Variant report

Variant	nsv946376
Chromosome Location	chr1:149729856-149783106
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:808)
CpG islands
(count:611)
Chromatin interactive
region (count:12)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:4)

(count:808 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:149764085-149764195	K562	blood:	n/a	n/a
2	ARID3A	chr1:149748718-149748918	K562	blood:	n/a	n/a
3	ARID3A	chr1:149747121-149747405	K562	blood:	n/a	n/a
4	ARID3A	chr1:149764146-149764192	HepG2	liver:	n/a	n/a
5	ATF1	chr1:149747159-149747411	K562	blood:	n/a	n/a
6	ATF3	chr1:149759342-149759524	K562	blood:	n/a	n/a
7	BACH1	chr1:149783062-149783253	K562	blood:	n/a	n/a
8	BATF	chr1:149783100-149783925	GM12878	blood:	n/a	n/a
9	BATF	chr1:149736086-149736381	GM12878	blood:	n/a	n/a
10	BATF	chr1:149743595-149743947	GM12878	blood:	n/a	n/a
11	BATF	chr1:149764009-149764293	GM12878	blood:	n/a	n/a
12	BATF	chr1:149743599-149744024	GM12878	blood:	n/a	n/a
13	BATF	chr1:149764414-149764725	GM12878	blood:	n/a	n/a
14	BCL11A	chr1:149743727-149744116	GM12878	blood:	n/a	chr1:149743777-149743786 chr1:149743741-149743750
15	BCL11A	chr1:149764220-149764668	GM12878	blood:	n/a	n/a
16	BCL11A	chr1:149764379-149764550	GM12878	blood:	n/a	n/a
17	BCL11A	chr1:149743550-149744000	GM12878	blood:	n/a	chr1:149743777-149743786 chr1:149743741-149743750
18	BCLAF1	chr1:149764461-149764768	GM12878	blood:	n/a	n/a
19	BHLHE40	chr1:149764150-149764212	GM12878	blood:	n/a	n/a
20	BHLHE40	chr1:149764016-149764210	HepG2	liver:	n/a	n/a
21	BHLHE40	chr1:149764585-149764716	GM12878	blood:	n/a	n/a
22	CBX3	chr1:149747108-149747994	K562	blood:	n/a	n/a
23	CBX3	chr1:149764404-149764727	K562	blood:	n/a	n/a
24	CBX3	chr1:149759046-149759963	K562	blood:	n/a	n/a
25	CBX3	chr1:149759117-149759881	K562	blood:	n/a	n/a
26	CBX3	chr1:149763933-149764334	K562	blood:	n/a	n/a
27	CEBPB	chr1:149782680-149783047	K562	blood:	n/a	n/a
28	CEBPB	chr1:149782794-149782912	H1-hESC	embryonic stem cell:	n/a	n/a
29	CEBPB	chr1:149782812-149782906	A549	lung:	n/a	n/a
30	CEBPB	chr1:149782793-149783012	Hela-S3	cervix:	n/a	n/a
31	CEBPB	chr1:149759424-149759644	Hela-S3	cervix:	n/a	n/a
32	CEBPB	chr1:149782689-149782924	K562	blood:	n/a	n/a
33	CEBPB	chr1:149782799-149783005	K562	blood:	n/a	n/a
34	CEBPB	chr1:149747238-149747477	K562	blood:	n/a	n/a
35	CEBPB	chr1:149764019-149764219	Hela-S3	cervix:	n/a	n/a
36	CEBPB	chr1:149764592-149764774	H1-hESC	embryonic stem cell:	n/a	n/a
37	CEBPB	chr1:149764150-149764237	H1-hESC	embryonic stem cell:	n/a	n/a
38	CEBPB	chr1:149759424-149759816	K562	blood:	n/a	n/a
39	CEBPB	chr1:149759308-149759875	K562	blood:	n/a	n/a
40	CEBPB	chr1:149747233-149747432	K562	blood:	n/a	n/a
41	CEBPB	chr1:149763981-149764283	K562	blood:	n/a	n/a
42	CEBPB	chr1:149759101-149760012	K562	blood:	n/a	n/a
43	CEBPB	chr1:149764492-149764695	Hela-S3	cervix:	n/a	n/a
44	CEBPD	chr1:149759241-149759973	K562	blood:	n/a	n/a
45	CHD2	chr1:149764158-149764279	Hela-S3	cervix:	n/a	n/a
46	CHD2	chr1:149764577-149764781	H1-hESC	embryonic stem cell:	n/a	n/a
47	CREB1	chr1:149764535-149764775	A549	lung:	n/a	n/a
48	CTCF	chr1:149764580-149764730	Hela-S3	cervix:	n/a	n/a
49	CTCF	chr1:149763919-149764784	A549	lung:	n/a	chr1:149764749-149764762
50	CTCF	chr1:149764120-149764270	HRE	kidney:	n/a	n/a

(count:611 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:149758962-149759012	Caco-2	colon:	n/a
2	chr1:149758962-149759012	Caco-2	colon:	n/a
3	chr1:149758962-149759012	MCF-7	breast:	n/a
4	chr1:149753023-149753073	ECC-1	luminal epithelium:	n/a
5	chr1:149764739-149764789	U87	brain:	n/a
6	chr1:149764342-149764392	HCM	heart:	n/a
7	chr1:149765026-149765076	ovcar-3	ovarian:	n/a
8	chr1:149782411-149782461	MCF10A-Er-Src	breast:	n/a
9	chr1:149764790-149764840	NHBE	bronchial:	n/a
10	chr1:149782411-149782461	NH-A	brain:	n/a
11	chr1:149764680-149764730	IMR90	lung:	fetal
12	chr1:149764790-149764840	GM12878	blood:	n/a
13	chr1:149764739-149764789	GM12892	blood:	n/a
14	chr1:149782411-149782461	PANC-1	pancreas:	n/a
15	chr1:149767909-149767959	ovcar-3	ovarian:	n/a
16	chr1:149764294-149764344	ECC-1	luminal epithelium:	n/a
17	chr1:149764790-149764840	Hela-S3	cervix:	n/a
18	chr1:149764739-149764789	Jurkat	blood:	n/a
19	chr1:149782411-149782461	AoSMC	blood vessel:	n/a
20	chr1:149764739-149764789	MCF10A-Er-Src	breast:	n/a
21	chr1:149764790-149764840	BE2_C	brain:	n/a
22	chr1:149764294-149764344	SK-N-MC	brain:	n/a
23	chr1:149764342-149764392	NT2-D1	testis:	n/a
24	chr1:149764680-149764730	ovcar-3	ovarian:	n/a
25	chr1:149782411-149782461	HRCEpiC	kidney:	n/a
26	chr1:149753023-149753073	HRPEpiC	eye:	n/a
27	chr1:149764342-149764392	U87	brain:	n/a
28	chr1:149764790-149764840	AG10803	skin:	n/a
29	chr1:149758962-149759012	AG09309	skin:	n/a
30	chr1:149764739-149764789	HEEpiC	esophagus:	n/a
31	chr1:149767909-149767959	HEK293	kidney:	embryo
32	chr1:149753023-149753073	MCF10A-Er-Src	breast:	n/a
33	chr1:149764680-149764730	GM12891	blood:	n/a
34	chr1:149764680-149764730	GM12892	blood:	n/a
35	chr1:149782411-149782461	Hepatocyte	liver:	n/a
36	chr1:149764739-149764789	NT2-D1	testis:	n/a
37	chr1:149765026-149765076	Caco-2	colon:	n/a
38	chr1:149764342-149764392	T-47D	breast:	n/a
39	chr1:149765026-149765076	HCPEpiC	choroid plexus:	n/a
40	chr1:149764680-149764730	LNCaP	prostate:	n/a
41	chr1:149758962-149759012	A549	lung:	n/a
42	chr1:149764342-149764392	ProgFib	skin:	n/a
43	chr1:149764294-149764344	Jurkat	blood:	n/a
44	chr1:149764294-149764344	AG09319	gingival:	n/a
45	chr1:149767909-149767959	HCM	heart:	n/a
46	chr1:149765026-149765076	CMK	blood:	n/a
47	chr1:149765026-149765076	HRPEpiC	eye:	n/a
48	chr1:149767909-149767959	CMK	blood:	n/a
49	chr1:149764790-149764840	GM19239	blood:	n/a
50	chr1:149765026-149765076	HCF	heart:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr1:149780184..149786348-chr1:149813638..149819174,10	MCF-7	breast:
2	chr1:149776274..149778448-chr1:149782482..149785276,2	MCF-7	breast:
3	chr1:146554326..146556624-chr1:149762818..149765682,2	K562	blood:
4	chr1:149764705..149766626-chr1:149783077..149785466,2	MCF-7	breast:
5	chr1:149782452..149784752-chr17:56707405..56709956,2	MCF-7	breast:
6	chr1:149782518..149784153-chr17:64298114..64300173,2	MCF-7	breast:
7	chr1:144532605..144534445-chr1:149782477..149783992,2	K562	blood:
8	chr1:149758293..149760951-chr1:149816252..149817928,2	K562	blood:
9	chr1:149780406..149781983-chr11:21191112..21193210,2	MCF-7	breast:
10	chr1:149780176..149786781-chr1:149856138..149862217,21	MCF-7	breast:
11	chr1:149780176..149782489-chr1:149856785..149858903,2	MCF-7	breast:
12	chr1:149777219..149780233-chr1:149783761..149786780,3	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FCGR1A-1	chr1:149769027-149769076	NONHSAT006251
2	lnc-HIST2H4A-3	chr1:149754726-149755507	NONHSAT006247
3	lnc-HIST2H4A-2	chr1:149761924-149761961	NONHSAT006250
4	lnc-HIST2H3D-2	chr1:149754433-149754816	ENSG00000242663.1
5	lnc-HIST2H3D-1	chr1:149763514-149764576	ENSG00000233030.2
6	lnc-HIST2H4A-3	chr1:149754284-149754330	NONHSAT006247
7	lnc-HIST2H3D-1	chr1:149757215-149759694	ENSG00000233030.2
8	lnc-HIST2H4A-2	chr1:149762793-149763231	NONHSAT006250
9	lnc-FCGR1A-1	chr1:149771333-149771795	NONHSAT006251

No data

(count:4 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	HIST2H2BF	hsa-miR-98-5p	chr1:149754506-149754531
2	HIST2H2BF	hsa-let-7e-5p	chr1:149754506-149754527
3	HIST2H2BF	hsa-miR-125b-5p	chr1:149754502-149754527
4	HIST2H2BF	hsa-let-7a-5p	chr1:149754506-149754527

Variant related genes	Relation type
FCGR1A	TF binding region
ENSG00000233030	TF binding region
ENSG00000226500	TF binding region
FCGR1A	CpG island
ENSG00000233030	CpG island
ENSG00000226500	CpG island
ENSG00000183558	chromatin interactions
ENSG00000201699	chromatin interactions
ENSG00000230832	chromatin interactions
ENSG00000254816	chromatin interactions
ENSG00000242663	chromatin interactions
ENSG00000184678	chromatin interactions
ENSG00000183598	chromatin interactions
ENSG00000272993	chromatin interactions
ENSG00000154229	chromatin interactions
ENSG00000184270	chromatin interactions
ENSG00000212195	chromatin interactions
ENSG00000184260	chromatin interactions
ENSG00000203814	chromatin interactions
ENSG00000220323	chromatin interactions
ENSG00000178096	chromatin interactions

Extended variants
information (count: 1607 )
Associated
traits (count: 114 )

Variant overlapped rSNPs/rCNVs (count:1607 , 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	rs587718762	chr1:149729859-149729860	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs587593872	chr1:149729868-149729869	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs587672299	chr1:149729878-149729879	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs587725388	chr1:149729913-149729914	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs587623145	chr1:149729952-149729953	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs373246586	chr1:149729957-149729958	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs587768148	chr1:149729974-149729975	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs587623664	chr1:149729995-149729996	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs587670099	chr1:149730061-149730062	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs587735083	chr1:149730064-149730065	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs587623025	chr1:149730074-149730075	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs376684092	chr1:149730085-149730086	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs587687977	chr1:149730090-149730091	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs587755651	chr1:149730097-149730098	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs587630399	chr1:149730106-149730107	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs587685621	chr1:149730109-149730110	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs587759040	chr1:149730124-149730125	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs2664753	chr1:149730125-149730126	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs587638107	chr1:149730139-149730140	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs112670984	chr1:149730140-149730141	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs587749546	chr1:149730141-149730142	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs7366059	chr1:149730145-149730146	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs587668917	chr1:149730148-149730149	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs200682122	chr1:149730165-149730166	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs1450639	chr1:149730167-149730168	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs587633403	chr1:149730181-149730182	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs587686900	chr1:149730203-149730204	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs587723246	chr1:149730286-149730287	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs587598346	chr1:149730287-149730288	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs587676241	chr1:149730290-149730291	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs587727894	chr1:149730302-149730303	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs7367312	chr1:149730311-149730312	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs2791013	chr1:149730357-149730358	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs373775071	chr1:149730376-149730377	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs11204877	chr1:149730422-149730423	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs7367317	chr1:149730436-149730437	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs12240200	chr1:149730437-149730438	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs2791014	chr1:149730521-149730522	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs587630229	chr1:149730549-149730550	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs71228834	chr1:149730561-149730562	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs7543949	chr1:149730578-149730579	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs587675334	chr1:149730617-149730618	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs587732701	chr1:149730620-149730621	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs587628291	chr1:149730621-149730622	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs587685688	chr1:149730783-149730784	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs587761378	chr1:149730797-149730798	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs12569080	chr1:149730834-149730835	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs200754296	chr1:149730836-149730837	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs4430374	chr1:149730860-149730861	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs587610076	chr1:149730863-149730864	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:114)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Cancer	21129771	CNVD
Non-small cell lung cancer	21385341	CNVD
Autosomal dominant nocturnal frontal lobe epilepsy	18472482	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thrombocytopenia-absent radius syndrome	21933853	CNVD
Psychiatric disorder	22848183	CNVD
Ewing''s sarcoma	21437220	CNVD
Liposarcoma	21253554	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Breast cancer	20409316	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	21183584	CNVD
Multiple myeloma	16461302	CNVD
Lung cancer	18438408	CNVD
Rett syndrome	21593744	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Systemic lupus erythematosus	21956041	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Non-small cell lung cancer	21829676	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Neuroblastoma	21899760	CNVD
Breast cancer	17899364	CNVD
Bladder cancer	19088036	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21611746	CNVD
Retinoblastoma	19183342	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Ewing''s sarcoma	17952124	CNVD
Osteosarcoma	19286668	CNVD
Osteosarcoma	17242211	CNVD
Ovarian cancer	17242211	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Schizophrenia	18990708	CNVD
Sudden cardiac death	19188705	CNVD
Plasma-cell dyscrasia	16705089	CNVD
Myeloma	17024118	CNVD
Cancer	17060936	CNVD
Multiple myeloma	16616336	CNVD
Type 2 diabetes	19141583	CNVD
Chordoma	18071362	CNVD
Hepatocellular carcinoma	18803288	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Urothelial carcinoma	21177765	CNVD
Burkitt''s lymphoma	19759907	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Follicular lymphoma	18703704	CNVD
Breast cancer	21509527	CNVD
Bladder cancer	21909424	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Liver carcinoma	19366792	CNVD
Testicular germ cell tumor	18059402	CNVD
Trisomy 5 syndrome	21098271	CNVD
Cancer	23975201	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:521 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:149725600-149731600	Weak transcription	Monocytes-CD14+_RO01746	blood
2	chr1:149727800-149738200	Weak transcription	Pancreas	Pancrea
3	chr1:149731600-149732200	Enhancers	Monocytes-CD14+_RO01746	blood
4	chr1:149732200-149734600	Weak transcription	Monocytes-CD14+_RO01746	blood
5	chr1:149734000-149735400	Enhancers	Dnd41	blood
6	chr1:149734600-149735000	Enhancers	Monocytes-CD14+_RO01746	blood
7	chr1:149734600-149735400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr1:149735000-149736200	Weak transcription	Monocytes-CD14+_RO01746	blood
9	chr1:149735200-149736600	Enhancers	Primary monocytes fromperipheralblood	blood
10	chr1:149735200-149736600	Enhancers	Primary hematopoietic stem cells short term culture	blood
11	chr1:149735400-149735800	Weak transcription	Dnd41	blood
12	chr1:149735400-149740400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
13	chr1:149735800-149738400	Enhancers	Dnd41	blood
14	chr1:149736000-149736600	Enhancers	Primary neutrophils fromperipheralblood	blood
15	chr1:149736200-149736600	Enhancers	Primary hematopoietic stem cells	blood
16	chr1:149736200-149736600	Enhancers	Monocytes-CD14+_RO01746	blood
17	chr1:149736600-149737600	Weak transcription	Monocytes-CD14+_RO01746	blood
18	chr1:149736600-149738000	Weak transcription	Primary monocytes fromperipheralblood	blood
19	chr1:149736600-149738000	Weak transcription	Primary neutrophils fromperipheralblood	blood
20	chr1:149736600-149738000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
21	chr1:149736600-149740600	Weak transcription	Primary hematopoietic stem cells	blood
22	chr1:149737600-149737800	Enhancers	Monocytes-CD14+_RO01746	blood
23	chr1:149737800-149738200	Weak transcription	Monocytes-CD14+_RO01746	blood
24	chr1:149738000-149738400	Enhancers	Primary monocytes fromperipheralblood	blood
25	chr1:149738000-149738400	Enhancers	Primary neutrophils fromperipheralblood	blood
26	chr1:149738000-149738400	Enhancers	Primary hematopoietic stem cells short term culture	blood
27	chr1:149738200-149738400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
28	chr1:149738200-149738400	Enhancers	Pancreas	Pancrea
29	chr1:149738200-149738400	Enhancers	Monocytes-CD14+_RO01746	blood
30	chr1:149738400-149739800	Weak transcription	Primary monocytes fromperipheralblood	blood
31	chr1:149738400-149740200	Weak transcription	Monocytes-CD14+_RO01746	blood
32	chr1:149738400-149740400	Weak transcription	Primary neutrophils fromperipheralblood	blood
33	chr1:149738400-149740400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
34	chr1:149738400-149740400	Weak transcription	Dnd41	blood
35	chr1:149738400-149742000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
36	chr1:149739800-149744400	Enhancers	Primary monocytes fromperipheralblood	blood
37	chr1:149740200-149742200	Enhancers	Monocytes-CD14+_RO01746	blood
38	chr1:149740400-149742400	Enhancers	Dnd41	blood
39	chr1:149740400-149742800	Enhancers	Primary neutrophils fromperipheralblood	blood
40	chr1:149740400-149742800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
41	chr1:149740400-149742800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr1:149740600-149740800	Enhancers	Primary hematopoietic stem cells	blood
43	chr1:149740800-149741200	Weak transcription	Primary hematopoietic stem cells	blood
44	chr1:149741200-149742000	Enhancers	Primary hematopoietic stem cells	blood
45	chr1:149742000-149742400	Enhancers	ES-I3 Cell Line	embryonic stem cell
46	chr1:149742000-149742800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
47	chr1:149742000-149742800	Enhancers	Primary hematopoietic stem cells short term culture	blood
48	chr1:149742200-149742600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
49	chr1:149742200-149742800	Enhancers	K562	blood
50	chr1:149742400-149746800	Weak transcription	Dnd41	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links