Variant report

Variant	esv3324830
Chromosome Location	chr11:67209801-67212349
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:391)
CpG islands
(count:1160)
Chromatin interactive
region (count:20)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:391 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:67211286-67211460	K562	blood:	n/a	n/a
2	ARID3A	chr11:67211283-67211477	HepG2	liver:	n/a	n/a
3	ATF2	chr11:67210936-67211544	GM12878	blood:	n/a	n/a
4	BACH1	chr11:67211324-67211347	K562	blood:	n/a	n/a
5	BACH1	chr11:67211110-67211462	H1-hESC	embryonic stem cell:	n/a	n/a
6	BCL3	chr11:67210757-67211321	GM12878	blood:	n/a	n/a
7	BHLHE40	chr11:67210910-67211550	K562	blood:	n/a	chr11:67211394-67211403 chr11:67211395-67211404 chr11:67211388-67211409
8	BHLHE40	chr11:67211020-67211412	A549	lung:	n/a	chr11:67211394-67211403 chr11:67211395-67211404 chr11:67211388-67211409
9	BHLHE40	chr11:67210851-67211463	HepG2	liver:	n/a	chr11:67211394-67211403 chr11:67211395-67211404 chr11:67211388-67211409
10	BHLHE40	chr11:67210920-67211546	GM12878	blood:	n/a	chr11:67211394-67211403 chr11:67211395-67211404 chr11:67211388-67211409
11	CBX3	chr11:67211052-67211341	K562	blood:	n/a	n/a
12	CCNT2	chr11:67210942-67211349	K562	blood:	n/a	n/a
13	CEBPB	chr11:67211210-67211317	H1-hESC	embryonic stem cell:	n/a	n/a
14	CEBPB	chr11:67211178-67211301	Hela-S3	cervix:	n/a	n/a
15	CEBPD	chr11:67210971-67211329	HepG2	liver:	n/a	n/a
16	CHD1	chr11:67211120-67211556	GM12878	blood:	n/a	n/a
17	CHD2	chr11:67210596-67211366	GM12878	blood:	n/a	n/a
18	CHD2	chr11:67210713-67211397	Hela-S3	cervix:	n/a	n/a
19	CREB1	chr11:67210783-67211537	HepG2	liver:	n/a	n/a
20	CREB1	chr11:67211007-67211339	A549	lung:	n/a	n/a
21	CTCF	chr11:67211240-67211390	HBMEC	blood vessel:	n/a	n/a
22	CTCF	chr11:67211200-67211350	GM12878	blood:	n/a	n/a
23	CTCF	chr11:67211340-67211490	GM12874	blood:	n/a	n/a
24	CTCF	chr11:67211260-67211410	HPF	lung:	n/a	n/a
25	CTCF	chr11:67211280-67211430	HCPEpiC	choroid plexus:	n/a	n/a
26	CTCF	chr11:67211223-67211399	K562	blood:	n/a	n/a
27	CTCF	chr11:67211180-67211330	SK-N-SH_RA	brain:	n/a	n/a
28	CTCF	chr11:67211200-67211350	AG04449	skin:	n/a	n/a
29	CTCF	chr11:67211200-67211350	GM12873	blood:	n/a	n/a
30	CTCF	chr11:67211180-67211330	GM06990	blood:	n/a	n/a
31	CTCF	chr11:67211100-67211250	GM12871	blood:	n/a	n/a
32	CTCF	chr11:67211280-67211430	MCF-7	breast:	n/a	n/a
33	CTCF	chr11:67211260-67211410	HCPEpiC	choroid plexus:	n/a	n/a
34	E2F4	chr11:67211225-67211533	MCF10A-Er-Src	breast:	n/a	n/a
35	E2F6	chr11:67210922-67211396	K562	blood:	n/a	n/a
36	EGR1	chr11:67210825-67211255	GM12878	blood:	n/a	chr11:67210958-67210967 chr11:67211002-67211016
37	EGR1	chr11:67210781-67211408	K562	blood:	n/a	chr11:67210958-67210967 chr11:67211002-67211016
38	EGR1	chr11:67211079-67211393	GM12878	blood:	n/a	n/a
39	EGR1	chr11:67210816-67211408	K562	blood:	n/a	chr11:67210958-67210967 chr11:67211002-67211016
40	ELF1	chr11:67210810-67211263	HepG2	liver:	n/a	n/a
41	ELF1	chr11:67210832-67211411	HCT-116	colon:	n/a	n/a
42	ELF1	chr11:67210742-67211173	SK-N-SH	brain:	n/a	n/a
43	ELF1	chr11:67210564-67211380	K562	blood:	n/a	n/a
44	ELF1	chr11:67210836-67211236	SK-N-SH	brain:	n/a	n/a
45	ELF1	chr11:67210804-67211368	K562	blood:	n/a	n/a
46	ELF1	chr11:67210157-67211556	GM12878	blood:	n/a	n/a
47	ELF1	chr11:67210816-67211266	MCF-7	breast:	n/a	n/a
48	ELF1	chr11:67210745-67211396	HepG2	liver:	n/a	n/a
49	ELF1	chr11:67209722-67211558	GM12878	blood:	n/a	n/a
50	ELF1	chr11:67210539-67210795	K562	blood:	n/a	n/a

(count:1160 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:67211080-67211130	U87	brain:	n/a
2	chr11:67211080-67211130	U87	brain:	n/a
3	chr11:67210192-67210242	U87	brain:	n/a
4	chr11:67211701-67211751	LNCaP	prostate:	n/a
5	chr11:67210812-67210862	HCT-116	colon:	n/a
6	chr11:67211128-67211178	AoSMC	blood vessel:	n/a
7	chr11:67211300-67211350	NHDF-neo	bronchial:	n/a
8	chr11:67211701-67211751	H1-hESC	embryonic stem cell:	embryo
9	chr11:67211080-67211130	HEEpiC	esophagus:	n/a
10	chr11:67211318-67211368	SK-N-MC	brain:	n/a
11	chr11:67211379-67211429	ECC-1	luminal epithelium:	n/a
12	chr11:67211057-67211107	SK-N-SH_RA	brain:	n/a
13	chr11:67211245-67211295	HRPEpiC	eye:	n/a
14	chr11:67211080-67211130	RPTEC	kidney:	n/a
15	chr11:67211308-67211358	PFSK-1	brain:	n/a
16	chr11:67210033-67210083	HCPEpiC	choroid plexus:	n/a
17	chr11:67211054-67211104	PFSK-1	brain:	n/a
18	chr11:67210130-67210180	RPTEC	kidney:	n/a
19	chr11:67211379-67211429	T-47D	breast:	n/a
20	chr11:67210225-67210275	Hepatocyte	liver:	n/a
21	chr11:67211245-67211295	HCPEpiC	choroid plexus:	n/a
22	chr11:67211057-67211107	RPTEC	kidney:	n/a
23	chr11:67211057-67211107	SAEC	small airway:	n/a
24	chr11:67210812-67210862	HCPEpiC	choroid plexus:	n/a
25	chr11:67211128-67211178	HRE	kidney:	n/a
26	chr11:67211128-67211178	MCF-7	breast:	n/a
27	chr11:67210812-67210862	HCM	heart:	n/a
28	chr11:67211017-67211067	HEEpiC	esophagus:	n/a
29	chr11:67210033-67210083	U87	brain:	n/a
30	chr11:67210812-67210862	ovcar-3	ovarian:	n/a
31	chr11:67211308-67211358	U87	brain:	n/a
32	chr11:67211057-67211107	GM19239	blood:	n/a
33	chr11:67211017-67211067	ovcar-3	ovarian:	n/a
34	chr11:67211300-67211350	GM06990	blood:	n/a
35	chr11:67211057-67211107	HPAEpiC	pulmonary alveolar:	n/a
36	chr11:67211379-67211429	MCF10A-Er-Src	breast:	n/a
37	chr11:67211017-67211067	Hepatocyte	liver:	n/a
38	chr11:67211318-67211368	NHBE	bronchial:	n/a
39	chr11:67210192-67210242	HPAEpiC	pulmonary alveolar:	n/a
40	chr11:67211054-67211104	HCT-116	colon:	n/a
41	chr11:67211318-67211368	MCF10A-Er-Src	breast:	n/a
42	chr11:67211017-67211067	SK-N-SH	brain:	n/a
43	chr11:67211300-67211350	MCF10A-Er-Src	breast:	n/a
44	chr11:67211245-67211295	AG04449	skin:	fetal
45	chr11:67211057-67211107	HRE	kidney:	n/a
46	chr11:67211701-67211751	ovcar-3	ovarian:	n/a
47	chr11:67211017-67211067	GM12892	blood:	n/a
48	chr11:67211318-67211368	ECC-1	luminal epithelium:	n/a
49	chr11:67210033-67210083	AG09319	gingival:	n/a
50	chr11:67210225-67210275	AG09309	skin:	n/a

(count:20 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:67209787..67211313-chr11:67271082..67272865,2	MCF-7	breast:
2	chr11:67165362..67170814-chr11:67205782..67211749,9	K562	blood:
3	chr11:67124441..67126848-chr11:67209187..67211107,2	K562	blood:
4	chr11:67209395..67211059-chr11:67288619..67291060,2	K562	blood:
5	chr1:151319500..151320189-chr11:67210733..67211584,2	Hela-S3	cervix:
6	chr11:67207285..67211032-chr11:67270341..67273194,4	K562	blood:
7	chr11:67185549..67189385-chr11:67208691..67212904,6	K562	blood:
8	chr11:67206947..67211030-chr11:67273670..67277577,4	MCF-7	breast:
9	chr11:67140134..67141664-chr11:67209999..67212449,2	K562	blood:
10	chr11:67211079..67212845-chr11:67271889..67273813,2	MCF-7	breast:
11	chr11:67210395..67211138-chr3:156877805..156878549,2	Hela-S3	cervix:
12	chr11:67209798..67211457-chr20:55841438..55843138,2	MCF-7	breast:
13	chr11:67210580..67211479-chr15:81281844..81282702,2	Hela-S3	cervix:
14	chr11:67204954..67212426-chr11:67228820..67232211,6	K562	blood:
15	chr11:67210127..67211102-chr17:43298747..43299743,2	Hela-S3	cervix:
16	chr11:67208782..67211032-chr11:67270751..67273545,3	K562	blood:
17	chr11:67210748..67211271-chr11:67235396..67236381,2	Hela-S3	cervix:
18	chr11:67208958..67211217-chr17:56736613..56738121,2	MCF-7	breast:
19	chr11:67210699..67211404-chr3:139108261..139109180,2	Hela-S3	cervix:
20	chr11:67207904..67210724-chr11:67272140..67274356,2	MCF-7	breast:

No data

Variant related genes	Relation type
PTPRCAP	TF binding region
CORO1B	TF binding region
PTPRCAP	CpG island
CORO1B	CpG island
ENSG00000172508	chromatin interactions
ENSG00000172663	chromatin interactions
ENSG00000110697	chromatin interactions
ENSG00000143390	chromatin interactions
ENSG00000101144	chromatin interactions
ENSG00000167791	chromatin interactions
ENSG00000163660	chromatin interactions
ENSG00000270169	chromatin interactions
ENSG00000248932	chromatin interactions
ENSG00000256514	chromatin interactions
ENSG00000226308	chromatin interactions
ENSG00000175505	chromatin interactions
ENSG00000184432	chromatin interactions
ENSG00000175482	chromatin interactions
ENSG00000172531	chromatin interactions
ENSG00000167797	chromatin interactions
ENSG00000184922	chromatin interactions
ENSG00000267121	chromatin interactions
ENSG00000117899	chromatin interactions
ENSG00000202077	chromatin interactions

Extended variants
information (count: 94 )
Associated
traits (count: 94 )

Variant overlapped rSNPs/rCNVs (count:94 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs370889955	chr11:67209858-67209859	Weak transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Active TSS Enhancers Strong transcription	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
2	rs376683723	chr11:67209860-67209861	Weak transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Active TSS Enhancers Strong transcription	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
3	rs80182011	chr11:67209869-67209870	Weak transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Active TSS Enhancers Strong transcription	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
4	rs545494856	chr11:67209877-67209878	Weak transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Active TSS Enhancers Strong transcription	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
5	rs79903011	chr11:67209889-67209890	Weak transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Active TSS Enhancers Strong transcription	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
6	rs374014388	chr11:67209898-67209899	Weak transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Active TSS Enhancers Strong transcription	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
7	rs145922150	chr11:67209903-67209904	Weak transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Active TSS Enhancers Strong transcription	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
8	rs138962974	chr11:67209919-67209920	Weak transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Active TSS Enhancers Strong transcription	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
9	rs561335766	chr11:67209953-67209954	Weak transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Active TSS Enhancers Strong transcription	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
10	rs200603268	chr11:67209977-67209978	Weak transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Active TSS Enhancers Strong transcription	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
11	rs547002578	chr11:67210012-67210013	Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Active TSS Genic enhancers	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
12	rs76972551	chr11:67210015-67210016	Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Active TSS Genic enhancers	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
13	rs532800018	chr11:67210030-67210031	Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Active TSS Genic enhancers	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
14	rs141337120	chr11:67210033-67210034	Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
15	rs201718860	chr11:67210044-67210045	Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
16	rs569460830	chr11:67210060-67210061	Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
17	rs150308810	chr11:67210079-67210080	Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
18	rs367836155	chr11:67210107-67210108	Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Active TSS Genic enhancers	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
19	rs373980652	chr11:67210155-67210156	Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
20	rs138355876	chr11:67210163-67210164	Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
21	rs555497234	chr11:67210176-67210177	Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
22	rs567364140	chr11:67210225-67210226	Active TSS Flanking Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
23	rs534889296	chr11:67210277-67210278	Active TSS Flanking Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
24	rs35024070	chr11:67210282-67210283	Active TSS Flanking Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
25	rs34212205	chr11:67210315-67210316	Active TSS Flanking Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	16 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs35904314	chr11:67210323-67210324	Active TSS Flanking Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
27	rs114586197	chr11:67210330-67210331	Active TSS Flanking Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
28	rs546247620	chr11:67210384-67210385	Active TSS Flanking Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
29	rs189513044	chr11:67210404-67210405	Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
30	rs557485761	chr11:67210406-67210407	Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
31	rs116519373	chr11:67210430-67210431	Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
32	rs115427403	chr11:67210441-67210442	Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
33	rs561507219	chr11:67210503-67210504	Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
34	rs528710609	chr11:67210540-67210541	Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
35	rs540906593	chr11:67210601-67210602	Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
36	rs193086132	chr11:67210729-67210730	Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
37	rs532763815	chr11:67210738-67210739	Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	20 gene(s)	Overlapped CNVs	n/a
38	rs375611930	chr11:67210787-67210788	Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	21 gene(s)	Overlapped CNVs	n/a
39	rs562540870	chr11:67210792-67210793	Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	21 gene(s)	Overlapped CNVs	n/a
40	rs550916783	chr11:67210880-67210881	Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	21 gene(s)	Overlapped CNVs	n/a
41	rs569318034	chr11:67210915-67210916	Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	21 gene(s)	Overlapped CNVs	n/a
42	rs530591918	chr11:67210971-67210972	Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	21 gene(s)	Overlapped CNVs	n/a
43	rs547690682	chr11:67210983-67210984	Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	21 gene(s)	Overlapped CNVs	n/a
44	rs548826676	chr11:67211012-67211013	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	21 gene(s)	Overlapped CNVs	n/a
45	rs567432387	chr11:67211103-67211104	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
46	rs370173002	chr11:67211111-67211112	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
47	rs546860950	chr11:67211140-67211141	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
48	rs571612879	chr11:67211149-67211150	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
49	rs538935453	chr11:67211190-67211191	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
50	rs12798511	chr11:67211195-67211196	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:94)

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
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
Myelofibrosis	22110671	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	21364760	CNVD
Acute myeloid leukemia	21251322	CNVD
Lung cancer	19153074	CNVD
lymphocytic leukemia	21291569	CNVD
Colorectal cancer	22860045	CNVD
Hirschsprung''s Disease	21712996	CNVD
Schizophrenia	21399695	CNVD
Ovarian clear cell carcinoma	19293255	CNVD

Chromatin state (count:481 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:67196800-67210200	Weak transcription	Fetal Kidney	kidney
2	chr11:67197200-67210000	Strong transcription	Fetal Brain Female	brain
3	chr11:67197200-67210000	Weak transcription	Pancreatic Islets	Pancreatic Islet
4	chr11:67201600-67210000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
5	chr11:67202200-67210200	Genic enhancers	Breast Myoepithelial Primary Cells	Breast
6	chr11:67202400-67210200	Weak transcription	Psoas Muscle	Psoas
7	chr11:67203200-67210000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr11:67203200-67210400	Weak transcription	Ovary	ovary
9	chr11:67203800-67210400	Weak transcription	Aorta	Aorta
10	chr11:67205600-67210000	Weak transcription	Brain Angular Gyrus	brain
11	chr11:67205600-67210200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
12	chr11:67205600-67210400	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin01	Skin
13	chr11:67205800-67211200	Enhancers	Primary B cells from cord blood	blood
14	chr11:67206200-67210200	Genic enhancers	Fetal Muscle Trunk	muscle
15	chr11:67206200-67210200	Genic enhancers	Spleen	Spleen
16	chr11:67206800-67210200	Genic enhancers	Fetal Thymus	thymus
17	chr11:67206800-67210400	Weak transcription	Primary neutrophils fromperipheralblood	blood
18	chr11:67206800-67210600	Transcr. at gene 5' and 3'	Foreskin Melanocyte Primary Cells skin01	Skin
19	chr11:67207000-67210000	Enhancers	Liver	Liver
20	chr11:67207000-67210000	Genic enhancers	Pancreas	Pancrea
21	chr11:67207000-67211200	Enhancers	Primary B cells from peripheral blood	blood
22	chr11:67207000-67211200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
23	chr11:67207200-67210000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
24	chr11:67207200-67210000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
25	chr11:67207200-67210000	Weak transcription	Right Atrium	heart
26	chr11:67207200-67210400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
27	chr11:67207600-67210000	Weak transcription	Primary hematopoietic stem cells	blood
28	chr11:67207600-67210200	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin02	Skin
29	chr11:67207800-67210000	Genic enhancers	Lung	lung
30	chr11:67207800-67211200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
31	chr11:67207800-67211200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
32	chr11:67208000-67210600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
33	chr11:67208000-67210800	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
34	chr11:67208000-67211000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
35	chr11:67208000-67211000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
36	chr11:67208000-67211200	Enhancers	Primary T cells fromperipheralblood	blood
37	chr11:67208200-67210600	Enhancers	Primary T helper naive cells from peripheral blood	blood
38	chr11:67208200-67211200	Enhancers	Primary T helper cells PMA-I stimulated	--
39	chr11:67208400-67210400	Enhancers	Primary T helper cells fromperipheralblood	blood
40	chr11:67208400-67211200	Enhancers	Primary T killer memory cells from peripheral blood	blood
41	chr11:67208600-67210000	Genic enhancers	Brain Inferior Temporal Lobe	brain
42	chr11:67208800-67210000	Weak transcription	Placenta Amnion	Placenta Amnion
43	chr11:67209000-67210000	Weak transcription	Primary T cells from cord blood	blood
44	chr11:67209200-67210000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
45	chr11:67209200-67210000	Genic enhancers	Primary mononuclear cells fromperipheralblood	Blood
46	chr11:67209200-67210000	Weak transcription	Brain Germinal Matrix	brain
47	chr11:67209400-67210000	Genic enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
48	chr11:67209400-67210000	Transcr. at gene 5' and 3'	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr11:67209400-67210000	Enhancers	HUVEC	blood vessel
50	chr11:67209400-67210200	Transcr. at gene 5' and 3'	IMR90 fetal lung fibroblasts Cell Line	lung

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