Variant report

Variant	rs853410
Chromosome Location	chr6:4058038-4058039
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1)
CpG islands
(count:0)
Chromatin interactive
region (count:6)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

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

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr6:4055073-4058964	K562	blood:	n/a	n/a

No data

(count:6 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:4040955..4045707-chr6:4056854..4061183,4	K562	blood:
2	chr6:4054760..4058464-chr6:4059155..4063115,3	K562	blood:
3	chr6:4020118..4023028-chr6:4056131..4059224,3	K562	blood:
4	chr6:4040955..4043384-chr6:4055982..4058354,2	K562	blood:
5	chr6:4020118..4022120-chr6:4056131..4059470,3	K562	blood:
6	chr6:4057382..4058933-chr6:4121513..4123123,2	K562	blood:

No data

Variant related genes	Relation type
PRPF4B	TF binding region
ENSG00000185689	Chromatin interaction
ENSG00000230648	Chromatin interaction
ENSG00000112739	Chromatin interaction

Extended variants
information (count: 60 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:54)

rs_ID	r²[population]
rs12174184	0.83[ASN][1000 genomes]
rs1408457	0.83[ASN][1000 genomes]
rs1543355	0.81[ASN][1000 genomes]
rs2181894	0.88[ASN][1000 genomes]
rs3747761	0.89[ASN][1000 genomes]
rs3747762	0.89[ASN][1000 genomes]
rs3747763	0.89[ASN][1000 genomes]
rs3761787	0.85[ASN][1000 genomes]
rs4466281	0.83[ASN][1000 genomes]
rs4959916	0.83[ASN][1000 genomes]
rs4959918	0.84[ASN][1000 genomes]
rs4959919	0.80[ASN][1000 genomes]
rs6900476	0.83[ASN][1000 genomes]
rs6905475	0.89[ASN][1000 genomes]
rs6906467	0.83[ASN][1000 genomes]
rs6910519	0.83[ASN][1000 genomes]
rs6914180	0.83[ASN][1000 genomes]
rs6916982	0.86[AMR][1000 genomes];0.81[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6930892	0.83[ASN][1000 genomes]
rs6933593	0.83[ASN][1000 genomes]
rs6941706	0.85[ASN][1000 genomes]
rs697745	0.85[ASN][1000 genomes]
rs707980	0.85[ASN][1000 genomes]
rs707981	0.85[ASN][1000 genomes]
rs707982	0.85[ASN][1000 genomes]
rs707983	0.85[ASN][1000 genomes]
rs707984	0.85[ASN][1000 genomes]
rs707985	0.85[ASN][1000 genomes]
rs707987	0.90[ASN][1000 genomes]
rs707988	0.90[ASN][1000 genomes]
rs7744603	0.83[ASN][1000 genomes]
rs7763233	0.83[ASN][1000 genomes]
rs853396	0.85[ASN][1000 genomes]
rs853397	0.90[ASN][1000 genomes]
rs853398	0.89[ASN][1000 genomes]
rs853399	0.89[ASN][1000 genomes]
rs853400	0.89[ASN][1000 genomes]
rs853402	0.89[ASN][1000 genomes]
rs853403	0.90[ASN][1000 genomes]
rs853404	0.90[ASN][1000 genomes]
rs853405	0.90[ASN][1000 genomes]
rs853406	0.90[ASN][1000 genomes]
rs853407	0.90[ASN][1000 genomes]
rs853408	0.90[ASN][1000 genomes]
rs853409	0.87[ASN][1000 genomes]
rs853411	0.85[ASN][1000 genomes]
rs860477	0.90[ASN][1000 genomes]
rs860478	0.89[ASN][1000 genomes]
rs9328215	0.83[ASN][1000 genomes]
rs9328216	0.87[ASN][1000 genomes]
rs9405694	0.83[ASN][1000 genomes]
rs941443	0.81[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs942474	0.83[ASN][1000 genomes]
rs9503893	0.83[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	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
4	nsv1034223	chr6:4030708-4060347	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
5	nsv462615	chr6:4052383-4096678	Strong transcription Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
6	nsv600860	chr6:4052383-4096678	Strong transcription Weak transcription Enhancers Bivalent Enhancer Genic enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:126 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:4023000-4063600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr6:4023200-4064000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr6:4023400-4071600	Weak transcription	Stomach Mucosa	stomach
4	chr6:4023800-4067000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr6:4024600-4059200	Strong transcription	Fetal Thymus	thymus
6	chr6:4027200-4058200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
7	chr6:4030600-4065800	Strong transcription	iPS-18 Cell Line	embryonic stem cell
8	chr6:4030800-4059000	Strong transcription	HUES64 Cell Line	embryonic stem cell
9	chr6:4030800-4066600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr6:4031000-4059200	Strong transcription	HUES6 Cell Line	embryonic stem cell
11	chr6:4031000-4066400	Strong transcription	HUES48 Cell Line	embryonic stem cell
12	chr6:4031200-4066600	Strong transcription	Monocytes-CD14+_RO01746	blood
13	chr6:4034000-4066800	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr6:4035600-4063600	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
15	chr6:4035600-4064200	Strong transcription	H1 Cell Line	embryonic stem cell
16	chr6:4035800-4058400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr6:4035800-4058600	Strong transcription	Primary T cells from cord blood	blood
18	chr6:4035800-4064600	Strong transcription	Primary B cells from peripheral blood	blood
19	chr6:4035800-4065000	Strong transcription	Dnd41	blood
20	chr6:4035800-4066000	Strong transcription	Primary monocytes fromperipheralblood	blood
21	chr6:4035800-4066000	Strong transcription	Rectal Mucosa Donor 29	rectum
22	chr6:4035800-4066200	Strong transcription	iPS-20b Cell Line	embryonic stem cell
23	chr6:4036000-4058200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
24	chr6:4036000-4066600	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
25	chr6:4036000-4066600	Strong transcription	Duodenum Mucosa	Duodenum
26	chr6:4037200-4059400	Strong transcription	Primary T cells fromperipheralblood	blood
27	chr6:4037200-4066200	Strong transcription	Liver	Liver
28	chr6:4037400-4058400	Strong transcription	HepG2	liver
29	chr6:4037400-4059400	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
30	chr6:4037400-4065800	Strong transcription	Placenta	Placenta
31	chr6:4037600-4066200	Strong transcription	Rectal Mucosa Donor 31	rectum
32	chr6:4037600-4066400	Strong transcription	Primary neutrophils fromperipheralblood	blood
33	chr6:4037800-4058600	Strong transcription	Primary T helper cells fromperipheralblood	blood
34	chr6:4037800-4058600	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
35	chr6:4037800-4058800	Strong transcription	Primary T helper naive cells from peripheral blood	blood
36	chr6:4037800-4059400	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
37	chr6:4038200-4058200	Strong transcription	Primary T helper cells PMA-I stimulated	--
38	chr6:4038800-4058200	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
39	chr6:4038800-4066000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
40	chr6:4040000-4058600	Strong transcription	Colon Smooth Muscle	Colon
41	chr6:4040200-4058200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
42	chr6:4040800-4065400	Strong transcription	GM12878-XiMat	blood
43	chr6:4042000-4066400	Strong transcription	Adipose Nuclei	Adipose
44	chr6:4047400-4059200	Strong transcription	Primary T killer memory cells from peripheral blood	blood
45	chr6:4047600-4058200	Strong transcription	Primary T killer naive cells fromperipheralblood	blood
46	chr6:4047800-4058400	Strong transcription	Primary hematopoietic stem cells	blood
47	chr6:4048200-4063600	Strong transcription	Left Ventricle	heart
48	chr6:4048200-4063600	Strong transcription	Thymus	Thymus
49	chr6:4048200-4064000	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
50	chr6:4048200-4064600	Strong transcription	Fetal Intestine Large	intestine

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