Variant report

Variant	nsv889240
Chromosome Location	chr7:136972027-137038092
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:439)
CpG islands
(count:1162)
Chromatin interactive
region (count:6)
LncRNA
region (count:10)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:439 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr7:136992921-136992933	H1-hESC	embryonic stem cell:	n/a	n/a
2	BRCA1	chr7:137028122-137028571	H1-hESC	embryonic stem cell:	n/a	n/a
3	CEBPB	chr7:137023920-137024145	IMR90	lung:	n/a	n/a
4	CEBPB	chr7:137023871-137024074	HepG2	liver:	n/a	n/a
5	CEBPB	chr7:137020635-137020980	IMR90	lung:	n/a	n/a
6	CEBPB	chr7:137020688-137020924	Hela-S3	cervix:	n/a	n/a
7	CEBPB	chr7:137023922-137024163	A549	lung:	n/a	n/a
8	CHD2	chr7:137028267-137028479	H1-hESC	embryonic stem cell:	n/a	n/a
9	CTBP2	chr7:137028095-137028618	H1-hESC	embryonic stem cell:	n/a	n/a
10	CTCF	chr7:136989480-136989630	HVMF	connective:	n/a	n/a
11	CTCF	chr7:136972500-136972650	HMF	breast:	n/a	n/a
12	CTCF	chr7:137022960-137023110	NHDF-neo	bronchial:	n/a	n/a
13	CTCF	chr7:137022767-137022908	MCF-7	breast:	n/a	chr7:137022848-137022866 chr7:137022843-137022864
14	CTCF	chr7:137022760-137022910	HMEC	breast:	n/a	chr7:137022848-137022866 chr7:137022843-137022864
15	CTCF	chr7:137022619-137022949	H1-hESC	embryonic stem cell:	n/a	chr7:137022848-137022866 chr7:137022843-137022864
16	CTCF	chr7:136972404-136972761	IMR90	lung:	n/a	n/a
17	CTCF	chr7:137022800-137022950	HCFaa	heart:	n/a	chr7:137022848-137022866 chr7:137022843-137022864
18	CTCF	chr7:137022808-137022866	GM12892	blood:	n/a	chr7:137022848-137022866 chr7:137022843-137022864
19	CTCF	chr7:137022791-137022920	GM13977	blood:	n/a	chr7:137022848-137022866 chr7:137022843-137022864
20	CTCF	chr7:136972520-136972670	HFF-Myc	foreskin:	n/a	n/a
21	CTCF	chr7:136972520-136972670	HBMEC	blood vessel:	n/a	n/a
22	CTCF	chr7:136989420-136989570	HCM	heart:	n/a	n/a
23	CTCF	chr7:136972580-136972730	HEEpiC	esophagus:	n/a	n/a
24	CTCF	chr7:137022740-137022890	GM12871	blood:	n/a	chr7:137022848-137022866 chr7:137022843-137022864
25	CTCF	chr7:137022780-137022930	SAEC	small airway:	n/a	chr7:137022848-137022866 chr7:137022843-137022864
26	CTCF	chr7:136972600-136972750	GM12875	blood:	n/a	n/a
27	CTCF	chr7:136989440-136989590	BE2_C	brain:	n/a	n/a
28	CTCF	chr7:137022800-137022950	NHLF	lung:	n/a	chr7:137022848-137022866 chr7:137022843-137022864
29	CTCF	chr7:136972520-136972670	HRE	kidney:	n/a	n/a
30	CTCF	chr7:137022760-137022910	GM12875	blood:	n/a	chr7:137022848-137022866 chr7:137022843-137022864
31	CTCF	chr7:137022720-137022870	BJ	skin:	n/a	chr7:137022848-137022866 chr7:137022843-137022864
32	CTCF	chr7:137022774-137022905	GM19238	blood:	n/a	chr7:137022848-137022866 chr7:137022843-137022864
33	CTCF	chr7:137022760-137022910	RPTEC	kidney:	n/a	chr7:137022848-137022866 chr7:137022843-137022864
34	CTCF	chr7:136972530-136972628	Hela-S3	cervix:	n/a	n/a
35	CTCF	chr7:136989560-136989710	HCFaa	heart:	n/a	n/a
36	CTCF	chr7:137022820-137022970	HRE	kidney:	n/a	chr7:137022848-137022866 chr7:137022843-137022864
37	CTCF	chr7:136972480-136972630	RPTEC	kidney:	n/a	n/a
38	CTCF	chr7:136972560-136972710	SK-N-SH_RA	brain:	n/a	n/a
39	CTCF	chr7:137022740-137022890	A549	lung:	n/a	chr7:137022848-137022866 chr7:137022843-137022864
40	CTCF	chr7:137022780-137022930	HA-sp	spinal cord:	n/a	chr7:137022848-137022866 chr7:137022843-137022864
41	CTCF	chr7:137028260-137028410	AG04450	lung:	n/a	n/a
42	CTCF	chr7:137022820-137022970	AG09319	gingival:	n/a	chr7:137022848-137022866 chr7:137022843-137022864
43	CTCF	chr7:136972460-136972610	GM12865	blood:	n/a	n/a
44	CTCF	chr7:137028480-137028630	SK-N-SH_RA	brain:	n/a	n/a
45	CTCF	chr7:136972540-136972690	AG09309	skin:	n/a	n/a
46	CTCF	chr7:137022856-137022895	GM10266	blood:	n/a	n/a
47	CTCF	chr7:136972529-136972658	LNCaP	prostate:	n/a	n/a
48	CTCF	chr7:136972568-136972617	Pancreas_OC	pancreas:	n/a	n/a
49	CTCF	chr7:137022740-137022890	SK-N-SH_RA	brain:	n/a	chr7:137022848-137022866 chr7:137022843-137022864
50	CTCF	chr7:137022820-137022970	AG04450	lung:	n/a	chr7:137022848-137022866 chr7:137022843-137022864

(count:1162 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:137002261-137002311	HCM	heart:	n/a
2	chr7:136973838-136973888	GM06990	blood:	n/a
3	chr7:137028165-137028215	HRE	kidney:	n/a
4	chr7:137002261-137002311	HCM	heart:	n/a
5	chr7:136973838-136973888	GM06990	blood:	n/a
6	chr7:137028165-137028215	HRE	kidney:	n/a
7	chr7:137003665-137003715	HIPEpiC	eye:	n/a
8	chr7:137028546-137028596	Hela-S3	cervix:	n/a
9	chr7:137027135-137027185	PrEC	prostate:	n/a
10	chr7:137029097-137029147	PANC-1	pancreas:	n/a
11	chr7:137028604-137028654	CMK	blood:	n/a
12	chr7:137002261-137002311	HL-60	blood:	n/a
13	chr7:137028546-137028596	GM12892	blood:	n/a
14	chr7:137027135-137027185	HCM	heart:	n/a
15	chr7:137011196-137011246	SK-N-SH	brain:	n/a
16	chr7:137003665-137003715	HMEC	breast:	n/a
17	chr7:137002261-137002311	A549	lung:	n/a
18	chr7:137029097-137029147	PrEC	prostate:	n/a
19	chr7:137028546-137028596	HAEpiC	amniotic membrane:	n/a
20	chr7:137028389-137028439	Caco-2	colon:	n/a
21	chr7:137029097-137029147	ovcar-3	ovarian:	n/a
22	chr7:137028617-137028667	HL-60	blood:	n/a
23	chr7:137028972-137029022	BE2_C	brain:	n/a
24	chr7:137028604-137028654	AG04449	skin:	fetal
25	chr7:137013465-137013515	HCT-116	colon:	n/a
26	chr7:137028389-137028439	Jurkat	blood:	n/a
27	chr7:137028389-137028439	GM12878	blood:	n/a
28	chr7:137028198-137028248	Jurkat	blood:	n/a
29	chr7:136973838-136973888	NHBE	bronchial:	n/a
30	chr7:137002261-137002311	Hepatocyte	liver:	n/a
31	chr7:137028165-137028215	ovcar-3	ovarian:	n/a
32	chr7:137027135-137027185	HRE	kidney:	n/a
33	chr7:137028442-137028492	PANC-1	pancreas:	n/a
34	chr7:137028165-137028215	T-47D	breast:	n/a
35	chr7:137032114-137032164	ProgFib	skin:	n/a
36	chr7:137028546-137028596	BJ	skin:	n/a
37	chr7:136989898-136989948	HEK293	kidney:	embryo
38	chr7:137011196-137011246	HAEpiC	amniotic membrane:	n/a
39	chr7:137028198-137028248	Hela-S3	cervix:	n/a
40	chr7:137028442-137028492	HAEpiC	amniotic membrane:	n/a
41	chr7:136973838-136973888	HIPEpiC	eye:	n/a
42	chr7:137032114-137032164	NH-A	brain:	n/a
43	chr7:137028604-137028654	RPTEC	kidney:	n/a
44	chr7:137028410-137028460	PrEC	prostate:	n/a
45	chr7:136989898-136989948	Caco-2	colon:	n/a
46	chr7:137028389-137028439	AG09319	gingival:	n/a
47	chr7:137028972-137029022	Hepatocyte	liver:	n/a
48	chr7:137028617-137028667	HCPEpiC	choroid plexus:	n/a
49	chr7:137002261-137002311	HUVEC	blood vessel:	n/a
50	chr7:137032114-137032164	LNCaP	prostate:	n/a

(count:6 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:137026451..137029166-chr7:137034024..137036129,2	K562	blood:
2	chr7:136983518..136985110-chr7:136986061..136988614,2	MCF-7	breast:
3	chr7:136983518..136985110-chr7:136986061..136988614,2	MCF-7	breast:
4	chr7:136853636..136854568-chr7:137022322..137023760,5	MCF-7	breast:
5	chr7:136853684..136854424-chr7:137022605..137023178,2	MCF-7	breast:
6	chr12:62807018..62807608-chr7:136989360..136989935,2	MCF-7	breast:

(count:10 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CHRM2-1	chr7:137010132-137011700	ENSG00000231114
2	lnc-PTN-1	chr7:137037223-137037354	XLOC_006620
3	lnc-CHRM2-1	chr7:137003339-137003604	ENSG00000231114
4	lnc-PTN-1	chr7:137035099-137035212	NONHSAT123582
5	lnc-PTN-1	chr7:137035115-137035212	ENSG00000228031.2
6	lnc-PTN-1	chr7:137035115-137035216	XLOC_006620
7	lnc-PTN-1	chr7:137037223-137037354	NONHSAT123582
8	lnc-PTN-1	chr7:137029676-137029876	ENSG00000228031.2
9	lnc-PTN-1	chr7:137029676-137029876	XLOC_006620
10	lnc-PTN-1	chr7:137037223-137037354	ENSG00000228031.2

No data

Variant related genes	Relation type
PTN	TF binding region
ENSG00000231114	TF binding region
ENSG00000202023	TF binding region
PTN	CpG island
ENSG00000231114	CpG island
ENSG00000202023	CpG island
ENSG00000105894	chromatin interactions
NSF	miRNA target sites
ADARB1	miRNA target sites
SEC61A1	miRNA target sites

Extended variants
information (count: 2419 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:2419 , 50 per page) page: 1 2 3 4 5 6 7 ... 49

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11765480	chr7:136972027-136972028	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs561628207	chr7:136972029-136972030	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs373475660	chr7:136972100-136972101	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs530509119	chr7:136972116-136972117	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs539044342	chr7:136972121-136972122	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs188715173	chr7:136972145-136972146	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs368917676	chr7:136972186-136972187	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs60406979	chr7:136972199-136972200	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs397798349	chr7:136972209-136972210	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs17661392	chr7:136972378-136972379	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
11	rs181104057	chr7:136972403-136972404	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs546442376	chr7:136972455-136972456	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs186176592	chr7:136972521-136972522	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs528518184	chr7:136972527-136972528	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs137900432	chr7:136972564-136972565	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs562406916	chr7:136972587-136972588	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs369936094	chr7:136972588-136972589	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs190641343	chr7:136972673-136972674	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs537042704	chr7:136972678-136972679	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs557660604	chr7:136972690-136972691	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs571025358	chr7:136972721-136972722	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs540047724	chr7:136972740-136972741	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs182766280	chr7:136972741-136972742	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs572986278	chr7:136972771-136972772	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs76370532	chr7:136972794-136972795	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs555498487	chr7:136972809-136972810	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs575341813	chr7:136972884-136972885	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs187320587	chr7:136972938-136972939	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs564420430	chr7:136972955-136972956	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs6979228	chr7:136972966-136972967	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs540425727	chr7:136972969-136972970	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs62487109	chr7:136972986-136972987	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs190877630	chr7:136972995-136972996	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs183013380	chr7:136973013-136973014	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs376336006	chr7:136973021-136973022	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs6961235	chr7:136973027-136973028	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs187224594	chr7:136973032-136973033	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs550674012	chr7:136973050-136973051	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs10235309	chr7:136973083-136973084	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs539706909	chr7:136973099-136973100	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs56352664	chr7:136973112-136973113	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs6979268	chr7:136973140-136973141	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs530076777	chr7:136973156-136973157	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs371525820	chr7:136973163-136973164	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs547960990	chr7:136973166-136973167	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs78428127	chr7:136973189-136973190	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs368487181	chr7:136973215-136973216	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs562766337	chr7:136973223-136973224	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs575375672	chr7:136973248-136973249	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs191685189	chr7:136973260-136973261	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:87)

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
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
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	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
Adenocarcinoma	21044232	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Melanoma	19188590	CNVD
Glioblastoma multiforme	18628472	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Malignant melanoma	17260012	CNVD
Coffin-Siris syndrome	21572526	CNVD
Papillary thyroid carcinoma	21436994	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Hodgkin''s lymphoma	18179710	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	21509527	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Low-grade fibromyxoid sarcoma	21536545	CNVD
Breast cancer	16272173	CNVD
Myxofibrosarcoma	16751306	CNVD
Stuttering	21108403	CNVD
Breast cancer	17603634	CNVD
Urothelial carcinoma	18382360	CNVD
Neuroticism	17667963	CNVD
Myelodysplastic syndrome	17634407	CNVD
Acute myeloid leukemia	17237825	CNVD
Esophageal cancer	21851588	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Pancreatic cancer	17952125	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	21990379	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:1027 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:136938200-136980600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
2	chr7:136961400-136973600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
3	chr7:136961400-136980600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr7:136968000-136973600	Enhancers	Cortex derived primary cultured neurospheres	brain
5	chr7:136968600-136989600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
6	chr7:136969600-136973800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
7	chr7:136969600-136974200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr7:136970600-136972800	Enhancers	Brain Hippocampus Middle	brain
9	chr7:136971600-136972200	Enhancers	Brain Cingulate Gyrus	brain
10	chr7:136971600-136972200	Enhancers	Brain Inferior Temporal Lobe	brain
11	chr7:136971800-136972200	Enhancers	Brain Angular Gyrus	brain
12	chr7:136972000-136972200	Enhancers	Fetal Stomach	stomach
13	chr7:136972000-136978400	Weak transcription	Brain Substantia Nigra	brain
14	chr7:136972200-136978000	Weak transcription	Brain Cingulate Gyrus	brain
15	chr7:136972200-136979400	Weak transcription	Brain Angular Gyrus	brain
16	chr7:136972200-136990400	Weak transcription	Fetal Stomach	stomach
17	chr7:136972600-136973800	Enhancers	iPS-18 Cell Line	embryonic stem cell
18	chr7:136972600-136974000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
19	chr7:136972800-136973800	Enhancers	HUES48 Cell Line	embryonic stem cell
20	chr7:136972800-136978800	Weak transcription	Brain Hippocampus Middle	brain
21	chr7:136973000-136976200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
22	chr7:136973600-136973800	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
23	chr7:136973600-136974600	Enhancers	iPS-15b Cell Line	embryonic stem cell
24	chr7:136973600-136974800	Enhancers	HUES64 Cell Line	embryonic stem cell
25	chr7:136973600-136975200	Genic enhancers	Cortex derived primary cultured neurospheres	brain
26	chr7:136973800-136974000	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
27	chr7:136973800-136974000	Genic enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
28	chr7:136973800-136974200	Active TSS	iPS-20b Cell Line	embryonic stem cell
29	chr7:136973800-136974400	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
30	chr7:136973800-136974600	Enhancers	HUES6 Cell Line	embryonic stem cell
31	chr7:136973800-136974600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
32	chr7:136974000-136974200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
33	chr7:136974000-136974200	Enhancers	iPS-18 Cell Line	embryonic stem cell
34	chr7:136974000-136974600	Enhancers	H1 Cell Line	embryonic stem cell
35	chr7:136974000-136974600	Enhancers	H9 Cell Line	embryonic stem cell
36	chr7:136974000-136974600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
37	chr7:136974000-136977200	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
38	chr7:136974200-136974400	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
39	chr7:136974200-136974400	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
40	chr7:136974200-136974800	Enhancers	ES-I3 Cell Line	embryonic stem cell
41	chr7:136974200-136975200	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr7:136974400-136974600	Enhancers	HUES48 Cell Line	embryonic stem cell
43	chr7:136974400-136974600	Enhancers	iPS-18 Cell Line	embryonic stem cell
44	chr7:136974400-136974800	Enhancers	iPS-20b Cell Line	embryonic stem cell
45	chr7:136974600-136974800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
46	chr7:136974600-136982600	Weak transcription	H1 Cell Line	embryonic stem cell
47	chr7:136974600-136983600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
48	chr7:136974800-136975000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr7:136974800-136975000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
50	chr7:136974800-136975200	ZNF genes & repeats	iPS-18 Cell Line	embryonic stem cell

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