Variant report

Variant	nsv1033278
Chromosome Location	chr5:103383207-103773361
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1724)
CpG islands
(count:0)
Chromatin interactive
region (count:100)
LncRNA
region (count:13)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1724 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:103533944-103534020	HepG2	liver:	n/a	n/a
2	ARID3A	chr5:103424586-103425489	K562	blood:	n/a	n/a
3	ARID3A	chr5:103388967-103389033	K562	blood:	n/a	n/a
4	ATF1	chr5:103424670-103425482	K562	blood:	n/a	n/a
5	ATF1	chr5:103525691-103525882	K562	blood:	n/a	n/a
6	ATF1	chr5:103582934-103583199	K562	blood:	n/a	n/a
7	ATF1	chr5:103427458-103427492	K562	blood:	n/a	n/a
8	ATF3	chr5:103425143-103425446	K562	blood:	n/a	n/a
9	ATF3	chr5:103525596-103526013	K562	blood:	n/a	chr5:103525833-103525847
10	BACH1	chr5:103420138-103420206	K562	blood:	n/a	n/a
11	BACH1	chr5:103425247-103425428	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr5:103424849-103425597	K562	blood:	n/a	n/a
13	BATF	chr5:103425050-103425493	GM12878	blood:	n/a	chr5:103425282-103425293
14	BATF	chr5:103400582-103400825	GM12878	blood:	n/a	n/a
15	BATF	chr5:103425096-103425463	GM12878	blood:	n/a	chr5:103425282-103425293
16	BCL11A	chr5:103425108-103425491	GM12878	blood:	n/a	chr5:103425281-103425290 chr5:103425282-103425291
17	BCL11A	chr5:103425087-103425461	GM12878	blood:	n/a	chr5:103425281-103425290 chr5:103425282-103425291
18	BCL3	chr5:103524584-103524828	GM12878	blood:	n/a	n/a
19	BHLHE40	chr5:103691018-103691342	HepG2	liver:	n/a	n/a
20	BHLHE40	chr5:103424858-103425183	K562	blood:	n/a	n/a
21	BHLHE40	chr5:103525586-103525928	K562	blood:	n/a	n/a
22	BHLHE40	chr5:103521859-103522065	K562	blood:	n/a	n/a
23	BHLHE40	chr5:103533950-103534025	HepG2	liver:	n/a	n/a
24	BRCA1	chr5:103681266-103681273	Hela-S3	cervix:	n/a	n/a
25	BRCA1	chr5:103514840-103515343	Hela-S3	cervix:	n/a	n/a
26	BRCA1	chr5:103508218-103508346	Hela-S3	cervix:	n/a	n/a
27	CBX3	chr5:103525630-103525950	K562	blood:	n/a	n/a
28	CBX3	chr5:103424834-103425657	HCT-116	colon:	n/a	n/a
29	CBX3	chr5:103521731-103522132	HCT-116	colon:	n/a	n/a
30	CBX3	chr5:103521726-103522181	K562	blood:	n/a	n/a
31	CBX3	chr5:103525245-103525937	K562	blood:	n/a	n/a
32	CBX3	chr5:103424562-103425521	K562	blood:	n/a	n/a
33	CBX3	chr5:103469878-103470276	K562	blood:	n/a	n/a
34	CBX3	chr5:103440319-103440817	K562	blood:	n/a	n/a
35	CBX3	chr5:103524709-103525168	K562	blood:	n/a	n/a
36	CBX3	chr5:103521811-103522125	K562	blood:	n/a	n/a
37	CCNT2	chr5:103424875-103425443	K562	blood:	n/a	n/a
38	CCNT2	chr5:103526459-103526708	K562	blood:	n/a	n/a
39	CEBPB	chr5:103396717-103396915	A549	lung:	n/a	chr5:103396855-103396866
40	CEBPB	chr5:103689205-103689554	HepG2	liver:	n/a	n/a
41	CEBPB	chr5:103499677-103499895	HepG2	liver:	n/a	n/a
42	CEBPB	chr5:103447273-103447500	A549	lung:	n/a	chr5:103447373-103447386
43	CEBPB	chr5:103427036-103427225	A549	lung:	n/a	chr5:103427132-103427145 chr5:103427134-103427143 chr5:103427134-103427143 chr5:103427132-103427145 chr5:103427132-103427145 chr5:103427132-103427143 chr5:103427142-103427154 chr5:103427133-103427144 chr5:103427134-103427143 chr5:103427132-103427143 chr5:103427134-103427143
44	CEBPB	chr5:103680587-103680866	A549	lung:	n/a	chr5:103680714-103680725
45	CEBPB	chr5:103406326-103406633	IMR90	lung:	n/a	n/a
46	CEBPB	chr5:103464090-103464423	H1-hESC	embryonic stem cell:	n/a	chr5:103464254-103464263 chr5:103464252-103464265 chr5:103464254-103464263 chr5:103464254-103464263
47	CEBPB	chr5:103720632-103720781	K562	blood:	n/a	chr5:103720741-103720752
48	CEBPB	chr5:103464069-103464420	Hela-S3	cervix:	n/a	chr5:103464254-103464263 chr5:103464252-103464265 chr5:103464254-103464263 chr5:103464254-103464263
49	CEBPB	chr5:103521808-103522127	K562	blood:	n/a	chr5:103521977-103521988
50	CEBPB	chr5:103424808-103425495	K562	blood:	n/a	chr5:103425288-103425299

No data

(count:100 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr5:103424304..103427061-chr5:103434256..103435929,2	K562	blood:
2	chr5:103574324..103576071-chr5:103577725..103579233,2	K562	blood:
3	chr5:103755525..103757594-chr5:103760680..103762734,2	K562	blood:
4	chr5:103630146..103633049-chr5:103637946..103640879,3	K562	blood:
5	chr5:103406028..103408953-chr5:103419618..103421464,2	K562	blood:
6	chr5:103633936..103636203-chr5:103642524..103644574,2	K562	blood:
7	chr5:103677480..103679978-chr5:103685994..103688346,2	K562	blood:
8	chr5:103547602..103549522-chr5:103555358..103558237,2	K562	blood:
9	chr5:103467212..103468815-chr5:103480734..103482743,2	K562	blood:
10	chr5:103580298..103582448-chr5:103583760..103585414,2	MCF-7	breast:
11	chr5:75897144..75897771-chr5:103707251..103707772,2	MCF-7	breast:
12	chr5:103424892..103429270-chr5:103431386..103433912,4	K562	blood:
13	chr5:103504487..103508742-chr5:103509430..103512265,3	K562	blood:
14	chr5:103500874..103502954-chr5:103505978..103507826,2	K562	blood:
15	chr5:103541472..103544045-chr5:103667629..103669884,2	K562	blood:
16	chr12:112035976..112038316-chr5:103433179..103435078,2	MCF-7	breast:
17	chr5:103440945..103442591-chr5:103463038..103465422,2	K562	blood:
18	chr5:103579485..103581978-chr5:103587465..103589014,2	MCF-7	breast:
19	chr5:103579485..103581978-chr5:103587465..103589014,2	MCF-7	breast:
20	chr5:103440945..103442591-chr5:103463038..103465422,2	K562	blood:
21	chr5:103581733..103583397-chr5:103587148..103588917,2	MCF-7	breast:
22	chr5:103575723..103577605-chr5:103642604..103644571,2	K562	blood:
23	chr5:103541472..103544045-chr5:103667629..103669884,2	K562	blood:
24	chr5:103488217..103490726-chr5:103523272..103524966,2	K562	blood:
25	chr5:103630146..103633049-chr5:103637946..103640879,3	K562	blood:
26	chr5:103424892..103427295-chr5:103431386..103434334,3	K562	blood:
27	chr5:103445190..103447987-chr5:103454013..103455945,2	K562	blood:
28	chr5:103431462..103433805-chr5:103436805..103438651,2	K562	blood:
29	chr5:103472133..103474624-chr5:103476667..103479218,2	K562	blood:
30	chr5:103519669..103522372-chr5:103523463..103525716,2	K562	blood:
31	chr5:103747998..103750504-chr5:103755568..103757533,2	MCF-7	breast:
32	chr5:103598709..103601053-chr5:103607200..103608906,2	K562	blood:
33	chr5:103568513..103570154-chr5:103579261..103581624,2	K562	blood:
34	chr5:103575723..103577605-chr5:103642604..103644571,2	K562	blood:
35	chr5:103249220..103251663-chr5:103417841..103420142,2	K562	blood:
36	chr5:103598709..103601053-chr5:103607200..103608906,2	K562	blood:
37	chr5:103419555..103422324-chr5:103423618..103426898,4	K562	blood:
38	chr5:103424892..103427295-chr5:103431386..103434334,3	K562	blood:
39	chr5:103469361..103471032-chr5:103473793..103476182,2	K562	blood:
40	chr5:103380875..103382995-chr5:103388672..103391460,2	MCF-7	breast:
41	chr5:103720063..103721767-chr5:103728887..103730529,2	MCF-7	breast:
42	chr5:103614351..103617259-chr5:103627051..103629322,2	K562	blood:
43	chr5:103144212..103144806-chr5:103748305..103749025,2	MCF-7	breast:
44	chr5:103755525..103757594-chr5:103760680..103762734,2	K562	blood:
45	chr5:103530400..103532599-chr5:103544330..103547134,2	K562	blood:
46	chr15:100541763..100542576-chr5:103512576..103513415,2	MCF-7	breast:
47	chr5:103493121..103495084-chr5:103495998..103498553,2	K562	blood:
48	chr5:103457491..103460470-chr5:103461243..103465378,4	K562	blood:
49	chr5:44578647..44579149-chr5:103415633..103416333,2	Hela-S3	cervix:
50	chr5:103432374..103435053-chr5:103436419..103438700,3	MCF-7	breast:

(count:13 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C5orf30-7	chr5:103404720-103405076	NONHSAT103072
2	lnc-C5orf30-1	chr5:103415612-103415825	ENSG00000251026
3	lnc-C5orf30-1	chr5:103417581-103417648	ENSG00000251026
4	lnc-C5orf30-7	chr5:103402464-103402570	NONHSAT103072
5	lnc-NUDT12-6	chr5:103718999-103719083	ENSG00000251574
6	lnc-NUDT12-4	chr5:103716257-103716480	XLOC_004946
7	lnc-C5orf30-1	chr5:103441061-103441104	ENSG00000251026
8	lnc-NUDT12-4	chr5:103716610-103716740	XLOC_004946
9	lnc-C5orf30-1	chr5:103439963-103439988	NONHSAT147352
10	lnc-C5orf30-1	chr5:103416609-103416742	ENSG00000251026
11	lnc-C5orf30-1	chr5:103441061-103443042	NONHSAT147352
12	lnc-NUDT12-12	chr5:103596234-103596527	NONHSAT103075
13	lnc-C5orf30-1	chr5:103439875-103439988	ENSG00000251026

No data

Variant related genes	Relation type
ENSG00000251026	TF binding region
RNU1-140P	TF binding region
RN7SL255P	TF binding region
ENSG00000201910	chromatin interactions
ENSG00000251026	chromatin interactions
ENSG00000181751	chromatin interactions
ENSG00000258099	chromatin interactions
ENSG00000118900	chromatin interactions
ENSG00000140632	chromatin interactions
ENSG00000204842	chromatin interactions

Extended variants
information (count: 6926 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:6926 , 50 per page) page: 1 2 3 4 5 6 7 ... 139

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs372887258	chr5:103383243-103383244	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs115697538	chr5:103383297-103383298	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs571850652	chr5:103383318-103383319	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs60372355	chr5:103383344-103383345	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs368429738	chr5:103383379-103383380	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs563897780	chr5:103383432-103383433	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs111790248	chr5:103383462-103383463	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs184125661	chr5:103383489-103383490	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs190676988	chr5:103383539-103383540	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs563627227	chr5:103383550-103383551	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs529095771	chr5:103383601-103383602	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs73196587	chr5:103383602-103383603	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs565887632	chr5:103383609-103383610	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs535075339	chr5:103383683-103383684	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs551875388	chr5:103383687-103383688	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs147614100	chr5:103383722-103383723	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs537488336	chr5:103383804-103383805	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs557350270	chr5:103383902-103383903	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs574042953	chr5:103383923-103383924	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs74926553	chr5:103383947-103383948	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs558698452	chr5:103383977-103383978	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs142120881	chr5:103384010-103384011	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs573123105	chr5:103384067-103384068	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs577687364	chr5:103384077-103384078	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs540733761	chr5:103384078-103384079	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs564240475	chr5:103384123-103384124	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs62363589	chr5:103384149-103384150	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs76741800	chr5:103384154-103384155	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs192490126	chr5:103384179-103384180	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs144527121	chr5:103384182-103384183	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs529158774	chr5:103384184-103384185	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs111705944	chr5:103384185-103384186	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs147840933	chr5:103384230-103384231	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs549303691	chr5:103384238-103384239	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs535888339	chr5:103384286-103384287	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs75203702	chr5:103384306-103384307	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs528313095	chr5:103384315-103384316	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs551571107	chr5:103384350-103384351	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs200066396	chr5:103384351-103384352	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs571742129	chr5:103384358-103384359	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs537048218	chr5:103384363-103384364	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs550993596	chr5:103384369-103384370	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs73775513	chr5:103384439-103384440	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs372452127	chr5:103384467-103384468	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs184715799	chr5:103384492-103384493	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs116460519	chr5:103384522-103384523	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs369369829	chr5:103384534-103384535	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs557563604	chr5:103384574-103384575	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs1420863	chr5:103384621-103384622	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs4703023	chr5:103384685-103384686	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:83)

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
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Schizophrenia	23813976	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:406 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:103382000-103385600	Weak transcription	Ovary	ovary
2	chr5:103382200-103383800	Weak transcription	Fetal Lung	lung
3	chr5:103383800-103384000	Enhancers	Fetal Lung	lung
4	chr5:103383800-103384000	Enhancers	Osteobl	bone
5	chr5:103383800-103384600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
6	chr5:103384000-103384400	Weak transcription	Fetal Lung	lung
7	chr5:103384000-103384600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
8	chr5:103384400-103384600	Enhancers	Fetal Lung	lung
9	chr5:103384600-103385800	Weak transcription	Fetal Lung	lung
10	chr5:103385600-103386200	Enhancers	Ovary	ovary
11	chr5:103385800-103387000	Enhancers	Fetal Lung	lung
12	chr5:103386200-103386800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
13	chr5:103386200-103386800	Weak transcription	Ovary	ovary
14	chr5:103386800-103387000	Enhancers	Ovary	ovary
15	chr5:103386800-103388800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
16	chr5:103388400-103388600	Enhancers	Brain Cingulate Gyrus	brain
17	chr5:103388800-103389000	Enhancers	Fetal Lung	lung
18	chr5:103388800-103389200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
19	chr5:103388800-103389200	Enhancers	Colon Smooth Muscle	Colon
20	chr5:103395600-103397000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr5:103396800-103397200	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
22	chr5:103397200-103402000	Weak transcription	HUES48 Cell Line	embryonic stem cell
23	chr5:103397800-103398400	Enhancers	iPS-15b Cell Line	embryonic stem cell
24	chr5:103398400-103398600	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
25	chr5:103398400-103398800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr5:103398400-103398800	Active TSS	Rectal Mucosa Donor 29	rectum
27	chr5:103398400-103404000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
28	chr5:103398600-103398800	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
29	chr5:103398600-103399000	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
30	chr5:103398600-103399000	Enhancers	iPS-20b Cell Line	embryonic stem cell
31	chr5:103398600-103399000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
32	chr5:103398600-103399000	Enhancers	Rectal Mucosa Donor 31	rectum
33	chr5:103398600-103399000	Enhancers	Osteobl	bone
34	chr5:103398600-103399200	Enhancers	HUES64 Cell Line	embryonic stem cell
35	chr5:103399000-103400800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
36	chr5:103400000-103400400	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
37	chr5:103400400-103400600	Weak transcription	HUES6 Cell Line	embryonic stem cell
38	chr5:103400600-103402800	Strong transcription	HUES6 Cell Line	embryonic stem cell
39	chr5:103400800-103401000	Strong transcription	ES-I3 Cell Line	embryonic stem cell
40	chr5:103401000-103401200	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
41	chr5:103401200-103407000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
42	chr5:103402000-103404200	Strong transcription	HUES48 Cell Line	embryonic stem cell
43	chr5:103402800-103403800	Weak transcription	HUES6 Cell Line	embryonic stem cell
44	chr5:103403800-103405400	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
45	chr5:103404000-103404400	Active TSS	iPS-15b Cell Line	embryonic stem cell
46	chr5:103404200-103406000	Weak transcription	HUES48 Cell Line	embryonic stem cell
47	chr5:103407200-103407400	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
48	chr5:103415600-103416800	Active TSS	ES-I3 Cell Line	embryonic stem cell
49	chr5:103416000-103417600	Active TSS	K562	blood
50	chr5:103416200-103416800	Active TSS	A549	lung

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