Variant report

Variant	nsv569970
Chromosome Location	chr15:74016622-74059081
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:215)
CpG islands
(count:1220)
Chromatin interactive
region (count:27)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:215 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr15:74019732-74020032	K562	blood:	n/a	n/a
2	BACH1	chr15:74044777-74044983	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr15:74016723-74016904	H1-hESC	embryonic stem cell:	n/a	n/a
4	CEBPB	chr15:74047834-74048089	Hela-S3	cervix:	n/a	n/a
5	CEBPB	chr15:74037767-74037886	H1-hESC	embryonic stem cell:	n/a	n/a
6	CEBPB	chr15:74037743-74037896	K562	blood:	n/a	n/a
7	CEBPB	chr15:74037667-74037989	HepG2	liver:	n/a	n/a
8	CEBPB	chr15:74035329-74035638	Hela-S3	cervix:	n/a	n/a
9	CEBPB	chr15:74037698-74037897	Hela-S3	cervix:	n/a	n/a
10	CEBPB	chr15:74041308-74041655	HepG2	liver:	n/a	chr15:74041474-74041485
11	CEBPB	chr15:74041339-74041615	A549	lung:	n/a	chr15:74041474-74041485
12	CEBPB	chr15:74037707-74037987	A549	lung:	n/a	n/a
13	CEBPB	chr15:74041389-74041634	IMR90	lung:	n/a	chr15:74041474-74041485
14	CEBPB	chr15:74037663-74037973	IMR90	lung:	n/a	n/a
15	CEBPB	chr15:74041451-74041506	Hela-S3	cervix:	n/a	chr15:74041474-74041485
16	CEBPB	chr15:74026926-74027092	HepG2	liver:	n/a	chr15:74027018-74027029
17	CEBPZ	chr15:74034208-74034214	HepG2	liver:	n/a	n/a
18	CHD1	chr15:74044765-74044802	H1-hESC	embryonic stem cell:	n/a	n/a
19	CHD2	chr15:74046208-74046595	H1-hESC	embryonic stem cell:	n/a	n/a
20	CHD2	chr15:74031692-74031745	HepG2	liver:	n/a	n/a
21	CHD2	chr15:74049446-74049533	H1-hESC	embryonic stem cell:	n/a	n/a
22	CTBP2	chr15:74043771-74044193	H1-hESC	embryonic stem cell:	n/a	n/a
23	CTCF	chr15:74019740-74019890	AoAF	blood vessel:	n/a	n/a
24	CTCF	chr15:74019660-74019810	HPAF	blood vessel:	n/a	n/a
25	CTCF	chr15:74034820-74034970	MCF-7	breast:	n/a	n/a
26	CTCF	chr15:74030600-74030750	GM12872	blood:	n/a	n/a
27	CTCF	chr15:74035660-74035810	HEK293	kidney:	n/a	n/a
28	CTCF	chr15:74019760-74019910	AG04449	skin:	n/a	n/a
29	CTCF	chr15:74019808-74019839	IMR90	lung:	n/a	n/a
30	CTCF	chr15:74034940-74035090	GM12870	blood:	n/a	n/a
31	CTCF	chr15:74035680-74035830	AG10803	skin:	n/a	n/a
32	CTCF	chr15:74035720-74035870	AG10803	skin:	n/a	n/a
33	CTCF	chr15:74019640-74019790	HFF	foreskin:	n/a	n/a
34	CTCF	chr15:74034960-74035110	WI-38	lung:	n/a	n/a
35	CTCF	chr15:74056380-74056530	GM12874	blood:	n/a	n/a
36	CTCF	chr15:74030060-74030210	SK-N-SH_RA	brain:	n/a	n/a
37	CTCF	chr15:74035680-74035830	HepG2	liver:	n/a	n/a
38	CTCF	chr15:74035620-74035770	MCF-7	breast:	n/a	n/a
39	CTCF	chr15:74031720-74031870	HEK293	kidney:	n/a	n/a
40	CTCF	chr15:74034840-74034990	HepG2	liver:	n/a	n/a
41	CTCF	chr15:74046288-74046318	Kidney_OC	kidney:	n/a	n/a
42	CTCF	chr15:74035660-74035810	MCF-7	breast:	n/a	n/a
43	CTCF	chr15:74035680-74035830	RPTEC	kidney:	n/a	n/a
44	CTCF	chr15:74019660-74019810	HBMEC	blood vessel:	n/a	n/a
45	CTCF	chr15:74019800-74019950	AG09309	skin:	n/a	n/a
46	CTCF	chr15:74019700-74019850	HCFaa	heart:	n/a	n/a
47	CTCF	chr15:74029980-74030130	SK-N-SH_RA	brain:	n/a	n/a
48	E2F6	chr15:74036509-74037082	H1-hESC	embryonic stem cell:	n/a	n/a
49	ELF1	chr15:74050953-74051386	K562	blood:	n/a	chr15:74051184-74051197
50	ELF1	chr15:74050964-74051408	GM12878	blood:	n/a	chr15:74051184-74051197

(count:1220 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:74031640-74031690	HPAEpiC	pulmonary alveolar:	n/a
2	chr15:74033803-74033853	U87	brain:	n/a
3	chr15:74023790-74023840	ECC-1	luminal epithelium:	n/a
4	chr15:74045083-74045133	BE2_C	brain:	n/a
5	chr15:74044539-74044589	AG04450	lung:	fetal
6	chr15:74023856-74023906	NT2-D1	testis:	n/a
7	chr15:74040580-74040630	AG04450	lung:	fetal
8	chr15:74046708-74046758	PFSK-1	brain:	n/a
9	chr15:74023790-74023840	NHBE	bronchial:	n/a
10	chr15:74045075-74045125	LNCaP	prostate:	n/a
11	chr15:74045705-74045755	HRPEpiC	eye:	n/a
12	chr15:74046708-74046758	MCF-7	breast:	n/a
13	chr15:74031640-74031690	SK-N-SH	brain:	n/a
14	chr15:74045083-74045133	HCF	heart:	n/a
15	chr15:74033803-74033853	PrEC	prostate:	n/a
16	chr15:74044815-74044865	A549	lung:	n/a
17	chr15:74044815-74044865	HCT-116	colon:	n/a
18	chr15:74024097-74024147	Hepatocyte	liver:	n/a
19	chr15:74024097-74024147	GM12878	blood:	n/a
20	chr15:74048800-74048850	HAEpiC	amniotic membrane:	n/a
21	chr15:74045083-74045133	GM12892	blood:	n/a
22	chr15:74043577-74043627	GM12892	blood:	n/a
23	chr15:74043456-74043506	HAEpiC	amniotic membrane:	n/a
24	chr15:74020186-74020236	HCPEpiC	choroid plexus:	n/a
25	chr15:74045075-74045125	AoSMC	blood vessel:	n/a
26	chr15:74040580-74040630	CMK	blood:	n/a
27	chr15:74024097-74024147	NHBE	bronchial:	n/a
28	chr15:74025634-74025684	HMEC	breast:	n/a
29	chr15:74043456-74043506	HCM	heart:	n/a
30	chr15:74045705-74045755	GM12892	blood:	n/a
31	chr15:74031640-74031690	HEK293	kidney:	embryo
32	chr15:74037743-74037793	LNCaP	prostate:	n/a
33	chr15:74033803-74033853	CMK	blood:	n/a
34	chr15:74020186-74020236	AG09309	skin:	n/a
35	chr15:74044539-74044589	NHBE	bronchial:	n/a
36	chr15:74043401-74043451	HL-60	blood:	n/a
37	chr15:74046708-74046758	PrEC	prostate:	n/a
38	chr15:74023790-74023840	HepG2	liver:	n/a
39	chr15:74024097-74024147	HCPEpiC	choroid plexus:	n/a
40	chr15:74020186-74020236	HIPEpiC	eye:	n/a
41	chr15:74045624-74045674	A549	lung:	n/a
42	chr15:74025634-74025684	MCF-7	breast:	n/a
43	chr15:74043456-74043506	HMEC	breast:	n/a
44	chr15:74031640-74031690	ovcar-3	ovarian:	n/a
45	chr15:74045705-74045755	SK-N-SH	brain:	n/a
46	chr15:74023856-74023906	Jurkat	blood:	n/a
47	chr15:74045705-74045755	IMR90	lung:	fetal
48	chr15:74033803-74033853	HEEpiC	esophagus:	n/a
49	chr15:74043401-74043451	BE2_C	brain:	n/a
50	chr15:74045624-74045674	RPTEC	kidney:	n/a

(count:27 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:74002150..74003130-chr15:74034989..74036028,29	MCF-7	breast:
2	chr15:74038183..74040978-chr15:74046386..74048785,2	MCF-7	breast:
3	chr15:74048802..74051099-chr15:74051112..74054086,2	K562	blood:
4	chr15:74002181..74003130-chr15:74035048..74036007,13	MCF-7	breast:
5	chr15:74002220..74002792-chr15:74019672..74020532,2	MCF-7	breast:
6	chr15:74028603..74030276-chr15:74032306..74034900,2	K562	blood:
7	chr15:74002207..74002895-chr15:74022574..74023389,3	MCF-7	breast:
8	chr15:74046017..74047520-chr15:74054449..74056140,2	MCF-7	breast:
9	chr15:74006471..74009141-chr15:74023643..74026024,2	MCF-7	breast:
10	chr15:74005160..74008724-chr15:74017261..74021043,5	MCF-7	breast:
11	chr15:74043669..74047390-chr15:74050985..74053950,3	MCF-7	breast:
12	chr15:74038183..74040978-chr15:74046386..74048785,2	MCF-7	breast:
13	chr15:74011149..74013454-chr15:74025485..74028084,2	K562	blood:
14	chr15:73924327..73926958-chr15:74019144..74021513,2	MCF-7	breast:
15	chr15:74027005..74029312-chr15:74030606..74032351,2	MCF-7	breast:
16	chr15:74046017..74047520-chr15:74054449..74056140,2	MCF-7	breast:
17	chr15:74037382..74039248-chr15:74049351..74051185,2	MCF-7	breast:
18	chr15:74037382..74039248-chr15:74049351..74051185,2	MCF-7	breast:
19	chr15:74030034..74031560-chr15:74044779..74046637,2	MCF-7	breast:
20	chr15:74017850..74020040-chr15:74025294..74027603,2	MCF-7	breast:
21	chr15:74010865..74012941-chr15:74017223..74020118,2	MCF-7	breast:
22	chr15:74048802..74051099-chr15:74051112..74054086,2	K562	blood:
23	chr15:74033365..74035153-chr15:74042394..74044937,2	MCF-7	breast:
24	chr15:74027005..74029312-chr15:74030606..74032351,2	MCF-7	breast:
25	chr15:74002347..74003098-chr15:74034906..74035966,3	MCF-7	breast:
26	chr15:74026974..74029000-chr15:74067503..74070280,2	MCF-7	breast:
27	chr15:74017850..74020040-chr15:74025294..74027603,2	MCF-7	breast:

(count:3 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C15orf59-2	chr15:74045697-74046276	NONHSAT047155
2	lnc-CD276-2	chr15:74044453-74044737	XLOC_011305
3	lnc-C15orf59-2	chr15:74052127-74052151	NONHSAT047155

No data

Variant related genes	Relation type
ENSG00000260469	TF binding region
C15orf59	TF binding region
ENSG00000260469	CpG island
C15orf59	CpG island
ENSG00000156642	chromatin interactions
ENSG00000205363	chromatin interactions

Extended variants
information (count: 1861 )
Associated
traits (count: 77 )

Variant overlapped rSNPs/rCNVs (count:1861 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4886520	chr15:74016622-74016623	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs551048370	chr15:74016641-74016642	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
3	rs569041250	chr15:74016666-74016667	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
4	rs79471034	chr15:74016667-74016668	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
5	rs551971776	chr15:74016727-74016728	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
6	rs560483809	chr15:74016728-74016729	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
7	rs375151915	chr15:74016731-74016732	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
8	rs74023515	chr15:74016738-74016739	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
9	rs552655525	chr15:74016804-74016805	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs369681004	chr15:74016806-74016807	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs529288711	chr15:74016816-74016817	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs1351160	chr15:74016853-74016854	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs144522401	chr15:74016885-74016886	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs150685573	chr15:74016886-74016887	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs557077184	chr15:74016892-74016893	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs139910566	chr15:74016899-74016900	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs1351161	chr15:74016903-74016904	Enhancers Weak transcription Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs149822714	chr15:74016917-74016918	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs188745844	chr15:74016933-74016934	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs565574624	chr15:74016994-74016995	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs562846916	chr15:74017016-74017017	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs4886892	chr15:74017058-74017059	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs145786201	chr15:74017112-74017113	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs544237255	chr15:74017115-74017116	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs369027911	chr15:74017123-74017124	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs111386098	chr15:74017126-74017127	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs562610805	chr15:74017132-74017133	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs141650580	chr15:74017154-74017155	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs532781221	chr15:74017156-74017157	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs181210213	chr15:74017158-74017159	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs528315803	chr15:74017186-74017187	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs145408253	chr15:74017201-74017202	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs79495503	chr15:74017202-74017203	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs571143006	chr15:74017206-74017207	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs568297875	chr15:74017209-74017210	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs527560739	chr15:74017259-74017260	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs147672047	chr15:74017261-74017262	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs539546403	chr15:74017271-74017272	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs142328803	chr15:74017338-74017339	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs547310390	chr15:74017387-74017388	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs4886896	chr15:74017409-74017410	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs527882719	chr15:74017426-74017427	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs528863510	chr15:74017430-74017431	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs540496314	chr15:74017442-74017443	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs556011613	chr15:74017468-74017469	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs574270813	chr15:74017469-74017470	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs184654120	chr15:74017471-74017472	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs143619585	chr15:74017506-74017507	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs533213761	chr15:74017508-74017509	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs545091314	chr15:74017513-74017514	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:77)

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
Lung cancer	18438408	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
Gastrointestinal stromal cancer	20877625	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
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Bipolar disorder	19114987	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Cancer	20164919	CNVD

Chromatin state (count:835 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:73990600-74018800	Weak transcription	Right Atrium	heart
2	chr15:74007400-74031400	Weak transcription	Cortex derived primary cultured neurospheres	brain
3	chr15:74009400-74018400	Weak transcription	Left Ventricle	heart
4	chr15:74012800-74018600	Weak transcription	Right Ventricle	heart
5	chr15:74015200-74017200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr15:74015400-74017200	Enhancers	Fetal Lung	lung
7	chr15:74015600-74017000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
8	chr15:74015800-74017200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr15:74015800-74017200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr15:74015800-74033400	Weak transcription	Ovary	ovary
11	chr15:74016400-74016800	Enhancers	ES-I3 Cell Line	embryonic stem cell
12	chr15:74016400-74016800	Enhancers	Fetal Heart	heart
13	chr15:74016600-74016800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr15:74016600-74016800	Enhancers	HUES6 Cell Line	embryonic stem cell
15	chr15:74016600-74016800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr15:74016600-74016800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
17	chr15:74016600-74016800	Flanking Active TSS	Lung	lung
18	chr15:74016600-74016800	Enhancers	Spleen	Spleen
19	chr15:74016600-74016800	Bivalent Enhancer	Hela-S3	cervix
20	chr15:74016800-74017000	Active TSS	Lung	lung
21	chr15:74016800-74019400	Weak transcription	Fetal Heart	heart
22	chr15:74017200-74020000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr15:74018400-74021800	Enhancers	Left Ventricle	heart
24	chr15:74018600-74019800	Enhancers	Right Ventricle	heart
25	chr15:74018800-74019600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
26	chr15:74018800-74019800	Enhancers	Right Atrium	heart
27	chr15:74019400-74019800	Enhancers	NH-A	brain
28	chr15:74019400-74020800	Enhancers	Fetal Heart	heart
29	chr15:74019800-74020200	Weak transcription	Right Atrium	heart
30	chr15:74019800-74020200	Weak transcription	Right Ventricle	heart
31	chr15:74020000-74020800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
32	chr15:74020200-74020400	Enhancers	Right Atrium	heart
33	chr15:74020200-74020800	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
34	chr15:74020200-74021800	Enhancers	Right Ventricle	heart
35	chr15:74020400-74020600	Bivalent Enhancer	Stomach Smooth Muscle	stomach
36	chr15:74020400-74021400	Weak transcription	Right Atrium	heart
37	chr15:74021400-74021800	Enhancers	Right Atrium	heart
38	chr15:74021800-74033400	Weak transcription	Right Atrium	heart
39	chr15:74022000-74022200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
40	chr15:74022200-74028000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
41	chr15:74023400-74023600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
42	chr15:74023400-74023800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
43	chr15:74023600-74036400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
44	chr15:74023800-74024800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
45	chr15:74024800-74025400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
46	chr15:74025000-74025600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
47	chr15:74025200-74025600	Bivalent Enhancer	NHEK	skin
48	chr15:74025200-74025800	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
49	chr15:74025400-74025600	Enhancers	ES-I3 Cell Line	embryonic stem cell
50	chr15:74025400-74025600	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived

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