Variant report

Variant	nsv460775
Chromosome Location	chr3:100350745-100433592
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1622)
CpG islands
(count:1100)
Chromatin interactive
region (count:56)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1622 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:100400484-100400645	HepG2	liver:	n/a	n/a
2	ARID3A	chr3:100353734-100354533	HepG2	liver:	n/a	n/a
3	ARID3A	chr3:100381238-100381404	K562	blood:	n/a	n/a
4	ARID3A	chr3:100359648-100359874	HepG2	liver:	n/a	n/a
5	ARID3A	chr3:100428405-100428550	K562	blood:	n/a	n/a
6	ARID3A	chr3:100427756-100428585	HepG2	liver:	n/a	n/a
7	ARID3A	chr3:100369723-100370159	K562	blood:	n/a	n/a
8	ARID3A	chr3:100353731-100353930	K562	blood:	n/a	n/a
9	ATF1	chr3:100427978-100428440	K562	blood:	n/a	n/a
10	ATF1	chr3:100353718-100353993	K562	blood:	n/a	n/a
11	ATF2	chr3:100429275-100429952	GM12878	blood:	n/a	n/a
12	ATF2	chr3:100427777-100428567	GM12878	blood:	n/a	n/a
13	ATF2	chr3:100360476-100360923	GM12878	blood:	n/a	n/a
14	ATF2	chr3:100369506-100370238	GM12878	blood:	n/a	n/a
15	ATF3	chr3:100370050-100370425	K562	blood:	n/a	n/a
16	BACH1	chr3:100381410-100381594	K562	blood:	n/a	n/a
17	BACH1	chr3:100421524-100421801	H1-hESC	embryonic stem cell:	n/a	n/a
18	BACH1	chr3:100421452-100421833	K562	blood:	n/a	n/a
19	BACH1	chr3:100428023-100428678	H1-hESC	embryonic stem cell:	n/a	n/a
20	BATF	chr3:100360218-100360885	GM12878	blood:	n/a	chr3:100360555-100360566
21	BATF	chr3:100369687-100370030	GM12878	blood:	n/a	n/a
22	BATF	chr3:100369685-100370004	GM12878	blood:	n/a	n/a
23	BATF	chr3:100429220-100429801	GM12878	blood:	n/a	n/a
24	BATF	chr3:100429333-100429812	GM12878	blood:	n/a	n/a
25	BATF	chr3:100360240-100360471	GM12878	blood:	n/a	n/a
26	BCL11A	chr3:100360611-100360835	GM12878	blood:	n/a	n/a
27	BCL11A	chr3:100360235-100360494	GM12878	blood:	n/a	n/a
28	BCL11A	chr3:100360195-100360894	GM12878	blood:	n/a	n/a
29	BCLAF1	chr3:100429350-100429879	GM12878	blood:	n/a	chr3:100429694-100429703 chr3:100429744-100429753 chr3:100429743-100429752
30	BCLAF1	chr3:100428169-100428667	GM12878	blood:	n/a	chr3:100428545-100428558 chr3:100428541-100428554 chr3:100428539-100428552
31	BHLHE40	chr3:100427985-100428525	K562	blood:	n/a	n/a
32	BHLHE40	chr3:100428011-100428266	A549	lung:	n/a	n/a
33	BHLHE40	chr3:100428885-100428960	K562	blood:	n/a	n/a
34	BHLHE40	chr3:100369647-100370331	GM12878	blood:	n/a	n/a
35	BHLHE40	chr3:100353702-100354034	K562	blood:	n/a	n/a
36	BHLHE40	chr3:100360142-100360910	GM12878	blood:	n/a	n/a
37	BHLHE40	chr3:100427970-100428628	HepG2	liver:	n/a	chr3:100428533-100428549
38	BHLHE40	chr3:100353686-100354022	GM12878	blood:	n/a	n/a
39	BHLHE40	chr3:100427893-100428554	GM12878	blood:	n/a	chr3:100428533-100428549
40	BHLHE40	chr3:100353728-100354019	HepG2	liver:	n/a	n/a
41	BRCA1	chr3:100429415-100429752	Hela-S3	cervix:	n/a	n/a
42	BRCA1	chr3:100428290-100428586	HepG2	liver:	n/a	n/a
43	BRCA1	chr3:100427800-100428582	H1-hESC	embryonic stem cell:	n/a	n/a
44	BRCA1	chr3:100428898-100429175	H1-hESC	embryonic stem cell:	n/a	n/a
45	BRCA1	chr3:100427866-100428531	GM12878	blood:	n/a	n/a
46	BRCA1	chr3:100427676-100428558	Hela-S3	cervix:	n/a	n/a
47	CBX3	chr3:100415727-100416040	K562	blood:	n/a	n/a
48	CBX3	chr3:100429573-100429981	K562	blood:	n/a	n/a
49	CBX3	chr3:100427818-100428510	K562	blood:	n/a	n/a
50	CCNT2	chr3:100427839-100429006	K562	blood:	n/a	chr3:100428771-100428780 chr3:100428796-100428805

(count:1100 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:100428005-100428055	HL-60	blood:	n/a
2	chr3:100424830-100424880	HEEpiC	esophagus:	n/a
3	chr3:100428005-100428055	HL-60	blood:	n/a
4	chr3:100424830-100424880	HEEpiC	esophagus:	n/a
5	chr3:100429064-100429114	AG04450	lung:	fetal
6	chr3:100428145-100428195	AoSMC	blood vessel:	n/a
7	chr3:100428147-100428197	GM19239	blood:	n/a
8	chr3:100401270-100401320	MCF-7	breast:	n/a
9	chr3:100430811-100430861	H1-hESC	embryonic stem cell:	embryo
10	chr3:100428145-100428195	HRCEpiC	kidney:	n/a
11	chr3:100424830-100424880	HL-60	blood:	n/a
12	chr3:100430811-100430861	NT2-D1	testis:	n/a
13	chr3:100401200-100401250	AG10803	skin:	n/a
14	chr3:100424830-100424880	HCM	heart:	n/a
15	chr3:100428070-100428120	T-47D	breast:	n/a
16	chr3:100401270-100401320	HCT-116	colon:	n/a
17	chr3:100428070-100428120	PANC-1	pancreas:	n/a
18	chr3:100401270-100401320	HRE	kidney:	n/a
19	chr3:100429064-100429114	GM19239	blood:	n/a
20	chr3:100428869-100428919	AG09309	skin:	n/a
21	chr3:100401200-100401250	HNPCEpiC	eye:	n/a
22	chr3:100427096-100427146	PFSK-1	brain:	n/a
23	chr3:100401200-100401250	GM19239	blood:	n/a
24	chr3:100401284-100401334	PFSK-1	brain:	n/a
25	chr3:100428033-100428083	AoSMC	blood vessel:	n/a
26	chr3:100427096-100427146	HepG2	liver:	n/a
27	chr3:100428147-100428197	T-47D	breast:	n/a
28	chr3:100401270-100401320	AG09319	gingival:	n/a
29	chr3:100430811-100430861	A549	lung:	n/a
30	chr3:100427239-100427289	NB4	blood:	n/a
31	chr3:100428869-100428919	NHBE	bronchial:	n/a
32	chr3:100428147-100428197	AG04449	skin:	fetal
33	chr3:100428147-100428197	IMR90	lung:	fetal
34	chr3:100428145-100428195	ProgFib	skin:	n/a
35	chr3:100427096-100427146	NH-A	brain:	n/a
36	chr3:100428642-100428692	Jurkat	blood:	n/a
37	chr3:100424830-100424880	GM12892	blood:	n/a
38	chr3:100428005-100428055	Hepatocyte	liver:	n/a
39	chr3:100428147-100428197	AG09319	gingival:	n/a
40	chr3:100428145-100428195	HMEC	breast:	n/a
41	chr3:100428642-100428692	HRCEpiC	kidney:	n/a
42	chr3:100427239-100427289	SK-N-SH	brain:	n/a
43	chr3:100401284-100401334	AG09319	gingival:	n/a
44	chr3:100427096-100427146	ProgFib	skin:	n/a
45	chr3:100401270-100401320	ovcar-3	ovarian:	n/a
46	chr3:100428869-100428919	SKMC	muscle:	n/a
47	chr3:100428147-100428197	NHBE	bronchial:	n/a
48	chr3:100428398-100428448	AG09309	skin:	n/a
49	chr3:100428172-100428222	MCF-7	breast:	n/a
50	chr3:100428005-100428055	HCM	heart:	n/a

(count:56 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr3:100428105..100429880-chr3:100429992..100431694,2	K562	blood:
2	chr3:100353552..100356244-chr3:100358458..100360777,2	K562	blood:
3	chr3:100414154..100421316-chr3:100422241..100429195,9	MCF-7	breast:
4	chr3:100432846..100436544-chr3:100436912..100439975,5	K562	blood:
5	chr3:100432153..100434876-chr3:100437236..100438974,2	MCF-7	breast:
6	chr3:100419538..100421699-chr3:100430283..100434420,3	MCF-7	breast:
7	chr3:100412000..100414603-chr3:100428096..100429901,2	K562	blood:
8	chr3:100369607..100371401-chr3:100374454..100376110,2	K562	blood:
9	chr17:57918588..57920867-chr3:100426772..100429347,2	MCF-7	breast:
10	chr3:100415596..100419109-chr3:100421112..100424187,4	K562	blood:
11	chr3:100120818..100123698-chr3:100370041..100372201,2	K562	blood:
12	chr3:100369607..100371401-chr3:100374454..100376110,2	K562	blood:
13	chr3:100181696..100182432-chr3:100355242..100355805,2	MCF-7	breast:
14	chr3:100421148..100423017-chr3:100443429..100446212,2	K562	blood:
15	chr3:100364940..100366707-chr3:100366782..100369483,3	K562	blood:
16	chr12:56435446..56435990-chr3:100428103..100428866,2	Hela-S3	cervix:
17	chr3:100340717..100343040-chr3:100348395..100351881,3	K562	blood:
18	chr3:100415596..100419109-chr3:100421112..100424187,4	K562	blood:
19	chr3:100363955..100366251-chr3:100430276..100432024,2	K562	blood:
20	chr3:100412832..100415800-chr3:100417725..100420372,2	K562	blood:
21	chr3:100427232..100427732-chr9:96215167..96215670,2	Hela-S3	cervix:
22	chr3:100420077..100423053-chr3:100428087..100429810,2	MCF-7	breast:
23	chr3:100352243..100354477-chr3:100424707..100427239,2	MCF-7	breast:
24	chr3:100325886..100329093-chr3:100426560..100431642,4	MCF-7	breast:
25	chr3:100372478..100376338-chr3:100378859..100382078,3	K562	blood:
26	chr3:100348848..100350778-chr3:100351417..100355406,3	K562	blood:
27	chr3:100428095..100432338-chr3:100432996..100435628,5	K562	blood:
28	chr3:100321992..100322818-chr3:100353419..100354308,2	MCF-7	breast:
29	chr3:100410212..100413199-chr3:100413505..100415346,2	K562	blood:
30	chr1:151512640..151513443-chr3:100428519..100429048,2	Hela-S3	cervix:
31	chr2:67550820..67551820-chr3:100427957..100428561,3	HCT-116	colon:
32	chr3:100423356..100425214-chr3:100428038..100429852,2	K562	blood:
33	chr3:100120411..100122999-chr3:100364924..100367578,2	K562	blood:
34	chr3:100367436..100369530-chr3:100426605..100429472,2	MCF-7	breast:
35	chr3:100374838..100376761-chr3:100378684..100380359,2	K562	blood:
36	chr3:100118702..100121299-chr3:100427057..100432444,4	K562	blood:
37	chr3:100412832..100415800-chr3:100417725..100420372,2	K562	blood:
38	chr3:100322114..100322780-chr3:100353316..100353989,3	MCF-7	breast:
39	chr3:100358087..100360713-chr3:100362813..100364716,2	K562	blood:
40	chr3:100355413..100357441-chr3:100427541..100429664,2	K562	blood:
41	chr3:100419538..100421699-chr3:100430283..100434420,3	MCF-7	breast:
42	chr3:100417750..100419779-chr3:100427601..100429655,2	K562	blood:
43	chr3:100325407..100326196-chr3:100353394..100354270,2	MCF-7	breast:
44	chr3:100419966..100423130-chr3:100426813..100428964,3	K562	blood:
45	chr3:100181153..100182757-chr3:100352927..100354311,7	MCF-7	breast:
46	chr3:100279818..100281392-chr3:100419411..100421780,2	K562	blood:
47	chr11:59436077..59436715-chr3:100428082..100428818,2	Hela-S3	cervix:
48	chr3:100410212..100413199-chr3:100413505..100415346,2	K562	blood:
49	chr3:100425991..100429784-chr3:100429994..100431694,4	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-ABI3BP-1	chr3:100383894-100384320	NONHSAT090876
2	lnc-TMEM45A-1	chr3:100356146-100356419	NONHSAT090874
3	lnc-TMEM45A-1	chr3:100354384-100354670	NONHSAT090874

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
ENSG00000101608	chromatin interactions
ENSG00000166889	chromatin interactions
ENSG00000206535	chromatin interactions
ENSG00000252989	chromatin interactions
ENSG00000232536	chromatin interactions
ENSG00000154174	chromatin interactions
ENSG00000188938	chromatin interactions
ENSG00000100983	chromatin interactions
ENSG00000257449	chromatin interactions
ENSG00000143367	chromatin interactions
ENSG00000144820	chromatin interactions
ENSG00000199004	chromatin interactions
ENSG00000236605	chromatin interactions
ENSG00000114354	chromatin interactions
ENSG00000197728	chromatin interactions

Extended variants
information (count: 3381 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:3381 , 50 per page) page: 1 2 3 4 5 6 7 ... 68

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1144125	chr3:100350745-100350746	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs540040227	chr3:100350775-100350776	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs192629522	chr3:100350792-100350793	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs138665837	chr3:100350821-100350822	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs555377845	chr3:100350874-100350875	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs551049937	chr3:100350875-100350876	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs142677259	chr3:100350942-100350943	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs533165107	chr3:100350991-100350992	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs550342663	chr3:100351038-100351039	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs551780675	chr3:100351041-100351042	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs567037290	chr3:100351053-100351054	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs534470186	chr3:100351171-100351172	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs549287537	chr3:100351197-100351198	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs567471675	chr3:100351217-100351218	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs538057754	chr3:100351278-100351279	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs563165578	chr3:100351336-100351337	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs184244712	chr3:100351342-100351343	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs556625321	chr3:100351359-100351360	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs575039993	chr3:100351395-100351396	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs572722272	chr3:100351462-100351463	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs557772174	chr3:100351468-100351469	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs572767558	chr3:100351497-100351498	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs16842436	chr3:100351506-100351507	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs147330891	chr3:100351512-100351513	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs116606932	chr3:100351522-100351523	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs566712881	chr3:100351589-100351590	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs562967697	chr3:100351665-100351666	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs1145350	chr3:100351696-100351697	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs188010074	chr3:100351785-100351786	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs79773218	chr3:100351812-100351813	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs549044348	chr3:100351823-100351824	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs193087349	chr3:100351837-100351838	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs4552397	chr3:100351873-100351874	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs694612	chr3:100351896-100351897	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs531782420	chr3:100351940-100351941	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs73145104	chr3:100351941-100351942	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs199760799	chr3:100352021-100352022	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs610854	chr3:100352043-100352044	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs200895145	chr3:100352109-100352110	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs114672200	chr3:100352110-100352111	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs369393091	chr3:100352129-100352130	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs143646459	chr3:100352130-100352131	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs116327172	chr3:100352151-100352152	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs138834427	chr3:100352181-100352182	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs566418219	chr3:100352183-100352184	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs533780478	chr3:100352193-100352194	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs139753956	chr3:100352223-100352224	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs373484932	chr3:100352231-100352232	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs184858793	chr3:100352233-100352234	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs377440433	chr3:100352239-100352240	Weak transcription Strong transcription	TF binding region	1 gene(s)	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:1239 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:100343800-100352000	Weak transcription	Fetal Intestine Large	intestine
2	chr3:100348200-100352200	Weak transcription	Primary neutrophils fromperipheralblood	blood
3	chr3:100348600-100353400	Weak transcription	Primary hematopoietic stem cells	blood
4	chr3:100348600-100354200	Weak transcription	Sigmoid Colon	Sigmoid Colon
5	chr3:100349200-100352400	Weak transcription	Duodenum Mucosa	Duodenum
6	chr3:100349400-100352800	Weak transcription	Fetal Intestine Small	intestine
7	chr3:100349800-100352600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr3:100349800-100352800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
9	chr3:100349800-100352800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chr3:100350400-100353600	Weak transcription	K562	blood
11	chr3:100350600-100353600	Weak transcription	HMEC	breast
12	chr3:100350600-100354000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr3:100352000-100353000	Strong transcription	Fetal Intestine Large	intestine
14	chr3:100352200-100353800	Strong transcription	Primary neutrophils fromperipheralblood	blood
15	chr3:100352400-100353000	Strong transcription	Duodenum Mucosa	Duodenum
16	chr3:100352600-100354600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
17	chr3:100352800-100353400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
18	chr3:100352800-100354000	Enhancers	Primary hematopoietic stem cells short term culture	blood
19	chr3:100352800-100354800	Enhancers	Fetal Intestine Small	intestine
20	chr3:100353000-100353800	Enhancers	Liver	Liver
21	chr3:100353000-100353800	Enhancers	Duodenum Mucosa	Duodenum
22	chr3:100353000-100353800	Genic enhancers	Fetal Intestine Large	intestine
23	chr3:100353200-100354000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
24	chr3:100353400-100353600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr3:100353400-100353800	Enhancers	Rectal Mucosa Donor 29	rectum
26	chr3:100353400-100354000	Enhancers	Breast Myoepithelial Primary Cells	Breast
27	chr3:100353400-100354000	Enhancers	Primary hematopoietic stem cells	blood
28	chr3:100353400-100354000	Enhancers	HSMMtube	muscle
29	chr3:100353400-100354400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
30	chr3:100353400-100354600	Enhancers	Stomach Mucosa	stomach
31	chr3:100353600-100353800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
32	chr3:100353600-100353800	Enhancers	HepG2	liver
33	chr3:100353600-100354000	Enhancers	Fetal Brain Male	brain
34	chr3:100353600-100354400	Enhancers	Rectal Mucosa Donor 31	rectum
35	chr3:100353600-100354400	Enhancers	HMEC	breast
36	chr3:100353600-100354400	Enhancers	K562	blood
37	chr3:100353800-100354000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
38	chr3:100353800-100354000	Flanking Active TSS	Duodenum Mucosa	Duodenum
39	chr3:100353800-100354400	Enhancers	Pancreas	Pancrea
40	chr3:100353800-100354400	Active TSS	Rectal Mucosa Donor 29	rectum
41	chr3:100353800-100354400	Flanking Active TSS	HepG2	liver
42	chr3:100353800-100354600	Active TSS	Liver	Liver
43	chr3:100353800-100355200	Weak transcription	Primary neutrophils fromperipheralblood	blood
44	chr3:100353800-100356200	Enhancers	Fetal Intestine Large	intestine
45	chr3:100354000-100354200	Enhancers	Duodenum Mucosa	Duodenum
46	chr3:100354000-100354400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
47	chr3:100354000-100354600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
48	chr3:100354000-100357800	Weak transcription	Fetal Brain Male	brain
49	chr3:100354200-100354400	Enhancers	Sigmoid Colon	Sigmoid Colon
50	chr3:100354200-100354600	Flanking Active TSS	Duodenum Mucosa	Duodenum

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