Variant report

Variant	rs587624456
Chromosome Location	chr14:105768057-105768058
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	MAX	chr14:105767738-105768281	ECC-1	luminal epithelium:	n/a	chr14:105767916-105767926 chr14:105767844-105767854 chr14:105767751-105767761 chr14:105767785-105767795
2	CREB1	chr14:105766729-105768188	A549	lung:	n/a	n/a
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	POLR2A	chr14:105766819-105768162	HepG2	liver:	n/a	n/a
6	ZBTB7A	chr14:105766992-105768258	ECC-1	luminal epithelium:	n/a	n/a
7	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
8	SP1	chr14:105767234-105768288	H1-hESC	embryonic stem cell:	n/a	chr14:105767845-105767854 chr14:105767750-105767762 chr14:105767843-105767855 chr14:105767784-105767795 chr14:105767720-105767732 chr14:105767916-105767925 chr14:105767784-105767796 chr14:105767717-105767731 chr14:105767720-105767731 chr14:105767722-105767731 chr14:105767916-105767926 chr14:105767659-105767669 chr14:105767750-105767761 chr14:105767720-105767732 chr14:105767751-105767760 chr14:105767750-105767762 chr14:105767917-105767926 chr14:105767658-105767670 chr14:105767659-105767669 chr14:105767843-105767855 chr14:105767844-105767854 chr14:105767660-105767669 chr14:105767784-105767796 chr14:105767911-105767920 chr14:105767658-105767670 chr14:105767648-105767662 chr14:105767916-105767930 chr14:105767785-105767794 chr14:105767708-105767718 chr14:105767915-105767927 chr14:105767659-105767668 chr14:105767751-105767761 chr14:105767785-105767795 chr14:105767660-105767669 chr14:105767785-105767795 chr14:105767709-105767718 chr14:105767844-105767854 chr14:105767655-105767669 chr14:105767915-105767927 chr14:105767751-105767761 chr14:105767721-105767730 chr14:105767514-105767526 chr14:105767708-105767717 chr14:105767752-105767761 chr14:105767844-105767853 chr14:105767514-105767526 chr14:105767781-105767795 chr14:105767786-105767795
9	HCFC1	chr14:105765946-105768196	Hela-S3	cervix:	n/a	n/a
10	POLR2A	chr14:105766762-105768115	MCF10A-Er-Src	breast:	n/a	n/a
11	JUND	chr14:105767990-105768190	HepG2	liver:	n/a	chr14:105768054-105768065 chr14:105768056-105768067 chr14:105768058-105768067 chr14:105768056-105768068
12	RCOR1	chr14:105766667-105768078	GM12878	blood:	n/a	n/a
13	GABPA	chr14:105767774-105768141	H1-hESC	embryonic stem cell:	n/a	chr14:105767785-105767794 chr14:105767844-105767853
14	MAX	chr14:105768039-105768224	A549	lung:	n/a	n/a
15	E2F6	chr14:105768003-105768200	K562	blood:	n/a	n/a
16	ZBTB7A	chr14:105767050-105768186	ECC-1	luminal epithelium:	n/a	n/a
17	HMGN3	chr14:105766757-105768119	K562	blood:	n/a	n/a
18	E2F6	chr14:105767859-105768271	H1-hESC	embryonic stem cell:	n/a	n/a
19	HEY1	chr14:105767814-105768093	K562	blood:	n/a	n/a
20	POLR2A	chr14:105766865-105768162	HCT-116	colon:	n/a	n/a
21	MXI1	chr14:105766108-105768085	GM12878	blood:	n/a	n/a
22	POLR2A	chr14:105767787-105768163	K562	blood:	n/a	n/a
23	POLR2A	chr14:105766753-105768219	HUVEC	blood vessel:	n/a	n/a
24	POLR2A	chr14:105766625-105768562	K562	blood:	n/a	n/a
25	ELF1	chr14:105767044-105768277	MCF-7	breast:	n/a	chr14:105767705-105767717 chr14:105767826-105767838 chr14:105767917-105767929
26	MAX	chr14:105767982-105768236	K562	blood:	n/a	n/a
27	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
28	CCNT2	chr14:105766686-105768120	K562	blood:	n/a	chr14:105767659-105767668
29	SP1	chr14:105767172-105768214	A549	lung:	n/a	chr14:105767845-105767854 chr14:105767750-105767762 chr14:105767843-105767855 chr14:105767784-105767795 chr14:105767720-105767732 chr14:105767916-105767925 chr14:105767784-105767796 chr14:105767717-105767731 chr14:105767720-105767731 chr14:105767722-105767731 chr14:105767916-105767926 chr14:105767659-105767669 chr14:105767750-105767761 chr14:105767720-105767732 chr14:105767751-105767760 chr14:105767750-105767762 chr14:105767917-105767926 chr14:105767658-105767670 chr14:105767659-105767669 chr14:105767843-105767855 chr14:105767844-105767854 chr14:105767660-105767669 chr14:105767784-105767796 chr14:105767911-105767920 chr14:105767658-105767670 chr14:105767648-105767662 chr14:105767916-105767930 chr14:105767785-105767794 chr14:105767708-105767718 chr14:105767915-105767927 chr14:105767659-105767668 chr14:105767751-105767761 chr14:105767785-105767795 chr14:105767660-105767669 chr14:105767785-105767795 chr14:105767709-105767718 chr14:105767844-105767854 chr14:105767655-105767669 chr14:105767915-105767927 chr14:105767751-105767761 chr14:105767721-105767730 chr14:105767514-105767526 chr14:105767708-105767717 chr14:105767752-105767761 chr14:105767844-105767853 chr14:105767514-105767526 chr14:105767781-105767795 chr14:105767786-105767795
30	ZBTB7A	chr14:105767009-105768207	K562	blood:	n/a	n/a
31	EP300	chr14:105768041-105768120	GM12878	blood:	n/a	n/a
32	NRF1	chr14:105767877-105768119	H1-hESC	embryonic stem cell:	n/a	n/a
33	USF2	chr14:105768040-105768060	H1-hESC	embryonic stem cell:	n/a	n/a
34	SP1	chr14:105767163-105768077	HepG2	liver:	n/a	chr14:105767845-105767854 chr14:105767750-105767762 chr14:105767843-105767855 chr14:105767784-105767795 chr14:105767720-105767732 chr14:105767916-105767925 chr14:105767784-105767796 chr14:105767717-105767731 chr14:105767720-105767731 chr14:105767722-105767731 chr14:105767916-105767926 chr14:105767659-105767669 chr14:105767750-105767761 chr14:105767720-105767732 chr14:105767751-105767760 chr14:105767750-105767762 chr14:105767917-105767926 chr14:105767658-105767670 chr14:105767659-105767669 chr14:105767843-105767855 chr14:105767844-105767854 chr14:105767660-105767669 chr14:105767784-105767796 chr14:105767911-105767920 chr14:105767658-105767670 chr14:105767648-105767662 chr14:105767916-105767930 chr14:105767785-105767794 chr14:105767708-105767718 chr14:105767915-105767927 chr14:105767659-105767668 chr14:105767751-105767761 chr14:105767785-105767795 chr14:105767660-105767669 chr14:105767785-105767795 chr14:105767709-105767718 chr14:105767844-105767854 chr14:105767655-105767669 chr14:105767915-105767927 chr14:105767751-105767761 chr14:105767721-105767730 chr14:105767514-105767526 chr14:105767708-105767717 chr14:105767752-105767761 chr14:105767844-105767853 chr14:105767514-105767526 chr14:105767781-105767795 chr14:105767786-105767795
35	POLR2A	chr14:105766720-105768148	K562	blood:	n/a	n/a
36	MAX	chr14:105766332-105768240	HepG2	liver:	n/a	chr14:105767652-105767662 chr14:105767916-105767926 chr14:105767844-105767854 chr14:105767708-105767718 chr14:105766553-105766562 chr14:105767751-105767761 chr14:105767785-105767795
37	NR2F2	chr14:105767403-105768419	K562	blood:	n/a	n/a
38	STAT3	chr14:105768015-105768215	MCF10A-Er-Src	breast:	n/a	n/a
39	POLR2A	chr14:105767109-105768242	SK-N-MC	brain:	n/a	n/a
40	RUNX3	chr14:105765930-105768251	GM12878	blood:	n/a	chr14:105766729-105766746
41	TAL1	chr14:105767899-105768099	K562	blood:	n/a	n/a
42	POLR2A	chr14:105767820-105768113	K562	blood:	n/a	n/a
43	MAX	chr14:105766474-105768234	MCF-7	breast:	n/a	chr14:105767652-105767662 chr14:105767916-105767926 chr14:105767844-105767854 chr14:105767708-105767718 chr14:105766553-105766562 chr14:105767751-105767761 chr14:105767785-105767795
44	TAF1	chr14:105766530-105768067	HepG2	liver:	n/a	n/a
45	BHLHE40	chr14:105767853-105768215	K562	blood:	n/a	n/a
46	MAX	chr14:105766228-105768274	A549	lung:	n/a	chr14:105767652-105767662 chr14:105767916-105767926 chr14:105767844-105767854 chr14:105767708-105767718 chr14:105766553-105766562 chr14:105767751-105767761 chr14:105767785-105767795
47	ZNF143	chr14:105767996-105768089	K562	blood:	n/a	n/a
48	TBP	chr14:105766558-105768322	K562	blood:	n/a	n/a
49	MAX	chr14:105767823-105768277	H1-hESC	embryonic stem cell:	n/a	chr14:105767916-105767926 chr14:105767844-105767854
50	MYC	chr14:105766557-105768208	K562	blood:	n/a	chr14:105767652-105767662 chr14:105767916-105767926 chr14:105767844-105767854 chr14:105767708-105767718 chr14:105767751-105767761 chr14:105767785-105767795

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	chr14:105767766..105768456-chr14:105800435..105801361,2	MCF-7	breast:
5	chr14:105265110..105267765-chr14:105766806..105769681,2	K562	blood:
6	chr14:105765307..105769571-chr14:105774220..105784135,13	K562	blood:
7	chr14:23540375..23540895-chr14:105767305..105768183,2	HCT-116	colon:
8	chr14:105713379..105716522-chr14:105764463..105769159,4	MCF-7	breast:

Variant related genes	Relation type
BRF1	TF binding region
ENSG00000184887	Chromatin interaction
ENSG00000226174	Chromatin interaction
ENSG00000185347	Chromatin interaction
ENSG00000100813	Chromatin interaction
ENSG00000179364	Chromatin interaction
ENSG00000179627	Chromatin interaction
ENSG00000185024	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:125 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:105765600-105768400	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr14:105765800-105768400	Active TSS	A549	lung
3	chr14:105766000-105768200	Active TSS	Pancreatic Islets	Pancreatic Islet
4	chr14:105766000-105768200	Active TSS	HSMM	muscle
5	chr14:105766000-105768200	Active TSS	NHDF-Ad	bronchial
6	chr14:105766000-105768400	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
7	chr14:105766200-105768200	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr14:105766200-105768200	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
9	chr14:105766200-105768200	Active TSS	NHLF	lung
10	chr14:105766200-105768400	Active TSS	H9 Cell Line	embryonic stem cell
11	chr14:105766200-105768400	Active TSS	Lung	lung
12	chr14:105766400-105768200	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr14:105766400-105768200	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr14:105766400-105768200	Active TSS	Muscle Satellite Cultured Cells	--
15	chr14:105766400-105768200	Active TSS	Aorta	Aorta
16	chr14:105766400-105768200	Active TSS	Brain Angular Gyrus	brain
17	chr14:105766400-105768200	Active TSS	Colon Smooth Muscle	Colon
18	chr14:105766400-105768200	Active TSS	Duodenum Smooth Muscle	Duodenum
19	chr14:105766400-105768200	Active TSS	Fetal Kidney	kidney
20	chr14:105766400-105768200	Active TSS	Fetal Lung	lung
21	chr14:105766400-105768200	Active TSS	NHEK	skin
22	chr14:105766400-105768400	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
23	chr14:105766400-105768400	Active TSS	Brain Hippocampus Middle	brain
24	chr14:105766400-105768600	Active TSS	K562	blood
25	chr14:105766600-105768200	Active TSS	ES-WA7 Cell Line	embryonic stem cell
26	chr14:105766600-105768200	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
27	chr14:105766600-105768200	Active TSS	Primary T cells from cord blood	blood
28	chr14:105766600-105768200	Active TSS	Brain Germinal Matrix	brain
29	chr14:105766600-105768200	Active TSS	Fetal Brain Female	brain
30	chr14:105766600-105768200	Active TSS	Fetal Intestine Large	intestine
31	chr14:105766600-105768200	Active TSS	Fetal Intestine Small	intestine
32	chr14:105766600-105768200	Active TSS	Gastric	stomach
33	chr14:105766600-105768200	Active TSS	Psoas Muscle	Psoas
34	chr14:105766600-105768200	Active TSS	Small Intestine	intestine
35	chr14:105766600-105768400	Active TSS	HUES48 Cell Line	embryonic stem cell
36	chr14:105766600-105768400	Active TSS	iPS-18 Cell Line	embryonic stem cell
37	chr14:105766600-105768400	Active TSS	iPS-20b Cell Line	embryonic stem cell
38	chr14:105766600-105768400	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
39	chr14:105766600-105768400	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
40	chr14:105766600-105768400	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
41	chr14:105766600-105768400	Active TSS	Brain Inferior Temporal Lobe	brain
42	chr14:105766600-105768400	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
43	chr14:105766600-105768400	Active TSS	Duodenum Mucosa	Duodenum
44	chr14:105766600-105768400	Active TSS	Fetal Adrenal Gland	Adrenal Gland
45	chr14:105766600-105768400	Active TSS	Rectal Mucosa Donor 29	rectum
46	chr14:105766600-105768400	Active TSS	Rectal Smooth Muscle	rectum
47	chr14:105766600-105768600	Active TSS	HUES64 Cell Line	embryonic stem cell
48	chr14:105766600-105768600	Active TSS	iPS-15b Cell Line	embryonic stem cell
49	chr14:105766800-105768200	Active TSS	Esophagus	oesophagus
50	chr14:105766800-105768400	Active TSS	ES-I3 Cell Line	embryonic stem cell

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