Variant report

Variant	nsv511550
Chromosome Location	chr15:44120559-44148142
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:75)
CpG islands
(count:61)
Chromatin interactive
region (count:23)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:75 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BATF	chr15:44120266-44120564	GM12878	blood:	n/a	n/a
2	CCNT2	chr15:44136197-44136385	K562	blood:	n/a	n/a
3	CEBPB	chr15:44146645-44147302	A549	lung:	n/a	n/a
4	CEBPB	chr15:44147028-44147251	K562	blood:	n/a	n/a
5	CEBPB	chr15:44147008-44147367	IMR90	lung:	n/a	n/a
6	CEBPB	chr15:44120595-44120751	HepG2	liver:	n/a	chr15:44120663-44120674
7	CEBPB	chr15:44146654-44147263	HepG2	liver:	n/a	n/a
8	CEBPB	chr15:44146591-44147274	K562	blood:	n/a	n/a
9	CEBPB	chr15:44127600-44127800	Hela-S3	cervix:	n/a	n/a
10	CEBPB	chr15:44147098-44147231	H1-hESC	embryonic stem cell:	n/a	n/a
11	CEBPB	chr15:44146585-44147402	Hela-S3	cervix:	n/a	n/a
12	CHD1	chr15:44124474-44124489	GM12878	blood:	n/a	n/a
13	CTCF	chr15:44139144-44139174	MCF-7	breast:	n/a	n/a
14	CTCF	chr15:44144498-44144586	MCF-7	breast:	n/a	n/a
15	CTCF	chr15:44126480-44126530	LNCaP	prostate:	n/a	n/a
16	CTCF	chr15:44144800-44144822	Kidney_OC	kidney:	n/a	n/a
17	CTCF	chr15:44144823-44144856	Kidney_OC	kidney:	n/a	n/a
18	CTCF	chr15:44127965-44128051	Pancreas_OC	pancreas:	n/a	n/a
19	E2F4	chr15:44125377-44125494	MCF10A-Er-Src	breast:	n/a	n/a
20	FOS	chr15:44147085-44147285	MCF10A-Er-Src	breast:	n/a	n/a
21	FOS	chr15:44147065-44147355	MCF10A-Er-Src	breast:	n/a	n/a
22	FOS	chr15:44147044-44147360	MCF10A-Er-Src	breast:	n/a	n/a
23	GTF3C2	chr15:44119440-44120568	Hela-S3	cervix:	n/a	n/a
24	IRF1	chr15:44120337-44120603	K562	blood:	n/a	chr15:44120589-44120603 chr15:44120591-44120602 chr15:44120593-44120603
25	IRF1	chr15:44120325-44120912	K562	blood:	n/a	chr15:44120591-44120605 chr15:44120589-44120603 chr15:44120591-44120602 chr15:44120593-44120603
26	JUND	chr15:44147154-44147509	HepG2	liver:	n/a	n/a
27	JUND	chr15:44128180-44128231	K562	blood:	n/a	n/a
28	MAFK	chr15:44128085-44128118	HepG2	liver:	n/a	n/a
29	MYC	chr15:44136434-44136503	MCF10A-Er-Src	breast:	n/a	n/a
30	MYC	chr15:44144550-44144566	MCF-7	breast:	n/a	n/a
31	NFE2	chr15:44120771-44120854	GM12878	blood:	n/a	n/a
32	NRF1	chr15:44120881-44120973	H1-hESC	embryonic stem cell:	n/a	n/a
33	NRF1	chr15:44147699-44147703	H1-hESC	embryonic stem cell:	n/a	n/a
34	PAX5	chr15:44123078-44123368	GM12878	blood:	n/a	n/a
35	PAX5	chr15:44123050-44123401	GM12878	blood:	n/a	n/a
36	PAX5	chr15:44122897-44123327	GM12878	blood:	n/a	n/a
37	POLR2A	chr15:44146443-44146798	Hela-S3	cervix:	n/a	n/a
38	POLR2A	chr15:44146341-44146674	K562	blood:	n/a	n/a
39	POLR2A	chr15:44124835-44124840	HepG2	liver:	n/a	n/a
40	POLR2A	chr15:44146912-44147175	K562	blood:	n/a	n/a
41	POLR2A	chr15:44144433-44144586	Gliobla	brain:	n/a	n/a
42	POLR2A	chr15:44140235-44140357	K562	blood:	n/a	n/a
43	POLR2A	chr15:44133651-44133799	Hela-S3	cervix:	n/a	n/a
44	POLR2A	chr15:44146574-44146716	H1-hESC	embryonic stem cell:	n/a	n/a
45	POLR2A	chr15:44146525-44146854	K562	blood:	n/a	n/a
46	POLR2A	chr15:44147213-44147395	K562	blood:	n/a	n/a
47	POLR2A	chr15:44143114-44143129	K562	blood:	n/a	n/a
48	POLR2A	chr15:44140993-44141065	K562	blood:	n/a	n/a
49	POLR2A	chr15:44120518-44120648	MCF10A-Er-Src	breast:	n/a	n/a
50	POLR2A	chr15:44146353-44146736	GM12892	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:44121440-44121490	NHBE	bronchial:	n/a
2	chr15:44121440-44121490	ovcar-3	ovarian:	n/a
3	chr15:44121440-44121490	AG04450	lung:	fetal
4	chr15:44121440-44121490	GM19239	blood:	n/a
5	chr15:44121440-44121490	ECC-1	luminal epithelium:	n/a
6	chr15:44121440-44121490	PFSK-1	brain:	n/a
7	chr15:44121440-44121490	H1-hESC	embryonic stem cell:	embryo
8	chr15:44121440-44121490	Hepatocyte	liver:	n/a
9	chr15:44121440-44121490	HCPEpiC	choroid plexus:	n/a
10	chr15:44121440-44121490	T-47D	breast:	n/a
11	chr15:44121440-44121490	MCF-7	breast:	n/a
12	chr15:44121440-44121490	SAEC	small airway:	n/a
13	chr15:44121440-44121490	HRPEpiC	eye:	n/a
14	chr15:44121440-44121490	ProgFib	skin:	n/a
15	chr15:44121440-44121490	HCF	heart:	n/a
16	chr15:44121440-44121490	MCF10A-Er-Src	breast:	n/a
17	chr15:44121440-44121490	AoSMC	blood vessel:	n/a
18	chr15:44121440-44121490	SKMC	muscle:	n/a
19	chr15:44121440-44121490	NHDF-neo	bronchial:	n/a
20	chr15:44121440-44121490	RPTEC	kidney:	n/a
21	chr15:44121440-44121490	CMK	blood:	n/a
22	chr15:44121440-44121490	HAEpiC	amniotic membrane:	n/a
23	chr15:44121440-44121490	AG04449	skin:	fetal
24	chr15:44121440-44121490	BJ	skin:	n/a
25	chr15:44121440-44121490	HMEC	breast:	n/a
26	chr15:44121440-44121490	NH-A	brain:	n/a
27	chr15:44121440-44121490	SK-N-SH	brain:	n/a
28	chr15:44121440-44121490	NB4	blood:	n/a
29	chr15:44121440-44121490	HRE	kidney:	n/a
30	chr15:44121440-44121490	AG09309	skin:	n/a
31	chr15:44121440-44121490	GM12892	blood:	n/a
32	chr15:44121440-44121490	SK-N-SH_RA	brain:	n/a
33	chr15:44121440-44121490	HPAEpiC	pulmonary alveolar:	n/a
34	chr15:44121440-44121490	HUVEC	blood vessel:	n/a
35	chr15:44121440-44121490	GM12878	blood:	n/a
36	chr15:44121440-44121490	NT2-D1	testis:	n/a
37	chr15:44121440-44121490	AG09319	gingival:	n/a
38	chr15:44121440-44121490	LNCaP	prostate:	n/a
39	chr15:44121440-44121490	Hela-S3	cervix:	n/a
40	chr15:44121440-44121490	K562	blood:	n/a
41	chr15:44121440-44121490	HCM	heart:	n/a
42	chr15:44121440-44121490	HL-60	blood:	n/a
43	chr15:44121440-44121490	U87	brain:	n/a
44	chr15:44121440-44121490	HRCEpiC	kidney:	n/a
45	chr15:44121440-44121490	A549	lung:	n/a
46	chr15:44121440-44121490	GM12891	blood:	n/a
47	chr15:44121440-44121490	AG10803	skin:	n/a
48	chr15:44121440-44121490	HEEpiC	esophagus:	n/a
49	chr15:44121440-44121490	IMR90	lung:	fetal
50	chr15:44121440-44121490	HEK293	kidney:	embryo

(count:23 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:44126368..44128829-chr15:44131384..44133343,2	MCF-7	breast:
2	chr15:44117584..44119221-chr15:44131996..44134256,2	MCF-7	breast:
3	15:43782117-43785993..15:44128499-44135043	GM12878	blood:
4	chr15:44117635..44119521-chr15:44128819..44130697,2	K562	blood:
5	chr15:44127360..44129810-chr15:44129920..44131455,2	K562	blood:
6	chr15:44130808..44133244-chr15:44134272..44137291,3	K562	blood:
7	15:43792489-43802874..15:44128499-44135043	GM12878	blood:
8	chr15:44127766..44129594-chr15:44132655..44134848,2	K562	blood:
9	chr15:44127360..44129810-chr15:44129920..44131455,2	K562	blood:
10	chr15:44112442..44117510-chr15:44119138..44122295,7	K562	blood:
11	chr15:44130808..44133244-chr15:44134272..44137291,3	K562	blood:
12	chr15:44104530..44106694-chr15:44134713..44136678,2	K562	blood:
13	15:44080886-44089111..15:44128499-44135043	GM12878	blood:
14	15:44092692-44100030..15:44128499-44135043	GM12878	blood:
15	chr15:44117206..44122379-chr15:44123536..44128804,6	K562	blood:
16	chr15:44089858..44095024-chr15:44113933..44120718,10	MCF-7	breast:
17	chr15:44069535..44071546-chr15:44121080..44123545,2	K562	blood:
18	chr15:44126368..44128829-chr15:44131384..44133343,2	MCF-7	breast:
19	chr15:44125863..44128518-chr15:44133380..44134911,2	K562	blood:
20	chr15:44116010..44118806-chr15:44119254..44122105,3	K562	blood:
21	chr15:44127766..44129594-chr15:44132655..44134848,2	K562	blood:
22	chr15:44082965..44094882-chr15:44108427..44121402,26	K562	blood:
23	chr15:44125863..44128518-chr15:44133380..44134911,2	K562	blood:

No data

Variant related genes	Relation type
WDR76	TF binding region
MFAP1	TF binding region
WDR76	CpG island
MFAP1	CpG island
ENSG00000128886	chromatin interactions
ENSG00000242028	chromatin interactions
ENSG00000140259	chromatin interactions
ENSG00000221792	chromatin interactions
ENSG00000067369	chromatin interactions
ENSG00000184716	chromatin interactions
ENSG00000140264	chromatin interactions
ENSG00000092470	chromatin interactions

Extended variants
information (count: 1142 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:1142 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs678084	chr15:44120559-44120560	Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs531484079	chr15:44120588-44120589	Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
3	rs548371473	chr15:44120652-44120653	Weak transcription Genic enhancers Transcr. at gene 5' and 3' Strong transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
4	rs376511867	chr15:44120659-44120660	Weak transcription Genic enhancers Transcr. at gene 5' and 3' Strong transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
5	rs567617582	chr15:44120785-44120786	Weak transcription Genic enhancers Transcr. at gene 5' and 3' Strong transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
6	rs149246635	chr15:44120833-44120834	Weak transcription Genic enhancers Transcr. at gene 5' and 3' Strong transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
7	rs546665127	chr15:44120857-44120858	Weak transcription Genic enhancers Transcr. at gene 5' and 3' Strong transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
8	rs185916253	chr15:44120865-44120866	Weak transcription Genic enhancers Transcr. at gene 5' and 3' Strong transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
9	rs7183809	chr15:44120868-44120869	Weak transcription Genic enhancers Transcr. at gene 5' and 3' Strong transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
10	rs28613896	chr15:44120885-44120886	Weak transcription Genic enhancers Transcr. at gene 5' and 3' Strong transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
11	rs552408685	chr15:44120888-44120889	Weak transcription Genic enhancers Transcr. at gene 5' and 3' Strong transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
12	rs144427956	chr15:44120906-44120907	Weak transcription Genic enhancers Transcr. at gene 5' and 3' Strong transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
13	rs555860150	chr15:44120921-44120922	Weak transcription Genic enhancers Transcr. at gene 5' and 3' Strong transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
14	rs538015163	chr15:44120944-44120945	Weak transcription Genic enhancers Transcr. at gene 5' and 3' Strong transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
15	rs191211395	chr15:44120975-44120976	Weak transcription Genic enhancers Transcr. at gene 5' and 3' Strong transcription Active TSS Enhancers Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
16	rs112639519	chr15:44121015-44121016	Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
17	rs533921369	chr15:44121029-44121030	Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
18	rs3759790	chr15:44121030-44121031	Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
19	rs75037661	chr15:44121033-44121034	Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
20	rs28565507	chr15:44121034-44121035	Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
21	rs11353535	chr15:44121104-44121105	Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
22	rs398043222	chr15:44121117-44121118	Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
23	rs62023678	chr15:44121119-44121120	Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
24	rs545816031	chr15:44121162-44121163	Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
25	rs145315437	chr15:44121208-44121209	Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Active TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
26	rs576417647	chr15:44121214-44121215	Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Active TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
27	rs541629609	chr15:44121248-44121249	Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Active TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
28	rs142376660	chr15:44121274-44121275	Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Active TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
29	rs561955069	chr15:44121344-44121345	Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Active TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
30	rs530129923	chr15:44121373-44121374	Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Active TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
31	rs547121301	chr15:44121382-44121383	Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Active TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
32	rs147213585	chr15:44121440-44121441	Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3' Active TSS Genic enhancers	CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs532334030	chr15:44121448-44121449	Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3' Active TSS Genic enhancers	CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs552169698	chr15:44121461-44121462	Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3' Active TSS Genic enhancers	CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs569179991	chr15:44121489-44121490	Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3' Active TSS Genic enhancers	CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs538558187	chr15:44121495-44121496	Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3' Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs140547981	chr15:44121565-44121566	Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3' Active TSS Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs2930531	chr15:44121570-44121571	Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3' Active TSS Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
39	rs181919171	chr15:44121612-44121613	Weak transcription Strong transcription Enhancers Genic enhancers Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs77403686	chr15:44121643-44121644	Weak transcription Strong transcription Enhancers Genic enhancers Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs187417795	chr15:44121651-44121652	Weak transcription Strong transcription Enhancers Genic enhancers Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs539403246	chr15:44121653-44121654	Weak transcription Strong transcription Enhancers Genic enhancers Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs78513325	chr15:44121665-44121666	Weak transcription Strong transcription Enhancers Genic enhancers Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs377468523	chr15:44121696-44121697	Weak transcription Strong transcription Enhancers Genic enhancers Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs34835269	chr15:44121722-44121723	Weak transcription Strong transcription Enhancers Genic enhancers Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs28531819	chr15:44121790-44121791	Weak transcription Strong transcription Enhancers Genic enhancers Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
47	rs542253791	chr15:44121797-44121798	Weak transcription Strong transcription Enhancers Genic enhancers Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs374244683	chr15:44121878-44121879	Weak transcription Strong transcription Enhancers Genic enhancers Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs561732070	chr15:44121911-44121912	Weak transcription Strong transcription Enhancers Genic enhancers Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs532519195	chr15:44121950-44121951	Weak transcription Strong transcription Enhancers Genic enhancers Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:62)

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
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	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
Renal cell carcinoma	18765545	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	16272173	CNVD
Hepatocellular carcinoma	16750200	CNVD
Abnormal phenotypes	18644119	CNVD
Cancer	16751803	CNVD
Mental retardation	17124404	CNVD

Chromatin state (count:771 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:44117400-44150200	Weak transcription	Sigmoid Colon	Sigmoid Colon
2	chr15:44118400-44120800	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
3	chr15:44118400-44120800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr15:44118400-44121000	Active TSS	Fetal Kidney	kidney
5	chr15:44118600-44120600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
6	chr15:44118600-44120600	Flanking Active TSS	Muscle Satellite Cultured Cells	--
7	chr15:44118600-44120600	Active TSS	Thymus	Thymus
8	chr15:44118600-44120600	Active TSS	HSMM	muscle
9	chr15:44118600-44120800	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
10	chr15:44118600-44121200	Active TSS	Brain Germinal Matrix	brain
11	chr15:44118800-44120600	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
12	chr15:44118800-44120600	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
13	chr15:44118800-44120800	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
14	chr15:44118800-44121000	Flanking Active TSS	HUVEC	blood vessel
15	chr15:44118800-44121400	Active TSS	GM12878-XiMat	blood
16	chr15:44119000-44120600	Active TSS	Rectal Smooth Muscle	rectum
17	chr15:44119200-44120600	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
18	chr15:44119200-44120600	Flanking Active TSS	Primary T cells from cord blood	blood
19	chr15:44119200-44120600	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
20	chr15:44119200-44120600	Flanking Active TSS	Osteobl	bone
21	chr15:44119200-44120800	Active TSS	NHDF-Ad	bronchial
22	chr15:44119400-44120600	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
23	chr15:44119400-44120600	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
24	chr15:44119400-44121000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
25	chr15:44119600-44120600	Enhancers	Primary monocytes fromperipheralblood	blood
26	chr15:44119600-44120600	Enhancers	Primary hematopoietic stem cells	blood
27	chr15:44119600-44120600	Enhancers	Colon Smooth Muscle	Colon
28	chr15:44119600-44120600	Enhancers	Fetal Brain Male	brain
29	chr15:44119600-44120600	Active TSS	Fetal Muscle Leg	muscle
30	chr15:44119600-44120600	Active TSS	Rectal Mucosa Donor 31	rectum
31	chr15:44119600-44121800	Weak transcription	Placenta	Placenta
32	chr15:44119600-44123000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
33	chr15:44119600-44127200	Weak transcription	Left Ventricle	heart
34	chr15:44119600-44127200	Weak transcription	Ovary	ovary
35	chr15:44119600-44127600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
36	chr15:44119600-44127600	Weak transcription	Gastric	stomach
37	chr15:44119600-44130600	Weak transcription	Brain Anterior Caudate	brain
38	chr15:44119600-44134400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
39	chr15:44119600-44135200	Weak transcription	Lung	lung
40	chr15:44119600-44142000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
41	chr15:44119600-44143200	Weak transcription	Aorta	Aorta
42	chr15:44119600-44143400	Weak transcription	H9 Cell Line	embryonic stem cell
43	chr15:44119600-44150600	Weak transcription	Esophagus	oesophagus
44	chr15:44119600-44151000	Weak transcription	Placenta Amnion	Placenta Amnion
45	chr15:44119600-44156400	Weak transcription	Pancreas	Pancrea
46	chr15:44119600-44166000	Weak transcription	Spleen	Spleen
47	chr15:44119600-44169400	Weak transcription	Fetal Intestine Large	intestine
48	chr15:44119600-44172800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
49	chr15:44119600-44181800	Weak transcription	Small Intestine	intestine
50	chr15:44119600-44183200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell

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