Variant report

Variant	nsv457211
Chromosome Location	chr15:82362125-82396347
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:550)
CpG islands
(count:306)
Chromatin interactive
region (count:18)
LncRNA
region (count:16)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:550 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:82395869-82396118	K562	blood:	n/a	n/a
2	ARID3A	chr15:82386098-82386477	K562	blood:	n/a	n/a
3	ARID3A	chr15:82374412-82374413	K562	blood:	n/a	n/a
4	ATF1	chr15:82368129-82368329	K562	blood:	n/a	n/a
5	ATF1	chr15:82386057-82386548	K562	blood:	n/a	n/a
6	ATF3	chr15:82386007-82386455	K562	blood:	n/a	n/a
7	BATF	chr15:82372902-82373188	GM12878	blood:	n/a	n/a
8	BCL3	chr15:82391074-82391291	GM12878	blood:	n/a	n/a
9	BHLHE40	chr15:82367932-82367944	K562	blood:	n/a	n/a
10	BHLHE40	chr15:82378992-82379159	K562	blood:	n/a	n/a
11	BHLHE40	chr15:82395922-82396071	K562	blood:	n/a	n/a
12	BHLHE40	chr15:82386095-82386510	K562	blood:	n/a	n/a
13	BHLHE40	chr15:82396298-82396499	K562	blood:	n/a	n/a
14	BHLHE40	chr15:82374424-82374533	K562	blood:	n/a	n/a
15	BRCA1	chr15:82386082-82386445	Hela-S3	cervix:	n/a	n/a
16	CBX3	chr15:82365191-82365641	K562	blood:	n/a	n/a
17	CBX3	chr15:82386086-82386521	K562	blood:	n/a	n/a
18	CCNT2	chr15:82374339-82374522	K562	blood:	n/a	n/a
19	CCNT2	chr15:82379090-82379273	K562	blood:	n/a	chr15:82379122-82379142
20	CCNT2	chr15:82386130-82386485	K562	blood:	n/a	n/a
21	CEBPB	chr15:82386011-82386541	IMR90	lung:	n/a	chr15:82386244-82386255
22	CEBPB	chr15:82386008-82386564	Hela-S3	cervix:	n/a	chr15:82386244-82386255
23	CEBPB	chr15:82392963-82393112	Hela-S3	cervix:	n/a	n/a
24	CEBPB	chr15:82386068-82386458	K562	blood:	n/a	chr15:82386244-82386255
25	CEBPB	chr15:82392940-82393048	H1-hESC	embryonic stem cell:	n/a	n/a
26	CEBPB	chr15:82386086-82386434	HepG2	liver:	n/a	chr15:82386244-82386255
27	CEBPB	chr15:82381317-82381476	HepG2	liver:	n/a	n/a
28	CEBPB	chr15:82395191-82395267	K562	blood:	n/a	n/a
29	CEBPB	chr15:82382298-82382448	A549	lung:	n/a	n/a
30	CEBPB	chr15:82395049-82395325	HepG2	liver:	n/a	n/a
31	CEBPB	chr15:82381200-82381390	IMR90	lung:	n/a	chr15:82381247-82381260
32	CEBPB	chr15:82383993-82384303	K562	blood:	n/a	n/a
33	CEBPB	chr15:82386025-82386510	K562	blood:	n/a	chr15:82386244-82386255
34	CEBPB	chr15:82383982-82384317	A549	lung:	n/a	n/a
35	CEBPB	chr15:82395084-82395398	A549	lung:	n/a	n/a
36	CEBPB	chr15:82395085-82395305	IMR90	lung:	n/a	n/a
37	CEBPB	chr15:82386054-82386470	A549	lung:	n/a	chr15:82386244-82386255
38	CEBPB	chr15:82386060-82386499	A549	lung:	n/a	chr15:82386244-82386255
39	CEBPB	chr15:82385996-82386610	A549	lung:	n/a	chr15:82386244-82386255
40	CEBPB	chr15:82383960-82384377	MCF-7	breast:	n/a	n/a
41	CEBPB	chr15:82386077-82386411	K562	blood:	n/a	chr15:82386244-82386255
42	CEBPB	chr15:82383979-82384330	IMR90	lung:	n/a	n/a
43	CHD2	chr15:82375437-82375518	K562	blood:	n/a	n/a
44	CHD2	chr15:82386096-82386442	K562	blood:	n/a	n/a
45	CHD2	chr15:82386096-82386465	HepG2	liver:	n/a	n/a
46	CHD2	chr15:82386056-82386507	Hela-S3	cervix:	n/a	n/a
47	CTCF	chr15:82395740-82395890	RPTEC	kidney:	n/a	chr15:82395834-82395842
48	CTCF	chr15:82395943-82396068	SK-N-SH_RA	brain:	n/a	chr15:82396008-82396016
49	CTCF	chr15:82374240-82374390	GM12873	blood:	n/a	n/a
50	CTCF	chr15:82395986-82396140	ProgFib	skin:	n/a	chr15:82396008-82396016

(count:306 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:82379883-82379933	HRCEpiC	kidney:	n/a
2	chr15:82379883-82379933	HRCEpiC	kidney:	n/a
3	chr15:82374456-82374506	LNCaP	prostate:	n/a
4	chr15:82379883-82379933	HRE	kidney:	n/a
5	chr15:82379883-82379933	AG09319	gingival:	n/a
6	chr15:82381568-82381618	NHDF-neo	bronchial:	n/a
7	chr15:82379947-82379997	Jurkat	blood:	n/a
8	chr15:82393236-82393286	HRE	kidney:	n/a
9	chr15:82393236-82393286	MCF-7	breast:	n/a
10	chr15:82393236-82393286	PFSK-1	brain:	n/a
11	chr15:82374456-82374506	ProgFib	skin:	n/a
12	chr15:82374456-82374506	AoSMC	blood vessel:	n/a
13	chr15:82379947-82379997	HIPEpiC	eye:	n/a
14	chr15:82379947-82379997	HCPEpiC	choroid plexus:	n/a
15	chr15:82374456-82374506	K562	blood:	n/a
16	chr15:82379947-82379997	HMEC	breast:	n/a
17	chr15:82379883-82379933	LNCaP	prostate:	n/a
18	chr15:82393236-82393286	AG09319	gingival:	n/a
19	chr15:82393236-82393286	ProgFib	skin:	n/a
20	chr15:82379883-82379933	T-47D	breast:	n/a
21	chr15:82393236-82393286	Jurkat	blood:	n/a
22	chr15:82379947-82379997	HCT-116	colon:	n/a
23	chr15:82379947-82379997	AG10803	skin:	n/a
24	chr15:82381568-82381618	AG04449	skin:	fetal
25	chr15:82374456-82374506	HUVEC	blood vessel:	n/a
26	chr15:82393236-82393286	Caco-2	colon:	n/a
27	chr15:82379883-82379933	MCF-7	breast:	n/a
28	chr15:82374456-82374506	NH-A	brain:	n/a
29	chr15:82374456-82374506	HCT-116	colon:	n/a
30	chr15:82379883-82379933	GM12878	blood:	n/a
31	chr15:82381568-82381618	GM19239	blood:	n/a
32	chr15:82374456-82374506	SK-N-MC	brain:	n/a
33	chr15:82379947-82379997	SKMC	muscle:	n/a
34	chr15:82379947-82379997	GM12892	blood:	n/a
35	chr15:82381568-82381618	HL-60	blood:	n/a
36	chr15:82379883-82379933	HEEpiC	esophagus:	n/a
37	chr15:82379947-82379997	SK-N-SH	brain:	n/a
38	chr15:82379883-82379933	HAEpiC	amniotic membrane:	n/a
39	chr15:82379947-82379997	RPTEC	kidney:	n/a
40	chr15:82374456-82374506	GM12878	blood:	n/a
41	chr15:82393236-82393286	ECC-1	luminal epithelium:	n/a
42	chr15:82374456-82374506	HCPEpiC	choroid plexus:	n/a
43	chr15:82374456-82374506	HCF	heart:	n/a
44	chr15:82381568-82381618	HUVEC	blood vessel:	n/a
45	chr15:82379883-82379933	HUVEC	blood vessel:	n/a
46	chr15:82379883-82379933	U87	brain:	n/a
47	chr15:82393236-82393286	AG09309	skin:	n/a
48	chr15:82381568-82381618	HCM	heart:	n/a
49	chr15:82379947-82379997	AoSMC	blood vessel:	n/a
50	chr15:82379947-82379997	Hela-S3	cervix:	n/a

(count:18 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:82357212..82358896-chr15:82360532..82363028,2	MCF-7	breast:
2	chr15:82376238..82379058-chr15:82380480..82382562,2	MCF-7	breast:
3	chr15:82330589..82332800-chr15:82367218..82368860,2	K562	blood:
4	chr15:82360547..82363017-chr15:82368630..82370323,2	K562	blood:
5	chr15:82338516..82340987-chr15:82386144..82387942,2	MCF-7	breast:
6	chr15:82105377..82106205-chr15:82395564..82396156,2	MCF-7	breast:
7	chr15:82358587..82361441-chr15:82362819..82366387,4	K562	blood:
8	chr15:82336857..82340285-chr15:82395789..82397569,3	MCF-7	breast:
9	chr15:82375697..82377432-chr15:82459942..82461886,2	K562	blood:
10	chr15:82394736..82396289-chr15:82399463..82401078,2	MCF-7	breast:
11	chr15:82342535..82345298-chr15:82361301..82363845,2	MCF-7	breast:
12	chr15:82345778..82347670-chr15:82359929..82362886,2	K562	blood:
13	chr15:82336811..82339430-chr15:82392148..82395651,3	MCF-7	breast:
14	chr15:82360547..82363017-chr15:82368630..82370323,2	K562	blood:
15	chr15:82390762..82392949-chr15:82398564..82402214,3	K562	blood:
16	chr15:82386362..82388607-chr15:82391684..82394477,4	K562	blood:
17	chr15:82396164..82398346-chr15:82406284..82408349,2	K562	blood:
18	chr15:82386362..82388607-chr15:82391684..82394477,4	K562	blood:

(count:16 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-597K23.2.1-2	chr15:82391746-82393834	XLOC_011331
2	lnc-RP11-597K23.2.1-1	chr15:82387823-82388777	ENSG00000249946
3	lnc-RP11-597K23.2.1-1	chr15:82386324-82386575	ENSG00000249946
4	lnc-RP11-597K23.2.1-2	chr15:82390245-82390326	NONHSAT047767
5	lnc-RP11-597K23.2.1-1	chr15:82386324-82386575	NONHSAT047766
6	lnc-RP11-597K23.2.1-1	chr15:82387823-82388777	NONHSAT047766
7	lnc-RP11-597K23.2.1-1	chr15:82385735-82385835	NONHSAT047766
8	lnc-RP11-597K23.2.1-1	chr15:82380935-82381069	ENSG00000249946
9	lnc-RP11-597K23.2.1-1	chr15:82389789-82390035	NONHSAT047766
10	lnc-RP11-597K23.2.1-1	chr15:82384068-82384945	NONHSAT047766
11	lnc-RP11-597K23.2.1-2	chr15:82390362-82395263	NONHSAT047767
12	lnc-RP11-597K23.2.1-1	chr15:82385735-82385835	ENSG00000249946
13	lnc-RP11-597K23.2.1-1	chr15:82380935-82381069	NONHSAT047766
14	lnc-RP11-597K23.2.1-1	chr15:82389789-82390032	ENSG00000249946
15	lnc-RP11-597K23.2.1-1	chr15:82384068-82384945	ENSG00000249946
16	lnc-RP11-597K23.2.1-2	chr15:82391267-82391320	XLOC_011331

No data

Variant related genes	Relation type
ENSG00000259518	TF binding region
ENSG00000259518	CpG island
ENSG00000183496	chromatin interactions
ENSG00000259518	chromatin interactions
C9orf5	miRNA target sites
PRRC1	miRNA target sites
LIMCH1	miRNA target sites
SUZ12	miRNA target sites

Extended variants
information (count: 1234 )
Associated
traits (count: 74 )

Variant overlapped rSNPs/rCNVs (count:1234 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2654191	chr15:82362125-82362126	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs540434084	chr15:82362129-82362130	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs76662553	chr15:82362160-82362161	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs74249832	chr15:82362181-82362182	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs372101665	chr15:82362184-82362185	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs375077143	chr15:82362205-82362206	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs554500147	chr15:82362206-82362207	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs147333856	chr15:82362302-82362303	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs536967506	chr15:82362317-82362318	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs556103248	chr15:82362350-82362351	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs2654192	chr15:82362352-82362353	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs112391197	chr15:82362376-82362377	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs193127829	chr15:82362398-82362399	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs184457538	chr15:82362419-82362420	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs572481661	chr15:82362442-82362443	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs527292720	chr15:82362475-82362476	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs371621675	chr15:82362484-82362485	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs189332166	chr15:82362534-82362535	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs530388157	chr15:82362562-82362563	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs550506814	chr15:82362564-82362565	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs563229896	chr15:82362594-82362595	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs5741735	chr15:82362616-82362617	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs3065106	chr15:82362636-82362637	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs141458188	chr15:82362638-82362639	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs532139207	chr15:82362646-82362647	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs374861025	chr15:82362771-82362772	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs151289867	chr15:82362776-82362777	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs372619798	chr15:82362798-82362799	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs565750072	chr15:82362834-82362835	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs111800071	chr15:82362867-82362868	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs548337290	chr15:82362884-82362885	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs140218144	chr15:82362900-82362901	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs568177168	chr15:82362923-82362924	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs536905236	chr15:82362935-82362936	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs372424277	chr15:82362987-82362988	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs556835587	chr15:82362999-82363000	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs570455716	chr15:82363032-82363033	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs184555842	chr15:82363036-82363037	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs149895632	chr15:82363037-82363038	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs77931224	chr15:82363053-82363054	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs541185232	chr15:82363054-82363055	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs548709765	chr15:82363107-82363108	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs555107233	chr15:82363120-82363121	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs188754040	chr15:82363128-82363129	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs544074818	chr15:82363184-82363185	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs563960207	chr15:82363243-82363244	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs181484086	chr15:82363251-82363252	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs370044118	chr15:82363321-82363322	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs371487486	chr15:82363360-82363361	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs545791370	chr15:82363364-82363365	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:74)

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
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
Hodgkin''s lymphoma	17606441	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Autism	17322880	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Lung cancer	18438408	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
Oral squamous cell carcinoma	17134496	CNVD
Colorectal cancer	16774939	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Sudden cardiac death	19188705	CNVD
Breast cancer	21990379	CNVD
Myelofibrosis	22110671	CNVD
Congenital diaphragmatic hernia	21341218	CNVD
Adenocarcinoma	19607727	CNVD
Squamous cell cancer	19607727	CNVD
Congenital diaphragmatic hernia	20921022	CNVD
abnormal development	18461090	CNVD
Intellectual disability	22102821	CNVD
renal disease	17924346	CNVD
Breast cancer	20409316	CNVD
Mental retardation	17847001	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21785460	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21509527	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:201 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:82356600-82364200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr15:82361200-82364000	Enhancers	K562	blood
3	chr15:82364000-82364400	Weak transcription	K562	blood
4	chr15:82364200-82366000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr15:82364400-82366200	Enhancers	K562	blood
6	chr15:82365400-82366000	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
7	chr15:82365600-82366000	Enhancers	H1 Cell Line	embryonic stem cell
8	chr15:82365600-82366000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
9	chr15:82365600-82366000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
10	chr15:82365800-82366000	Enhancers	HUES6 Cell Line	embryonic stem cell
11	chr15:82366000-82367800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr15:82366200-82367400	Weak transcription	K562	blood
13	chr15:82367400-82369000	Enhancers	K562	blood
14	chr15:82367800-82368200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr15:82367800-82368200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr15:82367800-82368800	Enhancers	Fetal Brain Male	brain
17	chr15:82368200-82368400	Bivalent Enhancer	Fetal Stomach	stomach
18	chr15:82368200-82368800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr15:82372000-82372600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
20	chr15:82372000-82372600	Enhancers	Fetal Lung	lung
21	chr15:82372000-82372600	Enhancers	Fetal Stomach	stomach
22	chr15:82372200-82372400	Enhancers	ES-I3 Cell Line	embryonic stem cell
23	chr15:82372200-82372400	Enhancers	HUES48 Cell Line	embryonic stem cell
24	chr15:82372200-82373000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
25	chr15:82372400-82372600	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
26	chr15:82372400-82373000	Enhancers	HSMMtube	muscle
27	chr15:82372600-82373600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
28	chr15:82372800-82374200	Weak transcription	HUES48 Cell Line	embryonic stem cell
29	chr15:82373000-82374200	Weak transcription	HSMMtube	muscle
30	chr15:82373000-82374400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
31	chr15:82373600-82374200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
32	chr15:82374000-82374400	Enhancers	Osteobl	bone
33	chr15:82374000-82375400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
34	chr15:82374200-82374800	Enhancers	HUES48 Cell Line	embryonic stem cell
35	chr15:82374200-82374800	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
36	chr15:82374200-82375000	Enhancers	H1 Cell Line	embryonic stem cell
37	chr15:82374200-82375400	Enhancers	HSMMtube	muscle
38	chr15:82374200-82375400	Enhancers	NH-A	brain
39	chr15:82374200-82376000	Enhancers	HSMM	muscle
40	chr15:82374400-82374800	Enhancers	ES-I3 Cell Line	embryonic stem cell
41	chr15:82374400-82375000	Enhancers	HUES6 Cell Line	embryonic stem cell
42	chr15:82374400-82375000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
43	chr15:82374400-82375000	Enhancers	iPS-15b Cell Line	embryonic stem cell
44	chr15:82374400-82375000	Flanking Active TSS	Osteobl	bone
45	chr15:82374400-82375200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
46	chr15:82374400-82375400	Enhancers	Muscle Satellite Cultured Cells	--
47	chr15:82374600-82374800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
48	chr15:82374600-82374800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
49	chr15:82374600-82374800	Enhancers	K562	blood
50	chr15:82374600-82375000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived

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