Variant report

Variant	nsv4372
Chromosome Location	chr4:69764499-69810115
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:389)
CpG islands
(count:122)
Chromatin interactive
region (count:8)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:389 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:69773623-69773956	HepG2	liver:	n/a	n/a
2	ATF2	chr4:69771421-69772394	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF2	chr4:69771508-69772440	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr4:69772001-69772532	H1-hESC	embryonic stem cell:	n/a	n/a
5	BCL11A	chr4:69771616-69771818	H1-hESC	embryonic stem cell:	n/a	n/a
6	BCL11A	chr4:69771517-69771820	H1-hESC	embryonic stem cell:	n/a	n/a
7	BCL3	chr4:69773519-69774111	A549	lung:	n/a	n/a
8	CEBPB	chr4:69808646-69808783	K562	blood:	n/a	chr4:69808687-69808698
9	CEBPB	chr4:69808552-69808856	HepG2	liver:	n/a	chr4:69808687-69808698
10	CEBPB	chr4:69793025-69793234	A549	lung:	n/a	chr4:69793134-69793145 chr4:69793136-69793145
11	CEBPB	chr4:69773547-69773896	A549	lung:	n/a	chr4:69773655-69773666
12	CEBPB	chr4:69773544-69773708	K562	blood:	n/a	chr4:69773655-69773666
13	CEBPB	chr4:69773514-69773788	HepG2	liver:	n/a	chr4:69773655-69773666
14	CEBPB	chr4:69773510-69774044	A549	lung:	n/a	chr4:69773655-69773666
15	CEBPB	chr4:69808523-69808836	IMR90	lung:	n/a	chr4:69808687-69808698
16	CEBPB	chr4:69792975-69793305	HepG2	liver:	n/a	chr4:69793134-69793145 chr4:69793136-69793145
17	CEBPB	chr4:69770497-69770740	H1-hESC	embryonic stem cell:	n/a	n/a
18	CEBPB	chr4:69773475-69774184	A549	lung:	n/a	chr4:69773655-69773666
19	CHD1	chr4:69771227-69771760	H1-hESC	embryonic stem cell:	n/a	n/a
20	CHD2	chr4:69770494-69770785	H1-hESC	embryonic stem cell:	n/a	n/a
21	CHD2	chr4:69770434-69770964	GM12878	blood:	n/a	n/a
22	CHD2	chr4:69771319-69772937	H1-hESC	embryonic stem cell:	n/a	n/a
23	CTCF	chr4:69769240-69769390	GM12875	blood:	n/a	n/a
24	CTCF	chr4:69770503-69770697	Gliobla	brain:	n/a	n/a
25	CTCF	chr4:69770554-69770695	LNCaP	prostate:	n/a	n/a
26	CTCF	chr4:69770520-69770670	A549	lung:	n/a	n/a
27	CTCF	chr4:69770500-69770650	GM12864	blood:	n/a	n/a
28	CTCF	chr4:69768680-69768830	HepG2	liver:	n/a	n/a
29	CTCF	chr4:69770580-69770730	WERI-Rb-1	eye:	n/a	n/a
30	CTCF	chr4:69775200-69775350	GM12872	blood:	n/a	n/a
31	CTCF	chr4:69770495-69770694	MCF-7	breast:	n/a	n/a
32	CTCF	chr4:69770529-69770712	LNCaP	prostate:	n/a	n/a
33	CTCF	chr4:69804895-69804956	GM20000	blood:	n/a	n/a
34	CTCF	chr4:69770503-69770683	MCF-7	breast:	n/a	n/a
35	CTCF	chr4:69770480-69770630	HEEpiC	esophagus:	n/a	n/a
36	CTCF	chr4:69770510-69770612	SK-N-SH_RA	brain:	n/a	n/a
37	CTCF	chr4:69770540-69770679	Pancreas_OC	pancreas:	n/a	n/a
38	CTCF	chr4:69775362-69775383	GM13976	blood:	n/a	n/a
39	CTCF	chr4:69769180-69769330	GM12873	blood:	n/a	n/a
40	CTCF	chr4:69768808-69768865	K562	blood:	n/a	n/a
41	CTCF	chr4:69789400-69789550	MCF-7	breast:	n/a	n/a
42	CTCF	chr4:69770520-69770670	GM12866	blood:	n/a	n/a
43	CTCF	chr4:69770485-69770699	MCF-7	breast:	n/a	n/a
44	CTCF	chr4:69770514-69770694	Kidney_OC	kidney:	n/a	n/a
45	CTCF	chr4:69770500-69770650	HA-sp	spinal cord:	n/a	n/a
46	CTCF	chr4:69770580-69770730	GM12865	blood:	n/a	n/a
47	CTCF	chr4:69770520-69770670	AG04450	lung:	n/a	n/a
48	CTCF	chr4:69770460-69770610	HVMF	connective:	n/a	n/a
49	CTCF	chr4:69770461-69770759	HepG2	liver:	n/a	n/a
50	CTCF	chr4:69770560-69770710	HVMF	connective:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:69771757-69771807	HCT-116	colon:	n/a
2	chr4:69810056-69810106	SK-N-SH	brain:	n/a
3	chr4:69810056-69810106	NHBE	bronchial:	n/a
4	chr4:69810056-69810106	Caco-2	colon:	n/a
5	chr4:69810056-69810106	HUVEC	blood vessel:	n/a
6	chr4:69771757-69771807	HEK293	kidney:	embryo
7	chr4:69771757-69771807	Jurkat	blood:	n/a
8	chr4:69771757-69771807	HUVEC	blood vessel:	n/a
9	chr4:69771757-69771807	H1-hESC	embryonic stem cell:	embryo
10	chr4:69771757-69771807	HMEC	breast:	n/a
11	chr4:69771757-69771807	HRPEpiC	eye:	n/a
12	chr4:69771757-69771807	GM19239	blood:	n/a
13	chr4:69771757-69771807	AG09309	skin:	n/a
14	chr4:69771757-69771807	HIPEpiC	eye:	n/a
15	chr4:69810056-69810106	HCT-116	colon:	n/a
16	chr4:69771757-69771807	PFSK-1	brain:	n/a
17	chr4:69810056-69810106	HPAEpiC	pulmonary alveolar:	n/a
18	chr4:69810056-69810106	GM12878	blood:	n/a
19	chr4:69771757-69771807	AoSMC	blood vessel:	n/a
20	chr4:69771757-69771807	ECC-1	luminal epithelium:	n/a
21	chr4:69810056-69810106	HepG2	liver:	n/a
22	chr4:69771757-69771807	HCM	heart:	n/a
23	chr4:69810056-69810106	U87	brain:	n/a
24	chr4:69771757-69771807	MCF-7	breast:	n/a
25	chr4:69810056-69810106	ProgFib	skin:	n/a
26	chr4:69771757-69771807	AG10803	skin:	n/a
27	chr4:69810056-69810106	AoSMC	blood vessel:	n/a
28	chr4:69810056-69810106	BE2_C	brain:	n/a
29	chr4:69771757-69771807	GM06990	blood:	n/a
30	chr4:69810056-69810106	BJ	skin:	n/a
31	chr4:69810056-69810106	AG09309	skin:	n/a
32	chr4:69771757-69771807	Caco-2	colon:	n/a
33	chr4:69810056-69810106	NHDF-neo	bronchial:	n/a
34	chr4:69810056-69810106	GM12891	blood:	n/a
35	chr4:69810056-69810106	AG10803	skin:	n/a
36	chr4:69810056-69810106	AG09319	gingival:	n/a
37	chr4:69810056-69810106	SK-N-MC	brain:	n/a
38	chr4:69771757-69771807	NT2-D1	testis:	n/a
39	chr4:69771757-69771807	SK-N-SH_RA	brain:	n/a
40	chr4:69771757-69771807	BJ	skin:	n/a
41	chr4:69771757-69771807	K562	blood:	n/a
42	chr4:69771757-69771807	NB4	blood:	n/a
43	chr4:69771757-69771807	Hepatocyte	liver:	n/a
44	chr4:69810056-69810106	H1-hESC	embryonic stem cell:	embryo
45	chr4:69810056-69810106	HEK293	kidney:	embryo
46	chr4:69810056-69810106	HEEpiC	esophagus:	n/a
47	chr4:69810056-69810106	SAEC	small airway:	n/a
48	chr4:69810056-69810106	K562	blood:	n/a
49	chr4:69771757-69771807	NH-A	brain:	n/a
50	chr4:69810056-69810106	GM19239	blood:	n/a

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:35451886..35454032-chr4:69771560..69773312,2	MCF-7	breast:
2	chr4:69778943..69780754-chr4:69782695..69784707,2	MCF-7	breast:
3	chr14:35810366..35811287-chr4:69770665..69771581,2	MCF-7	breast:
4	chr4:69778943..69780754-chr4:69782695..69784707,2	MCF-7	breast:
5	chr4:69730313..69732082-chr4:69762356..69764791,2	MCF-7	breast:
6	chr4:69770351..69773308-chr4:69775332..69780038,5	MCF-7	breast:
7	chr4:69213512..69216500-chr4:69770884..69773457,2	MCF-7	breast:
8	chr4:69755920..69758085-chr4:69768537..69771437,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-UGT2A3-4	chr4:69772593-69772701	ENSG00000272626.1
2	lnc-UGT2A3-4	chr4:69766726-69767093	ENSG00000272626.1

No data

Variant related genes	Relation type
ENSG00000272626	TF binding region
ENSG00000249985	TF binding region
ENSG00000248613	TF binding region
ENSG00000198277	TF binding region
ENSG00000272626	CpG island
ENSG00000249985	CpG island
ENSG00000248613	CpG island
ENSG00000198277	CpG island
ENSG00000272626	chromatin interactions
ENSG00000100883	chromatin interactions
ENSG00000083896	chromatin interactions

Extended variants
information (count: 1781 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:1781 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10021345	chr4:69764517-69764518	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs563909717	chr4:69764569-69764570	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs532186931	chr4:69764653-69764654	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs532937233	chr4:69764666-69764667	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs546523142	chr4:69764673-69764674	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs566418868	chr4:69764747-69764748	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs539441627	chr4:69764786-69764787	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs376043162	chr4:69764811-69764812	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs548916226	chr4:69764880-69764881	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs115805235	chr4:69764890-69764891	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs185418294	chr4:69764893-69764894	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs536070512	chr4:69765003-69765004	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs557611763	chr4:69765048-69765049	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs7686427	chr4:69765078-69765079	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs369655014	chr4:69765091-69765092	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs540024454	chr4:69765104-69765105	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs191099142	chr4:69765126-69765127	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs553745898	chr4:69765130-69765131	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs555508096	chr4:69765148-69765149	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs548193990	chr4:69765188-69765189	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs139762577	chr4:69765209-69765210	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs541864641	chr4:69765225-69765226	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs562076692	chr4:69765248-69765249	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs575668139	chr4:69765263-69765264	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs112450979	chr4:69765281-69765282	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs181134387	chr4:69765282-69765283	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs533000044	chr4:69765350-69765351	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs146129227	chr4:69765440-69765441	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs186575701	chr4:69765452-69765453	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs553438167	chr4:69765489-69765490	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs529146051	chr4:69765501-69765502	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs76949806	chr4:69765512-69765513	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs568807946	chr4:69765534-69765535	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs545428538	chr4:69765549-69765550	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs551536808	chr4:69765559-69765560	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs571356924	chr4:69765568-69765569	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs540088161	chr4:69765597-69765598	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs553561019	chr4:69765654-69765655	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs191578104	chr4:69765685-69765686	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs536116166	chr4:69765687-69765688	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs140110941	chr4:69765704-69765705	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs142395507	chr4:69765728-69765729	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs1531251	chr4:69765734-69765735	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs557876139	chr4:69765745-69765746	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs1531250	chr4:69765764-69765765	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs562821848	chr4:69765768-69765769	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs540047271	chr4:69765779-69765780	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs115558925	chr4:69765782-69765783	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs76101937	chr4:69765795-69765796	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs142624255	chr4:69765800-69765801	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:81)

Disease	PMID	Source
Gastrointestinal stromal cancer	16982739	CNVD
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
Non-small cell lung cancer	21829676	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Lung cancer	18438408	CNVD
Breast cancer	17603634	CNVD
Glioblastoma multiforme	21922591	CNVD
Parkinson disease	21956041	CNVD
Mental retardation	20522426	CNVD
delayed speech	20522426	CNVD
growth disorder	20522426	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
Multiple myeloma	16616336	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
Colorectal cancer	16272173	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16573809	CNVD
Osteoporosis	18992858	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Myelodysplastic syndrome	21251322	CNVD
Multiple myeloma	17550852	CNVD
Graft versus host disease	20877625	CNVD
Breast cancer	21990379	CNVD
Myelofibrosis	22110671	CNVD
Osteoporosis	20877625	CNVD
Osteoporosis	19737800	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Glioblastoma multiforme	21138945	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:323 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:69762000-69769400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr4:69763200-69764600	Weak transcription	Liver	Liver
3	chr4:69763200-69769400	Weak transcription	Pancreas	Pancrea
4	chr4:69763200-69770200	Weak transcription	Fetal Intestine Large	intestine
5	chr4:69764000-69766400	Weak transcription	Fetal Intestine Small	intestine
6	chr4:69764600-69766000	Enhancers	Liver	Liver
7	chr4:69765000-69770400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
8	chr4:69766000-69766400	Weak transcription	Liver	Liver
9	chr4:69766000-69769800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr4:69766400-69766600	Enhancers	Liver	Liver
11	chr4:69766400-69767800	Strong transcription	Fetal Intestine Small	intestine
12	chr4:69766600-69769600	Weak transcription	Liver	Liver
13	chr4:69767600-69768400	Enhancers	HepG2	liver
14	chr4:69767800-69768000	Weak transcription	Fetal Intestine Small	intestine
15	chr4:69768000-69768600	Enhancers	Fetal Intestine Small	intestine
16	chr4:69768400-69770400	Weak transcription	HepG2	liver
17	chr4:69768600-69769400	Weak transcription	Fetal Intestine Small	intestine
18	chr4:69769400-69769800	Enhancers	Pancreas	Pancrea
19	chr4:69769400-69770200	Enhancers	Fetal Intestine Small	intestine
20	chr4:69769400-69773400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
21	chr4:69769600-69769800	Enhancers	Liver	Liver
22	chr4:69769600-69770400	Enhancers	Stomach Mucosa	stomach
23	chr4:69769600-69771000	Active TSS	Duodenum Mucosa	Duodenum
24	chr4:69769600-69771600	Enhancers	H1 Cell Line	embryonic stem cell
25	chr4:69769600-69773200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
26	chr4:69769800-69770000	Flanking Active TSS	Pancreas	Pancrea
27	chr4:69769800-69770400	Flanking Active TSS	Liver	Liver
28	chr4:69769800-69770800	Enhancers	iPS-18 Cell Line	embryonic stem cell
29	chr4:69769800-69771000	Enhancers	HUES6 Cell Line	embryonic stem cell
30	chr4:69769800-69771000	Enhancers	HUES64 Cell Line	embryonic stem cell
31	chr4:69769800-69771600	Enhancers	Cortex derived primary cultured neurospheres	brain
32	chr4:69769800-69772200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
33	chr4:69769800-69772400	Enhancers	Placenta	Placenta
34	chr4:69770000-69770200	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
35	chr4:69770000-69770200	Enhancers	Rectal Mucosa Donor 31	rectum
36	chr4:69770000-69770400	Enhancers	Breast Myoepithelial Primary Cells	Breast
37	chr4:69770000-69770400	Enhancers	Duodenum Smooth Muscle	Duodenum
38	chr4:69770000-69770800	Enhancers	ES-I3 Cell Line	embryonic stem cell
39	chr4:69770000-69770800	Active TSS	Pancreas	Pancrea
40	chr4:69770000-69771000	Enhancers	iPS-20b Cell Line	embryonic stem cell
41	chr4:69770000-69771000	Active TSS	Brain Inferior Temporal Lobe	brain
42	chr4:69770000-69771000	Active TSS	Stomach Smooth Muscle	stomach
43	chr4:69770000-69771200	Enhancers	H9 Cell Line	embryonic stem cell
44	chr4:69770000-69771200	Enhancers	HUES48 Cell Line	embryonic stem cell
45	chr4:69770000-69772200	Active TSS	Rectal Smooth Muscle	rectum
46	chr4:69770000-69773000	Active TSS	Pancreatic Islets	Pancreatic Islet
47	chr4:69770200-69770400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
48	chr4:69770200-69770400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
49	chr4:69770200-69770400	Enhancers	Fetal Intestine Large	intestine
50	chr4:69770200-69770800	Active TSS	Brain Substantia Nigra	brain

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links