Variant report

Variant	nsv872419
Chromosome Location	chr1:150699199-150738759
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:249)
CpG islands
(count:244)
Chromatin interactive
region (count:18)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:249 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:150721470-150721983	K562	blood:	n/a	n/a
2	ARID3A	chr1:150737188-150737580	HepG2	liver:	n/a	n/a
3	ARID3A	chr1:150735027-150735152	K562	blood:	n/a	n/a
4	ATF1	chr1:150735140-150735301	K562	blood:	n/a	n/a
5	ATF2	chr1:150737922-150738587	GM12878	blood:	n/a	n/a
6	BATF	chr1:150737069-150737330	GM12878	blood:	n/a	n/a
7	BATF	chr1:150738024-150738477	GM12878	blood:	n/a	chr1:150738368-150738377
8	BATF	chr1:150738059-150738510	GM12878	blood:	n/a	chr1:150738368-150738377
9	BCL3	chr1:150738007-150738423	GM12878	blood:	n/a	chr1:150738330-150738339
10	BCLAF1	chr1:150737911-150738457	GM12878	blood:	n/a	chr1:150738330-150738339
11	BCLAF1	chr1:150737934-150738532	GM12878	blood:	n/a	chr1:150738330-150738339
12	BHLHE40	chr1:150738026-150738513	GM12878	blood:	n/a	n/a
13	CCNT2	chr1:150736368-150736679	K562	blood:	n/a	n/a
14	CEBPB	chr1:150737343-150737582	HepG2	liver:	n/a	n/a
15	CEBPB	chr1:150737194-150737676	A549	lung:	n/a	n/a
16	CEBPB	chr1:150718250-150718535	HepG2	liver:	n/a	chr1:150718381-150718392
17	CEBPB	chr1:150736963-150737857	A549	lung:	n/a	n/a
18	CEBPB	chr1:150737110-150737710	IMR90	lung:	n/a	n/a
19	CEBPB	chr1:150737278-150737651	A549	lung:	n/a	n/a
20	CEBPB	chr1:150718259-150718520	IMR90	lung:	n/a	chr1:150718381-150718392
21	CEBPB	chr1:150718307-150718507	K562	blood:	n/a	chr1:150718381-150718392
22	CEBPB	chr1:150737058-150737704	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr1:150718271-150718532	A549	lung:	n/a	chr1:150718381-150718392
24	CHD1	chr1:150736265-150736520	GM12878	blood:	n/a	n/a
25	CHD1	chr1:150737238-150738349	GM12878	blood:	n/a	n/a
26	CHD2	chr1:150722139-150722516	K562	blood:	n/a	n/a
27	CREB1	chr1:150737954-150738573	GM12878	blood:	n/a	n/a
28	CTCF	chr1:150707555-150707627	K562	blood:	n/a	chr1:150707584-150707592 chr1:150707581-150707599
29	CTCF	chr1:150707543-150707641	Hela-S3	cervix:	n/a	chr1:150707584-150707592 chr1:150707581-150707599
30	CTCF	chr1:150727060-150727210	WI-38	lung:	n/a	n/a
31	CTCF	chr1:150732553-150732703	Spleen_OC	spleen:	n/a	n/a
32	CTCF	chr1:150707520-150707670	WERI-Rb-1	eye:	n/a	chr1:150707584-150707592 chr1:150707581-150707599
33	CTCF	chr1:150732556-150732761	GM12878	blood:	n/a	n/a
34	CTCF	chr1:150707575-150707607	K562	blood:	n/a	chr1:150707584-150707592 chr1:150707581-150707599
35	CTCF	chr1:150707460-150707610	AG09319	gingival:	n/a	chr1:150707584-150707592 chr1:150707581-150707599
36	CTCF	chr1:150727129-150727164	GM10248	blood:	n/a	n/a
37	CTCF	chr1:150707540-150707690	GM12872	blood:	n/a	chr1:150707584-150707592 chr1:150707581-150707599
38	CTCF	chr1:150707460-150707610	NHDF-neo	bronchial:	n/a	chr1:150707584-150707592 chr1:150707581-150707599
39	CTCF	chr1:150732460-150732610	GM12872	blood:	n/a	n/a
40	CTCF	chr1:150732606-150732679	GM13976	blood:	n/a	n/a
41	CTCF	chr1:150733427-150733479	GM20000	blood:	n/a	n/a
42	CTCF	chr1:150707520-150707670	AG10803	skin:	n/a	chr1:150707584-150707592 chr1:150707581-150707599
43	CTCF	chr1:150707620-150707770	MCF-7	breast:	n/a	n/a
44	CTCF	chr1:150707440-150707590	HCFaa	heart:	n/a	n/a
45	CTCF	chr1:150707480-150707630	AG09319	gingival:	n/a	chr1:150707584-150707592 chr1:150707581-150707599
46	CTCF	chr1:150715160-150715310	HFF-Myc	foreskin:	n/a	n/a
47	CTCF	chr1:150707480-150707630	NHDF-neo	bronchial:	n/a	chr1:150707584-150707592 chr1:150707581-150707599
48	CTCF	chr1:150732588-150732678	GM13977	blood:	n/a	n/a
49	CTCF	chr1:150732598-150732669	GM10266	blood:	n/a	n/a
50	CTCF	chr1:150738616-150738636	Fibrobl	skin:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:150722805-150722855	PFSK-1	brain:	n/a
2	chr1:150722805-150722855	AG10803	skin:	n/a
3	chr1:150703141-150703191	Hela-S3	cervix:	n/a
4	chr1:150703141-150703191	NHDF-neo	bronchial:	n/a
5	chr1:150722805-150722855	HRCEpiC	kidney:	n/a
6	chr1:150703141-150703191	HUVEC	blood vessel:	n/a
7	chr1:150703141-150703191	SK-N-SH	brain:	n/a
8	chr1:150722805-150722855	HL-60	blood:	n/a
9	chr1:150703141-150703191	Caco-2	colon:	n/a
10	chr1:150722805-150722855	HEEpiC	esophagus:	n/a
11	chr1:150738173-150738223	GM12892	blood:	n/a
12	chr1:150738173-150738223	NHDF-neo	bronchial:	n/a
13	chr1:150703141-150703191	K562	blood:	n/a
14	chr1:150703141-150703191	T-47D	breast:	n/a
15	chr1:150703141-150703191	SK-N-SH_RA	brain:	n/a
16	chr1:150738173-150738223	Hela-S3	cervix:	n/a
17	chr1:150737762-150737812	GM12878	blood:	n/a
18	chr1:150703141-150703191	A549	lung:	n/a
19	chr1:150703141-150703191	IMR90	lung:	fetal
20	chr1:150737762-150737812	HRE	kidney:	n/a
21	chr1:150737762-150737812	H1-hESC	embryonic stem cell:	embryo
22	chr1:150722805-150722855	AG09319	gingival:	n/a
23	chr1:150738173-150738223	GM12878	blood:	n/a
24	chr1:150737762-150737812	A549	lung:	n/a
25	chr1:150737762-150737812	GM19239	blood:	n/a
26	chr1:150738173-150738223	HepG2	liver:	n/a
27	chr1:150703141-150703191	SK-N-MC	brain:	n/a
28	chr1:150722805-150722855	Caco-2	colon:	n/a
29	chr1:150722805-150722855	MCF-7	breast:	n/a
30	chr1:150738173-150738223	NHBE	bronchial:	n/a
31	chr1:150722805-150722855	PANC-1	pancreas:	n/a
32	chr1:150737762-150737812	AG09319	gingival:	n/a
33	chr1:150722805-150722855	SK-N-MC	brain:	n/a
34	chr1:150737762-150737812	HMEC	breast:	n/a
35	chr1:150703141-150703191	HAEpiC	amniotic membrane:	n/a
36	chr1:150703141-150703191	AG04449	skin:	fetal
37	chr1:150703141-150703191	AG09319	gingival:	n/a
38	chr1:150722805-150722855	GM06990	blood:	n/a
39	chr1:150703141-150703191	ECC-1	luminal epithelium:	n/a
40	chr1:150737762-150737812	GM12891	blood:	n/a
41	chr1:150737762-150737812	Caco-2	colon:	n/a
42	chr1:150738173-150738223	HRPEpiC	eye:	n/a
43	chr1:150722805-150722855	NHBE	bronchial:	n/a
44	chr1:150737762-150737812	T-47D	breast:	n/a
45	chr1:150703141-150703191	HCT-116	colon:	n/a
46	chr1:150737762-150737812	Hela-S3	cervix:	n/a
47	chr1:150737762-150737812	GM12892	blood:	n/a
48	chr1:150738173-150738223	BE2_C	brain:	n/a
49	chr1:150703141-150703191	AG04450	lung:	fetal
50	chr1:150722805-150722855	LNCaP	prostate:	n/a

(count:18 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:150724802..150727328-chr1:150746278..150749231,2	MCF-7	breast:
2	chr1:150718367..150722446-chr1:150727232..150730438,3	K562	blood:
3	chr1:150720840..150722838-chr1:150897246..150898815,2	K562	blood:
4	chr1:150731143..150734388-chr1:150735639..150737851,3	MCF-7	breast:
5	chr1:150733435..150736065-chr1:150737703..150739768,2	K562	blood:
6	chr1:150725025..150727549-chr1:150728831..150731687,2	K562	blood:
7	chr1:150688285..150691127-chr1:150698311..150700209,2	K562	blood:
8	chr1:150693906..150695724-chr1:150707796..150710727,2	K562	blood:
9	chr1:150692737..150694366-chr1:150708966..150711892,2	MCF-7	breast:
10	chr1:150718351..150719880-chr1:150768109..150769621,2	K562	blood:
11	chr1:150720934..150724836-chr1:150780473..150783915,3	K562	blood:
12	chr1:150725025..150727549-chr1:150728831..150731687,2	K562	blood:
13	chr1:150718367..150722446-chr1:150727232..150730438,3	K562	blood:
14	chr1:150600704..150602423-chr1:150722921..150725680,2	MCF-7	breast:
15	chr1:150730585..150733903-chr1:150734445..150737358,3	K562	blood:
16	chr1:150638939..150641718-chr1:150729032..150731135,2	K562	blood:
17	chr1:150550688..150552369-chr1:150735871..150738707,2	MCF-7	breast:
18	chr1:150716385..150719781-chr1:150720227..150722599,4	K562	blood:

No data

Variant related genes	Relation type
CTSS	TF binding region
CTSS	CpG island
ENSG00000143452	chromatin interactions
ENSG00000143387	chromatin interactions
ENSG00000143420	chromatin interactions
ENSG00000143379	chromatin interactions
ENSG00000143384	chromatin interactions
ENSG00000163131	chromatin interactions

Extended variants
information (count: 1096 )
Associated
traits (count: 115 )

Variant overlapped rSNPs/rCNVs (count:1096 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12747744	chr1:150699199-150699200	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs587744093	chr1:150699209-150699210	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs35741009	chr1:150699267-150699268	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs148772510	chr1:150699326-150699327	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs76687827	chr1:150699370-150699371	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs587737157	chr1:150699401-150699402	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs587666221	chr1:150699425-150699426	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs201454678	chr1:150699427-150699428	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs146845725	chr1:150699504-150699505	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs181494133	chr1:150699511-150699512	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs199610481	chr1:150699528-150699529	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs187328256	chr1:150699554-150699555	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs587626464	chr1:150699577-150699578	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs7533678	chr1:150699586-150699587	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
15	rs192244670	chr1:150699712-150699713	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs587618057	chr1:150699761-150699762	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs200427461	chr1:150699775-150699776	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs587697970	chr1:150699776-150699777	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs145683069	chr1:150699799-150699800	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs587647188	chr1:150699970-150699971	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs587710599	chr1:150700014-150700015	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs587762955	chr1:150700061-150700062	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs183666672	chr1:150700206-150700207	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs77778303	chr1:150700219-150700220	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs587619516	chr1:150700243-150700244	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs371727100	chr1:150700310-150700311	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs377181619	chr1:150700331-150700332	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs5777735	chr1:150700367-150700368	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs201339672	chr1:150700368-150700369	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs199838487	chr1:150700373-150700374	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs12045672	chr1:150700391-150700392	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs372550472	chr1:150700399-150700400	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs371006011	chr1:150700413-150700414	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs587772809	chr1:150700414-150700415	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs200806664	chr1:150700430-150700431	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs111894119	chr1:150700432-150700433	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs201513194	chr1:150700436-150700437	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs587709791	chr1:150700500-150700501	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs587594230	chr1:150700505-150700506	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs587663941	chr1:150700537-150700538	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs113531449	chr1:150700588-150700589	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs199560313	chr1:150700596-150700597	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs12406409	chr1:150700597-150700598	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs199621380	chr1:150700614-150700615	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs587743053	chr1:150700632-150700633	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs587618345	chr1:150700640-150700641	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs587698268	chr1:150700651-150700652	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs587728110	chr1:150700678-150700679	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs587617569	chr1:150700717-150700718	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs142727277	chr1:150700718-150700719	Weak transcription	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	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
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Gastrointestinal cancer	16790693	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:723 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:150670600-150702600	Weak transcription	Hela-S3	cervix
2	chr1:150681600-150702600	Weak transcription	A549	lung
3	chr1:150690800-150702400	Weak transcription	Primary neutrophils fromperipheralblood	blood
4	chr1:150695000-150702600	Weak transcription	Primary B cells from cord blood	blood
5	chr1:150695200-150702800	Weak transcription	Rectal Mucosa Donor 31	rectum
6	chr1:150696400-150702600	Weak transcription	Primary monocytes fromperipheralblood	blood
7	chr1:150697200-150704400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr1:150697400-150702800	Weak transcription	Primary B cells from peripheral blood	blood
9	chr1:150697600-150705000	Weak transcription	Rectal Mucosa Donor 29	rectum
10	chr1:150698600-150699200	Strong transcription	Monocytes-CD14+_RO01746	blood
11	chr1:150698600-150704400	Weak transcription	Lung	lung
12	chr1:150699200-150702600	Weak transcription	Monocytes-CD14+_RO01746	blood
13	chr1:150700600-150702600	Weak transcription	Primary T helper cells fromperipheralblood	blood
14	chr1:150700600-150704000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
15	chr1:150700800-150704000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
16	chr1:150700800-150704200	Weak transcription	Primary T helper cells PMA-I stimulated	--
17	chr1:150701000-150704000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
18	chr1:150701000-150706000	Weak transcription	Primary T cells from cord blood	blood
19	chr1:150701400-150704400	Weak transcription	Primary T cells fromperipheralblood	blood
20	chr1:150701400-150704400	Weak transcription	Duodenum Mucosa	Duodenum
21	chr1:150701400-150707600	Weak transcription	Primary hematopoietic stem cells	blood
22	chr1:150701400-150708000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
23	chr1:150701400-150710000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
24	chr1:150701400-150727400	Weak transcription	Left Ventricle	heart
25	chr1:150701600-150704800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
26	chr1:150701800-150710400	Weak transcription	Adipose Nuclei	Adipose
27	chr1:150702200-150704200	Weak transcription	GM12878-XiMat	blood
28	chr1:150702400-150702600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
29	chr1:150702400-150704600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
30	chr1:150702400-150707600	Weak transcription	Liver	Liver
31	chr1:150702400-150716200	Strong transcription	Primary neutrophils fromperipheralblood	blood
32	chr1:150702600-150703000	Flanking Active TSS	A549	lung
33	chr1:150702600-150703200	Enhancers	Hela-S3	cervix
34	chr1:150702600-150715800	Strong transcription	Primary T helper cells fromperipheralblood	blood
35	chr1:150702600-150716200	Strong transcription	Primary monocytes fromperipheralblood	blood
36	chr1:150702600-150716200	Strong transcription	Primary B cells from cord blood	blood
37	chr1:150702600-150716200	Strong transcription	Monocytes-CD14+_RO01746	blood
38	chr1:150702800-150703000	Enhancers	Sigmoid Colon	Sigmoid Colon
39	chr1:150702800-150703200	Enhancers	Rectal Mucosa Donor 31	rectum
40	chr1:150702800-150705000	Weak transcription	Fetal Thymus	thymus
41	chr1:150702800-150716200	Strong transcription	Primary B cells from peripheral blood	blood
42	chr1:150703000-150703200	Enhancers	Primary hematopoietic stem cells short term culture	blood
43	chr1:150703000-150703200	Enhancers	A549	lung
44	chr1:150703000-150704400	Weak transcription	Sigmoid Colon	Sigmoid Colon
45	chr1:150703000-150706600	Weak transcription	Spleen	Spleen
46	chr1:150703200-150704400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
47	chr1:150703200-150704400	Weak transcription	Rectal Mucosa Donor 31	rectum
48	chr1:150703200-150705200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
49	chr1:150703200-150709000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
50	chr1:150703200-150713200	Weak transcription	Fetal Intestine Small	intestine

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links