Variant report

Variant	nsv917169
Chromosome Location	chr7:146581546-146663236
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	CEBPB	chr7:146650551-146650805	IMR90	lung:	n/a	chr7:146650646-146650655 chr7:146650646-146650655
2	CEBPB	chr7:146582398-146582629	ECC-1	luminal epithelium:	n/a	chr7:146582542-146582553
3	CEBPB	chr7:146653286-146653563	HepG2	liver:	n/a	chr7:146653389-146653398 chr7:146653389-146653398 chr7:146653387-146653400 chr7:146653389-146653398
4	CEBPB	chr7:146658691-146659162	ECC-1	luminal epithelium:	n/a	n/a
5	CEBPB	chr7:146631945-146632234	HepG2	liver:	n/a	n/a
6	CEBPB	chr7:146653225-146653552	A549	lung:	n/a	chr7:146653389-146653398 chr7:146653389-146653398 chr7:146653387-146653400 chr7:146653389-146653398
7	CEBPB	chr7:146645855-146646062	A549	lung:	n/a	n/a
8	CEBPB	chr7:146631955-146632230	A549	lung:	n/a	n/a
9	CEBPB	chr7:146650625-146650798	K562	blood:	n/a	chr7:146650646-146650655 chr7:146650646-146650655
10	CREB1	chr7:146658679-146659194	ECC-1	luminal epithelium:	n/a	n/a
11	CTCF	chr7:146658180-146658330	NB4	blood:	n/a	chr7:146658279-146658288
12	CTCF	chr7:146658283-146658413	MCF-7	breast:	n/a	chr7:146658320-146658341 chr7:146658325-146658343
13	CTCF	chr7:146658313-146658318	Medullo	brain:	n/a	n/a
14	CTCF	chr7:146658200-146658350	AG09319	gingival:	n/a	chr7:146658320-146658341 chr7:146658325-146658343 chr7:146658279-146658288
15	CTCF	chr7:146658210-146658474	Gliobla	brain:	n/a	chr7:146658320-146658341 chr7:146658325-146658343 chr7:146658279-146658288
16	CTCF	chr7:146658790-146658873	Gliobla	brain:	n/a	n/a
17	CTCF	chr7:146658237-146658455	H1-hESC	embryonic stem cell:	n/a	chr7:146658320-146658341 chr7:146658325-146658343 chr7:146658279-146658288
18	CTCF	chr7:146658740-146658890	HEK293	kidney:	n/a	n/a
19	CTCF	chr7:146658220-146658370	BE2_C	brain:	n/a	chr7:146658320-146658341 chr7:146658325-146658343 chr7:146658279-146658288
20	CTCF	chr7:146592560-146592710	HL-60	blood:	n/a	n/a
21	CTCF	chr7:146658200-146658350	AG04449	skin:	n/a	chr7:146658320-146658341 chr7:146658325-146658343 chr7:146658279-146658288
22	CTCF	chr7:146658220-146658370	HCPEpiC	choroid plexus:	n/a	chr7:146658320-146658341 chr7:146658325-146658343 chr7:146658279-146658288
23	CTCF	chr7:146658200-146658350	SK-N-SH_RA	brain:	n/a	chr7:146658320-146658341 chr7:146658325-146658343 chr7:146658279-146658288
24	CTCF	chr7:146658290-146658408	MCF-7	breast:	n/a	chr7:146658320-146658341 chr7:146658325-146658343
25	CTCF	chr7:146648086-146648177	LNCaP	prostate:	n/a	n/a
26	CTCF	chr7:146658740-146658890	HBMEC	blood vessel:	n/a	n/a
27	CTCF	chr7:146658082-146658536	MCF-7	breast:	n/a	chr7:146658320-146658341 chr7:146658325-146658343 chr7:146658279-146658288
28	CTCF	chr7:146658180-146658330	AG10803	skin:	n/a	chr7:146658279-146658288
29	CTCF	chr7:146658240-146658390	HEK293	kidney:	n/a	chr7:146658320-146658341 chr7:146658325-146658343 chr7:146658279-146658288
30	CTCF	chr7:146588033-146588050	GM13977	blood:	n/a	n/a
31	CTCF	chr7:146658720-146658870	HCFaa	heart:	n/a	n/a
32	CTCF	chr7:146657184-146657206	GM10266	blood:	n/a	n/a
33	CTCF	chr7:146658220-146658370	HRE	kidney:	n/a	chr7:146658320-146658341 chr7:146658325-146658343 chr7:146658279-146658288
34	CTCF	chr7:146658342-146658355	HepG2	liver:	n/a	n/a
35	CTCF	chr7:146658097-146658532	H1-hESC	embryonic stem cell:	n/a	chr7:146658320-146658341 chr7:146658325-146658343 chr7:146658279-146658288
36	CTCF	chr7:146658200-146658350	HBMEC	blood vessel:	n/a	chr7:146658320-146658341 chr7:146658325-146658343 chr7:146658279-146658288
37	CTCF	chr7:146658260-146658410	HEK293	kidney:	n/a	chr7:146658320-146658341 chr7:146658325-146658343 chr7:146658279-146658288
38	CTCF	chr7:146658075-146658460	H1-hESC	embryonic stem cell:	n/a	chr7:146658320-146658341 chr7:146658325-146658343 chr7:146658279-146658288
39	CTCF	chr7:146658660-146658810	HAc	cerebellar:	n/a	n/a
40	CTCF	chr7:146658220-146658370	HPF	lung:	n/a	chr7:146658320-146658341 chr7:146658325-146658343 chr7:146658279-146658288
41	CTCF	chr7:146662220-146662370	SK-N-SH_RA	brain:	n/a	n/a
42	CTCF	chr7:146658260-146658410	WERI-Rb-1	eye:	n/a	chr7:146658320-146658341 chr7:146658325-146658343 chr7:146658279-146658288
43	CTCF	chr7:146658303-146658385	MCF-7	breast:	n/a	chr7:146658320-146658341 chr7:146658325-146658343
44	CTCF	chr7:146658240-146658390	HRPEpiC	eye:	n/a	chr7:146658320-146658341 chr7:146658325-146658343 chr7:146658279-146658288
45	CTCF	chr7:146658200-146658350	MCF-7	breast:	n/a	chr7:146658320-146658341 chr7:146658325-146658343 chr7:146658279-146658288
46	CTCF	chr7:146658266-146658433	MCF-7	breast:	n/a	chr7:146658320-146658341 chr7:146658325-146658343 chr7:146658279-146658288
47	CTCF	chr7:146658240-146658390	HRE	kidney:	n/a	chr7:146658320-146658341 chr7:146658325-146658343 chr7:146658279-146658288
48	CTCF	chr7:146658240-146658390	BE2_C	brain:	n/a	chr7:146658320-146658341 chr7:146658325-146658343 chr7:146658279-146658288
49	CTCF	chr7:146658720-146658870	AG10803	skin:	n/a	n/a
50	CTCF	chr7:146658220-146658370	Caco-2	colon:	n/a	chr7:146658320-146658341 chr7:146658325-146658343 chr7:146658279-146658288

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:146603166-146603216	CMK	blood:	n/a
2	chr7:146603166-146603216	CMK	blood:	n/a
3	chr7:146603166-146603216	HRCEpiC	kidney:	n/a
4	chr7:146635353-146635403	Caco-2	colon:	n/a
5	chr7:146603166-146603216	PrEC	prostate:	n/a
6	chr7:146603166-146603216	SKMC	muscle:	n/a
7	chr7:146603166-146603216	NT2-D1	testis:	n/a
8	chr7:146603166-146603216	NB4	blood:	n/a
9	chr7:146635353-146635403	AoSMC	blood vessel:	n/a
10	chr7:146635353-146635403	SAEC	small airway:	n/a
11	chr7:146635353-146635403	NT2-D1	testis:	n/a
12	chr7:146603166-146603216	AoSMC	blood vessel:	n/a
13	chr7:146603166-146603216	GM12891	blood:	n/a
14	chr7:146635353-146635403	SK-N-SH_RA	brain:	n/a
15	chr7:146603166-146603216	BJ	skin:	n/a
16	chr7:146635353-146635403	GM12891	blood:	n/a
17	chr7:146635353-146635403	Hela-S3	cervix:	n/a
18	chr7:146603166-146603216	Hepatocyte	liver:	n/a
19	chr7:146603166-146603216	ovcar-3	ovarian:	n/a
20	chr7:146635353-146635403	HCF	heart:	n/a
21	chr7:146635353-146635403	PFSK-1	brain:	n/a
22	chr7:146603166-146603216	HRPEpiC	eye:	n/a
23	chr7:146635353-146635403	MCF-7	breast:	n/a
24	chr7:146635353-146635403	HMEC	breast:	n/a
25	chr7:146635353-146635403	NB4	blood:	n/a
26	chr7:146635353-146635403	BJ	skin:	n/a
27	chr7:146603166-146603216	T-47D	breast:	n/a
28	chr7:146635353-146635403	SK-N-MC	brain:	n/a
29	chr7:146635353-146635403	HCT-116	colon:	n/a
30	chr7:146635353-146635403	U87	brain:	n/a
31	chr7:146603166-146603216	NH-A	brain:	n/a
32	chr7:146635353-146635403	NH-A	brain:	n/a
33	chr7:146603166-146603216	SAEC	small airway:	n/a
34	chr7:146635353-146635403	PANC-1	pancreas:	n/a
35	chr7:146603166-146603216	A549	lung:	n/a
36	chr7:146635353-146635403	HL-60	blood:	n/a
37	chr7:146635353-146635403	GM12892	blood:	n/a
38	chr7:146603166-146603216	GM06990	blood:	n/a
39	chr7:146603166-146603216	LNCaP	prostate:	n/a
40	chr7:146635353-146635403	IMR90	lung:	fetal
41	chr7:146603166-146603216	HL-60	blood:	n/a
42	chr7:146635353-146635403	HUVEC	blood vessel:	n/a
43	chr7:146635353-146635403	SK-N-SH	brain:	n/a
44	chr7:146603166-146603216	PFSK-1	brain:	n/a
45	chr7:146603166-146603216	AG04450	lung:	fetal
46	chr7:146635353-146635403	HRCEpiC	kidney:	n/a
47	chr7:146603166-146603216	SK-N-MC	brain:	n/a
48	chr7:146635353-146635403	AG04449	skin:	fetal
49	chr7:146603166-146603216	Hela-S3	cervix:	n/a
50	chr7:146603166-146603216	PANC-1	pancreas:	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:146651547..146653225-chr7:146656495..146658548,2	K562	blood:
2	chr7:146657758..146660161-chr7:146662601..146665251,2	K562	blood:
3	chr7:146651547..146653225-chr7:146656495..146658548,2	K562	blood:
4	chr7:146657758..146660161-chr7:146662601..146665251,2	K562	blood:
5	chr7:146570862..146573024-chr7:146579800..146582486,2	K562	blood:

Variant related genes	Relation type
ENSG00000221766	TF binding region
ENSG00000221766	CpG island

Extended variants
information (count: 1238 )
Associated
traits (count: 99 )

Variant overlapped rSNPs/rCNVs (count:1238 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs113651664	chr7:146582820-146582821	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs180917911	chr7:146582821-146582822	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs187041834	chr7:146582824-146582825	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs138496932	chr7:146582860-146582861	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs559045043	chr7:146582908-146582909	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs141937474	chr7:146582922-146582923	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs150326950	chr7:146582923-146582924	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs565876218	chr7:146582941-146582942	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs192381236	chr7:146582971-146582972	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs10244873	chr7:146582979-146582980	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs182807085	chr7:146582980-146582981	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs562533023	chr7:146582982-146582983	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs138749268	chr7:146583012-146583013	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs531420890	chr7:146583019-146583020	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs574541854	chr7:146583021-146583022	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs140625217	chr7:146583056-146583057	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs372983758	chr7:146583057-146583058	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs57709159	chr7:146583059-146583060	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs548434185	chr7:146583065-146583066	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs71165046	chr7:146583066-146583067	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs73742604	chr7:146583067-146583068	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs186000850	chr7:146583102-146583103	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs190058601	chr7:146583115-146583116	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs371801791	chr7:146583147-146583148	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs137966281	chr7:146583256-146583257	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs547632164	chr7:146583286-146583287	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs570764232	chr7:146583311-146583312	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs539421873	chr7:146583342-146583343	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs540829819	chr7:146583350-146583351	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs201236765	chr7:146583379-146583380	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs74274752	chr7:146583380-146583381	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs569841924	chr7:146583410-146583411	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs535548915	chr7:146583414-146583415	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs541530112	chr7:146583430-146583431	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs376663755	chr7:146583532-146583533	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs187021622	chr7:146583545-146583546	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs192178076	chr7:146583584-146583585	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs535009507	chr7:146583585-146583586	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs536445004	chr7:146583589-146583590	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs563428852	chr7:146583627-146583628	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs75105018	chr7:146583643-146583644	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs576777485	chr7:146583646-146583647	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs398086238	chr7:146583648-146583649	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs554471791	chr7:146583655-146583656	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs367767464	chr7:146583662-146583663	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs556174055	chr7:146583678-146583679	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs576251702	chr7:146583715-146583716	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs182924186	chr7:146583732-146583733	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs115494965	chr7:146583757-146583758	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs370175521	chr7:146583776-146583777	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:99)

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
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
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
lymphocytic leukemia	21291569	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16573809	CNVD
Medulloblastoma	16783165	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Glioblastoma multiforme	18628472	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Papillary thyroid carcinoma	21436994	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Hodgkin''s lymphoma	18179710	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	16272173	CNVD
Myxofibrosarcoma	16751306	CNVD
Stuttering	21108403	CNVD
Breast cancer	17603634	CNVD
Urothelial carcinoma	18382360	CNVD
Myelodysplastic syndrome	17634407	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Multiple myeloma	16461302	CNVD
Neuroblastoma	18923191	CNVD
Breast cancer	17133270	CNVD
Schizophrenia	17646849	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Myelofibrosis	22110671	CNVD
Heart disease	21282601	CNVD
Lung adenocarcinoma	17086460	CNVD
Gastric adenocarcinoma	19115996	CNVD
Pancreatitis	21956041	CNVD
Acute myeloid leukemia	16864856	CNVD
Gastric cancer	16891809	CNVD
Lung cancer	17086460	CNVD
Autism	19546859	CNVD
Schizophrenia	19546859	CNVD
Tourette syndrome	19546859	CNVD
Cancer	20164920	CNVD
Pancreatic cancer	17952125	CNVD
Autism	20808228	CNVD
Schizophrenia	20838587	CNVD
Schizophrenia	20718829	CNVD
Neuropsychiatric disorder	21827697	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD
Breast cancer	21509527	CNVD
Autism	20964600	CNVD
Epilepsy	17646849	CNVD
Mental retardation	19896112	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Bipolar disorder	19114987	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:84 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:146582800-146584400	Enhancers	Fetal Brain Male	brain
2	chr7:146587000-146587600	Enhancers	Pancreatic Islets	Pancreatic Islet
3	chr7:146589000-146589400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
4	chr7:146589200-146589600	Enhancers	HUES6 Cell Line	embryonic stem cell
5	chr7:146589400-146589800	Enhancers	ES-I3 Cell Line	embryonic stem cell
6	chr7:146602200-146602800	Active TSS	ES-WA7 Cell Line	embryonic stem cell
7	chr7:146602600-146602800	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
8	chr7:146602800-146603000	Active TSS	ES-I3 Cell Line	embryonic stem cell
9	chr7:146614000-146615400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr7:146616400-146617400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr7:146616800-146617400	Enhancers	Ovary	ovary
12	chr7:146617400-146620200	Weak transcription	Ovary	ovary
13	chr7:146617800-146618200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
14	chr7:146618200-146619600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
15	chr7:146618800-146619000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
16	chr7:146619000-146620200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
17	chr7:146619600-146620000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
18	chr7:146620000-146620400	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
19	chr7:146620200-146620600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
20	chr7:146620200-146620800	Enhancers	Ovary	ovary
21	chr7:146620400-146620600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
22	chr7:146620800-146621200	Weak transcription	Ovary	ovary
23	chr7:146621200-146621400	Enhancers	Ovary	ovary
24	chr7:146621400-146622800	Weak transcription	Ovary	ovary
25	chr7:146622800-146623200	Enhancers	Ovary	ovary
26	chr7:146622800-146623800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr7:146623800-146624800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr7:146624800-146625800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr7:146631800-146632200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr7:146634400-146635000	Enhancers	Fetal Intestine Large	intestine
31	chr7:146645200-146647200	Enhancers	Primary hematopoietic stem cells short term culture	blood
32	chr7:146645600-146646000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
33	chr7:146645600-146647200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
34	chr7:146645800-146646400	Enhancers	Primary neutrophils fromperipheralblood	blood
35	chr7:146645800-146646400	Enhancers	Fetal Heart	heart
36	chr7:146645800-146646400	Enhancers	Monocytes-CD14+_RO01746	blood
37	chr7:146645800-146647000	Enhancers	Primary monocytes fromperipheralblood	blood
38	chr7:146646000-146646600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
39	chr7:146646000-146647000	Enhancers	Primary hematopoietic stem cells	blood
40	chr7:146646600-146647600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chr7:146649400-146650000	Enhancers	Primary hematopoietic stem cells short term culture	blood
42	chr7:146653000-146654600	Enhancers	Fetal Lung	lung
43	chr7:146653200-146654000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
44	chr7:146653400-146653800	Enhancers	Ovary	ovary
45	chr7:146653400-146654000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
46	chr7:146653400-146654000	Enhancers	Fetal Brain Female	brain
47	chr7:146653400-146654400	Enhancers	Fetal Heart	heart
48	chr7:146653800-146654600	Enhancers	Brain Germinal Matrix	brain
49	chr7:146654000-146658600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
50	chr7:146654400-146657800	Weak transcription	Fetal Heart	heart

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links