Variant report

Variant	nsv900562
Chromosome Location	chr13:76072743-76176680
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2036)
CpG islands
(count:1955)
Chromatin interactive
region (count:64)
LncRNA
region (count:10)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:2036 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr13:76111988-76112275	K562	blood:	n/a	n/a
2	ARID3A	chr13:76111847-76112381	HepG2	liver:	n/a	n/a
3	ARID3A	chr13:76123347-76124671	HepG2	liver:	n/a	n/a
4	ARID3A	chr13:76104571-76105292	HepG2	liver:	n/a	n/a
5	ARID3A	chr13:76140823-76141209	HepG2	liver:	n/a	n/a
6	ARID3A	chr13:76140888-76140979	K562	blood:	n/a	n/a
7	ARID3A	chr13:76119103-76119402	HepG2	liver:	n/a	n/a
8	ARID3A	chr13:76123487-76124101	K562	blood:	n/a	n/a
9	ATF1	chr13:76115164-76115846	K562	blood:	n/a	n/a
10	ATF2	chr13:76086299-76086714	GM12878	blood:	n/a	n/a
11	ATF2	chr13:76123176-76123915	GM12878	blood:	n/a	n/a
12	ATF2	chr13:76123258-76124165	GM12878	blood:	n/a	n/a
13	ATF2	chr13:76088550-76089058	GM12878	blood:	n/a	n/a
14	ATF2	chr13:76161744-76162155	H1-hESC	embryonic stem cell:	n/a	n/a
15	ATF2	chr13:76111559-76112389	GM12878	blood:	n/a	n/a
16	ATF2	chr13:76112008-76112514	H1-hESC	embryonic stem cell:	n/a	n/a
17	ATF2	chr13:76161743-76162267	H1-hESC	embryonic stem cell:	n/a	n/a
18	ATF2	chr13:76086245-76086999	GM12878	blood:	n/a	n/a
19	ATF3	chr13:76124408-76124734	K562	blood:	n/a	n/a
20	BACH1	chr13:76111716-76112543	H1-hESC	embryonic stem cell:	n/a	n/a
21	BACH1	chr13:76123150-76123218	K562	blood:	n/a	n/a
22	BACH1	chr13:76130079-76130395	K562	blood:	n/a	n/a
23	BACH1	chr13:76123391-76124432	H1-hESC	embryonic stem cell:	n/a	n/a
24	BACH1	chr13:76152548-76152550	K562	blood:	n/a	n/a
25	BACH1	chr13:76123468-76123932	K562	blood:	n/a	n/a
26	BATF	chr13:76079141-76079398	GM12878	blood:	n/a	chr13:76079240-76079251
27	BATF	chr13:76123360-76123696	GM12878	blood:	n/a	n/a
28	BATF	chr13:76153753-76153938	GM12878	blood:	n/a	n/a
29	BATF	chr13:76153723-76153987	GM12878	blood:	n/a	n/a
30	BATF	chr13:76086423-76086754	GM12878	blood:	n/a	n/a
31	BATF	chr13:76079101-76079335	GM12878	blood:	n/a	chr13:76079240-76079251
32	BATF	chr13:76086386-76086750	GM12878	blood:	n/a	n/a
33	BCL3	chr13:76112015-76112538	A549	lung:	n/a	n/a
34	BCLAF1	chr13:76111591-76112186	GM12878	blood:	n/a	n/a
35	BCLAF1	chr13:76123288-76124229	GM12878	blood:	n/a	n/a
36	BCLAF1	chr13:76123254-76124297	GM12878	blood:	n/a	n/a
37	BCLAF1	chr13:76086159-76086806	GM12878	blood:	n/a	n/a
38	BHLHE40	chr13:76111845-76112497	K562	blood:	n/a	n/a
39	BHLHE40	chr13:76111942-76112433	A549	lung:	n/a	n/a
40	BHLHE40	chr13:76123174-76124311	GM12878	blood:	n/a	n/a
41	BHLHE40	chr13:76123495-76124021	A549	lung:	n/a	n/a
42	BHLHE40	chr13:76111626-76112484	HepG2	liver:	n/a	n/a
43	BHLHE40	chr13:76111540-76112825	GM12878	blood:	n/a	n/a
44	BHLHE40	chr13:76123316-76124079	K562	blood:	n/a	n/a
45	BHLHE40	chr13:76123284-76124344	HepG2	liver:	n/a	n/a
46	BHLHE40	chr13:76130055-76130270	K562	blood:	n/a	n/a
47	BRCA1	chr13:76153639-76153677	Hela-S3	cervix:	n/a	n/a
48	BRCA1	chr13:76111647-76112440	HepG2	liver:	n/a	n/a
49	BRCA1	chr13:76123401-76123970	Hela-S3	cervix:	n/a	n/a
50	BRCA1	chr13:76123474-76123899	HepG2	liver:	n/a	n/a

(count:1955 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:76112039-76112089	PrEC	prostate:	n/a
2	chr13:76112232-76112282	T-47D	breast:	n/a
3	chr13:76123904-76123954	Hepatocyte	liver:	n/a
4	chr13:76112039-76112089	PrEC	prostate:	n/a
5	chr13:76112232-76112282	T-47D	breast:	n/a
6	chr13:76123904-76123954	Hepatocyte	liver:	n/a
7	chr13:76111918-76111968	PFSK-1	brain:	n/a
8	chr13:76109220-76109270	AG10803	skin:	n/a
9	chr13:76123781-76123831	MCF10A-Er-Src	breast:	n/a
10	chr13:76112232-76112282	AG10803	skin:	n/a
11	chr13:76122768-76122818	PFSK-1	brain:	n/a
12	chr13:76112973-76113023	BJ	skin:	n/a
13	chr13:76111980-76112030	HIPEpiC	eye:	n/a
14	chr13:76119663-76119713	NHBE	bronchial:	n/a
15	chr13:76123901-76123951	HepG2	liver:	n/a
16	chr13:76123853-76123903	HMEC	breast:	n/a
17	chr13:76112030-76112080	T-47D	breast:	n/a
18	chr13:76109220-76109270	ProgFib	skin:	n/a
19	chr13:76115526-76115576	HRCEpiC	kidney:	n/a
20	chr13:76124267-76124317	PFSK-1	brain:	n/a
21	chr13:76112039-76112089	AG04450	lung:	fetal
22	chr13:76111918-76111968	HCM	heart:	n/a
23	chr13:76123901-76123951	A549	lung:	n/a
24	chr13:76111751-76111801	HEK293	kidney:	embryo
25	chr13:76111785-76111835	SAEC	small airway:	n/a
26	chr13:76123904-76123954	AG04449	skin:	fetal
27	chr13:76124424-76124474	HEEpiC	esophagus:	n/a
28	chr13:76111107-76111157	HCF	heart:	n/a
29	chr13:76115526-76115576	Jurkat	blood:	n/a
30	chr13:76111785-76111835	GM06990	blood:	n/a
31	chr13:76112039-76112089	NHDF-neo	bronchial:	n/a
32	chr13:76123478-76123528	Caco-2	colon:	n/a
33	chr13:76124424-76124474	Caco-2	colon:	n/a
34	chr13:76112232-76112282	AG04449	skin:	fetal
35	chr13:76112980-76113030	NB4	blood:	n/a
36	chr13:76099592-76099642	AG04450	lung:	fetal
37	chr13:76111918-76111968	NHBE	bronchial:	n/a
38	chr13:76109220-76109270	NHBE	bronchial:	n/a
39	chr13:76112187-76112237	HepG2	liver:	n/a
40	chr13:76092702-76092752	HCM	heart:	n/a
41	chr13:76111980-76112030	BE2_C	brain:	n/a
42	chr13:76115526-76115576	PFSK-1	brain:	n/a
43	chr13:76111751-76111801	NHDF-neo	bronchial:	n/a
44	chr13:76112030-76112080	PrEC	prostate:	n/a
45	chr13:76123895-76123945	Jurkat	blood:	n/a
46	chr13:76128081-76128131	SK-N-MC	brain:	n/a
47	chr13:76123478-76123528	HRCEpiC	kidney:	n/a
48	chr13:76111107-76111157	HepG2	liver:	n/a
49	chr13:76111751-76111801	BE2_C	brain:	n/a
50	chr13:76112232-76112282	Hepatocyte	liver:	n/a

(count:64 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr13:76152309..76155041-chr13:76158108..76159629,2	K562	blood:
2	chr13:76124076..76125593-chr13:76162284..76165016,2	K562	blood:
3	chr13:76124018..76125732-chr13:76125795..76127481,2	MCF-7	breast:
4	chr13:76115839..76118347-chr13:76129572..76131579,2	K562	blood:
5	chr13:76102775..76109881-chr13:76110381..76113047,9	MCF-7	breast:
6	chr13:76123621..76124364-chrX:134654253..134654910,2	NB4	blood:
7	chr13:76106394..76109955-chr13:76110419..76113939,6	MCF-7	breast:
8	chr13:76055919..76057695-chr13:76110507..76112437,2	MCF-7	breast:
9	chr13:76115839..76118347-chr13:76129572..76131579,2	K562	blood:
10	chr13:75946802..75947592-chr13:76121701..76122528,2	MCF-7	breast:
11	chr13:76074143..76076070-chr13:76123601..76125267,2	MCF-7	breast:
12	chr13:76055434..76058277-chr13:76123047..76126766,3	K562	blood:
13	chr13:76080347..76082551-chr13:76083582..76085785,4	K562	blood:
14	chr13:76107791..76110428-chr13:76144234..76145882,2	K562	blood:
15	chr1:151253613..151254502-chr13:76111700..76112352,2	Hela-S3	cervix:
16	chr13:76111404..76112078-chr17:26989037..26989702,2	Hela-S3	cervix:
17	chr13:76055248..76057886-chr13:76110224..76112780,4	MCF-7	breast:
18	chr13:76075450..76077905-chr13:76087329..76089009,2	K562	blood:
19	chr13:76111452..76114150-chr13:76122087..76125338,6	MCF-7	breast:
20	chr13:76122653..76127194-chr13:76130432..76132318,4	MCF-7	breast:
21	chr13:76107791..76110428-chr13:76144234..76145882,2	K562	blood:
22	chr13:76076405..76080634-chr13:76083700..76088829,4	K562	blood:
23	chr13:76109717..76113590-chr13:76122029..76126081,5	MCF-7	breast:
24	chr13:76153049..76155664-chr13:76161169..76162949,2	K562	blood:
25	chr13:76101020..76103303-chr13:76108939..76111291,2	K562	blood:
26	chr13:76123475..76126296-chr13:76136199..76138617,2	MCF-7	breast:
27	chr13:75931707..75932464-chr13:76077700..76078200,2	MCF-7	breast:
28	chr13:76101020..76103303-chr13:76108939..76111291,2	K562	blood:
29	chr13:76160277..76161808-chr13:76162172..76164407,2	K562	blood:
30	chr13:76109113..76111805-chr13:76112674..76114626,2	K562	blood:
31	chr13:76109687..76114004-chr13:76118514..76122227,3	K562	blood:
32	chr13:76143405..76146053-chr13:76147700..76149492,2	K562	blood:
33	chr13:76056169..76056921-chr13:76123095..76123971,5	MCF-7	breast:
34	chr13:76110734..76112526-chr13:76124795..76127675,2	K562	blood:
35	chr13:76080347..76082551-chr13:76083582..76085785,4	K562	blood:
36	chr13:76141660..76144515-chr13:76144732..76146608,2	MCF-7	breast:
37	chr13:76075450..76077905-chr13:76087329..76089009,2	K562	blood:
38	chr13:76124376..76126025-chr13:76132730..76134454,2	K562	blood:
39	chr13:76101122..76104303-chr13:76108576..76110569,3	K562	blood:
40	chr13:76111859..76112746-chr13:76123326..76123936,2	MCF-7	breast:
41	chr13:76152309..76155041-chr13:76158108..76159629,2	K562	blood:
42	chr13:76111452..76114150-chr13:76122087..76125338,6	MCF-7	breast:
43	chr13:76095939..76098463-chr13:76110881..76113865,2	MCF-7	breast:
44	chr13:76074591..76077298-chr13:76079207..76081950,2	K562	blood:
45	chr13:76102775..76109881-chr13:76110381..76113047,9	MCF-7	breast:
46	chr13:76111859..76112746-chr13:76123326..76123936,2	MCF-7	breast:
47	chr13:76118168..76119687-chr13:76122527..76125250,2	MCF-7	breast:
48	chr13:76123894..76126209-chr13:76129145..76131618,3	K562	blood:
49	chr13:76124018..76125732-chr13:76125795..76127481,2	MCF-7	breast:
50	chr13:76124076..76125593-chr13:76162284..76165016,2	K562	blood:

(count:10 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LMO7-2	chr13:76140968-76140987	ENSG00000261553.1
2	lnc-TBC1D4-2	chr13:76123459-76123575	NONHSAT034360
3	lnc-TBC1D4-2	chr13:76111635-76111811	NONHSAT034360
4	lnc-LMO7-2	chr13:76169051-76169126	ENSG00000261553.1
5	lnc-LMO7-2	chr13:76141363-76141448	ENSG00000261553.1
6	lnc-TBC1D4-2	chr13:76104250-76104402	NONHSAT034360
7	lnc-COMMD6-4	chr13:76140115-76140230	l_873_chr13:76072523-76201534_testes
8	lnc-COMMD6-4	chr13:76072524-76072824	l_873_chr13:76072523-76201534_testes
9	lnc-COMMD6-4	chr13:76161358-76161715	l_873_chr13:76072523-76201534_testes
10	lnc-LMO7-2	chr13:76143596-76143643	ENSG00000261553.1

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	COMMD6	hsa-miR-106b-5p	chr13:76100615-76100635

Variant related genes	Relation type
COMMD6	TF binding region
ENSG00000261553	TF binding region
UCHL3	TF binding region
COMMD6	CpG island
ENSG00000261553	CpG island
UCHL3	CpG island
ENSG00000136111	chromatin interactions
ENSG00000176973	chromatin interactions
ENSG00000109111	chromatin interactions
ENSG00000165359	chromatin interactions
ENSG00000261553	chromatin interactions
ENSG00000232671	chromatin interactions
ENSG00000225235	chromatin interactions
ENSG00000143373	chromatin interactions
ENSG00000188243	chromatin interactions
ENSG00000118939	chromatin interactions
ENSG00000132581	chromatin interactions
ENSG00000230590	chromatin interactions

Extended variants
information (count: 3738 )
Associated
traits (count: 96 )

Variant overlapped rSNPs/rCNVs (count:3738 , 50 per page) page: 1 2 3 4 5 6 7 ... 75

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4885301	chr13:76072743-76072744	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs545119558	chr13:76072770-76072771	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
3	rs80260934	chr13:76072773-76072774	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
4	rs79498682	chr13:76072804-76072805	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
5	rs9573571	chr13:76072820-76072821	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs35554364	chr13:76073872-76073873	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs193216686	chr13:76073874-76073875	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs564902309	chr13:76073960-76073961	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs532337346	chr13:76073962-76073963	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs551543030	chr13:76073964-76073965	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs566960462	chr13:76073995-76073996	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs11616881	chr13:76074057-76074058	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs527831787	chr13:76074088-76074089	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs184937776	chr13:76074089-76074090	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs187390565	chr13:76074148-76074149	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs371676164	chr13:76074153-76074154	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs538125262	chr13:76074164-76074165	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs192128815	chr13:76074239-76074240	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs147699715	chr13:76074241-76074242	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs17064571	chr13:76074247-76074248	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs1323691	chr13:76074273-76074274	Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
22	rs9573572	chr13:76074291-76074292	Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs78048570	chr13:76074293-76074294	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs535970909	chr13:76074297-76074298	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs546228550	chr13:76074304-76074305	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs116153681	chr13:76074328-76074329	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs118177827	chr13:76074341-76074342	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs565193963	chr13:76074352-76074353	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs139388257	chr13:76074365-76074366	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs11373574	chr13:76074374-76074375	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs577102263	chr13:76074520-76074521	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs541216301	chr13:76074534-76074535	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs559613766	chr13:76074535-76074536	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs569417534	chr13:76074549-76074550	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs527767979	chr13:76074590-76074591	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs1570539	chr13:76074634-76074635	Inactive region	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs1570540	chr13:76074714-76074715	Inactive region	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs531737145	chr13:76074722-76074723	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs550169451	chr13:76074756-76074757	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs189764947	chr13:76074768-76074769	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs375820414	chr13:76074787-76074788	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs539012260	chr13:76074834-76074835	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs1570541	chr13:76074865-76074866	Inactive region	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs79854739	chr13:76074899-76074900	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs377410244	chr13:76074932-76074933	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs554247217	chr13:76074983-76074984	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs534281795	chr13:76074984-76074985	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs9543949	chr13:76075013-76075014	Inactive region	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs537039511	chr13:76075023-76075024	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs142611123	chr13:76075089-76075090	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:96)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
HIV/AIDS	22032296	CNVD
Prostate cancer	16705090	CNVD
High-proliferative meningiomas	17937814	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Autism	22495311	CNVD
Chordoma	21602918	CNVD
Bladder cancer	21949216	CNVD
Acute myeloid leukemia	16864856	CNVD
Burkitt''s lymphoma	18698080	CNVD
Cancer	21637783	CNVD
Medulloblastoma	21979893	CNVD
Chronic lymphocytic leukemia	21518781	CNVD
colon cancer	17210682	CNVD
Endometrial cancer	22040021	CNVD
Colorectal cancer	20709793	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Ovarian cancer	20844748	CNVD
Colorectal cancer	19359472	CNVD
Intracranial aneurysm	19064780	CNVD
Breast cancer	19287154	CNVD
Acute myeloid leukemia	18379011	CNVD
Human rectal carcinomas	16397240	CNVD
Olfactory neuroblastoma	18408657	CNVD
Multiple myeloma	17077331	CNVD
Ependymoma	16718352	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Colorectal cancer	16272173	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Ovarian cancer	22174824	CNVD
Breast cancer	17133270	CNVD
Myoepithelioma	18604193	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Paraganglioma	21461997	CNVD
Pheochromocytoma	21461997	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Prostate cancer	18632612	CNVD
Colorectal cancer	21586687	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Retinoblastoma	19183342	CNVD
Developmental delay	21147756	CNVD
Melanoma	18172304	CNVD
Prostate cancer	16573809	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Basal cell lymphoma	17053054	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
lymphocytic leukemia	21291569	CNVD
Breast cancer	21858162	CNVD
Metanephric adenoma	20802469	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Gastric cancer	17908304	CNVD
Breast cancer	17393978	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Liposarcoma	21253554	CNVD
Colorectal cancer	16774939	CNVD
Adenoid cystic carcinoma	17372589	CNVD
abnormal development	18461090	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal cancer	21851588	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Hirschsprung''s Disease	21712996	CNVD
Prostate cancer	21965145	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Intracranial aneurysm	16715129	CNVD
Non-small cell lung cancer	19010865	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Prostate cancer	22341455	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:2823 , 50 per page) page: 1 2 3 4 5 6 7 ... 57

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:76073800-76074600	Enhancers	Fetal Brain Female	brain
2	chr13:76078400-76079200	Enhancers	Monocytes-CD14+_RO01746	blood
3	chr13:76078400-76082600	Enhancers	Primary monocytes fromperipheralblood	blood
4	chr13:76079000-76080800	Enhancers	Primary neutrophils fromperipheralblood	blood
5	chr13:76079000-76082600	Enhancers	Primary hematopoietic stem cells short term culture	blood
6	chr13:76079200-76080000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
7	chr13:76079200-76080000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr13:76079200-76080000	Enhancers	Placenta	Placenta
9	chr13:76079200-76080000	Enhancers	GM12878-XiMat	blood
10	chr13:76079200-76080400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
11	chr13:76079600-76082200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
12	chr13:76080400-76083200	Enhancers	Monocytes-CD14+_RO01746	blood
13	chr13:76080800-76081200	Weak transcription	Primary neutrophils fromperipheralblood	blood
14	chr13:76081000-76081600	Enhancers	Skeletal Muscle Female	skeletal muscle
15	chr13:76081200-76081400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr13:76081200-76081600	Enhancers	HMEC	breast
17	chr13:76081200-76081800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
18	chr13:76081200-76082000	Enhancers	Skeletal Muscle Male	skeletal muscle
19	chr13:76081200-76082200	Enhancers	Fetal Muscle Leg	muscle
20	chr13:76081200-76082600	Enhancers	Psoas Muscle	Psoas
21	chr13:76081200-76083200	Enhancers	Breast Myoepithelial Primary Cells	Breast
22	chr13:76081200-76083400	Enhancers	Primary neutrophils fromperipheralblood	blood
23	chr13:76081400-76081600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
24	chr13:76081400-76081600	Enhancers	Gastric	stomach
25	chr13:76081400-76082600	Enhancers	Lung	lung
26	chr13:76081400-76083600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr13:76081600-76082200	Weak transcription	Gastric	stomach
28	chr13:76081600-76082400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
29	chr13:76081800-76082200	Enhancers	Primary B cells from peripheral blood	blood
30	chr13:76081800-76082600	Enhancers	Fetal Muscle Trunk	muscle
31	chr13:76082000-76082600	Active TSS	HepG2	liver
32	chr13:76082000-76082800	Enhancers	GM12878-XiMat	blood
33	chr13:76082200-76082600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
34	chr13:76082200-76082600	ZNF genes & repeats	Gastric	stomach
35	chr13:76082200-76086000	Weak transcription	Primary B cells from peripheral blood	blood
36	chr13:76082400-76082600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
37	chr13:76082600-76083000	Weak transcription	HepG2	liver
38	chr13:76082600-76085800	Weak transcription	Primary monocytes fromperipheralblood	blood
39	chr13:76082600-76095400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
40	chr13:76082800-76084600	Weak transcription	GM12878-XiMat	blood
41	chr13:76083000-76083200	Enhancers	HepG2	liver
42	chr13:76083200-76085800	Weak transcription	Monocytes-CD14+_RO01746	blood
43	chr13:76084600-76086200	Enhancers	GM12878-XiMat	blood
44	chr13:76085200-76086000	Enhancers	Hela-S3	cervix
45	chr13:76085400-76086200	Enhancers	Fetal Lung	lung
46	chr13:76085800-76086200	Enhancers	Monocytes-CD14+_RO01746	blood
47	chr13:76085800-76088800	Enhancers	Primary monocytes fromperipheralblood	blood
48	chr13:76086000-76087800	Enhancers	Primary B cells from peripheral blood	blood
49	chr13:76086000-76088200	Enhancers	Primary B cells from cord blood	blood
50	chr13:76086200-76086400	Flanking Active TSS	GM12878-XiMat	blood

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