Variant report

Variant	nsv970868
Chromosome Location	chr7:66035219-66056610
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:199)
CpG islands
(count:305)
Chromatin interactive
region (count:26)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:199 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BRCA1	chr7:66055470-66055522	GM12878	blood:	n/a	n/a
2	CBX3	chr7:66056063-66058024	K562	blood:	n/a	n/a
3	CEBPB	chr7:66052123-66052465	IMR90	lung:	n/a	chr7:66052296-66052307
4	CEBPB	chr7:66052151-66052368	A549	lung:	n/a	chr7:66052296-66052307
5	CEBPB	chr7:66052165-66052412	K562	blood:	n/a	chr7:66052296-66052307
6	CEBPB	chr7:66052163-66052365	Hela-S3	cervix:	n/a	chr7:66052296-66052307
7	CEBPB	chr7:66052139-66052428	HepG2	liver:	n/a	chr7:66052296-66052307
8	CHD1	chr7:66055223-66057756	IMR90	lung:	n/a	chr7:66057150-66057160
9	CHD2	chr7:66056201-66056325	K562	blood:	n/a	n/a
10	CTCF	chr7:66040380-66040530	HAc	cerebellar:	n/a	n/a
11	CTCF	chr7:66040380-66040530	HBMEC	blood vessel:	n/a	n/a
12	CTCF	chr7:66056002-66056078	Lung_OC	lung:	n/a	n/a
13	CTCF	chr7:66056540-66056690	SK-N-SH_RA	brain:	n/a	n/a
14	CTCF	chr7:66055910-66055965	LNCaP	prostate:	n/a	n/a
15	CUX1	chr7:66050686-66050789	K562	blood:	n/a	n/a
16	CUX1	chr7:66050212-66050480	K562	blood:	n/a	n/a
17	E2F6	chr7:66056129-66056346	K562	blood:	n/a	n/a
18	E2F6	chr7:66056142-66056318	K562	blood:	n/a	n/a
19	E2F6	chr7:66056485-66056806	K562	blood:	n/a	n/a
20	EBF1	chr7:66056366-66056582	GM12878	blood:	n/a	n/a
21	ELF1	chr7:66056542-66057553	GM12878	blood:	n/a	chr7:66056768-66056780 chr7:66057353-66057365
22	EP300	chr7:66056252-66056332	K562	blood:	n/a	n/a
23	EP300	chr7:66050747-66051017	K562	blood:	n/a	n/a
24	EP300	chr7:66050143-66050155	GM12878	blood:	n/a	n/a
25	FOS	chr7:66055696-66055957	MCF10A-Er-Src	breast:	n/a	n/a
26	FOS	chr7:66053328-66053551	MCF10A-Er-Src	breast:	n/a	n/a
27	FOS	chr7:66053342-66053551	MCF10A-Er-Src	breast:	n/a	n/a
28	FOS	chr7:66055696-66055961	MCF10A-Er-Src	breast:	n/a	n/a
29	FOSL2	chr7:66055810-66056068	HepG2	liver:	n/a	n/a
30	FOXA1	chr7:66040530-66040884	HepG2	liver:	n/a	n/a
31	FOXP2	chr7:66049558-66049904	PFSK-1	brain:	n/a	n/a
32	GABPA	chr7:66056584-66057701	K562	blood:	n/a	chr7:66057057-66057066
33	GATA2	chr7:66045011-66045359	K562	blood:	n/a	chr7:66045157-66045166
34	HA-E2F1	chr7:66056223-66057683	MCF-7	breast:	n/a	chr7:66057150-66057159
35	HCFC1	chr7:66056563-66057820	Hela-S3	cervix:	n/a	n/a
36	HDAC2	chr7:66055349-66055596	K562	blood:	n/a	n/a
37	HEY1	chr7:66055450-66055967	K562	blood:	n/a	n/a
38	HEY1	chr7:66056390-66056662	K562	blood:	n/a	n/a
39	HEY1	chr7:66056264-66056751	K562	blood:	n/a	n/a
40	HMGN3	chr7:66056602-66057537	K562	blood:	n/a	n/a
41	JUN	chr7:66056103-66057943	K562	blood:	n/a	chr7:66057182-66057191
42	MAFK	chr7:66046535-66046735	HepG2	liver:	n/a	chr7:66046579-66046594
43	MAFK	chr7:66046522-66046693	HepG2	liver:	n/a	chr7:66046579-66046594
44	MAX	chr7:66056180-66056278	Hela-S3	cervix:	n/a	n/a
45	MAX	chr7:66056046-66057789	K562	blood:	n/a	chr7:66056734-66056743
46	MAX	chr7:66056125-66056348	K562	blood:	n/a	n/a
47	MAX	chr7:66042781-66042791	GM12878	blood:	n/a	n/a
48	MAX	chr7:66055869-66055906	Hela-S3	cervix:	n/a	n/a
49	MAX	chr7:66048709-66048943	NB4	blood:	n/a	n/a
50	MAX	chr7:66056186-66056386	K562	blood:	n/a	n/a

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:66053803-66053853	HIPEpiC	eye:	n/a
2	chr7:66055597-66055647	HEK293	kidney:	embryo
3	chr7:66055597-66055647	ECC-1	luminal epithelium:	n/a
4	chr7:66044508-66044558	HIPEpiC	eye:	n/a
5	chr7:66053803-66053853	Jurkat	blood:	n/a
6	chr7:66044687-66044737	HIPEpiC	eye:	n/a
7	chr7:66044687-66044737	NHDF-neo	bronchial:	n/a
8	chr7:66055597-66055647	MCF10A-Er-Src	breast:	n/a
9	chr7:66044687-66044737	ovcar-3	ovarian:	n/a
10	chr7:66044687-66044737	HL-60	blood:	n/a
11	chr7:66043623-66043673	PANC-1	pancreas:	n/a
12	chr7:66044508-66044558	AG04450	lung:	fetal
13	chr7:66044508-66044558	SK-N-MC	brain:	n/a
14	chr7:66053803-66053853	HepG2	liver:	n/a
15	chr7:66044508-66044558	HRPEpiC	eye:	n/a
16	chr7:66043623-66043673	AG10803	skin:	n/a
17	chr7:66053803-66053853	AG09319	gingival:	n/a
18	chr7:66044687-66044737	Jurkat	blood:	n/a
19	chr7:66043623-66043673	HMEC	breast:	n/a
20	chr7:66053803-66053853	ECC-1	luminal epithelium:	n/a
21	chr7:66043623-66043673	AG04450	lung:	fetal
22	chr7:66053803-66053853	HL-60	blood:	n/a
23	chr7:66044687-66044737	HCT-116	colon:	n/a
24	chr7:66044687-66044737	HRE	kidney:	n/a
25	chr7:66044687-66044737	HPAEpiC	pulmonary alveolar:	n/a
26	chr7:66044508-66044558	HUVEC	blood vessel:	n/a
27	chr7:66055597-66055647	AG09309	skin:	n/a
28	chr7:66055597-66055647	GM19239	blood:	n/a
29	chr7:66053803-66053853	HCF	heart:	n/a
30	chr7:66043623-66043673	NHDF-neo	bronchial:	n/a
31	chr7:66044508-66044558	HPAEpiC	pulmonary alveolar:	n/a
32	chr7:66053803-66053853	HNPCEpiC	eye:	n/a
33	chr7:66044508-66044558	A549	lung:	n/a
34	chr7:66053803-66053853	SK-N-SH	brain:	n/a
35	chr7:66055597-66055647	H1-hESC	embryonic stem cell:	embryo
36	chr7:66055597-66055647	AG04450	lung:	fetal
37	chr7:66043623-66043673	ECC-1	luminal epithelium:	n/a
38	chr7:66044687-66044737	RPTEC	kidney:	n/a
39	chr7:66043623-66043673	HCM	heart:	n/a
40	chr7:66044508-66044558	AoSMC	blood vessel:	n/a
41	chr7:66043623-66043673	PFSK-1	brain:	n/a
42	chr7:66055597-66055647	HepG2	liver:	n/a
43	chr7:66055597-66055647	GM06990	blood:	n/a
44	chr7:66044508-66044558	Caco-2	colon:	n/a
45	chr7:66055597-66055647	NB4	blood:	n/a
46	chr7:66044687-66044737	ProgFib	skin:	n/a
47	chr7:66053803-66053853	HCM	heart:	n/a
48	chr7:66044508-66044558	Hepatocyte	liver:	n/a
49	chr7:66053803-66053853	HCT-116	colon:	n/a
50	chr7:66044508-66044558	HEK293	kidney:	embryo

(count:26 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:66034127..66036034-chr7:66040959..66043847,2	MCF-7	breast:
2	chr7:65930280..65931785-chr7:66046752..66048531,2	K562	blood:
3	chr7:66047534..66050313-chr7:66118210..66120231,2	K562	blood:
4	chr7:66055866..66057599-chr7:66093523..66095048,2	K562	blood:
5	chr7:66044695..66047717-chr7:66050273..66053007,3	K562	blood:
6	chr7:66046074..66047727-chr7:66051992..66054807,2	K562	blood:
7	chr7:66055924..66057616-chr7:66118024..66120875,2	K562	blood:
8	chr7:66051779..66054394-chr7:66057602..66059398,2	K562	blood:
9	chr7:66039081..66041475-chr7:66044716..66046904,2	K562	blood:
10	chr7:66049008..66051947-chr7:66055778..66057625,2	MCF-7	breast:
11	chr7:66044739..66046624-chr7:66048819..66050510,2	K562	blood:
12	chr7:66049357..66051342-chr7:66055893..66058877,2	K562	blood:
13	chr7:66054686..66058308-chr7:66092199..66095155,8	MCF-7	breast:
14	chr7:66044739..66046624-chr7:66048819..66050510,2	K562	blood:
15	chr7:66030313..66032213-chr7:66037914..66039587,2	MCF-7	breast:
16	chr7:66055516..66058509-chr7:66093670..66096346,2	MCF-7	breast:
17	chr7:66039081..66041475-chr7:66044716..66046904,2	K562	blood:
18	chr7:66055738..66058439-chr7:66119494..66121209,2	MCF-7	breast:
19	chr7:66047534..66050198-chr7:66118731..66121007,2	K562	blood:
20	chr7:66055703..66058887-chr7:66117840..66121190,6	MCF-7	breast:
21	chr7:66046074..66047727-chr7:66051992..66054807,2	K562	blood:
22	chr7:66052648..66055044-chr7:66119940..66122450,2	K562	blood:
23	chr7:66027953..66030074-chr7:66033611..66035977,2	K562	blood:
24	chr7:66044695..66047717-chr7:66050273..66053007,3	K562	blood:
25	chr7:66055717..66057230-chr7:66088670..66090655,2	K562	blood:
26	chr7:66050815..66053279-chr7:66056186..66059102,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SBDS-4	chr7:66049364-66049453	NONHSAT121209

No data

Variant related genes	Relation type
ENSG00000232559	TF binding region
ENSG00000232559	CpG island
ENSG00000243335	chromatin interactions
ENSG00000232559	chromatin interactions
ENSG00000226824	chromatin interactions

Extended variants
information (count: 950 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:950 , 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	rs182163427	chr7:66035231-66035232	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs370825512	chr7:66035243-66035244	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs578162473	chr7:66035263-66035264	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs574000674	chr7:66035274-66035275	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs535421154	chr7:66035366-66035367	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs572281645	chr7:66035382-66035383	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs546015863	chr7:66035383-66035384	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs559625815	chr7:66035486-66035487	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs553548678	chr7:66035487-66035488	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs573460703	chr7:66035560-66035561	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs545648176	chr7:66035566-66035567	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs528334011	chr7:66035606-66035607	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs565552024	chr7:66035612-66035613	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs575910445	chr7:66035619-66035620	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs543820525	chr7:66035681-66035682	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs560943018	chr7:66035844-66035845	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs964971	chr7:66035867-66035868	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
18	rs139862880	chr7:66035869-66035870	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs559841570	chr7:66035873-66035874	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs145497578	chr7:66035884-66035885	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs557545571	chr7:66035888-66035889	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs2013222	chr7:66035936-66035937	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
23	rs568769800	chr7:66035953-66035954	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs538142845	chr7:66035960-66035961	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs77406161	chr7:66035966-66035967	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs185166477	chr7:66036017-66036018	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs375280273	chr7:66036099-66036100	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs12530947	chr7:66036141-66036142	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
29	rs3857686	chr7:66036191-66036192	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
30	rs188761628	chr7:66036232-66036233	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs181236583	chr7:66036261-66036262	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs143196312	chr7:66036285-66036286	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs3087295	chr7:66036286-66036287	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs185335913	chr7:66036287-66036288	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs71526560	chr7:66036303-66036304	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs60113978	chr7:66036304-66036305	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs575801886	chr7:66036336-66036337	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs535743488	chr7:66036349-66036350	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs544878902	chr7:66036365-66036366	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs3898855	chr7:66036398-66036399	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
41	rs574351236	chr7:66036418-66036419	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs539862494	chr7:66036429-66036430	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs559780405	chr7:66036460-66036461	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs532085013	chr7:66036511-66036512	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs541509570	chr7:66036516-66036517	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs551904272	chr7:66036518-66036519	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs189800725	chr7:66036522-66036523	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs147687506	chr7:66036564-66036565	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs531449965	chr7:66036632-66036633	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs548452976	chr7:66036649-66036650	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:82)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17170743	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	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
Autism	22495311	CNVD
Follicular lymphoma	20505157	CNVD
Biliary cancer	19435499	CNVD
Williams-beuren syndrome	22470819	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Multiple myeloma	16461302	CNVD
Glioblastoma multiforme	21750150	CNVD
Cancer	21183584	CNVD
Hepatocellular carcinoma	16750200	CNVD
Non-small cell lung cancer	21829676	CNVD
Gastric cancer	24379144	CNVD
Glioblastoma multiforme	17002787	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Lissencephaly	21572526	CNVD
Breast cancer	17603634	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	16397240	CNVD
Acute myeloid leukemia	16864856	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Squamous cell cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	17387387	CNVD
Low-grade fibromyxoid sarcoma	0	CNVD
Oligodendroglial tumors	17285580	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21264507	CNVD
Shwachman-Diamond syndrome	22934832	CNVD
Glioblastoma	21080181	CNVD
Colorectal cancer	19359472	CNVD
Cutaneous malignant melanoma	17690212	CNVD
Leukemia	17361228	CNVD
Breast cancer	16461572	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Malignant melanoma	17690212	CNVD
Breast cancer	21990379	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	21399695	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Astrocytoma	22246337	CNVD
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
Acute monocytic leukemia	16498392	CNVD
Prostate cancer	16461572	CNVD
Salivary gland tumor	18059337	CNVD
Multiple myeloma	17550852	CNVD
Acute myeloid leukemia	21251322	CNVD
small cell lung cancer	20016488	CNVD
Bladder cancer	21909424	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Cancer	20164920	CNVD
Pancreatic cancer	17952125	CNVD
Prostate cancer	18632612	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:1162 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:66004400-66052600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr7:66004800-66037200	Weak transcription	Psoas Muscle	Psoas
3	chr7:66008600-66056000	Weak transcription	Pancreatic Islets	Pancreatic Islet
4	chr7:66011000-66037000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr7:66011600-66045000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr7:66019800-66036600	Weak transcription	HUVEC	blood vessel
7	chr7:66019800-66037400	Weak transcription	Rectal Smooth Muscle	rectum
8	chr7:66020000-66036600	Weak transcription	H9 Cell Line	embryonic stem cell
9	chr7:66020000-66037400	Weak transcription	Small Intestine	intestine
10	chr7:66021800-66056400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
11	chr7:66022000-66039000	Weak transcription	Aorta	Aorta
12	chr7:66023000-66036400	Weak transcription	Brain Substantia Nigra	brain
13	chr7:66023000-66036600	Weak transcription	Brain Anterior Caudate	brain
14	chr7:66023000-66036600	Weak transcription	Brain Cingulate Gyrus	brain
15	chr7:66023000-66037400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
16	chr7:66023000-66040800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
17	chr7:66023000-66041800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
18	chr7:66023200-66036800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
19	chr7:66023200-66043800	Weak transcription	Fetal Heart	heart
20	chr7:66023200-66044400	Weak transcription	Right Atrium	heart
21	chr7:66023200-66048400	Weak transcription	Colon Smooth Muscle	Colon
22	chr7:66023200-66049800	Weak transcription	Stomach Mucosa	stomach
23	chr7:66023200-66055400	Weak transcription	Fetal Brain Male	brain
24	chr7:66023600-66042200	Strong transcription	Monocytes-CD14+_RO01746	blood
25	chr7:66024000-66036600	Weak transcription	Skeletal Muscle Female	skeletal muscle
26	chr7:66024000-66036600	Weak transcription	Stomach Smooth Muscle	stomach
27	chr7:66024000-66037200	Weak transcription	Brain Hippocampus Middle	brain
28	chr7:66024000-66037200	Weak transcription	Colonic Mucosa	Colon
29	chr7:66024000-66037200	Weak transcription	Skeletal Muscle Male	skeletal muscle
30	chr7:66024000-66039000	Weak transcription	Right Ventricle	heart
31	chr7:66024000-66046400	Weak transcription	NHLF	lung
32	chr7:66024200-66036600	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
33	chr7:66024200-66037800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
34	chr7:66024200-66040400	Weak transcription	Placenta Amnion	Placenta Amnion
35	chr7:66024200-66051200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
36	chr7:66024200-66055400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
37	chr7:66024200-66055600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
38	chr7:66024400-66036000	Weak transcription	Duodenum Smooth Muscle	Duodenum
39	chr7:66024400-66036000	Weak transcription	Fetal Brain Female	brain
40	chr7:66024400-66036800	Weak transcription	Esophagus	oesophagus
41	chr7:66024400-66037200	Weak transcription	Brain Inferior Temporal Lobe	brain
42	chr7:66024400-66038800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
43	chr7:66024400-66051600	Weak transcription	Spleen	Spleen
44	chr7:66025200-66037200	Weak transcription	Cortex derived primary cultured neurospheres	brain
45	chr7:66027600-66042400	Strong transcription	Primary monocytes fromperipheralblood	blood
46	chr7:66028600-66038800	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
47	chr7:66028600-66042000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
48	chr7:66028800-66035600	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
49	chr7:66028800-66042000	Strong transcription	HUES6 Cell Line	embryonic stem cell
50	chr7:66028800-66042000	Strong transcription	Primary B cells from peripheral blood	blood

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