Variant report

Variant	rs537957307
Chromosome Location	chr1:172155664-172155665
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 2 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1000079	chr1:172146935-172230545	Flanking Active TSS Enhancers Active TSS Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
2	esv3331688	chr1:172155645-172155926	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:172150800-172159000	Enhancers	Primary B cells from peripheral blood	blood
2	chr1:172151000-172160800	Weak transcription	Brain Cingulate Gyrus	brain
3	chr1:172152800-172156000	Enhancers	Fetal Muscle Leg	muscle
4	chr1:172153200-172157800	Enhancers	Primary B cells from cord blood	blood
5	chr1:172153400-172155800	Enhancers	Fetal Stomach	stomach
6	chr1:172153800-172155800	Enhancers	HUES48 Cell Line	embryonic stem cell
7	chr1:172153800-172156200	Enhancers	Fetal Kidney	kidney
8	chr1:172154000-172156000	Enhancers	Primary T regulatory cells fromperipheralblood	blood
9	chr1:172154000-172161000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
10	chr1:172154800-172158200	Weak transcription	Brain Hippocampus Middle	brain
11	chr1:172155000-172156000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
12	chr1:172155200-172156200	Weak transcription	Primary T cells from cord blood	blood
13	chr1:172155400-172158400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
14	chr1:172155600-172156200	Enhancers	GM12878-XiMat	blood

Quick Search:

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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