Variant report

Variant	nsv899541
Chromosome Location	chr12:117414974-117497066
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1430)
CpG islands
(count:3480)
Chromatin interactive
region (count:87)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1430 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:117480848-117481226	K562	blood:	n/a	n/a
2	ARID3A	chr12:117483217-117484132	HepG2	liver:	n/a	n/a
3	ARID3A	chr12:117485974-117486354	HepG2	liver:	n/a	n/a
4	ARID3A	chr12:117480142-117480490	K562	blood:	n/a	n/a
5	ARID3A	chr12:117496405-117496605	HepG2	liver:	n/a	n/a
6	ARID3A	chr12:117463407-117463608	HepG2	liver:	n/a	n/a
7	ATF1	chr12:117443229-117443727	K562	blood:	n/a	n/a
8	ATF1	chr12:117417942-117418220	K562	blood:	n/a	n/a
9	ATF1	chr12:117480768-117481088	K562	blood:	n/a	n/a
10	ATF2	chr12:117463325-117463724	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF3	chr12:117480063-117480501	K562	blood:	n/a	n/a
12	ATF3	chr12:117463242-117463931	A549	lung:	n/a	chr12:117463449-117463458
13	ATF3	chr12:117480160-117480451	K562	blood:	n/a	n/a
14	ATF3	chr12:117443350-117443526	K562	blood:	n/a	n/a
15	ATF3	chr12:117463348-117463642	K562	blood:	n/a	chr12:117463449-117463458
16	ATF3	chr12:117463692-117463900	K562	blood:	n/a	n/a
17	BACH1	chr12:117443378-117443527	K562	blood:	n/a	n/a
18	BACH1	chr12:117490676-117490868	H1-hESC	embryonic stem cell:	n/a	n/a
19	BACH1	chr12:117463352-117463607	H1-hESC	embryonic stem cell:	n/a	n/a
20	BACH1	chr12:117438262-117438324	H1-hESC	embryonic stem cell:	n/a	n/a
21	BACH1	chr12:117480144-117480444	K562	blood:	n/a	chr12:117480343-117480357
22	BACH1	chr12:117458686-117458904	H1-hESC	embryonic stem cell:	n/a	n/a
23	BATF	chr12:117469430-117469618	GM12878	blood:	n/a	n/a
24	BCL11A	chr12:117490524-117490764	GM12878	blood:	n/a	n/a
25	BCL3	chr12:117434525-117434777	GM12878	blood:	n/a	n/a
26	BCL3	chr12:117448059-117448309	GM12878	blood:	n/a	chr12:117448110-117448119
27	BCL3	chr12:117463187-117463766	A549	lung:	n/a	n/a
28	BCL3	chr12:117457701-117457963	GM12878	blood:	n/a	n/a
29	BCL3	chr12:117479931-117480532	K562	blood:	n/a	chr12:117480249-117480256
30	BHLHE40	chr12:117487124-117487373	K562	blood:	n/a	n/a
31	BHLHE40	chr12:117483249-117483514	K562	blood:	n/a	chr12:117483416-117483432
32	BHLHE40	chr12:117482862-117482922	K562	blood:	n/a	n/a
33	BHLHE40	chr12:117443236-117443823	K562	blood:	n/a	n/a
34	BHLHE40	chr12:117488807-117488899	K562	blood:	n/a	n/a
35	BHLHE40	chr12:117463451-117463697	GM12878	blood:	n/a	n/a
36	BHLHE40	chr12:117463293-117463915	K562	blood:	n/a	n/a
37	BHLHE40	chr12:117491467-117491666	K562	blood:	n/a	n/a
38	BHLHE40	chr12:117479834-117481093	K562	blood:	n/a	n/a
39	BRCA1	chr12:117463375-117463719	H1-hESC	embryonic stem cell:	n/a	n/a
40	BRCA1	chr12:117482821-117482889	HepG2	liver:	n/a	n/a
41	BRCA1	chr12:117484045-117484078	HepG2	liver:	n/a	n/a
42	BRCA1	chr12:117458672-117458675	H1-hESC	embryonic stem cell:	n/a	n/a
43	CBX3	chr12:117463286-117463670	K562	blood:	n/a	n/a
44	CBX3	chr12:117480090-117480450	K562	blood:	n/a	n/a
45	CBX3	chr12:117479967-117480589	K562	blood:	n/a	n/a
46	CBX3	chr12:117484681-117484988	K562	blood:	n/a	n/a
47	CCNT2	chr12:117443291-117443578	K562	blood:	n/a	chr12:117443386-117443406
48	CCNT2	chr12:117479701-117481115	K562	blood:	n/a	chr12:117480239-117480259 chr12:117480086-117480095 chr12:117480092-117480101
49	CCNT2	chr12:117486450-117486728	K562	blood:	n/a	n/a
50	CEBPB	chr12:117444626-117444876	HepG2	liver:	n/a	chr12:117444765-117444776

(count:3480 , 50 per page) page: 1 2 3 4 5 6 7 ... 70

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:117470875-117470925	HRPEpiC	eye:	n/a
2	chr12:117477105-117477155	HMEC	breast:	n/a
3	chr12:117484926-117484976	NHDF-neo	bronchial:	n/a
4	chr12:117470875-117470925	HRPEpiC	eye:	n/a
5	chr12:117477105-117477155	HMEC	breast:	n/a
6	chr12:117484926-117484976	NHDF-neo	bronchial:	n/a
7	chr12:117457846-117457896	T-47D	breast:	n/a
8	chr12:117468345-117468395	HRPEpiC	eye:	n/a
9	chr12:117483310-117483360	HUVEC	blood vessel:	n/a
10	chr12:117477000-117477050	U87	brain:	n/a
11	chr12:117415439-117415489	T-47D	breast:	n/a
12	chr12:117470549-117470599	Jurkat	blood:	n/a
13	chr12:117473375-117473425	NHBE	bronchial:	n/a
14	chr12:117470875-117470925	AG09319	gingival:	n/a
15	chr12:117425016-117425066	HMEC	breast:	n/a
16	chr12:117470568-117470618	GM12878	blood:	n/a
17	chr12:117474507-117474557	GM12878	blood:	n/a
18	chr12:117480333-117480383	SK-N-SH	brain:	n/a
19	chr12:117468345-117468395	AG04449	skin:	fetal
20	chr12:117476838-117476888	HNPCEpiC	eye:	n/a
21	chr12:117477837-117477887	SKMC	muscle:	n/a
22	chr12:117470875-117470925	HepG2	liver:	n/a
23	chr12:117470922-117470972	A549	lung:	n/a
24	chr12:117425053-117425103	GM06990	blood:	n/a
25	chr12:117483310-117483360	ovcar-3	ovarian:	n/a
26	chr12:117470922-117470972	CMK	blood:	n/a
27	chr12:117473375-117473425	MCF10A-Er-Src	breast:	n/a
28	chr12:117415439-117415489	AoSMC	blood vessel:	n/a
29	chr12:117429362-117429412	NH-A	brain:	n/a
30	chr12:117484975-117485025	AG04449	skin:	fetal
31	chr12:117470922-117470972	SK-N-MC	brain:	n/a
32	chr12:117470568-117470618	GM19239	blood:	n/a
33	chr12:117448155-117448205	HCF	heart:	n/a
34	chr12:117470541-117470591	CMK	blood:	n/a
35	chr12:117482953-117483003	HRPEpiC	eye:	n/a
36	chr12:117477926-117477976	LNCaP	prostate:	n/a
37	chr12:117484926-117484976	HCT-116	colon:	n/a
38	chr12:117476704-117476754	GM12891	blood:	n/a
39	chr12:117470541-117470591	AG10803	skin:	n/a
40	chr12:117470541-117470591	LNCaP	prostate:	n/a
41	chr12:117470549-117470599	HEEpiC	esophagus:	n/a
42	chr12:117448211-117448261	A549	lung:	n/a
43	chr12:117468061-117468111	GM19239	blood:	n/a
44	chr12:117465598-117465648	CMK	blood:	n/a
45	chr12:117471115-117471165	NHDF-neo	bronchial:	n/a
46	chr12:117468289-117468339	HCPEpiC	choroid plexus:	n/a
47	chr12:117471115-117471165	ovcar-3	ovarian:	n/a
48	chr12:117476704-117476754	AG10803	skin:	n/a
49	chr12:117457899-117457949	HNPCEpiC	eye:	n/a
50	chr12:117457846-117457896	U87	brain:	n/a

(count:87 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr10:108351027..108351716-chr12:117439841..117440341,2	Hela-S3	cervix:
2	chr12:117470652..117475607-chr12:117477009..117480553,6	K562	blood:
3	chr12:117478764..117480337-chr12:117507542..117509492,2	K562	blood:
4	chr12:117463007..117463900-chr12:117588701..117589613,6	MCF-7	breast:
5	chr12:117427238..117428899-chr12:117435662..117438288,2	MCF-7	breast:
6	chr12:117491735..117493478-chr12:117493930..117496851,2	MCF-7	breast:
7	chr12:117468241..117470806-chr12:117471546..117474082,2	K562	blood:
8	chr12:117438206..117440859-chr12:117443702..117446007,2	K562	blood:
9	chr12:117421081..117423029-chr12:117430032..117431704,2	K562	blood:
10	chr12:117478356..117481644-chr12:117536617..117538572,3	K562	blood:
11	chr12:117463032..117464059-chr12:117588578..117590000,12	K562	blood:
12	chr12:117447389..117449402-chr12:117456865..117458856,2	MCF-7	breast:
13	chr12:117468241..117470806-chr12:117471546..117474082,2	K562	blood:
14	chr12:117488907..117491503-chr12:117528799..117530966,2	K562	blood:
15	chr12:117421809..117423733-chr12:117438090..117440215,2	MCF-7	breast:
16	chr12:117461340..117464538-chr12:117578917..117582364,3	MCF-7	breast:
17	chr12:117477087..117480724-chr12:117486826..117489814,3	MCF-7	breast:
18	chr12:117416955..117418879-chr12:117430472..117432333,2	K562	blood:
19	chr12:117454524..117457416-chr12:117594664..117596732,2	K562	blood:
20	chr12:117495577..117497098-chr12:117535967..117538055,2	K562	blood:
21	chr12:117424615..117427495-chr12:117434395..117436696,2	MCF-7	breast:
22	chr12:117461681..117464080-chr12:117470751..117473024,2	MCF-7	breast:
23	chr12:117447389..117449402-chr12:117456865..117458856,2	MCF-7	breast:
24	chr12:117455374..117458365-chr12:117461422..117463402,2	MCF-7	breast:
25	chr12:117463072..117464125-chr12:117557237..117558458,16	MCF-7	breast:
26	chr12:117463061..117463973-chr12:117592706..117593552,4	K562	blood:
27	chr12:117442427..117445023-chr12:117448481..117451118,2	K562	blood:
28	chr12:117462662..117464720-chr12:117586991..117588878,2	MCF-7	breast:
29	chr12:117463029..117464320-chr12:117592692..117593657,7	MCF-7	breast:
30	chr12:117413641..117415304-chr12:117416885..117418716,2	K562	blood:
31	chr12:117470409..117472666-chr12:117473842..117475716,2	MCF-7	breast:
32	chr12:117461681..117464080-chr12:117470751..117473024,2	MCF-7	breast:
33	chr12:117473852..117475862-chr12:117477409..117479027,2	K562	blood:
34	chr12:117469991..117472353-chr12:117476644..117478230,2	MCF-7	breast:
35	chr12:117439692..117442558-chr12:117449975..117451489,2	K562	blood:
36	chr12:117474107..117476260-chr12:117479053..117480965,2	K562	blood:
37	chr12:117371490..117373713-chr12:117436920..117439603,2	K562	blood:
38	chr12:117437746..117440229-chr12:117441303..117443639,2	K562	blood:
39	chr12:117441591..117444664-chr12:117447106..117450120,5	MCF-7	breast:
40	chr12:117421081..117423029-chr12:117430032..117431704,2	K562	blood:
41	chr12:117462019..117462826-chr12:117557173..117558198,3	MCF-7	breast:
42	chr12:117465400..117467600-chr12:117591439..117594342,2	MCF-7	breast:
43	chr12:117438206..117440859-chr12:117443702..117446007,2	K562	blood:
44	chr12:117439692..117442558-chr12:117449975..117451489,2	K562	blood:
45	chr12:117406724..117409328-chr12:117437750..117440226,2	MCF-7	breast:
46	chr12:117469818..117471937-chr12:117535660..117537284,2	MCF-7	breast:
47	chr12:117477087..117480724-chr12:117486826..117489814,3	MCF-7	breast:
48	chr12:117478574..117480262-chr12:117481796..117483489,2	K562	blood:
49	chr12:117447732..117449605-chr12:117449689..117452738,3	K562	blood:
50	chr12:117416955..117418879-chr12:117430472..117432333,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TESC-3	chr12:117468955-117470651	NONHSAT030978
2	lnc-TESC-4	chr12:117468114-117468161	NONHSAT030977
3	lnc-TESC-4	chr12:117468512-117468878	NONHSAT030977

No data

Variant related genes	Relation type
FBXW8	TF binding region
TESC	TF binding region
ENSG00000257279	TF binding region
FBXW8	CpG island
TESC	CpG island
ENSG00000257279	CpG island
ENSG00000143742	chromatin interactions
ENSG00000257279	chromatin interactions
ENSG00000135108	chromatin interactions
ENSG00000174989	chromatin interactions
ENSG00000258285	chromatin interactions
ENSG00000088992	chromatin interactions

Extended variants
information (count: 3516 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:3516 , 50 per page) page: 1 2 3 4 5 6 7 ... 71

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4766819	chr12:117414974-117414975	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs569322556	chr12:117414981-117414982	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs549972651	chr12:117415058-117415059	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs200011709	chr12:117415075-117415076	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs76312021	chr12:117415084-117415085	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs76411180	chr12:117415085-117415086	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs139919293	chr12:117415110-117415111	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs558519571	chr12:117415141-117415142	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs60192526	chr12:117415142-117415143	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs118026254	chr12:117415150-117415151	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs145344777	chr12:117415162-117415163	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs573722302	chr12:117415225-117415226	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs539537528	chr12:117415256-117415257	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs115228650	chr12:117415293-117415294	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs555941305	chr12:117415323-117415324	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs61254876	chr12:117415343-117415344	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs564745317	chr12:117415397-117415398	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs35393928	chr12:117415439-117415440	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	CpG island	1 gene(s)	Overlapped CNVs	n/a
19	rs564868920	chr12:117415440-117415441	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	CpG island	1 gene(s)	Overlapped CNVs	n/a
20	rs181236930	chr12:117415526-117415527	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs541729637	chr12:117415536-117415537	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs74882149	chr12:117415568-117415569	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs530204364	chr12:117415587-117415588	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs550351476	chr12:117415757-117415758	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs149790289	chr12:117415782-117415783	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs145572236	chr12:117415802-117415803	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs550257820	chr12:117415865-117415866	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs552282100	chr12:117415869-117415870	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs186580499	chr12:117415885-117415886	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs534715496	chr12:117415945-117415946	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs76663476	chr12:117415993-117415994	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs140331984	chr12:117416009-117416010	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs372212615	chr12:117416017-117416018	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs144165405	chr12:117416051-117416052	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs560689548	chr12:117416076-117416077	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs556312819	chr12:117416124-117416125	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs78538428	chr12:117416154-117416155	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs546602592	chr12:117416158-117416159	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs79934608	chr12:117416311-117416312	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs190587782	chr12:117416341-117416342	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs572036731	chr12:117416346-117416347	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs140845850	chr12:117416349-117416350	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs143034072	chr12:117416388-117416389	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs561374456	chr12:117416446-117416447	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs371844474	chr12:117416458-117416459	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs567025160	chr12:117416487-117416488	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs367798347	chr12:117416493-117416494	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs530413296	chr12:117416514-117416515	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs115011155	chr12:117416558-117416559	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs371883999	chr12:117416594-117416595	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:70)

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
small cell lung cancer	20016488	CNVD
Glioblastoma multiforme	21390271	CNVD
Cancer	20164919	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
lymphocytic leukemia	21291569	CNVD
Breast cancer	17603634	CNVD
Breast cancer	16397240	CNVD
Sudden cardiac death	19188705	CNVD
Breast cancer	17133270	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Schizophrenia	18923514	CNVD
Schizophrenia	22241247	CNVD
Cryptorchidism	21048976	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Neuroblastoma	18923191	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Neuroblastoma	20406844	CNVD
Medulloblastoma	16783165	CNVD
mental retardation	16760730	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21364760	CNVD
Lung adenocarcinoma	21045234	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21806811	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:2883 , 50 per page) page: 1 2 3 4 5 6 7 ... 58

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:117384600-117427400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
2	chr12:117384800-117450400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
3	chr12:117387800-117463600	Weak transcription	HMEC	breast
4	chr12:117393800-117471000	Weak transcription	Small Intestine	intestine
5	chr12:117394600-117415400	Weak transcription	HSMMtube	muscle
6	chr12:117397000-117429200	Weak transcription	Right Ventricle	heart
7	chr12:117397000-117442400	Weak transcription	Colonic Mucosa	Colon
8	chr12:117398200-117417400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
9	chr12:117400400-117417800	Weak transcription	K562	blood
10	chr12:117400800-117415400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
11	chr12:117402200-117417200	Weak transcription	Stomach Mucosa	stomach
12	chr12:117403400-117416800	Weak transcription	HUVEC	blood vessel
13	chr12:117403400-117418000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
14	chr12:117403400-117423200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
15	chr12:117403600-117420400	Weak transcription	Rectal Smooth Muscle	rectum
16	chr12:117404600-117427000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
17	chr12:117404600-117442400	Weak transcription	HepG2	liver
18	chr12:117404800-117426400	Weak transcription	Rectal Mucosa Donor 31	rectum
19	chr12:117405400-117418000	Weak transcription	Placenta Amnion	Placenta Amnion
20	chr12:117405600-117420400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
21	chr12:117405600-117442400	Weak transcription	Primary T helper cells PMA-I stimulated	--
22	chr12:117408000-117420200	Weak transcription	Colon Smooth Muscle	Colon
23	chr12:117408000-117427600	Weak transcription	Dnd41	blood
24	chr12:117408200-117417400	Weak transcription	Gastric	stomach
25	chr12:117408200-117424800	Weak transcription	Brain Hippocampus Middle	brain
26	chr12:117408200-117426400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
27	chr12:117408200-117427000	Weak transcription	Skeletal Muscle Female	skeletal muscle
28	chr12:117408200-117429600	Weak transcription	Brain Substantia Nigra	brain
29	chr12:117408200-117442400	Weak transcription	Skeletal Muscle Male	skeletal muscle
30	chr12:117408400-117420200	Weak transcription	Fetal Brain Male	brain
31	chr12:117408400-117420400	Weak transcription	Fetal Lung	lung
32	chr12:117408400-117432600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
33	chr12:117408400-117452200	Weak transcription	Thymus	Thymus
34	chr12:117408600-117415400	Weak transcription	HUES6 Cell Line	embryonic stem cell
35	chr12:117408600-117416400	Weak transcription	Brain Germinal Matrix	brain
36	chr12:117408600-117420800	Weak transcription	Fetal Heart	heart
37	chr12:117408600-117422400	Weak transcription	Fetal Intestine Small	intestine
38	chr12:117408800-117415400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
39	chr12:117409000-117427200	Weak transcription	H9 Cell Line	embryonic stem cell
40	chr12:117409800-117415200	Weak transcription	GM12878-XiMat	blood
41	chr12:117410800-117416200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
42	chr12:117411000-117424400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr12:117411200-117423200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
44	chr12:117411200-117423200	Weak transcription	Adipose Nuclei	Adipose
45	chr12:117411600-117415200	Weak transcription	HUES64 Cell Line	embryonic stem cell
46	chr12:117411600-117415400	Weak transcription	HUES48 Cell Line	embryonic stem cell
47	chr12:117411600-117415400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
48	chr12:117411600-117417000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
49	chr12:117411600-117420800	Weak transcription	H1 Cell Line	embryonic stem cell
50	chr12:117411600-117423000	Weak transcription	Cortex derived primary cultured neurospheres	brain

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