Variant report

Variant	esv3378083
Chromosome Location	chr12:104530222-104533220
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:711)
CpG islands
(count:490)
Chromatin interactive
region (count:37)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:711 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:104531844-104532097	HepG2	liver:	n/a	n/a
2	ATF2	chr12:104531677-104532104	GM12878	blood:	n/a	n/a
3	ATF2	chr12:104531766-104532062	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF3	chr12:104531777-104532351	A549	lung:	n/a	n/a
5	BACH1	chr12:104531077-104531218	H1-hESC	embryonic stem cell:	n/a	n/a
6	BATF	chr12:104531839-104532100	GM12878	blood:	n/a	n/a
7	BCL3	chr12:104531716-104532463	A549	lung:	n/a	chr12:104532036-104532045 chr12:104532401-104532410 chr12:104532174-104532183
8	BCLAF1	chr12:104531764-104532118	GM12878	blood:	n/a	chr12:104532036-104532045
9	BCLAF1	chr12:104530703-104531373	GM12878	blood:	n/a	n/a
10	BCLAF1	chr12:104531731-104532209	GM12878	blood:	n/a	chr12:104532036-104532045 chr12:104532174-104532183
11	BHLHE40	chr12:104531679-104532329	HepG2	liver:	n/a	n/a
12	BHLHE40	chr12:104531274-104531321	GM12878	blood:	n/a	n/a
13	BHLHE40	chr12:104531812-104532099	GM12878	blood:	n/a	n/a
14	BHLHE40	chr12:104531797-104532337	K562	blood:	n/a	n/a
15	BRCA1	chr12:104531880-104532070	Hela-S3	cervix:	n/a	n/a
16	BRCA1	chr12:104532312-104532329	Hela-S3	cervix:	n/a	n/a
17	BRCA1	chr12:104532027-104532072	GM12878	blood:	n/a	n/a
18	BRCA1	chr12:104531864-104532064	H1-hESC	embryonic stem cell:	n/a	n/a
19	BRCA1	chr12:104532366-104532463	HepG2	liver:	n/a	n/a
20	CBX3	chr12:104532099-104532313	K562	blood:	n/a	n/a
21	CBX3	chr12:104531739-104532735	K562	blood:	n/a	n/a
22	CBX3	chr12:104531726-104532544	HCT-116	colon:	n/a	n/a
23	CCNT2	chr12:104531162-104532555	K562	blood:	n/a	chr12:104531268-104531277
24	CEBPB	chr12:104531828-104532155	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr12:104531877-104532046	H1-hESC	embryonic stem cell:	n/a	n/a
26	CEBPD	chr12:104531596-104531953	HepG2	liver:	n/a	n/a
27	CEBPD	chr12:104531053-104531540	HepG2	liver:	n/a	n/a
28	CEBPD	chr12:104531997-104532367	HepG2	liver:	n/a	n/a
29	CHD1	chr12:104530515-104531269	H1-hESC	embryonic stem cell:	n/a	n/a
30	CHD1	chr12:104531530-104531992	H1-hESC	embryonic stem cell:	n/a	n/a
31	CHD1	chr12:104530868-104532056	GM12878	blood:	n/a	n/a
32	CHD2	chr12:104531722-104532380	Hela-S3	cervix:	n/a	n/a
33	CHD2	chr12:104531768-104532683	K562	blood:	n/a	n/a
34	CHD2	chr12:104531776-104532367	H1-hESC	embryonic stem cell:	n/a	n/a
35	CHD2	chr12:104531781-104532351	GM12878	blood:	n/a	n/a
36	CHD2	chr12:104531788-104532527	HepG2	liver:	n/a	n/a
37	CHD2	chr12:104531081-104531332	GM12878	blood:	n/a	n/a
38	CREB1	chr12:104531728-104532290	HepG2	liver:	n/a	n/a
39	CREB1	chr12:104531774-104532259	H1-hESC	embryonic stem cell:	n/a	n/a
40	CREB1	chr12:104531738-104532379	K562	blood:	n/a	n/a
41	CREB1	chr12:104531546-104532447	HepG2	liver:	n/a	n/a
42	CREB1	chr12:104531748-104532073	A549	lung:	n/a	n/a
43	CREB1	chr12:104531759-104532301	GM12878	blood:	n/a	n/a
44	CREB1	chr12:104531062-104532428	A549	lung:	n/a	n/a
45	CTCF	chr12:104532200-104532350	HMEC	breast:	n/a	n/a
46	CTCF	chr12:104532420-104532570	HRPEpiC	eye:	n/a	n/a
47	CTCF	chr12:104531060-104531210	HMF	breast:	n/a	chr12:104531180-104531201
48	CTCF	chr12:104531156-104531238	MCF-7	breast:	n/a	chr12:104531180-104531201
49	CTCF	chr12:104531040-104531190	HBMEC	blood vessel:	n/a	n/a
50	CTCF	chr12:104532220-104532370	HCM	heart:	n/a	n/a

(count:490 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:104532011-104532061	HRPEpiC	eye:	n/a
2	chr12:104530941-104530991	T-47D	breast:	n/a
3	chr12:104532011-104532061	HRPEpiC	eye:	n/a
4	chr12:104530941-104530991	T-47D	breast:	n/a
5	chr12:104531891-104531941	HIPEpiC	eye:	n/a
6	chr12:104532907-104532957	PANC-1	pancreas:	n/a
7	chr12:104532907-104532957	U87	brain:	n/a
8	chr12:104532339-104532389	ProgFib	skin:	n/a
9	chr12:104532011-104532061	HRCEpiC	kidney:	n/a
10	chr12:104531175-104531225	AoSMC	blood vessel:	n/a
11	chr12:104532907-104532957	AG04450	lung:	fetal
12	chr12:104530941-104530991	HepG2	liver:	n/a
13	chr12:104532011-104532061	PrEC	prostate:	n/a
14	chr12:104532011-104532061	BJ	skin:	n/a
15	chr12:104532339-104532389	AG09319	gingival:	n/a
16	chr12:104531891-104531941	T-47D	breast:	n/a
17	chr12:104532339-104532389	NB4	blood:	n/a
18	chr12:104532377-104532427	H1-hESC	embryonic stem cell:	embryo
19	chr12:104532377-104532427	HCPEpiC	choroid plexus:	n/a
20	chr12:104532339-104532389	MCF-7	breast:	n/a
21	chr12:104532907-104532957	HCT-116	colon:	n/a
22	chr12:104531175-104531225	Jurkat	blood:	n/a
23	chr12:104532524-104532574	AG10803	skin:	n/a
24	chr12:104532011-104532061	NB4	blood:	n/a
25	chr12:104531891-104531941	PrEC	prostate:	n/a
26	chr12:104532339-104532389	HCPEpiC	choroid plexus:	n/a
27	chr12:104532524-104532574	T-47D	breast:	n/a
28	chr12:104532377-104532427	NHBE	bronchial:	n/a
29	chr12:104532339-104532389	NHBE	bronchial:	n/a
30	chr12:104531891-104531941	HRPEpiC	eye:	n/a
31	chr12:104531175-104531225	HAEpiC	amniotic membrane:	n/a
32	chr12:104532524-104532574	MCF-7	breast:	n/a
33	chr12:104532377-104532427	HCM	heart:	n/a
34	chr12:104532011-104532061	MCF10A-Er-Src	breast:	n/a
35	chr12:104532907-104532957	MCF-7	breast:	n/a
36	chr12:104532907-104532957	NHBE	bronchial:	n/a
37	chr12:104532907-104532957	ovcar-3	ovarian:	n/a
38	chr12:104530941-104530991	HAEpiC	amniotic membrane:	n/a
39	chr12:104531175-104531225	ovcar-3	ovarian:	n/a
40	chr12:104530941-104530991	BJ	skin:	n/a
41	chr12:104531891-104531941	HRCEpiC	kidney:	n/a
42	chr12:104532011-104532061	IMR90	lung:	fetal
43	chr12:104532524-104532574	LNCaP	prostate:	n/a
44	chr12:104532339-104532389	NH-A	brain:	n/a
45	chr12:104530941-104530991	CMK	blood:	n/a
46	chr12:104532011-104532061	H1-hESC	embryonic stem cell:	embryo
47	chr12:104530941-104530991	HCT-116	colon:	n/a
48	chr12:104530941-104530991	MCF10A-Er-Src	breast:	n/a
49	chr12:104530941-104530991	ProgFib	skin:	n/a
50	chr12:104532339-104532389	HMEC	breast:	n/a

(count:37 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:104531384..104532055-chr2:26568058..26568772,2	Hela-S3	cervix:
2	chr12:104358049..104359986-chr12:104530882..104532737,3	K562	blood:
3	chr12:104529888..104531745-chr12:104641591..104644080,2	MCF-7	breast:
4	chr12:104531440..104533678-chr17:57914653..57916695,2	MCF-7	breast:
5	chr12:104528672..104531458-chr12:104545242..104548166,3	K562	blood:
6	chr12:104348297..104351124-chr12:104530392..104533056,3	MCF-7	breast:
7	chr12:104531360..104532346-chr4:185395679..185396224,2	Hela-S3	cervix:
8	chr12:104530514..104533012-chr12:104679009..104681675,2	K562	blood:
9	chr1:167905681..167906352-chr12:104531146..104532073,2	Hela-S3	cervix:
10	chr12:104234047..104236214-chr12:104531313..104532962,2	MCF-7	breast:
11	chr1:154946283..154947051-chr12:104531811..104532400,2	Hela-S3	cervix:
12	chr12:104487179..104490226-chr12:104527814..104531447,3	K562	blood:
13	chr12:104455182..104458865-chr12:104529769..104532559,3	MCF-7	breast:
14	chr12:104531573..104532274-chr3:49058505..49059412,2	Hela-S3	cervix:
15	chr12:104532395..104534218-chr12:104535636..104537137,2	K562	blood:
16	chr12:104528011..104530810-chr12:104621683..104623795,2	K562	blood:
17	chr12:104530672..104533179-chr6:154830934..154833113,2	MCF-7	breast:
18	chr12:104529689..104531446-chr12:104719514..104721289,2	K562	blood:
19	chr12:104456193..104459744-chr12:104529847..104533076,6	K562	blood:
20	chr12:104530782..104534411-chr12:104679881..104682289,3	K562	blood:
21	chr12:104530438..104533662-chr12:104564030..104567253,5	K562	blood:
22	chr12:104531343..104532062-chr14:24036745..24037302,2	HCT-116	colon:
23	chr12:104529986..104533486-chr12:104678703..104682517,5	MCF-7	breast:
24	chr12:104530239..104532383-chr12:105499797..105502736,2	MCF-7	breast:
25	chr12:104528672..104531458-chr12:104545242..104548166,2	K562	blood:
26	chr12:72079541..72080318-chr12:104531306..104531990,2	NB4	blood:
27	chr12:104481200..104483346-chr12:104529918..104531545,2	K562	blood:
28	chr12:104456335..104459744-chr12:104529847..104533076,5	K562	blood:
29	chr12:104528832..104532197-chr12:105351511..105353407,3	MCF-7	breast:
30	chr12:104510515..104519727-chr12:104525085..104533754,15	MCF-7	breast:
31	chr12:104531449..104532221-chr9:72873633..72874142,2	Hela-S3	cervix:
32	chr12:104490343..104492832-chr12:104530682..104533569,2	MCF-7	breast:
33	chr12:104322684..104325586-chr12:104530441..104532019,2	K562	blood:
34	chr12:104531363..104532174-chr20:25228138..25229130,2	NB4	blood:
35	chr12:104357850..104359549-chr12:104531019..104533949,2	K562	blood:
36	chr12:104356409..104362053-chr12:104528975..104533138,7	MCF-7	breast:
37	chr12:104530429..104534144-chr12:104679811..104684673,6	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GLT8D2-1	chr12:104531919-104532040	NONHSAT030410

No data

Variant related genes	Relation type
NFYB	TF binding region
NFYB	CpG island
ENSG00000198887	chromatin interactions
ENSG00000139291	chromatin interactions
ENSG00000268364	chromatin interactions
ENSG00000166598	chromatin interactions
ENSG00000265072	chromatin interactions
ENSG00000136052	chromatin interactions
ENSG00000257999	chromatin interactions
ENSG00000062716	chromatin interactions
ENSG00000271646	chromatin interactions
ENSG00000178057	chromatin interactions
ENSG00000111727	chromatin interactions
ENSG00000139372	chromatin interactions
ENSG00000257327	chromatin interactions
ENSG00000257193	chromatin interactions
ENSG00000143164	chromatin interactions
ENSG00000198431	chromatin interactions
ENSG00000214198	chromatin interactions
ENSG00000160691	chromatin interactions
ENSG00000204954	chromatin interactions
ENSG00000178149	chromatin interactions
ENSG00000199415	chromatin interactions
ENSG00000173567	chromatin interactions
ENSG00000168310	chromatin interactions
ENSG00000213983	chromatin interactions
ENSG00000153721	chromatin interactions
ENSG00000143158	chromatin interactions
ENSG00000136051	chromatin interactions
ENSG00000100994	chromatin interactions
ENSG00000111696	chromatin interactions
ENSG00000120820	chromatin interactions

Extended variants
information (count: 83 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:83 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs578178561	chr12:104530234-104530235	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
2	rs73392513	chr12:104530258-104530259	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	9 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs563527897	chr12:104530289-104530290	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
4	rs181976999	chr12:104530337-104530338	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
5	rs567571816	chr12:104530367-104530368	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
6	rs542715236	chr12:104530401-104530402	Active TSS Flanking Active TSS Weak transcription Enhancers	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
7	rs559378621	chr12:104530450-104530451	Active TSS Flanking Active TSS Weak transcription Enhancers	Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
8	rs528491874	chr12:104530455-104530456	Active TSS Flanking Active TSS Weak transcription Enhancers	Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
9	rs57998452	chr12:104530467-104530468	Active TSS Flanking Active TSS Weak transcription Enhancers	Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
10	rs551725404	chr12:104530485-104530486	Active TSS Flanking Active TSS Weak transcription Enhancers	Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
11	rs564253212	chr12:104530495-104530496	Active TSS Flanking Active TSS Weak transcription Enhancers	Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
12	rs7979648	chr12:104530548-104530549	Active TSS Flanking Active TSS Weak transcription Enhancers	Chromatin interactive region	13 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs550043090	chr12:104530634-104530635	Active TSS Flanking Active TSS Weak transcription Enhancers	Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
14	rs373828807	chr12:104530721-104530722	Active TSS Flanking Active TSS Weak transcription Enhancers	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
15	rs151293640	chr12:104530737-104530738	Active TSS Flanking Active TSS Weak transcription Enhancers	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
16	rs556078323	chr12:104530742-104530743	Active TSS Flanking Active TSS Weak transcription Enhancers	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
17	rs529054084	chr12:104530753-104530754	Active TSS Flanking Active TSS Weak transcription Enhancers	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
18	rs549111263	chr12:104530792-104530793	Active TSS Flanking Active TSS Weak transcription Enhancers	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
19	rs7979713	chr12:104530806-104530807	Active TSS Weak transcription Flanking Active TSS	Chromatin interactive region	14 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs534348130	chr12:104530809-104530810	Active TSS Weak transcription Flanking Active TSS	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
21	rs557717506	chr12:104530839-104530840	Active TSS Weak transcription Flanking Active TSS	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
22	rs190599220	chr12:104530856-104530857	Active TSS Weak transcription Flanking Active TSS	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
23	rs149505229	chr12:104530881-104530882	Active TSS Weak transcription Flanking Active TSS	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
24	rs201863881	chr12:104530883-104530884	Active TSS Weak transcription Flanking Active TSS	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
25	rs537344273	chr12:104530921-104530922	Active TSS Weak transcription Flanking Active TSS	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
26	rs75168434	chr12:104530942-104530943	Active TSS Weak transcription Flanking Active TSS	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
27	rs573904649	chr12:104530978-104530979	Active TSS Weak transcription Flanking Active TSS	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
28	rs76066636	chr12:104531015-104531016	Active TSS Flanking Active TSS	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
29	rs573266941	chr12:104531020-104531021	Active TSS Flanking Active TSS	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
30	rs545106734	chr12:104531081-104531082	Active TSS Flanking Active TSS	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
31	rs56074043	chr12:104531180-104531181	Active TSS Flanking Active TSS	Chromatin interactive region	16 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs533125222	chr12:104531214-104531215	Active TSS Weak transcription Flanking Active TSS	Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
33	rs113610184	chr12:104531233-104531234	Active TSS Weak transcription Flanking Active TSS	Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
34	rs543746789	chr12:104531282-104531283	Active TSS Weak transcription Flanking Active TSS	Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
35	rs563536349	chr12:104531284-104531285	Active TSS Weak transcription Flanking Active TSS	Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
36	rs529119428	chr12:104531288-104531289	Active TSS Weak transcription Flanking Active TSS	Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
37	rs549174861	chr12:104531314-104531315	Active TSS Weak transcription Flanking Active TSS	Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
38	rs565669947	chr12:104531328-104531329	Active TSS Weak transcription Flanking Active TSS	Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
39	rs528177746	chr12:104531409-104531410	Active TSS Weak transcription Flanking Active TSS	Chromatin interactive region	24 gene(s)	Overlapped CNVs	n/a
40	rs551134855	chr12:104531447-104531448	Active TSS Weak transcription Flanking Active TSS	Chromatin interactive region	25 gene(s)	Overlapped CNVs	n/a
41	rs571224022	chr12:104531490-104531491	Active TSS Weak transcription Flanking Active TSS	Chromatin interactive region	27 gene(s)	Overlapped CNVs	n/a
42	rs536608624	chr12:104531607-104531608	Active TSS Weak transcription Flanking Active TSS	Chromatin interactive region	29 gene(s)	Overlapped CNVs	n/a
43	rs557246408	chr12:104531610-104531611	Active TSS Weak transcription Flanking Active TSS	Chromatin interactive region	29 gene(s)	Overlapped CNVs	n/a
44	rs567590627	chr12:104531686-104531687	Active TSS Weak transcription Flanking Active TSS	Chromatin interactive region	29 gene(s)	Overlapped CNVs	n/a
45	rs375472843	chr12:104531775-104531776	Active TSS Weak transcription Flanking Active TSS	Chromatin interactive region	29 gene(s)	Overlapped CNVs	n/a
46	rs553517345	chr12:104531818-104531819	Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	31 gene(s)	Overlapped CNVs	n/a
47	rs376667886	chr12:104531958-104531959	Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	31 gene(s)	Overlapped CNVs	n/a
48	rs548682471	chr12:104532131-104532132	Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	23 gene(s)	Overlapped CNVs	n/a
49	rs12298853	chr12:104532159-104532160	Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	23 gene(s)	Overlapped CNVs	n/a
50	rs573298273	chr12:104532202-104532203	Active TSS Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	21 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:65)

Disease	PMID	Source
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
T-cell prolymphocytic leukemia	19278963	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
Lung cancer	18438408	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
small cell lung cancer	20016488	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	21390271	CNVD
Cancer	20164919	CNVD
Breast cancer	22032731	CNVD
Cancer	16751803	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Wilms tumour	21544195	CNVD
Ovarian cancer	21720365	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
lymphocytic leukemia	21291569	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	17603634	CNVD
Breast cancer	16397240	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Sudden cardiac death	19188705	CNVD
Breast cancer	17133270	CNVD
Chronic lymphocytic leukemia	21049055	CNVD
Neurocytoma	17123091	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21364760	CNVD
Multiple myeloma	16616336	CNVD
Myelofibrosis	22110671	CNVD

Chromatin state (count:544 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:104493800-104530600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr12:104495600-104530800	Weak transcription	Esophagus	oesophagus
3	chr12:104520000-104530400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr12:104523600-104530600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
5	chr12:104523800-104530400	Enhancers	Fetal Heart	heart
6	chr12:104523800-104530600	Weak transcription	Placenta Amnion	Placenta Amnion
7	chr12:104525200-104530400	Weak transcription	Stomach Mucosa	stomach
8	chr12:104525600-104530400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
9	chr12:104526600-104530400	Weak transcription	Sigmoid Colon	Sigmoid Colon
10	chr12:104526600-104530600	Weak transcription	Psoas Muscle	Psoas
11	chr12:104526600-104531000	Weak transcription	Lung	lung
12	chr12:104526800-104530800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr12:104526800-104530800	Weak transcription	Gastric	stomach
14	chr12:104526800-104531000	Weak transcription	Spleen	Spleen
15	chr12:104527600-104530400	Enhancers	Primary T helper cells PMA-I stimulated	--
16	chr12:104527800-104530400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
17	chr12:104527800-104530600	Weak transcription	Colonic Mucosa	Colon
18	chr12:104528000-104530400	Weak transcription	Duodenum Smooth Muscle	Duodenum
19	chr12:104528000-104530600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
20	chr12:104528000-104530600	Weak transcription	Placenta	Placenta
21	chr12:104528400-104530400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
22	chr12:104528400-104530400	Enhancers	Brain Angular Gyrus	brain
23	chr12:104528600-104530400	Enhancers	Cortex derived primary cultured neurospheres	brain
24	chr12:104528600-104530600	Enhancers	Primary T helper naive cells from peripheral blood	blood
25	chr12:104528600-104530800	Enhancers	Primary T killer memory cells from peripheral blood	blood
26	chr12:104528800-104530400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
27	chr12:104528800-104530400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
28	chr12:104528800-104530400	Enhancers	Adipose Nuclei	Adipose
29	chr12:104528800-104530600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
30	chr12:104528800-104530600	Enhancers	Colon Smooth Muscle	Colon
31	chr12:104529000-104530400	Weak transcription	H9 Cell Line	embryonic stem cell
32	chr12:104529000-104530400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
33	chr12:104529000-104530400	Weak transcription	Left Ventricle	heart
34	chr12:104529000-104530400	Weak transcription	Right Ventricle	heart
35	chr12:104529000-104530400	Weak transcription	Thymus	Thymus
36	chr12:104529000-104530600	Enhancers	Primary T helper cells fromperipheralblood	blood
37	chr12:104529000-104530800	Weak transcription	Ovary	ovary
38	chr12:104529000-104531000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
39	chr12:104529200-104530400	Weak transcription	Primary T cells fromperipheralblood	blood
40	chr12:104529200-104530400	Enhancers	Brain Anterior Caudate	brain
41	chr12:104529200-104530400	Weak transcription	Fetal Muscle Trunk	muscle
42	chr12:104529200-104530400	Weak transcription	Fetal Thymus	thymus
43	chr12:104529200-104530400	Weak transcription	Skeletal Muscle Female	skeletal muscle
44	chr12:104529200-104530400	Enhancers	HepG2	liver
45	chr12:104529200-104530600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr12:104529200-104530800	Weak transcription	Pancreas	Pancrea
47	chr12:104529200-104532400	Active TSS	iPS-20b Cell Line	embryonic stem cell
48	chr12:104529400-104530400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
49	chr12:104529400-104530400	Enhancers	Pancreatic Islets	Pancreatic Islet
50	chr12:104529400-104530400	Enhancers	Monocytes-CD14+_RO01746	blood

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