Variant report

Variant	esv2761865
Chromosome Location	chr15:35101678-35271639
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1817)
CpG islands
(count:1221)
Chromatin interactive
region (count:99)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1817 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:35212450-35212797	K562	blood:	n/a	n/a
2	ARID3A	chr15:35261803-35262262	HepG2	liver:	n/a	n/a
3	ARID3A	chr15:35264405-35264692	K562	blood:	n/a	n/a
4	ARID3A	chr15:35110394-35110528	K562	blood:	n/a	n/a
5	ARID3A	chr15:35196884-35197044	K562	blood:	n/a	n/a
6	ARID3A	chr15:35184857-35184898	K562	blood:	n/a	n/a
7	ARID3A	chr15:35261871-35262154	K562	blood:	n/a	n/a
8	ARID3A	chr15:35109701-35109843	K562	blood:	n/a	n/a
9	ATF1	chr15:35118846-35118999	K562	blood:	n/a	n/a
10	ATF1	chr15:35265807-35266010	K562	blood:	n/a	n/a
11	ATF1	chr15:35196859-35197041	K562	blood:	n/a	n/a
12	ATF1	chr15:35120936-35121253	K562	blood:	n/a	n/a
13	ATF1	chr15:35171354-35171720	K562	blood:	n/a	n/a
14	ATF1	chr15:35261742-35262218	K562	blood:	n/a	n/a
15	ATF2	chr15:35261612-35262272	GM12878	blood:	n/a	n/a
16	ATF2	chr15:35261677-35262277	GM12878	blood:	n/a	n/a
17	ATF2	chr15:35261671-35262213	H1-hESC	embryonic stem cell:	n/a	n/a
18	ATF2	chr15:35261731-35262303	H1-hESC	embryonic stem cell:	n/a	n/a
19	ATF3	chr15:35261620-35262311	A549	lung:	n/a	n/a
20	ATF3	chr15:35261387-35262348	A549	lung:	n/a	n/a
21	ATF3	chr15:35261752-35262249	K562	blood:	n/a	n/a
22	BACH1	chr15:35261607-35262299	H1-hESC	embryonic stem cell:	n/a	n/a
23	BACH1	chr15:35196895-35197060	K562	blood:	n/a	n/a
24	BACH1	chr15:35145678-35145897	H1-hESC	embryonic stem cell:	n/a	n/a
25	BATF	chr15:35261808-35262220	GM12878	blood:	n/a	n/a
26	BATF	chr15:35245966-35246207	GM12878	blood:	n/a	chr15:35246068-35246079
27	BCL11A	chr15:35261796-35262190	GM12878	blood:	n/a	chr15:35262019-35262028
28	BCL3	chr15:35261589-35262356	A549	lung:	n/a	chr15:35262019-35262028
29	BCL3	chr15:35261592-35262356	A549	lung:	n/a	chr15:35262019-35262028
30	BCLAF1	chr15:35261727-35262206	K562	blood:	n/a	chr15:35262019-35262028
31	BCLAF1	chr15:35261580-35262273	GM12878	blood:	n/a	chr15:35262019-35262028
32	BCLAF1	chr15:35261666-35262306	GM12878	blood:	n/a	chr15:35262019-35262028
33	BCLAF1	chr15:35261646-35262211	K562	blood:	n/a	chr15:35262019-35262028
34	BHLHE40	chr15:35212513-35212769	GM12878	blood:	n/a	n/a
35	BHLHE40	chr15:35142442-35142677	K562	blood:	n/a	n/a
36	BHLHE40	chr15:35129508-35129712	K562	blood:	n/a	n/a
37	BHLHE40	chr15:35117104-35117539	K562	blood:	n/a	n/a
38	BHLHE40	chr15:35261675-35262246	GM12878	blood:	n/a	n/a
39	BHLHE40	chr15:35261668-35262277	K562	blood:	n/a	n/a
40	BRCA1	chr15:35261766-35262148	GM12878	blood:	n/a	n/a
41	BRCA1	chr15:35102631-35103313	Hela-S3	cervix:	n/a	n/a
42	BRCA1	chr15:35261803-35262239	H1-hESC	embryonic stem cell:	n/a	n/a
43	BRCA1	chr15:35147527-35148169	Hela-S3	cervix:	n/a	n/a
44	BRCA1	chr15:35261733-35262293	Hela-S3	cervix:	n/a	n/a
45	BRCA1	chr15:35133067-35133098	Hela-S3	cervix:	n/a	n/a
46	BRCA1	chr15:35261775-35262147	HepG2	liver:	n/a	n/a
47	BRCA1	chr15:35212474-35212765	H1-hESC	embryonic stem cell:	n/a	n/a
48	CBX3	chr15:35261595-35262212	K562	blood:	n/a	n/a
49	CBX3	chr15:35185150-35185569	K562	blood:	n/a	n/a
50	CBX3	chr15:35261651-35262362	HCT-116	colon:	n/a	n/a

(count:1221 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:35238599-35238649	Hepatocyte	liver:	n/a
2	chr15:35238599-35238649	Hepatocyte	liver:	n/a
3	chr15:35147320-35147370	HRPEpiC	eye:	n/a
4	chr15:35111036-35111086	Caco-2	colon:	n/a
5	chr15:35262037-35262087	NB4	blood:	n/a
6	chr15:35262789-35262839	HUVEC	blood vessel:	n/a
7	chr15:35261906-35261956	H1-hESC	embryonic stem cell:	embryo
8	chr15:35147320-35147370	PFSK-1	brain:	n/a
9	chr15:35111036-35111086	HepG2	liver:	n/a
10	chr15:35262037-35262087	PFSK-1	brain:	n/a
11	chr15:35262785-35262835	SK-N-SH_RA	brain:	n/a
12	chr15:35262037-35262087	HEEpiC	esophagus:	n/a
13	chr15:35259506-35259556	NHBE	bronchial:	n/a
14	chr15:35111036-35111086	HPAEpiC	pulmonary alveolar:	n/a
15	chr15:35147320-35147370	Hela-S3	cervix:	n/a
16	chr15:35262084-35262134	ECC-1	luminal epithelium:	n/a
17	chr15:35111036-35111086	HRPEpiC	eye:	n/a
18	chr15:35178803-35178853	ProgFib	skin:	n/a
19	chr15:35262054-35262104	PrEC	prostate:	n/a
20	chr15:35202392-35202442	GM12891	blood:	n/a
21	chr15:35261855-35261905	BJ	skin:	n/a
22	chr15:35262037-35262087	Hela-S3	cervix:	n/a
23	chr15:35262789-35262839	RPTEC	kidney:	n/a
24	chr15:35262037-35262087	NH-A	brain:	n/a
25	chr15:35148637-35148687	HPAEpiC	pulmonary alveolar:	n/a
26	chr15:35261784-35261834	NHBE	bronchial:	n/a
27	chr15:35129641-35129691	T-47D	breast:	n/a
28	chr15:35262037-35262087	HPAEpiC	pulmonary alveolar:	n/a
29	chr15:35259506-35259556	GM12891	blood:	n/a
30	chr15:35261784-35261834	SK-N-MC	brain:	n/a
31	chr15:35261587-35261637	HRE	kidney:	n/a
32	chr15:35261784-35261834	GM06990	blood:	n/a
33	chr15:35259506-35259556	GM06990	blood:	n/a
34	chr15:35261855-35261905	GM12878	blood:	n/a
35	chr15:35178803-35178853	CMK	blood:	n/a
36	chr15:35262789-35262839	HCM	heart:	n/a
37	chr15:35103606-35103656	NHDF-neo	bronchial:	n/a
38	chr15:35178803-35178853	HepG2	liver:	n/a
39	chr15:35111036-35111086	AG04450	lung:	fetal
40	chr15:35259506-35259556	Hela-S3	cervix:	n/a
41	chr15:35262037-35262087	BJ	skin:	n/a
42	chr15:35261906-35261956	GM06990	blood:	n/a
43	chr15:35103606-35103656	BE2_C	brain:	n/a
44	chr15:35262084-35262134	PANC-1	pancreas:	n/a
45	chr15:35264425-35264475	HEK293	kidney:	embryo
46	chr15:35262084-35262134	AG10803	skin:	n/a
47	chr15:35262084-35262134	SK-N-MC	brain:	n/a
48	chr15:35103606-35103656	SAEC	small airway:	n/a
49	chr15:35262785-35262835	AoSMC	blood vessel:	n/a
50	chr15:35111036-35111086	H1-hESC	embryonic stem cell:	embryo

(count:99 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr15:35139930..35141497-chr15:35142763..35145375,2	K562	blood:
2	chr15:35252626..35258121-chr15:35259367..35263228,9	K562	blood:
3	chr15:35169980..35173467-chr15:35175029..35177005,3	K562	blood:
4	chr15:35116724..35120020-chr15:35120075..35123945,4	K562	blood:
5	chr15:35271111..35273085-chr15:35278848..35280594,2	MCF-7	breast:
6	chr15:35195184..35198331-chr15:35198423..35200783,3	K562	blood:
7	chr13:52023403..52026177-chr15:35180246..35182636,2	MCF-7	breast:
8	chr11:61594734..61595282-chr15:35261416..35262282,2	NB4	blood:
9	chr15:35162821..35165306-chr15:35168208..35170309,3	K562	blood:
10	chr15:35261639..35264057-chr15:35280199..35283795,4	MCF-7	breast:
11	chr15:35252403..35254603-chr15:35260374..35262627,3	K562	blood:
12	chr15:35264656..35267660-chr15:35277567..35281665,3	K562	blood:
13	chr15:35187656..35189304-chr15:35193173..35195571,2	K562	blood:
14	chr15:35271322..35272882-chr15:35274387..35275895,2	MCF-7	breast:
15	chr15:35110279..35112223-chr15:35114145..35117464,3	K562	blood:
16	chr15:35130591..35132648-chr15:35139707..35142491,2	K562	blood:
17	chr15:34875842..34878722-chr15:35253845..35256501,2	K562	blood:
18	chr15:35252626..35258121-chr15:35259367..35263228,9	K562	blood:
19	chr15:35151497..35153844-chr15:35156867..35158791,2	K562	blood:
20	chr15:35258173..35260115-chr15:35260348..35263178,2	K562	blood:
21	chr15:35266094..35268727-chr15:35270510..35273519,3	MCF-7	breast:
22	chr15:35198651..35201621-chr15:35206696..35208281,2	K562	blood:
23	chr15:35260390..35261999-chr15:35270459..35271963,2	K562	blood:
24	chr15:35260390..35261999-chr15:35270459..35271963,2	K562	blood:
25	chr15:35189106..35191007-chr15:35202848..35205608,2	K562	blood:
26	chr15:35199285..35200789-chr15:35201669..35204219,2	K562	blood:
27	chr15:35270344..35273433-chr15:35279404..35282437,5	MCF-7	breast:
28	chr15:34953489..34955951-chr15:35181219..35183157,2	K562	blood:
29	chr15:35195184..35198331-chr15:35198423..35200783,3	K562	blood:
30	chr15:35268446..35269973-chr15:35278837..35281410,2	MCF-7	breast:
31	chr15:35189106..35191007-chr15:35202848..35205608,2	K562	blood:
32	chr15:35267358..35269882-chr15:35273203..35276166,3	K562	blood:
33	chr15:35159789..35161996-chr15:35162346..35164521,2	K562	blood:
34	chr15:35116724..35120020-chr15:35120075..35123945,4	K562	blood:
35	chr15:35251304..35254918-chr15:35255503..35258833,5	K562	blood:
36	chr15:35107630..35110469-chr15:35254911..35257321,2	K562	blood:
37	chr15:35169980..35172331-chr15:35175029..35176671,2	K562	blood:
38	chr15:35261372..35262043-chr15:35279881..35280440,2	MCF-7	breast:
39	chr15:35202607..35205491-chr15:35208140..35210817,2	K562	blood:
40	chr15:35261588..35262237-chr15:35280214..35280953,2	NB4	blood:
41	chr15:35250897..35253183-chr15:35255083..35256675,3	K562	blood:
42	chr15:35261505..35262096-chr15:35280433..35281003,2	Hela-S3	cervix:
43	chr15:35260390..35263299-chr15:35270062..35272008,3	K562	blood:
44	chr15:35219148..35220809-chr15:35259856..35261653,2	K562	blood:
45	chr15:35091621..35093914-chr15:35110145..35112659,2	K562	blood:
46	chr15:35162821..35165306-chr15:35168208..35170309,3	K562	blood:
47	chr15:35091969..35094940-chr15:35115211..35117056,2	K562	blood:
48	chr15:35260342..35263784-chr15:35278927..35282487,7	K562	blood:
49	chr15:35116799..35120020-chr15:35120075..35122439,3	K562	blood:
50	chr15:35219148..35220809-chr15:35259856..35261653,2	K562	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC114546.1-3	chr15:35102697-35105124	ENSG00000250007
2	lnc-ACTC1-1	chr15:35160323-35160538	expReg_chr15_1403_-
3	lnc-AC114546.1-7	chr15:35141428-35141868	NONHSAT041608
4	lnc-AC114546.1-8	chr15:35138274-35138484	NONHSAT041607

No data

Variant related genes	Relation type
ENSG00000212768	TF binding region
ENSG00000231409	TF binding region
AQR	TF binding region
ENSG00000259751	TF binding region
ENSG00000212768	CpG island
ENSG00000231409	CpG island
AQR	CpG island
ENSG00000259751	CpG island
ENSG00000198146	chromatin interactions
ENSG00000134824	chromatin interactions
ENSG00000021776	chromatin interactions
ENSG00000202077	chromatin interactions
ENSG00000159251	chromatin interactions
ENSG00000134146	chromatin interactions
ENSG00000228350	chromatin interactions
ENSG00000201699	chromatin interactions
ENSG00000102786	chromatin interactions
ENSG00000169857	chromatin interactions
ENSG00000215252	chromatin interactions
ENSG00000212768	chromatin interactions
ENSG00000259751	chromatin interactions
ENSG00000248079	chromatin interactions
CD2AP	miRNA target sites

Extended variants
information (count: 5952 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:5952 , 50 per page) page: 1 2 3 4 5 6 7 ... 120

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs551485377	chr15:35101698-35101699	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs143446899	chr15:35101701-35101702	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs537665780	chr15:35101724-35101725	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs1992105	chr15:35101732-35101733	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs147970119	chr15:35101744-35101745	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs189697879	chr15:35101760-35101761	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs181234131	chr15:35101795-35101796	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs373995579	chr15:35101904-35101905	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs557137477	chr15:35101943-35101944	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs142029604	chr15:35101978-35101979	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs574257922	chr15:35101985-35101986	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs545134211	chr15:35101994-35101995	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs557054619	chr15:35102020-35102021	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs575285414	chr15:35102044-35102045	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs116705113	chr15:35102048-35102049	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs528298629	chr15:35102066-35102067	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs147325028	chr15:35102102-35102103	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs529219386	chr15:35102114-35102115	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs541296089	chr15:35102118-35102119	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs559119556	chr15:35102121-35102122	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs11852345	chr15:35102203-35102204	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs186021777	chr15:35102267-35102268	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs569771971	chr15:35102328-35102329	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs575058296	chr15:35102345-35102346	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs529220187	chr15:35102394-35102395	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs530580950	chr15:35102397-35102398	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs549639605	chr15:35102479-35102480	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs189740522	chr15:35102483-35102484	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs7183018	chr15:35102566-35102567	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs7165734	chr15:35102625-35102626	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs545698667	chr15:35102643-35102644	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs539113000	chr15:35102657-35102658	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs538648366	chr15:35102662-35102663	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs370732734	chr15:35102725-35102726	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
35	rs7182728	chr15:35102741-35102742	Weak transcription Enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs6495716	chr15:35102755-35102756	Weak transcription Enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs536340536	chr15:35102761-35102762	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
38	rs371480247	chr15:35102772-35102773	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
39	rs676303	chr15:35102776-35102777	Weak transcription Enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs573764003	chr15:35102826-35102827	Enhancers Weak transcription Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
41	rs78285994	chr15:35102832-35102833	Enhancers Weak transcription Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
42	rs534125420	chr15:35102844-35102845	Enhancers Weak transcription Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
43	rs7181795	chr15:35102905-35102906	Enhancers Weak transcription Flanking Active TSS	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs577964662	chr15:35102936-35102937	Enhancers Weak transcription Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
45	rs7166311	chr15:35102940-35102941	Enhancers Weak transcription Flanking Active TSS	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs563264578	chr15:35102987-35102988	Enhancers Weak transcription Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
47	rs114765565	chr15:35103000-35103001	Enhancers Weak transcription Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
48	rs549080735	chr15:35103023-35103024	Enhancers Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
49	rs561360009	chr15:35103067-35103068	Enhancers Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
50	rs6495717	chr15:35103105-35103106	Enhancers Flanking Active TSS	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:70)

Disease	PMID	Source
HDAC8	0	CNVD
NIPBL	0	CNVD
RAD21	0	CNVD
SMC1A	0	CNVD
SMC3	0	CNVD
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Angelman syndrome	16183798	CNVD
Acute lymphoblastic leukemia	20067559	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
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Breast cancer	17133270	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
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21785460	CNVD
Abnormal corpus callosum	21572526	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Autism	19204725	CNVD
Schizophrenia	19204725	CNVD
Schizophrenia	19149910	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Legius syndrome	19443465	CNVD
Holoprosencephaly	21359414	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Cancer	17440070	CNVD
Basal cell lymphoma	17053054	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
lymphocytic leukemia	21291569	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Cancer	20164920	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:4459 , 50 per page) page: 1 2 3 4 5 6 7 ... 90

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:35096000-35102000	Weak transcription	HMEC	breast
2	chr15:35096000-35102600	Weak transcription	Fetal Muscle Leg	muscle
3	chr15:35096200-35103000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
4	chr15:35096400-35102200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr15:35097600-35102200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
6	chr15:35099000-35102200	Weak transcription	K562	blood
7	chr15:35100200-35102800	Enhancers	Hela-S3	cervix
8	chr15:35100400-35102000	Weak transcription	HSMM	muscle
9	chr15:35100400-35102200	Weak transcription	Skeletal Muscle Female	skeletal muscle
10	chr15:35100400-35102200	Weak transcription	NHLF	lung
11	chr15:35100400-35103000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr15:35100400-35103000	Weak transcription	Right Ventricle	heart
13	chr15:35100600-35102000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
14	chr15:35100600-35102800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
15	chr15:35100800-35102000	Weak transcription	Osteobl	bone
16	chr15:35100800-35108200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
17	chr15:35101000-35102000	Weak transcription	HSMMtube	muscle
18	chr15:35101400-35102200	Enhancers	Muscle Satellite Cultured Cells	--
19	chr15:35102000-35103600	Enhancers	HMEC	breast
20	chr15:35102000-35105600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
21	chr15:35102000-35105800	Enhancers	HSMMtube	muscle
22	chr15:35102000-35106400	Enhancers	HSMM	muscle
23	chr15:35102000-35106400	Enhancers	NHDF-Ad	bronchial
24	chr15:35102000-35106600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr15:35102000-35106600	Enhancers	Osteobl	bone
26	chr15:35102200-35102600	Flanking Active TSS	Muscle Satellite Cultured Cells	--
27	chr15:35102200-35103400	Enhancers	Skeletal Muscle Female	skeletal muscle
28	chr15:35102200-35103400	Enhancers	Stomach Smooth Muscle	stomach
29	chr15:35102200-35103400	Enhancers	K562	blood
30	chr15:35102200-35104000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
31	chr15:35102200-35104000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
32	chr15:35102200-35104000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
33	chr15:35102200-35104200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
34	chr15:35102200-35106200	Enhancers	NHLF	lung
35	chr15:35102200-35106400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
36	chr15:35102400-35103600	Enhancers	A549	lung
37	chr15:35102600-35103000	Enhancers	Muscle Satellite Cultured Cells	--
38	chr15:35102600-35103200	Enhancers	Fetal Heart	heart
39	chr15:35102600-35103800	Enhancers	Fetal Muscle Leg	muscle
40	chr15:35102800-35103200	Enhancers	ES-I3 Cell Line	embryonic stem cell
41	chr15:35102800-35103200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
42	chr15:35102800-35103400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
43	chr15:35102800-35103600	Flanking Active TSS	Hela-S3	cervix
44	chr15:35102800-35104000	Enhancers	Placenta	Placenta
45	chr15:35102800-35106400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
46	chr15:35103000-35103400	Flanking Active TSS	Muscle Satellite Cultured Cells	--
47	chr15:35103000-35103400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
48	chr15:35103000-35103400	Enhancers	Right Ventricle	heart
49	chr15:35103000-35103600	Enhancers	NH-A	brain
50	chr15:35103000-35104200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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