Variant report

Variant	nsv557477
Chromosome Location	chr12:10601690-10698255
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:363)
CpG islands
(count:430)
Chromatin interactive
region (count:5)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:363 , 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	chr12:10693152-10694036	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	chr12:10695883-10696624	GM12878	blood:	n/a	n/a
6	BATF	chr12:10641906-10642182	GM12878	blood:	n/a	chr12:10642014-10642025
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	chr12:10693300-10693868	GM12878	blood:	n/a	chr12:10693650-10693661
10	BATF	chr12:10693317-10693939	GM12878	blood:	n/a	chr12:10693650-10693661
11	BATF	chr12:10696061-10696446	GM12878	blood:	n/a	n/a
12	BCL11A	chr12:10693354-10693625	GM12878	blood:	n/a	n/a
13	BCL11A	chr12:10696199-10696390	GM12878	blood:	n/a	n/a
14	BCL11A	chr12:10671811-10671985	GM12878	blood:	n/a	n/a
15	BCL11A	chr12:10696076-10696426	GM12878	blood:	n/a	n/a
16	BCL11A	chr12:10693310-10693858	GM12878	blood:	n/a	n/a
17	BCL3	chr12:10695995-10696628	GM12878	blood:	n/a	n/a
18	BCL3	chr12:10693360-10693849	GM12878	blood:	n/a	n/a
19	BCL3	chr12:10693210-10693959	GM12878	blood:	n/a	n/a
20	BCL3	chr12:10696031-10696586	GM12878	blood:	n/a	n/a
21	BCLAF1	chr12:10693217-10694044	GM12878	blood:	n/a	n/a
22	BCLAF1	chr12:10696071-10696445	GM12878	blood:	n/a	n/a
23	BCLAF1	chr12:10693241-10693808	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	chr12:10605885-10606198	A549	lung:	n/a	chr12:10606038-10606049
28	CEBPB	chr12:10605854-10606222	Hela-S3	cervix:	n/a	chr12:10606038-10606049
29	CEBPB	chr12:10605878-10606169	IMR90	lung:	n/a	chr12:10606038-10606049
30	CEBPB	chr12:10675319-10675536	HepG2	liver:	n/a	chr12:10675436-10675447
31	CEBPB	chr12:10605864-10606214	HepG2	liver:	n/a	chr12:10606038-10606049
32	CEBPB	chr12:10675342-10675509	A549	lung:	n/a	chr12:10675436-10675447
33	CEBPB	chr12:10693180-10693997	GM12878	blood:	n/a	n/a
34	CEBPB	chr12:10695688-10696520	GM12878	blood:	n/a	n/a
35	CREB1	chr12:10693203-10694090	GM12878	blood:	n/a	n/a
36	CREB1	chr12:10674190-10674624	GM12878	blood:	n/a	n/a
37	CREB1	chr12:10693316-10693819	GM12878	blood:	n/a	n/a
38	CTCF	chr12:10653707-10653947	Hela-S3	cervix:	n/a	n/a
39	CTCF	chr12:10653634-10653989	GM12878	blood:	n/a	n/a
40	CTCF	chr12:10653680-10653830	Caco-2	colon:	n/a	n/a
41	CTCF	chr12:10653734-10653915	HUVEC	blood vessel:	n/a	n/a
42	CTCF	chr12:10653660-10653810	HBMEC	blood vessel:	n/a	n/a
43	CTCF	chr12:10653740-10653890	MCF-7	breast:	n/a	n/a
44	CTCF	chr12:10653695-10653910	A549	lung:	n/a	n/a
45	CTCF	chr12:10653740-10653890	AG09319	gingival:	n/a	n/a
46	CTCF	chr12:10653800-10653950	NHDF-neo	bronchial:	n/a	n/a
47	CTCF	chr12:10621340-10621490	HA-sp	spinal cord:	n/a	n/a
48	CTCF	chr12:10653731-10653926	K562	blood:	n/a	n/a
49	CTCF	chr12:10653740-10653890	SAEC	small airway:	n/a	n/a
50	CTCF	chr12:10621320-10621470	HepG2	liver:	n/a	n/a

(count:430 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:10607364-10607414	MCF10A-Er-Src	breast:	n/a
2	chr12:10658425-10658475	AoSMC	blood vessel:	n/a
3	chr12:10607538-10607588	HNPCEpiC	eye:	n/a
4	chr12:10607364-10607414	MCF10A-Er-Src	breast:	n/a
5	chr12:10658425-10658475	AoSMC	blood vessel:	n/a
6	chr12:10607538-10607588	HNPCEpiC	eye:	n/a
7	chr12:10608067-10608117	Jurkat	blood:	n/a
8	chr12:10607364-10607414	ovcar-3	ovarian:	n/a
9	chr12:10658539-10658589	NHBE	bronchial:	n/a
10	chr12:10658281-10658331	AG04449	skin:	fetal
11	chr12:10658425-10658475	HRE	kidney:	n/a
12	chr12:10658425-10658475	HRCEpiC	kidney:	n/a
13	chr12:10658281-10658331	SKMC	muscle:	n/a
14	chr12:10658281-10658331	HEEpiC	esophagus:	n/a
15	chr12:10607364-10607414	SKMC	muscle:	n/a
16	chr12:10658281-10658331	HCM	heart:	n/a
17	chr12:10607364-10607414	GM19239	blood:	n/a
18	chr12:10605936-10605986	GM12892	blood:	n/a
19	chr12:10607538-10607588	GM12891	blood:	n/a
20	chr12:10607364-10607414	GM12878	blood:	n/a
21	chr12:10608067-10608117	AG09319	gingival:	n/a
22	chr12:10658539-10658589	ProgFib	skin:	n/a
23	chr12:10607538-10607588	GM12878	blood:	n/a
24	chr12:10605936-10605986	HepG2	liver:	n/a
25	chr12:10608067-10608117	AG04450	lung:	fetal
26	chr12:10605936-10605986	HIPEpiC	eye:	n/a
27	chr12:10605936-10605986	IMR90	lung:	fetal
28	chr12:10605936-10605986	RPTEC	kidney:	n/a
29	chr12:10607364-10607414	ECC-1	luminal epithelium:	n/a
30	chr12:10658281-10658331	BJ	skin:	n/a
31	chr12:10605936-10605986	Hepatocyte	liver:	n/a
32	chr12:10605936-10605986	Hela-S3	cervix:	n/a
33	chr12:10608067-10608117	K562	blood:	n/a
34	chr12:10605936-10605986	HL-60	blood:	n/a
35	chr12:10658281-10658331	PANC-1	pancreas:	n/a
36	chr12:10607538-10607588	BE2_C	brain:	n/a
37	chr12:10658539-10658589	LNCaP	prostate:	n/a
38	chr12:10658539-10658589	SKMC	muscle:	n/a
39	chr12:10658425-10658475	HUVEC	blood vessel:	n/a
40	chr12:10605936-10605986	PFSK-1	brain:	n/a
41	chr12:10605936-10605986	Jurkat	blood:	n/a
42	chr12:10607364-10607414	LNCaP	prostate:	n/a
43	chr12:10607364-10607414	ProgFib	skin:	n/a
44	chr12:10658425-10658475	K562	blood:	n/a
45	chr12:10605936-10605986	ProgFib	skin:	n/a
46	chr12:10607538-10607588	PFSK-1	brain:	n/a
47	chr12:10607538-10607588	Jurkat	blood:	n/a
48	chr12:10607364-10607414	K562	blood:	n/a
49	chr12:10608067-10608117	IMR90	lung:	fetal
50	chr12:10607538-10607588	SK-N-SH	brain:	n/a

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

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

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-EIF2S3L.1-6	chr12:10601202-10602083	l_610_chr12:10597245-10602083_whiteBloodCell

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: 2077 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:2077 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7301582	chr12:10601690-10601691	Weak transcription Strong transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs71448846	chr12:10601710-10601711	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
3	rs187283639	chr12:10601746-10601747	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
4	rs567607129	chr12:10601758-10601759	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
5	rs531176256	chr12:10601765-10601766	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
6	rs71451714	chr12:10601769-10601770	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
7	rs71448847	chr12:10601781-10601782	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
8	rs141355168	chr12:10601782-10601783	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
9	rs147421369	chr12:10601792-10601793	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
10	rs201161302	chr12:10601801-10601802	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
11	rs71451715	chr12:10601812-10601813	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
12	rs71451716	chr12:10601818-10601819	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
13	rs374638306	chr12:10601827-10601828	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
14	rs547241730	chr12:10601847-10601848	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
15	rs368241749	chr12:10601852-10601853	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
16	rs139780190	chr12:10601904-10601905	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
17	rs372070161	chr12:10601919-10601920	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
18	rs142953321	chr12:10601950-10601951	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
19	rs376062790	chr12:10601985-10601986	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
20	rs368167526	chr12:10601994-10601995	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
21	rs200705945	chr12:10602012-10602013	Weak transcription Transcr. at gene 5' and 3'	lncRNA	n/a	Overlapped CNVs	n/a
22	rs71300186	chr12:10602058-10602059	Weak transcription Transcr. at gene 5' and 3'	lncRNA	n/a	Overlapped CNVs	n/a
23	rs566757137	chr12:10602075-10602076	Weak transcription Transcr. at gene 5' and 3'	lncRNA	n/a	Overlapped CNVs	n/a
24	rs2734440	chr12:10602077-10602078	Weak transcription Transcr. at gene 5' and 3'	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
25	rs139685995	chr12:10602105-10602106	Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
26	rs555483664	chr12:10602140-10602141	Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
27	rs71451718	chr12:10602156-10602157	Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
28	rs71451719	chr12:10602160-10602161	Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
29	rs71451720	chr12:10602168-10602169	Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
30	rs71451721	chr12:10602174-10602175	Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
31	rs71451722	chr12:10602177-10602178	Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
32	rs569010543	chr12:10602199-10602200	Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
33	rs549882997	chr12:10602208-10602209	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs71452585	chr12:10602211-10602212	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs71451723	chr12:10602223-10602224	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs71451783	chr12:10602231-10602232	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs537678584	chr12:10602235-10602236	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs557514825	chr12:10602237-10602238	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs71451784	chr12:10602238-10602239	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs71451785	chr12:10602245-10602246	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs577384046	chr12:10602270-10602271	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs143274044	chr12:10602273-10602274	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs540181504	chr12:10602281-10602282	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs553992347	chr12:10602282-10602283	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs61917722	chr12:10602301-10602302	Weak transcription Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs542605086	chr12:10602343-10602344	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs562600027	chr12:10602357-10602358	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs147281263	chr12:10602479-10602480	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs139766707	chr12:10602509-10602510	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs113215493	chr12:10602518-10602519	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:90)

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
early-passage human iPS cells	21368824	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:124 , 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	chr12:10601400-10602000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
3	chr12:10602000-10602200	Transcr. at gene 5' and 3'	Primary Natural Killer cells fromperipheralblood	blood
4	chr12:10602200-10602800	Active TSS	Primary Natural Killer cells fromperipheralblood	blood
5	chr12:10602800-10604000	Transcr. at gene 5' and 3'	Primary Natural Killer cells fromperipheralblood	blood
6	chr12:10603200-10603600	Active TSS	Primary mononuclear cells fromperipheralblood	Blood
7	chr12:10603400-10603800	Active TSS	Primary T cells fromperipheralblood	blood
8	chr12:10604000-10606200	Active TSS	Primary Natural Killer cells fromperipheralblood	blood
9	chr12:10605600-10606000	Enhancers	HMEC	breast
10	chr12:10605600-10606200	Enhancers	Rectal Mucosa Donor 31	rectum
11	chr12:10606000-10606200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr12:10606200-10606800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
13	chr12:10606200-10607000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr12:10606800-10607200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
15	chr12:10607000-10607200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr12:10607000-10607400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr12:10607000-10607600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
18	chr12:10607000-10607600	Enhancers	Muscle Satellite Cultured Cells	--
19	chr12:10607000-10607800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
20	chr12:10607200-10608000	ZNF genes & repeats	Primary Natural Killer cells fromperipheralblood	blood
21	chr12:10607400-10610400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
22	chr12:10607600-10625400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
23	chr12:10609400-10609600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
24	chr12:10609600-10610000	Enhancers	HUES48 Cell Line	embryonic stem cell
25	chr12:10609600-10610200	Enhancers	iPS-20b Cell Line	embryonic stem cell
26	chr12:10609600-10611000	Enhancers	ES-I3 Cell Line	embryonic stem cell
27	chr12:10609600-10611000	Enhancers	iPS-15b Cell Line	embryonic stem cell
28	chr12:10610000-10610400	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
29	chr12:10610000-10610800	Enhancers	HUES64 Cell Line	embryonic stem cell
30	chr12:10610000-10610800	Enhancers	iPS-18 Cell Line	embryonic stem cell
31	chr12:10610000-10611000	Enhancers	HUES6 Cell Line	embryonic stem cell
32	chr12:10610200-10610400	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
33	chr12:10610200-10610800	Enhancers	H9 Cell Line	embryonic stem cell
34	chr12:10610400-10610600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
35	chr12:10610400-10610800	Enhancers	HUES48 Cell Line	embryonic stem cell
36	chr12:10610400-10610800	Active TSS	iPS-20b Cell Line	embryonic stem cell
37	chr12:10621200-10622400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
38	chr12:10631200-10631600	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
39	chr12:10631400-10631600	ZNF genes & repeats	Thymus	Thymus
40	chr12:10631600-10631800	Enhancers	Thymus	Thymus
41	chr12:10633000-10635600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
42	chr12:10633800-10635000	Enhancers	Primary T cells from cord blood	blood
43	chr12:10633800-10635400	Enhancers	Primary T cells fromperipheralblood	blood
44	chr12:10633800-10635400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
45	chr12:10634000-10635400	Enhancers	Primary B cells from peripheral blood	blood
46	chr12:10634000-10635400	Enhancers	Primary T killer memory cells from peripheral blood	blood
47	chr12:10634800-10635400	Enhancers	Primary T helper naive cells from peripheral blood	blood
48	chr12:10646400-10646600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
49	chr12:10646400-10646800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
50	chr12:10649800-10651600	Enhancers	Primary T killer naive cells fromperipheralblood	blood

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