Variant report

Variant	rs10874021
Chromosome Location	chr1:79603940-79603941
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	SP1	chr1:79603722-79604335	A549	lung:	n/a	n/a
2	TCF12	chr1:79603826-79604326	A549	lung:	n/a	n/a
3	TEAD4	chr1:79603786-79604309	H1-hESC	embryonic stem cell:	n/a	n/a
4	CEBPB	chr1:79603920-79604175	H1-hESC	embryonic stem cell:	n/a	n/a
5	EP300	chr1:79603901-79604269	H1-hESC	embryonic stem cell:	n/a	n/a
6	USF1	chr1:79603919-79604325	H1-hESC	embryonic stem cell:	n/a	n/a
7	BCL11A	chr1:79603898-79604245	H1-hESC	embryonic stem cell:	n/a	n/a
8	TEAD4	chr1:79603836-79604314	H1-hESC	embryonic stem cell:	n/a	n/a
9	SP1	chr1:79603835-79604235	H1-hESC	embryonic stem cell:	n/a	n/a
10	REST	chr1:79603879-79604094	H1-hESC	embryonic stem cell:	n/a	n/a
11	EP300	chr1:79603830-79604324	A549	lung:	n/a	n/a
12	POLR2A	chr1:79603913-79604054	H1-hESC	embryonic stem cell:	n/a	n/a
13	ZNF143	chr1:79603909-79604186	H1-hESC	embryonic stem cell:	n/a	n/a
14	SP1	chr1:79603797-79604366	A549	lung:	n/a	n/a

Variant related genes	Relation type
ENSG00000266388	TF binding region

Extended variants
information (count: 37 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:30)

rs_ID	r²[population]
rs10735754	1.00[EUR][1000 genomes]
rs10874008	1.00[EUR][1000 genomes]
rs10874019	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11162602	1.00[EUR][1000 genomes]
rs11162639	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11162641	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12057337	1.00[EUR][1000 genomes]
rs1487543	1.00[EUR][1000 genomes]
rs1487558	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1487559	1.00[EUR][1000 genomes]
rs1953083	1.00[EUR][1000 genomes]
rs228456	1.00[AMR][1000 genomes]
rs228459	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs228464	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs228548	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs228555	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs402398	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4415519	1.00[EUR][1000 genomes]
rs4650385	1.00[EUR][1000 genomes]
rs4650386	1.00[EUR][1000 genomes]
rs4650637	1.00[EUR][1000 genomes]
rs61769016	1.00[EUR][1000 genomes]
rs6424629	1.00[EUR][1000 genomes]
rs6424635	1.00[EUR][1000 genomes]
rs6424636	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6662620	1.00[EUR][1000 genomes]
rs6684178	1.00[EUR][1000 genomes]
rs6700121	1.00[EUR][1000 genomes]
rs7527791	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7546780	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv491784	chr1:79146141-79853482	Enhancers Flanking Active TSS Active TSS Weak transcription Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
2	nsv546619	chr1:79233493-79614989	ZNF genes & repeats Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv546631	chr1:79518810-79614989	Enhancers Flanking Active TSS Active TSS Weak transcription ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	nsv1009913	chr1:79540957-79616947	Flanking Active TSS Enhancers Weak transcription Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
5	nsv1007013	chr1:79540957-79619725	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
6	nsv1005743	chr1:79540957-79621702	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
7	nsv830326	chr1:79573379-79735667	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:79595000-79604000	Weak transcription	A549	lung

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