Variant report

Variant	rs73026359
Chromosome Location	chr1:153523682-153523683
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:7)
CpG islands
(count:0)
Chromatin interactive
region (count:7)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:7 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	SPI1	chr1:153523672-153523783	K562	blood:	n/a	n/a
2	POLR2A	chr1:153522989-153525739	K562	blood:	n/a	n/a
3	BHLHE40	chr1:153523661-153523884	K562	blood:	n/a	n/a
4	RUNX3	chr1:153523292-153523738	GM12878	blood:	n/a	n/a
5	POLR2A	chr1:153517452-153526571	MCF10A-Er-Src	breast:	n/a	n/a
6	SPI1	chr1:153523571-153523920	HL-60	blood:	n/a	n/a
7	SPI1	chr1:153523554-153524060	HL-60	blood:	n/a	n/a

No data

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:153508236..153509740-chr1:153522237..153524623,2	K562	blood:
2	chr1:153522864..153527279-chr1:153528529..153531164,4	K562	blood:
3	chr1:153523096..153524724-chr1:153583909..153585635,2	MCF-7	breast:
4	chr1:153514728..153519163-chr1:153523629..153528346,5	K562	blood:
5	chr1:153522267..153525133-chr1:153537337..153540137,3	MCF-7	breast:
6	chr1:153511594..153513474-chr1:153523017..153524733,2	K562	blood:
7	chr1:153504382..153507280-chr1:153522086..153523762,2	K562	blood:

No data

Variant related genes	Relation type
S100A3	TF binding region
S100A4	TF binding region
ENSG00000188643	Chromatin interaction
ENSG00000196420	Chromatin interaction
ENSG00000238279	Chromatin interaction
ENSG00000197956	Chromatin interaction
ENSG00000196754	Chromatin interaction
ENSG00000196154	Chromatin interaction

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

rSNPs within LD-proxies of this variant (count:6)

rs_ID	r²[population]
rs59462422	0.84[AFR][1000 genomes]
rs61522372	0.84[AFR][1000 genomes]
rs73009915	0.89[AFR][1000 genomes]
rs73026343	1.00[AFR][1000 genomes]
rs73026360	0.84[AFR][1000 genomes]
rs73026363	0.84[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1010488	chr1:152901263-153670972	Genic enhancers Active TSS Strong transcription Bivalent/Poised TSS Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	236 gene(s)	inside rSNPs	diseases
2	nsv535171	chr1:152901263-153670972	Enhancers Flanking Active TSS Weak transcription Genic enhancers Bivalent Enhancer Strong transcription Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	236 gene(s)	inside rSNPs	diseases
3	nsv1002705	chr1:153307852-153525589	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	152 gene(s)	inside rSNPs	diseases
4	nsv831603	chr1:153405842-153576143	Transcr. at gene 5' and 3' Bivalent Enhancer Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	148 gene(s)	inside rSNPs	diseases
5	nsv1007306	chr1:153413827-153541798	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	146 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:73 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:153509400-153527600	Enhancers	Breast Myoepithelial Primary Cells	Breast
2	chr1:153517400-153524000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr1:153518200-153524000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
4	chr1:153518200-153524000	Enhancers	K562	blood
5	chr1:153518400-153523800	Enhancers	ES-I3 Cell Line	embryonic stem cell
6	chr1:153518600-153524000	Enhancers	HUES6 Cell Line	embryonic stem cell
7	chr1:153518600-153524000	Enhancers	Placenta	Placenta
8	chr1:153518600-153524200	Enhancers	Lung	lung
9	chr1:153518800-153524200	Enhancers	Esophagus	oesophagus
10	chr1:153519000-153524400	Enhancers	Primary monocytes fromperipheralblood	blood
11	chr1:153519200-153524000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr1:153519200-153524200	Genic enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
13	chr1:153519200-153524400	Enhancers	Primary hematopoietic stem cells short term culture	blood
14	chr1:153519400-153526000	Weak transcription	Aorta	Aorta
15	chr1:153520000-153529400	Genic enhancers	HMEC	breast
16	chr1:153520200-153524200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
17	chr1:153520400-153524200	Enhancers	Adipose Nuclei	Adipose
18	chr1:153521200-153524000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
19	chr1:153521400-153524200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
20	chr1:153521400-153524400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
21	chr1:153521800-153525600	Weak transcription	Fetal Heart	heart
22	chr1:153521800-153526400	Weak transcription	Duodenum Mucosa	Duodenum
23	chr1:153522000-153525600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
24	chr1:153522200-153523800	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin02	Skin
25	chr1:153522200-153524000	Enhancers	Primary B cells from cord blood	blood
26	chr1:153522200-153524000	Genic enhancers	NHEK	skin
27	chr1:153522200-153525600	Weak transcription	Ovary	ovary
28	chr1:153522400-153524000	Weak transcription	Rectal Mucosa Donor 31	rectum
29	chr1:153522400-153524000	Enhancers	A549	lung
30	chr1:153522400-153525800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
31	chr1:153522400-153526200	Weak transcription	Rectal Smooth Muscle	rectum
32	chr1:153522400-153526200	Weak transcription	Stomach Mucosa	stomach
33	chr1:153522600-153524200	Enhancers	Primary hematopoietic stem cells	blood
34	chr1:153522600-153524200	Genic enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
35	chr1:153522600-153524200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
36	chr1:153522600-153525600	Weak transcription	Muscle Satellite Cultured Cells	--
37	chr1:153522600-153525800	Weak transcription	Osteobl	bone
38	chr1:153522600-153526000	Weak transcription	HUVEC	blood vessel
39	chr1:153522600-153526200	Weak transcription	NH-A	brain
40	chr1:153522600-153526400	Weak transcription	Fetal Stomach	stomach
41	chr1:153522600-153526400	Weak transcription	Pancreas	Pancrea
42	chr1:153522600-153538000	Weak transcription	Colonic Mucosa	Colon
43	chr1:153522800-153524800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
44	chr1:153522800-153524800	Weak transcription	NHLF	lung
45	chr1:153522800-153525600	Weak transcription	Spleen	Spleen
46	chr1:153522800-153525800	Enhancers	HepG2	liver
47	chr1:153522800-153526000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
48	chr1:153522800-153526000	Weak transcription	Colon Smooth Muscle	Colon
49	chr1:153522800-153526000	Weak transcription	Duodenum Smooth Muscle	Duodenum
50	chr1:153522800-153526000	Weak transcription	Right Ventricle	heart

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