Variant report

Variant	esv1794696
Chromosome Location	chr7:151023630-151049503
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1431)
CpG islands
(count:1038)
Chromatin interactive
region (count:36)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1431 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:151036647-151037100	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:151046914-151047414	HepG2	liver:	n/a	n/a
3	ARID3A	chr7:151046922-151047613	K562	blood:	n/a	n/a
4	ATF1	chr7:151024899-151024933	K562	blood:	n/a	n/a
5	ATF1	chr7:151046909-151047641	K562	blood:	n/a	n/a
6	ATF2	chr7:151046622-151047634	GM12878	blood:	n/a	n/a
7	ATF2	chr7:151033255-151033770	GM12878	blood:	n/a	n/a
8	ATF2	chr7:151049079-151049660	GM12878	blood:	n/a	n/a
9	ATF2	chr7:151045987-151046453	GM12878	blood:	n/a	n/a
10	ATF2	chr7:151048943-151049614	GM12878	blood:	n/a	n/a
11	ATF2	chr7:151036720-151037481	GM12878	blood:	n/a	n/a
12	ATF2	chr7:151039179-151039938	GM12878	blood:	n/a	n/a
13	ATF2	chr7:151039150-151039918	GM12878	blood:	n/a	n/a
14	ATF2	chr7:151046704-151047650	GM12878	blood:	n/a	n/a
15	ATF3	chr7:151046891-151047689	K562	blood:	n/a	n/a
16	ATF3	chr7:151038735-151039028	K562	blood:	n/a	n/a
17	BACH1	chr7:151039218-151039399	K562	blood:	n/a	n/a
18	BACH1	chr7:151038746-151039086	H1-hESC	embryonic stem cell:	n/a	n/a
19	BATF	chr7:151039233-151039758	GM12878	blood:	n/a	chr7:151039653-151039661
20	BATF	chr7:151043405-151043835	GM12878	blood:	n/a	n/a
21	BATF	chr7:151046937-151047391	GM12878	blood:	n/a	n/a
22	BATF	chr7:151036970-151037448	GM12878	blood:	n/a	n/a
23	BATF	chr7:151039351-151039725	GM12878	blood:	n/a	chr7:151039653-151039661
24	BATF	chr7:151037054-151037441	GM12878	blood:	n/a	n/a
25	BATF	chr7:151033450-151033712	GM12878	blood:	n/a	chr7:151033579-151033590
26	BATF	chr7:151046862-151047668	GM12878	blood:	n/a	n/a
27	BCL11A	chr7:151047181-151047566	GM12878	blood:	n/a	n/a
28	BCL11A	chr7:151039463-151039724	GM12878	blood:	n/a	chr7:151039570-151039579 chr7:151039662-151039671 chr7:151039538-151039547
29	BCL11A	chr7:151046940-151047657	GM12878	blood:	n/a	n/a
30	BCL11A	chr7:151039353-151039712	GM12878	blood:	n/a	chr7:151039417-151039426 chr7:151039570-151039579 chr7:151039662-151039671 chr7:151039538-151039547
31	BCL3	chr7:151042734-151042992	GM12878	blood:	n/a	n/a
32	BCLAF1	chr7:151036945-151037505	GM12878	blood:	n/a	n/a
33	BCLAF1	chr7:151039260-151039817	GM12878	blood:	n/a	chr7:151039417-151039426 chr7:151039570-151039579 chr7:151039662-151039671 chr7:151039538-151039547
34	BCLAF1	chr7:151048959-151049507	GM12878	blood:	n/a	chr7:151049151-151049160
35	BCLAF1	chr7:151046875-151047629	GM12878	blood:	n/a	n/a
36	BCLAF1	chr7:151046929-151047662	GM12878	blood:	n/a	n/a
37	BHLHE40	chr7:151046561-151047715	GM12878	blood:	n/a	n/a
38	BHLHE40	chr7:151036498-151037454	GM12878	blood:	n/a	n/a
39	BHLHE40	chr7:151046517-151047694	K562	blood:	n/a	n/a
40	BHLHE40	chr7:151039265-151040101	GM12878	blood:	n/a	n/a
41	BHLHE40	chr7:151048218-151048374	GM12878	blood:	n/a	n/a
42	BHLHE40	chr7:151038880-151039009	GM12878	blood:	n/a	n/a
43	BHLHE40	chr7:151038527-151039070	K562	blood:	n/a	chr7:151039036-151039052
44	BRCA1	chr7:151046625-151046920	GM12878	blood:	n/a	n/a
45	CBX3	chr7:151038402-151039055	K562	blood:	n/a	n/a
46	CBX3	chr7:151046769-151047777	K562	blood:	n/a	n/a
47	CCNT2	chr7:151046672-151047136	K562	blood:	n/a	n/a
48	CCNT2	chr7:151038560-151039172	K562	blood:	n/a	n/a
49	CEBPB	chr7:151043028-151043531	Hela-S3	cervix:	n/a	n/a
50	CEBPB	chr7:151047127-151047292	HepG2	liver:	n/a	n/a

(count:1038 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:151047520-151047570	NHBE	bronchial:	n/a
2	chr7:151047520-151047570	NHBE	bronchial:	n/a
3	chr7:151038719-151038769	BJ	skin:	n/a
4	chr7:151038942-151038992	Hepatocyte	liver:	n/a
5	chr7:151037549-151037599	ECC-1	luminal epithelium:	n/a
6	chr7:151038742-151038792	NHDF-neo	bronchial:	n/a
7	chr7:151038703-151038753	AG09319	gingival:	n/a
8	chr7:151038594-151038644	GM06990	blood:	n/a
9	chr7:151042396-151042446	BE2_C	brain:	n/a
10	chr7:151036715-151036765	NT2-D1	testis:	n/a
11	chr7:151036715-151036765	BJ	skin:	n/a
12	chr7:151047520-151047570	SAEC	small airway:	n/a
13	chr7:151039078-151039128	ProgFib	skin:	n/a
14	chr7:151039078-151039128	A549	lung:	n/a
15	chr7:151038698-151038748	A549	lung:	n/a
16	chr7:151042396-151042446	NB4	blood:	n/a
17	chr7:151036715-151036765	AG04449	skin:	fetal
18	chr7:151038942-151038992	ProgFib	skin:	n/a
19	chr7:151038594-151038644	ECC-1	luminal epithelium:	n/a
20	chr7:151038698-151038748	ECC-1	luminal epithelium:	n/a
21	chr7:151038594-151038644	GM12892	blood:	n/a
22	chr7:151026011-151026061	HL-60	blood:	n/a
23	chr7:151037527-151037577	GM12892	blood:	n/a
24	chr7:151042396-151042446	BJ	skin:	n/a
25	chr7:151038742-151038792	HIPEpiC	eye:	n/a
26	chr7:151038742-151038792	NB4	blood:	n/a
27	chr7:151038660-151038710	Hela-S3	cervix:	n/a
28	chr7:151037549-151037599	SKMC	muscle:	n/a
29	chr7:151038594-151038644	SKMC	muscle:	n/a
30	chr7:151037527-151037577	PrEC	prostate:	n/a
31	chr7:151038949-151038999	HRE	kidney:	n/a
32	chr7:151038698-151038748	HEK293	kidney:	embryo
33	chr7:151038742-151038792	HCT-116	colon:	n/a
34	chr7:151037549-151037599	LNCaP	prostate:	n/a
35	chr7:151042396-151042446	SK-N-SH	brain:	n/a
36	chr7:151042396-151042446	AG04450	lung:	fetal
37	chr7:151047520-151047570	MCF10A-Er-Src	breast:	n/a
38	chr7:151038942-151038992	HIPEpiC	eye:	n/a
39	chr7:151038949-151038999	AoSMC	blood vessel:	n/a
40	chr7:151038660-151038710	HCPEpiC	choroid plexus:	n/a
41	chr7:151026011-151026061	MCF10A-Er-Src	breast:	n/a
42	chr7:151026011-151026061	IMR90	lung:	fetal
43	chr7:151038742-151038792	HRE	kidney:	n/a
44	chr7:151038719-151038769	Caco-2	colon:	n/a
45	chr7:151036715-151036765	ovcar-3	ovarian:	n/a
46	chr7:151038698-151038748	IMR90	lung:	fetal
47	chr7:151038703-151038753	PFSK-1	brain:	n/a
48	chr7:151038949-151038999	H1-hESC	embryonic stem cell:	embryo
49	chr7:151038942-151038992	HPAEpiC	pulmonary alveolar:	n/a
50	chr7:151038446-151038496	HL-60	blood:	n/a

(count:36 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:151015827..151017496-chr7:151044887..151046581,2	K562	blood:
2	chr7:151037686..151040795-chr7:151041749..151046286,7	MCF-7	breast:
3	chr7:150899283..150901637-chr7:151035774..151038762,2	K562	blood:
4	chr7:150825310..150827714-chr7:151037547..151039688,2	K562	blood:
5	chr7:151033837..151035458-chr7:151037239..151039388,2	MCF-7	breast:
6	chr7:151039491..151042064-chr7:151177845..151180645,2	K562	blood:
7	chr7:151011871..151012769-chr7:151039640..151040156,2	MCF-7	breast:
8	chr22:41842765..41843346-chr7:151038918..151039863,2	Hela-S3	cervix:
9	chr7:151043610..151045202-chr7:151090101..151092800,2	K562	blood:
10	chr7:151039898..151044376-chr7:151046484..151049305,5	MCF-7	breast:
11	chr7:151015904..151017496-chr7:151044887..151047703,2	K562	blood:
12	chr7:151027979..151030667-chr7:151041372..151043584,2	K562	blood:
13	chr7:150971574..150974411-chr7:151038667..151040359,3	K562	blood:
14	chr7:151039898..151044376-chr7:151046484..151049305,5	MCF-7	breast:
15	chr7:151036395..151039308-chr7:151063026..151066018,3	K562	blood:
16	chr7:150971574..150973333-chr7:151038730..151040359,2	K562	blood:
17	chr7:150930547..150933438-chr7:151037429..151040414,2	MCF-7	breast:
18	chr7:151027136..151029304-chr7:151034549..151036958,2	K562	blood:
19	chr7:150932407..150934552-chr7:151037359..151040324,2	K562	blood:
20	chr7:151047952..151050836-chr7:151057197..151059669,2	K562	blood:
21	chr7:151029706..151031731-chr7:151033445..151035496,2	MCF-7	breast:
22	chr7:151038659..151040340-chr7:151041738..151045830,5	MCF-7	breast:
23	chr7:151011867..151012792-chr7:151046918..151048035,4	K562	blood:
24	chr7:151027136..151029304-chr7:151034549..151036958,2	K562	blood:
25	chr7:151038659..151040340-chr7:151041738..151045830,5	MCF-7	breast:
26	chr7:151037686..151040795-chr7:151041749..151046286,7	MCF-7	breast:
27	chr7:150929647..150931224-chr7:151029766..151031795,2	MCF-7	breast:
28	chr7:151031921..151034543-chr7:151036343..151038767,2	K562	blood:
29	chr7:151020134..151022018-chr7:151036761..151038559,2	MCF-7	breast:
30	chr7:151006336..151009328-chr7:151045364..151047522,2	K562	blood:
31	chr7:151007318..151008221-chr7:151047017..151047762,2	MCF-7	breast:
32	chr7:151016234..151019042-chr7:151024588..151026100,2	K562	blood:
33	chr7:151029706..151031731-chr7:151033445..151035496,2	MCF-7	breast:
34	chr7:150972599..150974856-chr7:151038814..151040776,2	MCF-7	breast:
35	chr7:151031921..151034543-chr7:151036343..151038767,2	K562	blood:
36	chr7:151019060..151021479-chr7:151026511..151028085,2	K562	blood:

No data

Variant related genes	Relation type
NUB1	TF binding region
NUB1	CpG island
ENSG00000082014	chromatin interactions
ENSG00000033100	chromatin interactions
ENSG00000013374	chromatin interactions
ENSG00000133612	chromatin interactions
ENSG00000183864	chromatin interactions

Extended variants
information (count: 998 )
Associated
traits (count: 94 )

Variant overlapped rSNPs/rCNVs (count:998 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs79699534	chr7:151023630-151023631	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
2	rs537723572	chr7:151023657-151023658	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs564516983	chr7:151023680-151023681	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs576006270	chr7:151023683-151023684	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs79404961	chr7:151023703-151023704	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs191170787	chr7:151023795-151023796	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs558745905	chr7:151023855-151023856	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs182256965	chr7:151023895-151023896	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs146625382	chr7:151023904-151023905	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs577272478	chr7:151023905-151023906	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs6961795	chr7:151023921-151023922	Weak transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs566917911	chr7:151023937-151023938	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs545121988	chr7:151023943-151023944	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs541214365	chr7:151023950-151023951	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs186922660	chr7:151023951-151023952	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs374362815	chr7:151023966-151023967	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs191869599	chr7:151024042-151024043	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs553531455	chr7:151024061-151024062	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs34109110	chr7:151024165-151024166	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs34280049	chr7:151024184-151024185	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs530264859	chr7:151024190-151024191	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
22	rs542522064	chr7:151024207-151024208	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs185241198	chr7:151024220-151024221	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs530005069	chr7:151024223-151024224	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs189825036	chr7:151024232-151024233	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs560211832	chr7:151024306-151024307	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs10224549	chr7:151024319-151024320	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs552333872	chr7:151024393-151024394	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs75224044	chr7:151024430-151024431	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs537291771	chr7:151024438-151024439	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs35830297	chr7:151024477-151024478	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs76950564	chr7:151024515-151024516	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs569543784	chr7:151024541-151024542	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs116447188	chr7:151024572-151024573	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs536970681	chr7:151024589-151024590	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs553066622	chr7:151024603-151024604	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs376625681	chr7:151024630-151024631	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs538733434	chr7:151024660-151024661	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs552213527	chr7:151024691-151024692	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs575094223	chr7:151024743-151024744	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs200644855	chr7:151024762-151024763	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs10270263	chr7:151024795-151024796	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs554758944	chr7:151024809-151024810	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs574616783	chr7:151024887-151024888	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs193155664	chr7:151024950-151024951	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs144939529	chr7:151024957-151024958	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs17705456	chr7:151024986-151024987	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
48	rs185437991	chr7:151024987-151024988	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs115839482	chr7:151025092-151025093	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs572904519	chr7:151025124-151025125	Enhancers Weak transcription	n/a	n/a	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
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
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1366 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:151017200-151025400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr7:151019800-151029800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr7:151023600-151024200	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr7:151024200-151024600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
5	chr7:151024400-151025200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr7:151024600-151025000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
7	chr7:151024800-151025600	Enhancers	NHLF	lung
8	chr7:151025000-151025600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr7:151025000-151025600	Enhancers	HUES48 Cell Line	embryonic stem cell
10	chr7:151025000-151025600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
11	chr7:151025000-151026200	Enhancers	Small Intestine	intestine
12	chr7:151025000-151029600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
13	chr7:151025200-151026400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
14	chr7:151025400-151025600	Enhancers	iPS-20b Cell Line	embryonic stem cell
15	chr7:151025400-151026200	Enhancers	H9 Cell Line	embryonic stem cell
16	chr7:151025400-151026200	Enhancers	HUES6 Cell Line	embryonic stem cell
17	chr7:151025400-151026200	Enhancers	iPS-15b Cell Line	embryonic stem cell
18	chr7:151025400-151026200	Enhancers	iPS-18 Cell Line	embryonic stem cell
19	chr7:151025400-151026200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
20	chr7:151025600-151025800	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
21	chr7:151025600-151026200	Enhancers	H1 Cell Line	embryonic stem cell
22	chr7:151025600-151026200	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
23	chr7:151025600-151026200	Enhancers	HUES64 Cell Line	embryonic stem cell
24	chr7:151025800-151026000	Enhancers	iPS-20b Cell Line	embryonic stem cell
25	chr7:151026000-151026200	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
26	chr7:151026200-151029600	Weak transcription	HUES48 Cell Line	embryonic stem cell
27	chr7:151026200-151029600	Weak transcription	HUES6 Cell Line	embryonic stem cell
28	chr7:151029600-151029800	Enhancers	iPS-18 Cell Line	embryonic stem cell
29	chr7:151029600-151030000	Enhancers	HUES48 Cell Line	embryonic stem cell
30	chr7:151029600-151030000	Enhancers	HUES6 Cell Line	embryonic stem cell
31	chr7:151029600-151030000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr7:151029600-151030000	Enhancers	Adipose Nuclei	Adipose
33	chr7:151029800-151030000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
34	chr7:151029800-151030600	Bivalent Enhancer	HepG2	liver
35	chr7:151031200-151032800	Enhancers	GM12878-XiMat	blood
36	chr7:151032800-151033400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
37	chr7:151032800-151036800	ZNF genes & repeats	GM12878-XiMat	blood
38	chr7:151033200-151033600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
39	chr7:151033400-151034000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
40	chr7:151033600-151033800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
41	chr7:151033800-151034600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
42	chr7:151034000-151037400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
43	chr7:151034600-151034800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
44	chr7:151034800-151038200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
45	chr7:151035800-151038400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
46	chr7:151035800-151038800	Enhancers	Primary monocytes fromperipheralblood	blood
47	chr7:151036000-151036600	Enhancers	HepG2	liver
48	chr7:151036000-151038200	Weak transcription	Right Atrium	heart
49	chr7:151036200-151036400	Enhancers	Monocytes-CD14+_RO01746	blood
50	chr7:151036200-151036600	Enhancers	Primary neutrophils fromperipheralblood	blood

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