Variant report

Variant	esv3509885
Chromosome Location	chr20:1205427-1207700
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:325)
CpG islands
(count:732)
Chromatin interactive
region (count:8)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:325 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr20:1207455-1207579	K562	blood:	n/a	n/a
2	ATF3	chr20:1206598-1206814	K562	blood:	n/a	chr20:1206710-1206718
3	BACH1	chr20:1206692-1207487	H1-hESC	embryonic stem cell:	n/a	n/a
4	BHLHE40	chr20:1207265-1207297	K562	blood:	n/a	n/a
5	BRCA1	chr20:1207083-1207091	HepG2	liver:	n/a	n/a
6	CBX3	chr20:1207411-1207758	K562	blood:	n/a	n/a
7	CBX3	chr20:1206593-1206825	K562	blood:	n/a	n/a
8	CCNT2	chr20:1206635-1207632	K562	blood:	n/a	n/a
9	CEBPB	chr20:1207432-1207560	K562	blood:	n/a	n/a
10	CEBPB	chr20:1205923-1206215	HepG2	liver:	n/a	n/a
11	CEBPD	chr20:1206481-1207088	HepG2	liver:	n/a	n/a
12	CHD2	chr20:1206481-1206676	Hela-S3	cervix:	n/a	n/a
13	CHD2	chr20:1206710-1206791	K562	blood:	n/a	n/a
14	CHD2	chr20:1206778-1206779	H1-hESC	embryonic stem cell:	n/a	n/a
15	CREB1	chr20:1206599-1206982	A549	lung:	n/a	n/a
16	CTBP2	chr20:1206826-1207358	H1-hESC	embryonic stem cell:	n/a	n/a
17	CTCF	chr20:1207500-1207650	NHLF	lung:	n/a	n/a
18	CTCF	chr20:1207500-1207650	NHDF-neo	bronchial:	n/a	n/a
19	CTCF	chr20:1207500-1207650	HCFaa	heart:	n/a	n/a
20	CTCF	chr20:1207507-1207644	Lung_OC	lung:	n/a	n/a
21	CTCF	chr20:1207500-1207650	HA-sp	spinal cord:	n/a	n/a
22	CTCF	chr20:1207480-1207630	K562	blood:	n/a	n/a
23	CTCF	chr20:1207480-1207630	AG10803	skin:	n/a	n/a
24	CTCF	chr20:1207440-1207590	HFF-Myc	foreskin:	n/a	n/a
25	CTCF	chr20:1207460-1207684	K562	blood:	n/a	n/a
26	CTCF	chr20:1207137-1207187	Fibrobl	skin:	n/a	n/a
27	CTCF	chr20:1207500-1207650	RPTEC	kidney:	n/a	n/a
28	CTCF	chr20:1207500-1207650	GM12867	blood:	n/a	n/a
29	CTCF	chr20:1207500-1207650	HBMEC	blood vessel:	n/a	n/a
30	CTCF	chr20:1207499-1207614	HUVEC	blood vessel:	n/a	n/a
31	CTCF	chr20:1206600-1206750	HMEC	breast:	n/a	n/a
32	CTCF	chr20:1207550-1207711	GM12891	blood:	n/a	n/a
33	CTCF	chr20:1207480-1207630	AG09309	skin:	n/a	n/a
34	CTCF	chr20:1207500-1207650	Caco-2	colon:	n/a	n/a
35	CTCF	chr20:1207500-1207650	HCPEpiC	choroid plexus:	n/a	n/a
36	CTCF	chr20:1206703-1206766	Lung_OC	lung:	n/a	n/a
37	CTCF	chr20:1207480-1207630	HEEpiC	esophagus:	n/a	n/a
38	CTCF	chr20:1207520-1207670	A549	lung:	n/a	n/a
39	CTCF	chr20:1207504-1207666	MCF-7	breast:	n/a	n/a
40	CTCF	chr20:1207473-1207688	SK-N-SH_RA	brain:	n/a	n/a
41	CTCF	chr20:1207484-1207690	HepG2	liver:	n/a	n/a
42	CTCF	chr20:1207526-1207701	H1-hESC	embryonic stem cell:	n/a	n/a
43	CTCF	chr20:1207560-1207710	HPF	lung:	n/a	n/a
44	CTCF	chr20:1207460-1207610	HEEpiC	esophagus:	n/a	n/a
45	CTCF	chr20:1207460-1207610	AG10803	skin:	n/a	n/a
46	CTCF	chr20:1207460-1207610	HMEC	breast:	n/a	n/a
47	CTCF	chr20:1207510-1207706	GM19240	blood:	n/a	n/a
48	CTCF	chr20:1207568-1207691	GM20000	blood:	n/a	n/a
49	CTCF	chr20:1207500-1207650	HPF	lung:	n/a	n/a
50	CTCF	chr20:1207520-1207670	HCT-116	colon:	n/a	n/a

(count:732 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr20:1207118-1207168	HNPCEpiC	eye:	n/a
2	chr20:1206700-1206750	NHDF-neo	bronchial:	n/a
3	chr20:1206255-1206305	Caco-2	colon:	n/a
4	chr20:1206693-1206743	HCT-116	colon:	n/a
5	chr20:1206739-1206789	HAEpiC	amniotic membrane:	n/a
6	chr20:1206693-1206743	AG04450	lung:	fetal
7	chr20:1205378-1205428	NHDF-neo	bronchial:	n/a
8	chr20:1206758-1206808	SAEC	small airway:	n/a
9	chr20:1206830-1206880	K562	blood:	n/a
10	chr20:1206806-1206856	AG09319	gingival:	n/a
11	chr20:1206682-1206732	BE2_C	brain:	n/a
12	chr20:1206693-1206743	NHDF-neo	bronchial:	n/a
13	chr20:1206806-1206856	AG10803	skin:	n/a
14	chr20:1205378-1205428	NH-A	brain:	n/a
15	chr20:1205378-1205428	U87	brain:	n/a
16	chr20:1206700-1206750	HRPEpiC	eye:	n/a
17	chr20:1205378-1205428	Jurkat	blood:	n/a
18	chr20:1206806-1206856	HCF	heart:	n/a
19	chr20:1206806-1206856	Hela-S3	cervix:	n/a
20	chr20:1206806-1206856	Jurkat	blood:	n/a
21	chr20:1206700-1206750	HRCEpiC	kidney:	n/a
22	chr20:1206830-1206880	Hela-S3	cervix:	n/a
23	chr20:1206700-1206750	U87	brain:	n/a
24	chr20:1206693-1206743	HL-60	blood:	n/a
25	chr20:1206830-1206880	HIPEpiC	eye:	n/a
26	chr20:1207383-1207433	SK-N-SH	brain:	n/a
27	chr20:1206693-1206743	CMK	blood:	n/a
28	chr20:1205378-1205428	HRCEpiC	kidney:	n/a
29	chr20:1206693-1206743	HRPEpiC	eye:	n/a
30	chr20:1206700-1206750	HCF	heart:	n/a
31	chr20:1206682-1206732	AG09319	gingival:	n/a
32	chr20:1206700-1206750	HAEpiC	amniotic membrane:	n/a
33	chr20:1206703-1206753	RPTEC	kidney:	n/a
34	chr20:1206255-1206305	MCF10A-Er-Src	breast:	n/a
35	chr20:1207118-1207168	GM12892	blood:	n/a
36	chr20:1206830-1206880	HRPEpiC	eye:	n/a
37	chr20:1206693-1206743	PFSK-1	brain:	n/a
38	chr20:1206700-1206750	AG09309	skin:	n/a
39	chr20:1207118-1207168	HMEC	breast:	n/a
40	chr20:1206830-1206880	HL-60	blood:	n/a
41	chr20:1206700-1206750	HEK293	kidney:	embryo
42	chr20:1206758-1206808	K562	blood:	n/a
43	chr20:1206693-1206743	HUVEC	blood vessel:	n/a
44	chr20:1206758-1206808	ProgFib	skin:	n/a
45	chr20:1206830-1206880	T-47D	breast:	n/a
46	chr20:1206703-1206753	Jurkat	blood:	n/a
47	chr20:1206806-1206856	GM12891	blood:	n/a
48	chr20:1205378-1205428	GM06990	blood:	n/a
49	chr20:1206703-1206753	AoSMC	blood vessel:	n/a
50	chr20:1207118-1207168	HL-60	blood:	n/a

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr20:1206916..1209904-chr20:1219433..1221518,2	K562	blood:
2	chr20:1206512..1208051-chr20:1245857..1247433,2	K562	blood:
3	chr20:1207352..1209653-chr20:1227300..1229207,2	K562	blood:
4	chr20:1206796..1208958-chr20:1209065..1211253,2	MCF-7	breast:
5	chr20:1206971..1208847-chr20:1236164..1237785,2	K562	blood:
6	chr20:1204614..1208313-chr20:1245857..1250887,4	K562	blood:
7	chr20:1206586..1208814-chr20:1304748..1306483,2	K562	blood:
8	chr20:1207162..1208733-chr20:1230513..1232075,2	K562	blood:

No data

Variant related genes	Relation type
RAD21L1	TF binding region
RAD21L1	CpG island
ENSG00000125775	chromatin interactions
ENSG00000244588	chromatin interactions
ENSG00000101298	chromatin interactions
ENSG00000234684	chromatin interactions

Extended variants
information (count: 77 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:77 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs552160538	chr20:1205430-1205431	Enhancers Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs75350233	chr20:1205497-1205498	Enhancers Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs531222837	chr20:1205506-1205507	Enhancers Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs550928375	chr20:1205524-1205525	Enhancers Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs577060498	chr20:1205574-1205575	Enhancers Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs567826361	chr20:1205580-1205581	Enhancers Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs368893444	chr20:1205584-1205585	Enhancers Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs544389713	chr20:1205610-1205611	Bivalent Enhancer Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs561292362	chr20:1205612-1205613	Bivalent Enhancer Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs536420111	chr20:1205632-1205633	Bivalent Enhancer Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs547089073	chr20:1205653-1205654	Bivalent Enhancer Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs372041494	chr20:1205716-1205717	Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs76115200	chr20:1205762-1205763	Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs552109108	chr20:1205816-1205817	Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs565542568	chr20:1205817-1205818	Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs397020	chr20:1205886-1205887	Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance disease
17	rs58696255	chr20:1205892-1205893	Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs78405220	chr20:1205895-1205896	Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs540018787	chr20:1205946-1205947	Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs189865363	chr20:1206011-1206012	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs546140363	chr20:1206016-1206017	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs74456755	chr20:1206062-1206063	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs545856350	chr20:1206095-1206096	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs6109022	chr20:1206098-1206099	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs6109023	chr20:1206107-1206108	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs531260099	chr20:1206115-1206116	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs6078231	chr20:1206145-1206146	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs6040753	chr20:1206194-1206195	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs396004	chr20:1206238-1206239	Active TSS Bivalent/Poised TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs446359	chr20:1206272-1206273	Active TSS Bivalent/Poised TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs541450167	chr20:1206283-1206284	Active TSS Bivalent/Poised TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs71919256	chr20:1206284-1206285	Active TSS Bivalent/Poised TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs546834609	chr20:1206302-1206303	Active TSS Bivalent/Poised TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs59841173	chr20:1206303-1206304	Active TSS Bivalent/Poised TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs552398746	chr20:1206427-1206428	Active TSS Bivalent/Poised TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs111434597	chr20:1206431-1206432	Active TSS Bivalent/Poised TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs549944837	chr20:1206528-1206529	Active TSS Bivalent/Poised TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs552150887	chr20:1206534-1206535	Active TSS Bivalent/Poised TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs113476701	chr20:1206615-1206616	Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs113664174	chr20:1206632-1206633	Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs566668756	chr20:1206700-1206701	Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs112121489	chr20:1206717-1206718	Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs538735630	chr20:1206722-1206723	Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs552184119	chr20:1206733-1206734	Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs568886680	chr20:1206751-1206752	Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs537822368	chr20:1206759-1206760	Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs571243105	chr20:1206842-1206843	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Enhancers	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
48	rs377175935	chr20:1206857-1206858	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Enhancers	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
49	rs117557888	chr20:1206860-1206861	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Enhancers	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
50	rs574602726	chr20:1206946-1206947	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:64)

Disease	PMID	Source
Hodgkin''s lymphoma	18641027	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
Glioblastoma multiforme	22286061	CNVD
Hepatocellular carcinoma	22174799	CNVD
Colorectal cancer	19455253	CNVD
Ovarian cancer	20844748	CNVD
Breast cancer	17603634	CNVD
Colorectal cancer	19359472	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Intracranial aneurysm	16715129	CNVD
Colorectal cancer	16774939	CNVD
Autism	18414403	CNVD
Neurocytoma	17123091	CNVD
Medulloblastoma	21979893	CNVD
Breast cancer	16397240	CNVD
abortions and stillbirths	19751515	CNVD
Wilms tumour	21544195	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	16272173	CNVD
Melanoma	18172304	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Oral cancer	19627613	CNVD
colon cancer	17210682	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	21080181	CNVD
Thyroid cancer	19087340	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Human rectal carcinomas	16397240	CNVD
Olfactory neuroblastoma	18408657	CNVD
Central neurocytomas	17123091	CNVD
Colorectal cancer	16272173	CNVD
Gastric cancer	17908304	CNVD
Urothelial carcinoma	21177765	CNVD
lymphocytic leukemia	21291569	CNVD
Acute myeloid leukemia	20729466	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Ewing''s sarcoma	17952124	CNVD
Oral cancer	21386901	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Lung cancer	18438408	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Colorectal cancer	21645411	CNVD
small cell lung cancer	20016488	CNVD
Melanoma	17363583	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:360 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:1204200-1206000	Weak transcription	Psoas Muscle	Psoas
2	chr20:1205000-1205800	Enhancers	K562	blood
3	chr20:1205400-1205600	Enhancers	Primary T regulatory cells fromperipheralblood	blood
4	chr20:1205400-1205800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
5	chr20:1205400-1205800	Bivalent Enhancer	HepG2	liver
6	chr20:1205600-1205800	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
7	chr20:1205600-1205800	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
8	chr20:1205600-1206000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
9	chr20:1205600-1206000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
10	chr20:1205600-1206000	Enhancers	Fetal Intestine Large	intestine
11	chr20:1205800-1206000	Flanking Bivalent TSS/Enh	HUES6 Cell Line	embryonic stem cell
12	chr20:1205800-1206000	Flanking Bivalent TSS/Enh	HUES64 Cell Line	embryonic stem cell
13	chr20:1205800-1206000	Flanking Bivalent TSS/Enh	iPS-15b Cell Line	embryonic stem cell
14	chr20:1205800-1206000	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
15	chr20:1205800-1206000	Active TSS	Primary T helper naive cells fromperipheralblood	blood
16	chr20:1205800-1206000	Enhancers	Primary T helper cells fromperipheralblood	blood
17	chr20:1205800-1206000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
18	chr20:1205800-1206000	Enhancers	Brain Inferior Temporal Lobe	brain
19	chr20:1205800-1206000	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
20	chr20:1205800-1206000	Enhancers	Pancreas	Pancrea
21	chr20:1205800-1206000	Bivalent/Poised TSS	HepG2	liver
22	chr20:1205800-1206000	Flanking Active TSS	K562	blood
23	chr20:1205800-1206000	Active TSS	NHEK	skin
24	chr20:1205800-1206800	Bivalent/Poised TSS	Cortex derived primary cultured neurospheres	brain
25	chr20:1205800-1207000	Active TSS	Breast Myoepithelial Primary Cells	Breast
26	chr20:1205800-1207000	Active TSS	A549	lung
27	chr20:1205800-1207200	Active TSS	HUES48 Cell Line	embryonic stem cell
28	chr20:1205800-1207400	Active TSS	Primary T cells from cord blood	blood
29	chr20:1205800-1207600	Active TSS	ES-I3 Cell Line	embryonic stem cell
30	chr20:1205800-1207600	Active TSS	Pancreatic Islets	Pancreatic Islet
31	chr20:1205800-1207800	Active TSS	H9 Cell Line	embryonic stem cell
32	chr20:1205800-1207800	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
33	chr20:1205800-1207800	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
34	chr20:1205800-1207800	Active TSS	Brain Cingulate Gyrus	brain
35	chr20:1206000-1206200	Flanking Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
36	chr20:1206000-1206200	Flanking Bivalent TSS/Enh	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr20:1206000-1206200	Flanking Bivalent TSS/Enh	H9 Derived Neuron Cultured Cells	ES cell derived
38	chr20:1206000-1206200	Flanking Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
39	chr20:1206000-1206200	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
40	chr20:1206000-1206200	Flanking Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
41	chr20:1206000-1206200	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood
42	chr20:1206000-1206200	Flanking Bivalent TSS/Enh	Primary T cells fromperipheralblood	blood
43	chr20:1206000-1206200	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
44	chr20:1206000-1206200	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
45	chr20:1206000-1206200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
46	chr20:1206000-1206200	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
47	chr20:1206000-1206200	Flanking Bivalent TSS/Enh	Primary T helper 17 cells PMA-I stimulated	--
48	chr20:1206000-1206200	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
49	chr20:1206000-1206200	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
50	chr20:1206000-1206200	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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