Variant report

Variant	esv18420
Chromosome Location	chr1:149707658-149795271
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1434)
CpG islands
(count:1709)
Chromatin interactive
region (count:22)
LncRNA
region (count:12)
Mature miRNA
region (count: 0)
miRNA target
sites (count:4)

(count:1434 , 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	ARID3A	chr1:149748718-149748918	K562	blood:	n/a	n/a
2	ARID3A	chr1:149764085-149764195	K562	blood:	n/a	n/a
3	ARID3A	chr1:149764146-149764192	HepG2	liver:	n/a	n/a
4	ARID3A	chr1:149747121-149747405	K562	blood:	n/a	n/a
5	ARID3A	chr1:149783972-149784010	K562	blood:	n/a	n/a
6	ATF1	chr1:149785250-149785260	K562	blood:	n/a	n/a
7	ATF1	chr1:149783825-149784193	K562	blood:	n/a	n/a
8	ATF1	chr1:149747159-149747411	K562	blood:	n/a	n/a
9	ATF2	chr1:149783642-149784320	H1-hESC	embryonic stem cell:	n/a	n/a
10	ATF2	chr1:149784707-149784912	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF2	chr1:149783626-149784089	GM12878	blood:	n/a	n/a
12	ATF2	chr1:149783745-149784262	H1-hESC	embryonic stem cell:	n/a	n/a
13	ATF3	chr1:149711653-149712227	A549	lung:	n/a	n/a
14	ATF3	chr1:149711658-149712146	A549	lung:	n/a	n/a
15	ATF3	chr1:149759342-149759524	K562	blood:	n/a	n/a
16	ATF3	chr1:149783628-149783929	A549	lung:	n/a	n/a
17	BACH1	chr1:149783062-149783253	K562	blood:	n/a	n/a
18	BATF	chr1:149764009-149764293	GM12878	blood:	n/a	n/a
19	BATF	chr1:149711835-149712141	GM12878	blood:	n/a	chr1:149711949-149711958
20	BATF	chr1:149783540-149783843	GM12878	blood:	n/a	n/a
21	BATF	chr1:149743599-149744024	GM12878	blood:	n/a	n/a
22	BATF	chr1:149711785-149712234	GM12878	blood:	n/a	chr1:149711949-149711958
23	BATF	chr1:149783100-149783925	GM12878	blood:	n/a	n/a
24	BATF	chr1:149743595-149743947	GM12878	blood:	n/a	n/a
25	BATF	chr1:149784784-149785210	GM12878	blood:	n/a	n/a
26	BATF	chr1:149736086-149736381	GM12878	blood:	n/a	n/a
27	BATF	chr1:149784481-149784768	GM12878	blood:	n/a	n/a
28	BATF	chr1:149783127-149783478	GM12878	blood:	n/a	n/a
29	BATF	chr1:149764414-149764725	GM12878	blood:	n/a	n/a
30	BCL11A	chr1:149784375-149784762	GM12878	blood:	n/a	n/a
31	BCL11A	chr1:149764220-149764668	GM12878	blood:	n/a	n/a
32	BCL11A	chr1:149743550-149744000	GM12878	blood:	n/a	chr1:149743777-149743786 chr1:149743741-149743750
33	BCL11A	chr1:149743727-149744116	GM12878	blood:	n/a	chr1:149743777-149743786 chr1:149743741-149743750
34	BCL11A	chr1:149764379-149764550	GM12878	blood:	n/a	n/a
35	BCL11A	chr1:149783471-149783962	GM12878	blood:	n/a	n/a
36	BCL11A	chr1:149784900-149785289	GM12878	blood:	n/a	n/a
37	BCL11A	chr1:149784793-149785339	GM12878	blood:	n/a	n/a
38	BCL11A	chr1:149783133-149783977	GM12878	blood:	n/a	n/a
39	BCL3	chr1:149783632-149784100	A549	lung:	n/a	n/a
40	BCL3	chr1:149783609-149784438	A549	lung:	n/a	chr1:149784187-149784196 chr1:149784295-149784304
41	BCLAF1	chr1:149784581-149784922	K562	blood:	n/a	n/a
42	BCLAF1	chr1:149783628-149784428	K562	blood:	n/a	chr1:149784187-149784196 chr1:149784295-149784304
43	BCLAF1	chr1:149783669-149784321	K562	blood:	n/a	chr1:149784187-149784196 chr1:149784295-149784304
44	BCLAF1	chr1:149783745-149783991	GM12878	blood:	n/a	n/a
45	BCLAF1	chr1:149783624-149784080	GM12878	blood:	n/a	n/a
46	BCLAF1	chr1:149764461-149764768	GM12878	blood:	n/a	n/a
47	BHLHE40	chr1:149764585-149764716	GM12878	blood:	n/a	n/a
48	BHLHE40	chr1:149764016-149764210	HepG2	liver:	n/a	n/a
49	BHLHE40	chr1:149784098-149784190	GM12878	blood:	n/a	n/a
50	BHLHE40	chr1:149764150-149764212	GM12878	blood:	n/a	n/a

(count:1709 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:149764680-149764730	NHDF-neo	bronchial:	n/a
2	chr1:149764680-149764730	NHDF-neo	bronchial:	n/a
3	chr1:149758962-149759012	NB4	blood:	n/a
4	chr1:149784571-149784621	SKMC	muscle:	n/a
5	chr1:149717620-149717670	Hepatocyte	liver:	n/a
6	chr1:149784212-149784262	MCF10A-Er-Src	breast:	n/a
7	chr1:149785211-149785261	CMK	blood:	n/a
8	chr1:149784212-149784262	NB4	blood:	n/a
9	chr1:149783242-149783292	U87	brain:	n/a
10	chr1:149719461-149719511	NB4	blood:	n/a
11	chr1:149764294-149764344	GM06990	blood:	n/a
12	chr1:149721664-149721714	HNPCEpiC	eye:	n/a
13	chr1:149784212-149784262	SK-N-MC	brain:	n/a
14	chr1:149784212-149784262	HRCEpiC	kidney:	n/a
15	chr1:149784776-149784826	A549	lung:	n/a
16	chr1:149764680-149764730	Caco-2	colon:	n/a
17	chr1:149764739-149764789	RPTEC	kidney:	n/a
18	chr1:149764680-149764730	AG04449	skin:	fetal
19	chr1:149719536-149719586	PANC-1	pancreas:	n/a
20	chr1:149764342-149764392	MCF-7	breast:	n/a
21	chr1:149782411-149782461	AG09319	gingival:	n/a
22	chr1:149782411-149782461	HepG2	liver:	n/a
23	chr1:149753023-149753073	NHBE	bronchial:	n/a
24	chr1:149765026-149765076	HUVEC	blood vessel:	n/a
25	chr1:149764294-149764344	NHBE	bronchial:	n/a
26	chr1:149712057-149712107	GM12891	blood:	n/a
27	chr1:149764680-149764730	HCM	heart:	n/a
28	chr1:149784212-149784262	AG09319	gingival:	n/a
29	chr1:149764790-149764840	NB4	blood:	n/a
30	chr1:149764790-149764840	HCT-116	colon:	n/a
31	chr1:149719243-149719293	Hela-S3	cervix:	n/a
32	chr1:149764739-149764789	HRCEpiC	kidney:	n/a
33	chr1:149719536-149719586	PFSK-1	brain:	n/a
34	chr1:149783778-149783828	AG10803	skin:	n/a
35	chr1:149784851-149784901	BE2_C	brain:	n/a
36	chr1:149784851-149784901	U87	brain:	n/a
37	chr1:149785211-149785261	HCT-116	colon:	n/a
38	chr1:149767909-149767959	ECC-1	luminal epithelium:	n/a
39	chr1:149758962-149759012	AG09319	gingival:	n/a
40	chr1:149784212-149784262	HepG2	liver:	n/a
41	chr1:149784212-149784262	SK-N-SH	brain:	n/a
42	chr1:149784212-149784262	MCF-7	breast:	n/a
43	chr1:149721664-149721714	Jurkat	blood:	n/a
44	chr1:149784851-149784901	AG04449	skin:	fetal
45	chr1:149720577-149720627	HCPEpiC	choroid plexus:	n/a
46	chr1:149787666-149787716	HAEpiC	amniotic membrane:	n/a
47	chr1:149719536-149719586	ovcar-3	ovarian:	n/a
48	chr1:149717620-149717670	HMEC	breast:	n/a
49	chr1:149718651-149718701	BE2_C	brain:	n/a
50	chr1:149785211-149785261	AG09319	gingival:	n/a

(count:22 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:149780184..149786348-chr1:149813638..149819174,10	MCF-7	breast:
2	chr1:149764705..149766626-chr1:149783077..149785466,2	MCF-7	breast:
3	chr1:149783342..149785620-chr1:149887421..149889754,2	K562	blood:
4	chr1:149783798..149785644-chr1:149820070..149822937,2	MCF-7	breast:
5	chr1:146554326..146556624-chr1:149762818..149765682,2	K562	blood:
6	chr1:149783817..149784624-chr11:85780019..85780945,2	HCT-116	colon:
7	chr1:149782518..149784153-chr17:64298114..64300173,2	MCF-7	breast:
8	chr1:149780176..149782489-chr1:149856785..149858903,2	MCF-7	breast:
9	chr1:149758293..149760951-chr1:149816252..149817928,2	K562	blood:
10	chr1:144531697..144534436-chr1:149784086..149786783,2	K562	blood:
11	chr1:149782452..149784752-chr17:56707405..56709956,2	MCF-7	breast:
12	chr1:149783767..149785464-chr8:128748243..128750155,2	MCF-7	breast:
13	chr1:149776274..149778448-chr1:149782482..149785276,2	MCF-7	breast:
14	chr1:149780406..149781983-chr11:21191112..21193210,2	MCF-7	breast:
15	chr1:149790699..149793037-chr1:149857705..149860601,2	MCF-7	breast:
16	chr1:149783800..149785818-chr1:149904414..149906433,2	K562	blood:
17	chr1:149784782..149785302-chr18:33766792..33767490,2	Hela-S3	cervix:
18	chr1:149777219..149780233-chr1:149783761..149786780,3	K562	blood:
19	chr1:144532605..144534445-chr1:149782477..149783992,2	K562	blood:
20	chr1:149780176..149786781-chr1:149856138..149862217,21	MCF-7	breast:
21	chr1:149783982..149786331-chr20:46129581..46131527,2	MCF-7	breast:
22	chr1:24306115..24306820-chr1:149785025..149785525,2	Hela-S3	cervix:

(count:12 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-HIST2H4A-3	chr1:149754284-149754330	NONHSAT006247
2	lnc-FCGR1A-1	chr1:149771333-149771795	NONHSAT006251
3	lnc-HIST2H4A-3	chr1:149754726-149755507	NONHSAT006247
4	lnc-HIST2H2BF-3	chr1:149718450-149720133	NONHSAT006245
5	lnc-HIST2H2BF-3	chr1:149713129-149713281	NONHSAT006245
6	lnc-HIST2H4A-2	chr1:149762793-149763231	NONHSAT006250
7	lnc-HIST2H4A-2	chr1:149761924-149761961	NONHSAT006250
8	lnc-FCGR1A-1	chr1:149769027-149769076	NONHSAT006251
9	lnc-HIST2H3D-1	chr1:149757215-149759694	ENSG00000233030.2
10	lnc-HIST2H3D-2	chr1:149754433-149754816	ENSG00000242663.1
11	lnc-HIST2H3D-1	chr1:149763514-149764576	ENSG00000233030.2
12	lnc-HIST2H3D-2	chr1:149783238-149783312	ENSG00000242663.1

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location
1	HIST2H2BF	hsa-miR-125b-5p	chr1:149754502-149754527
2	HIST2H2BF	hsa-let-7a-5p	chr1:149754506-149754527
3	HIST2H2BF	hsa-miR-98-5p	chr1:149754506-149754531
4	HIST2H2BF	hsa-let-7e-5p	chr1:149754506-149754527

Variant related genes	Relation type
HIST2H2BF	TF binding region
ENSG00000234232	TF binding region
FCGR1A	TF binding region
HIST2H3D	TF binding region
ENSG00000263825	TF binding region
ENSG00000233030	TF binding region
ENSG00000242663	TF binding region
ENSG00000226500	TF binding region
HIST2H2BF	CpG island
ENSG00000234232	CpG island
FCGR1A	CpG island
HIST2H3D	CpG island
ENSG00000263825	CpG island
ENSG00000233030	CpG island
ENSG00000242663	CpG island
ENSG00000226500	CpG island
ENSG00000272993	chromatin interactions
ENSG00000261716	chromatin interactions
ENSG00000159164	chromatin interactions
ENSG00000124151	chromatin interactions
ENSG00000220323	chromatin interactions
ENSG00000201699	chromatin interactions
ENSG00000183598	chromatin interactions
ENSG00000184270	chromatin interactions
ENSG00000154229	chromatin interactions
ENSG00000075643	chromatin interactions
ENSG00000073921	chromatin interactions
ENSG00000184678	chromatin interactions
ENSG00000254816	chromatin interactions
ENSG00000203814	chromatin interactions
ENSG00000014914	chromatin interactions
ENSG00000183558	chromatin interactions
ENSG00000184260	chromatin interactions
ENSG00000212195	chromatin interactions
ENSG00000242663	chromatin interactions
ENSG00000178096	chromatin interactions
ENSG00000188529	chromatin interactions
ENSG00000136997	chromatin interactions
ENSG00000203812	chromatin interactions
ENSG00000230832	chromatin interactions
ENSG00000203819	chromatin interactions
ENSG00000260552	chromatin interactions

Extended variants
information (count: 2714 )
Associated
traits (count: 115 )

Variant overlapped rSNPs/rCNVs (count:2714 , 50 per page) page: 1 2 3 4 5 6 7 ... 55

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs587630152	chr1:149707701-149707702	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs587682962	chr1:149707726-149707727	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs114410627	chr1:149707742-149707743	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs587614510	chr1:149707746-149707747	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs587696047	chr1:149707755-149707756	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs373057849	chr1:149707780-149707781	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs200460325	chr1:149707917-149707918	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs587755628	chr1:149707947-149707948	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs7521655	chr1:149707973-149707974	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs61806470	chr1:149707988-149707989	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs1856687	chr1:149708021-149708022	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs587652955	chr1:149708043-149708044	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs587681761	chr1:149708047-149708048	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs375028683	chr1:149708072-149708073	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs587756633	chr1:149708090-149708091	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs587638014	chr1:149708166-149708167	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs111808641	chr1:149708177-149708178	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs61806471	chr1:149708210-149708211	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs199626725	chr1:149708213-149708214	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs369388259	chr1:149708214-149708215	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs200506659	chr1:149708216-149708217	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs587603294	chr1:149708241-149708242	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs587711897	chr1:149708315-149708316	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs201616973	chr1:149708430-149708431	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs587610867	chr1:149708527-149708528	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs199679933	chr1:149708654-149708655	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs587666083	chr1:149708678-149708679	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs111557391	chr1:149708691-149708692	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs200821477	chr1:149708704-149708705	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs201681330	chr1:149708740-149708741	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs587696728	chr1:149708772-149708773	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs587733069	chr1:149708798-149708799	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs587605363	chr1:149708858-149708859	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs587666756	chr1:149708903-149708904	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs12141520	chr1:149708908-149708909	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs12143862	chr1:149708909-149708910	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs587697932	chr1:149708956-149708957	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs587732792	chr1:149708975-149708976	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs587624624	chr1:149709017-149709018	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs6703046	chr1:149709040-149709041	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs75605391	chr1:149709093-149709094	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs587683542	chr1:149709101-149709102	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs587761416	chr1:149709102-149709103	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs76299414	chr1:149709116-149709117	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs7555401	chr1:149709188-149709189	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs587631069	chr1:149709196-149709197	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs373994778	chr1:149709204-149709205	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs587764991	chr1:149709245-149709246	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs61806474	chr1:149709259-149709260	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs587666346	chr1:149709260-149709261	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:115)

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
Cancer	21129771	CNVD
Non-small cell lung cancer	21385341	CNVD
Autosomal dominant nocturnal frontal lobe epilepsy	18472482	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thrombocytopenia-absent radius syndrome	21933853	CNVD
Psychiatric disorder	22848183	CNVD
Ewing''s sarcoma	21437220	CNVD
Liposarcoma	21253554	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Breast cancer	20409316	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	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
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Esophageal squamous carcinoma	18350619	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
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
Breast cancer	21611746	CNVD
Retinoblastoma	19183342	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Ewing''s sarcoma	17952124	CNVD
Osteosarcoma	19286668	CNVD
Osteosarcoma	17242211	CNVD
Ovarian cancer	17242211	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Schizophrenia	18990708	CNVD
Sudden cardiac death	19188705	CNVD
Plasma-cell dyscrasia	16705089	CNVD
Myeloma	17024118	CNVD
Cancer	17060936	CNVD
Multiple myeloma	16616336	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
Follicular lymphoma	18703704	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
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	21364760	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Myelofibrosis	22110671	CNVD
Liver carcinoma	19366792	CNVD
Testicular germ cell tumor	18059402	CNVD
Trisomy 5 syndrome	21098271	CNVD
Cancer	23975201	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:852 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:149707000-149711600	Weak transcription	Primary monocytes fromperipheralblood	blood
2	chr1:149711400-149711600	Enhancers	Primary neutrophils fromperipheralblood	blood
3	chr1:149711600-149711800	Enhancers	Primary T cells fromperipheralblood	blood
4	chr1:149711600-149711800	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr1:149711600-149711800	Enhancers	Placenta	Placenta
6	chr1:149711600-149712000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr1:149711600-149712000	Active TSS	HUES64 Cell Line	embryonic stem cell
8	chr1:149711600-149712000	Active TSS	Primary T helper naive cells from peripheral blood	blood
9	chr1:149711600-149712000	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
10	chr1:149711600-149712200	Active TSS	HUES48 Cell Line	embryonic stem cell
11	chr1:149711600-149712200	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr1:149711600-149712200	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
13	chr1:149711600-149712200	Enhancers	Primary B cells from cord blood	blood
14	chr1:149711600-149712400	Active TSS	HUES6 Cell Line	embryonic stem cell
15	chr1:149711600-149712400	Active TSS	iPS-18 Cell Line	embryonic stem cell
16	chr1:149711600-149712400	Enhancers	Primary monocytes fromperipheralblood	blood
17	chr1:149711600-149712400	Active TSS	Monocytes-CD14+_RO01746	blood
18	chr1:149711600-149712400	Active TSS	NHEK	skin
19	chr1:149711600-149712600	Active TSS	ES-I3 Cell Line	embryonic stem cell
20	chr1:149711600-149712600	Active TSS	H1 Cell Line	embryonic stem cell
21	chr1:149711600-149712600	Active TSS	H9 Cell Line	embryonic stem cell
22	chr1:149711600-149712600	Active TSS	iPS-15b Cell Line	embryonic stem cell
23	chr1:149711600-149712600	Active TSS	A549	lung
24	chr1:149711800-149712000	Bivalent/Poised TSS	IMR90 fetal lung fibroblasts Cell Line	lung
25	chr1:149711800-149712000	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
26	chr1:149711800-149712000	Active TSS	Primary T helper 17 cells PMA-I stimulated	--
27	chr1:149711800-149712000	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
28	chr1:149711800-149712000	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
29	chr1:149711800-149712000	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
30	chr1:149711800-149712000	Flanking Bivalent TSS/Enh	Duodenum Smooth Muscle	Duodenum
31	chr1:149711800-149712000	Flanking Active TSS	Placenta	Placenta
32	chr1:149711800-149712000	Active TSS	Pancreas	Pancrea
33	chr1:149711800-149712000	Active TSS	GM12878-XiMat	blood
34	chr1:149711800-149712200	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
35	chr1:149711800-149712200	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr1:149711800-149712200	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
37	chr1:149711800-149712200	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
38	chr1:149711800-149712200	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
39	chr1:149711800-149712200	Flanking Active TSS	Primary T cells fromperipheralblood	blood
40	chr1:149711800-149712200	Active TSS	Primary T regulatory cells fromperipheralblood	blood
41	chr1:149711800-149712200	Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
42	chr1:149711800-149712200	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
43	chr1:149711800-149712200	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin01	Skin
44	chr1:149711800-149712200	Bivalent/Poised TSS	Foreskin Melanocyte Primary Cells skin03	Skin
45	chr1:149711800-149712200	Active TSS	Primary mononuclear cells fromperipheralblood	Blood
46	chr1:149711800-149712200	Active TSS	Adipose Nuclei	Adipose
47	chr1:149711800-149712200	Active TSS	Brain Inferior Temporal Lobe	brain
48	chr1:149711800-149712200	Active TSS	Colonic Mucosa	Colon
49	chr1:149711800-149712200	Active TSS	Duodenum Mucosa	Duodenum
50	chr1:149711800-149712200	Active TSS	Pancreatic Islets	Pancreatic Islet

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