Variant report

Variant	nsv872414
Chromosome Location	chr1:149705399-149768855
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:775)
CpG islands
(count:1162)
Chromatin interactive
region (count:3)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:4)

(count:775 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:149764146-149764192	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:149764085-149764195	K562	blood:	n/a	n/a
3	ARID3A	chr1:149748718-149748918	K562	blood:	n/a	n/a
4	ARID3A	chr1:149747121-149747405	K562	blood:	n/a	n/a
5	ATF1	chr1:149747159-149747411	K562	blood:	n/a	n/a
6	ATF3	chr1:149711658-149712146	A549	lung:	n/a	n/a
7	ATF3	chr1:149711653-149712227	A549	lung:	n/a	n/a
8	ATF3	chr1:149759342-149759524	K562	blood:	n/a	n/a
9	BATF	chr1:149764009-149764293	GM12878	blood:	n/a	n/a
10	BATF	chr1:149743595-149743947	GM12878	blood:	n/a	n/a
11	BATF	chr1:149764414-149764725	GM12878	blood:	n/a	n/a
12	BATF	chr1:149743599-149744024	GM12878	blood:	n/a	n/a
13	BATF	chr1:149736086-149736381	GM12878	blood:	n/a	n/a
14	BATF	chr1:149711785-149712234	GM12878	blood:	n/a	chr1:149711949-149711958
15	BATF	chr1:149711835-149712141	GM12878	blood:	n/a	chr1:149711949-149711958
16	BCL11A	chr1:149743727-149744116	GM12878	blood:	n/a	chr1:149743777-149743786 chr1:149743741-149743750
17	BCL11A	chr1:149764379-149764550	GM12878	blood:	n/a	n/a
18	BCL11A	chr1:149764220-149764668	GM12878	blood:	n/a	n/a
19	BCL11A	chr1:149743550-149744000	GM12878	blood:	n/a	chr1:149743777-149743786 chr1:149743741-149743750
20	BCLAF1	chr1:149764461-149764768	GM12878	blood:	n/a	n/a
21	BHLHE40	chr1:149764150-149764212	GM12878	blood:	n/a	n/a
22	BHLHE40	chr1:149764016-149764210	HepG2	liver:	n/a	n/a
23	BHLHE40	chr1:149764585-149764716	GM12878	blood:	n/a	n/a
24	CBX3	chr1:149759117-149759881	K562	blood:	n/a	n/a
25	CBX3	chr1:149747108-149747994	K562	blood:	n/a	n/a
26	CBX3	chr1:149764404-149764727	K562	blood:	n/a	n/a
27	CBX3	chr1:149759046-149759963	K562	blood:	n/a	n/a
28	CBX3	chr1:149763933-149764334	K562	blood:	n/a	n/a
29	CEBPB	chr1:149711816-149711897	K562	blood:	n/a	chr1:149711854-149711865
30	CEBPB	chr1:149759424-149759816	K562	blood:	n/a	n/a
31	CEBPB	chr1:149764150-149764237	H1-hESC	embryonic stem cell:	n/a	n/a
32	CEBPB	chr1:149747238-149747477	K562	blood:	n/a	n/a
33	CEBPB	chr1:149711785-149711896	HepG2	liver:	n/a	chr1:149711854-149711865
34	CEBPB	chr1:149759101-149760012	K562	blood:	n/a	n/a
35	CEBPB	chr1:149759424-149759644	Hela-S3	cervix:	n/a	n/a
36	CEBPB	chr1:149711697-149712038	A549	lung:	n/a	chr1:149711854-149711865
37	CEBPB	chr1:149711788-149712001	K562	blood:	n/a	chr1:149711854-149711865
38	CEBPB	chr1:149721238-149721393	K562	blood:	n/a	chr1:149721315-149721326 chr1:149721317-149721326
39	CEBPB	chr1:149759308-149759875	K562	blood:	n/a	n/a
40	CEBPB	chr1:149721223-149721399	Hela-S3	cervix:	n/a	chr1:149721315-149721326 chr1:149721317-149721326
41	CEBPB	chr1:149711779-149712003	IMR90	lung:	n/a	chr1:149711854-149711865
42	CEBPB	chr1:149711642-149712210	H1-hESC	embryonic stem cell:	n/a	chr1:149711854-149711865
43	CEBPB	chr1:149764592-149764774	H1-hESC	embryonic stem cell:	n/a	n/a
44	CEBPB	chr1:149711670-149712021	K562	blood:	n/a	chr1:149711854-149711865
45	CEBPB	chr1:149764492-149764695	Hela-S3	cervix:	n/a	n/a
46	CEBPB	chr1:149763981-149764283	K562	blood:	n/a	n/a
47	CEBPB	chr1:149747233-149747432	K562	blood:	n/a	n/a
48	CEBPB	chr1:149764019-149764219	Hela-S3	cervix:	n/a	n/a
49	CEBPD	chr1:149759241-149759973	K562	blood:	n/a	n/a
50	CHD1	chr1:149719574-149719759	H1-hESC	embryonic stem cell:	n/a	n/a

(count:1162 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:149764790-149764840	NB4	blood:	n/a
2	chr1:149764342-149764392	SK-N-SH	brain:	n/a
3	chr1:149719536-149719586	CMK	blood:	n/a
4	chr1:149764790-149764840	NB4	blood:	n/a
5	chr1:149764342-149764392	SK-N-SH	brain:	n/a
6	chr1:149719536-149719586	CMK	blood:	n/a
7	chr1:149765026-149765076	HMEC	breast:	n/a
8	chr1:149753023-149753073	HCPEpiC	choroid plexus:	n/a
9	chr1:149764739-149764789	AG04449	skin:	fetal
10	chr1:149712057-149712107	HCF	heart:	n/a
11	chr1:149758962-149759012	GM06990	blood:	n/a
12	chr1:149720577-149720627	HL-60	blood:	n/a
13	chr1:149717620-149717670	AG10803	skin:	n/a
14	chr1:149719461-149719511	NHDF-neo	bronchial:	n/a
15	chr1:149719243-149719293	Caco-2	colon:	n/a
16	chr1:149718651-149718701	IMR90	lung:	fetal
17	chr1:149764739-149764789	BJ	skin:	n/a
18	chr1:149764342-149764392	AoSMC	blood vessel:	n/a
19	chr1:149764680-149764730	PANC-1	pancreas:	n/a
20	chr1:149717620-149717670	GM12878	blood:	n/a
21	chr1:149764790-149764840	MCF10A-Er-Src	breast:	n/a
22	chr1:149753023-149753073	GM12892	blood:	n/a
23	chr1:149764790-149764840	HEEpiC	esophagus:	n/a
24	chr1:149764680-149764730	MCF-7	breast:	n/a
25	chr1:149764294-149764344	HepG2	liver:	n/a
26	chr1:149712057-149712107	SKMC	muscle:	n/a
27	chr1:149711854-149711904	HIPEpiC	eye:	n/a
28	chr1:149720577-149720627	IMR90	lung:	fetal
29	chr1:149720577-149720627	ProgFib	skin:	n/a
30	chr1:149712057-149712107	HepG2	liver:	n/a
31	chr1:149718651-149718701	BJ	skin:	n/a
32	chr1:149764294-149764344	PrEC	prostate:	n/a
33	chr1:149764342-149764392	HepG2	liver:	n/a
34	chr1:149753023-149753073	HIPEpiC	eye:	n/a
35	chr1:149717620-149717670	RPTEC	kidney:	n/a
36	chr1:149764294-149764344	RPTEC	kidney:	n/a
37	chr1:149719243-149719293	AoSMC	blood vessel:	n/a
38	chr1:149764739-149764789	NT2-D1	testis:	n/a
39	chr1:149758962-149759012	ECC-1	luminal epithelium:	n/a
40	chr1:149767909-149767959	MCF-7	breast:	n/a
41	chr1:149712057-149712107	RPTEC	kidney:	n/a
42	chr1:149765026-149765076	GM12891	blood:	n/a
43	chr1:149719243-149719293	MCF-7	breast:	n/a
44	chr1:149764680-149764730	LNCaP	prostate:	n/a
45	chr1:149717620-149717670	HPAEpiC	pulmonary alveolar:	n/a
46	chr1:149764294-149764344	GM06990	blood:	n/a
47	chr1:149718651-149718701	NHDF-neo	bronchial:	n/a
48	chr1:149767909-149767959	H1-hESC	embryonic stem cell:	embryo
49	chr1:149720577-149720627	NB4	blood:	n/a
50	chr1:149765026-149765076	HIPEpiC	eye:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr1:149758293..149760951-chr1:149816252..149817928,2	K562	blood:
2	chr1:149764705..149766626-chr1:149783077..149785466,2	MCF-7	breast:
3	chr1:146554326..146556624-chr1:149762818..149765682,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-HIST2H2BF-3	chr1:149718450-149720133	NONHSAT006245
2	lnc-HIST2H3D-1	chr1:149757215-149759694	ENSG00000233030.2
3	lnc-HIST2H3D-1	chr1:149763514-149764576	ENSG00000233030.2
4	lnc-HIST2H4A-3	chr1:149754284-149754330	NONHSAT006247
5	lnc-HIST2H4A-2	chr1:149762793-149763231	NONHSAT006250
6	lnc-HIST2H3D-2	chr1:149754433-149754816	ENSG00000242663.1
7	lnc-HIST2H4A-3	chr1:149754726-149755507	NONHSAT006247
8	lnc-HIST2H4A-2	chr1:149761924-149761961	NONHSAT006250
9	lnc-HIST2H2BF-3	chr1:149713129-149713281	NONHSAT006245

No data

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

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

Variant related genes	Relation type
ENSG00000234232	TF binding region
FCGR1A	TF binding region
ENSG00000263825	TF binding region
ENSG00000233030	TF binding region
ENSG00000226500	TF binding region
ENSG00000234232	CpG island
FCGR1A	CpG island
ENSG00000263825	CpG island
ENSG00000233030	CpG island
ENSG00000226500	CpG island
ENSG00000272993	chromatin interactions
ENSG00000242663	chromatin interactions
ENSG00000183598	chromatin interactions
ENSG00000203814	chromatin interactions
ENSG00000230832	chromatin interactions

Extended variants
information (count: 2134 )
Associated
traits (count: 115 )

Variant overlapped rSNPs/rCNVs (count:2134 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs587727463	chr1:149705444-149705445	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs587623599	chr1:149705463-149705464	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs587649392	chr1:149705494-149705495	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs1123717	chr1:149705515-149705516	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs587712846	chr1:149705548-149705549	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs587607177	chr1:149705594-149705595	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs1123718	chr1:149705609-149705610	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs113005921	chr1:149705616-149705617	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs371933958	chr1:149705629-149705630	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs77307500	chr1:149705672-149705673	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs587738446	chr1:149705675-149705676	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs587601318	chr1:149705752-149705753	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs199531529	chr1:149705990-149705991	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs6703698	chr1:149705997-149705998	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs587677658	chr1:149706108-149706109	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs587735024	chr1:149706114-149706115	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs587628310	chr1:149706124-149706125	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs148361587	chr1:149706175-149706176	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs113959027	chr1:149706176-149706177	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs201510753	chr1:149706256-149706257	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs587741583	chr1:149706336-149706337	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs185934293	chr1:149706345-149706346	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs6657763	chr1:149706357-149706358	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs587692265	chr1:149706373-149706374	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs372137389	chr1:149706399-149706400	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs587770735	chr1:149706415-149706416	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
27	rs587669019	chr1:149706478-149706479	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
28	rs587703320	chr1:149706496-149706497	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
29	rs587772778	chr1:149706504-149706505	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
30	rs587656539	chr1:149706517-149706518	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
31	rs587707870	chr1:149706526-149706527	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
32	rs587770023	chr1:149706542-149706543	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
33	rs587634996	chr1:149706584-149706585	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
34	rs200032405	chr1:149706590-149706591	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
35	rs587722544	chr1:149706592-149706593	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
36	rs61806467	chr1:149706610-149706611	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs587677773	chr1:149706611-149706612	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs587708352	chr1:149706651-149706652	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs1923003	chr1:149706656-149706657	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs7520995	chr1:149706658-149706659	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs1339943	chr1:149706676-149706677	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs202065521	chr1:149706689-149706690	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs1339944	chr1:149706729-149706730	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs587608246	chr1:149706752-149706753	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs587664556	chr1:149706762-149706763	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs200076267	chr1:149706809-149706810	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs587732440	chr1:149706815-149706816	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs587613814	chr1:149706838-149706839	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs587664007	chr1:149706855-149706856	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs4247153	chr1:149706878-149706879	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:115)

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
Cancer	23975201	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:602 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:149705400-149707000	Enhancers	Primary monocytes fromperipheralblood	blood
2	chr1:149706400-149706600	Bivalent Enhancer	Esophagus	oesophagus
3	chr1:149706400-149706800	Enhancers	Monocytes-CD14+_RO01746	blood
4	chr1:149707000-149711600	Weak transcription	Primary monocytes fromperipheralblood	blood
5	chr1:149711400-149711600	Enhancers	Primary neutrophils fromperipheralblood	blood
6	chr1:149711600-149711800	Enhancers	Primary T cells fromperipheralblood	blood
7	chr1:149711600-149711800	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr1:149711600-149711800	Enhancers	Placenta	Placenta
9	chr1:149711600-149712000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr1:149711600-149712000	Active TSS	HUES64 Cell Line	embryonic stem cell
11	chr1:149711600-149712000	Active TSS	Primary T helper naive cells from peripheral blood	blood
12	chr1:149711600-149712000	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
13	chr1:149711600-149712200	Active TSS	HUES48 Cell Line	embryonic stem cell
14	chr1:149711600-149712200	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr1:149711600-149712200	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
16	chr1:149711600-149712200	Enhancers	Primary B cells from cord blood	blood
17	chr1:149711600-149712400	Active TSS	HUES6 Cell Line	embryonic stem cell
18	chr1:149711600-149712400	Active TSS	iPS-18 Cell Line	embryonic stem cell
19	chr1:149711600-149712400	Enhancers	Primary monocytes fromperipheralblood	blood
20	chr1:149711600-149712400	Active TSS	Monocytes-CD14+_RO01746	blood
21	chr1:149711600-149712400	Active TSS	NHEK	skin
22	chr1:149711600-149712600	Active TSS	ES-I3 Cell Line	embryonic stem cell
23	chr1:149711600-149712600	Active TSS	H1 Cell Line	embryonic stem cell
24	chr1:149711600-149712600	Active TSS	H9 Cell Line	embryonic stem cell
25	chr1:149711600-149712600	Active TSS	iPS-15b Cell Line	embryonic stem cell
26	chr1:149711600-149712600	Active TSS	A549	lung
27	chr1:149711800-149712000	Bivalent/Poised TSS	IMR90 fetal lung fibroblasts Cell Line	lung
28	chr1:149711800-149712000	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
29	chr1:149711800-149712000	Active TSS	Primary T helper 17 cells PMA-I stimulated	--
30	chr1:149711800-149712000	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
31	chr1:149711800-149712000	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
32	chr1:149711800-149712000	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
33	chr1:149711800-149712000	Flanking Bivalent TSS/Enh	Duodenum Smooth Muscle	Duodenum
34	chr1:149711800-149712000	Flanking Active TSS	Placenta	Placenta
35	chr1:149711800-149712000	Active TSS	Pancreas	Pancrea
36	chr1:149711800-149712000	Active TSS	GM12878-XiMat	blood
37	chr1:149711800-149712200	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
38	chr1:149711800-149712200	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr1:149711800-149712200	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
40	chr1:149711800-149712200	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
41	chr1:149711800-149712200	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
42	chr1:149711800-149712200	Flanking Active TSS	Primary T cells fromperipheralblood	blood
43	chr1:149711800-149712200	Active TSS	Primary T regulatory cells fromperipheralblood	blood
44	chr1:149711800-149712200	Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
45	chr1:149711800-149712200	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
46	chr1:149711800-149712200	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin01	Skin
47	chr1:149711800-149712200	Bivalent/Poised TSS	Foreskin Melanocyte Primary Cells skin03	Skin
48	chr1:149711800-149712200	Active TSS	Primary mononuclear cells fromperipheralblood	Blood
49	chr1:149711800-149712200	Active TSS	Adipose Nuclei	Adipose
50	chr1:149711800-149712200	Active TSS	Brain Inferior Temporal Lobe	brain

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