Variant report

Variant	nsv1023578
Chromosome Location	chr7:110931210-111136259
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1560)
CpG islands
(count:184)
Chromatin interactive
region (count:169)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1560 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:111118669-111118974	K562	blood:	n/a	n/a
2	ARID3A	chr7:111116731-111117824	K562	blood:	n/a	n/a
3	ARID3A	chr7:111099362-111100398	K562	blood:	n/a	n/a
4	ARID3A	chr7:111126348-111127214	K562	blood:	n/a	n/a
5	ARID3A	chr7:111126639-111126960	HepG2	liver:	n/a	n/a
6	ARID3A	chr7:110968691-110969273	K562	blood:	n/a	n/a
7	ARID3A	chr7:110946747-110946768	K562	blood:	n/a	n/a
8	ARID3A	chr7:111100636-111100911	K562	blood:	n/a	chr7:111100841-111100857
9	ARID3A	chr7:111077670-111079453	K562	blood:	n/a	chr7:111078420-111078436 chr7:111078560-111078576
10	ARID3A	chr7:110997534-110997571	K562	blood:	n/a	n/a
11	ARID3A	chr7:111064774-111065198	HepG2	liver:	n/a	n/a
12	ARID3A	chr7:111024781-111024793	K562	blood:	n/a	n/a
13	ARID3A	chr7:110953154-110953413	K562	blood:	n/a	n/a
14	ARID3A	chr7:110969611-110970170	K562	blood:	n/a	n/a
15	ARID3A	chr7:111114444-111116392	K562	blood:	n/a	chr7:111115784-111115800 chr7:111114896-111114912 chr7:111114897-111114913
16	ARID3A	chr7:110968080-110968421	K562	blood:	n/a	n/a
17	ARID3A	chr7:110966486-110967469	K562	blood:	n/a	n/a
18	ARID3A	chr7:110967767-110967878	K562	blood:	n/a	n/a
19	ARID3A	chr7:111008626-111008764	K562	blood:	n/a	n/a
20	ARID3A	chr7:111021038-111021344	HepG2	liver:	n/a	n/a
21	ATF1	chr7:111078600-111078973	K562	blood:	n/a	n/a
22	ATF1	chr7:111054516-111054769	K562	blood:	n/a	n/a
23	ATF1	chr7:111126656-111126990	K562	blood:	n/a	n/a
24	ATF1	chr7:111012802-111012930	K562	blood:	n/a	n/a
25	ATF1	chr7:111115090-111115592	K562	blood:	n/a	n/a
26	ATF1	chr7:111116070-111116343	K562	blood:	n/a	n/a
27	ATF2	chr7:111053704-111054218	H1-hESC	embryonic stem cell:	n/a	n/a
28	ATF3	chr7:111116052-111116358	K562	blood:	n/a	n/a
29	ATF3	chr7:111078506-111078989	K562	blood:	n/a	n/a
30	BACH1	chr7:110935269-110935465	K562	blood:	n/a	n/a
31	BATF	chr7:111029015-111029334	GM12878	blood:	n/a	n/a
32	BATF	chr7:110992517-110992735	GM12878	blood:	n/a	n/a
33	BATF	chr7:110960156-110960503	GM12878	blood:	n/a	n/a
34	BCL11A	chr7:111029036-111029324	GM12878	blood:	n/a	n/a
35	BHLHE40	chr7:111126597-111126935	K562	blood:	n/a	n/a
36	BHLHE40	chr7:111134624-111134628	K562	blood:	n/a	n/a
37	BHLHE40	chr7:111078559-111079458	K562	blood:	n/a	n/a
38	BHLHE40	chr7:110964357-110964616	GM12878	blood:	n/a	n/a
39	BHLHE40	chr7:111125938-111126377	K562	blood:	n/a	n/a
40	BHLHE40	chr7:111116668-111117082	K562	blood:	n/a	n/a
41	BHLHE40	chr7:111115170-111115607	K562	blood:	n/a	n/a
42	BHLHE40	chr7:111117429-111117846	K562	blood:	n/a	n/a
43	BHLHE40	chr7:111114414-111114577	K562	blood:	n/a	n/a
44	CBX3	chr7:110983037-110983415	K562	blood:	n/a	n/a
45	CBX3	chr7:110983007-110983449	K562	blood:	n/a	n/a
46	CBX3	chr7:111078458-111079603	K562	blood:	n/a	n/a
47	CBX3	chr7:111115072-111115643	K562	blood:	n/a	n/a
48	CBX3	chr7:111051022-111051426	K562	blood:	n/a	n/a
49	CBX3	chr7:111076674-111077685	K562	blood:	n/a	n/a
50	CBX3	chr7:111079900-111081343	K562	blood:	n/a	n/a

(count:184 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:111079100-111079150	GM12891	blood:	n/a
2	chr7:111079100-111079150	GM12891	blood:	n/a
3	chr7:111079100-111079150	PrEC	prostate:	n/a
4	chr7:111086055-111086105	HCT-116	colon:	n/a
5	chr7:111079100-111079150	GM19239	blood:	n/a
6	chr7:111033064-111033114	HNPCEpiC	eye:	n/a
7	chr7:111033064-111033114	GM19239	blood:	n/a
8	chr7:111086055-111086105	T-47D	breast:	n/a
9	chr7:111033064-111033114	HAEpiC	amniotic membrane:	n/a
10	chr7:111079100-111079150	HCT-116	colon:	n/a
11	chr7:111086055-111086105	HRPEpiC	eye:	n/a
12	chr7:111033064-111033114	H1-hESC	embryonic stem cell:	embryo
13	chr7:111033064-111033114	Hela-S3	cervix:	n/a
14	chr7:111079100-111079150	HRPEpiC	eye:	n/a
15	chr7:111086055-111086105	H1-hESC	embryonic stem cell:	embryo
16	chr7:111079100-111079150	BE2_C	brain:	n/a
17	chr7:111033064-111033114	NT2-D1	testis:	n/a
18	chr7:111079100-111079150	HAEpiC	amniotic membrane:	n/a
19	chr7:111033064-111033114	HCT-116	colon:	n/a
20	chr7:111086055-111086105	HRCEpiC	kidney:	n/a
21	chr7:111086055-111086105	SK-N-SH	brain:	n/a
22	chr7:111086055-111086105	IMR90	lung:	fetal
23	chr7:111086055-111086105	CMK	blood:	n/a
24	chr7:111033064-111033114	ECC-1	luminal epithelium:	n/a
25	chr7:111033064-111033114	HEEpiC	esophagus:	n/a
26	chr7:111079100-111079150	LNCaP	prostate:	n/a
27	chr7:111033064-111033114	HPAEpiC	pulmonary alveolar:	n/a
28	chr7:111086055-111086105	A549	lung:	n/a
29	chr7:111086055-111086105	NT2-D1	testis:	n/a
30	chr7:111033064-111033114	SKMC	muscle:	n/a
31	chr7:111033064-111033114	HUVEC	blood vessel:	n/a
32	chr7:111033064-111033114	K562	blood:	n/a
33	chr7:111086055-111086105	NHDF-neo	bronchial:	n/a
34	chr7:111033064-111033114	AG04449	skin:	fetal
35	chr7:111033064-111033114	AG09309	skin:	n/a
36	chr7:111086055-111086105	ProgFib	skin:	n/a
37	chr7:111033064-111033114	HRE	kidney:	n/a
38	chr7:111079100-111079150	HUVEC	blood vessel:	n/a
39	chr7:111033064-111033114	HIPEpiC	eye:	n/a
40	chr7:111079100-111079150	HCM	heart:	n/a
41	chr7:111086055-111086105	U87	brain:	n/a
42	chr7:111033064-111033114	A549	lung:	n/a
43	chr7:111079100-111079150	NT2-D1	testis:	n/a
44	chr7:111079100-111079150	HCF	heart:	n/a
45	chr7:111086055-111086105	HNPCEpiC	eye:	n/a
46	chr7:111033064-111033114	GM06990	blood:	n/a
47	chr7:111079100-111079150	IMR90	lung:	fetal
48	chr7:111033064-111033114	PANC-1	pancreas:	n/a
49	chr7:111033064-111033114	ovcar-3	ovarian:	n/a
50	chr7:111079100-111079150	HL-60	blood:	n/a

(count:169 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type
1	chr7:110969454..110970228-chr7:111375556..111376647,3	MCF-7	breast:
2	chr7:110946449..110947994-chr7:110949688..110952187,2	K562	blood:
3	chr7:110968689..110972135-chr7:110972915..110976641,3	K562	blood:
4	chr7:110730162..110730849-chr7:111126372..111127229,2	MCF-7	breast:
5	chr7:110729634..110730189-chr7:110952732..110953606,2	MCF-7	breast:
6	chr7:110941905..110944454-chr7:110944620..110946786,2	K562	blood:
7	chr7:111103589..111105456-chr7:111112763..111114661,2	K562	blood:
8	chr7:111003207..111005251-chr7:111008050..111010228,2	K562	blood:
9	chr7:111067248..111069567-chr7:111070405..111074153,3	K562	blood:
10	chr5:125812513..125813255-chr7:110998210..110998982,2	MCF-7	breast:
11	chr7:110959334..110960882-chr7:110965813..110967484,2	K562	blood:
12	chr7:111078917..111081356-chr7:111081507..111085373,3	K562	blood:
13	chr7:111099286..111101229-chr7:111113848..111115387,2	K562	blood:
14	chr7:110729473..110730895-chr7:111126285..111127252,5	MCF-7	breast:
15	chr7:111079252..111081356-chr7:111081507..111084110,2	K562	blood:
16	chr7:110985007..110987369-chr7:110994363..110996141,2	K562	blood:
17	chr7:110934094..110935861-chr7:110939196..110941083,3	K562	blood:
18	chr7:111014312..111015875-chr7:111016018..111018954,2	MCF-7	breast:
19	chr7:111033110..111035570-chr7:111037254..111039437,2	K562	blood:
20	chr7:110973996..110977417-chr7:110978130..110980823,3	K562	blood:
21	chr7:111017537..111020347-chr7:111082285..111084321,2	K562	blood:
22	chr7:110964713..110967341-chr7:110967524..110969143,2	K562	blood:
23	chr7:110958175..110961174-chr7:110967524..110969443,2	K562	blood:
24	chr7:110983062..110985792-chr7:110987528..110989399,4	K562	blood:
25	chr7:111013152..111016122-chr7:111032306..111034572,2	K562	blood:
26	chr7:111092714..111094433-chr7:111113503..111115872,2	K562	blood:
27	chr7:110946449..110947994-chr7:110949688..110952187,2	K562	blood:
28	chr7:111099286..111101229-chr7:111113848..111115387,2	K562	blood:
29	chr7:111012849..111014530-chr7:111019458..111021313,2	K562	blood:
30	chr7:110959106..110960834-chr7:110964696..110967313,2	K562	blood:
31	chr7:110975357..110976070-chr7:111125914..111126817,2	K562	blood:
32	chr7:111114124..111115929-chr7:111199099..111201690,2	K562	blood:
33	chr7:110962569..110964668-chr7:110968085..110971412,3	K562	blood:
34	chr7:110958175..110961174-chr7:110967524..110969443,2	K562	blood:
35	chr7:110975243..110978153-chr7:110979724..110981495,2	K562	blood:
36	chr7:111123279..111126052-chr7:111128693..111130965,2	K562	blood:
37	chr7:111078917..111081356-chr7:111081507..111085373,3	K562	blood:
38	chr7:110969600..110972534-chr7:111078171..111081389,3	K562	blood:
39	chr7:111001961..111006807-chr7:111013802..111016795,4	K562	blood:
40	chr7:110929795..110932437-chr7:110933207..110936083,3	K562	blood:
41	chr7:111132543..111134860-chr7:111136175..111139021,3	K562	blood:
42	chr7:111106169..111107981-chr7:111111126..111114092,2	K562	blood:
43	chr7:111018295..111020688-chr7:111021531..111024788,3	MCF-7	breast:
44	chr7:111020866..111024340-chr7:111025481..111028509,4	MCF-7	breast:
45	chr7:111043409..111046006-chr7:111053282..111056029,3	K562	blood:
46	chr7:110919663..110921773-chr7:111080756..111083394,2	K562	blood:
47	chr7:110985007..110987369-chr7:110994363..110996141,2	K562	blood:
48	chr7:111111427..111114620-chr7:111124257..111128153,3	K562	blood:
49	chr7:110963413..110966213-chr7:110967085..110969024,2	K562	blood:
50	chr7:111134814..111136903-chr7:111375803..111377811,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000227948	TF binding region
IMMP2L	TF binding region
ENSG00000243621	TF binding region
ENSG00000227948	CpG island
IMMP2L	CpG island
ENSG00000243621	CpG island
ENSG00000188825	chromatin interactions
ENSG00000173114	chromatin interactions
ENSG00000243621	chromatin interactions
ENSG00000227948	chromatin interactions
ENSG00000184903	chromatin interactions

Extended variants
information (count: 6938 )
Associated
traits (count: 93 )

Variant overlapped rSNPs/rCNVs (count:6938 , 50 per page) page: 1 2 3 4 5 6 7 ... 139

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs75678276	chr7:110931227-110931228	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs190613614	chr7:110931229-110931230	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs574958074	chr7:110931277-110931278	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs539020423	chr7:110931320-110931321	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs147847461	chr7:110931393-110931394	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs560381978	chr7:110931408-110931409	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs181204300	chr7:110931422-110931423	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs539797478	chr7:110931449-110931450	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs37757	chr7:110931475-110931476	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
10	rs532052057	chr7:110931546-110931547	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs185345054	chr7:110931562-110931563	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs538453802	chr7:110931660-110931661	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs556365218	chr7:110931710-110931711	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs76383973	chr7:110931734-110931735	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs141487844	chr7:110931758-110931759	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs113805421	chr7:110931765-110931766	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs548098392	chr7:110931769-110931770	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs566742499	chr7:110931770-110931771	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs190548748	chr7:110931832-110931833	Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs372430476	chr7:110931850-110931851	Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs146979760	chr7:110931909-110931910	Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs148038643	chr7:110931914-110931915	Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs140762426	chr7:110931972-110931973	Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs4141126	chr7:110931978-110931979	Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs73422079	chr7:110931994-110931995	Flanking Active TSS Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs377745223	chr7:110932059-110932060	Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs542383856	chr7:110932061-110932062	Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs553949577	chr7:110932073-110932074	Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs572365268	chr7:110932114-110932115	Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs60535353	chr7:110932143-110932144	Flanking Active TSS Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs564487571	chr7:110932176-110932177	Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs562317215	chr7:110932177-110932178	Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs572413993	chr7:110932190-110932191	Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs138360740	chr7:110932209-110932210	Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs543902679	chr7:110932258-110932259	Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs562568049	chr7:110932259-110932260	Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs529773062	chr7:110932281-110932282	Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs541569710	chr7:110932305-110932306	Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs548356457	chr7:110932309-110932310	Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs141523717	chr7:110932410-110932411	Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs77162168	chr7:110932426-110932427	Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs552480092	chr7:110932448-110932449	Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs369396908	chr7:110932536-110932537	Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs570692705	chr7:110932610-110932611	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs10240810	chr7:110932630-110932631	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs564428572	chr7:110932649-110932650	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs1541472	chr7:110932739-110932740	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
48	rs373661858	chr7:110932760-110932761	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs37758	chr7:110932826-110932827	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs535586795	chr7:110932860-110932861	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:93)

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
Breast cancer	21509527	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
Autism	20685689	CNVD

Chromatin state (count:804 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:110929800-110931600	Enhancers	HSMMtube	muscle
2	chr7:110930400-110931400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
3	chr7:110930600-110931400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr7:110930600-110931400	Enhancers	Duodenum Smooth Muscle	Duodenum
5	chr7:110930600-110931400	Enhancers	Psoas Muscle	Psoas
6	chr7:110930600-110932800	Enhancers	Adipose Nuclei	Adipose
7	chr7:110931000-110931800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
8	chr7:110931000-110931800	Enhancers	Colon Smooth Muscle	Colon
9	chr7:110931000-110933200	Enhancers	Brain Germinal Matrix	brain
10	chr7:110931200-110932000	Weak transcription	Fetal Lung	lung
11	chr7:110931200-110932800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
12	chr7:110931200-110932800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
13	chr7:110931400-110932800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
14	chr7:110931400-110938200	Weak transcription	Psoas Muscle	Psoas
15	chr7:110931600-110932400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr7:110931600-110932600	Enhancers	Pancreatic Islets	Pancreatic Islet
17	chr7:110931800-110932200	Weak transcription	Colon Smooth Muscle	Colon
18	chr7:110931800-110932600	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr7:110932000-110932200	Enhancers	Fetal Lung	lung
20	chr7:110932000-110932600	Enhancers	Muscle Satellite Cultured Cells	--
21	chr7:110932000-110932600	Enhancers	Osteobl	bone
22	chr7:110932000-110932800	Enhancers	Breast Myoepithelial Primary Cells	Breast
23	chr7:110932200-110932800	Enhancers	Cortex derived primary cultured neurospheres	brain
24	chr7:110932200-110932800	Enhancers	Colon Smooth Muscle	Colon
25	chr7:110932400-110932600	Enhancers	Skeletal Muscle Female	skeletal muscle
26	chr7:110932600-110936400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
27	chr7:110932800-110936800	Weak transcription	Adipose Nuclei	Adipose
28	chr7:110933000-110938200	Weak transcription	Skeletal Muscle Female	skeletal muscle
29	chr7:110935200-110935600	Enhancers	K562	blood
30	chr7:110935400-110935600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
31	chr7:110936400-110938200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr7:110936800-110938400	Enhancers	Adipose Nuclei	Adipose
33	chr7:110938200-110938800	Enhancers	Psoas Muscle	Psoas
34	chr7:110938200-110939400	Enhancers	Skeletal Muscle Female	skeletal muscle
35	chr7:110938200-110940400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
36	chr7:110939000-110939400	Enhancers	Skeletal Muscle Male	skeletal muscle
37	chr7:110943600-110945400	Enhancers	Dnd41	blood
38	chr7:110945000-110945400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
39	chr7:110951400-110952200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
40	chr7:110952800-110954200	Enhancers	K562	blood
41	chr7:110953000-110953200	Enhancers	Primary hematopoietic stem cells	blood
42	chr7:110953000-110953400	Enhancers	Fetal Thymus	thymus
43	chr7:110953000-110953400	Enhancers	Psoas Muscle	Psoas
44	chr7:110953000-110954000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
45	chr7:110953200-110953600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
46	chr7:110953200-110954000	Enhancers	Dnd41	blood
47	chr7:110953200-110955200	Weak transcription	Primary hematopoietic stem cells	blood
48	chr7:110953600-110953800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
49	chr7:110953800-110954200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
50	chr7:110954000-110955200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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