Variant report

Variant	esv3499585
Chromosome Location	chr12:2028791-2033089
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:59)
CpG islands
(count:671)
Chromatin interactive
region (count:6)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:59 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BHLHE40	chr12:2031760-2031813	K562	blood:	n/a	n/a
2	CTCF	chr12:2031754-2031883	HepG2	liver:	n/a	chr12:2031831-2031849 chr12:2031832-2031848
3	CTCF	chr12:2031257-2031393	H1-hESC	embryonic stem cell:	n/a	n/a
4	CTCF	chr12:2031301-2031343	GM10266	blood:	n/a	n/a
5	CTCF	chr12:2031240-2031390	HA-sp	spinal cord:	n/a	n/a
6	CTCF	chr12:2031264-2031372	IMR90	lung:	n/a	n/a
7	CTCF	chr12:2031280-2031430	HUVEC	blood vessel:	n/a	n/a
8	CTCF	chr12:2030176-2030363	K562	blood:	n/a	chr12:2030323-2030336
9	CTCF	chr12:2031222-2031411	GM19238	blood:	n/a	n/a
10	CTCF	chr12:2031800-2031950	GM12873	blood:	n/a	chr12:2031831-2031849 chr12:2031832-2031848
11	CTCF	chr12:2031200-2031350	GM12868	blood:	n/a	n/a
12	CTCF	chr12:2031213-2031459	GM19239	blood:	n/a	n/a
13	CTCF	chr12:2030270-2030390	Spleen_OC	spleen:	n/a	chr12:2030323-2030336
14	CTCF	chr12:2030220-2030370	GM12873	blood:	n/a	chr12:2030323-2030336
15	CTCF	chr12:2031265-2031393	Fibrobl	skin:	n/a	n/a
16	CTCF	chr12:2031239-2031413	H1-hESC	embryonic stem cell:	n/a	n/a
17	CTCF	chr12:2031737-2031916	GM19239	blood:	n/a	chr12:2031831-2031849 chr12:2031832-2031848
18	CTCF	chr12:2030289-2030380	GM19238	blood:	n/a	chr12:2030323-2030336
19	CTCF	chr12:2030203-2030423	GM19239	blood:	n/a	chr12:2030323-2030336
20	CTCF	chr12:2031240-2031390	NB4	blood:	n/a	n/a
21	CTCF	chr12:2031236-2031415	GM13976	blood:	n/a	n/a
22	CTCF	chr12:2030293-2030375	GM12891	blood:	n/a	chr12:2030323-2030336
23	CTCF	chr12:2031220-2031370	HBMEC	blood vessel:	n/a	n/a
24	CTCF	chr12:2030220-2030370	GM12874	blood:	n/a	chr12:2030323-2030336
25	CTCF	chr12:2031280-2031430	HCFaa	heart:	n/a	n/a
26	CTCF	chr12:2030240-2030390	NB4	blood:	n/a	chr12:2030323-2030336
27	CTCF	chr12:2031680-2031830	HRE	kidney:	n/a	n/a
28	CTCF	chr12:2031819-2031824	H1-hESC	embryonic stem cell:	n/a	n/a
29	CTCF	chr12:2031240-2031390	GM12866	blood:	n/a	n/a
30	CTCF	chr12:2031180-2031330	HBMEC	blood vessel:	n/a	n/a
31	CTCF	chr12:2031280-2031430	GM12873	blood:	n/a	n/a
32	CTCF	chr12:2031595-2031731	GM19239	blood:	n/a	n/a
33	CTCF	chr12:2031700-2031850	HepG2	liver:	n/a	chr12:2031831-2031849 chr12:2031832-2031848
34	CTCF	chr12:2030140-2030290	HL-60	blood:	n/a	n/a
35	CTCF	chr12:2030300-2030450	GM12867	blood:	n/a	chr12:2030323-2030336
36	CTCF	chr12:2031200-2031350	GM12867	blood:	n/a	n/a
37	CTCF	chr12:2031240-2031390	HRE	kidney:	n/a	n/a
38	CTCF	chr12:2031240-2031390	GM12873	blood:	n/a	n/a
39	CTCFL	chr12:2031721-2031854	K562	blood:	n/a	n/a
40	HMGN3	chr12:2031274-2031451	K562	blood:	n/a	n/a
41	MAX	chr12:2029676-2029801	NB4	blood:	n/a	n/a
42	MAX	chr12:2030120-2030514	NB4	blood:	n/a	n/a
43	MYC	chr12:2030121-2030491	NB4	blood:	n/a	n/a
44	POLR2A	chr12:2031105-2031912	GM15510	blood:	n/a	n/a
45	POLR2A	chr12:2030053-2030580	HL-60	blood:	n/a	n/a
46	POLR2A	chr12:2030273-2030289	MCF-7	breast:	n/a	n/a
47	POLR2A	chr12:2030332-2030352	MCF-7	breast:	n/a	n/a
48	POLR2A	chr12:2030320-2030326	MCF-7	breast:	n/a	n/a
49	POLR2A	chr12:2030208-2030267	MCF-7	breast:	n/a	n/a
50	RAD21	chr12:2031176-2031523	H1-hESC	embryonic stem cell:	n/a	n/a

(count:671 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:2029051-2029101	Hela-S3	cervix:	n/a
2	chr12:2030178-2030228	Hepatocyte	liver:	n/a
3	chr12:2032495-2032545	SAEC	small airway:	n/a
4	chr12:2031546-2031596	HEK293	kidney:	embryo
5	chr12:2029751-2029801	BJ	skin:	n/a
6	chr12:2029751-2029801	HL-60	blood:	n/a
7	chr12:2032495-2032545	U87	brain:	n/a
8	chr12:2031417-2031467	NH-A	brain:	n/a
9	chr12:2030223-2030273	SKMC	muscle:	n/a
10	chr12:2031922-2031972	PFSK-1	brain:	n/a
11	chr12:2031546-2031596	SK-N-MC	brain:	n/a
12	chr12:2029751-2029801	GM19239	blood:	n/a
13	chr12:2032495-2032545	NH-A	brain:	n/a
14	chr12:2030178-2030228	K562	blood:	n/a
15	chr12:2029051-2029101	ECC-1	luminal epithelium:	n/a
16	chr12:2031417-2031467	SK-N-MC	brain:	n/a
17	chr12:2030200-2030250	U87	brain:	n/a
18	chr12:2029051-2029101	HCM	heart:	n/a
19	chr12:2030223-2030273	GM06990	blood:	n/a
20	chr12:2032495-2032545	AG09319	gingival:	n/a
21	chr12:2029830-2029880	HMEC	breast:	n/a
22	chr12:2031546-2031596	IMR90	lung:	fetal
23	chr12:2032460-2032510	SK-N-SH	brain:	n/a
24	chr12:2030178-2030228	Jurkat	blood:	n/a
25	chr12:2029051-2029101	HMEC	breast:	n/a
26	chr12:2029830-2029880	AG09319	gingival:	n/a
27	chr12:2032460-2032510	AG09319	gingival:	n/a
28	chr12:2032460-2032510	HRPEpiC	eye:	n/a
29	chr12:2032460-2032510	MCF-7	breast:	n/a
30	chr12:2029751-2029801	MCF10A-Er-Src	breast:	n/a
31	chr12:2029751-2029801	LNCaP	prostate:	n/a
32	chr12:2032495-2032545	GM06990	blood:	n/a
33	chr12:2031417-2031467	CMK	blood:	n/a
34	chr12:2032495-2032545	LNCaP	prostate:	n/a
35	chr12:2030178-2030228	HRPEpiC	eye:	n/a
36	chr12:2032460-2032510	HPAEpiC	pulmonary alveolar:	n/a
37	chr12:2032495-2032545	AoSMC	blood vessel:	n/a
38	chr12:2031922-2031972	A549	lung:	n/a
39	chr12:2030178-2030228	T-47D	breast:	n/a
40	chr12:2031922-2031972	NT2-D1	testis:	n/a
41	chr12:2030223-2030273	AoSMC	blood vessel:	n/a
42	chr12:2031417-2031467	Jurkat	blood:	n/a
43	chr12:2031546-2031596	SKMC	muscle:	n/a
44	chr12:2029051-2029101	HCT-116	colon:	n/a
45	chr12:2029830-2029880	GM12891	blood:	n/a
46	chr12:2030178-2030228	HPAEpiC	pulmonary alveolar:	n/a
47	chr12:2031417-2031467	ProgFib	skin:	n/a
48	chr12:2029830-2029880	GM12878	blood:	n/a
49	chr12:2030200-2030250	NH-A	brain:	n/a
50	chr12:2029830-2029880	AG04449	skin:	fetal

(count:6 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:2023041..2025540-chr12:2026529..2030092,4	K562	blood:
2	chr12:2030801..2033183-chr12:2135415..2137754,2	K562	blood:
3	chr12:2031497..2033702-chr12:2034119..2036630,3	MCF-7	breast:
4	chr12:2025078..2027565-chr12:2030065..2032960,2	MCF-7	breast:
5	chr12:2028759..2031079-chr12:2033519..2035099,2	K562	blood:
6	chr12:2032329..2034362-chr12:2036724..2039438,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CACNA1C-1	chr12:2027014-2029505	NONHSAT025434
2	lnc-CACNA1C-1	chr12:2031798-2032033	ENSG00000256706.1

No data

Variant related genes	Relation type
CACNA2D4	TF binding region
CACNA2D4	CpG island
ENSG00000151062	chromatin interactions
ENSG00000256706	chromatin interactions

Extended variants
information (count: 168 )
Associated
traits (count: 80 )

Variant overlapped rSNPs/rCNVs (count:168 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs192892082	chr12:2028796-2028797	Enhancers Weak transcription Genic enhancers Active TSS Flanking Active TSS	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
2	rs559908896	chr12:2028811-2028812	Weak transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
3	rs550685294	chr12:2028825-2028826	Weak transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
4	rs116749283	chr12:2028844-2028845	Weak transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
5	rs150590767	chr12:2028862-2028863	Weak transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
6	rs552368747	chr12:2028877-2028878	Weak transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
7	rs185438724	chr12:2028974-2028975	Weak transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
8	rs570416760	chr12:2029020-2029021	Weak transcription Genic enhancers Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
9	rs568778304	chr12:2029032-2029033	Weak transcription Genic enhancers Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
10	rs571075018	chr12:2029052-2029053	Weak transcription Genic enhancers Enhancers	CpG island Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
11	rs117737398	chr12:2029075-2029076	Weak transcription Genic enhancers Enhancers	CpG island Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
12	rs546884087	chr12:2029142-2029143	Weak transcription Genic enhancers Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
13	rs79638473	chr12:2029152-2029153	Weak transcription Genic enhancers Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
14	rs535595544	chr12:2029239-2029240	Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
15	rs11062022	chr12:2029258-2029259	Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs568107414	chr12:2029404-2029405	Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
17	rs190316712	chr12:2029413-2029414	Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
18	rs536936233	chr12:2029462-2029463	Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
19	rs151286845	chr12:2029494-2029495	Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
20	rs182489136	chr12:2029495-2029496	Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
21	rs140662475	chr12:2029501-2029502	Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
22	rs374794464	chr12:2029529-2029530	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs386759502	chr12:2029530-2029531	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs76018383	chr12:2029531-2029532	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs561904064	chr12:2029532-2029533	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs367607570	chr12:2029533-2029534	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs201867265	chr12:2029535-2029536	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs200054470	chr12:2029537-2029538	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs201032523	chr12:2029538-2029539	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs184964913	chr12:2029550-2029551	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs533025701	chr12:2029558-2029559	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs551102033	chr12:2029567-2029568	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs188212022	chr12:2029576-2029577	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs144615696	chr12:2029619-2029620	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs547266045	chr12:2029623-2029624	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs377714114	chr12:2029632-2029633	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs568341018	chr12:2029642-2029643	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs543965659	chr12:2029644-2029645	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs550726509	chr12:2029665-2029666	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs367818184	chr12:2029698-2029699	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs569016943	chr12:2029703-2029704	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs539874044	chr12:2029709-2029710	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs2429169	chr12:2029737-2029738	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs566849128	chr12:2029750-2029751	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs374743987	chr12:2029770-2029771	Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs555679673	chr12:2029814-2029815	Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs573954864	chr12:2029821-2029822	Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs147887471	chr12:2029834-2029835	Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs556355157	chr12:2029837-2029838	Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs577669287	chr12:2029846-2029847	Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:80)

Disease	PMID	Source
Myelofibrosis	22110671	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Glaucoma	21310917	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Malignant peripheral nerve sheath tumor	19844265	CNVD
Squamous cell cancer	19607727	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	17133270	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Mental retardation	17847001	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
abnormal development	18461090	CNVD
Ovarian cancer	20844748	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Medulloblastoma	16968546	CNVD
Ovine squamous-cell carcinoma	17599052	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
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21509527	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21785460	CNVD
Ovarian cancer	21720365	CNVD
Myelodysplastic syndrome	21251322	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Cancer	20164919	CNVD
Urothelial carcinoma	21177765	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:132 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:2022600-2028800	Enhancers	Fetal Heart	heart
2	chr12:2024000-2029000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
3	chr12:2026000-2028800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
4	chr12:2026400-2028800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr12:2026600-2030200	Weak transcription	Pancreas	Pancrea
6	chr12:2026600-2031600	Weak transcription	Gastric	stomach
7	chr12:2026800-2028800	Active TSS	Rectal Mucosa Donor 29	rectum
8	chr12:2026800-2033600	Weak transcription	Brain Inferior Temporal Lobe	brain
9	chr12:2027200-2033800	Weak transcription	Colon Smooth Muscle	Colon
10	chr12:2027400-2028800	Enhancers	K562	blood
11	chr12:2027600-2029000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
12	chr12:2027600-2033600	Weak transcription	Left Ventricle	heart
13	chr12:2027600-2033600	Weak transcription	Right Ventricle	heart
14	chr12:2027600-2041800	Weak transcription	Fetal Brain Female	brain
15	chr12:2027800-2028800	Enhancers	Fetal Muscle Trunk	muscle
16	chr12:2027800-2028800	Enhancers	Skeletal Muscle Male	skeletal muscle
17	chr12:2027800-2029000	Enhancers	Primary hematopoietic stem cells	blood
18	chr12:2027800-2029000	Enhancers	Fetal Muscle Leg	muscle
19	chr12:2027800-2029200	Enhancers	Fetal Thymus	thymus
20	chr12:2027800-2029200	Enhancers	Skeletal Muscle Female	skeletal muscle
21	chr12:2027800-2033800	Weak transcription	Spleen	Spleen
22	chr12:2028000-2028800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
23	chr12:2028000-2028800	Enhancers	Thymus	Thymus
24	chr12:2028000-2029200	Enhancers	Primary B cells from cord blood	blood
25	chr12:2028000-2030400	Weak transcription	Rectal Smooth Muscle	rectum
26	chr12:2028200-2028800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
27	chr12:2028200-2028800	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
28	chr12:2028200-2030000	Weak transcription	Adipose Nuclei	Adipose
29	chr12:2028200-2030200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
30	chr12:2028200-2030200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
31	chr12:2028400-2031400	Enhancers	Primary hematopoietic stem cells short term culture	blood
32	chr12:2028400-2033600	Weak transcription	Brain Anterior Caudate	brain
33	chr12:2028400-2033600	Weak transcription	Psoas Muscle	Psoas
34	chr12:2028600-2028800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
35	chr12:2028600-2028800	Enhancers	Primary neutrophils fromperipheralblood	blood
36	chr12:2028600-2029000	Enhancers	Primary B cells from peripheral blood	blood
37	chr12:2028600-2029200	Genic enhancers	Primary monocytes fromperipheralblood	blood
38	chr12:2028600-2029800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
39	chr12:2028600-2030200	Weak transcription	Placenta	Placenta
40	chr12:2028800-2029800	Weak transcription	Primary neutrophils fromperipheralblood	blood
41	chr12:2028800-2029800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
42	chr12:2028800-2029800	Weak transcription	Thymus	Thymus
43	chr12:2028800-2030000	Weak transcription	Fetal Muscle Trunk	muscle
44	chr12:2028800-2030000	Weak transcription	Rectal Mucosa Donor 29	rectum
45	chr12:2028800-2031600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
46	chr12:2028800-2032200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
47	chr12:2028800-2032600	Weak transcription	Fetal Heart	heart
48	chr12:2028800-2033600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr12:2028800-2033600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
50	chr12:2028800-2041000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain

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