Variant report

Variant	nsv882420
Chromosome Location	chr5:98770145-99183797
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:827)
CpG islands
(count:61)
Chromatin interactive
region (count:16)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:827 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:99057145-99057860	HepG2	liver:	n/a	n/a
2	BATF	chr5:98864846-98865096	GM12878	blood:	n/a	n/a
3	BATF	chr5:98814204-98814519	GM12878	blood:	n/a	n/a
4	BATF	chr5:98814202-98814524	GM12878	blood:	n/a	n/a
5	BCL11A	chr5:98814165-98814533	GM12878	blood:	n/a	n/a
6	BRCA1	chr5:99122610-99122760	H1-hESC	embryonic stem cell:	n/a	n/a
7	BRCA1	chr5:99084107-99084147	HepG2	liver:	n/a	n/a
8	CBX3	chr5:98862548-98862851	K562	blood:	n/a	n/a
9	CCNT2	chr5:98927320-98927465	K562	blood:	n/a	n/a
10	CEBPB	chr5:98922562-98922967	MCF-7	breast:	n/a	n/a
11	CEBPB	chr5:98922755-98922860	HepG2	liver:	n/a	n/a
12	CEBPB	chr5:98986963-98987222	K562	blood:	n/a	chr5:98987138-98987149
13	CEBPB	chr5:98922470-98923076	MCF-7	breast:	n/a	n/a
14	CEBPB	chr5:99144679-99144917	H1-hESC	embryonic stem cell:	n/a	n/a
15	CEBPB	chr5:99144581-99144899	A549	lung:	n/a	n/a
16	CEBPB	chr5:98949487-98949659	IMR90	lung:	n/a	chr5:98949503-98949516
17	CEBPB	chr5:98942379-98942440	HepG2	liver:	n/a	chr5:98942416-98942427
18	CEBPB	chr5:98949448-98949665	A549	lung:	n/a	chr5:98949503-98949516
19	CEBPB	chr5:98862547-98862771	K562	blood:	n/a	n/a
20	CEBPB	chr5:98926512-98927045	MCF-7	breast:	n/a	n/a
21	CEBPB	chr5:98986993-98987297	IMR90	lung:	n/a	chr5:98987138-98987149
22	CEBPB	chr5:99015785-99015940	K562	blood:	n/a	chr5:99015846-99015857
23	CEBPB	chr5:99084164-99084355	HepG2	liver:	n/a	chr5:99084296-99084307
24	CEBPB	chr5:98836275-98836477	HepG2	liver:	n/a	chr5:98836412-98836423 chr5:98836442-98836453
25	CEBPB	chr5:99126521-99126722	H1-hESC	embryonic stem cell:	n/a	n/a
26	CEBPB	chr5:99129266-99129373	H1-hESC	embryonic stem cell:	n/a	n/a
27	CEBPB	chr5:98930693-98930960	HepG2	liver:	n/a	chr5:98930825-98930836
28	CEBPB	chr5:99015733-99015934	A549	lung:	n/a	chr5:99015846-99015857
29	CEBPB	chr5:98986986-98987320	HepG2	liver:	n/a	chr5:98987138-98987149
30	CEBPB	chr5:99144593-99144845	HepG2	liver:	n/a	n/a
31	CEBPB	chr5:98922716-98922875	A549	lung:	n/a	n/a
32	CEBPB	chr5:99038381-99038650	HepG2	liver:	n/a	chr5:99038534-99038545
33	CEBPB	chr5:99122553-99122736	A549	lung:	n/a	n/a
34	CEBPB	chr5:99015709-99015988	HepG2	liver:	n/a	chr5:99015846-99015857
35	CEBPB	chr5:99103187-99103443	A549	lung:	n/a	n/a
36	CEBPB	chr5:98862426-98862864	K562	blood:	n/a	n/a
37	CEBPB	chr5:98949483-98949681	HepG2	liver:	n/a	chr5:98949503-98949516
38	CEBPB	chr5:99011200-99011461	HepG2	liver:	n/a	chr5:99011331-99011342 chr5:99011332-99011341
39	CEBPB	chr5:99116549-99116684	H1-hESC	embryonic stem cell:	n/a	n/a
40	CEBPD	chr5:98862574-98862862	K562	blood:	n/a	n/a
41	CTCF	chr5:99098580-99098730	NB4	blood:	n/a	n/a
42	CTCF	chr5:98982067-98982246	NHEK	skin:	n/a	n/a
43	CTCF	chr5:99051760-99051910	HRPEpiC	eye:	n/a	chr5:99051824-99051840
44	CTCF	chr5:99098752-99098935	MCF-7	breast:	n/a	n/a
45	CTCF	chr5:98982113-98982189	H1-hESC	embryonic stem cell:	n/a	n/a
46	CTCF	chr5:98982090-98982213	Gliobla	brain:	n/a	n/a
47	CTCF	chr5:99095629-99095667	GM20000	blood:	n/a	n/a
48	CTCF	chr5:98853099-98853153	MCF-7	breast:	n/a	n/a
49	CTCF	chr5:98877022-98877089	Medullo	brain:	n/a	n/a
50	CTCF	chr5:99051700-99051850	HCFaa	heart:	n/a	chr5:99051824-99051840

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:98860157-98860207	U87	brain:	n/a
2	chr5:98860157-98860207	HNPCEpiC	eye:	n/a
3	chr5:98860157-98860207	ECC-1	luminal epithelium:	n/a
4	chr5:98860157-98860207	ProgFib	skin:	n/a
5	chr5:98860157-98860207	GM12878	blood:	n/a
6	chr5:98860157-98860207	AG09309	skin:	n/a
7	chr5:98860157-98860207	MCF-7	breast:	n/a
8	chr5:98860157-98860207	HAEpiC	amniotic membrane:	n/a
9	chr5:98860157-98860207	HRPEpiC	eye:	n/a
10	chr5:98860157-98860207	LNCaP	prostate:	n/a
11	chr5:98860157-98860207	ovcar-3	ovarian:	n/a
12	chr5:98860157-98860207	Caco-2	colon:	n/a
13	chr5:98860157-98860207	RPTEC	kidney:	n/a
14	chr5:98860157-98860207	A549	lung:	n/a
15	chr5:98860157-98860207	HRE	kidney:	n/a
16	chr5:98860157-98860207	T-47D	breast:	n/a
17	chr5:98860157-98860207	PFSK-1	brain:	n/a
18	chr5:98860157-98860207	K562	blood:	n/a
19	chr5:98860157-98860207	HEK293	kidney:	embryo
20	chr5:98860157-98860207	MCF10A-Er-Src	breast:	n/a
21	chr5:98860157-98860207	Hepatocyte	liver:	n/a
22	chr5:98860157-98860207	CMK	blood:	n/a
23	chr5:98860157-98860207	GM12892	blood:	n/a
24	chr5:98860157-98860207	NB4	blood:	n/a
25	chr5:98860157-98860207	NT2-D1	testis:	n/a
26	chr5:98860157-98860207	HL-60	blood:	n/a
27	chr5:98860157-98860207	H1-hESC	embryonic stem cell:	embryo
28	chr5:98860157-98860207	HCM	heart:	n/a
29	chr5:98860157-98860207	HEEpiC	esophagus:	n/a
30	chr5:98860157-98860207	HCT-116	colon:	n/a
31	chr5:98860157-98860207	AG09319	gingival:	n/a
32	chr5:98860157-98860207	GM19239	blood:	n/a
33	chr5:98860157-98860207	HRCEpiC	kidney:	n/a
34	chr5:98860157-98860207	NH-A	brain:	n/a
35	chr5:98860157-98860207	AG04449	skin:	fetal
36	chr5:98860157-98860207	PANC-1	pancreas:	n/a
37	chr5:98860157-98860207	HepG2	liver:	n/a
38	chr5:98860157-98860207	NHBE	bronchial:	n/a
39	chr5:98860157-98860207	HCF	heart:	n/a
40	chr5:98860157-98860207	Hela-S3	cervix:	n/a
41	chr5:98860157-98860207	HUVEC	blood vessel:	n/a
42	chr5:98860157-98860207	NHDF-neo	bronchial:	n/a
43	chr5:98860157-98860207	HMEC	breast:	n/a
44	chr5:98860157-98860207	GM12891	blood:	n/a
45	chr5:98860157-98860207	SAEC	small airway:	n/a
46	chr5:98860157-98860207	HPAEpiC	pulmonary alveolar:	n/a
47	chr5:98860157-98860207	SKMC	muscle:	n/a
48	chr5:98860157-98860207	AG10803	skin:	n/a
49	chr5:98860157-98860207	SK-N-SH	brain:	n/a
50	chr5:98860157-98860207	HCPEpiC	choroid plexus:	n/a

(count:16 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:98936687..98938908-chr5:98939757..98941511,2	MCF-7	breast:
2	chr5:98973640..98976479-chr5:98981401..98983390,2	MCF-7	breast:
3	chr5:99141699..99143792-chr5:99151090..99154054,2	MCF-7	breast:
4	chr5:99089940..99092003-chr5:99110491..99113397,2	MCF-7	breast:
5	chr5:99141699..99143792-chr5:99151090..99154054,2	MCF-7	breast:
6	chr5:98973640..98976479-chr5:98981401..98983390,2	MCF-7	breast:
7	chr5:99014412..99016178-chr5:99017039..99019212,2	K562	blood:
8	chr5:98983247..98985665-chr5:98986689..98988477,2	K562	blood:
9	chr5:98936687..98938908-chr5:98939757..98941511,2	MCF-7	breast:
10	chr5:99100175..99102793-chr5:99107234..99109956,2	MCF-7	breast:
11	chr5:99014412..99016178-chr5:99017039..99019212,2	K562	blood:
12	chr5:99100175..99102793-chr5:99107234..99109956,2	MCF-7	breast:
13	chr5:99005599..99009743-chr5:99010276..99013460,3	MCF-7	breast:
14	chr5:99005599..99009743-chr5:99010276..99013460,3	MCF-7	breast:
15	chr5:98983247..98985665-chr5:98986689..98988477,2	K562	blood:
16	chr5:99089940..99092003-chr5:99110491..99113397,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RGMB-8	chr5:98825263-98825644	NONHSAT102979
2	lnc-CHD1-8	chr5:98930033-98930444	NONHSAT102982
3	lnc-RGMB-2	chr5:98913427-98913661	ENSG00000249515
4	lnc-RGMB-2	chr5:98885136-98885236	ENSG00000249515
5	lnc-RGMB-9	chr5:98930584-98931001	NONHSAT102983
6	lnc-RGMB-8	chr5:98834774-98835071	NONHSAT102979

No data

Variant related genes	Relation type
ENSG00000249444	TF binding region
ENSG00000248928	TF binding region
ENSG00000249515	TF binding region
ENSG00000206356	TF binding region
ENSG00000248236	TF binding region
GUSBP8	TF binding region
ENSG00000249444	CpG island
ENSG00000248928	CpG island
ENSG00000249515	CpG island
ENSG00000206356	CpG island
ENSG00000248236	CpG island
GUSBP8	CpG island

Extended variants
information (count: 3159 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:3159 , 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	rs2688944	chr5:98770145-98770146	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs148328799	chr5:98770149-98770150	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs373674958	chr5:98770150-98770151	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs562492431	chr5:98770161-98770162	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs57343226	chr5:98770172-98770173	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs550868350	chr5:98770182-98770183	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs2963575	chr5:98773004-98773005	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs187893648	chr5:98773018-98773019	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs541064541	chr5:98773019-98773020	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs35952439	chr5:98773044-98773045	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs9326792	chr5:98773051-98773052	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs531226740	chr5:98773056-98773057	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs112476917	chr5:98773065-98773066	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs544006485	chr5:98773067-98773068	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs549885435	chr5:98773094-98773095	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs556013772	chr5:98773097-98773098	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs561604068	chr5:98773117-98773118	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs528926544	chr5:98773140-98773141	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs149742267	chr5:98773142-98773143	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs182995670	chr5:98773150-98773151	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs565636747	chr5:98773154-98773155	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs187378877	chr5:98773161-98773162	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs543484989	chr5:98773196-98773197	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs570280385	chr5:98773225-98773226	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs192591707	chr5:98773268-98773269	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs555876441	chr5:98773313-98773314	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs376746513	chr5:98773357-98773358	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs79965816	chr5:98773391-98773392	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs576854188	chr5:98773408-98773409	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs552951466	chr5:98773427-98773428	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs545531496	chr5:98773532-98773533	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs140916977	chr5:98773546-98773547	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs559121718	chr5:98773595-98773596	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs545705214	chr5:98773625-98773626	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs150198444	chr5:98773658-98773659	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs1523381	chr5:98773754-98773755	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs544937046	chr5:98773790-98773791	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs73143525	chr5:98773828-98773829	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs118175841	chr5:98773830-98773831	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs547469740	chr5:98773873-98773874	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs139091954	chr5:98773877-98773878	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs185427963	chr5:98773903-98773904	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs559413776	chr5:98773915-98773916	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs116462319	chr5:98773918-98773919	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs552137960	chr5:98773922-98773923	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs7705126	chr5:98773928-98773929	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs192244176	chr5:98773931-98773932	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs34458728	chr5:98774003-98774004	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs11241054	chr5:98774009-98774010	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs570792622	chr5:98774027-98774028	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:87)

Disease	PMID	Source
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
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
Merkel cell carcinoma	19020549	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
Testicular cancer	18059402	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
Myelofibrosis	22110671	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
Glioblastoma multiforme	22286061	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Ovarian cancer	21720365	CNVD
Prostate cancer	16461572	CNVD
Neurocytoma	17123091	CNVD
Salivary gland tumor	18059337	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:138 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:98767600-98770200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr5:98773000-98773600	Enhancers	Colon Smooth Muscle	Colon
3	chr5:98773200-98774000	Enhancers	Fetal Kidney	kidney
4	chr5:98773400-98774200	Enhancers	Rectal Smooth Muscle	rectum
5	chr5:98773600-98773800	Enhancers	Gastric	stomach
6	chr5:98779000-98779400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr5:98779000-98779800	Enhancers	Stomach Mucosa	stomach
8	chr5:98779800-98780800	Weak transcription	Stomach Mucosa	stomach
9	chr5:98780800-98781800	Enhancers	Stomach Mucosa	stomach
10	chr5:98781200-98781600	Enhancers	Gastric	stomach
11	chr5:98781800-98783600	Weak transcription	Stomach Mucosa	stomach
12	chr5:98783600-98784000	Enhancers	Stomach Mucosa	stomach
13	chr5:98785400-98785800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
14	chr5:98785400-98786000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr5:98795600-98796800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr5:98795600-98798000	Enhancers	HUVEC	blood vessel
17	chr5:98795800-98796200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
18	chr5:98796000-98796400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
19	chr5:98796000-98796400	Enhancers	HMEC	breast
20	chr5:98796200-98796600	Enhancers	Stomach Mucosa	stomach
21	chr5:98797800-98798000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
22	chr5:98829400-98830400	Enhancers	HUES48 Cell Line	embryonic stem cell
23	chr5:98830000-98830400	Enhancers	HUES64 Cell Line	embryonic stem cell
24	chr5:98830000-98830400	Enhancers	iPS-20b Cell Line	embryonic stem cell
25	chr5:98858000-98858400	Enhancers	Fetal Muscle Trunk	muscle
26	chr5:98858000-98858400	Enhancers	Fetal Muscle Leg	muscle
27	chr5:98858400-98859400	Weak transcription	Fetal Muscle Trunk	muscle
28	chr5:98859400-98859600	Enhancers	Fetal Muscle Trunk	muscle
29	chr5:98870000-98870200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
30	chr5:98877000-98877200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr5:98877400-98879000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr5:98878800-98879000	Enhancers	HSMMtube	muscle
33	chr5:98878800-98879800	Enhancers	Fetal Lung	lung
34	chr5:98879000-98880000	Weak transcription	HSMMtube	muscle
35	chr5:98879000-98880400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr5:98879200-98880200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
37	chr5:98879200-98880400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
38	chr5:98879800-98880200	Enhancers	Placenta Amnion	Placenta Amnion
39	chr5:98880000-98880600	Enhancers	HSMMtube	muscle
40	chr5:98885000-98885600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr5:98898800-98899400	Active TSS	HUES6 Cell Line	embryonic stem cell
42	chr5:98914400-98915200	Enhancers	HUVEC	blood vessel
43	chr5:98914600-98915200	Enhancers	Fetal Heart	heart
44	chr5:98915200-98916400	Weak transcription	HUVEC	blood vessel
45	chr5:98915200-98930800	Weak transcription	Fetal Heart	heart
46	chr5:98916400-98917800	Enhancers	HUVEC	blood vessel
47	chr5:98917800-98919000	Weak transcription	HUVEC	blood vessel
48	chr5:98919000-98919600	Enhancers	HUVEC	blood vessel
49	chr5:98922200-98923000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
50	chr5:98922800-98923400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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