Variant report

Variant	nsv897206
Chromosome Location	chr11:34253421-34337564
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1708)
CpG islands
(count:672)
Chromatin interactive
region (count:88)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1708 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:34263663-34263838	K562	blood:	n/a	n/a
2	ARID3A	chr11:34330729-34331219	HepG2	liver:	n/a	n/a
3	ARID3A	chr11:34272488-34272500	K562	blood:	n/a	n/a
4	ARID3A	chr11:34258144-34258360	K562	blood:	n/a	n/a
5	ARID3A	chr11:34331458-34331706	HepG2	liver:	n/a	n/a
6	ATF1	chr11:34263622-34264047	K562	blood:	n/a	n/a
7	ATF1	chr11:34271202-34271360	K562	blood:	n/a	n/a
8	ATF1	chr11:34258159-34258470	K562	blood:	n/a	n/a
9	ATF1	chr11:34255636-34255924	K562	blood:	n/a	n/a
10	ATF1	chr11:34264548-34264774	K562	blood:	n/a	n/a
11	ATF2	chr11:34253173-34253663	GM12878	blood:	n/a	n/a
12	ATF2	chr11:34256665-34257227	GM12878	blood:	n/a	n/a
13	ATF2	chr11:34255499-34256159	GM12878	blood:	n/a	n/a
14	ATF2	chr11:34261244-34261828	GM12878	blood:	n/a	n/a
15	ATF2	chr11:34265540-34266147	GM12878	blood:	n/a	n/a
16	ATF2	chr11:34323938-34324575	GM12878	blood:	n/a	n/a
17	ATF2	chr11:34255540-34255940	H1-hESC	embryonic stem cell:	n/a	n/a
18	ATF2	chr11:34263526-34263963	GM12878	blood:	n/a	n/a
19	ATF2	chr11:34255380-34256269	GM12878	blood:	n/a	n/a
20	ATF2	chr11:34265488-34266211	GM12878	blood:	n/a	n/a
21	ATF2	chr11:34256641-34257339	GM12878	blood:	n/a	n/a
22	ATF2	chr11:34324042-34324553	GM12878	blood:	n/a	n/a
23	ATF3	chr11:34264947-34265689	A549	lung:	n/a	n/a
24	ATF3	chr11:34296192-34296750	A549	lung:	n/a	chr11:34296469-34296480 chr11:34296470-34296481 chr11:34296467-34296480 chr11:34296459-34296479 chr11:34296471-34296481 chr11:34296467-34296482 chr11:34296470-34296478 chr11:34296468-34296478 chr11:34296467-34296478 chr11:34296469-34296482 chr11:34296471-34296478 chr11:34296468-34296481
25	BACH1	chr11:34337547-34337584	H1-hESC	embryonic stem cell:	n/a	n/a
26	BACH1	chr11:34265215-34265539	H1-hESC	embryonic stem cell:	n/a	n/a
27	BACH1	chr11:34255562-34255974	H1-hESC	embryonic stem cell:	n/a	n/a
28	BATF	chr11:34256722-34257234	GM12878	blood:	n/a	n/a
29	BATF	chr11:34261472-34261820	GM12878	blood:	n/a	n/a
30	BATF	chr11:34265565-34266061	GM12878	blood:	n/a	n/a
31	BATF	chr11:34255571-34256220	GM12878	blood:	n/a	n/a
32	BATF	chr11:34323976-34324512	GM12878	blood:	n/a	chr11:34324172-34324182
33	BATF	chr11:34324025-34324515	GM12878	blood:	n/a	chr11:34324172-34324182
34	BATF	chr11:34265298-34266102	GM12878	blood:	n/a	n/a
35	BATF	chr11:34256617-34257256	GM12878	blood:	n/a	n/a
36	BATF	chr11:34253222-34253532	GM12878	blood:	n/a	n/a
37	BATF	chr11:34270025-34270281	GM12878	blood:	n/a	n/a
38	BCL11A	chr11:34256644-34257202	GM12878	blood:	n/a	n/a
39	BCL11A	chr11:34261392-34261842	GM12878	blood:	n/a	chr11:34261556-34261565
40	BCL11A	chr11:34269963-34270339	GM12878	blood:	n/a	n/a
41	BCL11A	chr11:34255701-34256085	GM12878	blood:	n/a	chr11:34255960-34255969 chr11:34255961-34255970
42	BCL11A	chr11:34253175-34253472	GM12878	blood:	n/a	n/a
43	BCL11A	chr11:34265602-34266021	GM12878	blood:	n/a	n/a
44	BCL11A	chr11:34255514-34256163	GM12878	blood:	n/a	chr11:34255960-34255969 chr11:34255961-34255970 chr11:34255679-34255688
45	BCL11A	chr11:34324010-34324466	GM12878	blood:	n/a	chr11:34324174-34324183 chr11:34324175-34324184
46	BCL11A	chr11:34269972-34270387	GM12878	blood:	n/a	n/a
47	BCL11A	chr11:34256783-34257188	GM12878	blood:	n/a	n/a
48	BCL11A	chr11:34324042-34324477	GM12878	blood:	n/a	chr11:34324174-34324183 chr11:34324175-34324184
49	BCL11A	chr11:34265561-34266037	GM12878	blood:	n/a	n/a
50	BCL3	chr11:34255404-34256085	A549	lung:	n/a	chr11:34255960-34255969 chr11:34255961-34255970 chr11:34255679-34255688

(count:672 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:34265361-34265411	HRPEpiC	eye:	n/a
2	chr11:34265361-34265411	HRPEpiC	eye:	n/a
3	chr11:34323678-34323728	BE2_C	brain:	n/a
4	chr11:34322226-34322276	U87	brain:	n/a
5	chr11:34296462-34296512	GM19239	blood:	n/a
6	chr11:34296462-34296512	NT2-D1	testis:	n/a
7	chr11:34255733-34255783	HCPEpiC	choroid plexus:	n/a
8	chr11:34296462-34296512	Hepatocyte	liver:	n/a
9	chr11:34273111-34273161	AG10803	skin:	n/a
10	chr11:34323678-34323728	PrEC	prostate:	n/a
11	chr11:34265361-34265411	NHDF-neo	bronchial:	n/a
12	chr11:34331908-34331958	U87	brain:	n/a
13	chr11:34255733-34255783	HUVEC	blood vessel:	n/a
14	chr11:34256703-34256753	LNCaP	prostate:	n/a
15	chr11:34322226-34322276	SK-N-SH	brain:	n/a
16	chr11:34296462-34296512	HCT-116	colon:	n/a
17	chr11:34296462-34296512	Jurkat	blood:	n/a
18	chr11:34256703-34256753	HNPCEpiC	eye:	n/a
19	chr11:34285529-34285579	T-47D	breast:	n/a
20	chr11:34256703-34256753	HEK293	kidney:	embryo
21	chr11:34273111-34273161	K562	blood:	n/a
22	chr11:34331908-34331958	HCPEpiC	choroid plexus:	n/a
23	chr11:34288225-34288275	HRCEpiC	kidney:	n/a
24	chr11:34323678-34323728	AG04449	skin:	fetal
25	chr11:34285529-34285579	HCF	heart:	n/a
26	chr11:34285529-34285579	HepG2	liver:	n/a
27	chr11:34255733-34255783	A549	lung:	n/a
28	chr11:34296462-34296512	HCM	heart:	n/a
29	chr11:34256703-34256753	HCT-116	colon:	n/a
30	chr11:34331908-34331958	HCF	heart:	n/a
31	chr11:34265361-34265411	HEK293	kidney:	embryo
32	chr11:34273111-34273161	HCT-116	colon:	n/a
33	chr11:34288225-34288275	Hepatocyte	liver:	n/a
34	chr11:34255733-34255783	HEK293	kidney:	embryo
35	chr11:34273111-34273161	GM12878	blood:	n/a
36	chr11:34323678-34323728	HL-60	blood:	n/a
37	chr11:34273111-34273161	HCM	heart:	n/a
38	chr11:34255733-34255783	NT2-D1	testis:	n/a
39	chr11:34255733-34255783	NHDF-neo	bronchial:	n/a
40	chr11:34256703-34256753	HRPEpiC	eye:	n/a
41	chr11:34265361-34265411	Caco-2	colon:	n/a
42	chr11:34285529-34285579	SK-N-SH	brain:	n/a
43	chr11:34255733-34255783	RPTEC	kidney:	n/a
44	chr11:34331908-34331958	AG09319	gingival:	n/a
45	chr11:34288225-34288275	SKMC	muscle:	n/a
46	chr11:34285529-34285579	NT2-D1	testis:	n/a
47	chr11:34256703-34256753	SKMC	muscle:	n/a
48	chr11:34296462-34296512	LNCaP	prostate:	n/a
49	chr11:34296462-34296512	HUVEC	blood vessel:	n/a
50	chr11:34323678-34323728	HCM	heart:	n/a

(count:88 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr11:34229883..34232389-chr11:34271160..34273308,2	K562	blood:
2	chr11:34306120..34306999-chr11:34317675..34318487,2	MCF-7	breast:
3	chr11:34267721..34270365-chr11:34272865..34274585,2	MCF-7	breast:
4	chr11:34224045..34226285-chr11:34321256..34323357,2	MCF-7	breast:
5	chr11:34269717..34273624-chr11:34376687..34380089,5	MCF-7	breast:
6	chr11:34261414..34263986-chr11:34271757..34273793,2	K562	blood:
7	chr11:34295678..34297424-chr11:34350802..34352838,2	MCF-7	breast:
8	chr11:34331497..34333782-chr11:34370435..34371982,2	MCF-7	breast:
9	chr11:34264193..34265705-chr11:34292865..34295828,2	K562	blood:
10	chr11:34285128..34287533-chr11:34298437..34301296,2	MCF-7	breast:
11	chr11:34317934..34320439-chr11:34320796..34323680,2	MCF-7	breast:
12	chr11:34303207..34305928-chr11:34378915..34380855,2	MCF-7	breast:
13	chr11:34330140..34331933-chr11:34345300..34347720,2	K562	blood:
14	chr11:34285128..34287533-chr11:34298437..34301296,2	MCF-7	breast:
15	chr11:34295969..34298454-chr11:34328816..34331408,3	MCF-7	breast:
16	chr11:34306498..34309319-chr11:34324159..34326964,2	MCF-7	breast:
17	chr11:34229441..34231710-chr11:34255472..34258756,3	MCF-7	breast:
18	chr11:34295781..34298473-chr11:34301568..34303802,2	MCF-7	breast:
19	chr11:34256033..34257760-chr11:34260641..34262431,2	K562	blood:
20	chr11:34310476..34312267-chr11:34326192..34328969,2	MCF-7	breast:
21	chr11:34256033..34257760-chr11:34260641..34262431,2	K562	blood:
22	chr11:34295048..34297358-chr11:34352691..34354542,2	MCF-7	breast:
23	chr11:34270206..34274230-chr11:34378598..34380931,3	MCF-7	breast:
24	chr11:34276940..34279788-chr11:34309195..34311703,2	MCF-7	breast:
25	chr11:34278645..34281276-chr11:34285188..34287550,2	K562	blood:
26	chr11:34267721..34270365-chr11:34272865..34274585,2	MCF-7	breast:
27	chr11:34329413..34331132-chr11:34333216..34335602,2	K562	blood:
28	chr11:34281972..34284178-chr11:34286435..34290431,3	K562	blood:
29	chr11:34295969..34298454-chr11:34328816..34331408,3	MCF-7	breast:
30	chr11:34295781..34298473-chr11:34301568..34303802,2	MCF-7	breast:
31	chr11:34254769..34257518-chr11:34263900..34266853,2	K562	blood:
32	chr11:34336235..34339899-chr11:34377222..34380179,3	MCF-7	breast:
33	chr11:34297526..34299830-chr11:34304007..34305753,2	MCF-7	breast:
34	chr11:34316702..34320022-chr11:34376124..34379659,5	MCF-7	breast:
35	chr11:34308939..34311768-chr11:34379486..34381875,2	MCF-7	breast:
36	chr11:34227777..34229302-chr11:34277584..34279441,2	MCF-7	breast:
37	chr11:34323353..34325328-chr11:34327561..34330383,2	MCF-7	breast:
38	chr11:34283475..34285529-chr11:34358260..34360841,2	MCF-7	breast:
39	chr11:34323353..34325328-chr11:34327561..34330383,2	MCF-7	breast:
40	chr11:34309410..34312078-chr11:34318122..34319816,2	K562	blood:
41	chr11:34244635..34246968-chr11:34254432..34256180,2	K562	blood:
42	chr11:34256786..34259420-chr11:34262602..34265053,3	K562	blood:
43	chr11:34264193..34265705-chr11:34292865..34295828,2	K562	blood:
44	chr11:34295302..34298402-chr11:34377411..34380929,7	MCF-7	breast:
45	chr11:34284799..34287708-chr11:34289917..34291890,2	K562	blood:
46	chr11:34261414..34263986-chr11:34271757..34273793,2	K562	blood:
47	chr11:34328956..34331154-chr11:34336268..34338352,2	K562	blood:
48	chr11:34297526..34299830-chr11:34304007..34305753,2	MCF-7	breast:
49	chr11:34306120..34306643-chr11:34317612..34318175,2	MCF-7	breast:
50	chr11:34265214..34267176-chr11:34283077..34285328,3	MCF-7	breast:

No data

Variant related genes	Relation type
ABTB2	TF binding region
ABTB2	CpG island
ENSG00000135372	chromatin interactions
ENSG00000166016	chromatin interactions

Extended variants
information (count: 3334 )
Associated
traits (count: 80 )

Variant overlapped rSNPs/rCNVs (count:3334 , 50 per page) page: 1 2 3 4 5 6 7 ... 67

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4756118	chr11:34253421-34253422	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs189949243	chr11:34253430-34253431	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs182371725	chr11:34253519-34253520	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs117035739	chr11:34253549-34253550	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs114602771	chr11:34253680-34253681	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs2926467	chr11:34253683-34253684	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
7	rs78475148	chr11:34253774-34253775	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs576195378	chr11:34253790-34253791	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs571036772	chr11:34253810-34253811	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs186322500	chr11:34253869-34253870	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs558937006	chr11:34253870-34253871	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs2955952	chr11:34253879-34253880	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs541052437	chr11:34253904-34253905	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs561363290	chr11:34253929-34253930	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs2955951	chr11:34253951-34253952	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs543903063	chr11:34253954-34253955	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs368170125	chr11:34253961-34253962	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs563785129	chr11:34253972-34253973	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs192327272	chr11:34253973-34253974	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs370512516	chr11:34253996-34253997	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs67998044	chr11:34253997-34253998	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs2957511	chr11:34254007-34254008	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs397834843	chr11:34254013-34254014	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs2955950	chr11:34254014-34254015	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs527615676	chr11:34254031-34254032	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs17255930	chr11:34254039-34254040	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs114650617	chr11:34254073-34254074	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs2955949	chr11:34254075-34254076	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
29	rs57295752	chr11:34254108-34254109	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs2955948	chr11:34254160-34254161	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs569415805	chr11:34254170-34254171	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs538854834	chr11:34254181-34254182	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs559141320	chr11:34254204-34254205	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs572630437	chr11:34254228-34254229	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs374588278	chr11:34254233-34254234	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs7106936	chr11:34254249-34254250	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs555318467	chr11:34254302-34254303	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs200858367	chr11:34254342-34254343	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs2467371	chr11:34254404-34254405	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs543843391	chr11:34254418-34254419	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs563772289	chr11:34254513-34254514	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs532682316	chr11:34254521-34254522	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs35457013	chr11:34254524-34254525	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs150886641	chr11:34254529-34254530	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs139410014	chr11:34254547-34254548	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs113790603	chr11:34254565-34254566	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs547633958	chr11:34254576-34254577	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs1983756	chr11:34254625-34254626	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs529137093	chr11:34254674-34254675	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs369652453	chr11:34254676-34254677	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:80)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Medulloblastoma	21979893	CNVD
Thyroid cancer	19087340	CNVD
Melanoma	18172304	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Wilms tumour	21544195	CNVD
Parathyroid adenoma	22454399	CNVD
Chordoma	21602918	CNVD
Breast cancer	21949216	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	19222835	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Beckwith-Wiedemann syndrome	21518781	CNVD
Wilms tumour	21518781	CNVD
Hepatoblastoma	21518781	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Gastric cancer	17908304	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Multiple myeloma	20724749	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Autism	22495311	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	21785460	CNVD
Medulloblastoma	16783165	CNVD
small cell lung cancer	20016488	CNVD
Renal cell carcinoma	18194544	CNVD
Potocki-Shaffer syndrome	19222835	CNVD
WAGR syndrome	19222835	CNVD
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Glioblastoma multiforme	22286061	CNVD
Breast cancer	21364760	CNVD
Aniridia syndrome	21572526	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16272173	CNVD
Retinoblastoma	22278416	CNVD
Denys-drash syndrome	21085971	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
WAGR syndrome	16773131	CNVD
Disorders of sex development	22290220	CNVD
Aniridia syndrome	17204608	CNVD
Mental retardation	17204608	CNVD
WAGR syndrome	19617690	CNVD
genitourinary abnormalities	17204608	CNVD
Breast cancer	16397240	CNVD
Mental retardation	16773131	CNVD
Multiple myeloma	16616336	CNVD
Cancer	17160897	CNVD
Cancer	21183584	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
WAGR syndrome	22470819	CNVD
Neurodevelopmental disorder	22521361	CNVD
Denys-drash syndrome	19566914	CNVD
Familial wilms tumor	19566914	CNVD
Frasier syndrome	19566914	CNVD
Non-small cell lung cancer	21829676	CNVD
WAGR syndrome	20603712	CNVD
Autism	17322880	CNVD
Renal cell carcinoma	18765545	CNVD
Breast cancer	21858162	CNVD
Cancer	20164920	CNVD
Breast cancer	16620391	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Cancer	20164919	CNVD

Chromatin state (count:2367 , 50 per page) page: 1 2 3 4 5 6 7 ... 48

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:34237200-34255600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
2	chr11:34245200-34254600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
3	chr11:34245200-34255400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr11:34245200-34255600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr11:34245200-34255800	Weak transcription	HSMMtube	muscle
6	chr11:34245200-34263800	Weak transcription	Right Atrium	heart
7	chr11:34245200-34264200	Weak transcription	Aorta	Aorta
8	chr11:34245400-34254600	Weak transcription	HUES6 Cell Line	embryonic stem cell
9	chr11:34245400-34255600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
10	chr11:34245400-34255600	Weak transcription	NHLF	lung
11	chr11:34245600-34263600	Weak transcription	Right Ventricle	heart
12	chr11:34246200-34255600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr11:34246800-34255800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
14	chr11:34247000-34254800	Weak transcription	Fetal Intestine Small	intestine
15	chr11:34247000-34255800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
16	chr11:34247000-34257400	Weak transcription	Fetal Stomach	stomach
17	chr11:34248200-34254600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
18	chr11:34249600-34263600	Weak transcription	Gastric	stomach
19	chr11:34251600-34255400	Enhancers	GM12878-XiMat	blood
20	chr11:34251800-34255400	Weak transcription	H1 Cell Line	embryonic stem cell
21	chr11:34251800-34255600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
22	chr11:34252000-34255400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
23	chr11:34252000-34255600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
24	chr11:34252600-34253800	Enhancers	A549	lung
25	chr11:34253200-34253600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
26	chr11:34253600-34256000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
27	chr11:34253800-34254600	Weak transcription	A549	lung
28	chr11:34254000-34256400	Enhancers	Primary B cells from peripheral blood	blood
29	chr11:34254200-34255800	Enhancers	iPS-20b Cell Line	embryonic stem cell
30	chr11:34254400-34254600	Weak transcription	Brain Substantia Nigra	brain
31	chr11:34254400-34256200	Enhancers	Primary B cells from cord blood	blood
32	chr11:34254600-34254800	Enhancers	Brain Substantia Nigra	brain
33	chr11:34254600-34255400	Enhancers	HUES6 Cell Line	embryonic stem cell
34	chr11:34254600-34255400	Enhancers	A549	lung
35	chr11:34254600-34256200	Enhancers	HepG2	liver
36	chr11:34254600-34256400	Enhancers	Primary hematopoietic stem cells short term culture	blood
37	chr11:34254600-34258800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
38	chr11:34254800-34255600	Enhancers	Hela-S3	cervix
39	chr11:34254800-34256400	Enhancers	Fetal Intestine Small	intestine
40	chr11:34254800-34257200	Weak transcription	Brain Substantia Nigra	brain
41	chr11:34254800-34257600	Enhancers	Primary T helper cells PMA-I stimulated	--
42	chr11:34255000-34257600	Enhancers	Fetal Thymus	thymus
43	chr11:34255400-34255600	Enhancers	Duodenum Mucosa	Duodenum
44	chr11:34255400-34255600	Enhancers	Rectal Mucosa Donor 31	rectum
45	chr11:34255400-34255600	Bivalent Enhancer	K562	blood
46	chr11:34255400-34255600	Enhancers	NH-A	brain
47	chr11:34255400-34255800	Enhancers	ES-I3 Cell Line	embryonic stem cell
48	chr11:34255400-34255800	Enhancers	HUES48 Cell Line	embryonic stem cell
49	chr11:34255400-34255800	Enhancers	HUES64 Cell Line	embryonic stem cell
50	chr11:34255400-34255800	Enhancers	iPS-18 Cell Line	embryonic stem cell

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