Variant report

Variant	nsv889248
Chromosome Location	chr7:140754785-140809205
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:140797283-140797500	K562	blood:	n/a	n/a
2	ATF1	chr7:140783114-140783483	K562	blood:	n/a	n/a
3	ATF2	chr7:140771918-140772666	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr7:140772054-140772660	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr7:140770901-140771578	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr7:140771124-140771317	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr7:140794499-140794757	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr7:140772218-140772709	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr7:140771799-140771866	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr7:140772932-140773267	H1-hESC	embryonic stem cell:	n/a	n/a
11	BCL11A	chr7:140783178-140783368	GM12878	blood:	n/a	chr7:140783269-140783278
12	BRCA1	chr7:140771130-140771330	H1-hESC	embryonic stem cell:	n/a	n/a
13	CEBPB	chr7:140771024-140771365	H1-hESC	embryonic stem cell:	n/a	n/a
14	CEBPB	chr7:140757884-140758103	HepG2	liver:	n/a	chr7:140757960-140757971 chr7:140758004-140758015
15	CEBPB	chr7:140793563-140793763	HepG2	liver:	n/a	chr7:140793641-140793652
16	CEBPB	chr7:140773164-140773178	H1-hESC	embryonic stem cell:	n/a	n/a
17	CEBPB	chr7:140769110-140769224	A549	lung:	n/a	n/a
18	CHD1	chr7:140771075-140771448	H1-hESC	embryonic stem cell:	n/a	n/a
19	CHD1	chr7:140771650-140772883	H1-hESC	embryonic stem cell:	n/a	n/a
20	CHD1	chr7:140773196-140774773	H1-hESC	embryonic stem cell:	n/a	chr7:140774314-140774324 chr7:140774533-140774540 chr7:140773808-140773818 chr7:140773821-140773831 chr7:140774306-140774316
21	CHD2	chr7:140771739-140771957	H1-hESC	embryonic stem cell:	n/a	n/a
22	CHD2	chr7:140771134-140771232	GM12878	blood:	n/a	n/a
23	CHD2	chr7:140797260-140797271	H1-hESC	embryonic stem cell:	n/a	n/a
24	CHD2	chr7:140773076-140773266	H1-hESC	embryonic stem cell:	n/a	n/a
25	CHD2	chr7:140771038-140771538	H1-hESC	embryonic stem cell:	n/a	n/a
26	CHD2	chr7:140773895-140774066	H1-hESC	embryonic stem cell:	n/a	n/a
27	CREB1	chr7:140772292-140772565	A549	lung:	n/a	chr7:140772367-140772380
28	CTBP2	chr7:140772433-140774683	H1-hESC	embryonic stem cell:	n/a	n/a
29	CTCF	chr7:140774024-140774110	H1-hESC	embryonic stem cell:	n/a	n/a
30	CTCF	chr7:140783282-140783355	Gliobla	brain:	n/a	n/a
31	CTCF	chr7:140771140-140771290	A549	lung:	n/a	chr7:140771226-140771234 chr7:140771221-140771239 chr7:140771223-140771244 chr7:140771222-140771238
32	CTCF	chr7:140774240-140774390	SK-N-SH_RA	brain:	n/a	n/a
33	CTCF	chr7:140770840-140770990	HRE	kidney:	n/a	n/a
34	CTCF	chr7:140771120-140771270	HA-sp	spinal cord:	n/a	chr7:140771226-140771234 chr7:140771221-140771239 chr7:140771223-140771244 chr7:140771222-140771238
35	CTCF	chr7:140771105-140771318	GM12892	blood:	n/a	chr7:140771226-140771234 chr7:140771221-140771239 chr7:140771223-140771244 chr7:140771222-140771238
36	CTCF	chr7:140783210-140783321	Lung_OC	lung:	n/a	n/a
37	CTCF	chr7:140771100-140771250	NHEK	skin:	n/a	chr7:140771226-140771234 chr7:140771221-140771239 chr7:140771223-140771244 chr7:140771222-140771238
38	CTCF	chr7:140771092-140771368	Medullo	brain:	n/a	chr7:140771226-140771234 chr7:140771221-140771239 chr7:140771223-140771244 chr7:140771222-140771238
39	CTCF	chr7:140771150-140771284	Spleen_OC	spleen:	n/a	chr7:140771226-140771234 chr7:140771221-140771239 chr7:140771223-140771244 chr7:140771222-140771238
40	CTCF	chr7:140771260-140771410	HCM	heart:	n/a	n/a
41	CTCF	chr7:140772340-140772490	AG09319	gingival:	n/a	n/a
42	CTCF	chr7:140774020-140774170	SK-N-SH_RA	brain:	n/a	n/a
43	CTCF	chr7:140771160-140771310	HMF	breast:	n/a	chr7:140771226-140771234 chr7:140771221-140771239 chr7:140771223-140771244 chr7:140771222-140771238
44	CTCF	chr7:140771160-140771310	BE2_C	brain:	n/a	chr7:140771226-140771234 chr7:140771221-140771239 chr7:140771223-140771244 chr7:140771222-140771238
45	CTCF	chr7:140771184-140771285	HepG2	liver:	n/a	chr7:140771226-140771234 chr7:140771221-140771239 chr7:140771223-140771244 chr7:140771222-140771238
46	CTCF	chr7:140771148-140771291	NHEK	skin:	n/a	chr7:140771226-140771234 chr7:140771221-140771239 chr7:140771223-140771244 chr7:140771222-140771238
47	CTCF	chr7:140771180-140771330	RPTEC	kidney:	n/a	chr7:140771226-140771234 chr7:140771221-140771239 chr7:140771223-140771244 chr7:140771222-140771238
48	CTCF	chr7:140771100-140771250	GM12875	blood:	n/a	chr7:140771226-140771234 chr7:140771221-140771239 chr7:140771223-140771244 chr7:140771222-140771238
49	CTCF	chr7:140790060-140790210	GM06990	blood:	n/a	n/a
50	CTCF	chr7:140771200-140771350	GM12873	blood:	n/a	chr7:140771226-140771234 chr7:140771221-140771239 chr7:140771223-140771244 chr7:140771222-140771238

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:140771827-140771877	A549	lung:	n/a
2	chr7:140773578-140773628	GM12892	blood:	n/a
3	chr7:140771827-140771877	A549	lung:	n/a
4	chr7:140773578-140773628	GM12892	blood:	n/a
5	chr7:140802949-140802999	HRE	kidney:	n/a
6	chr7:140772932-140772982	MCF-7	breast:	n/a
7	chr7:140771827-140771877	HCPEpiC	choroid plexus:	n/a
8	chr7:140772932-140772982	HCT-116	colon:	n/a
9	chr7:140773578-140773628	PFSK-1	brain:	n/a
10	chr7:140773905-140773955	GM19239	blood:	n/a
11	chr7:140773736-140773786	H1-hESC	embryonic stem cell:	embryo
12	chr7:140774161-140774211	BJ	skin:	n/a
13	chr7:140776653-140776703	GM06990	blood:	n/a
14	chr7:140774104-140774154	ovcar-3	ovarian:	n/a
15	chr7:140773736-140773786	HNPCEpiC	eye:	n/a
16	chr7:140771419-140771469	U87	brain:	n/a
17	chr7:140802949-140802999	ProgFib	skin:	n/a
18	chr7:140773422-140773472	H1-hESC	embryonic stem cell:	embryo
19	chr7:140772457-140772507	NHBE	bronchial:	n/a
20	chr7:140770260-140770310	BE2_C	brain:	n/a
21	chr7:140773905-140773955	BE2_C	brain:	n/a
22	chr7:140772457-140772507	T-47D	breast:	n/a
23	chr7:140774714-140774764	Hela-S3	cervix:	n/a
24	chr7:140770260-140770310	BJ	skin:	n/a
25	chr7:140773905-140773955	AoSMC	blood vessel:	n/a
26	chr7:140773736-140773786	SK-N-SH_RA	brain:	n/a
27	chr7:140802949-140802999	HCPEpiC	choroid plexus:	n/a
28	chr7:140802949-140802999	Caco-2	colon:	n/a
29	chr7:140776653-140776703	HL-60	blood:	n/a
30	chr7:140772932-140772982	PFSK-1	brain:	n/a
31	chr7:140774161-140774211	AG04450	lung:	fetal
32	chr7:140774104-140774154	PANC-1	pancreas:	n/a
33	chr7:140802949-140802999	AG04450	lung:	fetal
34	chr7:140774714-140774764	Jurkat	blood:	n/a
35	chr7:140771827-140771877	HCM	heart:	n/a
36	chr7:140771827-140771877	Hela-S3	cervix:	n/a
37	chr7:140802949-140802999	AG09309	skin:	n/a
38	chr7:140771419-140771469	SK-N-SH_RA	brain:	n/a
39	chr7:140770260-140770310	CMK	blood:	n/a
40	chr7:140802949-140802999	HPAEpiC	pulmonary alveolar:	n/a
41	chr7:140773905-140773955	PrEC	prostate:	n/a
42	chr7:140776653-140776703	GM19239	blood:	n/a
43	chr7:140771827-140771877	T-47D	breast:	n/a
44	chr7:140772457-140772507	HEEpiC	esophagus:	n/a
45	chr7:140772810-140772860	HCT-116	colon:	n/a
46	chr7:140772932-140772982	HCPEpiC	choroid plexus:	n/a
47	chr7:140802949-140802999	RPTEC	kidney:	n/a
48	chr7:140774104-140774154	T-47D	breast:	n/a
49	chr7:140774104-140774154	PFSK-1	brain:	n/a
50	chr7:140773422-140773472	AG09309	skin:	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:140713242..140716757-chr7:140770540..140776348,9	MCF-7	breast:
2	chr7:140756685..140759591-chr7:140773952..140776899,2	K562	blood:
3	chr7:140772460..140775375-chr7:140783158..140785995,3	MCF-7	breast:
4	chr7:140713041..140715567-chr7:140788354..140789900,2	K562	blood:
5	chr7:140772523..140774077-chr7:140786831..140788416,2	MCF-7	breast:
6	chr7:140772357..140774530-chr7:140777823..140780428,2	K562	blood:
7	chr7:140770669..140771613-chr7:140919796..140920746,4	MCF-7	breast:
8	chr7:140713014..140715287-chr7:140752870..140754963,2	K562	blood:
9	chr7:140791037..140792664-chr7:140793260..140795969,2	K562	blood:
10	chr7:140790828..140792569-chr7:140797247..140798946,2	MCF-7	breast:
11	chr7:140767357..140769762-chr7:140774657..140776517,2	K562	blood:
12	chr7:140711595..140714521-chr7:140757199..140759357,2	K562	blood:
13	chr7:140770653..140771598-chr7:140931029..140931808,2	MCF-7	breast:
14	chr7:140726381..140728137-chr7:140770810..140773677,2	MCF-7	breast:
15	chr7:140776160..140778796-chr7:140827028..140829508,2	MCF-7	breast:
16	chr7:140774318..140775981-chr7:140800025..140801816,2	MCF-7	breast:
17	chr7:140757803..140760583-chr7:140769573..140772261,2	K562	blood:
18	chr7:140774318..140775981-chr7:140800025..140801816,2	MCF-7	breast:
19	chr7:140791037..140792664-chr7:140793260..140795969,2	K562	blood:
20	chr7:140712784..140717043-chr7:140770770..140775163,8	MCF-7	breast:
21	chr7:140790828..140792569-chr7:140797247..140798946,2	MCF-7	breast:
22	chr7:140757803..140760583-chr7:140769573..140772261,2	K562	blood:
23	chr7:140767357..140769762-chr7:140774657..140776517,2	K562	blood:
24	chr7:140770942..140773181-chr7:140930215..140932967,2	MCF-7	breast:
25	chr7:140714581..140715382-chr7:140772383..140773295,2	MCF-7	breast:
26	chr7:140772309..140775530-chr7:140801888..140805201,4	MCF-7	breast:
27	chr7:140774135..140775705-chr7:140796756..140798922,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MRPS33-1	chr7:140773120-140773406	XLOC_006623
2	lnc-MRPS33-1	chr7:140774650-140774682	XLOC_006623

Variant related genes	Relation type
TMEM178B	TF binding region
TMEM178B	CpG island
ENSG00000090263	chromatin interactions
ENSG00000261115	chromatin interactions

Extended variants
information (count: 1419 )
Associated
traits (count: 101 )

Variant overlapped rSNPs/rCNVs (count:1419 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11764061	chr7:140754785-140754786	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs192328635	chr7:140754817-140754818	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs569403354	chr7:140754837-140754838	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs572252568	chr7:140754890-140754891	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs536758247	chr7:140754919-140754920	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs547114978	chr7:140754925-140754926	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs117597946	chr7:140754945-140754946	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs574173498	chr7:140754951-140754952	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs535289996	chr7:140754956-140754957	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs558045708	chr7:140754987-140754988	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs535989878	chr7:140755041-140755042	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs138042212	chr7:140755042-140755043	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs184776561	chr7:140755070-140755071	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs545416608	chr7:140755127-140755128	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs149532196	chr7:140755141-140755142	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs575650797	chr7:140755145-140755146	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs188120757	chr7:140755149-140755150	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs143199785	chr7:140755166-140755167	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs12112332	chr7:140755170-140755171	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs529065457	chr7:140755235-140755236	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs547220540	chr7:140755252-140755253	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs559222368	chr7:140755259-140755260	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs490810	chr7:140755264-140755265	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
24	rs148298131	chr7:140755275-140755276	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs569313947	chr7:140755301-140755302	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs536860620	chr7:140755332-140755333	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs537121262	chr7:140755367-140755368	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs548820736	chr7:140755391-140755392	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs141990002	chr7:140755400-140755401	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs534884380	chr7:140755430-140755431	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs374518847	chr7:140755449-140755450	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs200701799	chr7:140755450-140755451	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs10259285	chr7:140755492-140755493	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs146304791	chr7:140755536-140755537	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs193068473	chr7:140755554-140755555	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs139572777	chr7:140755564-140755565	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs575569753	chr7:140755593-140755594	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs543044863	chr7:140755605-140755606	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs184714600	chr7:140755633-140755634	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs573336140	chr7:140755642-140755643	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs540819885	chr7:140755658-140755659	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs494520	chr7:140755683-140755684	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
43	rs565216335	chr7:140755684-140755685	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs149707859	chr7:140755722-140755723	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs398006619	chr7:140755728-140755729	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs533013330	chr7:140755738-140755739	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs189431057	chr7:140755811-140755812	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs544924680	chr7:140755842-140755843	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs73498965	chr7:140755848-140755849	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs530409339	chr7:140755884-140755885	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:101)

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
Wilms tumour	21544195	CNVD
T-cell prolymphocytic leukemia	19278963	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
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
Chronic myeloid leukemia	21384125	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
lymphocytic leukemia	21291569	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16573809	CNVD
Medulloblastoma	16783165	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Melanoma	19188590	CNVD
Glioblastoma multiforme	18628472	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Malignant melanoma	17260012	CNVD
Coffin-Siris syndrome	21572526	CNVD
Papillary thyroid carcinoma	21436994	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Hodgkin''s lymphoma	18179710	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	16272173	CNVD
Myxofibrosarcoma	16751306	CNVD
Stuttering	21108403	CNVD
Breast cancer	17603634	CNVD
Urothelial carcinoma	18382360	CNVD
Myelodysplastic syndrome	17634407	CNVD
Cancer	21129771	CNVD
Myelofibrosis	22110671	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
T-cell acute lymphoblastic leukemia	16673021	CNVD
Cancer	21183584	CNVD
Intracranial ependymoma	16609018	CNVD
Non-small cell lung cancer	21829676	CNVD
Developmental delay	19490664	CNVD
Pancreatitis	20877625	CNVD
Multiple myeloma	16461302	CNVD
Neuroblastoma	18923191	CNVD
Medulloblastoma	16968546	CNVD
Pilocytic astrocytoma	18408760	CNVD
Idiopathic chronic pancreatitis	19584086	CNVD
Low-grade astrocytoma	19016743	CNVD
Pediatric low-grade astrocytoma	19016743	CNVD
Acute lymphoblastic leukemia	17315016	CNVD
Gastric cancer	16891809	CNVD
Cancer	17440070	CNVD
Astrocytoma	18398503	CNVD
Melanoma	19671679	CNVD
Lung adenocarcinoma	19525976	CNVD
Lung cancer	19525976	CNVD
Breast cancer	17133270	CNVD
Schizophrenia	17646849	CNVD
Glioblastoma multiforme	21525872	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:859 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:140753800-140757800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr7:140757200-140757800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr7:140767000-140768000	Active TSS	ES-I3 Cell Line	embryonic stem cell
4	chr7:140767600-140767800	Active TSS	HUES64 Cell Line	embryonic stem cell
5	chr7:140767600-140768000	Active TSS	HUES6 Cell Line	embryonic stem cell
6	chr7:140767800-140768000	Flanking Bivalent TSS/Enh	HUES64 Cell Line	embryonic stem cell
7	chr7:140767800-140768000	Active TSS	iPS-15b Cell Line	embryonic stem cell
8	chr7:140767800-140768000	Active TSS	K562	blood
9	chr7:140767800-140768200	Enhancers	H9 Cell Line	embryonic stem cell
10	chr7:140768000-140768200	Enhancers	H1 Cell Line	embryonic stem cell
11	chr7:140768000-140768200	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
12	chr7:140768000-140768200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
13	chr7:140768000-140768200	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr7:140768000-140768200	Flanking Active TSS	K562	blood
15	chr7:140768200-140768400	Enhancers	K562	blood
16	chr7:140768200-140770800	Weak transcription	H9 Cell Line	embryonic stem cell
17	chr7:140769000-140771000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
18	chr7:140770400-140770600	Enhancers	H1 Cell Line	embryonic stem cell
19	chr7:140770600-140770800	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
20	chr7:140770600-140770800	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
21	chr7:140770600-140770800	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
22	chr7:140770600-140770800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
23	chr7:140770600-140770800	Enhancers	Cortex derived primary cultured neurospheres	brain
24	chr7:140770600-140770800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
25	chr7:140770600-140770800	Enhancers	Brain Inferior Temporal Lobe	brain
26	chr7:140770600-140771000	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
27	chr7:140770600-140771000	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
28	chr7:140770600-140771000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
29	chr7:140770600-140771000	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
30	chr7:140770600-140777000	Active TSS	Fetal Brain Female	brain
31	chr7:140770800-140771000	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
32	chr7:140770800-140771000	Enhancers	H9 Cell Line	embryonic stem cell
33	chr7:140770800-140771000	Flanking Bivalent TSS/Enh	HUES6 Cell Line	embryonic stem cell
34	chr7:140770800-140771000	Flanking Bivalent TSS/Enh	iPS-18 Cell Line	embryonic stem cell
35	chr7:140770800-140771000	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
36	chr7:140770800-140771000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
37	chr7:140770800-140771000	Enhancers	Brain Hippocampus Middle	brain
38	chr7:140770800-140771000	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
39	chr7:140770800-140771000	Enhancers	Colon Smooth Muscle	Colon
40	chr7:140770800-140771000	Enhancers	Fetal Brain Male	brain
41	chr7:140770800-140771000	Bivalent Enhancer	Fetal Lung	lung
42	chr7:140770800-140771200	Flanking Bivalent TSS/Enh	H1 Cell Line	embryonic stem cell
43	chr7:140770800-140771200	Flanking Bivalent TSS/Enh	iPS-20b Cell Line	embryonic stem cell
44	chr7:140770800-140771200	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
45	chr7:140770800-140771200	Bivalent/Poised TSS	Stomach Smooth Muscle	stomach
46	chr7:140770800-140771800	Bivalent Enhancer	Fetal Intestine Large	intestine
47	chr7:140770800-140772000	Bivalent/Poised TSS	Duodenum Smooth Muscle	Duodenum
48	chr7:140770800-140772200	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
49	chr7:140770800-140772400	Active TSS	Brain Germinal Matrix	brain
50	chr7:140770800-140774600	Active TSS	Brain Anterior Caudate	brain

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