Variant report

Variant	nsv470389
Chromosome Location	chr7:123893808-123936486
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	ATF1	chr7:123909888-123910120	K562	blood:	n/a	n/a
2	ATF1	chr7:123903518-123903832	K562	blood:	n/a	n/a
3	ATF2	chr7:123897573-123898594	GM12878	blood:	n/a	n/a
4	ATF2	chr7:123903345-123903808	GM12878	blood:	n/a	n/a
5	ATF3	chr7:123903532-123903773	GM12878	blood:	n/a	n/a
6	ATF3	chr7:123903568-123903806	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF3	chr7:123903479-123903869	H1-hESC	embryonic stem cell:	n/a	n/a
8	BATF	chr7:123897707-123898119	GM12878	blood:	n/a	chr7:123897898-123897908 chr7:123897902-123897912 chr7:123897901-123897912
9	BATF	chr7:123903526-123903804	GM12878	blood:	n/a	n/a
10	BATF	chr7:123903522-123903804	GM12878	blood:	n/a	n/a
11	BCLAF1	chr7:123897642-123898236	GM12878	blood:	n/a	chr7:123898197-123898206 chr7:123897901-123897910
12	BHLHE40	chr7:123903573-123903692	GM12878	blood:	n/a	n/a
13	BRCA1	chr7:123915746-123915818	H1-hESC	embryonic stem cell:	n/a	n/a
14	CEBPB	chr7:123903391-123903997	GM12878	blood:	n/a	chr7:123903693-123903704
15	CEBPB	chr7:123915569-123915830	HepG2	liver:	n/a	chr7:123915698-123915709 chr7:123915698-123915711
16	CEBPB	chr7:123903529-123903831	A549	lung:	n/a	chr7:123903693-123903704
17	CEBPB	chr7:123903360-123903944	H1-hESC	embryonic stem cell:	n/a	chr7:123903693-123903704
18	CEBPB	chr7:123903490-123903892	IMR90	lung:	n/a	chr7:123903693-123903704
19	CEBPB	chr7:123903581-123903839	K562	blood:	n/a	chr7:123903693-123903704
20	CEBPB	chr7:123903472-123904002	HCT-116	colon:	n/a	chr7:123903693-123903704
21	CEBPB	chr7:123915528-123915868	H1-hESC	embryonic stem cell:	n/a	chr7:123915698-123915709 chr7:123915698-123915711
22	CEBPB	chr7:123903524-123903881	HepG2	liver:	n/a	chr7:123903693-123903704
23	CEBPB	chr7:123903383-123903885	HCT-116	colon:	n/a	chr7:123903693-123903704
24	CEBPB	chr7:123903628-123903761	K562	blood:	n/a	chr7:123903693-123903704
25	CEBPB	chr7:123901777-123902073	H1-hESC	embryonic stem cell:	n/a	n/a
26	CEBPB	chr7:123903512-123903887	Hela-S3	cervix:	n/a	chr7:123903693-123903704
27	CHD1	chr7:123903538-123903727	GM12878	blood:	n/a	n/a
28	CTCF	chr7:123916180-123916330	HepG2	liver:	n/a	chr7:123916248-123916257
29	CTCF	chr7:123916140-123916290	BE2_C	brain:	n/a	chr7:123916248-123916257 chr7:123916179-123916197
30	CTCF	chr7:123916180-123916330	A549	lung:	n/a	chr7:123916248-123916257
31	CTCF	chr7:123916082-123916420	ECC-1	luminal epithelium:	n/a	chr7:123916248-123916257 chr7:123916179-123916197
32	CTCF	chr7:123915680-123915830	GM12864	blood:	n/a	n/a
33	CTCF	chr7:123916300-123916450	WI-38	lung:	n/a	n/a
34	CTCF	chr7:123916200-123916350	GM12869	blood:	n/a	chr7:123916248-123916257
35	CTCF	chr7:123903180-123903330	AG04450	lung:	n/a	n/a
36	CTCF	chr7:123916220-123916370	GM12866	blood:	n/a	chr7:123916248-123916257
37	CTCF	chr7:123916180-123916330	GM12865	blood:	n/a	chr7:123916248-123916257
38	CTCF	chr7:123916180-123916329	GM20000	blood:	n/a	chr7:123916248-123916257
39	CTCF	chr7:123915800-123915950	HMEC	breast:	n/a	n/a
40	CTCF	chr7:123916073-123916418	K562	blood:	n/a	chr7:123916248-123916257 chr7:123916179-123916197
41	CTCF	chr7:123916180-123916330	GM12872	blood:	n/a	chr7:123916248-123916257
42	CTCF	chr7:123916180-123916330	SAEC	small airway:	n/a	chr7:123916248-123916257
43	CTCF	chr7:123915851-123916821	SK-N-SH	brain:	n/a	chr7:123916248-123916257 chr7:123916179-123916197
44	CTCF	chr7:123916175-123916417	GM19240	blood:	n/a	chr7:123916248-123916257 chr7:123916179-123916197
45	CTCF	chr7:123916160-123916310	SK-N-SH_RA	brain:	n/a	chr7:123916248-123916257 chr7:123916179-123916197
46	CTCF	chr7:123916138-123916402	MCF-7	breast:	n/a	chr7:123916248-123916257 chr7:123916179-123916197
47	CTCF	chr7:123903160-123903310	GM12872	blood:	n/a	n/a
48	CTCF	chr7:123916220-123916370	MCF-7	breast:	n/a	chr7:123916248-123916257
49	CTCF	chr7:123916220-123916370	AoAF	blood vessel:	n/a	chr7:123916248-123916257
50	CTCF	chr7:123903280-123903430	AG04450	lung:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:123903317-123903367	HRPEpiC	eye:	n/a
2	chr7:123903317-123903367	HMEC	breast:	n/a
3	chr7:123916407-123916457	HRE	kidney:	n/a
4	chr7:123903317-123903367	SKMC	muscle:	n/a
5	chr7:123903317-123903367	AG04449	skin:	fetal
6	chr7:123916407-123916457	GM12891	blood:	n/a
7	chr7:123916407-123916457	GM12892	blood:	n/a
8	chr7:123903317-123903367	SK-N-SH_RA	brain:	n/a
9	chr7:123916407-123916457	HEEpiC	esophagus:	n/a
10	chr7:123903317-123903367	GM12878	blood:	n/a
11	chr7:123903317-123903367	AG04450	lung:	fetal
12	chr7:123916407-123916457	AG04450	lung:	fetal
13	chr7:123903317-123903367	MCF-7	breast:	n/a
14	chr7:123916407-123916457	SAEC	small airway:	n/a
15	chr7:123903317-123903367	T-47D	breast:	n/a
16	chr7:123903317-123903367	HEEpiC	esophagus:	n/a
17	chr7:123903317-123903367	RPTEC	kidney:	n/a
18	chr7:123903317-123903367	PrEC	prostate:	n/a
19	chr7:123916407-123916457	H1-hESC	embryonic stem cell:	embryo
20	chr7:123903317-123903367	HL-60	blood:	n/a
21	chr7:123916407-123916457	AoSMC	blood vessel:	n/a
22	chr7:123916407-123916457	AG04449	skin:	fetal
23	chr7:123903317-123903367	HNPCEpiC	eye:	n/a
24	chr7:123903317-123903367	GM12892	blood:	n/a
25	chr7:123916407-123916457	HCT-116	colon:	n/a
26	chr7:123903317-123903367	HCM	heart:	n/a
27	chr7:123903317-123903367	H1-hESC	embryonic stem cell:	embryo
28	chr7:123916407-123916457	HNPCEpiC	eye:	n/a
29	chr7:123903317-123903367	ECC-1	luminal epithelium:	n/a
30	chr7:123903317-123903367	GM12891	blood:	n/a
31	chr7:123916407-123916457	HEK293	kidney:	embryo
32	chr7:123916407-123916457	HIPEpiC	eye:	n/a
33	chr7:123903317-123903367	NH-A	brain:	n/a
34	chr7:123916407-123916457	A549	lung:	n/a
35	chr7:123903317-123903367	MCF10A-Er-Src	breast:	n/a
36	chr7:123916407-123916457	K562	blood:	n/a
37	chr7:123903317-123903367	U87	brain:	n/a
38	chr7:123916407-123916457	AG09309	skin:	n/a
39	chr7:123903317-123903367	AG09309	skin:	n/a
40	chr7:123903317-123903367	PANC-1	pancreas:	n/a
41	chr7:123916407-123916457	MCF10A-Er-Src	breast:	n/a
42	chr7:123903317-123903367	BJ	skin:	n/a
43	chr7:123916407-123916457	NT2-D1	testis:	n/a
44	chr7:123916407-123916457	Jurkat	blood:	n/a
45	chr7:123916407-123916457	T-47D	breast:	n/a
46	chr7:123916407-123916457	HCM	heart:	n/a
47	chr7:123916407-123916457	Hepatocyte	liver:	n/a
48	chr7:123903317-123903367	ovcar-3	ovarian:	n/a
49	chr7:123916407-123916457	HRCEpiC	kidney:	n/a
50	chr7:123916407-123916457	ProgFib	skin:	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:123919958..123922914-chr7:123935794..123937294,2	K562	blood:
2	chr7:123915423..123917674-chr7:123921407..123924592,3	K562	blood:
3	chr7:123915423..123917674-chr7:123921407..123924592,3	K562	blood:
4	chr7:123892945..123894583-chr7:123896590..123898487,2	K562	blood:
5	chr7:123919958..123922914-chr7:123935794..123937294,2	K562	blood:
6	chr7:123892945..123894583-chr7:123896590..123898487,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TMEM229A-1	chr7:123927269-123927598	XLOC_006590
2	lnc-TMEM229A-1	chr7:123928853-123928879	NONHSAT123078
3	lnc-TMEM229A-1	chr7:123928853-123928911	NONHSAT123077
4	lnc-TMEM229A-1	chr7:123914775-123915052	NONHSAT123077
5	lnc-TMEM229A-1	chr7:123914733-123915052	XLOC_006590
6	lnc-TMEM229A-1	chr7:123914775-123915052	NONHSAT123078
7	lnc-TMEM229A-1	chr7:123927269-123927344	NONHSAT123078

Variant related genes	Relation type
ENSG00000243574	TF binding region
ENSG00000243574	CpG island
C6orf168	miRNA target sites

Extended variants
information (count: 1013 )
Associated
traits (count: 88 )

Variant overlapped rSNPs/rCNVs (count:1013 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs13232381	chr7:123893808-123893809	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs550168476	chr7:123893822-123893823	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs4427107	chr7:123893838-123893839	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs529422254	chr7:123893843-123893844	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs542714148	chr7:123893853-123893854	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs565584428	chr7:123893897-123893898	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs538578854	chr7:123893907-123893908	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs188039389	chr7:123893966-123893967	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs554969967	chr7:123893988-123893989	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs17146889	chr7:123894038-123894039	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs551228162	chr7:123894087-123894088	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs571541478	chr7:123894117-123894118	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs536620684	chr7:123894130-123894131	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs12669869	chr7:123894170-123894171	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs556950800	chr7:123894174-123894175	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs193071470	chr7:123894180-123894181	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs13245540	chr7:123894242-123894243	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs13245541	chr7:123894244-123894245	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs551207341	chr7:123894266-123894267	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs531456984	chr7:123894275-123894276	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs536400480	chr7:123894371-123894372	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs561448961	chr7:123894429-123894430	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs146370642	chr7:123894469-123894470	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs541658767	chr7:123894628-123894629	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs139161532	chr7:123894630-123894631	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs564594146	chr7:123894632-123894633	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs149907157	chr7:123894668-123894669	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs543437491	chr7:123894750-123894751	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs183634575	chr7:123894854-123894855	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs373047534	chr7:123894867-123894868	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs545774513	chr7:123894873-123894874	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs188235051	chr7:123894883-123894884	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs2159572	chr7:123894945-123894946	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs559437267	chr7:123894966-123894967	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs143845925	chr7:123894967-123894968	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs551191048	chr7:123894973-123894974	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs531911279	chr7:123895010-123895011	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs12706574	chr7:123895019-123895020	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs113799697	chr7:123895048-123895049	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs148623327	chr7:123895059-123895060	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs544447878	chr7:123895063-123895064	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs7799219	chr7:123895098-123895099	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
43	rs12706575	chr7:123895151-123895152	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs536264343	chr7:123895165-123895166	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs561052368	chr7:123895199-123895200	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs370659343	chr7:123895223-123895224	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs566591254	chr7:123895257-123895258	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs10254870	chr7:123895304-123895305	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs147858803	chr7:123895310-123895311	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs192730050	chr7:123895322-123895323	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:88)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Melanoma	18172304	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Squamous cell cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	17387387	CNVD
Low-grade fibromyxoid sarcoma	0	CNVD
Oligodendroglial tumors	17285580	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21264507	CNVD
Shwachman-Diamond syndrome	22934832	CNVD
Colorectal cancer	19359472	CNVD
Cutaneous malignant melanoma	17690212	CNVD
Leukemia	17361228	CNVD
Breast cancer	16461572	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Malignant melanoma	17690212	CNVD
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Multiple myeloma	17550852	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neurodevelopmental disorder	22521361	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Metanephric adenoma	20802469	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
Myelodysplastic syndrome	21251322	CNVD
Chronic myeloid leukemia	21384125	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
lymphocytic leukemia	21291569	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16573809	CNVD
Medulloblastoma	16783165	CNVD
Biliary cancer	19435499	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Prostate cancer	23792589	CNVD
Adenocarcinoma	21044232	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Non-small cell lung cancer	19889201	CNVD
Acute myeloid leukemia	18000384	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Metastatic melanoma	18483359	CNVD
Autism	18414403	CNVD
Autism	19401682	CNVD
Autism	19546859	CNVD
Schizophrenia	19546859	CNVD
Tourette syndrome	19546859	CNVD
Melanoma	19188590	CNVD
Hepatocellular carcinoma	16785998	CNVD
Glioblastoma multiforme	18628472	CNVD
Basal cell lymphoma	21115979	CNVD
Breast cancer	21509527	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Epilepsy	21635232	CNVD
Squamous cell cancer	20885788	CNVD
Myelofibrosis	22110671	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:94 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:123887200-123903600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr7:123891400-123903200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
3	chr7:123892200-123894400	Weak transcription	Fetal Heart	heart
4	chr7:123893200-123896000	Enhancers	Fetal Lung	lung
5	chr7:123894400-123894800	Enhancers	Fetal Stomach	stomach
6	chr7:123894400-123897400	Enhancers	Fetal Heart	heart
7	chr7:123894600-123895600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr7:123894800-123899600	Weak transcription	Fetal Stomach	stomach
9	chr7:123895000-123896400	Enhancers	Fetal Brain Male	brain
10	chr7:123896600-123896800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
11	chr7:123896800-123902000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
12	chr7:123897400-123897800	Flanking Active TSS	Fetal Heart	heart
13	chr7:123897400-123898200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
14	chr7:123897400-123898200	Enhancers	Hela-S3	cervix
15	chr7:123897800-123900600	Enhancers	Fetal Heart	heart
16	chr7:123898000-123898200	Enhancers	H9 Cell Line	embryonic stem cell
17	chr7:123898200-123907200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
18	chr7:123898400-123899800	Weak transcription	H9 Cell Line	embryonic stem cell
19	chr7:123898600-123899200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
20	chr7:123899600-123900000	Enhancers	Fetal Stomach	stomach
21	chr7:123899600-123901000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
22	chr7:123899800-123900000	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
23	chr7:123899800-123900000	Enhancers	H9 Cell Line	embryonic stem cell
24	chr7:123899800-123900200	Enhancers	ES-I3 Cell Line	embryonic stem cell
25	chr7:123900200-123901400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
26	chr7:123900600-123902000	Weak transcription	Fetal Heart	heart
27	chr7:123900800-123902200	Enhancers	iPS-15b Cell Line	embryonic stem cell
28	chr7:123901000-123902000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
29	chr7:123901000-123905000	Enhancers	iPS-18 Cell Line	embryonic stem cell
30	chr7:123901200-123904800	Enhancers	HUES6 Cell Line	embryonic stem cell
31	chr7:123901200-123905200	Enhancers	HUES48 Cell Line	embryonic stem cell
32	chr7:123901400-123904800	Enhancers	iPS-20b Cell Line	embryonic stem cell
33	chr7:123901400-123905000	Enhancers	HUES64 Cell Line	embryonic stem cell
34	chr7:123901400-123905200	Enhancers	ES-I3 Cell Line	embryonic stem cell
35	chr7:123901800-123903400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr7:123902000-123902200	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
37	chr7:123902000-123902200	Enhancers	H9 Cell Line	embryonic stem cell
38	chr7:123902000-123902200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
39	chr7:123902000-123902400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
40	chr7:123902000-123902400	Enhancers	Fetal Heart	heart
41	chr7:123902000-123904600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
42	chr7:123902200-123902600	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
43	chr7:123902200-123903200	Weak transcription	H9 Cell Line	embryonic stem cell
44	chr7:123902200-123904800	Enhancers	H1 Cell Line	embryonic stem cell
45	chr7:123902400-123904200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
46	chr7:123902800-123903200	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
47	chr7:123903200-123903800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
48	chr7:123903200-123903800	Enhancers	H9 Cell Line	embryonic stem cell
49	chr7:123903200-123903800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
50	chr7:123903200-123904400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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