Variant report

Variant	esv15009
Chromosome Location	chr18:44222960-44263857
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	ARID3A	chr18:44238219-44238551	HepG2	liver:	n/a	n/a
2	ARID3A	chr18:44238235-44238505	K562	blood:	n/a	n/a
3	ATF2	chr18:44238063-44238497	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr18:44238058-44238485	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF3	chr18:44241019-44241345	H1-hESC	embryonic stem cell:	n/a	n/a
6	BHLHE40	chr18:44238235-44238525	GM12878	blood:	n/a	n/a
7	BHLHE40	chr18:44238127-44238398	K562	blood:	n/a	n/a
8	CCNT2	chr18:44236769-44236886	K562	blood:	n/a	n/a
9	CEBPB	chr18:44255105-44255297	H1-hESC	embryonic stem cell:	n/a	chr18:44255238-44255249
10	CEBPB	chr18:44255110-44255279	K562	blood:	n/a	chr18:44255238-44255249
11	CEBPB	chr18:44256579-44256590	H1-hESC	embryonic stem cell:	n/a	n/a
12	CEBPB	chr18:44255086-44255385	A549	lung:	n/a	chr18:44255238-44255249
13	CEBPB	chr18:44255078-44255409	Hela-S3	cervix:	n/a	chr18:44255238-44255249
14	CEBPB	chr18:44255065-44255429	HepG2	liver:	n/a	chr18:44255238-44255249
15	CEBPB	chr18:44255084-44255402	IMR90	lung:	n/a	chr18:44255238-44255249
16	CHD1	chr18:44238036-44238454	H1-hESC	embryonic stem cell:	n/a	n/a
17	CHD1	chr18:44238155-44238632	IMR90	lung:	n/a	n/a
18	CHD2	chr18:44240999-44241303	H1-hESC	embryonic stem cell:	n/a	n/a
19	CHD2	chr18:44238077-44238490	H1-hESC	embryonic stem cell:	n/a	n/a
20	CTCF	chr18:44243240-44243390	GM12870	blood:	n/a	n/a
21	CTCF	chr18:44257720-44257870	GM06990	blood:	n/a	chr18:44257811-44257832 chr18:44257809-44257827
22	CTCF	chr18:44238340-44238490	HEEpiC	esophagus:	n/a	chr18:44238425-44238438 chr18:44238423-44238441 chr18:44238424-44238440 chr18:44238425-44238438
23	CTCF	chr18:44226604-44226668	GM19238	blood:	n/a	n/a
24	CTCF	chr18:44257760-44257910	HCPEpiC	choroid plexus:	n/a	chr18:44257811-44257832 chr18:44257809-44257827
25	CTCF	chr18:44257760-44257910	AG09309	skin:	n/a	chr18:44257811-44257832 chr18:44257809-44257827
26	CTCF	chr18:44232521-44232584	GM12878	blood:	n/a	n/a
27	CTCF	chr18:44257702-44257891	HepG2	liver:	n/a	chr18:44257811-44257832 chr18:44257809-44257827
28	CTCF	chr18:44257700-44257850	GM12873	blood:	n/a	chr18:44257811-44257832 chr18:44257809-44257827
29	CTCF	chr18:44257800-44257950	HPAF	blood vessel:	n/a	chr18:44257811-44257832 chr18:44257809-44257827
30	CTCF	chr18:44238360-44238510	GM12867	blood:	n/a	chr18:44238425-44238438 chr18:44238423-44238441 chr18:44238424-44238440 chr18:44238425-44238438
31	CTCF	chr18:44257737-44257874	GM10266	blood:	n/a	chr18:44257811-44257832 chr18:44257809-44257827
32	CTCF	chr18:44237920-44238070	GM12873	blood:	n/a	n/a
33	CTCF	chr18:44257740-44257890	BJ	skin:	n/a	chr18:44257811-44257832 chr18:44257809-44257827
34	CTCF	chr18:44239440-44239465	GM20000	blood:	n/a	n/a
35	CTCF	chr18:44238380-44238530	NHLF	lung:	n/a	chr18:44238425-44238438 chr18:44238423-44238441 chr18:44238424-44238440 chr18:44238425-44238438
36	CTCF	chr18:44238340-44238490	GM12867	blood:	n/a	chr18:44238425-44238438 chr18:44238423-44238441 chr18:44238424-44238440 chr18:44238425-44238438
37	CTCF	chr18:44243180-44243330	GM12868	blood:	n/a	n/a
38	CTCF	chr18:44232504-44232579	Hela-S3	cervix:	n/a	n/a
39	CTCF	chr18:44257747-44257883	H1-hESC	embryonic stem cell:	n/a	chr18:44257811-44257832 chr18:44257809-44257827
40	CTCF	chr18:44257719-44257894	GM12878	blood:	n/a	chr18:44257811-44257832 chr18:44257809-44257827
41	CTCF	chr18:44238280-44238430	HUVEC	blood vessel:	n/a	n/a
42	CTCF	chr18:44238380-44238530	GM12864	blood:	n/a	chr18:44238425-44238438 chr18:44238423-44238441 chr18:44238424-44238440 chr18:44238425-44238438
43	CTCF	chr18:44238101-44238645	GM12878	blood:	n/a	chr18:44238425-44238438 chr18:44238279-44238288 chr18:44238276-44238294 chr18:44238423-44238441 chr18:44238278-44238299 chr18:44238279-44238292 chr18:44238424-44238440 chr18:44238425-44238438 chr18:44238277-44238293
44	CTCF	chr18:44238380-44238530	AoAF	blood vessel:	n/a	chr18:44238425-44238438 chr18:44238423-44238441 chr18:44238424-44238440 chr18:44238425-44238438
45	CTCF	chr18:44257692-44257905	ProgFib	skin:	n/a	chr18:44257811-44257832 chr18:44257809-44257827
46	CTCF	chr18:44238320-44238470	GM12801	blood:	n/a	chr18:44238425-44238438 chr18:44238423-44238441 chr18:44238424-44238440 chr18:44238425-44238438
47	CTCF	chr18:44243260-44243410	GM12873	blood:	n/a	n/a
48	CTCF	chr18:44257640-44257790	NHEK	skin:	n/a	n/a
49	CTCF	chr18:44257720-44257870	HepG2	liver:	n/a	chr18:44257811-44257832 chr18:44257809-44257827
50	CTCF	chr18:44238340-44238490	GM12873	blood:	n/a	chr18:44238425-44238438 chr18:44238423-44238441 chr18:44238424-44238440 chr18:44238425-44238438

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr18:44256337-44256387	SK-N-SH	brain:	n/a
2	chr18:44260450-44260500	HCM	heart:	n/a
3	chr18:44236918-44236968	K562	blood:	n/a
4	chr18:44235125-44235175	HRCEpiC	kidney:	n/a
5	chr18:44237151-44237201	Jurkat	blood:	n/a
6	chr18:44259973-44260023	HAEpiC	amniotic membrane:	n/a
7	chr18:44259787-44259837	HUVEC	blood vessel:	n/a
8	chr18:44237151-44237201	HNPCEpiC	eye:	n/a
9	chr18:44237093-44237143	Caco-2	colon:	n/a
10	chr18:44237019-44237069	HEK293	kidney:	embryo
11	chr18:44237619-44237669	A549	lung:	n/a
12	chr18:44237019-44237069	SK-N-SH_RA	brain:	n/a
13	chr18:44259787-44259837	Hepatocyte	liver:	n/a
14	chr18:44237023-44237073	HIPEpiC	eye:	n/a
15	chr18:44237023-44237073	MCF10A-Er-Src	breast:	n/a
16	chr18:44236847-44236897	BE2_C	brain:	n/a
17	chr18:44237151-44237201	ECC-1	luminal epithelium:	n/a
18	chr18:44241006-44241056	HepG2	liver:	n/a
19	chr18:44260450-44260500	AG09319	gingival:	n/a
20	chr18:44237023-44237073	SK-N-SH_RA	brain:	n/a
21	chr18:44237023-44237073	HRPEpiC	eye:	n/a
22	chr18:44260450-44260500	PrEC	prostate:	n/a
23	chr18:44235125-44235175	HNPCEpiC	eye:	n/a
24	chr18:44237801-44237851	HIPEpiC	eye:	n/a
25	chr18:44241006-44241056	AoSMC	blood vessel:	n/a
26	chr18:44256337-44256387	HIPEpiC	eye:	n/a
27	chr18:44235125-44235175	NB4	blood:	n/a
28	chr18:44237619-44237669	H1-hESC	embryonic stem cell:	embryo
29	chr18:44236847-44236897	Jurkat	blood:	n/a
30	chr18:44260091-44260141	Hela-S3	cervix:	n/a
31	chr18:44237019-44237069	AG10803	skin:	n/a
32	chr18:44237019-44237069	Hela-S3	cervix:	n/a
33	chr18:44235125-44235175	A549	lung:	n/a
34	chr18:44260357-44260407	PrEC	prostate:	n/a
35	chr18:44259973-44260023	ECC-1	luminal epithelium:	n/a
36	chr18:44235125-44235175	AG10803	skin:	n/a
37	chr18:44237087-44237137	ovcar-3	ovarian:	n/a
38	chr18:44259787-44259837	HAEpiC	amniotic membrane:	n/a
39	chr18:44256337-44256387	HRE	kidney:	n/a
40	chr18:44237023-44237073	SKMC	muscle:	n/a
41	chr18:44259973-44260023	HIPEpiC	eye:	n/a
42	chr18:44234815-44234865	HCM	heart:	n/a
43	chr18:44234815-44234865	Hela-S3	cervix:	n/a
44	chr18:44234815-44234865	AoSMC	blood vessel:	n/a
45	chr18:44234815-44234865	PFSK-1	brain:	n/a
46	chr18:44259973-44260023	K562	blood:	n/a
47	chr18:44260048-44260098	ProgFib	skin:	n/a
48	chr18:44259973-44260023	MCF-7	breast:	n/a
49	chr18:44237093-44237143	HRE	kidney:	n/a
50	chr18:44237093-44237143	A549	lung:	n/a

No.	Distal block	Cell Line	Cell type
1	chr18:44233210..44235377-chr18:44237809..44240707,2	K562	blood:
2	chr18:44025629..44026494-chr18:44238265..44238771,2	MCF-7	breast:
3	chr18:44255000..44257936-chr18:44258609..44260874,2	K562	blood:
4	chr18:44255000..44257936-chr18:44258609..44260874,2	K562	blood:
5	chr18:43861250..43861755-chr18:44237903..44238816,2	K562	blood:
6	chr18:44140391..44141193-chr18:44238367..44238874,2	K562	blood:
7	chr18:44202977..44203585-chr18:44237863..44238863,2	MCF-7	breast:
8	chr18:44241101..44243679-chr18:44244362..44246685,2	MCF-7	breast:
9	chr18:44255901..44257936-chr18:44259374..44261657,2	K562	blood:
10	chr18:44135472..44136540-chr18:44237677..44238574,5	MCF-7	breast:
11	chr18:44241101..44243679-chr18:44244362..44246685,2	MCF-7	breast:
12	chr18:44233210..44235377-chr18:44237809..44240707,2	K562	blood:
13	chr18:43861183..43862185-chr18:44237910..44238891,3	MCF-7	breast:
14	chr18:44135421..44136286-chr18:44237959..44238787,2	K562	blood:
15	chr18:44255901..44257936-chr18:44259374..44261657,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ST8SIA5-1	chr18:44247785-44248874	NONHSAT059135
2	lnc-ST8SIA5-1	chr18:44255878-44256829	NONHSAT059135
3	lnc-ST8SIA5-1	chr18:44247785-44250252	NONHSAT059134

Variant related genes	Relation type
LOXHD1	TF binding region
LOXHD1	CpG island

Extended variants
information (count: 1141 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:1141 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs190101752	chr18:44222967-44222968	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs373369091	chr18:44222984-44222985	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs11874730	chr18:44222993-44222994	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs115594603	chr18:44222996-44222997	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs182363534	chr18:44223040-44223041	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs74384095	chr18:44223078-44223079	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs570142463	chr18:44223110-44223111	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs534308973	chr18:44223178-44223179	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs554491098	chr18:44223185-44223186	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs566242379	chr18:44223199-44223200	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs186599943	chr18:44223209-44223210	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs145769057	chr18:44223256-44223257	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs576678267	chr18:44223270-44223271	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs664633	chr18:44223280-44223281	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs543958839	chr18:44223312-44223313	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs533189533	chr18:44223318-44223319	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs550443401	chr18:44223321-44223322	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs193103850	chr18:44223358-44223359	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs328171	chr18:44223365-44223366	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs577347923	chr18:44223393-44223394	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs570302525	chr18:44223399-44223400	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs202149837	chr18:44229023-44229024	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs539041173	chr18:44229060-44229061	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs546596031	chr18:44229088-44229089	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs374277176	chr18:44229113-44229114	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs200306249	chr18:44229132-44229133	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs547806908	chr18:44229140-44229141	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs34763877	chr18:44229159-44229160	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs566538334	chr18:44229165-44229166	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs199536893	chr18:44229166-44229167	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs116413527	chr18:44229186-44229187	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs374871163	chr18:44229187-44229188	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs200763838	chr18:44229197-44229198	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs377414885	chr18:44229199-44229200	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs371836452	chr18:44229279-44229280	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs368570855	chr18:44229292-44229293	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs557748383	chr18:44229310-44229311	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs78039210	chr18:44229358-44229359	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs559787959	chr18:44229392-44229393	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs540231316	chr18:44229438-44229439	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs560547495	chr18:44229450-44229451	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs573751305	chr18:44229456-44229457	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs144702623	chr18:44229469-44229470	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs562682736	chr18:44229484-44229485	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs328180	chr18:44229485-44229486	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs545611786	chr18:44229503-44229504	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs181768225	chr18:44229524-44229525	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs565410875	chr18:44229576-44229577	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs8093186	chr18:44229581-44229582	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs565457738	chr18:44229640-44229641	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:90)

Disease	PMID	Source
Follicular lymphoma	20505157	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	18923191	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Chronic lymphocytic leukemia	21546498	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
Ewing''s sarcoma	17952124	CNVD
Multiple myeloma	17550852	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Melanoma	18172304	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
18q deletion syndrome	19533772	CNVD
Acute myeloid leukemia	16864856	CNVD
Colorectal cancer	21102417	CNVD
Colorectal cancer	20709793	CNVD
Pancreatic cancer	21811562	CNVD
Basal cell lymphoma	21115979	CNVD
Mucosa-associated lymphoid tissue lymphomas	21459788	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Oligodendroglial tumors	17285580	CNVD
colon cancer	17210682	CNVD
Breast cancer	21785460	CNVD
Prostate cancer	16573809	CNVD
Autism	16446308	CNVD
Colorectal cancer	19359472	CNVD
Colorectal cancer	16272173	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	18056178	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Cancer	16751803	CNVD
Metanephric adenoma	20802469	CNVD
small cell lung cancer	20016488	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Colorectal cancer	21297112	CNVD
Breast cancer	17603634	CNVD
Thyroid cancer	19087340	CNVD
Urothelial carcinoma	21177765	CNVD
Oral cancer	21386901	CNVD
Colorectal cancer	19150955	CNVD
Acute myeloid leukemia	21251322	CNVD
Colorectal cancer	16912164	CNVD
Lung cancer	18438408	CNVD
Seminomas	18059402	CNVD
Breast cancer	16272173	CNVD
Breast cancer	17133270	CNVD
prenatal diagnosis	22389664	CNVD
Medulloblastoma	16783165	CNVD
Neuroblastoma	21508638	CNVD
Myelofibrosis	22110671	CNVD
Multiple myeloma	16461302	CNVD
Chronic lymphocytic leukemia	21049055	CNVD
Breast cancer	16397240	CNVD
Non-small cell lung cancer	21829676	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Pilomyxoid astrocytoma	17436254	CNVD
Mental retardation	21062444	CNVD
Cancer	21183584	CNVD
Burkitt''s lymphoma	18698080	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Cancer	17160897	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Gastric cancer	16891809	CNVD
Idiopathic thrombocytopenic purpura	19566914	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16774939	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Lung cancer	21569311	CNVD
Prostate cancer	22341455	CNVD
small cell lung cancer	17426248	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:215 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:44221800-44223200	Enhancers	Fetal Muscle Leg	muscle
2	chr18:44222000-44223400	Enhancers	Fetal Muscle Trunk	muscle
3	chr18:44229000-44230000	Enhancers	Fetal Heart	heart
4	chr18:44229200-44230200	Enhancers	Left Ventricle	heart
5	chr18:44234600-44235000	Enhancers	Dnd41	blood
6	chr18:44235000-44238000	Weak transcription	Dnd41	blood
7	chr18:44235400-44235600	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr18:44235400-44235600	Enhancers	Primary hematopoietic stem cells short term culture	blood
9	chr18:44235600-44237200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
10	chr18:44236200-44237200	Active TSS	Brain Anterior Caudate	brain
11	chr18:44236400-44237000	Enhancers	HUES6 Cell Line	embryonic stem cell
12	chr18:44236600-44237800	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
13	chr18:44236800-44237000	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
14	chr18:44236800-44237800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
15	chr18:44236800-44238000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr18:44237000-44237200	Enhancers	iPS-15b Cell Line	embryonic stem cell
17	chr18:44237000-44237200	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
18	chr18:44237000-44238200	Active TSS	ES-WA7 Cell Line	embryonic stem cell
19	chr18:44237000-44238200	Enhancers	H1 Cell Line	embryonic stem cell
20	chr18:44237000-44238200	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
21	chr18:44237200-44237600	Enhancers	Primary hematopoietic stem cells short term culture	blood
22	chr18:44237200-44237800	Active TSS	iPS-15b Cell Line	embryonic stem cell
23	chr18:44237400-44237600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
24	chr18:44237400-44238000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
25	chr18:44237600-44238200	Enhancers	HUES64 Cell Line	embryonic stem cell
26	chr18:44237600-44238400	Enhancers	Fetal Muscle Trunk	muscle
27	chr18:44237800-44238200	Flanking Bivalent TSS/Enh	ES-I3 Cell Line	embryonic stem cell
28	chr18:44237800-44238200	Enhancers	HUES48 Cell Line	embryonic stem cell
29	chr18:44237800-44238200	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
30	chr18:44237800-44238200	Enhancers	iPS-18 Cell Line	embryonic stem cell
31	chr18:44237800-44238400	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
32	chr18:44238000-44238400	Enhancers	Primary T killer memory cells from peripheral blood	blood
33	chr18:44238000-44238400	Enhancers	Dnd41	blood
34	chr18:44238000-44238400	Enhancers	HepG2	liver
35	chr18:44238000-44240200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
36	chr18:44238200-44238400	Enhancers	Fetal Brain Male	brain
37	chr18:44238200-44238400	Bivalent Enhancer	Placenta	Placenta
38	chr18:44238200-44238400	Bivalent Enhancer	Fetal Stomach	stomach
39	chr18:44238200-44241000	Weak transcription	H1 Cell Line	embryonic stem cell
40	chr18:44238400-44240800	Weak transcription	Fetal Brain Male	brain
41	chr18:44240200-44240400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
42	chr18:44240200-44241400	Enhancers	Brain Germinal Matrix	brain
43	chr18:44240400-44240800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
44	chr18:44240600-44241400	Enhancers	Brain Angular Gyrus	brain
45	chr18:44240600-44241600	Enhancers	Brain Cingulate Gyrus	brain
46	chr18:44240600-44241600	Enhancers	Skeletal Muscle Female	skeletal muscle
47	chr18:44240800-44241200	Enhancers	Fetal Brain Male	brain
48	chr18:44240800-44241400	Enhancers	HSMM	muscle
49	chr18:44240800-44241600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
50	chr18:44240800-44241600	Enhancers	Brain Hippocampus Middle	brain

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