Variant report

Variant	esv13329
Chromosome Location	chr12:123178106-123210671
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:486)
CpG islands
(count:733)
Chromatin interactive
region (count:9)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:486 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:123205566-123205898	HepG2	liver:	n/a	n/a
2	ARID3A	chr12:123201358-123201518	HepG2	liver:	n/a	n/a
3	ATF1	chr12:123210635-123210977	K562	blood:	n/a	n/a
4	ATF2	chr12:123210466-123210885	GM12878	blood:	n/a	n/a
5	ATF2	chr12:123210410-123211094	GM12878	blood:	n/a	n/a
6	ATF2	chr12:123204895-123205418	GM12878	blood:	n/a	n/a
7	ATF2	chr12:123209037-123209549	GM12878	blood:	n/a	n/a
8	ATF2	chr12:123205558-123206155	GM12878	blood:	n/a	n/a
9	ATF2	chr12:123204789-123205408	GM12878	blood:	n/a	n/a
10	ATF2	chr12:123205629-123206088	GM12878	blood:	n/a	n/a
11	BATF	chr12:123210530-123210866	GM12878	blood:	n/a	n/a
12	BATF	chr12:123205671-123206135	GM12878	blood:	n/a	n/a
13	BATF	chr12:123205543-123206143	GM12878	blood:	n/a	n/a
14	BATF	chr12:123209199-123209452	GM12878	blood:	n/a	n/a
15	BATF	chr12:123203568-123203966	GM12878	blood:	n/a	n/a
16	BATF	chr12:123210498-123210895	GM12878	blood:	n/a	n/a
17	BATF	chr12:123205050-123205325	GM12878	blood:	n/a	chr12:123205161-123205169
18	BATF	chr12:123198415-123198667	GM12878	blood:	n/a	n/a
19	BATF	chr12:123184951-123185203	GM12878	blood:	n/a	n/a
20	BATF	chr12:123198368-123198752	GM12878	blood:	n/a	n/a
21	BATF	chr12:123203623-123203925	GM12878	blood:	n/a	n/a
22	BATF	chr12:123204957-123205419	GM12878	blood:	n/a	chr12:123205161-123205169
23	BATF	chr12:123184904-123185288	GM12878	blood:	n/a	n/a
24	BCL11A	chr12:123198389-123198642	GM12878	blood:	n/a	chr12:123198604-123198613
25	BCL11A	chr12:123184925-123185178	GM12878	blood:	n/a	chr12:123185140-123185149
26	BCL11A	chr12:123210605-123210791	GM12878	blood:	n/a	n/a
27	BCL11A	chr12:123210575-123210904	GM12878	blood:	n/a	n/a
28	BCL11A	chr12:123204972-123205414	GM12878	blood:	n/a	n/a
29	BCL11A	chr12:123205656-123206061	GM12878	blood:	n/a	chr12:123205903-123205912 chr12:123205904-123205913
30	BCL3	chr12:123205716-123206048	GM12878	blood:	n/a	chr12:123205903-123205912 chr12:123205904-123205913
31	BCL3	chr12:123204901-123205335	GM12878	blood:	n/a	n/a
32	BCLAF1	chr12:123204694-123205409	GM12878	blood:	n/a	n/a
33	BCLAF1	chr12:123210420-123210976	GM12878	blood:	n/a	n/a
34	BCLAF1	chr12:123209100-123209784	GM12878	blood:	n/a	n/a
35	BCLAF1	chr12:123205600-123206137	GM12878	blood:	n/a	chr12:123205903-123205912 chr12:123205904-123205913
36	BHLHE40	chr12:123210534-123210860	GM12878	blood:	n/a	n/a
37	BHLHE40	chr12:123205681-123206131	GM12878	blood:	n/a	n/a
38	BHLHE40	chr12:123210652-123210840	K562	blood:	n/a	n/a
39	CBX3	chr12:123210454-123211278	HCT-116	colon:	n/a	n/a
40	CBX3	chr12:123192855-123193151	K562	blood:	n/a	n/a
41	CCNT2	chr12:123210602-123210819	K562	blood:	n/a	n/a
42	CEBPB	chr12:123192198-123192210	H1-hESC	embryonic stem cell:	n/a	n/a
43	CEBPB	chr12:123192061-123192396	A549	lung:	n/a	chr12:123192205-123192216
44	CEBPB	chr12:123194984-123195338	MCF-7	breast:	n/a	n/a
45	CEBPB	chr12:123201328-123201540	A549	lung:	n/a	n/a
46	CEBPB	chr12:123192060-123192294	HepG2	liver:	n/a	chr12:123192205-123192216
47	CEBPB	chr12:123187833-123188233	Hela-S3	cervix:	n/a	n/a
48	CEBPB	chr12:123201306-123201554	HepG2	liver:	n/a	n/a
49	CEBPB	chr12:123205020-123205301	IMR90	lung:	n/a	chr12:123205169-123205182
50	CEBPB	chr12:123192059-123192377	IMR90	lung:	n/a	chr12:123192205-123192216

(count:733 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:123200353-123200403	PANC-1	pancreas:	n/a
2	chr12:123200353-123200403	PANC-1	pancreas:	n/a
3	chr12:123189256-123189306	H1-hESC	embryonic stem cell:	embryo
4	chr12:123200353-123200403	Jurkat	blood:	n/a
5	chr12:123201372-123201422	AG09319	gingival:	n/a
6	chr12:123187474-123187524	AG09319	gingival:	n/a
7	chr12:123201189-123201239	PrEC	prostate:	n/a
8	chr12:123187474-123187524	HRE	kidney:	n/a
9	chr12:123201362-123201412	NHDF-neo	bronchial:	n/a
10	chr12:123200953-123201003	HRCEpiC	kidney:	n/a
11	chr12:123189236-123189286	GM12891	blood:	n/a
12	chr12:123188078-123188128	HCF	heart:	n/a
13	chr12:123187474-123187524	HEK293	kidney:	embryo
14	chr12:123188078-123188128	HL-60	blood:	n/a
15	chr12:123187474-123187524	A549	lung:	n/a
16	chr12:123188078-123188128	SK-N-SH_RA	brain:	n/a
17	chr12:123200533-123200583	Jurkat	blood:	n/a
18	chr12:123200953-123201003	PFSK-1	brain:	n/a
19	chr12:123187474-123187524	AG09309	skin:	n/a
20	chr12:123200533-123200583	H1-hESC	embryonic stem cell:	embryo
21	chr12:123189256-123189306	GM12891	blood:	n/a
22	chr12:123201372-123201422	GM12892	blood:	n/a
23	chr12:123187474-123187524	HIPEpiC	eye:	n/a
24	chr12:123201362-123201412	Hepatocyte	liver:	n/a
25	chr12:123201362-123201412	HNPCEpiC	eye:	n/a
26	chr12:123187529-123187579	GM12891	blood:	n/a
27	chr12:123200533-123200583	HCM	heart:	n/a
28	chr12:123189236-123189286	MCF-7	breast:	n/a
29	chr12:123201189-123201239	HRPEpiC	eye:	n/a
30	chr12:123200353-123200403	H1-hESC	embryonic stem cell:	embryo
31	chr12:123201189-123201239	GM12892	blood:	n/a
32	chr12:123187073-123187123	U87	brain:	n/a
33	chr12:123189256-123189306	ovcar-3	ovarian:	n/a
34	chr12:123201362-123201412	HEK293	kidney:	embryo
35	chr12:123201372-123201422	MCF10A-Er-Src	breast:	n/a
36	chr12:123189236-123189286	HPAEpiC	pulmonary alveolar:	n/a
37	chr12:123201189-123201239	AG09319	gingival:	n/a
38	chr12:123187529-123187579	K562	blood:	n/a
39	chr12:123201189-123201239	GM06990	blood:	n/a
40	chr12:123201362-123201412	A549	lung:	n/a
41	chr12:123200353-123200403	HRPEpiC	eye:	n/a
42	chr12:123189256-123189306	PFSK-1	brain:	n/a
43	chr12:123187529-123187579	HCPEpiC	choroid plexus:	n/a
44	chr12:123201372-123201422	HNPCEpiC	eye:	n/a
45	chr12:123200533-123200583	GM06990	blood:	n/a
46	chr12:123187529-123187579	ECC-1	luminal epithelium:	n/a
47	chr12:123201362-123201412	T-47D	breast:	n/a
48	chr12:123201372-123201422	IMR90	lung:	fetal
49	chr12:123201372-123201422	K562	blood:	n/a
50	chr12:123187529-123187579	Caco-2	colon:	n/a

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:123205952..123207948-chr12:123213167..123215455,2	K562	blood:
2	chr12:123201536..123203616-chr12:123208338..123210644,2	MCF-7	breast:
3	chr12:123186486..123188573-chr12:123199930..123201817,2	MCF-7	breast:
4	chr12:123204275..123207099-chr12:123214252..123216398,2	MCF-7	breast:
5	chr12:123201536..123203616-chr12:123208338..123210644,2	MCF-7	breast:
6	chr12:123186486..123188573-chr12:123199930..123201817,2	MCF-7	breast:
7	chr12:123204711..123206759-chr12:123209537..123212379,2	MCF-7	breast:
8	chr12:123171777..123173769-chr12:123177481..123180099,2	MCF-7	breast:
9	chr12:123210591..123212657-chr12:123213454..123215681,5	MCF-7	breast:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DENR-2	chr12:123198838-123199340	ENSG00000256249
2	lnc-HCAR3-1	chr12:123210623-123211051	ENSG00000270134.1
3	lnc-DENR-2	chr12:123200008-123200255	ENSG00000256249
4	lnc-DENR-2	chr12:123199801-123200187	NONHSAT031529
5	lnc-DENR-2	chr12:123185843-123186416	NONHSAT031529

No data

Variant related genes	Relation type
HCAR3	TF binding region
ENSG00000256249	TF binding region
HCAR2	TF binding region
HCAR3	CpG island
ENSG00000256249	CpG island
HCAR2	CpG island
ENSG00000255398	chromatin interactions
ENSG00000196917	chromatin interactions
ENSG00000270134	chromatin interactions
ENSG00000182782	chromatin interactions
LRRC41	miRNA target sites
GALNT11	miRNA target sites

Extended variants
information (count: 1529 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:1529 , 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	rs563786611	chr12:123178114-123178115	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs75134921	chr12:123178134-123178135	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs138780624	chr12:123178208-123178209	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs561852517	chr12:123178218-123178219	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs371204119	chr12:123178262-123178263	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs4759361	chr12:123178280-123178281	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs34740659	chr12:123178304-123178305	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs187721391	chr12:123178308-123178309	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs12816033	chr12:123178332-123178333	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs533509838	chr12:123178340-123178341	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs149386957	chr12:123178353-123178354	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs12824485	chr12:123178356-123178357	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs12816060	chr12:123178372-123178373	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs491489	chr12:123178410-123178411	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs201413578	chr12:123178478-123178479	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs77162017	chr12:123178479-123178480	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs537066442	chr12:123178541-123178542	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs549329570	chr12:123178558-123178559	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs567891281	chr12:123178574-123178575	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs192338765	chr12:123178608-123178609	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs573055844	chr12:123178669-123178670	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs553192729	chr12:123178685-123178686	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs142318959	chr12:123178709-123178710	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs545358076	chr12:123178713-123178714	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs115656760	chr12:123178723-123178724	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs183162516	chr12:123178739-123178740	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs557580105	chr12:123178742-123178743	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs576056059	chr12:123178768-123178769	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs543075690	chr12:123178774-123178775	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs632393	chr12:123178817-123178818	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs573890387	chr12:123178848-123178849	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs541328274	chr12:123178849-123178850	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs631955	chr12:123178911-123178912	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs530805926	chr12:123178939-123178940	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs147328736	chr12:123178956-123178957	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs141064232	chr12:123178993-123178994	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs113480700	chr12:123178994-123178995	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs375506504	chr12:123179045-123179046	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs549144874	chr12:123179079-123179080	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs187103629	chr12:123179125-123179126	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs191871951	chr12:123179127-123179128	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs546892848	chr12:123179142-123179143	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs571570326	chr12:123179225-123179226	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs538864317	chr12:123179276-123179277	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs557505534	chr12:123179284-123179285	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs369594137	chr12:123179307-123179308	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs576087960	chr12:123179342-123179343	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs537906602	chr12:123179369-123179370	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs537138121	chr12:123179381-123179382	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs35210073	chr12:123179382-123179383	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:68)

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

Chromatin state (count:427 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:123166600-123187800	Weak transcription	A549	lung
2	chr12:123174000-123199800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
3	chr12:123176400-123182000	Weak transcription	Adipose Nuclei	Adipose
4	chr12:123176400-123182400	Weak transcription	Primary neutrophils fromperipheralblood	blood
5	chr12:123177400-123178200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr12:123177600-123179200	Enhancers	HUVEC	blood vessel
7	chr12:123178200-123181000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr12:123180600-123182400	Weak transcription	Monocytes-CD14+_RO01746	blood
9	chr12:123181000-123181800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr12:123181200-123182200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr12:123181200-123182400	Enhancers	Placenta	Placenta
12	chr12:123181200-123183000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
13	chr12:123181200-123183000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
14	chr12:123181600-123182600	Enhancers	ES-I3 Cell Line	embryonic stem cell
15	chr12:123181600-123182600	Enhancers	HMEC	breast
16	chr12:123181600-123182600	Enhancers	NHEK	skin
17	chr12:123181800-123185400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
18	chr12:123182000-123182600	Enhancers	Adipose Nuclei	Adipose
19	chr12:123182200-123184200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr12:123182400-123182600	Enhancers	Monocytes-CD14+_RO01746	blood
21	chr12:123182400-123182800	Enhancers	Primary neutrophils fromperipheralblood	blood
22	chr12:123182400-123182800	Weak transcription	Placenta	Placenta
23	chr12:123182400-123183000	Enhancers	Primary T cells from cord blood	blood
24	chr12:123182600-123183800	Weak transcription	Monocytes-CD14+_RO01746	blood
25	chr12:123182600-123185200	Weak transcription	Adipose Nuclei	Adipose
26	chr12:123182600-123185200	Weak transcription	HMEC	breast
27	chr12:123182600-123185400	Weak transcription	NHEK	skin
28	chr12:123182800-123183000	Enhancers	Placenta	Placenta
29	chr12:123182800-123185200	Weak transcription	Primary neutrophils fromperipheralblood	blood
30	chr12:123183000-123185000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
31	chr12:123183000-123185200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
32	chr12:123183000-123185400	Weak transcription	Placenta	Placenta
33	chr12:123183800-123184800	Enhancers	Monocytes-CD14+_RO01746	blood
34	chr12:123184000-123188800	Enhancers	Primary monocytes fromperipheralblood	blood
35	chr12:123184200-123185800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
36	chr12:123184800-123185200	Weak transcription	Monocytes-CD14+_RO01746	blood
37	chr12:123185000-123185400	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
38	chr12:123185200-123185400	Active TSS	Adipose Nuclei	Adipose
39	chr12:123185200-123185800	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
40	chr12:123185200-123186000	Active TSS	Primary neutrophils fromperipheralblood	blood
41	chr12:123185200-123186000	Enhancers	HMEC	breast
42	chr12:123185200-123186000	Enhancers	Monocytes-CD14+_RO01746	blood
43	chr12:123185200-123187200	Active TSS	Esophagus	oesophagus
44	chr12:123185400-123185600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
45	chr12:123185400-123185600	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
46	chr12:123185400-123185600	Flanking Active TSS	Adipose Nuclei	Adipose
47	chr12:123185400-123185600	Enhancers	Placenta	Placenta
48	chr12:123185400-123185600	Flanking Active TSS	NHEK	skin
49	chr12:123185400-123186200	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
50	chr12:123185400-123186800	Active TSS	Primary hematopoietic stem cells	blood

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