Variant report

Variant	esv3421301
Chromosome Location	chr11:59435201-59437749
allele	n/a
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	ARID3A	chr11:59436573-59436852	K562	blood:	n/a	n/a
2	ARID3A	chr11:59436653-59437141	HepG2	liver:	n/a	n/a
3	ATF1	chr11:59436580-59437211	K562	blood:	n/a	n/a
4	ATF2	chr11:59436530-59436992	GM12878	blood:	n/a	n/a
5	ATF3	chr11:59436386-59437203	K562	blood:	n/a	n/a
6	BACH1	chr11:59436663-59437364	K562	blood:	n/a	n/a
7	BACH1	chr11:59435858-59437696	H1-hESC	embryonic stem cell:	n/a	n/a
8	BHLHE40	chr11:59436450-59437274	HepG2	liver:	n/a	n/a
9	BHLHE40	chr11:59436210-59437415	K562	blood:	n/a	n/a
10	BHLHE40	chr11:59435784-59435890	K562	blood:	n/a	n/a
11	BHLHE40	chr11:59436409-59437217	GM12878	blood:	n/a	n/a
12	BHLHE40	chr11:59436560-59437068	A549	lung:	n/a	n/a
13	BRCA1	chr11:59436688-59437056	HepG2	liver:	n/a	n/a
14	BRCA1	chr11:59435736-59436101	H1-hESC	embryonic stem cell:	n/a	n/a
15	BRCA1	chr11:59436572-59437559	Hela-S3	cervix:	n/a	chr11:59437315-59437322
16	BRCA1	chr11:59436604-59436912	GM12878	blood:	n/a	n/a
17	CBX3	chr11:59436425-59437381	K562	blood:	n/a	n/a
18	CBX3	chr11:59436830-59437110	K562	blood:	n/a	n/a
19	CCNT2	chr11:59436138-59437303	K562	blood:	n/a	n/a
20	CEBPB	chr11:59437114-59437691	ECC-1	luminal epithelium:	n/a	chr11:59437410-59437423 chr11:59437411-59437422
21	CEBPB	chr11:59436908-59437615	K562	blood:	n/a	chr11:59437410-59437423 chr11:59437411-59437422
22	CEBPB	chr11:59437139-59437657	A549	lung:	n/a	chr11:59437410-59437423 chr11:59437411-59437422
23	CEBPB	chr11:59435552-59435974	Hela-S3	cervix:	n/a	chr11:59435738-59435749 chr11:59435584-59435596
24	CEBPB	chr11:59436575-59437775	Hela-S3	cervix:	n/a	chr11:59437410-59437423 chr11:59437411-59437422
25	CEBPB	chr11:59435531-59435891	K562	blood:	n/a	chr11:59435738-59435749 chr11:59435584-59435596
26	CEBPB	chr11:59435560-59435931	IMR90	lung:	n/a	chr11:59435738-59435749 chr11:59435584-59435596
27	CEBPB	chr11:59435476-59436027	A549	lung:	n/a	chr11:59435738-59435749 chr11:59435584-59435596
28	CEBPB	chr11:59435561-59435914	K562	blood:	n/a	chr11:59435738-59435749 chr11:59435584-59435596
29	CEBPB	chr11:59435664-59435831	HepG2	liver:	n/a	chr11:59435738-59435749
30	CEBPB	chr11:59436969-59437680	K562	blood:	n/a	chr11:59437410-59437423 chr11:59437411-59437422
31	CEBPB	chr11:59437250-59437598	HepG2	liver:	n/a	chr11:59437410-59437423 chr11:59437411-59437422
32	CEBPB	chr11:59435588-59435896	H1-hESC	embryonic stem cell:	n/a	chr11:59435738-59435749
33	CEBPB	chr11:59435564-59435965	HepG2	liver:	n/a	chr11:59435738-59435749 chr11:59435584-59435596
34	CEBPB	chr11:59435604-59435943	A549	lung:	n/a	chr11:59435738-59435749
35	CEBPB	chr11:59437304-59437526	HepG2	liver:	n/a	chr11:59437410-59437423 chr11:59437411-59437422
36	CEBPB	chr11:59437226-59437604	HepG2	liver:	n/a	chr11:59437410-59437423 chr11:59437411-59437422
37	CEBPB	chr11:59435589-59435925	A549	lung:	n/a	chr11:59435738-59435749
38	CEBPB	chr11:59437013-59437715	A549	lung:	n/a	chr11:59437410-59437423 chr11:59437411-59437422
39	CEBPB	chr11:59437142-59437619	A549	lung:	n/a	chr11:59437410-59437423 chr11:59437411-59437422
40	CEBPB	chr11:59435400-59435928	HepG2	liver:	n/a	chr11:59435738-59435749 chr11:59435584-59435596
41	CEBPB	chr11:59437185-59437618	ECC-1	luminal epithelium:	n/a	chr11:59437410-59437423 chr11:59437411-59437422
42	CEBPB	chr11:59436753-59437650	IMR90	lung:	n/a	chr11:59437410-59437423 chr11:59437411-59437422
43	CEBPB	chr11:59436950-59437785	H1-hESC	embryonic stem cell:	n/a	chr11:59437410-59437423 chr11:59437411-59437422
44	CEBPB	chr11:59437148-59437605	MCF-7	breast:	n/a	chr11:59437410-59437423 chr11:59437411-59437422
45	CEBPB	chr11:59435602-59435948	MCF-7	breast:	n/a	chr11:59435738-59435749
46	CEBPB	chr11:59437156-59437643	MCF-7	breast:	n/a	chr11:59437410-59437423 chr11:59437411-59437422
47	CEBPB	chr11:59437190-59437542	K562	blood:	n/a	chr11:59437410-59437423 chr11:59437411-59437422
48	CEBPD	chr11:59436187-59436666	HepG2	liver:	n/a	n/a
49	CEBPD	chr11:59435650-59435909	HepG2	liver:	n/a	n/a
50	CHD1	chr11:59435822-59435871	H1-hESC	embryonic stem cell:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:59436646-59436696	Caco-2	colon:	n/a
2	chr11:59436769-59436819	GM12892	blood:	n/a
3	chr11:59436646-59436696	Caco-2	colon:	n/a
4	chr11:59436769-59436819	GM12892	blood:	n/a
5	chr11:59436238-59436288	T-47D	breast:	n/a
6	chr11:59435773-59435823	CMK	blood:	n/a
7	chr11:59437416-59437466	HEEpiC	esophagus:	n/a
8	chr11:59437344-59437394	A549	lung:	n/a
9	chr11:59436238-59436288	H1-hESC	embryonic stem cell:	embryo
10	chr11:59436746-59436796	HL-60	blood:	n/a
11	chr11:59437344-59437394	ovcar-3	ovarian:	n/a
12	chr11:59437344-59437394	GM19239	blood:	n/a
13	chr11:59436646-59436696	IMR90	lung:	fetal
14	chr11:59435997-59436047	ProgFib	skin:	n/a
15	chr11:59437416-59437466	HMEC	breast:	n/a
16	chr11:59436238-59436288	GM06990	blood:	n/a
17	chr11:59436746-59436796	AG10803	skin:	n/a
18	chr11:59436644-59436694	HEK293	kidney:	embryo
19	chr11:59436646-59436696	HepG2	liver:	n/a
20	chr11:59436646-59436696	Hepatocyte	liver:	n/a
21	chr11:59437344-59437394	HMEC	breast:	n/a
22	chr11:59435407-59435457	LNCaP	prostate:	n/a
23	chr11:59435997-59436047	LNCaP	prostate:	n/a
24	chr11:59436644-59436694	A549	lung:	n/a
25	chr11:59437416-59437466	HCPEpiC	choroid plexus:	n/a
26	chr11:59436746-59436796	SAEC	small airway:	n/a
27	chr11:59437416-59437466	AG04450	lung:	fetal
28	chr11:59436646-59436696	HAEpiC	amniotic membrane:	n/a
29	chr11:59435773-59435823	GM12892	blood:	n/a
30	chr11:59436646-59436696	HNPCEpiC	eye:	n/a
31	chr11:59436238-59436288	ovcar-3	ovarian:	n/a
32	chr11:59436746-59436796	MCF10A-Er-Src	breast:	n/a
33	chr11:59436769-59436819	GM06990	blood:	n/a
34	chr11:59435773-59435823	NT2-D1	testis:	n/a
35	chr11:59437231-59437281	T-47D	breast:	n/a
36	chr11:59435773-59435823	LNCaP	prostate:	n/a
37	chr11:59437231-59437281	H1-hESC	embryonic stem cell:	embryo
38	chr11:59436238-59436288	GM12891	blood:	n/a
39	chr11:59437344-59437394	HCPEpiC	choroid plexus:	n/a
40	chr11:59437344-59437394	BE2_C	brain:	n/a
41	chr11:59436646-59436696	SAEC	small airway:	n/a
42	chr11:59436769-59436819	ECC-1	luminal epithelium:	n/a
43	chr11:59436644-59436694	BE2_C	brain:	n/a
44	chr11:59436769-59436819	MCF10A-Er-Src	breast:	n/a
45	chr11:59435997-59436047	IMR90	lung:	fetal
46	chr11:59436238-59436288	PFSK-1	brain:	n/a
47	chr11:59435773-59435823	NB4	blood:	n/a
48	chr11:59437231-59437281	IMR90	lung:	fetal
49	chr11:59436238-59436288	AoSMC	blood vessel:	n/a
50	chr11:59436644-59436694	MCF10A-Er-Src	breast:	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:59435853..59436487-chr16:88729728..88730305,2	Hela-S3	cervix:
2	chr11:59435855..59436853-chr11:59577486..59578454,2	Hela-S3	cervix:
3	chr11:59331158..59335239-chr11:59432687..59436578,5	K562	blood:
4	chr11:59427010..59429204-chr11:59432808..59435498,2	MCF-7	breast:
5	chr11:59435931..59436776-chr15:43802144..43802835,2	NB4	blood:
6	chr1:152020083..152020779-chr11:59436443..59437077,2	NB4	blood:
7	chr11:59436476..59437342-chr8:23082198..23082970,2	Hela-S3	cervix:
8	chr11:59435921..59436657-chr14:24740330..24740936,2	Hela-S3	cervix:
9	chr11:59436531..59437288-chr14:20811174..20811933,2	Hela-S3	cervix:
10	chr11:59436077..59436715-chr3:100428082..100428818,2	Hela-S3	cervix:
11	chr11:59436513..59437364-chr5:132165817..132166567,2	Hela-S3	cervix:
12	chr11:59381143..59385193-chr11:59434975..59438411,10	K562	blood:
13	chr11:59379597..59385439-chr11:59434812..59438230,12	K562	blood:
14	chr11:59436447..59437072-chr2:242255223..242255824,2	Hela-S3	cervix:
15	chr11:59436284..59437132-chr18:12883857..12884750,2	Hela-S3	cervix:
16	chr11:59331158..59335239-chr11:59433739..59436205,3	K562	blood:
17	chr11:59436881..59439475-chr17:40074254..40076728,2	MCF-7	breast:
18	chr11:59436132..59436823-chr11:59522370..59523215,2	Hela-S3	cervix:
19	chr11:59380013..59385486-chr11:59434648..59438262,9	MCF-7	breast:
20	chr11:59436292..59437100-chr19:39936247..39937025,2	Hela-S3	cervix:
21	chr11:59436339..59437316-chr3:14165785..14166599,2	Hela-S3	cervix:
22	chr11:59436547..59437474-chr19:3572861..3573743,2	Hela-S3	cervix:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-STX3-1	chr11:59436785-59437015	ENSG00000255355.1

Variant related genes	Relation type
ENSG00000255355	TF binding region
PATL1	TF binding region
ENSG00000255355	CpG island
PATL1	CpG island
ENSG00000100949	chromatin interactions
ENSG00000163191	chromatin interactions
ENSG00000259001	chromatin interactions
ENSG00000255008	chromatin interactions
ENSG00000161091	chromatin interactions
ENSG00000175354	chromatin interactions
ENSG00000166902	chromatin interactions
ENSG00000246582	chromatin interactions
ENSG00000067369	chromatin interactions
ENSG00000114354	chromatin interactions
ENSG00000255139	chromatin interactions
ENSG00000166900	chromatin interactions
ENSG00000064961	chromatin interactions
ENSG00000115677	chromatin interactions
ENSG00000163528	chromatin interactions
ENSG00000170876	chromatin interactions
ENSG00000131473	chromatin interactions
ENSG00000168385	chromatin interactions
ENSG00000110048	chromatin interactions
ENSG00000260630	chromatin interactions
ENSG00000164403	chromatin interactions
ENSG00000104689	chromatin interactions
ENSG00000254477	chromatin interactions
ENSG00000129484	chromatin interactions
ENSG00000196235	chromatin interactions

Extended variants
information (count: 97 )
Associated
traits (count: 53 )

Variant overlapped rSNPs/rCNVs (count:97 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs532429843	chr11:59435235-59435236	Active TSS Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
2	rs545813108	chr11:59435241-59435242	Active TSS Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs562483197	chr11:59435347-59435348	Active TSS Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs559214431	chr11:59435392-59435393	Active TSS Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs529972006	chr11:59435394-59435395	Active TSS Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs183383365	chr11:59435408-59435409	Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs372344876	chr11:59435418-59435419	Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs373235440	chr11:59435430-59435431	Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs117285718	chr11:59435470-59435471	Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs536863041	chr11:59435478-59435479	Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs552202983	chr11:59435510-59435511	Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs369352693	chr11:59435529-59435530	Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs570498072	chr11:59435590-59435591	Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs534599033	chr11:59435628-59435629	Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs188839940	chr11:59435653-59435654	Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs373734738	chr11:59435684-59435685	Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs376799007	chr11:59435687-59435688	Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs572754059	chr11:59435726-59435727	Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs548235028	chr11:59435751-59435752	Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs536919829	chr11:59435755-59435756	Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs114626450	chr11:59435768-59435769	Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs376383264	chr11:59435774-59435775	Active TSS Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs193003668	chr11:59435785-59435786	Active TSS Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs80117447	chr11:59435817-59435818	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs183396083	chr11:59435864-59435865	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
26	rs541012062	chr11:59435907-59435908	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
27	rs75503950	chr11:59435918-59435919	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
28	rs72927435	chr11:59435951-59435952	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
29	rs186643042	chr11:59435952-59435953	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
30	rs548040151	chr11:59435971-59435972	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
31	rs563437834	chr11:59435979-59435980	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
32	rs530729550	chr11:59436029-59436030	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
33	rs552124406	chr11:59436063-59436064	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
34	rs564862830	chr11:59436065-59436066	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
35	rs371114490	chr11:59436087-59436088	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
36	rs534735214	chr11:59436102-59436103	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
37	rs546741780	chr11:59436165-59436166	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
38	rs150370443	chr11:59436207-59436208	Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
39	rs373046196	chr11:59436220-59436221	Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
40	rs535454537	chr11:59436238-59436239	Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
41	rs111432802	chr11:59436256-59436257	Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
42	rs555257391	chr11:59436278-59436279	Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
43	rs576710652	chr11:59436462-59436463	Active TSS	TF binding region Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
44	rs537642967	chr11:59436464-59436465	Active TSS	TF binding region Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
45	rs191523821	chr11:59436467-59436468	Active TSS	TF binding region Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
46	rs558921443	chr11:59436487-59436488	Active TSS	TF binding region Chromatin interactive region	21 gene(s)	Overlapped CNVs	n/a
47	rs532018108	chr11:59436489-59436490	Active TSS	TF binding region Chromatin interactive region	20 gene(s)	Overlapped CNVs	n/a
48	rs577248411	chr11:59436543-59436544	Active TSS	TF binding region Chromatin interactive region	23 gene(s)	Overlapped CNVs	n/a
49	rs541091599	chr11:59436544-59436545	Active TSS	TF binding region Chromatin interactive region	23 gene(s)	Overlapped CNVs	n/a
50	rs113037768	chr11:59436608-59436609	Active TSS	TF binding region Chromatin interactive region	24 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:53)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Wilms tumour	21544195	CNVD
Autism	22495311	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Glioblastoma multiforme	21138945	CNVD
Esophageal cancer	21851588	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Glioblastoma multiforme	22286061	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	21637783	CNVD
Acute myeloid leukemia	16864856	CNVD
Chronic lymphocytic leukemia	21795749	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21484798	CNVD
Ewing''s sarcoma	21437220	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	20837533	CNVD
Breast cancer	21264507	CNVD
Cervical cancer	21063398	CNVD
Glioblastoma multiforme	19960244	CNVD
Liposarcoma	21253554	CNVD
Neuroblastoma	18923524	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Neuroblastoma	17533364	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Colorectal cancer	16272173	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Pituitary adenoma	18645599	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Prostate cancer	18632612	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Smith-Lemli-Opitz syndrome	21572526	CNVD
Multiple myeloma	16461302	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Autism	22495309	CNVD
Autism	20808228	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:427 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:59409200-59435400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr11:59415400-59435400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
3	chr11:59425600-59435600	Weak transcription	Aorta	Aorta
4	chr11:59425600-59435600	Weak transcription	Gastric	stomach
5	chr11:59425800-59435400	Weak transcription	Pancreas	Pancrea
6	chr11:59426200-59435400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr11:59426200-59435400	Weak transcription	Esophagus	oesophagus
8	chr11:59427000-59435400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
9	chr11:59431800-59435400	Weak transcription	Placenta Amnion	Placenta Amnion
10	chr11:59433200-59435400	Weak transcription	Ovary	ovary
11	chr11:59433600-59435400	Weak transcription	Lung	lung
12	chr11:59433600-59435400	Weak transcription	Thymus	Thymus
13	chr11:59433600-59435400	Weak transcription	Spleen	Spleen
14	chr11:59433800-59435600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr11:59434200-59435400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr11:59434200-59435400	Weak transcription	Fetal Muscle Trunk	muscle
17	chr11:59434200-59435400	Weak transcription	Fetal Thymus	thymus
18	chr11:59434400-59435400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
19	chr11:59434400-59435400	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
20	chr11:59434400-59435400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
21	chr11:59434400-59435400	Enhancers	Brain Hippocampus Middle	brain
22	chr11:59434400-59435400	Weak transcription	Placenta	Placenta
23	chr11:59434400-59435400	Transcr. at gene 5' and 3'	Dnd41	blood
24	chr11:59434400-59435400	Active TSS	HSMMtube	muscle
25	chr11:59434400-59435400	Flanking Active TSS	NHDF-Ad	bronchial
26	chr11:59434400-59435600	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
27	chr11:59434400-59435600	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
28	chr11:59434400-59435600	Flanking Active TSS	Liver	Liver
29	chr11:59434400-59436000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
30	chr11:59434400-59437400	Active TSS	NHLF	lung
31	chr11:59434600-59435400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
32	chr11:59434600-59435400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
33	chr11:59434600-59435400	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
34	chr11:59434600-59435400	Weak transcription	Primary T cells fromperipheralblood	blood
35	chr11:59434600-59435400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
36	chr11:59434600-59435400	Enhancers	Primary T helper cells fromperipheralblood	blood
37	chr11:59434600-59435400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
38	chr11:59434600-59435400	Enhancers	Brain Angular Gyrus	brain
39	chr11:59434600-59435400	Enhancers	Brain Cingulate Gyrus	brain
40	chr11:59434600-59435400	Enhancers	Stomach Mucosa	stomach
41	chr11:59434600-59435800	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
42	chr11:59434600-59435800	Flanking Active TSS	NHEK	skin
43	chr11:59434600-59435800	Flanking Active TSS	Osteobl	bone
44	chr11:59434600-59436000	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
45	chr11:59434600-59436000	Flanking Active TSS	Primary hematopoietic stem cells	blood
46	chr11:59434600-59436000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
47	chr11:59434600-59436000	Flanking Active TSS	Adipose Nuclei	Adipose
48	chr11:59434600-59438400	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
49	chr11:59434800-59435400	Enhancers	Brain Anterior Caudate	brain
50	chr11:59434800-59435600	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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