Variant report

Variant	nsv613615
Chromosome Location	chr9:12830070-12947238
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:12878586-12878650	HepG2	liver:	n/a	n/a
2	BCL3	chr9:12859624-12860315	A549	lung:	n/a	chr9:12859689-12859698
3	CBX3	chr9:12859931-12860438	HCT-116	colon:	n/a	n/a
4	CBX3	chr9:12859803-12860402	HCT-116	colon:	n/a	n/a
5	CEBPB	chr9:12840334-12840637	IMR90	lung:	n/a	chr9:12840495-12840506
6	CEBPB	chr9:12884711-12885012	IMR90	lung:	n/a	n/a
7	CEBPB	chr9:12933878-12934366	HCT-116	colon:	n/a	n/a
8	CEBPB	chr9:12859510-12860395	A549	lung:	n/a	chr9:12859838-12859849 chr9:12860058-12860069 chr9:12860056-12860069 chr9:12860058-12860069
9	CEBPB	chr9:12859656-12860357	IMR90	lung:	n/a	chr9:12859838-12859849 chr9:12860058-12860069 chr9:12860056-12860069 chr9:12860058-12860069
10	CEBPB	chr9:12923707-12924077	IMR90	lung:	n/a	n/a
11	CEBPB	chr9:12859594-12860443	MCF-7	breast:	n/a	chr9:12859838-12859849 chr9:12860058-12860069 chr9:12860056-12860069 chr9:12860058-12860069
12	CEBPB	chr9:12877935-12878825	Hela-S3	cervix:	n/a	n/a
13	CEBPB	chr9:12939943-12940204	HepG2	liver:	n/a	chr9:12940029-12940040
14	CEBPB	chr9:12838439-12838686	IMR90	lung:	n/a	chr9:12838441-12838452 chr9:12838441-12838454
15	CEBPB	chr9:12859646-12860343	A549	lung:	n/a	chr9:12859838-12859849 chr9:12860058-12860069 chr9:12860056-12860069 chr9:12860058-12860069
16	CEBPB	chr9:12859680-12860301	ECC-1	luminal epithelium:	n/a	chr9:12859838-12859849 chr9:12860058-12860069 chr9:12860056-12860069 chr9:12860058-12860069
17	CEBPB	chr9:12889477-12889780	HepG2	liver:	n/a	chr9:12889613-12889624
18	CEBPB	chr9:12846597-12846899	HepG2	liver:	n/a	chr9:12846770-12846781 chr9:12846770-12846779
19	CEBPB	chr9:12859688-12860309	MCF-7	breast:	n/a	chr9:12859838-12859849 chr9:12860058-12860069 chr9:12860056-12860069 chr9:12860058-12860069
20	CEBPB	chr9:12889546-12889695	A549	lung:	n/a	chr9:12889613-12889624
21	CEBPB	chr9:12887166-12887433	IMR90	lung:	n/a	n/a
22	CEBPB	chr9:12859687-12860267	ECC-1	luminal epithelium:	n/a	chr9:12859838-12859849 chr9:12860058-12860069 chr9:12860056-12860069 chr9:12860058-12860069
23	CEBPB	chr9:12840343-12840635	A549	lung:	n/a	chr9:12840495-12840506
24	CEBPB	chr9:12859583-12860478	HCT-116	colon:	n/a	chr9:12859838-12859849 chr9:12860058-12860069 chr9:12860056-12860069 chr9:12860058-12860069
25	CEBPB	chr9:12884687-12885143	Hela-S3	cervix:	n/a	n/a
26	CEBPB	chr9:12916032-12916302	H1-hESC	embryonic stem cell:	n/a	n/a
27	CEBPB	chr9:12846628-12846905	IMR90	lung:	n/a	chr9:12846770-12846781 chr9:12846770-12846779
28	CEBPB	chr9:12840351-12840572	HepG2	liver:	n/a	chr9:12840495-12840506
29	CEBPB	chr9:12859348-12860406	Hela-S3	cervix:	n/a	chr9:12859838-12859849 chr9:12860058-12860069 chr9:12860056-12860069 chr9:12860058-12860069
30	CEBPB	chr9:12859513-12860549	HCT-116	colon:	n/a	chr9:12859838-12859849 chr9:12860058-12860069 chr9:12860056-12860069 chr9:12860058-12860069
31	CEBPB	chr9:12939987-12940115	A549	lung:	n/a	chr9:12940029-12940040
32	CEBPB	chr9:12859756-12859967	HepG2	liver:	n/a	chr9:12859838-12859849
33	CEBPB	chr9:12838481-12838483	A549	lung:	n/a	n/a
34	CEBPB	chr9:12859689-12860388	A549	lung:	n/a	chr9:12859838-12859849 chr9:12860058-12860069 chr9:12860056-12860069 chr9:12860058-12860069
35	CHD1	chr9:12884646-12885406	IMR90	lung:	n/a	n/a
36	CHD2	chr9:12856717-12857013	H1-hESC	embryonic stem cell:	n/a	n/a
37	CHD2	chr9:12859665-12860352	Hela-S3	cervix:	n/a	n/a
38	CREB1	chr9:12923756-12923942	A549	lung:	n/a	n/a
39	CTCF	chr9:12890042-12890117	LNCaP	prostate:	n/a	n/a
40	CTCF	chr9:12922300-12922450	NHDF-neo	bronchial:	n/a	chr9:12922395-12922411
41	CTCF	chr9:12884760-12884910	A549	lung:	n/a	n/a
42	CTCF	chr9:12884900-12885050	Hela-S3	cervix:	n/a	n/a
43	CTCF	chr9:12884900-12885050	BJ	skin:	n/a	n/a
44	CTCF	chr9:12884900-12885050	HMF	breast:	n/a	n/a
45	CTCF	chr9:12884880-12885030	AG10803	skin:	n/a	n/a
46	CTCF	chr9:12884900-12885050	AoAF	blood vessel:	n/a	n/a
47	CTCF	chr9:12884940-12885090	HCPEpiC	choroid plexus:	n/a	n/a
48	CTCF	chr9:12884871-12885072	Lung_OC	lung:	n/a	n/a
49	CTCF	chr9:12884880-12885030	AG09319	gingival:	n/a	n/a
50	CTCF	chr9:12836265-12836318	ProgFib	skin:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr9:12899416..12902094-chr9:12902692..12905331,3	MCF-7	breast:
2	chr9:12774887..12777356-chr9:12828580..12830955,2	MCF-7	breast:
3	chr9:12843895..12846216-chr9:12850267..12852861,2	MCF-7	breast:
4	chr9:12779288..12781566-chr9:12835012..12836710,2	MCF-7	breast:
5	chr9:12775378..12777907-chr9:12885456..12887911,2	MCF-7	breast:
6	chr9:12815854..12818984-chr9:12830927..12834079,3	MCF-7	breast:
7	chr9:12827106..12828811-chr9:12846763..12849036,2	MCF-7	breast:
8	chr9:12774893..12776821-chr9:12883465..12885141,2	MCF-7	breast:
9	chr9:12849521..12851462-chr9:12857711..12860176,2	MCF-7	breast:
10	chr9:12776937..12779598-chr9:12883479..12885184,2	MCF-7	breast:
11	chr9:12883524..12885050-chr9:12887759..12890204,2	MCF-7	breast:
12	chr9:12922589..12925309-chr9:12932316..12933934,2	MCF-7	breast:
13	chr3:21274702..21276486-chr9:12852043..12854335,2	MCF-7	breast:
14	chr9:12817203..12820022-chr9:12879979..12881998,2	MCF-7	breast:
15	chr9:12774993..12776787-chr9:12859999..12861752,2	MCF-7	breast:
16	chr9:12899416..12902094-chr9:12902692..12905331,3	MCF-7	breast:
17	chr9:12833643..12836403-chr9:12844199..12845787,2	MCF-7	breast:
18	chr9:12719062..12719862-chr9:12884578..12885277,2	MCF-7	breast:
19	chr9:12778616..12780365-chr9:12854007..12856066,2	MCF-7	breast:
20	chr9:12783262..12785196-chr9:12857512..12860310,2	MCF-7	breast:
21	chr9:12849521..12851462-chr9:12857711..12860176,2	MCF-7	breast:
22	chr9:12776291..12778540-chr9:12858744..12861808,3	MCF-7	breast:
23	chr9:12775552..12777310-chr9:12848376..12849976,2	MCF-7	breast:
24	chr9:12843895..12846216-chr9:12850267..12852861,2	MCF-7	breast:
25	chr9:12851201..12854512-chr9:12857301..12860029,3	MCF-7	breast:
26	chr9:12833643..12836403-chr9:12844199..12845787,2	MCF-7	breast:
27	chr9:12851201..12854512-chr9:12857301..12860029,3	MCF-7	breast:
28	chr9:12774954..12777056-chr9:12883374..12886318,3	MCF-7	breast:
29	chr9:12773830..12776093-chr9:12831481..12833601,2	MCF-7	breast:
30	chr9:12883524..12885050-chr9:12887759..12890204,2	MCF-7	breast:
31	chr9:12922589..12925309-chr9:12932316..12933934,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000222658	TF binding region
ENSG00000153714	chromatin interactions

Extended variants
information (count: 5844 )
Associated
traits (count: 101 )

Variant overlapped rSNPs/rCNVs (count:5844 , 50 per page) page: 1 2 3 4 5 6 7 ... 117

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs617572	chr9:12830070-12830071	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs529729090	chr9:12830094-12830095	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs546723963	chr9:12830136-12830137	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs566432326	chr9:12830142-12830143	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs532132886	chr9:12830162-12830163	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs529183836	chr9:12830170-12830171	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs149986576	chr9:12830184-12830185	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs569032374	chr9:12830196-12830197	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs538173841	chr9:12830204-12830205	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs185919494	chr9:12830221-12830222	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs188377458	chr9:12830279-12830280	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs147678456	chr9:12830284-12830285	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs553041410	chr9:12830307-12830308	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs573048115	chr9:12830336-12830337	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs544981805	chr9:12830355-12830356	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs142432542	chr9:12830364-12830365	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs575816212	chr9:12830377-12830378	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs544913770	chr9:12830387-12830388	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs546789083	chr9:12830397-12830398	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs181201332	chr9:12830403-12830404	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs577283671	chr9:12830406-12830407	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs530328158	chr9:12830431-12830432	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs540867304	chr9:12830441-12830442	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs62538765	chr9:12830462-12830463	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs146611512	chr9:12830473-12830474	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs186751776	chr9:12830483-12830484	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs190743610	chr9:12830494-12830495	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs75527376	chr9:12830529-12830530	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs369398515	chr9:12830539-12830540	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs531478670	chr9:12830572-12830573	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs548467515	chr9:12830606-12830607	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs181026728	chr9:12830640-12830641	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs533735309	chr9:12830652-12830653	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs187102426	chr9:12830654-12830655	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs191124105	chr9:12830670-12830671	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs481063	chr9:12830732-12830733	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs182916710	chr9:12830757-12830758	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs538117444	chr9:12830768-12830769	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs555232067	chr9:12830799-12830800	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs147820364	chr9:12830803-12830804	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs148880876	chr9:12830821-12830822	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs113496439	chr9:12830825-12830826	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs540806034	chr9:12830828-12830829	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs537804784	chr9:12830833-12830834	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs117976301	chr9:12830855-12830856	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs143589363	chr9:12830857-12830858	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs187545346	chr9:12830860-12830861	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs190060258	chr9:12830906-12830907	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs116534228	chr9:12830941-12830942	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs561995098	chr9:12830945-12830946	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:101)

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
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:715 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:12816200-12832000	Weak transcription	HSMMtube	muscle
2	chr9:12819800-12831400	Weak transcription	Fetal Intestine Small	intestine
3	chr9:12820000-12830600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
4	chr9:12825400-12842600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr9:12827000-12837400	Weak transcription	Aorta	Aorta
6	chr9:12830600-12832000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
7	chr9:12831400-12832200	Enhancers	Fetal Intestine Small	intestine
8	chr9:12832000-12834800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
9	chr9:12834800-12835000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
10	chr9:12836400-12840000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr9:12838200-12839000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
12	chr9:12838400-12838800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
13	chr9:12840000-12840800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
14	chr9:12843400-12844200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
15	chr9:12843600-12844600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
16	chr9:12843800-12844000	Enhancers	Colon Smooth Muscle	Colon
17	chr9:12844600-12849400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
18	chr9:12846000-12846600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
19	chr9:12846000-12846800	Enhancers	NHDF-Ad	bronchial
20	chr9:12846200-12846800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr9:12846200-12847000	Enhancers	Fetal Intestine Large	intestine
22	chr9:12846200-12849800	Weak transcription	Colon Smooth Muscle	Colon
23	chr9:12846600-12847600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
24	chr9:12846800-12850200	Weak transcription	NHDF-Ad	bronchial
25	chr9:12846800-12851200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
26	chr9:12847000-12848000	Weak transcription	Fetal Intestine Large	intestine
27	chr9:12847600-12847800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr9:12847600-12847800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr9:12847600-12847800	Enhancers	Pancreatic Islets	Pancreatic Islet
30	chr9:12847800-12850600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr9:12848000-12848800	Enhancers	Fetal Intestine Large	intestine
32	chr9:12848200-12848800	Enhancers	Fetal Intestine Small	intestine
33	chr9:12848800-12849800	Weak transcription	Fetal Intestine Large	intestine
34	chr9:12848800-12849800	Weak transcription	Fetal Intestine Small	intestine
35	chr9:12849400-12850200	Enhancers	Pancreatic Islets	Pancreatic Islet
36	chr9:12849400-12850600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
37	chr9:12849400-12852000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
38	chr9:12849800-12850000	Enhancers	Fetal Kidney	kidney
39	chr9:12849800-12850000	Enhancers	Sigmoid Colon	Sigmoid Colon
40	chr9:12849800-12850200	Enhancers	Colon Smooth Muscle	Colon
41	chr9:12849800-12850400	Enhancers	Fetal Intestine Large	intestine
42	chr9:12849800-12850600	Enhancers	Fetal Intestine Small	intestine
43	chr9:12849800-12851000	Enhancers	Fetal Stomach	stomach
44	chr9:12849800-12851000	Enhancers	Stomach Mucosa	stomach
45	chr9:12849800-12851200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
46	chr9:12849800-12851800	Enhancers	Breast Myoepithelial Primary Cells	Breast
47	chr9:12850000-12850800	Enhancers	Rectal Mucosa Donor 31	rectum
48	chr9:12850000-12851600	Weak transcription	Sigmoid Colon	Sigmoid Colon
49	chr9:12850200-12850400	Enhancers	Small Intestine	intestine
50	chr9:12850200-12851200	Enhancers	NHDF-Ad	bronchial

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links