Variant report

Variant	nsv537110
Chromosome Location	chr4:62398737-62553769
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:456)
CpG islands
(count:245)
Chromatin interactive
region (count:4)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:456 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr4:62409692-62410025	IMR90	lung:	n/a	chr4:62409858-62409869
2	CEBPB	chr4:62430784-62430963	HepG2	liver:	n/a	n/a
3	CEBPB	chr4:62409839-62409879	K562	blood:	n/a	chr4:62409858-62409869
4	CEBPB	chr4:62409705-62410030	HepG2	liver:	n/a	chr4:62409858-62409869
5	CEBPB	chr4:62423536-62423854	HepG2	liver:	n/a	chr4:62423678-62423689 chr4:62423679-62423688
6	CEBPB	chr4:62415109-62415428	H1-hESC	embryonic stem cell:	n/a	chr4:62415282-62415293
7	CEBPB	chr4:62504343-62504736	IMR90	lung:	n/a	n/a
8	CEBPB	chr4:62415124-62415402	HepG2	liver:	n/a	chr4:62415282-62415293
9	CEBPB	chr4:62423565-62423806	A549	lung:	n/a	chr4:62423678-62423689 chr4:62423679-62423688
10	CEBPB	chr4:62409708-62410057	Hela-S3	cervix:	n/a	chr4:62409858-62409869
11	CEBPB	chr4:62415121-62415437	IMR90	lung:	n/a	chr4:62415282-62415293
12	CHD2	chr4:62419561-62419787	H1-hESC	embryonic stem cell:	n/a	n/a
13	CTCF	chr4:62456680-62456830	HRPEpiC	eye:	n/a	n/a
14	CTCF	chr4:62456700-62456850	HCFaa	heart:	n/a	n/a
15	CTCF	chr4:62406760-62406910	HEEpiC	esophagus:	n/a	n/a
16	CTCF	chr4:62407320-62407470	HMEC	breast:	n/a	n/a
17	CTCF	chr4:62485300-62485450	Hela-S3	cervix:	n/a	n/a
18	CTCF	chr4:62407273-62407492	LNCaP	prostate:	n/a	n/a
19	CTCF	chr4:62456720-62456870	GM12878	blood:	n/a	n/a
20	CTCF	chr4:62485320-62485470	SK-N-SH_RA	brain:	n/a	n/a
21	CTCF	chr4:62456660-62456810	HEEpiC	esophagus:	n/a	n/a
22	CTCF	chr4:62406829-62406914	Pancreas_OC	pancreas:	n/a	n/a
23	CTCF	chr4:62485300-62485450	RPTEC	kidney:	n/a	n/a
24	CTCF	chr4:62456720-62456870	WERI-Rb-1	eye:	n/a	n/a
25	CTCF	chr4:62456620-62456770	A549	lung:	n/a	n/a
26	CTCF	chr4:62485360-62485510	HPAF	blood vessel:	n/a	n/a
27	CTCF	chr4:62407260-62407410	NHEK	skin:	n/a	n/a
28	CTCF	chr4:62456700-62456850	HepG2	liver:	n/a	n/a
29	CTCF	chr4:62485426-62485445	A549	lung:	n/a	n/a
30	CTCF	chr4:62456720-62456870	HCPEpiC	choroid plexus:	n/a	n/a
31	CTCF	chr4:62407340-62407490	HA-sp	spinal cord:	n/a	n/a
32	CTCF	chr4:62456716-62456875	NHEK	skin:	n/a	n/a
33	CTCF	chr4:62485380-62485514	Gliobla	brain:	n/a	n/a
34	CTCF	chr4:62456740-62456890	Caco-2	colon:	n/a	n/a
35	CTCF	chr4:62485200-62485350	HA-sp	spinal cord:	n/a	n/a
36	CTCF	chr4:62485340-62485490	HRE	kidney:	n/a	n/a
37	CTCF	chr4:62485340-62485490	HPF	lung:	n/a	n/a
38	CTCF	chr4:62485440-62485590	HA-sp	spinal cord:	n/a	n/a
39	CTCF	chr4:62456680-62456830	AoAF	blood vessel:	n/a	n/a
40	CTCF	chr4:62456760-62456910	HA-sp	spinal cord:	n/a	n/a
41	CTCF	chr4:62456631-62456964	GM12878	blood:	n/a	n/a
42	CTCF	chr4:62456760-62456910	HPAF	blood vessel:	n/a	n/a
43	CTCF	chr4:62407372-62407402	HUVEC	blood vessel:	n/a	n/a
44	CTCF	chr4:62485360-62485510	MCF-7	breast:	n/a	n/a
45	CTCF	chr4:62485380-62485530	HL-60	blood:	n/a	n/a
46	CTCF	chr4:62456640-62456790	HRPEpiC	eye:	n/a	n/a
47	CTCF	chr4:62407340-62407490	SK-N-SH_RA	brain:	n/a	n/a
48	CTCF	chr4:62485380-62485530	NHDF-neo	bronchial:	n/a	n/a
49	CTCF	chr4:62407258-62407554	GM12878	blood:	n/a	n/a
50	CTCF	chr4:62485280-62485613	GM12878	blood:	n/a	n/a

(count:245 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:62512765-62512815	HRCEpiC	kidney:	n/a
2	chr4:62512765-62512815	HRCEpiC	kidney:	n/a
3	chr4:62512765-62512815	BJ	skin:	n/a
4	chr4:62512765-62512815	HCT-116	colon:	n/a
5	chr4:62450110-62450160	AG04449	skin:	fetal
6	chr4:62512735-62512785	Caco-2	colon:	n/a
7	chr4:62467955-62468005	A549	lung:	n/a
8	chr4:62467955-62468005	SK-N-SH	brain:	n/a
9	chr4:62512765-62512815	NT2-D1	testis:	n/a
10	chr4:62450110-62450160	Caco-2	colon:	n/a
11	chr4:62512735-62512785	K562	blood:	n/a
12	chr4:62467955-62468005	PrEC	prostate:	n/a
13	chr4:62450110-62450160	GM19239	blood:	n/a
14	chr4:62450110-62450160	AG10803	skin:	n/a
15	chr4:62467955-62468005	GM19239	blood:	n/a
16	chr4:62467955-62468005	AG10803	skin:	n/a
17	chr4:62512765-62512815	HCPEpiC	choroid plexus:	n/a
18	chr4:62450110-62450160	GM12891	blood:	n/a
19	chr4:62512765-62512815	HIPEpiC	eye:	n/a
20	chr4:62467955-62468005	ProgFib	skin:	n/a
21	chr4:62512735-62512785	HRPEpiC	eye:	n/a
22	chr4:62450110-62450160	SAEC	small airway:	n/a
23	chr4:62512735-62512785	Jurkat	blood:	n/a
24	chr4:62450110-62450160	NHBE	bronchial:	n/a
25	chr4:62450110-62450160	GM12892	blood:	n/a
26	chr4:62467955-62468005	GM06990	blood:	n/a
27	chr4:62512765-62512815	HL-60	blood:	n/a
28	chr4:62450110-62450160	CMK	blood:	n/a
29	chr4:62512735-62512785	SK-N-SH	brain:	n/a
30	chr4:62450110-62450160	MCF10A-Er-Src	breast:	n/a
31	chr4:62512735-62512785	LNCaP	prostate:	n/a
32	chr4:62512765-62512815	HRE	kidney:	n/a
33	chr4:62512735-62512785	A549	lung:	n/a
34	chr4:62467955-62468005	BE2_C	brain:	n/a
35	chr4:62512735-62512785	AG04449	skin:	fetal
36	chr4:62450110-62450160	HCT-116	colon:	n/a
37	chr4:62512765-62512815	ProgFib	skin:	n/a
38	chr4:62467955-62468005	SK-N-MC	brain:	n/a
39	chr4:62467955-62468005	HPAEpiC	pulmonary alveolar:	n/a
40	chr4:62512765-62512815	BE2_C	brain:	n/a
41	chr4:62467955-62468005	NHBE	bronchial:	n/a
42	chr4:62450110-62450160	HL-60	blood:	n/a
43	chr4:62467955-62468005	ovcar-3	ovarian:	n/a
44	chr4:62512735-62512785	ProgFib	skin:	n/a
45	chr4:62512765-62512815	AG04450	lung:	fetal
46	chr4:62512765-62512815	HCM	heart:	n/a
47	chr4:62450110-62450160	NT2-D1	testis:	n/a
48	chr4:62512765-62512815	HCF	heart:	n/a
49	chr4:62450110-62450160	HRPEpiC	eye:	n/a
50	chr4:62512735-62512785	T-47D	breast:	n/a

(count:4 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:62525228..62527571-chr4:62528820..62531208,2	K562	blood:
2	chr4:62525228..62527571-chr4:62528820..62531208,2	K562	blood:
3	chr4:61730714..61731311-chr4:62456306..62456868,3	MCF-7	breast:
4	chr20:55609055..55611493-chr4:62549876..62551792,2	MCF-7	breast:

No data

Variant related genes	Relation type
LPHN3	TF binding region
LPHN3	CpG island

Extended variants
information (count: 4677 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:4677 , 50 per page) page: 1 2 3 4 5 6 7 ... 94

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs565188344	chr4:62398782-62398783	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs182792818	chr4:62398785-62398786	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs547644643	chr4:62398789-62398790	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs574011519	chr4:62398794-62398795	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs377563665	chr4:62398807-62398808	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs370383406	chr4:62398837-62398838	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs535502080	chr4:62398892-62398893	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs530398000	chr4:62398909-62398910	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs6813884	chr4:62398938-62398939	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs573316345	chr4:62398944-62398945	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs376850531	chr4:62398985-62398986	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs536995747	chr4:62399063-62399064	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs558626991	chr4:62399132-62399133	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs559646901	chr4:62399164-62399165	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs187078436	chr4:62399173-62399174	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs11374089	chr4:62399191-62399192	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs397709967	chr4:62399199-62399200	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs144044868	chr4:62399227-62399228	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs368191804	chr4:62399228-62399229	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs17226207	chr4:62399244-62399245	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs552870167	chr4:62399250-62399251	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs545230816	chr4:62399268-62399269	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs541710237	chr4:62399275-62399276	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs554591013	chr4:62399279-62399280	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs192943309	chr4:62399319-62399320	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs183537013	chr4:62399321-62399322	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs188810821	chr4:62399322-62399323	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs543411326	chr4:62399412-62399413	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs577623870	chr4:62399448-62399449	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs565397449	chr4:62399498-62399499	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs55773246	chr4:62399499-62399500	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs541640280	chr4:62399530-62399531	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs559973079	chr4:62399563-62399564	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs193300258	chr4:62399564-62399565	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs76655004	chr4:62399646-62399647	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs184670469	chr4:62399661-62399662	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs530533390	chr4:62399665-62399666	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs551858666	chr4:62399705-62399706	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs570554077	chr4:62399715-62399716	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs530501804	chr4:62399745-62399746	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs534403402	chr4:62399800-62399801	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs146638526	chr4:62399841-62399842	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs567913425	chr4:62399856-62399857	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs535227823	chr4:62399857-62399858	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs556847771	chr4:62399886-62399887	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs368546211	chr4:62399897-62399898	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs141469587	chr4:62399903-62399904	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs75233794	chr4:62399909-62399910	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs188293420	chr4:62399918-62399919	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs554098826	chr4:62399935-62399936	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:92)

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
T-cell prolymphocytic leukemia	19278963	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
small cell lung cancer	20016488	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute myeloid leukemia	21251322	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute myeloid leukemia	20729466	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
Ewing''s sarcoma	17952124	CNVD
Acute monocytic leukemia	16498392	CNVD
Prostate cancer	16573809	CNVD
Osteoporosis	18992858	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Breast cancer	20369283	CNVD
Anaplastic thyroid cancer	18753363	CNVD
Cancer	20164919	CNVD
Lung cancer	20668451	CNVD
Intellectual disability	21811512	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Pancreatic cancer	17952125	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Breast cancer	22522925	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Myelodysplastic syndrome	21251322	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:426 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:62397000-62398800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr4:62397000-62399200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr4:62397000-62406800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
4	chr4:62397800-62398800	Enhancers	Brain Substantia Nigra	brain
5	chr4:62397800-62399000	Enhancers	Brain Angular Gyrus	brain
6	chr4:62397800-62399000	Enhancers	Fetal Kidney	kidney
7	chr4:62397800-62399200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
8	chr4:62397800-62399200	Enhancers	Placenta Amnion	Placenta Amnion
9	chr4:62398200-62399000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
10	chr4:62398200-62399000	Enhancers	HMEC	breast
11	chr4:62398400-62398800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
12	chr4:62398400-62398800	Enhancers	Brain Inferior Temporal Lobe	brain
13	chr4:62398400-62399000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr4:62398400-62399000	Enhancers	NHEK	skin
15	chr4:62398400-62399200	Enhancers	Fetal Intestine Small	intestine
16	chr4:62398400-62399200	Enhancers	NH-A	brain
17	chr4:62398600-62398800	Enhancers	Brain Anterior Caudate	brain
18	chr4:62398600-62404800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
19	chr4:62398600-62404800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr4:62398600-62404800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
21	chr4:62398800-62399200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
22	chr4:62399200-62404800	Weak transcription	Fetal Intestine Small	intestine
23	chr4:62404400-62405800	Enhancers	Fetal Heart	heart
24	chr4:62404800-62405000	Enhancers	Left Ventricle	heart
25	chr4:62404800-62405200	Enhancers	Right Atrium	heart
26	chr4:62404800-62405600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
27	chr4:62404800-62406200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr4:62404800-62406800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
29	chr4:62404800-62408000	Enhancers	Fetal Intestine Small	intestine
30	chr4:62405400-62408400	Enhancers	Fetal Intestine Large	intestine
31	chr4:62405600-62406800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
32	chr4:62405800-62406200	Weak transcription	Fetal Heart	heart
33	chr4:62405800-62406400	Enhancers	Stomach Mucosa	stomach
34	chr4:62406000-62407600	Enhancers	Rectal Mucosa Donor 29	rectum
35	chr4:62406200-62406800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr4:62406200-62407600	Enhancers	Fetal Heart	heart
37	chr4:62406400-62406800	Weak transcription	Stomach Mucosa	stomach
38	chr4:62406400-62407000	Enhancers	HUES6 Cell Line	embryonic stem cell
39	chr4:62406400-62407000	Enhancers	iPS-20b Cell Line	embryonic stem cell
40	chr4:62406400-62407400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr4:62406400-62407400	Enhancers	Duodenum Mucosa	Duodenum
42	chr4:62406400-62407600	Enhancers	iPS-18 Cell Line	embryonic stem cell
43	chr4:62406400-62408000	Enhancers	Rectal Mucosa Donor 31	rectum
44	chr4:62406600-62407000	Enhancers	iPS-15b Cell Line	embryonic stem cell
45	chr4:62406600-62407000	Enhancers	Fetal Lung	lung
46	chr4:62406600-62407400	Enhancers	ES-I3 Cell Line	embryonic stem cell
47	chr4:62406600-62407400	Enhancers	HUES48 Cell Line	embryonic stem cell
48	chr4:62406600-62407400	Enhancers	HUES64 Cell Line	embryonic stem cell
49	chr4:62406600-62407600	Enhancers	HepG2	liver
50	chr4:62406800-62407000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links