Variant report

Variant	nsv464706
Chromosome Location	chr7:119514703-119612541
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:722)
CpG islands
(count:122)
Chromatin interactive
region (count:132)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:722 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:119585975-119586344	K562	blood:	n/a	n/a
2	ARID3A	chr7:119556591-119556623	K562	blood:	n/a	n/a
3	ARID3A	chr7:119545914-119546769	K562	blood:	n/a	n/a
4	ARID3A	chr7:119588383-119588467	K562	blood:	n/a	n/a
5	ARID3A	chr7:119533532-119533639	K562	blood:	n/a	n/a
6	ARID3A	chr7:119574813-119574830	K562	blood:	n/a	n/a
7	ARID3A	chr7:119583732-119584605	K562	blood:	n/a	n/a
8	ARID3A	chr7:119604894-119605665	K562	blood:	n/a	n/a
9	ARID3A	chr7:119603730-119604003	K562	blood:	n/a	n/a
10	ARID3A	chr7:119535268-119535593	K562	blood:	n/a	n/a
11	ARID3A	chr7:119575623-119575727	HepG2	liver:	n/a	n/a
12	ARID3A	chr7:119533898-119533920	K562	blood:	n/a	n/a
13	ARID3A	chr7:119571360-119572258	K562	blood:	n/a	n/a
14	ARID3A	chr7:119575491-119576056	K562	blood:	n/a	n/a
15	ARID3A	chr7:119549177-119549427	K562	blood:	n/a	n/a
16	ARID3A	chr7:119565663-119566331	K562	blood:	n/a	n/a
17	ARID3A	chr7:119547213-119547605	K562	blood:	n/a	n/a
18	ARID3A	chr7:119544471-119544634	K562	blood:	n/a	n/a
19	ATF1	chr7:119565968-119566309	K562	blood:	n/a	n/a
20	ATF1	chr7:119535148-119535329	K562	blood:	n/a	n/a
21	ATF1	chr7:119590901-119591026	K562	blood:	n/a	n/a
22	ATF1	chr7:119604972-119605649	K562	blood:	n/a	n/a
23	ATF1	chr7:119549049-119549443	K562	blood:	n/a	n/a
24	ATF1	chr7:119547275-119547621	K562	blood:	n/a	n/a
25	ATF3	chr7:119604903-119605339	K562	blood:	n/a	n/a
26	ATF3	chr7:119547664-119547998	K562	blood:	n/a	n/a
27	BACH1	chr7:119589003-119589869	K562	blood:	n/a	n/a
28	BCLAF1	chr7:119588928-119590441	K562	blood:	n/a	n/a
29	BHLHE40	chr7:119566020-119566327	K562	blood:	n/a	n/a
30	BHLHE40	chr7:119549136-119549393	K562	blood:	n/a	n/a
31	BHLHE40	chr7:119578413-119578420	K562	blood:	n/a	n/a
32	CBX3	chr7:119590471-119591130	K562	blood:	n/a	n/a
33	CBX3	chr7:119604811-119605354	K562	blood:	n/a	n/a
34	CBX3	chr7:119590477-119591189	K562	blood:	n/a	n/a
35	CBX3	chr7:119524841-119525448	K562	blood:	n/a	n/a
36	CBX3	chr7:119547161-119547689	K562	blood:	n/a	n/a
37	CBX3	chr7:119603669-119604091	K562	blood:	n/a	n/a
38	CBX3	chr7:119565918-119566414	K562	blood:	n/a	n/a
39	CBX3	chr7:119607208-119607692	K562	blood:	n/a	n/a
40	CBX3	chr7:119583855-119584516	K562	blood:	n/a	n/a
41	CBX3	chr7:119565965-119566333	K562	blood:	n/a	n/a
42	CCNT2	chr7:119547305-119548071	K562	blood:	n/a	n/a
43	CCNT2	chr7:119604745-119605609	K562	blood:	n/a	n/a
44	CCNT2	chr7:119548335-119548457	K562	blood:	n/a	n/a
45	CCNT2	chr7:119515033-119515101	K562	blood:	n/a	n/a
46	CCNT2	chr7:119546099-119546321	K562	blood:	n/a	n/a
47	CCNT2	chr7:119566020-119566328	K562	blood:	n/a	n/a
48	CEBPB	chr7:119547198-119547934	K562	blood:	n/a	n/a
49	CEBPB	chr7:119609861-119610180	IMR90	lung:	n/a	chr7:119610022-119610035 chr7:119610023-119610034
50	CEBPB	chr7:119570386-119570617	HepG2	liver:	n/a	chr7:119570493-119570504

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:119590451-119590501	HRPEpiC	eye:	n/a
2	chr7:119604878-119604928	NH-A	brain:	n/a
3	chr7:119604878-119604928	PFSK-1	brain:	n/a
4	chr7:119604878-119604928	GM12891	blood:	n/a
5	chr7:119590451-119590501	HL-60	blood:	n/a
6	chr7:119604878-119604928	ECC-1	luminal epithelium:	n/a
7	chr7:119590451-119590501	HEEpiC	esophagus:	n/a
8	chr7:119590451-119590501	SK-N-SH	brain:	n/a
9	chr7:119590451-119590501	PrEC	prostate:	n/a
10	chr7:119604878-119604928	BJ	skin:	n/a
11	chr7:119604878-119604928	HNPCEpiC	eye:	n/a
12	chr7:119604878-119604928	CMK	blood:	n/a
13	chr7:119590451-119590501	GM12878	blood:	n/a
14	chr7:119604878-119604928	NHBE	bronchial:	n/a
15	chr7:119604878-119604928	U87	brain:	n/a
16	chr7:119604878-119604928	K562	blood:	n/a
17	chr7:119590451-119590501	NHBE	bronchial:	n/a
18	chr7:119604878-119604928	HCT-116	colon:	n/a
19	chr7:119590451-119590501	IMR90	lung:	fetal
20	chr7:119604878-119604928	ProgFib	skin:	n/a
21	chr7:119590451-119590501	T-47D	breast:	n/a
22	chr7:119604878-119604928	HRE	kidney:	n/a
23	chr7:119590451-119590501	HEK293	kidney:	embryo
24	chr7:119590451-119590501	LNCaP	prostate:	n/a
25	chr7:119590451-119590501	HCT-116	colon:	n/a
26	chr7:119590451-119590501	A549	lung:	n/a
27	chr7:119590451-119590501	HCPEpiC	choroid plexus:	n/a
28	chr7:119590451-119590501	AG09319	gingival:	n/a
29	chr7:119590451-119590501	MCF10A-Er-Src	breast:	n/a
30	chr7:119604878-119604928	NT2-D1	testis:	n/a
31	chr7:119604878-119604928	BE2_C	brain:	n/a
32	chr7:119590451-119590501	H1-hESC	embryonic stem cell:	embryo
33	chr7:119604878-119604928	SK-N-SH_RA	brain:	n/a
34	chr7:119604878-119604928	HL-60	blood:	n/a
35	chr7:119604878-119604928	AG10803	skin:	n/a
36	chr7:119604878-119604928	HepG2	liver:	n/a
37	chr7:119590451-119590501	GM12892	blood:	n/a
38	chr7:119604878-119604928	HRCEpiC	kidney:	n/a
39	chr7:119604878-119604928	SK-N-SH	brain:	n/a
40	chr7:119590451-119590501	BE2_C	brain:	n/a
41	chr7:119604878-119604928	GM19239	blood:	n/a
42	chr7:119604878-119604928	NHDF-neo	bronchial:	n/a
43	chr7:119604878-119604928	SK-N-MC	brain:	n/a
44	chr7:119604878-119604928	HCM	heart:	n/a
45	chr7:119604878-119604928	AG09319	gingival:	n/a
46	chr7:119590451-119590501	SK-N-SH_RA	brain:	n/a
47	chr7:119590451-119590501	RPTEC	kidney:	n/a
48	chr7:119590451-119590501	NB4	blood:	n/a
49	chr7:119604878-119604928	A549	lung:	n/a
50	chr7:119590451-119590501	Hela-S3	cervix:	n/a

(count:132 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr7:119511194..119513890-chr7:119518810..119520879,2	K562	blood:
2	chr7:119531336..119533343-chr7:119587590..119589885,2	K562	blood:
3	chr7:119596097..119601852-chr7:119602330..119605666,5	K562	blood:
4	chr7:119578083..119580196-chr7:119586572..119589192,2	K562	blood:
5	chr7:119527012..119529074-chr7:119543165..119546062,2	K562	blood:
6	chr7:119575213..119576061-chr7:119729704..119730242,2	MCF-7	breast:
7	chr7:119544617..119547371-chr7:119688407..119692790,3	K562	blood:
8	chr7:119599851..119601809-chr7:119612155..119614686,2	K562	blood:
9	chr7:119603198..119605328-chr7:119613370..119615944,2	K562	blood:
10	chr7:119570469..119572093-chr7:119577244..119578871,2	K562	blood:
11	chr7:119570545..119573012-chr7:119573015..119575598,2	K562	blood:
12	chr7:119589512..119591360-chr7:119594151..119597360,3	K562	blood:
13	chr7:119533151..119535556-chr7:119574432..119576390,2	K562	blood:
14	chr7:119584419..119586838-chr7:119603002..119604856,2	K562	blood:
15	chr7:119551448..119554657-chr7:119557824..119560982,4	K562	blood:
16	chr7:119544987..119547805-chr7:119577391..119580001,2	K562	blood:
17	chr7:119593756..119596259-chr7:119601631..119603821,2	K562	blood:
18	chr7:119545908..119547715-chr7:119552175..119553901,2	K562	blood:
19	chr7:119594641..119599063-chr7:119599275..119601348,3	K562	blood:
20	chr7:119518704..119521067-chr7:119542364..119544620,2	K562	blood:
21	chr7:119599851..119601809-chr7:119612155..119614686,2	K562	blood:
22	chr7:119570469..119574295-chr7:119575625..119578871,3	K562	blood:
23	chr7:119544847..119547589-chr7:119588940..119593130,4	K562	blood:
24	chr7:119558634..119561152-chr7:119564174..119567043,2	K562	blood:
25	chr7:119544182..119546756-chr7:119562620..119564769,3	K562	blood:
26	chr7:119590351..119592523-chr7:119610438..119612381,2	K562	blood:
27	chr7:119516671..119518877-chr7:119519641..119522411,2	K562	blood:
28	chr7:119590351..119592523-chr7:119610438..119612381,2	K562	blood:
29	chr7:119528303..119529981-chr7:119532634..119534210,2	K562	blood:
30	chr7:119535257..119536915-chr7:119542608..119545152,2	K562	blood:
31	chr7:119570997..119574569-chr7:119582922..119586334,5	K562	blood:
32	chr7:119573958..119576750-chr7:119589483..119591512,2	K562	blood:
33	chr7:119551448..119555226-chr7:119556760..119560982,4	K562	blood:
34	chr7:119569917..119573770-chr7:119586780..119589332,3	K562	blood:
35	chr7:119584419..119586838-chr7:119603002..119604856,2	K562	blood:
36	chr7:119595929..119598016-chr7:119599722..119602227,2	K562	blood:
37	chr7:119545952..119548179-chr7:119593312..119595306,2	K562	blood:
38	chr7:119545841..119548270-chr7:119587214..119590223,3	K562	blood:
39	chr7:119573362..119575942-chr7:119596349..119600152,3	K562	blood:
40	chr7:119596097..119599917-chr7:119604166..119607181,3	K562	blood:
41	chr7:119604091..119606659-chr7:119609179..119612506,3	K562	blood:
42	chr7:119573034..119574677-chr7:119575228..119577665,3	K562	blood:
43	chr7:119513227..119515980-chr7:119542011..119544758,2	K562	blood:
44	chr7:119505448..119507945-chr7:119512222..119515197,2	K562	blood:
45	chr7:119516671..119518877-chr7:119519641..119522411,2	K562	blood:
46	chr7:119604091..119606659-chr7:119609179..119612506,3	K562	blood:
47	chr7:119541414..119544010-chr7:119583938..119585593,2	K562	blood:
48	chr7:119531336..119533343-chr7:119587590..119589885,2	K562	blood:
49	chr7:119575228..119576234-chr7:119911967..119912836,4	MCF-7	breast:
50	chr7:119527652..119529791-chr7:119534255..119537137,2	K562	blood:

(count:2 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TSPAN12-4	chr7:119547347-119547429	XLOC_006580
2	lnc-TSPAN12-4	chr7:119547347-119547429	XLOC_006580

No data

Variant related genes	Relation type
ENSG00000225546	TF binding region
ENSG00000225546	CpG island
ENSG00000225546	chromatin interactions
HOXC8	miRNA target sites

Extended variants
information (count: 2820 )
Associated
traits (count: 85 )

Variant overlapped rSNPs/rCNVs (count:2820 , 50 per page) page: 1 2 3 4 5 6 7 ... 57

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2108143	chr7:119514703-119514704	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs559134107	chr7:119514817-119514818	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs528314356	chr7:119514832-119514833	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs551149848	chr7:119514841-119514842	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs571744137	chr7:119514883-119514884	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs541613568	chr7:119514932-119514933	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs191831098	chr7:119514934-119514935	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs550974796	chr7:119514936-119514937	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs530461928	chr7:119514961-119514962	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs142483289	chr7:119515023-119515024	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs73720900	chr7:119515053-119515054	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs374584560	chr7:119515060-119515061	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs147954958	chr7:119515064-119515065	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs573575188	chr7:119515080-119515081	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs528657833	chr7:119515081-119515082	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs17142410	chr7:119515189-119515190	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs11767494	chr7:119515190-119515191	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs139489819	chr7:119515214-119515215	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs145003229	chr7:119515243-119515244	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs543125499	chr7:119515305-119515306	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs534741407	chr7:119515312-119515313	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs556934409	chr7:119515345-119515346	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs573517908	chr7:119515370-119515371	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs147593747	chr7:119515422-119515423	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs184068516	chr7:119515433-119515434	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs536644873	chr7:119515438-119515439	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs528351127	chr7:119515439-119515440	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs186789239	chr7:119515461-119515462	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs539525089	chr7:119515462-119515463	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs191591202	chr7:119515474-119515475	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs140758058	chr7:119515489-119515490	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs550756542	chr7:119515491-119515492	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs567653076	chr7:119515548-119515549	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs571322513	chr7:119515554-119515555	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs530165844	chr7:119515583-119515584	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs547008240	chr7:119515589-119515590	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs56349542	chr7:119515624-119515625	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs571855679	chr7:119515632-119515633	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs539318859	chr7:119515648-119515649	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs182621473	chr7:119515669-119515670	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs569320636	chr7:119515698-119515699	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs846447	chr7:119515705-119515706	Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs556737014	chr7:119515717-119515718	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs573390535	chr7:119515763-119515764	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs537668009	chr7:119515776-119515777	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs75159354	chr7:119515791-119515792	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs552526101	chr7:119515837-119515838	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs148875538	chr7:119515848-119515849	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs115927212	chr7:119515859-119515860	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs547584506	chr7:119515876-119515877	Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:85)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Melanoma	18172304	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Squamous cell cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	17387387	CNVD
Low-grade fibromyxoid sarcoma	0	CNVD
Oligodendroglial tumors	17285580	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21264507	CNVD
Shwachman-Diamond syndrome	22934832	CNVD
Colorectal cancer	19359472	CNVD
Cutaneous malignant melanoma	17690212	CNVD
Leukemia	17361228	CNVD
Breast cancer	16461572	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Malignant melanoma	17690212	CNVD
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Multiple myeloma	17550852	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neurodevelopmental disorder	22521361	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Metanephric adenoma	20802469	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
Myelodysplastic syndrome	21251322	CNVD
Chronic myeloid leukemia	21384125	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
lymphocytic leukemia	21291569	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16573809	CNVD
Medulloblastoma	16783165	CNVD
Biliary cancer	19435499	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Prostate cancer	23792589	CNVD
Adenocarcinoma	21044232	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Non-small cell lung cancer	19889201	CNVD
Acute myeloid leukemia	18000384	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Metastatic melanoma	18483359	CNVD
Autism	18414403	CNVD
Autism	19401682	CNVD
Autism	19546859	CNVD
Schizophrenia	19546859	CNVD
Tourette syndrome	19546859	CNVD
Melanoma	19188590	CNVD
small cell lung cancer	20016488	CNVD
Glioblastoma multiforme	22286061	CNVD
Glioblastoma multiforme	21922591	CNVD
Hepatocellular carcinoma	16785998	CNVD
Glioblastoma multiforme	18628472	CNVD
Myelofibrosis	22110671	CNVD
Renal cell carcinoma	18194544	CNVD
Schizophrenia	23813976	CNVD
early-passage human iPS cells	21368824	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:151 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:119511200-119515600	Weak transcription	K562	blood
2	chr7:119515600-119516000	Strong transcription	K562	blood
3	chr7:119516000-119517000	Weak transcription	K562	blood
4	chr7:119517000-119518000	Strong transcription	K562	blood
5	chr7:119518000-119521400	Weak transcription	K562	blood
6	chr7:119521400-119521800	Enhancers	K562	blood
7	chr7:119521800-119524800	Weak transcription	K562	blood
8	chr7:119523400-119523800	Enhancers	H9 Cell Line	embryonic stem cell
9	chr7:119523400-119523800	Enhancers	HUES48 Cell Line	embryonic stem cell
10	chr7:119525800-119526200	Enhancers	HUES6 Cell Line	embryonic stem cell
11	chr7:119526000-119526400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
12	chr7:119526000-119526400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr7:119527800-119529400	ZNF genes & repeats	K562	blood
14	chr7:119529400-119537600	Weak transcription	K562	blood
15	chr7:119535000-119535400	Active TSS	Fetal Adrenal Gland	Adrenal Gland
16	chr7:119536400-119537400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
17	chr7:119537400-119539800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
18	chr7:119537600-119538000	Strong transcription	K562	blood
19	chr7:119538000-119538600	ZNF genes & repeats	K562	blood
20	chr7:119538600-119540000	Weak transcription	K562	blood
21	chr7:119539800-119541800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
22	chr7:119539800-119541800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
23	chr7:119540000-119540400	Strong transcription	K562	blood
24	chr7:119540400-119543800	Genic enhancers	K562	blood
25	chr7:119541000-119541400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
26	chr7:119541000-119541400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
27	chr7:119541000-119541600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
28	chr7:119541000-119541800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
29	chr7:119543800-119544400	Transcr. at gene 5' and 3'	K562	blood
30	chr7:119544400-119547800	Active TSS	K562	blood
31	chr7:119547400-119548200	Enhancers	iPS-15b Cell Line	embryonic stem cell
32	chr7:119547800-119548200	Enhancers	H1 Cell Line	embryonic stem cell
33	chr7:119547800-119548600	Flanking Active TSS	K562	blood
34	chr7:119548600-119549200	Enhancers	K562	blood
35	chr7:119562600-119562800	Enhancers	K562	blood
36	chr7:119562800-119564800	Weak transcription	K562	blood
37	chr7:119564800-119565400	Genic enhancers	K562	blood
38	chr7:119565400-119565600	Enhancers	K562	blood
39	chr7:119565400-119566000	Enhancers	Fetal Brain Male	brain
40	chr7:119565600-119565800	Flanking Active TSS	K562	blood
41	chr7:119565600-119566200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
42	chr7:119565600-119566400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr7:119565600-119566400	Enhancers	iPS-18 Cell Line	embryonic stem cell
44	chr7:119565800-119566000	Active TSS	K562	blood
45	chr7:119565800-119566400	Enhancers	Fetal Lung	lung
46	chr7:119566000-119566400	Flanking Active TSS	Fetal Brain Male	brain
47	chr7:119566000-119566400	Flanking Active TSS	K562	blood
48	chr7:119566400-119567400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr7:119567400-119567600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr7:119567400-119567600	ZNF genes & repeats	Primary T helper memory cells from peripheral blood 2	blood

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