Variant report

Variant	nsv916868
Chromosome Location	chr1:61700430-62119762
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:4279)
CpG islands
(count:1344)
Chromatin interactive
region (count:230)
LncRNA
region (count:23)
Mature miRNA
region (count: 0)
miRNA target
sites (count:7)

(count:4279 , 50 per page) page: 1 2 3 4 5 6 7 ... 86

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:61918792-61919337	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:62054400-62054600	HepG2	liver:	n/a	n/a
3	ARID3A	chr1:61729696-61730064	HepG2	liver:	n/a	n/a
4	ARID3A	chr1:61916231-61916610	HepG2	liver:	n/a	n/a
5	ARID3A	chr1:61775741-61775966	K562	blood:	n/a	n/a
6	ARID3A	chr1:61734343-61734397	K562	blood:	n/a	n/a
7	ARID3A	chr1:61734451-61734609	HepG2	liver:	n/a	n/a
8	ARID3A	chr1:61765298-61765498	HepG2	liver:	n/a	n/a
9	ARID3A	chr1:61736169-61737649	K562	blood:	n/a	n/a
10	ARID3A	chr1:61783930-61784180	K562	blood:	n/a	n/a
11	ARID3A	chr1:61707760-61707818	K562	blood:	n/a	n/a
12	ARID3A	chr1:61747916-61748342	HepG2	liver:	n/a	n/a
13	ARID3A	chr1:61758895-61759118	HepG2	liver:	n/a	n/a
14	ARID3A	chr1:61703799-61704606	K562	blood:	n/a	n/a
15	ARID3A	chr1:61845384-61845804	HepG2	liver:	n/a	n/a
16	ARID3A	chr1:61918159-61918530	HepG2	liver:	n/a	chr1:61918420-61918436
17	ARID3A	chr1:61720404-61720608	K562	blood:	n/a	chr1:61720562-61720578
18	ARID3A	chr1:61730313-61730506	K562	blood:	n/a	n/a
19	ARID3A	chr1:61918730-61919187	K562	blood:	n/a	chr1:61918746-61918762 chr1:61918747-61918763
20	ARID3A	chr1:61912315-61912668	K562	blood:	n/a	n/a
21	ARID3A	chr1:61718825-61719543	K562	blood:	n/a	n/a
22	ARID3A	chr1:61803582-61804220	HepG2	liver:	n/a	n/a
23	ARID3A	chr1:61730347-61731058	HepG2	liver:	n/a	n/a
24	ARID3A	chr1:61804430-61805025	HepG2	liver:	n/a	chr1:61804472-61804488
25	ARID3A	chr1:62112891-62113154	HepG2	liver:	n/a	n/a
26	ARID3A	chr1:61788431-61788823	HepG2	liver:	n/a	n/a
27	ARID3A	chr1:61858467-61858908	K562	blood:	n/a	n/a
28	ARID3A	chr1:61785452-61785818	HepG2	liver:	n/a	n/a
29	ATF1	chr1:61775799-61776079	K562	blood:	n/a	n/a
30	ATF1	chr1:61907454-61907689	K562	blood:	n/a	n/a
31	ATF1	chr1:62106776-62107045	K562	blood:	n/a	n/a
32	ATF1	chr1:61736496-61737130	K562	blood:	n/a	n/a
33	ATF1	chr1:61918712-61919411	K562	blood:	n/a	n/a
34	ATF1	chr1:61719037-61719424	K562	blood:	n/a	n/a
35	ATF1	chr1:61822736-61822973	K562	blood:	n/a	n/a
36	ATF1	chr1:61970649-61970845	K562	blood:	n/a	n/a
37	ATF1	chr1:61912403-61912671	K562	blood:	n/a	n/a
38	ATF1	chr1:61727251-61727255	K562	blood:	n/a	n/a
39	ATF1	chr1:61783897-61784315	K562	blood:	n/a	n/a
40	ATF2	chr1:61784270-61784940	GM12878	blood:	n/a	n/a
41	ATF2	chr1:61918708-61919362	H1-hESC	embryonic stem cell:	n/a	n/a
42	ATF2	chr1:61918763-61919244	H1-hESC	embryonic stem cell:	n/a	n/a
43	ATF2	chr1:61798470-61798875	GM12878	blood:	n/a	n/a
44	ATF2	chr1:61803601-61804200	H1-hESC	embryonic stem cell:	n/a	n/a
45	ATF2	chr1:62107397-62107804	H1-hESC	embryonic stem cell:	n/a	n/a
46	ATF2	chr1:61797771-61798344	GM12878	blood:	n/a	n/a
47	ATF2	chr1:61797740-61798369	GM12878	blood:	n/a	n/a
48	ATF2	chr1:61984775-61985112	GM12878	blood:	n/a	n/a
49	ATF2	chr1:61798512-61798886	GM12878	blood:	n/a	n/a
50	ATF2	chr1:61749881-61750360	H1-hESC	embryonic stem cell:	n/a	n/a

(count:1344 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:61913481-61913531	LNCaP	prostate:	n/a
2	chr1:61948305-61948355	AG10803	skin:	n/a
3	chr1:61913481-61913531	LNCaP	prostate:	n/a
4	chr1:61948305-61948355	AG10803	skin:	n/a
5	chr1:61869782-61869832	A549	lung:	n/a
6	chr1:61886560-61886610	Jurkat	blood:	n/a
7	chr1:61925875-61925925	HL-60	blood:	n/a
8	chr1:61913481-61913531	HRPEpiC	eye:	n/a
9	chr1:61785870-61785920	GM12878	blood:	n/a
10	chr1:62102363-62102413	LNCaP	prostate:	n/a
11	chr1:61902105-61902155	IMR90	lung:	fetal
12	chr1:61785870-61785920	HPAEpiC	pulmonary alveolar:	n/a
13	chr1:62102363-62102413	HRCEpiC	kidney:	n/a
14	chr1:61886560-61886610	RPTEC	kidney:	n/a
15	chr1:61784017-61784067	AG09319	gingival:	n/a
16	chr1:62107542-62107592	HL-60	blood:	n/a
17	chr1:61869782-61869832	GM12878	blood:	n/a
18	chr1:61715231-61715281	SK-N-SH_RA	brain:	n/a
19	chr1:61925875-61925925	ovcar-3	ovarian:	n/a
20	chr1:62107542-62107592	AG04449	skin:	fetal
21	chr1:61843430-61843480	Caco-2	colon:	n/a
22	chr1:61715231-61715281	NT2-D1	testis:	n/a
23	chr1:61925875-61925925	HMEC	breast:	n/a
24	chr1:62107542-62107592	A549	lung:	n/a
25	chr1:61848996-61849046	MCF10A-Er-Src	breast:	n/a
26	chr1:62054902-62054952	HUVEC	blood vessel:	n/a
27	chr1:61750543-61750593	AG10803	skin:	n/a
28	chr1:62107430-62107480	PFSK-1	brain:	n/a
29	chr1:62107624-62107674	AG04449	skin:	fetal
30	chr1:62107430-62107480	T-47D	breast:	n/a
31	chr1:62107477-62107527	NHDF-neo	bronchial:	n/a
32	chr1:62102363-62102413	HAEpiC	amniotic membrane:	n/a
33	chr1:62107542-62107592	HMEC	breast:	n/a
34	chr1:62107542-62107592	GM12892	blood:	n/a
35	chr1:61803736-61803786	T-47D	breast:	n/a
36	chr1:61750543-61750593	Jurkat	blood:	n/a
37	chr1:62107430-62107480	HMEC	breast:	n/a
38	chr1:62107430-62107480	AG04450	lung:	fetal
39	chr1:61913481-61913531	HMEC	breast:	n/a
40	chr1:62005072-62005122	Jurkat	blood:	n/a
41	chr1:61848996-61849046	Jurkat	blood:	n/a
42	chr1:62054902-62054952	NB4	blood:	n/a
43	chr1:62107542-62107592	HEK293	kidney:	embryo
44	chr1:61902105-61902155	AG09309	skin:	n/a
45	chr1:62102363-62102413	HCPEpiC	choroid plexus:	n/a
46	chr1:62005072-62005122	AG04450	lung:	fetal
47	chr1:61925875-61925925	AG09319	gingival:	n/a
48	chr1:61913481-61913531	SAEC	small airway:	n/a
49	chr1:61908589-61908639	MCF10A-Er-Src	breast:	n/a
50	chr1:62005072-62005122	AG04449	skin:	fetal

(count:230 , 50 per page) page: 1 2 3 4 5

No.	Distal block	Cell Line	Cell type
1	chr1:61869340..61871337-chr1:61871668..61874296,2	K562	blood:
2	chr1:61821605..61823467-chr1:61848525..61850991,2	K562	blood:
3	chr1:61709999..61711668-chr1:61722903..61725455,2	K562	blood:
4	chr1:61802472..61805415-chr1:61917120..61919669,2	MCF-7	breast:
5	chr1:61731996..61734733-chr1:61736791..61738514,3	MCF-7	breast:
6	chr1:61908598..61910264-chr1:61911011..61913246,2	MCF-7	breast:
7	chr1:61821605..61824601-chr1:61847526..61850025,2	K562	blood:
8	chr1:61809086..61811561-chr1:61812317..61815281,2	K562	blood:
9	chr1:61788026..61790559-chr1:61794700..61796416,2	MCF-7	breast:
10	chr1:61701605..61703264-chr1:61789061..61791484,2	K562	blood:
11	chr1:61805404..61807718-chr1:61819195..61821796,2	K562	blood:
12	chr1:61957656..61960051-chr1:61961618..61963243,2	MCF-7	breast:
13	chr1:61916094..61917673-chr1:61919689..61921431,2	K562	blood:
14	chr1:61681230..61681758-chr1:61961831..61962532,2	MCF-7	breast:
15	chr1:61809209..61811913-chr1:61823172..61825226,2	K562	blood:
16	chr1:61949657..61951267-chr1:62070841..62073527,2	K562	blood:
17	chr1:61869340..61871337-chr1:61871668..61874296,2	K562	blood:
18	chr1:61515614..61516154-chr1:61918841..61919600,2	MCF-7	breast:
19	chr1:61635026..61638117-chr1:61715287..61717376,3	K562	blood:
20	chr1:61999747..62002930-chr1:62002962..62005689,3	K562	blood:
21	chr1:61721383..61724143-chr1:61726240..61729085,2	K562	blood:
22	chr1:61518677..61520785-chr1:61719829..61722787,3	K562	blood:
23	chr1:61999747..62002105-chr1:62002962..62005152,2	K562	blood:
24	chr1:61918678..61921342-chr1:61921885..61923902,2	MCF-7	breast:
25	chr1:61926467..61929109-chr1:61931369..61932898,2	K562	blood:
26	chr1:61784481..61786407-chr1:61788060..61789976,3	K562	blood:
27	chr1:61724468..61727373-chr1:61734110..61737676,4	K562	blood:
28	chr1:61486836..61488596-chr1:61734014..61735747,2	K562	blood:
29	chr1:61721383..61724143-chr1:61726240..61729085,2	K562	blood:
30	chr1:61747978..61751350-chr1:61752368..61755124,4	K562	blood:
31	chr1:61759273..61761992-chr1:61764171..61766892,3	MCF-7	breast:
32	chr1:61744927..61747648-chr1:61751228..61753700,3	K562	blood:
33	chr1:61605602..61607167-chr1:61748089..61750819,2	K562	blood:
34	chr1:61737048..61738584-chr1:61739343..61741335,2	K562	blood:
35	chr1:61748114..61750879-chr1:61800546..61802249,2	K562	blood:
36	chr1:61784481..61786407-chr1:61788060..61789976,3	K562	blood:
37	chr1:61705176..61707440-chr1:61708242..61713126,6	K562	blood:
38	chr1:61815681..61817818-chr1:61903758..61906179,2	K562	blood:
39	chr1:61719045..61721063-chr1:61723839..61725517,2	K562	blood:
40	chr1:61986285..61987971-chr1:61989372..61991361,2	K562	blood:
41	chr1:61957656..61960051-chr1:61961618..61963243,2	MCF-7	breast:
42	chr1:61670954..61672679-chr1:61702027..61704538,2	K562	blood:
43	chr1:61910005..61912784-chr1:61916999..61919026,2	MCF-7	breast:
44	chr1:61803556..61804528-chr1:61918731..61919655,3	MCF-7	breast:
45	chr1:61755399..61757717-chr1:61760353..61762667,2	K562	blood:
46	chr1:61716395..61718600-chr1:61728378..61730770,2	K562	blood:
47	chr1:61648753..61651711-chr1:61715272..61717636,2	K562	blood:
48	chr1:61772659..61774217-chr1:61790791..61792437,2	K562	blood:
49	chr1:62020528..62023253-chr1:62026530..62029145,2	MCF-7	breast:
50	chr1:61888820..61891280-chr1:61891861..61894353,3	K562	blood:

(count:23 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TM2D1-1	chr1:61714617-61714781	ENSG00000237853.1
2	lnc-TM2D1-1	chr1:61719083-61719184	NONHSAT003602
3	lnc-TM2D1-1	chr1:61716957-61717041	NR_104180
4	lnc-TM2D1-1	chr1:61716957-61717041	ENSG00000237853.1
5	lnc-INADL-1	chr1:62113728-62113990	XLOC_000227
6	lnc-INADL-6	chr1:61760224-61764056	NONHSAT003604
7	lnc-INADL-1	chr1:62102824-62102980	XLOC_000227
8	lnc-TM2D1-1	chr1:61719083-61719182	ENSG00000237853.1
9	lnc-TM2D1-1	chr1:61716957-61717041	NONHSAT003602
10	lnc-TM2D1-1	chr1:61714617-61714781	NR_104180
11	lnc-TM2D1-1	chr1:61715620-61715653	NR_104180
12	lnc-TM2D1-1	chr1:61714668-61714781	ENSG00000237853.2
13	lnc-TM2D1-1	chr1:61714666-61714781	NONHSAT003602
14	lnc-TM2D1-5	chr1:62019052-62019252	NONHSAT003606
15	lnc-TM2D1-1	chr1:61716957-61717041	ENSG00000237853.2
16	lnc-TM2D1-1	chr1:61714666-61714781	ENSG00000237853.2
17	lnc-TM2D1-1	chr1:61715620-61715653	ENSG00000237853.1
18	lnc-TM2D1-1	chr1:61719083-61719182	ENSG00000237853.2
19	lnc-TM2D1-1	chr1:61716957-61717041	ENSG00000237853.2
20	lnc-TM2D1-5	chr1:62021434-62021570	NONHSAT003606
21	lnc-TM2D1-1	chr1:61719083-61719182	ENSG00000237853.2
22	lnc-TM2D1-1	chr1:61715620-61715800	ENSG00000237853.2
23	lnc-TM2D1-1	chr1:61719083-61719190	NR_104180

No data

(count:7 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	NFIA	hsa-miR-107	chr1:61921698-61921705
2	NFIA	hsa-miR-107	chr1:61921685-61921705
3	NFIA	hsa-miR-107	chr1:61923191-61923197
4	NFIA	hsa-miR-124-3p	chr1:61922933-61922939
5	NFIA	hsa-miR-223-3p	chr1:61921788-61921810
6	NFIA	hsa-miR-223-3p	chr1:61921803-61921810
7	NFIA	hsa-miR-107	chr1:61923332-61923338

Variant related genes	Relation type
ENSG00000237853	TF binding region
ENSG00000223920	TF binding region
NFIA	TF binding region
ENSG00000264551	TF binding region
ENSG00000237853	CpG island
ENSG00000223920	CpG island
NFIA	CpG island
ENSG00000264551	CpG island
ENSG00000264551	chromatin interactions
ENSG00000132849	chromatin interactions
ENSG00000237853	chromatin interactions
ENSG00000271200	chromatin interactions
ENSG00000162599	chromatin interactions

Extended variants
information (count: 14655 )
Associated
traits (count: 100 )

Variant overlapped rSNPs/rCNVs (count:14655 , 50 per page) page: 1 2 3 4 5 6 7 ... 294

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs79500827	chr1:61700516-61700517	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs185451018	chr1:61700524-61700525	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs74090345	chr1:61700530-61700531	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs529943292	chr1:61700557-61700558	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs143509103	chr1:61700667-61700668	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs147265558	chr1:61700677-61700678	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs530544912	chr1:61700695-61700696	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs551829458	chr1:61700717-61700718	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs190980965	chr1:61700773-61700774	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs377358668	chr1:61700792-61700793	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs534444985	chr1:61700857-61700858	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs183702862	chr1:61700861-61700862	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs188237665	chr1:61700872-61700873	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs568359400	chr1:61700930-61700931	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs377135753	chr1:61700936-61700937	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs192383442	chr1:61700950-61700951	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs557643953	chr1:61701000-61701001	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs183297635	chr1:61701016-61701017	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs539841529	chr1:61701052-61701053	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs12565984	chr1:61701092-61701093	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs532784965	chr1:61701121-61701122	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs547361278	chr1:61701135-61701136	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs200048964	chr1:61701136-61701137	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs59459166	chr1:61701178-61701179	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs150522308	chr1:61701179-61701180	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs201255120	chr1:61701181-61701182	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs199625522	chr1:61701182-61701183	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs59346410	chr1:61701186-61701187	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs58359002	chr1:61701188-61701189	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs201915319	chr1:61701189-61701190	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs200539366	chr1:61701197-61701198	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs35824623	chr1:61701201-61701202	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs540777449	chr1:61701217-61701218	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs559544170	chr1:61701235-61701236	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs112917934	chr1:61701354-61701355	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs143098496	chr1:61701399-61701400	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs563625052	chr1:61701425-61701426	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs377460524	chr1:61701485-61701486	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs199585835	chr1:61701498-61701499	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs146112346	chr1:61701500-61701501	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs552684398	chr1:61701607-61701608	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs535848258	chr1:61701644-61701645	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs186920430	chr1:61701677-61701678	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs373811711	chr1:61701736-61701737	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs140142368	chr1:61701758-61701759	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs191396292	chr1:61701801-61701802	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs569378865	chr1:61701806-61701807	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs546292047	chr1:61701827-61701828	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs568519962	chr1:61701838-61701839	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs371231689	chr1:61701846-61701847	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:100)

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
Pancreatic cancer	17952125	CNVD
Medullary thyroid carcinoma	18765511	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Bipolar disorder	19114987	CNVD

Chromatin state (count:6664 , 50 per page) page: 1 2 3 4 5 6 7 ... 134

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:61680000-61720200	Weak transcription	Fetal Muscle Trunk	muscle
2	chr1:61682000-61706800	Weak transcription	Gastric	stomach
3	chr1:61692600-61703400	Weak transcription	H9 Cell Line	embryonic stem cell
4	chr1:61692800-61706800	Weak transcription	Fetal Lung	lung
5	chr1:61692800-61707000	Weak transcription	Fetal Stomach	stomach
6	chr1:61692800-61707200	Weak transcription	Pancreas	Pancrea
7	chr1:61693000-61704000	Weak transcription	Right Atrium	heart
8	chr1:61693000-61706800	Weak transcription	Brain Angular Gyrus	brain
9	chr1:61693000-61706800	Weak transcription	Fetal Muscle Leg	muscle
10	chr1:61694000-61706800	Weak transcription	Rectal Smooth Muscle	rectum
11	chr1:61694200-61703200	Weak transcription	Skeletal Muscle Male	skeletal muscle
12	chr1:61694200-61703200	Weak transcription	HMEC	breast
13	chr1:61694200-61703400	Weak transcription	Cortex derived primary cultured neurospheres	brain
14	chr1:61694200-61703600	Weak transcription	Brain Germinal Matrix	brain
15	chr1:61694200-61706800	Weak transcription	Adipose Nuclei	Adipose
16	chr1:61694200-61707000	Weak transcription	Brain Inferior Temporal Lobe	brain
17	chr1:61694400-61703600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
18	chr1:61696400-61703200	Weak transcription	A549	lung
19	chr1:61696600-61701600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
20	chr1:61696600-61701600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
21	chr1:61696600-61703200	Weak transcription	Brain Substantia Nigra	brain
22	chr1:61696600-61706800	Weak transcription	Right Ventricle	heart
23	chr1:61696600-61707200	Weak transcription	Left Ventricle	heart
24	chr1:61696800-61701600	Weak transcription	HUES6 Cell Line	embryonic stem cell
25	chr1:61696800-61707000	Weak transcription	Duodenum Smooth Muscle	Duodenum
26	chr1:61696800-61707200	Weak transcription	Pancreatic Islets	Pancreatic Islet
27	chr1:61696800-61707200	Weak transcription	Small Intestine	intestine
28	chr1:61697000-61701600	Weak transcription	Fetal Heart	heart
29	chr1:61697800-61700800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
30	chr1:61699000-61700800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
31	chr1:61699000-61703800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr1:61699200-61701600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
33	chr1:61699200-61701600	Weak transcription	H1 Cell Line	embryonic stem cell
34	chr1:61699200-61701600	Weak transcription	HUES48 Cell Line	embryonic stem cell
35	chr1:61699200-61703400	Weak transcription	Fetal Kidney	kidney
36	chr1:61699400-61703200	Weak transcription	Liver	Liver
37	chr1:61699400-61706800	Weak transcription	HepG2	liver
38	chr1:61699600-61700800	Enhancers	Primary hematopoietic stem cells	blood
39	chr1:61699600-61703600	Weak transcription	Brain Anterior Caudate	brain
40	chr1:61699600-61703600	Weak transcription	Brain Hippocampus Middle	brain
41	chr1:61699600-61704000	Enhancers	K562	blood
42	chr1:61700200-61700600	Enhancers	HUES64 Cell Line	embryonic stem cell
43	chr1:61700200-61700600	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
44	chr1:61700200-61700800	Enhancers	Brain Cingulate Gyrus	brain
45	chr1:61700400-61700800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
46	chr1:61700600-61701600	Weak transcription	HUES64 Cell Line	embryonic stem cell
47	chr1:61700600-61701600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
48	chr1:61700600-61703600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
49	chr1:61700800-61701400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
50	chr1:61700800-61703600	Weak transcription	Brain Cingulate Gyrus	brain

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