Variant report

Variant	esv3504587
Chromosome Location	chr7:27782321-27784475
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:32)
CpG islands
(count:61)
Chromatin interactive
region (count:10)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:32 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:27784310-27784503	K562	blood:	n/a	n/a
2	CTCF	chr7:27784085-27785285	A549	lung:	n/a	chr7:27784884-27784905
3	CTCF	chr7:27784400-27784550	BJ	skin:	n/a	n/a
4	CTCF	chr7:27784392-27785235	HCT-116	colon:	n/a	chr7:27784884-27784905
5	CTCF	chr7:27784440-27784590	Caco-2	colon:	n/a	n/a
6	CTCF	chr7:27784449-27785284	SK-N-SH	brain:	n/a	chr7:27784884-27784905
7	CTCF	chr7:27784442-27785107	K562	blood:	n/a	chr7:27784884-27784905
8	EP300	chr7:27784457-27785180	A549	lung:	n/a	n/a
9	EP300	chr7:27782758-27783203	K562	blood:	n/a	chr7:27783099-27783107 chr7:27783189-27783203
10	EP300	chr7:27784316-27785045	K562	blood:	n/a	n/a
11	FOXA1	chr7:27784260-27784507	HepG2	liver:	n/a	chr7:27784444-27784456
12	FOXA1	chr7:27784162-27785102	HepG2	liver:	n/a	chr7:27784444-27784456
13	FOXA2	chr7:27784166-27784703	A549	lung:	n/a	chr7:27784444-27784456
14	FOXA2	chr7:27784278-27784476	HepG2	liver:	n/a	chr7:27784444-27784456
15	FOXA2	chr7:27784121-27784622	HepG2	liver:	n/a	chr7:27784444-27784456
16	GATA3	chr7:27784289-27784373	SH-SY5Y	brain:	n/a	n/a
17	MAFF	chr7:27782864-27782909	HepG2	liver:	n/a	n/a
18	MAFK	chr7:27782829-27782919	HepG2	liver:	n/a	chr7:27782877-27782892 chr7:27782877-27782888 chr7:27782877-27782893 chr7:27782876-27782890 chr7:27782877-27782888 chr7:27782878-27782889 chr7:27782878-27782889
19	MAFK	chr7:27782851-27782947	HepG2	liver:	n/a	chr7:27782877-27782892 chr7:27782877-27782888 chr7:27782877-27782893 chr7:27782876-27782890 chr7:27782877-27782888 chr7:27782878-27782889 chr7:27782878-27782889
20	MXI1	chr7:27784054-27785269	SK-N-SH	brain:	n/a	n/a
21	MYC	chr7:27784451-27785037	MCF10A-Er-Src	breast:	n/a	n/a
22	MYC	chr7:27782774-27783114	MCF10A-Er-Src	breast:	n/a	n/a
23	POLR2A	chr7:27784365-27785024	A549	lung:	n/a	n/a
24	POLR2A	chr7:27783002-27783076	HepG2	liver:	n/a	n/a
25	POLR2A	chr7:27784259-27785075	K562	blood:	n/a	n/a
26	RAD21	chr7:27784300-27785292	SK-N-SH	brain:	n/a	chr7:27784596-27784608
27	RAD21	chr7:27784445-27785235	HCT-116	colon:	n/a	chr7:27784596-27784608
28	SMC3	chr7:27784160-27785214	SK-N-SH	brain:	n/a	n/a
29	SP1	chr7:27784456-27785225	A549	lung:	n/a	n/a
30	STAT3	chr7:27784470-27784660	MCF10A-Er-Src	breast:	n/a	n/a
31	STAT3	chr7:27783178-27783325	MCF10A-Er-Src	breast:	n/a	n/a
32	TCF12	chr7:27784378-27785248	A549	lung:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:27782764-27782814	BE2_C	brain:	n/a
2	chr7:27782764-27782814	SKMC	muscle:	n/a
3	chr7:27782764-27782814	HRE	kidney:	n/a
4	chr7:27782764-27782814	GM19239	blood:	n/a
5	chr7:27782764-27782814	A549	lung:	n/a
6	chr7:27782764-27782814	HCT-116	colon:	n/a
7	chr7:27782764-27782814	IMR90	lung:	fetal
8	chr7:27782764-27782814	HPAEpiC	pulmonary alveolar:	n/a
9	chr7:27782764-27782814	MCF10A-Er-Src	breast:	n/a
10	chr7:27782764-27782814	AG10803	skin:	n/a
11	chr7:27782764-27782814	NT2-D1	testis:	n/a
12	chr7:27782764-27782814	HNPCEpiC	eye:	n/a
13	chr7:27782764-27782814	T-47D	breast:	n/a
14	chr7:27782764-27782814	K562	blood:	n/a
15	chr7:27782764-27782814	PrEC	prostate:	n/a
16	chr7:27782764-27782814	SK-N-SH_RA	brain:	n/a
17	chr7:27782764-27782814	PANC-1	pancreas:	n/a
18	chr7:27782764-27782814	AG04450	lung:	fetal
19	chr7:27782764-27782814	GM12878	blood:	n/a
20	chr7:27782764-27782814	GM06990	blood:	n/a
21	chr7:27782764-27782814	NH-A	brain:	n/a
22	chr7:27782764-27782814	SAEC	small airway:	n/a
23	chr7:27782764-27782814	HCM	heart:	n/a
24	chr7:27782764-27782814	MCF-7	breast:	n/a
25	chr7:27782764-27782814	CMK	blood:	n/a
26	chr7:27782764-27782814	HL-60	blood:	n/a
27	chr7:27782764-27782814	GM12891	blood:	n/a
28	chr7:27782764-27782814	NHDF-neo	bronchial:	n/a
29	chr7:27782764-27782814	RPTEC	kidney:	n/a
30	chr7:27782764-27782814	HIPEpiC	eye:	n/a
31	chr7:27782764-27782814	HCF	heart:	n/a
32	chr7:27782764-27782814	HEK293	kidney:	embryo
33	chr7:27782764-27782814	Hepatocyte	liver:	n/a
34	chr7:27782764-27782814	NHBE	bronchial:	n/a
35	chr7:27782764-27782814	Hela-S3	cervix:	n/a
36	chr7:27782764-27782814	LNCaP	prostate:	n/a
37	chr7:27782764-27782814	HUVEC	blood vessel:	n/a
38	chr7:27782764-27782814	HEEpiC	esophagus:	n/a
39	chr7:27782764-27782814	GM12892	blood:	n/a
40	chr7:27782764-27782814	NB4	blood:	n/a
41	chr7:27782764-27782814	AG09309	skin:	n/a
42	chr7:27782764-27782814	U87	brain:	n/a
43	chr7:27782764-27782814	PFSK-1	brain:	n/a
44	chr7:27782764-27782814	HepG2	liver:	n/a
45	chr7:27782764-27782814	ProgFib	skin:	n/a
46	chr7:27782764-27782814	HRCEpiC	kidney:	n/a
47	chr7:27782764-27782814	HAEpiC	amniotic membrane:	n/a
48	chr7:27782764-27782814	AoSMC	blood vessel:	n/a
49	chr7:27782764-27782814	H1-hESC	embryonic stem cell:	embryo
50	chr7:27782764-27782814	BJ	skin:	n/a

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:27777249..27781364-chr7:27781538..27788730,11	MCF-7	breast:
2	chr7:27699948..27706867-chr7:27775418..27784557,21	K562	blood:
3	chr7:27782398..27784453-chr7:27793755..27796214,2	K562	blood:
4	chr7:27783427..27786063-chr7:27789814..27792025,2	MCF-7	breast:
5	chr7:27777088..27781357-chr7:27783261..27787943,9	MCF-7	breast:
6	chr7:27702844..27705316-chr7:27782990..27784557,2	K562	blood:
7	chr7:27783237..27786573-chr7:27802443..27806955,4	K562	blood:
8	chr7:27700432..27708426-chr7:27777901..27782637,20	K562	blood:
9	chr7:27780417..27784283-chr7:27794073..27796581,3	MCF-7	breast:
10	chr7:27784235..27786861-chr7:27801505..27804201,3	K562	blood:

No data

Variant related genes	Relation type
ENSG00000229893	TF binding region
ENSG00000229893	CpG island
ENSG00000106052	chromatin interactions
ENSG00000106049	chromatin interactions
ENSG00000229893	chromatin interactions

Extended variants
information (count: 110 )
Associated
traits (count: 78 )

Variant overlapped rSNPs/rCNVs (count:110 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs113531761	chr7:27782336-27782337	Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs571637166	chr7:27782339-27782340	Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs368062908	chr7:27782340-27782341	Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs148579577	chr7:27782357-27782358	Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs553122595	chr7:27782370-27782371	Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs188235373	chr7:27782374-27782375	Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs553776795	chr7:27782377-27782378	Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs144143451	chr7:27782386-27782387	Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs573100475	chr7:27782424-27782425	Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs193001439	chr7:27782434-27782435	Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs576230795	chr7:27782488-27782489	Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs567498825	chr7:27782493-27782494	Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs147296570	chr7:27782502-27782503	Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs535996638	chr7:27782504-27782505	Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs555668818	chr7:27782550-27782551	Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs558593303	chr7:27782612-27782613	Weak transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs184352327	chr7:27782693-27782694	Weak transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs187243414	chr7:27782706-27782707	Weak transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs541437419	chr7:27782724-27782725	Weak transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs140930712	chr7:27782734-27782735	Weak transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs533147844	chr7:27782764-27782765	Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs374509276	chr7:27782765-27782766	Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs367781251	chr7:27782770-27782771	Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs192581421	chr7:27782798-27782799	Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs184615456	chr7:27782799-27782800	Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs17155744	chr7:27782800-27782801	Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs189298348	chr7:27782855-27782856	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs17685046	chr7:27782891-27782892	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
29	rs528735272	chr7:27782909-27782910	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs10230973	chr7:27782924-27782925	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
31	rs62449630	chr7:27782926-27782927	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs556433088	chr7:27782933-27782934	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs62449631	chr7:27783016-27783017	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
34	rs180853710	chr7:27783114-27783115	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs569634332	chr7:27783116-27783117	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs537265835	chr7:27783124-27783125	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs112901264	chr7:27783125-27783126	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs573881052	chr7:27783126-27783127	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs559853332	chr7:27783200-27783201	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs534642704	chr7:27783208-27783209	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs151279702	chr7:27783270-27783271	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs77739948	chr7:27783271-27783272	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs544986118	chr7:27783293-27783294	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs34943078	chr7:27783296-27783297	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs17685087	chr7:27783322-27783323	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs373437178	chr7:27783363-27783364	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs7810413	chr7:27783393-27783394	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs7810414	chr7:27783399-27783400	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs7810417	chr7:27783403-27783404	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs7810419	chr7:27783410-27783411	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:78)

Disease	PMID	Source
Urothelial carcinoma	18382360	CNVD
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Biliary cancer	19435499	CNVD
Cancer	16751803	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Wilms tumour	21544195	CNVD
Glioblastoma multiforme	17387387	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	18923191	CNVD
Glioma	21971842	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Oral cancer	21386901	CNVD
colon cancer	17210682	CNVD
Lung adenocarcinoma	21810691	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Colorectal cancer	19359472	CNVD
Hypothalamic hamartomas	18252217	CNVD
Human rectal carcinomas	16397240	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Medulloblastoma	18056178	CNVD
Basal cell lymphoma	17170743	CNVD
Ewing''s sarcoma	21437220	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	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
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Leukemia	23979775	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Autism	22495311	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Cancer	21637783	CNVD
Squamous cell cancer	20885788	CNVD
Breast cancer	16397240	CNVD
Non-small cell lung cancer	21829676	CNVD
Glioblastoma multiforme	17002787	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Glioblastoma multiforme	18628472	CNVD
Non-syndromic sensorineural hearing loss	22570644	CNVD
Cancer	21183584	CNVD
abnormal development	18461090	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	21785460	CNVD
Follicular lymphoma	20505157	CNVD
Williams-beuren syndrome	22470819	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Myelofibrosis	22110671	CNVD
Colorectal cancer	21645411	CNVD
Lung adenocarcinoma	17086460	CNVD
Colorectal cancer	19455253	CNVD
Lung cancer	17086460	CNVD
Cancer	17440070	CNVD
Breast cancer	22522925	CNVD
Lung adenocarcinoma	21935476	CNVD
Ovarian cancer	21781307	CNVD

Chromatin state (count:247 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:27780600-27784600	Weak transcription	Spleen	Spleen
2	chr7:27780800-27784600	Weak transcription	Left Ventricle	heart
3	chr7:27780800-27788800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr7:27780800-27789400	Weak transcription	Lung	lung
5	chr7:27780800-27796400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
6	chr7:27780800-27805600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr7:27780800-27810200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr7:27780800-27815200	Weak transcription	Gastric	stomach
9	chr7:27781000-27782400	Enhancers	Primary T cells fromperipheralblood	blood
10	chr7:27781000-27783200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
11	chr7:27781000-27784000	Weak transcription	HUVEC	blood vessel
12	chr7:27781000-27784200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
13	chr7:27781000-27784200	Weak transcription	NH-A	brain
14	chr7:27781000-27784400	Weak transcription	Cortex derived primary cultured neurospheres	brain
15	chr7:27781000-27784600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
16	chr7:27781000-27784600	Weak transcription	Brain Substantia Nigra	brain
17	chr7:27781000-27784600	Weak transcription	Colonic Mucosa	Colon
18	chr7:27781000-27784600	Weak transcription	Ovary	ovary
19	chr7:27781000-27789000	Weak transcription	Fetal Muscle Trunk	muscle
20	chr7:27781000-27800200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
21	chr7:27781000-27861800	Weak transcription	Aorta	Aorta
22	chr7:27781200-27782400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
23	chr7:27781200-27782400	Weak transcription	Fetal Intestine Small	intestine
24	chr7:27781200-27782400	Weak transcription	Pancreatic Islets	Pancreatic Islet
25	chr7:27781200-27782400	Weak transcription	Stomach Smooth Muscle	stomach
26	chr7:27781200-27782400	Weak transcription	A549	lung
27	chr7:27781200-27782800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
28	chr7:27781200-27783000	Enhancers	Primary neutrophils fromperipheralblood	blood
29	chr7:27781200-27783000	Enhancers	Primary T killer memory cells from peripheral blood	blood
30	chr7:27781200-27783200	Enhancers	Primary T helper naive cells from peripheral blood	blood
31	chr7:27781200-27784200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr7:27781200-27784200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
33	chr7:27781200-27784200	Weak transcription	Muscle Satellite Cultured Cells	--
34	chr7:27781200-27784200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
35	chr7:27781200-27784200	Weak transcription	Brain Inferior Temporal Lobe	brain
36	chr7:27781200-27784200	Weak transcription	Fetal Intestine Large	intestine
37	chr7:27781200-27784200	Weak transcription	Stomach Mucosa	stomach
38	chr7:27781200-27784200	Weak transcription	Dnd41	blood
39	chr7:27781200-27784200	Weak transcription	GM12878-XiMat	blood
40	chr7:27781200-27784200	Weak transcription	Hela-S3	cervix
41	chr7:27781200-27784200	Weak transcription	Osteobl	bone
42	chr7:27781200-27784400	Weak transcription	HUES64 Cell Line	embryonic stem cell
43	chr7:27781200-27784400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
44	chr7:27781200-27784400	Weak transcription	Primary T cells from cord blood	blood
45	chr7:27781200-27784400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
46	chr7:27781200-27784400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
47	chr7:27781200-27784400	Weak transcription	Placenta Amnion	Placenta Amnion
48	chr7:27781200-27784400	Weak transcription	HSMMtube	muscle
49	chr7:27781200-27784400	Weak transcription	NHLF	lung
50	chr7:27781200-27784600	Weak transcription	ES-I3 Cell Line	embryonic stem cell

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