Variant report

Variant	nsv462362
Chromosome Location	chr5:104458953-104647213
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:374)
CpG islands
(count:0)
Chromatin interactive
region (count:38)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:374 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:104599139-104599705	K562	blood:	n/a	n/a
2	ARID3A	chr5:104565880-104566023	K562	blood:	n/a	n/a
3	ARID3A	chr5:104574137-104574841	K562	blood:	n/a	n/a
4	ATF1	chr5:104475478-104475496	K562	blood:	n/a	n/a
5	ATF1	chr5:104566225-104566645	K562	blood:	n/a	n/a
6	ATF1	chr5:104599299-104599581	K562	blood:	n/a	n/a
7	BACH1	chr5:104541248-104541265	H1-hESC	embryonic stem cell:	n/a	n/a
8	BCL11A	chr5:104502865-104503067	H1-hESC	embryonic stem cell:	n/a	n/a
9	BRCA1	chr5:104488401-104488414	H1-hESC	embryonic stem cell:	n/a	n/a
10	CCNT2	chr5:104566220-104566624	K562	blood:	n/a	n/a
11	CCNT2	chr5:104599218-104599525	K562	blood:	n/a	n/a
12	CEBPB	chr5:104475581-104475765	H1-hESC	embryonic stem cell:	n/a	n/a
13	CEBPB	chr5:104534357-104534498	HepG2	liver:	n/a	chr5:104534396-104534407
14	CEBPB	chr5:104575874-104575947	HepG2	liver:	n/a	chr5:104575897-104575908 chr5:104575896-104575907
15	CEBPB	chr5:104510149-104510395	H1-hESC	embryonic stem cell:	n/a	chr5:104510228-104510239
16	CEBPB	chr5:104575759-104576055	K562	blood:	n/a	chr5:104575897-104575908 chr5:104575896-104575907
17	CEBPB	chr5:104626968-104627293	HepG2	liver:	n/a	chr5:104627123-104627134
18	CEBPB	chr5:104485759-104485906	H1-hESC	embryonic stem cell:	n/a	n/a
19	CEBPB	chr5:104510170-104510370	K562	blood:	n/a	chr5:104510228-104510239
20	CEBPB	chr5:104475600-104475772	HepG2	liver:	n/a	n/a
21	CEBPB	chr5:104526203-104526286	K562	blood:	n/a	n/a
22	CEBPB	chr5:104475627-104475670	K562	blood:	n/a	n/a
23	CEBPB	chr5:104613163-104613370	HepG2	liver:	n/a	n/a
24	CEBPB	chr5:104593448-104593544	K562	blood:	n/a	chr5:104593456-104593469 chr5:104593456-104593469 chr5:104593458-104593469 chr5:104593456-104593469 chr5:104593458-104593469
25	CEBPB	chr5:104516185-104516507	IMR90	lung:	n/a	n/a
26	CEBPB	chr5:104485721-104485921	K562	blood:	n/a	n/a
27	CEBPB	chr5:104484312-104484512	H1-hESC	embryonic stem cell:	n/a	n/a
28	CEBPB	chr5:104613257-104613341	K562	blood:	n/a	n/a
29	CEBPD	chr5:104566271-104566739	K562	blood:	n/a	n/a
30	CEBPD	chr5:104494206-104494590	K562	blood:	n/a	n/a
31	CHD2	chr5:104502938-104503111	H1-hESC	embryonic stem cell:	n/a	n/a
32	CTCF	chr5:104640660-104640810	HPF	lung:	n/a	n/a
33	CTCF	chr5:104640720-104640870	HRE	kidney:	n/a	n/a
34	CTCF	chr5:104471340-104471490	HEK293	kidney:	n/a	n/a
35	CTCF	chr5:104539330-104539410	Medullo	brain:	n/a	n/a
36	CTCF	chr5:104488600-104488750	BE2_C	brain:	n/a	n/a
37	CTCF	chr5:104640780-104640930	NB4	blood:	n/a	n/a
38	CTCF	chr5:104640640-104640790	HCPEpiC	choroid plexus:	n/a	n/a
39	CTCF	chr5:104579200-104579350	HCM	heart:	n/a	n/a
40	CTCF	chr5:104640740-104640890	GM12865	blood:	n/a	n/a
41	CTCF	chr5:104640660-104640810	Hela-S3	cervix:	n/a	n/a
42	CTCF	chr5:104640620-104640770	MCF-7	breast:	n/a	n/a
43	CTCF	chr5:104471360-104471510	BE2_C	brain:	n/a	n/a
44	CTCF	chr5:104640680-104640830	HBMEC	blood vessel:	n/a	n/a
45	CTCF	chr5:104640700-104640850	HRPEpiC	eye:	n/a	n/a
46	CTCF	chr5:104640640-104640790	HMEC	breast:	n/a	n/a
47	CTCF	chr5:104535035-104535150	Spleen_OC	spleen:	n/a	n/a
48	CTCF	chr5:104570902-104570953	GM20000	blood:	n/a	n/a
49	CTCF	chr5:104506078-104506095	GM10266	blood:	n/a	n/a
50	CTCF	chr5:104640640-104640790	AG04450	lung:	n/a	n/a

No data

(count:38 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:104584886..104590168-chr5:104590478..104594256,4	K562	blood:
2	chr5:104576197..104577737-chr5:104582724..104585208,2	K562	blood:
3	chr5:104482838..104485793-chr5:104489379..104492370,3	MCF-7	breast:
4	chr19:12903711..12905991-chr5:104578289..104580216,2	MCF-7	breast:
5	chr12:23105697..23106553-chr5:104539343..104540254,2	MCF-7	breast:
6	chr5:104567163..104569932-chr5:104572220..104574679,2	MCF-7	breast:
7	chr5:104586940..104589611-chr5:104727738..104729575,2	K562	blood:
8	chr5:104564496..104566595-chr5:104574532..104577348,2	K562	blood:
9	chr5:104604624..104606834-chr5:104613480..104615859,2	K562	blood:
10	chr5:104574990..104577042-chr5:104578460..104580211,2	K562	blood:
11	chr5:104482838..104485793-chr5:104489379..104492370,3	MCF-7	breast:
12	chr5:104512964..104515332-chr5:104570864..104572424,2	K562	blood:
13	chr5:104582906..104584797-chr5:104601356..104603170,2	K562	blood:
14	chr5:104576197..104577737-chr5:104582724..104585208,2	K562	blood:
15	chr5:104528561..104530726-chr5:104532311..104534213,2	K562	blood:
16	chr5:104565194..104566957-chr5:104571048..104573999,2	K562	blood:
17	chr5:104584886..104590168-chr5:104590478..104594256,4	K562	blood:
18	chr5:104540117..104542340-chr5:104543485..104546477,2	MCF-7	breast:
19	chr5:104567163..104569932-chr5:104572220..104574679,2	MCF-7	breast:
20	chr5:104542507..104545042-chr5:104552566..104554250,2	K562	blood:
21	chr5:104545961..104548123-chr5:104549429..104551527,2	K562	blood:
22	chr5:104574990..104577042-chr5:104578460..104580211,2	K562	blood:
23	chr5:104512964..104515332-chr5:104570864..104572424,2	K562	blood:
24	chr5:104565194..104566957-chr5:104571048..104573999,2	K562	blood:
25	chr5:104645770..104648035-chr5:104661663..104663662,2	MCF-7	breast:
26	chr5:104540117..104542340-chr5:104543485..104546477,2	MCF-7	breast:
27	chr5:104604624..104606834-chr5:104613480..104615859,2	K562	blood:
28	chr5:104551002..104553954-chr5:104571477..104574357,2	MCF-7	breast:
29	chr5:104545106..104548123-chr5:104549429..104551527,3	K562	blood:
30	chr5:104564496..104566595-chr5:104574532..104577348,2	K562	blood:
31	chr5:104524711..104526370-chr5:104889242..104892104,2	K562	blood:
32	chr5:104542507..104545042-chr5:104552566..104554250,2	K562	blood:
33	chr5:104545961..104548123-chr5:104549429..104551527,2	K562	blood:
34	chr5:104545106..104548123-chr5:104549429..104551527,3	K562	blood:
35	chr5:104454743..104457659-chr5:104458109..104460411,2	MCF-7	breast:
36	chr5:104528561..104530726-chr5:104532311..104534213,2	K562	blood:
37	chr5:104551002..104553954-chr5:104571477..104574357,2	MCF-7	breast:
38	chr5:104582906..104584797-chr5:104601356..104603170,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NUDT12-7	chr5:104581998-104582065	ENSG00000253584
2	lnc-NUDT12-7	chr5:104582013-104582067	NONHSAT103097

No data

Variant related genes	Relation type
ENSG00000253584	TF binding region
ENSG00000251574	chromatin interactions

Extended variants
information (count: 1977 )
Associated
traits (count: 88 )

Variant overlapped rSNPs/rCNVs (count:1977 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs561996612	chr5:104459643-104459644	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs112839934	chr5:104459773-104459774	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs183620590	chr5:104459777-104459778	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs374154702	chr5:104459809-104459810	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs570477323	chr5:104459829-104459830	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs113904205	chr5:104459918-104459919	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs144732693	chr5:104459924-104459925	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs294151	chr5:104459950-104459951	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs115767407	chr5:104459972-104459973	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs181049994	chr5:104459985-104459986	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs575435940	chr5:104460005-104460006	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs114035053	chr5:104460067-104460068	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs555527134	chr5:104460090-104460091	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs294150	chr5:104460100-104460101	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs185697539	chr5:104460107-104460108	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs557997351	chr5:104460114-104460115	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs577624259	chr5:104460135-104460136	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs554468110	chr5:104460137-104460138	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs189961562	chr5:104460141-104460142	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs543754136	chr5:104460153-104460154	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs140732388	chr5:104460154-104460155	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs143761806	chr5:104460159-104460160	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs294149	chr5:104460160-104460161	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs530989260	chr5:104460176-104460177	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs561885931	chr5:104460180-104460181	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs527448376	chr5:104460193-104460194	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs552623379	chr5:104460198-104460199	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs35372162	chr5:104468251-104468252	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs35874247	chr5:104468276-104468277	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs113282533	chr5:104468286-104468287	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs567672099	chr5:104468303-104468304	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs75324829	chr5:104468333-104468334	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs547160967	chr5:104468399-104468400	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs113486277	chr5:104468401-104468402	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs566841620	chr5:104468406-104468407	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs115212270	chr5:104468435-104468436	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs557647621	chr5:104468519-104468520	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs192639438	chr5:104468548-104468549	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs536964089	chr5:104468577-104468578	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs561983592	chr5:104468583-104468584	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs74355166	chr5:104468627-104468628	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs184485364	chr5:104468632-104468633	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs148408688	chr5:104468637-104468638	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs541049944	chr5:104468662-104468663	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs545058576	chr5:104468668-104468669	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs573978185	chr5:104468692-104468693	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs565351200	chr5:104468730-104468731	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs77453892	chr5:104468752-104468753	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs75935338	chr5:104468762-104468763	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs549768611	chr5:104468794-104468795	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:88)

Disease	PMID	Source
Metanephric adenoma	20802469	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Cancer	16751803	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Breast cancer	17393978	CNVD
Cancer	21359685	CNVD
Non-small cell lung cancer	21829676	CNVD
adenomatous polyposis	22470819	CNVD
Cancer	22429812	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Liposarcoma	21253554	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Breast cancer	21858162	CNVD
Leukemia	17361228	CNVD
Myelodysplastic syndrome	18508791	CNVD
5q-syndrome	17576883	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	16740712	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Urothelial carcinoma	21177765	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
Lung cancer	18438408	CNVD
Retinoblastoma	22278416	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	CNVD
Squamous cell cancer	20885788	CNVD
Hepatocellular carcinoma	16750200	CNVD
Neurodevelopmental disorder	22521361	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	17133270	CNVD
Acute myeloid leukemia	20729466	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	16573809	CNVD
Renal cell carcinoma	18194544	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Cancer	20164920	CNVD
Myelodysplastic syndrome	21251322	CNVD
abnormal development	18461090	CNVD
Colorectal cancer	16774939	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Multiple myeloma	17550852	CNVD
Myelofibrosis	22110671	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Ovarian cancer	21720365	CNVD
Neurocytoma	17123091	CNVD
Salivary gland tumor	18059337	CNVD
Breast cancer	21509527	CNVD
Breast cancer	16608533	CNVD
Obesity	20622171	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Schizophrenia	23813976	CNVD
Lung cancer	16773561	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Schizophrenia	21346763	CNVD

Chromatin state (count:76 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:104459600-104460200	Enhancers	Pancreatic Islets	Pancreatic Islet
2	chr5:104468200-104468800	Enhancers	Brain Germinal Matrix	brain
3	chr5:104469400-104470600	Enhancers	Liver	Liver
4	chr5:104472600-104473200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr5:104473200-104474200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr5:104474200-104474400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr5:104485600-104486600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr5:104486000-104486600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr5:104488800-104489000	Enhancers	Fetal Lung	lung
10	chr5:104489000-104490800	Weak transcription	Fetal Lung	lung
11	chr5:104490800-104491200	ZNF genes & repeats	Fetal Lung	lung
12	chr5:104492600-104492800	ZNF genes & repeats	Aorta	Aorta
13	chr5:104492800-104494200	Weak transcription	Aorta	Aorta
14	chr5:104494000-104495600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
15	chr5:104503600-104504400	Enhancers	HUES48 Cell Line	embryonic stem cell
16	chr5:104503800-104504400	Enhancers	ES-I3 Cell Line	embryonic stem cell
17	chr5:104503800-104504600	Enhancers	iPS-15b Cell Line	embryonic stem cell
18	chr5:104503800-104504600	Enhancers	Hela-S3	cervix
19	chr5:104504400-104505400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
20	chr5:104505800-104506000	Enhancers	ES-I3 Cell Line	embryonic stem cell
21	chr5:104512000-104512400	Active TSS	Breast Myoepithelial Primary Cells	Breast
22	chr5:104541800-104542600	Enhancers	Brain Germinal Matrix	brain
23	chr5:104550000-104550400	Enhancers	HUES48 Cell Line	embryonic stem cell
24	chr5:104550200-104550600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr5:104550200-104550600	Enhancers	HUES6 Cell Line	embryonic stem cell
26	chr5:104550200-104550600	Enhancers	iPS-20b Cell Line	embryonic stem cell
27	chr5:104550200-104550800	Enhancers	ES-I3 Cell Line	embryonic stem cell
28	chr5:104550400-104550600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
29	chr5:104550600-104552600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr5:104550800-104554800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
31	chr5:104552600-104553600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr5:104553000-104553800	Enhancers	Brain Germinal Matrix	brain
33	chr5:104553200-104554200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
34	chr5:104553600-104555200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr5:104554200-104554600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
36	chr5:104554600-104555400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
37	chr5:104554800-104555200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
38	chr5:104555000-104556600	Enhancers	Primary hematopoietic stem cells	blood
39	chr5:104555200-104555400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr5:104555400-104555800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr5:104555800-104557400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr5:104556200-104556600	Active TSS	Primary T helper cells PMA-I stimulated	--
43	chr5:104565200-104565400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr5:104565400-104565800	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr5:104565600-104566600	Enhancers	K562	blood
46	chr5:104565800-104566800	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
47	chr5:104565800-104566800	Enhancers	Colon Smooth Muscle	Colon
48	chr5:104566000-104566400	Enhancers	Primary hematopoietic stem cells short term culture	blood
49	chr5:104566200-104566800	Enhancers	Fetal Lung	lung
50	chr5:104566800-104567600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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