Variant report

Variant	nsv599205
Chromosome Location	chr5:103478518-103614650
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:685)
CpG islands
(count:0)
Chromatin interactive
region (count:38)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:685 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

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	ATF1	chr5:103525691-103525882	K562	blood:	n/a	n/a
3	ATF1	chr5:103582934-103583199	K562	blood:	n/a	n/a
4	ATF3	chr5:103525596-103526013	K562	blood:	n/a	chr5:103525833-103525847
5	BCL3	chr5:103524584-103524828	GM12878	blood:	n/a	n/a
6	BHLHE40	chr5:103521859-103522065	K562	blood:	n/a	n/a
7	BHLHE40	chr5:103525586-103525928	K562	blood:	n/a	n/a
8	BHLHE40	chr5:103533950-103534025	HepG2	liver:	n/a	n/a
9	BRCA1	chr5:103514840-103515343	Hela-S3	cervix:	n/a	n/a
10	BRCA1	chr5:103508218-103508346	Hela-S3	cervix:	n/a	n/a
11	CBX3	chr5:103524709-103525168	K562	blood:	n/a	n/a
12	CBX3	chr5:103521726-103522181	K562	blood:	n/a	n/a
13	CBX3	chr5:103521731-103522132	HCT-116	colon:	n/a	n/a
14	CBX3	chr5:103521811-103522125	K562	blood:	n/a	n/a
15	CBX3	chr5:103525245-103525937	K562	blood:	n/a	n/a
16	CBX3	chr5:103525630-103525950	K562	blood:	n/a	n/a
17	CCNT2	chr5:103526459-103526708	K562	blood:	n/a	n/a
18	CEBPB	chr5:103521884-103522031	K562	blood:	n/a	chr5:103521977-103521988
19	CEBPB	chr5:103525665-103526003	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr5:103515939-103516171	HepG2	liver:	n/a	chr5:103516021-103516032
21	CEBPB	chr5:103535465-103535937	Hela-S3	cervix:	n/a	n/a
22	CEBPB	chr5:103540971-103541049	K562	blood:	n/a	chr5:103541018-103541029 chr5:103541017-103541028
23	CEBPB	chr5:103521819-103522154	Hela-S3	cervix:	n/a	chr5:103521977-103521988
24	CEBPB	chr5:103533994-103534173	HepG2	liver:	n/a	n/a
25	CEBPB	chr5:103612671-103612913	HepG2	liver:	n/a	chr5:103612792-103612801 chr5:103612790-103612801 chr5:103612792-103612803 chr5:103612792-103612801 chr5:103612792-103612803 chr5:103612790-103612803 chr5:103612792-103612801 chr5:103612792-103612801
26	CEBPB	chr5:103593790-103593850	HepG2	liver:	n/a	chr5:103593815-103593826
27	CEBPB	chr5:103507748-103508390	Hela-S3	cervix:	n/a	chr5:103508169-103508180 chr5:103508169-103508182 chr5:103507982-103507995
28	CEBPB	chr5:103508091-103508291	HepG2	liver:	n/a	chr5:103508169-103508180 chr5:103508169-103508182
29	CEBPB	chr5:103521802-103522162	K562	blood:	n/a	chr5:103521977-103521988
30	CEBPB	chr5:103557837-103558073	A549	lung:	n/a	chr5:103557944-103557955
31	CEBPB	chr5:103540915-103541119	HepG2	liver:	n/a	chr5:103541018-103541029 chr5:103541017-103541028
32	CEBPB	chr5:103557803-103558074	HepG2	liver:	n/a	chr5:103557944-103557955
33	CEBPB	chr5:103521800-103522121	H1-hESC	embryonic stem cell:	n/a	chr5:103521977-103521988
34	CEBPB	chr5:103521855-103522159	HepG2	liver:	n/a	chr5:103521977-103521988
35	CEBPB	chr5:103521808-103522127	K562	blood:	n/a	chr5:103521977-103521988
36	CEBPB	chr5:103499677-103499895	HepG2	liver:	n/a	n/a
37	CEBPB	chr5:103524784-103525127	Hela-S3	cervix:	n/a	n/a
38	CEBPB	chr5:103514816-103515170	Hela-S3	cervix:	n/a	n/a
39	CEBPB	chr5:103612753-103612837	K562	blood:	n/a	chr5:103612792-103612801 chr5:103612790-103612801 chr5:103612792-103612803 chr5:103612792-103612801 chr5:103612792-103612803 chr5:103612790-103612803 chr5:103612792-103612801 chr5:103612792-103612801
40	CEBPB	chr5:103489580-103489920	Hela-S3	cervix:	n/a	n/a
41	CEBPB	chr5:103539579-103539670	K562	blood:	n/a	n/a
42	CREB1	chr5:103514801-103515037	A549	lung:	n/a	n/a
43	CTCF	chr5:103514840-103514990	HFF	foreskin:	n/a	n/a
44	CTCF	chr5:103514811-103515166	K562	blood:	n/a	n/a
45	CTCF	chr5:103514920-103515070	GM12864	blood:	n/a	n/a
46	CTCF	chr5:103499760-103499910	Caco-2	colon:	n/a	n/a
47	CTCF	chr5:103514920-103515070	HEEpiC	esophagus:	n/a	n/a
48	CTCF	chr5:103541500-103541650	HPF	lung:	n/a	n/a
49	CTCF	chr5:103514855-103515161	K562	blood:	n/a	n/a
50	CTCF	chr5:103514940-103515090	GM12864	blood:	n/a	n/a

No data

(count:38 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:103547602..103549522-chr5:103555358..103558237,2	K562	blood:
2	chr5:103568513..103570154-chr5:103579261..103581624,2	K562	blood:
3	chr5:103581733..103583397-chr5:103587148..103588917,2	MCF-7	breast:
4	chr5:103614287..103617162-chr5:103624383..103626582,2	K562	blood:
5	chr5:103575723..103577605-chr5:103642604..103644571,2	K562	blood:
6	chr5:103504487..103508742-chr5:103509430..103512265,3	K562	blood:
7	chr5:103580298..103582448-chr5:103583760..103585414,2	MCF-7	breast:
8	chr5:103568513..103570154-chr5:103579261..103581624,2	K562	blood:
9	chr5:103547602..103549522-chr5:103555358..103558237,2	K562	blood:
10	chr5:103598709..103601053-chr5:103607200..103608906,2	K562	blood:
11	chr5:103488217..103490726-chr5:103523272..103524966,2	K562	blood:
12	chr5:103467212..103468815-chr5:103480734..103482743,2	K562	blood:
13	chr15:100541763..100542576-chr5:103512576..103513415,2	MCF-7	breast:
14	chr5:103541472..103544045-chr5:103667629..103669884,2	K562	blood:
15	chr5:103519669..103522372-chr5:103523463..103525716,2	K562	blood:
16	chr5:103471677..103474624-chr5:103476498..103479218,3	K562	blood:
17	chr5:103500874..103502954-chr5:103505978..103507826,2	K562	blood:
18	chr5:103519669..103522372-chr5:103523463..103525716,2	K562	blood:
19	chr5:103579485..103581978-chr5:103587465..103589014,2	MCF-7	breast:
20	chr5:103530400..103532599-chr5:103544330..103547134,2	K562	blood:
21	chr5:103488217..103490726-chr5:103523272..103524966,2	K562	blood:
22	chr5:103493121..103495084-chr5:103495998..103498553,2	K562	blood:
23	chr5:103472133..103474624-chr5:103476667..103479218,2	K562	blood:
24	chr16:4895983..4898171-chr5:103612146..103614008,2	MCF-7	breast:
25	chr5:103598709..103601053-chr5:103607200..103608906,2	K562	blood:
26	chr5:103574324..103576071-chr5:103577725..103579233,2	K562	blood:
27	chr5:103581733..103583397-chr5:103587148..103588917,2	MCF-7	breast:
28	chr5:103574324..103576071-chr5:103577725..103579233,2	K562	blood:
29	chr5:103530400..103532599-chr5:103544330..103547134,2	K562	blood:
30	chr5:103500874..103502954-chr5:103505978..103507826,2	K562	blood:
31	chr5:103493121..103495084-chr5:103495998..103498553,2	K562	blood:
32	chr5:103143979..103144697-chr5:103514544..103515454,4	K562	blood:
33	chr5:103613010..103614607-chr5:103618160..103620311,2	MCF-7	breast:
34	chr18:25069473..25070359-chr5:103536312..103537041,2	MCF-7	breast:
35	chr5:103504487..103508742-chr5:103509430..103512265,3	K562	blood:
36	chr5:103579485..103581978-chr5:103587465..103589014,2	MCF-7	breast:
37	chr5:103614351..103617259-chr5:103627051..103629322,2	K562	blood:
38	chr5:103580298..103582448-chr5:103583760..103585414,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NUDT12-12	chr5:103596234-103596527	NONHSAT103075

No data

Variant related genes	Relation type
RN7SL255P	TF binding region
ENSG00000140632	chromatin interactions
ENSG00000118900	chromatin interactions

Extended variants
information (count: 2057 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:2057 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs555589437	chr5:103480258-103480259	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs572248608	chr5:103480303-103480304	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs549273826	chr5:103480350-103480351	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs34822639	chr5:103480351-103480352	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs541269916	chr5:103480402-103480403	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs564249869	chr5:103480416-103480417	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs17156182	chr5:103480433-103480434	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs145841622	chr5:103480441-103480442	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs563541584	chr5:103480455-103480456	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs529237228	chr5:103480466-103480467	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs11748709	chr5:103480474-103480475	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
12	rs560033348	chr5:103480480-103480481	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs529005204	chr5:103480501-103480502	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs528763701	chr5:103480519-103480520	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs551588776	chr5:103480561-103480562	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs35090102	chr5:103480611-103480612	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs140147528	chr5:103480616-103480617	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs35150559	chr5:103480617-103480618	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs397882304	chr5:103480618-103480619	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs4067550	chr5:103480620-103480621	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs539164913	chr5:103480629-103480630	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs17340741	chr5:103480650-103480651	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs569554386	chr5:103480657-103480658	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs535482263	chr5:103480702-103480703	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs555060012	chr5:103480785-103480786	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs191403047	chr5:103480800-103480801	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs117726280	chr5:103480821-103480822	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs369787154	chr5:103480857-103480858	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs182676085	chr5:103480877-103480878	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs115080169	chr5:103480970-103480971	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs139272340	chr5:103480980-103480981	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs186018620	chr5:103480992-103480993	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs543040716	chr5:103481001-103481002	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs3857362	chr5:103481012-103481013	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
35	rs528784577	chr5:103481014-103481015	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs545265031	chr5:103481019-103481020	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs73775539	chr5:103481032-103481033	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs530963877	chr5:103481044-103481045	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs113273603	chr5:103481065-103481066	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs544137156	chr5:103481066-103481067	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs528903044	chr5:103481069-103481070	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs397828762	chr5:103481086-103481087	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs550759379	chr5:103481119-103481120	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs569773704	chr5:103481137-103481138	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs72775042	chr5:103481174-103481175	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs371899278	chr5:103481258-103481259	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs115760409	chr5:103481280-103481281	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs565505057	chr5:103481354-103481355	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs113299738	chr5:103481466-103481467	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs78978764	chr5:103481475-103481476	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:82)

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

Chromatin state (count:148 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:103480200-103480800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr5:103480400-103483400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr5:103480800-103481000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr5:103481000-103482400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr5:103482000-103483000	Enhancers	Colon Smooth Muscle	Colon
6	chr5:103482200-103483000	Enhancers	Rectal Smooth Muscle	rectum
7	chr5:103482200-103483400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
8	chr5:103482200-103483400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr5:103482400-103483000	Enhancers	Muscle Satellite Cultured Cells	--
10	chr5:103482400-103483400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr5:103482400-103483400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
12	chr5:103482400-103483400	Enhancers	Fetal Kidney	kidney
13	chr5:103482400-103483600	Enhancers	Fetal Lung	lung
14	chr5:103482800-103483400	Enhancers	Fetal Stomach	stomach
15	chr5:103496200-103496800	Enhancers	Fetal Kidney	kidney
16	chr5:103496600-103497000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
17	chr5:103506400-103507000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
18	chr5:103507000-103507400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr5:103507400-103508400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
20	chr5:103507600-103509000	Enhancers	Hela-S3	cervix
21	chr5:103509000-103510200	Weak transcription	Hela-S3	cervix
22	chr5:103513600-103514600	Weak transcription	Hela-S3	cervix
23	chr5:103514600-103515200	Enhancers	Hela-S3	cervix
24	chr5:103514600-103515600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr5:103514800-103515000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
26	chr5:103514800-103516200	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
27	chr5:103515600-103516600	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
28	chr5:103520000-103520800	Enhancers	Muscle Satellite Cultured Cells	--
29	chr5:103521200-103525000	Enhancers	Skeletal Muscle Male	skeletal muscle
30	chr5:103521400-103521600	Active TSS	Liver	Liver
31	chr5:103521600-103521800	Enhancers	Liver	Liver
32	chr5:103521800-103522000	ZNF genes & repeats	Liver	Liver
33	chr5:103521800-103522000	Enhancers	NHEK	skin
34	chr5:103522000-103522400	Weak transcription	Muscle Satellite Cultured Cells	--
35	chr5:103522000-103522400	Flanking Active TSS	NHEK	skin
36	chr5:103522000-103525000	Enhancers	Skeletal Muscle Female	skeletal muscle
37	chr5:103522200-103522800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
38	chr5:103522400-103524600	Weak transcription	NHEK	skin
39	chr5:103524000-103525400	Weak transcription	K562	blood
40	chr5:103524400-103524800	Enhancers	Placenta Amnion	Placenta Amnion
41	chr5:103524400-103524800	Enhancers	Psoas Muscle	Psoas
42	chr5:103524400-103525200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
43	chr5:103524400-103526000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
44	chr5:103524400-103526200	Enhancers	NH-A	brain
45	chr5:103524400-103526200	Enhancers	Osteobl	bone
46	chr5:103524400-103526400	Enhancers	Muscle Satellite Cultured Cells	--
47	chr5:103524400-103526600	Enhancers	Hela-S3	cervix
48	chr5:103524600-103525800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
49	chr5:103524600-103526200	Enhancers	HMEC	breast
50	chr5:103524600-103526200	Enhancers	NHEK	skin

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