Variant report

Variant	nsv613759
Chromosome Location	chr9:21455814-21492506
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	chr9:21461370-21461829	HepG2	liver:	n/a	n/a
2	CBX3	chr9:21465829-21466378	HCT-116	colon:	n/a	n/a
3	CEBPB	chr9:21478670-21478870	A549	lung:	n/a	chr9:21478675-21478688
4	CEBPB	chr9:21461343-21461732	HepG2	liver:	n/a	chr9:21461511-21461522
5	CTCF	chr9:21473120-21473270	HAc	cerebellar:	n/a	n/a
6	CTCF	chr9:21466080-21466230	GM12864	blood:	n/a	chr9:21466105-21466123 chr9:21466107-21466128 chr9:21466106-21466122 chr9:21466108-21466121
7	CTCF	chr9:21466060-21466210	MCF-7	breast:	n/a	chr9:21466105-21466123 chr9:21466107-21466128 chr9:21466106-21466122 chr9:21466108-21466121
8	CTCF	chr9:21491900-21492050	AG04449	skin:	n/a	chr9:21491933-21491954
9	CTCF	chr9:21466020-21466170	HA-sp	spinal cord:	n/a	chr9:21466105-21466123 chr9:21466107-21466128 chr9:21466106-21466122 chr9:21466108-21466121
10	CTCF	chr9:21492000-21492150	NHLF	lung:	n/a	n/a
11	CTCF	chr9:21466040-21466190	WERI-Rb-1	eye:	n/a	chr9:21466105-21466123 chr9:21466107-21466128 chr9:21466106-21466122 chr9:21466108-21466121
12	CTCF	chr9:21491860-21492010	NHDF-neo	bronchial:	n/a	chr9:21491933-21491954
13	CTCF	chr9:21466000-21466150	NHEK	skin:	n/a	chr9:21466105-21466123 chr9:21466107-21466128 chr9:21466106-21466122 chr9:21466108-21466121
14	CTCF	chr9:21465980-21466130	GM12878	blood:	n/a	chr9:21466105-21466123 chr9:21466107-21466128 chr9:21466106-21466122 chr9:21466108-21466121
15	CTCF	chr9:21473280-21473430	RPTEC	kidney:	n/a	chr9:21473366-21473387
16	CTCF	chr9:21465997-21466244	Medullo	brain:	n/a	chr9:21466105-21466123 chr9:21466107-21466128 chr9:21466106-21466122 chr9:21466108-21466121
17	CTCF	chr9:21466100-21466250	HEK293	kidney:	n/a	chr9:21466105-21466123 chr9:21466107-21466128 chr9:21466106-21466122 chr9:21466108-21466121
18	CTCF	chr9:21465981-21466235	LNCaP	prostate:	n/a	chr9:21466105-21466123 chr9:21466107-21466128 chr9:21466106-21466122 chr9:21466108-21466121
19	CTCF	chr9:21473420-21473570	GM12868	blood:	n/a	n/a
20	CTCF	chr9:21473280-21473430	AG04450	lung:	n/a	chr9:21473366-21473387
21	CTCF	chr9:21473260-21473410	RPTEC	kidney:	n/a	chr9:21473366-21473387
22	CTCF	chr9:21491833-21492031	LNCaP	prostate:	n/a	chr9:21491933-21491954
23	CTCF	chr9:21465917-21465998	GM12891	blood:	n/a	n/a
24	CTCF	chr9:21465961-21466252	Spleen_OC	spleen:	n/a	chr9:21466105-21466123 chr9:21466107-21466128 chr9:21466106-21466122 chr9:21466108-21466121
25	CTCF	chr9:21473200-21473350	GM12872	blood:	n/a	n/a
26	CTCF	chr9:21465956-21465972	Fibrobl	skin:	n/a	n/a
27	CTCF	chr9:21473300-21473450	HEEpiC	esophagus:	n/a	chr9:21473366-21473387
28	CTCF	chr9:21473340-21473490	GM12871	blood:	n/a	chr9:21473366-21473387
29	CTCF	chr9:21466022-21466169	T-47D	breast:	n/a	chr9:21466105-21466123 chr9:21466107-21466128 chr9:21466106-21466122 chr9:21466108-21466121
30	CTCF	chr9:21466040-21466190	AG10803	skin:	n/a	chr9:21466105-21466123 chr9:21466107-21466128 chr9:21466106-21466122 chr9:21466108-21466121
31	CTCF	chr9:21466060-21466210	HMF	breast:	n/a	chr9:21466105-21466123 chr9:21466107-21466128 chr9:21466106-21466122 chr9:21466108-21466121
32	CTCF	chr9:21473380-21473530	GM12872	blood:	n/a	n/a
33	CTCF	chr9:21465940-21466264	ECC-1	luminal epithelium:	n/a	chr9:21466105-21466123 chr9:21466107-21466128 chr9:21466106-21466122 chr9:21466108-21466121
34	CTCF	chr9:21466000-21466150	HFF-Myc	foreskin:	n/a	chr9:21466105-21466123 chr9:21466107-21466128 chr9:21466106-21466122 chr9:21466108-21466121
35	CTCF	chr9:21491803-21492065	T-47D	breast:	n/a	chr9:21491933-21491954
36	CTCF	chr9:21491765-21492122	MCF-7	breast:	n/a	chr9:21491933-21491954
37	CTCF	chr9:21473320-21473470	GM12873	blood:	n/a	chr9:21473366-21473387
38	CTCF	chr9:21479250-21479462	H1-hESC	embryonic stem cell:	n/a	n/a
39	CTCF	chr9:21466000-21466150	GM12866	blood:	n/a	chr9:21466105-21466123 chr9:21466107-21466128 chr9:21466106-21466122 chr9:21466108-21466121
40	CTCF	chr9:21473300-21473450	GM06990	blood:	n/a	chr9:21473366-21473387
41	CTCF	chr9:21491900-21492050	HFF-Myc	foreskin:	n/a	chr9:21491933-21491954
42	CTCF	chr9:21465745-21465842	GM19240	blood:	n/a	n/a
43	CTCF	chr9:21473320-21473470	A549	lung:	n/a	chr9:21473366-21473387
44	CTCF	chr9:21491860-21492010	BJ	skin:	n/a	chr9:21491933-21491954
45	CTCF	chr9:21491960-21492110	RPTEC	kidney:	n/a	n/a
46	CTCF	chr9:21491840-21491990	AG10803	skin:	n/a	chr9:21491933-21491954
47	CTCF	chr9:21466020-21466170	GM12872	blood:	n/a	chr9:21466105-21466123 chr9:21466107-21466128 chr9:21466106-21466122 chr9:21466108-21466121
48	CTCF	chr9:21466016-21466204	GM20000	blood:	n/a	chr9:21466105-21466123 chr9:21466107-21466128 chr9:21466106-21466122 chr9:21466108-21466121
49	CTCF	chr9:21473320-21473470	AG04450	lung:	n/a	chr9:21473366-21473387
50	CTCF	chr9:21465340-21465490	GM12875	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr9:21491433..21492444-chr9:21789127..21790263,7	MCF-7	breast:
2	chr9:21464451..21467378-chr9:21800569..21802345,2	MCF-7	breast:
3	chr9:21465480..21466871-chr9:21788898..21790282,6	MCF-7	breast:
4	chr9:21465639..21466595-chr9:21789434..21790168,4	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-IFNE-1	chr9:21454267-21455943	NONHSAT130386
2	lnc-IFNE-1	chr9:21476898-21477034	NONHSAT130388
3	lnc-IFNE-1	chr9:21476898-21477034	NONHSAT130385
4	lnc-IFNE-1	chr9:21455587-21455943	NONHSAT130388
5	lnc-IFNE-1	chr9:21454267-21455943	NONHSAT130385
6	lnc-IFNE-1	chr9:21476898-21477034	ENSG00000171889
7	lnc-IFNE-1	chr9:21477168-21477291	ENSG00000171889
8	lnc-IFNA1-1	chr9:21455483-21456048	NONHSAT130387
9	lnc-IFNE-1	chr9:21476898-21477034	NONHSAT130386
10	lnc-IFNE-1	chr9:21477168-21477291	NONHSAT130386
11	lnc-IFNE-1	chr9:21477168-21477291	NONHSAT130385
12	lnc-IFNE-1	chr9:21477168-21477292	NONHSAT130389
13	lnc-IFNE-1	chr9:21477168-21477292	NONHSAT130388
14	lnc-IFNE-1	chr9:21455641-21455943	ENSG00000171889
15	lnc-IFNE-1	chr9:21476873-21477034	NONHSAT130389

Variant related genes	Relation type
IFNE	TF binding region
RPP40	miRNA target sites
RAB14	miRNA target sites
EEF1A1	miRNA target sites

Extended variants
information (count: 1566 )
Associated
traits (count: 158 )

Variant overlapped rSNPs/rCNVs (count:1566 , 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	rs10965002	chr9:21455814-21455815	Weak transcription Strong transcription Genic enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs116295480	chr9:21455815-21455816	Weak transcription Strong transcription Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
3	rs539883894	chr9:21455831-21455832	Weak transcription Strong transcription Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
4	rs560161707	chr9:21455845-21455846	Weak transcription Strong transcription Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
5	rs534359317	chr9:21455853-21455854	Weak transcription Strong transcription Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
6	rs199680563	chr9:21455869-21455870	Weak transcription Strong transcription Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
7	rs569744130	chr9:21455914-21455915	Weak transcription Strong transcription Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
8	rs532215822	chr9:21455915-21455916	Weak transcription Strong transcription Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
9	rs531830407	chr9:21455975-21455976	Weak transcription Strong transcription Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
10	rs147801927	chr9:21456003-21456004	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
11	rs565473230	chr9:21456015-21456016	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
12	rs189956801	chr9:21456060-21456061	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs141289848	chr9:21456120-21456121	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs56106002	chr9:21456204-21456205	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs535760725	chr9:21456216-21456217	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs146984170	chr9:21456234-21456235	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs113010660	chr9:21456237-21456238	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs536751267	chr9:21456242-21456243	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs550336361	chr9:21456245-21456246	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs183803620	chr9:21456247-21456248	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs538069418	chr9:21456248-21456249	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs189116196	chr9:21456254-21456255	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs371348519	chr9:21456256-21456257	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs577878526	chr9:21456288-21456289	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs568595166	chr9:21456303-21456304	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs533754206	chr9:21456314-21456315	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs148059181	chr9:21456366-21456367	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs191466944	chr9:21456374-21456375	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs556799013	chr9:21456394-21456395	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs112012137	chr9:21456491-21456492	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs183684387	chr9:21456492-21456493	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs562269689	chr9:21456513-21456514	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs187809788	chr9:21456619-21456620	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs150188495	chr9:21456641-21456642	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs565545084	chr9:21456661-21456662	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs115498944	chr9:21456677-21456678	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs575100202	chr9:21456678-21456679	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs191634531	chr9:21456691-21456692	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs138735455	chr9:21456697-21456698	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs530161616	chr9:21456699-21456700	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs539246767	chr9:21456721-21456722	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs116700521	chr9:21456752-21456753	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs184146506	chr9:21456763-21456764	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs111633772	chr9:21456768-21456769	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs573272990	chr9:21456772-21456773	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs10491569	chr9:21456776-21456777	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
47	rs534394252	chr9:21456797-21456798	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs571472361	chr9:21456799-21456800	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs368341777	chr9:21456800-21456801	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs533855971	chr9:21456829-21456830	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:158)

Disease	PMID	Source
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	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
Oral squamous cell carcinoma	17134496	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
Chronic lymphocytic leukemia	21546498	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
microdeletion syndrome	16199537	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Cancer	20164919	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
Chronic myeloid leukemia	21384125	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
Metanephric adenoma	20802469	CNVD
Developmental delay	21147756	CNVD
Pilocytic astrocytoma	18670637	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Melanoma	22183965	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Non-small cell lung cancer	19010865	CNVD
Myoepithelioma	18604193	CNVD
Cancer	22183965	CNVD
Glioblastoma multiforme	21569311	CNVD
Myelofibrosis	22110671	CNVD
Ewing''s sarcoma	22429812	CNVD
Neuroblastoma	21899760	CNVD
Glioblastoma multiforme	19435819	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Glioblastoma multiforme	22291905	CNVD
Lung cancer	21911935	CNVD
Primary central nervous system lymphoma	21088137	CNVD
head and neck squamous cell carcinoma	21798897	CNVD
Cancer	21253487	CNVD
Glioblastoma multiforme	22286061	CNVD
Intracranial ependymoma	16609018	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Glioblastoma multiforme	21922591	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Urothelial cell carcinoma	18451213	CNVD
Glioma	17123091	CNVD
Mental retardation	17124404	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Acute lymphoblastic leukemia	18768390	CNVD
Leukemia	19602459	CNVD
Acute monocytic leukemia	16498392	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Leukemia	18688285	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Acute myeloid leukemia	19651601	CNVD
Coronary Disease	20032323	CNVD
Squamous cell cancer	20885788	CNVD
Hirschsprung''s Disease	21712996	CNVD
Cancer	21732550	CNVD
Gastric cancer	22539939	CNVD
Cancer	21183584	CNVD
T-cell lymphomas	19863542	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Metastatic melanoma	18483359	CNVD
Non-small cell lung cancer	20864512	CNVD
Cervical cancer	21062161	CNVD
Acute myeloid leukemia	16864856	CNVD
Glioblastoma	17090523	CNVD
Lung cancer	16773561	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Colorectal cancer	16774939	CNVD
Bladder cancer	19088036	CNVD
Colorectal cancer	16272173	CNVD
Melanoma	16977458	CNVD
Glioblastoma multiforme	17369134	CNVD
Chagasic megaesophagus	20163722	CNVD
Melanoma	19566914	CNVD
Squamous cell cancer	19047905	CNVD
Lung adenocarcinoma	19525976	CNVD
Lung cancer	19525976	CNVD
Hodgkin''s lymphoma	18179710	CNVD
Glioma	20126413	CNVD
Melanoma	17363583	CNVD
Glioblastoma multiforme	19115005	CNVD
Glioblastoma multiforme	21525872	CNVD
Glioblastoma multiforme	21138945	CNVD
Adenoid cystic carcinoma	18332873	CNVD
Breast cancer	21364760	CNVD
Cancer	20581869	CNVD
Multiple myeloma	17550852	CNVD
Intellectual disability	22102821	CNVD
Oral cancer	22144094	CNVD
Lung cancer	21569311	CNVD
Epilepsy	20502679	CNVD
Barrett''s syndrome	19417022	CNVD
Pancreatic cancer	21811587	CNVD
Breast cancer	22522925	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD
Chronic lymphocytic leukemia	21215367	CNVD
Renal cell carcinoma	21215367	CNVD
Ovarian cancer	21781307	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Cancer	20164920	CNVD

Chromatin state (count:217 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:21451400-21458800	Weak transcription	A549	lung
2	chr9:21451800-21457600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
3	chr9:21453200-21456200	Strong transcription	NH-A	brain
4	chr9:21453800-21456000	Genic enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr9:21454400-21456200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
6	chr9:21454800-21474400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
7	chr9:21454800-21481600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr9:21455000-21456800	Weak transcription	Hela-S3	cervix
9	chr9:21455000-21457200	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
10	chr9:21455200-21456000	Genic enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
11	chr9:21455200-21456000	Genic enhancers	NHEK	skin
12	chr9:21455200-21457200	Strong transcription	Osteobl	bone
13	chr9:21455200-21464000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
14	chr9:21455200-21481000	Weak transcription	NHDF-Ad	bronchial
15	chr9:21455400-21456000	Strong transcription	HMEC	breast
16	chr9:21455400-21456400	Strong transcription	Muscle Satellite Cultured Cells	--
17	chr9:21455400-21462600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
18	chr9:21455600-21456000	Genic enhancers	NHLF	lung
19	chr9:21455800-21456000	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
20	chr9:21455800-21457000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
21	chr9:21455800-21481000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
22	chr9:21456000-21457200	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
23	chr9:21456000-21462800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
24	chr9:21456000-21463200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
25	chr9:21456000-21465000	Weak transcription	NHEK	skin
26	chr9:21456000-21465400	Weak transcription	HMEC	breast
27	chr9:21456000-21476600	Weak transcription	NHLF	lung
28	chr9:21456200-21461400	Weak transcription	NH-A	brain
29	chr9:21456400-21462400	Weak transcription	Muscle Satellite Cultured Cells	--
30	chr9:21457000-21462000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
31	chr9:21457200-21460400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
32	chr9:21457200-21462600	Weak transcription	Osteobl	bone
33	chr9:21457200-21462800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
34	chr9:21460400-21461800	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
35	chr9:21461400-21466200	Strong transcription	NH-A	brain
36	chr9:21461800-21462600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
37	chr9:21462000-21466000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
38	chr9:21462200-21463000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
39	chr9:21462400-21464200	Weak transcription	HUVEC	blood vessel
40	chr9:21462400-21466000	Strong transcription	Muscle Satellite Cultured Cells	--
41	chr9:21462600-21466000	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
42	chr9:21462600-21466800	Strong transcription	Osteobl	bone
43	chr9:21462600-21474600	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
44	chr9:21462800-21463200	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
45	chr9:21462800-21463200	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
46	chr9:21463000-21463200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
47	chr9:21463000-21502200	Weak transcription	HSMM	muscle
48	chr9:21463200-21464800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
49	chr9:21463200-21465200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
50	chr9:21463200-21465800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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