Variant report

Variant	esv2761872
Chromosome Location	chr15:56211065-56426501
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2480)
CpG islands
(count:978)
Chromatin interactive
region (count:146)
LncRNA
region (count:12)
Mature miRNA
region (count: 0)
miRNA target
sites (count:9)

(count:2480 , 50 per page) page: 1 2 3 4 5 6 7 ... 50

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:56290869-56290907	K562	blood:	n/a	n/a
2	ARID3A	chr15:56285218-56285455	K562	blood:	n/a	n/a
3	ARID3A	chr15:56344799-56345413	K562	blood:	n/a	chr15:56345362-56345378 chr15:56345363-56345379
4	ARID3A	chr15:56332578-56333150	HepG2	liver:	n/a	n/a
5	ARID3A	chr15:56244680-56245174	HepG2	liver:	n/a	n/a
6	ARID3A	chr15:56247314-56247923	HepG2	liver:	n/a	n/a
7	ARID3A	chr15:56229334-56229534	K562	blood:	n/a	n/a
8	ARID3A	chr15:56267850-56267851	K562	blood:	n/a	n/a
9	ARID3A	chr15:56285729-56285953	HepG2	liver:	n/a	n/a
10	ARID3A	chr15:56332739-56333117	K562	blood:	n/a	n/a
11	ARID3A	chr15:56335964-56336039	HepG2	liver:	n/a	n/a
12	ARID3A	chr15:56286628-56286918	K562	blood:	n/a	n/a
13	ATF1	chr15:56331861-56332106	K562	blood:	n/a	n/a
14	ATF1	chr15:56301135-56301199	K562	blood:	n/a	n/a
15	ATF1	chr15:56330262-56330473	K562	blood:	n/a	n/a
16	ATF1	chr15:56334784-56334889	K562	blood:	n/a	n/a
17	ATF1	chr15:56332674-56333153	K562	blood:	n/a	n/a
18	ATF1	chr15:56311295-56311472	K562	blood:	n/a	n/a
19	ATF1	chr15:56252017-56252189	K562	blood:	n/a	n/a
20	ATF1	chr15:56334057-56334515	K562	blood:	n/a	n/a
21	ATF1	chr15:56295967-56296197	K562	blood:	n/a	n/a
22	ATF1	chr15:56331028-56331089	K562	blood:	n/a	n/a
23	ATF1	chr15:56344675-56345224	K562	blood:	n/a	n/a
24	ATF1	chr15:56286965-56287213	K562	blood:	n/a	n/a
25	ATF3	chr15:56332688-56333008	HepG2	liver:	n/a	n/a
26	ATF3	chr15:56332652-56333227	HCT-116	colon:	n/a	n/a
27	ATF3	chr15:56332580-56333175	A549	lung:	n/a	n/a
28	ATF3	chr15:56244819-56245017	HepG2	liver:	n/a	n/a
29	ATF3	chr15:56332633-56333036	K562	blood:	n/a	n/a
30	ATF3	chr15:56332737-56332952	K562	blood:	n/a	n/a
31	ATF3	chr15:56295943-56296234	K562	blood:	n/a	chr15:56296138-56296151
32	ATF3	chr15:56332545-56333126	HepG2	liver:	n/a	n/a
33	ATF3	chr15:56332556-56333228	HCT-116	colon:	n/a	n/a
34	BACH1	chr15:56285350-56286282	H1-hESC	embryonic stem cell:	n/a	n/a
35	BACH1	chr15:56344826-56345270	H1-hESC	embryonic stem cell:	n/a	n/a
36	BATF	chr15:56336045-56336269	GM12878	blood:	n/a	n/a
37	BDP1	chr15:56332391-56332686	Hela-S3	cervix:	n/a	n/a
38	BHLHE40	chr15:56331823-56332101	K562	blood:	n/a	n/a
39	BHLHE40	chr15:56285538-56285951	GM12878	blood:	n/a	n/a
40	BHLHE40	chr15:56332639-56332959	HepG2	liver:	n/a	chr15:56332856-56332865 chr15:56332856-56332865
41	BHLHE40	chr15:56291015-56291031	K562	blood:	n/a	n/a
42	BHLHE40	chr15:56332707-56332960	HepG2	liver:	n/a	chr15:56332856-56332865 chr15:56332856-56332865
43	BHLHE40	chr15:56335509-56335704	GM12878	blood:	n/a	n/a
44	BHLHE40	chr15:56332521-56333175	HepG2	liver:	n/a	chr15:56332856-56332865 chr15:56332856-56332865
45	BHLHE40	chr15:56244759-56245075	HepG2	liver:	n/a	n/a
46	BHLHE40	chr15:56398112-56398409	GM12878	blood:	n/a	n/a
47	BHLHE40	chr15:56332450-56333242	K562	blood:	n/a	chr15:56332856-56332865 chr15:56332856-56332865
48	BHLHE40	chr15:56285172-56286542	K562	blood:	n/a	chr15:56285460-56285476
49	BHLHE40	chr15:56344734-56345243	K562	blood:	n/a	n/a
50	BHLHE40	chr15:56298674-56298896	HepG2	liver:	n/a	n/a

(count:978 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:56286283-56286333	NT2-D1	testis:	n/a
2	chr15:56286067-56286117	BE2_C	brain:	n/a
3	chr15:56286283-56286333	NT2-D1	testis:	n/a
4	chr15:56286067-56286117	BE2_C	brain:	n/a
5	chr15:56285761-56285811	HPAEpiC	pulmonary alveolar:	n/a
6	chr15:56286067-56286117	AG04449	skin:	fetal
7	chr15:56285741-56285791	PrEC	prostate:	n/a
8	chr15:56286336-56286386	PANC-1	pancreas:	n/a
9	chr15:56284168-56284218	SK-N-SH_RA	brain:	n/a
10	chr15:56282277-56282327	HEEpiC	esophagus:	n/a
11	chr15:56286575-56286625	HCT-116	colon:	n/a
12	chr15:56286150-56286200	NHBE	bronchial:	n/a
13	chr15:56285261-56285311	AoSMC	blood vessel:	n/a
14	chr15:56285261-56285311	ovcar-3	ovarian:	n/a
15	chr15:56284168-56284218	K562	blood:	n/a
16	chr15:56286336-56286386	HEEpiC	esophagus:	n/a
17	chr15:56286067-56286117	LNCaP	prostate:	n/a
18	chr15:56290261-56290311	SK-N-MC	brain:	n/a
19	chr15:56286336-56286386	AG04450	lung:	fetal
20	chr15:56286336-56286386	GM12892	blood:	n/a
21	chr15:56284168-56284218	HRPEpiC	eye:	n/a
22	chr15:56286150-56286200	PANC-1	pancreas:	n/a
23	chr15:56290261-56290311	AG09309	skin:	n/a
24	chr15:56286067-56286117	HepG2	liver:	n/a
25	chr15:56282277-56282327	HepG2	liver:	n/a
26	chr15:56286150-56286200	HMEC	breast:	n/a
27	chr15:56401513-56401563	HNPCEpiC	eye:	n/a
28	chr15:56401513-56401563	HEEpiC	esophagus:	n/a
29	chr15:56401513-56401563	AG04450	lung:	fetal
30	chr15:56286067-56286117	PrEC	prostate:	n/a
31	chr15:56286283-56286333	GM12878	blood:	n/a
32	chr15:56342834-56342884	U87	brain:	n/a
33	chr15:56286150-56286200	Caco-2	colon:	n/a
34	chr15:56286283-56286333	GM06990	blood:	n/a
35	chr15:56286336-56286386	Caco-2	colon:	n/a
36	chr15:56401513-56401563	GM06990	blood:	n/a
37	chr15:56385430-56385480	HL-60	blood:	n/a
38	chr15:56282277-56282327	SK-N-SH_RA	brain:	n/a
39	chr15:56286283-56286333	MCF-7	breast:	n/a
40	chr15:56286150-56286200	HCF	heart:	n/a
41	chr15:56285261-56285311	Hela-S3	cervix:	n/a
42	chr15:56286067-56286117	Hepatocyte	liver:	n/a
43	chr15:56286067-56286117	BJ	skin:	n/a
44	chr15:56286336-56286386	SAEC	small airway:	n/a
45	chr15:56286575-56286625	GM12891	blood:	n/a
46	chr15:56285484-56285534	HL-60	blood:	n/a
47	chr15:56385430-56385480	MCF-7	breast:	n/a
48	chr15:56286150-56286200	HCT-116	colon:	n/a
49	chr15:56286336-56286386	AG09319	gingival:	n/a
50	chr15:56284168-56284218	AG04449	skin:	fetal

(count:146 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr15:56209638..56212268-chr15:56534926..56537157,2	MCF-7	breast:
2	chr11:110586878..110589672-chr15:56212609..56215497,2	MCF-7	breast:
3	chr15:56332693..56333405-chr15:56344692..56345448,2	MCF-7	breast:
4	chr15:56249710..56252114-chr15:56284678..56286584,2	MCF-7	breast:
5	chr15:56345036..56345575-chr15:56538156..56538672,2	MCF-7	breast:
6	chr15:56336255..56339253-chr15:56339399..56341903,2	K562	blood:
7	chr15:56332455..56334509-chr15:56340544..56343174,3	MCF-7	breast:
8	chr15:56285343..56287953-chr15:56307893..56310459,2	MCF-7	breast:
9	chr15:56379651..56381726-chr15:56393223..56394783,2	MCF-7	breast:
10	chr15:56375041..56376639-chr15:56378973..56381059,2	MCF-7	breast:
11	chr15:56308090..56310952-chr15:56323916..56326374,2	MCF-7	breast:
12	chr15:56331395..56333344-chr15:56535817..56538241,2	MCF-7	breast:
13	chr15:56369125..56370857-chr15:56537851..56540743,2	K562	blood:
14	chr15:56275489..56278398-chr15:56279462..56282619,4	K562	blood:
15	chr15:56389724..56392748-chr15:56393728..56397126,3	K562	blood:
16	chr15:56285499..56287418-chr15:56534884..56536553,2	K562	blood:
17	chr15:56281891..56284127-chr15:56288031..56290159,2	K562	blood:
18	chr15:56254403..56256035-chr15:56332964..56335048,2	MCF-7	breast:
19	chr15:56286056..56286943-chr15:56344508..56345311,2	MCF-7	breast:
20	chr15:56292596..56295463-chr15:56332389..56335036,2	MCF-7	breast:
21	chr15:56288413..56291274-chr15:56330655..56333525,2	MCF-7	breast:
22	chr15:56221865..56223584-chr15:56227077..56228974,2	MCF-7	breast:
23	chr15:56283238..56284535-chr15:56344426..56345460,6	MCF-7	breast:
24	chr15:56292596..56295463-chr15:56332389..56335036,2	MCF-7	breast:
25	chr15:56242510..56244333-chr15:56247480..56249699,2	MCF-7	breast:
26	chr15:56386726..56388923-chr15:56388990..56391326,2	MCF-7	breast:
27	chr15:56309924..56310815-chr15:56344688..56345628,4	MCF-7	breast:
28	chr15:56242510..56244333-chr15:56247480..56249699,2	MCF-7	breast:
29	chr15:56284455..56287261-chr15:56299264..56302045,2	MCF-7	breast:
30	chr15:56328944..56331210-chr15:56334121..56335862,3	MCF-7	breast:
31	chr15:56326019..56328776-chr15:56329119..56330730,3	MCF-7	breast:
32	chr15:56249277..56251562-chr15:56285197..56286697,2	MCF-7	breast:
33	chr15:56304158..56307081-chr15:56310322..56313297,2	K562	blood:
34	chr15:56344670..56345334-chr15:56537961..56538799,2	MCF-7	breast:
35	chr15:56251937..56254023-chr15:56256235..56258687,3	K562	blood:
36	chr15:56384379..56386985-chr15:56534620..56537262,4	MCF-7	breast:
37	chr15:56290352..56292488-chr15:56331467..56333363,2	MCF-7	breast:
38	chr15:56321602..56323899-chr15:56324883..56327290,2	K562	blood:
39	chr15:56275489..56279024-chr15:56279462..56282619,5	K562	blood:
40	chr15:56206449..56208647-chr15:56387606..56390052,2	MCF-7	breast:
41	chr15:56284173..56286171-chr15:56338265..56340590,2	MCF-7	breast:
42	chr15:56289959..56291765-chr15:56293575..56295875,2	K562	blood:
43	chr15:56259678..56262217-chr15:56262455..56264913,2	MCF-7	breast:
44	chr15:56379651..56381726-chr15:56393223..56394783,2	MCF-7	breast:
45	chr15:56404564..56406101-chr15:56409235..56411435,2	K562	blood:
46	chr15:56404564..56406101-chr15:56409235..56411435,2	K562	blood:
47	chr15:56389724..56392498-chr15:56393728..56396342,2	K562	blood:
48	chr15:56199193..56201528-chr15:56218643..56221076,2	MCF-7	breast:
49	chr15:56285739..56288392-chr15:56377133..56380147,3	MCF-7	breast:
50	chr15:56299007..56301700-chr15:56309609..56311858,2	MCF-7	breast:

(count:12 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NEDD4-1	chr15:56321886-56322179	NONHSAT044013
2	lnc-TEX9-2	chr15:56363619-56363837	NONHSAT044014
3	lnc-RFX7-2	chr15:56416129-56416163	l_1162_chr15:56293600-56416163_liver
4	lnc-RFX7-2	chr15:56293601-56293799	l_1162_chr15:56293600-56416163_liver
5	lnc-RFX7-2	chr15:56305102-56305262	l_1162_chr15:56293600-56416163_liver
6	lnc-RFX7-2	chr15:56321306-56321486	l_1162_chr15:56293600-56416163_liver
7	lnc-RFX7-3	chr15:56285709-56285811	NONHSAT044012
8	lnc-RFX7-3	chr15:56279929-56280199	NONHSAT044012
9	lnc-RFX7-2	chr15:56363458-56363839	l_1162_chr15:56293600-56416163_liver
10	lnc-RFX7-2	chr15:56325626-56325839	l_1162_chr15:56293600-56416163_liver
11	lnc-RFX7-2	chr15:56362416-56362488	l_1162_chr15:56293600-56416163_liver
12	lnc-RFX7-2	chr15:56359594-56359975	l_1162_chr15:56293600-56416163_liver

No data

(count:9 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	RFX7	hsa-miR-26b-5p	chr15:56384401-56384394
2	RFX7	hsa-miR-30b-5p	chr15:56383715-56383708
3	RFX7	hsa-miR-26b-5p	chr15:56384623-56384645
4	RFX7	hsa-miR-30b-5p	chr15:56383709-56383730
5	RFX7	hsa-miR-26b-5p	chr15:56384395-56384414
6	RFX7	hsa-miR-26b-5p	chr15:56383746-56383766
7	RFX7	hsa-miR-30b-5p	chr15:56383165-56383186
8	RFX7	hsa-miR-30b-5p	chr15:56383100-56383122
9	RFX7	hsa-miR-30b-5p	chr15:56383171-56383165

Variant related genes	Relation type
ENSG00000238513	TF binding region
CNOT6LP1	TF binding region
RN7SL568P	TF binding region
NEDD4	TF binding region
CD24P2	TF binding region
ENSG00000238513	CpG island
CNOT6LP1	CpG island
RN7SL568P	CpG island
NEDD4	CpG island
CD24P2	CpG island
ENSG00000162419	chromatin interactions
ENSG00000134186	chromatin interactions
ENSG00000253958	chromatin interactions
ENSG00000163191	chromatin interactions
ENSG00000156875	chromatin interactions
ENSG00000178974	chromatin interactions
ENSG00000135750	chromatin interactions
ENSG00000069869	chromatin interactions
ENSG00000151575	chromatin interactions
ENSG00000238513	chromatin interactions
ENSG00000233396	chromatin interactions
ENSG00000258413	chromatin interactions
ENSG00000196511	chromatin interactions
ENSG00000181827	chromatin interactions
ENSG00000239703	chromatin interactions
ENSG00000201558	chromatin interactions
ENSG00000185475	chromatin interactions
ENSG00000230183	chromatin interactions
ENSG00000176305	chromatin interactions

Extended variants
information (count: 8355 )
Associated
traits (count: 63 )

Variant overlapped rSNPs/rCNVs (count:8355 , 50 per page) page: 1 2 3 4 5 6 7 ... 168

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7172454	chr15:56211129-56211130	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs146793302	chr15:56211157-56211158	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs549625468	chr15:56211168-56211169	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs569554819	chr15:56211177-56211178	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs10518830	chr15:56211218-56211219	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs185381372	chr15:56211234-56211235	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs148514642	chr15:56211307-56211308	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs545491830	chr15:56211457-56211458	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs552986006	chr15:56211468-56211469	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs558205040	chr15:56211521-56211522	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs573433206	chr15:56211524-56211525	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs542399923	chr15:56211528-56211529	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs142861794	chr15:56211644-56211645	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs151074707	chr15:56211679-56211680	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs544978976	chr15:56211714-56211715	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs114708192	chr15:56211779-56211780	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs572874483	chr15:56211812-56211813	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs188240783	chr15:56211840-56211841	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs541976048	chr15:56211902-56211903	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs561900234	chr15:56211962-56211963	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs540677640	chr15:56211978-56211979	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs141043242	chr15:56212005-56212006	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs114566232	chr15:56212007-56212008	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs574655858	chr15:56212016-56212017	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs549564022	chr15:56212022-56212023	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs114051376	chr15:56212066-56212067	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs116638471	chr15:56212095-56212096	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs551793593	chr15:56212105-56212106	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs146777146	chr15:56212119-56212120	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs114148312	chr15:56212121-56212122	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs553388876	chr15:56212162-56212163	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs566990162	chr15:56212189-56212190	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs573300098	chr15:56212203-56212204	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs555895329	chr15:56212308-56212309	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs576167304	chr15:56212329-56212330	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs545229822	chr15:56212371-56212372	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs139794785	chr15:56212386-56212387	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs377613328	chr15:56212387-56212388	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs377080366	chr15:56212395-56212396	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs61628148	chr15:56212396-56212397	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs558570887	chr15:56212477-56212478	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs572332846	chr15:56212516-56212517	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs540614966	chr15:56212517-56212518	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs560494111	chr15:56212523-56212524	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs532306909	chr15:56212540-56212541	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs529376871	chr15:56212567-56212568	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs534477219	chr15:56212582-56212583	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs1912404	chr15:56212589-56212590	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
49	rs556134969	chr15:56212673-56212674	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs531801073	chr15:56212710-56212711	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:63)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	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
Melanoma	18172304	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
Intellectual disability	22102821	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	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
Chronic lymphocytic leukemia	21546498	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Basal cell lymphoma	17053054	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Cancer	21129771	CNVD
Breast cancer	16272173	CNVD
Hepatocellular carcinoma	16750200	CNVD
Abnormal phenotypes	18644119	CNVD
Cancer	16751803	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Acute monocytic leukemia	16498392	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Breast cancer	17133270	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Gastric adenocarcinoma	19115996	CNVD
Congenital diaphragmatic hernia	21341218	CNVD
Holoprosencephaly	21359414	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Pancreatic cancer	17952125	CNVD
Renal cell carcinoma	21215367	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:2840 , 50 per page) page: 1 2 3 4 5 6 7 ... 57

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:56176000-56216200	Weak transcription	Fetal Intestine Small	intestine
2	chr15:56188600-56218400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr15:56190000-56220000	Weak transcription	Pancreas	Pancrea
4	chr15:56190200-56221200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
5	chr15:56190400-56219800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
6	chr15:56200200-56213200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr15:56200800-56218000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
8	chr15:56201000-56230000	Weak transcription	Fetal Intestine Large	intestine
9	chr15:56201200-56217200	Weak transcription	Primary neutrophils fromperipheralblood	blood
10	chr15:56206800-56217800	Weak transcription	Duodenum Mucosa	Duodenum
11	chr15:56207600-56221200	Weak transcription	Right Ventricle	heart
12	chr15:56208600-56218000	Weak transcription	Esophagus	oesophagus
13	chr15:56208800-56221600	Weak transcription	Primary hematopoietic stem cells	blood
14	chr15:56208800-56230000	Weak transcription	Liver	Liver
15	chr15:56209000-56218400	Weak transcription	Fetal Stomach	stomach
16	chr15:56209000-56230400	Weak transcription	Primary T cells from cord blood	blood
17	chr15:56209200-56221200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
18	chr15:56209200-56221600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
19	chr15:56209200-56230200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
20	chr15:56209200-56230200	Weak transcription	Aorta	Aorta
21	chr15:56209400-56211800	Enhancers	Hela-S3	cervix
22	chr15:56209600-56216200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
23	chr15:56209600-56230800	Weak transcription	Stomach Smooth Muscle	stomach
24	chr15:56209600-56247400	Weak transcription	Psoas Muscle	Psoas
25	chr15:56210000-56216400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr15:56210200-56211600	Enhancers	A549	lung
27	chr15:56210200-56221600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
28	chr15:56210200-56229600	Weak transcription	HSMMtube	muscle
29	chr15:56210200-56229800	Weak transcription	Duodenum Smooth Muscle	Duodenum
30	chr15:56210600-56212600	Weak transcription	HMEC	breast
31	chr15:56210800-56212400	Weak transcription	NHDF-Ad	bronchial
32	chr15:56210800-56228800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
33	chr15:56210800-56229200	Weak transcription	HUVEC	blood vessel
34	chr15:56211000-56211400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
35	chr15:56211000-56212600	Weak transcription	Muscle Satellite Cultured Cells	--
36	chr15:56211000-56219800	Weak transcription	NHLF	lung
37	chr15:56211000-56221200	Weak transcription	NHEK	skin
38	chr15:56211000-56221800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
39	chr15:56211400-56230800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
40	chr15:56211600-56229400	Weak transcription	A549	lung
41	chr15:56211800-56242400	Weak transcription	Hela-S3	cervix
42	chr15:56212200-56218600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
43	chr15:56215000-56221200	Weak transcription	Thymus	Thymus
44	chr15:56215200-56216600	Weak transcription	Muscle Satellite Cultured Cells	--
45	chr15:56215200-56217600	Weak transcription	Spleen	Spleen
46	chr15:56216200-56217200	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
47	chr15:56216200-56217200	Strong transcription	Fetal Intestine Small	intestine
48	chr15:56216400-56216800	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
49	chr15:56216800-56230000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
50	chr15:56217200-56218400	Weak transcription	Fetal Intestine Small	intestine

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