Variant report

Variant	nsv541183
Chromosome Location	chr11:120799275-120846585
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1152)
CpG islands
(count:184)
Chromatin interactive
region (count:27)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1152 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:120823578-120823787	HepG2	liver:	n/a	n/a
2	ATF1	chr11:120812662-120812730	K562	blood:	n/a	n/a
3	ATF3	chr11:120800416-120800577	GM12878	blood:	n/a	n/a
4	BACH1	chr11:120804806-120805140	H1-hESC	embryonic stem cell:	n/a	n/a
5	BCL3	chr11:120836019-120836384	GM12878	blood:	n/a	n/a
6	BHLHE40	chr11:120821703-120821916	HepG2	liver:	n/a	chr11:120821771-120821792 chr11:120821775-120821788
7	BHLHE40	chr11:120823265-120823851	GM12878	blood:	n/a	n/a
8	BHLHE40	chr11:120823577-120823830	K562	blood:	n/a	n/a
9	CBX3	chr11:120815777-120816039	K562	blood:	n/a	n/a
10	CBX3	chr11:120815796-120816096	K562	blood:	n/a	n/a
11	CBX3	chr11:120815750-120816255	HCT-116	colon:	n/a	n/a
12	CBX3	chr11:120815734-120816234	HCT-116	colon:	n/a	n/a
13	CEBPB	chr11:120845633-120845651	H1-hESC	embryonic stem cell:	n/a	n/a
14	CEBPB	chr11:120827291-120827397	K562	blood:	n/a	n/a
15	CEBPB	chr11:120815864-120816107	A549	lung:	n/a	n/a
16	CEBPB	chr11:120827244-120827522	IMR90	lung:	n/a	n/a
17	CEBPB	chr11:120827234-120827523	H1-hESC	embryonic stem cell:	n/a	n/a
18	CEBPB	chr11:120815875-120816137	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr11:120827911-120828199	H1-hESC	embryonic stem cell:	n/a	n/a
20	CEBPB	chr11:120815847-120816183	H1-hESC	embryonic stem cell:	n/a	n/a
21	CEBPB	chr11:120827206-120827533	HepG2	liver:	n/a	n/a
22	CHD2	chr11:120823343-120823956	GM12878	blood:	n/a	n/a
23	CHD2	chr11:120823513-120823867	H1-hESC	embryonic stem cell:	n/a	n/a
24	CHD2	chr11:120823547-120823839	HepG2	liver:	n/a	n/a
25	CHD2	chr11:120823546-120823869	Hela-S3	cervix:	n/a	n/a
26	CTCF	chr11:120823529-120823811	A549	lung:	n/a	chr11:120823698-120823719 chr11:120823703-120823721 chr11:120823704-120823720
27	CTCF	chr11:120805220-120805370	GM12867	blood:	n/a	n/a
28	CTCF	chr11:120800440-120800590	HMF	breast:	n/a	chr11:120800523-120800531 chr11:120800519-120800535 chr11:120800520-120800533 chr11:120800518-120800536 chr11:120800513-120800534 chr11:120800520-120800533
29	CTCF	chr11:120815900-120816050	HPAF	blood vessel:	n/a	n/a
30	CTCF	chr11:120799373-120799423	K562	blood:	n/a	chr11:120799386-120799404
31	CTCF	chr11:120815960-120816110	HCT-116	colon:	n/a	n/a
32	CTCF	chr11:120815902-120816043	HepG2	liver:	n/a	n/a
33	CTCF	chr11:120804960-120805110	HPAF	blood vessel:	n/a	n/a
34	CTCF	chr11:120804842-120805125	K562	blood:	n/a	n/a
35	CTCF	chr11:120800480-120800630	MCF-7	breast:	n/a	chr11:120800523-120800531 chr11:120800519-120800535 chr11:120800520-120800533 chr11:120800518-120800536 chr11:120800513-120800534 chr11:120800520-120800533
36	CTCF	chr11:120804940-120805090	HA-sp	spinal cord:	n/a	n/a
37	CTCF	chr11:120804940-120805090	AG09319	gingival:	n/a	n/a
38	CTCF	chr11:120804940-120805090	GM12867	blood:	n/a	n/a
39	CTCF	chr11:120801960-120802110	HRE	kidney:	n/a	n/a
40	CTCF	chr11:120801860-120802010	HPF	lung:	n/a	n/a
41	CTCF	chr11:120801870-120802129	GM19238	blood:	n/a	n/a
42	CTCF	chr11:120800399-120800638	Kidney_OC	kidney:	n/a	chr11:120800523-120800531 chr11:120800519-120800535 chr11:120800520-120800533 chr11:120800518-120800536 chr11:120800513-120800534 chr11:120800520-120800533
43	CTCF	chr11:120823320-120823470	GM12874	blood:	n/a	n/a
44	CTCF	chr11:120815879-120816055	GM19240	blood:	n/a	n/a
45	CTCF	chr11:120800325-120800708	IMR90	lung:	n/a	chr11:120800679-120800692 chr11:120800523-120800531 chr11:120800519-120800535 chr11:120800520-120800533 chr11:120800518-120800536 chr11:120800513-120800534 chr11:120800520-120800533
46	CTCF	chr11:120800480-120800630	HL-60	blood:	n/a	chr11:120800523-120800531 chr11:120800519-120800535 chr11:120800520-120800533 chr11:120800518-120800536 chr11:120800513-120800534 chr11:120800520-120800533
47	CTCF	chr11:120823620-120823770	HepG2	liver:	n/a	chr11:120823698-120823719 chr11:120823703-120823721 chr11:120823704-120823720
48	CTCF	chr11:120804960-120805110	HBMEC	blood vessel:	n/a	n/a
49	CTCF	chr11:120804828-120805176	IMR90	lung:	n/a	n/a
50	CTCF	chr11:120801900-120802050	GM12871	blood:	n/a	n/a

(count:184 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:120827591-120827641	CMK	blood:	n/a
2	chr11:120827591-120827641	CMK	blood:	n/a
3	chr11:120811322-120811372	HMEC	breast:	n/a
4	chr11:120811322-120811372	HepG2	liver:	n/a
5	chr11:120811322-120811372	ovcar-3	ovarian:	n/a
6	chr11:120811322-120811372	NHDF-neo	bronchial:	n/a
7	chr11:120811322-120811372	CMK	blood:	n/a
8	chr11:120827591-120827641	HCF	heart:	n/a
9	chr11:120823575-120823625	NH-A	brain:	n/a
10	chr11:120827591-120827641	ovcar-3	ovarian:	n/a
11	chr11:120827591-120827641	A549	lung:	n/a
12	chr11:120811322-120811372	HIPEpiC	eye:	n/a
13	chr11:120827591-120827641	U87	brain:	n/a
14	chr11:120823575-120823625	A549	lung:	n/a
15	chr11:120827591-120827641	HMEC	breast:	n/a
16	chr11:120827591-120827641	HL-60	blood:	n/a
17	chr11:120827591-120827641	HEK293	kidney:	embryo
18	chr11:120823575-120823625	SKMC	muscle:	n/a
19	chr11:120827591-120827641	HPAEpiC	pulmonary alveolar:	n/a
20	chr11:120823575-120823625	CMK	blood:	n/a
21	chr11:120823575-120823625	NHBE	bronchial:	n/a
22	chr11:120811322-120811372	HCM	heart:	n/a
23	chr11:120823575-120823625	AG09319	gingival:	n/a
24	chr11:120811322-120811372	ProgFib	skin:	n/a
25	chr11:120811322-120811372	GM19239	blood:	n/a
26	chr11:120827591-120827641	T-47D	breast:	n/a
27	chr11:120827591-120827641	Caco-2	colon:	n/a
28	chr11:120811322-120811372	NT2-D1	testis:	n/a
29	chr11:120823575-120823625	LNCaP	prostate:	n/a
30	chr11:120811322-120811372	HEK293	kidney:	embryo
31	chr11:120811322-120811372	HCPEpiC	choroid plexus:	n/a
32	chr11:120827591-120827641	BJ	skin:	n/a
33	chr11:120827591-120827641	PFSK-1	brain:	n/a
34	chr11:120827591-120827641	AG04449	skin:	fetal
35	chr11:120827591-120827641	SK-N-MC	brain:	n/a
36	chr11:120823575-120823625	ovcar-3	ovarian:	n/a
37	chr11:120827591-120827641	ProgFib	skin:	n/a
38	chr11:120811322-120811372	AG10803	skin:	n/a
39	chr11:120811322-120811372	BE2_C	brain:	n/a
40	chr11:120823575-120823625	HAEpiC	amniotic membrane:	n/a
41	chr11:120823575-120823625	AoSMC	blood vessel:	n/a
42	chr11:120811322-120811372	Hepatocyte	liver:	n/a
43	chr11:120811322-120811372	U87	brain:	n/a
44	chr11:120823575-120823625	SK-N-SH_RA	brain:	n/a
45	chr11:120811322-120811372	HL-60	blood:	n/a
46	chr11:120827591-120827641	HepG2	liver:	n/a
47	chr11:120811322-120811372	HEEpiC	esophagus:	n/a
48	chr11:120827591-120827641	MCF10A-Er-Src	breast:	n/a
49	chr11:120827591-120827641	Hela-S3	cervix:	n/a
50	chr11:120827591-120827641	BE2_C	brain:	n/a

(count:27 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:120834004..120836449-chr11:120836974..120839502,2	MCF-7	breast:
2	chr11:120823580..120824185-chr11:120983339..120983938,2	MCF-7	breast:
3	chr11:120834004..120836449-chr11:120836974..120839502,2	MCF-7	breast:
4	chr11:120804961..120805773-chr11:120823455..120824151,4	MCF-7	breast:
5	chr11:120381486..120382067-chr11:120800468..120801115,2	MCF-7	breast:
6	chr11:120536730..120537365-chr11:120823323..120824097,2	K562	blood:
7	chr11:120804744..120805510-chr11:121065438..121066046,3	K562	blood:
8	chr11:120792557..120795244-chr11:120797109..120800513,3	K562	blood:
9	chr11:120381831..120383470-chr11:120823410..120824152,9	MCF-7	breast:
10	chr11:120381525..120382311-chr11:120800501..120801091,2	MCF-7	breast:
11	chr11:120810051..120813045-chr11:120813067..120814965,2	MCF-7	breast:
12	chr11:120804961..120805773-chr11:120823455..120824151,4	MCF-7	breast:
13	chr11:120627392..120628392-chr11:120800177..120801006,5	MCF-7	breast:
14	chr11:120381495..120382199-chr11:120823435..120824077,2	MCF-7	breast:
15	chr11:120492939..120493692-chr11:120823234..120824125,2	MCF-7	breast:
16	chr11:120627379..120628331-chr11:120823222..120824224,4	MCF-7	breast:
17	chr11:120381855..120382546-chr11:120799370..120799895,2	MCF-7	breast:
18	chr11:120629321..120630296-chr11:120800283..120801141,2	MCF-7	breast:
19	chr11:120800360..120800872-chr12:65990289..65990808,2	MCF-7	breast:
20	chr11:120810051..120813045-chr11:120813067..120814965,2	MCF-7	breast:
21	chr11:120381510..120382946-chr11:120823225..120824156,6	K562	blood:
22	chr11:120811157..120812890-chr11:120817282..120819434,3	K562	blood:
23	chr11:120839096..120841129-chr11:120842375..120845130,2	K562	blood:
24	chr11:120839096..120841129-chr11:120842375..120845130,2	K562	blood:
25	chr11:120811157..120812890-chr11:120817282..120819434,3	K562	blood:
26	chr11:120669903..120670453-chr11:120801797..120802326,2	MCF-7	breast:
27	chr11:120685694..120686556-chr11:120823301..120824043,2	K562	blood:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TRIM29-6	chr11:120806811-120807363	NONHSAT024734
2	lnc-TRIM29-8	chr11:120823250-120825818	ucscGeneNc_uc001pxw_1
3	lnc-TRIM29-7	chr11:120811233-120811600	NONHSAT024735
4	lnc-TRIM29-8	chr11:120828594-120828932	ucscGeneNc_uc001pxw_1
5	lnc-TRIM29-7	chr11:120821658-120821746	NONHSAT024735

No data

Variant related genes	Relation type
HMGB1P42	TF binding region
HMGB1P42	CpG island
ENSG00000149403	chromatin interactions
ENSG00000204306	chromatin interactions

Extended variants
information (count: 1804 )
Associated
traits (count: 98 )

Variant overlapped rSNPs/rCNVs (count:1804 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs145262827	chr11:120799308-120799309	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs190383402	chr11:120799309-120799310	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs182730843	chr11:120799340-120799341	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs376466437	chr11:120799369-120799370	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs538512524	chr11:120799376-120799377	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs561617667	chr11:120799377-120799378	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs577047629	chr11:120799386-120799387	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs185592590	chr11:120799502-120799503	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs544441788	chr11:120799504-120799505	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs547148922	chr11:120799523-120799524	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs565857622	chr11:120799533-120799534	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs377343080	chr11:120799553-120799554	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs3020102	chr11:120799619-120799620	Enhancers Genic enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs138623073	chr11:120799670-120799671	Enhancers Genic enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs12098909	chr11:120799681-120799682	Enhancers Genic enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs2852240	chr11:120799689-120799690	Enhancers Genic enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs61901452	chr11:120799693-120799694	Enhancers Genic enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs376995702	chr11:120799695-120799696	Enhancers Genic enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs113640703	chr11:120799697-120799698	Enhancers Genic enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs2852239	chr11:120799701-120799702	Enhancers Genic enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs537016376	chr11:120799709-120799710	Enhancers Genic enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs544483590	chr11:120799715-120799716	Enhancers Genic enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs546719282	chr11:120799731-120799732	Enhancers Genic enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs72400411	chr11:120799732-120799733	Enhancers Genic enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs71050760	chr11:120799736-120799737	Enhancers Genic enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs28460582	chr11:120799744-120799745	Enhancers Genic enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs370947238	chr11:120799746-120799747	Enhancers Genic enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs12099317	chr11:120799750-120799751	Enhancers Genic enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs10892646	chr11:120799752-120799753	Enhancers Genic enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs535327833	chr11:120799775-120799776	Enhancers Genic enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs553438843	chr11:120799795-120799796	Enhancers Genic enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs578109034	chr11:120799830-120799831	Enhancers Genic enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs545309105	chr11:120799872-120799873	Enhancers Genic enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs562496482	chr11:120799910-120799911	Enhancers Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs190646146	chr11:120799923-120799924	Enhancers Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs183254130	chr11:120799943-120799944	Enhancers Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs77543349	chr11:120800017-120800018	Enhancers Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs12225735	chr11:120800039-120800040	Enhancers Genic enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs143078138	chr11:120800044-120800045	Enhancers Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs11606586	chr11:120800052-120800053	Enhancers Genic enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs541885670	chr11:120800075-120800076	Enhancers Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs74755036	chr11:120800130-120800131	Enhancers Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs569688231	chr11:120800163-120800164	Enhancers Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs79439370	chr11:120800164-120800165	Enhancers Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs143471218	chr11:120800204-120800205	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs369542491	chr11:120800206-120800207	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs560133821	chr11:120800217-120800218	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs189214129	chr11:120800271-120800272	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs73007850	chr11:120800291-120800292	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs4936564	chr11:120800376-120800377	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:98)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Wilms tumour	21544195	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Acute myeloid leukemia	20729466	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
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Cervical cancer	21062161	CNVD
Esophageal squamous carcinoma	18350619	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neuroblastoma	18923191	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	22429812	CNVD
Breast cancer	16608533	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
T-cell lymphomas	19863542	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Basal cell lymphoma	17053054	CNVD
Hepatocellular carcinoma	16785998	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21785460	CNVD
Acute myeloid leukemia	21251322	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	21958427	CNVD
Lung cancer	18438408	CNVD
Ewing''s sarcoma	17952124	CNVD
Breast cancer	17133270	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	17603634	CNVD
Breast cancer	21364760	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Ovarian cancer	21720365	CNVD
Neuroblastoma	17327916	CNVD
Malignant melanoma	17260012	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Prostate cancer	16573809	CNVD
Prostate cancer	18632612	CNVD
Renal cell carcinoma	21668985	CNVD
Developmental delay	21147756	CNVD
Squamous cell cancer	20885788	CNVD
Renal cell carcinoma	18765545	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Neurocytoma	17123091	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Central neurocytomas	17123091	CNVD
Congenital diaphragmatic hernia	21525063	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Multiple myeloma	16616336	CNVD
Hepatocellular carcinoma	16750200	CNVD
Multiple myeloma	17550852	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Acute myeloid leukemia	19651601	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Breast cancer	20409316	CNVD
Salivary gland adenoid cystic carcinoma	17545515	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Heart disease	20551144	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Autism	22543975	CNVD
Breast cancer	21509527	CNVD
Barrett''s syndrome	19417022	CNVD
Myelofibrosis	22110671	CNVD
Cancer	21183584	CNVD
Non-small cell lung cancer	21385341	CNVD
Multiple myeloma	16461302	CNVD
Burkitt''s lymphoma	18698080	CNVD
Prostate cancer	23792589	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:460 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:120747400-120799400	Weak transcription	Brain Cingulate Gyrus	brain
2	chr11:120779800-120799800	Weak transcription	Brain Hippocampus Middle	brain
3	chr11:120795000-120799600	Weak transcription	Fetal Brain Male	brain
4	chr11:120796200-120799600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr11:120796400-120799400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
6	chr11:120797000-120800600	Weak transcription	Fetal Lung	lung
7	chr11:120798800-120800200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr11:120799000-120800200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr11:120799200-120800400	Enhancers	ES-I3 Cell Line	embryonic stem cell
10	chr11:120799400-120800400	Enhancers	Brain Cingulate Gyrus	brain
11	chr11:120799400-120800800	Enhancers	Breast Myoepithelial Primary Cells	Breast
12	chr11:120799600-120800200	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr11:120799600-120800200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
14	chr11:120799600-120800400	Enhancers	HSMMtube	muscle
15	chr11:120799600-120800600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
16	chr11:120799600-120800800	Enhancers	Fetal Heart	heart
17	chr11:120799600-120801000	Enhancers	Fetal Brain Male	brain
18	chr11:120799800-120800000	Enhancers	Brain Hippocampus Middle	brain
19	chr11:120799800-120800200	Enhancers	Brain Inferior Temporal Lobe	brain
20	chr11:120799800-120800200	Enhancers	Brain Substantia Nigra	brain
21	chr11:120799800-120800400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
22	chr11:120799800-120800400	Enhancers	Brain Anterior Caudate	brain
23	chr11:120799800-120801000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
24	chr11:120800000-120800400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
25	chr11:120800000-120800400	Weak transcription	Brain Hippocampus Middle	brain
26	chr11:120800000-120800600	Enhancers	Placenta	Placenta
27	chr11:120800000-120800600	Enhancers	Right Atrium	heart
28	chr11:120800000-120800800	Enhancers	H1 Cell Line	embryonic stem cell
29	chr11:120800200-120800400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr11:120800200-120800400	Enhancers	GM12878-XiMat	blood
31	chr11:120800200-120800600	Enhancers	Fetal Muscle Leg	muscle
32	chr11:120800200-120801200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
33	chr11:120800200-120803200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr11:120800200-120805000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
35	chr11:120800200-120805000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
36	chr11:120800200-120808200	Weak transcription	Brain Inferior Temporal Lobe	brain
37	chr11:120800400-120800600	Enhancers	Brain Hippocampus Middle	brain
38	chr11:120800400-120800600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
39	chr11:120800400-120808400	Weak transcription	Brain Anterior Caudate	brain
40	chr11:120800600-120800800	Enhancers	Duodenum Mucosa	Duodenum
41	chr11:120800600-120801000	Enhancers	Fetal Lung	lung
42	chr11:120800600-120802600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr11:120800600-120802600	Weak transcription	Fetal Muscle Leg	muscle
44	chr11:120800600-120815200	Weak transcription	Brain Hippocampus Middle	brain
45	chr11:120800800-120805000	Weak transcription	H1 Cell Line	embryonic stem cell
46	chr11:120801000-120811400	Weak transcription	Fetal Lung	lung
47	chr11:120801200-120801600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
48	chr11:120801600-120802000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
49	chr11:120801800-120802200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
50	chr11:120801800-120802200	Enhancers	Ovary	ovary

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