Variant report

Variant	nsv997538
Chromosome Location	chr2:12216408-12242734
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:251)
CpG islands
(count:122)
Chromatin interactive
region (count:15)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:251 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:12224320-12224487	K562	blood:	n/a	n/a
2	ATF1	chr2:12224211-12224502	K562	blood:	n/a	n/a
3	ATF2	chr2:12216889-12217266	GM12878	blood:	n/a	n/a
4	BATF	chr2:12216963-12217290	GM12878	blood:	n/a	n/a
5	BCL11A	chr2:12223232-12223426	H1-hESC	embryonic stem cell:	n/a	n/a
6	BCL3	chr2:12237953-12238250	GM12878	blood:	n/a	n/a
7	BCL3	chr2:12228185-12228478	GM12878	blood:	n/a	n/a
8	BHLHE40	chr2:12224257-12224263	K562	blood:	n/a	n/a
9	BHLHE40	chr2:12216985-12217153	K562	blood:	n/a	n/a
10	CBX3	chr2:12237955-12238380	K562	blood:	n/a	n/a
11	CCNT2	chr2:12228800-12228880	K562	blood:	n/a	n/a
12	CEBPB	chr2:12224881-12225055	HepG2	liver:	n/a	chr2:12224988-12224999
13	CEBPB	chr2:12236525-12236793	H1-hESC	embryonic stem cell:	n/a	n/a
14	CEBPB	chr2:12227729-12228709	A549	lung:	n/a	n/a
15	CEBPB	chr2:12228988-12229232	K562	blood:	n/a	chr2:12229112-12229123 chr2:12229114-12229125 chr2:12229112-12229125
16	CEBPB	chr2:12228192-12228546	IMR90	lung:	n/a	n/a
17	CEBPB	chr2:12230894-12231029	A549	lung:	n/a	n/a
18	CEBPB	chr2:12228321-12228463	K562	blood:	n/a	n/a
19	CEBPB	chr2:12224859-12225113	K562	blood:	n/a	chr2:12224988-12224999
20	CEBPB	chr2:12228182-12228541	Hela-S3	cervix:	n/a	n/a
21	CEBPB	chr2:12224141-12224512	K562	blood:	n/a	n/a
22	CEBPB	chr2:12228997-12229197	HepG2	liver:	n/a	chr2:12229112-12229123 chr2:12229114-12229125 chr2:12229112-12229125
23	CEBPB	chr2:12228193-12228571	A549	lung:	n/a	n/a
24	CEBPB	chr2:12227889-12227944	H1-hESC	embryonic stem cell:	n/a	n/a
25	CEBPB	chr2:12218182-12218312	K562	blood:	n/a	chr2:12218207-12218220 chr2:12218207-12218218
26	CEBPB	chr2:12228102-12228594	MCF-7	breast:	n/a	n/a
27	CEBPB	chr2:12228209-12228545	A549	lung:	n/a	n/a
28	CEBPB	chr2:12224173-12224456	K562	blood:	n/a	n/a
29	CEBPB	chr2:12228105-12228643	MCF-7	breast:	n/a	n/a
30	CEBPB	chr2:12224269-12224448	H1-hESC	embryonic stem cell:	n/a	n/a
31	CEBPB	chr2:12224121-12224445	K562	blood:	n/a	n/a
32	CTBP2	chr2:12223146-12224127	H1-hESC	embryonic stem cell:	n/a	n/a
33	CTCF	chr2:12238065-12238280	K562	blood:	n/a	n/a
34	CTCF	chr2:12228160-12228310	RPTEC	kidney:	n/a	n/a
35	CTCF	chr2:12238090-12238336	K562	blood:	n/a	n/a
36	CTCF	chr2:12238019-12238369	K562	blood:	n/a	n/a
37	CTCF	chr2:12238134-12238248	HepG2	liver:	n/a	n/a
38	CTCF	chr2:12238000-12238150	RPTEC	kidney:	n/a	n/a
39	CTCF	chr2:12238131-12238194	MCF-7	breast:	n/a	n/a
40	CTCF	chr2:12231540-12231690	NHDF-neo	bronchial:	n/a	n/a
41	CTCF	chr2:12238100-12238250	K562	blood:	n/a	n/a
42	CUX1	chr2:12230692-12230700	K562	blood:	n/a	n/a
43	E2F4	chr2:12228200-12228518	MCF10A-Er-Src	breast:	n/a	n/a
44	E2F6	chr2:12238070-12238349	K562	blood:	n/a	n/a
45	E2F6	chr2:12221676-12222065	H1-hESC	embryonic stem cell:	n/a	n/a
46	E2F6	chr2:12238044-12238203	K562	blood:	n/a	n/a
47	E2F6	chr2:12223348-12223867	H1-hESC	embryonic stem cell:	n/a	n/a
48	EBF1	chr2:12216923-12217136	GM12878	blood:	n/a	n/a
49	ELF1	chr2:12224190-12224517	K562	blood:	n/a	chr2:12224318-12224331
50	EP300	chr2:12223097-12223601	H1-hESC	embryonic stem cell:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:12223636-12223686	AoSMC	blood vessel:	n/a
2	chr2:12237012-12237062	AoSMC	blood vessel:	n/a
3	chr2:12237012-12237062	MCF-7	breast:	n/a
4	chr2:12237012-12237062	ECC-1	luminal epithelium:	n/a
5	chr2:12237012-12237062	HAEpiC	amniotic membrane:	n/a
6	chr2:12223636-12223686	HRCEpiC	kidney:	n/a
7	chr2:12223636-12223686	HUVEC	blood vessel:	n/a
8	chr2:12223636-12223686	H1-hESC	embryonic stem cell:	embryo
9	chr2:12223636-12223686	SKMC	muscle:	n/a
10	chr2:12237012-12237062	AG04450	lung:	fetal
11	chr2:12223636-12223686	AG04449	skin:	fetal
12	chr2:12237012-12237062	HNPCEpiC	eye:	n/a
13	chr2:12237012-12237062	A549	lung:	n/a
14	chr2:12223636-12223686	Hela-S3	cervix:	n/a
15	chr2:12223636-12223686	AG09309	skin:	n/a
16	chr2:12237012-12237062	NHDF-neo	bronchial:	n/a
17	chr2:12237012-12237062	CMK	blood:	n/a
18	chr2:12223636-12223686	HEK293	kidney:	embryo
19	chr2:12237012-12237062	Hepatocyte	liver:	n/a
20	chr2:12237012-12237062	AG09309	skin:	n/a
21	chr2:12237012-12237062	MCF10A-Er-Src	breast:	n/a
22	chr2:12223636-12223686	MCF-7	breast:	n/a
23	chr2:12223636-12223686	BE2_C	brain:	n/a
24	chr2:12237012-12237062	GM19239	blood:	n/a
25	chr2:12237012-12237062	HRE	kidney:	n/a
26	chr2:12223636-12223686	BJ	skin:	n/a
27	chr2:12237012-12237062	Caco-2	colon:	n/a
28	chr2:12223636-12223686	AG04450	lung:	fetal
29	chr2:12223636-12223686	NT2-D1	testis:	n/a
30	chr2:12237012-12237062	GM12878	blood:	n/a
31	chr2:12223636-12223686	HMEC	breast:	n/a
32	chr2:12223636-12223686	SK-N-SH	brain:	n/a
33	chr2:12223636-12223686	GM19239	blood:	n/a
34	chr2:12223636-12223686	ProgFib	skin:	n/a
35	chr2:12223636-12223686	GM12878	blood:	n/a
36	chr2:12223636-12223686	A549	lung:	n/a
37	chr2:12223636-12223686	SK-N-MC	brain:	n/a
38	chr2:12237012-12237062	HPAEpiC	pulmonary alveolar:	n/a
39	chr2:12223636-12223686	HPAEpiC	pulmonary alveolar:	n/a
40	chr2:12237012-12237062	ProgFib	skin:	n/a
41	chr2:12223636-12223686	PANC-1	pancreas:	n/a
42	chr2:12223636-12223686	AG10803	skin:	n/a
43	chr2:12223636-12223686	ECC-1	luminal epithelium:	n/a
44	chr2:12237012-12237062	HUVEC	blood vessel:	n/a
45	chr2:12223636-12223686	HCT-116	colon:	n/a
46	chr2:12237012-12237062	NT2-D1	testis:	n/a
47	chr2:12237012-12237062	NHBE	bronchial:	n/a
48	chr2:12223636-12223686	MCF10A-Er-Src	breast:	n/a
49	chr2:12223636-12223686	U87	brain:	n/a
50	chr2:12237012-12237062	SKMC	muscle:	n/a

(count:15 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:12226565..12229995-chr2:12235703..12237819,3	K562	blood:
2	chr2:12228495..12230173-chr2:12235680..12237558,2	K562	blood:
3	chr2:12233977..12235737-chr2:12241751..12243264,2	K562	blood:
4	chr2:12233977..12235737-chr2:12241751..12243264,2	K562	blood:
5	chr2:12225032..12227788-chr2:12236883..12238625,2	K562	blood:
6	chr2:12222240..12225810-chr2:12227711..12231664,3	K562	blood:
7	chr2:12219592..12223181-chr2:12244088..12246187,3	K562	blood:
8	chr2:12226565..12229995-chr2:12235703..12237819,3	K562	blood:
9	chr2:12222114..12225189-chr2:12227458..12230399,3	K562	blood:
10	chr2:12194778..12196811-chr2:12221641..12223390,2	K562	blood:
11	chr2:12222114..12225189-chr2:12227458..12230399,3	K562	blood:
12	chr2:12225032..12227788-chr2:12236883..12238625,2	K562	blood:
13	chr2:12228495..12230173-chr2:12235680..12237558,2	K562	blood:
14	chr2:12222240..12225810-chr2:12227711..12231664,3	K562	blood:
15	chr2:12240589..12242524-chr2:12244995..12247436,2	K562	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LPIN1-1	chr2:12223575-12223744	ENSG00000224184
2	lnc-LPIN1-1	chr2:12223575-12223743	NR_110198
3	lnc-GREB1-10	chr2:12224315-12224432	NONHSAT069210
4	lnc-GREB1-10	chr2:12224315-12224432	NONHSAT069196

No data

Variant related genes	Relation type
ENSG00000224184	TF binding region
ENSG00000224184	CpG island
ENSG00000224184	chromatin interactions

Extended variants
information (count: 1080 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:1080 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs3845756	chr2:12216408-12216409	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs575627743	chr2:12216413-12216414	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs543152013	chr2:12216429-12216430	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs561428947	chr2:12216460-12216461	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs117921060	chr2:12216467-12216468	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs72610740	chr2:12216530-12216531	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs559814164	chr2:12216560-12216561	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs533638541	chr2:12216566-12216567	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs545078892	chr2:12216646-12216647	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs183905557	chr2:12216647-12216648	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs112429349	chr2:12216651-12216652	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs187865085	chr2:12216665-12216666	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs538348602	chr2:12216681-12216682	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs541990211	chr2:12216697-12216698	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs554626993	chr2:12216784-12216785	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs368255326	chr2:12216921-12216922	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs144072110	chr2:12216938-12216939	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs529099127	chr2:12216945-12216946	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs576473022	chr2:12216954-12216955	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs547528818	chr2:12216964-12216965	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs565838850	chr2:12217009-12217010	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs192496393	chr2:12217017-12217018	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs79580022	chr2:12217032-12217033	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs373639425	chr2:12217065-12217066	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs372504017	chr2:12217070-12217071	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs536625970	chr2:12217092-12217093	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs555061663	chr2:12217114-12217115	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs573649527	chr2:12217140-12217141	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs541276899	chr2:12217153-12217154	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs553486736	chr2:12217154-12217155	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs561751569	chr2:12217158-12217159	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs146940089	chr2:12217200-12217201	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs545726310	chr2:12217219-12217220	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs568457806	chr2:12217232-12217233	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs563957735	chr2:12217262-12217263	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs375456256	chr2:12217263-12217264	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs183209953	chr2:12217293-12217294	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs187280247	chr2:12217299-12217300	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs528539010	chr2:12217316-12217317	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs546775358	chr2:12217347-12217348	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs149496516	chr2:12217363-12217364	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs532965005	chr2:12217368-12217369	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs143919645	chr2:12217375-12217376	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs191856371	chr2:12217385-12217386	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs561961749	chr2:12217422-12217423	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs554905092	chr2:12217470-12217471	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs368629060	chr2:12217499-12217500	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs184405042	chr2:12217524-12217525	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs189080699	chr2:12217551-12217552	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs552784681	chr2:12217581-12217582	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:64)

Disease	PMID	Source
Glioblastoma multiforme	21080181	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Cancer	20164920	CNVD
Neuroblastoma	21508638	CNVD
Breast cancer	17603634	CNVD
Cancer	16751803	CNVD
Neuroblastoma	16790693	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	17393978	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17387387	CNVD
Neuroblastoma	17533364	CNVD
Neuroblastoma	18923191	CNVD
Endometrial cancer	22040021	CNVD
Adrenal tumor	17535989	CNVD
Breast cancer	21264507	CNVD
Basal cell lymphoma	17053054	CNVD
Medulloblastoma	17522785	CNVD
Cancer	23418310	CNVD
Ewing''s sarcoma	21437220	CNVD
Ependymoma	16718352	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
lymphocytic leukemia	21291569	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Bladder cancer	21909424	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	20505157	CNVD
Autism	17483303	CNVD
Breast cancer	21804112	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21785460	CNVD
Medulloblastoma	20607354	CNVD
Acute myeloid leukemia	20729466	CNVD
Medulloblastoma	19270706	CNVD
Prostate cancer	19258504	CNVD
Neuroblastoma	19638189	CNVD
Neuroblastoma	19435921	CNVD
Neuroblastoma	18574593	CNVD
Acute myeloid leukemia	18000384	CNVD
Medulloblastoma	16968546	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:285 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:12213600-12218600	Enhancers	Cortex derived primary cultured neurospheres	brain
2	chr2:12214800-12216800	Weak transcription	Brain Inferior Temporal Lobe	brain
3	chr2:12214800-12217400	Enhancers	GM12878-XiMat	blood
4	chr2:12215200-12216600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
5	chr2:12215400-12224200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
6	chr2:12215600-12216600	Weak transcription	K562	blood
7	chr2:12216200-12216600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr2:12216400-12216800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
9	chr2:12216400-12217000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr2:12216400-12217200	Enhancers	Primary B cells from cord blood	blood
11	chr2:12216400-12217200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
12	chr2:12216400-12217800	Enhancers	Primary B cells from peripheral blood	blood
13	chr2:12216400-12218400	Enhancers	Brain Germinal Matrix	brain
14	chr2:12216600-12216800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr2:12216600-12217200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
16	chr2:12216600-12217600	Enhancers	K562	blood
17	chr2:12216800-12217400	Enhancers	Fetal Lung	lung
18	chr2:12216800-12217400	Enhancers	HSMMtube	muscle
19	chr2:12216800-12217800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
20	chr2:12216800-12218400	Enhancers	Fetal Brain Female	brain
21	chr2:12216800-12218800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr2:12217000-12217200	Enhancers	Brain Inferior Temporal Lobe	brain
23	chr2:12217000-12217200	Enhancers	Fetal Stomach	stomach
24	chr2:12217200-12220400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
25	chr2:12217400-12223200	Weak transcription	Fetal Lung	lung
26	chr2:12217400-12249800	Weak transcription	GM12878-XiMat	blood
27	chr2:12217600-12219400	Weak transcription	K562	blood
28	chr2:12217800-12218200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
29	chr2:12217800-12223000	Weak transcription	Primary B cells from peripheral blood	blood
30	chr2:12218200-12218400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
31	chr2:12218400-12222000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
32	chr2:12218600-12221600	Weak transcription	Cortex derived primary cultured neurospheres	brain
33	chr2:12218800-12220000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr2:12219000-12219200	Enhancers	iPS-15b Cell Line	embryonic stem cell
35	chr2:12219400-12220000	Enhancers	K562	blood
36	chr2:12219600-12219800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
37	chr2:12219600-12223600	Enhancers	ES-I3 Cell Line	embryonic stem cell
38	chr2:12219800-12222000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
39	chr2:12220000-12223200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr2:12220000-12223200	Weak transcription	K562	blood
41	chr2:12220400-12220800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
42	chr2:12220600-12220800	Enhancers	Spleen	Spleen
43	chr2:12220600-12222400	Enhancers	iPS-18 Cell Line	embryonic stem cell
44	chr2:12220600-12223600	Enhancers	Primary T cells from cord blood	blood
45	chr2:12220800-12221800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
46	chr2:12221000-12224800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
47	chr2:12221000-12234200	Weak transcription	Spleen	Spleen
48	chr2:12221200-12222400	Enhancers	Primary T helper naive cells from peripheral blood	blood
49	chr2:12221200-12222600	Enhancers	Primary T helper cells fromperipheralblood	blood
50	chr2:12221200-12223400	Enhancers	Primary T cells fromperipheralblood	blood

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