Variant report

Variant	rs74356777
Chromosome Location	chr6:26341885-26341886
allele	C/G
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:25)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:25 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:26341882..26342492-chr6:26420774..26421520,2	MCF-7	breast:
2	chr6:26340033..26342028-chr6:26415409..26417011,2	MCF-7	breast:
3	chr6:26340332..26342039-chr6:26569832..26571583,2	K562	blood:
4	chr6:26338939..26342494-chr6:26519686..26522747,3	K562	blood:
5	chr6:26339658..26342406-chr6:26483476..26486207,2	K562	blood:
6	chr6:26340224..26342444-chr6:26572464..26573981,2	K562	blood:
7	chr6:26341837..26342412-chr6:26411698..26412292,2	MCF-7	breast:
8	chr6:26340823..26342973-chr6:26490879..26493737,2	K562	blood:
9	chr6:26338579..26343405-chr6:26519686..26522615,5	K562	blood:
10	chr6:26339036..26342767-chr6:26596200..26598139,3	K562	blood:
11	chr6:26340367..26342068-chr6:26565730..26567496,2	K562	blood:
12	chr6:26272455..26274796-chr6:26340559..26343243,3	MCF-7	breast:
13	chr6:26340224..26344158-chr6:26569567..26573981,6	K562	blood:
14	chr6:26339310..26342101-chr6:26554337..26555953,2	K562	blood:
15	chr6:26323184..26324056-chr6:26341539..26342363,2	K562	blood:
16	chr6:26341496..26342438-chr6:26493055..26494222,5	K562	blood:
17	chr6:26341541..26342734-chr6:26595701..26596713,9	K562	blood:
18	chr6:26341191..26342496-chr6:26493295..26494195,4	MCF-7	breast:
19	chr6:26341478..26343917-chr6:26362438..26365038,2	K562	blood:
20	chr6:26340127..26342724-chr6:26570668..26572890,2	MCF-7	breast:
21	chr6:26341264..26342451-chr6:26569043..26570054,3	K562	blood:
22	chr6:26340614..26342213-chr6:26550720..26552761,2	K562	blood:
23	chr6:26341644..26342483-chr6:26450003..26451206,4	MCF-7	breast:
24	chr6:26341150..26343678-chr6:26575652..26577197,2	K562	blood:
25	chr6:26341603..26342500-chr6:26520725..26521500,3	K562	blood:

No data

Variant related genes	Relation type
ENSG00000199289	Chromatin interaction
ENSG00000218690	Chromatin interaction
ENSG00000146109	Chromatin interaction
ENSG00000228223	Chromatin interaction
ENSG00000168242	Chromatin interaction

Extended variants
information (count: 11 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1029920	chr6:25638507-26585842	Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Enhancers Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Active TSS Genic enhancers Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	1215 gene(s)	inside rSNPs	diseases
2	nsv538162	chr6:25638507-26585842	Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	1215 gene(s)	inside rSNPs	diseases
3	nsv1030351	chr6:25813178-26352046	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1189 gene(s)	inside rSNPs	diseases
4	nsv1023453	chr6:25853830-26528250	Weak transcription Flanking Active TSS Enhancers Active TSS Bivalent/Poised TSS Strong transcription Genic enhancers Bivalent Enhancer 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	1201 gene(s)	inside rSNPs	diseases
5	nsv428137	chr6:25987413-26351920	Enhancers Flanking Active TSS Active TSS Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1181 gene(s)	inside rSNPs	diseases
6	nsv1018665	chr6:26026870-26352046	Flanking Active TSS Weak transcription Active TSS Enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1116 gene(s)	inside rSNPs	diseases
7	nsv482729	chr6:26291011-26470898	Weak transcription Active TSS Flanking Active TSS Enhancers Strong transcription Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	45 gene(s)	inside rSNPs	diseases
8	nsv5230	chr6:26321593-26361531	Weak transcription Bivalent Enhancer Flanking Active TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	32 gene(s)	inside rSNPs	diseases
9	esv3521788	chr6:26334022-26356973	Flanking Active TSS Weak transcription Enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
10	esv3521789	chr6:26334022-26356973	Weak transcription Bivalent Enhancer Enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
11	nsv601174	chr6:26341301-26350938	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:62 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:26333000-26342200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr6:26337000-26342000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
3	chr6:26337200-26342000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr6:26337200-26342000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
5	chr6:26337200-26342000	Weak transcription	Primary T helper cells fromperipheralblood	blood
6	chr6:26337400-26342000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr6:26337400-26342000	Weak transcription	Monocytes-CD14+_RO01746	blood
8	chr6:26337400-26342200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
9	chr6:26337400-26342200	Weak transcription	NHDF-Ad	bronchial
10	chr6:26337600-26342200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
11	chr6:26337600-26342200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr6:26337600-26342200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
13	chr6:26337600-26342200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
14	chr6:26337600-26342200	Weak transcription	HUVEC	blood vessel
15	chr6:26337600-26342200	Enhancers	K562	blood
16	chr6:26337600-26342200	Weak transcription	NHEK	skin
17	chr6:26337600-26342200	Weak transcription	NHLF	lung
18	chr6:26337800-26342200	Weak transcription	HMEC	breast
19	chr6:26340200-26342000	Weak transcription	NH-A	brain
20	chr6:26341400-26342000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
21	chr6:26341400-26342000	Enhancers	Hela-S3	cervix
22	chr6:26341400-26342200	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
23	chr6:26341400-26343000	Active TSS	HUES64 Cell Line	embryonic stem cell
24	chr6:26341600-26342000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
25	chr6:26341600-26342000	Enhancers	Primary T cells fromperipheralblood	blood
26	chr6:26341600-26342000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
27	chr6:26341600-26342000	Enhancers	Fetal Thymus	thymus
28	chr6:26341600-26342600	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
29	chr6:26341600-26342800	Active TSS	iPS-18 Cell Line	embryonic stem cell
30	chr6:26341600-26342800	Flanking Active TSS	HepG2	liver
31	chr6:26341600-26343000	Active TSS	iPS-15b Cell Line	embryonic stem cell
32	chr6:26341600-26343200	Active TSS	HUES6 Cell Line	embryonic stem cell
33	chr6:26341800-26342000	Flanking Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
34	chr6:26341800-26342000	Active TSS	Primary T regulatory cells fromperipheralblood	blood
35	chr6:26341800-26342000	Bivalent Enhancer	Brain Germinal Matrix	brain
36	chr6:26341800-26342000	Enhancers	Brain Hippocampus Middle	brain
37	chr6:26341800-26342000	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
38	chr6:26341800-26342000	Enhancers	Right Atrium	heart
39	chr6:26341800-26342000	Flanking Active TSS	Stomach Smooth Muscle	stomach
40	chr6:26341800-26342000	Flanking Active TSS	GM12878-XiMat	blood
41	chr6:26341800-26342200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
42	chr6:26341800-26342200	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
43	chr6:26341800-26342200	Enhancers	Brain Angular Gyrus	brain
44	chr6:26341800-26342200	Bivalent Enhancer	Fetal Muscle Leg	muscle
45	chr6:26341800-26342200	Bivalent Enhancer	Fetal Stomach	stomach
46	chr6:26341800-26342400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
47	chr6:26341800-26342400	Enhancers	Primary monocytes fromperipheralblood	blood
48	chr6:26341800-26342400	Enhancers	Primary B cells from peripheral blood	blood
49	chr6:26341800-26342400	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
50	chr6:26341800-26342400	Enhancers	Esophagus	oesophagus

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