Variant report

Variant	nsv1067893
Chromosome Location	chr11:67253452-67255013
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:194)
CpG islands
(count:62)
Chromatin interactive
region (count:13)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:194 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr11:67253870-67254812	GM12878	blood:	n/a	n/a
2	ATF2	chr11:67253764-67254694	GM12878	blood:	n/a	n/a
3	BATF	chr11:67254025-67254438	GM12878	blood:	n/a	n/a
4	BATF	chr11:67253866-67254740	GM12878	blood:	n/a	n/a
5	BCL11A	chr11:67254092-67254489	GM12878	blood:	n/a	chr11:67254371-67254380
6	BCL11A	chr11:67254004-67254731	GM12878	blood:	n/a	chr11:67254371-67254380
7	BCL3	chr11:67254063-67254687	GM12878	blood:	n/a	chr11:67254371-67254380
8	BCL3	chr11:67253970-67254657	GM12878	blood:	n/a	chr11:67254371-67254380
9	BCLAF1	chr11:67253735-67254791	GM12878	blood:	n/a	chr11:67254371-67254380
10	BCLAF1	chr11:67253881-67254716	GM12878	blood:	n/a	chr11:67254371-67254380
11	BHLHE40	chr11:67253390-67254649	GM12878	blood:	n/a	n/a
12	BHLHE40	chr11:67253524-67253529	K562	blood:	n/a	n/a
13	BRCA1	chr11:67254158-67254254	GM12878	blood:	n/a	n/a
14	CEBPB	chr11:67253406-67254840	GM12878	blood:	n/a	n/a
15	CEBPB	chr11:67254044-67254457	GM12878	blood:	n/a	n/a
16	CHD1	chr11:67254087-67254628	GM12878	blood:	n/a	n/a
17	CHD1	chr11:67253362-67253689	GM12878	blood:	n/a	n/a
18	CHD2	chr11:67253492-67254616	GM12878	blood:	n/a	n/a
19	CTCF	chr11:67253473-67253601	GM19239	blood:	n/a	n/a
20	CTCF	chr11:67253497-67253556	GM12891	blood:	n/a	n/a
21	CTCF	chr11:67254180-67254330	GM12873	blood:	n/a	n/a
22	CTCF	chr11:67253691-67253748	GM20000	blood:	n/a	n/a
23	CUX1	chr11:67253648-67254529	GM12878	blood:	n/a	n/a
24	EBF1	chr11:67253357-67253642	GM12878	blood:	n/a	n/a
25	EBF1	chr11:67253356-67254733	GM12878	blood:	n/a	chr11:67254366-67254375 chr11:67254364-67254377
26	EBF1	chr11:67253972-67254598	GM12878	blood:	n/a	chr11:67254366-67254375 chr11:67254364-67254377
27	EBF1	chr11:67253332-67254783	GM12878	blood:	n/a	chr11:67254366-67254375 chr11:67254364-67254377
28	EGR1	chr11:67254140-67254472	GM12878	blood:	n/a	chr11:67254326-67254340 chr11:67254398-67254408
29	EGR1	chr11:67254127-67254510	GM12878	blood:	n/a	chr11:67254326-67254340 chr11:67254398-67254408
30	ELF1	chr11:67253327-67253625	K562	blood:	n/a	n/a
31	ELF1	chr11:67253362-67253815	GM12878	blood:	n/a	n/a
32	ELF1	chr11:67253444-67254623	GM12878	blood:	n/a	n/a
33	ELF1	chr11:67254008-67254755	GM12878	blood:	n/a	n/a
34	ELK1	chr11:67254059-67254436	GM12878	blood:	n/a	n/a
35	EP300	chr11:67253645-67253765	GM12878	blood:	n/a	n/a
36	EP300	chr11:67254053-67254666	GM12878	blood:	n/a	n/a
37	EP300	chr11:67253587-67254591	GM12878	blood:	n/a	n/a
38	EP300	chr11:67253516-67254752	GM12878	blood:	n/a	n/a
39	EP300	chr11:67254046-67254578	GM12878	blood:	n/a	n/a
40	FOXM1	chr11:67254991-67255582	GM12878	blood:	n/a	n/a
41	FOXM1	chr11:67253768-67254764	GM12878	blood:	n/a	n/a
42	FOXM1	chr11:67253860-67254768	GM12878	blood:	n/a	n/a
43	FOXM1	chr11:67253380-67253834	GM12878	blood:	n/a	n/a
44	GTF2F1	chr11:67254368-67254409	K562	blood:	n/a	n/a
45	IRF3	chr11:67253471-67253475	GM12878	blood:	n/a	n/a
46	IRF4	chr11:67253941-67254810	GM12878	blood:	n/a	n/a
47	IRF4	chr11:67253927-67254730	GM12878	blood:	n/a	n/a
48	MAX	chr11:67253794-67254133	K562	blood:	n/a	n/a
49	MAX	chr11:67253353-67253696	K562	blood:	n/a	n/a
50	MAX	chr11:67253743-67254256	K562	blood:	n/a	n/a

(count:62 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:67254381-67254431	NH-A	brain:	n/a
2	chr11:67254381-67254431	NH-A	brain:	n/a
3	chr11:67254381-67254431	PrEC	prostate:	n/a
4	chr11:67254381-67254431	AG04450	lung:	fetal
5	chr11:67254381-67254431	SAEC	small airway:	n/a
6	chr11:67254381-67254431	HEEpiC	esophagus:	n/a
7	chr11:67254381-67254431	HCPEpiC	choroid plexus:	n/a
8	chr11:67254381-67254431	ECC-1	luminal epithelium:	n/a
9	chr11:67254381-67254431	ovcar-3	ovarian:	n/a
10	chr11:67254381-67254431	HPAEpiC	pulmonary alveolar:	n/a
11	chr11:67254381-67254431	Jurkat	blood:	n/a
12	chr11:67254381-67254431	HNPCEpiC	eye:	n/a
13	chr11:67254381-67254431	IMR90	lung:	fetal
14	chr11:67254381-67254431	HepG2	liver:	n/a
15	chr11:67254381-67254431	BE2_C	brain:	n/a
16	chr11:67254381-67254431	SK-N-MC	brain:	n/a
17	chr11:67254381-67254431	HMEC	breast:	n/a
18	chr11:67254381-67254431	GM06990	blood:	n/a
19	chr11:67254381-67254431	LNCaP	prostate:	n/a
20	chr11:67254381-67254431	AG09319	gingival:	n/a
21	chr11:67254381-67254431	PFSK-1	brain:	n/a
22	chr11:67254381-67254431	HRCEpiC	kidney:	n/a
23	chr11:67254381-67254431	HL-60	blood:	n/a
24	chr11:67254381-67254431	Hela-S3	cervix:	n/a
25	chr11:67254381-67254431	HAEpiC	amniotic membrane:	n/a
26	chr11:67254381-67254431	U87	brain:	n/a
27	chr11:67254381-67254431	PANC-1	pancreas:	n/a
28	chr11:67254381-67254431	AG04449	skin:	fetal
29	chr11:67254381-67254431	NHBE	bronchial:	n/a
30	chr11:67254381-67254431	SKMC	muscle:	n/a
31	chr11:67254381-67254431	AG10803	skin:	n/a
32	chr11:67254381-67254431	T-47D	breast:	n/a
33	chr11:67254381-67254431	HCF	heart:	n/a
34	chr11:67254381-67254431	GM12892	blood:	n/a
35	chr11:67254381-67254431	HEK293	kidney:	embryo
36	chr11:67254381-67254431	ProgFib	skin:	n/a
37	chr11:67254381-67254431	NB4	blood:	n/a
38	chr11:67254381-67254431	GM12891	blood:	n/a
39	chr11:67254381-67254431	NT2-D1	testis:	n/a
40	chr11:67254381-67254431	SK-N-SH	brain:	n/a
41	chr11:67254381-67254431	H1-hESC	embryonic stem cell:	embryo
42	chr11:67254381-67254431	HUVEC	blood vessel:	n/a
43	chr11:67254381-67254431	K562	blood:	n/a
44	chr11:67254381-67254431	Caco-2	colon:	n/a
45	chr11:67254381-67254431	CMK	blood:	n/a
46	chr11:67254381-67254431	GM19239	blood:	n/a
47	chr11:67254381-67254431	GM12878	blood:	n/a
48	chr11:67254381-67254431	SK-N-SH_RA	brain:	n/a
49	chr11:67254381-67254431	MCF10A-Er-Src	breast:	n/a
50	chr11:67254381-67254431	MCF-7	breast:	n/a

(count:13 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:67250038..67251911-chr11:67252963..67255145,2	MCF-7	breast:
2	chr11:67253095..67255847-chr16:2577337..2579833,2	MCF-7	breast:
3	chr11:67249454..67253550-chr11:67271231..67274487,6	MCF-7	breast:
4	chr11:67176577..67178931-chr11:67250966..67253943,2	MCF-7	breast:
5	chr11:67204772..67206775-chr11:67251398..67253520,2	K562	blood:
6	chr11:67249912..67253635-chr11:67270546..67273534,5	K562	blood:
7	chr11:67250658..67253558-chr11:67351233..67353250,2	K562	blood:
8	chr11:67252342..67255361-chr11:67262827..67265750,4	MCF-7	breast:
9	chr11:67252207..67254745-chr11:67287630..67289973,2	K562	blood:
10	chr11:67138872..67142169-chr11:67249496..67254071,4	MCF-7	breast:
11	chr11:67250656..67253599-chr11:67256113..67260551,5	K562	blood:
12	chr11:67207077..67209536-chr11:67252899..67255473,2	K562	blood:
13	chr11:67204772..67206774-chr11:67250564..67253520,2	K562	blood:

No data

Variant related genes	Relation type
AIP	TF binding region
AIP	CpG island
ENSG00000110711	chromatin interactions
ENSG00000256514	chromatin interactions
ENSG00000110697	chromatin interactions
ENSG00000162066	chromatin interactions
ENSG00000172725	chromatin interactions
ENSG00000175505	chromatin interactions
ENSG00000084207	chromatin interactions
ENSG00000213402	chromatin interactions

Extended variants
information (count: 68 )
Associated
traits (count: 96 )

Variant overlapped rSNPs/rCNVs (count:68 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs529876561	chr11:67253462-67253463	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers Active TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
2	rs541604795	chr11:67253552-67253553	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
3	rs560420345	chr11:67253553-67253554	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
4	rs7110021	chr11:67253564-67253565	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers Active TSS	TF binding region Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
5	rs552551578	chr11:67253606-67253607	Enhancers Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Strong transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
6	rs570710707	chr11:67253621-67253622	Enhancers Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Strong transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
7	rs144079780	chr11:67253637-67253638	Enhancers Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Strong transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
8	rs537961923	chr11:67253670-67253671	Enhancers Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Strong transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
9	rs630172	chr11:67253673-67253674	Enhancers Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Strong transcription	TF binding region Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
10	rs568550395	chr11:67253738-67253739	Enhancers Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Strong transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
11	rs114324917	chr11:67253807-67253808	Weak transcription Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
12	rs554043909	chr11:67253872-67253873	Weak transcription Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
13	rs566377437	chr11:67253889-67253890	Weak transcription Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
14	rs539702734	chr11:67253891-67253892	Weak transcription Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
15	rs76605055	chr11:67253919-67253920	Weak transcription Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
16	rs75081450	chr11:67253921-67253922	Weak transcription Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
17	rs146033798	chr11:67253927-67253928	Weak transcription Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
18	rs545231683	chr11:67253998-67253999	Weak transcription Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
19	rs183782643	chr11:67254028-67254029	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
20	rs543793232	chr11:67254030-67254031	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
21	rs555870918	chr11:67254143-67254144	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
22	rs575882653	chr11:67254256-67254257	Weak transcription Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
23	rs560187597	chr11:67254268-67254269	Weak transcription Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
24	rs574168393	chr11:67254283-67254284	Weak transcription Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
25	rs542025234	chr11:67254302-67254303	Weak transcription Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
26	rs560051165	chr11:67254329-67254330	Weak transcription Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
27	rs527588806	chr11:67254339-67254340	Weak transcription Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
28	rs188172321	chr11:67254350-67254351	Weak transcription Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
29	rs564397694	chr11:67254370-67254371	Weak transcription Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
30	rs572310439	chr11:67254371-67254372	Weak transcription Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
31	rs542612039	chr11:67254397-67254398	Weak transcription Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
32	rs200750110	chr11:67254405-67254406	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
33	rs377538917	chr11:67254434-67254435	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
34	rs202156895	chr11:67254459-67254460	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
35	rs547976657	chr11:67254460-67254461	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
36	rs200754493	chr11:67254461-67254462	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
37	rs371268619	chr11:67254470-67254471	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
38	rs539027647	chr11:67254471-67254472	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
39	rs376797001	chr11:67254481-67254482	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
40	rs551824427	chr11:67254482-67254483	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
41	rs531663925	chr11:67254489-67254490	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
42	rs139947406	chr11:67254493-67254494	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
43	rs142044984	chr11:67254496-67254497	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
44	rs11822907	chr11:67254509-67254510	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs574205552	chr11:67254510-67254511	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
46	rs181969066	chr11:67254512-67254513	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
47	rs267606537	chr11:67254515-67254516	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
48	rs1063385	chr11:67254522-67254523	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
49	rs201359503	chr11:67254530-67254531	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
50	rs267606538	chr11:67254543-67254544	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:96)

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
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
small cell lung cancer	20016488	CNVD
early-passage human iPS cells	21368824	CNVD
Pituitary adenoma	20530095	CNVD

Chromatin state (count:266 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:67250800-67254800	Weak transcription	Ovary	ovary
2	chr11:67251000-67253800	Enhancers	Primary hematopoietic stem cells	blood
3	chr11:67251000-67253800	Enhancers	Lung	lung
4	chr11:67251000-67254400	Enhancers	Spleen	Spleen
5	chr11:67251000-67257000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr11:67251000-67271000	Weak transcription	Pancreatic Islets	Pancreatic Islet
7	chr11:67251200-67257400	Weak transcription	H9 Cell Line	embryonic stem cell
8	chr11:67251200-67257400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
9	chr11:67251400-67253600	Weak transcription	Small Intestine	intestine
10	chr11:67251400-67255000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
11	chr11:67251400-67257000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr11:67251400-67268000	Weak transcription	HSMMtube	muscle
13	chr11:67251400-67271200	Weak transcription	HSMM	muscle
14	chr11:67251400-67271400	Weak transcription	HUVEC	blood vessel
15	chr11:67251600-67253600	Enhancers	Adipose Nuclei	Adipose
16	chr11:67251600-67253800	Enhancers	Breast Myoepithelial Primary Cells	Breast
17	chr11:67251600-67254000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr11:67251600-67254000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
19	chr11:67251600-67255200	Weak transcription	Osteobl	bone
20	chr11:67251600-67256400	Weak transcription	HMEC	breast
21	chr11:67251600-67256600	Weak transcription	HUES6 Cell Line	embryonic stem cell
22	chr11:67251600-67256600	Weak transcription	Aorta	Aorta
23	chr11:67251600-67256800	Weak transcription	HUES48 Cell Line	embryonic stem cell
24	chr11:67251600-67257200	Weak transcription	A549	lung
25	chr11:67251600-67259800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr11:67251600-67268400	Weak transcription	NH-A	brain
27	chr11:67251600-67268600	Strong transcription	Fetal Intestine Small	intestine
28	chr11:67251600-67270600	Weak transcription	Fetal Heart	heart
29	chr11:67251600-67271400	Weak transcription	NHDF-Ad	bronchial
30	chr11:67251800-67253600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
31	chr11:67251800-67253800	Enhancers	Hela-S3	cervix
32	chr11:67251800-67255400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
33	chr11:67252000-67254400	Enhancers	K562	blood
34	chr11:67252000-67255000	Weak transcription	Placenta Amnion	Placenta Amnion
35	chr11:67252000-67257600	Weak transcription	H1 Cell Line	embryonic stem cell
36	chr11:67252200-67253600	Weak transcription	Stomach Mucosa	stomach
37	chr11:67252200-67254000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
38	chr11:67252200-67254400	Weak transcription	Fetal Brain Female	brain
39	chr11:67252400-67254000	Weak transcription	Fetal Intestine Large	intestine
40	chr11:67252400-67254400	Weak transcription	Brain Substantia Nigra	brain
41	chr11:67252400-67254400	Weak transcription	Right Ventricle	heart
42	chr11:67252400-67255200	Weak transcription	Fetal Kidney	kidney
43	chr11:67252400-67256800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
44	chr11:67252400-67256800	Weak transcription	Muscle Satellite Cultured Cells	--
45	chr11:67252600-67253600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
46	chr11:67252600-67253600	Enhancers	Primary hematopoietic stem cells short term culture	blood
47	chr11:67252600-67253600	Weak transcription	Rectal Mucosa Donor 31	rectum
48	chr11:67252600-67253800	Weak transcription	Gastric	stomach
49	chr11:67252600-67254000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
50	chr11:67252600-67254000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin

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