Variant report

Variant	nsv539927
Chromosome Location	chr9:2215179-2303623
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1255)
CpG islands
(count:550)
Chromatin interactive
region (count:34)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1255 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:2241752-2242185	HepG2	liver:	n/a	n/a
2	ARID3A	chr9:2241873-2242174	K562	blood:	n/a	n/a
3	ATF2	chr9:2241526-2242216	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr9:2281024-2281834	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr9:2229291-2229713	GM12878	blood:	n/a	n/a
6	ATF2	chr9:2241499-2242598	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr9:2281028-2281832	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF2	chr9:2229314-2229763	GM12878	blood:	n/a	n/a
9	ATF2	chr9:2241795-2242260	GM12878	blood:	n/a	n/a
10	ATF2	chr9:2241813-2242242	GM12878	blood:	n/a	n/a
11	ATF3	chr9:2241780-2242300	A549	lung:	n/a	n/a
12	BACH1	chr9:2241631-2242354	H1-hESC	embryonic stem cell:	n/a	n/a
13	BATF	chr9:2271359-2271697	GM12878	blood:	n/a	n/a
14	BATF	chr9:2271341-2271745	GM12878	blood:	n/a	n/a
15	BATF	chr9:2230017-2230285	GM12878	blood:	n/a	chr9:2230183-2230193 chr9:2230182-2230193
16	BCL11A	chr9:2241903-2242115	GM12878	blood:	n/a	n/a
17	BCL3	chr9:2241690-2242337	A549	lung:	n/a	n/a
18	BCL3	chr9:2241755-2242399	A549	lung:	n/a	n/a
19	BCLAF1	chr9:2229240-2229763	GM12878	blood:	n/a	chr9:2229561-2229570
20	BCLAF1	chr9:2241790-2242233	GM12878	blood:	n/a	n/a
21	BCLAF1	chr9:2241766-2242280	GM12878	blood:	n/a	n/a
22	BHLHE40	chr9:2241630-2242313	K562	blood:	n/a	n/a
23	BHLHE40	chr9:2241927-2242471	GM12878	blood:	n/a	n/a
24	BHLHE40	chr9:2241822-2242611	HepG2	liver:	n/a	n/a
25	BRCA1	chr9:2242326-2242348	GM12878	blood:	n/a	n/a
26	BRCA1	chr9:2241818-2242305	H1-hESC	embryonic stem cell:	n/a	n/a
27	CBX3	chr9:2241820-2242161	K562	blood:	n/a	n/a
28	CBX3	chr9:2260466-2261875	HCT-116	colon:	n/a	n/a
29	CBX3	chr9:2241713-2242381	HCT-116	colon:	n/a	n/a
30	CBX3	chr9:2260461-2261583	HCT-116	colon:	n/a	n/a
31	CBX3	chr9:2241725-2242505	HCT-116	colon:	n/a	n/a
32	CCNT2	chr9:2241616-2242096	K562	blood:	n/a	n/a
33	CEBPB	chr9:2227505-2227839	H1-hESC	embryonic stem cell:	n/a	chr9:2227644-2227655
34	CEBPB	chr9:2291981-2292807	MCF-7	breast:	n/a	n/a
35	CEBPB	chr9:2244293-2244527	A549	lung:	n/a	chr9:2244415-2244426
36	CEBPB	chr9:2291936-2292710	ECC-1	luminal epithelium:	n/a	n/a
37	CEBPB	chr9:2228159-2228502	A549	lung:	n/a	n/a
38	CEBPB	chr9:2244301-2244558	HepG2	liver:	n/a	chr9:2244415-2244426
39	CEBPB	chr9:2228058-2228601	A549	lung:	n/a	n/a
40	CEBPB	chr9:2241906-2242117	GM12878	blood:	n/a	n/a
41	CEBPB	chr9:2227482-2227798	A549	lung:	n/a	chr9:2227644-2227655
42	CEBPB	chr9:2228094-2228527	H1-hESC	embryonic stem cell:	n/a	n/a
43	CEBPB	chr9:2241419-2242557	H1-hESC	embryonic stem cell:	n/a	n/a
44	CEBPB	chr9:2297828-2298093	A549	lung:	n/a	chr9:2297948-2297959 chr9:2297947-2297960 chr9:2297949-2297958 chr9:2297947-2297960 chr9:2297947-2297958
45	CEBPB	chr9:2227489-2227810	K562	blood:	n/a	chr9:2227644-2227655
46	CEBPB	chr9:2270671-2270953	A549	lung:	n/a	chr9:2270774-2270785 chr9:2270773-2270784 chr9:2270773-2270784
47	CEBPB	chr9:2270673-2270933	IMR90	lung:	n/a	chr9:2270774-2270785 chr9:2270773-2270784 chr9:2270773-2270784
48	CEBPB	chr9:2228058-2228629	HCT-116	colon:	n/a	n/a
49	CEBPB	chr9:2297787-2298100	HepG2	liver:	n/a	chr9:2297948-2297959 chr9:2297947-2297960 chr9:2297949-2297958 chr9:2297947-2297960 chr9:2297947-2297958
50	CEBPB	chr9:2217015-2217182	HepG2	liver:	n/a	chr9:2217142-2217153

(count:550 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:2277780-2277830	Caco-2	colon:	n/a
2	chr9:2277780-2277830	Caco-2	colon:	n/a
3	chr9:2241256-2241306	HPAEpiC	pulmonary alveolar:	n/a
4	chr9:2234921-2234971	AG04450	lung:	fetal
5	chr9:2239671-2239721	HUVEC	blood vessel:	n/a
6	chr9:2239671-2239721	SK-N-SH_RA	brain:	n/a
7	chr9:2242468-2242518	HL-60	blood:	n/a
8	chr9:2241256-2241306	NHBE	bronchial:	n/a
9	chr9:2239671-2239721	HCF	heart:	n/a
10	chr9:2239671-2239721	CMK	blood:	n/a
11	chr9:2242468-2242518	HAEpiC	amniotic membrane:	n/a
12	chr9:2241688-2241738	LNCaP	prostate:	n/a
13	chr9:2234921-2234971	GM12892	blood:	n/a
14	chr9:2242468-2242518	GM06990	blood:	n/a
15	chr9:2277780-2277830	GM19239	blood:	n/a
16	chr9:2241256-2241306	SAEC	small airway:	n/a
17	chr9:2239671-2239721	SK-N-SH	brain:	n/a
18	chr9:2241688-2241738	BJ	skin:	n/a
19	chr9:2239671-2239721	PANC-1	pancreas:	n/a
20	chr9:2241256-2241306	A549	lung:	n/a
21	chr9:2242468-2242518	NHDF-neo	bronchial:	n/a
22	chr9:2277780-2277830	HRE	kidney:	n/a
23	chr9:2242468-2242518	HRE	kidney:	n/a
24	chr9:2241256-2241306	PrEC	prostate:	n/a
25	chr9:2241892-2241942	AG10803	skin:	n/a
26	chr9:2241688-2241738	NH-A	brain:	n/a
27	chr9:2277780-2277830	NHBE	bronchial:	n/a
28	chr9:2239671-2239721	HIPEpiC	eye:	n/a
29	chr9:2241256-2241306	HUVEC	blood vessel:	n/a
30	chr9:2276469-2276519	GM06990	blood:	n/a
31	chr9:2241892-2241942	SAEC	small airway:	n/a
32	chr9:2276469-2276519	HUVEC	blood vessel:	n/a
33	chr9:2285850-2285900	RPTEC	kidney:	n/a
34	chr9:2276469-2276519	HCT-116	colon:	n/a
35	chr9:2241688-2241738	NT2-D1	testis:	n/a
36	chr9:2234921-2234971	GM06990	blood:	n/a
37	chr9:2241256-2241306	AG04449	skin:	fetal
38	chr9:2285850-2285900	NH-A	brain:	n/a
39	chr9:2234921-2234971	HPAEpiC	pulmonary alveolar:	n/a
40	chr9:2277780-2277830	PANC-1	pancreas:	n/a
41	chr9:2239671-2239721	HCM	heart:	n/a
42	chr9:2241892-2241942	ECC-1	luminal epithelium:	n/a
43	chr9:2234921-2234971	PrEC	prostate:	n/a
44	chr9:2277780-2277830	HRPEpiC	eye:	n/a
45	chr9:2234921-2234971	GM12878	blood:	n/a
46	chr9:2241688-2241738	HEK293	kidney:	embryo
47	chr9:2241256-2241306	HRE	kidney:	n/a
48	chr9:2234921-2234971	AG04449	skin:	fetal
49	chr9:2239671-2239721	U87	brain:	n/a
50	chr9:2241688-2241738	GM06990	blood:	n/a

(count:34 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:2228114..2228719-chr9:2625246..2626097,2	MCF-7	breast:
2	chr9:2226247..2228750-chr9:2234155..2236078,2	MCF-7	breast:
3	chr9:2232135..2233681-chr9:2242107..2243678,2	MCF-7	breast:
4	chr9:2244966..2246945-chr9:2263682..2266605,2	MCF-7	breast:
5	chr9:2242145..2244162-chr9:2246197..2248614,2	MCF-7	breast:
6	chr9:2256748..2259220-chr9:2292192..2293911,2	MCF-7	breast:
7	chr9:2231807..2233920-chr9:2241447..2243691,2	MCF-7	breast:
8	chr9:2216988..2218532-chr9:2223642..2225471,2	MCF-7	breast:
9	chr9:2291871..2293597-chr9:2622079..2623974,2	MCF-7	breast:
10	chr9:2290959..2293717-chr9:2295989..2299437,4	MCF-7	breast:
11	chr9:2243537..2246838-chr9:2247520..2250621,4	MCF-7	breast:
12	chr9:2229721..2232093-chr9:2241469..2243158,2	MCF-7	breast:
13	chr9:2292225..2294051-chr9:2294141..2297013,2	MCF-7	breast:
14	chr9:2226247..2228750-chr9:2234155..2236078,2	MCF-7	breast:
15	chr9:2290959..2293717-chr9:2295989..2299437,4	MCF-7	breast:
16	chr9:2292225..2294051-chr9:2294141..2297013,2	MCF-7	breast:
17	chr9:2255030..2255773-chr9:2600478..2601011,2	MCF-7	breast:
18	chr9:2217416..2220117-chr9:2231617..2233140,2	MCF-7	breast:
19	chr9:2256748..2259220-chr9:2292192..2293911,2	MCF-7	breast:
20	chr9:2244966..2246945-chr9:2263682..2266605,2	MCF-7	breast:
21	chr9:2243537..2246838-chr9:2247520..2250621,4	MCF-7	breast:
22	chr9:2240721..2243292-chr9:2621569..2623384,2	MCF-7	breast:
23	chr9:2266333..2269283-chr9:2269848..2272589,2	K562	blood:
24	chr9:2266333..2269283-chr9:2269848..2272589,2	K562	blood:
25	chr9:2257367..2260216-chr9:2810940..2813820,2	MCF-7	breast:
26	chr9:2242145..2244162-chr9:2246197..2248614,2	MCF-7	breast:
27	chr9:2229879..2232148-chr9:2238435..2240178,2	K562	blood:
28	chr9:2216988..2218532-chr9:2223642..2225471,2	MCF-7	breast:
29	chr9:2229879..2232148-chr9:2238435..2240178,2	K562	blood:
30	chr9:2229721..2232093-chr9:2241469..2243158,2	MCF-7	breast:
31	chr9:2217416..2220117-chr9:2231617..2233140,2	MCF-7	breast:
32	chr9:2016060..2018467-chr9:2241276..2243249,2	K562	blood:
33	chr9:2232135..2233681-chr9:2242107..2243678,2	MCF-7	breast:
34	chr9:2231807..2233920-chr9:2241447..2243691,2	MCF-7	breast:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SMARCA2-5	chr9:2264485-2264628	NONHSAT129991
2	lnc-KIAA0020-6	chr9:2228963-2229241	NONHSAT129990
3	lnc-SMARCA2-5	chr9:2273475-2274167	NONHSAT129991
4	lnc-SMARCA2-6	chr9:2276007-2276253	NONHSAT129989
5	lnc-SMARCA2-6	chr9:2287708-2288332	NONHSAT129989
6	lnc-SMARCA2-6	chr9:2291976-2293037	NONHSAT129989

No data

Variant related genes	Relation type
RN7SL592P	TF binding region
RN7SL592P	CpG island
ENSG00000147852	chromatin interactions
ENSG00000080503	chromatin interactions
ENSG00000236404	chromatin interactions

Extended variants
information (count: 5123 )
Associated
traits (count: 102 )

Variant overlapped rSNPs/rCNVs (count:5123 , 50 per page) page: 1 2 3 4 5 6 7 ... 103

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs552689853	chr9:2215198-2215199	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs187374059	chr9:2215211-2215212	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs149904199	chr9:2215223-2215224	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs189453525	chr9:2215231-2215232	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs374848464	chr9:2215270-2215271	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs567304166	chr9:2215276-2215277	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs529163910	chr9:2215308-2215309	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs180902777	chr9:2215316-2215317	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs369673484	chr9:2215324-2215325	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs540028023	chr9:2215347-2215348	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs373102699	chr9:2215376-2215377	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs35604346	chr9:2215385-2215386	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs146463000	chr9:2215400-2215401	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs73378757	chr9:2215433-2215434	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs571370302	chr9:2215442-2215443	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs12348623	chr9:2215450-2215451	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs568949953	chr9:2215470-2215471	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs553838356	chr9:2215471-2215472	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs143188844	chr9:2215476-2215477	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs185551327	chr9:2215547-2215548	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs556774926	chr9:2215560-2215561	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs576655051	chr9:2215579-2215580	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs375570243	chr9:2215624-2215625	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs10965222	chr9:2215636-2215637	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs146863901	chr9:2215669-2215670	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs190315492	chr9:2215675-2215676	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs373394272	chr9:2215696-2215697	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs140722296	chr9:2215697-2215698	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs538473893	chr9:2215707-2215708	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs529987578	chr9:2215708-2215709	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs28608943	chr9:2215714-2215715	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs562844555	chr9:2215715-2215716	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs531507155	chr9:2215754-2215755	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs551582493	chr9:2215763-2215764	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs537531757	chr9:2215790-2215791	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs78293528	chr9:2215797-2215798	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs560430152	chr9:2215800-2215801	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs1924487	chr9:2215819-2215820	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs567279819	chr9:2215836-2215837	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs141057717	chr9:2215840-2215841	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs555882101	chr9:2215841-2215842	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs576701209	chr9:2215862-2215863	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs182938838	chr9:2215871-2215872	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs559120708	chr9:2215889-2215890	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs80020326	chr9:2215893-2215894	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs541128412	chr9:2215917-2215918	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs561009445	chr9:2215922-2215923	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs186014736	chr9:2215947-2215948	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs150214649	chr9:2215949-2215950	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs563513518	chr9:2215962-2215963	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:102)

Disease	PMID	Source
Gastric cancer	16715143	CNVD
Glioblastoma multiforme	22286061	CNVD
Esophageal squamous carcinoma	18405350	CNVD
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
Developmental delay	21147756	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Autism	20531469	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
Prostate cancer	18632612	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21858162	CNVD
Renal cell carcinoma	21668985	CNVD
Autism	22495311	CNVD
Esophageal cancer	21851588	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Myelofibrosis	22110671	CNVD
Developmental delay	21373258	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Hepatocellular carcinoma	18803288	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Renal cell carcinoma	21215367	CNVD

Chromatin state (count:1358 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:2191600-2221200	Weak transcription	Gastric	stomach
2	chr9:2209400-2216000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr9:2210400-2215800	Weak transcription	Muscle Satellite Cultured Cells	--
4	chr9:2210600-2219000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr9:2215000-2216000	Weak transcription	Cortex derived primary cultured neurospheres	brain
6	chr9:2215000-2217600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
7	chr9:2215800-2216800	Enhancers	Muscle Satellite Cultured Cells	--
8	chr9:2216000-2216200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr9:2216000-2216400	Enhancers	Cortex derived primary cultured neurospheres	brain
10	chr9:2216000-2217000	Enhancers	HSMM	muscle
11	chr9:2216200-2216800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr9:2216200-2217000	Enhancers	NHEK	skin
13	chr9:2216200-2217600	Enhancers	HMEC	breast
14	chr9:2216600-2217600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr9:2216800-2217600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
16	chr9:2217000-2218200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr9:2217600-2219400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
18	chr9:2219000-2219400	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr9:2219400-2223000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr9:2221200-2223000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
21	chr9:2223000-2223200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
22	chr9:2223000-2223600	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
23	chr9:2223000-2224600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr9:2223200-2228400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
25	chr9:2223600-2240800	Weak transcription	HUES64 Cell Line	embryonic stem cell
26	chr9:2224600-2229400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr9:2225600-2228400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
28	chr9:2226800-2227800	Enhancers	Ovary	ovary
29	chr9:2226800-2229000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr9:2227000-2228000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
31	chr9:2227000-2228000	Enhancers	Osteobl	bone
32	chr9:2227200-2227400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
33	chr9:2227200-2227800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
34	chr9:2227200-2227800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
35	chr9:2227200-2227800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
36	chr9:2227200-2227800	Enhancers	Cortex derived primary cultured neurospheres	brain
37	chr9:2227200-2228000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
38	chr9:2227200-2229200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
39	chr9:2227400-2234400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
40	chr9:2227600-2227800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
41	chr9:2227600-2227800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
42	chr9:2227600-2229400	Enhancers	Pancreas	Pancrea
43	chr9:2227800-2229400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
44	chr9:2227800-2230200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
45	chr9:2227800-2231400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
46	chr9:2227800-2231600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
47	chr9:2227800-2231600	Weak transcription	Ovary	ovary
48	chr9:2227800-2234400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
49	chr9:2228000-2228400	Enhancers	Monocytes-CD14+_RO01746	blood
50	chr9:2228000-2229000	Enhancers	Primary neutrophils fromperipheralblood	blood

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