Variant report

Variant	rs1540332
Chromosome Location	chr7:25618842-25618843
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 21 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:18)

rs_ID	r²[population]
rs1074503	0.82[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs1074504	0.82[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs10951079	0.92[AFR][1000 genomes];0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11971048	0.82[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs11981833	0.82[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs11981887	0.82[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs11982106	0.82[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs12216588	0.94[AFR][1000 genomes];0.85[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs1502949	0.82[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs1502950	0.82[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs17367291	0.82[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs17464658	0.92[ASN][1000 genomes]
rs1995437	0.80[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs2074137	0.89[AFR][1000 genomes];0.88[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs3887045	0.82[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73693187	0.82[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs739624	0.96[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs882101	1.00[ASN][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	nsv606426	chr7:25254125-25621579	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
2	nsv1016813	chr7:25405859-26150509	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	108 gene(s)	inside rSNPs	diseases
3	nsv538803	chr7:25405859-26150509	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	108 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:25617200-25621400	Enhancers	Rectal Mucosa Donor 31	rectum
2	chr7:25617600-25619200	Enhancers	Fetal Lung	lung
3	chr7:25617600-25621400	Enhancers	Fetal Intestine Large	intestine
4	chr7:25618600-25619000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
5	chr7:25618800-25619400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
6	chr7:25618800-25619600	Enhancers	Fetal Stomach	stomach
7	chr7:25618800-25619600	Enhancers	K562	blood
8	chr7:25618800-25620600	Enhancers	Duodenum Mucosa	Duodenum
9	chr7:25618800-25620800	Enhancers	Rectal Mucosa Donor 29	rectum
10	chr7:25618800-25621000	Enhancers	Fetal Intestine Small	intestine

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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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