Variant report

Variant	nsv542369
Chromosome Location	chr15:43237103-43385515
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:390)
CpG islands
(count:62)
Chromatin interactive
region (count:54)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:390 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:43266377-43266999	HepG2	liver:	n/a	n/a
2	ARID3A	chr15:43264010-43264447	HepG2	liver:	n/a	n/a
3	ATF1	chr15:43249174-43249360	K562	blood:	n/a	n/a
4	ATF2	chr15:43378722-43379113	GM12878	blood:	n/a	n/a
5	BACH1	chr15:43249047-43249355	K562	blood:	n/a	n/a
6	BACH1	chr15:43300070-43300234	K562	blood:	n/a	n/a
7	BATF	chr15:43378535-43379134	GM12878	blood:	n/a	n/a
8	BATF	chr15:43378759-43379062	GM12878	blood:	n/a	n/a
9	BATF	chr15:43359977-43360156	GM12878	blood:	n/a	n/a
10	BATF	chr15:43359931-43360160	GM12878	blood:	n/a	n/a
11	BATF	chr15:43317425-43317631	GM12878	blood:	n/a	chr15:43317546-43317557
12	BATF	chr15:43317398-43317616	GM12878	blood:	n/a	chr15:43317546-43317557
13	BCL11A	chr15:43368163-43368349	GM12878	blood:	n/a	n/a
14	BHLHE40	chr15:43271357-43271588	HepG2	liver:	n/a	n/a
15	BHLHE40	chr15:43382873-43382875	GM12878	blood:	n/a	n/a
16	CBX3	chr15:43248812-43249305	K562	blood:	n/a	n/a
17	CCNT2	chr15:43249078-43249284	K562	blood:	n/a	n/a
18	CEBPB	chr15:43264030-43264391	HepG2	liver:	n/a	n/a
19	CEBPB	chr15:43374731-43375035	A549	lung:	n/a	chr15:43374901-43374912
20	CEBPB	chr15:43360281-43360994	K562	blood:	n/a	n/a
21	CEBPB	chr15:43361465-43361481	K562	blood:	n/a	n/a
22	CEBPB	chr15:43360402-43360494	A549	lung:	n/a	n/a
23	CEBPB	chr15:43339371-43339585	HepG2	liver:	n/a	chr15:43339452-43339463
24	CEBPB	chr15:43374726-43375076	IMR90	lung:	n/a	chr15:43374901-43374912
25	CEBPB	chr15:43267428-43267668	K562	blood:	n/a	chr15:43267510-43267521
26	CEBPB	chr15:43378345-43378379	K562	blood:	n/a	n/a
27	CEBPB	chr15:43360300-43360568	K562	blood:	n/a	n/a
28	CEBPB	chr15:43249025-43249277	A549	lung:	n/a	chr15:43249128-43249139
29	CEBPB	chr15:43266573-43267048	HepG2	liver:	n/a	chr15:43266862-43266873
30	CEBPB	chr15:43385042-43385536	IMR90	lung:	n/a	chr15:43385335-43385347 chr15:43385107-43385118 chr15:43385105-43385118
31	CEBPB	chr15:43286806-43287085	IMR90	lung:	n/a	n/a
32	CEBPB	chr15:43264076-43264293	HepG2	liver:	n/a	n/a
33	CEBPB	chr15:43276857-43276941	A549	lung:	n/a	n/a
34	CEBPB	chr15:43366110-43366257	HepG2	liver:	n/a	chr15:43366175-43366186
35	CEBPB	chr15:43248951-43249305	IMR90	lung:	n/a	chr15:43249128-43249139
36	CEBPB	chr15:43264094-43264223	HepG2	liver:	n/a	n/a
37	CEBPB	chr15:43360298-43360558	IMR90	lung:	n/a	n/a
38	CEBPB	chr15:43247691-43248037	IMR90	lung:	n/a	n/a
39	CEBPB	chr15:43374726-43375081	HepG2	liver:	n/a	chr15:43374901-43374912
40	CEBPB	chr15:43249016-43249230	HepG2	liver:	n/a	chr15:43249128-43249139
41	CEBPB	chr15:43381521-43381833	H1-hESC	embryonic stem cell:	n/a	n/a
42	CEBPB	chr15:43366074-43366271	A549	lung:	n/a	chr15:43366175-43366186
43	CEBPB	chr15:43360329-43360596	Hela-S3	cervix:	n/a	n/a
44	CEBPB	chr15:43271342-43271649	Hela-S3	cervix:	n/a	chr15:43271432-43271443
45	CEBPB	chr15:43360346-43360517	H1-hESC	embryonic stem cell:	n/a	n/a
46	CEBPB	chr15:43248943-43249282	K562	blood:	n/a	chr15:43249128-43249139
47	CEBPB	chr15:43267389-43267577	IMR90	lung:	n/a	chr15:43267510-43267521
48	CEBPB	chr15:43366085-43366279	IMR90	lung:	n/a	chr15:43366175-43366186
49	CEBPB	chr15:43267403-43267611	HepG2	liver:	n/a	chr15:43267510-43267521
50	CEBPB	chr15:43275761-43275871	HepG2	liver:	n/a	chr15:43275813-43275824

(count:62 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:43297145-43297195	AG04450	lung:	fetal
2	chr15:43297145-43297195	AG04450	lung:	fetal
3	chr15:43297145-43297195	LNCaP	prostate:	n/a
4	chr15:43297145-43297195	IMR90	lung:	fetal
5	chr15:43297145-43297195	HNPCEpiC	eye:	n/a
6	chr15:43297145-43297195	H1-hESC	embryonic stem cell:	embryo
7	chr15:43297145-43297195	SK-N-SH_RA	brain:	n/a
8	chr15:43297145-43297195	BJ	skin:	n/a
9	chr15:43297145-43297195	HRCEpiC	kidney:	n/a
10	chr15:43297145-43297195	HMEC	breast:	n/a
11	chr15:43297145-43297195	Hepatocyte	liver:	n/a
12	chr15:43297145-43297195	SK-N-SH	brain:	n/a
13	chr15:43297145-43297195	GM19239	blood:	n/a
14	chr15:43297145-43297195	HEK293	kidney:	embryo
15	chr15:43297145-43297195	U87	brain:	n/a
16	chr15:43297145-43297195	ECC-1	luminal epithelium:	n/a
17	chr15:43297145-43297195	GM12892	blood:	n/a
18	chr15:43297145-43297195	Jurkat	blood:	n/a
19	chr15:43297145-43297195	HIPEpiC	eye:	n/a
20	chr15:43297145-43297195	MCF10A-Er-Src	breast:	n/a
21	chr15:43297145-43297195	SAEC	small airway:	n/a
22	chr15:43297145-43297195	K562	blood:	n/a
23	chr15:43297145-43297195	CMK	blood:	n/a
24	chr15:43297145-43297195	AoSMC	blood vessel:	n/a
25	chr15:43297145-43297195	GM12891	blood:	n/a
26	chr15:43297145-43297195	HepG2	liver:	n/a
27	chr15:43297145-43297195	PANC-1	pancreas:	n/a
28	chr15:43297145-43297195	PrEC	prostate:	n/a
29	chr15:43297145-43297195	HPAEpiC	pulmonary alveolar:	n/a
30	chr15:43297145-43297195	HCF	heart:	n/a
31	chr15:43297145-43297195	HCT-116	colon:	n/a
32	chr15:43297145-43297195	RPTEC	kidney:	n/a
33	chr15:43297145-43297195	NT2-D1	testis:	n/a
34	chr15:43297145-43297195	A549	lung:	n/a
35	chr15:43297145-43297195	PFSK-1	brain:	n/a
36	chr15:43297145-43297195	NH-A	brain:	n/a
37	chr15:43297145-43297195	GM12878	blood:	n/a
38	chr15:43297145-43297195	HCM	heart:	n/a
39	chr15:43297145-43297195	NHDF-neo	bronchial:	n/a
40	chr15:43297145-43297195	T-47D	breast:	n/a
41	chr15:43297145-43297195	HEEpiC	esophagus:	n/a
42	chr15:43297145-43297195	SKMC	muscle:	n/a
43	chr15:43297145-43297195	HRPEpiC	eye:	n/a
44	chr15:43297145-43297195	AG10803	skin:	n/a
45	chr15:43297145-43297195	GM06990	blood:	n/a
46	chr15:43297145-43297195	NB4	blood:	n/a
47	chr15:43297145-43297195	ovcar-3	ovarian:	n/a
48	chr15:43297145-43297195	SK-N-MC	brain:	n/a
49	chr15:43297145-43297195	HUVEC	blood vessel:	n/a
50	chr15:43297145-43297195	MCF-7	breast:	n/a

(count:54 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr15:43327543..43330321-chr15:43334414..43337253,2	MCF-7	breast:
2	chr15:43285221..43287358-chr15:43299885..43302016,2	K562	blood:
3	chr15:43277125..43279751-chr15:43281410..43283345,2	K562	blood:
4	chr15:43354633..43356543-chr15:43359222..43361458,2	K562	blood:
5	chr15:43274336..43276326-chr15:43276849..43278909,2	K562	blood:
6	chr15:43234709..43237589-chr15:43247590..43250522,2	MCF-7	breast:
7	chr15:43246670..43249589-chr15:43250577..43252629,2	K562	blood:
8	chr15:43227976..43230941-chr15:43258410..43260187,2	K562	blood:
9	chr15:43274336..43276326-chr15:43276849..43278909,2	K562	blood:
10	chr15:43356222..43358202-chr15:43362263..43364733,2	MCF-7	breast:
11	chr15:43325373..43328292-chr15:43334536..43336063,2	K562	blood:
12	chr15:43325373..43328292-chr15:43334536..43336063,2	K562	blood:
13	chr15:43346995..43348533-chr15:43350036..43351977,2	K562	blood:
14	chr15:43385287..43387946-chr15:43396303..43398701,2	K562	blood:
15	chr15:43375936..43379231-chr15:43382227..43385005,3	K562	blood:
16	chr15:43368519..43371458-chr15:43478469..43480102,2	K562	blood:
17	chr15:43292761..43295218-chr15:43297989..43300121,2	K562	blood:
18	chr15:43346995..43348533-chr15:43350036..43351977,2	K562	blood:
19	chr15:43283254..43285115-chr15:43286974..43289576,2	K562	blood:
20	chr15:43246670..43249589-chr15:43250577..43252629,2	K562	blood:
21	chr15:43234809..43237372-chr15:43248299..43250757,2	K562	blood:
22	chr15:43234709..43237589-chr15:43247590..43250522,2	MCF-7	breast:
23	chr15:43017657..43020242-chr15:43257370..43259686,2	K562	blood:
24	chr15:43306847..43311067-chr15:43312226..43316473,3	K562	blood:
25	chr15:43356222..43358202-chr15:43362263..43364733,2	MCF-7	breast:
26	chr15:43025909..43027534-chr15:43242943..43244599,2	K562	blood:
27	chr15:43277125..43279751-chr15:43281410..43283345,2	K562	blood:
28	chr15:43278687..43281856-chr15:43291013..43293652,3	K562	blood:
29	chr15:43242538..43245839-chr15:43247604..43251014,3	K562	blood:
30	chr15:43379754..43382277-chr15:43415120..43416972,2	K562	blood:
31	chr15:43354633..43356543-chr15:43359222..43361458,2	K562	blood:
32	chr15:43360121..43362777-chr15:43399326..43401275,2	MCF-7	breast:
33	chr15:43234809..43237372-chr15:43248299..43250757,2	K562	blood:
34	chr15:43292761..43295218-chr15:43297989..43300121,2	K562	blood:
35	chr15:43282136..43285343-chr15:43291276..43293438,3	K562	blood:
36	chr15:43278687..43281856-chr15:43291013..43293652,3	K562	blood:
37	chr15:43283254..43285115-chr15:43286974..43289576,2	K562	blood:
38	chr15:43283018..43285343-chr15:43291276..43293330,3	K562	blood:
39	chr15:43360392..43362682-chr15:43423469..43425924,2	K562	blood:
40	chr15:43337776..43340565-chr15:43396734..43398497,2	K562	blood:
41	chr15:43336054..43338771-chr15:43342997..43344575,2	MCF-7	breast:
42	chr15:43375936..43379231-chr15:43382227..43385005,3	K562	blood:
43	chr15:43282136..43285343-chr15:43291276..43293438,3	K562	blood:
44	chr15:43336054..43338771-chr15:43342997..43344575,2	MCF-7	breast:
45	chr15:43285221..43287358-chr15:43299885..43302016,2	K562	blood:
46	chr15:43326792..43329076-chr15:43333977..43336036,2	K562	blood:
47	chr15:43339146..43340895-chr15:43431393..43434266,2	K562	blood:
48	chr15:43383221..43385892-chr15:43389653..43392510,3	K562	blood:
49	chr15:43283018..43285343-chr15:43291276..43293330,3	K562	blood:
50	chr15:43326792..43329076-chr15:43333977..43336036,2	K562	blood:

No data

Variant related genes	Relation type
UBR1	TF binding region
FDPSP4	TF binding region
UBR1	CpG island
FDPSP4	CpG island
ENSG00000159459	chromatin interactions
ENSG00000137842	chromatin interactions
ENSG00000140326	chromatin interactions

Extended variants
information (count: 5050 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:5050 , 50 per page) page: 1 2 3 4 5 6 7 ... 101

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs550997551	chr15:43237146-43237147	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs186367729	chr15:43237184-43237185	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs3803341	chr15:43237203-43237204	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
4	rs567207121	chr15:43237276-43237277	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs367590102	chr15:43237280-43237281	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs573405874	chr15:43237321-43237322	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs77199172	chr15:43237325-43237326	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs111236961	chr15:43237340-43237341	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs539188547	chr15:43237403-43237404	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs62020698	chr15:43237414-43237415	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs191274063	chr15:43237436-43237437	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs544900568	chr15:43237441-43237442	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs372216394	chr15:43237457-43237458	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs182619531	chr15:43237493-43237494	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs373737770	chr15:43237509-43237510	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs145216577	chr15:43237530-43237531	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs201714735	chr15:43237532-43237533	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs149137306	chr15:43237564-43237565	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs375516146	chr15:43237569-43237570	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs16957277	chr15:43237572-43237573	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs139367236	chr15:43237575-43237576	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs201159906	chr15:43237631-43237632	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs141828250	chr15:43237642-43237643	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs372344407	chr15:43237676-43237677	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs532187057	chr15:43237690-43237691	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs376915685	chr15:43237695-43237696	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs151182256	chr15:43237740-43237741	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs183160602	chr15:43237748-43237749	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs147169390	chr15:43237769-43237770	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs568348638	chr15:43237770-43237771	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs548170458	chr15:43237782-43237783	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs11352938	chr15:43237806-43237807	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs386783495	chr15:43237809-43237810	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs201058812	chr15:43237810-43237811	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs138077177	chr15:43237812-43237813	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs79570742	chr15:43237814-43237815	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs58543903	chr15:43237818-43237819	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs201642575	chr15:43237823-43237824	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs538427024	chr15:43237879-43237880	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs534164417	chr15:43237892-43237893	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs567663455	chr15:43237940-43237941	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs553881584	chr15:43237976-43237977	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs536223483	chr15:43237998-43237999	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs547074350	chr15:43238046-43238047	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs78824768	chr15:43238081-43238082	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs141221615	chr15:43238122-43238123	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs559224922	chr15:43238127-43238128	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs187888953	chr15:43238156-43238157	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs538547735	chr15:43238196-43238197	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs554939286	chr15:43238206-43238207	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:70)

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
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
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
Renal cell carcinoma	18765545	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	16272173	CNVD
Hepatocellular carcinoma	16750200	CNVD
Abnormal phenotypes	18644119	CNVD
Cancer	16751803	CNVD
Cancer	20164919	CNVD
Pancreatic cancer	17952125	CNVD
Melanoma	20877625	CNVD
Renal cell carcinoma	21215367	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Intellectual disability	21811512	CNVD

Chromatin state (count:4445 , 50 per page) page: 1 2 3 4 5 6 7 ... 89

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:43223600-43238400	Weak transcription	Ovary	ovary
2	chr15:43225800-43247600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
3	chr15:43226000-43242200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
4	chr15:43228200-43237200	Weak transcription	NHEK	skin
5	chr15:43228200-43242400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
6	chr15:43229200-43237400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
7	chr15:43229800-43237400	Weak transcription	Brain Germinal Matrix	brain
8	chr15:43230000-43237400	Weak transcription	HSMMtube	muscle
9	chr15:43230200-43237200	Weak transcription	Stomach Smooth Muscle	stomach
10	chr15:43230200-43237400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
11	chr15:43230200-43237400	Weak transcription	Thymus	Thymus
12	chr15:43230200-43242400	Weak transcription	NHLF	lung
13	chr15:43230400-43237600	Weak transcription	Lung	lung
14	chr15:43230600-43237400	Weak transcription	Aorta	Aorta
15	chr15:43230600-43238400	Weak transcription	Fetal Intestine Small	intestine
16	chr15:43230800-43237400	Weak transcription	Small Intestine	intestine
17	chr15:43231800-43242600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
18	chr15:43232000-43238200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
19	chr15:43232000-43362800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
20	chr15:43232400-43237400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
21	chr15:43232400-43237400	Weak transcription	Fetal Stomach	stomach
22	chr15:43232400-43243400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
23	chr15:43232600-43242200	Weak transcription	Brain Anterior Caudate	brain
24	chr15:43233800-43237400	Weak transcription	Brain Inferior Temporal Lobe	brain
25	chr15:43234000-43237200	Weak transcription	Hela-S3	cervix
26	chr15:43234000-43242200	Weak transcription	Psoas Muscle	Psoas
27	chr15:43234000-43242400	Weak transcription	K562	blood
28	chr15:43234200-43241800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
29	chr15:43234200-43242400	Weak transcription	Brain Cingulate Gyrus	brain
30	chr15:43234200-43247600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
31	chr15:43234400-43239400	Strong transcription	Left Ventricle	heart
32	chr15:43234400-43242200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
33	chr15:43234400-43242200	Weak transcription	Rectal Smooth Muscle	rectum
34	chr15:43234600-43241800	Weak transcription	Brain Angular Gyrus	brain
35	chr15:43234600-43242400	Weak transcription	NHDF-Ad	bronchial
36	chr15:43234800-43238600	Weak transcription	H1 Cell Line	embryonic stem cell
37	chr15:43234800-43239400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
38	chr15:43234800-43243400	Weak transcription	Gastric	stomach
39	chr15:43234800-43248400	Weak transcription	Pancreatic Islets	Pancreatic Islet
40	chr15:43235000-43239200	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
41	chr15:43235200-43237400	Weak transcription	Esophagus	oesophagus
42	chr15:43235200-43238600	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
43	chr15:43235200-43239400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
44	chr15:43235200-43239600	Strong transcription	Primary monocytes fromperipheralblood	blood
45	chr15:43235400-43237800	Strong transcription	NH-A	brain
46	chr15:43235400-43238200	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
47	chr15:43235400-43238400	Strong transcription	Fetal Thymus	thymus
48	chr15:43235400-43239200	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
49	chr15:43235400-43239200	Strong transcription	Primary B cells from cord blood	blood
50	chr15:43235400-43239400	Strong transcription	Primary hematopoietic stem cells	blood

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