Variant report

Variant	nsv898184
Chromosome Location	chr11:93741612-93969726
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2669)
CpG islands
(count:3297)
Chromatin interactive
region (count:99)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:3)

(count:2669 , 50 per page) page: 1 2 3 4 5 6 7 ... 54

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:93884527-93884708	HepG2	liver:	n/a	n/a
2	ARID3A	chr11:93934157-93934699	HepG2	liver:	n/a	n/a
3	ARID3A	chr11:93849537-93849719	HepG2	liver:	n/a	n/a
4	ARID3A	chr11:93757847-93758051	K562	blood:	n/a	n/a
5	ARID3A	chr11:93863941-93864082	HepG2	liver:	n/a	n/a
6	ARID3A	chr11:93916976-93917325	HepG2	liver:	n/a	n/a
7	ARID3A	chr11:93868971-93869805	K562	blood:	n/a	n/a
8	ARID3A	chr11:93861663-93862073	HepG2	liver:	n/a	n/a
9	ARID3A	chr11:93864874-93865280	K562	blood:	n/a	n/a
10	ARID3A	chr11:93953706-93953959	HepG2	liver:	n/a	n/a
11	ARID3A	chr11:93840637-93840874	K562	blood:	n/a	n/a
12	ARID3A	chr11:93861882-93862074	K562	blood:	n/a	n/a
13	ARID3A	chr11:93885276-93885716	HepG2	liver:	n/a	n/a
14	ARID3A	chr11:93811045-93811359	K562	blood:	n/a	n/a
15	ARID3A	chr11:93932567-93932629	HepG2	liver:	n/a	n/a
16	ARID3A	chr11:93868385-93868684	K562	blood:	n/a	n/a
17	ARID3A	chr11:93887802-93887881	HepG2	liver:	n/a	n/a
18	ARID3A	chr11:93885221-93885691	K562	blood:	n/a	n/a
19	ATF1	chr11:93779579-93779886	K562	blood:	n/a	n/a
20	ATF1	chr11:93778579-93778710	K562	blood:	n/a	n/a
21	ATF1	chr11:93869143-93869767	K562	blood:	n/a	n/a
22	ATF1	chr11:93875524-93875811	K562	blood:	n/a	n/a
23	ATF1	chr11:93757089-93757299	K562	blood:	n/a	n/a
24	ATF1	chr11:93865037-93865267	K562	blood:	n/a	n/a
25	ATF1	chr11:93861837-93862135	K562	blood:	n/a	n/a
26	ATF1	chr11:93810981-93811392	K562	blood:	n/a	n/a
27	ATF1	chr11:93885418-93885765	K562	blood:	n/a	n/a
28	ATF1	chr11:93754009-93754142	K562	blood:	n/a	n/a
29	ATF2	chr11:93861575-93862043	GM12878	blood:	n/a	n/a
30	ATF2	chr11:93861710-93862375	GM12878	blood:	n/a	n/a
31	ATF2	chr11:93861539-93862091	H1-hESC	embryonic stem cell:	n/a	n/a
32	ATF2	chr11:93861445-93861731	H1-hESC	embryonic stem cell:	n/a	n/a
33	ATF3	chr11:93885506-93885690	K562	blood:	n/a	n/a
34	ATF3	chr11:93862257-93862541	K562	blood:	n/a	chr11:93862383-93862392
35	ATF3	chr11:93885400-93885775	K562	blood:	n/a	n/a
36	ATF3	chr11:93869126-93869742	K562	blood:	n/a	n/a
37	BACH1	chr11:93839944-93839957	K562	blood:	n/a	n/a
38	BACH1	chr11:93861448-93862639	H1-hESC	embryonic stem cell:	n/a	n/a
39	BACH1	chr11:93865234-93865434	K562	blood:	n/a	n/a
40	BACH1	chr11:93957221-93957507	H1-hESC	embryonic stem cell:	n/a	n/a
41	BACH1	chr11:93754699-93755013	K562	blood:	n/a	n/a
42	BACH1	chr11:93957208-93957365	K562	blood:	n/a	n/a
43	BACH1	chr11:93951679-93951681	H1-hESC	embryonic stem cell:	n/a	n/a
44	BCL3	chr11:93861678-93862220	A549	lung:	n/a	chr11:93861906-93861915 chr11:93862074-93862087 chr11:93862098-93862107
45	BCL3	chr11:93934100-93934604	A549	lung:	n/a	n/a
46	BCL3	chr11:93934188-93934548	A549	lung:	n/a	n/a
47	BCL3	chr11:93861593-93862215	A549	lung:	n/a	chr11:93861906-93861915 chr11:93862074-93862087 chr11:93862098-93862107
48	BCLAF1	chr11:93861428-93862271	GM12878	blood:	n/a	chr11:93861906-93861915 chr11:93862074-93862087 chr11:93862098-93862107
49	BCLAF1	chr11:93861670-93862633	GM12878	blood:	n/a	chr11:93861906-93861915 chr11:93862277-93862286 chr11:93862074-93862087 chr11:93862098-93862107
50	BHLHE40	chr11:93868276-93868540	K562	blood:	n/a	chr11:93868348-93868364

(count:3297 , 50 per page) page: 1 2 3 4 5 6 7 ... 66

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:93753348-93753398	PFSK-1	brain:	n/a
2	chr11:93822294-93822344	HAEpiC	amniotic membrane:	n/a
3	chr11:93860745-93860795	AG09319	gingival:	n/a
4	chr11:93753348-93753398	PFSK-1	brain:	n/a
5	chr11:93822294-93822344	HAEpiC	amniotic membrane:	n/a
6	chr11:93860745-93860795	AG09319	gingival:	n/a
7	chr11:93913200-93913250	NT2-D1	testis:	n/a
8	chr11:93885254-93885304	HRPEpiC	eye:	n/a
9	chr11:93822184-93822234	SK-N-MC	brain:	n/a
10	chr11:93824553-93824603	GM12891	blood:	n/a
11	chr11:93822184-93822234	NHDF-neo	bronchial:	n/a
12	chr11:93916953-93917003	GM12891	blood:	n/a
13	chr11:93927425-93927475	CMK	blood:	n/a
14	chr11:93824553-93824603	GM06990	blood:	n/a
15	chr11:93861779-93861829	SKMC	muscle:	n/a
16	chr11:93861779-93861829	HL-60	blood:	n/a
17	chr11:93895866-93895916	BE2_C	brain:	n/a
18	chr11:93867992-93868042	LNCaP	prostate:	n/a
19	chr11:93861779-93861829	IMR90	lung:	fetal
20	chr11:93862060-93862110	K562	blood:	n/a
21	chr11:93754223-93754273	GM19239	blood:	n/a
22	chr11:93885254-93885304	HRCEpiC	kidney:	n/a
23	chr11:93913200-93913250	T-47D	breast:	n/a
24	chr11:93927425-93927475	BJ	skin:	n/a
25	chr11:93822294-93822344	AG04450	lung:	fetal
26	chr11:93862073-93862123	HL-60	blood:	n/a
27	chr11:93822294-93822344	NB4	blood:	n/a
28	chr11:93862749-93862799	NHDF-neo	bronchial:	n/a
29	chr11:93861839-93861889	NB4	blood:	n/a
30	chr11:93865443-93865493	AoSMC	blood vessel:	n/a
31	chr11:93875999-93876049	CMK	blood:	n/a
32	chr11:93838695-93838745	GM12892	blood:	n/a
33	chr11:93922202-93922252	RPTEC	kidney:	n/a
34	chr11:93824553-93824603	HEEpiC	esophagus:	n/a
35	chr11:93907969-93908019	BE2_C	brain:	n/a
36	chr11:93874318-93874368	A549	lung:	n/a
37	chr11:93863858-93863908	AG09319	gingival:	n/a
38	chr11:93862516-93862566	HCF	heart:	n/a
39	chr11:93754094-93754144	HEK293	kidney:	embryo
40	chr11:93885254-93885304	HCM	heart:	n/a
41	chr11:93822022-93822072	HRPEpiC	eye:	n/a
42	chr11:93753348-93753398	GM12878	blood:	n/a
43	chr11:93885254-93885304	HCF	heart:	n/a
44	chr11:93861987-93862037	SAEC	small airway:	n/a
45	chr11:93753348-93753398	PANC-1	pancreas:	n/a
46	chr11:93846406-93846456	PFSK-1	brain:	n/a
47	chr11:93754288-93754338	HL-60	blood:	n/a
48	chr11:93914532-93914582	HAEpiC	amniotic membrane:	n/a
49	chr11:93907969-93908019	K562	blood:	n/a
50	chr11:93754390-93754440	HCT-116	colon:	n/a

(count:99 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr11:93843038..93846219-chr11:93861023..93863615,3	MCF-7	breast:
2	chr11:93834842..93837359-chr11:93842691..93845268,2	K562	blood:
3	chr11:93840966..93842950-chr11:93859232..93861067,2	K562	blood:
4	chr11:93928773..93931046-chr11:93935026..93936548,2	MCF-7	breast:
5	chr11:93783219..93786344-chr11:93787044..93789064,3	K562	blood:
6	chr11:93844146..93845919-chr11:93859116..93861491,2	K562	blood:
7	chr11:93932886..93934765-chr11:93936534..93938531,2	K562	blood:
8	chr11:93861273..93862040-chr8:141473868..141474564,2	Hela-S3	cervix:
9	chr11:93945976..93948199-chr11:93951746..93953756,2	K562	blood:
10	chr11:93874386..93876238-chr11:93877234..93879680,2	MCF-7	breast:
11	chr11:93916648..93917265-chr11:94150276..94150816,3	MCF-7	breast:
12	chr11:93899070..93901614-chr11:93903324..93905599,3	K562	blood:
13	chr11:93792129..93794478-chr11:93795523..93798448,3	K562	blood:
14	chr11:93904970..93905492-chr11:93917118..93917628,2	K562	blood:
15	chr11:93937398..93939250-chr11:93947688..93950358,2	K562	blood:
16	chr11:93914625..93916953-chr11:94227203..94228744,2	MCF-7	breast:
17	chr11:93929115..93931956-chr11:94225381..94228826,3	K562	blood:
18	chr11:93899070..93901930-chr11:93903657..93905599,2	K562	blood:
19	chr11:93860234..93863458-chr11:94225545..94228425,3	K562	blood:
20	chr11:93741108..93743362-chr11:93748550..93751276,2	K562	blood:
21	chr11:93867029..93870976-chr11:93873101..93877852,6	K562	blood:
22	chr11:93916747..93917349-chr11:94058220..94059212,2	MCF-7	breast:
23	chr11:93654234..93656516-chr11:93799480..93801603,2	K562	blood:
24	chr11:93880754..93883524-chr11:93885061..93886886,2	K562	blood:
25	chr11:93844204..93845981-chr11:93847595..93849691,2	MCF-7	breast:
26	chr11:93844146..93846103-chr11:93859991..93861903,2	K562	blood:
27	chr11:93862864..93865828-chr11:93884142..93886084,2	MCF-7	breast:
28	chr11:93834842..93837359-chr11:93842691..93845268,2	K562	blood:
29	chr11:93862864..93865828-chr11:93884142..93886084,2	MCF-7	breast:
30	chr11:93819657..93820474-chr20:61915385..61916068,2	MCF-7	breast:
31	chr11:93654636..93655438-chr11:93916836..93917602,2	MCF-7	breast:
32	chr11:93815540..93817373-chr11:93818109..93821051,2	K562	blood:
33	chr11:93867049..93869190-chr11:94275385..94277277,2	K562	blood:
34	chr11:93815540..93817373-chr11:93818109..93821051,2	K562	blood:
35	chr11:93861104..93863451-chr11:93914725..93916276,2	K562	blood:
36	chr11:93861895..93865118-chr11:93874866..93877940,3	K562	blood:
37	chr11:93867029..93870976-chr11:93873101..93877852,6	K562	blood:
38	chr11:93861143..93863415-chr11:93902863..93904604,2	MCF-7	breast:
39	chr11:93628291..93629247-chr11:93840284..93841220,3	MCF-7	breast:
40	chr11:93790115..93792446-chr11:93795397..93797125,2	K562	blood:
41	chr11:93860451..93862555-chr11:93865619..93868399,2	MCF-7	breast:
42	chr11:93835888..93838608-chr11:93905991..93908122,2	K562	blood:
43	chr11:93790115..93792446-chr11:93795397..93797125,2	K562	blood:
44	chr10:74385975..74386476-chr11:93840420..93840920,2	NB4	blood:
45	chr11:93875120..93879114-chr11:93880737..93884211,6	K562	blood:
46	chr11:93917086..93919356-chr11:93920990..93923600,2	K562	blood:
47	chr11:93741108..93743362-chr11:93748550..93751276,2	K562	blood:
48	chr11:93907084..93908799-chr11:93910378..93911922,2	K562	blood:
49	chr11:93866030..93868662-chr11:93884389..93887583,3	K562	blood:
50	chr11:93861478..93862275-chr16:56642270..56643142,2	Hela-S3	cervix:

(count:8 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GPR83-2	chr11:93932428-93932509	NONHSAT023709
2	lnc-GPR83-2	chr11:93932661-93932887	NONHSAT023709
3	lnc-VSTM5-3	chr11:93760135-93761825	NONHSAT023702
4	lnc-GPR83-5	chr11:93921615-93922163	NONHSAT023708
5	lnc-PANX1-1	chr11:93935412-93935672	NONHSAT023711
6	lnc-GPR83-2	chr11:93932662-93932887	XLOC_009524
7	lnc-HEPHL1-1	chr11:93851046-93851433	NONHSAT023705
8	lnc-GPR83-2	chr11:93932429-93932509	XLOC_009524

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location
1	PANX1	hsa-miR-10a-5p	chr11:93914431-93914453
2	PANX1	hsa-miR-125a-5p	chr11:93914428-93914452
3	PANX1	hsa-miR-16-5p	chr11:93914663-93914684

Variant related genes	Relation type
ENSG00000227593	TF binding region
ENSG00000250519	TF binding region
ENSG00000256745	TF binding region
HEPHL1	TF binding region
PANX1	TF binding region
ENSG00000227593	CpG island
ENSG00000250519	CpG island
ENSG00000256745	CpG island
HEPHL1	CpG island
PANX1	CpG island
ENSG00000125148	chromatin interactions
ENSG00000020922	chromatin interactions
ENSG00000110218	chromatin interactions
ENSG00000171843	chromatin interactions
ENSG00000168876	chromatin interactions
ENSG00000197747	chromatin interactions
ENSG00000255995	chromatin interactions
ENSG00000101199	chromatin interactions
ENSG00000256745	chromatin interactions
ENSG00000181333	chromatin interactions
ENSG00000188825	chromatin interactions
ENSG00000196371	chromatin interactions
ENSG00000134627	chromatin interactions
ENSG00000263966	chromatin interactions

Extended variants
information (count: 7917 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:7917 , 50 per page) page: 1 2 3 4 5 6 7 ... 159

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs959343	chr11:93741612-93741613	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs72966603	chr11:93741621-93741622	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
3	rs558599861	chr11:93741645-93741646	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs959342	chr11:93741653-93741654	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
5	rs538141418	chr11:93741661-93741662	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs556419385	chr11:93741666-93741667	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs113401937	chr11:93741753-93741754	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs182753843	chr11:93741755-93741756	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs55960599	chr11:93741758-93741759	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs368264014	chr11:93741803-93741804	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs545860806	chr11:93741816-93741817	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs564141231	chr11:93741967-93741968	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs188995879	chr11:93741993-93741994	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs550098645	chr11:93742002-93742003	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs575391890	chr11:93742031-93742032	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs544467005	chr11:93742032-93742033	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs529490539	chr11:93742039-93742040	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs547990681	chr11:93742096-93742097	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs564280561	chr11:93742135-93742136	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs566106238	chr11:93742163-93742164	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs577863792	chr11:93742206-93742207	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs533882125	chr11:93742232-93742233	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs193129695	chr11:93742236-93742237	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs570509891	chr11:93742237-93742238	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs372217498	chr11:93742241-93742242	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs908752	chr11:93742265-93742266	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs185776824	chr11:93742282-93742283	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs188946488	chr11:93742310-93742311	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs563764672	chr11:93742327-93742328	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs67708140	chr11:93742328-93742329	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs75132937	chr11:93742341-93742342	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs538266277	chr11:93742418-93742419	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs553951129	chr11:93742437-93742438	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs76244898	chr11:93742533-93742534	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs545936736	chr11:93742560-93742561	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs2460070	chr11:93742614-93742615	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs11020626	chr11:93742636-93742637	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs543776398	chr11:93742720-93742721	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs561904892	chr11:93742772-93742773	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs529604937	chr11:93742785-93742786	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs78960850	chr11:93742793-93742794	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs140920968	chr11:93742807-93742808	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs573199439	chr11:93742818-93742819	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs192206938	chr11:93742833-93742834	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs371855473	chr11:93742842-93742843	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs183989356	chr11:93742856-93742857	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs552343783	chr11:93742918-93742919	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs2511382	chr11:93742989-93742990	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
49	rs531365155	chr11:93742993-93742994	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs549771279	chr11:93743007-93743008	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:95)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Wilms tumour	21544195	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Acute myeloid leukemia	20729466	CNVD
Cancer	21637783	CNVD
Acute myeloid leukemia	16864856	CNVD
Chronic lymphocytic leukemia	21795749	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21484798	CNVD
Ewing''s sarcoma	21437220	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	20837533	CNVD
Breast cancer	21264507	CNVD
Cervical cancer	21063398	CNVD
Glioblastoma multiforme	19960244	CNVD
Liposarcoma	21253554	CNVD
Neuroblastoma	18923524	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Neuroblastoma	17533364	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Cervical cancer	21062161	CNVD
Esophageal squamous carcinoma	18350619	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	22429812	CNVD
Breast cancer	16608533	CNVD
T-cell lymphomas	19863542	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Basal cell lymphoma	17053054	CNVD
Hepatocellular carcinoma	16785998	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21785460	CNVD
Cancer	22183965	CNVD
Melanoma	22183965	CNVD
Developmental delay	21147756	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21958427	CNVD
Lung cancer	18438408	CNVD
Ewing''s sarcoma	17952124	CNVD
Renal cell carcinoma	18194544	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	17133270	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Ductal carcinoma	22052326	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
Mental retardation	21062444	CNVD
Cancer	21499728	CNVD
Breast cancer	19181860	CNVD
Breast cancer	17603634	CNVD
Mantle cell lymphoma	19029149	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Basal cell lymphoma	16790693	CNVD
Breast cancer	21509527	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	18852474	CNVD
Cancer	20164919	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Breast cancer	22844521	CNVD
DNA damage stimulus	22844521	CNVD
DNA repair	22844521	CNVD
Ovarian cancer	22844521	CNVD
Prostate cancer	22844521	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:3513 , 50 per page) page: 1 2 3 4 5 6 7 ... 71

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:93740600-93742000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
2	chr11:93740600-93745800	Enhancers	NHEK	skin
3	chr11:93740600-93746000	Enhancers	HMEC	breast
4	chr11:93740800-93741800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr11:93740800-93746000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
6	chr11:93741200-93741800	Enhancers	Esophagus	oesophagus
7	chr11:93741800-93742800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr11:93741800-93742800	Weak transcription	Esophagus	oesophagus
9	chr11:93742000-93743000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
10	chr11:93742800-93743800	Enhancers	Esophagus	oesophagus
11	chr11:93742800-93745800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr11:93743000-93745400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
13	chr11:93745800-93747000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr11:93746000-93749600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
15	chr11:93747000-93747800	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
16	chr11:93747800-93750400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
17	chr11:93749600-93754200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
18	chr11:93749600-93754400	Enhancers	HMEC	breast
19	chr11:93750200-93753800	Enhancers	NHEK	skin
20	chr11:93750400-93754800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
21	chr11:93750800-93752200	Enhancers	NH-A	brain
22	chr11:93751000-93754200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr11:93752200-93752400	Enhancers	Breast Myoepithelial Primary Cells	Breast
24	chr11:93752200-93758000	Weak transcription	NH-A	brain
25	chr11:93753400-93753800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
26	chr11:93753800-93755800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
27	chr11:93753800-93756200	Flanking Active TSS	NHEK	skin
28	chr11:93754000-93756200	Enhancers	Breast Myoepithelial Primary Cells	Breast
29	chr11:93754200-93754800	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
30	chr11:93754200-93754800	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
31	chr11:93754200-93754800	Enhancers	Aorta	Aorta
32	chr11:93754400-93754800	Enhancers	H1 Cell Line	embryonic stem cell
33	chr11:93754400-93756200	Flanking Active TSS	HMEC	breast
34	chr11:93754800-93755000	Flanking Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
35	chr11:93754800-93755000	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
36	chr11:93754800-93755200	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
37	chr11:93754800-93755400	Weak transcription	Aorta	Aorta
38	chr11:93755000-93755200	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
39	chr11:93755000-93757400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
40	chr11:93755200-93756000	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
41	chr11:93755200-93756200	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
42	chr11:93755400-93755600	Enhancers	Aorta	Aorta
43	chr11:93755400-93755600	Enhancers	Placenta Amnion	Placenta Amnion
44	chr11:93755600-93760600	Weak transcription	Placenta Amnion	Placenta Amnion
45	chr11:93755800-93761200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
46	chr11:93756000-93756600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
47	chr11:93756200-93756800	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
48	chr11:93756200-93757000	Enhancers	NHEK	skin
49	chr11:93756200-93759000	Enhancers	HMEC	breast
50	chr11:93756600-93758000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin

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