Variant report

Variant	nsv1060448
Chromosome Location	chr18:30481131-30540347
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:720)
CpG islands
(count:61)
Chromatin interactive
region (count:18)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:720 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr18:30510663-30511023	HepG2	liver:	n/a	n/a
2	ARID3A	chr18:30501452-30501739	HepG2	liver:	n/a	n/a
3	ARID3A	chr18:30499794-30500195	HepG2	liver:	n/a	n/a
4	ATF1	chr18:30510749-30510935	K562	blood:	n/a	n/a
5	ATF2	chr18:30502920-30503305	GM12878	blood:	n/a	n/a
6	BACH1	chr18:30516693-30517043	H1-hESC	embryonic stem cell:	n/a	n/a
7	BHLHE40	chr18:30503054-30503254	GM12878	blood:	n/a	n/a
8	BHLHE40	chr18:30510763-30510997	GM12878	blood:	n/a	n/a
9	CCNT2	chr18:30486329-30486420	K562	blood:	n/a	n/a
10	CEBPB	chr18:30526711-30526869	HepG2	liver:	n/a	n/a
11	CEBPB	chr18:30500836-30501105	A549	lung:	n/a	chr18:30500944-30500955
12	CEBPB	chr18:30501501-30501761	A549	lung:	n/a	chr18:30501659-30501670
13	CEBPB	chr18:30490164-30490541	HepG2	liver:	n/a	chr18:30490237-30490245
14	CEBPB	chr18:30501423-30501831	ECC-1	luminal epithelium:	n/a	chr18:30501659-30501670
15	CEBPB	chr18:30526622-30526902	HepG2	liver:	n/a	n/a
16	CEBPB	chr18:30499791-30500141	HepG2	liver:	n/a	n/a
17	CEBPB	chr18:30518996-30519140	HepG2	liver:	n/a	n/a
18	CEBPB	chr18:30501416-30501805	HCT-116	colon:	n/a	chr18:30501659-30501670
19	CEBPB	chr18:30500870-30501015	HepG2	liver:	n/a	chr18:30500944-30500955
20	CEBPB	chr18:30526628-30526917	H1-hESC	embryonic stem cell:	n/a	n/a
21	CEBPB	chr18:30501473-30501857	ECC-1	luminal epithelium:	n/a	chr18:30501659-30501670
22	CEBPB	chr18:30490199-30490413	HepG2	liver:	n/a	chr18:30490237-30490245
23	CEBPB	chr18:30501471-30501840	HepG2	liver:	n/a	chr18:30501659-30501670
24	CEBPB	chr18:30500757-30501119	HepG2	liver:	n/a	chr18:30500944-30500955
25	CEBPB	chr18:30501453-30501831	IMR90	lung:	n/a	chr18:30501659-30501670
26	CEBPB	chr18:30499850-30500111	H1-hESC	embryonic stem cell:	n/a	n/a
27	CEBPB	chr18:30516859-30517065	H1-hESC	embryonic stem cell:	n/a	chr18:30516952-30516965
28	CEBPB	chr18:30510683-30510966	HepG2	liver:	n/a	n/a
29	CEBPB	chr18:30510693-30510988	Hela-S3	cervix:	n/a	n/a
30	CEBPB	chr18:30501420-30502206	Hela-S3	cervix:	n/a	chr18:30501659-30501670
31	CEBPB	chr18:30501563-30501737	HepG2	liver:	n/a	chr18:30501659-30501670
32	CTCF	chr18:30499819-30500096	A549	lung:	n/a	chr18:30499981-30500002 chr18:30499925-30499934
33	CTCF	chr18:30536620-30536770	WERI-Rb-1	eye:	n/a	n/a
34	CTCF	chr18:30499844-30500112	LNCaP	prostate:	n/a	chr18:30499981-30500002 chr18:30499925-30499934
35	CTCF	chr18:30536614-30536763	GM12878	blood:	n/a	n/a
36	CTCF	chr18:30510711-30511034	K562	blood:	n/a	n/a
37	CTCF	chr18:30499900-30500050	RPTEC	kidney:	n/a	chr18:30499981-30500002 chr18:30499925-30499934
38	CTCF	chr18:30536680-30536830	HVMF	connective:	n/a	n/a
39	CTCF	chr18:30499747-30500178	MCF-7	breast:	n/a	chr18:30499981-30500002 chr18:30499925-30499934
40	CTCF	chr18:30499880-30500030	Caco-2	colon:	n/a	chr18:30499981-30500002 chr18:30499925-30499934
41	CTCF	chr18:30499900-30500050	GM12868	blood:	n/a	chr18:30499981-30500002 chr18:30499925-30499934
42	CTCF	chr18:30536660-30536810	HPF	lung:	n/a	n/a
43	CTCF	chr18:30510780-30510930	SAEC	small airway:	n/a	n/a
44	CTCF	chr18:30510820-30510970	BE2_C	brain:	n/a	n/a
45	CTCF	chr18:30511001-30511032	GM13976	blood:	n/a	n/a
46	CTCF	chr18:30499820-30499970	HCT-116	colon:	n/a	chr18:30499925-30499934
47	CTCF	chr18:30510780-30510930	GM12873	blood:	n/a	n/a
48	CTCF	chr18:30510737-30510970	HepG2	liver:	n/a	n/a
49	CTCF	chr18:30510784-30510977	Kidney_OC	kidney:	n/a	n/a
50	CTCF	chr18:30510740-30510991	GM10248	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr18:30517666-30517716	HEK293	kidney:	embryo
2	chr18:30517666-30517716	SK-N-MC	brain:	n/a
3	chr18:30517666-30517716	NHDF-neo	bronchial:	n/a
4	chr18:30517666-30517716	HL-60	blood:	n/a
5	chr18:30517666-30517716	HMEC	breast:	n/a
6	chr18:30517666-30517716	HUVEC	blood vessel:	n/a
7	chr18:30517666-30517716	HCT-116	colon:	n/a
8	chr18:30517666-30517716	HCF	heart:	n/a
9	chr18:30517666-30517716	BJ	skin:	n/a
10	chr18:30517666-30517716	Hela-S3	cervix:	n/a
11	chr18:30517666-30517716	AG10803	skin:	n/a
12	chr18:30517666-30517716	GM06990	blood:	n/a
13	chr18:30517666-30517716	MCF10A-Er-Src	breast:	n/a
14	chr18:30517666-30517716	HRE	kidney:	n/a
15	chr18:30517666-30517716	PFSK-1	brain:	n/a
16	chr18:30517666-30517716	NB4	blood:	n/a
17	chr18:30517666-30517716	RPTEC	kidney:	n/a
18	chr18:30517666-30517716	SAEC	small airway:	n/a
19	chr18:30517666-30517716	AG09309	skin:	n/a
20	chr18:30517666-30517716	PANC-1	pancreas:	n/a
21	chr18:30517666-30517716	HCPEpiC	choroid plexus:	n/a
22	chr18:30517666-30517716	AG04449	skin:	fetal
23	chr18:30517666-30517716	AG09319	gingival:	n/a
24	chr18:30517666-30517716	U87	brain:	n/a
25	chr18:30517666-30517716	T-47D	breast:	n/a
26	chr18:30517666-30517716	HRCEpiC	kidney:	n/a
27	chr18:30517666-30517716	HCM	heart:	n/a
28	chr18:30517666-30517716	AG04450	lung:	fetal
29	chr18:30517666-30517716	CMK	blood:	n/a
30	chr18:30517666-30517716	IMR90	lung:	fetal
31	chr18:30517666-30517716	GM12878	blood:	n/a
32	chr18:30517666-30517716	HepG2	liver:	n/a
33	chr18:30517666-30517716	GM12892	blood:	n/a
34	chr18:30517666-30517716	AoSMC	blood vessel:	n/a
35	chr18:30517666-30517716	ECC-1	luminal epithelium:	n/a
36	chr18:30517666-30517716	HNPCEpiC	eye:	n/a
37	chr18:30517666-30517716	ProgFib	skin:	n/a
38	chr18:30517666-30517716	GM19239	blood:	n/a
39	chr18:30517666-30517716	SK-N-SH_RA	brain:	n/a
40	chr18:30517666-30517716	Caco-2	colon:	n/a
41	chr18:30517666-30517716	NH-A	brain:	n/a
42	chr18:30517666-30517716	Jurkat	blood:	n/a
43	chr18:30517666-30517716	MCF-7	breast:	n/a
44	chr18:30517666-30517716	SK-N-SH	brain:	n/a
45	chr18:30517666-30517716	ovcar-3	ovarian:	n/a
46	chr18:30517666-30517716	HRPEpiC	eye:	n/a
47	chr18:30517666-30517716	NHBE	bronchial:	n/a
48	chr18:30517666-30517716	SKMC	muscle:	n/a
49	chr18:30517666-30517716	HAEpiC	amniotic membrane:	n/a
50	chr18:30517666-30517716	NT2-D1	testis:	n/a

(count:18 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr18:30505715..30508318-chr18:30511122..30512749,2	MCF-7	breast:
2	chr18:30492890..30494424-chr18:30498589..30500639,2	MCF-7	breast:
3	chr18:30294270..30295293-chr18:30499582..30500548,5	MCF-7	breast:
4	chr18:30487680..30490056-chr18:30492113..30494145,2	K562	blood:
5	chr18:30482192..30483831-chr18:30485480..30487269,2	K562	blood:
6	chr18:30492146..30494495-chr18:30497517..30499760,2	K562	blood:
7	chr18:30517553..30519382-chr18:30521482..30523955,2	MCF-7	breast:
8	chr18:30505715..30508318-chr18:30511122..30512749,2	MCF-7	breast:
9	chr18:30479602..30480672-chr18:30499517..30500435,5	MCF-7	breast:
10	chr18:30479533..30480412-chr18:30499540..30500172,2	MCF-7	breast:
11	chr18:30294450..30295198-chr18:30499539..30500758,7	MCF-7	breast:
12	chr18:30293724..30294417-chr18:30499835..30500382,2	MCF-7	breast:
13	chr18:30492146..30494495-chr18:30497517..30499760,2	K562	blood:
14	chr18:30517553..30519382-chr18:30521482..30523955,2	MCF-7	breast:
15	chr18:30482192..30483831-chr18:30485480..30487269,2	K562	blood:
16	chr18:30487680..30490056-chr18:30492113..30494145,2	K562	blood:
17	chr18:30492890..30494424-chr18:30498589..30500639,2	MCF-7	breast:
18	chr18:30155970..30156491-chr18:30499440..30500054,2	MCF-7	breast:

(count:9 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC012123.1.1-2	chr18:30534039-30534050	ENSG00000263450.1
2	lnc-AC012123.1.1-1	chr18:30481478-30481714	NONHSAT058870
3	lnc-AC012123.1.1-1	chr18:30492797-30492928	ENSG00000263765.1
4	lnc-AC012123.1.1-2	chr18:30534470-30534611	ENSG00000263450.1
5	lnc-AC012123.1.1-1	chr18:30517950-30518280	ENSG00000263765.1
6	lnc-AC012123.1.1-2	chr18:30536598-30536774	ENSG00000263450.1
7	lnc-AC012123.1.1-2	chr18:30537736-30537962	ENSG00000263450.1
8	lnc-AC012123.1.1-1	chr18:30492858-30492929	NONHSAT058876
9	lnc-AC012123.1.1-1	chr18:30492797-30492821	NONHSAT058872

No data

Variant related genes	Relation type
ENSG00000263450	TF binding region
ENSG00000263450	CpG island

Extended variants
information (count: 1372 )
Associated
traits (count: 73 )

Variant overlapped rSNPs/rCNVs (count:1372 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs554978871	chr18:30481507-30481508	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
2	rs116461139	chr18:30481534-30481535	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
3	rs533878464	chr18:30481559-30481560	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
4	rs146130348	chr18:30481568-30481569	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
5	rs371795803	chr18:30481601-30481602	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
6	rs576638410	chr18:30481605-30481606	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
7	rs543958389	chr18:30481606-30481607	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
8	rs556010626	chr18:30481634-30481635	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
9	rs183824413	chr18:30481637-30481638	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
10	rs575139050	chr18:30481686-30481687	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
11	rs7228416	chr18:30481689-30481690	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs138885491	chr18:30481705-30481706	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
13	rs569334493	chr18:30482043-30482044	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs143834422	chr18:30482048-30482049	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs548388235	chr18:30482068-30482069	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs540329631	chr18:30482121-30482122	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs147237498	chr18:30482171-30482172	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs533893836	chr18:30482258-30482259	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs558433745	chr18:30482259-30482260	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs570387827	chr18:30482261-30482262	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs111977424	chr18:30482389-30482390	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs182452789	chr18:30482450-30482451	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs62090722	chr18:30482466-30482467	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs149372327	chr18:30482481-30482482	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs187360626	chr18:30482486-30482487	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs559767847	chr18:30482520-30482521	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs553578125	chr18:30482556-30482557	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs572071782	chr18:30482646-30482647	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs9949048	chr18:30482666-30482667	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs144802639	chr18:30482704-30482705	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs7235150	chr18:30482720-30482721	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs544553810	chr18:30482803-30482804	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs552136107	chr18:30482807-30482808	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs377531333	chr18:30482808-30482809	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs563141118	chr18:30482826-30482827	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs191750312	chr18:30482848-30482849	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs548670047	chr18:30482890-30482891	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs112767552	chr18:30482895-30482896	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs560339954	chr18:30482914-30482915	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs570252153	chr18:30482954-30482955	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs552120785	chr18:30483084-30483085	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs768140	chr18:30483094-30483095	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs181711439	chr18:30483109-30483110	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs374833414	chr18:30483111-30483112	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs115327933	chr18:30483117-30483118	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs571400858	chr18:30483125-30483126	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs76199648	chr18:30483143-30483144	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs148559843	chr18:30483256-30483257	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs569029934	chr18:30483270-30483271	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs572136866	chr18:30483355-30483356	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:73)

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
Pancreatic cancer	21811587	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Prostate cancer	22341455	CNVD

Chromatin state (count:230 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:30482000-30483200	Enhancers	Primary B cells from peripheral blood	blood
2	chr18:30482000-30483600	Enhancers	Primary B cells from cord blood	blood
3	chr18:30483200-30486600	Weak transcription	Primary B cells from peripheral blood	blood
4	chr18:30485400-30485800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr18:30485400-30485800	Enhancers	Ovary	ovary
6	chr18:30485400-30487600	Enhancers	Fetal Brain Male	brain
7	chr18:30485600-30489200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr18:30485800-30486000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
9	chr18:30485800-30486800	Weak transcription	Ovary	ovary
10	chr18:30485800-30489800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr18:30486000-30486800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
12	chr18:30486000-30487000	Enhancers	HMEC	breast
13	chr18:30486200-30487200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr18:30486400-30486600	Bivalent Enhancer	HepG2	liver
15	chr18:30486600-30487000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr18:30486600-30487000	Enhancers	Cortex derived primary cultured neurospheres	brain
17	chr18:30486600-30487000	Enhancers	Adipose Nuclei	Adipose
18	chr18:30486600-30488000	Enhancers	Primary B cells from peripheral blood	blood
19	chr18:30486800-30487000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
20	chr18:30486800-30487000	Enhancers	Ovary	ovary
21	chr18:30486800-30487400	Enhancers	Breast Myoepithelial Primary Cells	Breast
22	chr18:30487000-30487600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
23	chr18:30487000-30487800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
24	chr18:30487000-30490400	Weak transcription	HMEC	breast
25	chr18:30487200-30487600	Enhancers	Brain Hippocampus Middle	brain
26	chr18:30487200-30490400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
27	chr18:30487400-30487600	Bivalent Enhancer	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
28	chr18:30487400-30487600	Enhancers	Primary B cells from cord blood	blood
29	chr18:30487400-30487800	Enhancers	HepG2	liver
30	chr18:30487400-30488000	Enhancers	Brain Cingulate Gyrus	brain
31	chr18:30487400-30489800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
32	chr18:30487600-30487800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr18:30487600-30487800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
34	chr18:30487600-30488000	Enhancers	Brain Inferior Temporal Lobe	brain
35	chr18:30487600-30488400	Weak transcription	Primary B cells from cord blood	blood
36	chr18:30487800-30489800	Weak transcription	HepG2	liver
37	chr18:30487800-30490800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
38	chr18:30487800-30490800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
39	chr18:30488000-30488400	Weak transcription	Primary B cells from peripheral blood	blood
40	chr18:30488400-30488600	Bivalent Enhancer	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
41	chr18:30488400-30491200	Enhancers	Primary B cells from peripheral blood	blood
42	chr18:30488400-30492200	Enhancers	Primary B cells from cord blood	blood
43	chr18:30489200-30489600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
44	chr18:30489400-30491800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr18:30489600-30491000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
46	chr18:30489800-30490000	Enhancers	Breast Myoepithelial Primary Cells	Breast
47	chr18:30489800-30490600	Enhancers	NH-A	brain
48	chr18:30489800-30490800	Enhancers	HepG2	liver
49	chr18:30489800-30491000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
50	chr18:30490000-30490400	Weak transcription	Breast Myoepithelial Primary Cells	Breast

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