Variant report

Variant	nsv9243
Chromosome Location	chr15:42101625-42103990
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:352)
CpG islands
(count:61)
Chromatin interactive
region (count:13)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:352 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:42103689-42103944	HepG2	liver:	n/a	n/a
2	BACH1	chr15:42103600-42103904	K562	blood:	n/a	n/a
3	BHLHE40	chr15:42103567-42103935	GM12878	blood:	n/a	n/a
4	BHLHE40	chr15:42103579-42103945	K562	blood:	n/a	n/a
5	CEBPB	chr15:42103728-42103816	H1-hESC	embryonic stem cell:	n/a	n/a
6	CEBPB	chr15:42103638-42103935	Hela-S3	cervix:	n/a	n/a
7	CHD1	chr15:42103358-42104102	IMR90	lung:	n/a	n/a
8	CHD1	chr15:42103729-42103906	GM12878	blood:	n/a	n/a
9	CHD2	chr15:42103810-42103812	K562	blood:	n/a	n/a
10	CHD2	chr15:42103336-42103347	GM12878	blood:	n/a	n/a
11	CHD2	chr15:42103693-42103927	GM12878	blood:	n/a	n/a
12	CHD2	chr15:42103726-42103884	H1-hESC	embryonic stem cell:	n/a	n/a
13	CHD2	chr15:42103721-42103943	HepG2	liver:	n/a	n/a
14	CREB1	chr15:42103685-42103880	A549	lung:	n/a	n/a
15	CTCF	chr15:42102880-42103030	AG09319	gingival:	n/a	n/a
16	CTCF	chr15:42103720-42103870	GM12865	blood:	n/a	n/a
17	CTCF	chr15:42103700-42103850	AG04449	skin:	n/a	n/a
18	CTCF	chr15:42102920-42103070	NHDF-neo	bronchial:	n/a	n/a
19	CTCF	chr15:42103720-42103870	AG04449	skin:	n/a	n/a
20	CTCF	chr15:42103595-42104092	K562	blood:	n/a	n/a
21	CTCF	chr15:42103655-42103929	MCF-7	breast:	n/a	n/a
22	CTCF	chr15:42102982-42103143	GM19239	blood:	n/a	n/a
23	CTCF	chr15:42103700-42103850	HRPEpiC	eye:	n/a	n/a
24	CTCF	chr15:42103740-42103890	HAc	cerebellar:	n/a	n/a
25	CTCF	chr15:42103666-42103923	Fibrobl	skin:	n/a	n/a
26	CTCF	chr15:42103590-42103965	SK-N-SH_RA	brain:	n/a	n/a
27	CTCF	chr15:42103680-42103830	GM12864	blood:	n/a	n/a
28	CTCF	chr15:42103678-42103899	H1-hESC	embryonic stem cell:	n/a	n/a
29	CTCF	chr15:42103700-42103850	HEK293	kidney:	n/a	n/a
30	CTCF	chr15:42103663-42103891	SK-N-SH_RA	brain:	n/a	n/a
31	CTCF	chr15:42102900-42103050	HA-sp	spinal cord:	n/a	n/a
32	CTCF	chr15:42103740-42103890	HRE	kidney:	n/a	n/a
33	CTCF	chr15:42103720-42103870	HPF	lung:	n/a	n/a
34	CTCF	chr15:42103658-42103935	A549	lung:	n/a	n/a
35	CTCF	chr15:42103700-42103850	GM12873	blood:	n/a	n/a
36	CTCF	chr15:42103548-42104066	K562	blood:	n/a	n/a
37	CTCF	chr15:42103600-42103750	HAc	cerebellar:	n/a	n/a
38	CTCF	chr15:42102980-42103130	HBMEC	blood vessel:	n/a	n/a
39	CTCF	chr15:42102932-42103133	GM19240	blood:	n/a	n/a
40	CTCF	chr15:42103657-42103841	ECC-1	luminal epithelium:	n/a	n/a
41	CTCF	chr15:42103700-42103850	HUVEC	blood vessel:	n/a	n/a
42	CTCF	chr15:42103610-42103967	Spleen_OC	spleen:	n/a	n/a
43	CTCF	chr15:42103598-42104035	MCF-7	breast:	n/a	n/a
44	CTCF	chr15:42103597-42103912	HepG2	liver:	n/a	n/a
45	CTCF	chr15:42103040-42103190	GM12871	blood:	n/a	n/a
46	CTCF	chr15:42103551-42103938	H1-hESC	embryonic stem cell:	n/a	n/a
47	CTCF	chr15:42102928-42103128	GM12892	blood:	n/a	n/a
48	CTCF	chr15:42103680-42103830	AG04450	lung:	n/a	n/a
49	CTCF	chr15:42103625-42103973	H1-hESC	embryonic stem cell:	n/a	n/a
50	CTCF	chr15:42103596-42103958	K562	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:42102381-42102431	HIPEpiC	eye:	n/a
2	chr15:42102381-42102431	RPTEC	kidney:	n/a
3	chr15:42102381-42102431	K562	blood:	n/a
4	chr15:42102381-42102431	HRE	kidney:	n/a
5	chr15:42102381-42102431	BE2_C	brain:	n/a
6	chr15:42102381-42102431	SK-N-SH_RA	brain:	n/a
7	chr15:42102381-42102431	AG04450	lung:	fetal
8	chr15:42102381-42102431	HRCEpiC	kidney:	n/a
9	chr15:42102381-42102431	GM06990	blood:	n/a
10	chr15:42102381-42102431	NHDF-neo	bronchial:	n/a
11	chr15:42102381-42102431	NH-A	brain:	n/a
12	chr15:42102381-42102431	HMEC	breast:	n/a
13	chr15:42102381-42102431	AG09319	gingival:	n/a
14	chr15:42102381-42102431	CMK	blood:	n/a
15	chr15:42102381-42102431	T-47D	breast:	n/a
16	chr15:42102381-42102431	MCF10A-Er-Src	breast:	n/a
17	chr15:42102381-42102431	HNPCEpiC	eye:	n/a
18	chr15:42102381-42102431	HUVEC	blood vessel:	n/a
19	chr15:42102381-42102431	AG09309	skin:	n/a
20	chr15:42102381-42102431	H1-hESC	embryonic stem cell:	embryo
21	chr15:42102381-42102431	SAEC	small airway:	n/a
22	chr15:42102381-42102431	HEEpiC	esophagus:	n/a
23	chr15:42102381-42102431	NT2-D1	testis:	n/a
24	chr15:42102381-42102431	AG10803	skin:	n/a
25	chr15:42102381-42102431	BJ	skin:	n/a
26	chr15:42102381-42102431	HL-60	blood:	n/a
27	chr15:42102381-42102431	LNCaP	prostate:	n/a
28	chr15:42102381-42102431	Caco-2	colon:	n/a
29	chr15:42102381-42102431	HCF	heart:	n/a
30	chr15:42102381-42102431	Jurkat	blood:	n/a
31	chr15:42102381-42102431	GM12891	blood:	n/a
32	chr15:42102381-42102431	GM12892	blood:	n/a
33	chr15:42102381-42102431	SK-N-MC	brain:	n/a
34	chr15:42102381-42102431	SKMC	muscle:	n/a
35	chr15:42102381-42102431	Hela-S3	cervix:	n/a
36	chr15:42102381-42102431	HPAEpiC	pulmonary alveolar:	n/a
37	chr15:42102381-42102431	GM19239	blood:	n/a
38	chr15:42102381-42102431	U87	brain:	n/a
39	chr15:42102381-42102431	ProgFib	skin:	n/a
40	chr15:42102381-42102431	MCF-7	breast:	n/a
41	chr15:42102381-42102431	HCPEpiC	choroid plexus:	n/a
42	chr15:42102381-42102431	PANC-1	pancreas:	n/a
43	chr15:42102381-42102431	SK-N-SH	brain:	n/a
44	chr15:42102381-42102431	HCM	heart:	n/a
45	chr15:42102381-42102431	HepG2	liver:	n/a
46	chr15:42102381-42102431	IMR90	lung:	fetal
47	chr15:42102381-42102431	HAEpiC	amniotic membrane:	n/a
48	chr15:42102381-42102431	PFSK-1	brain:	n/a
49	chr15:42102381-42102431	ECC-1	luminal epithelium:	n/a
50	chr15:42102381-42102431	HEK293	kidney:	embryo

(count:13 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:41988022..41988696-chr15:42103354..42104252,2	K562	blood:
2	chr15:42102419..42105107-chr15:42118936..42121739,2	MCF-7	breast:
3	chr15:42064231..42067337-chr15:42102963..42104752,21	K562	blood:
4	chr15:42064035..42067811-chr15:42102222..42105290,4	K562	blood:
5	chr15:42064299..42065172-chr15:42102196..42103016,2	MCF-7	breast:
6	chr15:42063995..42065627-chr15:42103084..42104266,14	MCF-7	breast:
7	chr15:42064618..42065570-chr15:42103319..42104238,3	MCF-7	breast:
8	chr15:41895763..41896358-chr15:42103332..42103836,2	MCF-7	breast:
9	chr15:42066441..42067175-chr15:42103083..42104316,4	MCF-7	breast:
10	chr15:42066384..42066972-chr15:42103408..42104272,2	MCF-7	breast:
11	chr15:41757721..41758661-chr15:42103319..42104236,5	K562	blood:
12	chr15:41849511..41850438-chr15:42103338..42104256,4	K562	blood:
13	chr15:42063685..42066999-chr15:42102378..42105267,3	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-JMJD7-PLA2G4B-6	chr15:42103376-42103524	NONHSAT041963
2	lnc-JMJD7-PLA2G4B-6	chr15:42102959-42103143	NONHSAT041963
3	lnc-JMJD7-PLA2G4B-7	chr15:42101244-42102741	NONHSAT041962

No data

Variant related genes	Relation type
MAPKBP1	TF binding region
MAPKBP1	CpG island
ENSG00000168970	chromatin interactions
ENSG00000260814	chromatin interactions
ENSG00000250379	chromatin interactions
ENSG00000137802	chromatin interactions
ENSG00000243789	chromatin interactions
ENSG00000092445	chromatin interactions

Extended variants
information (count: 91 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:91 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs189228423	chr15:42101631-42101632	Enhancers Weak transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
2	rs546403285	chr15:42101663-42101664	Enhancers Weak transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
3	rs16972089	chr15:42101694-42101695	Enhancers Weak transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Active TSS	TF binding region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
4	rs576479094	chr15:42101700-42101701	Enhancers Weak transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
5	rs549347247	chr15:42101702-42101703	Enhancers Weak transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
6	rs561606974	chr15:42101741-42101742	Enhancers Weak transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
7	rs543081443	chr15:42101761-42101762	Enhancers Weak transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
8	rs541960772	chr15:42101789-42101790	Enhancers Weak transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
9	rs181623483	chr15:42101806-42101807	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
10	rs527699639	chr15:42101959-42101960	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
11	rs546461628	chr15:42101985-42101986	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
12	rs559990244	chr15:42102079-42102080	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	lncRNA	n/a	Overlapped CNVs	n/a
13	rs117047949	chr15:42102223-42102224	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
14	rs551941426	chr15:42102266-42102267	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
15	rs12440605	chr15:42102285-42102286	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
16	rs537907294	chr15:42102288-42102289	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
17	rs549795857	chr15:42102300-42102301	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
18	rs147273269	chr15:42102305-42102306	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
19	rs533751567	chr15:42102346-42102347	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
20	rs555998048	chr15:42102348-42102349	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
21	rs553838045	chr15:42102413-42102414	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
22	rs544424413	chr15:42102445-42102446	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
23	rs72724172	chr15:42102479-42102480	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
24	rs556740210	chr15:42102565-42102566	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
25	rs540182847	chr15:42102568-42102569	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
26	rs11631051	chr15:42102579-42102580	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
27	rs186541201	chr15:42102604-42102605	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
28	rs532215582	chr15:42102646-42102647	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
29	rs192377216	chr15:42102649-42102650	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
30	rs35072367	chr15:42102661-42102662	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
31	rs34606302	chr15:42102711-42102712	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
32	rs572232629	chr15:42102721-42102722	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
33	rs565669597	chr15:42102731-42102732	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
34	rs12148611	chr15:42102738-42102739	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
35	rs559571646	chr15:42102740-42102741	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
36	rs145409806	chr15:42102741-42102742	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
37	rs11415317	chr15:42102742-42102743	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
38	rs67741572	chr15:42102760-42102761	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
39	rs541009755	chr15:42102776-42102777	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
40	rs564178260	chr15:42102808-42102809	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
41	rs12441300	chr15:42102845-42102846	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
42	rs74773620	chr15:42102913-42102914	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
43	rs570812262	chr15:42102916-42102917	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
44	rs77757924	chr15:42102919-42102920	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
45	rs552064102	chr15:42102933-42102934	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
46	rs373906662	chr15:42102935-42102936	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
47	rs368497745	chr15:42102936-42102937	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
48	rs372441864	chr15:42102937-42102938	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
49	rs375940034	chr15:42102938-42102939	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
50	rs562671603	chr15:42102954-42102955	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	6 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:244 , 50 per page) page: 1 2 3 4 5

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	chr15:42083800-42103200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
5	chr15:42083800-42103400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
6	chr15:42083800-42104400	Weak transcription	Colonic Mucosa	Colon
7	chr15:42083800-42105000	Weak transcription	Rectal Mucosa Donor 31	rectum
8	chr15:42083800-42119400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
9	chr15:42088600-42103000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
10	chr15:42089400-42114800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
11	chr15:42090000-42109800	Weak transcription	Small Intestine	intestine
12	chr15:42091400-42105400	Weak transcription	HSMMtube	muscle
13	chr15:42092200-42109400	Weak transcription	HepG2	liver
14	chr15:42093200-42104800	Weak transcription	Sigmoid Colon	Sigmoid Colon
15	chr15:42093400-42104000	Weak transcription	Cortex derived primary cultured neurospheres	brain
16	chr15:42093600-42101800	Weak transcription	Adipose Nuclei	Adipose
17	chr15:42093600-42103200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
18	chr15:42093600-42103400	Weak transcription	Skeletal Muscle Female	skeletal muscle
19	chr15:42093600-42104200	Weak transcription	Rectal Mucosa Donor 29	rectum
20	chr15:42093600-42104200	Weak transcription	Dnd41	blood
21	chr15:42093600-42105200	Weak transcription	Brain Germinal Matrix	brain
22	chr15:42093800-42103400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
23	chr15:42094200-42102000	Weak transcription	Primary B cells from cord blood	blood
24	chr15:42094200-42104400	Weak transcription	Fetal Lung	lung
25	chr15:42094200-42104600	Weak transcription	Monocytes-CD14+_RO01746	blood
26	chr15:42094600-42104400	Weak transcription	Fetal Brain Female	brain
27	chr15:42094800-42103200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
28	chr15:42095200-42104400	Weak transcription	GM12878-XiMat	blood
29	chr15:42097000-42101800	Weak transcription	Primary T cells fromperipheralblood	blood
30	chr15:42097000-42103400	Weak transcription	Skeletal Muscle Male	skeletal muscle
31	chr15:42097000-42104200	Weak transcription	Aorta	Aorta
32	chr15:42097000-42104800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
33	chr15:42097200-42111000	Weak transcription	Fetal Kidney	kidney
34	chr15:42097400-42103000	Weak transcription	Primary T helper cells fromperipheralblood	blood
35	chr15:42097400-42103400	Weak transcription	Primary T helper cells PMA-I stimulated	--
36	chr15:42097600-42101800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
37	chr15:42097600-42103400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
38	chr15:42097600-42103600	Genic enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
39	chr15:42097600-42104200	Weak transcription	Thymus	Thymus
40	chr15:42097600-42104400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
41	chr15:42097600-42107800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr15:42097800-42119600	Weak transcription	Psoas Muscle	Psoas
43	chr15:42098000-42103000	Weak transcription	Brain Substantia Nigra	brain
44	chr15:42098000-42103200	Weak transcription	Brain Anterior Caudate	brain
45	chr15:42098000-42103800	Weak transcription	Fetal Muscle Leg	muscle
46	chr15:42098200-42104200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
47	chr15:42098200-42118800	Strong transcription	Fetal Stomach	stomach
48	chr15:42098600-42103600	Genic enhancers	NHEK	skin
49	chr15:42098800-42115600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
50	chr15:42099000-42101800	Weak transcription	Brain Hippocampus Middle	brain

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