Variant report

Variant	rs375787787
Chromosome Location	chr2:168340330-168340331
allele	C/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	nsv491872	chr2:168220323-168737986	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	esv3388045	chr2:168289403-168424317	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
3	nsv834449	chr2:168340043-168511856	Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1 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	chr2:168337000-168340400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr2:168337000-168355400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
3	chr2:168337200-168348200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr2:168338200-168343600	Weak transcription	Cortex derived primary cultured neurospheres	brain
5	chr2:168338200-168348200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr2:168338200-168366000	Weak transcription	H1 Cell Line	embryonic stem cell
7	chr2:168338400-168340400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
8	chr2:168338400-168341000	Weak transcription	HUES64 Cell Line	embryonic stem cell
9	chr2:168338400-168349400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
10	chr2:168338400-168352400	Weak transcription	HUES6 Cell Line	embryonic stem cell
11	chr2:168338800-168340400	Weak transcription	HUES48 Cell Line	embryonic stem cell
12	chr2:168338800-168340600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
13	chr2:168340000-168342200	Enhancers	iPS-15b Cell Line	embryonic stem cell
14	chr2:168340200-168345600	Weak transcription	Breast Myoepithelial Primary Cells	Breast

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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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