Variant report

Variant	esv2764213
Chromosome Location	chr10:43183225-43251704
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:689)
CpG islands
(count:1102)
Chromatin interactive
region (count:9)
LncRNA
region (count:12)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:689 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

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	chr10:43239156-43239359	HepG2	liver:	n/a	chr10:43239295-43239306
11	CEBPB	chr10:43230108-43230288	K562	blood:	n/a	n/a
12	CEBPB	chr10:43204367-43204575	HepG2	liver:	n/a	chr10:43204513-43204524 chr10:43204512-43204525
13	CEBPB	chr10:43239164-43239414	K562	blood:	n/a	chr10:43239295-43239306
14	CEBPB	chr10:43230096-43230321	MCF-7	breast:	n/a	n/a
15	CEBPB	chr10:43239152-43239453	K562	blood:	n/a	chr10:43239295-43239306
16	CEBPB	chr10:43195023-43195204	K562	blood:	n/a	n/a
17	CHD2	chr10:43249795-43250076	H1-hESC	embryonic stem cell:	n/a	n/a
18	CHD2	chr10:43248662-43248941	H1-hESC	embryonic stem cell:	n/a	chr10:43248745-43248752
19	CHD2	chr10:43250997-43251011	HepG2	liver:	n/a	n/a
20	CREB1	chr10:43248635-43249012	A549	lung:	n/a	n/a
21	CREB1	chr10:43248462-43249010	H1-hESC	embryonic stem cell:	n/a	n/a
22	CREB1	chr10:43248525-43248894	H1-hESC	embryonic stem cell:	n/a	n/a
23	CTBP2	chr10:43248525-43249930	H1-hESC	embryonic stem cell:	n/a	n/a
24	CTCF	chr10:43227840-43227846	MCF-7	breast:	n/a	n/a
25	CTCF	chr10:43248720-43248870	RPTEC	kidney:	n/a	chr10:43248777-43248793 chr10:43248779-43248792
26	CTCF	chr10:43250740-43250890	WERI-Rb-1	eye:	n/a	chr10:43250833-43250842
27	CTCF	chr10:43249760-43249910	GM12873	blood:	n/a	chr10:43249860-43249873
28	CTCF	chr10:43242232-43242249	GM10266	blood:	n/a	n/a
29	CTCF	chr10:43185800-43185950	HepG2	liver:	n/a	n/a
30	CTCF	chr10:43248400-43248550	AoAF	blood vessel:	n/a	n/a
31	CTCF	chr10:43249880-43250030	HEEpiC	esophagus:	n/a	n/a
32	CTCF	chr10:43248620-43248912	ProgFib	skin:	n/a	chr10:43248777-43248793 chr10:43248779-43248792
33	CTCF	chr10:43248600-43248997	K562	blood:	n/a	chr10:43248777-43248793 chr10:43248779-43248792
34	CTCF	chr10:43248440-43248590	HRE	kidney:	n/a	n/a
35	CTCF	chr10:43250820-43250970	HCT-116	colon:	n/a	chr10:43250833-43250842
36	CTCF	chr10:43248260-43248410	NHDF-neo	bronchial:	n/a	n/a
37	CTCF	chr10:43248740-43248890	AG09309	skin:	n/a	chr10:43248777-43248793 chr10:43248779-43248792
38	CTCF	chr10:43239700-43239850	SK-N-SH_RA	brain:	n/a	n/a
39	CTCF	chr10:43248680-43248830	GM12866	blood:	n/a	chr10:43248777-43248793 chr10:43248779-43248792
40	CTCF	chr10:43250740-43250890	GM12871	blood:	n/a	chr10:43250833-43250842
41	CTCF	chr10:43248380-43248530	HCPEpiC	choroid plexus:	n/a	n/a
42	CTCF	chr10:43248630-43248898	ECC-1	luminal epithelium:	n/a	chr10:43248777-43248793 chr10:43248779-43248792
43	CTCF	chr10:43239800-43239950	RPTEC	kidney:	n/a	n/a
44	CTCF	chr10:43248638-43248917	GM19238	blood:	n/a	chr10:43248777-43248793 chr10:43248779-43248792
45	CTCF	chr10:43250900-43251050	GM12873	blood:	n/a	n/a
46	CTCF	chr10:43249760-43249910	SK-N-SH_RA	brain:	n/a	chr10:43249860-43249873
47	CTCF	chr10:43239720-43239870	SK-N-SH_RA	brain:	n/a	n/a
48	CTCF	chr10:43250760-43250910	BJ	skin:	n/a	chr10:43250833-43250842
49	CTCF	chr10:43239660-43239810	AoAF	blood vessel:	n/a	n/a
50	CTCF	chr10:43250740-43250890	AG09319	gingival:	n/a	chr10:43250833-43250842

(count:1102 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:43187184-43187234	HUVEC	blood vessel:	n/a
2	chr10:43209934-43209984	SK-N-MC	brain:	n/a
3	chr10:43216927-43216977	MCF-7	breast:	n/a
4	chr10:43248870-43248920	HUVEC	blood vessel:	n/a
5	chr10:43187184-43187234	HUVEC	blood vessel:	n/a
6	chr10:43209934-43209984	SK-N-MC	brain:	n/a
7	chr10:43216927-43216977	MCF-7	breast:	n/a
8	chr10:43248870-43248920	HUVEC	blood vessel:	n/a
9	chr10:43249924-43249974	SKMC	muscle:	n/a
10	chr10:43247938-43247988	HUVEC	blood vessel:	n/a
11	chr10:43186900-43186950	HEEpiC	esophagus:	n/a
12	chr10:43187175-43187225	SKMC	muscle:	n/a
13	chr10:43245080-43245130	HCPEpiC	choroid plexus:	n/a
14	chr10:43187321-43187371	NHDF-neo	bronchial:	n/a
15	chr10:43248870-43248920	Hepatocyte	liver:	n/a
16	chr10:43209934-43209984	HIPEpiC	eye:	n/a
17	chr10:43249924-43249974	GM12892	blood:	n/a
18	chr10:43245080-43245130	SK-N-SH	brain:	n/a
19	chr10:43209934-43209984	HPAEpiC	pulmonary alveolar:	n/a
20	chr10:43186868-43186918	AG09309	skin:	n/a
21	chr10:43215944-43215994	HPAEpiC	pulmonary alveolar:	n/a
22	chr10:43187184-43187234	HRPEpiC	eye:	n/a
23	chr10:43249161-43249211	SK-N-MC	brain:	n/a
24	chr10:43209934-43209984	SK-N-SH	brain:	n/a
25	chr10:43216927-43216977	HepG2	liver:	n/a
26	chr10:43216927-43216977	HL-60	blood:	n/a
27	chr10:43186868-43186918	MCF10A-Er-Src	breast:	n/a
28	chr10:43186810-43186860	PFSK-1	brain:	n/a
29	chr10:43186900-43186950	HepG2	liver:	n/a
30	chr10:43215944-43215994	HNPCEpiC	eye:	n/a
31	chr10:43209934-43209984	HCF	heart:	n/a
32	chr10:43250063-43250113	HCT-116	colon:	n/a
33	chr10:43248870-43248920	NB4	blood:	n/a
34	chr10:43250063-43250113	AG10803	skin:	n/a
35	chr10:43187321-43187371	ovcar-3	ovarian:	n/a
36	chr10:43249161-43249211	HEK293	kidney:	embryo
37	chr10:43186810-43186860	LNCaP	prostate:	n/a
38	chr10:43186810-43186860	HL-60	blood:	n/a
39	chr10:43245080-43245130	HRCEpiC	kidney:	n/a
40	chr10:43250569-43250619	LNCaP	prostate:	n/a
41	chr10:43209934-43209984	GM12878	blood:	n/a
42	chr10:43215944-43215994	HIPEpiC	eye:	n/a
43	chr10:43249924-43249974	BE2_C	brain:	n/a
44	chr10:43245080-43245130	HNPCEpiC	eye:	n/a
45	chr10:43186900-43186950	NH-A	brain:	n/a
46	chr10:43250800-43250850	Jurkat	blood:	n/a
47	chr10:43187321-43187371	PANC-1	pancreas:	n/a
48	chr10:43186900-43186950	GM06990	blood:	n/a
49	chr10:43248870-43248920	IMR90	lung:	fetal
50	chr10:43209934-43209984	HAEpiC	amniotic membrane:	n/a

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr10:43203133..43206798-chr10:43276930..43278950,3	MCF-7	breast:
2	chr10:43132391..43135100-chr10:43189606..43191108,2	MCF-7	breast:
3	chr10:43245352..43247530-chr10:43276802..43279739,2	K562	blood:
4	chr10:43132526..43135261-chr10:43184647..43186574,3	MCF-7	breast:
5	chr10:43251549..43254175-chr10:43277144..43279429,2	K562	blood:
6	chr10:43179370..43182447-chr10:43184174..43186310,3	MCF-7	breast:
7	chr10:43250846..43253793-chr10:43254051..43256963,2	K562	blood:
8	chr10:43228372..43230638-chr10:43276090..43278496,2	MCF-7	breast:
9	chr10:43250283..43253153-chr10:43277432..43279955,3	MCF-7	breast:

(count:12 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-BMS1-4	chr10:43237124-43237260	NONHSAT012928
2	lnc-ZNF33B-1	chr10:43186987-43187198	NONHSAT012922
3	lnc-ZNF33B-1	chr10:43186983-43187171	ENSG00000233515
4	lnc-ZNF33B-1	chr10:43186983-43187198	NONHSAT012921
5	lnc-BMS1-2	chr10:43196950-43197705	ENSG00000234864
6	lnc-ZNF33B-1	chr10:43187438-43187527	NONHSAT012924
7	lnc-ZNF33B-1	chr10:43186181-43186249	NONHSAT139966
8	lnc-BMS1-4	chr10:43236406-43236520	NONHSAT012928
9	lnc-BMS1-4	chr10:43236053-43236103	NONHSAT012928
10	lnc-BMS1-2	chr10:43191483-43191659	ENSG00000234864
11	lnc-BMS1-2	chr10:43198870-43201901	ENSG00000234864
12	lnc-ZNF33B-2	chr10:43246626-43247593	ENSG00000259869.1

No data

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
ENSG00000196693	chromatin interactions
ENSG00000165733	chromatin interactions
ENSG00000272373	chromatin interactions

Extended variants
information (count: 1876 )
Associated
traits (count: 55 )

Variant overlapped rSNPs/rCNVs (count:1876 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2473114	chr10:43183225-43183226	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs182321207	chr10:43183228-43183229	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs547046673	chr10:43183244-43183245	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs530065066	chr10:43183264-43183265	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs370335047	chr10:43183291-43183292	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs373878041	chr10:43183296-43183297	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs530530831	chr10:43183321-43183322	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs572158147	chr10:43183334-43183335	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs113418400	chr10:43183338-43183339	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs370635605	chr10:43183352-43183353	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs576291279	chr10:43183379-43183380	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs372396204	chr10:43183395-43183396	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs186039706	chr10:43183399-43183400	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs376289143	chr10:43183414-43183415	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs573710457	chr10:43183424-43183425	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs188409231	chr10:43183534-43183535	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs559597288	chr10:43183581-43183582	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs115790125	chr10:43183652-43183653	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs529242615	chr10:43183653-43183654	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs551730253	chr10:43183656-43183657	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs148015177	chr10:43183719-43183720	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs531260066	chr10:43183732-43183733	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs141694026	chr10:43183742-43183743	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs181173987	chr10:43183768-43183769	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs528900063	chr10:43183773-43183774	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs371101630	chr10:43183891-43183892	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs547464911	chr10:43183893-43183894	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs565677845	chr10:43183894-43183895	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs539602566	chr10:43183906-43183907	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs185592771	chr10:43183909-43183910	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs569533147	chr10:43183916-43183917	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs536909432	chr10:43183968-43183969	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs555253711	chr10:43183971-43183972	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs573655053	chr10:43183977-43183978	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs71505639	chr10:43183986-43183987	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs183493434	chr10:43184005-43184006	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs386743138	chr10:43184030-43184031	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs114796990	chr10:43184031-43184032	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs150526925	chr10:43184042-43184043	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs568273147	chr10:43184056-43184057	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs535381023	chr10:43184067-43184068	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs374579222	chr10:43184109-43184110	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs561614218	chr10:43184146-43184147	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs528885422	chr10:43184163-43184164	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs112409437	chr10:43184171-43184172	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs35689174	chr10:43184172-43184173	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs186762969	chr10:43184184-43184185	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs58116228	chr10:43184186-43184187	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs565743959	chr10:43184198-43184199	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs569213852	chr10:43184201-43184202	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:55)

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

Chromatin state (count:482 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:43182800-43184200	Enhancers	Stomach Mucosa	stomach
2	chr10:43183200-43183800	Weak transcription	K562	blood
3	chr10:43183800-43184000	Enhancers	K562	blood
4	chr10:43183800-43184200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
5	chr10:43184000-43185200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
6	chr10:43184400-43185000	Enhancers	Primary T helper cells PMA-I stimulated	--
7	chr10:43184400-43185600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr10:43184600-43185400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
9	chr10:43184600-43185600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
10	chr10:43184600-43185600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr10:43185600-43186200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
12	chr10:43185600-43186600	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr10:43185800-43186200	Enhancers	Pancreas	Pancrea
14	chr10:43186200-43190400	Weak transcription	Pancreas	Pancrea
15	chr10:43186600-43187000	Strong transcription	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr10:43187000-43187200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr10:43187200-43187400	Strong transcription	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr10:43187400-43188800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr10:43190000-43191600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
20	chr10:43190200-43191400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
21	chr10:43190600-43191200	Enhancers	HepG2	liver
22	chr10:43190800-43191200	Enhancers	Liver	Liver
23	chr10:43190800-43191600	Enhancers	K562	blood
24	chr10:43191400-43193400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
25	chr10:43191600-43193000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
26	chr10:43193000-43193600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
27	chr10:43193400-43193600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
28	chr10:43193600-43194000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
29	chr10:43194000-43194400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
30	chr10:43194200-43194600	Enhancers	ES-I3 Cell Line	embryonic stem cell
31	chr10:43202600-43202800	Enhancers	Pancreatic Islets	Pancreatic Islet
32	chr10:43202800-43203600	Active TSS	Pancreatic Islets	Pancreatic Islet
33	chr10:43212600-43213000	Enhancers	Spleen	Spleen
34	chr10:43212800-43213000	Enhancers	HepG2	liver
35	chr10:43213000-43215800	Weak transcription	Spleen	Spleen
36	chr10:43215800-43216200	ZNF genes & repeats	Spleen	Spleen
37	chr10:43217600-43218000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
38	chr10:43227800-43228000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
39	chr10:43227800-43228000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr10:43230000-43230400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chr10:43232600-43235200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
42	chr10:43233200-43235600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
43	chr10:43235200-43235400	Enhancers	Gastric	stomach
44	chr10:43241400-43241600	Enhancers	K562	blood
45	chr10:43241600-43242400	Active TSS	K562	blood
46	chr10:43248000-43248200	Active TSS	Duodenum Mucosa	Duodenum
47	chr10:43248000-43248800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
48	chr10:43248200-43248400	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
49	chr10:43248200-43248400	Bivalent/Poised TSS	Primary hematopoietic stem cells short term culture	blood
50	chr10:43248200-43248400	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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