Variant report

Variant	nsv1026851
Chromosome Location	chr7:27344799-27370551
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:123)
CpG islands
(count:61)
Chromatin interactive
region (count:8)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:123 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr7:27356062-27356334	IMR90	lung:	n/a	chr7:27356206-27356217
2	CEBPB	chr7:27356048-27356325	K562	blood:	n/a	chr7:27356206-27356217
3	CEBPB	chr7:27356068-27356324	Hela-S3	cervix:	n/a	chr7:27356206-27356217
4	CEBPB	chr7:27356132-27356232	H1-hESC	embryonic stem cell:	n/a	chr7:27356206-27356217
5	CEBPB	chr7:27356049-27356306	A549	lung:	n/a	chr7:27356206-27356217
6	CEBPB	chr7:27356026-27356323	HepG2	liver:	n/a	chr7:27356206-27356217
7	CTCF	chr7:27369720-27369870	HFF	foreskin:	n/a	n/a
8	CTCF	chr7:27369600-27369750	MCF-7	breast:	n/a	n/a
9	CTCF	chr7:27369707-27369741	LNCaP	prostate:	n/a	n/a
10	CTCF	chr7:27369800-27369950	GM12865	blood:	n/a	n/a
11	CTCF	chr7:27369680-27369830	GM12872	blood:	n/a	n/a
12	CTCF	chr7:27369700-27369850	HPF	lung:	n/a	n/a
13	CTCF	chr7:27369700-27369850	NHEK	skin:	n/a	n/a
14	CTCF	chr7:27369660-27369810	NB4	blood:	n/a	n/a
15	CTCF	chr7:27368240-27368390	GM12864	blood:	n/a	n/a
16	CTCF	chr7:27369680-27369830	HMF	breast:	n/a	n/a
17	CTCF	chr7:27369680-27369830	AG09309	skin:	n/a	n/a
18	CTCF	chr7:27369780-27369930	HepG2	liver:	n/a	n/a
19	CTCF	chr7:27369699-27369812	MCF-7	breast:	n/a	n/a
20	CTCF	chr7:27369720-27369870	A549	lung:	n/a	n/a
21	CTCF	chr7:27369600-27369750	BJ	skin:	n/a	n/a
22	CTCF	chr7:27369600-27369750	AG09309	skin:	n/a	n/a
23	CTCF	chr7:27369660-27369810	SK-N-SH_RA	brain:	n/a	n/a
24	CTCF	chr7:27369609-27369902	MCF-7	breast:	n/a	n/a
25	CTCF	chr7:27369640-27369790	Caco-2	colon:	n/a	n/a
26	CTCF	chr7:27369684-27369825	Hela-S3	cervix:	n/a	n/a
27	CTCF	chr7:27369660-27369810	HPF	lung:	n/a	n/a
28	CTCF	chr7:27369640-27369790	Hela-S3	cervix:	n/a	n/a
29	CTCF	chr7:27369660-27369810	SAEC	small airway:	n/a	n/a
30	CTCF	chr7:27369560-27369850	BE2_C	brain:	n/a	n/a
31	CTCF	chr7:27369700-27369850	AG04450	lung:	n/a	n/a
32	CTCF	chr7:27369619-27369862	A549	lung:	n/a	n/a
33	CTCF	chr7:27369660-27369810	HMF	breast:	n/a	n/a
34	CTCF	chr7:27369600-27369750	HCT-116	colon:	n/a	n/a
35	CTCF	chr7:27369680-27369830	HRPEpiC	eye:	n/a	n/a
36	CTCF	chr7:27369660-27369810	NHEK	skin:	n/a	n/a
37	CTCF	chr7:27369620-27369770	AG10803	skin:	n/a	n/a
38	CTCF	chr7:27369640-27369790	HRPEpiC	eye:	n/a	n/a
39	CTCF	chr7:27369620-27369770	HUVEC	blood vessel:	n/a	n/a
40	CTCF	chr7:27369621-27369888	H1-hESC	embryonic stem cell:	n/a	n/a
41	CTCF	chr7:27369660-27369810	HCPEpiC	choroid plexus:	n/a	n/a
42	CTCF	chr7:27369720-27369870	MCF-7	breast:	n/a	n/a
43	CTCF	chr7:27369640-27369790	HMEC	breast:	n/a	n/a
44	CTCF	chr7:27369760-27369910	HEEpiC	esophagus:	n/a	n/a
45	CTCF	chr7:27369760-27369910	GM12873	blood:	n/a	n/a
46	CTCF	chr7:27369680-27369830	NHDF-neo	bronchial:	n/a	n/a
47	CTCF	chr7:27369620-27369770	HCM	heart:	n/a	n/a
48	CTCF	chr7:27369660-27369810	HEK293	kidney:	n/a	n/a
49	CTCF	chr7:27369680-27369830	AoAF	blood vessel:	n/a	n/a
50	CTCF	chr7:27369720-27369870	NHLF	lung:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:27352954-27353004	HRE	kidney:	n/a
2	chr7:27352954-27353004	A549	lung:	n/a
3	chr7:27352954-27353004	PrEC	prostate:	n/a
4	chr7:27352954-27353004	HL-60	blood:	n/a
5	chr7:27352954-27353004	ovcar-3	ovarian:	n/a
6	chr7:27352954-27353004	BE2_C	brain:	n/a
7	chr7:27352954-27353004	HCT-116	colon:	n/a
8	chr7:27352954-27353004	AG04449	skin:	fetal
9	chr7:27352954-27353004	HCF	heart:	n/a
10	chr7:27352954-27353004	HEEpiC	esophagus:	n/a
11	chr7:27352954-27353004	HCPEpiC	choroid plexus:	n/a
12	chr7:27352954-27353004	MCF10A-Er-Src	breast:	n/a
13	chr7:27352954-27353004	AG10803	skin:	n/a
14	chr7:27352954-27353004	Hela-S3	cervix:	n/a
15	chr7:27352954-27353004	HepG2	liver:	n/a
16	chr7:27352954-27353004	HIPEpiC	eye:	n/a
17	chr7:27352954-27353004	NH-A	brain:	n/a
18	chr7:27352954-27353004	AG04450	lung:	fetal
19	chr7:27352954-27353004	HNPCEpiC	eye:	n/a
20	chr7:27352954-27353004	NHDF-neo	bronchial:	n/a
21	chr7:27352954-27353004	BJ	skin:	n/a
22	chr7:27352954-27353004	Caco-2	colon:	n/a
23	chr7:27352954-27353004	HEK293	kidney:	embryo
24	chr7:27352954-27353004	SK-N-SH	brain:	n/a
25	chr7:27352954-27353004	IMR90	lung:	fetal
26	chr7:27352954-27353004	Hepatocyte	liver:	n/a
27	chr7:27352954-27353004	PFSK-1	brain:	n/a
28	chr7:27352954-27353004	SK-N-MC	brain:	n/a
29	chr7:27352954-27353004	Jurkat	blood:	n/a
30	chr7:27352954-27353004	HRCEpiC	kidney:	n/a
31	chr7:27352954-27353004	K562	blood:	n/a
32	chr7:27352954-27353004	HCM	heart:	n/a
33	chr7:27352954-27353004	SK-N-SH_RA	brain:	n/a
34	chr7:27352954-27353004	LNCaP	prostate:	n/a
35	chr7:27352954-27353004	SAEC	small airway:	n/a
36	chr7:27352954-27353004	ProgFib	skin:	n/a
37	chr7:27352954-27353004	AoSMC	blood vessel:	n/a
38	chr7:27352954-27353004	AG09319	gingival:	n/a
39	chr7:27352954-27353004	HMEC	breast:	n/a
40	chr7:27352954-27353004	NB4	blood:	n/a
41	chr7:27352954-27353004	ECC-1	luminal epithelium:	n/a
42	chr7:27352954-27353004	GM12892	blood:	n/a
43	chr7:27352954-27353004	SKMC	muscle:	n/a
44	chr7:27352954-27353004	NHBE	bronchial:	n/a
45	chr7:27352954-27353004	CMK	blood:	n/a
46	chr7:27352954-27353004	GM19239	blood:	n/a
47	chr7:27352954-27353004	H1-hESC	embryonic stem cell:	embryo
48	chr7:27352954-27353004	MCF-7	breast:	n/a
49	chr7:27352954-27353004	HPAEpiC	pulmonary alveolar:	n/a
50	chr7:27352954-27353004	T-47D	breast:	n/a

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:27349970..27352592-chr7:27352932..27355272,3	K562	blood:
2	chr7:27353470..27355486-chr7:27620520..27622885,2	MCF-7	breast:
3	chr7:27349970..27352592-chr7:27352932..27355272,3	K562	blood:
4	chr7:27354696..27356208-chr7:27362416..27365005,2	MCF-7	breast:
5	chr7:27362143..27365035-chr7:27372640..27375053,2	MCF-7	breast:
6	7:27238414-27242313..7:27354053-27367655	Hela-S3	cervix:
7	chr7:27249672..27250374-chr7:27369354..27370262,2	MCF-7	breast:
8	chr7:27354696..27356208-chr7:27362416..27365005,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-EVX1-19	chr7:27367987-27368114	NONHSAT119729

No data

Variant related genes	Relation type
HNRNPA1P73	TF binding region
HNRNPA1P73	CpG island
ENSG00000243766	chromatin interactions
ENSG00000106031	chromatin interactions

Extended variants
information (count: 904 )
Associated
traits (count: 77 )

Variant overlapped rSNPs/rCNVs (count:904 , 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	rs6947275	chr7:27344799-27344800	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs573210056	chr7:27344828-27344829	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs371482761	chr7:27344835-27344836	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs540598494	chr7:27344872-27344873	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs565304087	chr7:27344895-27344896	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs6947692	chr7:27344905-27344906	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs551107169	chr7:27344930-27344931	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs563041653	chr7:27344944-27344945	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs111734605	chr7:27344983-27344984	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs17428638	chr7:27345020-27345021	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs572857536	chr7:27345140-27345141	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs367975928	chr7:27345162-27345163	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs548789557	chr7:27345206-27345207	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs535743233	chr7:27345214-27345215	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs567035142	chr7:27345250-27345251	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs545120198	chr7:27345261-27345262	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs187739033	chr7:27345283-27345284	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs546160321	chr7:27345284-27345285	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs555651255	chr7:27345286-27345287	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs570912760	chr7:27345355-27345356	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs146149860	chr7:27345500-27345501	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs574893676	chr7:27345514-27345515	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs556769833	chr7:27345524-27345525	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs375618850	chr7:27345531-27345532	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs191892434	chr7:27345541-27345542	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs536044231	chr7:27345583-27345584	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs554765177	chr7:27345595-27345596	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs573146843	chr7:27345617-27345618	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs140203954	chr7:27345666-27345667	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs565242008	chr7:27345731-27345732	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs551360883	chr7:27345732-27345733	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs578205245	chr7:27345773-27345774	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs370714740	chr7:27345774-27345775	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs372122491	chr7:27345776-27345777	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs35597781	chr7:27345784-27345785	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs17438278	chr7:27345785-27345786	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs34937897	chr7:27345864-27345865	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs142397383	chr7:27345959-27345960	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs7786428	chr7:27346031-27346032	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs17502538	chr7:27346035-27346036	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs368619935	chr7:27346068-27346069	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs150010937	chr7:27346078-27346079	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs17502545	chr7:27346093-27346094	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs557460361	chr7:27346119-27346120	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs563979280	chr7:27346121-27346122	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs189231107	chr7:27346142-27346143	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs549317538	chr7:27346159-27346160	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs17502552	chr7:27346216-27346217	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs570848420	chr7:27346218-27346219	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs531961105	chr7:27346219-27346220	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:77)

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
Pancreatic ductal adenocarcinoma	19077451	CNVD
Schizophrenia	23813976	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:51 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:27343000-27345000	Weak transcription	Skeletal Muscle Male	skeletal muscle
2	chr7:27344600-27344800	Enhancers	Psoas Muscle	Psoas
3	chr7:27344600-27346000	Enhancers	Skeletal Muscle Female	skeletal muscle
4	chr7:27344800-27345200	Weak transcription	Psoas Muscle	Psoas
5	chr7:27345000-27346400	Enhancers	Skeletal Muscle Male	skeletal muscle
6	chr7:27345200-27345800	Enhancers	Psoas Muscle	Psoas
7	chr7:27345400-27345600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr7:27345600-27346800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr7:27346800-27347200	Enhancers	Placenta Amnion	Placenta Amnion
10	chr7:27346800-27347600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr7:27347600-27352800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr7:27352200-27353400	Enhancers	ES-I3 Cell Line	embryonic stem cell
13	chr7:27352400-27353200	Enhancers	iPS-15b Cell Line	embryonic stem cell
14	chr7:27352400-27353200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
15	chr7:27352400-27353400	Enhancers	HUES48 Cell Line	embryonic stem cell
16	chr7:27352400-27353400	Enhancers	iPS-18 Cell Line	embryonic stem cell
17	chr7:27352400-27357000	Enhancers	Primary monocytes fromperipheralblood	blood
18	chr7:27352600-27353200	Enhancers	H9 Cell Line	embryonic stem cell
19	chr7:27352600-27353400	Enhancers	HUES6 Cell Line	embryonic stem cell
20	chr7:27352600-27353600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
21	chr7:27352600-27354400	Enhancers	iPS-20b Cell Line	embryonic stem cell
22	chr7:27352600-27355800	Enhancers	Monocytes-CD14+_RO01746	blood
23	chr7:27352800-27353200	Enhancers	HUES64 Cell Line	embryonic stem cell
24	chr7:27352800-27354400	Enhancers	H1 Cell Line	embryonic stem cell
25	chr7:27352800-27354600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
26	chr7:27353000-27353600	Enhancers	Placenta Amnion	Placenta Amnion
27	chr7:27353000-27354600	Enhancers	Placenta	Placenta
28	chr7:27353400-27356400	Enhancers	Fetal Lung	lung
29	chr7:27353600-27354000	Weak transcription	Placenta Amnion	Placenta Amnion
30	chr7:27353800-27354400	Enhancers	Primary hematopoietic stem cells short term culture	blood
31	chr7:27354000-27354800	Enhancers	Placenta Amnion	Placenta Amnion
32	chr7:27354000-27357400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
33	chr7:27354200-27354600	Enhancers	Adipose Nuclei	Adipose
34	chr7:27354200-27355000	Enhancers	Fetal Stomach	stomach
35	chr7:27354200-27357000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
36	chr7:27354400-27355800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
37	chr7:27354600-27355800	Weak transcription	Adipose Nuclei	Adipose
38	chr7:27354600-27356000	Weak transcription	Placenta	Placenta
39	chr7:27355800-27356200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
40	chr7:27355800-27356200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chr7:27355800-27356400	Enhancers	Primary hematopoietic stem cells short term culture	blood
42	chr7:27355800-27356400	Enhancers	Adipose Nuclei	Adipose
43	chr7:27355800-27356400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
44	chr7:27355800-27356600	Enhancers	Osteobl	bone
45	chr7:27356000-27356200	Enhancers	Placenta	Placenta
46	chr7:27356400-27356800	Enhancers	Monocytes-CD14+_RO01746	blood
47	chr7:27359800-27360000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
48	chr7:27360000-27361200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
49	chr7:27361200-27361800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
50	chr7:27363200-27364200	Enhancers	Primary monocytes fromperipheralblood	blood

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