Variant report

Variant	nsv892807
Chromosome Location	chr9:24853876-25029338
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	chr9:24870645-24870801	H1-hESC	embryonic stem cell:	n/a	n/a
2	BHLHE40	chr9:24933214-24933331	GM12878	blood:	n/a	n/a
3	CEBPB	chr9:24969420-24969725	A549	lung:	n/a	chr9:24969572-24969583 chr9:24969572-24969581 chr9:24969570-24969583 chr9:24969570-24969581
4	CEBPB	chr9:24954743-24954943	H1-hESC	embryonic stem cell:	n/a	n/a
5	CEBPB	chr9:24997422-24997735	IMR90	lung:	n/a	chr9:24997567-24997580 chr9:24997567-24997578 chr9:24997567-24997580 chr9:24997567-24997580
6	CEBPB	chr9:25016672-25016872	H1-hESC	embryonic stem cell:	n/a	chr9:25016717-25016728
7	CEBPB	chr9:24997515-24997658	A549	lung:	n/a	chr9:24997567-24997580 chr9:24997567-24997578 chr9:24997567-24997580 chr9:24997567-24997580
8	CEBPB	chr9:24979415-24979650	A549	lung:	n/a	chr9:24979523-24979534
9	CEBPB	chr9:24932626-24932820	HepG2	liver:	n/a	chr9:24932795-24932807
10	CEBPB	chr9:25016586-25016879	IMR90	lung:	n/a	chr9:25016717-25016728
11	CEBPB	chr9:24949902-24950223	HepG2	liver:	n/a	chr9:24950042-24950053
12	CEBPB	chr9:24941624-24941826	HepG2	liver:	n/a	chr9:24941639-24941650
13	CEBPB	chr9:24949880-24950204	A549	lung:	n/a	chr9:24950042-24950053
14	CEBPB	chr9:25012655-25012930	HepG2	liver:	n/a	chr9:25012799-25012808 chr9:25012799-25012808 chr9:25012797-25012810 chr9:25012799-25012808 chr9:25012798-25012809 chr9:25012797-25012810 chr9:25012799-25012808 chr9:25012797-25012808
15	CEBPB	chr9:25012702-25012900	A549	lung:	n/a	chr9:25012799-25012808 chr9:25012799-25012808 chr9:25012797-25012810 chr9:25012799-25012808 chr9:25012798-25012809 chr9:25012797-25012810 chr9:25012799-25012808 chr9:25012797-25012808
16	CEBPB	chr9:24949921-24950217	IMR90	lung:	n/a	chr9:24950042-24950053
17	CEBPB	chr9:24979456-24979666	HepG2	liver:	n/a	chr9:24979523-24979534
18	CEBPB	chr9:24969394-24969744	HepG2	liver:	n/a	chr9:24969572-24969583 chr9:24969572-24969581 chr9:24969570-24969583 chr9:24969570-24969581
19	CEBPB	chr9:24997436-24997715	HepG2	liver:	n/a	chr9:24997567-24997580 chr9:24997567-24997578 chr9:24997567-24997580 chr9:24997567-24997580
20	CEBPB	chr9:24969424-24969755	IMR90	lung:	n/a	chr9:24969572-24969583 chr9:24969572-24969581 chr9:24969570-24969583 chr9:24969570-24969581
21	CEBPB	chr9:25016591-25016872	Hela-S3	cervix:	n/a	chr9:25016717-25016728
22	CEBPB	chr9:25016549-25016871	HepG2	liver:	n/a	chr9:25016717-25016728
23	CEBPB	chr9:24908150-24908241	HepG2	liver:	n/a	chr9:24908195-24908206
24	CEBPB	chr9:24969470-24969602	H1-hESC	embryonic stem cell:	n/a	chr9:24969572-24969583 chr9:24969572-24969581 chr9:24969570-24969583 chr9:24969570-24969581
25	CEBPB	chr9:24979380-24979631	IMR90	lung:	n/a	chr9:24979523-24979534
26	CHD2	chr9:25003842-25003971	GM12878	blood:	n/a	n/a
27	CHD2	chr9:25003696-25004054	H1-hESC	embryonic stem cell:	n/a	n/a
28	CTCF	chr9:25003840-25003990	GM12870	blood:	n/a	n/a
29	CTCF	chr9:25003638-25004093	H1-hESC	embryonic stem cell:	n/a	n/a
30	CTCF	chr9:24877760-24877910	GM06990	blood:	n/a	n/a
31	CTCF	chr9:25003900-25004050	GM12873	blood:	n/a	n/a
32	CTCF	chr9:25003700-25003850	GM12866	blood:	n/a	n/a
33	CTCF	chr9:25003881-25003899	GM19239	blood:	n/a	n/a
34	CTCF	chr9:25003760-25003910	HepG2	liver:	n/a	n/a
35	CTCF	chr9:25003840-25003990	GM12875	blood:	n/a	n/a
36	CTCF	chr9:24986320-24986470	NHEK	skin:	n/a	n/a
37	CTCF	chr9:25003820-25003970	WERI-Rb-1	eye:	n/a	n/a
38	CTCF	chr9:25003808-25004007	HepG2	liver:	n/a	n/a
39	CTCF	chr9:25003860-25004010	GM12872	blood:	n/a	n/a
40	CTCF	chr9:25003780-25003930	SK-N-SH_RA	brain:	n/a	n/a
41	CTCF	chr9:25003804-25003992	GM12878	blood:	n/a	n/a
42	CTCF	chr9:25003807-25004010	MCF-7	breast:	n/a	n/a
43	CTCF	chr9:25003860-25004010	GM12871	blood:	n/a	n/a
44	CTCF	chr9:25004160-25004310	HEK293	kidney:	n/a	n/a
45	CTCF	chr9:25003760-25003910	RPTEC	kidney:	n/a	n/a
46	CTCF	chr9:25003821-25003956	MCF-7	breast:	n/a	n/a
47	CTCF	chr9:25003760-25003910	Hela-S3	cervix:	n/a	n/a
48	CTCF	chr9:25003841-25003955	A549	lung:	n/a	n/a
49	CTCF	chr9:25003800-25003950	GM12874	blood:	n/a	n/a
50	CTCF	chr9:25003740-25003890	GM06990	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr8:43095024..43096022-chr9:24882323..24882823,2	MCF-7	breast:
2	chr2:88301087..88301608-chr9:24880154..24880654,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-IFT74-10	chr9:24905467-24905733	NONHSAT130497

Variant related genes	Relation type
RMRPP5	TF binding region
ENSG00000216088	TF binding region

Extended variants
information (count: 1409 )
Associated
traits (count: 145 )

Variant overlapped rSNPs/rCNVs (count:1409 , 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	rs113502801	chr9:24855612-24855613	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
2	rs533606401	chr9:24855640-24855641	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
3	rs146164783	chr9:24855644-24855645	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
4	rs560323551	chr9:24855656-24855657	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
5	rs78042205	chr9:24855665-24855666	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
6	rs542603323	chr9:24855672-24855673	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
7	rs562384015	chr9:24855727-24855728	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
8	rs533042375	chr9:24855729-24855730	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
9	rs192724687	chr9:24855730-24855731	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
10	rs564636464	chr9:24855746-24855747	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
11	rs10966502	chr9:24855762-24855763	Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs540859362	chr9:24855792-24855793	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
13	rs73642218	chr9:24873053-24873054	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs111440711	chr9:24875497-24875498	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs117398543	chr9:24875503-24875504	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs558754771	chr9:24875513-24875514	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs150230434	chr9:24875539-24875540	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs191525766	chr9:24875552-24875553	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs374515843	chr9:24875557-24875558	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs565971932	chr9:24875567-24875568	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs149358853	chr9:24875608-24875609	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs527296883	chr9:24875617-24875618	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs548385795	chr9:24875663-24875664	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs568028574	chr9:24875671-24875672	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs117969224	chr9:24877764-24877765	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs62570837	chr9:24877765-24877766	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs554753836	chr9:24877771-24877772	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs190708703	chr9:24877777-24877778	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs145183358	chr9:24879303-24879304	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs538441138	chr9:24879357-24879358	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs543012755	chr9:24879375-24879376	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs138961486	chr9:24879386-24879387	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs192147838	chr9:24879387-24879388	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs572030353	chr9:24879403-24879404	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs562617015	chr9:24879409-24879410	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs531673118	chr9:24879442-24879443	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs551887417	chr9:24879453-24879454	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs571542380	chr9:24879487-24879488	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs542734074	chr9:24879488-24879489	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs7850207	chr9:24879489-24879490	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs73481656	chr9:24879511-24879512	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs567575891	chr9:24879544-24879545	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs142027781	chr9:24879548-24879549	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs58742615	chr9:24879549-24879550	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs397961984	chr9:24879563-24879564	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs79994793	chr9:24879623-24879624	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs200686600	chr9:24879624-24879625	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs576004811	chr9:24879660-24879661	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs10966521	chr9:24879695-24879696	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs73642219	chr9:24879733-24879734	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:145)

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
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
Melanoma	17363583	CNVD
Adenoid cystic carcinoma	18332873	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	21858162	CNVD
Breast cancer	21364760	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Lung cancer	21569311	CNVD
Breast cancer	22522925	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:79 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:24855600-24855800	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
2	chr9:24879200-24880000	Enhancers	iPS-18 Cell Line	embryonic stem cell
3	chr9:24879200-24880200	Enhancers	HUES64 Cell Line	embryonic stem cell
4	chr9:24879200-24880600	Enhancers	iPS-20b Cell Line	embryonic stem cell
5	chr9:24879400-24880000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
6	chr9:24879600-24880400	Enhancers	HUES48 Cell Line	embryonic stem cell
7	chr9:24879600-24880400	Enhancers	Fetal Heart	heart
8	chr9:24879600-24882000	Enhancers	HMEC	breast
9	chr9:24879800-24882200	Enhancers	ES-I3 Cell Line	embryonic stem cell
10	chr9:24879800-24882200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
11	chr9:24880000-24880200	Enhancers	iPS-15b Cell Line	embryonic stem cell
12	chr9:24880000-24881000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
13	chr9:24880000-24881200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
14	chr9:24880200-24880800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr9:24880200-24881200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
16	chr9:24880200-24881600	Weak transcription	HUES64 Cell Line	embryonic stem cell
17	chr9:24880400-24880800	Weak transcription	HUES48 Cell Line	embryonic stem cell
18	chr9:24880600-24881000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
19	chr9:24880800-24882200	Enhancers	HUES48 Cell Line	embryonic stem cell
20	chr9:24881000-24882000	Enhancers	iPS-18 Cell Line	embryonic stem cell
21	chr9:24881000-24882200	Enhancers	iPS-20b Cell Line	embryonic stem cell
22	chr9:24881200-24881600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
23	chr9:24881200-24882000	Enhancers	iPS-15b Cell Line	embryonic stem cell
24	chr9:24881600-24882000	Enhancers	HUES64 Cell Line	embryonic stem cell
25	chr9:24881800-24882400	Enhancers	HUES6 Cell Line	embryonic stem cell
26	chr9:24897800-24898000	Enhancers	Gastric	stomach
27	chr9:24898400-24901800	Enhancers	Fetal Heart	heart
28	chr9:24901800-24907400	Weak transcription	Fetal Heart	heart
29	chr9:24907400-24907800	Enhancers	Fetal Heart	heart
30	chr9:24908400-24908800	Enhancers	H1 Cell Line	embryonic stem cell
31	chr9:24908400-24908800	Enhancers	HUES48 Cell Line	embryonic stem cell
32	chr9:24908800-24909200	Enhancers	HUES64 Cell Line	embryonic stem cell
33	chr9:24908800-24909800	Weak transcription	HUES48 Cell Line	embryonic stem cell
34	chr9:24909800-24910600	Enhancers	iPS-18 Cell Line	embryonic stem cell
35	chr9:24909800-24911200	Enhancers	HUES48 Cell Line	embryonic stem cell
36	chr9:24910000-24910600	Enhancers	iPS-15b Cell Line	embryonic stem cell
37	chr9:24910200-24911000	Enhancers	ES-I3 Cell Line	embryonic stem cell
38	chr9:24910400-24910600	Enhancers	H1 Cell Line	embryonic stem cell
39	chr9:24911800-24912400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
40	chr9:24911800-24913600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
41	chr9:24931400-24932800	Enhancers	Primary B cells from cord blood	blood
42	chr9:24932600-24933200	Enhancers	GM12878-XiMat	blood
43	chr9:24932800-24933200	Flanking Active TSS	Primary B cells from cord blood	blood
44	chr9:24933200-24935000	Enhancers	Primary B cells from cord blood	blood
45	chr9:24936200-24936600	Enhancers	iPS-15b Cell Line	embryonic stem cell
46	chr9:24936400-24936600	Enhancers	HUES6 Cell Line	embryonic stem cell
47	chr9:24936600-24939000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
48	chr9:24936800-24940800	Weak transcription	HUES6 Cell Line	embryonic stem cell
49	chr9:24938800-24939600	Enhancers	iPS-20b Cell Line	embryonic stem cell
50	chr9:24938800-24940000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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