Variant report

Variant	nsv833010
Chromosome Location	chr15:53935652-54099849
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:595)
CpG islands
(count:610)
Chromatin interactive
region (count:38)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:595 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:54009147-54009455	HepG2	liver:	n/a	n/a
2	ARID3A	chr15:53958161-53958371	HepG2	liver:	n/a	n/a
3	ARID3A	chr15:53947832-53947856	HepG2	liver:	n/a	n/a
4	ARID3A	chr15:54039721-54040249	HepG2	liver:	n/a	n/a
5	BACH1	chr15:54009217-54009423	H1-hESC	embryonic stem cell:	n/a	n/a
6	CEBPB	chr15:54059407-54059749	HepG2	liver:	n/a	chr15:54059574-54059585
7	CEBPB	chr15:53971315-53971562	A549	lung:	n/a	chr15:53971439-53971450
8	CEBPB	chr15:54063126-54063389	A549	lung:	n/a	chr15:54063268-54063279
9	CEBPB	chr15:54078654-54078952	HepG2	liver:	n/a	chr15:54078793-54078804
10	CEBPB	chr15:54059452-54059670	A549	lung:	n/a	chr15:54059574-54059585
11	CEBPB	chr15:54063100-54063415	HepG2	liver:	n/a	chr15:54063268-54063279
12	CEBPB	chr15:54080501-54080573	A549	lung:	n/a	chr15:54080531-54080544
13	CEBPB	chr15:53971377-53971565	HepG2	liver:	n/a	chr15:53971439-53971450
14	CEBPB	chr15:54063214-54063311	H1-hESC	embryonic stem cell:	n/a	chr15:54063268-54063279
15	CEBPB	chr15:54075082-54075175	K562	blood:	n/a	n/a
16	CHD1	chr15:53947735-53947742	H1-hESC	embryonic stem cell:	n/a	n/a
17	CHD2	chr15:54048368-54048478	K562	blood:	n/a	n/a
18	CHD2	chr15:54047971-54048070	H1-hESC	embryonic stem cell:	n/a	n/a
19	CHD2	chr15:54051550-54051728	H1-hESC	embryonic stem cell:	n/a	n/a
20	CHD2	chr15:54048319-54048477	H1-hESC	embryonic stem cell:	n/a	n/a
21	CTCF	chr15:53958200-53958350	SAEC	small airway:	n/a	chr15:53958293-53958314 chr15:53958298-53958316
22	CTCF	chr15:54009220-54009370	HepG2	liver:	n/a	chr15:54009305-54009323 chr15:54009300-54009321
23	CTCF	chr15:54009780-54009930	HUVEC	blood vessel:	n/a	n/a
24	CTCF	chr15:54009540-54009690	HMEC	breast:	n/a	n/a
25	CTCF	chr15:54009820-54009970	HA-sp	spinal cord:	n/a	n/a
26	CTCF	chr15:53958260-53958410	WERI-Rb-1	eye:	n/a	chr15:53958293-53958314 chr15:53958298-53958316
27	CTCF	chr15:54009220-54009370	HA-sp	spinal cord:	n/a	chr15:54009305-54009323 chr15:54009300-54009321
28	CTCF	chr15:53947680-53947830	A549	lung:	n/a	n/a
29	CTCF	chr15:53987960-53988110	MCF-7	breast:	n/a	n/a
30	CTCF	chr15:54009160-54009408	MCF-7	breast:	n/a	chr15:54009305-54009323 chr15:54009300-54009321
31	CTCF	chr15:53958240-53958390	HMF	breast:	n/a	chr15:53958293-53958314 chr15:53958298-53958316
32	CTCF	chr15:53947761-53947929	LNCaP	prostate:	n/a	n/a
33	CTCF	chr15:54009800-54009950	HCPEpiC	choroid plexus:	n/a	n/a
34	CTCF	chr15:53958289-53958337	Spleen_OC	spleen:	n/a	chr15:53958293-53958314 chr15:53958298-53958316
35	CTCF	chr15:54009147-54009473	A549	lung:	n/a	chr15:54009305-54009323 chr15:54009300-54009321
36	CTCF	chr15:53947740-53947890	RPTEC	kidney:	n/a	n/a
37	CTCF	chr15:54009000-54009150	NHEK	skin:	n/a	n/a
38	CTCF	chr15:54095780-54095930	RPTEC	kidney:	n/a	n/a
39	CTCF	chr15:53958260-53958410	HMEC	breast:	n/a	chr15:53958293-53958314 chr15:53958298-53958316
40	CTCF	chr15:54009249-54009375	GM10248	blood:	n/a	chr15:54009305-54009323 chr15:54009300-54009321
41	CTCF	chr15:54009780-54009930	HepG2	liver:	n/a	n/a
42	CTCF	chr15:54009800-54009950	HepG2	liver:	n/a	n/a
43	CTCF	chr15:54009123-54009522	GM12878	blood:	n/a	chr15:54009305-54009323 chr15:54009300-54009321
44	CTCF	chr15:53947820-53947970	SK-N-SH_RA	brain:	n/a	n/a
45	CTCF	chr15:54009740-54009890	GM12878	blood:	n/a	n/a
46	CTCF	chr15:54009820-54009970	WERI-Rb-1	eye:	n/a	n/a
47	CTCF	chr15:53958231-53958440	MCF-7	breast:	n/a	chr15:53958293-53958314 chr15:53958298-53958316
48	CTCF	chr15:54009187-54009450	Medullo	brain:	n/a	chr15:54009305-54009323 chr15:54009300-54009321
49	CTCF	chr15:53946372-53946415	Medullo	brain:	n/a	n/a
50	CTCF	chr15:53958200-53958350	SK-N-SH_RA	brain:	n/a	chr15:53958293-53958314 chr15:53958298-53958316

(count:610 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:54055336-54055386	AG04449	skin:	fetal
2	chr15:54051543-54051593	HIPEpiC	eye:	n/a
3	chr15:54051543-54051593	MCF10A-Er-Src	breast:	n/a
4	chr15:53943590-53943640	HNPCEpiC	eye:	n/a
5	chr15:54051239-54051289	GM06990	blood:	n/a
6	chr15:54051747-54051797	HPAEpiC	pulmonary alveolar:	n/a
7	chr15:54051239-54051289	HCT-116	colon:	n/a
8	chr15:54051901-54051951	Jurkat	blood:	n/a
9	chr15:54051901-54051951	HMEC	breast:	n/a
10	chr15:54049269-54049319	ECC-1	luminal epithelium:	n/a
11	chr15:54049269-54049319	HAEpiC	amniotic membrane:	n/a
12	chr15:54051880-54051930	A549	lung:	n/a
13	chr15:54052740-54052790	LNCaP	prostate:	n/a
14	chr15:54051239-54051289	SK-N-SH_RA	brain:	n/a
15	chr15:54049269-54049319	HCPEpiC	choroid plexus:	n/a
16	chr15:54051747-54051797	HNPCEpiC	eye:	n/a
17	chr15:54051901-54051951	MCF-7	breast:	n/a
18	chr15:53943590-53943640	Jurkat	blood:	n/a
19	chr15:53943590-53943640	SAEC	small airway:	n/a
20	chr15:54052305-54052355	MCF10A-Er-Src	breast:	n/a
21	chr15:54052740-54052790	HCF	heart:	n/a
22	chr15:54051239-54051289	SK-N-SH	brain:	n/a
23	chr15:54055336-54055386	NT2-D1	testis:	n/a
24	chr15:54052740-54052790	Hela-S3	cervix:	n/a
25	chr15:54049269-54049319	HEK293	kidney:	embryo
26	chr15:53943590-53943640	AG09319	gingival:	n/a
27	chr15:54051880-54051930	HCF	heart:	n/a
28	chr15:54051239-54051289	HMEC	breast:	n/a
29	chr15:54055336-54055386	HCF	heart:	n/a
30	chr15:53943590-53943640	AG04449	skin:	fetal
31	chr15:54051880-54051930	SK-N-SH	brain:	n/a
32	chr15:53943590-53943640	AG09309	skin:	n/a
33	chr15:54052305-54052355	AG09319	gingival:	n/a
34	chr15:54051880-54051930	NT2-D1	testis:	n/a
35	chr15:54052305-54052355	AoSMC	blood vessel:	n/a
36	chr15:54051880-54051930	K562	blood:	n/a
37	chr15:54052740-54052790	GM06990	blood:	n/a
38	chr15:54051747-54051797	AG04449	skin:	fetal
39	chr15:54051543-54051593	MCF-7	breast:	n/a
40	chr15:54052305-54052355	LNCaP	prostate:	n/a
41	chr15:54051901-54051951	HCF	heart:	n/a
42	chr15:54051543-54051593	PFSK-1	brain:	n/a
43	chr15:54051747-54051797	SK-N-MC	brain:	n/a
44	chr15:54051901-54051951	AG04449	skin:	fetal
45	chr15:54051543-54051593	ovcar-3	ovarian:	n/a
46	chr15:54049269-54049319	A549	lung:	n/a
47	chr15:54052740-54052790	AG09309	skin:	n/a
48	chr15:54051880-54051930	ovcar-3	ovarian:	n/a
49	chr15:54052305-54052355	HUVEC	blood vessel:	n/a
50	chr15:54051543-54051593	RPTEC	kidney:	n/a

(count:38 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:54025883..54029184-chr15:54031386..54034833,4	MCF-7	breast:
2	chr15:53057704..53058252-chr15:53950484..53951446,2	MCF-7	breast:
3	chr15:53958809..53961070-chr15:53966400..53969207,2	MCF-7	breast:
4	chr15:54050503..54054059-chr15:54055807..54059339,3	MCF-7	breast:
5	chr15:53252582..53253162-chr15:54009367..54009914,2	MCF-7	breast:
6	chr15:53072253..53073288-chr15:54008890..54009735,3	MCF-7	breast:
7	chr15:54077990..54080956-chr15:54224851..54227112,2	MCF-7	breast:
8	chr15:53057663..53058643-chr15:53947402..53948111,2	MCF-7	breast:
9	chr15:53072550..53073539-chr15:53947412..53948347,3	MCF-7	breast:
10	chr15:54025883..54029184-chr15:54031386..54034833,4	MCF-7	breast:
11	chr15:53072398..53073448-chr15:54008592..54010016,9	MCF-7	breast:
12	chr15:54034974..54037119-chr15:54039892..54041894,2	MCF-7	breast:
13	chr15:53984291..53986517-chr15:53987767..53990202,2	MCF-7	breast:
14	chr15:54050503..54054059-chr15:54055807..54059339,3	MCF-7	breast:
15	chr15:54034974..54037119-chr15:54039892..54041894,2	MCF-7	breast:
16	chr15:53949957..53952071-chr15:53952352..53954072,2	MCF-7	breast:
17	chr12:2392202..2393702-chr15:54036267..54038499,2	MCF-7	breast:
18	chr15:54023576..54026750-chr15:54026892..54029549,4	MCF-7	breast:
19	chr15:54031475..54033401-chr15:54036496..54038741,2	MCF-7	breast:
20	chr15:52586498..52588343-chr15:54006889..54008780,2	MCF-7	breast:
21	chr15:53945998..53946891-chr15:54009249..54010202,2	MCF-7	breast:
22	chr15:54035259..54036883-chr15:54037384..54039611,2	MCF-7	breast:
23	chr15:53676303..53677625-chr15:54008801..54010344,5	MCF-7	breast:
24	chr15:53949957..53952071-chr15:53952352..53954072,2	MCF-7	breast:
25	chr15:53676366..53677226-chr15:53947378..53948497,3	MCF-7	breast:
26	chr15:53489257..53489939-chr15:54008536..54009320,2	MCF-7	breast:
27	chr15:54035259..54036883-chr15:54037384..54039611,2	MCF-7	breast:
28	chr15:54005385..54005905-chr17:46955446..46956217,3	MCF-7	breast:
29	chr15:53984291..53986517-chr15:53987767..53990202,2	MCF-7	breast:
30	chr15:54082466..54084805-chr15:54086509..54088980,2	K562	blood:
31	chr15:53945998..53946891-chr15:54009249..54010202,2	MCF-7	breast:
32	chr15:53072427..53073417-chr15:53957937..53958702,5	MCF-7	breast:
33	chr15:53057943..53058467-chr15:54010298..54010948,2	MCF-7	breast:
34	chr15:53676762..53677326-chr15:53957733..53958557,2	MCF-7	breast:
35	chr15:54031475..54033401-chr15:54036496..54038741,2	MCF-7	breast:
36	chr15:53958809..53961070-chr15:53966400..53969207,2	MCF-7	breast:
37	chr15:54082466..54084805-chr15:54086509..54088980,2	K562	blood:
38	chr12:86243212..86244125-chr15:53990318..53991124,2	MCF-7	breast:

No data

Variant related genes	Relation type
RNU2-53P	TF binding region
RNU6-449P	TF binding region
WDR72	TF binding region
RNU2-53P	CpG island
RNU6-449P	CpG island
WDR72	CpG island
ENSG00000169856	chromatin interactions
ENSG00000206641	chromatin interactions
ENSG00000128833	chromatin interactions
ENSG00000166415	chromatin interactions

Extended variants
information (count: 5286 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:5286 , 50 per page) page: 1 2 3 4 5 6 7 ... 106

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs187471802	chr15:53935676-53935677	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs529822252	chr15:53935687-53935688	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs548381572	chr15:53935745-53935746	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs115318793	chr15:53935771-53935772	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs562835597	chr15:53935798-53935799	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs146858642	chr15:53935836-53935837	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs526055	chr15:53935857-53935858	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs34731937	chr15:53935870-53935871	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs565513756	chr15:53935882-53935883	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs114851494	chr15:53935883-53935884	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs547821184	chr15:53935890-53935891	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs567950460	chr15:53935891-53935892	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs536511807	chr15:53935916-53935917	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs548592054	chr15:53935921-53935922	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs568492010	chr15:53935929-53935930	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs143473184	chr15:53935930-53935931	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs371650637	chr15:53935931-53935932	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs557424889	chr15:53935934-53935935	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs577465535	chr15:53935935-53935936	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs533996595	chr15:53935943-53935944	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs192964692	chr15:53935991-53935992	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs573893342	chr15:53935992-53935993	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs200886121	chr15:53936025-53936026	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs184791096	chr15:53936026-53936027	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs189600376	chr15:53936090-53936091	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs367713311	chr15:53936118-53936119	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs533843570	chr15:53936149-53936150	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs553880941	chr15:53936211-53936212	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs576486329	chr15:53936213-53936214	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs192516335	chr15:53936286-53936287	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs117443561	chr15:53936288-53936289	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs527736318	chr15:53936289-53936290	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs547978231	chr15:53936300-53936301	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs140660845	chr15:53936323-53936324	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs72747350	chr15:53936362-53936363	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs62005953	chr15:53936378-53936379	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs10518731	chr15:53936418-53936419	Weak transcription Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs145743992	chr15:53936453-53936454	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
39	rs183606752	chr15:53936506-53936507	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
40	rs117935499	chr15:53936535-53936536	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
41	rs571330755	chr15:53936557-53936558	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
42	rs200027552	chr15:53936578-53936579	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
43	rs2675328	chr15:53936627-53936628	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs77497881	chr15:53936628-53936629	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs564399965	chr15:53936734-53936735	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs368577456	chr15:53936735-53936736	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs567325296	chr15:53936752-53936753	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs372495280	chr15:53936765-53936766	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs74015846	chr15:53936785-53936786	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs79996920	chr15:53936795-53936796	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:65)

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
Breast cancer	22032731	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
Esophageal adenocarcinoma	18820669	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Myelofibrosis	22110671	CNVD
Acute monocytic leukemia	16498392	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Breast cancer	17133270	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
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:375 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:53927200-53951400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr15:53927600-53941200	Weak transcription	Liver	Liver
3	chr15:53936400-53936600	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
4	chr15:53936600-53936800	Enhancers	iPS-20b Cell Line	embryonic stem cell
5	chr15:53936600-53937200	Enhancers	HUES64 Cell Line	embryonic stem cell
6	chr15:53936800-53937000	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
7	chr15:53936800-53937200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr15:53936800-53937200	Enhancers	HUES6 Cell Line	embryonic stem cell
9	chr15:53936800-53937400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr15:53936800-53937400	Enhancers	HUES48 Cell Line	embryonic stem cell
11	chr15:53937000-53937600	Enhancers	iPS-18 Cell Line	embryonic stem cell
12	chr15:53937000-53937600	Enhancers	iPS-20b Cell Line	embryonic stem cell
13	chr15:53941200-53943400	Enhancers	Liver	Liver
14	chr15:53943400-53953000	Weak transcription	Liver	Liver
15	chr15:53948800-53949000	Enhancers	Pancreatic Islets	Pancreatic Islet
16	chr15:53949000-53950800	Weak transcription	Pancreatic Islets	Pancreatic Islet
17	chr15:53949800-53951200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
18	chr15:53950000-53950200	Bivalent Enhancer	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr15:53950000-53951800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
20	chr15:53950200-53951600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr15:53950400-53951600	Enhancers	ES-I3 Cell Line	embryonic stem cell
22	chr15:53950400-53951800	Enhancers	Cortex derived primary cultured neurospheres	brain
23	chr15:53950600-53950800	Enhancers	Pancreas	Pancrea
24	chr15:53950600-53951200	Enhancers	Brain Germinal Matrix	brain
25	chr15:53950600-53951400	Enhancers	HepG2	liver
26	chr15:53950600-53951800	Enhancers	Fetal Heart	heart
27	chr15:53950600-53951800	Enhancers	Fetal Lung	lung
28	chr15:53950800-53951200	Enhancers	Pancreatic Islets	Pancreatic Islet
29	chr15:53950800-53951400	Enhancers	iPS-18 Cell Line	embryonic stem cell
30	chr15:53950800-53951800	Enhancers	HUES64 Cell Line	embryonic stem cell
31	chr15:53951000-53951800	Enhancers	HUES6 Cell Line	embryonic stem cell
32	chr15:53951000-53951800	Enhancers	iPS-15b Cell Line	embryonic stem cell
33	chr15:53951000-53951800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
34	chr15:53951200-53951600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr15:53951200-53951600	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
36	chr15:53951200-53951800	Enhancers	HUES48 Cell Line	embryonic stem cell
37	chr15:53951400-53951600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
38	chr15:53951400-53959200	Weak transcription	HepG2	liver
39	chr15:53951600-53951800	Bivalent Enhancer	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr15:53951600-53951800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
41	chr15:53951600-53973000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
42	chr15:53953000-53953600	Strong transcription	Liver	Liver
43	chr15:53953600-53955400	Weak transcription	Liver	Liver
44	chr15:53955400-53957800	Strong transcription	Liver	Liver
45	chr15:53957800-53972800	Weak transcription	Liver	Liver
46	chr15:53958000-53958600	Enhancers	Cortex derived primary cultured neurospheres	brain
47	chr15:53959200-53959600	Enhancers	HepG2	liver
48	chr15:53959400-53959600	Enhancers	Pancreas	Pancrea
49	chr15:53959600-53986200	Weak transcription	Pancreas	Pancrea
50	chr15:53961400-53961600	Bivalent Enhancer	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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