Variant report

Variant	esv275479
Chromosome Location	chr12:56478324-56481063
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:259)
CpG islands
(count:123)
Chromatin interactive
region (count:17)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:259 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BHLHE40	chr12:56479096-56479109	K562	blood:	n/a	n/a
2	CBX3	chr12:56478961-56479287	K562	blood:	n/a	n/a
3	CREB1	chr12:56478929-56479205	A549	lung:	n/a	n/a
4	CTCF	chr12:56479018-56479244	Medullo	brain:	n/a	n/a
5	CTCF	chr12:56479040-56479190	NB4	blood:	n/a	n/a
6	CTCF	chr12:56479040-56479190	HPF	lung:	n/a	n/a
7	CTCF	chr12:56478714-56479451	A549	lung:	n/a	n/a
8	CTCF	chr12:56479060-56479210	GM12875	blood:	n/a	n/a
9	CTCF	chr12:56479040-56479190	HFF-Myc	foreskin:	n/a	n/a
10	CTCF	chr12:56479069-56479205	GM10248	blood:	n/a	n/a
11	CTCF	chr12:56479040-56479190	AoAF	blood vessel:	n/a	n/a
12	CTCF	chr12:56479040-56479190	HPAF	blood vessel:	n/a	n/a
13	CTCF	chr12:56479060-56479210	HVMF	connective:	n/a	n/a
14	CTCF	chr12:56479025-56479234	Gliobla	brain:	n/a	n/a
15	CTCF	chr12:56478956-56479295	GM12878	blood:	n/a	n/a
16	CTCF	chr12:56479060-56479210	HCT-116	colon:	n/a	n/a
17	CTCF	chr12:56479020-56479170	GM12873	blood:	n/a	n/a
18	CTCF	chr12:56479040-56479190	WI-38	lung:	n/a	n/a
19	CTCF	chr12:56478782-56478875	GM10266	blood:	n/a	n/a
20	CTCF	chr12:56479025-56479221	HepG2	liver:	n/a	n/a
21	CTCF	chr12:56478640-56478790	GM12870	blood:	n/a	n/a
22	CTCF	chr12:56479080-56479230	AoAF	blood vessel:	n/a	n/a
23	CTCF	chr12:56479120-56479270	NHLF	lung:	n/a	n/a
24	CTCF	chr12:56478838-56478871	GM12878	blood:	n/a	n/a
25	CTCF	chr12:56479022-56479241	Hela-S3	cervix:	n/a	n/a
26	CTCF	chr12:56479020-56479170	SK-N-SH_RA	brain:	n/a	n/a
27	CTCF	chr12:56478929-56479242	HepG2	liver:	n/a	n/a
28	CTCF	chr12:56479080-56479230	HRPEpiC	eye:	n/a	n/a
29	CTCF	chr12:56479008-56479218	HepG2	liver:	n/a	n/a
30	CTCF	chr12:56479060-56479210	HRPEpiC	eye:	n/a	n/a
31	CTCF	chr12:56479060-56479210	HPAF	blood vessel:	n/a	n/a
32	CTCF	chr12:56479000-56479150	GM12801	blood:	n/a	n/a
33	CTCF	chr12:56479055-56479214	MCF-7	breast:	n/a	n/a
34	CTCF	chr12:56479060-56479210	HCFaa	heart:	n/a	n/a
35	CTCF	chr12:56479100-56479250	GM12864	blood:	n/a	n/a
36	CTCF	chr12:56478784-56478829	K562	blood:	n/a	n/a
37	CTCF	chr12:56479080-56479230	SAEC	small airway:	n/a	n/a
38	CTCF	chr12:56479036-56479235	GM19239	blood:	n/a	n/a
39	CTCF	chr12:56479080-56479230	AG04449	skin:	n/a	n/a
40	CTCF	chr12:56479080-56479230	GM12870	blood:	n/a	n/a
41	CTCF	chr12:56479020-56479170	NHEK	skin:	n/a	n/a
42	CTCF	chr12:56479039-56479213	GM10266	blood:	n/a	n/a
43	CTCF	chr12:56479100-56479250	WI-38	lung:	n/a	n/a
44	CTCF	chr12:56478953-56479317	K562	blood:	n/a	n/a
45	CTCF	chr12:56479040-56479190	GM12875	blood:	n/a	n/a
46	CTCF	chr12:56478965-56479235	SK-N-SH_RA	brain:	n/a	n/a
47	CTCF	chr12:56479080-56479230	HCT-116	colon:	n/a	n/a
48	CTCF	chr12:56478863-56479310	SK-N-SH	brain:	n/a	n/a
49	CTCF	chr12:56478908-56479253	GM12891	blood:	n/a	n/a
50	CTCF	chr12:56478978-56479263	GM19238	blood:	n/a	n/a

(count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:56478329-56478379	U87	brain:	n/a
2	chr12:56478329-56478379	U87	brain:	n/a
3	chr12:56478329-56478379	SKMC	muscle:	n/a
4	chr12:56479243-56479293	NHDF-neo	bronchial:	n/a
5	chr12:56479243-56479293	HMEC	breast:	n/a
6	chr12:56478329-56478379	PANC-1	pancreas:	n/a
7	chr12:56479243-56479293	LNCaP	prostate:	n/a
8	chr12:56479243-56479293	SKMC	muscle:	n/a
9	chr12:56478329-56478379	HRE	kidney:	n/a
10	chr12:56479243-56479293	MCF-7	breast:	n/a
11	chr12:56478329-56478379	HL-60	blood:	n/a
12	chr12:56478329-56478379	SK-N-SH_RA	brain:	n/a
13	chr12:56479243-56479293	AG04449	skin:	fetal
14	chr12:56479243-56479293	AG10803	skin:	n/a
15	chr12:56478329-56478379	NT2-D1	testis:	n/a
16	chr12:56478329-56478379	CMK	blood:	n/a
17	chr12:56479243-56479293	Hela-S3	cervix:	n/a
18	chr12:56479243-56479293	PANC-1	pancreas:	n/a
19	chr12:56479243-56479293	GM12891	blood:	n/a
20	chr12:56479243-56479293	A549	lung:	n/a
21	chr12:56478329-56478379	SAEC	small airway:	n/a
22	chr12:56478329-56478379	BE2_C	brain:	n/a
23	chr12:56479243-56479293	RPTEC	kidney:	n/a
24	chr12:56479243-56479293	HUVEC	blood vessel:	n/a
25	chr12:56478329-56478379	Hela-S3	cervix:	n/a
26	chr12:56479243-56479293	NT2-D1	testis:	n/a
27	chr12:56479243-56479293	GM12892	blood:	n/a
28	chr12:56479243-56479293	SK-N-SH	brain:	n/a
29	chr12:56478329-56478379	HUVEC	blood vessel:	n/a
30	chr12:56479243-56479293	ECC-1	luminal epithelium:	n/a
31	chr12:56478329-56478379	AG04450	lung:	fetal
32	chr12:56479243-56479293	HRPEpiC	eye:	n/a
33	chr12:56479243-56479293	T-47D	breast:	n/a
34	chr12:56478329-56478379	T-47D	breast:	n/a
35	chr12:56478329-56478379	MCF10A-Er-Src	breast:	n/a
36	chr12:56479243-56479293	SAEC	small airway:	n/a
37	chr12:56478329-56478379	HRCEpiC	kidney:	n/a
38	chr12:56478329-56478379	PrEC	prostate:	n/a
39	chr12:56478329-56478379	HCM	heart:	n/a
40	chr12:56479243-56479293	AoSMC	blood vessel:	n/a
41	chr12:56479243-56479293	ProgFib	skin:	n/a
42	chr12:56479243-56479293	NHBE	bronchial:	n/a
43	chr12:56478329-56478379	HEEpiC	esophagus:	n/a
44	chr12:56479243-56479293	HRE	kidney:	n/a
45	chr12:56478329-56478379	GM12891	blood:	n/a
46	chr12:56478329-56478379	AG09319	gingival:	n/a
47	chr12:56479243-56479293	HCPEpiC	choroid plexus:	n/a
48	chr12:56479243-56479293	PFSK-1	brain:	n/a
49	chr12:56478329-56478379	BJ	skin:	n/a
50	chr12:56479243-56479293	HNPCEpiC	eye:	n/a

(count:17 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:56470948..56480058-chr12:56507665..56513741,17	K562	blood:
2	chr12:56471261..56483436-chr12:56494778..56506435,58	MCF-7	breast:
3	chr12:56401139..56403498-chr12:56475848..56478502,3	K562	blood:
4	chr12:56480948..56483944-chr12:56582412..56584224,2	MCF-7	breast:
5	chr12:56472058..56475455-chr12:56477194..56480758,7	K562	blood:
6	chr12:56475818..56478694-chr12:56550865..56553540,2	MCF-7	breast:
7	chr12:56471198..56482935-chr12:56506922..56516262,73	MCF-7	breast:
8	chr12:56434874..56437408-chr12:56478548..56481298,5	MCF-7	breast:
9	chr12:56472197..56476808-chr12:56477200..56483474,8	K562	blood:
10	chr12:56479547..56482391-chr12:56486376..56489009,4	MCF-7	breast:
11	chr12:56478670..56479606-chr12:56519593..56520546,2	K562	blood:
12	chr12:56475587..56477681-chr12:56479959..56483381,3	K562	blood:
13	chr12:56477785..56480732-chr12:56480999..56482535,2	K562	blood:
14	chr12:56480457..56482671-chr12:56551431..56553649,2	MCF-7	breast:
15	chr12:56477888..56479388-chr19:35606832..35608694,2	MCF-7	breast:
16	chr12:56477785..56480732-chr12:56480999..56482535,2	K562	blood:
17	chr12:56435284..56441183-chr12:56476886..56481327,8	MCF-7	breast:

No data

Variant related genes	Relation type
ERBB3	TF binding region
ERBB3	CpG island
ENSG00000257449	chromatin interactions
ENSG00000092841	chromatin interactions
ENSG00000229117	chromatin interactions
ENSG00000139613	chromatin interactions
ENSG00000170515	chromatin interactions
ENSG00000089356	chromatin interactions
ENSG00000197728	chromatin interactions
ENSG00000135482	chromatin interactions
ENSG00000196465	chromatin interactions
ENSG00000258199	chromatin interactions
ENSG00000257809	chromatin interactions
ENSG00000258345	chromatin interactions
ENSG00000257553	chromatin interactions
ENSG00000139641	chromatin interactions
ENSG00000123411	chromatin interactions
ENSG00000065361	chromatin interactions
ENSG00000257411	chromatin interactions

Extended variants
information (count: 131 )
Associated
traits (count: 89 )

Variant overlapped rSNPs/rCNVs (count:131 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs555359169	chr12:56478329-56478330	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region CpG island Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
2	rs568319076	chr12:56478330-56478331	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region CpG island Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
3	rs368891812	chr12:56478342-56478343	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region CpG island Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
4	rs550941832	chr12:56478357-56478358	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region CpG island Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
5	rs35810389	chr12:56478382-56478383	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
6	rs386376616	chr12:56478383-56478384	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
7	rs386376617	chr12:56478396-56478397	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
8	rs71074898	chr12:56478397-56478398	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
9	rs570057511	chr12:56478495-56478496	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
10	rs531574760	chr12:56478535-56478536	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
11	rs558990919	chr12:56478592-56478593	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
12	rs12817471	chr12:56478607-56478608	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	15 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
13	rs535186970	chr12:56478613-56478614	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
14	rs74928813	chr12:56478614-56478615	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
15	rs574735703	chr12:56478620-56478621	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
16	rs542106370	chr12:56478627-56478628	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
17	rs544290150	chr12:56478628-56478629	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
18	rs574868480	chr12:56478655-56478656	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
19	rs7971751	chr12:56478658-56478659	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	15 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
20	rs73338402	chr12:56478682-56478683	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	15 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs77830169	chr12:56478684-56478685	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
22	rs528182386	chr12:56478688-56478689	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
23	rs112675254	chr12:56478697-56478698	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
24	rs201378576	chr12:56478802-56478803	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Enhancers	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
25	rs77228285	chr12:56478809-56478810	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Enhancers	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
26	rs200856864	chr12:56478830-56478831	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Enhancers	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
27	rs201479792	chr12:56478846-56478847	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Enhancers	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
28	rs142358877	chr12:56478850-56478851	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Enhancers	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
29	rs146486757	chr12:56478851-56478852	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Enhancers	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
30	rs984896	chr12:56478858-56478859	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Enhancers	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
31	rs185577186	chr12:56478859-56478860	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Enhancers	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
32	rs375644422	chr12:56478881-56478882	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Enhancers	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
33	rs569206705	chr12:56478938-56478939	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Enhancers	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
34	rs540018426	chr12:56478942-56478943	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Enhancers	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
35	rs369698449	chr12:56478958-56478959	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Enhancers	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
36	rs373473538	chr12:56478964-56478965	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Enhancers	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
37	rs537427649	chr12:56479003-56479004	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
38	rs199586304	chr12:56479008-56479009	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
39	rs368815108	chr12:56479011-56479012	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
40	rs552306307	chr12:56479054-56479055	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
41	rs188955993	chr12:56479088-56479089	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
42	rs372736362	chr12:56479094-56479095	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
43	rs534803783	chr12:56479106-56479107	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
44	rs553090262	chr12:56479108-56479109	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
45	rs548496368	chr12:56479125-56479126	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
46	rs559937373	chr12:56479130-56479131	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
47	rs552597623	chr12:56479201-56479202	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
48	rs79581177	chr12:56479214-56479215	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
49	rs148655905	chr12:56479243-56479244	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region CpG island Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
50	rs548907427	chr12:56479244-56479245	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region CpG island Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:89)

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
Cancer	20164920	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:158 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:56474400-56497200	Weak transcription	Right Atrium	heart
2	chr12:56474600-56478800	Weak transcription	Left Ventricle	heart
3	chr12:56474800-56479800	Weak transcription	HMEC	breast
4	chr12:56475000-56485600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
5	chr12:56475200-56478800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
6	chr12:56475800-56479200	Genic enhancers	ES-UCSF4 Cell Line	embryonic stem cell
7	chr12:56475800-56482400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
8	chr12:56476000-56480000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr12:56476000-56481000	Weak transcription	Spleen	Spleen
10	chr12:56476000-56481800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
11	chr12:56476200-56497200	Weak transcription	Fetal Kidney	kidney
12	chr12:56476400-56478400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
13	chr12:56476400-56480000	Weak transcription	Fetal Heart	heart
14	chr12:56476400-56480200	Weak transcription	Hela-S3	cervix
15	chr12:56476400-56483200	Strong transcription	H9 Cell Line	embryonic stem cell
16	chr12:56476600-56478800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr12:56476600-56479200	Genic enhancers	Fetal Muscle Leg	muscle
18	chr12:56476600-56480400	Weak transcription	A549	lung
19	chr12:56476600-56487400	Weak transcription	Lung	lung
20	chr12:56476600-56496400	Strong transcription	iPS-20b Cell Line	embryonic stem cell
21	chr12:56476600-56497600	Weak transcription	Small Intestine	intestine
22	chr12:56476800-56478600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
23	chr12:56476800-56479000	Weak transcription	Fetal Muscle Trunk	muscle
24	chr12:56476800-56479800	Weak transcription	HSMMtube	muscle
25	chr12:56476800-56487200	Weak transcription	Duodenum Smooth Muscle	Duodenum
26	chr12:56477000-56479800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
27	chr12:56477000-56497000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
28	chr12:56477000-56497000	Strong transcription	HUES48 Cell Line	embryonic stem cell
29	chr12:56477200-56478800	Weak transcription	K562	blood
30	chr12:56477200-56481600	Genic enhancers	Rectal Mucosa Donor 31	rectum
31	chr12:56477400-56479200	Genic enhancers	Pancreas	Pancrea
32	chr12:56477600-56480000	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
33	chr12:56477600-56496600	Strong transcription	HUES64 Cell Line	embryonic stem cell
34	chr12:56477800-56478600	Weak transcription	Placenta	Placenta
35	chr12:56477800-56478800	Enhancers	Brain Substantia Nigra	brain
36	chr12:56477800-56478800	Weak transcription	Esophagus	oesophagus
37	chr12:56477800-56478800	Weak transcription	Placenta Amnion	Placenta Amnion
38	chr12:56477800-56478800	Weak transcription	Rectal Smooth Muscle	rectum
39	chr12:56477800-56478800	Weak transcription	NHEK	skin
40	chr12:56477800-56479200	Genic enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
41	chr12:56477800-56479200	Genic enhancers	Gastric	stomach
42	chr12:56477800-56479400	Genic enhancers	Fetal Intestine Large	intestine
43	chr12:56477800-56479400	Genic enhancers	Fetal Intestine Small	intestine
44	chr12:56477800-56481400	Genic enhancers	Duodenum Mucosa	Duodenum
45	chr12:56477800-56481600	Genic enhancers	Liver	Liver
46	chr12:56477800-56481600	Genic enhancers	Rectal Mucosa Donor 29	rectum
47	chr12:56477800-56485800	Strong transcription	Fetal Stomach	stomach
48	chr12:56477800-56496200	Strong transcription	H1 Cell Line	embryonic stem cell
49	chr12:56478000-56478400	Weak transcription	Sigmoid Colon	Sigmoid Colon
50	chr12:56478000-56478600	Weak transcription	HUES6 Cell Line	embryonic stem cell

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