Variant report

Variant	esv3424593
Chromosome Location	chr11:34071901-34074749
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:901)
CpG islands
(count:673)
Chromatin interactive
region (count:22)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:901 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:34072962-34073385	HepG2	liver:	n/a	n/a
2	ARID3A	chr11:34073832-34074025	K562	blood:	n/a	n/a
3	ATF2	chr11:34074685-34075378	GM12878	blood:	n/a	n/a
4	ATF2	chr11:34073628-34074160	GM12878	blood:	n/a	n/a
5	ATF2	chr11:34073749-34074066	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr11:34072850-34073351	GM12878	blood:	n/a	n/a
7	ATF3	chr11:34072875-34073379	A549	lung:	n/a	n/a
8	BACH1	chr11:34073725-34073954	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr11:34073036-34073486	K562	blood:	n/a	n/a
10	BACH1	chr11:34073031-34073522	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr11:34071966-34072143	K562	blood:	n/a	n/a
12	BACH1	chr11:34074586-34075063	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr11:34073777-34073977	K562	blood:	n/a	n/a
14	BATF	chr11:34073695-34074015	GM12878	blood:	n/a	n/a
15	BCL3	chr11:34074622-34075257	A549	lung:	n/a	chr11:34074920-34074929 chr11:34075022-34075035
16	BCL3	chr11:34073621-34074216	A549	lung:	n/a	chr11:34073654-34073667
17	BCL3	chr11:34072828-34073491	A549	lung:	n/a	chr11:34073173-34073186
18	BCL3	chr11:34074487-34075045	A549	lung:	n/a	chr11:34074920-34074929 chr11:34075022-34075035
19	BCLAF1	chr11:34072829-34073506	K562	blood:	n/a	chr11:34073173-34073186
20	BCLAF1	chr11:34073575-34074178	K562	blood:	n/a	chr11:34073654-34073667
21	BCLAF1	chr11:34073735-34074027	GM12878	blood:	n/a	n/a
22	BCLAF1	chr11:34072802-34073518	GM12878	blood:	n/a	chr11:34073173-34073186
23	BCLAF1	chr11:34073551-34074139	GM12878	blood:	n/a	chr11:34073654-34073667
24	BCLAF1	chr11:34074192-34074634	GM12878	blood:	n/a	n/a
25	BCLAF1	chr11:34074616-34075434	GM12878	blood:	n/a	chr11:34074920-34074929 chr11:34075022-34075035
26	BHLHE40	chr11:34072986-34074086	GM12878	blood:	n/a	chr11:34073259-34073275
27	BHLHE40	chr11:34073667-34074054	HepG2	liver:	n/a	n/a
28	BHLHE40	chr11:34072627-34074539	K562	blood:	n/a	chr11:34073259-34073275
29	BRCA1	chr11:34073093-34073449	HepG2	liver:	n/a	n/a
30	BRCA1	chr11:34072938-34073374	Hela-S3	cervix:	n/a	n/a
31	BRCA1	chr11:34074456-34074516	Hela-S3	cervix:	n/a	n/a
32	BRCA1	chr11:34073813-34074075	Hela-S3	cervix:	n/a	n/a
33	CBX3	chr11:34072809-34073690	K562	blood:	n/a	n/a
34	CBX3	chr11:34073702-34074168	K562	blood:	n/a	n/a
35	CCNT2	chr11:34072752-34074678	K562	blood:	n/a	chr11:34073113-34073122 chr11:34072908-34072917 chr11:34073837-34073846 chr11:34073527-34073536 chr11:34072914-34072923 chr11:34072901-34072910
36	CEBPB	chr11:34072500-34073279	GM12878	blood:	n/a	n/a
37	CEBPB	chr11:34073818-34074069	H1-hESC	embryonic stem cell:	n/a	n/a
38	CEBPB	chr11:34072964-34073255	Hela-S3	cervix:	n/a	n/a
39	CEBPB	chr11:34073774-34074012	GM12878	blood:	n/a	n/a
40	CEBPD	chr11:34073012-34073496	K562	blood:	n/a	n/a
41	CEBPD	chr11:34073119-34073391	HepG2	liver:	n/a	n/a
42	CEBPD	chr11:34072874-34074056	HepG2	liver:	n/a	n/a
43	CHD1	chr11:34073635-34075733	H1-hESC	embryonic stem cell:	n/a	n/a
44	CHD1	chr11:34073027-34073428	H1-hESC	embryonic stem cell:	n/a	n/a
45	CHD1	chr11:34072421-34075781	IMR90	lung:	n/a	n/a
46	CHD1	chr11:34072595-34073415	GM12878	blood:	n/a	n/a
47	CHD1	chr11:34073633-34075715	GM12878	blood:	n/a	n/a
48	CHD1	chr11:34072629-34072764	H1-hESC	embryonic stem cell:	n/a	n/a
49	CHD2	chr11:34072676-34075278	Hela-S3	cervix:	n/a	n/a
50	CHD2	chr11:34073604-34074115	H1-hESC	embryonic stem cell:	n/a	n/a

(count:673 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:34073025-34073075	AG04449	skin:	fetal
2	chr11:34073162-34073212	ovcar-3	ovarian:	n/a
3	chr11:34073025-34073075	AG04449	skin:	fetal
4	chr11:34073162-34073212	ovcar-3	ovarian:	n/a
5	chr11:34073324-34073374	MCF10A-Er-Src	breast:	n/a
6	chr11:34073487-34073537	SK-N-SH	brain:	n/a
7	chr11:34073487-34073537	H1-hESC	embryonic stem cell:	embryo
8	chr11:34072820-34072870	HRPEpiC	eye:	n/a
9	chr11:34073162-34073212	CMK	blood:	n/a
10	chr11:34073487-34073537	HRCEpiC	kidney:	n/a
11	chr11:34072820-34072870	HEEpiC	esophagus:	n/a
12	chr11:34074141-34074191	CMK	blood:	n/a
13	chr11:34074141-34074191	AG04450	lung:	fetal
14	chr11:34073025-34073075	SK-N-SH_RA	brain:	n/a
15	chr11:34073162-34073212	LNCaP	prostate:	n/a
16	chr11:34073070-34073120	Jurkat	blood:	n/a
17	chr11:34073061-34073111	Hela-S3	cervix:	n/a
18	chr11:34072820-34072870	GM12891	blood:	n/a
19	chr11:34073061-34073111	HCT-116	colon:	n/a
20	chr11:34073070-34073120	H1-hESC	embryonic stem cell:	embryo
21	chr11:34074141-34074191	NHBE	bronchial:	n/a
22	chr11:34074141-34074191	AG09319	gingival:	n/a
23	chr11:34073324-34073374	K562	blood:	n/a
24	chr11:34073324-34073374	HPAEpiC	pulmonary alveolar:	n/a
25	chr11:34073487-34073537	GM12892	blood:	n/a
26	chr11:34073002-34073052	HPAEpiC	pulmonary alveolar:	n/a
27	chr11:34073002-34073052	SAEC	small airway:	n/a
28	chr11:34073002-34073052	MCF-7	breast:	n/a
29	chr11:34073162-34073212	ECC-1	luminal epithelium:	n/a
30	chr11:34073487-34073537	ECC-1	luminal epithelium:	n/a
31	chr11:34072820-34072870	MCF-7	breast:	n/a
32	chr11:34073216-34073266	T-47D	breast:	n/a
33	chr11:34074702-34074752	NB4	blood:	n/a
34	chr11:34073162-34073212	Hepatocyte	liver:	n/a
35	chr11:34074702-34074752	SK-N-SH	brain:	n/a
36	chr11:34073324-34073374	BJ	skin:	n/a
37	chr11:34073216-34073266	NHDF-neo	bronchial:	n/a
38	chr11:34073324-34073374	HepG2	liver:	n/a
39	chr11:34073487-34073537	AG04449	skin:	fetal
40	chr11:34074702-34074752	HRPEpiC	eye:	n/a
41	chr11:34073002-34073052	HMEC	breast:	n/a
42	chr11:34073061-34073111	HRCEpiC	kidney:	n/a
43	chr11:34073002-34073052	HL-60	blood:	n/a
44	chr11:34073025-34073075	SK-N-MC	brain:	n/a
45	chr11:34073324-34073374	HAEpiC	amniotic membrane:	n/a
46	chr11:34074702-34074752	GM12891	blood:	n/a
47	chr11:34073002-34073052	BJ	skin:	n/a
48	chr11:34073324-34073374	NB4	blood:	n/a
49	chr11:34074702-34074752	IMR90	lung:	fetal
50	chr11:34073002-34073052	AG10803	skin:	n/a

(count:22 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:33279061..33281281-chr11:34073248..34075291,2	K562	blood:
2	chr11:34073129..34073642-chr11:61584311..61584940,2	Hela-S3	cervix:
3	chr11:34072138..34074908-chr17:56707935..56709645,2	MCF-7	breast:
4	chr11:34073154..34074985-chr11:34112117..34113904,3	K562	blood:
5	chr11:34070943..34077471-chr11:34125498..34130034,9	MCF-7	breast:
6	chr11:34073154..34075111-chr11:34112117..34115103,4	K562	blood:
7	chr11:34073196..34074070-chr6:30539019..30539630,2	HCT-116	colon:
8	chr11:10830071..10830798-chr11:34073504..34074175,2	HCT-116	colon:
9	chr11:34071305..34076629-chr11:34124370..34130035,10	MCF-7	breast:
10	chr11:34073237..34073837-chr15:42565350..42566240,2	Hela-S3	cervix:
11	chr11:34042157..34043774-chr11:34070520..34073015,2	MCF-7	breast:
12	chr11:34072129..34073643-chr11:34109400..34112113,2	MCF-7	breast:
13	chr11:34072006..34079358-chr11:34124269..34129390,19	K562	blood:
14	chr11:34073078..34074014-chr2:85829316..85830023,2	HCT-116	colon:
15	chr11:34073205..34075094-chr11:34377742..34380453,3	MCF-7	breast:
16	chr11:34068673..34076707-chr11:34122442..34129826,21	K562	blood:
17	chr1:149222363..149225341-chr11:34071940..34074204,2	MCF-7	breast:
18	chr11:34073528..34074385-chr16:30456695..30457280,2	NB4	blood:
19	chr11:34072966..34075629-chr11:34112119..34114294,2	MCF-7	breast:
20	chr10:101380629..101381196-chr11:34073799..34074523,2	Hela-S3	cervix:
21	chr11:34071981..34076766-chr11:34377622..34383038,7	MCF-7	breast:
22	chr11:34074052..34075664-chr12:52445107..52446753,2	MCF-7	breast:

No data

Variant related genes	Relation type
CAPRIN1	TF binding region
CAPRIN1	CpG island
ENSG00000135387	chromatin interactions
ENSG00000212195	chromatin interactions
ENSG00000149485	chromatin interactions
ENSG00000179918	chromatin interactions
ENSG00000260475	chromatin interactions
ENSG00000204574	chromatin interactions
ENSG00000135372	chromatin interactions
ENSG00000206737	chromatin interactions
ENSG00000110321	chromatin interactions
ENSG00000123358	chromatin interactions
ENSG00000214013	chromatin interactions
ENSG00000103978	chromatin interactions
ENSG00000110422	chromatin interactions
ENSG00000168890	chromatin interactions
ENSG00000166016	chromatin interactions
ENSG00000168883	chromatin interactions

Extended variants
information (count: 132 )
Associated
traits (count: 79 )

Variant overlapped rSNPs/rCNVs (count:132 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs111264868	chr11:34071925-34071926	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs566033413	chr11:34072009-34072010	Flanking Active TSS Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs12418412	chr11:34072011-34072012	Flanking Active TSS Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs548619027	chr11:34072014-34072015	Flanking Active TSS Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs374962825	chr11:34072066-34072067	Flanking Active TSS Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs193243673	chr11:34072072-34072073	Flanking Active TSS Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs568213009	chr11:34072101-34072102	Flanking Active TSS Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs35815611	chr11:34072111-34072112	Flanking Active TSS Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs184085603	chr11:34072140-34072141	Flanking Active TSS Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
10	rs372778048	chr11:34072164-34072165	Flanking Active TSS Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
11	rs549548960	chr11:34072196-34072197	Flanking Active TSS Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
12	rs569536920	chr11:34072217-34072218	Flanking Active TSS Weak transcription Active TSS Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
13	rs563218362	chr11:34072222-34072223	Flanking Active TSS Weak transcription Active TSS Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
14	rs538890391	chr11:34072257-34072258	Flanking Active TSS Weak transcription Active TSS Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
15	rs558585216	chr11:34072272-34072273	Flanking Active TSS Weak transcription Active TSS Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
16	rs571959964	chr11:34072289-34072290	Flanking Active TSS Weak transcription Active TSS Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
17	rs138593186	chr11:34072294-34072295	Flanking Active TSS Weak transcription Active TSS Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
18	rs76973274	chr11:34072325-34072326	Flanking Active TSS Weak transcription Active TSS Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
19	rs75638320	chr11:34072354-34072355	Flanking Active TSS Weak transcription Active TSS Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
20	rs543568355	chr11:34072356-34072357	Flanking Active TSS Weak transcription Active TSS Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
21	rs563847565	chr11:34072403-34072404	Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
22	rs577532434	chr11:34072409-34072410	Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
23	rs546438633	chr11:34072445-34072446	Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
24	rs559800136	chr11:34072465-34072466	Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
25	rs528828341	chr11:34072483-34072484	Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
26	rs7125948	chr11:34072538-34072539	Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs527827865	chr11:34072555-34072556	Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
28	rs554036052	chr11:34072583-34072584	Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
29	rs113163551	chr11:34072585-34072586	Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
30	rs552386670	chr11:34072591-34072592	Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
31	rs116408939	chr11:34072767-34072768	Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
32	rs187192416	chr11:34072785-34072786	Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
33	rs113439597	chr11:34072804-34072805	Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
34	rs73497021	chr11:34072812-34072813	Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs552393686	chr11:34072829-34072830	Active TSS Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
36	rs565824664	chr11:34072868-34072869	Active TSS Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
37	rs574196551	chr11:34072907-34072908	Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
38	rs570688314	chr11:34072915-34072916	Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
39	rs192124278	chr11:34072934-34072935	Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
40	rs144649684	chr11:34072966-34072967	Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
41	rs534950134	chr11:34072997-34072998	Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
42	rs554581429	chr11:34073013-34073014	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
43	rs574509613	chr11:34073020-34073021	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
44	rs537112040	chr11:34073071-34073072	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
45	rs557103907	chr11:34073088-34073089	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
46	rs577323604	chr11:34073092-34073093	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
47	rs546079054	chr11:34073102-34073103	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
48	rs559938907	chr11:34073116-34073117	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
49	rs573443135	chr11:34073128-34073129	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
50	rs369791122	chr11:34073148-34073149	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:79)

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
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:386 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:34066400-34072600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr11:34066800-34072000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr11:34066800-34072200	Weak transcription	Primary neutrophils fromperipheralblood	blood
4	chr11:34067000-34072000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
5	chr11:34067000-34072200	Weak transcription	GM12878-XiMat	blood
6	chr11:34067000-34072400	Weak transcription	H9 Cell Line	embryonic stem cell
7	chr11:34067200-34072000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
8	chr11:34067200-34072000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
9	chr11:34067200-34072000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
10	chr11:34067200-34072000	Weak transcription	Stomach Mucosa	stomach
11	chr11:34067200-34072400	Weak transcription	Placenta Amnion	Placenta Amnion
12	chr11:34067200-34072600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
13	chr11:34067400-34072000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
14	chr11:34067400-34072000	Weak transcription	HUES64 Cell Line	embryonic stem cell
15	chr11:34067400-34072200	Weak transcription	HUVEC	blood vessel
16	chr11:34067600-34072000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
17	chr11:34067600-34072000	Weak transcription	A549	lung
18	chr11:34067800-34072200	Weak transcription	Primary T helper cells fromperipheralblood	blood
19	chr11:34068200-34072200	Weak transcription	Fetal Brain Male	brain
20	chr11:34070400-34072000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr11:34070600-34072600	Enhancers	Placenta	Placenta
22	chr11:34071200-34072200	Weak transcription	Primary monocytes fromperipheralblood	blood
23	chr11:34071200-34072200	Weak transcription	Monocytes-CD14+_RO01746	blood
24	chr11:34071600-34072000	Enhancers	ES-I3 Cell Line	embryonic stem cell
25	chr11:34071600-34072200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr11:34071600-34072200	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr11:34071600-34072200	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr11:34071600-34072200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
29	chr11:34071600-34072200	Enhancers	HepG2	liver
30	chr11:34071600-34072200	Enhancers	NHEK	skin
31	chr11:34071600-34072400	Enhancers	Breast Myoepithelial Primary Cells	Breast
32	chr11:34071600-34072400	Enhancers	Adipose Nuclei	Adipose
33	chr11:34071600-34072400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
34	chr11:34071600-34072400	Enhancers	Fetal Intestine Small	intestine
35	chr11:34071600-34072400	Enhancers	HSMMtube	muscle
36	chr11:34071600-34072400	Enhancers	Osteobl	bone
37	chr11:34071800-34072000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
38	chr11:34071800-34072000	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
39	chr11:34071800-34072000	Active TSS	iPS-18 Cell Line	embryonic stem cell
40	chr11:34071800-34072000	Enhancers	Muscle Satellite Cultured Cells	--
41	chr11:34071800-34072000	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
42	chr11:34071800-34072000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
43	chr11:34071800-34072000	Enhancers	Aorta	Aorta
44	chr11:34071800-34072000	Enhancers	Esophagus	oesophagus
45	chr11:34071800-34072000	Enhancers	Right Atrium	heart
46	chr11:34071800-34072000	Enhancers	Stomach Smooth Muscle	stomach
47	chr11:34071800-34072000	Enhancers	Dnd41	blood
48	chr11:34071800-34072200	Enhancers	HUES6 Cell Line	embryonic stem cell
49	chr11:34071800-34072200	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
50	chr11:34071800-34072200	Enhancers	Primary hematopoietic stem cells	blood

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