Variant report

Variant	nsv8403
Chromosome Location	chr9:62805-324255
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2784)
CpG islands
(count:1833)
Chromatin interactive
region (count:122)
LncRNA
region (count:46)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2784 , 50 per page) page: 1 2 3 4 5 6 7 ... 56

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:215966-216247	K562	blood:	n/a	n/a
2	ARID3A	chr9:238911-239096	K562	blood:	n/a	n/a
3	ARID3A	chr9:260270-260544	K562	blood:	n/a	n/a
4	ARID3A	chr9:214214-215154	K562	blood:	n/a	n/a
5	ARID3A	chr9:94438-94633	K562	blood:	n/a	chr9:94582-94598
6	ARID3A	chr9:229136-229466	K562	blood:	n/a	n/a
7	ARID3A	chr9:210220-210873	K562	blood:	n/a	n/a
8	ARID3A	chr9:267916-268404	K562	blood:	n/a	n/a
9	ARID3A	chr9:272095-272522	K562	blood:	n/a	n/a
10	ARID3A	chr9:95057-95158	K562	blood:	n/a	n/a
11	ARID3A	chr9:237608-238477	K562	blood:	n/a	n/a
12	ARID3A	chr9:250210-251866	K562	blood:	n/a	n/a
13	ARID3A	chr9:272758-273406	K562	blood:	n/a	chr9:273064-273079
14	ATF1	chr9:211078-211816	K562	blood:	n/a	n/a
15	ATF1	chr9:94435-94576	K562	blood:	n/a	n/a
16	ATF1	chr9:312958-313372	K562	blood:	n/a	n/a
17	ATF1	chr9:270753-271026	K562	blood:	n/a	n/a
18	ATF1	chr9:272150-272512	K562	blood:	n/a	n/a
19	ATF1	chr9:249153-249485	K562	blood:	n/a	n/a
20	ATF1	chr9:222266-222777	K562	blood:	n/a	n/a
21	ATF1	chr9:272781-273161	K562	blood:	n/a	n/a
22	ATF2	chr9:272677-273240	GM12878	blood:	n/a	n/a
23	ATF2	chr9:272650-273286	GM12878	blood:	n/a	n/a
24	ATF2	chr9:297286-297859	GM12878	blood:	n/a	n/a
25	ATF3	chr9:210212-210461	K562	blood:	n/a	n/a
26	ATF3	chr9:272081-272576	K562	blood:	n/a	n/a
27	BACH1	chr9:114203-114262	H1-hESC	embryonic stem cell:	n/a	n/a
28	BACH1	chr9:207498-207603	K562	blood:	n/a	n/a
29	BACH1	chr9:63102-63125	H1-hESC	embryonic stem cell:	n/a	n/a
30	BACH1	chr9:113631-113796	H1-hESC	embryonic stem cell:	n/a	n/a
31	BACH1	chr9:214910-215270	H1-hESC	embryonic stem cell:	n/a	n/a
32	BACH1	chr9:214677-214706	H1-hESC	embryonic stem cell:	n/a	n/a
33	BATF	chr9:178036-178376	GM12878	blood:	n/a	n/a
34	BATF	chr9:74615-74984	GM12878	blood:	n/a	n/a
35	BATF	chr9:116510-116717	GM12878	blood:	n/a	n/a
36	BATF	chr9:278668-278987	GM12878	blood:	n/a	n/a
37	BATF	chr9:177184-177383	GM12878	blood:	n/a	n/a
38	BATF	chr9:167541-168102	GM12878	blood:	n/a	n/a
39	BATF	chr9:198874-199092	GM12878	blood:	n/a	chr9:198886-198895
40	BATF	chr9:185181-185422	GM12878	blood:	n/a	n/a
41	BATF	chr9:63237-63452	GM12878	blood:	n/a	chr9:63315-63325
42	BATF	chr9:167629-168111	GM12878	blood:	n/a	n/a
43	BATF	chr9:185844-186146	GM12878	blood:	n/a	n/a
44	BATF	chr9:63198-63553	GM12878	blood:	n/a	chr9:63315-63325
45	BATF	chr9:88665-89067	GM12878	blood:	n/a	chr9:88843-88853 chr9:88842-88853
46	BATF	chr9:198812-199262	GM12878	blood:	n/a	chr9:198886-198895
47	BATF	chr9:164778-164998	GM12878	blood:	n/a	n/a
48	BATF	chr9:200387-200708	GM12878	blood:	n/a	chr9:200519-200530
49	BATF	chr9:120835-121041	GM12878	blood:	n/a	n/a
50	BATF	chr9:297420-297885	GM12878	blood:	n/a	chr9:297684-297695 chr9:297685-297695

(count:1833 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:273072-273122	A549	lung:	n/a
2	chr9:118091-118141	SK-N-SH	brain:	n/a
3	chr9:73704-73754	HNPCEpiC	eye:	n/a
4	chr9:273072-273122	A549	lung:	n/a
5	chr9:118091-118141	SK-N-SH	brain:	n/a
6	chr9:73704-73754	HNPCEpiC	eye:	n/a
7	chr9:114359-114409	HRPEpiC	eye:	n/a
8	chr9:73835-73885	NB4	blood:	n/a
9	chr9:114838-114888	HIPEpiC	eye:	n/a
10	chr9:73704-73754	IMR90	lung:	fetal
11	chr9:104568-104618	HCPEpiC	choroid plexus:	n/a
12	chr9:114434-114484	HCPEpiC	choroid plexus:	n/a
13	chr9:114838-114888	NHBE	bronchial:	n/a
14	chr9:113530-113580	HAEpiC	amniotic membrane:	n/a
15	chr9:114434-114484	HNPCEpiC	eye:	n/a
16	chr9:117608-117658	GM12878	blood:	n/a
17	chr9:72908-72958	GM19239	blood:	n/a
18	chr9:179409-179459	HCPEpiC	choroid plexus:	n/a
19	chr9:117608-117658	SK-N-SH_RA	brain:	n/a
20	chr9:118698-118748	NHDF-neo	bronchial:	n/a
21	chr9:114140-114190	HCF	heart:	n/a
22	chr9:118530-118580	LNCaP	prostate:	n/a
23	chr9:215368-215418	HMEC	breast:	n/a
24	chr9:215561-215611	AG04450	lung:	fetal
25	chr9:176893-176943	Jurkat	blood:	n/a
26	chr9:114359-114409	CMK	blood:	n/a
27	chr9:213650-213700	BJ	skin:	n/a
28	chr9:214690-214740	HEEpiC	esophagus:	n/a
29	chr9:113530-113580	HEK293	kidney:	embryo
30	chr9:112618-112668	GM19239	blood:	n/a
31	chr9:73835-73885	HCT-116	colon:	n/a
32	chr9:118698-118748	K562	blood:	n/a
33	chr9:168828-168878	H1-hESC	embryonic stem cell:	embryo
34	chr9:114140-114190	Caco-2	colon:	n/a
35	chr9:168828-168878	LNCaP	prostate:	n/a
36	chr9:72908-72958	SK-N-MC	brain:	n/a
37	chr9:214268-214318	AG04449	skin:	fetal
38	chr9:215368-215418	A549	lung:	n/a
39	chr9:117608-117658	Jurkat	blood:	n/a
40	chr9:112937-112987	SK-N-SH	brain:	n/a
41	chr9:118091-118141	HRCEpiC	kidney:	n/a
42	chr9:214690-214740	HEK293	kidney:	embryo
43	chr9:114140-114190	SK-N-SH	brain:	n/a
44	chr9:113530-113580	NB4	blood:	n/a
45	chr9:114359-114409	HPAEpiC	pulmonary alveolar:	n/a
46	chr9:117608-117658	HCF	heart:	n/a
47	chr9:72961-73011	CMK	blood:	n/a
48	chr9:117044-117094	NB4	blood:	n/a
49	chr9:112618-112668	MCF-7	breast:	n/a
50	chr9:112618-112668	T-47D	breast:	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr9:243324..246093-chr9:246428..250809,6	K562	blood:
2	chr9:283346..286966-chr9:287946..290894,7	K562	blood:
3	chr9:265556..268525-chr9:268878..270498,2	K562	blood:
4	chr9:226722..229215-chr9:247840..250679,2	K562	blood:
5	chr9:246962..249799-chr9:250077..252857,2	K562	blood:
6	chr9:262046..270232-chr9:270847..276392,11	K562	blood:
7	chr9:247322..249745-chr9:277912..279940,2	K562	blood:
8	chr9:224695..226653-chr9:227779..229816,2	K562	blood:
9	chr9:224171..226015-chr9:253370..255238,2	MCF-7	breast:
10	chr9:284961..287002-chr9:306876..309185,2	K562	blood:
11	chr9:213868..216890-chr9:248711..251891,4	K562	blood:
12	chr9:316274..318543-chr9:331270..334145,2	MCF-7	breast:
13	chr9:223210..226112-chr9:277917..282090,3	K562	blood:
14	chr9:252242..255061-chr9:271559..273805,3	K562	blood:
15	chr9:211912..213756-chr9:227781..229604,2	K562	blood:
16	chr9:268983..271562-chr9:284279..286719,2	MCF-7	breast:
17	chr9:213589..216422-chr9:270983..274599,7	K562	blood:
18	chr9:318530..320927-chr9:322721..325349,2	K562	blood:
19	chr9:275975..278627-chr9:279451..282123,3	K562	blood:
20	chr9:224695..226653-chr9:227779..229816,2	K562	blood:
21	chr9:213518..215162-chr9:305580..308186,2	K562	blood:
22	chr9:237820..240828-chr9:247584..251042,3	K562	blood:
23	chr9:213410..215081-chr9:270583..272682,2	MCF-7	breast:
24	chr9:264854..268401-chr9:271602..276392,5	K562	blood:
25	chr9:303334..306488-chr9:313112..315414,3	MCF-7	breast:
26	chr9:214091..217459-chr9:295851..299102,3	MCF-7	breast:
27	chr9:216842..219174-chr9:220888..224256,4	K562	blood:
28	chr9:276314..278461-chr9:285139..287718,2	K562	blood:
29	chr9:207956..209819-chr9:211466..213662,2	MCF-7	breast:
30	chr9:288365..290115-chr9:299185..301598,2	MCF-7	breast:
31	chr9:207715..211592-chr9:270281..275557,5	K562	blood:
32	chr9:213452..215018-chr9:305580..307976,2	K562	blood:
33	chr9:214856..218562-chr9:240584..242539,3	K562	blood:
34	chr9:214996..215595-chr9:307020..307600,2	MCF-7	breast:
35	chr9:210795..213326-chr9:213922..216378,4	MCF-7	breast:
36	chr9:244363..245872-chr9:248878..250809,2	K562	blood:
37	chr9:244363..245872-chr9:248878..250809,2	K562	blood:
38	chr9:211790..213319-chr9:241598..244495,2	K562	blood:
39	chr9:284961..287002-chr9:306876..309185,2	K562	blood:
40	chr9:211912..213756-chr9:227781..229604,2	K562	blood:
41	chr9:277861..283096-chr9:291676..296273,5	K562	blood:
42	chr9:223210..226112-chr9:277917..282090,3	K562	blood:
43	chr9:288330..291260-chr9:302503..304653,3	K562	blood:
44	chr9:250806..252981-chr9:269858..272236,2	MCF-7	breast:
45	chr9:216842..219174-chr9:220888..224256,4	K562	blood:
46	chr9:303334..306488-chr9:313112..315414,3	MCF-7	breast:
47	chr9:285389..289218-chr9:290727..294143,4	K562	blood:
48	chr9:240408..242135-chr9:247395..249007,2	MCF-7	breast:
49	chr9:265556..268525-chr9:268878..270498,2	K562	blood:
50	chr9:237104..239333-chr9:240417..242425,2	K562	blood:

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

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

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
ENSG00000235880	chromatin interactions
ENSG00000107099	chromatin interactions
ENSG00000101191	chromatin interactions
ENSG00000183784	chromatin interactions

Extended variants
information (count: 10062 )
Associated
traits (count: 123 )

Variant overlapped rSNPs/rCNVs (count:10062 , 50 per page) page: 1 2 3 4 5 6 7 ... 202

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs576583467	chr9:62899-62900	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs148138591	chr9:62922-62923	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs565397315	chr9:62962-62963	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs577241369	chr9:62964-62965	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs541105786	chr9:63013-63014	Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs556745631	chr9:63078-63079	Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs559355952	chr9:63093-63094	Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs200730339	chr9:63110-63111	Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs181076308	chr9:63112-63113	Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs548126299	chr9:63169-63170	Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs185285307	chr9:63175-63176	Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs530741768	chr9:63180-63181	Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs147301077	chr9:63197-63198	Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs191062357	chr9:63205-63206	Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs534733329	chr9:63223-63224	Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs144948975	chr9:63224-63225	Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs568101124	chr9:63320-63321	Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs535438183	chr9:63331-63332	Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs9407301	chr9:63398-63399	Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs555254706	chr9:63410-63411	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs371077639	chr9:63424-63425	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs576628203	chr9:63433-63434	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs537675862	chr9:63468-63469	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs558913516	chr9:63470-63471	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs577008721	chr9:63479-63480	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs150004105	chr9:63486-63487	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs559418885	chr9:63524-63525	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs145289965	chr9:63529-63530	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs183859433	chr9:63571-63572	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs563614584	chr9:63609-63610	Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs11999617	chr9:63634-63635	Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs2811045	chr9:63635-63636	Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs199798080	chr9:63640-63641	Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs553210446	chr9:63653-63654	Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs546053182	chr9:63671-63672	Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs564157397	chr9:63675-63676	Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs9299014	chr9:63801-63802	Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs528284330	chr9:63849-63850	Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs546762358	chr9:63869-63870	Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs568123549	chr9:63873-63874	Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs2998923	chr9:63924-63925	Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs528914514	chr9:63995-63996	Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs550281911	chr9:64025-64026	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs201990727	chr9:64026-64027	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs372704546	chr9:64109-64110	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs199571471	chr9:64118-64119	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs539038403	chr9:64179-64180	Enhancers Flanking Active TSS Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
48	rs568816175	chr9:64189-64190	Enhancers Flanking Active TSS Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
49	rs537378409	chr9:64204-64205	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
50	rs142595565	chr9:64209-64210	Weak transcription 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:2878 , 50 per page) page: 1 2 3 4 5 6 7 ... 58

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

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