Variant report

Variant	nsv904416
Chromosome Location	chr15:77845959-77967416
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2902)
CpG islands
(count:2687)
Chromatin interactive
region (count:194)
LncRNA
region (count:39)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2902 , 50 per page) page: 1 2 3 4 5 6 7 ... 59

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:77947350-77947472	K562	blood:	n/a	n/a
2	ARID3A	chr15:77925899-77926076	K562	blood:	n/a	n/a
3	ARID3A	chr15:77912745-77912914	K562	blood:	n/a	n/a
4	ARID3A	chr15:77942736-77942925	HepG2	liver:	n/a	n/a
5	ARID3A	chr15:77926765-77927030	K562	blood:	n/a	n/a
6	ARID3A	chr15:77861390-77861782	HepG2	liver:	n/a	n/a
7	ARID3A	chr15:77915025-77915043	K562	blood:	n/a	n/a
8	ATF2	chr15:77925461-77927008	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF2	chr15:77915941-77916411	H1-hESC	embryonic stem cell:	n/a	n/a
10	ATF2	chr15:77925762-77927046	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF2	chr15:77915698-77916516	H1-hESC	embryonic stem cell:	n/a	n/a
12	ATF3	chr15:77892250-77892522	K562	blood:	n/a	n/a
13	ATF3	chr15:77925857-77926179	GM12878	blood:	n/a	n/a
14	ATF3	chr15:77885188-77885374	K562	blood:	n/a	n/a
15	ATF3	chr15:77925754-77926241	A549	lung:	n/a	n/a
16	ATF3	chr15:77925817-77926099	H1-hESC	embryonic stem cell:	n/a	n/a
17	ATF3	chr15:77942662-77942999	K562	blood:	n/a	n/a
18	ATF3	chr15:77925732-77926191	H1-hESC	embryonic stem cell:	n/a	n/a
19	ATF3	chr15:77925816-77926085	K562	blood:	n/a	n/a
20	BACH1	chr15:77925619-77926520	H1-hESC	embryonic stem cell:	n/a	n/a
21	BACH1	chr15:77926761-77927026	H1-hESC	embryonic stem cell:	n/a	n/a
22	BACH1	chr15:77899147-77899415	H1-hESC	embryonic stem cell:	n/a	n/a
23	BACH1	chr15:77897153-77897255	H1-hESC	embryonic stem cell:	n/a	n/a
24	BACH1	chr15:77915577-77915777	H1-hESC	embryonic stem cell:	n/a	n/a
25	BCL3	chr15:77925412-77926262	A549	lung:	n/a	chr15:77925420-77925433
26	BCL3	chr15:77845554-77846010	GM12878	blood:	n/a	chr15:77845994-77846007
27	BCLAF1	chr15:77925756-77926123	GM12878	blood:	n/a	n/a
28	BCLAF1	chr15:77925737-77926107	GM12878	blood:	n/a	n/a
29	BHLHE40	chr15:77925559-77926179	K562	blood:	n/a	n/a
30	BHLHE40	chr15:77925834-77926167	GM12878	blood:	n/a	n/a
31	BHLHE40	chr15:77914524-77915734	K562	blood:	n/a	n/a
32	BHLHE40	chr15:77849561-77849608	K562	blood:	n/a	n/a
33	BHLHE40	chr15:77876682-77876905	K562	blood:	n/a	n/a
34	BHLHE40	chr15:77904325-77904461	K562	blood:	n/a	n/a
35	BHLHE40	chr15:77849986-77850257	K562	blood:	n/a	n/a
36	BHLHE40	chr15:77952152-77952423	K562	blood:	n/a	n/a
37	BHLHE40	chr15:77912708-77912955	K562	blood:	n/a	n/a
38	BHLHE40	chr15:77922594-77922636	K562	blood:	n/a	n/a
39	BHLHE40	chr15:77899292-77899363	K562	blood:	n/a	n/a
40	BHLHE40	chr15:77869841-77869966	K562	blood:	n/a	n/a
41	BHLHE40	chr15:77901103-77901302	K562	blood:	n/a	n/a
42	BHLHE40	chr15:77947378-77947705	K562	blood:	n/a	n/a
43	BHLHE40	chr15:77950692-77950878	HepG2	liver:	n/a	n/a
44	BHLHE40	chr15:77926780-77927016	K562	blood:	n/a	n/a
45	BRCA1	chr15:77925929-77926145	GM12878	blood:	n/a	n/a
46	BRCA1	chr15:77925788-77926457	H1-hESC	embryonic stem cell:	n/a	n/a
47	BRCA1	chr15:77925889-77926125	Hela-S3	cervix:	n/a	n/a
48	CBX3	chr15:77926671-77927062	K562	blood:	n/a	n/a
49	CBX3	chr15:77913865-77914196	K562	blood:	n/a	n/a
50	CBX3	chr15:77897291-77897710	K562	blood:	n/a	n/a

(count:2687 , 50 per page) page: 1 2 3 4 5 6 7 ... 54

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:77898183-77898233	Hela-S3	cervix:	n/a
2	chr15:77852897-77852947	HRE	kidney:	n/a
3	chr15:77925892-77925942	Hela-S3	cervix:	n/a
4	chr15:77898183-77898233	Hela-S3	cervix:	n/a
5	chr15:77852897-77852947	HRE	kidney:	n/a
6	chr15:77925892-77925942	Hela-S3	cervix:	n/a
7	chr15:77925481-77925531	HL-60	blood:	n/a
8	chr15:77962173-77962223	IMR90	lung:	fetal
9	chr15:77927358-77927408	PrEC	prostate:	n/a
10	chr15:77927305-77927355	MCF10A-Er-Src	breast:	n/a
11	chr15:77933917-77933967	GM12878	blood:	n/a
12	chr15:77962173-77962223	HMEC	breast:	n/a
13	chr15:77852711-77852761	SKMC	muscle:	n/a
14	chr15:77861673-77861723	SK-N-MC	brain:	n/a
15	chr15:77915770-77915820	HPAEpiC	pulmonary alveolar:	n/a
16	chr15:77898183-77898233	PrEC	prostate:	n/a
17	chr15:77897206-77897256	HNPCEpiC	eye:	n/a
18	chr15:77962173-77962223	HCT-116	colon:	n/a
19	chr15:77925481-77925531	AG09309	skin:	n/a
20	chr15:77933790-77933840	AG04450	lung:	fetal
21	chr15:77862098-77862148	SAEC	small airway:	n/a
22	chr15:77852711-77852761	HEEpiC	esophagus:	n/a
23	chr15:77852897-77852947	HCT-116	colon:	n/a
24	chr15:77922677-77922727	LNCaP	prostate:	n/a
25	chr15:77849740-77849790	SK-N-MC	brain:	n/a
26	chr15:77862098-77862148	HCM	heart:	n/a
27	chr15:77929666-77929716	U87	brain:	n/a
28	chr15:77929666-77929716	HepG2	liver:	n/a
29	chr15:77906127-77906177	NT2-D1	testis:	n/a
30	chr15:77956125-77956175	PANC-1	pancreas:	n/a
31	chr15:77924281-77924331	MCF10A-Er-Src	breast:	n/a
32	chr15:77933785-77933835	AG09319	gingival:	n/a
33	chr15:77908135-77908185	K562	blood:	n/a
34	chr15:77962173-77962223	Hepatocyte	liver:	n/a
35	chr15:77922163-77922213	IMR90	lung:	fetal
36	chr15:77899670-77899720	GM12891	blood:	n/a
37	chr15:77922163-77922213	PFSK-1	brain:	n/a
38	chr15:77906127-77906177	AoSMC	blood vessel:	n/a
39	chr15:77897206-77897256	SKMC	muscle:	n/a
40	chr15:77927358-77927408	HUVEC	blood vessel:	n/a
41	chr15:77889974-77890024	K562	blood:	n/a
42	chr15:77922163-77922213	HCT-116	colon:	n/a
43	chr15:77908135-77908185	HMEC	breast:	n/a
44	chr15:77889974-77890024	HCF	heart:	n/a
45	chr15:77889974-77890024	GM06990	blood:	n/a
46	chr15:77876657-77876707	NT2-D1	testis:	n/a
47	chr15:77889974-77890024	SKMC	muscle:	n/a
48	chr15:77928919-77928969	T-47D	breast:	n/a
49	chr15:77929666-77929716	HCT-116	colon:	n/a
50	chr15:77852711-77852761	U87	brain:	n/a

(count:194 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type
1	chr15:77893403..77895031-chr15:77900449..77902980,2	K562	blood:
2	chr15:77927525..77929710-chr15:77946068..77948764,2	K562	blood:
3	chr15:77950482..77951067-chr15:78113646..78114389,2	K562	blood:
4	chr15:77904241..77907935-chr15:77912354..77915026,5	K562	blood:
5	chr15:77835764..77836461-chr15:77925509..77926265,4	MCF-7	breast:
6	chr15:77861495..77863569-chr15:77924016..77925973,2	K562	blood:
7	chr15:77848268..77851249-chr15:77883793..77885346,2	MCF-7	breast:
8	chr15:77910678..77912184-chr15:77913729..77916491,2	K562	blood:
9	chr15:77952697..77954312-chr15:77961753..77964123,2	K562	blood:
10	chr15:77922761..77925687-chr15:77933695..77936379,3	K562	blood:
11	chr15:77864365..77867025-chr15:77869640..77872108,2	MCF-7	breast:
12	chr15:77923378..77927661-chr15:77939712..77941850,3	MCF-7	breast:
13	chr15:77908642..77910166-chr15:77913466..77916078,2	MCF-7	breast:
14	chr15:77916360..77920054-chr15:77923729..77926072,4	MCF-7	breast:
15	chr15:77925603..77926173-chr15:77946987..77947667,2	MCF-7	breast:
16	chr15:77901988..77905265-chr15:77907024..77909154,3	MCF-7	breast:
17	chr15:77903485..77904267-chr15:77926396..77927267,2	MCF-7	breast:
18	chr15:77927989..77932022-chr15:77933693..77937176,6	K562	blood:
19	chr15:77895225..77896761-chr15:77915510..77917012,2	K562	blood:
20	chr15:77890205..77893278-chr15:77923097..77926362,3	K562	blood:
21	chr15:77914562..77916092-chr15:77921484..77924358,2	MCF-7	breast:
22	chr15:77939682..77942275-chr15:77956399..77958298,2	MCF-7	breast:
23	chr15:77925580..77926309-chr15:78156358..78157211,2	MCF-7	breast:
24	chr15:77914562..77916092-chr15:77921484..77924358,2	MCF-7	breast:
25	chr15:77316379..77317255-chr15:77925626..77926458,2	MCF-7	breast:
26	chr15:77904297..77907501-chr15:77908507..77911725,4	K562	blood:
27	chr15:77951783..77952314-chr15:78066187..78066759,2	MCF-7	breast:
28	chr15:77917075..77919713-chr15:77934421..77936689,2	MCF-7	breast:
29	chr15:77956274..77958726-chr15:77958972..77961104,2	MCF-7	breast:
30	chr15:77884788..77887533-chr15:77890079..77892791,3	K562	blood:
31	chr15:77867409..77870567-chr15:77872173..77875130,4	K562	blood:
32	chr15:77866782..77869407-chr15:77890484..77892735,2	MCF-7	breast:
33	chr15:77916170..77919040-chr15:77941175..77943585,2	K562	blood:
34	chr15:77953192..77954949-chr15:78111776..78113622,2	MCF-7	breast:
35	chr15:77962505..77965298-chr15:77965615..77967291,2	K562	blood:
36	chr15:77410865..77411747-chr15:77876252..77877201,2	MCF-7	breast:
37	chr15:77908642..77910166-chr15:77913466..77916078,2	MCF-7	breast:
38	chr15:77912184..77913186-chr15:77925455..77926450,5	K562	blood:
39	chr15:77926698..77928808-chr15:77930384..77933338,2	K562	blood:
40	chr15:77884388..77887095-chr15:77890695..77892603,2	K562	blood:
41	chr15:77925492..77926460-chr15:77947054..77947731,3	K562	blood:
42	chr15:77925603..77926173-chr15:77946987..77947667,2	MCF-7	breast:
43	chr15:77925509..77926398-chr15:78076937..78077835,4	K562	blood:
44	chr15:77872896..77874517-chr15:77881445..77883437,2	K562	blood:
45	chr15:77876287..77878594-chr15:77925145..77926985,3	K562	blood:
46	chr15:77879443..77881773-chr15:77883698..77885210,2	K562	blood:
47	chr15:77908000..77910749-chr15:77912406..77914677,2	MCF-7	breast:
48	chr15:77925750..77926474-chr15:78007678..78008229,2	MCF-7	breast:
49	chr15:77866782..77869407-chr15:77890484..77892735,2	MCF-7	breast:
50	chr15:77877705..77880943-chr15:77882469..77885198,3	K562	blood:

(count:39 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-HMG20A-4	chr15:77952394-77952525	ENSG00000259281.1
2	lnc-HMG20A-3	chr15:77940181-77941582	ENSG00000259666.1
3	lnc-HMG20A-2	chr15:77864907-77865081	ENSG00000259420.1
4	lnc-HMG20A-2	chr15:77900882-77901023	ENSG00000259420.1
5	lnc-HMG20A-3	chr15:77938650-77938853	NONHSAT047453
6	lnc-HMG20A-4	chr15:77952424-77952507	NONHSAT047457
7	lnc-HMG20A-3	chr15:77943677-77944620	NONHSAT047455
8	lnc-HMG20A-2	chr15:77864593-77864787	ENSG00000259420.1
9	lnc-HMG20A-3	chr15:77938650-77938853	NONHSAT047452
10	lnc-HMG20A-3	chr15:77938684-77938853	ENSG00000259666.1
11	lnc-HMG20A-4	chr15:77959302-77959428	NONHSAT047457
12	lnc-HMG20A-3	chr15:77940560-77940838	NONHSAT047453
13	lnc-HMG20A-3	chr15:77938650-77938853	NONHSAT047451
14	lnc-HMG20A-3	chr15:77938730-77938853	ENSG00000249469
15	lnc-HMG20A-3	chr15:77940486-77940543	ENSG00000259666.1
16	lnc-HMG20A-3	chr15:77943677-77944620	NONHSAT047451
17	lnc-HMG20A-3	chr15:77940181-77940303	ENSG00000259666.1
18	lnc-HMG20A-4	chr15:77952394-77952525	ENSG00000248960
19	lnc-HMG20A-4	chr15:77960013-77960416	ENSG00000259281.1
20	lnc-HMG20A-3	chr15:77940435-77940672	NONHSAT047455
21	lnc-HMG20A-4	chr15:77960013-77960415	ENSG00000248960
22	lnc-HMG20A-3	chr15:77938700-77938853	ENSG00000259666.1
23	lnc-HMG20A-4	chr15:77959302-77959428	ENSG00000248960
24	lnc-HMG20A-4	chr15:77960013-77960533	NONHSAT047457
25	lnc-HMG20A-3	chr15:77934106-77934299	ENSG00000259666.1
26	lnc-HMG20A-2	chr15:77861312-77861518	ENSG00000259420.1
27	lnc-HMG20A-3	chr15:77940181-77941579	ENSG00000249469
28	lnc-HMG20A-4	chr15:77959302-77959428	ENSG00000259281.1
29	lnc-HMG20A-2	chr15:77864593-77864787	ENSG00000259420.1
30	lnc-HMG20A-3	chr15:77938730-77938853	ENSG00000259666.1
31	lnc-HMG20A-3	chr15:77934106-77934299	ENSG00000249469
32	lnc-HMG20A-2	chr15:77864907-77865206	ENSG00000259420.1
33	lnc-HMG20A-3	chr15:77943677-77944620	NONHSAT047452
34	lnc-HMG20A-3	chr15:77934106-77934299	NR_045123
35	lnc-HMG20A-3	chr15:77938730-77938853	NR_045123
36	lnc-HMG20A-3	chr15:77940181-77941581	NR_045123
37	lnc-HMG20A-2	chr15:77861312-77861518	ENSG00000259420.1
38	lnc-HMG20A-3	chr15:77940486-77940672	NONHSAT047452
39	lnc-HMG20A-3	chr15:77943677-77943997	ENSG00000259666.1

No data

Variant related genes	Relation type
ENSG00000259666	TF binding region
ENSG00000259420	TF binding region
LINGO1	TF binding region
ENSG00000259281	TF binding region
ENSG00000259666	CpG island
ENSG00000259420	CpG island
LINGO1	CpG island
ENSG00000259281	CpG island
ENSG00000259420	chromatin interactions
ENSG00000259281	chromatin interactions
ENSG00000169783	chromatin interactions
ENSG00000259666	chromatin interactions
ZNF594	miRNA target sites
DDX3X	miRNA target sites

Extended variants
information (count: 4894 )
Associated
traits (count: 53 )

Variant overlapped rSNPs/rCNVs (count:4894 , 50 per page) page: 1 2 3 4 5 6 7 ... 98

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12904553	chr15:77845959-77845960	Weak transcription Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs532674805	chr15:77845965-77845966	Weak transcription Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
3	rs548105569	chr15:77845971-77845972	Weak transcription Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
4	rs144718452	chr15:77846020-77846021	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
5	rs376418408	chr15:77846021-77846022	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
6	rs78021430	chr15:77846082-77846083	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
7	rs543354861	chr15:77846095-77846096	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
8	rs76439158	chr15:77846101-77846102	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
9	rs181862496	chr15:77846111-77846112	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
10	rs558469207	chr15:77846119-77846120	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
11	rs78874316	chr15:77846153-77846154	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
12	rs529500839	chr15:77846166-77846167	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
13	rs77653222	chr15:77846168-77846169	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
14	rs553206280	chr15:77846200-77846201	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs12905044	chr15:77846215-77846216	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
16	rs117256937	chr15:77846234-77846235	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs2458034	chr15:77846243-77846244	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs185200120	chr15:77846292-77846293	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs575410443	chr15:77846304-77846305	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs545944426	chr15:77846308-77846309	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs565323006	chr15:77846350-77846351	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs545319863	chr15:77846371-77846372	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs532703355	chr15:77846403-77846404	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs371001157	chr15:77846431-77846432	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs375833230	chr15:77846441-77846442	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs532911880	chr15:77846479-77846480	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs559947078	chr15:77846486-77846487	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs565356340	chr15:77846487-77846488	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs78942757	chr15:77846646-77846647	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
30	rs146691740	chr15:77846713-77846714	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
31	rs569761005	chr15:77846723-77846724	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
32	rs111683538	chr15:77846741-77846742	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
33	rs527383059	chr15:77846754-77846755	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
34	rs75103337	chr15:77846771-77846772	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
35	rs76959192	chr15:77846785-77846786	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
36	rs534770492	chr15:77846790-77846791	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
37	rs531332518	chr15:77846832-77846833	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
38	rs368261638	chr15:77846861-77846862	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
39	rs115359932	chr15:77846863-77846864	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
40	rs568353854	chr15:77846865-77846866	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
41	rs140303628	chr15:77846900-77846901	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
42	rs114292935	chr15:77846901-77846902	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
43	rs567413959	chr15:77846910-77846911	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
44	rs114685729	chr15:77846980-77846981	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
45	rs377082254	chr15:77847090-77847091	Weak transcription Enhancers Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs150338092	chr15:77847098-77847099	Weak transcription Enhancers Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs189671049	chr15:77847113-77847114	Weak transcription Enhancers Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs373755510	chr15:77847138-77847139	Weak transcription Enhancers Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs530325305	chr15:77847181-77847182	Weak transcription Enhancers Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs117216804	chr15:77847182-77847183	Weak transcription Enhancers Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:53)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	CNVD
Wilms tumour	21544195	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
Gastrointestinal stromal cancer	16982739	CNVD
Prostate cancer	18632612	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
Autism	17322880	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Lung cancer	18438408	CNVD
Myelofibrosis	22110671	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Papillary thyroid carcinoma	22161024	CNVD
Autism	21480499	CNVD
Breast cancer	17603634	CNVD
Acute myeloid leukemia	16864856	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:2479 , 50 per page) page: 1 2 3 4 5 6 7 ... 50

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:77836200-77846600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
2	chr15:77838600-77849800	Weak transcription	H9 Cell Line	embryonic stem cell
3	chr15:77838800-77849000	Weak transcription	Gastric	stomach
4	chr15:77839800-77846400	Weak transcription	Fetal Heart	heart
5	chr15:77840600-77848600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr15:77841400-77846600	Weak transcription	Cortex derived primary cultured neurospheres	brain
7	chr15:77841600-77846000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
8	chr15:77841600-77846800	Weak transcription	Spleen	Spleen
9	chr15:77841600-77847000	Weak transcription	Fetal Brain Female	brain
10	chr15:77841600-77849600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
11	chr15:77842200-77850200	Enhancers	Brain Inferior Temporal Lobe	brain
12	chr15:77842800-77850400	Enhancers	Brain Hippocampus Middle	brain
13	chr15:77843400-77846400	Weak transcription	Fetal Stomach	stomach
14	chr15:77843600-77846200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
15	chr15:77843800-77846000	Bivalent Enhancer	HepG2	liver
16	chr15:77843800-77847400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr15:77844000-77846000	Weak transcription	Fetal Muscle Leg	muscle
18	chr15:77844000-77846600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
19	chr15:77844400-77846600	Enhancers	HUES6 Cell Line	embryonic stem cell
20	chr15:77844400-77848400	Weak transcription	Fetal Intestine Small	intestine
21	chr15:77844400-77850200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
22	chr15:77844600-77850000	Enhancers	Brain Anterior Caudate	brain
23	chr15:77844800-77848200	Enhancers	Brain Angular Gyrus	brain
24	chr15:77844800-77849800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
25	chr15:77844800-77849800	Enhancers	Brain Substantia Nigra	brain
26	chr15:77845000-77849400	Weak transcription	Duodenum Mucosa	Duodenum
27	chr15:77845200-77846200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
28	chr15:77845200-77846200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
29	chr15:77845200-77846200	Weak transcription	Brain Cingulate Gyrus	brain
30	chr15:77845400-77846200	Enhancers	Fetal Brain Male	brain
31	chr15:77845400-77846600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
32	chr15:77845600-77847200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr15:77845800-77846000	Flanking Bivalent TSS/Enh	H1 Derived Mesenchymal Stem Cells	ES cell derived
34	chr15:77845800-77846000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
35	chr15:77846000-77846200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
36	chr15:77846000-77846200	Enhancers	GM12878-XiMat	blood
37	chr15:77846000-77846200	Enhancers	HepG2	liver
38	chr15:77846000-77846600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
39	chr15:77846000-77847800	Enhancers	Fetal Muscle Leg	muscle
40	chr15:77846000-77848800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
41	chr15:77846200-77846400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
42	chr15:77846200-77846400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
43	chr15:77846200-77846600	Weak transcription	Fetal Brain Male	brain
44	chr15:77846200-77846600	Flanking Active TSS	HepG2	liver
45	chr15:77846200-77847000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
46	chr15:77846200-77848000	Bivalent Enhancer	Placenta	Placenta
47	chr15:77846200-77850200	Enhancers	Brain Cingulate Gyrus	brain
48	chr15:77846400-77846800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
49	chr15:77846400-77846800	Enhancers	Brain Germinal Matrix	brain
50	chr15:77846400-77847000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell

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