Variant report

Variant	rs140012242
Chromosome Location	chr4:174090107-174090108
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:234)
CpG islands
(count:61)
Chromatin interactive
region (count:3)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:234 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr4:174089073-174090241	U87	brain:	n/a	n/a
2	MYC	chr4:174089986-174090160	MCF10A-Er-Src	breast:	n/a	n/a
3	IRF1	chr4:174088957-174090113	K562	blood:	n/a	chr4:174089103-174089110 chr4:174089370-174089379 chr4:174089416-174089425 chr4:174089607-174089619 chr4:174089096-174089110
4	POLR2A	chr4:174088947-174090256	PANC-1	pancreas:	n/a	n/a
5	CTCF	chr4:174090020-174090170	SAEC	small airway:	n/a	n/a
6	POLR2A	chr4:174089003-174090139	HUVEC	blood vessel:	n/a	n/a
7	POLR2A	chr4:174088965-174091465	HL-60	blood:	n/a	n/a
8	POLR2A	chr4:174089263-174090214	Hela-S3	cervix:	n/a	n/a
9	MAZ	chr4:174088930-174091911	IMR90	lung:	n/a	chr4:174089336-174089346 chr4:174091392-174091402
10	CTCF	chr4:174090060-174090210	GM12873	blood:	n/a	n/a
11	POLR2A	chr4:174088782-174094458	PANC-1	pancreas:	n/a	n/a
12	TAF1	chr4:174089549-174090149	H1-hESC	embryonic stem cell:	n/a	n/a
13	MAZ	chr4:174089005-174091630	K562	blood:	n/a	chr4:174089336-174089346 chr4:174091392-174091402
14	CTCF	chr4:174090040-174090190	BJ	skin:	n/a	n/a
15	TBL1XR1	chr4:174089995-174090142	K562	blood:	n/a	n/a
16	TBP	chr4:174089052-174090220	K562	blood:	n/a	n/a
17	REST	chr4:174088970-174091683	H1-neurons	neurons:	n/a	chr4:174089347-174089365 chr4:174089565-174089573
18	E2F6	chr4:174090090-174091123	K562	blood:	n/a	chr4:174091060-174091069
19	POLR2A	chr4:174089067-174091578	GM19099	blood:	n/a	n/a
20	POLR2A	chr4:174089018-174091441	K562	blood:	n/a	n/a
21	RELA	chr4:174089051-174091620	GM12891	blood:	n/a	n/a
22	YY1	chr4:174089922-174090406	GM12892	blood:	n/a	n/a
23	CHD2	chr4:174089048-174090124	K562	blood:	n/a	n/a
24	CTCF	chr4:174090020-174090170	HAc	cerebellar:	n/a	n/a
25	TCF12	chr4:174089013-174090407	ECC-1	luminal epithelium:	n/a	n/a
26	POLR2A	chr4:174088863-174091516	GM18526	blood:	n/a	n/a
27	ELF1	chr4:174089042-174091391	GM12878	blood:	n/a	chr4:174091210-174091222 chr4:174091234-174091243 chr4:174089372-174089383
28	POLR2A	chr4:174089275-174091488	ECC-1	luminal epithelium:	n/a	n/a
29	ATF2	chr4:174089161-174090256	GM12878	blood:	n/a	n/a
30	BCLAF1	chr4:174089970-174091477	GM12878	blood:	n/a	chr4:174091074-174091087 chr4:174091188-174091201 chr4:174091390-174091403 chr4:174091058-174091067 chr4:174091053-174091066 chr4:174091339-174091352 chr4:174091237-174091250
31	POLR2A	chr4:174088971-174091378	K562	blood:	n/a	n/a
32	MAX	chr4:174088927-174091694	Hela-S3	cervix:	n/a	chr4:174089336-174089346 chr4:174091392-174091402
33	CTCF	chr4:174090060-174090210	GM12865	blood:	n/a	n/a
34	RAD21	chr4:174089314-174090117	H1-hESC	embryonic stem cell:	n/a	chr4:174089492-174089504
35	TCF7L2	chr4:174089969-174090301	PANC-1	pancreas:	n/a	n/a
36	ZMIZ1	chr4:174089132-174090119	K562	blood:	n/a	n/a
37	CTCF	chr4:174090000-174090150	AG04449	skin:	n/a	n/a
38	EP300	chr4:174089059-174090191	ECC-1	luminal epithelium:	n/a	chr4:174089301-174089315 chr4:174089470-174089479
39	CTCF	chr4:174090060-174090210	SK-N-SH_RA	brain:	n/a	n/a
40	MYC	chr4:174088892-174090213	K562	blood:	n/a	chr4:174089336-174089346
41	POLR2A	chr4:174090068-174090997	A549	lung:	n/a	n/a
42	CTCF	chr4:174090080-174090230	GM12868	blood:	n/a	n/a
43	CTCF	chr4:174089777-174090211	GM12878	blood:	n/a	n/a
44	POLR2A	chr4:174089029-174091518	GM15510	blood:	n/a	n/a
45	POLR2A	chr4:174089127-174090108	SK-N-MC	brain:	n/a	n/a
46	MAX	chr4:174090042-174091513	H1-hESC	embryonic stem cell:	n/a	chr4:174091392-174091402
47	STAT5A	chr4:174089188-174090167	GM12878	blood:	n/a	n/a
48	POLR2A	chr4:174089315-174091391	A549	lung:	n/a	n/a
49	POLR2A	chr4:174090012-174091463	HUVEC	blood vessel:	n/a	n/a
50	POLR2A	chr4:174089174-174090166	SK-N-SH	brain:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:174090085-174090135	AG09319	gingival:	n/a
2	chr4:174090085-174090135	SK-N-SH_RA	brain:	n/a
3	chr4:174090085-174090135	SAEC	small airway:	n/a
4	chr4:174090085-174090135	HUVEC	blood vessel:	n/a
5	chr4:174090085-174090135	HRPEpiC	eye:	n/a
6	chr4:174090085-174090135	AG04449	skin:	fetal
7	chr4:174090085-174090135	NHDF-neo	bronchial:	n/a
8	chr4:174090085-174090135	HL-60	blood:	n/a
9	chr4:174090085-174090135	GM19239	blood:	n/a
10	chr4:174090085-174090135	HNPCEpiC	eye:	n/a
11	chr4:174090085-174090135	GM12878	blood:	n/a
12	chr4:174090085-174090135	HEEpiC	esophagus:	n/a
13	chr4:174090085-174090135	AG04450	lung:	fetal
14	chr4:174090085-174090135	AoSMC	blood vessel:	n/a
15	chr4:174090085-174090135	CMK	blood:	n/a
16	chr4:174090085-174090135	HPAEpiC	pulmonary alveolar:	n/a
17	chr4:174090085-174090135	HCF	heart:	n/a
18	chr4:174090085-174090135	SK-N-MC	brain:	n/a
19	chr4:174090085-174090135	SKMC	muscle:	n/a
20	chr4:174090085-174090135	LNCaP	prostate:	n/a
21	chr4:174090085-174090135	NB4	blood:	n/a
22	chr4:174090085-174090135	Hela-S3	cervix:	n/a
23	chr4:174090085-174090135	GM06990	blood:	n/a
24	chr4:174090085-174090135	RPTEC	kidney:	n/a
25	chr4:174090085-174090135	T-47D	breast:	n/a
26	chr4:174090085-174090135	HRE	kidney:	n/a
27	chr4:174090085-174090135	MCF-7	breast:	n/a
28	chr4:174090085-174090135	GM12891	blood:	n/a
29	chr4:174090085-174090135	HCM	heart:	n/a
30	chr4:174090085-174090135	NH-A	brain:	n/a
31	chr4:174090085-174090135	ProgFib	skin:	n/a
32	chr4:174090085-174090135	H1-hESC	embryonic stem cell:	embryo
33	chr4:174090085-174090135	BE2_C	brain:	n/a
34	chr4:174090085-174090135	PrEC	prostate:	n/a
35	chr4:174090085-174090135	MCF10A-Er-Src	breast:	n/a
36	chr4:174090085-174090135	PFSK-1	brain:	n/a
37	chr4:174090085-174090135	SK-N-SH	brain:	n/a
38	chr4:174090085-174090135	ECC-1	luminal epithelium:	n/a
39	chr4:174090085-174090135	HRCEpiC	kidney:	n/a
40	chr4:174090085-174090135	ovcar-3	ovarian:	n/a
41	chr4:174090085-174090135	NHBE	bronchial:	n/a
42	chr4:174090085-174090135	AG10803	skin:	n/a
43	chr4:174090085-174090135	HAEpiC	amniotic membrane:	n/a
44	chr4:174090085-174090135	Hepatocyte	liver:	n/a
45	chr4:174090085-174090135	HCPEpiC	choroid plexus:	n/a
46	chr4:174090085-174090135	HMEC	breast:	n/a
47	chr4:174090085-174090135	Jurkat	blood:	n/a
48	chr4:174090085-174090135	GM12892	blood:	n/a
49	chr4:174090085-174090135	PANC-1	pancreas:	n/a
50	chr4:174090085-174090135	NT2-D1	testis:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr12:7052640..7053180-chr4:174090042..174090925,2	HCT-116	colon:
2	chr4:174088355..174091772-chr4:174254077..174258410,8	K562	blood:
3	chr4:174088713..174091772-chr4:174254390..174258410,4	K562	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-HMGB2-3	chr4:174090015-174090306	ENSG00000245213
2	lnc-HMGB2-3	chr4:174090015-174090803	ENSG00000245213
3	lnc-HMGB2-3	chr4:174090015-174090337	NONHSAT099223
4	lnc-HMGB2-3	chr4:174090015-174090337	NONHSAT099220

No data

Variant related genes	Relation type
ENSG00000245213	TF binding region
ENSG00000245213	CpG island
ENSG00000238923	Chromatin interaction
ENSG00000111678	Chromatin interaction
ENSG00000164104	Chromatin interaction

Extended variants
information (count: 28 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:28 , 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
11	esv1833960	chr4:174089080-174091110	Active TSS Flanking Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
12	esv3464637	chr4:174089802-174092550	Enhancers Flanking Active TSS Active TSS Genic enhancers Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
13	esv3464638	chr4:174089802-174092550	Active TSS Flanking Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
14	esv1851950	chr4:174090004-174091006	Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
15	esv1840589	chr4:174090004-174091110	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
16	esv1844542	chr4:174090004-174091110	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
17	esv1793244	chr4:174090004-174091120	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
18	esv1799853	chr4:174090004-174091120	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
19	esv1802600	chr4:174090004-174091120	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
20	esv1835664	chr4:174090004-174091120	Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
21	esv1835702	chr4:174090004-174091120	Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
22	esv1841401	chr4:174090004-174091120	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
23	esv1793569	chr4:174090004-174093002	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
24	esv1793960	chr4:174090004-174102397	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
25	esv1801469	chr4:174090004-174102397	Enhancers Active TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
26	esv1799519	chr4:174090004-174173743	Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats Active TSS Genic enhancers Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
27	esv15231	chr4:174090014-174091177	Active TSS Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
28	esv1839763	chr4:174090107-174091110	Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:127 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:174088400-174091400	Active TSS	HUES6 Cell Line	embryonic stem cell
2	chr4:174088400-174091600	Active TSS	HUES48 Cell Line	embryonic stem cell
3	chr4:174088400-174091600	Active TSS	A549	lung
4	chr4:174088400-174092200	Active TSS	H9 Cell Line	embryonic stem cell
5	chr4:174088600-174091400	Active TSS	Rectal Mucosa Donor 31	rectum
6	chr4:174088600-174092000	Active TSS	Rectal Mucosa Donor 29	rectum
7	chr4:174088800-174090200	Active TSS	Fetal Brain Male	brain
8	chr4:174088800-174091400	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr4:174088800-174091400	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr4:174088800-174091400	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
11	chr4:174088800-174091400	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr4:174088800-174091400	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
13	chr4:174088800-174091400	Active TSS	Fetal Intestine Small	intestine
14	chr4:174088800-174091400	Active TSS	Pancreatic Islets	Pancreatic Islet
15	chr4:174088800-174091400	Active TSS	Rectal Smooth Muscle	rectum
16	chr4:174088800-174091600	Active TSS	H1 Cell Line	embryonic stem cell
17	chr4:174088800-174091600	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
18	chr4:174088800-174091600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr4:174088800-174091600	Active TSS	HUES64 Cell Line	embryonic stem cell
20	chr4:174088800-174091600	Active TSS	Brain Inferior Temporal Lobe	brain
21	chr4:174088800-174091600	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
22	chr4:174088800-174091800	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr4:174088800-174091800	Active TSS	Colonic Mucosa	Colon
24	chr4:174088800-174092000	Active TSS	ES-I3 Cell Line	embryonic stem cell
25	chr4:174088800-174092000	Active TSS	Fetal Kidney	kidney
26	chr4:174088800-174092200	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
27	chr4:174088800-174092200	Active TSS	HSMMtube	muscle
28	chr4:174088800-174092400	Active TSS	Thymus	Thymus
29	chr4:174089000-174091200	Active TSS	Fetal Brain Female	brain
30	chr4:174089000-174091400	Active TSS	iPS-15b Cell Line	embryonic stem cell
31	chr4:174089000-174091400	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
32	chr4:174089000-174091400	Active TSS	Brain Hippocampus Middle	brain
33	chr4:174089000-174091400	Active TSS	Colon Smooth Muscle	Colon
34	chr4:174089000-174091400	Active TSS	Fetal Intestine Large	intestine
35	chr4:174089000-174091600	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
36	chr4:174089000-174091600	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
37	chr4:174089000-174091600	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
38	chr4:174089000-174091600	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
39	chr4:174089000-174091600	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
40	chr4:174089000-174091600	Active TSS	Esophagus	oesophagus
41	chr4:174089000-174091600	Active TSS	Gastric	stomach
42	chr4:174089000-174091600	Active TSS	Pancreas	Pancrea
43	chr4:174089000-174091600	Active TSS	Right Ventricle	heart
44	chr4:174089000-174091600	Active TSS	Sigmoid Colon	Sigmoid Colon
45	chr4:174089000-174091600	Active TSS	NHDF-Ad	bronchial
46	chr4:174089000-174091800	Active TSS	ES-WA7 Cell Line	embryonic stem cell
47	chr4:174089000-174091800	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
48	chr4:174089000-174091800	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
49	chr4:174089000-174091800	Active TSS	Psoas Muscle	Psoas
50	chr4:174089000-174092200	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell

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