Variant report

Variant	esv3384525
Chromosome Location	chr1:155234828-155239426
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:61)
CpG islands
(count:245)
Chromatin interactive
region (count:13)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:61 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CTCF	chr1:155235400-155235550	HepG2	liver:	n/a	n/a
2	CTCF	chr1:155237660-155237810	HepG2	liver:	n/a	n/a
3	MYC	chr1:155238851-155238876	HUVEC	blood vessel:	n/a	n/a
4	POLR2A	chr1:155236042-155236781	K562	blood:	n/a	n/a
5	POLR2A	chr1:155235894-155236740	PFSK-1	brain:	n/a	n/a
6	POLR2A	chr1:155237110-155237579	PFSK-1	brain:	n/a	n/a
7	POLR2A	chr1:155236559-155236891	K562	blood:	n/a	n/a
8	POLR2A	chr1:155235073-155235109	HUVEC	blood vessel:	n/a	n/a
9	POLR2A	chr1:155239296-155239533	Hela-S3	cervix:	n/a	n/a
10	POLR2A	chr1:155236218-155236854	GM12892	blood:	n/a	n/a
11	POLR2A	chr1:155238706-155238797	Hela-S3	cervix:	n/a	n/a
12	POLR2A	chr1:155238621-155239115	PFSK-1	brain:	n/a	n/a
13	POLR2A	chr1:155237186-155238589	HepG2	liver:	n/a	n/a
14	POLR2A	chr1:155236448-155236704	Hela-S3	cervix:	n/a	n/a
15	POLR2A	chr1:155235678-155236144	K562	blood:	n/a	n/a
16	POLR2A	chr1:155235802-155235809	MCF-7	breast:	n/a	n/a
17	POLR2A	chr1:155235680-155235792	MCF-7	breast:	n/a	n/a
18	POLR2A	chr1:155236470-155236593	H1-hESC	embryonic stem cell:	n/a	n/a
19	POLR2A	chr1:155234875-155234969	HepG2	liver:	n/a	n/a
20	POLR2A	chr1:155235653-155235850	H1-hESC	embryonic stem cell:	n/a	n/a
21	POLR2A	chr1:155239255-155239576	H1-hESC	embryonic stem cell:	n/a	n/a
22	POLR2A	chr1:155239268-155239283	K562	blood:	n/a	n/a
23	POLR2A	chr1:155235398-155236778	SK-N-MC	brain:	n/a	n/a
24	POLR2A	chr1:155236339-155236857	K562	blood:	n/a	n/a
25	POLR2A	chr1:155235561-155235895	GM12892	blood:	n/a	n/a
26	POLR2A	chr1:155235639-155235762	Hela-S3	cervix:	n/a	n/a
27	POLR2A	chr1:155239397-155239659	K562	blood:	n/a	n/a
28	POLR2A	chr1:155235018-155235338	HepG2	liver:	n/a	n/a
29	POLR2A	chr1:155239124-155239549	K562	blood:	n/a	n/a
30	POLR2A	chr1:155239124-155239743	HepG2	liver:	n/a	n/a
31	POLR2A	chr1:155239117-155239119	HepG2	liver:	n/a	n/a
32	POLR2A	chr1:155238207-155238349	K562	blood:	n/a	n/a
33	POLR2A	chr1:155234857-155234864	HepG2	liver:	n/a	n/a
34	POLR2A	chr1:155236360-155236806	K562	blood:	n/a	n/a
35	POLR2A	chr1:155230931-155235183	PFSK-1	brain:	n/a	n/a
36	POLR2A	chr1:155238594-155239040	HepG2	liver:	n/a	n/a
37	POLR2A	chr1:155235706-155235938	K562	blood:	n/a	n/a
38	POLR2A	chr1:155238370-155238374	K562	blood:	n/a	n/a
39	POLR2A	chr1:155238965-155238970	GM12878	blood:	n/a	n/a
40	POLR2A	chr1:155236248-155236264	K562	blood:	n/a	n/a
41	POLR2A	chr1:155231107-155235305	SK-N-MC	brain:	n/a	n/a
42	POLR2A	chr1:155239315-155239336	K562	blood:	n/a	n/a
43	POLR2A	chr1:155235668-155235822	HUVEC	blood vessel:	n/a	n/a
44	POLR2A	chr1:155236163-155236245	K562	blood:	n/a	n/a
45	POLR2A	chr1:155235524-155237148	HepG2	liver:	n/a	n/a
46	POLR2A	chr1:155235600-155235669	K562	blood:	n/a	n/a
47	POLR2A	chr1:155239295-155239307	K562	blood:	n/a	n/a
48	POLR2A	chr1:155238427-155238453	Hela-S3	cervix:	n/a	n/a
49	POLR2A	chr1:155239181-155239714	PFSK-1	brain:	n/a	n/a
50	POLR2A	chr1:155235648-155236809	HepG2	liver:	n/a	n/a

(count:245 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:155238752-155238802	HNPCEpiC	eye:	n/a
2	chr1:155238752-155238802	HNPCEpiC	eye:	n/a
3	chr1:155236380-155236430	HNPCEpiC	eye:	n/a
4	chr1:155239301-155239351	GM12892	blood:	n/a
5	chr1:155239421-155239471	IMR90	lung:	fetal
6	chr1:155236380-155236430	ProgFib	skin:	n/a
7	chr1:155236380-155236430	GM19239	blood:	n/a
8	chr1:155239421-155239471	NHBE	bronchial:	n/a
9	chr1:155236380-155236430	SKMC	muscle:	n/a
10	chr1:155236380-155236430	HepG2	liver:	n/a
11	chr1:155239421-155239471	ovcar-3	ovarian:	n/a
12	chr1:155236380-155236430	PANC-1	pancreas:	n/a
13	chr1:155238752-155238802	MCF10A-Er-Src	breast:	n/a
14	chr1:155239301-155239351	MCF-7	breast:	n/a
15	chr1:155239421-155239471	SK-N-SH	brain:	n/a
16	chr1:155239421-155239471	H1-hESC	embryonic stem cell:	embryo
17	chr1:155238752-155238802	GM12891	blood:	n/a
18	chr1:155239301-155239351	HUVEC	blood vessel:	n/a
19	chr1:155239301-155239351	NT2-D1	testis:	n/a
20	chr1:155239301-155239351	BJ	skin:	n/a
21	chr1:155239301-155239351	IMR90	lung:	fetal
22	chr1:155236380-155236430	HRCEpiC	kidney:	n/a
23	chr1:155239421-155239471	PrEC	prostate:	n/a
24	chr1:155238752-155238802	HepG2	liver:	n/a
25	chr1:155236380-155236430	U87	brain:	n/a
26	chr1:155239421-155239471	MCF-7	breast:	n/a
27	chr1:155239421-155239471	GM12878	blood:	n/a
28	chr1:155239421-155239471	Hepatocyte	liver:	n/a
29	chr1:155236380-155236430	BE2_C	brain:	n/a
30	chr1:155236380-155236430	PrEC	prostate:	n/a
31	chr1:155238752-155238802	SK-N-SH_RA	brain:	n/a
32	chr1:155239421-155239471	BE2_C	brain:	n/a
33	chr1:155239301-155239351	HCM	heart:	n/a
34	chr1:155236380-155236430	AG10803	skin:	n/a
35	chr1:155239421-155239471	HNPCEpiC	eye:	n/a
36	chr1:155239421-155239471	CMK	blood:	n/a
37	chr1:155238752-155238802	BJ	skin:	n/a
38	chr1:155236380-155236430	HIPEpiC	eye:	n/a
39	chr1:155236380-155236430	HEK293	kidney:	embryo
40	chr1:155239301-155239351	SKMC	muscle:	n/a
41	chr1:155236380-155236430	ovcar-3	ovarian:	n/a
42	chr1:155239301-155239351	HCT-116	colon:	n/a
43	chr1:155236380-155236430	AoSMC	blood vessel:	n/a
44	chr1:155239421-155239471	K562	blood:	n/a
45	chr1:155239421-155239471	HCT-116	colon:	n/a
46	chr1:155239301-155239351	Hepatocyte	liver:	n/a
47	chr1:155238752-155238802	NHDF-neo	bronchial:	n/a
48	chr1:155239301-155239351	HIPEpiC	eye:	n/a
49	chr1:155239421-155239471	PFSK-1	brain:	n/a
50	chr1:155238752-155238802	AG04450	lung:	fetal

(count:13 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:155234973..155237775-chr1:155290971..155293651,2	MCF-7	breast:
2	chr1:155239314..155245036-chr1:155288379..155297041,21	MCF-7	breast:
3	chr1:155218456..155235751-chr1:155288837..155299195,44	MCF-7	breast:
4	chr1:155174569..155177437-chr1:155233735..155235626,3	K562	blood:
5	chr1:155237070..155244636-chr1:155291827..155295779,11	K562	blood:
6	chr1:155214449..155216184-chr1:155237561..155239532,2	MCF-7	breast:
7	chr1:155211690..155216212-chr1:155231766..155235735,5	MCF-7	breast:
8	chr1:155238212..155240823-chr1:155276858..155278738,2	K562	blood:
9	chr1:155234574..155237301-chr17:58677118..58679465,2	MCF-7	breast:
10	chr1:155229082..155234937-chr1:155291248..155296864,8	K562	blood:
11	chr1:155235972..155238803-chr1:155277477..155279791,2	MCF-7	breast:
12	chr1:155236269..155241954-chr1:155291931..155295779,5	K562	blood:
13	chr1:155167345..155170267-chr1:155238790..155240384,2	MCF-7	breast:

No data

Variant related genes	Relation type
SCAMP3	TF binding region
CLK2	TF binding region
SCAMP3	CpG island
CLK2	CpG island
ENSG00000170836	chromatin interactions
ENSG00000231064	chromatin interactions
ENSG00000177628	chromatin interactions
ENSG00000160753	chromatin interactions
ENSG00000160752	chromatin interactions
ENSG00000169231	chromatin interactions
ENSG00000225855	chromatin interactions

Extended variants
information (count: 186 )
Associated
traits (count: 101 )

Variant overlapped rSNPs/rCNVs (count:186 , 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	rs199775545	chr1:155234828-155234829	Strong transcription Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
2	rs12044394	chr1:155234895-155234896	Strong transcription Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
3	rs12043655	chr1:155234911-155234912	Strong transcription Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
4	rs148772014	chr1:155234914-155234915	Strong transcription Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
5	rs142437332	chr1:155234975-155234976	Strong transcription Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
6	rs760081	chr1:155235002-155235003	Strong transcription Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
7	rs560934907	chr1:155235003-155235004	Strong transcription Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
8	rs371662792	chr1:155235072-155235073	Strong transcription Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
9	rs528114726	chr1:155235123-155235124	Strong transcription Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
10	rs546653624	chr1:155235126-155235127	Strong transcription Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
11	rs7355033	chr1:155235140-155235141	Strong transcription Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
12	rs371474130	chr1:155235143-155235144	Strong transcription Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
13	rs540347698	chr1:155235165-155235166	Strong transcription Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
14	rs183533482	chr1:155235168-155235169	Strong transcription Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
15	rs2008420	chr1:155235239-155235240	Strong transcription Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
16	rs538814162	chr1:155235280-155235281	Strong transcription Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
17	rs550771719	chr1:155235310-155235311	Strong transcription Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
18	rs374400975	chr1:155235357-155235358	Strong transcription Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
19	rs569163617	chr1:155235379-155235380	Strong transcription Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
20	rs145986141	chr1:155235383-155235384	Strong transcription Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
21	rs71677925	chr1:155235384-155235385	Strong transcription Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
22	rs200772258	chr1:155235390-155235391	Strong transcription Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
23	rs202113378	chr1:155235391-155235392	Strong transcription Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
24	rs78968000	chr1:155235396-155235397	Strong transcription Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
25	rs555006098	chr1:155235397-155235398	Strong transcription Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
26	rs2008404	chr1:155235398-155235399	Strong transcription Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
27	rs573177018	chr1:155235400-155235401	Strong transcription Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
28	rs188781772	chr1:155235434-155235435	Strong transcription Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
29	rs376387210	chr1:155235484-155235485	Strong transcription Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
30	rs1078699	chr1:155235493-155235494	Strong transcription Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
31	rs760078	chr1:155235535-155235536	Strong transcription Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
32	rs192046581	chr1:155235557-155235558	Strong transcription Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
33	rs182694099	chr1:155235564-155235565	Strong transcription Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
34	rs186829293	chr1:155235586-155235587	Strong transcription Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
35	rs373891454	chr1:155235614-155235615	Strong transcription Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
36	rs528060965	chr1:155235616-155235617	Strong transcription Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
37	rs530384402	chr1:155235622-155235623	Strong transcription Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
38	rs546295338	chr1:155235671-155235672	Strong transcription Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
39	rs147653486	chr1:155235711-155235712	Strong transcription Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
40	rs201747409	chr1:155235753-155235754	Strong transcription Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs542267999	chr1:155235808-155235809	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs2974936	chr1:155235876-155235877	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs116823996	chr1:155235924-155235925	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs6696982	chr1:155235925-155235926	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs143421472	chr1:155235956-155235957	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs11389873	chr1:155235957-155235958	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs376720729	chr1:155235968-155235969	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs184305943	chr1:155235976-155235977	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
49	rs548840427	chr1:155235987-155235988	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
50	rs528072900	chr1:155235991-155235992	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:101)

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
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	22522925	CNVD

Chromatin state (count:177 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:155232000-155242400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr1:155232200-155236400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr1:155232200-155242200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr1:155232400-155241000	Strong transcription	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr1:155232400-155241600	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr1:155232600-155235000	Strong transcription	Foreskin Melanocyte Primary Cells skin01	Skin
7	chr1:155232600-155236200	Weak transcription	Pancreatic Islets	Pancreatic Islet
8	chr1:155232600-155240600	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr1:155232600-155240600	Strong transcription	Primary T killer memory cells from peripheral blood	blood
10	chr1:155232600-155240800	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr1:155232600-155240800	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
12	chr1:155232600-155240800	Strong transcription	Gastric	stomach
13	chr1:155232600-155241000	Strong transcription	HMEC	breast
14	chr1:155232600-155241200	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr1:155232600-155241400	Strong transcription	H1 Cell Line	embryonic stem cell
16	chr1:155232600-155241400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
17	chr1:155232600-155241400	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
18	chr1:155232600-155241600	Strong transcription	HUES48 Cell Line	embryonic stem cell
19	chr1:155232600-155241600	Strong transcription	Primary hematopoietic stem cells short term culture	blood
20	chr1:155232600-155241600	Strong transcription	Fetal Thymus	thymus
21	chr1:155232600-155241600	Strong transcription	Osteobl	bone
22	chr1:155232600-155241800	Strong transcription	ES-I3 Cell Line	embryonic stem cell
23	chr1:155232600-155241800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
24	chr1:155232600-155241800	Strong transcription	HUES6 Cell Line	embryonic stem cell
25	chr1:155232600-155241800	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
26	chr1:155232600-155241800	Strong transcription	Fetal Muscle Trunk	muscle
27	chr1:155232600-155242000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr1:155232600-155242000	Strong transcription	iPS-20b Cell Line	embryonic stem cell
29	chr1:155232600-155242200	Weak transcription	Right Atrium	heart
30	chr1:155232800-155236200	Weak transcription	Fetal Heart	heart
31	chr1:155232800-155236600	Strong transcription	Skeletal Muscle Male	skeletal muscle
32	chr1:155232800-155237800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
33	chr1:155232800-155237800	Weak transcription	Stomach Mucosa	stomach
34	chr1:155232800-155240000	Strong transcription	Primary T helper naive cells from peripheral blood	blood
35	chr1:155232800-155240400	Strong transcription	GM12878-XiMat	blood
36	chr1:155232800-155240600	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
37	chr1:155232800-155240600	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
38	chr1:155232800-155240600	Strong transcription	Primary T helper cells fromperipheralblood	blood
39	chr1:155232800-155240600	Strong transcription	Brain Germinal Matrix	brain
40	chr1:155232800-155240800	Strong transcription	Primary T helper cells PMA-I stimulated	--
41	chr1:155232800-155240800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr1:155232800-155240800	Strong transcription	Fetal Intestine Large	intestine
43	chr1:155232800-155240800	Strong transcription	Thymus	Thymus
44	chr1:155232800-155240800	Strong transcription	HepG2	liver
45	chr1:155232800-155241000	Strong transcription	Primary neutrophils fromperipheralblood	blood
46	chr1:155232800-155241000	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
47	chr1:155232800-155241000	Strong transcription	Adipose Nuclei	Adipose
48	chr1:155232800-155241000	Strong transcription	Liver	Liver
49	chr1:155232800-155241000	Strong transcription	Fetal Brain Female	brain
50	chr1:155232800-155241000	Strong transcription	Fetal Intestine Small	intestine

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