Variant report

Variant	nsv1030281
Chromosome Location	chr5:120300738-120426119
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:267)
CpG islands
(count:61)
Chromatin interactive
region (count:5)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:267 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:120321426-120321583	HepG2	liver:	n/a	n/a
2	BHLHE40	chr5:120355613-120355776	K562	blood:	n/a	n/a
3	CEBPB	chr5:120388756-120389126	Hela-S3	cervix:	n/a	n/a
4	CEBPB	chr5:120313451-120313786	HepG2	liver:	n/a	chr5:120313575-120313586
5	CEBPB	chr5:120313455-120313746	K562	blood:	n/a	chr5:120313575-120313586
6	CEBPB	chr5:120388712-120389167	MCF-7	breast:	n/a	n/a
7	CEBPB	chr5:120321709-120321907	HepG2	liver:	n/a	chr5:120321831-120321842
8	CEBPB	chr5:120409404-120409415	K562	blood:	n/a	n/a
9	CEBPB	chr5:120324365-120324487	K562	blood:	n/a	n/a
10	CEBPB	chr5:120362842-120363162	H1-hESC	embryonic stem cell:	n/a	chr5:120363105-120363118 chr5:120362980-120362991
11	CEBPB	chr5:120362867-120363103	K562	blood:	n/a	chr5:120362980-120362991
12	CEBPB	chr5:120344818-120345134	HepG2	liver:	n/a	n/a
13	CEBPB	chr5:120313457-120313761	A549	lung:	n/a	chr5:120313575-120313586
14	CEBPB	chr5:120325504-120325793	A549	lung:	n/a	chr5:120325601-120325614
15	CEBPB	chr5:120386141-120386392	A549	lung:	n/a	chr5:120386256-120386267
16	CEBPB	chr5:120407480-120407657	HepG2	liver:	n/a	chr5:120407589-120407602
17	CEBPB	chr5:120315991-120316249	HepG2	liver:	n/a	chr5:120316125-120316136
18	CEBPB	chr5:120362859-120363138	HepG2	liver:	n/a	chr5:120363105-120363118 chr5:120362980-120362991
19	CEBPB	chr5:120362833-120363079	IMR90	lung:	n/a	chr5:120362980-120362991
20	CEBPB	chr5:120386100-120386431	HepG2	liver:	n/a	chr5:120386256-120386267
21	CEBPB	chr5:120321723-120321990	HepG2	liver:	n/a	chr5:120321831-120321842
22	CEBPB	chr5:120362854-120363100	A549	lung:	n/a	chr5:120362980-120362991
23	CEBPB	chr5:120382637-120382812	A549	lung:	n/a	chr5:120382770-120382783
24	CEBPB	chr5:120344767-120345102	A549	lung:	n/a	n/a
25	CEBPB	chr5:120344890-120345090	Hela-S3	cervix:	n/a	n/a
26	CTCF	chr5:120324760-120324910	BE2_C	brain:	n/a	n/a
27	CTCF	chr5:120360220-120360370	BE2_C	brain:	n/a	n/a
28	CTCF	chr5:120423520-120423670	GM12868	blood:	n/a	n/a
29	CTCF	chr5:120328935-120328972	GM20000	blood:	n/a	n/a
30	CTCF	chr5:120396480-120396630	GM12875	blood:	n/a	n/a
31	CTCF	chr5:120389160-120389310	BE2_C	brain:	n/a	n/a
32	CTCF	chr5:120367460-120367610	NHDF-neo	bronchial:	n/a	n/a
33	CTCF	chr5:120345376-120345438	GM20000	blood:	n/a	n/a
34	CTCF	chr5:120386313-120386365	Lung_OC	lung:	n/a	n/a
35	CTCF	chr5:120423660-120423810	GM12873	blood:	n/a	n/a
36	CTCF	chr5:120398360-120398510	HVMF	connective:	n/a	n/a
37	E2F4	chr5:120367204-120367277	MCF10A-Er-Src	breast:	n/a	n/a
38	E2F4	chr5:120340284-120340645	MCF10A-Er-Src	breast:	n/a	n/a
39	E2F4	chr5:120363623-120363701	MCF10A-Er-Src	breast:	n/a	n/a
40	E2F4	chr5:120383252-120383370	MCF10A-Er-Src	breast:	n/a	n/a
41	E2F4	chr5:120362573-120362766	MCF10A-Er-Src	breast:	n/a	n/a
42	EBF1	chr5:120363379-120363745	GM12878	blood:	n/a	n/a
43	EBF1	chr5:120358607-120358807	GM12878	blood:	n/a	chr5:120358646-120358657
44	EBF1	chr5:120301258-120301375	GM12878	blood:	n/a	chr5:120301296-120301307
45	EBF1	chr5:120362909-120363050	GM12878	blood:	n/a	n/a
46	EBF1	chr5:120364108-120364112	GM12878	blood:	n/a	n/a
47	ELK1	chr5:120390270-120390366	GM12878	blood:	n/a	n/a
48	EP300	chr5:120388067-120389799	SK-N-SH	brain:	n/a	chr5:120389215-120389229
49	EP300	chr5:120368955-120369384	SK-N-SH_RA	brain:	n/a	n/a
50	EP300	chr5:120327129-120328498	SK-N-SH	brain:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:120400115-120400165	HEEpiC	esophagus:	n/a
2	chr5:120400115-120400165	A549	lung:	n/a
3	chr5:120400115-120400165	HCT-116	colon:	n/a
4	chr5:120400115-120400165	BE2_C	brain:	n/a
5	chr5:120400115-120400165	MCF10A-Er-Src	breast:	n/a
6	chr5:120400115-120400165	T-47D	breast:	n/a
7	chr5:120400115-120400165	HRCEpiC	kidney:	n/a
8	chr5:120400115-120400165	AG09309	skin:	n/a
9	chr5:120400115-120400165	U87	brain:	n/a
10	chr5:120400115-120400165	PANC-1	pancreas:	n/a
11	chr5:120400115-120400165	SKMC	muscle:	n/a
12	chr5:120400115-120400165	HNPCEpiC	eye:	n/a
13	chr5:120400115-120400165	NT2-D1	testis:	n/a
14	chr5:120400115-120400165	GM12892	blood:	n/a
15	chr5:120400115-120400165	ECC-1	luminal epithelium:	n/a
16	chr5:120400115-120400165	HAEpiC	amniotic membrane:	n/a
17	chr5:120400115-120400165	AG09319	gingival:	n/a
18	chr5:120400115-120400165	HepG2	liver:	n/a
19	chr5:120400115-120400165	NB4	blood:	n/a
20	chr5:120400115-120400165	PrEC	prostate:	n/a
21	chr5:120400115-120400165	GM19239	blood:	n/a
22	chr5:120400115-120400165	Caco-2	colon:	n/a
23	chr5:120400115-120400165	RPTEC	kidney:	n/a
24	chr5:120400115-120400165	AG10803	skin:	n/a
25	chr5:120400115-120400165	AG04450	lung:	fetal
26	chr5:120400115-120400165	LNCaP	prostate:	n/a
27	chr5:120400115-120400165	HCM	heart:	n/a
28	chr5:120400115-120400165	HCF	heart:	n/a
29	chr5:120400115-120400165	SK-N-SH	brain:	n/a
30	chr5:120400115-120400165	HRE	kidney:	n/a
31	chr5:120400115-120400165	HL-60	blood:	n/a
32	chr5:120400115-120400165	ovcar-3	ovarian:	n/a
33	chr5:120400115-120400165	K562	blood:	n/a
34	chr5:120400115-120400165	HRPEpiC	eye:	n/a
35	chr5:120400115-120400165	ProgFib	skin:	n/a
36	chr5:120400115-120400165	H1-hESC	embryonic stem cell:	embryo
37	chr5:120400115-120400165	HPAEpiC	pulmonary alveolar:	n/a
38	chr5:120400115-120400165	CMK	blood:	n/a
39	chr5:120400115-120400165	HEK293	kidney:	embryo
40	chr5:120400115-120400165	GM12891	blood:	n/a
41	chr5:120400115-120400165	HMEC	breast:	n/a
42	chr5:120400115-120400165	MCF-7	breast:	n/a
43	chr5:120400115-120400165	NHBE	bronchial:	n/a
44	chr5:120400115-120400165	PFSK-1	brain:	n/a
45	chr5:120400115-120400165	IMR90	lung:	fetal
46	chr5:120400115-120400165	GM12878	blood:	n/a
47	chr5:120400115-120400165	HIPEpiC	eye:	n/a
48	chr5:120400115-120400165	NHDF-neo	bronchial:	n/a
49	chr5:120400115-120400165	SAEC	small airway:	n/a
50	chr5:120400115-120400165	HCPEpiC	choroid plexus:	n/a

(count:5 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:120300949..120302956-chr5:121296548..121298304,2	K562	blood:
2	chr5:120324000..120326925-chr5:120354314..120357069,2	K562	blood:
3	chr5:120324000..120326925-chr5:120354314..120357069,2	K562	blood:
4	chr5:120344504..120347250-chr5:120354364..120356375,2	K562	blood:
5	chr5:120344504..120347250-chr5:120354364..120356375,2	K562	blood:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PRR16-2	chr5:120376385-120376432	NONHSAT103450
2	lnc-PRR16-3	chr5:120396085-120396648	NONHSAT103451
3	lnc-PRR16-2	chr5:120379384-120379727	NONHSAT103450
4	lnc-PRR16-3	chr5:120394939-120395040	NONHSAT103451
5	lnc-PRR16-2	chr5:120375785-120376277	NONHSAT103450

No data

Variant related genes	Relation type
ENSG00000251135	TF binding region
ENSG00000248853	TF binding region
ENSG00000251135	CpG island
ENSG00000248853	CpG island
ENSG00000151304	chromatin interactions

Extended variants
information (count: 3497 )
Associated
traits (count: 74 )

Variant overlapped rSNPs/rCNVs (count:3497 , 50 per page) page: 1 2 3 4 5 6 7 ... 70

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs532426675	chr5:120301000-120301001	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs551036219	chr5:120301052-120301053	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs77184224	chr5:120301075-120301076	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs6867068	chr5:120301076-120301077	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs377242688	chr5:120301181-120301182	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs75249712	chr5:120301235-120301236	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs566741430	chr5:120301249-120301250	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs370496548	chr5:120301289-120301290	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs369856065	chr5:120301348-120301349	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs527954292	chr5:120301394-120301395	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs552480684	chr5:120301401-120301402	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs571207499	chr5:120301432-120301433	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs538296782	chr5:120301481-120301482	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs80133492	chr5:120301487-120301488	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs187608872	chr5:120301503-120301504	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs147963519	chr5:120301519-120301520	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs62382465	chr5:120301527-120301528	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs10038543	chr5:120301554-120301555	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs539725919	chr5:120301579-120301580	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs575247441	chr5:120301588-120301589	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs397884169	chr5:120301594-120301595	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs540511225	chr5:120301634-120301635	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs558925747	chr5:120301664-120301665	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs11241576	chr5:120301681-120301682	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs78058143	chr5:120301701-120301702	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs544234066	chr5:120301717-120301718	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs112269409	chr5:120301740-120301741	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs533368189	chr5:120301766-120301767	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs376014779	chr5:120301773-120301774	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs530105495	chr5:120301774-120301775	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs541942855	chr5:120301832-120301833	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs147039266	chr5:120301866-120301867	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs147655752	chr5:120301888-120301889	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs552444754	chr5:120301944-120301945	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs551522745	chr5:120301974-120301975	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs192566523	chr5:120301991-120301992	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs566642449	chr5:120302008-120302009	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs550265457	chr5:120302043-120302044	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs568848599	chr5:120302058-120302059	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs1157562	chr5:120302074-120302075	Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs554733309	chr5:120302138-120302139	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs566654666	chr5:120302146-120302147	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs185718236	chr5:120302182-120302183	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs190630495	chr5:120302241-120302242	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs181688893	chr5:120302242-120302243	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs370529850	chr5:120302254-120302255	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs556256286	chr5:120302283-120302284	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs544091024	chr5:120302291-120302292	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs549050345	chr5:120302293-120302294	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs574804614	chr5:120302332-120302333	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:74)

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
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
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
Cancer	20164920	CNVD
Myelodysplastic syndrome	21251322	CNVD
Colorectal cancer	16272173	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Multiple myeloma	17550852	CNVD
Ovarian cancer	21720365	CNVD
Salivary gland tumor	18059337	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Renal cell carcinoma	19377443	CNVD
Prostate cancer	16461572	CNVD
Myelofibrosis	22110671	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Glaucoma	21310917	CNVD
Glioblastoma multiforme	22286061	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Renal cell carcinoma	18194544	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:113 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:120302000-120302800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr5:120302600-120302800	ZNF genes & repeats	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr5:120302800-120312200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr5:120316200-120316600	Enhancers	Fetal Brain Male	brain
5	chr5:120321000-120324600	Bivalent Enhancer	Fetal Lung	lung
6	chr5:120324000-120324200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr5:120324200-120324800	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr5:120324200-120325400	Enhancers	Dnd41	blood
9	chr5:120324600-120326200	Enhancers	Fetal Lung	lung
10	chr5:120324800-120325000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr5:120324800-120326600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr5:120325400-120327400	Weak transcription	Dnd41	blood
13	chr5:120326400-120326800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
14	chr5:120326600-120327200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr5:120327000-120327400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr5:120327200-120327400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr5:120327400-120328200	Enhancers	Dnd41	blood
18	chr5:120328200-120334000	Weak transcription	Dnd41	blood
19	chr5:120334000-120334200	Enhancers	Dnd41	blood
20	chr5:120334200-120337600	Weak transcription	Dnd41	blood
21	chr5:120338600-120340600	Enhancers	Dnd41	blood
22	chr5:120340200-120341000	Enhancers	HUVEC	blood vessel
23	chr5:120340600-120343600	Weak transcription	Dnd41	blood
24	chr5:120343600-120345600	Strong transcription	Dnd41	blood
25	chr5:120343800-120345800	Bivalent Enhancer	Fetal Heart	heart
26	chr5:120344400-120344800	Enhancers	Skeletal Muscle Female	skeletal muscle
27	chr5:120345600-120347000	Weak transcription	Dnd41	blood
28	chr5:120347000-120347400	Enhancers	Dnd41	blood
29	chr5:120347400-120348600	Weak transcription	Dnd41	blood
30	chr5:120348600-120348800	Enhancers	Dnd41	blood
31	chr5:120348800-120349000	Genic enhancers	Dnd41	blood
32	chr5:120349000-120350200	Weak transcription	Dnd41	blood
33	chr5:120350200-120351800	Enhancers	Dnd41	blood
34	chr5:120351800-120352200	Active TSS	Dnd41	blood
35	chr5:120352200-120352600	Flanking Active TSS	Dnd41	blood
36	chr5:120352600-120353000	Enhancers	Dnd41	blood
37	chr5:120353000-120355800	Flanking Active TSS	Dnd41	blood
38	chr5:120353400-120353600	Enhancers	HUES48 Cell Line	embryonic stem cell
39	chr5:120353600-120354600	Weak transcription	HUES48 Cell Line	embryonic stem cell
40	chr5:120354600-120355000	Enhancers	HUES48 Cell Line	embryonic stem cell
41	chr5:120354600-120355000	Enhancers	iPS-15b Cell Line	embryonic stem cell
42	chr5:120355800-120357600	Enhancers	Dnd41	blood
43	chr5:120356200-120357600	Bivalent Enhancer	Fetal Lung	lung
44	chr5:120356800-120357600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr5:120357600-120358000	Flanking Bivalent TSS/Enh	Fetal Lung	lung
46	chr5:120357600-120358000	Enhancers	Pancreas	Pancrea
47	chr5:120357600-120358000	Flanking Active TSS	Dnd41	blood
48	chr5:120357800-120358000	Enhancers	Fetal Stomach	stomach
49	chr5:120358000-120358200	Bivalent Enhancer	Fetal Lung	lung
50	chr5:120358000-120358200	Enhancers	Dnd41	blood

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