Variant report

Variant	nsv1019347
Chromosome Location	chr7:153734323-153934210
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:973)
CpG islands
(count:1344)
Chromatin interactive
region (count:24)
LncRNA
region (count:10)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:973 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:153769096-153769295	HepG2	liver:	n/a	n/a
2	BATF	chr7:153751061-153751258	GM12878	blood:	n/a	n/a
3	BATF	chr7:153736892-153737175	GM12878	blood:	n/a	chr7:153737026-153737037
4	BCL3	chr7:153859914-153860158	GM12878	blood:	n/a	n/a
5	BCL3	chr7:153854455-153854692	GM12878	blood:	n/a	n/a
6	BCL3	chr7:153859636-153859901	GM12878	blood:	n/a	n/a
7	BCL3	chr7:153859712-153860043	GM12878	blood:	n/a	n/a
8	BHLHE40	chr7:153901718-153901857	K562	blood:	n/a	n/a
9	BHLHE40	chr7:153768947-153769197	K562	blood:	n/a	n/a
10	CBX3	chr7:153768886-153769284	K562	blood:	n/a	chr7:153769006-153769017
11	CEBPB	chr7:153768984-153769330	Hela-S3	cervix:	n/a	n/a
12	CEBPB	chr7:153806768-153806977	K562	blood:	n/a	chr7:153806818-153806835
13	CEBPB	chr7:153917537-153917667	A549	lung:	n/a	n/a
14	CEBPB	chr7:153768945-153769311	K562	blood:	n/a	n/a
15	CEBPB	chr7:153768992-153769253	H1-hESC	embryonic stem cell:	n/a	n/a
16	CEBPB	chr7:153769001-153769334	K562	blood:	n/a	n/a
17	CEBPB	chr7:153823300-153823439	K562	blood:	n/a	chr7:153823347-153823358 chr7:153823348-153823359
18	CEBPB	chr7:153895628-153895876	K562	blood:	n/a	chr7:153895737-153895748
19	CEBPB	chr7:153895591-153895896	HepG2	liver:	n/a	chr7:153895737-153895748
20	CEBPB	chr7:153823261-153823486	HepG2	liver:	n/a	chr7:153823347-153823358 chr7:153823348-153823359
21	CEBPB	chr7:153769011-153769323	HepG2	liver:	n/a	n/a
22	CEBPB	chr7:153900214-153900460	K562	blood:	n/a	n/a
23	CEBPB	chr7:153933911-153934111	H1-hESC	embryonic stem cell:	n/a	chr7:153934002-153934013 chr7:153934000-153934011 chr7:153934002-153934011 chr7:153934000-153934013
24	CEBPB	chr7:153933837-153934154	HepG2	liver:	n/a	chr7:153934002-153934013 chr7:153934000-153934011 chr7:153934002-153934011 chr7:153934000-153934013
25	CEBPB	chr7:153932068-153932361	HepG2	liver:	n/a	chr7:153932183-153932194
26	CEBPB	chr7:153900228-153900489	H1-hESC	embryonic stem cell:	n/a	n/a
27	CEBPB	chr7:153895607-153895846	A549	lung:	n/a	chr7:153895737-153895748
28	CEBPB	chr7:153933875-153934163	K562	blood:	n/a	chr7:153934002-153934013 chr7:153934000-153934011 chr7:153934002-153934011 chr7:153934000-153934013
29	CEBPB	chr7:153878077-153878254	H1-hESC	embryonic stem cell:	n/a	n/a
30	CEBPB	chr7:153823260-153823495	A549	lung:	n/a	chr7:153823347-153823358 chr7:153823348-153823359
31	CEBPB	chr7:153769050-153769261	K562	blood:	n/a	n/a
32	CEBPB	chr7:153895591-153895914	IMR90	lung:	n/a	chr7:153895737-153895748
33	CEBPB	chr7:153895576-153895929	K562	blood:	n/a	chr7:153895737-153895748
34	CEBPB	chr7:153895562-153896455	H1-hESC	embryonic stem cell:	n/a	chr7:153895737-153895748
35	CEBPB	chr7:153932029-153932283	IMR90	lung:	n/a	chr7:153932183-153932194
36	CEBPB	chr7:153769004-153769316	A549	lung:	n/a	n/a
37	CEBPB	chr7:153932139-153932277	H1-hESC	embryonic stem cell:	n/a	chr7:153932183-153932194
38	CHD2	chr7:153881450-153881639	H1-hESC	embryonic stem cell:	n/a	n/a
39	CHD2	chr7:153877999-153878147	K562	blood:	n/a	n/a
40	CTCF	chr7:153745464-153745498	HepG2	liver:	n/a	chr7:153745478-153745487
41	CTCF	chr7:153737017-153737156	SK-N-SH_RA	brain:	n/a	chr7:153737082-153737095 chr7:153737075-153737096 chr7:153737081-153737097 chr7:153737080-153737098
42	CTCF	chr7:153846343-153846508	Hela-S3	cervix:	n/a	chr7:153846474-153846487
43	CTCF	chr7:153815164-153815327	GM12878	blood:	n/a	chr7:153815248-153815269 chr7:153815253-153815271
44	CTCF	chr7:153819893-153819978	LNCaP	prostate:	n/a	n/a
45	CTCF	chr7:153769040-153769190	HL-60	blood:	n/a	chr7:153769130-153769151 chr7:153769129-153769145 chr7:153769128-153769146 chr7:153769131-153769144 chr7:153769133-153769143
46	CTCF	chr7:153792445-153792521	GM12891	blood:	n/a	n/a
47	CTCF	chr7:153751863-153752022	Spleen_OC	spleen:	n/a	n/a
48	CTCF	chr7:153792168-153792225	GM19238	blood:	n/a	n/a
49	CTCF	chr7:153815104-153815354	MCF-7	breast:	n/a	chr7:153815248-153815269 chr7:153815253-153815271
50	CTCF	chr7:153748494-153748709	Kidney_OC	kidney:	n/a	chr7:153748578-153748591 chr7:153748618-153748631

(count:1344 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:153756537-153756587	ovcar-3	ovarian:	n/a
2	chr7:153757646-153757696	NB4	blood:	n/a
3	chr7:153756537-153756587	ovcar-3	ovarian:	n/a
4	chr7:153757646-153757696	NB4	blood:	n/a
5	chr7:153749759-153749809	SK-N-MC	brain:	n/a
6	chr7:153756537-153756587	HNPCEpiC	eye:	n/a
7	chr7:153744840-153744890	MCF10A-Er-Src	breast:	n/a
8	chr7:153756532-153756582	HCPEpiC	choroid plexus:	n/a
9	chr7:153759202-153759252	IMR90	lung:	fetal
10	chr7:153757172-153757222	HL-60	blood:	n/a
11	chr7:153749206-153749256	HRE	kidney:	n/a
12	chr7:153749738-153749788	HCM	heart:	n/a
13	chr7:153751298-153751348	NT2-D1	testis:	n/a
14	chr7:153756532-153756582	GM12891	blood:	n/a
15	chr7:153756537-153756587	U87	brain:	n/a
16	chr7:153744840-153744890	HCPEpiC	choroid plexus:	n/a
17	chr7:153749756-153749806	K562	blood:	n/a
18	chr7:153749756-153749806	NT2-D1	testis:	n/a
19	chr7:153897058-153897108	PrEC	prostate:	n/a
20	chr7:153749206-153749256	GM12892	blood:	n/a
21	chr7:153757172-153757222	Hela-S3	cervix:	n/a
22	chr7:153757172-153757222	HRCEpiC	kidney:	n/a
23	chr7:153749756-153749806	ECC-1	luminal epithelium:	n/a
24	chr7:153749756-153749806	NH-A	brain:	n/a
25	chr7:153749736-153749786	AG04450	lung:	fetal
26	chr7:153749756-153749806	AG04449	skin:	fetal
27	chr7:153757172-153757222	HepG2	liver:	n/a
28	chr7:153757646-153757696	HCT-116	colon:	n/a
29	chr7:153749206-153749256	Jurkat	blood:	n/a
30	chr7:153749756-153749806	AG10803	skin:	n/a
31	chr7:153749206-153749256	AG09319	gingival:	n/a
32	chr7:153748370-153748420	NB4	blood:	n/a
33	chr7:153749964-153750014	ECC-1	luminal epithelium:	n/a
34	chr7:153751298-153751348	CMK	blood:	n/a
35	chr7:153751298-153751348	HPAEpiC	pulmonary alveolar:	n/a
36	chr7:153749964-153750014	Caco-2	colon:	n/a
37	chr7:153756537-153756587	NT2-D1	testis:	n/a
38	chr7:153759202-153759252	HL-60	blood:	n/a
39	chr7:153748370-153748420	H1-hESC	embryonic stem cell:	embryo
40	chr7:153757646-153757696	ProgFib	skin:	n/a
41	chr7:153749759-153749809	HepG2	liver:	n/a
42	chr7:153748818-153748868	PANC-1	pancreas:	n/a
43	chr7:153749964-153750014	RPTEC	kidney:	n/a
44	chr7:153749206-153749256	HEK293	kidney:	embryo
45	chr7:153750421-153750471	MCF10A-Er-Src	breast:	n/a
46	chr7:153749964-153750014	HMEC	breast:	n/a
47	chr7:153757172-153757222	HIPEpiC	eye:	n/a
48	chr7:153748818-153748868	HepG2	liver:	n/a
49	chr7:153749738-153749788	SK-N-MC	brain:	n/a
50	chr7:153750421-153750471	Hepatocyte	liver:	n/a

(count:24 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:153934074..153935744-chr7:153939516..153941778,2	K562	blood:
2	chr7:153872328..153875063-chr7:153876704..153878326,2	K562	blood:
3	chr7:153888225..153889762-chr7:153890722..153892836,2	K562	blood:
4	chr7:153879491..153881734-chr7:153882763..153885706,2	K562	blood:
5	chr7:153899540..153901152-chr7:153909031..153911232,2	MCF-7	breast:
6	chr7:153905453..153907471-chr7:153907886..153910553,2	K562	blood:
7	chr7:153871685..153875063-chr7:153876215..153878326,3	K562	blood:
8	chr7:153871685..153875063-chr7:153876215..153878326,3	K562	blood:
9	chr7:153927635..153929753-chr7:153929796..153932613,2	K562	blood:
10	chr7:153883122..153885530-chr7:153906500..153908289,2	K562	blood:
11	chr7:153879491..153881734-chr7:153882763..153885706,2	K562	blood:
12	chr7:153872328..153875063-chr7:153876704..153878326,2	K562	blood:
13	chr7:153887119..153889725-chr7:153891256..153892836,2	K562	blood:
14	chr7:153905453..153907471-chr7:153907886..153910553,2	K562	blood:
15	chr7:153768676..153769197-chr7:154535648..154536557,2	MCF-7	breast:
16	chr7:153876278..153878269-chr7:154060111..154062732,2	K562	blood:
17	chr7:153899540..153901152-chr7:153909031..153911232,2	MCF-7	breast:
18	chr7:149639335..149639849-chr7:153850966..153851836,2	MCF-7	breast:
19	chr7:153768624..153769652-chr7:154200741..154201698,3	K562	blood:
20	chr7:153883122..153885530-chr7:153906500..153908289,2	K562	blood:
21	chr7:153888225..153889762-chr7:153890722..153892836,2	K562	blood:
22	chr7:153887119..153889725-chr7:153891256..153892836,2	K562	blood:
23	chr7:149699024..149700856-chr7:153788710..153791500,2	K562	blood:
24	chr7:153927635..153929753-chr7:153929796..153932613,2	K562	blood:

(count:10 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PAXIP1-3	chr7:153735519-153735689	ENSG00000203335.3
2	lnc-PAXIP1-3	chr7:153752662-153753010	NONHSAT124310
3	lnc-PAXIP1-3	chr7:153752662-153753010	NONHSAT124311
4	lnc-PAXIP1-3	chr7:153756456-153756554	NONHSAT124311
5	lnc-PAXIP1-2	chr7:153789286-153790002	ENSG00000233363.1
6	lnc-PAXIP1-3	chr7:153756456-153756554	NONHSAT124310
7	lnc-PAXIP1-3	chr7:153754518-153754712	ENSG00000203335.3
8	lnc-PAXIP1-3	chr7:153759996-153760004	NONHSAT124310
9	lnc-PAXIP1-2	chr7:153790802-153793128	ENSG00000233363.1
10	lnc-PAXIP1-3	chr7:153758062-153758183	NONHSAT124311

No data

Variant related genes	Relation type
DPP6	TF binding region
ENSG00000203335	TF binding region
ENSG00000270114	TF binding region
ENSG00000233363	TF binding region
DPP6	CpG island
ENSG00000203335	CpG island
ENSG00000270114	CpG island
ENSG00000233363	CpG island

Extended variants
information (count: 4821 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:4821 , 50 per page) page: 1 2 3 4 5 6 7 ... 97

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs528704045	chr7:153735609-153735610	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
2	rs546928712	chr7:153735621-153735622	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
3	rs557310971	chr7:153736311-153736312	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs200691157	chr7:153736334-153736335	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs539521778	chr7:153736371-153736372	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs201464130	chr7:153736383-153736384	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs192938028	chr7:153736414-153736415	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs576589553	chr7:153736419-153736420	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs112489181	chr7:153736423-153736424	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs541224500	chr7:153736433-153736434	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs71243487	chr7:153736441-153736442	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs557814209	chr7:153736623-153736624	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs113879687	chr7:153736934-153736935	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs199524854	chr7:153736975-153736976	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs574659826	chr7:153737023-153737024	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs541786967	chr7:153737066-153737067	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs146297438	chr7:153737095-153737096	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs2533773	chr7:153737099-153737100	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs575325873	chr7:153737196-153737197	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs545872395	chr7:153737239-153737240	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs564172864	chr7:153737277-153737278	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs528239190	chr7:153737327-153737328	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs547160301	chr7:153737348-153737349	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs562181668	chr7:153737386-153737387	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs529571830	chr7:153737399-153737400	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs151213448	chr7:153737441-153737442	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs139206594	chr7:153737453-153737454	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs185177003	chr7:153737454-153737455	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs149919433	chr7:153737468-153737469	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs145026616	chr7:153737475-153737476	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs149054359	chr7:153737477-153737478	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs535184260	chr7:153737479-153737480	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs557238636	chr7:153738202-153738203	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs550839702	chr7:153744872-153744873	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
35	rs62485567	chr7:153744875-153744876	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
36	rs569162008	chr7:153744877-153744878	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
37	rs200989370	chr7:153745021-153745022	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs539757316	chr7:153745191-153745192	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs551069438	chr7:153745206-153745207	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs199826252	chr7:153745212-153745213	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs200458365	chr7:153745431-153745432	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs151259356	chr7:153747188-153747189	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs548546294	chr7:153747452-153747453	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
44	rs34718012	chr7:153747467-153747468	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
45	rs566943564	chr7:153747484-153747485	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
46	rs182782172	chr7:153747505-153747506	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
47	rs2628696	chr7:153747526-153747527	Bivalent Enhancer	CpG island	1 gene(s)	Overlapped CNVs	n/a
48	rs549471325	chr7:153747561-153747562	Bivalent Enhancer	CpG island	1 gene(s)	Overlapped CNVs	n/a
49	rs374428258	chr7:153747587-153747588	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
50	rs571484731	chr7:153747595-153747596	Bivalent Enhancer	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
Wilms tumour	21544195	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
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
lymphocytic leukemia	21291569	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16573809	CNVD
Medulloblastoma	16783165	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Hodgkin''s lymphoma	18179710	CNVD
Breast cancer	17603634	CNVD
Urothelial carcinoma	18382360	CNVD
Myelodysplastic syndrome	17634407	CNVD
Multiple myeloma	16461302	CNVD
Neuroblastoma	18923191	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Acute myeloid leukemia	16864856	CNVD
Autism	20808228	CNVD
Ovarian cancer	21720365	CNVD
Lobular carcinoma	20920651	CNVD
Long-qt syndrome	20920651	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Sudden cardiac death	19188705	CNVD
renal disease	17924346	CNVD
Myelofibrosis	22110671	CNVD
Nasopharyngeal cancer	20548289	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Amyotrophic lateral sclerosis	20685689	CNVD
Autism	19546859	CNVD
Schizophrenia	19546859	CNVD
Tourette syndrome	19546859	CNVD
Breast cancer	21509527	CNVD
Pancreatic cancer	17952125	CNVD
Congenital anomalies of the kidney and urinary tract	20605837	CNVD
Breast cancer	22522925	CNVD
Autism	22102821	CNVD
small cell lung cancer	20016488	CNVD
Autism	22495309	CNVD
early-passage human iPS cells	21368824	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Chordoma	21215367	CNVD
Cancer	21215367	CNVD
Schizophrenia	23813976	CNVD

Chromatin state (count:369 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:153747400-153747600	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
2	chr7:153748000-153748200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr7:153748000-153748200	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
4	chr7:153748000-153748200	Enhancers	Stomach Smooth Muscle	stomach
5	chr7:153748000-153748400	Enhancers	Rectal Smooth Muscle	rectum
6	chr7:153748000-153748600	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
7	chr7:153748000-153748800	Active TSS	H1 Cell Line	embryonic stem cell
8	chr7:153748000-153748800	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr7:153748000-153749600	Active TSS	iPS-20b Cell Line	embryonic stem cell
10	chr7:153748000-153749600	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
11	chr7:153748000-153750800	Active TSS	Brain Anterior Caudate	brain
12	chr7:153748000-153751400	Active TSS	Brain Inferior Temporal Lobe	brain
13	chr7:153748200-153748400	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
14	chr7:153748200-153748400	Flanking Bivalent TSS/Enh	Colon Smooth Muscle	Colon
15	chr7:153748200-153748400	Bivalent Enhancer	Fetal Muscle Leg	muscle
16	chr7:153748200-153748400	Bivalent Enhancer	Lung	lung
17	chr7:153748200-153748400	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
18	chr7:153748200-153748600	Active TSS	HUES64 Cell Line	embryonic stem cell
19	chr7:153748200-153748800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
20	chr7:153748200-153749000	Enhancers	Adipose Nuclei	Adipose
21	chr7:153748200-153749000	Active TSS	Brain Angular Gyrus	brain
22	chr7:153748200-153749000	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
23	chr7:153748200-153749600	Active TSS	Brain Germinal Matrix	brain
24	chr7:153748200-153749800	Active TSS	HUES48 Cell Line	embryonic stem cell
25	chr7:153748200-153750000	Active TSS	Stomach Smooth Muscle	stomach
26	chr7:153748200-153750400	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
27	chr7:153748200-153750400	Active TSS	Brain Hippocampus Middle	brain
28	chr7:153748200-153750600	Active TSS	iPS-15b Cell Line	embryonic stem cell
29	chr7:153748200-153750800	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
30	chr7:153748200-153751600	Active TSS	Fetal Brain Female	brain
31	chr7:153748400-153748800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
32	chr7:153748400-153749000	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
33	chr7:153748400-153750400	Active TSS	Brain Cingulate Gyrus	brain
34	chr7:153748400-153750600	Active TSS	H9 Cell Line	embryonic stem cell
35	chr7:153748400-153750800	Active TSS	Cortex derived primary cultured neurospheres	brain
36	chr7:153748400-153750800	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
37	chr7:153748600-153749400	Active TSS	iPS-18 Cell Line	embryonic stem cell
38	chr7:153748600-153750800	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
39	chr7:153748800-153749000	Bivalent/Poised TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
40	chr7:153748800-153749000	Flanking Bivalent TSS/Enh	Fetal Adrenal Gland	Adrenal Gland
41	chr7:153748800-153749000	Flanking Bivalent TSS/Enh	Fetal Muscle Trunk	muscle
42	chr7:153748800-153749000	Bivalent/Poised TSS	Fetal Muscle Leg	muscle
43	chr7:153748800-153749400	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
44	chr7:153748800-153749600	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
45	chr7:153748800-153750000	Bivalent/Poised TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr7:153748800-153750400	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
47	chr7:153748800-153750400	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr7:153748800-153750400	Bivalent/Poised TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
49	chr7:153748800-153750400	Active TSS	Breast Myoepithelial Primary Cells	Breast
50	chr7:153748800-153750800	Bivalent/Poised TSS	H1 Cell Line	embryonic stem cell

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