Variant report

Variant	nsv971515
Chromosome Location	chr7:150905324-150908880
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	BACH1	chr7:150907706-150907770	H1-hESC	embryonic stem cell:	n/a	n/a
2	CTCF	chr7:150908320-150908470	WERI-Rb-1	eye:	n/a	chr7:150908426-150908444 chr7:150908421-150908442 chr7:150908433-150908441
3	CTCF	chr7:150908240-150908390	GM06990	blood:	n/a	n/a
4	CTCF	chr7:150908380-150908530	A549	lung:	n/a	chr7:150908426-150908444 chr7:150908421-150908442 chr7:150908433-150908441
5	CTCF	chr7:150908420-150908570	SK-N-SH_RA	brain:	n/a	chr7:150908426-150908444 chr7:150908421-150908442 chr7:150908433-150908441
6	CTCF	chr7:150908411-150908465	K562	blood:	n/a	chr7:150908426-150908444 chr7:150908421-150908442 chr7:150908433-150908441
7	CTCF	chr7:150908326-150908527	H1-hESC	embryonic stem cell:	n/a	chr7:150908426-150908444 chr7:150908421-150908442 chr7:150908433-150908441
8	CTCF	chr7:150908419-150908506	H1-hESC	embryonic stem cell:	n/a	chr7:150908426-150908444 chr7:150908421-150908442 chr7:150908433-150908441
9	CTCF	chr7:150908420-150908461	K562	blood:	n/a	chr7:150908426-150908444 chr7:150908421-150908442 chr7:150908433-150908441
10	CTCF	chr7:150908360-150908510	HBMEC	blood vessel:	n/a	chr7:150908426-150908444 chr7:150908421-150908442 chr7:150908433-150908441
11	CTCF	chr7:150908340-150908490	SK-N-SH_RA	brain:	n/a	chr7:150908426-150908444 chr7:150908421-150908442 chr7:150908433-150908441
12	CTCF	chr7:150908300-150908450	HEK293	kidney:	n/a	chr7:150908426-150908444 chr7:150908421-150908442 chr7:150908433-150908441
13	CTCF	chr7:150908418-150908439	Hela-S3	cervix:	n/a	n/a
14	CTCF	chr7:150908420-150908570	BE2_C	brain:	n/a	chr7:150908426-150908444 chr7:150908421-150908442 chr7:150908433-150908441
15	CTCF	chr7:150906440-150906590	WERI-Rb-1	eye:	n/a	chr7:150906551-150906569 chr7:150906553-150906566
16	JUND	chr7:150907728-150907736	H1-hESC	embryonic stem cell:	n/a	n/a
17	MAFF	chr7:150908296-150908842	K562	blood:	n/a	chr7:150908641-150908659
18	MAFF	chr7:150908450-150908836	HepG2	liver:	n/a	chr7:150908641-150908659
19	MAFK	chr7:150908416-150908803	H1-hESC	embryonic stem cell:	n/a	chr7:150908643-150908659 chr7:150908642-150908656 chr7:150908644-150908655
20	MAFK	chr7:150908468-150908837	K562	blood:	n/a	chr7:150908643-150908659 chr7:150908642-150908656 chr7:150908644-150908655
21	MAFK	chr7:150908452-150908840	Hela-S3	cervix:	n/a	chr7:150908643-150908659 chr7:150908642-150908656 chr7:150908644-150908655
22	MAFK	chr7:150908482-150908840	HepG2	liver:	n/a	chr7:150908643-150908659 chr7:150908642-150908656 chr7:150908644-150908655
23	MAFK	chr7:150908464-150908844	HepG2	liver:	n/a	chr7:150908643-150908659 chr7:150908642-150908656 chr7:150908644-150908655
24	MAFK	chr7:150908240-150908839	IMR90	lung:	n/a	chr7:150908643-150908659 chr7:150908642-150908656 chr7:150908644-150908655
25	PML	chr7:150906503-150907137	K562	blood:	n/a	n/a
26	POLR2A	chr7:150908230-150909218	PANC-1	pancreas:	n/a	n/a
27	POLR2A	chr7:150906647-150906668	IMR90	lung:	n/a	n/a
28	POLR2A	chr7:150906969-150907472	GM12891	blood:	n/a	n/a
29	POLR2A	chr7:150905328-150905960	GM12891	blood:	n/a	n/a
30	POLR2A	chr7:150906075-150906210	Hela-S3	cervix:	n/a	n/a
31	POLR2A	chr7:150907088-150907313	HCT-116	colon:	n/a	n/a
32	POLR2A	chr7:150908869-150909134	SK-N-SH	brain:	n/a	n/a
33	POLR2A	chr7:150906391-150910223	SK-N-MC	brain:	n/a	n/a
34	POLR2A	chr7:150907970-150908818	HepG2	liver:	n/a	n/a
35	POLR2A	chr7:150906323-150907343	H1-hESC	embryonic stem cell:	n/a	n/a
36	POLR2A	chr7:150908663-150909116	GM12891	blood:	n/a	n/a
37	POLR2A	chr7:150906044-150906284	GM12878	blood:	n/a	n/a
38	POLR2A	chr7:150908275-150908537	GM12878	blood:	n/a	n/a
39	POLR2A	chr7:150903836-150905879	MCF10A-Er-Src	breast:	n/a	n/a
40	POLR2A	chr7:150907518-150908587	PANC-1	pancreas:	n/a	n/a
41	POLR2A	chr7:150903888-150910558	K562	blood:	n/a	n/a
42	POLR2A	chr7:150908328-150908598	GM12892	blood:	n/a	n/a
43	POLR2A	chr7:150906044-150906891	GM12892	blood:	n/a	n/a
44	POLR2A	chr7:150908275-150909676	A549	lung:	n/a	n/a
45	POLR2A	chr7:150906064-150906306	H1-hESC	embryonic stem cell:	n/a	n/a
46	POLR2A	chr7:150908598-150908971	HL-60	blood:	n/a	n/a
47	POLR2A	chr7:150908679-150909022	GM12878	blood:	n/a	n/a
48	POLR2A	chr7:150908062-150909373	K562	blood:	n/a	n/a
49	POLR2A	chr7:150906969-150906995	HepG2	liver:	n/a	n/a
50	POLR2A	chr7:150906035-150907560	K562	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:150907018-150907068	SK-N-SH_RA	brain:	n/a
2	chr7:150907018-150907068	GM12891	blood:	n/a
3	chr7:150907018-150907068	SK-N-SH	brain:	n/a
4	chr7:150907018-150907068	HMEC	breast:	n/a
5	chr7:150907018-150907068	AG09319	gingival:	n/a
6	chr7:150907018-150907068	HUVEC	blood vessel:	n/a
7	chr7:150907018-150907068	MCF-7	breast:	n/a
8	chr7:150907018-150907068	ProgFib	skin:	n/a
9	chr7:150907018-150907068	HCF	heart:	n/a
10	chr7:150907018-150907068	HRCEpiC	kidney:	n/a
11	chr7:150907018-150907068	AoSMC	blood vessel:	n/a
12	chr7:150907018-150907068	SK-N-MC	brain:	n/a
13	chr7:150907018-150907068	BJ	skin:	n/a
14	chr7:150907018-150907068	HRE	kidney:	n/a
15	chr7:150907018-150907068	HEK293	kidney:	embryo
16	chr7:150907018-150907068	GM19239	blood:	n/a
17	chr7:150907018-150907068	NT2-D1	testis:	n/a
18	chr7:150907018-150907068	PANC-1	pancreas:	n/a
19	chr7:150907018-150907068	LNCaP	prostate:	n/a
20	chr7:150907018-150907068	NHDF-neo	bronchial:	n/a
21	chr7:150907018-150907068	U87	brain:	n/a
22	chr7:150907018-150907068	CMK	blood:	n/a
23	chr7:150907018-150907068	HCT-116	colon:	n/a
24	chr7:150907018-150907068	HL-60	blood:	n/a
25	chr7:150907018-150907068	Hepatocyte	liver:	n/a
26	chr7:150907018-150907068	GM06990	blood:	n/a
27	chr7:150907018-150907068	HPAEpiC	pulmonary alveolar:	n/a
28	chr7:150907018-150907068	RPTEC	kidney:	n/a
29	chr7:150907018-150907068	HEEpiC	esophagus:	n/a
30	chr7:150907018-150907068	NHBE	bronchial:	n/a
31	chr7:150907018-150907068	K562	blood:	n/a
32	chr7:150907018-150907068	Jurkat	blood:	n/a
33	chr7:150907018-150907068	BE2_C	brain:	n/a
34	chr7:150907018-150907068	HRPEpiC	eye:	n/a
35	chr7:150907018-150907068	IMR90	lung:	fetal
36	chr7:150907018-150907068	PFSK-1	brain:	n/a
37	chr7:150907018-150907068	HNPCEpiC	eye:	n/a
38	chr7:150907018-150907068	SAEC	small airway:	n/a
39	chr7:150907018-150907068	HIPEpiC	eye:	n/a
40	chr7:150907018-150907068	SKMC	muscle:	n/a
41	chr7:150907018-150907068	ECC-1	luminal epithelium:	n/a
42	chr7:150907018-150907068	NH-A	brain:	n/a
43	chr7:150907018-150907068	GM12892	blood:	n/a
44	chr7:150907018-150907068	Hela-S3	cervix:	n/a
45	chr7:150907018-150907068	ovcar-3	ovarian:	n/a
46	chr7:150907018-150907068	HCM	heart:	n/a
47	chr7:150907018-150907068	AG09309	skin:	n/a
48	chr7:150907018-150907068	A549	lung:	n/a
49	chr7:150907018-150907068	H1-hESC	embryonic stem cell:	embryo
50	chr7:150907018-150907068	HepG2	liver:	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:150888866..150891539-chr7:150907679..150909956,2	K562	blood:
2	chr7:150847712..150849868-chr7:150904203..150906196,2	K562	blood:
3	chr6:26199713..26200241-chr7:150905163..150905666,2	NB4	blood:
4	chr7:150905577..150911406-chr7:150912646..150916801,5	MCF-7	breast:
5	chr7:150891021..150894047-chr7:150903190..150905839,3	MCF-7	breast:
6	chr7:150904819..150907851-chr7:150927889..150929495,3	MCF-7	breast:
7	chr7:150869414..150871955-chr7:150904736..150906461,2	K562	blood:
8	chr7:150903033..150905442-chr7:150914497..150916686,3	MCF-7	breast:
9	chr7:150893356..150896342-chr7:150905267..150908010,3	K562	blood:
10	chr7:150908780..150913504-chr7:150916695..150920010,4	MCF-7	breast:
11	chr7:150864964..150867853-chr7:150903647..150905737,2	K562	blood:
12	chr7:150901201..150903051-chr7:150905841..150907689,2	MCF-7	breast:
13	chr7:150900947..150904902-chr7:150906819..150911270,6	MCF-7	breast:
14	chr7:150864964..150867853-chr7:150902641..150905737,3	K562	blood:
15	chr7:150905206..150906764-chr7:150930054..150932100,2	MCF-7	breast:

Variant related genes	Relation type
IQCA1P1	TF binding region
IQCA1P1	CpG island
ENSG00000197846	chromatin interactions
ENSG00000033050	chromatin interactions
ENSG00000183016	chromatin interactions
ENSG00000164900	chromatin interactions

Extended variants
information (count: 158 )
Associated
traits (count: 94 )

Variant overlapped rSNPs/rCNVs (count:158 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs566106308	chr7:150905352-150905353	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
2	rs535244192	chr7:150905418-150905419	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs558446615	chr7:150905423-150905424	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs2608291	chr7:150905444-150905445	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
5	rs537431462	chr7:150905468-150905469	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs191039165	chr7:150905543-150905544	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs114063138	chr7:150905585-150905586	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs182159381	chr7:150905586-150905587	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs147550779	chr7:150905626-150905627	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs553445438	chr7:150905640-150905641	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs185454481	chr7:150905677-150905678	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs11974912	chr7:150905701-150905702	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs564831828	chr7:150905702-150905703	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs77277075	chr7:150905715-150905716	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs371796859	chr7:150905720-150905721	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs142076189	chr7:150905731-150905732	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs543785798	chr7:150905738-150905739	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs190166450	chr7:150905747-150905748	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs529710543	chr7:150905767-150905768	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs368331972	chr7:150905775-150905776	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs546350548	chr7:150905780-150905781	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs566566079	chr7:150905788-150905789	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs534430742	chr7:150905797-150905798	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs183461887	chr7:150905846-150905847	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs552044024	chr7:150905847-150905848	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs571965445	chr7:150905948-150905949	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs188352615	chr7:150905980-150905981	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs35735561	chr7:150906044-150906045	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs530145979	chr7:150906053-150906054	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs537768645	chr7:150906070-150906071	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs550976517	chr7:150906154-150906155	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs567517400	chr7:150906196-150906197	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs574377801	chr7:150906202-150906203	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs200551788	chr7:150906237-150906238	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs553142297	chr7:150906245-150906246	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs573330255	chr7:150906285-150906286	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs538445266	chr7:150906319-150906320	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs75405398	chr7:150906338-150906339	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs193029781	chr7:150906367-150906368	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs576005962	chr7:150906369-150906370	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs371914808	chr7:150906382-150906383	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs116212133	chr7:150906390-150906391	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs149704133	chr7:150906417-150906418	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs73169642	chr7:150906453-150906454	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs183442511	chr7:150906462-150906463	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs564684860	chr7:150906500-150906501	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs540232121	chr7:150906551-150906552	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs35093688	chr7:150906554-150906555	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs77379445	chr7:150906613-150906614	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs551980816	chr7:150906626-150906627	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:94)

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
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	17603634	CNVD
Urothelial carcinoma	18382360	CNVD
Myelodysplastic syndrome	17634407	CNVD
Multiple myeloma	16461302	CNVD
Neuroblastoma	18923191	CNVD
Schizophrenia	17646849	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Acute myeloid leukemia	16864856	CNVD
Autism	20808228	CNVD
Breast cancer	21509527	CNVD
Ovarian cancer	21720365	CNVD
Heart disease	21282601	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21045282	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Glioblastoma multiforme	17002787	CNVD
Lobular carcinoma	20920651	CNVD
Long-qt syndrome	20920651	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Liver carcinoma	19366792	CNVD
Long-qt syndrome	17576883	CNVD
Bradycardia syndrome	17576883	CNVD
Sudden cardiac death	19188705	CNVD
renal disease	17924346	CNVD
Ovarian cancer	21781307	CNVD
Adrenocortical carcinoma	18281524	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Pancreatic cancer	17952125	CNVD
Schizophrenia	20838587	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:191 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:150885000-150910000	Weak transcription	Right Atrium	heart
2	chr7:150899000-150909600	Weak transcription	Aorta	Aorta
3	chr7:150901800-150910000	Weak transcription	Ovary	ovary
4	chr7:150902000-150906000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
5	chr7:150902000-150910200	Weak transcription	Right Ventricle	heart
6	chr7:150902000-150910400	Weak transcription	Pancreas	Pancrea
7	chr7:150902400-150907000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr7:150902600-150905800	Enhancers	Primary T helper cells fromperipheralblood	blood
9	chr7:150902800-150905600	Enhancers	Primary T killer memory cells from peripheral blood	blood
10	chr7:150903000-150905400	Enhancers	Primary T helper cells PMA-I stimulated	--
11	chr7:150903000-150905800	Enhancers	Primary hematopoietic stem cells short term culture	blood
12	chr7:150903000-150905800	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
13	chr7:150903000-150905800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
14	chr7:150903000-150908800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
15	chr7:150903200-150905400	Enhancers	Primary T helper naive cells from peripheral blood	blood
16	chr7:150903200-150906600	Enhancers	Primary hematopoietic stem cells	blood
17	chr7:150903200-150909600	Weak transcription	Spleen	Spleen
18	chr7:150903600-150905400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
19	chr7:150903800-150905400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
20	chr7:150903800-150905400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr7:150904000-150906800	Enhancers	Primary T cells fromperipheralblood	blood
22	chr7:150904000-150909000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
23	chr7:150904200-150908000	Weak transcription	Brain Cingulate Gyrus	brain
24	chr7:150904400-150905800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
25	chr7:150904400-150909600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
26	chr7:150904600-150906000	Enhancers	Fetal Lung	lung
27	chr7:150904600-150909600	Weak transcription	Psoas Muscle	Psoas
28	chr7:150904600-150909600	Weak transcription	Rectal Mucosa Donor 29	rectum
29	chr7:150904800-150905600	Enhancers	Duodenum Mucosa	Duodenum
30	chr7:150904800-150907600	Weak transcription	Skeletal Muscle Male	skeletal muscle
31	chr7:150904800-150908600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
32	chr7:150904800-150908800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr7:150904800-150909200	Weak transcription	GM12878-XiMat	blood
34	chr7:150904800-150909400	Weak transcription	Fetal Thymus	thymus
35	chr7:150905000-150906000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
36	chr7:150905000-150908200	Weak transcription	Primary T cells from cord blood	blood
37	chr7:150905000-150908400	Weak transcription	Brain Inferior Temporal Lobe	brain
38	chr7:150905000-150910000	Weak transcription	Muscle Satellite Cultured Cells	--
39	chr7:150905000-150910000	Weak transcription	Esophagus	oesophagus
40	chr7:150905000-150910800	Weak transcription	Colonic Mucosa	Colon
41	chr7:150905200-150908000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
42	chr7:150905200-150908600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
43	chr7:150905200-150909200	Weak transcription	K562	blood
44	chr7:150905200-150909600	Weak transcription	Gastric	stomach
45	chr7:150905200-150910000	Weak transcription	Primary B cells from peripheral blood	blood
46	chr7:150905200-150910200	Weak transcription	A549	lung
47	chr7:150905400-150906400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
48	chr7:150905400-150908800	Weak transcription	Fetal Intestine Small	intestine
49	chr7:150905400-150909000	Weak transcription	Fetal Muscle Leg	muscle
50	chr7:150905400-150909400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood

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