Variant report

Variant	esv1841263
Chromosome Location	chr15:40902453-40966765
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:155)
CpG islands
(count:122)
Chromatin interactive
region (count:24)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:155 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:40916425-40916441	K562	blood:	n/a	n/a
2	ARID3A	chr15:40915575-40915775	K562	blood:	n/a	n/a
3	ARID3A	chr15:40941984-40942454	HepG2	liver:	n/a	n/a
4	BACH1	chr15:40915718-40916227	K562	blood:	n/a	n/a
5	BACH1	chr15:40917126-40917312	K562	blood:	n/a	n/a
6	BACH1	chr15:40916739-40916916	K562	blood:	n/a	n/a
7	BACH1	chr15:40914802-40915488	K562	blood:	n/a	n/a
8	BHLHE40	chr15:40964809-40965074	GM12878	blood:	n/a	n/a
9	BRCA1	chr15:40944374-40944440	Hela-S3	cervix:	n/a	n/a
10	CBX3	chr15:40957130-40957446	K562	blood:	n/a	n/a
11	CEBPB	chr15:40911280-40911283	H1-hESC	embryonic stem cell:	n/a	n/a
12	CEBPB	chr15:40917288-40917480	K562	blood:	n/a	n/a
13	CEBPB	chr15:40959213-40959500	HepG2	liver:	n/a	chr15:40959438-40959450 chr15:40959353-40959364
14	CEBPB	chr15:40917672-40917738	HepG2	liver:	n/a	chr15:40917696-40917707
15	CEBPB	chr15:40937251-40937420	HepG2	liver:	n/a	chr15:40937341-40937352
16	CTCF	chr15:40931686-40931769	GM10266	blood:	n/a	n/a
17	CTCF	chr15:40957839-40957883	LNCaP	prostate:	n/a	n/a
18	CTCF	chr15:40922776-40922812	GM13977	blood:	n/a	n/a
19	CTCF	chr15:40939040-40939190	HCT-116	colon:	n/a	n/a
20	CTCF	chr15:40909404-40909427	GM13976	blood:	n/a	n/a
21	CTCF	chr15:40916260-40916410	HCPEpiC	choroid plexus:	n/a	n/a
22	CTCF	chr15:40906623-40906694	GM20000	blood:	n/a	n/a
23	CTCF	chr15:40939040-40939190	BE2_C	brain:	n/a	n/a
24	CTCF	chr15:40903215-40903248	GM20000	blood:	n/a	n/a
25	E2F4	chr15:40934012-40934240	MCF10A-Er-Src	breast:	n/a	n/a
26	EBF1	chr15:40964665-40964959	GM12878	blood:	n/a	n/a
27	EGR1	chr15:40952844-40953121	K562	blood:	n/a	n/a
28	EP300	chr15:40953017-40953134	K562	blood:	n/a	n/a
29	EP300	chr15:40929223-40930075	SK-N-SH	brain:	n/a	n/a
30	EP300	chr15:40929665-40929894	SK-N-SH_RA	brain:	n/a	n/a
31	EP300	chr15:40929428-40929801	SK-N-SH_RA	brain:	n/a	n/a
32	FOXA1	chr15:40925452-40925704	T-47D	breast:	n/a	n/a
33	FOXA1	chr15:40933002-40933306	T-47D	breast:	n/a	n/a
34	FOXA1	chr15:40942129-40942432	HepG2	liver:	n/a	n/a
35	FOXA1	chr15:40933010-40933317	T-47D	breast:	n/a	n/a
36	FOXA1	chr15:40925436-40925786	T-47D	breast:	n/a	n/a
37	FOXA1	chr15:40942014-40942553	HepG2	liver:	n/a	n/a
38	FOXA2	chr15:40942139-40942802	HepG2	liver:	n/a	n/a
39	FOXA2	chr15:40942111-40942420	HepG2	liver:	n/a	n/a
40	GATA1	chr15:40952931-40953225	PBDE	blood:	n/a	n/a
41	GATA1	chr15:40915425-40916653	PBDE	blood:	n/a	n/a
42	GATA1	chr15:40957206-40957483	PBDE	blood:	n/a	n/a
43	GATA2	chr15:40952864-40953180	K562	blood:	n/a	n/a
44	GATA3	chr15:40933000-40933423	MCF-7	breast:	n/a	n/a
45	GATA3	chr15:40944068-40944263	SH-SY5Y	brain:	n/a	n/a
46	GATA3	chr15:40933009-40933375	T-47D	breast:	n/a	n/a
47	GATA3	chr15:40933030-40933337	T-47D	breast:	n/a	n/a
48	GATA3	chr15:40914187-40914363	SH-SY5Y	brain:	n/a	n/a
49	HEY1	chr15:40942091-40942325	HepG2	liver:	n/a	n/a
50	HEY1	chr15:40942026-40942360	HepG2	liver:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:40954471-40954521	ovcar-3	ovarian:	n/a
2	chr15:40954471-40954521	T-47D	breast:	n/a
3	chr15:40954471-40954521	BJ	skin:	n/a
4	chr15:40931170-40931220	HMEC	breast:	n/a
5	chr15:40954471-40954521	GM06990	blood:	n/a
6	chr15:40954471-40954521	GM12878	blood:	n/a
7	chr15:40931170-40931220	SK-N-SH	brain:	n/a
8	chr15:40931170-40931220	HRPEpiC	eye:	n/a
9	chr15:40931170-40931220	HRCEpiC	kidney:	n/a
10	chr15:40931170-40931220	ProgFib	skin:	n/a
11	chr15:40954471-40954521	SKMC	muscle:	n/a
12	chr15:40954471-40954521	U87	brain:	n/a
13	chr15:40954471-40954521	HCF	heart:	n/a
14	chr15:40954471-40954521	AG04449	skin:	fetal
15	chr15:40931170-40931220	CMK	blood:	n/a
16	chr15:40931170-40931220	HPAEpiC	pulmonary alveolar:	n/a
17	chr15:40954471-40954521	SK-N-SH	brain:	n/a
18	chr15:40954471-40954521	AG04450	lung:	fetal
19	chr15:40954471-40954521	HRCEpiC	kidney:	n/a
20	chr15:40954471-40954521	HepG2	liver:	n/a
21	chr15:40954471-40954521	HRPEpiC	eye:	n/a
22	chr15:40931170-40931220	NT2-D1	testis:	n/a
23	chr15:40954471-40954521	NT2-D1	testis:	n/a
24	chr15:40931170-40931220	BJ	skin:	n/a
25	chr15:40931170-40931220	Caco-2	colon:	n/a
26	chr15:40954471-40954521	SK-N-MC	brain:	n/a
27	chr15:40954471-40954521	Jurkat	blood:	n/a
28	chr15:40954471-40954521	CMK	blood:	n/a
29	chr15:40931170-40931220	H1-hESC	embryonic stem cell:	embryo
30	chr15:40954471-40954521	GM12891	blood:	n/a
31	chr15:40954471-40954521	LNCaP	prostate:	n/a
32	chr15:40954471-40954521	A549	lung:	n/a
33	chr15:40954471-40954521	MCF-7	breast:	n/a
34	chr15:40931170-40931220	HCM	heart:	n/a
35	chr15:40931170-40931220	HEEpiC	esophagus:	n/a
36	chr15:40931170-40931220	HNPCEpiC	eye:	n/a
37	chr15:40931170-40931220	GM12891	blood:	n/a
38	chr15:40931170-40931220	PANC-1	pancreas:	n/a
39	chr15:40931170-40931220	ovcar-3	ovarian:	n/a
40	chr15:40931170-40931220	HCF	heart:	n/a
41	chr15:40954471-40954521	RPTEC	kidney:	n/a
42	chr15:40954471-40954521	HEK293	kidney:	embryo
43	chr15:40931170-40931220	HUVEC	blood vessel:	n/a
44	chr15:40931170-40931220	NHBE	bronchial:	n/a
45	chr15:40954471-40954521	IMR90	lung:	fetal
46	chr15:40954471-40954521	NHDF-neo	bronchial:	n/a
47	chr15:40931170-40931220	PFSK-1	brain:	n/a
48	chr15:40931170-40931220	K562	blood:	n/a
49	chr15:40931170-40931220	Hela-S3	cervix:	n/a
50	chr15:40954471-40954521	PFSK-1	brain:	n/a

(count:24 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:40885068..40886877-chr15:40909760..40911872,2	K562	blood:
2	chr15:40907487..40910390-chr15:40913134..40917272,4	K562	blood:
3	chr15:40912062..40914734-chr15:40918334..40921407,3	K562	blood:
4	chr15:40910598..40912203-chr15:40918689..40920443,2	K562	blood:
5	chr15:40906232..40909170-chr15:40931201..40934081,2	K562	blood:
6	chr15:40906002..40908287-chr15:40919819..40922697,2	K562	blood:
7	chr15:40953000..40955816-chr15:40958237..40959774,2	K562	blood:
8	chr15:40888439..40890299-chr15:40942541..40945027,2	K562	blood:
9	chr15:40938971..40941359-chr15:40954270..40956007,2	MCF-7	breast:
10	chr15:40915820..40918459-chr15:40918962..40920817,2	K562	blood:
11	chr15:40886178..40888250-chr15:40939361..40941030,2	K562	blood:
12	chr15:40908832..40911175-chr15:40913134..40914934,3	K562	blood:
13	chr15:40906002..40908287-chr15:40919819..40922697,2	K562	blood:
14	chr15:40910551..40912670-chr15:40914146..40915843,2	K562	blood:
15	chr15:40907487..40910390-chr15:40913134..40917272,4	K562	blood:
16	chr15:40950840..40952962-chr15:40970003..40972550,2	K562	blood:
17	chr15:40904218..40906885-chr15:40912001..40913717,2	K562	blood:
18	chr15:40904218..40906885-chr15:40912001..40913717,2	K562	blood:
19	chr15:40900479..40903844-chr15:40904116..40906813,4	K562	blood:
20	chr12:1629697..1630429-chr15:40937161..40938110,2	MCF-7	breast:
21	chr15:40938971..40941359-chr15:40954270..40956007,2	MCF-7	breast:
22	chr15:40908832..40911175-chr15:40913134..40914934,3	K562	blood:
23	chr15:40900479..40903844-chr15:40904116..40906813,4	K562	blood:
24	chr15:40954350..40957294-chr15:40985826..40987543,2	K562	blood:

(count:7 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RAD51-1	chr15:40935131-40935504	ENSG00000259254.1
2	lnc-RAD51-3	chr15:40939084-40939272	NONHSAT041863
3	lnc-C15orf57-4	chr15:40907865-40908126	NONHSAT041861
4	lnc-RAD51-2	chr15:40954771-40954876	NONHSAT041864
5	lnc-RAD51-1	chr15:40938914-40939055	ENSG00000259254.1
6	lnc-RAD51-3	chr15:40942499-40942563	NONHSAT041863
7	lnc-RAD51-2	chr15:40955540-40956102	NONHSAT041864

No data

Variant related genes	Relation type
ENSG00000238559	TF binding region
ENSG00000259254	TF binding region
CASC5	TF binding region
RN7SL376P	TF binding region
ENSG00000238559	CpG island
ENSG00000259254	CpG island
CASC5	CpG island
RN7SL376P	CpG island
ENSG00000265814	chromatin interactions
ENSG00000137812	chromatin interactions
ENSG00000245849	chromatin interactions
ENSG00000051180	chromatin interactions

Extended variants
information (count: 2669 )
Associated
traits (count: 69 )

Variant overlapped rSNPs/rCNVs (count:2669 , 50 per page) page: 1 2 3 4 5 6 7 ... 54

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs16970874	chr15:40902453-40902454	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs147655679	chr15:40902458-40902459	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs576372318	chr15:40902474-40902475	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs79413475	chr15:40902490-40902491	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs200451358	chr15:40902497-40902498	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs201508618	chr15:40902499-40902500	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs376075814	chr15:40902507-40902508	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs76046797	chr15:40902567-40902568	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs572282333	chr15:40902587-40902588	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs541584751	chr15:40902624-40902625	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs560002639	chr15:40902636-40902637	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs532187422	chr15:40902646-40902647	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs373217646	chr15:40902671-40902672	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs189077163	chr15:40902676-40902677	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs28693388	chr15:40902738-40902739	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs531673680	chr15:40902839-40902840	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs548484930	chr15:40902887-40902888	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs576333130	chr15:40902915-40902916	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs148373153	chr15:40902947-40902948	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs141592887	chr15:40902973-40902974	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs533765073	chr15:40903039-40903040	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs8030491	chr15:40903051-40903052	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs570858018	chr15:40903079-40903080	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs558764843	chr15:40903099-40903100	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs539916577	chr15:40903101-40903102	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs556176834	chr15:40903226-40903227	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs576012580	chr15:40903251-40903252	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs535772914	chr15:40903296-40903297	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs10706227	chr15:40903307-40903308	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs398026961	chr15:40903320-40903321	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs79027820	chr15:40903321-40903322	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs555661758	chr15:40903327-40903328	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs572664245	chr15:40903332-40903333	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs370710915	chr15:40903349-40903350	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs541270422	chr15:40903362-40903363	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs376178803	chr15:40903369-40903370	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs368426950	chr15:40903375-40903376	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs558329035	chr15:40903388-40903389	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs576906125	chr15:40903438-40903439	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs370308962	chr15:40903455-40903456	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs138418875	chr15:40903456-40903457	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs531356404	chr15:40903504-40903505	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs541813403	chr15:40903506-40903507	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs561970267	chr15:40903526-40903527	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs530184326	chr15:40903527-40903528	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs577017270	chr15:40903544-40903545	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs142405987	chr15:40903590-40903591	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs570614047	chr15:40903595-40903596	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs533299823	chr15:40903613-40903614	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs549841349	chr15:40903617-40903618	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
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
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:645 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:40887600-40902600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
2	chr15:40887600-40941800	Weak transcription	Fetal Intestine Large	intestine
3	chr15:40887800-40933200	Weak transcription	Duodenum Mucosa	Duodenum
4	chr15:40887800-40942200	Weak transcription	Primary B cells from cord blood	blood
5	chr15:40887800-40948200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
6	chr15:40887800-40961600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
7	chr15:40888000-40903400	Weak transcription	H9 Cell Line	embryonic stem cell
8	chr15:40888000-40956000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
9	chr15:40888200-40912800	Weak transcription	HMEC	breast
10	chr15:40888400-40913200	Weak transcription	NHDF-Ad	bronchial
11	chr15:40888400-40913600	Weak transcription	NHLF	lung
12	chr15:40888400-40923200	Weak transcription	Osteobl	bone
13	chr15:40888400-40925800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
14	chr15:40888400-40944200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
15	chr15:40890800-40904800	Weak transcription	A549	lung
16	chr15:40890800-40925200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
17	chr15:40893400-40907200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr15:40893600-40922600	Weak transcription	H1 Cell Line	embryonic stem cell
19	chr15:40895000-40903200	Strong transcription	Monocytes-CD14+_RO01746	blood
20	chr15:40895800-40905200	Strong transcription	Fetal Thymus	thymus
21	chr15:40895800-40905600	Strong transcription	Dnd41	blood
22	chr15:40896000-40910200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr15:40896800-40910400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr15:40897800-40903000	Strong transcription	Primary monocytes fromperipheralblood	blood
25	chr15:40897800-40957200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr15:40898000-40902600	Strong transcription	Primary neutrophils fromperipheralblood	blood
27	chr15:40898000-40905400	Strong transcription	Primary hematopoietic stem cells short term culture	blood
28	chr15:40898200-40903200	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
29	chr15:40898200-40907800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
30	chr15:40898800-40903600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
31	chr15:40899400-40902600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
32	chr15:40899400-40922600	Weak transcription	Fetal Intestine Small	intestine
33	chr15:40899600-40911600	Weak transcription	Fetal Muscle Trunk	muscle
34	chr15:40899600-40911800	Weak transcription	Fetal Muscle Leg	muscle
35	chr15:40899600-40913200	Weak transcription	Primary hematopoietic stem cells	blood
36	chr15:40899800-40903200	Strong transcription	HUVEC	blood vessel
37	chr15:40900000-40902800	Weak transcription	GM12878-XiMat	blood
38	chr15:40900000-40943600	Weak transcription	NH-A	brain
39	chr15:40900200-40912800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
40	chr15:40900400-40913200	Weak transcription	NHEK	skin
41	chr15:40900600-40912800	Weak transcription	Muscle Satellite Cultured Cells	--
42	chr15:40901000-40902600	Strong transcription	Hela-S3	cervix
43	chr15:40901000-40902800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr15:40901000-40902800	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
45	chr15:40901200-40903000	Strong transcription	HUES48 Cell Line	embryonic stem cell
46	chr15:40901400-40905200	Strong transcription	Thymus	Thymus
47	chr15:40901600-40902800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
48	chr15:40901600-40903000	Strong transcription	K562	blood
49	chr15:40902000-40903200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
50	chr15:40902000-40903600	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell

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