Variant report

Variant	nsv541025
Chromosome Location	chr11:45154352-45193352
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:749)
CpG islands
(count:671)
Chromatin interactive
region (count:58)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:749 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:45167670-45167842	HepG2	liver:	n/a	n/a
2	ARID3A	chr11:45168717-45169083	HepG2	liver:	n/a	n/a
3	ATF1	chr11:45168645-45168977	K562	blood:	n/a	n/a
4	ATF2	chr11:45162731-45163058	GM12878	blood:	n/a	n/a
5	ATF3	chr11:45168339-45168512	K562	blood:	n/a	n/a
6	ATF3	chr11:45168695-45168861	K562	blood:	n/a	chr11:45168842-45168851
7	ATF3	chr11:45168614-45168859	K562	blood:	n/a	chr11:45168842-45168851
8	BACH1	chr11:45168731-45169234	H1-hESC	embryonic stem cell:	n/a	n/a
9	BATF	chr11:45162802-45163034	GM12878	blood:	n/a	n/a
10	BCLAF1	chr11:45168582-45168978	GM12878	blood:	n/a	chr11:45168879-45168892 chr11:45168876-45168889 chr11:45168878-45168891 chr11:45168926-45168939
11	BHLHE40	chr11:45168744-45168826	K562	blood:	n/a	n/a
12	BHLHE40	chr11:45167451-45167526	K562	blood:	n/a	n/a
13	BHLHE40	chr11:45168651-45168966	GM12878	blood:	n/a	chr11:45168921-45168937 chr11:45168918-45168934 chr11:45168915-45168931
14	BHLHE40	chr11:45178425-45178763	HepG2	liver:	n/a	n/a
15	BRCA1	chr11:45168734-45169265	HepG2	liver:	n/a	n/a
16	BRCA1	chr11:45168649-45169275	Hela-S3	cervix:	n/a	n/a
17	BRCA1	chr11:45167471-45168136	Hela-S3	cervix:	n/a	n/a
18	CBX3	chr11:45168605-45168942	K562	blood:	n/a	n/a
19	CCNT2	chr11:45168019-45169060	K562	blood:	n/a	n/a
20	CEBPB	chr11:45168084-45169567	Hela-S3	cervix:	n/a	n/a
21	CEBPB	chr11:45167137-45167436	HepG2	liver:	n/a	n/a
22	CEBPB	chr11:45157885-45158159	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr11:45167142-45167377	H1-hESC	embryonic stem cell:	n/a	n/a
24	CEBPB	chr11:45158029-45158071	H1-hESC	embryonic stem cell:	n/a	n/a
25	CEBPB	chr11:45189952-45190003	HepG2	liver:	n/a	chr11:45189989-45190000 chr11:45189987-45189998
26	CEBPB	chr11:45177978-45178322	MCF-7	breast:	n/a	n/a
27	CEBPB	chr11:45177954-45178251	MCF-7	breast:	n/a	n/a
28	CEBPD	chr11:45168584-45168994	HepG2	liver:	n/a	n/a
29	CEBPD	chr11:45168000-45168259	HepG2	liver:	n/a	n/a
30	CHD1	chr11:45167584-45168292	H1-hESC	embryonic stem cell:	n/a	n/a
31	CHD1	chr11:45168678-45168892	GM12878	blood:	n/a	chr11:45168843-45168853
32	CHD2	chr11:45168613-45169191	GM12878	blood:	n/a	chr11:45168843-45168853
33	CHD2	chr11:45167121-45167431	H1-hESC	embryonic stem cell:	n/a	n/a
34	CHD2	chr11:45168631-45169064	K562	blood:	n/a	chr11:45168843-45168853
35	CHD2	chr11:45190432-45190551	H1-hESC	embryonic stem cell:	n/a	n/a
36	CHD2	chr11:45168266-45168273	K562	blood:	n/a	n/a
37	CHD2	chr11:45168635-45169095	HepG2	liver:	n/a	chr11:45168843-45168853
38	CHD2	chr11:45167681-45169502	Hela-S3	cervix:	n/a	chr11:45168843-45168853
39	CHD2	chr11:45168599-45169203	H1-hESC	embryonic stem cell:	n/a	chr11:45168843-45168853
40	CREB1	chr11:45168557-45169269	H1-hESC	embryonic stem cell:	n/a	n/a
41	CREB1	chr11:45168485-45169102	GM12878	blood:	n/a	n/a
42	CREB1	chr11:45168629-45168951	ECC-1	luminal epithelium:	n/a	n/a
43	CREB1	chr11:45167955-45168523	A549	lung:	n/a	n/a
44	CREB1	chr11:45162795-45163119	GM12878	blood:	n/a	n/a
45	CREB1	chr11:45168588-45169173	H1-hESC	embryonic stem cell:	n/a	n/a
46	CREB1	chr11:45168566-45169203	A549	lung:	n/a	n/a
47	CREB1	chr11:45168608-45169050	K562	blood:	n/a	n/a
48	CREB1	chr11:45168617-45169113	K562	blood:	n/a	n/a
49	CREB1	chr11:45168594-45169177	HepG2	liver:	n/a	n/a
50	CREB1	chr11:45168618-45168947	A549	lung:	n/a	n/a

(count:671 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:45167368-45167418	SK-N-SH_RA	brain:	n/a
2	chr11:45168563-45168613	GM12892	blood:	n/a
3	chr11:45169082-45169132	U87	brain:	n/a
4	chr11:45167702-45167752	HCM	heart:	n/a
5	chr11:45171428-45171478	HRE	kidney:	n/a
6	chr11:45167419-45167469	AG09319	gingival:	n/a
7	chr11:45179364-45179414	NT2-D1	testis:	n/a
8	chr11:45179364-45179414	MCF10A-Er-Src	breast:	n/a
9	chr11:45171428-45171478	SKMC	muscle:	n/a
10	chr11:45167805-45167855	MCF-7	breast:	n/a
11	chr11:45169082-45169132	NB4	blood:	n/a
12	chr11:45167493-45167543	PFSK-1	brain:	n/a
13	chr11:45167419-45167469	SKMC	muscle:	n/a
14	chr11:45168563-45168613	GM19239	blood:	n/a
15	chr11:45166384-45166434	HRE	kidney:	n/a
16	chr11:45167419-45167469	HMEC	breast:	n/a
17	chr11:45179364-45179414	AG09319	gingival:	n/a
18	chr11:45167805-45167855	HRPEpiC	eye:	n/a
19	chr11:45167419-45167469	HNPCEpiC	eye:	n/a
20	chr11:45166384-45166434	NHDF-neo	bronchial:	n/a
21	chr11:45171428-45171478	AG10803	skin:	n/a
22	chr11:45179364-45179414	SK-N-MC	brain:	n/a
23	chr11:45168563-45168613	T-47D	breast:	n/a
24	chr11:45171428-45171478	HIPEpiC	eye:	n/a
25	chr11:45168563-45168613	AoSMC	blood vessel:	n/a
26	chr11:45168563-45168613	HCF	heart:	n/a
27	chr11:45168563-45168613	SKMC	muscle:	n/a
28	chr11:45179364-45179414	HEK293	kidney:	embryo
29	chr11:45167493-45167543	IMR90	lung:	fetal
30	chr11:45171428-45171478	AG04449	skin:	fetal
31	chr11:45168563-45168613	Hepatocyte	liver:	n/a
32	chr11:45167368-45167418	PrEC	prostate:	n/a
33	chr11:45167419-45167469	HCF	heart:	n/a
34	chr11:45167368-45167418	HMEC	breast:	n/a
35	chr11:45179364-45179414	NHBE	bronchial:	n/a
36	chr11:45167772-45167822	HCT-116	colon:	n/a
37	chr11:45167493-45167543	K562	blood:	n/a
38	chr11:45179364-45179414	AoSMC	blood vessel:	n/a
39	chr11:45169082-45169132	NHBE	bronchial:	n/a
40	chr11:45169082-45169132	HCPEpiC	choroid plexus:	n/a
41	chr11:45167805-45167855	ovcar-3	ovarian:	n/a
42	chr11:45167493-45167543	ovcar-3	ovarian:	n/a
43	chr11:45166384-45166434	PANC-1	pancreas:	n/a
44	chr11:45167702-45167752	K562	blood:	n/a
45	chr11:45169082-45169132	A549	lung:	n/a
46	chr11:45169082-45169132	IMR90	lung:	fetal
47	chr11:45168563-45168613	HRCEpiC	kidney:	n/a
48	chr11:45166384-45166434	SAEC	small airway:	n/a
49	chr11:45167368-45167418	NB4	blood:	n/a
50	chr11:45167702-45167752	PFSK-1	brain:	n/a

(count:58 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr11:45167893..45171206-chr11:45200303..45204446,5	MCF-7	breast:
2	chr11:45167897..45170381-chr11:45182910..45186280,3	MCF-7	breast:
3	chr11:45178718..45181474-chr11:45186088..45187942,2	K562	blood:
4	chr11:45192972..45194599-chr11:45201172..45203381,2	MCF-7	breast:
5	chr11:45178718..45181474-chr11:45186088..45187942,2	K562	blood:
6	chr11:45155054..45156801-chr11:45201553..45203691,2	MCF-7	breast:
7	chr11:45176699..45178353-chr11:45180660..45182490,2	K562	blood:
8	chr11:45184515..45187339-chr11:45200209..45203185,3	MCF-7	breast:
9	chr11:45165135..45167115-chr11:45369738..45371244,2	MCF-7	breast:
10	chr11:45155937..45158191-chr11:45167233..45169516,2	MCF-7	breast:
11	chr11:45166948..45170773-chr11:45176737..45181280,4	K562	blood:
12	chr11:45175178..45177497-chr11:45190478..45192901,2	MCF-7	breast:
13	chr11:45155420..45158264-chr11:45165357..45168555,3	K562	blood:
14	chr11:45168231..45168959-chr2:96810761..96811512,2	Hela-S3	cervix:
15	chr11:45168840..45171324-chr11:45179427..45182574,4	K562	blood:
16	chr11:45175178..45177497-chr11:45190478..45192901,2	MCF-7	breast:
17	chr1:228352747..228353404-chr11:45167742..45168503,2	Hela-S3	cervix:
18	chr11:45188977..45190924-chr17:57920885..57923091,2	MCF-7	breast:
19	chr11:45167324..45169317-chr11:45187434..45189028,2	MCF-7	breast:
20	chr11:45154187..45156497-chr11:45867707..45870447,2	MCF-7	breast:
21	chr11:45156473..45158186-chr11:45161374..45164148,2	K562	blood:
22	chr11:45184640..45186467-chr11:45245800..45248700,2	MCF-7	breast:
23	chr11:45155420..45158264-chr11:45164649..45168555,5	K562	blood:
24	chr11:45175116..45179672-chr11:45200428..45203177,5	MCF-7	breast:
25	chr11:45173226..45176543-chr11:45176880..45179156,4	K562	blood:
26	chr11:45167645..45169641-chr11:45170241..45173572,4	K562	blood:
27	chr11:45176125..45178660-chr11:45202397..45204482,2	MCF-7	breast:
28	chr11:45167440..45169930-chr11:45202656..45204248,2	K562	blood:
29	chr11:45141259..45143495-chr11:45154866..45157797,2	MCF-7	breast:
30	chr11:45167789..45170487-chr11:45182645..45184245,2	K562	blood:
31	chr11:44940135..44943122-chr11:45165602..45168415,2	MCF-7	breast:
32	chr11:45164428..45170441-chr11:45176063..45179885,12	MCF-7	breast:
33	chr11:45153527..45160380-chr11:45165355..45169670,10	MCF-7	breast:
34	chr11:45153382..45155390-chr11:45160879..45163088,3	K562	blood:
35	chr11:45161924..45164749-chr11:45165739..45167752,2	MCF-7	breast:
36	chr11:45161325..45163624-chr11:45203172..45205696,2	K562	blood:
37	chr11:44971020..44974752-chr11:45167266..45169322,3	MCF-7	breast:
38	chr11:45179374..45181360-chr11:45184809..45187751,2	K562	blood:
39	chr11:45166402..45169959-chr11:45170699..45175813,6	MCF-7	breast:
40	chr11:45173226..45176543-chr11:45176880..45179156,4	K562	blood:
41	chr11:45153382..45155390-chr11:45160879..45163088,3	K562	blood:
42	chr11:45149822..45152040-chr11:45158984..45160669,2	MCF-7	breast:
43	chr11:45173610..45176134-chr11:45184836..45187202,2	K562	blood:
44	chr10:70747303..70749893-chr11:45167896..45169684,2	MCF-7	breast:
45	chr11:45167650..45170338-chr11:45189685..45192446,3	MCF-7	breast:
46	chr11:45176255..45180138-chr11:45180420..45184771,5	MCF-7	breast:
47	chr11:45168582..45169343-chr6:26157874..26158814,2	HCT-116	colon:
48	chr11:45173610..45176134-chr11:45184836..45187202,2	K562	blood:
49	chr11:45184562..45186695-chr11:45200479..45203077,3	MCF-7	breast:
50	chr11:45167891..45170733-chr11:45184381..45188024,4	K562	blood:

No data

Variant related genes	Relation type
PRDM11	TF binding region
PRDM11	CpG island
ENSG00000198954	chromatin interactions
ENSG00000121671	chromatin interactions
ENSG00000157570	chromatin interactions
ENSG00000158050	chromatin interactions
ENSG00000155542	chromatin interactions
ENSG00000175274	chromatin interactions
ENSG00000019485	chromatin interactions
ENSG00000203684	chromatin interactions
ENSG00000158373	chromatin interactions

Extended variants
information (count: 1413 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:1413 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs147059295	chr11:45154362-45154363	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs530540299	chr11:45154373-45154374	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs564598710	chr11:45154448-45154449	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs563727194	chr11:45154449-45154450	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs189529894	chr11:45154527-45154528	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs372781574	chr11:45154531-45154532	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs550122408	chr11:45154680-45154681	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs181834456	chr11:45154703-45154704	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs529570426	chr11:45154714-45154715	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs549308217	chr11:45154757-45154758	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs138436145	chr11:45154778-45154779	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs143915020	chr11:45154815-45154816	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs533571716	chr11:45154855-45154856	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs553438024	chr11:45154864-45154865	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs570471840	chr11:45154900-45154901	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs10769120	chr11:45154901-45154902	Inactive region	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs561129303	chr11:45154940-45154941	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs556090492	chr11:45154947-45154948	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs576244753	chr11:45154973-45154974	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs184552867	chr11:45154982-45154983	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs555742696	chr11:45155053-45155054	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs190084557	chr11:45155124-45155125	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs181701997	chr11:45155136-45155137	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs564535546	chr11:45155153-45155154	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs533286385	chr11:45155165-45155166	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs531064221	chr11:45155238-45155239	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs79307264	chr11:45155265-45155266	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs563722888	chr11:45155275-45155276	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs529538468	chr11:45155280-45155281	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs549244643	chr11:45155282-45155283	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs186759848	chr11:45155388-45155389	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs6485591	chr11:45155411-45155412	Bivalent Enhancer Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs371643588	chr11:45155415-45155416	Bivalent Enhancer Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs554692102	chr11:45155477-45155478	Bivalent Enhancer Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs570482936	chr11:45155485-45155486	Bivalent Enhancer Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs73464565	chr11:45155490-45155491	Bivalent Enhancer Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs191104127	chr11:45155511-45155512	Bivalent Enhancer Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs77046428	chr11:45155536-45155537	Bivalent Enhancer Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs147181961	chr11:45155555-45155556	Bivalent Enhancer Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs532356426	chr11:45155574-45155575	Bivalent Enhancer Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs180977254	chr11:45155580-45155581	Bivalent Enhancer Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs184934001	chr11:45155587-45155588	Bivalent Enhancer Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs116326901	chr11:45155588-45155589	Bivalent Enhancer Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs190966198	chr11:45155680-45155681	Bivalent Enhancer Flanking Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs60889303	chr11:45155739-45155740	Bivalent Enhancer Flanking Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs398055216	chr11:45155743-45155744	Bivalent Enhancer Flanking Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs569341641	chr11:45155768-45155769	Bivalent Enhancer Flanking Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs578001880	chr11:45155795-45155796	Bivalent Enhancer Flanking Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs543551434	chr11:45155823-45155824	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs148250666	chr11:45155833-45155834	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:60)

Disease	PMID	Source
Parathyroid adenoma	22454399	CNVD
Medulloblastoma	21979893	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
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Autism	22495311	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
Renal cell carcinoma	18194544	CNVD
Breast cancer	17603634	CNVD
Chordoma	18071362	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	21364760	CNVD
Potocki-Shaffer syndrome	19222835	CNVD
WAGR syndrome	19222835	CNVD
small cell lung cancer	20016488	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Myelofibrosis	22110671	CNVD
Melanoma	18172304	CNVD
Intracranial ependymoma	16609018	CNVD
Myxofibrosarcoma	16751306	CNVD
Potocki-Shaffer syndrome	22470819	CNVD
Neurodevelopmental disorder	22521361	CNVD
Breast cancer	16608533	CNVD
Hirschsprung''s Disease	21712996	CNVD
Follicular lymphoma	20505157	CNVD
Colorectal cancer	21128281	CNVD
Breast cancer	20409316	CNVD
Neurocytoma	17123091	CNVD
Central neurocytomas	17123091	CNVD
Multiple myeloma	16616336	CNVD
Cancer	17160897	CNVD
Mantle cell lymphoma	19029149	CNVD
Glioblastoma multiforme	21138945	CNVD
Prostate cancer	18632612	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:1212 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:45155000-45156000	Enhancers	Hela-S3	cervix
2	chr11:45155400-45155800	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin02	Skin
3	chr11:45155400-45155800	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin03	Skin
4	chr11:45155400-45155800	Enhancers	NHEK	skin
5	chr11:45155600-45155800	Flanking Active TSS	A549	lung
6	chr11:45161800-45162200	Enhancers	K562	blood
7	chr11:45162400-45163400	Enhancers	Primary hematopoietic stem cells short term culture	blood
8	chr11:45162800-45163600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
9	chr11:45162800-45163600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chr11:45163800-45164000	Bivalent Enhancer	Fetal Muscle Leg	muscle
11	chr11:45163800-45164400	Enhancers	Fetal Muscle Trunk	muscle
12	chr11:45163800-45164600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr11:45164000-45164200	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
14	chr11:45164000-45164200	Enhancers	Right Atrium	heart
15	chr11:45164000-45164200	Enhancers	Skeletal Muscle Female	skeletal muscle
16	chr11:45164000-45164600	Enhancers	NHEK	skin
17	chr11:45164000-45164800	Enhancers	Fetal Muscle Leg	muscle
18	chr11:45164200-45167000	Weak transcription	Right Atrium	heart
19	chr11:45164400-45167000	Weak transcription	Skeletal Muscle Female	skeletal muscle
20	chr11:45165600-45166000	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr11:45166200-45167000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr11:45166600-45166800	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
23	chr11:45166600-45166800	Enhancers	Brain Hippocampus Middle	brain
24	chr11:45166800-45167000	Bivalent/Poised TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr11:45166800-45167000	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
26	chr11:45166800-45167000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
27	chr11:45166800-45167000	Bivalent Enhancer	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr11:45166800-45167000	Enhancers	Breast Myoepithelial Primary Cells	Breast
29	chr11:45166800-45167000	Bivalent/Poised TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
30	chr11:45166800-45167000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
31	chr11:45166800-45167000	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
32	chr11:45166800-45167000	Active TSS	Brain Anterior Caudate	brain
33	chr11:45166800-45167000	Enhancers	Brain Inferior Temporal Lobe	brain
34	chr11:45166800-45167000	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
35	chr11:45166800-45167000	Bivalent Enhancer	Fetal Lung	lung
36	chr11:45166800-45167200	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
37	chr11:45166800-45167200	Flanking Bivalent TSS/Enh	H1 Cell Line	embryonic stem cell
38	chr11:45166800-45167200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
39	chr11:45166800-45167200	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
40	chr11:45166800-45167200	Bivalent Enhancer	Primary T cells from cord blood	blood
41	chr11:45166800-45167200	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr11:45166800-45167200	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
43	chr11:45166800-45167200	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
44	chr11:45166800-45167200	Bivalent Enhancer	Fetal Brain Female	brain
45	chr11:45166800-45167200	Enhancers	Fetal Intestine Small	intestine
46	chr11:45166800-45167200	Enhancers	Rectal Mucosa Donor 31	rectum
47	chr11:45166800-45167400	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
48	chr11:45166800-45167400	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
49	chr11:45166800-45167400	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
50	chr11:45166800-45167400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell

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