Variant report

Variant	rs2295146
Chromosome Location	chr14:104199356-104199357
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr14:104190417..104195099-chr14:104198034..104202895,6	MCF-7	breast:
2	chr14:104199198..104202144-chr14:104204016..104205906,2	K562	blood:
3	chr14:104195134..104197407-chr14:104197892..104201943,5	MCF-7	breast:
4	chr14:104193655..104196381-chr14:104198015..104200284,3	K562	blood:
5	chr14:104178942..104181016-chr14:104198223..104200771,2	K562	blood:

Variant related genes	Relation type
ENSG00000100711	Chromatin interaction
ENSG00000088808	Chromatin interaction
ENSG00000269963	Chromatin interaction
ENSG00000253096	Chromatin interaction
ENSG00000126215	Chromatin interaction

Extended variants
information (count: 89 )
Associated
traits (count: 4 )

rSNPs within LD-proxies of this variant (count:75)

rs_ID	r²[population]
rs1040813	0.85[CEU][hapmap];0.90[CHB][hapmap];0.84[JPT][hapmap]
rs11160758	0.92[AMR][1000 genomes];0.84[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs11160759	0.85[CEU][hapmap];0.95[CHB][hapmap];0.83[JPT][hapmap];0.91[AMR][1000 genomes];0.82[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs11160760	0.85[CEU][hapmap];0.95[CHB][hapmap];0.93[CHD][hapmap];0.88[GIH][hapmap];0.84[JPT][hapmap];0.83[LWK][hapmap];0.91[MEX][hapmap];0.81[TSI][hapmap];0.86[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs11160761	0.86[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs11160762	0.85[CEU][hapmap];0.95[CHB][hapmap];0.93[CHD][hapmap];0.86[GIH][hapmap];0.84[JPT][hapmap];0.85[LWK][hapmap];0.91[MEX][hapmap];0.81[TSI][hapmap];0.86[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs1155751	0.85[CEU][hapmap];0.84[CHB][hapmap]
rs11623546	0.85[CEU][hapmap];0.95[CHB][hapmap];0.93[CHD][hapmap];0.86[GIH][hapmap];0.84[JPT][hapmap];0.83[LWK][hapmap];0.91[MEX][hapmap];0.81[TSI][hapmap];0.82[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs11624184	0.85[CEU][hapmap];0.95[CHB][hapmap];0.82[GIH][hapmap];0.84[JPT][hapmap];0.91[AMR][1000 genomes];0.82[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs11625740	0.81[CEU][hapmap];0.83[CHB][hapmap];0.85[GIH][hapmap];0.86[MEX][hapmap];0.81[TSI][hapmap];0.85[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs11626377	0.84[CEU][hapmap];0.95[CHB][hapmap];0.84[JPT][hapmap];0.91[AMR][1000 genomes];0.82[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs11628240	0.92[AMR][1000 genomes];0.84[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs11628332	0.85[CEU][hapmap];0.95[CHB][hapmap];0.93[CHD][hapmap];0.86[GIH][hapmap];0.84[JPT][hapmap];0.85[LWK][hapmap];0.91[MEX][hapmap];0.81[TSI][hapmap];0.91[AMR][1000 genomes];0.82[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs11628481	0.91[AMR][1000 genomes];0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs11847468	0.85[CEU][hapmap];0.95[CHB][hapmap];0.91[CHD][hapmap];0.86[GIH][hapmap];0.84[JPT][hapmap];0.85[LWK][hapmap];0.91[MEX][hapmap];0.86[TSI][hapmap];0.92[AMR][1000 genomes];0.84[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1187416	0.85[CEU][hapmap];0.90[CHB][hapmap];0.84[JPT][hapmap]
rs12433109	0.96[CEU][hapmap];0.95[CHB][hapmap];0.93[CHD][hapmap];0.97[GIH][hapmap];0.89[JPT][hapmap];0.85[LWK][hapmap];1.00[MEX][hapmap];0.81[MKK][hapmap];0.93[TSI][hapmap];0.92[AMR][1000 genomes];0.91[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs12588489	0.90[AMR][1000 genomes];0.82[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12878682	0.91[AMR][1000 genomes];0.82[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12878868	0.89[AMR][1000 genomes];0.82[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12879501	0.85[CEU][hapmap];0.95[CHB][hapmap];0.93[CHD][hapmap];0.86[GIH][hapmap];0.84[JPT][hapmap];0.85[LWK][hapmap];0.91[MEX][hapmap];0.81[TSI][hapmap];0.82[AMR][1000 genomes]
rs12879612	0.83[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs12880413	0.81[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs12880821	0.84[CEU][hapmap];0.84[CHB][hapmap]
rs12885018	0.85[CEU][hapmap];0.95[CHB][hapmap];0.84[JPT][hapmap];0.82[AMR][1000 genomes]
rs12889993	0.85[CEU][hapmap];0.95[CHB][hapmap];0.93[CHD][hapmap];0.86[GIH][hapmap];0.84[JPT][hapmap];0.83[LWK][hapmap];0.91[MEX][hapmap];0.81[TSI][hapmap];0.82[AMR][1000 genomes]
rs12891175	0.85[CEU][hapmap];0.95[CHB][hapmap];0.93[CHD][hapmap];0.86[GIH][hapmap];0.84[JPT][hapmap];0.85[LWK][hapmap];0.91[MEX][hapmap];0.81[TSI][hapmap];0.81[AMR][1000 genomes]
rs12891589	0.92[AMR][1000 genomes];0.84[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1475007	0.85[CEU][hapmap];0.95[CHB][hapmap];0.95[CHD][hapmap];0.86[GIH][hapmap];0.84[JPT][hapmap];0.85[LWK][hapmap];0.91[MEX][hapmap];0.81[TSI][hapmap]
rs1535097	0.85[CEU][hapmap];0.95[CHB][hapmap];0.93[CHD][hapmap];0.86[GIH][hapmap];0.84[JPT][hapmap];0.85[LWK][hapmap];0.91[MEX][hapmap];0.86[TSI][hapmap];0.92[AMR][1000 genomes];0.84[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1535098	0.84[CEU][hapmap];0.89[CHB][hapmap];0.83[JPT][hapmap];0.92[AMR][1000 genomes];0.84[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1997913	0.81[CEU][hapmap];0.95[CHB][hapmap];0.93[CHD][hapmap];0.85[GIH][hapmap];0.84[JPT][hapmap];0.90[MEX][hapmap];0.86[TSI][hapmap];0.92[AMR][1000 genomes];0.84[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2024667	0.91[AMR][1000 genomes];0.83[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2223937	0.85[CEU][hapmap];0.95[CHB][hapmap];0.95[CHD][hapmap];0.86[GIH][hapmap];0.84[JPT][hapmap];0.91[MEX][hapmap];0.81[TSI][hapmap]
rs2295141	0.85[CEU][hapmap];0.95[CHB][hapmap];0.93[CHD][hapmap];0.86[GIH][hapmap];0.84[JPT][hapmap];0.85[LWK][hapmap];0.91[MEX][hapmap];0.86[TSI][hapmap];0.92[AMR][1000 genomes];0.84[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2295145	0.85[CEU][hapmap];0.81[GIH][hapmap];0.87[LWK][hapmap];0.86[TSI][hapmap];0.86[EUR][1000 genomes]
rs2295147	0.89[CEU][hapmap]
rs2295148	0.89[CEU][hapmap]
rs2295151	0.88[CEU][hapmap]
rs2368560	0.85[CEU][hapmap];0.84[CHB][hapmap]
rs2887282	0.85[CEU][hapmap];0.95[CHB][hapmap];0.95[CHD][hapmap];0.86[GIH][hapmap];0.84[JPT][hapmap];0.85[LWK][hapmap];0.91[MEX][hapmap];0.81[TSI][hapmap]
rs34066659	0.88[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs34813623	0.86[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs35505672	0.86[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs3742365	0.96[CEU][hapmap];0.95[CHB][hapmap];0.89[CHD][hapmap];1.00[GIH][hapmap];0.90[JPT][hapmap];0.89[LWK][hapmap];1.00[MEX][hapmap];0.91[TSI][hapmap];0.82[AFR][1000 genomes];0.98[AMR][1000 genomes];0.93[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs3818085	0.85[CEU][hapmap];0.95[CHB][hapmap];0.93[CHD][hapmap];0.86[GIH][hapmap];0.84[JPT][hapmap];0.85[LWK][hapmap];0.91[MEX][hapmap];0.86[TSI][hapmap];0.92[AMR][1000 genomes];0.84[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs4900594	0.85[CEU][hapmap];0.84[CHB][hapmap];0.82[GIH][hapmap];0.91[MEX][hapmap]
rs4900595	0.86[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs4900600	0.84[CEU][hapmap];0.95[CHB][hapmap];0.84[JPT][hapmap]
rs4906365	0.85[CEU][hapmap];0.83[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs4906371	0.86[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs4906372	0.81[ASN][1000 genomes]
rs4906373	0.82[AMR][1000 genomes]
rs55824307	0.82[AMR][1000 genomes]
rs6575997	0.85[CEU][hapmap];0.95[CHB][hapmap];0.93[CHD][hapmap];0.86[GIH][hapmap];0.84[JPT][hapmap];0.91[MEX][hapmap];0.86[TSI][hapmap];0.91[AMR][1000 genomes];0.83[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs6575999	0.86[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs66509671	0.82[AMR][1000 genomes]
rs67768834	0.92[AMR][1000 genomes];0.84[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7147171	0.85[CEU][hapmap];0.95[CHB][hapmap];0.93[CHD][hapmap];0.86[GIH][hapmap];0.85[LWK][hapmap];0.91[MEX][hapmap];0.81[TSI][hapmap];0.84[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs7149024	0.85[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs7152148	0.91[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs7156697	0.85[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs7156834	0.84[CEU][hapmap];0.83[CHB][hapmap];0.85[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs7159810	0.85[CEU][hapmap];0.95[CHB][hapmap];0.95[CHD][hapmap];0.86[GIH][hapmap];0.84[JPT][hapmap];0.85[LWK][hapmap];0.91[MEX][hapmap];0.81[TSI][hapmap]
rs7401901	0.85[AMR][1000 genomes]
rs8003653	0.85[CEU][hapmap];0.94[CHB][hapmap];0.95[CHD][hapmap];0.86[GIH][hapmap];0.84[JPT][hapmap];0.85[LWK][hapmap];0.91[MEX][hapmap];0.81[TSI][hapmap]
rs8004408	0.85[CEU][hapmap];0.95[CHB][hapmap];0.93[CHD][hapmap];0.88[GIH][hapmap];0.84[JPT][hapmap];0.83[LWK][hapmap];0.91[MEX][hapmap];0.80[MKK][hapmap];0.82[TSI][hapmap];0.94[AMR][1000 genomes];0.82[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs8005225	0.85[CEU][hapmap];0.95[CHB][hapmap];0.95[CHD][hapmap];0.86[GIH][hapmap];0.84[JPT][hapmap];0.85[LWK][hapmap];0.91[MEX][hapmap];0.81[TSI][hapmap]
rs8005594	0.85[CEU][hapmap];0.95[CHB][hapmap];0.84[JPT][hapmap]
rs8009116	0.92[AMR][1000 genomes];0.84[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs8016014	0.84[CEU][hapmap];0.95[CHB][hapmap];0.84[JPT][hapmap]
rs8022783	0.86[AMR][1000 genomes]
rs876002	0.85[CEU][hapmap];0.95[CHB][hapmap];0.93[CHD][hapmap];0.86[GIH][hapmap];0.84[JPT][hapmap];0.85[LWK][hapmap];0.91[MEX][hapmap];0.81[TSI][hapmap];0.91[AMR][1000 genomes];0.82[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs941474	0.85[CEU][hapmap]
rs9743799	0.86[AMR][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:4)

SNP	Gene	Cis/trans	Tissue	Source
rs2295146	KLC1	cis	parietal	SCAN
rs2295146	ZFYVE21	cis	cerebellum	SCAN
rs2295146	C14orf153	cis	parietal	SCAN
rs2295146	RP11-73M18.8	cis	Artery Tibial	GTEx

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:104183400-104200600	Weak transcription	Primary hematopoietic stem cells	blood
2	chr14:104184000-104201200	Weak transcription	HUVEC	blood vessel
3	chr14:104184000-104209000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
4	chr14:104184200-104214400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
5	chr14:104184400-104211000	Weak transcription	Hela-S3	cervix
6	chr14:104189400-104203200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
7	chr14:104190600-104199600	Strong transcription	Dnd41	blood
8	chr14:104190600-104202000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr14:104190800-104204200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr14:104191000-104202000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
11	chr14:104191000-104202200	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
12	chr14:104191000-104203200	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
13	chr14:104191200-104209200	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
14	chr14:104191400-104201400	Strong transcription	Fetal Stomach	stomach
15	chr14:104191400-104201600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr14:104191600-104223800	Weak transcription	Pancreatic Islets	Pancreatic Islet
17	chr14:104191800-104201600	Strong transcription	Primary neutrophils fromperipheralblood	blood
18	chr14:104192000-104201000	Strong transcription	NHLF	lung
19	chr14:104192200-104200400	Strong transcription	HUES48 Cell Line	embryonic stem cell
20	chr14:104192200-104201000	Strong transcription	Primary monocytes fromperipheralblood	blood
21	chr14:104192200-104201600	Strong transcription	Placenta	Placenta
22	chr14:104192200-104216600	Strong transcription	Sigmoid Colon	Sigmoid Colon
23	chr14:104193200-104200000	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
24	chr14:104193400-104201400	Strong transcription	Fetal Muscle Leg	muscle
25	chr14:104194000-104200200	Strong transcription	Aorta	Aorta
26	chr14:104194000-104200400	Strong transcription	iPS DF 6.9 Cell Line	embryonic stem cell
27	chr14:104194000-104201000	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
28	chr14:104194000-104201600	Strong transcription	HUES6 Cell Line	embryonic stem cell
29	chr14:104194000-104209200	Strong transcription	Fetal Intestine Large	intestine
30	chr14:104194200-104201600	Strong transcription	Cortex derived primary cultured neurospheres	brain
31	chr14:104194200-104205600	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
32	chr14:104194200-104211400	Strong transcription	Colonic Mucosa	Colon
33	chr14:104194200-104220400	Strong transcription	Rectal Mucosa Donor 29	rectum
34	chr14:104194400-104208800	Strong transcription	Primary T cells from cord blood	blood
35	chr14:104194600-104206800	Strong transcription	Brain Germinal Matrix	brain
36	chr14:104194800-104201000	Strong transcription	HepG2	liver
37	chr14:104194800-104201400	Strong transcription	Lung	lung
38	chr14:104194800-104209200	Strong transcription	Duodenum Mucosa	Duodenum
39	chr14:104194800-104209200	Strong transcription	Fetal Intestine Small	intestine
40	chr14:104194800-104212000	Strong transcription	Rectal Mucosa Donor 31	rectum
41	chr14:104195000-104200200	Strong transcription	A549	lung
42	chr14:104195000-104201000	Strong transcription	Muscle Satellite Cultured Cells	--
43	chr14:104195200-104200200	Strong transcription	iPS-15b Cell Line	embryonic stem cell
44	chr14:104195200-104200600	Strong transcription	Brain Cingulate Gyrus	brain
45	chr14:104195800-104215200	Weak transcription	HSMM	muscle
46	chr14:104196000-104199400	Weak transcription	Primary B cells from peripheral blood	blood
47	chr14:104196000-104200600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
48	chr14:104196000-104201200	Strong transcription	Brain Anterior Caudate	brain
49	chr14:104196000-104214200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
50	chr14:104196000-104268000	Weak transcription	Small Intestine	intestine

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