Variant report

Variant	nsv1019591
Chromosome Location	chr7:110918701-111233418
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3092)
CpG islands
(count:977)
Chromatin interactive
region (count:279)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:3092 , 50 per page) page: 1 2 3 4 5 6 7 ... 62

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:111008626-111008764	K562	blood:	n/a	n/a
2	ARID3A	chr7:110968080-110968421	K562	blood:	n/a	n/a
3	ARID3A	chr7:110967767-110967878	K562	blood:	n/a	n/a
4	ARID3A	chr7:110997534-110997571	K562	blood:	n/a	n/a
5	ARID3A	chr7:110969611-110970170	K562	blood:	n/a	n/a
6	ARID3A	chr7:111126639-111126960	HepG2	liver:	n/a	n/a
7	ARID3A	chr7:111114444-111116392	K562	blood:	n/a	chr7:111115784-111115800 chr7:111114896-111114912 chr7:111114897-111114913
8	ARID3A	chr7:111021038-111021344	HepG2	liver:	n/a	n/a
9	ARID3A	chr7:110953154-110953413	K562	blood:	n/a	n/a
10	ARID3A	chr7:111181171-111181430	HepG2	liver:	n/a	n/a
11	ARID3A	chr7:111077670-111079453	K562	blood:	n/a	chr7:111078420-111078436 chr7:111078560-111078576
12	ARID3A	chr7:111064774-111065198	HepG2	liver:	n/a	n/a
13	ARID3A	chr7:110968691-110969273	K562	blood:	n/a	n/a
14	ARID3A	chr7:111099362-111100398	K562	blood:	n/a	n/a
15	ARID3A	chr7:111150377-111150555	K562	blood:	n/a	n/a
16	ARID3A	chr7:111170171-111170509	HepG2	liver:	n/a	n/a
17	ARID3A	chr7:110966486-110967469	K562	blood:	n/a	n/a
18	ARID3A	chr7:111024781-111024793	K562	blood:	n/a	n/a
19	ARID3A	chr7:111172220-111172476	K562	blood:	n/a	n/a
20	ARID3A	chr7:111116731-111117824	K562	blood:	n/a	n/a
21	ARID3A	chr7:110946747-110946768	K562	blood:	n/a	n/a
22	ARID3A	chr7:111202247-111202264	HepG2	liver:	n/a	n/a
23	ARID3A	chr7:111126348-111127214	K562	blood:	n/a	n/a
24	ARID3A	chr7:111202492-111202797	HepG2	liver:	n/a	n/a
25	ARID3A	chr7:111100636-111100911	K562	blood:	n/a	chr7:111100841-111100857
26	ARID3A	chr7:111199925-111200215	K562	blood:	n/a	n/a
27	ARID3A	chr7:111157885-111158000	HepG2	liver:	n/a	n/a
28	ARID3A	chr7:111202485-111202878	K562	blood:	n/a	n/a
29	ARID3A	chr7:111118669-111118974	K562	blood:	n/a	n/a
30	ATF1	chr7:111116070-111116343	K562	blood:	n/a	n/a
31	ATF1	chr7:111139180-111139448	K562	blood:	n/a	n/a
32	ATF1	chr7:111078600-111078973	K562	blood:	n/a	n/a
33	ATF1	chr7:111054516-111054769	K562	blood:	n/a	n/a
34	ATF1	chr7:111012802-111012930	K562	blood:	n/a	n/a
35	ATF1	chr7:111163232-111163327	K562	blood:	n/a	n/a
36	ATF1	chr7:111172136-111172453	K562	blood:	n/a	n/a
37	ATF1	chr7:111115090-111115592	K562	blood:	n/a	n/a
38	ATF1	chr7:111126656-111126990	K562	blood:	n/a	n/a
39	ATF1	chr7:111175451-111175458	K562	blood:	n/a	n/a
40	ATF2	chr7:111167450-111168045	GM12878	blood:	n/a	n/a
41	ATF2	chr7:111053704-111054218	H1-hESC	embryonic stem cell:	n/a	n/a
42	ATF2	chr7:111201787-111202190	H1-hESC	embryonic stem cell:	n/a	n/a
43	ATF2	chr7:111167522-111167997	GM12878	blood:	n/a	n/a
44	ATF3	chr7:111138942-111139670	A549	lung:	n/a	n/a
45	ATF3	chr7:111201918-111202678	K562	blood:	n/a	n/a
46	ATF3	chr7:111116052-111116358	K562	blood:	n/a	n/a
47	ATF3	chr7:111156585-111157142	A549	lung:	n/a	chr7:111156907-111156914 chr7:111156904-111156914 chr7:111156906-111156917 chr7:111156906-111156920 chr7:111156904-111156917 chr7:111156904-111156915
48	ATF3	chr7:111078506-111078989	K562	blood:	n/a	n/a
49	ATF3	chr7:111156586-111157138	A549	lung:	n/a	chr7:111156907-111156914 chr7:111156904-111156914 chr7:111156906-111156917 chr7:111156906-111156920 chr7:111156904-111156917 chr7:111156904-111156915
50	ATF3	chr7:111138963-111139597	A549	lung:	n/a	n/a

(count:977 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:111202450-111202500	HAEpiC	amniotic membrane:	n/a
2	chr7:111202450-111202500	HAEpiC	amniotic membrane:	n/a
3	chr7:111202666-111202716	HCT-116	colon:	n/a
4	chr7:111202395-111202445	AoSMC	blood vessel:	n/a
5	chr7:111079100-111079150	HCT-116	colon:	n/a
6	chr7:111198163-111198213	T-47D	breast:	n/a
7	chr7:111200944-111200994	HAEpiC	amniotic membrane:	n/a
8	chr7:111198163-111198213	ProgFib	skin:	n/a
9	chr7:111203008-111203058	AG09319	gingival:	n/a
10	chr7:111202682-111202732	IMR90	lung:	fetal
11	chr7:111202395-111202445	LNCaP	prostate:	n/a
12	chr7:111202666-111202716	ProgFib	skin:	n/a
13	chr7:111198163-111198213	SK-N-SH	brain:	n/a
14	chr7:111202755-111202805	AG09319	gingival:	n/a
15	chr7:111086055-111086105	AG09319	gingival:	n/a
16	chr7:111086055-111086105	GM06990	blood:	n/a
17	chr7:111200944-111200994	NHBE	bronchial:	n/a
18	chr7:111200944-111200994	ProgFib	skin:	n/a
19	chr7:111200944-111200994	HEEpiC	esophagus:	n/a
20	chr7:111086055-111086105	HRE	kidney:	n/a
21	chr7:111202755-111202805	NB4	blood:	n/a
22	chr7:111198163-111198213	AG09319	gingival:	n/a
23	chr7:111202450-111202500	ECC-1	luminal epithelium:	n/a
24	chr7:111200944-111200994	HRCEpiC	kidney:	n/a
25	chr7:111202755-111202805	AG09309	skin:	n/a
26	chr7:111204826-111204876	ovcar-3	ovarian:	n/a
27	chr7:111079100-111079150	GM19239	blood:	n/a
28	chr7:111202679-111202729	HIPEpiC	eye:	n/a
29	chr7:111202457-111202507	GM12891	blood:	n/a
30	chr7:111079100-111079150	T-47D	breast:	n/a
31	chr7:111203008-111203058	GM12891	blood:	n/a
32	chr7:111202682-111202732	AG10803	skin:	n/a
33	chr7:111079100-111079150	SK-N-SH	brain:	n/a
34	chr7:111204826-111204876	HCT-116	colon:	n/a
35	chr7:111202450-111202500	H1-hESC	embryonic stem cell:	embryo
36	chr7:111079100-111079150	HCPEpiC	choroid plexus:	n/a
37	chr7:111202682-111202732	ProgFib	skin:	n/a
38	chr7:111079100-111079150	ProgFib	skin:	n/a
39	chr7:111204826-111204876	Hepatocyte	liver:	n/a
40	chr7:111202682-111202732	K562	blood:	n/a
41	chr7:111079100-111079150	U87	brain:	n/a
42	chr7:111204826-111204876	IMR90	lung:	fetal
43	chr7:111198163-111198213	HPAEpiC	pulmonary alveolar:	n/a
44	chr7:111086055-111086105	Caco-2	colon:	n/a
45	chr7:111203008-111203058	SK-N-SH	brain:	n/a
46	chr7:111204826-111204876	AG09309	skin:	n/a
47	chr7:111200944-111200994	A549	lung:	n/a
48	chr7:111202679-111202729	MCF10A-Er-Src	breast:	n/a
49	chr7:111033064-111033114	NB4	blood:	n/a
50	chr7:111200944-111200994	HUVEC	blood vessel:	n/a

(count:279 , 50 per page) page: 1 2 3 4 5 6

No.	Distal block	Cell Line	Cell type
1	chr7:111020866..111024340-chr7:111025481..111028509,4	MCF-7	breast:
2	chr7:110946954..110949529-chr7:111129446..111130953,2	MCF-7	breast:
3	chr7:110955341..110956918-chr7:110957234..110959729,2	K562	blood:
4	chr7:111199186..111200731-chr7:111244724..111246694,2	K562	blood:
5	chr7:111179597..111181133-chr7:111200922..111203708,2	K562	blood:
6	chr7:110970635..110973843-chr7:110975141..110978905,5	K562	blood:
7	chr19:16738439..16739222-chr7:111202426..111202989,2	HCT-116	colon:
8	chr7:110969600..110972534-chr7:111078171..111081389,3	K562	blood:
9	chr7:110958175..110962470-chr7:110967524..110970471,4	K562	blood:
10	chr7:111150770..111153588-chr7:111154725..111157322,3	K562	blood:
11	chr7:111132543..111134860-chr7:111136175..111139021,3	K562	blood:
12	chr7:110729634..110730189-chr7:110952732..110953606,2	MCF-7	breast:
13	chr7:111123279..111126052-chr7:111128693..111130965,2	K562	blood:
14	chr7:111178493..111181177-chr7:111184776..111187564,2	K562	blood:
15	chr7:111078917..111081356-chr7:111081507..111085373,3	K562	blood:
16	chr7:111098758..111101723-chr7:111103712..111106818,3	K562	blood:
17	chr7:110970018..110971875-chr7:110977199..110979815,2	K562	blood:
18	chr7:110730162..110730849-chr7:111126372..111127229,2	MCF-7	breast:
19	chr7:111183053..111185306-chr7:111210487..111212870,2	K562	blood:
20	chr7:111043409..111046006-chr7:111053282..111056029,3	K562	blood:
21	chr7:111164149..111167742-chr7:111173784..111176807,4	K562	blood:
22	chr7:111178053..111179952-chr7:111201249..111203327,2	MCF-7	breast:
23	chr7:111181285..111183708-chr7:111185192..111188559,3	K562	blood:
24	chr7:111013152..111016122-chr7:111032306..111034572,2	K562	blood:
25	chr7:110935982..110938365-chr7:110942817..110944691,2	K562	blood:
26	chr7:111165046..111167501-chr7:111171827..111173680,2	K562	blood:
27	chr17:41463788..41465299-chr7:111034758..111036259,2	K562	blood:
28	chr7:111172229..111174380-chr7:111191411..111194309,2	K562	blood:
29	chr7:111079252..111081356-chr7:111081507..111084110,2	K562	blood:
30	chr7:111162292..111164581-chr7:111182567..111185234,2	K562	blood:
31	chr7:111003207..111005251-chr7:111008050..111010228,2	K562	blood:
32	chr7:111176865..111178433-chr7:111182046..111183894,2	K562	blood:
33	chr7:111018357..111021397-chr7:111023712..111026997,4	K562	blood:
34	chr7:110934094..110935861-chr7:110939196..110941083,3	K562	blood:
35	chr7:110959106..110960834-chr7:110964696..110967313,2	K562	blood:
36	chr7:111136494..111138259-chr7:111146295..111147835,2	K562	blood:
37	chr7:110994957..110999323-chr7:111001198..111006593,6	K562	blood:
38	chr7:111226200..111228452-chr7:111228554..111231372,2	K562	blood:
39	chr7:111173111..111178494-chr7:111200645..111202653,4	MCF-7	breast:
40	chr7:110953570..110955733-chr7:111376151..111377847,2	MCF-7	breast:
41	chr7:111118102..111121485-chr7:111125299..111129711,6	K562	blood:
42	chr7:110983062..110985792-chr7:110987528..110989399,4	K562	blood:
43	chr7:111160191..111162473-chr7:111166967..111168569,3	K562	blood:
44	chr7:111123279..111126052-chr7:111128693..111130965,2	K562	blood:
45	chr7:110911704..110914495-chr7:111113882..111116767,2	K562	blood:
46	chr7:110941905..110944454-chr7:110944620..110946786,2	K562	blood:
47	chr7:110994957..110999323-chr7:111001198..111006593,6	K562	blood:
48	chr7:111164979..111167158-chr7:111168899..111171034,2	MCF-7	breast:
49	chr7:111174213..111176704-chr7:111200682..111203644,3	K562	blood:
50	chr7:111154283..111157202-chr7:111157997..111159947,2	MCF-7	breast:

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
ENSG00000204444	chromatin interactions
ENSG00000178951	chromatin interactions
ENSG00000141979	chromatin interactions
ENSG00000227948	chromatin interactions
ENSG00000105085	chromatin interactions
ENSG00000204463	chromatin interactions
ENSG00000184903	chromatin interactions
ENSG00000199347	chromatin interactions
ENSG00000164327	chromatin interactions
ENSG00000173114	chromatin interactions
ENSG00000102103	chromatin interactions
ENSG00000188825	chromatin interactions
ENSG00000173409	chromatin interactions
ENSG00000243621	chromatin interactions
ENSG00000214188	chromatin interactions
ENSG00000240053	chromatin interactions
ENSG00000173812	chromatin interactions
ENSG00000126768	chromatin interactions
ENSG00000143643	chromatin interactions

Extended variants
information (count: 10501 )
Associated
traits (count: 98 )

Variant overlapped rSNPs/rCNVs (count:10501 , 50 per page) page: 1 2 3 4 5 6 7 ... 211

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs556566665	chr7:110918834-110918835	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs184249776	chr7:110918937-110918938	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs535958790	chr7:110918966-110918967	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs554302731	chr7:110918967-110918968	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs187032717	chr7:110918997-110918998	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs561767525	chr7:110919034-110919035	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs536540083	chr7:110919038-110919039	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs540469576	chr7:110919044-110919045	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs191718526	chr7:110919093-110919094	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs185361384	chr7:110919102-110919103	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs375858799	chr7:110919111-110919112	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs544597673	chr7:110919193-110919194	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs562884245	chr7:110919205-110919206	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs377501286	chr7:110919218-110919219	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs530174880	chr7:110919220-110919221	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs115471081	chr7:110919228-110919229	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs560680004	chr7:110919230-110919231	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs112039180	chr7:110919263-110919264	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs572578524	chr7:110919290-110919291	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs552771613	chr7:110919303-110919304	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs546921199	chr7:110919325-110919326	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs73201100	chr7:110919363-110919364	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs141964721	chr7:110919376-110919377	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs190212086	chr7:110919379-110919380	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs116459081	chr7:110919390-110919391	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs182170424	chr7:110919437-110919438	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs554241335	chr7:110919487-110919488	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs566605413	chr7:110919568-110919569	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs185513929	chr7:110919580-110919581	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs558747068	chr7:110919647-110919648	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs576760674	chr7:110919649-110919650	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs577037431	chr7:110919650-110919651	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs369251302	chr7:110919654-110919655	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs78015552	chr7:110919697-110919698	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs556547129	chr7:110919730-110919731	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs574879803	chr7:110919738-110919739	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs146316790	chr7:110919771-110919772	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs188240824	chr7:110919772-110919773	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs138747287	chr7:110919783-110919784	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs115093446	chr7:110919952-110919953	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs141887197	chr7:110919985-110919986	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs115541524	chr7:110920016-110920017	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs150763316	chr7:110920047-110920048	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs563958768	chr7:110920083-110920084	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs568462751	chr7:110920088-110920089	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs60204647	chr7:110920179-110920180	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs37747	chr7:110920180-110920181	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
48	rs372211875	chr7:110920209-110920210	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs180722739	chr7:110920210-110920211	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs115568858	chr7:110920212-110920213	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:98)

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
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
Autism	20685689	CNVD
Melanoma	20877625	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:2048 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:110905000-110926200	Weak transcription	Aorta	Aorta
2	chr7:110911600-110926800	Weak transcription	Primary T cells from cord blood	blood
3	chr7:110915400-110926800	Weak transcription	Ovary	ovary
4	chr7:110915800-110929800	Weak transcription	Fetal Heart	heart
5	chr7:110920400-110923400	Weak transcription	K562	blood
6	chr7:110923400-110923600	ZNF genes & repeats	K562	blood
7	chr7:110923600-110924800	Weak transcription	K562	blood
8	chr7:110924400-110931000	Weak transcription	Fetal Lung	lung
9	chr7:110926800-110927000	Enhancers	Ovary	ovary
10	chr7:110929800-110931200	Enhancers	Fetal Heart	heart
11	chr7:110929800-110931600	Enhancers	HSMMtube	muscle
12	chr7:110930400-110931400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
13	chr7:110930600-110931400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr7:110930600-110931400	Enhancers	Duodenum Smooth Muscle	Duodenum
15	chr7:110930600-110931400	Enhancers	Psoas Muscle	Psoas
16	chr7:110930600-110932800	Enhancers	Adipose Nuclei	Adipose
17	chr7:110931000-110931200	Enhancers	Fetal Lung	lung
18	chr7:110931000-110931800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr7:110931000-110931800	Enhancers	Colon Smooth Muscle	Colon
20	chr7:110931000-110933200	Enhancers	Brain Germinal Matrix	brain
21	chr7:110931200-110932000	Weak transcription	Fetal Lung	lung
22	chr7:110931200-110932800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
23	chr7:110931200-110932800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
24	chr7:110931400-110932800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
25	chr7:110931400-110938200	Weak transcription	Psoas Muscle	Psoas
26	chr7:110931600-110932400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
27	chr7:110931600-110932600	Enhancers	Pancreatic Islets	Pancreatic Islet
28	chr7:110931800-110932200	Weak transcription	Colon Smooth Muscle	Colon
29	chr7:110931800-110932600	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
30	chr7:110932000-110932200	Enhancers	Fetal Lung	lung
31	chr7:110932000-110932600	Enhancers	Muscle Satellite Cultured Cells	--
32	chr7:110932000-110932600	Enhancers	Osteobl	bone
33	chr7:110932000-110932800	Enhancers	Breast Myoepithelial Primary Cells	Breast
34	chr7:110932200-110932800	Enhancers	Cortex derived primary cultured neurospheres	brain
35	chr7:110932200-110932800	Enhancers	Colon Smooth Muscle	Colon
36	chr7:110932400-110932600	Enhancers	Skeletal Muscle Female	skeletal muscle
37	chr7:110932600-110936400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chr7:110932800-110936800	Weak transcription	Adipose Nuclei	Adipose
39	chr7:110933000-110938200	Weak transcription	Skeletal Muscle Female	skeletal muscle
40	chr7:110935200-110935600	Enhancers	K562	blood
41	chr7:110935400-110935600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
42	chr7:110936400-110938200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
43	chr7:110936800-110938400	Enhancers	Adipose Nuclei	Adipose
44	chr7:110938200-110938800	Enhancers	Psoas Muscle	Psoas
45	chr7:110938200-110939400	Enhancers	Skeletal Muscle Female	skeletal muscle
46	chr7:110938200-110940400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
47	chr7:110939000-110939400	Enhancers	Skeletal Muscle Male	skeletal muscle
48	chr7:110943600-110945400	Enhancers	Dnd41	blood
49	chr7:110945000-110945400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
50	chr7:110951400-110952200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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