Variant report

Variant	nsv976612
Chromosome Location	chr12:49666119-49668483
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:264)
CpG islands
(count:61)
Chromatin interactive
region (count:20)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:264 , 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	chr12:49667397-49667437	K562	blood:	n/a	n/a
2	ATF2	chr12:49667448-49667725	H1-hESC	embryonic stem cell:	n/a	n/a
3	BCL3	chr12:49667126-49668034	K562	blood:	n/a	n/a
4	BCL3	chr12:49667090-49669237	A549	lung:	n/a	n/a
5	BCL3	chr12:49668330-49668665	K562	blood:	n/a	n/a
6	BCL3	chr12:49666451-49668725	K562	blood:	n/a	n/a
7	BCL3	chr12:49667012-49669173	A549	lung:	n/a	n/a
8	BCLAF1	chr12:49668198-49668515	GM12878	blood:	n/a	n/a
9	BCLAF1	chr12:49668225-49668609	K562	blood:	n/a	n/a
10	BCLAF1	chr12:49666855-49668146	K562	blood:	n/a	n/a
11	BCLAF1	chr12:49666390-49668252	K562	blood:	n/a	n/a
12	BHLHE40	chr12:49667533-49667853	K562	blood:	n/a	n/a
13	CBX3	chr12:49666558-49667794	K562	blood:	n/a	n/a
14	CCNT2	chr12:49667398-49667946	K562	blood:	n/a	n/a
15	CEBPB	chr12:49665827-49666141	A549	lung:	n/a	n/a
16	CEBPB	chr12:49667645-49667920	K562	blood:	n/a	n/a
17	CEBPB	chr12:49665927-49666145	IMR90	lung:	n/a	n/a
18	CEBPB	chr12:49665831-49666141	K562	blood:	n/a	n/a
19	CEBPB	chr12:49665877-49666157	HepG2	liver:	n/a	n/a
20	CEBPD	chr12:49666588-49668117	K562	blood:	n/a	n/a
21	CHD2	chr12:49667123-49668835	K562	blood:	n/a	n/a
22	CREB1	chr12:49667152-49667666	K562	blood:	n/a	n/a
23	CREB1	chr12:49667583-49668069	A549	lung:	n/a	n/a
24	CTCF	chr12:49667440-49667590	HEK293	kidney:	n/a	n/a
25	CTCF	chr12:49666523-49666622	LNCaP	prostate:	n/a	n/a
26	CTCF	chr12:49667720-49667870	Hela-S3	cervix:	n/a	n/a
27	CTCF	chr12:49667720-49667870	HepG2	liver:	n/a	n/a
28	CTCF	chr12:49666560-49666660	LNCaP	prostate:	n/a	n/a
29	CTCF	chr12:49666440-49667073	T-47D	breast:	n/a	n/a
30	EBF1	chr12:49666480-49666828	GM12878	blood:	n/a	n/a
31	EGR1	chr12:49666968-49667866	K562	blood:	n/a	n/a
32	ELF1	chr12:49667095-49667468	K562	blood:	n/a	n/a
33	ELF1	chr12:49668172-49668618	A549	lung:	n/a	n/a
34	EP300	chr12:49666474-49667115	T-47D	breast:	n/a	n/a
35	EP300	chr12:49666050-49666772	GM12878	blood:	n/a	n/a
36	ETS1	chr12:49668110-49668657	A549	lung:	n/a	n/a
37	FOS	chr12:49668301-49668501	MCF10A-Er-Src	breast:	n/a	n/a
38	FOSL2	chr12:49666754-49666993	HepG2	liver:	n/a	n/a
39	GATA2	chr12:49666030-49667458	K562	blood:	n/a	chr12:49667123-49667130
40	GATA3	chr12:49667335-49668769	A549	lung:	n/a	n/a
41	GTF2F1	chr12:49668440-49668714	K562	blood:	n/a	n/a
42	HCFC1	chr12:49667253-49667302	K562	blood:	n/a	n/a
43	HEY1	chr12:49664685-49668312	K562	blood:	n/a	n/a
44	HEY1	chr12:49668033-49668377	HepG2	liver:	n/a	n/a
45	HEY1	chr12:49666147-49666645	HepG2	liver:	n/a	n/a
46	HEY1	chr12:49666035-49667525	HepG2	liver:	n/a	n/a
47	HEY1	chr12:49665972-49668094	K562	blood:	n/a	n/a
48	HEY1	chr12:49667070-49667648	HepG2	liver:	n/a	n/a
49	HEY1	chr12:49666691-49667014	HepG2	liver:	n/a	n/a
50	HEY1	chr12:49667663-49668045	HepG2	liver:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:49667081-49667131	NH-A	brain:	n/a
2	chr12:49667081-49667131	GM19239	blood:	n/a
3	chr12:49667081-49667131	HCPEpiC	choroid plexus:	n/a
4	chr12:49667081-49667131	GM12878	blood:	n/a
5	chr12:49667081-49667131	SK-N-SH	brain:	n/a
6	chr12:49667081-49667131	AG10803	skin:	n/a
7	chr12:49667081-49667131	HEEpiC	esophagus:	n/a
8	chr12:49667081-49667131	SAEC	small airway:	n/a
9	chr12:49667081-49667131	A549	lung:	n/a
10	chr12:49667081-49667131	HMEC	breast:	n/a
11	chr12:49667081-49667131	SK-N-SH_RA	brain:	n/a
12	chr12:49667081-49667131	HRPEpiC	eye:	n/a
13	chr12:49667081-49667131	AG04450	lung:	fetal
14	chr12:49667081-49667131	HRCEpiC	kidney:	n/a
15	chr12:49667081-49667131	MCF10A-Er-Src	breast:	n/a
16	chr12:49667081-49667131	AG04449	skin:	fetal
17	chr12:49667081-49667131	HCT-116	colon:	n/a
18	chr12:49667081-49667131	Caco-2	colon:	n/a
19	chr12:49667081-49667131	AoSMC	blood vessel:	n/a
20	chr12:49667081-49667131	HUVEC	blood vessel:	n/a
21	chr12:49667081-49667131	SK-N-MC	brain:	n/a
22	chr12:49667081-49667131	HRE	kidney:	n/a
23	chr12:49667081-49667131	Hepatocyte	liver:	n/a
24	chr12:49667081-49667131	RPTEC	kidney:	n/a
25	chr12:49667081-49667131	NHBE	bronchial:	n/a
26	chr12:49667081-49667131	ECC-1	luminal epithelium:	n/a
27	chr12:49667081-49667131	Jurkat	blood:	n/a
28	chr12:49667081-49667131	U87	brain:	n/a
29	chr12:49667081-49667131	AG09309	skin:	n/a
30	chr12:49667081-49667131	PANC-1	pancreas:	n/a
31	chr12:49667081-49667131	NT2-D1	testis:	n/a
32	chr12:49667081-49667131	LNCaP	prostate:	n/a
33	chr12:49667081-49667131	HepG2	liver:	n/a
34	chr12:49667081-49667131	NHDF-neo	bronchial:	n/a
35	chr12:49667081-49667131	BJ	skin:	n/a
36	chr12:49667081-49667131	ProgFib	skin:	n/a
37	chr12:49667081-49667131	SKMC	muscle:	n/a
38	chr12:49667081-49667131	IMR90	lung:	fetal
39	chr12:49667081-49667131	MCF-7	breast:	n/a
40	chr12:49667081-49667131	HIPEpiC	eye:	n/a
41	chr12:49667081-49667131	CMK	blood:	n/a
42	chr12:49667081-49667131	H1-hESC	embryonic stem cell:	embryo
43	chr12:49667081-49667131	BE2_C	brain:	n/a
44	chr12:49667081-49667131	AG09319	gingival:	n/a
45	chr12:49667081-49667131	PrEC	prostate:	n/a
46	chr12:49667081-49667131	NB4	blood:	n/a
47	chr12:49667081-49667131	HEK293	kidney:	embryo
48	chr12:49667081-49667131	HCM	heart:	n/a
49	chr12:49667081-49667131	T-47D	breast:	n/a
50	chr12:49667081-49667131	HL-60	blood:	n/a

(count:20 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:49523127..49526155-chr12:49667398..49671055,3	K562	blood:
2	chr12:49523333..49525156-chr12:49664494..49666350,2	MCF-7	breast:
3	chr12:49523250..49526538-chr12:49663846..49666716,3	K562	blood:
4	chr12:49667022..49671096-chr12:49685141..49687523,3	K562	blood:
5	chr12:49462240..49465825-chr12:49663317..49667869,4	K562	blood:
6	chr12:49666275..49670972-chr12:49688443..49691988,7	K562	blood:
7	chr12:49628615..49630966-chr12:49665293..49667047,2	K562	blood:
8	chr12:49453019..49455407-chr12:49664114..49666981,2	K562	blood:
9	chr12:49667022..49669779-chr12:49685141..49687257,2	K562	blood:
10	chr12:49664091..49667882-chr12:49690109..49694759,4	K562	blood:
11	chr12:49667402..49669417-chr12:49680548..49682820,2	K562	blood:
12	chr12:49449335..49458365-chr12:49656751..49666981,25	K562	blood:
13	chr12:49667913..49670211-chr12:49679594..49681611,2	MCF-7	breast:
14	chr12:49667825..49672911-chr12:49731373..49736764,7	K562	blood:
15	chr12:49410579..49413468-chr12:49666098..49668038,2	K562	blood:
16	chr12:49668368..49669871-chr12:49682424..49685316,2	MCF-7	breast:
17	chr12:49665854..49668915-chr12:49685671..49689413,3	MCF-7	breast:
18	chr12:49666353..49668796-chr19:796925..798586,2	K562	blood:
19	chr12:49663971..49666837-chr12:49712458..49715347,2	K562	blood:
20	chr12:49667042..49668619-chr12:49959885..49961439,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000258232	TF binding region
ENSG00000258232	CpG island
ENSG00000258017	chromatin interactions
ENSG00000167550	chromatin interactions
ENSG00000123416	chromatin interactions
ENSG00000167548	chromatin interactions
ENSG00000187778	chromatin interactions
ENSG00000011304	chromatin interactions
ENSG00000135406	chromatin interactions
ENSG00000181929	chromatin interactions

Extended variants
information (count: 108 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:108 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs192154754	chr12:49666139-49666140	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
2	rs369308226	chr12:49666144-49666145	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
3	rs199599214	chr12:49666152-49666153	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
4	rs113331886	chr12:49666170-49666171	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
5	rs559395061	chr12:49666176-49666177	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
6	rs528051136	chr12:49666179-49666180	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
7	rs1057748	chr12:49666182-49666183	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
8	rs11542119	chr12:49666184-49666185	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
9	rs565412741	chr12:49666289-49666290	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
10	rs376776166	chr12:49666294-49666295	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
11	rs371063872	chr12:49666301-49666302	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
12	rs372926418	chr12:49666313-49666314	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
13	rs375933607	chr12:49666317-49666318	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
14	rs370276397	chr12:49666321-49666322	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
15	rs561090052	chr12:49666323-49666324	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
16	rs373730264	chr12:49666354-49666355	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
17	rs140286355	chr12:49666413-49666414	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
18	rs200651108	chr12:49666446-49666447	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
19	rs201965403	chr12:49666458-49666459	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
20	rs7974831	chr12:49666509-49666510	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs201310100	chr12:49666519-49666520	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
22	rs372810412	chr12:49666548-49666549	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
23	rs538625739	chr12:49666614-49666615	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
24	rs377596043	chr12:49666626-49666627	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
25	rs551680115	chr12:49666646-49666647	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
26	rs200317762	chr12:49666652-49666653	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
27	rs571434095	chr12:49666676-49666677	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
28	rs537291300	chr12:49666677-49666678	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
29	rs557189826	chr12:49666679-49666680	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
30	rs573833092	chr12:49666684-49666685	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
31	rs144002178	chr12:49666728-49666729	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
32	rs536362581	chr12:49666752-49666753	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
33	rs140582697	chr12:49666755-49666756	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
34	rs146417733	chr12:49666756-49666757	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
35	rs140667726	chr12:49666800-49666801	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
36	rs11542113	chr12:49666802-49666803	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
37	rs544657963	chr12:49666810-49666811	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
38	rs11542115	chr12:49666815-49666816	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs368180124	chr12:49666828-49666829	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
40	rs138174052	chr12:49666860-49666861	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
41	rs201921449	chr12:49666863-49666864	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
42	rs188605921	chr12:49666908-49666909	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
43	rs377694330	chr12:49666916-49666917	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
44	rs372085305	chr12:49666929-49666930	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
45	rs149194844	chr12:49666933-49666934	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
46	rs546709255	chr12:49666944-49666945	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
47	rs371067017	chr12:49666995-49666996	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs11542114	chr12:49667020-49667021	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs201038906	chr12:49667021-49667022	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs376096817	chr12:49667030-49667031	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:70)

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
Neurodevelopmental disorder	22521361	CNVD
T-cell prolymphocytic leukemia	19278963	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
Hirschsprung''s Disease	21712996	CNVD
Lissencephaly	21572526	CNVD
Lung cancer	18438408	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Breast cancer	19602461	CNVD
Breast cancer	17899364	CNVD
Colorectal cancer	16272173	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Adenoid cystic carcinoma	18332873	CNVD
Breast cancer	21364760	CNVD
Prostate cancer	18632612	CNVD
Follicular lymphoma	20505157	CNVD
Hepatocellular carcinoma	16750200	CNVD
Melanoma	18172304	CNVD
Metanephric adenoma	20802469	CNVD
Glioblastoma multiforme	17387387	CNVD
liposarcomas	17372913	CNVD
Non-small cell lung cancer	24170126	CNVD
Cancer	16751803	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Bladder cancer	21909424	CNVD
Multiple myeloma	16616336	CNVD
Intracranial aneurysm	16715129	CNVD
Breast cancer	17661082	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	21785460	CNVD
small cell lung cancer	20016488	CNVD
Myelofibrosis	22110671	CNVD
Intracranial ependymoma	16609018	CNVD
Cancer	17160897	CNVD
Cancer	20164919	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:213 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:49659200-49673600	Weak transcription	Fetal Brain Male	brain
2	chr12:49659600-49668600	Weak transcription	Brain Cingulate Gyrus	brain
3	chr12:49659600-49669600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
4	chr12:49659600-49673600	Weak transcription	Brain Hippocampus Middle	brain
5	chr12:49659800-49668600	Weak transcription	Right Atrium	heart
6	chr12:49661000-49668000	Strong transcription	H9 Cell Line	embryonic stem cell
7	chr12:49661000-49669800	Strong transcription	Fetal Stomach	stomach
8	chr12:49661600-49667400	Weak transcription	Fetal Heart	heart
9	chr12:49661600-49668000	Strong transcription	Fetal Thymus	thymus
10	chr12:49661600-49670600	Weak transcription	Psoas Muscle	Psoas
11	chr12:49661800-49668000	Strong transcription	HUES6 Cell Line	embryonic stem cell
12	chr12:49662000-49666400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr12:49662000-49667800	Strong transcription	iPS-18 Cell Line	embryonic stem cell
14	chr12:49662000-49667800	Strong transcription	Dnd41	blood
15	chr12:49662000-49668000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
16	chr12:49662000-49668600	Strong transcription	Primary hematopoietic stem cells short term culture	blood
17	chr12:49662200-49668600	Strong transcription	Primary T cells from cord blood	blood
18	chr12:49662600-49668000	Genic enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
19	chr12:49662600-49668400	Strong transcription	Rectal Mucosa Donor 29	rectum
20	chr12:49662600-49669000	Strong transcription	Fetal Muscle Leg	muscle
21	chr12:49662800-49667200	Strong transcription	iPS-15b Cell Line	embryonic stem cell
22	chr12:49662800-49667400	Strong transcription	GM12878-XiMat	blood
23	chr12:49662800-49667800	Strong transcription	HUES64 Cell Line	embryonic stem cell
24	chr12:49662800-49667800	Strong transcription	iPS-20b Cell Line	embryonic stem cell
25	chr12:49662800-49667800	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
26	chr12:49662800-49673400	Weak transcription	Brain Anterior Caudate	brain
27	chr12:49662800-49673400	Weak transcription	Brain Inferior Temporal Lobe	brain
28	chr12:49662800-49673400	Weak transcription	Brain Substantia Nigra	brain
29	chr12:49663000-49667400	Strong transcription	HepG2	liver
30	chr12:49663000-49667800	Strong transcription	HUES48 Cell Line	embryonic stem cell
31	chr12:49663000-49668000	Strong transcription	H1 Cell Line	embryonic stem cell
32	chr12:49663000-49668000	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
33	chr12:49663000-49668200	Strong transcription	Fetal Muscle Trunk	muscle
34	chr12:49663000-49668400	Strong transcription	Sigmoid Colon	Sigmoid Colon
35	chr12:49663000-49669600	Strong transcription	Thymus	Thymus
36	chr12:49663000-49669800	Strong transcription	Fetal Intestine Small	intestine
37	chr12:49663200-49667400	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
38	chr12:49663200-49667400	Strong transcription	Pancreas	Pancrea
39	chr12:49663200-49667800	Strong transcription	iPS DF 6.9 Cell Line	embryonic stem cell
40	chr12:49663200-49667800	Strong transcription	Primary T helper cells PMA-I stimulated	--
41	chr12:49663200-49667800	Strong transcription	Primary T helper cells fromperipheralblood	blood
42	chr12:49663200-49667800	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
43	chr12:49663200-49668000	Strong transcription	Adipose Nuclei	Adipose
44	chr12:49663200-49668000	Strong transcription	Colonic Mucosa	Colon
45	chr12:49663200-49668000	Strong transcription	Placenta	Placenta
46	chr12:49663200-49668200	Strong transcription	Lung	lung
47	chr12:49663200-49668600	Strong transcription	Primary neutrophils fromperipheralblood	blood
48	chr12:49663200-49668600	Strong transcription	Monocytes-CD14+_RO01746	blood
49	chr12:49663200-49669000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
50	chr12:49663200-49669200	Strong transcription	Duodenum Mucosa	Duodenum

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