Variant report

Variant	esv2756804
Chromosome Location	chr7:111056263-111261670
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2258)
CpG islands
(count:1038)
Chromatin interactive
region (count:176)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2258 , 50 per page) page: 1 2 3 4 5 6 7 ... 46

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:111202485-111202878	K562	blood:	n/a	n/a
2	ARID3A	chr7:111172220-111172476	K562	blood:	n/a	n/a
3	ARID3A	chr7:111150377-111150555	K562	blood:	n/a	n/a
4	ARID3A	chr7:111181171-111181430	HepG2	liver:	n/a	n/a
5	ARID3A	chr7:111199925-111200215	K562	blood:	n/a	n/a
6	ARID3A	chr7:111114444-111116392	K562	blood:	n/a	chr7:111115784-111115800 chr7:111114896-111114912 chr7:111114897-111114913
7	ARID3A	chr7:111118669-111118974	K562	blood:	n/a	n/a
8	ARID3A	chr7:111126348-111127214	K562	blood:	n/a	n/a
9	ARID3A	chr7:111064774-111065198	HepG2	liver:	n/a	n/a
10	ARID3A	chr7:111099362-111100398	K562	blood:	n/a	n/a
11	ARID3A	chr7:111202492-111202797	HepG2	liver:	n/a	n/a
12	ARID3A	chr7:111157885-111158000	HepG2	liver:	n/a	n/a
13	ARID3A	chr7:111100636-111100911	K562	blood:	n/a	chr7:111100841-111100857
14	ARID3A	chr7:111170171-111170509	HepG2	liver:	n/a	n/a
15	ARID3A	chr7:111202247-111202264	HepG2	liver:	n/a	n/a
16	ARID3A	chr7:111126639-111126960	HepG2	liver:	n/a	n/a
17	ARID3A	chr7:111116731-111117824	K562	blood:	n/a	n/a
18	ARID3A	chr7:111077670-111079453	K562	blood:	n/a	chr7:111078420-111078436 chr7:111078560-111078576
19	ATF1	chr7:111172136-111172453	K562	blood:	n/a	n/a
20	ATF1	chr7:111163232-111163327	K562	blood:	n/a	n/a
21	ATF1	chr7:111126656-111126990	K562	blood:	n/a	n/a
22	ATF1	chr7:111175451-111175458	K562	blood:	n/a	n/a
23	ATF1	chr7:111115090-111115592	K562	blood:	n/a	n/a
24	ATF1	chr7:111116070-111116343	K562	blood:	n/a	n/a
25	ATF1	chr7:111078600-111078973	K562	blood:	n/a	n/a
26	ATF1	chr7:111139180-111139448	K562	blood:	n/a	n/a
27	ATF2	chr7:111167522-111167997	GM12878	blood:	n/a	n/a
28	ATF2	chr7:111167450-111168045	GM12878	blood:	n/a	n/a
29	ATF2	chr7:111201787-111202190	H1-hESC	embryonic stem cell:	n/a	n/a
30	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
31	ATF3	chr7:111078506-111078989	K562	blood:	n/a	n/a
32	ATF3	chr7:111116052-111116358	K562	blood:	n/a	n/a
33	ATF3	chr7:111201918-111202678	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	chr7:111138942-111139670	A549	lung:	n/a	n/a
36	ATF3	chr7:111138963-111139597	A549	lung:	n/a	n/a
37	BACH1	chr7:111160755-111160869	K562	blood:	n/a	n/a
38	BACH1	chr7:111201779-111202839	K562	blood:	n/a	n/a
39	BACH1	chr7:111202015-111202410	H1-hESC	embryonic stem cell:	n/a	n/a
40	BACH1	chr7:111172186-111172416	K562	blood:	n/a	n/a
41	BACH1	chr7:111169257-111169277	K562	blood:	n/a	n/a
42	BACH1	chr7:111188905-111189076	K562	blood:	n/a	n/a
43	BATF	chr7:111228155-111228552	GM12878	blood:	n/a	chr7:111228280-111228290 chr7:111228384-111228394 chr7:111228383-111228394
44	BCL11A	chr7:111168484-111168730	GM12878	blood:	n/a	n/a
45	BCL3	chr7:111156597-111157052	A549	lung:	n/a	n/a
46	BCL3	chr7:111138913-111139703	A549	lung:	n/a	chr7:111138981-111138990
47	BCL3	chr7:111201738-111202909	A549	lung:	n/a	chr7:111202581-111202590 chr7:111202620-111202629 chr7:111202514-111202527 chr7:111202540-111202549
48	BCL3	chr7:111156319-111157358	A549	lung:	n/a	n/a
49	BCL3	chr7:111139024-111139659	A549	lung:	n/a	n/a
50	BCLAF1	chr7:111201762-111202357	GM12878	blood:	n/a	n/a

(count:1038 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:111202679-111202729	Hela-S3	cervix:	n/a
2	chr7:111202679-111202729	Hela-S3	cervix:	n/a
3	chr7:111202450-111202500	NHDF-neo	bronchial:	n/a
4	chr7:111198163-111198213	HNPCEpiC	eye:	n/a
5	chr7:111202679-111202729	GM06990	blood:	n/a
6	chr7:111198163-111198213	BJ	skin:	n/a
7	chr7:111202222-111202272	AG09319	gingival:	n/a
8	chr7:111202755-111202805	HEK293	kidney:	embryo
9	chr7:111202682-111202732	Hela-S3	cervix:	n/a
10	chr7:111202457-111202507	NHDF-neo	bronchial:	n/a
11	chr7:111086055-111086105	HIPEpiC	eye:	n/a
12	chr7:111249576-111249626	HRE	kidney:	n/a
13	chr7:111202682-111202732	SKMC	muscle:	n/a
14	chr7:111202457-111202507	HPAEpiC	pulmonary alveolar:	n/a
15	chr7:111202679-111202729	LNCaP	prostate:	n/a
16	chr7:111198163-111198213	NT2-D1	testis:	n/a
17	chr7:111202755-111202805	HIPEpiC	eye:	n/a
18	chr7:111086055-111086105	SAEC	small airway:	n/a
19	chr7:111079100-111079150	ProgFib	skin:	n/a
20	chr7:111203008-111203058	NT2-D1	testis:	n/a
21	chr7:111198163-111198213	PFSK-1	brain:	n/a
22	chr7:111202450-111202500	HUVEC	blood vessel:	n/a
23	chr7:111079100-111079150	HCT-116	colon:	n/a
24	chr7:111198163-111198213	NHBE	bronchial:	n/a
25	chr7:111079100-111079150	GM12892	blood:	n/a
26	chr7:111202755-111202805	NB4	blood:	n/a
27	chr7:111202389-111202439	HAEpiC	amniotic membrane:	n/a
28	chr7:111202389-111202439	HPAEpiC	pulmonary alveolar:	n/a
29	chr7:111204826-111204876	HCPEpiC	choroid plexus:	n/a
30	chr7:111204826-111204876	NHBE	bronchial:	n/a
31	chr7:111203008-111203058	NHDF-neo	bronchial:	n/a
32	chr7:111202395-111202445	ovcar-3	ovarian:	n/a
33	chr7:111202666-111202716	AG10803	skin:	n/a
34	chr7:111202450-111202500	HPAEpiC	pulmonary alveolar:	n/a
35	chr7:111204826-111204876	HepG2	liver:	n/a
36	chr7:111203008-111203058	AG04450	lung:	fetal
37	chr7:111079100-111079150	ECC-1	luminal epithelium:	n/a
38	chr7:111202666-111202716	SK-N-SH	brain:	n/a
39	chr7:111202450-111202500	HCM	heart:	n/a
40	chr7:111202666-111202716	MCF10A-Er-Src	breast:	n/a
41	chr7:111204826-111204876	MCF10A-Er-Src	breast:	n/a
42	chr7:111202389-111202439	AG10803	skin:	n/a
43	chr7:111202395-111202445	HRCEpiC	kidney:	n/a
44	chr7:111202389-111202439	AG09319	gingival:	n/a
45	chr7:111079100-111079150	GM19239	blood:	n/a
46	chr7:111202666-111202716	NHBE	bronchial:	n/a
47	chr7:111202222-111202272	GM12891	blood:	n/a
48	chr7:111198163-111198213	ovcar-3	ovarian:	n/a
49	chr7:111202755-111202805	HPAEpiC	pulmonary alveolar:	n/a
50	chr7:111203008-111203058	K562	blood:	n/a

(count:176 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type
1	chr7:111198400..111201071-chr7:111297443..111299093,2	K562	blood:
2	chr7:111167719..111169526-chr7:111174940..111178460,3	K562	blood:
3	chr7:111173111..111178494-chr7:111200645..111202653,4	MCF-7	breast:
4	chr7:111164149..111166792-chr7:111174165..111176807,3	K562	blood:
5	chr7:111164979..111167158-chr7:111168899..111171034,2	MCF-7	breast:
6	chr7:111067141..111070112-chr7:111198227..111201087,2	K562	blood:
7	chr7:111174213..111176704-chr7:111200682..111203644,3	K562	blood:
8	chr7:111226200..111228452-chr7:111228554..111231372,2	K562	blood:
9	chr7:111154283..111157202-chr7:111157997..111159947,2	MCF-7	breast:
10	chr7:111172229..111174380-chr7:111191411..111194309,2	K562	blood:
11	chr7:111100148..111100705-chr7:111129526..111130134,2	K562	blood:
12	chr7:111150770..111153588-chr7:111154725..111157322,3	K562	blood:
13	chr7:111075731..111078683-chr7:111110429..111113130,2	K562	blood:
14	chr7:111168569..111170226-chr7:111188051..111190882,2	K562	blood:
15	chr7:111132543..111134860-chr7:111136175..111139021,3	K562	blood:
16	chr7:111162292..111164581-chr7:111182567..111185234,2	K562	blood:
17	chr7:110730162..110730849-chr7:111126372..111127229,2	MCF-7	breast:
18	chr7:111164149..111167742-chr7:111173784..111176807,4	K562	blood:
19	chr7:111096109..111097696-chr7:111100341..111102536,2	K562	blood:
20	chr7:111134814..111136903-chr7:111375803..111377811,2	MCF-7	breast:
21	chr5:39074237..39075141-chr7:111201699..111202501,2	Hela-S3	cervix:
22	chr7:111176865..111178433-chr7:111182046..111183894,2	K562	blood:
23	chr7:111183053..111185306-chr7:111210487..111212870,2	K562	blood:
24	chr7:111067248..111069567-chr7:111070405..111074153,3	K562	blood:
25	chr7:111138086..111139591-chr7:111219192..111221961,2	MCF-7	breast:
26	chr7:111070056..111074231-chr7:111075733..111078781,4	K562	blood:
27	chr7:111050830..111052648-chr7:111066245..111068187,2	K562	blood:
28	chr7:111132543..111134860-chr7:111136175..111139021,3	K562	blood:
29	chr7:111165046..111167501-chr7:111171827..111173680,2	K562	blood:
30	chr7:111123279..111126052-chr7:111128693..111130965,2	K562	blood:
31	chr7:111166819..111169168-chr7:111191445..111193799,2	K562	blood:
32	chr7:111178493..111181177-chr7:111184776..111187564,2	K562	blood:
33	chr7:111163636..111166513-chr7:111167048..111171015,5	K562	blood:
34	chr7:111252421..111255385-chr7:111257912..111259805,2	MCF-7	breast:
35	chr7:111079252..111081356-chr7:111081507..111084110,2	K562	blood:
36	chr6:31639869..31641695-chr7:111180406..111182806,2	MCF-7	breast:
37	chr7:111222849..111225723-chr7:111230601..111232352,2	K562	blood:
38	chr7:111099278..111101723-chr7:111102972..111106150,5	K562	blood:
39	chr7:111178053..111179952-chr7:111201249..111203327,2	MCF-7	breast:
40	chr7:111123975..111126506-chr7:111135381..111138359,2	K562	blood:
41	chr7:111227327..111229119-chr7:111232502..111234968,2	K562	blood:
42	chr7:111174213..111177437-chr7:111200487..111202315,3	K562	blood:
43	chr7:111165046..111169719-chr7:111171827..111173771,4	K562	blood:
44	chr7:111164432..111166766-chr7:111167043..111169484,2	MCF-7	breast:
45	chr7:111238331..111240393-chr7:111247235..111250162,2	K562	blood:
46	chr7:111078917..111081356-chr7:111081507..111085373,3	K562	blood:
47	chr7:111092714..111094433-chr7:111113503..111115872,2	K562	blood:
48	chr7:111163636..111166513-chr7:111167048..111171015,5	K562	blood:
49	chr7:111134102..111136432-chr7:111201093..111203012,2	MCF-7	breast:
50	chr7:111067248..111069567-chr7:111070405..111074153,3	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
IMMP2L	TF binding region
IMMP2L	CpG island
ENSG00000173812	chromatin interactions
ENSG00000240053	chromatin interactions
ENSG00000214188	chromatin interactions
ENSG00000141979	chromatin interactions
ENSG00000204444	chromatin interactions
ENSG00000126768	chromatin interactions
ENSG00000204463	chromatin interactions
ENSG00000143643	chromatin interactions
ENSG00000199347	chromatin interactions
ENSG00000184903	chromatin interactions
ENSG00000105085	chromatin interactions
ENSG00000102103	chromatin interactions
ENSG00000178951	chromatin interactions
ENSG00000164327	chromatin interactions
ENSG00000227948	chromatin interactions
ENSG00000173114	chromatin interactions
ENSG00000173409	chromatin interactions

Extended variants
information (count: 6434 )
Associated
traits (count: 94 )

Variant overlapped rSNPs/rCNVs (count:6434 , 50 per page) page: 1 2 3 4 5 6 7 ... 129

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10232907	chr7:111056263-111056264	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs559454772	chr7:111056266-111056267	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs138416238	chr7:111056466-111056467	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs181074449	chr7:111056477-111056478	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs2106898	chr7:111056484-111056485	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs551225774	chr7:111056486-111056487	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs114233989	chr7:111056582-111056583	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs554524011	chr7:111056592-111056593	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs536974043	chr7:111056647-111056648	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs549341595	chr7:111056666-111056667	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs567592406	chr7:111056793-111056794	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs535114956	chr7:111056833-111056834	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs143816238	chr7:111056837-111056838	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs184310848	chr7:111056979-111056980	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs114881320	chr7:111057059-111057060	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs189871882	chr7:111057074-111057075	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs529273467	chr7:111057095-111057096	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs28489628	chr7:111057177-111057178	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs181027814	chr7:111057205-111057206	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs112052297	chr7:111057210-111057211	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs185944804	chr7:111057229-111057230	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs117370452	chr7:111057310-111057311	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs541082499	chr7:111057343-111057344	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs40372	chr7:111057345-111057346	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
25	rs553247652	chr7:111057372-111057373	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs551332984	chr7:111057373-111057374	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs116707636	chr7:111057375-111057376	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs112826759	chr7:111057383-111057384	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs549053289	chr7:111057416-111057417	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs190355916	chr7:111057430-111057431	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs569464894	chr7:111057481-111057482	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs147249196	chr7:111057505-111057506	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs80271305	chr7:111057535-111057536	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs571749141	chr7:111057537-111057538	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs539172202	chr7:111057557-111057558	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs557579335	chr7:111057585-111057586	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs376114289	chr7:111057607-111057608	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs181494114	chr7:111057614-111057615	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs139738430	chr7:111057617-111057618	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs533975032	chr7:111057623-111057624	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs548634351	chr7:111057635-111057636	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs573548816	chr7:111057637-111057638	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs113668677	chr7:111057653-111057654	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs540689714	chr7:111057659-111057660	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs186386859	chr7:111057660-111057661	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs143735583	chr7:111057671-111057672	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs372055379	chr7:111057672-111057673	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs575665090	chr7:111057690-111057691	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs370779545	chr7:111057836-111057837	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs374540443	chr7:111057847-111057848	Weak transcription	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
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
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
Cancer	20164919	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1486 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:111054200-111059600	Weak transcription	Aorta	Aorta
2	chr7:111054400-111059400	Weak transcription	Psoas Muscle	Psoas
3	chr7:111054800-111059200	Weak transcription	HUES64 Cell Line	embryonic stem cell
4	chr7:111055400-111064800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
5	chr7:111058400-111059200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr7:111059200-111059800	Enhancers	HUES64 Cell Line	embryonic stem cell
7	chr7:111059400-111059800	Enhancers	Psoas Muscle	Psoas
8	chr7:111059800-111066800	Weak transcription	Psoas Muscle	Psoas
9	chr7:111064200-111065400	Enhancers	HSMM	muscle
10	chr7:111064200-111065400	Enhancers	HSMMtube	muscle
11	chr7:111064200-111065400	Enhancers	NHDF-Ad	bronchial
12	chr7:111064400-111065400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
13	chr7:111064400-111065600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr7:111064400-111066000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
15	chr7:111064600-111065400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
16	chr7:111064600-111065400	Enhancers	Muscle Satellite Cultured Cells	--
17	chr7:111064600-111065600	Enhancers	NH-A	brain
18	chr7:111064800-111065200	Enhancers	ES-I3 Cell Line	embryonic stem cell
19	chr7:111064800-111065400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
20	chr7:111064800-111065400	Enhancers	HepG2	liver
21	chr7:111064800-111065400	Enhancers	HUVEC	blood vessel
22	chr7:111064800-111065600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
23	chr7:111064800-111065600	Enhancers	Hela-S3	cervix
24	chr7:111064800-111065600	Enhancers	Osteobl	bone
25	chr7:111065000-111065400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
26	chr7:111065000-111065400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
27	chr7:111065000-111065400	Enhancers	Fetal Lung	lung
28	chr7:111065200-111065400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
29	chr7:111065400-111069200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
30	chr7:111065400-111069400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
31	chr7:111065400-111069400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
32	chr7:111065400-111073000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
33	chr7:111065600-111069400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
34	chr7:111065600-111069600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
35	chr7:111065600-111078000	Weak transcription	Hela-S3	cervix
36	chr7:111067600-111068200	Active TSS	Pancreatic Islets	Pancreatic Islet
37	chr7:111069200-111069400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chr7:111069400-111069600	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
39	chr7:111069400-111069600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
40	chr7:111069400-111069800	Enhancers	A549	lung
41	chr7:111069400-111070000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
42	chr7:111069400-111070200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
43	chr7:111069600-111069800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
44	chr7:111069600-111070200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
45	chr7:111069600-111070200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
46	chr7:111069800-111070000	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
47	chr7:111069800-111075000	Weak transcription	Primary T helper cells fromperipheralblood	blood
48	chr7:111069800-111078600	Weak transcription	A549	lung
49	chr7:111070000-111070200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
50	chr7:111070200-111070400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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