Variant report

Variant	esv3510680
Chromosome Location	chr13:48236624-48498185
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1558)
CpG islands
(count:306)
Chromatin interactive
region (count:21)
LncRNA
region (count:23)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1558 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr13:48432383-48432990	HepG2	liver:	n/a	n/a
2	ATF3	chr13:48270741-48271071	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr13:48348255-48348467	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr13:48403886-48404138	K562	blood:	n/a	n/a
5	BATF	chr13:48417111-48417380	GM12878	blood:	n/a	n/a
6	BCL11A	chr13:48390923-48391228	H1-hESC	embryonic stem cell:	n/a	chr13:48391167-48391174
7	BDP1	chr13:48348031-48348362	Hela-S3	cervix:	n/a	n/a
8	BHLHE40	chr13:48443796-48444273	GM12878	blood:	n/a	n/a
9	BHLHE40	chr13:48432486-48432688	HepG2	liver:	n/a	n/a
10	BHLHE40	chr13:48417321-48417465	GM12878	blood:	n/a	n/a
11	BRCA1	chr13:48373395-48373404	GM12878	blood:	n/a	n/a
12	BRCA1	chr13:48250058-48250195	Hela-S3	cervix:	n/a	n/a
13	BRCA1	chr13:48246836-48248088	Hela-S3	cervix:	n/a	n/a
14	BRCA1	chr13:48348211-48348608	Hela-S3	cervix:	n/a	n/a
15	BRCA1	chr13:48282473-48283163	Hela-S3	cervix:	n/a	n/a
16	BRCA1	chr13:48300329-48300945	Hela-S3	cervix:	n/a	n/a
17	CBX3	chr13:48478334-48478745	K562	blood:	n/a	n/a
18	CEBPB	chr13:48336343-48336678	IMR90	lung:	n/a	chr13:48336502-48336513
19	CEBPB	chr13:48477968-48478327	IMR90	lung:	n/a	n/a
20	CEBPB	chr13:48246653-48248107	Hela-S3	cervix:	n/a	chr13:48247040-48247051
21	CEBPB	chr13:48246903-48247596	IMR90	lung:	n/a	chr13:48247040-48247051
22	CEBPB	chr13:48470738-48471049	HepG2	liver:	n/a	n/a
23	CEBPB	chr13:48432390-48432769	HepG2	liver:	n/a	n/a
24	CEBPB	chr13:48254928-48255198	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr13:48405420-48405756	HepG2	liver:	n/a	chr13:48405585-48405596
26	CEBPB	chr13:48325433-48325531	H1-hESC	embryonic stem cell:	n/a	n/a
27	CEBPB	chr13:48464349-48464658	Hela-S3	cervix:	n/a	n/a
28	CEBPB	chr13:48247239-48247399	A549	lung:	n/a	n/a
29	CEBPB	chr13:48477973-48478318	Hela-S3	cervix:	n/a	n/a
30	CEBPB	chr13:48347713-48347889	H1-hESC	embryonic stem cell:	n/a	n/a
31	CEBPB	chr13:48336347-48336671	HepG2	liver:	n/a	chr13:48336502-48336513
32	CEBPB	chr13:48364782-48365014	HepG2	liver:	n/a	chr13:48364903-48364914
33	CEBPB	chr13:48250192-48250392	Hela-S3	cervix:	n/a	n/a
34	CEBPB	chr13:48354409-48354426	A549	lung:	n/a	chr13:48354409-48354422
35	CEBPB	chr13:48282642-48283001	MCF-7	breast:	n/a	n/a
36	CEBPB	chr13:48347765-48348625	Hela-S3	cervix:	n/a	n/a
37	CEBPB	chr13:48253395-48253933	Hela-S3	cervix:	n/a	n/a
38	CEBPB	chr13:48354463-48354553	K562	blood:	n/a	n/a
39	CEBPB	chr13:48439669-48439786	HepG2	liver:	n/a	chr13:48439760-48439771 chr13:48439758-48439769 chr13:48439760-48439771
40	CEBPB	chr13:48439601-48439930	HepG2	liver:	n/a	chr13:48439760-48439771 chr13:48439758-48439769 chr13:48439760-48439771
41	CEBPB	chr13:48364838-48364977	K562	blood:	n/a	chr13:48364903-48364914
42	CEBPB	chr13:48405490-48405702	Hela-S3	cervix:	n/a	chr13:48405585-48405596
43	CEBPB	chr13:48354240-48354719	HepG2	liver:	n/a	chr13:48354409-48354422
44	CEBPB	chr13:48263336-48263392	IMR90	lung:	n/a	chr13:48263357-48263370
45	CEBPB	chr13:48325369-48325631	IMR90	lung:	n/a	n/a
46	CEBPB	chr13:48269895-48270168	HepG2	liver:	n/a	chr13:48270007-48270018
47	CEBPB	chr13:48364802-48364996	IMR90	lung:	n/a	chr13:48364903-48364914
48	CEBPB	chr13:48336454-48336647	Hela-S3	cervix:	n/a	chr13:48336502-48336513
49	CEBPB	chr13:48364855-48364927	Hela-S3	cervix:	n/a	chr13:48364903-48364914
50	CEBPB	chr13:48354349-48354614	IMR90	lung:	n/a	chr13:48354409-48354422

(count:306 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:48478591-48478641	ProgFib	skin:	n/a
2	chr13:48478591-48478641	ProgFib	skin:	n/a
3	chr13:48388426-48388476	HRCEpiC	kidney:	n/a
4	chr13:48478546-48478596	BE2_C	brain:	n/a
5	chr13:48391043-48391093	NT2-D1	testis:	n/a
6	chr13:48412113-48412163	HCF	heart:	n/a
7	chr13:48478591-48478641	MCF-7	breast:	n/a
8	chr13:48478591-48478641	HRE	kidney:	n/a
9	chr13:48478591-48478641	HPAEpiC	pulmonary alveolar:	n/a
10	chr13:48412113-48412163	BJ	skin:	n/a
11	chr13:48388426-48388476	HL-60	blood:	n/a
12	chr13:48478546-48478596	HMEC	breast:	n/a
13	chr13:48388426-48388476	NB4	blood:	n/a
14	chr13:48478591-48478641	GM06990	blood:	n/a
15	chr13:48412113-48412163	BE2_C	brain:	n/a
16	chr13:48388426-48388476	GM19239	blood:	n/a
17	chr13:48478591-48478641	PANC-1	pancreas:	n/a
18	chr13:48391043-48391093	CMK	blood:	n/a
19	chr13:48478546-48478596	MCF-7	breast:	n/a
20	chr13:48388426-48388476	HEEpiC	esophagus:	n/a
21	chr13:48391043-48391093	U87	brain:	n/a
22	chr13:48412113-48412163	PANC-1	pancreas:	n/a
23	chr13:48478591-48478641	SK-N-MC	brain:	n/a
24	chr13:48478591-48478641	AG10803	skin:	n/a
25	chr13:48412113-48412163	IMR90	lung:	fetal
26	chr13:48478591-48478641	HEEpiC	esophagus:	n/a
27	chr13:48388426-48388476	NH-A	brain:	n/a
28	chr13:48478591-48478641	HL-60	blood:	n/a
29	chr13:48478546-48478596	Hela-S3	cervix:	n/a
30	chr13:48391043-48391093	GM06990	blood:	n/a
31	chr13:48388426-48388476	SAEC	small airway:	n/a
32	chr13:48478591-48478641	AG04450	lung:	fetal
33	chr13:48391043-48391093	AG04450	lung:	fetal
34	chr13:48412113-48412163	HCT-116	colon:	n/a
35	chr13:48478546-48478596	HUVEC	blood vessel:	n/a
36	chr13:48412113-48412163	HRPEpiC	eye:	n/a
37	chr13:48388426-48388476	SKMC	muscle:	n/a
38	chr13:48388426-48388476	GM06990	blood:	n/a
39	chr13:48412113-48412163	A549	lung:	n/a
40	chr13:48478591-48478641	H1-hESC	embryonic stem cell:	embryo
41	chr13:48391043-48391093	BE2_C	brain:	n/a
42	chr13:48391043-48391093	PANC-1	pancreas:	n/a
43	chr13:48478546-48478596	NH-A	brain:	n/a
44	chr13:48478546-48478596	CMK	blood:	n/a
45	chr13:48412113-48412163	PFSK-1	brain:	n/a
46	chr13:48412113-48412163	NHDF-neo	bronchial:	n/a
47	chr13:48478546-48478596	HCT-116	colon:	n/a
48	chr13:48391043-48391093	NHBE	bronchial:	n/a
49	chr13:48412113-48412163	SKMC	muscle:	n/a
50	chr13:48412113-48412163	HIPEpiC	eye:	n/a

(count:21 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr13:48371410..48374198-chr13:48468261..48469829,2	MCF-7	breast:
2	chr13:48373223..48373750-chr13:48512933..48513507,2	MCF-7	breast:
3	chr13:48380767..48383194-chr13:48392784..48395311,2	MCF-7	breast:
4	chr13:48466792..48469518-chr13:48521553..48523936,2	MCF-7	breast:
5	chr13:48480107..48482697-chr13:48488766..48491546,2	K562	blood:
6	chr13:48371410..48374198-chr13:48468261..48469829,2	MCF-7	breast:
7	chr13:48373048..48373868-chr13:48611844..48612676,2	MCF-7	breast:
8	chr13:48404817..48407673-chr13:48410344..48411891,2	K562	blood:
9	chr13:48373135..48373727-chr13:48561238..48561832,3	MCF-7	breast:
10	chr13:48449894..48450717-chr7:134300210..134301125,2	MCF-7	breast:
11	chr13:48372840..48373623-chr13:48512914..48513683,3	MCF-7	breast:
12	chr13:48404817..48407673-chr13:48410344..48411891,2	K562	blood:
13	chr13:48380767..48383194-chr13:48392784..48395311,2	MCF-7	breast:
14	chr13:48440591..48443452-chr13:48454032..48455862,2	MCF-7	breast:
15	chr13:48400233..48402500-chr13:48467712..48470091,2	MCF-7	breast:
16	chr13:48440591..48443452-chr13:48454032..48455862,2	MCF-7	breast:
17	chr13:48470064..48472473-chr13:48479999..48482410,2	MCF-7	breast:
18	chr11:70414027..70414931-chr13:48252954..48253516,2	MCF-7	breast:
19	chr13:48338058..48339804-chr13:48349149..48350961,2	K562	blood:
20	chr13:48400233..48402500-chr13:48467712..48470091,2	MCF-7	breast:
21	chr13:48338058..48339804-chr13:48349149..48350961,2	K562	blood:

(count:23 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SUCLA2-3	chr13:48443896-48444401	NONHSAT033689
2	lnc-SUCLA2-4	chr13:48464985-48466403	XLOC_010601
3	lnc-SUCLA2-5	chr13:48399465-48399562	ENSG00000228573
4	lnc-NUDT15-4	chr13:48477761-48477842	NONHSAT033691
5	lnc-SUCLA2-6	chr13:48278996-48279452	XLOC_010599
6	lnc-SUCLA2-3	chr13:48481466-48481492	ENSG00000234689
7	lnc-NUDT15-4	chr13:48478857-48479040	NONHSAT033691
8	lnc-SUCLA2-4	chr13:48466673-48466696	XLOC_010601
9	lnc-NUDT15-5	chr13:48337790-48337868	NONHSAT033686
10	lnc-SUCLA2-6	chr13:48273752-48273914	XLOC_010599
11	lnc-SUCLA2-3	chr13:48481153-48481270	ENSG00000234689
12	lnc-SUCLA2-3	chr13:48444416-48444464	NONHSAT033689
13	lnc-SUCLA2-3	chr13:48399476-48399520	NONHSAT033689
14	lnc-SUCLA2-3	chr13:48400274-48400425	NONHSAT033689
15	lnc-NUDT15-5	chr13:48337878-48337963	NONHSAT033686
16	lnc-SUCLA2-3	chr13:48481153-48481270	NONHSAT033689
17	lnc-SUCLA2-7	chr13:48340775-48341220	NONHSAT033687
18	lnc-SUCLA2-6	chr13:48270851-48270892	XLOC_010599
19	lnc-SUCLA2-3	chr13:48479464-48479533	ENSG00000234689
20	lnc-SUCLA2-5	chr13:48409931-48410091	ENSG00000228573
21	lnc-NUDT15-5	chr13:48337520-48337603	NONHSAT033686
22	lnc-SUCLA2-8	chr13:48321381-48321699	NONHSAT033685
23	lnc-SUCLA2-5	chr13:48400274-48400425	ENSG00000228573

No data

Variant related genes	Relation type
NAP1L4P3	TF binding region
ENSG00000228573	TF binding region
RPL27AP8	TF binding region
LINC00444	TF binding region
NAP1L4P3	CpG island
ENSG00000228573	CpG island
RPL27AP8	CpG island
LINC00444	CpG island
ENSG00000136143	chromatin interactions
ENSG00000234689	chromatin interactions
OSBPL9	miRNA target sites

Extended variants
information (count: 6188 )
Associated
traits (count: 125 )

Variant overlapped rSNPs/rCNVs (count:6188 , 50 per page) page: 1 2 3 4 5 6 7 ... 124

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs535572896	chr13:48236645-48236646	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs562574367	chr13:48236748-48236749	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs377751834	chr13:48236757-48236758	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs577691664	chr13:48236783-48236784	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs545206458	chr13:48236802-48236803	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs560437452	chr13:48236819-48236820	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs527487189	chr13:48236824-48236825	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs549258625	chr13:48236845-48236846	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs550863085	chr13:48236909-48236910	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs114479303	chr13:48236927-48236928	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs529262148	chr13:48236946-48236947	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs113170663	chr13:48236956-48236957	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs571147228	chr13:48236975-48236976	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs145068202	chr13:48237018-48237019	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs551554153	chr13:48237025-48237026	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs79006632	chr13:48237026-48237027	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs534131756	chr13:48237089-48237090	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs555606557	chr13:48237118-48237119	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs574273116	chr13:48237141-48237142	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs187132799	chr13:48237159-48237160	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs9634809	chr13:48237161-48237162	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs191561584	chr13:48237197-48237198	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs183283522	chr13:48237200-48237201	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs545079526	chr13:48237201-48237202	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs560300495	chr13:48237225-48237226	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs113770100	chr13:48237230-48237231	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs58152499	chr13:48237289-48237290	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs561216940	chr13:48237304-48237305	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs1172410	chr13:48237322-48237323	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs560848883	chr13:48237343-48237344	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs566744691	chr13:48237361-48237362	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs59064381	chr13:48237395-48237396	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs2677601	chr13:48237402-48237403	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs138501512	chr13:48237422-48237423	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs533362477	chr13:48237423-48237424	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs75892467	chr13:48237428-48237429	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs61097923	chr13:48237429-48237430	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs12863535	chr13:48237430-48237431	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs1748597	chr13:48237451-48237452	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs398022649	chr13:48237452-48237453	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs28559615	chr13:48237453-48237454	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs551418189	chr13:48237481-48237482	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs1926485	chr13:48237507-48237508	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs367984442	chr13:48237540-48237541	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs534099017	chr13:48237636-48237637	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs549193477	chr13:48237640-48237641	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs111329261	chr13:48237641-48237642	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs372984647	chr13:48237642-48237643	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs567931931	chr13:48237671-48237672	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs543656107	chr13:48237672-48237673	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:125)

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
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Squamous cell cancer	20885788	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Thyroid cancer	19087340	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Ovarian cancer	22174824	CNVD
Breast cancer	17899364	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Colorectal cancer	16774939	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17133270	CNVD
Myoepithelioma	18604193	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Trisomy	24170809	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Alveolar rhabdomyosarcoma	16790082	CNVD
Prostate cancer	16573809	CNVD
Prostate cancer	18632612	CNVD
Paraganglioma	21461997	CNVD
Pheochromocytoma	21461997	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Prostate cancer	19242612	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	17245344	CNVD
Colorectal cancer	21586687	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Retinoblastoma	19183342	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Developmental delay	21147756	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Melanoma	18172304	CNVD
Retinoblastoma	21504564	CNVD
Chronic lymphocytic leukemia	21795749	CNVD
Chronic lymphocytic leukemia	17805327	CNVD
Mental retardation	17502991	CNVD
Retinoblastoma	17502991	CNVD
Bipolar disorder	18458673	CNVD
Liposarcoma	21253554	CNVD
T-cell lymphomas	19863542	CNVD
Cervical cancer	21062161	CNVD
microdeletion syndrome	19284877	CNVD
Ovarian cancer	22355333	CNVD
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	17053054	CNVD
Multiple myeloma	19135901	CNVD
Autism	18414403	CNVD
Neurocytoma	17123091	CNVD
Central neurocytomas	17123091	CNVD
Prostate cancer	16461572	CNVD
Merkel cell carcinoma	19020549	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
lymphocytic leukemia	21291569	CNVD
Multiple myeloma	17550852	CNVD
Myelofibrosis	22110671	CNVD
Prostate cancer	21088497	CNVD
Colorectal cancer	21645411	CNVD
Breast cancer	22048815	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Glioblastoma multiforme	21750150	CNVD
Chronic lymphocytic leukemia	21049055	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Non-small cell lung cancer	21829676	CNVD
Phyllodes tumor	17334353	CNVD
Retinoblastoma	22278416	CNVD
Glioblastoma multiforme	19435819	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Breast cancer	21858162	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Acute myeloid leukemia	21251322	CNVD
Acute myeloid leukemia	20729466	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Lung adenocarcinoma	21935476	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Pancreatic cancer	17952125	CNVD

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:48236200-48239000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
2	chr13:48236200-48239400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
3	chr13:48238400-48239400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr13:48238400-48239400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr13:48238600-48239200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr13:48238600-48239200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
7	chr13:48238600-48239400	Enhancers	H1 Cell Line	embryonic stem cell
8	chr13:48238600-48239400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr13:48238600-48239400	Enhancers	iPS-20b Cell Line	embryonic stem cell
10	chr13:48238800-48239400	Enhancers	HUES64 Cell Line	embryonic stem cell
11	chr13:48238800-48239400	Enhancers	iPS-15b Cell Line	embryonic stem cell
12	chr13:48238800-48239400	Enhancers	iPS-18 Cell Line	embryonic stem cell
13	chr13:48239000-48239400	Enhancers	ES-I3 Cell Line	embryonic stem cell
14	chr13:48239000-48239400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr13:48239000-48239600	Enhancers	HUES48 Cell Line	embryonic stem cell
16	chr13:48245400-48245800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
17	chr13:48245400-48245800	Enhancers	NHDF-Ad	bronchial
18	chr13:48245400-48246400	Enhancers	Skeletal Muscle Male	skeletal muscle
19	chr13:48245400-48248000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
20	chr13:48245600-48246000	Enhancers	Fetal Brain Male	brain
21	chr13:48245600-48249600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
22	chr13:48245800-48246000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr13:48245800-48246000	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
24	chr13:48245800-48246200	Flanking Active TSS	NHDF-Ad	bronchial
25	chr13:48245800-48248000	Enhancers	Skeletal Muscle Female	skeletal muscle
26	chr13:48245800-48248400	Enhancers	Hela-S3	cervix
27	chr13:48246000-48246200	Weak transcription	Fetal Brain Male	brain
28	chr13:48246000-48246400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr13:48246000-48246400	Enhancers	NHLF	lung
30	chr13:48246000-48246800	Enhancers	Fetal Stomach	stomach
31	chr13:48246000-48247200	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr13:48246000-48247800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
33	chr13:48246000-48248000	Enhancers	HSMMtube	muscle
34	chr13:48246200-48246400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
35	chr13:48246200-48246600	Enhancers	Fetal Brain Male	brain
36	chr13:48246200-48248000	Enhancers	NHDF-Ad	bronchial
37	chr13:48246400-48246600	Enhancers	Psoas Muscle	Psoas
38	chr13:48246400-48246800	Enhancers	Fetal Lung	lung
39	chr13:48246400-48246800	Enhancers	Fetal Muscle Leg	muscle
40	chr13:48246400-48246800	Enhancers	Right Atrium	heart
41	chr13:48246400-48246800	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
42	chr13:48246400-48247200	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
43	chr13:48246400-48247400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
44	chr13:48246400-48247600	Weak transcription	NHLF	lung
45	chr13:48246400-48247800	Enhancers	Adipose Nuclei	Adipose
46	chr13:48246400-48248000	Enhancers	Muscle Satellite Cultured Cells	--
47	chr13:48246400-48248000	Enhancers	NH-A	brain
48	chr13:48246600-48247200	Weak transcription	Psoas Muscle	Psoas
49	chr13:48246600-48247400	Weak transcription	Fetal Brain Male	brain
50	chr13:48246800-48247200	Weak transcription	Fetal Lung	lung

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