Variant report

Variant	nsv563123
Chromosome Location	chr13:111237260-111292044
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1645)
CpG islands
(count:3484)
Chromatin interactive
region (count:90)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1645 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr13:111245912-111246135	K562	blood:	n/a	n/a
2	ARID3A	chr13:111246487-111246644	K562	blood:	n/a	n/a
3	ARID3A	chr13:111245908-111246118	HepG2	liver:	n/a	n/a
4	ARID3A	chr13:111270041-111270363	K562	blood:	n/a	n/a
5	ARID3A	chr13:111267627-111268132	HepG2	liver:	n/a	n/a
6	ARID3A	chr13:111267685-111267885	K562	blood:	n/a	n/a
7	ARID3A	chr13:111242353-111242710	HepG2	liver:	n/a	n/a
8	ATF2	chr13:111263291-111264210	GM12878	blood:	n/a	n/a
9	ATF2	chr13:111269691-111269959	H1-hESC	embryonic stem cell:	n/a	chr13:111269830-111269841
10	ATF2	chr13:111268498-111269019	GM12878	blood:	n/a	n/a
11	ATF2	chr13:111291711-111291958	GM12878	blood:	n/a	n/a
12	ATF2	chr13:111269617-111270029	H1-hESC	embryonic stem cell:	n/a	chr13:111269830-111269841
13	ATF2	chr13:111263279-111264374	GM12878	blood:	n/a	n/a
14	ATF2	chr13:111267649-111268098	GM12878	blood:	n/a	n/a
15	BACH1	chr13:111267862-111268018	H1-hESC	embryonic stem cell:	n/a	n/a
16	BACH1	chr13:111249719-111250046	K562	blood:	n/a	n/a
17	BACH1	chr13:111262346-111262547	K562	blood:	n/a	n/a
18	BACH1	chr13:111243055-111243185	H1-hESC	embryonic stem cell:	n/a	n/a
19	BATF	chr13:111260051-111260403	GM12878	blood:	n/a	n/a
20	BATF	chr13:111268661-111268970	GM12878	blood:	n/a	chr13:111268810-111268821 chr13:111268811-111268821
21	BATF	chr13:111263251-111264016	GM12878	blood:	n/a	n/a
22	BATF	chr13:111263512-111263938	GM12878	blood:	n/a	n/a
23	BATF	chr13:111268630-111269012	GM12878	blood:	n/a	chr13:111268810-111268821 chr13:111268811-111268821
24	BATF	chr13:111260075-111260366	GM12878	blood:	n/a	n/a
25	BCL11A	chr13:111263261-111263935	GM12878	blood:	n/a	n/a
26	BCL11A	chr13:111263531-111263876	GM12878	blood:	n/a	n/a
27	BCL11A	chr13:111268566-111268980	GM12878	blood:	n/a	n/a
28	BCL11A	chr13:111263323-111263515	GM12878	blood:	n/a	n/a
29	BCL3	chr13:111288436-111289023	GM12878	blood:	n/a	n/a
30	BCL3	chr13:111288430-111289017	GM12878	blood:	n/a	n/a
31	BCL3	chr13:111277242-111277728	GM12878	blood:	n/a	n/a
32	BCL3	chr13:111290622-111290977	GM12878	blood:	n/a	n/a
33	BCL3	chr13:111277242-111277713	GM12878	blood:	n/a	n/a
34	BCLAF1	chr13:111268478-111268914	GM12878	blood:	n/a	n/a
35	BCLAF1	chr13:111263193-111264009	GM12878	blood:	n/a	n/a
36	BCLAF1	chr13:111267636-111268153	GM12878	blood:	n/a	n/a
37	BHLHE40	chr13:111268565-111268616	K562	blood:	n/a	n/a
38	BHLHE40	chr13:111268661-111269317	GM12878	blood:	n/a	n/a
39	BHLHE40	chr13:111267534-111268165	HepG2	liver:	n/a	n/a
40	BHLHE40	chr13:111267509-111268025	GM12878	blood:	n/a	n/a
41	BHLHE40	chr13:111267508-111267920	K562	blood:	n/a	n/a
42	BHLHE40	chr13:111245960-111246088	K562	blood:	n/a	n/a
43	BHLHE40	chr13:111263349-111263865	GM12878	blood:	n/a	n/a
44	BHLHE40	chr13:111254556-111254892	K562	blood:	n/a	n/a
45	BRCA1	chr13:111245860-111246205	Hela-S3	cervix:	n/a	n/a
46	BRCA1	chr13:111267579-111268094	Hela-S3	cervix:	n/a	n/a
47	BRCA1	chr13:111262345-111262546	HepG2	liver:	n/a	n/a
48	BRCA1	chr13:111268844-111268989	HepG2	liver:	n/a	n/a
49	BRCA1	chr13:111267608-111268353	HepG2	liver:	n/a	n/a
50	CBX3	chr13:111254487-111254819	K562	blood:	n/a	n/a

(count:3484 , 50 per page) page: 1 2 3 4 5 6 7 ... 70

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:111267667-111267717	NT2-D1	testis:	n/a
2	chr13:111286999-111287049	Hepatocyte	liver:	n/a
3	chr13:111268031-111268081	HRE	kidney:	n/a
4	chr13:111291955-111292005	MCF-7	breast:	n/a
5	chr13:111278058-111278108	Hepatocyte	liver:	n/a
6	chr13:111291316-111291366	HCF	heart:	n/a
7	chr13:111291685-111291735	PFSK-1	brain:	n/a
8	chr13:111267667-111267717	NT2-D1	testis:	n/a
9	chr13:111286999-111287049	Hepatocyte	liver:	n/a
10	chr13:111268031-111268081	HRE	kidney:	n/a
11	chr13:111291955-111292005	MCF-7	breast:	n/a
12	chr13:111278058-111278108	Hepatocyte	liver:	n/a
13	chr13:111291316-111291366	HCF	heart:	n/a
14	chr13:111291685-111291735	PFSK-1	brain:	n/a
15	chr13:111287944-111287994	PrEC	prostate:	n/a
16	chr13:111285565-111285615	HUVEC	blood vessel:	n/a
17	chr13:111285565-111285615	Caco-2	colon:	n/a
18	chr13:111290755-111290805	SAEC	small airway:	n/a
19	chr13:111268017-111268067	U87	brain:	n/a
20	chr13:111267935-111267985	NT2-D1	testis:	n/a
21	chr13:111288583-111288633	NH-A	brain:	n/a
22	chr13:111250832-111250882	NHBE	bronchial:	n/a
23	chr13:111288822-111288872	MCF10A-Er-Src	breast:	n/a
24	chr13:111250951-111251001	HRCEpiC	kidney:	n/a
25	chr13:111291685-111291735	HRPEpiC	eye:	n/a
26	chr13:111281479-111281529	GM12892	blood:	n/a
27	chr13:111268705-111268755	SK-N-SH	brain:	n/a
28	chr13:111281479-111281529	HNPCEpiC	eye:	n/a
29	chr13:111288257-111288307	AG10803	skin:	n/a
30	chr13:111267830-111267880	SK-N-SH_RA	brain:	n/a
31	chr13:111281144-111281194	HPAEpiC	pulmonary alveolar:	n/a
32	chr13:111288583-111288633	SK-N-SH_RA	brain:	n/a
33	chr13:111268673-111268723	MCF10A-Er-Src	breast:	n/a
34	chr13:111267793-111267843	SK-N-SH	brain:	n/a
35	chr13:111267830-111267880	GM19239	blood:	n/a
36	chr13:111268673-111268723	NB4	blood:	n/a
37	chr13:111275214-111275264	MCF-7	breast:	n/a
38	chr13:111291955-111292005	HCPEpiC	choroid plexus:	n/a
39	chr13:111270991-111271041	AG10803	skin:	n/a
40	chr13:111268702-111268752	Hepatocyte	liver:	n/a
41	chr13:111267849-111267899	NT2-D1	testis:	n/a
42	chr13:111285565-111285615	Hepatocyte	liver:	n/a
43	chr13:111287944-111287994	HAEpiC	amniotic membrane:	n/a
44	chr13:111281384-111281434	AG04449	skin:	fetal
45	chr13:111267830-111267880	Hepatocyte	liver:	n/a
46	chr13:111268031-111268081	NHBE	bronchial:	n/a
47	chr13:111288257-111288307	Caco-2	colon:	n/a
48	chr13:111267790-111267840	AoSMC	blood vessel:	n/a
49	chr13:111288032-111288082	U87	brain:	n/a
50	chr13:111288257-111288307	HMEC	breast:	n/a

(count:90 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr13:111241754..111244735-chr13:111266379..111269807,3	MCF-7	breast:
2	chr13:111160586..111163300-chr13:111242800..111244422,2	MCF-7	breast:
3	chr13:111266306..111273367-chr13:111274094..111280494,12	K562	blood:
4	chr13:111277332..111280156-chr13:111289105..111290945,2	MCF-7	breast:
5	chr13:111211148..111213368-chr13:111243811..111245903,2	MCF-7	breast:
6	chr13:111266746..111269387-chr13:111357064..111359748,3	MCF-7	breast:
7	chr13:111278124..111281264-chr13:111364873..111369262,5	MCF-7	breast:
8	chr13:111266965..111271727-chr13:111364973..111369025,9	MCF-7	breast:
9	chr13:111248805..111250322-chr13:111277318..111279178,2	MCF-7	breast:
10	chr13:111248410..111250824-chr13:111273874..111275589,2	MCF-7	breast:
11	chr13:111267955..111269613-chr13:111288415..111289925,2	K562	blood:
12	chr13:111284778..111286525-chr13:111522479..111525295,2	K562	blood:
13	chr13:111271645..111274603-chr13:111290397..111292824,3	MCF-7	breast:
14	chr13:111268021..111270238-chr13:111291368..111294151,2	MCF-7	breast:
15	chr13:111268040..111269954-chr13:111270156..111273298,3	K562	blood:
16	chr13:111287671..111291034-chr13:111291640..111294816,4	MCF-7	breast:
17	chr13:111270148..111271814-chr13:111272109..111273731,2	K562	blood:
18	chr13:111246094..111246720-chr13:111297267..111298158,2	MCF-7	breast:
19	chr13:111262131..111264525-chr13:111366020..111367721,2	MCF-7	breast:
20	chr13:111289947..111291840-chr13:111364201..111367983,3	MCF-7	breast:
21	chr13:111106850..111109675-chr13:111241801..111244096,2	MCF-7	breast:
22	chr13:111213298..111215293-chr13:111263862..111265630,2	MCF-7	breast:
23	chr13:111280796..111283636-chr13:111367642..111369332,2	K562	blood:
24	chr13:111267467..111269967-chr13:111564590..111568374,3	MCF-7	breast:
25	chr13:111254714..111256748-chr13:111263044..111265156,2	K562	blood:
26	chr13:111272905..111274580-chr13:111366963..111368758,2	MCF-7	breast:
27	chr13:111267921..111270163-chr13:111289347..111290890,2	MCF-7	breast:
28	chr13:111281708..111283812-chr13:111291061..111293411,2	K562	blood:
29	chr13:111247650..111249688-chr13:111251638..111253737,2	K562	blood:
30	chr13:111271154..111277326-chr13:111363993..111367812,9	K562	blood:
31	chr12:51157105..51157794-chr13:111267888..111268432,2	Hela-S3	cervix:
32	chr13:111267596..111269197-chr13:111364131..111366094,2	K562	blood:
33	chr13:111287003..111289809-chr13:111566070..111568939,2	K562	blood:
34	chr13:111248410..111250824-chr13:111273874..111275589,2	MCF-7	breast:
35	chr13:111248203..111253078-chr13:111266905..111270322,4	K562	blood:
36	chr13:111226642..111228664-chr13:111251915..111253703,2	MCF-7	breast:
37	chr13:111268194..111268777-chr6:12010640..12011635,2	Hela-S3	cervix:
38	chr13:111266604..111270536-chr13:111275017..111281975,10	MCF-7	breast:
39	chr13:111282173..111283948-chr13:111364006..111365721,2	K562	blood:
40	chr13:111266587..111269692-chr13:111357018..111359356,4	K562	blood:
41	chr13:111249993..111251646-chr13:111251671..111254443,2	MCF-7	breast:
42	chr13:111285638..111287730-chr13:111364678..111367940,3	MCF-7	breast:
43	chr13:111280819..111283163-chr13:111298869..111301563,3	K562	blood:
44	chr13:111287423..111289848-chr13:111365878..111368153,2	MCF-7	breast:
45	chr13:111266314..111268979-chr13:111280505..111282766,2	K562	blood:
46	chr13:111266737..111268751-chr13:111366724..111368921,2	K562	blood:
47	chr13:111288106..111291537-chr13:111365021..111367152,3	K562	blood:
48	chr13:111254714..111256748-chr13:111263044..111265156,2	K562	blood:
49	chr13:111270127..111273388-chr13:111363315..111367711,4	MCF-7	breast:
50	chr13:111267350..111267981-chr17:56756502..56757440,2	NB4	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CARKD-1	chr13:111291555-111292340	NONHSAT035156

No data

Variant related genes	Relation type
ENSG00000255831	TF binding region
CARKD	TF binding region
ENSG00000255831	CpG island
CARKD	CpG island
ENSG00000050405	chromatin interactions
ENSG00000181929	chromatin interactions
ENSG00000132510	chromatin interactions
ENSG00000153487	chromatin interactions
ENSG00000200997	chromatin interactions
ENSG00000134905	chromatin interactions
ENSG00000124151	chromatin interactions
ENSG00000104518	chromatin interactions
ENSG00000134871	chromatin interactions
ENSG00000213995	chromatin interactions
ENSG00000123268	chromatin interactions
ENSG00000196177	chromatin interactions
ENSG00000151422	chromatin interactions
ENSG00000139832	chromatin interactions
ENSG00000088448	chromatin interactions
ENSG00000255831	chromatin interactions

Extended variants
information (count: 2646 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:2646 , 50 per page) page: 1 2 3 4 5 6 7 ... 53

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9521853	chr13:111237260-111237261	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs9521854	chr13:111237313-111237314	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs75171647	chr13:111237330-111237331	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs9588197	chr13:111237334-111237335	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs113944024	chr13:111237416-111237417	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs554895092	chr13:111237479-111237480	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs141878459	chr13:111237480-111237481	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs187335918	chr13:111237491-111237492	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs193187695	chr13:111237492-111237493	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs577324805	chr13:111237530-111237531	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs8000878	chr13:111237551-111237552	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs146124711	chr13:111237586-111237587	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs547878610	chr13:111237602-111237603	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs530311317	chr13:111237648-111237649	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs8001230	chr13:111237659-111237660	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs373674637	chr13:111237706-111237707	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs560322056	chr13:111237716-111237717	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs527930781	chr13:111237728-111237729	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs552470439	chr13:111237768-111237769	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs570898191	chr13:111237769-111237770	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs201257601	chr13:111237815-111237816	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs8001575	chr13:111237831-111237832	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs8001585	chr13:111237847-111237848	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs569896717	chr13:111237857-111237858	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs568900465	chr13:111237880-111237881	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs536357639	chr13:111237923-111237924	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs554757947	chr13:111237955-111237956	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs185463088	chr13:111237974-111237975	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs190704134	chr13:111237975-111237976	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs534044173	chr13:111238044-111238045	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs60991631	chr13:111238059-111238060	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs115510605	chr13:111238070-111238071	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs544326676	chr13:111238126-111238127	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs556609248	chr13:111238136-111238137	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs117976068	chr13:111238137-111238138	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs555304629	chr13:111238138-111238139	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs116370805	chr13:111238156-111238157	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs560283272	chr13:111238251-111238252	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs12428407	chr13:111238336-111238337	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs546069776	chr13:111238359-111238360	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs564489381	chr13:111238361-111238362	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs192174453	chr13:111238369-111238370	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs12428421	chr13:111238374-111238375	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs149873518	chr13:111238378-111238379	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs76424201	chr13:111238384-111238385	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs568838520	chr13:111238400-111238401	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs529727144	chr13:111238401-111238402	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs548322378	chr13:111238469-111238470	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs566654538	chr13:111238513-111238514	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs375191273	chr13:111238527-111238528	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:92)

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
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
Neuroblastoma	18923191	CNVD
Ovarian cancer	22174824	CNVD
Myoepithelioma	18604193	CNVD
Breast cancer	17133270	CNVD
Prostate cancer	18632612	CNVD
Melanoma	18172304	CNVD
Prostate cancer	16573809	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Basal cell lymphoma	17053054	CNVD
Gastric cancer	17908304	CNVD
Liposarcoma	21253554	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Acute myeloid leukemia	20729466	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
Breast cancer	22032731	CNVD
Wilms tumour	21544195	CNVD
Thyroid cancer	19087340	CNVD
abortions and stillbirths	19751515	CNVD
Acute myeloid leukemia	21251322	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Burkitt''s lymphoma	20823134	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Burkitt''s lymphoma	19759907	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Medulloblastoma	19270706	CNVD
Mental retardation	17124404	CNVD
Leukemia	18688285	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21858162	CNVD
Melanoma	17363583	CNVD
Developmental delay	21147756	CNVD
Breast cancer	21364760	CNVD
Colorectal cancer	21645411	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Breast cancer	16608533	CNVD
Glioblastoma multiforme	22286061	CNVD
Follicular lymphoma	20505157	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
abnormal development	18461090	CNVD
Malignant glioma	17146433	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Glioma	17123091	CNVD
Sudden cardiac death	19188705	CNVD
Breast cancer	20409316	CNVD
Central neurocytomas	17123091	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Neurocytoma	17123091	CNVD
Mantle cell lymphoma	19029149	CNVD
Multiple myeloma	16616336	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1819 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:111228600-111243000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr13:111235800-111242000	Weak transcription	HepG2	liver
3	chr13:111240400-111240600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr13:111240800-111242200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr13:111242000-111242800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr13:111242000-111243400	Enhancers	HepG2	liver
7	chr13:111242200-111242800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
8	chr13:111242200-111243000	Enhancers	Adipose Nuclei	Adipose
9	chr13:111242200-111243200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr13:111242200-111243600	Enhancers	Breast Myoepithelial Primary Cells	Breast
11	chr13:111242200-111243800	Enhancers	HMEC	breast
12	chr13:111242400-111242800	Enhancers	K562	blood
13	chr13:111242400-111243000	Enhancers	NHEK	skin
14	chr13:111242400-111243200	Enhancers	ES-I3 Cell Line	embryonic stem cell
15	chr13:111242400-111243600	Enhancers	Placenta	Placenta
16	chr13:111242600-111243200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
17	chr13:111242600-111243200	Enhancers	HUES48 Cell Line	embryonic stem cell
18	chr13:111242600-111243200	Enhancers	Stomach Mucosa	stomach
19	chr13:111242600-111243400	Enhancers	HUES6 Cell Line	embryonic stem cell
20	chr13:111242600-111243400	Enhancers	HUES64 Cell Line	embryonic stem cell
21	chr13:111242600-111243400	Enhancers	iPS-18 Cell Line	embryonic stem cell
22	chr13:111242600-111243400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
23	chr13:111242600-111243600	Enhancers	iPS-15b Cell Line	embryonic stem cell
24	chr13:111242600-111243600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
25	chr13:111242600-111243800	Enhancers	Rectal Smooth Muscle	rectum
26	chr13:111242600-111244000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
27	chr13:111242600-111244200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
28	chr13:111242800-111243400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
29	chr13:111242800-111243600	Enhancers	Placenta Amnion	Placenta Amnion
30	chr13:111242800-111244800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
31	chr13:111242800-111244800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
32	chr13:111243000-111243400	Enhancers	H1 Cell Line	embryonic stem cell
33	chr13:111243000-111243400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
34	chr13:111243000-111243400	Enhancers	Pancreas	Pancrea
35	chr13:111243000-111243400	Flanking Active TSS	NHEK	skin
36	chr13:111243000-111243600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
37	chr13:111243200-111243400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
38	chr13:111243200-111254400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
39	chr13:111243400-111243800	Enhancers	NHEK	skin
40	chr13:111243400-111249200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
41	chr13:111243600-111245200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
42	chr13:111243600-111249600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
43	chr13:111243800-111244800	Weak transcription	NHEK	skin
44	chr13:111243800-111245000	Weak transcription	HMEC	breast
45	chr13:111244000-111249400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
46	chr13:111244200-111244600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
47	chr13:111244600-111245000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
48	chr13:111244600-111245200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
49	chr13:111244600-111245400	Enhancers	Osteobl	bone
50	chr13:111244800-111245000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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