Variant report

Variant	esv3450108
Chromosome Location	chr7:99339737-99383419
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:290)
CpG islands
(count:367)
Chromatin interactive
region (count:11)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:290 , 50 per page) page: 1 2 3 4 5 6

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	chr7:99370143-99370615	HepG2	liver:	n/a	n/a
4	ATF2	chr7:99365148-99365713	GM12878	blood:	n/a	n/a
5	ATF2	chr7:99365248-99365724	GM12878	blood:	n/a	n/a
6	BATF	chr7:99365247-99365623	GM12878	blood:	n/a	n/a
7	BATF	chr7:99365239-99365549	GM12878	blood:	n/a	n/a
8	BCL11A	chr7:99365231-99365629	GM12878	blood:	n/a	n/a
9	BHLHE40	chr7:99360674-99360886	K562	blood:	n/a	n/a
10	BHLHE40	chr7:99366245-99366383	GM12878	blood:	n/a	n/a
11	BHLHE40	chr7:99365355-99365633	GM12878	blood:	n/a	n/a
12	BRCA1	chr7:99349579-99349590	Hela-S3	cervix:	n/a	n/a
13	CBX3	chr7:99360292-99360970	K562	blood:	n/a	n/a
14	CEBPB	chr7:99370271-99370552	HepG2	liver:	n/a	n/a
15	CEBPB	chr7:99354445-99354721	HepG2	liver:	n/a	chr7:99354587-99354598 chr7:99354587-99354600 chr7:99354589-99354600
16	CEBPB	chr7:99370297-99370473	HepG2	liver:	n/a	n/a
17	CEBPB	chr7:99360356-99360612	K562	blood:	n/a	n/a
18	CEBPB	chr7:99354505-99354705	IMR90	lung:	n/a	chr7:99354587-99354598 chr7:99354587-99354600 chr7:99354589-99354600
19	CEBPB	chr7:99354480-99354737	A549	lung:	n/a	chr7:99354587-99354598 chr7:99354587-99354600 chr7:99354589-99354600
20	CEBPB	chr7:99340773-99340954	HepG2	liver:	n/a	n/a
21	CEBPB	chr7:99354474-99354734	K562	blood:	n/a	chr7:99354587-99354598 chr7:99354587-99354600 chr7:99354589-99354600
22	CHD2	chr7:99365347-99365565	GM12878	blood:	n/a	n/a
23	CTCF	chr7:99379980-99380130	K562	blood:	n/a	n/a
24	CTCF	chr7:99379920-99380070	RPTEC	kidney:	n/a	n/a
25	CTCF	chr7:99379940-99380090	HMEC	breast:	n/a	n/a
26	CTCF	chr7:99379940-99380090	HepG2	liver:	n/a	n/a
27	CTCF	chr7:99349224-99349264	Kidney_OC	kidney:	n/a	n/a
28	CTCF	chr7:99379946-99380130	K562	blood:	n/a	n/a
29	CTCF	chr7:99379926-99380103	HepG2	liver:	n/a	n/a
30	CTCF	chr7:99379900-99380050	GM12872	blood:	n/a	n/a
31	CTCF	chr7:99380023-99380072	Hela-S3	cervix:	n/a	n/a
32	CTCF	chr7:99379520-99379670	GM12869	blood:	n/a	n/a
33	CTCF	chr7:99380003-99380091	HepG2	liver:	n/a	n/a
34	CTCF	chr7:99379960-99380110	HEK293	kidney:	n/a	n/a
35	CTCF	chr7:99379904-99380157	K562	blood:	n/a	n/a
36	CTCF	chr7:99379980-99380130	MCF-7	breast:	n/a	n/a
37	CUX1	chr7:99360597-99361175	K562	blood:	n/a	n/a
38	CUX1	chr7:99358092-99358259	K562	blood:	n/a	n/a
39	CUX1	chr7:99365256-99365588	GM12878	blood:	n/a	n/a
40	EBF1	chr7:99365230-99365634	GM12878	blood:	n/a	chr7:99365456-99365467
41	EBF1	chr7:99360832-99361020	GM12878	blood:	n/a	n/a
42	EBF1	chr7:99365165-99365749	GM12878	blood:	n/a	chr7:99365456-99365467
43	EBF1	chr7:99365268-99365651	GM12878	blood:	n/a	chr7:99365456-99365467
44	EBF1	chr7:99361696-99361858	GM12878	blood:	n/a	n/a
45	ELF1	chr7:99370237-99370540	HepG2	liver:	n/a	n/a
46	ELK1	chr7:99365390-99365532	GM12878	blood:	n/a	n/a
47	EP300	chr7:99365290-99365561	GM12878	blood:	n/a	n/a
48	EP300	chr7:99340119-99340757	HepG2	liver:	n/a	n/a
49	EP300	chr7:99364259-99364654	Hela-S3	cervix:	n/a	n/a
50	EP300	chr7:99350249-99350293	K562	blood:	n/a	n/a

(count:367 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:99376495-99376545	Hepatocyte	liver:	n/a
2	chr7:99376495-99376545	Hepatocyte	liver:	n/a
3	chr7:99376495-99376545	Caco-2	colon:	n/a
4	chr7:99355204-99355254	H1-hESC	embryonic stem cell:	embryo
5	chr7:99383224-99383274	GM06990	blood:	n/a
6	chr7:99383224-99383274	IMR90	lung:	fetal
7	chr7:99382086-99382136	LNCaP	prostate:	n/a
8	chr7:99383224-99383274	CMK	blood:	n/a
9	chr7:99382086-99382136	AoSMC	blood vessel:	n/a
10	chr7:99382086-99382136	SK-N-SH_RA	brain:	n/a
11	chr7:99382086-99382136	HUVEC	blood vessel:	n/a
12	chr7:99383224-99383274	H1-hESC	embryonic stem cell:	embryo
13	chr7:99355204-99355254	U87	brain:	n/a
14	chr7:99376495-99376545	GM12892	blood:	n/a
15	chr7:99382086-99382136	ProgFib	skin:	n/a
16	chr7:99376495-99376545	SKMC	muscle:	n/a
17	chr7:99383155-99383205	HCPEpiC	choroid plexus:	n/a
18	chr7:99382086-99382136	AG04450	lung:	fetal
19	chr7:99355204-99355254	HPAEpiC	pulmonary alveolar:	n/a
20	chr7:99382086-99382136	HAEpiC	amniotic membrane:	n/a
21	chr7:99383224-99383274	GM12892	blood:	n/a
22	chr7:99382370-99382420	NB4	blood:	n/a
23	chr7:99376495-99376545	K562	blood:	n/a
24	chr7:99382086-99382136	K562	blood:	n/a
25	chr7:99382086-99382136	NH-A	brain:	n/a
26	chr7:99383224-99383274	SK-N-MC	brain:	n/a
27	chr7:99355204-99355254	HCF	heart:	n/a
28	chr7:99376495-99376545	PANC-1	pancreas:	n/a
29	chr7:99382370-99382420	Hepatocyte	liver:	n/a
30	chr7:99382370-99382420	ProgFib	skin:	n/a
31	chr7:99355204-99355254	RPTEC	kidney:	n/a
32	chr7:99355204-99355254	Hepatocyte	liver:	n/a
33	chr7:99376495-99376545	HEK293	kidney:	embryo
34	chr7:99383224-99383274	RPTEC	kidney:	n/a
35	chr7:99382086-99382136	MCF-7	breast:	n/a
36	chr7:99376495-99376545	U87	brain:	n/a
37	chr7:99376495-99376545	HRCEpiC	kidney:	n/a
38	chr7:99376495-99376545	GM12891	blood:	n/a
39	chr7:99355204-99355254	ProgFib	skin:	n/a
40	chr7:99355204-99355254	BE2_C	brain:	n/a
41	chr7:99383155-99383205	AG09309	skin:	n/a
42	chr7:99382370-99382420	NHBE	bronchial:	n/a
43	chr7:99382370-99382420	SK-N-SH	brain:	n/a
44	chr7:99376495-99376545	HL-60	blood:	n/a
45	chr7:99383155-99383205	PFSK-1	brain:	n/a
46	chr7:99383155-99383205	A549	lung:	n/a
47	chr7:99383155-99383205	H1-hESC	embryonic stem cell:	embryo
48	chr7:99383224-99383274	HPAEpiC	pulmonary alveolar:	n/a
49	chr7:99382370-99382420	HRPEpiC	eye:	n/a
50	chr7:99383155-99383205	RPTEC	kidney:	n/a

(count:11 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:99355786..99358236-chr7:99360607..99362683,2	K562	blood:
2	chr7:99348892..99351554-chr7:99353145..99355344,2	MCF-7	breast:
3	chr7:99374500..99377711-chr7:99378798..99381871,3	MCF-7	breast:
4	chr7:99358230..99360940-chr7:99460072..99462897,2	K562	blood:
5	chr7:99374500..99377711-chr7:99378798..99381871,3	MCF-7	breast:
6	chr7:99341182..99342708-chr7:99343739..99346587,2	MCF-7	breast:
7	chr7:99355786..99358236-chr7:99360607..99362683,2	K562	blood:
8	chr7:99348892..99351554-chr7:99353145..99355344,2	MCF-7	breast:
9	chr7:99213903..99216853-chr7:99350391..99352771,2	K562	blood:
10	chr7:99364077..99366983-chr7:99367660..99369579,3	K562	blood:
11	chr7:99341182..99342708-chr7:99343739..99346587,2	MCF-7	breast:

(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
CYP3A4	CpG island
ENSG00000273407	CpG island
ENSG00000197037	chromatin interactions
ENSG00000160868	chromatin interactions
ENSG00000273407	chromatin interactions

Extended variants
information (count: 1618 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:1618 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs111987843	chr7:99339738-99339739	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs145972743	chr7:99339750-99339751	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs145551381	chr7:99339752-99339753	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs535422950	chr7:99339759-99339760	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs2741872	chr7:99339776-99339777	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs184098389	chr7:99339821-99339822	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs370992368	chr7:99339825-99339826	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs539158497	chr7:99339828-99339829	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs557898676	chr7:99339835-99339836	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs55883246	chr7:99339844-99339845	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs148907422	chr7:99339852-99339853	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs543751465	chr7:99339885-99339886	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs540456651	chr7:99339936-99339937	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs556013440	chr7:99339938-99339939	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs143595079	chr7:99339946-99339947	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs544546138	chr7:99339947-99339948	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs367978627	chr7:99339980-99339981	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs2741871	chr7:99340048-99340049	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs12538820	chr7:99340049-99340050	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	mRNA abundance
20	rs112424553	chr7:99340104-99340105	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs76798941	chr7:99340134-99340135	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs560596505	chr7:99340168-99340169	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs528280372	chr7:99340191-99340192	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs148094588	chr7:99340258-99340259	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs939955	chr7:99340259-99340260	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs539083365	chr7:99340300-99340301	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs34702057	chr7:99340352-99340353	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs189840530	chr7:99340368-99340369	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs550511557	chr7:99340386-99340387	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs182247009	chr7:99340439-99340440	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs372217391	chr7:99340510-99340511	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs557196236	chr7:99340540-99340541	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs186897123	chr7:99340595-99340596	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs191690041	chr7:99340638-99340639	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs372611866	chr7:99340650-99340651	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs78183855	chr7:99340651-99340652	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs369989862	chr7:99340675-99340676	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs528135395	chr7:99340752-99340753	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs566268196	chr7:99340768-99340769	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs184197545	chr7:99340778-99340779	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs555682534	chr7:99340810-99340811	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs373453158	chr7:99340827-99340828	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs377263376	chr7:99340843-99340844	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs375468680	chr7:99340845-99340846	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs578055477	chr7:99340869-99340870	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs368220858	chr7:99340896-99340897	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs370950517	chr7:99340929-99340930	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs545433816	chr7:99340959-99340960	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs79239470	chr7:99340979-99340980	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs536428300	chr7:99341054-99341055	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:297 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:99306800-99340800	Weak transcription	Brain Cingulate Gyrus	brain
2	chr7:99311800-99349000	Weak transcription	Duodenum Smooth Muscle	Duodenum
3	chr7:99334800-99340800	Weak transcription	Pancreas	Pancrea
4	chr7:99335800-99340000	Weak transcription	Brain Hippocampus Middle	brain
5	chr7:99335800-99340600	Weak transcription	Brain Inferior Temporal Lobe	brain
6	chr7:99337000-99341800	Enhancers	HepG2	liver
7	chr7:99337200-99339800	Enhancers	Skeletal Muscle Female	skeletal muscle
8	chr7:99337600-99339800	Enhancers	HSMMtube	muscle
9	chr7:99337600-99341000	Enhancers	Fetal Muscle Leg	muscle
10	chr7:99337800-99340800	Weak transcription	Brain Angular Gyrus	brain
11	chr7:99338400-99339800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
12	chr7:99338800-99341000	Enhancers	Liver	Liver
13	chr7:99339000-99339800	Weak transcription	Hela-S3	cervix
14	chr7:99339200-99346400	Weak transcription	Aorta	Aorta
15	chr7:99339200-99352200	Weak transcription	Left Ventricle	heart
16	chr7:99339400-99340400	Weak transcription	Psoas Muscle	Psoas
17	chr7:99339800-99340000	Enhancers	Hela-S3	cervix
18	chr7:99339800-99341200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
19	chr7:99340000-99346600	Weak transcription	Hela-S3	cervix
20	chr7:99340400-99340600	Enhancers	Psoas Muscle	Psoas
21	chr7:99340800-99341000	Enhancers	Pancreas	Pancrea
22	chr7:99341000-99348000	Weak transcription	Pancreas	Pancrea
23	chr7:99341800-99345200	Weak transcription	HepG2	liver
24	chr7:99345200-99345800	Enhancers	HepG2	liver
25	chr7:99345600-99345800	Enhancers	Small Intestine	intestine
26	chr7:99345800-99348200	Weak transcription	HepG2	liver
27	chr7:99346000-99346800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
28	chr7:99346000-99347400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
29	chr7:99346200-99350200	Enhancers	Placenta Amnion	Placenta Amnion
30	chr7:99346400-99346800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr7:99346400-99350400	Enhancers	HMEC	breast
32	chr7:99346600-99347400	Enhancers	Hela-S3	cervix
33	chr7:99346600-99350200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
34	chr7:99346600-99350200	Enhancers	NHEK	skin
35	chr7:99346600-99350400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
36	chr7:99346800-99347000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
37	chr7:99346800-99350000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr7:99347400-99347800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
39	chr7:99347400-99347800	Weak transcription	Hela-S3	cervix
40	chr7:99347400-99348600	Enhancers	Esophagus	oesophagus
41	chr7:99347600-99348200	Weak transcription	Aorta	Aorta
42	chr7:99347800-99349000	Enhancers	Hela-S3	cervix
43	chr7:99347800-99350400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
44	chr7:99348000-99348200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
45	chr7:99348000-99348600	Bivalent Enhancer	H9 Derived Neuron Cultured Cells	ES cell derived
46	chr7:99348000-99348600	Enhancers	Pancreas	Pancrea
47	chr7:99348000-99348600	Enhancers	Rectal Smooth Muscle	rectum
48	chr7:99348000-99348600	Enhancers	Skeletal Muscle Female	skeletal muscle
49	chr7:99348000-99349000	Enhancers	A549	lung
50	chr7:99348000-99350800	Enhancers	Fetal Intestine Small	intestine

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