Variant report

Variant	esv1826391
Chromosome Location	chr11:35000983-35098193
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2065)
CpG islands
(count:428)
Chromatin interactive
region (count:63)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:8)

(count:2065 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:35030945-35031794	HepG2	liver:	n/a	n/a
2	ARID3A	chr11:35061678-35062004	K562	blood:	n/a	n/a
3	ARID3A	chr11:35085029-35085388	K562	blood:	n/a	n/a
4	ARID3A	chr11:35066842-35067235	HepG2	liver:	n/a	n/a
5	ARID3A	chr11:35051547-35051772	K562	blood:	n/a	n/a
6	ARID3A	chr11:35062810-35063001	K562	blood:	n/a	n/a
7	ARID3A	chr11:35057639-35057839	K562	blood:	n/a	n/a
8	ARID3A	chr11:35050350-35050388	K562	blood:	n/a	n/a
9	ARID3A	chr11:35052064-35052688	K562	blood:	n/a	n/a
10	ARID3A	chr11:35060798-35061124	K562	blood:	n/a	n/a
11	ATF1	chr11:35088676-35088928	K562	blood:	n/a	n/a
12	ATF1	chr11:35079662-35080134	K562	blood:	n/a	n/a
13	ATF1	chr11:35084885-35085469	K562	blood:	n/a	n/a
14	ATF1	chr11:35072155-35072504	K562	blood:	n/a	n/a
15	ATF1	chr11:35069966-35070150	K562	blood:	n/a	n/a
16	ATF1	chr11:35051470-35051839	K562	blood:	n/a	n/a
17	ATF1	chr11:35057558-35057855	K562	blood:	n/a	n/a
18	ATF1	chr11:35058226-35058583	K562	blood:	n/a	n/a
19	ATF1	chr11:35052215-35052684	K562	blood:	n/a	n/a
20	ATF1	chr11:35019630-35019995	K562	blood:	n/a	n/a
21	ATF1	chr11:35061743-35062041	K562	blood:	n/a	n/a
22	ATF2	chr11:35051400-35052011	GM12878	blood:	n/a	n/a
23	ATF2	chr11:35034838-35035662	GM12878	blood:	n/a	n/a
24	ATF2	chr11:35033742-35034696	GM12878	blood:	n/a	n/a
25	ATF2	chr11:35028102-35029426	GM12878	blood:	n/a	n/a
26	ATF2	chr11:35061618-35062666	GM12878	blood:	n/a	n/a
27	ATF2	chr11:35088511-35089104	GM12878	blood:	n/a	n/a
28	ATF2	chr11:35071638-35072445	GM12878	blood:	n/a	n/a
29	ATF2	chr11:35057252-35058734	GM12878	blood:	n/a	n/a
30	ATF2	chr11:35088556-35089100	GM12878	blood:	n/a	n/a
31	ATF2	chr11:35051409-35052182	GM12878	blood:	n/a	n/a
32	ATF2	chr11:35033822-35034746	GM12878	blood:	n/a	n/a
33	ATF2	chr11:35009921-35010445	GM12878	blood:	n/a	n/a
34	ATF2	chr11:35034814-35035772	GM12878	blood:	n/a	n/a
35	ATF2	chr11:35072059-35072617	GM12878	blood:	n/a	n/a
36	ATF2	chr11:35028002-35029407	GM12878	blood:	n/a	n/a
37	ATF2	chr11:35057399-35058186	GM12878	blood:	n/a	n/a
38	ATF2	chr11:35061566-35062695	GM12878	blood:	n/a	n/a
39	ATF2	chr11:35009933-35010602	GM12878	blood:	n/a	n/a
40	ATF3	chr11:35030748-35031604	A549	lung:	n/a	n/a
41	ATF3	chr11:35030742-35031510	A549	lung:	n/a	n/a
42	ATF3	chr11:35052214-35052666	K562	blood:	n/a	n/a
43	ATF3	chr11:35061712-35062097	K562	blood:	n/a	n/a
44	ATF3	chr11:35052283-35052523	K562	blood:	n/a	n/a
45	ATF3	chr11:35051468-35051852	K562	blood:	n/a	n/a
46	BACH1	chr11:35052339-35052646	K562	blood:	n/a	n/a
47	BACH1	chr11:35062803-35062836	K562	blood:	n/a	n/a
48	BATF	chr11:35028098-35028710	GM12878	blood:	n/a	n/a
49	BATF	chr11:35051477-35051933	GM12878	blood:	n/a	chr11:35051659-35051669 chr11:35051658-35051669
50	BATF	chr11:35028835-35029269	GM12878	blood:	n/a	n/a

(count:428 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:35072710-35072760	NH-A	brain:	n/a
2	chr11:35072710-35072760	NH-A	brain:	n/a
3	chr11:35072710-35072760	SKMC	muscle:	n/a
4	chr11:35039392-35039442	ProgFib	skin:	n/a
5	chr11:35072710-35072760	SAEC	small airway:	n/a
6	chr11:35019673-35019723	MCF-7	breast:	n/a
7	chr11:35032430-35032480	ProgFib	skin:	n/a
8	chr11:35052388-35052438	NHDF-neo	bronchial:	n/a
9	chr11:35072710-35072760	GM12891	blood:	n/a
10	chr11:35032430-35032480	HCPEpiC	choroid plexus:	n/a
11	chr11:35019673-35019723	BE2_C	brain:	n/a
12	chr11:35072710-35072760	GM12892	blood:	n/a
13	chr11:35035813-35035863	PANC-1	pancreas:	n/a
14	chr11:35052388-35052438	LNCaP	prostate:	n/a
15	chr11:35035813-35035863	Hepatocyte	liver:	n/a
16	chr11:35019673-35019723	GM06990	blood:	n/a
17	chr11:35086165-35086215	K562	blood:	n/a
18	chr11:35032430-35032480	NHBE	bronchial:	n/a
19	chr11:35086165-35086215	HEEpiC	esophagus:	n/a
20	chr11:35052388-35052438	IMR90	lung:	fetal
21	chr11:35035813-35035863	LNCaP	prostate:	n/a
22	chr11:35032430-35032480	GM12892	blood:	n/a
23	chr11:35035813-35035863	GM12891	blood:	n/a
24	chr11:35039392-35039442	HRE	kidney:	n/a
25	chr11:35032430-35032480	HRE	kidney:	n/a
26	chr11:35052388-35052438	GM12891	blood:	n/a
27	chr11:35072710-35072760	NHDF-neo	bronchial:	n/a
28	chr11:35086165-35086215	SKMC	muscle:	n/a
29	chr11:35019673-35019723	SK-N-SH_RA	brain:	n/a
30	chr11:35035813-35035863	HUVEC	blood vessel:	n/a
31	chr11:35032430-35032480	PANC-1	pancreas:	n/a
32	chr11:35019673-35019723	LNCaP	prostate:	n/a
33	chr11:35039392-35039442	HEEpiC	esophagus:	n/a
34	chr11:35086165-35086215	A549	lung:	n/a
35	chr11:35086165-35086215	ovcar-3	ovarian:	n/a
36	chr11:35072710-35072760	AG04449	skin:	fetal
37	chr11:35052388-35052438	HAEpiC	amniotic membrane:	n/a
38	chr11:35072710-35072760	H1-hESC	embryonic stem cell:	embryo
39	chr11:35039392-35039442	BJ	skin:	n/a
40	chr11:35052388-35052438	SK-N-SH_RA	brain:	n/a
41	chr11:35052388-35052438	Hela-S3	cervix:	n/a
42	chr11:35039392-35039442	MCF-7	breast:	n/a
43	chr11:35039392-35039442	AG04449	skin:	fetal
44	chr11:35052388-35052438	HCF	heart:	n/a
45	chr11:35052388-35052438	A549	lung:	n/a
46	chr11:35072710-35072760	AG09309	skin:	n/a
47	chr11:35032430-35032480	HPAEpiC	pulmonary alveolar:	n/a
48	chr11:35032430-35032480	HRCEpiC	kidney:	n/a
49	chr11:35052388-35052438	Jurkat	blood:	n/a
50	chr11:35086165-35086215	PrEC	prostate:	n/a

(count:63 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr11:35052336..35054064-chr11:35054789..35057693,2	K562	blood:
2	chr11:35023109..35024756-chr11:35037668..35039573,2	K562	blood:
3	chr11:35058680..35060384-chr11:35065548..35067389,2	MCF-7	breast:
4	chr11:35020698..35022815-chr11:35039638..35042046,2	K562	blood:
5	chr11:35039282..35042124-chr11:35049320..35051716,2	MCF-7	breast:
6	chr11:35087035..35089860-chr11:35091064..35093898,2	MCF-7	breast:
7	chr11:35023109..35024756-chr11:35037668..35039573,2	K562	blood:
8	chr11:35039282..35042124-chr11:35049320..35051716,2	MCF-7	breast:
9	chr11:35021693..35023212-chr11:35050497..35053250,2	MCF-7	breast:
10	chr11:35087035..35089860-chr11:35091064..35093898,2	MCF-7	breast:
11	chr11:34989938..34992204-chr11:35000945..35002458,2	K562	blood:
12	chr11:35028741..35031427-chr11:35032787..35035913,3	K562	blood:
13	chr11:35060552..35062107-chr11:35062837..35064622,2	MCF-7	breast:
14	chr11:35015301..35017003-chr11:35017978..35019593,2	MCF-7	breast:
15	chr11:34948435..34950390-chr11:35072380..35075148,2	K562	blood:
16	chr11:35054850..35057258-chr11:35063545..35065206,3	MCF-7	breast:
17	chr11:35056767..35059035-chr11:35065294..35067500,2	K562	blood:
18	chr11:35058680..35060384-chr11:35065548..35067389,2	MCF-7	breast:
19	chr11:35019170..35019966-chr11:35413526..35414443,3	MCF-7	breast:
20	chr11:35059235..35060888-chr11:35161011..35163300,2	MCF-7	breast:
21	chr11:35028741..35031427-chr11:35032787..35035913,3	K562	blood:
22	chr11:35060552..35062107-chr11:35062837..35064622,2	MCF-7	breast:
23	chr11:35054850..35057258-chr11:35063545..35065206,3	MCF-7	breast:
24	chr11:35054364..35057868-chr11:35058147..35061755,3	K562	blood:
25	chr11:35097231..35099674-chr11:35101240..35103980,3	K562	blood:
26	chr11:35038263..35041721-chr11:35159851..35162201,3	MCF-7	breast:
27	chr11:35011432..35012993-chr11:35018047..35020320,2	K562	blood:
28	chr11:35026581..35028709-chr11:35030070..35032050,2	K562	blood:
29	chr11:35050379..35055023-chr11:35058548..35063780,5	MCF-7	breast:
30	chr11:35021693..35023212-chr11:35050497..35053250,2	MCF-7	breast:
31	chr11:35054364..35057868-chr11:35058147..35061755,3	K562	blood:
32	chr11:35011432..35012993-chr11:35018047..35020320,2	K562	blood:
33	chr11:35055142..35056681-chr11:35058687..35060261,2	MCF-7	breast:
34	chr11:34937971..34939750-chr11:35062496..35064603,2	K562	blood:
35	chr11:35056767..35059035-chr11:35065294..35067500,2	K562	blood:
36	chr11:35086278..35088027-chr11:35090428..35092324,3	K562	blood:
37	chr11:35086278..35088027-chr11:35090428..35092324,3	K562	blood:
38	chr11:35058493..35060030-chr11:35060277..35061819,2	K562	blood:
39	chr11:35050517..35052677-chr11:35065091..35067302,2	K562	blood:
40	chr11:35027303..35029685-chr11:35029694..35032602,2	MCF-7	breast:
41	chr11:35050379..35055023-chr11:35058548..35063780,5	MCF-7	breast:
42	chr11:35022176..35024794-chr17:57830885..57833390,2	MCF-7	breast:
43	chr11:35052321..35054037-chr11:35088777..35091263,2	K562	blood:
44	chr11:35056143..35059924-chr11:35060338..35062648,3	MCF-7	breast:
45	chr11:35083507..35086389-chr11:35411165..35412873,2	MCF-7	breast:
46	chr1:121484265..121484831-chr11:35019171..35020047,2	MCF-7	breast:
47	chr11:35052321..35054037-chr11:35088777..35091263,2	K562	blood:
48	chr11:35039461..35041795-chr11:35050641..35052600,2	K562	blood:
49	chr11:35027303..35029685-chr11:35029694..35032602,2	MCF-7	breast:
50	chr11:35026796..35028891-chr11:35159653..35162331,2	MCF-7	breast:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PDHX-3	chr11:35071626-35071672	NONHSAT018768
2	lnc-APIP-1	chr11:35086673-35086860	XLOC_009415
3	lnc-APIP-1	chr11:35086667-35086860	NONHSAT018769
4	lnc-APIP-1	chr11:35088226-35088723	NONHSAT018769
5	lnc-APIP-1	chr11:35080723-35081531	NONHSAT018769
6	lnc-APIP-1	chr11:35095464-35095505	XLOC_009415

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location
1	PDHX	hsa-miR-26b-5p	chr11:35017173-35017194
2	PDHX	hsa-miR-181b-5p	chr11:35017036-35017058
3	PDHX	hsa-miR-181d-5p	chr11:35017036-35017058
4	PDHX	hsa-miR-29c-3p	chr11:35016971-35016977
5	PDHX	hsa-miR-181d-5p	chr11:35017367-35017389
6	PDHX	hsa-miR-26b-5p	chr11:35017187-35017194
7	PDHX	hsa-miR-181b-5p	chr11:35017369-35017389
8	PDHX	hsa-miR-29c-3p	chr11:35016953-35016978

Variant related genes	Relation type
PDHX	TF binding region
PDHX	CpG island
ENSG00000149089	chromatin interactions
ENSG00000026508	chromatin interactions
ENSG00000110435	chromatin interactions
CUEDC2	miRNA target sites
GANAB	miRNA target sites

Extended variants
information (count: 3874 )
Associated
traits (count: 80 )

Variant overlapped rSNPs/rCNVs (count:3874 , 50 per page) page: 1 2 3 4 5 6 7 ... 78

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2767038	chr11:35000983-35000984	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs376287163	chr11:35000990-35000991	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs543276089	chr11:35000998-35000999	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs182771149	chr11:35001144-35001145	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs560475385	chr11:35001161-35001162	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs57376219	chr11:35001163-35001164	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs549201064	chr11:35001180-35001181	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs576959424	chr11:35001295-35001296	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs568930177	chr11:35001308-35001309	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs537958415	chr11:35001346-35001347	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs117948785	chr11:35001437-35001438	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs374372444	chr11:35001463-35001464	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs533595033	chr11:35001472-35001473	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs115307091	chr11:35001473-35001474	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs573999728	chr11:35001480-35001481	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs61882167	chr11:35001496-35001497	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs556356611	chr11:35001626-35001627	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs189023826	chr11:35001631-35001632	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs576431434	chr11:35001660-35001661	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs545463251	chr11:35001688-35001689	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs565269592	chr11:35001690-35001691	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs199924363	chr11:35001697-35001698	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs144945918	chr11:35001699-35001700	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs72181575	chr11:35001700-35001701	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs71457366	chr11:35001702-35001703	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs200938713	chr11:35001703-35001704	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs572395456	chr11:35001710-35001711	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs11032964	chr11:35001746-35001747	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs141317522	chr11:35001772-35001773	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs12792494	chr11:35001825-35001826	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs529210634	chr11:35001829-35001830	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs193024857	chr11:35001841-35001842	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs569040456	chr11:35001879-35001880	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs57927359	chr11:35001913-35001914	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs371392925	chr11:35001939-35001940	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs531432168	chr11:35002036-35002037	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs551450063	chr11:35002100-35002101	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs571304207	chr11:35002127-35002128	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs372697771	chr11:35002146-35002147	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs151002383	chr11:35002158-35002159	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs372596661	chr11:35002186-35002187	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs567586445	chr11:35002195-35002196	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs377045039	chr11:35002242-35002243	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs536571080	chr11:35002245-35002246	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs184065449	chr11:35002260-35002261	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs369646215	chr11:35002279-35002280	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs570215566	chr11:35002301-35002302	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs140453363	chr11:35002434-35002435	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs538903063	chr11:35002471-35002472	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs2767039	chr11:35002529-35002530	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance

Variant related diseases (count:80)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Medulloblastoma	21979893	CNVD
Thyroid cancer	19087340	CNVD
Melanoma	18172304	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Wilms tumour	21544195	CNVD
Parathyroid adenoma	22454399	CNVD
Chordoma	21602918	CNVD
Breast cancer	21949216	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	19222835	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Beckwith-Wiedemann syndrome	21518781	CNVD
Wilms tumour	21518781	CNVD
Hepatoblastoma	21518781	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Gastric cancer	17908304	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Multiple myeloma	20724749	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Autism	22495311	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	21785460	CNVD
Medulloblastoma	16783165	CNVD
small cell lung cancer	20016488	CNVD
Renal cell carcinoma	18194544	CNVD
Potocki-Shaffer syndrome	19222835	CNVD
WAGR syndrome	19222835	CNVD
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Glioblastoma multiforme	22286061	CNVD
Breast cancer	21364760	CNVD
Aniridia syndrome	21572526	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16272173	CNVD
Retinoblastoma	22278416	CNVD
Denys-drash syndrome	21085971	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
WAGR syndrome	16773131	CNVD
Disorders of sex development	22290220	CNVD
Aniridia syndrome	17204608	CNVD
Mental retardation	17204608	CNVD
WAGR syndrome	19617690	CNVD
genitourinary abnormalities	17204608	CNVD
Breast cancer	16397240	CNVD
Mental retardation	16773131	CNVD
Multiple myeloma	16616336	CNVD
Cancer	17160897	CNVD
Cancer	21183584	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
WAGR syndrome	22470819	CNVD
Neurodevelopmental disorder	22521361	CNVD
Denys-drash syndrome	19566914	CNVD
Familial wilms tumor	19566914	CNVD
Frasier syndrome	19566914	CNVD
Non-small cell lung cancer	21829676	CNVD
WAGR syndrome	20603712	CNVD
Autism	17322880	CNVD
Renal cell carcinoma	18765545	CNVD
Breast cancer	21858162	CNVD
Cancer	20164920	CNVD
Breast cancer	16620391	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:2395 , 50 per page) page: 1 2 3 4 5 6 7 ... 48

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:34948000-35006800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
2	chr11:34952200-35010800	Weak transcription	Small Intestine	intestine
3	chr11:34959000-35019600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
4	chr11:34962000-35008200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
5	chr11:34962800-35006600	Weak transcription	Esophagus	oesophagus
6	chr11:34965400-35008200	Weak transcription	Gastric	stomach
7	chr11:34975400-35006800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
8	chr11:34976600-35018400	Weak transcription	Spleen	Spleen
9	chr11:34977800-35009800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
10	chr11:34981600-35006000	Weak transcription	Brain Anterior Caudate	brain
11	chr11:34982200-35014200	Weak transcription	Fetal Brain Male	brain
12	chr11:34983400-35006800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
13	chr11:34983400-35008200	Weak transcription	Aorta	Aorta
14	chr11:34983600-35018200	Weak transcription	H9 Cell Line	embryonic stem cell
15	chr11:34984800-35001000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
16	chr11:34985200-35026600	Weak transcription	Colonic Mucosa	Colon
17	chr11:34987000-35008200	Weak transcription	Pancreas	Pancrea
18	chr11:34987000-35017000	Weak transcription	K562	blood
19	chr11:34988800-35001000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
20	chr11:34988800-35006200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
21	chr11:34991000-35020800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
22	chr11:34991800-35005600	Weak transcription	Placenta	Placenta
23	chr11:34991800-35006600	Weak transcription	Fetal Intestine Small	intestine
24	chr11:34992200-35002600	Weak transcription	H1 Cell Line	embryonic stem cell
25	chr11:34992400-35002200	Weak transcription	Fetal Thymus	thymus
26	chr11:34992400-35004800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
27	chr11:34992400-35009400	Weak transcription	GM12878-XiMat	blood
28	chr11:34992400-35016600	Weak transcription	Fetal Heart	heart
29	chr11:34992600-35006200	Weak transcription	Duodenum Mucosa	Duodenum
30	chr11:34992600-35006200	Weak transcription	Fetal Brain Female	brain
31	chr11:34993000-35002000	Weak transcription	Brain Germinal Matrix	brain
32	chr11:34994200-35006000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
33	chr11:34996800-35001000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
34	chr11:34997200-35001000	Enhancers	HSMMtube	muscle
35	chr11:34997600-35019600	Weak transcription	Fetal Kidney	kidney
36	chr11:34997800-35006000	Weak transcription	Fetal Muscle Trunk	muscle
37	chr11:34998200-35001000	Strong transcription	Liver	Liver
38	chr11:34998400-35001000	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
39	chr11:34998600-35001000	Strong transcription	Dnd41	blood
40	chr11:34998600-35006800	Weak transcription	Primary neutrophils fromperipheralblood	blood
41	chr11:34998800-35001000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
42	chr11:34999000-35001000	Strong transcription	Duodenum Smooth Muscle	Duodenum
43	chr11:34999000-35005800	Weak transcription	Cortex derived primary cultured neurospheres	brain
44	chr11:34999000-35006000	Weak transcription	HUES6 Cell Line	embryonic stem cell
45	chr11:34999000-35018600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
46	chr11:34999400-35001000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
47	chr11:34999600-35001000	Enhancers	Muscle Satellite Cultured Cells	--
48	chr11:34999600-35001000	Genic enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
49	chr11:34999600-35001000	Enhancers	HUVEC	blood vessel
50	chr11:34999600-35001200	Strong transcription	Breast Myoepithelial Primary Cells	Breast

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