Variant report

Variant	nsv522319
Chromosome Location	chr1:47080741-47094267
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:598)
CpG islands
(count:732)
Chromatin interactive
region (count:20)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:598 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:47081854-47082029	K562	blood:	n/a	n/a
2	ARID3A	chr1:47082602-47082884	K562	blood:	n/a	n/a
3	ARID3A	chr1:47083799-47084297	HepG2	liver:	n/a	n/a
4	ATF3	chr1:47082190-47082462	K562	blood:	n/a	n/a
5	BACH1	chr1:47081911-47082740	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr1:47082703-47082950	K562	blood:	n/a	n/a
7	BACH1	chr1:47081522-47081670	H1-hESC	embryonic stem cell:	n/a	n/a
8	BCL3	chr1:47082395-47083126	A549	lung:	n/a	n/a
9	BCLAF1	chr1:47082163-47082843	GM12878	blood:	n/a	n/a
10	BHLHE40	chr1:47081937-47082856	GM12878	blood:	n/a	n/a
11	BHLHE40	chr1:47081880-47083091	K562	blood:	n/a	n/a
12	BRCA1	chr1:47082270-47082469	GM12878	blood:	n/a	n/a
13	BRCA1	chr1:47088192-47088410	Hela-S3	cervix:	n/a	n/a
14	CBX3	chr1:47081882-47082932	K562	blood:	n/a	n/a
15	CCNT2	chr1:47082223-47082697	K562	blood:	n/a	n/a
16	CCNT2	chr1:47089446-47089747	K562	blood:	n/a	n/a
17	CEBPB	chr1:47083704-47083921	HepG2	liver:	n/a	n/a
18	CEBPB	chr1:47088083-47088454	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr1:47081297-47081367	HepG2	liver:	n/a	n/a
20	CEBPD	chr1:47082181-47082773	HepG2	liver:	n/a	n/a
21	CHD1	chr1:47082219-47082764	GM12878	blood:	n/a	n/a
22	CHD2	chr1:47081678-47081985	Hela-S3	cervix:	n/a	n/a
23	CHD2	chr1:47082238-47082622	K562	blood:	n/a	n/a
24	CHD2	chr1:47082377-47083011	Hela-S3	cervix:	n/a	n/a
25	CHD2	chr1:47081788-47081989	K562	blood:	n/a	n/a
26	CHD2	chr1:47081354-47082855	GM12878	blood:	n/a	n/a
27	CREB1	chr1:47081818-47082900	GM12878	blood:	n/a	n/a
28	CREB1	chr1:47081935-47082163	A549	lung:	n/a	n/a
29	CREB1	chr1:47082343-47082926	A549	lung:	n/a	n/a
30	CTBP2	chr1:47081874-47083178	H1-hESC	embryonic stem cell:	n/a	n/a
31	CTCF	chr1:47088106-47088530	K562	blood:	n/a	n/a
32	CTCF	chr1:47088240-47088390	HCM	heart:	n/a	n/a
33	CTCF	chr1:47088260-47088410	Hela-S3	cervix:	n/a	n/a
34	CTCF	chr1:47088218-47088436	MCF-7	breast:	n/a	n/a
35	CTCF	chr1:47088280-47088430	GM12878	blood:	n/a	n/a
36	CTCF	chr1:47088280-47088430	K562	blood:	n/a	n/a
37	CTCF	chr1:47088199-47088417	ECC-1	luminal epithelium:	n/a	n/a
38	CTCF	chr1:47088202-47088451	NHEK	skin:	n/a	n/a
39	CTCF	chr1:47088240-47088390	HRPEpiC	eye:	n/a	n/a
40	CTCF	chr1:47088260-47088410	HFF-Myc	foreskin:	n/a	n/a
41	CTCF	chr1:47088223-47088436	MCF-7	breast:	n/a	n/a
42	CTCF	chr1:47088240-47088390	GM12865	blood:	n/a	n/a
43	CTCF	chr1:47088222-47088450	HepG2	liver:	n/a	n/a
44	CTCF	chr1:47088245-47088419	MCF-7	breast:	n/a	n/a
45	CTCF	chr1:47088280-47088430	HPF	lung:	n/a	n/a
46	CTCF	chr1:47082220-47082370	HCPEpiC	choroid plexus:	n/a	n/a
47	CTCF	chr1:47086100-47086250	HepG2	liver:	n/a	n/a
48	CTCF	chr1:47088172-47088457	HepG2	liver:	n/a	n/a
49	CTCF	chr1:47088260-47088410	HCFaa	heart:	n/a	n/a
50	CTCF	chr1:47088097-47088514	H1-hESC	embryonic stem cell:	n/a	n/a

(count:732 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:47082869-47082919	A549	lung:	n/a
2	chr1:47082372-47082422	SK-N-MC	brain:	n/a
3	chr1:47082211-47082261	Jurkat	blood:	n/a
4	chr1:47082037-47082087	K562	blood:	n/a
5	chr1:47082211-47082261	HCF	heart:	n/a
6	chr1:47082039-47082089	GM06990	blood:	n/a
7	chr1:47082372-47082422	HPAEpiC	pulmonary alveolar:	n/a
8	chr1:47082039-47082089	K562	blood:	n/a
9	chr1:47081524-47081574	HCM	heart:	n/a
10	chr1:47082039-47082089	ovcar-3	ovarian:	n/a
11	chr1:47082372-47082422	GM12878	blood:	n/a
12	chr1:47086491-47086541	HCM	heart:	n/a
13	chr1:47082372-47082422	PrEC	prostate:	n/a
14	chr1:47082039-47082089	NHBE	bronchial:	n/a
15	chr1:47082831-47082881	HPAEpiC	pulmonary alveolar:	n/a
16	chr1:47082129-47082179	HCPEpiC	choroid plexus:	n/a
17	chr1:47081524-47081574	GM12891	blood:	n/a
18	chr1:47082129-47082179	CMK	blood:	n/a
19	chr1:47082767-47082817	AG09309	skin:	n/a
20	chr1:47082851-47082901	HEK293	kidney:	embryo
21	chr1:47082037-47082087	HCM	heart:	n/a
22	chr1:47082691-47082741	GM12878	blood:	n/a
23	chr1:47082851-47082901	HRCEpiC	kidney:	n/a
24	chr1:47082037-47082087	HRCEpiC	kidney:	n/a
25	chr1:47082767-47082817	HCM	heart:	n/a
26	chr1:47086491-47086541	HPAEpiC	pulmonary alveolar:	n/a
27	chr1:47082372-47082422	A549	lung:	n/a
28	chr1:47082037-47082087	NHBE	bronchial:	n/a
29	chr1:47082691-47082741	HRE	kidney:	n/a
30	chr1:47082767-47082817	NH-A	brain:	n/a
31	chr1:47082767-47082817	GM12892	blood:	n/a
32	chr1:47082767-47082817	SK-N-SH_RA	brain:	n/a
33	chr1:47082851-47082901	LNCaP	prostate:	n/a
34	chr1:47082039-47082089	LNCaP	prostate:	n/a
35	chr1:47082851-47082901	ProgFib	skin:	n/a
36	chr1:47082037-47082087	HUVEC	blood vessel:	n/a
37	chr1:47082831-47082881	HCM	heart:	n/a
38	chr1:47082211-47082261	Caco-2	colon:	n/a
39	chr1:47082851-47082901	BJ	skin:	n/a
40	chr1:47082129-47082179	BJ	skin:	n/a
41	chr1:47082691-47082741	HCPEpiC	choroid plexus:	n/a
42	chr1:47082372-47082422	AG04450	lung:	fetal
43	chr1:47082372-47082422	HEEpiC	esophagus:	n/a
44	chr1:47082211-47082261	HUVEC	blood vessel:	n/a
45	chr1:47082767-47082817	AoSMC	blood vessel:	n/a
46	chr1:47082039-47082089	PANC-1	pancreas:	n/a
47	chr1:47086491-47086541	HCF	heart:	n/a
48	chr1:47082691-47082741	AG10803	skin:	n/a
49	chr1:47082039-47082089	HCT-116	colon:	n/a
50	chr1:47082129-47082179	HepG2	liver:	n/a

(count:20 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:47077660..47081751-chr1:47132686..47135354,3	MCF-7	breast:
2	chr1:47080724..47082396-chr1:47183672..47185631,2	MCF-7	breast:
3	chr1:47080354..47082092-chr1:47110886..47112430,2	MCF-7	breast:
4	chr1:47079661..47082285-chr1:47135813..47137705,2	K562	blood:
5	chr1:47078421..47080865-chr1:47080975..47083544,2	MCF-7	breast:
6	chr1:47088932..47089596-chr1:47190617..47191353,2	MCF-7	breast:
7	chr1:47087818..47089652-chr1:47106481..47108594,2	MCF-7	breast:
8	chr1:47069390..47072755-chr1:47079314..47082367,4	MCF-7	breast:
9	chr1:47086033..47090385-chr1:47091411..47095597,5	K562	blood:
10	chr1:47089433..47091250-chr1:47102705..47105351,2	K562	blood:
11	chr1:47068429..47072503-chr1:47081068..47085092,4	MCF-7	breast:
12	chr1:47087714..47088829-chr1:47190613..47191839,11	K562	blood:
13	chr1:47078421..47080865-chr1:47080975..47083544,2	MCF-7	breast:
14	chr1:47091302..47093763-chr1:47181587..47183697,2	K562	blood:
15	chr1:47081490..47084087-chr1:47086263..47088090,2	MCF-7	breast:
16	chr1:47090932..47093400-chr1:47190525..47192623,2	MCF-7	breast:
17	chr1:47073700..47076420-chr1:47091166..47093080,2	K562	blood:
18	chr1:47086033..47090385-chr1:47091411..47095597,5	K562	blood:
19	chr1:47087884..47088399-chr1:47191014..47191583,2	MCF-7	breast:
20	chr1:47093097..47096139-chr1:47100393..47103970,3	K562	blood:

No data

Variant related genes	Relation type
MKNK1	TF binding region
MOB3C	TF binding region
MKNK1	CpG island
MOB3C	CpG island
ENSG00000079277	chromatin interactions
ENSG00000186118	chromatin interactions
ENSG00000159658	chromatin interactions
ENSG00000123472	chromatin interactions
ENSG00000142961	chromatin interactions

Extended variants
information (count: 516 )
Associated
traits (count: 89 )

Variant overlapped rSNPs/rCNVs (count:516 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12029680	chr1:47080741-47080742	Enhancers Weak transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs149129109	chr1:47080749-47080750	Enhancers Weak transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
3	rs563591134	chr1:47080754-47080755	Enhancers Weak transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
4	rs373454329	chr1:47080780-47080781	Enhancers Weak transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
5	rs531129868	chr1:47080789-47080790	Enhancers Weak transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
6	rs150683373	chr1:47080911-47080912	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
7	rs374623875	chr1:47080956-47080957	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
8	rs549517813	chr1:47080968-47080969	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
9	rs7415243	chr1:47080972-47080973	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
10	rs35494693	chr1:47080983-47080984	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs181530264	chr1:47081034-47081035	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
12	rs111464029	chr1:47081070-47081071	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
13	rs372663879	chr1:47081112-47081113	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
14	rs80159866	chr1:47081119-47081120	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
15	rs6681420	chr1:47081137-47081138	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs117603111	chr1:47081157-47081158	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
17	rs147890167	chr1:47081199-47081200	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
18	rs560258535	chr1:47081254-47081255	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
19	rs141654491	chr1:47081274-47081275	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
20	rs147085297	chr1:47081334-47081335	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
21	rs541260679	chr1:47081364-47081365	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
22	rs559380235	chr1:47081372-47081373	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
23	rs187063957	chr1:47081378-47081379	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
24	rs371215352	chr1:47081517-47081518	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
25	rs551193080	chr1:47081525-47081526	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
26	rs191715717	chr1:47081566-47081567	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
27	rs113524643	chr1:47081624-47081625	Active TSS Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
28	rs563354715	chr1:47081630-47081631	Active TSS Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
29	rs530966895	chr1:47081650-47081651	Active TSS Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
30	rs549386409	chr1:47081723-47081724	Active TSS Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
31	rs112840680	chr1:47081746-47081747	Active TSS Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
32	rs183196731	chr1:47081752-47081753	Active TSS Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
33	rs114160720	chr1:47081772-47081773	Active TSS Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
34	rs113830724	chr1:47081815-47081816	Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
35	rs138510143	chr1:47081868-47081869	Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
36	rs551536547	chr1:47081886-47081887	Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
37	rs569529685	chr1:47081928-47081929	Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
38	rs28642145	chr1:47081971-47081972	Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
39	rs537096784	chr1:47081982-47081983	Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
40	rs377010737	chr1:47082013-47082014	Bivalent/Poised TSS Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
41	rs369448769	chr1:47082065-47082066	Bivalent/Poised TSS Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
42	rs112918665	chr1:47082079-47082080	Bivalent/Poised TSS Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
43	rs567560787	chr1:47082098-47082099	Bivalent/Poised TSS Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
44	rs537773133	chr1:47082101-47082102	Bivalent/Poised TSS Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
45	rs534469862	chr1:47082117-47082118	Bivalent/Poised TSS Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
46	rs386630905	chr1:47082136-47082137	Bivalent/Poised TSS Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
47	rs189528964	chr1:47082137-47082138	Bivalent/Poised TSS Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
48	rs545080649	chr1:47082181-47082182	Bivalent/Poised TSS Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
49	rs377104913	chr1:47082195-47082196	Bivalent/Poised TSS Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
50	rs79038044	chr1:47082211-47082212	Bivalent/Poised TSS Weak transcription Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:89)

Disease	PMID	Source
Glioblastoma multiforme	21080181	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	17603634	CNVD
Soft tissue tumor	16732325	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Colorectal cancer	16272173	CNVD
Wilms tumour	21544195	CNVD
Coronary Disease	20032323	CNVD
Prostate cancer	21965145	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Stargardt''s disease	17277736	CNVD
Neuroblastoma	17897457	CNVD
Uveal melanoma	21693616	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-syndromic sensorineural hearing loss	22290220	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	21264507	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	17387387	CNVD
Oligodendroglial tumors	17285580	CNVD
Neuroblastoma	17535989	CNVD
Pheochromocytoma	17535989	CNVD
Prostate cancer	16705090	CNVD
Astrocytoma	17934521	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Neuroblastoma	17533364	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Chronic myeloid leukemia	21384125	CNVD
Prostate cancer	18632612	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21385341	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Chordoma	21602918	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Melanoma	18172304	CNVD
Multiple myeloma	16461302	CNVD
Melanoma	17363583	CNVD
Cancer	21129771	CNVD
Autosomal dominant nocturnal frontal lobe epilepsy	18472482	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thrombocytopenia-absent radius syndrome	21933853	CNVD
Psychiatric disorder	22848183	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	20409316	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Muscle-eye-brain disease	21572526	CNVD
Breast cancer	21785460	CNVD
Myelofibrosis	22110671	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD
Neuroblastoma	21899760	CNVD
Uveal melanoma	20484589	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Glioblastoma	20031968	CNVD
Leukemia	18688285	CNVD
Rett syndrome	21593744	CNVD

Chromatin state (count:838 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:47070400-47081200	Weak transcription	Fetal Brain Male	brain
2	chr1:47076400-47081400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr1:47076800-47081800	Enhancers	H1 Cell Line	embryonic stem cell
4	chr1:47077000-47081000	Enhancers	Primary T killer memory cells from peripheral blood	blood
5	chr1:47077000-47081000	Enhancers	Brain Anterior Caudate	brain
6	chr1:47077000-47081200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
7	chr1:47077000-47081400	Enhancers	Left Ventricle	heart
8	chr1:47077000-47081400	Enhancers	Psoas Muscle	Psoas
9	chr1:47077000-47081600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr1:47077000-47082000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
11	chr1:47077200-47081200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
12	chr1:47077200-47081600	Enhancers	ES-I3 Cell Line	embryonic stem cell
13	chr1:47077400-47081200	Enhancers	HMEC	breast
14	chr1:47077600-47081600	Enhancers	Fetal Heart	heart
15	chr1:47078000-47081000	Enhancers	Hela-S3	cervix
16	chr1:47078000-47081400	Weak transcription	HUVEC	blood vessel
17	chr1:47078400-47081600	Enhancers	H9 Cell Line	embryonic stem cell
18	chr1:47078600-47081000	Enhancers	Primary T helper cells PMA-I stimulated	--
19	chr1:47078600-47081200	Enhancers	iPS-20b Cell Line	embryonic stem cell
20	chr1:47078800-47081200	Enhancers	Primary B cells from cord blood	blood
21	chr1:47078800-47081200	Enhancers	Primary T cells fromperipheralblood	blood
22	chr1:47078800-47081200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
23	chr1:47078800-47081200	Enhancers	Rectal Mucosa Donor 31	rectum
24	chr1:47078800-47081400	Enhancers	Primary hematopoietic stem cells	blood
25	chr1:47078800-47081800	Enhancers	Spleen	Spleen
26	chr1:47079000-47080800	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
27	chr1:47079000-47081000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
28	chr1:47079000-47081000	Enhancers	Primary T helper naive cells from peripheral blood	blood
29	chr1:47079000-47081000	Enhancers	NHDF-Ad	bronchial
30	chr1:47079000-47081200	Enhancers	Aorta	Aorta
31	chr1:47079000-47081200	Enhancers	Liver	Liver
32	chr1:47079000-47081200	Enhancers	Fetal Lung	lung
33	chr1:47079000-47081400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
34	chr1:47079000-47081400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
35	chr1:47079000-47081400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
36	chr1:47079000-47081400	Enhancers	Gastric	stomach
37	chr1:47079000-47081400	Enhancers	Stomach Mucosa	stomach
38	chr1:47079000-47081600	Enhancers	Cortex derived primary cultured neurospheres	brain
39	chr1:47079000-47082000	Flanking Active TSS	Adipose Nuclei	Adipose
40	chr1:47079000-47082000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
41	chr1:47079200-47081000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
42	chr1:47079200-47081000	Enhancers	Primary T cells from cord blood	blood
43	chr1:47079200-47081000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
44	chr1:47079200-47081000	Enhancers	Placenta	Placenta
45	chr1:47079200-47081000	Enhancers	NHLF	lung
46	chr1:47079200-47081200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
47	chr1:47079200-47081200	Enhancers	Dnd41	blood
48	chr1:47079200-47081200	Enhancers	HSMMtube	muscle
49	chr1:47079200-47081400	Enhancers	Esophagus	oesophagus
50	chr1:47079200-47081400	Enhancers	Lung	lung

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