Variant report

Variant	nsv887423
Chromosome Location	chr7:5826501-5919280
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1377)
CpG islands
(count:1834)
Chromatin interactive
region (count:13)
LncRNA
region (count:20)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1377 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:5862528-5862814	K562	blood:	n/a	n/a
2	ARID3A	chr7:5867459-5867694	K562	blood:	n/a	n/a
3	ARID3A	chr7:5826122-5826510	K562	blood:	n/a	n/a
4	ARID3A	chr7:5862273-5862605	HepG2	liver:	n/a	n/a
5	ARID3A	chr7:5837477-5837688	K562	blood:	n/a	n/a
6	ARID3A	chr7:5867592-5867694	HepG2	liver:	n/a	n/a
7	ARID3A	chr7:5908686-5908892	HepG2	liver:	n/a	n/a
8	ATF1	chr7:5837427-5837729	K562	blood:	n/a	n/a
9	ATF1	chr7:5862457-5862892	K562	blood:	n/a	n/a
10	ATF2	chr7:5862306-5862777	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF2	chr7:5862327-5862966	GM12878	blood:	n/a	n/a
12	ATF2	chr7:5862330-5862768	H1-hESC	embryonic stem cell:	n/a	n/a
13	ATF2	chr7:5862355-5862904	GM12878	blood:	n/a	n/a
14	ATF3	chr7:5862563-5862853	HepG2	liver:	n/a	n/a
15	ATF3	chr7:5862558-5862865	H1-hESC	embryonic stem cell:	n/a	n/a
16	ATF3	chr7:5862635-5862799	GM12878	blood:	n/a	n/a
17	ATF3	chr7:5862540-5862867	K562	blood:	n/a	n/a
18	ATF3	chr7:5862384-5862926	GM12878	blood:	n/a	n/a
19	ATF3	chr7:5862411-5862898	H1-hESC	embryonic stem cell:	n/a	n/a
20	ATF3	chr7:5862421-5862902	HepG2	liver:	n/a	n/a
21	BATF	chr7:5896136-5896348	GM12878	blood:	n/a	n/a
22	BCLAF1	chr7:5896165-5896407	GM12878	blood:	n/a	n/a
23	BCLAF1	chr7:5862267-5862957	GM12878	blood:	n/a	n/a
24	BHLHE40	chr7:5830403-5830547	A549	lung:	n/a	n/a
25	BHLHE40	chr7:5862350-5862941	K562	blood:	n/a	n/a
26	BHLHE40	chr7:5896140-5896326	GM12878	blood:	n/a	n/a
27	BHLHE40	chr7:5862470-5862879	HepG2	liver:	n/a	n/a
28	BHLHE40	chr7:5889190-5889204	K562	blood:	n/a	n/a
29	BHLHE40	chr7:5862309-5862995	GM12878	blood:	n/a	n/a
30	BRCA1	chr7:5862392-5862880	Hela-S3	cervix:	n/a	n/a
31	BRCA1	chr7:5896176-5896337	Hela-S3	cervix:	n/a	n/a
32	CBX3	chr7:5825939-5826501	K562	blood:	n/a	n/a
33	CBX3	chr7:5862122-5862937	K562	blood:	n/a	n/a
34	CBX3	chr7:5862294-5862858	K562	blood:	n/a	n/a
35	CCNT2	chr7:5862562-5862965	K562	blood:	n/a	n/a
36	CEBPB	chr7:5891809-5891870	IMR90	lung:	n/a	n/a
37	CEBPB	chr7:5872758-5872976	Hela-S3	cervix:	n/a	n/a
38	CEBPB	chr7:5893018-5893091	Hela-S3	cervix:	n/a	chr7:5893027-5893038
39	CEBPB	chr7:5891846-5891857	H1-hESC	embryonic stem cell:	n/a	n/a
40	CEBPB	chr7:5912087-5912368	IMR90	lung:	n/a	n/a
41	CEBPB	chr7:5890460-5890688	HepG2	liver:	n/a	chr7:5890571-5890582
42	CEBPB	chr7:5892975-5893174	A549	lung:	n/a	chr7:5893027-5893038
43	CEBPB	chr7:5862463-5862811	K562	blood:	n/a	n/a
44	CEBPB	chr7:5862300-5862905	Hela-S3	cervix:	n/a	n/a
45	CEBPB	chr7:5890537-5890656	IMR90	lung:	n/a	chr7:5890571-5890582
46	CEBPB	chr7:5862485-5862789	HepG2	liver:	n/a	n/a
47	CEBPB	chr7:5892977-5893179	IMR90	lung:	n/a	chr7:5893027-5893038
48	CEBPB	chr7:5890492-5890732	K562	blood:	n/a	chr7:5890571-5890582
49	CEBPB	chr7:5862485-5862785	H1-hESC	embryonic stem cell:	n/a	n/a
50	CEBPB	chr7:5857273-5857447	K562	blood:	n/a	n/a

(count:1834 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:5862449-5862499	H1-hESC	embryonic stem cell:	embryo
2	chr7:5862451-5862501	PFSK-1	brain:	n/a
3	chr7:5862983-5863033	GM06990	blood:	n/a
4	chr7:5834292-5834342	SK-N-SH_RA	brain:	n/a
5	chr7:5862449-5862499	H1-hESC	embryonic stem cell:	embryo
6	chr7:5862451-5862501	PFSK-1	brain:	n/a
7	chr7:5862983-5863033	GM06990	blood:	n/a
8	chr7:5834292-5834342	SK-N-SH_RA	brain:	n/a
9	chr7:5862609-5862659	SK-N-SH_RA	brain:	n/a
10	chr7:5863813-5863863	NH-A	brain:	n/a
11	chr7:5862609-5862659	AG10803	skin:	n/a
12	chr7:5862661-5862711	T-47D	breast:	n/a
13	chr7:5833275-5833325	CMK	blood:	n/a
14	chr7:5887023-5887073	HCF	heart:	n/a
15	chr7:5886722-5886772	AG09319	gingival:	n/a
16	chr7:5888077-5888127	HRE	kidney:	n/a
17	chr7:5888077-5888127	SKMC	muscle:	n/a
18	chr7:5911900-5911950	HL-60	blood:	n/a
19	chr7:5834425-5834475	HAEpiC	amniotic membrane:	n/a
20	chr7:5862983-5863033	BJ	skin:	n/a
21	chr7:5862661-5862711	NB4	blood:	n/a
22	chr7:5863813-5863863	AoSMC	blood vessel:	n/a
23	chr7:5862996-5863046	SK-N-SH_RA	brain:	n/a
24	chr7:5862996-5863046	HUVEC	blood vessel:	n/a
25	chr7:5862983-5863033	HCF	heart:	n/a
26	chr7:5886722-5886772	K562	blood:	n/a
27	chr7:5883645-5883695	HAEpiC	amniotic membrane:	n/a
28	chr7:5862839-5862889	HCF	heart:	n/a
29	chr7:5833383-5833433	ovcar-3	ovarian:	n/a
30	chr7:5833383-5833433	H1-hESC	embryonic stem cell:	embryo
31	chr7:5911701-5911751	AG09319	gingival:	n/a
32	chr7:5888077-5888127	HL-60	blood:	n/a
33	chr7:5862996-5863046	AG09309	skin:	n/a
34	chr7:5862740-5862790	NH-A	brain:	n/a
35	chr7:5865915-5865965	AG09319	gingival:	n/a
36	chr7:5863510-5863560	HPAEpiC	pulmonary alveolar:	n/a
37	chr7:5834425-5834475	K562	blood:	n/a
38	chr7:5859245-5859295	HEEpiC	esophagus:	n/a
39	chr7:5919012-5919062	GM12892	blood:	n/a
40	chr7:5911900-5911950	HIPEpiC	eye:	n/a
41	chr7:5833275-5833325	NHBE	bronchial:	n/a
42	chr7:5859245-5859295	H1-hESC	embryonic stem cell:	embryo
43	chr7:5911900-5911950	A549	lung:	n/a
44	chr7:5862658-5862708	SK-N-MC	brain:	n/a
45	chr7:5911900-5911950	BJ	skin:	n/a
46	chr7:5911800-5911850	MCF10A-Er-Src	breast:	n/a
47	chr7:5863510-5863560	HepG2	liver:	n/a
48	chr7:5862983-5863033	MCF10A-Er-Src	breast:	n/a
49	chr7:5862983-5863033	LNCaP	prostate:	n/a
50	chr7:5885244-5885294	MCF10A-Er-Src	breast:	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	chr7:5866466..5869217-chr7:5871734..5873608,2	MCF-7	breast:
3	chr7:5875724..5878623-chr7:5880700..5882793,2	MCF-7	breast:
4	chr7:5877192..5879014-chr7:6172405..6175361,2	K562	blood:
5	chr7:5895754..5896691-chr7:6036473..6037181,2	MCF-7	breast:
6	chr7:5877107..5878733-chr7:5880762..5883645,2	K562	blood:
7	chr7:5195253..5196797-chr7:5849975..5851503,2	MCF-7	breast:
8	chr7:5866466..5869217-chr7:5871734..5873608,2	MCF-7	breast:
9	chr7:5875724..5878623-chr7:5880700..5882793,2	MCF-7	breast:
10	chr7:5198471..5200829-chr7:5846767..5848341,2	MCF-7	breast:
11	chr7:5896217..5898583-chr7:97641356..97642858,2	MCF-7	breast:
12	chr3:107149613..107150322-chr7:5862636..5863385,2	NB4	blood:
13	chr7:5877107..5878733-chr7:5880762..5883645,2	K562	blood:

(count:20 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-OCM-3	chr7:5879580-5879706	NONHSAT118944
2	lnc-OCM-1	chr7:5834113-5834518	XLOC_005976
3	lnc-OCM-3	chr7:5870812-5870914	NONHSAT118942
4	lnc-OCM-3	chr7:5862823-5863157	NONHSAT118944
5	lnc-RSPH10B-1	chr7:5911384-5911681	NONHSAT118956
6	lnc-OCM-3	chr7:5873158-5873199	NONHSAT118944
7	lnc-OCM-1	chr7:5855828-5855979	NONHSAT118937
8	lnc-OCM-1	chr7:5855829-5855979	XLOC_005976
9	lnc-OCM-1	chr7:5834112-5834518	NONHSAT118937
10	lnc-OCM-3	chr7:5880321-5880487	NONHSAT118944
11	lnc-OCM-1	chr7:5850594-5850617	XLOC_005976
12	lnc-OCM-3	chr7:5873158-5873199	NONHSAT118942
13	lnc-OCM-1	chr7:5834113-5834518	XLOC_005976
14	lnc-OCM-3	chr7:5862875-5863157	NONHSAT118948
15	lnc-OCM-3	chr7:5862820-5863157	NONHSAT118942
16	lnc-OCM-3	chr7:5873158-5873199	NONHSAT118948
17	lnc-OCM-3	chr7:5893738-5893857	NONHSAT118944
18	lnc-OCM-1	chr7:5850593-5850617	NONHSAT118937
19	lnc-OCM-3	chr7:5878701-5878783	NONHSAT118942
20	lnc-OCM-3	chr7:5878820-5878850	NONHSAT118948

No data

Variant related genes	Relation type
OCM	TF binding region
ZNF815P	TF binding region
RN7SL556P	TF binding region
OCM	CpG island
ZNF815P	CpG island
RN7SL556P	CpG island
ENSG00000272953	chromatin interactions
ENSG00000273125	chromatin interactions
ENSG00000182095	chromatin interactions
NR3C1	miRNA target sites

Extended variants
information (count: 5604 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:5604 , 50 per page) page: 1 2 3 4 5 6 7 ... 113

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs55999264	chr7:5826501-5826502	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs113025164	chr7:5826505-5826506	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs537114443	chr7:5826509-5826510	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs201093207	chr7:5826522-5826523	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs377305619	chr7:5826528-5826529	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs73343338	chr7:5826530-5826531	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs141487325	chr7:5826550-5826551	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs189154370	chr7:5826557-5826558	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs181679081	chr7:5826575-5826576	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs556170941	chr7:5826613-5826614	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs138020698	chr7:5826653-5826654	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs142579975	chr7:5826655-5826656	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs563680112	chr7:5826685-5826686	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs186691678	chr7:5826697-5826698	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs191170265	chr7:5826706-5826707	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs181055191	chr7:5826711-5826712	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs528437630	chr7:5826727-5826728	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs546979787	chr7:5826739-5826740	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs565530947	chr7:5826777-5826778	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs552842933	chr7:5826792-5826793	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs185125152	chr7:5826796-5826797	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs545142370	chr7:5826814-5826815	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs189543439	chr7:5826820-5826821	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs577542295	chr7:5826843-5826844	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs143126963	chr7:5826893-5826894	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs141833726	chr7:5826900-5826901	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs4724732	chr7:5826913-5826914	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs567274060	chr7:5826948-5826949	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs562957823	chr7:5826968-5826969	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs183365415	chr7:5826983-5826984	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs373299699	chr7:5827016-5827017	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs577867506	chr7:5827027-5827028	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs530493272	chr7:5827054-5827055	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs370514069	chr7:5827108-5827109	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs139995031	chr7:5827112-5827113	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs116800071	chr7:5827142-5827143	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs146625641	chr7:5827148-5827149	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs556899171	chr7:5827170-5827171	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs187620876	chr7:5827171-5827172	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs572908340	chr7:5827209-5827210	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs540611180	chr7:5827216-5827217	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs190625922	chr7:5827245-5827246	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs532818549	chr7:5827246-5827247	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs146192237	chr7:5827273-5827274	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs368906593	chr7:5827288-5827289	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs563090805	chr7:5827322-5827323	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs4724733	chr7:5827362-5827363	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs549109315	chr7:5827380-5827381	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs567361162	chr7:5827403-5827404	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs183330745	chr7:5827416-5827417	Weak transcription	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:974 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:5821600-5833000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr7:5826200-5826600	Enhancers	Muscle Satellite Cultured Cells	--
3	chr7:5826200-5826600	Enhancers	A549	lung
4	chr7:5826200-5826600	Flanking Active TSS	K562	blood
5	chr7:5826200-5826800	Enhancers	Hela-S3	cervix
6	chr7:5826400-5826800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr7:5826400-5826800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
8	chr7:5826600-5826800	Enhancers	K562	blood
9	chr7:5826800-5831800	Weak transcription	K562	blood
10	chr7:5830800-5831200	Enhancers	Primary neutrophils fromperipheralblood	blood
11	chr7:5831800-5832200	Enhancers	K562	blood
12	chr7:5832200-5835400	Weak transcription	K562	blood
13	chr7:5833000-5833600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr7:5833600-5836400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr7:5835200-5836000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr7:5835400-5835800	Enhancers	ES-I3 Cell Line	embryonic stem cell
17	chr7:5835400-5835800	Enhancers	HUES48 Cell Line	embryonic stem cell
18	chr7:5835400-5835800	Enhancers	iPS-20b Cell Line	embryonic stem cell
19	chr7:5835400-5836000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
20	chr7:5835400-5836200	Enhancers	HepG2	liver
21	chr7:5835400-5838000	Enhancers	K562	blood
22	chr7:5836400-5836600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
23	chr7:5836400-5837600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
24	chr7:5836400-5837800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr7:5837200-5837800	Enhancers	Primary T cells fromperipheralblood	blood
26	chr7:5837200-5838000	Enhancers	Primary hematopoietic stem cells short term culture	blood
27	chr7:5837200-5838200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
28	chr7:5837400-5837800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
29	chr7:5841400-5849800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
30	chr7:5842400-5843600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr7:5842600-5843200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
32	chr7:5843000-5844200	Enhancers	Cortex derived primary cultured neurospheres	brain
33	chr7:5843200-5843600	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
34	chr7:5843600-5844200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
35	chr7:5843600-5844600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr7:5844800-5845000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr7:5847800-5848200	Enhancers	HepG2	liver
38	chr7:5848200-5849200	Weak transcription	HepG2	liver
39	chr7:5849200-5850000	Enhancers	HepG2	liver
40	chr7:5849600-5850600	Enhancers	Brain Germinal Matrix	brain
41	chr7:5849800-5851200	Enhancers	Fetal Brain Male	brain
42	chr7:5850200-5850400	Enhancers	K562	blood
43	chr7:5850200-5851400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
44	chr7:5850400-5851000	Weak transcription	K562	blood
45	chr7:5850400-5851200	Enhancers	Cortex derived primary cultured neurospheres	brain
46	chr7:5850600-5851000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
47	chr7:5851000-5851600	Enhancers	K562	blood
48	chr7:5858200-5862000	Weak transcription	K562	blood
49	chr7:5859400-5860000	Enhancers	Primary neutrophils fromperipheralblood	blood
50	chr7:5859400-5860200	Enhancers	Primary hematopoietic stem cells	blood

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