Variant report

Variant	esv2753052
Chromosome Location	chr11:34247462-34358300
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1983)
CpG islands
(count:794)
Chromatin interactive
region (count:114)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1983 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:34338651-34338851	HepG2	liver:	n/a	n/a
2	ARID3A	chr11:34354251-34354423	HepG2	liver:	n/a	n/a
3	ARID3A	chr11:34339955-34340500	HepG2	liver:	n/a	n/a
4	ARID3A	chr11:34330729-34331219	HepG2	liver:	n/a	n/a
5	ARID3A	chr11:34263663-34263838	K562	blood:	n/a	n/a
6	ARID3A	chr11:34272488-34272500	K562	blood:	n/a	n/a
7	ARID3A	chr11:34258144-34258360	K562	blood:	n/a	n/a
8	ARID3A	chr11:34331458-34331706	HepG2	liver:	n/a	n/a
9	ATF1	chr11:34258159-34258470	K562	blood:	n/a	n/a
10	ATF1	chr11:34263622-34264047	K562	blood:	n/a	n/a
11	ATF1	chr11:34264548-34264774	K562	blood:	n/a	n/a
12	ATF1	chr11:34271202-34271360	K562	blood:	n/a	n/a
13	ATF1	chr11:34255636-34255924	K562	blood:	n/a	n/a
14	ATF2	chr11:34324042-34324553	GM12878	blood:	n/a	n/a
15	ATF2	chr11:34265540-34266147	GM12878	blood:	n/a	n/a
16	ATF2	chr11:34253173-34253663	GM12878	blood:	n/a	n/a
17	ATF2	chr11:34255540-34255940	H1-hESC	embryonic stem cell:	n/a	n/a
18	ATF2	chr11:34323938-34324575	GM12878	blood:	n/a	n/a
19	ATF2	chr11:34256641-34257339	GM12878	blood:	n/a	n/a
20	ATF2	chr11:34265488-34266211	GM12878	blood:	n/a	n/a
21	ATF2	chr11:34261244-34261828	GM12878	blood:	n/a	n/a
22	ATF2	chr11:34263526-34263963	GM12878	blood:	n/a	n/a
23	ATF2	chr11:34255499-34256159	GM12878	blood:	n/a	n/a
24	ATF2	chr11:34256665-34257227	GM12878	blood:	n/a	n/a
25	ATF2	chr11:34255380-34256269	GM12878	blood:	n/a	n/a
26	ATF3	chr11:34264947-34265689	A549	lung:	n/a	n/a
27	ATF3	chr11:34296192-34296750	A549	lung:	n/a	chr11:34296469-34296480 chr11:34296470-34296481 chr11:34296467-34296480 chr11:34296459-34296479 chr11:34296471-34296481 chr11:34296467-34296482 chr11:34296470-34296478 chr11:34296468-34296478 chr11:34296467-34296478 chr11:34296469-34296482 chr11:34296471-34296478 chr11:34296468-34296481
28	BACH1	chr11:34337547-34337584	H1-hESC	embryonic stem cell:	n/a	n/a
29	BACH1	chr11:34255562-34255974	H1-hESC	embryonic stem cell:	n/a	n/a
30	BACH1	chr11:34265215-34265539	H1-hESC	embryonic stem cell:	n/a	n/a
31	BATF	chr11:34265565-34266061	GM12878	blood:	n/a	n/a
32	BATF	chr11:34256722-34257234	GM12878	blood:	n/a	n/a
33	BATF	chr11:34265298-34266102	GM12878	blood:	n/a	n/a
34	BATF	chr11:34253222-34253532	GM12878	blood:	n/a	n/a
35	BATF	chr11:34323976-34324512	GM12878	blood:	n/a	chr11:34324172-34324182
36	BATF	chr11:34324025-34324515	GM12878	blood:	n/a	chr11:34324172-34324182
37	BATF	chr11:34270025-34270281	GM12878	blood:	n/a	n/a
38	BATF	chr11:34256617-34257256	GM12878	blood:	n/a	n/a
39	BATF	chr11:34356950-34357188	GM12878	blood:	n/a	n/a
40	BATF	chr11:34255571-34256220	GM12878	blood:	n/a	n/a
41	BATF	chr11:34261472-34261820	GM12878	blood:	n/a	n/a
42	BCL11A	chr11:34255701-34256085	GM12878	blood:	n/a	chr11:34255960-34255969 chr11:34255961-34255970
43	BCL11A	chr11:34256644-34257202	GM12878	blood:	n/a	n/a
44	BCL11A	chr11:34261392-34261842	GM12878	blood:	n/a	chr11:34261556-34261565
45	BCL11A	chr11:34253175-34253472	GM12878	blood:	n/a	n/a
46	BCL11A	chr11:34324042-34324477	GM12878	blood:	n/a	chr11:34324174-34324183 chr11:34324175-34324184
47	BCL11A	chr11:34265602-34266021	GM12878	blood:	n/a	n/a
48	BCL11A	chr11:34255514-34256163	GM12878	blood:	n/a	chr11:34255960-34255969 chr11:34255961-34255970 chr11:34255679-34255688
49	BCL11A	chr11:34256783-34257188	GM12878	blood:	n/a	n/a
50	BCL11A	chr11:34324010-34324466	GM12878	blood:	n/a	chr11:34324174-34324183 chr11:34324175-34324184

(count:794 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:34350440-34350490	AG09309	skin:	n/a
2	chr11:34350440-34350490	AG09309	skin:	n/a
3	chr11:34350440-34350490	HCF	heart:	n/a
4	chr11:34323678-34323728	MCF10A-Er-Src	breast:	n/a
5	chr11:34296462-34296512	HIPEpiC	eye:	n/a
6	chr11:34340108-34340158	PANC-1	pancreas:	n/a
7	chr11:34256703-34256753	T-47D	breast:	n/a
8	chr11:34288225-34288275	HIPEpiC	eye:	n/a
9	chr11:34265361-34265411	T-47D	breast:	n/a
10	chr11:34256703-34256753	AG04449	skin:	fetal
11	chr11:34265361-34265411	GM12891	blood:	n/a
12	chr11:34331908-34331958	HCPEpiC	choroid plexus:	n/a
13	chr11:34285529-34285579	Hepatocyte	liver:	n/a
14	chr11:34255733-34255783	LNCaP	prostate:	n/a
15	chr11:34331908-34331958	HEEpiC	esophagus:	n/a
16	chr11:34255733-34255783	SAEC	small airway:	n/a
17	chr11:34284610-34284660	HNPCEpiC	eye:	n/a
18	chr11:34296462-34296512	Hepatocyte	liver:	n/a
19	chr11:34296462-34296512	AG09319	gingival:	n/a
20	chr11:34256703-34256753	AG09319	gingival:	n/a
21	chr11:34285529-34285579	ovcar-3	ovarian:	n/a
22	chr11:34350440-34350490	SK-N-SH	brain:	n/a
23	chr11:34323678-34323728	HUVEC	blood vessel:	n/a
24	chr11:34273111-34273161	HMEC	breast:	n/a
25	chr11:34296462-34296512	HL-60	blood:	n/a
26	chr11:34285529-34285579	HL-60	blood:	n/a
27	chr11:34340108-34340158	HCM	heart:	n/a
28	chr11:34331908-34331958	SK-N-MC	brain:	n/a
29	chr11:34350440-34350490	ECC-1	luminal epithelium:	n/a
30	chr11:34340108-34340158	GM12892	blood:	n/a
31	chr11:34273111-34273161	SAEC	small airway:	n/a
32	chr11:34273111-34273161	A549	lung:	n/a
33	chr11:34255733-34255783	GM12892	blood:	n/a
34	chr11:34340108-34340158	HIPEpiC	eye:	n/a
35	chr11:34273111-34273161	T-47D	breast:	n/a
36	chr11:34288225-34288275	HCF	heart:	n/a
37	chr11:34296462-34296512	SK-N-SH_RA	brain:	n/a
38	chr11:34296462-34296512	GM19239	blood:	n/a
39	chr11:34288225-34288275	SK-N-SH_RA	brain:	n/a
40	chr11:34265361-34265411	CMK	blood:	n/a
41	chr11:34285529-34285579	MCF10A-Er-Src	breast:	n/a
42	chr11:34350440-34350490	HMEC	breast:	n/a
43	chr11:34350440-34350490	HPAEpiC	pulmonary alveolar:	n/a
44	chr11:34340108-34340158	SK-N-MC	brain:	n/a
45	chr11:34284610-34284660	NT2-D1	testis:	n/a
46	chr11:34340108-34340158	Hela-S3	cervix:	n/a
47	chr11:34288225-34288275	LNCaP	prostate:	n/a
48	chr11:34256703-34256753	RPTEC	kidney:	n/a
49	chr11:34256703-34256753	MCF-7	breast:	n/a
50	chr11:34323678-34323728	GM12878	blood:	n/a

(count:114 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr11:34127214..34128787-chr11:34317740..34319567,2	MCF-7	breast:
2	chr11:34317934..34320439-chr11:34320796..34323680,2	MCF-7	breast:
3	chr11:34328956..34331154-chr11:34336268..34338352,2	K562	blood:
4	chr11:34346331..34348538-chr11:34354788..34356481,2	MCF-7	breast:
5	chr11:34281972..34284178-chr11:34286435..34290431,3	K562	blood:
6	chr11:34256033..34257760-chr11:34260641..34262431,2	K562	blood:
7	chr11:34323353..34325328-chr11:34327561..34330383,2	MCF-7	breast:
8	chr11:34340006..34344767-chr11:34350658..34354959,5	MCF-7	breast:
9	chr11:34278605..34281312-chr11:34339472..34341100,2	K562	blood:
10	chr11:34317934..34320439-chr11:34320796..34323680,2	MCF-7	breast:
11	chr11:34306120..34306643-chr11:34317612..34318175,2	MCF-7	breast:
12	chr11:34352862..34355628-chr11:34375081..34377214,3	MCF-7	breast:
13	chr11:34285128..34287533-chr11:34298437..34301296,2	MCF-7	breast:
14	chr11:34345030..34348316-chr11:34348388..34351447,3	K562	blood:
15	chr11:34256033..34257760-chr11:34260641..34262431,2	K562	blood:
16	chr11:34283686..34286562-chr11:34377473..34379594,2	MCF-7	breast:
17	chr11:34268801..34271707-chr11:34290725..34293055,2	K562	blood:
18	chr11:34311842..34314169-chr11:34376736..34379276,3	MCF-7	breast:
19	chr11:34295781..34298473-chr11:34301568..34303802,2	MCF-7	breast:
20	chr11:34323353..34325328-chr11:34327561..34330383,2	MCF-7	breast:
21	chr11:34286604..34290357-chr11:34293722..34296590,3	MCF-7	breast:
22	chr11:34264193..34265705-chr11:34292865..34295828,2	K562	blood:
23	chr11:34267721..34270365-chr11:34272865..34274585,2	MCF-7	breast:
24	chr11:34270206..34274230-chr11:34378598..34380931,3	MCF-7	breast:
25	chr11:34306120..34306643-chr11:34317612..34318175,2	MCF-7	breast:
26	chr11:34309410..34312078-chr11:34318122..34319816,2	K562	blood:
27	chr11:34267721..34270365-chr11:34272865..34274585,2	MCF-7	breast:
28	chr11:34295048..34297358-chr11:34352691..34354542,2	MCF-7	breast:
29	chr11:34316702..34320022-chr11:34376124..34379659,5	MCF-7	breast:
30	chr11:34231932..34233684-chr11:34247435..34249545,2	K562	blood:
31	chr11:34295781..34298473-chr11:34301568..34303802,2	MCF-7	breast:
32	chr11:34297526..34299830-chr11:34304007..34305753,2	MCF-7	breast:
33	chr11:34269717..34273624-chr11:34376687..34380089,5	MCF-7	breast:
34	chr11:34301189..34303875-chr11:34378110..34380894,2	MCF-7	breast:
35	chr11:34295466..34297998-chr11:34348756..34350438,2	MCF-7	breast:
36	chr11:34295048..34297358-chr11:34352691..34354542,2	MCF-7	breast:
37	chr11:34263600..34266230-chr11:34266603..34268167,2	MCF-7	breast:
38	chr11:34330140..34331933-chr11:34345300..34347720,2	K562	blood:
39	chr11:34244635..34246968-chr11:34254314..34256180,3	K562	blood:
40	chr11:34345532..34347558-chr11:34378083..34380807,2	MCF-7	breast:
41	chr11:34306120..34306999-chr11:34317675..34318487,2	MCF-7	breast:
42	chr11:34355811..34357452-chr2:150425166..150428140,2	MCF-7	breast:
43	chr11:34306091..34307062-chr11:34317641..34318576,2	MCF-7	breast:
44	chr11:34295466..34297998-chr11:34348756..34350438,2	MCF-7	breast:
45	chr11:34276940..34279788-chr11:34309195..34311703,2	MCF-7	breast:
46	chr11:34348938..34354072-chr11:34377839..34381430,6	MCF-7	breast:
47	chr11:34229441..34231710-chr11:34255472..34258756,3	MCF-7	breast:
48	chr11:34260780..34263020-chr11:34279926..34282268,2	MCF-7	breast:
49	chr11:34264193..34265705-chr11:34292865..34295828,2	K562	blood:
50	chr11:34310476..34312267-chr11:34326192..34328969,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ELF5-4	chr11:34356665-34357550	NONHSAT018749

No data

Variant related genes	Relation type
ENSG00000254708	TF binding region
ABTB2	TF binding region
ENSG00000254708	CpG island
ABTB2	CpG island
ENSG00000254708	chromatin interactions
ENSG00000135372	chromatin interactions
ENSG00000166016	chromatin interactions

Extended variants
information (count: 4408 )
Associated
traits (count: 80 )

Variant overlapped rSNPs/rCNVs (count:4408 , 50 per page) page: 1 2 3 4 5 6 7 ... 89

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2473900	chr11:34247462-34247463	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs180735602	chr11:34247480-34247481	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs574057685	chr11:34247489-34247490	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs377356046	chr11:34247516-34247517	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs535588121	chr11:34247522-34247523	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs555318797	chr11:34247579-34247580	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs575481051	chr11:34247583-34247584	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs143595896	chr11:34247657-34247658	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs571373331	chr11:34247751-34247752	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs558108855	chr11:34247772-34247773	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs34915007	chr11:34247774-34247775	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs72912578	chr11:34247775-34247776	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs4756117	chr11:34247814-34247815	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs147196135	chr11:34247823-34247824	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs560147682	chr11:34247883-34247884	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs74388693	chr11:34247909-34247910	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs140590098	chr11:34247922-34247923	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs562972856	chr11:34248034-34248035	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs536483307	chr11:34248047-34248048	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs184508299	chr11:34248082-34248083	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs76546632	chr11:34248147-34248148	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs571622536	chr11:34248158-34248159	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs4755363	chr11:34248229-34248230	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
24	rs547476016	chr11:34248325-34248326	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs200056906	chr11:34248378-34248379	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs536383168	chr11:34248478-34248479	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs289983	chr11:34248540-34248541	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs289984	chr11:34248566-34248567	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs538057273	chr11:34248584-34248585	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs6484701	chr11:34248586-34248587	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs578001418	chr11:34248590-34248591	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs7118745	chr11:34248619-34248620	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs553528985	chr11:34248624-34248625	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs543901575	chr11:34248641-34248642	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs9783356	chr11:34248689-34248690	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs575733426	chr11:34248690-34248691	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs370637530	chr11:34248724-34248725	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs542384607	chr11:34248748-34248749	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs562624574	chr11:34248756-34248757	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs189317345	chr11:34248802-34248803	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs372284660	chr11:34248820-34248821	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs372031668	chr11:34248833-34248834	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs200772478	chr11:34248834-34248835	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs74739876	chr11:34248846-34248847	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs371366218	chr11:34248848-34248849	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs374993462	chr11:34248903-34248904	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs139672252	chr11:34248936-34248937	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs73493563	chr11:34248941-34248942	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs146807995	chr11:34248949-34248950	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs167054	chr11:34249011-34249012	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

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
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Cancer	20164919	CNVD

Chromatin state (count:2852 , 50 per page) page: 1 2 3 4 5 6 7 ... 58

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:34237200-34255600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
2	chr11:34245200-34254600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
3	chr11:34245200-34255400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr11:34245200-34255600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr11:34245200-34255800	Weak transcription	HSMMtube	muscle
6	chr11:34245200-34263800	Weak transcription	Right Atrium	heart
7	chr11:34245200-34264200	Weak transcription	Aorta	Aorta
8	chr11:34245400-34251400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
9	chr11:34245400-34254600	Weak transcription	HUES6 Cell Line	embryonic stem cell
10	chr11:34245400-34255600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
11	chr11:34245400-34255600	Weak transcription	NHLF	lung
12	chr11:34245600-34263600	Weak transcription	Right Ventricle	heart
13	chr11:34246000-34247800	Weak transcription	Rectal Mucosa Donor 29	rectum
14	chr11:34246200-34247800	Weak transcription	Sigmoid Colon	Sigmoid Colon
15	chr11:34246200-34255600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr11:34246800-34247800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
17	chr11:34246800-34255800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
18	chr11:34247000-34248000	Weak transcription	Duodenum Mucosa	Duodenum
19	chr11:34247000-34254800	Weak transcription	Fetal Intestine Small	intestine
20	chr11:34247000-34255800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
21	chr11:34247000-34257400	Weak transcription	Fetal Stomach	stomach
22	chr11:34247200-34247600	Weak transcription	Rectal Mucosa Donor 31	rectum
23	chr11:34247600-34248200	Enhancers	Rectal Mucosa Donor 31	rectum
24	chr11:34247800-34248000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
25	chr11:34247800-34248000	Enhancers	Colon Smooth Muscle	Colon
26	chr11:34247800-34248200	Enhancers	Primary monocytes fromperipheralblood	blood
27	chr11:34247800-34248200	Enhancers	Primary hematopoietic stem cells short term culture	blood
28	chr11:34247800-34248200	Enhancers	Sigmoid Colon	Sigmoid Colon
29	chr11:34247800-34248200	Enhancers	Monocytes-CD14+_RO01746	blood
30	chr11:34247800-34248400	Enhancers	Rectal Mucosa Donor 29	rectum
31	chr11:34248000-34248200	Enhancers	Duodenum Mucosa	Duodenum
32	chr11:34248000-34248200	Enhancers	Placenta Amnion	Placenta Amnion
33	chr11:34248000-34248200	Enhancers	GM12878-XiMat	blood
34	chr11:34248200-34249400	Weak transcription	Duodenum Mucosa	Duodenum
35	chr11:34248200-34251600	Weak transcription	GM12878-XiMat	blood
36	chr11:34248200-34254600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
37	chr11:34249600-34263600	Weak transcription	Gastric	stomach
38	chr11:34251600-34252000	Enhancers	ES-I3 Cell Line	embryonic stem cell
39	chr11:34251600-34252000	Enhancers	iPS-15b Cell Line	embryonic stem cell
40	chr11:34251600-34255400	Enhancers	GM12878-XiMat	blood
41	chr11:34251800-34255400	Weak transcription	H1 Cell Line	embryonic stem cell
42	chr11:34251800-34255600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
43	chr11:34252000-34255400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
44	chr11:34252000-34255600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
45	chr11:34252600-34253800	Enhancers	A549	lung
46	chr11:34252800-34253200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
47	chr11:34253200-34253600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
48	chr11:34253600-34256000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
49	chr11:34253800-34254600	Weak transcription	A549	lung
50	chr11:34254000-34256400	Enhancers	Primary B cells from peripheral blood	blood

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