Variant report

Variant	nsv1021780
Chromosome Location	chr7:110892851-111112146
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1278)
CpG islands
(count:244)
Chromatin interactive
region (count:156)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1278 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:111099362-111100398	K562	blood:	n/a	n/a
2	ARID3A	chr7:110997534-110997571	K562	blood:	n/a	n/a
3	ARID3A	chr7:110968080-110968421	K562	blood:	n/a	n/a
4	ARID3A	chr7:111008626-111008764	K562	blood:	n/a	n/a
5	ARID3A	chr7:110946747-110946768	K562	blood:	n/a	n/a
6	ARID3A	chr7:110895612-110896118	K562	blood:	n/a	n/a
7	ARID3A	chr7:110966486-110967469	K562	blood:	n/a	n/a
8	ARID3A	chr7:111064774-111065198	HepG2	liver:	n/a	n/a
9	ARID3A	chr7:111021038-111021344	HepG2	liver:	n/a	n/a
10	ARID3A	chr7:110953154-110953413	K562	blood:	n/a	n/a
11	ARID3A	chr7:111024781-111024793	K562	blood:	n/a	n/a
12	ARID3A	chr7:111077670-111079453	K562	blood:	n/a	chr7:111078420-111078436 chr7:111078560-111078576
13	ARID3A	chr7:110967767-110967878	K562	blood:	n/a	n/a
14	ARID3A	chr7:110968691-110969273	K562	blood:	n/a	n/a
15	ARID3A	chr7:110969611-110970170	K562	blood:	n/a	n/a
16	ARID3A	chr7:111100636-111100911	K562	blood:	n/a	chr7:111100841-111100857
17	ATF1	chr7:110895660-110895855	K562	blood:	n/a	n/a
18	ATF1	chr7:111012802-111012930	K562	blood:	n/a	n/a
19	ATF1	chr7:111054516-111054769	K562	blood:	n/a	n/a
20	ATF1	chr7:111078600-111078973	K562	blood:	n/a	n/a
21	ATF2	chr7:111053704-111054218	H1-hESC	embryonic stem cell:	n/a	n/a
22	ATF3	chr7:111078506-111078989	K562	blood:	n/a	n/a
23	BACH1	chr7:110935269-110935465	K562	blood:	n/a	n/a
24	BATF	chr7:111029015-111029334	GM12878	blood:	n/a	n/a
25	BATF	chr7:110992517-110992735	GM12878	blood:	n/a	n/a
26	BATF	chr7:110960156-110960503	GM12878	blood:	n/a	n/a
27	BCL11A	chr7:111029036-111029324	GM12878	blood:	n/a	n/a
28	BHLHE40	chr7:111078559-111079458	K562	blood:	n/a	n/a
29	BHLHE40	chr7:110913546-110913742	K562	blood:	n/a	n/a
30	BHLHE40	chr7:110964357-110964616	GM12878	blood:	n/a	n/a
31	CBX3	chr7:111078458-111079603	K562	blood:	n/a	n/a
32	CBX3	chr7:110969313-110970175	K562	blood:	n/a	n/a
33	CBX3	chr7:110910820-110911290	K562	blood:	n/a	n/a
34	CBX3	chr7:110983007-110983449	K562	blood:	n/a	n/a
35	CBX3	chr7:111074271-111074726	K562	blood:	n/a	n/a
36	CBX3	chr7:111090809-111091116	K562	blood:	n/a	n/a
37	CBX3	chr7:111073025-111074149	K562	blood:	n/a	n/a
38	CBX3	chr7:111051022-111051426	K562	blood:	n/a	n/a
39	CBX3	chr7:111076674-111077685	K562	blood:	n/a	n/a
40	CBX3	chr7:110983037-110983415	K562	blood:	n/a	n/a
41	CBX3	chr7:111079900-111081343	K562	blood:	n/a	n/a
42	CCNT2	chr7:110895712-110896018	K562	blood:	n/a	n/a
43	CCNT2	chr7:110896464-110896592	K562	blood:	n/a	n/a
44	CCNT2	chr7:111078445-111079337	K562	blood:	n/a	n/a
45	CCNT2	chr7:110941498-110941584	K562	blood:	n/a	n/a
46	CCNT2	chr7:110953302-110953502	K562	blood:	n/a	n/a
47	CEBPB	chr7:111077912-111078116	MCF-7	breast:	n/a	n/a
48	CEBPB	chr7:111059906-111060145	K562	blood:	n/a	n/a
49	CEBPB	chr7:110906589-110907001	A549	lung:	n/a	chr7:110906880-110906891
50	CEBPB	chr7:110900121-110900405	A549	lung:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:111079100-111079150	NHDF-neo	bronchial:	n/a
2	chr7:111079100-111079150	AG09309	skin:	n/a
3	chr7:110906785-110906835	NH-A	brain:	n/a
4	chr7:110906785-110906835	HCT-116	colon:	n/a
5	chr7:110906785-110906835	HNPCEpiC	eye:	n/a
6	chr7:111086055-111086105	HEEpiC	esophagus:	n/a
7	chr7:111086055-111086105	GM12892	blood:	n/a
8	chr7:111079100-111079150	HL-60	blood:	n/a
9	chr7:110906785-110906835	SK-N-SH	brain:	n/a
10	chr7:111033064-111033114	Hepatocyte	liver:	n/a
11	chr7:110906785-110906835	Hela-S3	cervix:	n/a
12	chr7:110906785-110906835	HEEpiC	esophagus:	n/a
13	chr7:110906785-110906835	Hepatocyte	liver:	n/a
14	chr7:111079100-111079150	HCPEpiC	choroid plexus:	n/a
15	chr7:110906785-110906835	GM12891	blood:	n/a
16	chr7:110906785-110906835	CMK	blood:	n/a
17	chr7:111033064-111033114	HCT-116	colon:	n/a
18	chr7:111079100-111079150	ovcar-3	ovarian:	n/a
19	chr7:111086055-111086105	GM06990	blood:	n/a
20	chr7:111033064-111033114	U87	brain:	n/a
21	chr7:111033064-111033114	AG10803	skin:	n/a
22	chr7:111079100-111079150	NH-A	brain:	n/a
23	chr7:111033064-111033114	GM12891	blood:	n/a
24	chr7:110906785-110906835	HMEC	breast:	n/a
25	chr7:111079100-111079150	GM12892	blood:	n/a
26	chr7:111086055-111086105	ovcar-3	ovarian:	n/a
27	chr7:111086055-111086105	NHBE	bronchial:	n/a
28	chr7:111079100-111079150	Jurkat	blood:	n/a
29	chr7:111086055-111086105	IMR90	lung:	fetal
30	chr7:111033064-111033114	NH-A	brain:	n/a
31	chr7:111033064-111033114	SK-N-SH	brain:	n/a
32	chr7:111033064-111033114	HMEC	breast:	n/a
33	chr7:111033064-111033114	PrEC	prostate:	n/a
34	chr7:111033064-111033114	PANC-1	pancreas:	n/a
35	chr7:111033064-111033114	RPTEC	kidney:	n/a
36	chr7:111079100-111079150	GM12891	blood:	n/a
37	chr7:111086055-111086105	A549	lung:	n/a
38	chr7:111086055-111086105	AG09319	gingival:	n/a
39	chr7:111086055-111086105	AG04450	lung:	fetal
40	chr7:110906785-110906835	HCF	heart:	n/a
41	chr7:111033064-111033114	HCF	heart:	n/a
42	chr7:110906785-110906835	LNCaP	prostate:	n/a
43	chr7:110906785-110906835	ProgFib	skin:	n/a
44	chr7:111086055-111086105	SK-N-MC	brain:	n/a
45	chr7:111079100-111079150	NT2-D1	testis:	n/a
46	chr7:111086055-111086105	MCF10A-Er-Src	breast:	n/a
47	chr7:111079100-111079150	PFSK-1	brain:	n/a
48	chr7:110906785-110906835	Jurkat	blood:	n/a
49	chr7:111033064-111033114	NHBE	bronchial:	n/a
50	chr7:110906785-110906835	BE2_C	brain:	n/a

(count:156 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type
1	chr7:110919285..110921892-chr7:110924129..110926222,2	K562	blood:
2	chr7:110983062..110985792-chr7:110987528..110989399,4	K562	blood:
3	chr7:111012849..111014530-chr7:111019458..111021313,2	K562	blood:
4	chr7:111020866..111024340-chr7:111025481..111028509,4	MCF-7	breast:
5	chr7:110904002..110906677-chr7:110908987..110911839,2	K562	blood:
6	chr7:111099278..111101723-chr7:111102972..111106150,5	K562	blood:
7	chr7:111103589..111105456-chr7:111112763..111114661,2	K562	blood:
8	chr7:110985007..110987369-chr7:110994363..110996141,2	K562	blood:
9	chr7:111003207..111005251-chr7:111008050..111010228,2	K562	blood:
10	chr7:111025105..111026879-chr7:111027995..111029881,2	K562	blood:
11	chr7:110975243..110978153-chr7:110979724..110981495,2	K562	blood:
12	chr7:110969852..110970371-chr7:111126745..111127278,2	K562	blood:
13	chr7:110934094..110935861-chr7:110939196..110941083,3	K562	blood:
14	chr7:110983062..110985792-chr7:110987528..110989399,4	K562	blood:
15	chr7:110959106..110960834-chr7:110964696..110967313,2	K562	blood:
16	chr7:110924808..110925532-chr7:111126328..111127072,2	MCF-7	breast:
17	chr7:110941905..110944454-chr7:110944620..110946786,2	K562	blood:
18	chr7:111033479..111035253-chr7:111039939..111041629,3	K562	blood:
19	chr7:111067141..111070112-chr7:111198227..111201087,2	K562	blood:
20	chr7:111018357..111021397-chr7:111023712..111026997,4	K562	blood:
21	chr7:110958175..110962470-chr7:110967524..110970471,4	K562	blood:
22	chr7:110977304..110981066-chr7:110982767..110987604,6	K562	blood:
23	chr7:110975243..110978153-chr7:110979724..110981495,2	K562	blood:
24	chr7:110970018..110971875-chr7:110977199..110979815,2	K562	blood:
25	chr7:110910606..110912820-chr7:110916912..110919074,2	K562	blood:
26	chr7:110935982..110938365-chr7:110942817..110944691,2	K562	blood:
27	chr7:110959106..110960834-chr7:110964696..110967313,2	K562	blood:
28	chr7:111070056..111074231-chr7:111075733..111078781,4	K562	blood:
29	chr7:110934094..110935861-chr7:110939196..110941083,3	K562	blood:
30	chr7:110946494..110948605-chr7:110949688..110952299,2	K562	blood:
31	chr7:111067248..111069567-chr7:111070405..111074153,3	K562	blood:
32	chr7:110969600..110972534-chr7:111078171..111081389,3	K562	blood:
33	chr7:110997175..111000339-chr7:111001551..111003490,3	K562	blood:
34	chr7:111070056..111074231-chr7:111075733..111078781,4	K562	blood:
35	chr7:111075731..111078683-chr7:111110429..111113130,2	K562	blood:
36	chr7:111001961..111006807-chr7:111013802..111016795,4	K562	blood:
37	chr7:110946494..110948605-chr7:110949688..110952299,2	K562	blood:
38	chr7:110959334..110960882-chr7:110965813..110967484,2	K562	blood:
39	chr7:110935982..110938365-chr7:110942817..110944691,2	K562	blood:
40	chr7:110958175..110961174-chr7:110967524..110969443,2	K562	blood:
41	chr7:110962126..110964268-chr7:110964422..110967257,2	K562	blood:
42	chr7:111075731..111078683-chr7:111110429..111113130,2	K562	blood:
43	chr17:41463788..41465299-chr7:111034758..111036259,2	K562	blood:
44	chr7:111079252..111081356-chr7:111081507..111084110,2	K562	blood:
45	chr7:111111427..111114620-chr7:111124257..111128153,3	K562	blood:
46	chr7:111043409..111046006-chr7:111053282..111056029,3	K562	blood:
47	chr7:110907955..110909675-chr7:110912861..110914751,2	K562	blood:
48	chr7:111100148..111100705-chr7:111129526..111130134,2	K562	blood:
49	chr7:110970018..110971875-chr7:110977199..110979815,2	K562	blood:
50	chr7:111096109..111097696-chr7:111100341..111102536,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DOCK4-7	chr7:110902289-110902553	expReg_chr7_8342_-

No data

Variant related genes	Relation type
ENSG00000227948	TF binding region
ENSG00000243621	TF binding region
IMMP2L	TF binding region
ENSG00000227948	CpG island
ENSG00000243621	CpG island
IMMP2L	CpG island
ENSG00000243621	chromatin interactions
ENSG00000136856	chromatin interactions
ENSG00000188825	chromatin interactions
ENSG00000227948	chromatin interactions
ENSG00000184903	chromatin interactions

Extended variants
information (count: 7469 )
Associated
traits (count: 96 )

Variant overlapped rSNPs/rCNVs (count:7469 , 50 per page) page: 1 2 3 4 5 6 7 ... 150

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1978247	chr7:110892851-110892852	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs537244899	chr7:110892862-110892863	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs527903656	chr7:110892866-110892867	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs373810886	chr7:110892878-110892879	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs367780272	chr7:110892879-110892880	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs140140461	chr7:110892887-110892888	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs112916143	chr7:110892947-110892948	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs114956267	chr7:110893069-110893070	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs145766079	chr7:110893079-110893080	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs192153399	chr7:110893161-110893162	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs567613176	chr7:110893232-110893233	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs183000386	chr7:110893241-110893242	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs547351157	chr7:110893281-110893282	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs571791929	chr7:110893297-110893298	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs80269046	chr7:110893388-110893389	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs539492130	chr7:110893391-110893392	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs371466850	chr7:110893412-110893413	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs376266379	chr7:110893429-110893430	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs148964909	chr7:110893480-110893481	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs143652687	chr7:110893509-110893510	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs537240327	chr7:110893515-110893516	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs7805473	chr7:110893560-110893561	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs573968891	chr7:110893577-110893578	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs540997245	chr7:110893584-110893585	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs532684724	chr7:110893594-110893595	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs559673534	chr7:110893635-110893636	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs577974594	chr7:110893636-110893637	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs545446755	chr7:110893650-110893651	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs141420132	chr7:110893694-110893695	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs530955436	chr7:110893732-110893733	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs549154742	chr7:110893741-110893742	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs561178128	chr7:110893769-110893770	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs528758974	chr7:110893797-110893798	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs147016321	chr7:110893805-110893806	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs570076743	chr7:110893875-110893876	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs565636075	chr7:110893890-110893891	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs539071622	chr7:110893942-110893943	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs187288460	chr7:110893944-110893945	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs569758015	chr7:110893961-110893962	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs537179422	chr7:110894002-110894003	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs555579823	chr7:110894003-110894004	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs573778781	chr7:110894034-110894035	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs192684751	chr7:110894056-110894057	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs553005049	chr7:110894074-110894075	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs577924279	chr7:110894126-110894127	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs544996258	chr7:110894177-110894178	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs551040476	chr7:110894205-110894206	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs371990782	chr7:110894242-110894243	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs143071903	chr7:110894283-110894284	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs72183788	chr7:110894284-110894285	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:96)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Melanoma	18172304	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	16864856	CNVD
Squamous cell cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	17387387	CNVD
Low-grade fibromyxoid sarcoma	0	CNVD
Oligodendroglial tumors	17285580	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21264507	CNVD
Shwachman-Diamond syndrome	22934832	CNVD
Colorectal cancer	19359472	CNVD
Cutaneous malignant melanoma	17690212	CNVD
Leukemia	17361228	CNVD
Breast cancer	16461572	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Malignant melanoma	17690212	CNVD
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Multiple myeloma	17550852	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neurodevelopmental disorder	22521361	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Metanephric adenoma	20802469	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
Myelodysplastic syndrome	21251322	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21785460	CNVD
Chronic myeloid leukemia	21384125	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	21364760	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	17053054	CNVD
Prostate cancer	16573809	CNVD
Medulloblastoma	16783165	CNVD
Melanoma	17363583	CNVD
Myelofibrosis	22110671	CNVD
Squamous cell cancer	20885788	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Breast cancer	16397240	CNVD
Biliary cancer	19435499	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Prostate cancer	23792589	CNVD
Adenocarcinoma	21044232	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Autism	19401682	CNVD
Non-small cell lung cancer	19889201	CNVD
Acute myeloid leukemia	18000384	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Metastatic melanoma	18483359	CNVD
Autism	18414403	CNVD
Autism	19546859	CNVD
Schizophrenia	19546859	CNVD
Tourette syndrome	19546859	CNVD
Melanoma	19188590	CNVD
small cell lung cancer	20016488	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Attention deficit hyperactivity disorder	19546859	CNVD
Breast cancer	21509527	CNVD
Schizophrenia	23813976	CNVD
Autism	20531469	CNVD
early-passage human iPS cells	21368824	CNVD
Pancreatic cancer	17952125	CNVD
T-cell lymphomas	22341440	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Autism	20841430	CNVD

Chromatin state (count:884 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:110882600-110903800	Weak transcription	Aorta	Aorta
2	chr7:110893400-110893600	Enhancers	iPS-15b Cell Line	embryonic stem cell
3	chr7:110893400-110893600	Enhancers	Pancreas	Pancrea
4	chr7:110893400-110893800	Enhancers	HUES6 Cell Line	embryonic stem cell
5	chr7:110893600-110894200	Enhancers	ES-I3 Cell Line	embryonic stem cell
6	chr7:110893600-110914800	Weak transcription	Pancreas	Pancrea
7	chr7:110893800-110894200	Enhancers	Cortex derived primary cultured neurospheres	brain
8	chr7:110894200-110894400	Enhancers	iPS-15b Cell Line	embryonic stem cell
9	chr7:110894200-110895800	Weak transcription	Cortex derived primary cultured neurospheres	brain
10	chr7:110894600-110895200	Enhancers	HepG2	liver
11	chr7:110895200-110896000	Enhancers	K562	blood
12	chr7:110895200-110897200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr7:110895800-110896200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr7:110895800-110896800	Enhancers	Cortex derived primary cultured neurospheres	brain
15	chr7:110895800-110896800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
16	chr7:110896000-110896400	Enhancers	Brain Hippocampus Middle	brain
17	chr7:110896200-110903600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
18	chr7:110901200-110903800	Enhancers	Osteobl	bone
19	chr7:110901200-110908200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
20	chr7:110901600-110904000	Enhancers	Pancreatic Islets	Pancreatic Islet
21	chr7:110901800-110902000	Enhancers	Muscle Satellite Cultured Cells	--
22	chr7:110901800-110902800	Enhancers	HepG2	liver
23	chr7:110902000-110902600	Weak transcription	Muscle Satellite Cultured Cells	--
24	chr7:110902400-110902800	Enhancers	A549	lung
25	chr7:110902400-110903000	Enhancers	Psoas Muscle	Psoas
26	chr7:110902600-110902800	Enhancers	Muscle Satellite Cultured Cells	--
27	chr7:110902800-110903600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
28	chr7:110902800-110905200	Weak transcription	Muscle Satellite Cultured Cells	--
29	chr7:110902800-110905800	Enhancers	Skeletal Muscle Female	skeletal muscle
30	chr7:110902800-110906600	Weak transcription	HepG2	liver
31	chr7:110902800-110912000	Weak transcription	A549	lung
32	chr7:110903000-110904600	Weak transcription	Psoas Muscle	Psoas
33	chr7:110903400-110907600	Enhancers	Fetal Lung	lung
34	chr7:110903600-110903800	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
35	chr7:110903600-110903800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
36	chr7:110903600-110904000	Enhancers	Adipose Nuclei	Adipose
37	chr7:110903600-110904800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
38	chr7:110903800-110904000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
39	chr7:110903800-110904000	Enhancers	Aorta	Aorta
40	chr7:110903800-110904600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
41	chr7:110903800-110905200	Weak transcription	Osteobl	bone
42	chr7:110903800-110906000	Enhancers	Skeletal Muscle Male	skeletal muscle
43	chr7:110903800-110908400	Enhancers	HSMMtube	muscle
44	chr7:110904000-110904200	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
45	chr7:110904000-110904400	Weak transcription	Adipose Nuclei	Adipose
46	chr7:110904000-110904400	Weak transcription	Aorta	Aorta
47	chr7:110904000-110906200	Weak transcription	Pancreatic Islets	Pancreatic Islet
48	chr7:110904200-110905000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
49	chr7:110904400-110905000	Enhancers	Aorta	Aorta
50	chr7:110904400-110905600	Enhancers	Duodenum Smooth Muscle	Duodenum

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