Variant report

Variant	rs564775800
Chromosome Location	chr12:106671157-106671158
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 6 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:6 , 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
3	esv3492374	chr12:106670673-106671418	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
4	esv3429578	chr12:106670686-106671452	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
5	esv3327586	chr12:106670744-106671378	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
6	esv3492408	chr12:106670758-106671379	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:14 , 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	chr12:106669600-106671200	Weak transcription	Rectal Mucosa Donor 31	rectum
3	chr12:106669600-106671800	Weak transcription	Rectal Mucosa Donor 29	rectum
4	chr12:106669600-106672800	Weak transcription	Liver	Liver
5	chr12:106669600-106673800	Weak transcription	Pancreatic Islets	Pancreatic Islet
6	chr12:106670200-106671200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
7	chr12:106670200-106671400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr12:106670200-106671400	Weak transcription	Sigmoid Colon	Sigmoid Colon
9	chr12:106670400-106673000	Weak transcription	Monocytes-CD14+_RO01746	blood
10	chr12:106670400-106673200	Weak transcription	Primary monocytes fromperipheralblood	blood
11	chr12:106670800-106671200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
12	chr12:106670800-106671400	Enhancers	Stomach Mucosa	stomach
13	chr12:106670800-106671800	Enhancers	Fetal Heart	heart
14	chr12:106670800-106672800	Enhancers	Primary neutrophils fromperipheralblood	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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