Variant report

Variant	nsv1020409
Chromosome Location	chr7:110964519-111336737
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3301)
CpG islands
(count:1101)
Chromatin interactive
region (count:284)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:3301 , 50 per page) page: 1 2 3 4 5 6 7 ... 67

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	chr7:111181171-111181430	HepG2	liver:	n/a	n/a
4	ARID3A	chr7:111077670-111079453	K562	blood:	n/a	chr7:111078420-111078436 chr7:111078560-111078576
5	ARID3A	chr7:111172220-111172476	K562	blood:	n/a	n/a
6	ARID3A	chr7:111202492-111202797	HepG2	liver:	n/a	n/a
7	ARID3A	chr7:111099362-111100398	K562	blood:	n/a	n/a
8	ARID3A	chr7:111114444-111116392	K562	blood:	n/a	chr7:111115784-111115800 chr7:111114896-111114912 chr7:111114897-111114913
9	ARID3A	chr7:111150377-111150555	K562	blood:	n/a	n/a
10	ARID3A	chr7:111008626-111008764	K562	blood:	n/a	n/a
11	ARID3A	chr7:111290526-111290531	HepG2	liver:	n/a	n/a
12	ARID3A	chr7:111290764-111291175	HepG2	liver:	n/a	n/a
13	ARID3A	chr7:111202485-111202878	K562	blood:	n/a	n/a
14	ARID3A	chr7:111157885-111158000	HepG2	liver:	n/a	n/a
15	ARID3A	chr7:111024781-111024793	K562	blood:	n/a	n/a
16	ARID3A	chr7:110966486-110967469	K562	blood:	n/a	n/a
17	ARID3A	chr7:110968691-110969273	K562	blood:	n/a	n/a
18	ARID3A	chr7:111064774-111065198	HepG2	liver:	n/a	n/a
19	ARID3A	chr7:111126639-111126960	HepG2	liver:	n/a	n/a
20	ARID3A	chr7:110967767-110967878	K562	blood:	n/a	n/a
21	ARID3A	chr7:110969611-110970170	K562	blood:	n/a	n/a
22	ARID3A	chr7:110997534-110997571	K562	blood:	n/a	n/a
23	ARID3A	chr7:111202247-111202264	HepG2	liver:	n/a	n/a
24	ARID3A	chr7:111021038-111021344	HepG2	liver:	n/a	n/a
25	ARID3A	chr7:111199925-111200215	K562	blood:	n/a	n/a
26	ARID3A	chr7:111170171-111170509	HepG2	liver:	n/a	n/a
27	ARID3A	chr7:111126348-111127214	K562	blood:	n/a	n/a
28	ARID3A	chr7:111100636-111100911	K562	blood:	n/a	chr7:111100841-111100857
29	ARID3A	chr7:110968080-110968421	K562	blood:	n/a	n/a
30	ATF1	chr7:111335575-111335722	K562	blood:	n/a	n/a
31	ATF1	chr7:111319096-111319299	K562	blood:	n/a	n/a
32	ATF1	chr7:111163232-111163327	K562	blood:	n/a	n/a
33	ATF1	chr7:111175451-111175458	K562	blood:	n/a	n/a
34	ATF1	chr7:111172136-111172453	K562	blood:	n/a	n/a
35	ATF1	chr7:111116070-111116343	K562	blood:	n/a	n/a
36	ATF1	chr7:111054516-111054769	K562	blood:	n/a	n/a
37	ATF1	chr7:111115090-111115592	K562	blood:	n/a	n/a
38	ATF1	chr7:111078600-111078973	K562	blood:	n/a	n/a
39	ATF1	chr7:111126656-111126990	K562	blood:	n/a	n/a
40	ATF1	chr7:111012802-111012930	K562	blood:	n/a	n/a
41	ATF1	chr7:111139180-111139448	K562	blood:	n/a	n/a
42	ATF2	chr7:111053704-111054218	H1-hESC	embryonic stem cell:	n/a	n/a
43	ATF2	chr7:111201787-111202190	H1-hESC	embryonic stem cell:	n/a	n/a
44	ATF2	chr7:111167522-111167997	GM12878	blood:	n/a	n/a
45	ATF2	chr7:111167450-111168045	GM12878	blood:	n/a	n/a
46	ATF3	chr7:111116052-111116358	K562	blood:	n/a	n/a
47	ATF3	chr7:111201918-111202678	K562	blood:	n/a	n/a
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	chr7:111290708-111291147	A549	lung:	n/a	n/a

(count:1101 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:111203008-111203058	ProgFib	skin:	n/a
2	chr7:111204826-111204876	NB4	blood:	n/a
3	chr7:111202755-111202805	CMK	blood:	n/a
4	chr7:111203008-111203058	ProgFib	skin:	n/a
5	chr7:111204826-111204876	NB4	blood:	n/a
6	chr7:111202755-111202805	CMK	blood:	n/a
7	chr7:111249924-111249974	NT2-D1	testis:	n/a
8	chr7:111203008-111203058	HepG2	liver:	n/a
9	chr7:111202755-111202805	SK-N-SH_RA	brain:	n/a
10	chr7:111204826-111204876	HCPEpiC	choroid plexus:	n/a
11	chr7:111249924-111249974	K562	blood:	n/a
12	chr7:111033064-111033114	GM12878	blood:	n/a
13	chr7:111202395-111202445	MCF-7	breast:	n/a
14	chr7:111086055-111086105	RPTEC	kidney:	n/a
15	chr7:111202682-111202732	SAEC	small airway:	n/a
16	chr7:111202450-111202500	T-47D	breast:	n/a
17	chr7:111202755-111202805	SAEC	small airway:	n/a
18	chr7:111204826-111204876	HepG2	liver:	n/a
19	chr7:111202395-111202445	U87	brain:	n/a
20	chr7:111202666-111202716	AG09319	gingival:	n/a
21	chr7:111202457-111202507	SK-N-SH_RA	brain:	n/a
22	chr7:111202450-111202500	A549	lung:	n/a
23	chr7:111202222-111202272	A549	lung:	n/a
24	chr7:111202682-111202732	NT2-D1	testis:	n/a
25	chr7:111202682-111202732	IMR90	lung:	fetal
26	chr7:111203008-111203058	AoSMC	blood vessel:	n/a
27	chr7:111202395-111202445	Caco-2	colon:	n/a
28	chr7:111249924-111249974	MCF-7	breast:	n/a
29	chr7:111202457-111202507	MCF10A-Er-Src	breast:	n/a
30	chr7:111202222-111202272	NHBE	bronchial:	n/a
31	chr7:111202666-111202716	BJ	skin:	n/a
32	chr7:111202222-111202272	BJ	skin:	n/a
33	chr7:111202666-111202716	HCT-116	colon:	n/a
34	chr7:111033064-111033114	SAEC	small airway:	n/a
35	chr7:111202389-111202439	SAEC	small airway:	n/a
36	chr7:111202395-111202445	ovcar-3	ovarian:	n/a
37	chr7:111204826-111204876	Caco-2	colon:	n/a
38	chr7:111202395-111202445	GM12892	blood:	n/a
39	chr7:111202682-111202732	HPAEpiC	pulmonary alveolar:	n/a
40	chr7:111202450-111202500	SK-N-SH	brain:	n/a
41	chr7:111198163-111198213	NH-A	brain:	n/a
42	chr7:111202679-111202729	NB4	blood:	n/a
43	chr7:111202666-111202716	HepG2	liver:	n/a
44	chr7:111202755-111202805	K562	blood:	n/a
45	chr7:111204826-111204876	NHDF-neo	bronchial:	n/a
46	chr7:111204826-111204876	GM19239	blood:	n/a
47	chr7:111202389-111202439	HRE	kidney:	n/a
48	chr7:111086055-111086105	HAEpiC	amniotic membrane:	n/a
49	chr7:111202682-111202732	HRE	kidney:	n/a
50	chr7:111203008-111203058	Hela-S3	cervix:	n/a

(count:284 , 50 per page) page: 1 2 3 4 5 6

No.	Distal block	Cell Line	Cell type
1	chr7:111310577..111313223-chr7:111316574..111319309,2	K562	blood:
2	chr7:111178493..111181177-chr7:111184776..111187564,2	K562	blood:
3	chr7:110973996..110977417-chr7:110978130..110980823,3	K562	blood:
4	chr7:111025105..111026879-chr7:111027995..111029881,2	K562	blood:
5	chr7:110970635..110973843-chr7:110975141..110978905,5	K562	blood:
6	chr7:111299147..111302092-chr7:111316986..111318533,2	K562	blood:
7	chr7:110970018..110971875-chr7:110977199..110979815,2	K562	blood:
8	chr7:110969454..110970228-chr7:111375556..111376647,3	MCF-7	breast:
9	chr7:111172655..111174823-chr7:111200872..111202478,2	MCF-7	breast:
10	chr7:111138086..111139591-chr7:111219192..111221961,2	MCF-7	breast:
11	chr7:111123279..111126052-chr7:111128693..111130965,2	K562	blood:
12	chr7:111049337..111051671-chr7:111077981..111080558,2	K562	blood:
13	chr7:111150255..111152424-chr7:111159146..111160781,2	K562	blood:
14	chr7:111014312..111015875-chr7:111016018..111018954,2	MCF-7	breast:
15	chr7:111020866..111024340-chr7:111025481..111028509,4	MCF-7	breast:
16	chr7:110958175..110962470-chr7:110967524..110970471,4	K562	blood:
17	chr7:111167719..111169526-chr7:111174940..111178460,3	K562	blood:
18	chr7:111013152..111016122-chr7:111032306..111034572,2	K562	blood:
19	chr7:111227327..111229119-chr7:111232502..111234968,2	K562	blood:
20	chr7:111164979..111167158-chr7:111168899..111171034,2	MCF-7	breast:
21	chr7:111134102..111136432-chr7:111201093..111203012,2	MCF-7	breast:
22	chr7:111098758..111101723-chr7:111103712..111106818,3	K562	blood:
23	chr7:111132543..111134860-chr7:111136175..111139021,3	K562	blood:
24	chr7:108236133..108238229-chr7:111206520..111209026,2	K562	blood:
25	chr7:110958175..110961174-chr7:110967524..110969443,2	K562	blood:
26	chr7:111079252..111081356-chr7:111081507..111084110,2	K562	blood:
27	chr7:111111427..111114620-chr7:111124257..111128153,3	K562	blood:
28	chr7:111160191..111163357-chr7:111166833..111169527,4	K562	blood:
29	chr7:111114124..111115929-chr7:111199099..111201690,2	K562	blood:
30	chr7:111204432..111206292-chr7:111209030..111211645,2	K562	blood:
31	chr7:111098758..111101723-chr7:111103712..111106818,3	K562	blood:
32	chr7:111067248..111069567-chr7:111070405..111074153,3	K562	blood:
33	chr7:111226200..111228452-chr7:111228554..111231372,2	K562	blood:
34	chr7:111200608..111203822-chr7:111213514..111217285,4	K562	blood:
35	chr7:110969600..110972534-chr7:111078171..111081389,3	K562	blood:
36	chr7:111299093..111300961-chr7:111312313..111315147,2	K562	blood:
37	chr7:111156804..111158834-chr7:111201568..111203855,2	MCF-7	breast:
38	chr7:111020866..111024340-chr7:111025481..111028509,4	MCF-7	breast:
39	chr7:111166819..111169168-chr7:111191445..111193799,2	K562	blood:
40	chr7:111018295..111020688-chr7:111021531..111024788,3	MCF-7	breast:
41	chr7:110983062..110985792-chr7:110987528..110989399,4	K562	blood:
42	chr7:110994957..110999323-chr7:111001198..111006593,6	K562	blood:
43	chr7:111163636..111166513-chr7:111167048..111171015,5	K562	blood:
44	chr7:111162292..111164581-chr7:111182567..111185234,2	K562	blood:
45	chr7:110685337..110687591-chr7:111322599..111325063,2	K562	blood:
46	chr7:111186407..111189009-chr7:111189104..111191721,2	K562	blood:
47	chr7:111126326..111127035-chr7:111370303..111371090,2	MCF-7	breast:
48	chr7:111100148..111100705-chr7:111129526..111130134,2	K562	blood:
49	chr7:111018357..111021397-chr7:111023712..111026997,4	K562	blood:
50	chr7:110970635..110973843-chr7:110975141..110978905,5	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LRRN3-2	chr7:111235830-111235905	ucscGeneNc_uc003vfz_2
2	lnc-LRRN3-2	chr7:111246670-111249064	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
ENSG00000178951	chromatin interactions
ENSG00000227948	chromatin interactions
ENSG00000105085	chromatin interactions
ENSG00000188825	chromatin interactions
ENSG00000143643	chromatin interactions
ENSG00000199347	chromatin interactions
ENSG00000204463	chromatin interactions
ENSG00000126768	chromatin interactions
ENSG00000214188	chromatin interactions
ENSG00000141979	chromatin interactions
ENSG00000164327	chromatin interactions
ENSG00000204444	chromatin interactions
ENSG00000173114	chromatin interactions
ENSG00000173812	chromatin interactions
ENSG00000240053	chromatin interactions
ENSG00000243621	chromatin interactions
ENSG00000173409	chromatin interactions
ENSG00000102103	chromatin interactions
ENSG00000184903	chromatin interactions

Extended variants
information (count: 11325 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:11325 , 50 per page) page: 1 2 3 4 5 6 7 ... 227

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs534319910	chr7:110964551-110964552	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs552755642	chr7:110964574-110964575	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs555655422	chr7:110964641-110964642	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs116249574	chr7:110964667-110964668	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs563476167	chr7:110964676-110964677	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs575544968	chr7:110964725-110964726	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs542910674	chr7:110964737-110964738	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs528119285	chr7:110964742-110964743	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs561189608	chr7:110964745-110964746	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs34493751	chr7:110964765-110964766	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs186124555	chr7:110964808-110964809	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs547006144	chr7:110964812-110964813	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs190600919	chr7:110964904-110964905	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs146356442	chr7:110964919-110964920	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs181493523	chr7:110964962-110964963	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs534326969	chr7:110964968-110964969	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs374361590	chr7:110965194-110965195	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs185339088	chr7:110965240-110965241	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs557515311	chr7:110965277-110965278	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs536467366	chr7:110965297-110965298	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs55671609	chr7:110965343-110965344	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs548425483	chr7:110965415-110965416	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs566834032	chr7:110965437-110965438	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs148561393	chr7:110965446-110965447	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs115425706	chr7:110965456-110965457	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs577597978	chr7:110965458-110965459	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs538712400	chr7:110965459-110965460	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs534783897	chr7:110965520-110965521	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs556796222	chr7:110965598-110965599	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs552817072	chr7:110965610-110965611	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs575483943	chr7:110965627-110965628	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs542849312	chr7:110965641-110965642	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs141872335	chr7:110965665-110965666	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs190052118	chr7:110965669-110965670	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs577445612	chr7:110965777-110965778	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs373329659	chr7:110965789-110965790	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs565267081	chr7:110965794-110965795	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs532414855	chr7:110965806-110965807	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs551022238	chr7:110965807-110965808	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs150639352	chr7:110965842-110965843	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs530190875	chr7:110965849-110965850	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs548365926	chr7:110965863-110965864	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs566772698	chr7:110965905-110965906	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs534202435	chr7:110965978-110965979	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs552629120	chr7:110966075-110966076	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs571189000	chr7:110966135-110966136	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs577696238	chr7:110966142-110966143	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs139823914	chr7:110966149-110966150	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs149765554	chr7:110966180-110966181	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs568963055	chr7:110966214-110966215	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:95)

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
Melanoma	20877625	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:2068 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:110960000-110983400	Weak transcription	Left Ventricle	heart
2	chr7:110962600-110967200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr7:110964200-110964600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
4	chr7:110964200-110964600	Enhancers	Monocytes-CD14+_RO01746	blood
5	chr7:110964600-110967200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
6	chr7:110964600-110969000	Weak transcription	Monocytes-CD14+_RO01746	blood
7	chr7:110966400-110966600	Active TSS	K562	blood
8	chr7:110966600-110966800	Flanking Active TSS	K562	blood
9	chr7:110966800-110967000	Active TSS	K562	blood
10	chr7:110967000-110967400	Flanking Active TSS	K562	blood
11	chr7:110967200-110968800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr7:110967200-110969000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
13	chr7:110967400-110969400	Active TSS	K562	blood
14	chr7:110968400-110973000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr7:110968600-110968800	Enhancers	GM12878-XiMat	blood
16	chr7:110968800-110969200	Flanking Active TSS	GM12878-XiMat	blood
17	chr7:110968800-110969800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
18	chr7:110969000-110969600	Enhancers	Monocytes-CD14+_RO01746	blood
19	chr7:110969000-110969800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
20	chr7:110969200-110969600	Enhancers	Primary monocytes fromperipheralblood	blood
21	chr7:110969200-110970400	Enhancers	GM12878-XiMat	blood
22	chr7:110969400-110970000	Flanking Active TSS	K562	blood
23	chr7:110971200-110971400	Enhancers	Adipose Nuclei	Adipose
24	chr7:110971400-110978800	Weak transcription	Adipose Nuclei	Adipose
25	chr7:110973000-110973600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
26	chr7:110973000-110973600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
27	chr7:110973000-110973600	Enhancers	HMEC	breast
28	chr7:110973000-110973800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
29	chr7:110973000-110973800	Enhancers	NHEK	skin
30	chr7:110973600-110979800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
31	chr7:110973800-110983400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
32	chr7:110978000-110978200	Enhancers	Psoas Muscle	Psoas
33	chr7:110978800-110979200	Enhancers	Adipose Nuclei	Adipose
34	chr7:110978800-110979400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
35	chr7:110978800-110979400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
36	chr7:110978800-110979400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
37	chr7:110978800-110979800	Enhancers	Pancreatic Islets	Pancreatic Islet
38	chr7:110979400-110981600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
39	chr7:110979800-110980800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
40	chr7:110980400-110981000	Enhancers	NHEK	skin
41	chr7:110980800-110983200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
42	chr7:110981600-110982000	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
43	chr7:110983200-110983600	ZNF genes & repeats	Foreskin Keratinocyte Primary Cells skin03	Skin
44	chr7:110983400-110983600	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
45	chr7:110983400-110983600	ZNF genes & repeats	Left Ventricle	heart
46	chr7:110983400-110983800	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
47	chr7:110983600-110984200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
48	chr7:110984000-110985600	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
49	chr7:110987000-110987800	Enhancers	Psoas Muscle	Psoas
50	chr7:110987400-111002800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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