Variant report

Variant	nsv1033379
Chromosome Location	chr5:116244963-116464338
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1023)
CpG islands
(count:611)
Chromatin interactive
region (count:24)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1023 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:116283657-116283951	HepG2	liver:	n/a	n/a
2	ATF2	chr5:116258221-116258693	GM12878	blood:	n/a	n/a
3	ATF2	chr5:116283512-116283962	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr5:116283643-116284032	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr5:116283536-116283941	GM12878	blood:	n/a	n/a
6	BACH1	chr5:116283620-116284007	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr5:116412789-116413197	H1-hESC	embryonic stem cell:	n/a	n/a
8	BCL11A	chr5:116259165-116259363	H1-hESC	embryonic stem cell:	n/a	n/a
9	BCL11A	chr5:116288970-116289174	H1-hESC	embryonic stem cell:	n/a	n/a
10	BCLAF1	chr5:116258224-116258648	GM12878	blood:	n/a	n/a
11	BCLAF1	chr5:116283526-116284050	GM12878	blood:	n/a	n/a
12	BCLAF1	chr5:116283527-116284066	GM12878	blood:	n/a	n/a
13	BHLHE40	chr5:116274216-116274475	GM12878	blood:	n/a	n/a
14	BHLHE40	chr5:116258273-116258605	GM12878	blood:	n/a	n/a
15	BHLHE40	chr5:116283632-116284071	GM12878	blood:	n/a	n/a
16	BHLHE40	chr5:116431280-116431297	GM12878	blood:	n/a	n/a
17	BHLHE40	chr5:116415297-116415412	GM12878	blood:	n/a	n/a
18	BHLHE40	chr5:116295692-116295698	GM12878	blood:	n/a	n/a
19	BHLHE40	chr5:116432856-116432901	GM12878	blood:	n/a	n/a
20	BRCA1	chr5:116283684-116283936	H1-hESC	embryonic stem cell:	n/a	n/a
21	CCNT2	chr5:116361519-116361714	K562	blood:	n/a	n/a
22	CEBPB	chr5:116279915-116280472	MCF-7	breast:	n/a	chr5:116280152-116280163
23	CEBPB	chr5:116279951-116280323	Hela-S3	cervix:	n/a	chr5:116280152-116280163
24	CEBPB	chr5:116412844-116413184	H1-hESC	embryonic stem cell:	n/a	n/a
25	CEBPB	chr5:116355458-116355994	HepG2	liver:	n/a	n/a
26	CEBPB	chr5:116310220-116310541	HepG2	liver:	n/a	chr5:116310362-116310373
27	CEBPB	chr5:116279852-116280384	MCF-7	breast:	n/a	chr5:116280152-116280163
28	CEBPB	chr5:116278412-116278619	HepG2	liver:	n/a	chr5:116278521-116278532
29	CEBPB	chr5:116355475-116355742	Hela-S3	cervix:	n/a	n/a
30	CEBPB	chr5:116418691-116418876	HepG2	liver:	n/a	chr5:116418729-116418742
31	CEBPB	chr5:116439226-116439346	A549	lung:	n/a	chr5:116439273-116439284 chr5:116439271-116439284 chr5:116439273-116439284
32	CEBPB	chr5:116355462-116355747	A549	lung:	n/a	n/a
33	CEBPB	chr5:116283656-116283951	GM12878	blood:	n/a	n/a
34	CEBPB	chr5:116431280-116431588	HepG2	liver:	n/a	n/a
35	CEBPB	chr5:116290463-116290642	H1-hESC	embryonic stem cell:	n/a	n/a
36	CEBPB	chr5:116284944-116285126	HepG2	liver:	n/a	chr5:116285045-116285056
37	CEBPB	chr5:116412765-116413339	HCT-116	colon:	n/a	n/a
38	CEBPB	chr5:116408435-116408542	H1-hESC	embryonic stem cell:	n/a	n/a
39	CEBPB	chr5:116412840-116413211	MCF-7	breast:	n/a	n/a
40	CEBPB	chr5:116283657-116283974	H1-hESC	embryonic stem cell:	n/a	n/a
41	CEBPB	chr5:116279986-116280313	H1-hESC	embryonic stem cell:	n/a	chr5:116280152-116280163
42	CHD1	chr5:116283643-116283988	GM12878	blood:	n/a	n/a
43	CHD2	chr5:116432777-116433017	GM12878	blood:	n/a	n/a
44	CHD2	chr5:116245168-116245176	GM12878	blood:	n/a	n/a
45	CHD2	chr5:116258321-116258557	GM12878	blood:	n/a	n/a
46	CHD2	chr5:116283506-116284127	H1-hESC	embryonic stem cell:	n/a	n/a
47	CHD2	chr5:116283431-116284028	GM12878	blood:	n/a	n/a
48	CHD2	chr5:116439421-116439555	GM12878	blood:	n/a	n/a
49	CHD2	chr5:116279980-116280241	H1-hESC	embryonic stem cell:	n/a	n/a
50	CHD2	chr5:116274217-116274428	GM12878	blood:	n/a	n/a

(count:611 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:116280275-116280325	BJ	skin:	n/a
2	chr5:116280275-116280325	BJ	skin:	n/a
3	chr5:116385443-116385493	Caco-2	colon:	n/a
4	chr5:116355027-116355077	HL-60	blood:	n/a
5	chr5:116378307-116378357	HCF	heart:	n/a
6	chr5:116274667-116274717	H1-hESC	embryonic stem cell:	embryo
7	chr5:116385300-116385350	AG10803	skin:	n/a
8	chr5:116378307-116378357	SKMC	muscle:	n/a
9	chr5:116289441-116289491	HEEpiC	esophagus:	n/a
10	chr5:116259413-116259463	HL-60	blood:	n/a
11	chr5:116289441-116289491	HCT-116	colon:	n/a
12	chr5:116274667-116274717	HCM	heart:	n/a
13	chr5:116280275-116280325	GM06990	blood:	n/a
14	chr5:116385300-116385350	NHDF-neo	bronchial:	n/a
15	chr5:116274667-116274717	K562	blood:	n/a
16	chr5:116259413-116259463	MCF-7	breast:	n/a
17	chr5:116280275-116280325	LNCaP	prostate:	n/a
18	chr5:116378307-116378357	HAEpiC	amniotic membrane:	n/a
19	chr5:116356275-116356325	SK-N-SH	brain:	n/a
20	chr5:116280275-116280325	HCPEpiC	choroid plexus:	n/a
21	chr5:116378307-116378357	ECC-1	luminal epithelium:	n/a
22	chr5:116280275-116280325	HepG2	liver:	n/a
23	chr5:116378307-116378357	GM12891	blood:	n/a
24	chr5:116274667-116274717	Jurkat	blood:	n/a
25	chr5:116259413-116259463	MCF10A-Er-Src	breast:	n/a
26	chr5:116289441-116289491	HMEC	breast:	n/a
27	chr5:116385300-116385350	GM12892	blood:	n/a
28	chr5:116289441-116289491	A549	lung:	n/a
29	chr5:116356275-116356325	BE2_C	brain:	n/a
30	chr5:116259413-116259463	HRE	kidney:	n/a
31	chr5:116280275-116280325	ProgFib	skin:	n/a
32	chr5:116274667-116274717	MCF10A-Er-Src	breast:	n/a
33	chr5:116378307-116378357	AG09319	gingival:	n/a
34	chr5:116259413-116259463	SK-N-SH	brain:	n/a
35	chr5:116355027-116355077	NHDF-neo	bronchial:	n/a
36	chr5:116280275-116280325	Hepatocyte	liver:	n/a
37	chr5:116385300-116385350	HUVEC	blood vessel:	n/a
38	chr5:116378307-116378357	ovcar-3	ovarian:	n/a
39	chr5:116259413-116259463	HIPEpiC	eye:	n/a
40	chr5:116289441-116289491	GM12892	blood:	n/a
41	chr5:116356275-116356325	Caco-2	colon:	n/a
42	chr5:116306180-116306230	Jurkat	blood:	n/a
43	chr5:116355027-116355077	AG09309	skin:	n/a
44	chr5:116356275-116356325	HRPEpiC	eye:	n/a
45	chr5:116385300-116385350	PrEC	prostate:	n/a
46	chr5:116280275-116280325	HPAEpiC	pulmonary alveolar:	n/a
47	chr5:116280275-116280325	HAEpiC	amniotic membrane:	n/a
48	chr5:116378307-116378357	HEK293	kidney:	embryo
49	chr5:116259413-116259463	SAEC	small airway:	n/a
50	chr5:116356275-116356325	MCF-7	breast:	n/a

(count:24 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:116197562..116200213-chr5:116281914..116283961,2	MCF-7	breast:
2	chr5:116312973..116314849-chr6:26196221..26198277,2	K562	blood:
3	chr4:181060859..181061364-chr5:116353318..116353952,2	MCF-7	breast:
4	chr5:116381480..116384331-chr5:116390056..116392321,2	K562	blood:
5	chr5:116412161..116414057-chr5:116417995..116420455,2	MCF-7	breast:
6	chr5:116381480..116384331-chr5:116390056..116392321,2	K562	blood:
7	chr5:116388114..116390786-chr5:116391482..116393970,2	K562	blood:
8	chr5:116415643..116418388-chr5:116422613..116424563,2	MCF-7	breast:
9	chr5:116403228..116405101-chr5:116405267..116406890,2	K562	blood:
10	chr5:116388114..116390786-chr5:116391482..116393970,2	K562	blood:
11	chr20:49334975..49335937-chr5:116357755..116358651,2	MCF-7	breast:
12	chr5:116370263..116371870-chr5:116372681..116375033,2	K562	blood:
13	chr5:116412161..116414057-chr5:116417995..116420455,2	MCF-7	breast:
14	chr5:116274317..116277091-chr5:116277592..116280132,2	MCF-7	breast:
15	chr5:116360894..116363806-chr5:116375344..116377265,2	MCF-7	breast:
16	chr5:116274317..116277091-chr5:116277592..116280132,2	MCF-7	breast:
17	chr5:116403228..116405101-chr5:116405267..116406890,2	K562	blood:
18	chr5:116415643..116418388-chr5:116422613..116424563,2	MCF-7	breast:
19	chr5:116412565..116413464-chr5:116601306..116602202,3	MCF-7	breast:
20	chr5:116370263..116371870-chr5:116372681..116375033,2	K562	blood:
21	chr5:115473291..115473804-chr5:116283477..116284254,2	MCF-7	breast:
22	chr5:115911257..115912668-chr5:116283296..116284268,6	MCF-7	breast:
23	chr5:116360894..116363806-chr5:116375344..116377265,2	MCF-7	breast:
24	chr5:115911320..115912473-chr5:116283341..116284236,4	MCF-7	breast:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-COMMD10-4	chr5:116366896-116367126	XLOC_004521
2	lnc-COMMD10-11	chr5:116281744-116281873	NONHSAT103381
3	lnc-SEMA6A-8	chr5:116387796-116387856	NONHSAT103384
4	lnc-COMMD10-4	chr5:116374077-116374265	XLOC_004521
5	lnc-COMMD10-11	chr5:116282030-116282143	NONHSAT103381
6	lnc-SEMA6A-8	chr5:116382515-116382695	NONHSAT103384

No data

Variant related genes	Relation type
ENSG00000250650	TF binding region
ENSG00000250949	TF binding region
ENSG00000250650	CpG island
ENSG00000250949	CpG island
ENSG00000197409	chromatin interactions
RBFOX2	miRNA target sites

Extended variants
information (count: 8114 )
Associated
traits (count: 73 )

Variant overlapped rSNPs/rCNVs (count:8114 , 50 per page) page: 1 2 3 4 5 6 7 ... 163

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs557426752	chr5:116244984-116244985	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs113693783	chr5:116245002-116245003	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs577854709	chr5:116245011-116245012	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs532156129	chr5:116245071-116245072	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs182804983	chr5:116245072-116245073	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs574270811	chr5:116245083-116245084	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs113294362	chr5:116245089-116245090	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs543266766	chr5:116245095-116245096	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs149048179	chr5:116245097-116245098	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs565629074	chr5:116245134-116245135	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs74466122	chr5:116245156-116245157	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs545560501	chr5:116245157-116245158	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs565363342	chr5:116245175-116245176	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs200315108	chr5:116245212-116245213	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs533191930	chr5:116245218-116245219	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs111924891	chr5:116245228-116245229	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs148206433	chr5:116245251-116245252	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs188811388	chr5:116245277-116245278	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs549212905	chr5:116245304-116245305	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs568804531	chr5:116245343-116245344	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs537436155	chr5:116245359-116245360	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs192891110	chr5:116245368-116245369	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs563340689	chr5:116245452-116245453	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs370106118	chr5:116245487-116245488	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs13182952	chr5:116245493-116245494	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs185790790	chr5:116245547-116245548	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs116264943	chr5:116245673-116245674	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs142686974	chr5:116245694-116245695	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs113345761	chr5:116245723-116245724	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs112413353	chr5:116245726-116245727	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs712622	chr5:116245737-116245738	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs143654963	chr5:116245775-116245776	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs536715476	chr5:116245777-116245778	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs565252129	chr5:116245791-116245792	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs192367258	chr5:116245793-116245794	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs541495999	chr5:116245806-116245807	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs712623	chr5:116245826-116245827	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs113190559	chr5:116245870-116245871	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs139312221	chr5:116245891-116245892	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs183702215	chr5:116246019-116246020	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs187975531	chr5:116246021-116246022	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs199696186	chr5:116246023-116246024	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs373701708	chr5:116246024-116246025	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs539223644	chr5:116246050-116246051	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs550981928	chr5:116246053-116246054	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs142888042	chr5:116246097-116246098	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs572728163	chr5:116246142-116246143	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs570872036	chr5:116246155-116246156	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs533646691	chr5:116246172-116246173	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs181239219	chr5:116246189-116246190	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:73)

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
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:707 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:116244200-116245000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr5:116244400-116245600	Enhancers	GM12878-XiMat	blood
3	chr5:116245000-116247800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr5:116246400-116247800	Enhancers	Primary T cells from cord blood	blood
5	chr5:116246400-116247800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
6	chr5:116247400-116248600	Enhancers	HSMMtube	muscle
7	chr5:116247800-116248400	Enhancers	Fetal Lung	lung
8	chr5:116248600-116250800	Weak transcription	HSMMtube	muscle
9	chr5:116250200-116251600	Enhancers	Fetal Heart	heart
10	chr5:116250800-116251000	Enhancers	HSMMtube	muscle
11	chr5:116251200-116251400	Enhancers	Left Ventricle	heart
12	chr5:116252200-116252400	Enhancers	H9 Cell Line	embryonic stem cell
13	chr5:116252400-116258800	Weak transcription	H9 Cell Line	embryonic stem cell
14	chr5:116257000-116259400	Enhancers	GM12878-XiMat	blood
15	chr5:116257200-116259200	Enhancers	iPS-20b Cell Line	embryonic stem cell
16	chr5:116257400-116259200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
17	chr5:116258400-116259200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr5:116258400-116260000	Enhancers	HUES64 Cell Line	embryonic stem cell
19	chr5:116258600-116259000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
20	chr5:116258600-116259400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
21	chr5:116258800-116259000	Enhancers	H9 Cell Line	embryonic stem cell
22	chr5:116258800-116259200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr5:116258800-116259200	Enhancers	iPS-15b Cell Line	embryonic stem cell
24	chr5:116258800-116259400	Enhancers	ES-I3 Cell Line	embryonic stem cell
25	chr5:116258800-116259400	Enhancers	HUES6 Cell Line	embryonic stem cell
26	chr5:116258800-116259400	Enhancers	iPS-18 Cell Line	embryonic stem cell
27	chr5:116258800-116259400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
28	chr5:116258800-116259600	Enhancers	HUES48 Cell Line	embryonic stem cell
29	chr5:116259400-116261800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
30	chr5:116263000-116263200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
31	chr5:116266000-116266200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
32	chr5:116266000-116268400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr5:116266400-116268000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
34	chr5:116267400-116269000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
35	chr5:116268000-116269800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
36	chr5:116268400-116274000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr5:116269000-116274000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
38	chr5:116269600-116269800	Enhancers	Fetal Muscle Leg	muscle
39	chr5:116269800-116271000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
40	chr5:116270200-116271400	Weak transcription	Fetal Muscle Leg	muscle
41	chr5:116271400-116271800	Enhancers	Fetal Muscle Leg	muscle
42	chr5:116271400-116273600	Weak transcription	HUES6 Cell Line	embryonic stem cell
43	chr5:116271800-116274200	Weak transcription	Fetal Muscle Leg	muscle
44	chr5:116272400-116272600	Enhancers	ES-I3 Cell Line	embryonic stem cell
45	chr5:116272600-116272800	Flanking Bivalent TSS/Enh	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
46	chr5:116272600-116273400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
47	chr5:116272600-116275600	Enhancers	Right Ventricle	heart
48	chr5:116272800-116273000	ZNF genes & repeats	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
49	chr5:116272800-116273000	Enhancers	H9 Cell Line	embryonic stem cell
50	chr5:116272800-116275600	Enhancers	Left Ventricle	heart

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