Variant report

Variant	nsv896926
Chromosome Location	chr11:5143309-5170510
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:454)
CpG islands
(count:305)
Chromatin interactive
region (count:50)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:454 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:5151921-5153769	K562	blood:	n/a	n/a
2	ARID3A	chr11:5145337-5145816	K562	blood:	n/a	n/a
3	ARID3A	chr11:5150153-5151193	K562	blood:	n/a	n/a
4	ATF1	chr11:5153059-5153491	K562	blood:	n/a	n/a
5	ATF1	chr11:5150550-5151082	K562	blood:	n/a	n/a
6	ATF3	chr11:5150491-5151003	K562	blood:	n/a	n/a
7	BACH1	chr11:5153269-5154148	K562	blood:	n/a	n/a
8	BHLHE40	chr11:5152969-5153636	K562	blood:	n/a	n/a
9	BHLHE40	chr11:5145393-5145647	K562	blood:	n/a	n/a
10	BHLHE40	chr11:5145321-5145613	GM12878	blood:	n/a	n/a
11	CBX3	chr11:5152914-5153556	K562	blood:	n/a	n/a
12	CCNT2	chr11:5152975-5153809	K562	blood:	n/a	n/a
13	CCNT2	chr11:5150752-5151154	K562	blood:	n/a	n/a
14	CEBPB	chr11:5150229-5151243	K562	blood:	n/a	chr11:5150735-5150746
15	CEBPB	chr11:5145124-5145643	K562	blood:	n/a	chr11:5145432-5145443 chr11:5145432-5145445
16	CEBPB	chr11:5145344-5145671	A549	lung:	n/a	chr11:5145432-5145443 chr11:5145432-5145445
17	CEBPB	chr11:5167951-5168183	IMR90	lung:	n/a	chr11:5168038-5168049 chr11:5168039-5168050 chr11:5168038-5168051 chr11:5168040-5168049
18	CEBPB	chr11:5167046-5167192	K562	blood:	n/a	n/a
19	CEBPB	chr11:5145160-5145706	A549	lung:	n/a	chr11:5145432-5145443 chr11:5145432-5145445
20	CEBPB	chr11:5158926-5159114	HepG2	liver:	n/a	chr11:5158987-5158998
21	CEBPB	chr11:5145351-5145641	ECC-1	luminal epithelium:	n/a	chr11:5145432-5145443 chr11:5145432-5145445
22	CEBPB	chr11:5155439-5155486	K562	blood:	n/a	chr11:5155443-5155454 chr11:5155443-5155454
23	CEBPB	chr11:5150602-5150922	K562	blood:	n/a	chr11:5150735-5150746
24	CEBPB	chr11:5150548-5150936	IMR90	lung:	n/a	chr11:5150735-5150746
25	CEBPB	chr11:5145178-5145630	Hela-S3	cervix:	n/a	chr11:5145432-5145443 chr11:5145432-5145445
26	CEBPB	chr11:5145163-5145709	K562	blood:	n/a	chr11:5145432-5145443 chr11:5145432-5145445
27	CEBPB	chr11:5167900-5168180	HepG2	liver:	n/a	chr11:5168038-5168049 chr11:5168039-5168050 chr11:5168038-5168051 chr11:5168040-5168049
28	CEBPB	chr11:5152905-5153566	K562	blood:	n/a	n/a
29	CEBPB	chr11:5145211-5145624	H1-hESC	embryonic stem cell:	n/a	chr11:5145432-5145443 chr11:5145432-5145445
30	CEBPB	chr11:5145304-5145631	MCF-7	breast:	n/a	chr11:5145432-5145443 chr11:5145432-5145445
31	CEBPB	chr11:5150320-5151240	K562	blood:	n/a	chr11:5150735-5150746
32	CEBPB	chr11:5145225-5145631	A549	lung:	n/a	chr11:5145432-5145443 chr11:5145432-5145445
33	CEBPB	chr11:5145333-5145526	K562	blood:	n/a	chr11:5145432-5145443 chr11:5145432-5145445
34	CEBPB	chr11:5150573-5150918	A549	lung:	n/a	chr11:5150735-5150746
35	CEBPB	chr11:5152900-5153523	K562	blood:	n/a	n/a
36	CEBPB	chr11:5145260-5145622	HepG2	liver:	n/a	chr11:5145432-5145443 chr11:5145432-5145445
37	CEBPB	chr11:5145207-5145650	MCF-7	breast:	n/a	chr11:5145432-5145443 chr11:5145432-5145445
38	CEBPB	chr11:5150241-5150936	Hela-S3	cervix:	n/a	chr11:5150735-5150746
39	CEBPB	chr11:5150613-5150884	HepG2	liver:	n/a	chr11:5150735-5150746
40	CEBPB	chr11:5145168-5145641	IMR90	lung:	n/a	chr11:5145432-5145443 chr11:5145432-5145445
41	CEBPB	chr11:5147292-5147370	A549	lung:	n/a	n/a
42	CEBPB	chr11:5167910-5168140	K562	blood:	n/a	chr11:5168038-5168049 chr11:5168039-5168050 chr11:5168038-5168051 chr11:5168040-5168049
43	CEBPB	chr11:5145365-5145512	HepG2	liver:	n/a	chr11:5145432-5145443 chr11:5145432-5145445
44	CEBPD	chr11:5152959-5153581	K562	blood:	n/a	n/a
45	CEBPD	chr11:5150494-5151221	K562	blood:	n/a	n/a
46	CEBPD	chr11:5152911-5153517	K562	blood:	n/a	n/a
47	CEBPD	chr11:5150511-5151086	K562	blood:	n/a	n/a
48	CHD2	chr11:5153413-5153475	K562	blood:	n/a	n/a
49	CTCF	chr11:5145342-5145617	HUVEC	blood vessel:	n/a	chr11:5145472-5145493 chr11:5145473-5145486 chr11:5145470-5145488
50	CTCF	chr11:5150253-5150474	K562	blood:	n/a	n/a

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:5165693-5165743	HCPEpiC	choroid plexus:	n/a
2	chr11:5143555-5143605	Caco-2	colon:	n/a
3	chr11:5153834-5153884	GM12891	blood:	n/a
4	chr11:5153834-5153884	MCF-7	breast:	n/a
5	chr11:5143555-5143605	GM12891	blood:	n/a
6	chr11:5166758-5166808	GM12878	blood:	n/a
7	chr11:5165693-5165743	MCF-7	breast:	n/a
8	chr11:5144101-5144151	HPAEpiC	pulmonary alveolar:	n/a
9	chr11:5153834-5153884	Caco-2	colon:	n/a
10	chr11:5143555-5143605	SK-N-MC	brain:	n/a
11	chr11:5153834-5153884	HCPEpiC	choroid plexus:	n/a
12	chr11:5144101-5144151	HCF	heart:	n/a
13	chr11:5143555-5143605	NHBE	bronchial:	n/a
14	chr11:5153834-5153884	HRCEpiC	kidney:	n/a
15	chr11:5143555-5143605	SAEC	small airway:	n/a
16	chr11:5165693-5165743	HCM	heart:	n/a
17	chr11:5153834-5153884	AG10803	skin:	n/a
18	chr11:5166758-5166808	NH-A	brain:	n/a
19	chr11:5143555-5143605	AoSMC	blood vessel:	n/a
20	chr11:5165693-5165743	GM12892	blood:	n/a
21	chr11:5166758-5166808	HL-60	blood:	n/a
22	chr11:5166758-5166808	Hela-S3	cervix:	n/a
23	chr11:5144101-5144151	HCM	heart:	n/a
24	chr11:5165693-5165743	HepG2	liver:	n/a
25	chr11:5165693-5165743	Jurkat	blood:	n/a
26	chr11:5165693-5165743	BJ	skin:	n/a
27	chr11:5166758-5166808	HIPEpiC	eye:	n/a
28	chr11:5166758-5166808	IMR90	lung:	fetal
29	chr11:5166758-5166808	AG10803	skin:	n/a
30	chr11:5153834-5153884	LNCaP	prostate:	n/a
31	chr11:5144101-5144151	AG09319	gingival:	n/a
32	chr11:5153834-5153884	HCT-116	colon:	n/a
33	chr11:5165693-5165743	HRE	kidney:	n/a
34	chr11:5153834-5153884	HAEpiC	amniotic membrane:	n/a
35	chr11:5165693-5165743	A549	lung:	n/a
36	chr11:5165693-5165743	NHBE	bronchial:	n/a
37	chr11:5153834-5153884	GM12878	blood:	n/a
38	chr11:5143555-5143605	HCF	heart:	n/a
39	chr11:5143555-5143605	HRPEpiC	eye:	n/a
40	chr11:5153834-5153884	HEK293	kidney:	embryo
41	chr11:5153834-5153884	GM06990	blood:	n/a
42	chr11:5153834-5153884	GM12892	blood:	n/a
43	chr11:5144101-5144151	NT2-D1	testis:	n/a
44	chr11:5144101-5144151	Jurkat	blood:	n/a
45	chr11:5165693-5165743	T-47D	breast:	n/a
46	chr11:5165693-5165743	HRCEpiC	kidney:	n/a
47	chr11:5153834-5153884	PFSK-1	brain:	n/a
48	chr11:5166758-5166808	GM06990	blood:	n/a
49	chr11:5166758-5166808	RPTEC	kidney:	n/a
50	chr11:5166758-5166808	HRCEpiC	kidney:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr11:5140099..5148928-chr11:5149317..5155604,15	K562	blood:
2	chr11:5150699..5153690-chr11:5165729..5169449,3	K562	blood:
3	chr11:5149232..5151969-chr11:5305732..5307416,2	K562	blood:
4	chr11:5150801..5152523-chr11:5295728..5297239,2	K562	blood:
5	chr11:5150404..5153191-chr11:5303094..5304941,2	K562	blood:
6	chr11:5150718..5153704-chr11:5259366..5262458,3	K562	blood:
7	11:5154908-5159254..11:5721056-5732713	GM12878	blood:
8	chr11:5140099..5148928-chr11:5149317..5155604,15	K562	blood:
9	chr11:5145799..5146631-chr11:5217510..5218294,2	K562	blood:
10	chr11:5149697..5151826-chr11:5212442..5214718,2	K562	blood:
11	chr11:5149389..5153211-chr11:5272377..5275357,4	K562	blood:
12	chr11:5154058..5155935-chr11:5165888..5170423,4	K562	blood:
13	chr11:5167216..5169602-chr11:5170013..5172866,3	K562	blood:
14	chr11:5163553..5165336-chr11:5177083..5178802,2	K562	blood:
15	chr11:5154058..5155935-chr11:5165888..5170423,4	K562	blood:
16	chr11:5170489..5172171-chr11:5175061..5176633,2	K562	blood:
17	11:5146608-5154908..11:5349791-5355747	K562	blood:
18	chr11:5156441..5158243-chr11:5160175..5163398,3	K562	blood:
19	chr11:5160114..5162229-chr11:5171170..5172711,2	K562	blood:
20	chr11:5143364..5146967-chr11:5150857..5153670,3	K562	blood:
21	chr11:5151076..5153190-chr11:5193820..5196178,2	K562	blood:
22	chr11:5166650..5169776-chr11:5171557..5174439,3	K562	blood:
23	chr11:5150178..5155699-chr11:5220911..5225581,8	K562	blood:
24	chr11:5151017..5154048-chr11:5172575..5176593,5	K562	blood:
25	chr11:5149719..5151749-chr11:5525056..5527952,2	K562	blood:
26	chr11:5169508..5172348-chr11:5506409..5508300,2	K562	blood:
27	chr11:5150699..5153256-chr11:5166471..5169449,2	K562	blood:
28	11:5159254-5162227..11:5700314-5707362	Hela-S3	cervix:
29	chr11:5150699..5153256-chr11:5166471..5169449,2	K562	blood:
30	chr11:5150699..5153690-chr11:5165729..5169449,3	K562	blood:
31	chr11:5111907..5114090-chr11:5149445..5151800,2	K562	blood:
32	chr11:5156441..5158243-chr11:5160175..5163398,3	K562	blood:
33	chr11:5151728..5155807-chr11:5263615..5268276,6	K562	blood:
34	11:5159254-5162227..11:5469844-5475173	H1-hESC	embryonic stem cell:	embryo
35	chr11:5145054..5145634-chr11:5391106..5391649,2	K562	blood:
36	11:5159254-5162227..11:5407716-5412355	H1-hESC	embryonic stem cell:	embryo
37	chr11:5150382..5152243-chr11:5521583..5523771,2	K562	blood:
38	chr11:5167216..5169602-chr11:5170013..5172866,3	K562	blood:
39	chr11:5154058..5156927-chr11:5244271..5247136,2	K562	blood:
40	chr11:5143402..5145661-chr11:5288331..5290238,2	K562	blood:
41	chr11:5163035..5164810-chr11:5166036..5168389,2	K562	blood:
42	chr11:5142801..5144860-chr11:5155280..5157455,2	K562	blood:
43	chr11:5150860..5154299-chr11:5221551..5224711,3	K562	blood:
44	chr11:5166640..5168909-chr11:5173879..5175429,2	K562	blood:
45	chr11:5163035..5164810-chr11:5166036..5168389,2	K562	blood:
46	chr11:5150588..5152755-chr11:5410475..5412093,2	K562	blood:
47	chr11:5155212..5157453-chr11:5171117..5172867,2	K562	blood:
48	chr11:5151592..5153371-chr11:5383918..5386236,2	K562	blood:
49	11:5154908-5159254..11:5407716-5412355	GM12878	blood:
50	chr11:5151510..5153269-chr11:5386500..5388516,2	K562	blood:

No data

Variant related genes	Relation type
OR52A5	TF binding region
OR52A4	TF binding region
OR52A5	CpG island
OR52A4	CpG island
ENSG00000167355	chromatin interactions
ENSG00000187918	chromatin interactions
ENSG00000182070	chromatin interactions
ENSG00000236359	chromatin interactions
ENSG00000226157	chromatin interactions
ENSG00000229988	chromatin interactions
ENSG00000171944	chromatin interactions
ENSG00000221031	chromatin interactions
ENSG00000260629	chromatin interactions
ENSG00000213931	chromatin interactions
ENSG00000176742	chromatin interactions
ENSG00000184698	chromatin interactions
ENSG00000132274	chromatin interactions
ENSG00000196565	chromatin interactions
ENSG00000132256	chromatin interactions
ENSG00000205494	chromatin interactions

Extended variants
information (count: 900 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:900 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11035765	chr11:5143309-5143310	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs545621506	chr11:5143326-5143327	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs150079567	chr11:5143369-5143370	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs551164786	chr11:5143414-5143415	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs562655673	chr11:5143507-5143508	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs138490031	chr11:5143537-5143538	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs533628441	chr11:5143538-5143539	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs112462296	chr11:5143586-5143587	Weak transcription	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs552109146	chr11:5143688-5143689	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs10837379	chr11:5143753-5143754	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs187635655	chr11:5143787-5143788	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs549143233	chr11:5143794-5143795	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs567727632	chr11:5143795-5143796	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs7110809	chr11:5143823-5143824	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs190160307	chr11:5143837-5143838	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs115067009	chr11:5143877-5143878	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs116689619	chr11:5143878-5143879	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs201035774	chr11:5143899-5143900	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs7114854	chr11:5143922-5143923	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs554287778	chr11:5143971-5143972	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs576051767	chr11:5144007-5144008	Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs543550181	chr11:5144059-5144060	Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs200619267	chr11:5144080-5144081	Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs188053796	chr11:5144101-5144102	Weak transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs80270529	chr11:5144154-5144155	Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs66706042	chr11:5144165-5144166	Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs565103246	chr11:5144166-5144167	Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs398114980	chr11:5144174-5144175	Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs111519573	chr11:5144175-5144176	Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs545660557	chr11:5144184-5144185	Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs543284270	chr11:5144251-5144252	Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs528004804	chr11:5144372-5144373	Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs72879624	chr11:5144391-5144392	Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs192569423	chr11:5144393-5144394	Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs531654586	chr11:5144405-5144406	Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs7103864	chr11:5144407-5144408	Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs75003427	chr11:5144409-5144410	Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs182594823	chr11:5144412-5144413	Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs372769254	chr11:5144445-5144446	Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs561895268	chr11:5144453-5144454	Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs75599215	chr11:5144467-5144468	Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs201627553	chr11:5144494-5144495	Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs560490444	chr11:5144498-5144499	Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs536169615	chr11:5144504-5144505	Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs529180601	chr11:5144557-5144558	Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs372399989	chr11:5144558-5144559	Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs116908690	chr11:5144572-5144573	Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs187753106	chr11:5144632-5144633	Weak transcription Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs543492742	chr11:5144636-5144637	Weak transcription Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs558679239	chr11:5144637-5144638	Weak transcription Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:60)

Disease	PMID	Source
Neuroblastoma	18923191	CNVD
Breast cancer	19432969	CNVD
Alzheimer''s disease	17576883	CNVD
Long-qt syndrome	17576883	CNVD
Emphysema	19352772	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Chordoma	18071362	CNVD
Breast cancer	16608533	CNVD
Cancer	21183584	CNVD
Gastric adenocarcinoma	19115996	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	19759907	CNVD
Breast cancer	17603634	CNVD
Medulloblastoma	21979893	CNVD
Thyroid cancer	19087340	CNVD
Melanoma	18172304	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Wilms tumour	21544195	CNVD
Parathyroid adenoma	22454399	CNVD
Chordoma	21602918	CNVD
Breast cancer	21949216	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	19222835	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Beckwith-Wiedemann syndrome	21518781	CNVD
Wilms tumour	21518781	CNVD
Hepatoblastoma	21518781	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Gastric cancer	17908304	CNVD
Barrett''s syndrome	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Multiple myeloma	20724749	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Autism	22495311	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Myelofibrosis	22110671	CNVD
Glioma	17123091	CNVD
Lung cancer	16773561	CNVD
Neuroblastoma	21124317	CNVD
Lung adenocarcinoma	17086460	CNVD
Lung cancer	17086460	CNVD
Schizophrenia	21399695	CNVD
Gastric cancer	16891809	CNVD
Cancer	17160897	CNVD
Multiple myeloma	16616336	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:43 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:5137400-5144000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr11:5139000-5144800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr11:5144000-5144600	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr11:5144600-5145000	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr11:5144800-5145200	Enhancers	K562	blood
6	chr11:5144800-5146800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
7	chr11:5145000-5145800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr11:5145200-5145400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
9	chr11:5145200-5145600	Bivalent Enhancer	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
10	chr11:5145200-5145800	Enhancers	Osteobl	bone
11	chr11:5145200-5146000	Flanking Active TSS	K562	blood
12	chr11:5146000-5147600	Enhancers	K562	blood
13	chr11:5147600-5148000	Weak transcription	K562	blood
14	chr11:5148000-5148400	ZNF genes & repeats	K562	blood
15	chr11:5148400-5150200	Weak transcription	K562	blood
16	chr11:5150200-5151000	Flanking Active TSS	K562	blood
17	chr11:5150400-5151000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
18	chr11:5151000-5152800	Active TSS	K562	blood
19	chr11:5152800-5154000	Flanking Active TSS	K562	blood
20	chr11:5154000-5162400	Weak transcription	K562	blood
21	chr11:5156600-5157000	Enhancers	HUES6 Cell Line	embryonic stem cell
22	chr11:5156600-5157600	Enhancers	iPS-18 Cell Line	embryonic stem cell
23	chr11:5156600-5158400	Enhancers	HUES48 Cell Line	embryonic stem cell
24	chr11:5156600-5159600	Enhancers	ES-I3 Cell Line	embryonic stem cell
25	chr11:5156800-5157000	Enhancers	HUES64 Cell Line	embryonic stem cell
26	chr11:5156800-5157000	Enhancers	iPS-15b Cell Line	embryonic stem cell
27	chr11:5157000-5158200	Weak transcription	HUES6 Cell Line	embryonic stem cell
28	chr11:5157200-5158200	Weak transcription	HUES64 Cell Line	embryonic stem cell
29	chr11:5157200-5158200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
30	chr11:5157600-5158000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
31	chr11:5157600-5158400	Enhancers	Cortex derived primary cultured neurospheres	brain
32	chr11:5157600-5158800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr11:5158000-5159400	Enhancers	iPS-18 Cell Line	embryonic stem cell
34	chr11:5158200-5158600	Enhancers	HUES6 Cell Line	embryonic stem cell
35	chr11:5158200-5158800	Enhancers	iPS-15b Cell Line	embryonic stem cell
36	chr11:5158200-5159800	Enhancers	HUES64 Cell Line	embryonic stem cell
37	chr11:5158400-5159400	Weak transcription	HUES48 Cell Line	embryonic stem cell
38	chr11:5158800-5159400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
39	chr11:5159400-5159600	Enhancers	iPS-15b Cell Line	embryonic stem cell
40	chr11:5159600-5159800	Enhancers	HUES48 Cell Line	embryonic stem cell
41	chr11:5160000-5160600	Enhancers	Fetal Lung	lung
42	chr11:5162400-5162800	Enhancers	K562	blood
43	chr11:5163600-5164600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin

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