Variant report

Variant	rs10031415
Chromosome Location	chr4:103369480-103369481
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 4 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:4)

rs_ID	r²[population]
rs13129951	1.00[GIH][hapmap]
rs1585607	1.00[CEU][hapmap];1.00[GIH][hapmap];0.91[MEX][hapmap];1.00[TSI][hapmap]
rs7655375	0.87[CEU][hapmap]
rs7685474	1.00[CEU][hapmap];1.00[GIH][hapmap];0.91[MEX][hapmap];1.00[TSI][hapmap]

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs10031415	DDIT4L	cis	cerebellum	SCAN

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:103367800-103369600	Enhancers	Dnd41	blood
2	chr4:103368400-103370000	Enhancers	iPS-18 Cell Line	embryonic stem cell
3	chr4:103369000-103373200	Weak transcription	Primary T helper cells PMA-I stimulated	--
4	chr4:103369200-103369600	Enhancers	HUES64 Cell Line	embryonic stem cell
5	chr4:103369400-103369600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
6	chr4:103369400-103369800	Enhancers	HUES48 Cell Line	embryonic stem cell
7	chr4:103369400-103371000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
8	chr4:103369400-103373400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--

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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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