Variant report

Variant	nsv569433
Chromosome Location	chr15:53828686-53860607
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:104)
CpG islands
(count:122)
Chromatin interactive
region (count:14)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:104 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr15:53832081-53832492	MCF-7	breast:	n/a	chr15:53832239-53832250
2	CEBPB	chr15:53843464-53843609	A549	lung:	n/a	n/a
3	CEBPB	chr15:53849568-53849896	HepG2	liver:	n/a	n/a
4	CEBPB	chr15:53832063-53832437	A549	lung:	n/a	chr15:53832239-53832250
5	CEBPB	chr15:53832287-53832298	K562	blood:	n/a	n/a
6	CEBPB	chr15:53851707-53852190	HepG2	liver:	n/a	chr15:53852018-53852029
7	CEBPB	chr15:53831943-53832610	HCT-116	colon:	n/a	chr15:53832239-53832250
8	CEBPB	chr15:53832099-53832417	Hela-S3	cervix:	n/a	chr15:53832239-53832250
9	CEBPB	chr15:53832071-53832432	HepG2	liver:	n/a	chr15:53832239-53832250
10	CEBPB	chr15:53831896-53832561	A549	lung:	n/a	chr15:53832239-53832250
11	CEBPB	chr15:53832089-53832461	A549	lung:	n/a	chr15:53832239-53832250
12	CEBPB	chr15:53849559-53849894	A549	lung:	n/a	n/a
13	CEBPB	chr15:53832106-53832381	H1-hESC	embryonic stem cell:	n/a	chr15:53832239-53832250
14	CEBPB	chr15:53832070-53832380	IMR90	lung:	n/a	chr15:53832239-53832250
15	CEBPB	chr15:53849587-53849868	IMR90	lung:	n/a	n/a
16	CTCF	chr15:53837779-53837814	Kidney_OC	kidney:	n/a	n/a
17	CTCF	chr15:53852420-53852570	GM12864	blood:	n/a	n/a
18	ELF1	chr15:53842003-53842485	MCF-7	breast:	n/a	chr15:53842213-53842222
19	EP300	chr15:53851427-53852114	HepG2	liver:	n/a	chr15:53851928-53851942
20	EP300	chr15:53828394-53829241	A549	lung:	n/a	chr15:53828594-53828608 chr15:53828415-53828429 chr15:53828420-53828434
21	EP300	chr15:53828567-53829214	A549	lung:	n/a	chr15:53828594-53828608
22	EP300	chr15:53832332-53832442	K562	blood:	n/a	n/a
23	EP300	chr15:53832241-53832309	Hela-S3	cervix:	n/a	n/a
24	EP300	chr15:53851443-53852021	HepG2	liver:	n/a	chr15:53851928-53851942
25	FOS	chr15:53832137-53832424	MCF10A-Er-Src	breast:	n/a	n/a
26	FOS	chr15:53832123-53832400	MCF10A-Er-Src	breast:	n/a	n/a
27	FOSL2	chr15:53828514-53829183	A549	lung:	n/a	n/a
28	FOXA1	chr15:53842063-53842453	T-47D	breast:	n/a	n/a
29	FOXA1	chr15:53851497-53852005	HepG2	liver:	n/a	n/a
30	FOXA1	chr15:53851613-53852047	HepG2	liver:	n/a	n/a
31	FOXA1	chr15:53842137-53842381	T-47D	breast:	n/a	n/a
32	FOXA1	chr15:53851553-53852044	HepG2	liver:	n/a	n/a
33	FOXA1	chr15:53833135-53833433	HepG2	liver:	n/a	n/a
34	FOXA1	chr15:53840821-53841210	HepG2	liver:	n/a	n/a
35	FOXA2	chr15:53851587-53851909	HepG2	liver:	n/a	n/a
36	FOXA2	chr15:53833150-53833409	A549	lung:	n/a	n/a
37	FOXA2	chr15:53832962-53833532	A549	lung:	n/a	n/a
38	FOXA2	chr15:53828598-53829070	A549	lung:	n/a	n/a
39	HDAC2	chr15:53851574-53851936	HepG2	liver:	n/a	n/a
40	JUND	chr15:53847194-53847214	HepG2	liver:	n/a	n/a
41	MAFF	chr15:53850613-53850949	HepG2	liver:	n/a	chr15:53850766-53850784
42	MAFF	chr15:53856904-53857191	HepG2	liver:	n/a	n/a
43	MAFF	chr15:53858467-53858703	HepG2	liver:	n/a	n/a
44	MAFF	chr15:53850643-53850891	K562	blood:	n/a	chr15:53850766-53850784
45	MAFK	chr15:53858488-53858766	HepG2	liver:	n/a	chr15:53858612-53858627
46	MAFK	chr15:53850741-53850871	Hela-S3	cervix:	n/a	chr15:53850771-53850787 chr15:53850767-53850781 chr15:53850772-53850786 chr15:53850769-53850789 chr15:53850768-53850783 chr15:53850769-53850780
47	MAFK	chr15:53850598-53850958	HepG2	liver:	n/a	chr15:53850771-53850787 chr15:53850767-53850781 chr15:53850772-53850786 chr15:53850769-53850789 chr15:53850768-53850783 chr15:53850769-53850780
48	MAFK	chr15:53856888-53857196	IMR90	lung:	n/a	n/a
49	MAFK	chr15:53850615-53850942	HepG2	liver:	n/a	chr15:53850771-53850787 chr15:53850767-53850781 chr15:53850772-53850786 chr15:53850769-53850789 chr15:53850768-53850783 chr15:53850769-53850780
50	MAFK	chr15:53856872-53857205	HepG2	liver:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:53841455-53841505	ProgFib	skin:	n/a
2	chr15:53841455-53841505	NH-A	brain:	n/a
3	chr15:53841455-53841505	HEK293	kidney:	embryo
4	chr15:53852614-53852664	BJ	skin:	n/a
5	chr15:53852614-53852664	Hepatocyte	liver:	n/a
6	chr15:53852614-53852664	GM12892	blood:	n/a
7	chr15:53841455-53841505	HEEpiC	esophagus:	n/a
8	chr15:53852614-53852664	GM06990	blood:	n/a
9	chr15:53841455-53841505	GM19239	blood:	n/a
10	chr15:53841455-53841505	IMR90	lung:	fetal
11	chr15:53852614-53852664	SK-N-SH	brain:	n/a
12	chr15:53841455-53841505	HMEC	breast:	n/a
13	chr15:53852614-53852664	Hela-S3	cervix:	n/a
14	chr15:53852614-53852664	HUVEC	blood vessel:	n/a
15	chr15:53852614-53852664	IMR90	lung:	fetal
16	chr15:53852614-53852664	HCT-116	colon:	n/a
17	chr15:53841455-53841505	Hepatocyte	liver:	n/a
18	chr15:53841455-53841505	AG04450	lung:	fetal
19	chr15:53841455-53841505	H1-hESC	embryonic stem cell:	embryo
20	chr15:53841455-53841505	Jurkat	blood:	n/a
21	chr15:53841455-53841505	LNCaP	prostate:	n/a
22	chr15:53841455-53841505	BJ	skin:	n/a
23	chr15:53841455-53841505	PFSK-1	brain:	n/a
24	chr15:53852614-53852664	H1-hESC	embryonic stem cell:	embryo
25	chr15:53852614-53852664	AG09319	gingival:	n/a
26	chr15:53852614-53852664	AG04449	skin:	fetal
27	chr15:53841455-53841505	Hela-S3	cervix:	n/a
28	chr15:53841455-53841505	U87	brain:	n/a
29	chr15:53841455-53841505	BE2_C	brain:	n/a
30	chr15:53841455-53841505	GM12891	blood:	n/a
31	chr15:53841455-53841505	HCM	heart:	n/a
32	chr15:53841455-53841505	ECC-1	luminal epithelium:	n/a
33	chr15:53841455-53841505	HL-60	blood:	n/a
34	chr15:53852614-53852664	HCPEpiC	choroid plexus:	n/a
35	chr15:53841455-53841505	HepG2	liver:	n/a
36	chr15:53841455-53841505	SK-N-SH	brain:	n/a
37	chr15:53841455-53841505	HAEpiC	amniotic membrane:	n/a
38	chr15:53852614-53852664	HRE	kidney:	n/a
39	chr15:53852614-53852664	NHBE	bronchial:	n/a
40	chr15:53852614-53852664	HMEC	breast:	n/a
41	chr15:53841455-53841505	NT2-D1	testis:	n/a
42	chr15:53852614-53852664	SAEC	small airway:	n/a
43	chr15:53852614-53852664	LNCaP	prostate:	n/a
44	chr15:53841455-53841505	K562	blood:	n/a
45	chr15:53852614-53852664	Caco-2	colon:	n/a
46	chr15:53841455-53841505	AG10803	skin:	n/a
47	chr15:53852614-53852664	HepG2	liver:	n/a
48	chr15:53852614-53852664	AoSMC	blood vessel:	n/a
49	chr15:53852614-53852664	HEEpiC	esophagus:	n/a
50	chr15:53841455-53841505	AG04449	skin:	fetal

(count:14 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:53839749..53842575-chr15:53848742..53851441,2	MCF-7	breast:
2	chr15:53854915..53857646-chr15:53874393..53876986,2	MCF-7	breast:
3	chr15:53859427..53861280-chr15:53864189..53866503,2	MCF-7	breast:
4	chr15:53839734..53842688-chr15:53844777..53846540,2	K562	blood:
5	chr15:53847180..53849439-chr15:53853767..53855337,2	MCF-7	breast:
6	chr15:53847180..53849439-chr15:53853767..53855337,2	MCF-7	breast:
7	chr15:53827679..53829939-chr15:53831104..53833276,2	MCF-7	breast:
8	chr15:53839488..53841156-chr15:53845536..53848480,2	MCF-7	breast:
9	chr15:53839749..53842575-chr15:53848742..53851441,2	MCF-7	breast:
10	chr15:53839488..53841156-chr15:53845536..53848480,2	MCF-7	breast:
11	chr15:53824780..53826743-chr15:53827628..53831569,3	MCF-7	breast:
12	chr15:53852608..53853531-chr3:63859887..63860601,2	MCF-7	breast:
13	chr15:53827679..53829939-chr15:53831104..53833276,2	MCF-7	breast:
14	chr15:53839734..53842688-chr15:53844777..53846540,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-WDR72-2	chr15:53833087-53833300	NONHSAT043967
2	lnc-WDR72-2	chr15:53832859-53833049	NONHSAT043966

No data

Variant related genes	Relation type
WDR72	TF binding region
WDR72	CpG island

Extended variants
information (count: 1220 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:1220 , 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	rs12907854	chr15:53828686-53828687	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs573309450	chr15:53828695-53828696	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs547122462	chr15:53828728-53828729	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs145428239	chr15:53828797-53828798	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs16966177	chr15:53828832-53828833	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
6	rs148786099	chr15:53828841-53828842	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs17729707	chr15:53828859-53828860	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs527438437	chr15:53828917-53828918	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs547725774	chr15:53828970-53828971	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs375421299	chr15:53829029-53829030	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs113886693	chr15:53829030-53829031	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs191170666	chr15:53829034-53829035	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs183648752	chr15:53829061-53829062	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs570087427	chr15:53829075-53829076	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs371363706	chr15:53829076-53829077	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs372466340	chr15:53829113-53829114	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs142404827	chr15:53829157-53829158	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs375766641	chr15:53829163-53829164	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs577072618	chr15:53829174-53829175	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs4468550	chr15:53829195-53829196	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs568264311	chr15:53829224-53829225	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs373304089	chr15:53829247-53829248	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs74017422	chr15:53829285-53829286	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs190197516	chr15:53829304-53829305	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs538111019	chr15:53829314-53829315	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs79407673	chr15:53829338-53829339	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs182383320	chr15:53829391-53829392	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs535869451	chr15:53829396-53829397	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs556107752	chr15:53829403-53829404	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs534021650	chr15:53829453-53829454	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs187379392	chr15:53829457-53829458	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs7178004	chr15:53829513-53829514	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs570267656	chr15:53829534-53829535	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs564789047	chr15:53829589-53829590	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs572152741	chr15:53829610-53829611	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs572312973	chr15:53829647-53829648	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs190174178	chr15:53829695-53829696	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs541227068	chr15:53829737-53829738	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs370984903	chr15:53829748-53829749	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs561195532	chr15:53829773-53829774	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs530000613	chr15:53829786-53829787	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs543319198	chr15:53829803-53829804	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs181682779	chr15:53829839-53829840	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs185580708	chr15:53829896-53829897	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs552648438	chr15:53829903-53829904	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs578235678	chr15:53830056-53830057	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs545603267	chr15:53830062-53830063	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs151292987	chr15:53830082-53830083	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs528707041	chr15:53830097-53830098	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs554336194	chr15:53830119-53830120	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:57)

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
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

Chromatin state (count:177 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:53817400-53839400	Weak transcription	Liver	Liver
2	chr15:53823200-53832000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
3	chr15:53827600-53829400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr15:53827800-53829200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
5	chr15:53828000-53829000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
6	chr15:53828200-53829600	Enhancers	Brain Germinal Matrix	brain
7	chr15:53828400-53828800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr15:53828600-53829200	Flanking Active TSS	A549	lung
9	chr15:53828600-53829400	Enhancers	HepG2	liver
10	chr15:53828600-53829800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr15:53828800-53829000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr15:53828800-53829200	Enhancers	NH-A	brain
13	chr15:53829000-53829400	Enhancers	Cortex derived primary cultured neurospheres	brain
14	chr15:53829000-53832400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr15:53829200-53829800	Enhancers	A549	lung
16	chr15:53829800-53831400	Weak transcription	A549	lung
17	chr15:53831400-53831600	Enhancers	HUES6 Cell Line	embryonic stem cell
18	chr15:53831400-53832600	Enhancers	A549	lung
19	chr15:53831600-53832000	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
20	chr15:53831600-53832200	Active TSS	iPS-15b Cell Line	embryonic stem cell
21	chr15:53832000-53832800	Active TSS	ES-WA7 Cell Line	embryonic stem cell
22	chr15:53832000-53833000	Active TSS	HUES64 Cell Line	embryonic stem cell
23	chr15:53832000-53833400	Active TSS	ES-I3 Cell Line	embryonic stem cell
24	chr15:53832000-53833400	Active TSS	HUES6 Cell Line	embryonic stem cell
25	chr15:53832200-53832600	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
26	chr15:53832200-53833000	Active TSS	HUES48 Cell Line	embryonic stem cell
27	chr15:53832200-53833200	Active TSS	H1 Cell Line	embryonic stem cell
28	chr15:53832400-53832800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr15:53832400-53833000	Active TSS	iPS-18 Cell Line	embryonic stem cell
30	chr15:53832400-53833400	Active TSS	H9 Cell Line	embryonic stem cell
31	chr15:53832600-53833200	Active TSS	iPS-15b Cell Line	embryonic stem cell
32	chr15:53832800-53833200	Active TSS	Placenta	Placenta
33	chr15:53833200-53833600	Weak transcription	H1 Cell Line	embryonic stem cell
34	chr15:53833600-53833800	Enhancers	H1 Cell Line	embryonic stem cell
35	chr15:53839400-53840800	Strong transcription	Liver	Liver
36	chr15:53840200-53842400	Enhancers	HepG2	liver
37	chr15:53840400-53841000	Enhancers	Cortex derived primary cultured neurospheres	brain
38	chr15:53840400-53842400	Enhancers	iPS-18 Cell Line	embryonic stem cell
39	chr15:53840800-53842000	Weak transcription	Liver	Liver
40	chr15:53840800-53842600	Enhancers	HUES64 Cell Line	embryonic stem cell
41	chr15:53841000-53842400	Enhancers	HUES6 Cell Line	embryonic stem cell
42	chr15:53841000-53842600	Enhancers	HUES48 Cell Line	embryonic stem cell
43	chr15:53841000-53842600	Enhancers	iPS-15b Cell Line	embryonic stem cell
44	chr15:53841200-53842000	Enhancers	ES-I3 Cell Line	embryonic stem cell
45	chr15:53841200-53842200	Enhancers	H1 Cell Line	embryonic stem cell
46	chr15:53841400-53841600	Enhancers	Sigmoid Colon	Sigmoid Colon
47	chr15:53841400-53842400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
48	chr15:53841600-53841800	Enhancers	Duodenum Mucosa	Duodenum
49	chr15:53841800-53842200	Flanking Active TSS	Duodenum Mucosa	Duodenum
50	chr15:53841800-53842600	Enhancers	Fetal Intestine Small	intestine

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