Variant report

Variant	nsv1013021
Chromosome Location	chr3:100340535-100427937
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1155)
CpG islands
(count:429)
Chromatin interactive
region (count:49)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1155 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:100381238-100381404	K562	blood:	n/a	n/a
2	ARID3A	chr3:100353731-100353930	K562	blood:	n/a	n/a
3	ARID3A	chr3:100353734-100354533	HepG2	liver:	n/a	n/a
4	ARID3A	chr3:100369723-100370159	K562	blood:	n/a	n/a
5	ARID3A	chr3:100400484-100400645	HepG2	liver:	n/a	n/a
6	ARID3A	chr3:100427756-100428585	HepG2	liver:	n/a	n/a
7	ARID3A	chr3:100359648-100359874	HepG2	liver:	n/a	n/a
8	ARID3A	chr3:100348388-100349223	K562	blood:	n/a	n/a
9	ATF1	chr3:100348373-100348950	K562	blood:	n/a	n/a
10	ATF1	chr3:100353718-100353993	K562	blood:	n/a	n/a
11	ATF2	chr3:100427777-100428567	GM12878	blood:	n/a	n/a
12	ATF2	chr3:100360476-100360923	GM12878	blood:	n/a	n/a
13	ATF2	chr3:100369506-100370238	GM12878	blood:	n/a	n/a
14	ATF3	chr3:100348592-100348961	K562	blood:	n/a	n/a
15	ATF3	chr3:100370050-100370425	K562	blood:	n/a	n/a
16	BACH1	chr3:100421452-100421833	K562	blood:	n/a	n/a
17	BACH1	chr3:100421524-100421801	H1-hESC	embryonic stem cell:	n/a	n/a
18	BACH1	chr3:100349457-100349877	H1-hESC	embryonic stem cell:	n/a	chr3:100349697-100349711
19	BACH1	chr3:100381410-100381594	K562	blood:	n/a	n/a
20	BATF	chr3:100360240-100360471	GM12878	blood:	n/a	n/a
21	BATF	chr3:100369687-100370030	GM12878	blood:	n/a	n/a
22	BATF	chr3:100369685-100370004	GM12878	blood:	n/a	n/a
23	BATF	chr3:100360218-100360885	GM12878	blood:	n/a	chr3:100360555-100360566
24	BCL11A	chr3:100360195-100360894	GM12878	blood:	n/a	n/a
25	BCL11A	chr3:100360235-100360494	GM12878	blood:	n/a	n/a
26	BCL11A	chr3:100360611-100360835	GM12878	blood:	n/a	n/a
27	BHLHE40	chr3:100427893-100428554	GM12878	blood:	n/a	chr3:100428533-100428549
28	BHLHE40	chr3:100353686-100354022	GM12878	blood:	n/a	n/a
29	BHLHE40	chr3:100353702-100354034	K562	blood:	n/a	n/a
30	BHLHE40	chr3:100353728-100354019	HepG2	liver:	n/a	n/a
31	BHLHE40	chr3:100369647-100370331	GM12878	blood:	n/a	n/a
32	BHLHE40	chr3:100360142-100360910	GM12878	blood:	n/a	n/a
33	BRCA1	chr3:100427800-100428582	H1-hESC	embryonic stem cell:	n/a	n/a
34	BRCA1	chr3:100427866-100428531	GM12878	blood:	n/a	n/a
35	BRCA1	chr3:100427676-100428558	Hela-S3	cervix:	n/a	n/a
36	CBX3	chr3:100415727-100416040	K562	blood:	n/a	n/a
37	CBX3	chr3:100427818-100428510	K562	blood:	n/a	n/a
38	CCNT2	chr3:100348632-100349219	K562	blood:	n/a	n/a
39	CCNT2	chr3:100427839-100429006	K562	blood:	n/a	chr3:100428771-100428780 chr3:100428796-100428805
40	CEBPB	chr3:100385548-100385946	K562	blood:	n/a	chr3:100385738-100385749
41	CEBPB	chr3:100420286-100420585	IMR90	lung:	n/a	n/a
42	CEBPB	chr3:100385579-100385925	Hela-S3	cervix:	n/a	chr3:100385738-100385749
43	CEBPB	chr3:100384545-100384598	K562	blood:	n/a	chr3:100384580-100384591
44	CEBPB	chr3:100385583-100385937	K562	blood:	n/a	chr3:100385738-100385749
45	CEBPB	chr3:100381321-100381668	Hela-S3	cervix:	n/a	n/a
46	CEBPB	chr3:100350095-100350440	Hela-S3	cervix:	n/a	n/a
47	CEBPB	chr3:100353821-100353823	Hela-S3	cervix:	n/a	n/a
48	CEBPB	chr3:100370681-100370923	A549	lung:	n/a	n/a
49	CEBPB	chr3:100373432-100373699	A549	lung:	n/a	chr3:100373575-100373586
50	CEBPB	chr3:100385592-100385797	K562	blood:	n/a	chr3:100385738-100385749

(count:429 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:100401284-100401334	PFSK-1	brain:	n/a
2	chr3:100427239-100427289	AG09309	skin:	n/a
3	chr3:100401284-100401334	PFSK-1	brain:	n/a
4	chr3:100427239-100427289	AG09309	skin:	n/a
5	chr3:100427096-100427146	RPTEC	kidney:	n/a
6	chr3:100427239-100427289	GM12891	blood:	n/a
7	chr3:100401284-100401334	HNPCEpiC	eye:	n/a
8	chr3:100401270-100401320	CMK	blood:	n/a
9	chr3:100401200-100401250	HMEC	breast:	n/a
10	chr3:100401284-100401334	RPTEC	kidney:	n/a
11	chr3:100349374-100349424	GM06990	blood:	n/a
12	chr3:100427239-100427289	HCF	heart:	n/a
13	chr3:100401270-100401320	ECC-1	luminal epithelium:	n/a
14	chr3:100401200-100401250	SK-N-MC	brain:	n/a
15	chr3:100424830-100424880	HRPEpiC	eye:	n/a
16	chr3:100401270-100401320	HCF	heart:	n/a
17	chr3:100427239-100427289	HepG2	liver:	n/a
18	chr3:100427239-100427289	HAEpiC	amniotic membrane:	n/a
19	chr3:100349374-100349424	Hela-S3	cervix:	n/a
20	chr3:100401270-100401320	HNPCEpiC	eye:	n/a
21	chr3:100427096-100427146	HL-60	blood:	n/a
22	chr3:100427239-100427289	SK-N-MC	brain:	n/a
23	chr3:100427096-100427146	SKMC	muscle:	n/a
24	chr3:100401284-100401334	NT2-D1	testis:	n/a
25	chr3:100401200-100401250	CMK	blood:	n/a
26	chr3:100349374-100349424	HCPEpiC	choroid plexus:	n/a
27	chr3:100349374-100349424	HRCEpiC	kidney:	n/a
28	chr3:100427096-100427146	PrEC	prostate:	n/a
29	chr3:100401200-100401250	ovcar-3	ovarian:	n/a
30	chr3:100349374-100349424	NHBE	bronchial:	n/a
31	chr3:100401270-100401320	PrEC	prostate:	n/a
32	chr3:100401270-100401320	HPAEpiC	pulmonary alveolar:	n/a
33	chr3:100424830-100424880	HCF	heart:	n/a
34	chr3:100427239-100427289	PANC-1	pancreas:	n/a
35	chr3:100401200-100401250	ECC-1	luminal epithelium:	n/a
36	chr3:100401200-100401250	NB4	blood:	n/a
37	chr3:100401200-100401250	Hepatocyte	liver:	n/a
38	chr3:100427239-100427289	AG10803	skin:	n/a
39	chr3:100427096-100427146	HUVEC	blood vessel:	n/a
40	chr3:100424830-100424880	PFSK-1	brain:	n/a
41	chr3:100427239-100427289	ECC-1	luminal epithelium:	n/a
42	chr3:100427096-100427146	HCT-116	colon:	n/a
43	chr3:100401284-100401334	A549	lung:	n/a
44	chr3:100401200-100401250	HUVEC	blood vessel:	n/a
45	chr3:100349374-100349424	SAEC	small airway:	n/a
46	chr3:100401270-100401320	AG09309	skin:	n/a
47	chr3:100427239-100427289	ProgFib	skin:	n/a
48	chr3:100401284-100401334	Caco-2	colon:	n/a
49	chr3:100401270-100401320	Caco-2	colon:	n/a
50	chr3:100427239-100427289	PFSK-1	brain:	n/a

(count:49 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:100181696..100182432-chr3:100355242..100355805,2	MCF-7	breast:
2	chr3:100421148..100423017-chr3:100443429..100446212,2	K562	blood:
3	chr3:100427232..100427732-chr9:96215167..96215670,2	Hela-S3	cervix:
4	chr3:100348848..100350778-chr3:100351417..100355406,3	K562	blood:
5	chr3:100414154..100421316-chr3:100422241..100429195,9	MCF-7	breast:
6	chr3:100322114..100322780-chr3:100353316..100353989,3	MCF-7	breast:
7	chr3:100367436..100369530-chr3:100426605..100429472,2	MCF-7	breast:
8	chr1:73273811..73275334-chr3:100425817..100428133,2	MCF-7	breast:
9	chr20:33543190..33544135-chr3:100427443..100428252,2	NB4	blood:
10	chr3:100372478..100376338-chr3:100378859..100382078,3	K562	blood:
11	chr3:100355413..100357441-chr3:100427541..100429664,2	K562	blood:
12	chr18:3247419..3248282-chr3:100427656..100428171,2	Hela-S3	cervix:
13	chr3:100415596..100419109-chr3:100421112..100424187,4	K562	blood:
14	chr3:100279818..100281392-chr3:100419411..100421780,2	K562	blood:
15	chr3:100412000..100414603-chr3:100428096..100429901,2	K562	blood:
16	chr3:100412832..100415800-chr3:100417725..100420372,2	K562	blood:
17	chr3:100352243..100354477-chr3:100424707..100427239,2	MCF-7	breast:
18	chr3:100419538..100421699-chr3:100430283..100434420,3	MCF-7	breast:
19	chr3:100410212..100413199-chr3:100413505..100415346,2	K562	blood:
20	chr3:100369607..100371401-chr3:100374454..100376110,2	K562	blood:
21	chr3:100340717..100343040-chr3:100348395..100351881,3	K562	blood:
22	chr3:100374838..100376761-chr3:100378684..100380359,2	K562	blood:
23	chr3:100321003..100323549-chr3:100347554..100350487,3	MCF-7	breast:
24	chr3:100358087..100360713-chr3:100362813..100364716,2	K562	blood:
25	chr3:100120411..100122999-chr3:100364924..100367578,2	K562	blood:
26	chr3:100417750..100419779-chr3:100427601..100429655,2	K562	blood:
27	chr3:100118702..100121299-chr3:100427057..100432444,4	K562	blood:
28	chr3:100118924..100121912-chr3:100362623..100364573,2	K562	blood:
29	chr3:100423356..100425214-chr3:100428038..100429852,2	K562	blood:
30	chr3:100348848..100350394-chr3:100351417..100354134,2	K562	blood:
31	chr3:100325466..100327241-chr3:100349090..100350621,2	K562	blood:
32	chr3:100325886..100329093-chr3:100426560..100431642,4	MCF-7	breast:
33	chr3:100120818..100123698-chr3:100370041..100372201,2	K562	blood:
34	chr3:100374838..100376761-chr3:100378684..100380359,2	K562	blood:
35	chr3:100369607..100371401-chr3:100374454..100376110,2	K562	blood:
36	chr3:100364940..100366707-chr3:100366782..100369483,3	K562	blood:
37	chr3:100321992..100322818-chr3:100353419..100354308,2	MCF-7	breast:
38	chr17:57918588..57920867-chr3:100426772..100429347,2	MCF-7	breast:
39	chr3:100420077..100423053-chr3:100428087..100429810,2	MCF-7	breast:
40	chr3:100181153..100182757-chr3:100352927..100354311,7	MCF-7	breast:
41	chr3:100348848..100350394-chr3:100351417..100354134,2	K562	blood:
42	chr3:100325407..100326196-chr3:100353394..100354270,2	MCF-7	breast:
43	chr3:100419966..100423130-chr3:100426813..100428964,3	K562	blood:
44	chr3:100415596..100419109-chr3:100421112..100424187,4	K562	blood:
45	chr3:100340717..100343040-chr3:100348395..100351881,3	K562	blood:
46	chr3:100412832..100415800-chr3:100417725..100420372,2	K562	blood:
47	chr3:100353552..100356244-chr3:100358458..100360777,2	K562	blood:
48	chr3:100358087..100360713-chr3:100362813..100364716,2	K562	blood:
49	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
ENSG00000188938	chromatin interactions
ENSG00000154174	chromatin interactions
ENSG00000101608	chromatin interactions
ENSG00000199004	chromatin interactions
ENSG00000252989	chromatin interactions
ENSG00000114354	chromatin interactions
ENSG00000206535	chromatin interactions
ENSG00000144820	chromatin interactions
ENSG00000100983	chromatin interactions

Extended variants
information (count: 3514 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:3514 , 50 per page) page: 1 2 3 4 5 6 7 ... 71

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs192423994	chr3:100340540-100340541	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs185710075	chr3:100340598-100340599	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs531034982	chr3:100340602-100340603	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs549857672	chr3:100340629-100340630	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs571377152	chr3:100340657-100340658	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs538626620	chr3:100340713-100340714	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs553846518	chr3:100340731-100340732	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs531529140	chr3:100340771-100340772	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs1620897	chr3:100340796-100340797	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs145973729	chr3:100340820-100340821	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs9821668	chr3:100340827-100340828	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs532460652	chr3:100340828-100340829	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs547146887	chr3:100340832-100340833	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs188637140	chr3:100340852-100340853	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs142075383	chr3:100340897-100340898	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs576971936	chr3:100340922-100340923	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs568023239	chr3:100340941-100340942	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs559732959	chr3:100340957-100340958	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs536085382	chr3:100341021-100341022	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs74508526	chr3:100341064-100341065	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs140675087	chr3:100341109-100341110	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs397990633	chr3:100341123-100341124	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs61022302	chr3:100341129-100341130	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs114261972	chr3:100341135-100341136	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs192904533	chr3:100341154-100341155	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs151138622	chr3:100341197-100341198	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs114230351	chr3:100341199-100341200	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs571358919	chr3:100341226-100341227	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs532270708	chr3:100341246-100341247	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs77604998	chr3:100341304-100341305	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs569765311	chr3:100341343-100341344	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs659080	chr3:100341346-100341347	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs536605355	chr3:100341419-100341420	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs376791953	chr3:100341447-100341448	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs79696346	chr3:100341481-100341482	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs567222862	chr3:100341503-100341504	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs554800000	chr3:100341513-100341514	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs577416691	chr3:100341520-100341521	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs149850727	chr3:100341564-100341565	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs536845688	chr3:100341565-100341566	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs147944218	chr3:100341612-100341613	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs184717633	chr3:100341634-100341635	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs570201917	chr3:100341640-100341641	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs141768250	chr3:100341652-100341653	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs553215666	chr3:100341697-100341698	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs574730885	chr3:100341708-100341709	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs147081069	chr3:100341715-100341716	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs188737678	chr3:100341742-100341743	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs147701097	chr3:100341743-100341744	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs546394886	chr3:100341755-100341756	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:711 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:100339600-100340800	Enhancers	Small Intestine	intestine
2	chr3:100339800-100343000	Weak transcription	Fetal Intestine Large	intestine
3	chr3:100340000-100341800	Weak transcription	Fetal Intestine Small	intestine
4	chr3:100340800-100341000	Weak transcription	Small Intestine	intestine
5	chr3:100340800-100341200	Enhancers	K562	blood
6	chr3:100341800-100342000	ZNF genes & repeats	Fetal Intestine Small	intestine
7	chr3:100343800-100352000	Weak transcription	Fetal Intestine Large	intestine
8	chr3:100346200-100348000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr3:100346400-100348200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
10	chr3:100347400-100347600	Enhancers	Small Intestine	intestine
11	chr3:100347400-100348600	Enhancers	Primary hematopoietic stem cells	blood
12	chr3:100347600-100349200	Weak transcription	Small Intestine	intestine
13	chr3:100347600-100350000	Enhancers	HUVEC	blood vessel
14	chr3:100347600-100350400	Enhancers	K562	blood
15	chr3:100347800-100349800	Enhancers	Primary hematopoietic stem cells short term culture	blood
16	chr3:100348000-100348800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr3:100348200-100348600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
18	chr3:100348200-100349800	Enhancers	NHEK	skin
19	chr3:100348200-100352200	Weak transcription	Primary neutrophils fromperipheralblood	blood
20	chr3:100348400-100349200	Enhancers	Duodenum Mucosa	Duodenum
21	chr3:100348400-100349400	Enhancers	Fetal Intestine Small	intestine
22	chr3:100348400-100350600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
23	chr3:100348400-100350600	Enhancers	HMEC	breast
24	chr3:100348600-100349800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
25	chr3:100348600-100350200	Enhancers	Hela-S3	cervix
26	chr3:100348600-100350400	Enhancers	HUES64 Cell Line	embryonic stem cell
27	chr3:100348600-100353400	Weak transcription	Primary hematopoietic stem cells	blood
28	chr3:100348600-100354200	Weak transcription	Sigmoid Colon	Sigmoid Colon
29	chr3:100348800-100349800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chr3:100349000-100350400	Enhancers	iPS-15b Cell Line	embryonic stem cell
31	chr3:100349000-100350600	Enhancers	ES-I3 Cell Line	embryonic stem cell
32	chr3:100349000-100350600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
33	chr3:100349200-100349400	Enhancers	Small Intestine	intestine
34	chr3:100349200-100350200	Enhancers	A549	lung
35	chr3:100349200-100350400	Enhancers	HUES6 Cell Line	embryonic stem cell
36	chr3:100349200-100350400	Enhancers	iPS-18 Cell Line	embryonic stem cell
37	chr3:100349200-100350600	Enhancers	iPS-20b Cell Line	embryonic stem cell
38	chr3:100349200-100352400	Weak transcription	Duodenum Mucosa	Duodenum
39	chr3:100349400-100352800	Weak transcription	Fetal Intestine Small	intestine
40	chr3:100349600-100349800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr3:100349600-100349800	Bivalent Enhancer	NHDF-Ad	bronchial
42	chr3:100349600-100350400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
43	chr3:100349600-100350400	Enhancers	H9 Cell Line	embryonic stem cell
44	chr3:100349800-100350000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr3:100349800-100352600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
46	chr3:100349800-100352800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
47	chr3:100349800-100352800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
48	chr3:100350400-100353600	Weak transcription	K562	blood
49	chr3:100350600-100353600	Weak transcription	HMEC	breast
50	chr3:100350600-100354000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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