Variant report

Variant	esv3331003
Chromosome Location	chr7:99337054-99386069
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:332)
CpG islands
(count:366)
Chromatin interactive
region (count:14)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:332 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:99364310-99364654	K562	blood:	n/a	n/a
2	ARID3A	chr7:99339924-99340664	HepG2	liver:	n/a	n/a
3	ARID3A	chr7:99338418-99338613	HepG2	liver:	n/a	n/a
4	ARID3A	chr7:99370143-99370615	HepG2	liver:	n/a	n/a
5	ATF2	chr7:99365248-99365724	GM12878	blood:	n/a	n/a
6	ATF2	chr7:99365148-99365713	GM12878	blood:	n/a	n/a
7	BATF	chr7:99365239-99365549	GM12878	blood:	n/a	n/a
8	BATF	chr7:99365247-99365623	GM12878	blood:	n/a	n/a
9	BCL11A	chr7:99365231-99365629	GM12878	blood:	n/a	n/a
10	BHLHE40	chr7:99360674-99360886	K562	blood:	n/a	n/a
11	BHLHE40	chr7:99365355-99365633	GM12878	blood:	n/a	n/a
12	BHLHE40	chr7:99366245-99366383	GM12878	blood:	n/a	n/a
13	BRCA1	chr7:99349579-99349590	Hela-S3	cervix:	n/a	n/a
14	CBX3	chr7:99360292-99360970	K562	blood:	n/a	n/a
15	CEBPB	chr7:99338408-99338693	HepG2	liver:	n/a	chr7:99338505-99338516
16	CEBPB	chr7:99337482-99337652	H1-hESC	embryonic stem cell:	n/a	n/a
17	CEBPB	chr7:99340773-99340954	HepG2	liver:	n/a	n/a
18	CEBPB	chr7:99354480-99354737	A549	lung:	n/a	chr7:99354587-99354598 chr7:99354587-99354600 chr7:99354589-99354600
19	CEBPB	chr7:99354505-99354705	IMR90	lung:	n/a	chr7:99354587-99354598 chr7:99354587-99354600 chr7:99354589-99354600
20	CEBPB	chr7:99360356-99360612	K562	blood:	n/a	n/a
21	CEBPB	chr7:99338034-99338599	IMR90	lung:	n/a	chr7:99338505-99338516
22	CEBPB	chr7:99354474-99354734	K562	blood:	n/a	chr7:99354587-99354598 chr7:99354587-99354600 chr7:99354589-99354600
23	CEBPB	chr7:99338412-99338612	A549	lung:	n/a	chr7:99338505-99338516
24	CEBPB	chr7:99337522-99337834	HepG2	liver:	n/a	chr7:99337779-99337792
25	CEBPB	chr7:99370297-99370473	HepG2	liver:	n/a	n/a
26	CEBPB	chr7:99354445-99354721	HepG2	liver:	n/a	chr7:99354587-99354598 chr7:99354587-99354600 chr7:99354589-99354600
27	CEBPB	chr7:99370271-99370552	HepG2	liver:	n/a	n/a
28	CEBPB	chr7:99337749-99338785	Hela-S3	cervix:	n/a	chr7:99337779-99337792 chr7:99338505-99338516
29	CHD2	chr7:99365347-99365565	GM12878	blood:	n/a	n/a
30	CTCF	chr7:99379940-99380090	HepG2	liver:	n/a	n/a
31	CTCF	chr7:99379920-99380070	RPTEC	kidney:	n/a	n/a
32	CTCF	chr7:99379520-99379670	GM12869	blood:	n/a	n/a
33	CTCF	chr7:99379904-99380157	K562	blood:	n/a	n/a
34	CTCF	chr7:99349224-99349264	Kidney_OC	kidney:	n/a	n/a
35	CTCF	chr7:99380003-99380091	HepG2	liver:	n/a	n/a
36	CTCF	chr7:99337740-99337890	HMEC	breast:	n/a	n/a
37	CTCF	chr7:99379900-99380050	GM12872	blood:	n/a	n/a
38	CTCF	chr7:99379960-99380110	HEK293	kidney:	n/a	n/a
39	CTCF	chr7:99337860-99338010	SAEC	small airway:	n/a	n/a
40	CTCF	chr7:99379980-99380130	MCF-7	breast:	n/a	n/a
41	CTCF	chr7:99379980-99380130	K562	blood:	n/a	n/a
42	CTCF	chr7:99379946-99380130	K562	blood:	n/a	n/a
43	CTCF	chr7:99339435-99339459	LNCaP	prostate:	n/a	n/a
44	CTCF	chr7:99379926-99380103	HepG2	liver:	n/a	n/a
45	CTCF	chr7:99380023-99380072	Hela-S3	cervix:	n/a	n/a
46	CTCF	chr7:99379940-99380090	HMEC	breast:	n/a	n/a
47	CTCF	chr7:99337860-99338010	HMF	breast:	n/a	n/a
48	CUX1	chr7:99358092-99358259	K562	blood:	n/a	n/a
49	CUX1	chr7:99360597-99361175	K562	blood:	n/a	n/a
50	CUX1	chr7:99365256-99365588	GM12878	blood:	n/a	n/a

(count:366 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:99383224-99383274	HCF	heart:	n/a
2	chr7:99376495-99376545	AG04449	skin:	fetal
3	chr7:99383224-99383274	HPAEpiC	pulmonary alveolar:	n/a
4	chr7:99382086-99382136	HRPEpiC	eye:	n/a
5	chr7:99376495-99376545	PFSK-1	brain:	n/a
6	chr7:99383155-99383205	A549	lung:	n/a
7	chr7:99382086-99382136	NB4	blood:	n/a
8	chr7:99383224-99383274	HEK293	kidney:	embryo
9	chr7:99383224-99383274	NT2-D1	testis:	n/a
10	chr7:99383155-99383205	PANC-1	pancreas:	n/a
11	chr7:99383155-99383205	HCF	heart:	n/a
12	chr7:99382370-99382420	Jurkat	blood:	n/a
13	chr7:99382370-99382420	IMR90	lung:	fetal
14	chr7:99355204-99355254	HEEpiC	esophagus:	n/a
15	chr7:99382086-99382136	AG10803	skin:	n/a
16	chr7:99382370-99382420	Caco-2	colon:	n/a
17	chr7:99383155-99383205	HAEpiC	amniotic membrane:	n/a
18	chr7:99383155-99383205	AG09319	gingival:	n/a
19	chr7:99383224-99383274	RPTEC	kidney:	n/a
20	chr7:99382370-99382420	SK-N-SH_RA	brain:	n/a
21	chr7:99376495-99376545	HMEC	breast:	n/a
22	chr7:99382370-99382420	AG04450	lung:	fetal
23	chr7:99383155-99383205	AG04449	skin:	fetal
24	chr7:99376495-99376545	SK-N-SH	brain:	n/a
25	chr7:99376495-99376545	CMK	blood:	n/a
26	chr7:99355204-99355254	HCT-116	colon:	n/a
27	chr7:99383224-99383274	Hepatocyte	liver:	n/a
28	chr7:99376495-99376545	K562	blood:	n/a
29	chr7:99355204-99355254	U87	brain:	n/a
30	chr7:99383224-99383274	HUVEC	blood vessel:	n/a
31	chr7:99383224-99383274	HCM	heart:	n/a
32	chr7:99382370-99382420	HMEC	breast:	n/a
33	chr7:99383224-99383274	SAEC	small airway:	n/a
34	chr7:99383155-99383205	BJ	skin:	n/a
35	chr7:99382370-99382420	PrEC	prostate:	n/a
36	chr7:99376495-99376545	HEK293	kidney:	embryo
37	chr7:99383155-99383205	LNCaP	prostate:	n/a
38	chr7:99355204-99355254	HNPCEpiC	eye:	n/a
39	chr7:99376495-99376545	AG09309	skin:	n/a
40	chr7:99382086-99382136	AG09319	gingival:	n/a
41	chr7:99355204-99355254	HRE	kidney:	n/a
42	chr7:99382086-99382136	IMR90	lung:	fetal
43	chr7:99376495-99376545	ProgFib	skin:	n/a
44	chr7:99382086-99382136	GM06990	blood:	n/a
45	chr7:99355204-99355254	BJ	skin:	n/a
46	chr7:99382370-99382420	HRPEpiC	eye:	n/a
47	chr7:99383155-99383205	ECC-1	luminal epithelium:	n/a
48	chr7:99355204-99355254	A549	lung:	n/a
49	chr7:99383224-99383274	BE2_C	brain:	n/a
50	chr7:99383224-99383274	Caco-2	colon:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr7:99348892..99351554-chr7:99353145..99355344,2	MCF-7	breast:
2	chr7:99331906..99334521-chr7:99334977..99338227,4	MCF-7	breast:
3	chr7:99355786..99358236-chr7:99360607..99362683,2	K562	blood:
4	chr7:99374500..99377711-chr7:99378798..99381871,3	MCF-7	breast:
5	chr7:99364077..99366983-chr7:99367660..99369579,3	K562	blood:
6	chr7:99341182..99342708-chr7:99343739..99346587,2	MCF-7	breast:
7	chr7:99213903..99216853-chr7:99350391..99352771,2	K562	blood:
8	chr7:99355786..99358236-chr7:99360607..99362683,2	K562	blood:
9	chr7:99358230..99360940-chr7:99460072..99462897,2	K562	blood:
10	chr7:99380939..99382491-chr7:99384838..99386622,2	K562	blood:
11	chr7:99374500..99377711-chr7:99378798..99381871,3	MCF-7	breast:
12	chr7:99341182..99342708-chr7:99343739..99346587,2	MCF-7	breast:
13	chr7:99348892..99351554-chr7:99353145..99355344,2	MCF-7	breast:
14	chr7:99327792..99330076-chr7:99335753..99337453,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CYP3A43-6	chr7:99364166-99364515	ENSG00000273407.1

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	CYP3A4	hsa-miR-27b-3p	chr7:99355142-99355162

Variant related genes	Relation type
CYP3A4	TF binding region
ENSG00000273407	TF binding region
CYP3A7	TF binding region
CYP3A4	CpG island
ENSG00000273407	CpG island
CYP3A7	CpG island
ENSG00000160870	chromatin interactions
ENSG00000160868	chromatin interactions
ENSG00000197037	chromatin interactions
ENSG00000273407	chromatin interactions

Extended variants
information (count: 1812 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:1812 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs548803486	chr7:99337059-99337060	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs570248974	chr7:99337065-99337066	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs531238091	chr7:99337079-99337080	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs138917228	chr7:99337118-99337119	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs141303115	chr7:99337132-99337133	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs184407499	chr7:99337138-99337139	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs2980374	chr7:99337243-99337244	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs368942381	chr7:99337251-99337252	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs150408738	chr7:99337265-99337266	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs72494456	chr7:99337272-99337273	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs554797839	chr7:99337356-99337357	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs576214104	chr7:99337378-99337379	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs376517883	chr7:99337392-99337393	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs138123702	chr7:99337405-99337406	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs374972998	chr7:99337408-99337409	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs539567615	chr7:99337458-99337459	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs149597665	chr7:99337497-99337498	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs559149652	chr7:99337512-99337513	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs190441726	chr7:99337556-99337557	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs541059651	chr7:99337669-99337670	Enhancers Weak transcription Flanking Active TSS Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs146085203	chr7:99337677-99337678	Enhancers Weak transcription Flanking Active TSS Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs140155549	chr7:99337781-99337782	Enhancers Weak transcription Flanking Active TSS Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs370743116	chr7:99337797-99337798	Enhancers Weak transcription Flanking Active TSS Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs375080537	chr7:99337804-99337805	Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs542010015	chr7:99337830-99337831	Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs182159064	chr7:99337866-99337867	Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs531077532	chr7:99337872-99337873	Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs552855693	chr7:99337876-99337877	Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs564468502	chr7:99337966-99337967	Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs575776532	chr7:99337995-99337996	Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs528454051	chr7:99338007-99338008	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs528310678	chr7:99338048-99338049	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs546631503	chr7:99338104-99338105	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs568213209	chr7:99338106-99338107	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs184433121	chr7:99338107-99338108	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs548042913	chr7:99338147-99338148	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs2687127	chr7:99338188-99338189	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs536874117	chr7:99338231-99338232	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs189284433	chr7:99338232-99338233	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs2222410	chr7:99338358-99338359	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs577248906	chr7:99338384-99338385	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs370607957	chr7:99338577-99338578	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs534595384	chr7:99338591-99338592	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs571529223	chr7:99338637-99338638	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs59172435	chr7:99338650-99338651	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs181206531	chr7:99338684-99338685	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs142136536	chr7:99338685-99338686	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs115021352	chr7:99338688-99338689	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs573613245	chr7:99338707-99338708	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs546022806	chr7:99338712-99338713	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:95)

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
Stenocardia	21860640	CNVD
Vasospasm	21860640	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
Gastric cancer	24379144	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
Prostate cancer	16461572	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
Bladder cancer	21909424	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Biliary cancer	19435499	CNVD
Myelofibrosis	22110671	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	16608533	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Liver carcinoma	19366792	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Adenocarcinoma	19607727	CNVD
Multiple myeloma	16461302	CNVD
Breast cancer	21858162	CNVD
Emphysema	19352772	CNVD
Effusion lymphoma	18079361	CNVD
Medulloblastoma	17653508	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Autism	19401682	CNVD
Neuroticism	17667963	CNVD
Breast cancer	21509527	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Prostate cancer	18632612	CNVD
Urothelial carcinoma	21177765	CNVD
Cancer	20164919	CNVD
Congenital diaphragmatic hernia	21525063	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
T-cell lymphomas	22341440	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:392 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:99303200-99337200	Weak transcription	Skeletal Muscle Female	skeletal muscle
2	chr7:99306000-99339000	Weak transcription	Stomach Smooth Muscle	stomach
3	chr7:99306800-99340800	Weak transcription	Brain Cingulate Gyrus	brain
4	chr7:99311800-99349000	Weak transcription	Duodenum Smooth Muscle	Duodenum
5	chr7:99320000-99337200	Weak transcription	Brain Angular Gyrus	brain
6	chr7:99321800-99338200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
7	chr7:99324400-99339200	Weak transcription	Brain Substantia Nigra	brain
8	chr7:99327200-99339200	Weak transcription	Brain Anterior Caudate	brain
9	chr7:99331200-99337600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr7:99331400-99338800	Weak transcription	Liver	Liver
11	chr7:99333600-99339600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr7:99334400-99337600	Weak transcription	Skeletal Muscle Male	skeletal muscle
13	chr7:99334400-99337800	Strong transcription	Left Ventricle	heart
14	chr7:99334600-99338800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr7:99334800-99340800	Weak transcription	Pancreas	Pancrea
16	chr7:99335000-99337800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
17	chr7:99335600-99337600	Weak transcription	HSMMtube	muscle
18	chr7:99335800-99337600	Weak transcription	HSMM	muscle
19	chr7:99335800-99338400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
20	chr7:99335800-99338400	Weak transcription	Adipose Nuclei	Adipose
21	chr7:99335800-99340000	Weak transcription	Brain Hippocampus Middle	brain
22	chr7:99335800-99340600	Weak transcription	Brain Inferior Temporal Lobe	brain
23	chr7:99336000-99337200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
24	chr7:99336000-99337400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
25	chr7:99336400-99337800	Strong transcription	Aorta	Aorta
26	chr7:99336600-99337600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
27	chr7:99336600-99338400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
28	chr7:99336800-99337200	Weak transcription	NHEK	skin
29	chr7:99336800-99337600	Weak transcription	Lung	lung
30	chr7:99336800-99339000	Weak transcription	Psoas Muscle	Psoas
31	chr7:99337000-99337400	Weak transcription	HMEC	breast
32	chr7:99337000-99337600	Enhancers	iPS-15b Cell Line	embryonic stem cell
33	chr7:99337000-99341800	Enhancers	HepG2	liver
34	chr7:99337200-99337800	Strong transcription	Brain Angular Gyrus	brain
35	chr7:99337200-99338400	Enhancers	NHEK	skin
36	chr7:99337200-99339200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
37	chr7:99337200-99339800	Enhancers	Skeletal Muscle Female	skeletal muscle
38	chr7:99337400-99337600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
39	chr7:99337400-99337800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
40	chr7:99337400-99338000	Enhancers	HMEC	breast
41	chr7:99337600-99337800	Enhancers	ES-I3 Cell Line	embryonic stem cell
42	chr7:99337600-99337800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
43	chr7:99337600-99338000	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
44	chr7:99337600-99338400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
45	chr7:99337600-99338400	Enhancers	Monocytes-CD14+_RO01746	blood
46	chr7:99337600-99339000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
47	chr7:99337600-99339000	Enhancers	Hela-S3	cervix
48	chr7:99337600-99339200	Enhancers	HSMM	muscle
49	chr7:99337600-99339400	Enhancers	Primary monocytes fromperipheralblood	blood
50	chr7:99337600-99339400	Enhancers	Primary neutrophils fromperipheralblood	blood

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