Variant report

Variant	esv3317310
Chromosome Location	chr18:14450493-14460678
allele	n/a
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	CEBPB	chr18:14458091-14458453	HepG2	liver:	n/a	n/a
2	CTCF	chr18:14455520-14455670	MCF-7	breast:	n/a	n/a
3	CTCF	chr18:14458660-14458810	HUVEC	blood vessel:	n/a	chr18:14458737-14458753 chr18:14458736-14458754 chr18:14458743-14458750
4	CTCF	chr18:14458650-14458828	SK-N-SH_RA	brain:	n/a	chr18:14458737-14458753 chr18:14458736-14458754 chr18:14458743-14458750
5	CTCF	chr18:14459920-14460070	WERI-Rb-1	eye:	n/a	chr18:14459995-14460013 chr18:14459998-14460011
6	CTCF	chr18:14458080-14458230	GM12873	blood:	n/a	chr18:14458126-14458139
7	CTCF	chr18:14458001-14458168	LNCaP	prostate:	n/a	chr18:14458126-14458139
8	CTCF	chr18:14458668-14458856	K562	blood:	n/a	chr18:14458737-14458753 chr18:14458736-14458754 chr18:14458834-14458847 chr18:14458743-14458750
9	CTCF	chr18:14459856-14460140	LNCaP	prostate:	n/a	chr18:14459995-14460013 chr18:14459998-14460011
10	CTCF	chr18:14458380-14458530	GM12869	blood:	n/a	n/a
11	CTCF	chr18:14458652-14458818	Gliobla	brain:	n/a	chr18:14458737-14458753 chr18:14458736-14458754 chr18:14458743-14458750
12	CTCF	chr18:14458680-14458830	HepG2	liver:	n/a	chr18:14458737-14458753 chr18:14458736-14458754 chr18:14458743-14458750
13	CTCF	chr18:14458616-14458889	Pancreas_OC	pancreas:	n/a	chr18:14458737-14458753 chr18:14458736-14458754 chr18:14458834-14458847 chr18:14458743-14458750
14	CTCF	chr18:14458486-14458977	K562	blood:	n/a	chr18:14458737-14458753 chr18:14458736-14458754 chr18:14458834-14458847 chr18:14458743-14458750
15	CTCF	chr18:14458078-14458124	Spleen_OC	spleen:	n/a	n/a
16	CTCF	chr18:14458680-14458830	GM12875	blood:	n/a	chr18:14458737-14458753 chr18:14458736-14458754 chr18:14458743-14458750
17	CTCF	chr18:14458629-14458864	MCF-7	breast:	n/a	chr18:14458737-14458753 chr18:14458736-14458754 chr18:14458834-14458847 chr18:14458743-14458750
18	CTCF	chr18:14458820-14458970	A549	lung:	n/a	chr18:14458834-14458847
19	CTCF	chr18:14458800-14458950	GM12866	blood:	n/a	chr18:14458834-14458847
20	CTCF	chr18:14458660-14458810	GM12878	blood:	n/a	chr18:14458737-14458753 chr18:14458736-14458754 chr18:14458743-14458750
21	CTCF	chr18:14458618-14458795	HepG2	liver:	n/a	chr18:14458737-14458753 chr18:14458736-14458754 chr18:14458743-14458750
22	CTCF	chr18:14458627-14458860	ProgFib	skin:	n/a	chr18:14458737-14458753 chr18:14458736-14458754 chr18:14458834-14458847 chr18:14458743-14458750
23	CTCF	chr18:14458560-14458710	HCT-116	colon:	n/a	n/a
24	CTCF	chr18:14459911-14460071	MCF-7	breast:	n/a	chr18:14459995-14460013 chr18:14459998-14460011
25	CTCF	chr18:14458054-14458161	GM12891	blood:	n/a	chr18:14458126-14458139
26	CTCF	chr18:14458614-14458858	MCF-7	breast:	n/a	chr18:14458737-14458753 chr18:14458736-14458754 chr18:14458834-14458847 chr18:14458743-14458750
27	CTCF	chr18:14458664-14458812	Hela-S3	cervix:	n/a	chr18:14458737-14458753 chr18:14458736-14458754 chr18:14458743-14458750
28	CTCF	chr18:14459914-14460044	SK-N-SH_RA	brain:	n/a	chr18:14459995-14460013 chr18:14459998-14460011
29	CTCF	chr18:14458583-14459020	SK-N-SH	brain:	n/a	chr18:14458737-14458753 chr18:14458736-14458754 chr18:14458834-14458847 chr18:14458743-14458750
30	CTCF	chr18:14458531-14458943	A549	lung:	n/a	chr18:14458737-14458753 chr18:14458736-14458754 chr18:14458834-14458847 chr18:14458743-14458750
31	CTCF	chr18:14458160-14458310	GM06990	blood:	n/a	n/a
32	CTCF	chr18:14450535-14450639	A549	lung:	n/a	n/a
33	CTCF	chr18:14458080-14458230	HepG2	liver:	n/a	chr18:14458126-14458139
34	CTCF	chr18:14458614-14458868	Lung_OC	lung:	n/a	chr18:14458737-14458753 chr18:14458736-14458754 chr18:14458834-14458847 chr18:14458743-14458750
35	CTCF	chr18:14458680-14458830	HRPEpiC	eye:	n/a	chr18:14458737-14458753 chr18:14458736-14458754 chr18:14458743-14458750
36	CTCF	chr18:14458056-14458161	GM19238	blood:	n/a	chr18:14458126-14458139
37	CTCF	chr18:14458600-14458750	HRPEpiC	eye:	n/a	chr18:14458743-14458750
38	CTCF	chr18:14458700-14458850	AG04449	skin:	n/a	chr18:14458737-14458753 chr18:14458736-14458754 chr18:14458834-14458847 chr18:14458743-14458750
39	CTCF	chr18:14457980-14458130	GM12875	blood:	n/a	n/a
40	CTCF	chr18:14458560-14458945	GM19238	blood:	n/a	chr18:14458737-14458753 chr18:14458736-14458754 chr18:14458834-14458847 chr18:14458743-14458750
41	CTCF	chr18:14458580-14458730	HFF	foreskin:	n/a	n/a
42	CTCF	chr18:14459840-14459990	BE2_C	brain:	n/a	n/a
43	CTCF	chr18:14458612-14458871	MCF-7	breast:	n/a	chr18:14458737-14458753 chr18:14458736-14458754 chr18:14458834-14458847 chr18:14458743-14458750
44	CTCF	chr18:14458600-14458750	HCM	heart:	n/a	chr18:14458743-14458750
45	CTCF	chr18:14458656-14458847	GM19240	blood:	n/a	chr18:14458737-14458753 chr18:14458736-14458754 chr18:14458834-14458847 chr18:14458743-14458750
46	CTCF	chr18:14458598-14458912	A549	lung:	n/a	chr18:14458737-14458753 chr18:14458736-14458754 chr18:14458834-14458847 chr18:14458743-14458750
47	CTCF	chr18:14458958-14459015	GM19238	blood:	n/a	n/a
48	CTCF	chr18:14458600-14458750	GM12867	blood:	n/a	chr18:14458743-14458750
49	CTCF	chr18:14458560-14458710	MCF-7	breast:	n/a	n/a
50	CTCF	chr18:14458625-14458872	GM10248	blood:	n/a	chr18:14458737-14458753 chr18:14458736-14458754 chr18:14458834-14458847 chr18:14458743-14458750

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr18:14458692-14458742	ovcar-3	ovarian:	n/a
2	chr18:14458692-14458742	ovcar-3	ovarian:	n/a
3	chr18:14458161-14458211	Hela-S3	cervix:	n/a
4	chr18:14450799-14450849	AG10803	skin:	n/a
5	chr18:14457820-14457870	HRCEpiC	kidney:	n/a
6	chr18:14457820-14457870	Hepatocyte	liver:	n/a
7	chr18:14451035-14451085	PFSK-1	brain:	n/a
8	chr18:14457820-14457870	HEEpiC	esophagus:	n/a
9	chr18:14458161-14458211	ECC-1	luminal epithelium:	n/a
10	chr18:14458692-14458742	ECC-1	luminal epithelium:	n/a
11	chr18:14458692-14458742	NH-A	brain:	n/a
12	chr18:14451035-14451085	HRPEpiC	eye:	n/a
13	chr18:14451035-14451085	AoSMC	blood vessel:	n/a
14	chr18:14450799-14450849	HAEpiC	amniotic membrane:	n/a
15	chr18:14458161-14458211	NHDF-neo	bronchial:	n/a
16	chr18:14459174-14459224	GM12891	blood:	n/a
17	chr18:14455307-14455357	HMEC	breast:	n/a
18	chr18:14450799-14450849	GM06990	blood:	n/a
19	chr18:14459044-14459094	GM06990	blood:	n/a
20	chr18:14457820-14457870	H1-hESC	embryonic stem cell:	embryo
21	chr18:14458161-14458211	PrEC	prostate:	n/a
22	chr18:14457820-14457870	GM12891	blood:	n/a
23	chr18:14450799-14450849	HCM	heart:	n/a
24	chr18:14459174-14459224	H1-hESC	embryonic stem cell:	embryo
25	chr18:14459174-14459224	RPTEC	kidney:	n/a
26	chr18:14458692-14458742	NHDF-neo	bronchial:	n/a
27	chr18:14459044-14459094	HEEpiC	esophagus:	n/a
28	chr18:14458692-14458742	AG09309	skin:	n/a
29	chr18:14459044-14459094	HCM	heart:	n/a
30	chr18:14458692-14458742	HRPEpiC	eye:	n/a
31	chr18:14457820-14457870	T-47D	breast:	n/a
32	chr18:14459174-14459224	NT2-D1	testis:	n/a
33	chr18:14459044-14459094	PANC-1	pancreas:	n/a
34	chr18:14458927-14458977	HL-60	blood:	n/a
35	chr18:14450799-14450849	SKMC	muscle:	n/a
36	chr18:14458161-14458211	HCM	heart:	n/a
37	chr18:14459044-14459094	GM19239	blood:	n/a
38	chr18:14450799-14450849	Caco-2	colon:	n/a
39	chr18:14458927-14458977	HAEpiC	amniotic membrane:	n/a
40	chr18:14458927-14458977	Hela-S3	cervix:	n/a
41	chr18:14458927-14458977	GM12891	blood:	n/a
42	chr18:14457820-14457870	NH-A	brain:	n/a
43	chr18:14458692-14458742	Hela-S3	cervix:	n/a
44	chr18:14458161-14458211	ProgFib	skin:	n/a
45	chr18:14459174-14459224	ECC-1	luminal epithelium:	n/a
46	chr18:14451035-14451085	K562	blood:	n/a
47	chr18:14451035-14451085	HUVEC	blood vessel:	n/a
48	chr18:14459174-14459224	BE2_C	brain:	n/a
49	chr18:14451035-14451085	PANC-1	pancreas:	n/a
50	chr18:14451035-14451085	HL-60	blood:	n/a

Variant related genes	Relation type
LONRF2P1	TF binding region
LONRF2P1	CpG island

Extended variants
information (count: 357 )
Associated
traits (count: 54 )

Variant overlapped rSNPs/rCNVs (count:357 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs537620302	chr18:14450495-14450496	Active TSS Enhancers Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs549609305	chr18:14450515-14450516	Active TSS Enhancers Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs561325653	chr18:14450527-14450528	Active TSS Enhancers Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs62080625	chr18:14450548-14450549	Active TSS Enhancers Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs530376159	chr18:14450601-14450602	Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs543772171	chr18:14450628-14450629	Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs562437169	chr18:14450650-14450651	Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs535592072	chr18:14450651-14450652	Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs531365400	chr18:14450780-14450781	Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs551489302	chr18:14450816-14450817	Active TSS Flanking Active TSS Bivalent/Poised TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs571408939	chr18:14450855-14450856	Active TSS Flanking Active TSS Bivalent/Poised TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs527493852	chr18:14450889-14450890	Active TSS Flanking Active TSS Bivalent/Poised TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs547524532	chr18:14450991-14450992	Active TSS Flanking Active TSS Bivalent/Poised TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs187032540	chr18:14451002-14451003	Weak transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs536514034	chr18:14451011-14451012	Weak transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs62080626	chr18:14451028-14451029	Weak transcription Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs193179019	chr18:14451036-14451037	Weak transcription Active TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
18	rs111869248	chr18:14451052-14451053	Weak transcription Active TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
19	rs111626226	chr18:14451058-14451059	Weak transcription Active TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
20	rs201139518	chr18:14451094-14451095	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs185294242	chr18:14451097-14451098	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs558622574	chr18:14451120-14451121	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs572455136	chr18:14451184-14451185	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs534815226	chr18:14451227-14451228	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs555107589	chr18:14451386-14451387	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs574953593	chr18:14451401-14451402	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs539083852	chr18:14451422-14451423	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs544109274	chr18:14451778-14451779	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs57819734	chr18:14451783-14451784	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs564008913	chr18:14451824-14451825	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs576099458	chr18:14451858-14451859	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs113061562	chr18:14451945-14451946	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs545072120	chr18:14451993-14451994	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs564730653	chr18:14452015-14452016	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs56853718	chr18:14452016-14452017	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs527340414	chr18:14452055-14452056	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs61240165	chr18:14452067-14452068	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs139024094	chr18:14452084-14452085	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs529882194	chr18:14452095-14452096	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs61212881	chr18:14452109-14452110	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs139841732	chr18:14452122-14452123	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs58794936	chr18:14452123-14452124	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs57857815	chr18:14452133-14452134	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs368325567	chr18:14452134-14452135	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs199617996	chr18:14452137-14452138	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs200628862	chr18:14452176-14452177	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs58707371	chr18:14452180-14452181	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs58107869	chr18:14452184-14452185	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs556445284	chr18:14452208-14452209	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs71365239	chr18:14452218-14452219	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:54)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
Intellectual disability	22102821	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Acute myeloid leukemia	16864856	CNVD
Seminomas	18059402	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Kartagener syndrome	16639409	CNVD
Basal cell lymphoma	21115979	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Cancer	21183584	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Basal cell lymphoma	17053054	CNVD
Colorectal cancer	19359472	CNVD
Human rectal carcinomas	16397240	CNVD
Melanoma	18172304	CNVD
Colorectal cancer	16272173	CNVD
Colorectal cancer	19150955	CNVD
Follicular lymphoma	20505157	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	18923191	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	21637783	CNVD
Medulloblastoma	21979893	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Trisomy 18 syndrome	17576883	CNVD
lymphocytic leukemia	21291569	CNVD
Barrett''s syndrome	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Ewing''s sarcoma	17952124	CNVD
Multiple myeloma	17550852	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Breast cancer	21364760	CNVD
Heart disease	21282601	CNVD
Glioblastoma multiforme	21922591	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Acute myeloid leukemia	17377590	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Lung cancer	18438408	CNVD
Breast cancer	16620391	CNVD
Myelofibrosis	22110671	CNVD
Retinoblastoma	21504564	CNVD
Glioma	17123091	CNVD
Neurodevelopmental disorder	22521361	CNVD
Breast cancer	21509527	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:172 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:14449600-14451000	Active TSS	HSMM	muscle
2	chr18:14450000-14450600	Enhancers	Primary T cells fromperipheralblood	blood
3	chr18:14450000-14451000	Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
4	chr18:14450000-14451000	Active TSS	Brain Germinal Matrix	brain
5	chr18:14450000-14451000	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
6	chr18:14450000-14451000	Active TSS	Colonic Mucosa	Colon
7	chr18:14450000-14451000	Active TSS	Colon Smooth Muscle	Colon
8	chr18:14450000-14451000	Active TSS	Fetal Brain Female	brain
9	chr18:14450000-14451200	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
10	chr18:14450200-14450800	Active TSS	Primary T regulatory cells fromperipheralblood	blood
11	chr18:14450200-14450800	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr18:14450200-14451000	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
13	chr18:14450200-14451000	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr18:14450200-14451000	Active TSS	Breast Myoepithelial Primary Cells	Breast
15	chr18:14450200-14451000	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
16	chr18:14450200-14451000	Active TSS	Muscle Satellite Cultured Cells	--
17	chr18:14450200-14451000	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
18	chr18:14450200-14451000	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
19	chr18:14450200-14451000	Bivalent/Poised TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
20	chr18:14450200-14451000	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
21	chr18:14450200-14451000	Active TSS	Adipose Nuclei	Adipose
22	chr18:14450200-14451000	Active TSS	Brain Angular Gyrus	brain
23	chr18:14450200-14451000	Active TSS	Brain Hippocampus Middle	brain
24	chr18:14450200-14451000	Active TSS	Duodenum Smooth Muscle	Duodenum
25	chr18:14450200-14451000	Active TSS	Esophagus	oesophagus
26	chr18:14450200-14451000	Active TSS	Left Ventricle	heart
27	chr18:14450200-14451000	Active TSS	Pancreas	Pancrea
28	chr18:14450200-14451000	Active TSS	Right Ventricle	heart
29	chr18:14450200-14451000	Active TSS	Skeletal Muscle Male	skeletal muscle
30	chr18:14450200-14451000	Active TSS	Skeletal Muscle Female	skeletal muscle
31	chr18:14450200-14451000	Active TSS	Stomach Smooth Muscle	stomach
32	chr18:14450200-14451200	Active TSS	HMEC	breast
33	chr18:14450200-14453400	Active TSS	Osteobl	bone
34	chr18:14450400-14450800	Active TSS	Primary mononuclear cells fromperipheralblood	Blood
35	chr18:14450400-14451000	Active TSS	iPS-18 Cell Line	embryonic stem cell
36	chr18:14450400-14451000	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
37	chr18:14450400-14451000	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
38	chr18:14450400-14451000	Active TSS	Primary hematopoietic stem cells	blood
39	chr18:14450400-14451000	Active TSS	Primary hematopoietic stem cells short term culture	blood
40	chr18:14450400-14451000	Active TSS	Primary T helper naive cells fromperipheralblood	blood
41	chr18:14450400-14451000	Active TSS	Primary T helper 17 cells PMA-I stimulated	--
42	chr18:14450400-14451000	Active TSS	Primary T helper cells fromperipheralblood	blood
43	chr18:14450400-14451000	Active TSS	Primary T killer naive cells fromperipheralblood	blood
44	chr18:14450400-14451000	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
45	chr18:14450400-14451000	Bivalent/Poised TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
46	chr18:14450400-14451000	Active TSS	Aorta	Aorta
47	chr18:14450400-14451000	Active TSS	Brain Anterior Caudate	brain
48	chr18:14450400-14451000	Active TSS	Brain Inferior Temporal Lobe	brain
49	chr18:14450400-14451000	Active TSS	Brain Substantia Nigra	brain
50	chr18:14450400-14451000	Active TSS	Duodenum Mucosa	Duodenum

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