Variant report

Variant	rs188093157
Chromosome Location	chr3:50723436-50723437
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 1 )
Associated
traits (count: 0)

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3396836	chr3:50723339-50723677	Weak transcription	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:50713200-50727600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr3:50714600-50725000	Weak transcription	Pancreatic Islets	Pancreatic Islet
3	chr3:50715200-50724800	Weak transcription	Brain Inferior Temporal Lobe	brain
4	chr3:50715800-50724600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
5	chr3:50717400-50724600	Weak transcription	HUES6 Cell Line	embryonic stem cell
6	chr3:50717400-50724600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
7	chr3:50721400-50724800	Weak transcription	HSMM	muscle
8	chr3:50722200-50724600	Weak transcription	Brain Anterior Caudate	brain
9	chr3:50723000-50725000	Weak transcription	Brain Substantia Nigra	brain
10	chr3:50723000-50736800	Weak transcription	Brain Hippocampus Middle	brain
11	chr3:50723200-50724600	Weak transcription	Brain Cingulate Gyrus	brain
12	chr3:50723200-50724800	Weak transcription	Brain Angular Gyrus	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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