Variant report

Variant	esv3487503
Chromosome Location	chr12:65016285-65019683
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:388)
CpG islands
(count:61)
Chromatin interactive
region (count:26)
LncRNA
region (count:0)
Mature miRNA
region (count: 3)
miRNA target
sites (count:0)

(count:388 , 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	ARID3A	chr12:65018938-65019964	K562	blood:	n/a	n/a
2	ARID3A	chr12:65019023-65019740	HepG2	liver:	n/a	n/a
3	ATF1	chr12:65019032-65019882	K562	blood:	n/a	n/a
4	ATF2	chr12:65018973-65019973	GM12878	blood:	n/a	n/a
5	ATF2	chr12:65018928-65019993	GM12878	blood:	n/a	n/a
6	BATF	chr12:65019124-65019893	GM12878	blood:	n/a	n/a
7	BCL3	chr12:65018853-65019864	A549	lung:	n/a	chr12:65019643-65019652 chr12:65019642-65019651
8	BCL3	chr12:65018952-65019624	A549	lung:	n/a	n/a
9	BCLAF1	chr12:65018905-65019893	GM12878	blood:	n/a	chr12:65019643-65019652 chr12:65019642-65019651
10	BHLHE40	chr12:65019083-65019796	A549	lung:	n/a	chr12:65019469-65019485
11	BHLHE40	chr12:65019002-65019972	GM12878	blood:	n/a	chr12:65019469-65019485
12	BHLHE40	chr12:65017923-65017924	K562	blood:	n/a	n/a
13	BHLHE40	chr12:65018993-65019875	K562	blood:	n/a	chr12:65019469-65019485
14	BRCA1	chr12:65019057-65019823	Hela-S3	cervix:	n/a	n/a
15	CBX3	chr12:65019065-65019904	K562	blood:	n/a	n/a
16	CEBPB	chr12:65018929-65019751	Hela-S3	cervix:	n/a	n/a
17	CEBPB	chr12:65018854-65019638	MCF-7	breast:	n/a	chr12:65018912-65018920
18	CEBPB	chr12:65016332-65016456	A549	lung:	n/a	n/a
19	CEBPB	chr12:65018963-65019771	IMR90	lung:	n/a	n/a
20	CEBPB	chr12:65018878-65019786	MCF-7	breast:	n/a	chr12:65018912-65018920
21	CEBPB	chr12:65018845-65019794	A549	lung:	n/a	chr12:65018912-65018920
22	CEBPB	chr12:65018981-65019280	HepG2	liver:	n/a	n/a
23	CEBPB	chr12:65018876-65019346	A549	lung:	n/a	chr12:65018912-65018920
24	CEBPB	chr12:65016302-65016468	K562	blood:	n/a	n/a
25	CEBPB	chr12:65018912-65019489	K562	blood:	n/a	chr12:65018912-65018920
26	CEBPB	chr12:65018911-65020020	GM12878	blood:	n/a	chr12:65018912-65018920
27	CEBPB	chr12:65019012-65019271	K562	blood:	n/a	n/a
28	CEBPB	chr12:65018923-65019690	K562	blood:	n/a	n/a
29	CEBPB	chr12:65018949-65019713	A549	lung:	n/a	n/a
30	CHD1	chr12:65018855-65019940	GM12878	blood:	n/a	n/a
31	CHD2	chr12:65019460-65019653	HepG2	liver:	n/a	n/a
32	CHD2	chr12:65019179-65019737	Hela-S3	cervix:	n/a	n/a
33	CHD2	chr12:65019041-65019818	GM12878	blood:	n/a	n/a
34	CREB1	chr12:65018889-65019947	GM12878	blood:	n/a	n/a
35	CREB1	chr12:65019247-65019661	A549	lung:	n/a	n/a
36	CTCF	chr12:65019073-65019112	Pancreas_OC	pancreas:	n/a	n/a
37	CTCF	chr12:65019000-65019150	NB4	blood:	n/a	n/a
38	CTCF	chr12:65019028-65019172	HUVEC	blood vessel:	n/a	n/a
39	CTCF	chr12:65019070-65019120	K562	blood:	n/a	n/a
40	CTCF	chr12:65018980-65019130	HPAF	blood vessel:	n/a	n/a
41	CTCF	chr12:65018959-65019165	HepG2	liver:	n/a	n/a
42	CTCF	chr12:65019580-65019730	AG04449	skin:	n/a	n/a
43	CTCF	chr12:65018918-65019636	K562	blood:	n/a	n/a
44	CTCF	chr12:65019520-65019670	HCPEpiC	choroid plexus:	n/a	n/a
45	CTCF	chr12:65018511-65018560	ProgFib	skin:	n/a	n/a
46	CTCF	chr12:65019080-65019230	A549	lung:	n/a	n/a
47	CTCF	chr12:65019100-65019250	HVMF	connective:	n/a	n/a
48	CTCF	chr12:65018937-65019178	A549	lung:	n/a	n/a
49	CTCF	chr12:65018992-65019264	GM12878	blood:	n/a	n/a
50	CTCF	chr12:65019026-65019130	HepG2	liver:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:65019329-65019379	U87	brain:	n/a
2	chr12:65019329-65019379	GM12892	blood:	n/a
3	chr12:65019329-65019379	Jurkat	blood:	n/a
4	chr12:65019329-65019379	CMK	blood:	n/a
5	chr12:65019329-65019379	HUVEC	blood vessel:	n/a
6	chr12:65019329-65019379	HepG2	liver:	n/a
7	chr12:65019329-65019379	BE2_C	brain:	n/a
8	chr12:65019329-65019379	HCM	heart:	n/a
9	chr12:65019329-65019379	AG09309	skin:	n/a
10	chr12:65019329-65019379	AG04450	lung:	fetal
11	chr12:65019329-65019379	LNCaP	prostate:	n/a
12	chr12:65019329-65019379	HEK293	kidney:	embryo
13	chr12:65019329-65019379	GM12878	blood:	n/a
14	chr12:65019329-65019379	SK-N-MC	brain:	n/a
15	chr12:65019329-65019379	HPAEpiC	pulmonary alveolar:	n/a
16	chr12:65019329-65019379	Caco-2	colon:	n/a
17	chr12:65019329-65019379	BJ	skin:	n/a
18	chr12:65019329-65019379	GM12891	blood:	n/a
19	chr12:65019329-65019379	NHBE	bronchial:	n/a
20	chr12:65019329-65019379	HL-60	blood:	n/a
21	chr12:65019329-65019379	IMR90	lung:	fetal
22	chr12:65019329-65019379	SAEC	small airway:	n/a
23	chr12:65019329-65019379	GM19239	blood:	n/a
24	chr12:65019329-65019379	SKMC	muscle:	n/a
25	chr12:65019329-65019379	GM06990	blood:	n/a
26	chr12:65019329-65019379	AG09319	gingival:	n/a
27	chr12:65019329-65019379	ovcar-3	ovarian:	n/a
28	chr12:65019329-65019379	ProgFib	skin:	n/a
29	chr12:65019329-65019379	HRE	kidney:	n/a
30	chr12:65019329-65019379	HIPEpiC	eye:	n/a
31	chr12:65019329-65019379	AG04449	skin:	fetal
32	chr12:65019329-65019379	HCF	heart:	n/a
33	chr12:65019329-65019379	HRPEpiC	eye:	n/a
34	chr12:65019329-65019379	RPTEC	kidney:	n/a
35	chr12:65019329-65019379	SK-N-SH_RA	brain:	n/a
36	chr12:65019329-65019379	HEEpiC	esophagus:	n/a
37	chr12:65019329-65019379	HNPCEpiC	eye:	n/a
38	chr12:65019329-65019379	NH-A	brain:	n/a
39	chr12:65019329-65019379	NB4	blood:	n/a
40	chr12:65019329-65019379	PFSK-1	brain:	n/a
41	chr12:65019329-65019379	MCF-7	breast:	n/a
42	chr12:65019329-65019379	SK-N-SH	brain:	n/a
43	chr12:65019329-65019379	NT2-D1	testis:	n/a
44	chr12:65019329-65019379	H1-hESC	embryonic stem cell:	embryo
45	chr12:65019329-65019379	Hela-S3	cervix:	n/a
46	chr12:65019329-65019379	HRCEpiC	kidney:	n/a
47	chr12:65019329-65019379	HCPEpiC	choroid plexus:	n/a
48	chr12:65019329-65019379	AG10803	skin:	n/a
49	chr12:65019329-65019379	PrEC	prostate:	n/a
50	chr12:65019329-65019379	HMEC	breast:	n/a

(count:26 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:65019263..65021039-chr12:65064985..65067371,4	MCF-7	breast:
2	chr12:65001678..65008078-chr12:65013108..65023657,17	MCF-7	breast:
3	chr12:65010556..65012937-chr12:65017376..65021348,4	K562	blood:
4	chr12:65018061..65020835-chr12:65174615..65176151,2	MCF-7	breast:
5	chr12:65004562..65005411-chr12:65018842..65019420,4	MCF-7	breast:
6	chr12:65014921..65016651-chr12:65088874..65091449,2	MCF-7	breast:
7	chr12:65008925..65011325-chr12:65018761..65021697,3	MCF-7	breast:
8	chr12:65019590..65021389-chr12:65024467..65026055,3	K562	blood:
9	chr12:65001526..65007900-chr12:65015799..65021807,8	K562	blood:
10	chr12:65018082..65020499-chr12:65056309..65058062,2	MCF-7	breast:
11	chr12:64989403..64992125-chr12:65016566..65018354,2	MCF-7	breast:
12	chr12:65004562..65005438-chr12:65018842..65019420,5	MCF-7	breast:
13	chr12:65016442..65019284-chr12:65019658..65023232,4	MCF-7	breast:
14	chr12:65017129..65019171-chr12:65067339..65069384,2	MCF-7	breast:
15	chr12:65018029..65021346-chr12:65072247..65076410,6	MCF-7	breast:
16	chr12:65019301..65021176-chr12:65062867..65064609,2	K562	blood:
17	chr12:65017089..65019712-chr12:65042869..65045588,2	MCF-7	breast:
18	chr12:65008839..65011429-chr12:65017334..65019705,2	MCF-7	breast:
19	chr12:64844472..64846840-chr12:65019435..65021283,2	MCF-7	breast:
20	chr12:65018895..65020884-chr12:65086015..65088325,2	MCF-7	breast:
21	chr12:65013677..65016643-chr12:65019438..65021046,2	K562	blood:
22	chr12:65011462..65014885-chr12:65017332..65020916,6	MCF-7	breast:
23	chr12:65019020..65021619-chr12:65065192..65067422,3	MCF-7	breast:
24	chr12:65018258..65020873-chr12:65068837..65071390,2	MCF-7	breast:
25	chr12:65013056..65015741-chr12:65019440..65021647,2	MCF-7	breast:
26	chr12:65013129..65015693-chr12:65017473..65019068,2	K562	blood:

No data

miRNA name	Chromosome Location	mirBase accession
hsa-miR-548z	chr12:65016310-65016332	MIMAT0018446
hsa-miR-548c-5p	chr12:65016313-65016334	MIMAT0004806
hsa-miR-548c-3p	chr12:65016349-65016370	MIMAT0003285

No data

Variant related genes	Relation type
MIR548C	TF binding region
ENSG00000225195	TF binding region
MIR548C	CpG island
ENSG00000225195	CpG island
ENSG00000207546	chromatin interactions
ENSG00000256670	chromatin interactions
ENSG00000111490	chromatin interactions
ENSG00000268028	chromatin interactions
ENSG00000153179	chromatin interactions
ENSG00000225195	chromatin interactions
ENSG00000183735	chromatin interactions

Extended variants
information (count: 134 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:134 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17120527	chr12:65016300-65016301	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs374151873	chr12:65016320-65016321	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region miRNA	3 gene(s)	Overlapped CNVs	n/a
3	rs540698062	chr12:65016325-65016326	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region miRNA	3 gene(s)	Overlapped CNVs	n/a
4	rs199967481	chr12:65016391-65016392	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs368872280	chr12:65016416-65016417	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs531509073	chr12:65016474-65016475	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs375333471	chr12:65016489-65016490	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs191559010	chr12:65016544-65016545	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs573959618	chr12:65016545-65016546	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs78458236	chr12:65016585-65016586	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs542988090	chr12:65016635-65016636	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs563189811	chr12:65016714-65016715	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs184866777	chr12:65016728-65016729	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs545203919	chr12:65016761-65016762	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs565100870	chr12:65016773-65016774	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs542383645	chr12:65016802-65016803	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs559149740	chr12:65016807-65016808	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs547065310	chr12:65016821-65016822	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs567184803	chr12:65016827-65016828	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs529682204	chr12:65016844-65016845	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs549852562	chr12:65016852-65016853	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs189626522	chr12:65016864-65016865	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs538895664	chr12:65016890-65016891	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs558802455	chr12:65016892-65016893	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs565852069	chr12:65016903-65016904	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs534316838	chr12:65016905-65016906	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs376621256	chr12:65016940-65016941	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs182400692	chr12:65016978-65016979	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs531274370	chr12:65017022-65017023	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs1245170	chr12:65017086-65017087	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs144269017	chr12:65017144-65017145	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs147829374	chr12:65017148-65017149	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs576341661	chr12:65017177-65017178	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs545265307	chr12:65017192-65017193	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs141285729	chr12:65017198-65017199	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs373412364	chr12:65017293-65017294	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs553056057	chr12:65017341-65017342	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs561034841	chr12:65017369-65017370	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs59219879	chr12:65017484-65017485	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs56185632	chr12:65017491-65017492	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs60649666	chr12:65017502-65017503	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs549760714	chr12:65017503-65017504	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs563241924	chr12:65017504-65017505	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs532470335	chr12:65017505-65017506	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs57471087	chr12:65017506-65017507	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs552478010	chr12:65017518-65017519	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs58422857	chr12:65017543-65017544	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs55923537	chr12:65017586-65017587	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs55905863	chr12:65017595-65017596	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs55663246	chr12:65017601-65017602	Enhancers Weak transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:83)

Disease	PMID	Source
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
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	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
Lissencephaly	21572526	CNVD
Lung cancer	18438408	CNVD
Breast cancer	17899364	CNVD
Colorectal cancer	16272173	CNVD
Glioblastoma multiforme	17387387	CNVD
liposarcomas	17372913	CNVD
Non-small cell lung cancer	24170126	CNVD
Cancer	16751803	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	21785460	CNVD
small cell lung cancer	20016488	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	21390271	CNVD
Cancer	20164919	CNVD
Leukemia	18628472	CNVD
Phyllodes tumor	17334353	CNVD
Glaucoma	21310917	CNVD
Breast cancer	16272173	CNVD
Mental retardation	19951919	CNVD
Glaucoma	21447600	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Developmental delay	21267005	CNVD
12q14 microdeletion syndrome	21267005	CNVD
Developmental delay	19277063	CNVD
Dwarfism	19277063	CNVD
Fibroblasts	20926602	CNVD
Metanephric adenoma	20802469	CNVD
Follicular lymphoma	18703704	CNVD
Acute myeloid leukemia	21251322	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Multiple myeloma	16616336	CNVD
Lung cancer	16773561	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Mental retardation	17220210	CNVD
Osteopoikilosis	17220210	CNVD
short stature	17220210	CNVD
Burkitt''s lymphoma	20823134	CNVD
abnormal development	18461090	CNVD
Prostate cancer	18632612	CNVD
Myelofibrosis	22110671	CNVD
Heart disease	21282601	CNVD
Ovarian neoplasms	16753589	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	16620391	CNVD
Intracranial arachnoid cysts	20187927	CNVD
Melanoma	20877625	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:374 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:65005800-65017800	Weak transcription	Gastric	stomach
2	chr12:65006200-65017400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
3	chr12:65006200-65017600	Weak transcription	H1 Cell Line	embryonic stem cell
4	chr12:65006200-65018800	Weak transcription	Fetal Thymus	thymus
5	chr12:65006200-65019000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
6	chr12:65006200-65019000	Weak transcription	NHEK	skin
7	chr12:65006200-65019400	Weak transcription	Psoas Muscle	Psoas
8	chr12:65006400-65017000	Weak transcription	HUES6 Cell Line	embryonic stem cell
9	chr12:65006600-65017400	Weak transcription	Small Intestine	intestine
10	chr12:65006600-65018200	Weak transcription	Fetal Intestine Large	intestine
11	chr12:65006800-65031800	Weak transcription	Dnd41	blood
12	chr12:65007000-65018800	Weak transcription	HMEC	breast
13	chr12:65007000-65019200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
14	chr12:65007200-65017600	Weak transcription	Stomach Mucosa	stomach
15	chr12:65007800-65017600	Weak transcription	Lung	lung
16	chr12:65008600-65019000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
17	chr12:65009200-65019200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
18	chr12:65009800-65019200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
19	chr12:65009800-65019400	Weak transcription	Fetal Muscle Trunk	muscle
20	chr12:65010000-65023200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
21	chr12:65010200-65019400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr12:65010400-65017000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
23	chr12:65010400-65017000	Weak transcription	NH-A	brain
24	chr12:65010400-65018200	Weak transcription	Colonic Mucosa	Colon
25	chr12:65010400-65019000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
26	chr12:65010600-65017800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
27	chr12:65010600-65018800	Weak transcription	Cortex derived primary cultured neurospheres	brain
28	chr12:65010600-65018800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
29	chr12:65010600-65018800	Weak transcription	Fetal Lung	lung
30	chr12:65010600-65019000	Weak transcription	Fetal Stomach	stomach
31	chr12:65010800-65018600	Weak transcription	Fetal Muscle Leg	muscle
32	chr12:65010800-65022200	Weak transcription	Spleen	Spleen
33	chr12:65011000-65018400	Weak transcription	Brain Substantia Nigra	brain
34	chr12:65011200-65018800	Enhancers	Primary B cells from peripheral blood	blood
35	chr12:65011600-65019000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
36	chr12:65011800-65019000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
37	chr12:65012000-65016600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
38	chr12:65012000-65017600	Weak transcription	Duodenum Smooth Muscle	Duodenum
39	chr12:65012400-65018200	Weak transcription	Fetal Intestine Small	intestine
40	chr12:65012400-65019200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
41	chr12:65012600-65019200	Enhancers	Primary T helper naive cells from peripheral blood	blood
42	chr12:65012800-65017000	Enhancers	A549	lung
43	chr12:65013000-65019200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
44	chr12:65013200-65016600	Weak transcription	Aorta	Aorta
45	chr12:65013200-65019000	Weak transcription	Right Ventricle	heart
46	chr12:65013200-65019200	Weak transcription	Brain Anterior Caudate	brain
47	chr12:65013200-65019400	Weak transcription	Esophagus	oesophagus
48	chr12:65013200-65019400	Weak transcription	Ovary	ovary
49	chr12:65013400-65017000	Weak transcription	HUES48 Cell Line	embryonic stem cell
50	chr12:65013400-65017000	Weak transcription	Muscle Satellite Cultured Cells	--

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