Variant report

Variant	nsv892741
Chromosome Location	chr9:21517302-21551513
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	BCL3	chr9:21519608-21520690	A549	lung:	n/a	chr9:21519928-21519937
2	BCL3	chr9:21548899-21550745	A549	lung:	n/a	n/a
3	BCL3	chr9:21549187-21550089	A549	lung:	n/a	n/a
4	BRCA1	chr9:21548988-21549868	Hela-S3	cervix:	n/a	n/a
5	BRCA1	chr9:21548534-21548634	Hela-S3	cervix:	n/a	n/a
6	CBX3	chr9:21520811-21522028	HCT-116	colon:	n/a	n/a
7	CBX3	chr9:21519763-21526025	HCT-116	colon:	n/a	n/a
8	CBX3	chr9:21522147-21524471	HCT-116	colon:	n/a	n/a
9	CBX3	chr9:21526174-21527163	HCT-116	colon:	n/a	n/a
10	CEBPB	chr9:21519283-21525730	HCT-116	colon:	n/a	n/a
11	CEBPB	chr9:21519556-21521968	HCT-116	colon:	n/a	n/a
12	CEBPB	chr9:21549138-21550039	Hela-S3	cervix:	n/a	chr9:21549276-21549287 chr9:21549692-21549703
13	CEBPB	chr9:21549213-21550026	IMR90	lung:	n/a	chr9:21549276-21549287 chr9:21549692-21549703
14	CEBPB	chr9:21549459-21550071	A549	lung:	n/a	chr9:21549692-21549703
15	CEBPB	chr9:21549163-21550161	HCT-116	colon:	n/a	chr9:21549276-21549287 chr9:21549692-21549703
16	CEBPB	chr9:21551365-21551981	A549	lung:	n/a	n/a
17	CEBPB	chr9:21549112-21550105	A549	lung:	n/a	chr9:21549276-21549287 chr9:21549692-21549703
18	CEBPB	chr9:21549314-21550172	A549	lung:	n/a	chr9:21549692-21549703
19	CHD2	chr9:21549127-21549911	Hela-S3	cervix:	n/a	n/a
20	CREB1	chr9:21549320-21549833	A549	lung:	n/a	n/a
21	CREB1	chr9:21549503-21549856	A549	lung:	n/a	n/a
22	CTCF	chr9:21527820-21527970	HCPEpiC	choroid plexus:	n/a	n/a
23	CTCF	chr9:21549540-21549690	RPTEC	kidney:	n/a	n/a
24	CTCF	chr9:21527680-21527830	SAEC	small airway:	n/a	n/a
25	CTCF	chr9:21527703-21527955	GM12891	blood:	n/a	n/a
26	CTCF	chr9:21527840-21527990	HRPEpiC	eye:	n/a	n/a
27	CTCF	chr9:21527760-21527910	SAEC	small airway:	n/a	n/a
28	CTCF	chr9:21527700-21527850	GM06990	blood:	n/a	n/a
29	CTCF	chr9:21527780-21527930	Hela-S3	cervix:	n/a	n/a
30	CTCF	chr9:21527720-21527870	HRE	kidney:	n/a	n/a
31	CTCF	chr9:21527756-21527908	GM13977	blood:	n/a	n/a
32	CTCF	chr9:21527720-21527870	GM12872	blood:	n/a	n/a
33	CTCF	chr9:21527760-21527910	GM12875	blood:	n/a	n/a
34	CTCF	chr9:21527780-21527930	GM12878	blood:	n/a	n/a
35	CTCF	chr9:21527720-21527870	HMEC	breast:	n/a	n/a
36	CTCF	chr9:21527800-21527950	WERI-Rb-1	eye:	n/a	n/a
37	CTCF	chr9:21527760-21527910	HUVEC	blood vessel:	n/a	n/a
38	CTCF	chr9:21549635-21549662	Hela-S3	cervix:	n/a	n/a
39	CTCF	chr9:21527520-21527670	HUVEC	blood vessel:	n/a	n/a
40	CTCF	chr9:21527740-21527890	HFF	foreskin:	n/a	n/a
41	CTCF	chr9:21527700-21527850	GM12864	blood:	n/a	n/a
42	CTCF	chr9:21527746-21527914	Spleen_OC	spleen:	n/a	n/a
43	CTCF	chr9:21527920-21528070	AG04450	lung:	n/a	n/a
44	CTCF	chr9:21533140-21533290	HPF	lung:	n/a	n/a
45	CTCF	chr9:21527720-21527870	NHEK	skin:	n/a	n/a
46	CTCF	chr9:21527738-21527890	HepG2	liver:	n/a	n/a
47	CTCF	chr9:21527720-21527870	GM06990	blood:	n/a	n/a
48	CTCF	chr9:21527730-21527938	GM19239	blood:	n/a	n/a
49	CTCF	chr9:21527753-21527934	NHEK	skin:	n/a	n/a
50	CTCF	chr9:21527720-21527870	GM12873	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr14:68668658..68669180-chr9:21520044..21520625,2	HCT-116	colon:
2	chr14:74955326..74955958-chr9:21530738..21531280,2	HCT-116	colon:
3	chr11:61583818..61584553-chr9:21518322..21519322,2	HCT-116	colon:

Variant related genes	Relation type
ENSG00000264379	TF binding region
ENSG00000134824	chromatin interactions
ENSG00000149485	chromatin interactions

Extended variants
information (count: 1435 )
Associated
traits (count: 154 )

Variant overlapped rSNPs/rCNVs (count:1435 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10965044	chr9:21517302-21517303	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs574323184	chr9:21517329-21517330	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs542609980	chr9:21517370-21517371	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs562911738	chr9:21517396-21517397	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs187727270	chr9:21517401-21517402	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs367903667	chr9:21517415-21517416	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs149821591	chr9:21517466-21517467	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs565065451	chr9:21517487-21517488	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs10965045	chr9:21517492-21517493	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs79740364	chr9:21517513-21517514	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs191023009	chr9:21517530-21517531	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs183503607	chr9:21517535-21517536	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs538818051	chr9:21517581-21517582	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs529189785	chr9:21517585-21517586	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs375796999	chr9:21517618-21517619	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs548658265	chr9:21517619-21517620	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs374141014	chr9:21517649-21517650	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs148565723	chr9:21517657-21517658	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs187462041	chr9:21517669-21517670	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs577109311	chr9:21517675-21517676	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs537871864	chr9:21517683-21517684	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs192215786	chr9:21517734-21517735	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs551487721	chr9:21517760-21517761	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs376080861	chr9:21517762-21517763	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs77299672	chr9:21517813-21517814	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs113680236	chr9:21517814-21517815	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs374598693	chr9:21517815-21517816	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs571408842	chr9:21517882-21517883	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs534390615	chr9:21517887-21517888	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs554348166	chr9:21517894-21517895	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs199501911	chr9:21517922-21517923	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs548020345	chr9:21517923-21517924	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs184641638	chr9:21517924-21517925	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs76272239	chr9:21517932-21517933	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs556256189	chr9:21517977-21517978	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs188276031	chr9:21518005-21518006	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs571024468	chr9:21518031-21518032	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs192172651	chr9:21518059-21518060	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs578013719	chr9:21518063-21518064	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs558616332	chr9:21518071-21518072	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs569189696	chr9:21518077-21518078	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs184445594	chr9:21518141-21518142	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs144471223	chr9:21518180-21518181	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs545288084	chr9:21518200-21518201	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs560302248	chr9:21518214-21518215	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs529138847	chr9:21518232-21518233	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs146638743	chr9:21518233-21518234	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs562807384	chr9:21518260-21518261	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs10965046	chr9:21518275-21518276	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs572223070	chr9:21518327-21518328	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:154)

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
Oral cancer	22144094	CNVD
Lung cancer	21569311	CNVD
Epilepsy	20502679	CNVD
Barrett''s syndrome	19417022	CNVD
Breast cancer	22522925	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD
Cancer	20164920	CNVD
Non-small cell lung cancer	16651412	CNVD
Breast cancer	17142309	CNVD

Chromatin state (count:552 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:21466000-21527600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr9:21494800-21527600	Weak transcription	Gastric	stomach
3	chr9:21507200-21551400	Weak transcription	H9 Cell Line	embryonic stem cell
4	chr9:21507400-21527200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
5	chr9:21508000-21542000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
6	chr9:21508200-21523200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
7	chr9:21508200-21527600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
8	chr9:21508200-21527600	Weak transcription	Fetal Intestine Small	intestine
9	chr9:21508600-21517600	Weak transcription	Fetal Intestine Large	intestine
10	chr9:21510400-21527600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
11	chr9:21512200-21517600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
12	chr9:21512200-21517600	Weak transcription	NH-A	brain
13	chr9:21512200-21526400	Weak transcription	Duodenum Mucosa	Duodenum
14	chr9:21512200-21526600	Weak transcription	HSMM	muscle
15	chr9:21512800-21527000	Weak transcription	NHLF	lung
16	chr9:21513000-21526600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
17	chr9:21514400-21519000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
18	chr9:21514400-21527000	Weak transcription	Hela-S3	cervix
19	chr9:21514600-21517800	Enhancers	NHDF-Ad	bronchial
20	chr9:21514600-21519400	Weak transcription	HUVEC	blood vessel
21	chr9:21515000-21518400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr9:21515600-21519000	Strong transcription	Muscle Satellite Cultured Cells	--
23	chr9:21516000-21518600	Genic enhancers	A549	lung
24	chr9:21516200-21520200	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
25	chr9:21516600-21519000	Strong transcription	HMEC	breast
26	chr9:21516600-21519000	Strong transcription	Osteobl	bone
27	chr9:21516800-21517600	Genic enhancers	NHEK	skin
28	chr9:21516800-21517800	Genic enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
29	chr9:21516800-21542600	Weak transcription	Stomach Mucosa	stomach
30	chr9:21517000-21518400	Genic enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
31	chr9:21517600-21518200	Enhancers	Breast Myoepithelial Primary Cells	Breast
32	chr9:21517600-21518600	Strong transcription	NHEK	skin
33	chr9:21517600-21521600	Strong transcription	NH-A	brain
34	chr9:21517800-21518200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
35	chr9:21517800-21519800	Weak transcription	NHDF-Ad	bronchial
36	chr9:21518200-21520200	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
37	chr9:21518200-21526400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
38	chr9:21518400-21519400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
39	chr9:21518400-21520600	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
40	chr9:21518600-21519000	Genic enhancers	NHEK	skin
41	chr9:21518600-21519400	Strong transcription	A549	lung
42	chr9:21519000-21519200	Genic enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
43	chr9:21519000-21520000	Weak transcription	Osteobl	bone
44	chr9:21519000-21521400	Strong transcription	NHEK	skin
45	chr9:21519000-21524400	Weak transcription	HMEC	breast
46	chr9:21519000-21525800	Weak transcription	Muscle Satellite Cultured Cells	--
47	chr9:21519200-21519800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
48	chr9:21519400-21520200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
49	chr9:21519400-21520400	Genic enhancers	A549	lung
50	chr9:21519400-21520400	Enhancers	HUVEC	blood vessel

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