Variant report

Variant	nsv879077
Chromosome Location	chr4:62419426-62545435
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:354)
CpG islands
(count:245)
Chromatin interactive
region (count:3)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:354 , 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	CEBPB	chr4:62430784-62430963	HepG2	liver:	n/a	n/a
2	CEBPB	chr4:62504343-62504736	IMR90	lung:	n/a	n/a
3	CEBPB	chr4:62423536-62423854	HepG2	liver:	n/a	chr4:62423678-62423689 chr4:62423679-62423688
4	CEBPB	chr4:62423565-62423806	A549	lung:	n/a	chr4:62423678-62423689 chr4:62423679-62423688
5	CHD2	chr4:62419561-62419787	H1-hESC	embryonic stem cell:	n/a	n/a
6	CTCF	chr4:62456718-62456855	MCF-7	breast:	n/a	n/a
7	CTCF	chr4:62456880-62457030	HRE	kidney:	n/a	n/a
8	CTCF	chr4:62485407-62485476	MCF-7	breast:	n/a	n/a
9	CTCF	chr4:62456560-62456710	SAEC	small airway:	n/a	n/a
10	CTCF	chr4:62456720-62456870	HPF	lung:	n/a	n/a
11	CTCF	chr4:62485300-62485450	HRPEpiC	eye:	n/a	n/a
12	CTCF	chr4:62456740-62456890	HMEC	breast:	n/a	n/a
13	CTCF	chr4:62485300-62485450	NHEK	skin:	n/a	n/a
14	CTCF	chr4:62456723-62456883	HepG2	liver:	n/a	n/a
15	CTCF	chr4:62485300-62485450	RPTEC	kidney:	n/a	n/a
16	CTCF	chr4:62485360-62485510	MCF-7	breast:	n/a	n/a
17	CTCF	chr4:62485200-62485350	HA-sp	spinal cord:	n/a	n/a
18	CTCF	chr4:62485340-62485490	HepG2	liver:	n/a	n/a
19	CTCF	chr4:62485340-62485490	SAEC	small airway:	n/a	n/a
20	CTCF	chr4:62456760-62456910	HA-sp	spinal cord:	n/a	n/a
21	CTCF	chr4:62456600-62456750	HRE	kidney:	n/a	n/a
22	CTCF	chr4:62456700-62456850	HepG2	liver:	n/a	n/a
23	CTCF	chr4:62485340-62485490	NHEK	skin:	n/a	n/a
24	CTCF	chr4:62456720-62456870	RPTEC	kidney:	n/a	n/a
25	CTCF	chr4:62456720-62456870	HCPEpiC	choroid plexus:	n/a	n/a
26	CTCF	chr4:62456680-62456830	HPF	lung:	n/a	n/a
27	CTCF	chr4:62456715-62456871	Hela-S3	cervix:	n/a	n/a
28	CTCF	chr4:62485380-62485530	SK-N-SH_RA	brain:	n/a	n/a
29	CTCF	chr4:62485320-62485470	BE2_C	brain:	n/a	n/a
30	CTCF	chr4:62485320-62485470	MCF-7	breast:	n/a	n/a
31	CTCF	chr4:62485340-62485490	HCPEpiC	choroid plexus:	n/a	n/a
32	CTCF	chr4:62485300-62485450	BE2_C	brain:	n/a	n/a
33	CTCF	chr4:62456620-62456770	RPTEC	kidney:	n/a	n/a
34	CTCF	chr4:62485380-62485530	HL-60	blood:	n/a	n/a
35	CTCF	chr4:62456620-62456770	A549	lung:	n/a	n/a
36	CTCF	chr4:62456640-62456790	HEEpiC	esophagus:	n/a	n/a
37	CTCF	chr4:62485320-62485470	HBMEC	blood vessel:	n/a	n/a
38	CTCF	chr4:62456740-62456890	NHEK	skin:	n/a	n/a
39	CTCF	chr4:62485320-62485574	H1-hESC	embryonic stem cell:	n/a	n/a
40	CTCF	chr4:62485320-62485470	WERI-Rb-1	eye:	n/a	n/a
41	CTCF	chr4:62485368-62485531	H1-hESC	embryonic stem cell:	n/a	n/a
42	CTCF	chr4:62456660-62456810	WERI-Rb-1	eye:	n/a	n/a
43	CTCF	chr4:62485360-62485510	GM12867	blood:	n/a	n/a
44	CTCF	chr4:62485360-62485510	GM12878	blood:	n/a	n/a
45	CTCF	chr4:62485340-62485490	HCM	heart:	n/a	n/a
46	CTCF	chr4:62456720-62456870	HCM	heart:	n/a	n/a
47	CTCF	chr4:62456748-62456847	GM13977	blood:	n/a	n/a
48	CTCF	chr4:62485422-62485443	Hela-S3	cervix:	n/a	n/a
49	CTCF	chr4:62485380-62485530	Caco-2	colon:	n/a	n/a
50	CTCF	chr4:62485340-62485490	HA-sp	spinal cord:	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	SK-N-SH	brain:	n/a
2	chr4:62512765-62512815	SK-N-SH	brain:	n/a
3	chr4:62512765-62512815	HAEpiC	amniotic membrane:	n/a
4	chr4:62467955-62468005	MCF-7	breast:	n/a
5	chr4:62450110-62450160	NH-A	brain:	n/a
6	chr4:62467955-62468005	A549	lung:	n/a
7	chr4:62467955-62468005	MCF10A-Er-Src	breast:	n/a
8	chr4:62512765-62512815	HCT-116	colon:	n/a
9	chr4:62450110-62450160	MCF-7	breast:	n/a
10	chr4:62512735-62512785	PrEC	prostate:	n/a
11	chr4:62512735-62512785	A549	lung:	n/a
12	chr4:62450110-62450160	SK-N-MC	brain:	n/a
13	chr4:62450110-62450160	SAEC	small airway:	n/a
14	chr4:62467955-62468005	SK-N-SH_RA	brain:	n/a
15	chr4:62450110-62450160	GM19239	blood:	n/a
16	chr4:62512765-62512815	A549	lung:	n/a
17	chr4:62467955-62468005	IMR90	lung:	fetal
18	chr4:62512765-62512815	GM12892	blood:	n/a
19	chr4:62512735-62512785	GM12891	blood:	n/a
20	chr4:62467955-62468005	Hela-S3	cervix:	n/a
21	chr4:62512735-62512785	HCT-116	colon:	n/a
22	chr4:62512765-62512815	NT2-D1	testis:	n/a
23	chr4:62512735-62512785	IMR90	lung:	fetal
24	chr4:62512765-62512815	SKMC	muscle:	n/a
25	chr4:62467955-62468005	BE2_C	brain:	n/a
26	chr4:62512735-62512785	ProgFib	skin:	n/a
27	chr4:62467955-62468005	HPAEpiC	pulmonary alveolar:	n/a
28	chr4:62512735-62512785	HNPCEpiC	eye:	n/a
29	chr4:62450110-62450160	NB4	blood:	n/a
30	chr4:62467955-62468005	GM12878	blood:	n/a
31	chr4:62512735-62512785	NHBE	bronchial:	n/a
32	chr4:62512735-62512785	NHDF-neo	bronchial:	n/a
33	chr4:62467955-62468005	HUVEC	blood vessel:	n/a
34	chr4:62512765-62512815	AoSMC	blood vessel:	n/a
35	chr4:62467955-62468005	NB4	blood:	n/a
36	chr4:62450110-62450160	GM12878	blood:	n/a
37	chr4:62512735-62512785	SK-N-SH	brain:	n/a
38	chr4:62450110-62450160	AG09309	skin:	n/a
39	chr4:62512765-62512815	HEEpiC	esophagus:	n/a
40	chr4:62512765-62512815	HPAEpiC	pulmonary alveolar:	n/a
41	chr4:62467955-62468005	HCM	heart:	n/a
42	chr4:62450110-62450160	ovcar-3	ovarian:	n/a
43	chr4:62450110-62450160	RPTEC	kidney:	n/a
44	chr4:62450110-62450160	BE2_C	brain:	n/a
45	chr4:62450110-62450160	K562	blood:	n/a
46	chr4:62450110-62450160	GM12891	blood:	n/a
47	chr4:62512735-62512785	HPAEpiC	pulmonary alveolar:	n/a
48	chr4:62512735-62512785	HAEpiC	amniotic membrane:	n/a
49	chr4:62512765-62512815	SK-N-MC	brain:	n/a
50	chr4:62512765-62512815	HIPEpiC	eye:	n/a

(count:3 , 50 per page) page: 1

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

No data

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

Extended variants
information (count: 3586 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:3586 , 50 per page) page: 1 2 3 4 5 6 7 ... 72

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2343249	chr4:62419426-62419427	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs563766498	chr4:62419447-62419448	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs531066677	chr4:62419527-62419528	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs117622384	chr4:62419532-62419533	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs373057858	chr4:62419630-62419631	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs73822652	chr4:62419684-62419685	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs528750772	chr4:62419707-62419708	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs144987613	chr4:62419711-62419712	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs549536469	chr4:62419732-62419733	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs10015095	chr4:62419782-62419783	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs557174704	chr4:62419815-62419816	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs34976733	chr4:62419818-62419819	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs572096393	chr4:62419875-62419876	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs200517198	chr4:62419887-62419888	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs542145943	chr4:62419888-62419889	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs191183278	chr4:62419910-62419911	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs71211394	chr4:62419921-62419922	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs201603690	chr4:62419922-62419923	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs199570697	chr4:62419923-62419924	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs35087798	chr4:62419963-62419964	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs184061809	chr4:62419972-62419973	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs376138605	chr4:62419973-62419974	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs11731334	chr4:62419976-62419977	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs373324990	chr4:62419990-62419991	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs555374176	chr4:62419997-62419998	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs565675418	chr4:62420057-62420058	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs189426445	chr4:62420058-62420059	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs111955422	chr4:62420068-62420069	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs530999586	chr4:62420069-62420070	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs6836905	chr4:62420077-62420078	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs148133149	chr4:62420094-62420095	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs182004023	chr4:62420106-62420107	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs547019670	chr4:62420126-62420127	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs71607299	chr4:62420166-62420167	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs562035240	chr4:62420192-62420193	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs114643094	chr4:62420206-62420207	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs36095926	chr4:62420216-62420217	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs550741156	chr4:62420217-62420218	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs141953592	chr4:62420271-62420272	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs147308458	chr4:62420295-62420296	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs113085152	chr4:62420519-62420520	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs539484220	chr4:62420552-62420553	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs6813075	chr4:62420583-62420584	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs566416345	chr4:62420621-62420622	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs533548035	chr4:62420628-62420629	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs184982032	chr4:62420663-62420664	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs116024409	chr4:62420738-62420739	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs34250113	chr4:62420763-62420764	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs568229174	chr4:62420802-62420803	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs538165184	chr4:62420808-62420809	Weak transcription Enhancers	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:333 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:62407000-62421600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr4:62408000-62421200	Weak transcription	Fetal Intestine Small	intestine
3	chr4:62415200-62421600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr4:62416800-62421200	Weak transcription	Small Intestine	intestine
5	chr4:62417000-62421000	Weak transcription	Fetal Heart	heart
6	chr4:62417400-62420800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
7	chr4:62418800-62419600	Enhancers	iPS-15b Cell Line	embryonic stem cell
8	chr4:62418800-62419600	Enhancers	iPS-20b Cell Line	embryonic stem cell
9	chr4:62419200-62419600	Enhancers	HUES64 Cell Line	embryonic stem cell
10	chr4:62419200-62419800	Enhancers	ES-I3 Cell Line	embryonic stem cell
11	chr4:62419200-62419800	Enhancers	HUES48 Cell Line	embryonic stem cell
12	chr4:62419200-62419800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
13	chr4:62419200-62424600	Enhancers	Fetal Intestine Large	intestine
14	chr4:62419400-62419600	Enhancers	HUES6 Cell Line	embryonic stem cell
15	chr4:62419400-62419800	Enhancers	iPS-18 Cell Line	embryonic stem cell
16	chr4:62419400-62423400	Enhancers	Stomach Mucosa	stomach
17	chr4:62419600-62420400	Weak transcription	HUES6 Cell Line	embryonic stem cell
18	chr4:62419600-62420600	Weak transcription	HUES64 Cell Line	embryonic stem cell
19	chr4:62419600-62420600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
20	chr4:62419600-62425600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
21	chr4:62419800-62420600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
22	chr4:62419800-62421200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
23	chr4:62419800-62421200	Weak transcription	HUES48 Cell Line	embryonic stem cell
24	chr4:62419800-62421200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
25	chr4:62420400-62422200	Enhancers	HUES6 Cell Line	embryonic stem cell
26	chr4:62420600-62420800	Enhancers	HUES64 Cell Line	embryonic stem cell
27	chr4:62420600-62421800	Enhancers	iPS-15b Cell Line	embryonic stem cell
28	chr4:62420600-62422000	Enhancers	iPS-18 Cell Line	embryonic stem cell
29	chr4:62420800-62421400	Weak transcription	HUES64 Cell Line	embryonic stem cell
30	chr4:62420800-62424400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
31	chr4:62421000-62421800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr4:62421000-62423600	Enhancers	NH-A	brain
33	chr4:62421000-62423800	Enhancers	Fetal Heart	heart
34	chr4:62421200-62421400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
35	chr4:62421200-62421400	Enhancers	Left Ventricle	heart
36	chr4:62421200-62422000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
37	chr4:62421200-62422200	Enhancers	ES-I3 Cell Line	embryonic stem cell
38	chr4:62421200-62422200	Enhancers	HUES48 Cell Line	embryonic stem cell
39	chr4:62421200-62422200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
40	chr4:62421200-62422400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
41	chr4:62421200-62422400	Enhancers	Ovary	ovary
42	chr4:62421200-62422400	Enhancers	Rectal Mucosa Donor 31	rectum
43	chr4:62421200-62422600	Enhancers	Small Intestine	intestine
44	chr4:62421200-62423600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
45	chr4:62421200-62423600	Enhancers	Fetal Intestine Small	intestine
46	chr4:62421400-62422000	Enhancers	HUES64 Cell Line	embryonic stem cell
47	chr4:62421400-62422400	Enhancers	Placenta Amnion	Placenta Amnion
48	chr4:62421400-62423400	Enhancers	Duodenum Mucosa	Duodenum
49	chr4:62421600-62422200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
50	chr4:62421600-62422400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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