Variant report

Variant	rs61762842
Chromosome Location	chr4:149289018-149289019
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 14 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:8)

rs_ID	r²[population]
rs10018805	1.00[ASN][1000 genomes]
rs10519945	1.00[ASN][1000 genomes]
rs12511893	1.00[ASN][1000 genomes]
rs3846303	1.00[ASN][1000 genomes]
rs61758358	1.00[ASN][1000 genomes]
rs61760326	1.00[ASN][1000 genomes]
rs61762856	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6848375	1.00[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:17 , 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	chr4:149282800-149289200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
7	chr4:149282800-149296800	Weak transcription	Psoas Muscle	Psoas
8	chr4:149283000-149299000	Weak transcription	Sigmoid Colon	Sigmoid Colon
9	chr4:149283200-149293400	Weak transcription	Right Atrium	heart
10	chr4:149287800-149289600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
11	chr4:149288400-149291000	Weak transcription	Skeletal Muscle Male	skeletal muscle
12	chr4:149288400-149297000	Weak transcription	Fetal Heart	heart
13	chr4:149288800-149289400	Enhancers	Primary T helper cells fromperipheralblood	blood
14	chr4:149289000-149289400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
15	chr4:149289000-149289400	Enhancers	Primary T helper cells PMA-I stimulated	--
16	chr4:149289000-149289400	Enhancers	Gastric	stomach
17	chr4:149289000-149289600	Enhancers	Skeletal Muscle Female	skeletal muscle

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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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