Variant report

Variant	esv3438792
Chromosome Location	chr15:73343424-73346772
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:589)
CpG islands
(count:672)
Chromatin interactive
region (count:4)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:589 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:73345383-73345909	HepG2	liver:	n/a	n/a
2	ARID3A	chr15:73345400-73345630	K562	blood:	n/a	n/a
3	ARID3A	chr15:73344291-73344503	HepG2	liver:	n/a	n/a
4	ATF2	chr15:73345276-73345639	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr15:73343891-73344645	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr15:73345235-73345796	H1-hESC	embryonic stem cell:	n/a	n/a
7	BHLHE40	chr15:73344180-73344578	GM12878	blood:	n/a	chr15:73344535-73344551
8	BRCA1	chr15:73345429-73345814	H1-hESC	embryonic stem cell:	n/a	n/a
9	BRCA1	chr15:73345427-73345617	Hela-S3	cervix:	n/a	n/a
10	CCNT2	chr15:73344871-73345124	K562	blood:	n/a	n/a
11	CCNT2	chr15:73344372-73344618	K562	blood:	n/a	chr15:73344508-73344517
12	CEBPB	chr15:73345359-73345646	Hela-S3	cervix:	n/a	n/a
13	CEBPD	chr15:73344779-73344987	HepG2	liver:	n/a	n/a
14	CEBPD	chr15:73344119-73344603	HepG2	liver:	n/a	n/a
15	CHD1	chr15:73345494-73346262	H1-hESC	embryonic stem cell:	n/a	chr15:73345643-73345653
16	CHD1	chr15:73344948-73345082	H1-hESC	embryonic stem cell:	n/a	n/a
17	CHD2	chr15:73344416-73344558	H1-hESC	embryonic stem cell:	n/a	n/a
18	CHD2	chr15:73345353-73345824	H1-hESC	embryonic stem cell:	n/a	chr15:73345643-73345653
19	CHD2	chr15:73344411-73344507	K562	blood:	n/a	n/a
20	CHD2	chr15:73345576-73345678	K562	blood:	n/a	chr15:73345643-73345653
21	CHD2	chr15:73343816-73343863	HepG2	liver:	n/a	n/a
22	CHD2	chr15:73345440-73345815	HepG2	liver:	n/a	chr15:73345643-73345653
23	CHD2	chr15:73344310-73344581	GM12878	blood:	n/a	chr15:73344408-73344418
24	CHD2	chr15:73344328-73344589	HepG2	liver:	n/a	chr15:73344408-73344418
25	CHD2	chr15:73345361-73345649	GM12878	blood:	n/a	n/a
26	CHD2	chr15:73343807-73345636	Hela-S3	cervix:	n/a	chr15:73344408-73344418 chr15:73344807-73344817
27	CREB1	chr15:73344299-73344577	A549	lung:	n/a	n/a
28	CREB1	chr15:73344743-73345058	A549	lung:	n/a	n/a
29	CREB1	chr15:73344081-73344942	HepG2	liver:	n/a	n/a
30	CREB1	chr15:73344208-73344620	H1-hESC	embryonic stem cell:	n/a	n/a
31	CREB1	chr15:73344043-73344623	H1-hESC	embryonic stem cell:	n/a	n/a
32	CREB1	chr15:73344123-73344736	A549	lung:	n/a	n/a
33	CTBP2	chr15:73343836-73344538	H1-hESC	embryonic stem cell:	n/a	n/a
34	CTCF	chr15:73345460-73345610	GM06990	blood:	n/a	chr15:73345483-73345504 chr15:73345481-73345499
35	CTCF	chr15:73345420-73345570	HPAF	blood vessel:	n/a	chr15:73345483-73345504 chr15:73345481-73345499
36	CTCF	chr15:73344920-73345030	GM19239	blood:	n/a	n/a
37	CTCF	chr15:73345440-73345590	AoAF	blood vessel:	n/a	chr15:73345483-73345504 chr15:73345481-73345499
38	CTCF	chr15:73345312-73345576	Hela-S3	cervix:	n/a	chr15:73345483-73345504 chr15:73345481-73345499
39	CTCF	chr15:73345340-73345490	HCM	heart:	n/a	n/a
40	CTCF	chr15:73345300-73345450	HCT-116	colon:	n/a	n/a
41	CTCF	chr15:73345320-73345470	SK-N-SH_RA	brain:	n/a	n/a
42	CTCF	chr15:73345160-73345675	K562	blood:	n/a	chr15:73345483-73345504 chr15:73345481-73345499
43	CTCF	chr15:73344940-73345090	HCPEpiC	choroid plexus:	n/a	n/a
44	CTCF	chr15:73345340-73345490	SK-N-SH_RA	brain:	n/a	n/a
45	CTCF	chr15:73345480-73345630	GM12865	blood:	n/a	chr15:73345483-73345504 chr15:73345481-73345499
46	CTCF	chr15:73345360-73345510	GM12870	blood:	n/a	chr15:73345483-73345504 chr15:73345481-73345499
47	CTCF	chr15:73345480-73345630	GM12872	blood:	n/a	chr15:73345483-73345504 chr15:73345481-73345499
48	CTCF	chr15:73345580-73345730	GM12871	blood:	n/a	n/a
49	CTCF	chr15:73345471-73345548	HUVEC	blood vessel:	n/a	chr15:73345483-73345504 chr15:73345481-73345499
50	CTCF	chr15:73345600-73345750	BE2_C	brain:	n/a	n/a

(count:672 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:73343567-73343617	HMEC	breast:	n/a
2	chr15:73343567-73343617	HMEC	breast:	n/a
3	chr15:73345745-73345795	T-47D	breast:	n/a
4	chr15:73345666-73345716	SK-N-SH_RA	brain:	n/a
5	chr15:73343980-73344030	ECC-1	luminal epithelium:	n/a
6	chr15:73345666-73345716	GM12891	blood:	n/a
7	chr15:73344252-73344302	Jurkat	blood:	n/a
8	chr15:73345607-73345657	HCF	heart:	n/a
9	chr15:73344233-73344283	ECC-1	luminal epithelium:	n/a
10	chr15:73344233-73344283	HAEpiC	amniotic membrane:	n/a
11	chr15:73343567-73343617	MCF-7	breast:	n/a
12	chr15:73343567-73343617	T-47D	breast:	n/a
13	chr15:73345745-73345795	HPAEpiC	pulmonary alveolar:	n/a
14	chr15:73345745-73345795	SK-N-MC	brain:	n/a
15	chr15:73343980-73344030	HCF	heart:	n/a
16	chr15:73343567-73343617	ProgFib	skin:	n/a
17	chr15:73345212-73345262	HL-60	blood:	n/a
18	chr15:73343980-73344030	PFSK-1	brain:	n/a
19	chr15:73343980-73344030	AoSMC	blood vessel:	n/a
20	chr15:73345666-73345716	HCPEpiC	choroid plexus:	n/a
21	chr15:73343567-73343617	HCPEpiC	choroid plexus:	n/a
22	chr15:73343567-73343617	HCT-116	colon:	n/a
23	chr15:73344233-73344283	NB4	blood:	n/a
24	chr15:73344290-73344340	PFSK-1	brain:	n/a
25	chr15:73344290-73344340	BE2_C	brain:	n/a
26	chr15:73345745-73345795	K562	blood:	n/a
27	chr15:73345607-73345657	HUVEC	blood vessel:	n/a
28	chr15:73345212-73345262	NT2-D1	testis:	n/a
29	chr15:73345368-73345418	NH-A	brain:	n/a
30	chr15:73344233-73344283	HCPEpiC	choroid plexus:	n/a
31	chr15:73343980-73344030	HEEpiC	esophagus:	n/a
32	chr15:73345212-73345262	BE2_C	brain:	n/a
33	chr15:73344233-73344283	NT2-D1	testis:	n/a
34	chr15:73345212-73345262	RPTEC	kidney:	n/a
35	chr15:73344867-73344917	HCF	heart:	n/a
36	chr15:73344867-73344917	MCF-7	breast:	n/a
37	chr15:73345212-73345262	HCPEpiC	choroid plexus:	n/a
38	chr15:73343980-73344030	SK-N-SH_RA	brain:	n/a
39	chr15:73344867-73344917	HUVEC	blood vessel:	n/a
40	chr15:73344252-73344302	HPAEpiC	pulmonary alveolar:	n/a
41	chr15:73343980-73344030	HNPCEpiC	eye:	n/a
42	chr15:73345212-73345262	ProgFib	skin:	n/a
43	chr15:73344867-73344917	U87	brain:	n/a
44	chr15:73344233-73344283	GM12878	blood:	n/a
45	chr15:73345745-73345795	HIPEpiC	eye:	n/a
46	chr15:73344252-73344302	BE2_C	brain:	n/a
47	chr15:73344252-73344302	ECC-1	luminal epithelium:	n/a
48	chr15:73343567-73343617	K562	blood:	n/a
49	chr15:73345607-73345657	HIPEpiC	eye:	n/a
50	chr15:73345212-73345262	Caco-2	colon:	n/a

(count:4 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:72765203..72766825-chr15:73342381..73345092,2	MCF-7	breast:
2	chr15:73074691..73078350-chr15:73341676..73346479,5	MCF-7	breast:
3	chr15:73344178..73344781-chr9:7799223..7800164,2	HCT-116	colon:
4	chr15:73075212..73078087-chr15:73342810..73345457,4	MCF-7	breast:

No data

Variant related genes	Relation type
NEO1	TF binding region
NEO1	CpG island
ENSG00000166233	chromatin interactions
ENSG00000159322	chromatin interactions
ENSG00000137038	chromatin interactions
ENSG00000261423	chromatin interactions
ENSG00000260898	chromatin interactions

Extended variants
information (count: 107 )
Associated
traits (count: 70 )

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	rs547953293	chr15:73343426-73343427	Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
2	rs62016792	chr15:73343440-73343441	Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
3	rs536469024	chr15:73343501-73343502	Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
4	rs374487183	chr15:73343536-73343537	Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
5	rs191547043	chr15:73343538-73343539	Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
6	rs567030637	chr15:73343564-73343565	Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
7	rs141982291	chr15:73343576-73343577	Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
8	rs75743821	chr15:73343580-73343581	Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
9	rs184377410	chr15:73343594-73343595	Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
10	rs555933027	chr15:73343607-73343608	Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
11	rs77667665	chr15:73343619-73343620	Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
12	rs66466251	chr15:73343649-73343650	Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs188916990	chr15:73343665-73343666	Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
14	rs145171685	chr15:73343697-73343698	Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
15	rs369591981	chr15:73343708-73343709	Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
16	rs148490120	chr15:73343724-73343725	Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
17	rs561328256	chr15:73343729-73343730	Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
18	rs79302459	chr15:73343754-73343755	Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
19	rs142706434	chr15:73343778-73343779	Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
20	rs375625400	chr15:73343808-73343809	Active TSS Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
21	rs543798705	chr15:73343827-73343828	Active TSS Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
22	rs193290685	chr15:73343839-73343840	Active TSS Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
23	rs532551578	chr15:73343919-73343920	Active TSS Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
24	rs547743429	chr15:73343921-73343922	Active TSS Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
25	rs559621395	chr15:73343966-73343967	Active TSS Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
26	rs368395431	chr15:73343970-73343971	Active TSS Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
27	rs548413473	chr15:73343978-73343979	Active TSS Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
28	rs546217205	chr15:73344024-73344025	Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
29	rs537571075	chr15:73344044-73344045	Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
30	rs549734482	chr15:73344047-73344048	Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
31	rs571122305	chr15:73344090-73344091	Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
32	rs62016793	chr15:73344196-73344197	Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs554062672	chr15:73344213-73344214	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
34	rs572381458	chr15:73344264-73344265	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
35	rs536443632	chr15:73344278-73344279	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
36	rs116688915	chr15:73344293-73344294	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
37	rs576462762	chr15:73344332-73344333	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
38	rs7165809	chr15:73344499-73344500	Active TSS Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
39	rs8027235	chr15:73344505-73344506	Active TSS Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
40	rs113368980	chr15:73344527-73344528	Active TSS Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
41	rs8027278	chr15:73344570-73344571	Active TSS Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
42	rs8031255	chr15:73344632-73344633	Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
43	rs528003048	chr15:73344639-73344640	Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
44	rs543514893	chr15:73344750-73344751	Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
45	rs565399234	chr15:73344753-73344754	Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
46	rs112680211	chr15:73344761-73344762	Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
47	rs577116019	chr15:73344816-73344817	Active TSS Bivalent/Poised TSS Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
48	rs1131850	chr15:73345115-73345116	Active TSS Bivalent/Poised TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs541034605	chr15:73345149-73345150	Active TSS Bivalent/Poised TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs559608695	chr15:73345214-73345215	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:70)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	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
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
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Multiple myeloma	20724749	CNVD
Lung cancer	18438408	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Cancer	16751803	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Breast cancer	17133270	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Prostate cancer	16573809	CNVD
Autism	17322880	CNVD
phobic disorder	16773131	CNVD
Autism	21480499	CNVD
Disorders of sex development	22290220	CNVD
Mental retardation	19951919	CNVD
Mental retardation	16773131	CNVD
T-cell lymphomas	19863542	CNVD
15q24 microdeletion syndrome	22180641	CNVD
15q24 microdeletion syndrome	19921647	CNVD
Disease	22216833	CNVD
Mental retardation	17360722	CNVD
15q24 microdeletion syndrome	22216833	CNVD
15q24 microdeletion syndrome	22283845	CNVD
Developmental delay	17932688	CNVD
craniofacial dysmorphism	17932688	CNVD
digital and genital abnormalities	17932688	CNVD
Mental retardation	17621639	CNVD
Breast cancer	21364760	CNVD
Urothelial carcinoma	21177765	CNVD
Epilepsy	22083797	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:443 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:73339400-73343600	Weak transcription	Pancreas	Pancrea
2	chr15:73342000-73343600	Weak transcription	Fetal Stomach	stomach
3	chr15:73342600-73343600	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr15:73343000-73346000	Active TSS	Pancreatic Islets	Pancreatic Islet
5	chr15:73343200-73343600	Flanking Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
6	chr15:73343200-73343600	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
7	chr15:73343200-73343600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
8	chr15:73343200-73343600	Flanking Active TSS	Fetal Brain Female	brain
9	chr15:73343200-73343600	Enhancers	Fetal Heart	heart
10	chr15:73343200-73343600	Flanking Active TSS	Fetal Intestine Large	intestine
11	chr15:73343200-73343600	Enhancers	Rectal Smooth Muscle	rectum
12	chr15:73343200-73343600	Active TSS	Skeletal Muscle Female	skeletal muscle
13	chr15:73343200-73343600	Flanking Bivalent TSS/Enh	HepG2	liver
14	chr15:73343200-73343800	Flanking Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr15:73343200-73343800	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
16	chr15:73343200-73343800	Flanking Active TSS	Fetal Lung	lung
17	chr15:73343200-73343800	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
18	chr15:73343200-73344000	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
19	chr15:73343200-73345800	Active TSS	Breast Myoepithelial Primary Cells	Breast
20	chr15:73343200-73346000	Active TSS	ES-WA7 Cell Line	embryonic stem cell
21	chr15:73343200-73346000	Active TSS	Brain Anterior Caudate	brain
22	chr15:73343200-73346200	Active TSS	Brain Inferior Temporal Lobe	brain
23	chr15:73343200-73346400	Active TSS	H1 Cell Line	embryonic stem cell
24	chr15:73343200-73346400	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
25	chr15:73343200-73346400	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
26	chr15:73343200-73346600	Active TSS	HUES6 Cell Line	embryonic stem cell
27	chr15:73343200-73347600	Active TSS	Colonic Mucosa	Colon
28	chr15:73343400-73343600	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
29	chr15:73343400-73343600	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
30	chr15:73343400-73343600	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
31	chr15:73343400-73343600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
32	chr15:73343400-73343600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
33	chr15:73343400-73343600	Enhancers	Primary T helper cells PMA-I stimulated	--
34	chr15:73343400-73343600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
35	chr15:73343400-73343600	Bivalent Enhancer	Primary T regulatory cells fromperipheralblood	blood
36	chr15:73343400-73343600	Bivalent Enhancer	Primary T killer naive cells fromperipheralblood	blood
37	chr15:73343400-73343600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
38	chr15:73343400-73343600	Flanking Active TSS	Brain Hippocampus Middle	brain
39	chr15:73343400-73343600	Enhancers	Brain Substantia Nigra	brain
40	chr15:73343400-73343600	Flanking Active TSS	Colon Smooth Muscle	Colon
41	chr15:73343400-73343600	Enhancers	Duodenum Smooth Muscle	Duodenum
42	chr15:73343400-73343600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
43	chr15:73343400-73343600	Flanking Active TSS	Fetal Intestine Small	intestine
44	chr15:73343400-73343600	Bivalent/Poised TSS	Fetal Muscle Leg	muscle
45	chr15:73343400-73343600	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
46	chr15:73343400-73343600	Active TSS	HMEC	breast
47	chr15:73343400-73343800	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
48	chr15:73343400-73343800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
49	chr15:73343400-73343800	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
50	chr15:73343400-73343800	Flanking Active TSS	Adipose Nuclei	Adipose

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