Variant report

Variant	esv3415547
Chromosome Location	chr8:124420820-124444289
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:924)
CpG islands
(count:915)
Chromatin interactive
region (count:51)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:924 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:124428993-124429007	K562	blood:	n/a	n/a
2	ARID3A	chr8:124428372-124428665	K562	blood:	n/a	n/a
3	ARID3A	chr8:124426174-124426374	HepG2	liver:	n/a	n/a
4	ARID3A	chr8:124429243-124429820	HepG2	liver:	n/a	n/a
5	ARID3A	chr8:124428329-124428737	HepG2	liver:	n/a	n/a
6	ATF1	chr8:124425210-124425470	K562	blood:	n/a	n/a
7	BACH1	chr8:124428987-124429108	K562	blood:	n/a	n/a
8	BACH1	chr8:124428910-124429536	H1-hESC	embryonic stem cell:	n/a	n/a
9	BCL3	chr8:124428840-124429584	A549	lung:	n/a	chr8:124429179-124429192
10	BCLAF1	chr8:124428900-124429296	GM12878	blood:	n/a	chr8:124429179-124429192
11	BHLHE40	chr8:124429827-124430025	K562	blood:	n/a	n/a
12	BHLHE40	chr8:124428438-124429548	K562	blood:	n/a	chr8:124428647-124428663
13	BHLHE40	chr8:124428317-124429690	GM12878	blood:	n/a	chr8:124428647-124428663
14	BHLHE40	chr8:124425183-124425211	K562	blood:	n/a	n/a
15	BRCA1	chr8:124429091-124429496	Hela-S3	cervix:	n/a	n/a
16	BRCA1	chr8:124428409-124428587	HepG2	liver:	n/a	n/a
17	BRCA1	chr8:124429118-124429415	GM12878	blood:	n/a	n/a
18	BRCA1	chr8:124428293-124428885	Hela-S3	cervix:	n/a	n/a
19	BRCA1	chr8:124428436-124428547	GM12878	blood:	n/a	n/a
20	CBX3	chr8:124428247-124429603	K562	blood:	n/a	n/a
21	CCNT2	chr8:124428344-124429402	K562	blood:	n/a	chr8:124428645-124428654
22	CEBPB	chr8:124437249-124437399	HepG2	liver:	n/a	n/a
23	CEBPB	chr8:124437293-124437311	IMR90	lung:	n/a	n/a
24	CEBPB	chr8:124426114-124426472	K562	blood:	n/a	chr8:124426207-124426218 chr8:124426282-124426293
25	CEBPB	chr8:124426205-124426342	HepG2	liver:	n/a	chr8:124426207-124426218 chr8:124426282-124426293
26	CEBPB	chr8:124426097-124426636	HepG2	liver:	n/a	chr8:124426207-124426218 chr8:124426282-124426293
27	CEBPB	chr8:124426204-124426379	K562	blood:	n/a	chr8:124426207-124426218 chr8:124426282-124426293
28	CEBPB	chr8:124426206-124426444	IMR90	lung:	n/a	chr8:124426207-124426218 chr8:124426282-124426293
29	CEBPB	chr8:124428435-124429494	Hela-S3	cervix:	n/a	n/a
30	CEBPB	chr8:124426101-124426469	K562	blood:	n/a	chr8:124426207-124426218 chr8:124426282-124426293
31	CEBPB	chr8:124426063-124426649	HepG2	liver:	n/a	chr8:124426207-124426218 chr8:124426282-124426293
32	CEBPD	chr8:124428817-124429411	HepG2	liver:	n/a	n/a
33	CHD1	chr8:124428942-124429888	H1-hESC	embryonic stem cell:	n/a	n/a
34	CHD1	chr8:124428303-124428618	GM12878	blood:	n/a	n/a
35	CHD2	chr8:124428407-124429546	Hela-S3	cervix:	n/a	n/a
36	CHD2	chr8:124429918-124430078	HepG2	liver:	n/a	n/a
37	CHD2	chr8:124429024-124429379	HepG2	liver:	n/a	n/a
38	CHD2	chr8:124428404-124429853	GM12878	blood:	n/a	n/a
39	CHD2	chr8:124428368-124428555	K562	blood:	n/a	n/a
40	CHD2	chr8:124429667-124429717	K562	blood:	n/a	n/a
41	CHD2	chr8:124428407-124428561	HepG2	liver:	n/a	n/a
42	CHD2	chr8:124428889-124429452	H1-hESC	embryonic stem cell:	n/a	n/a
43	CHD2	chr8:124428836-124429171	K562	blood:	n/a	n/a
44	CREB1	chr8:124428432-124429479	A549	lung:	n/a	n/a
45	CREB1	chr8:124428260-124429580	HepG2	liver:	n/a	n/a
46	CREB1	chr8:124428477-124429479	GM12878	blood:	n/a	n/a
47	CTCF	chr8:124428380-124428530	HAc	cerebellar:	n/a	n/a
48	CTCF	chr8:124428384-124428739	HepG2	liver:	n/a	n/a
49	CTCF	chr8:124428620-124428770	AG04450	lung:	n/a	n/a
50	CTCF	chr8:124429200-124429350	GM12878	blood:	n/a	n/a

(count:915 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:124423501-124423551	AoSMC	blood vessel:	n/a
2	chr8:124428910-124428960	Caco-2	colon:	n/a
3	chr8:124429792-124429842	HCT-116	colon:	n/a
4	chr8:124431781-124431831	AG04450	lung:	fetal
5	chr8:124423636-124423686	HCM	heart:	n/a
6	chr8:124428885-124428935	MCF-7	breast:	n/a
7	chr8:124428640-124428690	HCM	heart:	n/a
8	chr8:124425615-124425665	NB4	blood:	n/a
9	chr8:124423636-124423686	RPTEC	kidney:	n/a
10	chr8:124428640-124428690	PANC-1	pancreas:	n/a
11	chr8:124422995-124423045	U87	brain:	n/a
12	chr8:124425615-124425665	NHBE	bronchial:	n/a
13	chr8:124429792-124429842	HRPEpiC	eye:	n/a
14	chr8:124428803-124428853	HRCEpiC	kidney:	n/a
15	chr8:124428910-124428960	Hepatocyte	liver:	n/a
16	chr8:124423501-124423551	NHDF-neo	bronchial:	n/a
17	chr8:124428803-124428853	U87	brain:	n/a
18	chr8:124442302-124442352	AG09319	gingival:	n/a
19	chr8:124423636-124423686	GM19239	blood:	n/a
20	chr8:124428885-124428935	BE2_C	brain:	n/a
21	chr8:124442302-124442352	RPTEC	kidney:	n/a
22	chr8:124425615-124425665	H1-hESC	embryonic stem cell:	embryo
23	chr8:124423636-124423686	HEEpiC	esophagus:	n/a
24	chr8:124428885-124428935	AG04449	skin:	fetal
25	chr8:124431781-124431831	GM12892	blood:	n/a
26	chr8:124423501-124423551	GM19239	blood:	n/a
27	chr8:124428640-124428690	HMEC	breast:	n/a
28	chr8:124428674-124428724	AG04449	skin:	fetal
29	chr8:124428910-124428960	NHBE	bronchial:	n/a
30	chr8:124428885-124428935	GM12891	blood:	n/a
31	chr8:124428640-124428690	PFSK-1	brain:	n/a
32	chr8:124428640-124428690	MCF-7	breast:	n/a
33	chr8:124423636-124423686	HNPCEpiC	eye:	n/a
34	chr8:124423636-124423686	SK-N-MC	brain:	n/a
35	chr8:124425615-124425665	AG04449	skin:	fetal
36	chr8:124429792-124429842	HEK293	kidney:	embryo
37	chr8:124428540-124428590	MCF-7	breast:	n/a
38	chr8:124442302-124442352	SK-N-SH_RA	brain:	n/a
39	chr8:124429188-124429238	SK-N-SH_RA	brain:	n/a
40	chr8:124423636-124423686	Caco-2	colon:	n/a
41	chr8:124431781-124431831	HUVEC	blood vessel:	n/a
42	chr8:124429417-124429467	HRE	kidney:	n/a
43	chr8:124423501-124423551	HL-60	blood:	n/a
44	chr8:124429792-124429842	T-47D	breast:	n/a
45	chr8:124428640-124428690	HUVEC	blood vessel:	n/a
46	chr8:124429417-124429467	NHDF-neo	bronchial:	n/a
47	chr8:124431781-124431831	NT2-D1	testis:	n/a
48	chr8:124429417-124429467	AG10803	skin:	n/a
49	chr8:124423636-124423686	AoSMC	blood vessel:	n/a
50	chr8:124428540-124428590	GM19239	blood:	n/a

(count:51 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr8:124419214..124422869-chr8:124424403..124427101,4	K562	blood:
2	chr1:108743710..108745219-chr8:124429078..124431227,2	MCF-7	breast:
3	chr8:124285038..124289042-chr8:124427512..124430569,10	MCF-7	breast:
4	chr8:124420257..124422233-chr8:124425540..124427078,2	MCF-7	breast:
5	chr8:124437640..124439225-chr8:124442823..124444649,2	K562	blood:
6	chr8:124428979..124430536-chr8:124438336..124440460,2	MCF-7	breast:
7	chr8:124437876..124440344-chr8:124442670..124445450,2	MCF-7	breast:
8	chr8:124408219..124408941-chr8:124428233..124428961,2	MCF-7	breast:
9	chr8:124253290..124255259-chr8:124427452..124430915,4	MCF-7	breast:
10	chr8:124427993..124430634-chr8:124780278..124783215,3	MCF-7	breast:
11	chr8:124406688..124410730-chr8:124426992..124430866,9	K562	blood:
12	chr8:124443028..124445940-chr8:124779849..124782260,2	MCF-7	breast:
13	chr10:102820879..102821499-chr8:124429095..124429824,2	Hela-S3	cervix:
14	chr8:124416051..124418848-chr8:124419770..124421913,2	MCF-7	breast:
15	chr8:124406056..124410111-chr8:124427174..124433258,8	MCF-7	breast:
16	chr8:124437651..124439233-chr8:124489167..124492093,2	MCF-7	breast:
17	chr8:124442700..124445613-chr8:124461517..124464378,2	K562	blood:
18	chr8:124426263..124428395-chr8:124489396..124491860,2	K562	blood:
19	chr8:124429815..124432313-chr8:124778028..124780178,2	K562	blood:
20	chr8:124428888..124431175-chr8:124432869..124435313,2	MCF-7	breast:
21	chr8:124429705..124433349-chr8:124436919..124438611,3	K562	blood:
22	chr8:124408089..124410281-chr8:124425025..124426733,2	K562	blood:
23	chr8:124428647..124432680-chr8:124438774..124441647,3	K562	blood:
24	chr8:124406999..124409661-chr8:124439973..124442313,3	MCF-7	breast:
25	chr8:124404505..124411576-chr8:124423647..124430734,19	MCF-7	breast:
26	chr8:124405499..124410730-chr8:124426606..124431705,19	K562	blood:
27	chr8:124412641..124414334-chr8:124426914..124428862,2	K562	blood:
28	chr3:63847650..63850355-chr8:124441632..124443283,2	MCF-7	breast:
29	chr8:124287117..124289356-chr8:124428879..124431490,3	MCF-7	breast:
30	chr8:124428532..124430498-chr8:124430799..124434472,3	MCF-7	breast:
31	chr8:124283829..124288838-chr8:124426117..124430573,9	K562	blood:
32	chr17:41150128..41150748-chr8:124428306..124429088,2	Hela-S3	cervix:
33	chr8:124427319..124431344-chr8:124440107..124444172,5	MCF-7	breast:
34	chr8:124402970..124404623-chr8:124425335..124427199,2	K562	blood:
35	chr8:124411247..124413629-chr8:124428301..124430441,2	K562	blood:
36	chr8:124427319..124431344-chr8:124440107..124444172,5	MCF-7	breast:
37	chr8:124430051..124432680-chr8:124438774..124442383,3	K562	blood:
38	chr8:124423744..124425619-chr8:124427989..124430305,2	MCF-7	breast:
39	chr8:124283849..124288367-chr8:124426037..124430184,7	K562	blood:
40	chr8:124437876..124440344-chr8:124442670..124445450,2	MCF-7	breast:
41	chr8:124412329..124414016-chr8:124419223..124421843,2	MCF-7	breast:
42	chr8:124415153..124417409-chr8:124424066..124426465,2	K562	blood:
43	chr8:124427799..124430548-chr8:124432499..124434365,4	K562	blood:
44	chr8:124428346..124430451-chr8:124434801..124437480,2	MCF-7	breast:
45	chr8:124429705..124433349-chr8:124436919..124438611,3	K562	blood:
46	chr8:124435837..124438312-chr8:124449085..124450933,2	MCF-7	breast:
47	chr8:124420257..124422233-chr8:124425540..124427078,2	MCF-7	breast:
48	chr11:62623530..62624100-chr8:124428998..124429986,2	Hela-S3	cervix:
49	chr8:124428663..124430757-chr8:124778757..124780951,2	K562	blood:
50	chr8:124437640..124439225-chr8:124442823..124444649,2	K562	blood:

No data

Variant related genes	Relation type
WDYHV1	TF binding region
ATAD2	TF binding region
WDYHV1	CpG island
ATAD2	CpG island
ENSG00000131469	chromatin interactions
ENSG00000163635	chromatin interactions
ENSG00000156795	chromatin interactions
ENSG00000163634	chromatin interactions
ENSG00000156802	chromatin interactions
ENSG00000165156	chromatin interactions
ENSG00000168003	chromatin interactions
ENSG00000176853	chromatin interactions
ENSG00000189376	chromatin interactions
ENSG00000254294	chromatin interactions

Extended variants
information (count: 1083 )
Associated
traits (count: 144 )

Variant overlapped rSNPs/rCNVs (count:1083 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs370811557	chr8:124420820-124420821	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs545868169	chr8:124420826-124420827	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs182835662	chr8:124420839-124420840	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs112734536	chr8:124420843-124420844	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs111629734	chr8:124420845-124420846	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs4870851	chr8:124420902-124420903	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs529811959	chr8:124420917-124420918	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs368031994	chr8:124421003-124421004	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs550054393	chr8:124421147-124421148	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs543550461	chr8:124421153-124421154	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs140074322	chr8:124421177-124421178	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs112486285	chr8:124421178-124421179	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs146787540	chr8:124421212-124421213	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs565463489	chr8:124421214-124421215	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs140479298	chr8:124421224-124421225	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs554208566	chr8:124421225-124421226	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs71573679	chr8:124421231-124421232	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs4871363	chr8:124421255-124421256	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
19	rs116024965	chr8:124421292-124421293	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs376633496	chr8:124421314-124421315	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs149198820	chr8:124421354-124421355	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs577452847	chr8:124421355-124421356	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs114634488	chr8:124421361-124421362	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs553426259	chr8:124421365-124421366	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs143339659	chr8:124421378-124421379	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs75668541	chr8:124421393-124421394	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs4307325	chr8:124421397-124421398	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
28	rs529948992	chr8:124421412-124421413	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs186753023	chr8:124421471-124421472	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs191463390	chr8:124421475-124421476	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs532280805	chr8:124421550-124421551	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs556135459	chr8:124421562-124421563	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs563270646	chr8:124421580-124421581	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs574694775	chr8:124421584-124421585	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs541629558	chr8:124421588-124421589	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs4006575	chr8:124421623-124421624	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
37	rs572187715	chr8:124421644-124421645	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs367953546	chr8:124421645-124421646	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs184733212	chr8:124421656-124421657	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs376394649	chr8:124421668-124421669	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs369720144	chr8:124421688-124421689	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs147808552	chr8:124421715-124421716	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs568058964	chr8:124421765-124421766	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs537685995	chr8:124421814-124421815	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs113377527	chr8:124421822-124421823	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs570997593	chr8:124421826-124421827	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs562319536	chr8:124421834-124421835	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs28407620	chr8:124421852-124421853	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs540154425	chr8:124421932-124421933	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs141233204	chr8:124421943-124421944	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:144)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Ewing''s sarcoma	21437220	CNVD
Autism	19415332	CNVD
Malaria	21533027	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Esophageal cancer	21851588	CNVD
Gastric cancer	17908304	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Liver carcinoma	19366792	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Testicular cancer	18059402	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
abnormal development	18461090	CNVD
Oral cancer	21386901	CNVD
Uveal melanoma	21693616	CNVD
Langer-Giedion syndrome	22283845	CNVD
Cancer	21637783	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	20632083	CNVD
Breast cancer	17603634	CNVD
Breast cancer	19602461	CNVD
Cancer	22429812	CNVD
Endometrial cancer	22040021	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oral cancer	19627613	CNVD
Prostate cancer	21088497	CNVD
colon cancer	17210682	CNVD
Breast cancer	21264507	CNVD
Breast cancer	22028636	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	16751803	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Gastric cancer	17167181	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	16461572	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
head and neck squamous cell carcinoma	18028549	CNVD
Breast cancer	17001317	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Prostate cancer	18632612	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Adenocarcinoma	21044232	CNVD
Squamous cell cancer	20885788	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	21399628	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	17393978	CNVD
Burkitt''s lymphoma	18698080	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Breast cancer	17899364	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Developmental delay	21147756	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Congenital diaphragmatic hernia	21525063	CNVD
Non-small cell lung cancer	19010865	CNVD
small cell lung cancer	20016488	CNVD
Papillary thyroid cancer	17515504	CNVD
Basal cell lymphoma	17053054	CNVD
Breast cancer	20932292	CNVD
Gastric cancer	22539939	CNVD
Breast cancer	22056952	CNVD
Langer-Giedion syndrome	16773131	CNVD
Lung cancer	16740712	CNVD
Mental retardation	16773131	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Langer-Giedion syndrome	22470819	CNVD
Cornelia de Lange syndrome	24599119	CNVD
Gastric cancer	21528007	CNVD
Breast cancer	22532251	CNVD
Cervical cancer	21062161	CNVD
Cancer	21129771	CNVD
benign familial neonatal convulsions	18472482	CNVD
Breast cancer	16417655	CNVD
Astrocytoma	17387387	CNVD
Cancer	21183584	CNVD
Follicular lymphoma	20505157	CNVD
T-cell lymphomas	19863542	CNVD
Colorectal cancer	20709793	CNVD
Medulloblastoma	20607354	CNVD
Breast cancer	20814816	CNVD
Colorectal cancer	22486879	CNVD
Breast cancer	17908964	CNVD
Colorectal cancer	20031965	CNVD
Hepatocellular carcinoma	16750200	CNVD
Ovarian cancer	17908964	CNVD
Ovarian cancer	20031965	CNVD
Prostate cancer	20031965	CNVD
Non-small cell lung cancer	17643093	CNVD
Prostate cancer	19242612	CNVD
Colorectal cancer	16774939	CNVD
Multiple myeloma	17550852	CNVD
Glioblastoma multiforme	18628472	CNVD
Malignant melanoma	17260012	CNVD
Intracranial aneurysm	16715129	CNVD
Breast cancer	16397240	CNVD
Multiple myeloma	16461302	CNVD
Multiple myeloma	16616336	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Breast cancer	21364760	CNVD
Burkitt''s lymphoma	20823134	CNVD
Colorectal cancer	21645411	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Acute myeloid leukemia	17268525	CNVD
Acute myeloid leukemia	18379011	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Oral squamous cell carcinoma	21853135	CNVD
Breast cancer	21611746	CNVD
Pancreatic cancer	17952125	CNVD
Ductal carcinoma	22052326	CNVD
Cancer	20164919	CNVD
T-cell lymphomas	22341440	CNVD
Breast cancer	22522925	CNVD
Prostate cancer	22341455	CNVD

Chromatin state (count:895 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:124409400-124421400	Weak transcription	Right Ventricle	heart
2	chr8:124409400-124424800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
3	chr8:124409400-124427600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
4	chr8:124409400-124427600	Weak transcription	A549	lung
5	chr8:124409400-124428000	Weak transcription	Brain Anterior Caudate	brain
6	chr8:124409600-124424600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
7	chr8:124409600-124424800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
8	chr8:124409800-124424600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr8:124409800-124427800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
10	chr8:124414400-124425000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
11	chr8:124416200-124424200	Weak transcription	Ovary	ovary
12	chr8:124416200-124424800	Weak transcription	Fetal Intestine Small	intestine
13	chr8:124416200-124425800	Weak transcription	Left Ventricle	heart
14	chr8:124416200-124427800	Weak transcription	Pancreas	Pancrea
15	chr8:124416800-124424200	Weak transcription	Fetal Heart	heart
16	chr8:124417800-124421800	Enhancers	HepG2	liver
17	chr8:124418400-124428200	Weak transcription	Skeletal Muscle Female	skeletal muscle
18	chr8:124420200-124424800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr8:124420400-124425000	Weak transcription	Monocytes-CD14+_RO01746	blood
20	chr8:124421200-124424200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
21	chr8:124421400-124421600	Strong transcription	Right Ventricle	heart
22	chr8:124421400-124428200	Weak transcription	Brain Inferior Temporal Lobe	brain
23	chr8:124421600-124421800	Genic enhancers	Right Ventricle	heart
24	chr8:124421800-124422000	Strong transcription	Right Ventricle	heart
25	chr8:124421800-124424200	Weak transcription	HepG2	liver
26	chr8:124422000-124427800	Weak transcription	Right Ventricle	heart
27	chr8:124422400-124428200	Weak transcription	Aorta	Aorta
28	chr8:124422600-124428000	Weak transcription	Stomach Smooth Muscle	stomach
29	chr8:124422800-124425000	Weak transcription	HSMM	muscle
30	chr8:124422800-124428200	Weak transcription	Brain Cingulate Gyrus	brain
31	chr8:124424200-124424400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
32	chr8:124424200-124425200	Enhancers	Ovary	ovary
33	chr8:124424200-124425400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr8:124424200-124425600	Enhancers	Pancreatic Islets	Pancreatic Islet
35	chr8:124424200-124425600	Enhancers	HepG2	liver
36	chr8:124424200-124425800	Enhancers	Fetal Heart	heart
37	chr8:124424400-124425400	Enhancers	Osteobl	bone
38	chr8:124424400-124428200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
39	chr8:124424600-124426200	Enhancers	Fetal Intestine Large	intestine
40	chr8:124424600-124426600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
41	chr8:124424600-124426600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
42	chr8:124424800-124425600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr8:124424800-124426000	Enhancers	Placenta	Placenta
44	chr8:124424800-124426000	Enhancers	NHLF	lung
45	chr8:124424800-124426200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
46	chr8:124424800-124426200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
47	chr8:124424800-124426200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
48	chr8:124424800-124426200	Enhancers	Fetal Intestine Small	intestine
49	chr8:124424800-124426200	Enhancers	Fetal Lung	lung
50	chr8:124424800-124426200	Enhancers	HSMMtube	muscle

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