Variant report

Variant	nsv4548
Chromosome Location	chr4:151867014-151908030
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:740)
CpG islands
(count:61)
Chromatin interactive
region (count:22)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:740 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:151868540-151868740	K562	blood:	n/a	n/a
2	ARID3A	chr4:151873740-151874096	K562	blood:	n/a	n/a
3	ARID3A	chr4:151881254-151881563	HepG2	liver:	n/a	n/a
4	ARID3A	chr4:151871889-151872080	K562	blood:	n/a	n/a
5	ARID3A	chr4:151895022-151895519	HepG2	liver:	n/a	n/a
6	ATF1	chr4:151871851-151872033	K562	blood:	n/a	n/a
7	ATF2	chr4:151883309-151883770	GM12878	blood:	n/a	n/a
8	ATF2	chr4:151891943-151892376	GM12878	blood:	n/a	n/a
9	ATF2	chr4:151883376-151883716	GM12878	blood:	n/a	n/a
10	ATF2	chr4:151891901-151892476	GM12878	blood:	n/a	n/a
11	BACH1	chr4:151888580-151888605	H1-hESC	embryonic stem cell:	n/a	n/a
12	BATF	chr4:151891933-151892467	GM12878	blood:	n/a	chr4:151892157-151892168
13	BATF	chr4:151907272-151907595	GM12878	blood:	n/a	n/a
14	BATF	chr4:151883438-151883691	GM12878	blood:	n/a	n/a
15	BATF	chr4:151907232-151907526	GM12878	blood:	n/a	n/a
16	BATF	chr4:151892002-151892355	GM12878	blood:	n/a	chr4:151892157-151892168
17	BCL11A	chr4:151892034-151892342	GM12878	blood:	n/a	n/a
18	BCL3	chr4:151891906-151892317	GM12878	blood:	n/a	n/a
19	BCLAF1	chr4:151883310-151883723	GM12878	blood:	n/a	n/a
20	BCLAF1	chr4:151891977-151892584	GM12878	blood:	n/a	n/a
21	BHLHE40	chr4:151892083-151892335	GM12878	blood:	n/a	n/a
22	BHLHE40	chr4:151871900-151872221	K562	blood:	n/a	n/a
23	BRCA1	chr4:151895398-151895570	HepG2	liver:	n/a	n/a
24	BRCA1	chr4:151896005-151896055	Hela-S3	cervix:	n/a	n/a
25	CBX3	chr4:151900176-151900418	K562	blood:	n/a	n/a
26	CBX3	chr4:151881916-151882345	K562	blood:	n/a	n/a
27	CBX3	chr4:151879093-151879483	K562	blood:	n/a	n/a
28	CBX3	chr4:151897807-151898298	K562	blood:	n/a	n/a
29	CBX3	chr4:151879012-151879707	K562	blood:	n/a	n/a
30	CBX3	chr4:151869866-151870270	K562	blood:	n/a	n/a
31	CBX3	chr4:151871712-151872399	K562	blood:	n/a	n/a
32	CCNT2	chr4:151903848-151904248	K562	blood:	n/a	n/a
33	CEBPB	chr4:151879639-151879809	H1-hESC	embryonic stem cell:	n/a	n/a
34	CEBPB	chr4:151898027-151898372	H1-hESC	embryonic stem cell:	n/a	n/a
35	CEBPB	chr4:151897999-151898085	K562	blood:	n/a	n/a
36	CHD2	chr4:151889585-151889679	Hela-S3	cervix:	n/a	n/a
37	CTCF	chr4:151881360-151881510	Caco-2	colon:	n/a	n/a
38	CTCF	chr4:151881360-151881510	WERI-Rb-1	eye:	n/a	n/a
39	CTCF	chr4:151882060-151882210	HCFaa	heart:	n/a	n/a
40	CTCF	chr4:151882100-151882250	A549	lung:	n/a	n/a
41	CTCF	chr4:151882100-151882250	GM12869	blood:	n/a	n/a
42	CTCF	chr4:151881350-151881518	NHEK	skin:	n/a	n/a
43	CTCF	chr4:151881360-151881510	SAEC	small airway:	n/a	n/a
44	CTCF	chr4:151882079-151882227	LNCaP	prostate:	n/a	n/a
45	CTCF	chr4:151881380-151881530	AG10803	skin:	n/a	n/a
46	CTCF	chr4:151881340-151881490	Caco-2	colon:	n/a	n/a
47	CTCF	chr4:151898102-151898153	MCF-7	breast:	n/a	n/a
48	CTCF	chr4:151881380-151881530	HVMF	connective:	n/a	n/a
49	CTCF	chr4:151882059-151882253	HepG2	liver:	n/a	n/a
50	CTCF	chr4:151882075-151882077	LNCaP	prostate:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:151875122-151875172	BE2_C	brain:	n/a
2	chr4:151875122-151875172	PANC-1	pancreas:	n/a
3	chr4:151875122-151875172	HIPEpiC	eye:	n/a
4	chr4:151875122-151875172	Hela-S3	cervix:	n/a
5	chr4:151875122-151875172	NH-A	brain:	n/a
6	chr4:151875122-151875172	RPTEC	kidney:	n/a
7	chr4:151875122-151875172	AG09309	skin:	n/a
8	chr4:151875122-151875172	ECC-1	luminal epithelium:	n/a
9	chr4:151875122-151875172	AG04450	lung:	fetal
10	chr4:151875122-151875172	HMEC	breast:	n/a
11	chr4:151875122-151875172	PFSK-1	brain:	n/a
12	chr4:151875122-151875172	HEEpiC	esophagus:	n/a
13	chr4:151875122-151875172	Caco-2	colon:	n/a
14	chr4:151875122-151875172	HUVEC	blood vessel:	n/a
15	chr4:151875122-151875172	T-47D	breast:	n/a
16	chr4:151875122-151875172	GM06990	blood:	n/a
17	chr4:151875122-151875172	HL-60	blood:	n/a
18	chr4:151875122-151875172	HCT-116	colon:	n/a
19	chr4:151875122-151875172	HRPEpiC	eye:	n/a
20	chr4:151875122-151875172	ProgFib	skin:	n/a
21	chr4:151875122-151875172	NT2-D1	testis:	n/a
22	chr4:151875122-151875172	SKMC	muscle:	n/a
23	chr4:151875122-151875172	HCM	heart:	n/a
24	chr4:151875122-151875172	GM12891	blood:	n/a
25	chr4:151875122-151875172	ovcar-3	ovarian:	n/a
26	chr4:151875122-151875172	SK-N-MC	brain:	n/a
27	chr4:151875122-151875172	AG04449	skin:	fetal
28	chr4:151875122-151875172	AoSMC	blood vessel:	n/a
29	chr4:151875122-151875172	HEK293	kidney:	embryo
30	chr4:151875122-151875172	MCF-7	breast:	n/a
31	chr4:151875122-151875172	AG09319	gingival:	n/a
32	chr4:151875122-151875172	H1-hESC	embryonic stem cell:	embryo
33	chr4:151875122-151875172	A549	lung:	n/a
34	chr4:151875122-151875172	SK-N-SH	brain:	n/a
35	chr4:151875122-151875172	GM19239	blood:	n/a
36	chr4:151875122-151875172	AG10803	skin:	n/a
37	chr4:151875122-151875172	CMK	blood:	n/a
38	chr4:151875122-151875172	GM12892	blood:	n/a
39	chr4:151875122-151875172	SK-N-SH_RA	brain:	n/a
40	chr4:151875122-151875172	HAEpiC	amniotic membrane:	n/a
41	chr4:151875122-151875172	IMR90	lung:	fetal
42	chr4:151875122-151875172	NHBE	bronchial:	n/a
43	chr4:151875122-151875172	PrEC	prostate:	n/a
44	chr4:151875122-151875172	HCPEpiC	choroid plexus:	n/a
45	chr4:151875122-151875172	Jurkat	blood:	n/a
46	chr4:151875122-151875172	BJ	skin:	n/a
47	chr4:151875122-151875172	HRCEpiC	kidney:	n/a
48	chr4:151875122-151875172	HPAEpiC	pulmonary alveolar:	n/a
49	chr4:151875122-151875172	HepG2	liver:	n/a
50	chr4:151875122-151875172	MCF10A-Er-Src	breast:	n/a

(count:22 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:151881135..151883794-chr4:151886997..151888968,2	MCF-7	breast:
2	chr4:151865757..151867781-chr4:151869547..151872879,3	K562	blood:
3	chr4:151872979..151875947-chr4:151936623..151938393,3	MCF-7	breast:
4	chr4:151877350..151879470-chr4:151882177..151883692,2	K562	blood:
5	chr4:151856044..151857786-chr4:151866410..151868032,2	MCF-7	breast:
6	chr4:151896819..151899555-chr4:151937310..151939113,2	K562	blood:
7	chr4:151881135..151883794-chr4:151886997..151888968,2	MCF-7	breast:
8	chr4:151881996..151883643-chr4:151936470..151938067,2	MCF-7	breast:
9	chr1:174358031..174358668-chr4:151874262..151874762,2	MCF-7	breast:
10	chr4:151858340..151860343-chr4:151871989..151873498,2	K562	blood:
11	chr4:151855396..151857375-chr4:151872035..151874195,2	K562	blood:
12	chr4:151866579..151869157-chr4:152019961..152022233,2	K562	blood:
13	chr4:151899256..151901793-chr4:151906070..151908890,2	K562	blood:
14	chr4:151899256..151901793-chr4:151906070..151908890,2	K562	blood:
15	chr4:151898127..151900327-chr4:151908207..151910681,2	K562	blood:
16	chr4:151865757..151867781-chr4:151869547..151872879,3	K562	blood:
17	chr4:151886113..151887964-chr4:151890160..151891760,2	K562	blood:
18	chr4:151877350..151879470-chr4:151882177..151883692,2	K562	blood:
19	chr4:151870335..151873445-chr4:152019879..152022004,3	K562	blood:
20	chr4:151890768..151892964-chr4:151894069..151896247,3	K562	blood:
21	chr4:151895289..151897770-chr4:151914690..151916756,2	MCF-7	breast:
22	chr4:151886113..151887964-chr4:151890160..151891760,2	K562	blood:

No data

Variant related genes	Relation type
RNA5SP168	TF binding region
RNA5SP168	CpG island
ENSG00000198589	chromatin interactions
ENSG00000252451	chromatin interactions
ENSG00000145425	chromatin interactions

Extended variants
information (count: 1400 )
Associated
traits (count: 77 )

Variant overlapped rSNPs/rCNVs (count:1400 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs573343775	chr4:151867069-151867070	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs549222495	chr4:151867112-151867113	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs182746883	chr4:151867141-151867142	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs540621960	chr4:151867143-151867144	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs577487990	chr4:151867152-151867153	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs540053155	chr4:151867162-151867163	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs111671302	chr4:151867225-151867226	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs553534112	chr4:151867241-151867242	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs573427482	chr4:151867248-151867249	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs185163731	chr4:151867249-151867250	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs145114440	chr4:151867250-151867251	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs115783353	chr4:151867293-151867294	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs368892056	chr4:151867304-151867305	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs552505667	chr4:151867317-151867318	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs189874786	chr4:151867357-151867358	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs547251041	chr4:151867425-151867426	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs540485364	chr4:151867466-151867467	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs553933235	chr4:151867475-151867476	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs77636934	chr4:151867480-151867481	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs529415366	chr4:151867557-151867558	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs1201209	chr4:151867584-151867585	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs569214109	chr4:151867639-151867640	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs538260021	chr4:151867658-151867659	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs78536083	chr4:151867741-151867742	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs375152064	chr4:151867742-151867743	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs398072328	chr4:151867747-151867748	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs143565036	chr4:151867754-151867755	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs114911443	chr4:151867758-151867759	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs563757481	chr4:151867795-151867796	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs183647094	chr4:151867796-151867797	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs531117646	chr4:151867800-151867801	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs553595332	chr4:151867865-151867866	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs115276873	chr4:151867868-151867869	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs72719702	chr4:151867870-151867871	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs368552275	chr4:151867884-151867885	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs556224477	chr4:151867921-151867922	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs34851464	chr4:151867928-151867929	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs544395714	chr4:151867937-151867938	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs562977533	chr4:151867943-151867944	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs77900092	chr4:151867974-151867975	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs576030777	chr4:151868015-151868016	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs545007942	chr4:151868025-151868026	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs561362555	chr4:151868033-151868034	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs34474606	chr4:151868069-151868070	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs78022254	chr4:151868070-151868071	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs564860867	chr4:151868107-151868108	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs1148639	chr4:151868298-151868299	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs567609954	chr4:151868340-151868341	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs543016036	chr4:151868379-151868380	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs560708859	chr4:151868440-151868441	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:77)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Medulloblastoma	21979893	CNVD
Neuroblastoma	18923191	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Colorectal cancer	19359472	CNVD
Malignant mesothelioma	18160781	CNVD
Medulloblastoma	18056178	CNVD
Multiple myeloma	17077331	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Oral squamous cell carcinoma	17134496	CNVD
4q-syndrome	17576883	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Muscular dystrophy	21149563	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Cervical cancer	21062161	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Lung cancer	18438408	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	21183584	CNVD
primary effusion lymphomas	17116491	CNVD
Breast cancer	16272173	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17133270	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital anomalies of the kidney and urinary tract	20505237	CNVD
Breast cancer	17393978	CNVD
Esophageal cancer	21851588	CNVD
Testicular germ cell tumor	18059402	CNVD
Ovarian cancer	22174824	CNVD
Olfactory neuroblastoma	18408657	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Ewing''s sarcoma	17952124	CNVD
Breast cancer	21633010	CNVD
Breast cancer	21364760	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Non-small cell lung cancer	21829676	CNVD
Breast cancer	17588203	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Breast cancer	22522925	CNVD
Cancer	20164919	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Schizophrenia	20967226	CNVD

Chromatin state (count:597 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:151796200-151872000	Weak transcription	Psoas Muscle	Psoas
2	chr4:151796400-151886600	Weak transcription	Pancreas	Pancrea
3	chr4:151846400-151873800	Weak transcription	Fetal Intestine Small	intestine
4	chr4:151849400-151878000	Weak transcription	Primary B cells from cord blood	blood
5	chr4:151850200-151867400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
6	chr4:151850200-151873800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
7	chr4:151858600-151870400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
8	chr4:151859800-151882200	Weak transcription	Aorta	Aorta
9	chr4:151860600-151868000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
10	chr4:151860800-151879000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
11	chr4:151861000-151878600	Weak transcription	Primary T helper cells fromperipheralblood	blood
12	chr4:151861200-151867800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
13	chr4:151861200-151870600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
14	chr4:151861400-151867400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
15	chr4:151861600-151872200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
16	chr4:151861800-151871800	Weak transcription	Primary T cells from cord blood	blood
17	chr4:151864800-151869600	Enhancers	Primary T helper cells PMA-I stimulated	--
18	chr4:151865000-151867400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
19	chr4:151865000-151869600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
20	chr4:151865200-151882000	Weak transcription	Ovary	ovary
21	chr4:151865200-151883400	Weak transcription	Gastric	stomach
22	chr4:151865400-151867400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
23	chr4:151865400-151879000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
24	chr4:151866800-151871200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
25	chr4:151866800-151871800	Weak transcription	Primary B cells from peripheral blood	blood
26	chr4:151866800-151871800	Weak transcription	K562	blood
27	chr4:151867000-151867400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
28	chr4:151867400-151867600	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
29	chr4:151867400-151868200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chr4:151867400-151868400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
31	chr4:151867400-151868400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
32	chr4:151867400-151868800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
33	chr4:151867400-151869600	Enhancers	Primary hematopoietic stem cells short term culture	blood
34	chr4:151867600-151873600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
35	chr4:151867800-151868200	Enhancers	Liver	Liver
36	chr4:151867800-151869000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
37	chr4:151868200-151868600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
38	chr4:151868200-151868600	Weak transcription	Liver	Liver
39	chr4:151868400-151868800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
40	chr4:151868400-151868800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
41	chr4:151868600-151868800	Enhancers	Liver	Liver
42	chr4:151868600-151869600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
43	chr4:151868800-151869000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
44	chr4:151868800-151869000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
45	chr4:151868800-151869000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
46	chr4:151868800-151871800	Weak transcription	Liver	Liver
47	chr4:151869000-151870400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
48	chr4:151869000-151871600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
49	chr4:151869000-151873200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
50	chr4:151869000-151873200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--

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