Variant report

Variant	esv2759001
Chromosome Location	chr1:225087924-225253274
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1209)
CpG islands
(count:549)
Chromatin interactive
region (count:72)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1209 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:225121406-225121573	K562	blood:	n/a	n/a
2	ARID3A	chr1:225117357-225117517	HepG2	liver:	n/a	n/a
3	ARID3A	chr1:225133723-225134019	HepG2	liver:	n/a	n/a
4	ARID3A	chr1:225169624-225170034	HepG2	liver:	n/a	n/a
5	ARID3A	chr1:225192292-225192433	HepG2	liver:	n/a	n/a
6	ATF1	chr1:225117186-225117593	K562	blood:	n/a	n/a
7	ATF1	chr1:225117958-225118374	K562	blood:	n/a	n/a
8	BACH1	chr1:225117256-225117761	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr1:225229451-225229466	K562	blood:	n/a	n/a
10	BCLAF1	chr1:225117146-225117805	K562	blood:	n/a	chr1:225117736-225117749 chr1:225117633-225117642 chr1:225117589-225117602
11	BCLAF1	chr1:225117128-225117697	K562	blood:	n/a	chr1:225117633-225117642 chr1:225117589-225117602
12	BHLHE40	chr1:225117111-225117835	K562	blood:	n/a	chr1:225117729-225117745 chr1:225117726-225117742 chr1:225117661-225117677
13	BHLHE40	chr1:225117300-225117534	GM12878	blood:	n/a	n/a
14	BRCA1	chr1:225117895-225118265	Hela-S3	cervix:	n/a	n/a
15	BRCA1	chr1:225117057-225117517	Hela-S3	cervix:	n/a	n/a
16	CBX3	chr1:225204354-225204636	K562	blood:	n/a	n/a
17	CBX3	chr1:225117860-225118566	K562	blood:	n/a	n/a
18	CBX3	chr1:225116923-225117782	HCT-116	colon:	n/a	n/a
19	CBX3	chr1:225116851-225117850	K562	blood:	n/a	n/a
20	CBX3	chr1:225119590-225120029	K562	blood:	n/a	n/a
21	CBX3	chr1:225251481-225251774	K562	blood:	n/a	n/a
22	CBX3	chr1:225121024-225122475	K562	blood:	n/a	n/a
23	CBX3	chr1:225120286-225120710	K562	blood:	n/a	n/a
24	CBX3	chr1:225101894-225102446	HCT-116	colon:	n/a	n/a
25	CBX3	chr1:225120283-225120696	K562	blood:	n/a	n/a
26	CBX3	chr1:225121107-225121821	K562	blood:	n/a	n/a
27	CBX3	chr1:225183306-225183672	HCT-116	colon:	n/a	n/a
28	CBX3	chr1:225117244-225117645	K562	blood:	n/a	n/a
29	CCNT2	chr1:225117187-225117853	K562	blood:	n/a	n/a
30	CEBPB	chr1:225133750-225134015	HepG2	liver:	n/a	n/a
31	CEBPB	chr1:225182674-225182786	H1-hESC	embryonic stem cell:	n/a	n/a
32	CEBPB	chr1:225232035-225232261	H1-hESC	embryonic stem cell:	n/a	chr1:225232161-225232172
33	CEBPB	chr1:225185883-225186203	ECC-1	luminal epithelium:	n/a	chr1:225186076-225186087
34	CEBPB	chr1:225133801-225133998	HepG2	liver:	n/a	n/a
35	CEBPB	chr1:225185938-225186201	A549	lung:	n/a	chr1:225186076-225186087
36	CEBPB	chr1:225185901-225186263	HepG2	liver:	n/a	chr1:225186076-225186087
37	CEBPB	chr1:225117078-225117548	Hela-S3	cervix:	n/a	n/a
38	CEBPB	chr1:225185929-225186321	A549	lung:	n/a	chr1:225186076-225186087
39	CEBPB	chr1:225133720-225134060	HepG2	liver:	n/a	n/a
40	CEBPB	chr1:225144265-225144303	A549	lung:	n/a	n/a
41	CEBPB	chr1:225232025-225232315	K562	blood:	n/a	chr1:225232161-225232172
42	CEBPB	chr1:225188410-225188431	HepG2	liver:	n/a	chr1:225188414-225188425
43	CEBPB	chr1:225214987-225215033	A549	lung:	n/a	n/a
44	CEBPB	chr1:225185911-225186272	K562	blood:	n/a	chr1:225186076-225186087
45	CEBPB	chr1:225182540-225182796	A549	lung:	n/a	n/a
46	CEBPB	chr1:225116949-225117427	K562	blood:	n/a	n/a
47	CEBPB	chr1:225232007-225232356	HepG2	liver:	n/a	chr1:225232161-225232172
48	CEBPB	chr1:225241393-225241550	HepG2	liver:	n/a	chr1:225241423-225241434 chr1:225241483-225241494
49	CEBPB	chr1:225185897-225186265	A549	lung:	n/a	chr1:225186076-225186087
50	CEBPB	chr1:225251396-225251573	HepG2	liver:	n/a	chr1:225251435-225251446

(count:549 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:225117464-225117514	SKMC	muscle:	n/a
2	chr1:225117464-225117514	K562	blood:	n/a
3	chr1:225117389-225117439	AG09309	skin:	n/a
4	chr1:225117750-225117800	U87	brain:	n/a
5	chr1:225116995-225117045	SK-N-MC	brain:	n/a
6	chr1:225117431-225117481	HRCEpiC	kidney:	n/a
7	chr1:225117431-225117481	HMEC	breast:	n/a
8	chr1:225117676-225117726	GM12878	blood:	n/a
9	chr1:225117389-225117439	HMEC	breast:	n/a
10	chr1:225116995-225117045	BJ	skin:	n/a
11	chr1:225117431-225117481	AG04449	skin:	fetal
12	chr1:225150341-225150391	AG09319	gingival:	n/a
13	chr1:225116995-225117045	SKMC	muscle:	n/a
14	chr1:225117431-225117481	HEEpiC	esophagus:	n/a
15	chr1:225117464-225117514	NT2-D1	testis:	n/a
16	chr1:225117076-225117126	RPTEC	kidney:	n/a
17	chr1:225117817-225117867	H1-hESC	embryonic stem cell:	embryo
18	chr1:225150341-225150391	ovcar-3	ovarian:	n/a
19	chr1:225116995-225117045	NB4	blood:	n/a
20	chr1:225117389-225117439	AG04449	skin:	fetal
21	chr1:225117676-225117726	ProgFib	skin:	n/a
22	chr1:225117750-225117800	MCF10A-Er-Src	breast:	n/a
23	chr1:225117389-225117439	Caco-2	colon:	n/a
24	chr1:225117676-225117726	Hela-S3	cervix:	n/a
25	chr1:225117431-225117481	Jurkat	blood:	n/a
26	chr1:225116995-225117045	PFSK-1	brain:	n/a
27	chr1:225117750-225117800	T-47D	breast:	n/a
28	chr1:225117750-225117800	BJ	skin:	n/a
29	chr1:225117464-225117514	HUVEC	blood vessel:	n/a
30	chr1:225116995-225117045	HAEpiC	amniotic membrane:	n/a
31	chr1:225117464-225117514	A549	lung:	n/a
32	chr1:225117464-225117514	AG09309	skin:	n/a
33	chr1:225117464-225117514	HEEpiC	esophagus:	n/a
34	chr1:225117817-225117867	HIPEpiC	eye:	n/a
35	chr1:225117676-225117726	AG04449	skin:	fetal
36	chr1:225117676-225117726	Jurkat	blood:	n/a
37	chr1:225117389-225117439	HAEpiC	amniotic membrane:	n/a
38	chr1:225117676-225117726	GM19239	blood:	n/a
39	chr1:225150341-225150391	HAEpiC	amniotic membrane:	n/a
40	chr1:225117389-225117439	NHBE	bronchial:	n/a
41	chr1:225116995-225117045	Caco-2	colon:	n/a
42	chr1:225117076-225117126	SKMC	muscle:	n/a
43	chr1:225117431-225117481	BE2_C	brain:	n/a
44	chr1:225117750-225117800	NT2-D1	testis:	n/a
45	chr1:225117076-225117126	LNCaP	prostate:	n/a
46	chr1:225117389-225117439	RPTEC	kidney:	n/a
47	chr1:225117464-225117514	AoSMC	blood vessel:	n/a
48	chr1:225117676-225117726	HCF	heart:	n/a
49	chr1:225117076-225117126	HRPEpiC	eye:	n/a
50	chr1:225117076-225117126	AG04449	skin:	fetal

(count:72 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr1:225229374..225230956-chr1:225231061..225233757,2	K562	blood:
2	chr1:224888777..224889662-chr1:225110350..225110931,2	K562	blood:
3	chr1:225187463..225189933-chr1:225191453..225195155,3	K562	blood:
4	chr1:225125254..225128428-chr1:225150698..225154229,3	K562	blood:
5	chr1:225125254..225128428-chr1:225150698..225154229,3	K562	blood:
6	chr1:8014073..8014650-chr1:225117304..225117825,2	Hela-S3	cervix:
7	chr1:225119003..225120746-chr1:225122614..225125497,2	MCF-7	breast:
8	chr1:225187463..225189933-chr1:225191453..225195155,3	K562	blood:
9	chr1:225122110..225123615-chr1:225123723..225125815,2	K562	blood:
10	chr1:225117129..225118085-chr13:31191178..31192009,2	NB4	blood:
11	chr1:225088133..225089884-chr1:225092314..225095237,2	K562	blood:
12	chr1:225118805..225120326-chr1:225154882..225156859,2	K562	blood:
13	chr1:225118656..225120791-chr1:225120817..225122470,2	K562	blood:
14	chr1:225146634..225148217-chr1:225149675..225151960,2	K562	blood:
15	chr1:225122110..225123615-chr1:225123723..225125815,2	K562	blood:
16	chr1:224832360..224832914-chr1:225110011..225110793,2	K562	blood:
17	chr1:225204703..225207335-chr1:225217608..225220449,2	K562	blood:
18	chr1:225119003..225120746-chr1:225122614..225125497,2	MCF-7	breast:
19	chr1:225229374..225230956-chr1:225231061..225233757,2	K562	blood:
20	chr1:225116699..225117668-chr3:73160108..73161088,2	Hela-S3	cervix:
21	chr1:225088133..225089884-chr1:225092314..225095237,2	K562	blood:
22	chr1:225116528..225119047-chr1:225122562..225124296,2	K562	blood:
23	chr1:225138712..225141214-chr1:225147432..225149142,2	MCF-7	breast:
24	chr1:225117101..225117940-chr2:9982915..9983806,2	Hela-S3	cervix:
25	chr1:153539179..153539769-chr1:225117355..225117966,2	Hela-S3	cervix:
26	chr1:225117903..225119549-chr1:225136065..225137999,2	K562	blood:
27	chr1:225040496..225041292-chr1:225109773..225110403,3	MCF-7	breast:
28	chr1:225066484..225067986-chr1:225113709..225116590,2	K562	blood:
29	chr1:225110317..225111909-chr1:225113611..225115449,2	K562	blood:
30	chr1:225117919..225119549-chr1:225136065..225138730,2	K562	blood:
31	chr1:225204703..225207335-chr1:225217608..225220449,2	K562	blood:
32	chr1:225117334..225118220-chr11:72524845..72525840,2	Hela-S3	cervix:
33	chr1:225135426..225138299-chr1:225142390..225144172,2	MCF-7	breast:
34	chr1:225119750..225122962-chr1:225123939..225127125,5	K562	blood:
35	chr1:225117194..225117809-chr12:113772563..113773224,2	NB4	blood:
36	chr1:225116223..225117951-chr1:225191253..225193259,2	MCF-7	breast:
37	chr1:225117903..225119549-chr1:225136065..225137999,2	K562	blood:
38	chr1:225226692..225229117-chr1:225229791..225231600,2	K562	blood:
39	chr1:224701183..224702131-chr1:225110304..225110969,3	MCF-7	breast:
40	chr1:225117301..225117958-chr5:140027420..140027937,2	Hela-S3	cervix:
41	chr1:225208646..225211614-chr1:225214288..225217124,2	K562	blood:
42	chr1:225118656..225120791-chr1:225120817..225122470,2	K562	blood:
43	chr1:225133403..225135871-chr1:225146349..225149223,2	K562	blood:
44	chr1:225117293..225117949-chr17:17184296..17185001,2	Hela-S3	cervix:
45	chr1:225146634..225148217-chr1:225149675..225151960,2	K562	blood:
46	chr1:225110059..225110580-chr14:54623098..54623598,2	MCF-7	breast:
47	chr1:225102785..225104962-chr1:225108843..225110479,2	K562	blood:
48	chr1:225112475..225114054-chr1:225116269..225117878,2	K562	blood:
49	chr1:225109346..225111069-chr1:225117045..225118611,2	MCF-7	breast:
50	chr1:225208646..225211614-chr1:225214288..225217124,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CNIH3-4	chr1:225155248-225155285	NONHSAT009831
2	lnc-CNIH3-4	chr1:225156461-225157195	NONHSAT009831

No data

Variant related genes	Relation type
DNAH14	TF binding region
DNAH14	CpG island
ENSG00000196754	chromatin interactions
ENSG00000223247	chromatin interactions
ENSG00000089060	chromatin interactions
ENSG00000143786	chromatin interactions
ENSG00000116288	chromatin interactions
ENSG00000264052	chromatin interactions
ENSG00000185842	chromatin interactions
ENSG00000168010	chromatin interactions
ENSG00000113141	chromatin interactions
ENSG00000189403	chromatin interactions
ENSG00000074319	chromatin interactions
ENSG00000141030	chromatin interactions
ENSG00000132952	chromatin interactions
ENSG00000115750	chromatin interactions

Extended variants
information (count: 5245 )
Associated
traits (count: 103 )

Variant overlapped rSNPs/rCNVs (count:5245 , 50 per page) page: 1 2 3 4 5 6 7 ... 105

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs115065508	chr1:225088406-225088407	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs569349895	chr1:225088420-225088421	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs540067965	chr1:225088421-225088422	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs559742095	chr1:225088427-225088428	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs567202270	chr1:225088434-225088435	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs112996681	chr1:225088452-225088453	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs111635991	chr1:225088468-225088469	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs374813684	chr1:225088479-225088480	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs182695340	chr1:225088520-225088521	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs555359126	chr1:225088539-225088540	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs573680653	chr1:225088541-225088542	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs188950171	chr1:225088542-225088543	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs35600674	chr1:225088587-225088588	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs150488721	chr1:225088614-225088615	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs370184302	chr1:225088629-225088630	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs572618656	chr1:225088638-225088639	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs192021733	chr1:225088650-225088651	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs548692564	chr1:225088691-225088692	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs545215557	chr1:225088741-225088742	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs183468874	chr1:225088761-225088762	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs568540138	chr1:225088825-225088826	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs112825645	chr1:225088842-225088843	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs542522635	chr1:225088843-225088844	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs2501099	chr1:225088856-225088857	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs529337511	chr1:225088951-225088952	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs550789351	chr1:225088973-225088974	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs80340527	chr1:225088997-225088998	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs187502071	chr1:225089015-225089016	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs192305906	chr1:225089042-225089043	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs567077015	chr1:225089052-225089053	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs534445498	chr1:225089069-225089070	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs2489340	chr1:225089075-225089076	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs567259598	chr1:225089090-225089091	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs537880522	chr1:225089153-225089154	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs555963680	chr1:225089161-225089162	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs184094660	chr1:225089227-225089228	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs187278970	chr1:225089240-225089241	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs138253049	chr1:225089241-225089242	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs571912907	chr1:225089266-225089267	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs577223776	chr1:225089273-225089274	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs114037814	chr1:225089280-225089281	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs560890525	chr1:225089288-225089289	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs142966434	chr1:225089341-225089342	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs146199281	chr1:225089355-225089356	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs373995223	chr1:225089356-225089357	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs533433580	chr1:225089431-225089432	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs137969517	chr1:225089441-225089442	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs560662256	chr1:225089444-225089445	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs142343606	chr1:225089459-225089460	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs527926903	chr1:225089467-225089468	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:103)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Autism	22495311	CNVD
Melanoma	18172304	CNVD
Rett syndrome	21593744	CNVD
Medulloblastoma	21979893	CNVD
Cancer	20164919	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Liposarcoma	21253554	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Breast cancer	17603634	CNVD
Neuroblastoma	21899760	CNVD
Breast cancer	21858162	CNVD
Non-small cell lung cancer	21385341	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Testicular germ cell tumor	18059402	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Breast cancer	21509527	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Chordoma	18071362	CNVD
T-cell lymphomas	19863542	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hepatocellular carcinoma	18803288	CNVD
Urothelial tumor	18831757	CNVD
Lung cancer	18438408	CNVD
Medulloblastoma	16783165	CNVD
Basal cell lymphoma	17170743	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Mental retardation	19951919	CNVD
Non-syndromic sensorineural hearing loss	17873649	CNVD
Basal cell lymphoma	17053054	CNVD
Developmental delay	21147756	CNVD
Autism	14699429	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Fumarase deficiency	21572526	CNVD
Autism	17483303	CNVD
Kartagener syndrome	16639409	CNVD
Congenital abnormalities	21549014	CNVD
Developmental delay	21549014	CNVD
Mental retardation	21549014	CNVD
small cell lung cancer	20016488	CNVD
Myelofibrosis	22110671	CNVD
Liver carcinoma	19366792	CNVD
Leukoplakia	24403051	CNVD
Congenital diaphragmatic hernia	21525063	CNVD
Glioblastoma multiforme	21138945	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Cancer	20164920	CNVD
Cancer	17060936	CNVD
Pancreatic cancer	17952125	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Alzheimer''s disease	22166940	CNVD
micrognathia	21364285	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:582 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:225088400-225090000	Enhancers	Fetal Thymus	thymus
2	chr1:225088600-225089800	Enhancers	Primary T cells from cord blood	blood
3	chr1:225090000-225091400	Weak transcription	Fetal Thymus	thymus
4	chr1:225091600-225091800	Enhancers	Fetal Thymus	thymus
5	chr1:225097800-225098600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr1:225098400-225098600	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr1:225098600-225102200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr1:225098800-225099200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr1:225099200-225099600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr1:225101600-225103800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr1:225102200-225102400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr1:225102400-225102800	Weak transcription	Pancreas	Pancrea
13	chr1:225102400-225110000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr1:225106800-225107000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr1:225106800-225107000	Enhancers	Liver	Liver
16	chr1:225106800-225107600	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
17	chr1:225106800-225107600	Active TSS	Duodenum Mucosa	Duodenum
18	chr1:225107000-225107200	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr1:225107000-225107400	Enhancers	Dnd41	blood
20	chr1:225107000-225107600	Flanking Active TSS	Liver	Liver
21	chr1:225107000-225107800	Enhancers	HepG2	liver
22	chr1:225107200-225107400	Enhancers	Small Intestine	intestine
23	chr1:225107200-225107600	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr1:225107400-225110000	Weak transcription	Dnd41	blood
25	chr1:225107600-225108000	Enhancers	Liver	Liver
26	chr1:225107600-225108800	Weak transcription	Duodenum Mucosa	Duodenum
27	chr1:225107600-225110000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr1:225108000-225109200	Weak transcription	Liver	Liver
29	chr1:225108400-225108600	Enhancers	Pancreas	Pancrea
30	chr1:225108600-225110000	Weak transcription	Pancreas	Pancrea
31	chr1:225108800-225109000	Enhancers	Duodenum Mucosa	Duodenum
32	chr1:225108800-225110200	Enhancers	Stomach Mucosa	stomach
33	chr1:225108800-225110400	Enhancers	Fetal Intestine Small	intestine
34	chr1:225109000-225109200	Enhancers	Gastric	stomach
35	chr1:225109000-225110400	Enhancers	Fetal Intestine Large	intestine
36	chr1:225109200-225109400	Enhancers	Liver	Liver
37	chr1:225109200-225110000	Weak transcription	Gastric	stomach
38	chr1:225109400-225109800	Weak transcription	Liver	Liver
39	chr1:225109800-225110800	Enhancers	Liver	Liver
40	chr1:225110000-225110200	Enhancers	Gastric	stomach
41	chr1:225110000-225110400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
42	chr1:225110000-225110400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
43	chr1:225110000-225110400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
44	chr1:225110000-225110400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
45	chr1:225110000-225110400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
46	chr1:225110000-225110400	Enhancers	Pancreas	Pancrea
47	chr1:225110000-225110400	Enhancers	Dnd41	blood
48	chr1:225110000-225111800	Enhancers	Ovary	ovary
49	chr1:225110200-225110400	Bivalent/Poised TSS	HepG2	liver
50	chr1:225110200-225110400	Bivalent Enhancer	K562	blood

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