Variant report

Variant	nsv879527
Chromosome Location	chr4:88194170-88250203
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:370)
CpG islands
(count:366)
Chromatin interactive
region (count:19)
LncRNA
region (count:2)
Mature miRNA
region (count: 1)
miRNA target
sites (count:0)

(count:370 , 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	chr4:88238747-88239287	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:88199339-88199978	HepG2	liver:	n/a	n/a
3	ARID3A	chr4:88195615-88195678	HepG2	liver:	n/a	n/a
4	ARID3A	chr4:88196507-88196704	HepG2	liver:	n/a	n/a
5	ATF2	chr4:88227219-88227557	GM12878	blood:	n/a	n/a
6	ATF2	chr4:88227105-88227643	GM12878	blood:	n/a	n/a
7	ATF3	chr4:88199339-88199930	HepG2	liver:	n/a	n/a
8	ATF3	chr4:88223744-88223892	K562	blood:	n/a	n/a
9	ATF3	chr4:88199549-88199769	HepG2	liver:	n/a	n/a
10	BATF	chr4:88228029-88228308	GM12878	blood:	n/a	n/a
11	BATF	chr4:88227243-88227499	GM12878	blood:	n/a	chr4:88227386-88227397
12	BCL3	chr4:88225796-88226325	A549	lung:	n/a	n/a
13	BCL3	chr4:88227213-88227544	GM12878	blood:	n/a	n/a
14	BHLHE40	chr4:88238776-88238949	HepG2	liver:	n/a	n/a
15	BHLHE40	chr4:88199328-88199876	HepG2	liver:	n/a	n/a
16	BHLHE40	chr4:88199420-88199720	HepG2	liver:	n/a	n/a
17	BHLHE40	chr4:88199507-88199750	HepG2	liver:	n/a	n/a
18	BRCA1	chr4:88225715-88226363	Hela-S3	cervix:	n/a	n/a
19	CBX3	chr4:88215016-88215405	K562	blood:	n/a	n/a
20	CBX3	chr4:88207920-88208188	K562	blood:	n/a	n/a
21	CEBPB	chr4:88241858-88242058	K562	blood:	n/a	chr4:88241967-88241980 chr4:88241967-88241978
22	CEBPB	chr4:88246787-88246815	IMR90	lung:	n/a	n/a
23	CEBPB	chr4:88246514-88246851	MCF-7	breast:	n/a	n/a
24	CEBPB	chr4:88238773-88238946	HepG2	liver:	n/a	n/a
25	CEBPB	chr4:88225791-88226474	MCF-7	breast:	n/a	n/a
26	CEBPB	chr4:88238667-88239136	MCF-7	breast:	n/a	n/a
27	CEBPB	chr4:88238743-88239106	MCF-7	breast:	n/a	n/a
28	CEBPB	chr4:88238721-88239017	A549	lung:	n/a	n/a
29	CEBPB	chr4:88238687-88239062	HepG2	liver:	n/a	n/a
30	CEBPB	chr4:88249280-88249561	HepG2	liver:	n/a	chr4:88249401-88249412
31	CEBPB	chr4:88197413-88197511	HepG2	liver:	n/a	chr4:88197420-88197431
32	CEBPB	chr4:88225700-88226496	Hela-S3	cervix:	n/a	n/a
33	CEBPB	chr4:88238754-88238999	IMR90	lung:	n/a	n/a
34	CEBPB	chr4:88222901-88223173	A549	lung:	n/a	chr4:88223035-88223046
35	CEBPB	chr4:88222884-88223200	IMR90	lung:	n/a	chr4:88223035-88223046
36	CEBPB	chr4:88195585-88195771	HepG2	liver:	n/a	n/a
37	CEBPB	chr4:88222910-88223189	K562	blood:	n/a	chr4:88223035-88223046
38	CEBPB	chr4:88238169-88239081	Hela-S3	cervix:	n/a	n/a
39	CEBPB	chr4:88222879-88223179	HepG2	liver:	n/a	chr4:88223035-88223046
40	CEBPB	chr4:88226731-88227502	Hela-S3	cervix:	n/a	n/a
41	CEBPB	chr4:88230065-88230288	Hela-S3	cervix:	n/a	n/a
42	CEBPB	chr4:88199523-88199974	HepG2	liver:	n/a	n/a
43	CEBPB	chr4:88238650-88239170	A549	lung:	n/a	n/a
44	CEBPB	chr4:88238748-88239007	A549	lung:	n/a	n/a
45	CEBPB	chr4:88241820-88242139	HepG2	liver:	n/a	chr4:88241967-88241980 chr4:88241967-88241978
46	CEBPD	chr4:88238790-88238923	HepG2	liver:	n/a	n/a
47	CREB1	chr4:88227197-88227666	GM12878	blood:	n/a	n/a
48	CTCF	chr4:88231972-88232092	HepG2	liver:	n/a	n/a
49	CTCF	chr4:88207876-88207941	GM13976	blood:	n/a	n/a
50	CTCF	chr4:88236142-88236207	Lung_OC	lung:	n/a	n/a

(count:366 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:88233933-88233983	AG09319	gingival:	n/a
2	chr4:88244142-88244192	HEEpiC	esophagus:	n/a
3	chr4:88244909-88244959	HAEpiC	amniotic membrane:	n/a
4	chr4:88244909-88244959	BE2_C	brain:	n/a
5	chr4:88244909-88244959	PANC-1	pancreas:	n/a
6	chr4:88244142-88244192	U87	brain:	n/a
7	chr4:88245032-88245082	NH-A	brain:	n/a
8	chr4:88245032-88245082	SK-N-SH	brain:	n/a
9	chr4:88244142-88244192	T-47D	breast:	n/a
10	chr4:88245032-88245082	NB4	blood:	n/a
11	chr4:88243818-88243868	PFSK-1	brain:	n/a
12	chr4:88244142-88244192	HPAEpiC	pulmonary alveolar:	n/a
13	chr4:88233933-88233983	HL-60	blood:	n/a
14	chr4:88244909-88244959	PFSK-1	brain:	n/a
15	chr4:88244142-88244192	Hela-S3	cervix:	n/a
16	chr4:88225834-88225884	HEEpiC	esophagus:	n/a
17	chr4:88244909-88244959	AG10803	skin:	n/a
18	chr4:88244142-88244192	SK-N-SH	brain:	n/a
19	chr4:88245032-88245082	PrEC	prostate:	n/a
20	chr4:88244142-88244192	NB4	blood:	n/a
21	chr4:88243818-88243868	K562	blood:	n/a
22	chr4:88244909-88244959	HPAEpiC	pulmonary alveolar:	n/a
23	chr4:88244909-88244959	Jurkat	blood:	n/a
24	chr4:88243818-88243868	MCF10A-Er-Src	breast:	n/a
25	chr4:88225834-88225884	NB4	blood:	n/a
26	chr4:88245032-88245082	LNCaP	prostate:	n/a
27	chr4:88225834-88225884	AG09319	gingival:	n/a
28	chr4:88233933-88233983	HNPCEpiC	eye:	n/a
29	chr4:88244909-88244959	AG09319	gingival:	n/a
30	chr4:88233933-88233983	HepG2	liver:	n/a
31	chr4:88225834-88225884	GM06990	blood:	n/a
32	chr4:88245032-88245082	SAEC	small airway:	n/a
33	chr4:88225834-88225884	Hela-S3	cervix:	n/a
34	chr4:88244909-88244959	NH-A	brain:	n/a
35	chr4:88243818-88243868	AG10803	skin:	n/a
36	chr4:88243818-88243868	SKMC	muscle:	n/a
37	chr4:88225834-88225884	HNPCEpiC	eye:	n/a
38	chr4:88225834-88225884	BE2_C	brain:	n/a
39	chr4:88243818-88243868	T-47D	breast:	n/a
40	chr4:88244142-88244192	HRE	kidney:	n/a
41	chr4:88225834-88225884	SKMC	muscle:	n/a
42	chr4:88244909-88244959	SK-N-SH_RA	brain:	n/a
43	chr4:88244909-88244959	AG04450	lung:	fetal
44	chr4:88245032-88245082	HRE	kidney:	n/a
45	chr4:88243818-88243868	AoSMC	blood vessel:	n/a
46	chr4:88233933-88233983	HCM	heart:	n/a
47	chr4:88244142-88244192	HCT-116	colon:	n/a
48	chr4:88225834-88225884	GM12891	blood:	n/a
49	chr4:88245032-88245082	Jurkat	blood:	n/a
50	chr4:88245032-88245082	H1-hESC	embryonic stem cell:	embryo

(count:19 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:88216757..88219177-chr4:88220101..88221682,2	MCF-7	breast:
2	chr4:88225790..88227669-chr4:88236912..88239118,2	MCF-7	breast:
3	chr4:88241962..88245128-chr4:88247108..88249633,3	MCF-7	breast:
4	chr4:88224415..88227242-chr4:88231505..88233396,2	K562	blood:
5	chr4:88224415..88227242-chr4:88231505..88233396,2	K562	blood:
6	chr4:88225793..88228433-chr4:88233021..88235909,2	MCF-7	breast:
7	chr4:88237707..88239445-chr4:88243261..88245305,2	MCF-7	breast:
8	chr10:46970031..46970993-chr4:88194361..88194882,2	MCF-7	breast:
9	chr4:88187820..88189394-chr4:88231187..88233154,2	MCF-7	breast:
10	chr4:88242503..88244047-chr4:88248462..88250419,2	K562	blood:
11	chr4:88242496..88244669-chr4:88248333..88250976,2	MCF-7	breast:
12	chr4:88225790..88227669-chr4:88236912..88239118,2	MCF-7	breast:
13	chr4:88226132..88228278-chr4:88229243..88230944,2	MCF-7	breast:
14	chr4:88216757..88219177-chr4:88220101..88221682,2	MCF-7	breast:
15	chr4:88226132..88228278-chr4:88229243..88230944,2	MCF-7	breast:
16	chr4:88229442..88232296-chr4:88234376..88236070,2	K562	blood:
17	chr4:88141337..88143545-chr4:88209433..88211061,2	MCF-7	breast:
18	chr4:88225793..88228433-chr4:88233021..88235909,2	MCF-7	breast:
19	chr4:88229442..88232296-chr4:88234376..88236070,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AFF1-1	chr4:88198781-88198895	XLOC_003601
2	lnc-AFF1-1	chr4:88199776-88199855	XLOC_003601

miRNA name	Chromosome Location	mirBase accession
hsa-miR-5705	chr4:88221657-88221679	MIMAT0022499

No data

Variant related genes	Relation type
HSD17B13	TF binding region
MIR5705	TF binding region
HSD17B13	CpG island
MIR5705	CpG island
ENSG00000204176	chromatin interactions
ENSG00000250572	chromatin interactions
ENSG00000145332	chromatin interactions
ENSG00000170509	chromatin interactions

Extended variants
information (count: 1713 )
Associated
traits (count: 85 )

Variant overlapped rSNPs/rCNVs (count:1713 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11731978	chr4:88194170-88194171	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs531749526	chr4:88194176-88194177	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs6853297	chr4:88194203-88194204	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs140577070	chr4:88194256-88194257	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs368226525	chr4:88194291-88194292	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs11732868	chr4:88194338-88194339	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs6858253	chr4:88194341-88194342	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs11724713	chr4:88194345-88194346	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs57954253	chr4:88194377-88194378	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs145699062	chr4:88194378-88194379	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs548351867	chr4:88194400-88194401	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs76782137	chr4:88194416-88194417	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs528575418	chr4:88194478-88194479	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs79652782	chr4:88194485-88194486	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs547204780	chr4:88194506-88194507	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs568575021	chr4:88194515-88194516	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs200248721	chr4:88194610-88194611	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs536029713	chr4:88194615-88194616	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs184778955	chr4:88194663-88194664	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs139650480	chr4:88194673-88194674	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs189320089	chr4:88194699-88194700	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs138172301	chr4:88194722-88194723	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs77644632	chr4:88194759-88194760	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs572921345	chr4:88194791-88194792	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs114948589	chr4:88194793-88194794	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs192366005	chr4:88194802-88194803	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs184699024	chr4:88194855-88194856	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs573522810	chr4:88194888-88194889	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs559684180	chr4:88194903-88194904	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs369872228	chr4:88194915-88194916	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs543956362	chr4:88194944-88194945	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs75802753	chr4:88195010-88195011	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs577509107	chr4:88195025-88195026	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs189567435	chr4:88195085-88195086	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs35688400	chr4:88195143-88195144	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs564302597	chr4:88195206-88195207	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs528451458	chr4:88195212-88195213	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs35242187	chr4:88195256-88195257	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs546798209	chr4:88195321-88195322	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs181414083	chr4:88195331-88195332	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs529516702	chr4:88195352-88195353	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs34749810	chr4:88195394-88195395	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs551185727	chr4:88195395-88195396	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs186044946	chr4:88195438-88195439	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs540114310	chr4:88195453-88195454	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs78405321	chr4:88195459-88195460	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs13142655	chr4:88195494-88195495	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs189191466	chr4:88195528-88195529	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs555174220	chr4:88195535-88195536	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs114907246	chr4:88195546-88195547	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:85)

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
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
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
Olfactory neuroblastoma	18408657	CNVD
small cell lung cancer	20016488	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17133270	CNVD
Colorectal cancer	20459617	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	17443227	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
Breast cancer	22522925	CNVD
Parkinson disease	20877625	CNVD
Hirschsprung''s Disease	21712996	CNVD
Congenital anomalies of the kidney and urinary tract	20505237	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Glioma	20126413	CNVD

Chromatin state (count:129 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:88192400-88196000	Weak transcription	Liver	Liver
2	chr4:88193400-88194400	Enhancers	Stomach Mucosa	stomach
3	chr4:88193600-88195400	Weak transcription	HepG2	liver
4	chr4:88194400-88196000	Weak transcription	Stomach Mucosa	stomach
5	chr4:88195400-88197000	Enhancers	HepG2	liver
6	chr4:88195800-88196400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr4:88196000-88196200	Enhancers	Fetal Intestine Large	intestine
8	chr4:88196000-88196400	Enhancers	Primary hematopoietic stem cells short term culture	blood
9	chr4:88196000-88196400	Enhancers	Liver	Liver
10	chr4:88196200-88196400	Enhancers	Stomach Mucosa	stomach
11	chr4:88196200-88196400	Bivalent Enhancer	NHDF-Ad	bronchial
12	chr4:88196200-88196600	Enhancers	Pancreatic Islets	Pancreatic Islet
13	chr4:88196400-88199200	Weak transcription	Liver	Liver
14	chr4:88197000-88198600	Weak transcription	HepG2	liver
15	chr4:88198600-88200800	Enhancers	HepG2	liver
16	chr4:88199200-88200200	Enhancers	Liver	Liver
17	chr4:88199600-88200000	Enhancers	Pancreas	Pancrea
18	chr4:88200200-88200400	Enhancers	Aorta	Aorta
19	chr4:88200200-88200600	Weak transcription	Liver	Liver
20	chr4:88200400-88201000	Weak transcription	Aorta	Aorta
21	chr4:88200600-88200800	Enhancers	Liver	Liver
22	chr4:88200800-88205200	Weak transcription	Liver	Liver
23	chr4:88205200-88205600	Enhancers	Liver	Liver
24	chr4:88205800-88206000	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
25	chr4:88207800-88208400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
26	chr4:88208000-88208200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
27	chr4:88220800-88221400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
28	chr4:88221000-88221400	Enhancers	Liver	Liver
29	chr4:88221000-88221400	Enhancers	Fetal Lung	lung
30	chr4:88221400-88225400	Weak transcription	Liver	Liver
31	chr4:88221400-88225800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
32	chr4:88224000-88225600	Enhancers	Hela-S3	cervix
33	chr4:88225400-88237800	Strong transcription	Liver	Liver
34	chr4:88225600-88225800	Flanking Active TSS	Hela-S3	cervix
35	chr4:88225600-88225800	Enhancers	NHEK	skin
36	chr4:88225800-88226000	Enhancers	Osteobl	bone
37	chr4:88225800-88226200	Flanking Active TSS	NHEK	skin
38	chr4:88225800-88226400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr4:88225800-88226400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
40	chr4:88225800-88227200	Active TSS	Hela-S3	cervix
41	chr4:88226000-88226600	Active TSS	A549	lung
42	chr4:88226200-88226600	Active TSS	Aorta	Aorta
43	chr4:88226200-88226800	Active TSS	NHEK	skin
44	chr4:88226400-88231600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr4:88226600-88227000	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
46	chr4:88226600-88229000	Weak transcription	A549	lung
47	chr4:88226800-88227200	Flanking Active TSS	NHEK	skin
48	chr4:88227000-88229000	Enhancers	Stomach Mucosa	stomach
49	chr4:88227200-88227600	Flanking Active TSS	Hela-S3	cervix
50	chr4:88227600-88228400	Enhancers	Hela-S3	cervix

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