Variant report

Variant	nsv591158
Chromosome Location	chr3:100345201-100410724
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:743)
CpG islands
(count:244)
Chromatin interactive
region (count:26)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:743 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:100369723-100370159	K562	blood:	n/a	n/a
2	ARID3A	chr3:100353734-100354533	HepG2	liver:	n/a	n/a
3	ARID3A	chr3:100400484-100400645	HepG2	liver:	n/a	n/a
4	ARID3A	chr3:100359648-100359874	HepG2	liver:	n/a	n/a
5	ARID3A	chr3:100348388-100349223	K562	blood:	n/a	n/a
6	ARID3A	chr3:100381238-100381404	K562	blood:	n/a	n/a
7	ARID3A	chr3:100353731-100353930	K562	blood:	n/a	n/a
8	ATF1	chr3:100353718-100353993	K562	blood:	n/a	n/a
9	ATF1	chr3:100348373-100348950	K562	blood:	n/a	n/a
10	ATF2	chr3:100369506-100370238	GM12878	blood:	n/a	n/a
11	ATF2	chr3:100360476-100360923	GM12878	blood:	n/a	n/a
12	ATF3	chr3:100370050-100370425	K562	blood:	n/a	n/a
13	ATF3	chr3:100348592-100348961	K562	blood:	n/a	n/a
14	BACH1	chr3:100381410-100381594	K562	blood:	n/a	n/a
15	BACH1	chr3:100349457-100349877	H1-hESC	embryonic stem cell:	n/a	chr3:100349697-100349711
16	BATF	chr3:100360218-100360885	GM12878	blood:	n/a	chr3:100360555-100360566
17	BATF	chr3:100369685-100370004	GM12878	blood:	n/a	n/a
18	BATF	chr3:100369687-100370030	GM12878	blood:	n/a	n/a
19	BATF	chr3:100360240-100360471	GM12878	blood:	n/a	n/a
20	BCL11A	chr3:100360235-100360494	GM12878	blood:	n/a	n/a
21	BCL11A	chr3:100360195-100360894	GM12878	blood:	n/a	n/a
22	BCL11A	chr3:100360611-100360835	GM12878	blood:	n/a	n/a
23	BHLHE40	chr3:100353702-100354034	K562	blood:	n/a	n/a
24	BHLHE40	chr3:100353728-100354019	HepG2	liver:	n/a	n/a
25	BHLHE40	chr3:100369647-100370331	GM12878	blood:	n/a	n/a
26	BHLHE40	chr3:100353686-100354022	GM12878	blood:	n/a	n/a
27	BHLHE40	chr3:100360142-100360910	GM12878	blood:	n/a	n/a
28	CCNT2	chr3:100348632-100349219	K562	blood:	n/a	n/a
29	CEBPB	chr3:100348561-100348881	K562	blood:	n/a	n/a
30	CEBPB	chr3:100381321-100381668	Hela-S3	cervix:	n/a	n/a
31	CEBPB	chr3:100385548-100385946	K562	blood:	n/a	chr3:100385738-100385749
32	CEBPB	chr3:100350095-100350440	Hela-S3	cervix:	n/a	n/a
33	CEBPB	chr3:100370681-100370966	K562	blood:	n/a	n/a
34	CEBPB	chr3:100385583-100385925	H1-hESC	embryonic stem cell:	n/a	chr3:100385738-100385749
35	CEBPB	chr3:100384545-100384598	K562	blood:	n/a	chr3:100384580-100384591
36	CEBPB	chr3:100370681-100370923	A549	lung:	n/a	n/a
37	CEBPB	chr3:100370210-100370426	A549	lung:	n/a	chr3:100370349-100370362
38	CEBPB	chr3:100385579-100385925	Hela-S3	cervix:	n/a	chr3:100385738-100385749
39	CEBPB	chr3:100400369-100400703	HepG2	liver:	n/a	n/a
40	CEBPB	chr3:100385592-100385797	K562	blood:	n/a	chr3:100385738-100385749
41	CEBPB	chr3:100373432-100373699	A549	lung:	n/a	chr3:100373575-100373586
42	CEBPB	chr3:100353821-100353823	Hela-S3	cervix:	n/a	n/a
43	CEBPB	chr3:100385560-100385922	IMR90	lung:	n/a	chr3:100385738-100385749
44	CEBPB	chr3:100370096-100370525	Hela-S3	cervix:	n/a	chr3:100370349-100370362
45	CEBPB	chr3:100373411-100373726	HepG2	liver:	n/a	chr3:100373575-100373586
46	CEBPB	chr3:100370030-100370435	HCT-116	colon:	n/a	chr3:100370349-100370362
47	CEBPB	chr3:100385561-100385931	A549	lung:	n/a	chr3:100385738-100385749
48	CEBPB	chr3:100370097-100370487	IMR90	lung:	n/a	chr3:100370349-100370362
49	CEBPB	chr3:100381066-100381689	K562	blood:	n/a	n/a
50	CEBPB	chr3:100373450-100373663	K562	blood:	n/a	chr3:100373575-100373586

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:100401270-100401320	HNPCEpiC	eye:	n/a
2	chr3:100401284-100401334	HPAEpiC	pulmonary alveolar:	n/a
3	chr3:100401284-100401334	SKMC	muscle:	n/a
4	chr3:100349374-100349424	HCM	heart:	n/a
5	chr3:100401270-100401320	HEEpiC	esophagus:	n/a
6	chr3:100401284-100401334	Jurkat	blood:	n/a
7	chr3:100401200-100401250	ProgFib	skin:	n/a
8	chr3:100349374-100349424	HNPCEpiC	eye:	n/a
9	chr3:100401200-100401250	MCF-7	breast:	n/a
10	chr3:100349374-100349424	H1-hESC	embryonic stem cell:	embryo
11	chr3:100401200-100401250	Caco-2	colon:	n/a
12	chr3:100401270-100401320	MCF10A-Er-Src	breast:	n/a
13	chr3:100401200-100401250	Hela-S3	cervix:	n/a
14	chr3:100349374-100349424	AG04450	lung:	fetal
15	chr3:100349374-100349424	A549	lung:	n/a
16	chr3:100401270-100401320	H1-hESC	embryonic stem cell:	embryo
17	chr3:100349374-100349424	BJ	skin:	n/a
18	chr3:100401270-100401320	HPAEpiC	pulmonary alveolar:	n/a
19	chr3:100349374-100349424	GM12892	blood:	n/a
20	chr3:100401284-100401334	T-47D	breast:	n/a
21	chr3:100401284-100401334	SAEC	small airway:	n/a
22	chr3:100401200-100401250	CMK	blood:	n/a
23	chr3:100401200-100401250	NHDF-neo	bronchial:	n/a
24	chr3:100401200-100401250	AoSMC	blood vessel:	n/a
25	chr3:100401270-100401320	NH-A	brain:	n/a
26	chr3:100401284-100401334	AG09319	gingival:	n/a
27	chr3:100401270-100401320	Hepatocyte	liver:	n/a
28	chr3:100401270-100401320	K562	blood:	n/a
29	chr3:100349374-100349424	Caco-2	colon:	n/a
30	chr3:100349374-100349424	HPAEpiC	pulmonary alveolar:	n/a
31	chr3:100401284-100401334	HepG2	liver:	n/a
32	chr3:100349374-100349424	SK-N-SH_RA	brain:	n/a
33	chr3:100401284-100401334	PFSK-1	brain:	n/a
34	chr3:100401200-100401250	AG10803	skin:	n/a
35	chr3:100401284-100401334	PANC-1	pancreas:	n/a
36	chr3:100401284-100401334	SK-N-SH	brain:	n/a
37	chr3:100349374-100349424	NH-A	brain:	n/a
38	chr3:100401200-100401250	BE2_C	brain:	n/a
39	chr3:100401284-100401334	HCT-116	colon:	n/a
40	chr3:100401200-100401250	AG09309	skin:	n/a
41	chr3:100401200-100401250	ECC-1	luminal epithelium:	n/a
42	chr3:100401284-100401334	LNCaP	prostate:	n/a
43	chr3:100401200-100401250	HMEC	breast:	n/a
44	chr3:100401284-100401334	U87	brain:	n/a
45	chr3:100401200-100401250	MCF10A-Er-Src	breast:	n/a
46	chr3:100401200-100401250	SK-N-SH_RA	brain:	n/a
47	chr3:100349374-100349424	HepG2	liver:	n/a
48	chr3:100401200-100401250	SK-N-MC	brain:	n/a
49	chr3:100401284-100401334	AG10803	skin:	n/a
50	chr3:100401200-100401250	HIPEpiC	eye:	n/a

(count:26 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:100322114..100322780-chr3:100353316..100353989,3	MCF-7	breast:
2	chr3:100353552..100356244-chr3:100358458..100360777,2	K562	blood:
3	chr3:100374838..100376761-chr3:100378684..100380359,2	K562	blood:
4	chr3:100348848..100350394-chr3:100351417..100354134,2	K562	blood:
5	chr3:100369607..100371401-chr3:100374454..100376110,2	K562	blood:
6	chr3:100410212..100413199-chr3:100413505..100415346,2	K562	blood:
7	chr3:100369607..100371401-chr3:100374454..100376110,2	K562	blood:
8	chr3:100348848..100350394-chr3:100351417..100354134,2	K562	blood:
9	chr3:100181153..100182757-chr3:100352927..100354311,7	MCF-7	breast:
10	chr3:100355413..100357441-chr3:100427541..100429664,2	K562	blood:
11	chr3:100321992..100322818-chr3:100353419..100354308,2	MCF-7	breast:
12	chr3:100348848..100350778-chr3:100351417..100355406,3	K562	blood:
13	chr3:100120818..100123698-chr3:100370041..100372201,2	K562	blood:
14	chr3:100340717..100343040-chr3:100348395..100351881,3	K562	blood:
15	chr3:100118924..100121912-chr3:100362623..100364573,2	K562	blood:
16	chr3:100181696..100182432-chr3:100355242..100355805,2	MCF-7	breast:
17	chr3:100358087..100360713-chr3:100362813..100364716,2	K562	blood:
18	chr3:100358087..100360713-chr3:100362813..100364716,2	K562	blood:
19	chr3:100120411..100122999-chr3:100364924..100367578,2	K562	blood:
20	chr3:100367436..100369530-chr3:100426605..100429472,2	MCF-7	breast:
21	chr3:100325407..100326196-chr3:100353394..100354270,2	MCF-7	breast:
22	chr3:100374838..100376761-chr3:100378684..100380359,2	K562	blood:
23	chr3:100325466..100327241-chr3:100349090..100350621,2	K562	blood:
24	chr3:100364940..100366707-chr3:100366782..100369483,3	K562	blood:
25	chr3:100321003..100323549-chr3:100347554..100350487,3	MCF-7	breast:
26	chr3:100372478..100376338-chr3:100378859..100382078,3	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ABI3BP-1	chr3:100383894-100384320	NONHSAT090876
2	lnc-TMEM45A-1	chr3:100354384-100354670	NONHSAT090874
3	lnc-TMEM45A-1	chr3:100356146-100356419	NONHSAT090874

No data

Variant related genes	Relation type
GPR128	TF binding region
ENSG00000252989	TF binding region
GMFBP1	TF binding region
GPR128	CpG island
ENSG00000252989	CpG island
GMFBP1	CpG island
ENSG00000154174	chromatin interactions
ENSG00000144820	chromatin interactions
ENSG00000114354	chromatin interactions
ENSG00000206535	chromatin interactions
ENSG00000252989	chromatin interactions

Extended variants
information (count: 2726 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:2726 , 50 per page) page: 1 2 3 4 5 6 7 ... 55

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1165253	chr3:100345201-100345202	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs550074229	chr3:100345219-100345220	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs534998327	chr3:100345228-100345229	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs187606850	chr3:100345252-100345253	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs374807900	chr3:100345295-100345296	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs116774509	chr3:100345299-100345300	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs370108402	chr3:100345347-100345348	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs557525654	chr3:100345356-100345357	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs138150413	chr3:100345427-100345428	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs191722616	chr3:100345458-100345459	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs202016857	chr3:100345468-100345469	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs555369073	chr3:100345490-100345491	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs573838180	chr3:100345493-100345494	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs184340159	chr3:100345496-100345497	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs562774521	chr3:100345575-100345576	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs577872124	chr3:100345578-100345579	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs114856359	chr3:100345623-100345624	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs141097288	chr3:100345679-100345680	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs144820461	chr3:100345712-100345713	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs528078523	chr3:100345746-100345747	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs549095934	chr3:100345825-100345826	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs546636032	chr3:100345826-100345827	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs561304313	chr3:100345849-100345850	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs531616210	chr3:100345857-100345858	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs550012657	chr3:100345879-100345880	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs188107456	chr3:100345886-100345887	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs192363175	chr3:100345896-100345897	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs538836234	chr3:100345916-100345917	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs73143198	chr3:100345918-100345919	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs185560140	chr3:100345956-100345957	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs77878285	chr3:100345994-100345995	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs555186481	chr3:100346009-100346010	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs567224749	chr3:100346028-100346029	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs537851231	chr3:100346070-100346071	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs118187612	chr3:100346135-100346136	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs190483813	chr3:100346153-100346154	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs182504521	chr3:100346158-100346159	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs629967	chr3:100346247-100346248	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs185814842	chr3:100346322-100346323	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs543077296	chr3:100346334-100346335	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs569428467	chr3:100346346-100346347	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs561226567	chr3:100346361-100346362	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs138664702	chr3:100346388-100346389	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs141232715	chr3:100346401-100346402	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs629091	chr3:100346412-100346413	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs573015201	chr3:100346443-100346444	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs532693940	chr3:100346497-100346498	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs189087674	chr3:100346504-100346505	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs566229838	chr3:100346515-100346516	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs150747605	chr3:100346599-100346600	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:59)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
Renal cell carcinoma	21668985	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Hirschsprung''s Disease	21712996	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	21183584	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Bipolar disorder	20877625	CNVD
Bipolar disorder	21956041	CNVD
Bipolar disorder	22241247	CNVD
Biliary cancer	18923514	CNVD
Prostate cancer	21965145	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Cervical cancer	21062161	CNVD
Squamous cell cancer	20885788	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Bipolar disorder	18458673	CNVD
Breast cancer	22032731	CNVD
Neurodevelopmental disorder	22521361	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Breast cancer	16461572	CNVD
Neuroblastoma	17533364	CNVD
microdeletion syndrome	22180640	CNVD
Cervical Cancer	21857958	CNVD
Melanoma	21693616	CNVD
Lung cancer	21426551	CNVD
Cancer	21637783	CNVD
Cervical cancer	21063398	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oral cancer	21386901	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	22065749	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
small cell lung cancer	20016488	CNVD
Ductal carcinoma	22052326	CNVD
Myelofibrosis	22110671	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Breast cancer	16608533	CNVD
Breast cancer	21785460	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD

Chromatin state (count:396 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:100343800-100352000	Weak transcription	Fetal Intestine Large	intestine
2	chr3:100346200-100348000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr3:100346400-100348200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
4	chr3:100347400-100347600	Enhancers	Small Intestine	intestine
5	chr3:100347400-100348600	Enhancers	Primary hematopoietic stem cells	blood
6	chr3:100347600-100349200	Weak transcription	Small Intestine	intestine
7	chr3:100347600-100350000	Enhancers	HUVEC	blood vessel
8	chr3:100347600-100350400	Enhancers	K562	blood
9	chr3:100347800-100349800	Enhancers	Primary hematopoietic stem cells short term culture	blood
10	chr3:100348000-100348800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr3:100348200-100348600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
12	chr3:100348200-100349800	Enhancers	NHEK	skin
13	chr3:100348200-100352200	Weak transcription	Primary neutrophils fromperipheralblood	blood
14	chr3:100348400-100349200	Enhancers	Duodenum Mucosa	Duodenum
15	chr3:100348400-100349400	Enhancers	Fetal Intestine Small	intestine
16	chr3:100348400-100350600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
17	chr3:100348400-100350600	Enhancers	HMEC	breast
18	chr3:100348600-100349800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
19	chr3:100348600-100350200	Enhancers	Hela-S3	cervix
20	chr3:100348600-100350400	Enhancers	HUES64 Cell Line	embryonic stem cell
21	chr3:100348600-100353400	Weak transcription	Primary hematopoietic stem cells	blood
22	chr3:100348600-100354200	Weak transcription	Sigmoid Colon	Sigmoid Colon
23	chr3:100348800-100349800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr3:100349000-100350400	Enhancers	iPS-15b Cell Line	embryonic stem cell
25	chr3:100349000-100350600	Enhancers	ES-I3 Cell Line	embryonic stem cell
26	chr3:100349000-100350600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
27	chr3:100349200-100349400	Enhancers	Small Intestine	intestine
28	chr3:100349200-100350200	Enhancers	A549	lung
29	chr3:100349200-100350400	Enhancers	HUES6 Cell Line	embryonic stem cell
30	chr3:100349200-100350400	Enhancers	iPS-18 Cell Line	embryonic stem cell
31	chr3:100349200-100350600	Enhancers	iPS-20b Cell Line	embryonic stem cell
32	chr3:100349200-100352400	Weak transcription	Duodenum Mucosa	Duodenum
33	chr3:100349400-100352800	Weak transcription	Fetal Intestine Small	intestine
34	chr3:100349600-100349800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr3:100349600-100349800	Bivalent Enhancer	NHDF-Ad	bronchial
36	chr3:100349600-100350400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
37	chr3:100349600-100350400	Enhancers	H9 Cell Line	embryonic stem cell
38	chr3:100349800-100350000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr3:100349800-100352600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
40	chr3:100349800-100352800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
41	chr3:100349800-100352800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr3:100350400-100353600	Weak transcription	K562	blood
43	chr3:100350600-100353600	Weak transcription	HMEC	breast
44	chr3:100350600-100354000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
45	chr3:100352000-100353000	Strong transcription	Fetal Intestine Large	intestine
46	chr3:100352200-100353800	Strong transcription	Primary neutrophils fromperipheralblood	blood
47	chr3:100352400-100353000	Strong transcription	Duodenum Mucosa	Duodenum
48	chr3:100352600-100354600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
49	chr3:100352800-100353400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
50	chr3:100352800-100354000	Enhancers	Primary hematopoietic stem cells short term culture	blood

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