Variant report

Variant	nsv826349
Chromosome Location	chr12:41878846-41911495
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:236)
CpG islands
(count:122)
Chromatin interactive
region (count:4)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:236 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr12:41878944-41879485	GM12878	blood:	n/a	n/a
2	ATF2	chr12:41879026-41879416	GM12878	blood:	n/a	n/a
3	BATF	chr12:41879007-41879359	GM12878	blood:	n/a	chr12:41879199-41879208
4	BATF	chr12:41878971-41879408	GM12878	blood:	n/a	chr12:41879199-41879208
5	BCL11A	chr12:41878996-41879379	GM12878	blood:	n/a	n/a
6	BCL3	chr12:41879059-41879351	GM12878	blood:	n/a	n/a
7	BCL3	chr12:41879062-41879374	GM12878	blood:	n/a	n/a
8	BRCA1	chr12:41881960-41881989	GM12878	blood:	n/a	n/a
9	CEBPB	chr12:41903087-41903913	ECC-1	luminal epithelium:	n/a	chr12:41903196-41903209
10	CEBPB	chr12:41888705-41888963	A549	lung:	n/a	chr12:41888820-41888829 chr12:41888818-41888829 chr12:41888842-41888854 chr12:41888820-41888831 chr12:41888818-41888831
11	CEBPB	chr12:41888712-41888990	IMR90	lung:	n/a	chr12:41888820-41888829 chr12:41888818-41888829 chr12:41888842-41888854 chr12:41888820-41888831 chr12:41888818-41888831
12	CEBPB	chr12:41888675-41888967	H1-hESC	embryonic stem cell:	n/a	chr12:41888820-41888829 chr12:41888818-41888829 chr12:41888842-41888854 chr12:41888820-41888831 chr12:41888818-41888831
13	CEBPB	chr12:41903094-41903932	ECC-1	luminal epithelium:	n/a	chr12:41903196-41903209
14	CEBPB	chr12:41888684-41888976	HepG2	liver:	n/a	chr12:41888820-41888829 chr12:41888818-41888829 chr12:41888842-41888854 chr12:41888820-41888831 chr12:41888818-41888831
15	CTCF	chr12:41908820-41908970	GM12869	blood:	n/a	n/a
16	CTCF	chr12:41908857-41908965	GM13977	blood:	n/a	n/a
17	CTCF	chr12:41908744-41909052	GM12878	blood:	n/a	n/a
18	CTCF	chr12:41908896-41908910	MCF-7	breast:	n/a	n/a
19	CTCF	chr12:41908820-41908970	GM12875	blood:	n/a	n/a
20	CTCF	chr12:41908780-41908930	HPAF	blood vessel:	n/a	n/a
21	CTCF	chr12:41908900-41909050	NHDF-neo	bronchial:	n/a	n/a
22	CTCF	chr12:41908840-41908990	AG09319	gingival:	n/a	n/a
23	CTCF	chr12:41908820-41908970	GM12878	blood:	n/a	n/a
24	CTCF	chr12:41908780-41908930	GM12867	blood:	n/a	n/a
25	CTCF	chr12:41908800-41908950	NHLF	lung:	n/a	n/a
26	CTCF	chr12:41908840-41908990	GM12873	blood:	n/a	n/a
27	CTCF	chr12:41908860-41909010	SK-N-SH_RA	brain:	n/a	n/a
28	CTCF	chr12:41908860-41909010	HPF	lung:	n/a	n/a
29	CTCF	chr12:41908822-41908987	GM19238	blood:	n/a	n/a
30	CTCF	chr12:41908800-41908950	Caco-2	colon:	n/a	n/a
31	CTCF	chr12:41908820-41908970	HUVEC	blood vessel:	n/a	n/a
32	CTCF	chr12:41908840-41908990	HMEC	breast:	n/a	n/a
33	CTCF	chr12:41908860-41909010	GM12872	blood:	n/a	n/a
34	CTCF	chr12:41908820-41908970	HPF	lung:	n/a	n/a
35	CTCF	chr12:41908780-41908930	HRPEpiC	eye:	n/a	n/a
36	CTCF	chr12:41908825-41908976	A549	lung:	n/a	n/a
37	CTCF	chr12:41908820-41908970	HVMF	connective:	n/a	n/a
38	CTCF	chr12:41908740-41908890	AG04450	lung:	n/a	n/a
39	CTCF	chr12:41908820-41908970	HFF-Myc	foreskin:	n/a	n/a
40	CTCF	chr12:41908858-41908935	MCF-7	breast:	n/a	n/a
41	CTCF	chr12:41908820-41908970	GM12872	blood:	n/a	n/a
42	CTCF	chr12:41908820-41908970	GM12871	blood:	n/a	n/a
43	CTCF	chr12:41908639-41909106	SK-N-SH	brain:	n/a	n/a
44	CTCF	chr12:41908820-41908970	HCPEpiC	choroid plexus:	n/a	n/a
45	CTCF	chr12:41908800-41908950	AG04449	skin:	n/a	n/a
46	CTCF	chr12:41908900-41909050	RPTEC	kidney:	n/a	n/a
47	CTCF	chr12:41908800-41908950	GM12873	blood:	n/a	n/a
48	CTCF	chr12:41908800-41908950	GM12864	blood:	n/a	n/a
49	CTCF	chr12:41908767-41909007	H1-hESC	embryonic stem cell:	n/a	n/a
50	CTCF	chr12:41908812-41908980	GM12891	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:41902312-41902362	GM12878	blood:	n/a
2	chr12:41902312-41902362	SK-N-MC	brain:	n/a
3	chr12:41902309-41902359	Hela-S3	cervix:	n/a
4	chr12:41902312-41902362	GM06990	blood:	n/a
5	chr12:41902309-41902359	HAEpiC	amniotic membrane:	n/a
6	chr12:41902309-41902359	U87	brain:	n/a
7	chr12:41902312-41902362	Hepatocyte	liver:	n/a
8	chr12:41902309-41902359	ProgFib	skin:	n/a
9	chr12:41902309-41902359	HCM	heart:	n/a
10	chr12:41902312-41902362	HCM	heart:	n/a
11	chr12:41902312-41902362	NHDF-neo	bronchial:	n/a
12	chr12:41902312-41902362	AG10803	skin:	n/a
13	chr12:41902309-41902359	H1-hESC	embryonic stem cell:	embryo
14	chr12:41902309-41902359	LNCaP	prostate:	n/a
15	chr12:41902309-41902359	NT2-D1	testis:	n/a
16	chr12:41902312-41902362	ECC-1	luminal epithelium:	n/a
17	chr12:41902309-41902359	AG04450	lung:	fetal
18	chr12:41902312-41902362	Caco-2	colon:	n/a
19	chr12:41902309-41902359	NHBE	bronchial:	n/a
20	chr12:41902309-41902359	Jurkat	blood:	n/a
21	chr12:41902312-41902362	MCF-7	breast:	n/a
22	chr12:41902312-41902362	HPAEpiC	pulmonary alveolar:	n/a
23	chr12:41902312-41902362	Hela-S3	cervix:	n/a
24	chr12:41902312-41902362	IMR90	lung:	fetal
25	chr12:41902312-41902362	HCF	heart:	n/a
26	chr12:41902312-41902362	HRE	kidney:	n/a
27	chr12:41902312-41902362	CMK	blood:	n/a
28	chr12:41902309-41902359	AG09309	skin:	n/a
29	chr12:41902312-41902362	AG09319	gingival:	n/a
30	chr12:41902309-41902359	HUVEC	blood vessel:	n/a
31	chr12:41902309-41902359	NB4	blood:	n/a
32	chr12:41902312-41902362	SK-N-SH_RA	brain:	n/a
33	chr12:41902309-41902359	HRPEpiC	eye:	n/a
34	chr12:41902309-41902359	HCF	heart:	n/a
35	chr12:41902312-41902362	LNCaP	prostate:	n/a
36	chr12:41902309-41902359	PFSK-1	brain:	n/a
37	chr12:41902309-41902359	MCF-7	breast:	n/a
38	chr12:41902309-41902359	MCF10A-Er-Src	breast:	n/a
39	chr12:41902312-41902362	SKMC	muscle:	n/a
40	chr12:41902309-41902359	NHDF-neo	bronchial:	n/a
41	chr12:41902309-41902359	SK-N-SH	brain:	n/a
42	chr12:41902309-41902359	HepG2	liver:	n/a
43	chr12:41902312-41902362	HepG2	liver:	n/a
44	chr12:41902309-41902359	SAEC	small airway:	n/a
45	chr12:41902309-41902359	HPAEpiC	pulmonary alveolar:	n/a
46	chr12:41902309-41902359	A549	lung:	n/a
47	chr12:41902312-41902362	BE2_C	brain:	n/a
48	chr12:41902312-41902362	HEK293	kidney:	embryo
49	chr12:41902312-41902362	PANC-1	pancreas:	n/a
50	chr12:41902312-41902362	K562	blood:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr12:41903994..41905628-chr12:41905672..41908634,2	K562	blood:
2	chr12:41895577..41896459-chr17:58519980..58520506,2	MCF-7	breast:
3	chr12:41903994..41905628-chr12:41905672..41908634,2	K562	blood:
4	chr12:41866420..41869255-chr12:41877018..41879768,2	K562	blood:

No data

Variant related genes	Relation type
PDZRN4	TF binding region
PDZRN4	CpG island
ENSG00000257228	chromatin interactions

Extended variants
information (count: 1299 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:1299 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs560226378	chr12:41878856-41878857	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs527388269	chr12:41878892-41878893	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs77745274	chr12:41878900-41878901	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs564478314	chr12:41878917-41878918	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs150626144	chr12:41878931-41878932	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs550027222	chr12:41878957-41878958	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs568138327	chr12:41879011-41879012	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs535486080	chr12:41879036-41879037	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs547459492	chr12:41879064-41879065	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs566211219	chr12:41879065-41879066	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs539500901	chr12:41879117-41879118	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs558726622	chr12:41879119-41879120	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs577077373	chr12:41879191-41879192	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs538158006	chr12:41879232-41879233	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs556522417	chr12:41879240-41879241	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs574766343	chr12:41879246-41879247	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs541847688	chr12:41879334-41879335	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs559892775	chr12:41879379-41879380	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs558098280	chr12:41879388-41879389	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs572111558	chr12:41879464-41879465	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs545543042	chr12:41879479-41879480	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs564720915	chr12:41879483-41879484	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs73130651	chr12:41879492-41879493	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs377275506	chr12:41879517-41879518	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs79152064	chr12:41879575-41879576	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs562080071	chr12:41879671-41879672	Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs529535069	chr12:41879688-41879689	Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs112324667	chr12:41879695-41879696	Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs549661201	chr12:41879703-41879704	Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs547771253	chr12:41879742-41879743	Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs116314702	chr12:41879819-41879820	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs17129388	chr12:41879821-41879822	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs541304073	chr12:41879843-41879844	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs186300890	chr12:41879850-41879851	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs551555635	chr12:41879851-41879852	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs568053296	chr12:41879880-41879881	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs11180951	chr12:41879903-41879904	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs369742736	chr12:41879930-41879931	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs556383203	chr12:41879937-41879938	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs150144630	chr12:41879941-41879942	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs547278264	chr12:41879983-41879984	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs183028425	chr12:41879995-41879996	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs111750969	chr12:41880012-41880013	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs199716317	chr12:41880020-41880021	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs11180952	chr12:41880044-41880045	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs529133404	chr12:41880066-41880067	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs138859504	chr12:41880099-41880100	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs578233323	chr12:41880118-41880119	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs146340011	chr12:41880229-41880230	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs187656013	chr12:41880234-41880235	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:57)

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
Neurodevelopmental disorder	22521361	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
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
Breast cancer	21364760	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Cancer	20164919	CNVD

Chromatin state (count:181 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:41869600-41905200	Weak transcription	Colon Smooth Muscle	Colon
2	chr12:41877400-41903600	Weak transcription	Ovary	ovary
3	chr12:41878400-41879000	Enhancers	HUVEC	blood vessel
4	chr12:41878800-41879200	Enhancers	Right Atrium	heart
5	chr12:41878800-41879400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
6	chr12:41879000-41879200	Flanking Active TSS	GM12878-XiMat	blood
7	chr12:41879000-41879200	Enhancers	HMEC	breast
8	chr12:41879000-41879600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr12:41879000-41879800	Flanking Active TSS	HUVEC	blood vessel
10	chr12:41879200-41879400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
11	chr12:41879200-41879400	Active TSS	GM12878-XiMat	blood
12	chr12:41879200-41880200	Weak transcription	HMEC	breast
13	chr12:41879400-41880400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
14	chr12:41879600-41880000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr12:41879800-41881200	Enhancers	HUVEC	blood vessel
16	chr12:41880000-41880400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
17	chr12:41880200-41880600	Enhancers	HMEC	breast
18	chr12:41880400-41880800	Enhancers	iPS-20b Cell Line	embryonic stem cell
19	chr12:41880400-41880800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
20	chr12:41880400-41880800	Bivalent Enhancer	Aorta	Aorta
21	chr12:41880600-41881200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
22	chr12:41880600-41881800	Enhancers	Brain Germinal Matrix	brain
23	chr12:41881800-41887000	Weak transcription	Brain Germinal Matrix	brain
24	chr12:41886200-41887400	Enhancers	Brain Anterior Caudate	brain
25	chr12:41886200-41887400	Enhancers	Brain Substantia Nigra	brain
26	chr12:41886200-41891800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr12:41886600-41887000	Active TSS	Brain Hippocampus Middle	brain
28	chr12:41886600-41887800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr12:41887000-41887200	Flanking Active TSS	Brain Hippocampus Middle	brain
30	chr12:41887000-41887800	Enhancers	Brain Germinal Matrix	brain
31	chr12:41887200-41887600	Enhancers	Brain Hippocampus Middle	brain
32	chr12:41887400-41887600	Flanking Active TSS	Brain Substantia Nigra	brain
33	chr12:41887400-41888400	Weak transcription	Brain Anterior Caudate	brain
34	chr12:41887600-41901400	Weak transcription	Brain Substantia Nigra	brain
35	chr12:41887800-41893600	Weak transcription	Brain Germinal Matrix	brain
36	chr12:41888000-41891400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
37	chr12:41888400-41888800	Enhancers	Brain Anterior Caudate	brain
38	chr12:41888400-41889000	Enhancers	ES-I3 Cell Line	embryonic stem cell
39	chr12:41888600-41889000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
40	chr12:41889000-41890000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
41	chr12:41889600-41890400	Enhancers	Psoas Muscle	Psoas
42	chr12:41890000-41890200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
43	chr12:41890000-41890600	Enhancers	HUVEC	blood vessel
44	chr12:41890200-41890800	Enhancers	Skeletal Muscle Male	skeletal muscle
45	chr12:41890400-41895200	Weak transcription	Psoas Muscle	Psoas
46	chr12:41891000-41891600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
47	chr12:41891200-41891600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
48	chr12:41891400-41893400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
49	chr12:41891800-41893400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr12:41893400-41894000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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