Variant report

Variant	esv3421132
Chromosome Location	chr11:67210476-67211924
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:355)
CpG islands
(count:855)
Chromatin interactive
region (count:20)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:355 , 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	chr11:67211283-67211477	HepG2	liver:	n/a	n/a
2	ARID3A	chr11:67211286-67211460	K562	blood:	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	chr11:67210851-67211463	HepG2	liver:	n/a	chr11:67211394-67211403 chr11:67211395-67211404 chr11:67211388-67211409
8	BHLHE40	chr11:67210920-67211546	GM12878	blood:	n/a	chr11:67211394-67211403 chr11:67211395-67211404 chr11:67211388-67211409
9	BHLHE40	chr11:67211020-67211412	A549	lung:	n/a	chr11:67211394-67211403 chr11:67211395-67211404 chr11:67211388-67211409
10	BHLHE40	chr11:67210910-67211550	K562	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	chr11:67210713-67211397	Hela-S3	cervix:	n/a	n/a
18	CHD2	chr11:67210596-67211366	GM12878	blood:	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	chr11:67211223-67211399	K562	blood:	n/a	n/a
22	CTCF	chr11:67211240-67211390	HBMEC	blood vessel:	n/a	n/a
23	CTCF	chr11:67211260-67211410	HPF	lung:	n/a	n/a
24	CTCF	chr11:67211180-67211330	GM06990	blood:	n/a	n/a
25	CTCF	chr11:67211100-67211250	GM12871	blood:	n/a	n/a
26	CTCF	chr11:67211340-67211490	GM12874	blood:	n/a	n/a
27	CTCF	chr11:67211200-67211350	GM12878	blood:	n/a	n/a
28	CTCF	chr11:67211280-67211430	HCPEpiC	choroid plexus:	n/a	n/a
29	CTCF	chr11:67211260-67211410	HCPEpiC	choroid plexus:	n/a	n/a
30	CTCF	chr11:67211280-67211430	MCF-7	breast:	n/a	n/a
31	CTCF	chr11:67211180-67211330	SK-N-SH_RA	brain:	n/a	n/a
32	CTCF	chr11:67211200-67211350	AG04449	skin:	n/a	n/a
33	CTCF	chr11:67211200-67211350	GM12873	blood:	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	chr11:67210539-67210795	K562	blood:	n/a	n/a
41	ELF1	chr11:67210836-67211236	SK-N-SH	brain:	n/a	n/a
42	ELF1	chr11:67210157-67211556	GM12878	blood:	n/a	n/a
43	ELF1	chr11:67210832-67211411	HCT-116	colon:	n/a	n/a
44	ELF1	chr11:67210564-67211380	K562	blood:	n/a	n/a
45	ELF1	chr11:67210768-67211094	A549	lung:	n/a	n/a
46	ELF1	chr11:67210816-67211266	MCF-7	breast:	n/a	n/a
47	ELF1	chr11:67210742-67211173	SK-N-SH	brain:	n/a	n/a
48	ELF1	chr11:67210810-67211263	HepG2	liver:	n/a	n/a
49	ELF1	chr11:67210666-67211430	MCF-7	breast:	n/a	n/a
50	ELF1	chr11:67209722-67211558	GM12878	blood:	n/a	n/a

(count:855 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:67211701-67211751	HL-60	blood:	n/a
2	chr11:67211701-67211751	HL-60	blood:	n/a
3	chr11:67211128-67211178	HCF	heart:	n/a
4	chr11:67211017-67211067	HepG2	liver:	n/a
5	chr11:67211379-67211429	NT2-D1	testis:	n/a
6	chr11:67211080-67211130	IMR90	lung:	fetal
7	chr11:67211318-67211368	HEK293	kidney:	embryo
8	chr11:67211054-67211104	NB4	blood:	n/a
9	chr11:67211308-67211358	HEK293	kidney:	embryo
10	chr11:67211245-67211295	HAEpiC	amniotic membrane:	n/a
11	chr11:67211318-67211368	CMK	blood:	n/a
12	chr11:67211379-67211429	HIPEpiC	eye:	n/a
13	chr11:67211717-67211767	HCM	heart:	n/a
14	chr11:67211701-67211751	AG09309	skin:	n/a
15	chr11:67211701-67211751	ECC-1	luminal epithelium:	n/a
16	chr11:67211308-67211358	GM06990	blood:	n/a
17	chr11:67211701-67211751	SKMC	muscle:	n/a
18	chr11:67211057-67211107	NT2-D1	testis:	n/a
19	chr11:67211128-67211178	AG04450	lung:	fetal
20	chr11:67211308-67211358	PrEC	prostate:	n/a
21	chr11:67211701-67211751	IMR90	lung:	fetal
22	chr11:67211128-67211178	HRPEpiC	eye:	n/a
23	chr11:67211300-67211350	AG09319	gingival:	n/a
24	chr11:67211245-67211295	AG04449	skin:	fetal
25	chr11:67211057-67211107	HEEpiC	esophagus:	n/a
26	chr11:67211080-67211130	AG10803	skin:	n/a
27	chr11:67211308-67211358	LNCaP	prostate:	n/a
28	chr11:67211701-67211751	GM19239	blood:	n/a
29	chr11:67211128-67211178	AG04449	skin:	fetal
30	chr11:67211245-67211295	SKMC	muscle:	n/a
31	chr11:67210812-67210862	Caco-2	colon:	n/a
32	chr11:67211318-67211368	PANC-1	pancreas:	n/a
33	chr11:67210812-67210862	HIPEpiC	eye:	n/a
34	chr11:67211318-67211368	NHDF-neo	bronchial:	n/a
35	chr11:67211080-67211130	MCF-7	breast:	n/a
36	chr11:67211128-67211178	HRE	kidney:	n/a
37	chr11:67211379-67211429	AG10803	skin:	n/a
38	chr11:67211057-67211107	GM12878	blood:	n/a
39	chr11:67211701-67211751	SAEC	small airway:	n/a
40	chr11:67211315-67211365	HL-60	blood:	n/a
41	chr11:67211245-67211295	BJ	skin:	n/a
42	chr11:67210812-67210862	ECC-1	luminal epithelium:	n/a
43	chr11:67210812-67210862	PANC-1	pancreas:	n/a
44	chr11:67211379-67211429	PrEC	prostate:	n/a
45	chr11:67211315-67211365	LNCaP	prostate:	n/a
46	chr11:67211128-67211178	SK-N-SH	brain:	n/a
47	chr11:67211717-67211767	HRCEpiC	kidney:	n/a
48	chr11:67211308-67211358	HUVEC	blood vessel:	n/a
49	chr11:67211245-67211295	GM06990	blood:	n/a
50	chr11:67211054-67211104	GM12891	blood:	n/a

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

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

No data

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

Extended variants
information (count: 43 )
Associated
traits (count: 94 )

Variant overlapped rSNPs/rCNVs (count:43 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	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
2	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
3	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
4	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
5	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
6	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
7	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
8	rs550916783	chr11:67210880-67210881	Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	21 gene(s)	Overlapped CNVs	n/a
9	rs569318034	chr11:67210915-67210916	Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	21 gene(s)	Overlapped CNVs	n/a
10	rs530591918	chr11:67210971-67210972	Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	21 gene(s)	Overlapped CNVs	n/a
11	rs547690682	chr11:67210983-67210984	Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	21 gene(s)	Overlapped CNVs	n/a
12	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
13	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
14	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
15	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
16	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
17	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
18	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
19	rs12799004	chr11:67211196-67211197	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
20	rs557359517	chr11:67211235-67211236	Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
21	rs373878138	chr11:67211250-67211251	Active TSS Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
22	rs575732515	chr11:67211265-67211266	Active TSS Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
23	rs536731224	chr11:67211302-67211303	Active TSS Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
24	rs377245548	chr11:67211380-67211381	Active TSS Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
25	rs554802405	chr11:67211498-67211499	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
26	rs185322615	chr11:67211501-67211502	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
27	rs540518667	chr11:67211516-67211517	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
28	rs1808279	chr11:67211569-67211570	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
29	rs577083102	chr11:67211573-67211574	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
30	rs373743205	chr11:67211622-67211623	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
31	rs544518431	chr11:67211623-67211624	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
32	rs562915154	chr11:67211638-67211639	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
33	rs530450738	chr11:67211702-67211703	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
34	rs562317749	chr11:67211707-67211708	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
35	rs549046947	chr11:67211721-67211722	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
36	rs141735426	chr11:67211725-67211726	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
37	rs71461649	chr11:67211778-67211779	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
38	rs532035056	chr11:67211779-67211780	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
39	rs528284014	chr11:67211794-67211795	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
40	rs34367256	chr11:67211795-67211796	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
41	rs529527657	chr11:67211816-67211817	Flanking Active TSS Enhancers Weak transcription Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
42	rs544911841	chr11:67211847-67211848	Flanking Active TSS Enhancers Weak transcription Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
43	rs189806540	chr11:67211859-67211860	Flanking Active TSS Enhancers Weak transcription Active TSS	TF binding region Chromatin interactive region	7 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:309 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:67205800-67211200	Enhancers	Primary B cells from cord blood	blood
2	chr11:67206800-67210600	Transcr. at gene 5' and 3'	Foreskin Melanocyte Primary Cells skin01	Skin
3	chr11:67207000-67211200	Enhancers	Primary B cells from peripheral blood	blood
4	chr11:67207000-67211200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
5	chr11:67207800-67211200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
6	chr11:67207800-67211200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
7	chr11:67208000-67210600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
8	chr11:67208000-67210800	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
9	chr11:67208000-67211000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
10	chr11:67208000-67211000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
11	chr11:67208000-67211200	Enhancers	Primary T cells fromperipheralblood	blood
12	chr11:67208200-67210600	Enhancers	Primary T helper naive cells from peripheral blood	blood
13	chr11:67208200-67211200	Enhancers	Primary T helper cells PMA-I stimulated	--
14	chr11:67208400-67211200	Enhancers	Primary T killer memory cells from peripheral blood	blood
15	chr11:67209400-67211000	Enhancers	Primary T regulatory cells fromperipheralblood	blood
16	chr11:67209600-67210600	Flanking Active TSS	Stomach Mucosa	stomach
17	chr11:67209600-67210600	Enhancers	Dnd41	blood
18	chr11:67209600-67211800	Active TSS	Rectal Smooth Muscle	rectum
19	chr11:67209800-67210600	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
20	chr11:67209800-67210600	Flanking Active TSS	Muscle Satellite Cultured Cells	--
21	chr11:67209800-67210600	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
22	chr11:67209800-67210600	Flanking Active TSS	Brain Cingulate Gyrus	brain
23	chr11:67209800-67210600	Flanking Active TSS	Colonic Mucosa	Colon
24	chr11:67209800-67210600	Transcr. at gene 5' and 3'	Fetal Intestine Small	intestine
25	chr11:67209800-67210600	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
26	chr11:67209800-67210600	Flanking Active TSS	NHEK	skin
27	chr11:67209800-67210800	Flanking Active TSS	Thymus	Thymus
28	chr11:67209800-67210800	Flanking Active TSS	NH-A	brain
29	chr11:67209800-67212000	Active TSS	HUES48 Cell Line	embryonic stem cell
30	chr11:67209800-67212200	Enhancers	Fetal Brain Male	brain
31	chr11:67210000-67210600	Enhancers	Primary T cells from cord blood	blood
32	chr11:67210000-67210600	Enhancers	Primary hematopoietic stem cells	blood
33	chr11:67210000-67210600	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
34	chr11:67210000-67210600	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
35	chr11:67210000-67210600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
36	chr11:67210000-67210600	Flanking Active TSS	Adipose Nuclei	Adipose
37	chr11:67210000-67210600	Flanking Active TSS	Liver	Liver
38	chr11:67210000-67210600	Flanking Active TSS	Brain Substantia Nigra	brain
39	chr11:67210000-67210600	Flanking Active TSS	Fetal Adrenal Gland	Adrenal Gland
40	chr11:67210000-67210600	Flanking Active TSS	Fetal Stomach	stomach
41	chr11:67210000-67210600	Flanking Active TSS	Lung	lung
42	chr11:67210000-67210600	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
43	chr11:67210000-67210600	Flanking Active TSS	HMEC	breast
44	chr11:67210000-67210800	Flanking Active TSS	Placenta	Placenta
45	chr11:67210000-67210800	Flanking Active TSS	Stomach Smooth Muscle	stomach
46	chr11:67210000-67210800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
47	chr11:67210000-67211600	Active TSS	Brain Angular Gyrus	brain
48	chr11:67210000-67211600	Active TSS	Pancreatic Islets	Pancreatic Islet
49	chr11:67210000-67211800	Active TSS	Small Intestine	intestine
50	chr11:67210000-67212000	Active TSS	HUES6 Cell Line	embryonic stem cell

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