Variant report

Variant	nsv528190
Chromosome Location	chr11:58336620-58347765
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1841)
CpG islands
(count:1408)
Chromatin interactive
region (count:39)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1841 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:58344604-58346214	K562	blood:	n/a	n/a
2	ARID3A	chr11:58341014-58341259	K562	blood:	n/a	n/a
3	ARID3A	chr11:58346988-58347660	HepG2	liver:	n/a	n/a
4	ARID3A	chr11:58344557-58346338	HepG2	liver:	n/a	n/a
5	ARID3A	chr11:58346978-58347892	K562	blood:	n/a	n/a
6	ATF1	chr11:58341149-58341349	K562	blood:	n/a	n/a
7	ATF1	chr11:58345105-58346583	K562	blood:	n/a	n/a
8	ATF2	chr11:58340773-58341736	GM12878	blood:	n/a	n/a
9	ATF2	chr11:58342845-58343710	GM12878	blood:	n/a	n/a
10	ATF2	chr11:58347706-58348152	GM12878	blood:	n/a	n/a
11	ATF2	chr11:58340789-58341768	GM12878	blood:	n/a	n/a
12	ATF2	chr11:58344664-58346570	GM12878	blood:	n/a	n/a
13	ATF2	chr11:58345615-58346559	H1-hESC	embryonic stem cell:	n/a	n/a
14	ATF2	chr11:58346858-58347654	GM12878	blood:	n/a	n/a
15	ATF2	chr11:58344499-58346651	GM12878	blood:	n/a	n/a
16	ATF2	chr11:58347715-58348202	GM12878	blood:	n/a	n/a
17	ATF2	chr11:58342764-58343577	GM12878	blood:	n/a	n/a
18	ATF2	chr11:58346951-58347705	GM12878	blood:	n/a	n/a
19	ATF3	chr11:58346996-58347489	HepG2	liver:	n/a	n/a
20	ATF3	chr11:58346944-58347435	A549	lung:	n/a	n/a
21	ATF3	chr11:58346985-58347312	HepG2	liver:	n/a	n/a
22	ATF3	chr11:58346991-58347293	H1-hESC	embryonic stem cell:	n/a	n/a
23	ATF3	chr11:58347086-58347337	GM12878	blood:	n/a	n/a
24	ATF3	chr11:58347016-58347452	H1-hESC	embryonic stem cell:	n/a	n/a
25	ATF3	chr11:58346926-58347392	GM12878	blood:	n/a	n/a
26	ATF3	chr11:58346900-58347469	A549	lung:	n/a	n/a
27	ATF3	chr11:58345599-58346375	A549	lung:	n/a	n/a
28	ATF3	chr11:58346929-58347330	K562	blood:	n/a	n/a
29	ATF3	chr11:58346985-58347545	K562	blood:	n/a	n/a
30	ATF3	chr11:58345348-58345903	K562	blood:	n/a	n/a
31	ATF3	chr11:58345084-58346020	K562	blood:	n/a	n/a
32	BACH1	chr11:58345634-58346589	H1-hESC	embryonic stem cell:	n/a	n/a
33	BACH1	chr11:58345738-58346211	K562	blood:	n/a	n/a
34	BATF	chr11:58347727-58348174	GM12878	blood:	n/a	n/a
35	BATF	chr11:58340930-58341359	GM12878	blood:	n/a	n/a
36	BATF	chr11:58340919-58341577	GM12878	blood:	n/a	n/a
37	BATF	chr11:58345625-58345921	GM12878	blood:	n/a	chr11:58345784-58345794
38	BATF	chr11:58344885-58345851	GM12878	blood:	n/a	chr11:58345784-58345794
39	BATF	chr11:58344979-58345313	GM12878	blood:	n/a	n/a
40	BATF	chr11:58345351-58345618	GM12878	blood:	n/a	n/a
41	BATF	chr11:58347037-58347408	GM12878	blood:	n/a	n/a
42	BATF	chr11:58343047-58343432	GM12878	blood:	n/a	n/a
43	BCL11A	chr11:58340919-58341526	GM12878	blood:	n/a	chr11:58341072-58341081 chr11:58341198-58341207
44	BCL11A	chr11:58340898-58341411	GM12878	blood:	n/a	chr11:58341072-58341081 chr11:58341198-58341207
45	BCL11A	chr11:58344956-58345711	GM12878	blood:	n/a	n/a
46	BCL11A	chr11:58344936-58345664	GM12878	blood:	n/a	n/a
47	BCL3	chr11:58346856-58347372	GM12878	blood:	n/a	n/a
48	BCL3	chr11:58345212-58346505	A549	lung:	n/a	n/a
49	BCL3	chr11:58340891-58341356	GM12878	blood:	n/a	chr11:58341072-58341081 chr11:58341198-58341207
50	BCL3	chr11:58346831-58347524	A549	lung:	n/a	n/a

(count:1408 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:58345705-58345755	HAEpiC	amniotic membrane:	n/a
2	chr11:58345608-58345658	Hepatocyte	liver:	n/a
3	chr11:58346531-58346581	PANC-1	pancreas:	n/a
4	chr11:58346138-58346188	BJ	skin:	n/a
5	chr11:58347088-58347138	GM06990	blood:	n/a
6	chr11:58345705-58345755	HAEpiC	amniotic membrane:	n/a
7	chr11:58345608-58345658	Hepatocyte	liver:	n/a
8	chr11:58346531-58346581	PANC-1	pancreas:	n/a
9	chr11:58346138-58346188	BJ	skin:	n/a
10	chr11:58347088-58347138	GM06990	blood:	n/a
11	chr11:58346524-58346574	H1-hESC	embryonic stem cell:	embryo
12	chr11:58345717-58345767	HAEpiC	amniotic membrane:	n/a
13	chr11:58345608-58345658	H1-hESC	embryonic stem cell:	embryo
14	chr11:58345608-58345658	Jurkat	blood:	n/a
15	chr11:58344244-58344294	HMEC	breast:	n/a
16	chr11:58346540-58346590	HCM	heart:	n/a
17	chr11:58347088-58347138	Hela-S3	cervix:	n/a
18	chr11:58346542-58346592	AG10803	skin:	n/a
19	chr11:58345717-58345767	HIPEpiC	eye:	n/a
20	chr11:58346540-58346590	HCPEpiC	choroid plexus:	n/a
21	chr11:58345702-58345752	HL-60	blood:	n/a
22	chr11:58347526-58347576	MCF-7	breast:	n/a
23	chr11:58347526-58347576	PANC-1	pancreas:	n/a
24	chr11:58346531-58346581	GM12878	blood:	n/a
25	chr11:58345695-58345745	PFSK-1	brain:	n/a
26	chr11:58345523-58345573	GM12891	blood:	n/a
27	chr11:58345523-58345573	HL-60	blood:	n/a
28	chr11:58345717-58345767	AG10803	skin:	n/a
29	chr11:58345287-58345337	NT2-D1	testis:	n/a
30	chr11:58347178-58347228	HUVEC	blood vessel:	n/a
31	chr11:58346540-58346590	AG09309	skin:	n/a
32	chr11:58345523-58345573	Hepatocyte	liver:	n/a
33	chr11:58347526-58347576	CMK	blood:	n/a
34	chr11:58347178-58347228	BJ	skin:	n/a
35	chr11:58346138-58346188	H1-hESC	embryonic stem cell:	embryo
36	chr11:58347526-58347576	NB4	blood:	n/a
37	chr11:58345717-58345767	HPAEpiC	pulmonary alveolar:	n/a
38	chr11:58343791-58343841	ovcar-3	ovarian:	n/a
39	chr11:58345705-58345755	SAEC	small airway:	n/a
40	chr11:58346540-58346590	ovcar-3	ovarian:	n/a
41	chr11:58346531-58346581	ProgFib	skin:	n/a
42	chr11:58345695-58345745	HIPEpiC	eye:	n/a
43	chr11:58346524-58346574	AG04449	skin:	fetal
44	chr11:58346138-58346188	SK-N-SH	brain:	n/a
45	chr11:58345226-58345276	HNPCEpiC	eye:	n/a
46	chr11:58345705-58345755	HCF	heart:	n/a
47	chr11:58347526-58347576	HMEC	breast:	n/a
48	chr11:58345705-58345755	HRPEpiC	eye:	n/a
49	chr11:58345687-58345737	HNPCEpiC	eye:	n/a
50	chr11:58346542-58346592	U87	brain:	n/a

(count:39 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:58345437..58346957-chr4:7043706..7045674,2	K562	blood:
2	chr11:58345131..58348848-chr11:58387112..58390850,4	K562	blood:
3	chr11:58337361..58338941-chr11:58344525..58347399,2	MCF-7	breast:
4	chr11:58346671..58347279-chr11:58397113..58398063,2	MCF-7	breast:
5	chr11:58340817..58343050-chr11:58387964..58391771,3	K562	blood:
6	chr11:58345920..58346638-chr17:26988735..26989426,3	Hela-S3	cervix:
7	chr11:58345242..58347401-chr14:50233763..50235368,2	MCF-7	breast:
8	chr11:58345634..58347329-chr11:58913905..58915748,2	MCF-7	breast:
9	chr11:58308273..58310053-chr11:58338250..58340152,2	K562	blood:
10	chr11:58345286..58347963-chr11:58389614..58393452,3	MCF-7	breast:
11	chr11:57297015..57298977-chr11:58345779..58348496,3	K562	blood:
12	chr1:156630989..156631533-chr11:58345269..58345934,2	HCT-116	colon:
13	chr11:57433251..57437103-chr11:58344962..58348416,5	K562	blood:
14	chr11:58345021..58345588-chr3:129034227..129035062,2	Hela-S3	cervix:
15	chr11:57423476..57425127-chr11:58344978..58347964,2	K562	blood:
16	chr11:58344606..58345552-chr11:58442971..58443635,2	K562	blood:
17	chr11:58344628..58346130-chr11:58388841..58391574,2	MCF-7	breast:
18	chr11:58344188..58345053-chr11:58555383..58556475,3	MCF-7	breast:
19	chr11:58343669..58348848-chr11:58387112..58391418,8	K562	blood:
20	chr11:58346682..58349272-chr11:58349301..58352571,4	MCF-7	breast:
21	chr11:58343237..58345881-chr11:58936566..58939542,2	K562	blood:
22	chr11:58346682..58347411-chr8:128233331..128233832,2	Hela-S3	cervix:
23	chr11:58332917..58335561-chr11:58336886..58338448,2	K562	blood:
24	chr1:8762975..8763667-chr11:58346673..58347454,2	NB4	blood:
25	chr11:58341513..58344415-chr11:58344785..58347272,2	MCF-7	breast:
26	chr11:58334595..58336830-chr11:58344881..58347301,2	MCF-7	breast:
27	chr1:145382494..145383212-chr11:58345288..58345852,2	Hela-S3	cervix:
28	chr11:57434798..57437115-chr11:58345701..58348083,4	MCF-7	breast:
29	chr11:58341513..58344415-chr11:58344785..58347272,2	MCF-7	breast:
30	chr11:58346677..58347271-chr17:41438125..41438855,2	Hela-S3	cervix:
31	chr11:57433251..57435131-chr11:58346916..58348765,2	K562	blood:
32	chr11:58334129..58337233-chr11:58345487..58348249,3	MCF-7	breast:
33	chr11:58340835..58343059-chr11:58344433..58346364,2	MCF-7	breast:
34	chr1:37939974..37940671-chr11:58346171..58346779,2	Hela-S3	cervix:
35	chr11:58347130..58349444-chr11:58352908..58354763,3	MCF-7	breast:
36	chr11:58345815..58346705-chr19:45971168..45971770,2	Hela-S3	cervix:
37	chr11:58344216..58344800-chr11:58397105..58397970,2	MCF-7	breast:
38	chr11:58344715..58345686-chr12:123011120..123011802,2	Hela-S3	cervix:
39	chr11:58292350..58294011-chr11:58343691..58345375,2	K562	blood:

No data

Variant related genes	Relation type
ZFP91-CNTF	TF binding region
ZFP91	TF binding region
LPXN	TF binding region
ZFP91-CNTF	CpG island
ZFP91	CpG island
LPXN	CpG island
ENSG00000186660	chromatin interactions
ENSG00000166801	chromatin interactions
ENSG00000229953	chromatin interactions
ENSG00000111011	chromatin interactions
ENSG00000132581	chromatin interactions
ENSG00000184445	chromatin interactions
ENSG00000109111	chromatin interactions
ENSG00000172409	chromatin interactions
ENSG00000255073	chromatin interactions
ENSG00000125740	chromatin interactions
ENSG00000134809	chromatin interactions
ENSG00000233621	chromatin interactions
ENSG00000110042	chromatin interactions
ENSG00000201558	chromatin interactions
ENSG00000242689	chromatin interactions
ENSG00000110031	chromatin interactions
ENSG00000173013	chromatin interactions
ENSG00000156599	chromatin interactions
ENSG00000142599	chromatin interactions
ENSG00000206417	chromatin interactions
ENSG00000173011	chromatin interactions
ENSG00000163874	chromatin interactions
ENSG00000165516	chromatin interactions

Extended variants
information (count: 458 )
Associated
traits (count: 51 )

Variant overlapped rSNPs/rCNVs (count:458 , 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	rs7115061	chr11:58336620-58336621	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs183544967	chr11:58336630-58336631	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs557894231	chr11:58336665-58336666	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs570152493	chr11:58336671-58336672	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs140481973	chr11:58336678-58336679	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs377054725	chr11:58336679-58336680	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs539920685	chr11:58336693-58336694	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs554994390	chr11:58336697-58336698	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs145721729	chr11:58336735-58336736	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs544492120	chr11:58336738-58336739	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs562644275	chr11:58336757-58336758	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs533229252	chr11:58336761-58336762	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs545239233	chr11:58336829-58336830	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs11229529	chr11:58336851-58336852	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	mRNA abundance
15	rs138305062	chr11:58336861-58336862	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs574952209	chr11:58336863-58336864	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs576257426	chr11:58336923-58336924	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs547105852	chr11:58336946-58336947	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs138323634	chr11:58336967-58336968	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs367917687	chr11:58336971-58336972	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs12362218	chr11:58337024-58337025	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs529272746	chr11:58337027-58337028	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs187885835	chr11:58337053-58337054	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs569462588	chr11:58337068-58337069	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs199608808	chr11:58337104-58337105	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs539726308	chr11:58337109-58337110	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs141068123	chr11:58337148-58337149	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs376031559	chr11:58337189-58337190	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs529401025	chr11:58337273-58337274	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs566723045	chr11:58337286-58337287	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs190867388	chr11:58337289-58337290	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs555182341	chr11:58337293-58337294	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs112121686	chr11:58337325-58337326	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs34675222	chr11:58337331-58337332	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs373922599	chr11:58337358-58337359	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs138864221	chr11:58337417-58337418	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs572249715	chr11:58337489-58337490	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs578025622	chr11:58337499-58337500	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs540777551	chr11:58337505-58337506	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs545318994	chr11:58337509-58337510	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs560429426	chr11:58337519-58337520	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs572278369	chr11:58337547-58337548	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs61889509	chr11:58337548-58337549	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs149432839	chr11:58337555-58337556	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs530652878	chr11:58337605-58337606	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs377380084	chr11:58337647-58337648	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs550730225	chr11:58337745-58337746	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs368257803	chr11:58337793-58337794	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs562876666	chr11:58337794-58337795	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs202219415	chr11:58337807-58337808	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:51)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Autism	22495311	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Glioblastoma multiforme	21138945	CNVD
Esophageal cancer	21851588	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Glioblastoma multiforme	22286061	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
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Colorectal cancer	16272173	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Pituitary adenoma	18645599	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Prostate cancer	18632612	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Smith-Lemli-Opitz syndrome	21572526	CNVD
Multiple myeloma	16461302	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Autism	22495309	CNVD
Autism	20808228	CNVD
Melanoma	17363583	CNVD

Chromatin state (count:919 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:58300000-58340600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
2	chr11:58300600-58338600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr11:58309600-58338800	Strong transcription	Primary monocytes fromperipheralblood	blood
4	chr11:58315600-58340400	Weak transcription	Stomach Mucosa	stomach
5	chr11:58318400-58341000	Weak transcription	Right Ventricle	heart
6	chr11:58318400-58344800	Weak transcription	Fetal Brain Male	brain
7	chr11:58318600-58344400	Weak transcription	Placenta Amnion	Placenta Amnion
8	chr11:58318800-58336800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr11:58318800-58340600	Weak transcription	NHLF	lung
10	chr11:58318800-58341400	Weak transcription	Psoas Muscle	Psoas
11	chr11:58319200-58343000	Weak transcription	Fetal Brain Female	brain
12	chr11:58320000-58341000	Weak transcription	HSMMtube	muscle
13	chr11:58320200-58340800	Weak transcription	Colon Smooth Muscle	Colon
14	chr11:58320600-58338200	Weak transcription	HMEC	breast
15	chr11:58321600-58337200	Weak transcription	Rectal Smooth Muscle	rectum
16	chr11:58321600-58340400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
17	chr11:58321800-58340400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
18	chr11:58321800-58341200	Weak transcription	Colonic Mucosa	Colon
19	chr11:58321800-58345000	Weak transcription	Ovary	ovary
20	chr11:58322200-58337000	Weak transcription	Primary neutrophils fromperipheralblood	blood
21	chr11:58322400-58336800	Weak transcription	Spleen	Spleen
22	chr11:58322400-58344200	Weak transcription	Fetal Lung	lung
23	chr11:58329400-58341000	Weak transcription	Brain Angular Gyrus	brain
24	chr11:58329400-58342600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
25	chr11:58329400-58344400	Weak transcription	Cortex derived primary cultured neurospheres	brain
26	chr11:58330200-58343000	Weak transcription	Fetal Kidney	kidney
27	chr11:58330400-58336800	Weak transcription	Pancreas	Pancrea
28	chr11:58330400-58338800	Genic enhancers	Primary T helper cells PMA-I stimulated	--
29	chr11:58330600-58345000	Weak transcription	Gastric	stomach
30	chr11:58331000-58338000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
31	chr11:58331400-58341000	Weak transcription	Duodenum Smooth Muscle	Duodenum
32	chr11:58332800-58340200	Weak transcription	Primary hematopoietic stem cells	blood
33	chr11:58334200-58337000	Genic enhancers	Primary T helper memory cells from peripheral blood 1	blood
34	chr11:58334200-58337000	Genic enhancers	Primary T helper 17 cells PMA-I stimulated	--
35	chr11:58334400-58338200	Strong transcription	HSMM	muscle
36	chr11:58334600-58338400	Genic enhancers	Primary T helper naive cells from peripheral blood	blood
37	chr11:58334800-58339600	Genic enhancers	Primary T helper cells fromperipheralblood	blood
38	chr11:58335000-58336800	Genic enhancers	NHDF-Ad	bronchial
39	chr11:58335000-58337400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
40	chr11:58335000-58338600	Genic enhancers	Primary T helper naive cells fromperipheralblood	blood
41	chr11:58335400-58338800	Genic enhancers	Primary T cells fromperipheralblood	blood
42	chr11:58335600-58340400	Weak transcription	Brain Hippocampus Middle	brain
43	chr11:58335800-58339800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
44	chr11:58335800-58340400	Weak transcription	Hela-S3	cervix
45	chr11:58336000-58336800	Genic enhancers	Primary T cells from cord blood	blood
46	chr11:58336000-58337200	Genic enhancers	Primary hematopoietic stem cells short term culture	blood
47	chr11:58336000-58337400	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
48	chr11:58336000-58337600	Strong transcription	Adipose Nuclei	Adipose
49	chr11:58336000-58338200	Strong transcription	Brain Cingulate Gyrus	brain
50	chr11:58336000-58338400	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood

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