Variant report

Variant	rs10918972
Chromosome Location	chr1:168721577-168721578
allele	C/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	ZNF217	chr1:168721223-168721827	MCF-7	breast:	n/a	n/a
2	GATA3	chr1:168721263-168721806	T-47D	breast:	n/a	chr1:168721635-168721642 chr1:168721631-168721647 chr1:168721628-168721649 chr1:168721635-168721644 chr1:168721634-168721644
3	SP1	chr1:168721125-168721957	A549	lung:	n/a	chr1:168721792-168721804 chr1:168721793-168721807 chr1:168721792-168721804 chr1:168721794-168721803
4	JUND	chr1:168721317-168721846	MCF-7	breast:	n/a	chr1:168721502-168721511 chr1:168721502-168721512 chr1:168721501-168721512 chr1:168721503-168721512 chr1:168721503-168721510
5	ATF3	chr1:168721269-168721743	A549	lung:	n/a	n/a
6	GABPA	chr1:168721277-168721787	A549	lung:	n/a	n/a
7	EP300	chr1:168721289-168721759	T-47D	breast:	n/a	chr1:168721628-168721637 chr1:168721503-168721512
8	TCF12	chr1:168721287-168721753	A549	lung:	n/a	n/a
9	GATA3	chr1:168721170-168721876	A549	lung:	n/a	chr1:168721635-168721642 chr1:168721631-168721647 chr1:168721628-168721649 chr1:168721635-168721644 chr1:168721634-168721644
10	JUND	chr1:168721339-168721634	HepG2	liver:	n/a	chr1:168721502-168721511 chr1:168721502-168721512 chr1:168721501-168721512 chr1:168721503-168721512 chr1:168721503-168721510
11	HDAC2	chr1:168721262-168721816	MCF-7	breast:	n/a	chr1:168721634-168721643
12	EP300	chr1:168721279-168721836	HepG2	liver:	n/a	chr1:168721628-168721637 chr1:168721503-168721512
13	FOS	chr1:168721373-168721596	MCF10A-Er-Src	breast:	n/a	chr1:168721502-168721511 chr1:168721502-168721512 chr1:168721503-168721512 chr1:168721503-168721510
14	CEBPB	chr1:168721185-168721901	A549	lung:	n/a	chr1:168721347-168721358 chr1:168721347-168721358
15	BCL3	chr1:168721159-168721804	A549	lung:	n/a	n/a
16	MAX	chr1:168721353-168722006	Hela-S3	cervix:	n/a	chr1:168721793-168721803
17	CEBPB	chr1:168721164-168721867	Hela-S3	cervix:	n/a	chr1:168721347-168721358 chr1:168721347-168721358
18	BRCA1	chr1:168721320-168721745	Hela-S3	cervix:	n/a	n/a
19	ZKSCAN1	chr1:168721533-168721735	Hela-S3	cervix:	n/a	n/a
20	SMC3	chr1:168721253-168721918	Hela-S3	cervix:	n/a	n/a
21	RFX5	chr1:168721435-168721861	Hela-S3	cervix:	n/a	n/a
22	RAD21	chr1:168721271-168721786	A549	lung:	n/a	n/a
23	MYC	chr1:168721382-168721876	Hela-S3	cervix:	n/a	chr1:168721793-168721803
24	MAX	chr1:168721227-168721812	A549	lung:	n/a	chr1:168721793-168721803
25	ELK1	chr1:168721478-168721740	Hela-S3	cervix:	n/a	n/a
26	JUND	chr1:168721194-168721722	T-47D	breast:	n/a	chr1:168721502-168721511 chr1:168721502-168721512 chr1:168721501-168721512 chr1:168721503-168721512 chr1:168721503-168721510
27	RAD21	chr1:168721268-168721804	A549	lung:	n/a	n/a
28	CEBPB	chr1:168721208-168721879	MCF-7	breast:	n/a	chr1:168721347-168721358 chr1:168721347-168721358
29	KAP1	chr1:168720220-168721969	U2OS	brain:	n/a	chr1:168721501-168721510
30	FOXM1	chr1:168721074-168721840	MCF-7	breast:	n/a	n/a
31	FOXA1	chr1:168721261-168721650	T-47D	breast:	n/a	n/a
32	SIN3AK20	chr1:168721140-168721902	MCF-7	breast:	n/a	n/a
33	FOSL2	chr1:168721249-168721740	A549	lung:	n/a	chr1:168721502-168721511 chr1:168721502-168721512 chr1:168721503-168721512 chr1:168721503-168721510
34	MAZ	chr1:168721202-168721772	Hela-S3	cervix:	n/a	n/a
35	CEBPB	chr1:168721165-168721881	MCF-7	breast:	n/a	chr1:168721347-168721358 chr1:168721347-168721358
36	JUND	chr1:168721287-168721791	A549	lung:	n/a	chr1:168721502-168721511 chr1:168721502-168721512 chr1:168721501-168721512 chr1:168721503-168721512 chr1:168721503-168721510
37	SP1	chr1:168721099-168722131	A549	lung:	n/a	chr1:168721792-168721804 chr1:168721793-168721807 chr1:168721792-168721804 chr1:168721794-168721803
38	FOS	chr1:168721338-168721584	MCF10A-Er-Src	breast:	n/a	chr1:168721502-168721511 chr1:168721502-168721512 chr1:168721503-168721512 chr1:168721503-168721510
39	RCOR1	chr1:168721340-168721791	Hela-S3	cervix:	n/a	n/a
40	FOXA2	chr1:168721239-168721995	A549	lung:	n/a	n/a
41	HDAC2	chr1:168721316-168721805	MCF-7	breast:	n/a	chr1:168721634-168721643
42	REST	chr1:168721238-168721906	A549	lung:	n/a	chr1:168721674-168721681
43	JUN	chr1:168721289-168721819	Hela-S3	cervix:	n/a	chr1:168721502-168721511 chr1:168721502-168721512 chr1:168721503-168721512 chr1:168721503-168721510
44	EP300	chr1:168721164-168721918	A549	lung:	n/a	chr1:168721628-168721637 chr1:168721503-168721512
45	MXI1	chr1:168721416-168721737	Hela-S3	cervix:	n/a	n/a
46	GATA3	chr1:168721233-168721898	MCF-7	breast:	n/a	chr1:168721635-168721642 chr1:168721631-168721647 chr1:168721628-168721649 chr1:168721635-168721644 chr1:168721634-168721644
47	RAD21	chr1:168721324-168721769	Hela-S3	cervix:	n/a	n/a
48	MAFK	chr1:168721287-168721700	Hela-S3	cervix:	n/a	chr1:168721623-168721638 chr1:168721501-168721510
49	FOS	chr1:168721346-168721661	MCF10A-Er-Src	breast:	n/a	chr1:168721502-168721511 chr1:168721502-168721512 chr1:168721503-168721512 chr1:168721503-168721510
50	FOSL2	chr1:168721072-168722013	A549	lung:	n/a	chr1:168721502-168721511 chr1:168721089-168721101 chr1:168721502-168721512 chr1:168721503-168721512 chr1:168721503-168721510

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:168717969..168723195-chr1:169075012..169079192,7	MCF-7	breast:

Variant related genes	Relation type
ENSG00000221578	TF binding region
ENSG00000143153	Chromatin interaction

Extended variants
information (count: 20 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:18)

rs_ID	r²[population]
rs10489362	0.84[ASN][1000 genomes]
rs10800378	0.97[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs10918970	0.81[EUR][1000 genomes]
rs12739280	0.84[ASN][1000 genomes]
rs2744666	0.96[AFR][1000 genomes]
rs2786758	0.85[ASN][1000 genomes]
rs2786759	0.97[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2786763	0.96[AFR][1000 genomes];0.84[ASN][1000 genomes]
rs2786764	0.85[ASN][1000 genomes]
rs35723976	0.85[ASN][1000 genomes]
rs485187	0.91[AFR][1000 genomes];0.81[AMR][1000 genomes];0.84[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs494189	0.91[AFR][1000 genomes];0.90[AMR][1000 genomes];0.86[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs552859	0.84[ASN][1000 genomes]
rs567067	0.83[AFR][1000 genomes];0.81[AMR][1000 genomes];0.83[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs628718	0.83[EUR][1000 genomes]
rs6427150	0.80[AMR][1000 genomes];0.97[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs6675239	0.81[AMR][1000 genomes];0.99[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs6690929	0.80[AMR][1000 genomes];0.97[EUR][1000 genomes];0.85[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv869415	chr1:168467284-169153863	Flanking Active TSS Weak transcription Enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh 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	44 gene(s)	inside rSNPs	diseases
2	nsv831847	chr1:168669877-168850129	Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:16 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:168711200-168724200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr1:168720000-168721600	Enhancers	Colon Smooth Muscle	Colon
3	chr1:168720000-168721600	Enhancers	Hela-S3	cervix
4	chr1:168720000-168722000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
5	chr1:168720200-168721800	Enhancers	Rectal Smooth Muscle	rectum
6	chr1:168720400-168722000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
7	chr1:168720600-168722200	Enhancers	Rectal Mucosa Donor 31	rectum
8	chr1:168720600-168722600	Enhancers	Fetal Lung	lung
9	chr1:168720800-168722000	Flanking Active TSS	A549	lung
10	chr1:168720800-168722000	Bivalent Enhancer	HepG2	liver
11	chr1:168720800-168724000	Weak transcription	Fetal Heart	heart
12	chr1:168721000-168723600	Weak transcription	Fetal Kidney	kidney
13	chr1:168721000-168723800	Weak transcription	Placenta Amnion	Placenta Amnion
14	chr1:168721200-168725400	Weak transcription	Pancreatic Islets	Pancreatic Islet
15	chr1:168721400-168722000	Enhancers	Stomach Mucosa	stomach
16	chr1:168721400-168725200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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