Variant report

Variant	esv3344877
Chromosome Location	chr15:83294946-83316565
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:438)
CpG islands
(count:671)
Chromatin interactive
region (count:28)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:438 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:83304545-83304986	K562	blood:	n/a	n/a
2	ARID3A	chr15:83312830-83313239	K562	blood:	n/a	n/a
3	ARID3A	chr15:83316181-83316371	K562	blood:	n/a	n/a
4	ATF1	chr15:83309450-83309802	K562	blood:	n/a	n/a
5	ATF3	chr15:83316247-83316595	K562	blood:	n/a	chr15:83316499-83316508 chr15:83316463-83316483
6	BACH1	chr15:83315055-83315175	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr15:83313561-83313573	K562	blood:	n/a	n/a
8	BACH1	chr15:83315444-83315541	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr15:83316299-83316507	K562	blood:	n/a	n/a
10	BACH1	chr15:83316360-83316560	H1-hESC	embryonic stem cell:	n/a	n/a
11	BCLAF1	chr15:83315909-83316668	K562	blood:	n/a	chr15:83316212-83316225 chr15:83316358-83316371 chr15:83316362-83316375 chr15:83316366-83316379 chr15:83316500-83316509 chr15:83316349-83316362
12	BHLHE40	chr15:83314933-83316809	K562	blood:	n/a	chr15:83316462-83316471 chr15:83316461-83316474 chr15:83316463-83316472 chr15:83316464-83316473 chr15:83316463-83316472
13	BHLHE40	chr15:83316127-83316639	A549	lung:	n/a	chr15:83316462-83316471 chr15:83316461-83316474 chr15:83316463-83316472 chr15:83316464-83316473 chr15:83316463-83316472
14	BHLHE40	chr15:83298789-83299129	K562	blood:	n/a	n/a
15	BHLHE40	chr15:83316271-83316623	GM12878	blood:	n/a	chr15:83316462-83316471 chr15:83316461-83316474 chr15:83316463-83316472 chr15:83316464-83316473 chr15:83316463-83316472
16	BHLHE40	chr15:83304624-83304939	K562	blood:	n/a	n/a
17	BHLHE40	chr15:83316236-83316620	HepG2	liver:	n/a	chr15:83316462-83316471 chr15:83316461-83316474 chr15:83316463-83316472 chr15:83316464-83316473 chr15:83316463-83316472
18	BHLHE40	chr15:83314053-83314289	K562	blood:	n/a	n/a
19	CBX3	chr15:83314073-83314488	K562	blood:	n/a	n/a
20	CBX3	chr15:83314795-83316810	K562	blood:	n/a	n/a
21	CBX3	chr15:83315656-83316152	K562	blood:	n/a	n/a
22	CCNT2	chr15:83315005-83317012	K562	blood:	n/a	chr15:83315968-83315977
23	CCNT2	chr15:83304603-83304898	K562	blood:	n/a	n/a
24	CCNT2	chr15:83313384-83313588	K562	blood:	n/a	n/a
25	CEBPB	chr15:83310707-83310891	HepG2	liver:	n/a	chr15:83310785-83310796
26	CEBPB	chr15:83315883-83315997	H1-hESC	embryonic stem cell:	n/a	n/a
27	CEBPB	chr15:83312757-83313121	K562	blood:	n/a	n/a
28	CEBPB	chr15:83310674-83310955	A549	lung:	n/a	chr15:83310785-83310796
29	CEBPD	chr15:83304464-83304882	K562	blood:	n/a	n/a
30	CHD1	chr15:83315365-83315366	H1-hESC	embryonic stem cell:	n/a	n/a
31	CHD2	chr15:83315104-83315365	K562	blood:	n/a	chr15:83315209-83315219 chr15:83315200-83315210
32	CHD2	chr15:83315607-83315660	K562	blood:	n/a	n/a
33	CHD2	chr15:83315866-83316736	K562	blood:	n/a	chr15:83316377-83316384
34	CHD2	chr15:83314390-83314759	K562	blood:	n/a	n/a
35	CREB1	chr15:83316110-83317150	A549	lung:	n/a	n/a
36	CTCF	chr15:83316100-83316250	HEK293	kidney:	n/a	n/a
37	CTCF	chr15:83316140-83316290	AoAF	blood vessel:	n/a	n/a
38	CTCF	chr15:83316160-83316310	HPAF	blood vessel:	n/a	n/a
39	CTCF	chr15:83316020-83316170	HRE	kidney:	n/a	n/a
40	CTCF	chr15:83316080-83316230	HRPEpiC	eye:	n/a	n/a
41	CTCF	chr15:83316140-83316290	SK-N-SH_RA	brain:	n/a	n/a
42	CTCF	chr15:83316100-83316250	HCM	heart:	n/a	n/a
43	CTCF	chr15:83316180-83316330	GM12866	blood:	n/a	n/a
44	CTCF	chr15:83316020-83316170	SAEC	small airway:	n/a	n/a
45	CTCF	chr15:83316120-83316270	NHLF	lung:	n/a	n/a
46	CTCF	chr15:83299988-83300065	GM13976	blood:	n/a	n/a
47	CTCF	chr15:83316132-83316260	MCF-7	breast:	n/a	n/a
48	CTCF	chr15:83316120-83316270	AG04449	skin:	n/a	n/a
49	CTCF	chr15:83315900-83316050	NHLF	lung:	n/a	n/a
50	CTCF	chr15:83315947-83316667	A549	lung:	n/a	n/a

(count:671 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:83314985-83315035	H1-hESC	embryonic stem cell:	embryo
2	chr15:83298969-83299019	GM12892	blood:	n/a
3	chr15:83316223-83316273	AoSMC	blood vessel:	n/a
4	chr15:83298692-83298742	MCF10A-Er-Src	breast:	n/a
5	chr15:83316378-83316428	HCM	heart:	n/a
6	chr15:83298969-83299019	HepG2	liver:	n/a
7	chr15:83315627-83315677	GM19239	blood:	n/a
8	chr15:83315615-83315665	AoSMC	blood vessel:	n/a
9	chr15:83316378-83316428	SKMC	muscle:	n/a
10	chr15:83312439-83312489	ProgFib	skin:	n/a
11	chr15:83315922-83315972	A549	lung:	n/a
12	chr15:83315922-83315972	T-47D	breast:	n/a
13	chr15:83312439-83312489	HNPCEpiC	eye:	n/a
14	chr15:83298692-83298742	U87	brain:	n/a
15	chr15:83315627-83315677	ECC-1	luminal epithelium:	n/a
16	chr15:83297312-83297362	HRPEpiC	eye:	n/a
17	chr15:83298692-83298742	HRPEpiC	eye:	n/a
18	chr15:83298969-83299019	HCM	heart:	n/a
19	chr15:83315627-83315677	NT2-D1	testis:	n/a
20	chr15:83315922-83315972	K562	blood:	n/a
21	chr15:83316223-83316273	AG10803	skin:	n/a
22	chr15:83316223-83316273	BJ	skin:	n/a
23	chr15:83315627-83315677	PANC-1	pancreas:	n/a
24	chr15:83298692-83298742	Hela-S3	cervix:	n/a
25	chr15:83300338-83300388	HEK293	kidney:	embryo
26	chr15:83298969-83299019	GM19239	blood:	n/a
27	chr15:83316378-83316428	NB4	blood:	n/a
28	chr15:83314985-83315035	LNCaP	prostate:	n/a
29	chr15:83316378-83316428	HRPEpiC	eye:	n/a
30	chr15:83315615-83315665	HRPEpiC	eye:	n/a
31	chr15:83316223-83316273	NB4	blood:	n/a
32	chr15:83298969-83299019	ProgFib	skin:	n/a
33	chr15:83315627-83315677	AG04450	lung:	fetal
34	chr15:83298969-83299019	HCPEpiC	choroid plexus:	n/a
35	chr15:83314985-83315035	HMEC	breast:	n/a
36	chr15:83315615-83315665	BJ	skin:	n/a
37	chr15:83315615-83315665	HRCEpiC	kidney:	n/a
38	chr15:83316378-83316428	SK-N-SH	brain:	n/a
39	chr15:83312439-83312489	AG09319	gingival:	n/a
40	chr15:83298969-83299019	HEK293	kidney:	embryo
41	chr15:83315627-83315677	AoSMC	blood vessel:	n/a
42	chr15:83316223-83316273	HRCEpiC	kidney:	n/a
43	chr15:83316223-83316273	HL-60	blood:	n/a
44	chr15:83314985-83315035	SK-N-SH_RA	brain:	n/a
45	chr15:83316223-83316273	GM12878	blood:	n/a
46	chr15:83312439-83312489	HCM	heart:	n/a
47	chr15:83312439-83312489	ECC-1	luminal epithelium:	n/a
48	chr15:83312439-83312489	AG10803	skin:	n/a
49	chr15:83312439-83312489	LNCaP	prostate:	n/a
50	chr15:83297312-83297362	MCF-7	breast:	n/a

(count:28 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:83301754..83304309-chr15:83307925..83309432,2	MCF-7	breast:
2	chr15:83216717..83218665-chr15:83313410..83315739,2	K562	blood:
3	chr15:83315715..83320562-chr15:83347753..83351536,6	K562	blood:
4	chr15:83311716..83313407-chr15:83348660..83350987,2	MCF-7	breast:
5	chr15:83315484..83318072-chr15:83348095..83350570,4	MCF-7	breast:
6	chr15:83296579..83300038-chr15:83302412..83305627,3	K562	blood:
7	chr15:83316185..83318129-chr15:83417608..83419750,3	K562	blood:
8	chr15:83314747..83316448-chr15:83680031..83681739,2	K562	blood:
9	chr15:83225687..83228641-chr15:83313130..83314679,2	K562	blood:
10	chr15:83314418..83317134-chr15:83417560..83419673,2	MCF-7	breast:
11	chr15:83315603..83319675-chr15:83327659..83331605,4	K562	blood:
12	chr15:83304208..83306459-chr15:83417486..83420687,3	K562	blood:
13	chr15:83313668..83318129-chr15:83416864..83421207,8	K562	blood:
14	chr15:83292844..83294739-chr15:83312087..83314225,2	K562	blood:
15	chr15:83238728..83241001-chr15:83305797..83309548,3	K562	blood:
16	chr15:83290488..83293099-chr15:83294149..83296751,2	K562	blood:
17	chr15:83311482..83314245-chr15:83326104..83328950,2	K562	blood:
18	chr15:83313427..83317808-chr15:83477553..83483000,6	K562	blood:
19	chr15:83293051..83295110-chr15:83315019..83317185,2	K562	blood:
20	chr15:83316099..83317759-chr15:83406962..83409710,2	K562	blood:
21	chr15:83276398..83279103-chr15:83299744..83301374,2	K562	blood:
22	chr15:83294774..83297381-chr15:83349087..83350883,2	MCF-7	breast:
23	chr15:83296467..83300526-chr15:83302412..83306697,6	K562	blood:
24	chr15:83311386..83314331-chr15:83366792..83368787,2	K562	blood:
25	chr15:83293051..83295658-chr15:83314661..83316519,2	K562	blood:
26	chr15:83301754..83304309-chr15:83307925..83309432,2	MCF-7	breast:
27	chr15:83309961..83312458-chr15:83331065..83333558,2	K562	blood:
28	chr15:83313759..83319278-chr15:83347483..83351536,8	K562	blood:

(count:9 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-379H8.1.1-1	chr15:83316521-83317559	ENSG00000259462.1
2	lnc-RP11-379H8.1.1-3	chr15:83295315-83295451	l_1205_chr15:83293110-83297075_liver
3	lnc-CPEB1-1	chr15:83296040-83296118	NONHSAT047839
4	lnc-RP11-379H8.1.1-3	chr15:83296489-83297075	l_1205_chr15:83293110-83297075_liver
5	lnc-AP3B2-2	chr15:83309408-83309616	NONHSAT047840
6	lnc-AP3B2-2	chr15:83301933-83301972	NONHSAT047840
7	lnc-AP3B2-2	chr15:83307316-83307385	NONHSAT047840
8	lnc-AP3B2-2	chr15:83310376-83310433	NONHSAT047840
9	lnc-RP11-379H8.1.1-1	chr15:83316521-83317559	ENSG00000244937

No data

Variant related genes	Relation type
CPEB1	TF binding region
ENSG00000259462	TF binding region
CPEB1	CpG island
ENSG00000259462	CpG island
ENSG00000260608	chromatin interactions
ENSG00000214575	chromatin interactions
ENSG00000156232	chromatin interactions
ENSG00000169609	chromatin interactions
ENSG00000103723	chromatin interactions
ENSG00000250988	chromatin interactions
ENSG00000259315	chromatin interactions
ENSG00000259462	chromatin interactions
BCKDHB	miRNA target sites

Extended variants
information (count: 851 )
Associated
traits (count: 63 )

Variant overlapped rSNPs/rCNVs (count:851 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs535153424	chr15:83294959-83294960	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs140199352	chr15:83294963-83294964	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs546796134	chr15:83294978-83294979	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs150312031	chr15:83294987-83294988	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs537732008	chr15:83295002-83295003	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs191553705	chr15:83295053-83295054	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs201348635	chr15:83295077-83295078	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs571685186	chr15:83295100-83295101	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs565885629	chr15:83295116-83295117	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs545789581	chr15:83295117-83295118	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs373989343	chr15:83295121-83295122	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs184122028	chr15:83295140-83295141	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs188911251	chr15:83295163-83295164	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs199695621	chr15:83295193-83295194	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs71412265	chr15:83295216-83295217	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs2870966	chr15:83295244-83295245	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
17	rs561728014	chr15:83295266-83295267	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs530656678	chr15:83295336-83295337	Weak transcription Strong transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
19	rs544009987	chr15:83295384-83295385	Weak transcription Strong transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
20	rs563992099	chr15:83295396-83295397	Weak transcription Strong transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
21	rs192294326	chr15:83295432-83295433	Weak transcription Strong transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
22	rs552254937	chr15:83295436-83295437	Weak transcription Strong transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
23	rs140769723	chr15:83295456-83295457	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs528573338	chr15:83295491-83295492	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs548702606	chr15:83295550-83295551	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs568575484	chr15:83295551-83295552	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs113067906	chr15:83295561-83295562	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs528032965	chr15:83295614-83295615	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs571122479	chr15:83295669-83295670	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs540163404	chr15:83295711-83295712	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs552674259	chr15:83295712-83295713	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs545379515	chr15:83295718-83295719	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs144590923	chr15:83295744-83295745	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs535192351	chr15:83295812-83295813	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs555401777	chr15:83295817-83295818	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs138778202	chr15:83295828-83295829	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs543975001	chr15:83295835-83295836	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs563955483	chr15:83295844-83295845	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs149322138	chr15:83295894-83295895	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs369595604	chr15:83295926-83295927	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs373688655	chr15:83295940-83295941	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs369500861	chr15:83295960-83295961	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs377521130	chr15:83296019-83296020	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs200431699	chr15:83296031-83296032	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs370977022	chr15:83296037-83296038	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs374349658	chr15:83296057-83296058	Weak transcription Strong transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
47	rs376164471	chr15:83296058-83296059	Weak transcription Strong transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
48	rs370569656	chr15:83296063-83296064	Weak transcription Strong transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
49	rs61733713	chr15:83296073-83296074	Weak transcription Strong transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
50	rs528444931	chr15:83296094-83296095	Weak transcription Strong transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:63)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	CNVD
Wilms tumour	21544195	CNVD
cataract	16735990	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Medulloblastoma	21979893	CNVD
spastic paraplegia with thinning of corpus callosum	19105190	CNVD
Schizophrenia	21324950	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Disease	21824424	CNVD
Melanoma	18172304	CNVD
Gastric cancer	17167181	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Colorectal cancer	16272173	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Multiple myeloma	17550852	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Multiple myeloma	20724749	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Prostate cancer	18632612	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Cancer	16751803	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Autism	17322880	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Lung cancer	18438408	CNVD
Papillary thyroid carcinoma	22161024	CNVD
Autism	21480499	CNVD
Breast cancer	17603634	CNVD
Acute myeloid leukemia	16864856	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
small cell lung cancer	20016488	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Colorectal cancer	16774939	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Sudden cardiac death	19188705	CNVD
abnormal development	18461090	CNVD
Intellectual disability	22102821	CNVD
renal disease	17924346	CNVD
Breast cancer	20409316	CNVD
Mental retardation	17847001	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21785460	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:399 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:83241800-83297600	Weak transcription	Brain Inferior Temporal Lobe	brain
2	chr15:83282800-83312800	Weak transcription	Brain Hippocampus Middle	brain
3	chr15:83287600-83296600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr15:83288800-83297000	Weak transcription	Brain Substantia Nigra	brain
5	chr15:83290600-83296800	Weak transcription	Brain Angular Gyrus	brain
6	chr15:83291400-83297600	Weak transcription	Brain Cingulate Gyrus	brain
7	chr15:83292800-83298800	Strong transcription	K562	blood
8	chr15:83294200-83296800	Weak transcription	Brain Anterior Caudate	brain
9	chr15:83296600-83297400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr15:83296800-83297400	Enhancers	Brain Angular Gyrus	brain
11	chr15:83297000-83297200	Enhancers	Brain Substantia Nigra	brain
12	chr15:83297400-83300800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr15:83298800-83299000	Genic enhancers	K562	blood
14	chr15:83299000-83299600	Enhancers	K562	blood
15	chr15:83299600-83302200	Weak transcription	K562	blood
16	chr15:83301600-83301800	Enhancers	Fetal Kidney	kidney
17	chr15:83302200-83302600	Enhancers	K562	blood
18	chr15:83302600-83303800	Weak transcription	K562	blood
19	chr15:83303800-83304400	Enhancers	K562	blood
20	chr15:83304400-83305000	Flanking Active TSS	K562	blood
21	chr15:83305000-83305800	Enhancers	K562	blood
22	chr15:83305800-83307600	Weak transcription	K562	blood
23	chr15:83306200-83306400	Bivalent Enhancer	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
24	chr15:83306200-83306400	Enhancers	Pancreas	Pancrea
25	chr15:83306400-83315000	Weak transcription	Pancreas	Pancrea
26	chr15:83306800-83307200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
27	chr15:83307600-83309800	Genic enhancers	K562	blood
28	chr15:83308800-83310400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
29	chr15:83309200-83310400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
30	chr15:83309400-83309600	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
31	chr15:83309400-83310600	Enhancers	ES-I3 Cell Line	embryonic stem cell
32	chr15:83309600-83310400	Enhancers	Skeletal Muscle Male	skeletal muscle
33	chr15:83309800-83310400	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
34	chr15:83309800-83312600	Enhancers	K562	blood
35	chr15:83310000-83310200	Enhancers	Brain Anterior Caudate	brain
36	chr15:83310000-83310400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
37	chr15:83310000-83310400	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
38	chr15:83310000-83310400	Bivalent Enhancer	Skeletal Muscle Female	skeletal muscle
39	chr15:83310200-83310400	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
40	chr15:83310200-83312800	Weak transcription	Brain Anterior Caudate	brain
41	chr15:83310400-83311600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
42	chr15:83310400-83312600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
43	chr15:83310600-83311000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
44	chr15:83310600-83312600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
45	chr15:83311800-83312000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
46	chr15:83312400-83312800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
47	chr15:83312400-83314000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
48	chr15:83312600-83312800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
49	chr15:83312600-83312800	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
50	chr15:83312600-83313000	Bivalent Enhancer	Ganglion Eminence derived primary cultured neurospheres	brain

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