Variant report

Variant	rs9461414
Chromosome Location	chr6:27791063-27791064
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:12)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:26204679..26206586-chr6:27790923..27793517,4	K562	blood:
2	chr6:27098197..27103724-chr6:27790239..27793900,13	K562	blood:
3	chr6:27112528..27118803-chr6:27787647..27794623,16	K562	blood:
4	chr6:26203034..26206484-chr6:27789284..27793104,6	MCF-7	breast:
5	chr6:27103857..27108544-chr6:27789458..27794450,6	K562	blood:
6	chr6:26215488..26220486-chr6:27788576..27794997,7	K562	blood:
7	chr6:26156539..26159752-chr6:27789792..27793850,5	MCF-7	breast:
8	chr6:27093465..27120217-chr6:27768366..27817187,256	K562	blood:
9	chr6:26215362..26217924-chr6:27790762..27793250,4	MCF-7	breast:
10	chr6:26283774..26285764-chr6:27791060..27793861,2	MCF-7	breast:
11	chr6:26030055..26033247-chr6:27790818..27793416,3	MCF-7	breast:
12	chr6:27100619..27103482-chr6:27790924..27794224,3	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000184825	Chromatin interaction
ENSG00000198339	Chromatin interaction
ENSG00000196787	Chromatin interaction
ENSG00000265565	Chromatin interaction
ENSG00000168274	Chromatin interaction
ENSG00000124635	Chromatin interaction
ENSG00000168298	Chromatin interaction
ENSG00000197903	Chromatin interaction
ENSG00000187990	Chromatin interaction
ENSG00000158373	Chromatin interaction
ENSG00000198518	Chromatin interaction
ENSG00000124693	Chromatin interaction
ENSG00000158406	Chromatin interaction

Extended variants
information (count: 12 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:7)

rs_ID	r²[population]
rs10080283	1.00[YRI][hapmap];1.00[AMR][1000 genomes]
rs6911912	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9295748	1.00[YRI][hapmap];1.00[AMR][1000 genomes]
rs9468224	1.00[AMR][1000 genomes]
rs9468233	1.00[YRI][hapmap];1.00[AMR][1000 genomes]
rs9468234	1.00[AMR][1000 genomes]
rs9468244	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1022797	chr6:27396961-27864277	Enhancers Weak transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	390 gene(s)	inside rSNPs	diseases
2	nsv432858	chr6:27719375-28011652	Flanking Active TSS Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	387 gene(s)	inside rSNPs	diseases
3	nsv1017440	chr6:27734824-27864277	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	370 gene(s)	inside rSNPs	diseases
4	nsv1022173	chr6:27734824-27959408	Enhancers Flanking Active TSS Active TSS Weak transcription Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	379 gene(s)	inside rSNPs	diseases
5	nsv883512	chr6:27748631-27969004	Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	379 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:48 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:27783400-27791200	Weak transcription	Liver	Liver
2	chr6:27783400-27791800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr6:27784000-27791200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
4	chr6:27787800-27791200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
5	chr6:27787800-27791200	Weak transcription	Fetal Thymus	thymus
6	chr6:27788000-27791200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
7	chr6:27788000-27791200	Weak transcription	GM12878-XiMat	blood
8	chr6:27788000-27791400	Weak transcription	Duodenum Mucosa	Duodenum
9	chr6:27788000-27792000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
10	chr6:27788200-27792200	Weak transcription	A549	lung
11	chr6:27788400-27791200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
12	chr6:27789800-27791200	Weak transcription	Rectal Mucosa Donor 29	rectum
13	chr6:27790000-27791200	Weak transcription	Rectal Mucosa Donor 31	rectum
14	chr6:27790600-27791200	Enhancers	iPS-15b Cell Line	embryonic stem cell
15	chr6:27790600-27791400	Enhancers	Hela-S3	cervix
16	chr6:27790800-27791200	Enhancers	HUES64 Cell Line	embryonic stem cell
17	chr6:27790800-27791200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
18	chr6:27790800-27791200	Enhancers	Brain Germinal Matrix	brain
19	chr6:27791000-27791200	Enhancers	HUES6 Cell Line	embryonic stem cell
20	chr6:27791000-27791200	Enhancers	iPS-20b Cell Line	embryonic stem cell
21	chr6:27791000-27791200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
22	chr6:27791000-27791200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
23	chr6:27791000-27791200	Weak transcription	Primary neutrophils fromperipheralblood	blood
24	chr6:27791000-27791200	Enhancers	Primary B cells from cord blood	blood
25	chr6:27791000-27791200	Enhancers	Primary T cells from cord blood	blood
26	chr6:27791000-27791200	Enhancers	Primary hematopoietic stem cells	blood
27	chr6:27791000-27791200	Enhancers	Primary T helper naive cells from peripheral blood	blood
28	chr6:27791000-27791200	Enhancers	Primary T helper cells PMA-I stimulated	--
29	chr6:27791000-27791200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
30	chr6:27791000-27791200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
31	chr6:27791000-27791200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
32	chr6:27791000-27791200	Active TSS	Fetal Brain Female	brain
33	chr6:27791000-27791200	Enhancers	Fetal Intestine Small	intestine
34	chr6:27791000-27791200	Enhancers	Fetal Kidney	kidney
35	chr6:27791000-27791200	Enhancers	Fetal Lung	lung
36	chr6:27791000-27791200	Enhancers	HUVEC	blood vessel
37	chr6:27791000-27791200	Enhancers	Monocytes-CD14+_RO01746	blood
38	chr6:27791000-27791200	Enhancers	NH-A	brain
39	chr6:27791000-27791200	Enhancers	Osteobl	bone
40	chr6:27791000-27791400	Enhancers	HUES48 Cell Line	embryonic stem cell
41	chr6:27791000-27791400	Enhancers	iPS-18 Cell Line	embryonic stem cell
42	chr6:27791000-27791400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
43	chr6:27791000-27791400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
44	chr6:27791000-27791400	Enhancers	Fetal Heart	heart
45	chr6:27791000-27791400	Enhancers	HepG2	liver
46	chr6:27791000-27791600	Flanking Active TSS	Dnd41	blood
47	chr6:27791000-27792200	Active TSS	K562	blood
48	chr6:27791000-27793000	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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