Variant report

Variant	nsv524611
Chromosome Location	chr11:17300844-17316029
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:71)
CpG islands
(count:61)
Chromatin interactive
region (count:15)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:71 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr11:17315495-17315916	GM12878	blood:	n/a	n/a
2	ATF2	chr11:17315464-17316124	GM12878	blood:	n/a	n/a
3	BATF	chr11:17315531-17315975	GM12878	blood:	n/a	n/a
4	BATF	chr11:17315562-17315887	GM12878	blood:	n/a	n/a
5	BCL11A	chr11:17315561-17315939	GM12878	blood:	n/a	n/a
6	BHLHE40	chr11:17307409-17307597	K562	blood:	n/a	n/a
7	CEBPB	chr11:17302077-17302365	IMR90	lung:	n/a	chr11:17302231-17302242
8	CEBPB	chr11:17302037-17302399	K562	blood:	n/a	chr11:17302231-17302242
9	CEBPB	chr11:17313606-17313609	HepG2	liver:	n/a	n/a
10	CEBPB	chr11:17304269-17304472	HepG2	liver:	n/a	chr11:17304409-17304420
11	CEBPB	chr11:17302029-17302414	Hela-S3	cervix:	n/a	chr11:17302231-17302242
12	CEBPB	chr11:17302088-17302280	A549	lung:	n/a	chr11:17302231-17302242
13	CEBPB	chr11:17302045-17302413	K562	blood:	n/a	chr11:17302231-17302242
14	CEBPB	chr11:17302044-17302398	HepG2	liver:	n/a	chr11:17302231-17302242
15	CEBPB	chr11:17304373-17304520	A549	lung:	n/a	chr11:17304409-17304420
16	EP300	chr11:17301968-17302394	K562	blood:	n/a	n/a
17	EP300	chr11:17302085-17302394	Hela-S3	cervix:	n/a	n/a
18	EP300	chr11:17315650-17315813	GM12878	blood:	n/a	n/a
19	FOS	chr11:17310857-17311012	MCF10A-Er-Src	breast:	n/a	n/a
20	FOXA1	chr11:17313297-17313537	T-47D	breast:	n/a	n/a
21	GABPA	chr11:17307316-17307821	HL-60	blood:	n/a	chr11:17307467-17307476
22	GATA3	chr11:17313239-17313524	T-47D	breast:	n/a	n/a
23	IKZF1	chr11:17314920-17315074	GM12878	blood:	n/a	n/a
24	IRF1	chr11:17314886-17315171	K562	blood:	n/a	chr11:17314918-17314927
25	IRF1	chr11:17300826-17301004	K562	blood:	n/a	n/a
26	IRF4	chr11:17315511-17315906	GM12878	blood:	n/a	n/a
27	JUND	chr11:17302063-17302358	K562	blood:	n/a	n/a
28	KAP1	chr11:17302057-17302260	HEK293	kidney:	n/a	n/a
29	MAFF	chr11:17314944-17315210	HepG2	liver:	n/a	chr11:17315065-17315083
30	MAFF	chr11:17313377-17313589	HepG2	liver:	n/a	chr11:17313478-17313496 chr11:17313477-17313491
31	MAFF	chr11:17314886-17315270	K562	blood:	n/a	chr11:17315065-17315083
32	MAFK	chr11:17313353-17313568	HepG2	liver:	n/a	chr11:17313482-17313496 chr11:17313474-17313494 chr11:17313477-17313491 chr11:17313476-17313492 chr11:17313479-17313495 chr11:17313484-17313495
33	MAFK	chr11:17314892-17315251	IMR90	lung:	n/a	chr11:17315066-17315081
34	MAFK	chr11:17314891-17315259	K562	blood:	n/a	chr11:17315066-17315081
35	MAFK	chr11:17313309-17313548	IMR90	lung:	n/a	chr11:17313482-17313496 chr11:17313474-17313494 chr11:17313477-17313491 chr11:17313476-17313492 chr11:17313479-17313495 chr11:17313484-17313495
36	MAFK	chr11:17314887-17315242	HepG2	liver:	n/a	chr11:17315066-17315081
37	MAFK	chr11:17314912-17315232	HepG2	liver:	n/a	chr11:17315066-17315081
38	MAFK	chr11:17314942-17315184	Hela-S3	cervix:	n/a	chr11:17315066-17315081
39	MAX	chr11:17314792-17315127	NB4	blood:	n/a	chr11:17314942-17314952
40	MEF2A	chr11:17315460-17315988	GM12878	blood:	n/a	n/a
41	MEF2A	chr11:17315459-17316051	GM12878	blood:	n/a	n/a
42	MYC	chr11:17314899-17315088	NB4	blood:	n/a	chr11:17314942-17314952
43	MYC	chr11:17302014-17302345	K562	blood:	n/a	chr11:17302234-17302243
44	NFIC	chr11:17315303-17316043	GM12878	blood:	n/a	n/a
45	NFIC	chr11:17315495-17316024	GM12878	blood:	n/a	n/a
46	POLR2A	chr11:17313496-17313819	MCF10A-Er-Src	breast:	n/a	n/a
47	POLR2A	chr11:17307260-17307835	HL-60	blood:	n/a	n/a
48	POLR2A	chr11:17303660-17303875	ProgFib	skin:	n/a	n/a
49	POLR2A	chr11:17307662-17307703	MCF-7	breast:	n/a	n/a
50	POLR2A	chr11:17307234-17307886	HL-60	blood:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:17300909-17300959	HEK293	kidney:	embryo
2	chr11:17300909-17300959	SK-N-SH	brain:	n/a
3	chr11:17300909-17300959	LNCaP	prostate:	n/a
4	chr11:17300909-17300959	NHBE	bronchial:	n/a
5	chr11:17300909-17300959	AG04449	skin:	fetal
6	chr11:17300909-17300959	NH-A	brain:	n/a
7	chr11:17300909-17300959	K562	blood:	n/a
8	chr11:17300909-17300959	SAEC	small airway:	n/a
9	chr11:17300909-17300959	HRCEpiC	kidney:	n/a
10	chr11:17300909-17300959	NT2-D1	testis:	n/a
11	chr11:17300909-17300959	SK-N-MC	brain:	n/a
12	chr11:17300909-17300959	HCPEpiC	choroid plexus:	n/a
13	chr11:17300909-17300959	PFSK-1	brain:	n/a
14	chr11:17300909-17300959	GM12891	blood:	n/a
15	chr11:17300909-17300959	HRPEpiC	eye:	n/a
16	chr11:17300909-17300959	Jurkat	blood:	n/a
17	chr11:17300909-17300959	Hela-S3	cervix:	n/a
18	chr11:17300909-17300959	HIPEpiC	eye:	n/a
19	chr11:17300909-17300959	HPAEpiC	pulmonary alveolar:	n/a
20	chr11:17300909-17300959	GM06990	blood:	n/a
21	chr11:17300909-17300959	PrEC	prostate:	n/a
22	chr11:17300909-17300959	HAEpiC	amniotic membrane:	n/a
23	chr11:17300909-17300959	GM12878	blood:	n/a
24	chr11:17300909-17300959	SKMC	muscle:	n/a
25	chr11:17300909-17300959	AG04450	lung:	fetal
26	chr11:17300909-17300959	H1-hESC	embryonic stem cell:	embryo
27	chr11:17300909-17300959	HL-60	blood:	n/a
28	chr11:17300909-17300959	CMK	blood:	n/a
29	chr11:17300909-17300959	NHDF-neo	bronchial:	n/a
30	chr11:17300909-17300959	PANC-1	pancreas:	n/a
31	chr11:17300909-17300959	BJ	skin:	n/a
32	chr11:17300909-17300959	HMEC	breast:	n/a
33	chr11:17300909-17300959	GM12892	blood:	n/a
34	chr11:17300909-17300959	ovcar-3	ovarian:	n/a
35	chr11:17300909-17300959	SK-N-SH_RA	brain:	n/a
36	chr11:17300909-17300959	HCM	heart:	n/a
37	chr11:17300909-17300959	ProgFib	skin:	n/a
38	chr11:17300909-17300959	AG10803	skin:	n/a
39	chr11:17300909-17300959	HRE	kidney:	n/a
40	chr11:17300909-17300959	BE2_C	brain:	n/a
41	chr11:17300909-17300959	HUVEC	blood vessel:	n/a
42	chr11:17300909-17300959	NB4	blood:	n/a
43	chr11:17300909-17300959	HepG2	liver:	n/a
44	chr11:17300909-17300959	AG09309	skin:	n/a
45	chr11:17300909-17300959	RPTEC	kidney:	n/a
46	chr11:17300909-17300959	HNPCEpiC	eye:	n/a
47	chr11:17300909-17300959	HEEpiC	esophagus:	n/a
48	chr11:17300909-17300959	HCT-116	colon:	n/a
49	chr11:17300909-17300959	AoSMC	blood vessel:	n/a
50	chr11:17300909-17300959	HCF	heart:	n/a

(count:15 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:17297082..17301177-chr11:17313853..17317788,6	K562	blood:
2	chr11:17308283..17309860-chr11:17310824..17312984,2	K562	blood:
3	chr11:17300662..17302728-chr11:17307021..17310347,3	K562	blood:
4	chr11:17296529..17299421-chr11:17301500..17303584,3	K562	blood:
5	chr11:17308283..17309860-chr11:17310824..17312984,2	K562	blood:
6	chr11:17305212..17308146-chr11:17308901..17311776,2	K562	blood:
7	chr11:17300662..17302728-chr11:17307021..17310347,3	K562	blood:
8	chr11:17297839..17299498-chr11:17314289..17315941,2	K562	blood:
9	chr11:17312629..17314667-chr11:17373506..17375869,2	K562	blood:
10	chr11:17297082..17301177-chr11:17313853..17317788,6	K562	blood:
11	chr11:17293894..17295404-chr11:17299540..17302043,2	K562	blood:
12	chr11:17298938..17303193-chr11:17304940..17310347,8	K562	blood:
13	chr11:17289797..17291811-chr11:17310885..17313618,2	MCF-7	breast:
14	chr11:17298938..17303193-chr11:17304940..17310347,8	K562	blood:
15	chr11:17305212..17308146-chr11:17308901..17311776,2	K562	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KCNJ11-5	chr11:17315881-17316560	l_439_chr11:17315763-17328093_testes
2	lnc-RP1-239B22.1.1-2	chr11:17304336-17304417	NONHSAT018222
3	lnc-KCNJ11-5	chr11:17315764-17315875	l_439_chr11:17315763-17328093_testes
4	lnc-RP1-239B22.1.1-2	chr11:17304337-17304490	NONHSAT018223

No data

Variant related genes	Relation type
NUCB2	TF binding region
NUCB2	CpG island
ENSG00000070081	chromatin interactions

Extended variants
information (count: 555 )
Associated
traits (count: 54 )

Variant overlapped rSNPs/rCNVs (count:555 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7127347	chr11:17300844-17300845	Weak transcription Enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs144524189	chr11:17300850-17300851	Weak transcription Enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs531129221	chr11:17300858-17300859	Weak transcription Enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs549061584	chr11:17300860-17300861	Weak transcription Enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs560860502	chr11:17300895-17300896	Weak transcription Enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs370025947	chr11:17300909-17300910	Weak transcription Enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs546307410	chr11:17300910-17300911	Weak transcription Enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs570935278	chr11:17300916-17300917	Weak transcription Enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs146594726	chr11:17300918-17300919	Weak transcription Enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs550473099	chr11:17300942-17300943	Weak transcription Enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs191266132	chr11:17300989-17300990	Weak transcription Enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs184724136	chr11:17301026-17301027	Weak transcription Enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs369445113	chr11:17301066-17301067	Weak transcription Enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs187567190	chr11:17301124-17301125	Weak transcription Enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs192165033	chr11:17301146-17301147	Weak transcription Enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs76387565	chr11:17301181-17301182	Weak transcription Enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
17	rs185062983	chr11:17301200-17301201	Weak transcription Enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
18	rs541434811	chr11:17301327-17301328	Weak transcription Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
19	rs565885946	chr11:17301347-17301348	Weak transcription Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
20	rs557999615	chr11:17301348-17301349	Weak transcription Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
21	rs397849437	chr11:17301349-17301350	Weak transcription Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
22	rs34261908	chr11:17301350-17301351	Weak transcription Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
23	rs111565502	chr11:17301439-17301440	Weak transcription Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
24	rs578077077	chr11:17301490-17301491	Weak transcription Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
25	rs35815322	chr11:17301532-17301533	Weak transcription Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs190161870	chr11:17301540-17301541	Weak transcription Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs564742201	chr11:17301577-17301578	Weak transcription Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs138002805	chr11:17301583-17301584	Weak transcription Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs575900880	chr11:17301653-17301654	Weak transcription Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs542887882	chr11:17301662-17301663	Weak transcription Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs561016663	chr11:17301680-17301681	Weak transcription Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs543820272	chr11:17301714-17301715	Weak transcription Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs528147554	chr11:17301785-17301786	Weak transcription Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs559790272	chr11:17301808-17301809	Weak transcription Enhancers Genic enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs373057403	chr11:17301809-17301810	Weak transcription Enhancers Genic enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs557319915	chr11:17301871-17301872	Weak transcription Enhancers Genic enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs377187912	chr11:17301879-17301880	Weak transcription Enhancers Genic enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs555463028	chr11:17301909-17301910	Weak transcription Enhancers Genic enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs531985909	chr11:17301910-17301911	Weak transcription Enhancers Genic enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs550449964	chr11:17301920-17301921	Weak transcription Enhancers Genic enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs568845939	chr11:17301923-17301924	Weak transcription Enhancers Genic enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs536422993	chr11:17301990-17301991	Weak transcription Enhancers Genic enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs6486360	chr11:17302046-17302047	Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs562606697	chr11:17302162-17302163	Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs143041207	chr11:17302230-17302231	Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs181420512	chr11:17302269-17302270	Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs184858387	chr11:17302299-17302300	Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs12794099	chr11:17302308-17302309	Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
49	rs575778214	chr11:17302356-17302357	Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs373786607	chr11:17302360-17302361	Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:54)

Disease	PMID	Source
Cancer	21183584	CNVD
Gastric adenocarcinoma	19115996	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	19759907	CNVD
Breast cancer	17603634	CNVD
Medulloblastoma	21979893	CNVD
Thyroid cancer	19087340	CNVD
Melanoma	18172304	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Wilms tumour	21544195	CNVD
Parathyroid adenoma	22454399	CNVD
Chordoma	21602918	CNVD
Breast cancer	21949216	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	19222835	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Beckwith-Wiedemann syndrome	21518781	CNVD
Wilms tumour	21518781	CNVD
Hepatoblastoma	21518781	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Gastric cancer	17908304	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Multiple myeloma	20724749	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
small cell lung cancer	20016488	CNVD
Autism	22495311	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Multiple myeloma	16461302	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	21858162	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	21785460	CNVD
Myelofibrosis	22110671	CNVD
Neuroblastoma	21899760	CNVD
Lung adenocarcinoma	17086460	CNVD
Urothelial cell carcinoma	18451213	CNVD
Lung cancer	17086460	CNVD
Uterine serous papillary cancer	19536090	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:456 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:17298000-17301200	Active TSS	Primary T killer naive cells fromperipheralblood	blood
2	chr11:17298000-17302000	Active TSS	Thymus	Thymus
3	chr11:17299000-17301000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
4	chr11:17299000-17301400	Weak transcription	Pancreas	Pancrea
5	chr11:17299000-17301600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr11:17299000-17302200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr11:17299000-17307200	Weak transcription	Left Ventricle	heart
8	chr11:17299000-17307400	Weak transcription	Sigmoid Colon	Sigmoid Colon
9	chr11:17299000-17307600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr11:17299000-17307600	Weak transcription	Fetal Muscle Trunk	muscle
11	chr11:17299000-17307600	Weak transcription	Lung	lung
12	chr11:17299000-17316200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
13	chr11:17299000-17320000	Weak transcription	Esophagus	oesophagus
14	chr11:17299000-17323200	Weak transcription	Ovary	ovary
15	chr11:17299000-17323400	Weak transcription	Aorta	Aorta
16	chr11:17299000-17357200	Weak transcription	Placenta Amnion	Placenta Amnion
17	chr11:17299000-17357600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
18	chr11:17299000-17360600	Weak transcription	Small Intestine	intestine
19	chr11:17299200-17301400	Weak transcription	Skeletal Muscle Female	skeletal muscle
20	chr11:17299200-17301400	Weak transcription	Stomach Mucosa	stomach
21	chr11:17299200-17301800	Weak transcription	Primary monocytes fromperipheralblood	blood
22	chr11:17299200-17302200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
23	chr11:17299200-17302200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
24	chr11:17299200-17302400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
25	chr11:17299200-17305600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
26	chr11:17299200-17305600	Weak transcription	Fetal Stomach	stomach
27	chr11:17299200-17306000	Weak transcription	Placenta	Placenta
28	chr11:17299200-17307400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
29	chr11:17299200-17307400	Weak transcription	Fetal Muscle Leg	muscle
30	chr11:17299200-17307600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
31	chr11:17299200-17307600	Weak transcription	Psoas Muscle	Psoas
32	chr11:17299200-17307600	Weak transcription	Rectal Smooth Muscle	rectum
33	chr11:17299200-17307600	Weak transcription	Skeletal Muscle Male	skeletal muscle
34	chr11:17299200-17310400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
35	chr11:17299200-17317800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
36	chr11:17299200-17317800	Weak transcription	Right Ventricle	heart
37	chr11:17299200-17319800	Weak transcription	Fetal Intestine Small	intestine
38	chr11:17299200-17325600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
39	chr11:17299200-17329600	Weak transcription	Brain Hippocampus Middle	brain
40	chr11:17299200-17357000	Weak transcription	Brain Substantia Nigra	brain
41	chr11:17299400-17301000	Enhancers	Primary T killer memory cells from peripheral blood	blood
42	chr11:17299400-17301200	Weak transcription	NHEK	skin
43	chr11:17299400-17301400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
44	chr11:17299400-17301600	Enhancers	Fetal Heart	heart
45	chr11:17299400-17301800	Weak transcription	HepG2	liver
46	chr11:17299400-17304400	Weak transcription	Fetal Lung	lung
47	chr11:17299400-17304600	Weak transcription	Adipose Nuclei	Adipose
48	chr11:17299400-17304600	Weak transcription	Colon Smooth Muscle	Colon
49	chr11:17299400-17304800	Weak transcription	Liver	Liver
50	chr11:17299400-17304800	Weak transcription	Brain Anterior Caudate	brain

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