Variant report

Variant	rs3809470
Chromosome Location	chr14:105531945-105531946
allele	C/T
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	POU2F2	chr14:105531488-105532819	GM12891	blood:	n/a	chr14:105532074-105532086 chr14:105532310-105532322 chr14:105531682-105531694 chr14:105532237-105532249
2	TAF1	chr14:105531545-105532154	GM12878	blood:	n/a	n/a
3	POLR2A	chr14:105529893-105533288	GM12891	blood:	n/a	n/a
4	SRF	chr14:105531644-105532073	GM12878	blood:	n/a	n/a
5	RCOR1	chr14:105531724-105531983	K562	blood:	n/a	n/a
6	REST	chr14:105531523-105532497	HL-60	blood:	n/a	chr14:105532199-105532219 chr14:105532202-105532215 chr14:105532438-105532451 chr14:105532204-105532213
7	SP1	chr14:105531540-105532093	GM12878	blood:	n/a	chr14:105531642-105531656
8	FOS	chr14:105531755-105531996	MCF10A-Er-Src	breast:	n/a	chr14:105531953-105531964
9	TAF1	chr14:105531119-105532204	GM12878	blood:	n/a	n/a
10	ZEB1	chr14:105531668-105532171	GM12878	blood:	n/a	n/a
11	MEF2A	chr14:105531528-105532170	GM12878	blood:	n/a	n/a
12	EBF1	chr14:105531638-105532080	GM12878	blood:	n/a	n/a
13	ELF1	chr14:105531571-105532102	GM12878	blood:	n/a	chr14:105531770-105531783
14	FOXM1	chr14:105531517-105532174	GM12878	blood:	n/a	n/a
15	NFYB	chr14:105531041-105532031	GM12878	blood:	n/a	chr14:105531329-105531344 chr14:105531329-105531344 chr14:105531328-105531340
16	TCF12	chr14:105531581-105532409	GM12878	blood:	n/a	n/a
17	EP300	chr14:105531045-105532124	GM12878	blood:	n/a	chr14:105531994-105532010
18	POLR2A	chr14:105530960-105534026	GM18526	blood:	n/a	n/a
19	RCOR1	chr14:105531111-105532401	GM12878	blood:	n/a	n/a
20	POLR2A	chr14:105524383-105533160	GM12891	blood:	n/a	n/a
21	POLR2A	chr14:105530869-105533961	GM12878	blood:	n/a	n/a
22	YY1	chr14:105530915-105533143	GM12892	blood:	n/a	chr14:105532806-105532828 chr14:105532343-105532354 chr14:105531133-105531147 chr14:105531647-105531658 chr14:105532804-105532823 chr14:105531582-105531592
23	PBX3	chr14:105531602-105532065	GM12878	blood:	n/a	n/a
24	RELA	chr14:105531610-105532288	GM18526	blood:	n/a	n/a
25	PAX5	chr14:105531633-105532123	GM12878	blood:	n/a	n/a
26	CTCF	chr14:105531920-105532070	A549	lung:	n/a	n/a
27	POLR2A	chr14:105530997-105533349	GM15510	blood:	n/a	n/a
28	PAX5	chr14:105531903-105532299	GM12892	blood:	n/a	n/a
29	TBP	chr14:105531102-105532358	GM12878	blood:	n/a	n/a
30	SRF	chr14:105531748-105532100	GM12878	blood:	n/a	n/a
31	SPI1	chr14:105531534-105532086	HL-60	blood:	n/a	chr14:105531625-105531638
32	BCL3	chr14:105531569-105532133	GM12878	blood:	n/a	n/a
33	ATF2	chr14:105531529-105532220	GM12878	blood:	n/a	n/a
34	POLR2A	chr14:105531060-105533127	GM10847	blood:	n/a	n/a
35	FOS	chr14:105531730-105532067	MCF10A-Er-Src	breast:	n/a	chr14:105531953-105531964
36	IKZF1	chr14:105529970-105532541	GM12878	blood:	n/a	n/a
37	TCF3	chr14:105531607-105532095	GM12878	blood:	n/a	chr14:105531993-105532003
38	ATF1	chr14:105531689-105532059	K562	blood:	n/a	n/a
39	PAX5	chr14:105531664-105531951	GM12878	blood:	n/a	n/a
40	POLR2A	chr14:105530891-105532639	HL-60	blood:	n/a	n/a
41	CHD2	chr14:105531069-105533914	GM12878	blood:	n/a	n/a
42	CEBPB	chr14:105531084-105532171	GM12878	blood:	n/a	n/a
43	POLR2A	chr14:105531659-105532207	NB4	blood:	n/a	n/a
44	POU2F2	chr14:105531569-105532242	GM12878	blood:	n/a	chr14:105532074-105532086 chr14:105531682-105531694
45	PAX5	chr14:105531600-105532071	GM12892	blood:	n/a	n/a
46	ZNF143	chr14:105531571-105532278	GM12878	blood:	n/a	chr14:105531634-105531652
47	POLR2A	chr14:105530908-105533385	GM12878	blood:	n/a	n/a
48	EP300	chr14:105531730-105531977	K562	blood:	n/a	n/a
49	EP300	chr14:105531086-105532160	GM12878	blood:	n/a	chr14:105531994-105532010
50	TAF1	chr14:105531541-105532218	GM12892	blood:	n/a	n/a

Variant related genes	Relation type
GPR132	TF binding region

Extended variants
information (count: 70 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:45)

rs_ID	r²[population]
rs10147672	0.83[JPT][hapmap]
rs10151777	0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11627133	0.98[GIH][hapmap];0.87[MEX][hapmap];0.89[TSI][hapmap];0.83[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs12433746	1.00[CEU][hapmap];1.00[CHB][hapmap];0.97[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12436511	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12889428	0.85[CHB][hapmap];0.87[AMR][1000 genomes];0.93[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs12895274	0.83[AMR][1000 genomes]
rs28664663	0.88[AFR][1000 genomes];0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs34116292	0.83[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs34878850	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34882611	0.87[AMR][1000 genomes]
rs35886229	0.97[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs35966880	0.95[AFR][1000 genomes];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3809464	0.86[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs3809465	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs3809466	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs3809469	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs3825765	0.94[EUR][1000 genomes]
rs4265748	0.82[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4288933	0.84[ASW][hapmap];1.00[CEU][hapmap];0.90[CHB][hapmap];0.95[GIH][hapmap];0.88[LWK][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.82[YRI][hapmap];0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4377097	0.90[CHB][hapmap];0.81[JPT][hapmap]
rs4391998	0.91[CEU][hapmap];0.97[TSI][hapmap];0.94[EUR][1000 genomes]
rs4457938	0.92[EUR][1000 genomes]
rs4464021	0.88[CEU][hapmap];0.90[CHB][hapmap];0.81[JPT][hapmap];0.82[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs4581644	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs55780149	0.87[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs55951335	0.89[AMR][1000 genomes]
rs56159244	0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs56275808	0.89[AMR][1000 genomes]
rs60562761	0.87[EUR][1000 genomes]
rs61997788	0.81[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs61997789	0.81[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs7144647	0.91[CEU][hapmap];0.88[CHB][hapmap];0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7145885	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs7147439	0.83[CEU][hapmap];0.97[TSI][hapmap];0.96[EUR][1000 genomes]
rs7147669	0.84[ASW][hapmap];0.91[CEU][hapmap];0.90[CHB][hapmap];0.95[GIH][hapmap];0.84[LWK][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.88[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs7152235	0.91[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7152401	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7157567	0.84[ASW][hapmap];0.91[CEU][hapmap];0.90[CHB][hapmap];0.95[GIH][hapmap];0.84[LWK][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.88[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs7158479	0.90[CHB][hapmap];0.83[GIH][hapmap];1.00[MEX][hapmap]
rs7160811	0.81[GIH][hapmap];0.96[MEX][hapmap]
rs8011909	0.86[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs8015942	0.92[MEX][hapmap]
rs8018607	0.90[CHB][hapmap];0.83[CHD][hapmap];0.87[JPT][hapmap];0.92[MEX][hapmap]
rs8020062	0.89[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]

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	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	nsv456457	chr14:105404384-105555396	Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Strong transcription Weak transcription Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	63 gene(s)	inside rSNPs	diseases
6	nsv566141	chr14:105404384-105555396	Weak transcription Flanking Bivalent TSS/Enh Active TSS Enhancers Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	63 gene(s)	inside rSNPs	diseases
7	nsv902421	chr14:105410183-105574843	Weak transcription Enhancers Genic enhancers Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer 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	73 gene(s)	inside rSNPs	diseases
8	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
9	nsv1052190	chr14:105423761-105722653	Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	81 gene(s)	inside rSNPs	diseases
10	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
11	nsv1042303	chr14:105435649-105633544	Bivalent Enhancer Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription Active TSS ZNF genes & repeats Strong transcription Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	73 gene(s)	inside rSNPs	diseases
12	nsv456458	chr14:105435649-105690092	Flanking Active TSS Weak transcription Enhancers Bivalent Enhancer Strong transcription Active TSS Bivalent/Poised TSS 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	77 gene(s)	inside rSNPs	diseases
13	nsv566150	chr14:105435649-105690092	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Active TSS Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	77 gene(s)	inside rSNPs	diseases
14	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
15	nsv566151	chr14:105459140-105555396	Flanking Active TSS Weak transcription Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
16	nsv456459	chr14:105459140-105617891	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	55 gene(s)	inside rSNPs	diseases
17	nsv566152	chr14:105459140-105617891	Weak transcription Bivalent Enhancer Genic enhancers Strong transcription Enhancers Active TSS ZNF genes & repeats Flanking 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	55 gene(s)	inside rSNPs	diseases
18	nsv902425	chr14:105463936-105690092	Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Weak transcription ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Strong transcription 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
19	nsv983941	chr14:105485574-105534240	Enhancers Active TSS Flanking Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	37 gene(s)	inside rSNPs	diseases
20	nsv9175	chr14:105496509-105688941	Enhancers Strong transcription Bivalent/Poised TSS Active TSS Weak transcription Bivalent Enhancer ZNF genes & repeats Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
21	nsv902426	chr14:105500760-105537476	Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription Genic enhancers Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
22	nsv902427	chr14:105508577-105585347	Enhancers Flanking Active TSS Bivalent/Poised TSS Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
23	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
24	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
25	nsv902428	chr14:105531945-105555396	Bivalent/Poised TSS Flanking Active TSS Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs3809470	TRMT61A	cis	parietal	SCAN
rs3809470	AHNAK2	cis	cerebellum	SCAN

Chromatin state (count:73 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:105525600-105534200	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
2	chr14:105525800-105533400	Weak transcription	Osteobl	bone
3	chr14:105526400-105532800	Flanking Active TSS	Primary T cells fromperipheralblood	blood
4	chr14:105528800-105532000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr14:105528800-105532000	Weak transcription	Right Ventricle	heart
6	chr14:105528800-105542000	Weak transcription	Right Atrium	heart
7	chr14:105529600-105532800	Flanking Active TSS	Primary B cells from cord blood	blood
8	chr14:105530400-105532000	Active TSS	Rectal Mucosa Donor 29	rectum
9	chr14:105530400-105532200	Active TSS	Brain Hippocampus Middle	brain
10	chr14:105530400-105532400	Active TSS	Rectal Smooth Muscle	rectum
11	chr14:105530400-105532600	Flanking Active TSS	Primary Natural Killer cells fromperipheralblood	blood
12	chr14:105530600-105532000	Active TSS	Brain Cingulate Gyrus	brain
13	chr14:105530600-105532600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
14	chr14:105530800-105532000	Active TSS	Primary T helper memory cells from peripheral blood 2	blood
15	chr14:105530800-105532000	Active TSS	Primary T killer memory cells from peripheral blood	blood
16	chr14:105530800-105532000	Active TSS	Colonic Mucosa	Colon
17	chr14:105530800-105532000	Active TSS	Monocytes-CD14+_RO01746	blood
18	chr14:105530800-105532400	Active TSS	Esophagus	oesophagus
19	chr14:105531000-105532000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
20	chr14:105531000-105532000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr14:105531000-105532000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
22	chr14:105531000-105532000	Active TSS	Stomach Smooth Muscle	stomach
23	chr14:105531000-105532200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
24	chr14:105531000-105532200	Flanking Active TSS	Fetal Thymus	thymus
25	chr14:105531000-105532200	Active TSS	Sigmoid Colon	Sigmoid Colon
26	chr14:105531000-105532200	Enhancers	Stomach Mucosa	stomach
27	chr14:105531000-105532400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr14:105531000-105532400	Active TSS	Rectal Mucosa Donor 31	rectum
29	chr14:105531000-105532600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
30	chr14:105531000-105532600	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
31	chr14:105531000-105532600	Enhancers	NH-A	brain
32	chr14:105531000-105532800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
33	chr14:105531000-105534400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
34	chr14:105531000-105534600	Enhancers	Spleen	Spleen
35	chr14:105531200-105532400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
36	chr14:105531200-105533000	Enhancers	Lung	lung
37	chr14:105531400-105532000	Active TSS	Primary monocytes fromperipheralblood	blood
38	chr14:105531400-105532000	Active TSS	Primary T helper naive cells from peripheral blood	blood
39	chr14:105531400-105532000	Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
40	chr14:105531400-105532000	Active TSS	Primary T killer naive cells fromperipheralblood	blood
41	chr14:105531400-105532000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
42	chr14:105531400-105532000	Enhancers	HSMMtube	muscle
43	chr14:105531400-105532600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
44	chr14:105531400-105542800	Weak transcription	Gastric	stomach
45	chr14:105531600-105532000	Active TSS	Primary neutrophils fromperipheralblood	blood
46	chr14:105531600-105532000	Active TSS	Primary B cells from peripheral blood	blood
47	chr14:105531600-105532000	Active TSS	Primary T cells from cord blood	blood
48	chr14:105531600-105532000	Enhancers	Primary hematopoietic stem cells	blood
49	chr14:105531600-105532000	Enhancers	Primary hematopoietic stem cells short term culture	blood
50	chr14:105531600-105532000	Active TSS	Primary T helper naive cells fromperipheralblood	blood

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