Variant report

Variant	nsv904071
Chromosome Location	chr15:35150897-35250771
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:471)
CpG islands
(count:183)
Chromatin interactive
region (count:41)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:471 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:35212450-35212797	K562	blood:	n/a	n/a
2	ARID3A	chr15:35184857-35184898	K562	blood:	n/a	n/a
3	ARID3A	chr15:35196884-35197044	K562	blood:	n/a	n/a
4	ATF1	chr15:35171354-35171720	K562	blood:	n/a	n/a
5	ATF1	chr15:35196859-35197041	K562	blood:	n/a	n/a
6	BACH1	chr15:35196895-35197060	K562	blood:	n/a	n/a
7	BATF	chr15:35245966-35246207	GM12878	blood:	n/a	chr15:35246068-35246079
8	BHLHE40	chr15:35212513-35212769	GM12878	blood:	n/a	n/a
9	BRCA1	chr15:35212474-35212765	H1-hESC	embryonic stem cell:	n/a	n/a
10	CBX3	chr15:35185193-35185519	K562	blood:	n/a	n/a
11	CBX3	chr15:35185150-35185569	K562	blood:	n/a	n/a
12	CEBPB	chr15:35196797-35197091	K562	blood:	n/a	n/a
13	CEBPB	chr15:35250582-35250873	K562	blood:	n/a	chr15:35250719-35250728 chr15:35250719-35250728 chr15:35250719-35250728 chr15:35250717-35250728 chr15:35250718-35250729 chr15:35250725-35250738 chr15:35250717-35250730 chr15:35250719-35250728
14	CEBPB	chr15:35231929-35232235	A549	lung:	n/a	chr15:35232072-35232083
15	CEBPB	chr15:35171204-35171255	H1-hESC	embryonic stem cell:	n/a	n/a
16	CEBPB	chr15:35172697-35173042	A549	lung:	n/a	n/a
17	CEBPB	chr15:35212431-35212756	A549	lung:	n/a	n/a
18	CEBPB	chr15:35181802-35182022	K562	blood:	n/a	n/a
19	CEBPB	chr15:35181766-35182108	IMR90	lung:	n/a	n/a
20	CEBPB	chr15:35250585-35250899	Hela-S3	cervix:	n/a	chr15:35250719-35250728 chr15:35250719-35250728 chr15:35250719-35250728 chr15:35250717-35250728 chr15:35250718-35250729 chr15:35250725-35250738 chr15:35250717-35250730 chr15:35250719-35250728
21	CEBPB	chr15:35172718-35173042	IMR90	lung:	n/a	n/a
22	CEBPB	chr15:35244484-35244789	A549	lung:	n/a	chr15:35244640-35244651
23	CEBPB	chr15:35181740-35182097	ECC-1	luminal epithelium:	n/a	n/a
24	CEBPB	chr15:35250671-35250802	H1-hESC	embryonic stem cell:	n/a	chr15:35250719-35250728 chr15:35250719-35250728 chr15:35250719-35250728 chr15:35250717-35250728 chr15:35250718-35250729 chr15:35250725-35250738 chr15:35250717-35250730 chr15:35250719-35250728
25	CEBPB	chr15:35250563-35250821	IMR90	lung:	n/a	chr15:35250719-35250728 chr15:35250719-35250728 chr15:35250719-35250728 chr15:35250717-35250728 chr15:35250718-35250729 chr15:35250725-35250738 chr15:35250717-35250730 chr15:35250719-35250728
26	CEBPB	chr15:35181820-35182060	ECC-1	luminal epithelium:	n/a	n/a
27	CEBPB	chr15:35219922-35220213	A549	lung:	n/a	n/a
28	CEBPB	chr15:35181760-35182127	A549	lung:	n/a	n/a
29	CEBPB	chr15:35244481-35244793	Hela-S3	cervix:	n/a	chr15:35244640-35244651
30	CEBPB	chr15:35250547-35250897	HepG2	liver:	n/a	chr15:35250719-35250728 chr15:35250719-35250728 chr15:35250719-35250728 chr15:35250717-35250728 chr15:35250718-35250729 chr15:35250725-35250738 chr15:35250717-35250730 chr15:35250719-35250728
31	CEBPB	chr15:35172713-35173056	HepG2	liver:	n/a	n/a
32	CEBPB	chr15:35244487-35244733	HepG2	liver:	n/a	chr15:35244640-35244651
33	CEBPB	chr15:35172732-35173004	K562	blood:	n/a	n/a
34	CEBPB	chr15:35231938-35232226	HepG2	liver:	n/a	chr15:35232072-35232083
35	CEBPB	chr15:35249146-35249303	A549	lung:	n/a	chr15:35249229-35249238
36	CEBPB	chr15:35181776-35182069	Hela-S3	cervix:	n/a	n/a
37	CEBPB	chr15:35181666-35182230	A549	lung:	n/a	n/a
38	CEBPB	chr15:35250546-35250885	A549	lung:	n/a	chr15:35250719-35250728 chr15:35250719-35250728 chr15:35250719-35250728 chr15:35250717-35250728 chr15:35250718-35250729 chr15:35250725-35250738 chr15:35250717-35250730 chr15:35250719-35250728
39	CEBPB	chr15:35181786-35182057	A549	lung:	n/a	n/a
40	CHD1	chr15:35185174-35185188	H1-hESC	embryonic stem cell:	n/a	n/a
41	CHD2	chr15:35185306-35185917	H1-hESC	embryonic stem cell:	n/a	n/a
42	CTCF	chr15:35212520-35212670	HUVEC	blood vessel:	n/a	n/a
43	CTCF	chr15:35182375-35182474	GM12878	blood:	n/a	n/a
44	CTCF	chr15:35212540-35212690	GM12878	blood:	n/a	n/a
45	CTCF	chr15:35212580-35212730	HCT-116	colon:	n/a	n/a
46	CTCF	chr15:35212498-35212745	LNCaP	prostate:	n/a	n/a
47	CTCF	chr15:35212620-35212770	NHLF	lung:	n/a	n/a
48	CTCF	chr15:35212501-35212744	K562	blood:	n/a	n/a
49	CTCF	chr15:35212540-35212690	SK-N-SH_RA	brain:	n/a	n/a
50	CTCF	chr15:35212560-35212710	HEEpiC	esophagus:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:35178803-35178853	AG04450	lung:	fetal
2	chr15:35178803-35178853	U87	brain:	n/a
3	chr15:35178803-35178853	HEK293	kidney:	embryo
4	chr15:35238599-35238649	BE2_C	brain:	n/a
5	chr15:35238599-35238649	HRCEpiC	kidney:	n/a
6	chr15:35202392-35202442	ProgFib	skin:	n/a
7	chr15:35178803-35178853	IMR90	lung:	fetal
8	chr15:35202392-35202442	HIPEpiC	eye:	n/a
9	chr15:35178803-35178853	HRE	kidney:	n/a
10	chr15:35202392-35202442	ECC-1	luminal epithelium:	n/a
11	chr15:35202392-35202442	LNCaP	prostate:	n/a
12	chr15:35202392-35202442	Jurkat	blood:	n/a
13	chr15:35178803-35178853	A549	lung:	n/a
14	chr15:35238599-35238649	AG09309	skin:	n/a
15	chr15:35178803-35178853	AoSMC	blood vessel:	n/a
16	chr15:35238599-35238649	HCPEpiC	choroid plexus:	n/a
17	chr15:35178803-35178853	GM12892	blood:	n/a
18	chr15:35178803-35178853	GM12891	blood:	n/a
19	chr15:35178803-35178853	PANC-1	pancreas:	n/a
20	chr15:35178803-35178853	HIPEpiC	eye:	n/a
21	chr15:35238599-35238649	NB4	blood:	n/a
22	chr15:35202392-35202442	AG04450	lung:	fetal
23	chr15:35238599-35238649	ProgFib	skin:	n/a
24	chr15:35202392-35202442	HCF	heart:	n/a
25	chr15:35202392-35202442	A549	lung:	n/a
26	chr15:35178803-35178853	AG04449	skin:	fetal
27	chr15:35178803-35178853	AG09319	gingival:	n/a
28	chr15:35202392-35202442	CMK	blood:	n/a
29	chr15:35178803-35178853	Jurkat	blood:	n/a
30	chr15:35238599-35238649	HPAEpiC	pulmonary alveolar:	n/a
31	chr15:35178803-35178853	NB4	blood:	n/a
32	chr15:35178803-35178853	ECC-1	luminal epithelium:	n/a
33	chr15:35238599-35238649	BJ	skin:	n/a
34	chr15:35202392-35202442	T-47D	breast:	n/a
35	chr15:35178803-35178853	RPTEC	kidney:	n/a
36	chr15:35178803-35178853	SK-N-MC	brain:	n/a
37	chr15:35202392-35202442	AG10803	skin:	n/a
38	chr15:35202392-35202442	IMR90	lung:	fetal
39	chr15:35202392-35202442	HMEC	breast:	n/a
40	chr15:35202392-35202442	PFSK-1	brain:	n/a
41	chr15:35238599-35238649	GM19239	blood:	n/a
42	chr15:35238599-35238649	AG04450	lung:	fetal
43	chr15:35178803-35178853	ovcar-3	ovarian:	n/a
44	chr15:35238599-35238649	LNCaP	prostate:	n/a
45	chr15:35238599-35238649	ovcar-3	ovarian:	n/a
46	chr15:35178803-35178853	HRCEpiC	kidney:	n/a
47	chr15:35238599-35238649	HRPEpiC	eye:	n/a
48	chr15:35238599-35238649	A549	lung:	n/a
49	chr15:35178803-35178853	HEEpiC	esophagus:	n/a
50	chr15:35202392-35202442	HEEpiC	esophagus:	n/a

(count:41 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:35199285..35200789-chr15:35201669..35204219,2	K562	blood:
2	chr15:35198651..35201621-chr15:35206696..35208281,2	K562	blood:
3	chr15:35151497..35153844-chr15:35156867..35158791,2	K562	blood:
4	chr15:35241441..35242954-chr15:35249082..35251825,2	K562	blood:
5	chr15:35169980..35173467-chr15:35175029..35177005,3	K562	blood:
6	chr15:35169980..35173467-chr15:35175029..35177005,3	K562	blood:
7	chr15:34913918..34914531-chr15:35212584..35213285,2	MCF-7	breast:
8	chr15:35195184..35198331-chr15:35198423..35200783,3	K562	blood:
9	chr15:35159789..35161996-chr15:35162346..35164521,2	K562	blood:
10	chr15:35211074..35213644-chr15:35214975..35217514,2	K562	blood:
11	chr15:35249955..35252254-chr15:35836520..35838863,2	K562	blood:
12	chr15:34879228..34880933-chr15:35174696..35177534,2	K562	blood:
13	chr15:35169980..35172331-chr15:35175029..35176671,2	K562	blood:
14	chr15:35189106..35191007-chr15:35202848..35205608,2	K562	blood:
15	chr15:35162821..35165306-chr15:35168208..35170309,3	K562	blood:
16	chr15:35187656..35189304-chr15:35193173..35195571,2	K562	blood:
17	chr15:35193071..35194690-chr15:35201622..35203662,2	K562	blood:
18	chr15:35187656..35189304-chr15:35193173..35195571,2	K562	blood:
19	chr15:35193071..35194690-chr15:35201622..35203662,2	K562	blood:
20	chr15:35243309..35245950-chr15:35248487..35252213,3	K562	blood:
21	chr15:35199285..35200789-chr15:35201669..35204219,2	K562	blood:
22	chr15:35151497..35153844-chr15:35156867..35158791,2	K562	blood:
23	chr15:34949750..34952665-chr15:35241317..35244101,2	K562	blood:
24	chr15:35219148..35220809-chr15:35259856..35261653,2	K562	blood:
25	chr15:34953489..34955951-chr15:35181219..35183157,2	K562	blood:
26	chr15:35189106..35191007-chr15:35202848..35205608,2	K562	blood:
27	chr15:35241742..35244149-chr15:35278912..35280848,3	K562	blood:
28	chr15:34908586..34909269-chr15:35212549..35213068,2	MCF-7	breast:
29	chr15:34908560..34909558-chr15:35212164..35213076,4	K562	blood:
30	chr15:35243510..35246015-chr15:35255184..35256864,2	K562	blood:
31	chr15:35211074..35213644-chr15:35214975..35217514,2	K562	blood:
32	chr15:35243309..35245950-chr15:35248487..35252213,3	K562	blood:
33	chr15:35195184..35198331-chr15:35198423..35200783,3	K562	blood:
34	chr15:34913751..34914597-chr15:35212096..35212867,7	K562	blood:
35	chr15:35198651..35201621-chr15:35206696..35208281,2	K562	blood:
36	chr15:35241441..35242954-chr15:35249082..35251825,2	K562	blood:
37	chr15:35202607..35205491-chr15:35208140..35210817,2	K562	blood:
38	chr15:35202607..35205491-chr15:35208140..35210817,2	K562	blood:
39	chr13:52023403..52026177-chr15:35180246..35182636,2	MCF-7	breast:
40	chr15:35162821..35165306-chr15:35168208..35170309,3	K562	blood:
41	chr15:35169980..35172331-chr15:35175029..35176671,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ACTC1-1	chr15:35160323-35160538	expReg_chr15_1403_-

No data

Variant related genes	Relation type
AQR	TF binding region
ENSG00000231409	TF binding region
AQR	CpG island
ENSG00000231409	CpG island
ENSG00000248079	chromatin interactions
ENSG00000134146	chromatin interactions
ENSG00000102786	chromatin interactions
ENSG00000215252	chromatin interactions
ENSG00000021776	chromatin interactions
ENSG00000198146	chromatin interactions

Extended variants
information (count: 3600 )
Associated
traits (count: 69 )

Variant overlapped rSNPs/rCNVs (count:3600 , 50 per page) page: 1 2 3 4 5 6 7 ... 72

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4923806	chr15:35150897-35150898	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs528909502	chr15:35150949-35150950	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs145115598	chr15:35150989-35150990	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs555067158	chr15:35150997-35150998	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs147569536	chr15:35151025-35151026	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs79353570	chr15:35151043-35151044	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs549867610	chr15:35151044-35151045	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs553031822	chr15:35151057-35151058	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs577877705	chr15:35151068-35151069	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs544855990	chr15:35151077-35151078	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs185230443	chr15:35151081-35151082	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs189601678	chr15:35151128-35151129	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs146915250	chr15:35151156-35151157	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs79185347	chr15:35151183-35151184	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs561014702	chr15:35151226-35151227	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs181822862	chr15:35151243-35151244	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs528728881	chr15:35151256-35151257	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs112552288	chr15:35151263-35151264	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs186858642	chr15:35151282-35151283	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs532861969	chr15:35151285-35151286	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs551267474	chr15:35151291-35151292	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs72717427	chr15:35151293-35151294	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs569290656	chr15:35151308-35151309	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs4497641	chr15:35151357-35151358	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs151328358	chr15:35151373-35151374	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs140577786	chr15:35151394-35151395	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs533995511	chr15:35151421-35151422	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs553135058	chr15:35151426-35151427	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs111255988	chr15:35151438-35151439	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs191650151	chr15:35151443-35151444	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs113642838	chr15:35151474-35151475	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs574919482	chr15:35151517-35151518	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs138252163	chr15:35151544-35151545	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs572371143	chr15:35151546-35151547	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs554410420	chr15:35151550-35151551	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs572906996	chr15:35151630-35151631	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs35987265	chr15:35151697-35151698	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs539905020	chr15:35151807-35151808	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs115539624	chr15:35151847-35151848	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs567664448	chr15:35151859-35151860	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs577927600	chr15:35151878-35151879	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs532719005	chr15:35151897-35151898	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs142884941	chr15:35151913-35151914	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs113084339	chr15:35151931-35151932	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs138836421	chr15:35151973-35151974	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs530155537	chr15:35151997-35151998	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs76299506	chr15:35152017-35152018	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs146289069	chr15:35152039-35152040	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs527806917	chr15:35152041-35152042	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs552352906	chr15:35152043-35152044	Weak transcription Strong transcription	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
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
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
Cancer	20164920	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:3014 , 50 per page) page: 1 2 3 4 5 6 7 ... 61

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:35140400-35221600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr15:35141600-35154800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr15:35141800-35153400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr15:35142600-35153400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
5	chr15:35142600-35156400	Weak transcription	Lung	lung
6	chr15:35142600-35180200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr15:35142600-35185200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
8	chr15:35145000-35155400	Strong transcription	Primary T cells from cord blood	blood
9	chr15:35145200-35198200	Weak transcription	Colonic Mucosa	Colon
10	chr15:35145600-35152000	Strong transcription	Fetal Muscle Trunk	muscle
11	chr15:35145600-35161200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr15:35145600-35184600	Strong transcription	Monocytes-CD14+_RO01746	blood
13	chr15:35145800-35153000	Weak transcription	Left Ventricle	heart
14	chr15:35145800-35185400	Weak transcription	Psoas Muscle	Psoas
15	chr15:35146400-35156600	Strong transcription	Rectal Mucosa Donor 31	rectum
16	chr15:35146400-35175400	Weak transcription	Small Intestine	intestine
17	chr15:35146600-35155600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
18	chr15:35146600-35160400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
19	chr15:35146600-35160800	Strong transcription	Primary B cells from cord blood	blood
20	chr15:35146600-35184800	Strong transcription	Primary T helper cells fromperipheralblood	blood
21	chr15:35146600-35185200	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
22	chr15:35146800-35155200	Strong transcription	Sigmoid Colon	Sigmoid Colon
23	chr15:35146800-35158000	Strong transcription	Primary neutrophils fromperipheralblood	blood
24	chr15:35146800-35159000	Strong transcription	Primary T helper cells PMA-I stimulated	--
25	chr15:35146800-35161200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
26	chr15:35146800-35183200	Strong transcription	Primary B cells from peripheral blood	blood
27	chr15:35146800-35185200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
28	chr15:35146800-35185200	Strong transcription	Primary monocytes fromperipheralblood	blood
29	chr15:35147000-35155800	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr15:35147000-35157800	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
31	chr15:35147000-35161400	Strong transcription	HUES64 Cell Line	embryonic stem cell
32	chr15:35147000-35168200	Strong transcription	HUES48 Cell Line	embryonic stem cell
33	chr15:35147200-35152600	Strong transcription	iPS-18 Cell Line	embryonic stem cell
34	chr15:35147200-35155200	Strong transcription	Rectal Mucosa Donor 29	rectum
35	chr15:35147200-35155800	Strong transcription	Dnd41	blood
36	chr15:35147200-35162000	Strong transcription	HUES6 Cell Line	embryonic stem cell
37	chr15:35147200-35163600	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
38	chr15:35147400-35151800	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
39	chr15:35147400-35152000	Strong transcription	Duodenum Mucosa	Duodenum
40	chr15:35147400-35155400	Strong transcription	Primary T cells fromperipheralblood	blood
41	chr15:35147400-35155800	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
42	chr15:35147600-35160800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
43	chr15:35147600-35161200	Weak transcription	Right Ventricle	heart
44	chr15:35147800-35152000	Strong transcription	GM12878-XiMat	blood
45	chr15:35147800-35155400	Strong transcription	iPS-20b Cell Line	embryonic stem cell
46	chr15:35148000-35158200	Strong transcription	Placenta	Placenta
47	chr15:35148200-35153400	Weak transcription	Fetal Brain Male	brain
48	chr15:35148200-35161200	Weak transcription	Pancreatic Islets	Pancreatic Islet
49	chr15:35148200-35185400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
50	chr15:35148400-35151200	Weak transcription	HSMMtube	muscle

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