Variant report

Variant	rs188019603
Chromosome Location	chr12:106671459-106671460
allele	C/T
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	esv3492397	chr12:106670621-106671491	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
2	esv3492385	chr12:106670666-106671470	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:106666200-106680800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
2	chr12:106669600-106671800	Weak transcription	Rectal Mucosa Donor 29	rectum
3	chr12:106669600-106672800	Weak transcription	Liver	Liver
4	chr12:106669600-106673800	Weak transcription	Pancreatic Islets	Pancreatic Islet
5	chr12:106670400-106673000	Weak transcription	Monocytes-CD14+_RO01746	blood
6	chr12:106670400-106673200	Weak transcription	Primary monocytes fromperipheralblood	blood
7	chr12:106670800-106671800	Enhancers	Fetal Heart	heart
8	chr12:106670800-106672800	Enhancers	Primary neutrophils fromperipheralblood	blood
9	chr12:106671200-106673200	Enhancers	Rectal Mucosa Donor 31	rectum
10	chr12:106671400-106672000	Enhancers	Sigmoid Colon	Sigmoid Colon
11	chr12:106671400-106674800	Weak transcription	Stomach Mucosa	stomach

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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