Variant report

Variant	nsv976725
Chromosome Location	chr12:123412328-123429898
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:192)
CpG islands
(count:244)
Chromatin interactive
region (count:17)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:192 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:123427273-123427515	HepG2	liver:	n/a	n/a
2	ATF2	chr12:123419107-123419558	GM12878	blood:	n/a	n/a
3	BACH1	chr12:123419515-123419664	K562	blood:	n/a	n/a
4	BACH1	chr12:123427461-123427485	H1-hESC	embryonic stem cell:	n/a	n/a
5	BCLAF1	chr12:123419207-123419646	GM12878	blood:	n/a	n/a
6	BHLHE40	chr12:123427179-123427377	HepG2	liver:	n/a	n/a
7	BHLHE40	chr12:123419257-123419498	GM12878	blood:	n/a	n/a
8	CBX3	chr12:123427159-123427581	K562	blood:	n/a	n/a
9	CEBPB	chr12:123427062-123427411	Hela-S3	cervix:	n/a	n/a
10	CEBPB	chr12:123425846-123426202	Hela-S3	cervix:	n/a	n/a
11	CEBPB	chr12:123422148-123422385	HepG2	liver:	n/a	chr12:123422203-123422214 chr12:123422249-123422262
12	CEBPB	chr12:123422034-123422528	Hela-S3	cervix:	n/a	chr12:123422203-123422214 chr12:123422249-123422262
13	CEBPB	chr12:123417991-123418186	A549	lung:	n/a	chr12:123418150-123418161
14	CEBPB	chr12:123422114-123422416	A549	lung:	n/a	chr12:123422203-123422214 chr12:123422249-123422262
15	CEBPB	chr12:123418089-123418214	HepG2	liver:	n/a	chr12:123418150-123418161
16	CEBPB	chr12:123422202-123422402	K562	blood:	n/a	chr12:123422203-123422214 chr12:123422249-123422262
17	CEBPB	chr12:123418030-123418188	IMR90	lung:	n/a	chr12:123418150-123418161
18	CEBPB	chr12:123422129-123422395	IMR90	lung:	n/a	chr12:123422203-123422214 chr12:123422249-123422262
19	CHD2	chr12:123422227-123422300	Hela-S3	cervix:	n/a	n/a
20	CTCF	chr12:123417674-123417714	Kidney_OC	kidney:	n/a	n/a
21	EBF1	chr12:123422532-123422697	GM12878	blood:	n/a	n/a
22	EGR1	chr12:123419373-123419596	GM12878	blood:	n/a	chr12:123419465-123419479 chr12:123419486-123419500 chr12:123419504-123419518
23	EGR1	chr12:123419335-123419584	K562	blood:	n/a	chr12:123419465-123419479 chr12:123419486-123419500 chr12:123419504-123419518
24	EGR1	chr12:123419365-123419573	K562	blood:	n/a	chr12:123419465-123419479 chr12:123419486-123419500 chr12:123419504-123419518
25	ELF1	chr12:123414158-123414695	GM12878	blood:	n/a	n/a
26	ELK1	chr12:123412293-123412395	GM12878	blood:	n/a	n/a
27	ELK1	chr12:123422264-123422269	Hela-S3	cervix:	n/a	n/a
28	EP300	chr12:123419247-123419503	GM12878	blood:	n/a	n/a
29	EP300	chr12:123419247-123419553	GM12878	blood:	n/a	n/a
30	EP300	chr12:123422370-123422567	GM12878	blood:	n/a	n/a
31	EP300	chr12:123422134-123422519	Hela-S3	cervix:	n/a	chr12:123422250-123422264
32	EP300	chr12:123422440-123422712	GM12878	blood:	n/a	n/a
33	EP300	chr12:123427099-123427445	HepG2	liver:	n/a	n/a
34	EP300	chr12:123429125-123429497	T-47D	breast:	n/a	n/a
35	FOS	chr12:123429185-123429513	MCF10A-Er-Src	breast:	n/a	chr12:123429223-123429230
36	FOS	chr12:123422123-123422441	MCF10A-Er-Src	breast:	n/a	n/a
37	FOS	chr12:123429275-123429511	MCF10A-Er-Src	breast:	n/a	n/a
38	FOS	chr12:123425958-123426317	MCF10A-Er-Src	breast:	n/a	n/a
39	FOS	chr12:123429204-123429511	MCF10A-Er-Src	breast:	n/a	chr12:123429223-123429230
40	FOS	chr12:123422116-123422463	MCF10A-Er-Src	breast:	n/a	n/a
41	FOS	chr12:123422104-123422631	MCF10A-Er-Src	breast:	n/a	n/a
42	FOS	chr12:123425964-123426316	MCF10A-Er-Src	breast:	n/a	n/a
43	FOS	chr12:123425968-123426231	MCF10A-Er-Src	breast:	n/a	n/a
44	FOS	chr12:123422127-123422583	MCF10A-Er-Src	breast:	n/a	n/a
45	FOS	chr12:123425961-123426317	MCF10A-Er-Src	breast:	n/a	n/a
46	FOSL1	chr12:123427148-123427459	K562	blood:	n/a	n/a
47	FOSL2	chr12:123429180-123429582	A549	lung:	n/a	chr12:123429223-123429230
48	FOSL2	chr12:123427053-123427472	HepG2	liver:	n/a	chr12:123427292-123427303
49	FOSL2	chr12:123427038-123427527	HepG2	liver:	n/a	chr12:123427292-123427303
50	FOXA1	chr12:123427188-123427516	HepG2	liver:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:123414607-123414657	AG04449	skin:	fetal
2	chr12:123414345-123414395	SKMC	muscle:	n/a
3	chr12:123414345-123414395	ProgFib	skin:	n/a
4	chr12:123414638-123414688	SK-N-SH	brain:	n/a
5	chr12:123414556-123414606	HCPEpiC	choroid plexus:	n/a
6	chr12:123414345-123414395	ECC-1	luminal epithelium:	n/a
7	chr12:123414638-123414688	NB4	blood:	n/a
8	chr12:123414638-123414688	HUVEC	blood vessel:	n/a
9	chr12:123414345-123414395	Caco-2	colon:	n/a
10	chr12:123414638-123414688	IMR90	lung:	fetal
11	chr12:123414556-123414606	HNPCEpiC	eye:	n/a
12	chr12:123414556-123414606	Hepatocyte	liver:	n/a
13	chr12:123414345-123414395	HAEpiC	amniotic membrane:	n/a
14	chr12:123414638-123414688	GM12891	blood:	n/a
15	chr12:123414638-123414688	ProgFib	skin:	n/a
16	chr12:123414607-123414657	ovcar-3	ovarian:	n/a
17	chr12:123414638-123414688	HL-60	blood:	n/a
18	chr12:123414607-123414657	Caco-2	colon:	n/a
19	chr12:123414607-123414657	BE2_C	brain:	n/a
20	chr12:123414638-123414688	CMK	blood:	n/a
21	chr12:123414607-123414657	MCF10A-Er-Src	breast:	n/a
22	chr12:123414638-123414688	HMEC	breast:	n/a
23	chr12:123414607-123414657	BJ	skin:	n/a
24	chr12:123414638-123414688	AG04450	lung:	fetal
25	chr12:123414607-123414657	AG09319	gingival:	n/a
26	chr12:123414607-123414657	SK-N-SH_RA	brain:	n/a
27	chr12:123414345-123414395	CMK	blood:	n/a
28	chr12:123414607-123414657	A549	lung:	n/a
29	chr12:123414556-123414606	HCT-116	colon:	n/a
30	chr12:123414607-123414657	ProgFib	skin:	n/a
31	chr12:123414638-123414688	H1-hESC	embryonic stem cell:	embryo
32	chr12:123414556-123414606	HEEpiC	esophagus:	n/a
33	chr12:123414607-123414657	T-47D	breast:	n/a
34	chr12:123414607-123414657	RPTEC	kidney:	n/a
35	chr12:123414556-123414606	ovcar-3	ovarian:	n/a
36	chr12:123414345-123414395	HL-60	blood:	n/a
37	chr12:123414607-123414657	GM19239	blood:	n/a
38	chr12:123414607-123414657	HEEpiC	esophagus:	n/a
39	chr12:123414345-123414395	GM12892	blood:	n/a
40	chr12:123414607-123414657	MCF-7	breast:	n/a
41	chr12:123414345-123414395	HRPEpiC	eye:	n/a
42	chr12:123414638-123414688	NH-A	brain:	n/a
43	chr12:123414607-123414657	HepG2	liver:	n/a
44	chr12:123414345-123414395	HNPCEpiC	eye:	n/a
45	chr12:123414345-123414395	GM12878	blood:	n/a
46	chr12:123414638-123414688	PANC-1	pancreas:	n/a
47	chr12:123414345-123414395	MCF10A-Er-Src	breast:	n/a
48	chr12:123414638-123414688	LNCaP	prostate:	n/a
49	chr12:123414556-123414606	AoSMC	blood vessel:	n/a
50	chr12:123414556-123414606	PFSK-1	brain:	n/a

(count:17 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:123406897..123409663-chr12:123410616..123413101,2	K562	blood:
2	chr12:123426745..123429433-chr12:123432536..123436941,4	K562	blood:
3	chr12:123379519..123381901-chr12:123420925..123423638,2	MCF-7	breast:
4	chr12:123409186..123412265-chr12:123414114..123415906,3	K562	blood:
5	chr12:123415535..123420026-chr12:123422545..123426280,4	K562	blood:
6	chr12:123424712..123426973-chr12:123428403..123431628,3	K562	blood:
7	chr12:123428831..123431560-chr12:123448558..123451555,2	K562	blood:
8	chr12:123427499..123429140-chr12:123435163..123436941,2	K562	blood:
9	chr12:123404141..123406851-chr12:123412530..123414179,2	K562	blood:
10	chr12:123418526..123420273-chr12:123424780..123426394,2	K562	blood:
11	chr12:123413568..123415277-chr12:123423150..123425253,2	K562	blood:
12	chr12:123418526..123420273-chr12:123424780..123426394,2	K562	blood:
13	chr12:123428831..123432471-chr12:123448558..123452277,3	K562	blood:
14	chr12:123413568..123415277-chr12:123423150..123425253,2	K562	blood:
15	chr12:123415535..123420026-chr12:123422545..123426280,4	K562	blood:
16	chr12:123424761..123427438-chr12:123430033..123431700,2	K562	blood:
17	chr12:123409356..123412001-chr12:123418941..123421663,2	K562	blood:

No data

Variant related genes	Relation type
ABCB9	TF binding region
ABCB9	CpG island
ENSG00000139722	chromatin interactions
ENSG00000150967	chromatin interactions

Extended variants
information (count: 627 )
Associated
traits (count: 72 )

Variant overlapped rSNPs/rCNVs (count:627 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs536490424	chr12:123412328-123412329	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs188212759	chr12:123412356-123412357	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs573512158	chr12:123412365-123412366	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs540594135	chr12:123412390-123412391	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs565246655	chr12:123412417-123412418	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs575276911	chr12:123412426-123412427	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs73408832	chr12:123412443-123412444	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs544669152	chr12:123412518-123412519	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs181003452	chr12:123412563-123412564	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs530715624	chr12:123412590-123412591	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs549231979	chr12:123412673-123412674	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs35123523	chr12:123412680-123412681	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs60739634	chr12:123412742-123412743	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs185668493	chr12:123412744-123412745	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs546587631	chr12:123412754-123412755	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs571175557	chr12:123412771-123412772	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs58283587	chr12:123412797-123412798	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs550253747	chr12:123412849-123412850	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs568648696	chr12:123412941-123412942	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs76030876	chr12:123413032-123413033	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs536429756	chr12:123413038-123413039	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs373691634	chr12:123413061-123413062	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs555119679	chr12:123413119-123413120	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs375764546	chr12:123413204-123413205	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs149525854	chr12:123413207-123413208	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs188862782	chr12:123413213-123413214	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs373805613	chr12:123413229-123413230	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs7133420	chr12:123413231-123413232	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs4080877	chr12:123413311-123413312	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
30	rs371022398	chr12:123413327-123413328	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs181448785	chr12:123413355-123413356	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs544657008	chr12:123413381-123413382	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs562953479	chr12:123413412-123413413	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs575014141	chr12:123413477-123413478	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs116769166	chr12:123413478-123413479	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs186799115	chr12:123413487-123413488	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs192143618	chr12:123413505-123413506	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs2343682	chr12:123413596-123413597	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs528277108	chr12:123413673-123413674	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs114585376	chr12:123413740-123413741	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs565075778	chr12:123413743-123413744	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs531967468	chr12:123413756-123413757	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs550190762	chr12:123413765-123413766	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs568537091	chr12:123413766-123413767	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs3896872	chr12:123413778-123413779	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs149267580	chr12:123413894-123413895	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs574780996	chr12:123413905-123413906	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs368205336	chr12:123413930-123413931	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs372006478	chr12:123413931-123413932	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs372474579	chr12:123413963-123413964	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:72)

Disease	PMID	Source
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
T-cell prolymphocytic leukemia	19278963	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
small cell lung cancer	20016488	CNVD
Glioblastoma multiforme	21390271	CNVD
Cancer	20164919	CNVD
Cancer	16751803	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Wilms tumour	21544195	CNVD
Ovarian cancer	21720365	CNVD
Colorectal cancer	16272173	CNVD
lymphocytic leukemia	21291569	CNVD
Breast cancer	16397240	CNVD
Breast cancer	17133270	CNVD
Breast cancer	17603634	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Schizophrenia	18923514	CNVD
Schizophrenia	22241247	CNVD
Cryptorchidism	21048976	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Neuroblastoma	18923191	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	21806811	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Prostate cancer	18632612	CNVD
Myelofibrosis	22110671	CNVD
Beckwith-Wiedemann syndrome	20648245	CNVD
Developmental delay	21457577	CNVD
dysmorphic	21457577	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Olfactory neuroblastoma	18408657	CNVD
Chordoma	18071362	CNVD
Ependymoma	20639864	CNVD
Pancreatic cancer	17952125	CNVD
head and neck squamous cell carcinoma	24351288	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:576 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:123401400-123417200	Weak transcription	Osteobl	bone
2	chr12:123401400-123425200	Weak transcription	Esophagus	oesophagus
3	chr12:123401400-123426000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
4	chr12:123402600-123416400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr12:123402600-123429200	Weak transcription	Placenta Amnion	Placenta Amnion
6	chr12:123402800-123414000	Weak transcription	Brain Cingulate Gyrus	brain
7	chr12:123402800-123414200	Weak transcription	Ovary	ovary
8	chr12:123402800-123414600	Weak transcription	Brain Hippocampus Middle	brain
9	chr12:123402800-123415400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
10	chr12:123402800-123416400	Weak transcription	Brain Substantia Nigra	brain
11	chr12:123402800-123426600	Weak transcription	NHLF	lung
12	chr12:123402800-123429200	Weak transcription	Gastric	stomach
13	chr12:123402800-123430800	Weak transcription	Duodenum Smooth Muscle	Duodenum
14	chr12:123403000-123413800	Weak transcription	Pancreas	Pancrea
15	chr12:123403000-123414200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr12:123403000-123414200	Weak transcription	Brain Angular Gyrus	brain
17	chr12:123403000-123414400	Weak transcription	Right Ventricle	heart
18	chr12:123403000-123416600	Weak transcription	Stomach Smooth Muscle	stomach
19	chr12:123403000-123426400	Weak transcription	Left Ventricle	heart
20	chr12:123403000-123428800	Weak transcription	Lung	lung
21	chr12:123403000-123444200	Weak transcription	Aorta	Aorta
22	chr12:123403400-123414200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
23	chr12:123403400-123427000	Weak transcription	A549	lung
24	chr12:123403600-123413200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
25	chr12:123405200-123416800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
26	chr12:123405200-123424800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
27	chr12:123405200-123428600	Weak transcription	NHEK	skin
28	chr12:123405400-123414000	Weak transcription	Fetal Intestine Small	intestine
29	chr12:123406800-123414200	Weak transcription	Fetal Stomach	stomach
30	chr12:123406800-123415200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
31	chr12:123406800-123417000	Weak transcription	Fetal Lung	lung
32	chr12:123406800-123419800	Weak transcription	Skeletal Muscle Male	skeletal muscle
33	chr12:123406800-123426600	Weak transcription	Rectal Mucosa Donor 29	rectum
34	chr12:123408600-123413800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
35	chr12:123408600-123414200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
36	chr12:123408800-123414200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
37	chr12:123409200-123412800	Enhancers	GM12878-XiMat	blood
38	chr12:123409200-123413400	Enhancers	Primary B cells from peripheral blood	blood
39	chr12:123409400-123413800	Weak transcription	Brain Anterior Caudate	brain
40	chr12:123409400-123427600	Weak transcription	Rectal Mucosa Donor 31	rectum
41	chr12:123409800-123413400	Weak transcription	Fetal Brain Female	brain
42	chr12:123410000-123413000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
43	chr12:123410000-123414000	Weak transcription	Brain Inferior Temporal Lobe	brain
44	chr12:123410000-123414600	Weak transcription	Brain Germinal Matrix	brain
45	chr12:123410200-123413200	Enhancers	Primary B cells from cord blood	blood
46	chr12:123410400-123413400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
47	chr12:123410800-123412600	Enhancers	Placenta	Placenta
48	chr12:123411200-123412400	Enhancers	Primary hematopoietic stem cells short term culture	blood
49	chr12:123411200-123412800	Enhancers	Primary monocytes fromperipheralblood	blood
50	chr12:123411200-123412800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood

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