Variant report

Variant	esv35150
Chromosome Location	chr15:56677730-56896304
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1328)
CpG islands
(count:915)
Chromatin interactive
region (count:46)
LncRNA
region (count:13)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1328 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:56721089-56721405	K562	blood:	n/a	n/a
2	ARID3A	chr15:56757439-56757589	K562	blood:	n/a	n/a
3	ARID3A	chr15:56757183-56757342	HepG2	liver:	n/a	n/a
4	ARID3A	chr15:56788752-56789118	HepG2	liver:	n/a	chr15:56788814-56788830
5	ARID3A	chr15:56881619-56881703	K562	blood:	n/a	n/a
6	ARID3A	chr15:56788756-56789177	K562	blood:	n/a	chr15:56788814-56788830
7	ATF1	chr15:56761692-56762037	K562	blood:	n/a	n/a
8	ATF1	chr15:56701414-56701616	K562	blood:	n/a	n/a
9	ATF1	chr15:56785297-56785306	K562	blood:	n/a	n/a
10	ATF2	chr15:56757025-56757555	GM12878	blood:	n/a	n/a
11	ATF3	chr15:56767569-56767875	K562	blood:	n/a	n/a
12	BACH1	chr15:56757137-56757703	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr15:56757918-56757978	K562	blood:	n/a	n/a
14	BATF	chr15:56788822-56789212	GM12878	blood:	n/a	n/a
15	BCL3	chr15:56757103-56757795	A549	lung:	n/a	n/a
16	BCL3	chr15:56757037-56757647	GM12878	blood:	n/a	n/a
17	BCLAF1	chr15:56757083-56757625	GM12878	blood:	n/a	n/a
18	BHLHE40	chr15:56757184-56757611	K562	blood:	n/a	chr15:56757254-56757270
19	BHLHE40	chr15:56830099-56830356	GM12878	blood:	n/a	n/a
20	BHLHE40	chr15:56783358-56783670	GM12878	blood:	n/a	n/a
21	BHLHE40	chr15:56704886-56704981	GM12878	blood:	n/a	n/a
22	BHLHE40	chr15:56844843-56845124	K562	blood:	n/a	n/a
23	BHLHE40	chr15:56757494-56757730	HepG2	liver:	n/a	n/a
24	CBX3	chr15:56878477-56878666	K562	blood:	n/a	n/a
25	CBX3	chr15:56878353-56878826	HCT-116	colon:	n/a	n/a
26	CBX3	chr15:56878445-56878784	K562	blood:	n/a	n/a
27	CBX3	chr15:56757101-56757760	K562	blood:	n/a	n/a
28	CBX3	chr15:56757309-56757702	K562	blood:	n/a	n/a
29	CCNT2	chr15:56757151-56757524	K562	blood:	n/a	n/a
30	CEBPB	chr15:56854262-56854583	HepG2	liver:	n/a	chr15:56854398-56854409
31	CEBPB	chr15:56687195-56687330	HepG2	liver:	n/a	chr15:56687247-56687258
32	CEBPB	chr15:56752307-56752555	K562	blood:	n/a	n/a
33	CEBPB	chr15:56767650-56767857	H1-hESC	embryonic stem cell:	n/a	chr15:56767741-56767752
34	CEBPB	chr15:56706437-56706660	A549	lung:	n/a	n/a
35	CEBPB	chr15:56724617-56724796	H1-hESC	embryonic stem cell:	n/a	chr15:56724724-56724735
36	CEBPB	chr15:56845033-56845203	K562	blood:	n/a	n/a
37	CEBPB	chr15:56715740-56715857	A549	lung:	n/a	n/a
38	CEBPB	chr15:56848778-56849077	Hela-S3	cervix:	n/a	chr15:56848952-56848963
39	CEBPB	chr15:56683119-56683285	A549	lung:	n/a	n/a
40	CEBPB	chr15:56828054-56828116	K562	blood:	n/a	n/a
41	CEBPB	chr15:56848678-56849081	HepG2	liver:	n/a	chr15:56848952-56848963
42	CEBPB	chr15:56724457-56724851	A549	lung:	n/a	chr15:56724724-56724735
43	CEBPB	chr15:56757311-56757566	K562	blood:	n/a	n/a
44	CEBPB	chr15:56841846-56842133	IMR90	lung:	n/a	n/a
45	CEBPB	chr15:56788854-56789190	IMR90	lung:	n/a	n/a
46	CEBPB	chr15:56708105-56708119	IMR90	lung:	n/a	n/a
47	CEBPB	chr15:56844926-56845294	Hela-S3	cervix:	n/a	n/a
48	CEBPB	chr15:56724449-56724866	HepG2	liver:	n/a	chr15:56724724-56724735
49	CEBPB	chr15:56788774-56789197	Hela-S3	cervix:	n/a	n/a
50	CEBPB	chr15:56845045-56845245	A549	lung:	n/a	n/a

(count:915 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:56759655-56759705	T-47D	breast:	n/a
2	chr15:56757290-56757340	NB4	blood:	n/a
3	chr15:56757314-56757364	HCPEpiC	choroid plexus:	n/a
4	chr15:56757312-56757362	LNCaP	prostate:	n/a
5	chr15:56757517-56757567	HRE	kidney:	n/a
6	chr15:56757806-56757856	HIPEpiC	eye:	n/a
7	chr15:56758270-56758320	U87	brain:	n/a
8	chr15:56759655-56759705	GM12891	blood:	n/a
9	chr15:56725876-56725926	Hepatocyte	liver:	n/a
10	chr15:56758270-56758320	HRE	kidney:	n/a
11	chr15:56757312-56757362	SKMC	muscle:	n/a
12	chr15:56757552-56757602	SAEC	small airway:	n/a
13	chr15:56757108-56757158	NT2-D1	testis:	n/a
14	chr15:56757290-56757340	Hela-S3	cervix:	n/a
15	chr15:56757806-56757856	GM12891	blood:	n/a
16	chr15:56757108-56757158	HCT-116	colon:	n/a
17	chr15:56757806-56757856	HUVEC	blood vessel:	n/a
18	chr15:56757312-56757362	GM12891	blood:	n/a
19	chr15:56757517-56757567	RPTEC	kidney:	n/a
20	chr15:56757552-56757602	HEEpiC	esophagus:	n/a
21	chr15:56757552-56757602	SKMC	muscle:	n/a
22	chr15:56757312-56757362	RPTEC	kidney:	n/a
23	chr15:56757312-56757362	MCF-7	breast:	n/a
24	chr15:56757290-56757340	BE2_C	brain:	n/a
25	chr15:56757517-56757567	HPAEpiC	pulmonary alveolar:	n/a
26	chr15:56725876-56725926	SK-N-SH_RA	brain:	n/a
27	chr15:56759655-56759705	HEK293	kidney:	embryo
28	chr15:56758270-56758320	HAEpiC	amniotic membrane:	n/a
29	chr15:56757325-56757375	HUVEC	blood vessel:	n/a
30	chr15:56757806-56757856	Caco-2	colon:	n/a
31	chr15:56757499-56757549	AoSMC	blood vessel:	n/a
32	chr15:56757552-56757602	AG04449	skin:	fetal
33	chr15:56757314-56757364	NB4	blood:	n/a
34	chr15:56757290-56757340	SAEC	small airway:	n/a
35	chr15:56758270-56758320	GM12891	blood:	n/a
36	chr15:56757312-56757362	GM12892	blood:	n/a
37	chr15:56758270-56758320	HRPEpiC	eye:	n/a
38	chr15:56757806-56757856	A549	lung:	n/a
39	chr15:56757290-56757340	AG10803	skin:	n/a
40	chr15:56757625-56757675	HIPEpiC	eye:	n/a
41	chr15:56757625-56757675	HCT-116	colon:	n/a
42	chr15:56757108-56757158	AoSMC	blood vessel:	n/a
43	chr15:56758270-56758320	Hela-S3	cervix:	n/a
44	chr15:56757625-56757675	PrEC	prostate:	n/a
45	chr15:56757517-56757567	H1-hESC	embryonic stem cell:	embryo
46	chr15:56725876-56725926	PrEC	prostate:	n/a
47	chr15:56759655-56759705	NHBE	bronchial:	n/a
48	chr15:56757499-56757549	HEEpiC	esophagus:	n/a
49	chr15:56757180-56757230	NHBE	bronchial:	n/a
50	chr15:56757325-56757375	NHDF-neo	bronchial:	n/a

(count:46 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:56540966..56543133-chr15:56718827..56720916,2	MCF-7	breast:
2	chr15:56731142..56732969-chr15:56736651..56738760,2	K562	blood:
3	chr15:56782685..56785505-chr15:57019755..57021681,2	K562	blood:
4	chr15:56787707..56790107-chr15:57597582..57600140,2	MCF-7	breast:
5	chr15:56537987..56538847-chr15:56756234..56756979,2	MCF-7	breast:
6	chr15:56537986..56539019-chr15:56720847..56721772,4	K562	blood:
7	chr15:56714747..56716284-chr15:56716589..56718483,2	MCF-7	breast:
8	chr15:56775436..56776246-chr15:56784313..56784975,2	K562	blood:
9	chr15:55940442..55941185-chr15:56720975..56721740,2	K562	blood:
10	chr15:56811740..56813746-chr15:56822934..56825907,2	K562	blood:
11	chr15:56788753..56789362-chr15:57161247..57161954,2	K562	blood:
12	chr15:56788688..56789403-chr15:57430424..57431057,2	MCF-7	breast:
13	chr15:56814069..56816681-chr15:56818491..56820321,2	K562	blood:
14	chr15:56538080..56538849-chr15:56720711..56721356,4	MCF-7	breast:
15	chr15:56788851..56789408-chr15:57103635..57104349,2	MCF-7	breast:
16	chr15:56587524..56588313-chr15:56720286..56721333,4	MCF-7	breast:
17	chr15:56762921..56765735-chr15:56765770..56767934,2	K562	blood:
18	chr15:56536734..56539507-chr15:56718886..56721172,2	MCF-7	breast:
19	chr15:56731142..56732969-chr15:56736651..56738760,2	K562	blood:
20	chr15:56788456..56789162-chr15:57113822..57114589,2	MCF-7	breast:
21	chr15:56788702..56789394-chr15:57161523..57162414,2	MCF-7	breast:
22	chr15:56817798..56822839-chr15:56825097..56828742,5	K562	blood:
23	chr15:56756734..56759056-chr15:56761429..56763544,2	K562	blood:
24	chr15:56791160..56793250-chr15:56794933..56796796,2	K562	blood:
25	chr15:56788444..56789415-chr15:57598413..57599206,3	K562	blood:
26	chr15:56696715..56699099-chr15:56700955..56702991,2	MCF-7	breast:
27	chr15:56817798..56822286-chr15:56825097..56828742,4	K562	blood:
28	chr15:56541018..56541999-chr15:56720733..56721455,3	MCF-7	breast:
29	chr15:56762921..56765735-chr15:56765770..56767934,2	K562	blood:
30	chr15:56791160..56793250-chr15:56794933..56796796,2	K562	blood:
31	chr15:56066629..56067204-chr15:56720771..56721659,2	K562	blood:
32	chr15:56536083..56538918-chr15:56762516..56765231,2	K562	blood:
33	chr15:56537725..56539025-chr15:56720287..56722326,16	MCF-7	breast:
34	chr15:56540398..56542023-chr15:56720800..56721752,16	MCF-7	breast:
35	chr15:56775436..56776246-chr15:56784313..56784975,2	K562	blood:
36	chr15:56814069..56816681-chr15:56818491..56820321,2	K562	blood:
37	chr15:56541012..56541917-chr15:56720826..56721341,2	K562	blood:
38	chr15:56697956..56699869-chr15:56701440..56703984,2	MCF-7	breast:
39	chr15:56811740..56813746-chr15:56822934..56825907,2	K562	blood:
40	chr15:56782970..56783589-chr15:57598753..57599463,2	MCF-7	breast:
41	chr15:56714747..56716284-chr15:56716589..56718483,2	MCF-7	breast:
42	chr15:56788863..56789371-chr16:34759996..34760825,2	MCF-7	breast:
43	chr15:56783040..56784156-chr15:57161563..57162645,6	K562	blood:
44	chr15:56773647..56776313-chr15:57177229..57179430,2	K562	blood:
45	chr15:56817798..56822286-chr15:56825097..56828742,4	K562	blood:
46	chr15:56817798..56822839-chr15:56825097..56828742,5	K562	blood:

(count:13 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF280D-1	chr15:56835757-56836010	ENSG00000260392.1
2	lnc-ZNF280D-1	chr15:56884918-56885050	ENSG00000260392.1
3	lnc-ZNF280D-2	chr15:56757168-56757283	NONHSAT044023
4	lnc-MNS1-1	chr15:56701994-56702384	ENSG00000261823.1
5	lnc-ZNF280D-1	chr15:56896038-56896069	ENSG00000260392.1
6	lnc-MNS1-1	chr15:56700681-56701128	ENSG00000261823.1
7	lnc-ZNF280D-1	chr15:56840136-56840205	ENSG00000260392.1
8	lnc-ZNF280D-1	chr15:56841355-56841708	ENSG00000260392.1
9	lnc-ZNF280D-1	chr15:56841355-56841708	ENSG00000260392.1
10	lnc-ZNF280D-1	chr15:56840058-56840205	ENSG00000260392.1
11	lnc-ZNF280D-1	chr15:56835150-56835294	ENSG00000260392.1
12	lnc-ZNF280D-1	chr15:56840645-56840799	ENSG00000260392.1
13	lnc-ZNF280D-2	chr15:56755978-56756445	NONHSAT044023

No data

Variant related genes	Relation type
ENSG00000259941	TF binding region
MNS1	TF binding region
TEX9	TF binding region
ENSG00000261823	TF binding region
ENSG00000259941	CpG island
MNS1	CpG island
TEX9	CpG island
ENSG00000261823	CpG island
ENSG00000151575	chromatin interactions
ENSG00000261823	chromatin interactions
ENSG00000138587	chromatin interactions

Extended variants
information (count: 7148 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:7148 , 50 per page) page: 1 2 3 4 5 6 7 ... 143

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12900678	chr15:56677730-56677731	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs377095586	chr15:56677821-56677822	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs541618544	chr15:56677862-56677863	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs34208099	chr15:56677874-56677875	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs150433475	chr15:56677952-56677953	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs567362866	chr15:56677958-56677959	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs192972027	chr15:56677962-56677963	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs72742619	chr15:56677963-56677964	ZNF genes & repeats Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs576340330	chr15:56677973-56677974	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs138257374	chr15:56678050-56678051	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs558859885	chr15:56678060-56678061	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs35396132	chr15:56678068-56678069	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs572242306	chr15:56678071-56678072	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs184175653	chr15:56678079-56678080	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs540633749	chr15:56678107-56678108	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs560243580	chr15:56678121-56678122	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs142961856	chr15:56678127-56678128	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs114899837	chr15:56678161-56678162	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs562623418	chr15:56678175-56678176	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs191266717	chr15:56678226-56678227	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs146140865	chr15:56678257-56678258	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs533429544	chr15:56678268-56678269	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs113766134	chr15:56678280-56678281	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs527938064	chr15:56678370-56678371	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs7163544	chr15:56678371-56678372	ZNF genes & repeats Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs567243014	chr15:56678392-56678393	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs8029000	chr15:56678475-56678476	ZNF genes & repeats Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs189360052	chr15:56678503-56678504	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs529283012	chr15:56678528-56678529	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs569764182	chr15:56678612-56678613	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs538868724	chr15:56678638-56678639	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs112936161	chr15:56678695-56678696	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs77127164	chr15:56678697-56678698	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs540941950	chr15:56678720-56678721	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs561994307	chr15:56678736-56678737	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs554155901	chr15:56678753-56678754	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs143887120	chr15:56678765-56678766	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs80351429	chr15:56678769-56678770	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs562686143	chr15:56678771-56678772	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs4142479	chr15:56678775-56678776	ZNF genes & repeats Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs545591480	chr15:56678807-56678808	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs565288233	chr15:56678846-56678847	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs78902598	chr15:56678869-56678870	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs76092725	chr15:56678876-56678877	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs561549930	chr15:56678877-56678878	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs73413960	chr15:56678888-56678889	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs549794217	chr15:56678980-56678981	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs35131119	chr15:56678982-56678983	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs551258883	chr15:56679036-56679037	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs552373044	chr15:56679059-56679060	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:61)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Testicular germ cell tumor	18059402	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
Colorectal cancer	16774939	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
Intellectual disability	22102821	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	CNVD
Prostate cancer	16573809	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Multiple myeloma	20724749	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Basal cell lymphoma	17053054	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Cancer	21129771	CNVD
Breast cancer	16272173	CNVD
Hepatocellular carcinoma	16750200	CNVD
Abnormal phenotypes	18644119	CNVD
Cancer	16751803	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Acute monocytic leukemia	16498392	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Breast cancer	17133270	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Gastric adenocarcinoma	19115996	CNVD
Congenital diaphragmatic hernia	21341218	CNVD
Holoprosencephaly	21359414	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Glioblastoma multiforme	21510904	CNVD

Chromatin state (count:1125 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:56664400-56685200	Weak transcription	Duodenum Mucosa	Duodenum
2	chr15:56665200-56733400	Weak transcription	Fetal Kidney	kidney
3	chr15:56672000-56694600	Weak transcription	Ovary	ovary
4	chr15:56673000-56678000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
5	chr15:56675000-56685000	Weak transcription	Fetal Intestine Small	intestine
6	chr15:56675400-56678600	Weak transcription	Thymus	Thymus
7	chr15:56675400-56691000	Weak transcription	Fetal Stomach	stomach
8	chr15:56676400-56678600	ZNF genes & repeats	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr15:56676400-56687400	Weak transcription	A549	lung
10	chr15:56676600-56678800	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr15:56676800-56677800	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
12	chr15:56676800-56678800	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr15:56677200-56691800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
14	chr15:56677400-56677800	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr15:56677400-56678000	Weak transcription	Cortex derived primary cultured neurospheres	brain
16	chr15:56677600-56684200	Weak transcription	GM12878-XiMat	blood
17	chr15:56677600-56709600	Weak transcription	Fetal Lung	lung
18	chr15:56677800-56690800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
19	chr15:56677800-56726200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
20	chr15:56678000-56678600	ZNF genes & repeats	Cortex derived primary cultured neurospheres	brain
21	chr15:56678000-56678600	ZNF genes & repeats	Ganglion Eminence derived primary cultured neurospheres	brain
22	chr15:56678600-56687000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr15:56678600-56690000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
24	chr15:56678600-56691800	Weak transcription	Cortex derived primary cultured neurospheres	brain
25	chr15:56678800-56689800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr15:56684200-56684600	ZNF genes & repeats	GM12878-XiMat	blood
27	chr15:56684600-56686800	Weak transcription	GM12878-XiMat	blood
28	chr15:56685000-56685600	Enhancers	Small Intestine	intestine
29	chr15:56685000-56686200	Enhancers	Fetal Intestine Small	intestine
30	chr15:56685200-56686200	Enhancers	Duodenum Mucosa	Duodenum
31	chr15:56686000-56734600	Weak transcription	Duodenum Smooth Muscle	Duodenum
32	chr15:56686200-56691400	Weak transcription	Duodenum Mucosa	Duodenum
33	chr15:56686400-56689000	Weak transcription	HUES6 Cell Line	embryonic stem cell
34	chr15:56686600-56686800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
35	chr15:56686800-56691000	ZNF genes & repeats	GM12878-XiMat	blood
36	chr15:56687000-56687800	ZNF genes & repeats	H9 Derived Neuron Cultured Cells	ES cell derived
37	chr15:56687000-56687800	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
38	chr15:56687800-56690000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
39	chr15:56687800-56691400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
40	chr15:56689000-56689200	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
41	chr15:56689400-56695000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
42	chr15:56690000-56690400	ZNF genes & repeats	Ganglion Eminence derived primary cultured neurospheres	brain
43	chr15:56690000-56690800	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
44	chr15:56690000-56692400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
45	chr15:56690000-56717400	Weak transcription	Dnd41	blood
46	chr15:56690000-56737800	Weak transcription	Stomach Mucosa	stomach
47	chr15:56690400-56691800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
48	chr15:56690400-56692800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
49	chr15:56690800-56692000	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
50	chr15:56691000-56692200	Strong transcription	Fetal Stomach	stomach

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