704600-70707800	Weak transcription	Fetal Muscle Leg	muscle
9	chr11:70706400-70708200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr11:70706600-70708400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr11:70706600-70724400	Weak transcription	HepG2	liver
12	chr11:70706800-70708400	Enhancers	iPS-18 Cell Line	embryonic stem cell
13	chr11:70707000-70708600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
14	chr11:70707200-70707800	Enhancers	HUES64 Cell Line	embryonic stem cell
15	chr11:70707200-70708200	Enhancers	HUES48 Cell Line	embryonic stem cell
16	chr11:70707200-70708400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
17	chr11:70707200-70708800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr11:70707400-70735200	Weak transcription	Fetal Intestine Large	intestine

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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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