Variant report

Variant	rs12073045
Chromosome Location	chr1:45990978-45990979
allele	G/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	SPI1	chr1:45990747-45991033	K562	blood:	n/a	chr1:45990879-45990892 chr1:45990881-45990890 chr1:45990878-45990891
2	SPI1	chr1:45990750-45990991	K562	blood:	n/a	chr1:45990879-45990892 chr1:45990881-45990890 chr1:45990878-45990891
3	SPI1	chr1:45990648-45991151	HL-60	blood:	n/a	chr1:45990879-45990892 chr1:45990881-45990890 chr1:45990878-45990891
4	SPI1	chr1:45990649-45991156	HL-60	blood:	n/a	chr1:45990879-45990892 chr1:45990881-45990890 chr1:45990878-45990891
5	BACH1	chr1:45990739-45991030	H1-hESC	embryonic stem cell:	n/a	n/a
6	MAFK	chr1:45990676-45991088	H1-hESC	embryonic stem cell:	n/a	n/a
7	SPI1	chr1:45990650-45991008	GM12891	blood:	n/a	chr1:45990879-45990892 chr1:45990881-45990890 chr1:45990878-45990891
8	EP300	chr1:45990610-45991193	A549	lung:	n/a	n/a
9	SPI1	chr1:45990707-45991001	GM12891	blood:	n/a	chr1:45990879-45990892 chr1:45990881-45990890 chr1:45990878-45990891

No.	Distal block	Cell Line	Cell type
1	chr1:45990085..45992504-chr1:45996653..45999903,3	MCF-7	breast:
2	chr1:45805140..45807328-chr1:45987853..45992059,3	K562	blood:
3	chr1:45990878..45992460-chr1:46016513..46018764,2	K562	blood:
4	chr1:45990201..45992328-chr1:46015000..46016873,3	MCF-7	breast:
5	chr1:45984791..45989119-chr1:45989451..45994043,12	MCF-7	breast:
6	chr1:45985569..45992282-chr1:46014173..46025125,38	MCF-7	breast:
7	chr1:45990531..45992358-chr1:46014805..46016386,2	K562	blood:
8	chr1:45982844..45990993-chr1:46030121..46038313,25	K562	blood:
9	chr1:45980210..45995142-chr1:46046095..46057139,89	K562	blood:
10	chr1:45284051..45285694-chr1:45989373..45992080,2	K562	blood:
11	chr1:45974558..45995867-chr1:46046173..46057010,94	K562	blood:
12	chr1:45826987..45828662-chr1:45989193..45991039,2	K562	blood:

Variant related genes	Relation type
PRDX1	TF binding region
ENSG00000202444	Chromatin interaction
ENSG00000132780	Chromatin interaction
ENSG00000117450	Chromatin interaction
ENSG00000132773	Chromatin interaction
ENSG00000132781	Chromatin interaction
ENSG00000117448	Chromatin interaction

Extended variants
information (count: 64 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:56)

rs_ID	r²[population]
rs11211127	1.00[AMR][1000 genomes]
rs11211144	1.00[AMR][1000 genomes]
rs11211148	1.00[AMR][1000 genomes]
rs11211153	1.00[AMR][1000 genomes]
rs11211154	1.00[AMR][1000 genomes]
rs11211155	1.00[AMR][1000 genomes]
rs11211156	1.00[AMR][1000 genomes]
rs11211167	1.00[AMR][1000 genomes]
rs12057167	1.00[AMR][1000 genomes]
rs12060056	1.00[AMR][1000 genomes]
rs12061890	1.00[AMR][1000 genomes]
rs12063380	1.00[AMR][1000 genomes]
rs12064908	1.00[AMR][1000 genomes]
rs12067882	1.00[AMR][1000 genomes]
rs12070146	1.00[AMR][1000 genomes]
rs12070177	1.00[AMR][1000 genomes]
rs12073047	1.00[AMR][1000 genomes]
rs12073132	1.00[AMR][1000 genomes]
rs12077112	1.00[AMR][1000 genomes]
rs12080482	1.00[AMR][1000 genomes]
rs12081121	1.00[AMR][1000 genomes]
rs12082672	1.00[AMR][1000 genomes]
rs12085372	1.00[AMR][1000 genomes]
rs12086880	1.00[AMR][1000 genomes]
rs12088810	1.00[AMR][1000 genomes]
rs12091335	1.00[AMR][1000 genomes]
rs12091360	1.00[AMR][1000 genomes]
rs12093444	1.00[AMR][1000 genomes]
rs12094011	1.00[AMR][1000 genomes]
rs12097914	1.00[AMR][1000 genomes]
rs16832540	1.00[AMR][1000 genomes]
rs16832550	1.00[AMR][1000 genomes]
rs16832553	1.00[AMR][1000 genomes]
rs16832557	1.00[AMR][1000 genomes]
rs1691225	1.00[AMR][1000 genomes]
rs1691226	1.00[AMR][1000 genomes]
rs1691227	1.00[AMR][1000 genomes]
rs1762087	1.00[AMR][1000 genomes]
rs2782489	1.00[AMR][1000 genomes]
rs28532613	1.00[AMR][1000 genomes]
rs28548585	1.00[AMR][1000 genomes]
rs28576912	1.00[AMR][1000 genomes]
rs28607905	1.00[AMR][1000 genomes]
rs35067820	1.00[AMR][1000 genomes]
rs35808563	1.00[AMR][1000 genomes]
rs486346	1.00[AMR][1000 genomes]
rs505175	1.00[AMR][1000 genomes]
rs506094	1.00[AMR][1000 genomes]
rs525706	1.00[AMR][1000 genomes]
rs622296	1.00[AMR][1000 genomes]
rs635446	1.00[AMR][1000 genomes]
rs665014	1.00[AMR][1000 genomes]
rs668289	1.00[AMR][1000 genomes]
rs669417	1.00[AMR][1000 genomes]
rs680267	1.00[AMR][1000 genomes]
rs7550744	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv498036	chr1:45428030-46050934	Active TSS Enhancers Flanking Active TSS Genic enhancers Weak transcription Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	191 gene(s)	inside rSNPs	diseases
2	esv1795802	chr1:45819489-46009818	Enhancers Weak transcription Active TSS Genic enhancers Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	126 gene(s)	inside rSNPs	diseases
3	esv1831217	chr1:45819489-46009818	Strong transcription Enhancers Genic enhancers Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	126 gene(s)	inside rSNPs	diseases
4	nsv530016	chr1:45868543-46069020	Flanking Active TSS Genic enhancers Weak transcription Active TSS Enhancers Transcr. at gene 5' and 3' Strong transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	149 gene(s)	inside rSNPs	diseases
5	nsv829726	chr1:45897581-46103186	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	148 gene(s)	inside rSNPs	diseases
6	nsv529631	chr1:45905936-46335246	Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Weak transcription Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	207 gene(s)	inside rSNPs	diseases
7	nsv932680	chr1:45935520-46686477	Strong transcription Weak transcription Flanking Active TSS Active TSS Enhancers Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	232 gene(s)	inside rSNPs	diseases
8	nsv868828	chr1:45953923-46686477	Active TSS Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	232 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:38 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:45988200-45991000	Enhancers	Dnd41	blood
2	chr1:45988200-45992200	Weak transcription	Fetal Lung	lung
3	chr1:45988200-45993000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr1:45988400-45992200	Weak transcription	Fetal Intestine Large	intestine
5	chr1:45988400-45992200	Weak transcription	Fetal Kidney	kidney
6	chr1:45988400-45993400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr1:45988400-45997200	Weak transcription	Monocytes-CD14+_RO01746	blood
8	chr1:45988600-45991000	Weak transcription	Liver	Liver
9	chr1:45988600-45992200	Weak transcription	Fetal Heart	heart
10	chr1:45988600-45992200	Weak transcription	Fetal Intestine Small	intestine
11	chr1:45988600-45993400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
12	chr1:45989000-45993200	Weak transcription	Placenta	Placenta
13	chr1:45989200-46000600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr1:45990200-45991000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
15	chr1:45990400-45991200	Enhancers	Primary hematopoietic stem cells short term culture	blood
16	chr1:45990400-45992400	Enhancers	Hela-S3	cervix
17	chr1:45990400-45992600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
18	chr1:45990400-45992600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
19	chr1:45990600-45991000	Enhancers	ES-I3 Cell Line	embryonic stem cell
20	chr1:45990600-45991000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
21	chr1:45990600-45991000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
22	chr1:45990600-45991000	Enhancers	HUES48 Cell Line	embryonic stem cell
23	chr1:45990600-45991000	Enhancers	HUES64 Cell Line	embryonic stem cell
24	chr1:45990600-45991000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
25	chr1:45990600-45991000	Enhancers	K562	blood
26	chr1:45990600-45991200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr1:45990600-45991200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr1:45990600-45991200	Enhancers	HUES6 Cell Line	embryonic stem cell
29	chr1:45990600-45991200	Enhancers	iPS-15b Cell Line	embryonic stem cell
30	chr1:45990600-45991200	Enhancers	iPS-20b Cell Line	embryonic stem cell
31	chr1:45990600-45991200	Enhancers	HSMMtube	muscle
32	chr1:45990600-45992200	Enhancers	iPS-18 Cell Line	embryonic stem cell
33	chr1:45990600-45992800	Enhancers	Stomach Mucosa	stomach
34	chr1:45990600-45992800	Enhancers	HepG2	liver
35	chr1:45990800-45991000	Enhancers	A549	lung
36	chr1:45990800-45991200	Enhancers	H1 Cell Line	embryonic stem cell
37	chr1:45990800-45991200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
38	chr1:45990800-45991400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin

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