Variant report

Variant	rs4092293
Chromosome Location	chr5:43018651-43018652
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:18)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:18 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:43015093..43022227-chr5:43063428..43069370,31	MCF-7	breast:
2	chr5:40796840..40798415-chr5:43016929..43019400,2	MCF-7	breast:
3	chr16:89988917..89989811-chr5:43018161..43019027,2	Hela-S3	cervix:
4	chr19:13049374..13049937-chr5:43017996..43018694,2	NB4	blood:
5	chr5:43014739..43026335-chr5:43034830..43045515,33	MCF-7	breast:
6	chr16:31191270..31191892-chr5:43018071..43018743,2	Hela-S3	cervix:
7	chr5:43016691..43021968-chr5:43036071..43044426,17	MCF-7	breast:
8	chr1:57110974..57111787-chr5:43018020..43018793,2	Hela-S3	cervix:
9	chr15:59664817..59665719-chr5:43017980..43018660,2	Hela-S3	cervix:
10	chr5:43017018..43021813-chr5:43064660..43069370,12	MCF-7	breast:
11	chr12:6643784..6644570-chr5:43017791..43018727,2	Hela-S3	cervix:
12	chr5:43015314..43020034-chr5:43032196..43035172,5	MCF-7	breast:
13	chr17:36858634..36859302-chr5:43018121..43018959,2	Hela-S3	cervix:
14	chr5:43017490..43020535-chr5:43119535..43122363,3	MCF-7	breast:
15	chr12:104359505..104360344-chr5:43018121..43018755,2	Hela-S3	cervix:
16	chr13:111365120..111365861-chr5:43018102..43019042,2	Hela-S3	cervix:
17	chr11:65625774..65626580-chr5:43018226..43018829,2	Hela-S3	cervix:
18	chr5:43018130..43019042-chr6:31795467..31796002,2	Hela-S3	cervix:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF131-2	chr5:43018531-43018774	ENSG00000251131.1
2	lnc-ZNF131-2	chr5:43018585-43018774	ENSG00000251131.1

No data

Variant related genes	Relation type
ENSG00000215068	Chromatin interaction
ENSG00000261005	Chromatin interaction
ENSG00000259006	Chromatin interaction
ENSG00000089280	Chromatin interaction
ENSG00000111640	Chromatin interaction
ENSG00000177721	Chromatin interaction
ENSG00000258947	Chromatin interaction
ENSG00000172757	Chromatin interaction
ENSG00000162409	Chromatin interaction
ENSG00000179218	Chromatin interaction
ENSG00000172262	Chromatin interaction
ENSG00000157470	Chromatin interaction
ENSG00000157483	Chromatin interaction
ENSG00000162407	Chromatin interaction
ENSG00000272382	Chromatin interaction
ENSG00000139372	Chromatin interaction
ENSG00000204388	Chromatin interaction
ENSG00000177738	Chromatin interaction
ENSG00000153487	Chromatin interaction
ENSG00000132356	Chromatin interaction

Extended variants
information (count: 107 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:94)

rs_ID	r²[population]
rs10064003	0.96[CEU][hapmap];0.82[CHB][hapmap];0.95[JPT][hapmap];0.91[AMR][1000 genomes];0.90[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs10522	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.88[AFR][1000 genomes];0.97[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10941604	0.95[JPT][hapmap];0.89[ASN][1000 genomes]
rs10941605	0.81[CHB][hapmap];0.95[JPT][hapmap];0.89[ASN][1000 genomes]
rs11747435	0.89[ASN][1000 genomes]
rs11747714	0.88[CHD][hapmap];0.95[JPT][hapmap]
rs11958008	0.89[ASN][1000 genomes]
rs12697439	0.92[CEU][hapmap];0.94[CHB][hapmap];1.00[JPT][hapmap];0.86[YRI][hapmap];0.94[AFR][1000 genomes];0.98[AMR][1000 genomes];0.91[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs13169690	0.83[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.82[LWK][hapmap];1.00[MEX][hapmap];0.96[MKK][hapmap];0.94[TSI][hapmap];0.82[YRI][hapmap];0.87[AFR][1000 genomes];0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs13170208	0.94[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs13171133	0.86[ASN][1000 genomes]
rs13178479	0.95[ASN][1000 genomes]
rs13179934	0.89[AMR][1000 genomes];0.87[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1542369	0.94[CHB][hapmap];0.97[CHD][hapmap];1.00[JPT][hapmap];0.80[MEX][hapmap];0.95[ASN][1000 genomes]
rs1574407	1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[ASN][1000 genomes]
rs160709	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.97[TSI][hapmap];0.99[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1618891	0.84[CHD][hapmap];0.90[JPT][hapmap]
rs1624415	0.84[CHD][hapmap];0.90[JPT][hapmap]
rs178415	1.00[CHB][hapmap];0.92[CHD][hapmap];1.00[JPT][hapmap]
rs186323	0.80[ASN][1000 genomes]
rs186324	0.83[CHB][hapmap];0.95[JPT][hapmap];0.89[AMR][1000 genomes]
rs1902101	0.89[AMR][1000 genomes];0.86[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2100473	1.00[CEU][hapmap];0.81[CHB][hapmap];0.95[JPT][hapmap];0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2124069	0.82[AFR][1000 genomes];0.88[AMR][1000 genomes];0.87[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs222060	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.97[TSI][hapmap];0.99[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2247280	0.88[AMR][1000 genomes]
rs2253450	0.89[ASN][1000 genomes]
rs2329994	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2329995	1.00[ASW][hapmap];0.92[CEU][hapmap];0.94[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.87[LWK][hapmap];1.00[MEX][hapmap];0.96[MKK][hapmap];0.89[TSI][hapmap];0.86[YRI][hapmap];0.92[AFR][1000 genomes];0.98[AMR][1000 genomes];0.91[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2548334	0.83[CHB][hapmap];0.88[CHD][hapmap];0.93[GIH][hapmap];0.95[JPT][hapmap];1.00[MEX][hapmap];0.89[AMR][1000 genomes]
rs2548339	0.80[ASN][1000 genomes]
rs2548345	0.89[AMR][1000 genomes];0.90[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2548349	0.87[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs2548350	0.95[CEU][hapmap];0.87[CHB][hapmap];0.90[JPT][hapmap];0.88[AMR][1000 genomes];0.88[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2548353	0.88[CEU][hapmap];0.95[JPT][hapmap];0.90[AMR][1000 genomes];0.89[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2548356	0.88[CEU][hapmap];0.95[JPT][hapmap];0.91[AMR][1000 genomes];0.88[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2548373	0.89[AMR][1000 genomes]
rs2603295	0.82[ASN][1000 genomes]
rs2603620	0.89[AMR][1000 genomes];0.90[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs2603634	0.89[AMR][1000 genomes]
rs2603636	0.82[ASN][1000 genomes]
rs2603644	0.95[JPT][hapmap]
rs2603656	0.83[CHB][hapmap];0.97[CHD][hapmap];0.95[JPT][hapmap];0.80[MEX][hapmap];0.89[ASN][1000 genomes]
rs2882295	0.95[JPT][hapmap]
rs2924817	0.86[AMR][1000 genomes]
rs309909	0.96[CEU][hapmap];0.83[CHB][hapmap];0.92[CHD][hapmap];0.85[GIH][hapmap];0.95[JPT][hapmap];1.00[MEX][hapmap];0.83[TSI][hapmap];0.87[AMR][1000 genomes];0.90[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs309914	0.96[CEU][hapmap];0.94[CHB][hapmap];1.00[JPT][hapmap];0.97[AMR][1000 genomes];0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs309921	0.84[AMR][1000 genomes]
rs309923	0.89[CHD][hapmap];0.95[GIH][hapmap];0.95[JPT][hapmap];0.84[MEX][hapmap];0.80[ASN][1000 genomes]
rs309924	0.81[CHB][hapmap];0.95[JPT][hapmap];0.88[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs309925	0.82[CHB][hapmap];0.95[JPT][hapmap];0.84[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs309926	0.83[CHB][hapmap];0.95[JPT][hapmap];0.89[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs309927	0.83[CHB][hapmap];0.95[JPT][hapmap];0.89[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs309948	0.89[AMR][1000 genomes]
rs309950	0.88[CHD][hapmap];0.95[JPT][hapmap]
rs309951	0.83[ASN][1000 genomes]
rs316395	0.89[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs316396	0.90[ASN][1000 genomes]
rs316400	0.87[ASN][1000 genomes]
rs316402	0.82[ASN][1000 genomes]
rs316403	0.82[ASN][1000 genomes]
rs316404	1.00[CHB][hapmap];0.95[CHD][hapmap];1.00[JPT][hapmap];0.85[ASN][1000 genomes]
rs316408	1.00[CHB][hapmap];0.95[CHD][hapmap];1.00[JPT][hapmap];0.85[ASN][1000 genomes]
rs316413	1.00[CHB][hapmap];0.92[CHD][hapmap];1.00[JPT][hapmap]
rs316414	0.88[CEU][hapmap];0.94[CHB][hapmap];0.97[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.89[TSI][hapmap];0.96[AMR][1000 genomes];0.91[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs316416	0.96[AMR][1000 genomes];0.91[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs316419	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs316422	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs3909456	0.90[CHD][hapmap];0.95[JPT][hapmap]
rs4033115	0.85[AFR][1000 genomes];0.97[AMR][1000 genomes];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4092294	0.83[ASW][hapmap];0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.85[LWK][hapmap];0.96[MEX][hapmap];0.92[MKK][hapmap];1.00[TSI][hapmap];0.96[YRI][hapmap];0.89[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4296812	0.93[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs512921	0.90[JPT][hapmap]
rs515970	0.87[ASN][1000 genomes]
rs543569	0.87[ASN][1000 genomes]
rs557076	0.84[CHD][hapmap];0.90[JPT][hapmap]
rs565761	0.87[ASN][1000 genomes]
rs567884	0.84[CHD][hapmap];0.90[JPT][hapmap]
rs613825	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs643307	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6451660	0.96[CEU][hapmap];0.94[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.86[AFR][1000 genomes];0.97[AMR][1000 genomes];0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6451661	0.96[CEU][hapmap];0.94[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];0.98[AMR][1000 genomes];0.91[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6451662	0.83[ASW][hapmap];0.92[CEU][hapmap];0.94[CHB][hapmap];0.97[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.82[LWK][hapmap];1.00[MEX][hapmap];0.96[MKK][hapmap];0.89[TSI][hapmap];0.96[YRI][hapmap];0.86[AFR][1000 genomes];0.97[AMR][1000 genomes];0.91[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6875214	0.80[AFR][1000 genomes];0.95[AMR][1000 genomes];0.88[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6879130	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[YRI][hapmap]
rs6892422	0.84[CHD][hapmap];0.90[JPT][hapmap]
rs724430	0.94[CHB][hapmap];0.95[JPT][hapmap];0.95[ASN][1000 genomes]
rs768441	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7715065	0.95[JPT][hapmap];0.90[ASN][1000 genomes]
rs782971	0.90[JPT][hapmap]
rs782978	0.84[CHD][hapmap];0.90[JPT][hapmap]
rs782984	0.84[CHD][hapmap];0.90[JPT][hapmap]
rs903391	0.90[JPT][hapmap]
rs9292862	1.00[CEU][hapmap];1.00[CHB][hapmap];0.97[CHD][hapmap];0.98[GIH][hapmap];1.00[JPT][hapmap];0.92[MEX][hapmap];0.97[TSI][hapmap];0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:13 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv993554	chr5:42720939-43251863	Bivalent/Poised TSS Strong transcription Active TSS Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	298 gene(s)	inside rSNPs	diseases
2	nsv462126	chr5:42728831-43237188	Active TSS Enhancers Bivalent Enhancer Weak transcription Genic enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	297 gene(s)	inside rSNPs	diseases
3	nsv597925	chr5:42728831-43237188	Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription Bivalent Enhancer Strong transcription Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	297 gene(s)	inside rSNPs	diseases
4	nsv1023741	chr5:42768215-43348145	Flanking Active TSS Weak transcription Bivalent/Poised TSS Enhancers Strong transcription Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	309 gene(s)	inside rSNPs	diseases
5	nsv537737	chr5:42768215-43348145	Genic enhancers Enhancers Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	309 gene(s)	inside rSNPs	diseases
6	nsv534185	chr5:42804840-43067088	Weak transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	165 gene(s)	inside rSNPs	diseases
7	nsv1029288	chr5:42928085-43047323	Flanking Bivalent TSS/Enh Active TSS Genic enhancers Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	120 gene(s)	inside rSNPs	diseases
8	nsv968169	chr5:42956713-43043472	Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	116 gene(s)	inside rSNPs	diseases
9	nsv1024636	chr5:42959979-43295782	Active TSS Bivalent Enhancer Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	283 gene(s)	inside rSNPs	diseases
10	nsv537739	chr5:42959979-43295782	Strong transcription Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	283 gene(s)	inside rSNPs	diseases
11	nsv880447	chr5:42967215-43030798	Bivalent Enhancer Active TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	97 gene(s)	inside rSNPs	diseases
12	nsv881640	chr5:42978644-43028221	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Weak transcription Enhancers ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	94 gene(s)	inside rSNPs	diseases
13	nsv880415	chr5:42978644-43030798	Flanking Active TSS Enhancers Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	94 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs4092293	PPP2R2A	trans	parietal	SCAN

Chromatin state (count:115 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:43016400-43020800	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr5:43016800-43020800	Bivalent/Poised TSS	Rectal Smooth Muscle	rectum
3	chr5:43017200-43018800	Flanking Bivalent TSS/Enh	Fetal Muscle Leg	muscle
4	chr5:43017200-43019200	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
5	chr5:43017200-43019200	Active TSS	HSMM	muscle
6	chr5:43017200-43019400	Bivalent/Poised TSS	Small Intestine	intestine
7	chr5:43017200-43020200	Bivalent/Poised TSS	Colon Smooth Muscle	Colon
8	chr5:43017200-43020600	Bivalent/Poised TSS	Brain Dorsolateral Prefrontal Cortex	brain
9	chr5:43017200-43020800	Bivalent/Poised TSS	Duodenum Smooth Muscle	Duodenum
10	chr5:43017400-43018800	Bivalent/Poised TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr5:43017400-43018800	Bivalent/Poised TSS	Breast Myoepithelial Primary Cells	Breast
12	chr5:43017400-43018800	Flanking Bivalent TSS/Enh	Fetal Adrenal Gland	Adrenal Gland
13	chr5:43017400-43019000	Active TSS	Esophagus	oesophagus
14	chr5:43017400-43019200	Bivalent/Poised TSS	H9 Cell Line	embryonic stem cell
15	chr5:43017400-43019200	Bivalent/Poised TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
16	chr5:43017400-43019200	Active TSS	Aorta	Aorta
17	chr5:43017400-43019400	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr5:43017400-43019600	Active TSS	Sigmoid Colon	Sigmoid Colon
19	chr5:43017400-43019800	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
20	chr5:43017400-43020000	Active TSS	Right Atrium	heart
21	chr5:43017400-43020200	Bivalent/Poised TSS	Brain Cingulate Gyrus	brain
22	chr5:43017400-43020400	Active TSS	Primary T helper memory cells from peripheral blood 2	blood
23	chr5:43017400-43020400	Active TSS	Dnd41	blood
24	chr5:43017400-43020600	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
25	chr5:43017400-43020600	Active TSS	Primary T helper cells PMA-I stimulated	--
26	chr5:43017400-43020600	Active TSS	Primary T killer memory cells from peripheral blood	blood
27	chr5:43017400-43020600	Bivalent/Poised TSS	Left Ventricle	heart
28	chr5:43017400-43020600	Bivalent/Poised TSS	Psoas Muscle	Psoas
29	chr5:43017400-43020600	Active TSS	Right Ventricle	heart
30	chr5:43017400-43020600	Active TSS	Thymus	Thymus
31	chr5:43017400-43020600	Active TSS	HSMMtube	muscle
32	chr5:43017400-43021400	Active TSS	A549	lung
33	chr5:43017600-43018800	Flanking Bivalent TSS/Enh	Cortex derived primary cultured neurospheres	brain
34	chr5:43017600-43018800	Flanking Bivalent TSS/Enh	Fetal Stomach	stomach
35	chr5:43017600-43019000	Active TSS	ES-I3 Cell Line	embryonic stem cell
36	chr5:43017600-43019000	Active TSS	NHEK	skin
37	chr5:43017600-43019400	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
38	chr5:43017600-43019600	Active TSS	NHDF-Ad	bronchial
39	chr5:43017600-43019800	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
40	chr5:43017600-43019800	Active TSS	NHLF	lung
41	chr5:43017600-43020200	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
42	chr5:43017600-43020200	Bivalent/Poised TSS	Fetal Kidney	kidney
43	chr5:43017600-43020400	Active TSS	Primary monocytes fromperipheralblood	blood
44	chr5:43017600-43020400	Bivalent/Poised TSS	Brain Inferior Temporal Lobe	brain
45	chr5:43017600-43020400	Active TSS	Monocytes-CD14+_RO01746	blood
46	chr5:43017600-43020600	Active TSS	Primary B cells from peripheral blood	blood
47	chr5:43017600-43020600	Active TSS	Primary T cells from cord blood	blood
48	chr5:43017600-43020600	Active TSS	Primary T cells fromperipheralblood	blood
49	chr5:43017600-43020600	Active TSS	Primary T helper naive cells from peripheral blood	blood
50	chr5:43017600-43020600	Active TSS	Primary T helper memory cells from peripheral blood 1	blood

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