Variant report

Variant	rs6114415
Chromosome Location	chr20:24013201-24013202
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 25 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs16986162	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs3848801	0.85[ASN][1000 genomes]
rs6036614	0.98[EUR][1000 genomes]
rs6036617	0.97[ASN][1000 genomes]
rs6036619	1.00[ASN][1000 genomes]
rs6049337	1.00[ASN][1000 genomes]
rs6049338	1.00[ASN][1000 genomes]
rs6049345	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6049347	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6049348	1.00[ASN][1000 genomes]
rs6049349	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6049350	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6049351	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6114419	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6114422	0.92[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs6114423	0.92[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs6114424	0.80[AMR][1000 genomes];0.94[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs62195285	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7344251	0.96[EUR][1000 genomes];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	nsv491876	chr20:23436633-24031374	Weak transcription Flanking Active TSS Enhancers Active TSS Strong transcription Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
2	nsv833944	chr20:23806288-24021865	Bivalent Enhancer Genic enhancers Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
3	nsv1063474	chr20:23918394-24048069	Enhancers Flanking Active TSS ZNF genes & repeats Weak transcription Bivalent Enhancer Genic enhancers Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	nsv9793	chr20:23939613-24734850	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
5	nsv1056491	chr20:23955040-24105080	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
6	nsv585731	chr20:23989027-24024259	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs6114415	FAM154B	trans	lymphoblastoid	seeQTL

Chromatin state (count:19 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:24008400-24013600	Weak transcription	Fetal Thymus	thymus
2	chr20:24008400-24013800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
3	chr20:24008800-24013400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
4	chr20:24012400-24013400	Enhancers	Primary T killer memory cells from peripheral blood	blood
5	chr20:24012400-24014000	Enhancers	Primary B cells from peripheral blood	blood
6	chr20:24012400-24014600	Enhancers	Primary T cells from cord blood	blood
7	chr20:24012400-24014600	Enhancers	Primary T helper cells PMA-I stimulated	--
8	chr20:24012400-24014600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
9	chr20:24012400-24015600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
10	chr20:24012600-24013600	Enhancers	Primary B cells from cord blood	blood
11	chr20:24012600-24014400	Enhancers	Primary T helper naive cells from peripheral blood	blood
12	chr20:24012600-24014600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
13	chr20:24012600-24014600	Enhancers	Primary T helper cells fromperipheralblood	blood
14	chr20:24012600-24014800	Enhancers	Primary T cells fromperipheralblood	blood
15	chr20:24012800-24013800	Enhancers	Dnd41	blood
16	chr20:24013000-24013800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
17	chr20:24013000-24014000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
18	chr20:24013000-24014000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
19	chr20:24013200-24014000	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood

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