Variant report

Variant	nsv1031268
Chromosome Location	chr5:104703437-104800362
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:246)
CpG islands
(count:122)
Chromatin interactive
region (count:24)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:246 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:104728602-104728921	K562	blood:	n/a	n/a
2	ARID3A	chr5:104726542-104727019	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	chr5:104779909-104779930	K562	blood:	n/a	n/a
7	BACH1	chr5:104738330-104738373	K562	blood:	n/a	n/a
8	BHLHE40	chr5:104728493-104728748	K562	blood:	n/a	n/a
9	CBX3	chr5:104728363-104729015	K562	blood:	n/a	n/a
10	CBX3	chr5:104755081-104755354	K562	blood:	n/a	n/a
11	CBX3	chr5:104728451-104728993	K562	blood:	n/a	n/a
12	CBX3	chr5:104796414-104796740	K562	blood:	n/a	n/a
13	CBX3	chr5:104796463-104796676	K562	blood:	n/a	n/a
14	CBX3	chr5:104755037-104755389	K562	blood:	n/a	n/a
15	CCNT2	chr5:104727769-104728552	K562	blood:	n/a	n/a
16	CEBPB	chr5:104709824-104710103	IMR90	lung:	n/a	n/a
17	CEBPB	chr5:104788448-104788780	HepG2	liver:	n/a	chr5:104788606-104788619 chr5:104788606-104788617 chr5:104788603-104788620
18	CEBPB	chr5:104709840-104710114	HepG2	liver:	n/a	n/a
19	CEBPB	chr5:104780741-104780853	K562	blood:	n/a	n/a
20	CEBPB	chr5:104709810-104710130	A549	lung:	n/a	n/a
21	CEBPB	chr5:104720876-104721252	K562	blood:	n/a	n/a
22	CEBPB	chr5:104788546-104788789	A549	lung:	n/a	chr5:104788606-104788619 chr5:104788606-104788617 chr5:104788603-104788620
23	CEBPB	chr5:104783657-104783915	HepG2	liver:	n/a	chr5:104783784-104783795
24	CEBPB	chr5:104709884-104709984	H1-hESC	embryonic stem cell:	n/a	n/a
25	CEBPB	chr5:104720977-104721172	H1-hESC	embryonic stem cell:	n/a	n/a
26	CHD2	chr5:104728384-104728863	K562	blood:	n/a	n/a
27	CHD2	chr5:104727637-104727834	K562	blood:	n/a	n/a
28	CHD2	chr5:104796530-104796598	H1-hESC	embryonic stem cell:	n/a	n/a
29	CTCF	chr5:104797250-104797319	Medullo	brain:	n/a	n/a
30	CTCF	chr5:104787945-104787991	Pancreas_OC	pancreas:	n/a	n/a
31	CTCF	chr5:104727920-104728070	HepG2	liver:	n/a	n/a
32	CTCF	chr5:104789240-104789390	HPF	lung:	n/a	n/a
33	CTCF	chr5:104727909-104728007	K562	blood:	n/a	n/a
34	CUX1	chr5:104726108-104726579	K562	blood:	n/a	n/a
35	CUX1	chr5:104726999-104727199	K562	blood:	n/a	n/a
36	CUX1	chr5:104727561-104727756	K562	blood:	n/a	n/a
37	E2F4	chr5:104752031-104752136	MCF10A-Er-Src	breast:	n/a	n/a
38	E2F4	chr5:104767057-104767257	MCF10A-Er-Src	breast:	n/a	n/a
39	ELF1	chr5:104728575-104728905	HepG2	liver:	n/a	n/a
40	ELF1	chr5:104728448-104729083	HCT-116	colon:	n/a	n/a
41	ELF1	chr5:104728319-104729210	HCT-116	colon:	n/a	n/a
42	ELF1	chr5:104728572-104728937	HepG2	liver:	n/a	n/a
43	ELF1	chr5:104728406-104728965	K562	blood:	n/a	n/a
44	ELF1	chr5:104728044-104728975	K562	blood:	n/a	n/a
45	ELK1	chr5:104728596-104728947	K562	blood:	n/a	n/a
46	EP300	chr5:104724171-104724744	MCF-7	breast:	n/a	n/a
47	EP300	chr5:104728530-104728887	GM12878	blood:	n/a	n/a
48	EP300	chr5:104733154-104733713	MCF-7	breast:	n/a	n/a
49	EP300	chr5:104728503-104728971	K562	blood:	n/a	n/a
50	ESR1	chr5:104724177-104724588	T-47D	breast:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:104728220-104728270	K562	blood:	n/a
2	chr5:104728220-104728270	HCF	heart:	n/a
3	chr5:104728427-104728477	ovcar-3	ovarian:	n/a
4	chr5:104728220-104728270	HCM	heart:	n/a
5	chr5:104728427-104728477	Hepatocyte	liver:	n/a
6	chr5:104728220-104728270	HEK293	kidney:	embryo
7	chr5:104728220-104728270	MCF-7	breast:	n/a
8	chr5:104728220-104728270	NHDF-neo	bronchial:	n/a
9	chr5:104728220-104728270	HIPEpiC	eye:	n/a
10	chr5:104728427-104728477	GM06990	blood:	n/a
11	chr5:104728220-104728270	ECC-1	luminal epithelium:	n/a
12	chr5:104728220-104728270	HRE	kidney:	n/a
13	chr5:104728220-104728270	GM19239	blood:	n/a
14	chr5:104728220-104728270	SK-N-SH_RA	brain:	n/a
15	chr5:104728427-104728477	MCF-7	breast:	n/a
16	chr5:104728427-104728477	RPTEC	kidney:	n/a
17	chr5:104728427-104728477	HCF	heart:	n/a
18	chr5:104728220-104728270	GM12878	blood:	n/a
19	chr5:104728220-104728270	NB4	blood:	n/a
20	chr5:104728220-104728270	RPTEC	kidney:	n/a
21	chr5:104728427-104728477	PFSK-1	brain:	n/a
22	chr5:104728427-104728477	H1-hESC	embryonic stem cell:	embryo
23	chr5:104728220-104728270	PrEC	prostate:	n/a
24	chr5:104728220-104728270	HRCEpiC	kidney:	n/a
25	chr5:104728220-104728270	HUVEC	blood vessel:	n/a
26	chr5:104728427-104728477	HepG2	liver:	n/a
27	chr5:104728427-104728477	GM12891	blood:	n/a
28	chr5:104728427-104728477	HNPCEpiC	eye:	n/a
29	chr5:104728427-104728477	HMEC	breast:	n/a
30	chr5:104728427-104728477	CMK	blood:	n/a
31	chr5:104728427-104728477	SAEC	small airway:	n/a
32	chr5:104728427-104728477	HIPEpiC	eye:	n/a
33	chr5:104728220-104728270	GM12892	blood:	n/a
34	chr5:104728220-104728270	HNPCEpiC	eye:	n/a
35	chr5:104728220-104728270	HL-60	blood:	n/a
36	chr5:104728427-104728477	HPAEpiC	pulmonary alveolar:	n/a
37	chr5:104728427-104728477	HEEpiC	esophagus:	n/a
38	chr5:104728427-104728477	A549	lung:	n/a
39	chr5:104728427-104728477	HAEpiC	amniotic membrane:	n/a
40	chr5:104728427-104728477	HRPEpiC	eye:	n/a
41	chr5:104728427-104728477	GM12892	blood:	n/a
42	chr5:104728427-104728477	AG10803	skin:	n/a
43	chr5:104728427-104728477	AG09309	skin:	n/a
44	chr5:104728427-104728477	U87	brain:	n/a
45	chr5:104728427-104728477	BJ	skin:	n/a
46	chr5:104728427-104728477	MCF10A-Er-Src	breast:	n/a
47	chr5:104728220-104728270	LNCaP	prostate:	n/a
48	chr5:104728427-104728477	HCT-116	colon:	n/a
49	chr5:104728427-104728477	SKMC	muscle:	n/a
50	chr5:104728220-104728270	U87	brain:	n/a

(count:24 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:104712112..104715391-chr5:104727182..104729595,3	K562	blood:
2	chr5:104723018..104724952-chr5:104737690..104739211,2	K562	blood:
3	chr5:104726359..104728666-chr5:105131284..105132821,2	K562	blood:
4	chr5:104711472..104715081-chr5:104725603..104729958,5	K562	blood:
5	chr5:104778136..104780320-chr5:104785388..104787017,2	K562	blood:
6	chr5:104726534..104729492-chr5:107716153..107718681,2	K562	blood:
7	chr5:104727742..104729434-chr5:104763198..104765492,2	K562	blood:
8	chr5:104710520..104712024-chr5:104741469..104744150,2	K562	blood:
9	chr1:184434764..184435543-chr5:104792004..104792524,3	MCF-7	breast:
10	chr5:104740786..104743331-chr5:104745586..104748363,2	K562	blood:
11	chr5:104710520..104712024-chr5:104741469..104744150,2	K562	blood:
12	chr5:104778136..104780320-chr5:104785388..104787017,2	K562	blood:
13	chr5:104768629..104770858-chr5:104785097..104787270,2	K562	blood:
14	chr5:104679097..104680828-chr5:104708980..104711591,2	K562	blood:
15	chr5:104729079..104730844-chr5:104733038..104734650,2	K562	blood:
16	chr5:104740786..104743331-chr5:104745586..104748363,2	K562	blood:
17	chr5:104768629..104770858-chr5:104785097..104787270,2	K562	blood:
18	chr5:104722652..104724763-chr5:104741861..104743629,2	K562	blood:
19	chr5:104729079..104730844-chr5:104733038..104734650,2	K562	blood:
20	chr5:104733236..104736068-chr5:104886596..104888346,2	MCF-7	breast:
21	chr5:104723018..104724952-chr5:104737690..104739211,2	K562	blood:
22	chr5:104716167..104718489-chr5:104728063..104729895,2	K562	blood:
23	chr5:104727296..104728816-chr5:104790778..104793743,2	K562	blood:
24	chr5:104722652..104724763-chr5:104741861..104743629,2	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
ENSG00000145743	chromatin interactions
ENSG00000251574	chromatin interactions

Extended variants
information (count: 1181 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:1181 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs572852384	chr5:104711479-104711480	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs34187588	chr5:104711508-104711509	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs183608763	chr5:104711509-104711510	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs368440026	chr5:104711595-104711596	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs565404341	chr5:104711609-104711610	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs144304228	chr5:104711613-104711614	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs186791670	chr5:104711636-104711637	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs372093894	chr5:104711669-104711670	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs561155541	chr5:104711670-104711671	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs112854342	chr5:104711675-104711676	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs546686664	chr5:104711694-104711695	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs55921119	chr5:104711744-104711745	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs3072400	chr5:104711748-104711749	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs70993936	chr5:104711749-104711750	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs560241642	chr5:104711781-104711782	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs532388295	chr5:104711870-104711871	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs374103326	chr5:104711922-104711923	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs552559385	chr5:104711934-104711935	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs546207518	chr5:104711958-104711959	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs111624212	chr5:104711978-104711979	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs113702336	chr5:104711979-104711980	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs571425613	chr5:104711998-104711999	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs191508958	chr5:104711999-104712000	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs527577405	chr5:104712012-104712013	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs540147574	chr5:104712070-104712071	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs184887660	chr5:104712132-104712133	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs189867332	chr5:104712166-104712167	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs567463342	chr5:104712169-104712170	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs141439570	chr5:104712209-104712210	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs553087336	chr5:104712315-104712316	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs182028066	chr5:104712428-104712429	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs534851059	chr5:104712434-104712435	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs367552907	chr5:104712441-104712442	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs538227550	chr5:104712446-104712447	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs539652080	chr5:104712467-104712468	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs150576350	chr5:104712484-104712485	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs575807851	chr5:104712552-104712553	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs558751625	chr5:104712566-104712567	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs185315822	chr5:104712572-104712573	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs139976619	chr5:104712588-104712589	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs559558871	chr5:104712607-104712608	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs116477557	chr5:104712651-104712652	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs189393010	chr5:104712654-104712655	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs113762172	chr5:104712662-104712663	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs143337067	chr5:104712679-104712680	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs562913907	chr5:104712716-104712717	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs146731383	chr5:104712731-104712732	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs182087423	chr5:104712735-104712736	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs550870108	chr5:104712740-104712741	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs567597945	chr5:104712785-104712786	Inactive region	Chromatin interactive region	1 gene(s)	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:36 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:104715600-104716800	Enhancers	Fetal Brain Male	brain
2	chr5:104722000-104722200	Enhancers	HUES48 Cell Line	embryonic stem cell
3	chr5:104722200-104722600	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
4	chr5:104722200-104722800	Enhancers	HUES6 Cell Line	embryonic stem cell
5	chr5:104722200-104723200	Enhancers	HUES64 Cell Line	embryonic stem cell
6	chr5:104722400-104723400	Enhancers	iPS-15b Cell Line	embryonic stem cell
7	chr5:104722400-104723600	Enhancers	ES-I3 Cell Line	embryonic stem cell
8	chr5:104722600-104723000	Enhancers	HUES48 Cell Line	embryonic stem cell
9	chr5:104724800-104725800	Enhancers	K562	blood
10	chr5:104725800-104726400	Weak transcription	K562	blood
11	chr5:104726400-104729200	Active TSS	K562	blood
12	chr5:104727400-104727600	Enhancers	Placenta	Placenta
13	chr5:104727600-104727800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
14	chr5:104727600-104728000	Flanking Active TSS	Placenta	Placenta
15	chr5:104727600-104729000	Active TSS	HepG2	liver
16	chr5:104727800-104728000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr5:104727800-104728600	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
18	chr5:104728000-104728400	Active TSS	Placenta	Placenta
19	chr5:104728400-104728800	ZNF genes & repeats	Placenta	Placenta
20	chr5:104742400-104743400	Enhancers	HUES48 Cell Line	embryonic stem cell
21	chr5:104742400-104743600	Enhancers	HUES64 Cell Line	embryonic stem cell
22	chr5:104742400-104743600	Enhancers	iPS-15b Cell Line	embryonic stem cell
23	chr5:104742600-104743400	Enhancers	ES-I3 Cell Line	embryonic stem cell
24	chr5:104742800-104743200	Enhancers	HUES6 Cell Line	embryonic stem cell
25	chr5:104742800-104743400	Enhancers	iPS-18 Cell Line	embryonic stem cell
26	chr5:104748600-104749200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
27	chr5:104748800-104749200	Enhancers	HUES6 Cell Line	embryonic stem cell
28	chr5:104749200-104749600	Bivalent Enhancer	Placenta	Placenta
29	chr5:104749200-104749800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
30	chr5:104757800-104758600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
31	chr5:104763400-104764400	Enhancers	Fetal Intestine Large	intestine
32	chr5:104766000-104767600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
33	chr5:104767600-104768600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
34	chr5:104768600-104769000	Enhancers	iPS-18 Cell Line	embryonic stem cell
35	chr5:104768600-104769200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
36	chr5:104796000-104801800	Weak transcription	ES-I3 Cell Line	embryonic stem cell

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