Variant report

Variant	rs540070017
Chromosome Location	chr14:78828660-78828661
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 9 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv832837	chr14:78766805-78946526	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
2	esv2440961	chr14:78827652-78829318	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	n/a
3	esv5980	chr14:78827960-78828843	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	n/a
4	esv2080567	chr14:78828056-78828791	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	n/a
5	esv3530257	chr14:78828125-78828669	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	n/a
6	esv3508042	chr14:78828133-78828688	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	n/a
7	esv3508036	chr14:78828148-78828680	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	n/a
8	esv3189	chr14:78828160-78828683	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	n/a
9	esv989776	chr14:78828200-78828989	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	n/a

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:78826400-78833200	Weak transcription	Brain Germinal Matrix	brain
2	chr14:78827000-78833400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
3	chr14:78827400-78833200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr14:78827800-78831800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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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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