Variant report

Variant	nsv530903
Chromosome Location	chr9:52389-356138
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3123)
CpG islands
(count:1832)
Chromatin interactive
region (count:135)
LncRNA
region (count:46)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:3123 , 50 per page) page: 1 2 3 4 5 6 7 ... 63

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:95057-95158	K562	blood:	n/a	n/a
2	ARID3A	chr9:267916-268404	K562	blood:	n/a	n/a
3	ARID3A	chr9:238911-239096	K562	blood:	n/a	n/a
4	ARID3A	chr9:237608-238477	K562	blood:	n/a	n/a
5	ARID3A	chr9:94438-94633	K562	blood:	n/a	chr9:94582-94598
6	ARID3A	chr9:336046-336405	HepG2	liver:	n/a	n/a
7	ARID3A	chr9:272758-273406	K562	blood:	n/a	chr9:273064-273079
8	ARID3A	chr9:250210-251866	K562	blood:	n/a	n/a
9	ARID3A	chr9:210220-210873	K562	blood:	n/a	n/a
10	ARID3A	chr9:215966-216247	K562	blood:	n/a	n/a
11	ARID3A	chr9:229136-229466	K562	blood:	n/a	n/a
12	ARID3A	chr9:214214-215154	K562	blood:	n/a	n/a
13	ARID3A	chr9:272095-272522	K562	blood:	n/a	n/a
14	ARID3A	chr9:260270-260544	K562	blood:	n/a	n/a
15	ATF1	chr9:94435-94576	K562	blood:	n/a	n/a
16	ATF1	chr9:272781-273161	K562	blood:	n/a	n/a
17	ATF1	chr9:222266-222777	K562	blood:	n/a	n/a
18	ATF1	chr9:249153-249485	K562	blood:	n/a	n/a
19	ATF1	chr9:312958-313372	K562	blood:	n/a	n/a
20	ATF1	chr9:272150-272512	K562	blood:	n/a	n/a
21	ATF1	chr9:270753-271026	K562	blood:	n/a	n/a
22	ATF1	chr9:211078-211816	K562	blood:	n/a	n/a
23	ATF2	chr9:272650-273286	GM12878	blood:	n/a	n/a
24	ATF2	chr9:272677-273240	GM12878	blood:	n/a	n/a
25	ATF2	chr9:297286-297859	GM12878	blood:	n/a	n/a
26	ATF3	chr9:210212-210461	K562	blood:	n/a	n/a
27	ATF3	chr9:326568-327022	H1-hESC	embryonic stem cell:	n/a	n/a
28	ATF3	chr9:272081-272576	K562	blood:	n/a	n/a
29	BACH1	chr9:207498-207603	K562	blood:	n/a	n/a
30	BACH1	chr9:214910-215270	H1-hESC	embryonic stem cell:	n/a	n/a
31	BACH1	chr9:63102-63125	H1-hESC	embryonic stem cell:	n/a	n/a
32	BACH1	chr9:214677-214706	H1-hESC	embryonic stem cell:	n/a	n/a
33	BACH1	chr9:113631-113796	H1-hESC	embryonic stem cell:	n/a	n/a
34	BACH1	chr9:114203-114262	H1-hESC	embryonic stem cell:	n/a	n/a
35	BATF	chr9:156926-157447	GM12878	blood:	n/a	n/a
36	BATF	chr9:156635-156839	GM12878	blood:	n/a	n/a
37	BATF	chr9:156608-156841	GM12878	blood:	n/a	n/a
38	BATF	chr9:88649-88891	GM12878	blood:	n/a	chr9:88843-88853 chr9:88842-88853
39	BATF	chr9:199669-200113	GM12878	blood:	n/a	n/a
40	BATF	chr9:198874-199092	GM12878	blood:	n/a	chr9:198886-198895
41	BATF	chr9:88665-89067	GM12878	blood:	n/a	chr9:88843-88853 chr9:88842-88853
42	BATF	chr9:184237-185449	GM12878	blood:	n/a	chr9:184501-184509
43	BATF	chr9:167629-168111	GM12878	blood:	n/a	n/a
44	BATF	chr9:198812-199262	GM12878	blood:	n/a	chr9:198886-198895
45	BATF	chr9:178645-179348	GM12878	blood:	n/a	chr9:179069-179082
46	BATF	chr9:185181-185422	GM12878	blood:	n/a	n/a
47	BATF	chr9:122820-123095	GM12878	blood:	n/a	n/a
48	BATF	chr9:156921-157465	GM12878	blood:	n/a	n/a
49	BATF	chr9:194727-194900	GM12878	blood:	n/a	n/a
50	BATF	chr9:116510-116717	GM12878	blood:	n/a	n/a

(count:1832 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:117044-117094	NHDF-neo	bronchial:	n/a
2	chr9:214690-214740	U87	brain:	n/a
3	chr9:117044-117094	NHDF-neo	bronchial:	n/a
4	chr9:214690-214740	U87	brain:	n/a
5	chr9:213650-213700	Caco-2	colon:	n/a
6	chr9:72961-73011	IMR90	lung:	fetal
7	chr9:73835-73885	PANC-1	pancreas:	n/a
8	chr9:114838-114888	ovcar-3	ovarian:	n/a
9	chr9:214268-214318	T-47D	breast:	n/a
10	chr9:117608-117658	HRE	kidney:	n/a
11	chr9:214268-214318	AoSMC	blood vessel:	n/a
12	chr9:117608-117658	HepG2	liver:	n/a
13	chr9:117608-117658	CMK	blood:	n/a
14	chr9:72908-72958	HAEpiC	amniotic membrane:	n/a
15	chr9:72961-73011	Caco-2	colon:	n/a
16	chr9:215368-215418	HCPEpiC	choroid plexus:	n/a
17	chr9:214612-214662	PANC-1	pancreas:	n/a
18	chr9:73704-73754	NHBE	bronchial:	n/a
19	chr9:113530-113580	HEEpiC	esophagus:	n/a
20	chr9:73835-73885	HMEC	breast:	n/a
21	chr9:214612-214662	GM12891	blood:	n/a
22	chr9:114434-114484	GM06990	blood:	n/a
23	chr9:176893-176943	HEEpiC	esophagus:	n/a
24	chr9:117608-117658	PFSK-1	brain:	n/a
25	chr9:72908-72958	GM06990	blood:	n/a
26	chr9:113530-113580	HEK293	kidney:	embryo
27	chr9:112937-112987	Caco-2	colon:	n/a
28	chr9:73704-73754	Hepatocyte	liver:	n/a
29	chr9:112937-112987	HPAEpiC	pulmonary alveolar:	n/a
30	chr9:118091-118141	HRPEpiC	eye:	n/a
31	chr9:117608-117658	T-47D	breast:	n/a
32	chr9:215561-215611	ProgFib	skin:	n/a
33	chr9:176893-176943	ovcar-3	ovarian:	n/a
34	chr9:114140-114190	PFSK-1	brain:	n/a
35	chr9:117608-117658	SK-N-SH	brain:	n/a
36	chr9:112618-112668	HEK293	kidney:	embryo
37	chr9:113530-113580	CMK	blood:	n/a
38	chr9:168828-168878	BJ	skin:	n/a
39	chr9:215561-215611	HCF	heart:	n/a
40	chr9:117044-117094	Hepatocyte	liver:	n/a
41	chr9:73568-73618	NHDF-neo	bronchial:	n/a
42	chr9:109039-109089	SK-N-SH_RA	brain:	n/a
43	chr9:211689-211739	AG09309	skin:	n/a
44	chr9:114140-114190	MCF10A-Er-Src	breast:	n/a
45	chr9:215368-215418	SK-N-MC	brain:	n/a
46	chr9:112618-112668	RPTEC	kidney:	n/a
47	chr9:118698-118748	HPAEpiC	pulmonary alveolar:	n/a
48	chr9:214268-214318	HL-60	blood:	n/a
49	chr9:117044-117094	AoSMC	blood vessel:	n/a
50	chr9:114140-114190	HEEpiC	esophagus:	n/a

(count:135 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr9:214778..216543-chr9:219574..221163,2	MCF-7	breast:
2	chr9:276314..278461-chr9:285139..287718,2	K562	blood:
3	chr9:210795..213326-chr9:213922..216378,4	MCF-7	breast:
4	chr9:237104..239333-chr9:240417..242425,2	K562	blood:
5	chr9:214682..216322-chr9:293864..296795,2	MCF-7	breast:
6	chr9:324085..328451-chr9:329787..332698,3	K562	blood:
7	chr9:207956..209819-chr9:211466..213662,2	MCF-7	breast:
8	chr9:207871..210695-chr9:212521..216858,5	MCF-7	breast:
9	chr9:224153..226474-chr9:270248..273178,2	K562	blood:
10	chr9:213587..215367-chr9:247326..250011,2	MCF-7	breast:
11	chr9:217275..219531-chr9:301975..303827,2	MCF-7	breast:
12	chr9:318530..320927-chr9:322721..325349,2	K562	blood:
13	chr9:250806..252981-chr9:269858..272236,2	MCF-7	breast:
14	chr9:247322..249745-chr9:277912..279940,2	K562	blood:
15	chr9:218197..221460-chr9:224650..228237,4	K562	blood:
16	chr9:210056..211721-chr9:271493..274380,2	K562	blood:
17	chr9:286841..289218-chr9:291668..294143,2	K562	blood:
18	chr9:239328..240900-chr9:247584..249872,2	K562	blood:
19	chr9:303334..306488-chr9:313112..315414,3	MCF-7	breast:
20	chr9:213589..216422-chr9:270983..274599,7	K562	blood:
21	chr9:288330..291260-chr9:302503..304653,3	K562	blood:
22	chr9:303334..306488-chr9:313112..315414,3	MCF-7	breast:
23	chr9:246962..249799-chr9:250077..252857,2	K562	blood:
24	chr9:286841..289218-chr9:291668..294143,2	K562	blood:
25	chr9:212545..218648-chr9:270340..281940,20	K562	blood:
26	chr9:275975..278627-chr9:279451..282123,3	K562	blood:
27	chr9:211790..213319-chr9:241598..244495,2	K562	blood:
28	chr9:255761..258409-chr9:263285..266102,2	K562	blood:
29	chr9:261493..264345-chr9:269680..272564,2	MCF-7	breast:
30	chr9:214285..216173-chr9:227690..229444,2	K562	blood:
31	chr9:211063..213249-chr9:216572..219831,3	K562	blood:
32	chr9:227507..229537-chr9:238867..240547,2	K562	blood:
33	chr9:213452..215018-chr9:305580..307976,2	K562	blood:
34	chr9:235818..237375-chr9:247234..248835,2	K562	blood:
35	chr9:237104..239333-chr9:240417..242425,2	K562	blood:
36	chr9:276314..278461-chr9:285139..287718,2	K562	blood:
37	chr9:258428..261727-chr9:265742..268870,3	K562	blood:
38	chr9:211395..217021-chr9:276782..283147,8	K562	blood:
39	chr9:216842..219174-chr9:220888..224256,4	K562	blood:
40	chr9:223210..226112-chr9:277917..282090,3	K562	blood:
41	chr9:213518..215162-chr9:305580..308186,2	K562	blood:
42	chr9:207715..211592-chr9:270281..275557,5	K562	blood:
43	chr9:257830..262248-chr9:271354..273884,5	K562	blood:
44	chr9:350965..353575-chr9:397923..399924,2	K562	blood:
45	chr9:226722..229215-chr9:247840..250679,2	K562	blood:
46	chr9:213868..216890-chr9:248711..251891,4	K562	blood:
47	chr9:283346..286966-chr9:287946..290894,7	K562	blood:
48	chr9:252242..255061-chr9:271559..273805,3	K562	blood:
49	chr9:264854..268401-chr9:271602..276392,5	K562	blood:
50	chr9:224171..226015-chr9:253370..255238,2	MCF-7	breast:

(count:46 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FOXD4-4	chr9:92740-92941	NONHSAT129893
2	lnc-DOCK8-6	chr9:78742-78826	NONHSAT129886
3	lnc-FOXD4-4	chr9:90995-91304	ucscGeneNc_uc003zfy_2
4	lnc-DOCK8-3	chr9:74882-75298	ENSG00000225655.1
5	lnc-FOXD4-2	chr9:102473-102541	ENSG00000227917
6	lnc-FOXD4-3	chr9:113606-113656	NONHSAT129899
7	lnc-FOXD4-2	chr9:102740-102850	NONHSAT129895
8	lnc-DOCK8-6	chr9:64149-64205	NONHSAT129888
9	lnc-FOXD4-2	chr9:102716-103067	NONHSAT129896
10	lnc-DOCK8-3	chr9:79345-79537	ENSG00000225655.1
11	lnc-FOXD4-2	chr9:103694-103754	NONHSAT129896
12	lnc-FOXD4-4	chr9:92740-92850	NONHSAT129892
13	lnc-FOXD4-2	chr9:101014-101304	NONHSAT129895
14	lnc-FOXD4-1	chr9:112716-113067	ENSG00000231808
15	lnc-FOXD4-4	chr9:90804-91304	NONHSAT129892
16	lnc-FOXD4-2	chr9:101002-101304	ENSG00000227917
17	lnc-FOXD4-2	chr9:102740-102941	ENSG00000227917
18	lnc-C9orf66-1	chr9:267966-268273	ENSG00000235880.1
19	lnc-DOCK8-6	chr9:62706-62816	NONHSAT129887
20	lnc-DOCK8-6	chr9:64882-65298	NONHSAT129888
21	lnc-DOCK8-6	chr9:62698-62816	ucscGeneNc_uc003zfx_2
22	lnc-DOCK8-6	chr9:64882-65292	ucscGeneNc_uc003zfx_2
23	lnc-DOCK8-3	chr9:72716-72816	ENSG00000225655.1
24	lnc-FOXD4-4	chr9:91002-91304	NONHSAT129893
25	lnc-FOXD4-1	chr9:113694-113754	ENSG00000231808
26	lnc-FOXD4-2	chr9:108804-109469	NONHSAT129897
27	lnc-FOXD4-5	chr9:151745-152078	NONHSAT129910
28	lnc-FOXD4-2	chr9:109596-109842	NONHSAT129897
29	lnc-DOCK8-6	chr9:64882-65298	NONHSAT129887
30	lnc-FOXD4-5	chr9:156481-156527	NONHSAT129910
31	lnc-DOCK8-3	chr9:74882-75298	ENSG00000225655.1
32	lnc-FOXD4-2	chr9:109316-109471	NONHSAT129895
33	lnc-DOCK8-6	chr9:69345-69537	NONHSAT129886
34	lnc-FOXD4-4	chr9:92473-92541	NONHSAT129893
35	lnc-DOCK8-6	chr9:62716-62816	NONHSAT129888
36	lnc-FOXD4-3	chr9:114040-115772	NONHSAT129899
37	lnc-FOXD4-5	chr9:154709-154795	NONHSAT129910
38	lnc-FOXD4-4	chr9:92473-92541	ucscGeneNc_uc003zfy_2
39	lnc-DOCK8-6	chr9:62701-62816	NONHSAT129886
40	lnc-C9orf66-1	chr9:272905-273002	ENSG00000235880.1
41	lnc-FOXD4-4	chr9:92740-92941	ucscGeneNc_uc003zfy_2
42	lnc-FOXD4-5	chr9:161567-161647	NONHSAT129910
43	lnc-DOCK8-3	chr9:88742-88826	ENSG00000225655.1
44	lnc-DOCK8-3	chr9:72706-72816	ENSG00000225655.1
45	lnc-DOCK8-3	chr9:72701-72816	ENSG00000225655.1
46	lnc-DOCK8-3	chr9:74149-74205	ENSG00000225655.1

No data

Variant related genes	Relation type
DOCK8	TF binding region
ENSG00000231808	TF binding region
ENSG00000225655	TF binding region
FOXD4	TF binding region
ENSG00000235880	TF binding region
ENSG00000144140	TF binding region
ENSG00000227917	TF binding region
CBWD1	TF binding region
C9orf66	TF binding region
DOCK8	CpG island
ENSG00000231808	CpG island
ENSG00000225655	CpG island
FOXD4	CpG island
ENSG00000235880	CpG island
ENSG00000144140	CpG island
ENSG00000227917	CpG island
CBWD1	CpG island
C9orf66	CpG island
ENSG00000107099	chromatin interactions
ENSG00000235880	chromatin interactions
ENSG00000227155	chromatin interactions
ENSG00000101191	chromatin interactions
ENSG00000183784	chromatin interactions

Extended variants
information (count: 11968 )
Associated
traits (count: 123 )

Variant overlapped rSNPs/rCNVs (count:11968 , 50 per page) page: 1 2 3 4 5 6 7 ... 240

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs534061989	chr9:52392-52393	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs2441639	chr9:52415-52416	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs574123695	chr9:52420-52421	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs544614105	chr9:52432-52433	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs556499842	chr9:52457-52458	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs577968109	chr9:52462-52463	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs201719601	chr9:52479-52480	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs199952527	chr9:52481-52482	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs200692447	chr9:52492-52493	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs560059569	chr9:52505-52506	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs527458041	chr9:52538-52539	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs542388836	chr9:52585-52586	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs149992177	chr9:52625-52626	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs565750972	chr9:52626-52627	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs560650526	chr9:52649-52650	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs62531212	chr9:52652-52653	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs531213338	chr9:52658-52659	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs549328347	chr9:52689-52690	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs569226549	chr9:52718-52719	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs533432282	chr9:52745-52746	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs552030589	chr9:52764-52765	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs62531213	chr9:52789-52790	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs371450543	chr9:52877-52878	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs148102682	chr9:52886-52887	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs555627495	chr9:52896-52897	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs567715180	chr9:52927-52928	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs200462581	chr9:52954-52955	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs538252375	chr9:52957-52958	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs9407282	chr9:52963-52964	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs556561330	chr9:53201-53202	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs576097314	chr9:53300-53301	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs2259286	chr9:53314-53315	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs9408583	chr9:53335-53336	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs578013761	chr9:53346-53347	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs545001349	chr9:53356-53357	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs374103489	chr9:53361-53362	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs554016798	chr9:53391-53392	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs547356351	chr9:62003-62004	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs559244949	chr9:62035-62036	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs547263975	chr9:62118-62119	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs529966325	chr9:62119-62120	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs548066307	chr9:62130-62131	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs565589393	chr9:62133-62134	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs149267085	chr9:62154-62155	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs536849028	chr9:62190-62191	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs552251927	chr9:62234-62235	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs9408614	chr9:62261-62262	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs570410895	chr9:62288-62289	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs534616988	chr9:62315-62316	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs551222995	chr9:62360-62361	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:123)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	20164920	CNVD
Ovarian cancer	21720365	CNVD
Myelofibrosis	22110671	CNVD
Lynch syndrome	18415027	CNVD
Retinoblastoma	21504564	CNVD
Melanoma	18172304	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Glioblastoma multiforme	22286061	CNVD
Williams-beuren syndrome	18553513	CNVD
Disorders of sex development	21048976	CNVD
Pilocytic astrocytoma	18622384	CNVD
Pilomyxoid astrocytoma	18622384	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
prenatal diagnosis	20453657	CNVD
Gastric cancer	16715143	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Intracranial aneurysm	16715129	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Disorders of sex development	22290220	CNVD
Glioblastoma multiforme	21080181	CNVD
Sudden cardiac death	19188705	CNVD
Non-small cell lung cancer	21829676	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21183584	CNVD
Non-small cell lung cancer	21952639	CNVD
Neuroblastoma	18923191	CNVD
Intellectual disability	22102821	CNVD
abnormal development	18461090	CNVD
Honadal dysgenesis	21048976	CNVD
Medulloblastoma	21979893	CNVD
Lung cancer	16740712	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Breast cancer	16608533	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	16272173	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	17133270	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Cervical cancer	21063398	CNVD
Retinoblastoma	22278416	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Biliary cancer	19435499	CNVD
Gastric cancer	21586687	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myopathy	18421352	CNVD
Neuroblastoma	18664255	CNVD
Acute lymphoblastic leukemia	18957548	CNVD
Myeloproliferative neoplasm	17564968	CNVD
Malignant meningioma	17937814	CNVD
Glioma	21971842	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	17603634	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oligodendroglial tumors	17285580	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chordoma	21602918	CNVD
Renal cell carcinoma	18592004	CNVD
Developmental delay	19490664	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
microdeletion syndrome	16199537	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Cancer	20164919	CNVD
Chronic myeloid leukemia	21384125	CNVD
Autism	22495311	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
small cell lung cancer	20016488	CNVD
Developmental delay	21147756	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
early-passage human iPS cells	21368824	CNVD
Schizophrenia	20967226	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Schizophrenia	23813976	CNVD
Lung cancer	18438408	CNVD
Autism	20531469	CNVD
Breast cancer	22522925	CNVD
Intracranial ependymoma	16609018	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD
XY gonadal dysgenesis	20685758	CNVD
Urothelial carcinoma	21177765	CNVD
Oral cancer	21386901	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Developmental delay	20808231	CNVD
Obesity	20808231	CNVD
Myelodysplastic syndrome	21251322	CNVD
Primary immunodeficiency	22942019	CNVD
Melanoma	20877625	CNVD
Breast cancer	21785460	CNVD
Prostate cancer	18632612	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Cancer	21215367	CNVD
Renal cell carcinoma	21215367	CNVD
Williams Syndrome	20824207	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Pancreatic cancer	17952125	CNVD
T-cell lymphomas	22341440	CNVD
Breast cancer	21364760	CNVD
Bipolar disorder	19114987	CNVD
Breast cancer	21858162	CNVD
Renal cell carcinoma	21668985	CNVD

Chromatin state (count:3239 , 50 per page) page: 1 2 3 4 5 6 7 ... 65

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:48400-52400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
2	chr9:52400-53400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr9:52600-53000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
4	chr9:62000-62200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr9:62200-63000	Enhancers	Fetal Thymus	thymus
6	chr9:62800-63000	Enhancers	Dnd41	blood
7	chr9:63000-63200	Enhancers	Primary T helper cells PMA-I stimulated	--
8	chr9:63000-63200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
9	chr9:63000-63200	Flanking Active TSS	Fetal Thymus	thymus
10	chr9:63000-63200	Flanking Active TSS	Dnd41	blood
11	chr9:63000-63400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
12	chr9:63000-63400	Enhancers	Primary monocytes fromperipheralblood	blood
13	chr9:63000-63400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
14	chr9:63000-63600	Enhancers	Primary T cells fromperipheralblood	blood
15	chr9:63000-63600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
16	chr9:63000-63600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
17	chr9:63000-63600	Enhancers	Fetal Lung	lung
18	chr9:63000-64000	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
19	chr9:63000-64200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
20	chr9:63200-63400	Enhancers	Primary hematopoietic stem cells short term culture	blood
21	chr9:63200-63400	Active TSS	Fetal Thymus	thymus
22	chr9:63200-64000	Active TSS	Dnd41	blood
23	chr9:63600-65800	Weak transcription	Fetal Lung	lung
24	chr9:64000-64200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr9:64000-64200	Flanking Active TSS	Dnd41	blood
26	chr9:64200-64800	Enhancers	Dnd41	blood
27	chr9:65800-66000	Enhancers	Fetal Lung	lung
28	chr9:72200-74000	Active TSS	NHLF	lung
29	chr9:72600-73000	Bivalent/Poised TSS	Fetal Muscle Trunk	muscle
30	chr9:72800-73000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
31	chr9:72800-73000	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
32	chr9:72800-73000	Enhancers	Primary hematopoietic stem cells	blood
33	chr9:72800-73000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
34	chr9:72800-73000	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin01	Skin
35	chr9:72800-73000	Flanking Bivalent TSS/Enh	Foreskin Keratinocyte Primary Cells skin03	Skin
36	chr9:72800-73000	Flanking Bivalent TSS/Enh	Fetal Adrenal Gland	Adrenal Gland
37	chr9:72800-73000	Bivalent Enhancer	Fetal Thymus	thymus
38	chr9:72800-73000	Enhancers	Gastric	stomach
39	chr9:72800-73000	Bivalent Enhancer	Placenta Amnion	Placenta Amnion
40	chr9:72800-73000	Active TSS	Stomach Smooth Muscle	stomach
41	chr9:72800-73000	Enhancers	Spleen	Spleen
42	chr9:72800-73000	Bivalent Enhancer	Monocytes-CD14+_RO01746	blood
43	chr9:72800-73200	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
44	chr9:72800-73200	Bivalent Enhancer	Primary T cells effector/memory enriched fromperipheralblood	blood
45	chr9:72800-73600	Active TSS	Primary T regulatory cells fromperipheralblood	blood
46	chr9:72800-73600	Active TSS	Adipose Nuclei	Adipose
47	chr9:72800-73600	Active TSS	Skeletal Muscle Female	skeletal muscle
48	chr9:72800-73800	Bivalent/Poised TSS	ES-WA7 Cell Line	embryonic stem cell
49	chr9:72800-74000	Bivalent/Poised TSS	H1 Cell Line	embryonic stem cell
50	chr9:72800-74000	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell

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