Variant report

Variant	rs2603656
Chromosome Location	chr5:42992040-42992041
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:19)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:19 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:42879448..42882053-chr5:42991985..42994094,2	K562	blood:
2	chr5:42991555..42992778-chr5:43020174..43020852,3	Hela-S3	cervix:
3	chr19:11199685..11200284-chr5:42991786..42992687,2	NB4	blood:
4	chr5:42990996..42996897-chr5:43036694..43045949,13	K562	blood:
5	chr19:47759450..47760347-chr5:42991556..42992526,2	NB4	blood:
6	chr5:42991975..42992808-chr5:43007900..43008580,2	NB4	blood:
7	chr5:42974190..42975842-chr5:42991638..42994075,2	MCF-7	breast:
8	chr5:42991772..42994897-chr5:42997978..43001031,3	MCF-7	breast:
9	chr1:92952332..92952877-chr5:42991579..42992543,2	NB4	blood:
10	chr5:42988028..42998045-chr5:43036469..43045844,20	K562	blood:
11	chr5:42989723..42997135-chr5:43060250..43070296,19	K562	blood:
12	chr5:42992038..42994724-chr5:43120190..43122287,2	K562	blood:
13	chr5:42990973..42999044-chr5:43062393..43068169,17	K562	blood:
14	chr5:42989588..43001279-chr5:43004636..43014428,32	K562	blood:
15	chr5:42989969..42995303-chr5:43120044..43124152,6	K562	blood:
16	chr5:41924886..41927114-chr5:42991951..42994899,2	K562	blood:
17	chr5:42991959..42992680-chr5:43019227..43019905,2	Hela-S3	cervix:
18	chr5:42942640..42945683-chr5:42991617..42995259,4	K562	blood:
19	chr5:42941021..42945683-chr5:42991872..42995259,5	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C5orf39-2	chr5:42991255-42992726	XLOC_004803

No data

Variant related genes	Relation type
ENSG00000105321	Chromatin interaction
ENSG00000162676	Chromatin interaction
ENSG00000151876	Chromatin interaction
ENSG00000272144	Chromatin interaction
ENSG00000177738	Chromatin interaction
ENSG00000172262	Chromatin interaction
ENSG00000271788	Chromatin interaction
ENSG00000130164	Chromatin interaction
ENSG00000215068	Chromatin interaction
ENSG00000177721	Chromatin interaction

Extended variants
information (count: 103 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:86)

rs_ID	r²[population]
rs10064003	0.81[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10522	0.81[CEU][hapmap];0.83[CHB][hapmap];0.95[JPT][hapmap];0.82[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10941604	1.00[CEU][hapmap];0.94[CHB][hapmap];1.00[JPT][hapmap];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10941605	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11747435	0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11747714	0.94[CHB][hapmap];0.90[CHD][hapmap];1.00[JPT][hapmap]
rs11958008	0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12697439	0.89[CHB][hapmap];0.95[JPT][hapmap];0.83[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs13169690	0.83[CHB][hapmap];0.97[CHD][hapmap];0.95[JPT][hapmap];0.80[MEX][hapmap];0.81[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs13170208	1.00[CEU][hapmap];0.89[CHB][hapmap];0.95[JPT][hapmap];0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs13171133	0.84[ASN][1000 genomes]
rs13178479	0.88[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs13179934	0.90[ASN][1000 genomes]
rs1542369	1.00[CEU][hapmap];0.89[CHB][hapmap];1.00[CHD][hapmap];0.95[GIH][hapmap];0.95[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1574407	0.89[CHB][hapmap];0.95[JPT][hapmap]
rs160709	0.83[CHB][hapmap];0.97[CHD][hapmap];0.95[JPT][hapmap];0.80[MEX][hapmap];0.80[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1618891	0.82[CHD][hapmap];0.86[JPT][hapmap]
rs1624415	0.82[CHD][hapmap];0.86[JPT][hapmap]
rs178415	0.83[CHB][hapmap];0.89[CHD][hapmap];0.95[JPT][hapmap]
rs186323	0.86[ASN][1000 genomes]
rs186324	1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[ASN][1000 genomes]
rs1902101	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2100473	1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2124069	0.90[ASN][1000 genomes]
rs222060	0.83[CHB][hapmap];0.97[CHD][hapmap];0.95[JPT][hapmap];0.80[MEX][hapmap];0.80[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2253450	0.91[CEU][hapmap];0.87[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2329994	0.87[ASN][1000 genomes]
rs2329995	0.89[CHB][hapmap];0.97[CHD][hapmap];0.95[JPT][hapmap];0.80[MEX][hapmap];0.83[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2548334	1.00[CHB][hapmap];0.90[CHD][hapmap];1.00[JPT][hapmap];0.82[ASN][1000 genomes]
rs2548336	0.88[CHB][hapmap]
rs2548339	0.86[ASN][1000 genomes]
rs2548341	0.83[ASN][1000 genomes]
rs2548343	0.84[ASN][1000 genomes]
rs2548345	0.85[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2548346	0.85[ASN][1000 genomes]
rs2548349	0.82[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2548350	0.83[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.83[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2548353	0.88[CEU][hapmap];0.94[CHB][hapmap];1.00[JPT][hapmap];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2548356	0.88[CEU][hapmap];0.94[CHB][hapmap];1.00[JPT][hapmap];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2603620	0.85[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2603644	0.94[CHB][hapmap];1.00[JPT][hapmap];0.82[ASN][1000 genomes]
rs2882295	0.94[CHB][hapmap];1.00[JPT][hapmap];0.83[ASN][1000 genomes]
rs309909	0.81[CEU][hapmap];1.00[CHB][hapmap];0.95[CHD][hapmap];1.00[JPT][hapmap];0.80[MEX][hapmap];0.85[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs309914	0.81[CEU][hapmap];0.89[CHB][hapmap];0.95[JPT][hapmap];0.84[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs309922	0.83[ASN][1000 genomes]
rs309923	0.94[CHB][hapmap];0.92[CHD][hapmap];1.00[JPT][hapmap];0.86[ASN][1000 genomes]
rs309924	1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[ASN][1000 genomes]
rs309925	1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[ASN][1000 genomes]
rs309926	1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[ASN][1000 genomes]
rs309927	1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[ASN][1000 genomes]
rs309948	0.82[ASN][1000 genomes]
rs309950	0.94[CHB][hapmap];0.90[CHD][hapmap];1.00[JPT][hapmap]
rs316395	0.87[ASN][1000 genomes]
rs316396	0.81[ASN][1000 genomes]
rs316404	0.83[CHB][hapmap];0.92[CHD][hapmap];0.95[JPT][hapmap]
rs316408	0.83[CHB][hapmap];0.92[CHD][hapmap];0.95[JPT][hapmap]
rs316413	0.83[CHB][hapmap];0.89[CHD][hapmap];0.95[JPT][hapmap]
rs316414	0.88[CEU][hapmap];0.89[CHB][hapmap];1.00[CHD][hapmap];0.95[JPT][hapmap];0.80[MEX][hapmap];0.85[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs316416	0.85[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs316419	0.87[ASN][1000 genomes]
rs316422	0.87[ASN][1000 genomes]
rs3909456	0.89[CHB][hapmap];0.92[CHD][hapmap];1.00[JPT][hapmap];0.81[ASN][1000 genomes]
rs4033115	0.82[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4092293	0.83[CHB][hapmap];0.97[CHD][hapmap];0.95[JPT][hapmap];0.80[MEX][hapmap];0.89[ASN][1000 genomes]
rs4092294	0.83[CHB][hapmap];0.97[CHD][hapmap];0.95[JPT][hapmap];0.89[ASN][1000 genomes]
rs4296812	0.84[ASN][1000 genomes]
rs512921	0.86[JPT][hapmap]
rs557076	0.82[CHD][hapmap];0.86[JPT][hapmap]
rs567884	0.82[CHD][hapmap];0.86[JPT][hapmap]
rs613825	0.87[ASN][1000 genomes]
rs643307	0.83[CHB][hapmap];0.95[JPT][hapmap];0.89[ASN][1000 genomes]
rs6451660	0.81[CEU][hapmap];0.89[CHB][hapmap];0.95[JPT][hapmap];0.84[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6451661	0.81[CEU][hapmap];0.89[CHB][hapmap];0.95[JPT][hapmap];0.83[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6451662	0.89[CHB][hapmap];1.00[CHD][hapmap];0.95[JPT][hapmap];0.80[MEX][hapmap];0.83[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6875214	0.80[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs6879130	0.83[CHB][hapmap];0.95[JPT][hapmap]
rs6890469	0.82[CHD][hapmap]
rs6892422	0.81[CHD][hapmap];0.86[JPT][hapmap]
rs724430	1.00[CEU][hapmap];0.89[CHB][hapmap];0.90[JPT][hapmap];0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs768441	0.83[CHB][hapmap];0.95[JPT][hapmap];0.80[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7715065	1.00[CEU][hapmap];0.84[CHB][hapmap];1.00[JPT][hapmap];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs782971	0.86[JPT][hapmap]
rs782978	0.82[CHD][hapmap];0.86[JPT][hapmap]
rs782984	0.82[CHD][hapmap];0.86[JPT][hapmap]
rs903391	0.86[JPT][hapmap]
rs9292862	0.83[CHB][hapmap];0.95[CHD][hapmap];0.95[JPT][hapmap];0.87[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:17 , 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	esv1813779	chr5:42906572-42992040	Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
8	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
9	nsv1020910	chr5:42929799-43000021	Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	38 gene(s)	inside rSNPs	diseases
10	nsv537738	chr5:42929799-43000021	Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Enhancers Genic enhancers Bivalent/Poised TSS Weak transcription Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	38 gene(s)	inside rSNPs	diseases
11	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
12	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
13	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
14	nsv881436	chr5:42967215-43008917	Flanking Active TSS Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	50 gene(s)	inside rSNPs	diseases
15	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
16	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
17	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

No data

Chromatin state (count:117 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:42987200-42992400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr5:42988400-42996200	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr5:42989400-42992600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr5:42990200-42992600	Bivalent/Poised TSS	Duodenum Smooth Muscle	Duodenum
5	chr5:42990200-42996000	Flanking Active TSS	Primary mononuclear cells fromperipheralblood	Blood
6	chr5:42990600-42992600	Flanking Active TSS	K562	blood
7	chr5:42990800-42992200	Bivalent/Poised TSS	Colonic Mucosa	Colon
8	chr5:42990800-42992200	Active TSS	Small Intestine	intestine
9	chr5:42990800-42992400	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
10	chr5:42990800-42992400	Flanking Active TSS	Hela-S3	cervix
11	chr5:42990800-42992600	Flanking Active TSS	Primary hematopoietic stem cells	blood
12	chr5:42990800-42993400	Bivalent/Poised TSS	Brain Substantia Nigra	brain
13	chr5:42990800-42993800	Active TSS	Sigmoid Colon	Sigmoid Colon
14	chr5:42990800-42996000	Bivalent/Poised TSS	Rectal Smooth Muscle	rectum
15	chr5:42991000-42992200	Flanking Active TSS	Adipose Nuclei	Adipose
16	chr5:42991000-42995600	Active TSS	Right Ventricle	heart
17	chr5:42991200-42992200	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
18	chr5:42991200-42992200	Bivalent/Poised TSS	Stomach Smooth Muscle	stomach
19	chr5:42991200-42995400	Active TSS	NHLF	lung
20	chr5:42991200-42995800	Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
21	chr5:42991200-42995800	Active TSS	Thymus	Thymus
22	chr5:42991400-42992200	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
23	chr5:42991400-42992200	Bivalent/Poised TSS	Liver	Liver
24	chr5:42991400-42992200	Bivalent/Poised TSS	Brain Inferior Temporal Lobe	brain
25	chr5:42991400-42992200	Bivalent/Poised TSS	Esophagus	oesophagus
26	chr5:42991400-42992400	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin01	Skin
27	chr5:42991400-42992400	Flanking Active TSS	Placenta	Placenta
28	chr5:42991400-42992600	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
29	chr5:42991400-42992800	ZNF genes & repeats	Lung	lung
30	chr5:42991400-42993000	Bivalent/Poised TSS	iPS DF 6.9 Cell Line	embryonic stem cell
31	chr5:42991400-42993200	Bivalent/Poised TSS	Pancreatic Islets	Pancreatic Islet
32	chr5:42991400-42994600	Bivalent/Poised TSS	Left Ventricle	heart
33	chr5:42991400-42995400	Bivalent/Poised TSS	Brain Cingulate Gyrus	brain
34	chr5:42991400-42995400	Bivalent/Poised TSS	Brain Hippocampus Middle	brain
35	chr5:42991400-42995600	Active TSS	Primary T helper memory cells from peripheral blood 2	blood
36	chr5:42991400-42995800	Active TSS	Primary T helper naive cells from peripheral blood	blood
37	chr5:42991400-42995800	Bivalent/Poised TSS	Duodenum Mucosa	Duodenum
38	chr5:42991600-42992200	Active TSS	Primary T helper 17 cells PMA-I stimulated	--
39	chr5:42991600-42992400	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
40	chr5:42991600-42992600	Flanking Bivalent TSS/Enh	H1 Cell Line	embryonic stem cell
41	chr5:42991600-42992600	Bivalent/Poised TSS	Psoas Muscle	Psoas
42	chr5:42991600-42993200	Bivalent/Poised TSS	H9 Cell Line	embryonic stem cell
43	chr5:42991600-42993200	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
44	chr5:42991600-42993400	Flanking Bivalent TSS/Enh	Fetal Muscle Trunk	muscle
45	chr5:42991600-42993400	Flanking Bivalent TSS/Enh	Fetal Muscle Leg	muscle
46	chr5:42991600-42993400	Active TSS	Spleen	Spleen
47	chr5:42991600-42993600	Flanking Bivalent TSS/Enh	Fetal Adrenal Gland	Adrenal Gland
48	chr5:42991600-42993800	Active TSS	Primary T cells from cord blood	blood
49	chr5:42991600-42993800	Active TSS	Primary T helper memory cells from peripheral blood 1	blood
50	chr5:42991600-42994800	Bivalent/Poised TSS	Brain Dorsolateral Prefrontal Cortex	brain

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