Variant report

Variant	rs111525339
Chromosome Location	chr14:105766991-105766992
allele	C/G
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	CREB1	chr14:105766729-105768188	A549	lung:	n/a	n/a
2	BHLHE40	chr14:105766686-105767711	HepG2	liver:	n/a	chr14:105766760-105766776
3	SIN3A	chr14:105766506-105768237	H1-hESC	embryonic stem cell:	n/a	chr14:105766977-105766990 chr14:105768126-105768134 chr14:105766760-105766769 chr14:105768124-105768133 chr14:105766984-105766993 chr14:105767859-105767872 chr14:105767853-105767866 chr14:105767702-105767715
4	YY1	chr14:105766760-105768104	HepG2	liver:	n/a	chr14:105767659-105767668 chr14:105766983-105766997 chr14:105766970-105766984 chr14:105766982-105766996
5	YY1	chr14:105766863-105767068	K562	blood:	n/a	chr14:105766983-105766997 chr14:105766970-105766984 chr14:105766982-105766996
6	MAX	chr14:105766987-105767144	K562	blood:	n/a	n/a
7	POLR2A	chr14:105766819-105768162	HepG2	liver:	n/a	n/a
8	CHD2	chr14:105766846-105767883	GM12878	blood:	n/a	n/a
9	MYC	chr14:105766770-105768069	NB4	blood:	n/a	chr14:105767652-105767662 chr14:105767916-105767926 chr14:105767844-105767854 chr14:105767708-105767718 chr14:105767751-105767761 chr14:105767785-105767795
10	POLR2A	chr14:105766770-105767815	GM19193	blood:	n/a	n/a
11	PAX5	chr14:105766542-105767569	GM12892	blood:	n/a	n/a
12	SIN3AK20	chr14:105766843-105767744	PANC-1	pancreas:	n/a	n/a
13	BRCA1	chr14:105766843-105767916	Hela-S3	cervix:	n/a	n/a
14	CHD2	chr14:105766863-105767699	HepG2	liver:	n/a	n/a
15	HCFC1	chr14:105765946-105768196	Hela-S3	cervix:	n/a	n/a
16	POLR2A	chr14:105766794-105767998	GM19099	blood:	n/a	n/a
17	HEY1	chr14:105766813-105767414	HepG2	liver:	n/a	chr14:105766968-105766983
18	POLR2A	chr14:105766711-105767698	A549	lung:	n/a	n/a
19	JUND	chr14:105766780-105767978	A549	lung:	n/a	chr14:105767658-105767667
20	POLR2A	chr14:105766762-105768115	MCF10A-Er-Src	breast:	n/a	n/a
21	POLR2A	chr14:105766664-105767733	A549	lung:	n/a	n/a
22	TCF12	chr14:105766782-105767116	GM12878	blood:	n/a	n/a
23	RCOR1	chr14:105766667-105768078	GM12878	blood:	n/a	n/a
24	POLR2A	chr14:105766761-105767969	GM18951	blood:	n/a	n/a
25	MAX	chr14:105766517-105767295	ECC-1	luminal epithelium:	n/a	chr14:105766553-105766562
26	POLR2A	chr14:105766759-105767797	IMR90	lung:	n/a	n/a
27	POLR2A	chr14:105766689-105767693	PBDE	blood:	n/a	n/a
28	E2F6	chr14:105766700-105767644	K562	blood:	n/a	n/a
29	MAX	chr14:105766634-105767867	SK-N-SH	brain:	n/a	chr14:105767652-105767662 chr14:105767844-105767854 chr14:105767708-105767718 chr14:105767751-105767761 chr14:105767785-105767795
30	HMGN3	chr14:105766757-105768119	K562	blood:	n/a	n/a
31	POLR2A	chr14:105766720-105767850	GM12878	blood:	n/a	n/a
32	MTA3	chr14:105765789-105767734	GM12878	blood:	n/a	n/a
33	POLR2A	chr14:105766543-105767764	GM12878	blood:	n/a	n/a
34	POLR2A	chr14:105766865-105768162	HCT-116	colon:	n/a	n/a
35	MXI1	chr14:105766108-105768085	GM12878	blood:	n/a	n/a
36	POLR2A	chr14:105766753-105768219	HUVEC	blood vessel:	n/a	n/a
37	POLR2A	chr14:105766650-105768012	Hela-S3	cervix:	n/a	n/a
38	POLR2A	chr14:105766625-105768562	K562	blood:	n/a	n/a
39	HCFC1	chr14:105766865-105767913	K562	blood:	n/a	n/a
40	SIN3AK20	chr14:105766848-105767579	SK-N-SH	brain:	n/a	n/a
41	ZNF263	chr14:105766620-105767721	HEK293-T-REx	kidney:	n/a	n/a
42	BCLAF1	chr14:105766850-105767395	GM12878	blood:	n/a	n/a
43	POLR2A	chr14:105766694-105767734	HUVEC	blood vessel:	n/a	n/a
44	MYC	chr14:105766600-105768177	K562	blood:	n/a	chr14:105767652-105767662 chr14:105767916-105767926 chr14:105767844-105767854 chr14:105767708-105767718 chr14:105767751-105767761 chr14:105767785-105767795
45	CCNT2	chr14:105766686-105768120	K562	blood:	n/a	chr14:105767659-105767668
46	POLR2A	chr14:105766818-105767791	GM18526	blood:	n/a	n/a
47	ZBTB33	chr14:105766984-105767291	HepG2	liver:	n/a	chr14:105767075-105767090
48	EBF1	chr14:105766868-105767294	GM12878	blood:	n/a	n/a
49	POLR2A	chr14:105766569-105767782	GM12892	blood:	n/a	n/a
50	MYC	chr14:105766796-105766993	MCF-7	breast:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:105766991-105767041	HIPEpiC	eye:	n/a
2	chr14:105766991-105767041	AG04449	skin:	fetal
3	chr14:105766987-105767037	GM06990	blood:	n/a
4	chr14:105766987-105767037	HEEpiC	esophagus:	n/a
5	chr14:105766987-105767037	Hepatocyte	liver:	n/a
6	chr14:105766987-105767037	AG04449	skin:	fetal
7	chr14:105766991-105767041	BJ	skin:	n/a
8	chr14:105766991-105767041	SK-N-SH	brain:	n/a
9	chr14:105766991-105767041	AG09309	skin:	n/a
10	chr14:105766987-105767037	NHBE	bronchial:	n/a
11	chr14:105766987-105767037	GM12891	blood:	n/a
12	chr14:105766987-105767037	Hela-S3	cervix:	n/a
13	chr14:105766987-105767037	HAEpiC	amniotic membrane:	n/a
14	chr14:105766991-105767041	Caco-2	colon:	n/a
15	chr14:105766987-105767037	GM12878	blood:	n/a
16	chr14:105766987-105767037	SK-N-MC	brain:	n/a
17	chr14:105766987-105767037	AG10803	skin:	n/a
18	chr14:105766987-105767037	Caco-2	colon:	n/a
19	chr14:105766991-105767041	ProgFib	skin:	n/a
20	chr14:105766987-105767037	HNPCEpiC	eye:	n/a
21	chr14:105766991-105767041	HEEpiC	esophagus:	n/a
22	chr14:105766991-105767041	MCF-7	breast:	n/a
23	chr14:105766987-105767037	MCF10A-Er-Src	breast:	n/a
24	chr14:105766991-105767041	NHDF-neo	bronchial:	n/a
25	chr14:105766987-105767037	HIPEpiC	eye:	n/a
26	chr14:105766987-105767037	NHDF-neo	bronchial:	n/a
27	chr14:105766987-105767037	HCF	heart:	n/a
28	chr14:105766991-105767041	IMR90	lung:	fetal
29	chr14:105766987-105767037	HRE	kidney:	n/a
30	chr14:105766991-105767041	AG04450	lung:	fetal
31	chr14:105766991-105767041	HRE	kidney:	n/a
32	chr14:105766987-105767037	ProgFib	skin:	n/a
33	chr14:105766991-105767041	HPAEpiC	pulmonary alveolar:	n/a
34	chr14:105766991-105767041	NT2-D1	testis:	n/a
35	chr14:105766987-105767037	PFSK-1	brain:	n/a
36	chr14:105766991-105767041	AoSMC	blood vessel:	n/a
37	chr14:105766987-105767037	HRPEpiC	eye:	n/a
38	chr14:105766991-105767041	HEK293	kidney:	embryo
39	chr14:105766991-105767041	HCM	heart:	n/a
40	chr14:105766991-105767041	GM19239	blood:	n/a
41	chr14:105766987-105767037	Jurkat	blood:	n/a
42	chr14:105766987-105767037	AG09309	skin:	n/a
43	chr14:105766991-105767041	NHBE	bronchial:	n/a
44	chr14:105766991-105767041	Hela-S3	cervix:	n/a
45	chr14:105766991-105767041	HUVEC	blood vessel:	n/a
46	chr14:105766987-105767037	K562	blood:	n/a
47	chr14:105766991-105767041	HCPEpiC	choroid plexus:	n/a
48	chr14:105766991-105767041	HCF	heart:	n/a
49	chr14:105766991-105767041	PFSK-1	brain:	n/a
50	chr14:105766987-105767037	AoSMC	blood vessel:	n/a

No.	Distal block	Cell Line	Cell type
1	chr14:105766350..105771356-chr14:105955110..105959126,6	MCF-7	breast:
2	chr14:105765282..105769482-chr14:105778355..105784135,18	K562	blood:
3	chr14:105766401..105768254-chr14:105864654..105866501,3	MCF-7	breast:
4	chr14:105766164..105768024-chr14:105938486..105941026,2	MCF-7	breast:
5	chr14:105766778..105767468-chr16:88717407..88718073,2	Hela-S3	cervix:
6	chr14:105265110..105267765-chr14:105766806..105769681,2	K562	blood:
7	chr14:105765307..105769571-chr14:105774220..105784135,13	K562	blood:
8	chr14:105443928..105445902-chr14:105765680..105767557,2	MCF-7	breast:
9	chr14:105766490..105767158-chr17:41465540..41466173,2	Hela-S3	cervix:
10	chr14:105765913..105767563-chr14:105954548..105956473,2	MCF-7	breast:
11	chr14:105713379..105716522-chr14:105764463..105769159,4	MCF-7	breast:

Variant related genes	Relation type
BRF1	TF binding region
BRF1	CpG island
ENSG00000051523	Chromatin interaction
ENSG00000184887	Chromatin interaction
ENSG00000188825	Chromatin interaction
ENSG00000182809	Chromatin interaction
ENSG00000179364	Chromatin interaction
ENSG00000185567	Chromatin interaction
ENSG00000257341	Chromatin interaction
ENSG00000185347	Chromatin interaction
ENSG00000185024	Chromatin interaction
ENSG00000179627	Chromatin interaction
ENSG00000226174	Chromatin interaction

Extended variants
information (count: 23 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:23 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv1828345	chr14:105100787-105803170	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	165 gene(s)	inside rSNPs	diseases
2	nsv542225	chr14:105133688-105803170	Enhancers Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Weak transcription Active TSS Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	165 gene(s)	inside rSNPs	diseases
3	nsv542227	chr14:105157572-105803170	Enhancers Flanking Active TSS Genic enhancers Weak transcription Active TSS Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	147 gene(s)	inside rSNPs	diseases
4	nsv917106	chr14:105339195-105803170	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer Bivalent/Poised TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	94 gene(s)	inside rSNPs	diseases
5	nsv902422	chr14:105420215-105803170	Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Active TSS Genic enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	88 gene(s)	inside rSNPs	diseases
6	nsv902423	chr14:105430890-105803170	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription Strong transcription Genic enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	88 gene(s)	inside rSNPs	diseases
7	nsv902424	chr14:105436222-105803170	Genic enhancers Weak transcription Enhancers Bivalent Enhancer Strong transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	86 gene(s)	inside rSNPs	diseases
8	esv2758369	chr14:105513346-105803170	Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Active TSS Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
9	esv2760014	chr14:105513346-105803170	Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
10	nsv902441	chr14:105602619-105803170	Active TSS Enhancers Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Weak transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
11	nsv902442	chr14:105602619-105803170	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
12	esv1817919	chr14:105605199-105803170	Enhancers Active TSS Weak transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
13	nsv530813	chr14:105607701-106453697	Strong transcription Weak transcription Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	149 gene(s)	inside rSNPs	diseases
14	nsv566186	chr14:105675701-105779305	Weak transcription Strong transcription Flanking Active TSS Enhancers Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
15	nsv902466	chr14:105704465-105803170	Active TSS Weak transcription Enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
16	esv29986	chr14:105707292-105803170	Flanking Active TSS Active TSS Enhancers Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
17	nsv832887	chr14:105717339-105803170	Strong transcription Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
18	nsv832888	chr14:105717339-105803170	Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Strong transcription Active TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
19	nsv1049929	chr14:105718240-105772037	Enhancers Strong transcription Flanking Active TSS Weak transcription Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	15 gene(s)	inside rSNPs	diseases
20	nsv1052355	chr14:105718240-105789157	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	17 gene(s)	inside rSNPs	diseases
21	nsv566187	chr14:105756485-105780704	Weak transcription Flanking Active TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	15 gene(s)	inside rSNPs	diseases
22	esv3420807	chr14:105764707-105769605	Flanking Active TSS Active TSS Weak transcription Transcr. at gene 5' and 3' Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	13 gene(s)	inside rSNPs	diseases
23	esv3380677	chr14:105766332-105769080	Active TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	13 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:127 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:105765600-105767000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
2	chr14:105765600-105767000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr14:105765600-105767000	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
4	chr14:105765600-105768400	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr14:105765800-105768400	Active TSS	A549	lung
6	chr14:105766000-105768000	Active TSS	GM12878-XiMat	blood
7	chr14:105766000-105768000	Active TSS	HSMMtube	muscle
8	chr14:105766000-105768200	Active TSS	Pancreatic Islets	Pancreatic Islet
9	chr14:105766000-105768200	Active TSS	HSMM	muscle
10	chr14:105766000-105768200	Active TSS	NHDF-Ad	bronchial
11	chr14:105766000-105768400	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
12	chr14:105766200-105767000	Flanking Active TSS	Primary mononuclear cells fromperipheralblood	Blood
13	chr14:105766200-105768000	Active TSS	Ovary	ovary
14	chr14:105766200-105768000	Bivalent/Poised TSS	HepG2	liver
15	chr14:105766200-105768200	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr14:105766200-105768200	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
17	chr14:105766200-105768200	Active TSS	NHLF	lung
18	chr14:105766200-105768400	Active TSS	H9 Cell Line	embryonic stem cell
19	chr14:105766200-105768400	Active TSS	Lung	lung
20	chr14:105766400-105768000	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr14:105766400-105768000	Active TSS	Brain Anterior Caudate	brain
22	chr14:105766400-105768000	Active TSS	Brain Cingulate Gyrus	brain
23	chr14:105766400-105768000	Active TSS	Brain Substantia Nigra	brain
24	chr14:105766400-105768000	Active TSS	Stomach Mucosa	stomach
25	chr14:105766400-105768000	Active TSS	Hela-S3	cervix
26	chr14:105766400-105768000	Active TSS	NH-A	brain
27	chr14:105766400-105768200	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr14:105766400-105768200	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
29	chr14:105766400-105768200	Active TSS	Muscle Satellite Cultured Cells	--
30	chr14:105766400-105768200	Active TSS	Aorta	Aorta
31	chr14:105766400-105768200	Active TSS	Brain Angular Gyrus	brain
32	chr14:105766400-105768200	Active TSS	Colon Smooth Muscle	Colon
33	chr14:105766400-105768200	Active TSS	Duodenum Smooth Muscle	Duodenum
34	chr14:105766400-105768200	Active TSS	Fetal Kidney	kidney
35	chr14:105766400-105768200	Active TSS	Fetal Lung	lung
36	chr14:105766400-105768200	Active TSS	NHEK	skin
37	chr14:105766400-105768400	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
38	chr14:105766400-105768400	Active TSS	Brain Hippocampus Middle	brain
39	chr14:105766400-105768600	Active TSS	K562	blood
40	chr14:105766600-105767000	Bivalent/Poised TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
41	chr14:105766600-105767000	Active TSS	Fetal Heart	heart
42	chr14:105766600-105767200	Transcr. at gene 5' and 3'	iPS DF 19.11 Cell Line	embryonic stem cell
43	chr14:105766600-105767600	Transcr. at gene 5' and 3'	Primary T helper 17 cells PMA-I stimulated	--
44	chr14:105766600-105767600	Active TSS	Monocytes-CD14+_RO01746	blood
45	chr14:105766600-105767800	Active TSS	Primary T cells fromperipheralblood	blood
46	chr14:105766600-105767800	Active TSS	Primary hematopoietic stem cells	blood
47	chr14:105766600-105767800	Active TSS	Primary T helper memory cells from peripheral blood 2	blood
48	chr14:105766600-105767800	Active TSS	Primary T helper naive cells from peripheral blood	blood
49	chr14:105766600-105767800	Active TSS	Primary T helper cells PMA-I stimulated	--
50	chr14:105766600-105767800	Active TSS	Fetal Muscle Trunk	muscle

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