Variant report

Variant	nsv8880
Chromosome Location	chr1:225656408-225687710
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:981)
CpG islands
(count:916)
Chromatin interactive
region (count:73)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:5)

(count:981 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:225662672-225662961	HepG2	liver:	n/a	n/a
2	ATF2	chr1:225662522-225663052	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF2	chr1:225678342-225678695	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr1:225662618-225663049	GM12878	blood:	n/a	n/a
5	ATF3	chr1:225662733-225662914	GM12878	blood:	n/a	n/a
6	ATF3	chr1:225662670-225662973	K562	blood:	n/a	n/a
7	ATF3	chr1:225662524-225663048	A549	lung:	n/a	n/a
8	ATF3	chr1:225662504-225663165	A549	lung:	n/a	n/a
9	ATF3	chr1:225662710-225662979	HepG2	liver:	n/a	n/a
10	ATF3	chr1:225668678-225668889	K562	blood:	n/a	n/a
11	ATF3	chr1:225662673-225662962	K562	blood:	n/a	n/a
12	ATF3	chr1:225662673-225663001	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr1:225668564-225668953	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr1:225662493-225662984	H1-hESC	embryonic stem cell:	n/a	n/a
15	BATF	chr1:225686288-225686483	GM12878	blood:	n/a	chr1:225686374-225686385
16	BATF	chr1:225664356-225664634	GM12878	blood:	n/a	n/a
17	BATF	chr1:225664360-225664601	GM12878	blood:	n/a	n/a
18	BCL3	chr1:225672714-225673679	A549	lung:	n/a	chr1:225672752-225672765 chr1:225672761-225672769
19	BCL3	chr1:225662472-225663091	A549	lung:	n/a	chr1:225662827-225662840
20	BHLHE40	chr1:225658456-225658583	K562	blood:	n/a	n/a
21	BHLHE40	chr1:225668528-225668877	GM12878	blood:	n/a	n/a
22	BHLHE40	chr1:225662623-225663196	HepG2	liver:	n/a	n/a
23	BHLHE40	chr1:225662559-225663023	GM12878	blood:	n/a	n/a
24	BHLHE40	chr1:225683837-225684158	K562	blood:	n/a	n/a
25	BHLHE40	chr1:225662649-225663031	K562	blood:	n/a	n/a
26	BRCA1	chr1:225662609-225662996	HepG2	liver:	n/a	n/a
27	BRCA1	chr1:225662620-225663259	Hela-S3	cervix:	n/a	n/a
28	BRCA1	chr1:225662638-225663039	H1-hESC	embryonic stem cell:	n/a	n/a
29	BRCA1	chr1:225665382-225665516	GM12878	blood:	n/a	n/a
30	BRCA1	chr1:225662670-225662878	GM12878	blood:	n/a	n/a
31	CBX3	chr1:225665580-225665925	K562	blood:	n/a	n/a
32	CBX3	chr1:225662445-225663109	K562	blood:	n/a	n/a
33	CCNT2	chr1:225662667-225663105	K562	blood:	n/a	n/a
34	CEBPB	chr1:225662532-225663057	Hela-S3	cervix:	n/a	n/a
35	CEBPB	chr1:225662472-225663003	GM12878	blood:	n/a	n/a
36	CEBPB	chr1:225662715-225662922	HepG2	liver:	n/a	n/a
37	CEBPB	chr1:225661856-225661858	K562	blood:	n/a	n/a
38	CEBPB	chr1:225662549-225662940	K562	blood:	n/a	n/a
39	CEBPB	chr1:225662568-225662957	H1-hESC	embryonic stem cell:	n/a	n/a
40	CEBPB	chr1:225664286-225664501	IMR90	lung:	n/a	n/a
41	CEBPB	chr1:225662526-225662947	HepG2	liver:	n/a	n/a
42	CEBPB	chr1:225662563-225662901	K562	blood:	n/a	n/a
43	CHD1	chr1:225662766-225662817	H1-hESC	embryonic stem cell:	n/a	n/a
44	CHD1	chr1:225662385-225663232	IMR90	lung:	n/a	n/a
45	CHD1	chr1:225662674-225663001	GM12878	blood:	n/a	n/a
46	CHD2	chr1:225662532-225663115	HepG2	liver:	n/a	n/a
47	CHD2	chr1:225662605-225663030	Hela-S3	cervix:	n/a	n/a
48	CHD2	chr1:225662687-225662994	K562	blood:	n/a	n/a
49	CHD2	chr1:225662691-225663049	H1-hESC	embryonic stem cell:	n/a	n/a
50	CHD2	chr1:225662651-225663039	GM12878	blood:	n/a	n/a

(count:916 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:225661446-225661496	AG04449	skin:	fetal
2	chr1:225661446-225661496	AG04449	skin:	fetal
3	chr1:225676425-225676475	ECC-1	luminal epithelium:	n/a
4	chr1:225671862-225671912	NB4	blood:	n/a
5	chr1:225665763-225665813	A549	lung:	n/a
6	chr1:225665763-225665813	GM19239	blood:	n/a
7	chr1:225658651-225658701	HMEC	breast:	n/a
8	chr1:225671432-225671482	HIPEpiC	eye:	n/a
9	chr1:225671432-225671482	SAEC	small airway:	n/a
10	chr1:225658745-225658795	SK-N-SH	brain:	n/a
11	chr1:225662606-225662656	NH-A	brain:	n/a
12	chr1:225662350-225662400	HRE	kidney:	n/a
13	chr1:225662606-225662656	AG04449	skin:	fetal
14	chr1:225671990-225672040	GM12891	blood:	n/a
15	chr1:225658745-225658795	HEK293	kidney:	embryo
16	chr1:225662606-225662656	HCT-116	colon:	n/a
17	chr1:225659296-225659346	AG04450	lung:	fetal
18	chr1:225662675-225662725	U87	brain:	n/a
19	chr1:225662606-225662656	HCM	heart:	n/a
20	chr1:225671862-225671912	AG09319	gingival:	n/a
21	chr1:225662766-225662816	NHBE	bronchial:	n/a
22	chr1:225663401-225663451	H1-hESC	embryonic stem cell:	embryo
23	chr1:225662606-225662656	CMK	blood:	n/a
24	chr1:225671432-225671482	HMEC	breast:	n/a
25	chr1:225671862-225671912	Hepatocyte	liver:	n/a
26	chr1:225662350-225662400	RPTEC	kidney:	n/a
27	chr1:225665763-225665813	T-47D	breast:	n/a
28	chr1:225662606-225662656	SK-N-MC	brain:	n/a
29	chr1:225665763-225665813	HRPEpiC	eye:	n/a
30	chr1:225662606-225662656	NT2-D1	testis:	n/a
31	chr1:225662350-225662400	GM12892	blood:	n/a
32	chr1:225661446-225661496	AG04450	lung:	fetal
33	chr1:225671904-225671954	HAEpiC	amniotic membrane:	n/a
34	chr1:225662350-225662400	GM19239	blood:	n/a
35	chr1:225658745-225658795	HNPCEpiC	eye:	n/a
36	chr1:225661446-225661496	HCF	heart:	n/a
37	chr1:225676425-225676475	MCF10A-Er-Src	breast:	n/a
38	chr1:225671904-225671954	HCT-116	colon:	n/a
39	chr1:225665763-225665813	HAEpiC	amniotic membrane:	n/a
40	chr1:225658651-225658701	Caco-2	colon:	n/a
41	chr1:225661446-225661496	HRPEpiC	eye:	n/a
42	chr1:225671904-225671954	T-47D	breast:	n/a
43	chr1:225665763-225665813	HRCEpiC	kidney:	n/a
44	chr1:225662675-225662725	ProgFib	skin:	n/a
45	chr1:225671432-225671482	LNCaP	prostate:	n/a
46	chr1:225659296-225659346	BE2_C	brain:	n/a
47	chr1:225658651-225658701	A549	lung:	n/a
48	chr1:225676425-225676475	ProgFib	skin:	n/a
49	chr1:225658745-225658795	HPAEpiC	pulmonary alveolar:	n/a
50	chr1:225662606-225662656	Caco-2	colon:	n/a

(count:73 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr1:225662226..225663837-chr1:226162713..226165257,2	K562	blood:
2	chr1:225652545..225654089-chr1:225665937..225667726,2	K562	blood:
3	chr1:225649550..225651644-chr1:225657315..225659303,2	MCF-7	breast:
4	chr1:225668756..225671445-chr1:225674981..225676551,3	K562	blood:
5	chr1:225657432..225660259-chr1:225660834..225662970,2	K562	blood:
6	chr1:225662379..225663286-chr1:226163400..226164300,7	K562	blood:
7	chr1:225682780..225684982-chr1:225687181..225690046,2	MCF-7	breast:
8	chr1:225662355..225663302-chr1:225959684..225960794,13	K562	blood:
9	chr1:225662326..225663674-chr1:226098265..226099949,10	MCF-7	breast:
10	chr1:225667880..225669928-chr1:225980112..225982880,2	K562	blood:
11	chr1:225660270..225662835-chr1:225667398..225670221,2	MCF-7	breast:
12	chr1:225662375..225662892-chr1:226154381..226155127,2	K562	blood:
13	chr1:225662710..225663336-chr1:226154888..226155470,2	MCF-7	breast:
14	chr1:225660270..225662835-chr1:225667398..225670221,2	MCF-7	breast:
15	chr1:225602154..225602733-chr1:225662665..225663257,2	K562	blood:
16	chr1:225668021..225670369-chr1:226148124..226150238,2	MCF-7	breast:
17	chr1:225662353..225663278-chr1:226308878..226309804,6	K562	blood:
18	chr1:225674280..225677221-chr1:225997663..226000316,2	MCF-7	breast:
19	chr1:225662644..225663293-chr1:226308870..226309402,2	MCF-7	breast:
20	chr1:225662457..225663199-chr1:225705258..225705789,2	MCF-7	breast:
21	chr1:225668756..225671445-chr1:225674981..225676551,3	K562	blood:
22	chr1:225662700..225663253-chr1:226040369..226040954,2	MCF-7	breast:
23	chr1:225615551..225616246-chr1:225662296..225663262,2	MCF-7	breast:
24	chr1:225667455..225673405-chr1:225674170..225678275,6	MCF-7	breast:
25	chr1:225662449..225663280-chr1:226160613..226161497,3	K562	blood:
26	chr1:225625683..225626268-chr1:225662425..225662953,2	MCF-7	breast:
27	chr1:225668364..225669220-chr1:226309046..226309674,2	MCF-7	breast:
28	chr1:225662368..225663228-chr1:226027050..226027785,2	K562	blood:
29	chr1:225662701..225663242-chr1:226175273..226175841,2	MCF-7	breast:
30	chr1:225662349..225663258-chr1:225740687..225742425,6	K562	blood:
31	chr1:225662357..225662998-chr1:225754575..225755137,2	K562	blood:
32	chr1:225684757..225686780-chr1:225840497..225842307,2	MCF-7	breast:
33	chr1:225646024..225648970-chr1:225656905..225658780,2	K562	blood:
34	chr1:225667455..225673405-chr1:225674170..225678275,6	MCF-7	breast:
35	chr1:225662471..225663286-chr1:225959783..225960696,4	MCF-7	breast:
36	chr1:225662674..225663260-chr1:226156064..226156695,2	MCF-7	breast:
37	chr1:225662416..225663048-chr1:226150174..226150762,3	MCF-7	breast:
38	chr1:225662561..225663268-chr1:225685078..225685619,2	K562	blood:
39	chr1:225662400..225663321-chr1:225843274..225843784,2	K562	blood:
40	chr1:225662577..225663310-chr1:226384412..226385341,3	K562	blood:
41	chr1:225662303..225663219-chr1:226174962..226175679,3	MCF-7	breast:
42	chr1:225674187..225676643-chr1:225684973..225688505,3	K562	blood:
43	chr1:225631906..225634098-chr1:225666664..225668819,2	K562	blood:
44	chr1:225668772..225671386-chr1:225671515..225673412,2	K562	blood:
45	chr1:225668772..225671386-chr1:225671515..225673412,2	K562	blood:
46	chr1:225664480..225667161-chr1:225903900..225905865,2	K562	blood:
47	chr1:225660989..225663497-chr1:226070471..226072090,2	K562	blood:
48	chr1:225662607..225663273-chr1:225994915..225995627,2	K562	blood:
49	chr1:225662402..225663343-chr1:226032820..226034152,12	MCF-7	breast:
50	chr1:225655109..225657230-chr1:226022691..226024869,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC092811.1-1	chr1:225657547-225659222	XLOC_000585
2	lnc-AC092811.1-1	chr1:225659565-225660157	XLOC_000585

No data

(count:5 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	ENAH	hsa-miR-124-3p	chr1:225674888-225674882
2	ENAH	hsa-miR-181a-5p	chr1:225682791-225682784
3	ENAH	hsa-miR-124-3p	chr1:225683220-225683214
4	ENAH	hsa-miR-375	chr1:225684946-225684940
5	ENAH	hsa-miR-181a-5p	chr1:225682671-225682665

Variant related genes	Relation type
ENSG00000234476	TF binding region
ENSG00000234476	CpG island
ENSG00000196187	chromatin interactions
ENSG00000143811	chromatin interactions
ENSG00000143815	chromatin interactions
ENSG00000154380	chromatin interactions
ENSG00000242861	chromatin interactions
ENSG00000143819	chromatin interactions
ENSG00000143742	chromatin interactions
ENSG00000243709	chromatin interactions
ENSG00000234476	chromatin interactions
ARL8B	miRNA target sites

Extended variants
information (count: 1207 )
Associated
traits (count: 89 )

Variant overlapped rSNPs/rCNVs (count:1207 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs527990731	chr1:225656414-225656415	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs111230984	chr1:225656433-225656434	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs182674866	chr1:225656543-225656544	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs3856157	chr1:225656627-225656628	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs549630984	chr1:225656655-225656656	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs571296993	chr1:225656715-225656716	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs187326120	chr1:225656764-225656765	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs532812446	chr1:225656765-225656766	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs35639542	chr1:225656858-225656859	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs142159294	chr1:225656869-225656870	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs553538344	chr1:225656887-225656888	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs3893033	chr1:225656892-225656893	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs536142381	chr1:225656941-225656942	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs373818252	chr1:225656995-225656996	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs35830584	chr1:225657002-225657003	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs367980180	chr1:225657018-225657019	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs550391111	chr1:225657044-225657045	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs566454155	chr1:225657048-225657049	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs554400914	chr1:225657051-225657052	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs569019659	chr1:225657183-225657184	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs192569385	chr1:225657277-225657278	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs544574501	chr1:225657281-225657282	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs562875719	chr1:225657391-225657392	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs184373014	chr1:225657408-225657409	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs140993870	chr1:225657416-225657417	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs560674173	chr1:225657440-225657441	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs188931166	chr1:225657541-225657542	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs193111897	chr1:225657554-225657555	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
29	rs561534463	chr1:225657570-225657571	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
30	rs531234492	chr1:225657584-225657585	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
31	rs549732166	chr1:225657633-225657634	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
32	rs184813158	chr1:225657656-225657657	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
33	rs113055524	chr1:225657692-225657693	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
34	rs188846129	chr1:225657710-225657711	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
35	rs554842952	chr1:225657786-225657787	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
36	rs181690849	chr1:225657794-225657795	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
37	rs4554690	chr1:225657798-225657799	Weak transcription Enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs111927642	chr1:225657811-225657812	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
39	rs183950262	chr1:225657839-225657840	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
40	rs537894053	chr1:225657858-225657859	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
41	rs556519266	chr1:225657861-225657862	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
42	rs189607212	chr1:225657869-225657870	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
43	rs116315054	chr1:225657870-225657871	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
44	rs554276958	chr1:225657894-225657895	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
45	rs572702280	chr1:225657914-225657915	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
46	rs543218693	chr1:225657915-225657916	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
47	rs561454203	chr1:225657918-225657919	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
48	rs568705478	chr1:225657930-225657931	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
49	rs150301565	chr1:225657960-225657961	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
50	rs371297396	chr1:225657961-225657962	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a

Variant related diseases (count:89)

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
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
Glioblastoma multiforme	21138945	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Cancer	20164920	CNVD
Cancer	17060936	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:857 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:225649800-225662600	Weak transcription	Pancreas	Pancrea
2	chr1:225651400-225662400	Weak transcription	Fetal Brain Male	brain
3	chr1:225653600-225662400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr1:225653600-225662400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr1:225653800-225659600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
6	chr1:225654600-225656600	Enhancers	Lung	lung
7	chr1:225655400-225662400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
8	chr1:225655600-225658800	Weak transcription	HUES6 Cell Line	embryonic stem cell
9	chr1:225655600-225677000	Weak transcription	Right Atrium	heart
10	chr1:225655800-225656600	Enhancers	Colon Smooth Muscle	Colon
11	chr1:225655800-225658000	Enhancers	Fetal Muscle Trunk	muscle
12	chr1:225655800-225658000	Weak transcription	Skeletal Muscle Female	skeletal muscle
13	chr1:225655800-225658600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr1:225655800-225661200	Weak transcription	Brain Hippocampus Middle	brain
15	chr1:225655800-225661800	Weak transcription	Spleen	Spleen
16	chr1:225655800-225662000	Weak transcription	Right Ventricle	heart
17	chr1:225656000-225656600	Enhancers	Primary hematopoietic stem cells short term culture	blood
18	chr1:225656000-225656600	Flanking Active TSS	Primary T helper memory cells from peripheral blood 2	blood
19	chr1:225656000-225656800	Enhancers	Primary monocytes fromperipheralblood	blood
20	chr1:225656000-225657000	Enhancers	Primary B cells from cord blood	blood
21	chr1:225656000-225659200	Enhancers	Fetal Muscle Leg	muscle
22	chr1:225656200-225656600	Enhancers	Primary neutrophils fromperipheralblood	blood
23	chr1:225656200-225656800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
24	chr1:225656200-225656800	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
25	chr1:225656200-225657000	Enhancers	Rectal Mucosa Donor 29	rectum
26	chr1:225656200-225657200	Enhancers	Primary B cells from peripheral blood	blood
27	chr1:225656200-225657200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
28	chr1:225656200-225657200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
29	chr1:225656200-225659800	Enhancers	Stomach Smooth Muscle	stomach
30	chr1:225656400-225656600	Enhancers	GM12878-XiMat	blood
31	chr1:225656400-225656800	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
32	chr1:225656400-225656800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
33	chr1:225656400-225656800	Enhancers	Monocytes-CD14+_RO01746	blood
34	chr1:225656400-225657000	Enhancers	Primary T cells from cord blood	blood
35	chr1:225656400-225657000	Enhancers	Primary T killer memory cells from peripheral blood	blood
36	chr1:225656400-225657200	Enhancers	Primary T cells fromperipheralblood	blood
37	chr1:225656400-225657200	Enhancers	Primary T helper naive cells from peripheral blood	blood
38	chr1:225656400-225657200	Enhancers	Primary T helper cells PMA-I stimulated	--
39	chr1:225656400-225657400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
40	chr1:225656400-225657400	Enhancers	Primary T helper cells fromperipheralblood	blood
41	chr1:225656400-225657400	Enhancers	Primary T regulatory cells fromperipheralblood	blood
42	chr1:225656400-225657400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
43	chr1:225656400-225657800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
44	chr1:225656400-225658000	Weak transcription	Rectal Smooth Muscle	rectum
45	chr1:225656400-225658000	Weak transcription	Skeletal Muscle Male	skeletal muscle
46	chr1:225656400-225660000	Enhancers	Fetal Thymus	thymus
47	chr1:225656400-225662400	Weak transcription	Liver	Liver
48	chr1:225656400-225662600	Weak transcription	Thymus	Thymus
49	chr1:225656600-225657200	Weak transcription	Colon Smooth Muscle	Colon
50	chr1:225656600-225657600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood

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