Variant report

Variant	rs1252957
Chromosome Location	chr14:45723014-45723015
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	GATA3	chr14:45722043-45723070	A549	lung:	n/a	n/a
2	IRF4	chr14:45722213-45723097	GM12878	blood:	n/a	n/a
3	EP300	chr14:45722285-45723048	A549	lung:	n/a	n/a
4	CHD2	chr14:45721928-45723221	GM12878	blood:	n/a	chr14:45722220-45722230
5	MAX	chr14:45722024-45723299	A549	lung:	n/a	chr14:45722147-45722154 chr14:45722217-45722227
6	ETS1	chr14:45722179-45723170	A549	lung:	n/a	chr14:45722951-45722964
7	NR3C1	chr14:45722565-45723151	A549	lung:	n/a	chr14:45722894-45722903 chr14:45722896-45722913 chr14:45722895-45722913 chr14:45722891-45722917 chr14:45722896-45722912 chr14:45722891-45722917 chr14:45722897-45722911 chr14:45722895-45722912 chr14:45722891-45722917 chr14:45722891-45722917 chr14:45722896-45722912 chr14:45722896-45722912 chr14:45722897-45722911 chr14:45722891-45722917 chr14:45722893-45722914 chr14:45722897-45722911 chr14:45722896-45722912
8	KAP1	chr14:45722193-45723072	HEK293	kidney:	n/a	n/a
9	FOSL2	chr14:45721989-45723127	A549	lung:	n/a	n/a
10	MAX	chr14:45721967-45723389	HCT-116	colon:	n/a	chr14:45722147-45722154 chr14:45722217-45722227
11	MXI1	chr14:45721668-45723401	IMR90	lung:	n/a	n/a
12	MAX	chr14:45722072-45723267	H1-hESC	embryonic stem cell:	n/a	chr14:45722147-45722154 chr14:45722217-45722227
13	SIN3AK20	chr14:45721828-45723301	MCF-7	breast:	n/a	n/a
14	PAX5	chr14:45722244-45723086	GM12878	blood:	n/a	n/a
15	POLR2A	chr14:45722062-45723616	NB4	blood:	n/a	n/a
16	FOXM1	chr14:45722013-45723160	ECC-1	luminal epithelium:	n/a	n/a
17	CTCF	chr14:45722145-45723135	HCT-116	colon:	n/a	n/a
18	TFAP2C	chr14:45722043-45723148	Hela-S3	cervix:	n/a	chr14:45722319-45722334
19	POLR2A	chr14:45722102-45723597	ECC-1	luminal epithelium:	n/a	n/a
20	POLR2A	chr14:45722109-45723584	PANC-1	pancreas:	n/a	n/a
21	ZNF143	chr14:45722216-45723038	H1-hESC	embryonic stem cell:	n/a	n/a
22	CREB1	chr14:45722186-45723021	ECC-1	luminal epithelium:	n/a	n/a
23	POLR2A	chr14:45722025-45723702	GM12878	blood:	n/a	n/a
24	SIN3AK20	chr14:45721958-45723238	HCT-116	colon:	n/a	n/a
25	POLR2A	chr14:45722116-45723088	PFSK-1	brain:	n/a	n/a
26	USF2	chr14:45722401-45723032	Hela-S3	cervix:	n/a	n/a
27	POLR2A	chr14:45722128-45723021	GM12892	blood:	n/a	n/a
28	CHD2	chr14:45722182-45723522	Hela-S3	cervix:	n/a	chr14:45722220-45722230
29	RUNX3	chr14:45722095-45723159	GM12878	blood:	n/a	n/a
30	POLR2A	chr14:45722149-45723104	HepG2	liver:	n/a	n/a
31	CTCF	chr14:45723007-45723087	MCF-7	breast:	n/a	n/a
32	MAZ	chr14:45722137-45723020	GM12878	blood:	n/a	chr14:45722147-45722154 chr14:45722217-45722227
33	POLR2A	chr14:45721973-45723145	H1-hESC	embryonic stem cell:	n/a	n/a
34	POLR2A	chr14:45721921-45723639	PBDE	blood:	n/a	n/a
35	TEAD4	chr14:45722257-45723080	HepG2	liver:	n/a	n/a
36	CREB1	chr14:45722136-45723359	HepG2	liver:	n/a	n/a
37	ELF1	chr14:45722161-45723024	SK-N-SH	brain:	n/a	chr14:45722409-45722422 chr14:45722214-45722226
38	CTCF	chr14:45722940-45723090	HBMEC	blood vessel:	n/a	n/a
39	POLR2A	chr14:45722096-45723287	HepG2	liver:	n/a	n/a
40	ELK4	chr14:45722123-45723150	Hela-S3	cervix:	n/a	n/a
41	YY1	chr14:45722623-45723117	HepG2	liver:	n/a	chr14:45722876-45722885 chr14:45722874-45722896
42	MYC	chr14:45721755-45723591	NB4	blood:	n/a	chr14:45722147-45722154 chr14:45722217-45722227
43	SETDB1	chr14:45722179-45723106	K562	blood:	n/a	n/a
44	POLR2A	chr14:45722086-45724010	GM12878	blood:	n/a	n/a
45	RCOR1	chr14:45721790-45723568	Hela-S3	cervix:	n/a	n/a
46	SETDB1	chr14:45722278-45723310	U2OS	brain:	n/a	n/a
47	EP300	chr14:45721990-45723018	ECC-1	luminal epithelium:	n/a	n/a
48	NFIC	chr14:45722108-45723043	GM12878	blood:	n/a	n/a
49	MBD4	chr14:45722274-45723111	HepG2	liver:	n/a	n/a
50	MAFK	chr14:45721979-45723553	Hela-S3	cervix:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:45722987-45723037	SAEC	small airway:	n/a
2	chr14:45722987-45723037	GM12878	blood:	n/a
3	chr14:45722987-45723037	K562	blood:	n/a
4	chr14:45722987-45723037	NH-A	brain:	n/a
5	chr14:45722987-45723037	HUVEC	blood vessel:	n/a
6	chr14:45722987-45723037	PANC-1	pancreas:	n/a
7	chr14:45722987-45723037	AoSMC	blood vessel:	n/a
8	chr14:45722987-45723037	SK-N-MC	brain:	n/a
9	chr14:45722987-45723037	HAEpiC	amniotic membrane:	n/a
10	chr14:45722987-45723037	NHBE	bronchial:	n/a
11	chr14:45722987-45723037	HCM	heart:	n/a
12	chr14:45722987-45723037	GM06990	blood:	n/a
13	chr14:45722987-45723037	Hela-S3	cervix:	n/a
14	chr14:45722987-45723037	HRE	kidney:	n/a
15	chr14:45722987-45723037	HCF	heart:	n/a
16	chr14:45722987-45723037	BJ	skin:	n/a
17	chr14:45722987-45723037	HPAEpiC	pulmonary alveolar:	n/a
18	chr14:45722987-45723037	HMEC	breast:	n/a
19	chr14:45722987-45723037	NT2-D1	testis:	n/a
20	chr14:45722987-45723037	HepG2	liver:	n/a
21	chr14:45722987-45723037	SK-N-SH	brain:	n/a
22	chr14:45722987-45723037	GM12891	blood:	n/a
23	chr14:45722987-45723037	SK-N-SH_RA	brain:	n/a
24	chr14:45722987-45723037	Hepatocyte	liver:	n/a
25	chr14:45722987-45723037	HRPEpiC	eye:	n/a
26	chr14:45722987-45723037	HCT-116	colon:	n/a
27	chr14:45722987-45723037	RPTEC	kidney:	n/a
28	chr14:45722987-45723037	LNCaP	prostate:	n/a
29	chr14:45722987-45723037	AG04450	lung:	fetal
30	chr14:45722987-45723037	CMK	blood:	n/a
31	chr14:45722987-45723037	HCPEpiC	choroid plexus:	n/a
32	chr14:45722987-45723037	A549	lung:	n/a
33	chr14:45722987-45723037	HEK293	kidney:	embryo
34	chr14:45722987-45723037	HEEpiC	esophagus:	n/a
35	chr14:45722987-45723037	HRCEpiC	kidney:	n/a
36	chr14:45722987-45723037	MCF-7	breast:	n/a
37	chr14:45722987-45723037	BE2_C	brain:	n/a
38	chr14:45722987-45723037	ECC-1	luminal epithelium:	n/a
39	chr14:45722987-45723037	ovcar-3	ovarian:	n/a
40	chr14:45722987-45723037	T-47D	breast:	n/a
41	chr14:45722987-45723037	AG09319	gingival:	n/a
42	chr14:45722987-45723037	NB4	blood:	n/a
43	chr14:45722987-45723037	U87	brain:	n/a
44	chr14:45722987-45723037	AG04449	skin:	fetal
45	chr14:45722987-45723037	GM12892	blood:	n/a
46	chr14:45722987-45723037	GM19239	blood:	n/a
47	chr14:45722987-45723037	IMR90	lung:	fetal
48	chr14:45722987-45723037	HIPEpiC	eye:	n/a
49	chr14:45722987-45723037	PFSK-1	brain:	n/a
50	chr14:45722987-45723037	HL-60	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr12:57039223..57039923-chr14:45722606..45723303,3	Hela-S3	cervix:
2	chr14:45721810..45725859-chr14:45742099..45745950,4	MCF-7	breast:
3	chr14:45365477..45369212-chr14:45721451..45724440,3	MCF-7	breast:
4	chr14:45602054..45606945-chr14:45719959..45724414,9	MCF-7	breast:
5	chr14:45364937..45368444-chr14:45721075..45725396,9	MCF-7	breast:
6	chr14:45429725..45432587-chr14:45720437..45723992,3	MCF-7	breast:
7	chr14:45722872..45725627-chr6:151936857..151939807,2	MCF-7	breast:
8	chr14:45722471..45723281-chr15:75743983..75744975,2	Hela-S3	cervix:
9	chr14:45588121..45589844-chr14:45722977..45725072,2	MCF-7	breast:
10	chr14:45722854..45723434-chr16:58133168..58133726,2	Hela-S3	cervix:
11	chr14:45601339..45606570-chr14:45722040..45724234,5	MCF-7	breast:

Variant related genes	Relation type
MIS18BP1	TF binding region
MIS18BP1	CpG island
ENSG00000179454	Chromatin interaction
ENSG00000100442	Chromatin interaction
ENSG00000207422	Chromatin interaction
ENSG00000187790	Chromatin interaction
ENSG00000110955	Chromatin interaction
ENSG00000258633	Chromatin interaction
ENSG00000179476	Chromatin interaction
ENSG00000198718	Chromatin interaction
ENSG00000169375	Chromatin interaction
ENSG00000199739	Chromatin interaction

Extended variants
information (count: 57 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:46)

rs_ID	r²[population]
rs10129236	0.83[EUR][1000 genomes]
rs10137415	0.81[EUR][1000 genomes]
rs10142759	0.83[EUR][1000 genomes]
rs10143508	0.83[EUR][1000 genomes]
rs10143794	0.82[AFR][1000 genomes];0.84[AMR][1000 genomes];0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10149578	0.81[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10151937	0.84[EUR][1000 genomes]
rs10220594	0.80[AFR][1000 genomes];0.83[EUR][1000 genomes]
rs11157433	0.83[EUR][1000 genomes]
rs11845507	0.83[EUR][1000 genomes]
rs12433547	0.90[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs12433565	0.88[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1252959	0.95[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1252960	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1252963	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1252966	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1266209	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1268576	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1367580	0.83[EUR][1000 genomes]
rs17115860	0.83[AFR][1000 genomes];0.83[EUR][1000 genomes]
rs17115912	0.93[AFR][1000 genomes];0.88[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17636302	0.86[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2415883	0.82[EUR][1000 genomes]
rs2750119	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28531936	0.89[AFR][1000 genomes];0.84[AMR][1000 genomes];0.98[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs34101857	0.86[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs3825624	0.83[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs3916169	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4900665	0.88[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4900666	0.88[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4900667	0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4906566	0.83[EUR][1000 genomes]
rs4906568	0.83[EUR][1000 genomes]
rs57607457	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs58790242	0.83[EUR][1000 genomes]
rs6572296	0.83[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7141145	0.83[EUR][1000 genomes]
rs7147246	0.86[AFR][1000 genomes];0.84[AMR][1000 genomes];0.98[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7148613	0.83[EUR][1000 genomes]
rs7160373	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73350248	0.87[AFR][1000 genomes];0.84[AMR][1000 genomes];0.98[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs73350255	0.83[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs8010456	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8020533	0.83[EUR][1000 genomes]
rs911040	0.83[EUR][1000 genomes]
rs911041	0.83[AFR][1000 genomes];0.83[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv1803131	chr14:45441932-45726848	Active TSS Weak transcription Enhancers Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
2	nsv901843	chr14:45506857-45833490	Enhancers Strong transcription Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
3	nsv530814	chr14:45604432-46198418	Flanking Active TSS Strong transcription Weak transcription Active TSS Enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
4	nsv901844	chr14:45606287-46063731	Weak transcription Active TSS Strong transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
5	nsv1044445	chr14:45606779-45807171	Transcr. at gene 5' and 3' Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
6	nsv901845	chr14:45619217-45772910	Strong transcription Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
7	nsv1045297	chr14:45631260-45755992	Active TSS Strong transcription Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
8	nsv901846	chr14:45702358-45783546	Enhancers Flanking Active TSS Weak transcription Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
9	nsv564726	chr14:45702358-45911581	Enhancers Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
10	esv2758357	chr14:45706082-45982410	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
11	esv2759987	chr14:45706082-45982410	Active TSS Flanking Active TSS Enhancers Weak transcription Strong transcription Genic enhancers Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:45718800-45723400	Active TSS	Rectal Smooth Muscle	rectum
2	chr14:45718800-45723800	Active TSS	GM12878-XiMat	blood
3	chr14:45719800-45723200	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr14:45720400-45723200	Active TSS	Thymus	Thymus
5	chr14:45720400-45723400	Active TSS	iPS-20b Cell Line	embryonic stem cell
6	chr14:45720400-45723400	Active TSS	HMEC	breast
7	chr14:45720400-45723400	Active TSS	NHLF	lung
8	chr14:45720600-45723400	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
9	chr14:45720600-45723400	Active TSS	Fetal Intestine Large	intestine
10	chr14:45720600-45723600	Active TSS	ES-I3 Cell Line	embryonic stem cell
11	chr14:45720600-45723600	Active TSS	HUES6 Cell Line	embryonic stem cell
12	chr14:45720600-45723600	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
13	chr14:45720600-45723600	Active TSS	Duodenum Smooth Muscle	Duodenum
14	chr14:45720600-45723600	Active TSS	HSMM	muscle
15	chr14:45720600-45723800	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr14:45720800-45723200	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
17	chr14:45720800-45723200	Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
18	chr14:45720800-45723200	Active TSS	NHDF-Ad	bronchial
19	chr14:45720800-45723200	Active TSS	NHEK	skin
20	chr14:45720800-45723400	Active TSS	HUES64 Cell Line	embryonic stem cell
21	chr14:45720800-45723400	Active TSS	iPS-18 Cell Line	embryonic stem cell
22	chr14:45720800-45723400	Active TSS	Fetal Stomach	stomach
23	chr14:45720800-45723600	Active TSS	Brain Angular Gyrus	brain
24	chr14:45720800-45723600	Active TSS	Brain Germinal Matrix	brain
25	chr14:45720800-45723600	Active TSS	Fetal Brain Female	brain
26	chr14:45720800-45723600	Active TSS	Fetal Kidney	kidney
27	chr14:45721000-45723200	Active TSS	Fetal Intestine Small	intestine
28	chr14:45721000-45723400	Active TSS	H9 Cell Line	embryonic stem cell
29	chr14:45721000-45723400	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
30	chr14:45721000-45723400	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
31	chr14:45721000-45723400	Active TSS	Brain Hippocampus Middle	brain
32	chr14:45721000-45723400	Active TSS	Hela-S3	cervix
33	chr14:45721000-45723600	Active TSS	ES-WA7 Cell Line	embryonic stem cell
34	chr14:45721000-45723600	Active TSS	Primary T helper naive cells from peripheral blood	blood
35	chr14:45721000-45723600	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
36	chr14:45721000-45723600	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
37	chr14:45721000-45723600	Active TSS	Brain Anterior Caudate	brain
38	chr14:45721000-45723600	Active TSS	Colonic Mucosa	Colon
39	chr14:45721000-45724000	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
40	chr14:45721200-45723200	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
41	chr14:45721200-45723200	Active TSS	Gastric	stomach
42	chr14:45721200-45723400	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
43	chr14:45721200-45723400	Active TSS	Ovary	ovary
44	chr14:45721200-45723400	Active TSS	Right Ventricle	heart
45	chr14:45721200-45723400	Active TSS	Stomach Smooth Muscle	stomach
46	chr14:45721200-45723600	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
47	chr14:45721200-45723600	Active TSS	Primary T killer memory cells from peripheral blood	blood
48	chr14:45721200-45723600	Active TSS	Psoas Muscle	Psoas
49	chr14:45721200-45723600	Active TSS	HSMMtube	muscle
50	chr14:45721200-45723800	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

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