Variant report

Variant	nsv606894
Chromosome Location	chr7:48663637-48718598
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:340)
CpG islands
(count:122)
Chromatin interactive
region (count:2)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:340 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:48672196-48672569	K562	blood:	n/a	n/a
2	ARID3A	chr7:48672197-48672568	HepG2	liver:	n/a	n/a
3	ARID3A	chr7:48698567-48698751	K562	blood:	n/a	n/a
4	ATF1	chr7:48677125-48677363	K562	blood:	n/a	n/a
5	ATF1	chr7:48683091-48683338	K562	blood:	n/a	n/a
6	ATF1	chr7:48672195-48672569	K562	blood:	n/a	n/a
7	BACH1	chr7:48677071-48677315	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr7:48672197-48672570	K562	blood:	n/a	n/a
9	BACH1	chr7:48717937-48717986	H1-hESC	embryonic stem cell:	n/a	n/a
10	BATF	chr7:48677066-48677322	GM12878	blood:	n/a	chr7:48677196-48677206 chr7:48677199-48677210
11	BATF	chr7:48677111-48677301	GM12878	blood:	n/a	chr7:48677196-48677206 chr7:48677199-48677210
12	BCL11A	chr7:48672210-48672432	GM12878	blood:	n/a	n/a
13	BHLHE40	chr7:48673799-48674063	GM12878	blood:	n/a	n/a
14	BHLHE40	chr7:48683128-48683313	K562	blood:	n/a	n/a
15	BHLHE40	chr7:48672197-48672568	GM12878	blood:	n/a	n/a
16	BHLHE40	chr7:48701978-48702216	GM12878	blood:	n/a	n/a
17	BHLHE40	chr7:48672195-48672571	K562	blood:	n/a	n/a
18	BRCA1	chr7:48704048-48704080	GM12878	blood:	n/a	n/a
19	BRCA1	chr7:48672197-48672569	GM12878	blood:	n/a	n/a
20	BRCA1	chr7:48696844-48696882	Hela-S3	cervix:	n/a	n/a
21	BRCA1	chr7:48672196-48672570	Hela-S3	cervix:	n/a	n/a
22	CEBPB	chr7:48683142-48683424	K562	blood:	n/a	chr7:48683267-48683278 chr7:48683296-48683309 chr7:48683262-48683279 chr7:48683267-48683278 chr7:48683265-48683278 chr7:48683265-48683276
23	CEBPB	chr7:48672199-48672570	K562	blood:	n/a	n/a
24	CEBPB	chr7:48664704-48665008	IMR90	lung:	n/a	chr7:48664864-48664875
25	CEBPB	chr7:48704953-48705212	IMR90	lung:	n/a	chr7:48705073-48705086
26	CEBPB	chr7:48683116-48683308	K562	blood:	n/a	chr7:48683267-48683278 chr7:48683262-48683279 chr7:48683267-48683278 chr7:48683265-48683278 chr7:48683265-48683276
27	CEBPB	chr7:48666622-48666857	IMR90	lung:	n/a	n/a
28	CEBPB	chr7:48709012-48709194	A549	lung:	n/a	n/a
29	CEBPB	chr7:48664720-48665017	HepG2	liver:	n/a	chr7:48664864-48664875
30	CEBPB	chr7:48683113-48683457	HepG2	liver:	n/a	chr7:48683267-48683278 chr7:48683296-48683309 chr7:48683262-48683279 chr7:48683267-48683278 chr7:48683265-48683278 chr7:48683265-48683276
31	CEBPB	chr7:48666615-48666840	A549	lung:	n/a	n/a
32	CEBPB	chr7:48705007-48705155	H1-hESC	embryonic stem cell:	n/a	chr7:48705073-48705086
33	CEBPB	chr7:48664751-48665017	A549	lung:	n/a	chr7:48664864-48664875
34	CEBPB	chr7:48666572-48666889	HepG2	liver:	n/a	n/a
35	CEBPB	chr7:48703758-48703921	HepG2	liver:	n/a	n/a
36	CHD1	chr7:48672194-48672569	GM12878	blood:	n/a	n/a
37	CHD2	chr7:48672196-48672570	Hela-S3	cervix:	n/a	n/a
38	CHD2	chr7:48672196-48672569	K562	blood:	n/a	n/a
39	CHD2	chr7:48673973-48673981	GM12878	blood:	n/a	n/a
40	CTCF	chr7:48672288-48672458	A549	lung:	n/a	n/a
41	CTCF	chr7:48672280-48672430	AG09309	skin:	n/a	n/a
42	CTCF	chr7:48672320-48672470	HPAF	blood vessel:	n/a	n/a
43	CTCF	chr7:48672267-48672458	Fibrobl	skin:	n/a	n/a
44	CTCF	chr7:48672271-48672479	ProgFib	skin:	n/a	n/a
45	CTCF	chr7:48672360-48672510	HCT-116	colon:	n/a	n/a
46	CTCF	chr7:48697140-48697290	GM06990	blood:	n/a	n/a
47	CTCF	chr7:48676345-48676399	H1-hESC	embryonic stem cell:	n/a	n/a
48	CTCF	chr7:48672240-48672390	HepG2	liver:	n/a	n/a
49	CTCF	chr7:48672340-48672490	GM12873	blood:	n/a	n/a
50	CTCF	chr7:48672280-48672430	AoAF	blood vessel:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:48685182-48685232	Caco-2	colon:	n/a
2	chr7:48685182-48685232	PANC-1	pancreas:	n/a
3	chr7:48676611-48676661	HCM	heart:	n/a
4	chr7:48685182-48685232	A549	lung:	n/a
5	chr7:48676611-48676661	GM06990	blood:	n/a
6	chr7:48676611-48676661	HAEpiC	amniotic membrane:	n/a
7	chr7:48676611-48676661	GM12878	blood:	n/a
8	chr7:48685182-48685232	AG04449	skin:	fetal
9	chr7:48676611-48676661	SAEC	small airway:	n/a
10	chr7:48685182-48685232	Jurkat	blood:	n/a
11	chr7:48685182-48685232	HNPCEpiC	eye:	n/a
12	chr7:48685182-48685232	MCF10A-Er-Src	breast:	n/a
13	chr7:48676611-48676661	HCF	heart:	n/a
14	chr7:48676611-48676661	AoSMC	blood vessel:	n/a
15	chr7:48676611-48676661	K562	blood:	n/a
16	chr7:48685182-48685232	MCF-7	breast:	n/a
17	chr7:48676611-48676661	Hepatocyte	liver:	n/a
18	chr7:48676611-48676661	Caco-2	colon:	n/a
19	chr7:48685182-48685232	HPAEpiC	pulmonary alveolar:	n/a
20	chr7:48676611-48676661	NHBE	bronchial:	n/a
21	chr7:48685182-48685232	HRCEpiC	kidney:	n/a
22	chr7:48676611-48676661	IMR90	lung:	fetal
23	chr7:48676611-48676661	SK-N-MC	brain:	n/a
24	chr7:48685182-48685232	HRPEpiC	eye:	n/a
25	chr7:48676611-48676661	Jurkat	blood:	n/a
26	chr7:48685182-48685232	SK-N-SH_RA	brain:	n/a
27	chr7:48685182-48685232	CMK	blood:	n/a
28	chr7:48676611-48676661	ProgFib	skin:	n/a
29	chr7:48685182-48685232	Hela-S3	cervix:	n/a
30	chr7:48676611-48676661	HMEC	breast:	n/a
31	chr7:48685182-48685232	U87	brain:	n/a
32	chr7:48676611-48676661	RPTEC	kidney:	n/a
33	chr7:48676611-48676661	AG10803	skin:	n/a
34	chr7:48685182-48685232	NB4	blood:	n/a
35	chr7:48676611-48676661	AG04449	skin:	fetal
36	chr7:48685182-48685232	AG04450	lung:	fetal
37	chr7:48685182-48685232	HRE	kidney:	n/a
38	chr7:48685182-48685232	HMEC	breast:	n/a
39	chr7:48685182-48685232	ovcar-3	ovarian:	n/a
40	chr7:48676611-48676661	SK-N-SH_RA	brain:	n/a
41	chr7:48676611-48676661	HUVEC	blood vessel:	n/a
42	chr7:48685182-48685232	GM12891	blood:	n/a
43	chr7:48685182-48685232	NT2-D1	testis:	n/a
44	chr7:48676611-48676661	HCPEpiC	choroid plexus:	n/a
45	chr7:48685182-48685232	K562	blood:	n/a
46	chr7:48685182-48685232	HCT-116	colon:	n/a
47	chr7:48676611-48676661	SK-N-SH	brain:	n/a
48	chr7:48676611-48676661	SKMC	muscle:	n/a
49	chr7:48685182-48685232	SAEC	small airway:	n/a
50	chr7:48685182-48685232	PFSK-1	brain:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:48686744..48688752-chr7:48700122..48702748,2	K562	blood:
2	chr7:48686744..48688752-chr7:48700122..48702748,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SUN3-2	chr7:48702850-48702901	XLOC_006437
2	lnc-SUN3-2	chr7:48700171-48700491	XLOC_006437

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	ABCA13	hsa-miR-148b-3p	chr7:48682925-48682946

Variant related genes	Relation type
ENSG00000228173	TF binding region
ENSG00000228173	CpG island

Extended variants
information (count: 1267 )
Associated
traits (count: 121 )

Variant overlapped rSNPs/rCNVs (count:1267 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs3915483	chr7:48663637-48663638	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs536316473	chr7:48663649-48663650	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs373758839	chr7:48663652-48663653	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs113016382	chr7:48663655-48663656	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs67664236	chr7:48663656-48663657	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs5884055	chr7:48663685-48663686	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs3078326	chr7:48663690-48663691	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs3078355	chr7:48663696-48663697	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs575588823	chr7:48663745-48663746	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs544902465	chr7:48663819-48663820	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs564833652	chr7:48663823-48663824	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs572242988	chr7:48663831-48663832	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs367675020	chr7:48663938-48663939	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs10216285	chr7:48663941-48663942	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs186881584	chr7:48663944-48663945	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs116602038	chr7:48664020-48664021	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs369319391	chr7:48664031-48664032	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs191360256	chr7:48664035-48664036	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs182721057	chr7:48664065-48664066	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs186670414	chr7:48664079-48664080	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs140281153	chr7:48664103-48664104	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs201996807	chr7:48664124-48664125	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs71006571	chr7:48664128-48664129	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs68064783	chr7:48664129-48664130	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs56071738	chr7:48664140-48664141	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs200228509	chr7:48664141-48664142	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs80126837	chr7:48664143-48664144	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs74428770	chr7:48664157-48664158	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs28445700	chr7:48664159-48664160	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs535248346	chr7:48664163-48664164	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs10280980	chr7:48664196-48664197	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs10259747	chr7:48664201-48664202	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs555409110	chr7:48664203-48664204	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs573858530	chr7:48664220-48664221	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs137877274	chr7:48664254-48664255	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs575677130	chr7:48664294-48664295	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs538236610	chr7:48664373-48664374	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs558453605	chr7:48664445-48664446	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs572274889	chr7:48664464-48664465	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs544025100	chr7:48664469-48664470	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs573939531	chr7:48664481-48664482	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs541287592	chr7:48664502-48664503	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs75231568	chr7:48664545-48664546	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs574528496	chr7:48664599-48664600	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs374389664	chr7:48664618-48664619	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs575346494	chr7:48664624-48664625	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs543981365	chr7:48664656-48664657	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs201065877	chr7:48664699-48664700	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs563764130	chr7:48664757-48664758	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs532586606	chr7:48664767-48664768	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:121)

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
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:193 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:48635800-48672200	Weak transcription	Primary hematopoietic stem cells	blood
2	chr7:48650200-48672200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr7:48654800-48669400	Strong transcription	Primary neutrophils fromperipheralblood	blood
4	chr7:48661600-48672200	Weak transcription	Fetal Lung	lung
5	chr7:48662800-48664200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
6	chr7:48663400-48665000	Weak transcription	Thymus	Thymus
7	chr7:48665000-48668600	Enhancers	Thymus	Thymus
8	chr7:48665200-48667800	Enhancers	Fetal Thymus	thymus
9	chr7:48665800-48667000	Enhancers	Primary T cells from cord blood	blood
10	chr7:48667800-48668600	Weak transcription	Fetal Thymus	thymus
11	chr7:48668400-48668800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr7:48668400-48669600	Enhancers	Fetal Heart	heart
13	chr7:48668600-48669400	Enhancers	Fetal Thymus	thymus
14	chr7:48669200-48669400	Enhancers	Left Ventricle	heart
15	chr7:48669400-48672200	Weak transcription	Primary neutrophils fromperipheralblood	blood
16	chr7:48669400-48672200	Weak transcription	Left Ventricle	heart
17	chr7:48669600-48672200	Weak transcription	Fetal Heart	heart
18	chr7:48670000-48670200	Enhancers	Fetal Kidney	kidney
19	chr7:48671800-48672200	Weak transcription	Fetal Kidney	kidney
20	chr7:48672200-48672400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr7:48672200-48672400	ZNF genes & repeats	iPS-15b Cell Line	embryonic stem cell
22	chr7:48672200-48672400	ZNF genes & repeats	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
23	chr7:48672200-48672400	ZNF genes & repeats	Primary T helper memory cells from peripheral blood 2	blood
24	chr7:48672200-48672400	ZNF genes & repeats	Primary T helper naive cells from peripheral blood	blood
25	chr7:48672200-48672400	ZNF genes & repeats	Primary T helper memory cells from peripheral blood 1	blood
26	chr7:48672200-48672400	ZNF genes & repeats	Primary T cells effector/memory enriched fromperipheralblood	blood
27	chr7:48672200-48672400	ZNF genes & repeats	Primary T killer memory cells from peripheral blood	blood
28	chr7:48672200-48672400	ZNF genes & repeats	Muscle Satellite Cultured Cells	--
29	chr7:48672200-48672400	Flanking Bivalent TSS/Enh	Adipose Nuclei	Adipose
30	chr7:48672200-48672400	Enhancers	Fetal Kidney	kidney
31	chr7:48672200-48672400	ZNF genes & repeats	Fetal Lung	lung
32	chr7:48672200-48672400	Flanking Bivalent TSS/Enh	Right Ventricle	heart
33	chr7:48672200-48672400	Bivalent Enhancer	Sigmoid Colon	Sigmoid Colon
34	chr7:48672200-48672400	Bivalent Enhancer	Stomach Smooth Muscle	stomach
35	chr7:48672200-48672600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
36	chr7:48672200-48672600	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
37	chr7:48672200-48672600	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr7:48672200-48672600	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
39	chr7:48672200-48672600	ZNF genes & repeats	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
40	chr7:48672200-48672600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
41	chr7:48672200-48672600	ZNF genes & repeats	Primary neutrophils fromperipheralblood	blood
42	chr7:48672200-48672600	ZNF genes & repeats	Primary hematopoietic stem cells	blood
43	chr7:48672200-48672600	ZNF genes & repeats	Primary T helper naive cells fromperipheralblood	blood
44	chr7:48672200-48672600	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Female	--
45	chr7:48672200-48672600	Enhancers	Aorta	Aorta
46	chr7:48672200-48672600	Bivalent/Poised TSS	Brain Cingulate Gyrus	brain
47	chr7:48672200-48672600	ZNF genes & repeats	Brain Dorsolateral Prefrontal Cortex	brain
48	chr7:48672200-48672600	ZNF genes & repeats	Esophagus	oesophagus
49	chr7:48672200-48672600	ZNF genes & repeats	Fetal Heart	heart
50	chr7:48672200-48672600	Flanking Bivalent TSS/Enh	Gastric	stomach

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