Variant report

Variant	esv3377733
Chromosome Location	chr12:57399235-57401433
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:520)
CpG islands
(count:428)
Chromatin interactive
region (count:33)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:520 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr12:57399638-57399657	K562	blood:	n/a	n/a
2	BHLHE40	chr12:57399193-57399331	K562	blood:	n/a	n/a
3	BHLHE40	chr12:57400300-57400537	GM12878	blood:	n/a	n/a
4	BRCA1	chr12:57399804-57399875	Hela-S3	cervix:	n/a	n/a
5	CCNT2	chr12:57399659-57400599	K562	blood:	n/a	n/a
6	CEBPB	chr12:57400165-57400276	Hela-S3	cervix:	n/a	n/a
7	CEBPD	chr12:57400092-57400392	HepG2	liver:	n/a	n/a
8	CHD1	chr12:57400533-57400610	GM12878	blood:	n/a	n/a
9	CREB1	chr12:57400115-57400597	A549	lung:	n/a	n/a
10	CTCF	chr12:57399700-57399850	HFF	foreskin:	n/a	chr12:57399761-57399770 chr12:57399757-57399770
11	CTCF	chr12:57400340-57400490	AoAF	blood vessel:	n/a	n/a
12	CTCF	chr12:57399860-57400010	SK-N-SH_RA	brain:	n/a	chr12:57399931-57399949
13	CTCF	chr12:57400380-57400530	BJ	skin:	n/a	n/a
14	CTCF	chr12:57399920-57400070	WERI-Rb-1	eye:	n/a	chr12:57399931-57399949
15	CTCF	chr12:57400360-57400510	AG04449	skin:	n/a	n/a
16	CTCF	chr12:57399860-57400010	GM12878	blood:	n/a	chr12:57399931-57399949
17	CTCF	chr12:57400440-57400590	HUVEC	blood vessel:	n/a	n/a
18	CTCF	chr12:57399580-57399730	GM06990	blood:	n/a	n/a
19	CTCF	chr12:57400360-57400510	AG10803	skin:	n/a	n/a
20	CTCF	chr12:57400270-57400567	NHEK	skin:	n/a	n/a
21	CTCF	chr12:57400226-57400584	Lung_OC	lung:	n/a	n/a
22	CTCF	chr12:57400380-57400530	HCT-116	colon:	n/a	n/a
23	CTCF	chr12:57400920-57401070	AG09319	gingival:	n/a	n/a
24	CTCF	chr12:57399770-57400738	GM12878	blood:	n/a	chr12:57399931-57399949
25	CTCF	chr12:57400253-57400556	LNCaP	prostate:	n/a	n/a
26	CTCF	chr12:57401048-57401085	GM19240	blood:	n/a	n/a
27	CTCF	chr12:57400276-57400620	ECC-1	luminal epithelium:	n/a	n/a
28	CTCF	chr12:57400380-57400530	AG09309	skin:	n/a	n/a
29	CTCF	chr12:57399760-57399910	GM12873	blood:	n/a	chr12:57399761-57399770
30	CTCF	chr12:57399112-57401337	SK-N-SH	brain:	n/a	chr12:57399761-57399770 chr12:57399931-57399949 chr12:57399757-57399770
31	CTCF	chr12:57399920-57400070	HFF	foreskin:	n/a	chr12:57399931-57399949
32	CTCF	chr12:57400220-57400556	MCF-7	breast:	n/a	n/a
33	CTCF	chr12:57401315-57401358	HUVEC	blood vessel:	n/a	n/a
34	CTCF	chr12:57401060-57401210	GM12878	blood:	n/a	n/a
35	CTCF	chr12:57400420-57400570	HMF	breast:	n/a	n/a
36	CTCF	chr12:57400380-57400530	GM12869	blood:	n/a	n/a
37	CTCF	chr12:57400245-57400582	Gliobla	brain:	n/a	n/a
38	CTCF	chr12:57400259-57400561	MCF-7	breast:	n/a	n/a
39	CTCF	chr12:57400380-57400530	HCM	heart:	n/a	n/a
40	CTCF	chr12:57399920-57400070	GM12867	blood:	n/a	chr12:57399931-57399949
41	CTCF	chr12:57399940-57400090	Caco-2	colon:	n/a	n/a
42	CTCF	chr12:57400400-57400550	Caco-2	colon:	n/a	n/a
43	CTCF	chr12:57399892-57399965	NHEK	skin:	n/a	chr12:57399931-57399949
44	CTCF	chr12:57400000-57400150	HMEC	breast:	n/a	n/a
45	CTCF	chr12:57400266-57400573	A549	lung:	n/a	n/a
46	CTCF	chr12:57401380-57401530	AG09309	skin:	n/a	n/a
47	CTCF	chr12:57400400-57400550	HepG2	liver:	n/a	n/a
48	CTCF	chr12:57399860-57400010	Hela-S3	cervix:	n/a	chr12:57399931-57399949
49	CTCF	chr12:57399882-57399998	Fibrobl	skin:	n/a	chr12:57399931-57399949
50	CTCF	chr12:57400380-57400530	HFF-Myc	foreskin:	n/a	n/a

(count:428 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:57399475-57399525	GM12892	blood:	n/a
2	chr12:57399475-57399525	GM12892	blood:	n/a
3	chr12:57400201-57400251	HL-60	blood:	n/a
4	chr12:57399475-57399525	HCT-116	colon:	n/a
5	chr12:57400201-57400251	MCF-7	breast:	n/a
6	chr12:57399932-57399982	U87	brain:	n/a
7	chr12:57400517-57400567	PANC-1	pancreas:	n/a
8	chr12:57400910-57400960	Caco-2	colon:	n/a
9	chr12:57400532-57400582	NB4	blood:	n/a
10	chr12:57399475-57399525	GM06990	blood:	n/a
11	chr12:57399475-57399525	ECC-1	luminal epithelium:	n/a
12	chr12:57399475-57399525	HRPEpiC	eye:	n/a
13	chr12:57399932-57399982	NT2-D1	testis:	n/a
14	chr12:57399475-57399525	HL-60	blood:	n/a
15	chr12:57400033-57400083	MCF-7	breast:	n/a
16	chr12:57400033-57400083	BJ	skin:	n/a
17	chr12:57400517-57400567	H1-hESC	embryonic stem cell:	embryo
18	chr12:57400517-57400567	HEK293	kidney:	embryo
19	chr12:57399475-57399525	T-47D	breast:	n/a
20	chr12:57400033-57400083	HRPEpiC	eye:	n/a
21	chr12:57400532-57400582	HMEC	breast:	n/a
22	chr12:57399475-57399525	HNPCEpiC	eye:	n/a
23	chr12:57399932-57399982	HRPEpiC	eye:	n/a
24	chr12:57400517-57400567	Caco-2	colon:	n/a
25	chr12:57400033-57400083	MCF10A-Er-Src	breast:	n/a
26	chr12:57400532-57400582	PANC-1	pancreas:	n/a
27	chr12:57400201-57400251	HCF	heart:	n/a
28	chr12:57400201-57400251	AG04450	lung:	fetal
29	chr12:57400033-57400083	CMK	blood:	n/a
30	chr12:57400201-57400251	MCF10A-Er-Src	breast:	n/a
31	chr12:57400517-57400567	PrEC	prostate:	n/a
32	chr12:57399932-57399982	CMK	blood:	n/a
33	chr12:57400532-57400582	HNPCEpiC	eye:	n/a
34	chr12:57399932-57399982	HRE	kidney:	n/a
35	chr12:57400910-57400960	IMR90	lung:	fetal
36	chr12:57400033-57400083	ECC-1	luminal epithelium:	n/a
37	chr12:57399932-57399982	A549	lung:	n/a
38	chr12:57400532-57400582	NHBE	bronchial:	n/a
39	chr12:57400201-57400251	NHBE	bronchial:	n/a
40	chr12:57400517-57400567	GM12878	blood:	n/a
41	chr12:57400517-57400567	AG10803	skin:	n/a
42	chr12:57400033-57400083	HPAEpiC	pulmonary alveolar:	n/a
43	chr12:57399932-57399982	Caco-2	colon:	n/a
44	chr12:57400517-57400567	AoSMC	blood vessel:	n/a
45	chr12:57400532-57400582	MCF-7	breast:	n/a
46	chr12:57399932-57399982	Hela-S3	cervix:	n/a
47	chr12:57399932-57399982	LNCaP	prostate:	n/a
48	chr12:57399475-57399525	HCF	heart:	n/a
49	chr12:57399932-57399982	HUVEC	blood vessel:	n/a
50	chr12:57400033-57400083	HMEC	breast:	n/a

(count:33 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:57388586..57390855-chr12:57398700..57400334,2	MCF-7	breast:
2	chr12:57398801..57400719-chr12:57521892..57524489,2	K562	blood:
3	chr12:57079674..57082070-chr12:57399337..57401813,2	MCF-7	breast:
4	chr12:57393282..57404587-chr12:57480276..57487045,17	MCF-7	breast:
5	chr12:57401062..57403586-chr12:57443531..57445690,2	K562	blood:
6	chr12:57398801..57400743-chr12:57521280..57524489,3	K562	blood:
7	chr12:57328529..57331302-chr12:57397442..57399597,2	K562	blood:
8	chr12:57208652..57211649-chr12:57400482..57401997,2	MCF-7	breast:
9	chr12:56709311..56709830-chr12:57399980..57400910,2	MCF-7	breast:
10	chr12:57400251..57400827-chr12:57454532..57455160,2	MCF-7	breast:
11	chr12:57400180..57401732-chr12:57514933..57516523,2	K562	blood:
12	chr12:57400427..57402065-chr12:57502881..57505557,2	MCF-7	breast:
13	chr12:57145657..57146209-chr12:57399868..57400428,2	MCF-7	breast:
14	chr12:57398945..57400725-chr12:57479656..57482846,3	MCF-7	breast:
15	chr12:57401104..57405112-chr12:57417084..57419989,4	MCF-7	breast:
16	chr12:57400299..57402687-chr12:57590687..57592398,2	MCF-7	breast:
17	chr12:57401074..57403067-chr12:57449205..57451549,2	MCF-7	breast:
18	chr12:57399976..57400833-chr12:57424825..57425490,2	MCF-7	breast:
19	chr12:57398623..57401161-chr12:57471695..57473634,2	MCF-7	breast:
20	chr12:57401359..57402312-chr12:57576362..57577409,4	K562	blood:
21	chr12:57143921..57145852-chr12:57400394..57401927,2	MCF-7	breast:
22	chr12:57387865..57389441-chr12:57397385..57400000,2	MCF-7	breast:
23	chr12:57400260..57400857-chr17:59486758..59487383,2	MCF-7	breast:
24	chr12:57399687..57402362-chr12:57503183..57504772,2	K562	blood:
25	chr12:57400549..57402896-chr12:57450333..57452770,2	K562	blood:
26	chr12:57156105..57159269-chr12:57397404..57399756,3	MCF-7	breast:
27	chr12:57400522..57402479-chr12:57481021..57483071,2	K562	blood:
28	chr12:57391872..57393756-chr12:57396852..57399848,3	MCF-7	breast:
29	chr12:57156641..57157497-chr12:57399996..57400652,4	MCF-7	breast:
30	chr12:57387906..57390511-chr12:57397113..57399699,3	K562	blood:
31	chr12:57029519..57031379-chr12:57397425..57399407,2	K562	blood:
32	chr12:57400458..57402915-chr12:57407849..57410746,2	MCF-7	breast:
33	chr12:57400361..57402022-chr12:57481021..57483106,2	K562	blood:

No data

Variant related genes	Relation type
ZBTB39	TF binding region
ZBTB39	CpG island
ENSG00000166866	chromatin interactions
ENSG00000258442	chromatin interactions
ENSG00000110958	chromatin interactions
ENSG00000198056	chromatin interactions
ENSG00000166881	chromatin interactions
ENSG00000076108	chromatin interactions
ENSG00000166888	chromatin interactions
ENSG00000166863	chromatin interactions
ENSG00000025423	chromatin interactions
ENSG00000257727	chromatin interactions
ENSG00000166886	chromatin interactions
ENSG00000166856	chromatin interactions
ENSG00000144785	chromatin interactions
ENSG00000268162	chromatin interactions
ENSG00000123384	chromatin interactions
ENSG00000263832	chromatin interactions

Extended variants
information (count: 57 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:57 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs74600314	chr12:57399266-57399267	Flanking Active TSS Weak transcription Active TSS Enhancers Genic enhancers	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
2	rs551205960	chr12:57399296-57399297	Flanking Active TSS Weak transcription Active TSS Enhancers Genic enhancers	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
3	rs555888142	chr12:57399326-57399327	Flanking Active TSS Weak transcription Active TSS Enhancers Genic enhancers	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
4	rs571522983	chr12:57399333-57399334	Flanking Active TSS Weak transcription Active TSS Enhancers Genic enhancers	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
5	rs556051627	chr12:57399364-57399365	Flanking Active TSS Weak transcription Active TSS Enhancers Genic enhancers	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
6	rs538923485	chr12:57399409-57399410	Active TSS Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
7	rs144803141	chr12:57399442-57399443	Active TSS Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
8	rs192503159	chr12:57399450-57399451	Active TSS Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
9	rs61939636	chr12:57399466-57399467	Active TSS Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	9 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs555804581	chr12:57399495-57399496	Active TSS Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
11	rs574053934	chr12:57399532-57399533	Active TSS Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
12	rs7972615	chr12:57399556-57399557	Active TSS Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	9 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs538573158	chr12:57399620-57399621	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
14	rs379760	chr12:57399808-57399809	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Enhancers	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
15	rs370742124	chr12:57399833-57399834	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Enhancers	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
16	rs553418737	chr12:57399891-57399892	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Enhancers	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
17	rs573466897	chr12:57399926-57399927	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Enhancers	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
18	rs562533885	chr12:57399993-57399994	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Enhancers	Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
19	rs185869776	chr12:57400033-57400034	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Weak transcription Enhancers	Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
20	rs545275118	chr12:57400080-57400081	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Weak transcription Enhancers	Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
21	rs560445583	chr12:57400209-57400210	Weak transcription Active TSS Transcr. at gene 5' and 3' Enhancers Flanking Active TSS	Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
22	rs527850421	chr12:57400283-57400284	Weak transcription Active TSS Transcr. at gene 5' and 3' Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
23	rs374587633	chr12:57400419-57400420	Weak transcription Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
24	rs549331135	chr12:57400443-57400444	Weak transcription Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
25	rs145398215	chr12:57400517-57400518	Weak transcription Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
26	rs534330916	chr12:57400526-57400527	Weak transcription Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
27	rs377373661	chr12:57400528-57400529	Weak transcription Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
28	rs572055012	chr12:57400662-57400663	Weak transcription Active TSS Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
29	rs28665019	chr12:57400689-57400690	Weak transcription Active TSS Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
30	rs549430134	chr12:57400735-57400736	Weak transcription Active TSS Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
31	rs571243809	chr12:57400801-57400802	Weak transcription Enhancers Active TSS Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
32	rs538675088	chr12:57400829-57400830	Weak transcription Enhancers Active TSS Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
33	rs554076550	chr12:57400833-57400834	Weak transcription Enhancers Active TSS Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
34	rs151065431	chr12:57400867-57400868	Weak transcription Enhancers Active TSS Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
35	rs11616016	chr12:57400884-57400885	Weak transcription Enhancers Active TSS Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
36	rs536400727	chr12:57400888-57400889	Weak transcription Enhancers Active TSS Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
37	rs554478027	chr12:57400928-57400929	Weak transcription Enhancers Active TSS Genic enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
38	rs56178718	chr12:57400954-57400955	Weak transcription Enhancers Active TSS Genic enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
39	rs574197081	chr12:57400982-57400983	Weak transcription Enhancers Active TSS Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
40	rs576228457	chr12:57401014-57401015	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
41	rs189128992	chr12:57401046-57401047	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
42	rs557573355	chr12:57401053-57401054	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
43	rs569434117	chr12:57401054-57401055	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
44	rs116009383	chr12:57401082-57401083	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
45	rs117943989	chr12:57401098-57401099	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
46	rs577599609	chr12:57401099-57401100	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
47	rs3759138	chr12:57401111-57401112	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
48	rs368977784	chr12:57401194-57401195	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
49	rs140930393	chr12:57401195-57401196	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
50	rs149784339	chr12:57401212-57401213	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:91)

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
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
Lissencephaly	21572526	CNVD
Lung cancer	18438408	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Breast cancer	19602461	CNVD
Breast cancer	17899364	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	21364760	CNVD
Prostate cancer	18632612	CNVD
Metanephric adenoma	20802469	CNVD
Glioblastoma multiforme	17387387	CNVD
liposarcomas	17372913	CNVD
Non-small cell lung cancer	24170126	CNVD
Cancer	16751803	CNVD
Bladder cancer	21909424	CNVD
Intracranial aneurysm	16715129	CNVD
Breast cancer	17661082	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	21785460	CNVD
small cell lung cancer	20016488	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Hodgkin''s lymphoma	18179710	CNVD
Autism	20531469	CNVD
Rhabdomyosarcoma	16790082	CNVD
Renal cell carcinoma	18765545	CNVD
Urothelial cell carcinoma	18451213	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	21138945	CNVD
Glioblastoma multiforme	21390271	CNVD
Cancer	20164919	CNVD
Leukemia	18628472	CNVD
Glioblastoma multiforme	22291905	CNVD
Glioblastoma multiforme	19435819	CNVD
Myelofibrosis	22110671	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
Follicular lymphoma	18703704	CNVD
Acute myeloid leukemia	21251322	CNVD
Glycogen storage disease	18421352	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Glioblastoma multiforme	20080666	CNVD
Medulloblastoma	19270706	CNVD
Breast cancer	17133270	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Osteosarcoma	21215367	CNVD

Chromatin state (count:495 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:57395800-57399400	Weak transcription	Right Atrium	heart
2	chr12:57396800-57399600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
3	chr12:57398400-57399400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr12:57398400-57399400	Enhancers	Primary T helper naive cells from peripheral blood	blood
5	chr12:57398400-57399400	Genic enhancers	Primary T helper 17 cells PMA-I stimulated	--
6	chr12:57398600-57399400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr12:57398600-57399400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr12:57398600-57399400	Enhancers	Primary T cells fromperipheralblood	blood
9	chr12:57398600-57399400	Enhancers	Primary T helper cells fromperipheralblood	blood
10	chr12:57398600-57399400	Enhancers	Brain Inferior Temporal Lobe	brain
11	chr12:57398600-57399400	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
12	chr12:57398600-57399400	Weak transcription	Pancreas	Pancrea
13	chr12:57398600-57399600	Enhancers	Primary B cells from peripheral blood	blood
14	chr12:57398600-57399600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
15	chr12:57398600-57399600	Weak transcription	Aorta	Aorta
16	chr12:57398600-57399600	Weak transcription	Gastric	stomach
17	chr12:57398600-57399600	Enhancers	Spleen	Spleen
18	chr12:57398600-57399800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
19	chr12:57398600-57400800	Active TSS	H1 Cell Line	embryonic stem cell
20	chr12:57398800-57399400	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
21	chr12:57398800-57399400	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr12:57398800-57399400	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
23	chr12:57398800-57399400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
24	chr12:57398800-57399400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
25	chr12:57398800-57399400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
26	chr12:57398800-57399400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
27	chr12:57398800-57399400	Enhancers	Primary T regulatory cells fromperipheralblood	blood
28	chr12:57398800-57399400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
29	chr12:57398800-57399400	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
30	chr12:57398800-57399400	Enhancers	Brain Substantia Nigra	brain
31	chr12:57398800-57399400	Weak transcription	Fetal Muscle Trunk	muscle
32	chr12:57398800-57399400	Enhancers	Placenta	Placenta
33	chr12:57398800-57399400	Enhancers	Fetal Thymus	thymus
34	chr12:57398800-57399400	Enhancers	Rectal Mucosa Donor 31	rectum
35	chr12:57398800-57399600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
36	chr12:57398800-57399600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
37	chr12:57398800-57399600	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
38	chr12:57398800-57399600	Enhancers	Primary T killer memory cells from peripheral blood	blood
39	chr12:57398800-57399600	Weak transcription	Sigmoid Colon	Sigmoid Colon
40	chr12:57398800-57399600	Flanking Active TSS	Stomach Smooth Muscle	stomach
41	chr12:57398800-57399800	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
42	chr12:57398800-57399800	Flanking Active TSS	Liver	Liver
43	chr12:57398800-57399800	Flanking Active TSS	Dnd41	blood
44	chr12:57398800-57400000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
45	chr12:57399000-57399400	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
46	chr12:57399000-57399400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
47	chr12:57399000-57399400	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr12:57399000-57399400	Flanking Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
49	chr12:57399000-57399400	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
50	chr12:57399000-57399400	Enhancers	Primary monocytes fromperipheralblood	blood

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