Variant report

Variant	nsv984193
Chromosome Location	chr15:76214943-76221739
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr15:76220972-76221332	A549	lung:	n/a	n/a
2	CEBPB	chr15:76214159-76215031	IMR90	lung:	n/a	n/a
3	CEBPB	chr15:76214580-76215053	Hela-S3	cervix:	n/a	n/a
4	CREB1	chr15:76220968-76221342	H1-hESC	embryonic stem cell:	n/a	n/a
5	CTCF	chr15:76220996-76221938	K562	blood:	n/a	chr15:76221174-76221187
6	CTCF	chr15:76221660-76221810	A549	lung:	n/a	n/a
7	CTCF	chr15:76221100-76221250	AG09309	skin:	n/a	chr15:76221174-76221187
8	CTCF	chr15:76221680-76221830	HPAF	blood vessel:	n/a	n/a
9	CTCF	chr15:76221120-76221270	GM12868	blood:	n/a	chr15:76221174-76221187
10	CTCF	chr15:76221100-76221250	GM12871	blood:	n/a	chr15:76221174-76221187
11	CTCF	chr15:76220840-76220990	Hela-S3	cervix:	n/a	n/a
12	CTCF	chr15:76221657-76221839	LNCaP	prostate:	n/a	n/a
13	CTCF	chr15:76221080-76221230	HRPEpiC	eye:	n/a	chr15:76221174-76221187
14	CTCF	chr15:76221033-76221346	MCF-7	breast:	n/a	chr15:76221174-76221187
15	CTCF	chr15:76221680-76221830	HUVEC	blood vessel:	n/a	n/a
16	CTCF	chr15:76221040-76221190	NB4	blood:	n/a	chr15:76221174-76221187
17	CTCF	chr15:76221700-76221850	BE2_C	brain:	n/a	n/a
18	CTCF	chr15:76221100-76221250	AG10803	skin:	n/a	chr15:76221174-76221187
19	CTCF	chr15:76221080-76221230	HCT-116	colon:	n/a	chr15:76221174-76221187
20	CTCF	chr15:76220994-76221357	IMR90	lung:	n/a	chr15:76221174-76221187
21	CTCF	chr15:76221100-76221250	GM12866	blood:	n/a	chr15:76221174-76221187
22	CTCF	chr15:76221120-76221270	GM12864	blood:	n/a	chr15:76221174-76221187
23	CTCF	chr15:76221120-76221270	HRE	kidney:	n/a	chr15:76221174-76221187
24	CTCF	chr15:76221160-76221310	GM12872	blood:	n/a	chr15:76221174-76221187
25	CTCF	chr15:76221660-76221810	NB4	blood:	n/a	n/a
26	CTCF	chr15:76221041-76221291	T-47D	breast:	n/a	chr15:76221174-76221187
27	CTCF	chr15:76221093-76221277	Fibrobl	skin:	n/a	chr15:76221174-76221187
28	CTCF	chr15:76221120-76221270	HVMF	connective:	n/a	chr15:76221174-76221187
29	CTCF	chr15:76221120-76221270	MCF-7	breast:	n/a	chr15:76221174-76221187
30	CTCF	chr15:76221700-76221850	HAc	cerebellar:	n/a	n/a
31	CTCF	chr15:76221080-76221230	HPAF	blood vessel:	n/a	chr15:76221174-76221187
32	CTCF	chr15:76221064-76221271	MCF-7	breast:	n/a	chr15:76221174-76221187
33	CTCF	chr15:76221040-76221301	A549	lung:	n/a	chr15:76221174-76221187
34	CTCF	chr15:76221074-76221298	Hela-S3	cervix:	n/a	chr15:76221174-76221187
35	CTCF	chr15:76221120-76221270	HBMEC	blood vessel:	n/a	chr15:76221174-76221187
36	CTCF	chr15:76221680-76221830	GM12873	blood:	n/a	n/a
37	CTCF	chr15:76220377-76220393	Kidney_OC	kidney:	n/a	n/a
38	CTCF	chr15:76221100-76221250	GM12874	blood:	n/a	chr15:76221174-76221187
39	CTCF	chr15:76221080-76221230	HCM	heart:	n/a	chr15:76221174-76221187
40	CTCF	chr15:76221028-76221366	K562	blood:	n/a	chr15:76221174-76221187
41	CTCF	chr15:76221068-76221224	SK-N-SH_RA	brain:	n/a	chr15:76221174-76221187
42	CTCF	chr15:76221720-76221870	GM12864	blood:	n/a	n/a
43	CTCF	chr15:76221160-76221310	GM12871	blood:	n/a	chr15:76221174-76221187
44	CTCF	chr15:76221680-76221830	AG04450	lung:	n/a	n/a
45	CTCF	chr15:76221100-76221250	HPF	lung:	n/a	chr15:76221174-76221187
46	CTCF	chr15:76221120-76221270	NHEK	skin:	n/a	chr15:76221174-76221187
47	CTCF	chr15:76221710-76221810	HepG2	liver:	n/a	n/a
48	CTCF	chr15:76221680-76221830	GM06990	blood:	n/a	n/a
49	CTCF	chr15:76221100-76221250	AG09319	gingival:	n/a	chr15:76221174-76221187
50	CTCF	chr15:76221120-76221270	AoAF	blood vessel:	n/a	chr15:76221174-76221187

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:76218542-76218592	NH-A	brain:	n/a
2	chr15:76218542-76218592	HMEC	breast:	n/a
3	chr15:76218542-76218592	HAEpiC	amniotic membrane:	n/a
4	chr15:76218542-76218592	CMK	blood:	n/a
5	chr15:76218542-76218592	SAEC	small airway:	n/a
6	chr15:76218542-76218592	AG04450	lung:	fetal
7	chr15:76218542-76218592	AoSMC	blood vessel:	n/a
8	chr15:76218542-76218592	Hepatocyte	liver:	n/a
9	chr15:76218542-76218592	AG04449	skin:	fetal
10	chr15:76218542-76218592	ovcar-3	ovarian:	n/a
11	chr15:76218542-76218592	GM12892	blood:	n/a
12	chr15:76218542-76218592	NB4	blood:	n/a
13	chr15:76218542-76218592	HEK293	kidney:	embryo
14	chr15:76218542-76218592	Caco-2	colon:	n/a
15	chr15:76218542-76218592	HUVEC	blood vessel:	n/a
16	chr15:76218542-76218592	SK-N-MC	brain:	n/a
17	chr15:76218542-76218592	HNPCEpiC	eye:	n/a
18	chr15:76218542-76218592	GM12891	blood:	n/a
19	chr15:76218542-76218592	SK-N-SH	brain:	n/a
20	chr15:76218542-76218592	GM19239	blood:	n/a
21	chr15:76218542-76218592	RPTEC	kidney:	n/a
22	chr15:76218542-76218592	PANC-1	pancreas:	n/a
23	chr15:76218542-76218592	GM06990	blood:	n/a
24	chr15:76218542-76218592	ProgFib	skin:	n/a
25	chr15:76218542-76218592	MCF10A-Er-Src	breast:	n/a
26	chr15:76218542-76218592	AG09309	skin:	n/a
27	chr15:76218542-76218592	AG10803	skin:	n/a
28	chr15:76218542-76218592	SK-N-SH_RA	brain:	n/a
29	chr15:76218542-76218592	HIPEpiC	eye:	n/a
30	chr15:76218542-76218592	MCF-7	breast:	n/a
31	chr15:76218542-76218592	IMR90	lung:	fetal
32	chr15:76218542-76218592	AG09319	gingival:	n/a
33	chr15:76218542-76218592	HepG2	liver:	n/a
34	chr15:76218542-76218592	HEEpiC	esophagus:	n/a
35	chr15:76218542-76218592	K562	blood:	n/a
36	chr15:76218542-76218592	HCM	heart:	n/a
37	chr15:76218542-76218592	U87	brain:	n/a
38	chr15:76218542-76218592	HCPEpiC	choroid plexus:	n/a
39	chr15:76218542-76218592	SKMC	muscle:	n/a
40	chr15:76218542-76218592	HRE	kidney:	n/a
41	chr15:76218542-76218592	A549	lung:	n/a
42	chr15:76218542-76218592	HRCEpiC	kidney:	n/a
43	chr15:76218542-76218592	PFSK-1	brain:	n/a
44	chr15:76218542-76218592	HCF	heart:	n/a
45	chr15:76218542-76218592	HCT-116	colon:	n/a
46	chr15:76218542-76218592	Hela-S3	cervix:	n/a
47	chr15:76218542-76218592	ECC-1	luminal epithelium:	n/a
48	chr15:76218542-76218592	HRPEpiC	eye:	n/a
49	chr15:76218542-76218592	T-47D	breast:	n/a
50	chr15:76218542-76218592	HPAEpiC	pulmonary alveolar:	n/a

No.	Distal block	Cell Line	Cell type
1	chr15:76218432..76221221-chr15:76222501..76224322,2	K562	blood:
2	chr15:76211169..76212903-chr15:76216124..76218574,2	K562	blood:
3	chr15:76100272..76101901-chr15:76213487..76215015,2	MCF-7	breast:
4	chr15:76220909..76222483-chr15:76431367..76432547,6	MCF-7	breast:
5	chr15:76134738..76137531-chr15:76213664..76217396,4	MCF-7	breast:
6	chr15:76102027..76103101-chr15:76220766..76221842,9	MCF-7	breast:
7	chr15:76221299..76222193-chr15:76443491..76444002,2	MCF-7	breast:

Variant related genes	Relation type
FBXO22	TF binding region
FBXO22	CpG island
ENSG00000140367	chromatin interactions

Extended variants
information (count: 212 )
Associated
traits (count: 54 )

Variant overlapped rSNPs/rCNVs (count:212 , 50 per page) page: 1 2 3 4 5

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs190619210	chr15:76215031-76215032	Strong transcription Weak transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs145961451	chr15:76215043-76215044	Strong transcription Weak transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs373916662	chr15:76215074-76215075	Strong transcription Weak transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs182263467	chr15:76215081-76215082	Strong transcription Weak transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs548160883	chr15:76215112-76215113	Strong transcription Weak transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs537945620	chr15:76215194-76215195	Strong transcription Weak transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs78653469	chr15:76215220-76215221	Strong transcription Weak transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs536784247	chr15:76215260-76215261	Strong transcription Weak transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs185200420	chr15:76215319-76215320	Strong transcription Weak transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs570579207	chr15:76215380-76215381	Strong transcription Weak transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs534484070	chr15:76215396-76215397	Strong transcription Weak transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs200990698	chr15:76215409-76215410	Strong transcription Weak transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs78060086	chr15:76215467-76215468	Strong transcription Weak transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs574352228	chr15:76215607-76215608	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs139868423	chr15:76215614-76215615	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs554714335	chr15:76215643-76215644	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs576377655	chr15:76215676-76215677	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs543588223	chr15:76215715-76215716	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs189879768	chr15:76215763-76215764	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs371508950	chr15:76215796-76215797	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs181590779	chr15:76215823-76215824	Genic enhancers Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs541597972	chr15:76215964-76215965	Genic enhancers Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs551151324	chr15:76215987-76215988	Genic enhancers Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs571312735	chr15:76215999-76216000	Genic enhancers Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs560091105	chr15:76216077-76216078	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs530464240	chr15:76216130-76216131	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs55782145	chr15:76216154-76216155	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
28	rs569583015	chr15:76216238-76216239	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs553515017	chr15:76216256-76216257	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs377274979	chr15:76216312-76216313	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs185318903	chr15:76216320-76216321	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs552005687	chr15:76216335-76216336	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs55828994	chr15:76216342-76216343	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
34	rs560204888	chr15:76216353-76216354	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs534521595	chr15:76216374-76216375	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs1617498	chr15:76216382-76216383	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs35865885	chr15:76216437-76216438	Weak transcription Genic enhancers Strong transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs36061952	chr15:76216452-76216453	Weak transcription Genic enhancers Strong transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs10152926	chr15:76216455-76216456	Weak transcription Genic enhancers Strong transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs372421282	chr15:76216555-76216556	Weak transcription Genic enhancers Strong transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs60191258	chr15:76216626-76216627	Enhancers Weak transcription Genic enhancers Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
42	rs190128043	chr15:76216640-76216641	Enhancers Weak transcription Genic enhancers Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs575195636	chr15:76216873-76216874	Weak transcription Enhancers Genic enhancers Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs576388301	chr15:76216874-76216875	Weak transcription Enhancers Genic enhancers Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs544583079	chr15:76216890-76216891	Weak transcription Enhancers Genic enhancers Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs543764410	chr15:76216958-76216959	Weak transcription Enhancers Genic enhancers Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs76586437	chr15:76216986-76216987	Weak transcription Enhancers Genic enhancers Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs551172658	chr15:76217012-76217013	Enhancers Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs369526303	chr15:76217036-76217037	Enhancers Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs561372478	chr15:76217050-76217051	Enhancers Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:54)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	CNVD
Wilms tumour	21544195	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
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
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Multiple myeloma	20724749	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Cancer	16751803	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Breast cancer	17133270	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	17322880	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Lung cancer	18438408	CNVD
Multiple myeloma	16616336	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Papillary thyroid carcinoma	22161024	CNVD
Autism	21480499	CNVD
Breast cancer	17603634	CNVD
Acute myeloid leukemia	16864856	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:409 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:76197200-76216800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr15:76197200-76216800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr15:76197800-76217400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
4	chr15:76198000-76231600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr15:76198200-76232200	Weak transcription	Pancreatic Islets	Pancreatic Islet
6	chr15:76198400-76225000	Weak transcription	Fetal Kidney	kidney
7	chr15:76198600-76217000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
8	chr15:76198600-76226400	Weak transcription	Fetal Brain Male	brain
9	chr15:76199000-76215800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
10	chr15:76203800-76230200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr15:76205400-76215400	Strong transcription	iPS-18 Cell Line	embryonic stem cell
12	chr15:76205400-76217200	Strong transcription	HUES48 Cell Line	embryonic stem cell
13	chr15:76205400-76217200	Strong transcription	Monocytes-CD14+_RO01746	blood
14	chr15:76205400-76218600	Strong transcription	iPS-20b Cell Line	embryonic stem cell
15	chr15:76205600-76216200	Strong transcription	HUES6 Cell Line	embryonic stem cell
16	chr15:76205600-76216400	Strong transcription	H1 Cell Line	embryonic stem cell
17	chr15:76205800-76216800	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr15:76206800-76218800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
19	chr15:76207000-76226600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
20	chr15:76207000-76228200	Weak transcription	Brain Substantia Nigra	brain
21	chr15:76207000-76228200	Weak transcription	Colonic Mucosa	Colon
22	chr15:76207000-76232000	Weak transcription	Rectal Smooth Muscle	rectum
23	chr15:76207200-76225000	Weak transcription	Spleen	Spleen
24	chr15:76207200-76226600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
25	chr15:76207400-76216800	Weak transcription	Placenta Amnion	Placenta Amnion
26	chr15:76207400-76218000	Weak transcription	Brain Germinal Matrix	brain
27	chr15:76207400-76222200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
28	chr15:76207400-76222200	Weak transcription	Brain Angular Gyrus	brain
29	chr15:76207400-76223000	Weak transcription	Brain Cingulate Gyrus	brain
30	chr15:76208000-76222400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
31	chr15:76208400-76232800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
32	chr15:76209000-76216600	Weak transcription	Fetal Brain Female	brain
33	chr15:76209000-76225000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr15:76209000-76225000	Weak transcription	Stomach Smooth Muscle	stomach
35	chr15:76209600-76217200	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
36	chr15:76209600-76219600	Strong transcription	K562	blood
37	chr15:76209800-76222800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
38	chr15:76210200-76215600	Strong transcription	GM12878-XiMat	blood
39	chr15:76210200-76222200	Strong transcription	Primary T cells from cord blood	blood
40	chr15:76210800-76225000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
41	chr15:76211400-76215600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
42	chr15:76211400-76240200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
43	chr15:76212000-76216400	Strong transcription	Dnd41	blood
44	chr15:76212000-76218200	Genic enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
45	chr15:76212200-76217800	Weak transcription	Primary neutrophils fromperipheralblood	blood
46	chr15:76212200-76222600	Weak transcription	Cortex derived primary cultured neurospheres	brain
47	chr15:76212400-76216800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
48	chr15:76212400-76223400	Strong transcription	HepG2	liver
49	chr15:76212600-76215800	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
50	chr15:76212600-76216200	Weak transcription	Aorta	Aorta

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