Variant report

Variant	rs13087943
Chromosome Location	chr3:142413600-142413601
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 20 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:17)

rs_ID	r²[population]
rs10935467	0.86[AFR][1000 genomes]
rs11915810	0.86[AFR][1000 genomes]
rs11929069	0.82[YRI][hapmap];0.91[AFR][1000 genomes];0.93[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs13060062	0.96[EUR][1000 genomes]
rs13064897	0.82[AFR][1000 genomes];0.85[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs13081255	0.81[AFR][1000 genomes]
rs13092601	0.95[AFR][1000 genomes];0.87[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs1916638	0.82[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs34084493	0.86[AFR][1000 genomes]
rs34485065	0.93[AFR][1000 genomes];0.92[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs34941168	0.82[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs36085850	0.86[AFR][1000 genomes]
rs55968753	0.95[AFR][1000 genomes];0.93[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs62278490	0.84[AFR][1000 genomes];0.87[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs62278492	0.89[AFR][1000 genomes];0.87[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs62278493	0.84[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs62278494	0.86[AFR][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	nsv932989	chr3:142204208-142423305	Weak transcription Strong transcription Active TSS Flanking Active TSS Enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases
2	nsv591920	chr3:142411200-142496951	Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription Strong transcription Active TSS Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region miRNA target site	8 gene(s)	inside rSNPs	diseases
3	nsv521098	chr3:142411200-142503605	Weak transcription Active TSS Enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region miRNA target site	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:17 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:142366000-142435400	Weak transcription	Colonic Mucosa	Colon
2	chr3:142385800-142415400	Weak transcription	A549	lung
3	chr3:142389200-142414800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
4	chr3:142389800-142442400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
5	chr3:142392800-142418000	Weak transcription	HepG2	liver
6	chr3:142392800-142425400	Weak transcription	Dnd41	blood
7	chr3:142392800-142433000	Weak transcription	Sigmoid Colon	Sigmoid Colon
8	chr3:142393000-142426000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr3:142393400-142426200	Weak transcription	Primary hematopoietic stem cells	blood
10	chr3:142404200-142418000	Weak transcription	HMEC	breast
11	chr3:142404600-142416200	Weak transcription	Fetal Intestine Small	intestine
12	chr3:142407200-142417000	Weak transcription	HUES48 Cell Line	embryonic stem cell
13	chr3:142408800-142430400	Weak transcription	Liver	Liver
14	chr3:142411800-142413600	Enhancers	NHEK	skin
15	chr3:142412800-142416600	Weak transcription	Rectal Mucosa Donor 31	rectum
16	chr3:142412800-142426600	Weak transcription	Rectal Mucosa Donor 29	rectum
17	chr3:142413200-142422600	Weak transcription	Duodenum Mucosa	Duodenum

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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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