Variant report

Variant	nsv1004608
Chromosome Location	chr1:144949963-145113854
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:5673)
CpG islands
(count:4211)
Chromatin interactive
region (count:351)
LncRNA
region (count:12)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:5673 , 50 per page) page: 1 2 3 4 5 6 7 ... 114

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:145083440-145084471	K562	blood:	n/a	n/a
2	ARID3A	chr1:145000157-145004850	K562	blood:	n/a	chr1:145001553-145001569 chr1:145004748-145004764
3	ARID3A	chr1:144997084-144999662	K562	blood:	n/a	n/a
4	ARID3A	chr1:144988785-144990011	HepG2	liver:	n/a	n/a
5	ARID3A	chr1:145061354-145062417	K562	blood:	n/a	n/a
6	ARID3A	chr1:145098092-145098776	HepG2	liver:	n/a	n/a
7	ARID3A	chr1:145040639-145043538	K562	blood:	n/a	n/a
8	ARID3A	chr1:145039806-145040082	HepG2	liver:	n/a	n/a
9	ARID3A	chr1:145054062-145056297	K562	blood:	n/a	chr1:145054435-145054451 chr1:145054273-145054289 chr1:145054272-145054288 chr1:145054436-145054452
10	ARID3A	chr1:144991522-144993662	K562	blood:	n/a	n/a
11	ARID3A	chr1:145012025-145018939	K562	blood:	n/a	chr1:145012568-145012584 chr1:145012567-145012583
12	ARID3A	chr1:145014466-145014972	HepG2	liver:	n/a	n/a
13	ARID3A	chr1:145027372-145031947	K562	blood:	n/a	n/a
14	ARID3A	chr1:145058588-145061058	K562	blood:	n/a	n/a
15	ARID3A	chr1:144994237-144996744	K562	blood:	n/a	n/a
16	ARID3A	chr1:145005457-145007401	K562	blood:	n/a	n/a
17	ARID3A	chr1:145023275-145025964	K562	blood:	n/a	n/a
18	ARID3A	chr1:145040051-145040226	K562	blood:	n/a	n/a
19	ARID3A	chr1:145096149-145096769	HepG2	liver:	n/a	n/a
20	ARID3A	chr1:145091964-145092746	HepG2	liver:	n/a	n/a
21	ARID3A	chr1:145089768-145090509	K562	blood:	n/a	n/a
22	ARID3A	chr1:145007845-145011203	K562	blood:	n/a	n/a
23	ARID3A	chr1:144989106-144991213	K562	blood:	n/a	n/a
24	ATF1	chr1:145107917-145107980	K562	blood:	n/a	n/a
25	ATF1	chr1:145029752-145031659	K562	blood:	n/a	n/a
26	ATF1	chr1:144997529-144998431	K562	blood:	n/a	n/a
27	ATF1	chr1:145090189-145090575	K562	blood:	n/a	n/a
28	ATF1	chr1:145070839-145072121	K562	blood:	n/a	n/a
29	ATF1	chr1:145083579-145084451	K562	blood:	n/a	n/a
30	ATF1	chr1:145074748-145075398	K562	blood:	n/a	n/a
31	ATF1	chr1:145054709-145055914	K562	blood:	n/a	n/a
32	ATF1	chr1:145080812-145081067	K562	blood:	n/a	n/a
33	ATF1	chr1:145112421-145113298	K562	blood:	n/a	n/a
34	ATF1	chr1:145018078-145018857	K562	blood:	n/a	n/a
35	ATF1	chr1:145001703-145004761	K562	blood:	n/a	n/a
36	ATF1	chr1:145069602-145070170	K562	blood:	n/a	n/a
37	ATF1	chr1:145078844-145078995	K562	blood:	n/a	n/a
38	ATF1	chr1:144994316-144996366	K562	blood:	n/a	n/a
39	ATF1	chr1:144991677-144992162	K562	blood:	n/a	n/a
40	ATF1	chr1:145086819-145087312	K562	blood:	n/a	n/a
41	ATF1	chr1:145077527-145078634	K562	blood:	n/a	n/a
42	ATF1	chr1:145082093-145082887	K562	blood:	n/a	n/a
43	ATF1	chr1:144988840-144990055	K562	blood:	n/a	n/a
44	ATF1	chr1:144998715-144999351	K562	blood:	n/a	n/a
45	ATF1	chr1:145037166-145037364	K562	blood:	n/a	n/a
46	ATF1	chr1:145032820-145034366	K562	blood:	n/a	n/a
47	ATF1	chr1:145108235-145108438	K562	blood:	n/a	n/a
48	ATF1	chr1:145111322-145111864	K562	blood:	n/a	n/a
49	ATF1	chr1:145073353-145074236	K562	blood:	n/a	n/a
50	ATF1	chr1:145014382-145016089	K562	blood:	n/a	n/a

(count:4211 , 50 per page) page: 1 2 3 4 5 6 7 ... 85

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:145013480-145013530	HepG2	liver:	n/a
2	chr1:145039741-145039791	HCT-116	colon:	n/a
3	chr1:145013480-145013530	HepG2	liver:	n/a
4	chr1:145039741-145039791	HCT-116	colon:	n/a
5	chr1:145096479-145096529	Hela-S3	cervix:	n/a
6	chr1:145075538-145075588	AG04450	lung:	fetal
7	chr1:145077772-145077822	PrEC	prostate:	n/a
8	chr1:145100564-145100614	Hela-S3	cervix:	n/a
9	chr1:144995889-144995939	H1-hESC	embryonic stem cell:	embryo
10	chr1:145042811-145042861	Jurkat	blood:	n/a
11	chr1:145076221-145076271	HUVEC	blood vessel:	n/a
12	chr1:145075831-145075881	H1-hESC	embryonic stem cell:	embryo
13	chr1:145089017-145089067	AG09309	skin:	n/a
14	chr1:145028465-145028515	AoSMC	blood vessel:	n/a
15	chr1:145075349-145075399	HL-60	blood:	n/a
16	chr1:145059467-145059517	HRCEpiC	kidney:	n/a
17	chr1:145054779-145054829	Hepatocyte	liver:	n/a
18	chr1:144994715-144994765	PrEC	prostate:	n/a
19	chr1:145036025-145036075	HPAEpiC	pulmonary alveolar:	n/a
20	chr1:145073743-145073793	GM12878	blood:	n/a
21	chr1:145097220-145097270	Hela-S3	cervix:	n/a
22	chr1:144952173-144952223	LNCaP	prostate:	n/a
23	chr1:144994715-144994765	GM06990	blood:	n/a
24	chr1:144994318-144994368	HL-60	blood:	n/a
25	chr1:145092330-145092380	HRCEpiC	kidney:	n/a
26	chr1:145015987-145016037	MCF10A-Er-Src	breast:	n/a
27	chr1:145036025-145036075	NHBE	bronchial:	n/a
28	chr1:145089017-145089067	HepG2	liver:	n/a
29	chr1:145092330-145092380	Caco-2	colon:	n/a
30	chr1:145092576-145092626	Caco-2	colon:	n/a
31	chr1:145035112-145035162	PFSK-1	brain:	n/a
32	chr1:145072507-145072557	AoSMC	blood vessel:	n/a
33	chr1:145096403-145096453	CMK	blood:	n/a
34	chr1:145097220-145097270	GM12891	blood:	n/a
35	chr1:145040160-145040210	MCF10A-Er-Src	breast:	n/a
36	chr1:145040160-145040210	HNPCEpiC	eye:	n/a
37	chr1:144998869-144998919	U87	brain:	n/a
38	chr1:145104707-145104757	HepG2	liver:	n/a
39	chr1:145079447-145079497	PANC-1	pancreas:	n/a
40	chr1:145096125-145096175	HCM	heart:	n/a
41	chr1:145054779-145054829	K562	blood:	n/a
42	chr1:145100564-145100614	MCF10A-Er-Src	breast:	n/a
43	chr1:145096567-145096617	LNCaP	prostate:	n/a
44	chr1:145028465-145028515	HEEpiC	esophagus:	n/a
45	chr1:144995889-144995939	PFSK-1	brain:	n/a
46	chr1:144995889-144995939	U87	brain:	n/a
47	chr1:145075538-145075588	NHDF-neo	bronchial:	n/a
48	chr1:145004468-145004518	HEK293	kidney:	embryo
49	chr1:145039929-145039979	AG10803	skin:	n/a
50	chr1:145039893-145039943	Caco-2	colon:	n/a

(count:351 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Distal block	Cell Line	Cell type
1	chr1:145073942..145076773-chr1:145095058..145097883,2	K562	blood:
2	chr1:145069991..145072792-chr1:145078438..145080718,2	K562	blood:
3	chr1:144992633..144993235-chr1:145029941..145030565,2	MCF-7	breast:
4	chr1:145041571..145043626-chr1:145061448..145065159,3	K562	blood:
5	chr1:145007566..145009681-chr1:145060269..145062517,2	K562	blood:
6	chr1:144532285..144535839-chr1:144994993..144998864,6	K562	blood:
7	chr1:145070476..145072137-chr10:116063962..116066541,2	MCF-7	breast:
8	chr1:144988330..144990331-chr1:145096274..145097862,2	MCF-7	breast:
9	chr1:145082670..145085511-chr1:145092846..145095216,2	MCF-7	breast:
10	chr1:144997738..145000659-chr1:145007857..145011011,3	MCF-7	breast:
11	chr1:145002712..145004491-chr1:145095156..145096973,2	MCF-7	breast:
12	chr1:145056819..145059219-chr1:145060207..145063114,3	K562	blood:
13	chr1:145107602..145109757-chr1:145381655..145383784,3	MCF-7	breast:
14	chr1:144988088..144989012-chr1:145058100..145059991,5	MCF-7	breast:
15	chr1:145082537..145085433-chr1:145102296..145104665,3	MCF-7	breast:
16	chr1:145070825..145073370-chr1:145075606..145078023,2	K562	blood:
17	chr1:145018409..145019163-chr1:145060589..145061400,2	MCF-7	breast:
18	chr1:144931832..144934351-chr1:145043528..145045220,3	K562	blood:
19	chr1:144934397..144936617-chr1:145058068..145059656,2	MCF-7	breast:
20	chr1:145028195..145030084-chr1:145108356..145110933,3	K562	blood:
21	chr1:120480674..120483081-chr1:145098868..145100829,2	MCF-7	breast:
22	chr1:145069551..145072010-chr1:145087296..145089112,2	K562	blood:
23	chr1:144932512..144934807-chr1:144998183..145000518,2	MCF-7	breast:
24	chr1:145068824..145071051-chr1:145086179..145089112,2	K562	blood:
25	chr1:145013051..145015770-chr1:145381611..145384530,4	K562	blood:
26	chr1:144532567..144534443-chr1:145045258..145048893,3	K562	blood:
27	chr1:144995928..144998719-chr1:145383813..145386385,2	K562	blood:
28	chr1:144993668..144997286-chr1:145038559..145041171,3	MCF-7	breast:
29	chr1:144993800..144995715-chr1:145096861..145099755,2	K562	blood:
30	chr1:144534936..144535880-chr1:145058706..145059612,4	MCF-7	breast:
31	chr1:144999924..145002233-chr6:21588409..21590209,2	MCF-7	breast:
32	chr1:144932519..144933068-chr1:144989004..144989890,2	MCF-7	breast:
33	chr1:145096683..145099291-chr17:57931322..57933303,2	MCF-7	breast:
34	chr1:144988330..144990331-chr1:145096274..145097862,2	MCF-7	breast:
35	chr1:144917481..144919146-chr1:145058283..145060040,20	MCF-7	breast:
36	chr1:145016166..145017682-chr1:145058594..145060560,2	K562	blood:
37	chr1:144989112..144989905-chr1:145061477..145061994,2	MCF-7	breast:
38	chr1:145057641..145059158-chr1:145100599..145102878,2	MCF-7	breast:
39	chr1:145028195..145030084-chr1:145108356..145110933,3	K562	blood:
40	chr1:145032581..145034474-chr1:145068467..145071383,2	MCF-7	breast:
41	chr1:145056819..145059219-chr1:145060207..145063114,3	K562	blood:
42	chr1:145009595..145012188-chr1:145012261..145014678,3	MCF-7	breast:
43	chr1:144930866..144933492-chr1:145054484..145057318,3	MCF-7	breast:
44	chr1:144534036..144535735-chr1:145018265..145020000,2	K562	blood:
45	chr1:145014159..145015000-chr1:145060710..145062762,6	MCF-7	breast:
46	chr1:144931917..144932538-chr1:144989172..144989676,2	MCF-7	breast:
47	chr1:145054096..145056410-chr1:147805245..147807903,2	K562	blood:
48	chr1:145021531..145024475-chr1:145100250..145102590,2	K562	blood:
49	chr1:145024379..145028035-chr1:145095540..145100170,5	K562	blood:
50	chr1:145023266..145026073-chr1:145059016..145061272,2	MCF-7	breast:

(count:12 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-POLR3GL-6	chr1:145021112-145021167	NONHSAT005872
2	lnc-NBPF9-3	chr1:145004781-145005286	NONHSAT005869
3	lnc-POLR3GL-6	chr1:145017881-145017999	NONHSAT005872
4	lnc-NBPF9-5	chr1:145018395-145018959	ENSG00000272755.1
5	lnc-POLR3GL-6	chr1:145015873-145016011	NONHSAT005872
6	lnc-NOTCH2NL-3	chr1:145112627-145113408	ucscGeneNc_uc001epf_1
7	lnc-PDE4DIP-5	chr1:145088039-145088567	NONHSAT005874
8	lnc-NBPF9-4	chr1:145013726-145013828	NONHSAT005870
9	lnc-POLR3GL-6	chr1:145039590-145039851	NONHSAT005872
10	lnc-NOTCH2NL-3	chr1:145110974-145111762	ucscGeneNc_uc001epf_1
11	lnc-NOTCH2NL-4	chr1:145044651-145044900	NONHSAT005873
12	lnc-NBPF9-4	chr1:145016388-145016968	NONHSAT005870

No data

Variant related genes	Relation type
SEC22B	TF binding region
RN7SKP88	TF binding region
ENSG00000272755	TF binding region
PDE4DIP	TF binding region
ENSG00000271546	TF binding region
ENSG00000268172	TF binding region
SEC22B	CpG island
RN7SKP88	CpG island
ENSG00000272755	CpG island
PDE4DIP	CpG island
ENSG00000271546	CpG island
ENSG00000268172	CpG island
ENSG00000174827	chromatin interactions
ENSG00000160972	chromatin interactions
ENSG00000184260	chromatin interactions
ENSG00000261139	chromatin interactions
ENSG00000188486	chromatin interactions
ENSG00000115919	chromatin interactions
ENSG00000212694	chromatin interactions
ENSG00000120137	chromatin interactions
ENSG00000203843	chromatin interactions
ENSG00000223380	chromatin interactions
ENSG00000158417	chromatin interactions
ENSG00000239335	chromatin interactions
ENSG00000252656	chromatin interactions
ENSG00000201699	chromatin interactions
ENSG00000139725	chromatin interactions
ENSG00000233396	chromatin interactions
ENSG00000079335	chromatin interactions
ENSG00000202408	chromatin interactions
ENSG00000171735	chromatin interactions
ENSG00000139233	chromatin interactions
ENSG00000167904	chromatin interactions
ENSG00000271546	chromatin interactions
ENSG00000268172	chromatin interactions
ENSG00000115514	chromatin interactions
ENSG00000223491	chromatin interactions
ENSG00000239306	chromatin interactions
ENSG00000255182	chromatin interactions
ENSG00000180370	chromatin interactions
ENSG00000184678	chromatin interactions
ENSG00000248643	chromatin interactions
ENSG00000237436	chromatin interactions
ENSG00000226446	chromatin interactions
ENSG00000169129	chromatin interactions
ENSG00000206737	chromatin interactions
ENSG00000137574	chromatin interactions
ENSG00000225362	chromatin interactions
ENSG00000178104	chromatin interactions
ENSG00000125347	chromatin interactions
ENSG00000201558	chromatin interactions
SMAD7	miRNA target sites
NSMAF	miRNA target sites

Extended variants
information (count: 6546 )
Associated
traits (count: 181 )

Variant overlapped rSNPs/rCNVs (count:6546 , 50 per page) page: 1 2 3 4 5 6 7 ... 131

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs60370016	chr1:144949971-144949972	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs587704373	chr1:144949981-144949982	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs587604881	chr1:144949998-144949999	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs587681392	chr1:144950032-144950033	Weak transcription Strong transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs540005	chr1:144950044-144950045	Weak transcription Strong transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs587714268	chr1:144950080-144950081	Weak transcription Strong transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs587605694	chr1:144950115-144950116	Weak transcription Strong transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs370543317	chr1:144950139-144950140	Weak transcription Strong transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs55959508	chr1:144950140-144950141	Weak transcription Strong transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs587666718	chr1:144950156-144950157	Weak transcription Strong transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs11581717	chr1:144950171-144950172	Weak transcription Strong transcription Active TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs538325	chr1:144950190-144950191	Weak transcription Strong transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs201535829	chr1:144950193-144950194	Weak transcription Strong transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs587619721	chr1:144950199-144950200	Weak transcription Strong transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs587696718	chr1:144950242-144950243	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs201720633	chr1:144950256-144950257	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs28403871	chr1:144950262-144950263	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs2863337	chr1:144950265-144950266	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs587648155	chr1:144950300-144950301	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs587705264	chr1:144950308-144950309	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs375377964	chr1:144950326-144950327	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs587610023	chr1:144950407-144950408	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs112871837	chr1:144950456-144950457	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs55908078	chr1:144950506-144950507	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs587744607	chr1:144950557-144950558	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs587646619	chr1:144950608-144950609	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs587726561	chr1:144950624-144950625	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs141008325	chr1:144950649-144950650	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs150210191	chr1:144950711-144950712	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs112520540	chr1:144950755-144950756	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs55990332	chr1:144950772-144950773	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs587760048	chr1:144950783-144950784	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs587656953	chr1:144950813-144950814	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs587712425	chr1:144950822-144950823	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs587610517	chr1:144950839-144950840	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs633711	chr1:144950873-144950874	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs633385	chr1:144950904-144950905	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs4649708	chr1:144950912-144950913	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs2762730	chr1:144950925-144950926	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs7548238	chr1:144950969-144950970	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs3124679	chr1:144950998-144950999	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs587657854	chr1:144951053-144951054	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs622753	chr1:144951057-144951058	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs587720933	chr1:144951062-144951063	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs183650315	chr1:144951093-144951094	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs3855994	chr1:144951112-144951113	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs1663973	chr1:144951128-144951129	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs201726768	chr1:144951130-144951131	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs587694952	chr1:144951155-144951156	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs200440041	chr1:144951177-144951178	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:181)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Cancer	21129771	CNVD
Non-small cell lung cancer	21385341	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
Ewing''s sarcoma	21437220	CNVD
Liposarcoma	21253554	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Breast cancer	20409316	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	21183584	CNVD
Multiple myeloma	16461302	CNVD
Lung cancer	18438408	CNVD
Rett syndrome	21593744	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Systemic lupus erythematosus	21956041	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
small cell lung cancer	20016488	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Non-small cell lung cancer	21829676	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Neuroblastoma	21899760	CNVD
Breast cancer	17899364	CNVD
Bladder cancer	19088036	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21611746	CNVD
Retinoblastoma	19183342	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21990379	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	22499536	CNVD
Schizophrenia	18923514	CNVD
Neuroblastoma	21124317	CNVD
Autism	20970697	CNVD
Bipolar disorder	19114987	CNVD
Epilepsy	20970697	CNVD
Schizophrenia	22118685	CNVD
Schizophrenia	20587603	CNVD
Schizophrenia	21285140	CNVD
Schizophrenia	20553308	CNVD
Schizophrenia	21956041	CNVD
Schizophrenia	20970697	CNVD
Addison''s disease	21851588	CNVD
Heart disease	22199024	CNVD
Mental retardation	19951919	CNVD
Ovarian cancer	20844748	CNVD
Schizophrenia	21399695	CNVD
Prostate cancer	17217626	CNVD
Congenital heart defect	22199024	CNVD
TAR Syndrome	17847015	CNVD
Thrombocytopenia-absent radius syndrome	17236129	CNVD
Autism	18784092	CNVD
Congenital abnormalities	18784092	CNVD
Mental retardation	18784092	CNVD
Schizophrenia	19855392	CNVD
Ovarian cancer	22174824	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	19521722	CNVD
Mental retardation	19521722	CNVD
Schizophrenia	19521646	CNVD
Neuroblastoma	19536264	CNVD
Epilepsy	20923578	CNVD
Mental retardation	17124404	CNVD
Schizophrenia	19348701	CNVD
Schizophrenia	18668039	CNVD
Schizophrenia	19443537	CNVD
Schizophrenia	19571808	CNVD
Velocardiofacial syndrome	19329560	CNVD
Autism	19955444	CNVD
Autism	20964600	CNVD
Schizophrenia	19955444	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Colorectal cancer	20459617	CNVD
Osteosarcoma	19286668	CNVD
Osteosarcoma	17242211	CNVD
Ovarian cancer	17242211	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Schizophrenia	18990708	CNVD
Sudden cardiac death	19188705	CNVD
Plasma-cell dyscrasia	16705089	CNVD
Myeloma	17024118	CNVD
Cancer	17060936	CNVD
Multiple myeloma	16616336	CNVD
Type 2 diabetes	19141583	CNVD
Chordoma	18071362	CNVD
Hepatocellular carcinoma	18803288	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Urothelial carcinoma	21177765	CNVD
Burkitt''s lymphoma	19759907	CNVD
Breast cancer	17142309	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Follicular lymphoma	18703704	CNVD
Lung adenocarcinoma	17982442	CNVD
Breast cancer	21509527	CNVD
Tetralogy of Fallot	22912587	CNVD
Autism	18522746	CNVD
Bladder cancer	21909424	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Acute myeloid leukemia	20729466	CNVD
Schizophrenia	19197363	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Schizophrenia	23813976	CNVD
Lung adenocarcinoma	21935476	CNVD
idiopathic generalized epilepsy	19843651	CNVD
Schizophrenia	19843651	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD
Autism	20531469	CNVD
Autism	20858243	CNVD
Breast cancer	22522925	CNVD
Autism	22543975	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Epilepsy	20502679	CNVD
Autism	20841430	CNVD
Developmental delay	20808231	CNVD
Obesity	20808231	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Congenital anomalies of the kidney and urinary tract	20605837	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD

Chromatin state (count:7006 , 50 per page) page: 1 2 3 4 5 6 7 ... 141

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:144939800-144952200	Strong transcription	K562	blood
2	chr1:144941600-144950000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
3	chr1:144941600-144951000	Strong transcription	Left Ventricle	heart
4	chr1:144942200-144960200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
5	chr1:144942400-144951400	Strong transcription	Brain Cingulate Gyrus	brain
6	chr1:144942400-144952200	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
7	chr1:144942600-144952000	Strong transcription	Osteobl	bone
8	chr1:144942600-144952200	Strong transcription	Placenta	Placenta
9	chr1:144942800-144951800	Strong transcription	HSMM	muscle
10	chr1:144942800-144952200	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
11	chr1:144942800-144952200	Strong transcription	Muscle Satellite Cultured Cells	--
12	chr1:144942800-144952200	Strong transcription	HSMMtube	muscle
13	chr1:144943200-144953000	Weak transcription	Fetal Brain Female	brain
14	chr1:144943400-144961000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
15	chr1:144944000-144950000	Weak transcription	Fetal Stomach	stomach
16	chr1:144944000-144950000	Weak transcription	Sigmoid Colon	Sigmoid Colon
17	chr1:144944000-144950600	Weak transcription	Lung	lung
18	chr1:144944000-144966200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
19	chr1:144944200-144950000	Weak transcription	NHLF	lung
20	chr1:144945600-144950200	Strong transcription	Psoas Muscle	Psoas
21	chr1:144945800-144952200	Strong transcription	Adipose Nuclei	Adipose
22	chr1:144946600-144964800	Weak transcription	HMEC	breast
23	chr1:144946800-144950400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
24	chr1:144946800-144950800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
25	chr1:144946800-144962800	Weak transcription	Liver	Liver
26	chr1:144946800-144966200	Weak transcription	Duodenum Smooth Muscle	Duodenum
27	chr1:144947400-144952400	Strong transcription	Skeletal Muscle Male	skeletal muscle
28	chr1:144947400-144956400	Weak transcription	Stomach Smooth Muscle	stomach
29	chr1:144947400-144972800	Weak transcription	Right Ventricle	heart
30	chr1:144948400-144951600	Weak transcription	Fetal Brain Male	brain
31	chr1:144949000-144952200	Strong transcription	Skeletal Muscle Female	skeletal muscle
32	chr1:144949000-144964800	Weak transcription	Brain Angular Gyrus	brain
33	chr1:144949000-144964800	Weak transcription	Brain Hippocampus Middle	brain
34	chr1:144949000-144964800	Weak transcription	Brain Inferior Temporal Lobe	brain
35	chr1:144949200-144950200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
36	chr1:144949200-144950400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
37	chr1:144949200-144950400	Weak transcription	Fetal Heart	heart
38	chr1:144949200-144950800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
39	chr1:144949200-144950800	Weak transcription	Fetal Muscle Leg	muscle
40	chr1:144949200-144951200	Weak transcription	Fetal Muscle Trunk	muscle
41	chr1:144949200-144951400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
42	chr1:144949200-144953000	Weak transcription	NH-A	brain
43	chr1:144949200-144953600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
44	chr1:144949200-144954400	Weak transcription	GM12878-XiMat	blood
45	chr1:144949200-144954800	Weak transcription	NHDF-Ad	bronchial
46	chr1:144949200-144964800	Weak transcription	Brain Anterior Caudate	brain
47	chr1:144949200-144964800	Weak transcription	Brain Substantia Nigra	brain
48	chr1:144949200-144966200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
49	chr1:144949200-144966200	Weak transcription	Brain Germinal Matrix	brain
50	chr1:144949200-144972400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin

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