Variant report

Variant	nsv8840
Chromosome Location	chr11:74553861-74558956
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:241)
CpG islands
(count:61)
Chromatin interactive
region (count:13)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:241 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CCNT2	chr11:74554094-74554356	K562	blood:	n/a	n/a
2	CEBPB	chr11:74555376-74555400	K562	blood:	n/a	n/a
3	CEBPB	chr11:74555234-74555539	IMR90	lung:	n/a	n/a
4	CTCF	chr11:74553986-74554184	HepG2	liver:	n/a	n/a
5	CTCF	chr11:74554080-74554230	RPTEC	kidney:	n/a	n/a
6	CTCF	chr11:74554020-74554194	GM19239	blood:	n/a	n/a
7	CTCF	chr11:74554000-74554150	HUVEC	blood vessel:	n/a	n/a
8	CTCF	chr11:74557940-74558090	HEEpiC	esophagus:	n/a	n/a
9	CTCF	chr11:74553980-74554130	AG04450	lung:	n/a	n/a
10	CTCF	chr11:74557980-74558130	HMF	breast:	n/a	n/a
11	CTCF	chr11:74554000-74554150	GM12873	blood:	n/a	n/a
12	CTCF	chr11:74553980-74554130	HepG2	liver:	n/a	n/a
13	CTCF	chr11:74554033-74554174	Hela-S3	cervix:	n/a	n/a
14	CTCF	chr11:74557940-74558090	HRPEpiC	eye:	n/a	n/a
15	CTCF	chr11:74557920-74558070	AG09319	gingival:	n/a	n/a
16	CTCF	chr11:74557940-74558090	AG09309	skin:	n/a	n/a
17	CTCF	chr11:74557980-74558130	SAEC	small airway:	n/a	n/a
18	CTCF	chr11:74554014-74554196	A549	lung:	n/a	n/a
19	CTCF	chr11:74554056-74554186	GM10266	blood:	n/a	n/a
20	CTCF	chr11:74557940-74558090	HBMEC	blood vessel:	n/a	n/a
21	CTCF	chr11:74553980-74554130	WERI-Rb-1	eye:	n/a	n/a
22	CTCF	chr11:74554000-74554150	Caco-2	colon:	n/a	n/a
23	CTCF	chr11:74557920-74558070	AoAF	blood vessel:	n/a	n/a
24	CTCF	chr11:74553996-74554208	MCF-7	breast:	n/a	n/a
25	CTCF	chr11:74557960-74558110	AoAF	blood vessel:	n/a	n/a
26	CTCF	chr11:74554000-74554150	GM12872	blood:	n/a	n/a
27	CTCF	chr11:74554020-74554170	HBMEC	blood vessel:	n/a	n/a
28	CTCF	chr11:74557920-74558070	HPF	lung:	n/a	n/a
29	CTCF	chr11:74557920-74558070	HBMEC	blood vessel:	n/a	n/a
30	CTCF	chr11:74554035-74554153	Fibrobl	skin:	n/a	n/a
31	CTCF	chr11:74554000-74554150	HFF-Myc	foreskin:	n/a	n/a
32	CTCF	chr11:74554040-74554190	HUVEC	blood vessel:	n/a	n/a
33	CTCF	chr11:74554015-74554199	GM19238	blood:	n/a	n/a
34	CTCF	chr11:74554057-74554167	Gliobla	brain:	n/a	n/a
35	CTCF	chr11:74553968-74554168	GM12878	blood:	n/a	n/a
36	CTCF	chr11:74554023-74554215	GM19240	blood:	n/a	n/a
37	CTCF	chr11:74554060-74554210	HRE	kidney:	n/a	n/a
38	CTCF	chr11:74557960-74558110	AG04450	lung:	n/a	n/a
39	CTCF	chr11:74554020-74554170	GM12874	blood:	n/a	n/a
40	CTCF	chr11:74554160-74554310	HCT-116	colon:	n/a	n/a
41	CTCF	chr11:74553820-74553970	AG04450	lung:	n/a	n/a
42	CTCF	chr11:74554040-74554190	HVMF	connective:	n/a	n/a
43	CTCF	chr11:74557880-74558030	HMF	breast:	n/a	n/a
44	CTCF	chr11:74557940-74558090	AG10803	skin:	n/a	n/a
45	CTCF	chr11:74554062-74554185	HUVEC	blood vessel:	n/a	n/a
46	CTCF	chr11:74554082-74554154	HepG2	liver:	n/a	n/a
47	CTCF	chr11:74554100-74554250	MCF-7	breast:	n/a	n/a
48	CTCF	chr11:74554116-74554136	ProgFib	skin:	n/a	n/a
49	CTCF	chr11:74557960-74558110	HUVEC	blood vessel:	n/a	n/a
50	CTCF	chr11:74554000-74554150	GM12871	blood:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:74554171-74554221	HRPEpiC	eye:	n/a
2	chr11:74554171-74554221	GM06990	blood:	n/a
3	chr11:74554171-74554221	A549	lung:	n/a
4	chr11:74554171-74554221	NH-A	brain:	n/a
5	chr11:74554171-74554221	SK-N-SH	brain:	n/a
6	chr11:74554171-74554221	SK-N-MC	brain:	n/a
7	chr11:74554171-74554221	Hepatocyte	liver:	n/a
8	chr11:74554171-74554221	HEK293	kidney:	embryo
9	chr11:74554171-74554221	GM19239	blood:	n/a
10	chr11:74554171-74554221	SK-N-SH_RA	brain:	n/a
11	chr11:74554171-74554221	HIPEpiC	eye:	n/a
12	chr11:74554171-74554221	U87	brain:	n/a
13	chr11:74554171-74554221	HUVEC	blood vessel:	n/a
14	chr11:74554171-74554221	ProgFib	skin:	n/a
15	chr11:74554171-74554221	PrEC	prostate:	n/a
16	chr11:74554171-74554221	HPAEpiC	pulmonary alveolar:	n/a
17	chr11:74554171-74554221	K562	blood:	n/a
18	chr11:74554171-74554221	SKMC	muscle:	n/a
19	chr11:74554171-74554221	PFSK-1	brain:	n/a
20	chr11:74554171-74554221	Caco-2	colon:	n/a
21	chr11:74554171-74554221	HepG2	liver:	n/a
22	chr11:74554171-74554221	BJ	skin:	n/a
23	chr11:74554171-74554221	HEEpiC	esophagus:	n/a
24	chr11:74554171-74554221	Hela-S3	cervix:	n/a
25	chr11:74554171-74554221	NB4	blood:	n/a
26	chr11:74554171-74554221	CMK	blood:	n/a
27	chr11:74554171-74554221	ECC-1	luminal epithelium:	n/a
28	chr11:74554171-74554221	NHBE	bronchial:	n/a
29	chr11:74554171-74554221	AG09319	gingival:	n/a
30	chr11:74554171-74554221	MCF10A-Er-Src	breast:	n/a
31	chr11:74554171-74554221	NHDF-neo	bronchial:	n/a
32	chr11:74554171-74554221	HCPEpiC	choroid plexus:	n/a
33	chr11:74554171-74554221	H1-hESC	embryonic stem cell:	embryo
34	chr11:74554171-74554221	HAEpiC	amniotic membrane:	n/a
35	chr11:74554171-74554221	HCF	heart:	n/a
36	chr11:74554171-74554221	NT2-D1	testis:	n/a
37	chr11:74554171-74554221	T-47D	breast:	n/a
38	chr11:74554171-74554221	GM12878	blood:	n/a
39	chr11:74554171-74554221	ovcar-3	ovarian:	n/a
40	chr11:74554171-74554221	HRE	kidney:	n/a
41	chr11:74554171-74554221	LNCaP	prostate:	n/a
42	chr11:74554171-74554221	HCM	heart:	n/a
43	chr11:74554171-74554221	IMR90	lung:	fetal
44	chr11:74554171-74554221	AG10803	skin:	n/a
45	chr11:74554171-74554221	AoSMC	blood vessel:	n/a
46	chr11:74554171-74554221	SAEC	small airway:	n/a
47	chr11:74554171-74554221	MCF-7	breast:	n/a
48	chr11:74554171-74554221	AG09309	skin:	n/a
49	chr11:74554171-74554221	HMEC	breast:	n/a
50	chr11:74554171-74554221	Jurkat	blood:	n/a

(count:13 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:74551532..74554189-chr11:74554328..74556316,4	K562	blood:
2	chr11:74458806..74461358-chr11:74554734..74556574,2	MCF-7	breast:
3	chr11:74546385..74548948-chr11:74553952..74556769,3	K562	blood:
4	chr11:74547278..74549231-chr11:74557755..74560343,2	K562	blood:
5	chr11:74551532..74554189-chr11:74554328..74556316,4	K562	blood:
6	chr11:74547278..74549879-chr11:74556905..74560343,3	K562	blood:
7	chr11:74547448..74549876-chr11:74553535..74556398,2	K562	blood:
8	chr11:74551815..74554454-chr11:74557454..74559608,2	K562	blood:
9	chr11:74449856..74451588-chr11:74552706..74555219,2	K562	blood:
10	chr11:74550798..74553553-chr11:74554025..74555880,2	MCF-7	breast:
11	chr11:74557579..74558508-chr3:7588338..7588971,2	K562	blood:
12	chr11:74551815..74554454-chr11:74557454..74559608,2	K562	blood:
13	chr11:74552536..74554674-chr11:74560171..74562245,2	K562	blood:

(count:2 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RNF169-2	chr11:74556496-74556696	NONHSAT022959
2	lnc-RNF169-1	chr11:74556955-74557251	NONHSAT022960

No data

Variant related genes	Relation type
RN7SL239P	TF binding region
RN7SL239P	CpG island
ENSG00000166439	chromatin interactions

Extended variants
information (count: 221 )
Associated
traits (count: 102 )

Variant overlapped rSNPs/rCNVs (count:221 , 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	rs563524831	chr11:74553863-74553864	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs533685158	chr11:74553983-74553984	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs147022369	chr11:74553989-74553990	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs370209267	chr11:74553990-74553991	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs374121499	chr11:74554012-74554013	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs377764208	chr11:74554061-74554062	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs552544930	chr11:74554072-74554073	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs561013497	chr11:74554090-74554091	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs517666	chr11:74554147-74554148	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
10	rs536041721	chr11:74554172-74554173	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs368040724	chr11:74554182-74554183	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs554410598	chr11:74554199-74554200	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs370921187	chr11:74554214-74554215	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs568147057	chr11:74554217-74554218	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs374092633	chr11:74554227-74554228	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs202244893	chr11:74554292-74554293	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs576393577	chr11:74554299-74554300	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs534624848	chr11:74554331-74554332	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs370338801	chr11:74554335-74554336	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs374108475	chr11:74554342-74554343	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs539368525	chr11:74554363-74554364	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs186896347	chr11:74554368-74554369	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs372121351	chr11:74554374-74554375	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs374342291	chr11:74554379-74554380	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs368411563	chr11:74554398-74554399	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs148718535	chr11:74554408-74554409	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs149777428	chr11:74554418-74554419	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs562087679	chr11:74554432-74554433	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs375402806	chr11:74554446-74554447	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs200857751	chr11:74554472-74554473	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs200561399	chr11:74554495-74554496	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs564528281	chr11:74554536-74554537	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs533343802	chr11:74554581-74554582	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs550529453	chr11:74554606-74554607	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs693275	chr11:74554672-74554673	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
36	rs558391253	chr11:74554683-74554684	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs529561824	chr11:74554746-74554747	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs549560284	chr11:74554762-74554763	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs568048162	chr11:74554772-74554773	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs533901055	chr11:74554776-74554777	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs150848959	chr11:74554789-74554790	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs570138133	chr11:74554824-74554825	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs539027892	chr11:74554832-74554833	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs76070106	chr11:74554855-74554856	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs75480027	chr11:74554860-74554861	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs199612942	chr11:74554888-74554889	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs374582190	chr11:74554907-74554908	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs555546234	chr11:74554918-74554919	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs113420599	chr11:74554922-74554923	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs199764887	chr11:74554933-74554934	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:102)

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
lymphocytic leukemia	21291569	CNVD
Myelofibrosis	22110671	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Breast cancer	21364760	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
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
Lung cancer	18438408	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Melanoma	20877625	CNVD

Chromatin state (count:320 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:74528000-74576400	Weak transcription	Stomach Mucosa	stomach
2	chr11:74538400-74559000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr11:74538400-74560000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
4	chr11:74538600-74554600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
5	chr11:74539200-74557200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr11:74541800-74556400	Strong transcription	Monocytes-CD14+_RO01746	blood
7	chr11:74543800-74565800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
8	chr11:74544000-74557400	Strong transcription	Dnd41	blood
9	chr11:74544000-74557600	Strong transcription	Primary T helper cells fromperipheralblood	blood
10	chr11:74544200-74557200	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
11	chr11:74544200-74558400	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
12	chr11:74544200-74570800	Strong transcription	Duodenum Mucosa	Duodenum
13	chr11:74545200-74556800	Strong transcription	Primary B cells from peripheral blood	blood
14	chr11:74545600-74564600	Strong transcription	Fetal Muscle Trunk	muscle
15	chr11:74545600-74568400	Strong transcription	Fetal Intestine Large	intestine
16	chr11:74545800-74559800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
17	chr11:74545800-74560400	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
18	chr11:74545800-74565000	Strong transcription	Fetal Muscle Leg	muscle
19	chr11:74546000-74566800	Strong transcription	Fetal Stomach	stomach
20	chr11:74546200-74559400	Strong transcription	Fetal Lung	lung
21	chr11:74547400-74556000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
22	chr11:74547600-74557600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
23	chr11:74547600-74571400	Weak transcription	Fetal Brain Male	brain
24	chr11:74547800-74555200	Weak transcription	H9 Cell Line	embryonic stem cell
25	chr11:74547800-74562800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
26	chr11:74548000-74555400	Weak transcription	Placenta Amnion	Placenta Amnion
27	chr11:74548000-74558200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
28	chr11:74548000-74560600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr11:74548400-74554000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
30	chr11:74548600-74555400	Weak transcription	Small Intestine	intestine
31	chr11:74548800-74560200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
32	chr11:74549400-74567600	Weak transcription	Pancreatic Islets	Pancreatic Islet
33	chr11:74549800-74554000	Weak transcription	Esophagus	oesophagus
34	chr11:74549800-74560400	Weak transcription	Right Atrium	heart
35	chr11:74550600-74557200	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
36	chr11:74550600-74564600	Strong transcription	Fetal Intestine Small	intestine
37	chr11:74550800-74557200	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
38	chr11:74550800-74557400	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
39	chr11:74550800-74557800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
40	chr11:74551000-74554800	Strong transcription	Primary monocytes fromperipheralblood	blood
41	chr11:74551000-74568400	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
42	chr11:74551200-74557400	Strong transcription	Thymus	Thymus
43	chr11:74551200-74557600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
44	chr11:74551200-74559200	Strong transcription	HUES64 Cell Line	embryonic stem cell
45	chr11:74551400-74556800	Strong transcription	Primary neutrophils fromperipheralblood	blood
46	chr11:74551400-74557000	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
47	chr11:74551400-74557800	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr11:74551600-74560200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
49	chr11:74551800-74557400	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
50	chr11:74551800-74557600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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