Variant report

Variant	esv1822009
Chromosome Location	chr15:30372082-30956242
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:4054)
CpG islands
(count:3053)
Chromatin interactive
region (count:3)
LncRNA
region (count:60)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:4054 , 50 per page) page: 1 2 3 4 5 6 7 ... 82

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:30917841-30918381	K562	blood:	n/a	n/a
2	ARID3A	chr15:30917819-30918297	HepG2	liver:	n/a	n/a
3	ARID3A	chr15:30941065-30941323	HepG2	liver:	n/a	chr15:30941184-30941200 chr15:30941198-30941214
4	ATF1	chr15:30917774-30918461	K562	blood:	n/a	n/a
5	ATF1	chr15:30942408-30942747	K562	blood:	n/a	n/a
6	ATF2	chr15:30941959-30942874	GM12878	blood:	n/a	n/a
7	ATF2	chr15:30917694-30918103	GM12878	blood:	n/a	n/a
8	ATF2	chr15:30917709-30918426	GM12878	blood:	n/a	n/a
9	ATF2	chr15:30917808-30918347	H1-hESC	embryonic stem cell:	n/a	n/a
10	ATF2	chr15:30918103-30918425	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF3	chr15:30917703-30918445	A549	lung:	n/a	n/a
12	BACH1	chr15:30396041-30396079	H1-hESC	embryonic stem cell:	n/a	n/a
13	BATF	chr15:30832413-30833670	GM12878	blood:	n/a	chr15:30833063-30833074
14	BATF	chr15:30428014-30428211	GM12878	blood:	n/a	n/a
15	BATF	chr15:30626371-30626674	GM12878	blood:	n/a	chr15:30626595-30626606
16	BATF	chr15:30858799-30859444	GM12878	blood:	n/a	n/a
17	BATF	chr15:30939410-30939698	GM12878	blood:	n/a	n/a
18	BATF	chr15:30389801-30390448	GM12878	blood:	n/a	n/a
19	BATF	chr15:30763589-30764924	GM12878	blood:	n/a	n/a
20	BATF	chr15:30763002-30763213	GM12878	blood:	n/a	n/a
21	BATF	chr15:30402631-30402999	GM12878	blood:	n/a	chr15:30402836-30402847 chr15:30402837-30402847 chr15:30402841-30402851
22	BATF	chr15:30716939-30717383	GM12878	blood:	n/a	n/a
23	BATF	chr15:30717407-30718307	GM12878	blood:	n/a	n/a
24	BATF	chr15:30942101-30942823	GM12878	blood:	n/a	n/a
25	BATF	chr15:30412052-30412331	GM12878	blood:	n/a	n/a
26	BATF	chr15:30678631-30678956	GM12878	blood:	n/a	chr15:30678848-30678858 chr15:30678844-30678854
27	BATF	chr15:30717393-30718193	GM12878	blood:	n/a	n/a
28	BATF	chr15:30871617-30871985	GM12878	blood:	n/a	chr15:30871822-30871833 chr15:30871827-30871837 chr15:30871823-30871833
29	BATF	chr15:30793866-30794121	GM12878	blood:	n/a	n/a
30	BATF	chr15:30939417-30939718	GM12878	blood:	n/a	n/a
31	BATF	chr15:30442191-30442458	GM12878	blood:	n/a	n/a
32	BATF	chr15:30402704-30403029	GM12878	blood:	n/a	chr15:30402836-30402847 chr15:30402837-30402847 chr15:30402841-30402851
33	BATF	chr15:30678661-30679029	GM12878	blood:	n/a	chr15:30678848-30678858 chr15:30678844-30678854
34	BATF	chr15:30459001-30459247	GM12878	blood:	n/a	n/a
35	BATF	chr15:30793879-30794120	GM12878	blood:	n/a	n/a
36	BATF	chr15:30411642-30411805	GM12878	blood:	n/a	n/a
37	BATF	chr15:30829434-30829723	GM12878	blood:	n/a	n/a
38	BATF	chr15:30832414-30833216	GM12878	blood:	n/a	chr15:30833063-30833074
39	BATF	chr15:30763776-30764872	GM12878	blood:	n/a	n/a
40	BATF	chr15:30720885-30721174	GM12878	blood:	n/a	n/a
41	BATF	chr15:30765290-30765504	GM12878	blood:	n/a	n/a
42	BATF	chr15:30942098-30942760	GM12878	blood:	n/a	n/a
43	BATF	chr15:30917720-30918566	GM12878	blood:	n/a	n/a
44	BATF	chr15:30880957-30881265	GM12878	blood:	n/a	n/a
45	BATF	chr15:30411972-30412280	GM12878	blood:	n/a	n/a
46	BATF	chr15:30765283-30765578	GM12878	blood:	n/a	n/a
47	BATF	chr15:30871690-30872015	GM12878	blood:	n/a	chr15:30871822-30871833 chr15:30871827-30871837 chr15:30871823-30871833
48	BATF	chr15:30881037-30881316	GM12878	blood:	n/a	n/a
49	BATF	chr15:30691171-30691739	GM12878	blood:	n/a	n/a
50	BATF	chr15:30626382-30626790	GM12878	blood:	n/a	chr15:30626595-30626606

(count:3053 , 50 per page) page: 1 2 3 4 5 6 7 ... 62

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:30435199-30435249	AoSMC	blood vessel:	n/a
2	chr15:30515844-30515894	ProgFib	skin:	n/a
3	chr15:30517601-30517651	AG09319	gingival:	n/a
4	chr15:30435199-30435249	AoSMC	blood vessel:	n/a
5	chr15:30515844-30515894	ProgFib	skin:	n/a
6	chr15:30517601-30517651	AG09319	gingival:	n/a
7	chr15:30917958-30918008	SK-N-SH	brain:	n/a
8	chr15:30517589-30517639	IMR90	lung:	fetal
9	chr15:30483519-30483569	HCT-116	colon:	n/a
10	chr15:30918313-30918363	HAEpiC	amniotic membrane:	n/a
11	chr15:30816232-30816282	HPAEpiC	pulmonary alveolar:	n/a
12	chr15:30918339-30918389	SK-N-MC	brain:	n/a
13	chr15:30518064-30518114	HPAEpiC	pulmonary alveolar:	n/a
14	chr15:30486767-30486817	ECC-1	luminal epithelium:	n/a
15	chr15:30763199-30763249	NHDF-neo	bronchial:	n/a
16	chr15:30483647-30483697	A549	lung:	n/a
17	chr15:30487914-30487964	AG09319	gingival:	n/a
18	chr15:30515162-30515212	Hela-S3	cervix:	n/a
19	chr15:30483519-30483569	HEEpiC	esophagus:	n/a
20	chr15:30396121-30396171	AG10803	skin:	n/a
21	chr15:30896216-30896266	MCF-7	breast:	n/a
22	chr15:30918595-30918645	NHDF-neo	bronchial:	n/a
23	chr15:30844060-30844110	SK-N-SH	brain:	n/a
24	chr15:30487914-30487964	HAEpiC	amniotic membrane:	n/a
25	chr15:30865191-30865241	GM12878	blood:	n/a
26	chr15:30699977-30700027	U87	brain:	n/a
27	chr15:30918339-30918389	HNPCEpiC	eye:	n/a
28	chr15:30515162-30515212	SK-N-SH_RA	brain:	n/a
29	chr15:30763487-30763537	NH-A	brain:	n/a
30	chr15:30487914-30487964	SKMC	muscle:	n/a
31	chr15:30517601-30517651	NH-A	brain:	n/a
32	chr15:30520018-30520068	GM12891	blood:	n/a
33	chr15:30483647-30483697	MCF10A-Er-Src	breast:	n/a
34	chr15:30518064-30518114	BE2_C	brain:	n/a
35	chr15:30865191-30865241	HRE	kidney:	n/a
36	chr15:30896216-30896266	Hela-S3	cervix:	n/a
37	chr15:30434661-30434711	HMEC	breast:	n/a
38	chr15:30919020-30919070	AG04449	skin:	fetal
39	chr15:30520018-30520068	HCT-116	colon:	n/a
40	chr15:30489014-30489064	PFSK-1	brain:	n/a
41	chr15:30700112-30700162	Jurkat	blood:	n/a
42	chr15:30865200-30865250	GM12878	blood:	n/a
43	chr15:30917918-30917968	HCT-116	colon:	n/a
44	chr15:30917991-30918041	GM12892	blood:	n/a
45	chr15:30763199-30763249	HRCEpiC	kidney:	n/a
46	chr15:30699977-30700027	PFSK-1	brain:	n/a
47	chr15:30517601-30517651	HCPEpiC	choroid plexus:	n/a
48	chr15:30763199-30763249	HCPEpiC	choroid plexus:	n/a
49	chr15:30486767-30486817	ovcar-3	ovarian:	n/a
50	chr15:30483519-30483569	SAEC	small airway:	n/a

(count:3 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:30918095..30918834-chr2:231728599..231729465,2	Hela-S3	cervix:
2	chr15:30916698..30918883-chr15:32905767..32907284,2	MCF-7	breast:
3	chr15:30917826..30919798-chr15:32905900..32908033,2	K562	blood:

(count:60 , 50 per page) page: 1 2

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CHRNA7-2	chr15:30888863-30888941	NONHSAT041366
2	lnc-RP11-382B18.2.1-2	chr15:30675522-30675585	NONHSAT041347
3	lnc-CHRFAM7A-2	chr15:30649969-30650976	ENSG00000270173.1
4	lnc-CHRNA7-2	chr15:30888863-30889187	NONHSAT041367
5	lnc-RP11-382B18.2.1-1	chr15:30917254-30917976	ENSG00000247728.2
6	lnc-CHRFAM7A-1	chr15:30462912-30462975	ENSG00000259906.1
7	lnc-CHRNA7-2	chr15:30878081-30878127	NONHSAT041368
8	lnc-CHRFAM7A-1	chr15:30471212-30471332	ENSG00000259906.1
9	lnc-RP11-382B18.2.1-2	chr15:30673906-30674079	NONHSAT041347
10	lnc-AC120045.3-2	chr15:30435925-30436203	NONHSAT041332
11	lnc-GOLGA8H-1	chr15:30909161-30909952	ENSG00000269930.1
12	lnc-AC026150.9.1-5	chr15:30702037-30703662	NONHSAT041356
13	lnc-ARHGAP11B-1	chr15:30916697-30916815	NONHSAT041376
14	lnc-CHRNA7-2	chr15:30892305-30892850	NONHSAT140224
15	lnc-CHRNA7-2	chr15:30871491-30871615	NONHSAT041366
16	lnc-ARHGAP11B-2	chr15:30904916-30905194	NONHSAT041372
17	lnc-RP5-1086D14.3.1-1	chr15:30491478-30491534	ENSG00000225930.3
18	lnc-RP11-382B18.2.1-1	chr15:30917254-30917976	ENSG00000247728
19	lnc-GOLGA8H-2	chr15:30941000-30941732	ENSG00000269974.1
20	lnc-AC026150.9.1-3	chr15:30780166-30782516	ENSG00000270055.1
21	lnc-CHRNA7-2	chr15:30888863-30888941	NONHSAT140224
22	lnc-RP11-382B18.2.1-1	chr15:30857143-30857384	ENSG00000247728
23	lnc-RP5-1086D14.3.1-1	chr15:30502620-30506743	ENSG00000225930.3
24	lnc-CHRNA7-2	chr15:30892305-30892900	NONHSAT041368
25	lnc-CHRNA7-2	chr15:30892305-30892911	NONHSAT041366
26	lnc-ARHGAP11B-1	chr15:30917557-30918469	NONHSAT041376
27	lnc-AC026150.9.1-1	chr15:30836768-30836863	ENSG00000260693.1
28	lnc-RP11-382B18.2.1-2	chr15:30672556-30672602	NONHSAT041347
29	lnc-CHRFAM7A-1	chr15:30462766-30462831	ENSG00000259906.1
30	lnc-CHRNA7-2	chr15:30865172-30865219	NONHSAT041368
31	lnc-CHRFAM7A-3	chr15:30697514-30697792	NONHSAT041354
32	lnc-RP11-382B18.2.1-3	chr15:30899898-30900396	ENSG00000270016.1
33	lnc-CHRNA7-2	chr15:30865172-30865219	NONHSAT140224
34	lnc-CHRNA7-2	chr15:30871491-30871615	NONHSAT041368
35	lnc-CHRNA7-2	chr15:30871491-30871615	NONHSAT140224
36	lnc-RP5-1086D14.3.1-1	chr15:30488239-30488317	ENSG00000225930.3
37	lnc-RP5-1086D14.3.1-1	chr15:30488239-30488317	ENSG00000225930.2
38	lnc-RP11-382B18.2.1-1	chr15:30909201-30909447	ENSG00000247728.2
39	lnc-RP5-1086D14.3.1-1	chr15:30502620-30504471	ENSG00000225930.2
40	lnc-CHRNA7-2	chr15:30864758-30864774	NONHSAT041366
41	lnc-RP11-382B18.2.1-2	chr15:30679066-30679190	NONHSAT041348
42	lnc-RP5-1086D14.3.1-1	chr15:30491478-30491534	ENSG00000225930.2
43	lnc-AC026150.9.1-1	chr15:30838015-30838172	ENSG00000260693.1
44	lnc-ARHGAP11B-1	chr15:30916926-30917019	NONHSAT041376
45	lnc-CHRNA7-2	chr15:30865088-30865219	NONHSAT041367
46	lnc-RP11-382B18.2.1-2	chr15:30675247-30675585	NONHSAT041348
47	lnc-CHRNA7-2	chr15:30865172-30865219	NONHSAT041366
48	lnc-CHRNA7-2	chr15:30871491-30871615	NONHSAT041367
49	lnc-RP11-382B18.2.1-2	chr15:30679087-30679190	NONHSAT041347
50	lnc-CHRFAM7A-1	chr15:30471079-30472146	ENSG00000259906.1

No data

Variant related genes	Relation type
ENSG00000221593	TF binding region
ENSG00000207430	TF binding region
RN7SL196P	TF binding region
RN7SL628P	TF binding region
GOLGA8H	TF binding region
ULK4P3	TF binding region
ARHGAP11B	TF binding region
RNU6-17P	TF binding region
ENSG00000247728	TF binding region
RN7SL469P	TF binding region
ENSG00000238519	TF binding region
ENSG00000260693	TF binding region
GOLGA8R	TF binding region
RN7SL796P	TF binding region
DNM1P50	TF binding region
ENSG00000238783	TF binding region
ENSG00000263070	TF binding region
ENSG00000225930	TF binding region
ENSG00000260784	TF binding region
ENSG00000270173	TF binding region
ENSG00000252602	TF binding region
ENSG00000271333	TF binding region
ENSG00000215302	TF binding region
ENSG00000221785	TF binding region
CHRFAM7A	TF binding region
ENSG00000261747	TF binding region
ENSG00000221250	TF binding region
ENSG00000270016	TF binding region
ENSG00000221723	TF binding region
ENSG00000207432	TF binding region
RN7SL673P	TF binding region
ULK4P2	TF binding region
GOLGA8T	TF binding region
DNM1P30	TF binding region
ENSG00000269930	TF binding region
ENSG00000269974	TF binding region
ENSG00000259906	TF binding region
ENSG00000270055	TF binding region
GOLGA8J	TF binding region
DNM1P28	TF binding region
ENSG00000270955	TF binding region
ENSG00000221358	TF binding region
ENSG00000259993	TF binding region
GOLGA8Q	TF binding region
ENSG00000221593	CpG island
ENSG00000207430	CpG island
RN7SL196P	CpG island
RN7SL628P	CpG island
GOLGA8H	CpG island
ULK4P3	CpG island
ARHGAP11B	CpG island
RNU6-17P	CpG island
ENSG00000247728	CpG island
RN7SL469P	CpG island
ENSG00000238519	CpG island
ENSG00000260693	CpG island
GOLGA8R	CpG island
RN7SL796P	CpG island
DNM1P50	CpG island
ENSG00000238783	CpG island
ENSG00000263070	CpG island
ENSG00000225930	CpG island
ENSG00000260784	CpG island
ENSG00000270173	CpG island
ENSG00000252602	CpG island
ENSG00000271333	CpG island
ENSG00000215302	CpG island
ENSG00000221785	CpG island
CHRFAM7A	CpG island
ENSG00000261747	CpG island
ENSG00000221250	CpG island
ENSG00000270016	CpG island
ENSG00000221723	CpG island
ENSG00000207432	CpG island
RN7SL673P	CpG island
ULK4P2	CpG island
GOLGA8T	CpG island
DNM1P30	CpG island
ENSG00000269930	CpG island
ENSG00000269974	CpG island
ENSG00000259906	CpG island
ENSG00000270055	CpG island
GOLGA8J	CpG island
DNM1P28	CpG island
ENSG00000270955	CpG island
ENSG00000221358	CpG island
ENSG00000259993	CpG island
GOLGA8Q	CpG island
ENSG00000198826	chromatin interactions
ENSG00000135916	chromatin interactions
ENSG00000262728	chromatin interactions
ENSG00000244952	chromatin interactions
PRKAB2	miRNA target sites
TGFB2	miRNA target sites

Extended variants
information (count: 4353 )
Associated
traits (count: 150 )

Variant overlapped rSNPs/rCNVs (count:4353 , 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	rs545034671	chr15:30372087-30372088	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs560104945	chr15:30372095-30372096	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs577403856	chr15:30372098-30372099	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs191258211	chr15:30372120-30372121	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs553579446	chr15:30372121-30372122	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs572990468	chr15:30372124-30372125	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs143872044	chr15:30372149-30372150	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs561539257	chr15:30372155-30372156	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs530422477	chr15:30372158-30372159	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs531775170	chr15:30372193-30372194	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs373558291	chr15:30372197-30372198	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs544533981	chr15:30372204-30372205	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs183219137	chr15:30372251-30372252	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs550468725	chr15:30372256-30372257	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs369691518	chr15:30372259-30372260	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs539334207	chr15:30372267-30372268	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs546410665	chr15:30372282-30372283	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs566294558	chr15:30372313-30372314	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs150609807	chr15:30372319-30372320	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs528570716	chr15:30372357-30372358	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs548344830	chr15:30372364-30372365	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs568486949	chr15:30372413-30372414	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs202085516	chr15:30372426-30372427	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs537037807	chr15:30372438-30372439	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs4275831	chr15:30372459-30372460	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs199975592	chr15:30372463-30372464	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs4448915	chr15:30372466-30372467	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs7176620	chr15:30372473-30372474	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs573427971	chr15:30372475-30372476	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs9708145	chr15:30372480-30372481	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs7177988	chr15:30372495-30372496	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs544898267	chr15:30372502-30372503	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs200341648	chr15:30372505-30372506	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs12592895	chr15:30372512-30372513	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs146760384	chr15:30372517-30372518	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs372260511	chr15:30372555-30372556	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs572066160	chr15:30372556-30372557	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs74011040	chr15:30372571-30372572	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs74011041	chr15:30372573-30372574	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs192147507	chr15:30372606-30372607	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs529048556	chr15:30372612-30372613	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs201720145	chr15:30372618-30372619	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs71397299	chr15:30372653-30372654	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs140663819	chr15:30372697-30372698	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs531009005	chr15:30372721-30372722	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs550717693	chr15:30372726-30372727	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs570822494	chr15:30372727-30372728	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs150115085	chr15:30372738-30372739	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs185077074	chr15:30372751-30372752	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs4587953	chr15:30372763-30372764	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:150)

Disease	PMID	Source
Ovarian cancer	21720365	CNVD
HDAC8	0	CNVD
NIPBL	0	CNVD
RAD21	0	CNVD
SMC1A	0	CNVD
SMC3	0	CNVD
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Prader-willi syndrome	21504564	CNVD
The inv dup or idic syndrome	19019226	CNVD
Prader-willi syndrome	21233802	CNVD
Angelman syndrome	16617304	CNVD
Angelman syndrome	20970697	CNVD
Autism	22958593	CNVD
Prader-willi syndrome	16617304	CNVD
Prader-willi syndrome	18923514	CNVD
Prader-willi syndrome	20970697	CNVD
Angelman syndrome	16183798	CNVD
Angelman syndrome	18923514	CNVD
Prader-willi syndrome	22241247	CNVD
Epilepsy	20970697	CNVD
Autism	20970697	CNVD
Autism	19935738	CNVD
Autism	22930557	CNVD
Autism	19966786	CNVD
Autism	18923514	CNVD
Autism	18925931	CNVD
Autism	18835857	CNVD
Prader-willi syndrome	18835857	CNVD
Prader-willi syndrome	22152151	CNVD
Autism	22241247	CNVD
15q-syndrome	21725066	CNVD
Prader-willi syndrome	21503198	CNVD
Autism	21956041	CNVD
Prader-willi syndrome	16760730	CNVD
Prader-willi syndrome	22470819	CNVD
prenatal diagnosis	20453657	CNVD
Prader-willi syndrome	17867985	CNVD
Angelman syndrome	21072004	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Testicular germ cell tumor	18059402	CNVD
cataract	16735990	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Medulloblastoma	21979893	CNVD
spastic paraplegia with thinning of corpus callosum	19105190	CNVD
Schizophrenia	21324950	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Disease	21824424	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Prader-willi syndrome	18781185	CNVD
Melanoma	18172304	CNVD
Autism	17322880	CNVD
Prader-willi syndrome	19329560	CNVD
Autism	17999366	CNVD
Autism	17901113	CNVD
Neurodevelopmental disorder	17015230	CNVD
Autism	18414403	CNVD
Neurocytoma	17123091	CNVD
Mental retardation	18923513	CNVD
Colorectal cancer	16774939	CNVD
Gastric cancer	17167181	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Colorectal cancer	16272173	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Multiple myeloma	17550852	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Intellectual disability	22102821	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	20729466	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Breast cancer	17133270	CNVD
Prostate cancer	16573809	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Multiple myeloma	20724749	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21785460	CNVD
Prostate cancer	18632612	CNVD
Angelman syndrome	18787571	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Abnormal corpus callosum	21572526	CNVD
idiopathic generalized epilepsy	19843651	CNVD
Autism	20531469	CNVD
Neuropsychiatric disorder	20506139	CNVD
Austim spectrum disorder	21302340	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Autism	19204725	CNVD
Schizophrenia	19204725	CNVD
Schizophrenia	19149910	CNVD
Schizophrenia	20967226	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Autism	22543975	CNVD
Epilepsy	22499536	CNVD
Schizophrenia	22499536	CNVD
Schizophrenia	18923514	CNVD
Bipolar disorder	19114987	CNVD
Schizophrenia	20587603	CNVD
Schizophrenia	22958593	CNVD
Schizophrenia	21285140	CNVD
Schizophrenia	20553308	CNVD
Schizophrenia	21956041	CNVD
Schizophrenia	20970697	CNVD
Mental retardation	19951919	CNVD
Mental retardation	21956041	CNVD
Myelofibrosis	22110671	CNVD
Mental retardation	21062444	CNVD
Autism	21269290	CNVD
Intellectual disability	21269290	CNVD
Schizophrenia	21269290	CNVD
Colorectal cancer	21128281	CNVD
Epilepsy	19289393	CNVD
Epilepsy	20643615	CNVD
Mental retardation	19289393	CNVD
Mental retardation	20152051	CNVD
Schizophrenia	19289393	CNVD
dysmorphic features	19289393	CNVD
idiopathic epilepsies	19341504	CNVD
idiopathic generalized epilepsy	19592580	CNVD
idiopathic generalized epilepsy	19136953	CNVD
Autism	22094647	CNVD
Developmental delay	19898479	CNVD
Mental retardation	18278044	CNVD
Mental retardation	19898479	CNVD
Prader-willi syndrome	18854863	CNVD
Schizophrenia	19855392	CNVD
Ovarian cancer	22174824	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Cancer	20164919	CNVD
small cell lung cancer	20016488	CNVD
Epilepsy	20502679	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Intellectual disability	21811512	CNVD
Glioma	20126413	CNVD

Chromatin state (count:1394 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:30367600-30372600	Weak transcription	HSMM	muscle
2	chr15:30372600-30372800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
3	chr15:30372600-30373000	Enhancers	HSMM	muscle
4	chr15:30372600-30373600	Enhancers	Muscle Satellite Cultured Cells	--
5	chr15:30372800-30373400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
6	chr15:30372800-30373600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
7	chr15:30373200-30373400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
8	chr15:30373200-30373400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr15:30373200-30373400	Enhancers	HSMMtube	muscle
10	chr15:30373200-30373400	Enhancers	Osteobl	bone
11	chr15:30395800-30396000	Active TSS	HMEC	breast
12	chr15:30395800-30396200	Active TSS	Primary neutrophils fromperipheralblood	blood
13	chr15:30395800-30396200	Active TSS	Primary B cells from peripheral blood	blood
14	chr15:30395800-30396200	Active TSS	Colonic Mucosa	Colon
15	chr15:30395800-30396200	Active TSS	Gastric	stomach
16	chr15:30395800-30396400	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr15:30395800-30396400	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
18	chr15:30395800-30396400	Active TSS	HUES48 Cell Line	embryonic stem cell
19	chr15:30395800-30396400	Active TSS	Breast Myoepithelial Primary Cells	Breast
20	chr15:30395800-30396400	Active TSS	Muscle Satellite Cultured Cells	--
21	chr15:30395800-30396400	Active TSS	Cortex derived primary cultured neurospheres	brain
22	chr15:30395800-30396400	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
23	chr15:30395800-30396400	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
24	chr15:30395800-30396400	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
25	chr15:30395800-30396400	Active TSS	Adipose Nuclei	Adipose
26	chr15:30395800-30396400	Active TSS	Esophagus	oesophagus
27	chr15:30395800-30396400	Active TSS	Fetal Brain Female	brain
28	chr15:30395800-30396400	Bivalent/Poised TSS	Fetal Stomach	stomach
29	chr15:30395800-30396400	Active TSS	Left Ventricle	heart
30	chr15:30395800-30396400	Active TSS	Rectal Mucosa Donor 31	rectum
31	chr15:30395800-30396400	Active TSS	Right Atrium	heart
32	chr15:30395800-30396400	Active TSS	Right Ventricle	heart
33	chr15:30395800-30396400	Active TSS	Thymus	Thymus
34	chr15:30395800-30396400	Active TSS	Spleen	Spleen
35	chr15:30395800-30396400	Active TSS	HepG2	liver
36	chr15:30395800-30396400	Active TSS	Monocytes-CD14+_RO01746	blood
37	chr15:30395800-30396600	Active TSS	H1 Cell Line	embryonic stem cell
38	chr15:30395800-30396600	Active TSS	HUES6 Cell Line	embryonic stem cell
39	chr15:30395800-30396600	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
40	chr15:30395800-30396600	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
41	chr15:30395800-30396600	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
42	chr15:30395800-30396600	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
43	chr15:30395800-30396600	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
44	chr15:30395800-30396600	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
45	chr15:30395800-30396600	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
46	chr15:30395800-30396600	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
47	chr15:30395800-30396600	Active TSS	Pancreas	Pancrea
48	chr15:30395800-30396600	Active TSS	HUVEC	blood vessel
49	chr15:30395800-30396800	Active TSS	HUES64 Cell Line	embryonic stem cell
50	chr15:30395800-30396800	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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