Variant report

Variant	nsv1017184
Chromosome Location	chr7:109240101-109350011
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	chr7:109288915-109288951	K562	blood:	n/a	n/a
2	ATF1	chr7:109299476-109299485	K562	blood:	n/a	n/a
3	BRCA1	chr7:109339733-109340007	Hela-S3	cervix:	n/a	n/a
4	CEBPB	chr7:109250552-109250777	Hela-S3	cervix:	n/a	n/a
5	CEBPB	chr7:109308764-109309015	HepG2	liver:	n/a	chr7:109308871-109308882
6	CEBPB	chr7:109287401-109287723	Hela-S3	cervix:	n/a	n/a
7	CEBPB	chr7:109277496-109277739	IMR90	lung:	n/a	n/a
8	CEBPB	chr7:109336388-109336670	HepG2	liver:	n/a	chr7:109336527-109336538
9	CEBPB	chr7:109250580-109250714	H1-hESC	embryonic stem cell:	n/a	n/a
10	CEBPB	chr7:109311157-109311365	HepG2	liver:	n/a	chr7:109311255-109311272 chr7:109311258-109311269 chr7:109311258-109311271 chr7:109311258-109311271 chr7:109311260-109311271
11	CEBPB	chr7:109334734-109335169	MCF-7	breast:	n/a	chr7:109334946-109334957 chr7:109334945-109334958
12	CEBPB	chr7:109334943-109335083	K562	blood:	n/a	chr7:109334946-109334957 chr7:109334945-109334958
13	CEBPB	chr7:109255089-109255375	HepG2	liver:	n/a	chr7:109255242-109255251 chr7:109255240-109255251 chr7:109255242-109255251 chr7:109255242-109255251 chr7:109255240-109255253 chr7:109255241-109255252 chr7:109255242-109255251 chr7:109255240-109255253
14	CEBPB	chr7:109334740-109335161	MCF-7	breast:	n/a	chr7:109334946-109334957 chr7:109334945-109334958
15	CEBPB	chr7:109334154-109335359	Hela-S3	cervix:	n/a	chr7:109334946-109334957 chr7:109334945-109334958
16	CEBPB	chr7:109284397-109284659	Hela-S3	cervix:	n/a	n/a
17	CEBPB	chr7:109336399-109336694	A549	lung:	n/a	chr7:109336527-109336538
18	CEBPB	chr7:109334780-109335046	HepG2	liver:	n/a	chr7:109334946-109334957 chr7:109334945-109334958
19	CEBPB	chr7:109286716-109286917	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr7:109334799-109335089	IMR90	lung:	n/a	chr7:109334946-109334957 chr7:109334945-109334958
21	CEBPB	chr7:109319356-109319661	K562	blood:	n/a	n/a
22	CEBPB	chr7:109339658-109340175	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr7:109336406-109337216	Hela-S3	cervix:	n/a	chr7:109336527-109336538
24	CEBPB	chr7:109255108-109255403	A549	lung:	n/a	chr7:109255242-109255251 chr7:109255240-109255251 chr7:109255242-109255251 chr7:109255242-109255251 chr7:109255240-109255253 chr7:109255241-109255252 chr7:109255242-109255251 chr7:109255240-109255253
25	CTCF	chr7:109292980-109293130	WERI-Rb-1	eye:	n/a	n/a
26	CTCF	chr7:109286743-109286828	LNCaP	prostate:	n/a	n/a
27	CTCF	chr7:109325695-109325776	GM10248	blood:	n/a	n/a
28	CTCF	chr7:109333900-109334050	BE2_C	brain:	n/a	n/a
29	CTCF	chr7:109333820-109333970	BE2_C	brain:	n/a	n/a
30	CTCF	chr7:109250574-109250658	GM12891	blood:	n/a	n/a
31	CTCF	chr7:109333840-109333990	SK-N-SH_RA	brain:	n/a	n/a
32	CTCF	chr7:109250601-109250658	MCF-7	breast:	n/a	n/a
33	CTCF	chr7:109332801-109332840	MCF-7	breast:	n/a	n/a
34	CTCF	chr7:109333859-109333975	Hela-S3	cervix:	n/a	n/a
35	CTCF	chr7:109256654-109256695	LNCaP	prostate:	n/a	n/a
36	CTCF	chr7:109313795-109313828	GM10248	blood:	n/a	n/a
37	CTCF	chr7:109327987-109328017	Pancreas_OC	pancreas:	n/a	n/a
38	CTCF	chr7:109250577-109250661	GM19240	blood:	n/a	n/a
39	CTCF	chr7:109272060-109272210	HRPEpiC	eye:	n/a	n/a
40	CTCF	chr7:109333860-109334010	SK-N-SH_RA	brain:	n/a	n/a
41	CTCF	chr7:109316250-109316289	MCF-7	breast:	n/a	n/a
42	CTCF	chr7:109308240-109308390	HBMEC	blood vessel:	n/a	n/a
43	CTCF	chr7:109243860-109244010	MCF-7	breast:	n/a	n/a
44	E2F4	chr7:109281514-109281685	MCF10A-Er-Src	breast:	n/a	n/a
45	E2F4	chr7:109322980-109323271	MCF10A-Er-Src	breast:	n/a	chr7:109323192-109323201
46	E2F4	chr7:109249305-109249498	MCF10A-Er-Src	breast:	n/a	n/a
47	E2F4	chr7:109348997-109349054	MCF10A-Er-Src	breast:	n/a	n/a
48	E2F4	chr7:109266388-109266413	MCF10A-Er-Src	breast:	n/a	n/a
49	E2F4	chr7:109262449-109262649	MCF10A-Er-Src	breast:	n/a	n/a
50	E2F4	chr7:109257822-109258237	MCF10A-Er-Src	breast:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:109280498-109280548	Caco-2	colon:	n/a
2	chr7:109280498-109280548	H1-hESC	embryonic stem cell:	embryo
3	chr7:109280498-109280548	Jurkat	blood:	n/a
4	chr7:109280498-109280548	BJ	skin:	n/a
5	chr7:109280498-109280548	HAEpiC	amniotic membrane:	n/a
6	chr7:109280498-109280548	Hela-S3	cervix:	n/a
7	chr7:109280498-109280548	NT2-D1	testis:	n/a
8	chr7:109280498-109280548	GM12878	blood:	n/a
9	chr7:109280498-109280548	SK-N-SH_RA	brain:	n/a
10	chr7:109280498-109280548	HCF	heart:	n/a
11	chr7:109280498-109280548	SK-N-SH	brain:	n/a
12	chr7:109280498-109280548	HCM	heart:	n/a
13	chr7:109280498-109280548	HCPEpiC	choroid plexus:	n/a
14	chr7:109280498-109280548	RPTEC	kidney:	n/a
15	chr7:109280498-109280548	NHBE	bronchial:	n/a
16	chr7:109280498-109280548	A549	lung:	n/a
17	chr7:109280498-109280548	HUVEC	blood vessel:	n/a
18	chr7:109280498-109280548	GM12891	blood:	n/a
19	chr7:109280498-109280548	NH-A	brain:	n/a
20	chr7:109280498-109280548	HEEpiC	esophagus:	n/a
21	chr7:109280498-109280548	HNPCEpiC	eye:	n/a
22	chr7:109280498-109280548	HRE	kidney:	n/a
23	chr7:109280498-109280548	U87	brain:	n/a
24	chr7:109280498-109280548	CMK	blood:	n/a
25	chr7:109280498-109280548	HIPEpiC	eye:	n/a
26	chr7:109280498-109280548	AG04450	lung:	fetal
27	chr7:109280498-109280548	GM19239	blood:	n/a
28	chr7:109280498-109280548	PANC-1	pancreas:	n/a
29	chr7:109280498-109280548	AoSMC	blood vessel:	n/a
30	chr7:109280498-109280548	ovcar-3	ovarian:	n/a
31	chr7:109280498-109280548	K562	blood:	n/a
32	chr7:109280498-109280548	GM06990	blood:	n/a
33	chr7:109280498-109280548	HCT-116	colon:	n/a
34	chr7:109280498-109280548	LNCaP	prostate:	n/a
35	chr7:109280498-109280548	PrEC	prostate:	n/a
36	chr7:109280498-109280548	SAEC	small airway:	n/a
37	chr7:109280498-109280548	SK-N-MC	brain:	n/a
38	chr7:109280498-109280548	AG10803	skin:	n/a
39	chr7:109280498-109280548	NHDF-neo	bronchial:	n/a
40	chr7:109280498-109280548	HEK293	kidney:	embryo
41	chr7:109280498-109280548	HMEC	breast:	n/a
42	chr7:109280498-109280548	HepG2	liver:	n/a
43	chr7:109280498-109280548	GM12892	blood:	n/a
44	chr7:109280498-109280548	AG09319	gingival:	n/a
45	chr7:109280498-109280548	IMR90	lung:	fetal
46	chr7:109280498-109280548	HPAEpiC	pulmonary alveolar:	n/a
47	chr7:109280498-109280548	Hepatocyte	liver:	n/a
48	chr7:109280498-109280548	HRCEpiC	kidney:	n/a
49	chr7:109280498-109280548	HRPEpiC	eye:	n/a
50	chr7:109280498-109280548	ProgFib	skin:	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:109302932..109305473-chr7:109306477..109308301,2	MCF-7	breast:
2	chr7:109347398..109349731-chr7:109349920..109352045,2	K562	blood:
3	chr7:109123447..109124078-chr7:109346229..109346761,2	MCF-7	breast:
4	chr7:109347398..109349731-chr7:109349920..109352045,2	K562	blood:
5	chr7:109302932..109305473-chr7:109306477..109308301,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DNAJB9-5	chr7:109300688-109300946	NONHSAT122753
2	lnc-DNAJB9-4	chr7:109282717-109284286	NONHSAT122754
3	lnc-DNAJB9-4	chr7:109282717-109282873	FPKM1_group_30154_transcript_2
4	lnc-DNAJB9-5	chr7:109300151-109300859	NONHSAT122755
5	lnc-DNAJB9-4	chr7:109281035-109282154	FPKM1_group_30154_transcript_2
6	lnc-DNAJB9-4	chr7:109281035-109282154	NONHSAT122754

Variant related genes	Relation type
ENSG00000230192	TF binding region
ENSG00000234273	TF binding region
ENSG00000230192	CpG island
ENSG00000234273	CpG island

Extended variants
information (count: 2901 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:2901 , 50 per page) page: 1 2 3 4 5 6 7 ... 59

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1721425	chr7:109240101-109240102	Enhancers Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs184091157	chr7:109240105-109240106	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs564085092	chr7:109240153-109240154	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs531098395	chr7:109240154-109240155	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs532484010	chr7:109240173-109240174	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs187841855	chr7:109240215-109240216	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs565762341	chr7:109240252-109240253	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs190926204	chr7:109240298-109240299	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs548639107	chr7:109240299-109240300	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs568742325	chr7:109240315-109240316	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs1721424	chr7:109240337-109240338	Enhancers Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs557549774	chr7:109240338-109240339	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs144206461	chr7:109240363-109240364	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs539569991	chr7:109240364-109240365	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs183185842	chr7:109240405-109240406	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs374230620	chr7:109240427-109240428	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs572917687	chr7:109240470-109240471	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs541843828	chr7:109240495-109240496	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs561479032	chr7:109240509-109240510	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs541217069	chr7:109240554-109240555	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs113052543	chr7:109240562-109240563	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs200598908	chr7:109240566-109240567	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs575503118	chr7:109240639-109240640	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs544142556	chr7:109240710-109240711	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs114000982	chr7:109240734-109240735	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs370549704	chr7:109240749-109240750	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs146532860	chr7:109240752-109240753	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs35312711	chr7:109240759-109240760	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs1464743	chr7:109240787-109240788	Enhancers Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs544799466	chr7:109240818-109240819	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs559408756	chr7:109240934-109240935	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs528510335	chr7:109240937-109240938	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs548576373	chr7:109240961-109240962	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs568332031	chr7:109240977-109240978	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs531260479	chr7:109240978-109240979	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs550971591	chr7:109240982-109240983	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs571092828	chr7:109240984-109240985	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs200637538	chr7:109241001-109241002	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs112631415	chr7:109241002-109241003	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs1721422	chr7:109241003-109241004	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs552490658	chr7:109241034-109241035	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs373365756	chr7:109241043-109241044	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs566574825	chr7:109241049-109241050	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs13242834	chr7:109241068-109241069	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs535162031	chr7:109241099-109241100	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs555356700	chr7:109241226-109241227	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs575103171	chr7:109241237-109241238	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs5029081	chr7:109241269-109241270	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs111712437	chr7:109241301-109241302	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs552478167	chr7:109241308-109241309	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:90)

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
Acute myeloid leukemia	16864856	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
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21785460	CNVD
Chronic myeloid leukemia	21384125	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	21364760	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	17053054	CNVD
Prostate cancer	16573809	CNVD
Medulloblastoma	16783165	CNVD
Melanoma	17363583	CNVD
Myelofibrosis	22110671	CNVD
Squamous cell cancer	20885788	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Breast cancer	16397240	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
Autism	19401682	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	19546859	CNVD
Schizophrenia	19546859	CNVD
Tourette syndrome	19546859	CNVD
Melanoma	19188590	CNVD
small cell lung cancer	20016488	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
early-passage human iPS cells	21368824	CNVD
Cancer	21272361	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:131 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:109237400-109240400	Weak transcription	HUES64 Cell Line	embryonic stem cell
2	chr7:109238400-109240600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
3	chr7:109238600-109240600	Weak transcription	HUES48 Cell Line	embryonic stem cell
4	chr7:109238600-109241400	Enhancers	iPS-15b Cell Line	embryonic stem cell
5	chr7:109239200-109241400	Enhancers	iPS-18 Cell Line	embryonic stem cell
6	chr7:109239600-109240800	Enhancers	ES-I3 Cell Line	embryonic stem cell
7	chr7:109239600-109241200	Enhancers	Dnd41	blood
8	chr7:109240000-109240600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
9	chr7:109240000-109243800	Weak transcription	H9 Cell Line	embryonic stem cell
10	chr7:109240000-109245000	Weak transcription	HUES6 Cell Line	embryonic stem cell
11	chr7:109240400-109241200	Enhancers	HUES64 Cell Line	embryonic stem cell
12	chr7:109240600-109240800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
13	chr7:109240600-109241000	Enhancers	HUES48 Cell Line	embryonic stem cell
14	chr7:109240600-109241000	Enhancers	iPS-20b Cell Line	embryonic stem cell
15	chr7:109240800-109244000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
16	chr7:109240800-109261800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
17	chr7:109241000-109242800	Weak transcription	HUES48 Cell Line	embryonic stem cell
18	chr7:109241400-109241800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
19	chr7:109241400-109241800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
20	chr7:109241800-109244400	Enhancers	iPS-18 Cell Line	embryonic stem cell
21	chr7:109241800-109244600	Enhancers	iPS-15b Cell Line	embryonic stem cell
22	chr7:109242800-109243000	Enhancers	HUES48 Cell Line	embryonic stem cell
23	chr7:109243000-109243600	Weak transcription	HUES48 Cell Line	embryonic stem cell
24	chr7:109243600-109243800	Enhancers	HUES48 Cell Line	embryonic stem cell
25	chr7:109244000-109244200	Genic enhancers	ES-I3 Cell Line	embryonic stem cell
26	chr7:109244200-109244800	Strong transcription	ES-I3 Cell Line	embryonic stem cell
27	chr7:109244800-109250400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
28	chr7:109250200-109253000	Enhancers	Dnd41	blood
29	chr7:109250400-109252600	Enhancers	ES-I3 Cell Line	embryonic stem cell
30	chr7:109251000-109252000	Enhancers	iPS-15b Cell Line	embryonic stem cell
31	chr7:109251200-109252000	Enhancers	HUES64 Cell Line	embryonic stem cell
32	chr7:109251600-109252200	Enhancers	iPS-18 Cell Line	embryonic stem cell
33	chr7:109260800-109261200	Enhancers	Fetal Lung	lung
34	chr7:109263600-109264200	Enhancers	Dnd41	blood
35	chr7:109264000-109265800	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
36	chr7:109264400-109264800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
37	chr7:109264400-109265000	Enhancers	HMEC	breast
38	chr7:109264600-109265000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
39	chr7:109264600-109265000	Enhancers	H9 Cell Line	embryonic stem cell
40	chr7:109265000-109265600	Weak transcription	H9 Cell Line	embryonic stem cell
41	chr7:109265000-109267000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr7:109265600-109266000	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
43	chr7:109265600-109266000	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
44	chr7:109272000-109273600	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
45	chr7:109272200-109274000	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
46	chr7:109273600-109276000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
47	chr7:109275400-109275600	Enhancers	Fetal Lung	lung
48	chr7:109275600-109277000	Weak transcription	Fetal Lung	lung
49	chr7:109276000-109276200	Enhancers	ES-I3 Cell Line	embryonic stem cell
50	chr7:109276000-109276200	Enhancers	iPS-15b Cell Line	embryonic stem cell

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