Variant report

Variant	esv2760046
Chromosome Location	chr15:82879646-83310525
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:5535)
CpG islands
(count:1650)
Chromatin interactive
region (count:106)
LncRNA
region (count:29)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:5535 , 50 per page) page: 1 2 3 4 5 6 7 ... 111

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:83235552-83235633	K562	blood:	n/a	n/a
2	ARID3A	chr15:83304545-83304986	K562	blood:	n/a	n/a
3	ARID3A	chr15:83253994-83254167	K562	blood:	n/a	n/a
4	ATF1	chr15:83217686-83218291	K562	blood:	n/a	n/a
5	ATF1	chr15:83235535-83235751	K562	blood:	n/a	n/a
6	ATF1	chr15:82944794-82944809	K562	blood:	n/a	n/a
7	ATF1	chr15:83309450-83309802	K562	blood:	n/a	n/a
8	ATF2	chr15:83220501-83221054	GM12878	blood:	n/a	n/a
9	ATF3	chr15:83253894-83254181	K562	blood:	n/a	n/a
10	ATF3	chr15:83235461-83235792	K562	blood:	n/a	n/a
11	BACH1	chr15:83238742-83238834	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr15:83234712-83234930	H1-hESC	embryonic stem cell:	n/a	n/a
13	BATF	chr15:83023136-83023728	GM12878	blood:	n/a	n/a
14	BATF	chr15:83011645-83011979	GM12878	blood:	n/a	n/a
15	BATF	chr15:83194668-83194970	GM12878	blood:	n/a	n/a
16	BATF	chr15:82993347-82993563	GM12878	blood:	n/a	n/a
17	BATF	chr15:83094172-83094396	GM12878	blood:	n/a	n/a
18	BATF	chr15:82932684-82933018	GM12878	blood:	n/a	n/a
19	BATF	chr15:82939214-82939411	GM12878	blood:	n/a	n/a
20	BATF	chr15:83024410-83024664	GM12878	blood:	n/a	n/a
21	BATF	chr15:83163774-83163970	GM12878	blood:	n/a	n/a
22	BATF	chr15:83113978-83114251	GM12878	blood:	n/a	n/a
23	BATF	chr15:82951589-82951845	GM12878	blood:	n/a	chr15:82951597-82951605
24	BATF	chr15:82946619-82946832	GM12878	blood:	n/a	n/a
25	BATF	chr15:82932666-82932968	GM12878	blood:	n/a	n/a
26	BATF	chr15:83104579-83104871	GM12878	blood:	n/a	n/a
27	BATF	chr15:82945410-82945664	GM12878	blood:	n/a	n/a
28	BATF	chr15:83188292-83188489	GM12878	blood:	n/a	n/a
29	BATF	chr15:83104587-83104871	GM12878	blood:	n/a	n/a
30	BATF	chr15:83122080-83122266	GM12878	blood:	n/a	n/a
31	BATF	chr15:83209109-83209373	GM12878	blood:	n/a	n/a
32	BATF	chr15:83001027-83001250	GM12878	blood:	n/a	n/a
33	BATF	chr15:82946030-82946597	GM12878	blood:	n/a	n/a
34	BATF	chr15:83050183-83050497	GM12878	blood:	n/a	n/a
35	BATF	chr15:83181094-83181867	GM12878	blood:	n/a	n/a
36	BATF	chr15:83025030-83025597	GM12878	blood:	n/a	n/a
37	BATF	chr15:83199520-83199738	GM12878	blood:	n/a	n/a
38	BATF	chr15:83217478-83217841	GM12878	blood:	n/a	n/a
39	BATF	chr15:83108862-83109197	GM12878	blood:	n/a	n/a
40	BATF	chr15:82947458-82947719	GM12878	blood:	n/a	n/a
41	BATF	chr15:82994132-82994379	GM12878	blood:	n/a	n/a
42	BATF	chr15:83181297-83181619	GM12878	blood:	n/a	n/a
43	BATF	chr15:83129049-83129439	GM12878	blood:	n/a	n/a
44	BATF	chr15:83113516-83113715	GM12878	blood:	n/a	n/a
45	BATF	chr15:83182024-83182278	GM12878	blood:	n/a	n/a
46	BATF	chr15:83002651-83002988	GM12878	blood:	n/a	n/a
47	BATF	chr15:83002686-83002927	GM12878	blood:	n/a	n/a
48	BATF	chr15:83018215-83018412	GM12878	blood:	n/a	n/a
49	BATF	chr15:83206289-83206581	GM12878	blood:	n/a	n/a
50	BATF	chr15:83115167-83115390	GM12878	blood:	n/a	n/a

(count:1650 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:83166174-83166224	GM12892	blood:	n/a
2	chr15:83240633-83240683	HCM	heart:	n/a
3	chr15:83026317-83026367	NH-A	brain:	n/a
4	chr15:83166174-83166224	GM12892	blood:	n/a
5	chr15:83240633-83240683	HCM	heart:	n/a
6	chr15:83026317-83026367	NH-A	brain:	n/a
7	chr15:83240213-83240263	Hela-S3	cervix:	n/a
8	chr15:83225358-83225408	ovcar-3	ovarian:	n/a
9	chr15:83241300-83241350	HCF	heart:	n/a
10	chr15:83226219-83226269	A549	lung:	n/a
11	chr15:83255558-83255608	GM12892	blood:	n/a
12	chr15:83300338-83300388	HEEpiC	esophagus:	n/a
13	chr15:82944254-82944304	BE2_C	brain:	n/a
14	chr15:83002290-83002340	GM12878	blood:	n/a
15	chr15:82925333-82925383	HepG2	liver:	n/a
16	chr15:83240213-83240263	PANC-1	pancreas:	n/a
17	chr15:83241300-83241350	MCF-7	breast:	n/a
18	chr15:82959442-82959492	PANC-1	pancreas:	n/a
19	chr15:83298692-83298742	RPTEC	kidney:	n/a
20	chr15:82944254-82944304	HRCEpiC	kidney:	n/a
21	chr15:83241300-83241350	GM12891	blood:	n/a
22	chr15:82915331-82915381	AG09319	gingival:	n/a
23	chr15:83241300-83241350	NHBE	bronchial:	n/a
24	chr15:82944254-82944304	SAEC	small airway:	n/a
25	chr15:82959442-82959492	HCM	heart:	n/a
26	chr15:82944254-82944304	K562	blood:	n/a
27	chr15:83239908-83239958	SK-N-MC	brain:	n/a
28	chr15:83002290-83002340	U87	brain:	n/a
29	chr15:83300338-83300388	LNCaP	prostate:	n/a
30	chr15:83298692-83298742	HUVEC	blood vessel:	n/a
31	chr15:83240213-83240263	SK-N-SH	brain:	n/a
32	chr15:83240633-83240683	NHBE	bronchial:	n/a
33	chr15:83240213-83240263	NT2-D1	testis:	n/a
34	chr15:83002290-83002340	HNPCEpiC	eye:	n/a
35	chr15:83240213-83240263	LNCaP	prostate:	n/a
36	chr15:83240693-83240743	HMEC	breast:	n/a
37	chr15:83241867-83241917	MCF-7	breast:	n/a
38	chr15:83240550-83240600	H1-hESC	embryonic stem cell:	embryo
39	chr15:82915331-82915381	HRPEpiC	eye:	n/a
40	chr15:83226580-83226630	HCT-116	colon:	n/a
41	chr15:83239908-83239958	HEEpiC	esophagus:	n/a
42	chr15:83226580-83226630	AG10803	skin:	n/a
43	chr15:83240213-83240263	GM19239	blood:	n/a
44	chr15:83240633-83240683	HUVEC	blood vessel:	n/a
45	chr15:83240633-83240683	CMK	blood:	n/a
46	chr15:83240550-83240600	SK-N-SH_RA	brain:	n/a
47	chr15:83240213-83240263	T-47D	breast:	n/a
48	chr15:83225358-83225408	BE2_C	brain:	n/a
49	chr15:82959442-82959492	HNPCEpiC	eye:	n/a
50	chr15:83026317-83026367	PFSK-1	brain:	n/a

(count:106 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr15:83217765..83219665-chr15:83228669..83230495,2	K562	blood:
2	chr15:83216641..83218294-chr15:83221044..83223302,2	K562	blood:
3	chr15:83273498..83275369-chr15:83275649..83277531,2	MCF-7	breast:
4	chr15:83212827..83216127-chr15:83234244..83236895,3	MCF-7	breast:
5	chr15:83213257..83215653-chr15:83219949..83222640,2	K562	blood:
6	chr15:83288307..83289811-chr15:83295529..83297822,2	K562	blood:
7	chr15:83293051..83295110-chr15:83315019..83317185,2	K562	blood:
8	chr15:83229777..83231683-chr15:83417698..83419627,2	K562	blood:
9	chr15:83212827..83216127-chr15:83234244..83236895,3	MCF-7	breast:
10	chr15:83223012..83224656-chr15:83233813..83235833,2	K562	blood:
11	chr15:83229558..83232531-chr15:83236614..83238235,2	K562	blood:
12	chr15:83254839..83257553-chr15:83348845..83350851,2	MCF-7	breast:
13	chr15:83226594..83230690-chr15:83232358..83235260,6	K562	blood:
14	chr15:83216717..83218665-chr15:83313410..83315739,2	K562	blood:
15	chr15:83267772..83269526-chr15:83272554..83274146,2	K562	blood:
16	chr15:83233152..83235673-chr15:83264929..83267672,2	MCF-7	breast:
17	chr15:83233152..83235673-chr15:83264929..83267672,2	MCF-7	breast:
18	chr15:83222088..83224291-chr15:83225999..83227759,2	MCF-7	breast:
19	chr15:83227977..83230021-chr15:83296257..83298165,2	K562	blood:
20	chr15:83217263..83220611-chr15:83348215..83350818,3	MCF-7	breast:
21	chr15:83253377..83255551-chr15:83668447..83670798,2	MCF-7	breast:
22	chr15:83261732..83263862-chr15:83266441..83269170,2	MCF-7	breast:
23	chr15:83237529..83239820-chr15:83240454..83244037,3	MCF-7	breast:
24	chr15:83250683..83253027-chr15:83273825..83276557,2	K562	blood:
25	chr15:83214650..83216345-chr15:83216963..83219533,2	K562	blood:
26	chr15:83238616..83241494-chr15:83254694..83256457,2	MCF-7	breast:
27	chr15:83217765..83219665-chr15:83228669..83230495,2	K562	blood:
28	chr15:83267772..83269526-chr15:83272554..83274146,2	K562	blood:
29	chr15:83290643..83294390-chr15:83347745..83350836,4	MCF-7	breast:
30	chr15:83258007..83260453-chr15:83266381..83268197,2	K562	blood:
31	chr15:83233938..83235753-chr15:83244078..83245839,2	K562	blood:
32	chr15:83218421..83221235-chr15:83235743..83238150,2	K562	blood:
33	chr15:83233945..83235595-chr15:83736586..83738485,2	K562	blood:
34	chr15:83286159..83288277-chr15:83291289..83293373,3	K562	blood:
35	chr15:83276398..83279103-chr15:83299744..83301374,2	K562	blood:
36	chr15:83234815..83238335-chr15:83239517..83241616,4	K562	blood:
37	chr15:83217723..83220183-chr15:83220219..83222791,2	K562	blood:
38	chr15:83290172..83292221-chr15:83420651..83422784,2	MCF-7	breast:
39	chr15:83293051..83295658-chr15:83314661..83316519,2	K562	blood:
40	chr15:83289605..83293434-chr15:83349009..83350670,4	MCF-7	breast:
41	chr15:83222033..83224471-chr15:83230402..83232707,2	MCF-7	breast:
42	chr15:83217974..83220864-chr15:83234820..83237093,3	MCF-7	breast:
43	chr15:83254004..83256301-chr15:83611241..83613482,2	MCF-7	breast:
44	chr15:83225038..83226664-chr15:83226825..83228922,2	MCF-7	breast:
45	chr15:83304208..83306459-chr15:83417486..83420687,3	K562	blood:
46	chr15:83292844..83294739-chr15:83312087..83314225,2	K562	blood:
47	chr15:83223012..83224656-chr15:83233813..83235833,2	K562	blood:
48	chr15:83226594..83229969-chr15:83232358..83234992,5	K562	blood:
49	chr15:83296579..83300038-chr15:83302412..83305627,3	K562	blood:
50	chr15:83230372..83232700-chr15:83234500..83237341,4	MCF-7	breast:

(count:29 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AP3B2-2	chr15:83309408-83309616	NONHSAT047840
2	lnc-AP3B2-2	chr15:83310376-83310433	NONHSAT047840
3	lnc-RP13-996F3.5.1-1	chr15:82936963-82937350	NONHSAT047801
4	lnc-RP13-996F3.5.1-2	chr15:83015964-83016351	NONHSAT047817
5	lnc-CPEB1-1	chr15:83296040-83296118	NONHSAT047839
6	lnc-RP11-152F13.5.1-1	chr15:83088710-83088805	ENSG00000259310.1
7	lnc-RP13-996F3.5.1-2	chr15:83018015-83018160	NONHSAT047817
8	lnc-AP3B2-2	chr15:83307316-83307385	NONHSAT047840
9	lnc-RP11-152F13.5.1-1	chr15:83101543-83101623	ENSG00000259310.1
10	lnc-RP11-152F13.5.1-1	chr15:83100556-83100943	NONHSAT047821
11	lnc-RP13-996F3.5.1-1	chr15:82939014-82939159	NONHSAT047801
12	lnc-RP11-152F13.5.1-1	chr15:83098748-83098893	NONHSAT047821
13	lnc-RP11-152F13.5.1-1	chr15:83100556-83100675	ENSG00000259310.1
14	lnc-RP11-379H8.1.1-3	chr15:83293111-83293510	l_1205_chr15:83293110-83297075_liver
15	lnc-RP11-152F13.5.1-1	chr15:83088098-83088121	NONHSAT047819
16	lnc-RP11-152F13.5.1-1	chr15:83101302-83101357	ENSG00000259310.1
17	lnc-RP11-152F13.5.1-1	chr15:83083411-83083534	NONHSAT140250
18	lnc-RP11-152F13.5.1-3	chr15:82969419-82969698	NONHSAT047808
19	lnc-RPS17L-1	chr15:83146764-83147043	NONHSAT047830
20	lnc-RP11-152F13.5.1-1	chr15:83102759-83102960	ENSG00000259310.1
21	lnc-RP11-152F13.5.1-1	chr15:83084257-83084405	NONHSAT047819
22	lnc-RP11-379H8.1.1-3	chr15:83295315-83295451	l_1205_chr15:83293110-83297075_liver
23	lnc-RP11-152F13.5.1-1	chr15:83087381-83087522	ENSG00000259310.1
24	lnc-RP11-152F13.5.1-1	chr15:83102288-83102375	ENSG00000259310.1
25	lnc-RP11-152F13.5.1-1	chr15:83087366-83087522	NONHSAT047819
26	lnc-RP11-379H8.1.1-3	chr15:83296489-83297075	l_1205_chr15:83293110-83297075_liver
27	lnc-RP11-152F13.5.1-1	chr15:83084258-83084733	NONHSAT140250
28	lnc-AP3B2-2	chr15:83301933-83301972	NONHSAT047840
29	lnc-RP11-152F13.5.1-1	chr15:83087938-83087977	NONHSAT047819

No data

Variant related genes	Relation type
RN7SL256P	TF binding region
ENSG00000259310	TF binding region
CPEB1	TF binding region
RPL9P8	TF binding region
CSPG4P9	TF binding region
ADAMTS7P2	TF binding region
UBE2Q2P3	TF binding region
ENSG00000259323	TF binding region
ENSG00000259328	TF binding region
ENSG00000260836	TF binding region
DNM1P42	TF binding region
RN7SL410P	TF binding region
ENSG00000221177	TF binding region
CSPG4P10	TF binding region
GOLGA6L18	TF binding region
ENSG00000261086	TF binding region
ENSG00000259472	TF binding region
GOLGA6L19	TF binding region
RPS17L	TF binding region
GOLGA6L21P	TF binding region
ENSG00000221517	TF binding region
GOLGA6L20	TF binding region
RN7SL256P	CpG island
ENSG00000259310	CpG island
CPEB1	CpG island
RPL9P8	CpG island
CSPG4P9	CpG island
ADAMTS7P2	CpG island
UBE2Q2P3	CpG island
ENSG00000259323	CpG island
ENSG00000259328	CpG island
ENSG00000260836	CpG island
DNM1P42	CpG island
RN7SL410P	CpG island
ENSG00000221177	CpG island
CSPG4P10	CpG island
GOLGA6L18	CpG island
ENSG00000261086	CpG island
ENSG00000259472	CpG island
GOLGA6L19	CpG island
RPS17L	CpG island
GOLGA6L21P	CpG island
ENSG00000221517	CpG island
GOLGA6L20	CpG island
ENSG00000260836	chromatin interactions
ENSG00000252690	chromatin interactions
ENSG00000250988	chromatin interactions
ENSG00000214575	chromatin interactions
ENSG00000103723	chromatin interactions
ENSG00000259462	chromatin interactions

Extended variants
information (count: 4172 )
Associated
traits (count: 76 )

Variant overlapped rSNPs/rCNVs (count:4172 , 50 per page) page: 1 2 3 4 5 6 7 ... 84

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs113095946	chr15:82884986-82884987	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs112102822	chr15:82885148-82885149	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs142945644	chr15:82885151-82885152	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs2695713	chr15:82941058-82941059	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
5	rs140879168	chr15:82943523-82943524	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
6	rs200093204	chr15:82943733-82943734	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
7	rs113206471	chr15:82944329-82944330	Active TSS Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
8	rs539366409	chr15:82945671-82945672	Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs112055686	chr15:82945697-82945698	Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs181074183	chr15:82945748-82945749	Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs373657694	chr15:82945775-82945776	Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs375902415	chr15:82959184-82959185	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs202056082	chr15:82959188-82959189	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs368604452	chr15:82959222-82959223	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs76352111	chr15:82959234-82959235	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs75554775	chr15:82959244-82959245	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs569198699	chr15:82959245-82959246	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs80185306	chr15:82959252-82959253	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs150910761	chr15:82959282-82959283	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs561851300	chr15:82959293-82959294	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs201697700	chr15:82959294-82959295	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs144066606	chr15:82959295-82959296	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs141281588	chr15:82959298-82959299	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs200825866	chr15:82959306-82959307	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs201801136	chr15:82959309-82959310	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs550329458	chr15:82959311-82959312	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs376765299	chr15:82959327-82959328	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs570323848	chr15:82959333-82959334	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs539303109	chr15:82959369-82959370	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs149530092	chr15:82959810-82959811	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs79430563	chr15:82959860-82959861	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs574840266	chr15:82959873-82959874	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs147200883	chr15:82959882-82959883	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs140495351	chr15:82959912-82959913	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs390120	chr15:82959925-82959926	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs557540909	chr15:82959938-82959939	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs533011017	chr15:82960035-82960036	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs147259331	chr15:82960062-82960063	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs185675949	chr15:82960069-82960070	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs546507312	chr15:82960097-82960098	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs373723283	chr15:82960138-82960139	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs113558179	chr15:82960220-82960221	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs145694562	chr15:82960228-82960229	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs560027135	chr15:82960248-82960249	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs572730867	chr15:82960282-82960283	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs377667630	chr15:82960319-82960320	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs142254601	chr15:82960355-82960356	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs369556149	chr15:82960356-82960357	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs373550697	chr15:82960360-82960361	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs561547513	chr15:82960377-82960378	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:76)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	CNVD
Wilms tumour	21544195	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
Melanoma	18172304	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
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Multiple myeloma	20724749	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Prostate cancer	18632612	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Cancer	16751803	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Autism	17322880	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Lung cancer	18438408	CNVD
Papillary thyroid carcinoma	22161024	CNVD
Autism	21480499	CNVD
Breast cancer	17603634	CNVD
Acute myeloid leukemia	16864856	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
small cell lung cancer	20016488	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Colorectal cancer	16774939	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Sudden cardiac death	19188705	CNVD
Breast cancer	21990379	CNVD
Myelofibrosis	22110671	CNVD
Congenital diaphragmatic hernia	21341218	CNVD
Adenocarcinoma	19607727	CNVD
Squamous cell cancer	19607727	CNVD
Congenital diaphragmatic hernia	20921022	CNVD
abnormal development	18461090	CNVD
Intellectual disability	22102821	CNVD
renal disease	17924346	CNVD
Breast cancer	20409316	CNVD
Mental retardation	17847001	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21785460	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21509527	CNVD
Williams Syndrome	20824207	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	21364760	CNVD
Ovarian cancer	21781307	CNVD
Epilepsy	20502679	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Renal cell carcinoma	21215367	CNVD

Chromatin state (count:802 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:82944200-82944600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
2	chr15:82944200-82945200	Active TSS	Fetal Intestine Large	intestine
3	chr15:82944200-82945400	Active TSS	H1 Cell Line	embryonic stem cell
4	chr15:82944200-82945800	Active TSS	iPS-20b Cell Line	embryonic stem cell
5	chr15:82944600-82945000	Active TSS	K562	blood
6	chr15:82944600-82945200	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr15:82944600-82945400	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
8	chr15:82944800-82945200	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr15:82944800-82945200	Active TSS	Primary T helper cells fromperipheralblood	blood
10	chr15:82944800-82945200	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
11	chr15:82944800-82945200	Active TSS	Fetal Stomach	stomach
12	chr15:82944800-82945200	Active TSS	HSMMtube	muscle
13	chr15:82944800-82945400	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
14	chr15:82944800-82945400	Active TSS	Cortex derived primary cultured neurospheres	brain
15	chr15:82944800-82945400	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
16	chr15:82944800-82945400	Active TSS	Fetal Brain Female	brain
17	chr15:82944800-82945400	Active TSS	Pancreatic Islets	Pancreatic Islet
18	chr15:82944800-82945400	Active TSS	Ovary	ovary
19	chr15:82944800-82945400	Active TSS	Pancreas	Pancrea
20	chr15:82944800-82945400	Active TSS	Right Atrium	heart
21	chr15:82944800-82945400	Active TSS	HSMM	muscle
22	chr15:82944800-82945800	Active TSS	HUES6 Cell Line	embryonic stem cell
23	chr15:82945000-82945400	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
24	chr15:82958200-82958400	Enhancers	iPS-18 Cell Line	embryonic stem cell
25	chr15:82959000-82959600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
26	chr15:82959800-82960200	Enhancers	Rectal Mucosa Donor 31	rectum
27	chr15:82959800-82960600	Enhancers	iPS-18 Cell Line	embryonic stem cell
28	chr15:82959800-82960600	Enhancers	Stomach Mucosa	stomach
29	chr15:82960200-82960600	Active TSS	Rectal Mucosa Donor 31	rectum
30	chr15:82960400-82960600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
31	chr15:82960400-82960800	Active TSS	Rectal Mucosa Donor 29	rectum
32	chr15:83002000-83002400	Active TSS	H9 Cell Line	embryonic stem cell
33	chr15:83002000-83002400	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
34	chr15:83002000-83002400	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
35	chr15:83002000-83002400	Active TSS	HUES64 Cell Line	embryonic stem cell
36	chr15:83002000-83002400	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
37	chr15:83002000-83002400	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
38	chr15:83002000-83002400	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
39	chr15:83002000-83002400	Active TSS	Breast Myoepithelial Primary Cells	Breast
40	chr15:83002000-83002400	Active TSS	Primary B cells from peripheral blood	blood
41	chr15:83002000-83002400	Active TSS	Primary T cells fromperipheralblood	blood
42	chr15:83002000-83002400	Active TSS	Primary T helper cells fromperipheralblood	blood
43	chr15:83002000-83002400	Active TSS	Primary T regulatory cells fromperipheralblood	blood
44	chr15:83002000-83002400	Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
45	chr15:83002000-83002400	Active TSS	Primary Natural Killer cells fromperipheralblood	blood
46	chr15:83002000-83002400	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
47	chr15:83002000-83002400	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
48	chr15:83002000-83002400	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
49	chr15:83002000-83002400	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
50	chr15:83002000-83002400	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin

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