Variant report

Variant	esv3449418
Chromosome Location	chr15:57024810-57026908
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:57025713-57025925	K562	blood:	n/a	chr15:57025866-57025881
2	ARID3A	chr15:57025353-57025517	HepG2	liver:	n/a	n/a
3	ATF3	chr15:57025727-57026071	K562	blood:	n/a	n/a
4	ATF3	chr15:57025587-57026149	A549	lung:	n/a	n/a
5	BACH1	chr15:57025790-57026076	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr15:57025819-57025887	K562	blood:	n/a	n/a
7	BCL3	chr15:57025652-57026449	A549	lung:	n/a	chr15:57026115-57026124
8	BCLAF1	chr15:57025458-57026101	K562	blood:	n/a	chr15:57025490-57025503 chr15:57025489-57025498 chr15:57025486-57025499 chr15:57025487-57025500
9	BCLAF1	chr15:57025094-57026060	GM12878	blood:	n/a	chr15:57025490-57025503 chr15:57025489-57025498 chr15:57025486-57025499 chr15:57025487-57025500 chr15:57025419-57025432
10	BCLAF1	chr15:57025231-57026076	GM12878	blood:	n/a	chr15:57025490-57025503 chr15:57025489-57025498 chr15:57025486-57025499 chr15:57025487-57025500 chr15:57025419-57025432
11	BHLHE40	chr15:57025004-57026278	K562	blood:	n/a	chr15:57025607-57025623 chr15:57025481-57025497
12	BHLHE40	chr15:57025189-57026058	HepG2	liver:	n/a	chr15:57025607-57025623 chr15:57025481-57025497
13	BHLHE40	chr15:57025704-57026024	A549	lung:	n/a	n/a
14	BHLHE40	chr15:57025178-57026089	GM12878	blood:	n/a	chr15:57025607-57025623 chr15:57025481-57025497
15	BRCA1	chr15:57025239-57025514	Hela-S3	cervix:	n/a	n/a
16	CBX3	chr15:57025646-57026279	K562	blood:	n/a	n/a
17	CBX3	chr15:57025036-57026468	HCT-116	colon:	n/a	n/a
18	CBX3	chr15:57024908-57026282	K562	blood:	n/a	n/a
19	CBX3	chr15:57025243-57026270	HCT-116	colon:	n/a	n/a
20	CCNT2	chr15:57025208-57026098	K562	blood:	n/a	n/a
21	CEBPB	chr15:57024965-57025874	Hela-S3	cervix:	n/a	n/a
22	CEBPD	chr15:57025179-57025949	HepG2	liver:	n/a	n/a
23	CHD1	chr15:57024493-57025864	GM12878	blood:	n/a	chr15:57025508-57025518 chr15:57025450-57025460
24	CHD1	chr15:57025194-57025578	H1-hESC	embryonic stem cell:	n/a	chr15:57025508-57025518 chr15:57025450-57025460
25	CHD2	chr15:57025344-57026061	H1-hESC	embryonic stem cell:	n/a	chr15:57025508-57025518 chr15:57025450-57025460
26	CHD2	chr15:57025676-57025941	HepG2	liver:	n/a	n/a
27	CHD2	chr15:57025206-57026047	Hela-S3	cervix:	n/a	chr15:57025508-57025518 chr15:57025450-57025460
28	CHD2	chr15:57025300-57025469	HepG2	liver:	n/a	chr15:57025450-57025460
29	CHD2	chr15:57025061-57026200	K562	blood:	n/a	chr15:57025508-57025518 chr15:57025450-57025460
30	CHD2	chr15:57025248-57026171	GM12878	blood:	n/a	chr15:57025508-57025518 chr15:57025450-57025460
31	CREB1	chr15:57025156-57026127	H1-hESC	embryonic stem cell:	n/a	n/a
32	CREB1	chr15:57025154-57026155	A549	lung:	n/a	n/a
33	CREB1	chr15:57025092-57026171	HepG2	liver:	n/a	n/a
34	CREB1	chr15:57025211-57026140	K562	blood:	n/a	n/a
35	CTCF	chr15:57025240-57025390	K562	blood:	n/a	n/a
36	CTCF	chr15:57025720-57025870	AG04449	skin:	n/a	n/a
37	CTCFL	chr15:57025803-57025975	K562	blood:	n/a	n/a
38	CUX1	chr15:57026361-57026419	K562	blood:	n/a	n/a
39	CUX1	chr15:57024417-57024915	K562	blood:	n/a	n/a
40	CUX1	chr15:57025783-57025876	K562	blood:	n/a	n/a
41	E2F4	chr15:57025286-57026157	K562	blood:	n/a	chr15:57025488-57025498 chr15:57025541-57025550 chr15:57025808-57025818 chr15:57025866-57025881
42	E2F4	chr15:57025316-57026027	MCF10A-Er-Src	breast:	n/a	chr15:57025488-57025498 chr15:57025541-57025550 chr15:57025808-57025818 chr15:57025866-57025881
43	E2F6	chr15:57024807-57026861	H1-hESC	embryonic stem cell:	n/a	chr15:57025488-57025498 chr15:57025541-57025550 chr15:57025808-57025818 chr15:57025866-57025881
44	E2F6	chr15:57025160-57026154	Hela-S3	cervix:	n/a	chr15:57025488-57025498 chr15:57025541-57025550 chr15:57025808-57025818 chr15:57025866-57025881
45	E2F6	chr15:57024999-57026450	H1-hESC	embryonic stem cell:	n/a	chr15:57025488-57025498 chr15:57025541-57025550 chr15:57025808-57025818 chr15:57025866-57025881
46	E2F6	chr15:57025107-57026170	K562	blood:	n/a	chr15:57025488-57025498 chr15:57025541-57025550 chr15:57025808-57025818 chr15:57025866-57025881
47	E2F6	chr15:57025193-57025673	K562	blood:	n/a	chr15:57025488-57025498 chr15:57025541-57025550
48	E2F6	chr15:57025077-57026368	K562	blood:	n/a	chr15:57025488-57025498 chr15:57025541-57025550 chr15:57025808-57025818 chr15:57025866-57025881
49	E2F6	chr15:57024968-57026543	A549	lung:	n/a	chr15:57025488-57025498 chr15:57025541-57025550 chr15:57025808-57025818 chr15:57025866-57025881
50	E2F6	chr15:57025702-57026150	K562	blood:	n/a	chr15:57025808-57025818 chr15:57025866-57025881

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:57025816-57025866	SK-N-MC	brain:	n/a
2	chr15:57026064-57026114	GM12878	blood:	n/a
3	chr15:57025818-57025868	NHDF-neo	bronchial:	n/a
4	chr15:57025816-57025866	SK-N-MC	brain:	n/a
5	chr15:57026064-57026114	GM12878	blood:	n/a
6	chr15:57025818-57025868	NHDF-neo	bronchial:	n/a
7	chr15:57025816-57025866	HCPEpiC	choroid plexus:	n/a
8	chr15:57026056-57026106	IMR90	lung:	fetal
9	chr15:57026056-57026106	Caco-2	colon:	n/a
10	chr15:57025234-57025284	NB4	blood:	n/a
11	chr15:57025234-57025284	AG09309	skin:	n/a
12	chr15:57025818-57025868	AG10803	skin:	n/a
13	chr15:57025234-57025284	SK-N-SH_RA	brain:	n/a
14	chr15:57026315-57026365	NHBE	bronchial:	n/a
15	chr15:57025528-57025578	AoSMC	blood vessel:	n/a
16	chr15:57025234-57025284	CMK	blood:	n/a
17	chr15:57026056-57026106	SK-N-SH	brain:	n/a
18	chr15:57026014-57026064	T-47D	breast:	n/a
19	chr15:57025234-57025284	LNCaP	prostate:	n/a
20	chr15:57026056-57026106	AG09319	gingival:	n/a
21	chr15:57025234-57025284	MCF10A-Er-Src	breast:	n/a
22	chr15:57025528-57025578	SKMC	muscle:	n/a
23	chr15:57025818-57025868	ECC-1	luminal epithelium:	n/a
24	chr15:57025818-57025868	HRE	kidney:	n/a
25	chr15:57025528-57025578	HIPEpiC	eye:	n/a
26	chr15:57025234-57025284	IMR90	lung:	fetal
27	chr15:57026014-57026064	HRCEpiC	kidney:	n/a
28	chr15:57026315-57026365	HRE	kidney:	n/a
29	chr15:57025528-57025578	HRE	kidney:	n/a
30	chr15:57026064-57026114	SKMC	muscle:	n/a
31	chr15:57025528-57025578	AG09309	skin:	n/a
32	chr15:57025818-57025868	HRPEpiC	eye:	n/a
33	chr15:57026056-57026106	AG04449	skin:	fetal
34	chr15:57026064-57026114	NT2-D1	testis:	n/a
35	chr15:57025816-57025866	HUVEC	blood vessel:	n/a
36	chr15:57026056-57026106	ECC-1	luminal epithelium:	n/a
37	chr15:57025234-57025284	GM12892	blood:	n/a
38	chr15:57025528-57025578	NHBE	bronchial:	n/a
39	chr15:57025234-57025284	H1-hESC	embryonic stem cell:	embryo
40	chr15:57025528-57025578	SK-N-SH	brain:	n/a
41	chr15:57025528-57025578	RPTEC	kidney:	n/a
42	chr15:57026315-57026365	HIPEpiC	eye:	n/a
43	chr15:57025818-57025868	T-47D	breast:	n/a
44	chr15:57026064-57026114	HRPEpiC	eye:	n/a
45	chr15:57026064-57026114	HRE	kidney:	n/a
46	chr15:57026064-57026114	HepG2	liver:	n/a
47	chr15:57026064-57026114	PFSK-1	brain:	n/a
48	chr15:57025816-57025866	SKMC	muscle:	n/a
49	chr15:57026014-57026064	HPAEpiC	pulmonary alveolar:	n/a
50	chr15:57025816-57025866	HEK293	kidney:	embryo

No.	Distal block	Cell Line	Cell type
1	chr15:56997588..56999927-chr15:57024317..57027282,2	K562	blood:
2	chr15:56989844..56991696-chr15:57023629..57025525,2	MCF-7	breast:
3	chr15:56534684..56537162-chr15:57025486..57027553,2	MCF-7	breast:
4	chr15:57023111..57027218-chr15:57209095..57213054,4	K562	blood:
5	chr15:57022824..57027100-chr15:57611258..57614634,3	K562	blood:
6	chr15:57006002..57008817-chr15:57023119..57025487,2	K562	blood:
7	chr15:57024542..57026335-chr15:57210196..57212175,2	K562	blood:
8	chr1:149223243..149225441-chr15:57024407..57026352,2	MCF-7	breast:
9	chr15:57023926..57025513-chr15:57178934..57180893,2	K562	blood:
10	chr15:56997588..57000196-chr15:57024112..57025817,2	K562	blood:
11	chr15:57025323..57025921-chr5:1801018..1801848,2	Hela-S3	cervix:
12	chr15:56999062..57001613-chr15:57024278..57025915,2	MCF-7	breast:
13	chr15:57023339..57026885-chr15:57210242..57212303,3	MCF-7	breast:
14	chr15:57022824..57025649-chr15:57612283..57614634,3	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MNS1-9	chr15:57024802-57025222	NONHSAT044030
2	lnc-MNS1-9	chr15:57025656-57025775	NONHSAT044030

Variant related genes	Relation type
ZNF280D	TF binding region
ZNF280D	CpG island
ENSG00000260172	chromatin interactions
ENSG00000181827	chromatin interactions
ENSG00000151575	chromatin interactions
ENSG00000140262	chromatin interactions
ENSG00000145494	chromatin interactions
ENSG00000206737	chromatin interactions
ENSG00000137871	chromatin interactions
ENSG00000171421	chromatin interactions

Extended variants
information (count: 90 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:90 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs561910928	chr15:57024836-57024837	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
2	rs6493884	chr15:57024930-57024931	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
3	rs569315915	chr15:57024955-57024956	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
4	rs532236975	chr15:57025009-57025010	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
5	rs552045544	chr15:57025010-57025011	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
6	rs565686617	chr15:57025078-57025079	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
7	rs534792680	chr15:57025094-57025095	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
8	rs554500399	chr15:57025095-57025096	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
9	rs567713844	chr15:57025102-57025103	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
10	rs566441930	chr15:57025118-57025119	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
11	rs536367331	chr15:57025133-57025134	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
12	rs556550813	chr15:57025161-57025162	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
13	rs576512365	chr15:57025179-57025180	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
14	rs545458242	chr15:57025208-57025209	Active TSS Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
15	rs559272317	chr15:57025249-57025250	Active TSS Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs572811699	chr15:57025255-57025256	Active TSS Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs12904421	chr15:57025258-57025259	Active TSS Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs561345627	chr15:57025281-57025282	Active TSS Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs200547154	chr15:57025285-57025286	Active TSS Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs529750489	chr15:57025307-57025308	Active TSS Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs190804442	chr15:57025308-57025309	Active TSS Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs563085700	chr15:57025330-57025331	Active TSS Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
23	rs531979721	chr15:57025376-57025377	Active TSS Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
24	rs550847878	chr15:57025378-57025379	Active TSS Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
25	rs551782129	chr15:57025441-57025442	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
26	rs561098225	chr15:57025459-57025460	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
27	rs565621326	chr15:57025485-57025486	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
28	rs528389070	chr15:57025513-57025514	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
29	rs548335149	chr15:57025517-57025518	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
30	rs568164491	chr15:57025538-57025539	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
31	rs372380256	chr15:57025553-57025554	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
32	rs575210787	chr15:57025641-57025642	Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
33	rs556683558	chr15:57025654-57025655	Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
34	rs377066659	chr15:57025704-57025705	Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	9 gene(s)	Overlapped CNVs	n/a
35	rs137950467	chr15:57025711-57025712	Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	9 gene(s)	Overlapped CNVs	n/a
36	rs143425903	chr15:57025733-57025734	Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	9 gene(s)	Overlapped CNVs	n/a
37	rs559008955	chr15:57025749-57025750	Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	9 gene(s)	Overlapped CNVs	n/a
38	rs112652493	chr15:57025756-57025757	Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	9 gene(s)	Overlapped CNVs	n/a
39	rs535011237	chr15:57025785-57025786	Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
40	rs555107409	chr15:57025793-57025794	Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
41	rs369808316	chr15:57025810-57025811	Active TSS Flanking Active TSS Bivalent/Poised TSS Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
42	rs544043832	chr15:57025853-57025854	Active TSS Flanking Active TSS Bivalent/Poised TSS Enhancers	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
43	rs563024899	chr15:57025937-57025938	Active TSS Flanking Active TSS Bivalent/Poised TSS Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
44	rs576561353	chr15:57025938-57025939	Active TSS Flanking Active TSS Bivalent/Poised TSS Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
45	rs116804950	chr15:57025957-57025958	Active TSS Flanking Active TSS Bivalent/Poised TSS Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
46	rs111873963	chr15:57025985-57025986	Active TSS Flanking Active TSS Bivalent/Poised TSS Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
47	rs558944335	chr15:57026005-57026006	ZNF genes & repeats Flanking Active TSS Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
48	rs373224807	chr15:57026010-57026011	ZNF genes & repeats Flanking Active TSS Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
49	rs7172313	chr15:57026028-57026029	ZNF genes & repeats Flanking Active TSS Active TSS Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
50	rs570869255	chr15:57026032-57026033	ZNF genes & repeats Flanking Active TSS Active TSS Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:58)

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
Gastric adenocarcinoma	19115996	CNVD
Congenital diaphragmatic hernia	21341218	CNVD
Holoprosencephaly	21359414	CNVD
Williams Syndrome	20824207	CNVD

Chromatin state (count:321 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:57012400-57025000	Weak transcription	Spleen	Spleen
2	chr15:57023400-57025200	Flanking Active TSS	Primary T cells from cord blood	blood
3	chr15:57023600-57025000	Weak transcription	Gastric	stomach
4	chr15:57023600-57025800	Active TSS	Thymus	Thymus
5	chr15:57023800-57025000	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
6	chr15:57023800-57025000	Flanking Active TSS	Fetal Brain Male	brain
7	chr15:57023800-57025200	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
8	chr15:57023800-57025200	Flanking Active TSS	Osteobl	bone
9	chr15:57023800-57025400	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
10	chr15:57023800-57025400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr15:57023800-57025400	Flanking Active TSS	HUVEC	blood vessel
12	chr15:57024000-57025000	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
13	chr15:57024000-57025000	Flanking Active TSS	Dnd41	blood
14	chr15:57024000-57025000	Flanking Active TSS	Hela-S3	cervix
15	chr15:57024000-57025000	Flanking Active TSS	NHEK	skin
16	chr15:57024000-57025200	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
17	chr15:57024000-57025400	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
18	chr15:57024000-57025400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
19	chr15:57024000-57025400	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
20	chr15:57024000-57025800	Active TSS	Right Ventricle	heart
21	chr15:57024200-57025000	Flanking Active TSS	Primary T helper memory cells from peripheral blood 2	blood
22	chr15:57024200-57025200	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
23	chr15:57024200-57025200	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
24	chr15:57024200-57025200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
25	chr15:57024200-57025400	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
26	chr15:57024200-57025400	Flanking Active TSS	Primary B cells from cord blood	blood
27	chr15:57024200-57025400	Flanking Active TSS	Adipose Nuclei	Adipose
28	chr15:57024200-57025400	Active TSS	Right Atrium	heart
29	chr15:57024200-57025800	Active TSS	Colonic Mucosa	Colon
30	chr15:57024200-57025800	Active TSS	Left Ventricle	heart
31	chr15:57024200-57026000	Active TSS	Fetal Muscle Trunk	muscle
32	chr15:57024200-57026000	Active TSS	Skeletal Muscle Male	skeletal muscle
33	chr15:57024200-57026200	Active TSS	Aorta	Aorta
34	chr15:57024200-57026200	Active TSS	Ovary	ovary
35	chr15:57024200-57026200	Active TSS	Psoas Muscle	Psoas
36	chr15:57024200-57026400	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
37	chr15:57024400-57025000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
38	chr15:57024400-57025000	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr15:57024400-57025000	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr15:57024400-57025000	Flanking Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
41	chr15:57024400-57025000	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
42	chr15:57024400-57025000	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
43	chr15:57024400-57025200	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
44	chr15:57024400-57025200	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
45	chr15:57024400-57025200	Flanking Active TSS	Primary B cells from peripheral blood	blood
46	chr15:57024400-57025200	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
47	chr15:57024400-57025200	Flanking Active TSS	Primary T killer memory cells from peripheral blood	blood
48	chr15:57024400-57025200	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
49	chr15:57024400-57025200	Transcr. at gene 5' and 3'	Duodenum Smooth Muscle	Duodenum
50	chr15:57024400-57025400	Active TSS	ES-WA7 Cell Line	embryonic stem cell

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