Variant report

Variant	nsv947547
Chromosome Location	chr1:155698814-155708436
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:346)
CpG islands
(count:122)
Chromatin interactive
region (count:3)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:346 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr1:155698936-155699152	H1-hESC	embryonic stem cell:	n/a	n/a
2	CEBPB	chr1:155702817-155702837	K562	blood:	n/a	n/a
3	CEBPB	chr1:155699390-155699594	A549	lung:	n/a	chr1:155699525-155699536
4	CEBPB	chr1:155706227-155706258	H1-hESC	embryonic stem cell:	n/a	n/a
5	CEBPB	chr1:155699386-155699687	HepG2	liver:	n/a	chr1:155699525-155699536
6	CEBPB	chr1:155699430-155699564	HepG2	liver:	n/a	chr1:155699525-155699536
7	CEBPB	chr1:155699353-155699676	MCF-7	breast:	n/a	chr1:155699525-155699536
8	CEBPB	chr1:155699435-155699660	HepG2	liver:	n/a	chr1:155699525-155699536
9	CEBPB	chr1:155699439-155699554	K562	blood:	n/a	chr1:155699525-155699536
10	CEBPB	chr1:155699401-155699642	IMR90	lung:	n/a	chr1:155699525-155699536
11	CTCF	chr1:155698920-155699070	A549	lung:	n/a	n/a
12	CTCF	chr1:155701580-155701730	A549	lung:	n/a	n/a
13	CTCF	chr1:155707857-155708172	T-47D	breast:	n/a	n/a
14	CTCF	chr1:155698973-155699195	GM10266	blood:	n/a	n/a
15	CTCF	chr1:155698931-155699242	GM12878	blood:	n/a	n/a
16	CTCF	chr1:155698898-155699274	GM12878	blood:	n/a	n/a
17	CTCF	chr1:155699020-155699170	HCFaa	heart:	n/a	n/a
18	CTCF	chr1:155698972-155699156	SK-N-SH_RA	brain:	n/a	n/a
19	CTCF	chr1:155698702-155699367	MCF-7	breast:	n/a	n/a
20	CTCF	chr1:155699020-155699170	HepG2	liver:	n/a	n/a
21	CTCF	chr1:155699420-155699570	HEK293	kidney:	n/a	n/a
22	CTCF	chr1:155701640-155701790	AG04449	skin:	n/a	n/a
23	CTCF	chr1:155699028-155699055	H1-hESC	embryonic stem cell:	n/a	n/a
24	CTCF	chr1:155699040-155699190	AoAF	blood vessel:	n/a	n/a
25	CTCF	chr1:155698940-155699090	HMEC	breast:	n/a	n/a
26	CTCF	chr1:155699020-155699170	AG10803	skin:	n/a	n/a
27	CTCF	chr1:155698956-155699184	Hela-S3	cervix:	n/a	n/a
28	CTCF	chr1:155699080-155699230	NHEK	skin:	n/a	n/a
29	CTCF	chr1:155699040-155699190	HFF	foreskin:	n/a	n/a
30	CTCF	chr1:155698955-155699207	Lung_OC	lung:	n/a	n/a
31	CTCF	chr1:155699060-155699210	HFF-Myc	foreskin:	n/a	n/a
32	CTCF	chr1:155699040-155699190	GM12874	blood:	n/a	n/a
33	CTCF	chr1:155699020-155699170	RPTEC	kidney:	n/a	n/a
34	CTCF	chr1:155698940-155699131	A549	lung:	n/a	n/a
35	CTCF	chr1:155701693-155701830	GM19240	blood:	n/a	n/a
36	CTCF	chr1:155699020-155699170	AoAF	blood vessel:	n/a	n/a
37	CTCF	chr1:155699000-155699150	SK-N-SH_RA	brain:	n/a	n/a
38	CTCF	chr1:155699020-155699170	BJ	skin:	n/a	n/a
39	CTCF	chr1:155698980-155699130	WERI-Rb-1	eye:	n/a	n/a
40	CTCF	chr1:155701580-155701730	HRE	kidney:	n/a	n/a
41	CTCF	chr1:155698970-155699229	Spleen_OC	spleen:	n/a	n/a
42	CTCF	chr1:155699000-155699150	Caco-2	colon:	n/a	n/a
43	CTCF	chr1:155701700-155701850	K562	blood:	n/a	n/a
44	CTCF	chr1:155699020-155699170	GM12875	blood:	n/a	n/a
45	CTCF	chr1:155699000-155699150	HRE	kidney:	n/a	n/a
46	CTCF	chr1:155701640-155701790	HMF	breast:	n/a	n/a
47	CTCF	chr1:155699020-155699170	BE2_C	brain:	n/a	n/a
48	CTCF	chr1:155701620-155701770	MCF-7	breast:	n/a	n/a
49	CTCF	chr1:155699040-155699190	GM12870	blood:	n/a	n/a
50	CTCF	chr1:155701680-155701830	AG09309	skin:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:155708104-155708154	HCPEpiC	choroid plexus:	n/a
2	chr1:155708104-155708154	SAEC	small airway:	n/a
3	chr1:155699008-155699058	HIPEpiC	eye:	n/a
4	chr1:155708104-155708154	AoSMC	blood vessel:	n/a
5	chr1:155699008-155699058	SKMC	muscle:	n/a
6	chr1:155699008-155699058	SK-N-MC	brain:	n/a
7	chr1:155699008-155699058	NH-A	brain:	n/a
8	chr1:155708104-155708154	NHBE	bronchial:	n/a
9	chr1:155699008-155699058	NB4	blood:	n/a
10	chr1:155708104-155708154	Caco-2	colon:	n/a
11	chr1:155699008-155699058	HRCEpiC	kidney:	n/a
12	chr1:155708104-155708154	SK-N-SH	brain:	n/a
13	chr1:155699008-155699058	HCF	heart:	n/a
14	chr1:155699008-155699058	HCPEpiC	choroid plexus:	n/a
15	chr1:155699008-155699058	CMK	blood:	n/a
16	chr1:155708104-155708154	NH-A	brain:	n/a
17	chr1:155699008-155699058	PFSK-1	brain:	n/a
18	chr1:155708104-155708154	HRPEpiC	eye:	n/a
19	chr1:155708104-155708154	GM12878	blood:	n/a
20	chr1:155699008-155699058	AG10803	skin:	n/a
21	chr1:155708104-155708154	RPTEC	kidney:	n/a
22	chr1:155699008-155699058	HAEpiC	amniotic membrane:	n/a
23	chr1:155699008-155699058	PANC-1	pancreas:	n/a
24	chr1:155699008-155699058	BE2_C	brain:	n/a
25	chr1:155699008-155699058	AoSMC	blood vessel:	n/a
26	chr1:155708104-155708154	HEEpiC	esophagus:	n/a
27	chr1:155699008-155699058	HEEpiC	esophagus:	n/a
28	chr1:155699008-155699058	NHBE	bronchial:	n/a
29	chr1:155699008-155699058	T-47D	breast:	n/a
30	chr1:155699008-155699058	SK-N-SH_RA	brain:	n/a
31	chr1:155708104-155708154	Jurkat	blood:	n/a
32	chr1:155708104-155708154	GM12892	blood:	n/a
33	chr1:155708104-155708154	BE2_C	brain:	n/a
34	chr1:155708104-155708154	HCF	heart:	n/a
35	chr1:155708104-155708154	HCM	heart:	n/a
36	chr1:155708104-155708154	HEK293	kidney:	embryo
37	chr1:155708104-155708154	U87	brain:	n/a
38	chr1:155708104-155708154	SK-N-MC	brain:	n/a
39	chr1:155699008-155699058	HRPEpiC	eye:	n/a
40	chr1:155699008-155699058	HRE	kidney:	n/a
41	chr1:155699008-155699058	GM06990	blood:	n/a
42	chr1:155708104-155708154	HCT-116	colon:	n/a
43	chr1:155699008-155699058	Hepatocyte	liver:	n/a
44	chr1:155708104-155708154	T-47D	breast:	n/a
45	chr1:155699008-155699058	HCM	heart:	n/a
46	chr1:155708104-155708154	MCF-7	breast:	n/a
47	chr1:155699008-155699058	AG09309	skin:	n/a
48	chr1:155699008-155699058	HCT-116	colon:	n/a
49	chr1:155708104-155708154	GM06990	blood:	n/a
50	chr1:155699008-155699058	GM19239	blood:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr1:155699238..155701661-chr1:155707272..155709440,2	K562	blood:
2	chr1:155699238..155701661-chr1:155707272..155709440,2	K562	blood:
3	chr1:155704457..155706134-chr1:155713867..155715519,2	MCF-7	breast:

No data

Variant related genes	Relation type
DAP3	TF binding region
DAP3	CpG island

Extended variants
information (count: 357 )
Associated
traits (count: 99 )

Variant overlapped rSNPs/rCNVs (count:357 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs371263118	chr1:155698850-155698851	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs545683945	chr1:155698852-155698853	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs367821120	chr1:155698895-155698896	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs200267442	chr1:155698917-155698918	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs376225469	chr1:155698929-155698930	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs201265692	chr1:155698940-155698941	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs368325239	chr1:155698943-155698944	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs375216873	chr1:155698945-155698946	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs367572641	chr1:155698947-155698948	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs372817713	chr1:155698961-155698962	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs144563957	chr1:155698978-155698979	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs201155259	chr1:155698986-155698987	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs370718586	chr1:155698994-155698995	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs552936757	chr1:155699005-155699006	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs200984755	chr1:155699008-155699009	Weak transcription Strong transcription Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
16	rs145328544	chr1:155699009-155699010	Weak transcription Strong transcription Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
17	rs373985177	chr1:155699011-155699012	Weak transcription Strong transcription Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
18	rs147699097	chr1:155699030-155699031	Weak transcription Strong transcription Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
19	rs57692591	chr1:155699032-155699033	Weak transcription Strong transcription Enhancers	TF binding region CpG island	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs377654022	chr1:155699053-155699054	Weak transcription Strong transcription Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
21	rs371226776	chr1:155699057-155699058	Weak transcription Strong transcription Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
22	rs1802736	chr1:155699073-155699074	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs569405423	chr1:155699097-155699098	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs536698370	chr1:155699098-155699099	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs4933	chr1:155699118-155699119	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs375689451	chr1:155699156-155699157	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs145213844	chr1:155699158-155699159	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs367639956	chr1:155699167-155699168	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs373171130	chr1:155699174-155699175	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs141810300	chr1:155699187-155699188	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs370880846	chr1:155699205-155699206	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs542193562	chr1:155699256-155699257	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs181085427	chr1:155699274-155699275	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs553607252	chr1:155699309-155699310	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs578258368	chr1:155699351-155699352	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs545410717	chr1:155699426-155699427	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs563719424	chr1:155699427-155699428	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs115851291	chr1:155699428-155699429	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs561944020	chr1:155699432-155699433	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs530931986	chr1:155699514-155699515	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs143453428	chr1:155699566-155699567	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs116237120	chr1:155699598-155699599	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs185876011	chr1:155699645-155699646	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs541384657	chr1:155699648-155699649	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs547097392	chr1:155699649-155699650	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs565625444	chr1:155699689-155699690	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs533101480	chr1:155699703-155699704	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs10908480	chr1:155699762-155699763	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
49	rs569266343	chr1:155699803-155699804	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs189469876	chr1:155699825-155699826	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:99)

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
Liposarcoma	21253554	CNVD
Non-small cell lung cancer	21385341	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	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
Non-syndromic sensorineural hearing loss	15273396	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
Ewing''s sarcoma	21437220	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
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
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
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
Testicular germ cell tumor	18059402	CNVD
Trisomy 5 syndrome	21098271	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Glioblastoma multiforme	21138945	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21611746	CNVD
Neuroblastoma	18923191	CNVD
Myelofibrosis	22110671	CNVD
Liver carcinoma	19366792	CNVD
Dihydropyrimidine dehydrogenase deficiency	18421352	CNVD

Chromatin state (count:459 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:155660400-155706200	Weak transcription	Colonic Mucosa	Colon
2	chr1:155661600-155707800	Weak transcription	HUVEC	blood vessel
3	chr1:155663200-155701000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
4	chr1:155665200-155708000	Weak transcription	Placenta Amnion	Placenta Amnion
5	chr1:155665400-155699000	Weak transcription	Right Ventricle	heart
6	chr1:155665600-155707200	Weak transcription	Psoas Muscle	Psoas
7	chr1:155665800-155707000	Weak transcription	Small Intestine	intestine
8	chr1:155669200-155702200	Weak transcription	Gastric	stomach
9	chr1:155673800-155707800	Weak transcription	Aorta	Aorta
10	chr1:155676400-155706200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
11	chr1:155677400-155705200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr1:155679400-155710400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
13	chr1:155679800-155704200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
14	chr1:155681600-155707800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
15	chr1:155683000-155703200	Weak transcription	Spleen	Spleen
16	chr1:155683200-155715000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr1:155683400-155699200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
18	chr1:155683400-155707800	Weak transcription	Fetal Heart	heart
19	chr1:155683800-155709000	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
20	chr1:155683800-155715000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr1:155684000-155700000	Weak transcription	Rectal Mucosa Donor 31	rectum
22	chr1:155684000-155707800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
23	chr1:155685200-155704800	Strong transcription	Fetal Thymus	thymus
24	chr1:155687200-155715000	Weak transcription	Esophagus	oesophagus
25	chr1:155687600-155699200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
26	chr1:155688400-155705000	Strong transcription	Primary hematopoietic stem cells short term culture	blood
27	chr1:155688400-155711200	Strong transcription	Fetal Muscle Leg	muscle
28	chr1:155688800-155710800	Strong transcription	Fetal Stomach	stomach
29	chr1:155688800-155711000	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
30	chr1:155689200-155706000	Weak transcription	Fetal Brain Male	brain
31	chr1:155689200-155709400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr1:155689800-155701400	Weak transcription	Brain Germinal Matrix	brain
33	chr1:155690200-155706200	Weak transcription	Lung	lung
34	chr1:155690600-155702800	Weak transcription	Fetal Lung	lung
35	chr1:155691000-155709000	Strong transcription	HUES64 Cell Line	embryonic stem cell
36	chr1:155691200-155704600	Strong transcription	Placenta	Placenta
37	chr1:155691200-155705200	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
38	chr1:155691800-155706200	Weak transcription	NHDF-Ad	bronchial
39	chr1:155692000-155700200	Weak transcription	Primary hematopoietic stem cells	blood
40	chr1:155692200-155706200	Weak transcription	Ovary	ovary
41	chr1:155693200-155699400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr1:155693400-155699000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
43	chr1:155693400-155699000	Weak transcription	Primary B cells from peripheral blood	blood
44	chr1:155693800-155704800	Strong transcription	HUES48 Cell Line	embryonic stem cell
45	chr1:155694000-155702600	Weak transcription	Thymus	Thymus
46	chr1:155694800-155700400	Strong transcription	Sigmoid Colon	Sigmoid Colon
47	chr1:155694800-155704400	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
48	chr1:155694800-155704600	Strong transcription	Dnd41	blood
49	chr1:155694800-155704600	Strong transcription	Hela-S3	cervix
50	chr1:155694800-155705000	Strong transcription	Primary T helper cells fromperipheralblood	blood

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