Variant report

Variant	nsv998933
Chromosome Location	chr1:227992928-228059296
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:415)
CpG islands
(count:550)
Chromatin interactive
region (count:20)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:415 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

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	chr1:228034164-228034420	K562	blood:	n/a	n/a
9	BHLHE40	chr1:228036186-228036675	K562	blood:	n/a	n/a
10	BRCA1	chr1:227993242-227993704	Hela-S3	cervix:	n/a	n/a
11	CBX3	chr1:228003121-228003526	K562	blood:	n/a	n/a
12	CBX3	chr1:227993189-227994028	HCT-116	colon:	n/a	n/a
13	CBX3	chr1:228001542-228002075	K562	blood:	n/a	n/a
14	CBX3	chr1:227993132-227994273	HCT-116	colon:	n/a	n/a
15	CBX3	chr1:228001453-228002244	K562	blood:	n/a	n/a
16	CCNT2	chr1:228036153-228036521	K562	blood:	n/a	n/a
17	CEBPB	chr1:228036106-228036736	K562	blood:	n/a	n/a
18	CEBPB	chr1:228000148-228000228	HepG2	liver:	n/a	chr1:228000177-228000188
19	CEBPB	chr1:228045316-228045525	A549	lung:	n/a	n/a
20	CEBPB	chr1:228045134-228045555	K562	blood:	n/a	n/a
21	CEBPB	chr1:228039485-228039493	K562	blood:	n/a	n/a
22	CEBPB	chr1:228011241-228011442	K562	blood:	n/a	chr1:228011381-228011392
23	CEBPB	chr1:228011291-228011552	Hela-S3	cervix:	n/a	chr1:228011381-228011392
24	CEBPB	chr1:228028775-228028831	K562	blood:	n/a	n/a
25	CEBPB	chr1:228011347-228011422	HepG2	liver:	n/a	chr1:228011381-228011392
26	CEBPB	chr1:228045327-228045529	K562	blood:	n/a	n/a
27	CEBPB	chr1:228045338-228045623	K562	blood:	n/a	n/a
28	CEBPB	chr1:228036187-228036717	K562	blood:	n/a	n/a
29	CEBPB	chr1:228045342-228045543	HepG2	liver:	n/a	n/a
30	CEBPB	chr1:228045459-228045528	IMR90	lung:	n/a	n/a
31	CEBPD	chr1:228036108-228036766	K562	blood:	n/a	n/a
32	CEBPD	chr1:228036132-228036659	K562	blood:	n/a	n/a
33	CHD2	chr1:227993361-227993823	Hela-S3	cervix:	n/a	n/a
34	CHD2	chr1:228036122-228036399	K562	blood:	n/a	n/a
35	CTCF	chr1:227993320-227993470	HEEpiC	esophagus:	n/a	n/a
36	CTCF	chr1:228033060-228033210	HepG2	liver:	n/a	n/a
37	CTCF	chr1:228003260-228003410	HEK293	kidney:	n/a	chr1:228003391-228003404
38	CTCF	chr1:228045811-228045900	MCF-7	breast:	n/a	n/a
39	CTCF	chr1:228003201-228003555	K562	blood:	n/a	chr1:228003391-228003404
40	CTCF	chr1:227993360-227993510	AG09319	gingival:	n/a	n/a
41	CTCF	chr1:228045740-228045890	Hela-S3	cervix:	n/a	n/a
42	CTCF	chr1:228003244-228003465	K562	blood:	n/a	chr1:228003391-228003404
43	CTCF	chr1:228047160-228047310	HEK293	kidney:	n/a	n/a
44	CTCF	chr1:228003252-228003443	HepG2	liver:	n/a	chr1:228003391-228003404
45	CTCF	chr1:227993360-227993510	HAc	cerebellar:	n/a	n/a
46	CTCF	chr1:228033000-228033150	K562	blood:	n/a	n/a
47	CTCF	chr1:227993320-227993470	HMEC	breast:	n/a	n/a
48	CTCF	chr1:228003222-228003427	MCF-7	breast:	n/a	chr1:228003391-228003404
49	CTCF	chr1:228036920-228037300	K562	blood:	n/a	n/a
50	CTCF	chr1:227993400-227993550	HMF	breast:	n/a	n/a

(count:550 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:228003072-228003122	CMK	blood:	n/a
2	chr1:228003072-228003122	CMK	blood:	n/a
3	chr1:228003072-228003122	GM12892	blood:	n/a
4	chr1:228003072-228003122	T-47D	breast:	n/a
5	chr1:228003900-228003950	HCT-116	colon:	n/a
6	chr1:228004967-228005017	LNCaP	prostate:	n/a
7	chr1:228003900-228003950	K562	blood:	n/a
8	chr1:228003393-228003443	HCT-116	colon:	n/a
9	chr1:228003402-228003452	HCT-116	colon:	n/a
10	chr1:228003393-228003443	NHBE	bronchial:	n/a
11	chr1:228004967-228005017	GM12892	blood:	n/a
12	chr1:228003402-228003452	GM12892	blood:	n/a
13	chr1:228001655-228001705	H1-hESC	embryonic stem cell:	embryo
14	chr1:228003402-228003452	NH-A	brain:	n/a
15	chr1:228003435-228003485	GM12878	blood:	n/a
16	chr1:228003900-228003950	H1-hESC	embryonic stem cell:	embryo
17	chr1:228003072-228003122	K562	blood:	n/a
18	chr1:228003072-228003122	SAEC	small airway:	n/a
19	chr1:228004075-228004125	HCF	heart:	n/a
20	chr1:228004967-228005017	SAEC	small airway:	n/a
21	chr1:228003393-228003443	SAEC	small airway:	n/a
22	chr1:228004075-228004125	HRCEpiC	kidney:	n/a
23	chr1:228003072-228003122	Jurkat	blood:	n/a
24	chr1:228003938-228003988	HIPEpiC	eye:	n/a
25	chr1:228003435-228003485	HepG2	liver:	n/a
26	chr1:228004075-228004125	AG10803	skin:	n/a
27	chr1:228001655-228001705	NHDF-neo	bronchial:	n/a
28	chr1:228003393-228003443	NT2-D1	testis:	n/a
29	chr1:228001655-228001705	GM12892	blood:	n/a
30	chr1:228003435-228003485	HNPCEpiC	eye:	n/a
31	chr1:228004075-228004125	ProgFib	skin:	n/a
32	chr1:228003900-228003950	NH-A	brain:	n/a
33	chr1:228001655-228001705	SAEC	small airway:	n/a
34	chr1:228003938-228003988	HMEC	breast:	n/a
35	chr1:228004967-228005017	HCPEpiC	choroid plexus:	n/a
36	chr1:228004075-228004125	ECC-1	luminal epithelium:	n/a
37	chr1:228003072-228003122	AG04450	lung:	fetal
38	chr1:228004967-228005017	AG04450	lung:	fetal
39	chr1:228003393-228003443	AG04450	lung:	fetal
40	chr1:228003900-228003950	HCM	heart:	n/a
41	chr1:228004967-228005017	HCT-116	colon:	n/a
42	chr1:228003402-228003452	BJ	skin:	n/a
43	chr1:228003900-228003950	AoSMC	blood vessel:	n/a
44	chr1:228003435-228003485	HCT-116	colon:	n/a
45	chr1:228004075-228004125	LNCaP	prostate:	n/a
46	chr1:228003402-228003452	LNCaP	prostate:	n/a
47	chr1:228003938-228003988	CMK	blood:	n/a
48	chr1:228004075-228004125	MCF-7	breast:	n/a
49	chr1:228004967-228005017	NHDF-neo	bronchial:	n/a
50	chr1:228003900-228003950	HPAEpiC	pulmonary alveolar:	n/a

(count:20 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:228031958..228038374-chr1:228038684..228045094,10	K562	blood:
2	chr1:228032135..228035495-chr1:228035630..228038302,4	MCF-7	breast:
3	chr1:228052542..228054437-chr1:228057265..228059501,2	K562	blood:
4	chr1:228024720..228027679-chr1:228032169..228034658,3	K562	blood:
5	chr1:228043935..228045545-chr1:228052493..228054458,2	K562	blood:
6	chr1:228003528..228005647-chr1:228006569..228009542,2	K562	blood:
7	chr1:228003528..228005647-chr1:228006569..228009542,2	K562	blood:
8	chr1:228032607..228033237-chr1:228089693..228090487,2	MCF-7	breast:
9	chr1:228055780..228058656-chr1:228138484..228140779,2	MCF-7	breast:
10	chr1:228024720..228027679-chr1:228032169..228034658,3	K562	blood:
11	chr1:228020602..228022797-chr1:228027423..228029400,2	K562	blood:
12	chr1:228043935..228045545-chr1:228052493..228054458,2	K562	blood:
13	chr1:227992970..227993567-chr1:228129726..228130492,2	MCF-7	breast:
14	chr1:228031958..228038374-chr1:228038684..228045094,10	K562	blood:
15	chr1:228052542..228054437-chr1:228057265..228059501,2	K562	blood:
16	chr1:228050325..228052632-chr1:228054313..228055923,2	K562	blood:
17	chr1:228050325..228052632-chr1:228054313..228055923,2	K562	blood:
18	chr1:227912232..227914345-chr1:228021397..228023530,2	K562	blood:
19	chr1:228020602..228022797-chr1:228027423..228029400,2	K562	blood:
20	chr1:228032135..228035495-chr1:228035630..228038302,4	MCF-7	breast:

No data

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

Extended variants
information (count: 1600 )
Associated
traits (count: 93 )

Variant overlapped rSNPs/rCNVs (count:1600 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6679942	chr1:227992928-227992929	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs115339804	chr1:227992942-227992943	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs561081249	chr1:227993007-227993008	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs79823524	chr1:227993008-227993009	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs531672747	chr1:227993081-227993082	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs35862668	chr1:227993113-227993114	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs372362962	chr1:227993169-227993170	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs187791705	chr1:227993176-227993177	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs375385000	chr1:227993203-227993204	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs78319112	chr1:227993227-227993228	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs565881721	chr1:227993296-227993297	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs536091923	chr1:227993347-227993348	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs193137037	chr1:227993357-227993358	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs569811126	chr1:227993367-227993368	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs60640499	chr1:227993396-227993397	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs77114944	chr1:227993398-227993399	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs576714731	chr1:227993446-227993447	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
18	rs150600125	chr1:227993455-227993456	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
19	rs555476057	chr1:227993694-227993695	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs371741971	chr1:227993717-227993718	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs554138381	chr1:227993725-227993726	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs183927513	chr1:227993737-227993738	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs542843915	chr1:227993806-227993807	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs138636991	chr1:227993818-227993819	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs188455878	chr1:227993819-227993820	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs191959878	chr1:227993824-227993825	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs565301588	chr1:227993825-227993826	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs375334601	chr1:227993827-227993828	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs12057467	chr1:227993868-227993869	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
30	rs558727068	chr1:227993900-227993901	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs71648439	chr1:227993929-227993930	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs71648440	chr1:227993931-227993932	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs559415238	chr1:227993932-227993933	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs10916213	chr1:227993981-227993982	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs199864422	chr1:227994013-227994014	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs141779683	chr1:227994014-227994015	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs578008505	chr1:227994023-227994024	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs368908646	chr1:227994024-227994025	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs146250415	chr1:227994056-227994057	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs552276753	chr1:227994062-227994063	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs570444255	chr1:227994084-227994085	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs71648441	chr1:227994089-227994090	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs58979934	chr1:227994126-227994127	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs560092824	chr1:227994159-227994160	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs66579310	chr1:227994184-227994185	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs77833864	chr1:227994247-227994248	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs536539608	chr1:227994267-227994268	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs78308842	chr1:227994277-227994278	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs59772405	chr1:227994284-227994285	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs7548859	chr1:227994297-227994298	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:93)

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
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:162 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:227990400-227997800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr1:227992800-227993000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
3	chr1:227993000-227994200	Enhancers	NHEK	skin
4	chr1:227993000-227994400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
5	chr1:227993000-227994400	Enhancers	HMEC	breast
6	chr1:227993200-227994200	Enhancers	NH-A	brain
7	chr1:227993200-227994400	Enhancers	Muscle Satellite Cultured Cells	--
8	chr1:227993200-227994600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr1:227993400-227993600	Bivalent Enhancer	Skeletal Muscle Female	skeletal muscle
10	chr1:227993400-227993800	Enhancers	HSMM	muscle
11	chr1:227993400-227994000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
12	chr1:227993400-227994000	Enhancers	HSMMtube	muscle
13	chr1:227993600-227993800	Enhancers	Skeletal Muscle Female	skeletal muscle
14	chr1:227993600-227994000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
15	chr1:227993600-227994000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr1:227993600-227994000	Enhancers	Colon Smooth Muscle	Colon
17	chr1:227993600-227994000	Enhancers	NHLF	lung
18	chr1:227993600-227994200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr1:227993600-227994400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
20	chr1:227993600-227994400	Enhancers	Hela-S3	cervix
21	chr1:227993600-227994400	Enhancers	Osteobl	bone
22	chr1:227993800-227994000	Weak transcription	HSMM	muscle
23	chr1:227994000-227994400	Enhancers	HSMM	muscle
24	chr1:227994400-227994600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
25	chr1:227994400-227996000	Weak transcription	HMEC	breast
26	chr1:227994400-227996200	Weak transcription	Muscle Satellite Cultured Cells	--
27	chr1:227995800-227996600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
28	chr1:227996000-227996600	Enhancers	HMEC	breast
29	chr1:227996200-227996800	Enhancers	Muscle Satellite Cultured Cells	--
30	chr1:227996400-227996600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
31	chr1:227996400-227996600	Enhancers	HSMM	muscle
32	chr1:227996400-227996800	Enhancers	Primary T helper naive cells from peripheral blood	blood
33	chr1:227996400-227996800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
34	chr1:227996400-227996800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
35	chr1:227996400-227996800	Enhancers	Primary T helper cells fromperipheralblood	blood
36	chr1:227996400-227997000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
37	chr1:227996400-227997000	Enhancers	Primary T helper cells PMA-I stimulated	--
38	chr1:228001400-228002000	ZNF genes & repeats	Brain Dorsolateral Prefrontal Cortex	brain
39	chr1:228003200-228005000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr1:228003800-228005400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
41	chr1:228004200-228005400	Enhancers	Primary T cells fromperipheralblood	blood
42	chr1:228004600-228005000	Enhancers	Primary hematopoietic stem cells short term culture	blood
43	chr1:228004600-228005200	Enhancers	Primary T killer memory cells from peripheral blood	blood
44	chr1:228004600-228005400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
45	chr1:228005000-228005200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
46	chr1:228014800-228015000	Enhancers	Primary T helper naive cells from peripheral blood	blood
47	chr1:228014800-228016800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
48	chr1:228015000-228015800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
49	chr1:228015000-228016800	Enhancers	Primary T killer memory cells from peripheral blood	blood
50	chr1:228015800-228017000	Enhancers	Primary T helper naive cells from peripheral blood	blood

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