Variant report

Variant	nsv1045408
Chromosome Location	chr12:40620554-40664424
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:334)
CpG islands
(count:122)
Chromatin interactive
region (count:8)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:334 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr12:40656311-40656835	GM12878	blood:	n/a	n/a
2	ATF2	chr12:40656402-40656862	GM12878	blood:	n/a	n/a
3	ATF2	chr12:40626340-40626772	GM12878	blood:	n/a	n/a
4	ATF2	chr12:40655686-40656207	GM12878	blood:	n/a	n/a
5	ATF2	chr12:40655786-40656165	GM12878	blood:	n/a	n/a
6	ATF2	chr12:40626439-40626762	GM12878	blood:	n/a	n/a
7	BATF	chr12:40655828-40656026	GM12878	blood:	n/a	chr12:40655963-40655974
8	BATF	chr12:40656446-40656805	GM12878	blood:	n/a	n/a
9	BATF	chr12:40620474-40620707	GM12878	blood:	n/a	chr12:40620577-40620588
10	BATF	chr12:40656440-40656787	GM12878	blood:	n/a	n/a
11	BATF	chr12:40655840-40656023	GM12878	blood:	n/a	chr12:40655963-40655974
12	BCL11A	chr12:40656391-40656827	GM12878	blood:	n/a	n/a
13	BCL11A	chr12:40656497-40656736	GM12878	blood:	n/a	n/a
14	BCLAF1	chr12:40656342-40656718	GM12878	blood:	n/a	n/a
15	BHLHE40	chr12:40655843-40656217	GM12878	blood:	n/a	n/a
16	BHLHE40	chr12:40656510-40656885	GM12878	blood:	n/a	n/a
17	CBX3	chr12:40642410-40642763	HCT-116	colon:	n/a	n/a
18	CEBPB	chr12:40630189-40630363	H1-hESC	embryonic stem cell:	n/a	chr12:40630267-40630278
19	CEBPB	chr12:40631962-40632642	Hela-S3	cervix:	n/a	chr12:40632271-40632284
20	CEBPB	chr12:40621180-40621515	A549	lung:	n/a	chr12:40621347-40621358
21	CEBPB	chr12:40637428-40637679	HepG2	liver:	n/a	chr12:40637648-40637660 chr12:40637549-40637562 chr12:40637549-40637560 chr12:40637549-40637562
22	CEBPB	chr12:40657459-40657766	IMR90	lung:	n/a	n/a
23	CEBPB	chr12:40630141-40630428	K562	blood:	n/a	chr12:40630267-40630278
24	CEBPB	chr12:40633038-40633067	A549	lung:	n/a	n/a
25	CEBPB	chr12:40649106-40649333	HepG2	liver:	n/a	n/a
26	CEBPB	chr12:40621221-40621449	HepG2	liver:	n/a	chr12:40621347-40621358
27	CEBPB	chr12:40658977-40659258	IMR90	lung:	n/a	n/a
28	CEBPB	chr12:40630137-40630417	HepG2	liver:	n/a	chr12:40630267-40630278
29	CEBPB	chr12:40627874-40628082	HepG2	liver:	n/a	chr12:40627988-40627999 chr12:40627987-40627998
30	CEBPB	chr12:40623556-40623808	A549	lung:	n/a	n/a
31	CEBPB	chr12:40627858-40628014	H1-hESC	embryonic stem cell:	n/a	chr12:40627988-40627999 chr12:40627987-40627998
32	CEBPB	chr12:40621177-40621516	IMR90	lung:	n/a	chr12:40621347-40621358
33	CEBPB	chr12:40632127-40632489	A549	lung:	n/a	chr12:40632271-40632284
34	CHD1	chr12:40656188-40656592	GM12878	blood:	n/a	n/a
35	CHD1	chr12:40622605-40622717	GM12878	blood:	n/a	n/a
36	CHD1	chr12:40617719-40620681	GM12878	blood:	n/a	chr12:40618748-40618758
37	CHD2	chr12:40619992-40620786	GM12878	blood:	n/a	n/a
38	CHD2	chr12:40655781-40656799	GM12878	blood:	n/a	n/a
39	CREB1	chr12:40620485-40620823	A549	lung:	n/a	n/a
40	CREB1	chr12:40620379-40620792	A549	lung:	n/a	n/a
41	CTCF	chr12:40622640-40622790	HepG2	liver:	n/a	n/a
42	CTCF	chr12:40663160-40663310	HEEpiC	esophagus:	n/a	n/a
43	CTCF	chr12:40663000-40663150	AG10803	skin:	n/a	n/a
44	CTCF	chr12:40662949-40663280	MCF-7	breast:	n/a	n/a
45	CTCF	chr12:40662900-40663050	HMEC	breast:	n/a	n/a
46	CTCF	chr12:40663060-40663210	GM12871	blood:	n/a	n/a
47	CTCF	chr12:40622720-40622870	GM12869	blood:	n/a	n/a
48	CTCF	chr12:40663080-40663230	HCT-116	colon:	n/a	n/a
49	CTCF	chr12:40621160-40621310	RPTEC	kidney:	n/a	n/a
50	CTCF	chr12:40663078-40663169	Hela-S3	cervix:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:40645170-40645220	AG04450	lung:	fetal
2	chr12:40622688-40622738	LNCaP	prostate:	n/a
3	chr12:40622688-40622738	Jurkat	blood:	n/a
4	chr12:40622688-40622738	HNPCEpiC	eye:	n/a
5	chr12:40645170-40645220	HL-60	blood:	n/a
6	chr12:40645170-40645220	HCF	heart:	n/a
7	chr12:40622688-40622738	HMEC	breast:	n/a
8	chr12:40622688-40622738	AG09309	skin:	n/a
9	chr12:40645170-40645220	GM12891	blood:	n/a
10	chr12:40645170-40645220	NHDF-neo	bronchial:	n/a
11	chr12:40622688-40622738	K562	blood:	n/a
12	chr12:40645170-40645220	T-47D	breast:	n/a
13	chr12:40645170-40645220	PrEC	prostate:	n/a
14	chr12:40622688-40622738	HEEpiC	esophagus:	n/a
15	chr12:40622688-40622738	AG04450	lung:	fetal
16	chr12:40645170-40645220	A549	lung:	n/a
17	chr12:40622688-40622738	RPTEC	kidney:	n/a
18	chr12:40622688-40622738	AG10803	skin:	n/a
19	chr12:40645170-40645220	HCT-116	colon:	n/a
20	chr12:40622688-40622738	AoSMC	blood vessel:	n/a
21	chr12:40645170-40645220	HUVEC	blood vessel:	n/a
22	chr12:40622688-40622738	A549	lung:	n/a
23	chr12:40622688-40622738	HCT-116	colon:	n/a
24	chr12:40645170-40645220	NT2-D1	testis:	n/a
25	chr12:40645170-40645220	PFSK-1	brain:	n/a
26	chr12:40622688-40622738	HCPEpiC	choroid plexus:	n/a
27	chr12:40645170-40645220	K562	blood:	n/a
28	chr12:40645170-40645220	ovcar-3	ovarian:	n/a
29	chr12:40645170-40645220	GM12878	blood:	n/a
30	chr12:40622688-40622738	NH-A	brain:	n/a
31	chr12:40645170-40645220	RPTEC	kidney:	n/a
32	chr12:40645170-40645220	H1-hESC	embryonic stem cell:	embryo
33	chr12:40645170-40645220	HIPEpiC	eye:	n/a
34	chr12:40645170-40645220	U87	brain:	n/a
35	chr12:40622688-40622738	HepG2	liver:	n/a
36	chr12:40622688-40622738	GM12891	blood:	n/a
37	chr12:40622688-40622738	NHDF-neo	bronchial:	n/a
38	chr12:40645170-40645220	SK-N-MC	brain:	n/a
39	chr12:40622688-40622738	H1-hESC	embryonic stem cell:	embryo
40	chr12:40622688-40622738	HCM	heart:	n/a
41	chr12:40645170-40645220	GM06990	blood:	n/a
42	chr12:40645170-40645220	HRE	kidney:	n/a
43	chr12:40622688-40622738	U87	brain:	n/a
44	chr12:40622688-40622738	CMK	blood:	n/a
45	chr12:40645170-40645220	HMEC	breast:	n/a
46	chr12:40645170-40645220	NHBE	bronchial:	n/a
47	chr12:40622688-40622738	HPAEpiC	pulmonary alveolar:	n/a
48	chr12:40645170-40645220	SK-N-SH_RA	brain:	n/a
49	chr12:40622688-40622738	GM19239	blood:	n/a
50	chr12:40622688-40622738	NHBE	bronchial:	n/a

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:40658480..40661049-chr12:40663809..40666158,2	MCF-7	breast:
2	chr1:153939261..153941119-chr12:40643887..40646371,2	MCF-7	breast:
3	12:40642938-40650987..12:40793507-40812339	K562	blood:
4	chr12:40619170..40621140-chr12:40621940..40624766,2	MCF-7	breast:
5	chr12:40658480..40661049-chr12:40663809..40666158,2	MCF-7	breast:
6	chr12:40616874..40619503-chr12:40632557..40634590,2	MCF-7	breast:
7	chr12:40546325..40546967-chr12:40662693..40663558,3	MCF-7	breast:
8	chr12:40615913..40618239-chr12:40619276..40621204,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000225342	TF binding region
ENSG00000225342	CpG island
ENSG00000143570	chromatin interactions
ENSG00000188906	chromatin interactions
ENSG00000225342	chromatin interactions
ENSG00000143578	chromatin interactions
ENSG00000205592	chromatin interactions

Extended variants
information (count: 1742 )
Associated
traits (count: 56 )

Variant overlapped rSNPs/rCNVs (count:1742 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs542882312	chr12:40620566-40620567	Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs141285803	chr12:40620577-40620578	Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs573289422	chr12:40620631-40620632	Flanking Active TSS Active TSS Enhancers Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs17443387	chr12:40620635-40620636	Flanking Active TSS Active TSS Enhancers Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs565293422	chr12:40620652-40620653	Flanking Active TSS Active TSS Enhancers Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs532403244	chr12:40620658-40620659	Flanking Active TSS Active TSS Enhancers Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs557112945	chr12:40620677-40620678	Flanking Active TSS Active TSS Enhancers Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs187204402	chr12:40620703-40620704	Flanking Active TSS Active TSS Enhancers Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs549268245	chr12:40620715-40620716	Flanking Active TSS Active TSS Enhancers Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs191238180	chr12:40620755-40620756	Flanking Active TSS Active TSS Enhancers Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs548386696	chr12:40620771-40620772	Flanking Active TSS Active TSS Enhancers Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs567205454	chr12:40620787-40620788	Flanking Active TSS Active TSS Enhancers Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs1491942	chr12:40620808-40620809	Flanking Active TSS Active TSS Enhancers Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance disease
14	rs1491941	chr12:40620815-40620816	Flanking Active TSS Active TSS Enhancers Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs571207568	chr12:40620847-40620848	Flanking Active TSS Active TSS Enhancers Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs538683367	chr12:40620865-40620866	Flanking Active TSS Active TSS Enhancers Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs17465751	chr12:40620881-40620882	Flanking Active TSS Active TSS Enhancers Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs548999464	chr12:40620882-40620883	Flanking Active TSS Active TSS Enhancers Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs150224676	chr12:40620886-40620887	Flanking Active TSS Active TSS Enhancers Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs183766741	chr12:40620917-40620918	Flanking Active TSS Active TSS Enhancers Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs562005359	chr12:40620963-40620964	Flanking Active TSS Active TSS Enhancers Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs529108864	chr12:40620966-40620967	Flanking Active TSS Active TSS Enhancers Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs573219333	chr12:40620970-40620971	Flanking Active TSS Active TSS Enhancers Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs138873140	chr12:40620978-40620979	Flanking Active TSS Active TSS Enhancers Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs565261463	chr12:40620988-40620989	Flanking Active TSS Active TSS Enhancers Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs79857753	chr12:40620995-40620996	Flanking Active TSS Active TSS Enhancers Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs372565188	chr12:40621029-40621030	Enhancers Active TSS Weak transcription Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs113137919	chr12:40621041-40621042	Enhancers Active TSS Weak transcription Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs550725200	chr12:40621101-40621102	Enhancers Active TSS Weak transcription Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs376348983	chr12:40621134-40621135	Enhancers Active TSS Weak transcription Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs149406366	chr12:40621156-40621157	Enhancers Active TSS Weak transcription Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs532826201	chr12:40621195-40621196	Enhancers Active TSS Weak transcription Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs562804552	chr12:40621218-40621219	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs373570858	chr12:40621254-40621255	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs76292542	chr12:40621287-40621288	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs187732324	chr12:40621329-40621330	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs35548649	chr12:40621358-40621359	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs560753045	chr12:40621396-40621397	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs143792605	chr12:40621428-40621429	Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs547362576	chr12:40621460-40621461	Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs193236193	chr12:40621473-40621474	Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs145334235	chr12:40621487-40621488	Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs571406587	chr12:40621582-40621583	Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs532104079	chr12:40621586-40621587	Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs138538499	chr12:40621589-40621590	Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs569145417	chr12:40621593-40621594	Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs536563723	chr12:40621605-40621606	Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs185655814	chr12:40621652-40621653	Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs144139456	chr12:40621653-40621654	Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs533791258	chr12:40621663-40621664	Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:56)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
Seminomas	18059402	CNVD
Wilms tumour	21544195	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
Ewing''s sarcoma	21437220	CNVD
Testicular germ cell tumor	18059402	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Ewing''s sarcoma	17952124	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Cancer	20164919	CNVD
Neurodevelopmental disorder	22521361	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Renal cell carcinoma	18194544	CNVD
Breast cancer	21949216	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21637783	CNVD
Glioblastoma multiforme	21080181	CNVD
Renal cell carcinoma	19461508	CNVD
Burkitt''s lymphoma	18698080	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	17603634	CNVD
Cancer	21183584	CNVD
Hirschsprung''s Disease	21712996	CNVD
Lissencephaly	21572526	CNVD
Lung cancer	18438408	CNVD
Acute myeloid leukemia	21251322	CNVD
small cell lung cancer	20016488	CNVD
Autism	20858243	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Breast cancer	19602461	CNVD
Breast cancer	17899364	CNVD
Cancer	20164920	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	21364760	CNVD

Chromatin state (count:457 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:40616000-40621200	Active TSS	Primary monocytes fromperipheralblood	blood
2	chr12:40616600-40621000	Active TSS	Duodenum Smooth Muscle	Duodenum
3	chr12:40616800-40620800	Active TSS	Primary mononuclear cells fromperipheralblood	Blood
4	chr12:40617000-40620600	Active TSS	Fetal Kidney	kidney
5	chr12:40617400-40620600	Active TSS	Stomach Smooth Muscle	stomach
6	chr12:40617400-40620800	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
7	chr12:40617400-40620800	Active TSS	Skeletal Muscle Male	skeletal muscle
8	chr12:40617400-40621000	Active TSS	Rectal Mucosa Donor 29	rectum
9	chr12:40617400-40621000	Active TSS	Right Atrium	heart
10	chr12:40617400-40621400	Active TSS	Aorta	Aorta
11	chr12:40617600-40620800	Active TSS	Brain Anterior Caudate	brain
12	chr12:40617800-40620800	Active TSS	Brain Hippocampus Middle	brain
13	chr12:40617800-40621000	Active TSS	Rectal Smooth Muscle	rectum
14	chr12:40618000-40620800	Active TSS	Lung	lung
15	chr12:40618000-40621000	Active TSS	A549	lung
16	chr12:40618200-40620600	Active TSS	Fetal Adrenal Gland	Adrenal Gland
17	chr12:40618200-40620800	Active TSS	Brain Inferior Temporal Lobe	brain
18	chr12:40618200-40620800	Active TSS	Rectal Mucosa Donor 31	rectum
19	chr12:40618800-40620800	Flanking Active TSS	GM12878-XiMat	blood
20	chr12:40618800-40621200	Flanking Active TSS	Primary B cells from cord blood	blood
21	chr12:40619000-40621000	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
22	chr12:40619000-40621000	Flanking Active TSS	Muscle Satellite Cultured Cells	--
23	chr12:40619200-40621200	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
24	chr12:40619400-40620800	Active TSS	Brain Cingulate Gyrus	brain
25	chr12:40619400-40620800	Active TSS	Duodenum Mucosa	Duodenum
26	chr12:40619400-40621000	Enhancers	HUVEC	blood vessel
27	chr12:40619400-40634600	Weak transcription	Spleen	Spleen
28	chr12:40619400-40644400	Weak transcription	Gastric	stomach
29	chr12:40619600-40620600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
30	chr12:40619600-40620600	Weak transcription	Esophagus	oesophagus
31	chr12:40619600-40620600	Weak transcription	Left Ventricle	heart
32	chr12:40619600-40620600	Weak transcription	Pancreas	Pancrea
33	chr12:40619600-40621000	Enhancers	HMEC	breast
34	chr12:40619600-40621000	Enhancers	NHEK	skin
35	chr12:40619600-40621000	Enhancers	Osteobl	bone
36	chr12:40619600-40636400	Weak transcription	Fetal Muscle Leg	muscle
37	chr12:40619600-40661000	Weak transcription	Sigmoid Colon	Sigmoid Colon
38	chr12:40619600-40678400	Weak transcription	Right Ventricle	heart
39	chr12:40619800-40620600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
40	chr12:40619800-40658800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
41	chr12:40620000-40620600	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
42	chr12:40620000-40620600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
43	chr12:40620000-40621000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
44	chr12:40620000-40621000	Enhancers	Pancreatic Islets	Pancreatic Islet
45	chr12:40620200-40620600	Active TSS	Adipose Nuclei	Adipose
46	chr12:40620200-40620800	Flanking Active TSS	Primary B cells from peripheral blood	blood
47	chr12:40620200-40620800	Enhancers	Stomach Mucosa	stomach
48	chr12:40620200-40620800	Enhancers	NH-A	brain
49	chr12:40620200-40621000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
50	chr12:40620200-40621000	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin

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