Variant report

Variant	nsv524157
Chromosome Location	chr1:155026942-155030557
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:75)
CpG islands
(count:184)
Chromatin interactive
region (count:7)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:75 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr1:155027464-155027610	A549	lung:	n/a	n/a
2	CTCF	chr1:155030540-155030690	HEK293	kidney:	n/a	n/a
3	CTCF	chr1:155030520-155030670	GM12871	blood:	n/a	n/a
4	CTCF	chr1:155030480-155030630	HepG2	liver:	n/a	n/a
5	CTCF	chr1:155030520-155030670	GM12873	blood:	n/a	n/a
6	CTCF	chr1:155030554-155030657	Hela-S3	cervix:	n/a	n/a
7	CTCF	chr1:155030520-155030670	AoAF	blood vessel:	n/a	n/a
8	CTCF	chr1:155030520-155030670	GM12866	blood:	n/a	n/a
9	CTCF	chr1:155030480-155030630	HMF	breast:	n/a	n/a
10	CTCF	chr1:155030520-155030670	SK-N-SH_RA	brain:	n/a	n/a
11	CTCF	chr1:155030460-155030610	HCT-116	colon:	n/a	n/a
12	CTCF	chr1:155030500-155030650	HA-sp	spinal cord:	n/a	n/a
13	CTCF	chr1:155030400-155030550	BJ	skin:	n/a	n/a
14	CTCF	chr1:155030500-155030650	Caco-2	colon:	n/a	n/a
15	CTCF	chr1:155030540-155030690	GM12864	blood:	n/a	n/a
16	CTCF	chr1:155030480-155030630	GM12864	blood:	n/a	n/a
17	CTCF	chr1:155030525-155030687	T-47D	breast:	n/a	n/a
18	CTCF	chr1:155030529-155030654	MCF-7	breast:	n/a	n/a
19	CTCF	chr1:155030500-155030650	HBMEC	blood vessel:	n/a	n/a
20	CTCF	chr1:155030540-155030690	GM12865	blood:	n/a	n/a
21	CTCF	chr1:155030480-155030630	SAEC	small airway:	n/a	n/a
22	CTCF	chr1:155030540-155030690	HAc	cerebellar:	n/a	n/a
23	CTCF	chr1:155030520-155030670	NB4	blood:	n/a	n/a
24	CTCF	chr1:155030480-155030630	K562	blood:	n/a	n/a
25	CTCF	chr1:155030480-155030630	HCFaa	heart:	n/a	n/a
26	CTCF	chr1:155030520-155030670	GM12872	blood:	n/a	n/a
27	CTCF	chr1:155030500-155030650	Hela-S3	cervix:	n/a	n/a
28	CTCF	chr1:155030440-155030590	HEK293	kidney:	n/a	n/a
29	CTCF	chr1:155030540-155030690	NHEK	skin:	n/a	n/a
30	CTCF	chr1:155030460-155030610	GM12866	blood:	n/a	n/a
31	CTCF	chr1:155030540-155030690	AG04449	skin:	n/a	n/a
32	CTCF	chr1:155030540-155030690	AG09319	gingival:	n/a	n/a
33	CTCF	chr1:155030460-155030610	HCPEpiC	choroid plexus:	n/a	n/a
34	CTCF	chr1:155030480-155030630	GM12865	blood:	n/a	n/a
35	CTCF	chr1:155030520-155030670	HRPEpiC	eye:	n/a	n/a
36	CTCF	chr1:155030520-155030670	AG04449	skin:	n/a	n/a
37	CTCF	chr1:155030540-155030690	HVMF	connective:	n/a	n/a
38	CTCF	chr1:155030480-155030630	WERI-Rb-1	eye:	n/a	n/a
39	CTCF	chr1:155030211-155030855	A549	lung:	n/a	n/a
40	CTCF	chr1:155030500-155030650	GM12873	blood:	n/a	n/a
41	CTCF	chr1:155030540-155030690	AG10803	skin:	n/a	n/a
42	CTCF	chr1:155030540-155030690	RPTEC	kidney:	n/a	n/a
43	CTCF	chr1:155030540-155030690	GM12878	blood:	n/a	n/a
44	CTCF	chr1:155030460-155030610	GM12865	blood:	n/a	n/a
45	CTCF	chr1:155030540-155030690	AG04450	lung:	n/a	n/a
46	CTCF	chr1:155030500-155030650	BE2_C	brain:	n/a	n/a
47	CTCF	chr1:155030540-155030690	BE2_C	brain:	n/a	n/a
48	CTCF	chr1:155030320-155030470	HFF	foreskin:	n/a	n/a
49	CTCF	chr1:155030540-155030690	MCF-7	breast:	n/a	n/a
50	CTCF	chr1:155030240-155030390	K562	blood:	n/a	n/a

(count:184 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:155029748-155029798	NH-A	brain:	n/a
2	chr1:155029748-155029798	NH-A	brain:	n/a
3	chr1:155029748-155029798	T-47D	breast:	n/a
4	chr1:155029748-155029798	NHBE	bronchial:	n/a
5	chr1:155029748-155029798	SKMC	muscle:	n/a
6	chr1:155028224-155028274	BJ	skin:	n/a
7	chr1:155030096-155030146	LNCaP	prostate:	n/a
8	chr1:155030096-155030146	GM12892	blood:	n/a
9	chr1:155029748-155029798	RPTEC	kidney:	n/a
10	chr1:155029748-155029798	MCF-7	breast:	n/a
11	chr1:155028224-155028274	Caco-2	colon:	n/a
12	chr1:155028224-155028274	HRE	kidney:	n/a
13	chr1:155030096-155030146	Caco-2	colon:	n/a
14	chr1:155029748-155029798	Caco-2	colon:	n/a
15	chr1:155029748-155029798	PFSK-1	brain:	n/a
16	chr1:155028224-155028274	SK-N-SH_RA	brain:	n/a
17	chr1:155029748-155029798	AG10803	skin:	n/a
18	chr1:155028224-155028274	Hepatocyte	liver:	n/a
19	chr1:155028224-155028274	H1-hESC	embryonic stem cell:	embryo
20	chr1:155029748-155029798	HRE	kidney:	n/a
21	chr1:155030096-155030146	HPAEpiC	pulmonary alveolar:	n/a
22	chr1:155030096-155030146	HAEpiC	amniotic membrane:	n/a
23	chr1:155028224-155028274	AoSMC	blood vessel:	n/a
24	chr1:155028224-155028274	CMK	blood:	n/a
25	chr1:155028224-155028274	T-47D	breast:	n/a
26	chr1:155030096-155030146	AoSMC	blood vessel:	n/a
27	chr1:155028224-155028274	NHBE	bronchial:	n/a
28	chr1:155029748-155029798	AG09319	gingival:	n/a
29	chr1:155030096-155030146	RPTEC	kidney:	n/a
30	chr1:155028224-155028274	ProgFib	skin:	n/a
31	chr1:155029748-155029798	CMK	blood:	n/a
32	chr1:155030096-155030146	SKMC	muscle:	n/a
33	chr1:155030096-155030146	K562	blood:	n/a
34	chr1:155029748-155029798	HPAEpiC	pulmonary alveolar:	n/a
35	chr1:155030096-155030146	T-47D	breast:	n/a
36	chr1:155029748-155029798	GM12891	blood:	n/a
37	chr1:155029748-155029798	SK-N-SH_RA	brain:	n/a
38	chr1:155029748-155029798	ECC-1	luminal epithelium:	n/a
39	chr1:155029748-155029798	H1-hESC	embryonic stem cell:	embryo
40	chr1:155028224-155028274	Hela-S3	cervix:	n/a
41	chr1:155028224-155028274	HRCEpiC	kidney:	n/a
42	chr1:155028224-155028274	NB4	blood:	n/a
43	chr1:155030096-155030146	GM06990	blood:	n/a
44	chr1:155029748-155029798	NHDF-neo	bronchial:	n/a
45	chr1:155030096-155030146	H1-hESC	embryonic stem cell:	embryo
46	chr1:155028224-155028274	HepG2	liver:	n/a
47	chr1:155029748-155029798	PANC-1	pancreas:	n/a
48	chr1:155030096-155030146	HL-60	blood:	n/a
49	chr1:155030096-155030146	NH-A	brain:	n/a
50	chr1:155028224-155028274	NHDF-neo	bronchial:	n/a

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:154968418..154978887-chr1:155021582..155027516,28	MCF-7	breast:
2	chr1:154971124..154975632-chr1:155030158..155034057,4	K562	blood:
3	chr1:155013927..155032770-chr1:155044175..155061131,53	MCF-7	breast:
4	chr1:154993321..154996248-chr1:155024180..155027135,2	K562	blood:
5	chr1:154969072..154977664-chr1:155030052..155039846,22	MCF-7	breast:
6	chr1:154990094..154990641-chr1:155030119..155030672,2	MCF-7	breast:
7	chr1:154954733..154957486-chr1:155027270..155029022,2	MCF-7	breast:

No data

Variant related genes	Relation type
ADAM15	TF binding region
ADAM15	CpG island
ENSG00000160685	chromatin interactions
ENSG00000143590	chromatin interactions
ENSG00000160688	chromatin interactions

Extended variants
information (count: 177 )
Associated
traits (count: 108 )

Variant overlapped rSNPs/rCNVs (count:177 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6427128	chr1:155026942-155026943	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs201298826	chr1:155026947-155026948	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs199668516	chr1:155026952-155026953	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs375179736	chr1:155026958-155026959	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs369194195	chr1:155026978-155026979	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs200391048	chr1:155026980-155026981	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs189434769	chr1:155026998-155026999	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs377279938	chr1:155027003-155027004	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs528070132	chr1:155027077-155027078	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs145815601	chr1:155027082-155027083	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs138716554	chr1:155027087-155027088	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs370343563	chr1:155027124-155027125	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs181751953	chr1:155027129-155027130	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs142769535	chr1:155027152-155027153	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs569036944	chr1:155027219-155027220	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs541327779	chr1:155027220-155027221	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs144536711	chr1:155027246-155027247	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs548656444	chr1:155027247-155027248	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs564723011	chr1:155027261-155027262	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs533933089	chr1:155027288-155027289	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs185910762	chr1:155027329-155027330	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs542944861	chr1:155027422-155027423	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs191232888	chr1:155027469-155027470	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs529460801	chr1:155027477-155027478	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs538504615	chr1:155027552-155027553	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs549507497	chr1:155027585-155027586	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs556498526	chr1:155027644-155027645	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs138192299	chr1:155027694-155027695	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs66745251	chr1:155027695-155027696	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs71586049	chr1:155027711-155027712	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs574654181	chr1:155027716-155027717	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs71077976	chr1:155027718-155027719	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs10158328	chr1:155027763-155027764	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs554231227	chr1:155027766-155027767	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs572537834	chr1:155027771-155027772	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs539823786	chr1:155027772-155027773	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs564868673	chr1:155027803-155027804	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs141743658	chr1:155027863-155027864	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs551687581	chr1:155027904-155027905	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs562675262	chr1:155027924-155027925	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs183141525	chr1:155028005-155028006	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs150578376	chr1:155028011-155028012	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs186050245	chr1:155028032-155028033	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs527714627	chr1:155028040-155028041	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs570098964	chr1:155028097-155028098	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs113705368	chr1:155028133-155028134	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs182143574	chr1:155028151-155028152	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs539088677	chr1:155028207-155028208	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs139975266	chr1:155028228-155028229	Weak transcription Strong transcription Genic enhancers	CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs199777219	chr1:155028235-155028236	Weak transcription Strong transcription Genic enhancers	CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:108)

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	20409316	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
Chronic lymphocytic leukemia	22228453	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
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:179 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:155024800-155028200	Weak transcription	Aorta	Aorta
2	chr1:155025000-155034200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr1:155025200-155028200	Weak transcription	Liver	Liver
4	chr1:155025200-155028200	Weak transcription	HSMMtube	muscle
5	chr1:155025200-155028200	Weak transcription	NHLF	lung
6	chr1:155025200-155028400	Weak transcription	Colon Smooth Muscle	Colon
7	chr1:155025200-155028600	Weak transcription	Brain Angular Gyrus	brain
8	chr1:155025200-155028600	Weak transcription	Small Intestine	intestine
9	chr1:155025200-155034000	Weak transcription	NH-A	brain
10	chr1:155025200-155034200	Weak transcription	Psoas Muscle	Psoas
11	chr1:155025200-155034200	Weak transcription	NHDF-Ad	bronchial
12	chr1:155025400-155027000	Enhancers	Primary hematopoietic stem cells	blood
13	chr1:155025400-155027000	Weak transcription	Osteobl	bone
14	chr1:155025400-155028200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr1:155025400-155028200	Weak transcription	Placenta Amnion	Placenta Amnion
16	chr1:155025400-155028200	Weak transcription	Rectal Smooth Muscle	rectum
17	chr1:155025400-155028600	Weak transcription	HepG2	liver
18	chr1:155025400-155028800	Weak transcription	Brain Germinal Matrix	brain
19	chr1:155025400-155029000	Weak transcription	Fetal Brain Female	brain
20	chr1:155025400-155034000	Weak transcription	GM12878-XiMat	blood
21	chr1:155025600-155028200	Weak transcription	H9 Cell Line	embryonic stem cell
22	chr1:155025600-155028200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
23	chr1:155025600-155028200	Weak transcription	Muscle Satellite Cultured Cells	--
24	chr1:155025600-155028600	Weak transcription	HUES48 Cell Line	embryonic stem cell
25	chr1:155025600-155028600	Weak transcription	Stomach Mucosa	stomach
26	chr1:155025600-155030400	Weak transcription	HUES64 Cell Line	embryonic stem cell
27	chr1:155025600-155033800	Weak transcription	H1 Cell Line	embryonic stem cell
28	chr1:155025600-155034200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
29	chr1:155025800-155027000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
30	chr1:155025800-155028200	Weak transcription	HSMM	muscle
31	chr1:155025800-155028400	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
32	chr1:155025800-155031400	Strong transcription	Fetal Intestine Small	intestine
33	chr1:155025800-155031800	Strong transcription	Brain Inferior Temporal Lobe	brain
34	chr1:155025800-155033600	Strong transcription	A549	lung
35	chr1:155025800-155034000	Strong transcription	Brain Cingulate Gyrus	brain
36	chr1:155026000-155027000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
37	chr1:155026000-155028200	Weak transcription	Primary T cells from cord blood	blood
38	chr1:155026000-155028200	Weak transcription	Colonic Mucosa	Colon
39	chr1:155026000-155028200	Weak transcription	Fetal Intestine Large	intestine
40	chr1:155026000-155028400	Weak transcription	Primary T cells fromperipheralblood	blood
41	chr1:155026000-155029400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
42	chr1:155026000-155030800	Weak transcription	K562	blood
43	chr1:155026000-155033200	Strong transcription	Brain Dorsolateral Prefrontal Cortex	brain
44	chr1:155026000-155033600	Strong transcription	Brain Substantia Nigra	brain
45	chr1:155026000-155033800	Weak transcription	Primary T helper cells PMA-I stimulated	--
46	chr1:155026000-155033800	Strong transcription	Fetal Stomach	stomach
47	chr1:155026000-155034200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
48	chr1:155026000-155034200	Weak transcription	Right Atrium	heart
49	chr1:155026200-155027800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
50	chr1:155026200-155029200	Strong transcription	Right Ventricle	heart

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