Variant report

Variant	nsv825873
Chromosome Location	chr11:47609306-47616463
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:85)
CpG islands
(count:611)
Chromatin interactive
region (count:8)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:85 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CHD1	chr11:47615782-47615878	H1-hESC	embryonic stem cell:	n/a	n/a
2	CHD2	chr11:47615933-47615976	H1-hESC	embryonic stem cell:	n/a	n/a
3	CTBP2	chr11:47615005-47616353	H1-hESC	embryonic stem cell:	n/a	n/a
4	CTCF	chr11:47612188-47612296	H1-hESC	embryonic stem cell:	n/a	n/a
5	CTCF	chr11:47616460-47616610	Hela-S3	cervix:	n/a	n/a
6	CTCF	chr11:47611840-47611990	HUVEC	blood vessel:	n/a	n/a
7	EGR1	chr11:47609242-47609407	K562	blood:	n/a	n/a
8	EGR1	chr11:47609193-47609373	K562	blood:	n/a	n/a
9	ELF1	chr11:47609136-47609857	HepG2	liver:	n/a	n/a
10	ELF1	chr11:47609147-47609441	HepG2	liver:	n/a	n/a
11	GABPA	chr11:47609219-47609562	HepG2	liver:	n/a	n/a
12	GABPA	chr11:47609224-47609742	HepG2	liver:	n/a	n/a
13	HEY1	chr11:47609152-47609437	HepG2	liver:	n/a	n/a
14	HEY1	chr11:47609123-47609921	HepG2	liver:	n/a	n/a
15	HEY1	chr11:47609568-47609948	HepG2	liver:	n/a	n/a
16	HNF4A	chr11:47609599-47609982	HepG2	liver:	n/a	n/a
17	HNF4G	chr11:47609563-47609945	HepG2	liver:	n/a	chr11:47609780-47609795
18	JUN	chr11:47610939-47610953	HepG2	liver:	n/a	n/a
19	MAX	chr11:47609051-47610061	HepG2	liver:	n/a	chr11:47609697-47609707
20	MAX	chr11:47611189-47611881	HUVEC	blood vessel:	n/a	n/a
21	MAX	chr11:47609591-47609707	K562	blood:	n/a	chr11:47609697-47609707
22	MAX	chr11:47609579-47609880	HepG2	liver:	n/a	chr11:47609697-47609707
23	MAX	chr11:47608775-47609985	NB4	blood:	n/a	chr11:47609697-47609707
24	MAX	chr11:47613221-47614234	NB4	blood:	n/a	chr11:47614159-47614172 chr11:47614161-47614170 chr11:47614160-47614171 chr11:47614160-47614171 chr11:47614160-47614170 chr11:47614159-47614172
25	MAZ	chr11:47609407-47609548	HepG2	liver:	n/a	n/a
26	MTA3	chr11:47613194-47613699	GM12878	blood:	n/a	n/a
27	MYBL2	chr11:47613290-47613705	HepG2	liver:	n/a	chr11:47613491-47613501
28	MYBL2	chr11:47609144-47609594	HepG2	liver:	n/a	n/a
29	MYC	chr11:47613239-47613892	NB4	blood:	n/a	n/a
30	MYC	chr11:47609276-47609409	HepG2	liver:	n/a	n/a
31	MYC	chr11:47611462-47611680	HUVEC	blood vessel:	n/a	n/a
32	MYC	chr11:47611687-47611728	HUVEC	blood vessel:	n/a	n/a
33	MYC	chr11:47611944-47611951	HUVEC	blood vessel:	n/a	n/a
34	MYC	chr11:47609113-47610308	NB4	blood:	n/a	chr11:47609697-47609707
35	MYC	chr11:47609471-47609795	HepG2	liver:	n/a	chr11:47609697-47609707
36	NFE2	chr11:47614824-47614869	GM12878	blood:	n/a	n/a
37	NRF1	chr11:47615939-47616062	H1-hESC	embryonic stem cell:	n/a	n/a
38	NRF1	chr11:47611795-47611856	H1-hESC	embryonic stem cell:	n/a	n/a
39	POLR2A	chr11:47609544-47609903	HepG2	liver:	n/a	n/a
40	POLR2A	chr11:47609055-47609979	NB4	blood:	n/a	n/a
41	POLR2A	chr11:47609386-47609995	HL-60	blood:	n/a	n/a
42	POLR2A	chr11:47611206-47612092	HUVEC	blood vessel:	n/a	n/a
43	POLR2A	chr11:47611892-47612100	HUVEC	blood vessel:	n/a	n/a
44	POLR2A	chr11:47609216-47609537	HepG2	liver:	n/a	n/a
45	POLR2A	chr11:47611383-47612047	HUVEC	blood vessel:	n/a	n/a
46	POLR2A	chr11:47609348-47609980	HL-60	blood:	n/a	n/a
47	POLR2A	chr11:47615907-47616249	H1-hESC	embryonic stem cell:	n/a	n/a
48	POLR2A	chr11:47613439-47613699	HUVEC	blood vessel:	n/a	n/a
49	POLR2A	chr11:47611682-47611879	HUVEC	blood vessel:	n/a	n/a
50	POLR2A	chr11:47609175-47609855	HepG2	liver:	n/a	n/a

(count:611 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:47610098-47610148	PFSK-1	brain:	n/a
2	chr11:47610098-47610148	PFSK-1	brain:	n/a
3	chr11:47611780-47611830	A549	lung:	n/a
4	chr11:47615333-47615383	Caco-2	colon:	n/a
5	chr11:47609357-47609407	MCF10A-Er-Src	breast:	n/a
6	chr11:47612070-47612120	GM12891	blood:	n/a
7	chr11:47609357-47609407	HepG2	liver:	n/a
8	chr11:47612070-47612120	GM06990	blood:	n/a
9	chr11:47612070-47612120	Jurkat	blood:	n/a
10	chr11:47612070-47612120	SK-N-SH_RA	brain:	n/a
11	chr11:47609357-47609407	HEK293	kidney:	embryo
12	chr11:47612070-47612120	SK-N-SH	brain:	n/a
13	chr11:47615333-47615383	HEEpiC	esophagus:	n/a
14	chr11:47615333-47615383	Hepatocyte	liver:	n/a
15	chr11:47611780-47611830	IMR90	lung:	fetal
16	chr11:47615333-47615383	HUVEC	blood vessel:	n/a
17	chr11:47615898-47615948	NH-A	brain:	n/a
18	chr11:47612070-47612120	PrEC	prostate:	n/a
19	chr11:47611236-47611286	GM12892	blood:	n/a
20	chr11:47613458-47613508	A549	lung:	n/a
21	chr11:47613458-47613508	AG04450	lung:	fetal
22	chr11:47615333-47615383	MCF10A-Er-Src	breast:	n/a
23	chr11:47615898-47615948	AG04450	lung:	fetal
24	chr11:47613458-47613508	PFSK-1	brain:	n/a
25	chr11:47609357-47609407	T-47D	breast:	n/a
26	chr11:47615898-47615948	NHDF-neo	bronchial:	n/a
27	chr11:47613458-47613508	SKMC	muscle:	n/a
28	chr11:47609357-47609407	NHBE	bronchial:	n/a
29	chr11:47613458-47613508	SAEC	small airway:	n/a
30	chr11:47613458-47613508	GM12891	blood:	n/a
31	chr11:47615333-47615383	U87	brain:	n/a
32	chr11:47612380-47612430	NB4	blood:	n/a
33	chr11:47611236-47611286	NB4	blood:	n/a
34	chr11:47615898-47615948	HRCEpiC	kidney:	n/a
35	chr11:47616096-47616146	AoSMC	blood vessel:	n/a
36	chr11:47610098-47610148	MCF-7	breast:	n/a
37	chr11:47612070-47612120	ProgFib	skin:	n/a
38	chr11:47611236-47611286	GM12891	blood:	n/a
39	chr11:47612380-47612430	Hepatocyte	liver:	n/a
40	chr11:47613458-47613508	K562	blood:	n/a
41	chr11:47613458-47613508	SK-N-SH_RA	brain:	n/a
42	chr11:47612380-47612430	ProgFib	skin:	n/a
43	chr11:47613458-47613508	H1-hESC	embryonic stem cell:	embryo
44	chr11:47611780-47611830	LNCaP	prostate:	n/a
45	chr11:47609357-47609407	MCF-7	breast:	n/a
46	chr11:47609357-47609407	HCPEpiC	choroid plexus:	n/a
47	chr11:47612070-47612120	AG04449	skin:	fetal
48	chr11:47611236-47611286	HEEpiC	esophagus:	n/a
49	chr11:47615898-47615948	T-47D	breast:	n/a
50	chr11:47613458-47613508	HCF	heart:	n/a

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:47613544..47615870-chr11:47616778..47619516,2	K562	blood:
2	chr11:47586403..47589804-chr11:47615450..47617603,3	MCF-7	breast:
3	chr11:47586895..47590126-chr11:47609798..47613644,4	MCF-7	breast:
4	chr11:47573328..47575727-chr11:47613436..47615022,2	MCF-7	breast:
5	chr11:47609240..47610028-chr11:69259601..69260202,2	NB4	blood:
6	chr11:47612536..47615119-chr11:47621366..47624044,3	MCF-7	breast:
7	chr11:47612748..47614519-chr11:47788847..47791684,2	K562	blood:
8	chr11:47612835..47615053-chr11:47623359..47624985,2	MCF-7	breast:

No data

Variant related genes	Relation type
C1QTNF4	TF binding region
C1QTNF4	CpG island
ENSG00000213619	chromatin interactions
ENSG00000110536	chromatin interactions
ENSG00000149187	chromatin interactions
ENSG00000109920	chromatin interactions

Extended variants
information (count: 266 )
Associated
traits (count: 63 )

Variant overlapped rSNPs/rCNVs (count:266 , 50 per page) page: 1 2 3 4 5 6

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs368443858	chr11:47609306-47609307	Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Strong transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs372385787	chr11:47609312-47609313	Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Strong transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs141304714	chr11:47609321-47609322	Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Strong transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs573408568	chr11:47609337-47609338	Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Strong transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs368745483	chr11:47609347-47609348	Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Strong transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs567391483	chr11:47609352-47609353	Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Strong transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs535945744	chr11:47609357-47609358	Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Strong transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs546647243	chr11:47609358-47609359	Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Strong transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs567086871	chr11:47609371-47609372	Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Strong transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs539196776	chr11:47609373-47609374	Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Strong transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs78127409	chr11:47609397-47609398	Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Strong transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs575997804	chr11:47609406-47609407	Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Strong transcription Genic enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs538272330	chr11:47609419-47609420	Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Strong transcription Genic enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs554644844	chr11:47609441-47609442	Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Strong transcription Genic enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs541581357	chr11:47609500-47609501	Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Strong transcription Genic enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs376408223	chr11:47609656-47609657	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs574745132	chr11:47609660-47609661	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs368777210	chr11:47609672-47609673	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs373977217	chr11:47609673-47609674	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs540383221	chr11:47609675-47609676	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs560170516	chr11:47609704-47609705	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs572703009	chr11:47609739-47609740	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs544802542	chr11:47609754-47609755	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs376058507	chr11:47609818-47609819	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs186932505	chr11:47609819-47609820	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs373548103	chr11:47609820-47609821	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs191781208	chr11:47609826-47609827	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs376276491	chr11:47609856-47609857	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs184213461	chr11:47609866-47609867	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs4486587	chr11:47609867-47609868	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs546728298	chr11:47609900-47609901	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs566568495	chr11:47609937-47609938	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs532794522	chr11:47609964-47609965	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs190163835	chr11:47610007-47610008	Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Active TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs115468467	chr11:47610034-47610035	Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Active TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs190264387	chr11:47610043-47610044	Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Active TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs569599780	chr11:47610063-47610064	Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Active TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs577497965	chr11:47610071-47610072	Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Active TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs1040199	chr11:47610080-47610081	Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Active TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs78369932	chr11:47610098-47610099	Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Active TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs568370353	chr11:47610127-47610128	Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Active TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs375632808	chr11:47610207-47610208	Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Active TSS Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs181919228	chr11:47610229-47610230	Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Active TSS Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs571206210	chr11:47610236-47610237	Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Active TSS Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs146171408	chr11:47610269-47610270	Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Active TSS Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs149775746	chr11:47610271-47610272	Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Active TSS Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs55944090	chr11:47610272-47610273	Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Active TSS Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs5020951	chr11:47610273-47610274	Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Active TSS Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs201828486	chr11:47610275-47610276	Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Active TSS Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs149663299	chr11:47610277-47610278	Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Active TSS Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:63)

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
Renal cell carcinoma	18194544	CNVD
Breast cancer	17603634	CNVD
Chordoma	18071362	CNVD
T-cell prolymphocytic leukemia	19278963	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
Breast cancer	21364760	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
lymphocytic leukemia	21291569	CNVD
Obesity	20935630	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:698 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:47601400-47611800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr11:47601400-47613400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
3	chr11:47602200-47610400	Strong transcription	Fetal Brain Female	brain
4	chr11:47602400-47609800	Strong transcription	Fetal Stomach	stomach
5	chr11:47602600-47610000	Strong transcription	Brain Germinal Matrix	brain
6	chr11:47603800-47612400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
7	chr11:47604000-47612000	Weak transcription	Small Intestine	intestine
8	chr11:47604400-47610800	Weak transcription	Pancreatic Islets	Pancreatic Islet
9	chr11:47605000-47611000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr11:47605600-47610800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
11	chr11:47605800-47610200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
12	chr11:47605800-47610200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
13	chr11:47605800-47610200	Weak transcription	Fetal Kidney	kidney
14	chr11:47605800-47610800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
15	chr11:47606000-47610400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
16	chr11:47606000-47611000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
17	chr11:47606000-47611400	Weak transcription	HMEC	breast
18	chr11:47606000-47614200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr11:47606200-47609400	Weak transcription	Muscle Satellite Cultured Cells	--
20	chr11:47606200-47610200	Weak transcription	Colon Smooth Muscle	Colon
21	chr11:47606200-47610800	Weak transcription	Fetal Heart	heart
22	chr11:47606200-47610800	Weak transcription	Rectal Mucosa Donor 31	rectum
23	chr11:47606200-47611200	Weak transcription	Colonic Mucosa	Colon
24	chr11:47606200-47611400	Weak transcription	NH-A	brain
25	chr11:47606200-47612000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
26	chr11:47606200-47612600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
27	chr11:47606200-47614200	Weak transcription	A549	lung
28	chr11:47606200-47614600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
29	chr11:47606400-47610600	Weak transcription	NHEK	skin
30	chr11:47606400-47610600	Weak transcription	Osteobl	bone
31	chr11:47606400-47612000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
32	chr11:47606400-47612400	Weak transcription	GM12878-XiMat	blood
33	chr11:47606600-47613400	Weak transcription	Primary T helper cells PMA-I stimulated	--
34	chr11:47606800-47610000	Weak transcription	Duodenum Smooth Muscle	Duodenum
35	chr11:47606800-47610800	Weak transcription	HUVEC	blood vessel
36	chr11:47606800-47611400	Weak transcription	Gastric	stomach
37	chr11:47606800-47611600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
38	chr11:47606800-47613200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr11:47606800-47613600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
40	chr11:47606800-47613600	Weak transcription	HUES64 Cell Line	embryonic stem cell
41	chr11:47607000-47609400	Weak transcription	Primary neutrophils fromperipheralblood	blood
42	chr11:47607000-47609600	Weak transcription	Liver	Liver
43	chr11:47607000-47610200	Weak transcription	Ovary	ovary
44	chr11:47607000-47610600	Weak transcription	Fetal Lung	lung
45	chr11:47607000-47610600	Weak transcription	Placenta Amnion	Placenta Amnion
46	chr11:47607000-47610800	Weak transcription	Rectal Smooth Muscle	rectum
47	chr11:47607000-47611000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
48	chr11:47607000-47611000	Weak transcription	Left Ventricle	heart
49	chr11:47607000-47611200	Weak transcription	Psoas Muscle	Psoas
50	chr11:47607000-47611600	Weak transcription	HUES48 Cell Line	embryonic stem cell

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