Variant report

Variant	nsv432467
Chromosome Location	chr3:100342310-100442310
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1736)
CpG islands
(count:1221)
Chromatin interactive
region (count:69)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1736 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:100359648-100359874	HepG2	liver:	n/a	n/a
2	ARID3A	chr3:100348388-100349223	K562	blood:	n/a	n/a
3	ARID3A	chr3:100353731-100353930	K562	blood:	n/a	n/a
4	ARID3A	chr3:100400484-100400645	HepG2	liver:	n/a	n/a
5	ARID3A	chr3:100428405-100428550	K562	blood:	n/a	n/a
6	ARID3A	chr3:100369723-100370159	K562	blood:	n/a	n/a
7	ARID3A	chr3:100353734-100354533	HepG2	liver:	n/a	n/a
8	ARID3A	chr3:100427756-100428585	HepG2	liver:	n/a	n/a
9	ARID3A	chr3:100381238-100381404	K562	blood:	n/a	n/a
10	ATF1	chr3:100427978-100428440	K562	blood:	n/a	n/a
11	ATF1	chr3:100348373-100348950	K562	blood:	n/a	n/a
12	ATF1	chr3:100353718-100353993	K562	blood:	n/a	n/a
13	ATF2	chr3:100427777-100428567	GM12878	blood:	n/a	n/a
14	ATF2	chr3:100369506-100370238	GM12878	blood:	n/a	n/a
15	ATF2	chr3:100429275-100429952	GM12878	blood:	n/a	n/a
16	ATF2	chr3:100360476-100360923	GM12878	blood:	n/a	n/a
17	ATF3	chr3:100348592-100348961	K562	blood:	n/a	n/a
18	ATF3	chr3:100370050-100370425	K562	blood:	n/a	n/a
19	BACH1	chr3:100349457-100349877	H1-hESC	embryonic stem cell:	n/a	chr3:100349697-100349711
20	BACH1	chr3:100421524-100421801	H1-hESC	embryonic stem cell:	n/a	n/a
21	BACH1	chr3:100381410-100381594	K562	blood:	n/a	n/a
22	BACH1	chr3:100428023-100428678	H1-hESC	embryonic stem cell:	n/a	n/a
23	BACH1	chr3:100421452-100421833	K562	blood:	n/a	n/a
24	BATF	chr3:100369687-100370030	GM12878	blood:	n/a	n/a
25	BATF	chr3:100429333-100429812	GM12878	blood:	n/a	n/a
26	BATF	chr3:100360240-100360471	GM12878	blood:	n/a	n/a
27	BATF	chr3:100429220-100429801	GM12878	blood:	n/a	n/a
28	BATF	chr3:100369685-100370004	GM12878	blood:	n/a	n/a
29	BATF	chr3:100360218-100360885	GM12878	blood:	n/a	chr3:100360555-100360566
30	BCL11A	chr3:100360195-100360894	GM12878	blood:	n/a	n/a
31	BCL11A	chr3:100360611-100360835	GM12878	blood:	n/a	n/a
32	BCL11A	chr3:100360235-100360494	GM12878	blood:	n/a	n/a
33	BCLAF1	chr3:100429350-100429879	GM12878	blood:	n/a	chr3:100429694-100429703 chr3:100429744-100429753 chr3:100429743-100429752
34	BCLAF1	chr3:100428169-100428667	GM12878	blood:	n/a	chr3:100428545-100428558 chr3:100428541-100428554 chr3:100428539-100428552
35	BHLHE40	chr3:100427985-100428525	K562	blood:	n/a	n/a
36	BHLHE40	chr3:100353728-100354019	HepG2	liver:	n/a	n/a
37	BHLHE40	chr3:100360142-100360910	GM12878	blood:	n/a	n/a
38	BHLHE40	chr3:100428011-100428266	A549	lung:	n/a	n/a
39	BHLHE40	chr3:100427970-100428628	HepG2	liver:	n/a	chr3:100428533-100428549
40	BHLHE40	chr3:100427893-100428554	GM12878	blood:	n/a	chr3:100428533-100428549
41	BHLHE40	chr3:100353686-100354022	GM12878	blood:	n/a	n/a
42	BHLHE40	chr3:100369647-100370331	GM12878	blood:	n/a	n/a
43	BHLHE40	chr3:100428885-100428960	K562	blood:	n/a	n/a
44	BHLHE40	chr3:100353702-100354034	K562	blood:	n/a	n/a
45	BRCA1	chr3:100427866-100428531	GM12878	blood:	n/a	n/a
46	BRCA1	chr3:100429415-100429752	Hela-S3	cervix:	n/a	n/a
47	BRCA1	chr3:100428898-100429175	H1-hESC	embryonic stem cell:	n/a	n/a
48	BRCA1	chr3:100427800-100428582	H1-hESC	embryonic stem cell:	n/a	n/a
49	BRCA1	chr3:100428290-100428586	HepG2	liver:	n/a	n/a
50	BRCA1	chr3:100427676-100428558	Hela-S3	cervix:	n/a	n/a

(count:1221 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:100427096-100427146	HUVEC	blood vessel:	n/a
2	chr3:100427096-100427146	HUVEC	blood vessel:	n/a
3	chr3:100427096-100427146	NT2-D1	testis:	n/a
4	chr3:100349374-100349424	HepG2	liver:	n/a
5	chr3:100437347-100437397	NT2-D1	testis:	n/a
6	chr3:100428140-100428190	GM19239	blood:	n/a
7	chr3:100428033-100428083	SK-N-SH_RA	brain:	n/a
8	chr3:100430811-100430861	AG04450	lung:	fetal
9	chr3:100428398-100428448	HRPEpiC	eye:	n/a
10	chr3:100428005-100428055	GM12891	blood:	n/a
11	chr3:100429064-100429114	SKMC	muscle:	n/a
12	chr3:100401270-100401320	NT2-D1	testis:	n/a
13	chr3:100427239-100427289	ProgFib	skin:	n/a
14	chr3:100429064-100429114	PANC-1	pancreas:	n/a
15	chr3:100427096-100427146	ovcar-3	ovarian:	n/a
16	chr3:100437347-100437397	NHBE	bronchial:	n/a
17	chr3:100401284-100401334	GM06990	blood:	n/a
18	chr3:100429064-100429114	NH-A	brain:	n/a
19	chr3:100428869-100428919	BJ	skin:	n/a
20	chr3:100428140-100428190	LNCaP	prostate:	n/a
21	chr3:100427239-100427289	HEEpiC	esophagus:	n/a
22	chr3:100428642-100428692	AG10803	skin:	n/a
23	chr3:100428145-100428195	HPAEpiC	pulmonary alveolar:	n/a
24	chr3:100427096-100427146	IMR90	lung:	fetal
25	chr3:100427096-100427146	MCF-7	breast:	n/a
26	chr3:100428145-100428195	HCM	heart:	n/a
27	chr3:100401270-100401320	HepG2	liver:	n/a
28	chr3:100401200-100401250	ECC-1	luminal epithelium:	n/a
29	chr3:100401200-100401250	NB4	blood:	n/a
30	chr3:100427096-100427146	AG09319	gingival:	n/a
31	chr3:100427096-100427146	U87	brain:	n/a
32	chr3:100428869-100428919	SAEC	small airway:	n/a
33	chr3:100437347-100437397	SKMC	muscle:	n/a
34	chr3:100428033-100428083	A549	lung:	n/a
35	chr3:100401284-100401334	HEEpiC	esophagus:	n/a
36	chr3:100428033-100428083	HCT-116	colon:	n/a
37	chr3:100349374-100349424	ECC-1	luminal epithelium:	n/a
38	chr3:100427239-100427289	GM12878	blood:	n/a
39	chr3:100428145-100428195	AG04449	skin:	fetal
40	chr3:100401284-100401334	BE2_C	brain:	n/a
41	chr3:100428070-100428120	NB4	blood:	n/a
42	chr3:100401284-100401334	SK-N-SH_RA	brain:	n/a
43	chr3:100424830-100424880	AG04449	skin:	fetal
44	chr3:100428398-100428448	K562	blood:	n/a
45	chr3:100428145-100428195	K562	blood:	n/a
46	chr3:100428070-100428120	AG04450	lung:	fetal
47	chr3:100437347-100437397	CMK	blood:	n/a
48	chr3:100428642-100428692	HRPEpiC	eye:	n/a
49	chr3:100428145-100428195	GM19239	blood:	n/a
50	chr3:100428140-100428190	NHDF-neo	bronchial:	n/a

(count:69 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr3:100181696..100182432-chr3:100355242..100355805,2	MCF-7	breast:
2	chr3:100415596..100419109-chr3:100421112..100424187,4	K562	blood:
3	chr1:73273811..73275334-chr3:100425817..100428133,2	MCF-7	breast:
4	chr3:100432153..100434876-chr3:100437236..100438974,2	MCF-7	breast:
5	chr3:100414154..100421316-chr3:100422241..100429195,9	MCF-7	breast:
6	chr3:100425991..100429784-chr3:100429994..100431694,4	K562	blood:
7	chr3:100432153..100434876-chr3:100437236..100438974,2	MCF-7	breast:
8	chr3:99535346..99537040-chr3:100436340..100438429,2	K562	blood:
9	chr3:100355413..100357441-chr3:100427541..100429664,2	K562	blood:
10	chr11:59436077..59436715-chr3:100428082..100428818,2	Hela-S3	cervix:
11	chr3:100374838..100376761-chr3:100378684..100380359,2	K562	blood:
12	chr3:100367436..100369530-chr3:100426605..100429472,2	MCF-7	breast:
13	chr3:100372478..100376338-chr3:100378859..100382078,3	K562	blood:
14	chr3:100427232..100427732-chr9:96215167..96215670,2	Hela-S3	cervix:
15	chr3:100325886..100329093-chr3:100426560..100431642,4	MCF-7	breast:
16	chr3:100423356..100425214-chr3:100428038..100429852,2	K562	blood:
17	chr3:100374838..100376761-chr3:100378684..100380359,2	K562	blood:
18	chr3:100369607..100371401-chr3:100374454..100376110,2	K562	blood:
19	chr3:100420077..100423053-chr3:100428087..100429810,2	MCF-7	breast:
20	chr3:100279818..100281392-chr3:100419411..100421780,2	K562	blood:
21	chr3:100432846..100436544-chr3:100436912..100439975,5	K562	blood:
22	chr3:100428095..100432338-chr3:100432996..100435628,5	K562	blood:
23	chr1:151512640..151513443-chr3:100428519..100429048,2	Hela-S3	cervix:
24	chr3:100352243..100354477-chr3:100424707..100427239,2	MCF-7	breast:
25	chr3:100415596..100419109-chr3:100421112..100424187,4	K562	blood:
26	chr3:100412832..100415800-chr3:100417725..100420372,2	K562	blood:
27	chr17:57918588..57920867-chr3:100426772..100429347,2	MCF-7	breast:
28	chr3:100120818..100123698-chr3:100370041..100372201,2	K562	blood:
29	chr3:100421148..100423017-chr3:100443429..100446212,2	K562	blood:
30	chr3:100325407..100326196-chr3:100353394..100354270,2	MCF-7	breast:
31	chr12:56435446..56435990-chr3:100428103..100428866,2	Hela-S3	cervix:
32	chr3:100428169..100430169-chr3:100436770..100441506,6	MCF-7	breast:
33	chr3:100340717..100343040-chr3:100348395..100351881,3	K562	blood:
34	chr3:100325466..100327241-chr3:100349090..100350621,2	K562	blood:
35	chr3:100428105..100429880-chr3:100429992..100431694,2	K562	blood:
36	chr3:100181153..100182757-chr3:100352927..100354311,7	MCF-7	breast:
37	chr2:67550820..67551820-chr3:100427957..100428561,3	HCT-116	colon:
38	chr18:3247419..3248282-chr3:100427656..100428171,2	Hela-S3	cervix:
39	chr3:100358087..100360713-chr3:100362813..100364716,2	K562	blood:
40	chr3:100118702..100121299-chr3:100427057..100432444,4	K562	blood:
41	chr3:100427539..100430990-chr3:100441684..100444095,3	MCF-7	breast:
42	chr3:100353552..100356244-chr3:100358458..100360777,2	K562	blood:
43	chr20:33543190..33544135-chr3:100427443..100428252,2	NB4	blood:
44	chr3:100412832..100415800-chr3:100417725..100420372,2	K562	blood:
45	chr3:100437193..100438903-chr3:100441910..100444444,2	K562	blood:
46	chr3:100321992..100322818-chr3:100353419..100354308,2	MCF-7	breast:
47	chr3:100410212..100413199-chr3:100413505..100415346,2	K562	blood:
48	chr3:100120411..100122999-chr3:100364924..100367578,2	K562	blood:
49	chr3:100348848..100350778-chr3:100351417..100355406,3	K562	blood:
50	chr3:100118924..100121912-chr3:100362623..100364573,2	K562	blood:

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

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

No data

Variant related genes	Relation type
TFG	TF binding region
GPR128	TF binding region
ENSG00000252989	TF binding region
GMFBP1	TF binding region
TFG	CpG island
GPR128	CpG island
ENSG00000252989	CpG island
GMFBP1	CpG island
ENSG00000144820	chromatin interactions
ENSG00000143367	chromatin interactions
ENSG00000197728	chromatin interactions
ENSG00000184220	chromatin interactions
ENSG00000114354	chromatin interactions
ENSG00000166889	chromatin interactions
ENSG00000188938	chromatin interactions
ENSG00000257449	chromatin interactions
ENSG00000199004	chromatin interactions
ENSG00000206535	chromatin interactions
ENSG00000232536	chromatin interactions
ENSG00000101608	chromatin interactions
ENSG00000236605	chromatin interactions
ENSG00000100983	chromatin interactions
ENSG00000252989	chromatin interactions
ENSG00000154174	chromatin interactions

Extended variants
information (count: 3996 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:3996 , 50 per page) page: 1 2 3 4 5 6 7 ... 80

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs536911439	chr3:100342316-100342317	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs574879951	chr3:100342328-100342329	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs535841715	chr3:100342336-100342337	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs191310959	chr3:100342343-100342344	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs116703933	chr3:100342378-100342379	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs9851125	chr3:100342379-100342380	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs183700999	chr3:100342387-100342388	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs77042261	chr3:100342412-100342413	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs188447195	chr3:100342418-100342419	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs572717140	chr3:100342444-100342445	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs559389658	chr3:100342451-100342452	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs115416542	chr3:100342456-100342457	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs1165259	chr3:100342493-100342494	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs149161069	chr3:100342537-100342538	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs530447432	chr3:100342560-100342561	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs182392801	chr3:100342568-100342569	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs570425561	chr3:100342569-100342570	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs373946545	chr3:100342592-100342593	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs112823994	chr3:100342595-100342596	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs148298856	chr3:100342607-100342608	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs568517137	chr3:100342617-100342618	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs535607027	chr3:100342640-100342641	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs532269234	chr3:100342642-100342643	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs112946280	chr3:100342708-100342709	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs150378081	chr3:100342720-100342721	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs549928066	chr3:100342742-100342743	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs113155522	chr3:100342789-100342790	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs187191346	chr3:100342847-100342848	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs529822478	chr3:100342856-100342857	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs190081946	chr3:100342923-100342924	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs547995096	chr3:100342959-100342960	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs373616093	chr3:100342990-100342991	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs182658753	chr3:100343829-100343830	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs544801263	chr3:100343864-100343865	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs534650668	chr3:100343938-100343939	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs556631161	chr3:100343990-100343991	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs185034768	chr3:100344055-100344056	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs114192210	chr3:100344099-100344100	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs563770895	chr3:100344103-100344104	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs144466693	chr3:100344107-100344108	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs148403645	chr3:100344112-100344113	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs562017616	chr3:100344183-100344184	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs142492448	chr3:100344203-100344204	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs550833600	chr3:100344217-100344218	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs113683881	chr3:100344238-100344239	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs1165256	chr3:100344244-100344245	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs189891777	chr3:100344273-100344274	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs183859608	chr3:100344280-100344281	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs1165255	chr3:100344331-100344332	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs145594140	chr3:100344346-100344347	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:61)

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
Ovarian clear cell carcinoma	21343371	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD

Chromatin state (count:1725 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:100339800-100343000	Weak transcription	Fetal Intestine Large	intestine
2	chr3:100343800-100352000	Weak transcription	Fetal Intestine Large	intestine
3	chr3:100346200-100348000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr3:100346400-100348200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
5	chr3:100347400-100347600	Enhancers	Small Intestine	intestine
6	chr3:100347400-100348600	Enhancers	Primary hematopoietic stem cells	blood
7	chr3:100347600-100349200	Weak transcription	Small Intestine	intestine
8	chr3:100347600-100350000	Enhancers	HUVEC	blood vessel
9	chr3:100347600-100350400	Enhancers	K562	blood
10	chr3:100347800-100349800	Enhancers	Primary hematopoietic stem cells short term culture	blood
11	chr3:100348000-100348800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr3:100348200-100348600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
13	chr3:100348200-100349800	Enhancers	NHEK	skin
14	chr3:100348200-100352200	Weak transcription	Primary neutrophils fromperipheralblood	blood
15	chr3:100348400-100349200	Enhancers	Duodenum Mucosa	Duodenum
16	chr3:100348400-100349400	Enhancers	Fetal Intestine Small	intestine
17	chr3:100348400-100350600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
18	chr3:100348400-100350600	Enhancers	HMEC	breast
19	chr3:100348600-100349800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
20	chr3:100348600-100350200	Enhancers	Hela-S3	cervix
21	chr3:100348600-100350400	Enhancers	HUES64 Cell Line	embryonic stem cell
22	chr3:100348600-100353400	Weak transcription	Primary hematopoietic stem cells	blood
23	chr3:100348600-100354200	Weak transcription	Sigmoid Colon	Sigmoid Colon
24	chr3:100348800-100349800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr3:100349000-100350400	Enhancers	iPS-15b Cell Line	embryonic stem cell
26	chr3:100349000-100350600	Enhancers	ES-I3 Cell Line	embryonic stem cell
27	chr3:100349000-100350600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
28	chr3:100349200-100349400	Enhancers	Small Intestine	intestine
29	chr3:100349200-100350200	Enhancers	A549	lung
30	chr3:100349200-100350400	Enhancers	HUES6 Cell Line	embryonic stem cell
31	chr3:100349200-100350400	Enhancers	iPS-18 Cell Line	embryonic stem cell
32	chr3:100349200-100350600	Enhancers	iPS-20b Cell Line	embryonic stem cell
33	chr3:100349200-100352400	Weak transcription	Duodenum Mucosa	Duodenum
34	chr3:100349400-100352800	Weak transcription	Fetal Intestine Small	intestine
35	chr3:100349600-100349800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr3:100349600-100349800	Bivalent Enhancer	NHDF-Ad	bronchial
37	chr3:100349600-100350400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
38	chr3:100349600-100350400	Enhancers	H9 Cell Line	embryonic stem cell
39	chr3:100349800-100350000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr3:100349800-100352600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
41	chr3:100349800-100352800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
42	chr3:100349800-100352800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
43	chr3:100350400-100353600	Weak transcription	K562	blood
44	chr3:100350600-100353600	Weak transcription	HMEC	breast
45	chr3:100350600-100354000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
46	chr3:100352000-100353000	Strong transcription	Fetal Intestine Large	intestine
47	chr3:100352200-100353800	Strong transcription	Primary neutrophils fromperipheralblood	blood
48	chr3:100352400-100353000	Strong transcription	Duodenum Mucosa	Duodenum
49	chr3:100352600-100354600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
50	chr3:100352800-100353400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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