Variant report

Variant	esv3529929
Chromosome Location	chr5:16748426-16856563
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1223)
CpG islands
(count:1100)
Chromatin interactive
region (count:54)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:1223 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:16776660-16777049	HepG2	liver:	n/a	n/a
2	ARID3A	chr5:16758093-16758785	HepG2	liver:	n/a	n/a
3	ARID3A	chr5:16809583-16809928	HepG2	liver:	n/a	n/a
4	ARID3A	chr5:16813151-16813325	HepG2	liver:	n/a	n/a
5	ARID3A	chr5:16774966-16775398	HepG2	liver:	n/a	chr5:16774972-16774988
6	ATF1	chr5:16784686-16784711	K562	blood:	n/a	n/a
7	ATF1	chr5:16778299-16778593	K562	blood:	n/a	n/a
8	ATF2	chr5:16785107-16785716	GM12878	blood:	n/a	n/a
9	ATF2	chr5:16784902-16785760	GM12878	blood:	n/a	n/a
10	ATF3	chr5:16778373-16778520	K562	blood:	n/a	n/a
11	ATF3	chr5:16778268-16778494	K562	blood:	n/a	n/a
12	BATF	chr5:16807279-16807538	GM12878	blood:	n/a	n/a
13	BATF	chr5:16785215-16785610	GM12878	blood:	n/a	n/a
14	BATF	chr5:16784669-16785693	GM12878	blood:	n/a	chr5:16784922-16784932 chr5:16784998-16785007
15	BCL11A	chr5:16785257-16785664	GM12878	blood:	n/a	chr5:16785445-16785454 chr5:16785326-16785335
16	BCL3	chr5:16785218-16785578	GM12878	blood:	n/a	chr5:16785445-16785454 chr5:16785235-16785244 chr5:16785326-16785335 chr5:16785228-16785241
17	BCLAF1	chr5:16785168-16785529	GM12878	blood:	n/a	chr5:16785445-16785454 chr5:16785235-16785244 chr5:16785326-16785335 chr5:16785228-16785241
18	BCLAF1	chr5:16785109-16785690	GM12878	blood:	n/a	chr5:16785445-16785454 chr5:16785235-16785244 chr5:16785326-16785335 chr5:16785228-16785241
19	BHLHE40	chr5:16778290-16778596	K562	blood:	n/a	n/a
20	BHLHE40	chr5:16783970-16784312	HepG2	liver:	n/a	n/a
21	BHLHE40	chr5:16791178-16791481	GM12878	blood:	n/a	n/a
22	BHLHE40	chr5:16785267-16785614	GM12878	blood:	n/a	n/a
23	BHLHE40	chr5:16749049-16749307	K562	blood:	n/a	chr5:16749138-16749151 chr5:16749134-16749155 chr5:16749140-16749149 chr5:16749141-16749150 chr5:16749139-16749148 chr5:16749140-16749149
24	BHLHE40	chr5:16823357-16823375	K562	blood:	n/a	n/a
25	BRCA1	chr5:16815522-16815992	Hela-S3	cervix:	n/a	n/a
26	BRCA1	chr5:16790290-16790376	HepG2	liver:	n/a	n/a
27	BRCA1	chr5:16776734-16777083	H1-hESC	embryonic stem cell:	n/a	n/a
28	BRCA1	chr5:16842553-16842554	GM12878	blood:	n/a	n/a
29	BRCA1	chr5:16776898-16777003	HepG2	liver:	n/a	n/a
30	CEBPB	chr5:16757676-16758807	HepG2	liver:	n/a	n/a
31	CEBPB	chr5:16774938-16775316	HepG2	liver:	n/a	n/a
32	CEBPB	chr5:16803066-16803202	H1-hESC	embryonic stem cell:	n/a	chr5:16803164-16803175
33	CEBPB	chr5:16803003-16803277	IMR90	lung:	n/a	chr5:16803164-16803175
34	CEBPB	chr5:16815635-16815804	K562	blood:	n/a	chr5:16815672-16815683
35	CEBPB	chr5:16840647-16840938	A549	lung:	n/a	chr5:16840818-16840827 chr5:16840816-16840829 chr5:16840816-16840829 chr5:16840816-16840827 chr5:16840817-16840828 chr5:16840816-16840829
36	CEBPB	chr5:16840668-16840956	IMR90	lung:	n/a	chr5:16840818-16840827 chr5:16840816-16840829 chr5:16840816-16840829 chr5:16840816-16840827 chr5:16840817-16840828 chr5:16840816-16840829
37	CEBPB	chr5:16815502-16815865	A549	lung:	n/a	chr5:16815672-16815683
38	CEBPB	chr5:16815497-16815872	IMR90	lung:	n/a	chr5:16815672-16815683
39	CEBPB	chr5:16833893-16834206	Hela-S3	cervix:	n/a	n/a
40	CEBPB	chr5:16819597-16820065	IMR90	lung:	n/a	n/a
41	CEBPB	chr5:16815420-16816009	Hela-S3	cervix:	n/a	chr5:16815672-16815683
42	CEBPB	chr5:16762502-16762750	HepG2	liver:	n/a	n/a
43	CEBPB	chr5:16803018-16803218	HepG2	liver:	n/a	chr5:16803164-16803175
44	CEBPB	chr5:16815480-16815952	MCF-7	breast:	n/a	chr5:16815672-16815683
45	CEBPB	chr5:16778282-16778453	K562	blood:	n/a	n/a
46	CEBPB	chr5:16854617-16855206	IMR90	lung:	n/a	chr5:16854744-16854755
47	CEBPB	chr5:16758138-16758407	HepG2	liver:	n/a	n/a
48	CEBPB	chr5:16835079-16835343	A549	lung:	n/a	chr5:16835236-16835247
49	CEBPB	chr5:16815403-16816004	A549	lung:	n/a	chr5:16815672-16815683
50	CEBPB	chr5:16840701-16840873	Hela-S3	cervix:	n/a	chr5:16840818-16840827 chr5:16840816-16840829 chr5:16840816-16840829 chr5:16840816-16840827 chr5:16840817-16840828 chr5:16840816-16840829

(count:1100 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:16820044-16820094	HEK293	kidney:	embryo
2	chr5:16784821-16784871	SK-N-MC	brain:	n/a
3	chr5:16820044-16820094	HEK293	kidney:	embryo
4	chr5:16784821-16784871	SK-N-MC	brain:	n/a
5	chr5:16794840-16794890	MCF10A-Er-Src	breast:	n/a
6	chr5:16812392-16812442	U87	brain:	n/a
7	chr5:16828148-16828198	LNCaP	prostate:	n/a
8	chr5:16784821-16784871	AG04449	skin:	fetal
9	chr5:16792048-16792098	Caco-2	colon:	n/a
10	chr5:16843340-16843390	Jurkat	blood:	n/a
11	chr5:16784951-16785001	K562	blood:	n/a
12	chr5:16784775-16784825	ECC-1	luminal epithelium:	n/a
13	chr5:16785051-16785101	MCF10A-Er-Src	breast:	n/a
14	chr5:16754384-16754434	HEK293	kidney:	embryo
15	chr5:16783782-16783832	HIPEpiC	eye:	n/a
16	chr5:16828148-16828198	ProgFib	skin:	n/a
17	chr5:16812392-16812442	K562	blood:	n/a
18	chr5:16843340-16843390	BJ	skin:	n/a
19	chr5:16784775-16784825	K562	blood:	n/a
20	chr5:16777377-16777427	HMEC	breast:	n/a
21	chr5:16777377-16777427	NH-A	brain:	n/a
22	chr5:16812392-16812442	H1-hESC	embryonic stem cell:	embryo
23	chr5:16784821-16784871	SKMC	muscle:	n/a
24	chr5:16784821-16784871	PANC-1	pancreas:	n/a
25	chr5:16828148-16828198	NT2-D1	testis:	n/a
26	chr5:16843340-16843390	GM12878	blood:	n/a
27	chr5:16777377-16777427	HRCEpiC	kidney:	n/a
28	chr5:16777377-16777427	H1-hESC	embryonic stem cell:	embryo
29	chr5:16794840-16794890	MCF-7	breast:	n/a
30	chr5:16777377-16777427	HRE	kidney:	n/a
31	chr5:16785051-16785101	ECC-1	luminal epithelium:	n/a
32	chr5:16794882-16794932	HCT-116	colon:	n/a
33	chr5:16785399-16785449	SAEC	small airway:	n/a
34	chr5:16843340-16843390	SAEC	small airway:	n/a
35	chr5:16820044-16820094	AG09319	gingival:	n/a
36	chr5:16784821-16784871	U87	brain:	n/a
37	chr5:16792048-16792098	HIPEpiC	eye:	n/a
38	chr5:16794882-16794932	SKMC	muscle:	n/a
39	chr5:16794797-16794847	HCPEpiC	choroid plexus:	n/a
40	chr5:16785051-16785101	Hela-S3	cervix:	n/a
41	chr5:16792048-16792098	T-47D	breast:	n/a
42	chr5:16783782-16783832	HepG2	liver:	n/a
43	chr5:16783782-16783832	U87	brain:	n/a
44	chr5:16794797-16794847	PFSK-1	brain:	n/a
45	chr5:16854566-16854616	GM12891	blood:	n/a
46	chr5:16785399-16785449	A549	lung:	n/a
47	chr5:16784821-16784871	SK-N-SH_RA	brain:	n/a
48	chr5:16784951-16785001	SK-N-MC	brain:	n/a
49	chr5:16784821-16784871	RPTEC	kidney:	n/a
50	chr5:16784821-16784871	K562	blood:	n/a

(count:54 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr5:16844716..16845739-chr5:17189554..17191043,3	MCF-7	breast:
2	chr5:16804606..16806636-chr5:17187193..17189574,2	MCF-7	breast:
3	chr5:16848554..16850179-chr5:16855617..16858396,2	K562	blood:
4	chr5:16740840..16741721-chr5:16776516..16777353,6	MCF-7	breast:
5	chr5:16784701..16787932-chr5:16789785..16793090,3	MCF-7	breast:
6	chr5:16845210..16846751-chr5:16934802..16937516,2	MCF-7	breast:
7	chr5:16790349..16791141-chr5:17188352..17189070,2	MCF-7	breast:
8	chr5:16740780..16741704-chr5:16776541..16777578,3	MCF-7	breast:
9	chr5:16769084..16770925-chr5:16772058..16775027,2	K562	blood:
10	chr5:16812869..16815029-chr5:16819964..16822225,2	MCF-7	breast:
11	chr5:16803642..16805897-chr5:16806344..16809776,4	MCF-7	breast:
12	chr5:16812869..16815029-chr5:16819964..16822225,2	MCF-7	breast:
13	chr5:16791251..16792040-chr5:17189230..17190196,3	K562	blood:
14	chr5:16850266..16851821-chr5:16858055..16860279,2	MCF-7	breast:
15	chr5:16848554..16850179-chr5:16855617..16858396,2	K562	blood:
16	chr5:16844722..16845699-chr5:17190257..17190921,4	MCF-7	breast:
17	chr5:16743803..16745620-chr5:16745640..16748516,2	K562	blood:
18	chr5:16803642..16805897-chr5:16806344..16809776,4	MCF-7	breast:
19	chr5:16844825..16845663-chr5:17132355..17133261,2	MCF-7	breast:
20	chr5:16791251..16791880-chr5:17203236..17203800,2	MCF-7	breast:
21	chr5:16791277..16791811-chr5:17190344..17190933,2	K562	blood:
22	chr5:16744168..16745132-chr5:16787048..16788082,5	MCF-7	breast:
23	chr5:16755698..16757914-chr5:16758112..16760013,3	MCF-7	breast:
24	chr5:16744561..16747041-chr5:16752220..16754067,2	K562	blood:
25	chr5:16852586..16854370-chr5:16854403..16855984,2	K562	blood:
26	chr5:16756542..16758777-chr5:16782954..16785752,2	K562	blood:
27	chr5:16690107..16691016-chr5:16776506..16777632,8	MCF-7	breast:
28	chr14:77519468..77520138-chr5:16844783..16845778,2	MCF-7	breast:
29	chr5:16803694..16804550-chr5:17190688..17191667,2	MCF-7	breast:
30	chr5:16744168..16745132-chr5:16787048..16788082,8	MCF-7	breast:
31	chr5:16844822..16845733-chr5:17189257..17190121,5	MCF-7	breast:
32	chr5:16855463..16857293-chr5:16859556..16861090,2	MCF-7	breast:
33	chr5:16790925..16791832-chr5:17188820..17190182,5	MCF-7	breast:
34	chr5:16679668..16680619-chr5:16776494..16777357,4	MCF-7	breast:
35	chr5:16854713..16857141-chr5:16861779..16864325,2	MCF-7	breast:
36	chr5:16784701..16787932-chr5:16789785..16793090,3	MCF-7	breast:
37	chr5:16791046..16792329-chr5:17190230..17191251,5	MCF-7	breast:
38	chr5:16827134..16829688-chr5:16861859..16863470,2	MCF-7	breast:
39	chr5:16690385..16690941-chr5:16790933..16791791,2	MCF-7	breast:
40	chr5:16844783..16845610-chr5:16933834..16934784,3	MCF-7	breast:
41	chr5:16844775..16845487-chr5:17132389..17133714,4	MCF-7	breast:
42	chr5:16788946..16790699-chr5:16935201..16936930,2	MCF-7	breast:
43	chr5:16782557..16785455-chr5:16934978..16937136,2	MCF-7	breast:
44	chr5:16690101..16691036-chr5:16776467..16777868,10	MCF-7	breast:
45	chr5:16849069..16851514-chr5:16934765..16937282,2	MCF-7	breast:
46	chr5:16791035..16791887-chr5:17189190..17190176,6	MCF-7	breast:
47	chr5:16790795..16791796-chr5:17132341..17133331,6	MCF-7	breast:
48	chr5:16763622..16766188-chr5:16934397..16936475,2	MCF-7	breast:
49	chr5:16790873..16791809-chr5:17203163..17204098,3	K562	blood:
50	chr5:16805947..16808433-chr5:16911651..16914280,2	MCF-7	breast:

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	MYO10	hsa-miR-26a-5p	chr5:16814636-16814657

Variant related genes	Relation type
MYO10	TF binding region
RNA5SP179	TF binding region
MYO10	CpG island
RNA5SP179	CpG island
ENSG00000253093	chromatin interactions
ENSG00000145555	chromatin interactions

Extended variants
information (count: 4802 )
Associated
traits (count: 93 )

Variant overlapped rSNPs/rCNVs (count:4802 , 50 per page) page: 1 2 3 4 5 6 7 ... 97

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs564605760	chr5:16748454-16748455	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs374250456	chr5:16748502-16748503	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs576365345	chr5:16748547-16748548	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs543500606	chr5:16748556-16748557	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs562009316	chr5:16748566-16748567	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs11950985	chr5:16748583-16748584	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs367850825	chr5:16748596-16748597	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs540329632	chr5:16748599-16748600	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs574623698	chr5:16748600-16748601	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs559090730	chr5:16748602-16748603	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs377374094	chr5:16748603-16748604	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs532977793	chr5:16748606-16748607	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs10037703	chr5:16748607-16748608	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs550673480	chr5:16748608-16748609	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs551047739	chr5:16748630-16748631	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs183891902	chr5:16748650-16748651	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs537047910	chr5:16748659-16748660	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs187883097	chr5:16748664-16748665	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs143045493	chr5:16748714-16748715	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs34860839	chr5:16748719-16748720	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs376211778	chr5:16748721-16748722	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs368473711	chr5:16748722-16748723	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs386685856	chr5:16748726-16748727	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs10072360	chr5:16748730-16748731	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs34338717	chr5:16748731-16748732	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs11951017	chr5:16748734-16748735	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs386685857	chr5:16748738-16748739	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs146076291	chr5:16748746-16748747	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs377750666	chr5:16748757-16748758	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs548745006	chr5:16748783-16748784	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs138816209	chr5:16748869-16748870	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs115587172	chr5:16748970-16748971	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs35953104	chr5:16749025-16749026	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs398083947	chr5:16749029-16749030	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs397882671	chr5:16749030-16749031	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs368176566	chr5:16749052-16749053	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs191585263	chr5:16749062-16749063	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs572661134	chr5:16749097-16749098	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs142621174	chr5:16749100-16749101	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs558227257	chr5:16749101-16749102	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs370753677	chr5:16749141-16749142	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs576498987	chr5:16749168-16749169	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs543904389	chr5:16749169-16749170	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs561884361	chr5:16749215-16749216	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs573997249	chr5:16749246-16749247	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs558644155	chr5:16749247-16749248	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs371950398	chr5:16749279-16749280	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs540895542	chr5:16749280-16749281	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs182237038	chr5:16749287-16749288	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs77187024	chr5:16749293-16749294	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:93)

Disease	PMID	Source
Lung cancer	19547694	CNVD
Cri-du chat syndrome	22283845	CNVD
Disorders of sex development	21048976	CNVD
Non-small cell lung cancer	20864512	CNVD
Cancer	21183584	CNVD
Cervical squamous cell carcinoma	21590768	CNVD
Honadal dysgenesis	21048976	CNVD
Cancer	16751803	CNVD
Breast cancer	17133270	CNVD
Hepatocellular carcinoma	22174799	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Salivary gland tumor	18059337	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Kartagener syndrome	16639409	CNVD
Medulloblastoma	21979893	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	16783165	CNVD
Thyroid cancer	19087340	CNVD
Liposarcoma	21253554	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Cervical Cancer	21857958	CNVD
Cervical cancer	21062161	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Oral cancer	21386901	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Ewing''s sarcoma	17952124	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Cervical cancer	18559093	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Metanephric adenoma	20802469	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Colorectal cancer	21645411	CNVD
Gastric cancer	22152101	CNVD
Oesophago-gastric ulcer	22152101	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Cancer	20164919	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Multiple myeloma	17550852	CNVD
prenatal diagnosis	22389664	CNVD
Bladder cancer	21909424	CNVD
DNA damage stimulus	22844521	CNVD
DNA repair	22844521	CNVD
Breast cancer	21785460	CNVD
Spinal muscular atrophy	22422766	CNVD
Spinal muscular atrophy	22558076	CNVD
Spinal muscular atrophy	21320981	CNVD
Spinal muscular atrophy	21762474	CNVD
Breast cancer	21858162	CNVD
Prostate cancer	18632612	CNVD
Esophageal adenocarcinoma	19417022	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	16608533	CNVD
Anaplastic large cell lymphoma	18179710	CNVD
Autism	22495311	CNVD
Melanoma	18172304	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Intellectual disability	22102821	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Williams Syndrome	20824207	CNVD
Breast cancer	21364760	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Acute lymphoblastic leukemia	17640729	CNVD
Myoepithelioma	18604193	CNVD
Lung cancer	16740712	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Melanoma	22183965	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:2385 , 50 per page) page: 1 2 3 4 5 6 7 ... 48

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:16736400-16781400	Weak transcription	Esophagus	oesophagus
2	chr5:16736800-16756600	Weak transcription	Ovary	ovary
3	chr5:16736800-16758200	Weak transcription	Spleen	Spleen
4	chr5:16736800-16761200	Weak transcription	Hela-S3	cervix
5	chr5:16736800-16761800	Weak transcription	Colonic Mucosa	Colon
6	chr5:16736800-16762400	Weak transcription	Skeletal Muscle Female	skeletal muscle
7	chr5:16737000-16780400	Weak transcription	Pancreatic Islets	Pancreatic Islet
8	chr5:16738400-16748800	Weak transcription	Sigmoid Colon	Sigmoid Colon
9	chr5:16739200-16750600	Weak transcription	Muscle Satellite Cultured Cells	--
10	chr5:16739400-16758000	Weak transcription	Stomach Mucosa	stomach
11	chr5:16741000-16755800	Weak transcription	Placenta Amnion	Placenta Amnion
12	chr5:16741000-16758400	Weak transcription	Aorta	Aorta
13	chr5:16741200-16782000	Weak transcription	Rectal Smooth Muscle	rectum
14	chr5:16741400-16754600	Weak transcription	Fetal Kidney	kidney
15	chr5:16741800-16761400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
16	chr5:16742200-16751800	Weak transcription	H9 Cell Line	embryonic stem cell
17	chr5:16742200-16752000	Weak transcription	Stomach Smooth Muscle	stomach
18	chr5:16742200-16752600	Weak transcription	NHEK	skin
19	chr5:16742400-16757800	Weak transcription	Adipose Nuclei	Adipose
20	chr5:16742400-16761800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
21	chr5:16742400-16773400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
22	chr5:16742600-16749000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
23	chr5:16742600-16749600	Weak transcription	NHLF	lung
24	chr5:16742600-16750000	Weak transcription	Brain Germinal Matrix	brain
25	chr5:16742800-16749600	Weak transcription	Fetal Muscle Leg	muscle
26	chr5:16742800-16751200	Weak transcription	NHDF-Ad	bronchial
27	chr5:16742800-16754400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
28	chr5:16742800-16767800	Weak transcription	Fetal Brain Female	brain
29	chr5:16743400-16750600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
30	chr5:16743400-16753800	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr5:16743400-16760800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr5:16743600-16777600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
33	chr5:16743800-16749800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
34	chr5:16744000-16754200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr5:16744000-16754200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
36	chr5:16744600-16749200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
37	chr5:16744800-16749000	Weak transcription	Lung	lung
38	chr5:16744800-16749000	Weak transcription	Rectal Mucosa Donor 31	rectum
39	chr5:16744800-16749200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
40	chr5:16744800-16749800	Weak transcription	H1 Cell Line	embryonic stem cell
41	chr5:16744800-16750200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
42	chr5:16744800-16753800	Weak transcription	HSMM	muscle
43	chr5:16744800-16755600	Weak transcription	Fetal Lung	lung
44	chr5:16744800-16758400	Weak transcription	Gastric	stomach
45	chr5:16744800-16776800	Weak transcription	Left Ventricle	heart
46	chr5:16745000-16751400	Weak transcription	HUES48 Cell Line	embryonic stem cell
47	chr5:16745200-16752000	Weak transcription	HUES64 Cell Line	embryonic stem cell
48	chr5:16745800-16758600	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
49	chr5:16746000-16778200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
50	chr5:16746200-16749800	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

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