Variant report

Variant	rs60027965
Chromosome Location	chr8:8192960-8192961
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr8:8192658..8194970-chr8:8198409..8200233,2	K562	blood:
2	chr8:8191570..8193899-chr8:8241240..8244874,3	MCF-7	breast:
3	chr8:8191451..8193735-chr8:8198247..8200016,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000182319	Chromatin interaction

Extended variants
information (count: 56 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:38)

rs_ID	r²[population]
rs10099571	1.00[ASN][1000 genomes]
rs10101904	1.00[ASN][1000 genomes]
rs10110648	0.91[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs10110708	1.00[ASN][1000 genomes]
rs10503376	1.00[ASN][1000 genomes]
rs13248908	1.00[ASN][1000 genomes]
rs13259482	1.00[ASN][1000 genomes]
rs13439831	0.81[EUR][1000 genomes]
rs17604776	0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17607697	1.00[ASN][1000 genomes]
rs17664371	1.00[ASN][1000 genomes]
rs17669632	1.00[ASN][1000 genomes]
rs17670522	1.00[ASN][1000 genomes]
rs1914823	0.82[EUR][1000 genomes]
rs2102867	0.94[EUR][1000 genomes]
rs28756907	0.80[EUR][1000 genomes]
rs2976956	1.00[ASN][1000 genomes]
rs2976958	1.00[ASN][1000 genomes]
rs4840966	1.00[ASN][1000 genomes]
rs55817265	1.00[ASN][1000 genomes]
rs56097010	0.84[AMR][1000 genomes]
rs56735175	0.83[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs57837545	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6601693	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs66469655	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6991227	1.00[ASN][1000 genomes]
rs6998115	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7007943	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7013607	0.86[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs7014601	1.00[ASN][1000 genomes]
rs73184334	0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73184335	0.88[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs73184336	0.88[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs73184338	0.91[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs73184340	0.88[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs73199790	1.00[ASN][1000 genomes]
rs73523411	0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs882687	1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:18 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv915915	chr8:7239471-8222024	Enhancers Weak transcription Bivalent/Poised TSS Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	76 gene(s)	inside rSNPs	diseases
2	nsv533299	chr8:7268825-8222024	Flanking Bivalent TSS/Enh Weak transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Strong transcription Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	75 gene(s)	inside rSNPs	diseases
3	nsv869874	chr8:7753583-8229906	Enhancers Strong transcription Flanking Active TSS Weak transcription Genic enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	37 gene(s)	inside rSNPs	diseases
4	nsv817196	chr8:8079861-8255544	Weak transcription Genic enhancers Active TSS Enhancers Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
5	nsv890331	chr8:8093240-8971100	Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
6	nsv465448	chr8:8098079-8403142	Enhancers Flanking Active TSS Genic enhancers Weak transcription Strong transcription ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
7	nsv610152	chr8:8098079-8403142	Active TSS Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
8	nsv610153	chr8:8098079-8454531	Genic enhancers Strong transcription Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
9	nsv610154	chr8:8101641-8328101	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
10	nsv1032259	chr8:8108863-8247113	Strong transcription Active TSS Weak transcription Enhancers Flanking Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
11	nsv1020290	chr8:8108863-8260280	Bivalent Enhancer Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
12	nsv539440	chr8:8108863-8260280	Weak transcription Flanking Active TSS Enhancers Strong transcription ZNF genes & repeats Genic enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
13	nsv1025994	chr8:8108863-8580201	Enhancers Weak transcription Flanking Active TSS Strong transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
14	nsv1029268	chr8:8130629-8403435	Enhancers Strong transcription Flanking Active TSS Weak transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
15	nsv539446	chr8:8130629-8403435	Weak transcription Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
16	nsv1030433	chr8:8130629-8653691	Weak transcription Enhancers Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
17	nsv539447	chr8:8130629-8653691	Flanking Bivalent TSS/Enh Weak transcription Enhancers Flanking Active TSS Strong transcription Bivalent/Poised TSS ZNF genes & repeats Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
18	nsv610156	chr8:8163243-8207339	Weak transcription Genic enhancers Enhancers Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:120 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:8179600-8194600	Strong transcription	HepG2	liver
2	chr8:8182600-8196800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr8:8182800-8196200	Weak transcription	Rectal Smooth Muscle	rectum
4	chr8:8182800-8196400	Weak transcription	Aorta	Aorta
5	chr8:8182800-8215800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
6	chr8:8183000-8197000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr8:8183200-8199400	Strong transcription	HUES48 Cell Line	embryonic stem cell
8	chr8:8185600-8202200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr8:8185800-8195000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
10	chr8:8185800-8219600	Weak transcription	Ovary	ovary
11	chr8:8186400-8215800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
12	chr8:8187400-8195200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
13	chr8:8187600-8193000	Enhancers	Primary monocytes fromperipheralblood	blood
14	chr8:8187600-8193200	Enhancers	Primary B cells from peripheral blood	blood
15	chr8:8187800-8194000	Enhancers	Fetal Muscle Leg	muscle
16	chr8:8187800-8194200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
17	chr8:8188000-8194000	Enhancers	Brain Germinal Matrix	brain
18	chr8:8188000-8198800	Genic enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
19	chr8:8188400-8203800	Weak transcription	Colonic Mucosa	Colon
20	chr8:8188800-8195800	Weak transcription	Lung	lung
21	chr8:8189200-8193400	Weak transcription	K562	blood
22	chr8:8189200-8195000	Enhancers	Primary T killer memory cells from peripheral blood	blood
23	chr8:8189600-8203800	Weak transcription	Right Ventricle	heart
24	chr8:8190200-8194000	Enhancers	Skeletal Muscle Male	skeletal muscle
25	chr8:8190400-8193000	Enhancers	NHEK	skin
26	chr8:8190400-8193400	Enhancers	ES-I3 Cell Line	embryonic stem cell
27	chr8:8190600-8193000	Genic enhancers	HUES6 Cell Line	embryonic stem cell
28	chr8:8190800-8193000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
29	chr8:8190800-8193400	Flanking Active TSS	GM12878-XiMat	blood
30	chr8:8190800-8194600	Enhancers	Cortex derived primary cultured neurospheres	brain
31	chr8:8190800-8195400	Weak transcription	Esophagus	oesophagus
32	chr8:8191200-8193000	Enhancers	Primary T regulatory cells fromperipheralblood	blood
33	chr8:8191200-8195400	Weak transcription	Spleen	Spleen
34	chr8:8191400-8193600	Weak transcription	H9 Cell Line	embryonic stem cell
35	chr8:8191400-8193600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
36	chr8:8191600-8193200	Enhancers	Primary T cells from cord blood	blood
37	chr8:8191600-8193200	Weak transcription	Osteobl	bone
38	chr8:8191600-8193400	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr8:8191600-8193600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
40	chr8:8191600-8193800	Weak transcription	H1 Cell Line	embryonic stem cell
41	chr8:8191600-8193800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
42	chr8:8191600-8194000	Weak transcription	Liver	Liver
43	chr8:8191600-8194200	Enhancers	Fetal Brain Male	brain
44	chr8:8191600-8195000	Weak transcription	Fetal Stomach	stomach
45	chr8:8191600-8196200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
46	chr8:8191600-8196200	Weak transcription	Gastric	stomach
47	chr8:8191600-8196400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
48	chr8:8191600-8196400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
49	chr8:8191600-8200000	Weak transcription	Pancreas	Pancrea
50	chr8:8191600-8203600	Weak transcription	Brain Inferior Temporal Lobe	brain

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