Variant report

Variant	esv3444965
Chromosome Location	chr12:56400510-56402733
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:456)
CpG islands
(count:244)
Chromatin interactive
region (count:29)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:456 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:56400977-56401233	K562	blood:	n/a	n/a
2	ARID3A	chr12:56400846-56401258	HepG2	liver:	n/a	n/a
3	ATF2	chr12:56400778-56401316	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr12:56400778-56401261	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr12:56400920-56401388	GM12878	blood:	n/a	n/a
6	ATF2	chr12:56400994-56401325	GM12878	blood:	n/a	n/a
7	BCL3	chr12:56400657-56401310	A549	lung:	n/a	chr12:56401226-56401235
8	BCL3	chr12:56400637-56401448	A549	lung:	n/a	chr12:56401435-56401448 chr12:56401434-56401443 chr12:56401226-56401235
9	BCLAF1	chr12:56400912-56401399	GM12878	blood:	n/a	chr12:56401226-56401235
10	BHLHE40	chr12:56400890-56401338	GM12878	blood:	n/a	n/a
11	BHLHE40	chr12:56400825-56401264	K562	blood:	n/a	n/a
12	BRCA1	chr12:56400938-56401264	Hela-S3	cervix:	n/a	n/a
13	CBX3	chr12:56400621-56401340	K562	blood:	n/a	n/a
14	CCNT2	chr12:56400875-56401478	K562	blood:	n/a	chr12:56401240-56401249 chr12:56401435-56401444
15	CEBPD	chr12:56400978-56401542	HepG2	liver:	n/a	n/a
16	CEBPZ	chr12:56401047-56401161	HepG2	liver:	n/a	n/a
17	CHD1	chr12:56401718-56402099	H1-hESC	embryonic stem cell:	n/a	n/a
18	CHD2	chr12:56401905-56402035	GM12878	blood:	n/a	n/a
19	CHD2	chr12:56400986-56401348	GM12878	blood:	n/a	n/a
20	CHD2	chr12:56400966-56401250	HepG2	liver:	n/a	n/a
21	CHD2	chr12:56401805-56401817	HepG2	liver:	n/a	n/a
22	CHD2	chr12:56401003-56401184	K562	blood:	n/a	n/a
23	CHD2	chr12:56400954-56401309	H1-hESC	embryonic stem cell:	n/a	n/a
24	CHD2	chr12:56400864-56401484	Hela-S3	cervix:	n/a	n/a
25	CREB1	chr12:56401085-56401273	A549	lung:	n/a	n/a
26	CREB1	chr12:56400922-56401386	A549	lung:	n/a	n/a
27	CTCF	chr12:56401051-56401205	K562	blood:	n/a	n/a
28	CTCF	chr12:56401131-56401222	Lung_OC	lung:	n/a	n/a
29	CTCF	chr12:56401100-56401250	HVMF	connective:	n/a	n/a
30	CTCF	chr12:56401121-56401248	Pancreas_OC	pancreas:	n/a	n/a
31	CTCF	chr12:56401060-56401210	HCPEpiC	choroid plexus:	n/a	n/a
32	CTCF	chr12:56401100-56401250	AG04449	skin:	n/a	n/a
33	CTCF	chr12:56401080-56401230	HEK293	kidney:	n/a	n/a
34	CTCF	chr12:56401120-56401270	Caco-2	colon:	n/a	n/a
35	CTCF	chr12:56401102-56401230	Spleen_OC	spleen:	n/a	n/a
36	CUX1	chr12:56400900-56401327	GM12878	blood:	n/a	n/a
37	CUX1	chr12:56400907-56401265	K562	blood:	n/a	n/a
38	E2F4	chr12:56400983-56401293	MCF10A-Er-Src	breast:	n/a	chr12:56401105-56401114
39	E2F6	chr12:56401689-56401908	K562	blood:	n/a	n/a
40	E2F6	chr12:56401056-56401246	K562	blood:	n/a	chr12:56401105-56401114
41	E2F6	chr12:56401632-56402027	H1-hESC	embryonic stem cell:	n/a	n/a
42	E2F6	chr12:56401606-56401902	K562	blood:	n/a	n/a
43	EGR1	chr12:56400993-56401285	K562	blood:	n/a	n/a
44	EGR1	chr12:56401426-56401758	GM12878	blood:	n/a	chr12:56401549-56401563 chr12:56401434-56401444 chr12:56401570-56401584 chr12:56401614-56401628 chr12:56401435-56401450 chr12:56401436-56401449 chr12:56401436-56401449 chr12:56401496-56401505
45	EGR1	chr12:56401521-56401752	GM12878	blood:	n/a	chr12:56401549-56401563 chr12:56401570-56401584 chr12:56401614-56401628
46	EGR1	chr12:56401054-56401312	GM12878	blood:	n/a	n/a
47	EGR1	chr12:56401443-56401856	K562	blood:	n/a	chr12:56401549-56401563 chr12:56401570-56401584 chr12:56401614-56401628 chr12:56401496-56401505
48	EGR1	chr12:56401455-56401890	ECC-1	luminal epithelium:	n/a	chr12:56401549-56401563 chr12:56401570-56401584 chr12:56401614-56401628 chr12:56401496-56401505
49	EGR1	chr12:56401361-56401865	K562	blood:	n/a	chr12:56401549-56401563 chr12:56401434-56401444 chr12:56401570-56401584 chr12:56401614-56401628 chr12:56401435-56401450 chr12:56401436-56401449 chr12:56401436-56401449 chr12:56401496-56401505
50	ELF1	chr12:56400979-56401390	SK-N-SH	brain:	n/a	chr12:56401322-56401334

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:56401323-56401373	HCT-116	colon:	n/a
2	chr12:56401370-56401420	HNPCEpiC	eye:	n/a
3	chr12:56401370-56401420	MCF-7	breast:	n/a
4	chr12:56401323-56401373	HCM	heart:	n/a
5	chr12:56401126-56401176	NB4	blood:	n/a
6	chr12:56401126-56401176	K562	blood:	n/a
7	chr12:56401323-56401373	T-47D	breast:	n/a
8	chr12:56401126-56401176	PFSK-1	brain:	n/a
9	chr12:56401370-56401420	AG10803	skin:	n/a
10	chr12:56401806-56401856	GM19239	blood:	n/a
11	chr12:56401323-56401373	U87	brain:	n/a
12	chr12:56401370-56401420	HEEpiC	esophagus:	n/a
13	chr12:56401370-56401420	AG09309	skin:	n/a
14	chr12:56401370-56401420	ovcar-3	ovarian:	n/a
15	chr12:56401806-56401856	Hepatocyte	liver:	n/a
16	chr12:56401126-56401176	AG10803	skin:	n/a
17	chr12:56401806-56401856	HepG2	liver:	n/a
18	chr12:56401323-56401373	Hela-S3	cervix:	n/a
19	chr12:56401126-56401176	SAEC	small airway:	n/a
20	chr12:56401370-56401420	NHDF-neo	bronchial:	n/a
21	chr12:56401126-56401176	HL-60	blood:	n/a
22	chr12:56401806-56401856	ECC-1	luminal epithelium:	n/a
23	chr12:56401370-56401420	Jurkat	blood:	n/a
24	chr12:56401370-56401420	LNCaP	prostate:	n/a
25	chr12:56401370-56401420	AoSMC	blood vessel:	n/a
26	chr12:56401370-56401420	HIPEpiC	eye:	n/a
27	chr12:56401126-56401176	BJ	skin:	n/a
28	chr12:56401370-56401420	MCF10A-Er-Src	breast:	n/a
29	chr12:56401806-56401856	MCF-7	breast:	n/a
30	chr12:56401323-56401373	A549	lung:	n/a
31	chr12:56401126-56401176	SK-N-SH_RA	brain:	n/a
32	chr12:56401370-56401420	HAEpiC	amniotic membrane:	n/a
33	chr12:56401126-56401176	PANC-1	pancreas:	n/a
34	chr12:56401806-56401856	H1-hESC	embryonic stem cell:	embryo
35	chr12:56401370-56401420	BE2_C	brain:	n/a
36	chr12:56401323-56401373	PFSK-1	brain:	n/a
37	chr12:56401806-56401856	IMR90	lung:	fetal
38	chr12:56401806-56401856	GM12878	blood:	n/a
39	chr12:56401806-56401856	HMEC	breast:	n/a
40	chr12:56401370-56401420	PANC-1	pancreas:	n/a
41	chr12:56401126-56401176	ovcar-3	ovarian:	n/a
42	chr12:56401370-56401420	HepG2	liver:	n/a
43	chr12:56401323-56401373	BJ	skin:	n/a
44	chr12:56401126-56401176	GM06990	blood:	n/a
45	chr12:56401126-56401176	Jurkat	blood:	n/a
46	chr12:56401126-56401176	SK-N-MC	brain:	n/a
47	chr12:56401126-56401176	NH-A	brain:	n/a
48	chr12:56401323-56401373	HPAEpiC	pulmonary alveolar:	n/a
49	chr12:56401126-56401176	PrEC	prostate:	n/a
50	chr12:56401126-56401176	HAEpiC	amniotic membrane:	n/a

(count:29 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:56401139..56403498-chr12:56475848..56478502,3	K562	blood:
2	chr12:56390809..56392348-chr12:56401235..56403925,2	K562	blood:
3	chr12:56399990..56402705-chr12:56510349..56512541,3	K562	blood:
4	chr12:56386715..56395273-chr12:56398367..56404356,15	MCF-7	breast:
5	chr12:56399617..56401195-chr12:56518712..56520569,2	K562	blood:
6	chr12:56399898..56405642-chr12:56433175..56438589,7	K562	blood:
7	chr12:56400079..56406275-chr12:56406695..56413732,8	MCF-7	breast:
8	chr12:56399175..56403137-chr12:56403716..56405667,4	MCF-7	breast:
9	chr12:56211633..56216017-chr12:56399885..56403410,4	MCF-7	breast:
10	chr12:56318939..56322802-chr12:56399424..56402892,5	MCF-7	breast:
11	chr12:56364817..56368355-chr12:56399269..56402650,4	K562	blood:
12	chr12:56398950..56401873-chr12:56435306..56438317,7	MCF-7	breast:
13	chr12:56360672..56362289-chr12:56400535..56402399,2	MCF-7	breast:
14	chr12:56388289..56393996-chr12:56394860..56404076,14	K562	blood:
15	chr12:56389364..56393818-chr12:56396293..56409099,19	MCF-7	breast:
16	chr12:56222087..56223926-chr12:56400815..56402785,2	MCF-7	breast:
17	chr12:56400915..56403340-chr12:56510572..56513192,4	MCF-7	breast:
18	chr12:56323623..56326295-chr12:56400061..56402642,2	MCF-7	breast:
19	chr12:56122770..56125786-chr12:56400050..56403264,3	K562	blood:
20	chr12:56399990..56401630-chr12:56510349..56512475,2	K562	blood:
21	chr12:56221928..56223913-chr12:56399026..56401166,2	MCF-7	breast:
22	chr12:56224367..56226323-chr12:56401356..56403743,2	MCF-7	breast:
23	chr12:56399677..56401195-chr12:56518712..56520828,2	K562	blood:
24	chr12:56399605..56402732-chr12:56433705..56437280,6	MCF-7	breast:
25	chr12:56390656..56393336-chr12:56399432..56401234,2	K562	blood:
26	chr12:56398217..56408038-chr12:56433794..56439966,15	K562	blood:
27	chr12:56365318..56368355-chr12:56399244..56401399,3	K562	blood:
28	chr12:56400102..56402586-chr12:56415416..56418384,2	MCF-7	breast:
29	chr12:56326233..56328752-chr12:56399282..56401795,2	MCF-7	breast:

No data

Variant related genes	Relation type
IKZF4	TF binding region
IKZF4	CpG island
ENSG00000123353	chromatin interactions
ENSG00000135404	chromatin interactions
ENSG00000139641	chromatin interactions
ENSG00000170473	chromatin interactions
ENSG00000258056	chromatin interactions
ENSG00000257449	chromatin interactions
ENSG00000258554	chromatin interactions
ENSG00000123411	chromatin interactions
ENSG00000229117	chromatin interactions
ENSG00000065357	chromatin interactions
ENSG00000182796	chromatin interactions
ENSG00000197728	chromatin interactions
ENSG00000135392	chromatin interactions
ENSG00000123374	chromatin interactions
ENSG00000065361	chromatin interactions
ENSG00000135482	chromatin interactions
ENSG00000111540	chromatin interactions
ENSG00000185664	chromatin interactions
ENSG00000139531	chromatin interactions

Extended variants
information (count: 63 )
Associated
traits (count: 88 )

Variant overlapped rSNPs/rCNVs (count:63 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs573008607	chr12:56400511-56400512	Weak transcription Enhancers	Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
2	rs181808740	chr12:56400529-56400530	Weak transcription Enhancers	TF binding region Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
3	rs28756688	chr12:56400580-56400581	Weak transcription Enhancers	TF binding region Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
4	rs142581472	chr12:56400600-56400601	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
5	rs562888163	chr12:56400615-56400616	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
6	rs561711075	chr12:56400631-56400632	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
7	rs528882012	chr12:56400730-56400731	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
8	rs186044721	chr12:56400753-56400754	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
9	rs367618065	chr12:56400772-56400773	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
10	rs371406970	chr12:56400821-56400822	Active TSS Flanking Active TSS Enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
11	rs112253752	chr12:56400840-56400841	Active TSS Flanking Active TSS Enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
12	rs576641161	chr12:56400858-56400859	Active TSS Flanking Active TSS Enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
13	rs374860846	chr12:56400916-56400917	Active TSS Flanking Active TSS Enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
14	rs190457294	chr12:56400921-56400922	Active TSS Flanking Active TSS Enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
15	rs141635677	chr12:56400933-56400934	Active TSS Flanking Active TSS Enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
16	rs566710535	chr12:56400956-56400957	Active TSS Flanking Active TSS Enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
17	rs181628807	chr12:56401017-56401018	Active TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
18	rs549064643	chr12:56401063-56401064	Active TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
19	rs10876864	chr12:56401085-56401086	Active TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	19 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance disease
20	rs186351985	chr12:56401167-56401168	Active TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	20 gene(s)	Overlapped CNVs	n/a
21	rs556250055	chr12:56401241-56401242	Active TSS Transcr. at gene 5' and 3' Weak transcription Enhancers	TF binding region Chromatin interactive region	20 gene(s)	Overlapped CNVs	n/a
22	rs530377394	chr12:56401261-56401262	Active TSS Transcr. at gene 5' and 3' Weak transcription Enhancers	TF binding region Chromatin interactive region	20 gene(s)	Overlapped CNVs	n/a
23	rs191302528	chr12:56401262-56401263	Active TSS Transcr. at gene 5' and 3' Weak transcription Enhancers	TF binding region Chromatin interactive region	20 gene(s)	Overlapped CNVs	n/a
24	rs532964291	chr12:56401268-56401269	Active TSS Transcr. at gene 5' and 3' Weak transcription Enhancers	TF binding region Chromatin interactive region	20 gene(s)	Overlapped CNVs	n/a
25	rs539727960	chr12:56401276-56401277	Active TSS Transcr. at gene 5' and 3' Weak transcription Enhancers	TF binding region Chromatin interactive region	20 gene(s)	Overlapped CNVs	n/a
26	rs558023234	chr12:56401336-56401337	Active TSS Transcr. at gene 5' and 3' Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	20 gene(s)	Overlapped CNVs	n/a
27	rs71446524	chr12:56401541-56401542	Active TSS Transcr. at gene 5' and 3' Weak transcription Enhancers	TF binding region Chromatin interactive region	20 gene(s)	Overlapped CNVs	n/a
28	rs573070050	chr12:56401602-56401603	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	20 gene(s)	Overlapped CNVs	n/a
29	rs540380046	chr12:56401608-56401609	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	20 gene(s)	Overlapped CNVs	n/a
30	rs371907142	chr12:56401616-56401617	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	20 gene(s)	Overlapped CNVs	n/a
31	rs375227437	chr12:56401618-56401619	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	20 gene(s)	Overlapped CNVs	n/a
32	rs35016893	chr12:56401634-56401635	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	20 gene(s)	Overlapped CNVs	n/a
33	rs145495590	chr12:56401684-56401685	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	20 gene(s)	Overlapped CNVs	n/a
34	rs546707530	chr12:56401767-56401768	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	20 gene(s)	Overlapped CNVs	n/a
35	rs573618206	chr12:56401771-56401772	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	20 gene(s)	Overlapped CNVs	n/a
36	rs116686330	chr12:56401887-56401888	Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	20 gene(s)	Overlapped CNVs	n/a
37	rs562325046	chr12:56401980-56401981	Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	20 gene(s)	Overlapped CNVs	n/a
38	rs533716590	chr12:56402007-56402008	Flanking Active TSS Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	20 gene(s)	Overlapped CNVs	n/a
39	rs182622452	chr12:56402085-56402086	Flanking Active TSS Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	20 gene(s)	Overlapped CNVs	n/a
40	rs560363370	chr12:56402108-56402109	Flanking Active TSS Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	20 gene(s)	Overlapped CNVs	n/a
41	rs78439475	chr12:56402125-56402126	Flanking Active TSS Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	20 gene(s)	Overlapped CNVs	n/a
42	rs186719671	chr12:56402135-56402136	Flanking Active TSS Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	20 gene(s)	Overlapped CNVs	n/a
43	rs567763984	chr12:56402159-56402160	Flanking Active TSS Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	20 gene(s)	Overlapped CNVs	n/a
44	rs531689811	chr12:56402163-56402164	Flanking Active TSS Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	20 gene(s)	Overlapped CNVs	n/a
45	rs1701706	chr12:56402204-56402205	Flanking Active TSS Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	20 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
46	rs549129226	chr12:56402232-56402233	Flanking Active TSS Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	20 gene(s)	Overlapped CNVs	n/a
47	rs191225461	chr12:56402283-56402284	Flanking Active TSS Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	20 gene(s)	Overlapped CNVs	n/a
48	rs572378124	chr12:56402307-56402308	Flanking Active TSS Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	20 gene(s)	Overlapped CNVs	n/a
49	rs568982946	chr12:56402333-56402334	Flanking Active TSS Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	20 gene(s)	Overlapped CNVs	n/a
50	rs550867749	chr12:56402455-56402456	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:88)

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
low-grade B-cell lymphoma tumor	18367492	CNVD
Breast cancer	21785460	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	18179710	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	20531469	CNVD
Multiple myeloma	16616336	CNVD
Rhabdomyosarcoma	16790082	CNVD
Renal cell carcinoma	18765545	CNVD
Urothelial cell carcinoma	18451213	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	21138945	CNVD
Glioblastoma multiforme	21569311	CNVD
Glioblastoma multiforme	19115005	CNVD
Glioblastoma multiforme	21390271	CNVD
Cancer	20164919	CNVD
Breast cancer	21509527	CNVD
Lung adenocarcinoma	17982442	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
Liposarcoma	21253554	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:574 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:56391600-56400800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
2	chr12:56391800-56400600	Weak transcription	Muscle Satellite Cultured Cells	--
3	chr12:56391800-56400600	Weak transcription	NHEK	skin
4	chr12:56392000-56400600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr12:56392000-56400600	Weak transcription	Fetal Thymus	thymus
6	chr12:56392000-56400600	Weak transcription	Right Atrium	heart
7	chr12:56392000-56400600	Weak transcription	HMEC	breast
8	chr12:56392000-56400800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
9	chr12:56392000-56400800	Weak transcription	GM12878-XiMat	blood
10	chr12:56392400-56400800	Weak transcription	Fetal Brain Male	brain
11	chr12:56396000-56400600	Weak transcription	Fetal Kidney	kidney
12	chr12:56396200-56400600	Weak transcription	Brain Germinal Matrix	brain
13	chr12:56396200-56400600	Weak transcription	Rectal Mucosa Donor 31	rectum
14	chr12:56397000-56400600	Weak transcription	NH-A	brain
15	chr12:56398000-56400600	Weak transcription	HSMM	muscle
16	chr12:56398200-56400600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
17	chr12:56398200-56400600	Weak transcription	Esophagus	oesophagus
18	chr12:56398400-56400600	Weak transcription	H1 Cell Line	embryonic stem cell
19	chr12:56398400-56400600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
20	chr12:56398400-56400600	Weak transcription	Colon Smooth Muscle	Colon
21	chr12:56398400-56400600	Weak transcription	Monocytes-CD14+_RO01746	blood
22	chr12:56398400-56400800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
23	chr12:56398400-56400800	Weak transcription	Aorta	Aorta
24	chr12:56398600-56400600	Weak transcription	H9 Cell Line	embryonic stem cell
25	chr12:56398600-56400600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr12:56398600-56400600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
27	chr12:56398600-56400600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
28	chr12:56398600-56400600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
29	chr12:56398600-56400600	Weak transcription	Duodenum Smooth Muscle	Duodenum
30	chr12:56398600-56400600	Weak transcription	Left Ventricle	heart
31	chr12:56398600-56400600	Weak transcription	Rectal Mucosa Donor 29	rectum
32	chr12:56398600-56400600	Weak transcription	A549	lung
33	chr12:56398600-56400600	Weak transcription	Osteobl	bone
34	chr12:56398800-56400600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
35	chr12:56398800-56400600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
36	chr12:56398800-56400600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
37	chr12:56398800-56400600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
38	chr12:56398800-56400600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
39	chr12:56398800-56400600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
40	chr12:56398800-56400600	Weak transcription	Lung	lung
41	chr12:56398800-56400600	Weak transcription	Rectal Smooth Muscle	rectum
42	chr12:56398800-56400600	Weak transcription	Right Ventricle	heart
43	chr12:56398800-56400600	Weak transcription	Skeletal Muscle Male	skeletal muscle
44	chr12:56398800-56400600	Weak transcription	Skeletal Muscle Female	skeletal muscle
45	chr12:56398800-56400600	Enhancers	HepG2	liver
46	chr12:56398800-56400600	Weak transcription	NHLF	lung
47	chr12:56398800-56400800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
48	chr12:56398800-56400800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
49	chr12:56398800-56400800	Weak transcription	Gastric	stomach
50	chr12:56398800-56400800	Weak transcription	Ovary	ovary

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