Variant report

Variant	nsv1023816
Chromosome Location	chr9:13008542-13064793
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:483)
CpG islands
(count:61)
Chromatin interactive
region (count:21)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:483 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:13034076-13034447	HepG2	liver:	n/a	n/a
2	CEBPB	chr9:13023407-13023862	MCF-7	breast:	n/a	chr9:13023441-13023452
3	CEBPB	chr9:13017938-13018130	HepG2	liver:	n/a	n/a
4	CEBPB	chr9:13022910-13023041	A549	lung:	n/a	n/a
5	CEBPB	chr9:13017970-13018214	A549	lung:	n/a	n/a
6	CEBPB	chr9:13064015-13064567	MCF-7	breast:	n/a	n/a
7	CEBPB	chr9:13023462-13023889	MCF-7	breast:	n/a	n/a
8	CHD2	chr9:13034283-13034375	HepG2	liver:	n/a	n/a
9	CREB1	chr9:13034239-13034529	A549	lung:	n/a	n/a
10	CTCF	chr9:13034256-13034505	H1-hESC	embryonic stem cell:	n/a	n/a
11	CTCF	chr9:13056860-13056984	H1-hESC	embryonic stem cell:	n/a	n/a
12	CTCF	chr9:13034280-13034430	MCF-7	breast:	n/a	n/a
13	CTCF	chr9:13034171-13034492	K562	blood:	n/a	n/a
14	CTCF	chr9:13034280-13034430	BE2_C	brain:	n/a	n/a
15	CTCF	chr9:13034280-13034430	RPTEC	kidney:	n/a	n/a
16	CTCF	chr9:13030540-13030690	WI-38	lung:	n/a	n/a
17	CTCF	chr9:13034340-13034490	GM12868	blood:	n/a	n/a
18	CTCF	chr9:13034300-13034450	GM12871	blood:	n/a	n/a
19	CTCF	chr9:13034300-13034450	HCFaa	heart:	n/a	n/a
20	CTCF	chr9:13034135-13034596	IMR90	lung:	n/a	n/a
21	CTCF	chr9:13034242-13034528	MCF-7	breast:	n/a	n/a
22	CTCF	chr9:13034236-13034526	SK-N-SH_RA	brain:	n/a	n/a
23	CTCF	chr9:13056893-13056944	GM12891	blood:	n/a	n/a
24	CTCF	chr9:13034262-13034483	GM19240	blood:	n/a	n/a
25	CTCF	chr9:13034300-13034450	HUVEC	blood vessel:	n/a	n/a
26	CTCF	chr9:13054388-13054420	Lung_OC	lung:	n/a	n/a
27	CTCF	chr9:13034240-13034390	WI-38	lung:	n/a	n/a
28	CTCF	chr9:13034167-13034505	K562	blood:	n/a	n/a
29	CTCF	chr9:13034260-13034410	HA-sp	spinal cord:	n/a	n/a
30	CTCF	chr9:13034280-13034430	GM06990	blood:	n/a	n/a
31	CTCF	chr9:13034261-13034496	SK-N-SH_RA	brain:	n/a	n/a
32	CTCF	chr9:13034142-13034632	MCF-7	breast:	n/a	n/a
33	CTCF	chr9:13034226-13034494	LNCaP	prostate:	n/a	n/a
34	CTCF	chr9:13034300-13034450	GM12801	blood:	n/a	n/a
35	CTCF	chr9:13034236-13034506	K562	blood:	n/a	n/a
36	CTCF	chr9:13034340-13034490	GM12864	blood:	n/a	n/a
37	CTCF	chr9:13034300-13034450	HEEpiC	esophagus:	n/a	n/a
38	CTCF	chr9:13034260-13034410	GM12865	blood:	n/a	n/a
39	CTCF	chr9:13034320-13034470	HCT-116	colon:	n/a	n/a
40	CTCF	chr9:13034340-13034490	WERI-Rb-1	eye:	n/a	n/a
41	CTCF	chr9:13034340-13034490	GM12869	blood:	n/a	n/a
42	CTCF	chr9:13034320-13034470	NHLF	lung:	n/a	n/a
43	CTCF	chr9:13034235-13034505	Hela-S3	cervix:	n/a	n/a
44	CTCF	chr9:13034300-13034450	Caco-2	colon:	n/a	n/a
45	CTCF	chr9:13034193-13034575	HepG2	liver:	n/a	n/a
46	CTCF	chr9:13034320-13034470	MCF-7	breast:	n/a	n/a
47	CTCF	chr9:13034133-13034560	H1-hESC	embryonic stem cell:	n/a	n/a
48	CTCF	chr9:13034260-13034410	HCM	heart:	n/a	n/a
49	CTCF	chr9:13056740-13056890	A549	lung:	n/a	n/a
50	CTCF	chr9:13034300-13034450	HPAF	blood vessel:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:13038210-13038260	NHBE	bronchial:	n/a
2	chr9:13038210-13038260	AG09309	skin:	n/a
3	chr9:13038210-13038260	K562	blood:	n/a
4	chr9:13038210-13038260	MCF10A-Er-Src	breast:	n/a
5	chr9:13038210-13038260	RPTEC	kidney:	n/a
6	chr9:13038210-13038260	CMK	blood:	n/a
7	chr9:13038210-13038260	HAEpiC	amniotic membrane:	n/a
8	chr9:13038210-13038260	PFSK-1	brain:	n/a
9	chr9:13038210-13038260	AoSMC	blood vessel:	n/a
10	chr9:13038210-13038260	SK-N-SH_RA	brain:	n/a
11	chr9:13038210-13038260	BE2_C	brain:	n/a
12	chr9:13038210-13038260	GM12878	blood:	n/a
13	chr9:13038210-13038260	HCPEpiC	choroid plexus:	n/a
14	chr9:13038210-13038260	HL-60	blood:	n/a
15	chr9:13038210-13038260	HRE	kidney:	n/a
16	chr9:13038210-13038260	BJ	skin:	n/a
17	chr9:13038210-13038260	SK-N-MC	brain:	n/a
18	chr9:13038210-13038260	Hepatocyte	liver:	n/a
19	chr9:13038210-13038260	HRCEpiC	kidney:	n/a
20	chr9:13038210-13038260	PANC-1	pancreas:	n/a
21	chr9:13038210-13038260	MCF-7	breast:	n/a
22	chr9:13038210-13038260	HMEC	breast:	n/a
23	chr9:13038210-13038260	AG10803	skin:	n/a
24	chr9:13038210-13038260	ProgFib	skin:	n/a
25	chr9:13038210-13038260	NHDF-neo	bronchial:	n/a
26	chr9:13038210-13038260	GM19239	blood:	n/a
27	chr9:13038210-13038260	SAEC	small airway:	n/a
28	chr9:13038210-13038260	SK-N-SH	brain:	n/a
29	chr9:13038210-13038260	NB4	blood:	n/a
30	chr9:13038210-13038260	U87	brain:	n/a
31	chr9:13038210-13038260	GM12891	blood:	n/a
32	chr9:13038210-13038260	HEEpiC	esophagus:	n/a
33	chr9:13038210-13038260	HIPEpiC	eye:	n/a
34	chr9:13038210-13038260	HNPCEpiC	eye:	n/a
35	chr9:13038210-13038260	HEK293	kidney:	embryo
36	chr9:13038210-13038260	Jurkat	blood:	n/a
37	chr9:13038210-13038260	Hela-S3	cervix:	n/a
38	chr9:13038210-13038260	HRPEpiC	eye:	n/a
39	chr9:13038210-13038260	NT2-D1	testis:	n/a
40	chr9:13038210-13038260	H1-hESC	embryonic stem cell:	embryo
41	chr9:13038210-13038260	Caco-2	colon:	n/a
42	chr9:13038210-13038260	HepG2	liver:	n/a
43	chr9:13038210-13038260	HCT-116	colon:	n/a
44	chr9:13038210-13038260	AG09319	gingival:	n/a
45	chr9:13038210-13038260	HCM	heart:	n/a
46	chr9:13038210-13038260	SKMC	muscle:	n/a
47	chr9:13038210-13038260	GM06990	blood:	n/a
48	chr9:13038210-13038260	AG04450	lung:	fetal
49	chr9:13038210-13038260	HUVEC	blood vessel:	n/a
50	chr9:13038210-13038260	IMR90	lung:	fetal

(count:21 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:13044695..13047159-chr9:13050621..13052940,2	K562	blood:
2	chr9:13020387..13022064-chr9:13024360..13026782,2	K562	blood:
3	chr9:13058767..13060767-chr9:13068798..13070825,2	MCF-7	breast:
4	chr9:13050118..13051990-chr9:13062072..13064345,2	MCF-7	breast:
5	chr9:13033734..13035793-chr9:13280439..13283221,2	K562	blood:
6	chr9:13008470..13010567-chr9:13018005..13020586,2	MCF-7	breast:
7	chr9:13013683..13015999-chr9:13017070..13019514,2	MCF-7	breast:
8	chr9:13046311..13049119-chr9:13049415..13051985,2	MCF-7	breast:
9	chr9:13033929..13034651-chr9:14400323..14400953,2	MCF-7	breast:
10	chr9:13046311..13049119-chr9:13049415..13051985,2	MCF-7	breast:
11	chr9:13034942..13035837-chr9:13088355..13089237,4	MCF-7	breast:
12	chr9:13013683..13015999-chr9:13017070..13019514,2	MCF-7	breast:
13	chr9:13056729..13057438-chr9:13089019..13089759,2	MCF-7	breast:
14	chr9:13008470..13010567-chr9:13018005..13020586,2	MCF-7	breast:
15	chr9:13044695..13047159-chr9:13050621..13052940,2	K562	blood:
16	chr9:13033916..13034844-chr9:13088403..13089550,10	MCF-7	breast:
17	chr9:13050118..13051990-chr9:13062072..13064345,2	MCF-7	breast:
18	chr9:13034030..13034837-chr9:13088503..13089360,4	K562	blood:
19	chr9:13033933..13036265-chr9:13080318..13084279,3	MCF-7	breast:
20	chr9:13020387..13022064-chr9:13024360..13026782,2	K562	blood:
21	chr9:13036362..13039283-chr9:13086631..13088810,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MPDZ-4	chr9:13021693-13022891	NONHSAT130232

No data

Variant related genes	Relation type
ENSG00000234586	TF binding region
ENSG00000234586	CpG island

Extended variants
information (count: 1591 )
Associated
traits (count: 104 )

Variant overlapped rSNPs/rCNVs (count:1591 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs150587953	chr9:13009816-13009817	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs556814976	chr9:13009972-13009973	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs554093573	chr9:13009991-13009992	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs566943850	chr9:13010039-13010040	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs570480663	chr9:13010050-13010051	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs35507733	chr9:13010053-13010054	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs558375841	chr9:13010070-13010071	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs1412304	chr9:13010074-13010075	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs375974738	chr9:13010121-13010122	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs12345742	chr9:13010123-13010124	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs555842353	chr9:13010136-13010137	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs372569706	chr9:13010140-13010141	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs12345688	chr9:13010170-13010171	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs139646378	chr9:13010182-13010183	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs1412303	chr9:13010191-13010192	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs537155682	chr9:13013635-13013636	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs2183136	chr9:13013636-13013637	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs567698443	chr9:13013686-13013687	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs114353588	chr9:13013689-13013690	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs73402331	chr9:13013702-13013703	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs35311996	chr9:13013722-13013723	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs377507549	chr9:13013777-13013778	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs534120306	chr9:13013790-13013791	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs573467559	chr9:13013795-13013796	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs562295172	chr9:13013847-13013848	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs539188567	chr9:13013875-13013876	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs141874783	chr9:13013879-13013880	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs575373932	chr9:13013883-13013884	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs182269610	chr9:13013891-13013892	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs550313104	chr9:13013892-13013893	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs560697308	chr9:13013936-13013937	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs10738310	chr9:13013990-13013991	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs539859425	chr9:13013991-13013992	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs12001424	chr9:13014011-13014012	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs532297813	chr9:13014146-13014147	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs79348563	chr9:13014151-13014152	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs562378521	chr9:13014157-13014158	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs372601600	chr9:13014158-13014159	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs530891218	chr9:13014170-13014171	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs551101650	chr9:13014179-13014180	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs10124215	chr9:13014225-13014226	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs10756439	chr9:13014232-13014233	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs546679685	chr9:13014236-13014237	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs564053648	chr9:13014247-13014248	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs113684567	chr9:13014255-13014256	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs538229723	chr9:13014263-13014264	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs114990661	chr9:13014335-13014336	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs552319347	chr9:13014346-13014347	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs186976718	chr9:13014358-13014359	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs569497822	chr9:13014361-13014362	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:104)

Disease	PMID	Source
Disorders of sex development	21048976	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
Chronic lymphocytic leukemia	21546498	CNVD
abnormal development	18461090	CNVD
Glioblastoma multiforme	21080181	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
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Lung cancer	18438408	CNVD
Urothelial carcinoma	21177765	CNVD
Oral cancer	21386901	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	21785460	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21858162	CNVD
Renal cell carcinoma	21668985	CNVD
Myelodysplastic syndrome	21251322	CNVD
Autism	22495311	CNVD
Hepatocellular carcinoma	18803288	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma	19074898	CNVD
Malignant melanoma	19074898	CNVD
Prostate cancer	16573809	CNVD
Metanephric adenoma	20802469	CNVD
Developmental delay	21147756	CNVD
small cell lung cancer	21764851	CNVD
Glioblastoma multiforme	22286061	CNVD
Glioma	17123091	CNVD
Lung cancer	16773561	CNVD
Colorectal cancer	16272173	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Gastric cancer	16891809	CNVD
Mental retardation	17847001	CNVD
Cutaneous squamous cell carcinomas	17420988	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Pilocytic astrocytoma	18670637	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Melanoma	22183965	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Breast cancer	21611746	CNVD
Breast cancer	22522925	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Renal cell carcinoma	21215367	CNVD
Chordoma	21215367	CNVD

Chromatin state (count:261 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:13009800-13010200	Enhancers	Fetal Heart	heart
2	chr9:13013600-13014400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
3	chr9:13013600-13015000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
4	chr9:13014000-13014400	Enhancers	HUVEC	blood vessel
5	chr9:13014000-13014800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
6	chr9:13014200-13014400	Weak transcription	Fetal Lung	lung
7	chr9:13014200-13014800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr9:13014200-13014800	Enhancers	HSMM	muscle
9	chr9:13014200-13014800	Enhancers	HSMMtube	muscle
10	chr9:13014200-13014800	Enhancers	NH-A	brain
11	chr9:13014200-13014800	Enhancers	Osteobl	bone
12	chr9:13014400-13014600	ZNF genes & repeats	Fetal Lung	lung
13	chr9:13014400-13014800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr9:13014400-13014800	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
15	chr9:13014400-13014800	Enhancers	Muscle Satellite Cultured Cells	--
16	chr9:13014400-13014800	Enhancers	NHDF-Ad	bronchial
17	chr9:13014400-13014800	Enhancers	NHLF	lung
18	chr9:13014600-13014800	Enhancers	Fetal Lung	lung
19	chr9:13014800-13015200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
20	chr9:13014800-13016000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
21	chr9:13014800-13016400	Weak transcription	Fetal Lung	lung
22	chr9:13014800-13020200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
23	chr9:13015200-13020000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
24	chr9:13016200-13016400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
25	chr9:13016400-13017800	Enhancers	Fetal Lung	lung
26	chr9:13017800-13019000	Weak transcription	Fetal Lung	lung
27	chr9:13019000-13019800	Enhancers	Fetal Lung	lung
28	chr9:13019800-13020000	Enhancers	Rectal Smooth Muscle	rectum
29	chr9:13019800-13020800	Flanking Active TSS	Fetal Lung	lung
30	chr9:13020000-13020200	Enhancers	HSMMtube	muscle
31	chr9:13020000-13021000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
32	chr9:13020200-13020400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
33	chr9:13020200-13020400	Flanking Active TSS	HSMMtube	muscle
34	chr9:13020200-13020600	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
35	chr9:13020400-13020800	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
36	chr9:13020400-13020800	Enhancers	Fetal Muscle Leg	muscle
37	chr9:13020400-13020800	Active TSS	HSMMtube	muscle
38	chr9:13020400-13021000	Enhancers	NHLF	lung
39	chr9:13020600-13020800	Enhancers	Rectal Smooth Muscle	rectum
40	chr9:13020600-13021000	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
41	chr9:13020800-13021000	Enhancers	Fetal Lung	lung
42	chr9:13020800-13027000	Weak transcription	HSMMtube	muscle
43	chr9:13021000-13021200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
44	chr9:13021000-13033600	Weak transcription	Fetal Lung	lung
45	chr9:13021600-13022000	Enhancers	HUES64 Cell Line	embryonic stem cell
46	chr9:13021600-13022000	Enhancers	iPS-15b Cell Line	embryonic stem cell
47	chr9:13021600-13022800	Enhancers	ES-I3 Cell Line	embryonic stem cell
48	chr9:13022800-13027400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
49	chr9:13023400-13024000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
50	chr9:13023400-13024200	Enhancers	NHEK	skin

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links