Variant report

Variant	nsv983054
Chromosome Location	chr11:93467678-93468968
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:124)
CpG islands
(count:122)
Chromatin interactive
region (count:4)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:124 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr11:93467822-93468329	H1-hESC	embryonic stem cell:	n/a	n/a
2	CHD1	chr11:93467593-93467888	H1-hESC	embryonic stem cell:	n/a	n/a
3	CHD1	chr11:93468344-93468378	H1-hESC	embryonic stem cell:	n/a	n/a
4	CHD1	chr11:93468927-93469250	H1-hESC	embryonic stem cell:	n/a	n/a
5	E2F4	chr11:93468831-93468844	MCF10A-Er-Src	breast:	n/a	n/a
6	HEY1	chr11:93468562-93468901	K562	blood:	n/a	n/a
7	HEY1	chr11:93467637-93468637	HepG2	liver:	n/a	n/a
8	HEY1	chr11:93467826-93468336	K562	blood:	n/a	n/a
9	HEY1	chr11:93468714-93468960	HepG2	liver:	n/a	n/a
10	HEY1	chr11:93467611-93468533	HepG2	liver:	n/a	n/a
11	HEY1	chr11:93467882-93468715	K562	blood:	n/a	n/a
12	IRF1	chr11:93467602-93467831	K562	blood:	n/a	chr11:93467710-93467723 chr11:93467606-93467619 chr11:93467717-93467724
13	JUN	chr11:93468808-93469036	K562	blood:	n/a	n/a
14	JUND	chr11:93467931-93468090	H1-hESC	embryonic stem cell:	n/a	n/a
15	MBD4	chr11:93467783-93468426	HepG2	liver:	n/a	n/a
16	NFATC1	chr11:93467798-93468383	GM12878	blood:	n/a	n/a
17	PML	chr11:93467685-93468675	K562	blood:	n/a	n/a
18	PML	chr11:93467654-93469106	K562	blood:	n/a	n/a
19	PML	chr11:93467788-93468588	GM12878	blood:	n/a	n/a
20	POLR2A	chr11:93467957-93468085	HepG2	liver:	n/a	n/a
21	POLR2A	chr11:93467776-93468306	U87	brain:	n/a	n/a
22	POLR2A	chr11:93467515-93468442	U87	brain:	n/a	n/a
23	POLR2A	chr11:93465505-93475492	MCF10A-Er-Src	breast:	n/a	n/a
24	POLR2A	chr11:93468146-93468211	A549	lung:	n/a	n/a
25	POLR2A	chr11:93460023-93475421	GM12878	blood:	n/a	n/a
26	POLR2A	chr11:93466956-93468533	HepG2	liver:	n/a	n/a
27	POLR2A	chr11:93467520-93468938	GM12891	blood:	n/a	n/a
28	POLR2A	chr11:93467859-93468291	GM12878	blood:	n/a	n/a
29	POLR2A	chr11:93466348-93469559	PANC-1	pancreas:	n/a	n/a
30	POLR2A	chr11:93460849-93475367	GM18505	blood:	n/a	n/a
31	POLR2A	chr11:93467543-93468996	H1-hESC	embryonic stem cell:	n/a	n/a
32	POLR2A	chr11:93467573-93469496	HepG2	liver:	n/a	n/a
33	POLR2A	chr11:93467477-93468791	GM12891	blood:	n/a	n/a
34	POLR2A	chr11:93467892-93468096	A549	lung:	n/a	n/a
35	POLR2A	chr11:93467415-93469097	Hela-S3	cervix:	n/a	n/a
36	POLR2A	chr11:93467964-93468016	GM12878	blood:	n/a	n/a
37	POLR2A	chr11:93467787-93468856	HCT-116	colon:	n/a	n/a
38	POLR2A	chr11:93467641-93469099	GM12878	blood:	n/a	n/a
39	POLR2A	chr11:93467797-93468248	SK-N-MC	brain:	n/a	n/a
40	POLR2A	chr11:93467935-93468072	A549	lung:	n/a	n/a
41	POLR2A	chr11:93467664-93468953	K562	blood:	n/a	n/a
42	POLR2A	chr11:93467957-93468058	A549	lung:	n/a	n/a
43	POLR2A	chr11:93467263-93469529	HUVEC	blood vessel:	n/a	n/a
44	POLR2A	chr11:93467918-93468342	ECC-1	luminal epithelium:	n/a	n/a
45	POLR2A	chr11:93467487-93468789	Hela-S3	cervix:	n/a	n/a
46	POLR2A	chr11:93467469-93468957	H1-hESC	embryonic stem cell:	n/a	n/a
47	POLR2A	chr11:93460755-93469030	Hela-S3	cervix:	n/a	n/a
48	POLR2A	chr11:93467801-93468273	SK-N-SH	brain:	n/a	n/a
49	POLR2A	chr11:93466318-93469501	K562	blood:	n/a	n/a
50	POLR2A	chr11:93467829-93468634	ProgFib	skin:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:93468442-93468492	A549	lung:	n/a
2	chr11:93468466-93468516	HL-60	blood:	n/a
3	chr11:93468442-93468492	GM19239	blood:	n/a
4	chr11:93468466-93468516	AG04450	lung:	fetal
5	chr11:93468442-93468492	HEEpiC	esophagus:	n/a
6	chr11:93468442-93468492	HepG2	liver:	n/a
7	chr11:93468442-93468492	HCM	heart:	n/a
8	chr11:93468442-93468492	SK-N-MC	brain:	n/a
9	chr11:93468466-93468516	HUVEC	blood vessel:	n/a
10	chr11:93468466-93468516	BE2_C	brain:	n/a
11	chr11:93468442-93468492	T-47D	breast:	n/a
12	chr11:93468442-93468492	NH-A	brain:	n/a
13	chr11:93468442-93468492	HCF	heart:	n/a
14	chr11:93468442-93468492	PFSK-1	brain:	n/a
15	chr11:93468466-93468516	SKMC	muscle:	n/a
16	chr11:93468466-93468516	Caco-2	colon:	n/a
17	chr11:93468466-93468516	GM12892	blood:	n/a
18	chr11:93468442-93468492	AoSMC	blood vessel:	n/a
19	chr11:93468466-93468516	SK-N-SH_RA	brain:	n/a
20	chr11:93468442-93468492	K562	blood:	n/a
21	chr11:93468442-93468492	GM12892	blood:	n/a
22	chr11:93468466-93468516	BJ	skin:	n/a
23	chr11:93468466-93468516	MCF-7	breast:	n/a
24	chr11:93468466-93468516	HEEpiC	esophagus:	n/a
25	chr11:93468466-93468516	SK-N-SH	brain:	n/a
26	chr11:93468466-93468516	RPTEC	kidney:	n/a
27	chr11:93468442-93468492	AG10803	skin:	n/a
28	chr11:93468466-93468516	HIPEpiC	eye:	n/a
29	chr11:93468466-93468516	ECC-1	luminal epithelium:	n/a
30	chr11:93468466-93468516	GM19239	blood:	n/a
31	chr11:93468442-93468492	NHDF-neo	bronchial:	n/a
32	chr11:93468466-93468516	H1-hESC	embryonic stem cell:	embryo
33	chr11:93468466-93468516	SAEC	small airway:	n/a
34	chr11:93468466-93468516	PFSK-1	brain:	n/a
35	chr11:93468466-93468516	AG04449	skin:	fetal
36	chr11:93468442-93468492	PANC-1	pancreas:	n/a
37	chr11:93468442-93468492	GM06990	blood:	n/a
38	chr11:93468442-93468492	MCF10A-Er-Src	breast:	n/a
39	chr11:93468442-93468492	Jurkat	blood:	n/a
40	chr11:93468466-93468516	HCPEpiC	choroid plexus:	n/a
41	chr11:93468466-93468516	Hela-S3	cervix:	n/a
42	chr11:93468442-93468492	ovcar-3	ovarian:	n/a
43	chr11:93468442-93468492	U87	brain:	n/a
44	chr11:93468442-93468492	HRPEpiC	eye:	n/a
45	chr11:93468442-93468492	ProgFib	skin:	n/a
46	chr11:93468442-93468492	SAEC	small airway:	n/a
47	chr11:93468442-93468492	NHBE	bronchial:	n/a
48	chr11:93468442-93468492	Caco-2	colon:	n/a
49	chr11:93468466-93468516	HCT-116	colon:	n/a
50	chr11:93468442-93468492	AG09309	skin:	n/a

(count:4 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:93468648..93476533-chr11:93513626..93520226,41	K562	blood:
2	chr11:93468490..93476714-chr11:93515963..93520210,25	MCF-7	breast:
3	chr11:93431256..93433369-chr11:93468938..93470943,2	K562	blood:
4	chr11:93462890..93477443-chr11:93512595..93526939,73	K562	blood:

(count:8 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-VSTM5-1	chr11:93467791-93467826	NONHSAT023679
2	lnc-VSTM5-1	chr11:93466516-93467827	NONHSAT023666
3	lnc-VSTM5-1	chr11:93468129-93469341	NONHSAT023662
4	lnc-VSTM5-1	chr11:93467791-93467826	NONHSAT023662
5	lnc-VSTM5-1	chr11:93465410-93469014	NONHSAT023663
6	lnc-KIAA1731-1	chr11:93467787-93469469	NONHSAT023682
7	lnc-VSTM5-1	chr11:93468129-93469323	NONHSAT023671
8	lnc-VSTM5-1	chr11:93467791-93468404	NONHSAT023667

No data

Variant related genes	Relation type
SNORA8	TF binding region
SNORA40	TF binding region
SNORA1	TF binding region
SNORD5	TF binding region
SNORA18	TF binding region
SNORA25	TF binding region
SNORA32	TF binding region
TAF1D	TF binding region
SNORD6	TF binding region
MIR1304	TF binding region
SNORA8	CpG island
SNORA40	CpG island
SNORA1	CpG island
SNORD5	CpG island
SNORA18	CpG island
SNORA25	CpG island
SNORA32	CpG island
TAF1D	CpG island
SNORD6	CpG island
MIR1304	CpG island
ENSG00000166004	chromatin interactions
ENSG00000042429	chromatin interactions
ENSG00000166012	chromatin interactions
BMI1	miRNA target sites

Extended variants
information (count: 64 )
Associated
traits (count: 79 )

Variant overlapped rSNPs/rCNVs (count:64 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs532303170	chr11:93467695-93467696	Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region lncRNA	11 gene(s)	Overlapped CNVs	n/a
2	rs550806788	chr11:93467696-93467697	Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region lncRNA	11 gene(s)	Overlapped CNVs	n/a
3	rs143733388	chr11:93467736-93467737	Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region lncRNA	11 gene(s)	Overlapped CNVs	n/a
4	rs536007933	chr11:93467744-93467745	Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region lncRNA	11 gene(s)	Overlapped CNVs	n/a
5	rs548007375	chr11:93467780-93467781	Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region lncRNA	11 gene(s)	Overlapped CNVs	n/a
6	rs116789819	chr11:93467868-93467869	Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers	TF binding region Chromatin interactive region lncRNA	11 gene(s)	Overlapped CNVs	n/a
7	rs534334212	chr11:93467882-93467883	Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers	TF binding region Chromatin interactive region lncRNA	11 gene(s)	Overlapped CNVs	n/a
8	rs558668671	chr11:93467898-93467899	Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers	TF binding region Chromatin interactive region lncRNA	11 gene(s)	Overlapped CNVs	n/a
9	rs527559741	chr11:93467917-93467918	Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers	TF binding region Chromatin interactive region lncRNA	11 gene(s)	Overlapped CNVs	n/a
10	rs374105872	chr11:93467920-93467921	Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers	TF binding region Chromatin interactive region lncRNA	11 gene(s)	Overlapped CNVs	n/a
11	rs577212858	chr11:93467943-93467944	Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers	TF binding region Chromatin interactive region lncRNA	11 gene(s)	Overlapped CNVs	n/a
12	rs557583641	chr11:93467954-93467955	Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers	TF binding region Chromatin interactive region lncRNA	11 gene(s)	Overlapped CNVs	n/a
13	rs577657295	chr11:93467976-93467977	Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers	TF binding region Chromatin interactive region lncRNA	11 gene(s)	Overlapped CNVs	n/a
14	rs190664280	chr11:93467991-93467992	Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers	TF binding region Chromatin interactive region lncRNA	11 gene(s)	Overlapped CNVs	n/a
15	rs559365226	chr11:93467993-93467994	Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers	TF binding region Chromatin interactive region lncRNA	11 gene(s)	Overlapped CNVs	n/a
16	rs117981202	chr11:93468006-93468007	Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers	TF binding region Chromatin interactive region lncRNA	11 gene(s)	Overlapped CNVs	n/a
17	rs182542195	chr11:93468041-93468042	Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers	TF binding region Chromatin interactive region lncRNA	11 gene(s)	Overlapped CNVs	n/a
18	rs34650313	chr11:93468049-93468050	Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers	TF binding region Chromatin interactive region lncRNA	11 gene(s)	Overlapped CNVs	n/a
19	rs575225728	chr11:93468070-93468071	Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers	TF binding region Chromatin interactive region lncRNA	11 gene(s)	Overlapped CNVs	n/a
20	rs542419925	chr11:93468074-93468075	Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers	TF binding region Chromatin interactive region lncRNA	11 gene(s)	Overlapped CNVs	n/a
21	rs35747934	chr11:93468079-93468080	Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers	TF binding region Chromatin interactive region lncRNA	11 gene(s)	Overlapped CNVs	n/a
22	rs1063080	chr11:93468094-93468095	Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers	TF binding region Chromatin interactive region lncRNA	11 gene(s)	Overlapped CNVs	n/a
23	rs200090292	chr11:93468117-93468118	Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers	TF binding region Chromatin interactive region lncRNA	11 gene(s)	Overlapped CNVs	n/a
24	rs374603108	chr11:93468118-93468119	Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers	TF binding region Chromatin interactive region lncRNA	11 gene(s)	Overlapped CNVs	n/a
25	rs554440791	chr11:93468131-93468132	Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers	TF binding region Chromatin interactive region lncRNA	11 gene(s)	Overlapped CNVs	n/a
26	rs572843601	chr11:93468187-93468188	Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers	TF binding region Chromatin interactive region lncRNA	11 gene(s)	Overlapped CNVs	n/a
27	rs543142086	chr11:93468213-93468214	Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers	TF binding region Chromatin interactive region lncRNA	11 gene(s)	Overlapped CNVs	n/a
28	rs372957789	chr11:93468274-93468275	Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers	TF binding region Chromatin interactive region lncRNA	11 gene(s)	Overlapped CNVs	n/a
29	rs372627604	chr11:93468294-93468295	Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers	TF binding region Chromatin interactive region lncRNA	11 gene(s)	Overlapped CNVs	n/a
30	rs187246097	chr11:93468324-93468325	Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers	TF binding region Chromatin interactive region lncRNA	11 gene(s)	Overlapped CNVs	n/a
31	rs564834303	chr11:93468332-93468333	Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers	TF binding region Chromatin interactive region lncRNA	11 gene(s)	Overlapped CNVs	n/a
32	rs375872013	chr11:93468345-93468346	Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers	TF binding region Chromatin interactive region lncRNA	11 gene(s)	Overlapped CNVs	n/a
33	rs540265659	chr11:93468357-93468358	Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers	TF binding region Chromatin interactive region lncRNA	11 gene(s)	Overlapped CNVs	n/a
34	rs191868253	chr11:93468359-93468360	Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers	TF binding region Chromatin interactive region lncRNA	11 gene(s)	Overlapped CNVs	n/a
35	rs148103268	chr11:93468374-93468375	Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers	TF binding region Chromatin interactive region lncRNA	11 gene(s)	Overlapped CNVs	n/a
36	rs529962302	chr11:93468376-93468377	Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers	TF binding region Chromatin interactive region lncRNA	11 gene(s)	Overlapped CNVs	n/a
37	rs547963807	chr11:93468377-93468378	Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers	TF binding region Chromatin interactive region lncRNA	11 gene(s)	Overlapped CNVs	n/a
38	rs370000007	chr11:93468379-93468380	Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers	TF binding region Chromatin interactive region lncRNA	11 gene(s)	Overlapped CNVs	n/a
39	rs117606882	chr11:93468380-93468381	Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers	TF binding region Chromatin interactive region lncRNA	11 gene(s)	Overlapped CNVs	n/a
40	rs552592323	chr11:93468384-93468385	Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers	TF binding region Chromatin interactive region lncRNA	11 gene(s)	Overlapped CNVs	n/a
41	rs202035133	chr11:93468394-93468395	Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers	TF binding region Chromatin interactive region lncRNA	11 gene(s)	Overlapped CNVs	n/a
42	rs374381331	chr11:93468418-93468419	Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region lncRNA	12 gene(s)	Overlapped CNVs	n/a
43	rs570864365	chr11:93468421-93468422	Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region lncRNA	12 gene(s)	Overlapped CNVs	n/a
44	rs377674268	chr11:93468429-93468430	Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region lncRNA	12 gene(s)	Overlapped CNVs	n/a
45	rs57963899	chr11:93468513-93468514	Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs538784843	chr11:93468531-93468532	Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region lncRNA	12 gene(s)	Overlapped CNVs	n/a
47	rs569855769	chr11:93468543-93468544	Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region lncRNA	12 gene(s)	Overlapped CNVs	n/a
48	rs142769785	chr11:93468556-93468557	Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region lncRNA	12 gene(s)	Overlapped CNVs	n/a
49	rs377242290	chr11:93468592-93468593	Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region lncRNA	12 gene(s)	Overlapped CNVs	n/a
50	rs537247699	chr11:93468629-93468630	Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region lncRNA	12 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:79)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Wilms tumour	21544195	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Acute myeloid leukemia	20729466	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
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Cervical cancer	21062161	CNVD
Esophageal squamous carcinoma	18350619	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	22429812	CNVD
Breast cancer	16608533	CNVD
T-cell lymphomas	19863542	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Basal cell lymphoma	17053054	CNVD
Hepatocellular carcinoma	16785998	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21785460	CNVD
Cancer	22183965	CNVD
Melanoma	22183965	CNVD
Developmental delay	21147756	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21958427	CNVD
Lung cancer	18438408	CNVD
Ewing''s sarcoma	17952124	CNVD
Renal cell carcinoma	18194544	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	17133270	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Ductal carcinoma	22052326	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
Mental retardation	21062444	CNVD
Cancer	21499728	CNVD
Breast cancer	19181860	CNVD
Breast cancer	17603634	CNVD
Mantle cell lymphoma	19029149	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Basal cell lymphoma	16790693	CNVD
Breast cancer	21509527	CNVD
Prostate cancer	18632612	CNVD
Schizophrenia	23813976	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:191 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:93444800-93471000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr11:93447600-93468000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
3	chr11:93449200-93471800	Weak transcription	Right Atrium	heart
4	chr11:93449600-93471800	Weak transcription	Esophagus	oesophagus
5	chr11:93450600-93471800	Weak transcription	Gastric	stomach
6	chr11:93450600-93473000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr11:93451600-93469800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
8	chr11:93451600-93470800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
9	chr11:93453200-93468000	Strong transcription	Primary hematopoietic stem cells short term culture	blood
10	chr11:93453600-93468000	Strong transcription	Primary monocytes fromperipheralblood	blood
11	chr11:93453800-93471200	Strong transcription	Monocytes-CD14+_RO01746	blood
12	chr11:93453800-93471800	Strong transcription	Fetal Muscle Leg	muscle
13	chr11:93453800-93471800	Strong transcription	Fetal Thymus	thymus
14	chr11:93453800-93472400	Strong transcription	Fetal Muscle Trunk	muscle
15	chr11:93454000-93470400	Strong transcription	HUES48 Cell Line	embryonic stem cell
16	chr11:93454400-93467800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
17	chr11:93454400-93469000	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
18	chr11:93454400-93469400	Strong transcription	HUES64 Cell Line	embryonic stem cell
19	chr11:93454400-93469600	Strong transcription	iPS-18 Cell Line	embryonic stem cell
20	chr11:93454400-93469800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr11:93454400-93470000	Strong transcription	Primary B cells from peripheral blood	blood
22	chr11:93454400-93470800	Strong transcription	HUES6 Cell Line	embryonic stem cell
23	chr11:93454400-93471000	Strong transcription	Fetal Lung	lung
24	chr11:93454600-93471000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
25	chr11:93454600-93471000	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
26	chr11:93454800-93471000	Strong transcription	Adipose Nuclei	Adipose
27	chr11:93455000-93468000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
28	chr11:93455000-93471200	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
29	chr11:93455000-93471800	Strong transcription	Placenta	Placenta
30	chr11:93455200-93467800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
31	chr11:93457400-93470200	Strong transcription	Brain Cingulate Gyrus	brain
32	chr11:93457600-93467800	Strong transcription	Primary T cells fromperipheralblood	blood
33	chr11:93458400-93467800	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
34	chr11:93458400-93471800	Strong transcription	Stomach Smooth Muscle	stomach
35	chr11:93458600-93469400	Strong transcription	HMEC	breast
36	chr11:93458800-93467800	Strong transcription	Sigmoid Colon	Sigmoid Colon
37	chr11:93458800-93471000	Strong transcription	H1 Cell Line	embryonic stem cell
38	chr11:93458800-93471000	Strong transcription	Duodenum Smooth Muscle	Duodenum
39	chr11:93458800-93471800	Strong transcription	Skeletal Muscle Female	skeletal muscle
40	chr11:93459400-93469600	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
41	chr11:93459400-93470400	Strong transcription	Primary B cells from cord blood	blood
42	chr11:93459400-93473000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
43	chr11:93459600-93470200	Strong transcription	Cortex derived primary cultured neurospheres	brain
44	chr11:93459600-93471800	Strong transcription	Colon Smooth Muscle	Colon
45	chr11:93459800-93470800	Strong transcription	Brain Hippocampus Middle	brain
46	chr11:93460000-93468000	Strong transcription	NHLF	lung
47	chr11:93460200-93467800	Strong transcription	NHDF-Ad	bronchial
48	chr11:93460200-93468000	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
49	chr11:93460200-93468400	Strong transcription	K562	blood
50	chr11:93460200-93471000	Strong transcription	Brain Inferior Temporal Lobe	brain

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