Variant report

Variant	nsv1024374
Chromosome Location	chr5:117882620-117909965
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:117884442-117884668	HepG2	liver:	n/a	n/a
2	CEBPB	chr5:117884396-117884796	MCF-7	breast:	n/a	chr5:117884623-117884634 chr5:117884574-117884585
3	CEBPB	chr5:117898314-117898635	A549	lung:	n/a	chr5:117898390-117898403 chr5:117898387-117898404 chr5:117898482-117898495 chr5:117898484-117898493 chr5:117898484-117898493 chr5:117898484-117898493 chr5:117898484-117898493
4	CEBPB	chr5:117898330-117898641	IMR90	lung:	n/a	chr5:117898390-117898403 chr5:117898387-117898404 chr5:117898482-117898495 chr5:117898484-117898493 chr5:117898484-117898493 chr5:117898484-117898493 chr5:117898484-117898493
5	CEBPB	chr5:117898360-117898614	MCF-7	breast:	n/a	chr5:117898390-117898403 chr5:117898387-117898404 chr5:117898482-117898495 chr5:117898484-117898493 chr5:117898484-117898493 chr5:117898484-117898493 chr5:117898484-117898493
6	CEBPB	chr5:117884508-117884707	HepG2	liver:	n/a	chr5:117884623-117884634 chr5:117884574-117884585
7	CEBPB	chr5:117884538-117884752	A549	lung:	n/a	chr5:117884623-117884634 chr5:117884574-117884585
8	CEBPB	chr5:117884436-117884805	Hela-S3	cervix:	n/a	chr5:117884623-117884634 chr5:117884574-117884585
9	CEBPB	chr5:117884404-117884771	HCT-116	colon:	n/a	chr5:117884623-117884634 chr5:117884574-117884585
10	CEBPB	chr5:117884333-117884820	HCT-116	colon:	n/a	chr5:117884623-117884634 chr5:117884574-117884585
11	CEBPB	chr5:117884403-117884809	HepG2	liver:	n/a	chr5:117884623-117884634 chr5:117884574-117884585
12	CEBPB	chr5:117893153-117893464	HepG2	liver:	n/a	chr5:117893294-117893305
13	CEBPB	chr5:117898345-117898611	Hela-S3	cervix:	n/a	chr5:117898390-117898403 chr5:117898387-117898404 chr5:117898482-117898495 chr5:117898484-117898493 chr5:117898484-117898493 chr5:117898484-117898493 chr5:117898484-117898493
14	CEBPB	chr5:117884451-117884780	IMR90	lung:	n/a	chr5:117884623-117884634 chr5:117884574-117884585
15	CEBPB	chr5:117898339-117898607	H1-hESC	embryonic stem cell:	n/a	chr5:117898390-117898403 chr5:117898387-117898404 chr5:117898482-117898495 chr5:117898484-117898493 chr5:117898484-117898493 chr5:117898484-117898493 chr5:117898484-117898493
16	CEBPB	chr5:117898306-117898626	HepG2	liver:	n/a	chr5:117898390-117898403 chr5:117898387-117898404 chr5:117898482-117898495 chr5:117898484-117898493 chr5:117898484-117898493 chr5:117898484-117898493 chr5:117898484-117898493
17	CEBPB	chr5:117884446-117884760	HepG2	liver:	n/a	chr5:117884623-117884634 chr5:117884574-117884585
18	CEBPB	chr5:117884363-117884907	MCF-7	breast:	n/a	chr5:117884623-117884634 chr5:117884574-117884585
19	CEBPB	chr5:117889409-117889983	IMR90	lung:	n/a	chr5:117889970-117889981 chr5:117889559-117889576 chr5:117889970-117889983 chr5:117889970-117889981
20	CEBPB	chr5:117898380-117898661	K562	blood:	n/a	chr5:117898390-117898403 chr5:117898387-117898404 chr5:117898482-117898495 chr5:117898484-117898493 chr5:117898484-117898493 chr5:117898484-117898493 chr5:117898484-117898493
21	CEBPD	chr5:117884545-117884701	HepG2	liver:	n/a	chr5:117884575-117884586
22	CTCF	chr5:117884566-117884680	MCF-7	breast:	n/a	chr5:117884609-117884627
23	CTCF	chr5:117884582-117884637	MCF-7	breast:	n/a	chr5:117884609-117884627
24	CTCF	chr5:117896000-117896150	AG09309	skin:	n/a	n/a
25	E2F4	chr5:117893214-117893313	MCF10A-Er-Src	breast:	n/a	n/a
26	E2F4	chr5:117889596-117889877	MCF10A-Er-Src	breast:	n/a	n/a
27	E2F4	chr5:117888245-117888395	MCF10A-Er-Src	breast:	n/a	n/a
28	E2F4	chr5:117884463-117884745	MCF10A-Er-Src	breast:	n/a	n/a
29	EBF1	chr5:117889422-117889705	GM12878	blood:	n/a	n/a
30	EBF1	chr5:117892621-117893203	GM12878	blood:	n/a	chr5:117893019-117893030 chr5:117893021-117893031
31	EP300	chr5:117889187-117889413	SK-N-SH_RA	brain:	n/a	n/a
32	EP300	chr5:117889226-117889689	SK-N-SH_RA	brain:	n/a	chr5:117889534-117889543
33	EP300	chr5:117889143-117889900	SK-N-SH	brain:	n/a	chr5:117889162-117889172 chr5:117889534-117889543
34	FOS	chr5:117901735-117901935	MCF10A-Er-Src	breast:	n/a	chr5:117901824-117901833 chr5:117901818-117901830 chr5:117901824-117901834 chr5:117901824-117901834 chr5:117901824-117901834 chr5:117901824-117901834
35	FOS	chr5:117894610-117894913	MCF10A-Er-Src	breast:	n/a	chr5:117894752-117894760 chr5:117894751-117894761 chr5:117894753-117894760 chr5:117894751-117894761 chr5:117894751-117894761 chr5:117894752-117894760 chr5:117894751-117894761
36	FOS	chr5:117884432-117884864	MCF10A-Er-Src	breast:	n/a	chr5:117884640-117884650 chr5:117884640-117884650
37	FOS	chr5:117901729-117901917	MCF10A-Er-Src	breast:	n/a	chr5:117901824-117901833 chr5:117901818-117901830 chr5:117901824-117901834 chr5:117901824-117901834 chr5:117901824-117901834 chr5:117901824-117901834
38	FOS	chr5:117889279-117889753	MCF10A-Er-Src	breast:	n/a	chr5:117889533-117889542 chr5:117889532-117889544 chr5:117889547-117889556 chr5:117889535-117889546
39	FOS	chr5:117894610-117894907	MCF10A-Er-Src	breast:	n/a	chr5:117894752-117894760 chr5:117894751-117894761 chr5:117894753-117894760 chr5:117894751-117894761 chr5:117894751-117894761 chr5:117894752-117894760 chr5:117894751-117894761
40	FOS	chr5:117884361-117885040	MCF10A-Er-Src	breast:	n/a	chr5:117884640-117884650 chr5:117884640-117884650
41	FOS	chr5:117894598-117894875	MCF10A-Er-Src	breast:	n/a	chr5:117894752-117894760 chr5:117894751-117894761 chr5:117894753-117894760 chr5:117894751-117894761 chr5:117894751-117894761 chr5:117894752-117894760 chr5:117894751-117894761
42	FOS	chr5:117901721-117901961	MCF10A-Er-Src	breast:	n/a	chr5:117901824-117901833 chr5:117901818-117901830 chr5:117901824-117901834 chr5:117901824-117901834 chr5:117901824-117901834 chr5:117901824-117901834
43	FOS	chr5:117884452-117884881	MCF10A-Er-Src	breast:	n/a	chr5:117884640-117884650 chr5:117884640-117884650
44	FOS	chr5:117901691-117901907	MCF10A-Er-Src	breast:	n/a	chr5:117901824-117901833 chr5:117901818-117901830 chr5:117901824-117901834 chr5:117901824-117901834 chr5:117901824-117901834 chr5:117901824-117901834
45	FOS	chr5:117889278-117889836	MCF10A-Er-Src	breast:	n/a	chr5:117889533-117889542 chr5:117889532-117889544 chr5:117889547-117889556 chr5:117889535-117889546
46	FOS	chr5:117884394-117884922	MCF10A-Er-Src	breast:	n/a	chr5:117884640-117884650 chr5:117884640-117884650
47	FOS	chr5:117889370-117889856	MCF10A-Er-Src	breast:	n/a	chr5:117889533-117889542 chr5:117889532-117889544 chr5:117889547-117889556 chr5:117889535-117889546
48	FOS	chr5:117886870-117887025	MCF10A-Er-Src	breast:	n/a	chr5:117886966-117886974 chr5:117886967-117886974
49	FOS	chr5:117889372-117889796	MCF10A-Er-Src	breast:	n/a	chr5:117889533-117889542 chr5:117889532-117889544 chr5:117889547-117889556 chr5:117889535-117889546
50	FOSL2	chr5:117889266-117889820	SK-N-SH	brain:	n/a	chr5:117889533-117889542 chr5:117889532-117889544 chr5:117889547-117889556 chr5:117889535-117889546

No.	Distal block	Cell Line	Cell type
1	chr5:117892457..117896152-chr5:117898946..117902524,3	MCF-7	breast:
2	chr5:117893334..117895634-chr5:117899247..117902608,3	K562	blood:
3	chr5:117892457..117896152-chr5:117898946..117902524,3	MCF-7	breast:
4	chr5:117893334..117895634-chr5:117899247..117902608,3	K562	blood:
5	chr5:117887915..117890272-chr5:117891445..117894908,3	MCF-7	breast:
6	chr5:117887915..117890272-chr5:117891445..117894908,3	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DTWD2-3	chr5:117890742-117890834	NONHSAT103403
2	lnc-DTWD2-3	chr5:117888048-117888244	XLOC_004965
3	lnc-DTWD2-3	chr5:117897616-117897751	XLOC_004965
4	lnc-DTWD2-3	chr5:117897616-117897812	NR_104610
5	lnc-DTWD2-10	chr5:117886321-117886440	l_3002_chr5:117837955-117925717_heart
6	lnc-DTWD2-3	chr5:117897616-117897812	XLOC_004965
7	lnc-DTWD2-3	chr5:117897616-117897812	NONHSAT103396
8	lnc-DTWD2-3	chr5:117897616-117897826	NONHSAT103403
9	lnc-DTWD2-3	chr5:117897616-117897818	XLOC_004965
10	lnc-DTWD2-10	chr5:117887243-117887411	l_3002_chr5:117837955-117925717_heart
11	lnc-DTWD2-3	chr5:117897616-117897818	XLOC_004965
12	lnc-DTWD2-10	chr5:117909342-117909743	l_3002_chr5:117837955-117925717_heart
13	lnc-DTWD2-3	chr5:117890742-117890834	XLOC_004965

Variant related genes	Relation type
ENSG00000249551	TF binding region
ENSG00000250891	TF binding region
HOXA5	miRNA target sites
SFRS2	miRNA target sites
KRAS	miRNA target sites
NR2C2AP	miRNA target sites

Extended variants
information (count: 1277 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:1277 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10054774	chr5:117882620-117882621	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs138163866	chr5:117882679-117882680	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs73788944	chr5:117882688-117882689	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs541832592	chr5:117882711-117882712	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs17144159	chr5:117882742-117882743	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs544235671	chr5:117882753-117882754	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs188765347	chr5:117882761-117882762	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs575696673	chr5:117882769-117882770	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs149536162	chr5:117882771-117882772	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs79630636	chr5:117882775-117882776	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs375772966	chr5:117882805-117882806	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs73788945	chr5:117882885-117882886	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs76787847	chr5:117882927-117882928	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs74499288	chr5:117882952-117882953	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs115066621	chr5:117882962-117882963	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs531208058	chr5:117882984-117882985	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs551330736	chr5:117883002-117883003	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs370382081	chr5:117883005-117883006	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs368058086	chr5:117883026-117883027	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs540061185	chr5:117883045-117883046	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs181718323	chr5:117883118-117883119	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs73247493	chr5:117883124-117883125	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs535238415	chr5:117883168-117883169	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs555342402	chr5:117883214-117883215	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs144095695	chr5:117883220-117883221	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs575162526	chr5:117883233-117883234	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs148249730	chr5:117883248-117883249	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs17435181	chr5:117883257-117883258	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs550640210	chr5:117883264-117883265	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs577368266	chr5:117883267-117883268	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs185435092	chr5:117883276-117883277	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs560128830	chr5:117883305-117883306	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs141241013	chr5:117883334-117883335	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs190243889	chr5:117883364-117883365	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs111365857	chr5:117883394-117883395	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs114986536	chr5:117883426-117883427	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs530944289	chr5:117883430-117883431	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs34450294	chr5:117883467-117883468	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs539195475	chr5:117883517-117883518	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs564774793	chr5:117883520-117883521	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs17144163	chr5:117883596-117883597	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs73788947	chr5:117883597-117883598	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs567004284	chr5:117883600-117883601	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs180789477	chr5:117883648-117883649	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs548818502	chr5:117883688-117883689	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs72795565	chr5:117883720-117883721	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs75676746	chr5:117883723-117883724	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs566419248	chr5:117883737-117883738	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs537450168	chr5:117883758-117883759	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs113551305	chr5:117883789-117883790	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:75)

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
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
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
Cancer	20164920	CNVD
Myelodysplastic syndrome	21251322	CNVD
Colorectal cancer	16272173	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Multiple myeloma	17550852	CNVD
Ovarian cancer	21720365	CNVD
Salivary gland tumor	18059337	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Renal cell carcinoma	19377443	CNVD
Prostate cancer	16461572	CNVD
Myelofibrosis	22110671	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Glaucoma	21310917	CNVD
Glioblastoma multiforme	22286061	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Breast cancer	21509527	CNVD
Autism	22543975	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:168 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:117880800-117884200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
2	chr5:117881000-117884200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
3	chr5:117883600-117887200	Enhancers	HMEC	breast
4	chr5:117883600-117887400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
5	chr5:117883600-117890800	Enhancers	NHDF-Ad	bronchial
6	chr5:117883800-117885200	Enhancers	Brain Germinal Matrix	brain
7	chr5:117883800-117891400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr5:117884200-117885200	Enhancers	Osteobl	bone
9	chr5:117884200-117885400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
10	chr5:117884200-117885400	Enhancers	Muscle Satellite Cultured Cells	--
11	chr5:117884200-117885600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
12	chr5:117884200-117885800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
13	chr5:117884200-117886000	Enhancers	NHLF	lung
14	chr5:117884200-117887200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr5:117884400-117885400	Enhancers	NH-A	brain
16	chr5:117884600-117885000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
17	chr5:117884800-117885200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
18	chr5:117885000-117885200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
19	chr5:117885000-117885800	Enhancers	Breast Myoepithelial Primary Cells	Breast
20	chr5:117885000-117892600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
21	chr5:117885200-117886000	Weak transcription	Brain Germinal Matrix	brain
22	chr5:117885200-117889200	Weak transcription	Osteobl	bone
23	chr5:117885200-117890800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
24	chr5:117885200-117894200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
25	chr5:117885400-117886800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
26	chr5:117885400-117889200	Weak transcription	Muscle Satellite Cultured Cells	--
27	chr5:117885400-117889600	Weak transcription	NH-A	brain
28	chr5:117885600-117887000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
29	chr5:117885800-117886200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
30	chr5:117885800-117892600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
31	chr5:117886000-117886200	Enhancers	Brain Germinal Matrix	brain
32	chr5:117886000-117889200	Weak transcription	NHLF	lung
33	chr5:117886200-117886600	Weak transcription	Brain Germinal Matrix	brain
34	chr5:117886200-117890800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
35	chr5:117886600-117887000	Enhancers	Brain Germinal Matrix	brain
36	chr5:117886800-117887400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
37	chr5:117887000-117887600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
38	chr5:117887200-117889200	Weak transcription	HMEC	breast
39	chr5:117887200-117889400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
40	chr5:117887400-117887800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
41	chr5:117887400-117889000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
42	chr5:117887600-117888000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
43	chr5:117887800-117889400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
44	chr5:117888000-117888200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
45	chr5:117888200-117889200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
46	chr5:117888400-117888600	Enhancers	Fetal Heart	heart
47	chr5:117888600-117892000	Weak transcription	Fetal Heart	heart
48	chr5:117889000-117890600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
49	chr5:117889200-117889600	Enhancers	ES-I3 Cell Line	embryonic stem cell
50	chr5:117889200-117889600	Enhancers	Adipose Nuclei	Adipose

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