Variant report

Variant	nsv557478
Chromosome Location	chr12:10604945-10698255
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:362)
CpG islands
(count:429)
Chromatin interactive
region (count:5)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:362 , 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	ARID3A	chr12:10653777-10653877	K562	blood:	n/a	n/a
2	ATF2	chr12:10695883-10696624	GM12878	blood:	n/a	n/a
3	ATF2	chr12:10693081-10694102	GM12878	blood:	n/a	n/a
4	ATF2	chr12:10695894-10696491	GM12878	blood:	n/a	n/a
5	ATF2	chr12:10693152-10694036	GM12878	blood:	n/a	n/a
6	BATF	chr12:10696061-10696446	GM12878	blood:	n/a	n/a
7	BATF	chr12:10641882-10642185	GM12878	blood:	n/a	chr12:10642014-10642025
8	BATF	chr12:10696036-10696487	GM12878	blood:	n/a	n/a
9	BATF	chr12:10693317-10693939	GM12878	blood:	n/a	chr12:10693650-10693661
10	BATF	chr12:10693300-10693868	GM12878	blood:	n/a	chr12:10693650-10693661
11	BATF	chr12:10641906-10642182	GM12878	blood:	n/a	chr12:10642014-10642025
12	BCL11A	chr12:10693310-10693858	GM12878	blood:	n/a	n/a
13	BCL11A	chr12:10696076-10696426	GM12878	blood:	n/a	n/a
14	BCL11A	chr12:10693354-10693625	GM12878	blood:	n/a	n/a
15	BCL11A	chr12:10671811-10671985	GM12878	blood:	n/a	n/a
16	BCL11A	chr12:10696199-10696390	GM12878	blood:	n/a	n/a
17	BCL3	chr12:10693360-10693849	GM12878	blood:	n/a	n/a
18	BCL3	chr12:10696031-10696586	GM12878	blood:	n/a	n/a
19	BCL3	chr12:10695995-10696628	GM12878	blood:	n/a	n/a
20	BCL3	chr12:10693210-10693959	GM12878	blood:	n/a	n/a
21	BCLAF1	chr12:10696071-10696445	GM12878	blood:	n/a	n/a
22	BCLAF1	chr12:10693241-10693808	GM12878	blood:	n/a	n/a
23	BCLAF1	chr12:10693217-10694044	GM12878	blood:	n/a	n/a
24	BHLHE40	chr12:10693305-10693679	GM12878	blood:	n/a	n/a
25	BRCA1	chr12:10676248-10676302	GM12878	blood:	n/a	n/a
26	CBX3	chr12:10608263-10608767	HCT-116	colon:	n/a	n/a
27	CEBPB	chr12:10675319-10675536	HepG2	liver:	n/a	chr12:10675436-10675447
28	CEBPB	chr12:10605885-10606198	A549	lung:	n/a	chr12:10606038-10606049
29	CEBPB	chr12:10675342-10675509	A549	lung:	n/a	chr12:10675436-10675447
30	CEBPB	chr12:10693180-10693997	GM12878	blood:	n/a	n/a
31	CEBPB	chr12:10605854-10606222	Hela-S3	cervix:	n/a	chr12:10606038-10606049
32	CEBPB	chr12:10695688-10696520	GM12878	blood:	n/a	n/a
33	CEBPB	chr12:10605878-10606169	IMR90	lung:	n/a	chr12:10606038-10606049
34	CEBPB	chr12:10605864-10606214	HepG2	liver:	n/a	chr12:10606038-10606049
35	CREB1	chr12:10693316-10693819	GM12878	blood:	n/a	n/a
36	CREB1	chr12:10693203-10694090	GM12878	blood:	n/a	n/a
37	CREB1	chr12:10674190-10674624	GM12878	blood:	n/a	n/a
38	CTCF	chr12:10653740-10653890	HCPEpiC	choroid plexus:	n/a	n/a
39	CTCF	chr12:10653707-10653947	Hela-S3	cervix:	n/a	n/a
40	CTCF	chr12:10653780-10653930	GM12872	blood:	n/a	n/a
41	CTCF	chr12:10653713-10653872	HepG2	liver:	n/a	n/a
42	CTCF	chr12:10653700-10653850	HA-sp	spinal cord:	n/a	n/a
43	CTCF	chr12:10653720-10653870	GM12865	blood:	n/a	n/a
44	CTCF	chr12:10653677-10653954	K562	blood:	n/a	n/a
45	CTCF	chr12:10653740-10653890	HPAF	blood vessel:	n/a	n/a
46	CTCF	chr12:10653680-10653830	HUVEC	blood vessel:	n/a	n/a
47	CTCF	chr12:10653780-10653930	GM12878	blood:	n/a	n/a
48	CTCF	chr12:10653744-10653913	LNCaP	prostate:	n/a	n/a
49	CTCF	chr12:10653760-10653910	AoAF	blood vessel:	n/a	n/a
50	CTCF	chr12:10651260-10651410	Caco-2	colon:	n/a	n/a

(count:429 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:10605936-10605986	HIPEpiC	eye:	n/a
2	chr12:10605936-10605986	U87	brain:	n/a
3	chr12:10605936-10605986	HIPEpiC	eye:	n/a
4	chr12:10605936-10605986	U87	brain:	n/a
5	chr12:10605936-10605986	ovcar-3	ovarian:	n/a
6	chr12:10607364-10607414	MCF-7	breast:	n/a
7	chr12:10658539-10658589	HL-60	blood:	n/a
8	chr12:10658425-10658475	AG09319	gingival:	n/a
9	chr12:10608067-10608117	HRPEpiC	eye:	n/a
10	chr12:10658425-10658475	NT2-D1	testis:	n/a
11	chr12:10658539-10658589	IMR90	lung:	fetal
12	chr12:10607364-10607414	CMK	blood:	n/a
13	chr12:10658539-10658589	PFSK-1	brain:	n/a
14	chr12:10658281-10658331	CMK	blood:	n/a
15	chr12:10608067-10608117	NT2-D1	testis:	n/a
16	chr12:10607364-10607414	GM12878	blood:	n/a
17	chr12:10658281-10658331	GM12878	blood:	n/a
18	chr12:10658281-10658331	BJ	skin:	n/a
19	chr12:10607364-10607414	NHBE	bronchial:	n/a
20	chr12:10607538-10607588	HepG2	liver:	n/a
21	chr12:10658425-10658475	RPTEC	kidney:	n/a
22	chr12:10607364-10607414	H1-hESC	embryonic stem cell:	embryo
23	chr12:10607538-10607588	SK-N-SH	brain:	n/a
24	chr12:10608067-10608117	AG04450	lung:	fetal
25	chr12:10658281-10658331	HNPCEpiC	eye:	n/a
26	chr12:10608067-10608117	ECC-1	luminal epithelium:	n/a
27	chr12:10607364-10607414	AG09309	skin:	n/a
28	chr12:10607538-10607588	Caco-2	colon:	n/a
29	chr12:10607364-10607414	BJ	skin:	n/a
30	chr12:10608067-10608117	GM19239	blood:	n/a
31	chr12:10607364-10607414	AG04449	skin:	fetal
32	chr12:10658539-10658589	NHBE	bronchial:	n/a
33	chr12:10605936-10605986	GM06990	blood:	n/a
34	chr12:10658425-10658475	T-47D	breast:	n/a
35	chr12:10658281-10658331	NT2-D1	testis:	n/a
36	chr12:10607538-10607588	GM06990	blood:	n/a
37	chr12:10658539-10658589	T-47D	breast:	n/a
38	chr12:10607538-10607588	HRPEpiC	eye:	n/a
39	chr12:10608067-10608117	AG04449	skin:	fetal
40	chr12:10658539-10658589	GM06990	blood:	n/a
41	chr12:10658281-10658331	HCT-116	colon:	n/a
42	chr12:10607364-10607414	Caco-2	colon:	n/a
43	chr12:10658425-10658475	A549	lung:	n/a
44	chr12:10607538-10607588	AG04449	skin:	fetal
45	chr12:10605936-10605986	CMK	blood:	n/a
46	chr12:10658281-10658331	HPAEpiC	pulmonary alveolar:	n/a
47	chr12:10607364-10607414	SK-N-SH	brain:	n/a
48	chr12:10658281-10658331	Hela-S3	cervix:	n/a
49	chr12:10658539-10658589	HCT-116	colon:	n/a
50	chr12:10658539-10658589	HIPEpiC	eye:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr12:10484099..10484956-chr12:10652861..10653779,2	MCF-7	breast:
2	chr12:10604438..10606172-chr12:10606795..10608691,2	K562	blood:
3	chr12:10693047..10695502-chr12:10698886..10701191,2	K562	blood:
4	chr12:10388252..10388816-chr12:10653557..10654233,2	MCF-7	breast:
5	chr12:10604438..10606172-chr12:10606795..10608691,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000180574	TF binding region
KLRC1	TF binding region
ENSG00000180574	CpG island
KLRC1	CpG island
ENSG00000134545	chromatin interactions

Extended variants
information (count: 1920 )
Associated
traits (count: 89 )

Variant overlapped rSNPs/rCNVs (count:1920 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1967432	chr12:10604945-10604946	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs3926123	chr12:10605014-10605015	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs186205144	chr12:10605017-10605018	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs530299839	chr12:10605024-10605025	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs377601205	chr12:10605025-10605026	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs572443429	chr12:10605081-10605082	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs138388320	chr12:10605098-10605099	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs2734438	chr12:10605114-10605115	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs574971041	chr12:10605139-10605140	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs190667355	chr12:10605208-10605209	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs563498192	chr12:10605252-10605253	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs532164000	chr12:10605260-10605261	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs370645870	chr12:10605292-10605293	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs552456903	chr12:10605384-10605385	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs559379917	chr12:10605385-10605386	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs550468454	chr12:10605429-10605430	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs7953443	chr12:10605434-10605435	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs547859398	chr12:10605514-10605515	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs183671850	chr12:10605528-10605529	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs536767897	chr12:10605554-10605555	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs186364899	chr12:10605555-10605556	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs2682472	chr12:10605571-10605572	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
23	rs538847063	chr12:10605598-10605599	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs371021989	chr12:10605600-10605601	Weak transcription Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs559247981	chr12:10605650-10605651	Weak transcription Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs548504262	chr12:10605651-10605652	Weak transcription Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs572630729	chr12:10605654-10605655	Weak transcription Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs148815969	chr12:10605710-10605711	Weak transcription Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs114439078	chr12:10605714-10605715	Weak transcription Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs12304307	chr12:10605715-10605716	Weak transcription Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs543940333	chr12:10605737-10605738	Weak transcription Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs373157153	chr12:10605820-10605821	Weak transcription Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs374670728	chr12:10605829-10605830	Weak transcription Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs191263231	chr12:10605841-10605842	Weak transcription Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs566169253	chr12:10605904-10605905	Weak transcription Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs74062026	chr12:10605936-10605937	Weak transcription Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs182631267	chr12:10605937-10605938	Weak transcription Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs528389160	chr12:10606014-10606015	Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs548049932	chr12:10606040-10606041	Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs2734437	chr12:10606130-10606131	Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs147016885	chr12:10606135-10606136	Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs550300909	chr12:10606152-10606153	Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs35500295	chr12:10606164-10606165	Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs3809216	chr12:10606175-10606176	Enhancers Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs539250625	chr12:10606208-10606209	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs536907463	chr12:10606238-10606239	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs74923722	chr12:10606289-10606290	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs11053805	chr12:10606337-10606338	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs148419751	chr12:10606394-10606395	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs552480542	chr12:10606439-10606440	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:89)

Disease	PMID	Source
Acute lymphoblastic leukemia	17690704	CNVD
Medulloblastoma	16968546	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Hepatocellular carcinoma	16750200	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Breast cancer	22032731	CNVD
Cancer	21183584	CNVD
Myxofibrosarcoma	16751306	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Prostate cancer	21965145	CNVD
Acute myeloid leukemia	16864856	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Disorders of sex development	21048976	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Prostate cancer	19156837	CNVD
Emphysema	19352772	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Malignant germ cell tumour	17285132	CNVD
Melanoma	18172304	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Wilms tumour	21544195	CNVD
Squamous cell cancer	21044232	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Endometrial cancer	22040021	CNVD
Colorectal cancer	20709793	CNVD
Breast cancer	21264507	CNVD
Cancer	16751803	CNVD
Testicular cancer	18059402	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Seminomas	18059402	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
Testicular germ cell tumor	18059402	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Ewing''s sarcoma	17952124	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	21858162	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21785460	CNVD
Myelodysplastic syndrome	21251322	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21611746	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Myelofibrosis	22110671	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Squamous cell cancer	19607727	CNVD
Prostate cancer	16573809	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Glioblastoma multiforme	22286061	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Acute myeloid leukemia	17268525	CNVD
Acute monocytic leukemia	16498392	CNVD
Prostate cancer	16461572	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17133270	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:118 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:10600800-10606000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr12:10604000-10606200	Active TSS	Primary Natural Killer cells fromperipheralblood	blood
3	chr12:10605600-10606000	Enhancers	HMEC	breast
4	chr12:10605600-10606200	Enhancers	Rectal Mucosa Donor 31	rectum
5	chr12:10606000-10606200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr12:10606200-10606800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
7	chr12:10606200-10607000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr12:10606800-10607200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
9	chr12:10607000-10607200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
10	chr12:10607000-10607400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr12:10607000-10607600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr12:10607000-10607600	Enhancers	Muscle Satellite Cultured Cells	--
13	chr12:10607000-10607800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
14	chr12:10607200-10608000	ZNF genes & repeats	Primary Natural Killer cells fromperipheralblood	blood
15	chr12:10607400-10610400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr12:10607600-10625400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
17	chr12:10609400-10609600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
18	chr12:10609600-10610000	Enhancers	HUES48 Cell Line	embryonic stem cell
19	chr12:10609600-10610200	Enhancers	iPS-20b Cell Line	embryonic stem cell
20	chr12:10609600-10611000	Enhancers	ES-I3 Cell Line	embryonic stem cell
21	chr12:10609600-10611000	Enhancers	iPS-15b Cell Line	embryonic stem cell
22	chr12:10610000-10610400	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
23	chr12:10610000-10610800	Enhancers	HUES64 Cell Line	embryonic stem cell
24	chr12:10610000-10610800	Enhancers	iPS-18 Cell Line	embryonic stem cell
25	chr12:10610000-10611000	Enhancers	HUES6 Cell Line	embryonic stem cell
26	chr12:10610200-10610400	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
27	chr12:10610200-10610800	Enhancers	H9 Cell Line	embryonic stem cell
28	chr12:10610400-10610600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
29	chr12:10610400-10610800	Enhancers	HUES48 Cell Line	embryonic stem cell
30	chr12:10610400-10610800	Active TSS	iPS-20b Cell Line	embryonic stem cell
31	chr12:10621200-10622400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
32	chr12:10631200-10631600	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
33	chr12:10631400-10631600	ZNF genes & repeats	Thymus	Thymus
34	chr12:10631600-10631800	Enhancers	Thymus	Thymus
35	chr12:10633000-10635600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
36	chr12:10633800-10635000	Enhancers	Primary T cells from cord blood	blood
37	chr12:10633800-10635400	Enhancers	Primary T cells fromperipheralblood	blood
38	chr12:10633800-10635400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
39	chr12:10634000-10635400	Enhancers	Primary B cells from peripheral blood	blood
40	chr12:10634000-10635400	Enhancers	Primary T killer memory cells from peripheral blood	blood
41	chr12:10634800-10635400	Enhancers	Primary T helper naive cells from peripheral blood	blood
42	chr12:10646400-10646600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
43	chr12:10646400-10646800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
44	chr12:10649800-10651600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
45	chr12:10650200-10650400	Enhancers	Primary T killer memory cells from peripheral blood	blood
46	chr12:10650200-10651800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
47	chr12:10650400-10650800	Bivalent Enhancer	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
48	chr12:10650400-10651000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
49	chr12:10650600-10652000	Enhancers	Primary T helper naive cells from peripheral blood	blood
50	chr12:10651000-10651800	Enhancers	Primary T killer memory cells from peripheral blood	blood

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