Variant report

Variant	nsv430596
Chromosome Location	chr13:90467099-90659399
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1096)
CpG islands
(count:122)
Chromatin interactive
region (count:131)
LncRNA
region (count:10)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1096 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr13:90497424-90497670	K562	blood:	n/a	n/a
2	ARID3A	chr13:90551614-90552641	HepG2	liver:	n/a	n/a
3	ARID3A	chr13:90644313-90644329	K562	blood:	n/a	n/a
4	ARID3A	chr13:90520785-90520820	K562	blood:	n/a	n/a
5	ARID3A	chr13:90577420-90577637	HepG2	liver:	n/a	n/a
6	ARID3A	chr13:90512718-90512791	K562	blood:	n/a	n/a
7	ARID3A	chr13:90585018-90585218	K562	blood:	n/a	n/a
8	ARID3A	chr13:90585014-90585385	HepG2	liver:	n/a	n/a
9	ARID3A	chr13:90625281-90625544	K562	blood:	n/a	n/a
10	ATF1	chr13:90562006-90562368	K562	blood:	n/a	n/a
11	ATF1	chr13:90563357-90563940	K562	blood:	n/a	n/a
12	ATF1	chr13:90530348-90530819	K562	blood:	n/a	n/a
13	ATF1	chr13:90628499-90628699	K562	blood:	n/a	n/a
14	ATF1	chr13:90483482-90484025	K562	blood:	n/a	n/a
15	ATF1	chr13:90504797-90505152	K562	blood:	n/a	n/a
16	ATF1	chr13:90621919-90622106	K562	blood:	n/a	n/a
17	ATF1	chr13:90605296-90605645	K562	blood:	n/a	n/a
18	ATF1	chr13:90549520-90549719	K562	blood:	n/a	n/a
19	ATF1	chr13:90605873-90606073	K562	blood:	n/a	n/a
20	ATF1	chr13:90560976-90561171	K562	blood:	n/a	n/a
21	ATF1	chr13:90536949-90537223	K562	blood:	n/a	n/a
22	ATF1	chr13:90510751-90511105	K562	blood:	n/a	n/a
23	ATF1	chr13:90566492-90566927	K562	blood:	n/a	n/a
24	ATF1	chr13:90607751-90608272	K562	blood:	n/a	n/a
25	ATF1	chr13:90523739-90524152	K562	blood:	n/a	n/a
26	ATF1	chr13:90620724-90621483	K562	blood:	n/a	n/a
27	ATF1	chr13:90653192-90653460	K562	blood:	n/a	n/a
28	ATF1	chr13:90639555-90640158	K562	blood:	n/a	n/a
29	ATF1	chr13:90468064-90468577	K562	blood:	n/a	n/a
30	ATF1	chr13:90466783-90467103	K562	blood:	n/a	n/a
31	ATF1	chr13:90477390-90477952	K562	blood:	n/a	n/a
32	ATF1	chr13:90631035-90631225	K562	blood:	n/a	n/a
33	ATF1	chr13:90653786-90654041	K562	blood:	n/a	n/a
34	BACH1	chr13:90531046-90531430	K562	blood:	n/a	n/a
35	BACH1	chr13:90577633-90578315	K562	blood:	n/a	n/a
36	BACH1	chr13:90493756-90494221	K562	blood:	n/a	n/a
37	BACH1	chr13:90563752-90563952	K562	blood:	n/a	n/a
38	BACH1	chr13:90585013-90585383	H1-hESC	embryonic stem cell:	n/a	n/a
39	BACH1	chr13:90619875-90620030	K562	blood:	n/a	n/a
40	BACH1	chr13:90514969-90515132	K562	blood:	n/a	n/a
41	BACH1	chr13:90488380-90488753	K562	blood:	n/a	n/a
42	BACH1	chr13:90585829-90585878	K562	blood:	n/a	n/a
43	BACH1	chr13:90599565-90599780	K562	blood:	n/a	n/a
44	BATF	chr13:90549997-90550299	GM12878	blood:	n/a	n/a
45	BATF	chr13:90549986-90550321	GM12878	blood:	n/a	n/a
46	BHLHE40	chr13:90472685-90473042	K562	blood:	n/a	n/a
47	BHLHE40	chr13:90498120-90498598	K562	blood:	n/a	n/a
48	BHLHE40	chr13:90585012-90585389	K562	blood:	n/a	n/a
49	BHLHE40	chr13:90563800-90563984	K562	blood:	n/a	n/a
50	BHLHE40	chr13:90556476-90556676	K562	blood:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:90557520-90557570	LNCaP	prostate:	n/a
2	chr13:90536270-90536320	SK-N-SH_RA	brain:	n/a
3	chr13:90557520-90557570	HepG2	liver:	n/a
4	chr13:90557520-90557570	K562	blood:	n/a
5	chr13:90536270-90536320	CMK	blood:	n/a
6	chr13:90536270-90536320	IMR90	lung:	fetal
7	chr13:90557520-90557570	PFSK-1	brain:	n/a
8	chr13:90536270-90536320	HEK293	kidney:	embryo
9	chr13:90536270-90536320	PANC-1	pancreas:	n/a
10	chr13:90536270-90536320	NT2-D1	testis:	n/a
11	chr13:90557520-90557570	HEK293	kidney:	embryo
12	chr13:90557520-90557570	T-47D	breast:	n/a
13	chr13:90557520-90557570	GM12892	blood:	n/a
14	chr13:90536270-90536320	HRCEpiC	kidney:	n/a
15	chr13:90536270-90536320	HNPCEpiC	eye:	n/a
16	chr13:90557520-90557570	SK-N-MC	brain:	n/a
17	chr13:90536270-90536320	Hepatocyte	liver:	n/a
18	chr13:90536270-90536320	GM06990	blood:	n/a
19	chr13:90536270-90536320	MCF-7	breast:	n/a
20	chr13:90536270-90536320	SK-N-MC	brain:	n/a
21	chr13:90536270-90536320	A549	lung:	n/a
22	chr13:90557520-90557570	HRE	kidney:	n/a
23	chr13:90536270-90536320	K562	blood:	n/a
24	chr13:90536270-90536320	Hela-S3	cervix:	n/a
25	chr13:90536270-90536320	HIPEpiC	eye:	n/a
26	chr13:90536270-90536320	HCM	heart:	n/a
27	chr13:90536270-90536320	T-47D	breast:	n/a
28	chr13:90557520-90557570	AoSMC	blood vessel:	n/a
29	chr13:90536270-90536320	RPTEC	kidney:	n/a
30	chr13:90536270-90536320	ovcar-3	ovarian:	n/a
31	chr13:90557520-90557570	HAEpiC	amniotic membrane:	n/a
32	chr13:90536270-90536320	HCF	heart:	n/a
33	chr13:90536270-90536320	AG09319	gingival:	n/a
34	chr13:90557520-90557570	BJ	skin:	n/a
35	chr13:90557520-90557570	MCF-7	breast:	n/a
36	chr13:90536270-90536320	SAEC	small airway:	n/a
37	chr13:90557520-90557570	GM12878	blood:	n/a
38	chr13:90536270-90536320	NHDF-neo	bronchial:	n/a
39	chr13:90557520-90557570	Caco-2	colon:	n/a
40	chr13:90557520-90557570	SKMC	muscle:	n/a
41	chr13:90557520-90557570	RPTEC	kidney:	n/a
42	chr13:90536270-90536320	NB4	blood:	n/a
43	chr13:90536270-90536320	ProgFib	skin:	n/a
44	chr13:90536270-90536320	LNCaP	prostate:	n/a
45	chr13:90557520-90557570	AG10803	skin:	n/a
46	chr13:90536270-90536320	AG04450	lung:	fetal
47	chr13:90557520-90557570	SAEC	small airway:	n/a
48	chr13:90557520-90557570	GM06990	blood:	n/a
49	chr13:90557520-90557570	NH-A	brain:	n/a
50	chr13:90557520-90557570	HRPEpiC	eye:	n/a

(count:131 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr13:90645856..90648363-chr13:90649995..90652582,2	K562	blood:
2	chr13:90583689..90585216-chr17:41559579..41561297,2	K562	blood:
3	chr11:62607620..62610723-chr13:90583687..90586713,24	K562	blood:
4	chr13:90584688..90585192-chr3:73159622..73160587,2	MCF-7	breast:
5	chr13:90657506..90660360-chr13:90660481..90662181,2	K562	blood:
6	chr13:90613653..90615299-chr13:90617771..90620491,2	K562	blood:
7	chr13:90585208..90586708-chr5:112359217..112360718,2	K562	blood:
8	chr13:90628839..90630474-chr13:90638003..90640039,2	K562	blood:
9	chr13:90583687..90586714-chr17:41380307..41383673,9	K562	blood:
10	chr13:90503021..90505248-chr13:90522528..90525027,2	K562	blood:
11	chr13:90583687..90585197-chr9:135929982..135932962,2	K562	blood:
12	chr13:90583689..90585208-chr17:41444061..41445919,3	K562	blood:
13	chr13:90535683..90539242-chr13:90544865..90546775,3	K562	blood:
14	chr13:90512365..90514845-chr13:90515836..90518602,3	K562	blood:
15	chr10:119001200..119002700-chr13:90585187..90586694,2	MCF-7	breast:
16	chr11:62609120..62610720-chr13:90583687..90586690,7	MCF-7	breast:
17	chr13:90628839..90630474-chr13:90638003..90640039,2	K562	blood:
18	chr13:90585210..90586713-chr17:41438934..41440457,2	MCF-7	breast:
19	chr13:90615424..90617476-chr13:90620139..90623091,2	K562	blood:
20	chr13:90494528..90497292-chr13:90501979..90504191,2	K562	blood:
21	chr13:90593285..90595272-chr13:90597224..90598967,2	K562	blood:
22	chr11:62607620..62610723-chr13:90583688..90586715,22	K562	blood:
23	chr11:62609126..62609718-chr13:90584688..90585208,7	MCF-7	breast:
24	chr13:90593285..90595272-chr13:90597224..90598967,2	K562	blood:
25	chr13:90596974..90598831-chr13:90602798..90605070,2	K562	blood:
26	chr13:90590871..90593494-chr13:90596073..90598011,2	K562	blood:
27	chr13:90471832..90475214-chr13:90475498..90478937,3	K562	blood:
28	chr13:90497383..90499732-chr13:90531093..90533343,2	K562	blood:
29	chr13:90576825..90578329-chr13:90580661..90582682,2	K562	blood:
30	chr13:90584688..90585211-chr3:73159599..73160120,2	Hela-S3	cervix:
31	chr13:90585195..90585712-chr17:41465633..41466487,2	HCT-116	colon:
32	chr13:90497518..90499702-chr13:90509556..90511719,2	K562	blood:
33	chr13:90451472..90453159-chr13:90467765..90470147,2	K562	blood:
34	chr11:10961117..10964097-chr13:90585214..90586717,2	K562	blood:
35	chr11:62609117..62609700-chr13:90584687..90585217,12	HCT-116	colon:
36	chr13:90583688..90585209-chr6:29527999..29529519,2	K562	blood:
37	chr13:90590871..90593494-chr13:90596073..90598011,2	K562	blood:
38	chr13:90615424..90617476-chr13:90620139..90623091,2	K562	blood:
39	chr13:90494528..90497292-chr13:90501979..90504191,2	K562	blood:
40	chr13:90513066..90514981-chr13:90520544..90522949,2	K562	blood:
41	chr11:62608617..62609723-chr13:90584689..90585209,9	Hela-S3	cervix:
42	chr13:90512365..90514845-chr13:90515836..90518602,3	K562	blood:
43	chr13:90567117..90569538-chr13:90570624..90572320,2	K562	blood:
44	chr13:90584707..90585217-chr9:71420682..71421182,2	HCT-116	colon:
45	chr13:90585193..90585714-chr17:41465692..41466303,3	MCF-7	breast:
46	chr13:90584687..90585215-chr16:19462956..19463476,2	HCT-116	colon:
47	chr13:90585187..90586690-chr17:41391871..41393483,2	K562	blood:
48	chr13:90497518..90499702-chr13:90509556..90511719,2	K562	blood:
49	chr13:90583687..90586713-chr17:41380286..41383689,12	K562	blood:
50	chr10:103124608..103126131-chr13:90583695..90586710,5	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SLITRK6-28	chr13:90580934-90581047	NONHSAT034639
2	lnc-SLITRK6-28	chr13:90581478-90581583	l_900_chr13:90577875-90581583_kidney
3	lnc-SLITRK6-28	chr13:90577868-90578113	NONHSAT034638
4	lnc-SLITRK6-28	chr13:90580934-90581047	l_900_chr13:90577875-90581583_kidney
5	lnc-SLITRK6-27	chr13:90537509-90537789	NONHSAT034637
6	lnc-SLITRK6-27	chr13:90539777-90539848	NONHSAT034637
7	lnc-SLITRK6-28	chr13:90581478-90581662	NONHSAT034638
8	lnc-SLITRK6-28	chr13:90577907-90578113	NONHSAT034639
9	lnc-SLITRK6-28	chr13:90581478-90581620	NONHSAT034639
10	lnc-SLITRK6-28	chr13:90577876-90578113	l_900_chr13:90577875-90581583_kidney

No data

Variant related genes	Relation type
RPL7L1P1	TF binding region
ENSG00000200733	TF binding region
PEX12P1	TF binding region
RPL7L1P1	CpG island
ENSG00000200733	CpG island
PEX12P1	CpG island
ENSG00000236383	chromatin interactions
ENSG00000215417	chromatin interactions
ENSG00000130304	chromatin interactions
ENSG00000225936	chromatin interactions
ENSG00000234227	chromatin interactions
ENSG00000188825	chromatin interactions
ENSG00000148308	chromatin interactions
ENSG00000110700	chromatin interactions
ENSG00000222414	chromatin interactions
ENSG00000236905	chromatin interactions
ENSG00000067596	chromatin interactions
ENSG00000223247	chromatin interactions
ENSG00000133316	chromatin interactions
ENSG00000200733	chromatin interactions

Extended variants
information (count: 2765 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:2765 , 50 per page) page: 1 2 3 4 5 6 7 ... 56

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9522748	chr13:90468215-90468216	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs567115678	chr13:90468229-90468230	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs534618421	chr13:90468298-90468299	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs117777728	chr13:90468319-90468320	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs571417859	chr13:90468375-90468376	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs191531895	chr13:90468420-90468421	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs182290416	chr13:90468462-90468463	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs576788339	chr13:90468472-90468473	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs543730260	chr13:90468481-90468482	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs146378303	chr13:90468518-90468519	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs189228954	chr13:90468534-90468535	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs577271141	chr13:90468540-90468541	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs559410692	chr13:90468565-90468566	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs193111291	chr13:90468572-90468573	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs544781275	chr13:90468576-90468577	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs563113688	chr13:90468600-90468601	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs540211903	chr13:90474614-90474615	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs564847183	chr13:90474616-90474617	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs371543475	chr13:90474650-90474651	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs140481420	chr13:90474655-90474656	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs531123592	chr13:90474676-90474677	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs75330726	chr13:90474769-90474770	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs7987826	chr13:90474781-90474782	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs558627943	chr13:90474819-90474820	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs559572432	chr13:90474827-90474828	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs546902726	chr13:90474841-90474842	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs571574007	chr13:90474851-90474852	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs538656955	chr13:90474864-90474865	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs557425979	chr13:90474871-90474872	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs569295729	chr13:90474884-90474885	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs201848651	chr13:90474896-90474897	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs536433644	chr13:90474897-90474898	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs9583738	chr13:90474912-90474913	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs573096683	chr13:90474914-90474915	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs115896631	chr13:90474930-90474931	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs558902018	chr13:90474945-90474946	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs9588767	chr13:90474952-90474953	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs556767378	chr13:90474992-90474993	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs543909596	chr13:90475001-90475002	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs576681886	chr13:90475026-90475027	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs9560453	chr13:90475036-90475037	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs574475784	chr13:90475095-90475096	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs541543956	chr13:90475096-90475097	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs554273668	chr13:90475157-90475158	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs561108740	chr13:90475315-90475316	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs528668788	chr13:90475366-90475367	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs546841507	chr13:90475392-90475393	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs565488809	chr13:90475399-90475400	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs370037797	chr13:90475411-90475412	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs117254836	chr13:90475434-90475435	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:90)

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
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
Myoepithelioma	18604193	CNVD
Breast cancer	17133270	CNVD
Prostate cancer	18632612	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Melanoma	18172304	CNVD
Prostate cancer	16573809	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Basal cell lymphoma	17053054	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Metanephric adenoma	20802469	CNVD
Gastric cancer	17908304	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Liposarcoma	21253554	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
abnormal development	18461090	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal cancer	21851588	CNVD
Prostate cancer	21965145	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Cancer	21220470	CNVD
Cancer	21183584	CNVD
Omodysplasia	19481194	CNVD
Breast cancer	22032731	CNVD
Mantle cell lymphoma	19690137	CNVD
Rhabdomyosarcoma	17210683	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Breast cancer	21364760	CNVD
Medulloblastoma	19270706	CNVD
Myelofibrosis	22110671	CNVD
coloboma	21285886	CNVD
Cancer	20164920	CNVD
Burkitt''s lymphoma	19759907	CNVD
Wilms tumour	21544195	CNVD
Acute myeloid leukemia	19651601	CNVD
Effusion lymphoma	18079361	CNVD
Developmental delay	21147756	CNVD
Burkitt''s lymphoma	20823134	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:149 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:90468200-90468600	Enhancers	Cortex derived primary cultured neurospheres	brain
2	chr13:90474600-90475000	Enhancers	Brain Cingulate Gyrus	brain
3	chr13:90474600-90475200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr13:90474800-90475000	Enhancers	A549	lung
5	chr13:90475000-90479800	Weak transcription	Brain Cingulate Gyrus	brain
6	chr13:90475200-90479800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr13:90479400-90480000	Enhancers	Brain Angular Gyrus	brain
8	chr13:90479400-90480400	Enhancers	Brain Inferior Temporal Lobe	brain
9	chr13:90479800-90480000	Active TSS	Brain Anterior Caudate	brain
10	chr13:90479800-90480200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr13:90479800-90480200	Enhancers	Brain Cingulate Gyrus	brain
12	chr13:90479800-90480200	Enhancers	Brain Hippocampus Middle	brain
13	chr13:90479800-90480400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr13:90479800-90480400	Enhancers	Brain Substantia Nigra	brain
15	chr13:90479800-90481600	Enhancers	Adipose Nuclei	Adipose
16	chr13:90480000-90480200	Flanking Active TSS	Brain Angular Gyrus	brain
17	chr13:90480000-90480200	Flanking Active TSS	Brain Anterior Caudate	brain
18	chr13:90480000-90480400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr13:90480000-90480400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
20	chr13:90480000-90480400	Enhancers	Fetal Lung	lung
21	chr13:90480200-90484600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
22	chr13:90480400-90482600	Weak transcription	Fetal Lung	lung
23	chr13:90480400-90484600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr13:90482600-90483200	Enhancers	Fetal Lung	lung
25	chr13:90483200-90485200	Weak transcription	Fetal Lung	lung
26	chr13:90483800-90484000	Enhancers	A549	lung
27	chr13:90484000-90485000	Weak transcription	A549	lung
28	chr13:90484600-90485200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
29	chr13:90484600-90485400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr13:90485000-90485400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr13:90485000-90486000	Enhancers	A549	lung
32	chr13:90485200-90485600	Enhancers	H9 Cell Line	embryonic stem cell
33	chr13:90485200-90485800	Enhancers	Fetal Lung	lung
34	chr13:90492000-90492400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr13:90492000-90492400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
36	chr13:90498200-90500000	Enhancers	Fetal Lung	lung
37	chr13:90499200-90500000	Enhancers	Muscle Satellite Cultured Cells	--
38	chr13:90508600-90509000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr13:90514600-90515400	Enhancers	HMEC	breast
40	chr13:90515000-90515400	Enhancers	HUVEC	blood vessel
41	chr13:90515400-90516400	Weak transcription	HUVEC	blood vessel
42	chr13:90516400-90518200	Enhancers	HUVEC	blood vessel
43	chr13:90536000-90536400	Active TSS	Cortex derived primary cultured neurospheres	brain
44	chr13:90543400-90544200	Enhancers	HUVEC	blood vessel
45	chr13:90550400-90551800	Enhancers	HepG2	liver
46	chr13:90551800-90552000	Flanking Active TSS	HepG2	liver
47	chr13:90552000-90552400	Enhancers	HepG2	liver
48	chr13:90552200-90552600	Enhancers	Rectal Mucosa Donor 31	rectum
49	chr13:90552200-90552800	Enhancers	HUVEC	blood vessel
50	chr13:90552400-90552600	Enhancers	Muscle Satellite Cultured Cells	--

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