Variant report

Variant	nsv1043329
Chromosome Location	chr12:1986238-2034887
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:369)
CpG islands
(count:1588)
Chromatin interactive
region (count:18)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:369 , 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	ATF1	chr12:2026800-2027171	K562	blood:	n/a	n/a
2	BATF	chr12:2033456-2033699	GM12878	blood:	n/a	n/a
3	BATF	chr12:2033447-2033715	GM12878	blood:	n/a	n/a
4	BCL11A	chr12:2033453-2033998	GM12878	blood:	n/a	chr12:2033562-2033571
5	BCLAF1	chr12:2033516-2033761	GM12878	blood:	n/a	chr12:2033562-2033571
6	BHLHE40	chr12:1994817-1995132	K562	blood:	n/a	n/a
7	BHLHE40	chr12:2031760-2031813	K562	blood:	n/a	n/a
8	BHLHE40	chr12:2024905-2027201	K562	blood:	n/a	n/a
9	BHLHE40	chr12:2016799-2017045	HepG2	liver:	n/a	n/a
10	BHLHE40	chr12:1991971-1992232	K562	blood:	n/a	n/a
11	BHLHE40	chr12:2033498-2033987	GM12878	blood:	n/a	n/a
12	CCNT2	chr12:2025683-2026350	K562	blood:	n/a	chr12:2025757-2025777
13	CCNT2	chr12:2026862-2027199	K562	blood:	n/a	chr12:2027030-2027050
14	CEBPB	chr12:1999999-2000347	Hela-S3	cervix:	n/a	chr12:2000179-2000190
15	CEBPB	chr12:1999997-2000357	K562	blood:	n/a	chr12:2000179-2000190
16	CEBPB	chr12:2026198-2026326	K562	blood:	n/a	n/a
17	CEBPB	chr12:1999999-2000353	A549	lung:	n/a	chr12:2000179-2000190
18	CEBPB	chr12:1999979-2000288	MCF-7	breast:	n/a	chr12:2000179-2000190
19	CEBPB	chr12:2008040-2008211	K562	blood:	n/a	chr12:2008173-2008184
20	CEBPB	chr12:2006437-2006656	HepG2	liver:	n/a	chr12:2006517-2006528
21	CEBPB	chr12:2000047-2000334	IMR90	lung:	n/a	chr12:2000179-2000190
22	CEBPB	chr12:2000023-2000347	H1-hESC	embryonic stem cell:	n/a	chr12:2000179-2000190
23	CEBPB	chr12:2008049-2008258	HepG2	liver:	n/a	chr12:2008173-2008184
24	CEBPB	chr12:2000004-2000354	HepG2	liver:	n/a	chr12:2000179-2000190
25	CEBPB	chr12:2008053-2008313	IMR90	lung:	n/a	chr12:2008173-2008184
26	CEBPB	chr12:2006370-2006679	IMR90	lung:	n/a	chr12:2006517-2006528
27	CEBPB	chr12:1999987-2000369	HepG2	liver:	n/a	chr12:2000179-2000190
28	CEBPB	chr12:2006422-2006699	A549	lung:	n/a	chr12:2006517-2006528
29	CTCF	chr12:2030270-2030390	Spleen_OC	spleen:	n/a	chr12:2030323-2030336
30	CTCF	chr12:2031220-2031370	HBMEC	blood vessel:	n/a	n/a
31	CTCF	chr12:2031265-2031393	Fibrobl	skin:	n/a	n/a
32	CTCF	chr12:2030220-2030370	GM12873	blood:	n/a	chr12:2030323-2030336
33	CTCF	chr12:2031280-2031430	HUVEC	blood vessel:	n/a	n/a
34	CTCF	chr12:2030289-2030380	GM19238	blood:	n/a	chr12:2030323-2030336
35	CTCF	chr12:2031680-2031830	HRE	kidney:	n/a	n/a
36	CTCF	chr12:2031222-2031411	GM19238	blood:	n/a	n/a
37	CTCF	chr12:2031301-2031343	GM10266	blood:	n/a	n/a
38	CTCF	chr12:2026182-2026309	K562	blood:	n/a	n/a
39	CTCF	chr12:2031240-2031390	NB4	blood:	n/a	n/a
40	CTCF	chr12:2031257-2031393	H1-hESC	embryonic stem cell:	n/a	n/a
41	CTCF	chr12:2011957-2012055	Lung_OC	lung:	n/a	n/a
42	CTCF	chr12:2031180-2031330	HBMEC	blood vessel:	n/a	n/a
43	CTCF	chr12:2024540-2024690	NB4	blood:	n/a	n/a
44	CTCF	chr12:2031240-2031390	HRE	kidney:	n/a	n/a
45	CTCF	chr12:2031800-2031950	GM12873	blood:	n/a	chr12:2031831-2031849 chr12:2031832-2031848
46	CTCF	chr12:2031754-2031883	HepG2	liver:	n/a	chr12:2031831-2031849 chr12:2031832-2031848
47	CTCF	chr12:2024560-2024710	HepG2	liver:	n/a	chr12:2024697-2024710
48	CTCF	chr12:2030140-2030290	HL-60	blood:	n/a	n/a
49	CTCF	chr12:2030176-2030363	K562	blood:	n/a	chr12:2030323-2030336
50	CTCF	chr12:2031240-2031390	GM12873	blood:	n/a	n/a

(count:1588 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:2017134-2017184	MCF-7	breast:	n/a
2	chr12:2028355-2028405	Hela-S3	cervix:	n/a
3	chr12:2017134-2017184	MCF-7	breast:	n/a
4	chr12:2028355-2028405	Hela-S3	cervix:	n/a
5	chr12:2029830-2029880	HEEpiC	esophagus:	n/a
6	chr12:2031546-2031596	GM12892	blood:	n/a
7	chr12:2028355-2028405	HMEC	breast:	n/a
8	chr12:2027993-2028043	PrEC	prostate:	n/a
9	chr12:2028475-2028525	SK-N-SH_RA	brain:	n/a
10	chr12:2029051-2029101	RPTEC	kidney:	n/a
11	chr12:2028254-2028304	HRCEpiC	kidney:	n/a
12	chr12:2014983-2015033	AG04449	skin:	fetal
13	chr12:2030223-2030273	PANC-1	pancreas:	n/a
14	chr12:2028475-2028525	GM19239	blood:	n/a
15	chr12:2031922-2031972	A549	lung:	n/a
16	chr12:2027993-2028043	A549	lung:	n/a
17	chr12:2027805-2027855	SK-N-MC	brain:	n/a
18	chr12:2017093-2017143	ProgFib	skin:	n/a
19	chr12:2014983-2015033	HCT-116	colon:	n/a
20	chr12:2021945-2021995	AoSMC	blood vessel:	n/a
21	chr12:2030200-2030250	GM12892	blood:	n/a
22	chr12:2031417-2031467	AG04450	lung:	fetal
23	chr12:2017649-2017699	K562	blood:	n/a
24	chr12:2018050-2018100	Hepatocyte	liver:	n/a
25	chr12:2018050-2018100	AG04449	skin:	fetal
26	chr12:2018144-2018194	SK-N-SH_RA	brain:	n/a
27	chr12:2018144-2018194	HUVEC	blood vessel:	n/a
28	chr12:2017746-2017796	HEEpiC	esophagus:	n/a
29	chr12:2028254-2028304	BE2_C	brain:	n/a
30	chr12:2032460-2032510	HL-60	blood:	n/a
31	chr12:2018144-2018194	AG09309	skin:	n/a
32	chr12:2018864-2018914	HRPEpiC	eye:	n/a
33	chr12:2027805-2027855	GM12891	blood:	n/a
34	chr12:2028475-2028525	HEEpiC	esophagus:	n/a
35	chr12:2017510-2017560	HCF	heart:	n/a
36	chr12:2032495-2032545	HPAEpiC	pulmonary alveolar:	n/a
37	chr12:2028254-2028304	GM12891	blood:	n/a
38	chr12:2029830-2029880	HPAEpiC	pulmonary alveolar:	n/a
39	chr12:2029051-2029101	HAEpiC	amniotic membrane:	n/a
40	chr12:2018864-2018914	A549	lung:	n/a
41	chr12:2032495-2032545	SK-N-SH_RA	brain:	n/a
42	chr12:2018050-2018100	AG04450	lung:	fetal
43	chr12:2017746-2017796	IMR90	lung:	fetal
44	chr12:2028254-2028304	IMR90	lung:	fetal
45	chr12:2031922-2031972	SK-N-MC	brain:	n/a
46	chr12:2017093-2017143	GM19239	blood:	n/a
47	chr12:2017093-2017143	NT2-D1	testis:	n/a
48	chr12:2028254-2028304	CMK	blood:	n/a
49	chr12:2017134-2017184	GM12878	blood:	n/a
50	chr12:2030178-2030228	NB4	blood:	n/a

(count:18 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:2025078..2027565-chr12:2030065..2032960,2	MCF-7	breast:
2	chr12:2028759..2031079-chr12:2033519..2035099,2	K562	blood:
3	chr12:1947445..1949197-chr12:2016726..2018832,2	MCF-7	breast:
4	chr12:2030801..2033183-chr12:2135415..2137754,2	K562	blood:
5	chr12:2031497..2033702-chr12:2034119..2036630,3	MCF-7	breast:
6	chr12:1982062..1983660-chr12:1991935..1993547,2	MCF-7	breast:
7	chr12:1994373..1995913-chr12:1997731..2000184,2	K562	blood:
8	chr12:1947774..1950374-chr12:1986873..1988503,2	MCF-7	breast:
9	chr12:2031497..2033702-chr12:2034119..2036630,3	MCF-7	breast:
10	chr12:2032329..2034362-chr12:2036724..2039438,2	MCF-7	breast:
11	chr12:1911026..1914378-chr12:2033211..2036733,3	MCF-7	breast:
12	chr12:2024067..2025743-chr12:2043687..2046563,2	MCF-7	breast:
13	chr12:2023041..2025540-chr12:2026529..2030092,4	K562	blood:
14	chr12:1962744..1965202-chr12:1987725..1990187,2	MCF-7	breast:
15	chr12:2023041..2025540-chr12:2026529..2030092,4	K562	blood:
16	chr12:2028759..2031079-chr12:2033519..2035099,2	K562	blood:
17	chr12:1994373..1995913-chr12:1997731..2000184,2	K562	blood:
18	chr12:1976877..1978383-chr12:1995618..1998420,2	MCF-7	breast:

(count:3 , 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
3	lnc-CACNA1C-1	chr12:2027117-2027195	ENSG00000256706.1

No data

Variant related genes	Relation type
ENSG00000256706	TF binding region
CACNA2D4	TF binding region
ENSG00000256706	CpG island
CACNA2D4	CpG island
ENSG00000151062	chromatin interactions
ENSG00000256706	chromatin interactions
ENSG00000235049	chromatin interactions

Extended variants
information (count: 1488 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:1488 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs533572406	chr12:1986239-1986240	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
2	rs16928861	chr12:1986278-1986279	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
3	rs114190592	chr12:1986341-1986342	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
4	rs527760630	chr12:1986375-1986376	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
5	rs549040149	chr12:1986401-1986402	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
6	rs113047238	chr12:1986499-1986500	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
7	rs567339339	chr12:1986541-1986542	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
8	rs537682997	chr12:1986579-1986580	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
9	rs183904688	chr12:1986601-1986602	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs149179510	chr12:1986606-1986607	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs73032431	chr12:1986638-1986639	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs538866736	chr12:1986661-1986662	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs546477581	chr12:1986665-1986666	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs143341590	chr12:1986710-1986711	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs115870743	chr12:1986743-1986744	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs553686241	chr12:1986746-1986747	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs188794419	chr12:1986782-1986783	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs571950702	chr12:1986784-1986785	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs369046303	chr12:1986857-1986858	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs554669773	chr12:1986882-1986883	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs576113763	chr12:1986885-1986886	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs371018312	chr12:1986891-1986892	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs563240354	chr12:1986955-1986956	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs183719247	chr12:1986968-1986969	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs374152632	chr12:1986978-1986979	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs545614012	chr12:1987000-1987001	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs377624466	chr12:1987031-1987032	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs7297190	chr12:1987044-1987045	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs11615011	chr12:1987074-1987075	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs74360003	chr12:1987081-1987082	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs577498123	chr12:1987155-1987156	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs151311000	chr12:1987172-1987173	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs528080624	chr12:1987175-1987176	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs7308134	chr12:1987245-1987246	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	disease
35	rs549897447	chr12:1987250-1987251	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs140595785	chr12:1987313-1987314	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs538534209	chr12:1987342-1987343	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs374395390	chr12:1987349-1987350	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs372287693	chr12:1987425-1987426	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs34323075	chr12:1987443-1987444	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs375571644	chr12:1987454-1987455	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs150490866	chr12:1987477-1987478	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs376257275	chr12:1987489-1987490	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs186895987	chr12:1987496-1987497	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs375871662	chr12:1987538-1987539	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs371701676	chr12:1987544-1987545	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs191673995	chr12:1987571-1987572	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs376230695	chr12:1987578-1987579	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs368763964	chr12:1987579-1987580	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs79680317	chr12:1987605-1987606	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:81)

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
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:576 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:1980600-1988600	Weak transcription	Right Atrium	heart
2	chr12:1981000-1986800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr12:1981000-1992000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr12:1985800-1986600	Bivalent Enhancer	HepG2	liver
5	chr12:1986600-1987400	Enhancers	HepG2	liver
6	chr12:1986800-1987000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr12:1987800-1988000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr12:1989000-1990600	Enhancers	Fetal Muscle Leg	muscle
9	chr12:1989000-1991400	Enhancers	Fetal Muscle Trunk	muscle
10	chr12:1989200-1989400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr12:1989200-1989400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
12	chr12:1989200-1989400	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
13	chr12:1989200-1990200	Bivalent Enhancer	HepG2	liver
14	chr12:1989400-1995600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
15	chr12:1989800-1990200	Enhancers	K562	blood
16	chr12:1990200-1994200	Weak transcription	K562	blood
17	chr12:1992000-1993000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr12:1992400-1992800	Enhancers	Monocytes-CD14+_RO01746	blood
19	chr12:1993000-1997000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
20	chr12:1993200-1993400	Bivalent Enhancer	Fetal Stomach	stomach
21	chr12:1993200-1993400	Bivalent Enhancer	Stomach Smooth Muscle	stomach
22	chr12:1993200-1993600	Enhancers	Fetal Muscle Leg	muscle
23	chr12:1993200-1993800	Bivalent Enhancer	IMR90 fetal lung fibroblasts Cell Line	lung
24	chr12:1993800-1996000	Enhancers	Stomach Mucosa	stomach
25	chr12:1994000-1996000	Enhancers	Gastric	stomach
26	chr12:1994200-1995000	Enhancers	HepG2	liver
27	chr12:1994200-1996000	Enhancers	K562	blood
28	chr12:1994800-1995400	Enhancers	Rectal Mucosa Donor 31	rectum
29	chr12:1995000-1995400	Enhancers	Pancreas	Pancrea
30	chr12:1995000-1995400	Flanking Active TSS	HepG2	liver
31	chr12:1995400-1995800	Enhancers	HepG2	liver
32	chr12:1995600-1995800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
33	chr12:1995800-1996000	Enhancers	H9 Cell Line	embryonic stem cell
34	chr12:1997000-1997400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
35	chr12:1997400-1999400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
36	chr12:1999400-2000200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
37	chr12:1999800-2000000	Bivalent Enhancer	Placenta	Placenta
38	chr12:2000000-2000400	Enhancers	Monocytes-CD14+_RO01746	blood
39	chr12:2000000-2000600	ZNF genes & repeats	Primary monocytes fromperipheralblood	blood
40	chr12:2000600-2001200	Weak transcription	Primary monocytes fromperipheralblood	blood
41	chr12:2001200-2001400	Enhancers	Primary monocytes fromperipheralblood	blood
42	chr12:2015600-2016800	Enhancers	Skeletal Muscle Male	skeletal muscle
43	chr12:2016000-2017200	Enhancers	Right Ventricle	heart
44	chr12:2016200-2017600	Enhancers	Skeletal Muscle Female	skeletal muscle
45	chr12:2016400-2017000	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
46	chr12:2016400-2017200	ZNF genes & repeats	Primary neutrophils fromperipheralblood	blood
47	chr12:2016600-2016800	Bivalent/Poised TSS	A549	lung
48	chr12:2016600-2017600	Bivalent Enhancer	Fetal Muscle Leg	muscle
49	chr12:2016800-2017000	ZNF genes & repeats	Primary T helper cells PMA-I stimulated	--
50	chr12:2016800-2017000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--

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