Variant report

Variant	nsv831500
Chromosome Location	chr9:6847952-6992535
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1530)
CpG islands
(count:244)
Chromatin interactive
region (count:35)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1530 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:6896535-6896910	K562	blood:	n/a	n/a
2	ARID3A	chr9:6910048-6910291	K562	blood:	n/a	n/a
3	ARID3A	chr9:6900480-6901015	HepG2	liver:	n/a	n/a
4	ARID3A	chr9:6986412-6986867	HepG2	liver:	n/a	n/a
5	ARID3A	chr9:6955127-6955771	HepG2	liver:	n/a	n/a
6	ARID3A	chr9:6871154-6871863	HepG2	liver:	n/a	n/a
7	ARID3A	chr9:6931921-6932276	K562	blood:	n/a	n/a
8	ARID3A	chr9:6899014-6899731	HepG2	liver:	n/a	n/a
9	ARID3A	chr9:6932065-6932168	HepG2	liver:	n/a	n/a
10	ARID3A	chr9:6927709-6928185	K562	blood:	n/a	n/a
11	ARID3A	chr9:6896614-6898522	HepG2	liver:	n/a	chr9:6897723-6897739 chr9:6897724-6897740
12	ARID3A	chr9:6877521-6878180	HepG2	liver:	n/a	n/a
13	ATF1	chr9:6931877-6932320	K562	blood:	n/a	n/a
14	ATF1	chr9:6927695-6928152	K562	blood:	n/a	n/a
15	ATF1	chr9:6896588-6896942	K562	blood:	n/a	n/a
16	ATF1	chr9:6894414-6894608	K562	blood:	n/a	n/a
17	ATF2	chr9:6893660-6894746	GM12878	blood:	n/a	n/a
18	ATF2	chr9:6973498-6974318	GM12878	blood:	n/a	n/a
19	ATF2	chr9:6902404-6902842	GM12878	blood:	n/a	n/a
20	ATF2	chr9:6893949-6894575	GM12878	blood:	n/a	n/a
21	ATF2	chr9:6973706-6974207	GM12878	blood:	n/a	n/a
22	ATF2	chr9:6960665-6961260	GM12878	blood:	n/a	n/a
23	ATF2	chr9:6917103-6917695	GM12878	blood:	n/a	n/a
24	ATF3	chr9:6931886-6932304	K562	blood:	n/a	n/a
25	ATF3	chr9:6896530-6896937	K562	blood:	n/a	n/a
26	BACH1	chr9:6955248-6955617	H1-hESC	embryonic stem cell:	n/a	chr9:6955424-6955438
27	BACH1	chr9:6854906-6854915	H1-hESC	embryonic stem cell:	n/a	n/a
28	BATF	chr9:6973808-6974185	GM12878	blood:	n/a	chr9:6973978-6973989
29	BATF	chr9:6894106-6894608	GM12878	blood:	n/a	n/a
30	BATF	chr9:6923191-6923398	GM12878	blood:	n/a	n/a
31	BATF	chr9:6894207-6894592	GM12878	blood:	n/a	n/a
32	BATF	chr9:6973758-6974189	GM12878	blood:	n/a	chr9:6973978-6973989
33	BCL11A	chr9:6973797-6974200	GM12878	blood:	n/a	n/a
34	BCL11A	chr9:6917243-6917586	GM12878	blood:	n/a	n/a
35	BCL11A	chr9:6973811-6974164	GM12878	blood:	n/a	n/a
36	BCL11A	chr9:6894214-6894574	GM12878	blood:	n/a	n/a
37	BCL11A	chr9:6893817-6893964	GM12878	blood:	n/a	n/a
38	BCLAF1	chr9:6894120-6894571	GM12878	blood:	n/a	n/a
39	BCLAF1	chr9:6973634-6974239	GM12878	blood:	n/a	n/a
40	BHLHE40	chr9:6896595-6896959	K562	blood:	n/a	n/a
41	BHLHE40	chr9:6955450-6955720	GM12878	blood:	n/a	n/a
42	BHLHE40	chr9:6897814-6898300	HepG2	liver:	n/a	n/a
43	BHLHE40	chr9:6894236-6894572	GM12878	blood:	n/a	n/a
44	BHLHE40	chr9:6925145-6925210	K562	blood:	n/a	n/a
45	BHLHE40	chr9:6931869-6932449	K562	blood:	n/a	n/a
46	BHLHE40	chr9:6955289-6955945	HepG2	liver:	n/a	n/a
47	BRCA1	chr9:6945537-6945561	Hela-S3	cervix:	n/a	n/a
48	CBX3	chr9:6927751-6928155	K562	blood:	n/a	n/a
49	CBX3	chr9:6896517-6896894	K562	blood:	n/a	n/a
50	CBX3	chr9:6931729-6932402	HCT-116	colon:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:6932042-6932092	HRPEpiC	eye:	n/a
2	chr9:6932042-6932092	HCT-116	colon:	n/a
3	chr9:6921930-6921980	H1-hESC	embryonic stem cell:	embryo
4	chr9:6932042-6932092	NH-A	brain:	n/a
5	chr9:6921930-6921980	Jurkat	blood:	n/a
6	chr9:6955559-6955609	HEEpiC	esophagus:	n/a
7	chr9:6869699-6869749	PrEC	prostate:	n/a
8	chr9:6869699-6869749	HPAEpiC	pulmonary alveolar:	n/a
9	chr9:6932042-6932092	HAEpiC	amniotic membrane:	n/a
10	chr9:6955559-6955609	AG10803	skin:	n/a
11	chr9:6955559-6955609	Caco-2	colon:	n/a
12	chr9:6869699-6869749	HCPEpiC	choroid plexus:	n/a
13	chr9:6869699-6869749	SAEC	small airway:	n/a
14	chr9:6932042-6932092	GM19239	blood:	n/a
15	chr9:6921930-6921980	HRCEpiC	kidney:	n/a
16	chr9:6869699-6869749	HRE	kidney:	n/a
17	chr9:6932042-6932092	H1-hESC	embryonic stem cell:	embryo
18	chr9:6921930-6921980	NH-A	brain:	n/a
19	chr9:6921930-6921980	GM06990	blood:	n/a
20	chr9:6955559-6955609	ovcar-3	ovarian:	n/a
21	chr9:6955559-6955609	PANC-1	pancreas:	n/a
22	chr9:6955559-6955609	IMR90	lung:	fetal
23	chr9:6921930-6921980	HNPCEpiC	eye:	n/a
24	chr9:6921930-6921980	PFSK-1	brain:	n/a
25	chr9:6869699-6869749	HAEpiC	amniotic membrane:	n/a
26	chr9:6921930-6921980	NB4	blood:	n/a
27	chr9:6932042-6932092	Caco-2	colon:	n/a
28	chr9:6932042-6932092	SK-N-MC	brain:	n/a
29	chr9:6955559-6955609	NHDF-neo	bronchial:	n/a
30	chr9:6869699-6869749	HCF	heart:	n/a
31	chr9:6932042-6932092	T-47D	breast:	n/a
32	chr9:6869699-6869749	T-47D	breast:	n/a
33	chr9:6921930-6921980	U87	brain:	n/a
34	chr9:6921930-6921980	SK-N-SH_RA	brain:	n/a
35	chr9:6869699-6869749	ECC-1	luminal epithelium:	n/a
36	chr9:6869699-6869749	HCT-116	colon:	n/a
37	chr9:6869699-6869749	BE2_C	brain:	n/a
38	chr9:6932042-6932092	HRE	kidney:	n/a
39	chr9:6869699-6869749	HL-60	blood:	n/a
40	chr9:6932042-6932092	GM12892	blood:	n/a
41	chr9:6869699-6869749	AG04450	lung:	fetal
42	chr9:6955559-6955609	SKMC	muscle:	n/a
43	chr9:6955559-6955609	T-47D	breast:	n/a
44	chr9:6869699-6869749	A549	lung:	n/a
45	chr9:6869699-6869749	HRCEpiC	kidney:	n/a
46	chr9:6955559-6955609	HUVEC	blood vessel:	n/a
47	chr9:6955559-6955609	HRCEpiC	kidney:	n/a
48	chr9:6869699-6869749	AG09309	skin:	n/a
49	chr9:6932042-6932092	Hela-S3	cervix:	n/a
50	chr9:6955559-6955609	GM12878	blood:	n/a

(count:35 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:6842488..6845236-chr9:6852172..6854079,2	MCF-7	breast:
2	chr9:6972707..6974430-chr9:6976948..6979606,2	K562	blood:
3	chr9:6896046..6898374-chr9:6899883..6901481,2	K562	blood:
4	chr9:6972707..6974430-chr9:6976948..6979606,2	K562	blood:
5	chr9:6952608..6955450-chr9:6959103..6961194,2	K562	blood:
6	chr9:6967812..6970366-chr9:6971584..6973778,2	K562	blood:
7	chr9:6978865..6981054-chr9:6982708..6984588,2	K562	blood:
8	chr9:6928105..6930890-chr9:6932209..6935061,3	K562	blood:
9	chr9:6921809..6924418-chr9:6928929..6932002,3	MCF-7	breast:
10	chr9:6845574..6847293-chr9:6858590..6860659,2	K562	blood:
11	chr9:6919963..6921657-chr9:6923857..6925524,2	K562	blood:
12	chr9:6986135..6988312-chr9:6992816..6995034,2	MCF-7	breast:
13	chr9:6931770..6934269-chr9:6942265..6944921,2	MCF-7	breast:
14	chr9:6892256..6893815-chr9:6903780..6905360,2	MCF-7	breast:
15	chr9:6967812..6970366-chr9:6971584..6973778,2	K562	blood:
16	chr9:6920289..6921801-chr9:7142294..7145025,2	K562	blood:
17	chr9:6896445..6898374-chr9:6899981..6902743,2	K562	blood:
18	chr9:6928105..6930890-chr9:6932209..6935061,3	K562	blood:
19	chr9:6890515..6892207-chr9:6893663..6895984,2	K562	blood:
20	chr9:6954682..6956612-chr9:6970287..6972358,2	MCF-7	breast:
21	chr9:6896046..6898374-chr9:6899883..6901481,2	K562	blood:
22	chr9:6890515..6892207-chr9:6893663..6895984,2	K562	blood:
23	chr9:6876130..6878078-chr9:6891371..6893102,2	K562	blood:
24	chr9:6921809..6924418-chr9:6928929..6932002,3	MCF-7	breast:
25	chr9:6931770..6934269-chr9:6942265..6944921,2	MCF-7	breast:
26	chr9:6954682..6956612-chr9:6970287..6972358,2	MCF-7	breast:
27	chr9:6881706..6883676-chr9:6890777..6893621,2	K562	blood:
28	chr9:6756573..6759030-chr9:6894279..6896008,2	K562	blood:
29	chr9:6888137..6890891-chr9:6891909..6894488,2	K562	blood:
30	chr9:6952608..6955450-chr9:6959103..6961194,2	K562	blood:
31	chr9:6909294..6911452-chr9:6925149..6926696,2	K562	blood:
32	chr9:6902386..6904166-chr9:6906939..6908570,2	K562	blood:
33	chr9:6876130..6878078-chr9:6891371..6893102,2	K562	blood:
34	chr9:6923976..6925853-chr9:6926210..6927942,2	K562	blood:
35	chr9:6755920..6758663-chr9:6904149..6906669,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-UHRF2-2	chr9:6974766-6974939	ENSG00000224972.1
2	lnc-UHRF2-2	chr9:6973827-6973887	ENSG00000224972.1
3	lnc-UHRF2-6	chr9:6941586-6941815	NONHSAT130166
4	lnc-UHRF2-6	chr9:6893123-6893232	NONHSAT130166
5	lnc-UHRF2-2	chr9:6902670-6902752	ENSG00000224972.1
6	lnc-UHRF2-6	chr9:6948033-6948214	NONHSAT130166
7	lnc-UHRF2-2	chr9:6978625-6978859	ENSG00000224972.1
8	lnc-UHRF2-6	chr9:6942460-6942634	NONHSAT130166

No data

Variant related genes	Relation type
ENSG00000224972	TF binding region
KDM4C	TF binding region
ENSG00000224972	CpG island
KDM4C	CpG island
ENSG00000107077	chromatin interactions
ENSG00000224972	chromatin interactions

Extended variants
information (count: 7589 )
Associated
traits (count: 107 )

Variant overlapped rSNPs/rCNVs (count:7589 , 50 per page) page: 1 2 3 4 5 6 7 ... 152

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs146714407	chr9:6847982-6847983	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs530945977	chr9:6848063-6848064	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs549085763	chr9:6848069-6848070	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs112082878	chr9:6848075-6848076	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs535350722	chr9:6848142-6848143	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs186222270	chr9:6848152-6848153	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs112102781	chr9:6848181-6848182	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs565688284	chr9:6848198-6848199	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs140344015	chr9:6848208-6848209	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs558027097	chr9:6848223-6848224	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs377008066	chr9:6848235-6848236	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs10975852	chr9:6848243-6848244	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs374040692	chr9:6848288-6848289	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs555036695	chr9:6848301-6848302	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs573597169	chr9:6848307-6848308	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs10815471	chr9:6848369-6848370	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs190249904	chr9:6848418-6848419	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs577957689	chr9:6848432-6848433	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs145533263	chr9:6848479-6848480	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs78120525	chr9:6848491-6848492	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs75588322	chr9:6848493-6848494	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs563568351	chr9:6848513-6848514	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs10975853	chr9:6848524-6848525	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs543120400	chr9:6848531-6848532	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs148925695	chr9:6848532-6848533	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs528487079	chr9:6848558-6848559	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs182130379	chr9:6848588-6848589	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs546726551	chr9:6848605-6848606	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs549013689	chr9:6848609-6848610	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs533303379	chr9:6848658-6848659	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs143669662	chr9:6848662-6848663	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs563282685	chr9:6848667-6848668	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs62535662	chr9:6848668-6848669	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs536713456	chr9:6848672-6848673	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs555450902	chr9:6848679-6848680	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs148112185	chr9:6848719-6848720	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs62535663	chr9:6848733-6848734	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs185262503	chr9:6848738-6848739	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs143934087	chr9:6848752-6848753	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs113618753	chr9:6848760-6848761	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs139195948	chr9:6848761-6848762	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs143234917	chr9:6848788-6848789	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs542706204	chr9:6848805-6848806	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs147527389	chr9:6848812-6848813	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs528620000	chr9:6848821-6848822	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs540607442	chr9:6848880-6848881	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs565310139	chr9:6848882-6848883	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs111989653	chr9:6848892-6848893	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs533238024	chr9:6848959-6848960	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs538526916	chr9:6848989-6848990	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:107)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	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
Disorders of sex development	21048976	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
Oral squamous cell carcinoma	17134496	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
Melanoma	18172304	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
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Developmental delay	21147756	CNVD
Lung cancer	18438408	CNVD
XY gonadal dysgenesis	20685758	CNVD
Urothelial carcinoma	21177765	CNVD
Oral cancer	21386901	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Myelodysplastic syndrome	21251322	CNVD
Breast cancer	21785460	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21858162	CNVD
Renal cell carcinoma	21668985	CNVD
Autism	22495311	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Myelofibrosis	22110671	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Hepatocellular carcinoma	18803288	CNVD
Breast cancer	21364760	CNVD
Metastatic melanoma	18483359	CNVD
Glioblastoma	19074898	CNVD
Malignant melanoma	19074898	CNVD
Prostate cancer	16573809	CNVD
Metanephric adenoma	20802469	CNVD
Medulloblastoma	16783165	CNVD
Medullary thyroid carcinoma	18765511	CNVD
Schizophrenia	23813976	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Ovarian clear cell carcinoma	21343371	CNVD

Chromatin state (count:3077 , 50 per page) page: 1 2 3 4 5 6 7 ... 62

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:6795000-6863800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
2	chr9:6795400-6849600	Weak transcription	HMEC	breast
3	chr9:6815400-6852000	Weak transcription	NHDF-Ad	bronchial
4	chr9:6816000-6856000	Weak transcription	Colon Smooth Muscle	Colon
5	chr9:6818800-6856000	Weak transcription	Psoas Muscle	Psoas
6	chr9:6819800-6853400	Weak transcription	Small Intestine	intestine
7	chr9:6824200-6849200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
8	chr9:6824200-6849600	Weak transcription	Primary neutrophils fromperipheralblood	blood
9	chr9:6824200-6860000	Weak transcription	Hela-S3	cervix
10	chr9:6824400-6892000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
11	chr9:6825400-6849800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr9:6831800-6849200	Weak transcription	Primary T helper cells PMA-I stimulated	--
13	chr9:6832000-6852800	Weak transcription	K562	blood
14	chr9:6834000-6854800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
15	chr9:6835200-6851200	Weak transcription	Placenta	Placenta
16	chr9:6835200-6851400	Weak transcription	HUES48 Cell Line	embryonic stem cell
17	chr9:6835200-6851800	Weak transcription	NHLF	lung
18	chr9:6835200-6854600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
19	chr9:6835200-6863800	Weak transcription	Brain Anterior Caudate	brain
20	chr9:6835400-6849400	Weak transcription	Duodenum Smooth Muscle	Duodenum
21	chr9:6835400-6849600	Weak transcription	Cortex derived primary cultured neurospheres	brain
22	chr9:6835400-6849600	Weak transcription	Stomach Smooth Muscle	stomach
23	chr9:6835400-6851600	Weak transcription	Fetal Brain Female	brain
24	chr9:6835400-6852200	Weak transcription	Fetal Muscle Trunk	muscle
25	chr9:6835400-6855000	Weak transcription	Rectal Smooth Muscle	rectum
26	chr9:6835400-6856400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
27	chr9:6835400-6863400	Weak transcription	H9 Cell Line	embryonic stem cell
28	chr9:6835400-6863400	Weak transcription	Ovary	ovary
29	chr9:6835400-6869200	Weak transcription	Right Ventricle	heart
30	chr9:6835400-6893200	Weak transcription	Colonic Mucosa	Colon
31	chr9:6835600-6849000	Weak transcription	Primary monocytes fromperipheralblood	blood
32	chr9:6835600-6849200	Weak transcription	Skeletal Muscle Female	skeletal muscle
33	chr9:6835600-6849400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
34	chr9:6835600-6849400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
35	chr9:6835600-6849400	Weak transcription	Dnd41	blood
36	chr9:6835600-6849600	Weak transcription	Adipose Nuclei	Adipose
37	chr9:6835600-6849600	Weak transcription	Rectal Mucosa Donor 29	rectum
38	chr9:6835600-6849600	Weak transcription	Rectal Mucosa Donor 31	rectum
39	chr9:6835600-6850400	Weak transcription	Fetal Stomach	stomach
40	chr9:6835600-6851000	Weak transcription	Thymus	Thymus
41	chr9:6835600-6851600	Weak transcription	HUES6 Cell Line	embryonic stem cell
42	chr9:6835600-6852000	Weak transcription	Skeletal Muscle Male	skeletal muscle
43	chr9:6835600-6852200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
44	chr9:6835600-6852200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
45	chr9:6835600-6852400	Weak transcription	Lung	lung
46	chr9:6835600-6852400	Weak transcription	Sigmoid Colon	Sigmoid Colon
47	chr9:6835600-6856600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
48	chr9:6835600-6863400	Weak transcription	Spleen	Spleen
49	chr9:6835600-6870600	Weak transcription	Esophagus	oesophagus
50	chr9:6835800-6849600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood

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