Variant report

Variant	nsv974572
Chromosome Location	chr15:49448277-49450621
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:160)
CpG islands
(count:184)
Chromatin interactive
region (count:7)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:160 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr15:49447664-49448284	K562	blood:	n/a	n/a
2	BHLHE40	chr15:49447353-49448422	HepG2	liver:	n/a	chr15:49447555-49447571
3	BRCA1	chr15:49447295-49448343	Hela-S3	cervix:	n/a	n/a
4	CBX3	chr15:49447510-49448320	HCT-116	colon:	n/a	n/a
5	CBX3	chr15:49447538-49448393	K562	blood:	n/a	n/a
6	CEBPB	chr15:49448461-49448675	IMR90	lung:	n/a	n/a
7	CEBPB	chr15:49448513-49448762	Hela-S3	cervix:	n/a	n/a
8	CHD1	chr15:49448271-49448311	H1-hESC	embryonic stem cell:	n/a	n/a
9	CHD2	chr15:49448461-49448661	HepG2	liver:	n/a	n/a
10	CREB1	chr15:49447497-49448350	GM12878	blood:	n/a	n/a
11	CUX1	chr15:49447723-49448280	GM12878	blood:	n/a	n/a
12	ELF1	chr15:49447548-49448315	HCT-116	colon:	n/a	chr15:49447550-49447562
13	ELK1	chr15:49447667-49448310	GM12878	blood:	n/a	n/a
14	ELK1	chr15:49448740-49448746	Hela-S3	cervix:	n/a	n/a
15	ELK1	chr15:49447385-49448299	Hela-S3	cervix:	n/a	n/a
16	ELK4	chr15:49447609-49448321	Hela-S3	cervix:	n/a	n/a
17	EP300	chr15:49448721-49448754	GM12878	blood:	n/a	n/a
18	GABPA	chr15:49447419-49448827	SK-N-SH	brain:	n/a	n/a
19	GABPA	chr15:49447555-49448353	HL-60	blood:	n/a	n/a
20	GABPA	chr15:49447497-49448284	K562	blood:	n/a	n/a
21	GABPA	chr15:49447520-49448400	A549	lung:	n/a	n/a
22	GABPA	chr15:49447437-49448350	SK-N-SH	brain:	n/a	n/a
23	GABPA	chr15:49447447-49448447	A549	lung:	n/a	n/a
24	GABPA	chr15:49447475-49448302	MCF-7	breast:	n/a	n/a
25	GABPA	chr15:49447208-49448655	MCF-7	breast:	n/a	n/a
26	GABPA	chr15:49447288-49448530	HL-60	blood:	n/a	n/a
27	GATA1	chr15:49447019-49448881	PBDE	blood:	n/a	n/a
28	GATA3	chr15:49448491-49448841	T-47D	breast:	n/a	n/a
29	HCFC1	chr15:49446184-49448992	Hela-S3	cervix:	n/a	n/a
30	HCFC1	chr15:49447204-49448302	K562	blood:	n/a	n/a
31	HEY1	chr15:49447483-49448297	K562	blood:	n/a	n/a
32	HEY1	chr15:49449328-49449520	K562	blood:	n/a	n/a
33	IRF1	chr15:49449315-49449538	K562	blood:	n/a	chr15:49449435-49449449 chr15:49449438-49449455 chr15:49449444-49449461 chr15:49449441-49449455 chr15:49449445-49449456
34	IRF1	chr15:49447610-49448364	K562	blood:	n/a	n/a
35	IRF1	chr15:49447536-49448340	K562	blood:	n/a	n/a
36	IRF1	chr15:49449303-49449497	K562	blood:	n/a	chr15:49449435-49449449 chr15:49449438-49449455 chr15:49449444-49449461 chr15:49449441-49449455 chr15:49449445-49449456
37	IRF4	chr15:49447566-49448284	GM12878	blood:	n/a	n/a
38	JUND	chr15:49448556-49448746	K562	blood:	n/a	n/a
39	JUND	chr15:49447022-49448334	H1-hESC	embryonic stem cell:	n/a	chr15:49447083-49447097
40	KAP1	chr15:49447524-49448452	HEK293	kidney:	n/a	n/a
41	MAFK	chr15:49447572-49448281	K562	blood:	n/a	chr15:49447804-49447819
42	MAFK	chr15:49448767-49448789	Hela-S3	cervix:	n/a	n/a
43	MAFK	chr15:49447347-49448488	Hela-S3	cervix:	n/a	chr15:49447804-49447819
44	MAX	chr15:49447179-49448660	NB4	blood:	n/a	n/a
45	MAX	chr15:49447195-49448320	ECC-1	luminal epithelium:	n/a	n/a
46	MAX	chr15:49447424-49448358	GM12878	blood:	n/a	n/a
47	MAX	chr15:49447371-49448328	ECC-1	luminal epithelium:	n/a	n/a
48	MAX	chr15:49447352-49448322	SK-N-SH	brain:	n/a	n/a
49	MAX	chr15:49447286-49448282	SK-N-SH	brain:	n/a	n/a
50	MAX	chr15:49447198-49448292	A549	lung:	n/a	n/a

(count:184 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:49448261-49448311	U87	brain:	n/a
2	chr15:49448261-49448311	U87	brain:	n/a
3	chr15:49449690-49449740	SK-N-SH_RA	brain:	n/a
4	chr15:49449690-49449740	HIPEpiC	eye:	n/a
5	chr15:49449690-49449740	T-47D	breast:	n/a
6	chr15:49448572-49448622	NT2-D1	testis:	n/a
7	chr15:49448572-49448622	T-47D	breast:	n/a
8	chr15:49448572-49448622	ECC-1	luminal epithelium:	n/a
9	chr15:49449690-49449740	ProgFib	skin:	n/a
10	chr15:49448261-49448311	GM12878	blood:	n/a
11	chr15:49449690-49449740	HUVEC	blood vessel:	n/a
12	chr15:49448572-49448622	BE2_C	brain:	n/a
13	chr15:49449690-49449740	Jurkat	blood:	n/a
14	chr15:49448572-49448622	PFSK-1	brain:	n/a
15	chr15:49449690-49449740	HRCEpiC	kidney:	n/a
16	chr15:49449690-49449740	K562	blood:	n/a
17	chr15:49449690-49449740	HMEC	breast:	n/a
18	chr15:49448572-49448622	AG04450	lung:	fetal
19	chr15:49448572-49448622	AoSMC	blood vessel:	n/a
20	chr15:49448572-49448622	NHBE	bronchial:	n/a
21	chr15:49448261-49448311	GM06990	blood:	n/a
22	chr15:49449690-49449740	NHBE	bronchial:	n/a
23	chr15:49449690-49449740	SK-N-MC	brain:	n/a
24	chr15:49449690-49449740	GM19239	blood:	n/a
25	chr15:49449690-49449740	HCF	heart:	n/a
26	chr15:49448572-49448622	SK-N-MC	brain:	n/a
27	chr15:49448261-49448311	RPTEC	kidney:	n/a
28	chr15:49448261-49448311	HCM	heart:	n/a
29	chr15:49448572-49448622	HRCEpiC	kidney:	n/a
30	chr15:49448572-49448622	GM12892	blood:	n/a
31	chr15:49449690-49449740	H1-hESC	embryonic stem cell:	embryo
32	chr15:49448261-49448311	GM12892	blood:	n/a
33	chr15:49449690-49449740	AG04449	skin:	fetal
34	chr15:49449690-49449740	GM06990	blood:	n/a
35	chr15:49448261-49448311	MCF-7	breast:	n/a
36	chr15:49449690-49449740	AG04450	lung:	fetal
37	chr15:49448572-49448622	Caco-2	colon:	n/a
38	chr15:49449690-49449740	RPTEC	kidney:	n/a
39	chr15:49448261-49448311	SKMC	muscle:	n/a
40	chr15:49448261-49448311	HL-60	blood:	n/a
41	chr15:49448572-49448622	HPAEpiC	pulmonary alveolar:	n/a
42	chr15:49448261-49448311	NB4	blood:	n/a
43	chr15:49449690-49449740	NB4	blood:	n/a
44	chr15:49449690-49449740	HL-60	blood:	n/a
45	chr15:49448261-49448311	HCT-116	colon:	n/a
46	chr15:49448261-49448311	HEK293	kidney:	embryo
47	chr15:49449690-49449740	Caco-2	colon:	n/a
48	chr15:49448572-49448622	HEK293	kidney:	embryo
49	chr15:49449690-49449740	Hela-S3	cervix:	n/a
50	chr15:49448572-49448622	HCM	heart:	n/a

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:49424882..49426670-chr15:49449093..49451869,2	MCF-7	breast:
2	chr15:49450612..49452294-chr15:49454611..49456431,2	K562	blood:
3	chr15:49446244..49450190-chr15:50645448..50647621,4	K562	blood:
4	chr15:49443824..49452367-chr15:49460648..49465189,20	K562	blood:
5	chr15:49446083..49452367-chr15:49460693..49464702,19	K562	blood:
6	chr15:49446471..49449731-chr15:49460521..49465602,13	MCF-7	breast:
7	chr15:49445500..49449019-chr15:49469042..49472548,3	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FGF7-3	chr15:49448495-49450822	NR_036507

No data

Variant related genes	Relation type
NDUFAF4P1	TF binding region
COPS2	TF binding region
NDUFAF4P1	CpG island
COPS2	CpG island
ENSG00000264210	chromatin interactions
ENSG00000104064	chromatin interactions
ENSG00000156958	chromatin interactions
ENSG00000259545	chromatin interactions
ENSG00000244879	chromatin interactions

Extended variants
information (count: 66 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:66 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs375287801	chr15:49448289-49448290	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
2	rs546067692	chr15:49448313-49448314	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
3	rs564374438	chr15:49448346-49448347	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
4	rs185397642	chr15:49448388-49448389	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
5	rs191165028	chr15:49448412-49448413	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
6	rs561995948	chr15:49448450-49448451	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
7	rs528914149	chr15:49448451-49448452	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
8	rs529299892	chr15:49448462-49448463	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
9	rs573087613	chr15:49448473-49448474	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
10	rs550738176	chr15:49448489-49448490	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
11	rs17426226	chr15:49448490-49448491	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs530852757	chr15:49448573-49448574	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
13	rs552481885	chr15:49448623-49448624	Active TSS Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
14	rs56131921	chr15:49448789-49448790	Active TSS Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
15	rs114832326	chr15:49448811-49448812	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
16	rs534489693	chr15:49448829-49448830	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
17	rs543152347	chr15:49448838-49448839	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
18	rs182961888	chr15:49448855-49448856	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
19	rs568022763	chr15:49448905-49448906	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
20	rs72727224	chr15:49448908-49448909	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region lncRNA	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs556568735	chr15:49448950-49448951	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
22	rs188455615	chr15:49448985-49448986	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
23	rs546104632	chr15:49449062-49449063	Weak transcription Active TSS Flanking Active TSS Enhancers	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
24	rs528912420	chr15:49449069-49449070	Weak transcription Active TSS Flanking Active TSS Enhancers	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
25	rs573391329	chr15:49449073-49449074	Weak transcription Active TSS Flanking Active TSS Enhancers	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
26	rs540433267	chr15:49449086-49449087	Weak transcription Active TSS Flanking Active TSS Enhancers	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
27	rs61442055	chr15:49449098-49449099	Weak transcription Active TSS Flanking Active TSS Enhancers	Chromatin interactive region lncRNA	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
28	rs529411528	chr15:49449173-49449174	Weak transcription Active TSS Flanking Active TSS Enhancers	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
29	rs542911975	chr15:49449234-49449235	Weak transcription Active TSS Flanking Active TSS Enhancers	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
30	rs544693742	chr15:49449270-49449271	Weak transcription Active TSS Flanking Active TSS Enhancers	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
31	rs114461306	chr15:49449291-49449292	Weak transcription Active TSS Flanking Active TSS Enhancers	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
32	rs562580056	chr15:49449353-49449354	Weak transcription Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
33	rs192813648	chr15:49449363-49449364	Weak transcription Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
34	rs552520947	chr15:49449390-49449391	Weak transcription Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
35	rs570606805	chr15:49449465-49449466	Weak transcription Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
36	rs140318835	chr15:49449470-49449471	Weak transcription Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
37	rs370730212	chr15:49449491-49449492	Weak transcription Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
38	rs559195290	chr15:49449530-49449531	Weak transcription Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
39	rs145563567	chr15:49449685-49449686	Weak transcription Active TSS Enhancers Flanking Active TSS	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
40	rs375256123	chr15:49449717-49449718	Weak transcription Active TSS Enhancers Flanking Active TSS	CpG island Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
41	rs138084915	chr15:49449719-49449720	Weak transcription Active TSS Enhancers Flanking Active TSS	CpG island Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
42	rs556606096	chr15:49449744-49449745	Weak transcription Active TSS Enhancers Flanking Active TSS	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
43	rs149467733	chr15:49449778-49449779	Weak transcription Active TSS Enhancers Flanking Active TSS	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
44	rs143017205	chr15:49449861-49449862	Weak transcription Active TSS Enhancers Flanking Active TSS	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
45	rs56259196	chr15:49449892-49449893	Weak transcription Active TSS Enhancers Flanking Active TSS	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
46	rs528285430	chr15:49449987-49449988	Weak transcription Active TSS Enhancers Flanking Active TSS	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
47	rs558042024	chr15:49449990-49449991	Weak transcription Active TSS Enhancers Flanking Active TSS	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
48	rs550294027	chr15:49449994-49449995	Weak transcription Active TSS Enhancers Flanking Active TSS	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
49	rs116534761	chr15:49450056-49450057	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
50	rs369219633	chr15:49450090-49450091	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:62)

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
Breast cancer	21785460	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Basal cell lymphoma	17053054	CNVD
Breast cancer	22032731	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Hirschsprung''s Disease	21712996	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Cancer	21129771	CNVD
Breast cancer	16272173	CNVD
Hepatocellular carcinoma	16750200	CNVD
Abnormal phenotypes	18644119	CNVD
Cancer	16751803	CNVD
Acute myeloid leukemia	19651601	CNVD
Marfan syndrome	17492313	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Myelofibrosis	22110671	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	21364760	CNVD
Aromatase excess syndrome	21470988	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:363 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:49445400-49449000	Active TSS	Breast Myoepithelial Primary Cells	Breast
2	chr15:49445600-49449200	Active TSS	iPS-20b Cell Line	embryonic stem cell
3	chr15:49445800-49449000	Active TSS	iPS-15b Cell Line	embryonic stem cell
4	chr15:49445800-49449200	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr15:49445800-49449200	Active TSS	HUES64 Cell Line	embryonic stem cell
6	chr15:49445800-49450400	Active TSS	NHLF	lung
7	chr15:49446000-49448800	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
8	chr15:49446000-49449000	Active TSS	H1 Cell Line	embryonic stem cell
9	chr15:49446000-49449400	Active TSS	K562	blood
10	chr15:49446000-49449600	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
11	chr15:49446000-49450000	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr15:49446200-49448800	Active TSS	iPS-18 Cell Line	embryonic stem cell
13	chr15:49446200-49448800	Active TSS	Hela-S3	cervix
14	chr15:49446200-49449000	Active TSS	ES-I3 Cell Line	embryonic stem cell
15	chr15:49446200-49449000	Active TSS	HUES6 Cell Line	embryonic stem cell
16	chr15:49446200-49449000	Flanking Active TSS	Primary hematopoietic stem cells	blood
17	chr15:49446200-49449200	Active TSS	A549	lung
18	chr15:49446200-49449600	Active TSS	NHDF-Ad	bronchial
19	chr15:49446400-49449000	Active TSS	Muscle Satellite Cultured Cells	--
20	chr15:49446400-49449000	Active TSS	Right Atrium	heart
21	chr15:49446400-49449000	Active TSS	Osteobl	bone
22	chr15:49446400-49449200	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
23	chr15:49446400-49449200	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
24	chr15:49446400-49449600	Active TSS	HMEC	breast
25	chr15:49446400-49450400	Active TSS	GM12878-XiMat	blood
26	chr15:49446600-49448600	Active TSS	Fetal Lung	lung
27	chr15:49446600-49448600	Active TSS	Right Ventricle	heart
28	chr15:49446600-49448800	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
29	chr15:49446600-49448800	Active TSS	Ovary	ovary
30	chr15:49446600-49449000	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
31	chr15:49446600-49449000	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr15:49446600-49449000	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
33	chr15:49446600-49449000	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
34	chr15:49446600-49449000	Active TSS	Fetal Adrenal Gland	Adrenal Gland
35	chr15:49446600-49449000	Active TSS	Fetal Intestine Small	intestine
36	chr15:49446600-49449000	Active TSS	Pancreatic Islets	Pancreatic Islet
37	chr15:49446600-49449000	Active TSS	Fetal Muscle Leg	muscle
38	chr15:49446600-49449000	Active TSS	Psoas Muscle	Psoas
39	chr15:49446600-49449000	Active TSS	HSMM	muscle
40	chr15:49446600-49449000	Active TSS	HSMMtube	muscle
41	chr15:49446600-49449000	Active TSS	NHEK	skin
42	chr15:49446600-49449200	Active TSS	HUES48 Cell Line	embryonic stem cell
43	chr15:49446600-49449200	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
44	chr15:49446600-49449200	Active TSS	Fetal Thymus	thymus
45	chr15:49446600-49449400	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
46	chr15:49446600-49449600	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
47	chr15:49446600-49450000	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
48	chr15:49446800-49448400	Active TSS	Primary T helper cells PMA-I stimulated	--
49	chr15:49446800-49448600	Active TSS	Brain Inferior Temporal Lobe	brain
50	chr15:49446800-49448600	Active TSS	Placenta	Placenta

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