Variant report

Variant	rs2996687
Chromosome Location	chr1:209373966-209373967
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 23 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:22)

rs_ID	r²[population]
rs1933612	0.84[JPT][hapmap]
rs1933619	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs2250701	1.00[JPT][hapmap]
rs2266024	0.81[EUR][1000 genomes]
rs2788158	0.89[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2788159	0.88[AMR][1000 genomes];0.90[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2788161	0.81[EUR][1000 genomes]
rs2788162	0.91[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs2788168	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs2788170	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs2970555	0.95[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs2970556	0.83[AFR][1000 genomes];0.97[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs2970560	0.98[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs2996683	0.97[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs2996688	0.97[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs34523921	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs34944110	0.88[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs4396124	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs6658956	0.85[JPT][hapmap]
rs6672407	0.85[JPT][hapmap]
rs6704132	0.82[JPT][hapmap]
rs71636106	0.91[AMR][1000 genomes];0.96[EUR][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	nsv832481	chr1:209371276-209540333	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:20 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:209370400-209380800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr1:209372000-209374200	Enhancers	H9 Cell Line	embryonic stem cell
3	chr1:209373200-209374000	Enhancers	HUES6 Cell Line	embryonic stem cell
4	chr1:209373200-209374200	Enhancers	iPS-18 Cell Line	embryonic stem cell
5	chr1:209373200-209380800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
6	chr1:209373200-209381200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
7	chr1:209373400-209376200	Weak transcription	Fetal Brain Female	brain
8	chr1:209373600-209374000	Enhancers	HUES64 Cell Line	embryonic stem cell
9	chr1:209373600-209374000	Enhancers	iPS-15b Cell Line	embryonic stem cell
10	chr1:209373600-209376200	Weak transcription	Fetal Brain Male	brain
11	chr1:209373600-209376600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
12	chr1:209373600-209376600	Weak transcription	Brain Germinal Matrix	brain
13	chr1:209373600-209380400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr1:209373800-209374000	Enhancers	iPS-20b Cell Line	embryonic stem cell
15	chr1:209373800-209374800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
16	chr1:209373800-209375000	Weak transcription	H1 Cell Line	embryonic stem cell
17	chr1:209373800-209375600	Weak transcription	Cortex derived primary cultured neurospheres	brain
18	chr1:209373800-209376400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
19	chr1:209373800-209376600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
20	chr1:209373800-209376600	Weak transcription	HUES48 Cell Line	embryonic stem cell

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