Variant report

Variant	nsv933016
Chromosome Location	chr5:147395849-147453701
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	CBX3	chr5:147434864-147435069	K562	blood:	n/a	n/a
2	CCNT2	chr5:147414502-147414684	K562	blood:	n/a	n/a
3	CEBPB	chr5:147412698-147412976	H1-hESC	embryonic stem cell:	n/a	chr5:147412825-147412838
4	CEBPB	chr5:147418846-147418986	Hela-S3	cervix:	n/a	chr5:147418926-147418937
5	CEBPB	chr5:147418802-147419070	HepG2	liver:	n/a	chr5:147418926-147418937
6	CEBPB	chr5:147418836-147419047	A549	lung:	n/a	chr5:147418926-147418937
7	CEBPB	chr5:147443606-147443759	Hela-S3	cervix:	n/a	n/a
8	CEBPB	chr5:147418757-147419079	IMR90	lung:	n/a	chr5:147418926-147418937
9	CEBPB	chr5:147422501-147422663	H1-hESC	embryonic stem cell:	n/a	chr5:147422647-147422658 chr5:147422648-147422659
10	CEBPB	chr5:147412654-147413105	Hela-S3	cervix:	n/a	chr5:147412825-147412838
11	CEBPB	chr5:147422543-147422729	HepG2	liver:	n/a	chr5:147422647-147422658 chr5:147422648-147422659
12	CEBPB	chr5:147399747-147400237	Hela-S3	cervix:	n/a	chr5:147400195-147400208
13	CEBPB	chr5:147418914-147418948	K562	blood:	n/a	chr5:147418926-147418937
14	CHD2	chr5:147399817-147400155	Hela-S3	cervix:	n/a	n/a
15	CHD2	chr5:147412774-147413110	Hela-S3	cervix:	n/a	n/a
16	CTCF	chr5:147430745-147430817	GM10266	blood:	n/a	n/a
17	CTCF	chr5:147453700-147453850	BE2_C	brain:	n/a	n/a
18	CTCF	chr5:147447760-147447910	Hela-S3	cervix:	n/a	n/a
19	E2F4	chr5:147443606-147443961	MCF10A-Er-Src	breast:	n/a	n/a
20	E2F4	chr5:147430569-147430720	MCF10A-Er-Src	breast:	n/a	n/a
21	E2F4	chr5:147412679-147413061	MCF10A-Er-Src	breast:	n/a	n/a
22	EP300	chr5:147399806-147400270	Hela-S3	cervix:	n/a	n/a
23	EP300	chr5:147412750-147413050	Hela-S3	cervix:	n/a	chr5:147412911-147412918
24	ESR1	chr5:147449920-147450370	T-47D	breast:	n/a	chr5:147450140-147450157
25	ESR1	chr5:147449960-147450380	T-47D	breast:	n/a	chr5:147450140-147450157
26	ESR1	chr5:147449855-147450362	T-47D	breast:	n/a	chr5:147450140-147450157
27	ESR1	chr5:147449990-147450322	T-47D	breast:	n/a	chr5:147450140-147450157
28	ESR1	chr5:147449970-147450341	T-47D	breast:	n/a	chr5:147450140-147450157
29	ESR1	chr5:147449966-147450390	T-47D	breast:	n/a	chr5:147450140-147450157
30	FOS	chr5:147443456-147443906	MCF10A-Er-Src	breast:	n/a	n/a
31	FOS	chr5:147412651-147413124	MCF10A-Er-Src	breast:	n/a	n/a
32	FOS	chr5:147430486-147430798	MCF10A-Er-Src	breast:	n/a	n/a
33	FOS	chr5:147451872-147452314	MCF10A-Er-Src	breast:	n/a	chr5:147452270-147452281
34	FOS	chr5:147443460-147443966	MCF10A-Er-Src	breast:	n/a	chr5:147443913-147443925
35	FOS	chr5:147443430-147443906	MCF10A-Er-Src	breast:	n/a	n/a
36	FOS	chr5:147440426-147440727	MCF10A-Er-Src	breast:	n/a	n/a
37	FOS	chr5:147451884-147452432	MCF10A-Er-Src	breast:	n/a	chr5:147452270-147452281
38	FOS	chr5:147430514-147430767	MCF10A-Er-Src	breast:	n/a	n/a
39	FOS	chr5:147443477-147443961	MCF10A-Er-Src	breast:	n/a	chr5:147443913-147443925
40	FOS	chr5:147452054-147452415	MCF10A-Er-Src	breast:	n/a	chr5:147452270-147452281
41	FOS	chr5:147451896-147452429	MCF10A-Er-Src	breast:	n/a	chr5:147452270-147452281
42	FOS	chr5:147430461-147430786	MCF10A-Er-Src	breast:	n/a	n/a
43	FOS	chr5:147412663-147413091	MCF10A-Er-Src	breast:	n/a	n/a
44	FOS	chr5:147440393-147440761	MCF10A-Er-Src	breast:	n/a	n/a
45	FOS	chr5:147412754-147413091	MCF10A-Er-Src	breast:	n/a	n/a
46	FOS	chr5:147412723-147413097	MCF10A-Er-Src	breast:	n/a	n/a
47	FOS	chr5:147440390-147440809	MCF10A-Er-Src	breast:	n/a	chr5:147440777-147440789
48	FOS	chr5:147432442-147432753	HUVEC	blood vessel:	n/a	chr5:147432583-147432594
49	FOS	chr5:147440408-147440777	MCF10A-Er-Src	breast:	n/a	n/a
50	FOXA1	chr5:147450117-147450335	T-47D	breast:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:147443536-147443586	HEEpiC	esophagus:	n/a
2	chr5:147443347-147443397	HUVEC	blood vessel:	n/a
3	chr5:147443536-147443586	HEEpiC	esophagus:	n/a
4	chr5:147443347-147443397	HUVEC	blood vessel:	n/a
5	chr5:147443536-147443586	Caco-2	colon:	n/a
6	chr5:147443284-147443334	HUVEC	blood vessel:	n/a
7	chr5:147443536-147443586	HIPEpiC	eye:	n/a
8	chr5:147443536-147443586	HRCEpiC	kidney:	n/a
9	chr5:147443347-147443397	HCM	heart:	n/a
10	chr5:147443067-147443117	PFSK-1	brain:	n/a
11	chr5:147443347-147443397	AoSMC	blood vessel:	n/a
12	chr5:147443284-147443334	CMK	blood:	n/a
13	chr5:147443536-147443586	HL-60	blood:	n/a
14	chr5:147443067-147443117	PANC-1	pancreas:	n/a
15	chr5:147443284-147443334	MCF-7	breast:	n/a
16	chr5:147443284-147443334	HPAEpiC	pulmonary alveolar:	n/a
17	chr5:147443347-147443397	ovcar-3	ovarian:	n/a
18	chr5:147443284-147443334	NB4	blood:	n/a
19	chr5:147443536-147443586	Hepatocyte	liver:	n/a
20	chr5:147443067-147443117	ovcar-3	ovarian:	n/a
21	chr5:147443284-147443334	U87	brain:	n/a
22	chr5:147443067-147443117	NB4	blood:	n/a
23	chr5:147443252-147443302	HEK293	kidney:	embryo
24	chr5:147443284-147443334	SK-N-SH	brain:	n/a
25	chr5:147443347-147443397	GM12892	blood:	n/a
26	chr5:147443284-147443334	T-47D	breast:	n/a
27	chr5:147443536-147443586	HCPEpiC	choroid plexus:	n/a
28	chr5:147443284-147443334	Hela-S3	cervix:	n/a
29	chr5:147443347-147443397	U87	brain:	n/a
30	chr5:147443252-147443302	NB4	blood:	n/a
31	chr5:147443536-147443586	SK-N-SH_RA	brain:	n/a
32	chr5:147443252-147443302	AG09309	skin:	n/a
33	chr5:147443347-147443397	BE2_C	brain:	n/a
34	chr5:147443284-147443334	HepG2	liver:	n/a
35	chr5:147443252-147443302	GM12892	blood:	n/a
36	chr5:147443252-147443302	NHBE	bronchial:	n/a
37	chr5:147443347-147443397	HPAEpiC	pulmonary alveolar:	n/a
38	chr5:147443252-147443302	AG10803	skin:	n/a
39	chr5:147443536-147443586	SK-N-SH	brain:	n/a
40	chr5:147443347-147443397	PANC-1	pancreas:	n/a
41	chr5:147443284-147443334	LNCaP	prostate:	n/a
42	chr5:147443536-147443586	HAEpiC	amniotic membrane:	n/a
43	chr5:147443067-147443117	GM06990	blood:	n/a
44	chr5:147443284-147443334	K562	blood:	n/a
45	chr5:147443252-147443302	RPTEC	kidney:	n/a
46	chr5:147443284-147443334	Caco-2	colon:	n/a
47	chr5:147443284-147443334	AoSMC	blood vessel:	n/a
48	chr5:147443536-147443586	PFSK-1	brain:	n/a
49	chr5:147443252-147443302	HCT-116	colon:	n/a
50	chr5:147443067-147443117	HRCEpiC	kidney:	n/a

No.	Distal block	Cell Line	Cell type
1	chr5:147449509..147451055-chr5:147462616..147464573,2	K562	blood:
2	chr5:147424525..147426952-chr5:147437496..147439638,2	K562	blood:
3	chr5:147424525..147426952-chr5:147437496..147439638,2	K562	blood:
4	chr5:147369292..147371929-chr5:147395160..147396738,2	K562	blood:
5	chr5:147439149..147441922-chr5:147442667..147445001,2	K562	blood:
6	chr16:60919408..60919976-chr5:147395742..147396497,2	MCF-7	breast:

Variant related genes	Relation type
SPINK5	TF binding region
SPINK5	CpG island
ENSG00000133710	chromatin interactions

Extended variants
information (count: 2075 )
Associated
traits (count: 78 )

Variant overlapped rSNPs/rCNVs (count:2075 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs115581458	chr5:147395868-147395869	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs192629331	chr5:147395955-147395956	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs560882582	chr5:147395960-147395961	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs528392192	chr5:147395971-147395972	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs546626524	chr5:147395998-147395999	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs112388249	chr5:147396012-147396013	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs114425913	chr5:147396037-147396038	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs184418786	chr5:147396048-147396049	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs569023017	chr5:147396055-147396056	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs549198353	chr5:147396065-147396066	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs114283017	chr5:147396082-147396083	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs375560692	chr5:147396093-147396094	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs555146359	chr5:147396149-147396150	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs573404361	chr5:147396192-147396193	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs534394101	chr5:147396199-147396200	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs145325753	chr5:147396226-147396227	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs147987215	chr5:147396228-147396229	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs141611495	chr5:147396291-147396292	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs199579616	chr5:147396318-147396319	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs540333987	chr5:147396326-147396327	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs150696011	chr5:147396349-147396350	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs575423085	chr5:147396411-147396412	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs535545670	chr5:147396467-147396468	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs11958263	chr5:147396501-147396502	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs368562178	chr5:147396507-147396508	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs190480368	chr5:147396530-147396531	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs17107596	chr5:147396535-147396536	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs564853962	chr5:147396551-147396552	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs532237303	chr5:147396588-147396589	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs372522319	chr5:147396607-147396608	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs550569429	chr5:147396625-147396626	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs568864503	chr5:147396657-147396658	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs147521468	chr5:147396671-147396672	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs140065656	chr5:147396676-147396677	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs113170498	chr5:147396718-147396719	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs79040273	chr5:147396772-147396773	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs6891750	chr5:147396847-147396848	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs369345502	chr5:147396853-147396854	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs571178240	chr5:147396929-147396930	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs538501648	chr5:147396971-147396972	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs6878056	chr5:147396984-147396985	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs566210082	chr5:147397000-147397001	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs542601218	chr5:147397020-147397021	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs370692124	chr5:147397045-147397046	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs554393906	chr5:147397073-147397074	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs182075581	chr5:147397135-147397136	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs148720761	chr5:147397137-147397138	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs111723790	chr5:147397144-147397145	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs142251314	chr5:147397211-147397212	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs559496229	chr5:147397212-147397213	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:78)

Disease	PMID	Source
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
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	16751803	CNVD
Intellectual disability	22102821	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	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
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
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
Lung cancer	18438408	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	CNVD
Breast cancer	17133270	CNVD
Acute myeloid leukemia	20729466	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Myelodysplastic syndrome	21251322	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Multiple myeloma	17550852	CNVD
Salivary gland tumor	18059337	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Renal cell carcinoma	19377443	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Renal cell carcinoma	18194544	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Renal cell carcinoma	18592004	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Basal cell lymphoma	17053054	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Hyperekplexia	16941485	CNVD
Myelofibrosis	22110671	CNVD
Crohn''s disease	20877625	CNVD
T-cell lymphomas	19863542	CNVD
Breast cancer	17603634	CNVD
early-passage human iPS cells	21368824	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:106 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:147386400-147400000	Weak transcription	HUES6 Cell Line	embryonic stem cell
2	chr5:147388600-147401800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chr5:147391600-147400800	Weak transcription	H9 Cell Line	embryonic stem cell
4	chr5:147391800-147401600	Weak transcription	HUES64 Cell Line	embryonic stem cell
5	chr5:147392600-147396200	Weak transcription	Psoas Muscle	Psoas
6	chr5:147394400-147398600	Weak transcription	Hela-S3	cervix
7	chr5:147394600-147399000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr5:147398600-147400000	Enhancers	Breast Myoepithelial Primary Cells	Breast
9	chr5:147398600-147400600	Enhancers	Hela-S3	cervix
10	chr5:147399000-147399400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr5:147400000-147400400	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
12	chr5:147400200-147400600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr5:147400600-147409800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr5:147411600-147414200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr5:147411600-147414400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
16	chr5:147412200-147412800	Enhancers	iPS-20b Cell Line	embryonic stem cell
17	chr5:147412400-147413000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
18	chr5:147412400-147413200	Enhancers	ES-I3 Cell Line	embryonic stem cell
19	chr5:147412400-147413200	Enhancers	Placenta Amnion	Placenta Amnion
20	chr5:147412400-147413600	Enhancers	NHEK	skin
21	chr5:147412400-147413800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
22	chr5:147412400-147414200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
23	chr5:147412600-147413400	Enhancers	HMEC	breast
24	chr5:147412600-147414000	Enhancers	Hela-S3	cervix
25	chr5:147412800-147413200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
26	chr5:147412800-147413600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
27	chr5:147412800-147418000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
28	chr5:147413200-147413800	Enhancers	Breast Myoepithelial Primary Cells	Breast
29	chr5:147413400-147413800	Enhancers	Placenta	Placenta
30	chr5:147413600-147434200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
31	chr5:147414400-147415400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
32	chr5:147415600-147415800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
33	chr5:147421600-147421800	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr5:147426400-147426600	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
35	chr5:147426600-147433400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
36	chr5:147433400-147436600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
37	chr5:147433400-147439000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr5:147434200-147435000	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
39	chr5:147434800-147436400	ZNF genes & repeats	iPS-18 Cell Line	embryonic stem cell
40	chr5:147435000-147436000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
41	chr5:147435000-147437800	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
42	chr5:147435600-147437800	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
43	chr5:147436000-147436200	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
44	chr5:147436200-147440800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
45	chr5:147436600-147437200	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
46	chr5:147437200-147457400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
47	chr5:147437400-147437600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
48	chr5:147437800-147450200	Weak transcription	HUES64 Cell Line	embryonic stem cell
49	chr5:147437800-147463800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
50	chr5:147439000-147439600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links