Variant report

Variant	rs1512325
Chromosome Location	chr4:149289693-149289694
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:14)

rs_ID	r²[population]
rs11724226	0.87[AMR][1000 genomes];0.86[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs12711260	0.87[AMR][1000 genomes];0.85[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs13109808	0.95[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs13109933	0.84[ASN][1000 genomes]
rs13112423	0.81[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs13127625	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs13137655	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs13144019	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1512327	0.87[AMR][1000 genomes];0.86[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1512341	0.88[AMR][1000 genomes];0.85[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2137331	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6831212	0.88[AMR][1000 genomes];0.87[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7696770	0.92[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs992556	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];0.86[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1027263	chr4:149127120-149320135	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv537296	chr4:149127120-149320135	Flanking Active TSS Weak transcription Enhancers Active TSS ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	nsv1016966	chr4:149209467-149341037	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	esv3584816	chr4:149254670-149293317	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
5	nsv530433	chr4:149277637-149669181	Weak transcription Enhancers Flanking Bivalent TSS/Enh Active TSS Genic enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
6	nsv880246	chr4:149287807-149311728	Flanking Active TSS Enhancers Active TSS Weak transcription ZNF genes & repeats	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:18 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:149277000-149291000	Weak transcription	Left Ventricle	heart
2	chr4:149277000-149296800	Weak transcription	Rectal Mucosa Donor 31	rectum
3	chr4:149277000-149306800	Weak transcription	Pancreas	Pancrea
4	chr4:149281200-149300800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
5	chr4:149281400-149290800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
6	chr4:149282800-149296800	Weak transcription	Psoas Muscle	Psoas
7	chr4:149283000-149299000	Weak transcription	Sigmoid Colon	Sigmoid Colon
8	chr4:149283200-149293400	Weak transcription	Right Atrium	heart
9	chr4:149288400-149291000	Weak transcription	Skeletal Muscle Male	skeletal muscle
10	chr4:149288400-149297000	Weak transcription	Fetal Heart	heart
11	chr4:149289400-149290000	Weak transcription	Aorta	Aorta
12	chr4:149289400-149291200	Weak transcription	Spleen	Spleen
13	chr4:149289400-149293400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
14	chr4:149289400-149294200	Weak transcription	Primary T helper cells PMA-I stimulated	--
15	chr4:149289400-149294200	Weak transcription	Primary T helper cells fromperipheralblood	blood
16	chr4:149289600-149291000	Weak transcription	Skeletal Muscle Female	skeletal muscle
17	chr4:149289600-149294200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
18	chr4:149289600-149297000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood

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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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