Variant report

Variant	nsv1022408
Chromosome Location	chr7:110978196-111194233
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1813)
CpG islands
(count:183)
Chromatin interactive
region (count:191)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1813 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:111114444-111116392	K562	blood:	n/a	chr7:111115784-111115800 chr7:111114896-111114912 chr7:111114897-111114913
2	ARID3A	chr7:111126639-111126960	HepG2	liver:	n/a	n/a
3	ARID3A	chr7:110997534-110997571	K562	blood:	n/a	n/a
4	ARID3A	chr7:111008626-111008764	K562	blood:	n/a	n/a
5	ARID3A	chr7:111099362-111100398	K562	blood:	n/a	n/a
6	ARID3A	chr7:111181171-111181430	HepG2	liver:	n/a	n/a
7	ARID3A	chr7:111021038-111021344	HepG2	liver:	n/a	n/a
8	ARID3A	chr7:111116731-111117824	K562	blood:	n/a	n/a
9	ARID3A	chr7:111064774-111065198	HepG2	liver:	n/a	n/a
10	ARID3A	chr7:111077670-111079453	K562	blood:	n/a	chr7:111078420-111078436 chr7:111078560-111078576
11	ARID3A	chr7:111157885-111158000	HepG2	liver:	n/a	n/a
12	ARID3A	chr7:111100636-111100911	K562	blood:	n/a	chr7:111100841-111100857
13	ARID3A	chr7:111126348-111127214	K562	blood:	n/a	n/a
14	ARID3A	chr7:111172220-111172476	K562	blood:	n/a	n/a
15	ARID3A	chr7:111170171-111170509	HepG2	liver:	n/a	n/a
16	ARID3A	chr7:111150377-111150555	K562	blood:	n/a	n/a
17	ARID3A	chr7:111118669-111118974	K562	blood:	n/a	n/a
18	ARID3A	chr7:111024781-111024793	K562	blood:	n/a	n/a
19	ATF1	chr7:111175451-111175458	K562	blood:	n/a	n/a
20	ATF1	chr7:111172136-111172453	K562	blood:	n/a	n/a
21	ATF1	chr7:111126656-111126990	K562	blood:	n/a	n/a
22	ATF1	chr7:111054516-111054769	K562	blood:	n/a	n/a
23	ATF1	chr7:111139180-111139448	K562	blood:	n/a	n/a
24	ATF1	chr7:111012802-111012930	K562	blood:	n/a	n/a
25	ATF1	chr7:111078600-111078973	K562	blood:	n/a	n/a
26	ATF1	chr7:111116070-111116343	K562	blood:	n/a	n/a
27	ATF1	chr7:111163232-111163327	K562	blood:	n/a	n/a
28	ATF1	chr7:111115090-111115592	K562	blood:	n/a	n/a
29	ATF2	chr7:111053704-111054218	H1-hESC	embryonic stem cell:	n/a	n/a
30	ATF2	chr7:111167450-111168045	GM12878	blood:	n/a	n/a
31	ATF2	chr7:111167522-111167997	GM12878	blood:	n/a	n/a
32	ATF3	chr7:111138942-111139670	A549	lung:	n/a	n/a
33	ATF3	chr7:111116052-111116358	K562	blood:	n/a	n/a
34	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
35	ATF3	chr7:111138963-111139597	A549	lung:	n/a	n/a
36	ATF3	chr7:111078506-111078989	K562	blood:	n/a	n/a
37	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
38	BACH1	chr7:111169257-111169277	K562	blood:	n/a	n/a
39	BACH1	chr7:111188905-111189076	K562	blood:	n/a	n/a
40	BACH1	chr7:111172186-111172416	K562	blood:	n/a	n/a
41	BACH1	chr7:111160755-111160869	K562	blood:	n/a	n/a
42	BATF	chr7:110992517-110992735	GM12878	blood:	n/a	n/a
43	BATF	chr7:111029015-111029334	GM12878	blood:	n/a	n/a
44	BCL11A	chr7:111029036-111029324	GM12878	blood:	n/a	n/a
45	BCL11A	chr7:111168484-111168730	GM12878	blood:	n/a	n/a
46	BCL3	chr7:111139024-111139659	A549	lung:	n/a	n/a
47	BCL3	chr7:111138913-111139703	A549	lung:	n/a	chr7:111138981-111138990
48	BCL3	chr7:111156597-111157052	A549	lung:	n/a	n/a
49	BCL3	chr7:111156319-111157358	A549	lung:	n/a	n/a
50	BCLAF1	chr7:111168247-111168782	GM12878	blood:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:111079100-111079150	HAEpiC	amniotic membrane:	n/a
2	chr7:111086055-111086105	GM12892	blood:	n/a
3	chr7:111086055-111086105	SK-N-SH_RA	brain:	n/a
4	chr7:111079100-111079150	SKMC	muscle:	n/a
5	chr7:111079100-111079150	H1-hESC	embryonic stem cell:	embryo
6	chr7:111079100-111079150	PrEC	prostate:	n/a
7	chr7:111079100-111079150	SK-N-SH_RA	brain:	n/a
8	chr7:111033064-111033114	ECC-1	luminal epithelium:	n/a
9	chr7:111086055-111086105	SAEC	small airway:	n/a
10	chr7:111033064-111033114	GM12878	blood:	n/a
11	chr7:111086055-111086105	ProgFib	skin:	n/a
12	chr7:111086055-111086105	K562	blood:	n/a
13	chr7:111033064-111033114	PFSK-1	brain:	n/a
14	chr7:111086055-111086105	HAEpiC	amniotic membrane:	n/a
15	chr7:111033064-111033114	SK-N-MC	brain:	n/a
16	chr7:111079100-111079150	HCPEpiC	choroid plexus:	n/a
17	chr7:111079100-111079150	ProgFib	skin:	n/a
18	chr7:111033064-111033114	HCF	heart:	n/a
19	chr7:111033064-111033114	HCM	heart:	n/a
20	chr7:111086055-111086105	HEEpiC	esophagus:	n/a
21	chr7:111079100-111079150	HCM	heart:	n/a
22	chr7:111079100-111079150	SAEC	small airway:	n/a
23	chr7:111086055-111086105	HIPEpiC	eye:	n/a
24	chr7:111086055-111086105	Hela-S3	cervix:	n/a
25	chr7:111079100-111079150	HNPCEpiC	eye:	n/a
26	chr7:111079100-111079150	LNCaP	prostate:	n/a
27	chr7:111086055-111086105	HCM	heart:	n/a
28	chr7:111079100-111079150	HRE	kidney:	n/a
29	chr7:111033064-111033114	HUVEC	blood vessel:	n/a
30	chr7:111079100-111079150	AoSMC	blood vessel:	n/a
31	chr7:111033064-111033114	NB4	blood:	n/a
32	chr7:111079100-111079150	ovcar-3	ovarian:	n/a
33	chr7:111033064-111033114	NT2-D1	testis:	n/a
34	chr7:111086055-111086105	CMK	blood:	n/a
35	chr7:111079100-111079150	T-47D	breast:	n/a
36	chr7:111086055-111086105	ECC-1	luminal epithelium:	n/a
37	chr7:111079100-111079150	Hela-S3	cervix:	n/a
38	chr7:111033064-111033114	HEEpiC	esophagus:	n/a
39	chr7:111079100-111079150	CMK	blood:	n/a
40	chr7:111079100-111079150	RPTEC	kidney:	n/a
41	chr7:111079100-111079150	NB4	blood:	n/a
42	chr7:111086055-111086105	AG04449	skin:	fetal
43	chr7:111086055-111086105	AG04450	lung:	fetal
44	chr7:111086055-111086105	BE2_C	brain:	n/a
45	chr7:111079100-111079150	BJ	skin:	n/a
46	chr7:111079100-111079150	MCF-7	breast:	n/a
47	chr7:111033064-111033114	RPTEC	kidney:	n/a
48	chr7:111033064-111033114	Hela-S3	cervix:	n/a
49	chr7:111079100-111079150	NT2-D1	testis:	n/a
50	chr7:111086055-111086105	U87	brain:	n/a

(count:191 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type
1	chr7:111099286..111101229-chr7:111113848..111115387,2	K562	blood:
2	chr7:111159302..111161681-chr7:111166227..111168647,2	MCF-7	breast:
3	chr7:111164979..111167158-chr7:111168899..111171034,2	MCF-7	breast:
4	chr7:111099286..111101229-chr7:111113848..111115387,2	K562	blood:
5	chr7:111136494..111138259-chr7:111146295..111147835,2	K562	blood:
6	chr7:111067141..111070112-chr7:111198227..111201087,2	K562	blood:
7	chr7:111051033..111052648-chr7:111065834..111068187,2	K562	blood:
8	chr7:111018295..111020688-chr7:111021531..111024788,3	MCF-7	breast:
9	chr7:110946954..110949529-chr7:111129446..111130953,2	MCF-7	breast:
10	chr7:111138086..111139591-chr7:111219192..111221961,2	MCF-7	breast:
11	chr7:111167719..111169526-chr7:111174940..111178460,3	K562	blood:
12	chr7:110924808..110925532-chr7:111126328..111127072,2	MCF-7	breast:
13	chr7:111014312..111015875-chr7:111016018..111018954,2	MCF-7	breast:
14	chr7:110973996..110977417-chr7:110978130..110980823,3	K562	blood:
15	chr7:111033619..111035253-chr7:111039961..111041629,2	K562	blood:
16	chr7:111092714..111094433-chr7:111113503..111115872,2	K562	blood:
17	chr7:111043409..111046006-chr7:111053282..111056029,3	K562	blood:
18	chr7:111003207..111005251-chr7:111008050..111010228,2	K562	blood:
19	chr7:111013152..111016122-chr7:111032306..111034572,2	K562	blood:
20	chr7:111158021..111159788-chr7:111160191..111162474,2	K562	blood:
21	chr7:111079252..111081356-chr7:111081507..111084110,2	K562	blood:
22	chr7:111106169..111107981-chr7:111111126..111114092,2	K562	blood:
23	chr7:111164149..111167742-chr7:111173784..111176807,4	K562	blood:
24	chr7:111098758..111101723-chr7:111103712..111106818,3	K562	blood:
25	chr7:111033479..111035253-chr7:111039939..111041629,3	K562	blood:
26	chr17:41463788..41465299-chr7:111034758..111036259,2	K562	blood:
27	chr7:110978869..110982048-chr7:110982767..110985792,3	K562	blood:
28	chr7:110969852..110970371-chr7:111126745..111127278,2	K562	blood:
29	chr7:110970635..110973843-chr7:110975141..110978905,5	K562	blood:
30	chr7:110994535..110996072-chr7:110997457..110999303,2	K562	blood:
31	chr7:111176865..111178433-chr7:111182046..111183894,2	K562	blood:
32	chr7:111150255..111152424-chr7:111159146..111160781,2	K562	blood:
33	chr7:111163636..111166513-chr7:111167048..111171015,5	K562	blood:
34	chr7:111181285..111183708-chr7:111185192..111188559,3	K562	blood:
35	chr7:110983062..110985792-chr7:110987528..110989399,4	K562	blood:
36	chr7:111165046..111169719-chr7:111171827..111173771,4	K562	blood:
37	chr7:110911704..110914495-chr7:111113882..111116767,2	K562	blood:
38	chr7:110977304..110981066-chr7:110982767..110987604,6	K562	blood:
39	chr7:111017537..111020347-chr7:111082285..111084321,2	K562	blood:
40	chr7:111050830..111052648-chr7:111066245..111068187,2	K562	blood:
41	chr7:111172393..111173981-chr7:111189118..111191154,2	K562	blood:
42	chr7:111173111..111178494-chr7:111200645..111202653,4	MCF-7	breast:
43	chr7:111136494..111138259-chr7:111146295..111147835,2	K562	blood:
44	chr7:111049337..111051671-chr7:111077981..111080558,2	K562	blood:
45	chr7:111099278..111101723-chr7:111102972..111106150,5	K562	blood:
46	chr7:111050112..111052168-chr7:111053965..111056674,3	K562	blood:
47	chr7:111132967..111134732-chr7:111137505..111139653,3	MCF-7	breast:
48	chr7:111165987..111169659-chr7:111199981..111202962,6	K562	blood:
49	chr7:110730162..110730849-chr7:111126372..111127229,2	MCF-7	breast:
50	chr7:111106169..111107981-chr7:111111126..111114092,2	K562	blood:

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
ENSG00000240053	chromatin interactions
ENSG00000204463	chromatin interactions
ENSG00000204444	chromatin interactions
ENSG00000184903	chromatin interactions
ENSG00000173114	chromatin interactions
ENSG00000243621	chromatin interactions
ENSG00000173409	chromatin interactions
ENSG00000227948	chromatin interactions
ENSG00000143643	chromatin interactions

Extended variants
information (count: 7732 )
Associated
traits (count: 94 )

Variant overlapped rSNPs/rCNVs (count:7732 , 50 per page) page: 1 2 3 4 5 6 7 ... 155

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs185210540	chr7:110978218-110978219	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs140305767	chr7:110978259-110978260	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs563553761	chr7:110978269-110978270	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs555172271	chr7:110978292-110978293	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs573739775	chr7:110978330-110978331	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs539387688	chr7:110978353-110978354	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs371897192	chr7:110978378-110978379	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs540858321	chr7:110978380-110978381	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs553250974	chr7:110978402-110978403	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs577982800	chr7:110978449-110978450	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs188887420	chr7:110978555-110978556	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs575646650	chr7:110978557-110978558	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs557640644	chr7:110978623-110978624	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs530952271	chr7:110978641-110978642	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs543063086	chr7:110978698-110978699	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs10277071	chr7:110978703-110978704	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs528628972	chr7:110978710-110978711	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs575806340	chr7:110978712-110978713	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs546877963	chr7:110978750-110978751	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs181991776	chr7:110978766-110978767	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs532629782	chr7:110978794-110978795	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs186327431	chr7:110978802-110978803	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs550882090	chr7:110978818-110978819	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs75813991	chr7:110978839-110978840	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs75463686	chr7:110978847-110978848	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs6957826	chr7:110978882-110978883	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs143982391	chr7:110978900-110978901	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs190980091	chr7:110978952-110978953	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs534743596	chr7:110978973-110978974	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs553187857	chr7:110978992-110978993	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs577929020	chr7:110979046-110979047	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs545296334	chr7:110979047-110979048	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs557297909	chr7:110979048-110979049	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs575556450	chr7:110979063-110979064	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs542648751	chr7:110979094-110979095	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs549656164	chr7:110979147-110979148	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs540711698	chr7:110979200-110979201	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs559785577	chr7:110979234-110979235	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs528559709	chr7:110979275-110979276	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs72281664	chr7:110979316-110979317	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs540341310	chr7:110979341-110979342	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs35744534	chr7:110979353-110979354	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs565105391	chr7:110979375-110979376	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs532567473	chr7:110979388-110979389	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs550820453	chr7:110979391-110979392	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs180981840	chr7:110979457-110979458	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs562831378	chr7:110979484-110979485	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs530471886	chr7:110979492-110979493	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs528828004	chr7:110979509-110979510	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs10251630	chr7:110979556-110979557	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:94)

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

Chromatin state (count:1329 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:110960000-110983400	Weak transcription	Left Ventricle	heart
2	chr7:110971400-110978800	Weak transcription	Adipose Nuclei	Adipose
3	chr7:110973600-110979800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
4	chr7:110973800-110983400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr7:110978000-110978200	Enhancers	Psoas Muscle	Psoas
6	chr7:110978800-110979200	Enhancers	Adipose Nuclei	Adipose
7	chr7:110978800-110979400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
8	chr7:110978800-110979400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
9	chr7:110978800-110979400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chr7:110978800-110979800	Enhancers	Pancreatic Islets	Pancreatic Islet
11	chr7:110979400-110981600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr7:110979800-110980800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
13	chr7:110980400-110981000	Enhancers	NHEK	skin
14	chr7:110980800-110983200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
15	chr7:110981600-110982000	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr7:110983200-110983600	ZNF genes & repeats	Foreskin Keratinocyte Primary Cells skin03	Skin
17	chr7:110983400-110983600	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
18	chr7:110983400-110983600	ZNF genes & repeats	Left Ventricle	heart
19	chr7:110983400-110983800	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
20	chr7:110983600-110984200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
21	chr7:110984000-110985600	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
22	chr7:110987000-110987800	Enhancers	Psoas Muscle	Psoas
23	chr7:110987400-111002800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
24	chr7:110987800-110989600	Weak transcription	Psoas Muscle	Psoas
25	chr7:110989600-110989800	Enhancers	Psoas Muscle	Psoas
26	chr7:110996800-110997400	Enhancers	K562	blood
27	chr7:110997000-110997200	Enhancers	Skeletal Muscle Female	skeletal muscle
28	chr7:110997000-110997200	Enhancers	HSMMtube	muscle
29	chr7:110997000-110997800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
30	chr7:110997000-110998200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
31	chr7:110997000-110998400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
32	chr7:110997000-110998600	Enhancers	A549	lung
33	chr7:110997000-110998800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
34	chr7:110997000-110999000	Enhancers	HMEC	breast
35	chr7:110997000-110999200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
36	chr7:110997000-110999200	Enhancers	Hela-S3	cervix
37	chr7:110997000-110999400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
38	chr7:110997000-110999800	Enhancers	Breast Myoepithelial Primary Cells	Breast
39	chr7:110997200-110997400	Enhancers	NH-A	brain
40	chr7:110997200-110998000	Weak transcription	HSMMtube	muscle
41	chr7:110997200-110998200	Weak transcription	Skeletal Muscle Female	skeletal muscle
42	chr7:110997200-110998200	Enhancers	Osteobl	bone
43	chr7:110997200-110998400	Enhancers	HSMM	muscle
44	chr7:110997200-110998600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
45	chr7:110997200-110999200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
46	chr7:110997400-110998000	Enhancers	NHEK	skin
47	chr7:110997400-110998400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
48	chr7:110997400-110998400	Enhancers	NHDF-Ad	bronchial
49	chr7:110997400-111002800	Weak transcription	NH-A	brain
50	chr7:110997400-111008200	Weak transcription	K562	blood

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