Variant report

Variant	esv3369957
Chromosome Location	chr1:158915589-159003393
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1442)
CpG islands
(count:734)
Chromatin interactive
region (count:23)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1442 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr1:158985296-158985598	K562	blood:	n/a	n/a
2	ATF1	chr1:158992212-158992362	K562	blood:	n/a	n/a
3	ATF1	chr1:158979683-158980159	K562	blood:	n/a	n/a
4	ATF2	chr1:158978470-158978975	GM12878	blood:	n/a	n/a
5	ATF2	chr1:158985128-158985741	GM12878	blood:	n/a	n/a
6	ATF2	chr1:158969408-158969884	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr1:158985129-158985827	GM12878	blood:	n/a	n/a
8	ATF3	chr1:158985327-158985513	K562	blood:	n/a	n/a
9	BACH1	chr1:159000829-159000930	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr1:158969462-158969881	H1-hESC	embryonic stem cell:	n/a	n/a
11	BATF	chr1:158966132-158966379	GM12878	blood:	n/a	n/a
12	BATF	chr1:158985273-158985601	GM12878	blood:	n/a	chr1:158985456-158985467
13	BATF	chr1:158966067-158966420	GM12878	blood:	n/a	n/a
14	BCL11A	chr1:158978607-158978914	GM12878	blood:	n/a	chr1:158978887-158978896
15	BCL11A	chr1:158966081-158966327	GM12878	blood:	n/a	n/a
16	BCLAF1	chr1:158968542-158968880	GM12878	blood:	n/a	n/a
17	BCLAF1	chr1:158979353-158980167	GM12878	blood:	n/a	chr1:158979355-158979364
18	BCLAF1	chr1:158966155-158966402	GM12878	blood:	n/a	n/a
19	BCLAF1	chr1:158979429-158980065	GM12878	blood:	n/a	n/a
20	BCLAF1	chr1:158985083-158985898	GM12878	blood:	n/a	n/a
21	BCLAF1	chr1:158985227-158985842	GM12878	blood:	n/a	n/a
22	BCLAF1	chr1:158978480-158978976	GM12878	blood:	n/a	chr1:158978887-158978896
23	BHLHE40	chr1:158985101-158985707	GM12878	blood:	n/a	n/a
24	BHLHE40	chr1:158968486-158968864	GM12878	blood:	n/a	n/a
25	BHLHE40	chr1:158979236-158980038	GM12878	blood:	n/a	n/a
26	BHLHE40	chr1:158978511-158978916	GM12878	blood:	n/a	n/a
27	BHLHE40	chr1:158966157-158966444	GM12878	blood:	n/a	n/a
28	BHLHE40	chr1:158985290-158985648	K562	blood:	n/a	n/a
29	BHLHE40	chr1:158921939-158922537	GM12878	blood:	n/a	chr1:158921997-158922013
30	BRCA1	chr1:158978674-158978735	GM12878	blood:	n/a	n/a
31	BRCA1	chr1:158979337-158980558	Hela-S3	cervix:	n/a	n/a
32	BRCA1	chr1:158969378-158971208	Hela-S3	cervix:	n/a	n/a
33	CBX3	chr1:158985214-158985605	K562	blood:	n/a	n/a
34	CBX3	chr1:158985291-158985578	K562	blood:	n/a	n/a
35	CBX3	chr1:158921842-158922138	K562	blood:	n/a	n/a
36	CCNT2	chr1:158979674-158980235	K562	blood:	n/a	n/a
37	CCNT2	chr1:158970050-158970250	K562	blood:	n/a	n/a
38	CEBPB	chr1:158969405-158969862	H1-hESC	embryonic stem cell:	n/a	chr1:158969611-158969623
39	CEBPB	chr1:158979563-158979997	K562	blood:	n/a	n/a
40	CEBPB	chr1:158937084-158937196	A549	lung:	n/a	chr1:158937104-158937115
41	CEBPB	chr1:158979605-158979996	K562	blood:	n/a	n/a
42	CEBPB	chr1:158979654-158979981	K562	blood:	n/a	n/a
43	CEBPB	chr1:158977593-158977889	K562	blood:	n/a	chr1:158977685-158977696 chr1:158977720-158977731
44	CEBPB	chr1:158985259-158985911	IMR90	lung:	n/a	chr1:158985893-158985905
45	CEBPB	chr1:158977646-158977828	H1-hESC	embryonic stem cell:	n/a	chr1:158977685-158977696 chr1:158977720-158977731
46	CEBPB	chr1:158979315-158980401	IMR90	lung:	n/a	n/a
47	CEBPB	chr1:158977574-158977911	A549	lung:	n/a	chr1:158977685-158977696 chr1:158977720-158977731
48	CEBPB	chr1:158985267-158985623	Hela-S3	cervix:	n/a	n/a
49	CEBPB	chr1:158969455-158970765	Hela-S3	cervix:	n/a	chr1:158969611-158969623
50	CEBPB	chr1:158977552-158977885	Hela-S3	cervix:	n/a	chr1:158977685-158977696 chr1:158977720-158977731

(count:734 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:158978468-158978518	Caco-2	colon:	n/a
2	chr1:158969712-158969762	AG09319	gingival:	n/a
3	chr1:158978468-158978518	Caco-2	colon:	n/a
4	chr1:158969712-158969762	AG09319	gingival:	n/a
5	chr1:158979841-158979891	RPTEC	kidney:	n/a
6	chr1:158969712-158969762	HCT-116	colon:	n/a
7	chr1:158922584-158922634	HEK293	kidney:	embryo
8	chr1:158978468-158978518	HUVEC	blood vessel:	n/a
9	chr1:158969712-158969762	SK-N-SH_RA	brain:	n/a
10	chr1:158979841-158979891	HCPEpiC	choroid plexus:	n/a
11	chr1:158978957-158979007	HAEpiC	amniotic membrane:	n/a
12	chr1:158978504-158978554	ovcar-3	ovarian:	n/a
13	chr1:158969712-158969762	HEEpiC	esophagus:	n/a
14	chr1:158978468-158978518	HMEC	breast:	n/a
15	chr1:158979647-158979697	SK-N-MC	brain:	n/a
16	chr1:158944784-158944834	PrEC	prostate:	n/a
17	chr1:158944784-158944834	AG09309	skin:	n/a
18	chr1:158969712-158969762	MCF-7	breast:	n/a
19	chr1:158978504-158978554	GM12891	blood:	n/a
20	chr1:158979810-158979860	AoSMC	blood vessel:	n/a
21	chr1:158979538-158979588	HCPEpiC	choroid plexus:	n/a
22	chr1:158978468-158978518	BJ	skin:	n/a
23	chr1:158979810-158979860	LNCaP	prostate:	n/a
24	chr1:158978957-158979007	SK-N-SH	brain:	n/a
25	chr1:158979647-158979697	AG09319	gingival:	n/a
26	chr1:158979538-158979588	GM19239	blood:	n/a
27	chr1:158969712-158969762	SK-N-MC	brain:	n/a
28	chr1:158969712-158969762	HMEC	breast:	n/a
29	chr1:158978468-158978518	Hepatocyte	liver:	n/a
30	chr1:158979841-158979891	HEEpiC	esophagus:	n/a
31	chr1:159001170-159001220	AG04450	lung:	fetal
32	chr1:158969712-158969762	NT2-D1	testis:	n/a
33	chr1:158944784-158944834	HPAEpiC	pulmonary alveolar:	n/a
34	chr1:159001170-159001220	T-47D	breast:	n/a
35	chr1:158978468-158978518	NH-A	brain:	n/a
36	chr1:158969712-158969762	T-47D	breast:	n/a
37	chr1:158922584-158922634	SAEC	small airway:	n/a
38	chr1:158922584-158922634	U87	brain:	n/a
39	chr1:159001170-159001220	GM12891	blood:	n/a
40	chr1:158979538-158979588	PFSK-1	brain:	n/a
41	chr1:158984321-158984371	IMR90	lung:	fetal
42	chr1:158979810-158979860	Hela-S3	cervix:	n/a
43	chr1:159001170-159001220	PrEC	prostate:	n/a
44	chr1:159001170-159001220	SKMC	muscle:	n/a
45	chr1:158922584-158922634	HCM	heart:	n/a
46	chr1:159001170-159001220	IMR90	lung:	fetal
47	chr1:158944784-158944834	AG10803	skin:	n/a
48	chr1:158978468-158978518	NHBE	bronchial:	n/a
49	chr1:158979538-158979588	GM12878	blood:	n/a
50	chr1:158978468-158978518	HIPEpiC	eye:	n/a

(count:23 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:158640177..158642154-chr1:158966970..158969167,2	K562	blood:
2	chr1:158763178..158764363-chr1:158967947..158968721,3	MCF-7	breast:
3	chr1:158970577..158973262-chr1:158975751..158977296,2	K562	blood:
4	chr1:158954353..158956986-chr1:158959866..158962393,2	K562	blood:
5	chr1:158900682..158902203-chr1:158976628..158979178,2	K562	blood:
6	chr1:158954353..158956986-chr1:158959866..158962635,3	K562	blood:
7	chr1:158944012..158946277-chr1:158956964..158958723,2	K562	blood:
8	chr1:158980102..158980980-chr7:91467247..91467748,2	Hela-S3	cervix:
9	chr1:158978448..158981430-chr1:159044743..159047016,2	K562	blood:
10	chr1:158944012..158946277-chr1:158956964..158958723,2	K562	blood:
11	chr1:158934253..158936901-chr1:158944231..158946210,2	K562	blood:
12	chr1:158968169..158968975-chr1:159041872..159042414,2	K562	blood:
13	chr1:158475878..158476640-chr1:158968361..158968916,3	MCF-7	breast:
14	chr1:158476296..158476820-chr1:158968188..158969128,2	K562	blood:
15	chr1:158979699..158980284-chr16:31191231..31192125,2	Hela-S3	cervix:
16	chr1:158970353..158971192-chr3:169482441..169483092,2	Hela-S3	cervix:
17	chr1:158934253..158936901-chr1:158944231..158946210,2	K562	blood:
18	chr1:158954353..158956986-chr1:158959866..158962393,2	K562	blood:
19	chr1:158954353..158956986-chr1:158959866..158962635,3	K562	blood:
20	chr1:158909146..158911653-chr1:158916474..158918051,2	K562	blood:
21	chr1:158647173..158649566-chr1:158944147..158946933,2	K562	blood:
22	chr1:158173526..158174221-chr1:158968084..158968716,3	MCF-7	breast:
23	chr1:158768206..158768907-chr1:158968540..158969106,3	MCF-7	breast:

No data

Variant related genes	Relation type
IFI16	TF binding region
IFI16	CpG island
ENSG00000089280	chromatin interactions
ENSG00000163568	chromatin interactions
ENSG00000270141	chromatin interactions
ENSG00000163565	chromatin interactions
ENSG00000176320	chromatin interactions
ENSG00000163564	chromatin interactions

Extended variants
information (count: 3616 )
Associated
traits (count: 109 )

Variant overlapped rSNPs/rCNVs (count:3616 , 50 per page) page: 1 2 3 4 5 6 7 ... 73

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs551909006	chr1:158915654-158915655	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs34388944	chr1:158915683-158915684	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs571450421	chr1:158915718-158915719	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs72704922	chr1:158915726-158915727	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs200201154	chr1:158915734-158915735	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs150393872	chr1:158915767-158915768	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs547565638	chr1:158915842-158915843	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs861319	chr1:158915917-158915918	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs117843190	chr1:158915922-158915923	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs533982902	chr1:158915958-158915959	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs190676952	chr1:158916055-158916056	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs856085	chr1:158916115-158916116	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs540379649	chr1:158916116-158916117	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs559979505	chr1:158916148-158916149	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs533517937	chr1:158916149-158916150	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs545292406	chr1:158916197-158916198	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs563971200	chr1:158916215-158916216	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs531141187	chr1:158916268-158916269	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs573932020	chr1:158916271-158916272	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs549335675	chr1:158916272-158916273	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs141378228	chr1:158916304-158916305	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs555879723	chr1:158916320-158916321	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs145557906	chr1:158916337-158916338	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs566831497	chr1:158916338-158916339	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs143806258	chr1:158916345-158916346	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs180689413	chr1:158916359-158916360	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs553757594	chr1:158916364-158916365	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs549102045	chr1:158916373-158916374	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs4053507	chr1:158916376-158916377	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs59771498	chr1:158916382-158916383	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs186143458	chr1:158916394-158916395	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs556894331	chr1:158916395-158916396	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs569119476	chr1:158916405-158916406	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs372940454	chr1:158916428-158916429	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs191114103	chr1:158916438-158916439	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs182775699	chr1:158916512-158916513	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs540246034	chr1:158916555-158916556	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs72704925	chr1:158916678-158916679	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs576877719	chr1:158916728-158916729	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs545566826	chr1:158916741-158916742	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs370312312	chr1:158916763-158916764	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs531231972	chr1:158916769-158916770	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs141376280	chr1:158916865-158916866	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs856086	chr1:158916918-158916919	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
45	rs139039188	chr1:158916970-158916971	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs578152824	chr1:158916978-158916979	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs528422517	chr1:158917037-158917038	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs538850638	chr1:158917042-158917043	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs546611199	chr1:158917073-158917074	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs571681208	chr1:158917123-158917124	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:109)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Liposarcoma	21253554	CNVD
Non-small cell lung cancer	21385341	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Cervical cancer	21062161	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	21183584	CNVD
Multiple myeloma	16461302	CNVD
Lung cancer	18438408	CNVD
Rett syndrome	21593744	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Systemic lupus erythematosus	21956041	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Non-small cell lung cancer	21829676	CNVD
Carcinoma ex pleomorphic adenoma	18828159	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
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	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
Neuroblastoma	21899760	CNVD
Breast cancer	17899364	CNVD
Bladder cancer	19088036	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Retinoblastoma	19183342	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Type 2 diabetes	19141583	CNVD
Chordoma	18071362	CNVD
Hepatocellular carcinoma	18803288	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Urothelial carcinoma	21177765	CNVD
Burkitt''s lymphoma	19759907	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21509527	CNVD
Bladder cancer	21909424	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Testicular germ cell tumor	18059402	CNVD
Trisomy 5 syndrome	21098271	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Breast cancer	21611746	CNVD
Neuroblastoma	18923191	CNVD
Systemic lupus erythematosus	19220326	CNVD
Systemic lupus erythematosus	19287148	CNVD
Glomerulonephritis	19341492	CNVD
Systemic lupus erythematosus	18559452	CNVD
Systemic autoimmune disease	17597778	CNVD
Glomerulonephritis	17008540	CNVD
Glomerulonephritis	16482158	CNVD
Soft tissue tumor	16732325	CNVD
Cancer	17060936	CNVD
Lung cancer	16740712	CNVD
Breast cancer	21045282	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Cancer	20164920	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Follicular lymphoma	18703704	CNVD
Pancreatic cancer	17952125	CNVD
Myelofibrosis	22110671	CNVD
Intracranial ependymoma	16609018	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:2234 , 50 per page) page: 1 2 3 4 5 6 7 ... 45

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:158902200-158920000	Weak transcription	Primary B cells from peripheral blood	blood
2	chr1:158905600-158921800	Strong transcription	Primary T cells fromperipheralblood	blood
3	chr1:158905600-158922000	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
4	chr1:158905800-158930200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
5	chr1:158906600-158919600	Strong transcription	Primary T helper cells fromperipheralblood	blood
6	chr1:158907000-158919200	Strong transcription	Primary T helper memory cells from peripheral blood 1	blood
7	chr1:158907200-158918200	Weak transcription	Primary B cells from cord blood	blood
8	chr1:158909200-158921800	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
9	chr1:158911000-158922400	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
10	chr1:158912800-158917600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr1:158913200-158922200	Strong transcription	Primary T cells from cord blood	blood
12	chr1:158913400-158922800	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
13	chr1:158913600-158922800	Strong transcription	Primary T helper cells PMA-I stimulated	--
14	chr1:158914600-158915600	Genic enhancers	Primary T helper naive cells from peripheral blood	blood
15	chr1:158914600-158916000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr1:158915200-158915600	Genic enhancers	Primary T helper memory cells from peripheral blood 2	blood
17	chr1:158915200-158916000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
18	chr1:158915200-158916600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
19	chr1:158915600-158917200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
20	chr1:158915600-158918800	Strong transcription	Primary T helper memory cells from peripheral blood 2	blood
21	chr1:158916000-158917400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr1:158916000-158920600	Strong transcription	Primary T killer memory cells from peripheral blood	blood
23	chr1:158916600-158917600	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
24	chr1:158917200-158922800	Strong transcription	Primary T helper naive cells from peripheral blood	blood
25	chr1:158917600-158919800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
26	chr1:158918200-158920200	Strong transcription	Primary B cells from cord blood	blood
27	chr1:158918400-158923400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
28	chr1:158918800-158919000	Genic enhancers	Primary T helper memory cells from peripheral blood 2	blood
29	chr1:158919000-158922000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
30	chr1:158919200-158922200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
31	chr1:158919600-158920000	ZNF genes & repeats	Primary T helper cells fromperipheralblood	blood
32	chr1:158919800-158920400	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
33	chr1:158919800-158922000	Weak transcription	Dnd41	blood
34	chr1:158920000-158921800	Enhancers	Primary B cells from peripheral blood	blood
35	chr1:158920000-158922200	Weak transcription	Duodenum Mucosa	Duodenum
36	chr1:158920000-158923000	Strong transcription	Primary T helper cells fromperipheralblood	blood
37	chr1:158920200-158921000	Weak transcription	Primary B cells from cord blood	blood
38	chr1:158920400-158921800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
39	chr1:158920600-158950600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
40	chr1:158921000-158922000	Enhancers	Primary B cells from cord blood	blood
41	chr1:158921600-158922200	Active TSS	GM12878-XiMat	blood
42	chr1:158921800-158922400	Flanking Active TSS	Primary B cells from peripheral blood	blood
43	chr1:158921800-158922800	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
44	chr1:158921800-158923000	Genic enhancers	Primary T cells fromperipheralblood	blood
45	chr1:158921800-158923000	Genic enhancers	Primary Natural Killer cells fromperipheralblood	blood
46	chr1:158922000-158922200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
47	chr1:158922000-158922200	Genic enhancers	Primary T regulatory cells fromperipheralblood	blood
48	chr1:158922000-158922400	Flanking Active TSS	Primary B cells from cord blood	blood
49	chr1:158922000-158922600	Enhancers	Primary hematopoietic stem cells short term culture	blood
50	chr1:158922200-158922400	Enhancers	ES-I3 Cell Line	embryonic stem cell

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