Variant report

Variant	nsv508583
Chromosome Location	chr10:51385007-51595892
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3692)
CpG islands
(count:3481)
Chromatin interactive
region (count:97)
LncRNA
region (count:17)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:3692 , 50 per page) page: 1 2 3 4 5 6 7 ... 74

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr10:51572002-51573003	HepG2	liver:	n/a	n/a
2	ARID3A	chr10:51519621-51519799	HepG2	liver:	n/a	n/a
3	ARID3A	chr10:51574489-51575240	HepG2	liver:	n/a	n/a
4	ARID3A	chr10:51593017-51593683	HepG2	liver:	n/a	n/a
5	ARID3A	chr10:51575722-51576490	K562	blood:	n/a	n/a
6	ARID3A	chr10:51593479-51595181	K562	blood:	n/a	n/a
7	ARID3A	chr10:51566359-51567345	HepG2	liver:	n/a	n/a
8	ARID3A	chr10:51575611-51576382	HepG2	liver:	n/a	n/a
9	ARID3A	chr10:51542999-51543673	HepG2	liver:	n/a	n/a
10	ARID3A	chr10:51565810-51567578	K562	blood:	n/a	n/a
11	ARID3A	chr10:51571787-51572845	K562	blood:	n/a	n/a
12	ARID3A	chr10:51574557-51575506	K562	blood:	n/a	n/a
13	ARID3A	chr10:51498525-51498807	HepG2	liver:	n/a	n/a
14	ARID3A	chr10:51564686-51565426	HepG2	liver:	n/a	n/a
15	ARID3A	chr10:51510620-51510822	HepG2	liver:	n/a	n/a
16	ARID3A	chr10:51559201-51560295	HepG2	liver:	n/a	n/a
17	ARID3A	chr10:51576767-51578015	K562	blood:	n/a	n/a
18	ARID3A	chr10:51563382-51564063	K562	blood:	n/a	n/a
19	ARID3A	chr10:51563320-51564285	HepG2	liver:	n/a	n/a
20	ARID3A	chr10:51589030-51589602	K562	blood:	n/a	n/a
21	ARID3A	chr10:51533675-51533676	K562	blood:	n/a	n/a
22	ATF1	chr10:51594027-51594614	K562	blood:	n/a	n/a
23	ATF1	chr10:51517350-51518597	K562	blood:	n/a	n/a
24	ATF1	chr10:51493021-51493256	K562	blood:	n/a	n/a
25	ATF1	chr10:51546430-51546741	K562	blood:	n/a	n/a
26	ATF1	chr10:51589227-51589534	K562	blood:	n/a	n/a
27	ATF1	chr10:51576865-51577414	K562	blood:	n/a	n/a
28	ATF1	chr10:51532222-51532656	K562	blood:	n/a	n/a
29	ATF2	chr10:51564921-51565404	GM12878	blood:	n/a	n/a
30	ATF2	chr10:51572161-51572907	GM12878	blood:	n/a	n/a
31	ATF2	chr10:51564903-51565407	GM12878	blood:	n/a	n/a
32	ATF2	chr10:51564835-51565406	H1-hESC	embryonic stem cell:	n/a	n/a
33	ATF3	chr10:51572332-51572767	K562	blood:	n/a	n/a
34	ATF3	chr10:51594081-51594640	K562	blood:	n/a	n/a
35	BACH1	chr10:51488154-51489051	K562	blood:	n/a	n/a
36	BACH1	chr10:51593692-51595261	K562	blood:	n/a	n/a
37	BACH1	chr10:51571391-51572968	K562	blood:	n/a	chr10:51572675-51572689
38	BACH1	chr10:51497179-51497372	H1-hESC	embryonic stem cell:	n/a	n/a
39	BACH1	chr10:51515004-51515258	K562	blood:	n/a	n/a
40	BACH1	chr10:51564903-51565765	H1-hESC	embryonic stem cell:	n/a	n/a
41	BACH1	chr10:51575186-51576144	K562	blood:	n/a	n/a
42	BACH1	chr10:51552569-51553373	H1-hESC	embryonic stem cell:	n/a	n/a
43	BACH1	chr10:51572033-51572783	H1-hESC	embryonic stem cell:	n/a	chr10:51572675-51572689
44	BACH1	chr10:51488208-51489253	H1-hESC	embryonic stem cell:	n/a	n/a
45	BATF	chr10:51572499-51572773	GM12878	blood:	n/a	n/a
46	BCL11A	chr10:51477990-51478142	GM12878	blood:	n/a	n/a
47	BCL11A	chr10:51502600-51502958	GM12878	blood:	n/a	n/a
48	BCL11A	chr10:51572342-51572790	GM12878	blood:	n/a	n/a
49	BCL3	chr10:51572404-51572755	GM12878	blood:	n/a	n/a
50	BCLAF1	chr10:51572069-51572688	K562	blood:	n/a	chr10:51572201-51572214

(count:3481 , 50 per page) page: 1 2 3 4 5 6 7 ... 70

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:51567670-51567720	HEEpiC	esophagus:	n/a
2	chr10:51572216-51572266	CMK	blood:	n/a
3	chr10:51571611-51571661	HEEpiC	esophagus:	n/a
4	chr10:51465444-51465494	HRPEpiC	eye:	n/a
5	chr10:51567670-51567720	HEEpiC	esophagus:	n/a
6	chr10:51572216-51572266	CMK	blood:	n/a
7	chr10:51571611-51571661	HEEpiC	esophagus:	n/a
8	chr10:51465444-51465494	HRPEpiC	eye:	n/a
9	chr10:51548083-51548133	ovcar-3	ovarian:	n/a
10	chr10:51576452-51576502	NHBE	bronchial:	n/a
11	chr10:51488973-51489023	HEEpiC	esophagus:	n/a
12	chr10:51566824-51566874	ProgFib	skin:	n/a
13	chr10:51550114-51550164	A549	lung:	n/a
14	chr10:51589507-51589557	AG09309	skin:	n/a
15	chr10:51572203-51572253	T-47D	breast:	n/a
16	chr10:51582891-51582941	H1-hESC	embryonic stem cell:	embryo
17	chr10:51575592-51575642	ProgFib	skin:	n/a
18	chr10:51565087-51565137	HCM	heart:	n/a
19	chr10:51572113-51572163	HL-60	blood:	n/a
20	chr10:51468217-51468267	HRE	kidney:	n/a
21	chr10:51549499-51549549	PFSK-1	brain:	n/a
22	chr10:51572203-51572253	U87	brain:	n/a
23	chr10:51572458-51572508	HAEpiC	amniotic membrane:	n/a
24	chr10:51549499-51549549	K562	blood:	n/a
25	chr10:51576241-51576291	MCF10A-Er-Src	breast:	n/a
26	chr10:51548895-51548945	HCF	heart:	n/a
27	chr10:51572570-51572620	NHDF-neo	bronchial:	n/a
28	chr10:51566202-51566252	MCF10A-Er-Src	breast:	n/a
29	chr10:51565087-51565137	NH-A	brain:	n/a
30	chr10:51572113-51572163	RPTEC	kidney:	n/a
31	chr10:51487558-51487608	PFSK-1	brain:	n/a
32	chr10:51548895-51548945	HNPCEpiC	eye:	n/a
33	chr10:51582891-51582941	GM12891	blood:	n/a
34	chr10:51589507-51589557	HUVEC	blood vessel:	n/a
35	chr10:51566202-51566252	HCPEpiC	choroid plexus:	n/a
36	chr10:51553061-51553111	HUVEC	blood vessel:	n/a
37	chr10:51487635-51487685	HCF	heart:	n/a
38	chr10:51567670-51567720	LNCaP	prostate:	n/a
39	chr10:51566824-51566874	SK-N-SH_RA	brain:	n/a
40	chr10:51489223-51489273	NB4	blood:	n/a
41	chr10:51468217-51468267	HepG2	liver:	n/a
42	chr10:51550114-51550164	Jurkat	blood:	n/a
43	chr10:51548083-51548133	NHDF-neo	bronchial:	n/a
44	chr10:51532379-51532429	SK-N-SH_RA	brain:	n/a
45	chr10:51550114-51550164	GM12878	blood:	n/a
46	chr10:51525504-51525554	HCM	heart:	n/a
47	chr10:51468217-51468267	NHBE	bronchial:	n/a
48	chr10:51564773-51564823	HRPEpiC	eye:	n/a
49	chr10:51489980-51490030	HCT-116	colon:	n/a
50	chr10:51572303-51572353	GM12892	blood:	n/a

(count:97 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr10:47653734..47654656-chr10:51488800..51489544,4	MCF-7	breast:
2	chr10:51581251..51582790-chr10:51586063..51588597,2	MCF-7	breast:
3	chr10:51583528..51586530-chr10:51586774..51590524,3	K562	blood:
4	chr10:51572414..51574084-chr10:51576253..51578988,2	MCF-7	breast:
5	chr10:51565658..51569040-chr10:51588313..51591211,4	MCF-7	breast:
6	chr10:51584103..51585748-chr10:51590752..51592260,2	K562	blood:
7	chr10:51532580..51534464-chr10:51540648..51542621,2	MCF-7	breast:
8	chr10:51547084..51547969-chr10:51561611..51562558,5	MCF-7	breast:
9	chr10:49495690..49496196-chr10:51547486..51547990,2	MCF-7	breast:
10	chr10:51529774..51532787-chr10:51533205..51535584,3	K562	blood:
11	chr10:51488667..51489638-chr19:9250701..9251449,2	NB4	blood:
12	chr10:51519873..51522291-chr10:51523430..51526195,2	MCF-7	breast:
13	chr10:51535106..51538475-chr10:51540322..51544715,4	MCF-7	breast:
14	chr10:51578985..51580681-chr10:51582739..51584284,2	MCF-7	breast:
15	chr10:51530063..51532648-chr10:51547234..51548849,2	MCF-7	breast:
16	chr10:51573053..51576531-chr10:51578356..51581811,4	MCF-7	breast:
17	chr10:51556994..51558686-chr6:27775677..27777979,2	MCF-7	breast:
18	chr10:51533109..51536566-chr10:51563798..51566935,3	K562	blood:
19	chr10:51583528..51586530-chr10:51586774..51590524,3	K562	blood:
20	chr10:51577976..51580402-chr10:51589650..51592528,2	K562	blood:
21	chr10:51566865..51573381-chr10:51591747..51595936,8	K562	blood:
22	chr10:47653740..47654385-chr10:51488816..51489933,3	MCF-7	breast:
23	chr10:51559473..51561873-chr10:51565294..51567542,2	MCF-7	breast:
24	chr10:51543087..51545887-chr10:51546426..51548810,3	K562	blood:
25	chr10:51588281..51590729-chr10:51592632..51595243,5	K562	blood:
26	chr10:51546403..51547918-chr10:51562484..51564984,2	K562	blood:
27	chr10:51546403..51547918-chr10:51562484..51564984,2	K562	blood:
28	chr10:51585950..51588362-chr10:51590669..51592514,2	MCF-7	breast:
29	chr10:51531433..51533993-chr10:51534075..51536056,4	MCF-7	breast:
30	chr10:51547408..51548033-chr10:51572070..51572901,3	MCF-7	breast:
31	chr10:51564159..51566794-chr10:51591562..51595707,4	K562	blood:
32	chr10:51529937..51532713-chr10:51550229..51551765,2	K562	blood:
33	chr10:47654306..47654893-chr10:51488919..51489481,3	MCF-7	breast:
34	chr10:51584103..51585748-chr10:51590752..51592260,2	K562	blood:
35	chr10:51535395..51539770-chr10:51541665..51546019,6	MCF-7	breast:
36	chr10:51570592..51573850-chr10:51592863..51596570,5	K562	blood:
37	chr10:51547408..51548033-chr10:51572291..51572901,2	MCF-7	breast:
38	chr10:51547084..51547969-chr10:51561611..51562558,5	MCF-7	breast:
39	chr10:51564909..51568960-chr10:51591606..51594482,5	K562	blood:
40	chr10:51535395..51539770-chr10:51541665..51546019,6	MCF-7	breast:
41	chr10:51574397..51577698-chr10:51592269..51595916,4	K562	blood:
42	chr10:47654140..47654870-chr10:51488638..51489755,11	HCT-116	colon:
43	chr10:51497870..51501630-chr10:51543327..51546015,3	MCF-7	breast:
44	chr10:51547397..51547921-chr10:51555333..51556233,2	MCF-7	breast:
45	chr10:51546570..51548123-chr10:51565132..51567244,2	K562	blood:
46	chr10:51577369..51580792-chr10:51592751..51595970,6	K562	blood:
47	chr10:51487738..51490469-chr10:51490768..51492273,2	MCF-7	breast:
48	chr10:51547501..51548076-chr10:51561750..51562345,2	MCF-7	breast:
49	chr10:51547084..51547807-chr10:51561632..51562558,5	MCF-7	breast:
50	chr10:51572414..51574084-chr10:51576253..51578988,2	MCF-7	breast:

(count:17 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NCOA4-1	chr10:51562271-51562493	NONHSAT013346
2	lnc-NCOA4-1	chr10:51553249-51553348	NONHSAT013344
3	lnc-NCOA4-1	chr10:51549553-51549587	NONHSAT013343
4	lnc-NCOA4-1	chr10:51555731-51555836	NONHSAT013344
5	lnc-NCOA4-1	chr10:51556751-51556856	NONHSAT013346
6	lnc-NCOA4-1	chr10:51555731-51555836	NONHSAT013343
7	lnc-NCOA4-1	chr10:51556751-51556856	NONHSAT013344
8	lnc-NCOA4-1	chr10:51549553-51549587	NONHSAT013344
9	lnc-NCOA4-1	chr10:51550041-51550174	NONHSAT013346
10	lnc-NCOA4-1	chr10:51549553-51549587	NONHSAT013346
11	lnc-NCOA4-1	chr10:51555731-51555836	NONHSAT013346
12	lnc-NCOA4-1	chr10:51550041-51550174	NONHSAT013344
13	lnc-NCOA4-1	chr10:51562271-51562451	NONHSAT013344
14	lnc-NCOA4-1	chr10:51557353-51560266	NONHSAT013347
15	lnc-NCOA4-1	chr10:51555731-51556409	NONHSAT013345
16	lnc-NCOA4-1	chr10:51549553-51549587	NONHSAT013345
17	lnc-NCOA4-1	chr10:51556751-51557360	NONHSAT013343

No data

Variant related genes	Relation type
ENSG00000228326	TF binding region
AGAP7	TF binding region
TIMM23	TF binding region
MSMB	TF binding region
NCOA4	TF binding region
ENSG00000230553	TF binding region
ENSG00000228326	CpG island
AGAP7	CpG island
TIMM23	CpG island
MSMB	CpG island
NCOA4	CpG island
ENSG00000230553	CpG island
ENSG00000203813	chromatin interactions
ENSG00000138293	chromatin interactions
ENSG00000138297	chromatin interactions
ENSG00000165406	chromatin interactions
ENSG00000259942	chromatin interactions
ENSG00000138294	chromatin interactions
ENSG00000130803	chromatin interactions
ENSG00000185130	chromatin interactions
ENSG00000198250	chromatin interactions
ENSG00000230553	chromatin interactions
ENSG00000196747	chromatin interactions
ENSG00000228326	chromatin interactions

Extended variants
information (count: 4795 )
Associated
traits (count: 74 )

Variant overlapped rSNPs/rCNVs (count:4795 , 50 per page) page: 1 2 3 4 5 6 7 ... 96

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs61849533	chr10:51385082-51385083	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs61849534	chr10:51385139-51385140	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs61849535	chr10:51385227-51385228	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs61849536	chr10:51385233-51385234	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs61849537	chr10:51385282-51385283	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs201450632	chr10:51385464-51385465	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs374157458	chr10:51385578-51385579	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs377293623	chr10:51385582-51385583	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs547932209	chr10:51385709-51385710	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs369724889	chr10:51385742-51385743	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs566156699	chr10:51385754-51385755	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs539853715	chr10:51385759-51385760	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs557856610	chr10:51385766-51385767	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs61849539	chr10:51386257-51386258	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs61849540	chr10:51386284-51386285	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs569987792	chr10:51386705-51386706	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs536957655	chr10:51386706-51386707	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs111423220	chr10:51386748-51386749	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs555208499	chr10:51387162-51387163	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs376993508	chr10:51387180-51387181	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs375576482	chr10:51387921-51387922	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs201842428	chr10:51388051-51388052	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs202198383	chr10:51388075-51388076	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs4962284	chr10:51388287-51388288	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs61849549	chr10:51388418-51388419	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs112374367	chr10:51388557-51388558	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs61849550	chr10:51388622-51388623	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs61849551	chr10:51388636-51388637	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs61849552	chr10:51388685-51388686	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs61849553	chr10:51388698-51388699	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs144676148	chr10:51389052-51389053	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs59211689	chr10:51389083-51389084	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs79543514	chr10:51389108-51389109	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs200246530	chr10:51389519-51389520	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs201733100	chr10:51389521-51389522	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs186527694	chr10:51390052-51390053	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs572693336	chr10:51390889-51390890	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs544517467	chr10:51461806-51461807	Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs79489567	chr10:51461808-51461809	Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs529950092	chr10:51461825-51461826	Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs75074999	chr10:51461838-51461839	Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs79368032	chr10:51461859-51461860	Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs377626318	chr10:51461870-51461871	Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs191638130	chr10:51461884-51461885	Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs183153884	chr10:51461885-51461886	Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs539730315	chr10:51461927-51461928	Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs187107924	chr10:51461950-51461951	Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs570446028	chr10:51461993-51461994	Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs549703743	chr10:51462016-51462017	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs537412607	chr10:51462048-51462049	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:74)

Disease	PMID	Source
Pancreatic endocrine tumor	17639061	CNVD
Gastric cancer	17908304	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Melanoma	18172304	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Ewing''s sarcoma	17952124	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	20724749	CNVD
Autism	22495311	CNVD
Esophageal cancer	21851588	CNVD
Prostate cancer	18632612	CNVD
Autism	18414403	CNVD
Cockayne syndrome	18421352	CNVD
Glioblastoma	16823260	CNVD
Medulloblastoma	16968546	CNVD
Neuroblastoma	17533364	CNVD
Cancer	21183584	CNVD
T-cell lymphomas	19863542	CNVD
Testicular germ cell tumor	18059402	CNVD
Squamous cell cancer	21044232	CNVD
Glioma	21971842	CNVD
Cancer	21637783	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Obesity	21956041	CNVD
Renal cell carcinoma	18765545	CNVD
Developmental delay	21948486	CNVD
Dysmorphic features	21948486	CNVD
Epilepsy	21948486	CNVD
Breast cancer	21785460	CNVD
Intellectual disability	21948486	CNVD
Intellectual disability	22045946	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Lung cancer	18438408	CNVD
Autism	22543975	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
skeletal anomalies	21948486	CNVD
Autism	21948486	CNVD
speech delay	21948486	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	21990379	CNVD
Myelofibrosis	22110671	CNVD
Metanephric adenoma	20802469	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Colorectal cancer	21645411	CNVD
Lung adenocarcinoma	21935476	CNVD
early-passage human iPS cells	21368824	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Melanoma	17363583	CNVD

Chromatin state (count:3430 , 50 per page) page: 1 2 3 4 5 6 7 ... 69

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:51372200-51391000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
2	chr10:51461800-51462000	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr10:51462000-51467000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr10:51464000-51466400	Weak transcription	Thymus	Thymus
5	chr10:51486600-51488200	Weak transcription	Right Atrium	heart
6	chr10:51486600-51488800	Weak transcription	Lung	lung
7	chr10:51487400-51487600	Enhancers	Primary B cells from peripheral blood	blood
8	chr10:51487400-51488200	Enhancers	Monocytes-CD14+_RO01746	blood
9	chr10:51487600-51487800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr10:51487600-51487800	Bivalent Enhancer	iPS DF 6.9 Cell Line	embryonic stem cell
11	chr10:51487600-51487800	Bivalent Enhancer	Primary hematopoietic stem cells	blood
12	chr10:51487600-51488000	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
13	chr10:51487600-51488000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr10:51487600-51488000	Enhancers	Gastric	stomach
15	chr10:51487600-51488000	Enhancers	K562	blood
16	chr10:51487600-51488200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
17	chr10:51487600-51488200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr10:51487600-51488200	Enhancers	Primary monocytes fromperipheralblood	blood
19	chr10:51487600-51488200	Enhancers	Primary neutrophils fromperipheralblood	blood
20	chr10:51487600-51488200	Enhancers	Primary hematopoietic stem cells short term culture	blood
21	chr10:51487600-51488200	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
22	chr10:51487600-51488200	Enhancers	Fetal Thymus	thymus
23	chr10:51487600-51488200	Enhancers	Pancreas	Pancrea
24	chr10:51487600-51488200	Enhancers	Skeletal Muscle Female	skeletal muscle
25	chr10:51487600-51488200	Enhancers	Thymus	Thymus
26	chr10:51487600-51488400	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
27	chr10:51487600-51488400	Bivalent Enhancer	HepG2	liver
28	chr10:51487600-51488800	Enhancers	Spleen	Spleen
29	chr10:51487800-51488400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
30	chr10:51488000-51488200	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr10:51488000-51488200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
32	chr10:51488000-51488200	Enhancers	Hela-S3	cervix
33	chr10:51488000-51488400	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
34	chr10:51488000-51488400	Weak transcription	Gastric	stomach
35	chr10:51488200-51488400	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
36	chr10:51488200-51488400	Bivalent/Poised TSS	H1 Cell Line	embryonic stem cell
37	chr10:51488200-51488400	Bivalent Enhancer	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
38	chr10:51488200-51488400	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
39	chr10:51488200-51488400	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
40	chr10:51488200-51488400	Bivalent Enhancer	Primary B cells from cord blood	blood
41	chr10:51488200-51488400	Enhancers	Primary T cells from cord blood	blood
42	chr10:51488200-51488400	Bivalent Enhancer	Primary hematopoietic stem cells short term culture	blood
43	chr10:51488200-51488400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
44	chr10:51488200-51488400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
45	chr10:51488200-51488400	Bivalent Enhancer	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
46	chr10:51488200-51488400	Bivalent Enhancer	Ganglion Eminence derived primary cultured neurospheres	brain
47	chr10:51488200-51488400	Enhancers	Brain Cingulate Gyrus	brain
48	chr10:51488200-51488400	Bivalent Enhancer	Brain Germinal Matrix	brain
49	chr10:51488200-51488400	Bivalent Enhancer	Colon Smooth Muscle	Colon
50	chr10:51488200-51488400	Bivalent Enhancer	Duodenum Mucosa	Duodenum

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