Variant report

Variant	nsv1036317
Chromosome Location	chr10:43189367-43253587
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	ATF1	chr10:43239265-43239373	K562	blood:	n/a	n/a
2	ATF1	chr10:43234242-43234371	K562	blood:	n/a	n/a
3	BACH1	chr10:43248608-43248903	H1-hESC	embryonic stem cell:	n/a	n/a
4	BATF	chr10:43218973-43219261	GM12878	blood:	n/a	n/a
5	BHLHE40	chr10:43249101-43249382	K562	blood:	n/a	n/a
6	BRCA1	chr10:43248663-43248943	H1-hESC	embryonic stem cell:	n/a	n/a
7	CBX3	chr10:43237046-43237288	K562	blood:	n/a	n/a
8	CBX3	chr10:43236980-43237313	K562	blood:	n/a	n/a
9	CCNT2	chr10:43248619-43248819	K562	blood:	n/a	n/a
10	CEBPB	chr10:43204367-43204575	HepG2	liver:	n/a	chr10:43204513-43204524 chr10:43204512-43204525
11	CEBPB	chr10:43230108-43230288	K562	blood:	n/a	n/a
12	CEBPB	chr10:43239152-43239453	K562	blood:	n/a	chr10:43239295-43239306
13	CEBPB	chr10:43195023-43195204	K562	blood:	n/a	n/a
14	CEBPB	chr10:43239164-43239414	K562	blood:	n/a	chr10:43239295-43239306
15	CEBPB	chr10:43230096-43230321	MCF-7	breast:	n/a	n/a
16	CEBPB	chr10:43239156-43239359	HepG2	liver:	n/a	chr10:43239295-43239306
17	CHD2	chr10:43250997-43251011	HepG2	liver:	n/a	n/a
18	CHD2	chr10:43248662-43248941	H1-hESC	embryonic stem cell:	n/a	chr10:43248745-43248752
19	CHD2	chr10:43249795-43250076	H1-hESC	embryonic stem cell:	n/a	n/a
20	CREB1	chr10:43248525-43248894	H1-hESC	embryonic stem cell:	n/a	n/a
21	CREB1	chr10:43248462-43249010	H1-hESC	embryonic stem cell:	n/a	n/a
22	CREB1	chr10:43248635-43249012	A549	lung:	n/a	n/a
23	CTBP2	chr10:43248525-43249930	H1-hESC	embryonic stem cell:	n/a	n/a
24	CTCF	chr10:43220104-43220263	K562	blood:	n/a	chr10:43220223-43220232
25	CTCF	chr10:43250720-43250870	HCPEpiC	choroid plexus:	n/a	chr10:43250833-43250842
26	CTCF	chr10:43220211-43220224	LNCaP	prostate:	n/a	n/a
27	CTCF	chr10:43249900-43250050	GM12873	blood:	n/a	n/a
28	CTCF	chr10:43251294-43251456	K562	blood:	n/a	n/a
29	CTCF	chr10:43250860-43251010	AG04449	skin:	n/a	n/a
30	CTCF	chr10:43250780-43250930	HBMEC	blood vessel:	n/a	chr10:43250833-43250842
31	CTCF	chr10:43248740-43248890	HCFaa	heart:	n/a	chr10:43248777-43248793 chr10:43248779-43248792
32	CTCF	chr10:43250780-43250930	A549	lung:	n/a	chr10:43250833-43250842
33	CTCF	chr10:43249840-43249990	GM12868	blood:	n/a	chr10:43249860-43249873
34	CTCF	chr10:43248700-43248850	SK-N-SH_RA	brain:	n/a	chr10:43248777-43248793 chr10:43248779-43248792
35	CTCF	chr10:43248474-43249056	HCT-116	colon:	n/a	chr10:43248777-43248793 chr10:43248779-43248792
36	CTCF	chr10:43248680-43248830	GM12869	blood:	n/a	chr10:43248777-43248793 chr10:43248779-43248792
37	CTCF	chr10:43248647-43248920	Pancreas_OC	pancreas:	n/a	chr10:43248777-43248793 chr10:43248779-43248792
38	CTCF	chr10:43250740-43250890	HMEC	breast:	n/a	chr10:43250833-43250842
39	CTCF	chr10:43249820-43249970	HMEC	breast:	n/a	chr10:43249860-43249873
40	CTCF	chr10:43239760-43239910	K562	blood:	n/a	n/a
41	CTCF	chr10:43248700-43248850	GM12871	blood:	n/a	chr10:43248777-43248793 chr10:43248779-43248792
42	CTCF	chr10:43248700-43248850	GM06990	blood:	n/a	chr10:43248777-43248793 chr10:43248779-43248792
43	CTCF	chr10:43249085-43249094	Lung_OC	lung:	n/a	n/a
44	CTCF	chr10:43248608-43248959	GM12878	blood:	n/a	chr10:43248777-43248793 chr10:43248779-43248792
45	CTCF	chr10:43248689-43248843	GM19239	blood:	n/a	chr10:43248777-43248793 chr10:43248779-43248792
46	CTCF	chr10:43248680-43248830	GM12867	blood:	n/a	chr10:43248777-43248793 chr10:43248779-43248792
47	CTCF	chr10:43248683-43248899	A549	lung:	n/a	chr10:43248777-43248793 chr10:43248779-43248792
48	CTCF	chr10:43248661-43248919	LNCaP	prostate:	n/a	chr10:43248777-43248793 chr10:43248779-43248792
49	CTCF	chr10:43250720-43250870	AG04449	skin:	n/a	chr10:43250833-43250842
50	CTCF	chr10:43202842-43202909	GM12878	blood:	n/a	chr10:43202853-43202874 chr10:43202859-43202875 chr10:43202858-43202876

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:43215944-43215994	T-47D	breast:	n/a
2	chr10:43215944-43215994	T-47D	breast:	n/a
3	chr10:43250063-43250113	NHBE	bronchial:	n/a
4	chr10:43249924-43249974	AG09319	gingival:	n/a
5	chr10:43249924-43249974	IMR90	lung:	fetal
6	chr10:43251951-43252001	Jurkat	blood:	n/a
7	chr10:43250569-43250619	NT2-D1	testis:	n/a
8	chr10:43245080-43245130	HEEpiC	esophagus:	n/a
9	chr10:43250800-43250850	MCF-7	breast:	n/a
10	chr10:43215944-43215994	H1-hESC	embryonic stem cell:	embryo
11	chr10:43249161-43249211	AG09319	gingival:	n/a
12	chr10:43245080-43245130	U87	brain:	n/a
13	chr10:43250800-43250850	HL-60	blood:	n/a
14	chr10:43249924-43249974	AG10803	skin:	n/a
15	chr10:43209934-43209984	HPAEpiC	pulmonary alveolar:	n/a
16	chr10:43209934-43209984	AG04450	lung:	fetal
17	chr10:43247938-43247988	HPAEpiC	pulmonary alveolar:	n/a
18	chr10:43216927-43216977	HepG2	liver:	n/a
19	chr10:43247938-43247988	HMEC	breast:	n/a
20	chr10:43252305-43252355	HRCEpiC	kidney:	n/a
21	chr10:43249161-43249211	Jurkat	blood:	n/a
22	chr10:43216927-43216977	Caco-2	colon:	n/a
23	chr10:43209934-43209984	NT2-D1	testis:	n/a
24	chr10:43251951-43252001	SK-N-SH_RA	brain:	n/a
25	chr10:43251951-43252001	HEEpiC	esophagus:	n/a
26	chr10:43247938-43247988	ECC-1	luminal epithelium:	n/a
27	chr10:43252305-43252355	PANC-1	pancreas:	n/a
28	chr10:43252305-43252355	MCF10A-Er-Src	breast:	n/a
29	chr10:43249161-43249211	AG10803	skin:	n/a
30	chr10:43251951-43252001	AG09319	gingival:	n/a
31	chr10:43209934-43209984	SK-N-MC	brain:	n/a
32	chr10:43251951-43252001	BJ	skin:	n/a
33	chr10:43245080-43245130	CMK	blood:	n/a
34	chr10:43247938-43247988	NH-A	brain:	n/a
35	chr10:43245080-43245130	Jurkat	blood:	n/a
36	chr10:43249161-43249211	CMK	blood:	n/a
37	chr10:43245080-43245130	BE2_C	brain:	n/a
38	chr10:43249161-43249211	ECC-1	luminal epithelium:	n/a
39	chr10:43249924-43249974	HCF	heart:	n/a
40	chr10:43215944-43215994	AG04450	lung:	fetal
41	chr10:43209934-43209984	Hepatocyte	liver:	n/a
42	chr10:43250569-43250619	HCM	heart:	n/a
43	chr10:43250063-43250113	HAEpiC	amniotic membrane:	n/a
44	chr10:43216927-43216977	HIPEpiC	eye:	n/a
45	chr10:43247938-43247988	U87	brain:	n/a
46	chr10:43216927-43216977	GM12892	blood:	n/a
47	chr10:43252305-43252355	GM12891	blood:	n/a
48	chr10:43248870-43248920	HPAEpiC	pulmonary alveolar:	n/a
49	chr10:43249161-43249211	HAEpiC	amniotic membrane:	n/a
50	chr10:43215944-43215994	AoSMC	blood vessel:	n/a

No.	Distal block	Cell Line	Cell type
1	chr10:43132391..43135100-chr10:43189606..43191108,2	MCF-7	breast:
2	chr10:43251549..43254175-chr10:43277144..43279429,2	K562	blood:
3	chr10:43253135..43254665-chr10:43264247..43266986,2	MCF-7	breast:
4	chr10:43203133..43206798-chr10:43276930..43278950,3	MCF-7	breast:
5	chr10:43245352..43247530-chr10:43276802..43279739,2	K562	blood:
6	chr10:43250283..43253153-chr10:43277432..43279955,3	MCF-7	breast:
7	chr10:43228372..43230638-chr10:43276090..43278496,2	MCF-7	breast:
8	chr10:43250846..43253793-chr10:43254051..43256963,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-BMS1-4	chr10:43236053-43236103	NONHSAT012928
2	lnc-BMS1-2	chr10:43191483-43191659	ENSG00000234864
3	lnc-BMS1-2	chr10:43198870-43201901	ENSG00000234864
4	lnc-BMS1-4	chr10:43237124-43237260	NONHSAT012928
5	lnc-BMS1-2	chr10:43196950-43197705	ENSG00000234864
6	lnc-ZNF33B-2	chr10:43246626-43247593	ENSG00000259869.1
7	lnc-BMS1-4	chr10:43236406-43236520	NONHSAT012928

Variant related genes	Relation type
ENSG00000259869	TF binding region
ENSG00000234864	TF binding region
ENSG00000233515	TF binding region
RSU1P1	TF binding region
DUXAP3	TF binding region
CUBNP1	TF binding region
ENSG00000259869	CpG island
ENSG00000234864	CpG island
ENSG00000233515	CpG island
RSU1P1	CpG island
DUXAP3	CpG island
CUBNP1	CpG island
ENSG00000272373	chromatin interactions
ENSG00000165733	chromatin interactions
ENSG00000196693	chromatin interactions

Extended variants
information (count: 1638 )
Associated
traits (count: 56 )

Variant overlapped rSNPs/rCNVs (count:1638 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs542186512	chr10:43189371-43189372	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
2	rs189935332	chr10:43189381-43189382	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
3	rs371904411	chr10:43189387-43189388	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
4	rs554443249	chr10:43189460-43189461	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
5	rs150578919	chr10:43189495-43189496	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
6	rs139257147	chr10:43189500-43189501	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
7	rs549004484	chr10:43189533-43189534	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
8	rs567595122	chr10:43189538-43189539	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
9	rs368585685	chr10:43189598-43189599	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
10	rs547003244	chr10:43189603-43189604	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
11	rs144308093	chr10:43189636-43189637	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs572438234	chr10:43189640-43189641	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs546227290	chr10:43189641-43189642	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs539093186	chr10:43189663-43189664	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs181529384	chr10:43189666-43189667	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs569468089	chr10:43189692-43189693	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs12262615	chr10:43189707-43189708	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs207470827	chr10:43189709-43189710	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs185914676	chr10:43189713-43189714	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs573507691	chr10:43189725-43189726	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs112146402	chr10:43189729-43189730	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs552515706	chr10:43189754-43189755	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs577229609	chr10:43189755-43189756	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs544659303	chr10:43189760-43189761	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs376326243	chr10:43189791-43189792	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs531755877	chr10:43189793-43189794	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs530610959	chr10:43189800-43189801	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs143831194	chr10:43189828-43189829	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs561768604	chr10:43189829-43189830	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs528361701	chr10:43189837-43189838	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs546595641	chr10:43189838-43189839	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs529164474	chr10:43189839-43189840	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs571620677	chr10:43189852-43189853	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs146854354	chr10:43189869-43189870	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs190715802	chr10:43189871-43189872	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs182037290	chr10:43189916-43189917	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs112586108	chr10:43189925-43189926	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs185010339	chr10:43189926-43189927	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs536424022	chr10:43189927-43189928	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs576032599	chr10:43189939-43189940	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs555115698	chr10:43189971-43189972	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs201090960	chr10:43189979-43189980	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs566965864	chr10:43190089-43190090	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs534465747	chr10:43190095-43190096	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs558828945	chr10:43190140-43190141	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs577215582	chr10:43190150-43190151	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs190883351	chr10:43190199-43190200	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs148336200	chr10:43190215-43190216	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs548277539	chr10:43190222-43190223	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs556625209	chr10:43190288-43190289	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:56)

Disease	PMID	Source
Pancreatic endocrine tumor	17639061	CNVD
Gastric cancer	17908304	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Melanoma	18172304	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Lung cancer	18438408	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Ewing''s sarcoma	17952124	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	20724749	CNVD
Autism	22495311	CNVD
Esophageal cancer	21851588	CNVD
Prostate cancer	18632612	CNVD
Autism	18414403	CNVD
Cockayne syndrome	18421352	CNVD
Glioblastoma	16823260	CNVD
Medulloblastoma	16968546	CNVD
Neuroblastoma	17533364	CNVD
Mental retardation	21062444	CNVD
Cancer	21183584	CNVD
T-cell lymphomas	19863542	CNVD
Testicular germ cell tumor	18059402	CNVD
Squamous cell cancer	21044232	CNVD
Glioma	21971842	CNVD
Cancer	21637783	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	22241247	CNVD
Intellectual disability	21811512	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Obesity	21956041	CNVD
Renal cell carcinoma	18765545	CNVD
Breast cancer	21785460	CNVD
Autism	20531469	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Ovarian cancer	21781307	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Melanoma	20877625	CNVD

Chromatin state (count:475 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:43186200-43190400	Weak transcription	Pancreas	Pancrea
2	chr10:43190000-43191600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr10:43190200-43191400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
4	chr10:43190600-43191200	Enhancers	HepG2	liver
5	chr10:43190800-43191200	Enhancers	Liver	Liver
6	chr10:43190800-43191600	Enhancers	K562	blood
7	chr10:43191400-43193400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr10:43191600-43193000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr10:43193000-43193600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chr10:43193400-43193600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
11	chr10:43193600-43194000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
12	chr10:43194000-43194400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
13	chr10:43194200-43194600	Enhancers	ES-I3 Cell Line	embryonic stem cell
14	chr10:43202600-43202800	Enhancers	Pancreatic Islets	Pancreatic Islet
15	chr10:43202800-43203600	Active TSS	Pancreatic Islets	Pancreatic Islet
16	chr10:43212600-43213000	Enhancers	Spleen	Spleen
17	chr10:43212800-43213000	Enhancers	HepG2	liver
18	chr10:43213000-43215800	Weak transcription	Spleen	Spleen
19	chr10:43215800-43216200	ZNF genes & repeats	Spleen	Spleen
20	chr10:43217600-43218000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
21	chr10:43227800-43228000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
22	chr10:43227800-43228000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
23	chr10:43230000-43230400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr10:43232600-43235200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
25	chr10:43233200-43235600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
26	chr10:43235200-43235400	Enhancers	Gastric	stomach
27	chr10:43241400-43241600	Enhancers	K562	blood
28	chr10:43241600-43242400	Active TSS	K562	blood
29	chr10:43248000-43248200	Active TSS	Duodenum Mucosa	Duodenum
30	chr10:43248000-43248800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
31	chr10:43248200-43248400	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
32	chr10:43248200-43248400	Bivalent/Poised TSS	Primary hematopoietic stem cells short term culture	blood
33	chr10:43248200-43248400	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
34	chr10:43248200-43248400	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin01	Skin
35	chr10:43248200-43248400	Enhancers	Adipose Nuclei	Adipose
36	chr10:43248200-43248400	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
37	chr10:43248200-43248400	Bivalent Enhancer	Fetal Intestine Small	intestine
38	chr10:43248200-43248400	Enhancers	Pancreas	Pancrea
39	chr10:43248200-43248400	Bivalent Enhancer	Rectal Mucosa Donor 31	rectum
40	chr10:43248200-43248400	Bivalent/Poised TSS	Right Ventricle	heart
41	chr10:43248200-43248400	Bivalent Enhancer	Stomach Smooth Muscle	stomach
42	chr10:43248200-43248600	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
43	chr10:43248200-43248600	Bivalent Enhancer	Primary T helper naive cells fromperipheralblood	blood
44	chr10:43248200-43248600	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin02	Skin
45	chr10:43248200-43248600	Flanking Active TSS	Duodenum Mucosa	Duodenum
46	chr10:43248200-43248600	Flanking Bivalent TSS/Enh	Placenta	Placenta
47	chr10:43248200-43248600	Bivalent/Poised TSS	HUVEC	blood vessel
48	chr10:43248200-43248800	Bivalent/Poised TSS	Duodenum Smooth Muscle	Duodenum
49	chr10:43248200-43248800	Bivalent Enhancer	Stomach Mucosa	stomach
50	chr10:43248200-43249000	Active TSS	A549	lung

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