Variant report

Variant	nsv1055343
Chromosome Location	chr18:12107012-12226356
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:588)
CpG islands
(count:0)
Chromatin interactive
region (count:12)
LncRNA
region (count:46)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:588 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr18:12200242-12200461	K562	blood:	n/a	n/a
2	BACH1	chr18:12121571-12121835	H1-hESC	embryonic stem cell:	n/a	n/a
3	BATF	chr18:12222072-12222359	GM12878	blood:	n/a	chr18:12222244-12222255
4	BATF	chr18:12200185-12200572	GM12878	blood:	n/a	chr18:12200380-12200391
5	BATF	chr18:12222054-12222440	GM12878	blood:	n/a	chr18:12222244-12222255
6	BATF	chr18:12199649-12200080	GM12878	blood:	n/a	n/a
7	BATF	chr18:12200183-12200545	GM12878	blood:	n/a	chr18:12200380-12200391
8	BCL11A	chr18:12180233-12180405	GM12878	blood:	n/a	n/a
9	BCL11A	chr18:12200159-12200559	GM12878	blood:	n/a	n/a
10	BCL11A	chr18:12222062-12222400	GM12878	blood:	n/a	n/a
11	BCL11A	chr18:12222065-12222401	GM12878	blood:	n/a	n/a
12	BCL11A	chr18:12200078-12200562	GM12878	blood:	n/a	chr18:12200149-12200156
13	BHLHE40	chr18:12180021-12180333	HepG2	liver:	n/a	n/a
14	BHLHE40	chr18:12121724-12122063	K562	blood:	n/a	n/a
15	BHLHE40	chr18:12200353-12200456	GM12878	blood:	n/a	n/a
16	CBX3	chr18:12208401-12208814	K562	blood:	n/a	n/a
17	CBX3	chr18:12200185-12200536	K562	blood:	n/a	n/a
18	CEBPB	chr18:12208436-12208770	K562	blood:	n/a	chr18:12208623-12208634
19	CEBPB	chr18:12119448-12119651	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr18:12114087-12114596	K562	blood:	n/a	chr18:12114424-12114435
21	CEBPB	chr18:12119385-12119733	K562	blood:	n/a	n/a
22	CEBPB	chr18:12110506-12111102	HepG2	liver:	n/a	n/a
23	CEBPB	chr18:12154647-12154741	HepG2	liver:	n/a	chr18:12154674-12154685
24	CEBPB	chr18:12114266-12114617	A549	lung:	n/a	chr18:12114424-12114435
25	CEBPB	chr18:12119384-12119757	K562	blood:	n/a	n/a
26	CEBPB	chr18:12150023-12150237	Hela-S3	cervix:	n/a	n/a
27	CEBPB	chr18:12208432-12208791	K562	blood:	n/a	chr18:12208623-12208634
28	CEBPB	chr18:12114135-12114617	HepG2	liver:	n/a	chr18:12114424-12114435
29	CEBPB	chr18:12114288-12114554	MCF-7	breast:	n/a	chr18:12114424-12114435
30	CEBPB	chr18:12150024-12150218	A549	lung:	n/a	n/a
31	CEBPB	chr18:12157358-12157635	HepG2	liver:	n/a	chr18:12157526-12157537
32	CEBPB	chr18:12114213-12114626	ECC-1	luminal epithelium:	n/a	chr18:12114424-12114435
33	CEBPB	chr18:12214692-12214750	Hela-S3	cervix:	n/a	n/a
34	CEBPB	chr18:12114189-12114605	IMR90	lung:	n/a	chr18:12114424-12114435
35	CEBPB	chr18:12114201-12114561	A549	lung:	n/a	chr18:12114424-12114435
36	CEBPB	chr18:12157404-12157659	A549	lung:	n/a	chr18:12157526-12157537
37	CEBPB	chr18:12114016-12114693	Hela-S3	cervix:	n/a	chr18:12114424-12114435
38	CEBPB	chr18:12114307-12114559	MCF-7	breast:	n/a	chr18:12114424-12114435
39	CEBPB	chr18:12154610-12154756	A549	lung:	n/a	chr18:12154674-12154685
40	CEBPB	chr18:12114249-12114616	H1-hESC	embryonic stem cell:	n/a	chr18:12114424-12114435
41	CEBPB	chr18:12150067-12150193	IMR90	lung:	n/a	n/a
42	CEBPB	chr18:12114060-12114567	K562	blood:	n/a	chr18:12114424-12114435
43	CEBPB	chr18:12208518-12208727	K562	blood:	n/a	chr18:12208623-12208634
44	CEBPD	chr18:12200168-12200539	K562	blood:	n/a	n/a
45	CTCF	chr18:12190031-12190063	GM13976	blood:	n/a	n/a
46	CTCF	chr18:12121247-12121449	HepG2	liver:	n/a	n/a
47	CTCF	chr18:12121300-12121450	HA-sp	spinal cord:	n/a	n/a
48	CTCF	chr18:12121361-12121428	GM19238	blood:	n/a	n/a
49	CTCF	chr18:12215588-12215610	K562	blood:	n/a	n/a
50	CTCF	chr18:12121307-12121469	MCF-7	breast:	n/a	n/a

No data

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr18:11979089..11980849-chr18:12109709..12111299,2	K562	blood:
2	chr18:12107653..12109609-chr18:12114882..12116934,2	K562	blood:
3	chr18:12119299..12121034-chr18:12123082..12124691,2	K562	blood:
4	chr18:12097992..12100907-chr18:12104911..12107291,2	MCF-7	breast:
5	chr18:12092475..12093363-chr18:12121230..12121778,4	MCF-7	breast:
6	chr18:12107653..12109609-chr18:12114882..12116934,2	K562	blood:
7	chr18:12119299..12121034-chr18:12123082..12124691,2	K562	blood:
8	chr18:12120897..12121609-chr22:17160804..17161481,3	MCF-7	breast:
9	chr18:10617533..10619309-chr18:12216627..12218573,2	K562	blood:
10	chr18:12094191..12096366-chr18:12113967..12116717,2	MCF-7	breast:
11	chr18:12120896..12121904-chr22:17160896..17161585,3	K562	blood:
12	chr18:12102586..12107654-chr18:12108102..12111487,4	K562	blood:

(count:46 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CIDEA-2	chr18:12197926-12198053	NONHSAT058348
2	lnc-CIDEA-2	chr18:12201953-12201978	ENSG00000267643.1
3	lnc-CIDEA-2	chr18:12201953-12202077	NONHSAT058349
4	lnc-CIDEA-2	chr18:12211851-12212071	NONHSAT058350
5	lnc-CIDEA-2	chr18:12218647-12218831	NONHSAT058352
6	lnc-CIDEA-2	chr18:12222799-12224701	XLOC_012630
7	lnc-CIDEA-2	chr18:12200330-12200570	NONHSAT058348
8	lnc-CIDEA-2	chr18:12209364-12209459	NONHSAT058349
9	lnc-CIDEA-2	chr18:12218698-12218831	XLOC_012630
10	lnc-CIDEA-2	chr18:12198516-12198669	NONHSAT058348
11	lnc-CIDEA-2	chr18:12218657-12218825	NONHSAT058354
12	lnc-ANKRD62-3	chr18:12179326-12179828	l_1532_chr18:12179325-12180756_testes
13	lnc-CIDEA-2	chr18:12222799-12224709	NONHSAT058349
14	lnc-ANKRD62-3	chr18:12180636-12180756	l_1532_chr18:12179325-12180756_testes
15	lnc-ANKRD62-3	chr18:12179860-12180358	l_1532_chr18:12179325-12180756_testes
16	lnc-CIDEA-2	chr18:12201981-12202077	NONHSAT058350
17	lnc-CIDEA-2	chr18:12197926-12198053	NONHSAT058346
18	lnc-CIDEA-2	chr18:12209364-12209429	NONHSAT058348
19	lnc-CIDEA-2	chr18:12209364-12209459	NONHSAT058350
20	lnc-CIDEA-2	chr18:12200778-12201173	NONHSAT058349
21	lnc-CIDEA-2	chr18:12191194-12191342	NONHSAT058348
22	lnc-CIDEA-2	chr18:12200778-12201173	ENSG00000267643.1
23	lnc-ANKRD62-4	chr18:12190636-12190977	NONHSAT058345
24	lnc-CIDEA-2	chr18:12201953-12202077	NONHSAT058348
25	lnc-CIDEA-2	chr18:12191194-12191342	NONHSAT058347
26	lnc-CIDEA-2	chr18:12197926-12198053	NONHSAT058347
27	lnc-CIDEA-6	chr18:12211377-12211806	NONHSAT058353
28	lnc-CIDEA-2	chr18:12214826-12214961	NONHSAT058354
29	lnc-CIDEA-2	chr18:12213406-12213596	NONHSAT058354
30	lnc-CIDEA-2	chr18:12201121-12201173	NONHSAT058348
31	lnc-CIDEA-2	chr18:12222799-12223538	NONHSAT058352
32	lnc-CIDEA-2	chr18:12191194-12191342	NONHSAT058346
33	lnc-CIDEA-2	chr18:12222799-12224800	XLOC_012630
34	lnc-CIDEA-2	chr18:12222775-12222997	NONHSAT058354
35	lnc-CIDEA-2	chr18:12211851-12212464	NONHSAT058351
36	lnc-CIDEA-2	chr18:12209335-12209459	NONHSAT058352
37	lnc-CIDEA-2	chr18:12218647-12218831	NONHSAT058349
38	lnc-CIDEA-2	chr18:12198516-12198669	NONHSAT058347
39	lnc-ANKRD62-4	chr18:12189748-12190358	NONHSAT058345
40	lnc-CIDEA-2	chr18:12218590-12218829	XLOC_012630
41	lnc-CIDEA-2	chr18:12198516-12199209	NONHSAT058346
42	lnc-CIDEA-2	chr18:12209364-12209459	NONHSAT058351
43	lnc-CIDEA-2	chr18:12208397-12208493	NONHSAT058351
44	lnc-CIDEA-2	chr18:12218590-12218842	XLOC_012630
45	lnc-CIDEA-2	chr18:12200333-12200601	NONHSAT058347
46	lnc-CIDEA-2	chr18:12222799-12224800	XLOC_012630

No data

Variant related genes	Relation type
ENSG00000267162	TF binding region
CCDC58P3	TF binding region
ENSG00000267733	TF binding region
ENSG00000267643	TF binding region
ENSG00000267116	TF binding region
ENSG00000200827	chromatin interactions
ENSG00000267478	chromatin interactions
ENSG00000181626	chromatin interactions

Extended variants
information (count: 3006 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:3006 , 50 per page) page: 1 2 3 4 5 6 7 ... 61

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs3923383	chr18:12107012-12107013	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs571730389	chr18:12107024-12107025	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs539188037	chr18:12107025-12107026	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs571763901	chr18:12107052-12107053	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs535954483	chr18:12107054-12107055	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs370490550	chr18:12107085-12107086	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs554137165	chr18:12107092-12107093	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs184278218	chr18:12107101-12107102	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs543331301	chr18:12107111-12107112	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs5823197	chr18:12107131-12107132	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs71172051	chr18:12107137-12107138	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs565220440	chr18:12107184-12107185	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs190399522	chr18:12107201-12107202	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs140879768	chr18:12107347-12107348	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs144813687	chr18:12107348-12107349	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs556039684	chr18:12107354-12107355	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs574585684	chr18:12107373-12107374	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs377391188	chr18:12107456-12107457	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs559358733	chr18:12108130-12108131	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs550948002	chr18:12108166-12108167	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs185700106	chr18:12108264-12108265	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs189014812	chr18:12108362-12108363	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs375049764	chr18:12108370-12108371	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs565147481	chr18:12108410-12108411	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs532833188	chr18:12108415-12108416	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs201885166	chr18:12108448-12108449	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs547734042	chr18:12108452-12108453	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs565913500	chr18:12108463-12108464	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs530265189	chr18:12108475-12108476	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs140344134	chr18:12108527-12108528	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs140430256	chr18:12108569-12108570	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs368329911	chr18:12108583-12108584	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs536754546	chr18:12108611-12108612	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs370870243	chr18:12108616-12108617	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs570399109	chr18:12108690-12108691	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs4619462	chr18:12108691-12108692	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs544885862	chr18:12108706-12108707	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs553334932	chr18:12108710-12108711	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs143449901	chr18:12108723-12108724	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs150868000	chr18:12108724-12108725	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs35056094	chr18:12108725-12108726	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs78681570	chr18:12108726-12108727	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs574798562	chr18:12108766-12108767	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs4417606	chr18:12108811-12108812	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
45	rs4417605	chr18:12108816-12108817	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
46	rs144123788	chr18:12108852-12108853	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs543596419	chr18:12108858-12108859	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs146488397	chr18:12108935-12108936	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs572818632	chr18:12109026-12109027	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs565280952	chr18:12109029-12109030	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:57)

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
Autism	20808228	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
small cell lung cancer	20016488	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
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Developmental delay	21147756	CNVD
Lung cancer	18438408	CNVD
Breast cancer	16620391	CNVD
Myelofibrosis	22110671	CNVD
Retinoblastoma	21504564	CNVD
Glioma	17123091	CNVD
Neurodevelopmental disorder	22521361	CNVD
Autism	20531469	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	19212409	CNVD

Chromatin state (count:94 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:12110200-12111600	Enhancers	Liver	Liver
2	chr18:12111600-12114400	Weak transcription	Liver	Liver
3	chr18:12113400-12114200	Enhancers	Pancreas	Pancrea
4	chr18:12114000-12114800	Enhancers	Breast Myoepithelial Primary Cells	Breast
5	chr18:12114000-12114800	Enhancers	Hela-S3	cervix
6	chr18:12114200-12130600	Weak transcription	Pancreas	Pancrea
7	chr18:12114400-12115800	Enhancers	Liver	Liver
8	chr18:12121400-12121600	Active TSS	HUES48 Cell Line	embryonic stem cell
9	chr18:12121400-12121600	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
10	chr18:12121400-12121600	Active TSS	HUES64 Cell Line	embryonic stem cell
11	chr18:12121400-12121800	Active TSS	ES-I3 Cell Line	embryonic stem cell
12	chr18:12121400-12121800	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr18:12121400-12121800	Active TSS	iPS-18 Cell Line	embryonic stem cell
14	chr18:12121400-12121800	Active TSS	iPS-20b Cell Line	embryonic stem cell
15	chr18:12121400-12121800	Enhancers	HepG2	liver
16	chr18:12121600-12121800	Enhancers	HUES6 Cell Line	embryonic stem cell
17	chr18:12121600-12121800	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
18	chr18:12121600-12122000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
19	chr18:12121600-12122000	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
20	chr18:12121600-12122000	Enhancers	iPS-15b Cell Line	embryonic stem cell
21	chr18:12121600-12122000	Enhancers	Primary monocytes fromperipheralblood	blood
22	chr18:12121800-12122000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr18:12121800-12122000	Enhancers	HUES64 Cell Line	embryonic stem cell
24	chr18:12121800-12122000	Bivalent Enhancer	HepG2	liver
25	chr18:12122000-12122400	Enhancers	HUES48 Cell Line	embryonic stem cell
26	chr18:12125800-12126000	Bivalent Enhancer	Sigmoid Colon	Sigmoid Colon
27	chr18:12133400-12133600	Enhancers	Fetal Heart	heart
28	chr18:12152200-12152600	Enhancers	iPS-18 Cell Line	embryonic stem cell
29	chr18:12152600-12153400	Enhancers	Psoas Muscle	Psoas
30	chr18:12152800-12153200	Enhancers	Skeletal Muscle Female	skeletal muscle
31	chr18:12154200-12183800	Weak transcription	Pancreas	Pancrea
32	chr18:12155400-12156000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
33	chr18:12157800-12158000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
34	chr18:12158000-12158200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
35	chr18:12159200-12160000	Enhancers	NHEK	skin
36	chr18:12159400-12159600	Enhancers	HepG2	liver
37	chr18:12160200-12160600	Enhancers	iPS-15b Cell Line	embryonic stem cell
38	chr18:12160200-12160800	Enhancers	HUES64 Cell Line	embryonic stem cell
39	chr18:12160200-12160800	Enhancers	iPS-18 Cell Line	embryonic stem cell
40	chr18:12160200-12160800	Enhancers	iPS-20b Cell Line	embryonic stem cell
41	chr18:12160200-12160800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
42	chr18:12161600-12163400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
43	chr18:12173000-12173200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
44	chr18:12173200-12175000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
45	chr18:12175000-12175200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
46	chr18:12179400-12179800	Enhancers	HepG2	liver
47	chr18:12195400-12196000	Enhancers	HUVEC	blood vessel
48	chr18:12195800-12196000	Enhancers	Skeletal Muscle Male	skeletal muscle
49	chr18:12195800-12198800	Weak transcription	Esophagus	oesophagus
50	chr18:12196600-12196800	Enhancers	Skeletal Muscle Male	skeletal muscle

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