Variant report

Variant	nsv498847
Chromosome Location	chr15:56667038-56896395
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1354)
CpG islands
(count:916)
Chromatin interactive
region (count:47)
LncRNA
region (count:13)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1354 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:56721089-56721405	K562	blood:	n/a	n/a
2	ARID3A	chr15:56757183-56757342	HepG2	liver:	n/a	n/a
3	ARID3A	chr15:56788752-56789118	HepG2	liver:	n/a	chr15:56788814-56788830
4	ARID3A	chr15:56881619-56881703	K562	blood:	n/a	n/a
5	ARID3A	chr15:56788756-56789177	K562	blood:	n/a	chr15:56788814-56788830
6	ARID3A	chr15:56757439-56757589	K562	blood:	n/a	n/a
7	ATF1	chr15:56761692-56762037	K562	blood:	n/a	n/a
8	ATF1	chr15:56701414-56701616	K562	blood:	n/a	n/a
9	ATF1	chr15:56785297-56785306	K562	blood:	n/a	n/a
10	ATF2	chr15:56757025-56757555	GM12878	blood:	n/a	n/a
11	ATF3	chr15:56767569-56767875	K562	blood:	n/a	n/a
12	BACH1	chr15:56757918-56757978	K562	blood:	n/a	n/a
13	BACH1	chr15:56757137-56757703	H1-hESC	embryonic stem cell:	n/a	n/a
14	BATF	chr15:56788822-56789212	GM12878	blood:	n/a	n/a
15	BCL3	chr15:56757103-56757795	A549	lung:	n/a	n/a
16	BCL3	chr15:56757037-56757647	GM12878	blood:	n/a	n/a
17	BCLAF1	chr15:56757083-56757625	GM12878	blood:	n/a	n/a
18	BHLHE40	chr15:56830099-56830356	GM12878	blood:	n/a	n/a
19	BHLHE40	chr15:56704886-56704981	GM12878	blood:	n/a	n/a
20	BHLHE40	chr15:56757494-56757730	HepG2	liver:	n/a	n/a
21	BHLHE40	chr15:56757184-56757611	K562	blood:	n/a	chr15:56757254-56757270
22	BHLHE40	chr15:56783358-56783670	GM12878	blood:	n/a	n/a
23	BHLHE40	chr15:56844843-56845124	K562	blood:	n/a	n/a
24	CBX3	chr15:56878477-56878666	K562	blood:	n/a	n/a
25	CBX3	chr15:56878445-56878784	K562	blood:	n/a	n/a
26	CBX3	chr15:56878353-56878826	HCT-116	colon:	n/a	n/a
27	CBX3	chr15:56757101-56757760	K562	blood:	n/a	n/a
28	CBX3	chr15:56757309-56757702	K562	blood:	n/a	n/a
29	CCNT2	chr15:56757151-56757524	K562	blood:	n/a	n/a
30	CEBPB	chr15:56767633-56767903	HepG2	liver:	n/a	chr15:56767741-56767752
31	CEBPB	chr15:56724457-56724851	A549	lung:	n/a	chr15:56724724-56724735
32	CEBPB	chr15:56788854-56789190	IMR90	lung:	n/a	n/a
33	CEBPB	chr15:56848658-56849122	A549	lung:	n/a	chr15:56848952-56848963
34	CEBPB	chr15:56715699-56715899	IMR90	lung:	n/a	n/a
35	CEBPB	chr15:56788871-56789188	K562	blood:	n/a	n/a
36	CEBPB	chr15:56724449-56724866	HepG2	liver:	n/a	chr15:56724724-56724735
37	CEBPB	chr15:56845045-56845245	A549	lung:	n/a	n/a
38	CEBPB	chr15:56854327-56854483	HepG2	liver:	n/a	chr15:56854398-56854409
39	CEBPB	chr15:56748579-56748651	A549	lung:	n/a	n/a
40	CEBPB	chr15:56724404-56724778	IMR90	lung:	n/a	chr15:56724724-56724735
41	CEBPB	chr15:56715740-56715857	A549	lung:	n/a	n/a
42	CEBPB	chr15:56788802-56789166	H1-hESC	embryonic stem cell:	n/a	n/a
43	CEBPB	chr15:56767580-56767912	IMR90	lung:	n/a	chr15:56767741-56767752
44	CEBPB	chr15:56767650-56767857	H1-hESC	embryonic stem cell:	n/a	chr15:56767741-56767752
45	CEBPB	chr15:56848852-56849052	K562	blood:	n/a	chr15:56848952-56848963
46	CEBPB	chr15:56848686-56849125	IMR90	lung:	n/a	chr15:56848952-56848963
47	CEBPB	chr15:56828054-56828116	K562	blood:	n/a	n/a
48	CEBPB	chr15:56757311-56757566	K562	blood:	n/a	n/a
49	CEBPB	chr15:56767644-56767889	Hela-S3	cervix:	n/a	chr15:56767741-56767752
50	CEBPB	chr15:56854262-56854583	HepG2	liver:	n/a	chr15:56854398-56854409

(count:916 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:56757499-56757549	AG10803	skin:	n/a
2	chr15:56757499-56757549	AG10803	skin:	n/a
3	chr15:56725876-56725926	HCPEpiC	choroid plexus:	n/a
4	chr15:56757290-56757340	HNPCEpiC	eye:	n/a
5	chr15:56725876-56725926	HRE	kidney:	n/a
6	chr15:56757314-56757364	PANC-1	pancreas:	n/a
7	chr15:56757517-56757567	T-47D	breast:	n/a
8	chr15:56759655-56759705	HRCEpiC	kidney:	n/a
9	chr15:56757806-56757856	PFSK-1	brain:	n/a
10	chr15:56757806-56757856	AG04449	skin:	fetal
11	chr15:56725876-56725926	ProgFib	skin:	n/a
12	chr15:56757180-56757230	AoSMC	blood vessel:	n/a
13	chr15:56757180-56757230	GM12892	blood:	n/a
14	chr15:56757806-56757856	HIPEpiC	eye:	n/a
15	chr15:56757108-56757158	SK-N-SH_RA	brain:	n/a
16	chr15:56758270-56758320	HAEpiC	amniotic membrane:	n/a
17	chr15:56757108-56757158	SK-N-MC	brain:	n/a
18	chr15:56757180-56757230	HRPEpiC	eye:	n/a
19	chr15:56757499-56757549	GM12878	blood:	n/a
20	chr15:56757290-56757340	NH-A	brain:	n/a
21	chr15:56757806-56757856	MCF10A-Er-Src	breast:	n/a
22	chr15:56759655-56759705	GM19239	blood:	n/a
23	chr15:56757517-56757567	HRE	kidney:	n/a
24	chr15:56757108-56757158	SK-N-SH	brain:	n/a
25	chr15:56725876-56725926	HMEC	breast:	n/a
26	chr15:56757312-56757362	MCF10A-Er-Src	breast:	n/a
27	chr15:56757108-56757158	MCF-7	breast:	n/a
28	chr15:56757314-56757364	RPTEC	kidney:	n/a
29	chr15:56757806-56757856	CMK	blood:	n/a
30	chr15:56757499-56757549	AG04449	skin:	fetal
31	chr15:56757625-56757675	ovcar-3	ovarian:	n/a
32	chr15:56757290-56757340	Hela-S3	cervix:	n/a
33	chr15:56757314-56757364	NB4	blood:	n/a
34	chr15:56757325-56757375	Caco-2	colon:	n/a
35	chr15:56757499-56757549	LNCaP	prostate:	n/a
36	chr15:56757314-56757364	NHDF-neo	bronchial:	n/a
37	chr15:56758270-56758320	NHDF-neo	bronchial:	n/a
38	chr15:56757499-56757549	HCT-116	colon:	n/a
39	chr15:56725876-56725926	HUVEC	blood vessel:	n/a
40	chr15:56757625-56757675	GM12892	blood:	n/a
41	chr15:56757108-56757158	SAEC	small airway:	n/a
42	chr15:56757314-56757364	Caco-2	colon:	n/a
43	chr15:56759655-56759705	H1-hESC	embryonic stem cell:	embryo
44	chr15:56758270-56758320	T-47D	breast:	n/a
45	chr15:56757312-56757362	MCF-7	breast:	n/a
46	chr15:56725876-56725926	HIPEpiC	eye:	n/a
47	chr15:56757314-56757364	SAEC	small airway:	n/a
48	chr15:56757290-56757340	HRE	kidney:	n/a
49	chr15:56759655-56759705	GM12892	blood:	n/a
50	chr15:56757325-56757375	NB4	blood:	n/a

(count:47 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:56814069..56816681-chr15:56818491..56820321,2	K562	blood:
2	chr15:56811740..56813746-chr15:56822934..56825907,2	K562	blood:
3	chr15:56783040..56784156-chr15:57161563..57162645,6	K562	blood:
4	chr15:56540398..56542023-chr15:56720800..56721752,16	MCF-7	breast:
5	chr15:56697956..56699869-chr15:56701440..56703984,2	MCF-7	breast:
6	chr15:56541018..56541999-chr15:56720733..56721455,3	MCF-7	breast:
7	chr15:56756734..56759056-chr15:56761429..56763544,2	K562	blood:
8	chr15:56662303..56664925-chr15:56669257..56671232,2	MCF-7	breast:
9	chr15:56788851..56789408-chr15:57103635..57104349,2	MCF-7	breast:
10	chr15:56066629..56067204-chr15:56720771..56721659,2	K562	blood:
11	chr15:56791160..56793250-chr15:56794933..56796796,2	K562	blood:
12	chr15:56541012..56541917-chr15:56720826..56721341,2	K562	blood:
13	chr15:56731142..56732969-chr15:56736651..56738760,2	K562	blood:
14	chr15:56782685..56785505-chr15:57019755..57021681,2	K562	blood:
15	chr15:56537725..56539025-chr15:56720287..56722326,16	MCF-7	breast:
16	chr15:56787707..56790107-chr15:57597582..57600140,2	MCF-7	breast:
17	chr15:56817798..56822839-chr15:56825097..56828742,5	K562	blood:
18	chr15:56788702..56789394-chr15:57161523..57162414,2	MCF-7	breast:
19	chr15:56536734..56539507-chr15:56718886..56721172,2	MCF-7	breast:
20	chr15:56811740..56813746-chr15:56822934..56825907,2	K562	blood:
21	chr15:56775436..56776246-chr15:56784313..56784975,2	K562	blood:
22	chr15:56775436..56776246-chr15:56784313..56784975,2	K562	blood:
23	chr15:56788456..56789162-chr15:57113822..57114589,2	MCF-7	breast:
24	chr15:56817798..56822286-chr15:56825097..56828742,4	K562	blood:
25	chr15:56814069..56816681-chr15:56818491..56820321,2	K562	blood:
26	chr15:56762921..56765735-chr15:56765770..56767934,2	K562	blood:
27	chr15:55940442..55941185-chr15:56720975..56721740,2	K562	blood:
28	chr15:56817798..56822286-chr15:56825097..56828742,4	K562	blood:
29	chr15:56714747..56716284-chr15:56716589..56718483,2	MCF-7	breast:
30	chr15:56762921..56765735-chr15:56765770..56767934,2	K562	blood:
31	chr15:56788753..56789362-chr15:57161247..57161954,2	K562	blood:
32	chr15:56788444..56789415-chr15:57598413..57599206,3	K562	blood:
33	chr15:56536083..56538918-chr15:56762516..56765231,2	K562	blood:
34	chr15:56587524..56588313-chr15:56720286..56721333,4	MCF-7	breast:
35	chr15:56788688..56789403-chr15:57430424..57431057,2	MCF-7	breast:
36	chr15:56696715..56699099-chr15:56700955..56702991,2	MCF-7	breast:
37	chr15:56537986..56539019-chr15:56720847..56721772,4	K562	blood:
38	chr15:56782970..56783589-chr15:57598753..57599463,2	MCF-7	breast:
39	chr15:56714747..56716284-chr15:56716589..56718483,2	MCF-7	breast:
40	chr15:56788863..56789371-chr16:34759996..34760825,2	MCF-7	breast:
41	chr15:56791160..56793250-chr15:56794933..56796796,2	K562	blood:
42	chr15:56773647..56776313-chr15:57177229..57179430,2	K562	blood:
43	chr15:56537987..56538847-chr15:56756234..56756979,2	MCF-7	breast:
44	chr15:56540966..56543133-chr15:56718827..56720916,2	MCF-7	breast:
45	chr15:56538080..56538849-chr15:56720711..56721356,4	MCF-7	breast:
46	chr15:56731142..56732969-chr15:56736651..56738760,2	K562	blood:
47	chr15:56817798..56822839-chr15:56825097..56828742,5	K562	blood:

(count:13 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF280D-1	chr15:56840136-56840205	ENSG00000260392.1
2	lnc-ZNF280D-1	chr15:56841355-56841708	ENSG00000260392.1
3	lnc-ZNF280D-1	chr15:56841355-56841708	ENSG00000260392.1
4	lnc-ZNF280D-1	chr15:56840645-56840799	ENSG00000260392.1
5	lnc-ZNF280D-2	chr15:56755978-56756445	NONHSAT044023
6	lnc-ZNF280D-1	chr15:56884918-56885050	ENSG00000260392.1
7	lnc-MNS1-1	chr15:56700681-56701128	ENSG00000261823.1
8	lnc-ZNF280D-1	chr15:56896038-56896069	ENSG00000260392.1
9	lnc-ZNF280D-1	chr15:56840058-56840205	ENSG00000260392.1
10	lnc-ZNF280D-1	chr15:56835757-56836010	ENSG00000260392.1
11	lnc-ZNF280D-2	chr15:56757168-56757283	NONHSAT044023
12	lnc-ZNF280D-1	chr15:56835150-56835294	ENSG00000260392.1
13	lnc-MNS1-1	chr15:56701994-56702384	ENSG00000261823.1

No data

Variant related genes	Relation type
ENSG00000259941	TF binding region
MNS1	TF binding region
TEX9	TF binding region
ENSG00000261823	TF binding region
ENSG00000259941	CpG island
MNS1	CpG island
TEX9	CpG island
ENSG00000261823	CpG island
ENSG00000151575	chromatin interactions
ENSG00000138587	chromatin interactions
ENSG00000261823	chromatin interactions

Extended variants
information (count: 7574 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:7574 , 50 per page) page: 1 2 3 4 5 6 7 ... 152

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs554614021	chr15:56667054-56667055	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs183190411	chr15:56667069-56667070	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs537276595	chr15:56667098-56667099	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs111735267	chr15:56667173-56667174	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs576765691	chr15:56667174-56667175	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs147306110	chr15:56667206-56667207	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs35357024	chr15:56667301-56667302	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs572076343	chr15:56667371-56667372	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs541014045	chr15:56667374-56667375	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs572368721	chr15:56667497-56667498	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs534968783	chr15:56667533-56667534	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs561464696	chr15:56667536-56667537	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs570583168	chr15:56667637-56667638	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs544035634	chr15:56667655-56667656	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs563692065	chr15:56667756-56667757	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs532859926	chr15:56667795-56667796	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs552874775	chr15:56667817-56667818	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs565693881	chr15:56667943-56667944	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs374126162	chr15:56668001-56668002	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs528125803	chr15:56668003-56668004	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs547855167	chr15:56668138-56668139	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs371221347	chr15:56668145-56668146	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs568191947	chr15:56668183-56668184	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs536736298	chr15:56668190-56668191	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs557127189	chr15:56668227-56668228	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs570263643	chr15:56668244-56668245	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs539366349	chr15:56668279-56668280	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs187774479	chr15:56668282-56668283	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs555109790	chr15:56668343-56668344	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs572781549	chr15:56668419-56668420	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs541464490	chr15:56668435-56668436	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs192694171	chr15:56668471-56668472	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs185591682	chr15:56668473-56668474	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs574887027	chr15:56668512-56668513	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs76159708	chr15:56668527-56668528	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs529307973	chr15:56668566-56668567	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs111467026	chr15:56668567-56668568	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs115553906	chr15:56668592-56668593	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs188872287	chr15:56668605-56668606	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs546403115	chr15:56668620-56668621	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs117379966	chr15:56668658-56668659	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs528789655	chr15:56668666-56668667	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs548206382	chr15:56668753-56668754	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs111810261	chr15:56668763-56668764	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs192182621	chr15:56668781-56668782	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs145868868	chr15:56668797-56668798	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs149023238	chr15:56668814-56668815	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs560433143	chr15:56668823-56668824	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs563763889	chr15:56668825-56668826	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs550371582	chr15:56668846-56668847	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:61)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Testicular germ cell tumor	18059402	CNVD
cataract	16735990	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Medulloblastoma	21979893	CNVD
spastic paraplegia with thinning of corpus callosum	19105190	CNVD
Schizophrenia	21324950	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Disease	21824424	CNVD
Melanoma	18172304	CNVD
Colorectal cancer	16774939	CNVD
Gastric cancer	17167181	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Colorectal cancer	16272173	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Multiple myeloma	17550852	CNVD
Intellectual disability	22102821	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	CNVD
Prostate cancer	16573809	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Multiple myeloma	20724749	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Basal cell lymphoma	17053054	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Cancer	21129771	CNVD
Breast cancer	16272173	CNVD
Hepatocellular carcinoma	16750200	CNVD
Abnormal phenotypes	18644119	CNVD
Cancer	16751803	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Acute monocytic leukemia	16498392	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Breast cancer	17133270	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Gastric adenocarcinoma	19115996	CNVD
Congenital diaphragmatic hernia	21341218	CNVD
Holoprosencephaly	21359414	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Glioblastoma multiforme	21510904	CNVD

Chromatin state (count:1174 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:56658200-56675400	Weak transcription	Pancreas	Pancrea
2	chr15:56658800-56669600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr15:56659600-56675400	Weak transcription	Rectal Mucosa Donor 29	rectum
4	chr15:56660400-56674400	Weak transcription	Hela-S3	cervix
5	chr15:56661000-56671000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr15:56661800-56668400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
7	chr15:56664400-56667600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
8	chr15:56664400-56669400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr15:56664400-56669600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
10	chr15:56664400-56685200	Weak transcription	Duodenum Mucosa	Duodenum
11	chr15:56665200-56733400	Weak transcription	Fetal Kidney	kidney
12	chr15:56666400-56667200	ZNF genes & repeats	GM12878-XiMat	blood
13	chr15:56666800-56667200	ZNF genes & repeats	H9 Derived Neuron Cultured Cells	ES cell derived
14	chr15:56666800-56667200	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
15	chr15:56667200-56668400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
16	chr15:56667200-56670400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr15:56670400-56672000	ZNF genes & repeats	H9 Derived Neuron Cultured Cells	ES cell derived
18	chr15:56670600-56673000	ZNF genes & repeats	Ganglion Eminence derived primary cultured neurospheres	brain
19	chr15:56670800-56671000	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
20	chr15:56671000-56671200	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin03	Skin
21	chr15:56671000-56672000	ZNF genes & repeats	GM12878-XiMat	blood
22	chr15:56671000-56676800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
23	chr15:56671400-56676200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
24	chr15:56671800-56672000	ZNF genes & repeats	Ovary	ovary
25	chr15:56672000-56673600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
26	chr15:56672000-56694600	Weak transcription	Ovary	ovary
27	chr15:56672400-56674000	Weak transcription	Thymus	Thymus
28	chr15:56672400-56677400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
29	chr15:56673000-56678000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
30	chr15:56673200-56677000	Weak transcription	Gastric	stomach
31	chr15:56673400-56675800	Weak transcription	Fetal Intestine Large	intestine
32	chr15:56673400-56676600	Weak transcription	Cortex derived primary cultured neurospheres	brain
33	chr15:56673600-56675200	ZNF genes & repeats	GM12878-XiMat	blood
34	chr15:56673600-56675400	ZNF genes & repeats	H9 Derived Neuron Cultured Cells	ES cell derived
35	chr15:56673600-56675400	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr15:56673800-56674000	ZNF genes & repeats	Fetal Intestine Small	intestine
37	chr15:56673800-56676800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr15:56674000-56675000	Strong transcription	Fetal Intestine Small	intestine
39	chr15:56674000-56675400	ZNF genes & repeats	Fetal Stomach	stomach
40	chr15:56674000-56675400	Strong transcription	Thymus	Thymus
41	chr15:56674200-56675000	Weak transcription	Fetal Lung	lung
42	chr15:56674800-56675600	Enhancers	HMEC	breast
43	chr15:56675000-56675200	ZNF genes & repeats	Fetal Lung	lung
44	chr15:56675000-56675800	Enhancers	Stomach Mucosa	stomach
45	chr15:56675000-56685000	Weak transcription	Fetal Intestine Small	intestine
46	chr15:56675200-56676200	Weak transcription	Fetal Lung	lung
47	chr15:56675200-56676600	Weak transcription	GM12878-XiMat	blood
48	chr15:56675400-56675600	Enhancers	Pancreas	Pancrea
49	chr15:56675400-56676400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
50	chr15:56675400-56676600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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