Variant report

Variant	rs861539
Chromosome Location	chr14:104165753-104165754
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:64)
CpG islands
(count:0)
Chromatin interactive
region (count:1)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:64 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr14:104161808-104167956	GM12891	blood:	n/a	n/a
2	POLR2A	chr14:104165092-104166064	Hela-S3	cervix:	n/a	n/a
3	POLR2A	chr14:104162428-104167912	GM12892	blood:	n/a	n/a
4	POLR2A	chr14:104163629-104167827	GM12892	blood:	n/a	n/a
5	POLR2A	chr14:104163960-104166036	GM12878	blood:	n/a	n/a
6	POLR2A	chr14:104163159-104166993	GM15510	blood:	n/a	n/a
7	BCL3	chr14:104165009-104166292	A549	lung:	n/a	n/a
8	POLR2A	chr14:104163444-104167238	K562	blood:	n/a	n/a
9	POLR2A	chr14:104164696-104167900	GM12892	blood:	n/a	n/a
10	POLR2A	chr14:104163620-104167914	Hela-S3	cervix:	n/a	n/a
11	POLR2A	chr14:104162433-104167795	PANC-1	pancreas:	n/a	n/a
12	POLR2A	chr14:104163591-104166090	K562	blood:	n/a	n/a
13	POLR2A	chr14:104163817-104166083	GM18526	blood:	n/a	n/a
14	POLR2A	chr14:104165247-104165985	HUVEC	blood vessel:	n/a	n/a
15	POLR2A	chr14:104163893-104166055	GM12878	blood:	n/a	n/a
16	POLR2A	chr14:104163557-104168043	K562	blood:	n/a	n/a
17	POLR2A	chr14:104164050-104165998	ECC-1	luminal epithelium:	n/a	n/a
18	POLR2A	chr14:104165164-104165925	GM12892	blood:	n/a	n/a
19	JUND	chr14:104165032-104165867	A549	lung:	n/a	n/a
20	POLR2A	chr14:104163958-104166014	A549	lung:	n/a	n/a
21	POLR2A	chr14:104163459-104166880	HepG2	liver:	n/a	n/a
22	POLR2A	chr14:104163873-104167654	GM12878	blood:	n/a	n/a
23	POLR2A	chr14:104163748-104165986	HEK293	kidney:	n/a	n/a
24	POLR2A	chr14:104163442-104166908	GM12891	blood:	n/a	n/a
25	POLR2A	chr14:104163614-104166779	K562	blood:	n/a	n/a
26	POLR2A	chr14:104161885-104167797	K562	blood:	n/a	n/a
27	HMGN3	chr14:104165122-104165888	K562	blood:	n/a	n/a
28	POLR2A	chr14:104163379-104165855	PFSK-1	brain:	n/a	n/a
29	POLR2A	chr14:104165004-104166207	ProgFib	skin:	n/a	n/a
30	POLR2A	chr14:104162049-104167862	K562	blood:	n/a	n/a
31	POLR2A	chr14:104158412-104167854	Hela-S3	cervix:	n/a	n/a
32	POLR2A	chr14:104163610-104167839	GM19193	blood:	n/a	n/a
33	POLR2A	chr14:104163355-104167291	H1-hESC	embryonic stem cell:	n/a	n/a
34	POLR2A	chr14:104163780-104167919	GM12892	blood:	n/a	n/a
35	POLR2A	chr14:104163545-104165779	H1-hESC	embryonic stem cell:	n/a	n/a
36	POLR2A	chr14:104163700-104167829	GM18951	blood:	n/a	n/a
37	POLR2A	chr14:104165705-104167795	K562	blood:	n/a	n/a
38	POLR2A	chr14:104164764-104166081	HL-60	blood:	n/a	n/a
39	POLR2A	chr14:104163531-104166608	PFSK-1	brain:	n/a	n/a
40	NFATC1	chr14:104165713-104166470	GM12878	blood:	n/a	n/a
41	POLR2A	chr14:104163810-104167414	GM12878	blood:	n/a	n/a
42	POLR2A	chr14:104161823-104167781	GM12878	blood:	n/a	n/a
43	POLR2A	chr14:104163586-104165947	HL-60	blood:	n/a	n/a
44	POLR2A	chr14:104163650-104166855	GM19099	blood:	n/a	n/a
45	POLR2A	chr14:104163619-104166133	Hela-S3	cervix:	n/a	n/a
46	POLR2A	chr14:104161532-104176510	SK-N-MC	brain:	n/a	n/a
47	MTA3	chr14:104162445-104165839	GM12878	blood:	n/a	n/a
48	POLR2A	chr14:104162516-104167394	K562	blood:	n/a	n/a
49	POLR2A	chr14:104162273-104167865	MCF-7	breast:	n/a	n/a
50	POLR2A	chr14:104163384-104167654	H1-hESC	embryonic stem cell:	n/a	n/a

No data

(count:1 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr14:104094584..104096859-chr14:104165203..104168753,3	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000269910	TF binding region
KLC1	TF binding region
ENSG00000126214	Chromatin interaction

Extended variants
information (count: 61 )
Associated
traits (count: 10 )

rSNPs within LD-proxies of this variant (count:37)

rs_ID	r²[population]
rs10134399	0.83[ASW][hapmap];0.88[CEU][hapmap];0.94[GIH][hapmap];0.91[JPT][hapmap];0.89[TSI][hapmap];0.82[YRI][hapmap];0.81[EUR][1000 genomes]
rs10135248	0.96[CEU][hapmap];1.00[GIH][hapmap];0.91[JPT][hapmap];1.00[MEX][hapmap];0.93[TSI][hapmap];0.85[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs10143623	0.81[AFR][1000 genomes];0.97[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs10145755	0.90[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs10147049	0.92[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs10149249	0.91[ASW][hapmap];0.84[CEU][hapmap];0.84[GIH][hapmap];0.91[JPT][hapmap];0.84[LWK][hapmap];0.87[TSI][hapmap]
rs11622552	0.83[JPT][hapmap]
rs11624505	0.86[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs11627794	0.92[ASN][1000 genomes]
rs11849259	0.89[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs2274268	0.84[CEU][hapmap];0.91[JPT][hapmap]
rs2403205	1.00[ASW][hapmap];0.96[CEU][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];0.90[MKK][hapmap];0.95[TSI][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs3783404	0.96[CEU][hapmap];1.00[JPT][hapmap];0.82[YRI][hapmap];0.90[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs3915733	0.95[AFR][1000 genomes];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs55864158	0.81[AFR][1000 genomes]
rs55885592	0.81[AFR][1000 genomes];0.89[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs56660916	0.81[AFR][1000 genomes];0.90[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs57218990	0.97[AFR][1000 genomes];0.90[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs58133129	0.87[AFR][1000 genomes];0.88[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs61995780	0.95[AFR][1000 genomes];0.90[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs6593	0.95[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs68087451	0.88[AFR][1000 genomes];0.82[EUR][1000 genomes]
rs709400	1.00[ASW][hapmap];0.96[CEU][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];0.90[MKK][hapmap];0.95[TSI][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs7150141	0.96[CEU][hapmap];1.00[GIH][hapmap];0.91[JPT][hapmap];1.00[MEX][hapmap];0.93[TSI][hapmap];0.87[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs7154948	0.84[CEU][hapmap];0.84[GIH][hapmap];0.91[JPT][hapmap];0.83[MEX][hapmap];0.89[TSI][hapmap]
rs7359090	0.88[AFR][1000 genomes];0.94[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs7693	0.84[CEU][hapmap];0.84[GIH][hapmap];0.91[JPT][hapmap];0.83[MEX][hapmap];0.89[TSI][hapmap]
rs8003090	0.88[AFR][1000 genomes]
rs8005885	0.90[AFR][1000 genomes];0.90[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs8018979	0.88[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs861528	1.00[JPT][hapmap]
rs861531	0.96[CEU][hapmap];1.00[GIH][hapmap];0.91[JPT][hapmap];1.00[MEX][hapmap];0.93[TSI][hapmap];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs861534	0.95[CEU][hapmap];0.82[CHB][hapmap];0.90[JPT][hapmap];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs861536	1.00[ASW][hapmap];0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];0.93[TSI][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs861538	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs861548	0.92[AFR][1000 genomes];0.93[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs942863	0.84[CEU][hapmap];0.84[GIH][hapmap];0.91[JPT][hapmap];0.83[MEX][hapmap];0.89[TSI][hapmap]

Variant overlapped rSNPs/rCNVs (count:24 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3332028	chr14:103581471-104328811	Weak transcription Active TSS Enhancers Strong transcription Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	162 gene(s)	inside rSNPs	diseases
2	nsv902300	chr14:103967504-104205811	Active TSS Enhancers Bivalent Enhancer Flanking Active TSS Genic enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	83 gene(s)	inside rSNPs	diseases
3	nsv1052010	chr14:104061472-104216267	Weak transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription Enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	52 gene(s)	inside rSNPs	diseases
4	nsv542201	chr14:104061472-104216267	Weak transcription Enhancers Genic enhancers Strong transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	52 gene(s)	inside rSNPs	diseases
5	nsv456435	chr14:104061646-104198251	Weak transcription Genic enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	52 gene(s)	inside rSNPs	diseases
6	nsv566023	chr14:104061646-104198251	Strong transcription Enhancers Weak transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	52 gene(s)	inside rSNPs	diseases
7	nsv902308	chr14:104087209-104211180	Enhancers Genic enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	52 gene(s)	inside rSNPs	diseases
8	nsv1041329	chr14:104097750-104196346	Strong transcription Weak transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	38 gene(s)	inside rSNPs	diseases
9	nsv542202	chr14:104097750-104196346	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	38 gene(s)	inside rSNPs	diseases
10	nsv1048866	chr14:104100862-104195896	Weak transcription Active TSS Flanking Active TSS Genic enhancers Strong transcription Enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	38 gene(s)	inside rSNPs	diseases
11	nsv1045162	chr14:104140525-104594841	Flanking Active TSS Strong transcription Bivalent Enhancer Enhancers Active TSS Weak transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	87 gene(s)	inside rSNPs	diseases
12	nsv542204	chr14:104140525-104594841	Active TSS Enhancers Strong transcription Weak transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	87 gene(s)	inside rSNPs	diseases
13	nsv1041347	chr14:104141217-104186372	Weak transcription Enhancers Strong transcription Active TSS Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	36 gene(s)	inside rSNPs	diseases
14	nsv902309	chr14:104143385-104198251	Strong transcription Weak transcription Enhancers Genic enhancers ZNF genes & repeats Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	36 gene(s)	inside rSNPs	diseases
15	nsv902310	chr14:104143385-104205811	Genic enhancers Active TSS Transcr. at gene 5' and 3' Enhancers Strong transcription Flanking Active TSS Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
16	esv2758368	chr14:104147525-104412813	Active TSS Weak transcription Genic enhancers Enhancers Flanking Active TSS Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	56 gene(s)	inside rSNPs	diseases
17	esv2760013	chr14:104147525-104412813	Enhancers Genic enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS 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	56 gene(s)	inside rSNPs	diseases
18	nsv902311	chr14:104148339-104205811	Flanking Active TSS Enhancers Weak transcription Strong transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
19	nsv902312	chr14:104155317-104211180	Strong transcription Flanking Active TSS Genic enhancers Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
20	esv1796914	chr14:104159882-104181369	Strong transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Active TSS Weak transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
21	nsv527425	chr14:104162263-104198251	Transcr. at gene 5' and 3' Genic enhancers Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	29 gene(s)	inside rSNPs	diseases
22	nsv470673	chr14:104162263-104219949	Enhancers Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
23	nsv902313	chr14:104162263-104378087	Bivalent Enhancer Genic enhancers Strong transcription Weak transcription Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	48 gene(s)	inside rSNPs	diseases
24	nsv902314	chr14:104163901-104170465	Strong transcription Genic enhancers Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

mRNA abundance (count:10)

SNP	Gene	Cis/trans	Tissue	Source
rs861539	DNAH8	trans	parietal	SCAN
rs861539	DIO3	cis	cerebellum	SCAN
rs861539	ZFYVE21	cis	cerebellum	SCAN
rs861539	APOPT1	cis	Muscle Skeletal	GTEx
rs861539	C14orf153	cis	parietal	SCAN
rs861539	MARK3	cis	Thyroid	GTEx
rs861539	BAG5	cis	multi-tissue	Pritchard
rs861539	BAG5	Cis_1M	lymphoblastoid	RTeQTL
rs861539	BAG5	cis	cerebellum	SCAN
rs861539	KLC1	cis	parietal	SCAN

Chromatin state (count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:104117800-104176000	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
2	chr14:104118800-104175600	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
3	chr14:104119200-104173000	Strong transcription	Primary T helper cells fromperipheralblood	blood
4	chr14:104119400-104175200	Strong transcription	Primary neutrophils fromperipheralblood	blood
5	chr14:104120000-104177000	Strong transcription	HUES64 Cell Line	embryonic stem cell
6	chr14:104124600-104169800	Strong transcription	Primary monocytes fromperipheralblood	blood
7	chr14:104124600-104169800	Strong transcription	Monocytes-CD14+_RO01746	blood
8	chr14:104133400-104177200	Strong transcription	iPS-20b Cell Line	embryonic stem cell
9	chr14:104135600-104177600	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr14:104146200-104174800	Weak transcription	K562	blood
11	chr14:104152600-104178600	Weak transcription	Small Intestine	intestine
12	chr14:104157400-104167600	Genic enhancers	Placenta	Placenta
13	chr14:104158200-104169000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
14	chr14:104158200-104170200	Genic enhancers	Fetal Muscle Leg	muscle
15	chr14:104158400-104167800	Strong transcription	Primary T cells from cord blood	blood
16	chr14:104158400-104171200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
17	chr14:104158400-104178000	Strong transcription	Dnd41	blood
18	chr14:104158600-104176400	Strong transcription	H9 Cell Line	embryonic stem cell
19	chr14:104159800-104176200	Strong transcription	Sigmoid Colon	Sigmoid Colon
20	chr14:104160200-104167000	Strong transcription	HMEC	breast
21	chr14:104161000-104167200	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
22	chr14:104161000-104170600	Weak transcription	Pancreatic Islets	Pancreatic Islet
23	chr14:104161000-104176600	Genic enhancers	Spleen	Spleen
24	chr14:104161200-104165800	Genic enhancers	Lung	lung
25	chr14:104161200-104166000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
26	chr14:104161200-104180000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
27	chr14:104161200-104180400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
28	chr14:104161800-104165800	Genic enhancers	Fetal Thymus	thymus
29	chr14:104161800-104166000	Enhancers	Primary B cells from cord blood	blood
30	chr14:104161800-104167800	Genic enhancers	Right Ventricle	heart
31	chr14:104162000-104169600	Genic enhancers	Primary B cells from peripheral blood	blood
32	chr14:104162200-104165800	Genic enhancers	Rectal Mucosa Donor 29	rectum
33	chr14:104162400-104172400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
34	chr14:104162800-104177200	Strong transcription	HUES6 Cell Line	embryonic stem cell
35	chr14:104163000-104165800	Genic enhancers	Gastric	stomach
36	chr14:104163000-104167200	Weak transcription	Primary T helper cells PMA-I stimulated	--
37	chr14:104163200-104165800	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
38	chr14:104163200-104169000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr14:104163400-104166200	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
40	chr14:104163400-104166200	Genic enhancers	Brain Cingulate Gyrus	brain
41	chr14:104163400-104166400	Genic enhancers	Brain Hippocampus Middle	brain
42	chr14:104163400-104172600	Genic enhancers	Fetal Muscle Trunk	muscle
43	chr14:104163400-104176800	Strong transcription	H1 Cell Line	embryonic stem cell
44	chr14:104163400-104177200	Strong transcription	HUES48 Cell Line	embryonic stem cell
45	chr14:104163600-104166000	Genic enhancers	Skeletal Muscle Male	skeletal muscle
46	chr14:104163600-104176200	Strong transcription	Osteobl	bone
47	chr14:104163600-104177200	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
48	chr14:104163600-104177600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
49	chr14:104163800-104165800	Genic enhancers	Colonic Mucosa	Colon
50	chr14:104163800-104165800	Genic enhancers	Pancreas	Pancrea

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