Variant report

Variant	rs7514679
Chromosome Location	chr1:92414472-92414473
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	CEBPB	chr1:92414360-92414677	A549	lung:	n/a	n/a
2	CEBPB	chr1:92414387-92414664	A549	lung:	n/a	n/a
3	CEBPB	chr1:92414333-92414714	K562	blood:	n/a	n/a
4	CEBPB	chr1:92414365-92414690	H1-hESC	embryonic stem cell:	n/a	n/a
5	CEBPB	chr1:92414340-92414704	IMR90	lung:	n/a	n/a
6	CEBPB	chr1:92414325-92414702	K562	blood:	n/a	n/a
7	CEBPB	chr1:92414400-92414603	MCF-7	breast:	n/a	n/a
8	CEBPB	chr1:92414332-92414701	HepG2	liver:	n/a	n/a
9	CEBPB	chr1:92414369-92414701	A549	lung:	n/a	n/a

Variant related genes	Relation type
BRDT	TF binding region

Extended variants
information (count: 88 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:62)

rs_ID	r²[population]
rs11466552	1.00[ASN][1000 genomes]
rs11466555	1.00[ASN][1000 genomes]
rs12032808	1.00[ASN][1000 genomes]
rs17131587	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17131594	1.00[CHB][hapmap];1.00[GIH][hapmap];1.00[ASN][1000 genomes]
rs17131596	1.00[CHB][hapmap]
rs17886020	1.00[ASN][1000 genomes]
rs2799519	1.00[ASN][1000 genomes]
rs2799520	1.00[ASN][1000 genomes]
rs3862907	1.00[CHB][hapmap];1.00[GIH][hapmap];1.00[ASN][1000 genomes]
rs4367824	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs495446	1.00[CHB][hapmap]
rs525834	1.00[CHB][hapmap]
rs533418	1.00[CHB][hapmap]
rs541168	1.00[CHB][hapmap]
rs548100	1.00[CHB][hapmap]
rs553173	1.00[CHB][hapmap]
rs55813648	1.00[ASN][1000 genomes]
rs562119	1.00[CHB][hapmap]
rs564077	1.00[CHB][hapmap]
rs57053265	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs58094327	1.00[ASN][1000 genomes]
rs58281825	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59345962	1.00[ASN][1000 genomes]
rs60483196	1.00[ASN][1000 genomes]
rs60765274	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61053596	0.86[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs6604065	1.00[ASN][1000 genomes]
rs6604066	1.00[ASN][1000 genomes]
rs6604071	0.82[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs6656473	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6663157	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6664544	1.00[CHB][hapmap]
rs6668529	1.00[CHB][hapmap]
rs66687439	1.00[ASN][1000 genomes]
rs6696071	1.00[CHB][hapmap]
rs6696315	1.00[ASN][1000 genomes]
rs6699466	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6700124	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[GIH][hapmap];0.85[LWK][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6703718	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs67510747	1.00[ASN][1000 genomes]
rs67577913	1.00[ASN][1000 genomes]
rs72716472	1.00[ASN][1000 genomes]
rs72716484	1.00[ASN][1000 genomes]
rs74101025	1.00[ASN][1000 genomes]
rs74101047	0.85[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs74101048	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs74101069	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs74101079	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs74101080	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs74101081	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs74101089	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs74101097	1.00[ASN][1000 genomes]
rs7516778	1.00[ASN][1000 genomes]
rs7540938	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7541252	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7544958	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7545710	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs877277	1.00[ASN][1000 genomes]
rs883872	1.00[ASN][1000 genomes]
rs883873	1.00[ASN][1000 genomes]
rs9659484	1.00[CHB][hapmap]

Variant overlapped rSNPs/rCNVs (count:26 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1012864	chr1:92067100-92827761	Flanking Active TSS Strong transcription Enhancers Active TSS Weak transcription Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
2	nsv535029	chr1:92067100-92827761	Strong transcription Weak transcription Enhancers Active TSS Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
3	nsv530438	chr1:92091957-92827760	Weak transcription Active TSS Strong transcription Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
4	nsv1010179	chr1:92140209-92655952	Weak transcription Genic enhancers Flanking Active TSS Enhancers Strong transcription Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
5	nsv535030	chr1:92140209-92655952	Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
6	nsv949449	chr1:92211020-92585831	Strong transcription Enhancers Genic enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
7	nsv524845	chr1:92215725-92598705	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
8	nsv462517	chr1:92215725-92598705	Weak transcription Bivalent Enhancer Enhancers Active TSS Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
9	nsv546810	chr1:92215725-92598705	Flanking Active TSS Enhancers Weak transcription Active TSS Genic enhancers Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
10	nsv1006318	chr1:92216408-92608324	Flanking Active TSS Enhancers Active TSS Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
11	nsv432498	chr1:92218245-92618323	Weak transcription Strong transcription Genic enhancers Flanking Active TSS Enhancers Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
12	nsv1004570	chr1:92220544-92622129	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
13	nsv1007661	chr1:92220544-92655952	Weak transcription Enhancers Active TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
14	nsv1014837	chr1:92233905-92618839	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
15	nsv535031	chr1:92233905-92618839	Bivalent/Poised TSS Enhancers Weak transcription Bivalent Enhancer Genic enhancers Strong transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
16	nsv1012134	chr1:92235485-92598800	Weak transcription Genic enhancers Flanking Active TSS Active TSS Enhancers Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
17	nsv546818	chr1:92236048-92579206	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
18	nsv546819	chr1:92256626-92558583	Strong transcription Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
19	nsv546820	chr1:92273644-92558583	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
20	nsv530046	chr1:92277460-92799794	Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Weak transcription Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
21	nsv1007270	chr1:92289298-92598800	Active TSS Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Strong transcription Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
22	nsv1002730	chr1:92302541-92565229	Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
23	nsv830581	chr1:92317207-92511175	Enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription Flanking Active TSS Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
24	nsv871415	chr1:92340684-92641607	Weak transcription Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
25	esv2750842	chr1:92356781-92579675	Flanking Active TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
26	nsv871144	chr1:92380302-92641607	Enhancers Strong transcription Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:17 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:92413000-92415400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
2	chr1:92413600-92414600	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
3	chr1:92413600-92415000	Flanking Active TSS	Primary T cells fromperipheralblood	blood
4	chr1:92413600-92415000	Flanking Active TSS	Primary T helper memory cells from peripheral blood 2	blood
5	chr1:92413800-92414600	Enhancers	Primary T regulatory cells fromperipheralblood	blood
6	chr1:92413800-92414800	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
7	chr1:92413800-92414800	Flanking Active TSS	Primary Natural Killer cells fromperipheralblood	blood
8	chr1:92414000-92414600	Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
9	chr1:92414000-92414800	Enhancers	GM12878-XiMat	blood
10	chr1:92414000-92415000	Enhancers	Fetal Thymus	thymus
11	chr1:92414200-92414600	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
12	chr1:92414200-92414800	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
13	chr1:92414200-92414800	Flanking Active TSS	Primary T killer memory cells from peripheral blood	blood
14	chr1:92414400-92414600	Flanking Active TSS	Primary mononuclear cells fromperipheralblood	Blood
15	chr1:92414400-92414800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
16	chr1:92414400-92414800	Enhancers	Fetal Muscle Leg	muscle
17	chr1:92414400-92415400	Flanking Active TSS	Placenta	Placenta

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