Variant report

Variant	rs1969837
Chromosome Location	chr6:4020695-4020696
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:14)
CpG islands
(count:0)
Chromatin interactive
region (count:7)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:14 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	TAF1	chr6:4020421-4020733	K562	blood:	n/a	n/a
2	MYC	chr6:4020304-4022486	K562	blood:	n/a	n/a
3	POLR2A	chr6:4020325-4022372	K562	blood:	n/a	n/a
4	ARID3A	chr6:4020502-4020702	K562	blood:	n/a	n/a
5	POLR2A	chr6:4020353-4022370	K562	blood:	n/a	n/a
6	POLR2A	chr6:4020181-4022367	K562	blood:	n/a	n/a
7	ZNF384	chr6:4019933-4020797	K562	blood:	n/a	n/a
8	POLR2A	chr6:4020060-4020991	K562	blood:	n/a	n/a
9	HEY1	chr6:4020377-4020746	K562	blood:	n/a	n/a
10	POLR2A	chr6:4020342-4022148	K562	blood:	n/a	n/a
11	MXI1	chr6:4020413-4023130	SK-N-SH	brain:	n/a	n/a
12	POLR2A	chr6:4017528-4022907	K562	blood:	n/a	n/a
13	POLR2A	chr6:4020291-4022391	K562	blood:	n/a	n/a
14	POLR2A	chr6:4020246-4020781	K562	blood:	n/a	n/a

No data

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:4016355..4024618-chr6:4131840..4138381,21	K562	blood:
2	chr6:4017302..4025509-chr6:4131840..4138381,19	K562	blood:
3	chr6:4019656..4024130-chr6:4049502..4053557,5	K562	blood:
4	chr6:3064193..3067093-chr6:4018828..4021333,2	K562	blood:
5	chr6:4020118..4022120-chr6:4056131..4059470,3	K562	blood:
6	chr6:2988870..2991161-chr6:4018285..4020823,2	K562	blood:
7	chr6:4020118..4023028-chr6:4056131..4059224,3	K562	blood:

No data

Variant related genes	Relation type
PRPF4B	TF binding region
ENSG00000124588	Chromatin interaction
ENSG00000198721	Chromatin interaction
ENSG00000244041	Chromatin interaction
ENSG00000234817	Chromatin interaction
ENSG00000112739	Chromatin interaction
ENSG00000254821	Chromatin interaction
ENSG00000137275	Chromatin interaction
ENSG00000145975	Chromatin interaction

Extended variants
information (count: 30 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs11754326	0.92[ASN][1000 genomes]
rs11754413	0.90[ASN][1000 genomes]
rs11759303	0.94[ASN][1000 genomes]
rs12174184	0.83[EUR][1000 genomes]
rs1408457	0.83[EUR][1000 genomes]
rs17137442	0.92[ASN][1000 genomes]
rs1969836	0.94[AFR][1000 genomes];0.97[AMR][1000 genomes];0.93[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2147374	0.94[ASN][1000 genomes]
rs28889078	0.90[ASN][1000 genomes]
rs4466281	0.82[EUR][1000 genomes]
rs4959916	0.83[EUR][1000 genomes]
rs62394163	0.93[ASN][1000 genomes]
rs6900476	0.83[EUR][1000 genomes]
rs6906467	0.83[EUR][1000 genomes]
rs6910519	0.83[EUR][1000 genomes]
rs6914180	0.83[EUR][1000 genomes]
rs6914776	0.92[ASN][1000 genomes]
rs6930892	0.83[EUR][1000 genomes]
rs9328215	0.83[EUR][1000 genomes]
rs9392546	0.95[AFR][1000 genomes];0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9392547	0.95[AFR][1000 genomes];0.95[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs9392548	0.95[AFR][1000 genomes];0.95[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs9405217	0.95[AFR][1000 genomes];0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9405693	0.93[AFR][1000 genomes];0.95[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs9405694	0.83[EUR][1000 genomes]
rs942474	0.81[EUR][1000 genomes]
rs9503893	0.82[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv532020	chr6:3417520-4140257	Strong transcription Enhancers ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Active TSS Genic enhancers Flanking Bivalent TSS/Enh Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	67 gene(s)	inside rSNPs	diseases
2	nsv1022968	chr6:3862744-4272502	Enhancers Genic enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	56 gene(s)	inside rSNPs	diseases
3	nsv538106	chr6:3862744-4272502	Strong transcription Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	56 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:127 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:4017400-4023000	Active TSS	K562	blood
2	chr6:4019000-4021200	Weak transcription	Gastric	stomach
3	chr6:4019000-4021200	Weak transcription	Spleen	Spleen
4	chr6:4019200-4021000	Weak transcription	Ovary	ovary
5	chr6:4019200-4021200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr6:4019200-4021200	Weak transcription	Esophagus	oesophagus
7	chr6:4019200-4021200	Weak transcription	Lung	lung
8	chr6:4019200-4021200	Flanking Active TSS	Dnd41	blood
9	chr6:4019400-4020800	Enhancers	Cortex derived primary cultured neurospheres	brain
10	chr6:4019400-4020800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr6:4019400-4020800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
12	chr6:4019400-4020800	Enhancers	Fetal Heart	heart
13	chr6:4019400-4020800	Weak transcription	Right Ventricle	heart
14	chr6:4019400-4021000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
15	chr6:4019400-4021000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr6:4019400-4021000	Enhancers	Primary T cells fromperipheralblood	blood
17	chr6:4019400-4021000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
18	chr6:4019400-4021000	Weak transcription	Left Ventricle	heart
19	chr6:4019400-4021000	Weak transcription	Right Atrium	heart
20	chr6:4019400-4021200	Weak transcription	Aorta	Aorta
21	chr6:4019600-4020800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
22	chr6:4019600-4020800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
23	chr6:4019600-4020800	Weak transcription	Muscle Satellite Cultured Cells	--
24	chr6:4019600-4020800	Weak transcription	Brain Angular Gyrus	brain
25	chr6:4019600-4020800	Weak transcription	Brain Anterior Caudate	brain
26	chr6:4019600-4020800	Weak transcription	Brain Inferior Temporal Lobe	brain
27	chr6:4019600-4020800	Weak transcription	Fetal Brain Male	brain
28	chr6:4019600-4020800	Enhancers	Fetal Muscle Leg	muscle
29	chr6:4019600-4020800	Weak transcription	Stomach Smooth Muscle	stomach
30	chr6:4019600-4020800	Enhancers	Thymus	Thymus
31	chr6:4019600-4020800	Weak transcription	HSMMtube	muscle
32	chr6:4019600-4020800	Weak transcription	Osteobl	bone
33	chr6:4019600-4021000	Enhancers	Primary monocytes fromperipheralblood	blood
34	chr6:4019600-4021000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
35	chr6:4019600-4021000	Enhancers	Primary T helper naive cells from peripheral blood	blood
36	chr6:4019600-4021000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
37	chr6:4019600-4021000	Enhancers	Primary T helper cells fromperipheralblood	blood
38	chr6:4019600-4021000	Weak transcription	Rectal Smooth Muscle	rectum
39	chr6:4019600-4021200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
40	chr6:4019600-4023000	Active TSS	HUES64 Cell Line	embryonic stem cell
41	chr6:4019800-4020800	Weak transcription	H1 Cell Line	embryonic stem cell
42	chr6:4019800-4020800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr6:4019800-4020800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
44	chr6:4019800-4020800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
45	chr6:4019800-4020800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
46	chr6:4019800-4020800	Enhancers	Primary B cells from cord blood	blood
47	chr6:4019800-4020800	Enhancers	Primary hematopoietic stem cells	blood
48	chr6:4019800-4020800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
49	chr6:4019800-4020800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
50	chr6:4019800-4020800	Weak transcription	Adipose Nuclei	Adipose

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