Variant report

Variant	esv3362898
Chromosome Location	chr15:58705732-58850860
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3201)
CpG islands
(count:1282)
Chromatin interactive
region (count:145)
LncRNA
region (count:12)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:3201 , 50 per page) page: 1 2 3 4 5 6 7 ... 65

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:58712314-58712545	HepG2	liver:	n/a	n/a
2	ARID3A	chr15:58812778-58814188	K562	blood:	n/a	n/a
3	ARID3A	chr15:58767778-58769308	HepG2	liver:	n/a	n/a
4	ARID3A	chr15:58749976-58750707	HepG2	liver:	n/a	n/a
5	ARID3A	chr15:58785240-58785433	K562	blood:	n/a	n/a
6	ARID3A	chr15:58838842-58839281	K562	blood:	n/a	n/a
7	ARID3A	chr15:58707734-58708189	K562	blood:	n/a	n/a
8	ARID3A	chr15:58722084-58722767	K562	blood:	n/a	n/a
9	ARID3A	chr15:58747156-58747675	HepG2	liver:	n/a	n/a
10	ARID3A	chr15:58717507-58717628	HepG2	liver:	n/a	n/a
11	ARID3A	chr15:58844004-58844144	K562	blood:	n/a	n/a
12	ARID3A	chr15:58843760-58844405	HepG2	liver:	n/a	n/a
13	ARID3A	chr15:58733286-58733314	K562	blood:	n/a	n/a
14	ARID3A	chr15:58723845-58724674	HepG2	liver:	n/a	n/a
15	ARID3A	chr15:58843627-58843679	K562	blood:	n/a	n/a
16	ARID3A	chr15:58820207-58820855	HepG2	liver:	n/a	n/a
17	ARID3A	chr15:58734368-58734618	HepG2	liver:	n/a	n/a
18	ARID3A	chr15:58761980-58762558	HepG2	liver:	n/a	n/a
19	ARID3A	chr15:58755905-58756780	HepG2	liver:	n/a	n/a
20	ARID3A	chr15:58731190-58731493	HepG2	liver:	n/a	n/a
21	ARID3A	chr15:58759096-58761393	HepG2	liver:	n/a	n/a
22	ATF1	chr15:58705605-58705761	K562	blood:	n/a	n/a
23	ATF1	chr15:58810309-58810725	K562	blood:	n/a	n/a
24	ATF1	chr15:58813645-58814435	K562	blood:	n/a	n/a
25	ATF1	chr15:58843838-58844224	K562	blood:	n/a	n/a
26	ATF1	chr15:58808004-58808383	K562	blood:	n/a	n/a
27	ATF1	chr15:58759466-58759852	K562	blood:	n/a	n/a
28	ATF1	chr15:58749705-58749952	K562	blood:	n/a	n/a
29	ATF1	chr15:58760148-58760226	K562	blood:	n/a	n/a
30	ATF1	chr15:58762340-58762460	K562	blood:	n/a	n/a
31	ATF1	chr15:58837601-58837928	K562	blood:	n/a	n/a
32	ATF1	chr15:58763625-58763852	K562	blood:	n/a	n/a
33	ATF1	chr15:58722141-58722665	K562	blood:	n/a	n/a
34	ATF1	chr15:58838759-58839354	K562	blood:	n/a	n/a
35	ATF2	chr15:58807930-58808408	GM12878	blood:	n/a	n/a
36	ATF2	chr15:58746536-58747070	GM12878	blood:	n/a	n/a
37	ATF2	chr15:58810025-58810912	GM12878	blood:	n/a	n/a
38	ATF2	chr15:58765953-58766459	GM12878	blood:	n/a	n/a
39	ATF2	chr15:58807914-58808407	GM12878	blood:	n/a	n/a
40	ATF2	chr15:58712602-58713391	GM12878	blood:	n/a	n/a
41	ATF2	chr15:58746518-58747031	GM12878	blood:	n/a	n/a
42	ATF2	chr15:58749604-58750667	GM12878	blood:	n/a	n/a
43	ATF2	chr15:58809964-58810730	GM12878	blood:	n/a	n/a
44	ATF2	chr15:58765955-58766385	GM12878	blood:	n/a	n/a
45	ATF2	chr15:58813644-58814121	GM12878	blood:	n/a	n/a
46	ATF2	chr15:58749559-58750757	GM12878	blood:	n/a	n/a
47	ATF3	chr15:58813620-58813978	K562	blood:	n/a	n/a
48	ATF3	chr15:58820176-58820772	A549	lung:	n/a	n/a
49	ATF3	chr15:58722156-58722424	K562	blood:	n/a	n/a
50	ATF3	chr15:58838821-58839124	K562	blood:	n/a	n/a

(count:1282 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:58782685-58782735	HCT-116	colon:	n/a
2	chr15:58782685-58782735	HCT-116	colon:	n/a
3	chr15:58844359-58844409	T-47D	breast:	n/a
4	chr15:58797839-58797889	MCF-7	breast:	n/a
5	chr15:58723879-58723929	GM19239	blood:	n/a
6	chr15:58766885-58766935	IMR90	lung:	fetal
7	chr15:58791257-58791307	IMR90	lung:	fetal
8	chr15:58724041-58724091	HAEpiC	amniotic membrane:	n/a
9	chr15:58782685-58782735	HPAEpiC	pulmonary alveolar:	n/a
10	chr15:58724225-58724275	A549	lung:	n/a
11	chr15:58733736-58733786	GM19239	blood:	n/a
12	chr15:58733736-58733786	GM12891	blood:	n/a
13	chr15:58797839-58797889	HRCEpiC	kidney:	n/a
14	chr15:58782685-58782735	H1-hESC	embryonic stem cell:	embryo
15	chr15:58782685-58782735	PrEC	prostate:	n/a
16	chr15:58840678-58840728	HRPEpiC	eye:	n/a
17	chr15:58766885-58766935	PANC-1	pancreas:	n/a
18	chr15:58797839-58797889	PFSK-1	brain:	n/a
19	chr15:58812960-58813010	SK-N-SH	brain:	n/a
20	chr15:58723851-58723901	AG09309	skin:	n/a
21	chr15:58723879-58723929	PANC-1	pancreas:	n/a
22	chr15:58839555-58839605	BJ	skin:	n/a
23	chr15:58844583-58844633	HUVEC	blood vessel:	n/a
24	chr15:58758468-58758518	HEK293	kidney:	embryo
25	chr15:58844359-58844409	HMEC	breast:	n/a
26	chr15:58844359-58844409	HPAEpiC	pulmonary alveolar:	n/a
27	chr15:58844583-58844633	HCM	heart:	n/a
28	chr15:58844583-58844633	T-47D	breast:	n/a
29	chr15:58791257-58791307	HPAEpiC	pulmonary alveolar:	n/a
30	chr15:58840678-58840728	AG09319	gingival:	n/a
31	chr15:58758468-58758518	AG04450	lung:	fetal
32	chr15:58724041-58724091	HCF	heart:	n/a
33	chr15:58844359-58844409	PFSK-1	brain:	n/a
34	chr15:58758468-58758518	HPAEpiC	pulmonary alveolar:	n/a
35	chr15:58812960-58813010	HCT-116	colon:	n/a
36	chr15:58723851-58723901	GM06990	blood:	n/a
37	chr15:58723851-58723901	RPTEC	kidney:	n/a
38	chr15:58812960-58813010	GM12891	blood:	n/a
39	chr15:58766885-58766935	AG09309	skin:	n/a
40	chr15:58723657-58723707	PrEC	prostate:	n/a
41	chr15:58840596-58840646	PrEC	prostate:	n/a
42	chr15:58723851-58723901	PFSK-1	brain:	n/a
43	chr15:58766885-58766935	HL-60	blood:	n/a
44	chr15:58791257-58791307	SAEC	small airway:	n/a
45	chr15:58840596-58840646	BE2_C	brain:	n/a
46	chr15:58844583-58844633	H1-hESC	embryonic stem cell:	embryo
47	chr15:58812960-58813010	HAEpiC	amniotic membrane:	n/a
48	chr15:58723851-58723901	HRPEpiC	eye:	n/a
49	chr15:58723851-58723901	AoSMC	blood vessel:	n/a
50	chr15:58812960-58813010	AG04450	lung:	fetal

(count:145 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr15:58816638..58820223-chr15:58821126..58823355,3	K562	blood:
2	chr15:58818144..58821107-chr15:58827941..58830725,2	K562	blood:
3	chr15:58750305..58752654-chr15:58755983..58757859,3	K562	blood:
4	chr15:58797460..58800451-chr15:58803881..58805523,2	K562	blood:
5	chr15:58767133..58770014-chr15:58770584..58772843,2	MCF-7	breast:
6	chr15:58623609..58625282-chr15:58727962..58730632,2	MCF-7	breast:
7	chr15:58742210..58745056-chr15:58745443..58748993,3	K562	blood:
8	chr15:58844000..58845908-chr15:58853129..58855286,2	K562	blood:
9	chr15:58814045..58816618-chr15:58898707..58900922,2	MCF-7	breast:
10	chr15:58811000..58814506-chr15:58833587..58836863,3	K562	blood:
11	chr15:58821255..58823179-chr15:58836509..58838748,2	K562	blood:
12	chr15:58720668..58723820-chr15:58759148..58762580,3	K562	blood:
13	chr15:58841313..58844294-chr15:58848370..58850226,2	K562	blood:
14	chr15:58805398..58807499-chr15:58809534..58812404,4	MCF-7	breast:
15	chr15:58836656..58842196-chr15:58843431..58849915,8	K562	blood:
16	chr15:58811000..58814506-chr15:58833587..58836863,3	K562	blood:
17	chr15:58765282..58766825-chr15:58783128..58785341,2	K562	blood:
18	chr15:58790757..58793256-chr15:58794935..58797026,2	K562	blood:
19	chr15:58742210..58745056-chr15:58745443..58748993,3	K562	blood:
20	chr15:58812575..58815325-chr15:58843755..58846624,5	K562	blood:
21	chr15:58800980..58802725-chr15:58817478..58819244,2	K562	blood:
22	chr15:58623889..58626326-chr15:58704441..58709164,4	K562	blood:
23	chr15:58723370..58725024-chr15:58732776..58734366,2	K562	blood:
24	chr15:58726654..58728474-chr15:58730449..58733344,2	MCF-7	breast:
25	chr15:58800669..58805424-chr15:58807712..58810883,4	K562	blood:
26	chr15:58810857..58816650-chr15:58835363..58842392,10	K562	blood:
27	chr15:58762234..58763977-chr15:59040711..59042531,2	K562	blood:
28	chr15:58731963..58734945-chr15:58743116..58746394,3	K562	blood:
29	chr15:58762574..58764554-chr15:58812167..58813777,2	K562	blood:
30	chr15:58824835..58829265-chr15:58838025..58840916,4	K562	blood:
31	chr15:58838134..58839678-chr15:58847125..58849690,2	K562	blood:
32	chr15:58731261..58732919-chr15:58735065..58738026,2	K562	blood:
33	chr15:58791633..58793802-chr15:58794935..58797234,3	K562	blood:
34	chr15:58797035..58800948-chr15:58803702..58808140,4	K562	blood:
35	chr15:58815750..58818981-chr15:58825032..58827694,3	K562	blood:
36	chr15:58767751..58769658-chr15:58771265..58773299,2	MCF-7	breast:
37	chr15:58728810..58730578-chr15:58760180..58761799,2	MCF-7	breast:
38	chr15:58778802..58780678-chr15:58783257..58786951,3	K562	blood:
39	chr15:58769989..58771899-chr15:58773674..58776005,2	K562	blood:
40	chr15:58706598..58709949-chr15:58711625..58715312,3	K562	blood:
41	chr15:58754820..58757599-chr15:58758355..58762013,3	K562	blood:
42	chr15:58814659..58816490-chr15:58819397..58821413,2	MCF-7	breast:
43	chr15:58623562..58626994-chr15:58730618..58733502,3	MCF-7	breast:
44	chr15:58709732..58712579-chr15:58730855..58732681,2	K562	blood:
45	chr15:58800980..58802725-chr15:58817478..58819244,2	K562	blood:
46	chr15:58815957..58817851-chr15:58819397..58821378,2	MCF-7	breast:
47	chr15:58726222..58728488-chr15:58751000..58752953,2	K562	blood:
48	chr15:58730817..58731598-chr22:22510997..22511880,2	HCT-116	colon:
49	chr15:58545760..58547993-chr15:58842385..58845023,2	MCF-7	breast:
50	chr15:58728810..58730578-chr15:58760180..58761799,2	MCF-7	breast:

(count:12 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ADAM10-9	chr15:58765830-58765959	NONHSAT044093
2	lnc-ALDH1A2-1	chr15:58727089-58729111	ENSG00000259293.1
3	lnc-FAM63B-2	chr15:58814150-58815568	ENSG00000249011
4	lnc-AQP9-5	chr15:58724192-58724562	NONHSAT044110
5	lnc-ALDH1A2-1	chr15:58786972-58787082	ENSG00000259293.1
6	lnc-FAM63B-2	chr15:58814150-58815570	ENSG00000259476.1
7	lnc-ADAM10-9	chr15:58789916-58790065	NONHSAT044093
8	lnc-ADAM10-9	chr15:58712170-58712304	NONHSAT044093
9	lnc-AQP9-5	chr15:58723026-58723350	NONHSAT044110
10	lnc-FAM63B-2	chr15:58813510-58813845	ENSG00000249011
11	lnc-FAM63B-2	chr15:58813510-58813845	ENSG00000259476.1
12	lnc-ALDH1A2-1	chr15:58790838-58790934	ENSG00000259293.1

No data

Variant related genes	Relation type
LIPC	TF binding region
ENSG00000259476	TF binding region
ENSG00000259293	TF binding region
ALDH1A2	TF binding region
LIPC	CpG island
ENSG00000259476	CpG island
ENSG00000259293	CpG island
ALDH1A2	CpG island
ENSG00000233720	chromatin interactions
ENSG00000137845	chromatin interactions
ENSG00000166035	chromatin interactions
ENSG00000128918	chromatin interactions
ENSG00000259293	chromatin interactions
ENSG00000137776	chromatin interactions
ENSG00000259476	chromatin interactions
RAB14	miRNA target sites

Extended variants
information (count: 6565 )
Associated
traits (count: 63 )

Variant overlapped rSNPs/rCNVs (count:6565 , 50 per page) page: 1 2 3 4 5 6 7 ... 132

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs548087682	chr15:58705741-58705742	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs72740857	chr15:58705744-58705745	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs183693565	chr15:58705763-58705764	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs117463013	chr15:58705805-58705806	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs570205049	chr15:58705832-58705833	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs539033222	chr15:58705854-58705855	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs558944157	chr15:58705869-58705870	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs566087266	chr15:58705874-58705875	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs72740858	chr15:58705943-58705944	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs62000868	chr15:58705980-58705981	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs528927784	chr15:58705981-58705982	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs189076247	chr15:58705988-58705989	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs548681501	chr15:58705995-58705996	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs542002671	chr15:58706048-58706049	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs556769683	chr15:58706055-58706056	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs376044547	chr15:58706115-58706116	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs545504825	chr15:58706119-58706120	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs558891563	chr15:58706131-58706132	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs117346975	chr15:58706167-58706168	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs541342048	chr15:58706195-58706196	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs561661359	chr15:58706225-58706226	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs192178079	chr15:58706237-58706238	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs550398383	chr15:58706244-58706245	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs142061843	chr15:58706265-58706266	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs35096874	chr15:58706289-58706290	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs571559652	chr15:58706315-58706316	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs533734770	chr15:58706335-58706336	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs556902521	chr15:58706438-58706439	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs566050546	chr15:58706457-58706458	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs146317951	chr15:58706464-58706465	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs184447649	chr15:58706506-58706507	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs201732075	chr15:58706513-58706514	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs568382296	chr15:58706524-58706525	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs189371437	chr15:58706659-58706660	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs191593419	chr15:58706661-58706662	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs576644547	chr15:58706696-58706697	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs184113834	chr15:58706698-58706699	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs188810500	chr15:58706719-58706720	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs76137124	chr15:58706732-58706733	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs573778970	chr15:58706752-58706753	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs12916206	chr15:58706797-58706798	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs560294406	chr15:58706800-58706801	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs556705687	chr15:58706814-58706815	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs181611413	chr15:58706825-58706826	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs414846	chr15:58706846-58706847	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs563836781	chr15:58706850-58706851	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs532775192	chr15:58706872-58706873	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs552680914	chr15:58706873-58706874	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs186990200	chr15:58706897-58706898	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs118151833	chr15:58706904-58706905	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:63)

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
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
Chronic lymphocytic leukemia	21546498	CNVD
Congenital diaphragmatic hernia	21341218	CNVD
Holoprosencephaly	21359414	CNVD
Myelofibrosis	22110671	CNVD
Adenocarcinoma	19607727	CNVD
Squamous cell cancer	19607727	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Melanoma	20877625	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:3319 , 50 per page) page: 1 2 3 4 5 6 7 ... 67

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:58694800-58716000	Weak transcription	Esophagus	oesophagus
2	chr15:58703000-58712800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
3	chr15:58703400-58707600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
4	chr15:58703400-58718600	Weak transcription	Primary T cells from cord blood	blood
5	chr15:58704600-58728800	Weak transcription	Thymus	Thymus
6	chr15:58704800-58711200	Weak transcription	Liver	Liver
7	chr15:58705000-58707600	Weak transcription	Dnd41	blood
8	chr15:58705400-58705800	Enhancers	K562	blood
9	chr15:58705600-58705800	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr15:58705800-58707800	Weak transcription	K562	blood
11	chr15:58707600-58708000	Enhancers	Dnd41	blood
12	chr15:58707600-58708400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
13	chr15:58707800-58708000	Enhancers	K562	blood
14	chr15:58711000-58712400	Enhancers	GM12878-XiMat	blood
15	chr15:58711200-58711400	Enhancers	Liver	Liver
16	chr15:58711400-58711600	Enhancers	Placenta	Placenta
17	chr15:58711400-58711800	Weak transcription	Liver	Liver
18	chr15:58711400-58716200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
19	chr15:58711600-58712400	Weak transcription	Placenta	Placenta
20	chr15:58711800-58722000	Enhancers	Liver	Liver
21	chr15:58712000-58712200	Active TSS	HepG2	liver
22	chr15:58712200-58712400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
23	chr15:58712200-58712600	Flanking Active TSS	HepG2	liver
24	chr15:58712200-58713000	Enhancers	K562	blood
25	chr15:58712200-58713800	Enhancers	A549	lung
26	chr15:58712400-58712800	Flanking Active TSS	GM12878-XiMat	blood
27	chr15:58712400-58713000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
28	chr15:58712400-58713200	Enhancers	Placenta	Placenta
29	chr15:58712600-58712800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
30	chr15:58712600-58713200	Enhancers	HepG2	liver
31	chr15:58712800-58713200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
32	chr15:58712800-58714200	Enhancers	GM12878-XiMat	blood
33	chr15:58712800-58718600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
34	chr15:58713000-58713200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
35	chr15:58713000-58713200	Enhancers	Fetal Muscle Trunk	muscle
36	chr15:58713000-58716200	Weak transcription	K562	blood
37	chr15:58713200-58715400	Weak transcription	HepG2	liver
38	chr15:58713200-58716200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
39	chr15:58713800-58716000	Weak transcription	A549	lung
40	chr15:58714200-58714400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
41	chr15:58714200-58716200	Weak transcription	GM12878-XiMat	blood
42	chr15:58714800-58716000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
43	chr15:58715000-58718000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
44	chr15:58715200-58716400	Enhancers	NHDF-Ad	bronchial
45	chr15:58715400-58716000	Enhancers	HepG2	liver
46	chr15:58715400-58717800	Enhancers	Duodenum Mucosa	Duodenum
47	chr15:58715800-58716600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
48	chr15:58716000-58716600	Enhancers	Muscle Satellite Cultured Cells	--
49	chr15:58716000-58716600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
50	chr15:58716000-58716600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin

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