Variant report

Variant	rs149239786
Chromosome Location	chr11:67769604-67769605
allele	A/G
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	MYC	chr11:67769508-67769870	HepG2	liver:	n/a	chr11:67769702-67769713 chr11:67769699-67769714
2	ZNF384	chr11:67769525-67769777	K562	blood:	n/a	n/a
3	MAX	chr11:67769560-67769803	GM12878	blood:	n/a	chr11:67769702-67769713 chr11:67769699-67769714
4	MYBL2	chr11:67769451-67769782	HepG2	liver:	n/a	n/a
5	MYC	chr11:67769603-67769769	MCF-7	breast:	n/a	chr11:67769702-67769713 chr11:67769699-67769714
6	ZNF384	chr11:67769435-67769806	GM12878	blood:	n/a	n/a
7	MYC	chr11:67769573-67769833	K562	blood:	n/a	chr11:67769702-67769713 chr11:67769699-67769714
8	FOXA1	chr11:67769468-67769798	HepG2	liver:	n/a	n/a
9	JUND	chr11:67769557-67769786	HepG2	liver:	n/a	n/a
10	FOXA1	chr11:67769374-67769822	HepG2	liver:	n/a	n/a
11	POLR2A	chr11:67769379-67769763	HepG2	liver:	n/a	n/a
12	MAX	chr11:67769401-67769976	HepG2	liver:	n/a	chr11:67769702-67769713 chr11:67769699-67769714
13	MXI1	chr11:67769536-67769877	HepG2	liver:	n/a	n/a
14	FOXA2	chr11:67769483-67769790	HepG2	liver:	n/a	n/a
15	MAX	chr11:67769439-67769917	HepG2	liver:	n/a	chr11:67769702-67769713 chr11:67769699-67769714
16	BHLHE40	chr11:67769526-67770501	GM12878	blood:	n/a	n/a
17	BHLHE40	chr11:67769551-67769812	K562	blood:	n/a	n/a
18	POLR2A	chr11:67769173-67769768	GM12878	blood:	n/a	n/a
19	POLR2A	chr11:67769490-67769776	GM12878	blood:	n/a	n/a
20	SP1	chr11:67769446-67769875	HepG2	liver:	n/a	n/a
21	MYC	chr11:67769557-67769805	MCF-7	breast:	n/a	chr11:67769702-67769713 chr11:67769699-67769714
22	MAX	chr11:67769547-67769830	HepG2	liver:	n/a	chr11:67769702-67769713 chr11:67769699-67769714
23	EP300	chr11:67769482-67769877	HepG2	liver:	n/a	n/a
24	POLR2A	chr11:67769585-67769791	GM12878	blood:	n/a	n/a
25	MAX	chr11:67769526-67769800	K562	blood:	n/a	chr11:67769702-67769713 chr11:67769699-67769714
26	HDAC2	chr11:67769496-67769825	HepG2	liver:	n/a	n/a
27	MYC	chr11:67769573-67769784	GM12878	blood:	n/a	chr11:67769702-67769713 chr11:67769699-67769714
28	BHLHE40	chr11:67769596-67769806	HepG2	liver:	n/a	n/a
29	BHLHE40	chr11:67769512-67769893	HepG2	liver:	n/a	n/a
30	MAZ	chr11:67769604-67769786	HepG2	liver:	n/a	chr11:67769702-67769713 chr11:67769699-67769714
31	FOXA2	chr11:67769317-67769828	A549	lung:	n/a	n/a
32	MAX	chr11:67769445-67769902	MCF-7	breast:	n/a	chr11:67769702-67769713 chr11:67769699-67769714
33	POLR2A	chr11:67769503-67771310	HL-60	blood:	n/a	n/a
34	MAX	chr11:67769575-67769822	K562	blood:	n/a	chr11:67769702-67769713 chr11:67769699-67769714
35	FOXA2	chr11:67769427-67769892	HepG2	liver:	n/a	n/a
36	FOXA1	chr11:67769459-67769901	HepG2	liver:	n/a	n/a
37	FOXA1	chr11:67769469-67769770	HepG2	liver:	n/a	n/a
38	USF1	chr11:67769559-67769776	HepG2	liver:	n/a	n/a
39	SIN3AK20	chr11:67769586-67769745	HepG2	liver:	n/a	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr11:67763621..67766711-chr11:67769461..67772575,7	MCF-7	breast:
2	chr11:67762605..67767485-chr11:67767779..67773135,10	K562	blood:

Variant related genes	Relation type
UNC93B1	TF binding region
ENSG00000110057	Chromatin interaction

Extended variants
information (count: 34 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:34 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1036101	chr11:67346813-67828351	Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Active TSS Weak transcription Genic enhancers Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	139 gene(s)	inside rSNPs	diseases
2	nsv541079	chr11:67346813-67828351	Enhancers Flanking Active TSS Active TSS Weak transcription Strong transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	139 gene(s)	inside rSNPs	diseases
3	nsv468606	chr11:67352689-67816936	Active TSS Flanking Bivalent TSS/Enh Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	136 gene(s)	inside rSNPs	diseases
4	nsv555269	chr11:67352689-67816936	Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Strong transcription Genic enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	136 gene(s)	inside rSNPs	diseases
5	nsv427892	chr11:67451649-67926562	Bivalent Enhancer Weak transcription Strong transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	116 gene(s)	inside rSNPs	diseases
6	esv2757450	chr11:67472905-67891289	Enhancers Flanking Active TSS Weak transcription Active TSS Strong transcription Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	112 gene(s)	inside rSNPs	diseases
7	esv2759835	chr11:67472905-67891289	Strong transcription Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	112 gene(s)	inside rSNPs	diseases
8	nsv428260	chr11:67524937-67797669	Enhancers Active TSS Bivalent Enhancer Weak transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	80 gene(s)	inside rSNPs	diseases
9	esv2758275	chr11:67524937-67859490	Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	87 gene(s)	inside rSNPs	diseases
10	nsv469856	chr11:67639037-67859490	Weak transcription Active TSS Strong transcription Enhancers Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	73 gene(s)	inside rSNPs	diseases
11	nsv482760	chr11:67639037-67859490	Strong transcription Active TSS Enhancers Genic enhancers Flanking Active TSS ZNF genes & repeats Weak transcription Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	73 gene(s)	inside rSNPs	diseases
12	nsv1038960	chr11:67727827-67785555	Bivalent Enhancer Strong transcription Enhancers Flanking Active TSS Weak transcription Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	55 gene(s)	inside rSNPs	diseases
13	nsv1047567	chr11:67747160-67819790	Flanking Active TSS Enhancers Active TSS Genic enhancers Strong transcription Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	62 gene(s)	inside rSNPs	diseases
14	nsv8836	chr11:67752879-67819799	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	61 gene(s)	inside rSNPs	diseases
15	nsv983037	chr11:67756642-67778389	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent/Poised TSS Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	43 gene(s)	inside rSNPs	diseases
16	nsv897836	chr11:67757350-67816936	Enhancers Flanking Active TSS Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	61 gene(s)	inside rSNPs	diseases
17	nsv897837	chr11:67757350-67821036	Genic enhancers Enhancers Flanking Active TSS Weak transcription Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	61 gene(s)	inside rSNPs	diseases
18	nsv897838	chr11:67757350-67833543	Active TSS Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	61 gene(s)	inside rSNPs	diseases
19	nsv482160	chr11:67758575-67771593	Active TSS Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers Flanking Active TSS Strong transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	11 gene(s)	inside rSNPs	diseases
20	nsv825963	chr11:67763676-68197054	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	149 gene(s)	inside rSNPs	diseases
21	nsv1050471	chr11:67764068-67821610	Weak transcription Strong transcription Enhancers Genic enhancers Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	61 gene(s)	inside rSNPs	diseases
22	nsv897839	chr11:67765056-67793014	Genic enhancers Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Active TSS Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	53 gene(s)	inside rSNPs	diseases
23	nsv468613	chr11:67765056-67794643	Weak transcription Active TSS Enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	53 gene(s)	inside rSNPs	diseases
24	nsv555277	chr11:67765056-67794643	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	53 gene(s)	inside rSNPs	diseases
25	nsv468614	chr11:67765056-67799926	ZNF genes & repeats Active TSS Enhancers Weak transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	57 gene(s)	inside rSNPs	diseases
26	nsv897840	chr11:67765056-67804605	Weak transcription Strong transcription Genic enhancers Flanking Active TSS Enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	58 gene(s)	inside rSNPs	diseases
27	nsv468615	chr11:67765056-67816936	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	61 gene(s)	inside rSNPs	diseases
28	nsv555278	chr11:67765056-67816936	Enhancers Genic enhancers Bivalent/Poised TSS Flanking Active TSS Weak transcription Active TSS Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	61 gene(s)	inside rSNPs	diseases
29	nsv897841	chr11:67765056-67816936	Bivalent Enhancer Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	61 gene(s)	inside rSNPs	diseases
30	nsv469964	chr11:67765056-67821036	Active TSS Flanking Active TSS Weak transcription Strong transcription Bivalent/Poised TSS Enhancers Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	61 gene(s)	inside rSNPs	diseases
31	nsv897842	chr11:67765056-67821036	Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	61 gene(s)	inside rSNPs	diseases
32	nsv897843	chr11:67765056-67833543	Flanking Active TSS Weak transcription Active TSS Strong transcription Enhancers Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	61 gene(s)	inside rSNPs	diseases
33	nsv1046054	chr11:67768796-67819790	Weak transcription Strong transcription Flanking Active TSS Enhancers ZNF genes & repeats Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	60 gene(s)	inside rSNPs	diseases
34	esv3372157	chr11:67769401-67772749	Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region	10 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:79 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:67759200-67770400	Weak transcription	Placenta Amnion	Placenta Amnion
2	chr11:67759200-67770400	Weak transcription	Right Atrium	heart
3	chr11:67761400-67769800	Genic enhancers	Primary B cells from peripheral blood	blood
4	chr11:67762000-67770400	Weak transcription	NHLF	lung
5	chr11:67763600-67769800	Genic enhancers	Primary monocytes fromperipheralblood	blood
6	chr11:67763800-67770400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
7	chr11:67764200-67770000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
8	chr11:67764400-67770600	Weak transcription	Small Intestine	intestine
9	chr11:67764600-67770000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
10	chr11:67764600-67770000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
11	chr11:67764600-67770000	Weak transcription	Fetal Muscle Leg	muscle
12	chr11:67764600-67770600	Weak transcription	Right Ventricle	heart
13	chr11:67764800-67769800	Weak transcription	Adipose Nuclei	Adipose
14	chr11:67764800-67770200	Weak transcription	Esophagus	oesophagus
15	chr11:67764800-67770400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
16	chr11:67765000-67770000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
17	chr11:67765000-67770000	Weak transcription	Stomach Mucosa	stomach
18	chr11:67765000-67770200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
19	chr11:67765000-67770400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
20	chr11:67765000-67770400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
21	chr11:67765000-67770800	Weak transcription	K562	blood
22	chr11:67765200-67769800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
23	chr11:67765200-67770000	Weak transcription	Placenta	Placenta
24	chr11:67765200-67770000	Weak transcription	Pancreas	Pancrea
25	chr11:67765200-67770400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
26	chr11:67765400-67769800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
27	chr11:67765400-67769800	Weak transcription	Hela-S3	cervix
28	chr11:67765400-67770000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
29	chr11:67765400-67770000	Weak transcription	Colonic Mucosa	Colon
30	chr11:67765400-67770200	Weak transcription	H1 Cell Line	embryonic stem cell
31	chr11:67765600-67770200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
32	chr11:67765600-67770400	Weak transcription	Sigmoid Colon	Sigmoid Colon
33	chr11:67765800-67770000	Weak transcription	Rectal Mucosa Donor 31	rectum
34	chr11:67766000-67770000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
35	chr11:67766000-67770600	Weak transcription	Primary T cells from cord blood	blood
36	chr11:67766200-67769800	Weak transcription	Primary T helper cells PMA-I stimulated	--
37	chr11:67766200-67769800	Weak transcription	Rectal Mucosa Donor 29	rectum
38	chr11:67766200-67770000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
39	chr11:67766200-67770400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
40	chr11:67766200-67771400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
41	chr11:67766400-67770000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr11:67766400-67770800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
43	chr11:67766400-67770800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
44	chr11:67766600-67769800	Weak transcription	Primary hematopoietic stem cells	blood
45	chr11:67766600-67769800	Weak transcription	Primary T helper cells fromperipheralblood	blood
46	chr11:67766600-67770000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
47	chr11:67767000-67769800	Weak transcription	Duodenum Mucosa	Duodenum
48	chr11:67767200-67769800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
49	chr11:67767200-67770000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
50	chr11:67767400-67770000	Weak transcription	Primary T cells fromperipheralblood	blood

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