Variant report

Variant	nsv460770
Chromosome Location	chr3:100310812-100433592
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2188)
CpG islands
(count:1588)
Chromatin interactive
region (count:71)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2188 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:100332649-100333246	HepG2	liver:	n/a	n/a
2	ARID3A	chr3:100359648-100359874	HepG2	liver:	n/a	n/a
3	ARID3A	chr3:100321800-100321832	K562	blood:	n/a	n/a
4	ARID3A	chr3:100427756-100428585	HepG2	liver:	n/a	n/a
5	ARID3A	chr3:100353731-100353930	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	chr3:100381238-100381404	K562	blood:	n/a	n/a
9	ARID3A	chr3:100321365-100321737	HepG2	liver:	n/a	n/a
10	ARID3A	chr3:100328325-100328363	K562	blood:	n/a	n/a
11	ARID3A	chr3:100428405-100428550	K562	blood:	n/a	n/a
12	ARID3A	chr3:100400484-100400645	HepG2	liver:	n/a	n/a
13	ARID3A	chr3:100348388-100349223	K562	blood:	n/a	n/a
14	ATF1	chr3:100348373-100348950	K562	blood:	n/a	n/a
15	ATF1	chr3:100328075-100328453	K562	blood:	n/a	n/a
16	ATF1	chr3:100427978-100428440	K562	blood:	n/a	n/a
17	ATF1	chr3:100353718-100353993	K562	blood:	n/a	n/a
18	ATF2	chr3:100427777-100428567	GM12878	blood:	n/a	n/a
19	ATF2	chr3:100360476-100360923	GM12878	blood:	n/a	n/a
20	ATF2	chr3:100369506-100370238	GM12878	blood:	n/a	n/a
21	ATF2	chr3:100429275-100429952	GM12878	blood:	n/a	n/a
22	ATF3	chr3:100370050-100370425	K562	blood:	n/a	n/a
23	ATF3	chr3:100348592-100348961	K562	blood:	n/a	n/a
24	BACH1	chr3:100324408-100324438	H1-hESC	embryonic stem cell:	n/a	n/a
25	BACH1	chr3:100421452-100421833	K562	blood:	n/a	n/a
26	BACH1	chr3:100321333-100321898	K562	blood:	n/a	n/a
27	BACH1	chr3:100421524-100421801	H1-hESC	embryonic stem cell:	n/a	n/a
28	BACH1	chr3:100428023-100428678	H1-hESC	embryonic stem cell:	n/a	n/a
29	BACH1	chr3:100321277-100321953	H1-hESC	embryonic stem cell:	n/a	n/a
30	BACH1	chr3:100349457-100349877	H1-hESC	embryonic stem cell:	n/a	chr3:100349697-100349711
31	BACH1	chr3:100381410-100381594	K562	blood:	n/a	n/a
32	BATF	chr3:100429333-100429812	GM12878	blood:	n/a	n/a
33	BATF	chr3:100360218-100360885	GM12878	blood:	n/a	chr3:100360555-100360566
34	BATF	chr3:100369685-100370004	GM12878	blood:	n/a	n/a
35	BATF	chr3:100360240-100360471	GM12878	blood:	n/a	n/a
36	BATF	chr3:100369687-100370030	GM12878	blood:	n/a	n/a
37	BATF	chr3:100429220-100429801	GM12878	blood:	n/a	n/a
38	BCL11A	chr3:100360195-100360894	GM12878	blood:	n/a	n/a
39	BCL11A	chr3:100360235-100360494	GM12878	blood:	n/a	n/a
40	BCL11A	chr3:100360611-100360835	GM12878	blood:	n/a	n/a
41	BCLAF1	chr3:100325837-100326298	GM12878	blood:	n/a	n/a
42	BCLAF1	chr3:100428169-100428667	GM12878	blood:	n/a	chr3:100428545-100428558 chr3:100428541-100428554 chr3:100428539-100428552
43	BCLAF1	chr3:100322205-100322553	GM12878	blood:	n/a	n/a
44	BCLAF1	chr3:100429350-100429879	GM12878	blood:	n/a	chr3:100429694-100429703 chr3:100429744-100429753 chr3:100429743-100429752
45	BHLHE40	chr3:100427985-100428525	K562	blood:	n/a	n/a
46	BHLHE40	chr3:100428011-100428266	A549	lung:	n/a	n/a
47	BHLHE40	chr3:100427970-100428628	HepG2	liver:	n/a	chr3:100428533-100428549
48	BHLHE40	chr3:100427893-100428554	GM12878	blood:	n/a	chr3:100428533-100428549
49	BHLHE40	chr3:100360142-100360910	GM12878	blood:	n/a	n/a
50	BHLHE40	chr3:100353702-100354034	K562	blood:	n/a	n/a

(count:1588 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:100428147-100428197	HMEC	breast:	n/a
2	chr3:100322629-100322679	U87	brain:	n/a
3	chr3:100428147-100428197	HMEC	breast:	n/a
4	chr3:100322629-100322679	U87	brain:	n/a
5	chr3:100428033-100428083	ovcar-3	ovarian:	n/a
6	chr3:100349374-100349424	AG09309	skin:	n/a
7	chr3:100428005-100428055	HCPEpiC	choroid plexus:	n/a
8	chr3:100401270-100401320	HCF	heart:	n/a
9	chr3:100401270-100401320	GM12878	blood:	n/a
10	chr3:100328186-100328236	HRCEpiC	kidney:	n/a
11	chr3:100428147-100428197	HEEpiC	esophagus:	n/a
12	chr3:100328745-100328795	HCF	heart:	n/a
13	chr3:100328713-100328763	HPAEpiC	pulmonary alveolar:	n/a
14	chr3:100401270-100401320	Hepatocyte	liver:	n/a
15	chr3:100428145-100428195	Caco-2	colon:	n/a
16	chr3:100328186-100328236	IMR90	lung:	fetal
17	chr3:100401200-100401250	HEEpiC	esophagus:	n/a
18	chr3:100428172-100428222	NH-A	brain:	n/a
19	chr3:100328713-100328763	NHDF-neo	bronchial:	n/a
20	chr3:100428172-100428222	NHDF-neo	bronchial:	n/a
21	chr3:100328186-100328236	AoSMC	blood vessel:	n/a
22	chr3:100428033-100428083	HMEC	breast:	n/a
23	chr3:100327897-100327947	Caco-2	colon:	n/a
24	chr3:100428140-100428190	SK-N-SH_RA	brain:	n/a
25	chr3:100428070-100428120	GM12891	blood:	n/a
26	chr3:100401200-100401250	ovcar-3	ovarian:	n/a
27	chr3:100428398-100428448	Hela-S3	cervix:	n/a
28	chr3:100349374-100349424	PrEC	prostate:	n/a
29	chr3:100322629-100322679	HAEpiC	amniotic membrane:	n/a
30	chr3:100401200-100401250	SAEC	small airway:	n/a
31	chr3:100430811-100430861	NB4	blood:	n/a
32	chr3:100327897-100327947	GM12891	blood:	n/a
33	chr3:100428642-100428692	K562	blood:	n/a
34	chr3:100328265-100328315	HCT-116	colon:	n/a
35	chr3:100428172-100428222	GM12892	blood:	n/a
36	chr3:100428033-100428083	Jurkat	blood:	n/a
37	chr3:100327897-100327947	HCT-116	colon:	n/a
38	chr3:100429064-100429114	NHDF-neo	bronchial:	n/a
39	chr3:100428147-100428197	H1-hESC	embryonic stem cell:	embryo
40	chr3:100429064-100429114	GM12891	blood:	n/a
41	chr3:100349374-100349424	AG04449	skin:	fetal
42	chr3:100428869-100428919	HRPEpiC	eye:	n/a
43	chr3:100428642-100428692	SK-N-SH_RA	brain:	n/a
44	chr3:100428869-100428919	HIPEpiC	eye:	n/a
45	chr3:100428033-100428083	NT2-D1	testis:	n/a
46	chr3:100328713-100328763	HepG2	liver:	n/a
47	chr3:100322493-100322543	ovcar-3	ovarian:	n/a
48	chr3:100401284-100401334	HEK293	kidney:	embryo
49	chr3:100424830-100424880	HCF	heart:	n/a
50	chr3:100401200-100401250	NT2-D1	testis:	n/a

(count:71 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr3:100325407..100326196-chr3:100353394..100354270,2	MCF-7	breast:
2	chr3:100321992..100322818-chr3:100353419..100354308,2	MCF-7	breast:
3	chr3:100369607..100371401-chr3:100374454..100376110,2	K562	blood:
4	chr3:100348848..100350778-chr3:100351417..100355406,3	K562	blood:
5	chr3:100355413..100357441-chr3:100427541..100429664,2	K562	blood:
6	chr3:100118924..100121912-chr3:100362623..100364573,2	K562	blood:
7	chr3:100417750..100419779-chr3:100427601..100429655,2	K562	blood:
8	chr3:100419966..100423130-chr3:100426813..100428964,3	K562	blood:
9	chr3:100120818..100123698-chr3:100370041..100372201,2	K562	blood:
10	chr3:100419538..100421699-chr3:100430283..100434420,3	MCF-7	breast:
11	chr3:100428095..100432338-chr3:100432996..100435628,5	K562	blood:
12	chr3:100181722..100182327-chr3:100321776..100322610,2	MCF-7	breast:
13	chr3:100412832..100415800-chr3:100417725..100420372,2	K562	blood:
14	chr3:100374838..100376761-chr3:100378684..100380359,2	K562	blood:
15	chr3:100340717..100343040-chr3:100348395..100351881,3	K562	blood:
16	chr3:100423356..100425214-chr3:100428038..100429852,2	K562	blood:
17	chr3:100118702..100121299-chr3:100427057..100432444,4	K562	blood:
18	chr3:100321003..100323549-chr3:100347554..100350487,3	MCF-7	breast:
19	chr3:100322090..100322923-chr3:100479827..100480358,2	MCF-7	breast:
20	chr3:100432846..100436544-chr3:100436912..100439975,5	K562	blood:
21	chr3:100374838..100376761-chr3:100378684..100380359,2	K562	blood:
22	chr3:100410212..100413199-chr3:100413505..100415346,2	K562	blood:
23	chr3:100372478..100376338-chr3:100378859..100382078,3	K562	blood:
24	chr1:73273811..73275334-chr3:100425817..100428133,2	MCF-7	breast:
25	chr3:100428105..100429880-chr3:100429992..100431694,2	K562	blood:
26	chr18:3247419..3248282-chr3:100427656..100428171,2	Hela-S3	cervix:
27	chr3:100425991..100429784-chr3:100429994..100431694,4	K562	blood:
28	chr11:59436077..59436715-chr3:100428082..100428818,2	Hela-S3	cervix:
29	chr3:100358087..100360713-chr3:100362813..100364716,2	K562	blood:
30	chr3:100325886..100329093-chr3:100426560..100431642,4	MCF-7	breast:
31	chr3:100340717..100343040-chr3:100348395..100351881,3	K562	blood:
32	chr3:100369607..100371401-chr3:100374454..100376110,2	K562	blood:
33	chr3:100321003..100323549-chr3:100347554..100350487,3	MCF-7	breast:
34	chr3:100364940..100366707-chr3:100366782..100369483,3	K562	blood:
35	chr1:151512640..151513443-chr3:100428519..100429048,2	Hela-S3	cervix:
36	chr3:100118375..100121332-chr3:100329278..100332064,2	K562	blood:
37	chr3:100410212..100413199-chr3:100413505..100415346,2	K562	blood:
38	chr3:100348848..100350394-chr3:100351417..100354134,2	K562	blood:
39	chr3:100325466..100327241-chr3:100349090..100350621,2	K562	blood:
40	chr3:100352243..100354477-chr3:100424707..100427239,2	MCF-7	breast:
41	chr3:100322114..100322780-chr3:100353316..100353989,3	MCF-7	breast:
42	chr3:100322069..100322963-chr3:100515153..100515789,2	MCF-7	breast:
43	chr3:100325886..100329093-chr3:100426560..100431642,4	MCF-7	breast:
44	chr3:100415596..100419109-chr3:100421112..100424187,4	K562	blood:
45	chr3:100322114..100322780-chr3:100353316..100353989,3	MCF-7	breast:
46	chr3:100321992..100322818-chr3:100353419..100354308,2	MCF-7	breast:
47	chr3:100414154..100421316-chr3:100422241..100429195,9	MCF-7	breast:
48	chr3:100419538..100421699-chr3:100430283..100434420,3	MCF-7	breast:
49	chr3:100325466..100327241-chr3:100349090..100350621,2	K562	blood:
50	chr3:100432153..100434876-chr3:100437236..100438974,2	MCF-7	breast:

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

Extended variants
information (count: 4948 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:4948 , 50 per page) page: 1 2 3 4 5 6 7 ... 99

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6786853	chr3:100310812-100310813	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs190880583	chr3:100310834-100310835	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs551059329	chr3:100310841-100310842	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs56239206	chr3:100310849-100310850	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs557271915	chr3:100310892-100310893	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs76082045	chr3:100310926-100310927	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs575837148	chr3:100310928-100310929	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs543127594	chr3:100310947-100310948	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs527937863	chr3:100310957-100310958	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs549644408	chr3:100310960-100310961	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs182638681	chr3:100310985-100310986	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs534630264	chr3:100310989-100310990	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs559393257	chr3:100310996-100310997	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs80088363	chr3:100311010-100311011	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs58681466	chr3:100311023-100311024	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs569737734	chr3:100311031-100311032	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs530762805	chr3:100311077-100311078	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs552109861	chr3:100311078-100311079	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs567913021	chr3:100311087-100311088	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs552931562	chr3:100311117-100311118	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs59083168	chr3:100311137-100311138	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs59480627	chr3:100311140-100311141	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs570891046	chr3:100311169-100311170	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs548066226	chr3:100311170-100311171	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs150816604	chr3:100311184-100311185	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs568165095	chr3:100311242-100311243	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs535739124	chr3:100311256-100311257	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs368941570	chr3:100311263-100311264	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs1165521	chr3:100311264-100311265	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs9290098	chr3:100311265-100311266	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs112294130	chr3:100311274-100311275	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs539986831	chr3:100311307-100311308	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs187268611	chr3:100311318-100311319	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs1165522	chr3:100311349-100311350	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs190955172	chr3:100311374-100311375	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs9290099	chr3:100311377-100311378	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs138101913	chr3:100311398-100311399	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs9790050	chr3:100311439-100311440	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs572414153	chr3:100311448-100311449	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs9790219	chr3:100311453-100311454	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs9790137	chr3:100311489-100311490	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs574018420	chr3:100311533-100311534	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs544387082	chr3:100311542-100311543	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs562691822	chr3:100311571-100311572	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs9290100	chr3:100311596-100311597	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs149531671	chr3:100311681-100311682	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs183521677	chr3:100311702-100311703	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs146011250	chr3:100311707-100311708	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs528564353	chr3:100311725-100311726	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs546731745	chr3:100311727-100311728	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:62)

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	22037309	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:1643 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:100308800-100312000	Enhancers	Fetal Intestine Large	intestine
2	chr3:100309200-100311000	Enhancers	Rectal Mucosa Donor 31	rectum
3	chr3:100309200-100312000	Enhancers	Fetal Intestine Small	intestine
4	chr3:100309600-100311000	Enhancers	A549	lung
5	chr3:100310200-100311000	Enhancers	Rectal Mucosa Donor 29	rectum
6	chr3:100310800-100311600	Enhancers	Liver	Liver
7	chr3:100310800-100319200	Weak transcription	Duodenum Mucosa	Duodenum
8	chr3:100311600-100313600	Weak transcription	Liver	Liver
9	chr3:100313600-100314600	Enhancers	Liver	Liver
10	chr3:100318200-100324200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
11	chr3:100318600-100318800	Enhancers	NHEK	skin
12	chr3:100318600-100319000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
13	chr3:100318600-100319200	Enhancers	Dnd41	blood
14	chr3:100318600-100319600	Enhancers	Primary T cells from cord blood	blood
15	chr3:100318600-100320600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr3:100318800-100319400	Flanking Active TSS	NHEK	skin
17	chr3:100318800-100319800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
18	chr3:100318800-100323200	Enhancers	HMEC	breast
19	chr3:100319000-100319400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
20	chr3:100319000-100319400	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
21	chr3:100319000-100319600	Enhancers	Primary T helper cells PMA-I stimulated	--
22	chr3:100319000-100319600	Enhancers	Thymus	Thymus
23	chr3:100319000-100320000	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr3:100319000-100320600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr3:100319000-100323000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr3:100319200-100319400	Enhancers	Primary T cells fromperipheralblood	blood
27	chr3:100319200-100319400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
28	chr3:100319200-100319400	Enhancers	Primary T killer memory cells from peripheral blood	blood
29	chr3:100319200-100319400	Enhancers	Rectal Mucosa Donor 31	rectum
30	chr3:100319200-100319600	Enhancers	Primary hematopoietic stem cells short term culture	blood
31	chr3:100319200-100319600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
32	chr3:100319200-100319600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
33	chr3:100319200-100319800	Enhancers	Primary T helper naive cells from peripheral blood	blood
34	chr3:100319200-100319800	Enhancers	Primary T helper cells fromperipheralblood	blood
35	chr3:100319200-100319800	Enhancers	Fetal Thymus	thymus
36	chr3:100319200-100319800	Flanking Active TSS	Dnd41	blood
37	chr3:100319200-100319800	Enhancers	GM12878-XiMat	blood
38	chr3:100319200-100320000	Enhancers	Esophagus	oesophagus
39	chr3:100319200-100321200	Enhancers	HepG2	liver
40	chr3:100319200-100321600	Enhancers	Duodenum Mucosa	Duodenum
41	chr3:100319400-100319600	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
42	chr3:100319400-100319600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
43	chr3:100319400-100319600	Enhancers	NHEK	skin
44	chr3:100319400-100321400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
45	chr3:100319400-100321400	Weak transcription	Rectal Mucosa Donor 31	rectum
46	chr3:100319400-100322000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
47	chr3:100319400-100322200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
48	chr3:100319600-100319800	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
49	chr3:100319600-100319800	Enhancers	Stomach Mucosa	stomach
50	chr3:100319600-100320200	Flanking Active TSS	NHEK	skin

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