Variant report

Variant	nsv1019130
Chromosome Location	chr7:110835018-111266132
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3700)
CpG islands
(count:1283)
Chromatin interactive
region (count:351)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:3700 , 50 per page) page: 1 2 3 4 5 6 7 ... 74

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:110997534-110997571	K562	blood:	n/a	n/a
2	ARID3A	chr7:110969611-110970170	K562	blood:	n/a	n/a
3	ARID3A	chr7:111199925-111200215	K562	blood:	n/a	n/a
4	ARID3A	chr7:111157885-111158000	HepG2	liver:	n/a	n/a
5	ARID3A	chr7:111114444-111116392	K562	blood:	n/a	chr7:111115784-111115800 chr7:111114896-111114912 chr7:111114897-111114913
6	ARID3A	chr7:111118669-111118974	K562	blood:	n/a	n/a
7	ARID3A	chr7:111008626-111008764	K562	blood:	n/a	n/a
8	ARID3A	chr7:111099362-111100398	K562	blood:	n/a	n/a
9	ARID3A	chr7:110863537-110864343	K562	blood:	n/a	chr7:110863547-110863563 chr7:110863548-110863564
10	ARID3A	chr7:111064774-111065198	HepG2	liver:	n/a	n/a
11	ARID3A	chr7:111202247-111202264	HepG2	liver:	n/a	n/a
12	ARID3A	chr7:110953154-110953413	K562	blood:	n/a	n/a
13	ARID3A	chr7:111116731-111117824	K562	blood:	n/a	n/a
14	ARID3A	chr7:111202485-111202878	K562	blood:	n/a	n/a
15	ARID3A	chr7:111172220-111172476	K562	blood:	n/a	n/a
16	ARID3A	chr7:111202492-111202797	HepG2	liver:	n/a	n/a
17	ARID3A	chr7:111126639-111126960	HepG2	liver:	n/a	n/a
18	ARID3A	chr7:110968691-110969273	K562	blood:	n/a	n/a
19	ARID3A	chr7:110968080-110968421	K562	blood:	n/a	n/a
20	ARID3A	chr7:110946747-110946768	K562	blood:	n/a	n/a
21	ARID3A	chr7:111077670-111079453	K562	blood:	n/a	chr7:111078420-111078436 chr7:111078560-111078576
22	ARID3A	chr7:110895612-110896118	K562	blood:	n/a	n/a
23	ARID3A	chr7:111181171-111181430	HepG2	liver:	n/a	n/a
24	ARID3A	chr7:111021038-111021344	HepG2	liver:	n/a	n/a
25	ARID3A	chr7:110967767-110967878	K562	blood:	n/a	n/a
26	ARID3A	chr7:111024781-111024793	K562	blood:	n/a	n/a
27	ARID3A	chr7:111126348-111127214	K562	blood:	n/a	n/a
28	ARID3A	chr7:110966486-110967469	K562	blood:	n/a	n/a
29	ARID3A	chr7:111150377-111150555	K562	blood:	n/a	n/a
30	ARID3A	chr7:110869353-110869485	K562	blood:	n/a	n/a
31	ARID3A	chr7:111170171-111170509	HepG2	liver:	n/a	n/a
32	ARID3A	chr7:111100636-111100911	K562	blood:	n/a	chr7:111100841-111100857
33	ATF1	chr7:111115090-111115592	K562	blood:	n/a	n/a
34	ATF1	chr7:111054516-111054769	K562	blood:	n/a	n/a
35	ATF1	chr7:111078600-111078973	K562	blood:	n/a	n/a
36	ATF1	chr7:111175451-111175458	K562	blood:	n/a	n/a
37	ATF1	chr7:110863987-110864363	K562	blood:	n/a	n/a
38	ATF1	chr7:110889894-110890092	K562	blood:	n/a	n/a
39	ATF1	chr7:110895660-110895855	K562	blood:	n/a	n/a
40	ATF1	chr7:111172136-111172453	K562	blood:	n/a	n/a
41	ATF1	chr7:111012802-111012930	K562	blood:	n/a	n/a
42	ATF1	chr7:111163232-111163327	K562	blood:	n/a	n/a
43	ATF1	chr7:111126656-111126990	K562	blood:	n/a	n/a
44	ATF1	chr7:111116070-111116343	K562	blood:	n/a	n/a
45	ATF1	chr7:111139180-111139448	K562	blood:	n/a	n/a
46	ATF2	chr7:111167450-111168045	GM12878	blood:	n/a	n/a
47	ATF2	chr7:111167522-111167997	GM12878	blood:	n/a	n/a
48	ATF2	chr7:111053704-111054218	H1-hESC	embryonic stem cell:	n/a	n/a
49	ATF2	chr7:111201787-111202190	H1-hESC	embryonic stem cell:	n/a	n/a
50	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

(count:1283 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:111202450-111202500	NH-A	brain:	n/a
2	chr7:111202457-111202507	AoSMC	blood vessel:	n/a
3	chr7:111202450-111202500	NH-A	brain:	n/a
4	chr7:111202457-111202507	AoSMC	blood vessel:	n/a
5	chr7:110879415-110879465	A549	lung:	n/a
6	chr7:110906785-110906835	BE2_C	brain:	n/a
7	chr7:111200944-111200994	A549	lung:	n/a
8	chr7:111202395-111202445	SK-N-SH_RA	brain:	n/a
9	chr7:111202389-111202439	CMK	blood:	n/a
10	chr7:111202389-111202439	NH-A	brain:	n/a
11	chr7:110838461-110838511	GM06990	blood:	n/a
12	chr7:110906785-110906835	Caco-2	colon:	n/a
13	chr7:111033064-111033114	NB4	blood:	n/a
14	chr7:111086055-111086105	RPTEC	kidney:	n/a
15	chr7:111086055-111086105	HCM	heart:	n/a
16	chr7:111202666-111202716	U87	brain:	n/a
17	chr7:111202755-111202805	PrEC	prostate:	n/a
18	chr7:111202450-111202500	AG04449	skin:	fetal
19	chr7:111203008-111203058	U87	brain:	n/a
20	chr7:111202679-111202729	PrEC	prostate:	n/a
21	chr7:111202682-111202732	HepG2	liver:	n/a
22	chr7:111086055-111086105	HNPCEpiC	eye:	n/a
23	chr7:111249576-111249626	PFSK-1	brain:	n/a
24	chr7:111202457-111202507	K562	blood:	n/a
25	chr7:111202450-111202500	NB4	blood:	n/a
26	chr7:111202457-111202507	CMK	blood:	n/a
27	chr7:111249576-111249626	H1-hESC	embryonic stem cell:	embryo
28	chr7:111202666-111202716	NHDF-neo	bronchial:	n/a
29	chr7:111200944-111200994	BE2_C	brain:	n/a
30	chr7:111202679-111202729	GM06990	blood:	n/a
31	chr7:111249576-111249626	GM12878	blood:	n/a
32	chr7:111249576-111249626	HMEC	breast:	n/a
33	chr7:111202389-111202439	ECC-1	luminal epithelium:	n/a
34	chr7:111086055-111086105	HMEC	breast:	n/a
35	chr7:110906785-110906835	AG04450	lung:	fetal
36	chr7:111204826-111204876	HNPCEpiC	eye:	n/a
37	chr7:111202457-111202507	ProgFib	skin:	n/a
38	chr7:111200944-111200994	HUVEC	blood vessel:	n/a
39	chr7:110879415-110879465	HEK293	kidney:	embryo
40	chr7:110879415-110879465	Jurkat	blood:	n/a
41	chr7:111202389-111202439	Caco-2	colon:	n/a
42	chr7:110879415-110879465	SAEC	small airway:	n/a
43	chr7:111202679-111202729	HAEpiC	amniotic membrane:	n/a
44	chr7:110906785-110906835	HepG2	liver:	n/a
45	chr7:111249576-111249626	Hela-S3	cervix:	n/a
46	chr7:111202679-111202729	H1-hESC	embryonic stem cell:	embryo
47	chr7:111202389-111202439	HRCEpiC	kidney:	n/a
48	chr7:111202679-111202729	SK-N-SH_RA	brain:	n/a
49	chr7:111079100-111079150	PANC-1	pancreas:	n/a
50	chr7:111249924-111249974	H1-hESC	embryonic stem cell:	embryo

(count:351 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Distal block	Cell Line	Cell type
1	chr7:111179597..111181133-chr7:111200922..111203708,2	K562	blood:
2	chr7:110843665..110845702-chr7:110845783..110848771,2	K562	blood:
3	chr7:111106169..111107981-chr7:111111126..111114092,2	K562	blood:
4	chr7:110843665..110845702-chr7:110845783..110848771,2	K562	blood:
5	chr7:111183053..111185306-chr7:111210487..111212870,2	K562	blood:
6	chr7:111201180..111203639-chr7:116596222..116597858,2	MCF-7	breast:
7	chr7:111163636..111166513-chr7:111167048..111171015,5	K562	blood:
8	chr7:111134697..111137160-chr7:111200355..111203674,3	K562	blood:
9	chr7:110955341..110956918-chr7:110957234..110959729,2	K562	blood:
10	chr7:111132967..111134732-chr7:111137505..111139653,3	MCF-7	breast:
11	chr7:111222849..111225723-chr7:111230601..111232352,2	K562	blood:
12	chr7:110919285..110921892-chr7:110924129..110926222,2	K562	blood:
13	chr7:110843078..110844596-chr7:110851457..110854141,2	K562	blood:
14	chr7:111003207..111005251-chr7:111008050..111010228,2	K562	blood:
15	chr7:111020866..111024340-chr7:111025481..111028509,4	MCF-7	breast:
16	chr7:110865069..110867467-chr7:110870810..110872460,2	K562	blood:
17	chr7:110730162..110730849-chr7:111126372..111127229,2	MCF-7	breast:
18	chr7:111176200..111178839-chr7:111180322..111182875,3	K562	blood:
19	chr7:110962126..110964268-chr7:110964422..110967257,2	K562	blood:
20	chr7:110838767..110841477-chr7:110867993..110870087,3	K562	blood:
21	chr7:110876830..110878652-chr7:110880390..110881983,2	K562	blood:
22	chr7:111176200..111178839-chr7:111180322..111182875,3	K562	blood:
23	chr7:111173111..111178494-chr7:111200645..111202653,4	MCF-7	breast:
24	chr7:111164979..111167158-chr7:111168899..111171034,2	MCF-7	breast:
25	chr7:111164175..111171930-chr7:111196711..111203728,11	K562	blood:
26	chr7:110838767..110841477-chr7:110867993..110870087,3	K562	blood:
27	chr7:111096109..111097696-chr7:111100341..111102536,2	K562	blood:
28	chr7:111098758..111101723-chr7:111103712..111106818,3	K562	blood:
29	chr7:111014312..111015875-chr7:111016018..111018954,2	MCF-7	breast:
30	chr7:111165046..111169719-chr7:111171827..111173771,4	K562	blood:
31	chr7:111178053..111179952-chr7:111201249..111203327,2	MCF-7	breast:
32	chr7:111092714..111094433-chr7:111113503..111115872,2	K562	blood:
33	chr7:111252421..111255385-chr7:111257912..111259805,2	MCF-7	breast:
34	chr7:111238331..111240393-chr7:111247235..111250162,2	K562	blood:
35	chr7:111092714..111094433-chr7:111113503..111115872,2	K562	blood:
36	chr19:4065266..4065879-chr7:111202106..111203058,2	HCT-116	colon:
37	chr7:111043409..111046006-chr7:111053282..111056029,3	K562	blood:
38	chr7:110985007..110987369-chr7:110994363..110996141,2	K562	blood:
39	chr7:110838168..110840806-chr7:110845021..110846527,2	K562	blood:
40	chr7:111123975..111126506-chr7:111135381..111138359,2	K562	blood:
41	chr7:111001961..111006807-chr7:111013802..111016795,4	K562	blood:
42	chr7:111204432..111206292-chr7:111209030..111211645,2	K562	blood:
43	chr7:111001961..111006807-chr7:111013802..111016795,4	K562	blood:
44	chr7:111154605..111156613-chr7:111179034..111181673,2	K562	blood:
45	chr1:11967838..11968645-chr7:111201747..111202647,2	Hela-S3	cervix:
46	chr7:111150255..111152424-chr7:111159146..111160781,2	K562	blood:
47	chr7:110846458..110850024-chr7:110851219..110853852,3	MCF-7	breast:
48	chr7:111126326..111127035-chr7:111370303..111371090,2	MCF-7	breast:
49	chr6:31619932..31621913-chr7:111169935..111172752,2	K562	blood:
50	chr12:108200986..108203742-chr7:111052172..111055145,3	MCF-7	breast:

(count:3 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DOCK4-7	chr7:110902289-110902553	expReg_chr7_8342_-
2	lnc-LRRN3-2	chr7:111246670-111249064	ucscGeneNc_uc003vfz_2
3	lnc-LRRN3-2	chr7:111235830-111235905	ucscGeneNc_uc003vfz_2

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
ENSG00000143643	chromatin interactions
ENSG00000243621	chromatin interactions
ENSG00000126768	chromatin interactions
ENSG00000199347	chromatin interactions
ENSG00000188825	chromatin interactions
ENSG00000240053	chromatin interactions
ENSG00000141979	chromatin interactions
ENSG00000173409	chromatin interactions
ENSG00000204444	chromatin interactions
ENSG00000136856	chromatin interactions
ENSG00000184903	chromatin interactions
ENSG00000214188	chromatin interactions
ENSG00000164327	chromatin interactions
ENSG00000102103	chromatin interactions
ENSG00000105085	chromatin interactions
ENSG00000173114	chromatin interactions
ENSG00000178951	chromatin interactions
ENSG00000227948	chromatin interactions
ENSG00000173812	chromatin interactions
ENSG00000204463	chromatin interactions

Extended variants
information (count: 13909 )
Associated
traits (count: 102 )

Variant overlapped rSNPs/rCNVs (count:13909 , 50 per page) page: 1 2 3 4 5 6 7 ... 279

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs549943246	chr7:110835050-110835051	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs73714687	chr7:110835070-110835071	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs571846258	chr7:110835116-110835117	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs538691629	chr7:110835120-110835121	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs150857706	chr7:110835162-110835163	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs188821654	chr7:110835170-110835171	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs558534857	chr7:110835204-110835205	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs565507359	chr7:110835214-110835215	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs371274064	chr7:110835261-110835262	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs534532924	chr7:110835282-110835283	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs139229694	chr7:110835311-110835312	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs574208715	chr7:110835323-110835324	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs551156156	chr7:110835335-110835336	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs192667237	chr7:110835408-110835409	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs7779599	chr7:110835429-110835430	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs183369364	chr7:110835460-110835461	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs7798731	chr7:110835467-110835468	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs186910876	chr7:110835490-110835491	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs139995209	chr7:110835492-110835493	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs80133651	chr7:110835548-110835549	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs146074355	chr7:110835553-110835554	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs573223674	chr7:110835578-110835579	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs117515712	chr7:110835643-110835644	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs529962644	chr7:110835652-110835653	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs558857637	chr7:110835679-110835680	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs191278570	chr7:110835710-110835711	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs111235974	chr7:110835761-110835762	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs551958891	chr7:110835766-110835767	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs565701308	chr7:110835801-110835802	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs140343332	chr7:110835819-110835820	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs199769464	chr7:110835822-110835823	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs200610331	chr7:110835823-110835824	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs71151834	chr7:110835831-110835832	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs146487108	chr7:110835832-110835833	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs146117034	chr7:110835833-110835834	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs151234955	chr7:110835834-110835835	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs577015906	chr7:110835883-110835884	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs371276961	chr7:110835884-110835885	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs11974444	chr7:110835888-110835889	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs554487086	chr7:110835893-110835894	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs567613172	chr7:110835929-110835930	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs536500168	chr7:110835942-110835943	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs544403385	chr7:110835947-110835948	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs184852977	chr7:110835969-110835970	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs545118092	chr7:110836019-110836020	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs562305779	chr7:110836066-110836067	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs142099183	chr7:110836067-110836068	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs538288903	chr7:110836088-110836089	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs572444934	chr7:110836105-110836106	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs12533373	chr7:110836166-110836167	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:102)

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	21293372	CNVD
Dyslexia	22102821	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Attention deficit hyperactivity disorder	19546859	CNVD
Schizophrenia	23813976	CNVD
Autism	20531469	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	21509527	CNVD
Glioma	20126413	CNVD
early-passage human iPS cells	21368824	CNVD
Pancreatic cancer	17952125	CNVD
T-cell lymphomas	22341440	CNVD
Autism	20841430	CNVD
Autism	20685689	CNVD
Melanoma	20877625	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:2557 , 50 per page) page: 1 2 3 4 5 6 7 ... 52

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:110833400-110837800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr7:110835400-110837600	Weak transcription	HSMM	muscle
3	chr7:110836000-110836200	Enhancers	Psoas Muscle	Psoas
4	chr7:110836600-110836800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr7:110836800-110837600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr7:110837400-110838000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr7:110837400-110838200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
8	chr7:110837400-110840000	Enhancers	Muscle Satellite Cultured Cells	--
9	chr7:110837600-110837800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
10	chr7:110837600-110837800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
11	chr7:110837600-110838000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr7:110837600-110838000	Enhancers	NHDF-Ad	bronchial
13	chr7:110837600-110838200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
14	chr7:110837600-110839200	Enhancers	HMEC	breast
15	chr7:110837600-110839200	Enhancers	NH-A	brain
16	chr7:110837600-110839200	Enhancers	NHEK	skin
17	chr7:110837600-110839200	Enhancers	NHLF	lung
18	chr7:110837600-110839400	Enhancers	HSMM	muscle
19	chr7:110837600-110839800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
20	chr7:110837600-110840000	Enhancers	Osteobl	bone
21	chr7:110837800-110838200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
22	chr7:110837800-110838400	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
23	chr7:110837800-110838400	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
24	chr7:110837800-110838400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
25	chr7:110837800-110839000	Enhancers	Hela-S3	cervix
26	chr7:110838000-110838200	Enhancers	Skeletal Muscle Female	skeletal muscle
27	chr7:110838000-110838400	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
28	chr7:110838000-110838400	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr7:110838000-110838400	Flanking Active TSS	NHDF-Ad	bronchial
30	chr7:110838000-110838800	Enhancers	HSMMtube	muscle
31	chr7:110838200-110838600	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
32	chr7:110838200-110839000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
33	chr7:110838200-110846600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
34	chr7:110838400-110838600	Enhancers	Right Ventricle	heart
35	chr7:110838400-110838800	Enhancers	A549	lung
36	chr7:110838400-110839000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
37	chr7:110838400-110839200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
38	chr7:110838400-110839200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
39	chr7:110838400-110839600	Enhancers	NHDF-Ad	bronchial
40	chr7:110838400-110840200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
41	chr7:110838600-110838800	Enhancers	Skeletal Muscle Female	skeletal muscle
42	chr7:110838800-110864000	Weak transcription	Skeletal Muscle Female	skeletal muscle
43	chr7:110839000-110839200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
44	chr7:110839200-110839600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
45	chr7:110839600-110840000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
46	chr7:110842400-110842600	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
47	chr7:110842600-110852000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
48	chr7:110844400-110853000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
49	chr7:110845800-110846000	Enhancers	Left Ventricle	heart
50	chr7:110846000-110864000	Weak transcription	Left Ventricle	heart

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