Variant report

Variant	rs542228931
Chromosome Location	chr14:105266681-105266682
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	CTCF	chr14:105266600-105266750	HRPEpiC	eye:	n/a	chr14:105266716-105266725
2	ZC3H11A	chr14:105266616-105266688	K562	blood:	n/a	n/a
3	CTCFL	chr14:105266593-105266799	K562	blood:	n/a	n/a
4	CTCF	chr14:105266540-105266690	GM12872	blood:	n/a	n/a
5	CTCF	chr14:105266608-105266828	Pancreas_OC	pancreas:	n/a	chr14:105266716-105266725
6	CTCF	chr14:105266660-105266810	HA-sp	spinal cord:	n/a	chr14:105266716-105266725
7	CTCF	chr14:105266560-105266710	HFF-Myc	foreskin:	n/a	n/a
8	CTCF	chr14:105266620-105266770	AoAF	blood vessel:	n/a	chr14:105266716-105266725
9	MAFK	chr14:105266572-105266691	K562	blood:	n/a	n/a
10	MYC	chr14:105266504-105267873	K562	blood:	n/a	n/a
11	ZBTB7A	chr14:105265894-105267034	ECC-1	luminal epithelium:	n/a	chr14:105266444-105266455
12	CTCF	chr14:105266620-105266770	Hela-S3	cervix:	n/a	chr14:105266716-105266725
13	TCF12	chr14:105266486-105267966	ECC-1	luminal epithelium:	n/a	n/a
14	EGR1	chr14:105266595-105266888	GM12878	blood:	n/a	chr14:105266673-105266686 chr14:105266673-105266686
15	CTCF	chr14:105266640-105266790	GM12875	blood:	n/a	chr14:105266716-105266725
16	CTCF	chr14:105266660-105266810	GM12878	blood:	n/a	chr14:105266716-105266725
17	CTCF	chr14:105266640-105266790	GM12869	blood:	n/a	chr14:105266716-105266725
18	CHD2	chr14:105266585-105266852	Hela-S3	cervix:	n/a	chr14:105266658-105266667
19	CTCF	chr14:105266640-105266790	GM12874	blood:	n/a	chr14:105266716-105266725
20	CTCF	chr14:105266640-105266790	AG04449	skin:	n/a	chr14:105266716-105266725
21	TBL1XR1	chr14:105266545-105266912	K562	blood:	n/a	n/a
22	CTCF	chr14:105266577-105266822	HepG2	liver:	n/a	chr14:105266716-105266725
23	TBP	chr14:105266502-105266768	H1-hESC	embryonic stem cell:	n/a	n/a
24	CTCF	chr14:105266632-105266837	Kidney_OC	kidney:	n/a	chr14:105266716-105266725
25	CTCF	chr14:105266640-105266790	K562	blood:	n/a	chr14:105266716-105266725
26	CTCF	chr14:105266675-105266777	H1-hESC	embryonic stem cell:	n/a	chr14:105266716-105266725
27	EP300	chr14:105266577-105266896	SK-N-SH_RA	brain:	n/a	chr14:105266870-105266879
28	JUND	chr14:105266665-105266783	H1-hESC	embryonic stem cell:	n/a	n/a
29	MAZ	chr14:105265714-105267436	HepG2	liver:	n/a	n/a
30	CTCF	chr14:105266513-105266913	K562	blood:	n/a	chr14:105266716-105266725
31	MXI1	chr14:105266645-105266777	K562	blood:	n/a	n/a
32	CTCF	chr14:105266640-105266790	GM12872	blood:	n/a	chr14:105266716-105266725
33	NR2F2	chr14:105266541-105266748	K562	blood:	n/a	n/a
34	CTCF	chr14:105266580-105266730	GM12865	blood:	n/a	chr14:105266716-105266725
35	CTCF	chr14:105266640-105266790	HUVEC	blood vessel:	n/a	chr14:105266716-105266725
36	POLR2A	chr14:105266443-105266770	HepG2	liver:	n/a	n/a
37	CTCF	chr14:105266660-105266810	NHDF-neo	bronchial:	n/a	chr14:105266716-105266725
38	CTCF	chr14:105266640-105266790	AG09319	gingival:	n/a	chr14:105266716-105266725
39	CHD2	chr14:105266449-105266847	GM12878	blood:	n/a	chr14:105266658-105266667
40	CTCF	chr14:105266643-105266850	Spleen_OC	spleen:	n/a	chr14:105266716-105266725
41	CTCF	chr14:105266600-105266750	AG09309	skin:	n/a	chr14:105266716-105266725
42	CTCF	chr14:105266511-105266908	K562	blood:	n/a	chr14:105266716-105266725
43	PAX5	chr14:105266650-105267056	GM12892	blood:	n/a	n/a
44	ELF1	chr14:105266475-105267031	GM12878	blood:	n/a	n/a
45	CTCF	chr14:105266640-105266790	GM12865	blood:	n/a	chr14:105266716-105266725
46	CTCF	chr14:105266660-105266810	GM12865	blood:	n/a	chr14:105266716-105266725
47	CTCF	chr14:105266600-105266750	AG10803	skin:	n/a	chr14:105266716-105266725
48	CTCF	chr14:105266600-105266750	GM12864	blood:	n/a	chr14:105266716-105266725
49	POLR2A	chr14:105266681-105266730	ProgFib	skin:	n/a	n/a
50	CHD2	chr14:105266068-105266896	HepG2	liver:	n/a	chr14:105266860-105266870 chr14:105266658-105266667 chr14:105266855-105266865

No.	Distal block	Cell Line	Cell type
1	chr14:105265965..105267568-chr14:105442748..105445496,2	MCF-7	breast:
2	chr14:105217901..105222027-chr14:105264438..105269623,6	K562	blood:
3	chr14:105188315..105194275-chr14:105263600..105268559,9	MCF-7	breast:
4	chr14:105259095..105269353-chr14:105280422..105289302,26	K562	blood:
5	chr14:105151580..105154010-chr14:105263839..105266807,2	MCF-7	breast:
6	chr14:105217632..105222660-chr14:105263642..105269157,6	K562	blood:
7	chr14:104576831..104579461-chr14:105265082..105267856,2	MCF-7	breast:
8	chr14:105265057..105267677-chr3:49054198..49056753,2	MCF-7	breast:
9	chr14:105264532..105267379-chr14:105360102..105364298,4	MCF-7	breast:
10	chr14:105266435..105267408-chr14:105286766..105287693,2	MCF-7	breast:
11	chr14:105266268..105268334-chr14:105486957..105488737,2	K562	blood:
12	chr14:105265825..105268360-chr14:105330933..105332611,2	K562	blood:
13	chr14:105190071..105193724-chr14:105262102..105266779,4	K562	blood:
14	chr14:105188668..105192164-chr14:105264427..105268088,6	MCF-7	breast:
15	chr14:105265912..105268902-chr14:105329301..105333250,7	MCF-7	breast:
16	chr14:105265110..105267765-chr14:105766806..105769681,2	K562	blood:
17	chr14:105175368..105177558-chr14:105266041..105268999,2	MCF-7	breast:
18	chr14:105264903..105267195-chr14:105323456..105325361,2	MCF-7	breast:
19	chr14:105216947..105220630-chr14:105265563..105270028,6	MCF-7	breast:

Variant related genes	Relation type
ZBTB42	TF binding region
AKT1	TF binding region
ENSG00000258593	Chromatin interaction
ENSG00000178149	Chromatin interaction
ENSG00000099814	Chromatin interaction
ENSG00000185100	Chromatin interaction
ENSG00000184990	Chromatin interaction
ENSG00000185024	Chromatin interaction
ENSG00000258701	Chromatin interaction
ENSG00000166183	Chromatin interaction
ENSG00000170779	Chromatin interaction
ENSG00000185567	Chromatin interaction
ENSG00000203485	Chromatin interaction
ENSG00000179364	Chromatin interaction

Extended variants
information (count: 38 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:38 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv530812	chr14:104775571-105364883	Genic enhancers Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Weak transcription Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	98 gene(s)	inside rSNPs	diseases
2	nsv1053591	chr14:105024558-105475931	Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Strong transcription Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	114 gene(s)	inside rSNPs	diseases
3	nsv542224	chr14:105024558-105475931	Bivalent Enhancer Active TSS Weak transcription Strong transcription Flanking Active TSS Enhancers Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	114 gene(s)	inside rSNPs	diseases
4	esv2830002	chr14:105078251-105348552	Enhancers Flanking Bivalent TSS/Enh Strong transcription Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	88 gene(s)	inside rSNPs	diseases
5	nsv902379	chr14:105086475-105274093	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	60 gene(s)	inside rSNPs	diseases
6	nsv902387	chr14:105092479-105274093	Flanking Active TSS Genic enhancers Enhancers Weak transcription Strong transcription Bivalent Enhancer Active TSS ZNF genes & repeats 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	60 gene(s)	inside rSNPs	diseases
7	nsv902388	chr14:105092479-105311249	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	77 gene(s)	inside rSNPs	diseases
8	nsv902389	chr14:105092479-105366499	Flanking Active TSS Enhancers Weak transcription Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	91 gene(s)	inside rSNPs	diseases
9	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
10	nsv902392	chr14:105105769-105274093	Enhancers Bivalent Enhancer Flanking Active TSS Genic enhancers Weak transcription Strong transcription ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	59 gene(s)	inside rSNPs	diseases
11	nsv902394	chr14:105116232-105274093	Flanking Active TSS Weak transcription Strong transcription Enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Genic 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	59 gene(s)	inside rSNPs	diseases
12	nsv902396	chr14:105119897-105274093	Transcr. at gene 5' and 3' Active TSS Strong transcription Flanking Active TSS Genic enhancers Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	59 gene(s)	inside rSNPs	diseases
13	nsv566052	chr14:105126354-105268228	Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	56 gene(s)	inside rSNPs	diseases
14	nsv470677	chr14:105126354-105348552	Enhancers Flanking Active TSS Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	87 gene(s)	inside rSNPs	diseases
15	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
16	nsv566053	chr14:105139894-105268228	Active TSS Flanking Active TSS Enhancers Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	56 gene(s)	inside rSNPs	diseases
17	nsv902397	chr14:105139894-105268228	Flanking Active TSS Weak transcription Active TSS Enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Strong transcription Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	56 gene(s)	inside rSNPs	diseases
18	nsv517038	chr14:105146579-105311249	Flanking Active TSS Enhancers Strong transcription Genic enhancers Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	69 gene(s)	inside rSNPs	diseases
19	nsv566057	chr14:105146579-105311249	Weak transcription Genic enhancers Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	69 gene(s)	inside rSNPs	diseases
20	nsv566059	chr14:105148655-105268228	Strong transcription Weak transcription Enhancers Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	46 gene(s)	inside rSNPs	diseases
21	nsv566060	chr14:105148655-105311249	Flanking Active TSS Genic enhancers Enhancers Bivalent Enhancer Strong transcription Weak transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	66 gene(s)	inside rSNPs	diseases
22	nsv902404	chr14:105148655-105311249	Weak transcription Flanking Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' Active TSS Enhancers Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	66 gene(s)	inside rSNPs	diseases
23	nsv902405	chr14:105148655-105340643	Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Enhancers Strong transcription Active TSS Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	77 gene(s)	inside rSNPs	diseases
24	nsv902407	chr14:105154105-105268228	Flanking Active TSS Enhancers Weak transcription Active TSS Genic enhancers Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
25	nsv902408	chr14:105154105-105274093	Active TSS ZNF genes & repeats Flanking Active TSS Enhancers Bivalent Enhancer Weak transcription Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	46 gene(s)	inside rSNPs	diseases
26	nsv902409	chr14:105154105-105311249	Flanking Active TSS Genic enhancers Weak transcription Enhancers Strong transcription Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	63 gene(s)	inside rSNPs	diseases
27	nsv566063	chr14:105154105-105312935	Weak transcription Active TSS Enhancers Genic enhancers Bivalent Enhancer Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	63 gene(s)	inside rSNPs	diseases
28	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
29	nsv902411	chr14:105163532-105268228	Weak transcription Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
30	nsv566069	chr14:105185666-105274538	Bivalent/Poised TSS Enhancers Genic enhancers Weak transcription Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
31	nsv902412	chr14:105238701-105361934	Weak transcription Enhancers Strong transcription Bivalent Enhancer Flanking Active TSS Active TSS Genic enhancers 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	53 gene(s)	inside rSNPs	diseases
32	nsv566071	chr14:105242831-105274763	Active TSS Bivalent/Poised TSS Genic enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
33	nsv566072	chr14:105245251-105274712	Enhancers Weak transcription Bivalent Enhancer Genic enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
34	esv1836552	chr14:105246686-105348552	Bivalent/Poised TSS Flanking Active TSS Enhancers Active TSS Weak transcription Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	51 gene(s)	inside rSNPs	diseases
35	nsv902413	chr14:105246686-105366499	Flanking Active TSS Active TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers Strong transcription Bivalent Enhancer Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	54 gene(s)	inside rSNPs	diseases
36	nsv902414	chr14:105246989-105274093	Bivalent/Poised TSS Flanking Active TSS Weak transcription Strong transcription Active TSS Enhancers Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
37	nsv902415	chr14:105250045-105270554	Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Enhancers Weak transcription Genic enhancers Bivalent Enhancer Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
38	esv3379257	chr14:105265732-105268280	Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Active TSS Bivalent/Poised TSS Enhancers Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	15 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	chr14:105263000-105267200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
2	chr14:105264800-105267200	Weak transcription	Gastric	stomach
3	chr14:105265800-105267400	Active TSS	HUES6 Cell Line	embryonic stem cell
4	chr14:105265800-105268200	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
5	chr14:105266000-105266800	Flanking Active TSS	Primary hematopoietic stem cells	blood
6	chr14:105266000-105266800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr14:105266000-105266800	Flanking Active TSS	Fetal Muscle Leg	muscle
8	chr14:105266000-105266800	Flanking Bivalent TSS/Enh	Monocytes-CD14+_RO01746	blood
9	chr14:105266000-105267600	Bivalent/Poised TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
10	chr14:105266000-105267600	Active TSS	H9 Cell Line	embryonic stem cell
11	chr14:105266000-105267600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr14:105266000-105267600	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
13	chr14:105266000-105267600	Bivalent/Poised TSS	Thymus	Thymus
14	chr14:105266000-105267800	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
15	chr14:105266000-105267800	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
16	chr14:105266000-105268000	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
17	chr14:105266000-105268200	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
18	chr14:105266200-105266800	Flanking Active TSS	Primary B cells from peripheral blood	blood
19	chr14:105266200-105266800	Flanking Active TSS	Primary T cells fromperipheralblood	blood
20	chr14:105266200-105266800	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
21	chr14:105266200-105266800	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
22	chr14:105266200-105266800	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
23	chr14:105266200-105266800	Flanking Active TSS	Primary Natural Killer cells fromperipheralblood	blood
24	chr14:105266200-105266800	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin01	Skin
25	chr14:105266200-105266800	Flanking Bivalent TSS/Enh	Brain Germinal Matrix	brain
26	chr14:105266200-105266800	Enhancers	Brain Substantia Nigra	brain
27	chr14:105266200-105266800	Flanking Active TSS	Fetal Adrenal Gland	Adrenal Gland
28	chr14:105266200-105266800	Flanking Bivalent TSS/Enh	Fetal Thymus	thymus
29	chr14:105266200-105267200	Enhancers	Primary B cells from cord blood	blood
30	chr14:105266200-105267600	Active TSS	ES-WA7 Cell Line	embryonic stem cell
31	chr14:105266200-105267600	Active TSS	Brain Inferior Temporal Lobe	brain
32	chr14:105266200-105267800	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
33	chr14:105266200-105267800	Bivalent/Poised TSS	Fetal Brain Female	brain
34	chr14:105266200-105268000	Active TSS	Aorta	Aorta
35	chr14:105266400-105266800	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
36	chr14:105266400-105266800	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
37	chr14:105266400-105266800	Flanking Active TSS	Placenta	Placenta
38	chr14:105266400-105267000	Weak transcription	Spleen	Spleen
39	chr14:105266400-105267400	Bivalent/Poised TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
40	chr14:105266400-105267600	Active TSS	Duodenum Smooth Muscle	Duodenum
41	chr14:105266400-105267600	Active TSS	Ovary	ovary
42	chr14:105266400-105267600	Active TSS	Rectal Smooth Muscle	rectum
43	chr14:105266400-105267600	Active TSS	NHLF	lung
44	chr14:105266400-105267800	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
45	chr14:105266400-105267800	Active TSS	Primary T killer naive cells fromperipheralblood	blood
46	chr14:105266400-105267800	Active TSS	Small Intestine	intestine
47	chr14:105266400-105267800	Active TSS	HepG2	liver
48	chr14:105266400-105267800	Active TSS	NHDF-Ad	bronchial
49	chr14:105266400-105268000	Active TSS	Pancreatic Islets	Pancreatic Islet
50	chr14:105266600-105267200	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell

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