Variant report

Variant	rs2295145
Chromosome Location	chr14:104202304-104202305
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:9)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:104190417..104195099-chr14:104198034..104202895,6	MCF-7	breast:
2	chr14:104200638..104203848-chr14:104208638..104212508,3	MCF-7	breast:
3	chr14:104199732..104203374-chr14:104205758..104208488,4	MCF-7	breast:
4	chr14:104182025..104183554-chr14:104201618..104203977,2	MCF-7	breast:
5	chr14:104196893..104198671-chr14:104201327..104203237,2	K562	blood:
6	chr14:104201896..104204456-chr14:104312035..104314445,3	MCF-7	breast:
7	chr14:104187861..104189972-chr14:104201127..104202685,2	MCF-7	breast:
8	chr14:104202267..104204342-chr14:104211278..104213145,2	MCF-7	breast:
9	chr14:104195030..104198558-chr14:104199394..104203156,3	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000258735	Chromatin interaction
ENSG00000100711	Chromatin interaction
ENSG00000253096	Chromatin interaction
ENSG00000088808	Chromatin interaction

Extended variants
information (count: 119 )
Associated
traits (count: 3 )

rSNPs within LD-proxies of this variant (count:105)

rs_ID	r²[population]
rs10083367	0.81[EUR][1000 genomes]
rs10135720	0.80[YRI][hapmap]
rs10140452	0.82[YRI][hapmap]
rs1040813	1.00[CEU][hapmap];1.00[YRI][hapmap];0.84[EUR][1000 genomes]
rs10873539	0.84[EUR][1000 genomes]
rs11160758	0.94[AFR][1000 genomes];0.98[EUR][1000 genomes]
rs11160759	1.00[CEU][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];0.96[EUR][1000 genomes]
rs11160760	0.94[ASW][hapmap];1.00[CEU][hapmap];0.88[GIH][hapmap];0.96[LWK][hapmap];0.81[MKK][hapmap];0.95[TSI][hapmap];1.00[YRI][hapmap];0.88[AFR][1000 genomes];0.89[EUR][1000 genomes]
rs11160761	0.87[AFR][1000 genomes];0.89[EUR][1000 genomes]
rs11160762	0.94[ASW][hapmap];1.00[CEU][hapmap];0.89[GIH][hapmap];0.98[LWK][hapmap];0.81[MKK][hapmap];0.95[TSI][hapmap];1.00[YRI][hapmap];0.88[AFR][1000 genomes];0.89[EUR][1000 genomes]
rs11160765	0.84[EUR][1000 genomes]
rs1155751	1.00[CEU][hapmap];0.90[CHB][hapmap];0.85[EUR][1000 genomes]
rs11623546	0.94[ASW][hapmap];1.00[CEU][hapmap];0.89[GIH][hapmap];0.95[LWK][hapmap];0.95[TSI][hapmap];1.00[YRI][hapmap];0.88[EUR][1000 genomes]
rs11624184	0.94[ASW][hapmap];1.00[CEU][hapmap];0.86[GIH][hapmap];0.93[TSI][hapmap];1.00[YRI][hapmap];0.90[AFR][1000 genomes];0.96[EUR][1000 genomes]
rs11625740	0.96[CEU][hapmap];0.89[CHB][hapmap];0.83[CHD][hapmap];0.85[GIH][hapmap];0.95[TSI][hapmap];0.96[EUR][1000 genomes]
rs11626377	1.00[CEU][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];0.96[EUR][1000 genomes]
rs11628240	0.94[AFR][1000 genomes];0.98[EUR][1000 genomes]
rs11628332	0.94[ASW][hapmap];1.00[CEU][hapmap];0.89[GIH][hapmap];0.98[LWK][hapmap];0.81[MKK][hapmap];0.95[TSI][hapmap];1.00[YRI][hapmap];0.91[AFR][1000 genomes];0.96[EUR][1000 genomes]
rs11628481	0.91[AFR][1000 genomes];0.96[EUR][1000 genomes]
rs11847468	0.94[ASW][hapmap];1.00[CEU][hapmap];0.89[GIH][hapmap];0.98[LWK][hapmap];0.81[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];0.98[EUR][1000 genomes]
rs1187416	1.00[CEU][hapmap];0.84[EUR][1000 genomes]
rs12433109	0.89[ASW][hapmap];0.81[CEU][hapmap];0.94[LWK][hapmap];0.89[MKK][hapmap];0.83[YRI][hapmap];0.83[AFR][1000 genomes]
rs12434686	0.84[EUR][1000 genomes]
rs12588489	0.91[AFR][1000 genomes];0.95[EUR][1000 genomes]
rs12878682	0.93[AFR][1000 genomes];0.96[EUR][1000 genomes]
rs12878868	0.88[AFR][1000 genomes];0.96[EUR][1000 genomes]
rs12879501	0.94[ASW][hapmap];1.00[CEU][hapmap];0.89[GIH][hapmap];0.98[LWK][hapmap];0.80[MKK][hapmap];0.95[TSI][hapmap];1.00[YRI][hapmap];0.80[AFR][1000 genomes];0.88[EUR][1000 genomes]
rs12879612	0.95[EUR][1000 genomes]
rs12880167	0.84[EUR][1000 genomes]
rs12880233	0.86[EUR][1000 genomes]
rs12880368	0.84[EUR][1000 genomes]
rs12880413	0.87[EUR][1000 genomes]
rs12880821	1.00[CEU][hapmap];0.90[CHB][hapmap];0.88[EUR][1000 genomes]
rs12885018	1.00[CEU][hapmap];1.00[YRI][hapmap];0.80[AFR][1000 genomes];0.88[EUR][1000 genomes]
rs12886840	0.84[EUR][1000 genomes]
rs12889993	0.94[ASW][hapmap];1.00[CEU][hapmap];0.89[GIH][hapmap];0.96[LWK][hapmap];0.80[MKK][hapmap];0.95[TSI][hapmap];1.00[YRI][hapmap];0.80[AFR][1000 genomes];0.88[EUR][1000 genomes]
rs12891175	0.94[ASW][hapmap];1.00[CEU][hapmap];0.89[GIH][hapmap];0.98[LWK][hapmap];0.80[MKK][hapmap];0.95[TSI][hapmap];1.00[YRI][hapmap];0.80[AFR][1000 genomes];0.88[EUR][1000 genomes]
rs12891589	0.93[AFR][1000 genomes];0.95[EUR][1000 genomes]
rs12894254	0.85[EUR][1000 genomes]
rs12897150	0.83[EUR][1000 genomes]
rs1475007	0.94[ASW][hapmap];1.00[CEU][hapmap];0.89[GIH][hapmap];0.98[LWK][hapmap];0.80[MKK][hapmap];0.95[TSI][hapmap];1.00[YRI][hapmap];0.84[EUR][1000 genomes]
rs1535097	0.94[ASW][hapmap];1.00[CEU][hapmap];0.89[GIH][hapmap];0.98[LWK][hapmap];0.83[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes];0.98[EUR][1000 genomes]
rs1535098	1.00[CEU][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];0.98[EUR][1000 genomes]
rs1547604	0.89[CEU][hapmap]
rs1955660	0.89[CEU][hapmap]
rs1997913	0.94[ASW][hapmap];0.96[CEU][hapmap];0.85[GIH][hapmap];0.91[LWK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];0.98[EUR][1000 genomes]
rs2024667	0.83[AFR][1000 genomes];0.97[EUR][1000 genomes]
rs2024669	0.89[CEU][hapmap]
rs2223937	0.83[ASW][hapmap];1.00[CEU][hapmap];0.89[GIH][hapmap];0.91[LWK][hapmap];0.95[TSI][hapmap];0.93[YRI][hapmap];0.86[EUR][1000 genomes]
rs2295140	0.89[CEU][hapmap];0.80[AMR][1000 genomes]
rs2295141	0.94[ASW][hapmap];1.00[CEU][hapmap];0.89[GIH][hapmap];0.98[LWK][hapmap];0.83[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes];0.98[EUR][1000 genomes]
rs2295146	0.85[CEU][hapmap];0.81[GIH][hapmap];0.87[LWK][hapmap];0.86[TSI][hapmap];0.86[EUR][1000 genomes]
rs2368560	1.00[CEU][hapmap];0.90[CHB][hapmap];0.80[YRI][hapmap];0.88[EUR][1000 genomes]
rs28533661	0.81[EUR][1000 genomes]
rs28698555	0.84[EUR][1000 genomes]
rs2887282	0.94[ASW][hapmap];1.00[CEU][hapmap];0.89[GIH][hapmap];0.98[LWK][hapmap];0.80[MKK][hapmap];0.95[TSI][hapmap];1.00[YRI][hapmap];0.87[EUR][1000 genomes]
rs34066659	0.86[EUR][1000 genomes]
rs34813623	0.83[AFR][1000 genomes];0.88[EUR][1000 genomes]
rs35505672	0.84[AFR][1000 genomes];0.88[EUR][1000 genomes]
rs3742365	0.83[ASW][hapmap];0.88[CEU][hapmap];0.81[GIH][hapmap];0.93[LWK][hapmap];0.82[MKK][hapmap];0.85[AFR][1000 genomes];0.80[EUR][1000 genomes]
rs3818085	0.94[ASW][hapmap];1.00[CEU][hapmap];0.89[GIH][hapmap];0.98[LWK][hapmap];0.83[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes];0.98[EUR][1000 genomes]
rs4900594	1.00[CEU][hapmap];0.90[CHB][hapmap];0.88[CHD][hapmap];0.86[GIH][hapmap];0.91[TSI][hapmap];0.89[EUR][1000 genomes]
rs4900595	0.83[AFR][1000 genomes];0.89[EUR][1000 genomes]
rs4900598	0.85[EUR][1000 genomes]
rs4900600	1.00[CEU][hapmap];0.90[YRI][hapmap];0.86[EUR][1000 genomes]
rs4906365	1.00[CEU][hapmap];0.85[CHB][hapmap];0.86[YRI][hapmap];0.94[EUR][1000 genomes]
rs4906371	0.87[AFR][1000 genomes];0.89[EUR][1000 genomes]
rs4906372	0.85[EUR][1000 genomes]
rs4906373	0.87[EUR][1000 genomes]
rs55824307	0.88[EUR][1000 genomes]
rs6575997	0.84[ASW][hapmap];1.00[CEU][hapmap];0.89[GIH][hapmap];0.89[LWK][hapmap];1.00[TSI][hapmap];0.82[AFR][1000 genomes];0.97[EUR][1000 genomes]
rs6575999	0.88[AFR][1000 genomes];0.89[EUR][1000 genomes]
rs6576003	0.89[CEU][hapmap]
rs66509671	0.81[AFR][1000 genomes];0.82[EUR][1000 genomes]
rs67768834	0.93[AFR][1000 genomes];0.98[EUR][1000 genomes]
rs7141473	0.84[EUR][1000 genomes]
rs7141928	0.89[CEU][hapmap];0.85[TSI][hapmap]
rs71419615	0.81[EUR][1000 genomes]
rs7147171	0.94[ASW][hapmap];1.00[CEU][hapmap];0.89[GIH][hapmap];0.98[LWK][hapmap];0.95[TSI][hapmap];1.00[YRI][hapmap];0.83[AFR][1000 genomes];0.88[EUR][1000 genomes]
rs7149024	0.95[EUR][1000 genomes]
rs7152148	0.90[AFR][1000 genomes];0.92[EUR][1000 genomes]
rs7156697	0.96[EUR][1000 genomes]
rs7156834	1.00[CEU][hapmap];0.89[CHB][hapmap];0.96[EUR][1000 genomes]
rs7159810	0.94[ASW][hapmap];1.00[CEU][hapmap];0.89[GIH][hapmap];0.98[LWK][hapmap];0.95[TSI][hapmap];1.00[YRI][hapmap];0.85[EUR][1000 genomes]
rs7401843	0.88[EUR][1000 genomes]
rs7401901	0.84[AFR][1000 genomes];0.89[EUR][1000 genomes]
rs8003653	0.94[ASW][hapmap];1.00[CEU][hapmap];0.89[GIH][hapmap];0.98[LWK][hapmap];0.95[TSI][hapmap];1.00[YRI][hapmap];0.84[EUR][1000 genomes]
rs8004408	0.94[ASW][hapmap];1.00[CEU][hapmap];0.92[GIH][hapmap];0.96[LWK][hapmap];0.92[MKK][hapmap];0.95[TSI][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];0.95[EUR][1000 genomes]
rs8005225	0.94[ASW][hapmap];1.00[CEU][hapmap];0.89[GIH][hapmap];0.98[LWK][hapmap];0.80[MKK][hapmap];0.95[TSI][hapmap];1.00[YRI][hapmap];0.84[EUR][1000 genomes]
rs8005594	1.00[CEU][hapmap];1.00[YRI][hapmap];0.87[EUR][1000 genomes]
rs8009116	0.91[AFR][1000 genomes];0.98[EUR][1000 genomes]
rs8011109	0.87[EUR][1000 genomes]
rs8011137	0.84[EUR][1000 genomes]
rs8013637	0.85[EUR][1000 genomes]
rs8014294	0.84[CEU][hapmap]
rs8015603	0.85[EUR][1000 genomes]
rs8016014	1.00[CEU][hapmap];0.85[EUR][1000 genomes]
rs8018062	0.87[EUR][1000 genomes]
rs8020234	0.85[EUR][1000 genomes]
rs8021682	0.83[EUR][1000 genomes]
rs8022783	0.88[AFR][1000 genomes];0.89[EUR][1000 genomes]
rs876002	0.94[ASW][hapmap];1.00[CEU][hapmap];0.89[GIH][hapmap];0.98[LWK][hapmap];0.81[MKK][hapmap];0.95[TSI][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];0.96[EUR][1000 genomes]
rs941473	0.82[CEU][hapmap]
rs941475	0.89[CEU][hapmap]
rs9743799	0.85[AFR][1000 genomes];0.89[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:14 , 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	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
6	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
7	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
8	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
9	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
10	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
11	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
12	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
13	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
14	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

mRNA abundance (count:3)

SNP	Gene	Cis/trans	Tissue	Source
rs2295145	INF2	cis	cerebellum	SCAN
rs2295145	DIO3	cis	cerebellum	SCAN
rs2295145	ZFYVE21	cis	cerebellum	SCAN

Chromatin state (count:121 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:104184000-104209000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr14:104184200-104214400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
3	chr14:104184400-104211000	Weak transcription	Hela-S3	cervix
4	chr14:104189400-104203200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
5	chr14:104190800-104204200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr14:104191000-104203200	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
7	chr14:104191200-104209200	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
8	chr14:104191600-104223800	Weak transcription	Pancreatic Islets	Pancreatic Islet
9	chr14:104192200-104216600	Strong transcription	Sigmoid Colon	Sigmoid Colon
10	chr14:104194000-104209200	Strong transcription	Fetal Intestine Large	intestine
11	chr14:104194200-104205600	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
12	chr14:104194200-104211400	Strong transcription	Colonic Mucosa	Colon
13	chr14:104194200-104220400	Strong transcription	Rectal Mucosa Donor 29	rectum
14	chr14:104194400-104208800	Strong transcription	Primary T cells from cord blood	blood
15	chr14:104194600-104206800	Strong transcription	Brain Germinal Matrix	brain
16	chr14:104194800-104209200	Strong transcription	Duodenum Mucosa	Duodenum
17	chr14:104194800-104209200	Strong transcription	Fetal Intestine Small	intestine
18	chr14:104194800-104212000	Strong transcription	Rectal Mucosa Donor 31	rectum
19	chr14:104195800-104215200	Weak transcription	HSMM	muscle
20	chr14:104196000-104214200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
21	chr14:104196000-104268000	Weak transcription	Small Intestine	intestine
22	chr14:104196200-104207200	Weak transcription	Primary B cells from cord blood	blood
23	chr14:104196800-104206600	Strong transcription	Thymus	Thymus
24	chr14:104197400-104204400	Weak transcription	HMEC	breast
25	chr14:104197400-104204600	Weak transcription	Stomach Mucosa	stomach
26	chr14:104197400-104204600	Weak transcription	K562	blood
27	chr14:104198000-104218800	Strong transcription	Gastric	stomach
28	chr14:104198200-104204400	Genic enhancers	Esophagus	oesophagus
29	chr14:104198200-104205200	Genic enhancers	Brain Dorsolateral Prefrontal Cortex	brain
30	chr14:104198200-104209000	Strong transcription	Liver	Liver
31	chr14:104198200-104224800	Strong transcription	Left Ventricle	heart
32	chr14:104199400-104204200	Genic enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
33	chr14:104199400-104211800	Strong transcription	Primary T cells fromperipheralblood	blood
34	chr14:104199600-104203800	Weak transcription	Dnd41	blood
35	chr14:104199600-104209000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr14:104199800-104202400	Weak transcription	Fetal Lung	lung
37	chr14:104199800-104205200	Enhancers	Placenta Amnion	Placenta Amnion
38	chr14:104200000-104204400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr14:104200000-104204400	Weak transcription	HSMMtube	muscle
40	chr14:104200000-104220200	Weak transcription	H9 Cell Line	embryonic stem cell
41	chr14:104200200-104204800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
42	chr14:104200200-104209000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
43	chr14:104200200-104214400	Weak transcription	Aorta	Aorta
44	chr14:104200200-104219600	Weak transcription	A549	lung
45	chr14:104200400-104207400	Weak transcription	NH-A	brain
46	chr14:104200400-104210400	Weak transcription	HUES48 Cell Line	embryonic stem cell
47	chr14:104200400-104212800	Weak transcription	Osteobl	bone
48	chr14:104200400-104231800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
49	chr14:104200600-104202400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
50	chr14:104200600-104204200	Genic enhancers	Fetal Adrenal Gland	Adrenal Gland

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