Variant report

Variant	rs7301328
Chromosome Location	chr12:14018777-14018778
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 4 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:3)

rs_ID	r²[population]
rs10845847	0.82[JPT][hapmap]
rs10845851	0.82[JPT][hapmap]
rs12582848	1.00[CHB][hapmap];0.81[JPT][hapmap];0.84[ASN][1000 genomes]

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	esv3322702	chr12:14018718-14018992	Weak transcription Strong transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:14005200-14020000	Weak transcription	Pancreas	Pancrea
2	chr12:14013400-14019400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr12:14014800-14020800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
4	chr12:14016000-14022800	Weak transcription	HUES48 Cell Line	embryonic stem cell
5	chr12:14017400-14021200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr12:14017800-14019000	Strong transcription	Cortex derived primary cultured neurospheres	brain
7	chr12:14017800-14020600	Weak transcription	A549	lung
8	chr12:14018200-14019400	Weak transcription	Brain Anterior Caudate	brain
9	chr12:14018600-14019400	Enhancers	Fetal Heart	heart

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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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