Variant report

Variant	nsv534981
Chromosome Location	chr1:61788310-61859074
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:907)
CpG islands
(count:183)
Chromatin interactive
region (count:40)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:907 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:61788431-61788823	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:61845384-61845804	HepG2	liver:	n/a	n/a
3	ARID3A	chr1:61858467-61858908	K562	blood:	n/a	n/a
4	ARID3A	chr1:61803582-61804220	HepG2	liver:	n/a	n/a
5	ARID3A	chr1:61804430-61805025	HepG2	liver:	n/a	chr1:61804472-61804488
6	ATF1	chr1:61822736-61822973	K562	blood:	n/a	n/a
7	ATF2	chr1:61803601-61804200	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF2	chr1:61797771-61798344	GM12878	blood:	n/a	n/a
9	ATF2	chr1:61798470-61798875	GM12878	blood:	n/a	n/a
10	ATF2	chr1:61798512-61798886	GM12878	blood:	n/a	n/a
11	ATF2	chr1:61797740-61798369	GM12878	blood:	n/a	n/a
12	ATF3	chr1:61803603-61803888	HepG2	liver:	n/a	n/a
13	ATF3	chr1:61803497-61804233	HCT-116	colon:	n/a	n/a
14	ATF3	chr1:61803497-61804277	A549	lung:	n/a	n/a
15	BATF	chr1:61853522-61853863	GM12878	blood:	n/a	n/a
16	BATF	chr1:61853544-61853838	GM12878	blood:	n/a	n/a
17	BATF	chr1:61797829-61798343	GM12878	blood:	n/a	chr1:61798030-61798039
18	BATF	chr1:61797824-61798390	GM12878	blood:	n/a	chr1:61798030-61798039
19	BATF	chr1:61798519-61798838	GM12878	blood:	n/a	n/a
20	BATF	chr1:61798509-61798813	GM12878	blood:	n/a	n/a
21	BCL11A	chr1:61797825-61798330	GM12878	blood:	n/a	n/a
22	BCL11A	chr1:61797889-61798186	GM12878	blood:	n/a	n/a
23	BCL11A	chr1:61798546-61798827	GM12878	blood:	n/a	n/a
24	BCL3	chr1:61797894-61798230	GM12878	blood:	n/a	n/a
25	BCLAF1	chr1:61797825-61798251	GM12878	blood:	n/a	n/a
26	BCLAF1	chr1:61797746-61798321	GM12878	blood:	n/a	n/a
27	BHLHE40	chr1:61797824-61798235	GM12878	blood:	n/a	n/a
28	BHLHE40	chr1:61858301-61858815	K562	blood:	n/a	n/a
29	BHLHE40	chr1:61803612-61804239	HepG2	liver:	n/a	n/a
30	BHLHE40	chr1:61847148-61847155	GM12878	blood:	n/a	n/a
31	CBX3	chr1:61803593-61804318	HCT-116	colon:	n/a	n/a
32	CBX3	chr1:61787806-61788345	K562	blood:	n/a	n/a
33	CBX3	chr1:61858370-61859040	K562	blood:	n/a	n/a
34	CBX3	chr1:61854815-61855267	K562	blood:	n/a	n/a
35	CBX3	chr1:61854920-61855190	K562	blood:	n/a	n/a
36	CEBPB	chr1:61788518-61788843	HepG2	liver:	n/a	n/a
37	CEBPB	chr1:61802714-61803054	H1-hESC	embryonic stem cell:	n/a	n/a
38	CEBPB	chr1:61802703-61802978	MCF-7	breast:	n/a	n/a
39	CEBPB	chr1:61788428-61788918	A549	lung:	n/a	n/a
40	CEBPB	chr1:61788459-61788892	A549	lung:	n/a	n/a
41	CEBPB	chr1:61800991-61801087	H1-hESC	embryonic stem cell:	n/a	n/a
42	CEBPB	chr1:61844554-61844609	K562	blood:	n/a	n/a
43	CEBPB	chr1:61790621-61790808	K562	blood:	n/a	chr1:61790739-61790748
44	CEBPB	chr1:61802739-61803016	HepG2	liver:	n/a	n/a
45	CEBPB	chr1:61797791-61798331	GM12878	blood:	n/a	chr1:61797985-61797996
46	CEBPB	chr1:61811719-61812018	HepG2	liver:	n/a	chr1:61811875-61811886
47	CEBPB	chr1:61820890-61821076	HepG2	liver:	n/a	chr1:61821010-61821023 chr1:61821011-61821022
48	CEBPB	chr1:61788444-61788945	MCF-7	breast:	n/a	n/a
49	CEBPB	chr1:61838597-61838951	HepG2	liver:	n/a	chr1:61838770-61838779 chr1:61838768-61838779
50	CEBPB	chr1:61804599-61804867	HepG2	liver:	n/a	chr1:61804732-61804741 chr1:61804732-61804743 chr1:61804730-61804743

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:61843430-61843480	GM12892	blood:	n/a
2	chr1:61848996-61849046	AoSMC	blood vessel:	n/a
3	chr1:61848996-61849046	IMR90	lung:	fetal
4	chr1:61803736-61803786	CMK	blood:	n/a
5	chr1:61803736-61803786	GM12891	blood:	n/a
6	chr1:61843430-61843480	MCF10A-Er-Src	breast:	n/a
7	chr1:61848996-61849046	LNCaP	prostate:	n/a
8	chr1:61843430-61843480	Hepatocyte	liver:	n/a
9	chr1:61803736-61803786	A549	lung:	n/a
10	chr1:61848996-61849046	NHBE	bronchial:	n/a
11	chr1:61803736-61803786	PrEC	prostate:	n/a
12	chr1:61803736-61803786	AG09309	skin:	n/a
13	chr1:61848996-61849046	HPAEpiC	pulmonary alveolar:	n/a
14	chr1:61843430-61843480	NB4	blood:	n/a
15	chr1:61843430-61843480	HMEC	breast:	n/a
16	chr1:61843430-61843480	Jurkat	blood:	n/a
17	chr1:61848996-61849046	HMEC	breast:	n/a
18	chr1:61843430-61843480	K562	blood:	n/a
19	chr1:61843430-61843480	GM12878	blood:	n/a
20	chr1:61848996-61849046	Jurkat	blood:	n/a
21	chr1:61843430-61843480	HCT-116	colon:	n/a
22	chr1:61848996-61849046	HEK293	kidney:	embryo
23	chr1:61803736-61803786	HPAEpiC	pulmonary alveolar:	n/a
24	chr1:61803736-61803786	HCT-116	colon:	n/a
25	chr1:61848996-61849046	Hepatocyte	liver:	n/a
26	chr1:61848996-61849046	AG10803	skin:	n/a
27	chr1:61803736-61803786	NHDF-neo	bronchial:	n/a
28	chr1:61843430-61843480	AoSMC	blood vessel:	n/a
29	chr1:61803736-61803786	U87	brain:	n/a
30	chr1:61848996-61849046	AG04450	lung:	fetal
31	chr1:61843430-61843480	SK-N-MC	brain:	n/a
32	chr1:61843430-61843480	HIPEpiC	eye:	n/a
33	chr1:61848996-61849046	HCPEpiC	choroid plexus:	n/a
34	chr1:61843430-61843480	Caco-2	colon:	n/a
35	chr1:61803736-61803786	GM12878	blood:	n/a
36	chr1:61848996-61849046	HEEpiC	esophagus:	n/a
37	chr1:61803736-61803786	AG04449	skin:	fetal
38	chr1:61843430-61843480	AG04449	skin:	fetal
39	chr1:61803736-61803786	RPTEC	kidney:	n/a
40	chr1:61843430-61843480	HAEpiC	amniotic membrane:	n/a
41	chr1:61803736-61803786	AoSMC	blood vessel:	n/a
42	chr1:61803736-61803786	ovcar-3	ovarian:	n/a
43	chr1:61848996-61849046	SK-N-SH_RA	brain:	n/a
44	chr1:61843430-61843480	HRE	kidney:	n/a
45	chr1:61843430-61843480	HEK293	kidney:	embryo
46	chr1:61843430-61843480	U87	brain:	n/a
47	chr1:61848996-61849046	SKMC	muscle:	n/a
48	chr1:61803736-61803786	MCF-7	breast:	n/a
49	chr1:61848996-61849046	MCF-7	breast:	n/a
50	chr1:61803736-61803786	SK-N-SH	brain:	n/a

(count:40 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:61805404..61807718-chr1:61819195..61821796,2	K562	blood:
2	chr1:61839086..61841387-chr1:61851332..61853518,2	K562	blood:
3	chr1:61821605..61823467-chr1:61848525..61850991,2	K562	blood:
4	chr1:61845747..61850628-chr1:61851992..61855233,6	K562	blood:
5	chr1:61803556..61804528-chr1:61918731..61919655,3	MCF-7	breast:
6	chr1:61838198..61840037-chr1:61852848..61854962,2	MCF-7	breast:
7	chr1:61821605..61823467-chr1:61848525..61850991,2	K562	blood:
8	chr1:61805404..61807718-chr1:61819195..61821796,2	K562	blood:
9	chr1:61856382..61859680-chr1:61860361..61865185,4	K562	blood:
10	chr1:61842507..61844898-chr1:61846678..61850358,3	K562	blood:
11	chr1:61842507..61844898-chr1:61846678..61850358,3	K562	blood:
12	chr1:61788026..61790559-chr1:61794700..61796416,2	MCF-7	breast:
13	chr1:61444776..61445376-chr1:61804008..61805059,3	MCF-7	breast:
14	chr1:61845747..61848557-chr1:61853337..61855233,2	K562	blood:
15	chr1:61784481..61786407-chr1:61788060..61789976,3	K562	blood:
16	chr1:61839086..61841387-chr1:61851332..61853518,2	K562	blood:
17	chr1:61605495..61608078-chr1:61787528..61789872,2	MCF-7	breast:
18	chr1:61772659..61774217-chr1:61790791..61792437,2	K562	blood:
19	chr1:61845747..61850628-chr1:61851992..61855233,6	K562	blood:
20	chr1:61821605..61824601-chr1:61847526..61850025,2	K562	blood:
21	chr1:61815681..61817818-chr1:61903758..61906179,2	K562	blood:
22	chr1:61838198..61840037-chr1:61852848..61854962,2	MCF-7	breast:
23	chr1:61444516..61445093-chr1:61815402..61816344,2	MCF-7	breast:
24	chr1:61816681..61819448-chr1:61820713..61822267,2	MCF-7	breast:
25	chr1:61802472..61805415-chr1:61917120..61919669,2	MCF-7	breast:
26	chr1:61813482..61815588-chr1:61817632..61819622,2	K562	blood:
27	chr1:61813440..61817104-chr1:61817540..61820998,4	K562	blood:
28	chr1:61809209..61811913-chr1:61823172..61825226,2	K562	blood:
29	chr1:61788026..61790559-chr1:61794700..61796416,2	MCF-7	breast:
30	chr1:61809209..61811913-chr1:61823172..61825226,2	K562	blood:
31	chr1:61821605..61824601-chr1:61847526..61850025,2	K562	blood:
32	chr1:61783085..61786028-chr1:61788145..61790007,2	MCF-7	breast:
33	chr1:61701605..61703264-chr1:61789061..61791484,2	K562	blood:
34	chr1:61748114..61750879-chr1:61800546..61802249,2	K562	blood:
35	chr1:61679578..61681382-chr1:61802246..61804281,2	MCF-7	breast:
36	chr1:61809086..61811561-chr1:61812317..61815281,2	K562	blood:
37	chr1:61515264..61516149-chr1:61803341..61804328,3	MCF-7	breast:
38	chr1:61856878..61859434-chr1:61872065..61873937,2	K562	blood:
39	chr1:61809086..61811561-chr1:61812317..61815281,2	K562	blood:
40	chr1:61845747..61848557-chr1:61853337..61855233,2	K562	blood:

No data

Variant related genes	Relation type
NFIA	TF binding region
NFIA	CpG island
ENSG00000162599	chromatin interactions

Extended variants
information (count: 2781 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:2781 , 50 per page) page: 1 2 3 4 5 6 7 ... 56

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs578120268	chr1:61788317-61788318	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs539147806	chr1:61788330-61788331	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs557890818	chr1:61788334-61788335	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs572991838	chr1:61788343-61788344	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs540502231	chr1:61788517-61788518	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs150235961	chr1:61788523-61788524	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs7518456	chr1:61788584-61788585	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs573618112	chr1:61788619-61788620	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs192820881	chr1:61788650-61788651	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs562153870	chr1:61788665-61788666	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs532816166	chr1:61788678-61788679	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs185291883	chr1:61788685-61788686	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs11810930	chr1:61788697-61788698	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs527915391	chr1:61788701-61788702	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs549631891	chr1:61788731-61788732	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs190168649	chr1:61788748-61788749	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs2806442	chr1:61788766-61788767	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs372114001	chr1:61788772-61788773	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs550160863	chr1:61788777-61788778	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs139268100	chr1:61788821-61788822	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs141602811	chr1:61788843-61788844	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs554005254	chr1:61788855-61788856	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs147065385	chr1:61788889-61788890	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs181155389	chr1:61788919-61788920	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs555552280	chr1:61788923-61788924	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs573557135	chr1:61788960-61788961	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs185598575	chr1:61788975-61788976	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs6675218	chr1:61788997-61788998	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs138434180	chr1:61789012-61789013	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs188055353	chr1:61789052-61789053	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs374355894	chr1:61789162-61789163	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs560018775	chr1:61789237-61789238	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs149561818	chr1:61789294-61789295	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs571692298	chr1:61789303-61789304	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs144249222	chr1:61789316-61789317	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs561477708	chr1:61789352-61789353	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs148269046	chr1:61789394-61789395	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs550545559	chr1:61789421-61789422	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs377058020	chr1:61789425-61789426	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs141367027	chr1:61789438-61789439	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs532576443	chr1:61789478-61789479	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs547789491	chr1:61789479-61789480	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs566003722	chr1:61789500-61789501	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs180916296	chr1:61789506-61789507	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs146229204	chr1:61789514-61789515	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs139313554	chr1:61789529-61789530	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs537739023	chr1:61789579-61789580	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs370119335	chr1:61789604-61789605	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs370039208	chr1:61789625-61789626	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs570773595	chr1:61789631-61789632	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:95)

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
Breast cancer	16620391	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
Ovarian cancer	21720365	CNVD
small cell lung cancer	20016488	CNVD
Developmental delay	21147756	CNVD
Breast cancer	17133270	CNVD
Myelofibrosis	22110671	CNVD
CNS Malformation Syndrome	17530927	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Type 2 diabetes	21956041	CNVD
Uveal melanoma	20484589	CNVD
Colorectal cancer	20459617	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Autism	20531469	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:1546 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:61744600-61798600	Weak transcription	Fetal Muscle Trunk	muscle
2	chr1:61778400-61792800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
3	chr1:61782200-61788600	Weak transcription	Fetal Brain Female	brain
4	chr1:61784000-61790000	Enhancers	Liver	Liver
5	chr1:61784600-61789600	Weak transcription	Right Ventricle	heart
6	chr1:61784800-61789600	Weak transcription	Aorta	Aorta
7	chr1:61784800-61789600	Weak transcription	Psoas Muscle	Psoas
8	chr1:61784800-61791400	Enhancers	Fetal Lung	lung
9	chr1:61784800-61799400	Weak transcription	Left Ventricle	heart
10	chr1:61784800-61800400	Weak transcription	Ovary	ovary
11	chr1:61784800-61802800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
12	chr1:61784800-61803200	Weak transcription	Rectal Mucosa Donor 31	rectum
13	chr1:61784800-61803600	Weak transcription	Sigmoid Colon	Sigmoid Colon
14	chr1:61785000-61797200	Weak transcription	HUVEC	blood vessel
15	chr1:61785000-61802400	Weak transcription	Primary hematopoietic stem cells	blood
16	chr1:61785000-61802400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr1:61785600-61789800	Weak transcription	Rectal Smooth Muscle	rectum
18	chr1:61785600-61791200	Enhancers	Breast Myoepithelial Primary Cells	Breast
19	chr1:61786000-61789600	Weak transcription	Small Intestine	intestine
20	chr1:61786000-61813600	Weak transcription	Duodenum Mucosa	Duodenum
21	chr1:61786200-61799000	Weak transcription	Fetal Intestine Large	intestine
22	chr1:61786400-61789600	Weak transcription	Stomach Smooth Muscle	stomach
23	chr1:61786400-61789800	Weak transcription	Fetal Muscle Leg	muscle
24	chr1:61786400-61798600	Weak transcription	Cortex derived primary cultured neurospheres	brain
25	chr1:61786600-61789600	Weak transcription	Fetal Heart	heart
26	chr1:61786600-61789800	Weak transcription	Fetal Stomach	stomach
27	chr1:61786600-61792400	Weak transcription	Right Atrium	heart
28	chr1:61786600-61799800	Weak transcription	Skeletal Muscle Female	skeletal muscle
29	chr1:61786600-61800400	Weak transcription	Brain Anterior Caudate	brain
30	chr1:61786600-61800400	Weak transcription	Colon Smooth Muscle	Colon
31	chr1:61786600-61800400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
32	chr1:61787000-61789600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr1:61787000-61790800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
34	chr1:61787200-61790600	Enhancers	HMEC	breast
35	chr1:61787800-61788400	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
36	chr1:61787800-61788400	Flanking Active TSS	NHEK	skin
37	chr1:61787800-61789400	Enhancers	Pancreatic Islets	Pancreatic Islet
38	chr1:61787800-61790600	Enhancers	HepG2	liver
39	chr1:61788000-61788400	Enhancers	Placenta	Placenta
40	chr1:61788000-61788400	Enhancers	Gastric	stomach
41	chr1:61788000-61789800	Enhancers	Stomach Mucosa	stomach
42	chr1:61788000-61790000	Enhancers	Hela-S3	cervix
43	chr1:61788000-61790600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
44	chr1:61788200-61788400	Genic enhancers	Pancreas	Pancrea
45	chr1:61788200-61788800	Flanking Active TSS	A549	lung
46	chr1:61788200-61789600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
47	chr1:61788200-61790000	Enhancers	K562	blood
48	chr1:61788400-61789200	Enhancers	NHEK	skin
49	chr1:61788400-61789800	Weak transcription	Pancreas	Pancrea
50	chr1:61788400-61792200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin

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