Variant report

Variant	nsv591159
Chromosome Location	chr3:100346146-100444854
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1749)
CpG islands
(count:1221)
Chromatin interactive
region (count:75)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1749 , 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	chr3:100428405-100428550	K562	blood:	n/a	n/a
2	ARID3A	chr3:100353734-100354533	HepG2	liver:	n/a	n/a
3	ARID3A	chr3:100348388-100349223	K562	blood:	n/a	n/a
4	ARID3A	chr3:100359648-100359874	HepG2	liver:	n/a	n/a
5	ARID3A	chr3:100381238-100381404	K562	blood:	n/a	n/a
6	ARID3A	chr3:100369723-100370159	K562	blood:	n/a	n/a
7	ARID3A	chr3:100400484-100400645	HepG2	liver:	n/a	n/a
8	ARID3A	chr3:100353731-100353930	K562	blood:	n/a	n/a
9	ARID3A	chr3:100427756-100428585	HepG2	liver:	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	chr3:100429275-100429952	GM12878	blood:	n/a	n/a
15	ATF2	chr3:100369506-100370238	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	chr3:100428023-100428678	H1-hESC	embryonic stem cell:	n/a	n/a
21	BACH1	chr3:100421452-100421833	K562	blood:	n/a	n/a
22	BACH1	chr3:100421524-100421801	H1-hESC	embryonic stem cell:	n/a	n/a
23	BACH1	chr3:100381410-100381594	K562	blood:	n/a	n/a
24	BATF	chr3:100360218-100360885	GM12878	blood:	n/a	chr3:100360555-100360566
25	BATF	chr3:100429220-100429801	GM12878	blood:	n/a	n/a
26	BATF	chr3:100429333-100429812	GM12878	blood:	n/a	n/a
27	BATF	chr3:100369685-100370004	GM12878	blood:	n/a	n/a
28	BATF	chr3:100369687-100370030	GM12878	blood:	n/a	n/a
29	BATF	chr3:100360240-100360471	GM12878	blood:	n/a	n/a
30	BCL11A	chr3:100360611-100360835	GM12878	blood:	n/a	n/a
31	BCL11A	chr3:100360195-100360894	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	chr3:100427893-100428554	GM12878	blood:	n/a	chr3:100428533-100428549
36	BHLHE40	chr3:100428885-100428960	K562	blood:	n/a	n/a
37	BHLHE40	chr3:100427970-100428628	HepG2	liver:	n/a	chr3:100428533-100428549
38	BHLHE40	chr3:100428011-100428266	A549	lung:	n/a	n/a
39	BHLHE40	chr3:100353728-100354019	HepG2	liver:	n/a	n/a
40	BHLHE40	chr3:100360142-100360910	GM12878	blood:	n/a	n/a
41	BHLHE40	chr3:100353686-100354022	GM12878	blood:	n/a	n/a
42	BHLHE40	chr3:100427985-100428525	K562	blood:	n/a	n/a
43	BHLHE40	chr3:100353702-100354034	K562	blood:	n/a	n/a
44	BHLHE40	chr3:100369647-100370331	GM12878	blood:	n/a	n/a
45	BRCA1	chr3:100427676-100428558	Hela-S3	cervix:	n/a	n/a
46	BRCA1	chr3:100428290-100428586	HepG2	liver:	n/a	n/a
47	BRCA1	chr3:100429415-100429752	Hela-S3	cervix:	n/a	n/a
48	BRCA1	chr3:100427866-100428531	GM12878	blood:	n/a	n/a
49	BRCA1	chr3:100428898-100429175	H1-hESC	embryonic stem cell:	n/a	n/a
50	BRCA1	chr3:100427800-100428582	H1-hESC	embryonic stem cell:	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	chr3:100401200-100401250	SK-N-MC	brain:	n/a
2	chr3:100401200-100401250	SK-N-MC	brain:	n/a
3	chr3:100429064-100429114	HCPEpiC	choroid plexus:	n/a
4	chr3:100401284-100401334	H1-hESC	embryonic stem cell:	embryo
5	chr3:100427096-100427146	HEEpiC	esophagus:	n/a
6	chr3:100401284-100401334	NHBE	bronchial:	n/a
7	chr3:100428005-100428055	U87	brain:	n/a
8	chr3:100424830-100424880	HAEpiC	amniotic membrane:	n/a
9	chr3:100428145-100428195	Hepatocyte	liver:	n/a
10	chr3:100401200-100401250	IMR90	lung:	fetal
11	chr3:100428140-100428190	SK-N-SH_RA	brain:	n/a
12	chr3:100424830-100424880	AG10803	skin:	n/a
13	chr3:100427096-100427146	U87	brain:	n/a
14	chr3:100428145-100428195	MCF10A-Er-Src	breast:	n/a
15	chr3:100424830-100424880	HRE	kidney:	n/a
16	chr3:100430811-100430861	AG10803	skin:	n/a
17	chr3:100427096-100427146	AG04450	lung:	fetal
18	chr3:100430811-100430861	AG09319	gingival:	n/a
19	chr3:100349374-100349424	HPAEpiC	pulmonary alveolar:	n/a
20	chr3:100401270-100401320	HAEpiC	amniotic membrane:	n/a
21	chr3:100401270-100401320	AG09309	skin:	n/a
22	chr3:100437347-100437397	SKMC	muscle:	n/a
23	chr3:100428005-100428055	HepG2	liver:	n/a
24	chr3:100428642-100428692	HCM	heart:	n/a
25	chr3:100428398-100428448	AG04450	lung:	fetal
26	chr3:100349374-100349424	ProgFib	skin:	n/a
27	chr3:100428398-100428448	H1-hESC	embryonic stem cell:	embryo
28	chr3:100428033-100428083	IMR90	lung:	fetal
29	chr3:100349374-100349424	Hepatocyte	liver:	n/a
30	chr3:100427239-100427289	NT2-D1	testis:	n/a
31	chr3:100437347-100437397	HPAEpiC	pulmonary alveolar:	n/a
32	chr3:100428172-100428222	Hepatocyte	liver:	n/a
33	chr3:100401200-100401250	HL-60	blood:	n/a
34	chr3:100428869-100428919	HepG2	liver:	n/a
35	chr3:100427239-100427289	Hela-S3	cervix:	n/a
36	chr3:100428070-100428120	HRCEpiC	kidney:	n/a
37	chr3:100428033-100428083	HRE	kidney:	n/a
38	chr3:100430811-100430861	HL-60	blood:	n/a
39	chr3:100424830-100424880	NHBE	bronchial:	n/a
40	chr3:100401200-100401250	HepG2	liver:	n/a
41	chr3:100349374-100349424	SK-N-SH_RA	brain:	n/a
42	chr3:100428005-100428055	BJ	skin:	n/a
43	chr3:100428398-100428448	HAEpiC	amniotic membrane:	n/a
44	chr3:100424830-100424880	Hepatocyte	liver:	n/a
45	chr3:100428642-100428692	PrEC	prostate:	n/a
46	chr3:100429064-100429114	AG10803	skin:	n/a
47	chr3:100428140-100428190	Hela-S3	cervix:	n/a
48	chr3:100427096-100427146	AoSMC	blood vessel:	n/a
49	chr3:100428147-100428197	HCPEpiC	choroid plexus:	n/a
50	chr3:100428147-100428197	GM12878	blood:	n/a

(count:75 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr3:100421148..100423017-chr3:100443429..100446212,2	K562	blood:
2	chr3:100444141..100445657-chr3:100447158..100448973,2	K562	blood:
3	chr3:100410212..100413199-chr3:100413505..100415346,2	K562	blood:
4	chr3:100412832..100415800-chr3:100417725..100420372,2	K562	blood:
5	chr3:100279818..100281392-chr3:100419411..100421780,2	K562	blood:
6	chr3:100428095..100432338-chr3:100432996..100435628,5	K562	blood:
7	chr3:100181153..100182757-chr3:100352927..100354311,7	MCF-7	breast:
8	chr3:100434706..100436343-chr3:100445572..100447869,2	K562	blood:
9	chr3:100369607..100371401-chr3:100374454..100376110,2	K562	blood:
10	chr3:100322114..100322780-chr3:100353316..100353989,3	MCF-7	breast:
11	chr3:100348848..100350394-chr3:100351417..100354134,2	K562	blood:
12	chr3:100420077..100423053-chr3:100428087..100429810,2	MCF-7	breast:
13	chr3:100353552..100356244-chr3:100358458..100360777,2	K562	blood:
14	chr3:100348848..100350394-chr3:100351417..100354134,2	K562	blood:
15	chr3:100437193..100438903-chr3:100441910..100444444,2	K562	blood:
16	chr3:100423356..100425214-chr3:100428038..100429852,2	K562	blood:
17	chr3:100118702..100121299-chr3:100427057..100432444,4	K562	blood:
18	chr3:100442764..100445441-chr3:100450170..100452232,2	K562	blood:
19	chr3:100414154..100421316-chr3:100422241..100429195,9	MCF-7	breast:
20	chr3:99535346..99537040-chr3:100436340..100438429,2	K562	blood:
21	chr3:100358087..100360713-chr3:100362813..100364716,2	K562	blood:
22	chr3:100374838..100376761-chr3:100378684..100380359,2	K562	blood:
23	chr3:100325466..100327241-chr3:100349090..100350621,2	K562	blood:
24	chr3:100432153..100434876-chr3:100437236..100438974,2	MCF-7	breast:
25	chr17:57918588..57920867-chr3:100426772..100429347,2	MCF-7	breast:
26	chr3:100437193..100438903-chr3:100441910..100444444,2	K562	blood:
27	chr3:100181696..100182432-chr3:100355242..100355805,2	MCF-7	breast:
28	chr3:100427373..100432741-chr3:100444559..100449440,6	MCF-7	breast:
29	chr3:100441058..100442704-chr3:100448594..100450149,2	K562	blood:
30	chr3:100325886..100329093-chr3:100426560..100431642,4	MCF-7	breast:
31	chr3:100410212..100413199-chr3:100413505..100415346,2	K562	blood:
32	chr11:59436077..59436715-chr3:100428082..100428818,2	Hela-S3	cervix:
33	chr3:100412832..100415800-chr3:100417725..100420372,2	K562	blood:
34	chr12:56435446..56435990-chr3:100428103..100428866,2	Hela-S3	cervix:
35	chr3:100432846..100436544-chr3:100436912..100439975,5	K562	blood:
36	chr3:100355413..100357441-chr3:100427541..100429664,2	K562	blood:
37	chr3:100415596..100419109-chr3:100421112..100424187,4	K562	blood:
38	chr3:100428339..100431099-chr3:100444238..100445960,2	MCF-7	breast:
39	chr1:73273811..73275334-chr3:100425817..100428133,2	MCF-7	breast:
40	chr3:100417750..100419779-chr3:100427601..100429655,2	K562	blood:
41	chr3:100412000..100414603-chr3:100428096..100429901,2	K562	blood:
42	chr3:100419538..100421699-chr3:100430283..100434420,3	MCF-7	breast:
43	chr3:100367436..100369530-chr3:100426605..100429472,2	MCF-7	breast:
44	chr3:100120818..100123698-chr3:100370041..100372201,2	K562	blood:
45	chr3:100427232..100427732-chr9:96215167..96215670,2	Hela-S3	cervix:
46	chr3:100432153..100434876-chr3:100437236..100438974,2	MCF-7	breast:
47	chr3:100374838..100376761-chr3:100378684..100380359,2	K562	blood:
48	chr3:100321003..100323549-chr3:100347554..100350487,3	MCF-7	breast:
49	chr3:100321992..100322818-chr3:100353419..100354308,2	MCF-7	breast:
50	chr2:67550820..67551820-chr3:100427957..100428561,3	HCT-116	colon:

(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
ENSG00000100983	chromatin interactions
ENSG00000143367	chromatin interactions
ENSG00000257449	chromatin interactions
ENSG00000197728	chromatin interactions
ENSG00000101608	chromatin interactions
ENSG00000199004	chromatin interactions
ENSG00000188938	chromatin interactions
ENSG00000232536	chromatin interactions
ENSG00000154174	chromatin interactions
ENSG00000206535	chromatin interactions
ENSG00000114354	chromatin interactions
ENSG00000236605	chromatin interactions
ENSG00000252989	chromatin interactions
ENSG00000184220	chromatin interactions
ENSG00000144820	chromatin interactions
ENSG00000166889	chromatin interactions

Extended variants
information (count: 3990 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:3990 , 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	rs190483813	chr3:100346153-100346154	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs182504521	chr3:100346158-100346159	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs629967	chr3:100346247-100346248	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs185814842	chr3:100346322-100346323	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs543077296	chr3:100346334-100346335	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs569428467	chr3:100346346-100346347	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs561226567	chr3:100346361-100346362	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs138664702	chr3:100346388-100346389	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs141232715	chr3:100346401-100346402	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs629091	chr3:100346412-100346413	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs573015201	chr3:100346443-100346444	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs532693940	chr3:100346497-100346498	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs189087674	chr3:100346504-100346505	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs566229838	chr3:100346515-100346516	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs150747605	chr3:100346599-100346600	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs140119739	chr3:100346605-100346606	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs137968026	chr3:100346634-100346635	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs115566786	chr3:100346657-100346658	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs149465263	chr3:100346735-100346736	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs181182840	chr3:100346736-100346737	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs571552885	chr3:100346763-100346764	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs538894261	chr3:100346808-100346809	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs147136338	chr3:100346823-100346824	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs140236120	chr3:100346880-100346881	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs185471181	chr3:100346954-100346955	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs554631813	chr3:100346956-100346957	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs576174449	chr3:100346957-100346958	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs75406692	chr3:100347003-100347004	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs145659395	chr3:100347037-100347038	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs532386842	chr3:100347083-100347084	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs1165250	chr3:100347113-100347114	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs147314001	chr3:100347136-100347137	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs530305101	chr3:100347139-100347140	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs548545566	chr3:100347146-100347147	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs112549474	chr3:100347218-100347219	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs560942397	chr3:100347219-100347220	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs35854044	chr3:100347228-100347229	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs531466205	chr3:100347238-100347239	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs549916449	chr3:100347260-100347261	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs57010274	chr3:100347281-100347282	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs7644599	chr3:100347289-100347290	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs547632071	chr3:100347356-100347357	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs565878213	chr3:100347387-100347388	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs369189432	chr3:100347391-100347392	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs58406467	chr3:100347408-100347409	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs58351812	chr3:100347443-100347444	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs144221805	chr3:100347463-100347464	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs190863002	chr3:100347617-100347618	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs182630858	chr3:100347634-100347635	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs146543837	chr3:100347637-100347638	Enhancers 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:1794 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

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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