Variant report

Variant	nsv897897
Chromosome Location	chr11:71088949-71217571
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2545)
CpG islands
(count:5382)
Chromatin interactive
region (count:135)
LncRNA
region (count:13)
Mature miRNA
region (count: 2)
miRNA target
sites (count:0)

(count:2545 , 50 per page) page: 1 2 3 4 5 6 7 ... 51

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:71159395-71159730	HepG2	liver:	n/a	n/a
2	ARID3A	chr11:71160951-71161088	K562	blood:	n/a	n/a
3	ARID3A	chr11:71158261-71158580	HepG2	liver:	n/a	n/a
4	ARID3A	chr11:71161584-71161841	HepG2	liver:	n/a	n/a
5	ARID3A	chr11:71144739-71144757	HepG2	liver:	n/a	n/a
6	ARID3A	chr11:71159482-71159803	K562	blood:	n/a	n/a
7	ARID3A	chr11:71140352-71140466	HepG2	liver:	n/a	n/a
8	ARID3A	chr11:71131580-71131838	K562	blood:	n/a	n/a
9	ATF1	chr11:71113918-71114253	K562	blood:	n/a	n/a
10	ATF1	chr11:71159298-71159956	K562	blood:	n/a	n/a
11	ATF1	chr11:71160559-71161136	K562	blood:	n/a	n/a
12	ATF1	chr11:71121445-71121846	K562	blood:	n/a	n/a
13	ATF1	chr11:71103739-71103878	K562	blood:	n/a	n/a
14	ATF2	chr11:71159204-71159548	H1-hESC	embryonic stem cell:	n/a	n/a
15	ATF2	chr11:71159188-71159850	H1-hESC	embryonic stem cell:	n/a	n/a
16	ATF2	chr11:71159258-71159690	GM12878	blood:	n/a	n/a
17	ATF2	chr11:71159221-71159697	GM12878	blood:	n/a	n/a
18	ATF2	chr11:71200262-71200721	GM12878	blood:	n/a	n/a
19	ATF3	chr11:71095654-71095897	K562	blood:	n/a	n/a
20	ATF3	chr11:71159564-71159941	K562	blood:	n/a	chr11:71159709-71159729
21	BACH1	chr11:71215809-71215924	H1-hESC	embryonic stem cell:	n/a	n/a
22	BACH1	chr11:71163899-71163977	K562	blood:	n/a	n/a
23	BACH1	chr11:71098510-71099819	H1-hESC	embryonic stem cell:	n/a	n/a
24	BACH1	chr11:71158921-71159910	H1-hESC	embryonic stem cell:	n/a	n/a
25	BACH1	chr11:71098597-71099809	K562	blood:	n/a	n/a
26	BATF	chr11:71200324-71200707	GM12878	blood:	n/a	chr11:71200539-71200550
27	BCL11A	chr11:71129809-71130088	GM12878	blood:	n/a	n/a
28	BCL11A	chr11:71091457-71091688	GM12878	blood:	n/a	n/a
29	BCL3	chr11:71195121-71195384	GM12878	blood:	n/a	n/a
30	BCL3	chr11:71164062-71164876	A549	lung:	n/a	chr11:71164307-71164320 chr11:71164436-71164445 chr11:71164439-71164448
31	BCL3	chr11:71195483-71196158	GM12878	blood:	n/a	n/a
32	BCL3	chr11:71195577-71196144	GM12878	blood:	n/a	n/a
33	BCLAF1	chr11:71094502-71094906	GM12878	blood:	n/a	chr11:71094684-71094693
34	BCLAF1	chr11:71094470-71094945	GM12878	blood:	n/a	chr11:71094684-71094693
35	BHLHE40	chr11:71163260-71165062	GM12878	blood:	n/a	n/a
36	BHLHE40	chr11:71159967-71160275	HepG2	liver:	n/a	n/a
37	BHLHE40	chr11:71200401-71200653	GM12878	blood:	n/a	n/a
38	BHLHE40	chr11:71159278-71159865	GM12878	blood:	n/a	chr11:71159577-71159593
39	BHLHE40	chr11:71164289-71165095	K562	blood:	n/a	n/a
40	BHLHE40	chr11:71094591-71094797	GM12878	blood:	n/a	n/a
41	BHLHE40	chr11:71163833-71164054	K562	blood:	n/a	n/a
42	BHLHE40	chr11:71129894-71130027	GM12878	blood:	n/a	n/a
43	BHLHE40	chr11:71162977-71163210	K562	blood:	n/a	n/a
44	BHLHE40	chr11:71199259-71199455	K562	blood:	n/a	n/a
45	BHLHE40	chr11:71131531-71131751	K562	blood:	n/a	n/a
46	BHLHE40	chr11:71144741-71144795	K562	blood:	n/a	n/a
47	BHLHE40	chr11:71159271-71160321	K562	blood:	n/a	chr11:71159577-71159593
48	BHLHE40	chr11:71158933-71159040	K562	blood:	n/a	chr11:71159014-71159030
49	BRCA1	chr11:71159749-71159968	GM12878	blood:	n/a	n/a
50	BRCA1	chr11:71121368-71121550	Hela-S3	cervix:	n/a	n/a

(count:5382 , 50 per page) page: 1 2 3 4 5 6 7 ... 108

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:71164601-71164651	IMR90	lung:	fetal
2	chr11:71215361-71215411	HCT-116	colon:	n/a
3	chr11:71117753-71117803	T-47D	breast:	n/a
4	chr11:71150315-71150365	K562	blood:	n/a
5	chr11:71209518-71209568	T-47D	breast:	n/a
6	chr11:71164106-71164156	BE2_C	brain:	n/a
7	chr11:71163555-71163605	Hepatocyte	liver:	n/a
8	chr11:71185116-71185166	ovcar-3	ovarian:	n/a
9	chr11:71117679-71117729	SK-N-SH_RA	brain:	n/a
10	chr11:71146658-71146708	HEK293	kidney:	embryo
11	chr11:71175039-71175089	U87	brain:	n/a
12	chr11:71202329-71202379	SK-N-SH	brain:	n/a
13	chr11:71155081-71155131	PFSK-1	brain:	n/a
14	chr11:71164098-71164148	BJ	skin:	n/a
15	chr11:71164601-71164651	IMR90	lung:	fetal
16	chr11:71215361-71215411	HCT-116	colon:	n/a
17	chr11:71117753-71117803	T-47D	breast:	n/a
18	chr11:71150315-71150365	K562	blood:	n/a
19	chr11:71209518-71209568	T-47D	breast:	n/a
20	chr11:71164106-71164156	BE2_C	brain:	n/a
21	chr11:71163555-71163605	Hepatocyte	liver:	n/a
22	chr11:71185116-71185166	ovcar-3	ovarian:	n/a
23	chr11:71117679-71117729	SK-N-SH_RA	brain:	n/a
24	chr11:71146658-71146708	HEK293	kidney:	embryo
25	chr11:71175039-71175089	U87	brain:	n/a
26	chr11:71202329-71202379	SK-N-SH	brain:	n/a
27	chr11:71155081-71155131	PFSK-1	brain:	n/a
28	chr11:71164098-71164148	BJ	skin:	n/a
29	chr11:71201682-71201732	T-47D	breast:	n/a
30	chr11:71196591-71196641	HRPEpiC	eye:	n/a
31	chr11:71150200-71150250	GM12878	blood:	n/a
32	chr11:71196591-71196641	HCM	heart:	n/a
33	chr11:71174976-71175026	SK-N-MC	brain:	n/a
34	chr11:71210210-71210260	NB4	blood:	n/a
35	chr11:71164262-71164312	PANC-1	pancreas:	n/a
36	chr11:71212402-71212452	HEEpiC	esophagus:	n/a
37	chr11:71189490-71189540	HUVEC	blood vessel:	n/a
38	chr11:71155081-71155131	NB4	blood:	n/a
39	chr11:71164262-71164312	HAEpiC	amniotic membrane:	n/a
40	chr11:71189490-71189540	HCT-116	colon:	n/a
41	chr11:71150315-71150365	PrEC	prostate:	n/a
42	chr11:71164349-71164399	AG09309	skin:	n/a
43	chr11:71145665-71145715	Jurkat	blood:	n/a
44	chr11:71146456-71146506	T-47D	breast:	n/a
45	chr11:71209518-71209568	NT2-D1	testis:	n/a
46	chr11:71167505-71167555	CMK	blood:	n/a
47	chr11:71175039-71175089	HPAEpiC	pulmonary alveolar:	n/a
48	chr11:71187445-71187495	HEK293	kidney:	embryo
49	chr11:71202368-71202418	SK-N-SH	brain:	n/a
50	chr11:71202794-71202844	BE2_C	brain:	n/a

(count:135 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr11:70606031..70606654-chr11:71192416..71193099,3	MCF-7	breast:
2	chr11:71156994..71165841-chr11:71185066..71202614,31	MCF-7	breast:
3	chr11:71130483..71134539-chr11:71135016..71139274,7	MCF-7	breast:
4	chr11:71163622..71164449-chr15:73075829..73076683,2	NB4	blood:
5	chr11:71205951..71209347-chr11:71211780..71215363,4	MCF-7	breast:
6	chr11:71164184..71164815-chr17:58469519..58470423,2	MCF-7	breast:
7	chr11:71159580..71163175-chr11:71169801..71173356,4	MCF-7	breast:
8	chr11:71118859..71120385-chr11:71125434..71128124,2	MCF-7	breast:
9	chr11:71111891..71114927-chr11:71116804..71119287,3	K562	blood:
10	chr11:71083691..71084429-chr11:71131113..71131671,2	MCF-7	breast:
11	chr11:71192234..71193164-chr11:71211678..71212297,4	MCF-7	breast:
12	chr11:71212078..71213595-chr11:71215421..71217314,2	K562	blood:
13	chr11:71083987..71085496-chr11:71108216..71110305,2	MCF-7	breast:
14	chr11:71186512..71188685-chr11:71191239..71193061,2	K562	blood:
15	chr11:71166687..71169492-chr11:71189793..71191469,2	MCF-7	breast:
16	chr11:71137158..71140424-chr11:71155885..71157748,3	K562	blood:
17	chr11:71163908..71164465-chr11:71192678..71193270,2	MCF-7	breast:
18	chr11:71176264..71179140-chr11:71273245..71275842,2	MCF-7	breast:
19	chr11:71138911..71140880-chr11:71154532..71157322,2	K562	blood:
20	chr11:71137158..71140424-chr11:71155885..71157748,3	K562	blood:
21	chr11:71162324..71166430-chr11:71186520..71190924,4	K562	blood:
22	chr11:70805722..70807297-chr11:71158455..71160766,2	MCF-7	breast:
23	chr11:71122603..71125509-chr11:71135103..71137138,2	K562	blood:
24	chr11:71170457..71172341-chr11:71179212..71180985,2	K562	blood:
25	chr11:71177769..71179272-chr11:71180854..71183536,2	K562	blood:
26	chr11:71138540..71142714-chr11:71144455..71147360,4	K562	blood:
27	chr11:69329817..69330348-chr11:71192258..71193060,2	MCF-7	breast:
28	chr11:71144482..71146798-chr11:71158407..71160975,3	K562	blood:
29	chr11:71137647..71140040-chr11:71141812..71145984,4	K562	blood:
30	chr11:71209374..71211618-chr11:71213015..71214853,2	K562	blood:
31	chr11:71162324..71166430-chr11:71186520..71190924,4	K562	blood:
32	chr11:71169153..71171871-chr15:71407229..71409186,2	MCF-7	breast:
33	chr11:71209374..71211618-chr11:71213015..71214853,2	K562	blood:
34	chr11:71139168..71142453-chr11:71148977..71152491,3	K562	blood:
35	chr11:71192234..71193164-chr11:71211678..71212297,4	MCF-7	breast:
36	chr11:71171741..71174523-chr11:71191219..71193247,2	MCF-7	breast:
37	chr11:71157940..71161417-chr11:71161465..71165970,9	K562	blood:
38	chr11:70962836..70963538-chr11:71192225..71192780,2	MCF-7	breast:
39	chr11:71156994..71165841-chr11:71185066..71202614,31	MCF-7	breast:
40	chr11:70652696..70654215-chr11:71163128..71165343,2	MCF-7	breast:
41	chr11:7613542..7614042-chr11:71192235..71192736,2	MCF-7	breast:
42	chr11:70982645..70985292-chr11:71142311..71143975,2	MCF-7	breast:
43	chr11:71167353..71169049-chr11:71183186..71185493,2	K562	blood:
44	chr11:71138911..71140880-chr11:71154532..71157322,2	K562	blood:
45	chr11:71168777..71171362-chr11:71186051..71188733,3	MCF-7	breast:
46	chr11:71100930..71102789-chr11:71115222..71118166,2	MCF-7	breast:
47	chr11:71144398..71146962-chr11:71155881..71158329,2	K562	blood:
48	chr11:71091514..71093926-chr11:71098118..71101181,3	MCF-7	breast:
49	chr11:71122603..71125509-chr11:71135103..71137138,2	K562	blood:
50	chr11:71214959..71216939-chr11:71218643..71221307,2	K562	blood:

(count:13 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KRTAP5-7-1	chr11:71214591-71214787	NONHSAT022689
2	lnc-DHCR7-4	chr11:71217107-71217426	NONHSAT022691
3	lnc-NADSYN1-1	chr11:71162736-71164062	NONHSAT022678
4	lnc-DHCR7-3	chr11:71134380-71134469	NONHSAT022677
5	lnc-KRTAP5-7-1	chr11:71214910-71216920	NONHSAT022690
6	lnc-NADSYN1-1	chr11:71162736-71163182	XLOC_009199
7	lnc-NADSYN1-1	chr11:71162736-71163203	ENSG00000254682.1
8	lnc-NADSYN1-1	chr11:71159586-71159931	XLOC_009199
9	lnc-DHCR7-3	chr11:71125206-71125471	NONHSAT022677
10	lnc-NADSYN1-1	chr11:71159720-71159931	ENSG00000254682.1
11	lnc-DHCR7-3	chr11:71132847-71132950	NONHSAT022677
12	lnc-KRTAP5-7-1	chr11:71215112-71215524	NONHSAT022689
13	lnc-NADSYN1-1	chr11:71159587-71159931	NONHSAT022678

miRNA name	Chromosome Location	mirBase accession
hsa-miR-6754-3p	chr11:71184592-71184613	MIMAT0027409
hsa-miR-6754-5p	chr11:71184554-71184575	MIMAT0027408

No data

Variant related genes	Relation type
ENSG00000172900	TF binding region
ENSG00000254682	TF binding region
NADSYN1	TF binding region
ENSG00000254924	TF binding region
DHCR7	TF binding region
ENSG00000172900	CpG island
ENSG00000254682	CpG island
NADSYN1	CpG island
ENSG00000254924	CpG island
DHCR7	CpG island
ENSG00000249387	chromatin interactions
ENSG00000170832	chromatin interactions
ENSG00000172893	chromatin interactions
ENSG00000162105	chromatin interactions
ENSG00000172900	chromatin interactions
ENSG00000254924	chromatin interactions
ENSG00000105669	chromatin interactions
ENSG00000172890	chromatin interactions
ENSG00000196497	chromatin interactions
ENSG00000225362	chromatin interactions
ENSG00000204572	chromatin interactions
ENSG00000254682	chromatin interactions
ENSG00000141371	chromatin interactions
ENSG00000159322	chromatin interactions

Extended variants
information (count: 6195 )
Associated
traits (count: 105 )

Variant overlapped rSNPs/rCNVs (count:6195 , 50 per page) page: 1 2 3 4 5 6 7 ... 124

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs563852097	chr11:71088968-71088969	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs559415016	chr11:71088973-71088974	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs533239781	chr11:71089030-71089031	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs80013972	chr11:71089045-71089046	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs569860460	chr11:71089074-71089075	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs111740150	chr11:71089082-71089083	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs1660892	chr11:71089147-71089148	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs189727131	chr11:71089150-71089151	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs540229972	chr11:71089154-71089155	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs1620013	chr11:71089210-71089211	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
11	rs118060803	chr11:71089227-71089228	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs181275015	chr11:71089261-71089262	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs1790338	chr11:71089270-71089271	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs185797563	chr11:71089274-71089275	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs113154796	chr11:71089282-71089283	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs115541675	chr11:71089310-71089311	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs76592064	chr11:71089403-71089404	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs573378352	chr11:71089407-71089408	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs539731948	chr11:71089426-71089427	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs569113359	chr11:71089449-71089450	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs540704078	chr11:71089463-71089464	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs533185386	chr11:71089484-71089485	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs148176886	chr11:71089489-71089490	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs181863409	chr11:71089490-71089491	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs563481631	chr11:71089502-71089503	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs556528373	chr11:71089587-71089588	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs143080585	chr11:71089598-71089599	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs550321908	chr11:71089666-71089667	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs12292350	chr11:71089699-71089700	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs368106485	chr11:71089706-71089707	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs534337223	chr11:71089727-71089728	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs112786280	chr11:71089736-71089737	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs61385087	chr11:71089737-71089738	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs115615441	chr11:71089747-71089748	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs397786697	chr11:71089749-71089750	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs547517564	chr11:71089773-71089774	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs146114007	chr11:71089793-71089794	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs61885881	chr11:71089880-71089881	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs79955390	chr11:71089896-71089897	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs186068794	chr11:71089920-71089921	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs569932482	chr11:71089958-71089959	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs140132338	chr11:71090015-71090016	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs555524741	chr11:71090049-71090050	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs573441828	chr11:71090050-71090051	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs111737500	chr11:71090051-71090052	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs184741445	chr11:71090054-71090055	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs527635349	chr11:71090062-71090063	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs534712364	chr11:71090072-71090073	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs201779758	chr11:71090076-71090077	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs141998424	chr11:71090100-71090101	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:105)

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
Lung cancer	18438408	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
Chordoma	21602918	CNVD
Metanephric adenoma	20802469	CNVD
Melanoma	18172304	CNVD
Breast cancer	21806811	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
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Breast cancer	21364760	CNVD
lymphocytic leukemia	21291569	CNVD
Myelofibrosis	22110671	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Cancer	22183965	CNVD
Melanoma	22183965	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Breast cancer	16620391	CNVD
Multiple myeloma	17550852	CNVD
Breast cancer	21785460	CNVD
Neuroblastoma	18923191	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Multiple myeloma	16616336	CNVD
Urothelial cell carcinoma	18451213	CNVD
Leukoplakia	24403051	CNVD
Prostate cancer	17217626	CNVD
Cancer	22429812	CNVD
small cell lung cancer	20016488	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	19812545	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:3676 , 50 per page) page: 1 2 3 4 5 6 7 ... 74

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:71085600-71092000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
2	chr11:71088800-71091800	Weak transcription	GM12878-XiMat	blood
3	chr11:71090400-71096000	Enhancers	Primary B cells from peripheral blood	blood
4	chr11:71090800-71091200	Enhancers	H9 Cell Line	embryonic stem cell
5	chr11:71091200-71095800	Enhancers	Primary B cells from cord blood	blood
6	chr11:71091800-71093000	Enhancers	GM12878-XiMat	blood
7	chr11:71092000-71092200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
8	chr11:71092000-71092200	Enhancers	Spleen	Spleen
9	chr11:71092200-71093000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
10	chr11:71092200-71093000	Weak transcription	Spleen	Spleen
11	chr11:71093000-71093200	Flanking Active TSS	GM12878-XiMat	blood
12	chr11:71093000-71093400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr11:71093000-71093600	Enhancers	Spleen	Spleen
14	chr11:71093000-71093800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
15	chr11:71093200-71093400	Enhancers	GM12878-XiMat	blood
16	chr11:71093400-71093600	Flanking Active TSS	GM12878-XiMat	blood
17	chr11:71093600-71094200	Enhancers	GM12878-XiMat	blood
18	chr11:71094200-71094800	Flanking Active TSS	GM12878-XiMat	blood
19	chr11:71094800-71095600	Enhancers	GM12878-XiMat	blood
20	chr11:71095600-71097800	Enhancers	Brain Cingulate Gyrus	brain
21	chr11:71095600-71098000	Enhancers	Brain Inferior Temporal Lobe	brain
22	chr11:71095800-71096200	Weak transcription	Primary B cells from cord blood	blood
23	chr11:71095800-71097000	Enhancers	Brain Hippocampus Middle	brain
24	chr11:71095800-71097800	Enhancers	Brain Angular Gyrus	brain
25	chr11:71095800-71098000	Enhancers	Brain Substantia Nigra	brain
26	chr11:71096000-71096400	Weak transcription	Primary B cells from peripheral blood	blood
27	chr11:71096200-71098400	Enhancers	Primary B cells from cord blood	blood
28	chr11:71096400-71099000	Enhancers	Primary B cells from peripheral blood	blood
29	chr11:71096600-71097000	Enhancers	Brain Anterior Caudate	brain
30	chr11:71097000-71097400	Weak transcription	Brain Hippocampus Middle	brain
31	chr11:71097400-71097800	Enhancers	Brain Hippocampus Middle	brain
32	chr11:71100000-71100200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
33	chr11:71100000-71101000	Enhancers	Breast Myoepithelial Primary Cells	Breast
34	chr11:71100200-71100400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
35	chr11:71100200-71101400	Bivalent Enhancer	Fetal Muscle Trunk	muscle
36	chr11:71100400-71100600	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin02	Skin
37	chr11:71100400-71100800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
38	chr11:71100400-71100800	Enhancers	Esophagus	oesophagus
39	chr11:71100400-71100800	Bivalent Enhancer	NHEK	skin
40	chr11:71100400-71102400	Enhancers	Fetal Muscle Leg	muscle
41	chr11:71100600-71100800	Bivalent Enhancer	Fetal Stomach	stomach
42	chr11:71100600-71101000	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin03	Skin
43	chr11:71101000-71101400	Enhancers	Esophagus	oesophagus
44	chr11:71101400-71102000	Enhancers	Primary B cells from peripheral blood	blood
45	chr11:71101600-71101800	Bivalent Enhancer	Primary B cells from cord blood	blood
46	chr11:71102400-71102600	Bivalent Enhancer	Placenta	Placenta
47	chr11:71102400-71102800	Enhancers	Pancreas	Pancrea
48	chr11:71102400-71102800	Enhancers	Small Intestine	intestine
49	chr11:71102400-71103000	Enhancers	HSMM	muscle
50	chr11:71102400-71103000	Enhancers	HSMMtube	muscle

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