Variant report

Variant	nsv1033689
Chromosome Location	chr9:88018-358384
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3020)
CpG islands
(count:1527)
Chromatin interactive
region (count:135)
LncRNA
region (count:29)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:3020 , 50 per page) page: 1 2 3 4 5 6 7 ... 61

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:210220-210873	K562	blood:	n/a	n/a
2	ARID3A	chr9:215966-216247	K562	blood:	n/a	n/a
3	ARID3A	chr9:94438-94633	K562	blood:	n/a	chr9:94582-94598
4	ARID3A	chr9:250210-251866	K562	blood:	n/a	n/a
5	ARID3A	chr9:229136-229466	K562	blood:	n/a	n/a
6	ARID3A	chr9:336046-336405	HepG2	liver:	n/a	n/a
7	ARID3A	chr9:237608-238477	K562	blood:	n/a	n/a
8	ARID3A	chr9:214214-215154	K562	blood:	n/a	n/a
9	ARID3A	chr9:267916-268404	K562	blood:	n/a	n/a
10	ARID3A	chr9:95057-95158	K562	blood:	n/a	n/a
11	ARID3A	chr9:272095-272522	K562	blood:	n/a	n/a
12	ARID3A	chr9:260270-260544	K562	blood:	n/a	n/a
13	ARID3A	chr9:238911-239096	K562	blood:	n/a	n/a
14	ARID3A	chr9:272758-273406	K562	blood:	n/a	chr9:273064-273079
15	ATF1	chr9:272150-272512	K562	blood:	n/a	n/a
16	ATF1	chr9:249153-249485	K562	blood:	n/a	n/a
17	ATF1	chr9:211078-211816	K562	blood:	n/a	n/a
18	ATF1	chr9:222266-222777	K562	blood:	n/a	n/a
19	ATF1	chr9:270753-271026	K562	blood:	n/a	n/a
20	ATF1	chr9:94435-94576	K562	blood:	n/a	n/a
21	ATF1	chr9:272781-273161	K562	blood:	n/a	n/a
22	ATF1	chr9:312958-313372	K562	blood:	n/a	n/a
23	ATF2	chr9:297286-297859	GM12878	blood:	n/a	n/a
24	ATF2	chr9:272677-273240	GM12878	blood:	n/a	n/a
25	ATF2	chr9:272650-273286	GM12878	blood:	n/a	n/a
26	ATF3	chr9:326568-327022	H1-hESC	embryonic stem cell:	n/a	n/a
27	ATF3	chr9:210212-210461	K562	blood:	n/a	n/a
28	ATF3	chr9:272081-272576	K562	blood:	n/a	n/a
29	BACH1	chr9:114203-114262	H1-hESC	embryonic stem cell:	n/a	n/a
30	BACH1	chr9:214677-214706	H1-hESC	embryonic stem cell:	n/a	n/a
31	BACH1	chr9:113631-113796	H1-hESC	embryonic stem cell:	n/a	n/a
32	BACH1	chr9:207498-207603	K562	blood:	n/a	n/a
33	BACH1	chr9:214910-215270	H1-hESC	embryonic stem cell:	n/a	n/a
34	BATF	chr9:152906-153110	GM12878	blood:	n/a	chr9:152982-152993
35	BATF	chr9:198812-199262	GM12878	blood:	n/a	chr9:198886-198895
36	BATF	chr9:183522-184128	GM12878	blood:	n/a	n/a
37	BATF	chr9:199639-200066	GM12878	blood:	n/a	n/a
38	BATF	chr9:156921-157465	GM12878	blood:	n/a	n/a
39	BATF	chr9:278668-278987	GM12878	blood:	n/a	n/a
40	BATF	chr9:185826-186168	GM12878	blood:	n/a	n/a
41	BATF	chr9:88665-89067	GM12878	blood:	n/a	chr9:88843-88853 chr9:88842-88853
42	BATF	chr9:156926-157447	GM12878	blood:	n/a	n/a
43	BATF	chr9:156635-156839	GM12878	blood:	n/a	n/a
44	BATF	chr9:164778-164998	GM12878	blood:	n/a	n/a
45	BATF	chr9:122820-123095	GM12878	blood:	n/a	n/a
46	BATF	chr9:297420-297885	GM12878	blood:	n/a	chr9:297684-297695 chr9:297685-297695
47	BATF	chr9:167541-168102	GM12878	blood:	n/a	n/a
48	BATF	chr9:177184-177383	GM12878	blood:	n/a	n/a
49	BATF	chr9:178394-179363	GM12878	blood:	n/a	chr9:179069-179082
50	BATF	chr9:199669-200113	GM12878	blood:	n/a	n/a

(count:1527 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:215561-215611	PANC-1	pancreas:	n/a
2	chr9:273072-273122	HL-60	blood:	n/a
3	chr9:215561-215611	PANC-1	pancreas:	n/a
4	chr9:273072-273122	HL-60	blood:	n/a
5	chr9:214612-214662	Hepatocyte	liver:	n/a
6	chr9:109039-109089	GM12891	blood:	n/a
7	chr9:112937-112987	A549	lung:	n/a
8	chr9:179409-179459	HUVEC	blood vessel:	n/a
9	chr9:211689-211739	Caco-2	colon:	n/a
10	chr9:118530-118580	MCF-7	breast:	n/a
11	chr9:113530-113580	HEEpiC	esophagus:	n/a
12	chr9:117608-117658	U87	brain:	n/a
13	chr9:176893-176943	CMK	blood:	n/a
14	chr9:211689-211739	Hela-S3	cervix:	n/a
15	chr9:118530-118580	HL-60	blood:	n/a
16	chr9:114434-114484	K562	blood:	n/a
17	chr9:273072-273122	HCT-116	colon:	n/a
18	chr9:112937-112987	Hepatocyte	liver:	n/a
19	chr9:118698-118748	HL-60	blood:	n/a
20	chr9:214268-214318	NHBE	bronchial:	n/a
21	chr9:118091-118141	HCM	heart:	n/a
22	chr9:112937-112987	AG04450	lung:	fetal
23	chr9:215368-215418	H1-hESC	embryonic stem cell:	embryo
24	chr9:176893-176943	GM12892	blood:	n/a
25	chr9:112937-112987	ECC-1	luminal epithelium:	n/a
26	chr9:213650-213700	GM19239	blood:	n/a
27	chr9:114434-114484	AG10803	skin:	n/a
28	chr9:168828-168878	U87	brain:	n/a
29	chr9:211689-211739	HRPEpiC	eye:	n/a
30	chr9:114140-114190	SAEC	small airway:	n/a
31	chr9:114434-114484	NB4	blood:	n/a
32	chr9:117608-117658	NH-A	brain:	n/a
33	chr9:114140-114190	AoSMC	blood vessel:	n/a
34	chr9:215368-215418	BE2_C	brain:	n/a
35	chr9:104568-104618	HRE	kidney:	n/a
36	chr9:117044-117094	A549	lung:	n/a
37	chr9:109039-109089	MCF-7	breast:	n/a
38	chr9:114838-114888	HAEpiC	amniotic membrane:	n/a
39	chr9:214268-214318	AG04450	lung:	fetal
40	chr9:114838-114888	NHBE	bronchial:	n/a
41	chr9:118698-118748	H1-hESC	embryonic stem cell:	embryo
42	chr9:117608-117658	HEEpiC	esophagus:	n/a
43	chr9:214268-214318	ovcar-3	ovarian:	n/a
44	chr9:176893-176943	NHDF-neo	bronchial:	n/a
45	chr9:114140-114190	HRPEpiC	eye:	n/a
46	chr9:112937-112987	NB4	blood:	n/a
47	chr9:117608-117658	SK-N-SH_RA	brain:	n/a
48	chr9:113530-113580	AG09309	skin:	n/a
49	chr9:215368-215418	HAEpiC	amniotic membrane:	n/a
50	chr9:179409-179459	SK-N-MC	brain:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr9:265556..268525-chr9:268878..270498,2	K562	blood:
2	chr9:213410..215081-chr9:270583..272682,2	MCF-7	breast:
3	chr9:286841..289218-chr9:291668..294143,2	K562	blood:
4	chr9:213656..215329-chr9:262330..263868,2	K562	blood:
5	chr9:316274..318543-chr9:331270..334145,2	MCF-7	breast:
6	chr9:246962..249799-chr9:250077..252857,2	K562	blood:
7	chr9:235818..237375-chr9:247234..248835,2	K562	blood:
8	chr9:240408..242135-chr9:247395..249007,2	MCF-7	breast:
9	chr9:224171..226015-chr9:253370..255238,2	MCF-7	breast:
10	chr9:207871..210695-chr9:212521..216858,5	MCF-7	breast:
11	chr9:211395..217021-chr9:276782..283147,8	K562	blood:
12	chr9:318530..320927-chr9:322721..325349,2	K562	blood:
13	chr9:255761..258409-chr9:263285..266102,2	K562	blood:
14	chr9:211063..213249-chr9:216572..219831,3	K562	blood:
15	chr9:255761..258409-chr9:263285..266102,2	K562	blood:
16	chr9:214778..216543-chr9:219574..221163,2	MCF-7	breast:
17	chr9:271874..274602-chr9:275665..279412,3	K562	blood:
18	chr9:257830..262248-chr9:271354..273884,5	K562	blood:
19	chr9:239328..240900-chr9:247584..249872,2	K562	blood:
20	chr9:261493..264345-chr9:269680..272564,2	MCF-7	breast:
21	chr9:211790..213319-chr9:241598..244495,2	K562	blood:
22	chr20:61557637..61559255-chr9:214332..216174,2	MCF-7	breast:
23	chr9:276314..278461-chr9:285139..287718,2	K562	blood:
24	chr9:217275..219531-chr9:301975..303827,2	MCF-7	breast:
25	chr9:237104..239333-chr9:240417..242425,2	K562	blood:
26	chr9:223853..225771-chr9:261619..263535,2	K562	blood:
27	chr9:213868..216890-chr9:248711..251891,4	K562	blood:
28	chr9:350965..353575-chr9:397923..399924,2	K562	blood:
29	chr9:214856..218562-chr9:240584..242539,3	K562	blood:
30	chr9:213603..216956-chr9:218226..220394,3	K562	blood:
31	chr9:214285..216173-chr9:227690..229444,2	K562	blood:
32	chr9:211912..213756-chr9:227781..229604,2	K562	blood:
33	chr9:211063..213249-chr9:216572..219831,3	K562	blood:
34	chr9:213452..215018-chr9:305580..307976,2	K562	blood:
35	chr9:218197..221460-chr9:224650..228237,4	K562	blood:
36	chr9:216842..219174-chr9:220888..224256,4	K562	blood:
37	chr9:212545..218648-chr9:270340..281940,20	K562	blood:
38	chr9:284961..287002-chr9:306876..309185,2	K562	blood:
39	chr9:324085..328451-chr9:329787..332698,3	K562	blood:
40	chr9:268889..271022-chr9:277493..279614,2	K562	blood:
41	chr9:284961..287002-chr9:306876..309185,2	K562	blood:
42	chr9:210056..211721-chr9:271493..274380,2	K562	blood:
43	chr9:268983..271562-chr9:284279..286719,2	MCF-7	breast:
44	chr9:235818..237375-chr9:247234..248835,2	K562	blood:
45	chr9:347287..349476-chr9:362112..363970,2	MCF-7	breast:
46	chr9:210795..213326-chr9:213922..216378,4	MCF-7	breast:
47	chr9:347797..348410-chr9:459774..460369,2	MCF-7	breast:
48	chr9:240408..242135-chr9:247395..249007,2	MCF-7	breast:
49	chr9:211912..213756-chr9:227781..229604,2	K562	blood:
50	chr9:239328..240900-chr9:247584..249872,2	K562	blood:

(count:29 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FOXD4-2	chr9:109596-109842	NONHSAT129897
2	lnc-DOCK8-3	chr9:88742-88826	ENSG00000225655.1
3	lnc-FOXD4-1	chr9:112716-113067	ENSG00000231808
4	lnc-FOXD4-2	chr9:101002-101304	ENSG00000227917
5	lnc-FOXD4-4	chr9:91002-91304	NONHSAT129893
6	lnc-FOXD4-3	chr9:114040-115772	NONHSAT129899
7	lnc-FOXD4-4	chr9:92473-92541	NONHSAT129893
8	lnc-C9orf66-1	chr9:267966-268273	ENSG00000235880.1
9	lnc-FOXD4-4	chr9:92740-92850	NONHSAT129892
10	lnc-FOXD4-5	chr9:151745-152078	NONHSAT129910
11	lnc-FOXD4-5	chr9:161567-161647	NONHSAT129910
12	lnc-FOXD4-4	chr9:90804-91304	NONHSAT129892
13	lnc-FOXD4-2	chr9:102473-102541	ENSG00000227917
14	lnc-FOXD4-2	chr9:108804-109469	NONHSAT129897
15	lnc-FOXD4-4	chr9:90995-91304	ucscGeneNc_uc003zfy_2
16	lnc-FOXD4-2	chr9:109316-109471	NONHSAT129895
17	lnc-C9orf66-1	chr9:272905-273002	ENSG00000235880.1
18	lnc-FOXD4-1	chr9:113694-113754	ENSG00000231808
19	lnc-FOXD4-2	chr9:102716-103067	NONHSAT129896
20	lnc-FOXD4-2	chr9:103694-103754	NONHSAT129896
21	lnc-FOXD4-5	chr9:154709-154795	NONHSAT129910
22	lnc-FOXD4-2	chr9:101014-101304	NONHSAT129895
23	lnc-FOXD4-4	chr9:92740-92941	ucscGeneNc_uc003zfy_2
24	lnc-FOXD4-3	chr9:113606-113656	NONHSAT129899
25	lnc-FOXD4-2	chr9:102740-102941	ENSG00000227917
26	lnc-FOXD4-4	chr9:92740-92941	NONHSAT129893
27	lnc-FOXD4-4	chr9:92473-92541	ucscGeneNc_uc003zfy_2
28	lnc-FOXD4-2	chr9:102740-102850	NONHSAT129895
29	lnc-FOXD4-5	chr9:156481-156527	NONHSAT129910

No data

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

Extended variants
information (count: 11745 )
Associated
traits (count: 123 )

Variant overlapped rSNPs/rCNVs (count:11745 , 50 per page) page: 1 2 3 4 5 6 7 ... 235

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs56706531	chr9:88022-88023	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs184825310	chr9:88054-88055	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs571228833	chr9:88091-88092	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs56091827	chr9:88120-88121	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs59314848	chr9:88122-88123	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs2811102	chr9:88130-88131	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs374474726	chr9:88161-88162	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs553522858	chr9:88187-88188	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs141470825	chr9:88205-88206	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs2811103	chr9:88210-88211	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs374940288	chr9:88211-88212	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs534271289	chr9:88215-88216	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs556055379	chr9:88219-88220	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs59820801	chr9:88229-88230	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs569906079	chr9:88233-88234	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs370905533	chr9:88237-88238	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs138845971	chr9:88238-88239	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs374537962	chr9:88241-88242	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs368829200	chr9:88245-88246	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs2811104	chr9:88254-88255	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs544786928	chr9:88267-88268	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs2811105	chr9:88268-88269	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs56110998	chr9:88281-88282	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs556771293	chr9:88294-88295	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs578060706	chr9:88317-88318	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs545471681	chr9:88322-88323	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs57162446	chr9:88339-88340	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs60951482	chr9:88346-88347	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs560328002	chr9:88349-88350	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs527639867	chr9:88356-88357	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs371734860	chr9:88385-88386	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs61300527	chr9:88388-88389	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs542524667	chr9:88394-88395	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs556600177	chr9:88398-88399	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs4595196	chr9:88406-88407	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs147443240	chr9:88459-88460	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs549593967	chr9:88461-88462	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs200343361	chr9:88464-88465	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs56662846	chr9:88465-88466	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs186723303	chr9:88466-88467	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs61120779	chr9:88474-88475	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs2259901	chr9:88501-88502	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs200374949	chr9:88503-88504	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs143872891	chr9:88516-88517	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs532149593	chr9:88531-88532	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs2259896	chr9:88544-88545	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs547466846	chr9:88604-88605	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs565548816	chr9:88654-88655	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs113539739	chr9:88672-88673	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs553702625	chr9:88674-88675	Weak transcription	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:3042 , 50 per page) page: 1 2 3 4 5 6 7 ... 61

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:87800-88600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
2	chr9:88400-88600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr9:88600-94000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr9:94000-94200	Enhancers	K562	blood
5	chr9:94000-95600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr9:94200-95200	Weak transcription	K562	blood
7	chr9:95000-95800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr9:95200-95600	Enhancers	K562	blood
9	chr9:98000-98400	Enhancers	Primary T cells fromperipheralblood	blood
10	chr9:98000-98600	Enhancers	Primary B cells from peripheral blood	blood
11	chr9:98000-98600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
12	chr9:98000-98800	Enhancers	Primary T regulatory cells fromperipheralblood	blood
13	chr9:102600-102800	ZNF genes & repeats	Lung	lung
14	chr9:108800-109000	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
15	chr9:108800-109000	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
16	chr9:108800-109000	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
17	chr9:108800-109000	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
18	chr9:109200-109400	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
19	chr9:109200-109400	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
20	chr9:109200-109400	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr9:109200-110000	Bivalent Enhancer	Skeletal Muscle Female	skeletal muscle
22	chr9:112800-113000	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
23	chr9:112800-113000	Bivalent Enhancer	Primary T helper memory cells from peripheral blood 2	blood
24	chr9:112800-113000	Bivalent Enhancer	Primary T helper naive cells from peripheral blood	blood
25	chr9:112800-113000	Bivalent Enhancer	Brain Hippocampus Middle	brain
26	chr9:112800-113000	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
27	chr9:112800-113000	Bivalent Enhancer	K562	blood
28	chr9:112800-113200	Bivalent Enhancer	Fetal Muscle Leg	muscle
29	chr9:112800-113400	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
30	chr9:112800-113400	Bivalent Enhancer	Primary T helper 17 cells PMA-I stimulated	--
31	chr9:112800-113400	Bivalent Enhancer	Primary T helper cells fromperipheralblood	blood
32	chr9:112800-113400	Bivalent Enhancer	Primary T regulatory cells fromperipheralblood	blood
33	chr9:112800-113400	Bivalent Enhancer	Primary T cells effector/memory enriched fromperipheralblood	blood
34	chr9:112800-113400	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
35	chr9:112800-113400	Bivalent Enhancer	Adipose Nuclei	Adipose
36	chr9:112800-113400	Bivalent Enhancer	Duodenum Smooth Muscle	Duodenum
37	chr9:112800-113400	Bivalent/Poised TSS	Right Ventricle	heart
38	chr9:112800-113400	Bivalent Enhancer	Monocytes-CD14+_RO01746	blood
39	chr9:112800-113600	Bivalent Enhancer	Primary T helper cells PMA-I stimulated	--
40	chr9:112800-113600	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
41	chr9:112800-113800	Bivalent Enhancer	Primary B cells from peripheral blood	blood
42	chr9:112800-113800	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
43	chr9:112800-114000	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
44	chr9:112800-115200	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
45	chr9:112800-115400	Flanking Bivalent TSS/Enh	Fetal Muscle Trunk	muscle
46	chr9:113000-113200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr9:113000-113200	Active TSS	Primary hematopoietic stem cells short term culture	blood
48	chr9:113000-113200	Bivalent Enhancer	Fetal Intestine Large	intestine
49	chr9:113000-113400	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
50	chr9:113000-113400	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain

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