Variant report

Variant	esv2752281
Chromosome Location	chr9:13284600-13405072
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	BACH1	chr9:13367921-13368142	H1-hESC	embryonic stem cell:	n/a	n/a
2	BHLHE40	chr9:13315456-13315474	K562	blood:	n/a	n/a
3	CEBPB	chr9:13399120-13399349	A549	lung:	n/a	n/a
4	CTCF	chr9:13291800-13291950	AG04450	lung:	n/a	n/a
5	CTCF	chr9:13350919-13350987	GM10248	blood:	n/a	n/a
6	CTCF	chr9:13351820-13351970	NHEK	skin:	n/a	n/a
7	CTCF	chr9:13291880-13292030	AG09319	gingival:	n/a	n/a
8	CTCF	chr9:13352723-13352864	GM12878	blood:	n/a	n/a
9	CTCF	chr9:13330740-13330890	HFF-Myc	foreskin:	n/a	n/a
10	CTCF	chr9:13291800-13291950	BJ	skin:	n/a	n/a
11	CTCF	chr9:13363541-13363625	LNCaP	prostate:	n/a	n/a
12	CTCF	chr9:13351908-13352086	Lung_OC	lung:	n/a	chr9:13351959-13351980 chr9:13351958-13351974 chr9:13351957-13351975
13	CTCF	chr9:13351765-13352063	H1-hESC	embryonic stem cell:	n/a	chr9:13351959-13351980 chr9:13351958-13351974 chr9:13351957-13351975
14	CTCF	chr9:13351900-13352050	BE2_C	brain:	n/a	chr9:13351959-13351980 chr9:13351958-13351974 chr9:13351957-13351975
15	CTCF	chr9:13291821-13291941	Hela-S3	cervix:	n/a	n/a
16	CTCF	chr9:13351629-13352417	A549	lung:	n/a	chr9:13351959-13351980 chr9:13351958-13351974 chr9:13351957-13351975
17	CTCF	chr9:13351940-13352090	AG10803	skin:	n/a	chr9:13351959-13351980 chr9:13351958-13351974 chr9:13351957-13351975
18	CTCF	chr9:13351845-13352096	Medullo	brain:	n/a	chr9:13351959-13351980 chr9:13351958-13351974 chr9:13351957-13351975
19	CTCF	chr9:13291872-13291885	MCF-7	breast:	n/a	n/a
20	CTCF	chr9:13291860-13292010	BE2_C	brain:	n/a	n/a
21	CTCF	chr9:13351760-13351910	HFF-Myc	foreskin:	n/a	n/a
22	CTCF	chr9:13351840-13351990	GM12864	blood:	n/a	chr9:13351959-13351980 chr9:13351958-13351974 chr9:13351957-13351975
23	CTCF	chr9:13351839-13352102	HUVEC	blood vessel:	n/a	chr9:13351959-13351980 chr9:13351958-13351974 chr9:13351957-13351975
24	CTCF	chr9:13351860-13352010	HMEC	breast:	n/a	chr9:13351959-13351980 chr9:13351958-13351974 chr9:13351957-13351975
25	CTCF	chr9:13291900-13292050	HFF-Myc	foreskin:	n/a	n/a
26	CTCF	chr9:13323020-13323170	HVMF	connective:	n/a	n/a
27	CTCF	chr9:13351880-13352030	GM12870	blood:	n/a	chr9:13351959-13351980 chr9:13351958-13351974 chr9:13351957-13351975
28	CTCF	chr9:13351900-13352050	HMEC	breast:	n/a	chr9:13351959-13351980 chr9:13351958-13351974 chr9:13351957-13351975
29	CTCF	chr9:13329454-13329538	GM19238	blood:	n/a	n/a
30	CTCF	chr9:13291760-13291910	HA-sp	spinal cord:	n/a	n/a
31	CTCF	chr9:13351868-13352032	SK-N-SH_RA	brain:	n/a	chr9:13351959-13351980 chr9:13351958-13351974 chr9:13351957-13351975
32	CTCF	chr9:13291780-13291930	NHDF-neo	bronchial:	n/a	n/a
33	CTCF	chr9:13351880-13352030	NHDF-neo	bronchial:	n/a	chr9:13351959-13351980 chr9:13351958-13351974 chr9:13351957-13351975
34	CTCF	chr9:13351860-13352010	GM06990	blood:	n/a	chr9:13351959-13351980 chr9:13351958-13351974 chr9:13351957-13351975
35	CTCF	chr9:13351820-13351970	HFF	foreskin:	n/a	n/a
36	CTCF	chr9:13291720-13291870	AG04450	lung:	n/a	n/a
37	CTCF	chr9:13351880-13352030	GM12872	blood:	n/a	chr9:13351959-13351980 chr9:13351958-13351974 chr9:13351957-13351975
38	CTCF	chr9:13291820-13291970	HBMEC	blood vessel:	n/a	n/a
39	CTCF	chr9:13291800-13291950	HRPEpiC	eye:	n/a	n/a
40	CTCF	chr9:13351860-13352069	K562	blood:	n/a	chr9:13351959-13351980 chr9:13351958-13351974 chr9:13351957-13351975
41	CTCF	chr9:13351900-13352051	HepG2	liver:	n/a	chr9:13351959-13351980 chr9:13351958-13351974 chr9:13351957-13351975
42	CTCF	chr9:13351880-13352030	AoAF	blood vessel:	n/a	chr9:13351959-13351980 chr9:13351958-13351974 chr9:13351957-13351975
43	CTCF	chr9:13351420-13351570	NHEK	skin:	n/a	n/a
44	CTCF	chr9:13351920-13352070	HPAF	blood vessel:	n/a	chr9:13351959-13351980 chr9:13351958-13351974 chr9:13351957-13351975
45	CTCF	chr9:13291760-13291910	HCPEpiC	choroid plexus:	n/a	n/a
46	CTCF	chr9:13351920-13352070	GM12867	blood:	n/a	chr9:13351959-13351980 chr9:13351958-13351974 chr9:13351957-13351975
47	CTCF	chr9:13351900-13352050	HCPEpiC	choroid plexus:	n/a	chr9:13351959-13351980 chr9:13351958-13351974 chr9:13351957-13351975
48	CTCF	chr9:13351840-13351990	AG04450	lung:	n/a	chr9:13351959-13351980 chr9:13351958-13351974 chr9:13351957-13351975
49	CTCF	chr9:13351840-13351990	HA-sp	spinal cord:	n/a	chr9:13351959-13351980 chr9:13351958-13351974 chr9:13351957-13351975
50	CTCF	chr9:13351960-13352110	NHEK	skin:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:13323113-13323163	HAEpiC	amniotic membrane:	n/a
2	chr9:13323130-13323180	GM12878	blood:	n/a
3	chr9:13323130-13323180	ovcar-3	ovarian:	n/a
4	chr9:13323113-13323163	HCF	heart:	n/a
5	chr9:13284899-13284949	HCM	heart:	n/a
6	chr9:13284899-13284949	A549	lung:	n/a
7	chr9:13323113-13323163	Hepatocyte	liver:	n/a
8	chr9:13284899-13284949	Caco-2	colon:	n/a
9	chr9:13284899-13284949	GM19239	blood:	n/a
10	chr9:13323130-13323180	HEK293	kidney:	embryo
11	chr9:13323130-13323180	HCM	heart:	n/a
12	chr9:13323130-13323180	AG10803	skin:	n/a
13	chr9:13323113-13323163	BJ	skin:	n/a
14	chr9:13284899-13284949	BE2_C	brain:	n/a
15	chr9:13323113-13323163	HEK293	kidney:	embryo
16	chr9:13323130-13323180	PrEC	prostate:	n/a
17	chr9:13323130-13323180	GM06990	blood:	n/a
18	chr9:13323113-13323163	HIPEpiC	eye:	n/a
19	chr9:13323130-13323180	MCF10A-Er-Src	breast:	n/a
20	chr9:13323113-13323163	HPAEpiC	pulmonary alveolar:	n/a
21	chr9:13284899-13284949	RPTEC	kidney:	n/a
22	chr9:13323130-13323180	BJ	skin:	n/a
23	chr9:13323113-13323163	NB4	blood:	n/a
24	chr9:13323130-13323180	GM12892	blood:	n/a
25	chr9:13284899-13284949	HMEC	breast:	n/a
26	chr9:13284899-13284949	NH-A	brain:	n/a
27	chr9:13284899-13284949	SKMC	muscle:	n/a
28	chr9:13323113-13323163	Hela-S3	cervix:	n/a
29	chr9:13323130-13323180	PFSK-1	brain:	n/a
30	chr9:13323113-13323163	Caco-2	colon:	n/a
31	chr9:13323130-13323180	CMK	blood:	n/a
32	chr9:13323130-13323180	NT2-D1	testis:	n/a
33	chr9:13284899-13284949	MCF-7	breast:	n/a
34	chr9:13323113-13323163	HUVEC	blood vessel:	n/a
35	chr9:13284899-13284949	HEK293	kidney:	embryo
36	chr9:13323130-13323180	NH-A	brain:	n/a
37	chr9:13284899-13284949	HRCEpiC	kidney:	n/a
38	chr9:13323130-13323180	Caco-2	colon:	n/a
39	chr9:13284899-13284949	H1-hESC	embryonic stem cell:	embryo
40	chr9:13323113-13323163	SK-N-SH_RA	brain:	n/a
41	chr9:13284899-13284949	HL-60	blood:	n/a
42	chr9:13284899-13284949	HCT-116	colon:	n/a
43	chr9:13323113-13323163	HCT-116	colon:	n/a
44	chr9:13284899-13284949	AG09319	gingival:	n/a
45	chr9:13284899-13284949	AoSMC	blood vessel:	n/a
46	chr9:13323113-13323163	NT2-D1	testis:	n/a
47	chr9:13323113-13323163	HRE	kidney:	n/a
48	chr9:13323130-13323180	HAEpiC	amniotic membrane:	n/a
49	chr9:13284899-13284949	ECC-1	luminal epithelium:	n/a
50	chr9:13323130-13323180	Hepatocyte	liver:	n/a

No.	Distal block	Cell Line	Cell type
1	chr9:13403728..13406605-chr9:13406757..13409825,3	K562	blood:
2	chr9:13370327..13372389-chr9:13372731..13374721,2	MCF-7	breast:
3	chr9:13287399..13289604-chr9:13290158..13292995,2	K562	blood:
4	chr8:112133641..112134299-chr9:13359583..13360482,2	MCF-7	breast:
5	chr9:13394864..13396918-chr9:13399082..13401367,2	K562	blood:
6	chr9:13287399..13289604-chr9:13290158..13292995,2	K562	blood:
7	chr9:13351470..13352357-chr9:13423813..13424815,3	MCF-7	breast:
8	chr9:13281407..13283656-chr9:13286644..13288961,2	MCF-7	breast:
9	chr9:13370327..13372389-chr9:13372731..13374721,2	MCF-7	breast:
10	chr9:13351598..13352233-chr9:14353302..14354081,2	MCF-7	breast:
11	chr9:13276562..13283255-chr9:13284283..13286656,6	MCF-7	breast:
12	chr9:13394864..13396918-chr9:13399082..13401367,2	K562	blood:
13	chr9:13277467..13280147-chr9:13286399..13289258,3	MCF-7	breast:
14	chr9:13278476..13280409-chr9:13296744..13299210,3	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MPDZ-3	chr9:13322805-13323449	NONHSAT130234

Variant related genes	Relation type
ENSG00000223672	TF binding region
ENSG00000223672	CpG island
ENSG00000107186	chromatin interactions
ENSG00000234740	chromatin interactions

Extended variants
information (count: 3456 )
Associated
traits (count: 101 )

Variant overlapped rSNPs/rCNVs (count:3456 , 50 per page) page: 1 2 3 4 5 6 7 ... 70

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1023192	chr9:13284600-13284601	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs554419082	chr9:13284628-13284629	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs552963699	chr9:13284678-13284679	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs537353142	chr9:13284737-13284738	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs371384166	chr9:13284859-13284860	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs74913804	chr9:13284861-13284862	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs374669872	chr9:13284862-13284863	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs574127550	chr9:13284889-13284890	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs553181460	chr9:13284908-13284909	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs539806918	chr9:13284929-13284930	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs368056119	chr9:13284988-13284989	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs572606978	chr9:13285013-13285014	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs77964517	chr9:13285039-13285040	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs139745937	chr9:13285057-13285058	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs577913278	chr9:13285060-13285061	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs544106166	chr9:13285086-13285087	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs376989867	chr9:13285098-13285099	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs563794632	chr9:13285120-13285121	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs144555447	chr9:13285128-13285129	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs187336987	chr9:13285132-13285133	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs151033300	chr9:13285136-13285137	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs528214853	chr9:13285144-13285145	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs551059982	chr9:13285165-13285166	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs369961813	chr9:13285170-13285171	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs571229795	chr9:13285247-13285248	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs530389055	chr9:13285259-13285260	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs140940632	chr9:13285273-13285274	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs191390085	chr9:13285286-13285287	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs10961006	chr9:13285291-13285292	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs183786002	chr9:13285313-13285314	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs76873206	chr9:13285326-13285327	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs565514863	chr9:13285346-13285347	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs535125320	chr9:13285360-13285361	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs190277482	chr9:13285392-13285393	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs193269966	chr9:13285426-13285427	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs370813664	chr9:13285429-13285430	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs73647123	chr9:13285433-13285434	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs149785911	chr9:13285500-13285501	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs557305078	chr9:13285519-13285520	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs561551909	chr9:13285523-13285524	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs574032141	chr9:13285562-13285563	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs73647124	chr9:13285564-13285565	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs559568476	chr9:13285625-13285626	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs201482536	chr9:13285631-13285632	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs376596955	chr9:13285657-13285658	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs544716954	chr9:13285683-13285684	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs185696899	chr9:13285714-13285715	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs545930267	chr9:13285729-13285730	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs369559978	chr9:13285776-13285777	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs546989430	chr9:13285793-13285794	Weak transcription	Chromatin interactive region	2 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	22522925	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD
Breast cancer	21611746	CNVD

Chromatin state (count:313 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:13280200-13285200	Weak transcription	Ovary	ovary
2	chr9:13280200-13295600	Weak transcription	Aorta	Aorta
3	chr9:13281200-13285400	Enhancers	Fetal Heart	heart
4	chr9:13281800-13284600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
5	chr9:13282400-13284600	Enhancers	Breast Myoepithelial Primary Cells	Breast
6	chr9:13283000-13285400	Enhancers	Fetal Stomach	stomach
7	chr9:13283200-13284600	Enhancers	Fetal Lung	lung
8	chr9:13283600-13285400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
9	chr9:13284000-13284600	Enhancers	Fetal Kidney	kidney
10	chr9:13284000-13284600	Enhancers	NHLF	lung
11	chr9:13284600-13286800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
12	chr9:13286800-13287200	Enhancers	Breast Myoepithelial Primary Cells	Breast
13	chr9:13292400-13293200	Enhancers	Left Ventricle	heart
14	chr9:13292400-13293800	Enhancers	Fetal Heart	heart
15	chr9:13293800-13296200	Weak transcription	Fetal Heart	heart
16	chr9:13295600-13295800	Enhancers	Aorta	Aorta
17	chr9:13295600-13296000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
18	chr9:13315000-13315400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr9:13318000-13318400	Active TSS	Fetal Heart	heart
20	chr9:13320600-13321600	Enhancers	Adipose Nuclei	Adipose
21	chr9:13320800-13321600	Enhancers	Left Ventricle	heart
22	chr9:13321600-13324800	Weak transcription	Adipose Nuclei	Adipose
23	chr9:13321600-13330600	Weak transcription	Left Ventricle	heart
24	chr9:13322600-13323600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
25	chr9:13322800-13323000	Active TSS	Breast Myoepithelial Primary Cells	Breast
26	chr9:13322800-13324200	Enhancers	Colon Smooth Muscle	Colon
27	chr9:13323000-13323400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
28	chr9:13323000-13323400	Enhancers	Placenta	Placenta
29	chr9:13323000-13323400	Enhancers	Rectal Smooth Muscle	rectum
30	chr9:13323000-13323600	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
31	chr9:13323000-13323600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
32	chr9:13323000-13323600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
33	chr9:13323000-13323600	Active TSS	Stomach Smooth Muscle	stomach
34	chr9:13323000-13323600	Enhancers	NHEK	skin
35	chr9:13323400-13323800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
36	chr9:13323600-13324800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
37	chr9:13323600-13324800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
38	chr9:13323600-13325400	Enhancers	Breast Myoepithelial Primary Cells	Breast
39	chr9:13324800-13325200	Enhancers	Brain Cingulate Gyrus	brain
40	chr9:13324800-13325600	Enhancers	Adipose Nuclei	Adipose
41	chr9:13325000-13325200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
42	chr9:13325000-13325200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
43	chr9:13325000-13325400	Enhancers	NHDF-Ad	bronchial
44	chr9:13325000-13325600	Enhancers	HUVEC	blood vessel
45	chr9:13325400-13330200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
46	chr9:13325600-13327400	Weak transcription	Adipose Nuclei	Adipose
47	chr9:13325600-13330400	Weak transcription	HUVEC	blood vessel
48	chr9:13327400-13328400	Enhancers	Adipose Nuclei	Adipose
49	chr9:13328000-13328400	Enhancers	Fetal Heart	heart
50	chr9:13328400-13329600	Weak transcription	Adipose Nuclei	Adipose

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