Variant report

Variant	nsv1048248
Chromosome Location	chr15:34931178-34985414
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:569)
CpG islands
(count:0)
Chromatin interactive
region (count:50)
LncRNA
region (count:12)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:569 , 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	chr15:34954510-34955719	K562	blood:	n/a	n/a
2	ARID3A	chr15:34948740-34948973	K562	blood:	n/a	n/a
3	ARID3A	chr15:34946314-34948129	K562	blood:	n/a	n/a
4	ARID3A	chr15:34952157-34952158	K562	blood:	n/a	n/a
5	ARID3A	chr15:34944080-34945342	K562	blood:	n/a	n/a
6	ARID3A	chr15:34949658-34950365	K562	blood:	n/a	n/a
7	ARID3A	chr15:34953056-34953951	K562	blood:	n/a	n/a
8	ARID3A	chr15:34939172-34940883	K562	blood:	n/a	n/a
9	ATF1	chr15:34940100-34940799	K562	blood:	n/a	n/a
10	ATF1	chr15:34936394-34936711	K562	blood:	n/a	n/a
11	ATF1	chr15:34944877-34945255	K562	blood:	n/a	n/a
12	ATF1	chr15:34946741-34947211	K562	blood:	n/a	n/a
13	ATF1	chr15:34949656-34950320	K562	blood:	n/a	n/a
14	ATF1	chr15:34947575-34947975	K562	blood:	n/a	n/a
15	ATF2	chr15:34942304-34942739	GM12878	blood:	n/a	n/a
16	ATF2	chr15:34942319-34942566	GM12878	blood:	n/a	n/a
17	BACH1	chr15:34949732-34950003	K562	blood:	n/a	n/a
18	BACH1	chr15:34944497-34944500	K562	blood:	n/a	n/a
19	BATF	chr15:34942288-34942693	GM12878	blood:	n/a	chr15:34942439-34942449 chr15:34942438-34942449
20	BATF	chr15:34942205-34942724	GM12878	blood:	n/a	chr15:34942439-34942449 chr15:34942438-34942449
21	BCL11A	chr15:34942342-34942649	GM12878	blood:	n/a	n/a
22	BCL11A	chr15:34942273-34942696	GM12878	blood:	n/a	n/a
23	BCLAF1	chr15:34949675-34950412	K562	blood:	n/a	n/a
24	BCLAF1	chr15:34946604-34947084	K562	blood:	n/a	chr15:34946703-34946712
25	BHLHE40	chr15:34949672-34950063	K562	blood:	n/a	n/a
26	BHLHE40	chr15:34957939-34958132	K562	blood:	n/a	n/a
27	BHLHE40	chr15:34952400-34952527	K562	blood:	n/a	n/a
28	BHLHE40	chr15:34944964-34945198	K562	blood:	n/a	n/a
29	BHLHE40	chr15:34947721-34947910	K562	blood:	n/a	n/a
30	BHLHE40	chr15:34942322-34942647	K562	blood:	n/a	n/a
31	BRCA1	chr15:34971598-34971907	Hela-S3	cervix:	n/a	n/a
32	CBX3	chr15:34983145-34983500	K562	blood:	n/a	n/a
33	CBX3	chr15:34936200-34936568	K562	blood:	n/a	n/a
34	CBX3	chr15:34936154-34936713	K562	blood:	n/a	n/a
35	CBX3	chr15:34982373-34982645	K562	blood:	n/a	n/a
36	CCNT2	chr15:34946815-34947164	K562	blood:	n/a	n/a
37	CCNT2	chr15:34949582-34950219	K562	blood:	n/a	n/a
38	CCNT2	chr15:34947583-34947948	K562	blood:	n/a	n/a
39	CCNT2	chr15:34944905-34945202	K562	blood:	n/a	chr15:34945126-34945135
40	CEBPB	chr15:34944749-34945151	K562	blood:	n/a	chr15:34944767-34944778
41	CEBPB	chr15:34974878-34975174	Hela-S3	cervix:	n/a	n/a
42	CEBPB	chr15:34936361-34936644	K562	blood:	n/a	n/a
43	CEBPB	chr15:34940084-34940856	K562	blood:	n/a	n/a
44	CEBPB	chr15:34978737-34978961	Hela-S3	cervix:	n/a	n/a
45	CEBPB	chr15:34971468-34971933	Hela-S3	cervix:	n/a	n/a
46	CEBPB	chr15:34946648-34947780	K562	blood:	n/a	chr15:34947367-34947378 chr15:34947367-34947380
47	CEBPB	chr15:34949909-34950147	K562	blood:	n/a	n/a
48	CEBPB	chr15:34942355-34942966	IMR90	lung:	n/a	n/a
49	CEBPB	chr15:34936245-34936728	IMR90	lung:	n/a	n/a
50	CEBPB	chr15:34936375-34936702	Hela-S3	cervix:	n/a	n/a

No data

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

No.	Distal block	Cell Line	Cell type
1	chr15:34962423..34964134-chr15:34966956..34969710,3	K562	blood:
2	chr15:34960754..34962321-chr15:34966390..34968165,2	K562	blood:
3	chr15:34953069..34954628-chr15:34955083..34957176,2	K562	blood:
4	chr15:34965205..34967093-chr15:34977923..34979811,2	K562	blood:
5	chr15:34946410..34947955-chr15:34948303..34950980,2	K562	blood:
6	chr15:34965188..34969119-chr15:34970987..34974956,6	K562	blood:
7	chr15:34937548..34939695-chr15:34950801..34953012,2	K562	blood:
8	chr15:34907702..34910411-chr15:34952455..34954523,2	K562	blood:
9	chr15:34941429..34944034-chr15:34952465..34954233,2	K562	blood:
10	chr15:34980841..34982732-chr15:34984201..34987180,2	K562	blood:
11	chr15:34965205..34967093-chr15:34977923..34979811,2	K562	blood:
12	chr15:34931128..34933994-chr15:34934903..34936649,2	K562	blood:
13	chr15:34934770..34937620-chr15:34950647..34953239,2	K562	blood:
14	chr15:34933035..34934548-chr15:34938251..34939915,2	K562	blood:
15	chr15:34958499..34960200-chr15:34963239..34965401,2	K562	blood:
16	chr15:34934825..34936603-chr15:34945044..34948146,4	K562	blood:
17	chr15:34962423..34964134-chr15:34966956..34969710,3	K562	blood:
18	chr15:34937548..34939695-chr15:34950801..34953012,2	K562	blood:
19	chr15:34960285..34962774-chr15:34963252..34966258,4	K562	blood:
20	chr15:34983713..34985317-chr6:26197593..26200143,2	K562	blood:
21	chr15:34941344..34943269-chr15:34977002..34979213,2	K562	blood:
22	chr15:34934770..34937620-chr15:34950647..34953239,2	K562	blood:
23	chr15:34941344..34943269-chr15:34977002..34979213,2	K562	blood:
24	chr15:34963103..34965254-chr15:34966851..34969218,2	MCF-7	breast:
25	chr15:34941429..34944034-chr15:34952465..34954233,2	K562	blood:
26	chr15:34962434..34964585-chr15:34966364..34969710,3	K562	blood:
27	chr15:34962434..34964585-chr15:34966364..34969710,3	K562	blood:
28	chr15:34958499..34960200-chr15:34963239..34965401,2	K562	blood:
29	chr15:34960754..34962321-chr15:34966390..34968165,2	K562	blood:
30	chr15:34965468..34967744-chr15:34968524..34970610,2	K562	blood:
31	chr15:34940257..34942550-chr15:34950335..34951889,2	K562	blood:
32	chr15:34940940..34942564-chr15:34999108..35001019,2	K562	blood:
33	chr15:34931128..34933994-chr15:34934903..34936649,2	K562	blood:
34	chr15:34949750..34952665-chr15:35241317..35244101,2	K562	blood:
35	chr15:34946410..34947955-chr15:34948303..34950980,2	K562	blood:
36	chr15:34963103..34965254-chr15:34966851..34969218,2	MCF-7	breast:
37	chr15:34927785..34933151-chr15:34934497..34941490,8	K562	blood:
38	chr15:34960285..34962774-chr15:34963252..34966258,4	K562	blood:
39	chr15:34927785..34933151-chr15:34934497..34941490,8	K562	blood:
40	chr15:34965188..34969119-chr15:34970987..34974956,6	K562	blood:
41	chr15:34949722..34952645-chr15:34986997..34989606,2	K562	blood:
42	chr15:34940257..34942550-chr15:34950335..34951889,2	K562	blood:
43	chr15:34953489..34955951-chr15:35181219..35183157,2	K562	blood:
44	chr15:34933035..34934548-chr15:34938251..34939915,2	K562	blood:
45	chr15:34980841..34982732-chr15:34984201..34987180,2	K562	blood:
46	chr15:34913307..34914991-chr15:34929235..34931577,2	K562	blood:
47	chr15:34953069..34954628-chr15:34955083..34957176,2	K562	blood:
48	chr15:34983650..34987842-chr15:34989482..34992979,5	K562	blood:
49	chr15:34965468..34967744-chr15:34968524..34970610,2	K562	blood:
50	chr15:34983650..34987345-chr15:34990001..34992979,4	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GOLGA8A-1	chr15:34947820-34947978	XLOC_011421
2	lnc-GOLGA8A-1	chr15:34962302-34962370	XLOC_011421
3	lnc-GOLGA8A-1	chr15:34946499-34946618	ENSG00000261304.1
4	lnc-GOLGA8A-1	chr15:34943885-34943977	ENSG00000261304.1
5	lnc-GOLGA8A-1	chr15:34943336-34943463	ENSG00000261304.1
6	lnc-GOLGA8A-1	chr15:34948237-34948332	ucscGeneNc_uc001zji_1
7	lnc-AC114546.1-13	chr15:34972962-34973170	uc_385_+
8	lnc-GJD2-2	chr15:34972962-34973170	uc_385_-
9	lnc-GOLGA8A-1	chr15:34947820-34947965	ENSG00000261304.1
10	lnc-GOLGA8A-1	chr15:34943936-34946139	ucscGeneNc_uc001zji_1
11	lnc-GJD2-1	chr15:34967556-34967834	XLOC_011422
12	lnc-AC114546.1-12	chr15:34982173-34982277	NONHSAT041602

No data

Variant related genes	Relation type
ENSG00000261304	TF binding region
ENSG00000197409	chromatin interactions
ENSG00000196866	chromatin interactions
ENSG00000261304	chromatin interactions
ENSG00000197846	chromatin interactions
NEK9	miRNA target sites
NEK7	miRNA target sites

Extended variants
information (count: 1967 )
Associated
traits (count: 69 )

Variant overlapped rSNPs/rCNVs (count:1967 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11632459	chr15:34931178-34931179	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs143465011	chr15:34931208-34931209	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs192012268	chr15:34931226-34931227	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs561745384	chr15:34931240-34931241	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs529390358	chr15:34931274-34931275	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs541476722	chr15:34931286-34931287	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs8027939	chr15:34931364-34931365	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
8	rs527450171	chr15:34931421-34931422	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs8032169	chr15:34931431-34931432	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs570755838	chr15:34931476-34931477	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs184857901	chr15:34931499-34931500	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs549847323	chr15:34931505-34931506	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs568053935	chr15:34931544-34931545	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs10519944	chr15:34931572-34931573	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs147134229	chr15:34931598-34931599	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs189658429	chr15:34931625-34931626	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs368659034	chr15:34931626-34931627	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs540060157	chr15:34931707-34931708	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs180883940	chr15:34931745-34931746	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs186246442	chr15:34931748-34931749	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs552952439	chr15:34931766-34931767	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs35426950	chr15:34931768-34931769	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs138966201	chr15:34931818-34931819	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs149434912	chr15:34931831-34931832	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs115870557	chr15:34931859-34931860	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs144814972	chr15:34931870-34931871	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs188139820	chr15:34931919-34931920	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs578020667	chr15:34931951-34931952	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs148562445	chr15:34932081-34932082	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs564268295	chr15:34932083-34932084	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs181968312	chr15:34932122-34932123	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs6495698	chr15:34932123-34932124	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs561670574	chr15:34932124-34932125	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs1836973	chr15:34932230-34932231	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs547063537	chr15:34932303-34932304	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs565796616	chr15:34932308-34932309	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs539157323	chr15:34932343-34932344	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs12915365	chr15:34932356-34932357	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs143627638	chr15:34932359-34932360	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs576031543	chr15:34932388-34932389	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs7403222	chr15:34932389-34932390	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs186190897	chr15:34932390-34932391	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs573710505	chr15:34932398-34932399	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs7403224	chr15:34932405-34932406	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs146792813	chr15:34932430-34932431	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs578082738	chr15:34932476-34932477	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs545161826	chr15:34932492-34932493	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs564282430	chr15:34932559-34932560	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs201727520	chr15:34932573-34932574	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs576742504	chr15:34932646-34932647	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:69)

Disease	PMID	Source
HDAC8	0	CNVD
NIPBL	0	CNVD
RAD21	0	CNVD
SMC1A	0	CNVD
SMC3	0	CNVD
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Angelman syndrome	16183798	CNVD
Acute lymphoblastic leukemia	20067559	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
Hodgkin''s lymphoma	18641027	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
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Breast cancer	17133270	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
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21785460	CNVD
Abnormal corpus callosum	21572526	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Autism	19204725	CNVD
Schizophrenia	19204725	CNVD
Schizophrenia	19149910	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Legius syndrome	19443465	CNVD
Holoprosencephaly	21359414	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Prader-willi syndrome	21504564	CNVD
Cancer	17440070	CNVD
Basal cell lymphoma	17053054	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
lymphocytic leukemia	21291569	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:179 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:34929400-34931400	Weak transcription	K562	blood
2	chr15:34931400-34932800	Enhancers	K562	blood
3	chr15:34932600-34932800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
4	chr15:34932800-34934400	Weak transcription	K562	blood
5	chr15:34932800-34936200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
6	chr15:34934400-34934600	Active TSS	ES-I3 Cell Line	embryonic stem cell
7	chr15:34934400-34935200	Enhancers	K562	blood
8	chr15:34934600-34934800	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
9	chr15:34935200-34935800	Weak transcription	K562	blood
10	chr15:34935800-34937400	ZNF genes & repeats	K562	blood
11	chr15:34936000-34936200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
12	chr15:34936000-34937000	Enhancers	HSMM	muscle
13	chr15:34936200-34936600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
14	chr15:34936200-34936600	Enhancers	HUVEC	blood vessel
15	chr15:34936200-34937200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr15:34936200-34937200	Enhancers	Muscle Satellite Cultured Cells	--
17	chr15:34936200-34942200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
18	chr15:34936400-34936600	Enhancers	NHLF	lung
19	chr15:34936400-34936800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr15:34936600-34936800	Enhancers	HUES64 Cell Line	embryonic stem cell
21	chr15:34936600-34936800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
22	chr15:34936600-34937200	Enhancers	NH-A	brain
23	chr15:34936600-34937600	Enhancers	HSMMtube	muscle
24	chr15:34936600-34942200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
25	chr15:34936600-34944200	Weak transcription	HUVEC	blood vessel
26	chr15:34936800-34940600	Weak transcription	HUES64 Cell Line	embryonic stem cell
27	chr15:34937000-34942200	Weak transcription	HSMM	muscle
28	chr15:34937200-34941400	Weak transcription	Muscle Satellite Cultured Cells	--
29	chr15:34937200-34942000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr15:34937200-34942200	Weak transcription	NH-A	brain
31	chr15:34937400-34938000	Weak transcription	K562	blood
32	chr15:34937600-34941800	Weak transcription	HSMMtube	muscle
33	chr15:34938000-34938800	Flanking Active TSS	K562	blood
34	chr15:34938800-34939000	Enhancers	HUES48 Cell Line	embryonic stem cell
35	chr15:34938800-34939200	Active TSS	K562	blood
36	chr15:34939200-34940400	Weak transcription	HUES48 Cell Line	embryonic stem cell
37	chr15:34939200-34941000	Flanking Active TSS	K562	blood
38	chr15:34940200-34940400	Enhancers	Aorta	Aorta
39	chr15:34940400-34941000	Enhancers	HUES48 Cell Line	embryonic stem cell
40	chr15:34940400-34941000	Enhancers	iPS-15b Cell Line	embryonic stem cell
41	chr15:34940400-34941200	Enhancers	ES-I3 Cell Line	embryonic stem cell
42	chr15:34940600-34941000	Enhancers	HUES64 Cell Line	embryonic stem cell
43	chr15:34941000-34944600	Enhancers	K562	blood
44	chr15:34941200-34941400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
45	chr15:34941200-34949200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
46	chr15:34941400-34942200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
47	chr15:34941400-34942800	Enhancers	Muscle Satellite Cultured Cells	--
48	chr15:34941800-34943400	Enhancers	HSMMtube	muscle
49	chr15:34942000-34943000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
50	chr15:34942200-34942600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung

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