Variant report

Variant	nsv2777
Chromosome Location	chr1:149682377-149740643
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:573)
CpG islands
(count:733)
Chromatin interactive
region (count:4)
LncRNA
region (count:15)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:573 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:149684007-149684371	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:149684047-149684303	K562	blood:	n/a	n/a
3	ATF2	chr1:149683980-149684475	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr1:149683987-149684400	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF3	chr1:149711658-149712146	A549	lung:	n/a	n/a
6	ATF3	chr1:149683987-149684447	K562	blood:	n/a	n/a
7	ATF3	chr1:149683962-149684559	A549	lung:	n/a	n/a
8	ATF3	chr1:149711653-149712227	A549	lung:	n/a	n/a
9	ATF3	chr1:149684003-149684461	HCT-116	colon:	n/a	n/a
10	ATF3	chr1:149683968-149684507	A549	lung:	n/a	n/a
11	BACH1	chr1:149685097-149685104	H1-hESC	embryonic stem cell:	n/a	n/a
12	BATF	chr1:149711785-149712234	GM12878	blood:	n/a	chr1:149711949-149711958
13	BATF	chr1:149711835-149712141	GM12878	blood:	n/a	chr1:149711949-149711958
14	BATF	chr1:149683995-149684314	GM12878	blood:	n/a	n/a
15	BATF	chr1:149736086-149736381	GM12878	blood:	n/a	n/a
16	BATF	chr1:149683235-149683530	GM12878	blood:	n/a	n/a
17	BATF	chr1:149704424-149704722	GM12878	blood:	n/a	n/a
18	BCL11A	chr1:149684083-149684261	GM12878	blood:	n/a	n/a
19	BCL11A	chr1:149683993-149684216	GM12878	blood:	n/a	n/a
20	BCLAF1	chr1:149684031-149684377	GM12878	blood:	n/a	n/a
21	BDP1	chr1:149683980-149684414	K562	blood:	n/a	n/a
22	BDP1	chr1:149683979-149684415	Hela-S3	cervix:	n/a	n/a
23	BHLHE40	chr1:149684001-149684491	K562	blood:	n/a	n/a
24	BHLHE40	chr1:149683593-149683827	HepG2	liver:	n/a	n/a
25	BHLHE40	chr1:149684006-149684391	HepG2	liver:	n/a	n/a
26	BHLHE40	chr1:149683216-149683541	HepG2	liver:	n/a	n/a
27	BRCA1	chr1:149684011-149684277	Hela-S3	cervix:	n/a	n/a
28	BRF1	chr1:149684005-149684353	K562	blood:	n/a	n/a
29	BRF1	chr1:149683995-149684376	Hela-S3	cervix:	n/a	n/a
30	CBX3	chr1:149683190-149684593	K562	blood:	n/a	n/a
31	CBX3	chr1:149683807-149684547	K562	blood:	n/a	n/a
32	CBX3	chr1:149684007-149684407	HCT-116	colon:	n/a	n/a
33	CEBPB	chr1:149711816-149711897	K562	blood:	n/a	chr1:149711854-149711865
34	CEBPB	chr1:149704373-149704663	K562	blood:	n/a	n/a
35	CEBPB	chr1:149721223-149721399	Hela-S3	cervix:	n/a	chr1:149721315-149721326 chr1:149721317-149721326
36	CEBPB	chr1:149721238-149721393	K562	blood:	n/a	chr1:149721315-149721326 chr1:149721317-149721326
37	CEBPB	chr1:149711697-149712038	A549	lung:	n/a	chr1:149711854-149711865
38	CEBPB	chr1:149683158-149684349	K562	blood:	n/a	n/a
39	CEBPB	chr1:149684054-149684320	K562	blood:	n/a	n/a
40	CEBPB	chr1:149711670-149712021	K562	blood:	n/a	chr1:149711854-149711865
41	CEBPB	chr1:149711788-149712001	K562	blood:	n/a	chr1:149711854-149711865
42	CEBPB	chr1:149684006-149684421	H1-hESC	embryonic stem cell:	n/a	n/a
43	CEBPB	chr1:149711642-149712210	H1-hESC	embryonic stem cell:	n/a	chr1:149711854-149711865
44	CEBPB	chr1:149711785-149711896	HepG2	liver:	n/a	chr1:149711854-149711865
45	CEBPB	chr1:149711779-149712003	IMR90	lung:	n/a	chr1:149711854-149711865
46	CEBPD	chr1:149684023-149684514	K562	blood:	n/a	n/a
47	CHD1	chr1:149719574-149719759	H1-hESC	embryonic stem cell:	n/a	n/a
48	CHD2	chr1:149684938-149685135	H1-hESC	embryonic stem cell:	n/a	n/a
49	CHD2	chr1:149684012-149684403	H1-hESC	embryonic stem cell:	n/a	n/a
50	CHD2	chr1:149684055-149684282	K562	blood:	n/a	n/a

(count:733 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:149719461-149719511	NH-A	brain:	n/a
2	chr1:149719461-149719511	NH-A	brain:	n/a
3	chr1:149719536-149719586	Jurkat	blood:	n/a
4	chr1:149719243-149719293	HIPEpiC	eye:	n/a
5	chr1:149718651-149718701	AG09319	gingival:	n/a
6	chr1:149711854-149711904	HCM	heart:	n/a
7	chr1:149719461-149719511	HCPEpiC	choroid plexus:	n/a
8	chr1:149711854-149711904	MCF-7	breast:	n/a
9	chr1:149721664-149721714	LNCaP	prostate:	n/a
10	chr1:149718671-149718721	HRCEpiC	kidney:	n/a
11	chr1:149717620-149717670	NB4	blood:	n/a
12	chr1:149684418-149684468	HIPEpiC	eye:	n/a
13	chr1:149711854-149711904	NB4	blood:	n/a
14	chr1:149717620-149717670	PFSK-1	brain:	n/a
15	chr1:149717620-149717670	NHBE	bronchial:	n/a
16	chr1:149717620-149717670	U87	brain:	n/a
17	chr1:149684418-149684468	HUVEC	blood vessel:	n/a
18	chr1:149712057-149712107	LNCaP	prostate:	n/a
19	chr1:149721664-149721714	GM12892	blood:	n/a
20	chr1:149719536-149719586	SK-N-SH	brain:	n/a
21	chr1:149719461-149719511	AG04450	lung:	fetal
22	chr1:149718651-149718701	NHBE	bronchial:	n/a
23	chr1:149719243-149719293	K562	blood:	n/a
24	chr1:149719536-149719586	GM12878	blood:	n/a
25	chr1:149684418-149684468	H1-hESC	embryonic stem cell:	embryo
26	chr1:149719536-149719586	NB4	blood:	n/a
27	chr1:149718651-149718701	HAEpiC	amniotic membrane:	n/a
28	chr1:149684561-149684611	GM12892	blood:	n/a
29	chr1:149712057-149712107	IMR90	lung:	fetal
30	chr1:149684418-149684468	CMK	blood:	n/a
31	chr1:149718671-149718721	HepG2	liver:	n/a
32	chr1:149718671-149718721	A549	lung:	n/a
33	chr1:149712057-149712107	GM12892	blood:	n/a
34	chr1:149720577-149720627	A549	lung:	n/a
35	chr1:149718651-149718701	PFSK-1	brain:	n/a
36	chr1:149684418-149684468	BJ	skin:	n/a
37	chr1:149719536-149719586	HEEpiC	esophagus:	n/a
38	chr1:149711854-149711904	BE2_C	brain:	n/a
39	chr1:149720577-149720627	AG04449	skin:	fetal
40	chr1:149721664-149721714	GM06990	blood:	n/a
41	chr1:149718671-149718721	SK-N-SH	brain:	n/a
42	chr1:149719536-149719586	NHBE	bronchial:	n/a
43	chr1:149718671-149718721	NHBE	bronchial:	n/a
44	chr1:149720577-149720627	MCF10A-Er-Src	breast:	n/a
45	chr1:149721664-149721714	MCF10A-Er-Src	breast:	n/a
46	chr1:149718671-149718721	HIPEpiC	eye:	n/a
47	chr1:149717620-149717670	Jurkat	blood:	n/a
48	chr1:149684418-149684468	GM12892	blood:	n/a
49	chr1:149684561-149684611	HCT-116	colon:	n/a
50	chr1:149719243-149719293	HRCEpiC	kidney:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr1:149298692..149300746-chr1:149683634..149686545,2	MCF-7	breast:
2	chr1:149304628..149306966-chr1:149690305..149693086,2	MCF-7	breast:
3	chr1:149305186..149307455-chr1:149691743..149693791,2	MCF-7	breast:
4	chr1:149299280..149300172-chr1:149684615..149685511,3	MCF-7	breast:

(count:15 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-HIST2H2BF-1	chr1:149691554-149691646	ENSG00000234232.2
2	lnc-HIST2H2BF-1	chr1:149692947-149693081	ENSG00000234232
3	lnc-HIST2H2BF-1	chr1:149699922-149699958	ENSG00000234232.2
4	lnc-HIST2H2BF-1	chr1:149692947-149693081	ENSG00000234232.2
5	lnc-HIST2H2BF-1	chr1:149694461-149694633	ENSG00000234232.2
6	lnc-HIST2H2BF-1	chr1:149698419-149698683	ENSG00000234232.2
7	lnc-HIST2H2BF-3	chr1:149713129-149713281	NONHSAT006245
8	lnc-HIST2H2BF-1	chr1:149694456-149694633	ENSG00000234232.2
9	lnc-AL358813.2-4	chr1:149689368-149689854	NONHSAT006243
10	lnc-HIST2H2BF-1	chr1:149698419-149698605	ENSG00000234232
11	lnc-HIST2H2BF-3	chr1:149718450-149720133	NONHSAT006245
12	lnc-HIST2H2BF-1	chr1:149694411-149694620	ENSG00000234232.2
13	lnc-HIST2H2BF-1	chr1:149698419-149698606	ENSG00000234232.2
14	lnc-HIST2H2BF-1	chr1:149691432-149691646	ENSG00000234232
15	lnc-HIST2H2BF-1	chr1:149699768-149699819	ENSG00000234232.2

No data

Variant related genes	Relation type
ENSG00000263825	TF binding region
ENSG00000226500	TF binding region
ENSG00000234232	TF binding region
ENSG00000197844	TF binding region
ENSG00000263825	CpG island
ENSG00000226500	CpG island
ENSG00000234232	CpG island
ENSG00000197844	CpG island

Extended variants
information (count: 1908 )
Associated
traits (count: 116 )

Variant overlapped rSNPs/rCNVs (count:1908 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs58870599	chr1:149682386-149682387	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs587671640	chr1:149682471-149682472	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs28541284	chr1:149682486-149682487	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs587624649	chr1:149682541-149682542	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs587676449	chr1:149682562-149682563	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs587765270	chr1:149682583-149682584	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs145153987	chr1:149682604-149682605	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs587611858	chr1:149682635-149682636	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs587694580	chr1:149682680-149682681	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs587771711	chr1:149682693-149682694	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs587675169	chr1:149682717-149682718	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs587733590	chr1:149682747-149682748	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs587775085	chr1:149682749-149682750	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs201171850	chr1:149682754-149682755	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs587642396	chr1:149682799-149682800	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs587720070	chr1:149682849-149682850	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs146882885	chr1:149682897-149682898	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs587604455	chr1:149682900-149682901	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs587672027	chr1:149682912-149682913	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs587714367	chr1:149683021-149683022	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs587595475	chr1:149683044-149683045	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs587673332	chr1:149683049-149683050	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs113810821	chr1:149683061-149683062	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs587728475	chr1:149683064-149683065	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs587618684	chr1:149683134-149683135	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs587662878	chr1:149683211-149683212	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs202081247	chr1:149683216-149683217	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs587738275	chr1:149683237-149683238	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs140479184	chr1:149683258-149683259	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs587615895	chr1:149683310-149683311	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs587691224	chr1:149683349-149683350	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs587772658	chr1:149683362-149683363	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs375952134	chr1:149683379-149683380	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs145638662	chr1:149683407-149683408	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs587650037	chr1:149683410-149683411	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs587709018	chr1:149683434-149683435	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs148102360	chr1:149683436-149683437	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs587776039	chr1:149683462-149683463	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs587639338	chr1:149683484-149683485	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs2597694	chr1:149683544-149683545	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs587723113	chr1:149683564-149683565	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs587752900	chr1:149683567-149683568	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs587636407	chr1:149683573-149683574	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs587718427	chr1:149683631-149683632	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs587595103	chr1:149683656-149683657	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs587648821	chr1:149683663-149683664	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs587710010	chr1:149683856-149683857	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs587608869	chr1:149683887-149683888	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs587655343	chr1:149683916-149683917	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs587741374	chr1:149683944-149683945	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:116)

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
Non-syndromic sensorineural hearing loss	17122850	CNVD
Myelofibrosis	22110671	CNVD
Liver carcinoma	19366792	CNVD
Testicular germ cell tumor	18059402	CNVD
Trisomy 5 syndrome	21098271	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Pancreatic cancer	17952125	CNVD
Cancer	23975201	CNVD

Chromatin state (count:595 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:149677000-149684200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
2	chr1:149677200-149684200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
3	chr1:149677400-149683000	Weak transcription	Fetal Intestine Small	intestine
4	chr1:149680200-149684000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
5	chr1:149680200-149684000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr1:149680400-149683600	Weak transcription	K562	blood
7	chr1:149683000-149683200	Enhancers	Adipose Nuclei	Adipose
8	chr1:149683000-149683200	Enhancers	Fetal Intestine Small	intestine
9	chr1:149683000-149685400	Active TSS	iPS-20b Cell Line	embryonic stem cell
10	chr1:149683200-149684000	Weak transcription	Fetal Intestine Small	intestine
11	chr1:149683400-149684200	Weak transcription	Primary monocytes fromperipheralblood	blood
12	chr1:149683400-149685000	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr1:149683400-149685200	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr1:149683600-149684200	Active TSS	H1 Cell Line	embryonic stem cell
15	chr1:149683600-149684200	Active TSS	Fetal Thymus	thymus
16	chr1:149683600-149684400	Active TSS	Fetal Adrenal Gland	Adrenal Gland
17	chr1:149683600-149684600	Active TSS	K562	blood
18	chr1:149683600-149685000	Active TSS	H9 Cell Line	embryonic stem cell
19	chr1:149683600-149685000	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
20	chr1:149683600-149685000	Active TSS	HUES48 Cell Line	embryonic stem cell
21	chr1:149683600-149685000	Active TSS	HUES6 Cell Line	embryonic stem cell
22	chr1:149683600-149685000	Active TSS	iPS-18 Cell Line	embryonic stem cell
23	chr1:149683600-149685200	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr1:149683600-149685400	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
25	chr1:149683600-149685400	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
26	chr1:149683600-149685600	Active TSS	HUES64 Cell Line	embryonic stem cell
27	chr1:149684000-149684200	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr1:149684000-149684200	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
29	chr1:149684000-149684200	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
30	chr1:149684000-149684200	Active TSS	Primary neutrophils fromperipheralblood	blood
31	chr1:149684000-149684200	Active TSS	Primary B cells from cord blood	blood
32	chr1:149684000-149684200	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
33	chr1:149684000-149684200	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
34	chr1:149684000-149684200	Bivalent/Poised TSS	Cortex derived primary cultured neurospheres	brain
35	chr1:149684000-149684200	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
36	chr1:149684000-149684200	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
37	chr1:149684000-149684200	Active TSS	Fetal Intestine Small	intestine
38	chr1:149684000-149684200	Bivalent/Poised TSS	Fetal Muscle Trunk	muscle
39	chr1:149684000-149684200	Active TSS	Ovary	ovary
40	chr1:149684000-149684200	Active TSS	A549	lung
41	chr1:149684000-149684200	Active TSS	Hela-S3	cervix
42	chr1:149684000-149684200	Active TSS	HepG2	liver
43	chr1:149684000-149684200	Bivalent/Poised TSS	HUVEC	blood vessel
44	chr1:149684000-149684200	Active TSS	Monocytes-CD14+_RO01746	blood
45	chr1:149684000-149684200	Bivalent/Poised TSS	NH-A	brain
46	chr1:149684000-149684200	Bivalent/Poised TSS	Osteobl	bone
47	chr1:149684000-149684400	Enhancers	Primary T helper cells fromperipheralblood	blood
48	chr1:149684000-149684800	Active TSS	iPS-15b Cell Line	embryonic stem cell
49	chr1:149684000-149684800	Active TSS	Adipose Nuclei	Adipose
50	chr1:149684000-149685000	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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