Variant report

Variant	nsv892050
Chromosome Location	chr9:1928694-1992516
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	ATF2	chr9:1929571-1930870	GM12878	blood:	n/a	n/a
2	ATF2	chr9:1939474-1940442	GM12878	blood:	n/a	n/a
3	ATF2	chr9:1938015-1939279	GM12878	blood:	n/a	n/a
4	ATF2	chr9:1929686-1930864	GM12878	blood:	n/a	n/a
5	ATF2	chr9:1938043-1940564	GM12878	blood:	n/a	n/a
6	ATF2	chr9:1929153-1929564	GM12878	blood:	n/a	n/a
7	ATF3	chr9:1930434-1930758	GM12878	blood:	n/a	chr9:1930664-1930684
8	BATF	chr9:1929707-1930264	GM12878	blood:	n/a	n/a
9	BATF	chr9:1982196-1982410	GM12878	blood:	n/a	n/a
10	BATF	chr9:1943777-1944045	GM12878	blood:	n/a	chr9:1943972-1943982 chr9:1943968-1943978
11	BATF	chr9:1940040-1940444	GM12878	blood:	n/a	n/a
12	BATF	chr9:1929690-1930695	GM12878	blood:	n/a	n/a
13	BATF	chr9:1938070-1939174	GM12878	blood:	n/a	n/a
14	BCL11A	chr9:1982176-1982424	GM12878	blood:	n/a	n/a
15	BCL11A	chr9:1930282-1930570	GM12878	blood:	n/a	n/a
16	BCL11A	chr9:1982181-1982398	GM12878	blood:	n/a	n/a
17	BCL3	chr9:1938085-1939097	GM12878	blood:	n/a	n/a
18	BCL3	chr9:1929851-1930230	GM12878	blood:	n/a	n/a
19	BCL3	chr9:1929602-1930726	GM12878	blood:	n/a	n/a
20	BCLAF1	chr9:1938023-1939269	GM12878	blood:	n/a	n/a
21	BCLAF1	chr9:1939341-1940537	GM12878	blood:	n/a	chr9:1940452-1940461
22	BCLAF1	chr9:1938005-1939350	GM12878	blood:	n/a	n/a
23	BCLAF1	chr9:1929618-1930478	GM12878	blood:	n/a	n/a
24	BCLAF1	chr9:1929681-1930911	GM12878	blood:	n/a	n/a
25	BHLHE40	chr9:1979943-1980099	GM12878	blood:	n/a	n/a
26	BHLHE40	chr9:1930434-1930697	K562	blood:	n/a	n/a
27	BHLHE40	chr9:1929603-1930840	GM12878	blood:	n/a	n/a
28	BHLHE40	chr9:1940045-1940494	GM12878	blood:	n/a	n/a
29	BHLHE40	chr9:1938164-1939182	GM12878	blood:	n/a	n/a
30	BRCA1	chr9:1938148-1938308	GM12878	blood:	n/a	n/a
31	BRCA1	chr9:1938573-1938623	GM12878	blood:	n/a	n/a
32	CEBPB	chr9:1978946-1979184	Hela-S3	cervix:	n/a	n/a
33	CEBPB	chr9:1986447-1986647	HepG2	liver:	n/a	n/a
34	CEBPB	chr9:1979709-1980112	ECC-1	luminal epithelium:	n/a	chr9:1979887-1979898 chr9:1979886-1979899 chr9:1979886-1979899
35	CEBPB	chr9:1979705-1980265	IMR90	lung:	n/a	chr9:1979887-1979898 chr9:1979886-1979899 chr9:1979886-1979899
36	CEBPB	chr9:1979729-1980088	Hela-S3	cervix:	n/a	chr9:1979887-1979898 chr9:1979886-1979899 chr9:1979886-1979899
37	CEBPB	chr9:1978880-1979225	IMR90	lung:	n/a	n/a
38	CEBPB	chr9:1958706-1958998	HepG2	liver:	n/a	chr9:1958849-1958858 chr9:1958751-1958762 chr9:1958848-1958859
39	CEBPB	chr9:1938742-1939040	GM12878	blood:	n/a	chr9:1938810-1938822
40	CEBPB	chr9:1979697-1980087	ECC-1	luminal epithelium:	n/a	chr9:1979887-1979898 chr9:1979886-1979899 chr9:1979886-1979899
41	CEBPB	chr9:1938063-1939341	GM12878	blood:	n/a	chr9:1938810-1938822
42	CEBPB	chr9:1952822-1953017	HepG2	liver:	n/a	chr9:1952884-1952895
43	CEBPB	chr9:1978954-1979451	HepG2	liver:	n/a	n/a
44	CEBPB	chr9:1929790-1930866	GM12878	blood:	n/a	chr9:1930742-1930755
45	CEBPB	chr9:1947605-1947834	HepG2	liver:	n/a	n/a
46	CEBPB	chr9:1979803-1980065	K562	blood:	n/a	chr9:1979887-1979898 chr9:1979886-1979899 chr9:1979886-1979899
47	CEBPB	chr9:1979709-1980080	HepG2	liver:	n/a	chr9:1979887-1979898 chr9:1979886-1979899 chr9:1979886-1979899
48	CEBPB	chr9:1979774-1980046	A549	lung:	n/a	chr9:1979887-1979898 chr9:1979886-1979899 chr9:1979886-1979899
49	CHD1	chr9:1940221-1940335	H1-hESC	embryonic stem cell:	n/a	n/a
50	CHD1	chr9:1938128-1939281	GM12878	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:1979255-1979305	GM12892	blood:	n/a
2	chr9:1979255-1979305	HEK293	kidney:	embryo
3	chr9:1979255-1979305	ovcar-3	ovarian:	n/a
4	chr9:1979255-1979305	NH-A	brain:	n/a
5	chr9:1979255-1979305	SKMC	muscle:	n/a
6	chr9:1979255-1979305	HL-60	blood:	n/a
7	chr9:1979255-1979305	Hela-S3	cervix:	n/a
8	chr9:1979255-1979305	HIPEpiC	eye:	n/a
9	chr9:1979255-1979305	HPAEpiC	pulmonary alveolar:	n/a
10	chr9:1979255-1979305	HMEC	breast:	n/a
11	chr9:1979255-1979305	HRE	kidney:	n/a
12	chr9:1979255-1979305	HCPEpiC	choroid plexus:	n/a
13	chr9:1979255-1979305	NHBE	bronchial:	n/a
14	chr9:1979255-1979305	Jurkat	blood:	n/a
15	chr9:1979255-1979305	Hepatocyte	liver:	n/a
16	chr9:1979255-1979305	GM12891	blood:	n/a
17	chr9:1979255-1979305	HCM	heart:	n/a
18	chr9:1979255-1979305	HNPCEpiC	eye:	n/a
19	chr9:1979255-1979305	HepG2	liver:	n/a
20	chr9:1979255-1979305	PANC-1	pancreas:	n/a
21	chr9:1979255-1979305	AoSMC	blood vessel:	n/a
22	chr9:1979255-1979305	SK-N-SH	brain:	n/a
23	chr9:1979255-1979305	SK-N-SH_RA	brain:	n/a
24	chr9:1979255-1979305	PFSK-1	brain:	n/a
25	chr9:1979255-1979305	AG09309	skin:	n/a
26	chr9:1979255-1979305	GM12878	blood:	n/a
27	chr9:1979255-1979305	NB4	blood:	n/a
28	chr9:1979255-1979305	MCF10A-Er-Src	breast:	n/a
29	chr9:1979255-1979305	Caco-2	colon:	n/a
30	chr9:1979255-1979305	LNCaP	prostate:	n/a
31	chr9:1979255-1979305	HEEpiC	esophagus:	n/a
32	chr9:1979255-1979305	K562	blood:	n/a
33	chr9:1979255-1979305	AG09319	gingival:	n/a
34	chr9:1979255-1979305	GM06990	blood:	n/a
35	chr9:1979255-1979305	GM19239	blood:	n/a
36	chr9:1979255-1979305	CMK	blood:	n/a
37	chr9:1979255-1979305	HUVEC	blood vessel:	n/a
38	chr9:1979255-1979305	AG10803	skin:	n/a
39	chr9:1979255-1979305	HCT-116	colon:	n/a
40	chr9:1979255-1979305	H1-hESC	embryonic stem cell:	embryo
41	chr9:1979255-1979305	SAEC	small airway:	n/a
42	chr9:1979255-1979305	HAEpiC	amniotic membrane:	n/a
43	chr9:1979255-1979305	AG04449	skin:	fetal
44	chr9:1979255-1979305	IMR90	lung:	fetal
45	chr9:1979255-1979305	RPTEC	kidney:	n/a
46	chr9:1979255-1979305	ProgFib	skin:	n/a
47	chr9:1979255-1979305	A549	lung:	n/a
48	chr9:1979255-1979305	NT2-D1	testis:	n/a
49	chr9:1979255-1979305	NHDF-neo	bronchial:	n/a
50	chr9:1979255-1979305	SK-N-MC	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr9:1928679..1931491-chr9:2015139..2017174,2	K562	blood:
2	chr9:1981753..1984012-chr9:2012148..2014267,2	K562	blood:
3	chr9:1941734..1942417-chr9:2087486..2088282,2	MCF-7	breast:
4	chr9:1989591..1991606-chr9:2004303..2006836,2	MCF-7	breast:
5	chr22:39715375..39715923-chr9:1928519..1929019,2	HCT-116	colon:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SMARCA2-2	chr9:1929409-1929562	XLOC_007264
2	lnc-KIAA0020-9	chr9:1930484-1930573	NONHSAT129978
3	lnc-KIAA0020-9	chr9:1929260-1929331	NONHSAT129978
4	lnc-SMARCA2-1	chr9:1929260-1929331	NONHSAT129979
5	lnc-SMARCA2-1	chr9:1930115-1930258	NONHSAT129979
6	lnc-KIAA0020-8	chr9:1977784-1978547	NONHSAT129981
7	lnc-KIAA0020-9	chr9:1930113-1930463	NONHSAT129978

Variant related genes	Relation type
ENSG00000224092	TF binding region
ENSG00000224092	CpG island
ENSG00000080503	chromatin interactions
ENSG00000100316	chromatin interactions

Extended variants
information (count: 2915 )
Associated
traits (count: 103 )

Variant overlapped rSNPs/rCNVs (count:2915 , 50 per page) page: 1 2 3 4 5 6 7 ... 59

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4014071	chr9:1928694-1928695	Flanking Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs116971163	chr9:1928700-1928701	Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs533623379	chr9:1928705-1928706	Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs576757194	chr9:1928706-1928707	Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs553833455	chr9:1928711-1928712	Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs145487488	chr9:1928721-1928722	Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs572274701	chr9:1928750-1928751	Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs562381388	chr9:1928761-1928762	Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs186222750	chr9:1928771-1928772	Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs147662410	chr9:1928825-1928826	Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs140949649	chr9:1928831-1928832	Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs558851035	chr9:1928835-1928836	Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs375123304	chr9:1928861-1928862	Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs79136625	chr9:1928887-1928888	Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs113758125	chr9:1928888-1928889	Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs138093643	chr9:1928907-1928908	Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs543815231	chr9:1928920-1928921	Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs563704974	chr9:1928968-1928969	Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs369948844	chr9:1929009-1929010	Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs10757030	chr9:1929030-1929031	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs551673993	chr9:1929031-1929032	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs564883691	chr9:1929032-1929033	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs527489049	chr9:1929114-1929115	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs117844919	chr9:1929118-1929119	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs531559119	chr9:1929178-1929179	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs190947191	chr9:1929193-1929194	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs537218396	chr9:1929203-1929204	Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs202123586	chr9:1929204-1929205	Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs534864620	chr9:1929218-1929219	Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs535970957	chr9:1929237-1929238	Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs184235881	chr9:1929255-1929256	Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs149073609	chr9:1929301-1929302	Weak transcription Flanking Active TSS	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
33	rs538937051	chr9:1929340-1929341	Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs144775421	chr9:1929369-1929370	Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs187464142	chr9:1929374-1929375	Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs548426196	chr9:1929388-1929389	Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs561831145	chr9:1929395-1929396	Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs572509631	chr9:1929461-1929462	Weak transcription Flanking Active TSS	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
39	rs377093555	chr9:1929497-1929498	Weak transcription Flanking Active TSS	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
40	rs10811138	chr9:1929502-1929503	Weak transcription Flanking Active TSS	Chromatin interactive region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs555226683	chr9:1929518-1929519	Weak transcription Flanking Active TSS	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
42	rs192720063	chr9:1929523-1929524	Weak transcription Flanking Active TSS	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
43	rs543946916	chr9:1929548-1929549	Weak transcription Flanking Active TSS	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
44	rs182857621	chr9:1929549-1929550	Weak transcription Flanking Active TSS	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
45	rs187078549	chr9:1929576-1929577	Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs544932124	chr9:1929599-1929600	Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs191832280	chr9:1929600-1929601	Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs138713359	chr9:1929664-1929665	Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs556900558	chr9:1929718-1929719	Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs531615148	chr9:1929719-1929720	Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:103)

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
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:233 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:1928000-1931000	Flanking Active TSS	GM12878-XiMat	blood
2	chr9:1928800-1929200	Enhancers	iPS-18 Cell Line	embryonic stem cell
3	chr9:1929200-1930400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
4	chr9:1929800-1930800	Enhancers	Primary B cells from peripheral blood	blood
5	chr9:1930400-1930800	Enhancers	K562	blood
6	chr9:1930600-1930800	Enhancers	iPS-18 Cell Line	embryonic stem cell
7	chr9:1937600-1937800	Enhancers	GM12878-XiMat	blood
8	chr9:1937800-1940600	Flanking Active TSS	GM12878-XiMat	blood
9	chr9:1938600-1940200	Enhancers	Primary B cells from peripheral blood	blood
10	chr9:1939000-1939200	Enhancers	Fetal Intestine Large	intestine
11	chr9:1940400-1940600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
12	chr9:1940600-1941800	Weak transcription	GM12878-XiMat	blood
13	chr9:1940600-1951200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
14	chr9:1942000-1942200	Enhancers	GM12878-XiMat	blood
15	chr9:1945400-1945600	Enhancers	Fetal Intestine Small	intestine
16	chr9:1945800-1946200	Enhancers	Fetal Intestine Large	intestine
17	chr9:1945800-1946800	Weak transcription	Fetal Intestine Small	intestine
18	chr9:1945800-1946800	Weak transcription	Pancreatic Islets	Pancreatic Islet
19	chr9:1945800-1947200	Enhancers	Cortex derived primary cultured neurospheres	brain
20	chr9:1946000-1946200	Enhancers	Fetal Brain Female	brain
21	chr9:1946200-1946400	Enhancers	Brain Hippocampus Middle	brain
22	chr9:1946200-1947000	Weak transcription	Fetal Brain Female	brain
23	chr9:1946200-1947400	Weak transcription	Fetal Intestine Large	intestine
24	chr9:1946400-1946800	Flanking Active TSS	Brain Hippocampus Middle	brain
25	chr9:1946600-1946800	Active TSS	Brain Cingulate Gyrus	brain
26	chr9:1946600-1947400	Enhancers	Fetal Brain Male	brain
27	chr9:1946800-1947000	Flanking Active TSS	Brain Cingulate Gyrus	brain
28	chr9:1946800-1947400	Enhancers	Brain Hippocampus Middle	brain
29	chr9:1946800-1947400	Enhancers	Fetal Intestine Small	intestine
30	chr9:1946800-1947600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
31	chr9:1946800-1948200	Enhancers	Pancreatic Islets	Pancreatic Islet
32	chr9:1947000-1947400	Enhancers	Stomach Mucosa	stomach
33	chr9:1947000-1947800	Enhancers	Fetal Brain Female	brain
34	chr9:1947000-1948000	Enhancers	Brain Cingulate Gyrus	brain
35	chr9:1947200-1949800	Weak transcription	Cortex derived primary cultured neurospheres	brain
36	chr9:1947400-1948200	Enhancers	Fetal Intestine Large	intestine
37	chr9:1947800-1948000	Enhancers	H1 Cell Line	embryonic stem cell
38	chr9:1948000-1950400	Weak transcription	H1 Cell Line	embryonic stem cell
39	chr9:1948200-1948400	Enhancers	iPS-20b Cell Line	embryonic stem cell
40	chr9:1948200-1950600	Weak transcription	Pancreatic Islets	Pancreatic Islet
41	chr9:1948400-1949200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
42	chr9:1948600-1949000	Enhancers	HUES48 Cell Line	embryonic stem cell
43	chr9:1949000-1950400	Weak transcription	HUES48 Cell Line	embryonic stem cell
44	chr9:1949000-1951200	Enhancers	iPS-15b Cell Line	embryonic stem cell
45	chr9:1949200-1949400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
46	chr9:1949200-1949600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
47	chr9:1949200-1950000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr9:1949200-1950000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
49	chr9:1949200-1952200	Enhancers	iPS-20b Cell Line	embryonic stem cell
50	chr9:1949200-1952400	Enhancers	iPS-18 Cell Line	embryonic stem cell

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