Variant report

Variant	rs478934
Chromosome Location	chr6:76325096-76325097
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	KAP1	chr6:76324366-76325344	HEK293	kidney:	n/a	n/a
2	CEBPB	chr6:76325006-76325223	IMR90	lung:	n/a	n/a
3	CEBPB	chr6:76324961-76325231	K562	blood:	n/a	n/a
4	SETDB1	chr6:76324571-76325398	U2OS	brain:	n/a	n/a
5	CEBPB	chr6:76324962-76325213	Hela-S3	cervix:	n/a	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:76313605..76316318-chr6:76324603..76327531,2	MCF-7	breast:
2	chr6:76309815..76313106-chr6:76322931..76328588,7	MCF-7	breast:

Variant related genes	Relation type
ENSG00000217488	TF binding region
ENSG00000112701	Chromatin interaction

Extended variants
information (count: 53 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:32)

rs_ID	r²[population]
rs1018103	0.92[AFR][1000 genomes];0.82[AMR][1000 genomes];0.87[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs10943273	0.84[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs10943274	0.83[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs12199457	0.88[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs12524436	0.88[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs12525161	0.85[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs13191639	0.86[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs2133192	0.92[AFR][1000 genomes];0.86[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2647415	0.92[AFR][1000 genomes];0.84[AMR][1000 genomes];0.88[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2647416	0.82[AFR][1000 genomes];0.82[AMR][1000 genomes];0.86[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs34239015	0.88[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs486777	0.84[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs570939	0.88[AFR][1000 genomes];0.84[AMR][1000 genomes];0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs575720	0.88[AFR][1000 genomes];0.98[AMR][1000 genomes];0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6453832	0.81[AFR][1000 genomes];0.92[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs649935	0.87[AFR][1000 genomes];0.98[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6907247	0.90[AFR][1000 genomes];0.82[AMR][1000 genomes];0.87[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6911868	0.83[AFR][1000 genomes];0.85[AMR][1000 genomes];0.85[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6936251	0.83[AFR][1000 genomes];0.85[AMR][1000 genomes];0.85[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6936565	0.90[AFR][1000 genomes];0.86[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7356806	0.82[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs7747801	0.84[AMR][1000 genomes];0.81[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs775071	0.89[AFR][1000 genomes];0.82[AMR][1000 genomes];0.87[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs9294001	0.82[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs9350598	0.86[AFR][1000 genomes];0.85[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs9352237	0.90[AFR][1000 genomes];0.87[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs9352238	0.92[AFR][1000 genomes];0.86[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs9359137	0.89[AFR][1000 genomes];0.86[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs9447522	0.88[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs9447523	0.88[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs9447524	0.88[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs9885866	0.88[AMR][1000 genomes];0.82[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:21 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1027915	chr6:75893542-76510113	Active TSS Enhancers Strong transcription Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	70 gene(s)	inside rSNPs	diseases
2	nsv538311	chr6:75893542-76510113	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Strong transcription Bivalent/Poised TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	70 gene(s)	inside rSNPs	diseases
3	nsv1022428	chr6:76023118-76575620	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	48 gene(s)	inside rSNPs	diseases
4	nsv538312	chr6:76023118-76575620	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Active TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	48 gene(s)	inside rSNPs	diseases
5	nsv1032245	chr6:76045537-76545703	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	47 gene(s)	inside rSNPs	diseases
6	nsv538313	chr6:76045537-76545703	Strong transcription Weak transcription Enhancers Active TSS Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	47 gene(s)	inside rSNPs	diseases
7	nsv1019328	chr6:76154751-76604197	Enhancers Weak transcription Strong transcription Active TSS Bivalent/Poised TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	44 gene(s)	inside rSNPs	diseases
8	nsv538314	chr6:76154751-76604197	Enhancers Strong transcription Active TSS Weak transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	44 gene(s)	inside rSNPs	diseases
9	nsv1023331	chr6:76238459-76482117	Strong transcription ZNF genes & repeats Active TSS Weak transcription Flanking Active TSS Enhancers Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	38 gene(s)	inside rSNPs	diseases
10	nsv538315	chr6:76238459-76482117	Enhancers Strong transcription Flanking Active TSS Weak transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	38 gene(s)	inside rSNPs	diseases
11	nsv1017542	chr6:76238459-76537447	Strong transcription Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	38 gene(s)	inside rSNPs	diseases
12	nsv1031745	chr6:76257913-76493355	Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Strong transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	38 gene(s)	inside rSNPs	diseases
13	nsv538316	chr6:76257913-76493355	Strong transcription Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	38 gene(s)	inside rSNPs	diseases
14	nsv533100	chr6:76257914-76493354	Enhancers Weak transcription Strong transcription Genic enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	38 gene(s)	inside rSNPs	diseases
15	nsv1023749	chr6:76287578-76482117	Weak transcription Flanking Active TSS Genic enhancers Strong transcription Enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	38 gene(s)	inside rSNPs	diseases
16	nsv538317	chr6:76287578-76482117	Strong transcription Weak transcription Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	38 gene(s)	inside rSNPs	diseases
17	nsv1021090	chr6:76306100-76759397	Weak transcription Enhancers Active TSS Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
18	nsv538318	chr6:76306100-76759397	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Bivalent/Poised TSS Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
19	nsv886183	chr6:76320846-76399539	Strong transcription Enhancers Weak transcription Genic enhancers ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
20	nsv886184	chr6:76320846-76462711	Weak transcription Strong transcription Flanking Active TSS Enhancers Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
21	nsv886185	chr6:76320846-76498109	Weak transcription Strong transcription Flanking Active TSS Enhancers ZNF genes & repeats Active TSS Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs478934	SENP6	cis	Whole Blood	GTEx

Chromatin state (count:104 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:76313800-76325400	Enhancers	Primary monocytes fromperipheralblood	blood
2	chr6:76313800-76331600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr6:76314000-76325600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
4	chr6:76314000-76325800	Enhancers	Primary T killer memory cells from peripheral blood	blood
5	chr6:76314000-76326000	Enhancers	Primary T helper cells fromperipheralblood	blood
6	chr6:76314000-76343200	Weak transcription	Fetal Kidney	kidney
7	chr6:76314200-76325200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
8	chr6:76314200-76325200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
9	chr6:76314200-76329000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
10	chr6:76314400-76327600	Weak transcription	Cortex derived primary cultured neurospheres	brain
11	chr6:76314400-76334800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr6:76314400-76336800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
13	chr6:76316400-76326000	Enhancers	Colon Smooth Muscle	Colon
14	chr6:76317600-76327400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr6:76318200-76334800	Weak transcription	Fetal Muscle Trunk	muscle
16	chr6:76319000-76329200	Weak transcription	Fetal Lung	lung
17	chr6:76319800-76333400	Weak transcription	HMEC	breast
18	chr6:76319800-76348400	Weak transcription	NHEK	skin
19	chr6:76320000-76329200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
20	chr6:76320200-76325200	Enhancers	Stomach Mucosa	stomach
21	chr6:76320200-76333200	Weak transcription	NH-A	brain
22	chr6:76320200-76351800	Weak transcription	HSMMtube	muscle
23	chr6:76320200-76391600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
24	chr6:76320600-76327800	Weak transcription	Brain Angular Gyrus	brain
25	chr6:76320600-76330000	Weak transcription	Brain Inferior Temporal Lobe	brain
26	chr6:76320800-76327200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
27	chr6:76320800-76334400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
28	chr6:76321200-76348400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
29	chr6:76321400-76328200	Weak transcription	Stomach Smooth Muscle	stomach
30	chr6:76321600-76329000	Weak transcription	Brain Cingulate Gyrus	brain
31	chr6:76321600-76331600	Weak transcription	HUES48 Cell Line	embryonic stem cell
32	chr6:76321600-76332800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
33	chr6:76321600-76334000	Weak transcription	HSMM	muscle
34	chr6:76321600-76339400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
35	chr6:76321800-76370400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
36	chr6:76322000-76341600	Weak transcription	NHLF	lung
37	chr6:76322400-76328200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
38	chr6:76322400-76329400	Weak transcription	Right Ventricle	heart
39	chr6:76322600-76325600	Enhancers	Primary T helper naive cells from peripheral blood	blood
40	chr6:76322600-76326200	Enhancers	Primary T helper cells PMA-I stimulated	--
41	chr6:76322600-76328400	Weak transcription	Dnd41	blood
42	chr6:76322600-76329400	Weak transcription	Aorta	Aorta
43	chr6:76322600-76361000	Weak transcription	Thymus	Thymus
44	chr6:76322800-76326200	Weak transcription	Pancreas	Pancrea
45	chr6:76322800-76329400	Weak transcription	Lung	lung
46	chr6:76322800-76333800	Weak transcription	Placenta	Placenta
47	chr6:76323200-76325200	Enhancers	Monocytes-CD14+_RO01746	blood
48	chr6:76323200-76325400	Weak transcription	Brain Substantia Nigra	brain
49	chr6:76323200-76326600	Weak transcription	Psoas Muscle	Psoas
50	chr6:76323200-76327600	Weak transcription	Breast Myoepithelial Primary Cells	Breast

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