Variant report

Variant	nsv880247
Chromosome Location	chr4:150057979-150159936
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:341)
CpG islands
(count:183)
Chromatin interactive
region (count:5)
LncRNA
region (count:14)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:341 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BCL11A	chr4:150085578-150085819	H1-hESC	embryonic stem cell:	n/a	n/a
2	CEBPB	chr4:150155028-150155228	IMR90	lung:	n/a	n/a
3	CEBPB	chr4:150089802-150090171	IMR90	lung:	n/a	chr4:150089983-150089994 chr4:150089982-150089993 chr4:150089982-150089995
4	CEBPB	chr4:150089964-150090273	H1-hESC	embryonic stem cell:	n/a	chr4:150089983-150089994 chr4:150089982-150089993 chr4:150089982-150089995
5	CEBPB	chr4:150130695-150130739	H1-hESC	embryonic stem cell:	n/a	n/a
6	CEBPB	chr4:150089819-150090159	HepG2	liver:	n/a	chr4:150089983-150089994 chr4:150089982-150089993 chr4:150089982-150089995
7	CEBPB	chr4:150109374-150109673	HepG2	liver:	n/a	chr4:150109488-150109499
8	CEBPB	chr4:150103753-150104034	HepG2	liver:	n/a	chr4:150103910-150103923 chr4:150103911-150103922 chr4:150103912-150103921
9	CEBPB	chr4:150130637-150130875	HepG2	liver:	n/a	n/a
10	CEBPB	chr4:150081486-150081932	ECC-1	luminal epithelium:	n/a	n/a
11	CHD2	chr4:150126306-150126345	HepG2	liver:	n/a	n/a
12	CTCF	chr4:150085560-150085710	AG09319	gingival:	n/a	n/a
13	CTCF	chr4:150112388-150112440	Fibrobl	skin:	n/a	chr4:150112392-150112405 chr4:150112391-150112407 chr4:150112397-150112405 chr4:150112390-150112408
14	CTCF	chr4:150093720-150093870	AG04450	lung:	n/a	n/a
15	CTCF	chr4:150085620-150085770	BJ	skin:	n/a	n/a
16	CTCF	chr4:150085580-150085730	HRPEpiC	eye:	n/a	n/a
17	CTCF	chr4:150112300-150112450	AG10803	skin:	n/a	chr4:150112392-150112405 chr4:150112385-150112406 chr4:150112391-150112407 chr4:150112397-150112405 chr4:150112390-150112408
18	CTCF	chr4:150085620-150085770	AG04450	lung:	n/a	n/a
19	CTCF	chr4:150107916-150107950	K562	blood:	n/a	n/a
20	CTCF	chr4:150112385-150112408	MCF-7	breast:	n/a	chr4:150112392-150112405 chr4:150112385-150112406 chr4:150112391-150112407 chr4:150112397-150112405 chr4:150112390-150112408
21	CTCF	chr4:150085540-150085690	HCPEpiC	choroid plexus:	n/a	n/a
22	CTCF	chr4:150085560-150085710	HA-sp	spinal cord:	n/a	n/a
23	CTCF	chr4:150074900-150075050	MCF-7	breast:	n/a	n/a
24	CTCF	chr4:150085580-150085730	AG10803	skin:	n/a	n/a
25	CTCF	chr4:150085560-150085710	HPF	lung:	n/a	n/a
26	CTCF	chr4:150069460-150069610	AG10803	skin:	n/a	n/a
27	CTCF	chr4:150075020-150075170	WERI-Rb-1	eye:	n/a	n/a
28	CTCF	chr4:150075116-150075162	Hela-S3	cervix:	n/a	n/a
29	CTCF	chr4:150085620-150085770	HCPEpiC	choroid plexus:	n/a	n/a
30	CTCF	chr4:150112140-150112290	AG09319	gingival:	n/a	n/a
31	CTCF	chr4:150074989-150075254	MCF-7	breast:	n/a	n/a
32	CTCF	chr4:150085640-150085790	AG10803	skin:	n/a	n/a
33	CTCF	chr4:150112340-150112490	AG09319	gingival:	n/a	chr4:150112392-150112405 chr4:150112385-150112406 chr4:150112391-150112407 chr4:150112397-150112405 chr4:150112390-150112408
34	CTCF	chr4:150085640-150085790	BJ	skin:	n/a	n/a
35	CTCF	chr4:150085605-150085770	ProgFib	skin:	n/a	n/a
36	CTCF	chr4:150112376-150112437	LNCaP	prostate:	n/a	chr4:150112392-150112405 chr4:150112385-150112406 chr4:150112391-150112407 chr4:150112397-150112405 chr4:150112390-150112408
37	CTCF	chr4:150150785-150150835	LNCaP	prostate:	n/a	n/a
38	CTCF	chr4:150143662-150143674	GM10248	blood:	n/a	n/a
39	CTCF	chr4:150085540-150085690	HMF	breast:	n/a	n/a
40	CTCF	chr4:150085600-150085750	AG04449	skin:	n/a	n/a
41	CTCF	chr4:150085480-150085630	AG09309	skin:	n/a	n/a
42	CTCF	chr4:150075100-150075250	MCF-7	breast:	n/a	n/a
43	CTCF	chr4:150085560-150085710	HPAF	blood vessel:	n/a	n/a
44	CTCF	chr4:150135014-150135039	Spleen_OC	spleen:	n/a	n/a
45	CTCF	chr4:150085599-150085803	Fibrobl	skin:	n/a	n/a
46	CTCF	chr4:150085580-150085730	HBMEC	blood vessel:	n/a	n/a
47	CTCF	chr4:150101652-150101695	LNCaP	prostate:	n/a	n/a
48	CTCF	chr4:150085540-150085690	HPAF	blood vessel:	n/a	n/a
49	CTCF	chr4:150085520-150085670	AG09309	skin:	n/a	n/a
50	CTCF	chr4:150085592-150085787	Gliobla	brain:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:150085703-150085753	NB4	blood:	n/a
2	chr4:150087191-150087241	HEK293	kidney:	embryo
3	chr4:150067050-150067100	BE2_C	brain:	n/a
4	chr4:150067050-150067100	HCF	heart:	n/a
5	chr4:150087191-150087241	HIPEpiC	eye:	n/a
6	chr4:150067050-150067100	NH-A	brain:	n/a
7	chr4:150067050-150067100	H1-hESC	embryonic stem cell:	embryo
8	chr4:150087191-150087241	AG04449	skin:	fetal
9	chr4:150085703-150085753	HepG2	liver:	n/a
10	chr4:150085703-150085753	ovcar-3	ovarian:	n/a
11	chr4:150067050-150067100	GM12891	blood:	n/a
12	chr4:150085703-150085753	MCF10A-Er-Src	breast:	n/a
13	chr4:150087191-150087241	NHBE	bronchial:	n/a
14	chr4:150085703-150085753	LNCaP	prostate:	n/a
15	chr4:150085703-150085753	IMR90	lung:	fetal
16	chr4:150087191-150087241	H1-hESC	embryonic stem cell:	embryo
17	chr4:150087191-150087241	Caco-2	colon:	n/a
18	chr4:150067050-150067100	RPTEC	kidney:	n/a
19	chr4:150087191-150087241	AoSMC	blood vessel:	n/a
20	chr4:150067050-150067100	IMR90	lung:	fetal
21	chr4:150087191-150087241	GM12891	blood:	n/a
22	chr4:150085703-150085753	HRPEpiC	eye:	n/a
23	chr4:150085703-150085753	T-47D	breast:	n/a
24	chr4:150087191-150087241	HPAEpiC	pulmonary alveolar:	n/a
25	chr4:150067050-150067100	LNCaP	prostate:	n/a
26	chr4:150067050-150067100	NHBE	bronchial:	n/a
27	chr4:150067050-150067100	HMEC	breast:	n/a
28	chr4:150085703-150085753	AG04450	lung:	fetal
29	chr4:150085703-150085753	NH-A	brain:	n/a
30	chr4:150085703-150085753	HRE	kidney:	n/a
31	chr4:150067050-150067100	ProgFib	skin:	n/a
32	chr4:150067050-150067100	HPAEpiC	pulmonary alveolar:	n/a
33	chr4:150067050-150067100	Caco-2	colon:	n/a
34	chr4:150067050-150067100	HIPEpiC	eye:	n/a
35	chr4:150087191-150087241	AG09319	gingival:	n/a
36	chr4:150085703-150085753	GM19239	blood:	n/a
37	chr4:150087191-150087241	HCT-116	colon:	n/a
38	chr4:150085703-150085753	HCPEpiC	choroid plexus:	n/a
39	chr4:150085703-150085753	NHDF-neo	bronchial:	n/a
40	chr4:150067050-150067100	Jurkat	blood:	n/a
41	chr4:150087191-150087241	HEEpiC	esophagus:	n/a
42	chr4:150085703-150085753	PrEC	prostate:	n/a
43	chr4:150087191-150087241	MCF-7	breast:	n/a
44	chr4:150087191-150087241	SKMC	muscle:	n/a
45	chr4:150087191-150087241	HRPEpiC	eye:	n/a
46	chr4:150087191-150087241	IMR90	lung:	fetal
47	chr4:150085703-150085753	HCM	heart:	n/a
48	chr4:150067050-150067100	AoSMC	blood vessel:	n/a
49	chr4:150087191-150087241	HCM	heart:	n/a
50	chr4:150085703-150085753	AG10803	skin:	n/a

(count:5 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:150063409..150066191-chr4:150071536..150073450,2	K562	blood:
2	chr4:150107886..150110536-chr4:150111462..150113624,2	K562	blood:
3	chr4:150063409..150066191-chr4:150071536..150073450,2	K562	blood:
4	chr4:150107886..150110536-chr4:150111462..150113624,2	K562	blood:
5	chr4:150074768..150075429-chr4:150185153..150186021,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NR3C2-4	chr4:150070701-150070932	XLOC_004120
2	lnc-DCLK2-3	chr4:150125045-150125304	NONHSAT098714
3	lnc-NR3C2-4	chr4:150068954-150069197	XLOC_004120
4	lnc-NR3C2-4	chr4:150071377-150071438	XLOC_004120
5	lnc-NR3C2-4	chr4:150068965-150069197	XLOC_004120
6	lnc-DCLK2-3	chr4:150139117-150139172	NONHSAT098714
7	lnc-DCLK2-3	chr4:150076604-150076877	NONHSAT098714
8	lnc-DCLK2-3	chr4:150123515-150123708	NONHSAT098714
9	lnc-NR3C2-4	chr4:150070701-150070929	XLOC_004120
10	lnc-DCLK2-3	chr4:150135596-150135683	NONHSAT098714
11	lnc-DCLK2-3	chr4:150126059-150126366	NONHSAT098714
12	lnc-DCLK2-3	chr4:150135803-150136039	NONHSAT098714
13	lnc-DCLK2-3	chr4:150075447-150075771	NONHSAT098714
14	lnc-DCLK2-3	chr4:150137555-150137729	NONHSAT098714

No data

Variant related genes	Relation type
ENSG00000248210	TF binding region
ENSG00000250252	TF binding region
ENSG00000248210	CpG island
ENSG00000250252	CpG island

Extended variants
information (count: 1682 )
Associated
traits (count: 73 )

Variant overlapped rSNPs/rCNVs (count:1682 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1438766	chr4:150057979-150057980	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs560120732	chr4:150058064-150058065	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs577209177	chr4:150058078-150058079	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs183820377	chr4:150058146-150058147	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs555727592	chr4:150058184-150058185	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs575962009	chr4:150058195-150058196	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs187881706	chr4:150058207-150058208	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs9998116	chr4:150058315-150058316	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs558757623	chr4:150058316-150058317	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs572156678	chr4:150058330-150058331	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs541174667	chr4:150058346-150058347	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs183333423	chr4:150058411-150058412	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs74388463	chr4:150058454-150058455	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs139066883	chr4:150058474-150058475	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs79523622	chr4:150058508-150058509	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs111944626	chr4:150058516-150058517	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs146873562	chr4:150058551-150058552	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs571868046	chr4:150058557-150058558	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs7441940	chr4:150058559-150058560	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs564181472	chr4:150058575-150058576	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs187072116	chr4:150058582-150058583	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs374473779	chr4:150058642-150058643	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs140679683	chr4:150058645-150058646	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs191711508	chr4:150058667-150058668	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs555790901	chr4:150058692-150058693	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs183163300	chr4:150058697-150058698	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs78144373	chr4:150058709-150058710	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs538207954	chr4:150058725-150058726	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs558580070	chr4:150058840-150058841	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs568716422	chr4:150058936-150058937	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs187494687	chr4:150058951-150058952	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs4627842	chr4:150058978-150058979	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs540882679	chr4:150058980-150058981	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs554732526	chr4:150058997-150058998	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs79610734	chr4:150059020-150059021	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs543141130	chr4:150059045-150059046	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs111512485	chr4:150059079-150059080	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs576512102	chr4:150059097-150059098	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs116579205	chr4:150059102-150059103	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs565459014	chr4:150059123-150059124	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs193297980	chr4:150059127-150059128	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs367746859	chr4:150059129-150059130	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs547706365	chr4:150059148-150059149	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs185370808	chr4:150059155-150059156	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs17025719	chr4:150059182-150059183	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs189483104	chr4:150059190-150059191	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs116473964	chr4:150059199-150059200	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs370153710	chr4:150059379-150059380	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs143762678	chr4:150059386-150059387	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs565868162	chr4:150059401-150059402	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:73)

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
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	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
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Breast cancer	21364760	CNVD
Epilepsy	22083797	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Acute lymphoblastic leukemia	21248843	CNVD

Chromatin state (count:232 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:150057400-150058400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
2	chr4:150058000-150058800	Enhancers	Fetal Muscle Leg	muscle
3	chr4:150058200-150058600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
4	chr4:150058400-150058600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
5	chr4:150058400-150059800	Enhancers	Fetal Stomach	stomach
6	chr4:150058600-150066600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
7	chr4:150058800-150059200	Enhancers	NHDF-Ad	bronchial
8	chr4:150058800-150059800	Weak transcription	Fetal Muscle Leg	muscle
9	chr4:150059200-150062400	Weak transcription	NHDF-Ad	bronchial
10	chr4:150060000-150060200	Active TSS	Muscle Satellite Cultured Cells	--
11	chr4:150060000-150060200	Enhancers	Fetal Muscle Leg	muscle
12	chr4:150060200-150060400	Flanking Active TSS	Muscle Satellite Cultured Cells	--
13	chr4:150060400-150063200	Enhancers	Muscle Satellite Cultured Cells	--
14	chr4:150061000-150061600	Enhancers	iPS-18 Cell Line	embryonic stem cell
15	chr4:150061000-150062600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr4:150061200-150061600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr4:150061200-150061600	Enhancers	HUES6 Cell Line	embryonic stem cell
18	chr4:150061400-150062600	Enhancers	HSMM	muscle
19	chr4:150061800-150062800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
20	chr4:150062400-150063200	Enhancers	NHDF-Ad	bronchial
21	chr4:150062600-150063400	Enhancers	Fetal Lung	lung
22	chr4:150062600-150066800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
23	chr4:150062600-150066800	Weak transcription	HSMM	muscle
24	chr4:150063200-150066200	Weak transcription	NHDF-Ad	bronchial
25	chr4:150063200-150066800	Weak transcription	Muscle Satellite Cultured Cells	--
26	chr4:150066200-150068200	Enhancers	NHDF-Ad	bronchial
27	chr4:150066600-150068400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
28	chr4:150066800-150067200	Enhancers	HSMM	muscle
29	chr4:150066800-150067200	Enhancers	Osteobl	bone
30	chr4:150066800-150067400	Enhancers	Muscle Satellite Cultured Cells	--
31	chr4:150066800-150067400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
32	chr4:150066800-150067400	Enhancers	NH-A	brain
33	chr4:150066800-150067400	Enhancers	NHLF	lung
34	chr4:150068400-150068800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
35	chr4:150068800-150069400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
36	chr4:150069000-150069600	Enhancers	Fetal Kidney	kidney
37	chr4:150078600-150080800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chr4:150079400-150080200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
39	chr4:150079400-150081000	Enhancers	NHLF	lung
40	chr4:150079400-150083000	Enhancers	NHDF-Ad	bronchial
41	chr4:150079800-150080600	Enhancers	Muscle Satellite Cultured Cells	--
42	chr4:150080200-150080400	Enhancers	HSMM	muscle
43	chr4:150080200-150080600	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
44	chr4:150080400-150080600	Enhancers	Osteobl	bone
45	chr4:150080400-150081800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
46	chr4:150080400-150081800	Weak transcription	HSMM	muscle
47	chr4:150080600-150081600	Weak transcription	Osteobl	bone
48	chr4:150080600-150082000	Weak transcription	Muscle Satellite Cultured Cells	--
49	chr4:150080600-150085200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
50	chr4:150080800-150082200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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