Variant report

Variant	esv2761325
Chromosome Location	chr7:48409639-48557382
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr7:48454339-48454412	K562	blood:	n/a	n/a
2	ATF1	chr7:48464645-48464750	K562	blood:	n/a	n/a
3	BATF	chr7:48483391-48483642	GM12878	blood:	n/a	n/a
4	BCL3	chr7:48537205-48537464	GM12878	blood:	n/a	n/a
5	BHLHE40	chr7:48430530-48430791	GM12878	blood:	n/a	n/a
6	BHLHE40	chr7:48495321-48495335	K562	blood:	n/a	n/a
7	CCNT2	chr7:48470894-48471088	K562	blood:	n/a	n/a
8	CCNT2	chr7:48494647-48495097	K562	blood:	n/a	n/a
9	CEBPB	chr7:48456901-48457130	Hela-S3	cervix:	n/a	n/a
10	CEBPB	chr7:48473077-48473360	A549	lung:	n/a	chr7:48473193-48473204
11	CEBPB	chr7:48498727-48499141	MCF-7	breast:	n/a	chr7:48498891-48498904
12	CEBPB	chr7:48473078-48473360	HepG2	liver:	n/a	chr7:48473193-48473204
13	CEBPB	chr7:48456467-48456702	HepG2	liver:	n/a	chr7:48456564-48456577 chr7:48456564-48456575
14	CEBPB	chr7:48428785-48428793	H1-hESC	embryonic stem cell:	n/a	n/a
15	CEBPB	chr7:48545497-48545781	IMR90	lung:	n/a	chr7:48545643-48545654
16	CEBPB	chr7:48545495-48545834	HepG2	liver:	n/a	chr7:48545643-48545654
17	CEBPB	chr7:48466497-48466781	MCF-7	breast:	n/a	chr7:48466632-48466643
18	CEBPB	chr7:48500485-48500804	HepG2	liver:	n/a	chr7:48500623-48500634
19	CEBPB	chr7:48473100-48473293	K562	blood:	n/a	chr7:48473193-48473204
20	CEBPB	chr7:48542623-48542856	H1-hESC	embryonic stem cell:	n/a	n/a
21	CEBPB	chr7:48501342-48501446	HepG2	liver:	n/a	n/a
22	CEBPB	chr7:48546971-48547149	HepG2	liver:	n/a	chr7:48547003-48547014 chr7:48547001-48547012 chr7:48547003-48547014 chr7:48547001-48547014
23	CEBPB	chr7:48498813-48499028	HepG2	liver:	n/a	chr7:48498891-48498904
24	CEBPB	chr7:48429601-48429900	MCF-7	breast:	n/a	n/a
25	CEBPB	chr7:48473131-48473331	Hela-S3	cervix:	n/a	chr7:48473193-48473204
26	CEBPB	chr7:48500568-48500665	A549	lung:	n/a	chr7:48500623-48500634
27	CEBPB	chr7:48429446-48429963	MCF-7	breast:	n/a	n/a
28	CEBPB	chr7:48545578-48545826	A549	lung:	n/a	chr7:48545643-48545654
29	CEBPB	chr7:48429541-48429870	IMR90	lung:	n/a	n/a
30	CEBPB	chr7:48498754-48499043	Hela-S3	cervix:	n/a	chr7:48498891-48498904
31	CEBPB	chr7:48510603-48510792	H1-hESC	embryonic stem cell:	n/a	chr7:48510656-48510667 chr7:48510656-48510665 chr7:48510654-48510665
32	CEBPB	chr7:48510492-48510812	K562	blood:	n/a	chr7:48510656-48510667 chr7:48510656-48510665 chr7:48510654-48510665
33	CEBPB	chr7:48473031-48473381	IMR90	lung:	n/a	chr7:48473193-48473204
34	CEBPB	chr7:48498776-48499010	A549	lung:	n/a	chr7:48498891-48498904
35	CEBPB	chr7:48531253-48531488	HepG2	liver:	n/a	chr7:48531357-48531368 chr7:48531357-48531370
36	CEBPB	chr7:48510500-48510740	A549	lung:	n/a	chr7:48510656-48510667 chr7:48510656-48510665 chr7:48510654-48510665
37	CEBPB	chr7:48498646-48499135	MCF-7	breast:	n/a	chr7:48498891-48498904
38	CEBPB	chr7:48510520-48510805	HepG2	liver:	n/a	chr7:48510656-48510667 chr7:48510656-48510665 chr7:48510654-48510665
39	CHD2	chr7:48501565-48501582	HepG2	liver:	n/a	n/a
40	CTCF	chr7:48483502-48483573	LNCaP	prostate:	n/a	n/a
41	CTCF	chr7:48464431-48464695	NHEK	skin:	n/a	chr7:48464560-48464581 chr7:48464558-48464576
42	CTCF	chr7:48464520-48464670	GM12865	blood:	n/a	chr7:48464560-48464581 chr7:48464558-48464576
43	CTCF	chr7:48464480-48464630	AG04449	skin:	n/a	chr7:48464560-48464581 chr7:48464558-48464576
44	CTCF	chr7:48423939-48424041	A549	lung:	n/a	n/a
45	CTCF	chr7:48423974-48424049	MCF-7	breast:	n/a	n/a
46	CTCF	chr7:48464480-48464630	HVMF	connective:	n/a	chr7:48464560-48464581 chr7:48464558-48464576
47	CTCF	chr7:48464460-48464610	NHDF-neo	bronchial:	n/a	chr7:48464560-48464581 chr7:48464558-48464576
48	CTCF	chr7:48483556-48483597	GM13977	blood:	n/a	n/a
49	CTCF	chr7:48464460-48464610	WERI-Rb-1	eye:	n/a	chr7:48464560-48464581 chr7:48464558-48464576
50	CTCF	chr7:48494579-48494630	Gliobla	brain:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:48495157-48495207	HRCEpiC	kidney:	n/a
2	chr7:48494608-48494658	SKMC	muscle:	n/a
3	chr7:48494362-48494412	SAEC	small airway:	n/a
4	chr7:48552817-48552867	MCF10A-Er-Src	breast:	n/a
5	chr7:48495157-48495207	HRCEpiC	kidney:	n/a
6	chr7:48494608-48494658	SKMC	muscle:	n/a
7	chr7:48494362-48494412	SAEC	small airway:	n/a
8	chr7:48552817-48552867	MCF10A-Er-Src	breast:	n/a
9	chr7:48494156-48494206	GM19239	blood:	n/a
10	chr7:48494519-48494569	MCF-7	breast:	n/a
11	chr7:48494519-48494569	H1-hESC	embryonic stem cell:	embryo
12	chr7:48494579-48494629	NHBE	bronchial:	n/a
13	chr7:48491590-48491640	ECC-1	luminal epithelium:	n/a
14	chr7:48495215-48495265	HAEpiC	amniotic membrane:	n/a
15	chr7:48495333-48495383	ovcar-3	ovarian:	n/a
16	chr7:48495333-48495383	HAEpiC	amniotic membrane:	n/a
17	chr7:48495157-48495207	BE2_C	brain:	n/a
18	chr7:48494519-48494569	GM12892	blood:	n/a
19	chr7:48552817-48552867	HepG2	liver:	n/a
20	chr7:48494156-48494206	RPTEC	kidney:	n/a
21	chr7:48494362-48494412	H1-hESC	embryonic stem cell:	embryo
22	chr7:48552817-48552867	HPAEpiC	pulmonary alveolar:	n/a
23	chr7:48491590-48491640	GM06990	blood:	n/a
24	chr7:48495072-48495122	PrEC	prostate:	n/a
25	chr7:48494734-48494784	HCPEpiC	choroid plexus:	n/a
26	chr7:48494362-48494412	HCT-116	colon:	n/a
27	chr7:48552817-48552867	HEEpiC	esophagus:	n/a
28	chr7:48495215-48495265	SAEC	small airway:	n/a
29	chr7:48495157-48495207	SK-N-MC	brain:	n/a
30	chr7:48494608-48494658	HL-60	blood:	n/a
31	chr7:48494156-48494206	IMR90	lung:	fetal
32	chr7:48494362-48494412	ProgFib	skin:	n/a
33	chr7:48495215-48495265	HCM	heart:	n/a
34	chr7:48495157-48495207	NHBE	bronchial:	n/a
35	chr7:48493792-48493842	U87	brain:	n/a
36	chr7:48494579-48494629	MCF10A-Er-Src	breast:	n/a
37	chr7:48495333-48495383	NHDF-neo	bronchial:	n/a
38	chr7:48491590-48491640	SK-N-SH_RA	brain:	n/a
39	chr7:48495215-48495265	IMR90	lung:	fetal
40	chr7:48494734-48494784	LNCaP	prostate:	n/a
41	chr7:48495072-48495122	CMK	blood:	n/a
42	chr7:48495333-48495383	HEK293	kidney:	embryo
43	chr7:48494608-48494658	AG09319	gingival:	n/a
44	chr7:48552817-48552867	HCM	heart:	n/a
45	chr7:48495072-48495122	SKMC	muscle:	n/a
46	chr7:48493792-48493842	HEK293	kidney:	embryo
47	chr7:48494156-48494206	PrEC	prostate:	n/a
48	chr7:48494734-48494784	GM19239	blood:	n/a
49	chr7:48495072-48495122	HCT-116	colon:	n/a
50	chr7:48495215-48495265	ECC-1	luminal epithelium:	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:48513865..48515812-chr7:49402658..49405453,2	K562	blood:
2	chr7:48464131..48464720-chr7:49830437..49831304,2	MCF-7	breast:
3	chr7:48464162..48465007-chr7:49040934..49041504,2	MCF-7	breast:
4	chr7:48546224..48548443-chr7:48555422..48558329,2	MCF-7	breast:
5	chr7:48464147..48465026-chr7:48914660..48915807,4	MCF-7	breast:
6	chr7:48464066..48464994-chr7:48914675..48915561,3	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SUN3-5	chr7:48491789-48495224	NONHSAT120528

Variant related genes	Relation type
ABCA13	TF binding region
ABCA13	CpG island
ENSG00000179869	chromatin interactions

Extended variants
information (count: 5639 )
Associated
traits (count: 124 )

Variant overlapped rSNPs/rCNVs (count:5639 , 50 per page) page: 1 2 3 4 5 6 7 ... 113

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2117089	chr7:48409639-48409640	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs534536294	chr7:48409669-48409670	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs554751380	chr7:48409673-48409674	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs574918029	chr7:48409704-48409705	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs35286333	chr7:48409705-48409706	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs12534760	chr7:48409709-48409710	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs113839444	chr7:48409781-48409782	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs183841473	chr7:48409795-48409796	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs189156948	chr7:48409805-48409806	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs546488694	chr7:48409823-48409824	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs35784364	chr7:48409845-48409846	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs192842898	chr7:48409868-48409869	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs149708440	chr7:48409902-48409903	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs542474927	chr7:48409917-48409918	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs532484337	chr7:48409942-48409943	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs557549676	chr7:48409968-48409969	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs560809489	chr7:48410017-48410018	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs115436241	chr7:48410026-48410027	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs565748064	chr7:48410054-48410055	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs549612612	chr7:48410092-48410093	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs563254454	chr7:48410111-48410112	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs76642884	chr7:48410129-48410130	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs562271224	chr7:48410136-48410137	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs184586938	chr7:48410141-48410142	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs374191827	chr7:48410159-48410160	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs145566267	chr7:48410171-48410172	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs561958013	chr7:48410172-48410173	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs548414331	chr7:48410187-48410188	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs187007171	chr7:48410206-48410207	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs537514776	chr7:48410246-48410247	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs191787847	chr7:48410261-48410262	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs577279606	chr7:48410301-48410302	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs573957254	chr7:48410328-48410329	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs73099316	chr7:48410329-48410330	ZNF genes & repeats Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs141197629	chr7:48410352-48410353	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs573617572	chr7:48410433-48410434	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs184334164	chr7:48410512-48410513	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs562261029	chr7:48410535-48410536	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs146960647	chr7:48410544-48410545	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs111730077	chr7:48410613-48410614	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs539207618	chr7:48410618-48410619	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs181029710	chr7:48410632-48410633	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs147597164	chr7:48410668-48410669	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs551796871	chr7:48410714-48410715	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs559220455	chr7:48410747-48410748	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs528324585	chr7:48410781-48410782	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs201840021	chr7:48410870-48410871	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs548199517	chr7:48410877-48410878	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs185471568	chr7:48410909-48410910	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs536873931	chr7:48410934-48410935	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:124)

Disease	PMID	Source
Glioblastoma multiforme	17387387	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Biliary cancer	19435499	CNVD
Wilms tumour	21544195	CNVD
Neuroblastoma	18923191	CNVD
Glioma	21971842	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Medulloblastoma	21979893	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
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Lung cancer	18438408	CNVD
lymphocytic leukemia	21291569	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Cancer	21637783	CNVD
Squamous cell cancer	20885788	CNVD
Breast cancer	16397240	CNVD
Non-small cell lung cancer	21829676	CNVD
Glioblastoma multiforme	17002787	CNVD
Autism	22495311	CNVD
Glioblastoma multiforme	18628472	CNVD
Cancer	21183584	CNVD
Breast cancer	21785460	CNVD
Follicular lymphoma	20505157	CNVD
Williams-beuren syndrome	22470819	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	21364760	CNVD
Acute myeloid leukemia	21251322	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Multiple myeloma	16461302	CNVD
Glioblastoma multiforme	21750150	CNVD
Hepatocellular carcinoma	16750200	CNVD
Acute myeloid leukemia	17237825	CNVD
Gastric cancer	24379144	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Abnormal phenotypes	18644119	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Esophageal cancer	21851588	CNVD
Lung adenocarcinoma	17086460	CNVD
Lung cancer	17086460	CNVD
Non-small cell lung cancer	17643093	CNVD
Ovarian cancer	18182111	CNVD
Colorectal cancer	16272173	CNVD
Glioblastoma multiforme	17369134	CNVD
Barrett''s esophagus	18559552	CNVD
head and neck squamous cell carcinoma	16943533	CNVD
Anaplastic thyroid cancer	17079354	CNVD
Basal-like breast cancer	17875215	CNVD
Colorectal cancer	16882699	CNVD
Colorectal cancer	18794099	CNVD
Gastrointestinal stromal cancer	17643098	CNVD
Lung cancer	18381415	CNVD
Metastatic colorectal cancer	17664472	CNVD
Non-small cell lung cancer	19255323	CNVD
Non-small cell lung cancer	17673923	CNVD
Non-small cell lung cancer	17975165	CNVD
Non-small cell lung cancer	19622585	CNVD
Ovarian cancer	16607561	CNVD
Squamous cell cancer	19670535	CNVD
head and neck squamous cell carcinoma	16818711	CNVD
small cell lung cancer	18829487	CNVD
Breast cancer	17661082	CNVD
Adenocarcinoma	19260752	CNVD
Esophageal cancer	16575012	CNVD
Lung adenocarcinoma	19138956	CNVD
Lung adenocarcinoma	18379350	CNVD
Lung adenocarcinoma	18258923	CNVD
Lung cancer	19138956	CNVD
Lung cancer	18379350	CNVD
Lung cancer	18258923	CNVD
Non-small cell lung cancer	18304967	CNVD
Non-small cell lung cancer	19451690	CNVD
Non-small cell lung cancer	19260752	CNVD
Non-small cell lung cancer	17079354	CNVD
Non-small cell lung cancer	18559607	CNVD
Rectal cancer	19506820	CNVD
Triple-negative breast cancer	18950515	CNVD
head and neck squamous cell carcinoma	18813952	CNVD
Non-small cell lung cancer	17504988	CNVD
Non-small cell lung cancer	16943533	CNVD
Non-small cell lung cancer	18509184	CNVD
head and neck squamous cell carcinoma	17538160	CNVD
Colorectal cancer	19712476	CNVD
Lung adenocarcinoma	19525976	CNVD
Lung cancer	19525976	CNVD
Lung cancer	19671679	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
small cell lung cancer	20016488	CNVD
Myelofibrosis	22110671	CNVD
Lissencephaly	21572526	CNVD
Breast cancer	17603634	CNVD
Acute myeloid leukemia	16864856	CNVD
Pancreatic cancer	17952125	CNVD
Colorectal cancer	21645411	CNVD
Breast cancer	22522925	CNVD
Schizophrenia	23813976	CNVD

Chromatin state (count:428 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:48406400-48410200	Strong transcription	Primary hematopoietic stem cells	blood
2	chr7:48406600-48410200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr7:48409200-48410000	Weak transcription	Primary neutrophils fromperipheralblood	blood
4	chr7:48410000-48410200	Strong transcription	Primary neutrophils fromperipheralblood	blood
5	chr7:48410200-48410400	Weak transcription	Primary neutrophils fromperipheralblood	blood
6	chr7:48410200-48410600	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr7:48410200-48411600	Weak transcription	Primary hematopoietic stem cells	blood
8	chr7:48410400-48410600	Strong transcription	Primary neutrophils fromperipheralblood	blood
9	chr7:48410600-48410800	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr7:48410600-48411800	Weak transcription	Primary neutrophils fromperipheralblood	blood
11	chr7:48410800-48411400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr7:48411000-48427200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr7:48411400-48411800	Enhancers	Primary monocytes fromperipheralblood	blood
14	chr7:48411400-48413200	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr7:48411600-48412000	Strong transcription	Primary hematopoietic stem cells	blood
16	chr7:48411600-48414600	Enhancers	Breast Myoepithelial Primary Cells	Breast
17	chr7:48411800-48418600	Strong transcription	Primary neutrophils fromperipheralblood	blood
18	chr7:48411800-48420400	Weak transcription	Primary monocytes fromperipheralblood	blood
19	chr7:48412000-48414000	Weak transcription	Primary hematopoietic stem cells	blood
20	chr7:48413200-48413600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
21	chr7:48413200-48432600	Weak transcription	Spleen	Spleen
22	chr7:48413600-48414400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
23	chr7:48413800-48414600	Enhancers	HMEC	breast
24	chr7:48414000-48414400	Enhancers	NHEK	skin
25	chr7:48414000-48414600	Strong transcription	Primary hematopoietic stem cells	blood
26	chr7:48414000-48414600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
27	chr7:48414000-48414600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
28	chr7:48414200-48414600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
29	chr7:48414400-48423600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
30	chr7:48414600-48417800	Weak transcription	Primary hematopoietic stem cells	blood
31	chr7:48415800-48416800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr7:48417800-48418400	Strong transcription	Primary hematopoietic stem cells	blood
33	chr7:48418400-48422400	Weak transcription	Primary hematopoietic stem cells	blood
34	chr7:48418600-48420000	Weak transcription	Primary neutrophils fromperipheralblood	blood
35	chr7:48420000-48424800	Strong transcription	Primary neutrophils fromperipheralblood	blood
36	chr7:48420400-48420800	Enhancers	Primary monocytes fromperipheralblood	blood
37	chr7:48420400-48420800	Enhancers	Monocytes-CD14+_RO01746	blood
38	chr7:48420400-48421800	Enhancers	Fetal Brain Female	brain
39	chr7:48420600-48421200	Enhancers	Fetal Brain Male	brain
40	chr7:48421200-48422000	Enhancers	Brain Germinal Matrix	brain
41	chr7:48421800-48422600	Weak transcription	Fetal Brain Female	brain
42	chr7:48422400-48424400	Strong transcription	Primary hematopoietic stem cells	blood
43	chr7:48422600-48422800	Enhancers	Fetal Brain Female	brain
44	chr7:48423400-48424400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
45	chr7:48423600-48424200	Enhancers	HMEC	breast
46	chr7:48423600-48424400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
47	chr7:48423600-48424400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
48	chr7:48424200-48429000	Weak transcription	HMEC	breast
49	chr7:48424400-48428600	Weak transcription	Primary hematopoietic stem cells	blood
50	chr7:48424400-48429400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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