Variant report

Variant	nsv833601
Chromosome Location	chr18:24908240-25080975
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	ATF1	chr18:24982163-24982172	K562	blood:	n/a	n/a
2	ATF1	chr18:25050948-25051253	K562	blood:	n/a	n/a
3	ATF1	chr18:24954083-24954161	K562	blood:	n/a	n/a
4	ATF1	chr18:25022305-25022445	K562	blood:	n/a	n/a
5	BACH1	chr18:25003448-25003451	K562	blood:	n/a	n/a
6	BACH1	chr18:25071917-25071941	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr18:25077720-25077810	K562	blood:	n/a	n/a
8	BATF	chr18:24958371-24958665	GM12878	blood:	n/a	n/a
9	BHLHE40	chr18:25042021-25042178	K562	blood:	n/a	n/a
10	BHLHE40	chr18:25028034-25028066	GM12878	blood:	n/a	n/a
11	BHLHE40	chr18:24958353-24958708	GM12878	blood:	n/a	n/a
12	CCNT2	chr18:24910086-24910358	K562	blood:	n/a	n/a
13	CEBPB	chr18:24991794-24991831	H1-hESC	embryonic stem cell:	n/a	chr18:24991796-24991807
14	CEBPB	chr18:24969942-24970015	HepG2	liver:	n/a	n/a
15	CEBPB	chr18:24944047-24944233	HepG2	liver:	n/a	n/a
16	CEBPB	chr18:24947874-24948074	HepG2	liver:	n/a	chr18:24947918-24947929
17	CEBPB	chr18:24944016-24944247	H1-hESC	embryonic stem cell:	n/a	n/a
18	CEBPB	chr18:24991657-24991903	HepG2	liver:	n/a	chr18:24991796-24991807
19	CEBPB	chr18:24977211-24977474	HepG2	liver:	n/a	chr18:24977345-24977356
20	CEBPB	chr18:24963754-24963955	K562	blood:	n/a	n/a
21	CEBPB	chr18:24963736-24963936	A549	lung:	n/a	n/a
22	CHD2	chr18:25071836-25071868	H1-hESC	embryonic stem cell:	n/a	n/a
23	CHD2	chr18:25050236-25050311	H1-hESC	embryonic stem cell:	n/a	n/a
24	CHD2	chr18:24958420-24958738	GM12878	blood:	n/a	chr18:24958567-24958577
25	CREB1	chr18:24958290-24958703	GM12878	blood:	n/a	n/a
26	CTCF	chr18:24943911-24944241	K562	blood:	n/a	chr18:24944066-24944082 chr18:24944065-24944083 chr18:24944067-24944088 chr18:24944069-24944076
27	CTCF	chr18:24980067-24980213	GM12891	blood:	n/a	n/a
28	CTCF	chr18:24980000-24980150	HEEpiC	esophagus:	n/a	n/a
29	CTCF	chr18:24944040-24944190	SK-N-SH_RA	brain:	n/a	chr18:24944066-24944082 chr18:24944065-24944083 chr18:24944067-24944088 chr18:24944069-24944076
30	CTCF	chr18:25008420-25008570	RPTEC	kidney:	n/a	n/a
31	CTCF	chr18:24980080-24980230	HEK293	kidney:	n/a	n/a
32	CTCF	chr18:24980062-24980222	HepG2	liver:	n/a	n/a
33	CTCF	chr18:24944040-24944190	NHEK	skin:	n/a	chr18:24944066-24944082 chr18:24944065-24944083 chr18:24944067-24944088 chr18:24944069-24944076
34	CTCF	chr18:25013755-25013944	GM12878	blood:	n/a	n/a
35	CTCF	chr18:24979960-24980110	HRPEpiC	eye:	n/a	n/a
36	CTCF	chr18:24980040-24980190	HAc	cerebellar:	n/a	n/a
37	CTCF	chr18:24943940-24944090	NHEK	skin:	n/a	chr18:24944066-24944082 chr18:24944065-24944083 chr18:24944067-24944088 chr18:24944069-24944076
38	CTCF	chr18:24980060-24980210	GM12878	blood:	n/a	n/a
39	CTCF	chr18:24980080-24980230	HBMEC	blood vessel:	n/a	n/a
40	CTCF	chr18:24980040-24980190	GM12865	blood:	n/a	n/a
41	CTCF	chr18:25008160-25008310	HCPEpiC	choroid plexus:	n/a	n/a
42	CTCF	chr18:24944040-24944190	AG10803	skin:	n/a	chr18:24944066-24944082 chr18:24944065-24944083 chr18:24944067-24944088 chr18:24944069-24944076
43	CTCF	chr18:24980050-24980214	Kidney_OC	kidney:	n/a	n/a
44	CTCF	chr18:24944040-24944190	HEK293	kidney:	n/a	chr18:24944066-24944082 chr18:24944065-24944083 chr18:24944067-24944088 chr18:24944069-24944076
45	CTCF	chr18:24944000-24944150	AG04449	skin:	n/a	chr18:24944066-24944082 chr18:24944065-24944083 chr18:24944067-24944088 chr18:24944069-24944076
46	CTCF	chr18:24943982-24944145	Pancreas_OC	pancreas:	n/a	chr18:24944066-24944082 chr18:24944065-24944083 chr18:24944067-24944088 chr18:24944069-24944076
47	CTCF	chr18:24944000-24944150	GM06990	blood:	n/a	chr18:24944066-24944082 chr18:24944065-24944083 chr18:24944067-24944088 chr18:24944069-24944076
48	CTCF	chr18:24966140-24966290	HEK293	kidney:	n/a	n/a
49	CTCF	chr18:24980120-24980270	SAEC	small airway:	n/a	n/a
50	CTCF	chr18:24943940-24944210	GM12864	blood:	n/a	chr18:24944066-24944082 chr18:24944065-24944083 chr18:24944067-24944088 chr18:24944069-24944076

No.	Distal block	Cell Line	Cell type
1	chr18:25069473..25070359-chr5:103536312..103537041,2	MCF-7	breast:
2	chr18:24943676..24944460-chr18:25007824..25008627,3	MCF-7	breast:
3	chr18:25045399..25047199-chr18:25047889..25050274,2	K562	blood:
4	chr18:24943675..24944656-chr18:25178856..25179868,5	MCF-7	breast:
5	chr18:24973172..24976079-chr18:24978347..24981182,2	K562	blood:
6	chr18:24977247..24980260-chr18:24984681..24986773,3	K562	blood:
7	chr18:24954918..24958816-chr18:24960045..24962711,3	K562	blood:
8	chr18:24917748..24920423-chr18:24922458..24924248,2	K562	blood:
9	chr18:24973172..24976079-chr18:24978347..24981182,2	K562	blood:
10	chr18:25060579..25062895-chr18:25064603..25067042,2	K562	blood:
11	chr18:24954918..24958816-chr18:24960045..24962711,3	K562	blood:
12	chr18:25045399..25047199-chr18:25047889..25050274,2	K562	blood:
13	chr18:24905897..24907565-chr18:24911708..24913896,2	K562	blood:
14	chr18:25060579..25062895-chr18:25064603..25067042,2	K562	blood:
15	chr18:25023772..25025471-chr18:25027335..25029107,2	K562	blood:
16	chr18:25023772..25025471-chr18:25027335..25029107,2	K562	blood:
17	chr18:24943983..24944563-chr18:25178918..25179433,2	MCF-7	breast:
18	chr18:24943676..24944460-chr18:25007824..25008627,3	MCF-7	breast:
19	chr18:24962546..24965411-chr18:24970882..24973457,2	K562	blood:
20	chr18:24968333..24970148-chr18:24971946..24974816,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CDH2-2	chr18:24918571-24918666	ENSG00000264151.1
2	lnc-CDH2-2	chr18:24922467-24922654	ENSG00000264151.1
3	lnc-TAF4B-6	chr18:24924185-24924306	ENSG00000264790.1
4	lnc-TAF4B-7	chr18:24981464-24981868	ENSG00000263611.1
5	lnc-CDH2-2	chr18:24918571-24918743	ENSG00000264151.1
6	lnc-CDH2-2	chr18:24916657-24917151	ENSG00000264151.1
7	lnc-TAF4B-6	chr18:24923216-24923275	ENSG00000264790.1
8	lnc-CHST9-5	chr18:24999586-25000399	NONHSAT058778
9	lnc-CDH2-2	chr18:24916955-24917151	ENSG00000264151.1
10	lnc-CDH2-2	chr18:24918571-24918666	ENSG00000264151.1
11	lnc-CHST9-4	chr18:24935370-24935728	NONHSAT058776
12	lnc-CDH2-2	chr18:24954131-24954211	ENSG00000264151.1
13	lnc-TAF4B-7	chr18:24977916-24977949	ENSG00000263611.1
14	lnc-CDH2-2	chr18:24916343-24917151	ENSG00000264151.1
15	lnc-CHST9-3	chr18:24919252-24919386	l_1548_chr18:24901013-24919386_lung
16	lnc-CHST9-5	chr18:24998848-24999247	NONHSAT058778
17	lnc-TAF4B-6	chr18:24925335-24926074	ENSG00000264790.1
18	lnc-CDH2-2	chr18:24920706-24921095	ENSG00000264151.1
19	lnc-CDH2-2	chr18:24972748-24972831	ENSG00000264151.1
20	lnc-CDH2-2	chr18:24922467-24922648	ENSG00000264151.1

Variant related genes	Relation type
ENSG00000263611	TF binding region
ENSG00000264151	TF binding region
ENSG00000264790	TF binding region
PA2G4P3	TF binding region
RBM22P1	TF binding region
UBA52P9	TF binding region
ENSG00000264790	chromatin interactions
ENSG00000263611	chromatin interactions
ENSG00000264151	chromatin interactions

Extended variants
information (count: 3154 )
Associated
traits (count: 69 )

Variant overlapped rSNPs/rCNVs (count:3154 , 50 per page) page: 1 2 3 4 5 6 7 ... 64

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs562856008	chr18:24913210-24913211	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs9965472	chr18:24913221-24913222	Enhancers	n/a	n/a	Overlapped CNVs	mRNA abundance
3	rs116971753	chr18:24913272-24913273	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs560785437	chr18:24913287-24913288	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs183040809	chr18:24913307-24913308	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs114120587	chr18:24913308-24913309	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs540356802	chr18:24913324-24913325	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs187663322	chr18:24913339-24913340	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs192518638	chr18:24913350-24913351	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs371891483	chr18:24913386-24913387	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs533962002	chr18:24913393-24913394	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs569176831	chr18:24913433-24913434	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs530053324	chr18:24913490-24913491	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs72888043	chr18:24913503-24913504	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs566696173	chr18:24913508-24913509	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs185031986	chr18:24913638-24913639	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs534013188	chr18:24913651-24913652	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs558647000	chr18:24913670-24913671	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs114475527	chr18:24913689-24913690	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs188234248	chr18:24913715-24913716	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs150579119	chr18:24913783-24913784	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs543602134	chr18:24916349-24916350	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
23	rs371021186	chr18:24916358-24916359	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
24	rs2102873	chr18:24916361-24916362	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
25	rs561775166	chr18:24916367-24916368	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
26	rs529374717	chr18:24916371-24916372	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
27	rs190639305	chr18:24916401-24916402	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
28	rs180979634	chr18:24916427-24916428	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
29	rs370231502	chr18:24916452-24916453	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
30	rs533383197	chr18:24916468-24916469	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
31	rs80185373	chr18:24916476-24916477	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
32	rs528068316	chr18:24916488-24916489	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
33	rs570364291	chr18:24916497-24916498	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
34	rs139049612	chr18:24916583-24916584	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
35	rs373079278	chr18:24916629-24916630	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
36	rs59684464	chr18:24916657-24916658	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs113436461	chr18:24916672-24916673	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
38	rs535511432	chr18:24916685-24916686	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
39	rs143186667	chr18:24916695-24916696	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
40	rs569572865	chr18:24916705-24916706	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
41	rs565302667	chr18:24916798-24916799	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
42	rs186154418	chr18:24916816-24916817	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
43	rs557379104	chr18:24916836-24916837	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
44	rs148261989	chr18:24916845-24916846	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
45	rs1607486	chr18:24916886-24916887	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
46	rs191394179	chr18:24916923-24916924	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
47	rs182851211	chr18:24916944-24916945	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
48	rs548790037	chr18:24917001-24917002	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
49	rs541484478	chr18:24917053-24917054	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
50	rs9957698	chr18:24917084-24917085	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:69)

Disease	PMID	Source
Colorectal cancer	16272173	CNVD
Colorectal cancer	19150955	CNVD
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
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
Sudden cardiac death	19188705	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
Acute myeloid leukemia	19651600	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Oral cancer	21386901	CNVD
Colorectal cancer	16912164	CNVD
Renal cell carcinoma	19150565	CNVD
Multiple myeloma	16616336	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:333 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:24913200-24913600	Enhancers	iPS-15b Cell Line	embryonic stem cell
2	chr18:24913200-24913800	Enhancers	ES-I3 Cell Line	embryonic stem cell
3	chr18:24919200-24919400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr18:24919400-24920000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
5	chr18:24919400-24920400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr18:24920000-24920600	Enhancers	Brain Germinal Matrix	brain
7	chr18:24920400-24921200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr18:24925400-24925600	Enhancers	Spleen	Spleen
9	chr18:24932200-24932800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr18:24943400-24944000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr18:24943400-24944000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr18:24944000-24946400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
13	chr18:24945400-24946600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr18:24945600-24946800	Enhancers	Adipose Nuclei	Adipose
15	chr18:24946400-24949000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
16	chr18:24949000-24958200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr18:24950400-24951600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
18	chr18:24953200-24954600	Weak transcription	Psoas Muscle	Psoas
19	chr18:24956400-24959200	Enhancers	HMEC	breast
20	chr18:24956600-24959200	Enhancers	Breast Myoepithelial Primary Cells	Breast
21	chr18:24956800-24959000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
22	chr18:24957000-24957200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr18:24957000-24957800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
24	chr18:24957000-24959000	Enhancers	NH-A	brain
25	chr18:24957200-24957400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr18:24957200-24957400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr18:24957200-24957400	Enhancers	iPS-18 Cell Line	embryonic stem cell
28	chr18:24957200-24957400	Enhancers	Fetal Kidney	kidney
29	chr18:24957200-24959000	Enhancers	ES-I3 Cell Line	embryonic stem cell
30	chr18:24957200-24959000	Enhancers	NHEK	skin
31	chr18:24957200-24959200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
32	chr18:24957200-24959200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
33	chr18:24957200-24959200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
34	chr18:24957400-24958000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
35	chr18:24957400-24958200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr18:24957400-24958400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr18:24957400-24958600	Weak transcription	Fetal Kidney	kidney
38	chr18:24957400-24958800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
39	chr18:24957600-24958800	Enhancers	HUES48 Cell Line	embryonic stem cell
40	chr18:24957800-24958200	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
41	chr18:24957800-24958400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
42	chr18:24957800-24958600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
43	chr18:24957800-24958800	Enhancers	Muscle Satellite Cultured Cells	--
44	chr18:24957800-24959000	Enhancers	Placenta Amnion	Placenta Amnion
45	chr18:24958000-24958800	Enhancers	iPS-18 Cell Line	embryonic stem cell
46	chr18:24958000-24959000	Enhancers	iPS-20b Cell Line	embryonic stem cell
47	chr18:24958200-24959000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
48	chr18:24958200-24959000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
49	chr18:24958200-24959000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
50	chr18:24958200-24959200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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