Variant report

Variant	nsv882627
Chromosome Location	chr5:104721409-104874282
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:482)
CpG islands
(count:183)
Chromatin interactive
region (count:27)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:482 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:104726542-104727019	K562	blood:	n/a	n/a
2	ARID3A	chr5:104728602-104728921	K562	blood:	n/a	n/a
3	ARID3A	chr5:104729126-104729280	K562	blood:	n/a	n/a
4	ATF1	chr5:104728486-104728895	K562	blood:	n/a	n/a
5	ATF1	chr5:104733331-104733371	K562	blood:	n/a	n/a
6	BACH1	chr5:104738330-104738373	K562	blood:	n/a	n/a
7	BACH1	chr5:104779909-104779930	K562	blood:	n/a	n/a
8	BHLHE40	chr5:104728493-104728748	K562	blood:	n/a	n/a
9	BRCA1	chr5:104868861-104868905	Hela-S3	cervix:	n/a	n/a
10	CBX3	chr5:104796463-104796676	K562	blood:	n/a	n/a
11	CBX3	chr5:104866626-104866912	K562	blood:	n/a	n/a
12	CBX3	chr5:104755037-104755389	K562	blood:	n/a	n/a
13	CBX3	chr5:104728451-104728993	K562	blood:	n/a	n/a
14	CBX3	chr5:104728363-104729015	K562	blood:	n/a	n/a
15	CBX3	chr5:104755081-104755354	K562	blood:	n/a	n/a
16	CBX3	chr5:104796414-104796740	K562	blood:	n/a	n/a
17	CBX3	chr5:104866542-104866887	K562	blood:	n/a	n/a
18	CCNT2	chr5:104727769-104728552	K562	blood:	n/a	n/a
19	CEBPB	chr5:104859757-104859805	K562	blood:	n/a	chr5:104859773-104859784
20	CEBPB	chr5:104780741-104780853	K562	blood:	n/a	n/a
21	CEBPB	chr5:104859617-104859857	A549	lung:	n/a	chr5:104859773-104859784
22	CEBPB	chr5:104845452-104845652	H1-hESC	embryonic stem cell:	n/a	n/a
23	CEBPB	chr5:104859631-104860027	HepG2	liver:	n/a	chr5:104859773-104859784
24	CEBPB	chr5:104788546-104788789	A549	lung:	n/a	chr5:104788606-104788619 chr5:104788606-104788617 chr5:104788603-104788620
25	CEBPB	chr5:104872393-104872674	HepG2	liver:	n/a	n/a
26	CEBPB	chr5:104847008-104847283	K562	blood:	n/a	chr5:104847143-104847156
27	CEBPB	chr5:104872469-104872684	K562	blood:	n/a	n/a
28	CEBPB	chr5:104788448-104788780	HepG2	liver:	n/a	chr5:104788606-104788619 chr5:104788606-104788617 chr5:104788603-104788620
29	CEBPB	chr5:104783657-104783915	HepG2	liver:	n/a	chr5:104783784-104783795
30	CHD2	chr5:104728384-104728863	K562	blood:	n/a	n/a
31	CHD2	chr5:104727637-104727834	K562	blood:	n/a	n/a
32	CHD2	chr5:104796530-104796598	H1-hESC	embryonic stem cell:	n/a	n/a
33	CTCF	chr5:104842660-104842810	NHEK	skin:	n/a	n/a
34	CTCF	chr5:104842540-104842690	GM12871	blood:	n/a	n/a
35	CTCF	chr5:104842420-104842710	A549	lung:	n/a	n/a
36	CTCF	chr5:104842520-104842670	HCPEpiC	choroid plexus:	n/a	n/a
37	CTCF	chr5:104842500-104842650	GM12878	blood:	n/a	n/a
38	CTCF	chr5:104842560-104842710	SAEC	small airway:	n/a	n/a
39	CTCF	chr5:104842536-104842644	Pancreas_OC	pancreas:	n/a	n/a
40	CTCF	chr5:104727909-104728007	K562	blood:	n/a	n/a
41	CTCF	chr5:104842512-104842680	A549	lung:	n/a	n/a
42	CTCF	chr5:104787945-104787991	Pancreas_OC	pancreas:	n/a	n/a
43	CTCF	chr5:104842440-104842710	GM12868	blood:	n/a	n/a
44	CTCF	chr5:104842440-104842590	HCT-116	colon:	n/a	n/a
45	CTCF	chr5:104842484-104842693	GM13977	blood:	n/a	n/a
46	CTCF	chr5:104842438-104842710	SK-N-SH_RA	brain:	n/a	n/a
47	CTCF	chr5:104842492-104842698	H1-hESC	embryonic stem cell:	n/a	n/a
48	CTCF	chr5:104842469-104842699	HUVEC	blood vessel:	n/a	n/a
49	CTCF	chr5:104842490-104842702	LNCaP	prostate:	n/a	n/a
50	CTCF	chr5:104842460-104842610	GM06990	blood:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:104854808-104854858	MCF-7	breast:	n/a
2	chr5:104854808-104854858	HAEpiC	amniotic membrane:	n/a
3	chr5:104854808-104854858	Caco-2	colon:	n/a
4	chr5:104854808-104854858	ovcar-3	ovarian:	n/a
5	chr5:104728220-104728270	NH-A	brain:	n/a
6	chr5:104854808-104854858	AG10803	skin:	n/a
7	chr5:104728427-104728477	HCF	heart:	n/a
8	chr5:104728220-104728270	GM12878	blood:	n/a
9	chr5:104728427-104728477	AG09309	skin:	n/a
10	chr5:104854808-104854858	AG09309	skin:	n/a
11	chr5:104854808-104854858	IMR90	lung:	fetal
12	chr5:104854808-104854858	GM06990	blood:	n/a
13	chr5:104728220-104728270	HRCEpiC	kidney:	n/a
14	chr5:104728427-104728477	HRE	kidney:	n/a
15	chr5:104728220-104728270	MCF10A-Er-Src	breast:	n/a
16	chr5:104728220-104728270	ProgFib	skin:	n/a
17	chr5:104728220-104728270	PrEC	prostate:	n/a
18	chr5:104728427-104728477	GM06990	blood:	n/a
19	chr5:104728220-104728270	BJ	skin:	n/a
20	chr5:104728220-104728270	PFSK-1	brain:	n/a
21	chr5:104854808-104854858	SK-N-SH	brain:	n/a
22	chr5:104728220-104728270	HAEpiC	amniotic membrane:	n/a
23	chr5:104854808-104854858	AG09319	gingival:	n/a
24	chr5:104728427-104728477	BJ	skin:	n/a
25	chr5:104854808-104854858	HCM	heart:	n/a
26	chr5:104728427-104728477	Jurkat	blood:	n/a
27	chr5:104728220-104728270	HRPEpiC	eye:	n/a
28	chr5:104728427-104728477	HAEpiC	amniotic membrane:	n/a
29	chr5:104728427-104728477	HRCEpiC	kidney:	n/a
30	chr5:104854808-104854858	GM19239	blood:	n/a
31	chr5:104728220-104728270	Hepatocyte	liver:	n/a
32	chr5:104728427-104728477	Caco-2	colon:	n/a
33	chr5:104728220-104728270	CMK	blood:	n/a
34	chr5:104728220-104728270	AoSMC	blood vessel:	n/a
35	chr5:104728427-104728477	SK-N-SH_RA	brain:	n/a
36	chr5:104728220-104728270	SK-N-SH	brain:	n/a
37	chr5:104854808-104854858	HUVEC	blood vessel:	n/a
38	chr5:104854808-104854858	SKMC	muscle:	n/a
39	chr5:104854808-104854858	HIPEpiC	eye:	n/a
40	chr5:104728220-104728270	AG09309	skin:	n/a
41	chr5:104728220-104728270	GM12891	blood:	n/a
42	chr5:104854808-104854858	BJ	skin:	n/a
43	chr5:104854808-104854858	H1-hESC	embryonic stem cell:	embryo
44	chr5:104728427-104728477	HEK293	kidney:	embryo
45	chr5:104854808-104854858	SK-N-SH_RA	brain:	n/a
46	chr5:104728427-104728477	ECC-1	luminal epithelium:	n/a
47	chr5:104728427-104728477	SK-N-SH	brain:	n/a
48	chr5:104728427-104728477	AG04449	skin:	fetal
49	chr5:104728220-104728270	T-47D	breast:	n/a
50	chr5:104854808-104854858	ProgFib	skin:	n/a

(count:27 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:104722652..104724763-chr5:104741861..104743629,2	K562	blood:
2	chr5:104723018..104724952-chr5:104737690..104739211,2	K562	blood:
3	chr5:104805339..104808156-chr5:104810446..104813222,2	MCF-7	breast:
4	chr5:104778136..104780320-chr5:104785388..104787017,2	K562	blood:
5	chr5:104733236..104736068-chr5:104886596..104888346,2	MCF-7	breast:
6	chr5:104740786..104743331-chr5:104745586..104748363,2	K562	blood:
7	chr5:104805339..104808156-chr5:104810446..104813222,2	MCF-7	breast:
8	chr5:104810915..104813579-chr5:104817384..104819206,2	MCF-7	breast:
9	chr4:114611671..114612572-chr5:104870661..104871343,2	MCF-7	breast:
10	chr5:104768629..104770858-chr5:104785097..104787270,2	K562	blood:
11	chr5:104740786..104743331-chr5:104745586..104748363,2	K562	blood:
12	chr5:104729079..104730844-chr5:104733038..104734650,2	K562	blood:
13	chr5:104723018..104724952-chr5:104737690..104739211,2	K562	blood:
14	chr5:104768629..104770858-chr5:104785097..104787270,2	K562	blood:
15	chr1:184434764..184435543-chr5:104792004..104792524,3	MCF-7	breast:
16	chr5:104726359..104728666-chr5:105131284..105132821,2	K562	blood:
17	chr5:104810915..104813579-chr5:104817384..104819206,2	MCF-7	breast:
18	chr5:104710520..104712024-chr5:104741469..104744150,2	K562	blood:
19	chr5:104727742..104729434-chr5:104763198..104765492,2	K562	blood:
20	chr5:104833860..104836077-chr5:104839152..104841039,2	K562	blood:
21	chr5:104722652..104724763-chr5:104741861..104743629,2	K562	blood:
22	chr5:104726534..104729492-chr5:107716153..107718681,2	K562	blood:
23	chr5:104778136..104780320-chr5:104785388..104787017,2	K562	blood:
24	chr5:104833860..104836077-chr5:104839152..104841039,2	K562	blood:
25	chr5:104727296..104728816-chr5:104790778..104793743,2	K562	blood:
26	chr18:42792470..42793145-chr5:104821622..104822504,2	MCF-7	breast:
27	chr5:104729079..104730844-chr5:104733038..104734650,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NUDT12-7	chr5:104728462-104728989	NONHSAT103097
2	lnc-NUDT12-6	chr5:104728462-104728671	ENSG00000251574

No data

Variant related genes	Relation type
ENSG00000251574	TF binding region
ENSG00000251574	CpG island
ENSG00000132874	chromatin interactions
ENSG00000251574	chromatin interactions
ENSG00000145743	chromatin interactions

Extended variants
information (count: 2207 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:2207 , 50 per page) page: 1 2 3 4 5 6 7 ... 45

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs556087121	chr5:104722002-104722003	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs193213303	chr5:104722034-104722035	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs11955463	chr5:104722062-104722063	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs72786079	chr5:104722072-104722073	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs572127539	chr5:104722079-104722080	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs375413183	chr5:104722110-104722111	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs541050877	chr5:104722131-104722132	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs185562880	chr5:104722136-104722137	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs564056253	chr5:104722161-104722162	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs75001211	chr5:104722164-104722165	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs544123140	chr5:104722172-104722173	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs187751653	chr5:104722239-104722240	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs375479981	chr5:104722252-104722253	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs72786080	chr5:104722261-104722262	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs559558535	chr5:104722275-104722276	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs548857574	chr5:104722285-104722286	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs562537092	chr5:104722292-104722293	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs528599609	chr5:104722372-104722373	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs112591478	chr5:104722426-104722427	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs191334928	chr5:104722427-104722428	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs57183746	chr5:104722481-104722482	Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs376863151	chr5:104722520-104722521	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs10069762	chr5:104722529-104722530	Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs549626329	chr5:104722531-104722532	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs569939996	chr5:104722560-104722561	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs183734911	chr5:104722593-104722594	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs550085800	chr5:104722595-104722596	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs555554407	chr5:104722615-104722616	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs572181207	chr5:104722639-104722640	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs534695005	chr5:104722676-104722677	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs188450339	chr5:104722682-104722683	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs371453644	chr5:104722706-104722707	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs538602351	chr5:104722730-104722731	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs142106961	chr5:104722734-104722735	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs181360640	chr5:104722747-104722748	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs184309549	chr5:104722748-104722749	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs10069907	chr5:104722755-104722756	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs190032288	chr5:104722799-104722800	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs559879730	chr5:104722815-104722816	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs565733091	chr5:104722855-104722856	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs528704682	chr5:104722905-104722906	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs147389513	chr5:104722906-104722907	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs367819238	chr5:104722909-104722910	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs182214138	chr5:104722910-104722911	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs57469653	chr5:104722915-104722916	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs76482840	chr5:104722916-104722917	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs550585651	chr5:104722922-104722923	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs117215731	chr5:104722923-104722924	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs139449940	chr5:104722933-104722934	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs58714934	chr5:104722938-104722939	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:84)

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
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
Myelofibrosis	22110671	CNVD
Obesity	20622171	CNVD
Lung cancer	16773561	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:75 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:104722000-104722200	Enhancers	HUES48 Cell Line	embryonic stem cell
2	chr5:104722200-104722600	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
3	chr5:104722200-104722800	Enhancers	HUES6 Cell Line	embryonic stem cell
4	chr5:104722200-104723200	Enhancers	HUES64 Cell Line	embryonic stem cell
5	chr5:104722400-104723400	Enhancers	iPS-15b Cell Line	embryonic stem cell
6	chr5:104722400-104723600	Enhancers	ES-I3 Cell Line	embryonic stem cell
7	chr5:104722600-104723000	Enhancers	HUES48 Cell Line	embryonic stem cell
8	chr5:104724800-104725800	Enhancers	K562	blood
9	chr5:104725800-104726400	Weak transcription	K562	blood
10	chr5:104726400-104729200	Active TSS	K562	blood
11	chr5:104727400-104727600	Enhancers	Placenta	Placenta
12	chr5:104727600-104727800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
13	chr5:104727600-104728000	Flanking Active TSS	Placenta	Placenta
14	chr5:104727600-104729000	Active TSS	HepG2	liver
15	chr5:104727800-104728000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr5:104727800-104728600	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
17	chr5:104728000-104728400	Active TSS	Placenta	Placenta
18	chr5:104728400-104728800	ZNF genes & repeats	Placenta	Placenta
19	chr5:104742400-104743400	Enhancers	HUES48 Cell Line	embryonic stem cell
20	chr5:104742400-104743600	Enhancers	HUES64 Cell Line	embryonic stem cell
21	chr5:104742400-104743600	Enhancers	iPS-15b Cell Line	embryonic stem cell
22	chr5:104742600-104743400	Enhancers	ES-I3 Cell Line	embryonic stem cell
23	chr5:104742800-104743200	Enhancers	HUES6 Cell Line	embryonic stem cell
24	chr5:104742800-104743400	Enhancers	iPS-18 Cell Line	embryonic stem cell
25	chr5:104748600-104749200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
26	chr5:104748800-104749200	Enhancers	HUES6 Cell Line	embryonic stem cell
27	chr5:104749200-104749600	Bivalent Enhancer	Placenta	Placenta
28	chr5:104749200-104749800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
29	chr5:104757800-104758600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
30	chr5:104763400-104764400	Enhancers	Fetal Intestine Large	intestine
31	chr5:104766000-104767600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
32	chr5:104767600-104768600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
33	chr5:104768600-104769000	Enhancers	iPS-18 Cell Line	embryonic stem cell
34	chr5:104768600-104769200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
35	chr5:104796000-104801800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
36	chr5:104811600-104811800	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr5:104817600-104817800	Enhancers	Liver	Liver
38	chr5:104817800-104818200	Active TSS	Liver	Liver
39	chr5:104820000-104820600	Enhancers	HUES48 Cell Line	embryonic stem cell
40	chr5:104828000-104828600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
41	chr5:104829400-104829600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
42	chr5:104833800-104834200	Enhancers	ES-I3 Cell Line	embryonic stem cell
43	chr5:104833800-104834400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr5:104833800-104834400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
45	chr5:104833800-104834400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
46	chr5:104834000-104834400	Enhancers	HUES64 Cell Line	embryonic stem cell
47	chr5:104834000-104834400	Active TSS	Spleen	Spleen
48	chr5:104834400-104836200	Weak transcription	HUES64 Cell Line	embryonic stem cell
49	chr5:104836200-104837000	Enhancers	HUES64 Cell Line	embryonic stem cell
50	chr5:104836200-104837200	Enhancers	iPS-15b Cell Line	embryonic stem cell

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