Variant report

Variant	nsv528592
Chromosome Location	chr11:73360888-73364673
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	BHLHE40	chr11:73364366-73364620	HepG2	liver:	n/a	n/a
2	BHLHE40	chr11:73361464-73361521	K562	blood:	n/a	n/a
3	CEBPB	chr11:73363395-73363633	HepG2	liver:	n/a	n/a
4	CHD2	chr11:73364044-73364182	HepG2	liver:	n/a	n/a
5	CHD2	chr11:73363315-73363635	HepG2	liver:	n/a	n/a
6	CTCF	chr11:73363180-73363330	HepG2	liver:	n/a	chr11:73363293-73363302
7	ELF1	chr11:73363368-73363761	HepG2	liver:	n/a	n/a
8	EP300	chr11:73363166-73364004	HepG2	liver:	n/a	n/a
9	EP300	chr11:73364257-73364696	HepG2	liver:	n/a	n/a
10	EP300	chr11:73363152-73363892	HepG2	liver:	n/a	n/a
11	FOXA2	chr11:73363302-73363791	HepG2	liver:	n/a	n/a
12	FOXA2	chr11:73364257-73364557	HepG2	liver:	n/a	n/a
13	GATA2	chr11:73360773-73361104	SH-SY5Y	brain:	n/a	chr11:73360957-73360964 chr11:73360957-73360964 chr11:73360957-73360964
14	HDAC2	chr11:73364122-73364527	HepG2	liver:	n/a	n/a
15	HDAC2	chr11:73363212-73363837	HepG2	liver:	n/a	n/a
16	HEY1	chr11:73363120-73363620	HepG2	liver:	n/a	n/a
17	HNF4A	chr11:73363218-73363759	HepG2	liver:	n/a	chr11:73363480-73363492 chr11:73363477-73363495 chr11:73363478-73363493 chr11:73363480-73363492 chr11:73363480-73363492 chr11:73363479-73363492
18	HNF4A	chr11:73363207-73363870	HepG2	liver:	n/a	chr11:73363480-73363492 chr11:73363477-73363495 chr11:73363478-73363493 chr11:73363480-73363492 chr11:73363480-73363492 chr11:73363479-73363492
19	HNF4A	chr11:73363307-73363748	HepG2	liver:	n/a	chr11:73363480-73363492 chr11:73363477-73363495 chr11:73363478-73363493 chr11:73363480-73363492 chr11:73363480-73363492 chr11:73363479-73363492
20	HNF4G	chr11:73363252-73363730	HepG2	liver:	n/a	chr11:73363479-73363494 chr11:73363480-73363492 chr11:73363477-73363495 chr11:73363480-73363492 chr11:73363480-73363492 chr11:73363479-73363492
21	JUND	chr11:73363973-73364073	HepG2	liver:	n/a	n/a
22	MAFF	chr11:73364076-73364251	HepG2	liver:	n/a	n/a
23	MAX	chr11:73363020-73364035	HepG2	liver:	n/a	chr11:73363392-73363402 chr11:73363585-73363594 chr11:73363237-73363246 chr11:73363392-73363402 chr11:73363390-73363403 chr11:73363391-73363402
24	MAX	chr11:73363219-73363611	HepG2	liver:	n/a	chr11:73363392-73363402 chr11:73363585-73363594 chr11:73363237-73363246 chr11:73363392-73363402 chr11:73363390-73363403 chr11:73363391-73363402
25	MAZ	chr11:73363394-73363605	HepG2	liver:	n/a	chr11:73363585-73363594
26	MXI1	chr11:73363387-73363643	H1-hESC	embryonic stem cell:	n/a	chr11:73363393-73363402 chr11:73363581-73363596 chr11:73363393-73363402 chr11:73363579-73363594
27	MXI1	chr11:73363212-73363969	HepG2	liver:	n/a	chr11:73363393-73363402 chr11:73363581-73363596 chr11:73363393-73363402 chr11:73363579-73363594
28	MYBL2	chr11:73362974-73363891	HepG2	liver:	n/a	n/a
29	MYC	chr11:73363364-73363434	MCF-7	breast:	n/a	chr11:73363392-73363402 chr11:73363392-73363402 chr11:73363390-73363403 chr11:73363391-73363402
30	MYC	chr11:73363219-73363689	HepG2	liver:	n/a	chr11:73363392-73363402 chr11:73363585-73363594 chr11:73363237-73363246 chr11:73363392-73363402 chr11:73363390-73363403 chr11:73363391-73363402
31	MYC	chr11:73363197-73363201	HepG2	liver:	n/a	n/a
32	NFIC	chr11:73363052-73363904	HepG2	liver:	n/a	n/a
33	POLR2A	chr11:73361348-73361352	HepG2	liver:	n/a	n/a
34	POLR2A	chr11:73360915-73360967	HepG2	liver:	n/a	n/a
35	POLR2A	chr11:73363150-73363769	HepG2	liver:	n/a	n/a
36	POLR2A	chr11:73360994-73361020	HepG2	liver:	n/a	n/a
37	POLR2A	chr11:73363965-73364804	HepG2	liver:	n/a	n/a
38	POLR2A	chr11:73362814-73362907	HepG2	liver:	n/a	n/a
39	POLR2A	chr11:73362666-73362798	HepG2	liver:	n/a	n/a
40	POLR2A	chr11:73361264-73361453	HepG2	liver:	n/a	n/a
41	POLR2A	chr11:73363074-73363145	HepG2	liver:	n/a	n/a
42	POLR2A	chr11:73363935-73364317	K562	blood:	n/a	n/a
43	POLR2A	chr11:73362925-73363515	K562	blood:	n/a	n/a
44	POLR2A	chr11:73363171-73363962	HepG2	liver:	n/a	n/a
45	POLR2A	chr11:73363272-73363748	HepG2	liver:	n/a	n/a
46	POLR2A	chr11:73360773-73362423	K562	blood:	n/a	n/a
47	POLR2A	chr11:73361686-73362016	HepG2	liver:	n/a	n/a
48	POLR2A	chr11:73361780-73361923	HepG2	liver:	n/a	n/a
49	POLR2A	chr11:73361145-73361329	HepG2	liver:	n/a	n/a
50	POLR2A	chr11:73362842-73363006	HepG2	liver:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:73362898-73362948	HRE	kidney:	n/a
2	chr11:73362898-73362948	A549	lung:	n/a
3	chr11:73362898-73362948	GM19239	blood:	n/a
4	chr11:73362898-73362948	HPAEpiC	pulmonary alveolar:	n/a
5	chr11:73362898-73362948	NT2-D1	testis:	n/a
6	chr11:73362898-73362948	Caco-2	colon:	n/a
7	chr11:73362898-73362948	HL-60	blood:	n/a
8	chr11:73362898-73362948	NH-A	brain:	n/a
9	chr11:73362898-73362948	Jurkat	blood:	n/a
10	chr11:73362898-73362948	MCF-7	breast:	n/a
11	chr11:73362898-73362948	GM06990	blood:	n/a
12	chr11:73362898-73362948	U87	brain:	n/a
13	chr11:73362898-73362948	BJ	skin:	n/a
14	chr11:73362898-73362948	SK-N-SH	brain:	n/a
15	chr11:73362898-73362948	ovcar-3	ovarian:	n/a
16	chr11:73362898-73362948	SAEC	small airway:	n/a
17	chr11:73362898-73362948	HIPEpiC	eye:	n/a
18	chr11:73362898-73362948	Hela-S3	cervix:	n/a
19	chr11:73362898-73362948	HNPCEpiC	eye:	n/a
20	chr11:73362898-73362948	HCPEpiC	choroid plexus:	n/a
21	chr11:73362898-73362948	PFSK-1	brain:	n/a
22	chr11:73362898-73362948	AG04450	lung:	fetal
23	chr11:73362898-73362948	ProgFib	skin:	n/a
24	chr11:73362898-73362948	GM12892	blood:	n/a
25	chr11:73362898-73362948	GM12878	blood:	n/a
26	chr11:73362898-73362948	PANC-1	pancreas:	n/a
27	chr11:73362898-73362948	IMR90	lung:	fetal
28	chr11:73362898-73362948	ECC-1	luminal epithelium:	n/a
29	chr11:73362898-73362948	HCT-116	colon:	n/a
30	chr11:73362898-73362948	AG10803	skin:	n/a
31	chr11:73362898-73362948	HUVEC	blood vessel:	n/a
32	chr11:73362898-73362948	HRPEpiC	eye:	n/a
33	chr11:73362898-73362948	NB4	blood:	n/a
34	chr11:73362898-73362948	T-47D	breast:	n/a
35	chr11:73362898-73362948	GM12891	blood:	n/a
36	chr11:73362898-73362948	Hepatocyte	liver:	n/a
37	chr11:73362898-73362948	HRCEpiC	kidney:	n/a
38	chr11:73362898-73362948	NHDF-neo	bronchial:	n/a
39	chr11:73362898-73362948	HCM	heart:	n/a
40	chr11:73362898-73362948	HEEpiC	esophagus:	n/a
41	chr11:73362898-73362948	CMK	blood:	n/a
42	chr11:73362898-73362948	SK-N-MC	brain:	n/a
43	chr11:73362898-73362948	NHBE	bronchial:	n/a
44	chr11:73362898-73362948	MCF10A-Er-Src	breast:	n/a
45	chr11:73362898-73362948	HEK293	kidney:	embryo
46	chr11:73362898-73362948	AG09319	gingival:	n/a
47	chr11:73362898-73362948	HepG2	liver:	n/a
48	chr11:73362898-73362948	AG09309	skin:	n/a
49	chr11:73362898-73362948	AG04449	skin:	fetal
50	chr11:73362898-73362948	SK-N-SH_RA	brain:	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr11:73360291..73363163-chr11:73370092..73372185,2	MCF-7	breast:
2	chr11:73361371..73362170-chr11:73372091..73372630,2	K562	blood:

Variant related genes	Relation type
PLEKHB1	TF binding region
PLEKHB1	CpG island
ENSG00000021300	chromatin interactions

Extended variants
information (count: 170 )
Associated
traits (count: 103 )

Variant overlapped rSNPs/rCNVs (count:170 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs652229	chr11:73360888-73360889	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs535667567	chr11:73361013-73361014	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs182453746	chr11:73361016-73361017	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs11603005	chr11:73361067-73361068	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs141567127	chr11:73361114-73361115	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs188563879	chr11:73361130-73361131	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs553774887	chr11:73361131-73361132	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs576869144	chr11:73361210-73361211	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs115043881	chr11:73361243-73361244	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs543496798	chr11:73361257-73361258	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs581888	chr11:73361265-73361266	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs531582719	chr11:73361267-73361268	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs193098861	chr11:73361275-73361276	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs148396009	chr11:73361279-73361280	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs527552553	chr11:73361316-73361317	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs183261268	chr11:73361319-73361320	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs570469919	chr11:73361320-73361321	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs73536609	chr11:73361322-73361323	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs189076056	chr11:73361407-73361408	Weak transcription Enhancers Strong transcription Bivalent/Poised TSS Genic enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs570029130	chr11:73361411-73361412	Weak transcription Enhancers Strong transcription Bivalent/Poised TSS Genic enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs536078943	chr11:73361413-73361414	Weak transcription Enhancers Strong transcription Bivalent/Poised TSS Genic enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs532743266	chr11:73361467-73361468	Weak transcription Enhancers Strong transcription Bivalent/Poised TSS Genic enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs370101841	chr11:73361480-73361481	Weak transcription Enhancers Strong transcription Bivalent/Poised TSS Genic enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs555963446	chr11:73361511-73361512	Weak transcription Enhancers Strong transcription Bivalent/Poised TSS Genic enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs377048250	chr11:73361555-73361556	Weak transcription Enhancers Strong transcription Bivalent/Poised TSS Genic enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs368105555	chr11:73361577-73361578	Weak transcription Enhancers Strong transcription Bivalent/Poised TSS Genic enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs371673275	chr11:73361592-73361593	Weak transcription Enhancers Strong transcription Bivalent/Poised TSS Genic enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs375874055	chr11:73361595-73361596	Weak transcription Enhancers Strong transcription Bivalent/Poised TSS Genic enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs535288456	chr11:73361603-73361604	Weak transcription Enhancers Strong transcription Bivalent Enhancer Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs368856276	chr11:73361609-73361610	Weak transcription Enhancers Strong transcription Bivalent Enhancer Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs200815196	chr11:73361610-73361611	Weak transcription Enhancers Strong transcription Bivalent Enhancer Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs576815673	chr11:73361612-73361613	Weak transcription Enhancers Strong transcription Bivalent Enhancer Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs545480416	chr11:73361613-73361614	Weak transcription Enhancers Strong transcription Bivalent Enhancer Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs375308321	chr11:73361621-73361622	Weak transcription Enhancers Strong transcription Bivalent Enhancer Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs576020398	chr11:73361625-73361626	Weak transcription Enhancers Strong transcription Bivalent Enhancer Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs369788651	chr11:73361687-73361688	Weak transcription Enhancers Strong transcription Bivalent Enhancer Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs541641714	chr11:73361716-73361717	Weak transcription Enhancers Strong transcription Bivalent Enhancer Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs201491574	chr11:73361721-73361722	Weak transcription Enhancers Strong transcription Bivalent Enhancer Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs118064377	chr11:73361735-73361736	Weak transcription Enhancers Strong transcription Bivalent Enhancer Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs376741198	chr11:73361745-73361746	Weak transcription Enhancers Strong transcription Bivalent Enhancer Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs111810999	chr11:73361751-73361752	Weak transcription Enhancers Strong transcription Bivalent Enhancer Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs199893863	chr11:73361762-73361763	Weak transcription Enhancers Strong transcription Bivalent Enhancer Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs7940286	chr11:73361781-73361782	Weak transcription Enhancers Strong transcription Bivalent Enhancer Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs112058787	chr11:73361787-73361788	Weak transcription Enhancers Strong transcription Bivalent Enhancer Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs370192996	chr11:73361789-73361790	Weak transcription Enhancers Strong transcription Bivalent Enhancer Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs117211429	chr11:73361797-73361798	Weak transcription Enhancers Strong transcription Bivalent Enhancer Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs376185930	chr11:73361798-73361799	Weak transcription Enhancers Strong transcription Bivalent Enhancer Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs75062765	chr11:73361803-73361804	Weak transcription Enhancers Strong transcription Bivalent Enhancer Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs563821159	chr11:73361812-73361813	Weak transcription Enhancers Strong transcription Bivalent Enhancer Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs529342734	chr11:73361826-73361827	Weak transcription Enhancers Strong transcription Bivalent Enhancer Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:103)

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
Acute myeloid leukemia	20729466	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
Acute lymphoblastic leukemia	20435627	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Prostate cancer	18632612	CNVD
Smith-Lemli-Opitz syndrome	21572526	CNVD
Glioblastoma multiforme	21080181	CNVD
Multiple myeloma	16461302	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Chordoma	21602918	CNVD
Metanephric adenoma	20802469	CNVD
Melanoma	18172304	CNVD
Breast cancer	21806811	CNVD
Breast cancer	22002566	CNVD
Ductal carcinoma	18381933	CNVD
Retinoblastoma	22278416	CNVD
Breast cancer	20953835	CNVD
oto-dental syndrome	17656375	CNVD
Asthma	21956041	CNVD
Breast cancer	17603634	CNVD
Ovarian neoplasms	16753589	CNVD
Non-small cell lung cancer	20864512	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cervical cancer	21062161	CNVD
Breast cancer	21509527	CNVD
Breast cancer	17001317	CNVD
Oral squamous cell carcinoma	16619035	CNVD
Intracranial aneurysm	16715129	CNVD
Colorectal cancer	16272173	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Colorectal cancer	16882699	CNVD
Berardinelli-seip congenital generalized lipodystrophy	17668395	CNVD
Spinal muscular atrophy	17668395	CNVD
Neonatal seizures	17668395	CNVD
Neonatal seizures	17668391	CNVD
Neuroticism	17667963	CNVD
Cancer	17916600	CNVD
Squamous cell cancer	19047905	CNVD
Multiple endocrine neoplasia type 1	19566914	CNVD
XY sex reversal	17503084	CNVD
Berardinelli-seip congenital generalized lipodystrophy	17668391	CNVD
Maculopathy	17646752	CNVD
Breast cancer	17899364	CNVD
Breast cancer	17157792	CNVD
Esophageal squamous carcinoma	18350619	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Breast cancer	21364760	CNVD
lymphocytic leukemia	21291569	CNVD
Myelofibrosis	22110671	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Cancer	22183965	CNVD
Melanoma	22183965	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Breast cancer	16620391	CNVD
Multiple myeloma	17550852	CNVD
Neuroblastoma	18923191	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Lung cancer	18438408	CNVD
Multiple myeloma	16616336	CNVD
Urothelial cell carcinoma	18451213	CNVD
Leukoplakia	24403051	CNVD
Prostate cancer	17217626	CNVD
Cancer	22429812	CNVD
small cell lung cancer	20016488	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	17142309	CNVD
Lung cancer	21203850	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:180 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:73357200-73364000	Weak transcription	Liver	Liver
2	chr11:73357800-73364200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
3	chr11:73358200-73361000	Flanking Active TSS	HepG2	liver
4	chr11:73358600-73363200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
5	chr11:73359000-73361000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr11:73359000-73363200	Weak transcription	Right Atrium	heart
7	chr11:73359000-73371600	Weak transcription	Fetal Brain Female	brain
8	chr11:73359000-73371600	Weak transcription	Right Ventricle	heart
9	chr11:73359200-73361000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr11:73359200-73361800	Weak transcription	Primary T cells from cord blood	blood
11	chr11:73359200-73362200	Weak transcription	Fetal Intestine Small	intestine
12	chr11:73359200-73362600	Weak transcription	HMEC	breast
13	chr11:73359200-73362800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
14	chr11:73359200-73362800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr11:73359200-73362800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
16	chr11:73359200-73362800	Weak transcription	Gastric	stomach
17	chr11:73359200-73363000	Weak transcription	Brain Germinal Matrix	brain
18	chr11:73359200-73363200	Weak transcription	H9 Cell Line	embryonic stem cell
19	chr11:73359200-73363200	Weak transcription	Rectal Mucosa Donor 31	rectum
20	chr11:73359200-73367200	Weak transcription	Spleen	Spleen
21	chr11:73359200-73371600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
22	chr11:73359200-73371600	Weak transcription	Thymus	Thymus
23	chr11:73359200-73371800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
24	chr11:73359400-73362600	Weak transcription	Pancreas	Pancrea
25	chr11:73359400-73363000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
26	chr11:73359400-73363400	Weak transcription	Stomach Mucosa	stomach
27	chr11:73359400-73367000	Weak transcription	Lung	lung
28	chr11:73359400-73371800	Weak transcription	Duodenum Smooth Muscle	Duodenum
29	chr11:73359600-73361600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
30	chr11:73359600-73362800	Weak transcription	Primary T helper cells fromperipheralblood	blood
31	chr11:73359600-73363400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
32	chr11:73359600-73372200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
33	chr11:73359800-73362800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
34	chr11:73359800-73362800	Weak transcription	Primary T helper cells PMA-I stimulated	--
35	chr11:73359800-73363200	Weak transcription	HUES48 Cell Line	embryonic stem cell
36	chr11:73359800-73371800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
37	chr11:73359800-73371800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
38	chr11:73360000-73361400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
39	chr11:73360000-73361400	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
40	chr11:73360000-73363000	Weak transcription	Primary T cells fromperipheralblood	blood
41	chr11:73360200-73363200	Weak transcription	HUES64 Cell Line	embryonic stem cell
42	chr11:73360400-73361200	Weak transcription	Brain Angular Gyrus	brain
43	chr11:73360400-73361600	Weak transcription	Cortex derived primary cultured neurospheres	brain
44	chr11:73360400-73361600	Enhancers	Brain Cingulate Gyrus	brain
45	chr11:73360400-73362800	Weak transcription	H1 Cell Line	embryonic stem cell
46	chr11:73360400-73363000	Enhancers	Brain Hippocampus Middle	brain
47	chr11:73360600-73361000	Enhancers	Brain Inferior Temporal Lobe	brain
48	chr11:73360600-73362400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr11:73360600-73362400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
50	chr11:73360600-73362800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell

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