Variant report

Variant	esv1833978
Chromosome Location	chr11:59377543-59383631
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:715)
CpG islands
(count:672)
Chromatin interactive
region (count:36)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:715 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:59383156-59384444	K562	blood:	n/a	n/a
2	ARID3A	chr11:59383035-59384303	HepG2	liver:	n/a	n/a
3	ATF1	chr11:59383083-59384181	K562	blood:	n/a	n/a
4	ATF2	chr11:59383077-59384207	GM12878	blood:	n/a	n/a
5	ATF2	chr11:59383226-59384152	GM12878	blood:	n/a	n/a
6	ATF2	chr11:59383222-59383838	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF3	chr11:59383325-59383804	A549	lung:	n/a	chr11:59383589-59383609
8	ATF3	chr11:59383031-59383774	K562	blood:	n/a	chr11:59383244-59383253 chr11:59383589-59383609
9	ATF3	chr11:59383151-59383466	H1-hESC	embryonic stem cell:	n/a	chr11:59383244-59383253
10	BACH1	chr11:59383325-59383851	H1-hESC	embryonic stem cell:	n/a	n/a
11	BATF	chr11:59379585-59379964	GM12878	blood:	n/a	n/a
12	BATF	chr11:59383379-59383785	GM12878	blood:	n/a	n/a
13	BATF	chr11:59377874-59378142	GM12878	blood:	n/a	n/a
14	BHLHE40	chr11:59383143-59384256	K562	blood:	n/a	chr11:59383252-59383268
15	BHLHE40	chr11:59383108-59384395	GM12878	blood:	n/a	chr11:59383252-59383268
16	BHLHE40	chr11:59382040-59382371	K562	blood:	n/a	n/a
17	BHLHE40	chr11:59383514-59384214	A549	lung:	n/a	n/a
18	BHLHE40	chr11:59379855-59379926	A549	lung:	n/a	n/a
19	BHLHE40	chr11:59382742-59382817	GM12878	blood:	n/a	n/a
20	BRCA1	chr11:59383094-59383608	HepG2	liver:	n/a	n/a
21	BRCA1	chr11:59383112-59384130	Hela-S3	cervix:	n/a	n/a
22	BRCA1	chr11:59383200-59383711	H1-hESC	embryonic stem cell:	n/a	n/a
23	BRCA1	chr11:59383149-59383924	GM12878	blood:	n/a	n/a
24	CBX3	chr11:59383082-59384392	K562	blood:	n/a	n/a
25	CCNT2	chr11:59382240-59383537	K562	blood:	n/a	chr11:59382575-59382584 chr11:59382536-59382556
26	CEBPB	chr11:59383209-59384082	Hela-S3	cervix:	n/a	chr11:59383540-59383548
27	CEBPB	chr11:59383491-59383987	K562	blood:	n/a	chr11:59383540-59383548
28	CEBPB	chr11:59380707-59380765	K562	blood:	n/a	chr11:59380730-59380743
29	CEBPB	chr11:59382578-59382831	Hela-S3	cervix:	n/a	n/a
30	CEBPB	chr11:59383213-59384087	IMR90	lung:	n/a	chr11:59383540-59383548
31	CEBPB	chr11:59381041-59381056	K562	blood:	n/a	n/a
32	CEBPZ	chr11:59383181-59384028	HepG2	liver:	n/a	n/a
33	CHD1	chr11:59383039-59383364	GM12878	blood:	n/a	n/a
34	CHD1	chr11:59382474-59382715	GM12878	blood:	n/a	n/a
35	CHD2	chr11:59382604-59382819	K562	blood:	n/a	n/a
36	CHD2	chr11:59382454-59384139	Hela-S3	cervix:	n/a	n/a
37	CHD2	chr11:59383088-59383953	HepG2	liver:	n/a	n/a
38	CHD2	chr11:59382523-59382832	HepG2	liver:	n/a	n/a
39	CHD2	chr11:59382402-59382798	GM12878	blood:	n/a	n/a
40	CHD2	chr11:59383015-59384265	GM12878	blood:	n/a	n/a
41	CHD2	chr11:59383093-59384133	K562	blood:	n/a	n/a
42	CHD2	chr11:59383074-59384025	H1-hESC	embryonic stem cell:	n/a	n/a
43	CHD2	chr11:59382682-59382871	H1-hESC	embryonic stem cell:	n/a	n/a
44	CREB1	chr11:59382974-59383997	H1-hESC	embryonic stem cell:	n/a	chr11:59383587-59383600
45	CREB1	chr11:59382593-59384228	GM12878	blood:	n/a	chr11:59383587-59383600
46	CREB1	chr11:59382973-59384301	GM12878	blood:	n/a	chr11:59383587-59383600
47	CREB1	chr11:59382924-59384031	A549	lung:	n/a	chr11:59383587-59383600
48	CREB1	chr11:59383028-59383943	A549	lung:	n/a	chr11:59383587-59383600
49	CREB1	chr11:59382530-59384146	HepG2	liver:	n/a	chr11:59383587-59383600
50	CREB1	chr11:59382981-59384124	ECC-1	luminal epithelium:	n/a	chr11:59383587-59383600

(count:672 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:59383068-59383118	HCPEpiC	choroid plexus:	n/a
2	chr11:59383068-59383118	HCPEpiC	choroid plexus:	n/a
3	chr11:59382818-59382868	HCPEpiC	choroid plexus:	n/a
4	chr11:59383203-59383253	NB4	blood:	n/a
5	chr11:59383068-59383118	AG04450	lung:	fetal
6	chr11:59382818-59382868	HCF	heart:	n/a
7	chr11:59382758-59382808	PrEC	prostate:	n/a
8	chr11:59382758-59382808	HCF	heart:	n/a
9	chr11:59383312-59383362	NH-A	brain:	n/a
10	chr11:59383409-59383459	HUVEC	blood vessel:	n/a
11	chr11:59383068-59383118	K562	blood:	n/a
12	chr11:59382758-59382808	BE2_C	brain:	n/a
13	chr11:59383312-59383362	U87	brain:	n/a
14	chr11:59383312-59383362	Jurkat	blood:	n/a
15	chr11:59383068-59383118	GM12892	blood:	n/a
16	chr11:59383068-59383118	HNPCEpiC	eye:	n/a
17	chr11:59380676-59380726	RPTEC	kidney:	n/a
18	chr11:59382818-59382868	HRPEpiC	eye:	n/a
19	chr11:59382877-59382927	T-47D	breast:	n/a
20	chr11:59382758-59382808	AoSMC	blood vessel:	n/a
21	chr11:59380676-59380726	Jurkat	blood:	n/a
22	chr11:59382758-59382808	SK-N-SH	brain:	n/a
23	chr11:59383068-59383118	GM12891	blood:	n/a
24	chr11:59383312-59383362	HCPEpiC	choroid plexus:	n/a
25	chr11:59382296-59382346	HRPEpiC	eye:	n/a
26	chr11:59382818-59382868	NHDF-neo	bronchial:	n/a
27	chr11:59383312-59383362	NHDF-neo	bronchial:	n/a
28	chr11:59383203-59383253	HRCEpiC	kidney:	n/a
29	chr11:59380676-59380726	K562	blood:	n/a
30	chr11:59383068-59383118	H1-hESC	embryonic stem cell:	embryo
31	chr11:59383409-59383459	HRE	kidney:	n/a
32	chr11:59383312-59383362	PFSK-1	brain:	n/a
33	chr11:59383312-59383362	MCF-7	breast:	n/a
34	chr11:59378927-59378977	GM12891	blood:	n/a
35	chr11:59383578-59383628	MCF-7	breast:	n/a
36	chr11:59382818-59382868	PrEC	prostate:	n/a
37	chr11:59383203-59383253	ECC-1	luminal epithelium:	n/a
38	chr11:59383578-59383628	HCT-116	colon:	n/a
39	chr11:59383409-59383459	A549	lung:	n/a
40	chr11:59383203-59383253	AoSMC	blood vessel:	n/a
41	chr11:59383578-59383628	ovcar-3	ovarian:	n/a
42	chr11:59382818-59382868	ECC-1	luminal epithelium:	n/a
43	chr11:59383409-59383459	H1-hESC	embryonic stem cell:	embryo
44	chr11:59382877-59382927	BE2_C	brain:	n/a
45	chr11:59382758-59382808	GM12878	blood:	n/a
46	chr11:59383409-59383459	AG10803	skin:	n/a
47	chr11:59383578-59383628	LNCaP	prostate:	n/a
48	chr11:59383203-59383253	ProgFib	skin:	n/a
49	chr11:59380676-59380726	MCF10A-Er-Src	breast:	n/a
50	chr11:59383068-59383118	HCT-116	colon:	n/a

(count:36 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:59362508..59365255-chr11:59378234..59380693,3	K562	blood:
2	chr11:59364283..59366462-chr11:59380493..59382759,2	MCF-7	breast:
3	chr11:59372664..59374288-chr11:59375717..59377939,2	MCF-7	breast:
4	chr11:59379146..59381021-chr11:59381463..59383297,2	MCF-7	breast:
5	chr11:59381028..59383632-chr11:59387004..59389826,3	K562	blood:
6	chr11:59327475..59330060-chr11:59381628..59383602,2	K562	blood:
7	chr11:59367491..59370423-chr11:59380896..59384148,4	K562	blood:
8	chr11:59381899..59384726-chr11:59386703..59391439,4	MCF-7	breast:
9	chr11:59324538..59326283-chr11:59383295..59385264,2	K562	blood:
10	chr11:59380994..59383091-chr11:59446545..59448432,2	K562	blood:
11	chr11:59382737..59383278-chr13:111365369..111365914,2	Hela-S3	cervix:
12	chr11:59381725..59384642-chr11:59521273..59522941,2	K562	blood:
13	chr11:59332513..59335346-chr11:59377143..59379065,2	K562	blood:
14	chr11:59379949..59382151-chr11:59418599..59421025,2	MCF-7	breast:
15	chr11:59322188..59323808-chr11:59380792..59382700,2	K562	blood:
16	chr11:59358338..59361390-chr11:59376004..59379219,3	K562	blood:
17	chr11:59340962..59342782-chr11:59376375..59380389,3	K562	blood:
18	chr11:59373266..59379105-chr11:59379660..59383510,5	MCF-7	breast:
19	chr11:59309329..59311189-chr11:59379194..59381372,2	K562	blood:
20	chr11:59379597..59385439-chr11:59434812..59438230,12	K562	blood:
21	chr11:59380013..59385486-chr11:59434648..59438262,9	MCF-7	breast:
22	chr11:59370209..59373051-chr11:59379032..59380863,2	MCF-7	breast:
23	chr11:59379146..59381021-chr11:59381463..59383297,2	MCF-7	breast:
24	chr11:59359890..59361543-chr11:59376004..59377762,2	K562	blood:
25	chr11:59382728..59383524-chr6:31783159..31783746,2	Hela-S3	cervix:
26	chr11:59382346..59384021-chr11:59576839..59579644,2	K562	blood:
27	chr11:59382734..59385576-chr11:59440781..59442919,2	K562	blood:
28	chr11:59369187..59371019-chr11:59381585..59383481,2	MCF-7	breast:
29	chr11:59373266..59379105-chr11:59379660..59383510,5	MCF-7	breast:
30	chr11:59381143..59385193-chr11:59434975..59438411,10	K562	blood:
31	chr11:59322976..59324823-chr11:59375645..59377849,2	K562	blood:
32	chr1:23670573..23671130-chr11:59382477..59382982,2	Hela-S3	cervix:
33	chr11:59332034..59337600-chr11:59380778..59383923,5	K562	blood:
34	chr11:59367319..59373347-chr11:59375671..59384148,16	K562	blood:
35	chr11:59357778..59359857-chr11:59379899..59383236,3	K562	blood:
36	chr11:59379168..59382086-chr11:59390043..59391768,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-STX3-2	chr11:59383619-59385512	NONHSAT021532

No data

Variant related genes	Relation type
ENSG00000255139	TF binding region
OSBP	TF binding region
ENSG00000255139	CpG island
OSBP	CpG island
ENSG00000110048	chromatin interactions
ENSG00000255139	chromatin interactions
ENSG00000204390	chromatin interactions
ENSG00000166889	chromatin interactions
ENSG00000166902	chromatin interactions
ENSG00000264559	chromatin interactions
ENSG00000204389	chromatin interactions
ENSG00000254477	chromatin interactions
ENSG00000252893	chromatin interactions
ENSG00000134905	chromatin interactions
ENSG00000166900	chromatin interactions
ENSG00000125944	chromatin interactions
ENSG00000255008	chromatin interactions
ENSG00000153487	chromatin interactions
ENSG00000255355	chromatin interactions

Extended variants
information (count: 210 )
Associated
traits (count: 54 )

Variant overlapped rSNPs/rCNVs (count:210 , 50 per page) page: 1 2 3 4 5

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11603417	chr11:59377543-59377544	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs548978639	chr11:59377659-59377660	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs567310421	chr11:59377670-59377671	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs186641969	chr11:59377686-59377687	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs144947669	chr11:59377700-59377701	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs569312108	chr11:59377728-59377729	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs192751813	chr11:59377729-59377730	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs557941273	chr11:59377782-59377783	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs184627635	chr11:59377783-59377784	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs17593682	chr11:59377788-59377789	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
11	rs539412273	chr11:59377819-59377820	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs369926026	chr11:59377848-59377849	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs2228289	chr11:59377858-59377859	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs61755078	chr11:59377903-59377904	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs537706135	chr11:59377938-59377939	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs373860788	chr11:59377989-59377990	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs376305185	chr11:59378006-59378007	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs112406959	chr11:59378017-59378018	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs370549484	chr11:59378023-59378024	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs375768205	chr11:59378062-59378063	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs199694782	chr11:59378104-59378105	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs577730735	chr11:59378123-59378124	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs545211353	chr11:59378196-59378197	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs73486920	chr11:59378198-59378199	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs554201956	chr11:59378241-59378242	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs192769832	chr11:59378249-59378250	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs542790229	chr11:59378257-59378258	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs80118645	chr11:59378271-59378272	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs112427933	chr11:59378272-59378273	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs74601153	chr11:59378288-59378289	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs61595958	chr11:59378289-59378290	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs570831115	chr11:59378291-59378292	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs539856823	chr11:59378325-59378326	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs76951138	chr11:59378339-59378340	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs550955142	chr11:59378349-59378350	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs184294311	chr11:59378390-59378391	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs533483245	chr11:59378404-59378405	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs189117420	chr11:59378410-59378411	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs566766383	chr11:59378424-59378425	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs7129604	chr11:59378491-59378492	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs7128845	chr11:59378540-59378541	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs145905102	chr11:59378561-59378562	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs35074206	chr11:59378608-59378609	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs201238538	chr11:59378609-59378610	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs538256381	chr11:59378661-59378662	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs556158264	chr11:59378665-59378666	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs576614058	chr11:59378767-59378768	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs534696286	chr11:59378840-59378841	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs538592750	chr11:59378844-59378845	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs554003864	chr11:59378872-59378873	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:54)

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
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:826 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:59334200-59382000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr11:59340800-59378200	Strong transcription	Fetal Thymus	thymus
3	chr11:59342000-59379000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
4	chr11:59342200-59378200	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
5	chr11:59343600-59378400	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
6	chr11:59343800-59382000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr11:59350200-59378200	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
8	chr11:59352400-59378000	Strong transcription	Sigmoid Colon	Sigmoid Colon
9	chr11:59352600-59378200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chr11:59352800-59378400	Strong transcription	Primary monocytes fromperipheralblood	blood
11	chr11:59353200-59377800	Strong transcription	Fetal Muscle Trunk	muscle
12	chr11:59353200-59378200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
13	chr11:59353200-59378400	Strong transcription	Primary hematopoietic stem cells short term culture	blood
14	chr11:59353400-59378000	Strong transcription	Fetal Intestine Large	intestine
15	chr11:59353400-59378200	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
16	chr11:59353400-59378200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
17	chr11:59353400-59378800	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
18	chr11:59353600-59378200	Strong transcription	HUES6 Cell Line	embryonic stem cell
19	chr11:59353600-59378600	Strong transcription	Monocytes-CD14+_RO01746	blood
20	chr11:59353800-59378200	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
21	chr11:59353800-59378200	Strong transcription	Duodenum Mucosa	Duodenum
22	chr11:59353800-59378400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
23	chr11:59353800-59379400	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
24	chr11:59354200-59378200	Strong transcription	HUES64 Cell Line	embryonic stem cell
25	chr11:59354400-59379400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr11:59354600-59379600	Strong transcription	Thymus	Thymus
27	chr11:59354800-59378200	Strong transcription	Rectal Mucosa Donor 29	rectum
28	chr11:59354800-59378400	Strong transcription	Dnd41	blood
29	chr11:59355600-59378000	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
30	chr11:59355800-59379800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
31	chr11:59357200-59378200	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
32	chr11:59357400-59378200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr11:59357400-59379000	Strong transcription	GM12878-XiMat	blood
34	chr11:59357600-59378000	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
35	chr11:59357600-59378200	Strong transcription	iPS-18 Cell Line	embryonic stem cell
36	chr11:59357600-59378200	Strong transcription	Primary B cells from peripheral blood	blood
37	chr11:59357600-59378200	Strong transcription	Rectal Mucosa Donor 31	rectum
38	chr11:59357600-59378200	Strong transcription	HUVEC	blood vessel
39	chr11:59357600-59379200	Strong transcription	K562	blood
40	chr11:59357800-59380600	Strong transcription	Primary B cells from cord blood	blood
41	chr11:59358000-59378200	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
42	chr11:59358400-59382000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
43	chr11:59358800-59378400	Strong transcription	Osteobl	bone
44	chr11:59359200-59378200	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
45	chr11:59359200-59378200	Strong transcription	Primary T cells from cord blood	blood
46	chr11:59359200-59378200	Strong transcription	Colonic Mucosa	Colon
47	chr11:59359200-59378600	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
48	chr11:59360400-59378000	Strong transcription	Duodenum Smooth Muscle	Duodenum
49	chr11:59363400-59378200	Strong transcription	Fetal Brain Female	brain
50	chr11:59364000-59378000	Strong transcription	Cortex derived primary cultured neurospheres	brain

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