Variant report

Variant	esv2757811
Chromosome Location	chr2:78126389-78711032
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1403)
CpG islands
(count:306)
Chromatin interactive
region (count:39)
LncRNA
region (count:38)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1403 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:78389314-78389802	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:78653375-78653864	HepG2	liver:	n/a	n/a
3	ARID3A	chr2:78578391-78578636	HepG2	liver:	n/a	n/a
4	ARID3A	chr2:78578413-78578720	K562	blood:	n/a	n/a
5	ARID3A	chr2:78361077-78361118	K562	blood:	n/a	n/a
6	ARID3A	chr2:78532952-78532953	K562	blood:	n/a	n/a
7	ARID3A	chr2:78643666-78644757	HepG2	liver:	n/a	n/a
8	ARID3A	chr2:78336522-78336700	HepG2	liver:	n/a	n/a
9	ARID3A	chr2:78413821-78414186	HepG2	liver:	n/a	n/a
10	ARID3A	chr2:78487915-78488675	HepG2	liver:	n/a	n/a
11	ATF1	chr2:78408127-78408325	K562	blood:	n/a	n/a
12	ATF1	chr2:78215207-78215394	K562	blood:	n/a	n/a
13	ATF1	chr2:78166529-78166714	K562	blood:	n/a	n/a
14	ATF1	chr2:78361002-78361126	K562	blood:	n/a	n/a
15	BACH1	chr2:78477710-78477711	K562	blood:	n/a	n/a
16	BACH1	chr2:78368178-78368199	K562	blood:	n/a	n/a
17	BATF	chr2:78508306-78508624	GM12878	blood:	n/a	n/a
18	BATF	chr2:78428253-78428380	GM12878	blood:	n/a	n/a
19	BATF	chr2:78508305-78508535	GM12878	blood:	n/a	n/a
20	BCL11A	chr2:78508311-78508495	GM12878	blood:	n/a	n/a
21	BCL11A	chr2:78263040-78263247	H1-hESC	embryonic stem cell:	n/a	n/a
22	BDP1	chr2:78181978-78182355	K562	blood:	n/a	n/a
23	BHLHE40	chr2:78189217-78189406	HepG2	liver:	n/a	n/a
24	BHLHE40	chr2:78490807-78490864	GM12878	blood:	n/a	n/a
25	BHLHE40	chr2:78508455-78508636	GM12878	blood:	n/a	n/a
26	BHLHE40	chr2:78487986-78488343	HepG2	liver:	n/a	n/a
27	BHLHE40	chr2:78389461-78389669	HepG2	liver:	n/a	n/a
28	CBX3	chr2:78182081-78182419	K562	blood:	n/a	n/a
29	CBX3	chr2:78182148-78182464	K562	blood:	n/a	n/a
30	CBX3	chr2:78273156-78273427	K562	blood:	n/a	n/a
31	CBX3	chr2:78256529-78256863	K562	blood:	n/a	n/a
32	CBX3	chr2:78273160-78273446	K562	blood:	n/a	n/a
33	CBX3	chr2:78256534-78256829	K562	blood:	n/a	n/a
34	CCNT2	chr2:78252676-78252871	K562	blood:	n/a	n/a
35	CEBPB	chr2:78278617-78278979	IMR90	lung:	n/a	chr2:78278787-78278798
36	CEBPB	chr2:78167589-78167947	HepG2	liver:	n/a	chr2:78167759-78167770
37	CEBPB	chr2:78606574-78606774	A549	lung:	n/a	n/a
38	CEBPB	chr2:78413736-78414060	A549	lung:	n/a	chr2:78413883-78413892 chr2:78413883-78413892 chr2:78413883-78413892 chr2:78413881-78413894 chr2:78413882-78413893 chr2:78413881-78413894 chr2:78413881-78413892 chr2:78413883-78413892
39	CEBPB	chr2:78589457-78589745	A549	lung:	n/a	chr2:78589637-78589648
40	CEBPB	chr2:78257848-78257981	HepG2	liver:	n/a	chr2:78257886-78257897
41	CEBPB	chr2:78633266-78633466	HepG2	liver:	n/a	chr2:78633403-78633416 chr2:78633404-78633415
42	CEBPB	chr2:78336445-78336815	HepG2	liver:	n/a	n/a
43	CEBPB	chr2:78445211-78445551	A549	lung:	n/a	chr2:78445380-78445391
44	CEBPB	chr2:78376053-78376336	HepG2	liver:	n/a	chr2:78376191-78376202
45	CEBPB	chr2:78335197-78335393	HepG2	liver:	n/a	n/a
46	CEBPB	chr2:78152262-78152552	HepG2	liver:	n/a	chr2:78152391-78152402
47	CEBPB	chr2:78640615-78640922	K562	blood:	n/a	chr2:78640779-78640790 chr2:78640781-78640790
48	CEBPB	chr2:78445231-78445483	H1-hESC	embryonic stem cell:	n/a	chr2:78445380-78445391
49	CEBPB	chr2:78420652-78420781	K562	blood:	n/a	n/a
50	CEBPB	chr2:78213848-78214231	A549	lung:	n/a	chr2:78214166-78214177 chr2:78213968-78213979

(count:306 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:78182197-78182247	HCT-116	colon:	n/a
2	chr2:78182197-78182247	HCT-116	colon:	n/a
3	chr2:78182350-78182400	HEK293	kidney:	embryo
4	chr2:78182187-78182237	NH-A	brain:	n/a
5	chr2:78182187-78182237	GM19239	blood:	n/a
6	chr2:78182197-78182247	NHDF-neo	bronchial:	n/a
7	chr2:78263008-78263058	K562	blood:	n/a
8	chr2:78182350-78182400	ECC-1	luminal epithelium:	n/a
9	chr2:78182187-78182237	LNCaP	prostate:	n/a
10	chr2:78263008-78263058	HepG2	liver:	n/a
11	chr2:78263008-78263058	CMK	blood:	n/a
12	chr2:78182350-78182400	H1-hESC	embryonic stem cell:	embryo
13	chr2:78182187-78182237	AG04450	lung:	fetal
14	chr2:78182350-78182400	AG04449	skin:	fetal
15	chr2:78182350-78182400	T-47D	breast:	n/a
16	chr2:78545567-78545617	BE2_C	brain:	n/a
17	chr2:78182350-78182400	SKMC	muscle:	n/a
18	chr2:78182350-78182400	ovcar-3	ovarian:	n/a
19	chr2:78263008-78263058	SK-N-MC	brain:	n/a
20	chr2:78182350-78182400	AG09319	gingival:	n/a
21	chr2:78182350-78182400	AoSMC	blood vessel:	n/a
22	chr2:78263008-78263058	RPTEC	kidney:	n/a
23	chr2:78263008-78263058	GM12891	blood:	n/a
24	chr2:78182197-78182247	NH-A	brain:	n/a
25	chr2:78182197-78182247	GM12892	blood:	n/a
26	chr2:78263008-78263058	Hepatocyte	liver:	n/a
27	chr2:78182187-78182237	RPTEC	kidney:	n/a
28	chr2:78182350-78182400	HL-60	blood:	n/a
29	chr2:78182350-78182400	A549	lung:	n/a
30	chr2:78545567-78545617	GM06990	blood:	n/a
31	chr2:78182187-78182237	AG04449	skin:	fetal
32	chr2:78182350-78182400	NHDF-neo	bronchial:	n/a
33	chr2:78545567-78545617	ovcar-3	ovarian:	n/a
34	chr2:78182350-78182400	GM19239	blood:	n/a
35	chr2:78182197-78182247	Jurkat	blood:	n/a
36	chr2:78182197-78182247	HepG2	liver:	n/a
37	chr2:78182197-78182247	AG10803	skin:	n/a
38	chr2:78182197-78182247	GM06990	blood:	n/a
39	chr2:78182350-78182400	BJ	skin:	n/a
40	chr2:78182187-78182237	Hepatocyte	liver:	n/a
41	chr2:78182350-78182400	HepG2	liver:	n/a
42	chr2:78545567-78545617	HNPCEpiC	eye:	n/a
43	chr2:78545567-78545617	HPAEpiC	pulmonary alveolar:	n/a
44	chr2:78182187-78182237	GM12891	blood:	n/a
45	chr2:78545567-78545617	HEK293	kidney:	embryo
46	chr2:78263008-78263058	GM12878	blood:	n/a
47	chr2:78545567-78545617	HCF	heart:	n/a
48	chr2:78182350-78182400	HCF	heart:	n/a
49	chr2:78182350-78182400	GM12891	blood:	n/a
50	chr2:78263008-78263058	HRPEpiC	eye:	n/a

(count:39 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:78658362..78658925-chr2:79089675..79090181,2	MCF-7	breast:
2	chr2:78577011..78577791-chr8:96157456..96158424,2	MCF-7	breast:
3	chr2:78295743..78297764-chr2:78300068..78303067,2	K562	blood:
4	chr2:78658404..78659062-chr2:79206498..79207224,3	MCF-7	breast:
5	chr2:78637554..78639977-chr2:78766787..78768860,2	K562	blood:
6	chr2:78326493..78328202-chr2:78333273..78335963,2	K562	blood:
7	chr1:111007522..111008367-chr2:78191655..78192229,2	MCF-7	breast:
8	chr2:78687302..78689394-chr2:78702872..78704887,2	K562	blood:
9	chr2:78578299..78578916-chr2:79206809..79207351,2	MCF-7	breast:
10	chr2:78347733..78349406-chr2:78351881..78353903,2	K562	blood:
11	chr2:78326493..78328202-chr2:78333273..78335963,2	K562	blood:
12	chr2:78578903..78584135-chr2:78585848..78590226,6	K562	blood:
13	chr2:78295743..78297764-chr2:78300068..78303067,2	K562	blood:
14	chr17:59624355..59624932-chr2:78345304..78345966,2	MCF-7	breast:
15	chr2:78215424..78217099-chr2:78219299..78221415,2	K562	blood:
16	chr2:78695424..78698348-chr2:78698438..78701119,2	K562	blood:
17	chr2:78150104..78151070-chr7:109526792..109527641,2	MCF-7	breast:
18	chr2:78607954..78609567-chr2:78764622..78766807,2	K562	blood:
19	chr2:78695424..78698348-chr2:78698438..78701119,2	K562	blood:
20	chr2:78696080..78698215-chr2:78700355..78703022,2	K562	blood:
21	chr2:78519747..78522682-chr2:78785137..78786876,2	K562	blood:
22	chr2:78696080..78698215-chr2:78700355..78703022,2	K562	blood:
23	chr2:78538765..78541253-chr2:78550718..78553114,2	K562	blood:
24	chr2:78577613..78578539-chr2:79206466..79207847,3	MCF-7	breast:
25	chr2:78578903..78584135-chr2:78585848..78590226,6	K562	blood:
26	chr2:78578454..78579130-chr2:79226516..79227199,2	MCF-7	breast:
27	chr2:78552005..78554249-chr2:78556086..78558009,2	K562	blood:
28	chr2:78300847..78302731-chr2:78308537..78310502,2	K562	blood:
29	chr2:78687302..78689394-chr2:78702872..78704887,2	K562	blood:
30	chr2:78694367..78697060-chr2:78697829..78699693,2	MCF-7	breast:
31	chr2:78538765..78541253-chr2:78550718..78553114,2	K562	blood:
32	chr2:78347906..78350697-chr2:78350756..78353381,2	K562	blood:
33	chr2:78347906..78350697-chr2:78350756..78353381,2	K562	blood:
34	chr2:78347733..78349406-chr2:78351881..78353903,2	K562	blood:
35	chr2:78300847..78302731-chr2:78308537..78310502,2	K562	blood:
36	chr2:78552005..78554249-chr2:78556086..78558009,2	K562	blood:
37	chr2:78215424..78217099-chr2:78219299..78221415,2	K562	blood:
38	chr2:78694367..78697060-chr2:78697829..78699693,2	MCF-7	breast:
39	chr2:78709311..78711382-chr2:78715661..78717389,2	K562	blood:

(count:38 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-REG3G-4	chr2:78144363-78144530	NR_110286
2	lnc-REG3G-4	chr2:78144829-78145134	NR_110286
3	lnc-REG3G-4	chr2:78144829-78145135	XLOC_001542
4	lnc-REG3G-8	chr2:78174151-78174300	NONHSAT071839
5	lnc-LRRTM4-3	chr2:78517514-78517857	NR_110288
6	lnc-LRRTM4-3	chr2:78229100-78229271	NONHSAT071835
7	lnc-LRRTM4-3	chr2:78683574-78683857	NONHSAT071835
8	lnc-LRRTM4-8	chr2:78371022-78371323	ucscGeneNc_uc002snu_2
9	lnc-REG3G-4	chr2:78143060-78143219	XLOC_001542
10	lnc-REG3G-4	chr2:78144828-78145135	NONHSAT071836
11	lnc-LRRTM4-3	chr2:78639919-78640220	NONHSAT071847
12	lnc-REG3G-4	chr2:78144363-78144530	XLOC_001542
13	lnc-LRRTM4-3	chr2:78639673-78640302	NONHSAT071846
14	lnc-REG3G-8	chr2:78208133-78208440	NONHSAT071839
15	lnc-REG3G-4	chr2:78143032-78143219	NONHSAT071836
16	lnc-REG3G-3	chr2:78321763-78321902	XLOC_001543
17	lnc-LRRTM4-2	chr2:78176532-78176551	XLOC_002173
18	lnc-LRRTM4-3	chr2:78214578-78215904	NONHSAT071835
19	lnc-REG3G-8	chr2:78192534-78192764	NONHSAT071839
20	lnc-REG3G-3	chr2:78322790-78322968	XLOC_001543
21	lnc-REG1B-7	chr2:78678545-78678570	NONHSAT071849
22	lnc-REG3G-4	chr2:78143060-78143219	NR_110286
23	lnc-REG3G-8	chr2:78175271-78175410	NONHSAT071839
24	lnc-REG3G-7	chr2:78664976-78666047	NONHSAT071848
25	lnc-REG3G-4	chr2:78144362-78144530	NONHSAT071836
26	lnc-LRRTM4-3	chr2:78225204-78225307	NONHSAT071835
27	lnc-LRRTM4-3	chr2:78252450-78252550	NONHSAT071835
28	lnc-REG3G-4	chr2:78144363-78144530	XLOC_001542
29	lnc-REG3G-3	chr2:78339185-78339226	XLOC_001543
30	lnc-REG3G-3	chr2:78354625-78354877	XLOC_001543
31	lnc-REG3G-3	chr2:78320703-78320792	XLOC_001543
32	lnc-REG3G-4	chr2:78143033-78143219	XLOC_001542
33	lnc-REG3G-8	chr2:78169364-78169425	NONHSAT071839
34	lnc-REG3G-4	chr2:78144874-78145117	XLOC_001542
35	lnc-REG1B-7	chr2:78679696-78680040	NONHSAT071849
36	lnc-LRRTM4-3	chr2:78637204-78640302	NONHSAT071835
37	lnc-REG3G-8	chr2:78187674-78187885	NONHSAT071839
38	lnc-LRRTM4-2	chr2:78178164-78178621	XLOC_002173

No data

Variant related genes	Relation type
ENSG00000233605	TF binding region
CYCSP6	TF binding region
ENSG00000229494	TF binding region
ENSG00000270470	TF binding region
ENSG00000233605	CpG island
CYCSP6	CpG island
ENSG00000229494	CpG island
ENSG00000270470	CpG island
PDCD4	miRNA target sites
CELF2	miRNA target sites

Extended variants
information (count: 11377 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:11377 , 50 per page) page: 1 2 3 4 5 6 7 ... 228

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs569745026	chr2:78126455-78126456	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs538349614	chr2:78126457-78126458	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs554183024	chr2:78126466-78126467	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs13019185	chr2:78126573-78126574	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs574974324	chr2:78126587-78126588	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs114486145	chr2:78126591-78126592	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs149639965	chr2:78126625-78126626	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs574355635	chr2:78126633-78126634	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs144353010	chr2:78126634-78126635	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs112079607	chr2:78126679-78126680	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs532686463	chr2:78126733-78126734	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs77809277	chr2:78126760-78126761	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs13399169	chr2:78126791-78126792	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs185663848	chr2:78126817-78126818	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs548774065	chr2:78126869-78126870	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs10192753	chr2:78126898-78126899	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs531193002	chr2:78126899-78126900	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs549791690	chr2:78126906-78126907	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs536824405	chr2:78126920-78126921	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs569538185	chr2:78126980-78126981	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs561658645	chr2:78127001-78127002	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs189214885	chr2:78127081-78127082	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs180887506	chr2:78127112-78127113	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs183474828	chr2:78127157-78127158	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs565407633	chr2:78127178-78127179	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs80076181	chr2:78127184-78127185	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs75202288	chr2:78127185-78127186	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs112183788	chr2:78127209-78127210	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs77841496	chr2:78127210-78127211	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs79471882	chr2:78127212-78127213	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs369592541	chr2:78127214-78127215	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs57460336	chr2:78127215-78127216	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs62163504	chr2:78127216-78127217	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs376136225	chr2:78127218-78127219	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs70956657	chr2:78127222-78127223	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs546203404	chr2:78127226-78127227	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs574395391	chr2:78127270-78127271	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs116240684	chr2:78127274-78127275	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs112741284	chr2:78127285-78127286	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs188551378	chr2:78127287-78127288	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs564569802	chr2:78127411-78127412	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs577154091	chr2:78127421-78127422	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs546308093	chr2:78127501-78127502	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs181345199	chr2:78127502-78127503	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs144789035	chr2:78127511-78127512	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs542454528	chr2:78127566-78127567	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs562220061	chr2:78127602-78127603	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs531273071	chr2:78127657-78127658	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs118055722	chr2:78127663-78127664	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs563322537	chr2:78127710-78127711	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:61)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17387387	CNVD
Neuroblastoma	17533364	CNVD
Neuroblastoma	18923191	CNVD
Endometrial cancer	22040021	CNVD
Adrenal tumor	17535989	CNVD
Breast cancer	21264507	CNVD
Basal cell lymphoma	17053054	CNVD
Medulloblastoma	17522785	CNVD
Cancer	23418310	CNVD
Medulloblastoma	21979893	CNVD
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Follicular lymphoma	20505157	CNVD
Autism	17483303	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Medulloblastoma	20607354	CNVD
Autism	22495311	CNVD
Autism	18522746	CNVD
Neurodevelopmental disorder	22521361	CNVD
Lung cancer	18438408	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Seminomas	18059402	CNVD
Testicular germ cell tumor	18059402	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Renal cell carcinoma	18765545	CNVD
Myxofibrosarcoma	16751306	CNVD
small cell lung cancer	20016488	CNVD
Acute myeloid leukemia	21251322	CNVD
Mental retardation	17124404	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Cancer	17440070	CNVD
Myelofibrosis	22110671	CNVD
Attention deficit hyperactivity disorder	21324949	CNVD
Breast cancer	16272173	CNVD
Epilepsy	22083797	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:460 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:78125200-78127200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
2	chr2:78127200-78128200	Enhancers	iPS-15b Cell Line	embryonic stem cell
3	chr2:78127400-78127800	Enhancers	Breast Myoepithelial Primary Cells	Breast
4	chr2:78127600-78128200	Enhancers	ES-I3 Cell Line	embryonic stem cell
5	chr2:78129400-78133200	Weak transcription	Pancreas	Pancrea
6	chr2:78151800-78152000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr2:78152600-78152800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr2:78157000-78157400	Enhancers	iPS-15b Cell Line	embryonic stem cell
9	chr2:78159000-78159400	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr2:78159400-78160400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr2:78160400-78161200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr2:78192800-78193200	Active TSS	ES-I3 Cell Line	embryonic stem cell
13	chr2:78193200-78195000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
14	chr2:78194800-78195200	Active TSS	HUES6 Cell Line	embryonic stem cell
15	chr2:78194800-78195200	Active TSS	iPS-20b Cell Line	embryonic stem cell
16	chr2:78195000-78195200	Active TSS	ES-I3 Cell Line	embryonic stem cell
17	chr2:78195200-78195600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
18	chr2:78195200-78200200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
19	chr2:78195600-78195800	Active TSS	ES-I3 Cell Line	embryonic stem cell
20	chr2:78195800-78199600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
21	chr2:78199200-78201800	Enhancers	HUES48 Cell Line	embryonic stem cell
22	chr2:78199600-78200200	Enhancers	ES-I3 Cell Line	embryonic stem cell
23	chr2:78199800-78200000	Enhancers	iPS-18 Cell Line	embryonic stem cell
24	chr2:78200000-78200400	Enhancers	HUES6 Cell Line	embryonic stem cell
25	chr2:78200000-78200800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
26	chr2:78200200-78200400	Enhancers	iPS-20b Cell Line	embryonic stem cell
27	chr2:78200200-78201200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
28	chr2:78200400-78200600	Weak transcription	HUES6 Cell Line	embryonic stem cell
29	chr2:78200400-78201400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
30	chr2:78200600-78201000	Enhancers	HUES6 Cell Line	embryonic stem cell
31	chr2:78200600-78201800	Enhancers	iPS-15b Cell Line	embryonic stem cell
32	chr2:78200800-78201200	Enhancers	iPS-18 Cell Line	embryonic stem cell
33	chr2:78200800-78201600	Enhancers	HUES64 Cell Line	embryonic stem cell
34	chr2:78201200-78201400	Enhancers	ES-I3 Cell Line	embryonic stem cell
35	chr2:78201200-78201400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
36	chr2:78201400-78201800	Enhancers	iPS-18 Cell Line	embryonic stem cell
37	chr2:78201400-78202000	Enhancers	iPS-20b Cell Line	embryonic stem cell
38	chr2:78201400-78204200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
39	chr2:78204600-78205000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
40	chr2:78220200-78220800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
41	chr2:78226200-78226800	Enhancers	Muscle Satellite Cultured Cells	--
42	chr2:78226200-78227000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
43	chr2:78226600-78227400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
44	chr2:78226800-78227200	Weak transcription	Muscle Satellite Cultured Cells	--
45	chr2:78227200-78227400	Enhancers	Muscle Satellite Cultured Cells	--
46	chr2:78227400-78229200	Weak transcription	Muscle Satellite Cultured Cells	--
47	chr2:78229200-78229400	Enhancers	Muscle Satellite Cultured Cells	--
48	chr2:78229400-78229800	Weak transcription	Muscle Satellite Cultured Cells	--
49	chr2:78229800-78230200	Enhancers	Muscle Satellite Cultured Cells	--
50	chr2:78237000-78237200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin

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