Variant report

Variant	esv1798271
Chromosome Location	chr11:94144987-94227993
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1163)
CpG islands
(count:1344)
Chromatin interactive
region (count:72)
LncRNA
region (count:2)
Mature miRNA
region (count: 1)
miRNA target
sites (count:1)

(count:1163 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:94226621-94227809	HepG2	liver:	n/a	n/a
2	ARID3A	chr11:94182551-94182968	HepG2	liver:	n/a	n/a
3	ARID3A	chr11:94226313-94226540	K562	blood:	n/a	n/a
4	ARID3A	chr11:94190158-94190455	K562	blood:	n/a	n/a
5	ARID3A	chr11:94226817-94227053	K562	blood:	n/a	n/a
6	ARID3A	chr11:94159572-94159575	K562	blood:	n/a	n/a
7	ATF1	chr11:94226839-94227255	K562	blood:	n/a	n/a
8	ATF1	chr11:94202722-94202923	K562	blood:	n/a	n/a
9	ATF2	chr11:94206409-94207070	GM12878	blood:	n/a	n/a
10	ATF2	chr11:94226652-94227512	GM12878	blood:	n/a	n/a
11	ATF2	chr11:94227299-94227715	H1-hESC	embryonic stem cell:	n/a	n/a
12	ATF2	chr11:94192705-94193059	GM12878	blood:	n/a	n/a
13	ATF2	chr11:94190859-94191286	GM12878	blood:	n/a	n/a
14	ATF2	chr11:94202437-94203093	GM12878	blood:	n/a	n/a
15	ATF2	chr11:94226375-94227236	H1-hESC	embryonic stem cell:	n/a	n/a
16	ATF2	chr11:94190887-94191278	GM12878	blood:	n/a	n/a
17	ATF2	chr11:94206315-94207163	GM12878	blood:	n/a	n/a
18	ATF2	chr11:94202590-94203078	GM12878	blood:	n/a	n/a
19	ATF2	chr11:94226438-94227189	H1-hESC	embryonic stem cell:	n/a	n/a
20	ATF2	chr11:94226566-94227214	GM12878	blood:	n/a	n/a
21	ATF2	chr11:94192680-94193125	GM12878	blood:	n/a	n/a
22	ATF3	chr11:94190901-94191198	K562	blood:	n/a	n/a
23	ATF3	chr11:94189034-94189433	HCT-116	colon:	n/a	n/a
24	BACH1	chr11:94190380-94190664	K562	blood:	n/a	n/a
25	BACH1	chr11:94226529-94227423	H1-hESC	embryonic stem cell:	n/a	n/a
26	BATF	chr11:94192706-94193076	GM12878	blood:	n/a	n/a
27	BATF	chr11:94206462-94206951	GM12878	blood:	n/a	n/a
28	BATF	chr11:94192692-94193101	GM12878	blood:	n/a	n/a
29	BATF	chr11:94202619-94202935	GM12878	blood:	n/a	n/a
30	BATF	chr11:94190861-94191247	GM12878	blood:	n/a	n/a
31	BATF	chr11:94206447-94206972	GM12878	blood:	n/a	n/a
32	BATF	chr11:94202501-94202988	GM12878	blood:	n/a	n/a
33	BCL11A	chr11:94206606-94206926	GM12878	blood:	n/a	n/a
34	BCL11A	chr11:94202633-94202934	GM12878	blood:	n/a	n/a
35	BCL11A	chr11:94202628-94202903	GM12878	blood:	n/a	n/a
36	BCL11A	chr11:94192717-94193037	GM12878	blood:	n/a	n/a
37	BCL11A	chr11:94206571-94206984	GM12878	blood:	n/a	n/a
38	BCL3	chr11:94182483-94183043	A549	lung:	n/a	n/a
39	BCL3	chr11:94206427-94206992	GM12878	blood:	n/a	n/a
40	BCLAF1	chr11:94206462-94206978	GM12878	blood:	n/a	n/a
41	BCLAF1	chr11:94190851-94191212	GM12878	blood:	n/a	n/a
42	BCLAF1	chr11:94206455-94207001	GM12878	blood:	n/a	n/a
43	BHLHE40	chr11:94226945-94227545	GM12878	blood:	n/a	n/a
44	BHLHE40	chr11:94206435-94206990	GM12878	blood:	n/a	n/a
45	BHLHE40	chr11:94192797-94193020	GM12878	blood:	n/a	n/a
46	BHLHE40	chr11:94182618-94182907	HepG2	liver:	n/a	n/a
47	BHLHE40	chr11:94202204-94203137	GM12878	blood:	n/a	n/a
48	BHLHE40	chr11:94226647-94227663	K562	blood:	n/a	n/a
49	BHLHE40	chr11:94186624-94186760	GM12878	blood:	n/a	n/a
50	BRCA1	chr11:94226782-94227267	HepG2	liver:	n/a	chr11:94227016-94227025

(count:1344 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:94227081-94227131	AG09319	gingival:	n/a
2	chr11:94227583-94227633	SAEC	small airway:	n/a
3	chr11:94227081-94227131	AG09319	gingival:	n/a
4	chr11:94227583-94227633	SAEC	small airway:	n/a
5	chr11:94207287-94207337	HAEpiC	amniotic membrane:	n/a
6	chr11:94227038-94227088	HL-60	blood:	n/a
7	chr11:94227320-94227370	HEEpiC	esophagus:	n/a
8	chr11:94224044-94224094	MCF10A-Er-Src	breast:	n/a
9	chr11:94227006-94227056	NH-A	brain:	n/a
10	chr11:94226925-94226975	HNPCEpiC	eye:	n/a
11	chr11:94227109-94227159	A549	lung:	n/a
12	chr11:94224044-94224094	HCPEpiC	choroid plexus:	n/a
13	chr11:94227411-94227461	AG04449	skin:	fetal
14	chr11:94224044-94224094	AG04450	lung:	fetal
15	chr11:94227183-94227233	NH-A	brain:	n/a
16	chr11:94227081-94227131	MCF-7	breast:	n/a
17	chr11:94145963-94146013	HRPEpiC	eye:	n/a
18	chr11:94226767-94226817	H1-hESC	embryonic stem cell:	embryo
19	chr11:94150725-94150775	AoSMC	blood vessel:	n/a
20	chr11:94227038-94227088	GM06990	blood:	n/a
21	chr11:94166952-94167002	HL-60	blood:	n/a
22	chr11:94207287-94207337	Hepatocyte	liver:	n/a
23	chr11:94226991-94227041	HCM	heart:	n/a
24	chr11:94172892-94172942	AG04450	lung:	fetal
25	chr11:94227081-94227131	LNCaP	prostate:	n/a
26	chr11:94224044-94224094	SK-N-SH_RA	brain:	n/a
27	chr11:94227380-94227430	MCF10A-Er-Src	breast:	n/a
28	chr11:94226925-94226975	IMR90	lung:	fetal
29	chr11:94227038-94227088	SKMC	muscle:	n/a
30	chr11:94227006-94227056	Caco-2	colon:	n/a
31	chr11:94207287-94207337	SK-N-MC	brain:	n/a
32	chr11:94226925-94226975	HAEpiC	amniotic membrane:	n/a
33	chr11:94227081-94227131	HCF	heart:	n/a
34	chr11:94150725-94150775	A549	lung:	n/a
35	chr11:94227320-94227370	K562	blood:	n/a
36	chr11:94166952-94167002	NHBE	bronchial:	n/a
37	chr11:94227380-94227430	MCF-7	breast:	n/a
38	chr11:94227183-94227233	HMEC	breast:	n/a
39	chr11:94226991-94227041	HRCEpiC	kidney:	n/a
40	chr11:94172892-94172942	HCPEpiC	choroid plexus:	n/a
41	chr11:94226537-94226587	NT2-D1	testis:	n/a
42	chr11:94227109-94227159	HEEpiC	esophagus:	n/a
43	chr11:94227006-94227056	Hepatocyte	liver:	n/a
44	chr11:94227125-94227175	GM06990	blood:	n/a
45	chr11:94224044-94224094	PFSK-1	brain:	n/a
46	chr11:94227125-94227175	NT2-D1	testis:	n/a
47	chr11:94207287-94207337	NT2-D1	testis:	n/a
48	chr11:94227006-94227056	AG04449	skin:	fetal
49	chr11:94227109-94227159	K562	blood:	n/a
50	chr11:94224044-94224094	Hela-S3	cervix:	n/a

(count:72 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr11:94143610..94146567-chr11:94146624..94148573,2	K562	blood:
2	chr11:94200661..94202892-chr11:94224214..94225865,2	K562	blood:
3	chr11:94202207..94203763-chr11:94208218..94210423,2	K562	blood:
4	chr11:94226287..94227152-chr12:49524847..49525416,2	Hela-S3	cervix:
5	chr11:94151626..94153419-chr11:94155927..94158311,2	K562	blood:
6	chr11:93914625..93916953-chr11:94227203..94228744,2	MCF-7	breast:
7	chr11:94226771..94229140-chr11:94275887..94279295,4	K562	blood:
8	chr11:94213539..94215601-chr11:94228089..94230235,2	K562	blood:
9	chr11:94202207..94203763-chr11:94208218..94210423,2	K562	blood:
10	chr11:94209182..94211578-chr11:94214221..94216536,2	K562	blood:
11	chr11:94210098..94212202-chr11:94216700..94218600,2	K562	blood:
12	chr11:94226544..94227246-chr17:33904994..33905713,2	Hela-S3	cervix:
13	chr11:94143104..94144864-chr11:94174471..94176853,2	K562	blood:
14	chr11:94210078..94211620-chr11:94214056..94215721,2	K562	blood:
15	chr11:93916648..93917265-chr11:94150276..94150816,3	MCF-7	breast:
16	chr11:94209182..94211578-chr11:94214221..94216536,2	K562	blood:
17	chr11:94217659..94221782-chr11:94225032..94227665,4	K562	blood:
18	chr11:94217826..94221118-chr11:94222264..94225071,4	K562	blood:
19	chr11:94147038..94148979-chr11:94159027..94161270,2	K562	blood:
20	chr11:94058553..94059494-chr11:94150256..94151536,4	MCF-7	breast:
21	chr11:94089973..94092679-chr11:94143907..94145994,2	K562	blood:
22	chr11:94187673..94189503-chr11:94190154..94193053,2	K562	blood:
23	chr11:94185882..94188334-chr11:94225104..94227120,2	K562	blood:
24	chr11:94226137..94228706-chr11:94300541..94302920,2	K562	blood:
25	chr11:94170626..94172978-chr11:94174814..94177499,3	K562	blood:
26	chr11:94213449..94216550-chr11:94217098..94220299,3	K562	blood:
27	chr11:94187673..94189503-chr11:94190154..94193053,2	K562	blood:
28	chr11:94040991..94041600-chr11:94150266..94151213,2	MCF-7	breast:
29	chr11:94208946..94211928-chr11:94232056..94233967,2	MCF-7	breast:
30	chr11:94226700..94227357-chr19:7293430..7294141,2	Hela-S3	cervix:
31	chr11:94213347..94215361-chr11:94222222..94224695,2	K562	blood:
32	chr11:94144560..94146468-chr11:94146702..94148418,2	MCF-7	breast:
33	chr11:94217826..94221118-chr11:94222264..94225071,4	K562	blood:
34	chr11:94210098..94212202-chr11:94216700..94218600,2	K562	blood:
35	chr11:93916755..93917614-chr11:94150312..94151338,4	MCF-7	breast:
36	chr11:94180184..94182302-chr11:94227182..94229296,2	K562	blood:
37	chr11:94151210..94154099-chr11:94225020..94227256,2	MCF-7	breast:
38	chr11:94143610..94146567-chr11:94146624..94148573,2	K562	blood:
39	chr11:94225466..94228271-chr11:94275709..94278301,3	K562	blood:
40	chr11:94198479..94200826-chr11:94200987..94202578,2	K562	blood:
41	chr11:94208132..94210778-chr19:13263700..13265621,2	K562	blood:
42	chr11:94146817..94148995-chr11:94151146..94153752,2	K562	blood:
43	chr11:93472910..93474648-chr11:94197238..94199366,2	MCF-7	breast:
44	chr11:94219618..94222085-chr11:94222930..94224543,2	K562	blood:
45	chr11:94151626..94153419-chr11:94155927..94158311,2	K562	blood:
46	chr11:94225979..94229384-chr11:94230397..94235421,9	K562	blood:
47	chr11:94213347..94215361-chr11:94222222..94224695,2	K562	blood:
48	chr11:94219714..94224180-chr11:94224527..94226991,4	MCF-7	breast:
49	chr11:94210078..94211620-chr11:94214056..94215721,2	K562	blood:
50	chr11:94170626..94172978-chr11:94174814..94177499,3	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GPR83-1	chr11:94206074-94206627	ENSG00000255893.1
2	lnc-GPR83-1	chr11:94206710-94206736	ENSG00000255893.1

miRNA name	Chromosome Location	mirBase accession
hsa-miR-548l	chr11:94199711-94199732	MIMAT0005889

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	MRE11A	hsa-miR-373-3p	chr11:94152021-94152040

Variant related genes	Relation type
ENSG00000255893	TF binding region
ANKRD49	TF binding region
ENSG00000263966	TF binding region
MRE11A	TF binding region
MIR548L	TF binding region
ENSG00000255893	CpG island
ANKRD49	CpG island
ENSG00000263966	CpG island
MRE11A	CpG island
MIR548L	CpG island
ENSG00000108733	chromatin interactions
ENSG00000182919	chromatin interactions
ENSG00000166012	chromatin interactions
ENSG00000258017	chromatin interactions
ENSG00000134627	chromatin interactions
ENSG00000267598	chromatin interactions
ENSG00000196371	chromatin interactions
ENSG00000020922	chromatin interactions
ENSG00000171105	chromatin interactions
ENSG00000168876	chromatin interactions
ENSG00000221230	chromatin interactions
ENSG00000255893	chromatin interactions
ENSG00000123416	chromatin interactions
ENSG00000006125	chromatin interactions
ENSG00000110218	chromatin interactions

Extended variants
information (count: 3206 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:3206 , 50 per page) page: 1 2 3 4 5 6 7 ... 65

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs584531	chr11:94144987-94144988	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs547470506	chr11:94145002-94145003	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs535492701	chr11:94145011-94145012	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs567449638	chr11:94145013-94145014	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs150278683	chr11:94145014-94145015	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs79850307	chr11:94145025-94145026	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	mRNA abundance
7	rs528003922	chr11:94145123-94145124	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs546022892	chr11:94145131-94145132	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs146885397	chr11:94145163-94145164	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs576649204	chr11:94145182-94145183	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs370474286	chr11:94145183-94145184	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs543763976	chr11:94145199-94145200	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs373488980	chr11:94145209-94145210	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs376528972	chr11:94145230-94145231	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs181423460	chr11:94145253-94145254	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs370356397	chr11:94145367-94145368	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs140699085	chr11:94145378-94145379	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs527464896	chr11:94145389-94145390	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs185770222	chr11:94145406-94145407	Bivalent/Poised TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs10831224	chr11:94145480-94145481	Bivalent/Poised TSS Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs11601086	chr11:94145518-94145519	Bivalent/Poised TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs549815602	chr11:94145544-94145545	Bivalent/Poised TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs145810302	chr11:94145551-94145552	Bivalent/Poised TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs535133915	chr11:94145592-94145593	Bivalent/Poised TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs553436085	chr11:94145636-94145637	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs565403742	chr11:94145678-94145679	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs539170769	chr11:94145683-94145684	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs557886171	chr11:94145726-94145727	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs138376583	chr11:94145727-94145728	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs189742875	chr11:94145730-94145731	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs555829729	chr11:94145747-94145748	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs180906299	chr11:94145749-94145750	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs541469359	chr11:94145772-94145773	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs375648997	chr11:94145783-94145784	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs578122915	chr11:94145814-94145815	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs376626179	chr11:94145830-94145831	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs186401190	chr11:94145836-94145837	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs201585068	chr11:94145855-94145856	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs11350529	chr11:94145862-94145863	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs397775544	chr11:94145879-94145880	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs539322890	chr11:94145904-94145905	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs564265165	chr11:94145907-94145908	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs534826466	chr11:94145938-94145939	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs559341231	chr11:94145951-94145952	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs572669641	chr11:94145953-94145954	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs114312575	chr11:94145964-94145965	Weak transcription Strong transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a
47	rs199910822	chr11:94146045-94146046	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs149601389	chr11:94146053-94146054	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs143285651	chr11:94146062-94146063	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs557533494	chr11:94146065-94146066	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:81)

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
Non-syndromic sensorineural hearing loss	18451855	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:2548 , 50 per page) page: 1 2 3 4 5 6 7 ... 51

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:94135200-94161400	Weak transcription	Placenta	Placenta
2	chr11:94135200-94162200	Weak transcription	Brain Inferior Temporal Lobe	brain
3	chr11:94138600-94162200	Weak transcription	Brain Cingulate Gyrus	brain
4	chr11:94141200-94155000	Weak transcription	Primary T cells from cord blood	blood
5	chr11:94141800-94156600	Weak transcription	Spleen	Spleen
6	chr11:94142000-94154800	Weak transcription	Primary hematopoietic stem cells	blood
7	chr11:94142400-94161200	Weak transcription	Brain Anterior Caudate	brain
8	chr11:94142600-94154800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr11:94142800-94152200	Weak transcription	Liver	Liver
10	chr11:94142800-94156000	Weak transcription	Thymus	Thymus
11	chr11:94143000-94150400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
12	chr11:94143200-94156400	Weak transcription	Fetal Stomach	stomach
13	chr11:94143400-94145800	Weak transcription	Dnd41	blood
14	chr11:94143400-94156400	Weak transcription	Gastric	stomach
15	chr11:94143600-94147400	Weak transcription	Monocytes-CD14+_RO01746	blood
16	chr11:94143600-94154800	Weak transcription	Fetal Muscle Trunk	muscle
17	chr11:94143600-94156400	Weak transcription	Lung	lung
18	chr11:94143800-94148600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
19	chr11:94143800-94151600	Weak transcription	Primary T cells fromperipheralblood	blood
20	chr11:94143800-94156200	Weak transcription	Fetal Intestine Small	intestine
21	chr11:94143800-94156400	Weak transcription	Ovary	ovary
22	chr11:94144000-94147400	Weak transcription	Primary monocytes fromperipheralblood	blood
23	chr11:94144200-94169200	Weak transcription	Aorta	Aorta
24	chr11:94144400-94153600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr11:94145000-94145200	Enhancers	HUES48 Cell Line	embryonic stem cell
26	chr11:94145000-94156400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
27	chr11:94145000-94161800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
28	chr11:94145200-94145400	Enhancers	iPS-18 Cell Line	embryonic stem cell
29	chr11:94145200-94145400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
30	chr11:94145200-94152800	Weak transcription	HUES48 Cell Line	embryonic stem cell
31	chr11:94145400-94145600	Bivalent/Poised TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr11:94145400-94154800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
33	chr11:94145400-94162000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
34	chr11:94145600-94147200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr11:94145800-94146600	Strong transcription	Dnd41	blood
36	chr11:94146200-94148200	Weak transcription	Duodenum Smooth Muscle	Duodenum
37	chr11:94146200-94156400	Weak transcription	Duodenum Mucosa	Duodenum
38	chr11:94146400-94148200	Weak transcription	Adipose Nuclei	Adipose
39	chr11:94146400-94148400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
40	chr11:94146400-94148400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chr11:94146400-94148600	Weak transcription	Primary B cells from cord blood	blood
42	chr11:94146400-94161200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
43	chr11:94146600-94148200	Weak transcription	Dnd41	blood
44	chr11:94146600-94148600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
45	chr11:94146600-94148600	Weak transcription	Primary neutrophils fromperipheralblood	blood
46	chr11:94146600-94152000	Weak transcription	A549	lung
47	chr11:94146600-94153200	Weak transcription	HUES6 Cell Line	embryonic stem cell
48	chr11:94146600-94154800	Weak transcription	Fetal Thymus	thymus
49	chr11:94146800-94148600	Weak transcription	Fetal Brain Female	brain
50	chr11:94146800-94156400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--

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