Variant report

Variant	nsv899011
Chromosome Location	chr12:39517706-39594506
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	ATF2	chr12:39567647-39567934	GM12878	blood:	n/a	n/a
2	ATF2	chr12:39567500-39567998	GM12878	blood:	n/a	n/a
3	ATF3	chr12:39521167-39521657	HCT-116	colon:	n/a	n/a
4	BACH1	chr12:39538915-39539530	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr12:39549702-39549727	K562	blood:	n/a	n/a
6	BATF	chr12:39567534-39567895	GM12878	blood:	n/a	chr12:39567715-39567725 chr12:39567718-39567729
7	BATF	chr12:39567520-39567922	GM12878	blood:	n/a	chr12:39567715-39567725 chr12:39567718-39567729
8	BRCA1	chr12:39523080-39523089	GM12878	blood:	n/a	n/a
9	CBX3	chr12:39521170-39521643	HCT-116	colon:	n/a	n/a
10	CBX3	chr12:39521134-39521689	HCT-116	colon:	n/a	n/a
11	CEBPB	chr12:39532943-39533193	HepG2	liver:	n/a	chr12:39533031-39533042
12	CEBPB	chr12:39533001-39533112	A549	lung:	n/a	chr12:39533031-39533042
13	CEBPB	chr12:39538527-39538582	H1-hESC	embryonic stem cell:	n/a	n/a
14	CEBPB	chr12:39521252-39521523	A549	lung:	n/a	n/a
15	CEBPB	chr12:39539314-39539516	H1-hESC	embryonic stem cell:	n/a	n/a
16	CEBPB	chr12:39551906-39552084	A549	lung:	n/a	n/a
17	CEBPB	chr12:39532883-39533173	H1-hESC	embryonic stem cell:	n/a	chr12:39533031-39533042
18	CEBPB	chr12:39532810-39533191	A549	lung:	n/a	chr12:39533031-39533042
19	CEBPB	chr12:39521105-39521738	HCT-116	colon:	n/a	n/a
20	CEBPB	chr12:39530489-39530807	HepG2	liver:	n/a	chr12:39530637-39530648
21	CEBPB	chr12:39530527-39530806	IMR90	lung:	n/a	chr12:39530637-39530648
22	CEBPB	chr12:39521164-39521642	HCT-116	colon:	n/a	n/a
23	CEBPB	chr12:39521214-39521541	Hela-S3	cervix:	n/a	n/a
24	CEBPB	chr12:39562110-39562176	A549	lung:	n/a	chr12:39562117-39562128 chr12:39562117-39562126 chr12:39562117-39562126 chr12:39562117-39562126 chr12:39562117-39562126 chr12:39562115-39562128 chr12:39562115-39562128
25	CEBPB	chr12:39521239-39521591	A549	lung:	n/a	n/a
26	CREB1	chr12:39539135-39539569	A549	lung:	n/a	n/a
27	CTCF	chr12:39539340-39539490	HVMF	connective:	n/a	chr12:39539378-39539387
28	CTCF	chr12:39578286-39578377	MCF-7	breast:	n/a	n/a
29	CTCF	chr12:39539320-39539470	GM12878	blood:	n/a	chr12:39539378-39539387
30	CTCF	chr12:39582756-39582819	GM20000	blood:	n/a	n/a
31	CTCF	chr12:39539020-39539170	HEEpiC	esophagus:	n/a	chr12:39539144-39539154 chr12:39539143-39539156
32	CTCF	chr12:39539180-39539330	GM12867	blood:	n/a	n/a
33	CTCF	chr12:39539340-39539490	HBMEC	blood vessel:	n/a	chr12:39539378-39539387
34	CTCF	chr12:39539320-39539470	HPAF	blood vessel:	n/a	chr12:39539378-39539387
35	CTCF	chr12:39539270-39539514	GM20000	blood:	n/a	chr12:39539378-39539387
36	CTCF	chr12:39539264-39539512	Fibrobl	skin:	n/a	chr12:39539378-39539387
37	CTCF	chr12:39539217-39539537	NHEK	skin:	n/a	chr12:39539523-39539536 chr12:39539378-39539387
38	CTCF	chr12:39539200-39539350	HFF-Myc	foreskin:	n/a	n/a
39	CTCF	chr12:39539246-39539492	Pancreas_OC	pancreas:	n/a	chr12:39539378-39539387
40	CTCF	chr12:39539320-39539470	GM12874	blood:	n/a	chr12:39539378-39539387
41	CTCF	chr12:39539280-39539430	GM06990	blood:	n/a	chr12:39539378-39539387
42	CTCF	chr12:39539121-39539627	A549	lung:	n/a	chr12:39539523-39539536 chr12:39539144-39539154 chr12:39539378-39539387 chr12:39539143-39539156
43	CTCF	chr12:39539400-39539550	HA-sp	spinal cord:	n/a	chr12:39539523-39539536
44	CTCF	chr12:39539300-39539450	GM12875	blood:	n/a	chr12:39539378-39539387
45	CTCF	chr12:39539340-39539490	GM12868	blood:	n/a	chr12:39539378-39539387
46	CTCF	chr12:39539300-39539450	GM12878	blood:	n/a	chr12:39539378-39539387
47	CTCF	chr12:39539180-39539330	HCM	heart:	n/a	n/a
48	CTCF	chr12:39539263-39539510	Lung_OC	lung:	n/a	chr12:39539378-39539387
49	CTCF	chr12:39539240-39539390	RPTEC	kidney:	n/a	chr12:39539378-39539387
50	CTCF	chr12:39539340-39539490	HA-sp	spinal cord:	n/a	chr12:39539378-39539387

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:39539558-39539608	RPTEC	kidney:	n/a
2	chr12:39535355-39535405	HPAEpiC	pulmonary alveolar:	n/a
3	chr12:39538106-39538156	SAEC	small airway:	n/a
4	chr12:39539558-39539608	AG04449	skin:	fetal
5	chr12:39538854-39538904	T-47D	breast:	n/a
6	chr12:39538604-39538654	NHDF-neo	bronchial:	n/a
7	chr12:39538854-39538904	HNPCEpiC	eye:	n/a
8	chr12:39538106-39538156	HUVEC	blood vessel:	n/a
9	chr12:39539408-39539458	AG04450	lung:	fetal
10	chr12:39538604-39538654	NT2-D1	testis:	n/a
11	chr12:39539408-39539458	HNPCEpiC	eye:	n/a
12	chr12:39538106-39538156	Hela-S3	cervix:	n/a
13	chr12:39538106-39538156	Caco-2	colon:	n/a
14	chr12:39538106-39538156	HAEpiC	amniotic membrane:	n/a
15	chr12:39539422-39539472	Caco-2	colon:	n/a
16	chr12:39538604-39538654	AG09309	skin:	n/a
17	chr12:39538854-39538904	SK-N-MC	brain:	n/a
18	chr12:39539558-39539608	NT2-D1	testis:	n/a
19	chr12:39538940-39538990	ovcar-3	ovarian:	n/a
20	chr12:39539558-39539608	Hepatocyte	liver:	n/a
21	chr12:39538106-39538156	NHBE	bronchial:	n/a
22	chr12:39538940-39538990	ECC-1	luminal epithelium:	n/a
23	chr12:39538940-39538990	HIPEpiC	eye:	n/a
24	chr12:39539408-39539458	NHDF-neo	bronchial:	n/a
25	chr12:39535355-39535405	NT2-D1	testis:	n/a
26	chr12:39539422-39539472	PrEC	prostate:	n/a
27	chr12:39538854-39538904	Caco-2	colon:	n/a
28	chr12:39538604-39538654	CMK	blood:	n/a
29	chr12:39538940-39538990	AG09309	skin:	n/a
30	chr12:39539408-39539458	AG09319	gingival:	n/a
31	chr12:39535355-39535405	GM12878	blood:	n/a
32	chr12:39538854-39538904	NHBE	bronchial:	n/a
33	chr12:39538940-39538990	NHDF-neo	bronchial:	n/a
34	chr12:39539408-39539458	IMR90	lung:	fetal
35	chr12:39539408-39539458	T-47D	breast:	n/a
36	chr12:39539408-39539458	MCF10A-Er-Src	breast:	n/a
37	chr12:39539558-39539608	MCF10A-Er-Src	breast:	n/a
38	chr12:39538940-39538990	AG09319	gingival:	n/a
39	chr12:39538854-39538904	HRE	kidney:	n/a
40	chr12:39535355-39535405	Caco-2	colon:	n/a
41	chr12:39538940-39538990	LNCaP	prostate:	n/a
42	chr12:39538940-39538990	NHBE	bronchial:	n/a
43	chr12:39538604-39538654	HCF	heart:	n/a
44	chr12:39535355-39535405	GM19239	blood:	n/a
45	chr12:39538940-39538990	Hela-S3	cervix:	n/a
46	chr12:39539422-39539472	HAEpiC	amniotic membrane:	n/a
47	chr12:39538940-39538990	HRPEpiC	eye:	n/a
48	chr12:39538604-39538654	Hela-S3	cervix:	n/a
49	chr12:39538106-39538156	HCM	heart:	n/a
50	chr12:39535355-39535405	NB4	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr12:39523769..39526109-chr12:39527144..39529582,2	K562	blood:
2	chr12:39546903..39548495-chr12:39550724..39552270,2	K562	blood:
3	chr12:39523769..39526109-chr12:39527144..39529582,2	K562	blood:
4	chr12:39582358..39584719-chr20:55839448..55841740,2	MCF-7	breast:
5	chr12:39546903..39548495-chr12:39550724..39552270,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C12orf40-5	chr12:39564448-39564682	NONHSAT027697

Variant related genes	Relation type
ENSG00000270718	TF binding region
ENSG00000270718	CpG island
ENSG00000101144	chromatin interactions

Extended variants
information (count: 1160 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:1160 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10783619	chr12:39517706-39517707	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs139909689	chr12:39517709-39517710	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs539514573	chr12:39517710-39517711	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs574288372	chr12:39517715-39517716	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs370579603	chr12:39517743-39517744	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs143337324	chr12:39517749-39517750	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs564971938	chr12:39517774-39517775	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs144505853	chr12:39517789-39517790	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs531804856	chr12:39517915-39517916	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs11170798	chr12:39517951-39517952	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs183232314	chr12:39517962-39517963	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs527759631	chr12:39517963-39517964	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs539540139	chr12:39518004-39518005	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs547828367	chr12:39518005-39518006	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs398019181	chr12:39518020-39518021	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs115486987	chr12:39518058-39518059	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs534462790	chr12:39518074-39518075	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs148416145	chr12:39518088-39518089	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs549803359	chr12:39518103-39518104	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs189664322	chr12:39518109-39518110	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs142517318	chr12:39518154-39518155	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs558281480	chr12:39518168-39518169	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs150929523	chr12:39518169-39518170	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs534377674	chr12:39518176-39518177	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs552226060	chr12:39518190-39518191	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs1463209	chr12:39518293-39518294	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
27	rs574350212	chr12:39518294-39518295	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs543348772	chr12:39518314-39518315	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs141909984	chr12:39518331-39518332	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs145641118	chr12:39518344-39518345	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs545640280	chr12:39518353-39518354	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs565445471	chr12:39518391-39518392	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs113059796	chr12:39518392-39518393	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs527821627	chr12:39518405-39518406	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs182103075	chr12:39518414-39518415	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs188068604	chr12:39518524-39518525	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs147728706	chr12:39518626-39518627	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs142553794	chr12:39518638-39518639	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs79314427	chr12:39518656-39518657	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs569853834	chr12:39518657-39518658	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs532406179	chr12:39518690-39518691	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs150238175	chr12:39518703-39518704	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs191241832	chr12:39518728-39518729	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs534461480	chr12:39518734-39518735	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs554237170	chr12:39518748-39518749	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs568108976	chr12:39518785-39518786	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs79748215	chr12:39518863-39518864	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs574473243	chr12:39518864-39518865	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs140669064	chr12:39518893-39518894	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs183478709	chr12:39518901-39518902	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:60)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
Seminomas	18059402	CNVD
Wilms tumour	21544195	CNVD
Esophageal cancer	21851588	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Ewing''s sarcoma	21437220	CNVD
Testicular germ cell tumor	18059402	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Ewing''s sarcoma	17952124	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Cancer	20164919	CNVD
Neurodevelopmental disorder	22521361	CNVD
Breast cancer	21509527	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Renal cell carcinoma	18194544	CNVD
Breast cancer	21949216	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21637783	CNVD
Glioblastoma multiforme	21080181	CNVD
Renal cell carcinoma	19461508	CNVD
Burkitt''s lymphoma	18698080	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	17603634	CNVD
Cancer	21183584	CNVD
Hirschsprung''s Disease	21712996	CNVD
Lissencephaly	21572526	CNVD
Lung cancer	18438408	CNVD
Acute myeloid leukemia	21251322	CNVD
small cell lung cancer	20016488	CNVD
Autism	20858243	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Breast cancer	19602461	CNVD
Breast cancer	17899364	CNVD
Cancer	20164920	CNVD
Colorectal cancer	16272173	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:315 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:39515800-39519600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr12:39516000-39518200	Enhancers	H1 Cell Line	embryonic stem cell
3	chr12:39516000-39518400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr12:39516000-39518600	Enhancers	iPS-15b Cell Line	embryonic stem cell
5	chr12:39516000-39519600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr12:39516000-39519600	Enhancers	Placenta	Placenta
7	chr12:39516200-39517800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr12:39516200-39517800	Enhancers	HMEC	breast
9	chr12:39516200-39519800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr12:39516400-39518000	Enhancers	Placenta Amnion	Placenta Amnion
11	chr12:39516400-39518400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr12:39516400-39518600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
13	chr12:39516400-39518600	Enhancers	NHEK	skin
14	chr12:39516600-39517800	Enhancers	H9 Cell Line	embryonic stem cell
15	chr12:39516600-39517800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
16	chr12:39516600-39518400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr12:39516600-39519600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
18	chr12:39516800-39519400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
19	chr12:39517000-39518200	Weak transcription	HUES48 Cell Line	embryonic stem cell
20	chr12:39517000-39518600	Enhancers	HUVEC	blood vessel
21	chr12:39517000-39518800	Enhancers	ES-I3 Cell Line	embryonic stem cell
22	chr12:39517000-39523000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
23	chr12:39517200-39518200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
24	chr12:39517400-39518800	Enhancers	HUES6 Cell Line	embryonic stem cell
25	chr12:39517400-39523000	Weak transcription	HUES64 Cell Line	embryonic stem cell
26	chr12:39517600-39517800	Enhancers	iPS-18 Cell Line	embryonic stem cell
27	chr12:39517800-39518200	Weak transcription	H9 Cell Line	embryonic stem cell
28	chr12:39517800-39519200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
29	chr12:39517800-39519200	Weak transcription	HMEC	breast
30	chr12:39517800-39523200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
31	chr12:39518200-39518400	Weak transcription	H1 Cell Line	embryonic stem cell
32	chr12:39518200-39518400	Enhancers	H9 Cell Line	embryonic stem cell
33	chr12:39518200-39518800	Enhancers	HUES48 Cell Line	embryonic stem cell
34	chr12:39518200-39519600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
35	chr12:39518400-39518800	Enhancers	H1 Cell Line	embryonic stem cell
36	chr12:39518400-39521200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
37	chr12:39518400-39521400	Weak transcription	H9 Cell Line	embryonic stem cell
38	chr12:39518400-39523000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
39	chr12:39518600-39519000	Weak transcription	NHEK	skin
40	chr12:39518600-39519600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
41	chr12:39518600-39520800	Weak transcription	HUVEC	blood vessel
42	chr12:39518800-39523000	Weak transcription	HUES48 Cell Line	embryonic stem cell
43	chr12:39519000-39519800	Enhancers	NHEK	skin
44	chr12:39519200-39519400	Enhancers	HMEC	breast
45	chr12:39519200-39519600	Enhancers	Sigmoid Colon	Sigmoid Colon
46	chr12:39519200-39519800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
47	chr12:39519400-39519600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
48	chr12:39519400-39519600	Genic enhancers	HMEC	breast
49	chr12:39519600-39519800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
50	chr12:39519600-39521000	Weak transcription	HMEC	breast

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