Variant report

Variant	nsv569992
Chromosome Location	chr15:75132319-75137868
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:911)
CpG islands
(count:549)
Chromatin interactive
region (count:46)
LncRNA
region (count:0)
Mature miRNA
region (count: 2)
miRNA target
sites (count:2)

(count:911 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:75135460-75135712	K562	blood:	n/a	n/a
2	ARID3A	chr15:75135518-75135625	HepG2	liver:	n/a	n/a
3	ATF2	chr15:75135341-75135964	GM12878	blood:	n/a	n/a
4	ATF2	chr15:75134884-75135478	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr15:75135466-75135862	GM12878	blood:	n/a	n/a
6	ATF3	chr15:75135405-75135840	GM12878	blood:	n/a	chr15:75135497-75135505 chr15:75135776-75135785 chr15:75135507-75135516
7	ATF3	chr15:75135426-75135883	K562	blood:	n/a	chr15:75135497-75135505 chr15:75135776-75135785 chr15:75135507-75135516
8	ATF3	chr15:75135506-75135787	H1-hESC	embryonic stem cell:	n/a	chr15:75135776-75135785 chr15:75135507-75135516
9	ATF3	chr15:75135541-75135789	GM12878	blood:	n/a	chr15:75135776-75135785
10	ATF3	chr15:75135459-75135846	H1-hESC	embryonic stem cell:	n/a	chr15:75135497-75135505 chr15:75135776-75135785 chr15:75135507-75135516
11	BACH1	chr15:75135000-75135200	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr15:75135491-75135927	H1-hESC	embryonic stem cell:	n/a	n/a
13	BCL3	chr15:75135238-75135906	GM12878	blood:	n/a	chr15:75135784-75135793 chr15:75135479-75135492 chr15:75135594-75135607
14	BCL3	chr15:75135032-75135945	GM12878	blood:	n/a	chr15:75135784-75135793 chr15:75135479-75135492 chr15:75135594-75135607
15	BCL3	chr15:75135070-75135908	A549	lung:	n/a	chr15:75135784-75135793 chr15:75135479-75135492 chr15:75135594-75135607
16	BCL3	chr15:75134860-75135950	A549	lung:	n/a	chr15:75135784-75135793 chr15:75135479-75135492 chr15:75135594-75135607
17	BCLAF1	chr15:75134951-75136031	GM12878	blood:	n/a	chr15:75135784-75135793 chr15:75135479-75135492 chr15:75135594-75135607
18	BCLAF1	chr15:75134960-75135941	GM12878	blood:	n/a	chr15:75135784-75135793 chr15:75135479-75135492 chr15:75135594-75135607
19	BHLHE40	chr15:75135008-75135988	K562	blood:	n/a	chr15:75135287-75135303
20	BHLHE40	chr15:75135526-75135808	A549	lung:	n/a	n/a
21	BHLHE40	chr15:75135435-75135931	HepG2	liver:	n/a	n/a
22	BHLHE40	chr15:75135297-75136030	GM12878	blood:	n/a	n/a
23	BRCA1	chr15:75135628-75135795	GM12878	blood:	n/a	n/a
24	BRCA1	chr15:75135630-75135635	Hela-S3	cervix:	n/a	n/a
25	BRCA1	chr15:75135196-75135236	Hela-S3	cervix:	n/a	n/a
26	BRCA1	chr15:75135515-75135708	HepG2	liver:	n/a	n/a
27	BRCA1	chr15:75135625-75135787	H1-hESC	embryonic stem cell:	n/a	n/a
28	CBX3	chr15:75135439-75135874	K562	blood:	n/a	n/a
29	CCNT2	chr15:75135154-75135958	K562	blood:	n/a	chr15:75135606-75135615
30	CEBPB	chr15:75135339-75135638	Hela-S3	cervix:	n/a	n/a
31	CEBPD	chr15:75135320-75135644	HepG2	liver:	n/a	n/a
32	CEBPD	chr15:75135288-75135731	HepG2	liver:	n/a	n/a
33	CHD1	chr15:75134911-75135365	H1-hESC	embryonic stem cell:	n/a	chr15:75135224-75135234
34	CHD1	chr15:75135073-75135704	GM12878	blood:	n/a	chr15:75135224-75135234 chr15:75135508-75135518
35	CHD2	chr15:75135516-75135881	H1-hESC	embryonic stem cell:	n/a	n/a
36	CHD2	chr15:75135530-75135803	HepG2	liver:	n/a	n/a
37	CHD2	chr15:75135282-75135920	GM12878	blood:	n/a	chr15:75135885-75135892 chr15:75135508-75135518
38	CHD2	chr15:75134966-75135232	H1-hESC	embryonic stem cell:	n/a	n/a
39	CHD2	chr15:75135032-75135992	K562	blood:	n/a	chr15:75135885-75135892 chr15:75135224-75135234 chr15:75135508-75135518
40	CHD2	chr15:75134947-75135147	Hela-S3	cervix:	n/a	n/a
41	CHD2	chr15:75135358-75135929	Hela-S3	cervix:	n/a	chr15:75135885-75135892 chr15:75135508-75135518
42	CREB1	chr15:75135297-75136022	GM12878	blood:	n/a	n/a
43	CREB1	chr15:75135368-75135784	A549	lung:	n/a	n/a
44	CREB1	chr15:75135303-75135897	K562	blood:	n/a	n/a
45	CREB1	chr15:75135165-75135906	A549	lung:	n/a	n/a
46	CREB1	chr15:75134888-75135872	H1-hESC	embryonic stem cell:	n/a	n/a
47	CTBP2	chr15:75134881-75135611	H1-hESC	embryonic stem cell:	n/a	n/a
48	CTCF	chr15:75135040-75135190	HepG2	liver:	n/a	chr15:75135149-75135157
49	CTCF	chr15:75132444-75132645	K562	blood:	n/a	chr15:75132535-75132553 chr15:75132537-75132550
50	CTCF	chr15:75132540-75132690	HCM	heart:	n/a	n/a

(count:549 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:75135169-75135219	CMK	blood:	n/a
2	chr15:75135169-75135219	NT2-D1	testis:	n/a
3	chr15:75135746-75135796	AG09319	gingival:	n/a
4	chr15:75135187-75135237	PFSK-1	brain:	n/a
5	chr15:75132713-75132763	A549	lung:	n/a
6	chr15:75135187-75135237	GM19239	blood:	n/a
7	chr15:75136007-75136057	Jurkat	blood:	n/a
8	chr15:75135187-75135237	LNCaP	prostate:	n/a
9	chr15:75135169-75135219	HRPEpiC	eye:	n/a
10	chr15:75135717-75135767	HMEC	breast:	n/a
11	chr15:75136278-75136328	CMK	blood:	n/a
12	chr15:75135717-75135767	ECC-1	luminal epithelium:	n/a
13	chr15:75135746-75135796	PFSK-1	brain:	n/a
14	chr15:75135169-75135219	GM12878	blood:	n/a
15	chr15:75136278-75136328	HUVEC	blood vessel:	n/a
16	chr15:75136278-75136328	Caco-2	colon:	n/a
17	chr15:75135266-75135316	HIPEpiC	eye:	n/a
18	chr15:75132713-75132763	BJ	skin:	n/a
19	chr15:75135187-75135237	PANC-1	pancreas:	n/a
20	chr15:75135266-75135316	HCM	heart:	n/a
21	chr15:75135746-75135796	K562	blood:	n/a
22	chr15:75136278-75136328	HNPCEpiC	eye:	n/a
23	chr15:75132713-75132763	SK-N-SH_RA	brain:	n/a
24	chr15:75135717-75135767	AG09319	gingival:	n/a
25	chr15:75136007-75136057	HL-60	blood:	n/a
26	chr15:75135266-75135316	HRCEpiC	kidney:	n/a
27	chr15:75136278-75136328	U87	brain:	n/a
28	chr15:75135746-75135796	CMK	blood:	n/a
29	chr15:75135169-75135219	HCPEpiC	choroid plexus:	n/a
30	chr15:75135169-75135219	MCF-7	breast:	n/a
31	chr15:75135746-75135796	Hela-S3	cervix:	n/a
32	chr15:75135266-75135316	HL-60	blood:	n/a
33	chr15:75135746-75135796	NT2-D1	testis:	n/a
34	chr15:75135169-75135219	HL-60	blood:	n/a
35	chr15:75135746-75135796	SAEC	small airway:	n/a
36	chr15:75136278-75136328	ProgFib	skin:	n/a
37	chr15:75132713-75132763	PANC-1	pancreas:	n/a
38	chr15:75132713-75132763	AG04450	lung:	fetal
39	chr15:75135169-75135219	AG09319	gingival:	n/a
40	chr15:75135815-75135865	H1-hESC	embryonic stem cell:	embryo
41	chr15:75136007-75136057	GM12878	blood:	n/a
42	chr15:75135187-75135237	Hela-S3	cervix:	n/a
43	chr15:75132713-75132763	HL-60	blood:	n/a
44	chr15:75135266-75135316	AG04450	lung:	fetal
45	chr15:75135717-75135767	IMR90	lung:	fetal
46	chr15:75135187-75135237	A549	lung:	n/a
47	chr15:75136007-75136057	HPAEpiC	pulmonary alveolar:	n/a
48	chr15:75132713-75132763	AG09309	skin:	n/a
49	chr15:75136278-75136328	HCPEpiC	choroid plexus:	n/a
50	chr15:75135815-75135865	MCF-7	breast:	n/a

(count:46 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:75115272..75120114-chr15:75130983..75135707,7	K562	blood:
2	chr15:75132063..75136088-chr15:75165447..75167881,5	K562	blood:
3	chr15:75133683..75136875-chr15:75181140..75184004,7	K562	blood:
4	chr15:74926089..74928915-chr15:75133890..75136502,2	MCF-7	breast:
5	chr15:75131716..75139878-chr15:75227772..75233177,11	MCF-7	breast:
6	chr15:75134051..75136456-chr15:75197581..75199707,3	K562	blood:
7	chr15:75090900..75093717-chr15:75134239..75137508,3	MCF-7	breast:
8	chr15:75134593..75136676-chr15:75247766..75251919,4	MCF-7	breast:
9	chr15:75118538..75120714-chr15:75135771..75139266,4	K562	blood:
10	chr15:74906653..74908395-chr15:75135147..75137390,2	K562	blood:
11	chr15:75132595..75137581-chr15:75190842..75194074,4	K562	blood:
12	chr15:75129767..75136088-chr15:75163908..75167881,8	K562	blood:
13	chr15:75135967..75138215-chr15:75196939..75199387,3	K562	blood:
14	chr15:75135336..75137971-chr15:75192308..75194100,2	MCF-7	breast:
15	chr15:75079215..75085047-chr15:75133215..75137478,7	MCF-7	breast:
16	chr11:65190032..65190914-chr15:75134891..75135778,2	Hela-S3	cervix:
17	chr15:75135797..75138668-chr15:75143176..75146551,4	K562	blood:
18	chr15:75052835..75054344-chr15:75136259..75138062,2	K562	blood:
19	chr15:75135427..75140750-chr15:75141950..75147054,10	K562	blood:
20	chr15:75072228..75074857-chr15:75134119..75137193,5	K562	blood:
21	chr15:75133947..75135664-chr15:75246136..75249268,3	MCF-7	breast:
22	chr15:75133989..75136127-chr15:75187296..75189781,2	K562	blood:
23	chr15:74832995..74834922-chr15:75133837..75135469,2	K562	blood:
24	chr15:75133950..75137156-chr15:75180779..75184661,9	MCF-7	breast:
25	chr15:75073376..75079113-chr15:75130007..75137097,15	MCF-7	breast:
26	chr15:75083424..75086045-chr15:75130919..75133658,2	K562	blood:
27	chr15:75134990..75135563-chr20:30194262..30195030,2	Hela-S3	cervix:
28	chr15:75136180..75138079-chr15:75161900..75164141,2	K562	blood:
29	chr15:75106165..75113668-chr15:75132311..75136608,10	MCF-7	breast:
30	chr15:75135715..75138276-chr15:75139819..75143025,6	K562	blood:
31	chr15:75133790..75137554-chr15:75195204..75200578,14	MCF-7	breast:
32	chr15:75133406..75136691-chr15:75228046..75231533,6	MCF-7	breast:
33	chr15:75073852..75074625-chr15:75135150..75135967,3	MCF-7	breast:
34	chr15:75090773..75092693-chr15:75133525..75135797,3	K562	blood:
35	chr15:75063457..75064044-chr15:75132063..75132629,2	K562	blood:
36	chr15:75134049..75139648-chr15:75161531..75167020,13	MCF-7	breast:
37	chr15:75135788..75137937-chr15:75174373..75175874,2	MCF-7	breast:
38	chr15:75072623..75074857-chr15:75134348..75137142,2	K562	blood:
39	chr15:75105168..75109047-chr15:75134120..75137766,4	K562	blood:
40	chr15:74906299..74909390-chr15:75133726..75137690,7	MCF-7	breast:
41	chr15:75091193..75092930-chr15:75133955..75135797,2	K562	blood:
42	chr15:75132852..75135633-chr15:75196341..75200571,3	K562	blood:
43	chr15:75134794..75137581-chr15:75190842..75193156,3	K562	blood:
44	chr15:45459092..45459965-chr15:75134556..75135332,2	Hela-S3	cervix:
45	chr15:75134997..75135662-chr6:108279356..108279933,2	HCT-116	colon:
46	chr15:75131329..75142649-chr15:75180088..75200119,60	MCF-7	breast:

No data

miRNA name	Chromosome Location	mirBase accession
hsa-miR-6882-5p	chr15:75133022-75133043	MIMAT0027664
hsa-miR-6882-3p	chr15:75132983-75133006	MIMAT0027665

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	SCAMP2	hsa-miR-124-3p	chr15:75137352-75137371
2	SCAMP2	hsa-miR-124-3p	chr15:75137358-75137351

Variant related genes	Relation type
ULK3	TF binding region
ULK3	CpG island
ENSG00000261606	chromatin interactions
ENSG00000178802	chromatin interactions
ENSG00000140497	chromatin interactions
ENSG00000178741	chromatin interactions
ENSG00000264395	chromatin interactions
ENSG00000178718	chromatin interactions
ENSG00000260824	chromatin interactions
ENSG00000179151	chromatin interactions
ENSG00000264386	chromatin interactions
ENSG00000245532	chromatin interactions
ENSG00000213578	chromatin interactions
ENSG00000198794	chromatin interactions
ENSG00000179335	chromatin interactions
ENSG00000140506	chromatin interactions
ENSG00000179361	chromatin interactions
ENSG00000178761	chromatin interactions
ENSG00000259539	chromatin interactions
ENSG00000260919	chromatin interactions
ENSG00000025796	chromatin interactions
ENSG00000103653	chromatin interactions

Extended variants
information (count: 211 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:211 , 50 per page) page: 1 2 3 4 5

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs936229	chr15:75132319-75132320	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	10 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance disease
2	rs537616341	chr15:75132330-75132331	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
3	rs62006630	chr15:75132355-75132356	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
4	rs558906987	chr15:75132361-75132362	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
5	rs576878248	chr15:75132430-75132431	Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
6	rs541136619	chr15:75132432-75132433	Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
7	rs140140963	chr15:75132468-75132469	Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
8	rs574537448	chr15:75132470-75132471	Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
9	rs72730515	chr15:75132481-75132482	Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	10 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs143508097	chr15:75132486-75132487	Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
11	rs561268142	chr15:75132488-75132489	Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
12	rs12908814	chr15:75132490-75132491	Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	10 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
13	rs191110654	chr15:75132505-75132506	Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
14	rs565078811	chr15:75132517-75132518	Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
15	rs113546085	chr15:75132520-75132521	Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
16	rs532207597	chr15:75132542-75132543	Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
17	rs368958635	chr15:75132594-75132595	Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
18	rs373403457	chr15:75132602-75132603	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
19	rs200910015	chr15:75132634-75132635	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
20	rs374894669	chr15:75132640-75132641	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
21	rs565677369	chr15:75132647-75132648	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
22	rs369535106	chr15:75132681-75132682	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
23	rs529723609	chr15:75132726-75132727	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region CpG island Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
24	rs375102737	chr15:75132766-75132767	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
25	rs373004411	chr15:75132816-75132817	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
26	rs62006631	chr15:75132820-75132821	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
27	rs182854590	chr15:75132831-75132832	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
28	rs376196727	chr15:75132833-75132834	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
29	rs373362531	chr15:75132846-75132847	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
30	rs377064776	chr15:75132875-75132876	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
31	rs370092870	chr15:75132879-75132880	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
32	rs375326807	chr15:75132890-75132891	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
33	rs201787599	chr15:75132892-75132893	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
34	rs35249396	chr15:75132921-75132922	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
35	rs370621400	chr15:75132935-75132936	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
36	rs375863086	chr15:75132954-75132955	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
37	rs368307518	chr15:75132955-75132956	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
38	rs372901201	chr15:75132972-75132973	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
39	rs531063819	chr15:75132986-75132987	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region miRNA	10 gene(s)	Overlapped CNVs	n/a
40	rs201019781	chr15:75132996-75132997	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region miRNA	10 gene(s)	Overlapped CNVs	n/a
41	rs532898162	chr15:75133002-75133003	Weak transcription Strong transcription Genic enhancers Active TSS Enhancers	TF binding region Chromatin interactive region miRNA	10 gene(s)	Overlapped CNVs	n/a
42	rs371263425	chr15:75133016-75133017	Weak transcription Strong transcription Genic enhancers Active TSS Enhancers	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
43	rs557100251	chr15:75133118-75133119	Weak transcription Strong transcription Genic enhancers Active TSS Enhancers	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
44	rs372908711	chr15:75133150-75133151	Weak transcription Strong transcription Genic enhancers Active TSS Enhancers	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
45	rs576240887	chr15:75133195-75133196	Weak transcription Strong transcription Genic enhancers Active TSS Enhancers	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
46	rs881536	chr15:75133220-75133221	Strong transcription Weak transcription Genic enhancers Enhancers Active TSS	TF binding region Chromatin interactive region	11 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
47	rs565064302	chr15:75133373-75133374	Strong transcription Weak transcription Genic enhancers Enhancers Active TSS	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
48	rs532397618	chr15:75133400-75133401	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Active TSS	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
49	rs562956771	chr15:75133548-75133549	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Active TSS	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
50	rs541108492	chr15:75133556-75133557	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Active TSS	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:68)

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
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
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
Breast cancer	21364760	CNVD
Epilepsy	22083797	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Myelofibrosis	22110671	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Pancreatic cancer	17952125	CNVD
Lung cancer	18438408	CNVD

Chromatin state (count:949 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:75121400-75134600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr15:75121800-75134600	Weak transcription	Pancreatic Islets	Pancreatic Islet
3	chr15:75123800-75134200	Weak transcription	HUES64 Cell Line	embryonic stem cell
4	chr15:75123800-75134200	Weak transcription	Primary B cells from cord blood	blood
5	chr15:75123800-75134400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
6	chr15:75123800-75134400	Weak transcription	Muscle Satellite Cultured Cells	--
7	chr15:75123800-75134400	Weak transcription	HSMM	muscle
8	chr15:75124000-75134400	Weak transcription	HSMMtube	muscle
9	chr15:75124400-75134400	Weak transcription	Fetal Lung	lung
10	chr15:75124800-75134400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
11	chr15:75124800-75134400	Weak transcription	Psoas Muscle	Psoas
12	chr15:75125000-75134000	Weak transcription	Stomach Mucosa	stomach
13	chr15:75125000-75134600	Weak transcription	H9 Cell Line	embryonic stem cell
14	chr15:75125200-75134800	Weak transcription	Aorta	Aorta
15	chr15:75126200-75132800	Weak transcription	Hela-S3	cervix
16	chr15:75126200-75134400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr15:75126400-75132800	Weak transcription	Primary hematopoietic stem cells	blood
18	chr15:75126600-75134200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr15:75126600-75134400	Weak transcription	GM12878-XiMat	blood
20	chr15:75126800-75134600	Weak transcription	Placenta Amnion	Placenta Amnion
21	chr15:75127200-75133400	Strong transcription	Primary hematopoietic stem cells short term culture	blood
22	chr15:75127600-75132400	Strong transcription	Fetal Brain Female	brain
23	chr15:75127600-75133600	Strong transcription	Brain Germinal Matrix	brain
24	chr15:75127800-75132800	Strong transcription	Fetal Muscle Trunk	muscle
25	chr15:75127800-75132800	Strong transcription	Right Ventricle	heart
26	chr15:75127800-75133000	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
27	chr15:75127800-75133000	Strong transcription	Fetal Muscle Leg	muscle
28	chr15:75127800-75133000	Strong transcription	Pancreas	Pancrea
29	chr15:75127800-75133400	Strong transcription	Cortex derived primary cultured neurospheres	brain
30	chr15:75127800-75133800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
31	chr15:75127800-75133800	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
32	chr15:75127800-75133800	Strong transcription	Fetal Stomach	stomach
33	chr15:75128000-75132400	Strong transcription	Brain Hippocampus Middle	brain
34	chr15:75128000-75132400	Strong transcription	Fetal Intestine Large	intestine
35	chr15:75128000-75132800	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
36	chr15:75128000-75132800	Strong transcription	Brain Cingulate Gyrus	brain
37	chr15:75128000-75133000	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
38	chr15:75128000-75133000	Strong transcription	Skeletal Muscle Male	skeletal muscle
39	chr15:75128000-75133400	Strong transcription	Primary T helper cells PMA-I stimulated	--
40	chr15:75128000-75133400	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
41	chr15:75128000-75133400	Strong transcription	Brain Anterior Caudate	brain
42	chr15:75128000-75133400	Strong transcription	Gastric	stomach
43	chr15:75128000-75133400	Strong transcription	Lung	lung
44	chr15:75128000-75133400	Strong transcription	Rectal Mucosa Donor 29	rectum
45	chr15:75128000-75133400	Strong transcription	Sigmoid Colon	Sigmoid Colon
46	chr15:75128000-75133400	Strong transcription	Spleen	Spleen
47	chr15:75128000-75133600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
48	chr15:75128000-75133600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
49	chr15:75128000-75133600	Strong transcription	Placenta	Placenta
50	chr15:75128000-75133800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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