Variant report

Variant	nsv1019939
Chromosome Location	chr5:103380722-103770101
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1728)
CpG islands
(count:0)
Chromatin interactive
region (count:102)
LncRNA
region (count:13)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1728 , 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	chr5:103424586-103425489	K562	blood:	n/a	n/a
2	ARID3A	chr5:103533944-103534020	HepG2	liver:	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	chr5:103427458-103427492	K562	blood:	n/a	n/a
6	ATF1	chr5:103582934-103583199	K562	blood:	n/a	n/a
7	ATF1	chr5:103525691-103525882	K562	blood:	n/a	n/a
8	ATF3	chr5:103525596-103526013	K562	blood:	n/a	chr5:103525833-103525847
9	ATF3	chr5:103425143-103425446	K562	blood:	n/a	n/a
10	BACH1	chr5:103425247-103425428	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr5:103424849-103425597	K562	blood:	n/a	n/a
12	BACH1	chr5:103420138-103420206	K562	blood:	n/a	n/a
13	BATF	chr5:103400582-103400825	GM12878	blood:	n/a	n/a
14	BATF	chr5:103425050-103425493	GM12878	blood:	n/a	chr5:103425282-103425293
15	BATF	chr5:103425096-103425463	GM12878	blood:	n/a	chr5:103425282-103425293
16	BCL11A	chr5:103425087-103425461	GM12878	blood:	n/a	chr5:103425281-103425290 chr5:103425282-103425291
17	BCL11A	chr5:103425108-103425491	GM12878	blood:	n/a	chr5:103425281-103425290 chr5:103425282-103425291
18	BCL3	chr5:103524584-103524828	GM12878	blood:	n/a	n/a
19	BHLHE40	chr5:103525586-103525928	K562	blood:	n/a	n/a
20	BHLHE40	chr5:103424858-103425183	K562	blood:	n/a	n/a
21	BHLHE40	chr5:103691018-103691342	HepG2	liver:	n/a	n/a
22	BHLHE40	chr5:103533950-103534025	HepG2	liver:	n/a	n/a
23	BHLHE40	chr5:103521859-103522065	K562	blood:	n/a	n/a
24	BRCA1	chr5:103508218-103508346	Hela-S3	cervix:	n/a	n/a
25	BRCA1	chr5:103681266-103681273	Hela-S3	cervix:	n/a	n/a
26	BRCA1	chr5:103514840-103515343	Hela-S3	cervix:	n/a	n/a
27	CBX3	chr5:103524709-103525168	K562	blood:	n/a	n/a
28	CBX3	chr5:103424834-103425657	HCT-116	colon:	n/a	n/a
29	CBX3	chr5:103440319-103440817	K562	blood:	n/a	n/a
30	CBX3	chr5:103521811-103522125	K562	blood:	n/a	n/a
31	CBX3	chr5:103525245-103525937	K562	blood:	n/a	n/a
32	CBX3	chr5:103521731-103522132	HCT-116	colon:	n/a	n/a
33	CBX3	chr5:103525630-103525950	K562	blood:	n/a	n/a
34	CBX3	chr5:103424562-103425521	K562	blood:	n/a	n/a
35	CBX3	chr5:103521726-103522181	K562	blood:	n/a	n/a
36	CBX3	chr5:103469878-103470276	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	chr5:103742238-103742359	H1-hESC	embryonic stem cell:	n/a	chr5:103742300-103742311
40	CEBPB	chr5:103680560-103680895	HepG2	liver:	n/a	chr5:103680714-103680725
41	CEBPB	chr5:103426963-103427303	IMR90	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
42	CEBPB	chr5:103521802-103522162	K562	blood:	n/a	chr5:103521977-103521988
43	CEBPB	chr5:103525665-103526003	Hela-S3	cervix:	n/a	n/a
44	CEBPB	chr5:103521808-103522127	K562	blood:	n/a	chr5:103521977-103521988
45	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
46	CEBPB	chr5:103427128-103427147	H1-hESC	embryonic stem cell:	n/a	chr5:103427132-103427145 chr5:103427134-103427143 chr5:103427134-103427143 chr5:103427132-103427145 chr5:103427132-103427145 chr5:103427132-103427143 chr5:103427133-103427144 chr5:103427134-103427143 chr5:103427132-103427143 chr5:103427134-103427143
47	CEBPB	chr5:103742141-103742471	HepG2	liver:	n/a	chr5:103742300-103742311
48	CEBPB	chr5:103406292-103406611	HepG2	liver:	n/a	n/a
49	CEBPB	chr5:103540971-103541049	K562	blood:	n/a	chr5:103541018-103541029 chr5:103541017-103541028
50	CEBPB	chr5:103521800-103522121	H1-hESC	embryonic stem cell:	n/a	chr5:103521977-103521988

No data

(count:102 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr5:103469361..103471032-chr5:103473793..103476182,2	K562	blood:
2	chr5:103414629..103417722-chr5:103419240..103423591,5	K562	blood:
3	chr5:103419555..103422324-chr5:103423618..103426898,4	K562	blood:
4	chr5:103467212..103468815-chr5:103480734..103482743,2	K562	blood:
5	chr5:103630146..103633049-chr5:103637946..103640879,3	K562	blood:
6	chr5:103614351..103617259-chr5:103627051..103629322,2	K562	blood:
7	chr5:103488217..103490726-chr5:103523272..103524966,2	K562	blood:
8	chr5:103440945..103442591-chr5:103463038..103465422,2	K562	blood:
9	chr16:4895983..4898171-chr5:103612146..103614008,2	MCF-7	breast:
10	chr5:103761403..103764401-chr5:103998452..104000157,2	MCF-7	breast:
11	chr5:103457491..103460470-chr5:103461243..103465378,4	K562	blood:
12	chr5:103574324..103576071-chr5:103577725..103579233,2	K562	blood:
13	chr5:103614351..103617259-chr5:103627051..103629322,2	K562	blood:
14	chr5:103547602..103549522-chr5:103555358..103558237,2	K562	blood:
15	chr5:103580298..103582448-chr5:103583760..103585414,2	MCF-7	breast:
16	chr5:102593172..102596932-chr5:103420035..103422975,3	K562	blood:
17	chr5:103143979..103144697-chr5:103514544..103515454,4	K562	blood:
18	chr5:103424304..103427061-chr5:103434256..103435929,2	K562	blood:
19	chr5:103431462..103433805-chr5:103436805..103438651,2	K562	blood:
20	chr5:103720063..103721767-chr5:103728887..103730529,2	MCF-7	breast:
21	chr5:103438292..103439842-chr5:103445545..103447443,2	MCF-7	breast:
22	chr5:103755525..103757594-chr5:103760680..103762734,2	K562	blood:
23	chr5:103720063..103721767-chr5:103728887..103730529,2	MCF-7	breast:
24	chr5:103568513..103570154-chr5:103579261..103581624,2	K562	blood:
25	chr15:100541763..100542576-chr5:103512576..103513415,2	MCF-7	breast:
26	chr5:103598709..103601053-chr5:103607200..103608906,2	K562	blood:
27	chr5:103575723..103577605-chr5:103642604..103644571,2	K562	blood:
28	chr5:103581733..103583397-chr5:103587148..103588917,2	MCF-7	breast:
29	chr5:103445190..103447987-chr5:103454013..103455945,2	K562	blood:
30	chr5:103504487..103508742-chr5:103509430..103512265,3	K562	blood:
31	chr5:103541472..103544045-chr5:103667629..103669884,2	K562	blood:
32	chr5:103406028..103408953-chr5:103419618..103421464,2	K562	blood:
33	chr5:103614287..103617162-chr5:103624383..103626582,2	K562	blood:
34	chr5:103747998..103750504-chr5:103755568..103757533,2	MCF-7	breast:
35	chr5:103614287..103617162-chr5:103624383..103626582,2	K562	blood:
36	chr5:102976878..102978536-chr5:103450055..103452229,2	K562	blood:
37	chr5:103581733..103583397-chr5:103587148..103588917,2	MCF-7	breast:
38	chr5:44578647..44579149-chr5:103415633..103416333,2	Hela-S3	cervix:
39	chr5:103677480..103679978-chr5:103685994..103688346,2	K562	blood:
40	chr5:103530400..103532599-chr5:103544330..103547134,2	K562	blood:
41	chr5:103493121..103495084-chr5:103495998..103498553,2	K562	blood:
42	chr5:103472133..103474624-chr5:103476667..103479218,2	K562	blood:
43	chr5:103662029..103663844-chr5:103689569..103691158,2	MCF-7	breast:
44	chr5:103427770..103429780-chr5:103432412..103434956,2	K562	blood:
45	chr5:103424892..103429270-chr5:103431386..103433912,4	K562	blood:
46	chr5:103431462..103433805-chr5:103436805..103438651,2	K562	blood:
47	chr5:103419555..103422324-chr5:103423618..103426898,4	K562	blood:
48	chr5:103619639..103621468-chr5:103623035..103624984,2	K562	blood:
49	chr5:103574324..103576071-chr5:103577725..103579233,2	K562	blood:
50	chr5:103440945..103442591-chr5:103463038..103465422,2	K562	blood:

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

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

No data

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

Extended variants
information (count: 7017 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:7017 , 50 per page) page: 1 2 3 4 5 6 7 ... 141

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs114191690	chr5:103380728-103380729	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs572495658	chr5:103380730-103380731	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs114584170	chr5:103380769-103380770	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs533126585	chr5:103380784-103380785	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs185447610	chr5:103380798-103380799	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs191086814	chr5:103380813-103380814	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs182454094	chr5:103380904-103380905	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs541885488	chr5:103380972-103380973	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs187388537	chr5:103380973-103380974	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs34736069	chr5:103380985-103380986	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs138967617	chr5:103381009-103381010	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs373594008	chr5:103381010-103381011	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs72309360	chr5:103381019-103381020	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs397882772	chr5:103381030-103381031	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs561231378	chr5:103381031-103381032	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs562359937	chr5:103381070-103381071	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs75391520	chr5:103381129-103381130	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs141965071	chr5:103381132-103381133	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs541198093	chr5:103381176-103381177	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs564642933	chr5:103381181-103381182	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs554525149	chr5:103381248-103381249	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs533378315	chr5:103381253-103381254	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs146120614	chr5:103381257-103381258	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs568890141	chr5:103381264-103381265	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs537847946	chr5:103381275-103381276	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs547820381	chr5:103381342-103381343	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs567724995	chr5:103381354-103381355	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs191816916	chr5:103381430-103381431	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs139043039	chr5:103381570-103381571	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs918152	chr5:103381572-103381573	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs183013482	chr5:103381594-103381595	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs539289288	chr5:103381599-103381600	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs556598901	chr5:103381611-103381612	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs550082850	chr5:103381613-103381614	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs187349498	chr5:103381628-103381629	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs562017015	chr5:103381642-103381643	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs572496177	chr5:103381678-103381679	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs74624431	chr5:103381686-103381687	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs541713108	chr5:103381774-103381775	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs565249026	chr5:103381834-103381835	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs533550903	chr5:103381857-103381858	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs116025284	chr5:103381886-103381887	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs562592334	chr5:103381890-103381891	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs114788301	chr5:103381891-103381892	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs547881604	chr5:103381913-103381914	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs1990745	chr5:103381922-103381923	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs142251703	chr5:103381969-103381970	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs547272886	chr5:103381978-103381979	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs569827884	chr5:103381981-103381982	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs201889780	chr5:103382047-103382048	Enhancers 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:414 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:103378600-103381000	Weak transcription	Ovary	ovary
2	chr5:103381000-103381200	Enhancers	Ovary	ovary
3	chr5:103381000-103381400	Enhancers	HUES64 Cell Line	embryonic stem cell
4	chr5:103381000-103382000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr5:103381200-103381800	Weak transcription	Ovary	ovary
6	chr5:103381600-103382000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr5:103381600-103382200	Enhancers	Fetal Lung	lung
8	chr5:103381800-103382000	Enhancers	Ovary	ovary
9	chr5:103382000-103385600	Weak transcription	Ovary	ovary
10	chr5:103382200-103383800	Weak transcription	Fetal Lung	lung
11	chr5:103383800-103384000	Enhancers	Fetal Lung	lung
12	chr5:103383800-103384000	Enhancers	Osteobl	bone
13	chr5:103383800-103384600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
14	chr5:103384000-103384400	Weak transcription	Fetal Lung	lung
15	chr5:103384000-103384600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
16	chr5:103384400-103384600	Enhancers	Fetal Lung	lung
17	chr5:103384600-103385800	Weak transcription	Fetal Lung	lung
18	chr5:103385600-103386200	Enhancers	Ovary	ovary
19	chr5:103385800-103387000	Enhancers	Fetal Lung	lung
20	chr5:103386200-103386800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
21	chr5:103386200-103386800	Weak transcription	Ovary	ovary
22	chr5:103386800-103387000	Enhancers	Ovary	ovary
23	chr5:103386800-103388800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
24	chr5:103388400-103388600	Enhancers	Brain Cingulate Gyrus	brain
25	chr5:103388800-103389000	Enhancers	Fetal Lung	lung
26	chr5:103388800-103389200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
27	chr5:103388800-103389200	Enhancers	Colon Smooth Muscle	Colon
28	chr5:103395600-103397000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr5:103396800-103397200	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
30	chr5:103397200-103402000	Weak transcription	HUES48 Cell Line	embryonic stem cell
31	chr5:103397800-103398400	Enhancers	iPS-15b Cell Line	embryonic stem cell
32	chr5:103398400-103398600	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
33	chr5:103398400-103398800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
34	chr5:103398400-103398800	Active TSS	Rectal Mucosa Donor 29	rectum
35	chr5:103398400-103404000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
36	chr5:103398600-103398800	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
37	chr5:103398600-103399000	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
38	chr5:103398600-103399000	Enhancers	iPS-20b Cell Line	embryonic stem cell
39	chr5:103398600-103399000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
40	chr5:103398600-103399000	Enhancers	Rectal Mucosa Donor 31	rectum
41	chr5:103398600-103399000	Enhancers	Osteobl	bone
42	chr5:103398600-103399200	Enhancers	HUES64 Cell Line	embryonic stem cell
43	chr5:103399000-103400800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
44	chr5:103400000-103400400	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
45	chr5:103400400-103400600	Weak transcription	HUES6 Cell Line	embryonic stem cell
46	chr5:103400600-103402800	Strong transcription	HUES6 Cell Line	embryonic stem cell
47	chr5:103400800-103401000	Strong transcription	ES-I3 Cell Line	embryonic stem cell
48	chr5:103401000-103401200	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
49	chr5:103401200-103407000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
50	chr5:103402000-103404200	Strong transcription	HUES48 Cell Line	embryonic stem cell

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