Variant report

Variant	nsv879561
Chromosome Location	chr4:92005403-92061748
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:92034335-92034619	HepG2	liver:	n/a	n/a
2	BACH1	chr4:92007259-92007496	H1-hESC	embryonic stem cell:	n/a	n/a
3	BCL11A	chr4:92010407-92010604	GM12878	blood:	n/a	n/a
4	BCL11A	chr4:92010328-92010676	GM12878	blood:	n/a	n/a
5	CBX3	chr4:92024996-92025295	K562	blood:	n/a	n/a
6	CEBPB	chr4:92007232-92007488	H1-hESC	embryonic stem cell:	n/a	n/a
7	CEBPB	chr4:92044571-92044854	HepG2	liver:	n/a	chr4:92044758-92044769 chr4:92044718-92044729
8	CEBPB	chr4:92044617-92044895	A549	lung:	n/a	chr4:92044758-92044769 chr4:92044718-92044729
9	CEBPB	chr4:92044637-92044818	H1-hESC	embryonic stem cell:	n/a	chr4:92044758-92044769 chr4:92044718-92044729
10	CEBPB	chr4:92034320-92034601	ECC-1	luminal epithelium:	n/a	n/a
11	CEBPZ	chr4:92031768-92031775	HepG2	liver:	n/a	n/a
12	CTCF	chr4:92034360-92034510	A549	lung:	n/a	chr4:92034457-92034478 chr4:92034455-92034473 chr4:92034456-92034472
13	CTCF	chr4:92025594-92025679	GM20000	blood:	n/a	n/a
14	CTCF	chr4:92014053-92014141	Medullo	brain:	n/a	n/a
15	CTCF	chr4:92034420-92034570	GM12872	blood:	n/a	chr4:92034457-92034478 chr4:92034455-92034473 chr4:92034456-92034472
16	CTCF	chr4:92013960-92014110	MCF-7	breast:	n/a	n/a
17	CTCF	chr4:92034380-92034530	MCF-7	breast:	n/a	chr4:92034457-92034478 chr4:92034455-92034473 chr4:92034456-92034472
18	CTCF	chr4:92038160-92038310	HepG2	liver:	n/a	chr4:92038207-92038228
19	CTCF	chr4:92034420-92034570	WERI-Rb-1	eye:	n/a	chr4:92034457-92034478 chr4:92034455-92034473 chr4:92034456-92034472
20	CTCF	chr4:92034360-92034510	HPF	lung:	n/a	chr4:92034457-92034478 chr4:92034455-92034473 chr4:92034456-92034472
21	CTCF	chr4:92034380-92034530	HepG2	liver:	n/a	chr4:92034457-92034478 chr4:92034455-92034473 chr4:92034456-92034472
22	CTCF	chr4:92034360-92034510	HCM	heart:	n/a	chr4:92034457-92034478 chr4:92034455-92034473 chr4:92034456-92034472
23	CTCF	chr4:92034378-92034549	GM13976	blood:	n/a	chr4:92034457-92034478 chr4:92034455-92034473 chr4:92034456-92034472
24	CTCF	chr4:92034333-92034649	H1-hESC	embryonic stem cell:	n/a	chr4:92034457-92034478 chr4:92034455-92034473 chr4:92034456-92034472
25	CTCF	chr4:92034380-92034530	HMEC	breast:	n/a	chr4:92034457-92034478 chr4:92034455-92034473 chr4:92034456-92034472
26	CTCF	chr4:92034380-92034530	BE2_C	brain:	n/a	chr4:92034457-92034478 chr4:92034455-92034473 chr4:92034456-92034472
27	CTCF	chr4:92038100-92038250	MCF-7	breast:	n/a	chr4:92038207-92038228
28	CTCF	chr4:92038160-92038310	SAEC	small airway:	n/a	chr4:92038207-92038228
29	CTCF	chr4:92034300-92034450	GM12869	blood:	n/a	n/a
30	CTCF	chr4:92038000-92038270	GM06990	blood:	n/a	chr4:92038207-92038228
31	CTCF	chr4:92037880-92038030	HCM	heart:	n/a	n/a
32	CTCF	chr4:92034360-92034510	HEK293	kidney:	n/a	chr4:92034457-92034478 chr4:92034455-92034473 chr4:92034456-92034472
33	CTCF	chr4:92034380-92034530	AG04449	skin:	n/a	chr4:92034457-92034478 chr4:92034455-92034473 chr4:92034456-92034472
34	CTCF	chr4:92034249-92034640	HepG2	liver:	n/a	chr4:92034457-92034478 chr4:92034455-92034473 chr4:92034456-92034472
35	CTCF	chr4:92038140-92038290	Caco-2	colon:	n/a	chr4:92038207-92038228
36	CTCF	chr4:92034360-92034510	HAc	cerebellar:	n/a	chr4:92034457-92034478 chr4:92034455-92034473 chr4:92034456-92034472
37	CTCF	chr4:92034420-92034570	AG09309	skin:	n/a	chr4:92034457-92034478 chr4:92034455-92034473 chr4:92034456-92034472
38	CTCF	chr4:92013940-92014090	RPTEC	kidney:	n/a	n/a
39	CTCF	chr4:92038140-92038290	HMF	breast:	n/a	chr4:92038207-92038228
40	CTCF	chr4:92034420-92034570	HFF	foreskin:	n/a	chr4:92034457-92034478 chr4:92034455-92034473 chr4:92034456-92034472
41	CTCF	chr4:92013861-92013912	Lung_OC	lung:	n/a	n/a
42	CTCF	chr4:92038100-92038250	GM12869	blood:	n/a	chr4:92038207-92038228
43	CTCF	chr4:92014001-92014112	A549	lung:	n/a	n/a
44	CTCF	chr4:92034380-92034530	GM12869	blood:	n/a	chr4:92034457-92034478 chr4:92034455-92034473 chr4:92034456-92034472
45	CTCF	chr4:92034335-92034569	LNCaP	prostate:	n/a	chr4:92034457-92034478 chr4:92034455-92034473 chr4:92034456-92034472
46	CTCF	chr4:92034323-92034603	Gliobla	brain:	n/a	chr4:92034457-92034478 chr4:92034455-92034473 chr4:92034456-92034472
47	CTCF	chr4:92038040-92038190	RPTEC	kidney:	n/a	n/a
48	CTCF	chr4:92014016-92014118	HUVEC	blood vessel:	n/a	n/a
49	CTCF	chr4:92034360-92034510	HRE	kidney:	n/a	chr4:92034457-92034478 chr4:92034455-92034473 chr4:92034456-92034472
50	CTCF	chr4:92014000-92014150	HA-sp	spinal cord:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:92034737-92034787	PrEC	prostate:	n/a
2	chr4:92034737-92034787	PrEC	prostate:	n/a
3	chr4:92034737-92034787	HAEpiC	amniotic membrane:	n/a
4	chr4:92048256-92048306	LNCaP	prostate:	n/a
5	chr4:92048256-92048306	AG04449	skin:	fetal
6	chr4:92034737-92034787	HMEC	breast:	n/a
7	chr4:92008475-92008525	NH-A	brain:	n/a
8	chr4:92048256-92048306	AG09309	skin:	n/a
9	chr4:92048256-92048306	HRCEpiC	kidney:	n/a
10	chr4:92008475-92008525	H1-hESC	embryonic stem cell:	embryo
11	chr4:92034737-92034787	ECC-1	luminal epithelium:	n/a
12	chr4:92034737-92034787	HEEpiC	esophagus:	n/a
13	chr4:92034737-92034787	GM06990	blood:	n/a
14	chr4:92034737-92034787	HCPEpiC	choroid plexus:	n/a
15	chr4:92008475-92008525	HCPEpiC	choroid plexus:	n/a
16	chr4:92048256-92048306	SK-N-MC	brain:	n/a
17	chr4:92034737-92034787	AoSMC	blood vessel:	n/a
18	chr4:92008475-92008525	NHBE	bronchial:	n/a
19	chr4:92008475-92008525	HMEC	breast:	n/a
20	chr4:92008475-92008525	Jurkat	blood:	n/a
21	chr4:92008475-92008525	GM12892	blood:	n/a
22	chr4:92048256-92048306	NHBE	bronchial:	n/a
23	chr4:92034737-92034787	Jurkat	blood:	n/a
24	chr4:92048256-92048306	HRPEpiC	eye:	n/a
25	chr4:92034737-92034787	GM12891	blood:	n/a
26	chr4:92008475-92008525	AG09309	skin:	n/a
27	chr4:92048256-92048306	HCPEpiC	choroid plexus:	n/a
28	chr4:92048256-92048306	SK-N-SH	brain:	n/a
29	chr4:92008475-92008525	K562	blood:	n/a
30	chr4:92008475-92008525	AG10803	skin:	n/a
31	chr4:92034737-92034787	CMK	blood:	n/a
32	chr4:92048256-92048306	HUVEC	blood vessel:	n/a
33	chr4:92008475-92008525	GM19239	blood:	n/a
34	chr4:92048256-92048306	GM12891	blood:	n/a
35	chr4:92034737-92034787	Hela-S3	cervix:	n/a
36	chr4:92048256-92048306	HCM	heart:	n/a
37	chr4:92048256-92048306	HCT-116	colon:	n/a
38	chr4:92008475-92008525	HRCEpiC	kidney:	n/a
39	chr4:92048256-92048306	SK-N-SH_RA	brain:	n/a
40	chr4:92048256-92048306	RPTEC	kidney:	n/a
41	chr4:92048256-92048306	U87	brain:	n/a
42	chr4:92008475-92008525	GM12878	blood:	n/a
43	chr4:92008475-92008525	SK-N-MC	brain:	n/a
44	chr4:92048256-92048306	AG04450	lung:	fetal
45	chr4:92034737-92034787	HRCEpiC	kidney:	n/a
46	chr4:92034737-92034787	IMR90	lung:	fetal
47	chr4:92008475-92008525	SAEC	small airway:	n/a
48	chr4:92048256-92048306	PrEC	prostate:	n/a
49	chr4:92034737-92034787	ovcar-3	ovarian:	n/a
50	chr4:92048256-92048306	BE2_C	brain:	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr4:92034306..92035417-chr4:92423226..92424074,5	MCF-7	breast:
2	chr10:82295674..82298297-chr4:92009865..92012633,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-763F8.1.1-1	chr4:92033750-92033941	ENSG00000248984.1
2	lnc-RP11-763F8.1.1-1	chr4:92029174-92029251	ENSG00000248984.1

Variant related genes	Relation type
ENSG00000248984	TF binding region
ENSG00000248984	CpG island
ENSG00000226659	chromatin interactions
ENSG00000178217	chromatin interactions

Extended variants
information (count: 1230 )
Associated
traits (count: 88 )

Variant overlapped rSNPs/rCNVs (count:1230 , 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	rs564353611	chr4:92006035-92006036	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs191771088	chr4:92006066-92006067	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs547553576	chr4:92006077-92006078	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs184558937	chr4:92006136-92006137	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs528493702	chr4:92006143-92006144	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs56340424	chr4:92006187-92006188	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs376370900	chr4:92006221-92006222	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs546747271	chr4:92006258-92006259	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs11378537	chr4:92006259-92006260	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs547156713	chr4:92006286-92006287	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs562920288	chr4:92006323-92006324	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs535349640	chr4:92006343-92006344	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs554830991	chr4:92006380-92006381	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs568673804	chr4:92006409-92006410	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs536331964	chr4:92006419-92006420	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs556342962	chr4:92006423-92006424	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs576099525	chr4:92006424-92006425	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs192881804	chr4:92006474-92006475	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs558524389	chr4:92006494-92006495	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs137927777	chr4:92006509-92006510	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs72669204	chr4:92006521-92006522	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs560909099	chr4:92006538-92006539	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs529865223	chr4:92006563-92006564	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs543505931	chr4:92006568-92006569	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs563481216	chr4:92006581-92006582	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs74328031	chr4:92006601-92006602	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs552124782	chr4:92006605-92006606	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs559712735	chr4:92006617-92006618	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs566045222	chr4:92006632-92006633	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs548893555	chr4:92006712-92006713	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs189372595	chr4:92006727-92006728	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs550916340	chr4:92006729-92006730	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs569416465	chr4:92006745-92006746	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs180986738	chr4:92006780-92006781	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs77128123	chr4:92006784-92006785	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs552045172	chr4:92006828-92006829	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs145749139	chr4:92006852-92006853	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs570390876	chr4:92006865-92006866	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs201533834	chr4:92006922-92006923	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs10584718	chr4:92006923-92006924	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs76394064	chr4:92006924-92006925	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs397771208	chr4:92006928-92006929	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs558230692	chr4:92006932-92006933	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs572039863	chr4:92006935-92006936	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs534590332	chr4:92006946-92006947	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs554893884	chr4:92006959-92006960	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs183840639	chr4:92006974-92006975	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs6842235	chr4:92006984-92006985	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs115266596	chr4:92006997-92006998	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs7685222	chr4:92006998-92006999	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:88)

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
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myxofibrosarcoma	16751306	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Parkinson disease	18923514	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	CNVD
Breast cancer	16272173	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
Adenoid cystic carcinoma	18698036	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Myelodysplastic syndrome	21251322	CNVD
Multiple myeloma	17550852	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	18414403	CNVD
primary effusion lymphomas	17116491	CNVD
Mental retardation	20522426	CNVD
delayed speech	20522426	CNVD
growth disorder	20522426	CNVD
Olfactory neuroblastoma	18408657	CNVD
small cell lung cancer	20016488	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17133270	CNVD
Colorectal cancer	20459617	CNVD
Acute monocytic leukemia	16498392	CNVD
Multiple myeloma	16616336	CNVD
Esophageal adenocarcinoma	18820669	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Myelofibrosis	22110671	CNVD
Parkinson disease	20877625	CNVD
Hirschsprung''s Disease	21712996	CNVD
Congenital anomalies of the kidney and urinary tract	20505237	CNVD
Breast cancer	17393978	CNVD
Ovarian cancer	21720365	CNVD
Obesity	20622171	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Cancer	20164920	CNVD
Cancer	20164919	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Esophageal cancer	21851588	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:92 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:92006000-92007200	Enhancers	HUES48 Cell Line	embryonic stem cell
2	chr4:92006000-92007400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
3	chr4:92006400-92007200	Enhancers	iPS-20b Cell Line	embryonic stem cell
4	chr4:92006400-92010000	Enhancers	HUES64 Cell Line	embryonic stem cell
5	chr4:92006600-92007600	Enhancers	Fetal Brain Female	brain
6	chr4:92006600-92009200	Enhancers	iPS-18 Cell Line	embryonic stem cell
7	chr4:92006600-92009400	Enhancers	iPS-15b Cell Line	embryonic stem cell
8	chr4:92006800-92007400	Enhancers	HUES6 Cell Line	embryonic stem cell
9	chr4:92006800-92007600	Enhancers	H1 Cell Line	embryonic stem cell
10	chr4:92006800-92007800	Enhancers	ES-I3 Cell Line	embryonic stem cell
11	chr4:92006800-92008400	Enhancers	Fetal Lung	lung
12	chr4:92007200-92007600	Active TSS	HUES48 Cell Line	embryonic stem cell
13	chr4:92007200-92007600	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
14	chr4:92007200-92007600	Enhancers	Brain Germinal Matrix	brain
15	chr4:92007400-92008600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
16	chr4:92007400-92008800	Weak transcription	HUES6 Cell Line	embryonic stem cell
17	chr4:92007600-92008000	Weak transcription	H1 Cell Line	embryonic stem cell
18	chr4:92007600-92008400	Enhancers	HUES48 Cell Line	embryonic stem cell
19	chr4:92007600-92010000	Enhancers	iPS-20b Cell Line	embryonic stem cell
20	chr4:92008000-92008200	Enhancers	H1 Cell Line	embryonic stem cell
21	chr4:92008200-92009200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
22	chr4:92008200-92010200	Weak transcription	H1 Cell Line	embryonic stem cell
23	chr4:92008400-92008600	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
24	chr4:92008600-92008800	Enhancers	HUES48 Cell Line	embryonic stem cell
25	chr4:92008600-92009400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
26	chr4:92008800-92009000	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
27	chr4:92008800-92009000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
28	chr4:92008800-92009400	Enhancers	HUES6 Cell Line	embryonic stem cell
29	chr4:92009000-92010400	Enhancers	HUES48 Cell Line	embryonic stem cell
30	chr4:92009200-92010200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
31	chr4:92009400-92017200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
32	chr4:92010000-92010800	Active TSS	A549	lung
33	chr4:92010200-92010400	Enhancers	H9 Cell Line	embryonic stem cell
34	chr4:92010200-92010600	Enhancers	H1 Cell Line	embryonic stem cell
35	chr4:92010200-92010600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
36	chr4:92010400-92010600	Enhancers	Esophagus	oesophagus
37	chr4:92010400-92010600	Enhancers	NHEK	skin
38	chr4:92010800-92014400	Weak transcription	Esophagus	oesophagus
39	chr4:92011200-92011600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
40	chr4:92011600-92012600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
41	chr4:92012600-92014600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
42	chr4:92013200-92013800	Weak transcription	NHEK	skin
43	chr4:92013400-92013600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
44	chr4:92013600-92015000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
45	chr4:92013800-92014000	Enhancers	NHEK	skin
46	chr4:92014000-92015200	Weak transcription	NHEK	skin
47	chr4:92014400-92015400	Enhancers	Esophagus	oesophagus
48	chr4:92015000-92015800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
49	chr4:92015200-92016000	Enhancers	NHEK	skin
50	chr4:92015400-92015800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin

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