Variant report

Variant	rs2220192
Chromosome Location	chr14:97379289-97379290
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 18 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs1385553	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1385554	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2062386	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs4900355	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs4905565	1.00[AFR][1000 genomes]
rs4905569	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6575602	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs710264	1.00[AMR][1000 genomes]
rs8022166	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs856224	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs856258	1.00[AMR][1000 genomes]
rs856260	1.00[AMR][1000 genomes]
rs856272	1.00[AMR][1000 genomes]
rs9323956	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1044202	chr14:97155291-97683983	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
2	nsv542179	chr14:97155291-97683983	Weak transcription Strong transcription Bivalent/Poised TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
3	nsv948620	chr14:97334444-98133191	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
4	nsv832867	chr14:97365919-97541763	Bivalent/Poised TSS Enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Weak transcription Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 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	chr14:97368600-97391400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr14:97376800-97387600	Weak transcription	Thymus	Thymus
3	chr14:97377200-97380400	Weak transcription	Fetal Muscle Trunk	muscle
4	chr14:97377400-97379400	Enhancers	Primary T cells from cord blood	blood
5	chr14:97377600-97379800	Enhancers	Primary T cells fromperipheralblood	blood
6	chr14:97377600-97380600	Weak transcription	Dnd41	blood
7	chr14:97378400-97383000	Weak transcription	K562	blood
8	chr14:97379000-97379400	Weak transcription	Fetal Muscle Leg	muscle
9	chr14:97379000-97380600	Weak transcription	Spleen	Spleen
10	chr14:97379000-97387800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin

Quick Search:

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

what's new

Quick links