Variant report

Variant	nsv1034375
Chromosome Location	chr7:111337109-111459099
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1737)
CpG islands
(count:976)
Chromatin interactive
region (count:122)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1737 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:111375799-111376068	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:111443491-111443697	HepG2	liver:	n/a	n/a
3	ARID3A	chr7:111392302-111392575	HepG2	liver:	n/a	n/a
4	ARID3A	chr7:111392192-111392559	K562	blood:	n/a	n/a
5	ARID3A	chr7:111403332-111403618	HepG2	liver:	n/a	n/a
6	ARID3A	chr7:111370466-111370966	K562	blood:	n/a	n/a
7	ATF1	chr7:111375748-111376065	K562	blood:	n/a	n/a
8	ATF1	chr7:111368182-111368195	K562	blood:	n/a	n/a
9	ATF1	chr7:111381738-111382134	K562	blood:	n/a	n/a
10	ATF3	chr7:111375696-111376126	K562	blood:	n/a	n/a
11	BACH1	chr7:111396984-111397236	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr7:111386460-111386469	K562	blood:	n/a	n/a
13	BACH1	chr7:111392284-111392512	K562	blood:	n/a	n/a
14	BATF	chr7:111375766-111375996	GM12878	blood:	n/a	chr7:111375898-111375908
15	BHLHE40	chr7:111436856-111436982	K562	blood:	n/a	n/a
16	BHLHE40	chr7:111370404-111370936	K562	blood:	n/a	n/a
17	BHLHE40	chr7:111386532-111386636	K562	blood:	n/a	n/a
18	BHLHE40	chr7:111392303-111392547	GM12878	blood:	n/a	n/a
19	BHLHE40	chr7:111369140-111369236	K562	blood:	n/a	n/a
20	BHLHE40	chr7:111408231-111408271	K562	blood:	n/a	n/a
21	BHLHE40	chr7:111381712-111382240	K562	blood:	n/a	n/a
22	BHLHE40	chr7:111373440-111373553	K562	blood:	n/a	n/a
23	BHLHE40	chr7:111392265-111392570	K562	blood:	n/a	n/a
24	BRCA1	chr7:111433151-111433155	Hela-S3	cervix:	n/a	n/a
25	BRCA1	chr7:111381965-111382012	GM12878	blood:	n/a	n/a
26	BRCA1	chr7:111381752-111382173	Hela-S3	cervix:	n/a	n/a
27	CBX3	chr7:111436678-111437131	K562	blood:	n/a	n/a
28	CBX3	chr7:111436751-111437276	K562	blood:	n/a	n/a
29	CBX3	chr7:111436695-111437223	HCT-116	colon:	n/a	n/a
30	CBX3	chr7:111436763-111437097	HCT-116	colon:	n/a	n/a
31	CCNT2	chr7:111446301-111446437	K562	blood:	n/a	n/a
32	CEBPB	chr7:111368141-111368225	H1-hESC	embryonic stem cell:	n/a	chr7:111368176-111368187
33	CEBPB	chr7:111454820-111455020	H1-hESC	embryonic stem cell:	n/a	n/a
34	CEBPB	chr7:111384597-111385184	IMR90	lung:	n/a	chr7:111384757-111384770 chr7:111384759-111384770 chr7:111384757-111384768 chr7:111384757-111384770
35	CEBPB	chr7:111381851-111382120	H1-hESC	embryonic stem cell:	n/a	n/a
36	CEBPB	chr7:111384599-111384948	K562	blood:	n/a	chr7:111384757-111384770 chr7:111384759-111384770 chr7:111384757-111384768 chr7:111384757-111384770
37	CEBPB	chr7:111446290-111446634	HepG2	liver:	n/a	chr7:111446448-111446457 chr7:111446446-111446459 chr7:111446446-111446457
38	CEBPB	chr7:111411474-111411776	K562	blood:	n/a	chr7:111411619-111411630
39	CEBPB	chr7:111375637-111376090	Hela-S3	cervix:	n/a	chr7:111375805-111375816
40	CEBPB	chr7:111397030-111397229	K562	blood:	n/a	n/a
41	CEBPB	chr7:111411478-111411691	A549	lung:	n/a	chr7:111411619-111411630
42	CEBPB	chr7:111367134-111367313	K562	blood:	n/a	chr7:111367217-111367228
43	CEBPB	chr7:111411489-111411748	HepG2	liver:	n/a	chr7:111411619-111411630
44	CEBPB	chr7:111367991-111368348	K562	blood:	n/a	chr7:111368176-111368187
45	CEBPB	chr7:111403348-111403903	H1-hESC	embryonic stem cell:	n/a	n/a
46	CEBPB	chr7:111375721-111376020	HepG2	liver:	n/a	chr7:111375805-111375816
47	CEBPB	chr7:111403655-111403862	HepG2	liver:	n/a	n/a
48	CEBPB	chr7:111389434-111389511	H1-hESC	embryonic stem cell:	n/a	chr7:111389478-111389489
49	CEBPB	chr7:111367048-111367642	K562	blood:	n/a	chr7:111367217-111367228
50	CEBPB	chr7:111411483-111412004	H1-hESC	embryonic stem cell:	n/a	chr7:111411619-111411630

(count:976 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:111366042-111366092	PFSK-1	brain:	n/a
2	chr7:111429705-111429755	AG09319	gingival:	n/a
3	chr7:111411453-111411503	SKMC	muscle:	n/a
4	chr7:111368367-111368417	Hela-S3	cervix:	n/a
5	chr7:111411453-111411503	K562	blood:	n/a
6	chr7:111380914-111380964	GM06990	blood:	n/a
7	chr7:111366042-111366092	AG09309	skin:	n/a
8	chr7:111368651-111368701	HAEpiC	amniotic membrane:	n/a
9	chr7:111381500-111381550	AG04450	lung:	fetal
10	chr7:111382084-111382134	AG04449	skin:	fetal
11	chr7:111411453-111411503	HL-60	blood:	n/a
12	chr7:111425428-111425478	GM12878	blood:	n/a
13	chr7:111368367-111368417	U87	brain:	n/a
14	chr7:111380914-111380964	ProgFib	skin:	n/a
15	chr7:111367979-111368029	HCF	heart:	n/a
16	chr7:111368367-111368417	NB4	blood:	n/a
17	chr7:111396894-111396944	ovcar-3	ovarian:	n/a
18	chr7:111368512-111368562	HMEC	breast:	n/a
19	chr7:111430583-111430633	SK-N-SH	brain:	n/a
20	chr7:111425428-111425478	HRCEpiC	kidney:	n/a
21	chr7:111429705-111429755	Hepatocyte	liver:	n/a
22	chr7:111382084-111382134	AG09309	skin:	n/a
23	chr7:111366042-111366092	A549	lung:	n/a
24	chr7:111367979-111368029	HRPEpiC	eye:	n/a
25	chr7:111425428-111425478	AG09309	skin:	n/a
26	chr7:111430583-111430633	IMR90	lung:	fetal
27	chr7:111382084-111382134	HRPEpiC	eye:	n/a
28	chr7:111382084-111382134	HRCEpiC	kidney:	n/a
29	chr7:111368651-111368701	K562	blood:	n/a
30	chr7:111370856-111370906	SAEC	small airway:	n/a
31	chr7:111381500-111381550	GM19239	blood:	n/a
32	chr7:111381500-111381550	K562	blood:	n/a
33	chr7:111380914-111380964	HUVEC	blood vessel:	n/a
34	chr7:111370856-111370906	HCM	heart:	n/a
35	chr7:111368651-111368701	GM12891	blood:	n/a
36	chr7:111368847-111368897	T-47D	breast:	n/a
37	chr7:111368512-111368562	Hela-S3	cervix:	n/a
38	chr7:111375789-111375839	MCF-7	breast:	n/a
39	chr7:111382084-111382134	MCF10A-Er-Src	breast:	n/a
40	chr7:111368651-111368701	HCF	heart:	n/a
41	chr7:111366042-111366092	NHDF-neo	bronchial:	n/a
42	chr7:111429705-111429755	PFSK-1	brain:	n/a
43	chr7:111368847-111368897	NHDF-neo	bronchial:	n/a
44	chr7:111370856-111370906	AG04449	skin:	fetal
45	chr7:111381500-111381550	HCF	heart:	n/a
46	chr7:111370856-111370906	HEEpiC	esophagus:	n/a
47	chr7:111370856-111370906	CMK	blood:	n/a
48	chr7:111375789-111375839	ProgFib	skin:	n/a
49	chr7:111375789-111375839	HNPCEpiC	eye:	n/a
50	chr7:111375789-111375839	SK-N-MC	brain:	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr7:111403351..111403858-chr7:111493448..111494292,2	MCF-7	breast:
2	chr7:110969503..110970311-chr7:111375483..111376413,3	K562	blood:
3	chr7:111392617..111395439-chr7:112089708..112091981,2	MCF-7	breast:
4	chr7:111366447..111368624-chr7:111371924..111374736,3	K562	blood:
5	chr7:111406292..111408372-chr7:111436038..111438457,2	K562	blood:
6	chr7:111375968..111377581-chr7:111379996..111381507,2	K562	blood:
7	chr7:111433541..111435284-chr7:111437283..111439571,2	K562	blood:
8	chr7:108253284..108254285-chr7:111375491..111376402,6	K562	blood:
9	chr7:111405257..111407356-chr7:111411492..111413150,2	K562	blood:
10	chr7:111381701..111382455-chr7:111391667..111392480,3	K562	blood:
11	chr7:111395713..111398642-chr7:111400360..111402475,3	K562	blood:
12	chr7:111381701..111382455-chr7:111391667..111392480,3	K562	blood:
13	chr7:111381542..111382436-chr7:112135847..112136539,2	MCF-7	breast:
14	chr7:111381750..111382252-chr7:112134617..112135164,2	MCF-7	breast:
15	chr16:79635953..79636564-chr7:111391936..111392917,2	MCF-7	breast:
16	chr7:111200196..111203350-chr7:111375147..111377525,3	K562	blood:
17	chr7:110969454..110970228-chr7:111375556..111376647,3	MCF-7	breast:
18	chr7:111441157..111443026-chr7:111452220..111453748,2	K562	blood:
19	chr7:111377015..111379761-chr7:111385528..111388506,2	K562	blood:
20	chr7:111403379..111404358-chr7:112051159..112051887,3	MCF-7	breast:
21	chr7:111398842..111402033-chr7:111404296..111409080,5	K562	blood:
22	chr7:111201065..111203980-chr7:111370429..111371993,2	K562	blood:
23	chr7:111361301..111364499-chr7:111364641..111368279,4	K562	blood:
24	chr7:111416869..111418813-chr7:112089430..112091135,2	MCF-7	breast:
25	chr7:111420094..111422342-chr7:111422479..111424124,2	K562	blood:
26	chr7:111379760..111381665-chr7:112090051..112092325,2	MCF-7	breast:
27	chr7:111389145..111391485-chr7:111396422..111399124,2	K562	blood:
28	chr7:111406292..111408372-chr7:111436038..111438457,2	K562	blood:
29	chr7:111402998..111403979-chr7:111495040..111496257,7	MCF-7	breast:
30	chr7:111441157..111443495-chr7:111452248..111454661,2	K562	blood:
31	chr7:111395713..111398642-chr7:111400360..111402475,3	K562	blood:
32	chr7:111362538..111364445-chr7:111371666..111373265,2	K562	blood:
33	chr7:111381965..111384735-chr7:111387573..111389766,2	K562	blood:
34	chr7:111402781..111405209-chr7:111495007..111496917,24	MCF-7	breast:
35	chr7:111403001..111404142-chr7:111493354..111494316,8	MCF-7	breast:
36	chr7:111381523..111382478-chr7:112135251..112136853,11	K562	blood:
37	chr7:111348035..111349791-chr7:111351253..111353124,2	MCF-7	breast:
38	chr7:111424885..111427263-chr7:111430297..111431978,2	MCF-7	breast:
39	chr7:111456789..111459447-chr7:111459893..111461688,2	MCF-7	breast:
40	chr7:110941321..110943443-chr7:111373654..111375242,2	K562	blood:
41	chr7:111397423..111399750-chr7:112089184..112092163,2	MCF-7	breast:
42	chr7:111403064..111403857-chr7:111440015..111440911,2	MCF-7	breast:
43	chr7:111375601..111376325-chr7:111392437..111393038,2	K562	blood:
44	chr7:111381582..111382456-chr7:112054719..112055629,4	K562	blood:
45	chr7:111392109..111392933-chr7:112186478..112187415,3	K562	blood:
46	chr7:111388076..111390645-chr7:111397624..111399991,2	K562	blood:
47	chr7:111381392..111383489-chr7:112089378..112092065,2	K562	blood:
48	chr7:111402564..111405279-chr7:111424581..111426807,2	MCF-7	breast:
49	chr7:110953570..110955733-chr7:111376151..111377847,2	MCF-7	breast:
50	chr7:111399040..111402198-chr7:111403102..111407043,6	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF277-1	chr7:111448561-111448669	NONHSAT122774
2	lnc-ZNF277-1	chr7:111448572-111448669	ENSG00000225572.1

No data

Variant related genes	Relation type
DOCK4-AS1	TF binding region
DOCK4	TF binding region
DOCK4-AS1	CpG island
DOCK4	CpG island
ENSG00000128512	chromatin interactions
ENSG00000184903	chromatin interactions
ENSG00000198839	chromatin interactions
ENSG00000006652	chromatin interactions

Extended variants
information (count: 4107 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:4107 , 50 per page) page: 1 2 3 4 5 6 7 ... 83

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs538448546	chr7:111337145-111337146	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs557260098	chr7:111337146-111337147	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs575429748	chr7:111337157-111337158	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs542635558	chr7:111337180-111337181	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs573872053	chr7:111337188-111337189	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs560905147	chr7:111337222-111337223	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs573001333	chr7:111337259-111337260	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs540372147	chr7:111337265-111337266	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs565222499	chr7:111337267-111337268	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs181804388	chr7:111337284-111337285	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs550873087	chr7:111337326-111337327	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs541172087	chr7:111337348-111337349	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs373283563	chr7:111337367-111337368	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs559466735	chr7:111337409-111337410	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs116290745	chr7:111337445-111337446	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs376597567	chr7:111337448-111337449	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs185197379	chr7:111337453-111337454	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs188105940	chr7:111337500-111337501	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs34587256	chr7:111337540-111337541	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs181362239	chr7:111337572-111337573	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs571241369	chr7:111337585-111337586	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs538857629	chr7:111337592-111337593	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs556851596	chr7:111337702-111337703	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs116696332	chr7:111337715-111337716	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs186324655	chr7:111337790-111337791	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs79635435	chr7:111337794-111337795	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs545004142	chr7:111337818-111337819	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs536093505	chr7:111337878-111337879	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs554437592	chr7:111337897-111337898	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs572938911	chr7:111337911-111337912	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs540217016	chr7:111337912-111337913	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs563108814	chr7:111337942-111337943	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs565405349	chr7:111337978-111337979	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs191628671	chr7:111337982-111337983	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs118062889	chr7:111337991-111337992	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs562901271	chr7:111337997-111337998	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs530421199	chr7:111338034-111338035	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs118017951	chr7:111338037-111338038	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs367696484	chr7:111338160-111338161	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs147262290	chr7:111338162-111338163	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs550165590	chr7:111338164-111338165	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs546599477	chr7:111338174-111338175	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs148321587	chr7:111338199-111338200	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs540863013	chr7:111338201-111338202	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs559566062	chr7:111338216-111338217	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs568362871	chr7:111338343-111338344	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs536026693	chr7:111338365-111338366	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs554474361	chr7:111338395-111338396	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs183541703	chr7:111338400-111338401	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs371143995	chr7:111338414-111338415	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:91)

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
Autism	20841430	CNVD
Cancer	20164919	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD
Glioblastoma multiforme	20824129	CNVD
Chordoma	21215367	CNVD
Pancreatic cancer	17952125	CNVD
T-cell lymphomas	22341440	CNVD

Chromatin state (count:1690 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:111337000-111338800	Enhancers	HMEC	breast
2	chr7:111337400-111337800	Enhancers	Placenta	Placenta
3	chr7:111337400-111338000	Enhancers	NHEK	skin
4	chr7:111337400-111338200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
5	chr7:111337400-111338200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr7:111346800-111347000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr7:111349200-111349600	Enhancers	iPS-18 Cell Line	embryonic stem cell
8	chr7:111350800-111352400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr7:111351000-111351400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr7:111351000-111352400	Enhancers	HMEC	breast
11	chr7:111351200-111352400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr7:111351400-111352000	Enhancers	HUVEC	blood vessel
13	chr7:111351600-111352000	Enhancers	Muscle Satellite Cultured Cells	--
14	chr7:111351800-111352200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
15	chr7:111352400-111357000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
16	chr7:111357000-111357600	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
17	chr7:111357200-111357600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
18	chr7:111357600-111358600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
19	chr7:111357800-111358400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
20	chr7:111357800-111368400	Weak transcription	Pancreas	Pancrea
21	chr7:111358600-111359000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
22	chr7:111358600-111359800	Enhancers	HMEC	breast
23	chr7:111359000-111359600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
24	chr7:111359600-111359800	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
25	chr7:111359800-111371800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr7:111362400-111362600	Enhancers	Brain Angular Gyrus	brain
27	chr7:111362600-111370000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
28	chr7:111362600-111372400	Weak transcription	Brain Angular Gyrus	brain
29	chr7:111363000-111418000	Weak transcription	Rectal Smooth Muscle	rectum
30	chr7:111363200-111367400	Weak transcription	HUVEC	blood vessel
31	chr7:111363400-111372800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
32	chr7:111364000-111367400	Weak transcription	Brain Hippocampus Middle	brain
33	chr7:111364000-111367600	Weak transcription	Liver	Liver
34	chr7:111364000-111367600	Weak transcription	Brain Anterior Caudate	brain
35	chr7:111364000-111369800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
36	chr7:111364200-111372000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr7:111364200-111378800	Weak transcription	HepG2	liver
38	chr7:111364400-111367600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
39	chr7:111364400-111367600	Weak transcription	Adipose Nuclei	Adipose
40	chr7:111364400-111368200	Weak transcription	Fetal Lung	lung
41	chr7:111364400-111368200	Weak transcription	Lung	lung
42	chr7:111364400-111368600	Weak transcription	Fetal Muscle Leg	muscle
43	chr7:111364400-111371400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
44	chr7:111364400-111376400	Weak transcription	Right Atrium	heart
45	chr7:111364600-111367200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
46	chr7:111364600-111368400	Weak transcription	Left Ventricle	heart
47	chr7:111365400-111368200	Weak transcription	Brain Germinal Matrix	brain
48	chr7:111365800-111372000	Weak transcription	Brain Cingulate Gyrus	brain
49	chr7:111365800-111375600	Weak transcription	Osteobl	bone
50	chr7:111366000-111367800	Weak transcription	Cortex derived primary cultured neurospheres	brain

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