Variant report

Variant	nsv428637
Chromosome Location	chr15:54279125-54500755
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:521)
CpG islands
(count:244)
Chromatin interactive
region (count:26)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:521 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr15:54442511-54442890	GM12878	blood:	n/a	n/a
2	BATF	chr15:54442487-54442777	GM12878	blood:	n/a	n/a
3	BATF	chr15:54406133-54406329	GM12878	blood:	n/a	n/a
4	BCL11A	chr15:54442401-54442874	GM12878	blood:	n/a	n/a
5	BCL11A	chr15:54442387-54442927	GM12878	blood:	n/a	n/a
6	BCL3	chr15:54375816-54376051	GM12878	blood:	n/a	n/a
7	BCLAF1	chr15:54442495-54442836	GM12878	blood:	n/a	n/a
8	BHLHE40	chr15:54358727-54358963	GM12878	blood:	n/a	n/a
9	BHLHE40	chr15:54375171-54375297	GM12878	blood:	n/a	n/a
10	BHLHE40	chr15:54442366-54442968	GM12878	blood:	n/a	n/a
11	BRCA1	chr15:54375208-54375398	GM12878	blood:	n/a	n/a
12	BRCA1	chr15:54376140-54376218	GM12878	blood:	n/a	n/a
13	CEBPB	chr15:54327914-54328190	A549	lung:	n/a	chr15:54328041-54328052
14	CEBPB	chr15:54317233-54317453	IMR90	lung:	n/a	n/a
15	CEBPB	chr15:54334058-54334298	IMR90	lung:	n/a	n/a
16	CEBPB	chr15:54327869-54328210	HepG2	liver:	n/a	chr15:54328041-54328052
17	CEBPB	chr15:54335334-54335567	HepG2	liver:	n/a	chr15:54335407-54335420 chr15:54335407-54335420
18	CEBPB	chr15:54442428-54442789	IMR90	lung:	n/a	n/a
19	CEBPB	chr15:54327868-54328211	Hela-S3	cervix:	n/a	chr15:54328041-54328052
20	CEBPB	chr15:54411288-54411565	HepG2	liver:	n/a	n/a
21	CEBPB	chr15:54338360-54338559	A549	lung:	n/a	n/a
22	CEBPB	chr15:54405089-54405315	HepG2	liver:	n/a	n/a
23	CHD1	chr15:54375292-54375397	GM12878	blood:	n/a	n/a
24	CHD2	chr15:54395054-54395191	GM12878	blood:	n/a	n/a
25	CHD2	chr15:54375592-54375770	GM12878	blood:	n/a	n/a
26	CHD2	chr15:54375231-54375384	GM12878	blood:	n/a	n/a
27	CHD2	chr15:54383047-54383312	GM12878	blood:	n/a	chr15:54383265-54383275
28	CHD2	chr15:54380837-54380897	GM12878	blood:	n/a	n/a
29	CHD2	chr15:54442444-54442924	GM12878	blood:	n/a	n/a
30	CHD2	chr15:54434965-54434973	GM12878	blood:	n/a	n/a
31	CTCF	chr15:54375127-54375366	K562	blood:	n/a	n/a
32	CTCF	chr15:54375180-54375330	GM12873	blood:	n/a	n/a
33	CTCF	chr15:54375160-54375310	K562	blood:	n/a	n/a
34	CTCF	chr15:54375160-54375310	AG04450	lung:	n/a	n/a
35	CTCF	chr15:54374860-54375010	HCT-116	colon:	n/a	n/a
36	CTCF	chr15:54375220-54375370	HA-sp	spinal cord:	n/a	n/a
37	CTCF	chr15:54374967-54375523	MCF-7	breast:	n/a	n/a
38	CTCF	chr15:54375160-54375310	HCPEpiC	choroid plexus:	n/a	n/a
39	CTCF	chr15:54375180-54375330	HPF	lung:	n/a	n/a
40	CTCF	chr15:54375059-54375444	IMR90	lung:	n/a	n/a
41	CTCF	chr15:54375200-54375350	HUVEC	blood vessel:	n/a	n/a
42	CTCF	chr15:54375100-54375250	BJ	skin:	n/a	n/a
43	CTCF	chr15:54358550-54358924	GM12878	blood:	n/a	n/a
44	CTCF	chr15:54375084-54375394	GM19239	blood:	n/a	n/a
45	CTCF	chr15:54419474-54419512	Kidney_OC	kidney:	n/a	n/a
46	CTCF	chr15:54472238-54472296	GM13976	blood:	n/a	n/a
47	CTCF	chr15:54375200-54375350	MCF-7	breast:	n/a	n/a
48	CTCF	chr15:54375140-54375339	Hela-S3	cervix:	n/a	n/a
49	CTCF	chr15:54374988-54375622	A549	lung:	n/a	n/a
50	CTCF	chr15:54375200-54375350	HBMEC	blood vessel:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:54305206-54305256	BJ	skin:	n/a
2	chr15:54303927-54303977	NT2-D1	testis:	n/a
3	chr15:54303927-54303977	MCF10A-Er-Src	breast:	n/a
4	chr15:54305206-54305256	HRCEpiC	kidney:	n/a
5	chr15:54303927-54303977	K562	blood:	n/a
6	chr15:54304778-54304828	LNCaP	prostate:	n/a
7	chr15:54305206-54305256	Hela-S3	cervix:	n/a
8	chr15:54304778-54304828	U87	brain:	n/a
9	chr15:54304950-54305000	T-47D	breast:	n/a
10	chr15:54303927-54303977	MCF-7	breast:	n/a
11	chr15:54304778-54304828	ovcar-3	ovarian:	n/a
12	chr15:54304778-54304828	AG09319	gingival:	n/a
13	chr15:54304778-54304828	T-47D	breast:	n/a
14	chr15:54303927-54303977	SK-N-MC	brain:	n/a
15	chr15:54304950-54305000	HCT-116	colon:	n/a
16	chr15:54305206-54305256	AoSMC	blood vessel:	n/a
17	chr15:54305206-54305256	HEEpiC	esophagus:	n/a
18	chr15:54303927-54303977	H1-hESC	embryonic stem cell:	embryo
19	chr15:54304950-54305000	RPTEC	kidney:	n/a
20	chr15:54304778-54304828	SKMC	muscle:	n/a
21	chr15:54304778-54304828	SK-N-MC	brain:	n/a
22	chr15:54304950-54305000	ECC-1	luminal epithelium:	n/a
23	chr15:54305206-54305256	MCF-7	breast:	n/a
24	chr15:54303927-54303977	HUVEC	blood vessel:	n/a
25	chr15:54303927-54303977	SKMC	muscle:	n/a
26	chr15:54305206-54305256	GM12878	blood:	n/a
27	chr15:54303927-54303977	NH-A	brain:	n/a
28	chr15:54304778-54304828	HMEC	breast:	n/a
29	chr15:54305206-54305256	ovcar-3	ovarian:	n/a
30	chr15:54304778-54304828	PANC-1	pancreas:	n/a
31	chr15:54304950-54305000	SAEC	small airway:	n/a
32	chr15:54304778-54304828	ECC-1	luminal epithelium:	n/a
33	chr15:54304950-54305000	SK-N-MC	brain:	n/a
34	chr15:54305206-54305256	K562	blood:	n/a
35	chr15:54304778-54304828	HCT-116	colon:	n/a
36	chr15:54305206-54305256	RPTEC	kidney:	n/a
37	chr15:54304778-54304828	HUVEC	blood vessel:	n/a
38	chr15:54305206-54305256	AG04449	skin:	fetal
39	chr15:54305206-54305256	GM19239	blood:	n/a
40	chr15:54305206-54305256	HNPCEpiC	eye:	n/a
41	chr15:54305206-54305256	U87	brain:	n/a
42	chr15:54303927-54303977	NB4	blood:	n/a
43	chr15:54303927-54303977	GM19239	blood:	n/a
44	chr15:54304778-54304828	PFSK-1	brain:	n/a
45	chr15:54304778-54304828	HCF	heart:	n/a
46	chr15:54304778-54304828	Caco-2	colon:	n/a
47	chr15:54305206-54305256	HEK293	kidney:	embryo
48	chr15:54305206-54305256	SKMC	muscle:	n/a
49	chr15:54304778-54304828	K562	blood:	n/a
50	chr15:54304950-54305000	Hepatocyte	liver:	n/a

(count:26 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:54298660..54299394-chr15:54317743..54318508,2	MCF-7	breast:
2	chr15:54367693..54370404-chr15:54374986..54376971,2	MCF-7	breast:
3	chr15:54323697..54325296-chr15:54326702..54328336,2	MCF-7	breast:
4	chr15:54268767..54269686-chr15:54375127..54375711,4	MCF-7	breast:
5	chr15:54307497..54309750-chr15:54313366..54316109,2	K562	blood:
6	chr15:54316286..54318779-chr15:54320377..54322655,2	MCF-7	breast:
7	chr15:54428237..54428841-chr17:58520354..58521187,2	MCF-7	breast:
8	chr11:67937367..67938965-chr15:54485479..54488109,2	MCF-7	breast:
9	chr15:54323697..54325296-chr15:54326702..54328336,2	MCF-7	breast:
10	chr15:54468684..54471121-chr15:54610190..54612096,2	K562	blood:
11	chr15:54298660..54299394-chr15:54317743..54318508,2	MCF-7	breast:
12	chr15:54254977..54255831-chr15:54374717..54376166,5	MCF-7	breast:
13	chr15:54355045..54357590-chr15:54360185..54362187,2	K562	blood:
14	chr15:54307497..54309750-chr15:54313366..54316109,2	K562	blood:
15	chr15:54322544..54324113-chr15:54326394..54329349,2	K562	blood:
16	chr15:54272577..54275424-chr15:54278207..54281083,2	MCF-7	breast:
17	chr15:54316286..54318779-chr15:54320377..54322655,2	MCF-7	breast:
18	chr15:54374868..54376175-chr15:55400827..55401744,4	MCF-7	breast:
19	chr15:54467594..54469950-chr8:103818486..103820863,2	MCF-7	breast:
20	chr15:54375029..54375976-chr15:55400805..55401778,3	MCF-7	breast:
21	chr15:54438739..54441656-chr17:57920173..57923142,2	MCF-7	breast:
22	chr15:54367693..54370404-chr15:54374986..54376971,2	MCF-7	breast:
23	chr15:54254685..54255342-chr15:54375170..54375703,2	MCF-7	breast:
24	chr15:54355045..54357590-chr15:54360185..54362187,2	K562	blood:
25	chr15:54374784..54375687-chr15:55460665..55461171,2	MCF-7	breast:
26	chr15:54322544..54324113-chr15:54326394..54329349,2	K562	blood:

No data

Variant related genes	Relation type
UNC13C	TF binding region
ENSG00000259619	TF binding region
UNC13C	CpG island
ENSG00000259619	CpG island
ENSG00000259669	chromatin interactions
ENSG00000253669	chromatin interactions

Extended variants
information (count: 5369 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:5369 , 50 per page) page: 1 2 3 4 5 6 7 ... 108

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs142702107	chr15:54279131-54279132	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs563953961	chr15:54279149-54279150	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs386784102	chr15:54279157-54279158	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs56314416	chr15:54279158-54279159	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs559734873	chr15:54279171-54279172	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs56081015	chr15:54279178-54279179	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs547131064	chr15:54279188-54279189	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs544652490	chr15:54279216-54279217	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs367557055	chr15:54279229-54279230	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs529609010	chr15:54279241-54279242	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs2725592	chr15:54279249-54279250	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs569592375	chr15:54279291-54279292	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs538595444	chr15:54279332-54279333	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs558710468	chr15:54279360-54279361	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs17664323	chr15:54279372-54279373	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs115208329	chr15:54279385-54279386	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs554739247	chr15:54279402-54279403	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs143704085	chr15:54279452-54279453	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs368532118	chr15:54279457-54279458	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs372482714	chr15:54279488-54279489	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs59552006	chr15:54279494-54279495	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs377040841	chr15:54279544-54279545	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs17664329	chr15:54279570-54279571	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs557434658	chr15:54279574-54279575	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs560058288	chr15:54279580-54279581	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs577600935	chr15:54279587-54279588	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs546138573	chr15:54279693-54279694	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs145719556	chr15:54279729-54279730	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs527582526	chr15:54279731-54279732	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs533320470	chr15:54279738-54279739	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs574341960	chr15:54279749-54279750	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs386784103	chr15:54279758-54279759	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs11857334	chr15:54279759-54279760	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs373984607	chr15:54279770-54279771	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs78318987	chr15:54279822-54279823	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs542418386	chr15:54279837-54279838	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs181877206	chr15:54279842-54279843	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs529767445	chr15:54279845-54279846	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs139397123	chr15:54279862-54279863	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs74459932	chr15:54279868-54279869	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs569353503	chr15:54279869-54279870	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs59300979	chr15:54279871-54279872	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs373195756	chr15:54279904-54279905	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs552142547	chr15:54279917-54279918	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs186337630	chr15:54279918-54279919	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs991073	chr15:54279919-54279920	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs117126432	chr15:54279929-54279930	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs10518747	chr15:54279931-54279932	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs571230975	chr15:54279962-54279963	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs150886804	chr15:54279963-54279964	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:61)

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	21509527	CNVD
Urothelial carcinoma	21177765	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:169 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:54271800-54281200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr15:54277000-54283800	Weak transcription	Fetal Lung	lung
3	chr15:54278200-54283600	Weak transcription	Aorta	Aorta
4	chr15:54279800-54280200	Enhancers	iPS-18 Cell Line	embryonic stem cell
5	chr15:54280000-54280400	Enhancers	iPS-15b Cell Line	embryonic stem cell
6	chr15:54283800-54286000	ZNF genes & repeats	Fetal Lung	lung
7	chr15:54284400-54284600	ZNF genes & repeats	Aorta	Aorta
8	chr15:54285400-54285800	ZNF genes & repeats	Aorta	Aorta
9	chr15:54285800-54288200	Weak transcription	Aorta	Aorta
10	chr15:54286000-54302000	Weak transcription	Fetal Lung	lung
11	chr15:54288200-54288400	Enhancers	Aorta	Aorta
12	chr15:54288400-54288600	Weak transcription	Aorta	Aorta
13	chr15:54299600-54300200	ZNF genes & repeats	Aorta	Aorta
14	chr15:54300200-54305200	Weak transcription	Aorta	Aorta
15	chr15:54302000-54302800	Strong transcription	Fetal Lung	lung
16	chr15:54302800-54303200	Weak transcription	Fetal Lung	lung
17	chr15:54303200-54305400	Enhancers	Fetal Lung	lung
18	chr15:54303800-54304200	Enhancers	Cortex derived primary cultured neurospheres	brain
19	chr15:54304000-54310000	Weak transcription	Skeletal Muscle Female	skeletal muscle
20	chr15:54304600-54304800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
21	chr15:54305200-54305400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr15:54305200-54305400	Strong transcription	Aorta	Aorta
23	chr15:54305400-54306000	ZNF genes & repeats	Aorta	Aorta
24	chr15:54305400-54306600	Genic enhancers	Fetal Lung	lung
25	chr15:54305400-54310200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr15:54306000-54307000	Weak transcription	Aorta	Aorta
27	chr15:54306200-54306400	Enhancers	Skeletal Muscle Male	skeletal muscle
28	chr15:54306400-54310000	Weak transcription	Skeletal Muscle Male	skeletal muscle
29	chr15:54306600-54307400	Enhancers	Fetal Lung	lung
30	chr15:54307400-54308400	Weak transcription	Fetal Lung	lung
31	chr15:54308400-54308600	Enhancers	Fetal Lung	lung
32	chr15:54308600-54309000	Weak transcription	Fetal Lung	lung
33	chr15:54309000-54311000	Enhancers	Fetal Lung	lung
34	chr15:54309800-54311000	Enhancers	Colon Smooth Muscle	Colon
35	chr15:54309800-54311000	Enhancers	Fetal Brain Male	brain
36	chr15:54310000-54310400	Enhancers	Skeletal Muscle Female	skeletal muscle
37	chr15:54310000-54310400	Enhancers	Stomach Smooth Muscle	stomach
38	chr15:54310000-54311000	Enhancers	Skeletal Muscle Male	skeletal muscle
39	chr15:54310200-54310400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr15:54310200-54311000	Enhancers	Duodenum Smooth Muscle	Duodenum
41	chr15:54311000-54314000	Weak transcription	Fetal Brain Male	brain
42	chr15:54311000-54314000	Weak transcription	Fetal Lung	lung
43	chr15:54314000-54314600	ZNF genes & repeats	Fetal Lung	lung
44	chr15:54314600-54325200	Weak transcription	Fetal Lung	lung
45	chr15:54315600-54321800	Weak transcription	Aorta	Aorta
46	chr15:54319200-54319600	Enhancers	ES-I3 Cell Line	embryonic stem cell
47	chr15:54319600-54320200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
48	chr15:54319600-54322000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
49	chr15:54320200-54321800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
50	chr15:54321000-54322400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin

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