Variant report

Variant	rs1805037
Chromosome Location	chr4:26483659-26483660
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 1 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:1)

rs_ID	r²[population]
rs1800856	1.00[GIH][hapmap];1.00[MEX][hapmap];1.00[AMR][1000 genomes]

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs1805037	SEL1L3	cis	lymphoblastoid	seeQTL

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:26480200-26491000	Weak transcription	Right Atrium	heart
2	chr4:26481400-26484000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
3	chr4:26481400-26484200	Weak transcription	Muscle Satellite Cultured Cells	--
4	chr4:26481400-26484400	Weak transcription	HSMMtube	muscle
5	chr4:26481600-26484200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
6	chr4:26481600-26484200	Weak transcription	Rectal Smooth Muscle	rectum
7	chr4:26482800-26484400	Enhancers	Ovary	ovary
8	chr4:26483000-26484200	Enhancers	Colon Smooth Muscle	Colon
9	chr4:26483000-26485600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr4:26483000-26490600	Weak transcription	Gastric	stomach
11	chr4:26483200-26484200	Weak transcription	Fetal Heart	heart
12	chr4:26483600-26483800	Enhancers	Spleen	Spleen
13	chr4:26483600-26485000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
14	chr4:26483600-26486400	Enhancers	Fetal Brain Male	brain
15	chr4:26483600-26486400	Enhancers	Fetal Stomach	stomach

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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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