Variant report

Variant	nsv541479
Chromosome Location	chr12:38979065-39117868
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	ATF1	chr12:39071567-39071659	K562	blood:	n/a	n/a
2	BATF	chr12:38978987-38979244	GM12878	blood:	n/a	chr12:38979090-38979101
3	BATF	chr12:39099400-39099564	GM12878	blood:	n/a	chr12:39099497-39099506
4	BATF	chr12:38978937-38979254	GM12878	blood:	n/a	chr12:38978975-38978984 chr12:38979090-38979101
5	BRCA1	chr12:38980636-38980915	Hela-S3	cervix:	n/a	n/a
6	BRCA1	chr12:39008036-39008268	GM12878	blood:	n/a	n/a
7	CBX3	chr12:39063333-39063714	K562	blood:	n/a	n/a
8	CCNT2	chr12:39063401-39063641	K562	blood:	n/a	n/a
9	CEBPB	chr12:39022099-39022488	Hela-S3	cervix:	n/a	n/a
10	CEBPB	chr12:39096506-39096527	K562	blood:	n/a	n/a
11	CEBPB	chr12:39104839-39105211	HepG2	liver:	n/a	chr12:39104974-39104985 chr12:39104995-39105006 chr12:39105100-39105111 chr12:39104978-39104989
12	CEBPB	chr12:39036571-39036719	A549	lung:	n/a	n/a
13	CEBPB	chr12:39115180-39115346	HepG2	liver:	n/a	chr12:39115307-39115318
14	CEBPB	chr12:38982717-38983202	ECC-1	luminal epithelium:	n/a	chr12:38982971-38982982
15	CEBPB	chr12:39001091-39001504	Hela-S3	cervix:	n/a	n/a
16	CEBPB	chr12:39022951-39023254	HepG2	liver:	n/a	chr12:39023102-39023113 chr12:39023102-39023115 chr12:39023103-39023114 chr12:39023102-39023115
17	CEBPB	chr12:39058615-39058676	A549	lung:	n/a	n/a
18	CEBPB	chr12:38980443-38981124	Hela-S3	cervix:	n/a	chr12:38980701-38980710 chr12:38980701-38980710 chr12:38980917-38980930 chr12:38980701-38980710 chr12:38980701-38980710 chr12:38980701-38980712
19	CEBPB	chr12:39032394-39032525	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr12:39057555-39057649	HepG2	liver:	n/a	chr12:39057586-39057597
21	CEBPB	chr12:39104828-39105458	Hela-S3	cervix:	n/a	chr12:39104974-39104985 chr12:39104995-39105006 chr12:39105100-39105111 chr12:39104978-39104989
22	CEBPB	chr12:38982837-38983151	H1-hESC	embryonic stem cell:	n/a	chr12:38982971-38982982
23	CEBPB	chr12:39104963-39105137	A549	lung:	n/a	chr12:39104974-39104985 chr12:39104995-39105006 chr12:39105100-39105111 chr12:39104978-39104989
24	CEBPB	chr12:39023027-39023238	K562	blood:	n/a	chr12:39023102-39023113 chr12:39023102-39023115 chr12:39023103-39023114 chr12:39023102-39023115
25	CEBPB	chr12:39071847-39072062	HepG2	liver:	n/a	chr12:39071883-39071894 chr12:39071971-39071980
26	CEBPB	chr12:39022827-39023294	Hela-S3	cervix:	n/a	chr12:39023102-39023113 chr12:39023102-39023115 chr12:39023103-39023114 chr12:39023102-39023115
27	CEBPB	chr12:38982562-38983243	Hela-S3	cervix:	n/a	chr12:38982971-38982982
28	CEBPB	chr12:38982893-38983133	MCF-7	breast:	n/a	chr12:38982971-38982982
29	CEBPB	chr12:39022972-39023196	A549	lung:	n/a	chr12:39023102-39023113 chr12:39023102-39023115 chr12:39023103-39023114 chr12:39023102-39023115
30	CEBPB	chr12:39063374-39063663	K562	blood:	n/a	n/a
31	CEBPB	chr12:38981442-38981823	Hela-S3	cervix:	n/a	n/a
32	CEBPB	chr12:38982828-38983122	HepG2	liver:	n/a	chr12:38982971-38982982
33	CEBPB	chr12:38980570-38980873	A549	lung:	n/a	chr12:38980701-38980710 chr12:38980701-38980710 chr12:38980701-38980710 chr12:38980701-38980710 chr12:38980701-38980712
34	CEBPB	chr12:39115222-39115406	H1-hESC	embryonic stem cell:	n/a	chr12:39115307-39115318
35	CEBPB	chr12:39063418-39063594	K562	blood:	n/a	n/a
36	CEBPB	chr12:39022867-39023227	MCF-7	breast:	n/a	chr12:39023102-39023113 chr12:39023102-39023115 chr12:39023103-39023114 chr12:39023102-39023115
37	CEBPB	chr12:39063350-39063709	K562	blood:	n/a	n/a
38	CEBPB	chr12:38982762-38983190	ECC-1	luminal epithelium:	n/a	chr12:38982971-38982982
39	CHD2	chr12:39104897-39105096	GM12878	blood:	n/a	n/a
40	CHD2	chr12:38980670-38980954	Hela-S3	cervix:	n/a	n/a
41	CHD2	chr12:39007988-39008336	GM12878	blood:	n/a	n/a
42	CTCF	chr12:39058580-39058730	HVMF	connective:	n/a	chr12:39058655-39058671 chr12:39058656-39058677 chr12:39058654-39058672
43	CTCF	chr12:39058640-39058790	RPTEC	kidney:	n/a	chr12:39058655-39058671 chr12:39058656-39058677 chr12:39058654-39058672
44	CTCF	chr12:39058563-39058776	NHEK	skin:	n/a	chr12:39058655-39058671 chr12:39058656-39058677 chr12:39058654-39058672
45	CTCF	chr12:39058441-39058843	H1-hESC	embryonic stem cell:	n/a	chr12:39058655-39058671 chr12:39058656-39058677 chr12:39058654-39058672 chr12:39058821-39058842
46	CTCF	chr12:39058600-39058729	ProgFib	skin:	n/a	chr12:39058655-39058671 chr12:39058656-39058677 chr12:39058654-39058672
47	CTCF	chr12:39058580-39058730	GM12871	blood:	n/a	chr12:39058655-39058671 chr12:39058656-39058677 chr12:39058654-39058672
48	CTCF	chr12:39058500-39058650	HRPEpiC	eye:	n/a	n/a
49	CTCF	chr12:39058552-39058753	T-47D	breast:	n/a	chr12:39058655-39058671 chr12:39058656-39058677 chr12:39058654-39058672
50	CTCF	chr12:39058564-39058770	LNCaP	prostate:	n/a	chr12:39058655-39058671 chr12:39058656-39058677 chr12:39058654-39058672

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:39115589-39115639	CMK	blood:	n/a
2	chr12:39115589-39115639	BJ	skin:	n/a
3	chr12:38984007-38984057	HCM	heart:	n/a
4	chr12:39115661-39115711	K562	blood:	n/a
5	chr12:39115661-39115711	AG10803	skin:	n/a
6	chr12:39115589-39115639	PANC-1	pancreas:	n/a
7	chr12:39115661-39115711	AG04449	skin:	fetal
8	chr12:38984007-38984057	SK-N-SH_RA	brain:	n/a
9	chr12:39115589-39115639	T-47D	breast:	n/a
10	chr12:39115589-39115639	GM12892	blood:	n/a
11	chr12:38984007-38984057	PFSK-1	brain:	n/a
12	chr12:39115589-39115639	PrEC	prostate:	n/a
13	chr12:38984007-38984057	K562	blood:	n/a
14	chr12:38984007-38984057	HRCEpiC	kidney:	n/a
15	chr12:39115661-39115711	ProgFib	skin:	n/a
16	chr12:38984007-38984057	HCF	heart:	n/a
17	chr12:39115661-39115711	GM06990	blood:	n/a
18	chr12:39115661-39115711	HPAEpiC	pulmonary alveolar:	n/a
19	chr12:39115589-39115639	NHBE	bronchial:	n/a
20	chr12:39115589-39115639	HepG2	liver:	n/a
21	chr12:39115661-39115711	SKMC	muscle:	n/a
22	chr12:38984007-38984057	GM12891	blood:	n/a
23	chr12:39115589-39115639	HIPEpiC	eye:	n/a
24	chr12:39115589-39115639	A549	lung:	n/a
25	chr12:39115589-39115639	PFSK-1	brain:	n/a
26	chr12:39115661-39115711	HRE	kidney:	n/a
27	chr12:39115589-39115639	HAEpiC	amniotic membrane:	n/a
28	chr12:39115661-39115711	HNPCEpiC	eye:	n/a
29	chr12:38984007-38984057	HRPEpiC	eye:	n/a
30	chr12:38984007-38984057	HepG2	liver:	n/a
31	chr12:38984007-38984057	SKMC	muscle:	n/a
32	chr12:39115589-39115639	RPTEC	kidney:	n/a
33	chr12:38984007-38984057	HMEC	breast:	n/a
34	chr12:39115589-39115639	AG09319	gingival:	n/a
35	chr12:39115661-39115711	GM19239	blood:	n/a
36	chr12:39115589-39115639	SAEC	small airway:	n/a
37	chr12:39115589-39115639	GM06990	blood:	n/a
38	chr12:39115661-39115711	PFSK-1	brain:	n/a
39	chr12:39115661-39115711	CMK	blood:	n/a
40	chr12:39115589-39115639	Hepatocyte	liver:	n/a
41	chr12:38984007-38984057	IMR90	lung:	fetal
42	chr12:39115661-39115711	NHBE	bronchial:	n/a
43	chr12:38984007-38984057	LNCaP	prostate:	n/a
44	chr12:38984007-38984057	ECC-1	luminal epithelium:	n/a
45	chr12:39115661-39115711	HL-60	blood:	n/a
46	chr12:39115589-39115639	K562	blood:	n/a
47	chr12:38984007-38984057	HUVEC	blood vessel:	n/a
48	chr12:39115661-39115711	GM12892	blood:	n/a
49	chr12:38984007-38984057	U87	brain:	n/a
50	chr12:38984007-38984057	Caco-2	colon:	n/a

No.	Distal block	Cell Line	Cell type
1	chr12:39058333..39059128-chr12:39497120..39498000,2	MCF-7	breast:
2	chr12:39058213..39059596-chr12:39300191..39301086,4	MCF-7	breast:
3	chr12:38990179..38991129-chr4:2331691..2332483,2	Hela-S3	cervix:
4	chr12:39078731..39079461-chr2:68493058..68493608,2	MCF-7	breast:
5	chr10:83534180..83535134-chr12:39026306..39026897,2	HCT-116	colon:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ALG10B-7	chr12:39009229-39009654	NONHSAT027688
2	lnc-ALG10B-7	chr12:39020465-39020542	NONHSAT027688
3	lnc-CPNE8-1	chr12:38983517-38983614	ENSG00000258119
4	lnc-CPNE8-1	chr12:38983517-38983614	XLOC_010050
5	lnc-CPNE8-1	chr12:38983132-38983232	ENSG00000258119
6	lnc-CPNE8-1	chr12:38983132-38983232	XLOC_010050

No.	miRNA target gene	miRNA name	Chromosome Location
1	CPNE8	hsa-miR-30a-5p	chr12:39047301-39047322
2	CPNE8	hsa-miR-124-3p	chr12:39046441-39046460
3	CPNE8	hsa-miR-30a-5p	chr12:39047307-39047300

Variant related genes	Relation type
CPNE8	TF binding region
ENSG00000258119	TF binding region
CPNE8	CpG island
ENSG00000258119	CpG island
ENSG00000257718	chromatin interactions
SLC39A11	miRNA target sites
C1D	miRNA target sites
SLC39A14	miRNA target sites

Extended variants
information (count: 3757 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:3757 , 50 per page) page: 1 2 3 4 5 6 7 ... 76

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs146197323	chr12:38979160-38979161	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs568888705	chr12:38979186-38979187	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs137858926	chr12:38979201-38979202	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs567456975	chr12:38979206-38979207	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs142255851	chr12:38979243-38979244	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs77309825	chr12:38979302-38979303	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs569279244	chr12:38979330-38979331	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs191665253	chr12:38979346-38979347	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs144821308	chr12:38979357-38979358	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs183776310	chr12:38979428-38979429	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs75975395	chr12:38979461-38979462	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs554035771	chr12:38979484-38979485	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs537499662	chr12:38979492-38979493	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs574192407	chr12:38979512-38979513	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs2653752	chr12:38979528-38979529	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs2730944	chr12:38979563-38979564	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs576646158	chr12:38979598-38979599	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs545408805	chr12:38979618-38979619	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs367593831	chr12:38979619-38979620	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs538624526	chr12:38979630-38979631	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs12423659	chr12:38979640-38979641	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs559188239	chr12:38979682-38979683	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs186682611	chr12:38979683-38979684	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs17124758	chr12:38979689-38979690	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs536036494	chr12:38979690-38979691	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs529920392	chr12:38979878-38979879	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs35093272	chr12:38979948-38979949	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs549737617	chr12:38979984-38979985	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs569403395	chr12:38980020-38980021	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs191046409	chr12:38980032-38980033	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs76440175	chr12:38980041-38980042	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs551709468	chr12:38980048-38980049	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs565346029	chr12:38980054-38980055	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs183223393	chr12:38980060-38980061	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs554472826	chr12:38980066-38980067	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs572624355	chr12:38980094-38980095	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs536968255	chr12:38980132-38980133	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs148566012	chr12:38980141-38980142	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs2730938	chr12:38980150-38980151	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs369331997	chr12:38980160-38980161	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs56772240	chr12:38980192-38980193	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs142938297	chr12:38980204-38980205	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs150664372	chr12:38980205-38980206	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs540939873	chr12:38980207-38980208	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs561212974	chr12:38980254-38980255	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs140863653	chr12:38980258-38980259	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs543703173	chr12:38980329-38980330	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs115291508	chr12:38980334-38980335	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs371758173	chr12:38980366-38980367	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs547583193	chr12:38980378-38980379	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:59)

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
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:530 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:38978600-38983200	Enhancers	Hela-S3	cervix
2	chr12:38979200-38979400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr12:38979200-38983200	Enhancers	Primary monocytes fromperipheralblood	blood
4	chr12:38979400-38980400	Enhancers	Monocytes-CD14+_RO01746	blood
5	chr12:38979400-38981200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr12:38980400-38981400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr12:38980400-38982200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
8	chr12:38980600-38982800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
9	chr12:38981000-38981800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chr12:38981200-38981600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
11	chr12:38981200-38981600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr12:38981200-38981600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
13	chr12:38981400-38982600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr12:38981600-38982600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr12:38982200-38983200	Enhancers	Monocytes-CD14+_RO01746	blood
16	chr12:38982600-38982800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
17	chr12:38982600-38982800	Enhancers	Fetal Lung	lung
18	chr12:38982600-38983200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
19	chr12:38982800-38983200	Enhancers	Fetal Kidney	kidney
20	chr12:38995600-38996800	Enhancers	Hela-S3	cervix
21	chr12:39004600-39005200	Enhancers	HUES64 Cell Line	embryonic stem cell
22	chr12:39004800-39005200	Enhancers	iPS-18 Cell Line	embryonic stem cell
23	chr12:39005200-39007800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
24	chr12:39007800-39008200	Enhancers	iPS-18 Cell Line	embryonic stem cell
25	chr12:39012000-39012400	Enhancers	Primary monocytes fromperipheralblood	blood
26	chr12:39017200-39017600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
27	chr12:39017800-39018200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
28	chr12:39018200-39018600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
29	chr12:39018600-39020000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
30	chr12:39019000-39019600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
31	chr12:39022600-39023200	Enhancers	Hela-S3	cervix
32	chr12:39030400-39030800	Enhancers	Esophagus	oesophagus
33	chr12:39030800-39035000	Weak transcription	Esophagus	oesophagus
34	chr12:39031800-39032600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr12:39033000-39034000	Enhancers	Placenta	Placenta
36	chr12:39034000-39034800	Weak transcription	Placenta	Placenta
37	chr12:39035000-39035200	Enhancers	Esophagus	oesophagus
38	chr12:39035200-39035400	Enhancers	Placenta	Placenta
39	chr12:39038800-39041400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
40	chr12:39039200-39039400	Enhancers	Left Ventricle	heart
41	chr12:39039400-39053000	Weak transcription	Left Ventricle	heart
42	chr12:39039600-39039800	Enhancers	Hela-S3	cervix
43	chr12:39039800-39055800	Weak transcription	Hela-S3	cervix
44	chr12:39041000-39041200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr12:39041200-39041800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr12:39041400-39049400	Weak transcription	Primary hematopoietic stem cells	blood
47	chr12:39041800-39043000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr12:39042400-39043200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
49	chr12:39042600-39043200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
50	chr12:39043000-39043400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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