Variant report

Variant	esv3435944
Chromosome Location	chr20:1206002-1207250
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:193)
CpG islands
(count:611)
Chromatin interactive
region (count:7)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:193 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF3	chr20:1206598-1206814	K562	blood:	n/a	chr20:1206710-1206718
2	BACH1	chr20:1206692-1207487	H1-hESC	embryonic stem cell:	n/a	n/a
3	BRCA1	chr20:1207083-1207091	HepG2	liver:	n/a	n/a
4	CBX3	chr20:1206593-1206825	K562	blood:	n/a	n/a
5	CCNT2	chr20:1206635-1207632	K562	blood:	n/a	n/a
6	CEBPB	chr20:1205923-1206215	HepG2	liver:	n/a	n/a
7	CEBPD	chr20:1206481-1207088	HepG2	liver:	n/a	n/a
8	CHD2	chr20:1206481-1206676	Hela-S3	cervix:	n/a	n/a
9	CHD2	chr20:1206710-1206791	K562	blood:	n/a	n/a
10	CHD2	chr20:1206778-1206779	H1-hESC	embryonic stem cell:	n/a	n/a
11	CREB1	chr20:1206599-1206982	A549	lung:	n/a	n/a
12	CTBP2	chr20:1206826-1207358	H1-hESC	embryonic stem cell:	n/a	n/a
13	CTCF	chr20:1206639-1206786	Fibrobl	skin:	n/a	n/a
14	CTCF	chr20:1206660-1206810	HUVEC	blood vessel:	n/a	n/a
15	CTCF	chr20:1206580-1206730	WERI-Rb-1	eye:	n/a	n/a
16	CTCF	chr20:1206676-1206742	Pancreas_OC	pancreas:	n/a	n/a
17	CTCF	chr20:1206706-1206777	A549	lung:	n/a	n/a
18	CTCF	chr20:1206640-1206790	SK-N-SH_RA	brain:	n/a	n/a
19	CTCF	chr20:1206170-1206251	H1-hESC	embryonic stem cell:	n/a	n/a
20	CTCF	chr20:1206600-1206750	AG04449	skin:	n/a	n/a
21	CTCF	chr20:1207137-1207187	Fibrobl	skin:	n/a	n/a
22	CTCF	chr20:1206600-1206750	HMEC	breast:	n/a	n/a
23	CTCF	chr20:1206633-1207896	SK-N-SH	brain:	n/a	n/a
24	CTCF	chr20:1206703-1206766	Lung_OC	lung:	n/a	n/a
25	CTCF	chr20:1206693-1206793	K562	blood:	n/a	n/a
26	CTCF	chr20:1206657-1206728	LNCaP	prostate:	n/a	n/a
27	E2F4	chr20:1206629-1206868	MCF10A-Er-Src	breast:	n/a	n/a
28	E2F6	chr20:1206579-1207319	H1-hESC	embryonic stem cell:	n/a	chr20:1206879-1206888 chr20:1206875-1206885 chr20:1206876-1206886
29	E2F6	chr20:1206545-1207671	A549	lung:	n/a	chr20:1206879-1206888 chr20:1206875-1206885 chr20:1207390-1207402 chr20:1206876-1206886
30	E2F6	chr20:1206775-1206976	K562	blood:	n/a	chr20:1206879-1206888 chr20:1206875-1206885 chr20:1206876-1206886
31	E2F6	chr20:1206570-1207243	A549	lung:	n/a	chr20:1206879-1206888 chr20:1206875-1206885 chr20:1206876-1206886
32	E2F6	chr20:1207208-1207382	K562	blood:	n/a	n/a
33	E2F6	chr20:1206584-1207067	K562	blood:	n/a	chr20:1206879-1206888 chr20:1206875-1206885 chr20:1206876-1206886
34	E2F6	chr20:1206580-1207383	H1-hESC	embryonic stem cell:	n/a	chr20:1206879-1206888 chr20:1206875-1206885 chr20:1206876-1206886
35	ELF1	chr20:1207009-1207283	K562	blood:	n/a	n/a
36	ELF1	chr20:1206741-1207310	GM12878	blood:	n/a	n/a
37	ELK1	chr20:1206806-1206917	K562	blood:	n/a	n/a
38	EP300	chr20:1206749-1206911	HepG2	liver:	n/a	chr20:1206844-1206853 chr20:1206877-1206886
39	EP300	chr20:1207056-1207194	K562	blood:	n/a	n/a
40	ETS1	chr20:1206612-1206809	K562	blood:	n/a	n/a
41	GABPA	chr20:1206044-1206264	H1-hESC	embryonic stem cell:	n/a	n/a
42	GTF2F1	chr20:1206679-1207053	K562	blood:	n/a	n/a
43	HA-E2F1	chr20:1206682-1207201	MCF-7	breast:	n/a	chr20:1206879-1206888 chr20:1206875-1206885 chr20:1206876-1206886
44	HCFC1	chr20:1206859-1206860	K562	blood:	n/a	n/a
45	HEY1	chr20:1206615-1206920	K562	blood:	n/a	n/a
46	HEY1	chr20:1206647-1206920	K562	blood:	n/a	n/a
47	HMGN3	chr20:1206678-1207310	K562	blood:	n/a	n/a
48	IRF1	chr20:1206674-1206917	K562	blood:	n/a	n/a
49	IRF1	chr20:1206405-1206887	K562	blood:	n/a	n/a
50	JUND	chr20:1206991-1206995	H1-hESC	embryonic stem cell:	n/a	n/a

(count:611 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr20:1206693-1206743	BJ	skin:	n/a
2	chr20:1206693-1206743	BJ	skin:	n/a
3	chr20:1206700-1206750	LNCaP	prostate:	n/a
4	chr20:1207118-1207168	HEK293	kidney:	embryo
5	chr20:1206700-1206750	RPTEC	kidney:	n/a
6	chr20:1206693-1206743	MCF10A-Er-Src	breast:	n/a
7	chr20:1206255-1206305	ProgFib	skin:	n/a
8	chr20:1206758-1206808	HPAEpiC	pulmonary alveolar:	n/a
9	chr20:1206739-1206789	SK-N-SH_RA	brain:	n/a
10	chr20:1207118-1207168	GM19239	blood:	n/a
11	chr20:1206830-1206880	T-47D	breast:	n/a
12	chr20:1206739-1206789	ProgFib	skin:	n/a
13	chr20:1206700-1206750	GM12892	blood:	n/a
14	chr20:1206255-1206305	HPAEpiC	pulmonary alveolar:	n/a
15	chr20:1206758-1206808	BE2_C	brain:	n/a
16	chr20:1206830-1206880	GM12892	blood:	n/a
17	chr20:1206806-1206856	HEK293	kidney:	embryo
18	chr20:1206703-1206753	GM19239	blood:	n/a
19	chr20:1206758-1206808	NHBE	bronchial:	n/a
20	chr20:1206682-1206732	BJ	skin:	n/a
21	chr20:1206693-1206743	HL-60	blood:	n/a
22	chr20:1206806-1206856	HMEC	breast:	n/a
23	chr20:1206255-1206305	GM12878	blood:	n/a
24	chr20:1206703-1206753	GM12878	blood:	n/a
25	chr20:1206806-1206856	RPTEC	kidney:	n/a
26	chr20:1206758-1206808	GM19239	blood:	n/a
27	chr20:1206682-1206732	GM12892	blood:	n/a
28	chr20:1206700-1206750	MCF10A-Er-Src	breast:	n/a
29	chr20:1206693-1206743	AG04450	lung:	fetal
30	chr20:1206739-1206789	NT2-D1	testis:	n/a
31	chr20:1206703-1206753	AG04450	lung:	fetal
32	chr20:1206758-1206808	AG04449	skin:	fetal
33	chr20:1206693-1206743	AG10803	skin:	n/a
34	chr20:1206739-1206789	HEEpiC	esophagus:	n/a
35	chr20:1206703-1206753	IMR90	lung:	fetal
36	chr20:1206830-1206880	HPAEpiC	pulmonary alveolar:	n/a
37	chr20:1206703-1206753	AG04449	skin:	fetal
38	chr20:1206703-1206753	H1-hESC	embryonic stem cell:	embryo
39	chr20:1206830-1206880	HCF	heart:	n/a
40	chr20:1206255-1206305	H1-hESC	embryonic stem cell:	embryo
41	chr20:1206255-1206305	HCT-116	colon:	n/a
42	chr20:1206255-1206305	K562	blood:	n/a
43	chr20:1206700-1206750	NH-A	brain:	n/a
44	chr20:1206682-1206732	PFSK-1	brain:	n/a
45	chr20:1206682-1206732	MCF10A-Er-Src	breast:	n/a
46	chr20:1206758-1206808	SK-N-SH_RA	brain:	n/a
47	chr20:1206255-1206305	AG04450	lung:	fetal
48	chr20:1207118-1207168	Hepatocyte	liver:	n/a
49	chr20:1206758-1206808	HMEC	breast:	n/a
50	chr20:1206739-1206789	HAEpiC	amniotic membrane:	n/a

(count:7 , 50 per page) page: 1

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

No data

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

Extended variants
information (count: 38 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:38 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	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
2	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
3	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
4	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
5	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
6	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
7	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
8	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
9	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
10	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
11	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
12	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
13	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
14	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
15	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
16	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
17	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
18	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
19	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
20	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
21	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
22	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
23	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
24	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
25	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
26	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
27	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
28	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
29	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
30	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
31	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
32	rs202040875	chr20:1207056-1207057	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
33	rs140209361	chr20:1207088-1207089	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
34	rs442262	chr20:1207138-1207139	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
35	rs13038444	chr20:1207189-1207190	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
36	rs181708836	chr20:1207197-1207198	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
37	rs545894936	chr20:1207206-1207207	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
38	rs186906589	chr20:1207221-1207222	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription 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:278 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:1205800-1206800	Bivalent/Poised TSS	Cortex derived primary cultured neurospheres	brain
2	chr20:1205800-1207000	Active TSS	Breast Myoepithelial Primary Cells	Breast
3	chr20:1205800-1207000	Active TSS	A549	lung
4	chr20:1205800-1207200	Active TSS	HUES48 Cell Line	embryonic stem cell
5	chr20:1205800-1207400	Active TSS	Primary T cells from cord blood	blood
6	chr20:1205800-1207600	Active TSS	ES-I3 Cell Line	embryonic stem cell
7	chr20:1205800-1207600	Active TSS	Pancreatic Islets	Pancreatic Islet
8	chr20:1205800-1207800	Active TSS	H9 Cell Line	embryonic stem cell
9	chr20:1205800-1207800	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
10	chr20:1205800-1207800	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
11	chr20:1205800-1207800	Active TSS	Brain Cingulate Gyrus	brain
12	chr20:1206000-1206200	Flanking Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
13	chr20:1206000-1206200	Flanking Bivalent TSS/Enh	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr20:1206000-1206200	Flanking Bivalent TSS/Enh	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr20:1206000-1206200	Flanking Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
16	chr20:1206000-1206200	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
17	chr20:1206000-1206200	Flanking Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
18	chr20:1206000-1206200	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood
19	chr20:1206000-1206200	Flanking Bivalent TSS/Enh	Primary T cells fromperipheralblood	blood
20	chr20:1206000-1206200	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
21	chr20:1206000-1206200	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
22	chr20:1206000-1206200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
23	chr20:1206000-1206200	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
24	chr20:1206000-1206200	Flanking Bivalent TSS/Enh	Primary T helper 17 cells PMA-I stimulated	--
25	chr20:1206000-1206200	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
26	chr20:1206000-1206200	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
27	chr20:1206000-1206200	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Female	--
28	chr20:1206000-1206200	Flanking Active TSS	Muscle Satellite Cultured Cells	--
29	chr20:1206000-1206200	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
30	chr20:1206000-1206200	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
31	chr20:1206000-1206200	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
32	chr20:1206000-1206200	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
33	chr20:1206000-1206200	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
34	chr20:1206000-1206200	Flanking Active TSS	Adipose Nuclei	Adipose
35	chr20:1206000-1206200	Flanking Bivalent TSS/Enh	Brain Germinal Matrix	brain
36	chr20:1206000-1206200	Flanking Bivalent TSS/Enh	Brain Dorsolateral Prefrontal Cortex	brain
37	chr20:1206000-1206200	Flanking Active TSS	Colonic Mucosa	Colon
38	chr20:1206000-1206200	Flanking Bivalent TSS/Enh	Colon Smooth Muscle	Colon
39	chr20:1206000-1206200	Flanking Bivalent TSS/Enh	Fetal Adrenal Gland	Adrenal Gland
40	chr20:1206000-1206200	Flanking Active TSS	Fetal Intestine Small	intestine
41	chr20:1206000-1206200	Flanking Bivalent TSS/Enh	Fetal Muscle Trunk	muscle
42	chr20:1206000-1206200	Flanking Bivalent TSS/Enh	Fetal Muscle Leg	muscle
43	chr20:1206000-1206200	Flanking Bivalent TSS/Enh	Placenta	Placenta
44	chr20:1206000-1206200	Enhancers	Gastric	stomach
45	chr20:1206000-1206200	Flanking Active TSS	Ovary	ovary
46	chr20:1206000-1206200	Flanking Bivalent TSS/Enh	Rectal Mucosa Donor 29	rectum
47	chr20:1206000-1206200	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
48	chr20:1206000-1206200	Flanking Bivalent TSS/Enh	Skeletal Muscle Male	skeletal muscle
49	chr20:1206000-1206200	Flanking Bivalent TSS/Enh	Stomach Smooth Muscle	stomach
50	chr20:1206000-1206200	Flanking Bivalent TSS/Enh	HepG2	liver

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