Variant report

Variant	esv3379456
Chromosome Location	chr11:71496804-71499952
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:576)
CpG islands
(count:489)
Chromatin interactive
region (count:6)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:576 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:71499570-71499575	HepG2	liver:	n/a	n/a
2	BATF	chr11:71499406-71499609	GM12878	blood:	n/a	n/a
3	BATF	chr11:71498902-71499183	GM12878	blood:	n/a	n/a
4	BATF	chr11:71499485-71499773	GM12878	blood:	n/a	n/a
5	BCL11A	chr11:71498971-71499169	GM12878	blood:	n/a	n/a
6	BCL11A	chr11:71498840-71499221	GM12878	blood:	n/a	chr11:71498863-71498876
7	BCL11A	chr11:71497628-71497822	GM12878	blood:	n/a	n/a
8	BHLHE40	chr11:71498569-71498859	GM12878	blood:	n/a	n/a
9	BHLHE40	chr11:71497790-71498250	GM12878	blood:	n/a	n/a
10	BHLHE40	chr11:71498674-71498871	K562	blood:	n/a	n/a
11	BHLHE40	chr11:71497885-71498210	K562	blood:	n/a	n/a
12	BHLHE40	chr11:71498981-71499167	HepG2	liver:	n/a	n/a
13	BHLHE40	chr11:71497560-71498099	HepG2	liver:	n/a	n/a
14	BRCA1	chr11:71498122-71498649	Hela-S3	cervix:	n/a	n/a
15	BRCA1	chr11:71499265-71499372	Hela-S3	cervix:	n/a	n/a
16	CBX3	chr11:71498809-71499238	K562	blood:	n/a	n/a
17	CCNT2	chr11:71497922-71498103	K562	blood:	n/a	n/a
18	CEBPB	chr11:71499198-71499572	K562	blood:	n/a	chr11:71499369-71499380
19	CEBPB	chr11:71499184-71499569	IMR90	lung:	n/a	chr11:71499369-71499380
20	CEBPB	chr11:71499194-71499546	A549	lung:	n/a	chr11:71499369-71499380
21	CEBPB	chr11:71498481-71498685	Hela-S3	cervix:	n/a	n/a
22	CEBPB	chr11:71499270-71499540	A549	lung:	n/a	chr11:71499369-71499380
23	CEBPB	chr11:71499283-71499431	K562	blood:	n/a	chr11:71499369-71499380
24	CEBPB	chr11:71499184-71499559	K562	blood:	n/a	chr11:71499369-71499380
25	CEBPB	chr11:71499179-71499557	Hela-S3	cervix:	n/a	chr11:71499369-71499380
26	CEBPB	chr11:71499197-71499550	HepG2	liver:	n/a	chr11:71499369-71499380
27	CEBPD	chr11:71497637-71497944	HepG2	liver:	n/a	n/a
28	CEBPD	chr11:71498484-71498760	HepG2	liver:	n/a	n/a
29	CEBPD	chr11:71499281-71499614	K562	blood:	n/a	n/a
30	CHD2	chr11:71498288-71498302	H1-hESC	embryonic stem cell:	n/a	n/a
31	CHD2	chr11:71499189-71499317	Hela-S3	cervix:	n/a	n/a
32	CHD2	chr11:71498612-71498760	H1-hESC	embryonic stem cell:	n/a	n/a
33	CHD2	chr11:71498180-71498344	GM12878	blood:	n/a	n/a
34	CHD2	chr11:71498572-71498617	GM12878	blood:	n/a	n/a
35	CHD2	chr11:71497936-71497986	H1-hESC	embryonic stem cell:	n/a	n/a
36	CHD2	chr11:71497655-71498800	Hela-S3	cervix:	n/a	n/a
37	CREB1	chr11:71497807-71498855	A549	lung:	n/a	n/a
38	CREB1	chr11:71498004-71498774	HepG2	liver:	n/a	n/a
39	CTCF	chr11:71499140-71499290	AG04449	skin:	n/a	n/a
40	CTCF	chr11:71499000-71499150	HBMEC	blood vessel:	n/a	n/a
41	CTCF	chr11:71499207-71499229	HepG2	liver:	n/a	n/a
42	CTCF	chr11:71497955-71498038	Kidney_OC	kidney:	n/a	n/a
43	CTCF	chr11:71498540-71498690	GM12869	blood:	n/a	n/a
44	CTCF	chr11:71499215-71499237	H1-hESC	embryonic stem cell:	n/a	n/a
45	CTCF	chr11:71499240-71499390	BJ	skin:	n/a	n/a
46	CTCF	chr11:71499500-71499650	Caco-2	colon:	n/a	n/a
47	CTCF	chr11:71498500-71498650	SK-N-SH_RA	brain:	n/a	n/a
48	CTCF	chr11:71497887-71498036	Spleen_OC	spleen:	n/a	n/a
49	CTCF	chr11:71498720-71498870	AG04449	skin:	n/a	n/a
50	CTCF	chr11:71499202-71499281	NHEK	skin:	n/a	n/a

(count:489 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:71498609-71498659	HEEpiC	esophagus:	n/a
2	chr11:71498609-71498659	HEEpiC	esophagus:	n/a
3	chr11:71497575-71497625	IMR90	lung:	fetal
4	chr11:71497688-71497738	IMR90	lung:	fetal
5	chr11:71498609-71498659	AG10803	skin:	n/a
6	chr11:71498715-71498765	HEEpiC	esophagus:	n/a
7	chr11:71497688-71497738	AG10803	skin:	n/a
8	chr11:71498609-71498659	HCM	heart:	n/a
9	chr11:71499117-71499167	HRPEpiC	eye:	n/a
10	chr11:71497552-71497602	MCF10A-Er-Src	breast:	n/a
11	chr11:71498202-71498252	LNCaP	prostate:	n/a
12	chr11:71498715-71498765	Hela-S3	cervix:	n/a
13	chr11:71498715-71498765	HRPEpiC	eye:	n/a
14	chr11:71497575-71497625	HMEC	breast:	n/a
15	chr11:71497575-71497625	ECC-1	luminal epithelium:	n/a
16	chr11:71498715-71498765	HL-60	blood:	n/a
17	chr11:71499117-71499167	Caco-2	colon:	n/a
18	chr11:71497688-71497738	GM12878	blood:	n/a
19	chr11:71498715-71498765	HCPEpiC	choroid plexus:	n/a
20	chr11:71497575-71497625	AG09309	skin:	n/a
21	chr11:71498202-71498252	AoSMC	blood vessel:	n/a
22	chr11:71499006-71499056	MCF-7	breast:	n/a
23	chr11:71498609-71498659	HIPEpiC	eye:	n/a
24	chr11:71497552-71497602	HRCEpiC	kidney:	n/a
25	chr11:71499006-71499056	HepG2	liver:	n/a
26	chr11:71497575-71497625	SK-N-SH_RA	brain:	n/a
27	chr11:71498609-71498659	GM19239	blood:	n/a
28	chr11:71497552-71497602	A549	lung:	n/a
29	chr11:71498715-71498765	BE2_C	brain:	n/a
30	chr11:71499006-71499056	GM12878	blood:	n/a
31	chr11:71498715-71498765	HCM	heart:	n/a
32	chr11:71498202-71498252	HCPEpiC	choroid plexus:	n/a
33	chr11:71498202-71498252	T-47D	breast:	n/a
34	chr11:71498715-71498765	AG09309	skin:	n/a
35	chr11:71497552-71497602	NHBE	bronchial:	n/a
36	chr11:71497552-71497602	HCM	heart:	n/a
37	chr11:71498202-71498252	PANC-1	pancreas:	n/a
38	chr11:71498715-71498765	HNPCEpiC	eye:	n/a
39	chr11:71497552-71497602	Jurkat	blood:	n/a
40	chr11:71497575-71497625	U87	brain:	n/a
41	chr11:71498202-71498252	NH-A	brain:	n/a
42	chr11:71499006-71499056	Hela-S3	cervix:	n/a
43	chr11:71497552-71497602	HCPEpiC	choroid plexus:	n/a
44	chr11:71499006-71499056	Caco-2	colon:	n/a
45	chr11:71497575-71497625	SAEC	small airway:	n/a
46	chr11:71499006-71499056	PANC-1	pancreas:	n/a
47	chr11:71499006-71499056	SK-N-SH	brain:	n/a
48	chr11:71498715-71498765	GM12878	blood:	n/a
49	chr11:71497552-71497602	K562	blood:	n/a
50	chr11:71497688-71497738	HPAEpiC	pulmonary alveolar:	n/a

(count:6 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:67572484..67573077-chr11:71498421..71498985,2	HCT-116	colon:
2	chr11:71498143..71498944-chr16:5147397..5148064,2	Hela-S3	cervix:
3	chr11:3442224..3443750-chr11:71497854..71499382,2	MCF-7	breast:
4	chr11:71498340..71499087-chr19:18391666..18392636,2	Hela-S3	cervix:
5	chr11:71499803..71501328-chr11:71502237..71504426,2	K562	blood:
6	chr11:71498107..71498639-chr3:75483883..75484386,2	Hela-S3	cervix:

No data

Variant related genes	Relation type
FAM86C1	TF binding region
FAM86C1	CpG island
ENSG00000118894	chromatin interactions
ENSG00000130522	chromatin interactions
ENSG00000160172	chromatin interactions
ENSG00000166492	chromatin interactions
ENSG00000244026	chromatin interactions

Extended variants
information (count: 176 )
Associated
traits (count: 103 )

Variant overlapped rSNPs/rCNVs (count:176 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs574238718	chr11:71496808-71496809	Active TSS Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs9326464	chr11:71496812-71496813	Active TSS Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
3	rs9326465	chr11:71496878-71496879	Active TSS Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
4	rs9326466	chr11:71496890-71496891	Active TSS Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
5	rs182989807	chr11:71496894-71496895	Active TSS Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs565590990	chr11:71496909-71496910	Active TSS Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs112702728	chr11:71496986-71496987	Active TSS Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs532537665	chr11:71497005-71497006	Active TSS Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs551025668	chr11:71497022-71497023	Active TSS Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs562969577	chr11:71497029-71497030	Active TSS Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs187956220	chr11:71497076-71497077	Active TSS Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs535517092	chr11:71497092-71497093	Active TSS Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs113194975	chr11:71497108-71497109	Active TSS Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs548404483	chr11:71497125-71497126	Active TSS Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs190924333	chr11:71497142-71497143	Active TSS Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs149657791	chr11:71497210-71497211	Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs552037261	chr11:71497231-71497232	Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs371802954	chr11:71497267-71497268	Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs540171731	chr11:71497277-71497278	Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs570441453	chr11:71497292-71497293	Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs182316294	chr11:71497318-71497319	Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs144455068	chr11:71497340-71497341	Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs7127417	chr11:71497343-71497344	Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
24	rs187723832	chr11:71497344-71497345	Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs535484588	chr11:71497372-71497373	Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs553604561	chr11:71497383-71497384	Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs369932114	chr11:71497407-71497408	Active TSS Flanking Active TSS Bivalent/Poised TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs7111030	chr11:71497414-71497415	Active TSS Flanking Active TSS Bivalent/Poised TSS Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
29	rs11828600	chr11:71497437-71497438	Active TSS Flanking Active TSS Bivalent/Poised TSS Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs372189749	chr11:71497438-71497439	Active TSS Flanking Active TSS Bivalent/Poised TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs559274356	chr11:71497471-71497472	Active TSS Flanking Active TSS Bivalent/Poised TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs11828615	chr11:71497509-71497510	Active TSS Flanking Active TSS Bivalent/Poised TSS Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs544610055	chr11:71497520-71497521	Active TSS Flanking Active TSS Bivalent/Poised TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs562831674	chr11:71497528-71497529	Active TSS Flanking Active TSS Bivalent/Poised TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs530045464	chr11:71497531-71497532	Active TSS Flanking Active TSS Bivalent/Poised TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs34580079	chr11:71497558-71497559	Active TSS Flanking Active TSS Bivalent/Poised TSS Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
37	rs34092377	chr11:71497586-71497587	Active TSS Flanking Active TSS Bivalent/Poised TSS Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
38	rs542281731	chr11:71497606-71497607	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
39	rs560399240	chr11:71497615-71497616	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
40	rs113576471	chr11:71497616-71497617	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
41	rs573052533	chr11:71497626-71497627	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs7112161	chr11:71497631-71497632	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
43	rs7112165	chr11:71497649-71497650	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
44	rs549665390	chr11:71497657-71497658	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs568019644	chr11:71497675-71497676	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs11823841	chr11:71497678-71497679	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs553813064	chr11:71497689-71497690	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
48	rs7127938	chr11:71497693-71497694	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Enhancers	TF binding region CpG island	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
49	rs35226522	chr11:71497700-71497701	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
50	rs534392493	chr11:71497702-71497703	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:103)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Wilms tumour	21544195	CNVD
Autism	22495311	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Glioblastoma multiforme	21138945	CNVD
Acute myeloid leukemia	20729466	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	21637783	CNVD
Acute myeloid leukemia	16864856	CNVD
Chronic lymphocytic leukemia	21795749	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21484798	CNVD
Ewing''s sarcoma	21437220	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	20837533	CNVD
Breast cancer	21264507	CNVD
Cervical cancer	21063398	CNVD
Glioblastoma multiforme	19960244	CNVD
Liposarcoma	21253554	CNVD
Neuroblastoma	18923524	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Neuroblastoma	17533364	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Prostate cancer	18632612	CNVD
Smith-Lemli-Opitz syndrome	21572526	CNVD
Glioblastoma multiforme	21080181	CNVD
Multiple myeloma	16461302	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Chordoma	21602918	CNVD
Metanephric adenoma	20802469	CNVD
Melanoma	18172304	CNVD
Breast cancer	21806811	CNVD
Breast cancer	22002566	CNVD
Ductal carcinoma	18381933	CNVD
Retinoblastoma	22278416	CNVD
Breast cancer	20953835	CNVD
oto-dental syndrome	17656375	CNVD
Asthma	21956041	CNVD
Breast cancer	17603634	CNVD
Ovarian neoplasms	16753589	CNVD
Non-small cell lung cancer	20864512	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cervical cancer	21062161	CNVD
Breast cancer	21509527	CNVD
Breast cancer	17001317	CNVD
Oral squamous cell carcinoma	16619035	CNVD
Intracranial aneurysm	16715129	CNVD
Colorectal cancer	16272173	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Colorectal cancer	16882699	CNVD
Berardinelli-seip congenital generalized lipodystrophy	17668395	CNVD
Spinal muscular atrophy	17668395	CNVD
Neonatal seizures	17668395	CNVD
Neonatal seizures	17668391	CNVD
Neuroticism	17667963	CNVD
Cancer	17916600	CNVD
Squamous cell cancer	19047905	CNVD
Multiple endocrine neoplasia type 1	19566914	CNVD
XY sex reversal	17503084	CNVD
Berardinelli-seip congenital generalized lipodystrophy	17668391	CNVD
Maculopathy	17646752	CNVD
Breast cancer	17899364	CNVD
Breast cancer	17157792	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Breast cancer	21364760	CNVD
lymphocytic leukemia	21291569	CNVD
Myelofibrosis	22110671	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Cancer	22183965	CNVD
Melanoma	22183965	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Breast cancer	16620391	CNVD
Multiple myeloma	17550852	CNVD
Neuroblastoma	18923191	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Multiple myeloma	16616336	CNVD
Urothelial cell carcinoma	18451213	CNVD
Leukoplakia	24403051	CNVD
Prostate cancer	17217626	CNVD
Cancer	22429812	CNVD
small cell lung cancer	20016488	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Breast cancer	17142309	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:407 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:71491600-71497200	Weak transcription	Rectal Mucosa Donor 31	rectum
2	chr11:71492200-71497200	Weak transcription	Stomach Mucosa	stomach
3	chr11:71493400-71497200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr11:71493600-71497200	Weak transcription	Colonic Mucosa	Colon
5	chr11:71493800-71497400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
6	chr11:71494000-71497000	Weak transcription	Duodenum Mucosa	Duodenum
7	chr11:71494000-71497200	Weak transcription	HUES6 Cell Line	embryonic stem cell
8	chr11:71494000-71497400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr11:71494400-71497200	Weak transcription	HepG2	liver
10	chr11:71494400-71497200	Weak transcription	K562	blood
11	chr11:71494600-71497200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
12	chr11:71494800-71497200	Weak transcription	Muscle Satellite Cultured Cells	--
13	chr11:71494800-71497400	Weak transcription	NHLF	lung
14	chr11:71495000-71497200	Weak transcription	Hela-S3	cervix
15	chr11:71495400-71497200	Weak transcription	Stomach Smooth Muscle	stomach
16	chr11:71495600-71497200	Enhancers	Fetal Intestine Small	intestine
17	chr11:71496000-71497200	Enhancers	Fetal Intestine Large	intestine
18	chr11:71496600-71497200	Enhancers	Rectal Mucosa Donor 29	rectum
19	chr11:71496800-71497200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
20	chr11:71496800-71499200	Active TSS	ES-I3 Cell Line	embryonic stem cell
21	chr11:71497000-71497200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
22	chr11:71497000-71497200	Enhancers	Primary B cells from peripheral blood	blood
23	chr11:71497000-71497200	Enhancers	Primary T cells fromperipheralblood	blood
24	chr11:71497000-71497200	Enhancers	Primary T helper cells PMA-I stimulated	--
25	chr11:71497000-71497200	Enhancers	Primary T helper cells fromperipheralblood	blood
26	chr11:71497000-71497200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
27	chr11:71497000-71497200	Enhancers	Adipose Nuclei	Adipose
28	chr11:71497000-71497200	Weak transcription	Brain Angular Gyrus	brain
29	chr11:71497000-71497200	Enhancers	Duodenum Mucosa	Duodenum
30	chr11:71497000-71497200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
31	chr11:71497000-71497200	Enhancers	Fetal Muscle Trunk	muscle
32	chr11:71497000-71497200	Enhancers	Fetal Muscle Leg	muscle
33	chr11:71497000-71497400	Enhancers	Primary monocytes fromperipheralblood	blood
34	chr11:71497000-71499400	Active TSS	Breast Myoepithelial Primary Cells	Breast
35	chr11:71497200-71497400	Active TSS	Primary B cells from cord blood	blood
36	chr11:71497200-71497400	Enhancers	Primary T cells from cord blood	blood
37	chr11:71497200-71497400	Enhancers	Primary hematopoietic stem cells short term culture	blood
38	chr11:71497200-71497400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
39	chr11:71497200-71497400	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
40	chr11:71497200-71497400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
41	chr11:71497200-71497400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
42	chr11:71497200-71497400	Enhancers	Muscle Satellite Cultured Cells	--
43	chr11:71497200-71497400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
44	chr11:71497200-71497400	Enhancers	Liver	Liver
45	chr11:71497200-71497400	Flanking Active TSS	Brain Angular Gyrus	brain
46	chr11:71497200-71497400	Enhancers	Brain Inferior Temporal Lobe	brain
47	chr11:71497200-71497400	Enhancers	Brain Substantia Nigra	brain
48	chr11:71497200-71497400	Active TSS	Colonic Mucosa	Colon
49	chr11:71497200-71497400	Enhancers	Placenta	Placenta
50	chr11:71497200-71497400	Flanking Active TSS	Fetal Stomach	stomach

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