Variant report

Variant	rs2332130
Chromosome Location	chr14:24505537-24505538
allele	C/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	POLR2A	chr14:24505477-24506160	ProgFib	skin:	n/a	n/a
2	POLR2A	chr14:24505257-24506313	HUVEC	blood vessel:	n/a	n/a
3	CTCF	chr14:24505387-24506543	A549	lung:	n/a	chr14:24505418-24505431 chr14:24506122-24506140 chr14:24506117-24506138 chr14:24506123-24506139
4	CTCF	chr14:24505521-24505652	MCF-7	breast:	n/a	n/a
5	POLR2A	chr14:24505447-24506241	MCF-7	breast:	n/a	n/a
6	TAF1	chr14:24504822-24506190	HepG2	liver:	n/a	n/a
7	SP1	chr14:24505284-24506348	A549	lung:	n/a	chr14:24505596-24505610 chr14:24506258-24506267 chr14:24506256-24506268 chr14:24505429-24505441 chr14:24506256-24506268 chr14:24506257-24506267 chr14:24505641-24505655 chr14:24505429-24505441 chr14:24505431-24505440 chr14:24505600-24505609 chr14:24505430-24505439 chr14:24506257-24506271
8	POLR2A	chr14:24505450-24506296	PBDE	blood:	n/a	n/a
9	PAX5	chr14:24505440-24505718	GM12892	blood:	n/a	n/a
10	POLR2A	chr14:24505118-24506389	SK-N-MC	brain:	n/a	n/a
11	POLR2A	chr14:24505025-24506196	A549	lung:	n/a	n/a
12	POU2F2	chr14:24504909-24505541	GM12878	blood:	n/a	chr14:24504990-24505004
13	E2F4	chr14:24505473-24505716	MCF10A-Er-Src	breast:	n/a	chr14:24505600-24505612
14	POLR2A	chr14:24505224-24506200	H1-hESC	embryonic stem cell:	n/a	n/a
15	POLR2A	chr14:24505403-24506184	H1-hESC	embryonic stem cell:	n/a	n/a
16	RAD21	chr14:24505397-24506308	HepG2	liver:	n/a	chr14:24506038-24506052 chr14:24506120-24506139 chr14:24505419-24505432 chr14:24505428-24505438
17	POLR2A	chr14:24504890-24506185	HepG2	liver:	n/a	n/a
18	POLR2A	chr14:24505369-24505810	H1-hESC	embryonic stem cell:	n/a	n/a
19	POLR2A	chr14:24505478-24505820	HL-60	blood:	n/a	n/a
20	CTCF	chr14:24505520-24505670	GM12873	blood:	n/a	n/a
21	CTCF	chr14:24505520-24505670	BJ	skin:	n/a	n/a
22	JUND	chr14:24504937-24506264	HepG2	liver:	n/a	chr14:24505835-24505843
23	CEBPD	chr14:24505308-24505800	HepG2	liver:	n/a	n/a
24	PBX3	chr14:24505431-24505701	GM12878	blood:	n/a	n/a
25	POLR2A	chr14:24505200-24506263	HepG2	liver:	n/a	n/a
26	MAX	chr14:24505528-24505820	ECC-1	luminal epithelium:	n/a	n/a
27	JUND	chr14:24505519-24505632	H1-hESC	embryonic stem cell:	n/a	n/a
28	POLR2A	chr14:24505320-24506319	GM12892	blood:	n/a	n/a
29	POLR2A	chr14:24504987-24506333	GM12892	blood:	n/a	n/a
30	SIN3A	chr14:24505496-24506252	H1-hESC	embryonic stem cell:	n/a	chr14:24505968-24505977 chr14:24505970-24505979
31	POLR2A	chr14:24505422-24505683	PANC-1	pancreas:	n/a	n/a
32	POLR2A	chr14:24505309-24506179	A549	lung:	n/a	n/a
33	MAZ	chr14:24505421-24506251	Hela-S3	cervix:	n/a	chr14:24505967-24505980 chr14:24505969-24505978 chr14:24505968-24505979 chr14:24505967-24505980 chr14:24505969-24505979 chr14:24505968-24505979 chr14:24505968-24505979 chr14:24505968-24505978 chr14:24505970-24505979 chr14:24505967-24505980 chr14:24505964-24505983 chr14:24505968-24505978 chr14:24505969-24505979 chr14:24505968-24505979 chr14:24505969-24505978 chr14:24505969-24505978
34	TAF1	chr14:24505299-24505751	H1-hESC	embryonic stem cell:	n/a	n/a
35	POLR2A	chr14:24505375-24506278	ECC-1	luminal epithelium:	n/a	n/a
36	POLR2A	chr14:24505357-24506225	Hela-S3	cervix:	n/a	n/a
37	SP1	chr14:24504070-24506291	HepG2	liver:	n/a	chr14:24505596-24505610 chr14:24506258-24506267 chr14:24505023-24505037 chr14:24506256-24506268 chr14:24505429-24505441 chr14:24506256-24506268 chr14:24506257-24506267 chr14:24505641-24505655 chr14:24505132-24505146 chr14:24505429-24505441 chr14:24505431-24505440 chr14:24505600-24505609 chr14:24505430-24505439 chr14:24506257-24506271
38	POLR2A	chr14:24505381-24506179	GM18951	blood:	n/a	n/a
39	USF1	chr14:24505377-24505697	HepG2	liver:	n/a	n/a
40	TCF12	chr14:24505432-24505715	GM12878	blood:	n/a	chr14:24505591-24505598
41	TCF12	chr14:24505270-24506442	A549	lung:	n/a	chr14:24505591-24505598
42	CTCF	chr14:24505521-24505548	GM19238	blood:	n/a	n/a
43	TCF12	chr14:24505366-24505743	GM12878	blood:	n/a	chr14:24505591-24505598
44	CTCF	chr14:24505420-24505570	SAEC	small airway:	n/a	n/a
45	HA-E2F1	chr14:24505341-24506036	Hela-S3	cervix:	n/a	chr14:24505600-24505612 chr14:24505939-24505946
46	POLR2A	chr14:24505457-24506300	SK-N-SH	brain:	n/a	n/a
47	MAX	chr14:24505450-24505844	A549	lung:	n/a	n/a
48	E2F1	chr14:24505378-24505779	Hela-S3	cervix:	n/a	chr14:24505600-24505612
49	CTCF	chr14:24505487-24505626	GM10266	blood:	n/a	n/a
50	CEBPB	chr14:24505530-24505585	Hela-S3	cervix:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:24505537-24505587	SKMC	muscle:	n/a
2	chr14:24505537-24505587	ECC-1	luminal epithelium:	n/a
3	chr14:24505537-24505587	Hepatocyte	liver:	n/a
4	chr14:24505537-24505587	GM12892	blood:	n/a
5	chr14:24505537-24505587	BE2_C	brain:	n/a
6	chr14:24505537-24505587	BJ	skin:	n/a
7	chr14:24505537-24505587	SK-N-SH_RA	brain:	n/a
8	chr14:24505537-24505587	HCF	heart:	n/a
9	chr14:24505537-24505587	PFSK-1	brain:	n/a
10	chr14:24505537-24505587	CMK	blood:	n/a
11	chr14:24505537-24505587	IMR90	lung:	fetal
12	chr14:24505537-24505587	SK-N-MC	brain:	n/a
13	chr14:24505537-24505587	Hela-S3	cervix:	n/a
14	chr14:24505537-24505587	T-47D	breast:	n/a
15	chr14:24505537-24505587	H1-hESC	embryonic stem cell:	embryo
16	chr14:24505537-24505587	HIPEpiC	eye:	n/a
17	chr14:24505537-24505587	LNCaP	prostate:	n/a
18	chr14:24505537-24505587	GM12891	blood:	n/a
19	chr14:24505537-24505587	NHDF-neo	bronchial:	n/a
20	chr14:24505537-24505587	Jurkat	blood:	n/a
21	chr14:24505537-24505587	HEK293	kidney:	embryo
22	chr14:24505537-24505587	K562	blood:	n/a
23	chr14:24505537-24505587	MCF-7	breast:	n/a
24	chr14:24505537-24505587	AG10803	skin:	n/a
25	chr14:24505537-24505587	Caco-2	colon:	n/a
26	chr14:24505537-24505587	GM12878	blood:	n/a
27	chr14:24505537-24505587	HCT-116	colon:	n/a
28	chr14:24505537-24505587	HUVEC	blood vessel:	n/a
29	chr14:24505537-24505587	AoSMC	blood vessel:	n/a
30	chr14:24505537-24505587	HepG2	liver:	n/a
31	chr14:24505537-24505587	HCPEpiC	choroid plexus:	n/a
32	chr14:24505537-24505587	AG04449	skin:	fetal
33	chr14:24505537-24505587	PANC-1	pancreas:	n/a
34	chr14:24505537-24505587	PrEC	prostate:	n/a
35	chr14:24505537-24505587	AG09319	gingival:	n/a
36	chr14:24505537-24505587	MCF10A-Er-Src	breast:	n/a
37	chr14:24505537-24505587	AG04450	lung:	fetal
38	chr14:24505537-24505587	GM06990	blood:	n/a
39	chr14:24505537-24505587	HEEpiC	esophagus:	n/a
40	chr14:24505537-24505587	NT2-D1	testis:	n/a
41	chr14:24505537-24505587	ovcar-3	ovarian:	n/a
42	chr14:24505537-24505587	NH-A	brain:	n/a
43	chr14:24505537-24505587	HNPCEpiC	eye:	n/a
44	chr14:24505537-24505587	HPAEpiC	pulmonary alveolar:	n/a
45	chr14:24505537-24505587	NB4	blood:	n/a
46	chr14:24505537-24505587	HCM	heart:	n/a
47	chr14:24505537-24505587	HMEC	breast:	n/a
48	chr14:24505537-24505587	GM19239	blood:	n/a
49	chr14:24505537-24505587	HRE	kidney:	n/a
50	chr14:24505537-24505587	NHBE	bronchial:	n/a

No.	Distal block	Cell Line	Cell type
1	chr14:24504090..24505966-chr14:24768791..24770568,2	MCF-7	breast:
2	chr14:24503791..24508058-chr14:24562194..24566408,5	MCF-7	breast:
3	chr14:24505124..24506975-chr14:24520204..24522367,2	MCF-7	breast:
4	chr14:24504490..24506127-chr14:24583788..24585514,2	MCF-7	breast:
5	chr14:24505359..24507247-chr14:24702110..24704400,2	MCF-7	breast:
6	chr14:24422701..24424551-chr14:24504249..24506129,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000225766	TF binding region
ENSG00000225766	CpG island
ENSG00000100938	Chromatin interaction
ENSG00000157379	Chromatin interaction
ENSG00000129535	Chromatin interaction
ENSG00000215256	Chromatin interaction
ENSG00000196943	Chromatin interaction
ENSG00000157326	Chromatin interaction
ENSG00000100889	Chromatin interaction
ENSG00000186648	Chromatin interaction
ENSG00000100897	Chromatin interaction

Extended variants
information (count: 33 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs12588225	0.93[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs12589203	0.93[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12590397	0.91[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1811890	0.82[EUR][1000 genomes]
rs2006084	0.93[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2277477	0.91[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2277478	0.87[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs4981492	0.89[ASN][1000 genomes]
rs4982826	0.82[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:24 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3405661	chr14:24189883-24670942	Strong transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	131 gene(s)	inside rSNPs	diseases
2	nsv1217	chr14:24400565-24512689	Active TSS Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
3	nsv1049316	chr14:24405420-24583724	Enhancers Active TSS Bivalent Enhancer Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	72 gene(s)	inside rSNPs	diseases
4	nsv541999	chr14:24405420-24583724	Enhancers Active TSS Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	72 gene(s)	inside rSNPs	diseases
5	esv2761633	chr14:24423582-24513917	Flanking Active TSS Enhancers Weak transcription Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
6	nsv564047	chr14:24428509-24525634	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
7	nsv901497	chr14:24429249-24514449	Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
8	nsv1052180	chr14:24429298-24555710	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
9	nsv826901	chr14:24457315-24508468	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
10	nsv1048292	chr14:24474511-24513905	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	11 gene(s)	inside rSNPs	diseases
11	nsv9126	chr14:24475840-24505714	Weak transcription Active TSS Enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	11 gene(s)	inside rSNPs	diseases
12	nsv1049192	chr14:24478882-24519250	Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	13 gene(s)	inside rSNPs	diseases
13	nsv1037929	chr14:24478882-24522447	Bivalent Enhancer Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region	15 gene(s)	inside rSNPs	diseases
14	nsv1052857	chr14:24479375-24513905	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	11 gene(s)	inside rSNPs	diseases
15	nsv1047042	chr14:24484459-24513905	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	10 gene(s)	inside rSNPs	diseases
16	nsv1038839	chr14:24488131-24510197	Enhancers Active TSS Flanking Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	10 gene(s)	inside rSNPs	diseases
17	nsv1044763	chr14:24488131-24513905	Active TSS Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	10 gene(s)	inside rSNPs	diseases
18	nsv1051893	chr14:24488131-24519250	Flanking Active TSS Active TSS Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	12 gene(s)	inside rSNPs	diseases
19	nsv1043854	chr14:24488131-24522447	Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Enhancers Bivalent/Poised TSS Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	14 gene(s)	inside rSNPs	diseases
20	nsv1049849	chr14:24488384-24513905	Flanking Active TSS Enhancers Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	10 gene(s)	inside rSNPs	diseases
21	nsv516023	chr14:24489605-24550224	Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
22	nsv1038278	chr14:24494063-24513905	Flanking Active TSS Enhancers Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	10 gene(s)	inside rSNPs	diseases
23	nsv1042507	chr14:24494153-24513905	Weak transcription Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	10 gene(s)	inside rSNPs	diseases
24	nsv983808	chr14:24503854-24523979	Weak transcription Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	15 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:121 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:24503600-24505600	Weak transcription	NHLF	lung
2	chr14:24503800-24505600	Weak transcription	NHDF-Ad	bronchial
3	chr14:24505000-24505600	Active TSS	Primary hematopoietic stem cells	blood
4	chr14:24505000-24505600	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr14:24505000-24506200	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr14:24505000-24506200	Active TSS	HUES6 Cell Line	embryonic stem cell
7	chr14:24505000-24506200	Active TSS	iPS-18 Cell Line	embryonic stem cell
8	chr14:24505000-24506200	Active TSS	Brain Anterior Caudate	brain
9	chr14:24505000-24506200	Active TSS	Stomach Smooth Muscle	stomach
10	chr14:24505000-24506200	Active TSS	A549	lung
11	chr14:24505000-24506400	Active TSS	HUES64 Cell Line	embryonic stem cell
12	chr14:24505000-24506600	Flanking Active TSS	Dnd41	blood
13	chr14:24505200-24505600	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
14	chr14:24505200-24505600	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
15	chr14:24505200-24505600	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
16	chr14:24505200-24505600	Active TSS	Primary mononuclear cells fromperipheralblood	Blood
17	chr14:24505200-24505600	Active TSS	Skeletal Muscle Male	skeletal muscle
18	chr14:24505200-24505600	Active TSS	Skeletal Muscle Female	skeletal muscle
19	chr14:24505200-24505600	Enhancers	Stomach Mucosa	stomach
20	chr14:24505200-24505600	Active TSS	HepG2	liver
21	chr14:24505200-24505800	Active TSS	Primary T helper cells fromperipheralblood	blood
22	chr14:24505200-24505800	Active TSS	Fetal Lung	lung
23	chr14:24505200-24505800	Active TSS	Fetal Stomach	stomach
24	chr14:24505200-24505800	Flanking Active TSS	Fetal Thymus	thymus
25	chr14:24505200-24506000	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
26	chr14:24505200-24506000	Active TSS	Fetal Brain Female	brain
27	chr14:24505200-24506000	Active TSS	GM12878-XiMat	blood
28	chr14:24505200-24506200	Active TSS	H1 Cell Line	embryonic stem cell
29	chr14:24505200-24506200	Active TSS	H9 Cell Line	embryonic stem cell
30	chr14:24505200-24506200	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr14:24505200-24506200	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
32	chr14:24505200-24506200	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
33	chr14:24505200-24506200	Active TSS	iPS-15b Cell Line	embryonic stem cell
34	chr14:24505200-24506200	Active TSS	iPS-20b Cell Line	embryonic stem cell
35	chr14:24505200-24506200	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
36	chr14:24505200-24506200	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
37	chr14:24505200-24506200	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
38	chr14:24505200-24506200	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
39	chr14:24505200-24506200	Flanking Active TSS	Primary T cells fromperipheralblood	blood
40	chr14:24505200-24506200	Active TSS	Primary T helper cells PMA-I stimulated	--
41	chr14:24505200-24506200	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
42	chr14:24505200-24506200	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
43	chr14:24505200-24506200	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
44	chr14:24505200-24506200	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
45	chr14:24505200-24506200	Active TSS	Brain Cingulate Gyrus	brain
46	chr14:24505200-24506200	Active TSS	Brain Hippocampus Middle	brain
47	chr14:24505200-24506200	Active TSS	Brain Inferior Temporal Lobe	brain
48	chr14:24505200-24506200	Active TSS	Colon Smooth Muscle	Colon
49	chr14:24505200-24506200	Active TSS	Duodenum Mucosa	Duodenum
50	chr14:24505200-24506200	Active TSS	Fetal Heart	heart

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