Variant report

Variant	nsv1026224
Chromosome Location	chr7:5843430-5907661
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1275)
CpG islands
(count:1221)
Chromatin interactive
region (count:13)
LncRNA
region (count:16)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1275 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:5862273-5862605	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:5867592-5867694	HepG2	liver:	n/a	n/a
3	ARID3A	chr7:5862528-5862814	K562	blood:	n/a	n/a
4	ARID3A	chr7:5867459-5867694	K562	blood:	n/a	n/a
5	ATF1	chr7:5862457-5862892	K562	blood:	n/a	n/a
6	ATF2	chr7:5862330-5862768	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr7:5862327-5862966	GM12878	blood:	n/a	n/a
8	ATF2	chr7:5862355-5862904	GM12878	blood:	n/a	n/a
9	ATF2	chr7:5862306-5862777	H1-hESC	embryonic stem cell:	n/a	n/a
10	ATF3	chr7:5862558-5862865	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF3	chr7:5862563-5862853	HepG2	liver:	n/a	n/a
12	ATF3	chr7:5862411-5862898	H1-hESC	embryonic stem cell:	n/a	n/a
13	ATF3	chr7:5862384-5862926	GM12878	blood:	n/a	n/a
14	ATF3	chr7:5862540-5862867	K562	blood:	n/a	n/a
15	ATF3	chr7:5862421-5862902	HepG2	liver:	n/a	n/a
16	ATF3	chr7:5862635-5862799	GM12878	blood:	n/a	n/a
17	BATF	chr7:5896136-5896348	GM12878	blood:	n/a	n/a
18	BCLAF1	chr7:5896165-5896407	GM12878	blood:	n/a	n/a
19	BCLAF1	chr7:5862267-5862957	GM12878	blood:	n/a	n/a
20	BHLHE40	chr7:5862309-5862995	GM12878	blood:	n/a	n/a
21	BHLHE40	chr7:5862470-5862879	HepG2	liver:	n/a	n/a
22	BHLHE40	chr7:5889190-5889204	K562	blood:	n/a	n/a
23	BHLHE40	chr7:5896140-5896326	GM12878	blood:	n/a	n/a
24	BHLHE40	chr7:5862350-5862941	K562	blood:	n/a	n/a
25	BRCA1	chr7:5896176-5896337	Hela-S3	cervix:	n/a	n/a
26	BRCA1	chr7:5862392-5862880	Hela-S3	cervix:	n/a	n/a
27	CBX3	chr7:5862294-5862858	K562	blood:	n/a	n/a
28	CBX3	chr7:5862122-5862937	K562	blood:	n/a	n/a
29	CCNT2	chr7:5862562-5862965	K562	blood:	n/a	n/a
30	CEBPB	chr7:5893018-5893091	Hela-S3	cervix:	n/a	chr7:5893027-5893038
31	CEBPB	chr7:5862485-5862785	H1-hESC	embryonic stem cell:	n/a	n/a
32	CEBPB	chr7:5862485-5862789	HepG2	liver:	n/a	n/a
33	CEBPB	chr7:5890535-5890604	H1-hESC	embryonic stem cell:	n/a	chr7:5890571-5890582
34	CEBPB	chr7:5857273-5857447	K562	blood:	n/a	n/a
35	CEBPB	chr7:5892955-5893172	K562	blood:	n/a	chr7:5893027-5893038
36	CEBPB	chr7:5862300-5862905	Hela-S3	cervix:	n/a	n/a
37	CEBPB	chr7:5892975-5893180	HepG2	liver:	n/a	chr7:5893027-5893038
38	CEBPB	chr7:5890537-5890700	A549	lung:	n/a	chr7:5890571-5890582
39	CEBPB	chr7:5891846-5891857	H1-hESC	embryonic stem cell:	n/a	n/a
40	CEBPB	chr7:5891809-5891870	IMR90	lung:	n/a	n/a
41	CEBPB	chr7:5890492-5890732	K562	blood:	n/a	chr7:5890571-5890582
42	CEBPB	chr7:5892977-5893179	IMR90	lung:	n/a	chr7:5893027-5893038
43	CEBPB	chr7:5890460-5890688	HepG2	liver:	n/a	chr7:5890571-5890582
44	CEBPB	chr7:5872011-5872190	K562	blood:	n/a	n/a
45	CEBPB	chr7:5896180-5896389	Hela-S3	cervix:	n/a	n/a
46	CEBPB	chr7:5892913-5893127	H1-hESC	embryonic stem cell:	n/a	chr7:5893027-5893038
47	CEBPB	chr7:5872758-5872976	Hela-S3	cervix:	n/a	n/a
48	CEBPB	chr7:5892975-5893174	A549	lung:	n/a	chr7:5893027-5893038
49	CEBPB	chr7:5862463-5862811	K562	blood:	n/a	n/a
50	CEBPB	chr7:5890537-5890656	IMR90	lung:	n/a	chr7:5890571-5890582

(count:1221 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:5862996-5863046	HIPEpiC	eye:	n/a
2	chr7:5862996-5863046	HIPEpiC	eye:	n/a
3	chr7:5865915-5865965	Caco-2	colon:	n/a
4	chr7:5862839-5862889	MCF-7	breast:	n/a
5	chr7:5888077-5888127	BE2_C	brain:	n/a
6	chr7:5862451-5862501	NHDF-neo	bronchial:	n/a
7	chr7:5862996-5863046	HAEpiC	amniotic membrane:	n/a
8	chr7:5862449-5862499	AG10803	skin:	n/a
9	chr7:5865915-5865965	HL-60	blood:	n/a
10	chr7:5862658-5862708	GM06990	blood:	n/a
11	chr7:5886722-5886772	HRPEpiC	eye:	n/a
12	chr7:5862609-5862659	HPAEpiC	pulmonary alveolar:	n/a
13	chr7:5863510-5863560	Jurkat	blood:	n/a
14	chr7:5859245-5859295	HepG2	liver:	n/a
15	chr7:5862449-5862499	MCF10A-Er-Src	breast:	n/a
16	chr7:5888077-5888127	SK-N-SH	brain:	n/a
17	chr7:5890037-5890087	BE2_C	brain:	n/a
18	chr7:5862661-5862711	SAEC	small airway:	n/a
19	chr7:5886722-5886772	AG10803	skin:	n/a
20	chr7:5885244-5885294	K562	blood:	n/a
21	chr7:5862449-5862499	Hela-S3	cervix:	n/a
22	chr7:5865915-5865965	SK-N-SH_RA	brain:	n/a
23	chr7:5862839-5862889	AG04450	lung:	fetal
24	chr7:5890037-5890087	CMK	blood:	n/a
25	chr7:5887023-5887073	T-47D	breast:	n/a
26	chr7:5862661-5862711	BJ	skin:	n/a
27	chr7:5887023-5887073	NT2-D1	testis:	n/a
28	chr7:5886722-5886772	Jurkat	blood:	n/a
29	chr7:5865915-5865965	HPAEpiC	pulmonary alveolar:	n/a
30	chr7:5863813-5863863	HPAEpiC	pulmonary alveolar:	n/a
31	chr7:5888077-5888127	HNPCEpiC	eye:	n/a
32	chr7:5865915-5865965	BJ	skin:	n/a
33	chr7:5862449-5862499	Caco-2	colon:	n/a
34	chr7:5862740-5862790	SK-N-SH_RA	brain:	n/a
35	chr7:5862996-5863046	SK-N-SH	brain:	n/a
36	chr7:5887023-5887073	SK-N-SH	brain:	n/a
37	chr7:5890037-5890087	Hepatocyte	liver:	n/a
38	chr7:5862839-5862889	NHBE	bronchial:	n/a
39	chr7:5859245-5859295	ECC-1	luminal epithelium:	n/a
40	chr7:5862839-5862889	PANC-1	pancreas:	n/a
41	chr7:5862740-5862790	U87	brain:	n/a
42	chr7:5865915-5865965	SK-N-MC	brain:	n/a
43	chr7:5862609-5862659	HNPCEpiC	eye:	n/a
44	chr7:5887023-5887073	HMEC	breast:	n/a
45	chr7:5863813-5863863	AG04450	lung:	fetal
46	chr7:5863510-5863560	GM19239	blood:	n/a
47	chr7:5865915-5865965	SK-N-SH	brain:	n/a
48	chr7:5883645-5883695	SK-N-SH	brain:	n/a
49	chr7:5887023-5887073	H1-hESC	embryonic stem cell:	embryo
50	chr7:5885244-5885294	ovcar-3	ovarian:	n/a

(count:13 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:5464152..5466960-chr7:5862123..5864390,2	MCF-7	breast:
2	chr7:5895754..5896691-chr7:6036473..6037181,2	MCF-7	breast:
3	chr7:5866466..5869217-chr7:5871734..5873608,2	MCF-7	breast:
4	chr7:5877107..5878733-chr7:5880762..5883645,2	K562	blood:
5	chr7:5875724..5878623-chr7:5880700..5882793,2	MCF-7	breast:
6	chr7:5198471..5200829-chr7:5846767..5848341,2	MCF-7	breast:
7	chr7:5866466..5869217-chr7:5871734..5873608,2	MCF-7	breast:
8	chr7:5877192..5879014-chr7:6172405..6175361,2	K562	blood:
9	chr7:5877107..5878733-chr7:5880762..5883645,2	K562	blood:
10	chr7:5896217..5898583-chr7:97641356..97642858,2	MCF-7	breast:
11	chr3:107149613..107150322-chr7:5862636..5863385,2	NB4	blood:
12	chr7:5195253..5196797-chr7:5849975..5851503,2	MCF-7	breast:
13	chr7:5875724..5878623-chr7:5880700..5882793,2	MCF-7	breast:

(count:16 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-OCM-3	chr7:5873158-5873199	NONHSAT118948
2	lnc-OCM-1	chr7:5855829-5855979	XLOC_005976
3	lnc-OCM-3	chr7:5878820-5878850	NONHSAT118948
4	lnc-OCM-1	chr7:5850593-5850617	NONHSAT118937
5	lnc-OCM-3	chr7:5873158-5873199	NONHSAT118944
6	lnc-OCM-1	chr7:5855828-5855979	NONHSAT118937
7	lnc-OCM-3	chr7:5873158-5873199	NONHSAT118942
8	lnc-OCM-3	chr7:5879580-5879706	NONHSAT118944
9	lnc-OCM-3	chr7:5878701-5878783	NONHSAT118942
10	lnc-OCM-3	chr7:5893738-5893857	NONHSAT118944
11	lnc-OCM-1	chr7:5850594-5850617	XLOC_005976
12	lnc-OCM-3	chr7:5880321-5880487	NONHSAT118944
13	lnc-OCM-3	chr7:5862875-5863157	NONHSAT118948
14	lnc-OCM-3	chr7:5862820-5863157	NONHSAT118942
15	lnc-OCM-3	chr7:5862823-5863157	NONHSAT118944
16	lnc-OCM-3	chr7:5870812-5870914	NONHSAT118942

No data

Variant related genes	Relation type
ZNF815P	TF binding region
ZNF815P	CpG island
ENSG00000273125	chromatin interactions
ENSG00000182095	chromatin interactions
ENSG00000272953	chromatin interactions
NR3C1	miRNA target sites

Extended variants
information (count: 3943 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:3943 , 50 per page) page: 1 2 3 4 5 6 7 ... 79

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12375116	chr7:5843430-5843431	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs377107445	chr7:5843431-5843432	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs537563462	chr7:5843443-5843444	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs559588897	chr7:5843454-5843455	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs551105771	chr7:5843466-5843467	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs376879323	chr7:5843473-5843474	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs141888232	chr7:5843474-5843475	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs369056086	chr7:5843486-5843487	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs147032466	chr7:5843498-5843499	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs549439825	chr7:5843525-5843526	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs536488152	chr7:5843539-5843540	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs567578051	chr7:5843554-5843555	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs56351202	chr7:5843573-5843574	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs546640420	chr7:5843641-5843642	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs62455910	chr7:5843647-5843648	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs533918218	chr7:5843657-5843658	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs370364885	chr7:5843675-5843676	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs143264992	chr7:5843724-5843725	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs376419312	chr7:5843735-5843736	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs575892683	chr7:5843748-5843749	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs148327370	chr7:5843761-5843762	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs547478787	chr7:5843789-5843790	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs573595786	chr7:5843798-5843799	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs541031244	chr7:5843800-5843801	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs113827118	chr7:5843808-5843809	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs577538101	chr7:5843809-5843810	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs544384341	chr7:5843818-5843819	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs11971558	chr7:5843843-5843844	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs563176442	chr7:5843848-5843849	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs530594737	chr7:5843849-5843850	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs142695953	chr7:5843868-5843869	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs561445089	chr7:5843872-5843873	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs146034377	chr7:5843880-5843881	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs184785974	chr7:5843903-5843904	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs571637111	chr7:5843915-5843916	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs189126167	chr7:5843923-5843924	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs551275432	chr7:5843930-5843931	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs540180812	chr7:5843935-5843936	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs569519933	chr7:5843942-5843943	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs542095393	chr7:5843949-5843950	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs536843513	chr7:5843953-5843954	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs558171152	chr7:5843969-5843970	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs554823018	chr7:5843978-5843979	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs567358415	chr7:5843987-5843988	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs139446553	chr7:5843988-5843989	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs573150367	chr7:5844021-5844022	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs552564472	chr7:5844032-5844033	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs538537282	chr7:5844037-5844038	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs544928750	chr7:5844090-5844091	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs556831475	chr7:5844127-5844128	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:82)

Disease	PMID	Source
Lynch syndrome	22585707	CNVD
Follicular lymphoma	20505157	CNVD
Breast cancer	16397240	CNVD
Raine Syndrome	17924334	CNVD
Diffuse large b-cell lymphoma	21266526	CNVD
Melanoma	18172304	CNVD
Sudden cardiac death	19188705	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	CNVD
Glioma	18556773	CNVD
Ovarian cancer	21720365	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Ovarian cancer	22174824	CNVD
Urothelial carcinoma	18382360	CNVD
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Biliary cancer	19435499	CNVD
Cancer	16751803	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Wilms tumour	21544195	CNVD
Glioblastoma multiforme	17387387	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	18923191	CNVD
Glioma	21971842	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Oral cancer	21386901	CNVD
colon cancer	17210682	CNVD
Lung adenocarcinoma	21810691	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Colorectal cancer	19359472	CNVD
Hypothalamic hamartomas	18252217	CNVD
Human rectal carcinomas	16397240	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Medulloblastoma	18056178	CNVD
Basal cell lymphoma	17170743	CNVD
Ewing''s sarcoma	21437220	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Developmental delay	21147756	CNVD
Prostate cancer	18632612	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Leukemia	23979775	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Urothelial carcinoma	21177765	CNVD
Bladder cancer	21909424	CNVD
Myelofibrosis	22110671	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	21045282	CNVD
Disorders of sex development	21048976	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Schizophrenia	21346763	CNVD
Acute myeloid leukemia	21251322	CNVD
Pancreatic cancer	17952125	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD

Chromatin state (count:867 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:5841400-5849800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr7:5842400-5843600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr7:5843000-5844200	Enhancers	Cortex derived primary cultured neurospheres	brain
4	chr7:5843200-5843600	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr7:5843600-5844200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr7:5843600-5844600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr7:5844800-5845000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr7:5847800-5848200	Enhancers	HepG2	liver
9	chr7:5848200-5849200	Weak transcription	HepG2	liver
10	chr7:5849200-5850000	Enhancers	HepG2	liver
11	chr7:5849600-5850600	Enhancers	Brain Germinal Matrix	brain
12	chr7:5849800-5851200	Enhancers	Fetal Brain Male	brain
13	chr7:5850200-5850400	Enhancers	K562	blood
14	chr7:5850200-5851400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr7:5850400-5851000	Weak transcription	K562	blood
16	chr7:5850400-5851200	Enhancers	Cortex derived primary cultured neurospheres	brain
17	chr7:5850600-5851000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
18	chr7:5851000-5851600	Enhancers	K562	blood
19	chr7:5858200-5862000	Weak transcription	K562	blood
20	chr7:5859400-5860000	Enhancers	Primary neutrophils fromperipheralblood	blood
21	chr7:5859400-5860200	Enhancers	Primary hematopoietic stem cells	blood
22	chr7:5859400-5861400	Enhancers	HUVEC	blood vessel
23	chr7:5859600-5860000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr7:5859600-5860000	Enhancers	Monocytes-CD14+_RO01746	blood
25	chr7:5859600-5860800	Enhancers	Primary hematopoietic stem cells short term culture	blood
26	chr7:5859600-5862200	Enhancers	Primary monocytes fromperipheralblood	blood
27	chr7:5859800-5861200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
28	chr7:5860000-5860200	Enhancers	Primary B cells from cord blood	blood
29	chr7:5860000-5860200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chr7:5860000-5860200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
31	chr7:5860000-5861200	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
32	chr7:5860200-5860400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
33	chr7:5860200-5860600	Active TSS	Monocytes-CD14+_RO01746	blood
34	chr7:5860200-5862000	Weak transcription	Primary hematopoietic stem cells	blood
35	chr7:5860400-5860600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr7:5860600-5860800	Enhancers	Fetal Muscle Trunk	muscle
37	chr7:5860600-5861000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
38	chr7:5860600-5861000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
39	chr7:5860800-5861000	Enhancers	Primary B cells from peripheral blood	blood
40	chr7:5860800-5861000	Enhancers	Fetal Thymus	thymus
41	chr7:5860800-5862000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
42	chr7:5861000-5861400	Enhancers	Monocytes-CD14+_RO01746	blood
43	chr7:5861000-5862000	Weak transcription	Primary B cells from peripheral blood	blood
44	chr7:5861000-5862000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
45	chr7:5861000-5862000	Weak transcription	Fetal Muscle Trunk	muscle
46	chr7:5861000-5862000	Weak transcription	Fetal Thymus	thymus
47	chr7:5861200-5861600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
48	chr7:5861200-5862000	Enhancers	Primary neutrophils fromperipheralblood	blood
49	chr7:5861400-5861800	Weak transcription	HUVEC	blood vessel
50	chr7:5861400-5861800	Weak transcription	Monocytes-CD14+_RO01746	blood

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