Variant report

Variant	nsv981608
Chromosome Location	chr7:150002640-150009746
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:109)
CpG islands
(count:61)
Chromatin interactive
region (count:14)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:109 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:150004069-150004434	K562	blood:	n/a	n/a
2	ARID3A	chr7:150003045-150003176	K562	blood:	n/a	n/a
3	ATF1	chr7:150004234-150004547	K562	blood:	n/a	n/a
4	ATF1	chr7:150002546-150002653	K562	blood:	n/a	n/a
5	ATF1	chr7:150008934-150009120	K562	blood:	n/a	n/a
6	BACH1	chr7:150004249-150004357	K562	blood:	n/a	n/a
7	BHLHE40	chr7:150002428-150002740	K562	blood:	n/a	n/a
8	BHLHE40	chr7:150004337-150004505	K562	blood:	n/a	n/a
9	BRCA1	chr7:150004406-150004492	Hela-S3	cervix:	n/a	n/a
10	CBX3	chr7:150002345-150002822	K562	blood:	n/a	n/a
11	CBX3	chr7:150004208-150004572	HCT-116	colon:	n/a	n/a
12	CBX3	chr7:150004138-150004672	K562	blood:	n/a	n/a
13	CBX3	chr7:150004239-150004629	K562	blood:	n/a	n/a
14	CEBPB	chr7:150004309-150004607	Hela-S3	cervix:	n/a	n/a
15	CEBPB	chr7:150003045-150003237	Hela-S3	cervix:	n/a	n/a
16	CUX1	chr7:150009412-150009689	K562	blood:	n/a	n/a
17	E2F6	chr7:150004298-150004463	K562	blood:	n/a	n/a
18	E2F6	chr7:150002410-150002651	K562	blood:	n/a	n/a
19	EGR1	chr7:150002461-150002660	K562	blood:	n/a	n/a
20	EGR1	chr7:150002411-150002668	K562	blood:	n/a	n/a
21	EP300	chr7:150004249-150004549	K562	blood:	n/a	n/a
22	EP300	chr7:150009678-150010250	Hela-S3	cervix:	n/a	n/a
23	EP300	chr7:150002991-150003254	Hela-S3	cervix:	n/a	n/a
24	FOS	chr7:150005136-150005222	MCF10A-Er-Src	breast:	n/a	n/a
25	FOS	chr7:150005139-150005218	MCF10A-Er-Src	breast:	n/a	n/a
26	FOSL1	chr7:150004896-150005385	HCT-116	colon:	n/a	n/a
27	FOSL1	chr7:150004851-150005540	HCT-116	colon:	n/a	n/a
28	FOSL2	chr7:150004377-150004735	HepG2	liver:	n/a	n/a
29	FOXA1	chr7:150004335-150004755	HepG2	liver:	n/a	n/a
30	GATA1	chr7:150008674-150011730	K562	blood:	n/a	n/a
31	GATA2	chr7:150004223-150004652	K562	blood:	n/a	n/a
32	GATA2	chr7:150009740-150010849	K562	blood:	n/a	n/a
33	HEY1	chr7:150002452-150003152	K562	blood:	n/a	n/a
34	HEY1	chr7:150002402-150003025	K562	blood:	n/a	n/a
35	IRF1	chr7:150005346-150005599	K562	blood:	n/a	n/a
36	IRF1	chr7:150005348-150005540	K562	blood:	n/a	n/a
37	IRF1	chr7:150009572-150011606	K562	blood:	n/a	n/a
38	JUN	chr7:150005084-150005284	H1-hESC	embryonic stem cell:	n/a	n/a
39	JUND	chr7:150005076-150005239	H1-hESC	embryonic stem cell:	n/a	n/a
40	JUND	chr7:150002452-150002684	K562	blood:	n/a	n/a
41	JUND	chr7:150004860-150005413	HCT-116	colon:	n/a	n/a
42	JUND	chr7:150004340-150004540	K562	blood:	n/a	n/a
43	JUND	chr7:150005052-150005309	H1-hESC	embryonic stem cell:	n/a	n/a
44	JUND	chr7:150004390-150004577	HepG2	liver:	n/a	n/a
45	KAP1	chr7:150004021-150004810	K562	blood:	n/a	n/a
46	MAFF	chr7:150002977-150003193	K562	blood:	n/a	n/a
47	MAFK	chr7:150003026-150003182	K562	blood:	n/a	n/a
48	MAX	chr7:150002303-150002813	K562	blood:	n/a	chr7:150002525-150002538 chr7:150002527-150002536 chr7:150002526-150002536 chr7:150002522-150002541 chr7:150002526-150002537 chr7:150002526-150002537 chr7:150002526-150002537 chr7:150002525-150002538 chr7:150002527-150002537 chr7:150002526-150002536 chr7:150002527-150002537 chr7:150002525-150002538
49	MAX	chr7:150004267-150004575	K562	blood:	n/a	n/a
50	MAX	chr7:150004363-150004492	K562	blood:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:150004345-150004395	ECC-1	luminal epithelium:	n/a
2	chr7:150004345-150004395	HRPEpiC	eye:	n/a
3	chr7:150004345-150004395	HRE	kidney:	n/a
4	chr7:150004345-150004395	LNCaP	prostate:	n/a
5	chr7:150004345-150004395	NHBE	bronchial:	n/a
6	chr7:150004345-150004395	SAEC	small airway:	n/a
7	chr7:150004345-150004395	SK-N-MC	brain:	n/a
8	chr7:150004345-150004395	Jurkat	blood:	n/a
9	chr7:150004345-150004395	HEK293	kidney:	embryo
10	chr7:150004345-150004395	HCM	heart:	n/a
11	chr7:150004345-150004395	PANC-1	pancreas:	n/a
12	chr7:150004345-150004395	GM12878	blood:	n/a
13	chr7:150004345-150004395	AG09319	gingival:	n/a
14	chr7:150004345-150004395	SK-N-SH	brain:	n/a
15	chr7:150004345-150004395	AG10803	skin:	n/a
16	chr7:150004345-150004395	ovcar-3	ovarian:	n/a
17	chr7:150004345-150004395	IMR90	lung:	fetal
18	chr7:150004345-150004395	AG04449	skin:	fetal
19	chr7:150004345-150004395	SKMC	muscle:	n/a
20	chr7:150004345-150004395	NH-A	brain:	n/a
21	chr7:150004345-150004395	NT2-D1	testis:	n/a
22	chr7:150004345-150004395	NB4	blood:	n/a
23	chr7:150004345-150004395	K562	blood:	n/a
24	chr7:150004345-150004395	MCF10A-Er-Src	breast:	n/a
25	chr7:150004345-150004395	Hela-S3	cervix:	n/a
26	chr7:150004345-150004395	HCPEpiC	choroid plexus:	n/a
27	chr7:150004345-150004395	GM12891	blood:	n/a
28	chr7:150004345-150004395	HRCEpiC	kidney:	n/a
29	chr7:150004345-150004395	HUVEC	blood vessel:	n/a
30	chr7:150004345-150004395	A549	lung:	n/a
31	chr7:150004345-150004395	HMEC	breast:	n/a
32	chr7:150004345-150004395	ProgFib	skin:	n/a
33	chr7:150004345-150004395	HPAEpiC	pulmonary alveolar:	n/a
34	chr7:150004345-150004395	Hepatocyte	liver:	n/a
35	chr7:150004345-150004395	SK-N-SH_RA	brain:	n/a
36	chr7:150004345-150004395	U87	brain:	n/a
37	chr7:150004345-150004395	GM19239	blood:	n/a
38	chr7:150004345-150004395	PFSK-1	brain:	n/a
39	chr7:150004345-150004395	GM12892	blood:	n/a
40	chr7:150004345-150004395	AG09309	skin:	n/a
41	chr7:150004345-150004395	HCT-116	colon:	n/a
42	chr7:150004345-150004395	HepG2	liver:	n/a
43	chr7:150004345-150004395	BJ	skin:	n/a
44	chr7:150004345-150004395	MCF-7	breast:	n/a
45	chr7:150004345-150004395	Caco-2	colon:	n/a
46	chr7:150004345-150004395	GM06990	blood:	n/a
47	chr7:150004345-150004395	HAEpiC	amniotic membrane:	n/a
48	chr7:150004345-150004395	AoSMC	blood vessel:	n/a
49	chr7:150004345-150004395	RPTEC	kidney:	n/a
50	chr7:150004345-150004395	AG04450	lung:	fetal

(count:14 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:150005819..150007873-chr7:150009129..150011102,2	K562	blood:
2	chr7:150009392..150012620-chr7:150013659..150016251,3	MCF-7	breast:
3	chr7:150003788..150006557-chr7:150126189..150128283,2	K562	blood:
4	chr7:150008263..150011121-chr7:150102492..150104771,2	K562	blood:
5	chr7:150002193..150004738-chr7:150017976..150020637,3	K562	blood:
6	chr7:150004469..150007293-chr7:150009416..150012608,5	K562	blood:
7	chr7:150005819..150007873-chr7:150009129..150011102,2	K562	blood:
8	chr7:150007648..150010098-chr7:150018612..150020930,2	MCF-7	breast:
9	chr7:150006854..150009038-chr7:150044766..150046697,2	MCF-7	breast:
10	chr7:150009132..150011651-chr7:150053831..150057388,3	K562	blood:
11	chr7:150004469..150007293-chr7:150009416..150012608,5	K562	blood:
12	chr7:150002516..150004738-chr7:150017976..150020518,2	K562	blood:
13	chr7:150005371..150007038-chr7:150019861..150021665,2	K562	blood:
14	chr7:150004511..150006297-chr7:150063886..150065749,2	K562	blood:

No data

Variant related genes	Relation type
ACTR3C	TF binding region
ACTR3C	CpG island
ENSG00000196456	chromatin interactions
ENSG00000214022	chromatin interactions
ENSG00000127399	chromatin interactions
ENSG00000106526	chromatin interactions

Extended variants
information (count: 303 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:303 , 50 per page) page: 1 2 3 4 5 6 7

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs553507104	chr7:150002652-150002653	Weak transcription Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs3854303	chr7:150002715-150002716	Weak transcription Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs151174037	chr7:150002716-150002717	Weak transcription Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs564221212	chr7:150002728-150002729	Weak transcription Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs367713030	chr7:150002737-150002738	Weak transcription Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs544694355	chr7:150002762-150002763	Weak transcription Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs2531009	chr7:150002773-150002774	Weak transcription Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs2531008	chr7:150002789-150002790	Weak transcription Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs564647717	chr7:150002807-150002808	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs11766288	chr7:150002815-150002816	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
11	rs2531007	chr7:150002841-150002842	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs185996549	chr7:150002845-150002846	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs10952249	chr7:150002859-150002860	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
14	rs529980589	chr7:150002898-150002899	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs191290665	chr7:150002924-150002925	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs566664802	chr7:150002945-150002946	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs2689438	chr7:150002993-150002994	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs114205512	chr7:150002995-150002996	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs551853637	chr7:150003023-150003024	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs181358534	chr7:150003066-150003067	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs537015261	chr7:150003073-150003074	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs557306547	chr7:150003119-150003120	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs567579721	chr7:150003140-150003141	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs375727181	chr7:150003166-150003167	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs528919917	chr7:150003173-150003174	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs141972593	chr7:150003203-150003204	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs55869606	chr7:150003208-150003209	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs573060290	chr7:150003230-150003231	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs538848683	chr7:150003237-150003238	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs558201394	chr7:150003249-150003250	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs550243913	chr7:150003265-150003266	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs185590390	chr7:150003273-150003274	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs190449212	chr7:150003370-150003371	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs56649777	chr7:150003446-150003447	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs141257484	chr7:150003453-150003454	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs540483549	chr7:150003469-150003470	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs560467067	chr7:150003560-150003561	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs532319617	chr7:150003589-150003590	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs552418243	chr7:150003593-150003594	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs2907033	chr7:150003614-150003615	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs183036728	chr7:150003623-150003624	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs2907032	chr7:150003627-150003628	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs568862999	chr7:150003634-150003635	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs550840376	chr7:150003646-150003647	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs567638765	chr7:150003668-150003669	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs536259768	chr7:150003685-150003686	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs546843356	chr7:150003689-150003690	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs566844283	chr7:150003698-150003699	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs187739657	chr7:150003745-150003746	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs73470356	chr7:150003757-150003758	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	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
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
Congenital long qt syndrome	19214780	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:149984200-150012400	Weak transcription	Liver	Liver
2	chr7:149984200-150019400	Weak transcription	Colonic Mucosa	Colon
3	chr7:149992400-150018000	Weak transcription	Fetal Intestine Small	intestine
4	chr7:150000200-150003200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
5	chr7:150000400-150003200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr7:150000400-150006600	Enhancers	K562	blood
7	chr7:150001200-150003800	Enhancers	Primary neutrophils fromperipheralblood	blood
8	chr7:150001800-150005000	Enhancers	Hela-S3	cervix
9	chr7:150002000-150003000	Enhancers	Fetal Lung	lung
10	chr7:150002200-150002800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr7:150002200-150002800	Enhancers	Brain Anterior Caudate	brain
12	chr7:150002400-150002800	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
13	chr7:150002600-150002800	Enhancers	Primary hematopoietic stem cells	blood
14	chr7:150002600-150003800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
15	chr7:150002600-150004600	Weak transcription	HepG2	liver
16	chr7:150002600-150007200	Weak transcription	Pancreas	Pancrea
17	chr7:150002800-150003600	Weak transcription	Primary hematopoietic stem cells	blood
18	chr7:150003200-150003800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
19	chr7:150003600-150004000	Enhancers	Primary hematopoietic stem cells	blood
20	chr7:150003600-150004400	Enhancers	Fetal Thymus	thymus
21	chr7:150003800-150016000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
22	chr7:150004000-150019000	Weak transcription	Primary hematopoietic stem cells	blood
23	chr7:150004600-150005200	Enhancers	HepG2	liver
24	chr7:150005000-150005200	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
25	chr7:150005000-150005400	Genic enhancers	Hela-S3	cervix
26	chr7:150005200-150010000	Weak transcription	HepG2	liver
27	chr7:150005400-150006600	Enhancers	Hela-S3	cervix
28	chr7:150006600-150007000	Weak transcription	Hela-S3	cervix
29	chr7:150006600-150007000	Weak transcription	K562	blood
30	chr7:150007000-150009200	Enhancers	K562	blood
31	chr7:150007000-150010200	Enhancers	Hela-S3	cervix
32	chr7:150007000-150015000	Weak transcription	Sigmoid Colon	Sigmoid Colon
33	chr7:150007200-150009000	Enhancers	Pancreas	Pancrea
34	chr7:150007600-150007800	Enhancers	HSMM	muscle
35	chr7:150007600-150018000	Weak transcription	Fetal Intestine Large	intestine
36	chr7:150007800-150008800	Weak transcription	HSMM	muscle
37	chr7:150008000-150010400	Enhancers	Fetal Muscle Leg	muscle
38	chr7:150008400-150008600	Enhancers	Gastric	stomach
39	chr7:150008400-150009600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
40	chr7:150008400-150010200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
41	chr7:150008400-150010400	Enhancers	HSMMtube	muscle
42	chr7:150008400-150011200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
43	chr7:150008600-150011000	Weak transcription	Gastric	stomach
44	chr7:150008800-150009000	Bivalent Enhancer	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr7:150008800-150009000	Bivalent Enhancer	H9 Derived Neuron Cultured Cells	ES cell derived
46	chr7:150008800-150009000	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
47	chr7:150008800-150009200	Bivalent Enhancer	H9 Cell Line	embryonic stem cell
48	chr7:150008800-150009200	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
49	chr7:150008800-150009200	Enhancers	Fetal Kidney	kidney
50	chr7:150008800-150009400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived

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