Variant report

Variant	nsv568776
Chromosome Location	chr15:31617788-31620435
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:31618589-31618992	K562	blood:	n/a	n/a
2	ARID3A	chr15:31618550-31618737	HepG2	liver:	n/a	n/a
3	ATF1	chr15:31618502-31618980	K562	blood:	n/a	n/a
4	ATF2	chr15:31617290-31617914	GM12878	blood:	n/a	n/a
5	ATF2	chr15:31618283-31619194	GM12878	blood:	n/a	chr15:31618978-31618992
6	ATF3	chr15:31618605-31619046	K562	blood:	n/a	chr15:31618970-31618990 chr15:31618976-31618990 chr15:31618669-31618679 chr15:31618905-31618914
7	BACH1	chr15:31618840-31621115	H1-hESC	embryonic stem cell:	n/a	n/a
8	BCL3	chr15:31617847-31618839	A549	lung:	n/a	chr15:31617883-31617896 chr15:31617885-31617898 chr15:31618149-31618162 chr15:31618360-31618373 chr15:31618099-31618112 chr15:31618424-31618433 chr15:31618661-31618670 chr15:31618494-31618507 chr15:31618416-31618429 chr15:31618212-31618225 chr15:31618612-31618625
9	BCL3	chr15:31617942-31619239	GM12878	blood:	n/a	chr15:31618938-31618947 chr15:31618149-31618162 chr15:31618933-31618946 chr15:31618360-31618373 chr15:31618099-31618112 chr15:31618424-31618433 chr15:31618661-31618670 chr15:31618494-31618507 chr15:31618416-31618429 chr15:31618932-31618945 chr15:31618212-31618225 chr15:31618935-31618948 chr15:31618612-31618625
10	BCLAF1	chr15:31616995-31617967	GM12878	blood:	n/a	chr15:31617883-31617896 chr15:31617885-31617898 chr15:31617222-31617229
11	BCLAF1	chr15:31616819-31619281	GM12878	blood:	n/a	chr15:31617883-31617896 chr15:31618938-31618947 chr15:31617885-31617898 chr15:31618149-31618162 chr15:31618933-31618946 chr15:31618360-31618373 chr15:31619243-31619256 chr15:31618099-31618112 chr15:31618424-31618433 chr15:31618661-31618670 chr15:31618494-31618507 chr15:31618416-31618429 chr15:31618932-31618945 chr15:31618212-31618225 chr15:31618935-31618948 chr15:31617222-31617229 chr15:31618612-31618625
12	BCLAF1	chr15:31617969-31618750	GM12878	blood:	n/a	chr15:31618149-31618162 chr15:31618360-31618373 chr15:31618099-31618112 chr15:31618424-31618433 chr15:31618661-31618670 chr15:31618494-31618507 chr15:31618416-31618429 chr15:31618212-31618225 chr15:31618612-31618625
13	BHLHE40	chr15:31618121-31619637	GM12878	blood:	n/a	chr15:31619262-31619278 chr15:31618319-31618335 chr15:31618143-31618159 chr15:31618422-31618438 chr15:31618932-31618948 chr15:31619050-31619066 chr15:31619154-31619170
14	BHLHE40	chr15:31618246-31621387	K562	blood:	n/a	chr15:31621042-31621051 chr15:31621041-31621054 chr15:31619262-31619278 chr15:31618319-31618335 chr15:31618422-31618438 chr15:31621037-31621058 chr15:31621044-31621053 chr15:31620807-31620823 chr15:31620142-31620158 chr15:31618932-31618948 chr15:31619050-31619066 chr15:31620315-31620331 chr15:31619154-31619170 chr15:31620821-31620837
15	BHLHE40	chr15:31620283-31621504	HepG2	liver:	n/a	chr15:31621042-31621051 chr15:31621041-31621054 chr15:31621037-31621058 chr15:31621044-31621053 chr15:31620807-31620823 chr15:31620315-31620331 chr15:31620821-31620837
16	BHLHE40	chr15:31618206-31619189	HepG2	liver:	n/a	chr15:31618319-31618335 chr15:31618422-31618438 chr15:31618932-31618948 chr15:31619050-31619066 chr15:31619154-31619170
17	BHLHE40	chr15:31619930-31622070	GM12878	blood:	n/a	chr15:31621042-31621051 chr15:31621041-31621054 chr15:31621037-31621058 chr15:31621044-31621053 chr15:31620807-31620823 chr15:31620142-31620158 chr15:31620315-31620331 chr15:31620821-31620837
18	BHLHE40	chr15:31617318-31617910	GM12878	blood:	n/a	n/a
19	BRCA1	chr15:31618323-31618891	Hela-S3	cervix:	n/a	n/a
20	BRCA1	chr15:31618538-31618564	HepG2	liver:	n/a	n/a
21	CCNT2	chr15:31617711-31620924	K562	blood:	n/a	chr15:31618905-31618914 chr15:31617900-31617909 chr15:31620285-31620294
22	CEBPB	chr15:31618305-31619136	Hela-S3	cervix:	n/a	n/a
23	CEBPD	chr15:31618402-31619106	HepG2	liver:	n/a	n/a
24	CEBPD	chr15:31619984-31620619	HepG2	liver:	n/a	n/a
25	CHD1	chr15:31616631-31618762	GM12878	blood:	n/a	n/a
26	CHD1	chr15:31617210-31621792	IMR90	lung:	n/a	chr15:31620036-31620046 chr15:31620162-31620172 chr15:31620076-31620086 chr15:31620113-31620123
27	CHD1	chr15:31620349-31621401	GM12878	blood:	n/a	n/a
28	CHD1	chr15:31618979-31620122	GM12878	blood:	n/a	chr15:31620036-31620046 chr15:31620076-31620086
29	CHD2	chr15:31619810-31620094	GM12878	blood:	n/a	chr15:31620036-31620046 chr15:31620076-31620086
30	CHD2	chr15:31618484-31618982	K562	blood:	n/a	n/a
31	CHD2	chr15:31617045-31619545	GM12878	blood:	n/a	n/a
32	CHD2	chr15:31617575-31619605	Hela-S3	cervix:	n/a	n/a
33	CHD2	chr15:31619939-31620667	Hela-S3	cervix:	n/a	chr15:31620036-31620046 chr15:31620162-31620172 chr15:31620076-31620086 chr15:31620113-31620123
34	CHD2	chr15:31617854-31617859	K562	blood:	n/a	n/a
35	CHD2	chr15:31620294-31621673	GM12878	blood:	n/a	n/a
36	CHD2	chr15:31618203-31619255	HepG2	liver:	n/a	n/a
37	CHD2	chr15:31618493-31619111	H1-hESC	embryonic stem cell:	n/a	n/a
38	CREB1	chr15:31619885-31620727	A549	lung:	n/a	n/a
39	CREB1	chr15:31617672-31619746	A549	lung:	n/a	n/a
40	CREB1	chr15:31617951-31619515	HepG2	liver:	n/a	n/a
41	CREB1	chr15:31618444-31618928	ECC-1	luminal epithelium:	n/a	n/a
42	CREB1	chr15:31618381-31619215	H1-hESC	embryonic stem cell:	n/a	n/a
43	CREB1	chr15:31618287-31619461	H1-hESC	embryonic stem cell:	n/a	n/a
44	CREB1	chr15:31618466-31619104	A549	lung:	n/a	n/a
45	CREB1	chr15:31618365-31619455	K562	blood:	n/a	n/a
46	CREB1	chr15:31617727-31619445	GM12878	blood:	n/a	n/a
47	CREB1	chr15:31620169-31621234	GM12878	blood:	n/a	n/a
48	CREB1	chr15:31618364-31619213	K562	blood:	n/a	n/a
49	CTBP2	chr15:31618065-31619538	H1-hESC	embryonic stem cell:	n/a	n/a
50	CTCF	chr15:31619542-31619546	GM19239	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:31617764-31617814	AG09319	gingival:	n/a
2	chr15:31619006-31619056	K562	blood:	n/a
3	chr15:31620290-31620340	H1-hESC	embryonic stem cell:	embryo
4	chr15:31620290-31620340	SK-N-MC	brain:	n/a
5	chr15:31618618-31618668	HL-60	blood:	n/a
6	chr15:31619399-31619449	NT2-D1	testis:	n/a
7	chr15:31620290-31620340	NH-A	brain:	n/a
8	chr15:31619396-31619446	PrEC	prostate:	n/a
9	chr15:31620290-31620340	HCF	heart:	n/a
10	chr15:31619396-31619446	T-47D	breast:	n/a
11	chr15:31619396-31619446	SK-N-SH_RA	brain:	n/a
12	chr15:31619006-31619056	IMR90	lung:	fetal
13	chr15:31619949-31619999	NHDF-neo	bronchial:	n/a
14	chr15:31620290-31620340	PFSK-1	brain:	n/a
15	chr15:31620290-31620340	HCPEpiC	choroid plexus:	n/a
16	chr15:31619006-31619056	NB4	blood:	n/a
17	chr15:31617764-31617814	HRE	kidney:	n/a
18	chr15:31618618-31618668	HCF	heart:	n/a
19	chr15:31617764-31617814	HAEpiC	amniotic membrane:	n/a
20	chr15:31618618-31618668	BE2_C	brain:	n/a
21	chr15:31617764-31617814	U87	brain:	n/a
22	chr15:31620290-31620340	AG09319	gingival:	n/a
23	chr15:31619399-31619449	SKMC	muscle:	n/a
24	chr15:31618604-31618654	MCF-7	breast:	n/a
25	chr15:31618604-31618654	ProgFib	skin:	n/a
26	chr15:31618618-31618668	PANC-1	pancreas:	n/a
27	chr15:31618604-31618654	HCT-116	colon:	n/a
28	chr15:31617764-31617814	LNCaP	prostate:	n/a
29	chr15:31619006-31619056	CMK	blood:	n/a
30	chr15:31619949-31619999	ovcar-3	ovarian:	n/a
31	chr15:31618604-31618654	HUVEC	blood vessel:	n/a
32	chr15:31619949-31619999	H1-hESC	embryonic stem cell:	embryo
33	chr15:31618618-31618668	SKMC	muscle:	n/a
34	chr15:31618604-31618654	GM12878	blood:	n/a
35	chr15:31618604-31618654	AG09309	skin:	n/a
36	chr15:31619006-31619056	U87	brain:	n/a
37	chr15:31619949-31619999	GM12878	blood:	n/a
38	chr15:31619396-31619446	GM12892	blood:	n/a
39	chr15:31618618-31618668	NH-A	brain:	n/a
40	chr15:31618618-31618668	GM12878	blood:	n/a
41	chr15:31619399-31619449	Caco-2	colon:	n/a
42	chr15:31619949-31619999	PANC-1	pancreas:	n/a
43	chr15:31618604-31618654	T-47D	breast:	n/a
44	chr15:31619399-31619449	HIPEpiC	eye:	n/a
45	chr15:31618604-31618654	HEEpiC	esophagus:	n/a
46	chr15:31619006-31619056	NHBE	bronchial:	n/a
47	chr15:31619399-31619449	AG10803	skin:	n/a
48	chr15:31617764-31617814	HPAEpiC	pulmonary alveolar:	n/a
49	chr15:31619399-31619449	HPAEpiC	pulmonary alveolar:	n/a
50	chr15:31619399-31619449	SAEC	small airway:	n/a

No.	Distal block	Cell Line	Cell type
1	chr15:31618617..31619175-chr17:76920900..76921481,2	Hela-S3	cervix:
2	chr15:31618838..31621702-chr15:31631313..31632972,2	MCF-7	breast:
3	chr15:31618837..31619492-chr17:8286314..8286908,2	Hela-S3	cervix:
4	chr15:31619043..31619728-chr17:62340009..62340776,2	Hela-S3	cervix:
5	chr15:31618609..31619470-chr7:143077778..143078496,2	Hela-S3	cervix:
6	chr15:31618253..31621608-chr15:31655043..31658553,3	K562	blood:
7	chr15:31608249..31610861-chr15:31620080..31623099,3	K562	blood:
8	chr15:31619684..31620471-chr16:30709793..30710319,2	Hela-S3	cervix:
9	chr15:31618649..31619470-chr7:86781497..86782119,2	Hela-S3	cervix:
10	chr15:31618168..31621382-chr15:31631982..31634646,4	MCF-7	breast:
11	chr15:31620067..31620789-chr15:31727225..31727966,3	MCF-7	breast:
12	chr15:31507074..31509248-chr15:31619187..31621529,2	MCF-7	breast:
13	chr15:31618149..31620497-chr15:31657004..31658970,2	MCF-7	breast:
14	chr15:31619156..31619701-chr5:40678819..40679598,2	Hela-S3	cervix:
15	chr15:31617830..31618662-chr8:43094478..43095043,2	MCF-7	breast:
16	chr15:31618668..31619569-chr2:9770552..9771168,2	HCT-116	colon:
17	chr15:31619962..31620883-chr7:26239738..26240418,2	Hela-S3	cervix:
18	chr15:31616920..31619586-chr8:103667733..103670691,2	MCF-7	breast:
19	chr15:31507690..31508326-chr15:31619594..31620115,2	MCF-7	breast:
20	chr15:31615054..31617899-chr15:31634755..31636481,2	MCF-7	breast:
21	chr15:31507333..31508207-chr15:31618137..31618644,2	MCF-7	breast:
22	chr15:31616992..31619470-chr15:31682984..31685911,2	K562	blood:
23	chr15:31618754..31620549-chr15:31631588..31633647,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAN1-2	chr15:31619770-31619992	NONHSAT041444

Variant related genes	Relation type
KLF13	TF binding region
KLF13	CpG island
ENSG00000159840	chromatin interactions
ENSG00000122566	chromatin interactions
ENSG00000263809	chromatin interactions
ENSG00000135164	chromatin interactions
ENSG00000259448	chromatin interactions
ENSG00000261840	chromatin interactions
ENSG00000161970	chromatin interactions
ENSG00000155090	chromatin interactions
ENSG00000035862	chromatin interactions
ENSG00000134308	chromatin interactions
ENSG00000224046	chromatin interactions
ENSG00000136478	chromatin interactions
ENSG00000169926	chromatin interactions

Extended variants
information (count: 87 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:87 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6493604	chr15:31617788-31617789	Bivalent/Poised TSS Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs555017158	chr15:31617789-31617790	Bivalent/Poised TSS Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs574687387	chr15:31617791-31617792	Bivalent/Poised TSS Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs543601219	chr15:31617855-31617856	Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs563621651	chr15:31617861-31617862	Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs577187484	chr15:31617865-31617866	Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs8041203	chr15:31617877-31617878	Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs559103713	chr15:31617908-31617909	Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs528063304	chr15:31617927-31617928	Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs73381264	chr15:31617929-31617930	Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs114160484	chr15:31617943-31617944	Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs549956257	chr15:31617959-31617960	Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs570038929	chr15:31617973-31617974	Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs538946932	chr15:31618160-31618161	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs532825438	chr15:31618211-31618212	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs552800144	chr15:31618219-31618220	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs111960531	chr15:31618237-31618238	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs534968657	chr15:31618255-31618256	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs554775549	chr15:31618260-31618261	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs574977004	chr15:31618265-31618266	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs537271216	chr15:31618275-31618276	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs968594	chr15:31618284-31618285	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs577079449	chr15:31618315-31618316	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs371599707	chr15:31618327-31618328	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs559554931	chr15:31618343-31618344	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs572761511	chr15:31618353-31618354	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs541802483	chr15:31618373-31618374	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs375380257	chr15:31618381-31618382	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs530497191	chr15:31618392-31618393	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs368313822	chr15:31618411-31618412	Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs549994633	chr15:31618423-31618424	Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs563554258	chr15:31618424-31618425	Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs183635362	chr15:31618538-31618539	Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs80177425	chr15:31618590-31618591	Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs566322263	chr15:31618591-31618592	Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs555186968	chr15:31618620-31618621	Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
37	rs534750004	chr15:31618638-31618639	Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
38	rs150793629	chr15:31618641-31618642	Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
39	rs548581029	chr15:31618642-31618643	Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
40	rs188522489	chr15:31618658-31618659	Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
41	rs74409869	chr15:31618659-31618660	Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
42	rs557464963	chr15:31618663-31618664	Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
43	rs2082976	chr15:31618670-31618671	Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
44	rs539580436	chr15:31618684-31618685	Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
45	rs553035785	chr15:31618689-31618690	Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
46	rs150608458	chr15:31618692-31618693	Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
47	rs573091810	chr15:31618755-31618756	Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
48	rs371450808	chr15:31618780-31618781	Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
49	rs541487002	chr15:31618797-31618798	Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
50	rs2099545	chr15:31618939-31618940	Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:90)

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
Hodgkin''s lymphoma	18641027	CNVD
Melanoma	18172304	CNVD
Autism	17322880	CNVD
Prader-willi syndrome	19329560	CNVD
Autism	17999366	CNVD
Autism	17901113	CNVD
Neurodevelopmental disorder	17015230	CNVD
Autism	18414403	CNVD
Neurocytoma	17123091	CNVD
Mental retardation	18923513	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
Gastrointestinal stromal cancer	20818650	CNVD
Intellectual disability	22102821	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	20729466	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Breast cancer	17133270	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
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21785460	CNVD
Prostate cancer	18632612	CNVD
Abnormal corpus callosum	21572526	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Autism	19204725	CNVD
Schizophrenia	19204725	CNVD
Schizophrenia	19149910	CNVD
Ovarian cancer	22174824	CNVD
Epilepsy	20502679	CNVD
small cell lung cancer	20016488	CNVD
Autism	19521722	CNVD
Bipolar disorder	19114987	CNVD
Epilepsy	19521722	CNVD
Mental retardation	19521722	CNVD
Schizophrenia	19521646	CNVD
Autism	19050728	CNVD
Schizophrenia	19348701	CNVD
Schizophrenia	18668039	CNVD
Schizophrenia	18990708	CNVD
Schizophrenia	19571808	CNVD
Velocardiofacial syndrome	19329560	CNVD
Schizophrenia	19443537	CNVD
Epilepsy	20923578	CNVD
Autism	19955444	CNVD
Autism	20964600	CNVD
Schizophrenia	19955444	CNVD
Olfactory neuroblastoma	18408657	CNVD
Pancreatic cancer	17952125	CNVD
Legius syndrome	19443465	CNVD
Holoprosencephaly	21359414	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD

Chromatin state (count:262 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:31615800-31617800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
2	chr15:31616000-31617800	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
3	chr15:31616000-31617800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr15:31616000-31618000	Flanking Active TSS	Primary B cells from cord blood	blood
5	chr15:31616200-31617800	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
6	chr15:31616800-31617800	Flanking Active TSS	Fetal Thymus	thymus
7	chr15:31616800-31617800	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
8	chr15:31616800-31618400	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
9	chr15:31617000-31617800	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr15:31617000-31617800	Flanking Active TSS	Primary T cells from cord blood	blood
11	chr15:31617000-31617800	Flanking Active TSS	Brain Germinal Matrix	brain
12	chr15:31617000-31617800	Flanking Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
13	chr15:31617000-31617800	Flanking Active TSS	Duodenum Mucosa	Duodenum
14	chr15:31617000-31617800	Flanking Active TSS	Fetal Heart	heart
15	chr15:31617000-31617800	Flanking Active TSS	Rectal Smooth Muscle	rectum
16	chr15:31617000-31617800	Flanking Active TSS	Hela-S3	cervix
17	chr15:31617000-31618000	Flanking Active TSS	Primary hematopoietic stem cells	blood
18	chr15:31617000-31618000	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
19	chr15:31617000-31618000	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
20	chr15:31617000-31618000	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
21	chr15:31617200-31617800	Bivalent/Poised TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr15:31617200-31617800	Flanking Bivalent TSS/Enh	HUES64 Cell Line	embryonic stem cell
23	chr15:31617200-31617800	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
24	chr15:31617200-31617800	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
25	chr15:31617200-31617800	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
26	chr15:31617200-31617800	Flanking Active TSS	Muscle Satellite Cultured Cells	--
27	chr15:31617200-31617800	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
28	chr15:31617200-31617800	Flanking Active TSS	Brain Anterior Caudate	brain
29	chr15:31617200-31617800	Flanking Active TSS	Brain Cingulate Gyrus	brain
30	chr15:31617200-31617800	Flanking Active TSS	Brain Hippocampus Middle	brain
31	chr15:31617200-31617800	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
32	chr15:31617200-31617800	Flanking Active TSS	Brain Substantia Nigra	brain
33	chr15:31617200-31617800	Flanking Active TSS	Fetal Kidney	kidney
34	chr15:31617200-31617800	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
35	chr15:31617200-31617800	Flanking Active TSS	HSMMtube	muscle
36	chr15:31617200-31617800	Flanking Active TSS	NHDF-Ad	bronchial
37	chr15:31617200-31618000	Flanking Active TSS	Primary B cells from peripheral blood	blood
38	chr15:31617200-31618000	Flanking Active TSS	Primary T cells fromperipheralblood	blood
39	chr15:31617200-31618000	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
40	chr15:31617200-31618000	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
41	chr15:31617200-31618000	Flanking Active TSS	Primary Natural Killer cells fromperipheralblood	blood
42	chr15:31617200-31618000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
43	chr15:31617200-31618000	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
44	chr15:31617200-31618000	Flanking Active TSS	Adipose Nuclei	Adipose
45	chr15:31617200-31618000	Flanking Active TSS	Fetal Muscle Leg	muscle
46	chr15:31617200-31618000	Active TSS	Right Atrium	heart
47	chr15:31617200-31618000	Flanking Active TSS	Stomach Smooth Muscle	stomach
48	chr15:31617200-31618000	Flanking Active TSS	Dnd41	blood
49	chr15:31617200-31618000	Flanking Active TSS	HSMM	muscle
50	chr15:31617200-31618200	Flanking Active TSS	HMEC	breast

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