Variant report

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs11840421	0.83[ASW][hapmap];1.00[CEU][hapmap];1.00[TSI][hapmap];1.00[EUR][1000 genomes]
rs11840494	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11841861	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs11841891	0.83[ASW][hapmap];1.00[CEU][hapmap];1.00[TSI][hapmap];1.00[EUR][1000 genomes]
rs11843185	0.99[ASN][1000 genomes]
rs17058278	1.00[ASN][1000 genomes]
rs17058280	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17058283	1.00[ASN][1000 genomes]
rs17058288	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17058294	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55731466	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55999507	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56002018	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs57803668	1.00[ASN][1000 genomes]
rs58251872	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59102087	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73450054	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs74050066	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs74050067	1.00[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs74050068	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][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	nsv832584	chr13:39074265-39284724	Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Active TSS Strong transcription ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:15 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:39172800-39187600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr13:39181400-39186000	Weak transcription	HUES6 Cell Line	embryonic stem cell
3	chr13:39181800-39186000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
4	chr13:39181800-39187200	Weak transcription	H1 Cell Line	embryonic stem cell
5	chr13:39182200-39186000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
6	chr13:39182400-39186200	Weak transcription	HUES48 Cell Line	embryonic stem cell
7	chr13:39182600-39187200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
8	chr13:39184400-39186600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
9	chr13:39185600-39186000	Enhancers	Fetal Intestine Small	intestine
10	chr13:39185600-39186400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr13:39185600-39186400	Enhancers	Fetal Kidney	kidney
12	chr13:39185600-39186600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
13	chr13:39185800-39186000	Enhancers	Duodenum Mucosa	Duodenum
14	chr13:39185800-39186000	Enhancers	Hela-S3	cervix
15	chr13:39185800-39186400	Enhancers	H9 Cell Line	embryonic stem cell

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