Variant report

Variant	esv1850719
Chromosome Location	chr11:36616867-36657272
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	ARID3A	chr11:36634803-36634844	K562	blood:	n/a	n/a
2	ARID3A	chr11:36639666-36639932	K562	blood:	n/a	n/a
3	ATF1	chr11:36639616-36640021	K562	blood:	n/a	n/a
4	ATF1	chr11:36644356-36644640	K562	blood:	n/a	n/a
5	ATF1	chr11:36654986-36654995	K562	blood:	n/a	n/a
6	ATF1	chr11:36622845-36623044	K562	blood:	n/a	n/a
7	BHLHE40	chr11:36627458-36627611	GM12878	blood:	n/a	n/a
8	CCNT2	chr11:36631495-36631695	K562	blood:	n/a	n/a
9	CEBPB	chr11:36644359-36644647	Hela-S3	cervix:	n/a	n/a
10	CEBPB	chr11:36645242-36645533	IMR90	lung:	n/a	n/a
11	CEBPB	chr11:36645274-36645554	HepG2	liver:	n/a	n/a
12	CREB1	chr11:36653205-36653599	GM12878	blood:	n/a	n/a
13	CTCF	chr11:36644460-36644610	GM12865	blood:	n/a	chr11:36644502-36644515 chr11:36644495-36644516 chr11:36644500-36644518 chr11:36644506-36644515
14	CTCF	chr11:36644424-36644597	GM13977	blood:	n/a	chr11:36644502-36644515 chr11:36644495-36644516 chr11:36644500-36644518 chr11:36644506-36644515
15	CTCF	chr11:36644460-36644610	HMEC	breast:	n/a	chr11:36644502-36644515 chr11:36644495-36644516 chr11:36644500-36644518 chr11:36644506-36644515
16	CTCF	chr11:36644440-36644590	HBMEC	blood vessel:	n/a	chr11:36644502-36644515 chr11:36644495-36644516 chr11:36644500-36644518 chr11:36644506-36644515
17	CTCF	chr11:36644380-36644530	WERI-Rb-1	eye:	n/a	chr11:36644502-36644515 chr11:36644495-36644516 chr11:36644500-36644518 chr11:36644506-36644515
18	CTCF	chr11:36644420-36644570	HepG2	liver:	n/a	chr11:36644502-36644515 chr11:36644495-36644516 chr11:36644500-36644518 chr11:36644506-36644515
19	CTCF	chr11:36644420-36644570	GM12866	blood:	n/a	chr11:36644502-36644515 chr11:36644495-36644516 chr11:36644500-36644518 chr11:36644506-36644515
20	CTCF	chr11:36644440-36644590	HCM	heart:	n/a	chr11:36644502-36644515 chr11:36644495-36644516 chr11:36644500-36644518 chr11:36644506-36644515
21	CTCF	chr11:36644460-36644610	AG09309	skin:	n/a	chr11:36644502-36644515 chr11:36644495-36644516 chr11:36644500-36644518 chr11:36644506-36644515
22	CTCF	chr11:36644440-36644590	HRPEpiC	eye:	n/a	chr11:36644502-36644515 chr11:36644495-36644516 chr11:36644500-36644518 chr11:36644506-36644515
23	CTCF	chr11:36644480-36644630	HRE	kidney:	n/a	chr11:36644502-36644515 chr11:36644495-36644516 chr11:36644500-36644518 chr11:36644506-36644515
24	CTCF	chr11:36644017-36644791	A549	lung:	n/a	chr11:36644502-36644515 chr11:36644495-36644516 chr11:36644500-36644518 chr11:36644506-36644515
25	CTCF	chr11:36644420-36644570	BJ	skin:	n/a	chr11:36644502-36644515 chr11:36644495-36644516 chr11:36644500-36644518 chr11:36644506-36644515
26	CTCF	chr11:36644340-36644490	HCM	heart:	n/a	n/a
27	CTCF	chr11:36644419-36644601	GM10248	blood:	n/a	chr11:36644502-36644515 chr11:36644495-36644516 chr11:36644500-36644518 chr11:36644506-36644515
28	CTCF	chr11:36644420-36644570	HRPEpiC	eye:	n/a	chr11:36644502-36644515 chr11:36644495-36644516 chr11:36644500-36644518 chr11:36644506-36644515
29	CTCF	chr11:36644409-36644603	SK-N-SH_RA	brain:	n/a	chr11:36644502-36644515 chr11:36644495-36644516 chr11:36644500-36644518 chr11:36644506-36644515
30	CTCF	chr11:36644420-36644570	SK-N-SH_RA	brain:	n/a	chr11:36644502-36644515 chr11:36644495-36644516 chr11:36644500-36644518 chr11:36644506-36644515
31	CTCF	chr11:36644460-36644610	GM12864	blood:	n/a	chr11:36644502-36644515 chr11:36644495-36644516 chr11:36644500-36644518 chr11:36644506-36644515
32	CTCF	chr11:36644389-36644639	Gliobla	brain:	n/a	chr11:36644502-36644515 chr11:36644495-36644516 chr11:36644500-36644518 chr11:36644506-36644515
33	CTCF	chr11:36644400-36644550	HA-sp	spinal cord:	n/a	chr11:36644502-36644515 chr11:36644495-36644516 chr11:36644500-36644518 chr11:36644506-36644515
34	CTCF	chr11:36644400-36644550	NHEK	skin:	n/a	chr11:36644502-36644515 chr11:36644495-36644516 chr11:36644500-36644518 chr11:36644506-36644515
35	CTCF	chr11:36644440-36644590	HFF	foreskin:	n/a	chr11:36644502-36644515 chr11:36644495-36644516 chr11:36644500-36644518 chr11:36644506-36644515
36	CTCF	chr11:36644430-36644567	A549	lung:	n/a	chr11:36644502-36644515 chr11:36644495-36644516 chr11:36644500-36644518 chr11:36644506-36644515
37	CTCF	chr11:36644420-36644570	HVMF	connective:	n/a	chr11:36644502-36644515 chr11:36644495-36644516 chr11:36644500-36644518 chr11:36644506-36644515
38	CTCF	chr11:36644431-36644613	ProgFib	skin:	n/a	chr11:36644502-36644515 chr11:36644495-36644516 chr11:36644500-36644518 chr11:36644506-36644515
39	CTCF	chr11:36644440-36644590	HEK293	kidney:	n/a	chr11:36644502-36644515 chr11:36644495-36644516 chr11:36644500-36644518 chr11:36644506-36644515
40	CTCF	chr11:36644460-36644610	HPAF	blood vessel:	n/a	chr11:36644502-36644515 chr11:36644495-36644516 chr11:36644500-36644518 chr11:36644506-36644515
41	CTCF	chr11:36644440-36644590	AG09319	gingival:	n/a	chr11:36644502-36644515 chr11:36644495-36644516 chr11:36644500-36644518 chr11:36644506-36644515
42	CTCF	chr11:36644411-36644641	LNCaP	prostate:	n/a	chr11:36644502-36644515 chr11:36644495-36644516 chr11:36644500-36644518 chr11:36644506-36644515
43	CTCF	chr11:36644340-36644490	HAc	cerebellar:	n/a	n/a
44	CTCF	chr11:36644420-36644570	GM12864	blood:	n/a	chr11:36644502-36644515 chr11:36644495-36644516 chr11:36644500-36644518 chr11:36644506-36644515
45	CTCF	chr11:36644480-36644630	GM12865	blood:	n/a	chr11:36644502-36644515 chr11:36644495-36644516 chr11:36644500-36644518 chr11:36644506-36644515
46	CTCF	chr11:36644350-36644588	T-47D	breast:	n/a	chr11:36644502-36644515 chr11:36644495-36644516 chr11:36644500-36644518 chr11:36644506-36644515
47	CTCF	chr11:36644400-36644550	HMF	breast:	n/a	chr11:36644502-36644515 chr11:36644495-36644516 chr11:36644500-36644518 chr11:36644506-36644515
48	CTCF	chr11:36644420-36644570	AoAF	blood vessel:	n/a	chr11:36644502-36644515 chr11:36644495-36644516 chr11:36644500-36644518 chr11:36644506-36644515
49	CTCF	chr11:36644380-36644530	Hela-S3	cervix:	n/a	chr11:36644502-36644515 chr11:36644495-36644516 chr11:36644500-36644518 chr11:36644506-36644515
50	CTCF	chr11:36644460-36644610	HFF-Myc	foreskin:	n/a	chr11:36644502-36644515 chr11:36644495-36644516 chr11:36644500-36644518 chr11:36644506-36644515

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:36620443-36620493	HCT-116	colon:	n/a
2	chr11:36620443-36620493	HRCEpiC	kidney:	n/a
3	chr11:36620443-36620493	SKMC	muscle:	n/a
4	chr11:36619694-36619744	SK-N-SH	brain:	n/a
5	chr11:36620443-36620493	HepG2	liver:	n/a
6	chr11:36619694-36619744	NHBE	bronchial:	n/a
7	chr11:36620199-36620249	NB4	blood:	n/a
8	chr11:36652206-36652256	CMK	blood:	n/a
9	chr11:36652206-36652256	AoSMC	blood vessel:	n/a
10	chr11:36652206-36652256	AG09309	skin:	n/a
11	chr11:36619694-36619744	HNPCEpiC	eye:	n/a
12	chr11:36620443-36620493	AoSMC	blood vessel:	n/a
13	chr11:36619694-36619744	HIPEpiC	eye:	n/a
14	chr11:36620443-36620493	U87	brain:	n/a
15	chr11:36652206-36652256	PrEC	prostate:	n/a
16	chr11:36620443-36620493	NHDF-neo	bronchial:	n/a
17	chr11:36620443-36620493	A549	lung:	n/a
18	chr11:36619694-36619744	HMEC	breast:	n/a
19	chr11:36620443-36620493	AG04449	skin:	fetal
20	chr11:36620443-36620493	MCF-7	breast:	n/a
21	chr11:36620199-36620249	HNPCEpiC	eye:	n/a
22	chr11:36652206-36652256	Jurkat	blood:	n/a
23	chr11:36619694-36619744	HCT-116	colon:	n/a
24	chr11:36652206-36652256	K562	blood:	n/a
25	chr11:36652206-36652256	GM12892	blood:	n/a
26	chr11:36619694-36619744	ProgFib	skin:	n/a
27	chr11:36620443-36620493	IMR90	lung:	fetal
28	chr11:36620443-36620493	AG09309	skin:	n/a
29	chr11:36620443-36620493	HCF	heart:	n/a
30	chr11:36619694-36619744	AG09319	gingival:	n/a
31	chr11:36620199-36620249	ECC-1	luminal epithelium:	n/a
32	chr11:36652206-36652256	PFSK-1	brain:	n/a
33	chr11:36620443-36620493	GM12892	blood:	n/a
34	chr11:36619694-36619744	GM12878	blood:	n/a
35	chr11:36652206-36652256	ovcar-3	ovarian:	n/a
36	chr11:36619694-36619744	HEK293	kidney:	embryo
37	chr11:36652206-36652256	H1-hESC	embryonic stem cell:	embryo
38	chr11:36652206-36652256	BJ	skin:	n/a
39	chr11:36652206-36652256	Caco-2	colon:	n/a
40	chr11:36652206-36652256	AG10803	skin:	n/a
41	chr11:36652206-36652256	ECC-1	luminal epithelium:	n/a
42	chr11:36652206-36652256	AG04450	lung:	fetal
43	chr11:36652206-36652256	SK-N-SH	brain:	n/a
44	chr11:36620443-36620493	LNCaP	prostate:	n/a
45	chr11:36619694-36619744	NB4	blood:	n/a
46	chr11:36620443-36620493	GM12891	blood:	n/a
47	chr11:36619694-36619744	HCPEpiC	choroid plexus:	n/a
48	chr11:36652206-36652256	GM12891	blood:	n/a
49	chr11:36619694-36619744	MCF10A-Er-Src	breast:	n/a
50	chr11:36620199-36620249	K562	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:36585345..36586221-chr11:36643988..36644896,2	K562	blood:
2	chr11:36587708..36589968-chr11:36622211..36624762,2	MCF-7	breast:
3	chr11:36585864..36586647-chr11:36643987..36644963,5	MCF-7	breast:
4	chr11:36588036..36588727-chr11:36644218..36644936,3	MCF-7	breast:
5	chr11:36642647..36644362-chr11:36665197..36666895,2	K562	blood:
6	chr11:36649743..36651991-chr11:36654545..36656846,2	MCF-7	breast:
7	chr11:36611242..36613521-chr11:36616651..36619477,2	K562	blood:
8	chr11:36649743..36651991-chr11:36654545..36656846,2	MCF-7	breast:
9	chr11:36593184..36595946-chr11:36621814..36623682,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RAG2-1	chr11:36619652-36619783	NONHSAT018834
2	lnc-RAG2-1	chr11:36619652-36619783	NONHSAT018836
3	lnc-RAG2-1	chr11:36619652-36619829	NONHSAT018835

Variant related genes	Relation type
RAG2	TF binding region
RAG2	CpG island
ENSG00000166349	chromatin interactions

Extended variants
information (count: 1468 )
Associated
traits (count: 54 )

Variant overlapped rSNPs/rCNVs (count:1468 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7104753	chr11:36616867-36616868	Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs530282520	chr11:36616876-36616877	Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
3	rs577287426	chr11:36617046-36617047	Active TSS Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
4	rs116482064	chr11:36617053-36617054	Active TSS Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
5	rs559845529	chr11:36617085-36617086	Active TSS Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs542464528	chr11:36617089-36617090	Active TSS Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs79495334	chr11:36617140-36617141	Active TSS Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs190955193	chr11:36617141-36617142	Active TSS Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs142899515	chr11:36617147-36617148	Active TSS Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs181864627	chr11:36617194-36617195	Active TSS Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
11	rs573332136	chr11:36617210-36617211	Weak transcription Active TSS Enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
12	rs146084584	chr11:36617268-36617269	Weak transcription Active TSS Enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
13	rs551513384	chr11:36617292-36617293	Weak transcription Active TSS Enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
14	rs552677313	chr11:36617301-36617302	Weak transcription Active TSS Enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
15	rs16929104	chr11:36617304-36617305	Weak transcription Active TSS Enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs111997603	chr11:36617311-36617312	Weak transcription Active TSS Enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
17	rs140146300	chr11:36617339-36617340	Weak transcription Active TSS Enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
18	rs143811003	chr11:36617354-36617355	Weak transcription Active TSS Enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs535848842	chr11:36617387-36617388	Weak transcription Active TSS Enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs555480594	chr11:36617398-36617399	Weak transcription Active TSS Enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs569495423	chr11:36617448-36617449	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
22	rs186939051	chr11:36617485-36617486	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
23	rs151292872	chr11:36617490-36617491	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
24	rs575677869	chr11:36617491-36617492	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
25	rs117211111	chr11:36617495-36617496	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
26	rs139412015	chr11:36617518-36617519	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
27	rs553439920	chr11:36617542-36617543	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
28	rs73455539	chr11:36617576-36617577	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3'	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs191186384	chr11:36617615-36617616	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
30	rs370088721	chr11:36617674-36617675	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
31	rs562350950	chr11:36617762-36617763	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
32	rs533577050	chr11:36617772-36617773	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
33	rs71047991	chr11:36617773-36617774	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
34	rs201534997	chr11:36617776-36617777	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
35	rs576251203	chr11:36617779-36617780	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
36	rs544997144	chr11:36617780-36617781	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
37	rs67282079	chr11:36617783-36617784	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
38	rs398015783	chr11:36617787-36617788	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
39	rs183088344	chr11:36617796-36617797	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
40	rs116969052	chr11:36617810-36617811	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
41	rs16929106	chr11:36617815-36617816	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3'	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs867802	chr11:36617858-36617859	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3'	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs186698719	chr11:36617873-36617874	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
44	rs73455540	chr11:36617883-36617884	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3'	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs867801	chr11:36617989-36617990	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3'	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs538268610	chr11:36617996-36617997	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
47	rs113290425	chr11:36618025-36618026	Weak transcription Active TSS Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
48	rs571650864	chr11:36618091-36618092	Weak transcription Active TSS Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
49	rs375644254	chr11:36618131-36618132	Weak transcription Active TSS Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
50	rs534121134	chr11:36618215-36618216	Weak transcription Flanking Active TSS Enhancers Active TSS Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:54)

Disease	PMID	Source
Thyroid cancer	19087340	CNVD
Melanoma	18172304	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Wilms tumour	21544195	CNVD
Parathyroid adenoma	22454399	CNVD
Medulloblastoma	21979893	CNVD
Chordoma	21602918	CNVD
Breast cancer	21949216	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	19222835	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Beckwith-Wiedemann syndrome	21518781	CNVD
Wilms tumour	21518781	CNVD
Hepatoblastoma	21518781	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Autism	22495311	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	21785460	CNVD
Medulloblastoma	16783165	CNVD
small cell lung cancer	20016488	CNVD
Renal cell carcinoma	18194544	CNVD
WAGR syndrome	19222835	CNVD
Breast cancer	17603634	CNVD
Chordoma	18071362	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Breast cancer	21364760	CNVD
Non-small cell lung cancer	21829676	CNVD
Potocki-Shaffer syndrome	19222835	CNVD
WAGR syndrome	20603712	CNVD
Autism	17322880	CNVD
Renal cell carcinoma	18765545	CNVD
Breast cancer	21858162	CNVD
Cancer	20164920	CNVD
Breast cancer	16620391	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:504 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:36614200-36617200	Transcr. at gene 5' and 3'	Thymus	Thymus
2	chr11:36614200-36619600	Transcr. at gene 5' and 3'	Dnd41	blood
3	chr11:36615600-36617000	Active TSS	K562	blood
4	chr11:36615800-36617000	Active TSS	HUES6 Cell Line	embryonic stem cell
5	chr11:36615800-36617000	Active TSS	iPS-20b Cell Line	embryonic stem cell
6	chr11:36615800-36617000	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
7	chr11:36615800-36617000	Active TSS	Primary hematopoietic stem cells short term culture	blood
8	chr11:36615800-36617000	Active TSS	Rectal Mucosa Donor 29	rectum
9	chr11:36615800-36617000	Active TSS	A549	lung
10	chr11:36615800-36617000	Active TSS	HMEC	breast
11	chr11:36615800-36617000	Active TSS	NH-A	brain
12	chr11:36615800-36617000	Active TSS	NHDF-Ad	bronchial
13	chr11:36615800-36617200	Active TSS	H1 Cell Line	embryonic stem cell
14	chr11:36615800-36617200	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
15	chr11:36616000-36617000	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
16	chr11:36616000-36617000	Active TSS	iPS-15b Cell Line	embryonic stem cell
17	chr11:36616000-36617000	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
18	chr11:36616000-36617000	Active TSS	Breast Myoepithelial Primary Cells	Breast
19	chr11:36616000-36617000	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
20	chr11:36616000-36617000	Active TSS	Duodenum Mucosa	Duodenum
21	chr11:36616000-36617000	Active TSS	Fetal Muscle Leg	muscle
22	chr11:36616000-36617000	Active TSS	Fetal Stomach	stomach
23	chr11:36616000-36617000	Active TSS	Right Ventricle	heart
24	chr11:36616000-36617200	Active TSS	HUES64 Cell Line	embryonic stem cell
25	chr11:36616000-36617200	Active TSS	Brain Germinal Matrix	brain
26	chr11:36616000-36617200	Active TSS	Psoas Muscle	Psoas
27	chr11:36616000-36617200	Active TSS	Right Atrium	heart
28	chr11:36616000-36617200	Active TSS	HSMMtube	muscle
29	chr11:36616000-36617200	Active TSS	NHLF	lung
30	chr11:36616200-36617200	Flanking Active TSS	Primary hematopoietic stem cells	blood
31	chr11:36616400-36617000	Flanking Active TSS	Adipose Nuclei	Adipose
32	chr11:36616400-36617200	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
33	chr11:36616400-36617200	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
34	chr11:36616400-36617200	Flanking Active TSS	Liver	Liver
35	chr11:36616400-36617200	Flanking Active TSS	Fetal Brain Female	brain
36	chr11:36616600-36617000	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr11:36616600-36617000	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
38	chr11:36616600-36617000	Flanking Active TSS	Primary T cells from cord blood	blood
39	chr11:36616600-36617000	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
40	chr11:36616600-36617000	Active TSS	Fetal Brain Male	brain
41	chr11:36616600-36617000	Weak transcription	Gastric	stomach
42	chr11:36616600-36617000	Active TSS	Skeletal Muscle Female	skeletal muscle
43	chr11:36616600-36617000	Active TSS	HepG2	liver
44	chr11:36616600-36617000	Flanking Active TSS	Osteobl	bone
45	chr11:36616600-36617200	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
46	chr11:36616600-36617200	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
47	chr11:36616600-36617200	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
48	chr11:36616600-36617200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
49	chr11:36616600-36617200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
50	chr11:36616600-36617200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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