Variant report

Variant	nsv882177
Chromosome Location	chr5:70800538-70856378
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:186)
CpG islands
(count:122)
Chromatin interactive
region (count:8)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:3)

(count:186 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr5:70829509-70829816	K562	blood:	n/a	n/a
2	BACH1	chr5:70834714-70834715	K562	blood:	n/a	n/a
3	BATF	chr5:70829035-70829290	GM12878	blood:	n/a	chr5:70829133-70829144
4	BHLHE40	chr5:70829324-70829553	K562	blood:	n/a	n/a
5	CEBPB	chr5:70831081-70831112	HepG2	liver:	n/a	chr5:70831084-70831095
6	CREB1	chr5:70829476-70829744	A549	lung:	n/a	n/a
7	CREB1	chr5:70829388-70829883	GM12878	blood:	n/a	n/a
8	CREB1	chr5:70829401-70829905	GM12878	blood:	n/a	n/a
9	CTCF	chr5:70807378-70807465	GM10248	blood:	n/a	n/a
10	CTCF	chr5:70831460-70831610	HEK293	kidney:	n/a	n/a
11	CTCF	chr5:70846107-70846140	Kidney_OC	kidney:	n/a	n/a
12	CTCF	chr5:70831440-70831590	A549	lung:	n/a	n/a
13	CTCF	chr5:70845800-70845950	GM12869	blood:	n/a	n/a
14	CUX1	chr5:70834825-70834849	GM12878	blood:	n/a	n/a
15	E2F4	chr5:70841810-70842010	MCF10A-Er-Src	breast:	n/a	n/a
16	E2F4	chr5:70812889-70813089	MCF10A-Er-Src	breast:	n/a	n/a
17	E2F4	chr5:70825494-70825694	MCF10A-Er-Src	breast:	n/a	n/a
18	E2F4	chr5:70840114-70840314	MCF10A-Er-Src	breast:	n/a	n/a
19	E2F4	chr5:70824219-70824419	MCF10A-Er-Src	breast:	n/a	n/a
20	E2F4	chr5:70806466-70806612	MCF10A-Er-Src	breast:	n/a	n/a
21	EBF1	chr5:70852375-70852555	GM12878	blood:	n/a	n/a
22	EBF1	chr5:70840877-70840886	GM12878	blood:	n/a	n/a
23	ELK1	chr5:70810942-70810947	GM12878	blood:	n/a	n/a
24	EP300	chr5:70829010-70829309	K562	blood:	n/a	n/a
25	EP300	chr5:70825570-70825701	GM12878	blood:	n/a	n/a
26	EP300	chr5:70849060-70849098	GM12878	blood:	n/a	n/a
27	FOS	chr5:70824128-70824437	MCF10A-Er-Src	breast:	n/a	chr5:70824257-70824267 chr5:70824257-70824267 chr5:70824257-70824267
28	FOS	chr5:70828984-70829320	MCF10A-Er-Src	breast:	n/a	n/a
29	FOS	chr5:70828999-70829300	MCF10A-Er-Src	breast:	n/a	n/a
30	FOS	chr5:70824138-70824367	MCF10A-Er-Src	breast:	n/a	chr5:70824257-70824267 chr5:70824257-70824267 chr5:70824257-70824267
31	FOS	chr5:70824123-70824454	MCF10A-Er-Src	breast:	n/a	chr5:70824257-70824267 chr5:70824257-70824267 chr5:70824257-70824267
32	FOS	chr5:70828984-70829323	MCF10A-Er-Src	breast:	n/a	n/a
33	FOS	chr5:70828966-70829323	MCF10A-Er-Src	breast:	n/a	n/a
34	GATA3	chr5:70823439-70823618	SH-SY5Y	brain:	n/a	n/a
35	GATA3	chr5:70804551-70804980	T-47D	breast:	n/a	chr5:70804913-70804924
36	GATA3	chr5:70804649-70804939	T-47D	breast:	n/a	chr5:70804913-70804924
37	GATA3	chr5:70804586-70804968	MCF-7	breast:	n/a	chr5:70804913-70804924
38	GATA3	chr5:70804714-70804914	SH-SY5Y	brain:	n/a	n/a
39	GATA3	chr5:70808009-70808265	SH-SY5Y	brain:	n/a	n/a
40	HCFC1	chr5:70824059-70824110	K562	blood:	n/a	n/a
41	IRF1	chr5:70829087-70829195	K562	blood:	n/a	n/a
42	IRF1	chr5:70828939-70829338	K562	blood:	n/a	n/a
43	IRF1	chr5:70813065-70813095	K562	blood:	n/a	n/a
44	IRF3	chr5:70811790-70811862	GM12878	blood:	n/a	n/a
45	JUN	chr5:70837029-70837119	H1-hESC	embryonic stem cell:	n/a	n/a
46	JUN	chr5:70811182-70811277	K562	blood:	n/a	n/a
47	JUND	chr5:70829058-70829330	K562	blood:	n/a	n/a
48	MAFF	chr5:70828962-70829304	K562	blood:	n/a	n/a
49	MAFF	chr5:70836857-70837047	K562	blood:	n/a	n/a
50	MAFF	chr5:70819987-70820037	K562	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:70848105-70848155	SK-N-SH_RA	brain:	n/a
2	chr5:70848105-70848155	SK-N-SH	brain:	n/a
3	chr5:70848529-70848579	GM12891	blood:	n/a
4	chr5:70848105-70848155	AoSMC	blood vessel:	n/a
5	chr5:70848105-70848155	NHBE	bronchial:	n/a
6	chr5:70848529-70848579	NHDF-neo	bronchial:	n/a
7	chr5:70848105-70848155	MCF-7	breast:	n/a
8	chr5:70848529-70848579	AG10803	skin:	n/a
9	chr5:70848105-70848155	Jurkat	blood:	n/a
10	chr5:70848529-70848579	HUVEC	blood vessel:	n/a
11	chr5:70848529-70848579	SK-N-SH_RA	brain:	n/a
12	chr5:70848105-70848155	SKMC	muscle:	n/a
13	chr5:70848529-70848579	A549	lung:	n/a
14	chr5:70848105-70848155	HPAEpiC	pulmonary alveolar:	n/a
15	chr5:70848105-70848155	HCF	heart:	n/a
16	chr5:70848529-70848579	HRE	kidney:	n/a
17	chr5:70848529-70848579	NB4	blood:	n/a
18	chr5:70848105-70848155	ECC-1	luminal epithelium:	n/a
19	chr5:70848529-70848579	HNPCEpiC	eye:	n/a
20	chr5:70848105-70848155	AG04449	skin:	fetal
21	chr5:70848105-70848155	U87	brain:	n/a
22	chr5:70848529-70848579	HAEpiC	amniotic membrane:	n/a
23	chr5:70848105-70848155	HCT-116	colon:	n/a
24	chr5:70848529-70848579	HEK293	kidney:	embryo
25	chr5:70848105-70848155	GM12878	blood:	n/a
26	chr5:70848529-70848579	AG09309	skin:	n/a
27	chr5:70848105-70848155	HCM	heart:	n/a
28	chr5:70848529-70848579	GM19239	blood:	n/a
29	chr5:70848529-70848579	HMEC	breast:	n/a
30	chr5:70848529-70848579	GM12878	blood:	n/a
31	chr5:70848105-70848155	ovcar-3	ovarian:	n/a
32	chr5:70848105-70848155	SAEC	small airway:	n/a
33	chr5:70848529-70848579	NHBE	bronchial:	n/a
34	chr5:70848105-70848155	HRE	kidney:	n/a
35	chr5:70848529-70848579	HCT-116	colon:	n/a
36	chr5:70848529-70848579	MCF10A-Er-Src	breast:	n/a
37	chr5:70848529-70848579	SK-N-MC	brain:	n/a
38	chr5:70848529-70848579	T-47D	breast:	n/a
39	chr5:70848105-70848155	CMK	blood:	n/a
40	chr5:70848105-70848155	MCF10A-Er-Src	breast:	n/a
41	chr5:70848105-70848155	AG04450	lung:	fetal
42	chr5:70848105-70848155	IMR90	lung:	fetal
43	chr5:70848105-70848155	HRPEpiC	eye:	n/a
44	chr5:70848105-70848155	ProgFib	skin:	n/a
45	chr5:70848105-70848155	BE2_C	brain:	n/a
46	chr5:70848529-70848579	LNCaP	prostate:	n/a
47	chr5:70848105-70848155	LNCaP	prostate:	n/a
48	chr5:70848529-70848579	HepG2	liver:	n/a
49	chr5:70848105-70848155	HAEpiC	amniotic membrane:	n/a
50	chr5:70848105-70848155	NT2-D1	testis:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr5:70848453..70850965-chr5:70856159..70858159,2	K562	blood:
2	chr5:70799887..70801582-chr5:70804594..70806211,2	K562	blood:
3	chr5:70848453..70850965-chr5:70856159..70858159,2	K562	blood:
4	chr5:70779922..70782030-chr5:70836622..70838928,2	K562	blood:
5	chr5:70829837..70831785-chr5:70927943..70929990,2	MCF-7	breast:
6	chr5:70799887..70801582-chr5:70804594..70806211,2	K562	blood:
7	chr5:70751568..70754307-chr5:70852249..70853965,2	K562	blood:
8	chr5:70794892..70797497-chr5:70800598..70802623,2	K562	blood:

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location
1	BDP1	hsa-miR-186-5p	chr5:70807134-70807155
2	BDP1	hsa-miR-186-5p	chr5:70841150-70841171
3	BDP1	hsa-miR-186-5p	chr5:70841139-70841160

Variant related genes	Relation type
BDP1	TF binding region
HMGN1P12	TF binding region
BDP1	CpG island
HMGN1P12	CpG island

Extended variants
information (count: 2245 )
Associated
traits (count: 104 )

Variant overlapped rSNPs/rCNVs (count:2245 , 50 per page) page: 1 2 3 4 5 6 7 ... 45

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs3761967	chr5:70800538-70800539	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs200613798	chr5:70800544-70800545	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs201477835	chr5:70800559-70800560	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs371121326	chr5:70800567-70800568	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs572240859	chr5:70800682-70800683	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs531374918	chr5:70800685-70800686	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs115991484	chr5:70800695-70800696	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs564992559	chr5:70800710-70800711	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs569042296	chr5:70800713-70800714	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs141801419	chr5:70800730-70800731	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs548402298	chr5:70800759-70800760	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs532363300	chr5:70800767-70800768	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs547760049	chr5:70800787-70800788	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs565669250	chr5:70800788-70800789	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs191936295	chr5:70800825-70800826	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs562597256	chr5:70800849-70800850	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs140699095	chr5:70800863-70800864	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs74749825	chr5:70800972-70800973	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs374001	chr5:70801018-70801019	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs536473881	chr5:70801096-70801097	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs184239160	chr5:70801114-70801115	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs146593455	chr5:70801139-70801140	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs552895170	chr5:70801140-70801141	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs186012910	chr5:70801238-70801239	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs537791308	chr5:70801257-70801258	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs6452900	chr5:70801354-70801355	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs117981212	chr5:70801369-70801370	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs535186658	chr5:70801372-70801373	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs553862107	chr5:70801411-70801412	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs190778778	chr5:70801482-70801483	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs546022380	chr5:70801487-70801488	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs392791	chr5:70801539-70801540	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
33	rs367803588	chr5:70801569-70801570	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs544172787	chr5:70801586-70801587	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs562526216	chr5:70801588-70801589	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs533648560	chr5:70801667-70801668	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs530134510	chr5:70801679-70801680	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs541954706	chr5:70801754-70801755	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs373589833	chr5:70801840-70801841	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs62374365	chr5:70801862-70801863	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs576473560	chr5:70801880-70801881	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs113482723	chr5:70801887-70801888	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs560675907	chr5:70801913-70801914	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs527838765	chr5:70801998-70801999	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs552805225	chr5:70802085-70802086	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs183093610	chr5:70802111-70802112	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs371688723	chr5:70802182-70802183	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs550531353	chr5:70802193-70802194	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs555186054	chr5:70802214-70802215	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs2432060	chr5:70802241-70802242	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance

Variant related diseases (count:104)

Disease	PMID	Source
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Metanephric adenoma	20802469	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Multiple myeloma	17550852	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Cancer	16751803	CNVD
Intellectual disability	22102821	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Breast cancer	22032731	CNVD
Prostate cancer	21965145	CNVD
Spinal muscular atrophy	21762474	CNVD
Esophageal cancer	20955586	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Ovarian cancer	20844748	CNVD
Breast cancer	17393978	CNVD
Cancer	21359685	CNVD
Non-small cell lung cancer	21829676	CNVD
adenomatous polyposis	22470819	CNVD
Cancer	22429812	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Liposarcoma	21253554	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Breast cancer	21858162	CNVD
Hepatocellular carcinoma	16750200	CNVD
Leukemia	17361228	CNVD
Myelodysplastic syndrome	18508791	CNVD
5q-syndrome	17576883	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	16740712	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Urothelial carcinoma	21177765	CNVD
Acute myeloid leukemia	21251322	CNVD
Oral cancer	21386901	CNVD
Bladder cancer	21909424	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Breast cancer	17133270	CNVD
Breast cancer	19602461	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Retinoblastoma	22278416	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	CNVD
abnormal development	18461090	CNVD
Merkel cell carcinoma	19020549	CNVD
Squamous cell cancer	20885788	CNVD
Neurodevelopmental disorder	22521361	CNVD
Prostate cancer	18632612	CNVD
Ovarian cancer	21720365	CNVD
Breast cancer	21045282	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Myelodysplastic syndrome	18663149	CNVD
Spinal muscular atrophy	15981080	CNVD
Spinal muscular atrophy	18839960	CNVD
Spinal muscular atrophy	19716110	CNVD
Sezary syndrome	18413736	CNVD
Breast cancer	21990379	CNVD
Hirschsprung''s Disease	21712996	CNVD
Apoptosis	19488400	CNVD
Breast cancer	22048815	CNVD
Myelofibrosis	22110671	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Acute monocytic leukemia	16498392	CNVD
Colorectal cancer	20459617	CNVD
Gastric adenocarcinoma	19115996	CNVD
Spinal muscular atrophy	17160897	CNVD
Spinal muscular atrophy	17668391	CNVD
Spinal muscular atrophy	17668395	CNVD
Glioblastoma multiforme	22286061	CNVD
craniofacial dysmorphism	21918468	CNVD
Multiple myeloma	16616336	CNVD
Prostate cancer	16461572	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Acute myeloid leukemia	20729466	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1699 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:70754200-70815800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr5:70754400-70807200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
3	chr5:70754400-70809800	Strong transcription	Fetal Intestine Large	intestine
4	chr5:70754400-70824200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr5:70754600-70820400	Strong transcription	Primary T helper cells fromperipheralblood	blood
6	chr5:70754600-70820400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
7	chr5:70759800-70833400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
8	chr5:70765400-70820400	Strong transcription	Primary monocytes fromperipheralblood	blood
9	chr5:70765400-70820400	Strong transcription	Primary B cells from peripheral blood	blood
10	chr5:70766000-70820400	Strong transcription	Monocytes-CD14+_RO01746	blood
11	chr5:70766200-70807000	Strong transcription	Fetal Muscle Trunk	muscle
12	chr5:70771400-70820400	Strong transcription	HUES64 Cell Line	embryonic stem cell
13	chr5:70774400-70820400	Strong transcription	Fetal Thymus	thymus
14	chr5:70775600-70821000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
15	chr5:70776000-70806200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
16	chr5:70776400-70819200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr5:70776400-70820400	Strong transcription	HUES48 Cell Line	embryonic stem cell
18	chr5:70776400-70820400	Strong transcription	Primary T cells fromperipheralblood	blood
19	chr5:70776400-70820400	Strong transcription	Duodenum Mucosa	Duodenum
20	chr5:70776600-70820400	Strong transcription	HUES6 Cell Line	embryonic stem cell
21	chr5:70776800-70820400	Strong transcription	iPS-20b Cell Line	embryonic stem cell
22	chr5:70776800-70820400	Strong transcription	Dnd41	blood
23	chr5:70777600-70837600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
24	chr5:70777800-70816400	Strong transcription	iPS-18 Cell Line	embryonic stem cell
25	chr5:70778200-70807000	Strong transcription	Rectal Mucosa Donor 29	rectum
26	chr5:70778400-70810000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
27	chr5:70778400-70816400	Strong transcription	Rectal Mucosa Donor 31	rectum
28	chr5:70778400-70869600	Weak transcription	Stomach Mucosa	stomach
29	chr5:70779000-70807000	Strong transcription	Duodenum Smooth Muscle	Duodenum
30	chr5:70779000-70820400	Strong transcription	Primary T helper cells PMA-I stimulated	--
31	chr5:70779000-70820600	Strong transcription	Liver	Liver
32	chr5:70779200-70812400	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
33	chr5:70779200-70820600	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
34	chr5:70779400-70820400	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
35	chr5:70779600-70802400	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
36	chr5:70779800-70809000	Strong transcription	Primary T cells from cord blood	blood
37	chr5:70780000-70820400	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
38	chr5:70780200-70806200	Weak transcription	Psoas Muscle	Psoas
39	chr5:70780200-70820400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
40	chr5:70783000-70811200	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
41	chr5:70785200-70802400	Strong transcription	Stomach Smooth Muscle	stomach
42	chr5:70786200-70800600	Strong transcription	A549	lung
43	chr5:70786200-70805600	Weak transcription	Fetal Brain Male	brain
44	chr5:70788000-70819000	Weak transcription	Pancreatic Islets	Pancreatic Islet
45	chr5:70789600-70825400	Weak transcription	Fetal Heart	heart
46	chr5:70789800-70801600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
47	chr5:70790200-70804400	Strong transcription	Fetal Intestine Small	intestine
48	chr5:70790200-70804600	Strong transcription	Fetal Stomach	stomach
49	chr5:70790200-70816800	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
50	chr5:70790400-70820400	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung

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