Variant report

Variant	rs9608868
Chromosome Location	chr22:30696388-30696389
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr22:30692849..30696422-chr22:30721996..30724187,4	MCF-7	breast:
2	chr22:30692354..30698688-chr22:30699927..30704803,9	K562	blood:

Variant related genes	Relation type
ENSG00000099992	Chromatin interaction

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

rSNPs within LD-proxies of this variant (count:25)

rs_ID	r²[population]
rs34096486	0.85[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs3804077	1.00[AMR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs41281643	1.00[AMR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs41304671	1.00[AMR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs41308741	1.00[AMR][1000 genomes];0.82[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs9606713	1.00[AFR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9606715	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9606716	0.83[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs9606717	1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9606720	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9606727	1.00[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs9606730	1.00[AFR][1000 genomes]
rs9608862	1.00[AFR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9608865	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9608873	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9608876	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9608883	1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9608884	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9608886	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9608887	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9608897	0.85[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs9608900	0.85[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs9608902	0.85[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs9608905	0.85[AMR][1000 genomes]
rs9608906	0.85[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	nsv829171	chr22:30598030-31043578	Active TSS Weak transcription Flanking Active TSS Enhancers Genic enhancers Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	66 gene(s)	inside rSNPs	diseases
2	nsv914970	chr22:30619599-30850395	Active TSS Enhancers Genic enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	51 gene(s)	inside rSNPs	diseases
3	nsv834174	chr22:30619760-30746915	Enhancers Strong transcription Weak transcription Genic enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
4	nsv1062388	chr22:30649179-30711443	Strong transcription Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Active TSS Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
5	esv1799458	chr22:30659798-30698035	Weak transcription Enhancers Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:118 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr22:30686000-30700000	Weak transcription	Fetal Kidney	kidney
2	chr22:30686200-30720000	Weak transcription	Fetal Brain Male	brain
3	chr22:30686400-30701800	Weak transcription	HUES48 Cell Line	embryonic stem cell
4	chr22:30686600-30700600	Genic enhancers	Fetal Thymus	thymus
5	chr22:30686800-30701800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
6	chr22:30686800-30707200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
7	chr22:30687000-30699600	Strong transcription	Fetal Brain Female	brain
8	chr22:30687200-30697200	Weak transcription	H1 Cell Line	embryonic stem cell
9	chr22:30687400-30696400	Strong transcription	Monocytes-CD14+_RO01746	blood
10	chr22:30687400-30696600	Strong transcription	Primary monocytes fromperipheralblood	blood
11	chr22:30687400-30701200	Weak transcription	K562	blood
12	chr22:30687400-30706800	Weak transcription	HUES64 Cell Line	embryonic stem cell
13	chr22:30687600-30696400	Strong transcription	Primary neutrophils fromperipheralblood	blood
14	chr22:30687600-30697200	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
15	chr22:30687600-30699000	Weak transcription	HepG2	liver
16	chr22:30687600-30699800	Genic enhancers	Esophagus	oesophagus
17	chr22:30687600-30701400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
18	chr22:30687800-30696400	Weak transcription	NHDF-Ad	bronchial
19	chr22:30687800-30696600	Strong transcription	Primary hematopoietic stem cells short term culture	blood
20	chr22:30687800-30697600	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
21	chr22:30687800-30698000	Strong transcription	Osteobl	bone
22	chr22:30688000-30697400	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr22:30688000-30697400	Strong transcription	Duodenum Smooth Muscle	Duodenum
24	chr22:30688000-30697600	Weak transcription	HUVEC	blood vessel
25	chr22:30688200-30696400	Strong transcription	Adipose Nuclei	Adipose
26	chr22:30688200-30696800	Strong transcription	Duodenum Mucosa	Duodenum
27	chr22:30688200-30697200	Weak transcription	Brain Angular Gyrus	brain
28	chr22:30688200-30697200	Strong transcription	HSMMtube	muscle
29	chr22:30688200-30697800	Strong transcription	NHLF	lung
30	chr22:30688200-30698400	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
31	chr22:30688200-30698600	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
32	chr22:30688200-30699200	Strong transcription	Aorta	Aorta
33	chr22:30688200-30700600	Strong transcription	Fetal Stomach	stomach
34	chr22:30688400-30696800	Strong transcription	Fetal Muscle Leg	muscle
35	chr22:30688400-30697400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
36	chr22:30688400-30697800	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
37	chr22:30688400-30697800	Strong transcription	Liver	Liver
38	chr22:30688400-30698000	Strong transcription	GM12878-XiMat	blood
39	chr22:30688600-30697800	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
40	chr22:30689800-30698200	Weak transcription	A549	lung
41	chr22:30690200-30699000	Weak transcription	H9 Cell Line	embryonic stem cell
42	chr22:30690200-30700200	Genic enhancers	Primary T cells fromperipheralblood	blood
43	chr22:30690400-30698000	Genic enhancers	Primary T helper cells fromperipheralblood	blood
44	chr22:30690400-30700800	Weak transcription	HUES6 Cell Line	embryonic stem cell
45	chr22:30690800-30699800	Genic enhancers	Breast Myoepithelial Primary Cells	Breast
46	chr22:30690800-30701600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr22:30691000-30697800	Genic enhancers	Primary T helper naive cells from peripheral blood	blood
48	chr22:30691000-30706800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
49	chr22:30691400-30697200	Strong transcription	HSMM	muscle
50	chr22:30692000-30697600	Genic enhancers	Primary T helper 17 cells PMA-I stimulated	--

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