Variant report

Variant	nsv974563
Chromosome Location	chr15:42096771-42099742
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:156)
CpG islands
(count:61)
Chromatin interactive
region (count:7)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:156 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:42098884-42098958	HepG2	liver:	n/a	n/a
2	BACH1	chr15:42099009-42099028	H1-hESC	embryonic stem cell:	n/a	n/a
3	CTCF	chr15:42098887-42099010	GM12878	blood:	n/a	n/a
4	CTCF	chr15:42098945-42098977	GM10266	blood:	n/a	n/a
5	CTCF	chr15:42098880-42099030	RPTEC	kidney:	n/a	n/a
6	CTCF	chr15:42098860-42099010	HEK293	kidney:	n/a	n/a
7	CTCF	chr15:42098870-42099022	GM12892	blood:	n/a	n/a
8	CTCF	chr15:42099120-42099270	HEEpiC	esophagus:	n/a	n/a
9	CTCF	chr15:42098819-42099079	A549	lung:	n/a	n/a
10	CTCF	chr15:42098880-42099030	SAEC	small airway:	n/a	n/a
11	CTCF	chr15:42097700-42097850	GM12866	blood:	n/a	n/a
12	CTCF	chr15:42098686-42099205	MCF-7	breast:	n/a	n/a
13	CTCF	chr15:42098804-42099092	GM12878	blood:	n/a	n/a
14	CTCF	chr15:42098900-42099050	RPTEC	kidney:	n/a	n/a
15	CTCF	chr15:42098916-42098967	Fibrobl	skin:	n/a	n/a
16	CTCF	chr15:42098900-42099050	HEEpiC	esophagus:	n/a	n/a
17	CTCF	chr15:42098878-42099027	GM19239	blood:	n/a	n/a
18	CTCF	chr15:42098802-42099055	HepG2	liver:	n/a	n/a
19	CTCF	chr15:42098820-42098970	HVMF	connective:	n/a	n/a
20	CTCF	chr15:42098860-42099047	GM12891	blood:	n/a	n/a
21	CTCF	chr15:42098840-42098990	NHEK	skin:	n/a	n/a
22	CTCF	chr15:42098920-42099070	AG09319	gingival:	n/a	n/a
23	CTCF	chr15:42098863-42099066	H1-hESC	embryonic stem cell:	n/a	n/a
24	CTCF	chr15:42098820-42099077	MCF-7	breast:	n/a	n/a
25	CTCF	chr15:42098840-42098990	AG04449	skin:	n/a	n/a
26	CTCF	chr15:42098860-42099010	HepG2	liver:	n/a	n/a
27	CTCF	chr15:42098840-42098990	HBMEC	blood vessel:	n/a	n/a
28	CTCF	chr15:42098900-42099050	MCF-7	breast:	n/a	n/a
29	CTCF	chr15:42098880-42099030	NHEK	skin:	n/a	n/a
30	CTCF	chr15:42098840-42099062	MCF-7	breast:	n/a	n/a
31	CTCF	chr15:42098960-42099110	A549	lung:	n/a	n/a
32	CTCF	chr15:42098845-42099057	MCF-7	breast:	n/a	n/a
33	CTCF	chr15:42098860-42099010	HCT-116	colon:	n/a	n/a
34	CTCF	chr15:42098880-42099030	HAc	cerebellar:	n/a	n/a
35	CTCF	chr15:42098940-42099090	HCT-116	colon:	n/a	n/a
36	CTCF	chr15:42098851-42099028	Kidney_OC	kidney:	n/a	n/a
37	CTCF	chr15:42098782-42099079	H1-hESC	embryonic stem cell:	n/a	n/a
38	CTCF	chr15:42099140-42099290	BE2_C	brain:	n/a	n/a
39	CTCF	chr15:42099140-42099290	RPTEC	kidney:	n/a	n/a
40	CTCF	chr15:42098900-42099050	HUVEC	blood vessel:	n/a	n/a
41	CTCF	chr15:42098807-42099119	K562	blood:	n/a	n/a
42	CTCF	chr15:42098920-42099070	BE2_C	brain:	n/a	n/a
43	CTCF	chr15:42098900-42099050	AG04449	skin:	n/a	n/a
44	CTCF	chr15:42098900-42099050	HCPEpiC	choroid plexus:	n/a	n/a
45	CTCF	chr15:42098933-42099004	Medullo	brain:	n/a	n/a
46	CTCF	chr15:42098840-42098990	BE2_C	brain:	n/a	n/a
47	CTCF	chr15:42098800-42098950	GM12873	blood:	n/a	n/a
48	CTCF	chr15:42098920-42099070	HRPEpiC	eye:	n/a	n/a
49	CTCF	chr15:42098780-42098930	GM12872	blood:	n/a	n/a
50	CTCF	chr15:42098900-42099050	GM12871	blood:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:42097924-42097974	IMR90	lung:	fetal
2	chr15:42097924-42097974	PFSK-1	brain:	n/a
3	chr15:42097924-42097974	AoSMC	blood vessel:	n/a
4	chr15:42097924-42097974	HRPEpiC	eye:	n/a
5	chr15:42097924-42097974	CMK	blood:	n/a
6	chr15:42097924-42097974	MCF10A-Er-Src	breast:	n/a
7	chr15:42097924-42097974	HEK293	kidney:	embryo
8	chr15:42097924-42097974	H1-hESC	embryonic stem cell:	embryo
9	chr15:42097924-42097974	NHDF-neo	bronchial:	n/a
10	chr15:42097924-42097974	BE2_C	brain:	n/a
11	chr15:42097924-42097974	PrEC	prostate:	n/a
12	chr15:42097924-42097974	Caco-2	colon:	n/a
13	chr15:42097924-42097974	ovcar-3	ovarian:	n/a
14	chr15:42097924-42097974	HL-60	blood:	n/a
15	chr15:42097924-42097974	NHBE	bronchial:	n/a
16	chr15:42097924-42097974	HAEpiC	amniotic membrane:	n/a
17	chr15:42097924-42097974	HPAEpiC	pulmonary alveolar:	n/a
18	chr15:42097924-42097974	GM12878	blood:	n/a
19	chr15:42097924-42097974	Hepatocyte	liver:	n/a
20	chr15:42097924-42097974	GM12891	blood:	n/a
21	chr15:42097924-42097974	MCF-7	breast:	n/a
22	chr15:42097924-42097974	AG04450	lung:	fetal
23	chr15:42097924-42097974	AG09309	skin:	n/a
24	chr15:42097924-42097974	HIPEpiC	eye:	n/a
25	chr15:42097924-42097974	SK-N-SH_RA	brain:	n/a
26	chr15:42097924-42097974	BJ	skin:	n/a
27	chr15:42097924-42097974	HMEC	breast:	n/a
28	chr15:42097924-42097974	GM12892	blood:	n/a
29	chr15:42097924-42097974	HCPEpiC	choroid plexus:	n/a
30	chr15:42097924-42097974	SKMC	muscle:	n/a
31	chr15:42097924-42097974	ECC-1	luminal epithelium:	n/a
32	chr15:42097924-42097974	HepG2	liver:	n/a
33	chr15:42097924-42097974	HUVEC	blood vessel:	n/a
34	chr15:42097924-42097974	AG10803	skin:	n/a
35	chr15:42097924-42097974	Hela-S3	cervix:	n/a
36	chr15:42097924-42097974	HCM	heart:	n/a
37	chr15:42097924-42097974	ProgFib	skin:	n/a
38	chr15:42097924-42097974	LNCaP	prostate:	n/a
39	chr15:42097924-42097974	GM06990	blood:	n/a
40	chr15:42097924-42097974	NB4	blood:	n/a
41	chr15:42097924-42097974	NH-A	brain:	n/a
42	chr15:42097924-42097974	HNPCEpiC	eye:	n/a
43	chr15:42097924-42097974	NT2-D1	testis:	n/a
44	chr15:42097924-42097974	T-47D	breast:	n/a
45	chr15:42097924-42097974	SK-N-MC	brain:	n/a
46	chr15:42097924-42097974	AG09319	gingival:	n/a
47	chr15:42097924-42097974	A549	lung:	n/a
48	chr15:42097924-42097974	HCF	heart:	n/a
49	chr15:42097924-42097974	SAEC	small airway:	n/a
50	chr15:42097924-42097974	HEEpiC	esophagus:	n/a

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:42096535..42097035-chr6:57036895..57037403,2	HCT-116	colon:
2	chr15:42064494..42065972-chr15:42098576..42099124,3	MCF-7	breast:
3	chr15:42099310..42101245-chr15:42106600..42108424,2	MCF-7	breast:
4	chr15:42096733..42098481-chr15:42102481..42104605,2	K562	blood:
5	chr15:41804293..41806206-chr15:42097508..42099902,2	K562	blood:
6	chr15:42090667..42093233-chr15:42097205..42099737,2	K562	blood:
7	chr15:42065831..42068593-chr15:42098636..42100420,3	MCF-7	breast:

No data

Variant related genes	Relation type
MAPKBP1	TF binding region
MAPKBP1	CpG island
ENSG00000137802	chromatin interactions
ENSG00000112208	chromatin interactions
ENSG00000226803	chromatin interactions
ENSG00000260814	chromatin interactions
ENSG00000062524	chromatin interactions

Extended variants
information (count: 107 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:107 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs555792554	chr15:42096784-42096785	Enhancers Genic enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs572563210	chr15:42096793-42096794	Enhancers Genic enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs147235573	chr15:42096820-42096821	Enhancers Genic enhancers Weak transcription Flanking Active TSS Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs559778463	chr15:42096835-42096836	Enhancers Genic enhancers Weak transcription Flanking Active TSS Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs577708800	chr15:42096850-42096851	Enhancers Genic enhancers Weak transcription Flanking Active TSS Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs543558871	chr15:42096858-42096859	Enhancers Genic enhancers Weak transcription Flanking Active TSS Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs1209333	chr15:42096917-42096918	Enhancers Genic enhancers Weak transcription Flanking Active TSS Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs4924575	chr15:42096926-42096927	Enhancers Genic enhancers Weak transcription Flanking Active TSS Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
9	rs542072536	chr15:42096992-42096993	Enhancers Genic enhancers Weak transcription Flanking Active TSS Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs527488495	chr15:42097079-42097080	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs527611446	chr15:42097102-42097103	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs541212590	chr15:42097148-42097149	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs919142	chr15:42097172-42097173	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs376529785	chr15:42097202-42097203	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs190550599	chr15:42097217-42097218	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs549904262	chr15:42097291-42097292	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs183555771	chr15:42097312-42097313	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs528894608	chr15:42097385-42097386	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs549621905	chr15:42097402-42097403	Weak transcription Enhancers Genic enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs566229333	chr15:42097417-42097418	Weak transcription Enhancers Genic enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs535371250	chr15:42097471-42097472	Weak transcription Enhancers Genic enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs561904682	chr15:42097472-42097473	Weak transcription Enhancers Genic enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs571512234	chr15:42097477-42097478	Weak transcription Enhancers Genic enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs571056663	chr15:42097482-42097483	Weak transcription Enhancers Genic enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs537108438	chr15:42097541-42097542	Weak transcription Enhancers Genic enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs535520878	chr15:42097603-42097604	Weak transcription Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs557051865	chr15:42097606-42097607	Weak transcription Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs144877932	chr15:42097607-42097608	Weak transcription Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs542634240	chr15:42097645-42097646	Weak transcription Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs553366034	chr15:42097672-42097673	Weak transcription Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs369320546	chr15:42097702-42097703	Weak transcription Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs1197690	chr15:42097736-42097737	Weak transcription Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs541383395	chr15:42097740-42097741	Weak transcription Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs564225030	chr15:42097746-42097747	Weak transcription Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs533168724	chr15:42097754-42097755	Weak transcription Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs543505253	chr15:42097771-42097772	Weak transcription Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs563258038	chr15:42097789-42097790	Weak transcription Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs562619349	chr15:42097812-42097813	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs548695060	chr15:42097813-42097814	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs186404291	chr15:42097829-42097830	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs191818617	chr15:42097845-42097846	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs147547973	chr15:42097886-42097887	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs576691077	chr15:42097895-42097896	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs540134743	chr15:42097904-42097905	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs139353504	chr15:42097915-42097916	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs376029580	chr15:42097925-42097926	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs182856482	chr15:42098035-42098036	Weak transcription Genic enhancers Enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs112175218	chr15:42098042-42098043	Weak transcription Genic enhancers Enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs187502169	chr15:42098092-42098093	Weak transcription Genic enhancers Enhancers Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs571473987	chr15:42098125-42098126	Weak transcription Genic enhancers Enhancers Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:68)

Disease	PMID	Source
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
Angelman syndrome	16183798	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
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
Breast cancer	21785460	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	17053054	CNVD
Cancer	20164920	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Cancer	21129771	CNVD
Papillary thyroid carcinoma	22161024	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	21045282	CNVD
Breast cancer	22032731	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Multiple myeloma	16616336	CNVD
Renal cell carcinoma	18765545	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Myelofibrosis	22110671	CNVD
Maculopathy	20981449	CNVD
Gastric adenocarcinoma	19115996	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:260 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:42070200-42109800	Weak transcription	Fetal Brain Male	brain
2	chr15:42083600-42104600	Weak transcription	Liver	Liver
3	chr15:42083600-42109200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr15:42083800-42098600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
5	chr15:42083800-42098600	Weak transcription	Pancreas	Pancrea
6	chr15:42083800-42098600	Weak transcription	A549	lung
7	chr15:42083800-42103200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
8	chr15:42083800-42103400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
9	chr15:42083800-42104400	Weak transcription	Colonic Mucosa	Colon
10	chr15:42083800-42105000	Weak transcription	Rectal Mucosa Donor 31	rectum
11	chr15:42083800-42119400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
12	chr15:42084000-42098400	Weak transcription	HUES6 Cell Line	embryonic stem cell
13	chr15:42085200-42097400	Weak transcription	Psoas Muscle	Psoas
14	chr15:42088600-42103000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
15	chr15:42089400-42114800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
16	chr15:42089800-42096800	Weak transcription	Brain Cingulate Gyrus	brain
17	chr15:42090000-42097400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
18	chr15:42090000-42109800	Weak transcription	Small Intestine	intestine
19	chr15:42090600-42101600	Weak transcription	Primary neutrophils fromperipheralblood	blood
20	chr15:42091000-42096800	Genic enhancers	Breast Myoepithelial Primary Cells	Breast
21	chr15:42091400-42096800	Weak transcription	Right Atrium	heart
22	chr15:42091400-42105400	Weak transcription	HSMMtube	muscle
23	chr15:42091800-42101200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr15:42092000-42097000	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
25	chr15:42092000-42097600	Weak transcription	NHLF	lung
26	chr15:42092000-42101600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
27	chr15:42092200-42099400	Strong transcription	Fetal Intestine Small	intestine
28	chr15:42092200-42109400	Weak transcription	HepG2	liver
29	chr15:42092400-42097000	Weak transcription	Fetal Heart	heart
30	chr15:42092400-42097800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
31	chr15:42093200-42097000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
32	chr15:42093200-42101600	Weak transcription	Ovary	ovary
33	chr15:42093200-42104800	Weak transcription	Sigmoid Colon	Sigmoid Colon
34	chr15:42093400-42096800	Weak transcription	Thymus	Thymus
35	chr15:42093400-42104000	Weak transcription	Cortex derived primary cultured neurospheres	brain
36	chr15:42093600-42096800	Weak transcription	Primary T helper cells fromperipheralblood	blood
37	chr15:42093600-42097800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
38	chr15:42093600-42098600	Weak transcription	Left Ventricle	heart
39	chr15:42093600-42099200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
40	chr15:42093600-42100000	Enhancers	HMEC	breast
41	chr15:42093600-42101800	Weak transcription	Adipose Nuclei	Adipose
42	chr15:42093600-42103200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
43	chr15:42093600-42103400	Weak transcription	Skeletal Muscle Female	skeletal muscle
44	chr15:42093600-42104200	Weak transcription	Rectal Mucosa Donor 29	rectum
45	chr15:42093600-42104200	Weak transcription	Dnd41	blood
46	chr15:42093600-42105200	Weak transcription	Brain Germinal Matrix	brain
47	chr15:42093800-42101400	Weak transcription	HSMM	muscle
48	chr15:42093800-42103400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
49	chr15:42094200-42097000	Weak transcription	Fetal Muscle Leg	muscle
50	chr15:42094200-42098000	Weak transcription	Brain Hippocampus Middle	brain

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