Variant report

Variant	rs13211381
Chromosome Location	chr6:150693657-150693658
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 3 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2763602	chr6:150581193-150720666	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
2	esv3370261	chr6:150692709-150694807	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	n/a	inside rSNPs	n/a
3	esv1594235	chr6:150693563-150693689	Enhancers Weak transcription	n/a	n/a	inside rSNPs	n/a

No data

Chromatin state (count:18 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:150691000-150698200	Weak transcription	Stomach Mucosa	stomach
2	chr6:150691600-150700200	Weak transcription	Lung	lung
3	chr6:150691800-150695000	Enhancers	Liver	Liver
4	chr6:150692200-150694600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr6:150692200-150698200	Weak transcription	Duodenum Mucosa	Duodenum
6	chr6:150692400-150695200	Enhancers	Muscle Satellite Cultured Cells	--
7	chr6:150692600-150694000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
8	chr6:150692800-150695000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
9	chr6:150692800-150695400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr6:150692800-150695600	Enhancers	Osteobl	bone
11	chr6:150693000-150695400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
12	chr6:150693000-150695400	Enhancers	NHDF-Ad	bronchial
13	chr6:150693200-150694000	Enhancers	Right Atrium	heart
14	chr6:150693200-150698400	Weak transcription	Fetal Intestine Large	intestine
15	chr6:150693400-150693800	Weak transcription	NH-A	brain
16	chr6:150693400-150698000	Weak transcription	Fetal Intestine Small	intestine
17	chr6:150693400-150698400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
18	chr6:150693600-150694000	Enhancers	Left Ventricle	heart

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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