Variant report

Variant	esv3330159
Chromosome Location	chr18:29291412-29309318
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	ATF3	chr18:29291367-29291679	K562	blood:	n/a	n/a
2	BATF	chr18:29296336-29296604	GM12878	blood:	n/a	chr18:29296448-29296459
3	BHLHE40	chr18:29302347-29302630	GM12878	blood:	n/a	n/a
4	BHLHE40	chr18:29296347-29296627	GM12878	blood:	n/a	n/a
5	BHLHE40	chr18:29296070-29296072	GM12878	blood:	n/a	n/a
6	BHLHE40	chr18:29302383-29302699	K562	blood:	n/a	n/a
7	BRCA1	chr18:29302559-29302660	GM12878	blood:	n/a	n/a
8	CBX3	chr18:29299442-29299655	K562	blood:	n/a	n/a
9	CEBPB	chr18:29291409-29291740	A549	lung:	n/a	chr18:29291579-29291590 chr18:29291559-29291570 chr18:29291559-29291572 chr18:29291559-29291572
10	CEBPB	chr18:29291372-29291735	K562	blood:	n/a	chr18:29291579-29291590 chr18:29291559-29291570 chr18:29291559-29291572 chr18:29291559-29291572
11	CEBPB	chr18:29291466-29291663	K562	blood:	n/a	chr18:29291579-29291590 chr18:29291559-29291570 chr18:29291559-29291572 chr18:29291559-29291572
12	CEBPB	chr18:29291378-29291754	HepG2	liver:	n/a	chr18:29291579-29291590 chr18:29291559-29291570 chr18:29291559-29291572 chr18:29291559-29291572
13	CEBPB	chr18:29291412-29291660	H1-hESC	embryonic stem cell:	n/a	chr18:29291579-29291590 chr18:29291559-29291570 chr18:29291559-29291572 chr18:29291559-29291572
14	CEBPB	chr18:29291398-29291739	IMR90	lung:	n/a	chr18:29291579-29291590 chr18:29291559-29291570 chr18:29291559-29291572 chr18:29291559-29291572
15	CEBPB	chr18:29291376-29291752	Hela-S3	cervix:	n/a	chr18:29291579-29291590 chr18:29291559-29291570 chr18:29291559-29291572 chr18:29291559-29291572
16	CEBPB	chr18:29291377-29291764	K562	blood:	n/a	chr18:29291579-29291590 chr18:29291559-29291570 chr18:29291559-29291572 chr18:29291559-29291572
17	CHD2	chr18:29302407-29302694	H1-hESC	embryonic stem cell:	n/a	n/a
18	CHD2	chr18:29302415-29302581	GM12878	blood:	n/a	n/a
19	CTCF	chr18:29302416-29302663	Pancreas_OC	pancreas:	n/a	chr18:29302512-29302530 chr18:29302507-29302528 chr18:29302514-29302527
20	CTCF	chr18:29302460-29302610	AG09309	skin:	n/a	chr18:29302512-29302530 chr18:29302507-29302528 chr18:29302514-29302527
21	CTCF	chr18:29302460-29302610	AG04450	lung:	n/a	chr18:29302512-29302530 chr18:29302507-29302528 chr18:29302514-29302527
22	CTCF	chr18:29302409-29302682	MCF-7	breast:	n/a	chr18:29302512-29302530 chr18:29302507-29302528 chr18:29302514-29302527
23	CTCF	chr18:29302460-29302610	AG09319	gingival:	n/a	chr18:29302512-29302530 chr18:29302507-29302528 chr18:29302514-29302527
24	CTCF	chr18:29302460-29302610	GM12873	blood:	n/a	chr18:29302512-29302530 chr18:29302507-29302528 chr18:29302514-29302527
25	CTCF	chr18:29302400-29302550	HVMF	connective:	n/a	chr18:29302512-29302530 chr18:29302507-29302528 chr18:29302514-29302527
26	CTCF	chr18:29302460-29302610	GM12872	blood:	n/a	chr18:29302512-29302530 chr18:29302507-29302528 chr18:29302514-29302527
27	CTCF	chr18:29302460-29302610	AoAF	blood vessel:	n/a	chr18:29302512-29302530 chr18:29302507-29302528 chr18:29302514-29302527
28	CTCF	chr18:29302291-29302683	ECC-1	luminal epithelium:	n/a	chr18:29302512-29302530 chr18:29302507-29302528 chr18:29302514-29302527
29	CTCF	chr18:29302385-29302693	Gliobla	brain:	n/a	chr18:29302512-29302530 chr18:29302507-29302528 chr18:29302514-29302527
30	CTCF	chr18:29302440-29302590	HRE	kidney:	n/a	chr18:29302512-29302530 chr18:29302507-29302528 chr18:29302514-29302527
31	CTCF	chr18:29302440-29302590	HCPEpiC	choroid plexus:	n/a	chr18:29302512-29302530 chr18:29302507-29302528 chr18:29302514-29302527
32	CTCF	chr18:29304180-29304330	GM12874	blood:	n/a	n/a
33	CTCF	chr18:29302480-29302630	GM12871	blood:	n/a	chr18:29302512-29302530 chr18:29302507-29302528 chr18:29302514-29302527
34	CTCF	chr18:29302402-29302707	GM12892	blood:	n/a	chr18:29302512-29302530 chr18:29302507-29302528 chr18:29302514-29302527
35	CTCF	chr18:29302400-29302550	Caco-2	colon:	n/a	chr18:29302512-29302530 chr18:29302507-29302528 chr18:29302514-29302527
36	CTCF	chr18:29302480-29302630	K562	blood:	n/a	chr18:29302512-29302530 chr18:29302507-29302528 chr18:29302514-29302527
37	CTCF	chr18:29302408-29302688	Fibrobl	skin:	n/a	chr18:29302512-29302530 chr18:29302507-29302528 chr18:29302514-29302527
38	CTCF	chr18:29302365-29302663	HUVEC	blood vessel:	n/a	chr18:29302512-29302530 chr18:29302507-29302528 chr18:29302514-29302527
39	CTCF	chr18:29302440-29302590	GM12801	blood:	n/a	chr18:29302512-29302530 chr18:29302507-29302528 chr18:29302514-29302527
40	CTCF	chr18:29302420-29302570	GM12866	blood:	n/a	chr18:29302512-29302530 chr18:29302507-29302528 chr18:29302514-29302527
41	CTCF	chr18:29302440-29302590	GM12871	blood:	n/a	chr18:29302512-29302530 chr18:29302507-29302528 chr18:29302514-29302527
42	CTCF	chr18:29302420-29302570	GM12864	blood:	n/a	chr18:29302512-29302530 chr18:29302507-29302528 chr18:29302514-29302527
43	CTCF	chr18:29302431-29302662	MCF-7	breast:	n/a	chr18:29302512-29302530 chr18:29302507-29302528 chr18:29302514-29302527
44	CTCF	chr18:29302480-29302630	WERI-Rb-1	eye:	n/a	chr18:29302512-29302530 chr18:29302507-29302528 chr18:29302514-29302527
45	CTCF	chr18:29304400-29304550	GM12872	blood:	n/a	n/a
46	CTCF	chr18:29302382-29302707	Kidney_OC	kidney:	n/a	chr18:29302512-29302530 chr18:29302507-29302528 chr18:29302514-29302527
47	CTCF	chr18:29302440-29302590	GM12875	blood:	n/a	chr18:29302512-29302530 chr18:29302507-29302528 chr18:29302514-29302527
48	CTCF	chr18:29302460-29302610	RPTEC	kidney:	n/a	chr18:29302512-29302530 chr18:29302507-29302528 chr18:29302514-29302527
49	CTCF	chr18:29302460-29302610	AG04449	skin:	n/a	chr18:29302512-29302530 chr18:29302507-29302528 chr18:29302514-29302527
50	CTCF	chr18:29302440-29302590	HL-60	blood:	n/a	chr18:29302512-29302530 chr18:29302507-29302528 chr18:29302514-29302527

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr18:29304818-29304868	HCM	heart:	n/a
2	chr18:29304253-29304303	BJ	skin:	n/a
3	chr18:29304111-29304161	SK-N-SH	brain:	n/a
4	chr18:29304818-29304868	HCM	heart:	n/a
5	chr18:29304253-29304303	BJ	skin:	n/a
6	chr18:29304111-29304161	SK-N-SH	brain:	n/a
7	chr18:29307959-29308009	PFSK-1	brain:	n/a
8	chr18:29304253-29304303	Caco-2	colon:	n/a
9	chr18:29304253-29304303	ECC-1	luminal epithelium:	n/a
10	chr18:29304111-29304161	HRE	kidney:	n/a
11	chr18:29304253-29304303	Hela-S3	cervix:	n/a
12	chr18:29302528-29302578	HRE	kidney:	n/a
13	chr18:29302528-29302578	RPTEC	kidney:	n/a
14	chr18:29304253-29304303	Hepatocyte	liver:	n/a
15	chr18:29304111-29304161	K562	blood:	n/a
16	chr18:29304253-29304303	Jurkat	blood:	n/a
17	chr18:29304253-29304303	H1-hESC	embryonic stem cell:	embryo
18	chr18:29304111-29304161	IMR90	lung:	fetal
19	chr18:29304253-29304303	ovcar-3	ovarian:	n/a
20	chr18:29304818-29304868	K562	blood:	n/a
21	chr18:29300658-29300708	AG04449	skin:	fetal
22	chr18:29302528-29302578	GM12878	blood:	n/a
23	chr18:29307959-29308009	GM12891	blood:	n/a
24	chr18:29304818-29304868	HRE	kidney:	n/a
25	chr18:29304482-29304532	SAEC	small airway:	n/a
26	chr18:29307959-29308009	HEK293	kidney:	embryo
27	chr18:29304111-29304161	HUVEC	blood vessel:	n/a
28	chr18:29304818-29304868	GM06990	blood:	n/a
29	chr18:29304818-29304868	RPTEC	kidney:	n/a
30	chr18:29304111-29304161	PFSK-1	brain:	n/a
31	chr18:29304253-29304303	GM12878	blood:	n/a
32	chr18:29304482-29304532	Jurkat	blood:	n/a
33	chr18:29307959-29308009	PANC-1	pancreas:	n/a
34	chr18:29304111-29304161	HNPCEpiC	eye:	n/a
35	chr18:29304253-29304303	SK-N-SH	brain:	n/a
36	chr18:29307959-29308009	RPTEC	kidney:	n/a
37	chr18:29302528-29302578	HMEC	breast:	n/a
38	chr18:29302528-29302578	MCF-7	breast:	n/a
39	chr18:29304818-29304868	HEEpiC	esophagus:	n/a
40	chr18:29304482-29304532	A549	lung:	n/a
41	chr18:29304111-29304161	GM06990	blood:	n/a
42	chr18:29302528-29302578	T-47D	breast:	n/a
43	chr18:29307959-29308009	MCF-7	breast:	n/a
44	chr18:29304818-29304868	ovcar-3	ovarian:	n/a
45	chr18:29307959-29308009	A549	lung:	n/a
46	chr18:29304482-29304532	K562	blood:	n/a
47	chr18:29304482-29304532	BJ	skin:	n/a
48	chr18:29307959-29308009	SK-N-MC	brain:	n/a
49	chr18:29300658-29300708	AoSMC	blood vessel:	n/a
50	chr18:29304111-29304161	NB4	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr18:29290630..29291464-chr18:29399315..29400108,2	MCF-7	breast:
2	chr18:29275310..29278274-chr18:29291077..29293888,2	MCF-7	breast:
3	chr18:29078002..29079523-chr18:29301802..29303631,2	K562	blood:
4	chr18:29264959..29265684-chr18:29302461..29303010,2	MCF-7	breast:
5	chr18:29135071..29136376-chr18:29302039..29303290,3	MCF-7	breast:
6	chr18:29264481..29265444-chr18:29302123..29302943,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TTR-2	chr18:29298856-29299171	NONHSAT058831
2	lnc-TTR-3	chr18:29304161-29306919	NONHSAT058832
3	lnc-TTR-3	chr18:29304782-29305727	NONHSAT058833
4	lnc-TTR-3	chr18:29304191-29304638	NONHSAT058833

Variant related genes	Relation type
LRRC37A7P	TF binding region
RN7SKP44	TF binding region
ENSG00000263772	TF binding region
LRRC37A7P	CpG island
RN7SKP44	CpG island
ENSG00000263772	CpG island
ENSG00000118276	chromatin interactions
ENSG00000259985	chromatin interactions
ENSG00000046604	chromatin interactions

Extended variants
information (count: 627 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:627 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs535695081	chr18:29291454-29291455	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs564982183	chr18:29291520-29291521	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs553698235	chr18:29291542-29291543	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs565327465	chr18:29291551-29291552	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs539080606	chr18:29291587-29291588	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs557352728	chr18:29291651-29291652	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs576053722	chr18:29291750-29291751	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs536754563	chr18:29291794-29291795	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs137958643	chr18:29291821-29291822	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs187288811	chr18:29291849-29291850	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs542530110	chr18:29291869-29291870	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs7241853	chr18:29291940-29291941	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs560798865	chr18:29291942-29291943	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs11661766	chr18:29291975-29291976	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs572447506	chr18:29292012-29292013	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs546194446	chr18:29292027-29292028	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs564341424	chr18:29292102-29292103	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs12326689	chr18:29292118-29292119	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs113728524	chr18:29292214-29292215	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs191419389	chr18:29292225-29292226	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs368495996	chr18:29292231-29292232	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs374888377	chr18:29292248-29292249	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs576995191	chr18:29292249-29292250	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs202123146	chr18:29292250-29292251	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs78011598	chr18:29292268-29292269	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs71175786	chr18:29292271-29292272	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs561918843	chr18:29292344-29292345	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs183612074	chr18:29292394-29292395	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs547274776	chr18:29292419-29292420	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs149516007	chr18:29292436-29292437	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs539362740	chr18:29292442-29292443	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs188705170	chr18:29292448-29292449	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs12605982	chr18:29292455-29292456	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs537146267	chr18:29292539-29292540	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs555209341	chr18:29292542-29292543	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs148243124	chr18:29292568-29292569	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs558065535	chr18:29292569-29292570	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs12326719	chr18:29292627-29292628	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs536080547	chr18:29292639-29292640	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs554426232	chr18:29292680-29292681	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs117204661	chr18:29292737-29292738	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs192844873	chr18:29292784-29292785	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs185741785	chr18:29292793-29292794	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs141883017	chr18:29292810-29292811	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs543891336	chr18:29292831-29292832	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs529933282	chr18:29292833-29292834	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs562075404	chr18:29292862-29292863	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs187696348	chr18:29292870-29292871	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs1667296	chr18:29292925-29292926	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
50	rs373057866	chr18:29292980-29292981	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:68)

Disease	PMID	Source
Esophageal squamous carcinoma	18350619	CNVD
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
Glioblastoma multiforme	21922591	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
Lung cancer	18438408	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
Hepatocellular carcinoma	16750200	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
Breast cancer	17133270	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Colorectal cancer	16774939	CNVD
Colorectal cancer	21297112	CNVD
Myelofibrosis	22110671	CNVD
Colorectal cancer	21645411	CNVD
Glioblastoma multiforme	17002787	CNVD
Cancer	21183584	CNVD
Breast cancer	17603634	CNVD
Thyroid cancer	19087340	CNVD
Urothelial carcinoma	21177765	CNVD
Oral cancer	21386901	CNVD
Colorectal cancer	16912164	CNVD
Renal cell carcinoma	19150565	CNVD
Multiple myeloma	16616336	CNVD
Colorectal cancer	19150955	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21364760	CNVD

Chromatin state (count:314 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:29290400-29292000	Enhancers	Primary neutrophils fromperipheralblood	blood
2	chr18:29290400-29292200	Enhancers	K562	blood
3	chr18:29290600-29298400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr18:29290800-29292000	Enhancers	Primary monocytes fromperipheralblood	blood
5	chr18:29291000-29292600	Weak transcription	Aorta	Aorta
6	chr18:29291000-29300200	Weak transcription	Psoas Muscle	Psoas
7	chr18:29291200-29300400	Weak transcription	Skeletal Muscle Female	skeletal muscle
8	chr18:29291400-29291800	Enhancers	Monocytes-CD14+_RO01746	blood
9	chr18:29292000-29292200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr18:29292200-29298200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr18:29293000-29293200	Enhancers	Aorta	Aorta
12	chr18:29293000-29293600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
13	chr18:29293200-29293400	Enhancers	Esophagus	oesophagus
14	chr18:29293200-29293600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr18:29293200-29293600	Enhancers	HMEC	breast
16	chr18:29293200-29293800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
17	chr18:29293200-29293800	Enhancers	NHEK	skin
18	chr18:29293400-29293800	Active TSS	Pancreatic Islets	Pancreatic Islet
19	chr18:29293600-29293800	Enhancers	Breast Myoepithelial Primary Cells	Breast
20	chr18:29293800-29294600	Weak transcription	Pancreatic Islets	Pancreatic Islet
21	chr18:29293800-29297000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
22	chr18:29294600-29294800	Enhancers	Pancreatic Islets	Pancreatic Islet
23	chr18:29295800-29296200	Enhancers	Fetal Intestine Small	intestine
24	chr18:29295800-29297200	Enhancers	Fetal Intestine Large	intestine
25	chr18:29296000-29296400	Enhancers	GM12878-XiMat	blood
26	chr18:29296400-29296600	Enhancers	Adipose Nuclei	Adipose
27	chr18:29296600-29298200	Weak transcription	Adipose Nuclei	Adipose
28	chr18:29298200-29298600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
29	chr18:29298200-29298600	Enhancers	Adipose Nuclei	Adipose
30	chr18:29298200-29299000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
31	chr18:29298400-29299400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
32	chr18:29298800-29299400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
33	chr18:29299000-29300600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
34	chr18:29299200-29299600	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin03	Skin
35	chr18:29299400-29300200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
36	chr18:29299600-29303400	Weak transcription	Stomach Smooth Muscle	stomach
37	chr18:29299600-29303600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
38	chr18:29299800-29303400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
39	chr18:29299800-29303400	Weak transcription	Brain Anterior Caudate	brain
40	chr18:29300000-29302600	Weak transcription	Liver	Liver
41	chr18:29300200-29300600	Enhancers	Psoas Muscle	Psoas
42	chr18:29300200-29300800	Enhancers	Left Ventricle	heart
43	chr18:29300200-29301000	Enhancers	Placenta Amnion	Placenta Amnion
44	chr18:29300200-29301200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
45	chr18:29300200-29302000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
46	chr18:29300400-29301000	Enhancers	Skeletal Muscle Female	skeletal muscle
47	chr18:29300600-29300800	Enhancers	Esophagus	oesophagus
48	chr18:29300600-29303600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
49	chr18:29300600-29303800	Weak transcription	Psoas Muscle	Psoas
50	chr18:29300800-29301200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin

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