Variant report

Variant	nsv983187
Chromosome Location	chr11:71815746-71821103
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:54)
CpG islands
(count:122)
Chromatin interactive
region (count:16)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:54 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CTCF	chr11:71818980-71819130	Caco-2	colon:	n/a	n/a
2	CTCF	chr11:71818780-71818930	Caco-2	colon:	n/a	n/a
3	E2F4	chr11:71819421-71819498	MCF10A-Er-Src	breast:	n/a	n/a
4	JUND	chr11:71821038-71821287	HepG2	liver:	n/a	chr11:71821155-71821166
5	MAX	chr11:71819767-71819916	NB4	blood:	n/a	chr11:71819823-71819833
6	MYC	chr11:71817019-71817049	MCF-7	breast:	n/a	n/a
7	POLR2A	chr11:71818398-71821929	H1-hESC	embryonic stem cell:	n/a	n/a
8	POLR2A	chr11:71816952-71817185	GM12878	blood:	n/a	n/a
9	POLR2A	chr11:71812096-71815828	H1-hESC	embryonic stem cell:	n/a	n/a
10	POLR2A	chr11:71817426-71817539	MCF10A-Er-Src	breast:	n/a	n/a
11	POLR2A	chr11:71813300-71815763	GM12878	blood:	n/a	n/a
12	POLR2A	chr11:71819117-71819125	K562	blood:	n/a	n/a
13	POLR2A	chr11:71819347-71819971	H1-hESC	embryonic stem cell:	n/a	n/a
14	POLR2A	chr11:71816895-71817301	H1-hESC	embryonic stem cell:	n/a	n/a
15	POLR2A	chr11:71819133-71819512	HepG2	liver:	n/a	n/a
16	POLR2A	chr11:71819307-71819342	H1-hESC	embryonic stem cell:	n/a	n/a
17	POLR2A	chr11:71816729-71817263	GM12878	blood:	n/a	n/a
18	POLR2A	chr11:71815418-71815902	GM12892	blood:	n/a	n/a
19	POLR2A	chr11:71819612-71819947	H1-hESC	embryonic stem cell:	n/a	n/a
20	POLR2A	chr11:71816998-71817012	Hela-S3	cervix:	n/a	n/a
21	POLR2A	chr11:71817395-71817422	MCF10A-Er-Src	breast:	n/a	n/a
22	POLR2A	chr11:71816869-71817258	H1-hESC	embryonic stem cell:	n/a	n/a
23	POLR2A	chr11:71819640-71819698	HepG2	liver:	n/a	n/a
24	POLR2A	chr11:71816873-71817265	GM12891	blood:	n/a	n/a
25	POLR2A	chr11:71816919-71817296	K562	blood:	n/a	n/a
26	POLR2A	chr11:71818783-71818899	Hela-S3	cervix:	n/a	n/a
27	POLR2A	chr11:71815399-71815804	GM12891	blood:	n/a	n/a
28	POLR2A	chr11:71819487-71819541	H1-hESC	embryonic stem cell:	n/a	n/a
29	POLR2A	chr11:71815726-71816378	GM12892	blood:	n/a	n/a
30	POLR2A	chr11:71819613-71819897	GM12878	blood:	n/a	n/a
31	POLR2A	chr11:71819118-71819162	Hela-S3	cervix:	n/a	n/a
32	POLR2A	chr11:71820352-71820573	H1-hESC	embryonic stem cell:	n/a	n/a
33	POLR2A	chr11:71816775-71817638	GM12892	blood:	n/a	n/a
34	POLR2A	chr11:71816679-71816686	Hela-S3	cervix:	n/a	n/a
35	POLR2A	chr11:71820843-71821480	H1-hESC	embryonic stem cell:	n/a	n/a
36	POLR2A	chr11:71815686-71815813	GM12878	blood:	n/a	n/a
37	POLR2A	chr11:71816809-71817319	GM12892	blood:	n/a	n/a
38	POLR2A	chr11:71819154-71819175	K562	blood:	n/a	n/a
39	POLR2A	chr11:71820975-71821523	GM12878	blood:	n/a	n/a
40	POLR2A	chr11:71819932-71820187	HepG2	liver:	n/a	n/a
41	POLR2A	chr11:71816933-71817201	ECC-1	luminal epithelium:	n/a	n/a
42	POLR2A	chr11:71816898-71817794	H1-hESC	embryonic stem cell:	n/a	n/a
43	POLR2A	chr11:71817025-71817116	MCF-7	breast:	n/a	n/a
44	POLR2A	chr11:71821081-71821655	H1-hESC	embryonic stem cell:	n/a	n/a
45	POLR2A	chr11:71819183-71819378	A549	lung:	n/a	n/a
46	POLR2A	chr11:71815608-71815772	HepG2	liver:	n/a	n/a
47	POLR2A	chr11:71819336-71819979	GM12878	blood:	n/a	n/a
48	POLR2A	chr11:71816113-71816116	HepG2	liver:	n/a	n/a
49	POLR2A	chr11:71820753-71821001	H1-hESC	embryonic stem cell:	n/a	n/a
50	POLR2A	chr11:71818909-71819086	H1-hESC	embryonic stem cell:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:71820069-71820119	Caco-2	colon:	n/a
2	chr11:71820069-71820119	RPTEC	kidney:	n/a
3	chr11:71820069-71820119	HCT-116	colon:	n/a
4	chr11:71820069-71820119	AG04450	lung:	fetal
5	chr11:71817706-71817756	HL-60	blood:	n/a
6	chr11:71817706-71817756	SKMC	muscle:	n/a
7	chr11:71820069-71820119	SK-N-MC	brain:	n/a
8	chr11:71817706-71817756	NH-A	brain:	n/a
9	chr11:71820069-71820119	AG09309	skin:	n/a
10	chr11:71817706-71817756	HCPEpiC	choroid plexus:	n/a
11	chr11:71820069-71820119	PANC-1	pancreas:	n/a
12	chr11:71817706-71817756	BJ	skin:	n/a
13	chr11:71820069-71820119	HAEpiC	amniotic membrane:	n/a
14	chr11:71817706-71817756	HCF	heart:	n/a
15	chr11:71817706-71817756	HCM	heart:	n/a
16	chr11:71820069-71820119	HPAEpiC	pulmonary alveolar:	n/a
17	chr11:71817706-71817756	NT2-D1	testis:	n/a
18	chr11:71817706-71817756	AG04450	lung:	fetal
19	chr11:71817706-71817756	HRCEpiC	kidney:	n/a
20	chr11:71817706-71817756	PFSK-1	brain:	n/a
21	chr11:71817706-71817756	SK-N-SH_RA	brain:	n/a
22	chr11:71820069-71820119	Hepatocyte	liver:	n/a
23	chr11:71820069-71820119	GM12878	blood:	n/a
24	chr11:71817706-71817756	A549	lung:	n/a
25	chr11:71820069-71820119	Hela-S3	cervix:	n/a
26	chr11:71817706-71817756	IMR90	lung:	fetal
27	chr11:71820069-71820119	HIPEpiC	eye:	n/a
28	chr11:71820069-71820119	SK-N-SH	brain:	n/a
29	chr11:71817706-71817756	K562	blood:	n/a
30	chr11:71820069-71820119	NT2-D1	testis:	n/a
31	chr11:71817706-71817756	AG04449	skin:	fetal
32	chr11:71820069-71820119	HMEC	breast:	n/a
33	chr11:71817706-71817756	GM12892	blood:	n/a
34	chr11:71820069-71820119	T-47D	breast:	n/a
35	chr11:71820069-71820119	GM19239	blood:	n/a
36	chr11:71817706-71817756	CMK	blood:	n/a
37	chr11:71817706-71817756	HCT-116	colon:	n/a
38	chr11:71817706-71817756	HUVEC	blood vessel:	n/a
39	chr11:71817706-71817756	H1-hESC	embryonic stem cell:	embryo
40	chr11:71817706-71817756	ProgFib	skin:	n/a
41	chr11:71817706-71817756	U87	brain:	n/a
42	chr11:71820069-71820119	GM12892	blood:	n/a
43	chr11:71817706-71817756	HAEpiC	amniotic membrane:	n/a
44	chr11:71820069-71820119	HCF	heart:	n/a
45	chr11:71817706-71817756	Caco-2	colon:	n/a
46	chr11:71817706-71817756	GM19239	blood:	n/a
47	chr11:71817706-71817756	AG10803	skin:	n/a
48	chr11:71817706-71817756	SK-N-SH	brain:	n/a
49	chr11:71820069-71820119	HUVEC	blood vessel:	n/a
50	chr11:71817706-71817756	HepG2	liver:	n/a

(count:16 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:71747646..71754177-chr11:71811554..71816654,6	K562	blood:
2	chr11:71818013..71820422-chr11:71937441..71939069,2	MCF-7	breast:
3	chr11:71813081..71815809-chr11:72144185..72147079,2	K562	blood:
4	chr11:71812576..71816251-chr11:71934138..71937267,4	MCF-7	breast:
5	chr11:71812032..71815862-chr11:71933743..71937376,6	MCF-7	breast:
6	chr11:71776490..71778244-chr11:71818922..71820939,2	K562	blood:
7	chr11:71747688..71754289-chr11:71810930..71816696,13	MCF-7	breast:
8	chr11:71749172..71754555-chr11:71820034..71825981,11	MCF-7	breast:
9	chr11:71749829..71754834-chr11:71810770..71817366,12	MCF-7	breast:
10	chr11:71749313..71752204-chr11:71820647..71824475,4	MCF-7	breast:
11	chr11:71815942..71818522-chr11:71943866..71946809,2	K562	blood:
12	chr11:71817017..71818819-chr21:44311746..44313583,2	MCF-7	breast:
13	chr11:71785228..71787709-chr11:71818324..71820591,2	K562	blood:
14	chr11:71817497..71819718-chr11:71852568..71855106,2	MCF-7	breast:
15	chr11:71751619..71754177-chr11:71813642..71816501,2	K562	blood:
16	chr11:71820588..71822402-chr11:71934430..71936040,2	K562	blood:

No data

Variant related genes	Relation type
FOLR3	TF binding region
LAMTOR1	TF binding region
LRTOMT	TF binding region
FOLR3	CpG island
LAMTOR1	CpG island
LRTOMT	CpG island
ENSG00000165458	chromatin interactions
ENSG00000137497	chromatin interactions
ENSG00000160194	chromatin interactions
ENSG00000162129	chromatin interactions

Extended variants
information (count: 201 )
Associated
traits (count: 103 )

Variant overlapped rSNPs/rCNVs (count:201 , 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	rs557634324	chr11:71815750-71815751	Enhancers Weak transcription Active TSS Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
2	rs575882712	chr11:71815776-71815777	Enhancers Weak transcription Active TSS Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
3	rs138730365	chr11:71815863-71815864	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs555258551	chr11:71815902-71815903	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs573428716	chr11:71815922-71815923	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs149339793	chr11:71815942-71815943	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs144148565	chr11:71815952-71815953	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs80089267	chr11:71815966-71815967	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs544299338	chr11:71815990-71815991	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs562372195	chr11:71816036-71816037	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs12272086	chr11:71816044-71816045	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs548048786	chr11:71816082-71816083	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs12293885	chr11:71816092-71816093	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
14	rs527550364	chr11:71816157-71816158	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs140660363	chr11:71816174-71816175	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs570458900	chr11:71816176-71816177	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs190555615	chr11:71816207-71816208	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs181072062	chr11:71816208-71816209	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs12272213	chr11:71816219-71816220	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
20	rs536871324	chr11:71816226-71816227	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs554816515	chr11:71816234-71816235	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs373334123	chr11:71816270-71816271	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs567165801	chr11:71816272-71816273	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs375860926	chr11:71816362-71816363	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs73543608	chr11:71816373-71816374	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs370465710	chr11:71816374-71816375	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs576807867	chr11:71816465-71816466	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs544334198	chr11:71816468-71816469	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs556254683	chr11:71816472-71816473	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs574566644	chr11:71816475-71816476	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs542012812	chr11:71816518-71816519	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs147411991	chr11:71816535-71816536	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs527630937	chr11:71816599-71816600	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs73543609	chr11:71816619-71816620	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs564102935	chr11:71816733-71816734	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs139296659	chr11:71816745-71816746	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs114895448	chr11:71816766-71816767	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs186049770	chr11:71816767-71816768	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs568162110	chr11:71816836-71816837	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs551430529	chr11:71816871-71816872	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs548805911	chr11:71816881-71816882	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs568074566	chr11:71816944-71816945	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs566951509	chr11:71816946-71816947	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs534538384	chr11:71816965-71816966	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs558808809	chr11:71816993-71816994	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs371708775	chr11:71816999-71817000	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs376459632	chr11:71817058-71817059	ZNF genes & repeats Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs570774925	chr11:71817082-71817083	ZNF genes & repeats Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs537872720	chr11:71817083-71817084	ZNF genes & repeats Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs556093010	chr11:71817087-71817088	ZNF genes & repeats Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 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
Lung cancer	18438408	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
Hodgkin''s lymphoma	17606441	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
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
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
Pancreatic ductal adenocarcinoma	19077451	CNVD
Breast cancer	17142309	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:232 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:71814800-71816400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
2	chr11:71814800-71818600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr11:71814800-71820200	Weak transcription	Aorta	Aorta
4	chr11:71814800-71822600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr11:71815000-71815800	Enhancers	H1 Cell Line	embryonic stem cell
6	chr11:71815000-71815800	Enhancers	Primary neutrophils fromperipheralblood	blood
7	chr11:71815000-71816200	Weak transcription	Fetal Muscle Trunk	muscle
8	chr11:71815000-71816800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
9	chr11:71815000-71817000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr11:71815000-71817000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr11:71815000-71818400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
12	chr11:71815000-71818400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr11:71815000-71818400	Weak transcription	Gastric	stomach
14	chr11:71815000-71818400	Weak transcription	Ovary	ovary
15	chr11:71815000-71818800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
16	chr11:71815000-71819000	Weak transcription	Esophagus	oesophagus
17	chr11:71815000-71820400	Weak transcription	Colonic Mucosa	Colon
18	chr11:71815000-71820800	Weak transcription	H9 Cell Line	embryonic stem cell
19	chr11:71815000-71822200	Weak transcription	HSMMtube	muscle
20	chr11:71815000-71822400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
21	chr11:71815000-71822400	Weak transcription	HMEC	breast
22	chr11:71815000-71822400	Weak transcription	HUVEC	blood vessel
23	chr11:71815000-71822600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
24	chr11:71815000-71822800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr11:71815000-71822800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
26	chr11:71815000-71823000	Weak transcription	Small Intestine	intestine
27	chr11:71815200-71815800	Enhancers	Pancreas	Pancrea
28	chr11:71815200-71815800	Active TSS	Stomach Mucosa	stomach
29	chr11:71815200-71815800	Enhancers	K562	blood
30	chr11:71815200-71816000	Weak transcription	Fetal Brain Female	brain
31	chr11:71815200-71816200	Weak transcription	Primary T cells from cord blood	blood
32	chr11:71815200-71816800	Weak transcription	Brain Germinal Matrix	brain
33	chr11:71815200-71817000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
34	chr11:71815200-71817200	Weak transcription	Fetal Muscle Leg	muscle
35	chr11:71815200-71817200	Strong transcription	NHLF	lung
36	chr11:71815200-71818200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
37	chr11:71815200-71818200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
38	chr11:71815200-71818200	Weak transcription	Fetal Thymus	thymus
39	chr11:71815200-71818400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr11:71815200-71818400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
41	chr11:71815200-71818400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
42	chr11:71815200-71818400	Weak transcription	Brain Inferior Temporal Lobe	brain
43	chr11:71815200-71818400	Weak transcription	Fetal Stomach	stomach
44	chr11:71815200-71818400	Weak transcription	Rectal Mucosa Donor 31	rectum
45	chr11:71815200-71818400	Weak transcription	Thymus	Thymus
46	chr11:71815200-71818400	Weak transcription	NHEK	skin
47	chr11:71815200-71818600	Weak transcription	HUES6 Cell Line	embryonic stem cell
48	chr11:71815200-71818600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
49	chr11:71815200-71818600	Weak transcription	Sigmoid Colon	Sigmoid Colon
50	chr11:71815200-71818800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin

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