Variant report

Variant	rs34721518
Chromosome Location	chr8:130016968-130016969
allele	-/A
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	nsv437633	chr8:130014200-130022257	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	n/a	inside rSNPs	n/a
2	nsv891442	chr8:130016499-130130604	Enhancers Transcr. at gene 5' and 3' Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	nsv891443	chr8:130016499-130220746	Weak transcription Flanking Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats Active TSS	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:130011800-130017200	Weak transcription	Osteobl	bone
2	chr8:130012000-130017000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
3	chr8:130012000-130017200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr8:130012200-130017200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
5	chr8:130014600-130017000	Weak transcription	Muscle Satellite Cultured Cells	--
6	chr8:130014600-130017200	Weak transcription	Fetal Stomach	stomach
7	chr8:130015000-130017000	Weak transcription	HSMMtube	muscle
8	chr8:130015400-130017000	Weak transcription	HSMM	muscle
9	chr8:130015400-130017200	Weak transcription	Dnd41	blood
10	chr8:130016000-130017200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
11	chr8:130016000-130017200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
12	chr8:130016400-130017400	Weak transcription	Fetal Muscle Leg	muscle
13	chr8:130016600-130018400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	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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