Variant report

Variant	esv1795085
Chromosome Location	chr7:105094664-105116430
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:157)
CpG islands
(count:245)
Chromatin interactive
region (count:20)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:2)

(count:157 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr7:105113653-105113991	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr7:105103081-105103084	K562	blood:	n/a	n/a
3	BACH1	chr7:105113662-105113870	K562	blood:	n/a	n/a
4	CEBPB	chr7:105102081-105102211	HepG2	liver:	n/a	n/a
5	CEBPB	chr7:105094884-105095110	IMR90	lung:	n/a	n/a
6	CEBPB	chr7:105101972-105102318	HepG2	liver:	n/a	n/a
7	CEBPB	chr7:105113607-105113988	IMR90	lung:	n/a	n/a
8	CEBPB	chr7:105104279-105104304	K562	blood:	n/a	chr7:105104289-105104300 chr7:105104289-105104302
9	CEBPB	chr7:105113654-105113964	A549	lung:	n/a	n/a
10	CHD2	chr7:105104575-105104685	K562	blood:	n/a	n/a
11	CTCF	chr7:105113680-105113830	HPAF	blood vessel:	n/a	n/a
12	CTCF	chr7:105113700-105113850	HMEC	breast:	n/a	n/a
13	CTCF	chr7:105113700-105113850	AG04449	skin:	n/a	n/a
14	CTCF	chr7:105113600-105113750	HCM	heart:	n/a	n/a
15	CTCF	chr7:105113640-105113790	HPF	lung:	n/a	n/a
16	CTCF	chr7:105109541-105109612	Kidney_OC	kidney:	n/a	n/a
17	CTCF	chr7:105113600-105113750	AoAF	blood vessel:	n/a	n/a
18	CTCF	chr7:105113700-105113850	HCFaa	heart:	n/a	n/a
19	CTCF	chr7:105113680-105113830	HBMEC	blood vessel:	n/a	n/a
20	CTCF	chr7:105113700-105113850	HMF	breast:	n/a	n/a
21	CTCF	chr7:105113700-105113850	AG09319	gingival:	n/a	n/a
22	CTCF	chr7:105113680-105113830	AG09319	gingival:	n/a	n/a
23	CTCF	chr7:105113720-105113870	HBMEC	blood vessel:	n/a	n/a
24	CTCF	chr7:105113775-105113805	NHEK	skin:	n/a	n/a
25	CTCF	chr7:105113660-105113810	AG10803	skin:	n/a	n/a
26	CTCF	chr7:105113660-105113810	HPAF	blood vessel:	n/a	n/a
27	CTCF	chr7:105113700-105113850	HCPEpiC	choroid plexus:	n/a	n/a
28	CTCF	chr7:105113600-105113750	BJ	skin:	n/a	n/a
29	CTCF	chr7:105113580-105113730	BJ	skin:	n/a	n/a
30	CUX1	chr7:105094699-105094760	K562	blood:	n/a	n/a
31	E2F4	chr7:105106960-105107100	MCF10A-Er-Src	breast:	n/a	n/a
32	EP300	chr7:105094828-105095097	SK-N-SH_RA	brain:	n/a	n/a
33	EP300	chr7:105094800-105095084	SK-N-SH_RA	brain:	n/a	n/a
34	EP300	chr7:105094702-105095253	SK-N-SH	brain:	n/a	chr7:105094793-105094807
35	FAM48A	chr7:105096725-105096890	GM12878	blood:	n/a	n/a
36	FOS	chr7:105101979-105102296	MCF10A-Er-Src	breast:	n/a	n/a
37	FOS	chr7:105114611-105114671	MCF10A-Er-Src	breast:	n/a	n/a
38	FOS	chr7:105113654-105113995	MCF10A-Er-Src	breast:	n/a	n/a
39	FOS	chr7:105095421-105095625	MCF10A-Er-Src	breast:	n/a	chr7:105095476-105095488
40	FOS	chr7:105101993-105102236	MCF10A-Er-Src	breast:	n/a	n/a
41	FOS	chr7:105113642-105114004	MCF10A-Er-Src	breast:	n/a	n/a
42	FOS	chr7:105113636-105114000	MCF10A-Er-Src	breast:	n/a	n/a
43	FOS	chr7:105095425-105095686	MCF10A-Er-Src	breast:	n/a	chr7:105095476-105095488
44	FOS	chr7:105101979-105102235	MCF10A-Er-Src	breast:	n/a	n/a
45	FOS	chr7:105102049-105102249	MCF10A-Er-Src	breast:	n/a	n/a
46	FOS	chr7:105095392-105095618	MCF10A-Er-Src	breast:	n/a	chr7:105095476-105095488
47	FOS	chr7:105113660-105113996	MCF10A-Er-Src	breast:	n/a	n/a
48	FOXA1	chr7:105101919-105102315	HepG2	liver:	n/a	n/a
49	FOXA1	chr7:105101954-105102359	A549	lung:	n/a	n/a
50	FOXA1	chr7:105102024-105102308	A549	lung:	n/a	n/a

(count:245 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:105097168-105097218	AG09319	gingival:	n/a
2	chr7:105097168-105097218	AG09319	gingival:	n/a
3	chr7:105110948-105110998	HL-60	blood:	n/a
4	chr7:105110948-105110998	NT2-D1	testis:	n/a
5	chr7:105094993-105095043	AG04450	lung:	fetal
6	chr7:105112740-105112790	T-47D	breast:	n/a
7	chr7:105112740-105112790	Caco-2	colon:	n/a
8	chr7:105094993-105095043	SK-N-SH_RA	brain:	n/a
9	chr7:105097168-105097218	SK-N-MC	brain:	n/a
10	chr7:105110948-105110998	CMK	blood:	n/a
11	chr7:105110948-105110998	HCF	heart:	n/a
12	chr7:105094993-105095043	AG04449	skin:	fetal
13	chr7:105097168-105097218	HCT-116	colon:	n/a
14	chr7:105112740-105112790	HEK293	kidney:	embryo
15	chr7:105097168-105097218	PFSK-1	brain:	n/a
16	chr7:105097168-105097218	PANC-1	pancreas:	n/a
17	chr7:105112740-105112790	H1-hESC	embryonic stem cell:	embryo
18	chr7:105112740-105112790	CMK	blood:	n/a
19	chr7:105094993-105095043	Hela-S3	cervix:	n/a
20	chr7:105110948-105110998	HIPEpiC	eye:	n/a
21	chr7:105097168-105097218	HEK293	kidney:	embryo
22	chr7:105094993-105095043	NB4	blood:	n/a
23	chr7:105110948-105110998	AG10803	skin:	n/a
24	chr7:105094993-105095043	SAEC	small airway:	n/a
25	chr7:105110948-105110998	HepG2	liver:	n/a
26	chr7:105110948-105110998	LNCaP	prostate:	n/a
27	chr7:105112740-105112790	MCF-7	breast:	n/a
28	chr7:105112740-105112790	SK-N-SH_RA	brain:	n/a
29	chr7:105110948-105110998	MCF-7	breast:	n/a
30	chr7:105097168-105097218	HAEpiC	amniotic membrane:	n/a
31	chr7:105112740-105112790	SAEC	small airway:	n/a
32	chr7:105094993-105095043	SK-N-MC	brain:	n/a
33	chr7:105112740-105112790	GM12891	blood:	n/a
34	chr7:105097168-105097218	Hepatocyte	liver:	n/a
35	chr7:105112740-105112790	ovcar-3	ovarian:	n/a
36	chr7:105094993-105095043	NHDF-neo	bronchial:	n/a
37	chr7:105110948-105110998	AG04450	lung:	fetal
38	chr7:105094993-105095043	HRE	kidney:	n/a
39	chr7:105094993-105095043	ProgFib	skin:	n/a
40	chr7:105097168-105097218	ovcar-3	ovarian:	n/a
41	chr7:105112740-105112790	HEEpiC	esophagus:	n/a
42	chr7:105110948-105110998	NHBE	bronchial:	n/a
43	chr7:105110948-105110998	HRE	kidney:	n/a
44	chr7:105112740-105112790	SK-N-MC	brain:	n/a
45	chr7:105097168-105097218	Caco-2	colon:	n/a
46	chr7:105110948-105110998	T-47D	breast:	n/a
47	chr7:105110948-105110998	ECC-1	luminal epithelium:	n/a
48	chr7:105112740-105112790	BJ	skin:	n/a
49	chr7:105094993-105095043	BJ	skin:	n/a
50	chr7:105094993-105095043	AoSMC	blood vessel:	n/a

(count:20 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:105115487..105117775-chr7:105123011..105125006,2	K562	blood:
2	chr7:105103194..105105383-chr7:105105621..105108054,3	K562	blood:
3	chr7:105095176..105096749-chr7:105098441..105100955,2	MCF-7	breast:
4	chr7:105103194..105105383-chr7:105105621..105108054,3	K562	blood:
5	chr7:105093737..105097449-chr7:105099816..105103606,4	K562	blood:
6	chr7:105069185..105071026-chr7:105110310..105112272,2	MCF-7	breast:
7	chr7:105116272..105117859-chr7:105118414..105120932,2	K562	blood:
8	chr7:105027071..105029412-chr7:105096317..105098709,3	K562	blood:
9	chr7:105027071..105030527-chr7:105095763..105098466,3	K562	blood:
10	chr7:105095176..105096749-chr7:105098441..105100955,2	MCF-7	breast:
11	chr7:105110346..105111937-chr7:105127717..105129867,2	K562	blood:
12	chr7:105108727..105111208-chr7:105115281..105117815,3	K562	blood:
13	chr7:105093737..105097449-chr7:105099816..105103606,4	K562	blood:
14	chr7:105103366..105105752-chr7:105109309..105111791,2	K562	blood:
15	chr7:105108727..105111208-chr7:105115281..105117815,3	K562	blood:
16	chr7:105103366..105105752-chr7:105109309..105111791,2	K562	blood:
17	chr7:105090469..105092100-chr7:105095217..105096775,2	MCF-7	breast:
18	chr7:105039956..105042512-chr7:105104408..105106506,2	K562	blood:
19	chr7:104622804..104624627-chr7:105113661..105116251,2	K562	blood:
20	chr7:105094953..105097499-chr7:105172737..105175685,2	K562	blood:

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	PUS7	hsa-miR-155-5p	chr7:105097684-105097705
2	PUS7	hsa-miR-32-5p	chr7:105098074-105098095

Variant related genes	Relation type
PUS7	TF binding region
PUS7	CpG island
ENSG00000135250	chromatin interactions

Extended variants
information (count: 921 )
Associated
traits (count: 78 )

Variant overlapped rSNPs/rCNVs (count:921 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17148231	chr7:105094664-105094665	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs555338078	chr7:105094692-105094693	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs75484204	chr7:105094697-105094698	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs116290568	chr7:105094763-105094764	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs552756928	chr7:105094836-105094837	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs557785958	chr7:105094852-105094853	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs578141256	chr7:105094875-105094876	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs372619212	chr7:105094909-105094910	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs6972417	chr7:105094933-105094934	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs545912193	chr7:105094942-105094943	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs558194536	chr7:105094958-105094959	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs60616177	chr7:105095109-105095110	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs141787059	chr7:105095113-105095114	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs541884879	chr7:105095140-105095141	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs369366846	chr7:105095145-105095146	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs189024018	chr7:105095167-105095168	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs576390497	chr7:105095173-105095174	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs181084903	chr7:105095209-105095210	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs185615475	chr7:105095258-105095259	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs562288473	chr7:105095263-105095264	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs190701980	chr7:105095279-105095280	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs147086540	chr7:105095307-105095308	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs140002382	chr7:105095322-105095323	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs367587340	chr7:105095327-105095328	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs546456524	chr7:105095514-105095515	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs566804449	chr7:105095518-105095519	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs535376795	chr7:105095569-105095570	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs528080779	chr7:105095574-105095575	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs548825266	chr7:105095636-105095637	Weak transcription Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs75213304	chr7:105095637-105095638	Weak transcription Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs77404250	chr7:105095658-105095659	Weak transcription Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs76557474	chr7:105095659-105095660	Weak transcription Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs78774915	chr7:105095660-105095661	Weak transcription Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs75401442	chr7:105095661-105095662	Weak transcription Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs112216965	chr7:105095699-105095700	Weak transcription Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs11773001	chr7:105095708-105095709	Weak transcription Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs557847502	chr7:105095752-105095753	Weak transcription Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs529624900	chr7:105095797-105095798	Weak transcription Flanking Active TSS Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs578023829	chr7:105095800-105095801	Weak transcription Flanking Active TSS Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs546597484	chr7:105095803-105095804	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs375170094	chr7:105095804-105095805	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs10278911	chr7:105095815-105095816	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs554060926	chr7:105095830-105095831	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs138775322	chr7:105095835-105095836	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs557092767	chr7:105095878-105095879	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs543345203	chr7:105095879-105095880	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs563146466	chr7:105095882-105095883	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs575327479	chr7:105095897-105095898	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs544210511	chr7:105095904-105095905	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs59070916	chr7:105096001-105096002	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:78)

Disease	PMID	Source
Basal cell lymphoma	17170743	CNVD
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
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Non-small cell lung cancer	21829676	CNVD
Glioblastoma multiforme	17002787	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Lissencephaly	21572526	CNVD
Breast cancer	17603634	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	16397240	CNVD
Acute myeloid leukemia	16864856	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
small cell lung cancer	20016488	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
Metanephric adenoma	20802469	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
Malignant melanoma	17260012	CNVD
Myelodysplastic syndrome	21251322	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21785460	CNVD
Chronic myeloid leukemia	21384125	CNVD
Breast cancer	21858162	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Autism	19401682	CNVD
Neuroticism	17667963	CNVD
Prostate cancer	18632612	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	21364760	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	17053054	CNVD
Myelofibrosis	22110671	CNVD
Prostate cancer	16573809	CNVD
Pancreatic cancer	17952125	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:532 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:105080000-105108400	Weak transcription	Spleen	Spleen
2	chr7:105080000-105161200	Weak transcription	Pancreas	Pancrea
3	chr7:105080200-105104600	Weak transcription	Stomach Smooth Muscle	stomach
4	chr7:105080200-105126800	Weak transcription	Placenta Amnion	Placenta Amnion
5	chr7:105086800-105098200	Weak transcription	Ovary	ovary
6	chr7:105087200-105098200	Weak transcription	Fetal Stomach	stomach
7	chr7:105087200-105101400	Weak transcription	Left Ventricle	heart
8	chr7:105087200-105102000	Weak transcription	Aorta	Aorta
9	chr7:105088200-105099000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
10	chr7:105088200-105142600	Weak transcription	Esophagus	oesophagus
11	chr7:105088200-105152800	Weak transcription	Gastric	stomach
12	chr7:105088400-105097200	Weak transcription	Skeletal Muscle Female	skeletal muscle
13	chr7:105088400-105140400	Weak transcription	Rectal Mucosa Donor 29	rectum
14	chr7:105088800-105096200	Weak transcription	Dnd41	blood
15	chr7:105088800-105096600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr7:105089000-105096200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
17	chr7:105089000-105096600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
18	chr7:105089200-105127000	Weak transcription	Primary hematopoietic stem cells	blood
19	chr7:105089200-105142600	Weak transcription	Fetal Thymus	thymus
20	chr7:105089600-105145200	Weak transcription	Primary T helper cells fromperipheralblood	blood
21	chr7:105089600-105145800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
22	chr7:105090000-105126800	Weak transcription	Primary T cells fromperipheralblood	blood
23	chr7:105090000-105128200	Weak transcription	Primary T helper cells PMA-I stimulated	--
24	chr7:105090800-105102000	Weak transcription	GM12878-XiMat	blood
25	chr7:105090800-105120200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
26	chr7:105092000-105097600	Weak transcription	A549	lung
27	chr7:105092000-105097800	Weak transcription	Hela-S3	cervix
28	chr7:105092400-105095000	Enhancers	Primary B cells from cord blood	blood
29	chr7:105092600-105102000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
30	chr7:105092800-105096600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
31	chr7:105092800-105096600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
32	chr7:105092800-105098200	Weak transcription	Psoas Muscle	Psoas
33	chr7:105093000-105095400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
34	chr7:105093000-105096000	Enhancers	Primary neutrophils fromperipheralblood	blood
35	chr7:105093000-105096200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr7:105093200-105102000	Weak transcription	Primary T cells from cord blood	blood
37	chr7:105093200-105104400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
38	chr7:105093400-105112600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
39	chr7:105093600-105096200	Enhancers	HSMM	muscle
40	chr7:105093600-105097600	Weak transcription	Brain Germinal Matrix	brain
41	chr7:105093600-105101400	Weak transcription	H9 Cell Line	embryonic stem cell
42	chr7:105093600-105153000	Weak transcription	Small Intestine	intestine
43	chr7:105093800-105096000	Weak transcription	HUES64 Cell Line	embryonic stem cell
44	chr7:105093800-105102000	Weak transcription	Right Ventricle	heart
45	chr7:105094200-105094800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
46	chr7:105094200-105095000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
47	chr7:105094200-105095000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
48	chr7:105094200-105095000	Enhancers	Breast Myoepithelial Primary Cells	Breast
49	chr7:105094200-105095200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
50	chr7:105094200-105095600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin

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