Variant report

Variant	esv3439941
Chromosome Location	chr11:65373801-65376349
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr11:65374551-65374968	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr11:65374376-65375215	H1-hESC	embryonic stem cell:	n/a	n/a
3	CCNT2	chr11:65374653-65374766	K562	blood:	n/a	chr11:65374691-65374700
4	CEBPB	chr11:65374674-65374832	H1-hESC	embryonic stem cell:	n/a	n/a
5	CHD2	chr11:65374522-65375256	H1-hESC	embryonic stem cell:	n/a	n/a
6	CREB1	chr11:65374468-65375130	ECC-1	luminal epithelium:	n/a	n/a
7	CREB1	chr11:65374596-65375185	H1-hESC	embryonic stem cell:	n/a	n/a
8	CREB1	chr11:65374300-65375249	H1-hESC	embryonic stem cell:	n/a	n/a
9	CTCF	chr11:65374940-65375090	SK-N-SH_RA	brain:	n/a	n/a
10	CTCF	chr11:65374860-65375010	Caco-2	colon:	n/a	n/a
11	CTCF	chr11:65374980-65375130	Caco-2	colon:	n/a	n/a
12	CTCF	chr11:65374880-65375030	SAEC	small airway:	n/a	n/a
13	CTCF	chr11:65375040-65375190	HRE	kidney:	n/a	n/a
14	CTCF	chr11:65375000-65375150	HA-sp	spinal cord:	n/a	n/a
15	E2F6	chr11:65374508-65375420	H1-hESC	embryonic stem cell:	n/a	n/a
16	E2F6	chr11:65374370-65375653	H1-hESC	embryonic stem cell:	n/a	chr11:65374472-65374482 chr11:65374482-65374492
17	EGR1	chr11:65374439-65374947	ECC-1	luminal epithelium:	n/a	chr11:65374686-65374699 chr11:65374691-65374706 chr11:65374693-65374703 chr11:65374692-65374705 chr11:65374692-65374705 chr11:65374693-65374702 chr11:65374692-65374705 chr11:65374486-65374496
18	EGR1	chr11:65374451-65374781	K562	blood:	n/a	chr11:65374686-65374699 chr11:65374691-65374706 chr11:65374693-65374703 chr11:65374692-65374705 chr11:65374692-65374705 chr11:65374693-65374702 chr11:65374692-65374705 chr11:65374486-65374496
19	EGR1	chr11:65374405-65374816	K562	blood:	n/a	chr11:65374686-65374699 chr11:65374691-65374706 chr11:65374693-65374703 chr11:65374692-65374705 chr11:65374692-65374705 chr11:65374693-65374702 chr11:65374692-65374705 chr11:65374486-65374496
20	EP300	chr11:65374463-65375215	ECC-1	luminal epithelium:	n/a	n/a
21	FOXP2	chr11:65374418-65374950	SK-N-MC	brain:	n/a	n/a
22	GABPA	chr11:65374647-65375251	H1-hESC	embryonic stem cell:	n/a	n/a
23	GABPA	chr11:65374670-65375176	H1-hESC	embryonic stem cell:	n/a	n/a
24	GTF2F1	chr11:65374686-65375060	H1-hESC	embryonic stem cell:	n/a	n/a
25	HDAC2	chr11:65374391-65374724	H1-hESC	embryonic stem cell:	n/a	n/a
26	HMGN3	chr11:65374765-65374808	K562	blood:	n/a	n/a
27	IRF1	chr11:65374442-65374737	K562	blood:	n/a	chr11:65374681-65374695 chr11:65374599-65374613 chr11:65374483-65374497 chr11:65374702-65374711
28	JUN	chr11:65375267-65375275	H1-hESC	embryonic stem cell:	n/a	n/a
29	JUND	chr11:65374642-65374907	H1-hESC	embryonic stem cell:	n/a	n/a
30	JUND	chr11:65375205-65375207	H1-hESC	embryonic stem cell:	n/a	n/a
31	JUND	chr11:65374610-65374867	H1-hESC	embryonic stem cell:	n/a	n/a
32	MAX	chr11:65374640-65374865	K562	blood:	n/a	n/a
33	MAX	chr11:65374567-65375076	HUVEC	blood vessel:	n/a	n/a
34	MAX	chr11:65374471-65375310	H1-hESC	embryonic stem cell:	n/a	chr11:65374486-65374496
35	MAX	chr11:65374397-65375399	ECC-1	luminal epithelium:	n/a	chr11:65374486-65374496
36	MAX	chr11:65374648-65375227	H1-hESC	embryonic stem cell:	n/a	n/a
37	MAX	chr11:65374452-65375189	SK-N-SH	brain:	n/a	chr11:65374486-65374496
38	MAX	chr11:65374456-65375318	ECC-1	luminal epithelium:	n/a	chr11:65374486-65374496
39	MAX	chr11:65374412-65375371	H1-hESC	embryonic stem cell:	n/a	chr11:65374486-65374496
40	MAX	chr11:65374528-65375057	SK-N-SH	brain:	n/a	n/a
41	MAX	chr11:65374357-65375276	HCT-116	colon:	n/a	chr11:65374486-65374496
42	MAX	chr11:65374299-65375256	HCT-116	colon:	n/a	chr11:65374486-65374496
43	MAZ	chr11:65374253-65375213	IMR90	lung:	n/a	chr11:65374486-65374496
44	MXI1	chr11:65373835-65375875	SK-N-SH	brain:	n/a	n/a
45	MXI1	chr11:65374631-65375027	H1-hESC	embryonic stem cell:	n/a	n/a
46	MXI1	chr11:65374054-65375313	IMR90	lung:	n/a	n/a
47	MYC	chr11:65374735-65374850	HUVEC	blood vessel:	n/a	n/a
48	MYC	chr11:65374460-65375073	H1-hESC	embryonic stem cell:	n/a	chr11:65374486-65374496
49	NANOG	chr11:65374592-65374922	H1-hESC	embryonic stem cell:	n/a	n/a
50	NFIC	chr11:65374550-65375200	ECC-1	luminal epithelium:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:65375704-65375754	ovcar-3	ovarian:	n/a
2	chr11:65374833-65374883	HMEC	breast:	n/a
3	chr11:65374955-65375005	HMEC	breast:	n/a
4	chr11:65375704-65375754	ovcar-3	ovarian:	n/a
5	chr11:65374833-65374883	HMEC	breast:	n/a
6	chr11:65374955-65375005	HMEC	breast:	n/a
7	chr11:65374663-65374713	Hepatocyte	liver:	n/a
8	chr11:65375067-65375117	AoSMC	blood vessel:	n/a
9	chr11:65374955-65375005	HAEpiC	amniotic membrane:	n/a
10	chr11:65374955-65375005	H1-hESC	embryonic stem cell:	embryo
11	chr11:65375193-65375243	HAEpiC	amniotic membrane:	n/a
12	chr11:65374955-65375005	NHDF-neo	bronchial:	n/a
13	chr11:65375067-65375117	HUVEC	blood vessel:	n/a
14	chr11:65375193-65375243	AG10803	skin:	n/a
15	chr11:65375193-65375243	AG04449	skin:	fetal
16	chr11:65375203-65375253	Jurkat	blood:	n/a
17	chr11:65375203-65375253	ECC-1	luminal epithelium:	n/a
18	chr11:65375704-65375754	NH-A	brain:	n/a
19	chr11:65374955-65375005	AoSMC	blood vessel:	n/a
20	chr11:65374833-65374883	HCT-116	colon:	n/a
21	chr11:65374833-65374883	ovcar-3	ovarian:	n/a
22	chr11:65374663-65374713	ECC-1	luminal epithelium:	n/a
23	chr11:65374955-65375005	K562	blood:	n/a
24	chr11:65375067-65375117	Hela-S3	cervix:	n/a
25	chr11:65375704-65375754	AoSMC	blood vessel:	n/a
26	chr11:65374833-65374883	AG04449	skin:	fetal
27	chr11:65375704-65375754	HCM	heart:	n/a
28	chr11:65374955-65375005	HNPCEpiC	eye:	n/a
29	chr11:65375193-65375243	NB4	blood:	n/a
30	chr11:65375704-65375754	IMR90	lung:	fetal
31	chr11:65375704-65375754	SK-N-SH_RA	brain:	n/a
32	chr11:65375203-65375253	CMK	blood:	n/a
33	chr11:65374955-65375005	PFSK-1	brain:	n/a
34	chr11:65375067-65375117	MCF10A-Er-Src	breast:	n/a
35	chr11:65374955-65375005	AG10803	skin:	n/a
36	chr11:65375193-65375243	Caco-2	colon:	n/a
37	chr11:65374955-65375005	AG04449	skin:	fetal
38	chr11:65374833-65374883	HRE	kidney:	n/a
39	chr11:65375193-65375243	K562	blood:	n/a
40	chr11:65374663-65374713	Caco-2	colon:	n/a
41	chr11:65375704-65375754	SKMC	muscle:	n/a
42	chr11:65375193-65375243	SAEC	small airway:	n/a
43	chr11:65375704-65375754	HPAEpiC	pulmonary alveolar:	n/a
44	chr11:65375067-65375117	Hepatocyte	liver:	n/a
45	chr11:65375067-65375117	PrEC	prostate:	n/a
46	chr11:65375704-65375754	T-47D	breast:	n/a
47	chr11:65375704-65375754	HUVEC	blood vessel:	n/a
48	chr11:65374833-65374883	GM12891	blood:	n/a
49	chr11:65375067-65375117	MCF-7	breast:	n/a
50	chr11:65375704-65375754	HEK293	kidney:	embryo

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr11:65341009..65346216-chr11:65370852..65374605,4	K562	blood:
2	chr11:65336061..65346997-chr11:65371025..65390625,42	MCF-7	breast:

Variant related genes	Relation type
MAP3K11	TF binding region
MAP3K11	CpG island
ENSG00000176973	chromatin interactions
ENSG00000260233	chromatin interactions
ENSG00000173465	chromatin interactions
ENSG00000173442	chromatin interactions

Extended variants
information (count: 109 )
Associated
traits (count: 100 )

Variant overlapped rSNPs/rCNVs (count:109 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11227238	chr11:65373818-65373819	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs575946415	chr11:65373820-65373821	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs374511571	chr11:65373844-65373845	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs549976878	chr11:65373874-65373875	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
5	rs367624099	chr11:65373901-65373902	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
6	rs1679085	chr11:65373924-65373925	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
7	rs551980326	chr11:65373952-65373953	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
8	rs112629622	chr11:65373976-65373977	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
9	rs80068959	chr11:65373985-65373986	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
10	rs556073656	chr11:65373999-65374000	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
11	rs565633203	chr11:65374019-65374020	Weak transcription Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
12	rs146966484	chr11:65374029-65374030	Weak transcription Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
13	rs554852996	chr11:65374048-65374049	Weak transcription Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
14	rs567936993	chr11:65374061-65374062	Weak transcription Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
15	rs537066174	chr11:65374067-65374068	Weak transcription Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
16	rs557077431	chr11:65374072-65374073	Weak transcription Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
17	rs376567112	chr11:65374125-65374126	Weak transcription Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
18	rs577044473	chr11:65374133-65374134	Weak transcription Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
19	rs11824024	chr11:65374145-65374146	Weak transcription Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs559237415	chr11:65374283-65374284	Active TSS Enhancers Genic enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
21	rs373743021	chr11:65374291-65374292	Active TSS Enhancers Genic enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
22	rs373978204	chr11:65374325-65374326	Active TSS Enhancers Genic enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
23	rs566348393	chr11:65374329-65374330	Active TSS Enhancers Genic enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
24	rs545517734	chr11:65374357-65374358	Active TSS Enhancers Genic enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
25	rs541315313	chr11:65374387-65374388	Active TSS Enhancers Genic enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
26	rs148137861	chr11:65374392-65374393	Active TSS Enhancers Genic enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
27	rs113324277	chr11:65374400-65374401	Active TSS Enhancers Genic enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
28	rs574705603	chr11:65374423-65374424	Active TSS Enhancers Genic enhancers Strong transcription Transcr. at gene 5' and 3' Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
29	rs181247930	chr11:65374454-65374455	Active TSS Enhancers Genic enhancers Strong transcription Transcr. at gene 5' and 3' Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
30	rs563419653	chr11:65374455-65374456	Active TSS Enhancers Genic enhancers Strong transcription Transcr. at gene 5' and 3' Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
31	rs374524526	chr11:65374456-65374457	Active TSS Enhancers Genic enhancers Strong transcription Transcr. at gene 5' and 3' Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
32	rs532515949	chr11:65374479-65374480	Active TSS Enhancers Genic enhancers Strong transcription Transcr. at gene 5' and 3' Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
33	rs2306361	chr11:65374495-65374496	Active TSS Enhancers Genic enhancers Strong transcription Transcr. at gene 5' and 3' Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs559076384	chr11:65374506-65374507	Active TSS Enhancers Genic enhancers Strong transcription Transcr. at gene 5' and 3' Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
35	rs529043415	chr11:65374512-65374513	Active TSS Enhancers Genic enhancers Strong transcription Transcr. at gene 5' and 3' Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
36	rs2306360	chr11:65374538-65374539	Active TSS Enhancers Genic enhancers Strong transcription Transcr. at gene 5' and 3' Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs548151677	chr11:65374547-65374548	Active TSS Enhancers Genic enhancers Strong transcription Transcr. at gene 5' and 3' Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
38	rs372293005	chr11:65374642-65374643	Active TSS Enhancers Genic enhancers Strong transcription Transcr. at gene 5' and 3' Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
39	rs536622736	chr11:65374663-65374664	Active TSS Enhancers Genic enhancers Strong transcription Transcr. at gene 5' and 3' Weak transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
40	rs550646265	chr11:65374667-65374668	Active TSS Enhancers Genic enhancers Strong transcription Transcr. at gene 5' and 3' Weak transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
41	rs570554901	chr11:65374805-65374806	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription Genic enhancers Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
42	rs374000482	chr11:65374820-65374821	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription Genic enhancers Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
43	rs539502369	chr11:65374832-65374833	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription Genic enhancers Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
44	rs186746836	chr11:65374902-65374903	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription Genic enhancers Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
45	rs553105616	chr11:65374955-65374956	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription Genic enhancers Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
46	rs572517730	chr11:65374964-65374965	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription Genic enhancers Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
47	rs535233157	chr11:65374976-65374977	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription Genic enhancers Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
48	rs554945636	chr11:65375145-65375146	Active TSS Enhancers Transcr. at gene 5' and 3' Genic enhancers Strong transcription Flanking Active TSS Weak transcription ZNF genes & repeats	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
49	rs375814282	chr11:65375185-65375186	Active TSS Enhancers Transcr. at gene 5' and 3' Genic enhancers Strong transcription Flanking Active TSS Weak transcription ZNF genes & repeats	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
50	rs374611372	chr11:65375221-65375222	Bivalent/Poised TSS Enhancers Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Active TSS Strong transcription Flanking Bivalent TSS/Enh Weak transcription	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:100)

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
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Pituitary adenoma	18645599	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	21080181	CNVD
Smith-Lemli-Opitz syndrome	21572526	CNVD
Multiple myeloma	16461302	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Metanephric adenoma	20802469	CNVD
Chordoma	21602918	CNVD
Melanoma	18172304	CNVD
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
ovarian endometriomas	16273235	CNVD
Breast cancer	16417655	CNVD
Myelofibrosis	22110671	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Prostate cancer	17217626	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Breast cancer	21045282	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
Anaplastic thyroid cancer	18753363	CNVD
Prostate cancer	18779856	CNVD
Cancer	17160897	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
Chronic lymphocytic leukemia	22228453	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:444 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:65356800-65376400	Strong transcription	Primary neutrophils fromperipheralblood	blood
2	chr11:65361000-65374000	Weak transcription	Fetal Brain Male	brain
3	chr11:65361200-65374200	Strong transcription	Fetal Intestine Small	intestine
4	chr11:65362200-65379800	Weak transcription	Pancreatic Islets	Pancreatic Islet
5	chr11:65362800-65374000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
6	chr11:65363400-65374000	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
7	chr11:65363600-65374000	Weak transcription	Fetal Heart	heart
8	chr11:65363600-65374000	Strong transcription	Fetal Stomach	stomach
9	chr11:65363600-65374200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr11:65363600-65375000	Strong transcription	Thymus	Thymus
11	chr11:65363600-65376800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
12	chr11:65363800-65376600	Strong transcription	Monocytes-CD14+_RO01746	blood
13	chr11:65364000-65374000	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
14	chr11:65364000-65374000	Strong transcription	Fetal Muscle Leg	muscle
15	chr11:65364000-65374000	Strong transcription	Lung	lung
16	chr11:65364000-65374800	Strong transcription	Fetal Intestine Large	intestine
17	chr11:65364000-65376600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
18	chr11:65364000-65378000	Weak transcription	K562	blood
19	chr11:65364200-65378400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr11:65364800-65376800	Strong transcription	Primary hematopoietic stem cells short term culture	blood
21	chr11:65365000-65374000	Strong transcription	Adipose Nuclei	Adipose
22	chr11:65365000-65374200	Strong transcription	Fetal Thymus	thymus
23	chr11:65365000-65374200	Strong transcription	Rectal Mucosa Donor 29	rectum
24	chr11:65365000-65374800	Strong transcription	Liver	Liver
25	chr11:65365000-65376800	Strong transcription	Primary monocytes fromperipheralblood	blood
26	chr11:65366000-65374200	Weak transcription	Psoas Muscle	Psoas
27	chr11:65366600-65374200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
28	chr11:65366600-65374200	Weak transcription	Stomach Mucosa	stomach
29	chr11:65366600-65377600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
30	chr11:65367600-65374200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
31	chr11:65369600-65376600	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
32	chr11:65369800-65374200	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
33	chr11:65369800-65375200	Strong transcription	Rectal Mucosa Donor 31	rectum
34	chr11:65369800-65377000	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
35	chr11:65369800-65377800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
36	chr11:65370000-65374200	Strong transcription	Right Ventricle	heart
37	chr11:65370200-65374200	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
38	chr11:65370200-65374200	Strong transcription	Brain Substantia Nigra	brain
39	chr11:65370200-65374200	Strong transcription	Duodenum Mucosa	Duodenum
40	chr11:65370200-65374800	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
41	chr11:65370200-65376200	Strong transcription	Pancreas	Pancrea
42	chr11:65370200-65376800	Strong transcription	Primary T helper cells fromperipheralblood	blood
43	chr11:65370400-65377000	Strong transcription	Primary T cells from cord blood	blood
44	chr11:65370400-65377000	Strong transcription	Primary T cells fromperipheralblood	blood
45	chr11:65370400-65377400	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
46	chr11:65370400-65377400	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
47	chr11:65370400-65377600	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
48	chr11:65370600-65374000	Strong transcription	Brain Cingulate Gyrus	brain
49	chr11:65370600-65374000	Strong transcription	NH-A	brain
50	chr11:65370600-65374200	Strong transcription	Brain Inferior Temporal Lobe	brain

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