Variant report

Variant	rs4972598
Chromosome Location	chr2:172973949-172973950
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 2 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv518335	chr2:172972971-172974749	Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	esv3436324	chr2:172973656-172974704	Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:172968000-172974800	Weak transcription	Gastric	stomach
2	chr2:172971600-172975200	Bivalent Enhancer	Fetal Thymus	thymus
3	chr2:172971800-172974200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
4	chr2:172971800-172974200	Weak transcription	NHEK	skin
5	chr2:172971800-172974400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
6	chr2:172971800-172974600	Weak transcription	HMEC	breast
7	chr2:172972600-172974200	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr2:172972600-172974400	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
9	chr2:172972600-172974800	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
10	chr2:172973000-172978200	Weak transcription	NHDF-Ad	bronchial
11	chr2:172973200-172974000	Bivalent Enhancer	Primary T cells from cord blood	blood
12	chr2:172973200-172974400	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
13	chr2:172973200-172974600	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
14	chr2:172973400-172974000	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
15	chr2:172973400-172974800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
16	chr2:172973600-172974400	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
17	chr2:172973600-172974800	Bivalent Enhancer	HepG2	liver
18	chr2:172973800-172975000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin

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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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