Variant report

Variant	esv3429093
Chromosome Location	chr14:36674701-36827119
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1629)
CpG islands
(count:1160)
Chromatin interactive
region (count:88)
LncRNA
region (count:21)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1629 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:36725743-36725753	K562	blood:	n/a	n/a
2	ARID3A	chr14:36710498-36710696	K562	blood:	n/a	n/a
3	ARID3A	chr14:36769601-36770046	HepG2	liver:	n/a	n/a
4	ARID3A	chr14:36733302-36734246	K562	blood:	n/a	n/a
5	ARID3A	chr14:36784635-36784815	K562	blood:	n/a	n/a
6	ARID3A	chr14:36740785-36740980	K562	blood:	n/a	n/a
7	ARID3A	chr14:36786874-36787050	HepG2	liver:	n/a	n/a
8	ARID3A	chr14:36789827-36789998	K562	blood:	n/a	n/a
9	ARID3A	chr14:36789353-36790203	HepG2	liver:	n/a	n/a
10	ARID3A	chr14:36730001-36730419	K562	blood:	n/a	n/a
11	ARID3A	chr14:36723506-36723776	HepG2	liver:	n/a	n/a
12	ARID3A	chr14:36677815-36678352	HepG2	liver:	n/a	n/a
13	ARID3A	chr14:36754518-36754696	K562	blood:	n/a	n/a
14	ARID3A	chr14:36754429-36754629	HepG2	liver:	n/a	n/a
15	ARID3A	chr14:36785526-36785702	K562	blood:	n/a	n/a
16	ARID3A	chr14:36787931-36788470	HepG2	liver:	n/a	n/a
17	ATF1	chr14:36789684-36790159	K562	blood:	n/a	n/a
18	ATF1	chr14:36733817-36734157	K562	blood:	n/a	n/a
19	ATF1	chr14:36707940-36708121	K562	blood:	n/a	n/a
20	ATF2	chr14:36789725-36790108	GM12878	blood:	n/a	n/a
21	ATF2	chr14:36769598-36769998	GM12878	blood:	n/a	n/a
22	ATF2	chr14:36789693-36790117	H1-hESC	embryonic stem cell:	n/a	n/a
23	ATF2	chr14:36789612-36790132	GM12878	blood:	n/a	n/a
24	ATF2	chr14:36769592-36769971	GM12878	blood:	n/a	n/a
25	ATF3	chr14:36789354-36790107	HepG2	liver:	n/a	chr14:36789882-36789890 chr14:36789880-36789890 chr14:36789879-36789892 chr14:36789880-36789893 chr14:36789846-36789855 chr14:36789871-36789891
26	ATF3	chr14:36789765-36789985	GM12878	blood:	n/a	chr14:36789882-36789890 chr14:36789880-36789890 chr14:36789879-36789892 chr14:36789880-36789893 chr14:36789846-36789855 chr14:36789871-36789891
27	ATF3	chr14:36789635-36790064	H1-hESC	embryonic stem cell:	n/a	chr14:36789882-36789890 chr14:36789880-36789890 chr14:36789879-36789892 chr14:36789880-36789893 chr14:36789846-36789855 chr14:36789871-36789891
28	ATF3	chr14:36789736-36790012	K562	blood:	n/a	chr14:36789882-36789890 chr14:36789880-36789890 chr14:36789879-36789892 chr14:36789880-36789893 chr14:36789846-36789855 chr14:36789871-36789891
29	BACH1	chr14:36723518-36723757	H1-hESC	embryonic stem cell:	n/a	n/a
30	BACH1	chr14:36764628-36764681	H1-hESC	embryonic stem cell:	n/a	n/a
31	BATF	chr14:36784726-36785054	GM12878	blood:	n/a	chr14:36784842-36784853
32	BATF	chr14:36769541-36769888	GM12878	blood:	n/a	chr14:36769803-36769813
33	BATF	chr14:36784705-36785059	GM12878	blood:	n/a	chr14:36784842-36784853
34	BCL11A	chr14:36769496-36769723	GM12878	blood:	n/a	n/a
35	BCL3	chr14:36784682-36784987	GM12878	blood:	n/a	chr14:36784811-36784820
36	BCL3	chr14:36789549-36790347	A549	lung:	n/a	n/a
37	BHLHE40	chr14:36692826-36693409	K562	blood:	n/a	n/a
38	BHLHE40	chr14:36733661-36734189	K562	blood:	n/a	n/a
39	BHLHE40	chr14:36784748-36785137	GM12878	blood:	n/a	n/a
40	BHLHE40	chr14:36707944-36708015	K562	blood:	n/a	n/a
41	BHLHE40	chr14:36789595-36790169	K562	blood:	n/a	n/a
42	BHLHE40	chr14:36754810-36755151	K562	blood:	n/a	n/a
43	BRCA1	chr14:36789668-36790245	HepG2	liver:	n/a	n/a
44	BRCA1	chr14:36789033-36790188	Hela-S3	cervix:	n/a	n/a
45	BRCA1	chr14:36788746-36788783	Hela-S3	cervix:	n/a	n/a
46	CBX3	chr14:36733668-36734157	K562	blood:	n/a	n/a
47	CBX3	chr14:36826062-36826365	K562	blood:	n/a	n/a
48	CBX3	chr14:36789680-36790403	K562	blood:	n/a	n/a
49	CBX3	chr14:36826125-36826377	K562	blood:	n/a	n/a
50	CBX3	chr14:36750501-36750838	K562	blood:	n/a	n/a

(count:1160 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:36789810-36789860	HRE	kidney:	n/a
2	chr14:36789810-36789860	HRE	kidney:	n/a
3	chr14:36711182-36711232	HNPCEpiC	eye:	n/a
4	chr14:36789886-36789936	HL-60	blood:	n/a
5	chr14:36789810-36789860	AoSMC	blood vessel:	n/a
6	chr14:36741794-36741844	GM06990	blood:	n/a
7	chr14:36765887-36765937	HRPEpiC	eye:	n/a
8	chr14:36743725-36743775	HRPEpiC	eye:	n/a
9	chr14:36737696-36737746	AG04449	skin:	fetal
10	chr14:36737696-36737746	AoSMC	blood vessel:	n/a
11	chr14:36684553-36684603	HCPEpiC	choroid plexus:	n/a
12	chr14:36743725-36743775	HCF	heart:	n/a
13	chr14:36691116-36691166	HEEpiC	esophagus:	n/a
14	chr14:36698832-36698882	HIPEpiC	eye:	n/a
15	chr14:36708508-36708558	BJ	skin:	n/a
16	chr14:36737696-36737746	HL-60	blood:	n/a
17	chr14:36711182-36711232	GM12891	blood:	n/a
18	chr14:36789985-36790035	PrEC	prostate:	n/a
19	chr14:36708508-36708558	SK-N-SH_RA	brain:	n/a
20	chr14:36789810-36789860	AG04450	lung:	fetal
21	chr14:36691116-36691166	GM19239	blood:	n/a
22	chr14:36743725-36743775	SK-N-SH_RA	brain:	n/a
23	chr14:36789691-36789741	AG09319	gingival:	n/a
24	chr14:36789985-36790035	SK-N-MC	brain:	n/a
25	chr14:36789810-36789860	ProgFib	skin:	n/a
26	chr14:36737696-36737746	PFSK-1	brain:	n/a
27	chr14:36695421-36695471	HAEpiC	amniotic membrane:	n/a
28	chr14:36708508-36708558	PrEC	prostate:	n/a
29	chr14:36789810-36789860	SAEC	small airway:	n/a
30	chr14:36708508-36708558	HRE	kidney:	n/a
31	chr14:36695421-36695471	AG04450	lung:	fetal
32	chr14:36789810-36789860	SK-N-SH_RA	brain:	n/a
33	chr14:36691116-36691166	AoSMC	blood vessel:	n/a
34	chr14:36691116-36691166	SKMC	muscle:	n/a
35	chr14:36684553-36684603	SK-N-MC	brain:	n/a
36	chr14:36743725-36743775	LNCaP	prostate:	n/a
37	chr14:36708508-36708558	NT2-D1	testis:	n/a
38	chr14:36789886-36789936	GM06990	blood:	n/a
39	chr14:36790242-36790292	HL-60	blood:	n/a
40	chr14:36691116-36691166	ProgFib	skin:	n/a
41	chr14:36698832-36698882	HRPEpiC	eye:	n/a
42	chr14:36741645-36741695	ECC-1	luminal epithelium:	n/a
43	chr14:36789886-36789936	HEEpiC	esophagus:	n/a
44	chr14:36708508-36708558	HCT-116	colon:	n/a
45	chr14:36741794-36741844	SK-N-SH	brain:	n/a
46	chr14:36741645-36741695	SK-N-MC	brain:	n/a
47	chr14:36790242-36790292	BJ	skin:	n/a
48	chr14:36789488-36789538	PrEC	prostate:	n/a
49	chr14:36789810-36789860	MCF10A-Er-Src	breast:	n/a
50	chr14:36790242-36790292	Hepatocyte	liver:	n/a

(count:88 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr14:36676641..36677323-chr14:36994485..36995249,2	MCF-7	breast:
2	chr14:36750490..36753269-chr14:36756385..36758922,2	K562	blood:
3	chr14:36723640..36727122-chr14:36730351..36734194,3	MCF-7	breast:
4	chr14:36692567..36694676-chr14:36694678..36697500,2	MCF-7	breast:
5	chr14:36744274..36747863-chr14:36750773..36754664,4	K562	blood:
6	chr14:36747753..36750130-chr14:36837234..36840040,2	K562	blood:
7	chr14:36747888..36750635-chr14:36759343..36761098,2	K562	blood:
8	chr14:36768912..36770474-chr14:36787292..36789766,2	MCF-7	breast:
9	chr14:36539400..36540077-chr14:36676431..36676939,2	MCF-7	breast:
10	chr14:36674915..36676965-chr14:36682336..36684243,2	K562	blood:
11	chr14:36774640..36776851-chr14:36779144..36781211,2	K562	blood:
12	chr14:36744330..36746505-chr14:36753051..36754941,2	MCF-7	breast:
13	chr14:36683929..36686660-chr14:36694552..36697045,2	MCF-7	breast:
14	chr1:53308102..53308983-chr14:36776394..36777212,2	MCF-7	breast:
15	chr14:36676984..36677491-chr14:36843145..36844040,2	MCF-7	breast:
16	chr14:36676468..36677430-chr14:36842915..36843825,2	MCF-7	breast:
17	chr14:36739666..36742566-chr14:36744671..36747415,2	K562	blood:
18	chr14:36779773..36781769-chr14:36782151..36784795,2	K562	blood:
19	chr14:36789374..36789875-chr8:119123638..119124514,2	Hela-S3	cervix:
20	chr14:36779773..36781769-chr14:36782151..36784795,2	K562	blood:
21	chr14:36759414..36761344-chr14:36764422..36766950,2	MCF-7	breast:
22	chr14:36733094..36734657-chr14:36742759..36745467,2	K562	blood:
23	chr14:36778847..36780826-chr14:36784208..36786054,2	MCF-7	breast:
24	chr14:36777645..36780229-chr14:36786756..36790572,4	MCF-7	breast:
25	chr14:36682051..36684620-chr14:36711169..36712893,2	K562	blood:
26	chr14:36793727..36795435-chr14:36796192..36797833,2	MCF-7	breast:
27	chr14:36778592..36784393-chr14:36785409..36790832,9	K562	blood:
28	chr14:36733892..36735443-chr14:36737409..36739659,2	K562	blood:
29	chr14:36574817..36577069-chr14:36759896..36761522,2	K562	blood:
30	chr14:36780477..36782487-chr14:36786743..36788959,2	MCF-7	breast:
31	chr14:36538483..36541249-chr14:36788541..36791272,2	MCF-7	breast:
32	chr10:69141438..69142223-chr14:36735859..36736731,2	MCF-7	breast:
33	chr14:36772767..36774449-chr14:36777469..36780447,2	K562	blood:
34	chr14:36793727..36795435-chr14:36796192..36797833,2	MCF-7	breast:
35	chr14:36780690..36783423-chr14:36785409..36787697,2	K562	blood:
36	chr14:36788593..36791761-chr14:36792192..36795536,3	K562	blood:
37	chr14:36764356..36766660-chr14:36769237..36771689,3	K562	blood:
38	chr14:36738662..36740717-chr14:36743320..36745881,2	MCF-7	breast:
39	chr14:36752607..36756130-chr14:36756602..36759411,3	K562	blood:
40	chr14:36733094..36734657-chr14:36742759..36745467,2	K562	blood:
41	chr14:36752607..36756130-chr14:36756602..36759411,3	K562	blood:
42	chr14:36763341..36766160-chr14:36772206..36774961,2	K562	blood:
43	chr14:36733892..36736595-chr14:36737409..36740158,4	K562	blood:
44	chr14:36781444..36784031-chr14:36790836..36792756,2	K562	blood:
45	chr14:36726358..36728728-chr14:36730369..36733275,2	MCF-7	breast:
46	chr14:36783190..36784933-chr14:36788355..36791806,3	MCF-7	breast:
47	chr14:36733892..36735443-chr14:36737409..36739659,2	K562	blood:
48	chr14:36784989..36787450-chr14:36787865..36790918,4	K562	blood:
49	chr14:36676675..36678036-chr14:36919496..36920913,3	MCF-7	breast:
50	chr14:36783190..36784933-chr14:36788355..36791806,3	MCF-7	breast:

(count:21 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-BRMS1L-3	chr14:36683885-36684264	XLOC_010797
2	lnc-BRMS1L-4	chr14:36747208-36747276	XLOC_010799
3	lnc-BRMS1L-3	chr14:36691503-36691569	XLOC_010798
4	lnc-BRMS1L-2	chr14:36684580-36684697	NONHSAT036417
5	lnc-BRMS1L-3	chr14:36690500-36690689	XLOC_010798
6	lnc-PAX9-10	chr14:36785664-36785887	uc_374_+
7	lnc-BRMS1L-4	chr14:36758889-36759236	XLOC_010799
8	lnc-BRMS1L-3	chr14:36704526-36704816	XLOC_010798
9	lnc-BRMS1L-3	chr14:36684580-36685567	XLOC_010797
10	lnc-BRMS1L-4	chr14:36741574-36742599	XLOC_010799
11	lnc-BRMS1L-3	chr14:36704530-36704814	ENSG00000258844
12	lnc-MBIP-1	chr14:36741625-36742658	XLOC_010997
13	lnc-BRMS1L-3	chr14:36684580-36684721	ENSG00000258844
14	lnc-BRMS1L-3	chr14:36683813-36684264	ENSG00000258844
15	lnc-SFTA3-2	chr14:36785664-36785887	uc_374_-
16	lnc-MBIP-1	chr14:36738278-36738517	XLOC_010997
17	lnc-BRMS1L-2	chr14:36691502-36691569	NONHSAT036421
18	lnc-BRMS1L-3	chr14:36690500-36690685	XLOC_010798
19	lnc-BRMS1L-2	chr14:36684165-36684264	NONHSAT036417
20	lnc-MBIP-4	chr14:36700761-36700980	NONHSAT036424
21	lnc-BRMS1L-2	chr14:36690499-36690689	NONHSAT036421

No data

Variant related genes	Relation type
RN7SKP21	TF binding region
MBIP	TF binding region
ENSG00000258844	TF binding region
RN7SKP21	CpG island
MBIP	CpG island
ENSG00000258844	CpG island
ENSG00000203995	chromatin interactions
ENSG00000257585	chromatin interactions
ENSG00000182197	chromatin interactions
ENSG00000151332	chromatin interactions
ENSG00000258844	chromatin interactions
AKT3	miRNA target sites
SNAI2	miRNA target sites
SHPK	miRNA target sites
TNFRSF11B	miRNA target sites

Extended variants
information (count: 4355 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:4355 , 50 per page) page: 1 2 3 4 5 6 7 ... 88

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs146970351	chr14:36674946-36674947	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs149770623	chr14:36674966-36674967	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs144860746	chr14:36675015-36675016	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs10139973	chr14:36675034-36675035	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs535853712	chr14:36675057-36675058	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs558026358	chr14:36675068-36675069	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs555711490	chr14:36675093-36675094	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs148581538	chr14:36675111-36675112	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs538759119	chr14:36675119-36675120	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs144430514	chr14:36675148-36675149	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs572644037	chr14:36675163-36675164	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs541217818	chr14:36675168-36675169	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs187015603	chr14:36675203-36675204	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs575149628	chr14:36675242-36675243	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs543863218	chr14:36675245-36675246	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs4638466	chr14:36675247-36675248	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs577155877	chr14:36675252-36675253	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs546320431	chr14:36675310-36675311	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs559591293	chr14:36675367-36675368	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs191401141	chr14:36675391-36675392	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs4553500	chr14:36675397-36675398	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs183370052	chr14:36675422-36675423	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs185578733	chr14:36675423-36675424	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs549648888	chr14:36675437-36675438	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs544583247	chr14:36675498-36675499	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs189950713	chr14:36675546-36675547	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs116380399	chr14:36675552-36675553	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs567843626	chr14:36675621-36675622	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs565595268	chr14:36675638-36675639	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs535244707	chr14:36675655-36675656	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs146598458	chr14:36675741-36675742	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs575066685	chr14:36675743-36675744	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs537777045	chr14:36675817-36675818	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs140296847	chr14:36675835-36675836	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs76615311	chr14:36675837-36675838	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs1952707	chr14:36675857-36675858	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs117682617	chr14:36675895-36675896	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs182277831	chr14:36675933-36675934	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs541898224	chr14:36675935-36675936	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs560783072	chr14:36675938-36675939	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs150860357	chr14:36676078-36676079	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs551844315	chr14:36676079-36676080	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs549710303	chr14:36676094-36676095	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs563387251	chr14:36676224-36676225	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs530246150	chr14:36676239-36676240	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs144020628	chr14:36676342-36676343	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs560137106	chr14:36676365-36676366	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs565786499	chr14:36676374-36676375	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs188047490	chr14:36676453-36676454	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs548293778	chr14:36676461-36676462	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:66)

Disease	PMID	Source
Esophageal cancer	21851588	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
High-proliferative meningiomas	17937814	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Non-small cell lung cancer	21044232	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Medulloblastoma	21979893	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Hepatocellular carcinoma	22174799	CNVD
Colorectal cancer	16774939	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	17899364	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Chronic myeloid leukemia	20724749	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Wilms tumour	21544195	CNVD
Esophageal cancer	20955586	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Burkitt''s lymphoma	19759907	CNVD
Lung cancer	18438408	CNVD
Urothelial carcinoma	21177765	CNVD
Multiple myeloma	17550852	CNVD
Breast cancer	21785460	CNVD
Cancer	21129771	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Lung cancer	17925434	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	21569311	CNVD
Lung cancer	21911935	CNVD
Myelofibrosis	22110671	CNVD
abnormal development	18461090	CNVD
Prostate cancer	21298110	CNVD
Metanephric adenoma	20802469	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	21858162	CNVD
Lung cancer	20031968	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Osteosarcoma	21215367	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD

Chromatin state (count:2033 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:36677200-36677600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr14:36677600-36681400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr14:36678000-36678400	Enhancers	Brain Inferior Temporal Lobe	brain
4	chr14:36681400-36684200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr14:36682800-36683200	Enhancers	Gastric	stomach
6	chr14:36682800-36683400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr14:36682800-36683400	Enhancers	iPS-20b Cell Line	embryonic stem cell
8	chr14:36682800-36683400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
9	chr14:36682800-36683400	Enhancers	Brain Cingulate Gyrus	brain
10	chr14:36682800-36684400	Enhancers	HUES6 Cell Line	embryonic stem cell
11	chr14:36682800-36684400	Enhancers	iPS-18 Cell Line	embryonic stem cell
12	chr14:36682800-36684800	Enhancers	iPS-15b Cell Line	embryonic stem cell
13	chr14:36682800-36685200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
14	chr14:36682800-36685200	Enhancers	HUES64 Cell Line	embryonic stem cell
15	chr14:36683000-36683200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
16	chr14:36683000-36683600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
17	chr14:36683000-36684000	Enhancers	ES-I3 Cell Line	embryonic stem cell
18	chr14:36683000-36684200	Enhancers	HMEC	breast
19	chr14:36683000-36685000	Enhancers	HUES48 Cell Line	embryonic stem cell
20	chr14:36683200-36685400	Weak transcription	Gastric	stomach
21	chr14:36683400-36683800	Enhancers	H1 Cell Line	embryonic stem cell
22	chr14:36683400-36683800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr14:36683400-36684400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr14:36683400-36690200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
25	chr14:36683600-36684000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr14:36683800-36684000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
27	chr14:36683800-36684400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr14:36684000-36684400	Enhancers	H1 Cell Line	embryonic stem cell
29	chr14:36684000-36684600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
30	chr14:36684000-36684800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
31	chr14:36684000-36692200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
32	chr14:36684200-36685000	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr14:36684200-36686400	Weak transcription	HMEC	breast
34	chr14:36684400-36686600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr14:36684400-36692200	Weak transcription	HUES6 Cell Line	embryonic stem cell
36	chr14:36684600-36685000	Bivalent Enhancer	Stomach Mucosa	stomach
37	chr14:36684800-36690200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
38	chr14:36685000-36686600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr14:36685000-36690200	Weak transcription	HUES48 Cell Line	embryonic stem cell
40	chr14:36685200-36686600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
41	chr14:36685200-36690400	Weak transcription	HUES64 Cell Line	embryonic stem cell
42	chr14:36685400-36685600	Enhancers	Gastric	stomach
43	chr14:36685400-36686400	Active TSS	Lung	lung
44	chr14:36686000-36686400	Enhancers	Rectal Mucosa Donor 31	rectum
45	chr14:36686000-36686600	Bivalent Enhancer	Stomach Mucosa	stomach
46	chr14:36686400-36686600	Bivalent Enhancer	Fetal Intestine Large	intestine
47	chr14:36686600-36687200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr14:36686600-36687200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
49	chr14:36686800-36687400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
50	chr14:36686800-36687600	Enhancers	HMEC	breast

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