Variant report

Variant	nsv880387
Chromosome Location	chr4:187845057-187943614
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:812)
CpG islands
(count:1468)
Chromatin interactive
region (count:23)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:812 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:187853628-187853802	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:187868629-187868925	HepG2	liver:	n/a	n/a
3	ARID3A	chr4:187857788-187858659	HepG2	liver:	n/a	n/a
4	ARID3A	chr4:187867829-187868202	HepG2	liver:	n/a	n/a
5	ARID3A	chr4:187861751-187861928	HepG2	liver:	n/a	n/a
6	ATF1	chr4:187861013-187861279	K562	blood:	n/a	n/a
7	BACH1	chr4:187938365-187938620	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr4:187870229-187870474	H1-hESC	embryonic stem cell:	n/a	n/a
9	BHLHE40	chr4:187867852-187868124	HepG2	liver:	n/a	n/a
10	CBX3	chr4:187853176-187854694	HCT-116	colon:	n/a	n/a
11	CBX3	chr4:187857745-187858737	HCT-116	colon:	n/a	n/a
12	CBX3	chr4:187853152-187854568	HCT-116	colon:	n/a	n/a
13	CBX3	chr4:187850180-187850774	HCT-116	colon:	n/a	n/a
14	CBX3	chr4:187848532-187849172	HCT-116	colon:	n/a	n/a
15	CEBPB	chr4:187863864-187864222	Hela-S3	cervix:	n/a	chr4:187864080-187864091
16	CEBPB	chr4:187864692-187864880	IMR90	lung:	n/a	chr4:187864774-187864785
17	CEBPB	chr4:187856022-187856518	MCF-7	breast:	n/a	chr4:187856291-187856302
18	CEBPB	chr4:187863884-187864367	IMR90	lung:	n/a	chr4:187864080-187864091
19	CEBPB	chr4:187852728-187854633	HCT-116	colon:	n/a	chr4:187852912-187852923 chr4:187853362-187853379 chr4:187852911-187852922
20	CEBPB	chr4:187852609-187855078	HCT-116	colon:	n/a	chr4:187854661-187854674 chr4:187852912-187852923 chr4:187853362-187853379 chr4:187852911-187852922 chr4:187854661-187854672 chr4:187854661-187854674
21	CEBPB	chr4:187852790-187853007	K562	blood:	n/a	chr4:187852912-187852923 chr4:187852911-187852922
22	CEBPB	chr4:187923422-187923659	HepG2	liver:	n/a	chr4:187923465-187923476
23	CEBPB	chr4:187923364-187923655	A549	lung:	n/a	chr4:187923465-187923476
24	CEBPB	chr4:187852720-187853101	IMR90	lung:	n/a	chr4:187852912-187852923 chr4:187852911-187852922
25	CEBPB	chr4:187923457-187923475	K562	blood:	n/a	n/a
26	CEBPB	chr4:187861713-187861987	HepG2	liver:	n/a	n/a
27	CEBPB	chr4:187864023-187864107	K562	blood:	n/a	chr4:187864080-187864091
28	CEBPB	chr4:187852834-187853004	HepG2	liver:	n/a	chr4:187852912-187852923 chr4:187852911-187852922
29	CEBPB	chr4:187869806-187870313	IMR90	lung:	n/a	chr4:187869972-187869984
30	CEBPB	chr4:187850155-187850790	HCT-116	colon:	n/a	n/a
31	CEBPB	chr4:187856204-187856429	HepG2	liver:	n/a	chr4:187856291-187856302
32	CEBPB	chr4:187863984-187864144	HepG2	liver:	n/a	chr4:187864080-187864091
33	CEBPB	chr4:187857692-187858706	HCT-116	colon:	n/a	n/a
34	CEBPB	chr4:187863846-187864263	HepG2	liver:	n/a	chr4:187864080-187864091
35	CEBPB	chr4:187858200-187858563	HepG2	liver:	n/a	n/a
36	CEBPB	chr4:187863784-187864213	A549	lung:	n/a	chr4:187864080-187864091
37	CEBPB	chr4:187862226-187862465	HepG2	liver:	n/a	n/a
38	CEBPB	chr4:187858205-187858555	A549	lung:	n/a	n/a
39	CEBPB	chr4:187923410-187923599	H1-hESC	embryonic stem cell:	n/a	chr4:187923465-187923476
40	CEBPB	chr4:187927557-187927886	IMR90	lung:	n/a	chr4:187927733-187927746
41	CEBPB	chr4:187901045-187901530	IMR90	lung:	n/a	chr4:187901511-187901522 chr4:187901356-187901373
42	CEBPB	chr4:187930239-187930492	HepG2	liver:	n/a	chr4:187930359-187930370
43	CEBPB	chr4:187923294-187923654	IMR90	lung:	n/a	chr4:187923465-187923476
44	CEBPB	chr4:187856143-187856450	IMR90	lung:	n/a	chr4:187856291-187856302
45	CHD2	chr4:187867964-187868134	Hela-S3	cervix:	n/a	n/a
46	CTCF	chr4:187870220-187870370	SK-N-SH_RA	brain:	n/a	n/a
47	CTCF	chr4:187858340-187858490	HPAF	blood vessel:	n/a	n/a
48	CTCF	chr4:187870187-187870412	Medullo	brain:	n/a	n/a
49	CTCF	chr4:187848985-187849005	MCF-7	breast:	n/a	chr4:187848994-187849002 chr4:187848995-187849003 chr4:187848989-187849002
50	CTCF	chr4:187867900-187868050	AG04449	skin:	n/a	chr4:187867983-187867991

(count:1468 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:187851586-187851636	Jurkat	blood:	n/a
2	chr4:187882934-187882984	HMEC	breast:	n/a
3	chr4:187891568-187891618	PFSK-1	brain:	n/a
4	chr4:187882934-187882984	HL-60	blood:	n/a
5	chr4:187851586-187851636	Jurkat	blood:	n/a
6	chr4:187882934-187882984	HMEC	breast:	n/a
7	chr4:187891568-187891618	PFSK-1	brain:	n/a
8	chr4:187882934-187882984	HL-60	blood:	n/a
9	chr4:187864009-187864059	Jurkat	blood:	n/a
10	chr4:187869873-187869923	A549	lung:	n/a
11	chr4:187851586-187851636	GM12878	blood:	n/a
12	chr4:187889614-187889664	NHBE	bronchial:	n/a
13	chr4:187864009-187864059	Caco-2	colon:	n/a
14	chr4:187893119-187893169	Hela-S3	cervix:	n/a
15	chr4:187851405-187851455	T-47D	breast:	n/a
16	chr4:187887005-187887055	MCF10A-Er-Src	breast:	n/a
17	chr4:187851586-187851636	IMR90	lung:	fetal
18	chr4:187851405-187851455	AG04450	lung:	fetal
19	chr4:187851586-187851636	BJ	skin:	n/a
20	chr4:187882934-187882984	HIPEpiC	eye:	n/a
21	chr4:187891568-187891618	HRE	kidney:	n/a
22	chr4:187927166-187927216	SK-N-SH_RA	brain:	n/a
23	chr4:187887005-187887055	Hela-S3	cervix:	n/a
24	chr4:187869873-187869923	T-47D	breast:	n/a
25	chr4:187893119-187893169	ProgFib	skin:	n/a
26	chr4:187885870-187885920	T-47D	breast:	n/a
27	chr4:187894584-187894634	GM06990	blood:	n/a
28	chr4:187851418-187851468	AoSMC	blood vessel:	n/a
29	chr4:187885870-187885920	HUVEC	blood vessel:	n/a
30	chr4:187887742-187887792	HUVEC	blood vessel:	n/a
31	chr4:187891568-187891618	NH-A	brain:	n/a
32	chr4:187855570-187855620	H1-hESC	embryonic stem cell:	embryo
33	chr4:187851333-187851383	HCPEpiC	choroid plexus:	n/a
34	chr4:187894704-187894754	AG09319	gingival:	n/a
35	chr4:187869873-187869923	HAEpiC	amniotic membrane:	n/a
36	chr4:187894704-187894754	AG10803	skin:	n/a
37	chr4:187927166-187927216	AG09309	skin:	n/a
38	chr4:187885870-187885920	AoSMC	blood vessel:	n/a
39	chr4:187880263-187880313	GM12878	blood:	n/a
40	chr4:187851405-187851455	NHDF-neo	bronchial:	n/a
41	chr4:187855570-187855620	ProgFib	skin:	n/a
42	chr4:187851333-187851383	NHBE	bronchial:	n/a
43	chr4:187892539-187892589	HRPEpiC	eye:	n/a
44	chr4:187855570-187855620	GM12892	blood:	n/a
45	chr4:187887742-187887792	A549	lung:	n/a
46	chr4:187855570-187855620	NT2-D1	testis:	n/a
47	chr4:187881888-187881938	CMK	blood:	n/a
48	chr4:187891568-187891618	HCT-116	colon:	n/a
49	chr4:187881888-187881938	ProgFib	skin:	n/a
50	chr4:187889614-187889664	HCPEpiC	choroid plexus:	n/a

(count:23 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:187658603..187659281-chr4:187867789..187868472,2	MCF-7	breast:
2	chr4:187844136..187846877-chr4:187850742..187852747,2	K562	blood:
3	chr4:187910556..187913594-chr4:187916872..187920065,3	K562	blood:
4	chr4:187867875..187869719-chr4:187871363..187873618,2	MCF-7	breast:
5	chr4:187848247..187850848-chr4:187854272..187856829,2	K562	blood:
6	chr4:187910556..187913594-chr4:187916872..187920065,3	K562	blood:
7	chr4:187867684..187870026-chr4:187872421..187875152,2	MCF-7	breast:
8	chr4:187848247..187850848-chr4:187854272..187856829,2	K562	blood:
9	chr4:187838828..187841268-chr4:187853169..187855944,2	K562	blood:
10	chr4:187647203..187650083-chr4:187858614..187861044,2	MCF-7	breast:
11	chr4:187648351..187650879-chr4:187855816..187858244,2	MCF-7	breast:
12	chr4:187645972..187647664-chr4:187867143..187868450,8	MCF-7	breast:
13	chr4:187676723..187679624-chr4:187847276..187848972,2	K562	blood:
14	chr4:187939165..187941494-chr4:187941726..187943652,2	K562	blood:
15	chr4:187844136..187846877-chr4:187850742..187852747,2	K562	blood:
16	chr4:187867684..187870026-chr4:187872421..187875152,2	MCF-7	breast:
17	chr4:187702948..187705032-chr4:187853740..187855963,2	K562	blood:
18	chr4:187648031..187648672-chr4:187867515..187868384,2	MCF-7	breast:
19	chr4:187644629..187648780-chr4:187865976..187870182,7	MCF-7	breast:
20	chr4:187759553..187761639-chr4:187893343..187896166,2	K562	blood:
21	chr4:187646857..187647583-chr4:187867241..187868105,3	MCF-7	breast:
22	chr4:187641888..187650885-chr4:187865376..187870322,9	MCF-7	breast:
23	chr4:187867875..187869719-chr4:187871363..187873618,2	MCF-7	breast:

(count:3 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAT1-1	chr4:187900644-187900886	XLOC_004215
2	lnc-FAT1-1	chr4:187943080-187943127	XLOC_004215
3	lnc-FAT1-1	chr4:187917410-187917592	XLOC_004215

No data

Variant related genes	Relation type
ENSG00000249742	TF binding region
ENSG00000249742	CpG island
ENSG00000083857	chromatin interactions
ENSG00000249742	chromatin interactions

Extended variants
information (count: 3420 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:3420 , 50 per page) page: 1 2 3 4 5 6 7 ... 69

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10033110	chr4:187845057-187845058	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs372758625	chr4:187845081-187845082	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs547859770	chr4:187845083-187845084	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs571104582	chr4:187845101-187845102	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs539991680	chr4:187845108-187845109	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs556912210	chr4:187845129-187845130	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs570336463	chr4:187845135-187845136	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs536126193	chr4:187845148-187845149	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs555104796	chr4:187845239-187845240	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs571999203	chr4:187845240-187845241	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs534468159	chr4:187845276-187845277	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs78436011	chr4:187845292-187845293	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs370364071	chr4:187845336-187845337	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs62343117	chr4:187845347-187845348	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs543176917	chr4:187845410-187845411	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs148634502	chr4:187845414-187845415	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs183165103	chr4:187845415-187845416	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs374332793	chr4:187845422-187845423	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs537723637	chr4:187845424-187845425	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs188442331	chr4:187845462-187845463	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs191998077	chr4:187845475-187845476	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs561980661	chr4:187845499-187845500	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs527681977	chr4:187845511-187845512	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs559320392	chr4:187845557-187845558	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs11721604	chr4:187845560-187845561	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs144084894	chr4:187845602-187845603	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs533589611	chr4:187845610-187845611	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs538604082	chr4:187845687-187845688	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs199527643	chr4:187845722-187845723	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs570249733	chr4:187845750-187845751	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs535815944	chr4:187845788-187845789	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs6815445	chr4:187845789-187845790	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs565546404	chr4:187845802-187845803	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs142946035	chr4:187845808-187845809	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs200115265	chr4:187845818-187845819	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs141105421	chr4:187845819-187845820	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs372201018	chr4:187845822-187845823	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs184929398	chr4:187845846-187845847	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs577287627	chr4:187845850-187845851	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs536725599	chr4:187845857-187845858	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs189638486	chr4:187845873-187845874	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs375515912	chr4:187845894-187845895	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs573490165	chr4:187845904-187845905	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs542601812	chr4:187845914-187845915	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs571999667	chr4:187845940-187845941	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs147719405	chr4:187845956-187845957	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs200539023	chr4:187845986-187845987	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs115409141	chr4:187845988-187845989	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs533687860	chr4:187845993-187845994	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs143956984	chr4:187846009-187846010	ZNF genes & repeats Enhancers Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:82)

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
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
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
Breast cancer	16608533	CNVD
Wilms tumour	21544195	CNVD
Lung cancer	18438408	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Breast cancer	16272173	CNVD
Breast cancer	17133270	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital anomalies of the kidney and urinary tract	20505237	CNVD
Testicular germ cell tumor	18059402	CNVD
Ovarian cancer	22174824	CNVD
Olfactory neuroblastoma	18408657	CNVD
Breast cancer	21785460	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Ewing''s sarcoma	17952124	CNVD
Breast cancer	21633010	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20581869	CNVD
Hepatocellular carcinoma	16750200	CNVD
abnormal development	18461090	CNVD
Neuroblastoma	16790693	CNVD
Colorectal cancer	16774939	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Basal cell lymphoma	17053054	CNVD
Facioscapulohumeral muscular dystrophy	21829175	CNVD
Disorders of sex development	21048976	CNVD
Ovarian cancer	20844748	CNVD
Autism	18414403	CNVD
Urothelial carcinoma	21177765	CNVD
Cancer	20164920	CNVD
Cancer	20164919	CNVD
Breast cancer	20409316	CNVD
Rhabdomyosarcoma	16790082	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	21399695	CNVD
Developmental delay	22127048	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Cervical cancer	21063398	CNVD
Oral cancer	21386901	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Oral cancer	17325662	CNVD

Chromatin state (count:768 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:187837200-187863800	Weak transcription	Right Atrium	heart
2	chr4:187840000-187853400	Weak transcription	Fetal Kidney	kidney
3	chr4:187840400-187846000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr4:187842000-187845400	Weak transcription	Fetal Lung	lung
5	chr4:187842000-187852400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
6	chr4:187842200-187845400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
7	chr4:187842200-187845600	Weak transcription	HSMM	muscle
8	chr4:187842400-187845400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr4:187842400-187845400	Weak transcription	Muscle Satellite Cultured Cells	--
10	chr4:187842400-187845400	Weak transcription	NHDF-Ad	bronchial
11	chr4:187842400-187845400	Weak transcription	NHLF	lung
12	chr4:187842400-187845400	Weak transcription	Osteobl	bone
13	chr4:187842400-187846000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr4:187842600-187845400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
15	chr4:187842600-187845400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr4:187842600-187845800	Weak transcription	HSMMtube	muscle
17	chr4:187842600-187846000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
18	chr4:187842600-187846000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
19	chr4:187842600-187848600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr4:187842600-187852200	Weak transcription	HMEC	breast
21	chr4:187842800-187845800	Weak transcription	NHEK	skin
22	chr4:187844800-187845400	Weak transcription	NH-A	brain
23	chr4:187845200-187846000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
24	chr4:187845400-187845600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
25	chr4:187845400-187845800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
26	chr4:187845400-187845800	Enhancers	NHDF-Ad	bronchial
27	chr4:187845400-187846000	Enhancers	Muscle Satellite Cultured Cells	--
28	chr4:187845400-187846200	Enhancers	NH-A	brain
29	chr4:187845400-187846200	Enhancers	Osteobl	bone
30	chr4:187845400-187846400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
31	chr4:187845400-187846400	Enhancers	Fetal Lung	lung
32	chr4:187845400-187846400	Enhancers	NHLF	lung
33	chr4:187845400-187846800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
34	chr4:187845600-187846000	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
35	chr4:187845600-187846400	Enhancers	HSMM	muscle
36	chr4:187845800-187846200	Enhancers	Fetal Heart	heart
37	chr4:187845800-187846200	Enhancers	NHEK	skin
38	chr4:187845800-187846400	Enhancers	HSMMtube	muscle
39	chr4:187845800-187846400	Flanking Active TSS	NHDF-Ad	bronchial
40	chr4:187845800-187851200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
41	chr4:187846000-187846200	Enhancers	Breast Myoepithelial Primary Cells	Breast
42	chr4:187846000-187846200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
43	chr4:187846000-187846200	Flanking Bivalent TSS/Enh	Fetal Brain Male	brain
44	chr4:187846000-187846400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
45	chr4:187846000-187846400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
46	chr4:187846000-187846400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr4:187846000-187846400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
48	chr4:187846000-187846400	Enhancers	Gastric	stomach
49	chr4:187846000-187850400	Weak transcription	Muscle Satellite Cultured Cells	--
50	chr4:187846200-187846400	Active TSS	Fetal Brain Male	brain

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