Variant report

Variant	nsv576449
Chromosome Location	chr18:9623052-9700382
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1634)
CpG islands
(count:0)
Chromatin interactive
region (count:151)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1634 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr18:9673566-9673708	K562	blood:	n/a	n/a
2	ARID3A	chr18:9681184-9681707	K562	blood:	n/a	n/a
3	ARID3A	chr18:9683342-9683695	HepG2	liver:	n/a	n/a
4	ARID3A	chr18:9683339-9683651	K562	blood:	n/a	n/a
5	ARID3A	chr18:9683964-9684466	K562	blood:	n/a	n/a
6	ARID3A	chr18:9674285-9674540	HepG2	liver:	n/a	n/a
7	ARID3A	chr18:9673267-9673782	HepG2	liver:	n/a	n/a
8	ARID3A	chr18:9685491-9685629	K562	blood:	n/a	n/a
9	ARID3A	chr18:9643479-9643914	HepG2	liver:	n/a	n/a
10	ATF1	chr18:9681188-9681607	K562	blood:	n/a	n/a
11	ATF2	chr18:9643422-9644012	H1-hESC	embryonic stem cell:	n/a	n/a
12	ATF2	chr18:9643358-9643991	H1-hESC	embryonic stem cell:	n/a	n/a
13	ATF2	chr18:9673142-9673880	GM12878	blood:	n/a	n/a
14	ATF2	chr18:9673170-9673886	GM12878	blood:	n/a	n/a
15	ATF3	chr18:9643511-9644002	HCT-116	colon:	n/a	n/a
16	ATF3	chr18:9673169-9673758	A549	lung:	n/a	n/a
17	ATF3	chr18:9681204-9681437	K562	blood:	n/a	n/a
18	BACH1	chr18:9673371-9673379	K562	blood:	n/a	n/a
19	BACH1	chr18:9681284-9681578	K562	blood:	n/a	n/a
20	BACH1	chr18:9688634-9688637	K562	blood:	n/a	n/a
21	BACH1	chr18:9694260-9694493	H1-hESC	embryonic stem cell:	n/a	n/a
22	BATF	chr18:9673165-9673761	GM12878	blood:	n/a	n/a
23	BATF	chr18:9696048-9696276	GM12878	blood:	n/a	n/a
24	BATF	chr18:9648787-9649181	GM12878	blood:	n/a	n/a
25	BATF	chr18:9673220-9673688	GM12878	blood:	n/a	n/a
26	BCL11A	chr18:9643614-9643824	H1-hESC	embryonic stem cell:	n/a	n/a
27	BCL11A	chr18:9673165-9673621	GM12878	blood:	n/a	n/a
28	BCL11A	chr18:9643538-9643886	H1-hESC	embryonic stem cell:	n/a	n/a
29	BCL11A	chr18:9673154-9673764	GM12878	blood:	n/a	n/a
30	BCL3	chr18:9673245-9673745	GM12878	blood:	n/a	n/a
31	BCLAF1	chr18:9673150-9673892	GM12878	blood:	n/a	n/a
32	BCLAF1	chr18:9673141-9673913	GM12878	blood:	n/a	n/a
33	BHLHE40	chr18:9648954-9649112	GM12878	blood:	n/a	n/a
34	BHLHE40	chr18:9685039-9685546	K562	blood:	n/a	n/a
35	BHLHE40	chr18:9673447-9673794	K562	blood:	n/a	n/a
36	BHLHE40	chr18:9648531-9648623	A549	lung:	n/a	n/a
37	BHLHE40	chr18:9673186-9673806	GM12878	blood:	n/a	n/a
38	BHLHE40	chr18:9683905-9684357	K562	blood:	n/a	n/a
39	BHLHE40	chr18:9688001-9688476	K562	blood:	n/a	chr18:9688153-9688162 chr18:9688153-9688162
40	BHLHE40	chr18:9681197-9681571	K562	blood:	n/a	n/a
41	BHLHE40	chr18:9687998-9688355	HepG2	liver:	n/a	chr18:9688153-9688162 chr18:9688153-9688162
42	BRCA1	chr18:9631792-9632198	Hela-S3	cervix:	n/a	n/a
43	BRCA1	chr18:9673182-9673964	Hela-S3	cervix:	n/a	n/a
44	BRCA1	chr18:9658385-9658650	Hela-S3	cervix:	n/a	n/a
45	CBX3	chr18:9673082-9673965	HCT-116	colon:	n/a	n/a
46	CBX3	chr18:9635636-9636222	K562	blood:	n/a	n/a
47	CBX3	chr18:9683415-9684428	K562	blood:	n/a	n/a
48	CBX3	chr18:9634840-9635405	K562	blood:	n/a	n/a
49	CBX3	chr18:9684860-9685599	K562	blood:	n/a	chr18:9684940-9684951
50	CEBPB	chr18:9684117-9684377	K562	blood:	n/a	n/a

No data

(count:151 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type
1	chr18:9657868..9660660-chr18:9663836..9666305,2	MCF-7	breast:
2	chr18:9674934..9676991-chr18:9682664..9686574,3	K562	blood:
3	chr18:9690985..9692984-chr18:9695409..9697746,2	MCF-7	breast:
4	chr18:9612628..9617891-chr18:9619605..9623342,5	MCF-7	breast:
5	chr18:9613984..9616177-chr18:9626000..9628106,2	K562	blood:
6	chr18:9692274..9695093-chr18:9912664..9914388,2	K562	blood:
7	chr18:9613237..9615569-chr18:9690826..9693390,2	MCF-7	breast:
8	chr18:9613565..9616099-chr18:9658301..9661880,4	K562	blood:
9	chr18:9680525..9686114-chr18:9707690..9711025,4	MCF-7	breast:
10	chr18:9663594..9667478-chr18:9668646..9672937,5	K562	blood:
11	chr18:9696780..9700512-chr18:9912998..9916299,4	K562	blood:
12	chr18:9610247..9612763-chr18:9683592..9685519,2	K562	blood:
13	chr18:9683599..9684594-chr18:9771436..9772119,2	MCF-7	breast:
14	chr18:9613070..9618286-chr18:9641748..9647088,7	MCF-7	breast:
15	chr18:9645776..9648945-chr18:9653255..9655530,3	K562	blood:
16	chr18:9613656..9616076-chr18:9629019..9630972,2	K562	blood:
17	chr18:9682384..9686964-chr18:9702727..9705542,5	K562	blood:
18	chr18:9629058..9631077-chr18:9650339..9653253,2	K562	blood:
19	chr18:9690985..9692984-chr18:9695409..9697746,2	MCF-7	breast:
20	chr18:9684035..9684686-chr18:9792389..9793128,3	MCF-7	breast:
21	chr18:9575357..9576099-chr18:9683070..9683881,4	MCF-7	breast:
22	chr18:9612709..9618416-chr18:9656954..9662874,9	MCF-7	breast:
23	chr18:9643919..9647276-chr18:9653045..9655313,3	K562	blood:
24	chr18:9687189..9690124-chr18:9701130..9704989,3	K562	blood:
25	chr18:9691473..9693462-chr18:9695947..9698084,2	K562	blood:
26	chr18:9613080..9618986-chr18:9672487..9675941,11	MCF-7	breast:
27	chr18:9695131..9695661-chr18:9722812..9723326,2	MCF-7	breast:
28	chr18:9613087..9615055-chr18:9684050..9685628,2	K562	blood:
29	chr18:9653164..9654681-chr18:9657331..9659688,2	MCF-7	breast:
30	chr18:9686215..9688324-chr18:9694336..9696864,2	K562	blood:
31	chr18:9612188..9615434-chr18:9650562..9653752,4	MCF-7	breast:
32	chr18:9671775..9674338-chr18:9683094..9685173,2	K562	blood:
33	chr18:9629058..9631077-chr18:9650339..9653253,2	K562	blood:
34	chr18:9612064..9613483-chr18:9661140..9662203,5	MCF-7	breast:
35	chr18:9684225..9686490-chr18:9771447..9773237,2	K562	blood:
36	chr18:9686886..9688402-chr18:9740468..9742300,2	K562	blood:
37	chr18:9640413..9642046-chr18:9643613..9646688,3	K562	blood:
38	chr18:9627468..9629148-chr18:9631077..9633967,2	MCF-7	breast:
39	chr18:9647445..9649188-chr18:9652519..9654755,2	K562	blood:
40	chr18:9695119..9697370-chr18:9698845..9701098,2	K562	blood:
41	chr18:9638107..9640165-chr18:9648278..9650768,2	K562	blood:
42	chr18:9671374..9674373-chr18:9705168..9708061,3	MCF-7	breast:
43	chr18:9640413..9642046-chr18:9643613..9646688,3	K562	blood:
44	chr18:9677449..9679645-chr18:9682253..9684229,2	K562	blood:
45	chr18:9627920..9630651-chr18:9632769..9635738,3	K562	blood:
46	chr18:9613504..9616306-chr18:9671786..9673528,2	K562	blood:
47	chr18:9670935..9675283-chr18:9677129..9681931,4	K562	blood:
48	chr18:9658398..9660624-chr18:9662930..9664815,2	K562	blood:
49	chr18:9613601..9616129-chr18:9653955..9656678,4	MCF-7	breast:
50	chr18:9694556..9698075-chr18:9707259..9709265,3	K562	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RAB31-2	chr18:9637984-9638340	l_1523_chr18:9636235-9638327_testes
2	lnc-RAB31-1	chr18:9647984-9648542	XLOC_012623
3	lnc-RAB31-1	chr18:9646153-9646560	XLOC_012623
4	lnc-RAB31-2	chr18:9636236-9636560	l_1523_chr18:9636235-9638327_testes

No data

Variant related genes	Relation type
RNU6-903P	TF binding region
KRT18P8	TF binding region
ENSG00000101558	chromatin interactions
ENSG00000272799	chromatin interactions
ENSG00000168461	chromatin interactions
ENSG00000264644	chromatin interactions
ENSG00000263627	chromatin interactions
ENSG00000154845	chromatin interactions
ENSG00000212572	chromatin interactions

Extended variants
information (count: 3242 )
Associated
traits (count: 56 )

Variant overlapped rSNPs/rCNVs (count:3242 , 50 per page) page: 1 2 3 4 5 6 7 ... 65

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs589559	chr18:9623052-9623053	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs181864614	chr18:9623058-9623059	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs79160083	chr18:9623067-9623068	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs546485961	chr18:9623072-9623073	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs559751501	chr18:9623086-9623087	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs186940687	chr18:9623121-9623122	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs144103800	chr18:9623225-9623226	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs60571867	chr18:9623250-9623251	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs575968943	chr18:9623256-9623257	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs11872850	chr18:9623257-9623258	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs191184120	chr18:9623316-9623317	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs532393669	chr18:9623332-9623333	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs541230983	chr18:9623336-9623337	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs559554363	chr18:9623367-9623368	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs34097738	chr18:9623368-9623369	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs544984492	chr18:9623374-9623375	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs530239358	chr18:9623393-9623394	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs148723011	chr18:9623418-9623419	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs569986197	chr18:9623454-9623455	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs9948354	chr18:9623553-9623554	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs563194000	chr18:9623560-9623561	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs57884105	chr18:9623579-9623580	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs111983461	chr18:9623597-9623598	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs570815541	chr18:9623603-9623604	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs534947691	chr18:9623640-9623641	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs28817058	chr18:9623698-9623699	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs8090919	chr18:9623708-9623709	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
28	rs372707120	chr18:9623773-9623774	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs535989863	chr18:9623799-9623800	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs546875325	chr18:9623814-9623815	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs531953495	chr18:9623823-9623824	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs554632076	chr18:9623853-9623854	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs28861672	chr18:9623872-9623873	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs12958744	chr18:9623927-9623928	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs7231696	chr18:9623938-9623939	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs145607113	chr18:9623977-9623978	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs372983065	chr18:9624034-9624035	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs185369418	chr18:9624056-9624057	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs2903503	chr18:9624068-9624069	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs537962513	chr18:9624100-9624101	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs189729448	chr18:9624107-9624108	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs112668097	chr18:9624108-9624109	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs530865878	chr18:9624113-9624114	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs552553619	chr18:9624124-9624125	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs577572047	chr18:9624129-9624130	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs564102558	chr18:9624170-9624171	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs182187107	chr18:9624173-9624174	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs546866031	chr18:9624227-9624228	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs369320426	chr18:9624266-9624267	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs188024505	chr18:9624319-9624320	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:56)

Disease	PMID	Source
Melanoma	18172304	CNVD
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
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
Breast cancer	21785460	CNVD
Autism	20808228	CNVD
lymphocytic leukemia	21291569	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Barrett''s syndrome	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
Multiple myeloma	17550852	CNVD
Developmental delay	21147756	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21858162	CNVD
small cell lung cancer	20016488	CNVD
abnormal development	18461090	CNVD
Heart disease	21282601	CNVD
Glioblastoma multiforme	21922591	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Acute myeloid leukemia	17377590	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Lung cancer	18438408	CNVD
Melanoma	20877625	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:1137 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:9615800-9625200	Weak transcription	Placenta	Placenta
2	chr18:9615800-9625400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr18:9615800-9627400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
4	chr18:9617400-9625400	Weak transcription	HMEC	breast
5	chr18:9617600-9630600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr18:9619800-9627400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
7	chr18:9620000-9625400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
8	chr18:9620000-9625600	Weak transcription	Hela-S3	cervix
9	chr18:9620000-9627200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
10	chr18:9620000-9627400	Weak transcription	HUES6 Cell Line	embryonic stem cell
11	chr18:9620000-9627600	Weak transcription	NHDF-Ad	bronchial
12	chr18:9620200-9623800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
13	chr18:9620200-9625200	Weak transcription	NHEK	skin
14	chr18:9620200-9625400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
15	chr18:9620200-9625600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
16	chr18:9620200-9627000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
17	chr18:9620200-9627400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
18	chr18:9620200-9627400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
19	chr18:9620200-9627400	Weak transcription	NHLF	lung
20	chr18:9620200-9627400	Weak transcription	Osteobl	bone
21	chr18:9620800-9627600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
22	chr18:9625200-9626400	Enhancers	Placenta	Placenta
23	chr18:9625200-9628200	Enhancers	NHEK	skin
24	chr18:9625400-9625800	Enhancers	HMEC	breast
25	chr18:9625400-9626200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
26	chr18:9625400-9626200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
27	chr18:9625400-9626400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
28	chr18:9625600-9625800	Enhancers	Placenta Amnion	Placenta Amnion
29	chr18:9625600-9626000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
30	chr18:9625600-9628200	Enhancers	Hela-S3	cervix
31	chr18:9625800-9627200	Weak transcription	HMEC	breast
32	chr18:9625800-9627400	Weak transcription	Placenta Amnion	Placenta Amnion
33	chr18:9626000-9627600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
34	chr18:9626200-9627400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
35	chr18:9626200-9628200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
36	chr18:9626400-9626800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
37	chr18:9626400-9628000	Weak transcription	Placenta	Placenta
38	chr18:9626800-9628000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
39	chr18:9627000-9628000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
40	chr18:9627000-9628200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
41	chr18:9627200-9627800	Enhancers	ES-I3 Cell Line	embryonic stem cell
42	chr18:9627200-9628000	Enhancers	iPS-20b Cell Line	embryonic stem cell
43	chr18:9627200-9628000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
44	chr18:9627200-9628200	Enhancers	HMEC	breast
45	chr18:9627400-9627600	Enhancers	A549	lung
46	chr18:9627400-9627800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
47	chr18:9627400-9627800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
48	chr18:9627400-9628000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr18:9627400-9628000	Enhancers	HUES48 Cell Line	embryonic stem cell
50	chr18:9627400-9628000	Enhancers	iPS-18 Cell Line	embryonic stem cell

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