Variant report

Variant	rs41270076
Chromosome Location	chr6:35467891-35467892
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:8)
CpG islands
(count:0)
Chromatin interactive
region (count:6)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:8 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr6:35467531-35467992	K562	blood:	n/a	n/a
2	POLR2A	chr6:35465558-35468992	K562	blood:	n/a	n/a
3	POLR2A	chr6:35467401-35468289	K562	blood:	n/a	n/a
4	POLR2A	chr6:35467463-35468303	Hela-S3	cervix:	n/a	n/a
5	POLR2A	chr6:35464413-35468773	H1-hESC	embryonic stem cell:	n/a	n/a
6	POLR2A	chr6:35467457-35468203	ECC-1	luminal epithelium:	n/a	n/a
7	POLR2A	chr6:35467794-35468034	MCF-7	breast:	n/a	n/a
8	POLR2A	chr6:35467308-35468376	H1-hESC	embryonic stem cell:	n/a	n/a

No data

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

No.	Distal block	Cell Line	Cell type
1	chr6:35423795..35426623-chr6:35465037..35468781,3	K562	blood:
2	chr6:35465446..35468035-chr6:35607430..35610345,2	K562	blood:
3	chr6:35264944..35267460-chr6:35465302..35468823,3	MCF-7	breast:
4	chr6:35464601..35467910-chr6:35655207..35659461,3	K562	blood:
5	chr6:35418643..35423313-chr6:35462563..35468017,10	K562	blood:
6	chr6:35465886..35468037-chr6:35705048..35706925,2	K562	blood:

No data

Variant related genes	Relation type
TEAD3	TF binding region
ENSG00000023892	Chromatin interaction
ENSG00000112039	Chromatin interaction
ENSG00000096060	Chromatin interaction

Extended variants
information (count: 14 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs2395627	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs57265953	1.00[EUR][1000 genomes]
rs6903482	1.00[EUR][1000 genomes]
rs6906095	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7743057	0.87[AMR][1000 genomes]
rs7759599	1.00[EUR][1000 genomes]
rs7770128	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv519370	chr6:35378778-35537406	Weak transcription Bivalent Enhancer Enhancers Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	72 gene(s)	inside rSNPs	diseases
2	nsv984463	chr6:35432948-35477634	Weak transcription Enhancers Strong transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region miRNA	67 gene(s)	inside rSNPs	diseases
3	nsv462909	chr6:35457396-35502202	Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Weak transcription Bivalent/Poised TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region	24 gene(s)	inside rSNPs	diseases
4	nsv602912	chr6:35457396-35502202	Enhancers Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	24 gene(s)	inside rSNPs	diseases
5	esv2758048	chr6:35463741-35806504	Genic enhancers Weak transcription Active TSS Bivalent Enhancer Enhancers Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	52 gene(s)	inside rSNPs	diseases
6	esv2759420	chr6:35463741-35806504	Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Enhancers Active TSS Bivalent Enhancer Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	52 gene(s)	inside rSNPs	diseases
7	esv1820663	chr6:35464197-35471362	Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Enhancers Active TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region	23 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:44 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:35465600-35469200	Enhancers	Fetal Heart	heart
2	chr6:35466000-35468800	Enhancers	Skeletal Muscle Female	skeletal muscle
3	chr6:35466400-35468000	Weak transcription	HSMM	muscle
4	chr6:35466400-35468000	Weak transcription	HSMMtube	muscle
5	chr6:35466400-35468200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr6:35466400-35468200	Weak transcription	Osteobl	bone
7	chr6:35466400-35468600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
8	chr6:35466400-35469200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr6:35466400-35469200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr6:35466400-35476800	Weak transcription	Cortex derived primary cultured neurospheres	brain
11	chr6:35466400-35479200	Weak transcription	Right Ventricle	heart
12	chr6:35466600-35468000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
13	chr6:35466600-35468400	Weak transcription	Muscle Satellite Cultured Cells	--
14	chr6:35466600-35468400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
15	chr6:35466600-35468400	Weak transcription	NHLF	lung
16	chr6:35466600-35469000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
17	chr6:35466800-35468000	Enhancers	Fetal Muscle Leg	muscle
18	chr6:35466800-35468200	Weak transcription	Hela-S3	cervix
19	chr6:35466800-35468600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
20	chr6:35466800-35468600	Weak transcription	NH-A	brain
21	chr6:35466800-35477000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr6:35466800-35479400	Weak transcription	Right Atrium	heart
23	chr6:35467000-35468000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
24	chr6:35467000-35468000	Weak transcription	NHDF-Ad	bronchial
25	chr6:35467000-35468200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
26	chr6:35467000-35468400	Weak transcription	H9 Cell Line	embryonic stem cell
27	chr6:35467000-35473400	Weak transcription	Esophagus	oesophagus
28	chr6:35467200-35468200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
29	chr6:35467200-35468400	Weak transcription	Fetal Stomach	stomach
30	chr6:35467200-35469400	Enhancers	Placenta	Placenta
31	chr6:35467400-35468400	Weak transcription	K562	blood
32	chr6:35467400-35478600	Weak transcription	Fetal Lung	lung
33	chr6:35467600-35468000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
34	chr6:35467600-35468000	Weak transcription	Placenta Amnion	Placenta Amnion
35	chr6:35467600-35468400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
36	chr6:35467600-35469200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
37	chr6:35467600-35469200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr6:35467600-35469200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
39	chr6:35467600-35471600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
40	chr6:35467800-35468000	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
41	chr6:35467800-35468000	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
42	chr6:35467800-35468600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
43	chr6:35467800-35469200	Enhancers	Left Ventricle	heart
44	chr6:35467800-35469200	Enhancers	Psoas Muscle	Psoas

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