Variant report

Variant	nsv869660
Chromosome Location	chr5:16651289-16766428
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1533)
CpG islands
(count:1953)
Chromatin interactive
region (count:70)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:2)

(count:1533 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:16690396-16690588	HepG2	liver:	n/a	n/a
2	ARID3A	chr5:16744451-16745115	HepG2	liver:	n/a	n/a
3	ARID3A	chr5:16758093-16758785	HepG2	liver:	n/a	n/a
4	ARID3A	chr5:16720946-16721021	HepG2	liver:	n/a	n/a
5	ARID3A	chr5:16721260-16722161	HepG2	liver:	n/a	n/a
6	ARID3A	chr5:16735812-16736834	HepG2	liver:	n/a	n/a
7	ATF1	chr5:16736365-16736678	K562	blood:	n/a	n/a
8	ATF1	chr5:16690389-16690589	K562	blood:	n/a	n/a
9	ATF1	chr5:16724177-16724408	K562	blood:	n/a	n/a
10	ATF2	chr5:16741921-16742549	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF2	chr5:16741571-16742550	H1-hESC	embryonic stem cell:	n/a	n/a
12	ATF2	chr5:16740175-16741547	H1-hESC	embryonic stem cell:	n/a	n/a
13	ATF3	chr5:16736376-16736655	HepG2	liver:	n/a	n/a
14	ATF3	chr5:16736361-16736650	K562	blood:	n/a	n/a
15	ATF3	chr5:16736340-16736720	H1-hESC	embryonic stem cell:	n/a	n/a
16	BACH1	chr5:16736158-16736481	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr5:16679398-16679599	H1-hESC	embryonic stem cell:	n/a	n/a
18	BACH1	chr5:16721328-16721329	H1-hESC	embryonic stem cell:	n/a	n/a
19	BCL11A	chr5:16741039-16741292	H1-hESC	embryonic stem cell:	n/a	n/a
20	BCL3	chr5:16660391-16660707	A549	lung:	n/a	n/a
21	BCL3	chr5:16661022-16661835	A549	lung:	n/a	chr5:16661707-16661714
22	BCL3	chr5:16661048-16661518	A549	lung:	n/a	n/a
23	BHLHE40	chr5:16667128-16667155	K562	blood:	n/a	n/a
24	BHLHE40	chr5:16673020-16673035	K562	blood:	n/a	n/a
25	BHLHE40	chr5:16736477-16736545	K562	blood:	n/a	n/a
26	BHLHE40	chr5:16673401-16673596	K562	blood:	n/a	chr5:16673443-16673452
27	BHLHE40	chr5:16736190-16736855	HepG2	liver:	n/a	n/a
28	BHLHE40	chr5:16731841-16732008	K562	blood:	n/a	chr5:16731943-16731952 chr5:16731937-16731958 chr5:16731943-16731952 chr5:16731942-16731951
29	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
30	BHLHE40	chr5:16721328-16721574	HepG2	liver:	n/a	n/a
31	BRCA1	chr5:16690664-16690715	HepG2	liver:	n/a	n/a
32	BRCA1	chr5:16740663-16741478	H1-hESC	embryonic stem cell:	n/a	chr5:16741308-16741315
33	BRCA1	chr5:16664706-16664714	HepG2	liver:	n/a	n/a
34	CEBPB	chr5:16743613-16744076	HepG2	liver:	n/a	chr5:16743974-16743985
35	CEBPB	chr5:16736230-16736871	ECC-1	luminal epithelium:	n/a	n/a
36	CEBPB	chr5:16736361-16736634	HepG2	liver:	n/a	n/a
37	CEBPB	chr5:16656687-16656939	Hela-S3	cervix:	n/a	chr5:16656796-16656807
38	CEBPB	chr5:16757675-16758743	HepG2	liver:	n/a	n/a
39	CEBPB	chr5:16736277-16736843	MCF-7	breast:	n/a	n/a
40	CEBPB	chr5:16669843-16670169	IMR90	lung:	n/a	n/a
41	CEBPB	chr5:16746448-16746652	HepG2	liver:	n/a	chr5:16746621-16746632
42	CEBPB	chr5:16685310-16685494	HepG2	liver:	n/a	chr5:16685375-16685386
43	CEBPB	chr5:16736198-16736903	HCT-116	colon:	n/a	n/a
44	CEBPB	chr5:16656663-16656955	HepG2	liver:	n/a	chr5:16656796-16656807
45	CEBPB	chr5:16736258-16736684	HepG2	liver:	n/a	n/a
46	CEBPB	chr5:16736351-16736687	K562	blood:	n/a	n/a
47	CEBPB	chr5:16736313-16736804	HepG2	liver:	n/a	n/a
48	CEBPB	chr5:16757676-16758807	HepG2	liver:	n/a	n/a
49	CEBPB	chr5:16758138-16758407	HepG2	liver:	n/a	n/a
50	CEBPB	chr5:16736311-16736727	Hela-S3	cervix:	n/a	n/a

(count:1953 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:16742020-16742070	AG09309	skin:	n/a
2	chr5:16742020-16742070	AG09309	skin:	n/a
3	chr5:16701581-16701631	NT2-D1	testis:	n/a
4	chr5:16736823-16736873	ovcar-3	ovarian:	n/a
5	chr5:16700411-16700461	NH-A	brain:	n/a
6	chr5:16742020-16742070	NB4	blood:	n/a
7	chr5:16737972-16738022	HEK293	kidney:	embryo
8	chr5:16670826-16670876	AG10803	skin:	n/a
9	chr5:16670826-16670876	SK-N-MC	brain:	n/a
10	chr5:16721797-16721847	ovcar-3	ovarian:	n/a
11	chr5:16737972-16738022	Jurkat	blood:	n/a
12	chr5:16670964-16671014	HepG2	liver:	n/a
13	chr5:16738125-16738175	HEK293	kidney:	embryo
14	chr5:16738049-16738099	ProgFib	skin:	n/a
15	chr5:16669915-16669965	PANC-1	pancreas:	n/a
16	chr5:16664426-16664476	SAEC	small airway:	n/a
17	chr5:16701575-16701625	RPTEC	kidney:	n/a
18	chr5:16754384-16754434	GM06990	blood:	n/a
19	chr5:16698129-16698179	AoSMC	blood vessel:	n/a
20	chr5:16713588-16713638	HRCEpiC	kidney:	n/a
21	chr5:16703715-16703765	AoSMC	blood vessel:	n/a
22	chr5:16738318-16738368	PrEC	prostate:	n/a
23	chr5:16742020-16742070	SAEC	small airway:	n/a
24	chr5:16728219-16728269	U87	brain:	n/a
25	chr5:16667384-16667434	LNCaP	prostate:	n/a
26	chr5:16754384-16754434	PrEC	prostate:	n/a
27	chr5:16754384-16754434	SKMC	muscle:	n/a
28	chr5:16700411-16700461	HRPEpiC	eye:	n/a
29	chr5:16742054-16742104	A549	lung:	n/a
30	chr5:16736823-16736873	AG10803	skin:	n/a
31	chr5:16667384-16667434	HCF	heart:	n/a
32	chr5:16738125-16738175	GM12891	blood:	n/a
33	chr5:16737972-16738022	SK-N-MC	brain:	n/a
34	chr5:16738125-16738175	RPTEC	kidney:	n/a
35	chr5:16664426-16664476	MCF-7	breast:	n/a
36	chr5:16738318-16738368	HRPEpiC	eye:	n/a
37	chr5:16738125-16738175	SK-N-SH	brain:	n/a
38	chr5:16669915-16669965	PrEC	prostate:	n/a
39	chr5:16701387-16701437	H1-hESC	embryonic stem cell:	embryo
40	chr5:16667384-16667434	NT2-D1	testis:	n/a
41	chr5:16669915-16669965	GM12892	blood:	n/a
42	chr5:16754384-16754434	T-47D	breast:	n/a
43	chr5:16664426-16664476	K562	blood:	n/a
44	chr5:16737972-16738022	NHDF-neo	bronchial:	n/a
45	chr5:16738049-16738099	ECC-1	luminal epithelium:	n/a
46	chr5:16671496-16671546	HCT-116	colon:	n/a
47	chr5:16742054-16742104	HCT-116	colon:	n/a
48	chr5:16743265-16743315	RPTEC	kidney:	n/a
49	chr5:16742179-16742229	ProgFib	skin:	n/a
50	chr5:16703715-16703765	HCM	heart:	n/a

(count:70 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr5:16744168..16745132-chr5:16787048..16788082,5	MCF-7	breast:
2	chr5:16743803..16745620-chr5:16745640..16748516,2	K562	blood:
3	chr5:16588242..16589515-chr5:16744207..16745107,7	MCF-7	breast:
4	chr5:16699313..16701301-chr5:16704583..16706193,2	K562	blood:
5	chr5:16690097..16690919-chr5:17190336..17190908,2	MCF-7	breast:
6	chr5:16680167..16682667-chr5:16701918..16704476,2	MCF-7	breast:
7	chr5:16723686..16725760-chr5:16727885..16730861,2	MCF-7	breast:
8	chr5:16552702..16553520-chr5:16666199..16667543,5	MCF-7	breast:
9	chr5:16491553..16492366-chr5:16666413..16667129,2	MCF-7	breast:
10	chr5:16755698..16757914-chr5:16758112..16760013,3	MCF-7	breast:
11	chr5:16744168..16745132-chr5:16787048..16788082,8	MCF-7	breast:
12	chr5:16679668..16680619-chr5:16776494..16777357,4	MCF-7	breast:
13	chr5:16588242..16589198-chr5:16744257..16744813,2	MCF-7	breast:
14	chr5:16723548..16725058-chr5:16725138..16727326,2	MCF-7	breast:
15	chr5:16489048..16489981-chr5:16666700..16667736,8	MCF-7	breast:
16	chr5:16489475..16489994-chr5:16681988..16682546,2	MCF-7	breast:
17	chr5:16596048..16598772-chr5:16707141..16709830,2	K562	blood:
18	chr5:16693261..16695591-chr5:16699683..16702377,2	MCF-7	breast:
19	chr5:16690107..16691016-chr5:16776506..16777632,8	MCF-7	breast:
20	chr5:16743803..16745620-chr5:16745640..16748516,2	K562	blood:
21	chr5:16626745..16627365-chr5:16744383..16745128,3	MCF-7	breast:
22	chr5:16710425..16712025-chr5:16715112..16717325,2	MCF-7	breast:
23	chr5:16690385..16690941-chr5:16790933..16791791,2	MCF-7	breast:
24	chr5:16667013..16667892-chr5:16690340..16691325,2	MCF-7	breast:
25	chr5:16727860..16733317-chr5:16734761..16739949,6	MCF-7	breast:
26	chr5:16690101..16691036-chr5:16776467..16777868,10	MCF-7	breast:
27	chr5:16463003..16466363-chr5:16662397..16665383,3	MCF-7	breast:
28	chr5:16552594..16553429-chr5:16666387..16667201,2	MCF-7	breast:
29	chr5:16693261..16695591-chr5:16699683..16702377,2	MCF-7	breast:
30	chr5:16763622..16766188-chr5:16934397..16936475,2	MCF-7	breast:
31	chr5:16664373..16665926-chr5:16667550..16669160,2	K562	blood:
32	chr5:16723548..16725058-chr5:16725138..16727326,2	MCF-7	breast:
33	chr5:16728548..16730757-chr5:16733455..16736411,2	MCF-7	breast:
34	chr5:16626745..16627365-chr5:16744294..16745128,4	MCF-7	breast:
35	chr5:16729939..16731528-chr5:16732175..16733967,2	MCF-7	breast:
36	chr5:16729939..16731528-chr5:16732175..16733967,2	MCF-7	breast:
37	chr5:16492613..16493345-chr5:16666414..16667024,2	MCF-7	breast:
38	chr5:16728548..16730757-chr5:16733455..16736411,2	MCF-7	breast:
39	chr5:16670338..16672249-chr5:16672358..16674195,2	MCF-7	breast:
40	chr5:16699313..16701301-chr5:16704583..16706193,2	K562	blood:
41	chr5:16713673..16715499-chr5:16715772..16717770,2	K562	blood:
42	chr5:16236004..16236570-chr5:16690055..16690976,2	K562	blood:
43	chr5:16713673..16715499-chr5:16715772..16717770,2	K562	blood:
44	chr5:16664373..16665926-chr5:16667550..16669160,2	K562	blood:
45	chr5:16734341..16736922-chr5:16738909..16741583,2	MCF-7	breast:
46	chr5:16667013..16667892-chr5:16690340..16691325,2	MCF-7	breast:
47	chr5:16710355..16712259-chr5:16729265..16730891,2	MCF-7	breast:
48	chr1:9356327..9359278-chr5:16672338..16674681,2	MCF-7	breast:
49	chr5:16588416..16589500-chr5:16674631..16675555,5	MCF-7	breast:
50	chr5:16734341..16736922-chr5:16738909..16741583,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-BASP1-12	chr5:16661231-16661482	NONHSAT100613

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	MYO10	hsa-miR-155-5p	chr5:16666155-16666183
2	MYO10	hsa-miR-155-5p	chr5:16666161-16666154

Variant related genes	Relation type
MYO10	TF binding region
MYO10	CpG island
ENSG00000145555	chromatin interactions
ENSG00000154153	chromatin interactions
ENSG00000173545	chromatin interactions

Extended variants
information (count: 5248 )
Associated
traits (count: 94 )

Variant overlapped rSNPs/rCNVs (count:5248 , 50 per page) page: 1 2 3 4 5 6 7 ... 105

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs531900498	chr5:16651308-16651309	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs550401527	chr5:16651386-16651387	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs568567233	chr5:16651393-16651394	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs535997182	chr5:16651401-16651402	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs12109865	chr5:16651405-16651406	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs544904294	chr5:16651427-16651428	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs566095174	chr5:16651461-16651462	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs539470082	chr5:16651464-16651465	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs150884824	chr5:16651468-16651469	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs446224	chr5:16651469-16651470	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs377309	chr5:16651472-16651473	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs113454689	chr5:16651482-16651483	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs188737306	chr5:16651490-16651491	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs181175105	chr5:16651505-16651506	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs13188167	chr5:16651545-16651546	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs149598709	chr5:16651564-16651565	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs559062711	chr5:16651573-16651574	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs557117740	chr5:16651598-16651599	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs549504984	chr5:16651600-16651601	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs146058629	chr5:16651609-16651610	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs186255345	chr5:16651622-16651623	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs190362718	chr5:16651632-16651633	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs181689784	chr5:16651639-16651640	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs568707714	chr5:16651647-16651648	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs529387041	chr5:16651648-16651649	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs531837190	chr5:16651651-16651652	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs547843535	chr5:16651653-16651654	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs186438057	chr5:16651656-16651657	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs252370	chr5:16651658-16651659	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs571535859	chr5:16651665-16651666	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs539777638	chr5:16651670-16651671	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs430708	chr5:16651673-16651674	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs190717598	chr5:16651709-16651710	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs201636643	chr5:16651723-16651724	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs536988507	chr5:16651744-16651745	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs556882626	chr5:16651753-16651754	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs555126595	chr5:16651782-16651783	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs182238035	chr5:16651814-16651815	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs534525764	chr5:16651827-16651828	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs552993873	chr5:16651833-16651834	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs577667273	chr5:16651933-16651934	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs538938522	chr5:16651943-16651944	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs10064723	chr5:16651945-16651946	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs563180134	chr5:16651981-16651982	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs547328550	chr5:16652025-16652026	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs576796360	chr5:16652043-16652044	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs544157718	chr5:16652066-16652067	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs12655691	chr5:16652068-16652069	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs201099646	chr5:16652075-16652076	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs12659860	chr5:16652084-16652085	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:94)

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
Non-syndromic sensorineural hearing loss	22037309	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:3600 , 50 per page) page: 1 2 3 4 5 6 7 ... 72

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:16650000-16664600	Weak transcription	H1 Cell Line	embryonic stem cell
2	chr5:16652600-16663000	Weak transcription	Primary T cells from cord blood	blood
3	chr5:16653800-16663600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
4	chr5:16655000-16655200	Enhancers	Hela-S3	cervix
5	chr5:16655200-16655400	Weak transcription	Hela-S3	cervix
6	chr5:16655600-16655800	Enhancers	Esophagus	oesophagus
7	chr5:16655600-16655800	ZNF genes & repeats	Pancreas	Pancrea
8	chr5:16655600-16655800	Bivalent Enhancer	NHDF-Ad	bronchial
9	chr5:16655800-16664000	Weak transcription	Pancreas	Pancrea
10	chr5:16655800-16670600	Weak transcription	Esophagus	oesophagus
11	chr5:16656000-16657200	Weak transcription	NHDF-Ad	bronchial
12	chr5:16656200-16656400	Weak transcription	Hela-S3	cervix
13	chr5:16656200-16657000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr5:16656400-16656800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
15	chr5:16656400-16657000	Enhancers	Primary neutrophils fromperipheralblood	blood
16	chr5:16656400-16657200	Enhancers	HMEC	breast
17	chr5:16656400-16657800	Enhancers	Adipose Nuclei	Adipose
18	chr5:16656600-16657200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
19	chr5:16656600-16657200	Enhancers	Hela-S3	cervix
20	chr5:16656600-16658000	Enhancers	NHEK	skin
21	chr5:16656800-16657000	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
22	chr5:16656800-16657000	Enhancers	Fetal Brain Female	brain
23	chr5:16656800-16657000	Enhancers	Osteobl	bone
24	chr5:16656800-16657200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
25	chr5:16656800-16657200	Enhancers	Placenta	Placenta
26	chr5:16656800-16657400	Enhancers	Breast Myoepithelial Primary Cells	Breast
27	chr5:16657000-16657200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
28	chr5:16657000-16657600	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
29	chr5:16657000-16658200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr5:16657000-16664000	Weak transcription	Fetal Brain Female	brain
31	chr5:16657000-16665600	Weak transcription	Osteobl	bone
32	chr5:16657000-16668000	Weak transcription	Primary neutrophils fromperipheralblood	blood
33	chr5:16657200-16657400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
34	chr5:16657200-16657400	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
35	chr5:16657200-16657400	Enhancers	NHDF-Ad	bronchial
36	chr5:16657200-16660400	Weak transcription	Placenta	Placenta
37	chr5:16657200-16662800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
38	chr5:16657200-16663800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
39	chr5:16657200-16663800	Weak transcription	HMEC	breast
40	chr5:16657400-16658400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
41	chr5:16657400-16663200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
42	chr5:16657400-16664000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
43	chr5:16657400-16665600	Weak transcription	NHDF-Ad	bronchial
44	chr5:16657600-16658800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
45	chr5:16657800-16666600	Weak transcription	Adipose Nuclei	Adipose
46	chr5:16658000-16663800	Weak transcription	NHEK	skin
47	chr5:16658200-16670400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
48	chr5:16658400-16663600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
49	chr5:16658800-16659600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr5:16658800-16663400	Weak transcription	A549	lung

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