Variant report

Variant	nsv1003350
Chromosome Location	chr4:93566813-93821353
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	BACH1	chr4:93728575-93728662	K562	blood:	n/a	n/a
2	BATF	chr4:93668507-93668738	GM12878	blood:	n/a	n/a
3	CEBPB	chr4:93655856-93656165	IMR90	lung:	n/a	chr4:93655985-93655996
4	CEBPB	chr4:93744766-93744818	K562	blood:	n/a	chr4:93744785-93744794 chr4:93744785-93744794 chr4:93744785-93744794 chr4:93744785-93744796 chr4:93744785-93744794 chr4:93744783-93744796
5	CEBPB	chr4:93730580-93730850	K562	blood:	n/a	chr4:93730724-93730735 chr4:93730738-93730749
6	CEBPB	chr4:93594339-93594550	HepG2	liver:	n/a	chr4:93594475-93594486
7	CEBPB	chr4:93730571-93730930	Hela-S3	cervix:	n/a	chr4:93730724-93730735 chr4:93730738-93730749
8	CEBPB	chr4:93730570-93730923	HepG2	liver:	n/a	chr4:93730724-93730735 chr4:93730738-93730749
9	CEBPB	chr4:93796324-93796523	HepG2	liver:	n/a	chr4:93796369-93796380
10	CEBPB	chr4:93655859-93656159	H1-hESC	embryonic stem cell:	n/a	chr4:93655985-93655996
11	CEBPB	chr4:93689167-93689298	H1-hESC	embryonic stem cell:	n/a	chr4:93689218-93689229
12	CEBPB	chr4:93684639-93684709	A549	lung:	n/a	chr4:93684658-93684669
13	CEBPB	chr4:93569424-93569686	HepG2	liver:	n/a	chr4:93569576-93569587
14	CEBPB	chr4:93646297-93646482	IMR90	lung:	n/a	n/a
15	CEBPB	chr4:93638461-93638652	A549	lung:	n/a	chr4:93638520-93638531
16	CEBPB	chr4:93655912-93656149	MCF-7	breast:	n/a	chr4:93655985-93655996
17	CEBPB	chr4:93681954-93682242	HepG2	liver:	n/a	chr4:93682086-93682097
18	CEBPB	chr4:93730554-93730928	IMR90	lung:	n/a	chr4:93730724-93730735 chr4:93730738-93730749
19	CEBPB	chr4:93730562-93730917	H1-hESC	embryonic stem cell:	n/a	chr4:93730724-93730735 chr4:93730738-93730749
20	CEBPB	chr4:93644439-93644669	HepG2	liver:	n/a	chr4:93644563-93644574 chr4:93644563-93644576
21	CEBPB	chr4:93730558-93730864	MCF-7	breast:	n/a	chr4:93730724-93730735 chr4:93730738-93730749
22	CEBPB	chr4:93795845-93796108	HepG2	liver:	n/a	chr4:93795963-93795974
23	CEBPB	chr4:93730571-93730943	ECC-1	luminal epithelium:	n/a	chr4:93730724-93730735 chr4:93730738-93730749
24	CEBPB	chr4:93592781-93592941	H1-hESC	embryonic stem cell:	n/a	n/a
25	CEBPB	chr4:93638386-93638647	HepG2	liver:	n/a	chr4:93638520-93638531
26	CEBPB	chr4:93594437-93594615	K562	blood:	n/a	chr4:93594475-93594486
27	CEBPB	chr4:93689119-93689335	K562	blood:	n/a	chr4:93689218-93689229
28	CEBPB	chr4:93655882-93656153	HepG2	liver:	n/a	chr4:93655985-93655996
29	CEBPB	chr4:93591113-93591283	K562	blood:	n/a	chr4:93591137-93591150
30	CEBPB	chr4:93646285-93646553	H1-hESC	embryonic stem cell:	n/a	n/a
31	CEBPB	chr4:93684631-93684724	HepG2	liver:	n/a	chr4:93684658-93684669
32	CEBPB	chr4:93681975-93682265	A549	lung:	n/a	chr4:93682086-93682097
33	CEBPB	chr4:93796260-93796522	H1-hESC	embryonic stem cell:	n/a	chr4:93796369-93796380
34	CEBPB	chr4:93655972-93656033	K562	blood:	n/a	chr4:93655985-93655996
35	CEBPB	chr4:93730582-93730952	MCF-7	breast:	n/a	chr4:93730724-93730735 chr4:93730738-93730749
36	CEBPB	chr4:93730575-93730933	A549	lung:	n/a	chr4:93730724-93730735 chr4:93730738-93730749
37	CEBPB	chr4:93753510-93753717	H1-hESC	embryonic stem cell:	n/a	n/a
38	CEBPB	chr4:93795868-93796039	IMR90	lung:	n/a	chr4:93795963-93795974
39	CEBPB	chr4:93730552-93730878	ECC-1	luminal epithelium:	n/a	chr4:93730724-93730735 chr4:93730738-93730749
40	CEBPB	chr4:93806171-93806461	HepG2	liver:	n/a	n/a
41	CEBPB	chr4:93582745-93582936	HepG2	liver:	n/a	chr4:93582923-93582932 chr4:93582923-93582934
42	CTCF	chr4:93807280-93807430	MCF-7	breast:	n/a	n/a
43	CTCF	chr4:93781000-93781150	GM12873	blood:	n/a	n/a
44	CTCF	chr4:93805041-93805254	GM12878	blood:	n/a	n/a
45	CTCF	chr4:93746868-93746973	GM20000	blood:	n/a	n/a
46	CTCF	chr4:93656343-93656407	Medullo	brain:	n/a	n/a
47	CTCF	chr4:93598780-93598930	AG10803	skin:	n/a	n/a
48	CTCF	chr4:93632908-93632972	LNCaP	prostate:	n/a	n/a
49	CTCF	chr4:93780940-93781090	WERI-Rb-1	eye:	n/a	n/a
50	CTCF	chr4:93656310-93656609	MCF-7	breast:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:93646144-93646194	AoSMC	blood vessel:	n/a
2	chr4:93646144-93646194	H1-hESC	embryonic stem cell:	embryo
3	chr4:93646144-93646194	HEK293	kidney:	embryo
4	chr4:93646144-93646194	NB4	blood:	n/a
5	chr4:93646144-93646194	T-47D	breast:	n/a
6	chr4:93646144-93646194	HUVEC	blood vessel:	n/a
7	chr4:93646144-93646194	CMK	blood:	n/a
8	chr4:93646144-93646194	LNCaP	prostate:	n/a
9	chr4:93646144-93646194	NHDF-neo	bronchial:	n/a
10	chr4:93646144-93646194	HCM	heart:	n/a
11	chr4:93646144-93646194	AG09309	skin:	n/a
12	chr4:93646144-93646194	GM12891	blood:	n/a
13	chr4:93646144-93646194	SAEC	small airway:	n/a
14	chr4:93646144-93646194	PrEC	prostate:	n/a
15	chr4:93646144-93646194	ProgFib	skin:	n/a
16	chr4:93646144-93646194	GM12892	blood:	n/a
17	chr4:93646144-93646194	A549	lung:	n/a
18	chr4:93646144-93646194	SK-N-MC	brain:	n/a
19	chr4:93646144-93646194	SK-N-SH_RA	brain:	n/a
20	chr4:93646144-93646194	Jurkat	blood:	n/a
21	chr4:93646144-93646194	HRPEpiC	eye:	n/a
22	chr4:93646144-93646194	NHBE	bronchial:	n/a
23	chr4:93646144-93646194	NT2-D1	testis:	n/a
24	chr4:93646144-93646194	HNPCEpiC	eye:	n/a
25	chr4:93646144-93646194	HMEC	breast:	n/a
26	chr4:93646144-93646194	SKMC	muscle:	n/a
27	chr4:93646144-93646194	ovcar-3	ovarian:	n/a
28	chr4:93646144-93646194	HRCEpiC	kidney:	n/a
29	chr4:93646144-93646194	GM12878	blood:	n/a
30	chr4:93646144-93646194	K562	blood:	n/a
31	chr4:93646144-93646194	Caco-2	colon:	n/a
32	chr4:93646144-93646194	SK-N-SH	brain:	n/a
33	chr4:93646144-93646194	HPAEpiC	pulmonary alveolar:	n/a
34	chr4:93646144-93646194	HCF	heart:	n/a
35	chr4:93646144-93646194	ECC-1	luminal epithelium:	n/a
36	chr4:93646144-93646194	U87	brain:	n/a
37	chr4:93646144-93646194	HL-60	blood:	n/a
38	chr4:93646144-93646194	HCT-116	colon:	n/a
39	chr4:93646144-93646194	HAEpiC	amniotic membrane:	n/a
40	chr4:93646144-93646194	BE2_C	brain:	n/a
41	chr4:93646144-93646194	NH-A	brain:	n/a
42	chr4:93646144-93646194	HCPEpiC	choroid plexus:	n/a
43	chr4:93646144-93646194	AG04450	lung:	fetal
44	chr4:93646144-93646194	MCF10A-Er-Src	breast:	n/a
45	chr4:93646144-93646194	PANC-1	pancreas:	n/a
46	chr4:93646144-93646194	AG04449	skin:	fetal
47	chr4:93646144-93646194	GM19239	blood:	n/a
48	chr4:93646144-93646194	GM06990	blood:	n/a
49	chr4:93646144-93646194	PFSK-1	brain:	n/a
50	chr4:93646144-93646194	AG10803	skin:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:93757984..93759775-chr4:93817140..93819795,2	MCF-7	breast:
2	chr4:93577929..93580454-chr4:93584774..93587320,2	K562	blood:
3	chr4:93640334..93641891-chr4:93646345..93648572,2	MCF-7	breast:
4	chr4:93679723..93682037-chr4:93683419..93685148,2	K562	blood:
5	chr4:93679723..93682037-chr4:93683419..93685148,2	K562	blood:
6	chr4:93679131..93681725-chr4:93686462..93688437,2	K562	blood:
7	chr4:93773449..93776266-chr4:93779103..93780772,2	MCF-7	breast:
8	chr4:93773449..93776266-chr4:93779103..93780772,2	MCF-7	breast:
9	chr4:93757984..93759775-chr4:93817140..93819795,2	MCF-7	breast:
10	chr4:93640334..93641891-chr4:93646345..93648572,2	MCF-7	breast:
11	chr4:93667707..93669873-chr4:93672761..93675696,2	K562	blood:
12	chr4:93679131..93681725-chr4:93686462..93688437,2	K562	blood:
13	chr4:93667707..93669873-chr4:93672761..93675696,2	K562	blood:
14	chr4:93577929..93580454-chr4:93584774..93587320,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-9B6.1.1-2	chr4:93759934-93759993	ENSG00000248627.1
2	lnc-ATOH1-1	chr4:93805814-93806258	NONHSAT097436
3	lnc-RP11-9B6.1.1-2	chr4:93754836-93755124	ENSG00000248627.1
4	lnc-RP11-9B6.1.1-6	chr4:93743137-93744069	NONHSAT097434

Variant related genes	Relation type
ENSG00000248750	TF binding region
MTND1P19	TF binding region
GRID2	TF binding region
ENSG00000249239	TF binding region
ENSG00000248627	TF binding region
ENSG00000248750	CpG island
MTND1P19	CpG island
GRID2	CpG island
ENSG00000249239	CpG island
ENSG00000248627	CpG island

Extended variants
information (count: 9521 )
Associated
traits (count: 94 )

Variant overlapped rSNPs/rCNVs (count:9521 , 50 per page) page: 1 2 3 4 5 6 7 ... 191

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs572438664	chr4:93566819-93566820	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs182034321	chr4:93566840-93566841	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs541561632	chr4:93566856-93566857	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs531170888	chr4:93566860-93566861	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs549590417	chr4:93566924-93566925	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs571417870	chr4:93566966-93566967	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs62309177	chr4:93566973-93566974	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs185134479	chr4:93566989-93566990	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs138312076	chr4:93567005-93567006	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs547368300	chr4:93567006-93567007	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs367687339	chr4:93567010-93567011	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs190278619	chr4:93567062-93567063	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs181102793	chr4:93567075-93567076	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs565697992	chr4:93567103-93567104	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs571464049	chr4:93567127-93567128	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs370984826	chr4:93567134-93567135	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs527372268	chr4:93567151-93567152	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs547501773	chr4:93567177-93567178	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs150178582	chr4:93567210-93567211	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs536227947	chr4:93567272-93567273	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs62309178	chr4:93567311-93567312	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs549808194	chr4:93567314-93567315	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs371446702	chr4:93567355-93567356	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs375814634	chr4:93567356-93567357	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs370177573	chr4:93567357-93567358	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs570326052	chr4:93567382-93567383	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs186660199	chr4:93567424-93567425	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs536120705	chr4:93567427-93567428	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs199624859	chr4:93567434-93567435	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs558880901	chr4:93567448-93567449	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs572629342	chr4:93567481-93567482	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs138647400	chr4:93567496-93567497	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs555018777	chr4:93567543-93567544	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs574594918	chr4:93567587-93567588	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs543370919	chr4:93567590-93567591	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs563383486	chr4:93567596-93567597	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs56077205	chr4:93567627-93567628	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs79559978	chr4:93567631-93567632	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs369965016	chr4:93567707-93567708	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs545312644	chr4:93567731-93567732	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs554879749	chr4:93567756-93567757	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs564914375	chr4:93567768-93567769	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs572208412	chr4:93567770-93567771	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs527445857	chr4:93567772-93567773	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs190657865	chr4:93567783-93567784	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs532168119	chr4:93567846-93567847	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs560994111	chr4:93567887-93567888	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs376993559	chr4:93567904-93567905	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs529825903	chr4:93567919-93567920	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs549796189	chr4:93567934-93567935	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:94)

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
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
Hodgkin''s lymphoma	17606441	CNVD
Esophageal cancer	21851588	CNVD
Cancer	19907438	CNVD
early-passage human iPS cells	21368824	CNVD
Breast cancer	22522925	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Bipolar disorder	19114987	CNVD
Autism	20841430	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Cancer	20164919	CNVD
Prostate cancer	16573809	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Glioma	20126413	CNVD

Chromatin state (count:232 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:93550000-93574800	Weak transcription	H1 Cell Line	embryonic stem cell
2	chr4:93552000-93579000	Weak transcription	HUES64 Cell Line	embryonic stem cell
3	chr4:93554400-93570400	Weak transcription	HUES48 Cell Line	embryonic stem cell
4	chr4:93568000-93568400	Enhancers	Brain Substantia Nigra	brain
5	chr4:93569400-93575200	Weak transcription	H9 Cell Line	embryonic stem cell
6	chr4:93570400-93571200	Strong transcription	HUES48 Cell Line	embryonic stem cell
7	chr4:93571200-93577800	Weak transcription	HUES48 Cell Line	embryonic stem cell
8	chr4:93574800-93575000	Enhancers	H1 Cell Line	embryonic stem cell
9	chr4:93575200-93575400	Enhancers	H9 Cell Line	embryonic stem cell
10	chr4:93577800-93579800	Enhancers	HUES48 Cell Line	embryonic stem cell
11	chr4:93579000-93579600	Enhancers	HUES64 Cell Line	embryonic stem cell
12	chr4:93579600-93580600	Weak transcription	HUES64 Cell Line	embryonic stem cell
13	chr4:93579800-93590600	Weak transcription	HUES48 Cell Line	embryonic stem cell
14	chr4:93580600-93580800	Enhancers	HUES64 Cell Line	embryonic stem cell
15	chr4:93587600-93587800	Enhancers	HUES6 Cell Line	embryonic stem cell
16	chr4:93587800-93591800	Weak transcription	HUES6 Cell Line	embryonic stem cell
17	chr4:93590400-93590800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr4:93590600-93591400	Enhancers	iPS-15b Cell Line	embryonic stem cell
19	chr4:93590600-93592000	Enhancers	ES-I3 Cell Line	embryonic stem cell
20	chr4:93590600-93592000	Enhancers	HUES48 Cell Line	embryonic stem cell
21	chr4:93591400-93592000	Enhancers	HUES64 Cell Line	embryonic stem cell
22	chr4:93591400-93592400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
23	chr4:93591400-93592400	Enhancers	iPS-18 Cell Line	embryonic stem cell
24	chr4:93591800-93592600	Enhancers	HUES6 Cell Line	embryonic stem cell
25	chr4:93592000-93595200	Weak transcription	HUES48 Cell Line	embryonic stem cell
26	chr4:93592400-93592600	Enhancers	iPS-15b Cell Line	embryonic stem cell
27	chr4:93595200-93595600	Strong transcription	HUES48 Cell Line	embryonic stem cell
28	chr4:93595600-93598600	Weak transcription	HUES48 Cell Line	embryonic stem cell
29	chr4:93598200-93599200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
30	chr4:93598600-93599200	Enhancers	HUES48 Cell Line	embryonic stem cell
31	chr4:93599200-93624000	Weak transcription	HUES48 Cell Line	embryonic stem cell
32	chr4:93601600-93602000	Enhancers	Brain Angular Gyrus	brain
33	chr4:93606400-93612600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
34	chr4:93606400-93617200	Weak transcription	HUES64 Cell Line	embryonic stem cell
35	chr4:93607600-93612200	Weak transcription	H1 Cell Line	embryonic stem cell
36	chr4:93618200-93618800	Enhancers	Fetal Intestine Large	intestine
37	chr4:93622800-93623200	Enhancers	Liver	Liver
38	chr4:93623000-93623800	Enhancers	Fetal Intestine Small	intestine
39	chr4:93629200-93631600	Weak transcription	H1 Cell Line	embryonic stem cell
40	chr4:93630200-93635000	Weak transcription	HUES6 Cell Line	embryonic stem cell
41	chr4:93630200-93655400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
42	chr4:93630600-93635800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
43	chr4:93631600-93633000	Strong transcription	H1 Cell Line	embryonic stem cell
44	chr4:93633000-93646000	Weak transcription	H1 Cell Line	embryonic stem cell
45	chr4:93635000-93636000	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
46	chr4:93635800-93636000	Enhancers	H9 Cell Line	embryonic stem cell
47	chr4:93635800-93636000	Enhancers	HUES48 Cell Line	embryonic stem cell
48	chr4:93635800-93636400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
49	chr4:93636000-93653600	Weak transcription	HUES6 Cell Line	embryonic stem cell
50	chr4:93636000-93687200	Weak transcription	HUES48 Cell Line	embryonic stem cell

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