Variant report

Variant	nsv911954
Chromosome Location	chr19:43374601-43794586
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:5773)
CpG islands
(count:3051)
Chromatin interactive
region (count:6)
LncRNA
region (count:61)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:5773 , 50 per page) page: 1 2 3 4 5 6 7 ... 116

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr19:43779068-43779071	K562	blood:	n/a	n/a
2	ATF1	chr19:43733581-43733686	K562	blood:	n/a	n/a
3	ATF3	chr19:43686016-43686763	A549	lung:	n/a	n/a
4	BATF	chr19:43552186-43552537	GM12878	blood:	n/a	chr19:43552319-43552330
5	BATF	chr19:43552261-43552460	GM12878	blood:	n/a	chr19:43552319-43552330
6	BATF	chr19:43775309-43775522	GM12878	blood:	n/a	n/a
7	BATF	chr19:43613006-43613315	GM12878	blood:	n/a	chr19:43613110-43613121
8	BATF	chr19:43591924-43592150	GM12878	blood:	n/a	n/a
9	BATF	chr19:43711409-43711658	GM12878	blood:	n/a	n/a
10	BATF	chr19:43442962-43443231	GM12878	blood:	n/a	n/a
11	BATF	chr19:43738081-43738296	GM12878	blood:	n/a	chr19:43738185-43738196
12	BATF	chr19:43588401-43588710	GM12878	blood:	n/a	n/a
13	BATF	chr19:43692257-43692526	GM12878	blood:	n/a	n/a
14	BATF	chr19:43692397-43692675	GM12878	blood:	n/a	n/a
15	BCL3	chr19:43402518-43403428	A549	lung:	n/a	n/a
16	BHLHE40	chr19:43733601-43733620	K562	blood:	n/a	n/a
17	BHLHE40	chr19:43582147-43582203	K562	blood:	n/a	n/a
18	BHLHE40	chr19:43709323-43709343	K562	blood:	n/a	n/a
19	BHLHE40	chr19:43427453-43427512	GM12878	blood:	n/a	n/a
20	BHLHE40	chr19:43385480-43385517	K562	blood:	n/a	n/a
21	BRCA1	chr19:43436723-43436914	Hela-S3	cervix:	n/a	n/a
22	BRCA1	chr19:43624776-43624937	Hela-S3	cervix:	n/a	n/a
23	BRCA1	chr19:43525934-43526309	Hela-S3	cervix:	n/a	n/a
24	BRCA1	chr19:43769426-43769782	Hela-S3	cervix:	n/a	n/a
25	CBX3	chr19:43385431-43385838	K562	blood:	n/a	n/a
26	CBX3	chr19:43775261-43775711	HCT-116	colon:	n/a	n/a
27	CBX3	chr19:43775276-43775644	K562	blood:	n/a	n/a
28	CBX3	chr19:43385505-43385738	K562	blood:	n/a	n/a
29	CEBPB	chr19:43560474-43560633	A549	lung:	n/a	chr19:43560568-43560581 chr19:43560568-43560579 chr19:43560568-43560581
30	CEBPB	chr19:43564423-43564649	IMR90	lung:	n/a	n/a
31	CEBPB	chr19:43685962-43686735	A549	lung:	n/a	n/a
32	CEBPB	chr19:43618826-43619087	IMR90	lung:	n/a	n/a
33	CEBPB	chr19:43562943-43563108	MCF-7	breast:	n/a	n/a
34	CEBPB	chr19:43436540-43437331	IMR90	lung:	n/a	n/a
35	CEBPB	chr19:43510075-43510341	Hela-S3	cervix:	n/a	chr19:43510191-43510202
36	CEBPB	chr19:43496316-43496617	A549	lung:	n/a	n/a
37	CEBPB	chr19:43379145-43379767	IMR90	lung:	n/a	n/a
38	CEBPB	chr19:43379142-43379806	Hela-S3	cervix:	n/a	n/a
39	CEBPB	chr19:43403099-43403104	A549	lung:	n/a	n/a
40	CEBPB	chr19:43786125-43786327	Hela-S3	cervix:	n/a	n/a
41	CEBPB	chr19:43525813-43526656	Hela-S3	cervix:	n/a	n/a
42	CEBPB	chr19:43500870-43501012	IMR90	lung:	n/a	n/a
43	CEBPB	chr19:43436570-43436856	A549	lung:	n/a	n/a
44	CEBPB	chr19:43525800-43526621	IMR90	lung:	n/a	n/a
45	CEBPB	chr19:43496486-43496642	K562	blood:	n/a	n/a
46	CEBPB	chr19:43517268-43517468	HepG2	liver:	n/a	chr19:43517348-43517359
47	CEBPB	chr19:43685985-43686627	IMR90	lung:	n/a	n/a
48	CEBPB	chr19:43525986-43526150	A549	lung:	n/a	n/a
49	CEBPB	chr19:43573042-43573317	HepG2	liver:	n/a	chr19:43573163-43573174
50	CEBPB	chr19:43482706-43482918	Hela-S3	cervix:	n/a	n/a

(count:3051 , 50 per page) page: 1 2 3 4 5 6 7 ... 62

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:43531821-43531871	PFSK-1	brain:	n/a
2	chr19:43531821-43531871	PFSK-1	brain:	n/a
3	chr19:43691930-43691980	H1-hESC	embryonic stem cell:	embryo
4	chr19:43385100-43385150	IMR90	lung:	fetal
5	chr19:43588055-43588105	IMR90	lung:	fetal
6	chr19:43690996-43691046	HL-60	blood:	n/a
7	chr19:43421584-43421634	BJ	skin:	n/a
8	chr19:43384780-43384830	HRCEpiC	kidney:	n/a
9	chr19:43423119-43423169	HAEpiC	amniotic membrane:	n/a
10	chr19:43680072-43680122	HUVEC	blood vessel:	n/a
11	chr19:43410455-43410505	GM12891	blood:	n/a
12	chr19:43528994-43529044	HNPCEpiC	eye:	n/a
13	chr19:43774921-43774971	A549	lung:	n/a
14	chr19:43709754-43709804	HMEC	breast:	n/a
15	chr19:43442484-43442534	HRCEpiC	kidney:	n/a
16	chr19:43383799-43383849	SAEC	small airway:	n/a
17	chr19:43442804-43442854	GM12891	blood:	n/a
18	chr19:43423265-43423315	AG09309	skin:	n/a
19	chr19:43531770-43531820	NHBE	bronchial:	n/a
20	chr19:43711064-43711114	SKMC	muscle:	n/a
21	chr19:43442809-43442859	NH-A	brain:	n/a
22	chr19:43442804-43442854	LNCaP	prostate:	n/a
23	chr19:43588055-43588105	GM12878	blood:	n/a
24	chr19:43709832-43709882	HNPCEpiC	eye:	n/a
25	chr19:43588055-43588105	BE2_C	brain:	n/a
26	chr19:43680072-43680122	AG09309	skin:	n/a
27	chr19:43385047-43385097	PrEC	prostate:	n/a
28	chr19:43588069-43588119	GM12878	blood:	n/a
29	chr19:43410455-43410505	HRPEpiC	eye:	n/a
30	chr19:43588069-43588119	SK-N-MC	brain:	n/a
31	chr19:43530536-43530586	NT2-D1	testis:	n/a
32	chr19:43588055-43588105	HMEC	breast:	n/a
33	chr19:43385047-43385097	K562	blood:	n/a
34	chr19:43709832-43709882	Hela-S3	cervix:	n/a
35	chr19:43528994-43529044	BE2_C	brain:	n/a
36	chr19:43587500-43587550	HAEpiC	amniotic membrane:	n/a
37	chr19:43709654-43709704	HepG2	liver:	n/a
38	chr19:43423119-43423169	HCT-116	colon:	n/a
39	chr19:43683698-43683748	AG10803	skin:	n/a
40	chr19:43690996-43691046	HEK293	kidney:	embryo
41	chr19:43442809-43442859	AG04449	skin:	fetal
42	chr19:43423176-43423226	BJ	skin:	n/a
43	chr19:43709654-43709704	SK-N-MC	brain:	n/a
44	chr19:43441294-43441344	U87	brain:	n/a
45	chr19:43774921-43774971	HepG2	liver:	n/a
46	chr19:43709832-43709882	BJ	skin:	n/a
47	chr19:43673501-43673551	NHDF-neo	bronchial:	n/a
48	chr19:43421584-43421634	T-47D	breast:	n/a
49	chr19:43588069-43588119	H1-hESC	embryonic stem cell:	embryo
50	chr19:43421584-43421634	Hepatocyte	liver:	n/a

(count:6 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:43608137..43608719-chr19:43820621..43821519,2	MCF-7	breast:
2	chr19:43523469..43524084-chr19:43531918..43532440,2	MCF-7	breast:
3	chr19:43265768..43266290-chr19:43769932..43770473,2	MCF-7	breast:
4	chr19:43531581..43532101-chr2:1136088..1136613,2	MCF-7	breast:
5	chr19:43678340..43681333-chr19:43698109..43700078,2	MCF-7	breast:
6	chr19:43523469..43524084-chr19:43531918..43532440,2	MCF-7	breast:

(count:61 , 50 per page) page: 1 2

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PSG2-4	chr19:43521383-43521753	NONHSAT066578
2	lnc-PSG9-2	chr19:43762354-43762608	NONHSAT066592
3	lnc-PSG11-1	chr19:43544526-43544780	NONHSAT066579
4	lnc-PSG2-2	chr19:43576503-43576781	NONHSAT066580
5	lnc-CD177-1	chr19:43657431-43657763	ENSG00000227606.1
6	lnc-PSG6-1	chr19:43429925-43431729	NONHSAT066573
7	lnc-PSG2-4	chr19:43522922-43523199	NONHSAT066578
8	lnc-PSG4-2	chr19:43684499-43684748	NONHSAT066587
9	lnc-PSG2-1	chr19:43585939-43586423	NONHSAT066581
10	lnc-PSG2-5	chr19:43514422-43514579	NONHSAT066577
11	lnc-PSG6-1	chr19:43428286-43428976	NONHSAT066573
12	lnc-PSG9-2	chr19:43752643-43752798	NONHSAT066591
13	lnc-CD177-1	chr19:43658863-43659311	ENSG00000227606.1
14	lnc-PSG5-1	chr19:43696890-43697540	NONHSAT066588
15	lnc-PSG5-1	chr19:43698492-43699038	NONHSAT066588
16	lnc-PSG9-2	chr19:43724140-43724394	NONHSAT066591
17	lnc-PSG9-2	chr19:43724783-43725023	NONHSAT066593
18	lnc-PSG2-1	chr19:43586658-43586820	NONHSAT066581
19	lnc-PSG2-2	chr19:43575923-43576106	NONHSAT066580
20	lnc-PSG6-1	chr19:43429925-43430179	NR_073194
21	lnc-PSG9-2	chr19:43715943-43716627	NONHSAT066591
22	lnc-PSG9-2	chr19:43727043-43727110	NONHSAT066591
23	lnc-PSG11-1	chr19:43545168-43545400	NONHSAT066579
24	lnc-PSG2-5	chr19:43519268-43519426	NONHSAT066577
25	lnc-PSG9-2	chr19:43724140-43724394	NONHSAT066593
26	lnc-PSG4-3	chr19:43672274-43672355	NONHSAT066586
27	lnc-PSG2-3	chr19:43601248-43601512	NONHSAT066582
28	lnc-PSG9-2	chr19:43719405-43719531	NONHSAT066591
29	lnc-PSG2-5	chr19:43511982-43512194	NONHSAT066576
30	lnc-PSG2-3	chr19:43600608-43600855	NONHSAT066582
31	lnc-CD177-1	chr19:43657665-43657763	ENSG00000227606.1
32	lnc-PSG9-2	chr19:43734076-43734177	NONHSAT066591
33	lnc-PSG6-2	chr19:43454299-43454539	NONHSAT066575
34	lnc-PSG6-1	chr19:43439556-43439921	NR_073194
35	lnc-PSG4-1	chr19:43707241-43708403	NONHSAT066590
36	lnc-PSG6-1	chr19:43428284-43428976	NR_073194
37	lnc-PSG6-3	chr19:43372908-43374797	NONHSAT066572
38	lnc-PSG6-1	chr19:43430590-43430868	NR_073194
39	lnc-PSG9-2	chr19:43737376-43737446	NONHSAT066591
40	lnc-PSG9-2	chr19:43728324-43728464	NONHSAT066591
41	lnc-PSG11-1	chr19:43540021-43540112	NONHSAT066579
42	lnc-PSG6-2	chr19:43453655-43453909	NONHSAT066575
43	lnc-PSG6-1	chr19:43441165-43441330	NR_073194
44	lnc-PSG6-1	chr19:43441165-43441330	NONHSAT066574
45	lnc-PSG2-5	chr19:43514110-43514858	NONHSAT066576
46	lnc-CD177-1	chr19:43659324-43659477	ENSG00000227606.1
47	lnc-PSG4-3	chr19:43674207-43674717	NONHSAT066586
48	lnc-PSG4-1	chr19:43710321-43711451	NONHSAT066590
49	lnc-PSG6-1	chr19:43433594-43433872	NR_073194
50	lnc-PSG9-2	chr19:43763009-43764898	NONHSAT066592

No data

Variant related genes	Relation type
CEACAMP7	TF binding region
CEACAMP9	TF binding region
PSG5	TF binding region
PSG11	TF binding region
PSG6	TF binding region
CEACAMP10	TF binding region
PSG9	TF binding region
PSG4	TF binding region
CEACAMP8	TF binding region
PSG1	TF binding region
CEACAMP11	TF binding region
PSG2	TF binding region
ENSG00000227606	TF binding region
PSG7	TF binding region
CEACAMP7	CpG island
CEACAMP9	CpG island
PSG5	CpG island
PSG11	CpG island
PSG6	CpG island
CEACAMP10	CpG island
PSG9	CpG island
PSG4	CpG island
CEACAMP8	CpG island
PSG1	CpG island
CEACAMP11	CpG island
PSG2	CpG island
ENSG00000227606	CpG island
PSG7	CpG island
ENSG00000243137	chromatin interactions

Extended variants
information (count: 23522 )
Associated
traits (count: 88 )

Variant overlapped rSNPs/rCNVs (count:23522 , 50 per page) page: 1 2 3 4 5 6 7 ... 471

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1988065	chr19:43374601-43374602	Weak transcription Strong transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs113537262	chr19:43374618-43374619	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
3	rs150247538	chr19:43374619-43374620	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
4	rs192686295	chr19:43374669-43374670	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
5	rs556727526	chr19:43374675-43374676	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
6	rs577073786	chr19:43374692-43374693	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
7	rs185515999	chr19:43374701-43374702	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
8	rs553351714	chr19:43374722-43374723	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
9	rs573118815	chr19:43374723-43374724	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
10	rs542223809	chr19:43374729-43374730	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
11	rs562213699	chr19:43374738-43374739	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
12	rs190478383	chr19:43374745-43374746	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
13	rs1985620	chr19:43374753-43374754	Weak transcription Strong transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs374980285	chr19:43374759-43374760	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
15	rs572833508	chr19:43374809-43374810	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs546018812	chr19:43374812-43374813	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs546945086	chr19:43374815-43374816	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs567139510	chr19:43374824-43374825	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs367611560	chr19:43374862-43374863	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs371327915	chr19:43374868-43374869	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs138891002	chr19:43374869-43374870	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs547778311	chr19:43374872-43374873	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs564227954	chr19:43374890-43374891	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs567854510	chr19:43374896-43374897	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs61041467	chr19:43374905-43374906	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs185171739	chr19:43374915-43374916	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs570523883	chr19:43374931-43374932	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs188741498	chr19:43374952-43374953	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs149388128	chr19:43374958-43374959	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs573091580	chr19:43374961-43374962	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs10401873	chr19:43374968-43374969	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs376706949	chr19:43374976-43374977	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs181212768	chr19:43374986-43374987	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs185435999	chr19:43375008-43375009	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs544689843	chr19:43375009-43375010	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs370042952	chr19:43375024-43375025	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs189842123	chr19:43375031-43375032	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs578135955	chr19:43375038-43375039	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs543362817	chr19:43375053-43375054	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs375631940	chr19:43375055-43375056	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs182061085	chr19:43375070-43375071	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs375651546	chr19:43375128-43375129	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs187185149	chr19:43375160-43375161	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs547792297	chr19:43375220-43375221	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs561297062	chr19:43375233-43375234	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs561959323	chr19:43375239-43375240	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs530539918	chr19:43375240-43375241	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs529965510	chr19:43375241-43375242	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs111912306	chr19:43375242-43375243	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs550225241	chr19:43375244-43375245	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:88)

Disease	PMID	Source
Myelodysplastic syndrome	17634407	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	CNVD
Ovarian cancer	21720365	CNVD
Cancer	20164919	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Prostate cancer	18632612	CNVD
Autism	22495311	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Ductal carcinoma	22052326	CNVD
Congenital nephrotic syndrome	18421352	CNVD
Astrocytoma	17934521	CNVD
Leukemia	17361228	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Breast cancer	21858162	CNVD
Breast cancer	17603634	CNVD
Glioma	21971842	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Endometrial cancer	22040021	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Oligodendroglial tumors	17285580	CNVD
renal disease	20603712	CNVD
Salivary gland adenoid cystic carcinoma	17545515	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Breast cancer	21364760	CNVD
Invasive pancreatic ductal carcinoma	18765526	CNVD
Rhabdomyosarcoma	16790082	CNVD
Chordoma	18071362	CNVD
Urothelial carcinoma	21177765	CNVD
small cell lung cancer	20016488	CNVD
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Ovarian neoplasms	16753589	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Metanephric adenoma	20802469	CNVD
Acute myeloid leukemia	16864856	CNVD
Bladder cancer	21909424	CNVD
Medulloblastoma	16783165	CNVD
Gastric cancer	18160780	CNVD
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	19029149	CNVD
Breast cancer	20409316	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Multiple myeloma	16616336	CNVD
Renal cell carcinoma	18765545	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Astrocytoma	22246337	CNVD
Ovarian cancer	22174824	CNVD
Multiple myeloma	17550852	CNVD
Breast cancer	22522925	CNVD
Breast cancer	21509527	CNVD
Cancer	20164920	CNVD
Pancreatic cancer	17952125	CNVD
Ependymoma	20639864	CNVD
Autism	19492091	CNVD
Ovarian cancer	20800559	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16272173	CNVD
Spondylocostal dysostosis	21085971	CNVD
Nicotine metabolism	21956041	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Glioblastoma multiforme	17002787	CNVD
Ovarian cancer	20844748	CNVD
Breast cancer	17133270	CNVD
Colorectal cancer	20459617	CNVD
Lung adenocarcinoma	21935476	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Melanoma	20877625	CNVD
Ovarian cancer	21240255	CNVD
early-passage human iPS cells	21368824	CNVD
Primary Severe Spermatogenic Failure	20378930	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:1352 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:43357600-43378800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr19:43374000-43375400	Strong transcription	Placenta	Placenta
3	chr19:43374600-43378000	Weak transcription	NHDF-Ad	bronchial
4	chr19:43375400-43376800	Genic enhancers	Placenta	Placenta
5	chr19:43376200-43376800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
6	chr19:43376800-43377000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
7	chr19:43376800-43377000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
8	chr19:43376800-43378000	Strong transcription	Placenta	Placenta
9	chr19:43376800-43380200	Enhancers	HMEC	breast
10	chr19:43377000-43378400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
11	chr19:43377200-43378400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
12	chr19:43378000-43378200	Transcr. at gene 5' and 3'	Placenta	Placenta
13	chr19:43378000-43380600	Enhancers	NHDF-Ad	bronchial
14	chr19:43378200-43380000	Active TSS	Placenta	Placenta
15	chr19:43378200-43380000	Enhancers	NHEK	skin
16	chr19:43378400-43381600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
17	chr19:43378400-43381600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
18	chr19:43378400-43382200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
19	chr19:43378600-43378800	Enhancers	Muscle Satellite Cultured Cells	--
20	chr19:43378600-43379000	Enhancers	Breast Myoepithelial Primary Cells	Breast
21	chr19:43378600-43381600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
22	chr19:43378600-43382200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
23	chr19:43378800-43379200	Flanking Active TSS	Muscle Satellite Cultured Cells	--
24	chr19:43378800-43379600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
25	chr19:43378800-43380200	Enhancers	A549	lung
26	chr19:43378800-43380600	Enhancers	Hela-S3	cervix
27	chr19:43378800-43381000	Enhancers	NH-A	brain
28	chr19:43378800-43381400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
29	chr19:43378800-43381400	Enhancers	Osteobl	bone
30	chr19:43378800-43381600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
31	chr19:43378800-43381600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
32	chr19:43378800-43381600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
33	chr19:43378800-43381600	Enhancers	HSMM	muscle
34	chr19:43378800-43382200	Enhancers	NHLF	lung
35	chr19:43379000-43379200	Enhancers	Colon Smooth Muscle	Colon
36	chr19:43379000-43379200	Enhancers	Rectal Smooth Muscle	rectum
37	chr19:43379000-43380000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
38	chr19:43379200-43380200	Weak transcription	Rectal Smooth Muscle	rectum
39	chr19:43379200-43381600	Enhancers	Muscle Satellite Cultured Cells	--
40	chr19:43379200-43381600	Enhancers	HSMMtube	muscle
41	chr19:43379400-43380200	Weak transcription	Colon Smooth Muscle	Colon
42	chr19:43379400-43381400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
43	chr19:43379600-43380200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
44	chr19:43379800-43380400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
45	chr19:43380000-43380200	Flanking Active TSS	Placenta	Placenta
46	chr19:43380000-43380400	Flanking Active TSS	NHEK	skin
47	chr19:43380000-43382400	Enhancers	Breast Myoepithelial Primary Cells	Breast
48	chr19:43380200-43380400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
49	chr19:43380200-43380600	Enhancers	Placenta Amnion	Placenta Amnion
50	chr19:43380200-43380600	Flanking Active TSS	HMEC	breast

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