Variant report

Variant	nsv892764
Chromosome Location	chr9:22680915-22755025
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	CEBPB	chr9:22683693-22684086	IMR90	lung:	n/a	n/a
2	CEBPB	chr9:22696362-22696521	Hela-S3	cervix:	n/a	chr9:22696461-22696470 chr9:22696459-22696472 chr9:22696461-22696470 chr9:22696461-22696470 chr9:22696459-22696472
3	CEBPB	chr9:22709513-22709726	A549	lung:	n/a	n/a
4	CEBPB	chr9:22709428-22709726	IMR90	lung:	n/a	n/a
5	CEBPB	chr9:22709485-22709771	HepG2	liver:	n/a	n/a
6	CEBPB	chr9:22682459-22682654	Hela-S3	cervix:	n/a	n/a
7	CEBPB	chr9:22683155-22683272	A549	lung:	n/a	chr9:22683166-22683179
8	CEBPB	chr9:22683049-22683464	IMR90	lung:	n/a	chr9:22683166-22683179
9	CEBPB	chr9:22683718-22684087	Hela-S3	cervix:	n/a	n/a
10	CEBPB	chr9:22696377-22696528	H1-hESC	embryonic stem cell:	n/a	chr9:22696461-22696470 chr9:22696459-22696472 chr9:22696461-22696470 chr9:22696461-22696470 chr9:22696459-22696472
11	CEBPB	chr9:22683775-22683981	MCF-7	breast:	n/a	n/a
12	CEBPB	chr9:22696309-22696578	IMR90	lung:	n/a	chr9:22696461-22696470 chr9:22696459-22696472 chr9:22696461-22696470 chr9:22696461-22696470 chr9:22696459-22696472
13	CEBPB	chr9:22695388-22695662	IMR90	lung:	n/a	n/a
14	CEBPB	chr9:22693164-22693367	IMR90	lung:	n/a	n/a
15	CEBPB	chr9:22683053-22683457	Hela-S3	cervix:	n/a	chr9:22683166-22683179
16	CTCF	chr9:22718780-22718930	HRPEpiC	eye:	n/a	chr9:22718838-22718854 chr9:22718837-22718855
17	CTCF	chr9:22717280-22717430	HBMEC	blood vessel:	n/a	n/a
18	CTCF	chr9:22718689-22718987	GM12878	blood:	n/a	chr9:22718838-22718854 chr9:22718837-22718855
19	CTCF	chr9:22718660-22718810	RPTEC	kidney:	n/a	n/a
20	CTCF	chr9:22717340-22717490	HMEC	breast:	n/a	n/a
21	CTCF	chr9:22718760-22718910	HPF	lung:	n/a	chr9:22718838-22718854 chr9:22718837-22718855
22	CTCF	chr9:22718740-22718890	HPF	lung:	n/a	chr9:22718838-22718854 chr9:22718837-22718855
23	CTCF	chr9:22718740-22718890	AG09319	gingival:	n/a	chr9:22718838-22718854 chr9:22718837-22718855
24	CTCF	chr9:22719100-22719250	RPTEC	kidney:	n/a	n/a
25	CTCF	chr9:22718720-22718870	AG09319	gingival:	n/a	chr9:22718838-22718854 chr9:22718837-22718855
26	CTCF	chr9:22718760-22718910	HEK293	kidney:	n/a	chr9:22718838-22718854 chr9:22718837-22718855
27	CTCF	chr9:22718780-22718930	HCPEpiC	choroid plexus:	n/a	chr9:22718838-22718854 chr9:22718837-22718855
28	CTCF	chr9:22717363-22717368	LNCaP	prostate:	n/a	n/a
29	CTCF	chr9:22718700-22718850	HRE	kidney:	n/a	n/a
30	CTCF	chr9:22717341-22717424	MCF-7	breast:	n/a	n/a
31	CTCF	chr9:22718720-22718870	HRPEpiC	eye:	n/a	chr9:22718838-22718854 chr9:22718837-22718855
32	CTCF	chr9:22717220-22717370	HMEC	breast:	n/a	n/a
33	CTCF	chr9:22718740-22718890	AoAF	blood vessel:	n/a	chr9:22718838-22718854 chr9:22718837-22718855
34	CTCF	chr9:22717260-22717410	AoAF	blood vessel:	n/a	n/a
35	CTCF	chr9:22718780-22718930	HPAF	blood vessel:	n/a	chr9:22718838-22718854 chr9:22718837-22718855
36	CTCF	chr9:22718840-22718990	HCT-116	colon:	n/a	n/a
37	CTCF	chr9:22717240-22717390	MCF-7	breast:	n/a	n/a
38	CTCF	chr9:22718780-22718930	AoAF	blood vessel:	n/a	chr9:22718838-22718854 chr9:22718837-22718855
39	CTCF	chr9:22702521-22702563	GM20000	blood:	n/a	n/a
40	CTCF	chr9:22719120-22719270	AG10803	skin:	n/a	n/a
41	CTCF	chr9:22717180-22717330	HPF	lung:	n/a	n/a
42	CTCF	chr9:22718728-22718956	IMR90	lung:	n/a	chr9:22718838-22718854 chr9:22718837-22718855
43	CTCF	chr9:22718800-22718950	GM12872	blood:	n/a	chr9:22718838-22718854 chr9:22718837-22718855
44	CTCF	chr9:22719080-22719230	AG04450	lung:	n/a	n/a
45	CTCF	chr9:22717360-22717510	RPTEC	kidney:	n/a	n/a
46	CTCF	chr9:22681020-22681170	HFF	foreskin:	n/a	n/a
47	CTCF	chr9:22718120-22718270	NHLF	lung:	n/a	n/a
48	CTCF	chr9:22717300-22717450	HMF	breast:	n/a	n/a
49	CTCF	chr9:22717340-22717490	HRE	kidney:	n/a	n/a
50	CTCF	chr9:22718280-22718430	HMF	breast:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr15:65596780..65597412-chr9:22707344..22708364,4	MCF-7	breast:
2	chr15:65596803..65598452-chr9:22707864..22709364,2	K562	blood:
3	chr15:65596519..65598485-chr9:22707844..22709364,2	MCF-7	breast:
4	chr7:2109017..2109524-chr9:22685897..22686685,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DMRTA1-1	chr9:22682469-22683267	NONHSAT130441
2	lnc-DMRTA1-14	chr9:22754997-22755223	NONHSAT130447
3	lnc-DMRTA1-2	chr9:22723308-22723429	ENSG00000234840.1
4	lnc-DMRTA1-2	chr9:22687546-22687626	ENSG00000234840.1
5	lnc-DMRTA1-12	chr9:22728286-22728585	NONHSAT130446
6	lnc-DMRTA1-1	chr9:22682609-22682712	NONHSAT130443
7	lnc-DMRTA1-1	chr9:22683873-22684083	NONHSAT130441
8	lnc-DMRTA1-1	chr9:22723308-22723429	NONHSAT130443
9	lnc-DMRTA1-1	chr9:22687546-22688453	NONHSAT130441
10	lnc-DMRTA1-11	chr9:22716040-22716456	NONHSAT130445
11	lnc-DMRTA1-12	chr9:22725718-22725880	NONHSAT130446
12	lnc-DMRTA1-2	chr9:22682469-22682712	ENSG00000234840.1
13	lnc-DMRTA1-10	chr9:22713308-22713435	l_3742_chr9:22664441-22713435_adipose
14	lnc-DMRTA1-11	chr9:22714322-22715083	NONHSAT130445
15	lnc-DMRTA1-11	chr9:22715216-22715757	NONHSAT130445
16	lnc-DMRTA1-2	chr9:22682609-22682712	ENSG00000234840.1

Variant related genes	Relation type
ENSG00000236739	TF binding region
ENSG00000234840	TF binding region
ENSG00000200156	chromatin interactions

Extended variants
information (count: 2744 )
Associated
traits (count: 154 )

Variant overlapped rSNPs/rCNVs (count:2744 , 50 per page) page: 1 2 3 4 5 6 7 ... 55

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs636398	chr9:22680915-22680916	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs550488471	chr9:22680919-22680920	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs563921045	chr9:22680953-22680954	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs180865441	chr9:22680956-22680957	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs552739943	chr9:22680958-22680959	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs566180816	chr9:22680990-22680991	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs1448783	chr9:22680996-22680997	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs548572397	chr9:22680997-22680998	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs571073078	chr9:22681038-22681039	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs566981290	chr9:22681041-22681042	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs536191799	chr9:22681114-22681115	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs556016111	chr9:22681115-22681116	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs569547326	chr9:22681136-22681137	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs142642097	chr9:22681139-22681140	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs545056426	chr9:22681159-22681160	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs572107780	chr9:22681234-22681235	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs540731528	chr9:22681245-22681246	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs554593212	chr9:22681248-22681249	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs540009817	chr9:22681306-22681307	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs117849780	chr9:22681309-22681310	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs146917356	chr9:22681343-22681344	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs139340961	chr9:22681372-22681373	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs73446558	chr9:22681441-22681442	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs185466675	chr9:22681481-22681482	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs189883091	chr9:22681484-22681485	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs182205897	chr9:22681524-22681525	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs373341136	chr9:22681557-22681558	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs568142564	chr9:22681580-22681581	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs530797249	chr9:22681630-22681631	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs117993789	chr9:22681632-22681633	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs569633818	chr9:22681664-22681665	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs538495865	chr9:22681675-22681676	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs558722996	chr9:22681687-22681688	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs541471447	chr9:22681703-22681704	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs35281415	chr9:22681723-22681724	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs565730402	chr9:22681742-22681743	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs534765841	chr9:22681773-22681774	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs622693	chr9:22681776-22681777	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs140736156	chr9:22681789-22681790	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs187295059	chr9:22681808-22681809	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs111288706	chr9:22681843-22681844	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs191681357	chr9:22681865-22681866	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs577615670	chr9:22681871-22681872	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs150080075	chr9:22681883-22681884	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs138477221	chr9:22681907-22681908	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs537852877	chr9:22681913-22681914	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs528655405	chr9:22681973-22681974	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs113436654	chr9:22681977-22681978	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs561860655	chr9:22681978-22681979	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs4977792	chr9:22681982-22681983	Weak transcription Enhancers	n/a	n/a	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
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
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	21138945	CNVD
Adenoid cystic carcinoma	18332873	CNVD
Cancer	20581869	CNVD
Oral cancer	22144094	CNVD
Barrett''s syndrome	19417022	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Acute myeloid leukemia	21251322	CNVD
Oral cancer	21386901	CNVD
Breast cancer	21364760	CNVD
Acute myeloid leukemia	17237825	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Breast cancer	21858162	CNVD
Glioblastoma multiforme	21525872	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:111 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:22675200-22682800	Weak transcription	Liver	Liver
2	chr9:22678000-22681000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr9:22678400-22682000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr9:22679000-22687800	Weak transcription	Pancreas	Pancrea
5	chr9:22680800-22681600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr9:22681000-22683400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr9:22681000-22684800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
8	chr9:22681600-22683200	Enhancers	Pancreatic Islets	Pancreatic Islet
9	chr9:22681600-22683400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr9:22681800-22683000	Enhancers	Skeletal Muscle Female	skeletal muscle
11	chr9:22682000-22682600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr9:22682200-22683000	Enhancers	NHLF	lung
13	chr9:22682200-22683800	Enhancers	iPS-18 Cell Line	embryonic stem cell
14	chr9:22682200-22684800	Enhancers	Hela-S3	cervix
15	chr9:22682400-22682800	Enhancers	Skeletal Muscle Male	skeletal muscle
16	chr9:22682400-22682800	Enhancers	NHDF-Ad	bronchial
17	chr9:22682600-22683000	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
18	chr9:22682600-22683600	Enhancers	HUES6 Cell Line	embryonic stem cell
19	chr9:22682600-22683800	Enhancers	HUES48 Cell Line	embryonic stem cell
20	chr9:22682600-22684000	Enhancers	ES-I3 Cell Line	embryonic stem cell
21	chr9:22682600-22684200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
22	chr9:22682600-22684200	Enhancers	HMEC	breast
23	chr9:22682600-22684400	Enhancers	Muscle Satellite Cultured Cells	--
24	chr9:22682600-22684400	Enhancers	NH-A	brain
25	chr9:22682800-22683200	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
26	chr9:22682800-22683400	Weak transcription	NHDF-Ad	bronchial
27	chr9:22682800-22683600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
28	chr9:22682800-22683600	Enhancers	HSMM	muscle
29	chr9:22682800-22683600	Enhancers	HSMMtube	muscle
30	chr9:22682800-22684000	Enhancers	Duodenum Smooth Muscle	Duodenum
31	chr9:22682800-22684000	Enhancers	Osteobl	bone
32	chr9:22682800-22684200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
33	chr9:22682800-22685200	Strong transcription	Liver	Liver
34	chr9:22683000-22683200	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
35	chr9:22683000-22683200	Flanking Active TSS	NHLF	lung
36	chr9:22683000-22683400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
37	chr9:22683000-22684800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
38	chr9:22683200-22683400	Enhancers	NHLF	lung
39	chr9:22683200-22683600	Weak transcription	Pancreatic Islets	Pancreatic Islet
40	chr9:22683200-22683600	Active TSS	Skeletal Muscle Female	skeletal muscle
41	chr9:22683200-22684000	Enhancers	HUES64 Cell Line	embryonic stem cell
42	chr9:22683200-22684800	Enhancers	Skeletal Muscle Male	skeletal muscle
43	chr9:22683400-22683600	Flanking Active TSS	NHLF	lung
44	chr9:22683400-22683800	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
45	chr9:22683400-22683800	Active TSS	NHDF-Ad	bronchial
46	chr9:22683400-22684200	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
47	chr9:22683400-22684400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr9:22683600-22684000	Weak transcription	Skeletal Muscle Female	skeletal muscle
49	chr9:22683600-22684200	Enhancers	Pancreatic Islets	Pancreatic Islet
50	chr9:22683600-22685000	Enhancers	NHLF	lung

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