Variant report

Variant	rs7606215
Chromosome Location	chr2:169766938-169766939
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 14 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs10497346	0.92[EUR][1000 genomes]
rs12475693	0.84[AFR][1000 genomes]
rs16856159	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs16856161	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs1879696	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2232316	0.88[AFR][1000 genomes];0.82[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs2232328	0.97[EUR][1000 genomes]
rs3770568	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs3821117	0.86[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs56135702	0.93[EUR][1000 genomes]
rs6730651	0.92[EUR][1000 genomes]

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	nsv583599	chr2:169664227-169903096	Bivalent Enhancer Weak transcription Genic enhancers Strong transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
2	nsv459943	chr2:169756930-169799010	Bivalent/Poised TSS Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region miRNA target site	4 gene(s)	inside rSNPs	diseases
3	nsv583600	chr2:169756930-169799010	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region miRNA target site	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:19 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:169764400-169768400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr2:169764400-169768400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr2:169764600-169768400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr2:169764600-169768600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
5	chr2:169764800-169768200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
6	chr2:169766200-169768400	Enhancers	iPS-15b Cell Line	embryonic stem cell
7	chr2:169766400-169767200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
8	chr2:169766400-169767200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
9	chr2:169766400-169768400	Enhancers	HUES6 Cell Line	embryonic stem cell
10	chr2:169766600-169767200	Enhancers	H9 Cell Line	embryonic stem cell
11	chr2:169766600-169767400	Enhancers	iPS-18 Cell Line	embryonic stem cell
12	chr2:169766600-169767600	Enhancers	HUES64 Cell Line	embryonic stem cell
13	chr2:169766600-169768800	Enhancers	HUES48 Cell Line	embryonic stem cell
14	chr2:169766800-169767000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
15	chr2:169766800-169767000	Enhancers	Fetal Brain Female	brain
16	chr2:169766800-169767200	Enhancers	H1 Cell Line	embryonic stem cell
17	chr2:169766800-169767200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
18	chr2:169766800-169767400	Enhancers	iPS-20b Cell Line	embryonic stem cell
19	chr2:169766800-169768200	Weak transcription	Pancreatic Islets	Pancreatic Islet

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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