Variant report

Variant	nsv882464
Chromosome Location	chr5:99784116-99905367
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1125)
CpG islands
(count:976)
Chromatin interactive
region (count:21)
LncRNA
region (count:14)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1125 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr5:99870740-99871206	K562	blood:	n/a	n/a
2	ATF2	chr5:99805499-99805973	GM12878	blood:	n/a	n/a
3	ATF2	chr5:99870603-99871255	GM12878	blood:	n/a	chr5:99870979-99870990
4	ATF2	chr5:99870721-99871127	H1-hESC	embryonic stem cell:	n/a	chr5:99870979-99870990
5	ATF2	chr5:99870739-99871221	GM12878	blood:	n/a	chr5:99870979-99870990
6	ATF2	chr5:99870731-99871119	H1-hESC	embryonic stem cell:	n/a	chr5:99870979-99870990
7	ATF3	chr5:99870861-99871135	K562	blood:	n/a	chr5:99870978-99870988 chr5:99870981-99870989 chr5:99870978-99870988 chr5:99870981-99870988 chr5:99870979-99870990 chr5:99870981-99870992 chr5:99870977-99870992 chr5:99870979-99870990 chr5:99870978-99870991 chr5:99870981-99870991 chr5:99870977-99870990 chr5:99870978-99870989
8	BATF	chr5:99886169-99886390	GM12878	blood:	n/a	n/a
9	BATF	chr5:99805639-99805821	GM12878	blood:	n/a	n/a
10	BATF	chr5:99805585-99805811	GM12878	blood:	n/a	n/a
11	BCL11A	chr5:99805514-99805830	GM12878	blood:	n/a	n/a
12	BCL11A	chr5:99886437-99886629	GM12878	blood:	n/a	n/a
13	BCL11A	chr5:99805489-99805819	GM12878	blood:	n/a	n/a
14	BCLAF1	chr5:99886248-99886772	GM12878	blood:	n/a	n/a
15	BCLAF1	chr5:99870672-99871419	GM12878	blood:	n/a	chr5:99871059-99871068
16	BHLHE40	chr5:99871514-99871882	GM12878	blood:	n/a	n/a
17	BHLHE40	chr5:99870720-99871139	K562	blood:	n/a	n/a
18	BHLHE40	chr5:99805437-99805794	GM12878	blood:	n/a	n/a
19	BRCA1	chr5:99870674-99871232	GM12878	blood:	n/a	n/a
20	BRCA1	chr5:99870828-99871275	HepG2	liver:	n/a	n/a
21	BRCA1	chr5:99869580-99869678	GM12878	blood:	n/a	n/a
22	BRCA1	chr5:99836226-99836426	Hela-S3	cervix:	n/a	n/a
23	BRCA1	chr5:99870679-99871193	Hela-S3	cervix:	n/a	n/a
24	CCNT2	chr5:99871514-99871714	K562	blood:	n/a	n/a
25	CEBPB	chr5:99890906-99891108	IMR90	lung:	n/a	n/a
26	CEBPB	chr5:99784002-99784355	HepG2	liver:	n/a	n/a
27	CEBPB	chr5:99853275-99853404	H1-hESC	embryonic stem cell:	n/a	n/a
28	CEBPB	chr5:99829791-99830035	HepG2	liver:	n/a	chr5:99829921-99829932
29	CEBPB	chr5:99853145-99853522	Hela-S3	cervix:	n/a	n/a
30	CEBPB	chr5:99870650-99871585	Hela-S3	cervix:	n/a	chr5:99870837-99870848
31	CEBPB	chr5:99870900-99871110	K562	blood:	n/a	n/a
32	CEBPB	chr5:99841938-99842358	Hela-S3	cervix:	n/a	n/a
33	CEBPB	chr5:99870850-99871310	HepG2	liver:	n/a	n/a
34	CEBPB	chr5:99898160-99898375	A549	lung:	n/a	n/a
35	CEBPB	chr5:99886551-99886855	IMR90	lung:	n/a	n/a
36	CEBPB	chr5:99784028-99784357	ECC-1	luminal epithelium:	n/a	n/a
37	CEBPB	chr5:99784056-99784276	MCF-7	breast:	n/a	n/a
38	CEBPB	chr5:99784033-99784358	Hela-S3	cervix:	n/a	n/a
39	CEBPB	chr5:99852928-99853520	MCF-7	breast:	n/a	n/a
40	CEBPB	chr5:99891070-99891104	A549	lung:	n/a	n/a
41	CHD1	chr5:99870636-99871628	GM12878	blood:	n/a	n/a
42	CHD2	chr5:99871489-99871707	Hela-S3	cervix:	n/a	n/a
43	CHD2	chr5:99870756-99871267	Hela-S3	cervix:	n/a	n/a
44	CHD2	chr5:99805509-99805751	GM12878	blood:	n/a	n/a
45	CHD2	chr5:99870788-99871395	HepG2	liver:	n/a	n/a
46	CHD2	chr5:99870790-99871249	H1-hESC	embryonic stem cell:	n/a	n/a
47	CHD2	chr5:99870702-99871692	GM12878	blood:	n/a	n/a
48	CREB1	chr5:99870603-99871607	GM12878	blood:	n/a	chr5:99870978-99870991
49	CREB1	chr5:99870714-99871301	K562	blood:	n/a	chr5:99870978-99870991
50	CREB1	chr5:99870702-99871301	H1-hESC	embryonic stem cell:	n/a	chr5:99870978-99870991

(count:976 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:99870887-99870937	SAEC	small airway:	n/a
2	chr5:99869840-99869890	GM12878	blood:	n/a
3	chr5:99871026-99871076	AG04450	lung:	fetal
4	chr5:99871065-99871115	AG04449	skin:	fetal
5	chr5:99870887-99870937	HPAEpiC	pulmonary alveolar:	n/a
6	chr5:99871026-99871076	HAEpiC	amniotic membrane:	n/a
7	chr5:99871073-99871123	NT2-D1	testis:	n/a
8	chr5:99871683-99871733	HMEC	breast:	n/a
9	chr5:99869796-99869846	HCT-116	colon:	n/a
10	chr5:99870955-99871005	NHBE	bronchial:	n/a
11	chr5:99871233-99871283	PFSK-1	brain:	n/a
12	chr5:99871555-99871605	GM19239	blood:	n/a
13	chr5:99870955-99871005	IMR90	lung:	fetal
14	chr5:99870955-99871005	NT2-D1	testis:	n/a
15	chr5:99870957-99871007	K562	blood:	n/a
16	chr5:99871651-99871701	HUVEC	blood vessel:	n/a
17	chr5:99871651-99871701	PrEC	prostate:	n/a
18	chr5:99870957-99871007	PFSK-1	brain:	n/a
19	chr5:99869796-99869846	RPTEC	kidney:	n/a
20	chr5:99875156-99875206	NHDF-neo	bronchial:	n/a
21	chr5:99871073-99871123	HCM	heart:	n/a
22	chr5:99869796-99869846	NB4	blood:	n/a
23	chr5:99871233-99871283	HL-60	blood:	n/a
24	chr5:99871065-99871115	U87	brain:	n/a
25	chr5:99871073-99871123	HCPEpiC	choroid plexus:	n/a
26	chr5:99870955-99871005	NHDF-neo	bronchial:	n/a
27	chr5:99871073-99871123	GM12891	blood:	n/a
28	chr5:99871555-99871605	U87	brain:	n/a
29	chr5:99870957-99871007	HEK293	kidney:	embryo
30	chr5:99870926-99870976	GM06990	blood:	n/a
31	chr5:99870926-99870976	AG04449	skin:	fetal
32	chr5:99869796-99869846	SAEC	small airway:	n/a
33	chr5:99869840-99869890	GM06990	blood:	n/a
34	chr5:99871026-99871076	Caco-2	colon:	n/a
35	chr5:99871683-99871733	BE2_C	brain:	n/a
36	chr5:99871233-99871283	GM12891	blood:	n/a
37	chr5:99871073-99871123	HAEpiC	amniotic membrane:	n/a
38	chr5:99870926-99870976	ProgFib	skin:	n/a
39	chr5:99870887-99870937	HNPCEpiC	eye:	n/a
40	chr5:99871555-99871605	ECC-1	luminal epithelium:	n/a
41	chr5:99871065-99871115	K562	blood:	n/a
42	chr5:99870926-99870976	T-47D	breast:	n/a
43	chr5:99871555-99871605	HNPCEpiC	eye:	n/a
44	chr5:99886768-99886818	K562	blood:	n/a
45	chr5:99871683-99871733	HNPCEpiC	eye:	n/a
46	chr5:99870961-99871011	H1-hESC	embryonic stem cell:	embryo
47	chr5:99871065-99871115	NHDF-neo	bronchial:	n/a
48	chr5:99886768-99886818	RPTEC	kidney:	n/a
49	chr5:99871651-99871701	T-47D	breast:	n/a
50	chr5:99886768-99886818	NH-A	brain:	n/a

(count:21 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:99880455..99883115-chr5:99884041..99887018,2	MCF-7	breast:
2	chr5:99901928..99904752-chr5:99911773..99913756,2	MCF-7	breast:
3	chr5:99871520..99873605-chr5:99874648..99876676,2	MCF-7	breast:
4	chr5:99872854..99874470-chr5:99877624..99879735,2	K562	blood:
5	chr5:99843783..99845513-chr5:99845985..99848114,2	MCF-7	breast:
6	chr5:99813306..99815252-chr5:99818447..99820144,2	K562	blood:
7	chr5:99813306..99815252-chr5:99818447..99820144,2	K562	blood:
8	chr5:99861679..99863597-chr5:99869149..99871005,2	MCF-7	breast:
9	chr2:61371675..61372208-chr5:99870468..99871213,2	NB4	blood:
10	chr5:99843783..99845513-chr5:99845985..99848114,2	MCF-7	breast:
11	chr5:99862444..99865055-chr5:99868858..99871762,2	K562	blood:
12	chr5:99871520..99873605-chr5:99874648..99876676,2	MCF-7	breast:
13	chr5:99814495..99815041-chr5:100726099..100726630,2	MCF-7	breast:
14	chr5:99840638..99843580-chr5:99851710..99854340,2	MCF-7	breast:
15	chr5:99852863..99854851-chr5:99869315..99872165,2	MCF-7	breast:
16	chr16:71322807..71323430-chr5:99870828..99871340,2	Hela-S3	cervix:
17	chr5:99840638..99843580-chr5:99851710..99854340,2	MCF-7	breast:
18	chr5:99872854..99874470-chr5:99877624..99879735,2	K562	blood:
19	chr5:99880455..99883115-chr5:99884041..99887018,2	MCF-7	breast:
20	chr5:99814517..99815454-chr5:100725734..100726727,3	MCF-7	breast:
21	chr5:99870165..99872574-chr5:99872902..99874413,2	MCF-7	breast:

(count:14 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ST8SIA4-3	chr5:99854234-99854315	ENSG00000247877
2	lnc-ST8SIA4-3	chr5:99854234-99854315	NONHSAT103002
3	lnc-ST8SIA4-3	chr5:99869784-99869856	ENSG00000247877
4	lnc-ST8SIA4-3	chr5:99870865-99870966	ENSG00000247877
5	lnc-ST8SIA4-3	chr5:99785458-99786801	NONHSAT103002
6	lnc-ST8SIA4-3	chr5:99869784-99869856	NONHSAT103002
7	lnc-ST8SIA4-3	chr5:99786639-99786801	ENSG00000247877
8	lnc-ST8SIA4-3	chr5:99862010-99862053	NONHSAT103002
9	lnc-ST8SIA4-3	chr5:99854234-99854315	ENSG00000247877
10	lnc-ST8SIA4-3	chr5:99792761-99792828	ENSG00000247877
11	lnc-ST8SIA4-3	chr5:99862010-99862053	ENSG00000247877
12	lnc-ST8SIA4-3	chr5:99869784-99869856	ENSG00000247877
13	lnc-ST8SIA4-3	chr5:99785458-99786801	ENSG00000247877
14	lnc-ST8SIA4-3	chr5:99870865-99870890	ENSG00000247877

No data

Variant related genes	Relation type
FAM174A	TF binding region
ENSG00000247877	TF binding region
FAM174A	CpG island
ENSG00000247877	CpG island
ENSG00000174132	chromatin interactions
ENSG00000212978	chromatin interactions
ENSG00000247877	chromatin interactions
ENSG00000180917	chromatin interactions
HSPC159	miRNA target sites
CLDN12	miRNA target sites
LPGAT1	miRNA target sites
RLF	miRNA target sites
EIF2B1	miRNA target sites
NOTCH2	miRNA target sites
ZBTB38	miRNA target sites
TTLL12	miRNA target sites
FRZB	miRNA target sites

Extended variants
information (count: 2623 )
Associated
traits (count: 89 )

Variant overlapped rSNPs/rCNVs (count:2623 , 50 per page) page: 1 2 3 4 5 6 7 ... 53

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4703100	chr5:99784116-99784117	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs559332239	chr5:99784119-99784120	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs563101610	chr5:99784143-99784144	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs188132613	chr5:99784144-99784145	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs574545931	chr5:99784162-99784163	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs1461634	chr5:99784244-99784245	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs375453219	chr5:99784287-99784288	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs116118035	chr5:99784289-99784290	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs78152964	chr5:99784308-99784309	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs563923169	chr5:99784309-99784310	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs144717973	chr5:99784330-99784331	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs576113870	chr5:99784331-99784332	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs570404003	chr5:99784336-99784337	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs372083081	chr5:99784353-99784354	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs147914583	chr5:99784363-99784364	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs556024918	chr5:99784367-99784368	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs573640365	chr5:99784400-99784401	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs142155528	chr5:99784410-99784411	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs141715603	chr5:99784431-99784432	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs552647370	chr5:99784472-99784473	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs144443643	chr5:99784652-99784653	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs533199970	chr5:99784661-99784662	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs531170745	chr5:99784674-99784675	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs546160706	chr5:99784793-99784794	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs544645148	chr5:99784796-99784797	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs527961653	chr5:99784797-99784798	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs530739310	chr5:99784812-99784813	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs542395750	chr5:99784813-99784814	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs191280002	chr5:99784853-99784854	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs150005071	chr5:99784874-99784875	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs529342909	chr5:99784958-99784959	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs77502367	chr5:99784976-99784977	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs565896897	chr5:99785012-99785013	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs182630458	chr5:99785085-99785086	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs551847104	chr5:99785095-99785096	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs570342578	chr5:99785155-99785156	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs537776868	chr5:99785158-99785159	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs186696038	chr5:99785163-99785164	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs191454424	chr5:99785215-99785216	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs148894809	chr5:99785229-99785230	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs184685197	chr5:99785231-99785232	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs577710206	chr5:99785250-99785251	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs538222519	chr5:99785264-99785265	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs556570915	chr5:99785273-99785274	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs575159569	chr5:99785276-99785277	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs111425644	chr5:99785294-99785295	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs564848614	chr5:99785411-99785412	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs193074214	chr5:99785420-99785421	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs185227703	chr5:99785432-99785433	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs559794652	chr5:99785435-99785436	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:89)

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
Pancreatic ductal adenocarcinoma	19077451	CNVD
Bipolar disorder	19114987	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:857 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:99782600-99786400	Enhancers	Fetal Lung	lung
2	chr5:99783800-99784400	Enhancers	Cortex derived primary cultured neurospheres	brain
3	chr5:99783800-99784600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr5:99790200-99790800	Enhancers	HUVEC	blood vessel
5	chr5:99799600-99800000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr5:99800000-99800600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
7	chr5:99800000-99800600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr5:99800000-99800600	Enhancers	Osteobl	bone
9	chr5:99800600-99801000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
10	chr5:99805400-99805800	Enhancers	Dnd41	blood
11	chr5:99821000-99821800	Enhancers	Fetal Lung	lung
12	chr5:99824200-99824600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr5:99829800-99830200	Enhancers	Fetal Lung	lung
14	chr5:99830200-99830600	Weak transcription	Fetal Lung	lung
15	chr5:99830600-99830800	Enhancers	Fetal Lung	lung
16	chr5:99830800-99832000	Weak transcription	Fetal Lung	lung
17	chr5:99832200-99832400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
18	chr5:99832200-99832400	Enhancers	Fetal Lung	lung
19	chr5:99832400-99835400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
20	chr5:99835400-99835600	ZNF genes & repeats	Foreskin Keratinocyte Primary Cells skin03	Skin
21	chr5:99835600-99841200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
22	chr5:99838200-99841800	Weak transcription	HSMM	muscle
23	chr5:99841200-99842200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
24	chr5:99841200-99842600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
25	chr5:99841200-99842600	Enhancers	Hela-S3	cervix
26	chr5:99841200-99842600	Enhancers	NHEK	skin
27	chr5:99841400-99842400	Enhancers	Fetal Brain Male	brain
28	chr5:99841400-99842400	Enhancers	HMEC	breast
29	chr5:99841400-99842600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
30	chr5:99841400-99842600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
31	chr5:99841400-99842600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
32	chr5:99841600-99842200	Enhancers	Osteobl	bone
33	chr5:99841600-99842400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
34	chr5:99841600-99842600	Enhancers	Muscle Satellite Cultured Cells	--
35	chr5:99841800-99842200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
36	chr5:99841800-99842200	Enhancers	HSMMtube	muscle
37	chr5:99841800-99842200	Enhancers	NH-A	brain
38	chr5:99841800-99842400	Enhancers	Adipose Nuclei	Adipose
39	chr5:99841800-99842400	Enhancers	HSMM	muscle
40	chr5:99841800-99842400	Enhancers	HUVEC	blood vessel
41	chr5:99842000-99842400	Enhancers	HUES64 Cell Line	embryonic stem cell
42	chr5:99842000-99842400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
43	chr5:99842000-99842400	Enhancers	Placenta Amnion	Placenta Amnion
44	chr5:99842000-99842400	Enhancers	A549	lung
45	chr5:99842600-99846800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
46	chr5:99842600-99846800	Weak transcription	NHEK	skin
47	chr5:99846800-99847400	Enhancers	NHEK	skin
48	chr5:99852000-99852200	Enhancers	Dnd41	blood
49	chr5:99852200-99852800	Flanking Active TSS	Dnd41	blood
50	chr5:99852200-99853800	Enhancers	Fetal Muscle Leg	muscle

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