Variant report

Variant	nsv870486
Chromosome Location	chr1:74654182-74804833
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:730)
CpG islands
(count:918)
Chromatin interactive
region (count:28)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:730 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:74663686-74664378	K562	blood:	n/a	chr1:74664007-74664022
2	ARID3A	chr1:74663477-74664483	HepG2	liver:	n/a	chr1:74664007-74664022
3	ATF2	chr1:74662907-74663375	GM12878	blood:	n/a	n/a
4	ATF2	chr1:74710842-74711284	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr1:74663457-74664203	GM12878	blood:	n/a	n/a
6	ATF2	chr1:74710792-74711328	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr1:74721367-74721402	K562	blood:	n/a	n/a
8	BACH1	chr1:74721725-74721860	K562	blood:	n/a	n/a
9	BCL11A	chr1:74710883-74711156	H1-hESC	embryonic stem cell:	n/a	n/a
10	BCL11A	chr1:74710899-74711179	H1-hESC	embryonic stem cell:	n/a	n/a
11	BCLAF1	chr1:74663532-74664137	GM12878	blood:	n/a	chr1:74663930-74663943
12	BHLHE40	chr1:74746472-74746612	K562	blood:	n/a	n/a
13	BHLHE40	chr1:74663682-74664506	GM12878	blood:	n/a	n/a
14	BHLHE40	chr1:74665269-74665611	K562	blood:	n/a	n/a
15	BHLHE40	chr1:74665274-74665305	GM12878	blood:	n/a	n/a
16	BHLHE40	chr1:74663528-74664410	K562	blood:	n/a	n/a
17	BRCA1	chr1:74663561-74664177	Hela-S3	cervix:	n/a	n/a
18	CBX3	chr1:74663478-74664282	K562	blood:	n/a	n/a
19	CCNT2	chr1:74663575-74664088	K562	blood:	n/a	n/a
20	CEBPB	chr1:74764987-74765324	HepG2	liver:	n/a	chr1:74765155-74765166 chr1:74765142-74765150
21	CEBPB	chr1:74764993-74765325	A549	lung:	n/a	chr1:74765155-74765166 chr1:74765142-74765150
22	CEBPB	chr1:74710897-74711276	ECC-1	luminal epithelium:	n/a	n/a
23	CEBPB	chr1:74663659-74664198	Hela-S3	cervix:	n/a	n/a
24	CEBPB	chr1:74714756-74714989	HepG2	liver:	n/a	n/a
25	CEBPB	chr1:74768320-74768669	H1-hESC	embryonic stem cell:	n/a	n/a
26	CEBPB	chr1:74780245-74780491	H1-hESC	embryonic stem cell:	n/a	n/a
27	CEBPB	chr1:74777395-74777659	HepG2	liver:	n/a	chr1:74777540-74777553 chr1:74777541-74777552
28	CEBPB	chr1:74666607-74666817	HepG2	liver:	n/a	chr1:74666714-74666723 chr1:74666712-74666723
29	CEBPB	chr1:74783362-74783693	HepG2	liver:	n/a	n/a
30	CEBPB	chr1:74728463-74728579	HepG2	liver:	n/a	n/a
31	CEBPB	chr1:74662337-74662650	K562	blood:	n/a	n/a
32	CEBPB	chr1:74780146-74780463	IMR90	lung:	n/a	n/a
33	CEBPB	chr1:74664885-74665549	K562	blood:	n/a	n/a
34	CEBPB	chr1:74783464-74783590	HepG2	liver:	n/a	n/a
35	CEBPB	chr1:74729369-74729404	H1-hESC	embryonic stem cell:	n/a	chr1:74729392-74729403
36	CEBPB	chr1:74771504-74771688	HepG2	liver:	n/a	chr1:74771612-74771623
37	CEBPZ	chr1:74790846-74791124	HepG2	liver:	n/a	n/a
38	CHD1	chr1:74663275-74664217	GM12878	blood:	n/a	n/a
39	CHD2	chr1:74663569-74664035	K562	blood:	n/a	n/a
40	CHD2	chr1:74663618-74664320	Hela-S3	cervix:	n/a	n/a
41	CHD2	chr1:74663539-74664019	H1-hESC	embryonic stem cell:	n/a	n/a
42	CHD2	chr1:74663425-74664193	HepG2	liver:	n/a	n/a
43	CHD2	chr1:74663505-74664326	GM12878	blood:	n/a	n/a
44	CREB1	chr1:74663621-74664261	H1-hESC	embryonic stem cell:	n/a	n/a
45	CREB1	chr1:74663658-74664211	H1-hESC	embryonic stem cell:	n/a	n/a
46	CREB1	chr1:74663463-74664255	HepG2	liver:	n/a	n/a
47	CREB1	chr1:74663648-74664117	A549	lung:	n/a	n/a
48	CTCF	chr1:74737320-74737470	Hela-S3	cervix:	n/a	n/a
49	CTCF	chr1:74790800-74790950	HepG2	liver:	n/a	n/a
50	CTCF	chr1:74737315-74737416	H1-hESC	embryonic stem cell:	n/a	n/a

(count:918 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:74663583-74663633	T-47D	breast:	n/a
2	chr1:74663827-74663877	AG04450	lung:	fetal
3	chr1:74664160-74664210	NT2-D1	testis:	n/a
4	chr1:74663583-74663633	T-47D	breast:	n/a
5	chr1:74663827-74663877	AG04450	lung:	fetal
6	chr1:74664160-74664210	NT2-D1	testis:	n/a
7	chr1:74664132-74664182	SAEC	small airway:	n/a
8	chr1:74663921-74663971	PFSK-1	brain:	n/a
9	chr1:74663583-74663633	HRE	kidney:	n/a
10	chr1:74663297-74663347	HCPEpiC	choroid plexus:	n/a
11	chr1:74663927-74663977	NHDF-neo	bronchial:	n/a
12	chr1:74663927-74663977	SAEC	small airway:	n/a
13	chr1:74663680-74663730	CMK	blood:	n/a
14	chr1:74663899-74663949	AG10803	skin:	n/a
15	chr1:74663583-74663633	AG04449	skin:	fetal
16	chr1:74719316-74719366	SK-N-SH	brain:	n/a
17	chr1:74663297-74663347	SKMC	muscle:	n/a
18	chr1:74664132-74664182	SK-N-MC	brain:	n/a
19	chr1:74663680-74663730	GM06990	blood:	n/a
20	chr1:74663899-74663949	PFSK-1	brain:	n/a
21	chr1:74664061-74664111	SAEC	small airway:	n/a
22	chr1:74665362-74665412	U87	brain:	n/a
23	chr1:74663899-74663949	HUVEC	blood vessel:	n/a
24	chr1:74663636-74663686	H1-hESC	embryonic stem cell:	embryo
25	chr1:74663297-74663347	HCM	heart:	n/a
26	chr1:74664061-74664111	K562	blood:	n/a
27	chr1:74663921-74663971	HRE	kidney:	n/a
28	chr1:74666471-74666521	HRCEpiC	kidney:	n/a
29	chr1:74665362-74665412	CMK	blood:	n/a
30	chr1:74664061-74664111	AoSMC	blood vessel:	n/a
31	chr1:74664061-74664111	Caco-2	colon:	n/a
32	chr1:74666471-74666521	HEK293	kidney:	embryo
33	chr1:74663636-74663686	U87	brain:	n/a
34	chr1:74666471-74666521	K562	blood:	n/a
35	chr1:74663583-74663633	Hela-S3	cervix:	n/a
36	chr1:74665362-74665412	AG04449	skin:	fetal
37	chr1:74663750-74663800	MCF-7	breast:	n/a
38	chr1:74663297-74663347	Jurkat	blood:	n/a
39	chr1:74664132-74664182	SK-N-SH	brain:	n/a
40	chr1:74663680-74663730	Jurkat	blood:	n/a
41	chr1:74719316-74719366	ProgFib	skin:	n/a
42	chr1:74663680-74663730	PANC-1	pancreas:	n/a
43	chr1:74664160-74664210	MCF-7	breast:	n/a
44	chr1:74665362-74665412	HUVEC	blood vessel:	n/a
45	chr1:74665362-74665412	AG10803	skin:	n/a
46	chr1:74663680-74663730	HCF	heart:	n/a
47	chr1:74719316-74719366	HRPEpiC	eye:	n/a
48	chr1:74664160-74664210	GM06990	blood:	n/a
49	chr1:74663899-74663949	CMK	blood:	n/a
50	chr1:74719316-74719366	HRCEpiC	kidney:	n/a

(count:28 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:74678336..74683250-chr1:74684950..74687498,5	K562	blood:
2	chr1:74664371..74665891-chr1:74684150..74685886,2	K562	blood:
3	chr1:74725032..74727117-chr1:74729630..74732086,2	K562	blood:
4	chr1:74670579..74674137-chr1:74674462..74677110,4	K562	blood:
5	chr1:74701198..74703916-chr1:74780316..74782785,2	K562	blood:
6	chr1:74725032..74727117-chr1:74729630..74732086,2	K562	blood:
7	chr1:74692052..74694076-chr1:74701127..74702957,2	K562	blood:
8	chr1:74662984..74666783-chr1:74668983..74674031,7	K562	blood:
9	chr1:74677846..74679905-chr1:74682353..74684869,2	K562	blood:
10	chr1:74789903..74792042-chr1:74796412..74799113,2	MCF-7	breast:
11	chr1:74678336..74683250-chr1:74684950..74687498,5	K562	blood:
12	chr1:74662297..74664282-chr1:74667218..74669836,2	K562	blood:
13	chr1:74670579..74674137-chr1:74674462..74677110,4	K562	blood:
14	chr1:74789903..74792042-chr1:74796412..74799113,2	MCF-7	breast:
15	chr1:74662396..74665247-chr1:74681410..74684026,2	K562	blood:
16	chr1:74622416..74625063-chr1:74764779..74767346,2	K562	blood:
17	chr1:74677846..74679905-chr1:74682353..74684869,2	K562	blood:
18	chr1:74646951..74649028-chr1:74654609..74657361,2	K562	blood:
19	chr1:74725032..74727513-chr1:74728453..74731130,2	K562	blood:
20	chr1:74656254..74659150-chr1:74661430..74664103,3	K562	blood:
21	chr1:74649322..74651054-chr1:74653302..74655077,2	K562	blood:
22	chr1:74664371..74665891-chr1:74684150..74685886,2	K562	blood:
23	chr1:74701198..74703916-chr1:74780316..74782785,2	K562	blood:
24	chr1:74663449..74664076-chr20:1306022..1306565,2	Hela-S3	cervix:
25	chr1:74692052..74694076-chr1:74701127..74702957,2	K562	blood:
26	chr1:74725032..74727513-chr1:74728453..74731130,2	K562	blood:
27	chr1:74662960..74663950-chr9:131940135..131940948,2	Hela-S3	cervix:
28	chr1:74663942..74664482-chr7:25219741..25220347,2	NB4	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LRRC53-2	chr1:74663680-74663831	NONHSAT003957

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	FPGT	hsa-miR-335-5p	chr1:74672969-74672991

Variant related genes	Relation type
LRRIQ3	TF binding region
TNNI3K	TF binding region
FPGT-TNNI3K	TF binding region
FPGT	TF binding region
LRRIQ3	CpG island
TNNI3K	CpG island
FPGT-TNNI3K	CpG island
FPGT	CpG island
ENSG00000153790	chromatin interactions
ENSG00000116783	chromatin interactions
ENSG00000188483	chromatin interactions
ENSG00000125775	chromatin interactions
ENSG00000162620	chromatin interactions
ENSG00000234684	chromatin interactions
ENSG00000254685	chromatin interactions
ENSG00000259030	chromatin interactions

Extended variants
information (count: 5576 )
Associated
traits (count: 106 )

Variant overlapped rSNPs/rCNVs (count:5576 , 50 per page) page: 1 2 3 4 5 6 7 ... 112

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10789390	chr1:74654182-74654183	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs540304489	chr1:74654249-74654250	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs11210429	chr1:74654254-74654255	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs541209400	chr1:74654275-74654276	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs544287720	chr1:74654285-74654286	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs72962163	chr1:74654427-74654428	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs138911328	chr1:74654509-74654510	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs188149628	chr1:74654523-74654524	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs76894627	chr1:74654542-74654543	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs560650317	chr1:74654545-74654546	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs527912534	chr1:74654557-74654558	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs113237208	chr1:74654647-74654648	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs34315434	chr1:74654651-74654652	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs546643130	chr1:74654665-74654666	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs34965700	chr1:74654671-74654672	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs34565125	chr1:74654674-74654675	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs571265788	chr1:74654738-74654739	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs532082807	chr1:74654829-74654830	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs550301798	chr1:74654830-74654831	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs74991385	chr1:74654856-74654857	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs536121990	chr1:74654888-74654889	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs117230075	chr1:74654903-74654904	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs373790056	chr1:74654932-74654933	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs566302772	chr1:74654968-74654969	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs180988061	chr1:74654988-74654989	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs144722288	chr1:74655015-74655016	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs186361567	chr1:74655048-74655049	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs566719086	chr1:74655055-74655056	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs556268534	chr1:74655077-74655078	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs566372802	chr1:74655114-74655115	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs542515895	chr1:74655145-74655146	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs138524314	chr1:74655172-74655173	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs75845283	chr1:74655188-74655189	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs546085318	chr1:74655216-74655217	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs564746908	chr1:74655237-74655238	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs192485356	chr1:74655294-74655295	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs550682271	chr1:74655312-74655313	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs562119014	chr1:74655355-74655356	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs1930588	chr1:74655356-74655357	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
40	rs183379183	chr1:74655422-74655423	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs186824346	chr1:74655423-74655424	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs533940207	chr1:74655425-74655426	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs552079104	chr1:74655432-74655433	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs141488792	chr1:74655445-74655446	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs369125315	chr1:74655508-74655509	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs537930876	chr1:74655524-74655525	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs556720011	chr1:74655529-74655530	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs548768871	chr1:74655537-74655538	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs538874399	chr1:74655547-74655548	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs535861346	chr1:74655556-74655557	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:106)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Colorectal cancer	16272173	CNVD
Wilms tumour	21544195	CNVD
Coronary Disease	20032323	CNVD
Prostate cancer	21965145	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Stargardt''s disease	17277736	CNVD
Neuroblastoma	17897457	CNVD
Uveal melanoma	21693616	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-syndromic sensorineural hearing loss	22290220	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	21264507	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	17387387	CNVD
Oligodendroglial tumors	17285580	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Neuroblastoma	17535989	CNVD
Pheochromocytoma	17535989	CNVD
Prostate cancer	16705090	CNVD
Astrocytoma	17934521	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Neuroblastoma	17533364	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21385341	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Chordoma	21602918	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Melanoma	18172304	CNVD
Multiple myeloma	16461302	CNVD
Melanoma	17363583	CNVD
Cancer	21129771	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
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	20409316	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Rett syndrome	21593744	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
Ovarian cancer	21720365	CNVD
Breast cancer	17133270	CNVD
Type 2 diabetes	21956041	CNVD
Uveal melanoma	20484589	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
abnormal development	18461090	CNVD
Ewing''s sarcoma	17952124	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Poland''s syndrome	22110015	CNVD
Glioblastoma multiforme	22286061	CNVD
Glioblastoma multiforme	21922591	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Cancer	22429812	CNVD
Effusion lymphoma	18079361	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
small cell lung cancer	20016488	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:791 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:74659800-74660400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
2	chr1:74660400-74663200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
3	chr1:74660600-74660800	Enhancers	Primary hematopoietic stem cells short term culture	blood
4	chr1:74660600-74660800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
5	chr1:74660600-74660800	Enhancers	Primary T killer memory cells from peripheral blood	blood
6	chr1:74660800-74663200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
7	chr1:74661000-74663200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
8	chr1:74661600-74662800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
9	chr1:74662200-74663000	Enhancers	Dnd41	blood
10	chr1:74662400-74662800	Active TSS	GM12878-XiMat	blood
11	chr1:74662400-74662800	Enhancers	K562	blood
12	chr1:74662600-74663000	Enhancers	Primary T regulatory cells fromperipheralblood	blood
13	chr1:74662800-74663200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
14	chr1:74662800-74663200	Flanking Active TSS	GM12878-XiMat	blood
15	chr1:74662800-74663400	Enhancers	Primary T killer memory cells from peripheral blood	blood
16	chr1:74662800-74665800	Active TSS	K562	blood
17	chr1:74663000-74663200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
18	chr1:74663000-74663200	Enhancers	Primary B cells from cord blood	blood
19	chr1:74663000-74663200	Enhancers	Primary B cells from peripheral blood	blood
20	chr1:74663000-74663200	Enhancers	Primary hematopoietic stem cells	blood
21	chr1:74663000-74663200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
22	chr1:74663000-74663200	Enhancers	Primary T helper cells fromperipheralblood	blood
23	chr1:74663000-74663200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
24	chr1:74663000-74663200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
25	chr1:74663000-74663200	Enhancers	Adipose Nuclei	Adipose
26	chr1:74663000-74663200	Enhancers	Brain Hippocampus Middle	brain
27	chr1:74663000-74663200	Enhancers	A549	lung
28	chr1:74663000-74663200	Enhancers	Hela-S3	cervix
29	chr1:74663000-74663200	Enhancers	HepG2	liver
30	chr1:74663000-74663200	Enhancers	Monocytes-CD14+_RO01746	blood
31	chr1:74663000-74663200	Enhancers	Osteobl	bone
32	chr1:74663000-74663400	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
33	chr1:74663000-74663600	Flanking Active TSS	Dnd41	blood
34	chr1:74663000-74663800	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
35	chr1:74663000-74664400	Active TSS	Primary T cells from cord blood	blood
36	chr1:74663000-74664800	Active TSS	HMEC	breast
37	chr1:74663200-74663400	Enhancers	Primary monocytes fromperipheralblood	blood
38	chr1:74663200-74663400	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
39	chr1:74663200-74663400	Enhancers	Primary T helper naive cells from peripheral blood	blood
40	chr1:74663200-74663400	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
41	chr1:74663200-74663400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
42	chr1:74663200-74663400	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
43	chr1:74663200-74663400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
44	chr1:74663200-74663400	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
45	chr1:74663200-74663400	Enhancers	Fetal Thymus	thymus
46	chr1:74663200-74663400	Enhancers	Stomach Mucosa	stomach
47	chr1:74663200-74663400	Flanking Active TSS	Thymus	Thymus
48	chr1:74663200-74663400	Flanking Active TSS	A549	lung
49	chr1:74663200-74663400	Flanking Active TSS	Osteobl	bone
50	chr1:74663200-74663600	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

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