Variant report

Variant	nsv870392
Chromosome Location	chr1:47040676-47095097
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1424)
CpG islands
(count:2201)
Chromatin interactive
region (count:74)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1424 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:47045945-47046419	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:47069705-47070171	HepG2	liver:	n/a	n/a
3	ARID3A	chr1:47082602-47082884	K562	blood:	n/a	n/a
4	ARID3A	chr1:47081854-47082029	K562	blood:	n/a	n/a
5	ARID3A	chr1:47069629-47069860	K562	blood:	n/a	n/a
6	ARID3A	chr1:47070186-47070259	K562	blood:	n/a	n/a
7	ARID3A	chr1:47083799-47084297	HepG2	liver:	n/a	n/a
8	ATF1	chr1:47060945-47061249	K562	blood:	n/a	n/a
9	ATF1	chr1:47047399-47047856	K562	blood:	n/a	n/a
10	ATF1	chr1:47065356-47065411	K562	blood:	n/a	n/a
11	ATF1	chr1:47048676-47048980	K562	blood:	n/a	n/a
12	ATF1	chr1:47046294-47046511	K562	blood:	n/a	n/a
13	ATF3	chr1:47082190-47082462	K562	blood:	n/a	n/a
14	BACH1	chr1:47082703-47082950	K562	blood:	n/a	n/a
15	BACH1	chr1:47069664-47069834	K562	blood:	n/a	n/a
16	BACH1	chr1:47069595-47070012	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr1:47081911-47082740	H1-hESC	embryonic stem cell:	n/a	n/a
18	BACH1	chr1:47077460-47077619	H1-hESC	embryonic stem cell:	n/a	n/a
19	BACH1	chr1:47081522-47081670	H1-hESC	embryonic stem cell:	n/a	n/a
20	BACH1	chr1:47060942-47060990	K562	blood:	n/a	n/a
21	BCL3	chr1:47069608-47070248	GM12878	blood:	n/a	chr1:47069977-47069986
22	BCL3	chr1:47082395-47083126	A549	lung:	n/a	n/a
23	BCLAF1	chr1:47082163-47082843	GM12878	blood:	n/a	n/a
24	BHLHE40	chr1:47060991-47061154	K562	blood:	n/a	n/a
25	BHLHE40	chr1:47071985-47071986	HepG2	liver:	n/a	n/a
26	BHLHE40	chr1:47048683-47049007	K562	blood:	n/a	n/a
27	BHLHE40	chr1:47081937-47082856	GM12878	blood:	n/a	n/a
28	BHLHE40	chr1:47069163-47070325	GM12878	blood:	n/a	chr1:47069520-47069533 chr1:47069516-47069537
29	BHLHE40	chr1:47047554-47047863	K562	blood:	n/a	n/a
30	BHLHE40	chr1:47079257-47079945	GM12878	blood:	n/a	n/a
31	BHLHE40	chr1:47081880-47083091	K562	blood:	n/a	n/a
32	BHLHE40	chr1:47069411-47070237	K562	blood:	n/a	chr1:47069520-47069533 chr1:47069516-47069537
33	BRCA1	chr1:47069563-47070617	Hela-S3	cervix:	n/a	n/a
34	BRCA1	chr1:47069876-47069925	HepG2	liver:	n/a	n/a
35	BRCA1	chr1:47088192-47088410	Hela-S3	cervix:	n/a	n/a
36	BRCA1	chr1:47082270-47082469	GM12878	blood:	n/a	n/a
37	BRCA1	chr1:47069611-47069823	H1-hESC	embryonic stem cell:	n/a	n/a
38	BRCA1	chr1:47069323-47069399	GM12878	blood:	n/a	n/a
39	BRCA1	chr1:47069667-47069867	GM12878	blood:	n/a	n/a
40	CBX3	chr1:47081882-47082932	K562	blood:	n/a	n/a
41	CBX3	chr1:47069443-47070405	K562	blood:	n/a	n/a
42	CCNT2	chr1:47048728-47048910	K562	blood:	n/a	chr1:47048760-47048780
43	CCNT2	chr1:47082223-47082697	K562	blood:	n/a	n/a
44	CCNT2	chr1:47069546-47070172	K562	blood:	n/a	chr1:47069808-47069817 chr1:47069655-47069664
45	CCNT2	chr1:47089446-47089747	K562	blood:	n/a	n/a
46	CEBPB	chr1:47069525-47070295	GM12878	blood:	n/a	n/a
47	CEBPB	chr1:47088083-47088454	Hela-S3	cervix:	n/a	n/a
48	CEBPB	chr1:47052798-47052838	K562	blood:	n/a	chr1:47052824-47052835 chr1:47052823-47052834 chr1:47052823-47052836
49	CEBPB	chr1:47047584-47047858	K562	blood:	n/a	chr1:47047734-47047745
50	CEBPB	chr1:47069709-47070442	Hela-S3	cervix:	n/a	n/a

(count:2201 , 50 per page) page: 1 2 3 4 5 6 7 ... 45

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:47078649-47078699	PFSK-1	brain:	n/a
2	chr1:47082767-47082817	SK-N-SH	brain:	n/a
3	chr1:47070765-47070815	GM06990	blood:	n/a
4	chr1:47068636-47068686	HMEC	breast:	n/a
5	chr1:47070765-47070815	HAEpiC	amniotic membrane:	n/a
6	chr1:47078649-47078699	PFSK-1	brain:	n/a
7	chr1:47082767-47082817	SK-N-SH	brain:	n/a
8	chr1:47070765-47070815	GM06990	blood:	n/a
9	chr1:47068636-47068686	HMEC	breast:	n/a
10	chr1:47070765-47070815	HAEpiC	amniotic membrane:	n/a
11	chr1:47081524-47081574	HRE	kidney:	n/a
12	chr1:47070178-47070228	BJ	skin:	n/a
13	chr1:47082767-47082817	SKMC	muscle:	n/a
14	chr1:47082129-47082179	AG04449	skin:	fetal
15	chr1:47082211-47082261	MCF10A-Er-Src	breast:	n/a
16	chr1:47082037-47082087	ProgFib	skin:	n/a
17	chr1:47060645-47060695	Hela-S3	cervix:	n/a
18	chr1:47068636-47068686	LNCaP	prostate:	n/a
19	chr1:47082869-47082919	ECC-1	luminal epithelium:	n/a
20	chr1:47060645-47060695	PANC-1	pancreas:	n/a
21	chr1:47077680-47077730	BE2_C	brain:	n/a
22	chr1:47060645-47060695	HCPEpiC	choroid plexus:	n/a
23	chr1:47082211-47082261	HL-60	blood:	n/a
24	chr1:47066498-47066548	A549	lung:	n/a
25	chr1:47070058-47070108	ProgFib	skin:	n/a
26	chr1:47082851-47082901	HPAEpiC	pulmonary alveolar:	n/a
27	chr1:47078752-47078802	T-47D	breast:	n/a
28	chr1:47070807-47070857	HAEpiC	amniotic membrane:	n/a
29	chr1:47070176-47070226	HCM	heart:	n/a
30	chr1:47082129-47082179	CMK	blood:	n/a
31	chr1:47082211-47082261	HCM	heart:	n/a
32	chr1:47086491-47086541	ProgFib	skin:	n/a
33	chr1:47064750-47064800	GM12892	blood:	n/a
34	chr1:47082039-47082089	Jurkat	blood:	n/a
35	chr1:47078581-47078631	HCPEpiC	choroid plexus:	n/a
36	chr1:47082869-47082919	HCT-116	colon:	n/a
37	chr1:47079672-47079722	MCF-7	breast:	n/a
38	chr1:47068636-47068686	AG04449	skin:	fetal
39	chr1:47070052-47070102	HMEC	breast:	n/a
40	chr1:47078581-47078631	NT2-D1	testis:	n/a
41	chr1:47078966-47079016	GM12878	blood:	n/a
42	chr1:47082037-47082087	SK-N-SH	brain:	n/a
43	chr1:47060074-47060124	SK-N-MC	brain:	n/a
44	chr1:47081524-47081574	HRCEpiC	kidney:	n/a
45	chr1:47078649-47078699	HRCEpiC	kidney:	n/a
46	chr1:47082372-47082422	K562	blood:	n/a
47	chr1:47079672-47079722	RPTEC	kidney:	n/a
48	chr1:47069792-47069842	HCPEpiC	choroid plexus:	n/a
49	chr1:47077680-47077730	H1-hESC	embryonic stem cell:	embryo
50	chr1:47068636-47068686	GM12892	blood:	n/a

(count:74 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr1:47028417..47031367-chr1:47051984..47053721,2	K562	blood:
2	chr1:46912648..46913211-chr1:47041639..47042336,2	K562	blood:
3	chr1:47058514..47060124-chr1:47061743..47063610,2	MCF-7	breast:
4	chr1:47027064..47029429-chr1:47037828..47041063,3	K562	blood:
5	chr1:47086033..47090385-chr1:47091411..47095597,5	K562	blood:
6	chr1:47091302..47093763-chr1:47181587..47183697,2	K562	blood:
7	chr1:47073700..47076420-chr1:47091166..47093080,2	K562	blood:
8	chr1:47033343..47035201-chr1:47067108..47069992,2	K562	blood:
9	chr1:47081490..47084087-chr1:47086263..47088090,2	MCF-7	breast:
10	chr1:47076372..47077998-chr1:47081532..47083963,2	MCF-7	breast:
11	chr1:47069986..47078443-chr1:47078833..47084050,15	K562	blood:
12	chr1:47066512..47069474-chr1:47070954..47073416,4	K562	blood:
13	chr1:47062611..47065175-chr1:47080228..47083086,2	MCF-7	breast:
14	chr1:47073700..47076420-chr1:47091166..47093080,2	K562	blood:
15	chr1:47068429..47072503-chr1:47081068..47085092,4	MCF-7	breast:
16	chr1:47088932..47089596-chr1:47190617..47191353,2	MCF-7	breast:
17	chr1:47041717..47044206-chr1:47067000..47069818,2	K562	blood:
18	chr1:47038329..47041159-chr1:47076859..47079950,3	K562	blood:
19	chr1:47061375..47064454-chr1:47072882..47074737,3	K562	blood:
20	chr1:47049449..47051396-chr1:47063094..47066029,3	K562	blood:
21	chr1:47041661..47043778-chr1:47070091..47072496,2	K562	blood:
22	chr1:47052104..47053858-chr1:47055220..47057402,2	K562	blood:
23	chr1:47090932..47093400-chr1:47190525..47192623,2	MCF-7	breast:
24	chr1:47048260..47050517-chr1:47077583..47079223,2	K562	blood:
25	chr1:47054632..47056967-chr1:47067428..47069828,2	K562	blood:
26	chr1:47086033..47090385-chr1:47091411..47095597,5	K562	blood:
27	chr1:47050140..47053045-chr1:47054326..47056761,2	MCF-7	breast:
28	chr1:47077660..47081751-chr1:47132686..47135354,3	MCF-7	breast:
29	chr1:47048260..47050517-chr1:47077583..47079223,2	K562	blood:
30	chr1:47087818..47089652-chr1:47106481..47108594,2	MCF-7	breast:
31	chr1:47053959..47056132-chr1:47066697..47069062,3	K562	blood:
32	chr1:47080354..47082092-chr1:47110886..47112430,2	MCF-7	breast:
33	chr1:47078421..47080865-chr1:47080975..47083544,2	MCF-7	breast:
34	chr1:47076423..47078358-chr1:47078950..47080736,2	K562	blood:
35	chr1:47054104..47055847-chr1:47061988..47063605,2	K562	blood:
36	chr1:47069954..47072526-chr1:47696601..47699407,3	K562	blood:
37	chr1:47078421..47080865-chr1:47080975..47083544,2	MCF-7	breast:
38	chr1:47038566..47040285-chr1:47040736..47042855,2	K562	blood:
39	chr1:47041717..47044206-chr1:47067000..47069818,2	K562	blood:
40	chr1:47053775..47056193-chr1:47067460..47069823,2	MCF-7	breast:
41	chr1:47041661..47043778-chr1:47070091..47072496,2	K562	blood:
42	chr1:47040255..47042564-chr1:47053834..47056327,2	K562	blood:
43	chr1:47036966..47039803-chr1:47043494..47046451,2	K562	blood:
44	chr1:47046807..47049306-chr1:47050257..47052291,2	K562	blood:
45	chr1:47052682..47056987-chr1:47061043..47065460,4	K562	blood:
46	chr1:47061375..47064454-chr1:47072882..47074737,3	K562	blood:
47	chr1:47069390..47072755-chr1:47079314..47082367,4	MCF-7	breast:
48	chr1:47054104..47055847-chr1:47061988..47063605,2	K562	blood:
49	chr1:47087714..47088829-chr1:47190613..47191839,11	K562	blood:
50	chr1:47080724..47082396-chr1:47183672..47185631,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ATPAF1-AS1-3	chr1:47070418-47071240	NONHSAT003028
2	lnc-KNCN-3	chr1:47050176-47050475	NONHSAT003025
3	lnc-KNCN-3	chr1:47051546-47051941	NONHSAT003025

No data

Variant related genes	Relation type
MKNK1	TF binding region
MOB3C	TF binding region
MKNK1	CpG island
MOB3C	CpG island
ENSG00000186118	chromatin interactions
ENSG00000162367	chromatin interactions
ENSG00000142961	chromatin interactions
ENSG00000159658	chromatin interactions
ENSG00000123472	chromatin interactions
ENSG00000079277	chromatin interactions

Extended variants
information (count: 1989 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:1989 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs190929513	chr1:47040685-47040686	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs562451819	chr1:47040705-47040706	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs377573316	chr1:47040730-47040731	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs368973065	chr1:47040742-47040743	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs41305866	chr1:47040766-47040767	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs541604551	chr1:47040789-47040790	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs557520189	chr1:47040833-47040834	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs557868248	chr1:47040840-47040841	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs142321416	chr1:47040842-47040843	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs574166621	chr1:47040861-47040862	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs371515081	chr1:47040868-47040869	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs564279803	chr1:47040883-47040884	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs531741629	chr1:47040920-47040921	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs145940320	chr1:47040981-47040982	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs568764504	chr1:47041027-47041028	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs114887226	chr1:47041028-47041029	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs559439908	chr1:47041061-47041062	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs547991940	chr1:47041111-47041112	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs113365340	chr1:47041113-47041114	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs566277530	chr1:47041126-47041127	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs76927336	chr1:47041175-47041176	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs182435244	chr1:47041205-47041206	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs186184845	chr1:47041223-47041224	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs141679221	chr1:47041224-47041225	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs555770489	chr1:47041242-47041243	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs574376010	chr1:47041259-47041260	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs370839887	chr1:47041282-47041283	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs534080411	chr1:47041283-47041284	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs112399841	chr1:47041310-47041311	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs76688472	chr1:47041311-47041312	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs560146601	chr1:47041365-47041366	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs572211342	chr1:47041393-47041394	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs545939386	chr1:47041397-47041398	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs544939844	chr1:47041425-47041426	Weak transcription Enhancers Strong transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs564597333	chr1:47041520-47041521	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs190901004	chr1:47041522-47041523	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs376198560	chr1:47041583-47041584	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs530644268	chr1:47041588-47041589	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs375700776	chr1:47041592-47041593	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs113754619	chr1:47041604-47041605	Enhancers Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs56681125	chr1:47041606-47041607	Enhancers Strong transcription Weak transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs562095542	chr1:47041641-47041642	Enhancers Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs529574878	chr1:47041673-47041674	Enhancers Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs548131155	chr1:47041676-47041677	Enhancers Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs566093942	chr1:47041768-47041769	Enhancers Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs533580513	chr1:47041769-47041770	Enhancers Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs368360599	chr1:47041770-47041771	Enhancers Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs570507202	chr1:47041779-47041780	Enhancers Strong transcription Weak transcription Genic enhancers	CpG island	1 gene(s)	Overlapped CNVs	n/a
49	rs187325961	chr1:47041780-47041781	Enhancers Strong transcription Weak transcription Genic enhancers	CpG island	1 gene(s)	Overlapped CNVs	n/a
50	rs555705459	chr1:47041903-47041904	Enhancers Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:92)

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
Breast cancer	22522925	CNVD
Cancer	17440070	CNVD
Breast cancer	21990379	CNVD

Chromatin state (count:3205 , 50 per page) page: 1 2 3 4 5 6 7 ... 65

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:47015800-47041200	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr1:47015800-47043400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
3	chr1:47019800-47043600	Weak transcription	Dnd41	blood
4	chr1:47020800-47047400	Weak transcription	Brain Germinal Matrix	brain
5	chr1:47021000-47057000	Weak transcription	Fetal Brain Male	brain
6	chr1:47021200-47045000	Weak transcription	K562	blood
7	chr1:47021800-47054600	Weak transcription	A549	lung
8	chr1:47022200-47043400	Strong transcription	Primary neutrophils fromperipheralblood	blood
9	chr1:47022400-47053600	Strong transcription	Thymus	Thymus
10	chr1:47022600-47051400	Strong transcription	Skeletal Muscle Female	skeletal muscle
11	chr1:47022600-47051600	Strong transcription	Liver	Liver
12	chr1:47023000-47044200	Strong transcription	Monocytes-CD14+_RO01746	blood
13	chr1:47023000-47047400	Strong transcription	Primary T cells from cord blood	blood
14	chr1:47023200-47044400	Strong transcription	Primary monocytes fromperipheralblood	blood
15	chr1:47023200-47046600	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
16	chr1:47023200-47047200	Strong transcription	Fetal Thymus	thymus
17	chr1:47023200-47051200	Strong transcription	Fetal Muscle Leg	muscle
18	chr1:47023200-47060000	Strong transcription	Sigmoid Colon	Sigmoid Colon
19	chr1:47023400-47044600	Weak transcription	Muscle Satellite Cultured Cells	--
20	chr1:47023800-47045200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
21	chr1:47023800-47053200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
22	chr1:47024000-47054800	Weak transcription	HUVEC	blood vessel
23	chr1:47024600-47042400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
24	chr1:47025000-47041600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
25	chr1:47025600-47062400	Weak transcription	Fetal Heart	heart
26	chr1:47027000-47041000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
27	chr1:47027200-47047600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
28	chr1:47027600-47043400	Weak transcription	HepG2	liver
29	chr1:47028800-47041000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr1:47028800-47043600	Weak transcription	HMEC	breast
31	chr1:47028800-47044800	Weak transcription	Stomach Mucosa	stomach
32	chr1:47029000-47041800	Weak transcription	Placenta Amnion	Placenta Amnion
33	chr1:47029200-47042200	Weak transcription	NHLF	lung
34	chr1:47030800-47041000	Weak transcription	HUES6 Cell Line	embryonic stem cell
35	chr1:47030800-47046000	Weak transcription	Psoas Muscle	Psoas
36	chr1:47031000-47041800	Weak transcription	Brain Anterior Caudate	brain
37	chr1:47031200-47041000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
38	chr1:47031200-47045600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
39	chr1:47031400-47043400	Weak transcription	Osteobl	bone
40	chr1:47031600-47042000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
41	chr1:47031600-47042000	Weak transcription	Brain Cingulate Gyrus	brain
42	chr1:47032600-47046200	Strong transcription	Primary T cells fromperipheralblood	blood
43	chr1:47033000-47041200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr1:47033200-47042000	Weak transcription	Small Intestine	intestine
45	chr1:47033200-47043000	Weak transcription	Primary T helper cells PMA-I stimulated	--
46	chr1:47033400-47041000	Weak transcription	Fetal Brain Female	brain
47	chr1:47033600-47042400	Weak transcription	Colonic Mucosa	Colon
48	chr1:47034200-47042000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
49	chr1:47034200-47044800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
50	chr1:47035200-47044800	Strong transcription	Placenta	Placenta

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