Variant report

Variant	nsv549273
Chromosome Location	chr1:227995966-228051234
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:299)
CpG islands
(count:551)
Chromatin interactive
region (count:14)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:299 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:228035899-228036543	K562	blood:	n/a	n/a
2	ATF1	chr1:228034220-228034459	K562	blood:	n/a	n/a
3	ATF1	chr1:228037033-228037040	K562	blood:	n/a	n/a
4	ATF1	chr1:228036029-228036515	K562	blood:	n/a	n/a
5	ATF3	chr1:228003217-228003449	K562	blood:	n/a	n/a
6	BACH1	chr1:227996473-227996564	K562	blood:	n/a	n/a
7	BACH1	chr1:228036213-228036600	K562	blood:	n/a	n/a
8	BHLHE40	chr1:228036186-228036675	K562	blood:	n/a	n/a
9	BHLHE40	chr1:228034164-228034420	K562	blood:	n/a	n/a
10	CBX3	chr1:228003121-228003526	K562	blood:	n/a	n/a
11	CBX3	chr1:228001453-228002244	K562	blood:	n/a	n/a
12	CBX3	chr1:228001542-228002075	K562	blood:	n/a	n/a
13	CCNT2	chr1:228036153-228036521	K562	blood:	n/a	n/a
14	CEBPB	chr1:228045134-228045555	K562	blood:	n/a	n/a
15	CEBPB	chr1:228036106-228036736	K562	blood:	n/a	n/a
16	CEBPB	chr1:228039485-228039493	K562	blood:	n/a	n/a
17	CEBPB	chr1:228000148-228000228	HepG2	liver:	n/a	chr1:228000177-228000188
18	CEBPB	chr1:228028775-228028831	K562	blood:	n/a	n/a
19	CEBPB	chr1:228045342-228045543	HepG2	liver:	n/a	n/a
20	CEBPB	chr1:228011241-228011442	K562	blood:	n/a	chr1:228011381-228011392
21	CEBPB	chr1:228011347-228011422	HepG2	liver:	n/a	chr1:228011381-228011392
22	CEBPB	chr1:228011291-228011552	Hela-S3	cervix:	n/a	chr1:228011381-228011392
23	CEBPB	chr1:228045316-228045525	A549	lung:	n/a	n/a
24	CEBPB	chr1:228045327-228045529	K562	blood:	n/a	n/a
25	CEBPB	chr1:228045338-228045623	K562	blood:	n/a	n/a
26	CEBPB	chr1:228045459-228045528	IMR90	lung:	n/a	n/a
27	CEBPB	chr1:228036187-228036717	K562	blood:	n/a	n/a
28	CEBPD	chr1:228036108-228036766	K562	blood:	n/a	n/a
29	CEBPD	chr1:228036132-228036659	K562	blood:	n/a	n/a
30	CHD2	chr1:228036122-228036399	K562	blood:	n/a	n/a
31	CTCF	chr1:228003219-228003373	Gliobla	brain:	n/a	n/a
32	CTCF	chr1:228003230-228003338	Fibrobl	skin:	n/a	n/a
33	CTCF	chr1:228003137-228003520	H1-hESC	embryonic stem cell:	n/a	chr1:228003391-228003404
34	CTCF	chr1:228003073-228003568	K562	blood:	n/a	chr1:228003391-228003404
35	CTCF	chr1:228003240-228003390	HepG2	liver:	n/a	n/a
36	CTCF	chr1:228045820-228045875	MCF-7	breast:	n/a	n/a
37	CTCF	chr1:228047160-228047310	HEK293	kidney:	n/a	n/a
38	CTCF	chr1:228045740-228045890	Hela-S3	cervix:	n/a	n/a
39	CTCF	chr1:228046600-228046750	GM12872	blood:	n/a	n/a
40	CTCF	chr1:228003320-228003470	K562	blood:	n/a	chr1:228003391-228003404
41	CTCF	chr1:228037062-228037184	K562	blood:	n/a	n/a
42	CTCF	chr1:228003360-228003510	A549	lung:	n/a	chr1:228003391-228003404
43	CTCF	chr1:228003180-228003471	H1-hESC	embryonic stem cell:	n/a	chr1:228003391-228003404
44	CTCF	chr1:228003231-228003338	A549	lung:	n/a	n/a
45	CTCF	chr1:228003140-228003290	HAc	cerebellar:	n/a	n/a
46	CTCF	chr1:228003240-228003390	Hela-S3	cervix:	n/a	n/a
47	CTCF	chr1:228003240-228003390	GM12872	blood:	n/a	n/a
48	CTCF	chr1:228045808-228045854	MCF-7	breast:	n/a	n/a
49	CTCF	chr1:228047120-228047270	Hela-S3	cervix:	n/a	n/a
50	CTCF	chr1:228003244-228003465	K562	blood:	n/a	chr1:228003391-228003404

(count:551 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:228003072-228003122	SK-N-SH	brain:	n/a
2	chr1:228001655-228001705	A549	lung:	n/a
3	chr1:228003072-228003122	SK-N-SH	brain:	n/a
4	chr1:228001655-228001705	A549	lung:	n/a
5	chr1:228003402-228003452	NHDF-neo	bronchial:	n/a
6	chr1:228003435-228003485	GM19239	blood:	n/a
7	chr1:228004967-228005017	SK-N-SH_RA	brain:	n/a
8	chr1:228001655-228001705	GM12891	blood:	n/a
9	chr1:228003938-228003988	AG10803	skin:	n/a
10	chr1:228003072-228003122	HUVEC	blood vessel:	n/a
11	chr1:228003393-228003443	HPAEpiC	pulmonary alveolar:	n/a
12	chr1:228003393-228003443	HRE	kidney:	n/a
13	chr1:228003072-228003122	HIPEpiC	eye:	n/a
14	chr1:228003900-228003950	PrEC	prostate:	n/a
15	chr1:228003402-228003452	SAEC	small airway:	n/a
16	chr1:228003900-228003950	HPAEpiC	pulmonary alveolar:	n/a
17	chr1:228004967-228005017	MCF10A-Er-Src	breast:	n/a
18	chr1:228001655-228001705	NHDF-neo	bronchial:	n/a
19	chr1:228003900-228003950	HepG2	liver:	n/a
20	chr1:228003072-228003122	NH-A	brain:	n/a
21	chr1:228003072-228003122	MCF10A-Er-Src	breast:	n/a
22	chr1:228004967-228005017	HepG2	liver:	n/a
23	chr1:228003938-228003988	T-47D	breast:	n/a
24	chr1:228003435-228003485	HUVEC	blood vessel:	n/a
25	chr1:228001655-228001705	PANC-1	pancreas:	n/a
26	chr1:228004967-228005017	AG04449	skin:	fetal
27	chr1:228001655-228001705	AG09309	skin:	n/a
28	chr1:228003900-228003950	HUVEC	blood vessel:	n/a
29	chr1:228003435-228003485	HCF	heart:	n/a
30	chr1:228003402-228003452	A549	lung:	n/a
31	chr1:228001655-228001705	PrEC	prostate:	n/a
32	chr1:228003072-228003122	Hela-S3	cervix:	n/a
33	chr1:228003393-228003443	GM12891	blood:	n/a
34	chr1:228003435-228003485	HEK293	kidney:	embryo
35	chr1:228003435-228003485	SK-N-MC	brain:	n/a
36	chr1:228003402-228003452	HRCEpiC	kidney:	n/a
37	chr1:228003393-228003443	HIPEpiC	eye:	n/a
38	chr1:228003900-228003950	RPTEC	kidney:	n/a
39	chr1:228003393-228003443	AG04450	lung:	fetal
40	chr1:228003402-228003452	BJ	skin:	n/a
41	chr1:228003900-228003950	Hepatocyte	liver:	n/a
42	chr1:228004075-228004125	GM06990	blood:	n/a
43	chr1:228003938-228003988	HEEpiC	esophagus:	n/a
44	chr1:228001655-228001705	Hela-S3	cervix:	n/a
45	chr1:228004075-228004125	BJ	skin:	n/a
46	chr1:228003072-228003122	HMEC	breast:	n/a
47	chr1:228003435-228003485	PrEC	prostate:	n/a
48	chr1:228003072-228003122	GM12891	blood:	n/a
49	chr1:228003072-228003122	GM12892	blood:	n/a
50	chr1:228003938-228003988	HIPEpiC	eye:	n/a

(count:14 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:228003528..228005647-chr1:228006569..228009542,2	K562	blood:
2	chr1:228020602..228022797-chr1:228027423..228029400,2	K562	blood:
3	chr1:228024720..228027679-chr1:228032169..228034658,3	K562	blood:
4	chr1:228050325..228052632-chr1:228054313..228055923,2	K562	blood:
5	chr1:228031958..228038374-chr1:228038684..228045094,10	K562	blood:
6	chr1:228032135..228035495-chr1:228035630..228038302,4	MCF-7	breast:
7	chr1:228020602..228022797-chr1:228027423..228029400,2	K562	blood:
8	chr1:228031958..228038374-chr1:228038684..228045094,10	K562	blood:
9	chr1:228024720..228027679-chr1:228032169..228034658,3	K562	blood:
10	chr1:228003528..228005647-chr1:228006569..228009542,2	K562	blood:
11	chr1:228032135..228035495-chr1:228035630..228038302,4	MCF-7	breast:
12	chr1:228032607..228033237-chr1:228089693..228090487,2	MCF-7	breast:
13	chr1:227912232..227914345-chr1:228021397..228023530,2	K562	blood:
14	chr1:228043935..228045545-chr1:228052493..228054458,2	K562	blood:

No data

Variant related genes	Relation type
PRSS38	TF binding region
PRSS38	CpG island

Extended variants
information (count: 1221 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:1221 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4394649	chr1:227995966-227995967	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs561473933	chr1:227995976-227995977	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs528952388	chr1:227995985-227995986	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs6702713	chr1:227996064-227996065	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
5	rs562100572	chr1:227996082-227996083	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs531112281	chr1:227996148-227996149	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs552806216	chr1:227996183-227996184	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs148186894	chr1:227996210-227996211	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs182213321	chr1:227996243-227996244	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs547195827	chr1:227996251-227996252	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs59541986	chr1:227996309-227996310	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs185505723	chr1:227996359-227996360	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs146257631	chr1:227996371-227996372	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs371458880	chr1:227996400-227996401	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs539374356	chr1:227996478-227996479	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs557999465	chr1:227996538-227996539	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs76693327	chr1:227996556-227996557	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs540467140	chr1:227996559-227996560	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs190025539	chr1:227996570-227996571	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs78879596	chr1:227996663-227996664	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs557571964	chr1:227996669-227996670	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs181678391	chr1:227996674-227996675	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs185865443	chr1:227996774-227996775	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs142548210	chr1:227996821-227996822	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs34206017	chr1:227996895-227996896	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs532904909	chr1:227996934-227996935	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs75018471	chr1:227996994-227996995	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs112842195	chr1:227996995-227996996	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs150649824	chr1:227997038-227997039	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs199742031	chr1:227997064-227997065	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs139752834	chr1:227997090-227997091	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs529410268	chr1:227997092-227997093	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs551066659	chr1:227997100-227997101	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs376784952	chr1:227997105-227997106	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs116468434	chr1:227997135-227997136	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs539847538	chr1:227997177-227997178	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs190227023	chr1:227997207-227997208	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs566798112	chr1:227997248-227997249	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs181151730	chr1:227997275-227997276	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs555143141	chr1:227997278-227997279	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs553223214	chr1:227997305-227997306	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs573470401	chr1:227997307-227997308	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs4480354	chr1:227997364-227997365	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs149369661	chr1:227997393-227997394	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs577644548	chr1:227997402-227997403	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs545037968	chr1:227997444-227997445	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs559886668	chr1:227997465-227997466	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs528793660	chr1:227997489-227997490	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs573226850	chr1:227997495-227997496	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs78043846	chr1:227997603-227997604	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:92)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Autism	22495311	CNVD
Melanoma	18172304	CNVD
Rett syndrome	21593744	CNVD
Medulloblastoma	21979893	CNVD
Cancer	20164919	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	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
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Liposarcoma	21253554	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
Breast cancer	17603634	CNVD
Neuroblastoma	21899760	CNVD
Breast cancer	21858162	CNVD
Non-small cell lung cancer	21385341	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Testicular germ cell tumor	18059402	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Breast cancer	21509527	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Chordoma	18071362	CNVD
T-cell lymphomas	19863542	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hepatocellular carcinoma	18803288	CNVD
Urothelial tumor	18831757	CNVD
Lung cancer	18438408	CNVD
Medulloblastoma	16783165	CNVD
Basal cell lymphoma	17170743	CNVD
Mental retardation	19951919	CNVD
Non-syndromic sensorineural hearing loss	17873649	CNVD
Basal cell lymphoma	17053054	CNVD
Autism	14699429	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Fumarase deficiency	21572526	CNVD
Autism	17483303	CNVD
Kartagener syndrome	16639409	CNVD
Congenital abnormalities	21549014	CNVD
Developmental delay	21549014	CNVD
Mental retardation	21549014	CNVD
small cell lung cancer	20016488	CNVD
Glioblastoma multiforme	21138945	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Cancer	20164920	CNVD
Cancer	17060936	CNVD
Myelofibrosis	22110671	CNVD
abnormal development	18461090	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:66 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:227990400-227997800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr1:227994400-227996000	Weak transcription	HMEC	breast
3	chr1:227994400-227996200	Weak transcription	Muscle Satellite Cultured Cells	--
4	chr1:227995800-227996600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr1:227996000-227996600	Enhancers	HMEC	breast
6	chr1:227996200-227996800	Enhancers	Muscle Satellite Cultured Cells	--
7	chr1:227996400-227996600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
8	chr1:227996400-227996600	Enhancers	HSMM	muscle
9	chr1:227996400-227996800	Enhancers	Primary T helper naive cells from peripheral blood	blood
10	chr1:227996400-227996800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
11	chr1:227996400-227996800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
12	chr1:227996400-227996800	Enhancers	Primary T helper cells fromperipheralblood	blood
13	chr1:227996400-227997000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
14	chr1:227996400-227997000	Enhancers	Primary T helper cells PMA-I stimulated	--
15	chr1:228001400-228002000	ZNF genes & repeats	Brain Dorsolateral Prefrontal Cortex	brain
16	chr1:228003200-228005000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr1:228003800-228005400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
18	chr1:228004200-228005400	Enhancers	Primary T cells fromperipheralblood	blood
19	chr1:228004600-228005000	Enhancers	Primary hematopoietic stem cells short term culture	blood
20	chr1:228004600-228005200	Enhancers	Primary T killer memory cells from peripheral blood	blood
21	chr1:228004600-228005400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
22	chr1:228005000-228005200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
23	chr1:228014800-228015000	Enhancers	Primary T helper naive cells from peripheral blood	blood
24	chr1:228014800-228016800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
25	chr1:228015000-228015800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
26	chr1:228015000-228016800	Enhancers	Primary T killer memory cells from peripheral blood	blood
27	chr1:228015800-228017000	Enhancers	Primary T helper naive cells from peripheral blood	blood
28	chr1:228016000-228017000	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
29	chr1:228016200-228016600	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
30	chr1:228016200-228017000	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
31	chr1:228016600-228016800	Bivalent/Poised TSS	Foreskin Melanocyte Primary Cells skin01	Skin
32	chr1:228016600-228017000	Enhancers	Dnd41	blood
33	chr1:228016600-228017000	Enhancers	HMEC	breast
34	chr1:228026000-228026400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
35	chr1:228028800-228029600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
36	chr1:228029000-228029200	Enhancers	K562	blood
37	chr1:228029200-228029400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
38	chr1:228029200-228033200	Weak transcription	K562	blood
39	chr1:228029600-228032000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr1:228031800-228032200	Enhancers	Primary T cells fromperipheralblood	blood
41	chr1:228031800-228032400	Enhancers	Primary T helper cells PMA-I stimulated	--
42	chr1:228031800-228032400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
43	chr1:228032000-228032800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
44	chr1:228032200-228032800	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
45	chr1:228032400-228032800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
46	chr1:228032800-228033200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
47	chr1:228033000-228033600	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
48	chr1:228033200-228034000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
49	chr1:228033200-228035800	Enhancers	K562	blood
50	chr1:228034000-228034400	Enhancers	HSMM	muscle

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