Variant report

Variant	esv3335467
Chromosome Location	chr15:40213096-40213565
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	ATF2	chr15:40212646-40213505	H1-hESC	embryonic stem cell:	n/a	n/a
2	ATF3	chr15:40213019-40213368	H1-hESC	embryonic stem cell:	n/a	chr15:40213153-40213162 chr15:40213175-40213195
3	ATF3	chr15:40212987-40213349	K562	blood:	n/a	chr15:40213153-40213162 chr15:40213175-40213195
4	ATF3	chr15:40213055-40213300	HepG2	liver:	n/a	chr15:40213153-40213162 chr15:40213175-40213195
5	BACH1	chr15:40212357-40213516	H1-hESC	embryonic stem cell:	n/a	n/a
6	BHLHE40	chr15:40213016-40213416	HepG2	liver:	n/a	chr15:40213173-40213186 chr15:40213205-40213221 chr15:40213143-40213159 chr15:40213213-40213229
7	BHLHE40	chr15:40212964-40213444	K562	blood:	n/a	chr15:40213173-40213186 chr15:40213205-40213221 chr15:40213143-40213159 chr15:40213213-40213229
8	BHLHE40	chr15:40212974-40213463	GM12878	blood:	n/a	chr15:40213173-40213186 chr15:40213205-40213221 chr15:40213143-40213159 chr15:40213213-40213229
9	CBX3	chr15:40213156-40213541	K562	blood:	n/a	n/a
10	CBX3	chr15:40212976-40213501	K562	blood:	n/a	n/a
11	CCNT2	chr15:40212951-40213473	K562	blood:	n/a	chr15:40213193-40213202
12	CHD1	chr15:40212898-40213494	GM12878	blood:	n/a	chr15:40213198-40213208 chr15:40212983-40212990
13	CHD1	chr15:40210279-40213585	H1-hESC	embryonic stem cell:	n/a	chr15:40213198-40213208 chr15:40212983-40212990
14	CHD2	chr15:40212980-40213446	Hela-S3	cervix:	n/a	chr15:40213198-40213208 chr15:40212983-40212990
15	CHD2	chr15:40213069-40213400	GM12878	blood:	n/a	chr15:40213198-40213208
16	CHD2	chr15:40212902-40213124	H1-hESC	embryonic stem cell:	n/a	chr15:40212983-40212990
17	CHD2	chr15:40213252-40213412	K562	blood:	n/a	n/a
18	CREB1	chr15:40212888-40213352	A549	lung:	n/a	chr15:40213173-40213186
19	CTBP2	chr15:40211745-40213391	H1-hESC	embryonic stem cell:	n/a	n/a
20	CTCF	chr15:40213000-40213150	HMEC	breast:	n/a	n/a
21	CTCF	chr15:40213000-40213150	AoAF	blood vessel:	n/a	n/a
22	CTCF	chr15:40213076-40213132	MCF-7	breast:	n/a	n/a
23	CTCF	chr15:40212980-40213130	HepG2	liver:	n/a	n/a
24	CTCF	chr15:40213046-40213126	Pancreas_OC	pancreas:	n/a	n/a
25	CTCF	chr15:40213004-40213205	GM10266	blood:	n/a	chr15:40213145-40213158
26	CTCF	chr15:40212980-40213130	HRE	kidney:	n/a	n/a
27	CTCF	chr15:40212980-40213130	GM12875	blood:	n/a	n/a
28	CTCF	chr15:40213040-40213296	MCF-7	breast:	n/a	chr15:40213145-40213158
29	CTCF	chr15:40213220-40213370	GM12874	blood:	n/a	n/a
30	CTCF	chr15:40213000-40213150	GM12865	blood:	n/a	n/a
31	CTCF	chr15:40212867-40213324	K562	blood:	n/a	chr15:40213145-40213158
32	CTCF	chr15:40213060-40213210	GM12873	blood:	n/a	chr15:40213145-40213158
33	CTCF	chr15:40212980-40213130	HPAF	blood vessel:	n/a	n/a
34	CTCF	chr15:40213040-40213190	HFF	foreskin:	n/a	chr15:40213145-40213158
35	CTCF	chr15:40213020-40213170	GM12866	blood:	n/a	chr15:40213145-40213158
36	CTCF	chr15:40213072-40213272	A549	lung:	n/a	chr15:40213145-40213158
37	CTCF	chr15:40212404-40213226	IMR90	lung:	n/a	chr15:40212458-40212476 chr15:40213145-40213158 chr15:40212461-40212474 chr15:40212460-40212481
38	CTCF	chr15:40213102-40213315	GM12892	blood:	n/a	chr15:40213145-40213158
39	CTCF	chr15:40212960-40213110	HBMEC	blood vessel:	n/a	n/a
40	CTCF	chr15:40213160-40213310	SAEC	small airway:	n/a	n/a
41	CTCF	chr15:40213024-40213230	SK-N-SH_RA	brain:	n/a	chr15:40213145-40213158
42	CTCF	chr15:40213013-40213148	GM10248	blood:	n/a	n/a
43	CTCF	chr15:40212960-40213110	SAEC	small airway:	n/a	n/a
44	CTCF	chr15:40213080-40213230	GM12866	blood:	n/a	chr15:40213145-40213158
45	CTCF	chr15:40213031-40213171	H1-hESC	embryonic stem cell:	n/a	chr15:40213145-40213158
46	CTCF	chr15:40212960-40213110	AG04450	lung:	n/a	n/a
47	CTCF	chr15:40212937-40213400	GM12878	blood:	n/a	chr15:40213145-40213158
48	CTCF	chr15:40213066-40213180	Hela-S3	cervix:	n/a	chr15:40213145-40213158
49	CTCF	chr15:40212860-40213210	GM06990	blood:	n/a	chr15:40213145-40213158
50	CTCF	chr15:40213088-40213127	GM12878	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:40213409-40213459	HMEC	breast:	n/a
2	chr15:40213270-40213320	HRPEpiC	eye:	n/a
3	chr15:40213339-40213389	Jurkat	blood:	n/a
4	chr15:40213339-40213389	IMR90	lung:	fetal
5	chr15:40213326-40213376	SAEC	small airway:	n/a
6	chr15:40213280-40213330	SK-N-SH	brain:	n/a
7	chr15:40213409-40213459	NH-A	brain:	n/a
8	chr15:40213280-40213330	HRE	kidney:	n/a
9	chr15:40213326-40213376	PANC-1	pancreas:	n/a
10	chr15:40213326-40213376	HCM	heart:	n/a
11	chr15:40213280-40213330	NH-A	brain:	n/a
12	chr15:40213280-40213330	Jurkat	blood:	n/a
13	chr15:40213409-40213459	AG10803	skin:	n/a
14	chr15:40213409-40213459	HRCEpiC	kidney:	n/a
15	chr15:40213270-40213320	Hela-S3	cervix:	n/a
16	chr15:40213314-40213364	AG09309	skin:	n/a
17	chr15:40213339-40213389	HUVEC	blood vessel:	n/a
18	chr15:40213270-40213320	SK-N-SH	brain:	n/a
19	chr15:40213280-40213330	BJ	skin:	n/a
20	chr15:40213339-40213389	NHBE	bronchial:	n/a
21	chr15:40213339-40213389	RPTEC	kidney:	n/a
22	chr15:40213339-40213389	HepG2	liver:	n/a
23	chr15:40213339-40213389	HIPEpiC	eye:	n/a
24	chr15:40213409-40213459	AG04449	skin:	fetal
25	chr15:40213326-40213376	HCF	heart:	n/a
26	chr15:40213409-40213459	PANC-1	pancreas:	n/a
27	chr15:40213409-40213459	GM19239	blood:	n/a
28	chr15:40213270-40213320	RPTEC	kidney:	n/a
29	chr15:40213280-40213330	HCT-116	colon:	n/a
30	chr15:40213326-40213376	HCPEpiC	choroid plexus:	n/a
31	chr15:40213339-40213389	GM19239	blood:	n/a
32	chr15:40213280-40213330	AG09309	skin:	n/a
33	chr15:40213339-40213389	NHDF-neo	bronchial:	n/a
34	chr15:40213270-40213320	NT2-D1	testis:	n/a
35	chr15:40213339-40213389	Hela-S3	cervix:	n/a
36	chr15:40213280-40213330	PANC-1	pancreas:	n/a
37	chr15:40213339-40213389	HNPCEpiC	eye:	n/a
38	chr15:40213326-40213376	Hepatocyte	liver:	n/a
39	chr15:40213339-40213389	HEK293	kidney:	embryo
40	chr15:40213409-40213459	RPTEC	kidney:	n/a
41	chr15:40213339-40213389	CMK	blood:	n/a
42	chr15:40213280-40213330	CMK	blood:	n/a
43	chr15:40213314-40213364	HRE	kidney:	n/a
44	chr15:40213314-40213364	HepG2	liver:	n/a
45	chr15:40213409-40213459	HPAEpiC	pulmonary alveolar:	n/a
46	chr15:40213270-40213320	HepG2	liver:	n/a
47	chr15:40213409-40213459	HL-60	blood:	n/a
48	chr15:40213270-40213320	A549	lung:	n/a
49	chr15:40213339-40213389	HAEpiC	amniotic membrane:	n/a
50	chr15:40213314-40213364	GM12891	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr15:40213124..40213699-chr17:67323085..67323765,2	Hela-S3	cervix:
2	chr15:40211846..40214390-chr15:40224576..40226655,2	K562	blood:
3	chr15:40211366..40214080-chr15:40223428..40228644,6	MCF-7	breast:
4	chr1:204042666..204043286-chr15:40213090..40213711,2	Hela-S3	cervix:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-EIF2AK4-1	chr15:40213228-40213887	XLOC_011218
2	lnc-EIF2AK4-1	chr15:40213271-40218081	ENSG00000246863.2
3	lnc-EIF2AK4-1	chr15:40213228-40213743	XLOC_011218
4	lnc-EIF2AK4-1	chr15:40213243-40213859	ENSG00000246863
5	lnc-EIF2AK4-1	chr15:40213243-40213859	ENSG00000246863.2
6	lnc-EIF2AK4-1	chr15:40213228-40213748	XLOC_011218

Variant related genes	Relation type
ENSG00000246863	TF binding region
GPR176	TF binding region
ENSG00000246863	CpG island
GPR176	CpG island
ENSG00000143842	chromatin interactions
ENSG00000154265	chromatin interactions
ENSG00000128829	chromatin interactions
MYBL1	miRNA target sites
ERBB4	miRNA target sites

Extended variants
information (count: 25 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:25 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs571395116	chr15:40213141-40213142	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
2	rs369978615	chr15:40213149-40213150	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
3	rs536992480	chr15:40213184-40213185	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
4	rs550460925	chr15:40213186-40213187	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
5	rs2917497	chr15:40213192-40213193	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
6	rs536256897	chr15:40213198-40213199	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
7	rs553298496	chr15:40213211-40213212	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
8	rs143147653	chr15:40213215-40213216	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
9	rs539101736	chr15:40213226-40213227	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
10	rs558919626	chr15:40213238-40213239	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
11	rs575783716	chr15:40213250-40213251	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
12	rs544966353	chr15:40213254-40213255	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
13	rs561569174	chr15:40213269-40213270	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
14	rs370323484	chr15:40213322-40213323	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
15	rs542657534	chr15:40213328-40213329	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
16	rs559270597	chr15:40213350-40213351	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
17	rs528199981	chr15:40213356-40213357	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
18	rs373600799	chr15:40213384-40213385	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
19	rs114202341	chr15:40213411-40213412	Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
20	rs530624848	chr15:40213430-40213431	Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
21	rs550321572	chr15:40213432-40213433	Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
22	rs567240514	chr15:40213436-40213437	Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
23	rs568128779	chr15:40213450-40213451	Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
24	rs529911495	chr15:40213465-40213466	Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
25	rs3759837	chr15:40213508-40213509	Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region lncRNA	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	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
Myelofibrosis	22110671	CNVD
Cancer	21129771	CNVD
Breast cancer	21045282	CNVD
Papillary thyroid carcinoma	22161024	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	22032731	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Ovarian cancer	21720365	CNVD
Multiple myeloma	16616336	CNVD
Renal cell carcinoma	18765545	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD

Chromatin state (count:180 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:40209200-40213400	Active TSS	HUES48 Cell Line	embryonic stem cell
2	chr15:40209200-40213800	Active TSS	iPS-15b Cell Line	embryonic stem cell
3	chr15:40209800-40213800	Active TSS	H1 Cell Line	embryonic stem cell
4	chr15:40210000-40213600	Active TSS	H9 Cell Line	embryonic stem cell
5	chr15:40210200-40213600	Active TSS	ES-WA7 Cell Line	embryonic stem cell
6	chr15:40210200-40213600	Active TSS	NHLF	lung
7	chr15:40210400-40213400	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
8	chr15:40210400-40213400	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
9	chr15:40210400-40213600	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
10	chr15:40210400-40213600	Active TSS	Aorta	Aorta
11	chr15:40210400-40213800	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
12	chr15:40210600-40213800	Active TSS	HSMM	muscle
13	chr15:40210800-40213400	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
14	chr15:40210800-40213400	Active TSS	HSMMtube	muscle
15	chr15:40210800-40213600	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr15:40210800-40213600	Active TSS	NHDF-Ad	bronchial
17	chr15:40210800-40213800	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
18	chr15:40211000-40213400	Active TSS	Osteobl	bone
19	chr15:40211000-40213600	Bivalent/Poised TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
20	chr15:40211000-40213600	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr15:40211000-40213600	Active TSS	Brain Anterior Caudate	brain
22	chr15:40211200-40213600	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
23	chr15:40211200-40213600	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
24	chr15:40211200-40213800	Active TSS	Brain Angular Gyrus	brain
25	chr15:40211200-40213800	Active TSS	Pancreatic Islets	Pancreatic Islet
26	chr15:40211400-40213400	Active TSS	NHEK	skin
27	chr15:40211600-40213400	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
28	chr15:40211600-40213400	Active TSS	Hela-S3	cervix
29	chr15:40211600-40213600	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr15:40211600-40213800	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
31	chr15:40211800-40213200	Flanking Active TSS	Liver	Liver
32	chr15:40211800-40213200	Flanking Bivalent TSS/Enh	Colonic Mucosa	Colon
33	chr15:40211800-40213200	Flanking Active TSS	Pancreas	Pancrea
34	chr15:40211800-40213600	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
35	chr15:40211800-40213600	Flanking Bivalent TSS/Enh	Primary neutrophils fromperipheralblood	blood
36	chr15:40211800-40213600	Flanking Bivalent TSS/Enh	Primary T cells fromperipheralblood	blood
37	chr15:40211800-40213800	Flanking Bivalent TSS/Enh	Primary monocytes fromperipheralblood	blood
38	chr15:40211800-40213800	Flanking Active TSS	Primary hematopoietic stem cells	blood
39	chr15:40211800-40213800	Flanking Bivalent TSS/Enh	Monocytes-CD14+_RO01746	blood
40	chr15:40212000-40213400	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
41	chr15:40212000-40213800	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
42	chr15:40212200-40213200	Flanking Active TSS	Stomach Smooth Muscle	stomach
43	chr15:40212200-40213800	Active TSS	Colon Smooth Muscle	Colon
44	chr15:40212400-40213400	Bivalent/Poised TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr15:40212400-40213400	Bivalent/Poised TSS	H9 Derived Neuron Cultured Cells	ES cell derived
46	chr15:40212400-40213600	Flanking Bivalent TSS/Enh	Primary Natural Killer cells fromperipheralblood	blood
47	chr15:40212400-40213600	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
48	chr15:40212400-40213800	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
49	chr15:40212600-40213400	Active TSS	HUES64 Cell Line	embryonic stem cell
50	chr15:40212600-40213600	Active TSS	ES-I3 Cell Line	embryonic stem cell

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