Variant report

Variant	rs8100861
Chromosome Location	chr19:51895119-51895120
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr19:51894435..51896093-chr19:51896097..51897636,2	K562	blood:
2	chr19:51895053..51897765-chr19:52007493..52009642,2	K562	blood:
3	chr19:51894612..51896721-chr19:52196678..52199647,2	K562	blood:
4	chr19:51840838..51845657-chr19:51892354..51900411,18	K562	blood:
5	chr19:51867772..51875803-chr19:51892381..51899756,21	K562	blood:
6	chr19:51864453..51872845-chr19:51892428..51902096,29	K562	blood:
7	chr19:51889722..51893942-chr19:51894149..51900029,8	K562	blood:

Variant related genes	Relation type
ENSG00000269959	Chromatin interaction
ENSG00000268520	Chromatin interaction
ENSG00000105374	Chromatin interaction
ENSG00000186806	Chromatin interaction
ENSG00000105370	Chromatin interaction
ENSG00000268839	Chromatin interaction
ENSG00000267905	Chromatin interaction
ENSG00000262874	Chromatin interaction
ENSG00000105379	Chromatin interaction
ENSG00000182310	Chromatin interaction
ENSG00000160318	Chromatin interaction
ENSG00000269403	Chromatin interaction

Extended variants
information (count: 41 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:39)

rs_ID	r²[population]
rs10403762	0.90[ASN][1000 genomes]
rs10404198	0.98[AFR][1000 genomes];0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10419880	0.92[ASN][1000 genomes]
rs11084075	0.84[AMR][1000 genomes];0.85[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11084076	0.84[AMR][1000 genomes];0.85[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11084077	0.94[ASN][1000 genomes]
rs11669975	0.96[AFR][1000 genomes];0.97[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11670065	0.98[AFR][1000 genomes];0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11673263	0.92[AFR][1000 genomes];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2411321	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2411322	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2547308	0.88[ASN][1000 genomes]
rs2547309	0.88[ASN][1000 genomes]
rs2741240	0.84[ASN][1000 genomes]
rs2741241	0.90[ASN][1000 genomes]
rs3810093	0.89[ASN][1000 genomes]
rs3810094	0.90[ASN][1000 genomes]
rs3810095	0.89[ASN][1000 genomes]
rs3810096	0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs3810097	0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs3826657	0.89[ASN][1000 genomes]
rs3826658	0.89[ASN][1000 genomes]
rs3826659	0.88[ASN][1000 genomes]
rs3826660	0.89[ASN][1000 genomes]
rs3826663	0.89[ASN][1000 genomes]
rs3826664	0.89[ASN][1000 genomes]
rs3826665	0.89[ASN][1000 genomes]
rs4377257	0.84[AMR][1000 genomes];0.85[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4441376	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7250926	0.98[AFR][1000 genomes];0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7251238	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7251286	0.88[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs7251311	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7251566	0.98[AFR][1000 genomes];0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7257275	0.84[AMR][1000 genomes];0.85[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7508570	0.82[AMR][1000 genomes];0.85[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs8104425	0.89[ASN][1000 genomes]
rs8107533	0.85[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs8111906	0.84[AMR][1000 genomes];0.85[EUR][1000 genomes];0.92[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1066308	chr19:51680133-52103974	Active TSS Weak transcription Flanking Active TSS Enhancers Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	71 gene(s)	inside rSNPs	diseases
2	nsv544049	chr19:51680133-52103974	Bivalent Enhancer Strong transcription Enhancers Active TSS Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	71 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs8100861	CTD-2616J11.4	cis	Whole Blood	GTEx

Chromatin state (count:60 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:51872000-51897000	Weak transcription	Right Atrium	heart
2	chr19:51889200-51897000	Weak transcription	Spleen	Spleen
3	chr19:51891000-51897000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
4	chr19:51891600-51897000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
5	chr19:51891800-51897000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr19:51891800-51897000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr19:51891800-51897000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr19:51892600-51897000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
9	chr19:51894200-51896800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr19:51894200-51897000	Weak transcription	H1 Cell Line	embryonic stem cell
11	chr19:51894200-51897000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
12	chr19:51894200-51897000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
13	chr19:51894200-51897000	Weak transcription	Placenta	Placenta
14	chr19:51894200-51897000	Weak transcription	Fetal Stomach	stomach
15	chr19:51894400-51896800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
16	chr19:51894400-51897000	Weak transcription	HUES64 Cell Line	embryonic stem cell
17	chr19:51894400-51897000	Weak transcription	Primary T cells from cord blood	blood
18	chr19:51894400-51897000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
19	chr19:51894400-51897000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
20	chr19:51894400-51897000	Weak transcription	Fetal Muscle Leg	muscle
21	chr19:51894400-51897000	Weak transcription	Rectal Smooth Muscle	rectum
22	chr19:51894400-51897000	Weak transcription	NHDF-Ad	bronchial
23	chr19:51894400-51897000	Weak transcription	Osteobl	bone
24	chr19:51894400-51897200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
25	chr19:51894600-51896000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
26	chr19:51894600-51896200	Weak transcription	Primary T helper cells PMA-I stimulated	--
27	chr19:51894600-51896800	Weak transcription	HUES6 Cell Line	embryonic stem cell
28	chr19:51894600-51896800	Weak transcription	Sigmoid Colon	Sigmoid Colon
29	chr19:51894600-51897000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
30	chr19:51894600-51897000	Weak transcription	HUES48 Cell Line	embryonic stem cell
31	chr19:51894600-51897000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
32	chr19:51894600-51897000	Weak transcription	Primary neutrophils fromperipheralblood	blood
33	chr19:51894600-51897000	Weak transcription	Primary B cells from cord blood	blood
34	chr19:51894600-51897000	Weak transcription	Primary B cells from peripheral blood	blood
35	chr19:51894600-51897000	Weak transcription	Primary hematopoietic stem cells	blood
36	chr19:51894600-51897000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
37	chr19:51894600-51897000	Weak transcription	Esophagus	oesophagus
38	chr19:51894600-51897000	Weak transcription	Fetal Lung	lung
39	chr19:51894600-51897000	Weak transcription	Fetal Muscle Trunk	muscle
40	chr19:51894600-51897000	Weak transcription	Thymus	Thymus
41	chr19:51894800-51896000	Weak transcription	GM12878-XiMat	blood
42	chr19:51894800-51896800	Weak transcription	Primary T cells fromperipheralblood	blood
43	chr19:51894800-51897000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
44	chr19:51894800-51897000	Weak transcription	H9 Cell Line	embryonic stem cell
45	chr19:51894800-51897000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
46	chr19:51894800-51897000	Weak transcription	Primary monocytes fromperipheralblood	blood
47	chr19:51894800-51897000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
48	chr19:51894800-51897000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
49	chr19:51894800-51897000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
50	chr19:51894800-51897000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood

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