Variant report

Variant	nsv756
Chromosome Location	chr12:67703587-67744743
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:358)
CpG islands
(count:0)
Chromatin interactive
region (count:39)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:4)

(count:358 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr12:67738241-67738268	K562	blood:	n/a	n/a
2	BHLHE40	chr12:67738242-67738441	K562	blood:	n/a	n/a
3	CCNT2	chr12:67721358-67721584	K562	blood:	n/a	n/a
4	CEBPB	chr12:67738242-67738268	K562	blood:	n/a	n/a
5	CHD2	chr12:67718548-67718677	H1-hESC	embryonic stem cell:	n/a	n/a
6	CHD2	chr12:67716214-67717107	H1-hESC	embryonic stem cell:	n/a	n/a
7	CHD2	chr12:67738242-67738268	Hela-S3	cervix:	n/a	n/a
8	CTCF	chr12:67739140-67739290	NHEK	skin:	n/a	chr12:67739258-67739266
9	CTCF	chr12:67708600-67708750	HMF	breast:	n/a	n/a
10	CTCF	chr12:67739220-67739370	NHEK	skin:	n/a	chr12:67739258-67739266
11	CTCF	chr12:67708580-67708730	RPTEC	kidney:	n/a	n/a
12	E2F4	chr12:67710339-67710539	MCF10A-Er-Src	breast:	n/a	n/a
13	E2F6	chr12:67714482-67715041	H1-hESC	embryonic stem cell:	n/a	n/a
14	E2F6	chr12:67715736-67718441	H1-hESC	embryonic stem cell:	n/a	n/a
15	E2F6	chr12:67720254-67720599	H1-hESC	embryonic stem cell:	n/a	n/a
16	EBF1	chr12:67708096-67708219	GM12878	blood:	n/a	n/a
17	ELF1	chr12:67715869-67716112	K562	blood:	n/a	chr12:67715948-67715961
18	FOS	chr12:67708591-67708845	MCF10A-Er-Src	breast:	n/a	n/a
19	FOS	chr12:67714714-67714853	MCF10A-Er-Src	breast:	n/a	n/a
20	FOS	chr12:67714775-67714873	MCF10A-Er-Src	breast:	n/a	n/a
21	FOSL2	chr12:67715965-67716210	HepG2	liver:	n/a	n/a
22	FOSL2	chr12:67713844-67714090	HepG2	liver:	n/a	n/a
23	FOSL2	chr12:67716246-67717663	HepG2	liver:	n/a	n/a
24	GATA3	chr12:67719588-67719773	SH-SY5Y	brain:	n/a	n/a
25	GATA3	chr12:67708075-67708421	SH-SY5Y	brain:	n/a	n/a
26	GATA3	chr12:67723455-67723639	SH-SY5Y	brain:	n/a	chr12:67723555-67723564
27	GTF2F1	chr12:67717514-67717704	Hela-S3	cervix:	n/a	n/a
28	GTF2F1	chr12:67714802-67714957	H1-hESC	embryonic stem cell:	n/a	n/a
29	GTF2F1	chr12:67715178-67715195	H1-hESC	embryonic stem cell:	n/a	n/a
30	GTF2F1	chr12:67715908-67718832	H1-hESC	embryonic stem cell:	n/a	n/a
31	GTF2F1	chr12:67716762-67716820	Hela-S3	cervix:	n/a	n/a
32	GTF2F1	chr12:67719101-67719658	H1-hESC	embryonic stem cell:	n/a	n/a
33	GTF2F1	chr12:67738196-67738269	Hela-S3	cervix:	n/a	n/a
34	HMGN3	chr12:67716390-67716582	K562	blood:	n/a	n/a
35	JUND	chr12:67742277-67742521	HepG2	liver:	n/a	n/a
36	JUND	chr12:67726736-67726971	HepG2	liver:	n/a	n/a
37	KAP1	chr12:67732132-67732664	HEK293	kidney:	n/a	n/a
38	MAFF	chr12:67709742-67709932	HepG2	liver:	n/a	chr12:67709808-67709826
39	MAFF	chr12:67720483-67720789	K562	blood:	n/a	chr12:67720611-67720629
40	MAFF	chr12:67725639-67725992	HepG2	liver:	n/a	chr12:67725802-67725820
41	MAFF	chr12:67705366-67705381	K562	blood:	n/a	n/a
42	MAFF	chr12:67725640-67725975	K562	blood:	n/a	chr12:67725802-67725820
43	MAFF	chr12:67714748-67715083	HepG2	liver:	n/a	chr12:67714901-67714919
44	MAFF	chr12:67714776-67715083	K562	blood:	n/a	chr12:67714901-67714919
45	MAFF	chr12:67720431-67720802	HepG2	liver:	n/a	chr12:67720611-67720629
46	MAFF	chr12:67704721-67704990	HepG2	liver:	n/a	chr12:67704846-67704864
47	MAFF	chr12:67704834-67704837	K562	blood:	n/a	n/a
48	MAFK	chr12:67725643-67725972	Hela-S3	cervix:	n/a	chr12:67725803-67725818 chr12:67725806-67725820 chr12:67725803-67725819 chr12:67725807-67725818 chr12:67725808-67725819 chr12:67725808-67725819 chr12:67725807-67725818
49	MAFK	chr12:67714757-67715085	HepG2	liver:	n/a	chr12:67714903-67714918
50	MAFK	chr12:67704700-67705007	HepG2	liver:	n/a	chr12:67704847-67704862

No data

(count:39 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:67716222..67717888-chr12:67718984..67721962,2	MCF-7	breast:
2	chr12:67681823..67684693-chr12:67719727..67722113,2	K562	blood:
3	chr12:67714913..67718592-chr12:67718971..67722103,3	K562	blood:
4	chr12:67668479..67670313-chr12:67704698..67706848,2	K562	blood:
5	chr12:67713525..67718128-chr12:67719850..67722693,5	MCF-7	breast:
6	chr12:67712478..67714489-chr12:67715652..67718009,2	K562	blood:
7	chr12:67712594..67714797-chr12:132194188..132196961,2	MCF-7	breast:
8	chr12:67708053..67712275-chr12:67717926..67720355,3	K562	blood:
9	chr12:67662013..67664268-chr12:67712332..67714584,2	K562	blood:
10	chr12:67701166..67703768-chr12:67717126..67719527,2	MCF-7	breast:
11	chr12:67662800..67665177-chr12:67715531..67717213,2	MCF-7	breast:
12	chr12:67660883..67663738-chr12:67703241..67705101,2	MCF-7	breast:
13	chr12:67697781..67702337-chr12:67703261..67707738,6	K562	blood:
14	chr12:67712478..67714489-chr12:67715652..67718009,2	K562	blood:
15	chr12:67713525..67718128-chr12:67719850..67722693,5	MCF-7	breast:
16	chr12:67709812..67710332-chr4:99531489..99532009,2	MCF-7	breast:
17	chr12:67708442..67711026-chr12:67711731..67713764,2	MCF-7	breast:
18	chr12:67707079..67709730-chr12:67721053..67723374,2	K562	blood:
19	chr12:67708479..67710797-chr12:67718354..67720777,2	MCF-7	breast:
20	chr12:67716222..67717888-chr12:67718984..67721962,2	MCF-7	breast:
21	chr12:67661690..67663696-chr12:67708706..67710365,2	K562	blood:
22	chr12:67707980..67709583-chr12:67712739..67715234,2	K562	blood:
23	chr12:67707980..67709583-chr12:67712739..67715234,2	K562	blood:
24	chr12:67701153..67702973-chr12:67706397..67708069,2	MCF-7	breast:
25	chr12:67697667..67699390-chr12:67705731..67708067,2	K562	blood:
26	chr12:67662013..67664262-chr12:67712984..67714584,2	K562	blood:
27	chr12:67664539..67666217-chr12:67712484..67714487,2	K562	blood:
28	chr12:67708442..67711026-chr12:67711731..67713764,2	MCF-7	breast:
29	chr12:67714913..67718592-chr12:67718971..67722103,3	K562	blood:
30	chr12:67699472..67703250-chr12:67704428..67707950,5	K562	blood:
31	chr12:67663258..67665425-chr12:67739869..67742001,2	K562	blood:
32	chr12:67708479..67710797-chr12:67718354..67720777,2	MCF-7	breast:
33	chr12:67712989..67715089-chr12:67716509..67719238,2	K562	blood:
34	chr12:67708053..67712275-chr12:67717926..67720355,3	K562	blood:
35	chr12:67661017..67663110-chr12:67715146..67717539,2	K562	blood:
36	chr12:67701166..67703768-chr12:67717126..67719527,2	MCF-7	breast:
37	chr12:67661581..67665640-chr12:67700038..67707681,9	MCF-7	breast:
38	chr12:67712989..67715089-chr12:67716509..67719238,2	K562	blood:
39	chr12:67707079..67709730-chr12:67721053..67723374,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DYRK2-3	chr12:67711527-67713730	ENSG00000247008
2	lnc-DYRK2-3	chr12:67708478-67708952	ENSG00000247008
3	lnc-DYRK2-3	chr12:67711527-67713732	NONHSAT029248

No data

(count:4 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	CAND1	hsa-miR-1	chr12:67707549-67707570
2	CAND1	hsa-miR-186-5p	chr12:67707508-67707528
3	CAND1	hsa-miR-186-5p	chr12:67706949-67706970
4	CAND1	hsa-miR-1	chr12:67707805-67707827

Variant related genes	Relation type
MRPL40P1	TF binding region
ENSG00000111530	chromatin interactions
ENSG00000061936	chromatin interactions
SIPA1L2	miRNA target sites
YWHAH	miRNA target sites

Extended variants
information (count: 1507 )
Associated
traits (count: 89 )

Variant overlapped rSNPs/rCNVs (count:1507 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs139509547	chr12:67703604-67703605	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs574317243	chr12:67703623-67703624	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs149706036	chr12:67703657-67703658	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs368297889	chr12:67703665-67703666	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs372876075	chr12:67703671-67703672	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs61918268	chr12:67703689-67703690	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs201906404	chr12:67703744-67703745	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs149191897	chr12:67703769-67703770	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs145450590	chr12:67703772-67703773	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs367819175	chr12:67703805-67703806	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs199801743	chr12:67703807-67703808	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs371946362	chr12:67703855-67703856	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs377139649	chr12:67703862-67703863	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs116416219	chr12:67703909-67703910	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs531482407	chr12:67703911-67703912	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs184084324	chr12:67703929-67703930	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs374098408	chr12:67703934-67703935	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs558627116	chr12:67703991-67703992	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs375833403	chr12:67704018-67704019	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs561510241	chr12:67704021-67704022	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs369973513	chr12:67704084-67704085	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs189068086	chr12:67704143-67704144	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs547823467	chr12:67704149-67704150	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs139132480	chr12:67704171-67704172	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs73320770	chr12:67704271-67704272	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs529445042	chr12:67704272-67704273	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs570092380	chr12:67704362-67704363	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs537721923	chr12:67704422-67704423	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs193017912	chr12:67704446-67704447	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs567801909	chr12:67704465-67704466	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs370766936	chr12:67704534-67704535	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs73320773	chr12:67704535-67704536	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs553574446	chr12:67704547-67704548	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs143998688	chr12:67704584-67704585	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs146509844	chr12:67704607-67704608	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs572009390	chr12:67704631-67704632	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs543238977	chr12:67704644-67704645	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs113619879	chr12:67704673-67704674	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs34842458	chr12:67704720-67704721	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs141118829	chr12:67704838-67704839	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs115408699	chr12:67704948-67704949	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs374256344	chr12:67705010-67705011	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs386376839	chr12:67705012-67705013	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs71656776	chr12:67705020-67705021	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs200442077	chr12:67705021-67705022	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs200459804	chr12:67705023-67705024	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs115587398	chr12:67705124-67705125	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs117352418	chr12:67705170-67705171	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs116818070	chr12:67705182-67705183	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs11176678	chr12:67705187-67705188	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance

Variant related diseases (count:89)

Disease	PMID	Source
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
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Autism	22495311	CNVD
Neurodevelopmental disorder	22521361	CNVD
T-cell prolymphocytic leukemia	19278963	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
Lung cancer	18438408	CNVD
Breast cancer	17899364	CNVD
Colorectal cancer	16272173	CNVD
Glioblastoma multiforme	17387387	CNVD
liposarcomas	17372913	CNVD
Non-small cell lung cancer	24170126	CNVD
Cancer	16751803	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	21785460	CNVD
small cell lung cancer	20016488	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	21390271	CNVD
Cancer	20164919	CNVD
Leukemia	18628472	CNVD
Fibroblasts	20926602	CNVD
Metanephric adenoma	20802469	CNVD
Follicular lymphoma	18703704	CNVD
Acute myeloid leukemia	21251322	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Mental retardation	17220210	CNVD
Osteopoikilosis	17220210	CNVD
short stature	17220210	CNVD
Burkitt''s lymphoma	20823134	CNVD
abnormal development	18461090	CNVD
Prostate cancer	18632612	CNVD
Ovarian neoplasms	16753589	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	16620391	CNVD
Breast cancer	21364760	CNVD
Urothelial cell carcinoma	18451213	CNVD
Breast cancer	22048815	CNVD
Congenital anomalies of the kidney and urinary tract	21113617	CNVD
Glioblastoma multiforme	22291905	CNVD
Glioblastoma multiforme	19435819	CNVD
Myelofibrosis	22110671	CNVD
Myxofibrosarcoma	16751306	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Lung cancer	17925434	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Disease	21505450	CNVD
craniofacial dysmorphism	21918468	CNVD
Glioblastoma multiforme	21569311	CNVD
Glioblastoma multiforme	19115005	CNVD
Lung adenocarcinoma	17982442	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Bone cancer	16732325	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Breast cancer	17850661	CNVD
Lung cancer	20031968	CNVD
Glioblastoma	17090523	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Breast cancer	17133270	CNVD

Chromatin state (count:534 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:67674600-67708000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr12:67674800-67706400	Weak transcription	Stomach Mucosa	stomach
3	chr12:67681000-67714200	Weak transcription	Spleen	Spleen
4	chr12:67682200-67709000	Strong transcription	Dnd41	blood
5	chr12:67682200-67715200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr12:67682400-67707600	Strong transcription	Primary hematopoietic stem cells short term culture	blood
7	chr12:67682600-67710600	Weak transcription	Right Ventricle	heart
8	chr12:67683400-67710600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr12:67684400-67708400	Strong transcription	GM12878-XiMat	blood
10	chr12:67685800-67708000	Strong transcription	Primary T helper cells fromperipheralblood	blood
11	chr12:67686000-67717000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr12:67686200-67708800	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr12:67686200-67711200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr12:67686200-67716200	Strong transcription	HUES64 Cell Line	embryonic stem cell
15	chr12:67686400-67707800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
16	chr12:67686400-67708800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
17	chr12:67686400-67708800	Strong transcription	Primary B cells from peripheral blood	blood
18	chr12:67686400-67708800	Strong transcription	Rectal Mucosa Donor 31	rectum
19	chr12:67686400-67709000	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
20	chr12:67686400-67709000	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
21	chr12:67686400-67716000	Strong transcription	HUES6 Cell Line	embryonic stem cell
22	chr12:67686600-67708600	Strong transcription	Primary T helper cells PMA-I stimulated	--
23	chr12:67686600-67708800	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
24	chr12:67686600-67708800	Strong transcription	Monocytes-CD14+_RO01746	blood
25	chr12:67686800-67709000	Strong transcription	Primary monocytes fromperipheralblood	blood
26	chr12:67687200-67708600	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
27	chr12:67687600-67708200	Strong transcription	Primary T cells fromperipheralblood	blood
28	chr12:67687600-67708600	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr12:67687600-67708800	Strong transcription	HUES48 Cell Line	embryonic stem cell
30	chr12:67687600-67708800	Strong transcription	Liver	Liver
31	chr12:67687600-67708800	Strong transcription	Rectal Mucosa Donor 29	rectum
32	chr12:67687800-67715400	Strong transcription	iPS-20b Cell Line	embryonic stem cell
33	chr12:67688000-67708400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
34	chr12:67688000-67709000	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
35	chr12:67688200-67711400	Strong transcription	Placenta	Placenta
36	chr12:67688200-67717000	Strong transcription	NH-A	brain
37	chr12:67688400-67716000	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
38	chr12:67688600-67707000	Strong transcription	Primary T cells from cord blood	blood
39	chr12:67688800-67711800	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
40	chr12:67690000-67708800	Strong transcription	Muscle Satellite Cultured Cells	--
41	chr12:67691000-67709400	Strong transcription	HSMM	muscle
42	chr12:67691000-67716000	Weak transcription	Fetal Intestine Small	intestine
43	chr12:67692200-67709200	Strong transcription	A549	lung
44	chr12:67695400-67706400	Weak transcription	Pancreatic Islets	Pancreatic Islet
45	chr12:67695400-67707000	Strong transcription	Primary hematopoietic stem cells	blood
46	chr12:67695400-67708600	Strong transcription	Osteobl	bone
47	chr12:67695400-67709000	Strong transcription	HMEC	breast
48	chr12:67695600-67708800	Strong transcription	HUVEC	blood vessel
49	chr12:67695800-67706600	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
50	chr12:67695800-67707000	Strong transcription	Primary T helper naive cells from peripheral blood	blood

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