Variant report

Variant	nsv1004273
Chromosome Location	chr3:100350244-100427937
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1089)
CpG islands
(count:368)
Chromatin interactive
region (count:48)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1089 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

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	chr3:100359648-100359874	HepG2	liver:	n/a	n/a
3	ARID3A	chr3:100353734-100354533	HepG2	liver:	n/a	n/a
4	ARID3A	chr3:100427756-100428585	HepG2	liver:	n/a	n/a
5	ARID3A	chr3:100381238-100381404	K562	blood:	n/a	n/a
6	ARID3A	chr3:100353731-100353930	K562	blood:	n/a	n/a
7	ARID3A	chr3:100400484-100400645	HepG2	liver:	n/a	n/a
8	ATF1	chr3:100353718-100353993	K562	blood:	n/a	n/a
9	ATF2	chr3:100427777-100428567	GM12878	blood:	n/a	n/a
10	ATF2	chr3:100360476-100360923	GM12878	blood:	n/a	n/a
11	ATF2	chr3:100369506-100370238	GM12878	blood:	n/a	n/a
12	ATF3	chr3:100370050-100370425	K562	blood:	n/a	n/a
13	BACH1	chr3:100421452-100421833	K562	blood:	n/a	n/a
14	BACH1	chr3:100421524-100421801	H1-hESC	embryonic stem cell:	n/a	n/a
15	BACH1	chr3:100381410-100381594	K562	blood:	n/a	n/a
16	BATF	chr3:100360218-100360885	GM12878	blood:	n/a	chr3:100360555-100360566
17	BATF	chr3:100360240-100360471	GM12878	blood:	n/a	n/a
18	BATF	chr3:100369685-100370004	GM12878	blood:	n/a	n/a
19	BATF	chr3:100369687-100370030	GM12878	blood:	n/a	n/a
20	BCL11A	chr3:100360195-100360894	GM12878	blood:	n/a	n/a
21	BCL11A	chr3:100360611-100360835	GM12878	blood:	n/a	n/a
22	BCL11A	chr3:100360235-100360494	GM12878	blood:	n/a	n/a
23	BHLHE40	chr3:100427893-100428554	GM12878	blood:	n/a	chr3:100428533-100428549
24	BHLHE40	chr3:100353728-100354019	HepG2	liver:	n/a	n/a
25	BHLHE40	chr3:100369647-100370331	GM12878	blood:	n/a	n/a
26	BHLHE40	chr3:100353702-100354034	K562	blood:	n/a	n/a
27	BHLHE40	chr3:100353686-100354022	GM12878	blood:	n/a	n/a
28	BHLHE40	chr3:100360142-100360910	GM12878	blood:	n/a	n/a
29	BRCA1	chr3:100427800-100428582	H1-hESC	embryonic stem cell:	n/a	n/a
30	BRCA1	chr3:100427676-100428558	Hela-S3	cervix:	n/a	n/a
31	BRCA1	chr3:100427866-100428531	GM12878	blood:	n/a	n/a
32	CBX3	chr3:100427818-100428510	K562	blood:	n/a	n/a
33	CBX3	chr3:100415727-100416040	K562	blood:	n/a	n/a
34	CCNT2	chr3:100427839-100429006	K562	blood:	n/a	chr3:100428771-100428780 chr3:100428796-100428805
35	CEBPB	chr3:100370681-100370966	K562	blood:	n/a	n/a
36	CEBPB	chr3:100384545-100384598	K562	blood:	n/a	chr3:100384580-100384591
37	CEBPB	chr3:100373411-100373726	HepG2	liver:	n/a	chr3:100373575-100373586
38	CEBPB	chr3:100385560-100385922	IMR90	lung:	n/a	chr3:100385738-100385749
39	CEBPB	chr3:100399324-100399534	HepG2	liver:	n/a	chr3:100399445-100399456
40	CEBPB	chr3:100421369-100421475	Hela-S3	cervix:	n/a	n/a
41	CEBPB	chr3:100399373-100399510	IMR90	lung:	n/a	chr3:100399445-100399456
42	CEBPB	chr3:100353821-100353823	Hela-S3	cervix:	n/a	n/a
43	CEBPB	chr3:100350095-100350440	Hela-S3	cervix:	n/a	n/a
44	CEBPB	chr3:100373450-100373663	K562	blood:	n/a	chr3:100373575-100373586
45	CEBPB	chr3:100400369-100400703	HepG2	liver:	n/a	n/a
46	CEBPB	chr3:100381321-100381668	Hela-S3	cervix:	n/a	n/a
47	CEBPB	chr3:100416846-100416982	HepG2	liver:	n/a	chr3:100416923-100416934
48	CEBPB	chr3:100416737-100417099	HepG2	liver:	n/a	chr3:100416923-100416934
49	CEBPB	chr3:100373432-100373699	A549	lung:	n/a	chr3:100373575-100373586
50	CEBPB	chr3:100381066-100381689	K562	blood:	n/a	n/a

(count:368 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:100401284-100401334	GM12891	blood:	n/a
2	chr3:100401284-100401334	MCF-7	breast:	n/a
3	chr3:100401284-100401334	GM12891	blood:	n/a
4	chr3:100401284-100401334	MCF-7	breast:	n/a
5	chr3:100427096-100427146	SK-N-SH_RA	brain:	n/a
6	chr3:100401270-100401320	RPTEC	kidney:	n/a
7	chr3:100401284-100401334	HCM	heart:	n/a
8	chr3:100401284-100401334	SK-N-SH_RA	brain:	n/a
9	chr3:100401200-100401250	CMK	blood:	n/a
10	chr3:100427239-100427289	BJ	skin:	n/a
11	chr3:100401284-100401334	T-47D	breast:	n/a
12	chr3:100401270-100401320	HMEC	breast:	n/a
13	chr3:100424830-100424880	HNPCEpiC	eye:	n/a
14	chr3:100401284-100401334	K562	blood:	n/a
15	chr3:100401284-100401334	BJ	skin:	n/a
16	chr3:100401270-100401320	LNCaP	prostate:	n/a
17	chr3:100424830-100424880	HUVEC	blood vessel:	n/a
18	chr3:100424830-100424880	AG04449	skin:	fetal
19	chr3:100401270-100401320	NT2-D1	testis:	n/a
20	chr3:100427239-100427289	HRPEpiC	eye:	n/a
21	chr3:100427239-100427289	HEK293	kidney:	embryo
22	chr3:100427239-100427289	GM19239	blood:	n/a
23	chr3:100401270-100401320	HAEpiC	amniotic membrane:	n/a
24	chr3:100401284-100401334	HCF	heart:	n/a
25	chr3:100424830-100424880	K562	blood:	n/a
26	chr3:100427096-100427146	Hepatocyte	liver:	n/a
27	chr3:100401200-100401250	PFSK-1	brain:	n/a
28	chr3:100424830-100424880	GM12878	blood:	n/a
29	chr3:100401200-100401250	AG04450	lung:	fetal
30	chr3:100427096-100427146	ECC-1	luminal epithelium:	n/a
31	chr3:100401284-100401334	SAEC	small airway:	n/a
32	chr3:100401200-100401250	ECC-1	luminal epithelium:	n/a
33	chr3:100427239-100427289	ovcar-3	ovarian:	n/a
34	chr3:100424830-100424880	SK-N-MC	brain:	n/a
35	chr3:100401200-100401250	SK-N-MC	brain:	n/a
36	chr3:100401270-100401320	GM06990	blood:	n/a
37	chr3:100401200-100401250	K562	blood:	n/a
38	chr3:100401270-100401320	HNPCEpiC	eye:	n/a
39	chr3:100401284-100401334	NHDF-neo	bronchial:	n/a
40	chr3:100401284-100401334	ovcar-3	ovarian:	n/a
41	chr3:100427239-100427289	HNPCEpiC	eye:	n/a
42	chr3:100427096-100427146	SKMC	muscle:	n/a
43	chr3:100401270-100401320	SK-N-SH_RA	brain:	n/a
44	chr3:100401200-100401250	HEEpiC	esophagus:	n/a
45	chr3:100401200-100401250	HCM	heart:	n/a
46	chr3:100401270-100401320	HRCEpiC	kidney:	n/a
47	chr3:100427239-100427289	HUVEC	blood vessel:	n/a
48	chr3:100427096-100427146	HCT-116	colon:	n/a
49	chr3:100427096-100427146	HUVEC	blood vessel:	n/a
50	chr3:100401270-100401320	MCF10A-Er-Src	breast:	n/a

(count:48 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:100414154..100421316-chr3:100422241..100429195,9	MCF-7	breast:
2	chr3:100325466..100327241-chr3:100349090..100350621,2	K562	blood:
3	chr3:100322114..100322780-chr3:100353316..100353989,3	MCF-7	breast:
4	chr3:100181153..100182757-chr3:100352927..100354311,7	MCF-7	breast:
5	chr3:100419538..100421699-chr3:100430283..100434420,3	MCF-7	breast:
6	chr18:3247419..3248282-chr3:100427656..100428171,2	Hela-S3	cervix:
7	chr3:100410212..100413199-chr3:100413505..100415346,2	K562	blood:
8	chr3:100353552..100356244-chr3:100358458..100360777,2	K562	blood:
9	chr3:100118924..100121912-chr3:100362623..100364573,2	K562	blood:
10	chr3:100358087..100360713-chr3:100362813..100364716,2	K562	blood:
11	chr3:100321992..100322818-chr3:100353419..100354308,2	MCF-7	breast:
12	chr3:100181696..100182432-chr3:100355242..100355805,2	MCF-7	breast:
13	chr3:100415596..100419109-chr3:100421112..100424187,4	K562	blood:
14	chr3:100412000..100414603-chr3:100428096..100429901,2	K562	blood:
15	chr3:100358087..100360713-chr3:100362813..100364716,2	K562	blood:
16	chr3:100372478..100376338-chr3:100378859..100382078,3	K562	blood:
17	chr3:100348848..100350778-chr3:100351417..100355406,3	K562	blood:
18	chr3:100420077..100423053-chr3:100428087..100429810,2	MCF-7	breast:
19	chr3:100340717..100343040-chr3:100348395..100351881,3	K562	blood:
20	chr3:100279818..100281392-chr3:100419411..100421780,2	K562	blood:
21	chr3:100367436..100369530-chr3:100426605..100429472,2	MCF-7	breast:
22	chr3:100120818..100123698-chr3:100370041..100372201,2	K562	blood:
23	chr3:100321003..100323549-chr3:100347554..100350487,3	MCF-7	breast:
24	chr20:33543190..33544135-chr3:100427443..100428252,2	NB4	blood:
25	chr3:100120411..100122999-chr3:100364924..100367578,2	K562	blood:
26	chr3:100419966..100423130-chr3:100426813..100428964,3	K562	blood:
27	chr17:57918588..57920867-chr3:100426772..100429347,2	MCF-7	breast:
28	chr3:100348848..100350394-chr3:100351417..100354134,2	K562	blood:
29	chr3:100415596..100419109-chr3:100421112..100424187,4	K562	blood:
30	chr3:100427232..100427732-chr9:96215167..96215670,2	Hela-S3	cervix:
31	chr3:100423356..100425214-chr3:100428038..100429852,2	K562	blood:
32	chr3:100325407..100326196-chr3:100353394..100354270,2	MCF-7	breast:
33	chr3:100412832..100415800-chr3:100417725..100420372,2	K562	blood:
34	chr3:100355413..100357441-chr3:100427541..100429664,2	K562	blood:
35	chr3:100369607..100371401-chr3:100374454..100376110,2	K562	blood:
36	chr3:100364940..100366707-chr3:100366782..100369483,3	K562	blood:
37	chr3:100352243..100354477-chr3:100424707..100427239,2	MCF-7	breast:
38	chr3:100348848..100350394-chr3:100351417..100354134,2	K562	blood:
39	chr3:100369607..100371401-chr3:100374454..100376110,2	K562	blood:
40	chr1:73273811..73275334-chr3:100425817..100428133,2	MCF-7	breast:
41	chr3:100325886..100329093-chr3:100426560..100431642,4	MCF-7	breast:
42	chr3:100412832..100415800-chr3:100417725..100420372,2	K562	blood:
43	chr3:100417750..100419779-chr3:100427601..100429655,2	K562	blood:
44	chr3:100374838..100376761-chr3:100378684..100380359,2	K562	blood:
45	chr3:100374838..100376761-chr3:100378684..100380359,2	K562	blood:
46	chr3:100421148..100423017-chr3:100443429..100446212,2	K562	blood:
47	chr3:100118702..100121299-chr3:100427057..100432444,4	K562	blood:
48	chr3:100410212..100413199-chr3:100413505..100415346,2	K562	blood:

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

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

No data

Variant related genes	Relation type
GPR128	TF binding region
TFG	TF binding region
ENSG00000252989	TF binding region
GMFBP1	TF binding region
GPR128	CpG island
TFG	CpG island
ENSG00000252989	CpG island
GMFBP1	CpG island
ENSG00000100983	chromatin interactions
ENSG00000188938	chromatin interactions
ENSG00000154174	chromatin interactions
ENSG00000252989	chromatin interactions
ENSG00000101608	chromatin interactions
ENSG00000144820	chromatin interactions
ENSG00000199004	chromatin interactions
ENSG00000206535	chromatin interactions
ENSG00000114354	chromatin interactions

Extended variants
information (count: 3178 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:3178 , 50 per page) page: 1 2 3 4 5 6 7 ... 64

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1144126	chr3:100350244-100350245	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs16842433	chr3:100350247-100350248	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs76854766	chr3:100350266-100350267	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs551113217	chr3:100350273-100350274	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs540323584	chr3:100350302-100350303	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs569248362	chr3:100350348-100350349	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs368046837	chr3:100350349-100350350	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs376900064	chr3:100350361-100350362	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs558997348	chr3:100350381-100350382	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs16842435	chr3:100350394-100350395	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs567194660	chr3:100350428-100350429	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs534109778	chr3:100350481-100350482	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs555960515	chr3:100350487-100350488	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs370372107	chr3:100350507-100350508	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs187235257	chr3:100350517-100350518	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs535148835	chr3:100350544-100350545	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs116792084	chr3:100350558-100350559	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs574851759	chr3:100350576-100350577	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs545820728	chr3:100350600-100350601	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs375072386	chr3:100350645-100350646	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs147152886	chr3:100350688-100350689	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs1144125	chr3:100350745-100350746	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
23	rs540040227	chr3:100350775-100350776	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs192629522	chr3:100350792-100350793	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs138665837	chr3:100350821-100350822	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs555377845	chr3:100350874-100350875	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs551049937	chr3:100350875-100350876	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs142677259	chr3:100350942-100350943	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs533165107	chr3:100350991-100350992	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs550342663	chr3:100351038-100351039	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs551780675	chr3:100351041-100351042	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs567037290	chr3:100351053-100351054	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs534470186	chr3:100351171-100351172	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs549287537	chr3:100351197-100351198	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs567471675	chr3:100351217-100351218	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs538057754	chr3:100351278-100351279	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs563165578	chr3:100351336-100351337	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs184244712	chr3:100351342-100351343	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs556625321	chr3:100351359-100351360	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs575039993	chr3:100351395-100351396	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs572722272	chr3:100351462-100351463	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs557772174	chr3:100351468-100351469	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs572767558	chr3:100351497-100351498	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs16842436	chr3:100351506-100351507	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs147330891	chr3:100351512-100351513	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs116606932	chr3:100351522-100351523	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs566712881	chr3:100351589-100351590	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs562967697	chr3:100351665-100351666	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs1145350	chr3:100351696-100351697	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs188010074	chr3:100351785-100351786	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:685 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:100343800-100352000	Weak transcription	Fetal Intestine Large	intestine
2	chr3:100347600-100350400	Enhancers	K562	blood
3	chr3:100348200-100352200	Weak transcription	Primary neutrophils fromperipheralblood	blood
4	chr3:100348400-100350600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr3:100348400-100350600	Enhancers	HMEC	breast
6	chr3:100348600-100350400	Enhancers	HUES64 Cell Line	embryonic stem cell
7	chr3:100348600-100353400	Weak transcription	Primary hematopoietic stem cells	blood
8	chr3:100348600-100354200	Weak transcription	Sigmoid Colon	Sigmoid Colon
9	chr3:100349000-100350400	Enhancers	iPS-15b Cell Line	embryonic stem cell
10	chr3:100349000-100350600	Enhancers	ES-I3 Cell Line	embryonic stem cell
11	chr3:100349000-100350600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
12	chr3:100349200-100350400	Enhancers	HUES6 Cell Line	embryonic stem cell
13	chr3:100349200-100350400	Enhancers	iPS-18 Cell Line	embryonic stem cell
14	chr3:100349200-100350600	Enhancers	iPS-20b Cell Line	embryonic stem cell
15	chr3:100349200-100352400	Weak transcription	Duodenum Mucosa	Duodenum
16	chr3:100349400-100352800	Weak transcription	Fetal Intestine Small	intestine
17	chr3:100349600-100350400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
18	chr3:100349600-100350400	Enhancers	H9 Cell Line	embryonic stem cell
19	chr3:100349800-100352600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
20	chr3:100349800-100352800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
21	chr3:100349800-100352800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
22	chr3:100350400-100353600	Weak transcription	K562	blood
23	chr3:100350600-100353600	Weak transcription	HMEC	breast
24	chr3:100350600-100354000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
25	chr3:100352000-100353000	Strong transcription	Fetal Intestine Large	intestine
26	chr3:100352200-100353800	Strong transcription	Primary neutrophils fromperipheralblood	blood
27	chr3:100352400-100353000	Strong transcription	Duodenum Mucosa	Duodenum
28	chr3:100352600-100354600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
29	chr3:100352800-100353400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chr3:100352800-100354000	Enhancers	Primary hematopoietic stem cells short term culture	blood
31	chr3:100352800-100354800	Enhancers	Fetal Intestine Small	intestine
32	chr3:100353000-100353800	Enhancers	Liver	Liver
33	chr3:100353000-100353800	Enhancers	Duodenum Mucosa	Duodenum
34	chr3:100353000-100353800	Genic enhancers	Fetal Intestine Large	intestine
35	chr3:100353200-100354000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
36	chr3:100353400-100353600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
37	chr3:100353400-100353800	Enhancers	Rectal Mucosa Donor 29	rectum
38	chr3:100353400-100354000	Enhancers	Breast Myoepithelial Primary Cells	Breast
39	chr3:100353400-100354000	Enhancers	Primary hematopoietic stem cells	blood
40	chr3:100353400-100354000	Enhancers	HSMMtube	muscle
41	chr3:100353400-100354400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
42	chr3:100353400-100354600	Enhancers	Stomach Mucosa	stomach
43	chr3:100353600-100353800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
44	chr3:100353600-100353800	Enhancers	HepG2	liver
45	chr3:100353600-100354000	Enhancers	Fetal Brain Male	brain
46	chr3:100353600-100354400	Enhancers	Rectal Mucosa Donor 31	rectum
47	chr3:100353600-100354400	Enhancers	HMEC	breast
48	chr3:100353600-100354400	Enhancers	K562	blood
49	chr3:100353800-100354000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
50	chr3:100353800-100354000	Flanking Active TSS	Duodenum Mucosa	Duodenum

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