Variant report

Variant	nsv984475
Chromosome Location	chr11:75891800-75943874
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1229)
CpG islands
(count:2322)
Chromatin interactive
region (count:83)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1229 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:75919860-75920108	HepG2	liver:	n/a	n/a
2	ATF2	chr11:75943107-75943508	GM12878	blood:	n/a	n/a
3	ATF3	chr11:75919783-75920220	A549	lung:	n/a	n/a
4	ATF3	chr11:75919853-75920215	A549	lung:	n/a	n/a
5	BACH1	chr11:75921380-75922316	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr11:75918709-75918900	K562	blood:	n/a	n/a
7	BACH1	chr11:75916750-75916926	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr11:75919833-75920847	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr11:75918583-75919316	H1-hESC	embryonic stem cell:	n/a	n/a
10	BCL3	chr11:75918338-75918916	A549	lung:	n/a	chr11:75918813-75918822
11	BCL3	chr11:75919791-75920256	A549	lung:	n/a	chr11:75919827-75919836
12	BHLHE40	chr11:75918652-75918875	HepG2	liver:	n/a	n/a
13	BHLHE40	chr11:75895960-75896047	K562	blood:	n/a	n/a
14	BHLHE40	chr11:75918605-75918909	K562	blood:	n/a	n/a
15	BHLHE40	chr11:75917372-75917610	K562	blood:	n/a	chr11:75917535-75917551
16	BHLHE40	chr11:75943132-75943454	GM12878	blood:	n/a	n/a
17	BHLHE40	chr11:75921554-75922195	HepG2	liver:	n/a	chr11:75921944-75921960 chr11:75921941-75921957
18	BHLHE40	chr11:75917520-75917589	GM12878	blood:	n/a	chr11:75917535-75917551
19	BHLHE40	chr11:75942808-75942848	GM12878	blood:	n/a	n/a
20	BHLHE40	chr11:75919847-75920073	GM12878	blood:	n/a	n/a
21	BHLHE40	chr11:75918623-75918961	GM12878	blood:	n/a	n/a
22	BRCA1	chr11:75919889-75920503	Hela-S3	cervix:	n/a	n/a
23	BRCA1	chr11:75917362-75917369	Hela-S3	cervix:	n/a	n/a
24	BRCA1	chr11:75943274-75943306	GM12878	blood:	n/a	n/a
25	BRCA1	chr11:75918536-75918947	Hela-S3	cervix:	n/a	n/a
26	CBX3	chr11:75917274-75917681	K562	blood:	n/a	n/a
27	CBX3	chr11:75935842-75936132	K562	blood:	n/a	n/a
28	CBX3	chr11:75918218-75918990	K562	blood:	n/a	n/a
29	CCNT2	chr11:75895841-75896045	K562	blood:	n/a	n/a
30	CCNT2	chr11:75936354-75936549	K562	blood:	n/a	n/a
31	CCNT2	chr11:75918618-75918977	K562	blood:	n/a	chr11:75918965-75918974
32	CCNT2	chr11:75917343-75917789	K562	blood:	n/a	n/a
33	CEBPB	chr11:75895861-75896066	K562	blood:	n/a	n/a
34	CEBPB	chr11:75937717-75938031	Hela-S3	cervix:	n/a	chr11:75937861-75937872
35	CEBPB	chr11:75917020-75917495	Hela-S3	cervix:	n/a	n/a
36	CEBPB	chr11:75917830-75918975	Hela-S3	cervix:	n/a	n/a
37	CEBPB	chr11:75918279-75918452	K562	blood:	n/a	n/a
38	CEBPB	chr11:75926220-75926516	HepG2	liver:	n/a	chr11:75926377-75926388
39	CEBPB	chr11:75937691-75938043	HepG2	liver:	n/a	chr11:75937861-75937872
40	CEBPB	chr11:75919827-75920136	Hela-S3	cervix:	n/a	n/a
41	CEBPB	chr11:75937829-75937917	H1-hESC	embryonic stem cell:	n/a	chr11:75937861-75937872
42	CEBPB	chr11:75937682-75938057	K562	blood:	n/a	chr11:75937861-75937872
43	CEBPB	chr11:75918226-75919076	H1-hESC	embryonic stem cell:	n/a	n/a
44	CEBPB	chr11:75918206-75918835	K562	blood:	n/a	n/a
45	CEBPB	chr11:75937705-75938029	A549	lung:	n/a	chr11:75937861-75937872
46	CEBPB	chr11:75933448-75933618	Hela-S3	cervix:	n/a	n/a
47	CEBPB	chr11:75933023-75933050	A549	lung:	n/a	n/a
48	CEBPB	chr11:75932923-75933121	K562	blood:	n/a	n/a
49	CEBPB	chr11:75937688-75938100	MCF-7	breast:	n/a	chr11:75937861-75937872
50	CEBPB	chr11:75901486-75901900	IMR90	lung:	n/a	n/a

(count:2322 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:75909015-75909065	HNPCEpiC	eye:	n/a
2	chr11:75919862-75919912	GM12891	blood:	n/a
3	chr11:75905917-75905967	HIPEpiC	eye:	n/a
4	chr11:75917844-75917894	HRCEpiC	kidney:	n/a
5	chr11:75909015-75909065	HNPCEpiC	eye:	n/a
6	chr11:75919862-75919912	GM12891	blood:	n/a
7	chr11:75905917-75905967	HIPEpiC	eye:	n/a
8	chr11:75917844-75917894	HRCEpiC	kidney:	n/a
9	chr11:75917982-75918032	Hela-S3	cervix:	n/a
10	chr11:75918630-75918680	HCM	heart:	n/a
11	chr11:75922172-75922222	NH-A	brain:	n/a
12	chr11:75917404-75917454	ECC-1	luminal epithelium:	n/a
13	chr11:75902270-75902320	BE2_C	brain:	n/a
14	chr11:75917353-75917403	NHDF-neo	bronchial:	n/a
15	chr11:75921808-75921858	HRPEpiC	eye:	n/a
16	chr11:75909015-75909065	Hepatocyte	liver:	n/a
17	chr11:75922637-75922687	K562	blood:	n/a
18	chr11:75918089-75918139	ProgFib	skin:	n/a
19	chr11:75916460-75916510	H1-hESC	embryonic stem cell:	embryo
20	chr11:75924614-75924664	HEEpiC	esophagus:	n/a
21	chr11:75917251-75917301	HCT-116	colon:	n/a
22	chr11:75897427-75897477	SKMC	muscle:	n/a
23	chr11:75921810-75921860	HRE	kidney:	n/a
24	chr11:75919130-75919180	SK-N-SH	brain:	n/a
25	chr11:75917982-75918032	AG09309	skin:	n/a
26	chr11:75918089-75918139	HL-60	blood:	n/a
27	chr11:75921940-75921990	K562	blood:	n/a
28	chr11:75921433-75921483	GM12878	blood:	n/a
29	chr11:75905718-75905768	NHBE	bronchial:	n/a
30	chr11:75919698-75919748	GM12892	blood:	n/a
31	chr11:75917353-75917403	HRE	kidney:	n/a
32	chr11:75904184-75904234	HL-60	blood:	n/a
33	chr11:75922172-75922222	AG09309	skin:	n/a
34	chr11:75898203-75898253	SAEC	small airway:	n/a
35	chr11:75898132-75898182	ECC-1	luminal epithelium:	n/a
36	chr11:75919698-75919748	GM19239	blood:	n/a
37	chr11:75943228-75943278	BJ	skin:	n/a
38	chr11:75918630-75918680	HIPEpiC	eye:	n/a
39	chr11:75897427-75897477	HUVEC	blood vessel:	n/a
40	chr11:75924614-75924664	ovcar-3	ovarian:	n/a
41	chr11:75920233-75920283	SK-N-SH	brain:	n/a
42	chr11:75896332-75896382	LNCaP	prostate:	n/a
43	chr11:75909015-75909065	Jurkat	blood:	n/a
44	chr11:75917251-75917301	HEK293	kidney:	embryo
45	chr11:75917982-75918032	H1-hESC	embryonic stem cell:	embryo
46	chr11:75919698-75919748	HL-60	blood:	n/a
47	chr11:75897427-75897477	SK-N-SH	brain:	n/a
48	chr11:75914370-75914420	HEK293	kidney:	embryo
49	chr11:75919862-75919912	H1-hESC	embryonic stem cell:	embryo
50	chr11:75921940-75921990	GM12892	blood:	n/a

(count:83 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr11:75911614..75914237-chr11:75920875..75922850,2	MCF-7	breast:
2	chr11:75918308..75919483-chr11:76029559..76030293,4	MCF-7	breast:
3	chr11:75895372..75898295-chr11:75906346..75908229,2	K562	blood:
4	chr11:75927881..75933207-chr11:75943670..75948340,7	K562	blood:
5	chr11:75901629..75903680-chr11:75921082..75923446,2	K562	blood:
6	chr11:75918395..75919729-chr11:75947370..75948224,3	K562	blood:
7	chr11:75879470..75881382-chr11:75903439..75906024,2	MCF-7	breast:
8	chr11:75891012..75893171-chr11:75895940..75897806,2	K562	blood:
9	chr11:75918665..75919393-chr11:76002890..76003539,3	MCF-7	breast:
10	chr11:75918335..75919414-chr11:76029518..76030460,11	K562	blood:
11	chr11:75919561..75922222-chr11:75927095..75929446,2	MCF-7	breast:
12	chr11:75918322..75919263-chr11:76029385..76030419,7	MCF-7	breast:
13	chr11:75892849..75895480-chr11:75897932..75899434,2	K562	blood:
14	chr11:75895372..75898295-chr11:75906346..75908229,2	K562	blood:
15	chr1:156698046..156698801-chr11:75908969..75909469,2	Hela-S3	cervix:
16	chr11:75918753..75920332-chr11:75923652..75925664,2	K562	blood:
17	chr11:75935715..75937610-chr11:75945904..75948559,2	K562	blood:
18	chr11:75920940..75923534-chr11:75938310..75940722,2	K562	blood:
19	chr11:75941641..75943721-chr11:76090147..76092778,2	MCF-7	breast:
20	chr11:75886596..75888940-chr11:75889618..75892110,2	MCF-7	breast:
21	chr11:75918587..75919130-chr11:76223991..76224816,2	MCF-7	breast:
22	chr11:75895025..75897686-chr11:75910991..75913944,2	K562	blood:
23	chr11:75907802..75910235-chr11:75912499..75914692,2	K562	blood:
24	chr11:75918865..75921360-chr11:76155223..76156994,2	MCF-7	breast:
25	chr11:75901629..75903680-chr11:75921082..75923446,2	K562	blood:
26	chr11:75902153..75903768-chr11:75945033..75947723,2	K562	blood:
27	chr11:75918371..75919261-chr11:76391667..76392614,4	MCF-7	breast:
28	chr11:75917231..75918975-chr11:75929986..75933307,3	K562	blood:
29	chr11:75918366..75919493-chr11:76391585..76392458,3	K562	blood:
30	chr11:75907463..75909415-chr11:75917684..75920104,2	MCF-7	breast:
31	chr11:75913612..75915944-chr11:75916007..75917749,2	K562	blood:
32	chr11:75862934..75863810-chr11:75918354..75919268,2	K562	blood:
33	chr11:75607577..75608491-chr11:75919794..75920666,2	MCF-7	breast:
34	chr11:75913174..75915616-chr11:76090569..76092152,2	MCF-7	breast:
35	chr11:75934327..75936771-chr11:75938292..75940833,2	K562	blood:
36	chr11:75913811..75916068-chr11:75920291..75921987,2	K562	blood:
37	chr11:75919700..75922037-chr11:76092044..76093720,2	MCF-7	breast:
38	chr11:75895025..75897686-chr11:75910991..75913944,2	K562	blood:
39	chr11:75924146..75926385-chr11:76032779..76035393,2	MCF-7	breast:
40	chr11:75917185..75919350-chr11:75920586..75922926,4	K562	blood:
41	chr11:75916539..75918756-chr11:75919573..75922083,2	MCF-7	breast:
42	chr11:75892849..75895759-chr11:75897789..75899434,2	K562	blood:
43	chr11:75888382..75891358-chr11:75893738..75896231,2	MCF-7	breast:
44	chr11:75919323..75921624-chr11:75923992..75926827,3	MCF-7	breast:
45	chr11:75892849..75895759-chr11:75897789..75899434,2	K562	blood:
46	chr11:75908679..75911274-chr11:75914998..75917762,2	K562	blood:
47	chr11:75934214..75936771-chr11:75938292..75941222,2	K562	blood:
48	chr11:75916539..75918756-chr11:75919573..75922083,2	MCF-7	breast:
49	chr11:75892849..75895480-chr11:75897932..75899434,2	K562	blood:
50	chr11:75927881..75933207-chr11:75943670..75948340,7	K562	blood:

(count:7 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-UVRAG-2	chr11:75901769-75901950	ENSG00000254933.1
2	lnc-UVRAG-2	chr11:75905685-75906115	ENSG00000254933.1
3	lnc-WNT11-1	chr11:75927031-75927069	ENSG00000255362
4	lnc-PRKRIR-3	chr11:75917466-75917542	NONHSAT023149
5	lnc-WNT11-1	chr11:75922000-75922293	ENSG00000255362
6	lnc-PRKRIR-3	chr11:75921391-75921774	NONHSAT023149
7	lnc-WNT11-1	chr11:75926282-75926336	ENSG00000255362

No data

Variant related genes	Relation type
WNT11	TF binding region
ENSG00000255362	TF binding region
ENSG00000254933	TF binding region
WNT11	CpG island
ENSG00000255362	CpG island
ENSG00000254933	CpG island
ENSG00000152518	chromatin interactions
ENSG00000137492	chromatin interactions
ENSG00000254933	chromatin interactions
ENSG00000143319	chromatin interactions
ENSG00000143303	chromatin interactions
ENSG00000179240	chromatin interactions
ENSG00000085741	chromatin interactions
ENSG00000158636	chromatin interactions
ENSG00000255135	chromatin interactions

Extended variants
information (count: 2058 )
Associated
traits (count: 99 )

Variant overlapped rSNPs/rCNVs (count:2058 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs148033598	chr11:75891807-75891808	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
2	rs533973956	chr11:75891808-75891809	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
3	rs60349325	chr11:75891850-75891851	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
4	rs539198897	chr11:75891878-75891879	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
5	rs558788887	chr11:75891886-75891887	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
6	rs139274966	chr11:75891901-75891902	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
7	rs145446301	chr11:75891945-75891946	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
8	rs78031141	chr11:75891983-75891984	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
9	rs574722062	chr11:75892004-75892005	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs543666860	chr11:75892026-75892027	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs542536737	chr11:75892059-75892060	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs369520561	chr11:75892079-75892080	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs552815861	chr11:75892121-75892122	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs572711324	chr11:75892147-75892148	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs565436932	chr11:75892221-75892222	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs544758138	chr11:75892235-75892236	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs564928680	chr11:75892242-75892243	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs373030447	chr11:75892250-75892251	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs530670100	chr11:75892268-75892269	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs532880715	chr11:75892303-75892304	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs140880026	chr11:75892313-75892314	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs12363352	chr11:75892318-75892319	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs144841877	chr11:75892346-75892347	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs547331389	chr11:75892376-75892377	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs191439835	chr11:75892390-75892391	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs145852516	chr11:75892412-75892413	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs570028277	chr11:75892468-75892469	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs149002233	chr11:75892478-75892479	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs538366620	chr11:75892555-75892556	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs537447838	chr11:75892567-75892568	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs151020058	chr11:75892577-75892578	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs377639210	chr11:75892607-75892608	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs554739013	chr11:75892608-75892609	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs371103649	chr11:75892626-75892627	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs533891938	chr11:75892660-75892661	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs376026416	chr11:75892676-75892677	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs572848643	chr11:75892686-75892687	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs544964807	chr11:75892705-75892706	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs647159	chr11:75892741-75892742	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs143838984	chr11:75892751-75892752	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs544314236	chr11:75892752-75892753	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs370090626	chr11:75892758-75892759	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs73500076	chr11:75892793-75892794	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs113360758	chr11:75892818-75892819	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs183795215	chr11:75892873-75892874	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs538956702	chr11:75892886-75892887	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs150929846	chr11:75893005-75893006	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs532893284	chr11:75893148-75893149	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs553661020	chr11:75893178-75893179	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs571930946	chr11:75893193-75893194	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:99)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Wilms tumour	21544195	CNVD
Autism	22495311	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Glioblastoma multiforme	21138945	CNVD
Acute myeloid leukemia	20729466	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	21637783	CNVD
Acute myeloid leukemia	16864856	CNVD
Chronic lymphocytic leukemia	21795749	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21484798	CNVD
Ewing''s sarcoma	21437220	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	20837533	CNVD
Breast cancer	21264507	CNVD
Cervical cancer	21063398	CNVD
Glioblastoma multiforme	19960244	CNVD
Liposarcoma	21253554	CNVD
Neuroblastoma	18923524	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Neuroblastoma	17533364	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Prostate cancer	18632612	CNVD
Smith-Lemli-Opitz syndrome	21572526	CNVD
Glioblastoma multiforme	21080181	CNVD
Multiple myeloma	16461302	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Melanoma	18172304	CNVD
Breast cancer	22002566	CNVD
Ductal carcinoma	18381933	CNVD
Retinoblastoma	22278416	CNVD
Breast cancer	20953835	CNVD
oto-dental syndrome	17656375	CNVD
Asthma	21956041	CNVD
Breast cancer	17603634	CNVD
Ovarian neoplasms	16753589	CNVD
Non-small cell lung cancer	20864512	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cervical cancer	21062161	CNVD
Breast cancer	21509527	CNVD
Breast cancer	17001317	CNVD
Oral squamous cell carcinoma	16619035	CNVD
Intracranial aneurysm	16715129	CNVD
Colorectal cancer	16272173	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Colorectal cancer	16882699	CNVD
Berardinelli-seip congenital generalized lipodystrophy	17668395	CNVD
Spinal muscular atrophy	17668395	CNVD
Neonatal seizures	17668395	CNVD
Neonatal seizures	17668391	CNVD
Neuroticism	17667963	CNVD
Cancer	17916600	CNVD
Squamous cell cancer	19047905	CNVD
Multiple endocrine neoplasia type 1	19566914	CNVD
XY sex reversal	17503084	CNVD
Berardinelli-seip congenital generalized lipodystrophy	17668391	CNVD
Maculopathy	17646752	CNVD
Breast cancer	17899364	CNVD
Breast cancer	17157792	CNVD
Esophageal squamous carcinoma	18350619	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
lymphocytic leukemia	21291569	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Cancer	22183965	CNVD
Melanoma	22183965	CNVD
Breast cancer	16620391	CNVD
Multiple myeloma	17550852	CNVD
Neuroblastoma	18923191	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Multiple myeloma	16616336	CNVD
Myelofibrosis	22110671	CNVD
Prostate cancer	17217626	CNVD
Cancer	22429812	CNVD
small cell lung cancer	20016488	CNVD
Acute myeloid leukemia	21251322	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21482786	CNVD
Ovarian cancer	20844748	CNVD
Breast cancer	16608533	CNVD
Usher syndrome	18421352	CNVD
Breast cancer	21858162	CNVD
Ovarian cancer	21240255	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1603 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:75883600-75897000	Weak transcription	Fetal Intestine Small	intestine
2	chr11:75887600-75892000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
3	chr11:75887800-75896400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
4	chr11:75888200-75895200	Weak transcription	HUES6 Cell Line	embryonic stem cell
5	chr11:75888800-75894800	Weak transcription	Fetal Lung	lung
6	chr11:75890600-75897000	Weak transcription	Gastric	stomach
7	chr11:75890800-75891800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr11:75890800-75895200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
9	chr11:75891000-75891800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr11:75891000-75896000	Weak transcription	Placenta Amnion	Placenta Amnion
11	chr11:75891200-75891800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr11:75891200-75892000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
13	chr11:75891200-75892400	Enhancers	Fetal Muscle Trunk	muscle
14	chr11:75891400-75892000	Enhancers	HepG2	liver
15	chr11:75891400-75892200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr11:75891600-75891800	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
17	chr11:75891800-75892000	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
18	chr11:75891800-75893400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
19	chr11:75891800-75893600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
20	chr11:75892000-75892800	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
21	chr11:75892000-75894600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
22	chr11:75892200-75892800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr11:75892200-75895200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
24	chr11:75892400-75895400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
25	chr11:75892800-75893800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
26	chr11:75893200-75893400	Enhancers	Pancreas	Pancrea
27	chr11:75893200-75895600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
28	chr11:75893400-75898000	Weak transcription	Pancreas	Pancrea
29	chr11:75893400-75902600	Enhancers	Placenta	Placenta
30	chr11:75893600-75894800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
31	chr11:75893800-75895600	Enhancers	K562	blood
32	chr11:75893800-75896000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
33	chr11:75894000-75896000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
34	chr11:75894200-75894600	Bivalent Enhancer	Fetal Muscle Leg	muscle
35	chr11:75894200-75898400	Enhancers	Fetal Heart	heart
36	chr11:75894400-75895800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
37	chr11:75894600-75894800	Enhancers	H1 Cell Line	embryonic stem cell
38	chr11:75894600-75896600	Enhancers	Skeletal Muscle Male	skeletal muscle
39	chr11:75894600-75897800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
40	chr11:75894600-75898200	Enhancers	Fetal Muscle Leg	muscle
41	chr11:75894800-75895000	Enhancers	Spleen	Spleen
42	chr11:75894800-75895200	Strong transcription	Fetal Lung	lung
43	chr11:75894800-75895600	Weak transcription	H1 Cell Line	embryonic stem cell
44	chr11:75894800-75897200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
45	chr11:75894800-75898400	Enhancers	Lung	lung
46	chr11:75895000-75896000	Weak transcription	Spleen	Spleen
47	chr11:75895000-75896600	Enhancers	Primary hematopoietic stem cells	blood
48	chr11:75895000-75897200	Enhancers	Primary hematopoietic stem cells short term culture	blood
49	chr11:75895000-75898400	Enhancers	HSMMtube	muscle
50	chr11:75895200-75896200	Enhancers	Skeletal Muscle Female	skeletal muscle

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