Variant report

Variant	rs1054497
Chromosome Location	chr4:174089048-174089049
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:111)
CpG islands
(count:61)
Chromatin interactive
region (count:8)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:111 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	IRF1	chr4:174088957-174090113	K562	blood:	n/a	chr4:174089103-174089110 chr4:174089370-174089379 chr4:174089416-174089425 chr4:174089607-174089619 chr4:174089096-174089110
2	POLR2A	chr4:174088947-174090256	PANC-1	pancreas:	n/a	n/a
3	POLR2A	chr4:174089003-174090139	HUVEC	blood vessel:	n/a	n/a
4	POLR2A	chr4:174088965-174091465	HL-60	blood:	n/a	n/a
5	EBF1	chr4:174089004-174089718	GM12878	blood:	n/a	n/a
6	MAZ	chr4:174088930-174091911	IMR90	lung:	n/a	chr4:174089336-174089346 chr4:174091392-174091402
7	POLR2A	chr4:174088782-174094458	PANC-1	pancreas:	n/a	n/a
8	MAZ	chr4:174089005-174091630	K562	blood:	n/a	chr4:174089336-174089346 chr4:174091392-174091402
9	EP300	chr4:174088907-174089476	GM12878	blood:	n/a	chr4:174089301-174089315
10	REST	chr4:174088970-174091683	H1-neurons	neurons:	n/a	chr4:174089347-174089365 chr4:174089565-174089573
11	POLR2A	chr4:174089018-174091441	K562	blood:	n/a	n/a
12	CHD2	chr4:174089048-174090124	K562	blood:	n/a	n/a
13	MAX	chr4:174088996-174089707	MCF-7	breast:	n/a	chr4:174089336-174089346
14	TCF12	chr4:174089013-174090407	ECC-1	luminal epithelium:	n/a	n/a
15	POLR2A	chr4:174088863-174091516	GM18526	blood:	n/a	n/a
16	ELF1	chr4:174089042-174091391	GM12878	blood:	n/a	chr4:174091210-174091222 chr4:174091234-174091243 chr4:174089372-174089383
17	NFIC	chr4:174088972-174089929	GM12878	blood:	n/a	n/a
18	POLR2A	chr4:174088971-174091378	K562	blood:	n/a	n/a
19	MYC	chr4:174089012-174089981	K562	blood:	n/a	chr4:174089336-174089346
20	MAX	chr4:174088927-174091694	Hela-S3	cervix:	n/a	chr4:174089336-174089346 chr4:174091392-174091402
21	MYC	chr4:174089026-174089960	H1-hESC	embryonic stem cell:	n/a	chr4:174089336-174089346
22	TEAD4	chr4:174088863-174090008	K562	blood:	n/a	n/a
23	SMC3	chr4:174088897-174089823	GM12878	blood:	n/a	n/a
24	MYC	chr4:174088892-174090213	K562	blood:	n/a	chr4:174089336-174089346
25	FOXA1	chr4:174089009-174089226	T-47D	breast:	n/a	n/a
26	TCF12	chr4:174088969-174089979	A549	lung:	n/a	n/a
27	POLR2A	chr4:174089029-174091518	GM15510	blood:	n/a	n/a
28	POLR2A	chr4:174088949-174089879	GM12891	blood:	n/a	n/a
29	POLR2A	chr4:174089043-174089223	Hela-S3	cervix:	n/a	n/a
30	ZNF384	chr4:174088741-174089538	GM12878	blood:	n/a	n/a
31	MAX	chr4:174088919-174090283	NB4	blood:	n/a	chr4:174089336-174089346
32	POLR2A	chr4:174089047-174089451	H1-neurons	neurons:	n/a	n/a
33	MYC	chr4:174088917-174091408	K562	blood:	n/a	chr4:174089336-174089346 chr4:174091392-174091402
34	ZBTB7A	chr4:174088940-174091571	ECC-1	luminal epithelium:	n/a	n/a
35	RUNX3	chr4:174088931-174090259	GM12878	blood:	n/a	n/a
36	ARID3A	chr4:174088980-174089588	K562	blood:	n/a	n/a
37	UBTF	chr4:174089026-174091524	K562	blood:	n/a	n/a
38	POLR2A	chr4:174088927-174091471	GM12878	blood:	n/a	n/a
39	POLR2A	chr4:174088995-174091552	GM12892	blood:	n/a	n/a
40	POLR2A	chr4:174088995-174091577	Raji	blood:	n/a	n/a
41	RELA	chr4:174088993-174091622	GM18951	blood:	n/a	n/a
42	MAX	chr4:174088888-174090403	A549	lung:	n/a	chr4:174089336-174089346
43	MXI1	chr4:174088877-174091784	IMR90	lung:	n/a	chr4:174089336-174089345
44	TBP	chr4:174088925-174089527	Hela-S3	cervix:	n/a	n/a
45	MAX	chr4:174089008-174090810	MCF-7	breast:	n/a	chr4:174089336-174089346
46	PML	chr4:174088913-174090209	K562	blood:	n/a	n/a
47	POLR2A	chr4:174089018-174091010	MCF-7	breast:	n/a	n/a
48	POLR2A	chr4:174089012-174091587	GM12878	blood:	n/a	n/a
49	POLR2A	chr4:174089009-174091458	Hela-S3	cervix:	n/a	n/a
50	ELF1	chr4:174089023-174090084	HCT-116	colon:	n/a	chr4:174089372-174089383

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:174089019-174089069	GM12892	blood:	n/a
2	chr4:174089019-174089069	RPTEC	kidney:	n/a
3	chr4:174089019-174089069	HRE	kidney:	n/a
4	chr4:174089019-174089069	NHDF-neo	bronchial:	n/a
5	chr4:174089019-174089069	MCF10A-Er-Src	breast:	n/a
6	chr4:174089019-174089069	AoSMC	blood vessel:	n/a
7	chr4:174089019-174089069	HRPEpiC	eye:	n/a
8	chr4:174089019-174089069	HEK293	kidney:	embryo
9	chr4:174089019-174089069	AG04450	lung:	fetal
10	chr4:174089019-174089069	IMR90	lung:	fetal
11	chr4:174089019-174089069	MCF-7	breast:	n/a
12	chr4:174089019-174089069	AG09319	gingival:	n/a
13	chr4:174089019-174089069	NT2-D1	testis:	n/a
14	chr4:174089019-174089069	NHBE	bronchial:	n/a
15	chr4:174089019-174089069	HCM	heart:	n/a
16	chr4:174089019-174089069	HNPCEpiC	eye:	n/a
17	chr4:174089019-174089069	HRCEpiC	kidney:	n/a
18	chr4:174089019-174089069	GM06990	blood:	n/a
19	chr4:174089019-174089069	HCT-116	colon:	n/a
20	chr4:174089019-174089069	T-47D	breast:	n/a
21	chr4:174089019-174089069	CMK	blood:	n/a
22	chr4:174089019-174089069	NH-A	brain:	n/a
23	chr4:174089019-174089069	HMEC	breast:	n/a
24	chr4:174089019-174089069	BJ	skin:	n/a
25	chr4:174089019-174089069	U87	brain:	n/a
26	chr4:174089019-174089069	H1-hESC	embryonic stem cell:	embryo
27	chr4:174089019-174089069	Jurkat	blood:	n/a
28	chr4:174089019-174089069	PANC-1	pancreas:	n/a
29	chr4:174089019-174089069	AG10803	skin:	n/a
30	chr4:174089019-174089069	Hela-S3	cervix:	n/a
31	chr4:174089019-174089069	A549	lung:	n/a
32	chr4:174089019-174089069	AG04449	skin:	fetal
33	chr4:174089019-174089069	NB4	blood:	n/a
34	chr4:174089019-174089069	HPAEpiC	pulmonary alveolar:	n/a
35	chr4:174089019-174089069	GM12878	blood:	n/a
36	chr4:174089019-174089069	SAEC	small airway:	n/a
37	chr4:174089019-174089069	HUVEC	blood vessel:	n/a
38	chr4:174089019-174089069	HCF	heart:	n/a
39	chr4:174089019-174089069	HCPEpiC	choroid plexus:	n/a
40	chr4:174089019-174089069	GM19239	blood:	n/a
41	chr4:174089019-174089069	SK-N-SH_RA	brain:	n/a
42	chr4:174089019-174089069	PFSK-1	brain:	n/a
43	chr4:174089019-174089069	SKMC	muscle:	n/a
44	chr4:174089019-174089069	SK-N-MC	brain:	n/a
45	chr4:174089019-174089069	PrEC	prostate:	n/a
46	chr4:174089019-174089069	ProgFib	skin:	n/a
47	chr4:174089019-174089069	K562	blood:	n/a
48	chr4:174089019-174089069	Caco-2	colon:	n/a
49	chr4:174089019-174089069	HAEpiC	amniotic membrane:	n/a
50	chr4:174089019-174089069	HEEpiC	esophagus:	n/a

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:174087023..174089565-chr4:174159233..174161373,2	MCF-7	breast:
2	chr4:174080088..174082274-chr4:174088293..174089862,2	MCF-7	breast:
3	chr4:174087322..174089631-chr4:174102847..174104512,2	K562	blood:
4	chr4:174088355..174091772-chr4:174254077..174258410,8	K562	blood:
5	chr4:174072381..174074317-chr4:174086673..174089260,2	K562	blood:
6	chr1:65719996..65720543-chr4:174088718..174089605,2	Hela-S3	cervix:
7	chr4:174088713..174091772-chr4:174254390..174258410,4	K562	blood:
8	chr4:174084331..174086204-chr4:174086936..174089803,3	MCF-7	breast:

No data

Variant related genes	Relation type
GALNT7	TF binding region
GALNT7	CpG island
ENSG00000116675	Chromatin interaction
ENSG00000164104	Chromatin interaction

Extended variants
information (count: 54 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:44)

rs_ID	r²[population]
rs10011724	0.98[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10027708	0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10031414	0.81[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1006002	0.95[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs1006003	0.95[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs1008052	0.85[CHB][hapmap];0.91[CHD][hapmap]
rs1054496	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11737748	0.91[CEU][hapmap];0.80[GIH][hapmap];0.87[TSI][hapmap];0.90[EUR][1000 genomes]
rs12503939	0.85[EUR][1000 genomes]
rs12639929	0.86[CEU][hapmap];0.80[GIH][hapmap];0.82[TSI][hapmap];0.86[EUR][1000 genomes]
rs12644699	0.86[CEU][hapmap];0.80[GIH][hapmap];0.87[TSI][hapmap];0.88[EUR][1000 genomes]
rs13111572	0.86[EUR][1000 genomes]
rs13125240	0.86[CEU][hapmap];0.86[EUR][1000 genomes]
rs13138282	0.90[EUR][1000 genomes]
rs1574314	0.95[CEU][hapmap];0.89[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs17322893	0.91[CEU][hapmap];0.80[GIH][hapmap];0.87[TSI][hapmap];0.90[EUR][1000 genomes]
rs1991727	0.86[CEU][hapmap];0.92[GIH][hapmap];0.94[JPT][hapmap];0.82[TSI][hapmap];0.86[EUR][1000 genomes]
rs2078475	0.96[EUR][1000 genomes]
rs2332654	0.98[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2332655	0.95[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs2332669	0.86[CEU][hapmap];0.94[JPT][hapmap];0.86[EUR][1000 genomes]
rs28477433	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28612521	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28709762	0.89[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2877748	0.95[CEU][hapmap];0.92[GIH][hapmap];0.96[MEX][hapmap];0.95[TSI][hapmap];0.89[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs3733477	0.98[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4377567	0.83[ASW][hapmap];0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.86[MKK][hapmap];1.00[TSI][hapmap];0.90[YRI][hapmap];0.81[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4419455	0.91[CEU][hapmap];0.92[GIH][hapmap];0.87[MEX][hapmap];1.00[TSI][hapmap];0.93[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs4561909	1.00[CEU][hapmap];0.82[GIH][hapmap];0.97[TSI][hapmap];0.99[EUR][1000 genomes]
rs4643788	0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4695826	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs66986541	0.82[AMR][1000 genomes]
rs6814857	1.00[CEU][hapmap];0.91[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs6822683	0.84[ASN][1000 genomes]
rs6822875	0.84[ASN][1000 genomes]
rs6826412	0.85[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs6835098	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6843769	0.84[JPT][hapmap]
rs6851632	0.85[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs7657374	0.83[ASN][1000 genomes]
rs7671278	0.89[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs7672108	0.86[CEU][hapmap];0.92[GIH][hapmap];0.94[JPT][hapmap];0.83[MEX][hapmap];0.80[TSI][hapmap];0.86[EUR][1000 genomes]
rs9990666	0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9997477	0.95[CEU][hapmap];0.85[AMR][1000 genomes];0.94[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3357841	chr4:174088902-174091750	Flanking Active TSS Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
2	esv3403467	chr4:174088977-174092225	Enhancers Active TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
3	esv1798285	chr4:174089048-174091110	Flanking Active TSS Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Weak transcription Enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
4	esv1798967	chr4:174089048-174091110	Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
5	esv1799224	chr4:174089048-174091110	Flanking Active TSS Active TSS Weak transcription Transcr. at gene 5' and 3' Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
6	esv1804824	chr4:174089048-174091110	Active TSS Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
7	esv1810173	chr4:174089048-174091110	Enhancers Flanking Active TSS Active TSS Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
8	esv1834006	chr4:174089048-174091110	Active TSS Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
9	esv1841737	chr4:174089048-174091110	Active TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
10	esv1845734	chr4:174089048-174091110	Active TSS Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:124 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:174073600-174089200	Weak transcription	Aorta	Aorta
2	chr4:174088400-174091400	Active TSS	HUES6 Cell Line	embryonic stem cell
3	chr4:174088400-174091600	Active TSS	HUES48 Cell Line	embryonic stem cell
4	chr4:174088400-174091600	Active TSS	A549	lung
5	chr4:174088400-174092200	Active TSS	H9 Cell Line	embryonic stem cell
6	chr4:174088600-174089400	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
7	chr4:174088600-174089800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr4:174088600-174091400	Active TSS	Rectal Mucosa Donor 31	rectum
9	chr4:174088600-174092000	Active TSS	Rectal Mucosa Donor 29	rectum
10	chr4:174088800-174089200	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
11	chr4:174088800-174089200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
12	chr4:174088800-174089200	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
13	chr4:174088800-174089200	Flanking Active TSS	Muscle Satellite Cultured Cells	--
14	chr4:174088800-174089200	Flanking Active TSS	Brain Anterior Caudate	brain
15	chr4:174088800-174089200	Flanking Active TSS	Duodenum Smooth Muscle	Duodenum
16	chr4:174088800-174089200	Flanking Active TSS	HMEC	breast
17	chr4:174088800-174089200	Flanking Active TSS	K562	blood
18	chr4:174088800-174089400	Flanking Active TSS	Primary T cells from cord blood	blood
19	chr4:174088800-174089400	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
20	chr4:174088800-174089400	Flanking Active TSS	Duodenum Mucosa	Duodenum
21	chr4:174088800-174089600	Flanking Active TSS	Primary B cells from cord blood	blood
22	chr4:174088800-174089600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
23	chr4:174088800-174089600	Flanking Active TSS	Fetal Thymus	thymus
24	chr4:174088800-174089600	Flanking Active TSS	Dnd41	blood
25	chr4:174088800-174089600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
26	chr4:174088800-174089600	Flanking Active TSS	NHEK	skin
27	chr4:174088800-174089800	Flanking Active TSS	Primary hematopoietic stem cells	blood
28	chr4:174088800-174089800	Flanking Active TSS	HUVEC	blood vessel
29	chr4:174088800-174090200	Active TSS	Fetal Brain Male	brain
30	chr4:174088800-174091400	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
31	chr4:174088800-174091400	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr4:174088800-174091400	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
33	chr4:174088800-174091400	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
34	chr4:174088800-174091400	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
35	chr4:174088800-174091400	Active TSS	Fetal Intestine Small	intestine
36	chr4:174088800-174091400	Active TSS	Pancreatic Islets	Pancreatic Islet
37	chr4:174088800-174091400	Active TSS	Rectal Smooth Muscle	rectum
38	chr4:174088800-174091600	Active TSS	H1 Cell Line	embryonic stem cell
39	chr4:174088800-174091600	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
40	chr4:174088800-174091600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr4:174088800-174091600	Active TSS	HUES64 Cell Line	embryonic stem cell
42	chr4:174088800-174091600	Active TSS	Brain Inferior Temporal Lobe	brain
43	chr4:174088800-174091600	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
44	chr4:174088800-174091800	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr4:174088800-174091800	Active TSS	Colonic Mucosa	Colon
46	chr4:174088800-174092000	Active TSS	ES-I3 Cell Line	embryonic stem cell
47	chr4:174088800-174092000	Active TSS	Fetal Kidney	kidney
48	chr4:174088800-174092200	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
49	chr4:174088800-174092200	Active TSS	HSMMtube	muscle
50	chr4:174088800-174092400	Active TSS	Thymus	Thymus

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