Variant report

Variant	nsv892059
Chromosome Location	chr9:2198627-2255397
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1127)
CpG islands
(count:366)
Chromatin interactive
region (count:25)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1127 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:2241873-2242174	K562	blood:	n/a	n/a
2	ARID3A	chr9:2241752-2242185	HepG2	liver:	n/a	n/a
3	ATF2	chr9:2241795-2242260	GM12878	blood:	n/a	n/a
4	ATF2	chr9:2229314-2229763	GM12878	blood:	n/a	n/a
5	ATF2	chr9:2241526-2242216	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr9:2241499-2242598	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr9:2241813-2242242	GM12878	blood:	n/a	n/a
8	ATF2	chr9:2229291-2229713	GM12878	blood:	n/a	n/a
9	ATF3	chr9:2241780-2242300	A549	lung:	n/a	n/a
10	BACH1	chr9:2214189-2214457	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr9:2241631-2242354	H1-hESC	embryonic stem cell:	n/a	n/a
12	BATF	chr9:2230017-2230285	GM12878	blood:	n/a	chr9:2230183-2230193 chr9:2230182-2230193
13	BCL11A	chr9:2241903-2242115	GM12878	blood:	n/a	n/a
14	BCL3	chr9:2241755-2242399	A549	lung:	n/a	n/a
15	BCL3	chr9:2241690-2242337	A549	lung:	n/a	n/a
16	BCLAF1	chr9:2241766-2242280	GM12878	blood:	n/a	n/a
17	BCLAF1	chr9:2229240-2229763	GM12878	blood:	n/a	chr9:2229561-2229570
18	BCLAF1	chr9:2241790-2242233	GM12878	blood:	n/a	n/a
19	BHLHE40	chr9:2241927-2242471	GM12878	blood:	n/a	n/a
20	BHLHE40	chr9:2241822-2242611	HepG2	liver:	n/a	n/a
21	BHLHE40	chr9:2241630-2242313	K562	blood:	n/a	n/a
22	BHLHE40	chr9:2209457-2209743	K562	blood:	n/a	n/a
23	BHLHE40	chr9:2208494-2208781	K562	blood:	n/a	n/a
24	BRCA1	chr9:2242326-2242348	GM12878	blood:	n/a	n/a
25	BRCA1	chr9:2241818-2242305	H1-hESC	embryonic stem cell:	n/a	n/a
26	CBX3	chr9:2241713-2242381	HCT-116	colon:	n/a	n/a
27	CBX3	chr9:2241820-2242161	K562	blood:	n/a	n/a
28	CBX3	chr9:2241725-2242505	HCT-116	colon:	n/a	n/a
29	CCNT2	chr9:2241616-2242096	K562	blood:	n/a	n/a
30	CCNT2	chr9:2209386-2209592	K562	blood:	n/a	n/a
31	CEBPB	chr9:2228196-2228506	IMR90	lung:	n/a	n/a
32	CEBPB	chr9:2228159-2228502	A549	lung:	n/a	n/a
33	CEBPB	chr9:2209042-2209288	A549	lung:	n/a	chr9:2209143-2209154
34	CEBPB	chr9:2227505-2227839	H1-hESC	embryonic stem cell:	n/a	chr9:2227644-2227655
35	CEBPB	chr9:2228094-2228527	H1-hESC	embryonic stem cell:	n/a	n/a
36	CEBPB	chr9:2209235-2209259	H1-hESC	embryonic stem cell:	n/a	n/a
37	CEBPB	chr9:2244301-2244558	HepG2	liver:	n/a	chr9:2244415-2244426
38	CEBPB	chr9:2228170-2228469	A549	lung:	n/a	n/a
39	CEBPB	chr9:2209012-2209288	HepG2	liver:	n/a	chr9:2209143-2209154
40	CEBPB	chr9:2209006-2209254	K562	blood:	n/a	chr9:2209143-2209154
41	CEBPB	chr9:2217015-2217182	HepG2	liver:	n/a	chr9:2217142-2217153
42	CEBPB	chr9:2241958-2242358	IMR90	lung:	n/a	n/a
43	CEBPB	chr9:2241880-2242260	A549	lung:	n/a	n/a
44	CEBPB	chr9:2228177-2228478	ECC-1	luminal epithelium:	n/a	n/a
45	CEBPB	chr9:2227487-2227843	HepG2	liver:	n/a	chr9:2227644-2227655
46	CEBPB	chr9:2228100-2228461	ECC-1	luminal epithelium:	n/a	n/a
47	CEBPB	chr9:2228058-2228629	HCT-116	colon:	n/a	n/a
48	CEBPB	chr9:2228058-2228601	A549	lung:	n/a	n/a
49	CEBPB	chr9:2227460-2227833	IMR90	lung:	n/a	chr9:2227644-2227655
50	CEBPB	chr9:2227489-2227810	K562	blood:	n/a	chr9:2227644-2227655

(count:366 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:2241892-2241942	ProgFib	skin:	n/a
2	chr9:2239671-2239721	PFSK-1	brain:	n/a
3	chr9:2242468-2242518	AG04449	skin:	fetal
4	chr9:2241892-2241942	HRCEpiC	kidney:	n/a
5	chr9:2234921-2234971	HCT-116	colon:	n/a
6	chr9:2241256-2241306	HUVEC	blood vessel:	n/a
7	chr9:2241892-2241942	HMEC	breast:	n/a
8	chr9:2242468-2242518	HPAEpiC	pulmonary alveolar:	n/a
9	chr9:2241256-2241306	GM12892	blood:	n/a
10	chr9:2242468-2242518	HEK293	kidney:	embryo
11	chr9:2239671-2239721	BE2_C	brain:	n/a
12	chr9:2241892-2241942	A549	lung:	n/a
13	chr9:2241892-2241942	Caco-2	colon:	n/a
14	chr9:2242468-2242518	Caco-2	colon:	n/a
15	chr9:2241688-2241738	Hepatocyte	liver:	n/a
16	chr9:2242468-2242518	NB4	blood:	n/a
17	chr9:2241892-2241942	NH-A	brain:	n/a
18	chr9:2242468-2242518	NT2-D1	testis:	n/a
19	chr9:2239671-2239721	HMEC	breast:	n/a
20	chr9:2241688-2241738	HepG2	liver:	n/a
21	chr9:2242468-2242518	U87	brain:	n/a
22	chr9:2241688-2241738	U87	brain:	n/a
23	chr9:2242468-2242518	HL-60	blood:	n/a
24	chr9:2239671-2239721	ECC-1	luminal epithelium:	n/a
25	chr9:2242468-2242518	HCPEpiC	choroid plexus:	n/a
26	chr9:2242468-2242518	CMK	blood:	n/a
27	chr9:2241688-2241738	LNCaP	prostate:	n/a
28	chr9:2241892-2241942	HCT-116	colon:	n/a
29	chr9:2239671-2239721	HIPEpiC	eye:	n/a
30	chr9:2234921-2234971	IMR90	lung:	fetal
31	chr9:2241892-2241942	PANC-1	pancreas:	n/a
32	chr9:2241892-2241942	HEK293	kidney:	embryo
33	chr9:2242468-2242518	SK-N-SH_RA	brain:	n/a
34	chr9:2241892-2241942	BE2_C	brain:	n/a
35	chr9:2234921-2234971	Jurkat	blood:	n/a
36	chr9:2242468-2242518	A549	lung:	n/a
37	chr9:2241688-2241738	NB4	blood:	n/a
38	chr9:2242468-2242518	MCF10A-Er-Src	breast:	n/a
39	chr9:2241256-2241306	AG09319	gingival:	n/a
40	chr9:2242468-2242518	Hepatocyte	liver:	n/a
41	chr9:2239671-2239721	HRCEpiC	kidney:	n/a
42	chr9:2242468-2242518	HRPEpiC	eye:	n/a
43	chr9:2241892-2241942	U87	brain:	n/a
44	chr9:2242468-2242518	SAEC	small airway:	n/a
45	chr9:2234921-2234971	AoSMC	blood vessel:	n/a
46	chr9:2241892-2241942	HL-60	blood:	n/a
47	chr9:2234921-2234971	Caco-2	colon:	n/a
48	chr9:2241688-2241738	HCT-116	colon:	n/a
49	chr9:2241892-2241942	NT2-D1	testis:	n/a
50	chr9:2241256-2241306	HEEpiC	esophagus:	n/a

(count:25 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:2228114..2228719-chr9:2625246..2626097,2	MCF-7	breast:
2	chr9:2232135..2233681-chr9:2242107..2243678,2	MCF-7	breast:
3	chr9:2231807..2233920-chr9:2241447..2243691,2	MCF-7	breast:
4	chr9:2242145..2244162-chr9:2246197..2248614,2	MCF-7	breast:
5	chr9:2203906..2206427-chr9:2209361..2211517,2	MCF-7	breast:
6	chr9:2229879..2232148-chr9:2238435..2240178,2	K562	blood:
7	chr9:2229721..2232093-chr9:2241469..2243158,2	MCF-7	breast:
8	chr9:2231807..2233920-chr9:2241447..2243691,2	MCF-7	breast:
9	chr9:2232135..2233681-chr9:2242107..2243678,2	MCF-7	breast:
10	chr9:2242145..2244162-chr9:2246197..2248614,2	MCF-7	breast:
11	chr9:2226247..2228750-chr9:2234155..2236078,2	MCF-7	breast:
12	chr9:2229879..2232148-chr9:2238435..2240178,2	K562	blood:
13	chr9:2216988..2218532-chr9:2223642..2225471,2	MCF-7	breast:
14	chr9:2216988..2218532-chr9:2223642..2225471,2	MCF-7	breast:
15	chr9:2203906..2206427-chr9:2209361..2211517,2	MCF-7	breast:
16	chr9:2229721..2232093-chr9:2241469..2243158,2	MCF-7	breast:
17	chr9:2243537..2246838-chr9:2247520..2250621,4	MCF-7	breast:
18	chr9:2243537..2246838-chr9:2247520..2250621,4	MCF-7	breast:
19	chr9:2217416..2220117-chr9:2231617..2233140,2	MCF-7	breast:
20	chr9:2226247..2228750-chr9:2234155..2236078,2	MCF-7	breast:
21	chr9:2217416..2220117-chr9:2231617..2233140,2	MCF-7	breast:
22	chr9:2255030..2255773-chr9:2600478..2601011,2	MCF-7	breast:
23	chr9:2016060..2018467-chr9:2241276..2243249,2	K562	blood:
24	chr9:2244966..2246945-chr9:2263682..2266605,2	MCF-7	breast:
25	chr9:2240721..2243292-chr9:2621569..2623384,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KIAA0020-6	chr9:2228963-2229241	NONHSAT129990
2	lnc-SMARCA2-6	chr9:2213894-2214217	NONHSAT129989

No data

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

Extended variants
information (count: 3357 )
Associated
traits (count: 109 )

Variant overlapped rSNPs/rCNVs (count:3357 , 50 per page) page: 1 2 3 4 5 6 7 ... 68

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10965177	chr9:2198627-2198628	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs538776890	chr9:2198640-2198641	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs543135357	chr9:2198683-2198684	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs553010320	chr9:2198726-2198727	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs562918527	chr9:2198728-2198729	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs531710761	chr9:2198746-2198747	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs142448977	chr9:2198752-2198753	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs143984008	chr9:2198755-2198756	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs12341162	chr9:2198760-2198761	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs546726948	chr9:2198765-2198766	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs148606801	chr9:2198767-2198768	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs115933176	chr9:2198787-2198788	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs548663149	chr9:2198788-2198789	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs371562148	chr9:2198792-2198793	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs12345888	chr9:2198823-2198824	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs537861351	chr9:2198829-2198830	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs537829526	chr9:2198836-2198837	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs76427022	chr9:2198839-2198840	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs542899629	chr9:2198840-2198841	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs74997159	chr9:2198868-2198869	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs149754130	chr9:2198871-2198872	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs534140700	chr9:2198874-2198875	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs554448825	chr9:2198875-2198876	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs374602382	chr9:2198906-2198907	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs7020200	chr9:2198916-2198917	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs142081400	chr9:2198917-2198918	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs576374860	chr9:2198932-2198933	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs572104542	chr9:2198947-2198948	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs184399349	chr9:2198988-2198989	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs564226525	chr9:2198996-2198997	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs113499183	chr9:2199041-2199042	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs541069131	chr9:2199052-2199053	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs150895682	chr9:2199063-2199064	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs540125482	chr9:2199066-2199067	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs74344027	chr9:2199070-2199071	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs529030577	chr9:2199085-2199086	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs140213908	chr9:2199093-2199094	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs16937942	chr9:2199102-2199103	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs374177886	chr9:2199110-2199111	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs548700243	chr9:2199116-2199117	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs540893778	chr9:2199135-2199136	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs554440389	chr9:2199140-2199141	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs115586310	chr9:2199167-2199168	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs531214584	chr9:2199201-2199202	ZNF genes & repeats Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs577489788	chr9:2199205-2199206	ZNF genes & repeats Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs551099377	chr9:2199216-2199217	ZNF genes & repeats Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs374716564	chr9:2199223-2199224	ZNF genes & repeats Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs189721257	chr9:2199234-2199235	ZNF genes & repeats Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs115539876	chr9:2199265-2199266	ZNF genes & repeats Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs181209221	chr9:2199266-2199267	ZNF genes & repeats Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:109)

Disease	PMID	Source
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
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
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
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
Peripheral t-cell lymphoma	19118030	CNVD
Developmental delay	21373258	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Hepatocellular carcinoma	18803288	CNVD
Chordoma	21215367	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Schizophrenia	23813976	CNVD

Chromatin state (count:991 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:2173200-2201800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr9:2179400-2202800	Weak transcription	Psoas Muscle	Psoas
3	chr9:2180800-2198800	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
4	chr9:2181600-2198800	Strong transcription	Primary T helper cells fromperipheralblood	blood
5	chr9:2181600-2199200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr9:2181600-2199400	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
7	chr9:2182400-2199200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
8	chr9:2188000-2201600	Weak transcription	Small Intestine	intestine
9	chr9:2188400-2202400	Strong transcription	Primary T cells from cord blood	blood
10	chr9:2189000-2199000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
11	chr9:2191600-2213800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
12	chr9:2191600-2221200	Weak transcription	Gastric	stomach
13	chr9:2192000-2199200	Weak transcription	HUVEC	blood vessel
14	chr9:2192200-2199800	Weak transcription	Colonic Mucosa	Colon
15	chr9:2192200-2200000	Weak transcription	Fetal Intestine Small	intestine
16	chr9:2192200-2200000	Weak transcription	Pancreas	Pancrea
17	chr9:2192200-2200200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr9:2192800-2202400	Weak transcription	Colon Smooth Muscle	Colon
19	chr9:2193000-2199200	Weak transcription	HUES48 Cell Line	embryonic stem cell
20	chr9:2193200-2200400	Weak transcription	Brain Inferior Temporal Lobe	brain
21	chr9:2193200-2200400	Weak transcription	Fetal Lung	lung
22	chr9:2193200-2208600	Weak transcription	Placenta Amnion	Placenta Amnion
23	chr9:2193600-2198800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
24	chr9:2194000-2199000	Weak transcription	Fetal Brain Female	brain
25	chr9:2194000-2199200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr9:2194000-2202200	Weak transcription	Cortex derived primary cultured neurospheres	brain
27	chr9:2194200-2203000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
28	chr9:2194200-2203200	Weak transcription	Rectal Mucosa Donor 29	rectum
29	chr9:2194800-2199000	Weak transcription	Fetal Thymus	thymus
30	chr9:2195200-2199200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
31	chr9:2195200-2199400	Weak transcription	HUES6 Cell Line	embryonic stem cell
32	chr9:2195200-2199400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
33	chr9:2195800-2201800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
34	chr9:2196000-2198800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
35	chr9:2196000-2199800	Weak transcription	Placenta	Placenta
36	chr9:2196000-2200000	Weak transcription	Lung	lung
37	chr9:2196000-2200200	Weak transcription	Spleen	Spleen
38	chr9:2196000-2200400	Weak transcription	Ovary	ovary
39	chr9:2196000-2200400	Weak transcription	Right Ventricle	heart
40	chr9:2196000-2203200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
41	chr9:2196200-2199200	Weak transcription	Adipose Nuclei	Adipose
42	chr9:2196200-2200400	Weak transcription	Esophagus	oesophagus
43	chr9:2196200-2200600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
44	chr9:2196200-2200600	Weak transcription	Dnd41	blood
45	chr9:2196400-2199400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
46	chr9:2196400-2199400	Weak transcription	Rectal Smooth Muscle	rectum
47	chr9:2196400-2199800	Weak transcription	Fetal Muscle Leg	muscle
48	chr9:2196400-2200000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
49	chr9:2196400-2200000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
50	chr9:2196400-2200000	Weak transcription	Aorta	Aorta

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