Variant report

Variant	nsv871269
Chromosome Location	chr1:74484753-74709362
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:696)
CpG islands
(count:915)
Chromatin interactive
region (count:30)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:696 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

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	chr1:74663457-74664203	GM12878	blood:	n/a	n/a
4	ATF2	chr1:74662907-74663375	GM12878	blood:	n/a	n/a
5	BACH1	chr1:74579087-74579383	H1-hESC	embryonic stem cell:	n/a	n/a
6	BCLAF1	chr1:74663532-74664137	GM12878	blood:	n/a	chr1:74663930-74663943
7	BHLHE40	chr1:74570008-74570023	GM12878	blood:	n/a	n/a
8	BHLHE40	chr1:74663682-74664506	GM12878	blood:	n/a	n/a
9	BHLHE40	chr1:74663528-74664410	K562	blood:	n/a	n/a
10	BHLHE40	chr1:74665274-74665305	GM12878	blood:	n/a	n/a
11	BHLHE40	chr1:74665269-74665611	K562	blood:	n/a	n/a
12	BRCA1	chr1:74663561-74664177	Hela-S3	cervix:	n/a	n/a
13	CBX3	chr1:74663478-74664282	K562	blood:	n/a	n/a
14	CCNT2	chr1:74663575-74664088	K562	blood:	n/a	n/a
15	CEBPB	chr1:74607672-74608043	IMR90	lung:	n/a	chr1:74607858-74607869
16	CEBPB	chr1:74646171-74646567	HepG2	liver:	n/a	chr1:74646354-74646365
17	CEBPB	chr1:74607787-74607950	K562	blood:	n/a	chr1:74607858-74607869
18	CEBPB	chr1:74627195-74627555	IMR90	lung:	n/a	n/a
19	CEBPB	chr1:74573018-74573040	H1-hESC	embryonic stem cell:	n/a	n/a
20	CEBPB	chr1:74646220-74646528	A549	lung:	n/a	chr1:74646354-74646365
21	CEBPB	chr1:74612576-74612806	H1-hESC	embryonic stem cell:	n/a	n/a
22	CEBPB	chr1:74646172-74646569	IMR90	lung:	n/a	chr1:74646354-74646365
23	CEBPB	chr1:74584352-74584643	H1-hESC	embryonic stem cell:	n/a	chr1:74584485-74584496
24	CEBPB	chr1:74664885-74665549	K562	blood:	n/a	n/a
25	CEBPB	chr1:74584311-74584580	HepG2	liver:	n/a	chr1:74584485-74584496
26	CEBPB	chr1:74662337-74662650	K562	blood:	n/a	n/a
27	CEBPB	chr1:74624760-74625022	IMR90	lung:	n/a	n/a
28	CEBPB	chr1:74666607-74666817	HepG2	liver:	n/a	chr1:74666714-74666723 chr1:74666712-74666723
29	CEBPB	chr1:74517121-74517299	HepG2	liver:	n/a	chr1:74517238-74517249
30	CEBPB	chr1:74646215-74646535	Hela-S3	cervix:	n/a	chr1:74646354-74646365
31	CEBPB	chr1:74607706-74607960	A549	lung:	n/a	chr1:74607858-74607869
32	CEBPB	chr1:74612627-74612820	K562	blood:	n/a	n/a
33	CEBPB	chr1:74646254-74646475	HepG2	liver:	n/a	chr1:74646354-74646365
34	CEBPB	chr1:74612578-74612900	IMR90	lung:	n/a	n/a
35	CEBPB	chr1:74612578-74612853	A549	lung:	n/a	n/a
36	CEBPB	chr1:74663659-74664198	Hela-S3	cervix:	n/a	n/a
37	CEBPB	chr1:74607709-74607977	HepG2	liver:	n/a	chr1:74607858-74607869
38	CEBPB	chr1:74584371-74584659	IMR90	lung:	n/a	chr1:74584485-74584496
39	CEBPB	chr1:74607706-74608010	Hela-S3	cervix:	n/a	chr1:74607858-74607869
40	CEBPB	chr1:74607713-74607984	H1-hESC	embryonic stem cell:	n/a	chr1:74607858-74607869
41	CHD1	chr1:74663275-74664217	GM12878	blood:	n/a	n/a
42	CHD2	chr1:74663425-74664193	HepG2	liver:	n/a	n/a
43	CHD2	chr1:74663618-74664320	Hela-S3	cervix:	n/a	n/a
44	CHD2	chr1:74663505-74664326	GM12878	blood:	n/a	n/a
45	CHD2	chr1:74663569-74664035	K562	blood:	n/a	n/a
46	CHD2	chr1:74663539-74664019	H1-hESC	embryonic stem cell:	n/a	n/a
47	CREB1	chr1:74663648-74664117	A549	lung:	n/a	n/a
48	CREB1	chr1:74663658-74664211	H1-hESC	embryonic stem cell:	n/a	n/a
49	CREB1	chr1:74663621-74664261	H1-hESC	embryonic stem cell:	n/a	n/a
50	CREB1	chr1:74663463-74664255	HepG2	liver:	n/a	n/a

(count:915 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:74663899-74663949	ovcar-3	ovarian:	n/a
2	chr1:74663750-74663800	PANC-1	pancreas:	n/a
3	chr1:74666471-74666521	NT2-D1	testis:	n/a
4	chr1:74664061-74664111	NT2-D1	testis:	n/a
5	chr1:74666471-74666521	AG10803	skin:	n/a
6	chr1:74663636-74663686	HepG2	liver:	n/a
7	chr1:74663921-74663971	HepG2	liver:	n/a
8	chr1:74663927-74663977	GM12891	blood:	n/a
9	chr1:74663636-74663686	SKMC	muscle:	n/a
10	chr1:74663583-74663633	Hepatocyte	liver:	n/a
11	chr1:74666471-74666521	HCM	heart:	n/a
12	chr1:74663297-74663347	GM19239	blood:	n/a
13	chr1:74663921-74663971	HAEpiC	amniotic membrane:	n/a
14	chr1:74664061-74664111	ovcar-3	ovarian:	n/a
15	chr1:74664061-74664111	ECC-1	luminal epithelium:	n/a
16	chr1:74664061-74664111	PrEC	prostate:	n/a
17	chr1:74663297-74663347	IMR90	lung:	fetal
18	chr1:74663583-74663633	AoSMC	blood vessel:	n/a
19	chr1:74663899-74663949	AG04450	lung:	fetal
20	chr1:74663680-74663730	BE2_C	brain:	n/a
21	chr1:74663636-74663686	PrEC	prostate:	n/a
22	chr1:74664061-74664111	U87	brain:	n/a
23	chr1:74665362-74665412	HL-60	blood:	n/a
24	chr1:74664132-74664182	SK-N-SH	brain:	n/a
25	chr1:74663921-74663971	PANC-1	pancreas:	n/a
26	chr1:74663899-74663949	T-47D	breast:	n/a
27	chr1:74665362-74665412	SKMC	muscle:	n/a
28	chr1:74664132-74664182	HRE	kidney:	n/a
29	chr1:74666471-74666521	HRCEpiC	kidney:	n/a
30	chr1:74663750-74663800	HRE	kidney:	n/a
31	chr1:74663583-74663633	HRPEpiC	eye:	n/a
32	chr1:74664132-74664182	K562	blood:	n/a
33	chr1:74620779-74620829	HL-60	blood:	n/a
34	chr1:74664132-74664182	BJ	skin:	n/a
35	chr1:74664061-74664111	AG09309	skin:	n/a
36	chr1:74663827-74663877	HCT-116	colon:	n/a
37	chr1:74663680-74663730	HRCEpiC	kidney:	n/a
38	chr1:74663927-74663977	AG04449	skin:	fetal
39	chr1:74663583-74663633	HRCEpiC	kidney:	n/a
40	chr1:74664160-74664210	GM12892	blood:	n/a
41	chr1:74620779-74620829	A549	lung:	n/a
42	chr1:74663636-74663686	NHDF-neo	bronchial:	n/a
43	chr1:74663827-74663877	AG09309	skin:	n/a
44	chr1:74663297-74663347	MCF10A-Er-Src	breast:	n/a
45	chr1:74664061-74664111	BE2_C	brain:	n/a
46	chr1:74663583-74663633	HPAEpiC	pulmonary alveolar:	n/a
47	chr1:74663827-74663877	IMR90	lung:	fetal
48	chr1:74664132-74664182	HPAEpiC	pulmonary alveolar:	n/a
49	chr1:74663827-74663877	NHBE	bronchial:	n/a
50	chr1:74664061-74664111	HEK293	kidney:	embryo

(count:30 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:74664371..74665891-chr1:74684150..74685886,2	K562	blood:
2	chr1:74662960..74663950-chr9:131940135..131940948,2	Hela-S3	cervix:
3	chr1:74677846..74679905-chr1:74682353..74684869,2	K562	blood:
4	chr1:74649322..74651054-chr1:74653302..74655077,2	K562	blood:
5	chr1:74610872..74613542-chr1:74663622..74665411,2	K562	blood:
6	chr1:74670579..74674137-chr1:74674462..74677110,4	K562	blood:
7	chr1:74678336..74683250-chr1:74684950..74687498,5	K562	blood:
8	chr1:74531200..74533536-chr1:74537407..74539060,2	K562	blood:
9	chr1:74663449..74664076-chr20:1306022..1306565,2	Hela-S3	cervix:
10	chr1:74641537..74643099-chr1:74809509..74811733,2	K562	blood:
11	chr1:74692052..74694076-chr1:74701127..74702957,2	K562	blood:
12	chr1:74532016..74533642-chr1:74533739..74535417,2	MCF-7	breast:
13	chr1:74622416..74625063-chr1:74764779..74767346,2	K562	blood:
14	chr1:74646951..74649028-chr1:74654609..74657361,2	K562	blood:
15	chr1:74613777..74616581-chr1:74619059..74620965,2	K562	blood:
16	chr1:74662297..74664282-chr1:74667218..74669836,2	K562	blood:
17	chr1:74692052..74694076-chr1:74701127..74702957,2	K562	blood:
18	chr1:74670579..74674137-chr1:74674462..74677110,4	K562	blood:
19	chr1:74664371..74665891-chr1:74684150..74685886,2	K562	blood:
20	chr1:74613777..74616581-chr1:74619059..74620965,2	K562	blood:
21	chr1:74203558..74206334-chr1:74548002..74550871,2	K562	blood:
22	chr1:74677846..74679905-chr1:74682353..74684869,2	K562	blood:
23	chr1:74531200..74533536-chr1:74537407..74539060,2	K562	blood:
24	chr1:74656254..74659150-chr1:74661430..74664103,3	K562	blood:
25	chr1:74663942..74664482-chr7:25219741..25220347,2	NB4	blood:
26	chr1:74662396..74665247-chr1:74681410..74684026,2	K562	blood:
27	chr1:74532016..74533642-chr1:74533739..74535417,2	MCF-7	breast:
28	chr1:74662984..74666783-chr1:74668983..74674031,7	K562	blood:
29	chr1:74678336..74683250-chr1:74684950..74687498,5	K562	blood:
30	chr1:74701198..74703916-chr1:74780316..74782785,2	K562	blood:

(count:8 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LRRC53-2	chr1:74663680-74663831	NONHSAT003957
2	lnc-LRRC53-2	chr1:74575078-74575237	NONHSAT003955
3	lnc-LRRC53-2	chr1:74549477-74549900	NONHSAT003955
4	lnc-LRRC53-2	chr1:74621417-74621533	NONHSAT003955
5	lnc-LRRC53-2	chr1:74560714-74560807	NONHSAT003955
6	lnc-LRRC53-2	chr1:74645907-74649368	NONHSAT003957
7	lnc-LRRC53-2	chr1:74621347-74621550	NONHSAT003956
8	lnc-LRRC53-2	chr1:74648222-74648306	NONHSAT003956

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
ENSG00000254685	chromatin interactions
ENSG00000125775	chromatin interactions
ENSG00000259030	chromatin interactions
ENSG00000188483	chromatin interactions
ENSG00000116783	chromatin interactions
ENSG00000153790	chromatin interactions
ENSG00000234684	chromatin interactions
ENSG00000162620	chromatin interactions

Extended variants
information (count: 2739 )
Associated
traits (count: 107 )

Variant overlapped rSNPs/rCNVs (count:2739 , 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	rs77428096	chr1:74538807-74538808	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs565908201	chr1:74538892-74538893	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs78837849	chr1:74538915-74538916	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs184661789	chr1:74538971-74538972	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs115481214	chr1:74538976-74538977	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs113063785	chr1:74538978-74538979	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs562060682	chr1:74539082-74539083	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs115810319	chr1:74539109-74539110	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs368219639	chr1:74539110-74539111	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs12742029	chr1:74539128-74539129	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs541195884	chr1:74539162-74539163	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs188586379	chr1:74539175-74539176	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs150618239	chr1:74539193-74539194	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs375364121	chr1:74539194-74539195	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs76692879	chr1:74541407-74541408	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs538641995	chr1:74541431-74541432	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs77907725	chr1:74541459-74541460	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs573943940	chr1:74541499-74541500	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs79383044	chr1:74541516-74541517	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs111440553	chr1:74541532-74541533	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs555162602	chr1:74541534-74541535	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs200559010	chr1:74541543-74541544	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs146775692	chr1:74541580-74541581	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs534528430	chr1:74541619-74541620	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs139548179	chr1:74541632-74541633	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs562755250	chr1:74541683-74541684	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs533173155	chr1:74541727-74541728	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs548999982	chr1:74542896-74542897	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs554365326	chr1:74542901-74542902	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs111233785	chr1:74543808-74543809	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs186072368	chr1:74543812-74543813	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs375595741	chr1:74543814-74543815	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs562633908	chr1:74543825-74543826	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs574638646	chr1:74543832-74543833	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs573954286	chr1:74543868-74543869	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs560483609	chr1:74543881-74543882	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs527803352	chr1:74543902-74543903	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs17589679	chr1:74543916-74543917	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs564697198	chr1:74543922-74543923	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs371034591	chr1:74543950-74543951	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs549649348	chr1:74546273-74546274	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs568155174	chr1:74546323-74546324	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs566745223	chr1:74546348-74546349	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs528947222	chr1:74546359-74546360	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs192487333	chr1:74546396-74546397	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs565844639	chr1:74546402-74546403	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs536685900	chr1:74546404-74546405	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs539778218	chr1:74546418-74546419	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs558009712	chr1:74546442-74546443	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs7355022	chr1:74546443-74546444	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:107)

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	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD

Chromatin state (count:628 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:74538800-74539200	Enhancers	Pancreas	Pancrea
2	chr1:74541400-74541800	Enhancers	Fetal Heart	heart
3	chr1:74546200-74546600	Enhancers	ES-I3 Cell Line	embryonic stem cell
4	chr1:74546200-74546600	Enhancers	HUES6 Cell Line	embryonic stem cell
5	chr1:74546200-74547200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr1:74571600-74572200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr1:74581000-74582200	Enhancers	ES-I3 Cell Line	embryonic stem cell
8	chr1:74581800-74582600	Enhancers	HUES48 Cell Line	embryonic stem cell
9	chr1:74603800-74604600	Active TSS	Adipose Nuclei	Adipose
10	chr1:74610600-74611000	Enhancers	Brain Substantia Nigra	brain
11	chr1:74610800-74611200	Enhancers	ES-I3 Cell Line	embryonic stem cell
12	chr1:74610800-74611200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr1:74610800-74611200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr1:74610800-74611200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
15	chr1:74610800-74611200	Enhancers	iPS-15b Cell Line	embryonic stem cell
16	chr1:74610800-74611200	Enhancers	Brain Anterior Caudate	brain
17	chr1:74610800-74611400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
18	chr1:74617000-74617600	Enhancers	iPS-18 Cell Line	embryonic stem cell
19	chr1:74617200-74617600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
20	chr1:74617200-74617600	Enhancers	iPS-20b Cell Line	embryonic stem cell
21	chr1:74622800-74623200	Enhancers	Adipose Nuclei	Adipose
22	chr1:74624200-74624800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr1:74624200-74624800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
24	chr1:74624800-74626000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
25	chr1:74624800-74626800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
26	chr1:74625600-74626000	Enhancers	Fetal Heart	heart
27	chr1:74625800-74626600	Enhancers	HMEC	breast
28	chr1:74626800-74627800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
29	chr1:74639800-74640200	Enhancers	HepG2	liver
30	chr1:74646000-74646800	Enhancers	Liver	Liver
31	chr1:74646000-74647000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr1:74646000-74647000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
33	chr1:74659800-74660400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
34	chr1:74660400-74663200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
35	chr1:74660600-74660800	Enhancers	Primary hematopoietic stem cells short term culture	blood
36	chr1:74660600-74660800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
37	chr1:74660600-74660800	Enhancers	Primary T killer memory cells from peripheral blood	blood
38	chr1:74660800-74663200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
39	chr1:74661000-74663200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
40	chr1:74661600-74662800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
41	chr1:74662200-74663000	Enhancers	Dnd41	blood
42	chr1:74662400-74662800	Active TSS	GM12878-XiMat	blood
43	chr1:74662400-74662800	Enhancers	K562	blood
44	chr1:74662600-74663000	Enhancers	Primary T regulatory cells fromperipheralblood	blood
45	chr1:74662800-74663200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
46	chr1:74662800-74663200	Flanking Active TSS	GM12878-XiMat	blood
47	chr1:74662800-74663400	Enhancers	Primary T killer memory cells from peripheral blood	blood
48	chr1:74662800-74665800	Active TSS	K562	blood
49	chr1:74663000-74663200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
50	chr1:74663000-74663200	Enhancers	Primary B cells from cord blood	blood

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