Variant report

Variant	nsv1005567
Chromosome Location	chr4:98779722-99031934
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	chr4:99014048-99014354	HepG2	liver:	n/a	n/a
2	BACH1	chr4:98831268-98831463	H1-hESC	embryonic stem cell:	n/a	n/a
3	BCL3	chr4:98906959-98907234	GM12878	blood:	n/a	n/a
4	BCL3	chr4:98905816-98906082	GM12878	blood:	n/a	n/a
5	BRCA1	chr4:98908240-98908390	H1-hESC	embryonic stem cell:	n/a	n/a
6	CEBPB	chr4:98950612-98950807	HepG2	liver:	n/a	chr4:98950662-98950673
7	CEBPB	chr4:99026254-99026525	HepG2	liver:	n/a	chr4:99026390-99026401
8	CEBPB	chr4:99030855-99030922	HepG2	liver:	n/a	n/a
9	CEBPB	chr4:98989787-98989990	HepG2	liver:	n/a	chr4:98989872-98989883
10	CEBPB	chr4:99026262-99026519	IMR90	lung:	n/a	chr4:99026390-99026401
11	CEBPB	chr4:98898912-98899245	HepG2	liver:	n/a	chr4:98899094-98899105
12	CEBPB	chr4:98910863-98911031	A549	lung:	n/a	n/a
13	CEBPB	chr4:98795872-98796026	H1-hESC	embryonic stem cell:	n/a	n/a
14	CEBPB	chr4:98998918-98999191	HepG2	liver:	n/a	chr4:98999042-98999051 chr4:98999042-98999051 chr4:98999042-98999051 chr4:98999041-98999052 chr4:98999040-98999051 chr4:98999042-98999051 chr4:98999040-98999053
15	CEBPB	chr4:98863376-98863833	HCT-116	colon:	n/a	n/a
16	CEBPB	chr4:99026275-99026452	H1-hESC	embryonic stem cell:	n/a	chr4:99026390-99026401
17	CEBPB	chr4:98973085-98973241	H1-hESC	embryonic stem cell:	n/a	n/a
18	CEBPB	chr4:98849976-98850238	IMR90	lung:	n/a	n/a
19	CEBPB	chr4:99005881-99006191	HepG2	liver:	n/a	chr4:99006022-99006033
20	CEBPB	chr4:98975792-98975954	HepG2	liver:	n/a	chr4:98975918-98975929
21	CEBPB	chr4:98832733-98832877	H1-hESC	embryonic stem cell:	n/a	n/a
22	CEBPB	chr4:99005951-99006103	A549	lung:	n/a	chr4:99006022-99006033
23	CEBPB	chr4:98967948-98968326	H1-hESC	embryonic stem cell:	n/a	n/a
24	CEBPB	chr4:99005909-99006159	IMR90	lung:	n/a	chr4:99006022-99006033
25	CEBPB	chr4:98999062-98999081	K562	blood:	n/a	n/a
26	CHD2	chr4:99001733-99001756	H1-hESC	embryonic stem cell:	n/a	n/a
27	CTCF	chr4:98831240-98831390	GM12874	blood:	n/a	chr4:98831342-98831355
28	CTCF	chr4:98905860-98906010	GM12874	blood:	n/a	n/a
29	CTCF	chr4:98832843-98832881	H1-hESC	embryonic stem cell:	n/a	n/a
30	CTCF	chr4:98928080-98928230	Caco-2	colon:	n/a	n/a
31	CTCF	chr4:98831286-98831408	MCF-7	breast:	n/a	chr4:98831342-98831355
32	CTCF	chr4:98947460-98947610	MCF-7	breast:	n/a	n/a
33	CTCF	chr4:98905794-98906027	HUVEC	blood vessel:	n/a	n/a
34	CTCF	chr4:99014160-99014310	GM12872	blood:	n/a	chr4:99014180-99014201 chr4:99014185-99014203 chr4:99014186-99014202 chr4:99014192-99014199
35	CTCF	chr4:98831260-98831410	NHEK	skin:	n/a	chr4:98831342-98831355
36	CTCF	chr4:98905840-98905990	HCFaa	heart:	n/a	n/a
37	CTCF	chr4:99014100-99014250	GM12866	blood:	n/a	chr4:99014180-99014201 chr4:99014185-99014203 chr4:99014186-99014202 chr4:99014192-99014199
38	CTCF	chr4:98905875-98906003	Fibrobl	skin:	n/a	n/a
39	CTCF	chr4:99014040-99014190	BE2_C	brain:	n/a	n/a
40	CTCF	chr4:98905780-98905930	BJ	skin:	n/a	n/a
41	CTCF	chr4:99014062-99014330	HUVEC	blood vessel:	n/a	chr4:99014180-99014201 chr4:99014185-99014203 chr4:99014186-99014202 chr4:99014192-99014199
42	CTCF	chr4:98977400-98977550	SAEC	small airway:	n/a	n/a
43	CTCF	chr4:98949040-98949190	GM12873	blood:	n/a	n/a
44	CTCF	chr4:98908300-98908450	HCM	heart:	n/a	chr4:98908367-98908388 chr4:98908372-98908390
45	CTCF	chr4:98908280-98908430	WERI-Rb-1	eye:	n/a	chr4:98908367-98908388 chr4:98908372-98908390
46	CTCF	chr4:99014120-99014270	AG09309	skin:	n/a	chr4:99014180-99014201 chr4:99014185-99014203 chr4:99014186-99014202 chr4:99014192-99014199
47	CTCF	chr4:99014120-99014270	GM12878	blood:	n/a	chr4:99014180-99014201 chr4:99014185-99014203 chr4:99014186-99014202 chr4:99014192-99014199
48	CTCF	chr4:98905760-98905910	HEEpiC	esophagus:	n/a	n/a
49	CTCF	chr4:99014119-99014238	MCF-7	breast:	n/a	chr4:99014180-99014201 chr4:99014185-99014203 chr4:99014186-99014202 chr4:99014192-99014199
50	CTCF	chr4:98908323-98908418	Lung_OC	lung:	n/a	chr4:98908367-98908388 chr4:98908372-98908390

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:99008595-99008645	ECC-1	luminal epithelium:	n/a
2	chr4:99008595-99008645	ECC-1	luminal epithelium:	n/a
3	chr4:99031533-99031583	SK-N-SH_RA	brain:	n/a
4	chr4:99008595-99008645	H1-hESC	embryonic stem cell:	embryo
5	chr4:99008595-99008645	NHBE	bronchial:	n/a
6	chr4:99031533-99031583	HPAEpiC	pulmonary alveolar:	n/a
7	chr4:99008595-99008645	BJ	skin:	n/a
8	chr4:99008595-99008645	IMR90	lung:	fetal
9	chr4:99031533-99031583	LNCaP	prostate:	n/a
10	chr4:99031533-99031583	HRE	kidney:	n/a
11	chr4:99031533-99031583	GM06990	blood:	n/a
12	chr4:99008595-99008645	HRE	kidney:	n/a
13	chr4:99031533-99031583	AG10803	skin:	n/a
14	chr4:99008595-99008645	A549	lung:	n/a
15	chr4:99031533-99031583	MCF10A-Er-Src	breast:	n/a
16	chr4:99008595-99008645	SKMC	muscle:	n/a
17	chr4:99008595-99008645	AG10803	skin:	n/a
18	chr4:99008595-99008645	Caco-2	colon:	n/a
19	chr4:99008595-99008645	NB4	blood:	n/a
20	chr4:99031533-99031583	PANC-1	pancreas:	n/a
21	chr4:99031533-99031583	GM19239	blood:	n/a
22	chr4:99031533-99031583	CMK	blood:	n/a
23	chr4:99031533-99031583	T-47D	breast:	n/a
24	chr4:99031533-99031583	HEK293	kidney:	embryo
25	chr4:99031533-99031583	BJ	skin:	n/a
26	chr4:99031533-99031583	HepG2	liver:	n/a
27	chr4:99008595-99008645	HCM	heart:	n/a
28	chr4:99031533-99031583	HRPEpiC	eye:	n/a
29	chr4:99031533-99031583	GM12878	blood:	n/a
30	chr4:99031533-99031583	HAEpiC	amniotic membrane:	n/a
31	chr4:99031533-99031583	AG09319	gingival:	n/a
32	chr4:99008595-99008645	GM12891	blood:	n/a
33	chr4:99008595-99008645	K562	blood:	n/a
34	chr4:99008595-99008645	AG04449	skin:	fetal
35	chr4:99008595-99008645	PrEC	prostate:	n/a
36	chr4:99008595-99008645	AG09319	gingival:	n/a
37	chr4:99031533-99031583	PrEC	prostate:	n/a
38	chr4:99008595-99008645	HEK293	kidney:	embryo
39	chr4:99008595-99008645	SK-N-MC	brain:	n/a
40	chr4:99031533-99031583	SKMC	muscle:	n/a
41	chr4:99031533-99031583	H1-hESC	embryonic stem cell:	embryo
42	chr4:99031533-99031583	GM12892	blood:	n/a
43	chr4:99031533-99031583	Caco-2	colon:	n/a
44	chr4:99008595-99008645	SAEC	small airway:	n/a
45	chr4:99008595-99008645	MCF10A-Er-Src	breast:	n/a
46	chr4:99008595-99008645	SK-N-SH_RA	brain:	n/a
47	chr4:99031533-99031583	K562	blood:	n/a
48	chr4:99008595-99008645	T-47D	breast:	n/a
49	chr4:99031533-99031583	NHBE	bronchial:	n/a
50	chr4:99031533-99031583	SK-N-SH	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:97404242..97405044-chr4:98905771..98906367,3	MCF-7	breast:
2	chr4:99002780..99005606-chr4:99010089..99012416,2	MCF-7	breast:
3	chr4:98790810..98793729-chr4:98795373..98798047,2	K562	blood:
4	chr4:98641928..98642827-chr4:98905748..98906362,2	MCF-7	breast:
5	chr4:98896668..98898608-chr4:98901811..98903490,2	K562	blood:
6	chr4:98967509..98968412-chr4:99013843..99014513,4	MCF-7	breast:
7	chr4:99001766..99003673-chr4:99063340..99066059,2	MCF-7	breast:
8	chr4:99012356..99014792-chr4:99062792..99064417,2	MCF-7	breast:
9	chr4:98995356..98997429-chr4:98998775..99000432,2	MCF-7	breast:
10	chr4:98765331..98767165-chr4:99012892..99015543,2	K562	blood:
11	chr4:98967509..98968412-chr4:99013843..99014513,4	MCF-7	breast:
12	chr4:99002780..99005606-chr4:99010089..99012416,2	MCF-7	breast:
13	chr4:98790810..98793729-chr4:98795373..98798047,2	K562	blood:
14	chr4:98896668..98898608-chr4:98901811..98903490,2	K562	blood:
15	chr4:98995356..98997429-chr4:98998775..99000432,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RAP1GDS1-6	chr4:98969706-98970194	NONHSAT097481
2	lnc-TSPAN5-3	chr4:98814203-98814354	NONHSAT097477

Variant related genes	Relation type
STPG2	TF binding region
RPL5P12	TF binding region
CRYZP2	TF binding region
DUTP8	TF binding region
STPG2	CpG island
RPL5P12	CpG island
CRYZP2	CpG island
DUTP8	CpG island
ENSG00000163116	chromatin interactions

Extended variants
information (count: 3343 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:3343 , 50 per page) page: 1 2 3 4 5 6 7 ... 67

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs72686434	chr4:98787209-98787210	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs541386854	chr4:98787224-98787225	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs574417631	chr4:98787258-98787259	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs190802560	chr4:98787280-98787281	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs560466591	chr4:98787323-98787324	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs113263378	chr4:98787329-98787330	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs527556213	chr4:98787343-98787344	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs34159897	chr4:98787367-98787368	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs564340806	chr4:98787382-98787383	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs183998175	chr4:98787395-98787396	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs550288348	chr4:98787425-98787426	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs67274661	chr4:98787432-98787433	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs535843940	chr4:98787433-98787434	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs559490229	chr4:98787434-98787435	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs145708282	chr4:98787483-98787484	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs151109829	chr4:98787534-98787535	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs369498537	chr4:98787580-98787581	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs558005344	chr4:98787606-98787607	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs140953881	chr4:98787623-98787624	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs79095080	chr4:98787666-98787667	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs556237061	chr4:98787673-98787674	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs574404995	chr4:98787675-98787676	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs11464717	chr4:98787680-98787681	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs397691825	chr4:98787687-98787688	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs571035198	chr4:98787695-98787696	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs552022770	chr4:98787744-98787745	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs560601276	chr4:98787791-98787792	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs77528183	chr4:98787818-98787819	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs546500122	chr4:98787819-98787820	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs546165752	chr4:98787838-98787839	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs117793346	chr4:98787881-98787882	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs145693569	chr4:98787909-98787910	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs549661959	chr4:98788010-98788011	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs562231068	chr4:98788011-98788012	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs529311405	chr4:98788055-98788056	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs138050815	chr4:98788061-98788062	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs561885168	chr4:98788068-98788069	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs200717575	chr4:98788070-98788071	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs547468523	chr4:98788071-98788072	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs565762346	chr4:98788079-98788080	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs549154999	chr4:98788088-98788089	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs374194738	chr4:98788154-98788155	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs551700002	chr4:98788183-98788184	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs193276682	chr4:98788194-98788195	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs537657273	chr4:98788216-98788217	Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs555654081	chr4:98788223-98788224	Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs574491507	chr4:98788232-98788233	Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs535580467	chr4:98788253-98788254	Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs553882893	chr4:98788257-98788258	Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs572111014	chr4:98788295-98788296	Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:83)

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
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
Myelodysplastic syndrome	21251322	CNVD
Lung cancer	18438408	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	18414403	CNVD
primary effusion lymphomas	17116491	CNVD
small cell lung cancer	20016488	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17133270	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Colorectal cancer	20459617	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Hirschsprung''s Disease	21712996	CNVD
Congenital anomalies of the kidney and urinary tract	20505237	CNVD
Breast cancer	17393978	CNVD
Ovarian cancer	21720365	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Esophageal cancer	21851588	CNVD
Cancer	19907438	CNVD
Prostate cancer	16573809	CNVD
Multiple myeloma	16616336	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	19197363	CNVD
Melanoma	20688739	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD
Schizophrenia	23813976	CNVD
Gastric cancer	16891809	CNVD
Bipolar disorder	19114987	CNVD

Chromatin state (count:154 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:98787200-98787400	Enhancers	Fetal Kidney	kidney
2	chr4:98787200-98788200	Enhancers	Liver	Liver
3	chr4:98787400-98788800	Weak transcription	Fetal Kidney	kidney
4	chr4:98788000-98788200	Enhancers	Pancreas	Pancrea
5	chr4:98788200-98789400	Flanking Active TSS	Liver	Liver
6	chr4:98788400-98789000	Enhancers	Pancreatic Islets	Pancreatic Islet
7	chr4:98788400-98789400	Enhancers	Brain Germinal Matrix	brain
8	chr4:98788400-98789600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr4:98788400-98789800	Enhancers	Fetal Lung	lung
10	chr4:98788800-98789000	Enhancers	Pancreas	Pancrea
11	chr4:98788800-98789200	Enhancers	HUVEC	blood vessel
12	chr4:98788800-98790000	Enhancers	Fetal Kidney	kidney
13	chr4:98789400-98791200	Enhancers	Liver	Liver
14	chr4:98794000-98794200	Enhancers	iPS-18 Cell Line	embryonic stem cell
15	chr4:98794200-98795200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
16	chr4:98795200-98795600	Enhancers	iPS-18 Cell Line	embryonic stem cell
17	chr4:98795400-98795800	Enhancers	iPS-20b Cell Line	embryonic stem cell
18	chr4:98797000-98797600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
19	chr4:98813600-98814000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
20	chr4:98813600-98814000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr4:98820800-98821200	Enhancers	H1 Cell Line	embryonic stem cell
22	chr4:98821000-98821400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
23	chr4:98821000-98822000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
24	chr4:98821200-98821600	Weak transcription	H1 Cell Line	embryonic stem cell
25	chr4:98821200-98822000	Enhancers	HUES48 Cell Line	embryonic stem cell
26	chr4:98821400-98821800	Enhancers	iPS-20b Cell Line	embryonic stem cell
27	chr4:98821600-98821800	Enhancers	H1 Cell Line	embryonic stem cell
28	chr4:98821600-98821800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
29	chr4:98821600-98822000	Enhancers	iPS-18 Cell Line	embryonic stem cell
30	chr4:98821800-98824800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
31	chr4:98821800-98832400	Weak transcription	H1 Cell Line	embryonic stem cell
32	chr4:98822000-98824600	Weak transcription	HUES48 Cell Line	embryonic stem cell
33	chr4:98822000-98824800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
34	chr4:98824200-98824600	Enhancers	ES-I3 Cell Line	embryonic stem cell
35	chr4:98824400-98824800	Enhancers	HUES64 Cell Line	embryonic stem cell
36	chr4:98824600-98825200	Active TSS	ES-I3 Cell Line	embryonic stem cell
37	chr4:98824600-98825200	Active TSS	ES-WA7 Cell Line	embryonic stem cell
38	chr4:98824600-98825200	Active TSS	HUES48 Cell Line	embryonic stem cell
39	chr4:98824600-98825200	Active TSS	HUES6 Cell Line	embryonic stem cell
40	chr4:98824800-98825000	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
41	chr4:98824800-98825000	Enhancers	iPS-20b Cell Line	embryonic stem cell
42	chr4:98824800-98825200	Active TSS	H9 Cell Line	embryonic stem cell
43	chr4:98824800-98825200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr4:98824800-98825200	Active TSS	iPS-15b Cell Line	embryonic stem cell
45	chr4:98824800-98825200	Active TSS	iPS-18 Cell Line	embryonic stem cell
46	chr4:98825000-98825200	Active TSS	HUES64 Cell Line	embryonic stem cell
47	chr4:98825200-98825400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
48	chr4:98825200-98825600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
49	chr4:98825400-98825800	Enhancers	iPS-18 Cell Line	embryonic stem cell
50	chr4:98825600-98825800	Enhancers	iPS-15b Cell Line	embryonic stem cell

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