Variant report

Variant	nsv897927
Chromosome Location	chr11:75866999-75908083
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:317)
CpG islands
(count:1037)
Chromatin interactive
region (count:51)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:317 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr11:75877442-75877843	GM12878	blood:	n/a	n/a
2	ATF2	chr11:75877385-75877776	GM12878	blood:	n/a	n/a
3	BATF	chr11:75880507-75880811	GM12878	blood:	n/a	n/a
4	BATF	chr11:75877503-75877745	GM12878	blood:	n/a	n/a
5	BATF	chr11:75880537-75880793	GM12878	blood:	n/a	n/a
6	BATF	chr11:75877452-75877791	GM12878	blood:	n/a	n/a
7	BCL11A	chr11:75880481-75880847	GM12878	blood:	n/a	chr11:75880797-75880806
8	BCL11A	chr11:75877450-75877789	GM12878	blood:	n/a	chr11:75877743-75877752
9	BCL11A	chr11:75877511-75877755	GM12878	blood:	n/a	chr11:75877743-75877752
10	BHLHE40	chr11:75868229-75868428	K562	blood:	n/a	n/a
11	BHLHE40	chr11:75874450-75874566	GM12878	blood:	n/a	chr11:75874506-75874515 chr11:75874499-75874520 chr11:75874505-75874514 chr11:75874505-75874514 chr11:75874504-75874513
12	BHLHE40	chr11:75874343-75874668	HepG2	liver:	n/a	chr11:75874506-75874515 chr11:75874499-75874520 chr11:75874505-75874514 chr11:75874505-75874514 chr11:75874504-75874513
13	BHLHE40	chr11:75877454-75877762	GM12878	blood:	n/a	n/a
14	BHLHE40	chr11:75880588-75880997	GM12878	blood:	n/a	n/a
15	BHLHE40	chr11:75874344-75874627	K562	blood:	n/a	chr11:75874506-75874515 chr11:75874499-75874520 chr11:75874505-75874514 chr11:75874505-75874514 chr11:75874504-75874513
16	BHLHE40	chr11:75895960-75896047	K562	blood:	n/a	n/a
17	BHLHE40	chr11:75879567-75879848	K562	blood:	n/a	n/a
18	CBX3	chr11:75873978-75874336	K562	blood:	n/a	n/a
19	CCNT2	chr11:75872492-75872651	K562	blood:	n/a	n/a
20	CCNT2	chr11:75895841-75896045	K562	blood:	n/a	n/a
21	CEBPB	chr11:75895861-75896066	K562	blood:	n/a	n/a
22	CEBPB	chr11:75901486-75901900	IMR90	lung:	n/a	n/a
23	CEBPD	chr11:75895671-75896175	K562	blood:	n/a	n/a
24	CHD2	chr11:75877442-75877713	GM12878	blood:	n/a	n/a
25	CHD2	chr11:75880552-75880866	GM12878	blood:	n/a	n/a
26	CTCF	chr11:75905984-75906019	GM12891	blood:	n/a	chr11:75905992-75906010 chr11:75905995-75906004 chr11:75905994-75906015
27	CTCF	chr11:75886940-75887090	HepG2	liver:	n/a	chr11:75886958-75886971
28	CTCF	chr11:75893277-75893382	H1-hESC	embryonic stem cell:	n/a	n/a
29	CTCF	chr11:75900080-75900230	WERI-Rb-1	eye:	n/a	n/a
30	CTCF	chr11:75866920-75867070	HCPEpiC	choroid plexus:	n/a	n/a
31	CTCF	chr11:75905924-75906068	H1-hESC	embryonic stem cell:	n/a	chr11:75905992-75906010 chr11:75905995-75906004 chr11:75905994-75906015
32	CTCF	chr11:75905880-75906030	BJ	skin:	n/a	chr11:75905992-75906010 chr11:75905995-75906004 chr11:75905994-75906015
33	CTCF	chr11:75905960-75905978	MCF-7	breast:	n/a	n/a
34	CTCF	chr11:75867680-75867830	NHDF-neo	bronchial:	n/a	n/a
35	CTCF	chr11:75875782-75875840	Spleen_OC	spleen:	n/a	n/a
36	CTCF	chr11:75893388-75893447	K562	blood:	n/a	n/a
37	CTCF	chr11:75867700-75867850	BE2_C	brain:	n/a	n/a
38	CTCF	chr11:75893351-75893483	Hela-S3	cervix:	n/a	n/a
39	CTCF	chr11:75868040-75868190	SK-N-SH_RA	brain:	n/a	n/a
40	CTCF	chr11:75892540-75892690	Caco-2	colon:	n/a	chr11:75892629-75892637
41	CTCF	chr11:75897240-75897390	AG09319	gingival:	n/a	n/a
42	CTCF	chr11:75900080-75900230	HUVEC	blood vessel:	n/a	n/a
43	CTCF	chr11:75905988-75905993	MCF-7	breast:	n/a	n/a
44	CTCF	chr11:75866860-75867010	BE2_C	brain:	n/a	n/a
45	CTCF	chr11:75892487-75892684	H1-hESC	embryonic stem cell:	n/a	chr11:75892629-75892637
46	CTCF	chr11:75886860-75887010	AG04449	skin:	n/a	chr11:75886958-75886971
47	CTCF	chr11:75897220-75897370	BE2_C	brain:	n/a	n/a
48	CTCF	chr11:75873900-75874050	WERI-Rb-1	eye:	n/a	n/a
49	CTCF	chr11:75867860-75868010	BE2_C	brain:	n/a	n/a
50	CTCF	chr11:75893220-75893370	Caco-2	colon:	n/a	n/a

(count:1037 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:75898203-75898253	HNPCEpiC	eye:	n/a
2	chr11:75878127-75878177	HRCEpiC	kidney:	n/a
3	chr11:75905850-75905900	HNPCEpiC	eye:	n/a
4	chr11:75897427-75897477	SK-N-SH	brain:	n/a
5	chr11:75898203-75898253	CMK	blood:	n/a
6	chr11:75898203-75898253	HL-60	blood:	n/a
7	chr11:75898132-75898182	Jurkat	blood:	n/a
8	chr11:75907205-75907255	HCPEpiC	choroid plexus:	n/a
9	chr11:75873027-75873077	ProgFib	skin:	n/a
10	chr11:75898132-75898182	A549	lung:	n/a
11	chr11:75897427-75897477	Jurkat	blood:	n/a
12	chr11:75878127-75878177	LNCaP	prostate:	n/a
13	chr11:75897427-75897477	HMEC	breast:	n/a
14	chr11:75907205-75907255	NHBE	bronchial:	n/a
15	chr11:75876135-75876185	HCF	heart:	n/a
16	chr11:75898203-75898253	K562	blood:	n/a
17	chr11:75879348-75879398	CMK	blood:	n/a
18	chr11:75898132-75898182	NB4	blood:	n/a
19	chr11:75905917-75905967	HRE	kidney:	n/a
20	chr11:75902270-75902320	BE2_C	brain:	n/a
21	chr11:75873027-75873077	HCF	heart:	n/a
22	chr11:75896332-75896382	HUVEC	blood vessel:	n/a
23	chr11:75898132-75898182	HRPEpiC	eye:	n/a
24	chr11:75898195-75898245	RPTEC	kidney:	n/a
25	chr11:75898132-75898182	BE2_C	brain:	n/a
26	chr11:75905917-75905967	GM12891	blood:	n/a
27	chr11:75902270-75902320	HUVEC	blood vessel:	n/a
28	chr11:75905917-75905967	Jurkat	blood:	n/a
29	chr11:75898132-75898182	NHDF-neo	bronchial:	n/a
30	chr11:75896332-75896382	AG04450	lung:	fetal
31	chr11:75905917-75905967	PrEC	prostate:	n/a
32	chr11:75875926-75875976	AG09309	skin:	n/a
33	chr11:75898132-75898182	SK-N-SH	brain:	n/a
34	chr11:75907205-75907255	SK-N-MC	brain:	n/a
35	chr11:75875926-75875976	SK-N-SH	brain:	n/a
36	chr11:75897427-75897477	PANC-1	pancreas:	n/a
37	chr11:75902270-75902320	BJ	skin:	n/a
38	chr11:75879348-75879398	HRPEpiC	eye:	n/a
39	chr11:75898132-75898182	HCT-116	colon:	n/a
40	chr11:75905718-75905768	ovcar-3	ovarian:	n/a
41	chr11:75898195-75898245	HepG2	liver:	n/a
42	chr11:75905718-75905768	NHDF-neo	bronchial:	n/a
43	chr11:75875926-75875976	NH-A	brain:	n/a
44	chr11:75875926-75875976	AG04449	skin:	fetal
45	chr11:75876135-75876185	HRCEpiC	kidney:	n/a
46	chr11:75879348-75879398	MCF-7	breast:	n/a
47	chr11:75898203-75898253	GM12878	blood:	n/a
48	chr11:75904184-75904234	Hepatocyte	liver:	n/a
49	chr11:75878127-75878177	HUVEC	blood vessel:	n/a
50	chr11:75876135-75876185	ECC-1	luminal epithelium:	n/a

(count:51 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr11:75879470..75881382-chr11:75903439..75906024,2	MCF-7	breast:
2	chr11:75864528..75867031-chr11:75871798..75873454,2	K562	blood:
3	chr11:75898285..75900069-chr11:75902238..75904019,2	K562	blood:
4	chr11:75904809..75906919-chr11:75917526..75920230,2	K562	blood:
5	chr11:75907802..75910235-chr11:75912499..75914692,2	K562	blood:
6	chr11:75872410..75875308-chr11:75879381..75883436,3	K562	blood:
7	chr11:75902153..75903768-chr11:75945033..75947723,2	K562	blood:
8	chr11:75878808..75880535-chr11:75885544..75887523,2	K562	blood:
9	chr11:75886513..75888497-chr11:75907057..75909283,2	MCF-7	breast:
10	chr11:75864528..75867031-chr11:75871798..75873454,2	K562	blood:
11	chr11:75888382..75891358-chr11:75893738..75896231,2	MCF-7	breast:
12	chr11:75886513..75888497-chr11:75907057..75909283,2	MCF-7	breast:
13	chr11:75901884..75904848-chr11:76015737..76018383,2	MCF-7	breast:
14	chr11:75891012..75893171-chr11:75895940..75897806,2	K562	blood:
15	chr11:75892849..75895480-chr11:75897932..75899434,2	K562	blood:
16	chr11:75881616..75884148-chr11:75897760..75900480,2	MCF-7	breast:
17	chr11:75895025..75897686-chr11:75910991..75913944,2	K562	blood:
18	chr11:75892849..75895480-chr11:75897932..75899434,2	K562	blood:
19	chr11:75887769..75890550-chr11:75903812..75906303,2	K562	blood:
20	chr11:75865596..75868388-chr11:75876534..75879243,2	K562	blood:
21	chr11:75871119..75872885-chr11:75874380..75876840,2	MCF-7	breast:
22	chr11:75877596..75879712-chr11:75888366..75889930,2	K562	blood:
23	chr11:75896186..75898075-chr11:75909574..75912491,2	K562	blood:
24	chr11:75886596..75888940-chr11:75889618..75892110,2	MCF-7	breast:
25	chr11:75892849..75895759-chr11:75897789..75899434,2	K562	blood:
26	chr11:75871119..75872885-chr11:75874380..75876840,2	MCF-7	breast:
27	chr11:75878808..75880535-chr11:75885544..75887523,2	K562	blood:
28	chr11:75867883..75870652-chr11:75871506..75874252,2	MCF-7	breast:
29	chr11:75892849..75895759-chr11:75897789..75899434,2	K562	blood:
30	chr11:75895372..75898295-chr11:75906346..75908229,2	K562	blood:
31	chr11:75864698..75867155-chr11:75871013..75872936,2	MCF-7	breast:
32	chr11:75867883..75870652-chr11:75871506..75874252,2	MCF-7	breast:
33	chr11:75874099..75876373-chr11:75881253..75883763,2	MCF-7	breast:
34	chr11:75886596..75888940-chr11:75889618..75892110,2	MCF-7	breast:
35	chr11:75888382..75891358-chr11:75893738..75896231,2	MCF-7	breast:
36	chr11:75874099..75876373-chr11:75881253..75883763,2	MCF-7	breast:
37	chr11:75881616..75884148-chr11:75897760..75900480,2	MCF-7	breast:
38	chr11:75864698..75867155-chr11:75871013..75872936,2	MCF-7	breast:
39	chr11:75898285..75900069-chr11:75902238..75904019,2	K562	blood:
40	chr11:75901629..75903680-chr11:75921082..75923446,2	K562	blood:
41	chr11:75895372..75898295-chr11:75906346..75908229,2	K562	blood:
42	chr11:75872410..75875308-chr11:75879381..75883436,3	K562	blood:
43	chr11:75887769..75890550-chr11:75903812..75906303,2	K562	blood:
44	chr11:75891012..75893171-chr11:75895940..75897806,2	K562	blood:
45	chr11:75865596..75868388-chr11:75876534..75879243,2	K562	blood:
46	chr11:75858885..75860766-chr11:75865503..75867457,2	K562	blood:
47	chr11:75879470..75881382-chr11:75903439..75906024,2	MCF-7	breast:
48	chr11:75679088..75681419-chr11:75870768..75873220,2	K562	blood:
49	chr11:75877596..75879712-chr11:75888366..75889930,2	K562	blood:
50	chr11:75526830..75528448-chr11:75885826..75888721,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-UVRAG-2	chr11:75905685-75906115	ENSG00000254933.1
2	lnc-UVRAG-2	chr11:75901769-75901950	ENSG00000254933.1

No data

Variant related genes	Relation type
ENSG00000254933	TF binding region
ENSG00000254933	CpG island
ENSG00000085741	chromatin interactions

Extended variants
information (count: 1888 )
Associated
traits (count: 99 )

Variant overlapped rSNPs/rCNVs (count:1888 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7106626	chr11:75866999-75867000	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs371895945	chr11:75867069-75867070	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
3	rs539521103	chr11:75867086-75867087	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
4	rs142770883	chr11:75867087-75867088	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
5	rs200172618	chr11:75867152-75867153	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
6	rs371916999	chr11:75867189-75867190	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
7	rs112992387	chr11:75867193-75867194	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
8	rs34240196	chr11:75867248-75867249	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs560000272	chr11:75867252-75867253	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs556780626	chr11:75867337-75867338	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs532313997	chr11:75867369-75867370	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs11236628	chr11:75867377-75867378	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs568667242	chr11:75867479-75867480	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs144713772	chr11:75867482-75867483	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs548231065	chr11:75867513-75867514	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs11236629	chr11:75867521-75867522	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs111693163	chr11:75867526-75867527	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs533758347	chr11:75867561-75867562	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs141706683	chr11:75867603-75867604	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs371201235	chr11:75867669-75867670	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs577601279	chr11:75867785-75867786	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs540182462	chr11:75867830-75867831	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
23	rs556898177	chr11:75867905-75867906	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
24	rs576540156	chr11:75867917-75867918	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
25	rs10899161	chr11:75867945-75867946	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs78224751	chr11:75867974-75867975	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
27	rs180916018	chr11:75868074-75868075	Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs10899162	chr11:75868099-75868100	Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs12294072	chr11:75868121-75868122	Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs533161354	chr11:75868218-75868219	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
31	rs11236630	chr11:75868241-75868242	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs150039112	chr11:75868259-75868260	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
33	rs11236631	chr11:75868266-75868267	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs10899163	chr11:75868279-75868280	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs545068727	chr11:75868288-75868289	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
36	rs145391193	chr11:75868311-75868312	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
37	rs144373745	chr11:75868339-75868340	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
38	rs149212374	chr11:75868423-75868424	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
39	rs560906644	chr11:75868424-75868425	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
40	rs553035139	chr11:75868473-75868474	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
41	rs539449403	chr11:75868479-75868480	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
42	rs556861301	chr11:75868487-75868488	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
43	rs186184464	chr11:75868491-75868492	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
44	rs112170149	chr11:75868504-75868505	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
45	rs140259430	chr11:75868529-75868530	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
46	rs374492410	chr11:75868532-75868533	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
47	rs541081585	chr11:75868543-75868544	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
48	rs572307730	chr11:75868606-75868607	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
49	rs147230800	chr11:75868635-75868636	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
50	rs564252327	chr11:75868637-75868638	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:99)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Wilms tumour	21544195	CNVD
Autism	22495311	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Glioblastoma multiforme	21138945	CNVD
Acute myeloid leukemia	20729466	CNVD
Acute lymphoblastic leukemia	20067559	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
Prostate cancer	18632612	CNVD
Smith-Lemli-Opitz syndrome	21572526	CNVD
Glioblastoma multiforme	21080181	CNVD
Multiple myeloma	16461302	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Melanoma	18172304	CNVD
Breast cancer	22002566	CNVD
Ductal carcinoma	18381933	CNVD
Retinoblastoma	22278416	CNVD
Breast cancer	20953835	CNVD
oto-dental syndrome	17656375	CNVD
Asthma	21956041	CNVD
Breast cancer	17603634	CNVD
Ovarian neoplasms	16753589	CNVD
Non-small cell lung cancer	20864512	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cervical cancer	21062161	CNVD
Breast cancer	21509527	CNVD
Breast cancer	17001317	CNVD
Oral squamous cell carcinoma	16619035	CNVD
Intracranial aneurysm	16715129	CNVD
Colorectal cancer	16272173	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Colorectal cancer	16882699	CNVD
Berardinelli-seip congenital generalized lipodystrophy	17668395	CNVD
Spinal muscular atrophy	17668395	CNVD
Neonatal seizures	17668395	CNVD
Neonatal seizures	17668391	CNVD
Neuroticism	17667963	CNVD
Cancer	17916600	CNVD
Squamous cell cancer	19047905	CNVD
Multiple endocrine neoplasia type 1	19566914	CNVD
XY sex reversal	17503084	CNVD
Berardinelli-seip congenital generalized lipodystrophy	17668391	CNVD
Maculopathy	17646752	CNVD
Breast cancer	17899364	CNVD
Breast cancer	17157792	CNVD
Esophageal squamous carcinoma	18350619	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
lymphocytic leukemia	21291569	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Cancer	22183965	CNVD
Melanoma	22183965	CNVD
Breast cancer	16620391	CNVD
Multiple myeloma	17550852	CNVD
Neuroblastoma	18923191	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Multiple myeloma	16616336	CNVD
Myelofibrosis	22110671	CNVD
Prostate cancer	17217626	CNVD
Cancer	22429812	CNVD
small cell lung cancer	20016488	CNVD
Acute myeloid leukemia	21251322	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21482786	CNVD
Ovarian cancer	20844748	CNVD
Breast cancer	16608533	CNVD
Usher syndrome	18421352	CNVD
Breast cancer	21858162	CNVD
Ovarian cancer	21240255	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:541 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:75833400-75872800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
2	chr11:75862800-75869200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr11:75864000-75868000	Weak transcription	Fetal Heart	heart
4	chr11:75864400-75868000	Weak transcription	Skeletal Muscle Female	skeletal muscle
5	chr11:75864400-75871800	Weak transcription	Right Atrium	heart
6	chr11:75864600-75872600	Weak transcription	Fetal Intestine Large	intestine
7	chr11:75864800-75868000	Weak transcription	Fetal Thymus	thymus
8	chr11:75865000-75868000	Enhancers	HepG2	liver
9	chr11:75865000-75868200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr11:75865000-75868800	Weak transcription	Skeletal Muscle Male	skeletal muscle
11	chr11:75865000-75869000	Weak transcription	Pancreas	Pancrea
12	chr11:75865000-75869600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr11:75865000-75876000	Weak transcription	Spleen	Spleen
14	chr11:75865200-75868000	Weak transcription	Placenta Amnion	Placenta Amnion
15	chr11:75865800-75870400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
16	chr11:75866400-75867200	Enhancers	Fetal Lung	lung
17	chr11:75866400-75867200	Bivalent Enhancer	Fetal Muscle Trunk	muscle
18	chr11:75866400-75867400	Enhancers	Adipose Nuclei	Adipose
19	chr11:75866600-75867200	Bivalent Enhancer	Fetal Muscle Leg	muscle
20	chr11:75866600-75867200	Enhancers	Placenta	Placenta
21	chr11:75866600-75868000	Enhancers	Fetal Stomach	stomach
22	chr11:75867200-75868200	Weak transcription	Fetal Lung	lung
23	chr11:75867200-75868200	Enhancers	Fetal Muscle Leg	muscle
24	chr11:75867400-75869000	Weak transcription	Adipose Nuclei	Adipose
25	chr11:75867800-75875200	Bivalent Enhancer	Fetal Muscle Trunk	muscle
26	chr11:75868000-75868200	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin02	Skin
27	chr11:75868000-75868200	Enhancers	Fetal Thymus	thymus
28	chr11:75868000-75868200	Enhancers	Skeletal Muscle Female	skeletal muscle
29	chr11:75868000-75868200	Flanking Active TSS	HepG2	liver
30	chr11:75868000-75868400	Enhancers	Placenta Amnion	Placenta Amnion
31	chr11:75868000-75868800	Enhancers	Fetal Heart	heart
32	chr11:75868000-75869200	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
33	chr11:75868000-75869800	Bivalent Enhancer	Fetal Stomach	stomach
34	chr11:75868200-75868400	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
35	chr11:75868200-75868400	Enhancers	HepG2	liver
36	chr11:75868200-75868600	Weak transcription	Skeletal Muscle Female	skeletal muscle
37	chr11:75868200-75869600	Enhancers	Fetal Lung	lung
38	chr11:75868200-75870400	Bivalent Enhancer	Fetal Muscle Leg	muscle
39	chr11:75868400-75869200	Bivalent Enhancer	HepG2	liver
40	chr11:75868600-75869200	Enhancers	Skeletal Muscle Female	skeletal muscle
41	chr11:75868800-75869200	Weak transcription	Fetal Heart	heart
42	chr11:75868800-75869200	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
43	chr11:75869000-75869200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
44	chr11:75869000-75869200	Enhancers	Pancreas	Pancrea
45	chr11:75869000-75869400	Enhancers	Adipose Nuclei	Adipose
46	chr11:75869200-75869400	Enhancers	Fetal Heart	heart
47	chr11:75869200-75869400	Enhancers	Skeletal Muscle Male	skeletal muscle
48	chr11:75869200-75869600	Weak transcription	Pancreas	Pancrea
49	chr11:75869200-75871600	Weak transcription	Skeletal Muscle Female	skeletal muscle
50	chr11:75869200-75874400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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