Variant report

Variant	nsv518659
Chromosome Location	chr11:72934619-72946020
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:138)
CpG islands
(count:244)
Chromatin interactive
region (count:36)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:138 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:72944921-72945053	HepG2	liver:	n/a	n/a
2	CTCF	chr11:72938940-72939090	HMEC	breast:	n/a	n/a
3	CTCF	chr11:72938716-72939232	MCF-7	breast:	n/a	chr11:72938912-72938930 chr11:72938914-72938927
4	CTCF	chr11:72938872-72939206	K562	blood:	n/a	chr11:72938912-72938930 chr11:72938914-72938927
5	CTCF	chr11:72939002-72939069	K562	blood:	n/a	n/a
6	CTCF	chr11:72943255-72943314	GM20000	blood:	n/a	n/a
7	CTCF	chr11:72938938-72939140	LNCaP	prostate:	n/a	n/a
8	CTCF	chr11:72938935-72939136	MCF-7	breast:	n/a	n/a
9	CTCF	chr11:72938960-72939110	HRPEpiC	eye:	n/a	n/a
10	CTCF	chr11:72938940-72939090	MCF-7	breast:	n/a	n/a
11	CTCF	chr11:72938960-72939110	WERI-Rb-1	eye:	n/a	n/a
12	CTCF	chr11:72936160-72936310	Caco-2	colon:	n/a	n/a
13	CTCF	chr11:72938980-72939130	SAEC	small airway:	n/a	n/a
14	CTCF	chr11:72938996-72939137	LNCaP	prostate:	n/a	n/a
15	CTCF	chr11:72938920-72939070	SAEC	small airway:	n/a	n/a
16	CTCF	chr11:72938880-72939030	HepG2	liver:	n/a	chr11:72938912-72938930 chr11:72938914-72938927
17	CTCF	chr11:72938960-72939168	Pancreas_OC	pancreas:	n/a	n/a
18	CTCF	chr11:72938960-72939110	HCT-116	colon:	n/a	n/a
19	CTCF	chr11:72938540-72938690	HCT-116	colon:	n/a	n/a
20	CTCF	chr11:72938980-72939130	Caco-2	colon:	n/a	n/a
21	CTCF	chr11:72938960-72939110	MCF-7	breast:	n/a	n/a
22	CTCF	chr11:72938960-72939110	K562	blood:	n/a	n/a
23	CTCF	chr11:72938924-72939148	MCF-7	breast:	n/a	n/a
24	CTCF	chr11:72938894-72939141	H1-hESC	embryonic stem cell:	n/a	chr11:72938912-72938930 chr11:72938914-72938927
25	CTCF	chr11:72938880-72939030	GM12866	blood:	n/a	chr11:72938912-72938930 chr11:72938914-72938927
26	CTCF	chr11:72938920-72939070	Hela-S3	cervix:	n/a	n/a
27	CTCF	chr11:72938980-72939130	HEEpiC	esophagus:	n/a	n/a
28	CTCF	chr11:72938748-72939230	MCF-7	breast:	n/a	chr11:72938912-72938930 chr11:72938914-72938927
29	CTCF	chr11:72938905-72939158	NHEK	skin:	n/a	chr11:72938912-72938930 chr11:72938914-72938927
30	CTCF	chr11:72938960-72939110	GM12864	blood:	n/a	n/a
31	CTCF	chr11:72938960-72939110	Caco-2	colon:	n/a	n/a
32	CTCF	chr11:72939020-72939061	HepG2	liver:	n/a	n/a
33	CTCF	chr11:72938923-72939154	MCF-7	breast:	n/a	n/a
34	CTCF	chr11:72938860-72939129	T-47D	breast:	n/a	chr11:72938912-72938930 chr11:72938914-72938927
35	CTCF	chr11:72938910-72939158	MCF-7	breast:	n/a	chr11:72938912-72938930 chr11:72938914-72938927
36	CTCF	chr11:72938900-72939050	HEK293	kidney:	n/a	chr11:72938912-72938930 chr11:72938914-72938927
37	CTCF	chr11:72938840-72938990	NHEK	skin:	n/a	chr11:72938912-72938930 chr11:72938914-72938927
38	CTCF	chr11:72938829-72939218	H1-hESC	embryonic stem cell:	n/a	chr11:72938912-72938930 chr11:72938914-72938927
39	CTCF	chr11:72939020-72939170	HMEC	breast:	n/a	n/a
40	CTCF	chr11:72939820-72939970	A549	lung:	n/a	n/a
41	CTCF	chr11:72938813-72939254	H1-hESC	embryonic stem cell:	n/a	chr11:72938912-72938930 chr11:72938914-72938927
42	CTCF	chr11:72938920-72939070	NHEK	skin:	n/a	n/a
43	CTCF	chr11:72938925-72939148	MCF-7	breast:	n/a	n/a
44	ELF1	chr11:72938775-72939370	MCF-7	breast:	n/a	chr11:72939103-72939114
45	EP300	chr11:72938786-72939377	T-47D	breast:	n/a	chr11:72939259-72939275
46	EP300	chr11:72938837-72939302	T-47D	breast:	n/a	chr11:72939259-72939275
47	EP300	chr11:72938642-72939542	ECC-1	luminal epithelium:	n/a	chr11:72939259-72939275
48	EP300	chr11:72938868-72939432	ECC-1	luminal epithelium:	n/a	chr11:72939259-72939275
49	EP300	chr11:72938604-72939586	MCF-7	breast:	n/a	chr11:72939259-72939275
50	EP300	chr11:72938682-72939422	MCF-7	breast:	n/a	chr11:72939259-72939275

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:72939150-72939200	SK-N-SH_RA	brain:	n/a
2	chr11:72941691-72941741	HEK293	kidney:	embryo
3	chr11:72943745-72943795	HCF	heart:	n/a
4	chr11:72941203-72941253	HCT-116	colon:	n/a
5	chr11:72939150-72939200	HCF	heart:	n/a
6	chr11:72943745-72943795	HCT-116	colon:	n/a
7	chr11:72941691-72941741	MCF-7	breast:	n/a
8	chr11:72943745-72943795	Jurkat	blood:	n/a
9	chr11:72941691-72941741	MCF10A-Er-Src	breast:	n/a
10	chr11:72941691-72941741	ProgFib	skin:	n/a
11	chr11:72941203-72941253	K562	blood:	n/a
12	chr11:72941691-72941741	AG10803	skin:	n/a
13	chr11:72939150-72939200	NB4	blood:	n/a
14	chr11:72943745-72943795	HEEpiC	esophagus:	n/a
15	chr11:72943745-72943795	SK-N-MC	brain:	n/a
16	chr11:72941203-72941253	NT2-D1	testis:	n/a
17	chr11:72941203-72941253	GM12891	blood:	n/a
18	chr11:72939150-72939200	HCPEpiC	choroid plexus:	n/a
19	chr11:72941691-72941741	HPAEpiC	pulmonary alveolar:	n/a
20	chr11:72941691-72941741	SK-N-SH_RA	brain:	n/a
21	chr11:72943745-72943795	PrEC	prostate:	n/a
22	chr11:72941203-72941253	HUVEC	blood vessel:	n/a
23	chr11:72941203-72941253	BE2_C	brain:	n/a
24	chr11:72939150-72939200	Hela-S3	cervix:	n/a
25	chr11:72943745-72943795	BE2_C	brain:	n/a
26	chr11:72941691-72941741	GM06990	blood:	n/a
27	chr11:72943745-72943795	AG09309	skin:	n/a
28	chr11:72941691-72941741	H1-hESC	embryonic stem cell:	embryo
29	chr11:72941691-72941741	HL-60	blood:	n/a
30	chr11:72943745-72943795	GM19239	blood:	n/a
31	chr11:72941203-72941253	HIPEpiC	eye:	n/a
32	chr11:72943745-72943795	HPAEpiC	pulmonary alveolar:	n/a
33	chr11:72939150-72939200	GM19239	blood:	n/a
34	chr11:72939150-72939200	AG04449	skin:	fetal
35	chr11:72943745-72943795	HL-60	blood:	n/a
36	chr11:72939150-72939200	BJ	skin:	n/a
37	chr11:72941691-72941741	RPTEC	kidney:	n/a
38	chr11:72939150-72939200	AG04450	lung:	fetal
39	chr11:72941203-72941253	HCM	heart:	n/a
40	chr11:72941691-72941741	SK-N-MC	brain:	n/a
41	chr11:72941203-72941253	SK-N-SH_RA	brain:	n/a
42	chr11:72943745-72943795	MCF10A-Er-Src	breast:	n/a
43	chr11:72939150-72939200	A549	lung:	n/a
44	chr11:72939150-72939200	HPAEpiC	pulmonary alveolar:	n/a
45	chr11:72941203-72941253	HAEpiC	amniotic membrane:	n/a
46	chr11:72939150-72939200	HRPEpiC	eye:	n/a
47	chr11:72943745-72943795	GM12878	blood:	n/a
48	chr11:72943745-72943795	RPTEC	kidney:	n/a
49	chr11:72941203-72941253	PrEC	prostate:	n/a
50	chr11:72941691-72941741	PANC-1	pancreas:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr11:72941338..72942987-chr11:72945088..72947125,2	K562	blood:
2	chr11:72944570..72946816-chr11:72949673..72951372,2	K562	blood:
3	chr11:72903126..72904098-chr11:72938581..72939787,8	MCF-7	breast:
4	chr11:72916036..72917695-chr11:72937306..72940279,2	MCF-7	breast:
5	chr11:72906296..72906829-chr11:72938715..72939508,2	MCF-7	breast:
6	chr11:72905403..72906458-chr11:72938724..72939450,3	MCF-7	breast:
7	chr11:72938578..72939503-chr11:72947565..72948485,4	MCF-7	breast:
8	chr11:72937927..72942237-chr11:72945067..72953097,14	MCF-7	breast:
9	chr11:72938628..72940531-chr15:99443133..99444962,2	MCF-7	breast:
10	chr11:72911080..72911617-chr11:72938500..72939391,2	MCF-7	breast:
11	chr11:72941338..72942987-chr11:72945088..72947125,2	K562	blood:
12	chr11:72939098..72939947-chr11:72947304..72948116,2	MCF-7	breast:
13	chr11:72904435..72906277-chr11:72938412..72939756,22	MCF-7	breast:
14	chr11:72931397..72935797-chr11:72938459..72941401,4	K562	blood:
15	chr11:72497171..72498123-chr11:72938613..72939618,3	MCF-7	breast:
16	chr11:72523273..72527057-chr11:72937131..72939927,3	MCF-7	breast:
17	chr11:72944490..72946453-chr11:72952891..72955306,2	MCF-7	breast:
18	chr11:72929084..72930131-chr11:72938648..72939423,5	MCF-7	breast:
19	chr11:72936171..72938814-chr11:72941507..72943078,2	K562	blood:
20	chr11:72936171..72938814-chr11:72941507..72943078,2	K562	blood:
21	chr11:72905511..72906504-chr11:72938562..72939418,3	MCF-7	breast:
22	chr11:72943180..72944892-chr11:72951598..72954377,2	K562	blood:
23	chr11:72928784..72929703-chr11:72938662..72939521,3	MCF-7	breast:
24	chr11:72491387..72492889-chr11:72936381..72939114,2	MCF-7	breast:
25	chr11:72938389..72940654-chr11:72953845..72956300,2	MCF-7	breast:
26	chr11:72503643..72506382-chr11:72935261..72937531,2	MCF-7	breast:
27	chr11:72909923..72912508-chr11:72937140..72938650,2	MCF-7	breast:
28	chr11:72931397..72935797-chr11:72938459..72941401,4	K562	blood:
29	chr11:72929288..72929790-chr11:72939005..72939598,2	MCF-7	breast:
30	chr11:72904985..72905918-chr11:72938897..72939566,2	MCF-7	breast:
31	chr11:72551043..72553984-chr11:72939996..72942753,2	MCF-7	breast:
32	chr11:72492441..72494706-chr11:72945606..72948103,2	MCF-7	breast:
33	chr11:72935321..72937353-chr11:73087469..73089491,2	K562	blood:
34	chr11:72935934..72938365-chr11:72952035..72953904,2	K562	blood:
35	chr11:72496738..72498123-chr11:72938613..72939675,6	MCF-7	breast:
36	chr11:72903145..72906277-chr11:72938581..72939821,37	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000260401	TF binding region
ENSG00000260401	CpG island
ENSG00000054967	chromatin interactions
ENSG00000186635	chromatin interactions
ENSG00000214530	chromatin interactions
ENSG00000265064	chromatin interactions
ENSG00000260401	chromatin interactions
ENSG00000168010	chromatin interactions
ENSG00000140443	chromatin interactions
ENSG00000175591	chromatin interactions

Extended variants
information (count: 483 )
Associated
traits (count: 102 )

Variant overlapped rSNPs/rCNVs (count:483 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12364461	chr11:72934619-72934620	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs566711332	chr11:72934640-72934641	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs373738456	chr11:72934645-72934646	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs538567715	chr11:72934653-72934654	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs190066920	chr11:72934654-72934655	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs574651036	chr11:72934670-72934671	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs575216755	chr11:72934682-72934683	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs544225107	chr11:72934702-72934703	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs183048775	chr11:72934710-72934711	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs4944831	chr11:72934728-72934729	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
11	rs115462262	chr11:72934753-72934754	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs556706356	chr11:72934771-72934772	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs560544105	chr11:72934772-72934773	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs187285478	chr11:72934773-72934774	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs545478992	chr11:72934804-72934805	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs546505354	chr11:72934853-72934854	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs7126411	chr11:72934854-72934855	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs563203433	chr11:72934878-72934879	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs2510883	chr11:72934914-72934915	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs573099166	chr11:72935061-72935062	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs550345036	chr11:72935064-72935065	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs149605095	chr11:72935068-72935069	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs73536987	chr11:72935090-72935091	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs546744336	chr11:72935137-72935138	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs566343344	chr11:72935144-72935145	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs373531576	chr11:72935145-72935146	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs538477556	chr11:72935169-72935170	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs34770116	chr11:72935203-72935204	Enhancers Weak transcription Genic enhancers Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs558406396	chr11:72935204-72935205	Enhancers Weak transcription Genic enhancers Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs116144699	chr11:72935205-72935206	Enhancers Weak transcription Genic enhancers Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs193131956	chr11:72935216-72935217	Enhancers Weak transcription Genic enhancers Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs540479978	chr11:72935225-72935226	Enhancers Weak transcription Genic enhancers Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs545041678	chr11:72935239-72935240	Enhancers Weak transcription Genic enhancers Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs554671607	chr11:72935264-72935265	Enhancers Weak transcription Genic enhancers Bivalent Enhancer Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs574850395	chr11:72935275-72935276	Enhancers Weak transcription Genic enhancers Bivalent Enhancer Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs562360395	chr11:72935278-72935279	Enhancers Weak transcription Genic enhancers Bivalent Enhancer Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs540388921	chr11:72935293-72935294	Enhancers Weak transcription Genic enhancers Bivalent Enhancer Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs554276690	chr11:72935308-72935309	Enhancers Weak transcription Genic enhancers Bivalent Enhancer Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs60292618	chr11:72935319-72935320	Enhancers Weak transcription Genic enhancers Bivalent Enhancer Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs184103134	chr11:72935331-72935332	Enhancers Weak transcription Genic enhancers Bivalent Enhancer Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs80176545	chr11:72935368-72935369	Enhancers Weak transcription Genic enhancers Bivalent Enhancer Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs532053068	chr11:72935373-72935374	Enhancers Weak transcription Genic enhancers Bivalent Enhancer Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs369687018	chr11:72935433-72935434	Enhancers Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs148750419	chr11:72935438-72935439	Enhancers Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs142326262	chr11:72935456-72935457	Enhancers Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs150836064	chr11:72935461-72935462	Enhancers Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs188657553	chr11:72935490-72935491	Enhancers Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs73536991	chr11:72935508-72935509	Enhancers Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs192721387	chr11:72935527-72935528	Enhancers Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs139516340	chr11:72935572-72935573	Enhancers Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	3 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
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
Chronic lymphocytic leukemia	22228453	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
Lung cancer	19153074	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:261 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:72930000-72938400	Weak transcription	Gastric	stomach
2	chr11:72930000-72938400	Weak transcription	Pancreas	Pancrea
3	chr11:72930600-72938800	Weak transcription	A549	lung
4	chr11:72930600-72944200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
5	chr11:72931000-72938400	Weak transcription	Rectal Mucosa Donor 29	rectum
6	chr11:72931200-72935800	Enhancers	Right Ventricle	heart
7	chr11:72931200-72938600	Weak transcription	Colonic Mucosa	Colon
8	chr11:72931400-72935200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
9	chr11:72931400-72936000	Enhancers	Dnd41	blood
10	chr11:72932000-72936000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
11	chr11:72932400-72934800	Genic enhancers	Skeletal Muscle Female	skeletal muscle
12	chr11:72932400-72935000	Enhancers	Left Ventricle	heart
13	chr11:72932400-72936200	Weak transcription	Right Atrium	heart
14	chr11:72932600-72936600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr11:72932800-72936200	Genic enhancers	Skeletal Muscle Male	skeletal muscle
16	chr11:72932800-72936600	Genic enhancers	Monocytes-CD14+_RO01746	blood
17	chr11:72932800-72937000	Weak transcription	HMEC	breast
18	chr11:72932800-72937200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
19	chr11:72932800-72937600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
20	chr11:72933000-72938600	Weak transcription	Fetal Intestine Large	intestine
21	chr11:72933600-72935200	Weak transcription	Lung	lung
22	chr11:72933600-72935800	Strong transcription	Esophagus	oesophagus
23	chr11:72933600-72938600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
24	chr11:72933800-72935000	Weak transcription	Psoas Muscle	Psoas
25	chr11:72934200-72936400	Genic enhancers	Primary monocytes fromperipheralblood	blood
26	chr11:72934400-72935800	Enhancers	Primary neutrophils fromperipheralblood	blood
27	chr11:72934400-72936400	Enhancers	Primary hematopoietic stem cells short term culture	blood
28	chr11:72934400-72936400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
29	chr11:72934400-72941600	Enhancers	Placenta	Placenta
30	chr11:72934600-72935400	Strong transcription	Fetal Intestine Small	intestine
31	chr11:72934600-72935800	Genic enhancers	Spleen	Spleen
32	chr11:72934600-72936800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
33	chr11:72934600-72938600	Weak transcription	Duodenum Mucosa	Duodenum
34	chr11:72934600-72941600	Enhancers	Placenta Amnion	Placenta Amnion
35	chr11:72934800-72935400	Enhancers	Fetal Thymus	thymus
36	chr11:72934800-72936200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
37	chr11:72934800-72939800	Enhancers	Skeletal Muscle Female	skeletal muscle
38	chr11:72935000-72936000	Weak transcription	Left Ventricle	heart
39	chr11:72935000-72936200	Enhancers	Primary hematopoietic stem cells	blood
40	chr11:72935000-72936600	Enhancers	Psoas Muscle	Psoas
41	chr11:72935200-72935400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
42	chr11:72935200-72935400	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
43	chr11:72935200-72935600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
44	chr11:72935200-72937200	Enhancers	Lung	lung
45	chr11:72935400-72936000	Weak transcription	Fetal Intestine Small	intestine
46	chr11:72935400-72938600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
47	chr11:72935800-72936200	Weak transcription	Spleen	Spleen
48	chr11:72935800-72936800	Weak transcription	Esophagus	oesophagus
49	chr11:72935800-72936800	Weak transcription	Right Ventricle	heart
50	chr11:72935800-72937200	Enhancers	Fetal Heart	heart

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