Variant report

Variant	rs545453526
Chromosome Location	chr1:228289597-228289598
allele	A/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:12)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:228289389..228292049-chr1:228333496..228335357,2	K562	blood:
2	chr1:228284520..228292111-chr1:228324853..228335412,14	K562	blood:
3	chr1:228289424..228292369-chr1:228333748..228336393,2	MCF-7	breast:
4	chr1:228186714..228188137-chr1:228289568..228290450,5	MCF-7	breast:
5	chr1:228289288..228292230-chr1:228352223..228354730,2	MCF-7	breast:
6	chr1:228288459..228290327-chr1:228338206..228340411,2	K562	blood:
7	chr1:227921116..227923050-chr1:228289460..228292114,2	MCF-7	breast:
8	chr1:228288384..228298705-chr1:228351640..228357240,26	K562	blood:
9	chr1:228288054..228293498-chr1:228351743..228355627,9	K562	blood:
10	chr1:228286712..228292079-chr1:228327501..228330420,5	MCF-7	breast:
11	chr1:228288649..228293430-chr1:228325997..228329591,7	K562	blood:
12	chr1:228289454..228291459-chr1:228353037..228354863,4	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000203684	Chromatin interaction
ENSG00000081692	Chromatin interaction
ENSG00000143774	Chromatin interaction
ENSG00000181873	Chromatin interaction
ENSG00000143740	Chromatin interaction

Extended variants
information (count: 12 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:12 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1010605	chr1:227770415-228332690	Flanking Active TSS ZNF genes & repeats Weak transcription Strong transcription Genic enhancers Enhancers 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 miRNA miRNA target site	73 gene(s)	inside rSNPs	diseases
2	esv32853	chr1:227880116-228806209	Enhancers Genic enhancers Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Strong transcription Active TSS Flanking Active TSS 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	187 gene(s)	inside rSNPs	diseases
3	nsv427952	chr1:227881664-228308629	Flanking Active TSS Weak transcription ZNF genes & repeats Enhancers Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	61 gene(s)	inside rSNPs	diseases
4	nsv826908	chr1:227895386-228691100	Strong transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Weak transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	157 gene(s)	inside rSNPs	diseases
5	nsv516409	chr1:228035131-228296745	Enhancers Genic enhancers Active TSS Bivalent Enhancer Strong transcription Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
6	nsv523935	chr1:228038124-228681749	Enhancers Flanking Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription Weak transcription Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	137 gene(s)	inside rSNPs	diseases
7	nsv832803	chr1:228155118-228313681	Transcr. at gene 5' and 3' Weak transcription Active TSS Enhancers Flanking Active TSS Genic enhancers Bivalent Enhancer Strong transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
8	nsv873252	chr1:228174528-228371551	Strong transcription Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3' Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	85 gene(s)	inside rSNPs	diseases
9	nsv873253	chr1:228231601-228537942	Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	91 gene(s)	inside rSNPs	diseases
10	nsv873254	chr1:228231601-228543800	Weak transcription Genic enhancers Active TSS Enhancers Flanking Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	91 gene(s)	inside rSNPs	diseases
11	nsv873255	chr1:228254753-228684779	Genic enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Strong transcription Enhancers Active TSS 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	133 gene(s)	inside rSNPs	diseases
12	esv3425625	chr1:228289354-228292202	Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Weak transcription Strong transcription Genic enhancers Enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	11 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:126 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:228276800-228290200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr1:228277200-228290000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
3	chr1:228280800-228289600	Weak transcription	Small Intestine	intestine
4	chr1:228283800-228289600	Strong transcription	Brain Cingulate Gyrus	brain
5	chr1:228284200-228289600	Genic enhancers	Fetal Muscle Trunk	muscle
6	chr1:228287800-228290000	Weak transcription	Fetal Kidney	kidney
7	chr1:228288000-228290200	Weak transcription	Brain Substantia Nigra	brain
8	chr1:228288200-228289600	Weak transcription	Aorta	Aorta
9	chr1:228288200-228289600	Genic enhancers	Fetal Adrenal Gland	Adrenal Gland
10	chr1:228288200-228290000	Weak transcription	Left Ventricle	heart
11	chr1:228288600-228289600	Genic enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
12	chr1:228288600-228289600	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin02	Skin
13	chr1:228288600-228289600	Genic enhancers	Skeletal Muscle Female	skeletal muscle
14	chr1:228288600-228289600	Genic enhancers	Stomach Smooth Muscle	stomach
15	chr1:228288600-228289800	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin01	Skin
16	chr1:228288600-228289800	Genic enhancers	Right Ventricle	heart
17	chr1:228288600-228290400	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
18	chr1:228288800-228289600	Enhancers	Primary B cells from cord blood	blood
19	chr1:228288800-228289600	Genic enhancers	Brain Dorsolateral Prefrontal Cortex	brain
20	chr1:228288800-228289600	Enhancers	Placenta	Placenta
21	chr1:228288800-228290200	Enhancers	Fetal Heart	heart
22	chr1:228289000-228289600	Weak transcription	H9 Cell Line	embryonic stem cell
23	chr1:228289000-228289600	Transcr. at gene 5' and 3'	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr1:228289000-228289600	Weak transcription	HUES48 Cell Line	embryonic stem cell
25	chr1:228289000-228289600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
26	chr1:228289000-228289600	Weak transcription	Primary T cells from cord blood	blood
27	chr1:228289000-228289600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
28	chr1:228289000-228289600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
29	chr1:228289000-228289600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
30	chr1:228289000-228289600	Enhancers	Spleen	Spleen
31	chr1:228289000-228289600	Weak transcription	NHDF-Ad	bronchial
32	chr1:228289000-228289800	Enhancers	Liver	Liver
33	chr1:228289000-228289800	Enhancers	Placenta Amnion	Placenta Amnion
34	chr1:228289000-228290000	Weak transcription	Fetal Lung	lung
35	chr1:228289000-228290000	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
36	chr1:228289000-228290000	Weak transcription	HSMMtube	muscle
37	chr1:228289000-228290200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
38	chr1:228289000-228290400	Flanking Active TSS	Colonic Mucosa	Colon
39	chr1:228289200-228289600	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
40	chr1:228289200-228289600	Transcr. at gene 5' and 3'	Foreskin Keratinocyte Primary Cells skin03	Skin
41	chr1:228289200-228289600	Enhancers	Brain Angular Gyrus	brain
42	chr1:228289200-228289600	Genic enhancers	Colon Smooth Muscle	Colon
43	chr1:228289200-228289600	Genic enhancers	Fetal Stomach	stomach
44	chr1:228289200-228289600	Active TSS	Rectal Smooth Muscle	rectum
45	chr1:228289200-228289600	Flanking Active TSS	HepG2	liver
46	chr1:228289200-228289600	Enhancers	NH-A	brain
47	chr1:228289200-228289800	Enhancers	Primary B cells from peripheral blood	blood
48	chr1:228289200-228289800	Enhancers	Primary hematopoietic stem cells	blood
49	chr1:228289200-228289800	Genic enhancers	Brain Anterior Caudate	brain
50	chr1:228289200-228289800	Flanking Active TSS	Duodenum Smooth Muscle	Duodenum

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