Variant report

Variant	esv3376183
Chromosome Location	chr11:66334601-66337149
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:172)
CpG islands
(count:672)
Chromatin interactive
region (count:7)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:172 , 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	chr11:66336041-66336162	GM12878	blood:	n/a	n/a
2	ATF3	chr11:66335960-66336249	K562	blood:	n/a	n/a
3	BCL3	chr11:66335947-66336425	A549	lung:	n/a	chr11:66336015-66336028
4	BHLHE40	chr11:66335920-66336415	K562	blood:	n/a	n/a
5	BHLHE40	chr11:66336011-66336350	GM12878	blood:	n/a	n/a
6	BHLHE40	chr11:66336004-66336301	A549	lung:	n/a	n/a
7	CBX3	chr11:66335874-66336488	K562	blood:	n/a	n/a
8	CCNT2	chr11:66335721-66336260	K562	blood:	n/a	n/a
9	CHD2	chr11:66336107-66336111	K562	blood:	n/a	n/a
10	CREB1	chr11:66335783-66336196	A549	lung:	n/a	n/a
11	CTCF	chr11:66335440-66335590	HRPEpiC	eye:	n/a	n/a
12	CTCF	chr11:66335300-66335450	HAc	cerebellar:	n/a	n/a
13	CTCF	chr11:66335380-66335530	AG04449	skin:	n/a	n/a
14	CTCF	chr11:66335460-66335610	WERI-Rb-1	eye:	n/a	n/a
15	CTCF	chr11:66335996-66336172	Spleen_OC	spleen:	n/a	chr11:66336043-66336056
16	CTCF	chr11:66335940-66336090	AG04449	skin:	n/a	chr11:66336043-66336056
17	CTCF	chr11:66335420-66335570	HBMEC	blood vessel:	n/a	n/a
18	CTCF	chr11:66335440-66335590	SK-N-SH_RA	brain:	n/a	n/a
19	CTCF	chr11:66335480-66335630	SK-N-SH_RA	brain:	n/a	n/a
20	CTCF	chr11:66335380-66335530	HRPEpiC	eye:	n/a	n/a
21	CUX1	chr11:66336135-66336258	K562	blood:	n/a	n/a
22	E2F4	chr11:66335972-66336316	MCF10A-Er-Src	breast:	n/a	chr11:66336090-66336100 chr11:66336093-66336102
23	E2F6	chr11:66335824-66336443	A549	lung:	n/a	chr11:66336090-66336100 chr11:66336093-66336102 chr11:66336146-66336157
24	E2F6	chr11:66335934-66336329	Hela-S3	cervix:	n/a	chr11:66336090-66336100 chr11:66336093-66336102 chr11:66336146-66336157
25	E2F6	chr11:66335710-66336403	K562	blood:	n/a	chr11:66336090-66336100 chr11:66336093-66336102 chr11:66336146-66336157
26	E2F6	chr11:66335756-66336335	K562	blood:	n/a	chr11:66336090-66336100 chr11:66336093-66336102 chr11:66336146-66336157
27	E2F6	chr11:66335693-66336500	K562	blood:	n/a	chr11:66336090-66336100 chr11:66336093-66336102 chr11:66336146-66336157
28	E2F6	chr11:66335641-66336453	A549	lung:	n/a	chr11:66336090-66336100 chr11:66336093-66336102 chr11:66336146-66336157
29	EGR1	chr11:66335796-66335941	GM12878	blood:	n/a	n/a
30	EGR1	chr11:66335718-66336030	K562	blood:	n/a	n/a
31	EGR1	chr11:66335674-66336080	K562	blood:	n/a	n/a
32	ELF1	chr11:66336023-66336283	A549	lung:	n/a	n/a
33	EP300	chr11:66336043-66336283	K562	blood:	n/a	n/a
34	FOS	chr11:66336159-66336451	MCF10A-Er-Src	breast:	n/a	n/a
35	FOS	chr11:66336064-66336367	MCF10A-Er-Src	breast:	n/a	n/a
36	FOS	chr11:66336114-66336429	MCF10A-Er-Src	breast:	n/a	n/a
37	FOS	chr11:66336070-66336313	MCF10A-Er-Src	breast:	n/a	n/a
38	FOXA1	chr11:66335977-66336234	ECC-1	luminal epithelium:	n/a	n/a
39	FOXA1	chr11:66335957-66336256	ECC-1	luminal epithelium:	n/a	n/a
40	FOXA1	chr11:66335899-66336331	T-47D	breast:	n/a	n/a
41	FOXA1	chr11:66335856-66336264	T-47D	breast:	n/a	n/a
42	FOXA2	chr11:66335720-66336493	A549	lung:	n/a	n/a
43	FOXA2	chr11:66335774-66336460	A549	lung:	n/a	n/a
44	FOXP2	chr11:66335933-66336315	SK-N-MC	brain:	n/a	n/a
45	HA-E2F1	chr11:66335986-66336344	MCF-7	breast:	n/a	chr11:66336090-66336100 chr11:66336093-66336102
46	HCFC1	chr11:66336042-66336198	K562	blood:	n/a	n/a
47	HEY1	chr11:66335900-66336175	K562	blood:	n/a	chr11:66336021-66336036 chr11:66336121-66336130
48	HMGN3	chr11:66335471-66336214	K562	blood:	n/a	n/a
49	JUN	chr11:66335923-66336521	K562	blood:	n/a	n/a
50	JUND	chr11:66336024-66336436	K562	blood:	n/a	n/a

(count:672 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:66335975-66336025	NB4	blood:	n/a
2	chr11:66335975-66336025	NB4	blood:	n/a
3	chr11:66336150-66336200	NB4	blood:	n/a
4	chr11:66336197-66336247	SK-N-SH	brain:	n/a
5	chr11:66336125-66336175	Hela-S3	cervix:	n/a
6	chr11:66335649-66335699	AG10803	skin:	n/a
7	chr11:66337115-66337165	SK-N-SH	brain:	n/a
8	chr11:66335282-66335332	NB4	blood:	n/a
9	chr11:66336125-66336175	AG10803	skin:	n/a
10	chr11:66337115-66337165	PrEC	prostate:	n/a
11	chr11:66335649-66335699	BE2_C	brain:	n/a
12	chr11:66335975-66336025	AG09319	gingival:	n/a
13	chr11:66337115-66337165	AG04450	lung:	fetal
14	chr11:66336150-66336200	AG10803	skin:	n/a
15	chr11:66337115-66337165	LNCaP	prostate:	n/a
16	chr11:66336197-66336247	HAEpiC	amniotic membrane:	n/a
17	chr11:66336150-66336200	AG04450	lung:	fetal
18	chr11:66335282-66335332	A549	lung:	n/a
19	chr11:66336150-66336200	SK-N-SH_RA	brain:	n/a
20	chr11:66336293-66336343	NHDF-neo	bronchial:	n/a
21	chr11:66337115-66337165	SKMC	muscle:	n/a
22	chr11:66335649-66335699	SAEC	small airway:	n/a
23	chr11:66336132-66336182	Caco-2	colon:	n/a
24	chr11:66337111-66337161	CMK	blood:	n/a
25	chr11:66337115-66337165	AG09309	skin:	n/a
26	chr11:66336150-66336200	GM12891	blood:	n/a
27	chr11:66337111-66337161	AG09309	skin:	n/a
28	chr11:66336244-66336294	GM12892	blood:	n/a
29	chr11:66337111-66337161	SKMC	muscle:	n/a
30	chr11:66335649-66335699	CMK	blood:	n/a
31	chr11:66335282-66335332	HepG2	liver:	n/a
32	chr11:66335649-66335699	HL-60	blood:	n/a
33	chr11:66336132-66336182	K562	blood:	n/a
34	chr11:66337115-66337165	RPTEC	kidney:	n/a
35	chr11:66335649-66335699	GM12892	blood:	n/a
36	chr11:66335649-66335699	AoSMC	blood vessel:	n/a
37	chr11:66336197-66336247	GM19239	blood:	n/a
38	chr11:66337115-66337165	HEEpiC	esophagus:	n/a
39	chr11:66335649-66335699	K562	blood:	n/a
40	chr11:66336150-66336200	GM19239	blood:	n/a
41	chr11:66336150-66336200	PFSK-1	brain:	n/a
42	chr11:66336132-66336182	PANC-1	pancreas:	n/a
43	chr11:66336197-66336247	ECC-1	luminal epithelium:	n/a
44	chr11:66335649-66335699	HCF	heart:	n/a
45	chr11:66336293-66336343	HRE	kidney:	n/a
46	chr11:66336132-66336182	HPAEpiC	pulmonary alveolar:	n/a
47	chr11:66336150-66336200	HepG2	liver:	n/a
48	chr11:66335975-66336025	MCF10A-Er-Src	breast:	n/a
49	chr11:66336125-66336175	H1-hESC	embryonic stem cell:	embryo
50	chr11:66335975-66336025	NHBE	bronchial:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr11:66333833..66336382-chr11:66443152..66446114,2	MCF-7	breast:
2	chr11:66333517..66336306-chr11:66404884..66407774,3	K562	blood:
3	chr11:66333502..66335839-chr11:66382927..66384488,2	K562	blood:
4	chr11:66334662..66337726-chr11:66444588..66447609,3	K562	blood:
5	chr11:66333502..66336819-chr11:66382812..66384536,3	K562	blood:
6	chr11:66311475..66316022-chr11:66335981..66338223,4	MCF-7	breast:
7	chr11:66333513..66337489-chr11:66382854..66385992,4	MCF-7	breast:

No data

Variant related genes	Relation type
CTSF	TF binding region
CTSF	CpG island
ENSG00000173933	chromatin interactions
ENSG00000248746	chromatin interactions
ENSG00000248643	chromatin interactions
ENSG00000174165	chromatin interactions
ENSG00000173914	chromatin interactions
ENSG00000239306	chromatin interactions

Extended variants
information (count: 113 )
Associated
traits (count: 93 )

Variant overlapped rSNPs/rCNVs (count:113 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs183697819	chr11:66334612-66334613	Weak transcription Enhancers Bivalent Enhancer Strong transcription Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
2	rs370598514	chr11:66334667-66334668	Weak transcription Enhancers Bivalent Enhancer Strong transcription Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
3	rs373380286	chr11:66334684-66334685	Weak transcription Enhancers Bivalent Enhancer Strong transcription Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
4	rs577148955	chr11:66334693-66334694	Weak transcription Enhancers Bivalent Enhancer Strong transcription Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
5	rs200932066	chr11:66334727-66334728	Weak transcription Enhancers Bivalent Enhancer Strong transcription Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
6	rs143814748	chr11:66334737-66334738	Weak transcription Enhancers Bivalent Enhancer Strong transcription Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
7	rs146841814	chr11:66334741-66334742	Weak transcription Enhancers Bivalent Enhancer Strong transcription Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
8	rs202226607	chr11:66334745-66334746	Weak transcription Enhancers Bivalent Enhancer Strong transcription Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
9	rs142743244	chr11:66334757-66334758	Weak transcription Enhancers Bivalent Enhancer Strong transcription Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
10	rs140630766	chr11:66334760-66334761	Weak transcription Enhancers Bivalent Enhancer Strong transcription Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
11	rs200610855	chr11:66334763-66334764	Weak transcription Enhancers Bivalent Enhancer Strong transcription Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
12	rs528679828	chr11:66334778-66334779	Weak transcription Enhancers Bivalent Enhancer Strong transcription Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
13	rs150481606	chr11:66334787-66334788	Weak transcription Enhancers Bivalent Enhancer Strong transcription Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
14	rs548621329	chr11:66334835-66334836	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
15	rs371296361	chr11:66334837-66334838	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
16	rs562176915	chr11:66334854-66334855	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
17	rs374291363	chr11:66334868-66334869	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
18	rs200050648	chr11:66334869-66334870	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
19	rs527638704	chr11:66334873-66334874	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
20	rs372789274	chr11:66334884-66334885	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
21	rs150926626	chr11:66334912-66334913	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
22	rs369416976	chr11:66334954-66334955	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
23	rs372121871	chr11:66334973-66334974	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
24	rs11550508	chr11:66334988-66334989	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
25	rs376744562	chr11:66334996-66334997	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
26	rs149140177	chr11:66335026-66335027	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
27	rs79274952	chr11:66335028-66335029	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
28	rs267603129	chr11:66335052-66335053	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
29	rs368340392	chr11:66335081-66335082	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
30	rs369135126	chr11:66335084-66335085	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
31	rs372604212	chr11:66335091-66335092	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
32	rs112809338	chr11:66335095-66335096	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
33	rs372677922	chr11:66335116-66335117	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
34	rs201601493	chr11:66335146-66335147	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
35	rs377214961	chr11:66335160-66335161	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
36	rs535300071	chr11:66335180-66335181	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
37	rs555011410	chr11:66335233-66335234	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
38	rs568634525	chr11:66335258-66335259	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
39	rs537428419	chr11:66335272-66335273	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
40	rs77395890	chr11:66335273-66335274	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
41	rs77098817	chr11:66335307-66335308	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
42	rs2242663	chr11:66335308-66335309	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance disease
43	rs553397943	chr11:66335346-66335347	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
44	rs573350477	chr11:66335354-66335355	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
45	rs542077488	chr11:66335373-66335374	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
46	rs139443555	chr11:66335384-66335385	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
47	rs531060614	chr11:66335385-66335386	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
48	rs143186834	chr11:66335389-66335390	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
49	rs117848405	chr11:66335390-66335391	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
50	rs191491162	chr11:66335399-66335400	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:93)

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
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
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	22522925	CNVD

Chromatin state (count:416 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:66319000-66337800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr11:66326600-66334800	Weak transcription	Colon Smooth Muscle	Colon
3	chr11:66326800-66334800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
4	chr11:66326800-66334800	Weak transcription	Pancreas	Pancrea
5	chr11:66326800-66335000	Weak transcription	Psoas Muscle	Psoas
6	chr11:66326800-66335000	Weak transcription	Rectal Mucosa Donor 29	rectum
7	chr11:66326800-66335200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr11:66326800-66335200	Weak transcription	Esophagus	oesophagus
9	chr11:66326800-66335200	Weak transcription	Left Ventricle	heart
10	chr11:66326800-66335200	Weak transcription	Rectal Smooth Muscle	rectum
11	chr11:66327000-66335200	Weak transcription	Fetal Heart	heart
12	chr11:66327200-66335000	Weak transcription	Primary T helper cells fromperipheralblood	blood
13	chr11:66327400-66335200	Weak transcription	Right Atrium	heart
14	chr11:66328000-66335000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
15	chr11:66328400-66334800	Strong transcription	Fetal Stomach	stomach
16	chr11:66329000-66335000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
17	chr11:66329400-66334800	Strong transcription	Brain Germinal Matrix	brain
18	chr11:66329400-66336600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
19	chr11:66330400-66334800	Strong transcription	Stomach Smooth Muscle	stomach
20	chr11:66330400-66335600	Weak transcription	HUES64 Cell Line	embryonic stem cell
21	chr11:66330400-66337800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
22	chr11:66330600-66336800	Weak transcription	HUES48 Cell Line	embryonic stem cell
23	chr11:66330800-66334800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
24	chr11:66330800-66335000	Weak transcription	Duodenum Mucosa	Duodenum
25	chr11:66330800-66336000	Weak transcription	Fetal Lung	lung
26	chr11:66331000-66335600	Weak transcription	Aorta	Aorta
27	chr11:66331200-66336600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
28	chr11:66331400-66335200	Weak transcription	Colonic Mucosa	Colon
29	chr11:66331400-66337800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
30	chr11:66331600-66337800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
31	chr11:66332000-66335600	Weak transcription	Pancreatic Islets	Pancreatic Islet
32	chr11:66332000-66336600	Weak transcription	H9 Cell Line	embryonic stem cell
33	chr11:66332200-66335400	Weak transcription	HUES6 Cell Line	embryonic stem cell
34	chr11:66332200-66335400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
35	chr11:66333000-66334800	Weak transcription	Fetal Muscle Leg	muscle
36	chr11:66333600-66335000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
37	chr11:66333600-66335200	Weak transcription	Liver	Liver
38	chr11:66333600-66335200	Weak transcription	Duodenum Smooth Muscle	Duodenum
39	chr11:66333600-66335600	Weak transcription	Placenta Amnion	Placenta Amnion
40	chr11:66333800-66334800	Weak transcription	Adipose Nuclei	Adipose
41	chr11:66333800-66334800	Weak transcription	Brain Substantia Nigra	brain
42	chr11:66333800-66334800	Weak transcription	Fetal Brain Female	brain
43	chr11:66333800-66334800	Weak transcription	Spleen	Spleen
44	chr11:66333800-66335200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
45	chr11:66333800-66335200	Weak transcription	Right Ventricle	heart
46	chr11:66334000-66334800	Weak transcription	Gastric	stomach
47	chr11:66334000-66335000	Weak transcription	Cortex derived primary cultured neurospheres	brain
48	chr11:66334000-66335200	Weak transcription	Lung	lung
49	chr11:66334200-66334800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
50	chr11:66334200-66334800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin

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