Variant report

Variant	esv1799124
Chromosome Location	chr3:113426201-113468350
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1849)
CpG islands
(count:1037)
Chromatin interactive
region (count:74)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:5)

(count:1849 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:113463954-113464440	HepG2	liver:	n/a	n/a
2	ARID3A	chr3:113465251-113465963	K562	blood:	n/a	n/a
3	ARID3A	chr3:113462067-113462230	HepG2	liver:	n/a	n/a
4	ARID3A	chr3:113463168-113463170	HepG2	liver:	n/a	n/a
5	ARID3A	chr3:113464720-113465818	HepG2	liver:	n/a	n/a
6	ARID3A	chr3:113455366-113455594	K562	blood:	n/a	n/a
7	ARID3A	chr3:113455354-113456163	HepG2	liver:	n/a	n/a
8	ARID3A	chr3:113468024-113468260	K562	blood:	n/a	n/a
9	ARID3A	chr3:113464738-113464752	K562	blood:	n/a	n/a
10	ATF1	chr3:113464990-113465790	K562	blood:	n/a	n/a
11	ATF2	chr3:113466071-113466870	GM12878	blood:	n/a	n/a
12	ATF2	chr3:113463811-113464435	GM12878	blood:	n/a	chr3:113463938-113463945 chr3:113464029-113464036
13	ATF2	chr3:113464978-113465907	GM12878	blood:	n/a	n/a
14	ATF2	chr3:113464910-113465829	H1-hESC	embryonic stem cell:	n/a	n/a
15	ATF2	chr3:113455321-113455709	GM12878	blood:	n/a	n/a
16	ATF2	chr3:113464953-113465849	GM12878	blood:	n/a	n/a
17	ATF2	chr3:113464992-113465750	H1-hESC	embryonic stem cell:	n/a	n/a
18	ATF3	chr3:113464986-113465726	GM12878	blood:	n/a	chr3:113465543-113465552
19	ATF3	chr3:113464878-113465815	A549	lung:	n/a	chr3:113465543-113465552
20	ATF3	chr3:113464940-113465212	K562	blood:	n/a	n/a
21	ATF3	chr3:113465449-113465780	K562	blood:	n/a	chr3:113465543-113465552
22	ATF3	chr3:113465425-113465620	K562	blood:	n/a	chr3:113465543-113465552
23	BACH1	chr3:113464031-113464318	H1-hESC	embryonic stem cell:	n/a	n/a
24	BACH1	chr3:113464720-113464914	H1-hESC	embryonic stem cell:	n/a	n/a
25	BACH1	chr3:113431132-113431186	H1-hESC	embryonic stem cell:	n/a	n/a
26	BACH1	chr3:113466316-113466551	H1-hESC	embryonic stem cell:	n/a	n/a
27	BATF	chr3:113462873-113463128	GM12878	blood:	n/a	chr3:113462982-113462993
28	BATF	chr3:113467800-113468066	GM12878	blood:	n/a	n/a
29	BATF	chr3:113431058-113431364	GM12878	blood:	n/a	chr3:113431210-113431221
30	BCL3	chr3:113465116-113465846	A549	lung:	n/a	n/a
31	BCL3	chr3:113462752-113463214	GM12878	blood:	n/a	n/a
32	BCL3	chr3:113430599-113431519	A549	lung:	n/a	n/a
33	BCL3	chr3:113460580-113460769	GM12878	blood:	n/a	n/a
34	BCL3	chr3:113462799-113463200	GM12878	blood:	n/a	n/a
35	BCL3	chr3:113460503-113460815	GM12878	blood:	n/a	n/a
36	BCLAF1	chr3:113463889-113464514	GM12878	blood:	n/a	chr3:113464338-113464346
37	BCLAF1	chr3:113464694-113465816	GM12878	blood:	n/a	n/a
38	BCLAF1	chr3:113465323-113465787	K562	blood:	n/a	n/a
39	BCLAF1	chr3:113466310-113466966	GM12878	blood:	n/a	chr3:113466343-113466356
40	BCLAF1	chr3:113462022-113462569	GM12878	blood:	n/a	n/a
41	BCLAF1	chr3:113464449-113465829	GM12878	blood:	n/a	chr3:113464628-113464637 chr3:113464652-113464661
42	BHLHE40	chr3:113464005-113466397	HepG2	liver:	n/a	chr3:113465543-113465552 chr3:113465537-113465558 chr3:113465541-113465554 chr3:113465543-113465552
43	BHLHE40	chr3:113464925-113465717	A549	lung:	n/a	chr3:113465543-113465552 chr3:113465537-113465558 chr3:113465541-113465554 chr3:113465543-113465552
44	BHLHE40	chr3:113463836-113466925	GM12878	blood:	n/a	chr3:113465543-113465552 chr3:113465537-113465558 chr3:113465541-113465554 chr3:113465543-113465552
45	BHLHE40	chr3:113464012-113466695	K562	blood:	n/a	chr3:113465543-113465552 chr3:113465537-113465558 chr3:113465541-113465554 chr3:113465543-113465552
46	BRCA1	chr3:113465126-113465707	H1-hESC	embryonic stem cell:	n/a	n/a
47	BRCA1	chr3:113464578-113465714	HepG2	liver:	n/a	n/a
48	BRCA1	chr3:113464451-113464503	GM12878	blood:	n/a	n/a
49	BRCA1	chr3:113464043-113464306	HepG2	liver:	n/a	n/a
50	BRCA1	chr3:113463948-113464455	Hela-S3	cervix:	n/a	n/a

(count:1037 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:113466193-113466243	T-47D	breast:	n/a
2	chr3:113465772-113465822	AG10803	skin:	n/a
3	chr3:113461489-113461539	SK-N-MC	brain:	n/a
4	chr3:113465120-113465170	AG10803	skin:	n/a
5	chr3:113465772-113465822	LNCaP	prostate:	n/a
6	chr3:113466193-113466243	Hela-S3	cervix:	n/a
7	chr3:113465629-113465679	HRCEpiC	kidney:	n/a
8	chr3:113465925-113465975	AG10803	skin:	n/a
9	chr3:113465925-113465975	MCF-7	breast:	n/a
10	chr3:113465791-113465841	HNPCEpiC	eye:	n/a
11	chr3:113464350-113464400	CMK	blood:	n/a
12	chr3:113464350-113464400	SKMC	muscle:	n/a
13	chr3:113465583-113465633	HNPCEpiC	eye:	n/a
14	chr3:113458144-113458194	GM19239	blood:	n/a
15	chr3:113465629-113465679	U87	brain:	n/a
16	chr3:113461489-113461539	T-47D	breast:	n/a
17	chr3:113464879-113464929	NT2-D1	testis:	n/a
18	chr3:113466193-113466243	HEK293	kidney:	embryo
19	chr3:113461489-113461539	HL-60	blood:	n/a
20	chr3:113461489-113461539	HEEpiC	esophagus:	n/a
21	chr3:113465803-113465853	SK-N-SH_RA	brain:	n/a
22	chr3:113458144-113458194	Hela-S3	cervix:	n/a
23	chr3:113464438-113464488	BE2_C	brain:	n/a
24	chr3:113465925-113465975	SKMC	muscle:	n/a
25	chr3:113465803-113465853	Jurkat	blood:	n/a
26	chr3:113464350-113464400	HL-60	blood:	n/a
27	chr3:113464379-113464429	HEEpiC	esophagus:	n/a
28	chr3:113464879-113464929	AG09319	gingival:	n/a
29	chr3:113458144-113458194	HEK293	kidney:	embryo
30	chr3:113439314-113439364	Jurkat	blood:	n/a
31	chr3:113458144-113458194	PFSK-1	brain:	n/a
32	chr3:113465772-113465822	Hepatocyte	liver:	n/a
33	chr3:113464438-113464488	NHBE	bronchial:	n/a
34	chr3:113466193-113466243	HRCEpiC	kidney:	n/a
35	chr3:113464879-113464929	SKMC	muscle:	n/a
36	chr3:113464350-113464400	AG04450	lung:	fetal
37	chr3:113465120-113465170	AG04449	skin:	fetal
38	chr3:113458144-113458194	Hepatocyte	liver:	n/a
39	chr3:113465791-113465841	HCF	heart:	n/a
40	chr3:113458144-113458194	ProgFib	skin:	n/a
41	chr3:113465791-113465841	LNCaP	prostate:	n/a
42	chr3:113464993-113465043	AoSMC	blood vessel:	n/a
43	chr3:113464379-113464429	HIPEpiC	eye:	n/a
44	chr3:113466193-113466243	MCF-7	breast:	n/a
45	chr3:113439314-113439364	HEK293	kidney:	embryo
46	chr3:113465925-113465975	SK-N-SH	brain:	n/a
47	chr3:113464993-113465043	PFSK-1	brain:	n/a
48	chr3:113464379-113464429	HNPCEpiC	eye:	n/a
49	chr3:113465120-113465170	HAEpiC	amniotic membrane:	n/a
50	chr3:113464993-113465043	SK-N-SH	brain:	n/a

(count:74 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr3:113441473..113444141-chr3:113463722..113467247,4	MCF-7	breast:
2	chr3:113454872..113455949-chr3:113463185..113464560,4	MCF-7	breast:
3	chr3:113465900..113466497-chr5:154237069..154238012,2	Hela-S3	cervix:
4	chr3:113250521..113252326-chr3:113465017..113467077,2	MCF-7	breast:
5	chr3:113465135..113465678-chr5:151150504..151151260,2	NB4	blood:
6	chr13:111805904..111806500-chr3:113465040..113465690,2	NB4	blood:
7	chr3:113449396..113451333-chr3:113460662..113462538,2	MCF-7	breast:
8	chr3:113454439..113456522-chr3:113456826..113458357,2	MCF-7	breast:
9	chr3:113414198..113416017-chr3:113464924..113466607,2	MCF-7	breast:
10	chr3:113440653..113444189-chr3:113444738..113447861,4	K562	blood:
11	chr3:113455057..113455827-chr3:113874053..113874702,2	MCF-7	breast:
12	chr3:113437875..113440758-chr3:113442135..113445039,2	MCF-7	breast:
13	chr3:113419849..113421938-chr3:113437398..113440132,2	MCF-7	breast:
14	chr3:113449046..113452860-chr3:113462915..113466882,4	MCF-7	breast:
15	chr1:8085963..8086612-chr3:113464628..113465479,2	HCT-116	colon:
16	chr3:113440653..113444189-chr3:113444738..113447861,4	K562	blood:
17	chr3:113415208..113417503-chr3:113452735..113455867,4	K562	blood:
18	chr3:113446389..113448744-chr3:113460287..113462376,2	K562	blood:
19	chr3:113430803..113433156-chr3:113465877..113467760,2	K562	blood:
20	chr3:113454439..113456522-chr3:113456826..113458357,2	MCF-7	breast:
21	chr3:113413854..113415987-chr3:113438582..113440187,2	MCF-7	breast:
22	chr3:113456365..113458502-chr3:113458726..113460409,2	MCF-7	breast:
23	chr3:113440653..113444189-chr3:113445171..113447861,3	K562	blood:
24	chr3:113446389..113448744-chr3:113460287..113462376,2	K562	blood:
25	chr3:113464701..113467422-chr3:113608653..113611479,2	K562	blood:
26	chr3:113437875..113440758-chr3:113442135..113445039,2	MCF-7	breast:
27	chr3:113371641..113374118-chr3:113442393..113444136,2	K562	blood:
28	chr3:113465766..113466525-chr7:1498681..1499193,2	Hela-S3	cervix:
29	chr3:113435155..113437816-chr3:113460130..113462282,2	K562	blood:
30	chr3:113467223..113469542-chr3:113505191..113506704,2	K562	blood:
31	chr3:113467830..113469667-chr3:113473672..113475513,2	MCF-7	breast:
32	chr3:113445084..113447800-chr3:113453613..113455367,2	MCF-7	breast:
33	chr2:151983352..151983852-chr3:113433304..113434297,2	NB4	blood:
34	chr3:113232788..113235774-chr3:113464780..113467765,2	MCF-7	breast:
35	chr3:113415334..113416894-chr3:113456404..113458988,2	K562	blood:
36	chr3:113442105..113445216-chr3:113449989..113452556,3	MCF-7	breast:
37	chr3:113427379..113429367-chr3:113435162..113437833,2	K562	blood:
38	chr3:113414100..113416894-chr3:113456404..113459311,4	K562	blood:
39	chr3:113425527..113427592-chr3:113438461..113440250,2	K562	blood:
40	chr3:113425527..113427592-chr3:113438461..113440250,2	K562	blood:
41	chr3:113429509..113431223-chr3:113434252..113436219,2	MCF-7	breast:
42	chr3:113233753..113235613-chr3:113463995..113467002,3	MCF-7	breast:
43	chr3:113456365..113458502-chr3:113458726..113460409,2	MCF-7	breast:
44	chr3:113427683..113431366-chr3:113462294..113467024,4	MCF-7	breast:
45	chr3:113441202..113443932-chr3:113464494..113467019,3	MCF-7	breast:
46	chr3:113448745..113451424-chr3:113457105..113459746,2	K562	blood:
47	chr3:113442105..113445216-chr3:113449989..113452556,3	MCF-7	breast:
48	chr3:113453891..113455745-chr3:113519659..113522484,2	K562	blood:
49	chr19:49141193..49142091-chr3:113464774..113465547,2	NB4	blood:
50	chr3:113435155..113437816-chr3:113460130..113462282,2	K562	blood:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NAA50-2	chr3:113432278-113432405	XLOC_003221
2	lnc-NAA50-1	chr3:113466213-113466255	ENSG00000242659
3	lnc-NAA50-1	chr3:113465719-113465978	ENSG00000242659
4	lnc-NAA50-2	chr3:113432476-113433137	XLOC_003221
5	lnc-KIAA2018-2	chr3:113459670-113460101	NONHSAT091243

No data

(count:5 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	NAA50	hsa-miR-155-5p	chr3:113439890-113439884
2	NAA50	hsa-miR-192-5p	chr3:113439712-113439730
3	NAA50	hsa-miR-215-5p	chr3:113439712-113439730
4	NAA50	hsa-miR-192-5p	chr3:113439718-113439712
5	NAA50	hsa-miR-215-5p	chr3:113439718-113439712

Variant related genes	Relation type
ENSG00000242659	TF binding region
ATP6V1A	TF binding region
NAA50	TF binding region
ENSG00000239280	TF binding region
ENSG00000242659	CpG island
ATP6V1A	CpG island
NAA50	CpG island
ENSG00000239280	CpG island
ENSG00000178075	chromatin interactions
ENSG00000232871	chromatin interactions
ENSG00000145907	chromatin interactions
ENSG00000163611	chromatin interactions
ENSG00000242659	chromatin interactions
ENSG00000116285	chromatin interactions
ENSG00000155508	chromatin interactions
ENSG00000102606	chromatin interactions
ENSG00000239280	chromatin interactions
ENSG00000072858	chromatin interactions
ENSG00000121579	chromatin interactions
ENSG00000163507	chromatin interactions
ENSG00000063180	chromatin interactions
ENSG00000114573	chromatin interactions
ENSG00000240661	chromatin interactions
ENSG00000163428	chromatin interactions
ENSG00000176542	chromatin interactions
ENSG00000198919	chromatin interactions
ENSG00000164877	chromatin interactions

Extended variants
information (count: 1487 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:1487 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs144213673	chr3:113426285-113426286	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs534098024	chr3:113426294-113426295	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs567435265	chr3:113426305-113426306	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs551980081	chr3:113426369-113426370	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs13085192	chr3:113426374-113426375	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs555946264	chr3:113426392-113426393	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs577174355	chr3:113426405-113426406	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs537814000	chr3:113426456-113426457	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs141301474	chr3:113426496-113426497	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs574831104	chr3:113426512-113426513	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs370897447	chr3:113426513-113426514	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs560295737	chr3:113426532-113426533	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs150206288	chr3:113426573-113426574	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs138800417	chr3:113426590-113426591	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs60887937	chr3:113426659-113426660	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs192539363	chr3:113426753-113426754	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs532142655	chr3:113426762-113426763	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs149095847	chr3:113426763-113426764	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs143121085	chr3:113426849-113426850	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs529739421	chr3:113426925-113426926	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs534379679	chr3:113426953-113426954	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs138953448	chr3:113426957-113426958	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs183970087	chr3:113426962-113426963	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs370318668	chr3:113426965-113426966	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs552512494	chr3:113426971-113426972	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs570644194	chr3:113426973-113426974	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs371374748	chr3:113426998-113426999	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs142859300	chr3:113427002-113427003	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs556260241	chr3:113427060-113427061	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs374271501	chr3:113427122-113427123	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs147355611	chr3:113427145-113427146	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs544966434	chr3:113427276-113427277	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs188918939	chr3:113427290-113427291	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs572308551	chr3:113427311-113427312	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs545949752	chr3:113427325-113427326	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs564846582	chr3:113427366-113427367	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs576641235	chr3:113427372-113427373	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs137861125	chr3:113427510-113427511	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs377344964	chr3:113427513-113427514	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs558576920	chr3:113427516-113427517	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs562361078	chr3:113427520-113427521	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs563970064	chr3:113427527-113427528	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs75743133	chr3:113427532-113427533	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs552845423	chr3:113427546-113427547	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs3732794	chr3:113427570-113427571	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs560251710	chr3:113427579-113427580	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs527526691	chr3:113427608-113427609	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs552394995	chr3:113427614-113427615	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs193073708	chr3:113427655-113427656	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs531489061	chr3:113427711-113427712	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:59)

Disease	PMID	Source
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	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
Breast cancer	16608533	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Developmental delay	22180640	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Multiple myeloma	17550852	CNVD
small cell lung cancer	20016488	CNVD
Basal cell lymphoma	21115979	CNVD
Attention deficit hyperactivity disorder	22180640	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Ovarian cancer	22174824	CNVD
Ductal carcinoma	22052326	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:1681 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:113418200-113436800	Weak transcription	Pancreas	Pancrea
2	chr3:113418200-113436800	Weak transcription	Psoas Muscle	Psoas
3	chr3:113425000-113430400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr3:113430400-113432200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr3:113430600-113434200	Weak transcription	HUVEC	blood vessel
6	chr3:113430800-113432200	Enhancers	A549	lung
7	chr3:113431000-113431200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr3:113431000-113431400	Enhancers	Brain Hippocampus Middle	brain
9	chr3:113431000-113431400	Enhancers	K562	blood
10	chr3:113431000-113431600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr3:113431000-113432200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr3:113431000-113432200	Enhancers	HMEC	breast
13	chr3:113431200-113431400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr3:113431200-113431400	Enhancers	Brain Inferior Temporal Lobe	brain
15	chr3:113431200-113431400	Enhancers	GM12878-XiMat	blood
16	chr3:113431200-113436800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr3:113431400-113431600	Enhancers	Primary hematopoietic stem cells short term culture	blood
18	chr3:113431400-113431600	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
19	chr3:113431400-113431600	Enhancers	Brain Substantia Nigra	brain
20	chr3:113431400-113431600	Enhancers	NHEK	skin
21	chr3:113431400-113433600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr3:113431400-113436600	Weak transcription	Brain Inferior Temporal Lobe	brain
23	chr3:113431400-113436800	Weak transcription	HUES6 Cell Line	embryonic stem cell
24	chr3:113431400-113436800	Weak transcription	GM12878-XiMat	blood
25	chr3:113431400-113439400	Weak transcription	Brain Hippocampus Middle	brain
26	chr3:113431400-113439400	Weak transcription	K562	blood
27	chr3:113431600-113434000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
28	chr3:113431600-113435000	Weak transcription	Monocytes-CD14+_RO01746	blood
29	chr3:113431600-113436600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
30	chr3:113431600-113436800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr3:113431600-113437000	Weak transcription	NHEK	skin
32	chr3:113431600-113439600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
33	chr3:113431600-113443600	Weak transcription	Brain Substantia Nigra	brain
34	chr3:113431800-113432000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
35	chr3:113431800-113433800	Weak transcription	Muscle Satellite Cultured Cells	--
36	chr3:113431800-113438800	Weak transcription	Primary T cells fromperipheralblood	blood
37	chr3:113432000-113432200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
38	chr3:113432000-113432200	Enhancers	Skeletal Muscle Male	skeletal muscle
39	chr3:113432000-113436000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
40	chr3:113432000-113436800	Weak transcription	Primary B cells from cord blood	blood
41	chr3:113432000-113436800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
42	chr3:113432000-113439600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
43	chr3:113432200-113432400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
44	chr3:113432200-113433600	Weak transcription	A549	lung
45	chr3:113432200-113434200	Weak transcription	HMEC	breast
46	chr3:113432200-113434400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
47	chr3:113432200-113435200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
48	chr3:113432200-113436600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
49	chr3:113432200-113436600	Weak transcription	Fetal Muscle Leg	muscle
50	chr3:113432200-113439400	Weak transcription	Skeletal Muscle Male	skeletal muscle

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