Variant report

Variant	nsv817336
Chromosome Location	chr7:48238233-48563988
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1700)
CpG islands
(count:1038)
Chromatin interactive
region (count:16)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1700 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:48240766-48240966	K562	blood:	n/a	n/a
2	ATF1	chr7:48464645-48464750	K562	blood:	n/a	n/a
3	ATF1	chr7:48454339-48454412	K562	blood:	n/a	n/a
4	ATF2	chr7:48291310-48291832	GM12878	blood:	n/a	n/a
5	ATF2	chr7:48285619-48286161	GM12878	blood:	n/a	n/a
6	ATF2	chr7:48294644-48295012	GM12878	blood:	n/a	n/a
7	ATF2	chr7:48291293-48291808	GM12878	blood:	n/a	n/a
8	ATF2	chr7:48338313-48338712	GM12878	blood:	n/a	n/a
9	ATF2	chr7:48338249-48338768	GM12878	blood:	n/a	n/a
10	BACH1	chr7:48271579-48271852	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr7:48240792-48240874	H1-hESC	embryonic stem cell:	n/a	n/a
12	BATF	chr7:48291362-48291801	GM12878	blood:	n/a	n/a
13	BATF	chr7:48285668-48286127	GM12878	blood:	n/a	n/a
14	BATF	chr7:48291306-48291870	GM12878	blood:	n/a	n/a
15	BATF	chr7:48285785-48286103	GM12878	blood:	n/a	n/a
16	BATF	chr7:48338311-48338717	GM12878	blood:	n/a	n/a
17	BATF	chr7:48294654-48294978	GM12878	blood:	n/a	n/a
18	BATF	chr7:48294726-48294922	GM12878	blood:	n/a	n/a
19	BATF	chr7:48483391-48483642	GM12878	blood:	n/a	n/a
20	BCL11A	chr7:48294690-48294938	GM12878	blood:	n/a	n/a
21	BCL11A	chr7:48291390-48291765	GM12878	blood:	n/a	n/a
22	BCL11A	chr7:48338302-48338688	GM12878	blood:	n/a	n/a
23	BCL11A	chr7:48285709-48286092	GM12878	blood:	n/a	n/a
24	BCL3	chr7:48338337-48338739	GM12878	blood:	n/a	n/a
25	BCL3	chr7:48400134-48400508	GM12878	blood:	n/a	n/a
26	BCL3	chr7:48400193-48400497	GM12878	blood:	n/a	n/a
27	BCL3	chr7:48537205-48537464	GM12878	blood:	n/a	n/a
28	BCL3	chr7:48285640-48286075	GM12878	blood:	n/a	n/a
29	BCL3	chr7:48291391-48291682	GM12878	blood:	n/a	n/a
30	BCL3	chr7:48294619-48294966	GM12878	blood:	n/a	n/a
31	BCLAF1	chr7:48291285-48291674	GM12878	blood:	n/a	n/a
32	BHLHE40	chr7:48495321-48495335	K562	blood:	n/a	n/a
33	BHLHE40	chr7:48298658-48298686	GM12878	blood:	n/a	n/a
34	BHLHE40	chr7:48294391-48294424	GM12878	blood:	n/a	n/a
35	BHLHE40	chr7:48291414-48291704	GM12878	blood:	n/a	n/a
36	BHLHE40	chr7:48430530-48430791	GM12878	blood:	n/a	n/a
37	BRCA1	chr7:48354292-48354447	GM12878	blood:	n/a	n/a
38	CCNT2	chr7:48494647-48495097	K562	blood:	n/a	n/a
39	CCNT2	chr7:48470894-48471088	K562	blood:	n/a	n/a
40	CEBPB	chr7:48531253-48531488	HepG2	liver:	n/a	chr7:48531357-48531368 chr7:48531357-48531370
41	CEBPB	chr7:48318208-48318512	A549	lung:	n/a	n/a
42	CEBPB	chr7:48466497-48466781	MCF-7	breast:	n/a	chr7:48466632-48466643
43	CEBPB	chr7:48498754-48499043	Hela-S3	cervix:	n/a	chr7:48498891-48498904
44	CEBPB	chr7:48318199-48318505	HepG2	liver:	n/a	n/a
45	CEBPB	chr7:48350535-48350812	HepG2	liver:	n/a	chr7:48350667-48350680 chr7:48350667-48350678
46	CEBPB	chr7:48473131-48473331	Hela-S3	cervix:	n/a	chr7:48473193-48473204
47	CEBPB	chr7:48429601-48429900	MCF-7	breast:	n/a	n/a
48	CEBPB	chr7:48429446-48429963	MCF-7	breast:	n/a	n/a
49	CEBPB	chr7:48510603-48510792	H1-hESC	embryonic stem cell:	n/a	chr7:48510656-48510667 chr7:48510656-48510665 chr7:48510654-48510665
50	CEBPB	chr7:48252008-48252228	A549	lung:	n/a	chr7:48252125-48252136

(count:1038 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:48495157-48495207	ovcar-3	ovarian:	n/a
2	chr7:48495157-48495207	ovcar-3	ovarian:	n/a
3	chr7:48494734-48494784	Caco-2	colon:	n/a
4	chr7:48352531-48352581	A549	lung:	n/a
5	chr7:48493792-48493842	SAEC	small airway:	n/a
6	chr7:48495333-48495383	HRPEpiC	eye:	n/a
7	chr7:48319696-48319746	Hepatocyte	liver:	n/a
8	chr7:48494519-48494569	LNCaP	prostate:	n/a
9	chr7:48319696-48319746	AG10803	skin:	n/a
10	chr7:48495157-48495207	RPTEC	kidney:	n/a
11	chr7:48495072-48495122	T-47D	breast:	n/a
12	chr7:48552817-48552867	SK-N-MC	brain:	n/a
13	chr7:48494734-48494784	GM12892	blood:	n/a
14	chr7:48495333-48495383	HCPEpiC	choroid plexus:	n/a
15	chr7:48552817-48552867	SK-N-SH	brain:	n/a
16	chr7:48493792-48493842	SK-N-MC	brain:	n/a
17	chr7:48494519-48494569	Hela-S3	cervix:	n/a
18	chr7:48494579-48494629	HNPCEpiC	eye:	n/a
19	chr7:48495215-48495265	NB4	blood:	n/a
20	chr7:48494156-48494206	PrEC	prostate:	n/a
21	chr7:48352531-48352581	PFSK-1	brain:	n/a
22	chr7:48319696-48319746	NT2-D1	testis:	n/a
23	chr7:48493792-48493842	ECC-1	luminal epithelium:	n/a
24	chr7:48494608-48494658	LNCaP	prostate:	n/a
25	chr7:48494156-48494206	ovcar-3	ovarian:	n/a
26	chr7:48491590-48491640	HPAEpiC	pulmonary alveolar:	n/a
27	chr7:48351495-48351545	HMEC	breast:	n/a
28	chr7:48319696-48319746	AG09319	gingival:	n/a
29	chr7:48493792-48493842	PANC-1	pancreas:	n/a
30	chr7:48495215-48495265	AoSMC	blood vessel:	n/a
31	chr7:48495215-48495265	PANC-1	pancreas:	n/a
32	chr7:48494734-48494784	HRCEpiC	kidney:	n/a
33	chr7:48491590-48491640	BJ	skin:	n/a
34	chr7:48552817-48552867	ECC-1	luminal epithelium:	n/a
35	chr7:48494362-48494412	HEK293	kidney:	embryo
36	chr7:48494519-48494569	HEK293	kidney:	embryo
37	chr7:48494519-48494569	PANC-1	pancreas:	n/a
38	chr7:48495157-48495207	NT2-D1	testis:	n/a
39	chr7:48494519-48494569	HCT-116	colon:	n/a
40	chr7:48494362-48494412	NHBE	bronchial:	n/a
41	chr7:48495215-48495265	AG04449	skin:	fetal
42	chr7:48495072-48495122	PrEC	prostate:	n/a
43	chr7:48494734-48494784	T-47D	breast:	n/a
44	chr7:48494608-48494658	ProgFib	skin:	n/a
45	chr7:48494362-48494412	ProgFib	skin:	n/a
46	chr7:48494362-48494412	H1-hESC	embryonic stem cell:	embryo
47	chr7:48495333-48495383	H1-hESC	embryonic stem cell:	embryo
48	chr7:48351495-48351545	SK-N-MC	brain:	n/a
49	chr7:48319696-48319746	T-47D	breast:	n/a
50	chr7:48494734-48494784	HCF	heart:	n/a

(count:16 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:48464162..48465007-chr7:49040934..49041504,2	MCF-7	breast:
2	chr7:48546224..48548443-chr7:48555422..48558329,2	MCF-7	breast:
3	chr7:48513865..48515812-chr7:49402658..49405453,2	K562	blood:
4	chr7:48376280..48377237-chrX:150918854..150919433,2	MCF-7	breast:
5	chr7:48279225..48282090-chr7:48283159..48287155,3	K562	blood:
6	chr20:22370610..22371195-chr7:48238769..48239532,2	MCF-7	breast:
7	chr7:48350873..48351428-chr7:48826215..48827185,2	MCF-7	breast:
8	chr7:48375884..48377251-chr7:48914594..48915844,5	MCF-7	breast:
9	chr7:48339292..48339820-chr7:49892008..49892873,2	MCF-7	breast:
10	chr7:48376419..48377077-chr7:49891980..49892898,2	MCF-7	breast:
11	chr7:48279225..48282090-chr7:48283159..48287155,3	K562	blood:
12	chr7:48339343..48339865-chr7:49892019..49892834,2	K562	blood:
13	chr7:48464131..48464720-chr7:49830437..49831304,2	MCF-7	breast:
14	chr7:48338977..48339698-chr7:48914621..48915709,3	MCF-7	breast:
15	chr7:48464147..48465026-chr7:48914660..48915807,4	MCF-7	breast:
16	chr7:48464066..48464994-chr7:48914675..48915561,3	MCF-7	breast:

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

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

No data

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

Extended variants
information (count: 12406 )
Associated
traits (count: 126 )

Variant overlapped rSNPs/rCNVs (count:12406 , 50 per page) page: 1 2 3 4 5 6 7 ... 249

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs570878072	chr7:48238289-48238290	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs368034094	chr7:48238290-48238291	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs1997125	chr7:48238305-48238306	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs567497571	chr7:48238314-48238315	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs77947602	chr7:48238326-48238327	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs1997124	chr7:48238342-48238343	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs570141260	chr7:48238346-48238347	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs181924889	chr7:48238370-48238371	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs372356667	chr7:48238423-48238424	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs142174123	chr7:48238425-48238426	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs549435762	chr7:48238458-48238459	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs559110435	chr7:48238534-48238535	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs185713060	chr7:48238538-48238539	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs541068620	chr7:48238580-48238581	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs1917943	chr7:48238582-48238583	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs138717542	chr7:48238609-48238610	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs7788162	chr7:48238640-48238641	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs568377907	chr7:48238732-48238733	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs75211940	chr7:48238815-48238816	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs77431788	chr7:48238852-48238853	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs544663824	chr7:48238965-48238966	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs77143292	chr7:48238975-48238976	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs551630808	chr7:48239014-48239015	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs369646422	chr7:48239021-48239022	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs10278351	chr7:48239064-48239065	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs567534640	chr7:48239065-48239066	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs10224298	chr7:48239087-48239088	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs554056685	chr7:48239115-48239116	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs550070605	chr7:48239119-48239120	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs143434813	chr7:48239122-48239123	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs538843667	chr7:48239309-48239310	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs191601473	chr7:48239386-48239387	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs183856038	chr7:48239406-48239407	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs535005863	chr7:48239418-48239419	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs10281692	chr7:48239443-48239444	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs566686765	chr7:48239450-48239451	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs13247001	chr7:48239466-48239467	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs543727720	chr7:48239467-48239468	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs557244337	chr7:48239468-48239469	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs576978162	chr7:48239539-48239540	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs546035156	chr7:48239586-48239587	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs534037921	chr7:48239596-48239597	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs564630851	chr7:48239597-48239598	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs10237564	chr7:48239621-48239622	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs147985310	chr7:48239764-48239765	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs373408043	chr7:48239835-48239836	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs560693003	chr7:48239857-48239858	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs576433520	chr7:48239864-48239865	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs187954584	chr7:48239875-48239876	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs372930704	chr7:48239902-48239903	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:126)

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
Non-syndromic sensorineural hearing loss	22037309	CNVD
Autism	22495309	CNVD
Schizophrenia	23813976	CNVD

Chromatin state (count:955 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:48223200-48240400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
2	chr7:48230600-48246200	Strong transcription	Primary neutrophils fromperipheralblood	blood
3	chr7:48240200-48240400	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
4	chr7:48240200-48240800	Enhancers	Fetal Intestine Large	intestine
5	chr7:48240200-48240800	Enhancers	Fetal Intestine Small	intestine
6	chr7:48240200-48244200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr7:48240400-48241000	Active TSS	iPS-15b Cell Line	embryonic stem cell
8	chr7:48240400-48241200	Enhancers	iPS-18 Cell Line	embryonic stem cell
9	chr7:48240400-48241200	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
10	chr7:48240400-48241400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr7:48240400-48241400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
12	chr7:48240400-48241800	Enhancers	Stomach Mucosa	stomach
13	chr7:48240600-48241200	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
14	chr7:48240800-48241000	Active TSS	Fetal Intestine Small	intestine
15	chr7:48240800-48241200	Enhancers	Cortex derived primary cultured neurospheres	brain
16	chr7:48240800-48241200	Flanking Active TSS	Fetal Intestine Large	intestine
17	chr7:48240800-48241200	Active TSS	Rectal Mucosa Donor 29	rectum
18	chr7:48240800-48241200	Active TSS	Rectal Smooth Muscle	rectum
19	chr7:48240800-48241400	Active TSS	Duodenum Mucosa	Duodenum
20	chr7:48240800-48241600	Enhancers	K562	blood
21	chr7:48240800-48241800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr7:48241000-48241200	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
23	chr7:48241000-48241200	Flanking Active TSS	Fetal Intestine Small	intestine
24	chr7:48241200-48241600	Enhancers	Fetal Intestine Large	intestine
25	chr7:48241400-48243200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
26	chr7:48244200-48244600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr7:48246200-48247200	Weak transcription	Primary neutrophils fromperipheralblood	blood
28	chr7:48246400-48247400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
29	chr7:48247200-48248600	Enhancers	Primary neutrophils fromperipheralblood	blood
30	chr7:48248600-48250600	Weak transcription	Primary neutrophils fromperipheralblood	blood
31	chr7:48248600-48251200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
32	chr7:48250600-48251000	Enhancers	Primary neutrophils fromperipheralblood	blood
33	chr7:48251000-48252000	Genic enhancers	Primary neutrophils fromperipheralblood	blood
34	chr7:48251200-48252000	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
35	chr7:48252000-48253000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
36	chr7:48252000-48253400	Weak transcription	Primary neutrophils fromperipheralblood	blood
37	chr7:48253000-48253400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
38	chr7:48253000-48253400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
39	chr7:48253400-48278200	Strong transcription	Primary neutrophils fromperipheralblood	blood
40	chr7:48256800-48257200	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr7:48257200-48257600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr7:48274000-48274200	Bivalent Enhancer	Aorta	Aorta
43	chr7:48275400-48278000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
44	chr7:48277600-48290400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
45	chr7:48278200-48278600	Weak transcription	Primary neutrophils fromperipheralblood	blood
46	chr7:48278600-48279000	Strong transcription	Primary neutrophils fromperipheralblood	blood
47	chr7:48278800-48279200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
48	chr7:48279000-48279800	Genic enhancers	Primary neutrophils fromperipheralblood	blood
49	chr7:48279200-48279400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
50	chr7:48279400-48280400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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