Variant report

Variant	nsv879599
Chromosome Location	chr4:92906792-93062161
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	BATF	chr4:92956941-92957201	GM12878	blood:	n/a	chr4:92957060-92957071
2	BATF	chr4:92956979-92957141	GM12878	blood:	n/a	chr4:92957060-92957071
3	BHLHE40	chr4:92956890-92957081	GM12878	blood:	n/a	n/a
4	BRCA1	chr4:93023011-93023329	Hela-S3	cervix:	n/a	n/a
5	CEBPB	chr4:92935220-92935612	ECC-1	luminal epithelium:	n/a	chr4:92935406-92935415 chr4:92935406-92935417 chr4:92935406-92935415 chr4:92935404-92935415 chr4:92935406-92935415 chr4:92935404-92935417 chr4:92935404-92935417 chr4:92935406-92935415
6	CEBPB	chr4:92935217-92935603	K562	blood:	n/a	chr4:92935406-92935415 chr4:92935406-92935417 chr4:92935406-92935415 chr4:92935404-92935415 chr4:92935406-92935415 chr4:92935404-92935417 chr4:92935404-92935417 chr4:92935406-92935415
7	CEBPB	chr4:92996956-92997134	HepG2	liver:	n/a	chr4:92997092-92997103 chr4:92997070-92997081 chr4:92997091-92997102 chr4:92997091-92997104
8	CEBPB	chr4:92935277-92935519	HepG2	liver:	n/a	chr4:92935406-92935415 chr4:92935406-92935417 chr4:92935406-92935415 chr4:92935404-92935415 chr4:92935406-92935415 chr4:92935404-92935417 chr4:92935404-92935417 chr4:92935406-92935415
9	CEBPB	chr4:92935231-92935597	H1-hESC	embryonic stem cell:	n/a	chr4:92935406-92935415 chr4:92935406-92935417 chr4:92935406-92935415 chr4:92935404-92935415 chr4:92935406-92935415 chr4:92935404-92935417 chr4:92935404-92935417 chr4:92935406-92935415
10	CEBPB	chr4:92932360-92932620	HepG2	liver:	n/a	chr4:92932505-92932516
11	CEBPB	chr4:92935286-92935564	HepG2	liver:	n/a	chr4:92935406-92935415 chr4:92935406-92935417 chr4:92935406-92935415 chr4:92935404-92935415 chr4:92935406-92935415 chr4:92935404-92935417 chr4:92935404-92935417 chr4:92935406-92935415
12	CEBPB	chr4:92935244-92935570	Hela-S3	cervix:	n/a	chr4:92935406-92935415 chr4:92935406-92935417 chr4:92935406-92935415 chr4:92935404-92935415 chr4:92935406-92935415 chr4:92935404-92935417 chr4:92935404-92935417 chr4:92935406-92935415
13	CEBPB	chr4:92935223-92935591	A549	lung:	n/a	chr4:92935406-92935415 chr4:92935406-92935417 chr4:92935406-92935415 chr4:92935404-92935415 chr4:92935406-92935415 chr4:92935404-92935417 chr4:92935404-92935417 chr4:92935406-92935415
14	CEBPB	chr4:92926988-92927324	HepG2	liver:	n/a	chr4:92927164-92927177 chr4:92927166-92927175 chr4:92927166-92927177 chr4:92927164-92927175
15	CEBPB	chr4:92935255-92935558	MCF-7	breast:	n/a	chr4:92935406-92935415 chr4:92935406-92935417 chr4:92935406-92935415 chr4:92935404-92935415 chr4:92935406-92935415 chr4:92935404-92935417 chr4:92935404-92935417 chr4:92935406-92935415
16	CEBPB	chr4:93018727-93018912	HepG2	liver:	n/a	chr4:93018797-93018808 chr4:93018795-93018806
17	CEBPB	chr4:92935216-92935599	IMR90	lung:	n/a	chr4:92935406-92935415 chr4:92935406-92935417 chr4:92935406-92935415 chr4:92935404-92935415 chr4:92935406-92935415 chr4:92935404-92935417 chr4:92935404-92935417 chr4:92935406-92935415
18	CEBPB	chr4:92935210-92935609	HepG2	liver:	n/a	chr4:92935406-92935415 chr4:92935406-92935417 chr4:92935406-92935415 chr4:92935404-92935415 chr4:92935406-92935415 chr4:92935404-92935417 chr4:92935404-92935417 chr4:92935406-92935415
19	CEBPB	chr4:93022762-93023420	Hela-S3	cervix:	n/a	chr4:93023015-93023028 chr4:93022982-93022993 chr4:93023015-93023026 chr4:93023016-93023027 chr4:93022983-93022994
20	CEBPB	chr4:92932501-92932580	Hela-S3	cervix:	n/a	chr4:92932505-92932516
21	CEBPB	chr4:92932347-92932681	IMR90	lung:	n/a	chr4:92932505-92932516
22	CEBPB	chr4:92935234-92935591	HepG2	liver:	n/a	chr4:92935406-92935415 chr4:92935406-92935417 chr4:92935406-92935415 chr4:92935404-92935415 chr4:92935406-92935415 chr4:92935404-92935417 chr4:92935404-92935417 chr4:92935406-92935415
23	CEBPB	chr4:93022790-93023139	HepG2	liver:	n/a	chr4:93023015-93023028 chr4:93022982-93022993 chr4:93023015-93023026 chr4:93023016-93023027 chr4:93022983-93022994
24	CEBPB	chr4:93022867-93023188	A549	lung:	n/a	chr4:93023015-93023028 chr4:93022982-93022993 chr4:93023015-93023026 chr4:93023016-93023027 chr4:93022983-93022994
25	CEBPB	chr4:92932419-92932555	K562	blood:	n/a	chr4:92932505-92932516
26	CREB1	chr4:92956973-92957308	GM12878	blood:	n/a	n/a
27	CTCF	chr4:92911200-92911350	HMEC	breast:	n/a	n/a
28	CTCF	chr4:93012680-93012830	GM12866	blood:	n/a	n/a
29	CTCF	chr4:93012700-93012850	HCM	heart:	n/a	n/a
30	CTCF	chr4:92968709-92969028	GM12878	blood:	n/a	n/a
31	CTCF	chr4:93012605-93012738	SK-N-SH_RA	brain:	n/a	n/a
32	CTCF	chr4:93012620-93012770	GM12868	blood:	n/a	n/a
33	CTCF	chr4:92911260-92911410	GM12874	blood:	n/a	n/a
34	CTCF	chr4:92934920-92935070	HCM	heart:	n/a	n/a
35	CTCF	chr4:92934720-92934870	GM12872	blood:	n/a	n/a
36	CTCF	chr4:92968626-92969112	MCF-7	breast:	n/a	n/a
37	CTCF	chr4:92981640-92981790	GM12873	blood:	n/a	n/a
38	CTCF	chr4:92959669-92959688	Lung_OC	lung:	n/a	n/a
39	CTCF	chr4:92934720-92934870	A549	lung:	n/a	n/a
40	CTCF	chr4:93012580-93012730	HAc	cerebellar:	n/a	n/a
41	CTCF	chr4:92934660-92934810	HEK293	kidney:	n/a	n/a
42	CTCF	chr4:92934700-92934850	HMF	breast:	n/a	n/a
43	CTCF	chr4:93012560-93012772	MCF-7	breast:	n/a	n/a
44	CTCF	chr4:93012600-93012750	HBMEC	blood vessel:	n/a	n/a
45	CTCF	chr4:92934800-92935010	HEEpiC	esophagus:	n/a	n/a
46	CTCF	chr4:93012680-93012830	HCT-116	colon:	n/a	n/a
47	CTCF	chr4:92934742-92934912	Lung_OC	lung:	n/a	n/a
48	CTCF	chr4:92934660-92934810	HA-sp	spinal cord:	n/a	n/a
49	CTCF	chr4:93012600-93012750	GM12878	blood:	n/a	n/a
50	CTCF	chr4:93012460-93012610	HCM	heart:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:93041952..93042462-chr4:93063543..93064136,2	MCF-7	breast:
2	chr4:93044602..93046787-chr4:93048127..93050943,2	MCF-7	breast:
3	chr4:93027385..93029729-chr4:93033798..93036678,2	K562	blood:
4	chr1:150602085..150602904-chr4:92944319..92945074,2	NB4	blood:
5	chr4:93022151..93024082-chr4:93025859..93028241,2	MCF-7	breast:
6	chr4:93022151..93024082-chr4:93025859..93028241,2	MCF-7	breast:
7	chr4:93044602..93046787-chr4:93048127..93050943,2	MCF-7	breast:
8	chr4:93041952..93042761-chr4:93063494..93064136,3	MCF-7	breast:
9	chr17:56736322..56736880-chr4:92908655..92909344,2	MCF-7	breast:
10	chr4:93036522..93038692-chr4:93040395..93042762,2	MCF-7	breast:
11	chr4:93027385..93029729-chr4:93033798..93036678,2	K562	blood:
12	chr4:93036522..93038692-chr4:93040395..93042762,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GRID2-2	chr4:92947431-92947539	NONHSAT097424
2	lnc-GRID2-2	chr4:92951738-92951863	NONHSAT097424

Variant related genes	Relation type
ENSG00000256889	TF binding region
ENSG00000202077	chromatin interactions
ENSG00000143420	chromatin interactions

Extended variants
information (count: 2291 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:2291 , 50 per page) page: 1 2 3 4 5 6 7 ... 46

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs13148117	chr4:92908698-92908699	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs370560040	chr4:92908757-92908758	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs34338191	chr4:92908760-92908761	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs187349531	chr4:92908786-92908787	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs551701907	chr4:92908795-92908796	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs566901549	chr4:92908870-92908871	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs568384894	chr4:92908901-92908902	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs557066622	chr4:92908964-92908965	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs577231307	chr4:92909005-92909006	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs193193084	chr4:92909026-92909027	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs534413413	chr4:92909099-92909100	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs184679244	chr4:92909116-92909117	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs572258474	chr4:92909141-92909142	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs541375262	chr4:92909147-92909148	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs543020996	chr4:92909195-92909196	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs561148394	chr4:92909206-92909207	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs552757807	chr4:92909217-92909218	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs13125360	chr4:92909231-92909232	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs189951784	chr4:92909307-92909308	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs563262176	chr4:92909315-92909316	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs572574320	chr4:92911019-92911020	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs542020538	chr4:92911072-92911073	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs561760582	chr4:92911084-92911085	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs529330017	chr4:92911086-92911087	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs561903885	chr4:92911116-92911117	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs74460416	chr4:92911120-92911121	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs145605270	chr4:92911135-92911136	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs114092448	chr4:92911136-92911137	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs28396167	chr4:92911241-92911242	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs191520596	chr4:92911247-92911248	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs113580091	chr4:92911366-92911367	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs182097444	chr4:92911422-92911423	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs186247214	chr4:92911427-92911428	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs7695964	chr4:92911433-92911434	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs536824365	chr4:92911499-92911500	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs550885235	chr4:92911510-92911511	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs551616884	chr4:92911513-92911514	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs146987629	chr4:92911518-92911519	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs374410566	chr4:92911519-92911520	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs539438881	chr4:92911620-92911621	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs28830009	chr4:92911634-92911635	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs191490365	chr4:92911704-92911705	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs77032036	chr4:92911733-92911734	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs527853000	chr4:92911740-92911741	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs77086686	chr4:92911759-92911760	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs555038069	chr4:92911779-92911780	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs575820681	chr4:92911791-92911792	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs77066733	chr4:92911823-92911824	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs74579830	chr4:92911824-92911825	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs544447466	chr4:92911847-92911848	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:87)

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
Obesity	20622171	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Cancer	20164920	CNVD
Cancer	20164919	CNVD
Esophageal cancer	21851588	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Cancer	19907438	CNVD

Chromatin state (count:161 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:92911000-92912000	Enhancers	Stomach Mucosa	stomach
2	chr4:92923000-92923600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr4:92931600-92931800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr4:92931800-92932400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr4:92932400-92934000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr4:92934000-92934600	Enhancers	Stomach Mucosa	stomach
7	chr4:92934000-92935000	Enhancers	Fetal Lung	lung
8	chr4:92934000-92935200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr4:92934200-92934400	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
10	chr4:92934200-92934400	Active TSS	Duodenum Mucosa	Duodenum
11	chr4:92934400-92934600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
12	chr4:92934400-92934600	Flanking Active TSS	Duodenum Mucosa	Duodenum
13	chr4:92934400-92934600	Enhancers	Duodenum Smooth Muscle	Duodenum
14	chr4:92934400-92934600	Enhancers	Gastric	stomach
15	chr4:92934400-92934600	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
16	chr4:92934400-92934800	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
17	chr4:92934400-92934800	Active TSS	HUES6 Cell Line	embryonic stem cell
18	chr4:92934400-92934800	Active TSS	HUES64 Cell Line	embryonic stem cell
19	chr4:92934400-92934800	Enhancers	Small Intestine	intestine
20	chr4:92934400-92935000	Enhancers	H1 Cell Line	embryonic stem cell
21	chr4:92934400-92935000	Enhancers	HepG2	liver
22	chr4:92934400-92935200	Enhancers	iPS-18 Cell Line	embryonic stem cell
23	chr4:92934400-92935200	Enhancers	Liver	Liver
24	chr4:92934400-92935400	Enhancers	Rectal Mucosa Donor 31	rectum
25	chr4:92934600-92934800	Enhancers	Duodenum Mucosa	Duodenum
26	chr4:92934600-92934800	Active TSS	Rectal Mucosa Donor 29	rectum
27	chr4:92934600-92935600	Weak transcription	Stomach Mucosa	stomach
28	chr4:92934800-92935200	Enhancers	HUES48 Cell Line	embryonic stem cell
29	chr4:92934800-92935200	Weak transcription	Duodenum Mucosa	Duodenum
30	chr4:92934800-92935200	Enhancers	Fetal Intestine Small	intestine
31	chr4:92934800-92935200	Weak transcription	Small Intestine	intestine
32	chr4:92934800-92935600	Enhancers	Fetal Intestine Large	intestine
33	chr4:92934800-92936800	Enhancers	Rectal Mucosa Donor 29	rectum
34	chr4:92935000-92936000	Weak transcription	Fetal Lung	lung
35	chr4:92935200-92935600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr4:92935200-92935600	Enhancers	Small Intestine	intestine
37	chr4:92935200-92936000	Enhancers	Duodenum Mucosa	Duodenum
38	chr4:92935400-92935600	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
39	chr4:92935600-92935800	Enhancers	Stomach Mucosa	stomach
40	chr4:92935600-92936400	Weak transcription	Fetal Intestine Large	intestine
41	chr4:92935600-92936800	Enhancers	Rectal Mucosa Donor 31	rectum
42	chr4:92935800-92936200	Weak transcription	Stomach Mucosa	stomach
43	chr4:92936000-92936200	Enhancers	Fetal Lung	lung
44	chr4:92936200-92936600	Enhancers	Stomach Mucosa	stomach
45	chr4:92936600-92936800	Enhancers	Fetal Intestine Large	intestine
46	chr4:92936800-92949200	Weak transcription	Rectal Mucosa Donor 31	rectum
47	chr4:92941800-92943600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr4:92944000-92946600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr4:92947600-92948000	Active TSS	ES-I3 Cell Line	embryonic stem cell
50	chr4:92947600-92948000	Active TSS	ES-WA7 Cell Line	embryonic stem cell

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