Variant report

Variant	nsv904100
Chromosome Location	chr15:40959624-40994706
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1161)
CpG islands
(count:1162)
Chromatin interactive
region (count:37)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1161 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:40986729-40987431	K562	blood:	n/a	chr15:40987362-40987370
2	ARID3A	chr15:40986800-40988040	HepG2	liver:	n/a	chr15:40987362-40987370
3	ARID3A	chr15:40987783-40988046	K562	blood:	n/a	n/a
4	ARID3A	chr15:40972423-40972739	HepG2	liver:	n/a	n/a
5	ATF1	chr15:40986771-40987514	K562	blood:	n/a	n/a
6	ATF2	chr15:40986858-40987587	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr15:40986312-40987561	GM12878	blood:	n/a	n/a
8	ATF2	chr15:40986495-40987421	GM12878	blood:	n/a	n/a
9	ATF2	chr15:40986938-40987557	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr15:40986805-40987346	H1-hESC	embryonic stem cell:	n/a	n/a
11	BCLAF1	chr15:40986513-40987617	GM12878	blood:	n/a	n/a
12	BCLAF1	chr15:40986314-40987827	GM12878	blood:	n/a	n/a
13	BCLAF1	chr15:40971237-40971625	GM12878	blood:	n/a	n/a
14	BHLHE40	chr15:40964809-40965074	GM12878	blood:	n/a	n/a
15	BHLHE40	chr15:40987072-40987320	A549	lung:	n/a	n/a
16	BHLHE40	chr15:40986451-40987790	GM12878	blood:	n/a	chr15:40987770-40987786 chr15:40987390-40987406
17	BHLHE40	chr15:40972359-40972610	HepG2	liver:	n/a	n/a
18	BHLHE40	chr15:40986587-40987915	K562	blood:	n/a	chr15:40987770-40987786 chr15:40987390-40987406
19	BHLHE40	chr15:40971308-40971607	GM12878	blood:	n/a	n/a
20	BRCA1	chr15:40986742-40987392	HepG2	liver:	n/a	n/a
21	BRCA1	chr15:40986656-40987442	GM12878	blood:	n/a	n/a
22	BRCA1	chr15:40971272-40971643	Hela-S3	cervix:	n/a	n/a
23	BRCA1	chr15:40986667-40987960	Hela-S3	cervix:	n/a	n/a
24	BRCA1	chr15:40986673-40987588	H1-hESC	embryonic stem cell:	n/a	n/a
25	CBX3	chr15:40971226-40971614	K562	blood:	n/a	n/a
26	CBX3	chr15:40986181-40988098	K562	blood:	n/a	n/a
27	CBX3	chr15:40986957-40987377	K562	blood:	n/a	n/a
28	CCNT2	chr15:40986783-40987845	K562	blood:	n/a	n/a
29	CEBPB	chr15:40986712-40988049	Hela-S3	cervix:	n/a	n/a
30	CEBPB	chr15:40986693-40987434	K562	blood:	n/a	n/a
31	CEBPB	chr15:40987049-40987475	IMR90	lung:	n/a	n/a
32	CEBPB	chr15:40984026-40984175	Hela-S3	cervix:	n/a	n/a
33	CEBPB	chr15:40987037-40987390	HepG2	liver:	n/a	n/a
34	CEBPB	chr15:40987113-40987325	HepG2	liver:	n/a	n/a
35	CEBPB	chr15:40972608-40972733	K562	blood:	n/a	n/a
36	CEBPB	chr15:40971298-40971678	K562	blood:	n/a	n/a
37	CEBPB	chr15:40986305-40987010	GM12878	blood:	n/a	n/a
38	CEBPB	chr15:40971327-40971705	K562	blood:	n/a	n/a
39	CEBPB	chr15:40971328-40971688	H1-hESC	embryonic stem cell:	n/a	n/a
40	CEBPB	chr15:40971316-40971688	HepG2	liver:	n/a	n/a
41	CEBPB	chr15:40971356-40971626	A549	lung:	n/a	n/a
42	CEBPB	chr15:40987041-40987394	A549	lung:	n/a	n/a
43	CEBPB	chr15:40972491-40972691	A549	lung:	n/a	n/a
44	CEBPB	chr15:40992597-40992774	K562	blood:	n/a	n/a
45	CEBPB	chr15:40992625-40992732	A549	lung:	n/a	n/a
46	CEBPB	chr15:40971371-40971594	ECC-1	luminal epithelium:	n/a	n/a
47	CEBPB	chr15:40986990-40987520	MCF-7	breast:	n/a	n/a
48	CEBPB	chr15:40971445-40971656	IMR90	lung:	n/a	n/a
49	CEBPB	chr15:40987032-40987383	K562	blood:	n/a	n/a
50	CEBPB	chr15:40971442-40971702	HepG2	liver:	n/a	n/a

(count:1162 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:40984679-40984729	HCPEpiC	choroid plexus:	n/a
2	chr15:40986962-40987012	AG10803	skin:	n/a
3	chr15:40986872-40986922	AG04450	lung:	fetal
4	chr15:40984679-40984729	HCPEpiC	choroid plexus:	n/a
5	chr15:40986962-40987012	AG10803	skin:	n/a
6	chr15:40986872-40986922	AG04450	lung:	fetal
7	chr15:40969417-40969467	HCF	heart:	n/a
8	chr15:40987790-40987840	GM12878	blood:	n/a
9	chr15:40987167-40987217	GM19239	blood:	n/a
10	chr15:40986923-40986973	HEEpiC	esophagus:	n/a
11	chr15:40987279-40987329	PFSK-1	brain:	n/a
12	chr15:40986702-40986752	HepG2	liver:	n/a
13	chr15:40987279-40987329	HCM	heart:	n/a
14	chr15:40987771-40987821	HL-60	blood:	n/a
15	chr15:40986872-40986922	Caco-2	colon:	n/a
16	chr15:40987673-40987723	CMK	blood:	n/a
17	chr15:40987279-40987329	Hepatocyte	liver:	n/a
18	chr15:40987167-40987217	BE2_C	brain:	n/a
19	chr15:40969222-40969272	ovcar-3	ovarian:	n/a
20	chr15:40990874-40990924	K562	blood:	n/a
21	chr15:40987107-40987157	HNPCEpiC	eye:	n/a
22	chr15:40987771-40987821	HPAEpiC	pulmonary alveolar:	n/a
23	chr15:40969222-40969272	SKMC	muscle:	n/a
24	chr15:40987107-40987157	PFSK-1	brain:	n/a
25	chr15:40969417-40969467	HUVEC	blood vessel:	n/a
26	chr15:40986962-40987012	BJ	skin:	n/a
27	chr15:40984679-40984729	BE2_C	brain:	n/a
28	chr15:40987279-40987329	HIPEpiC	eye:	n/a
29	chr15:40986962-40987012	T-47D	breast:	n/a
30	chr15:40986702-40986752	HL-60	blood:	n/a
31	chr15:40987107-40987157	U87	brain:	n/a
32	chr15:40987167-40987217	K562	blood:	n/a
33	chr15:40987009-40987059	HCPEpiC	choroid plexus:	n/a
34	chr15:40987209-40987259	SK-N-MC	brain:	n/a
35	chr15:40987107-40987157	MCF10A-Er-Src	breast:	n/a
36	chr15:40987404-40987454	SKMC	muscle:	n/a
37	chr15:40969417-40969467	AG04450	lung:	fetal
38	chr15:40987009-40987059	Caco-2	colon:	n/a
39	chr15:40987167-40987217	AG04449	skin:	fetal
40	chr15:40987279-40987329	HRCEpiC	kidney:	n/a
41	chr15:40987009-40987059	HIPEpiC	eye:	n/a
42	chr15:40987279-40987329	HMEC	breast:	n/a
43	chr15:40987368-40987418	AG04450	lung:	fetal
44	chr15:40986923-40986973	HRCEpiC	kidney:	n/a
45	chr15:40987009-40987059	SK-N-SH	brain:	n/a
46	chr15:40984679-40984729	GM12878	blood:	n/a
47	chr15:40969222-40969272	HCF	heart:	n/a
48	chr15:40986702-40986752	CMK	blood:	n/a
49	chr15:40987107-40987157	GM19239	blood:	n/a
50	chr15:40986702-40986752	HCPEpiC	choroid plexus:	n/a

(count:37 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:40986980..40987882-chr6:30584915..30585502,2	Hela-S3	cervix:
2	chr15:40986558..40989601-chr15:40990368..40993764,9	K562	blood:
3	chr15:40992580..40995462-chr15:41019256..41021826,2	K562	blood:
4	chr15:40980250..40982620-chr15:40989406..40991177,2	K562	blood:
5	chr15:40994380..40994911-chr15:41032177..41032692,2	MCF-7	breast:
6	chr15:40979214..40982658-chr15:40985781..40989168,4	MCF-7	breast:
7	chr15:40978878..40981252-chr15:41232643..41234691,2	MCF-7	breast:
8	chr15:40982126..40985382-chr15:40985435..40988081,4	MCF-7	breast:
9	chr15:40985736..40987452-chr15:41134754..41137017,2	MCF-7	breast:
10	chr15:40981084..40982802-chr15:40985711..40988453,2	K562	blood:
11	chr15:40987359..40990886-chr15:41044779..41048321,5	K562	blood:
12	chr15:40986884..40987798-chr15:41575787..41576375,2	Hela-S3	cervix:
13	chr15:40986691..40987408-chr2:71295417..71296023,2	Hela-S3	cervix:
14	chr15:40987298..40988058-chr17:62502299..62503222,2	Hela-S3	cervix:
15	chr15:40885583..40887494-chr15:40985320..40988301,2	K562	blood:
16	chr15:40986013..40988355-chr15:41045826..41048654,2	MCF-7	breast:
17	chr15:40950840..40952962-chr15:40970003..40972550,2	K562	blood:
18	chr15:40990811..40992810-chr15:41055825..41057654,2	MCF-7	breast:
19	chr15:40970986..40971527-chr15:41186009..41186918,2	K562	blood:
20	chr15:40984748..40990654-chr15:41044779..41050104,8	K562	blood:
21	chr15:40954350..40957294-chr15:40985826..40987543,2	K562	blood:
22	chr15:40970892..40971505-chr15:41074542..41075433,3	K562	blood:
23	chr15:40990437..40992433-chr15:41186523..41189273,2	K562	blood:
24	chr15:40985800..40990095-chr15:41055400..41057901,4	K562	blood:
25	chr1:33502049..33502864-chr15:40986870..40987564,2	Hela-S3	cervix:
26	chr15:40986558..40989601-chr15:40990368..40993764,9	K562	blood:
27	chr15:40987273..40988882-chr15:41061961..41063775,2	K562	blood:
28	chr15:40986478..40988882-chr15:41036813..41039846,3	K562	blood:
29	chr15:40984748..40987218-chr15:41046649..41049070,3	K562	blood:
30	chr15:40983418..40985214-chr15:40986954..40989432,2	K562	blood:
31	chr15:40987923..40990095-chr15:41055400..41057842,2	K562	blood:
32	chr15:40860821..40863087-chr15:40987318..40989233,3	K562	blood:
33	chr1:151964793..151965451-chr15:40986980..40987504,2	Hela-S3	cervix:
34	chr15:40953000..40955816-chr15:40958237..40959774,2	K562	blood:
35	chr15:40986981..40987821-chr3:44379041..44379997,2	Hela-S3	cervix:
36	chr15:40985310..40988262-chr15:41045857..41048554,2	MCF-7	breast:
37	chr15:40985078..40988247-chr15:41185737..41188201,3	K562	blood:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAM82A2-2	chr15:40979921-40980042	ENSG00000245849
2	lnc-FAM82A2-2	chr15:40986784-40986993	ENSG00000245849
3	lnc-FAM82A2-2	chr15:40986784-40986993	ENSG00000245849
4	lnc-FAM82A2-2	chr15:40987210-40987296	ENSG00000245849
5	lnc-FAM82A2-2	chr15:40978922-40979344	ENSG00000245849
6	lnc-FAM82A2-2	chr15:40987210-40987294	ENSG00000245849

No data

Variant related genes	Relation type
RAD51-AS1	TF binding region
RAD51	TF binding region
RAD51-AS1	CpG island
RAD51	CpG island
ENSG00000261183	chromatin interactions
ENSG00000004455	chromatin interactions
ENSG00000137880	chromatin interactions
ENSG00000188277	chromatin interactions
ENSG00000245849	chromatin interactions
ENSG00000104142	chromatin interactions
ENSG00000108654	chromatin interactions
ENSG00000166145	chromatin interactions
ENSG00000137824	chromatin interactions
ENSG00000204568	chromatin interactions
ENSG00000051180	chromatin interactions
ENSG00000197747	chromatin interactions
ENSG00000104129	chromatin interactions
ENSG00000137812	chromatin interactions
ENSG00000179152	chromatin interactions
ENSG00000204569	chromatin interactions
ENSG00000166133	chromatin interactions
ENSG00000247556	chromatin interactions
ENSG00000124357	chromatin interactions
ENSG00000258890	chromatin interactions
GRIA1	miRNA target sites
ABHD5	miRNA target sites
ZBTB33	miRNA target sites
TRPC3	miRNA target sites
LDLR	miRNA target sites

Extended variants
information (count: 1451 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:1451 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs35047458	chr15:40959624-40959625	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs555028961	chr15:40959629-40959630	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs139958902	chr15:40959633-40959634	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs74795419	chr15:40959643-40959644	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs113608153	chr15:40959653-40959654	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs557994315	chr15:40959654-40959655	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs76353224	chr15:40959666-40959667	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs570072051	chr15:40959667-40959668	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs563748117	chr15:40959673-40959674	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs529302737	chr15:40959694-40959695	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs151289815	chr15:40959737-40959738	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs543020330	chr15:40959741-40959742	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs373987473	chr15:40959872-40959873	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs149852499	chr15:40959954-40959955	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs115562891	chr15:40959983-40959984	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs551616670	chr15:40960003-40960004	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs571547314	chr15:40960018-40960019	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs569137866	chr15:40960019-40960020	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs549501549	chr15:40960053-40960054	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs569428187	chr15:40960071-40960072	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs376473634	chr15:40960124-40960125	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs535173559	chr15:40960148-40960149	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs183905473	chr15:40960163-40960164	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs140072678	chr15:40960165-40960166	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs116758434	chr15:40960169-40960170	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs558082695	chr15:40960185-40960186	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs113227023	chr15:40960193-40960194	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs566672318	chr15:40960256-40960257	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs533905538	chr15:40960272-40960273	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs543625215	chr15:40960301-40960302	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs147582424	chr15:40960304-40960305	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs574099179	chr15:40960323-40960324	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs187567477	chr15:40960363-40960364	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs542707977	chr15:40960364-40960365	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs559706379	chr15:40960369-40960370	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs370016260	chr15:40960392-40960393	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs8029530	chr15:40960402-40960403	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
38	rs75301886	chr15:40960404-40960405	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs200780012	chr15:40960412-40960413	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs376193269	chr15:40960423-40960424	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs531077935	chr15:40960426-40960427	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs191345130	chr15:40960428-40960429	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs12902568	chr15:40960432-40960433	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
44	rs528997165	chr15:40960442-40960443	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs548796293	chr15:40960447-40960448	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs182110015	chr15:40960461-40960462	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs79789155	chr15:40960486-40960487	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs79274407	chr15:40960492-40960493	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs571578253	chr15:40960511-40960512	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs537311348	chr15:40960544-40960545	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:68)

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
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
Ovarian cancer	22174824	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	17053054	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
lymphocytic leukemia	21291569	CNVD
Cancer	20164920	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Cancer	21129771	CNVD
Papillary thyroid carcinoma	22161024	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	21045282	CNVD
Breast cancer	22032731	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Multiple myeloma	16616336	CNVD
Renal cell carcinoma	18765545	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:991 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:40887800-40961600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
2	chr15:40913800-40986000	Weak transcription	A549	lung
3	chr15:40914400-40960000	Weak transcription	NHLF	lung
4	chr15:40943000-40971400	Weak transcription	Primary B cells from cord blood	blood
5	chr15:40945000-40984200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr15:40945200-40961400	Weak transcription	Placenta Amnion	Placenta Amnion
7	chr15:40946600-40959800	Weak transcription	Gastric	stomach
8	chr15:40950000-40981200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
9	chr15:40950200-40964200	Weak transcription	Osteobl	bone
10	chr15:40953000-40960200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr15:40953800-40960000	Weak transcription	Fetal Muscle Leg	muscle
12	chr15:40954600-40959800	Weak transcription	NHEK	skin
13	chr15:40954800-40960000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr15:40955200-40959800	Weak transcription	H1 Cell Line	embryonic stem cell
15	chr15:40955200-40961000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
16	chr15:40955200-40964400	Weak transcription	GM12878-XiMat	blood
17	chr15:40955200-40976600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
18	chr15:40955200-40983200	Weak transcription	Fetal Intestine Small	intestine
19	chr15:40955400-40960400	Weak transcription	Cortex derived primary cultured neurospheres	brain
20	chr15:40955800-40976000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
21	chr15:40956800-40960400	Weak transcription	Fetal Thymus	thymus
22	chr15:40956800-40963000	Weak transcription	Hela-S3	cervix
23	chr15:40956800-40966000	Weak transcription	Monocytes-CD14+_RO01746	blood
24	chr15:40956800-40971200	Weak transcription	Dnd41	blood
25	chr15:40957200-40960600	Weak transcription	Fetal Stomach	stomach
26	chr15:40957400-40959800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
27	chr15:40957400-40959800	Weak transcription	Primary monocytes fromperipheralblood	blood
28	chr15:40957600-40961400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
29	chr15:40958200-40960400	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
30	chr15:40958400-40960000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr15:40958400-40966600	Weak transcription	Primary neutrophils fromperipheralblood	blood
32	chr15:40958600-40960600	Weak transcription	Fetal Muscle Trunk	muscle
33	chr15:40958600-40981000	Weak transcription	Thymus	Thymus
34	chr15:40959000-40961800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
35	chr15:40959600-40959800	Enhancers	Liver	Liver
36	chr15:40960400-40977000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
37	chr15:40964400-40965200	Enhancers	Primary B cells from peripheral blood	blood
38	chr15:40964400-40965400	Enhancers	GM12878-XiMat	blood
39	chr15:40968000-40968400	Enhancers	HepG2	liver
40	chr15:40968400-40971200	Weak transcription	HepG2	liver
41	chr15:40971000-40971200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
42	chr15:40971000-40971400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
43	chr15:40971000-40971400	Enhancers	Hela-S3	cervix
44	chr15:40971200-40971400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
45	chr15:40971200-40971400	Enhancers	Brain Angular Gyrus	brain
46	chr15:40971200-40971400	Enhancers	Brain Hippocampus Middle	brain
47	chr15:40971200-40971400	Enhancers	HepG2	liver
48	chr15:40971200-40971600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
49	chr15:40971200-40971600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
50	chr15:40971200-40971600	Enhancers	Primary T killer memory cells from peripheral blood	blood

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