Variant report

Variant	nsv427709
Chromosome Location	chr5:8353876-8519855
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:807)
CpG islands
(count:673)
Chromatin interactive
region (count:41)
LncRNA
region (count:32)
Mature miRNA
region (count: 1)
miRNA target
sites (count:0)

(count:807 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:8456981-8457603	K562	blood:	n/a	n/a
2	ATF1	chr5:8457313-8457977	K562	blood:	n/a	n/a
3	ATF3	chr5:8457266-8457641	K562	blood:	n/a	n/a
4	ATF3	chr5:8457637-8457977	K562	blood:	n/a	n/a
5	ATF3	chr5:8457385-8457596	K562	blood:	n/a	n/a
6	BACH1	chr5:8457293-8458414	H1-hESC	embryonic stem cell:	n/a	chr5:8457494-8457508
7	BACH1	chr5:8457330-8458064	K562	blood:	n/a	chr5:8457494-8457508
8	BACH1	chr5:8466094-8466189	K562	blood:	n/a	n/a
9	BACH1	chr5:8354823-8354910	K562	blood:	n/a	chr5:8354847-8354861
10	BATF	chr5:8446312-8446635	GM12878	blood:	n/a	n/a
11	BCL11A	chr5:8435885-8436018	GM12878	blood:	n/a	n/a
12	BHLHE40	chr5:8456851-8458022	K562	blood:	n/a	n/a
13	BHLHE40	chr5:8474568-8474666	K562	blood:	n/a	n/a
14	BHLHE40	chr5:8457355-8458387	HepG2	liver:	n/a	n/a
15	BHLHE40	chr5:8458233-8458559	K562	blood:	n/a	n/a
16	BRCA1	chr5:8458210-8458271	Hela-S3	cervix:	n/a	n/a
17	BRCA1	chr5:8457088-8457928	Hela-S3	cervix:	n/a	n/a
18	CBX3	chr5:8457263-8457681	K562	blood:	n/a	n/a
19	CBX3	chr5:8456740-8458011	K562	blood:	n/a	n/a
20	CBX3	chr5:8470621-8470920	K562	blood:	n/a	n/a
21	CBX3	chr5:8470624-8470962	K562	blood:	n/a	n/a
22	CCNT2	chr5:8457339-8458513	K562	blood:	n/a	chr5:8458274-8458283
23	CEBPB	chr5:8413197-8413466	A549	lung:	n/a	chr5:8413335-8413346
24	CEBPB	chr5:8440231-8440301	HepG2	liver:	n/a	n/a
25	CEBPB	chr5:8486303-8486352	HepG2	liver:	n/a	n/a
26	CEBPB	chr5:8457327-8458568	Hela-S3	cervix:	n/a	n/a
27	CEBPB	chr5:8413227-8413457	HepG2	liver:	n/a	chr5:8413335-8413346
28	CEBPB	chr5:8426178-8426545	MCF-7	breast:	n/a	n/a
29	CEBPB	chr5:8457543-8457642	H1-hESC	embryonic stem cell:	n/a	n/a
30	CHD2	chr5:8457444-8457904	H1-hESC	embryonic stem cell:	n/a	n/a
31	CHD2	chr5:8457230-8458053	K562	blood:	n/a	n/a
32	CHD2	chr5:8457295-8458598	Hela-S3	cervix:	n/a	n/a
33	CREB1	chr5:8457414-8457696	A549	lung:	n/a	n/a
34	CREB1	chr5:8457294-8458014	H1-hESC	embryonic stem cell:	n/a	n/a
35	CREB1	chr5:8457340-8458133	HepG2	liver:	n/a	n/a
36	CREB1	chr5:8457331-8458097	K562	blood:	n/a	n/a
37	CTCF	chr5:8441602-8441657	HepG2	liver:	n/a	n/a
38	CTCF	chr5:8410969-8410971	MCF-7	breast:	n/a	n/a
39	CTCF	chr5:8395200-8395350	HepG2	liver:	n/a	n/a
40	CTCF	chr5:8395211-8395348	LNCaP	prostate:	n/a	n/a
41	CTCF	chr5:8426360-8426510	MCF-7	breast:	n/a	n/a
42	CTCF	chr5:8395200-8395350	NB4	blood:	n/a	n/a
43	CTCF	chr5:8474001-8474229	K562	blood:	n/a	n/a
44	CTCF	chr5:8474080-8474230	NHDF-neo	bronchial:	n/a	n/a
45	CTCF	chr5:8361567-8361595	ProgFib	skin:	n/a	n/a
46	CTCF	chr5:8474100-8474250	GM12869	blood:	n/a	n/a
47	CTCF	chr5:8479740-8479890	Hela-S3	cervix:	n/a	n/a
48	CTCF	chr5:8395160-8395310	A549	lung:	n/a	n/a
49	CTCF	chr5:8473960-8474110	GM12874	blood:	n/a	n/a
50	CTCF	chr5:8474120-8474270	NHLF	lung:	n/a	n/a

(count:673 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:8461041-8461091	NT2-D1	testis:	n/a
2	chr5:8457729-8457779	ProgFib	skin:	n/a
3	chr5:8461041-8461091	NT2-D1	testis:	n/a
4	chr5:8457729-8457779	ProgFib	skin:	n/a
5	chr5:8461832-8461882	HAEpiC	amniotic membrane:	n/a
6	chr5:8461832-8461882	BJ	skin:	n/a
7	chr5:8457548-8457598	SK-N-SH_RA	brain:	n/a
8	chr5:8458089-8458139	MCF-7	breast:	n/a
9	chr5:8457818-8457868	HAEpiC	amniotic membrane:	n/a
10	chr5:8456584-8456634	AoSMC	blood vessel:	n/a
11	chr5:8461832-8461882	NB4	blood:	n/a
12	chr5:8458089-8458139	ProgFib	skin:	n/a
13	chr5:8457548-8457598	HNPCEpiC	eye:	n/a
14	chr5:8461832-8461882	PrEC	prostate:	n/a
15	chr5:8457818-8457868	HIPEpiC	eye:	n/a
16	chr5:8457721-8457771	HCPEpiC	choroid plexus:	n/a
17	chr5:8457721-8457771	U87	brain:	n/a
18	chr5:8461041-8461091	HCT-116	colon:	n/a
19	chr5:8457818-8457868	AoSMC	blood vessel:	n/a
20	chr5:8461832-8461882	HRCEpiC	kidney:	n/a
21	chr5:8461832-8461882	RPTEC	kidney:	n/a
22	chr5:8461832-8461882	K562	blood:	n/a
23	chr5:8457970-8458020	HepG2	liver:	n/a
24	chr5:8462139-8462189	NH-A	brain:	n/a
25	chr5:8458089-8458139	SK-N-SH	brain:	n/a
26	chr5:8457818-8457868	NHDF-neo	bronchial:	n/a
27	chr5:8456584-8456634	GM12892	blood:	n/a
28	chr5:8457729-8457779	H1-hESC	embryonic stem cell:	embryo
29	chr5:8457548-8457598	NH-A	brain:	n/a
30	chr5:8458392-8458442	Jurkat	blood:	n/a
31	chr5:8457721-8457771	ECC-1	luminal epithelium:	n/a
32	chr5:8462139-8462189	ECC-1	luminal epithelium:	n/a
33	chr5:8456584-8456634	PANC-1	pancreas:	n/a
34	chr5:8456584-8456634	HCPEpiC	choroid plexus:	n/a
35	chr5:8458089-8458139	RPTEC	kidney:	n/a
36	chr5:8461832-8461882	U87	brain:	n/a
37	chr5:8461041-8461091	HAEpiC	amniotic membrane:	n/a
38	chr5:8457721-8457771	HMEC	breast:	n/a
39	chr5:8458089-8458139	HCM	heart:	n/a
40	chr5:8461041-8461091	HCF	heart:	n/a
41	chr5:8457970-8458020	GM19239	blood:	n/a
42	chr5:8457729-8457779	NB4	blood:	n/a
43	chr5:8457721-8457771	HL-60	blood:	n/a
44	chr5:8456584-8456634	HPAEpiC	pulmonary alveolar:	n/a
45	chr5:8458392-8458442	A549	lung:	n/a
46	chr5:8457818-8457868	ECC-1	luminal epithelium:	n/a
47	chr5:8457818-8457868	SK-N-SH_RA	brain:	n/a
48	chr5:8457729-8457779	SK-N-MC	brain:	n/a
49	chr5:8457729-8457779	GM19239	blood:	n/a
50	chr5:8456584-8456634	HIPEpiC	eye:	n/a

(count:41 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr17:41463656..41466177-chr5:8424542..8427523,2	MCF-7	breast:
2	chr17:41398647..41403327-chr5:8424523..8427522,6	K562	blood:
3	chr20:44563204..44564063-chr5:8461812..8462367,2	Hela-S3	cervix:
4	chr5:8247458..8248066-chr5:8425960..8426700,2	MCF-7	breast:
5	chr5:8436070..8438257-chr5:8440471..8442267,2	K562	blood:
6	chr5:8457078..8459207-chr5:8461943..8464823,4	K562	blood:
7	chr5:8247316..8248146-chr5:8426139..8426948,3	MCF-7	breast:
8	chr5:8456789..8458556-chr5:8461393..8463555,2	MCF-7	breast:
9	chr5:8384067..8386100-chr5:8387873..8389491,2	K562	blood:
10	chr5:8428561..8430944-chr5:8432470..8435197,2	MCF-7	breast:
11	chr5:8455948..8459329-chr5:8460368..8463674,5	K562	blood:
12	chr5:8462445..8464940-chr5:8473267..8475894,2	K562	blood:
13	chr17:41380556..41383320-chr5:8424542..8426042,2	K562	blood:
14	chr5:8456935..8459076-chr5:8488179..8490717,2	K562	blood:
15	chr5:8461759..8464771-chr5:8466218..8469670,3	K562	blood:
16	chr5:8486955..8488830-chr5:8517823..8520241,2	MCF-7	breast:
17	chr5:8451906..8454974-chr5:8455165..8458746,3	K562	blood:
18	chr5:8462445..8464940-chr5:8473267..8475894,2	K562	blood:
19	chr5:8326714..8328797-chr5:8452465..8455003,2	K562	blood:
20	chr5:8507041..8510012-chr5:8511674..8514146,2	K562	blood:
21	chr17:36002985..36003673-chr5:8457586..8458291,2	Hela-S3	cervix:
22	chr5:8461759..8464771-chr5:8466218..8469670,3	K562	blood:
23	chr5:8455618..8458508-chr5:8467454..8469231,2	MCF-7	breast:
24	chr5:8340161..8341518-chr5:8426060..8426931,4	MCF-7	breast:
25	chr5:8507041..8510012-chr5:8511674..8514146,2	K562	blood:
26	chr5:8435771..8437570-chr5:8440279..8442267,2	K562	blood:
27	chr5:8435771..8437570-chr5:8440279..8442267,2	K562	blood:
28	chr5:8424954..8426951-chr5:8459409..8461933,2	K562	blood:
29	chr5:8472940..8473440-chr7:72649624..72650127,2	Hela-S3	cervix:
30	chr5:8486955..8488830-chr5:8517823..8520241,2	MCF-7	breast:
31	chr5:8428561..8430944-chr5:8432470..8435197,2	MCF-7	breast:
32	chr5:8384067..8386100-chr5:8387873..8389491,2	K562	blood:
33	chr5:8340568..8341488-chr5:8395221..8395752,2	MCF-7	breast:
34	chr5:8436070..8438257-chr5:8440471..8442267,2	K562	blood:
35	chr5:8383168..8386100-chr5:8387532..8389491,3	K562	blood:
36	chr5:7927628..7928513-chr5:8394887..8395661,2	MCF-7	breast:
37	chr5:8383168..8386100-chr5:8387532..8389491,3	K562	blood:
38	chr17:41380454..41382056-chr5:8424522..8426042,2	K562	blood:
39	chr11:62608642..62609503-chr5:8457394..8458109,3	Hela-S3	cervix:
40	chr17:41463804..41465376-chr5:8424543..8427523,2	K562	blood:
41	chr5:8455948..8459329-chr5:8460368..8463674,5	K562	blood:

(count:32 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FASTKD3-1	chr5:8452336-8452393	ENSG00000245729
2	lnc-FASTKD3-1	chr5:8446156-8446468	NONHSAT100287
3	lnc-SEMA5A-11	chr5:8456059-8456671	NONHSAT100289
4	lnc-FASTKD3-1	chr5:8457562-8457645	ENSG00000249159.2
5	lnc-FASTKD3-1	chr5:8457562-8457677	NONHSAT100283
6	lnc-FASTKD3-1	chr5:8433968-8434085	ENSG00000249159
7	lnc-FASTKD3-5	chr5:8410902-8411109	NONHSAT100286
8	lnc-FASTKD3-1	chr5:8452336-8452393	ENSG00000249159
9	lnc-FASTKD3-1	chr5:8452336-8452393	NONHSAT100283
10	lnc-FASTKD3-6	chr5:8445062-8445648	ENSG00000272049.1
11	lnc-FASTKD3-1	chr5:8390294-8390408	ucscGeneNc_uc003jeh_1
12	lnc-FASTKD3-1	chr5:8505336-8505393	ucscGeneNc_uc003jeh_1
13	lnc-FASTKD3-1	chr5:8387751-8387822	ENSG00000249159
14	lnc-FASTKD3-1	chr5:8510562-8510671	ucscGeneNc_uc003jeh_1
15	lnc-MTRR-3	chr5:8460046-8460209	NONHSAT100288
16	lnc-FASTKD3-1	chr5:8386596-8387565	ucscGeneNc_uc003jeh_1
17	lnc-FASTKD3-1	chr5:8387691-8387839	ucscGeneNc_uc003jeh_1
18	lnc-FASTKD3-1	chr5:8457562-8457688	NONHSAT100287
19	lnc-FASTKD3-1	chr5:8446214-8446468	ENSG00000249159.2
20	lnc-FASTKD3-1	chr5:8387640-8387822	ENSG00000245729
21	lnc-FASTKD3-1	chr5:8457562-8457677	ENSG00000249159
22	lnc-FASTKD3-1	chr5:8452336-8452393	NONHSAT100287
23	lnc-FASTKD3-1	chr5:8457562-8457671	ENSG00000245729
24	lnc-FASTKD3-1	chr5:8387640-8387822	NONHSAT100283
25	lnc-SEMA5A-10	chr5:8460226-8460932	NONHSAT100292
26	lnc-MTRR-3	chr5:8450856-8451757	NONHSAT100288
27	lnc-FASTKD3-1	chr5:8433186-8433261	ENSG00000249159
28	lnc-FASTKD3-1	chr5:8440640-8440822	ucscGeneNc_uc003jeh_1
29	lnc-MTRR-11	chr5:8458955-8459296	NONHSAT100291
30	lnc-MTRR-12	chr5:8510804-8510879	ucscGeneNc_uc003jei_2
31	lnc-FASTKD3-1	chr5:8452336-8452393	ENSG00000249159.2
32	lnc-MTRR-12	chr5:8513046-8516208	ucscGeneNc_uc003jei_2

miRNA name	Chromosome Location	mirBase accession
hsa-miR-4458	chr5:8461046-8461064	MIMAT0018980

No data

Variant related genes	Relation type
ENSG00000245729	TF binding region
ENSG00000250037	TF binding region
MIR4458HG	TF binding region
ENSG00000249159	TF binding region
ENSG00000251549	TF binding region
ENSG00000272049	TF binding region
ENSG00000245729	CpG island
ENSG00000250037	CpG island
MIR4458HG	CpG island
ENSG00000249159	CpG island
ENSG00000251549	CpG island
ENSG00000272049	CpG island
ENSG00000250037	chromatin interactions
ENSG00000236383	chromatin interactions
ENSG00000245729	chromatin interactions
ENSG00000133316	chromatin interactions
ENSG00000267668	chromatin interactions
ENSG00000100982	chromatin interactions
ENSG00000141141	chromatin interactions
ENSG00000188825	chromatin interactions
ENSG00000249159	chromatin interactions
ENSG00000247516	chromatin interactions
EIF4G2	miRNA target sites
ARHGAP12	miRNA target sites

Extended variants
information (count: 4679 )
Associated
traits (count: 105 )

Variant overlapped rSNPs/rCNVs (count:4679 , 50 per page) page: 1 2 3 4 5 6 7 ... 94

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs551417821	chr5:8354221-8354222	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
2	rs141434630	chr5:8354255-8354256	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs113795747	chr5:8354256-8354257	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs182938605	chr5:8354270-8354271	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs547825046	chr5:8354273-8354274	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs567923898	chr5:8354290-8354291	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs188006537	chr5:8354296-8354297	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs367948430	chr5:8354313-8354314	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs192479787	chr5:8354341-8354342	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs569638956	chr5:8354353-8354354	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs79350103	chr5:8354368-8354369	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs558644386	chr5:8354371-8354372	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs534746673	chr5:8354373-8354374	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs13158614	chr5:8354441-8354442	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs77191546	chr5:8354472-8354473	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs554602533	chr5:8354493-8354494	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs574692445	chr5:8354514-8354515	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs543325338	chr5:8354534-8354535	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs113499592	chr5:8354625-8354626	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs531560148	chr5:8354672-8354673	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs545140366	chr5:8354766-8354767	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs565038566	chr5:8354781-8354782	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs527909697	chr5:8354825-8354826	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs115443075	chr5:8354861-8354862	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs184523777	chr5:8354864-8354865	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs530443167	chr5:8354882-8354883	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs116078536	chr5:8354883-8354884	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs114851881	chr5:8354946-8354947	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs538628474	chr5:8354990-8354991	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs114620427	chr5:8355819-8355820	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs192164690	chr5:8355844-8355845	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs573109835	chr5:8355948-8355949	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs530095956	chr5:8355956-8355957	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs572301479	chr5:8355980-8355981	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs541521729	chr5:8355990-8355991	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs561214473	chr5:8356044-8356045	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs575023036	chr5:8356123-8356124	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs146933818	chr5:8356297-8356298	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs548801883	chr5:8356327-8356328	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs564005047	chr5:8356339-8356340	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs570147950	chr5:8356363-8356364	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs531262159	chr5:8356369-8356370	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs552858327	chr5:8356385-8356386	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs563189124	chr5:8356435-8356436	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs559311515	chr5:8356461-8356462	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs11950781	chr5:8356475-8356476	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs137871613	chr5:8356527-8356528	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs568044220	chr5:8356578-8356579	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs530654737	chr5:8356579-8356580	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs184937314	chr5:8356715-8356716	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:105)

Disease	PMID	Source
Sudden cardiac death	19188705	CNVD
renal disease	17924346	CNVD
Cervical squamous cell carcinoma	21590768	CNVD
abnormal development	18461090	CNVD
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
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
T-cell prolymphocytic leukemia	17713554	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
low-grade B-cell lymphoma tumor	18367492	CNVD
Multiple myeloma	17550852	CNVD
Developmental delay	21147756	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
Melanoma	22183965	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
lymphocytic leukemia	21291569	CNVD
Autism	22495311	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	16608533	CNVD
Anaplastic large cell lymphoma	18179710	CNVD
Urothelial carcinoma	21177765	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Melanoma	18172304	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Ovarian cancer	19193619	CNVD
Hepatocellular carcinoma	16785998	CNVD
Cancer	22183965	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Intellectual disability	22102821	CNVD
Myelofibrosis	22110671	CNVD
Cri-du chat syndrome	16773131	CNVD
Cryptorchidism	21048976	CNVD
Glioblastoma multiforme	22286061	CNVD
Cervical cancer	16585170	CNVD
Mental retardation	16773131	CNVD
Non-small cell lung cancer	21829676	CNVD
Cri-du chat syndrome	22470819	CNVD
sporadic birth defects	19047251	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:699 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:8354200-8354400	ZNF genes & repeats	Pancreas	Pancrea
2	chr5:8354400-8355000	Weak transcription	Pancreas	Pancrea
3	chr5:8355800-8356600	Enhancers	Brain Cingulate Gyrus	brain
4	chr5:8356400-8357000	Enhancers	Brain Anterior Caudate	brain
5	chr5:8356600-8357000	Enhancers	Brain Inferior Temporal Lobe	brain
6	chr5:8362800-8363600	Enhancers	Pancreatic Islets	Pancreatic Islet
7	chr5:8362800-8363800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
8	chr5:8363000-8363600	Enhancers	NH-A	brain
9	chr5:8363200-8363600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr5:8363200-8363800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr5:8363400-8363800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
12	chr5:8363600-8366400	Weak transcription	Pancreatic Islets	Pancreatic Islet
13	chr5:8366000-8367200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
14	chr5:8366200-8366600	Active TSS	Brain Angular Gyrus	brain
15	chr5:8366200-8366600	Active TSS	Brain Cingulate Gyrus	brain
16	chr5:8366200-8366800	Active TSS	Brain Hippocampus Middle	brain
17	chr5:8366200-8366800	Active TSS	Brain Substantia Nigra	brain
18	chr5:8366200-8367200	Enhancers	Cortex derived primary cultured neurospheres	brain
19	chr5:8366200-8367200	Active TSS	Brain Inferior Temporal Lobe	brain
20	chr5:8366200-8367400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
21	chr5:8366200-8367600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr5:8366400-8366800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr5:8366400-8366800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr5:8366400-8366800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
25	chr5:8366400-8366800	Active TSS	Brain Anterior Caudate	brain
26	chr5:8366600-8367200	Weak transcription	Brain Cingulate Gyrus	brain
27	chr5:8366800-8367200	Enhancers	Brain Substantia Nigra	brain
28	chr5:8366800-8367600	Enhancers	Brain Hippocampus Middle	brain
29	chr5:8367000-8367400	Enhancers	Brain Anterior Caudate	brain
30	chr5:8367200-8367400	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
31	chr5:8367200-8367600	Enhancers	Brain Cingulate Gyrus	brain
32	chr5:8367200-8367600	Enhancers	Fetal Lung	lung
33	chr5:8367400-8367600	Enhancers	Brain Inferior Temporal Lobe	brain
34	chr5:8367400-8368400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
35	chr5:8367600-8375600	Weak transcription	Fetal Lung	lung
36	chr5:8368400-8368600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
37	chr5:8375600-8376000	Enhancers	Fetal Lung	lung
38	chr5:8376400-8377000	Enhancers	Dnd41	blood
39	chr5:8380000-8380200	Enhancers	Cortex derived primary cultured neurospheres	brain
40	chr5:8380000-8380200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
41	chr5:8380200-8382200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
42	chr5:8381000-8381400	Enhancers	Liver	Liver
43	chr5:8382200-8384400	Enhancers	Cortex derived primary cultured neurospheres	brain
44	chr5:8382200-8384600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
45	chr5:8382400-8384000	Enhancers	Fetal Brain Female	brain
46	chr5:8382400-8384400	Enhancers	Brain Germinal Matrix	brain
47	chr5:8382600-8383400	Enhancers	Pancreatic Islets	Pancreatic Islet
48	chr5:8382600-8383800	Enhancers	Fetal Lung	lung
49	chr5:8382600-8384000	Enhancers	NHDF-Ad	bronchial
50	chr5:8382600-8384400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin

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