Variant report

Variant	esv2465998
Chromosome Location	chr7:153664757-153844588
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	chr7:153769096-153769295	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	chr7:153686222-153686486	GM12878	blood:	n/a	n/a
5	BCL3	chr7:153686171-153686487	GM12878	blood:	n/a	n/a
6	BHLHE40	chr7:153671731-153672005	HepG2	liver:	n/a	n/a
7	BHLHE40	chr7:153768947-153769197	K562	blood:	n/a	n/a
8	CBX3	chr7:153768886-153769284	K562	blood:	n/a	chr7:153769006-153769017
9	CEBPB	chr7:153769011-153769323	HepG2	liver:	n/a	n/a
10	CEBPB	chr7:153823260-153823495	A549	lung:	n/a	chr7:153823347-153823358 chr7:153823348-153823359
11	CEBPB	chr7:153823261-153823486	HepG2	liver:	n/a	chr7:153823347-153823358 chr7:153823348-153823359
12	CEBPB	chr7:153769004-153769316	A549	lung:	n/a	n/a
13	CEBPB	chr7:153768945-153769311	K562	blood:	n/a	n/a
14	CEBPB	chr7:153823300-153823439	K562	blood:	n/a	chr7:153823347-153823358 chr7:153823348-153823359
15	CEBPB	chr7:153768992-153769253	H1-hESC	embryonic stem cell:	n/a	n/a
16	CEBPB	chr7:153708406-153708655	A549	lung:	n/a	chr7:153708509-153708518 chr7:153708509-153708518 chr7:153708509-153708518 chr7:153708507-153708518 chr7:153708509-153708518
17	CEBPB	chr7:153703491-153703685	HepG2	liver:	n/a	chr7:153703626-153703637 chr7:153703628-153703637
18	CEBPB	chr7:153708328-153708611	HepG2	liver:	n/a	chr7:153708509-153708518 chr7:153708509-153708518 chr7:153708509-153708518 chr7:153708507-153708518 chr7:153708509-153708518
19	CEBPB	chr7:153769050-153769261	K562	blood:	n/a	n/a
20	CEBPB	chr7:153769001-153769334	K562	blood:	n/a	n/a
21	CEBPB	chr7:153806768-153806977	K562	blood:	n/a	chr7:153806818-153806835
22	CEBPB	chr7:153671722-153671982	HepG2	liver:	n/a	n/a
23	CEBPB	chr7:153708400-153708682	K562	blood:	n/a	chr7:153708509-153708518 chr7:153708509-153708518 chr7:153708509-153708518 chr7:153708507-153708518 chr7:153708509-153708518
24	CEBPB	chr7:153768984-153769330	Hela-S3	cervix:	n/a	n/a
25	CTCF	chr7:153829845-153830004	Kidney_OC	kidney:	n/a	chr7:153829858-153829867 chr7:153829855-153829873
26	CTCF	chr7:153815182-153815309	Fibrobl	skin:	n/a	chr7:153815248-153815269 chr7:153815253-153815271
27	CTCF	chr7:153736944-153737228	Gliobla	brain:	n/a	chr7:153737082-153737095 chr7:153737075-153737096 chr7:153737081-153737097 chr7:153737080-153737098
28	CTCF	chr7:153829770-153829996	Hela-S3	cervix:	n/a	chr7:153829858-153829867 chr7:153829855-153829873
29	CTCF	chr7:153736958-153737196	GM12892	blood:	n/a	chr7:153737082-153737095 chr7:153737075-153737096 chr7:153737081-153737097 chr7:153737080-153737098
30	CTCF	chr7:153768997-153769278	Medullo	brain:	n/a	chr7:153769130-153769151 chr7:153769129-153769145 chr7:153769128-153769146 chr7:153769131-153769144 chr7:153769133-153769143
31	CTCF	chr7:153769060-153769210	A549	lung:	n/a	chr7:153769130-153769151 chr7:153769129-153769145 chr7:153769128-153769146 chr7:153769131-153769144 chr7:153769133-153769143
32	CTCF	chr7:153687023-153687199	LNCaP	prostate:	n/a	chr7:153687148-153687161 chr7:153687149-153687159 chr7:153687141-153687162 chr7:153687095-153687108 chr7:153687146-153687164 chr7:153687152-153687161 chr7:153687093-153687111
33	CTCF	chr7:153815114-153815362	K562	blood:	n/a	chr7:153815248-153815269 chr7:153815253-153815271
34	CTCF	chr7:153792441-153792547	A549	lung:	n/a	n/a
35	CTCF	chr7:153751907-153751987	LNCaP	prostate:	n/a	n/a
36	CTCF	chr7:153821194-153821271	LNCaP	prostate:	n/a	n/a
37	CTCF	chr7:153737000-153737150	GM12867	blood:	n/a	chr7:153737082-153737095 chr7:153737075-153737096 chr7:153737081-153737097 chr7:153737080-153737098
38	CTCF	chr7:153769020-153769170	NHEK	skin:	n/a	chr7:153769130-153769151 chr7:153769129-153769145 chr7:153769128-153769146 chr7:153769131-153769144 chr7:153769133-153769143
39	CTCF	chr7:153736960-153737110	WERI-Rb-1	eye:	n/a	chr7:153737082-153737095 chr7:153737075-153737096 chr7:153737081-153737097 chr7:153737080-153737098
40	CTCF	chr7:153712700-153712850	K562	blood:	n/a	n/a
41	CTCF	chr7:153792428-153792650	K562	blood:	n/a	n/a
42	CTCF	chr7:153815119-153815351	Hela-S3	cervix:	n/a	chr7:153815248-153815269 chr7:153815253-153815271
43	CTCF	chr7:153687030-153687158	Gliobla	brain:	n/a	chr7:153687095-153687108 chr7:153687093-153687111
44	CTCF	chr7:153751863-153752022	Spleen_OC	spleen:	n/a	n/a
45	CTCF	chr7:153769062-153769198	HUVEC	blood vessel:	n/a	chr7:153769130-153769151 chr7:153769129-153769145 chr7:153769128-153769146 chr7:153769131-153769144 chr7:153769133-153769143
46	CTCF	chr7:153792432-153792578	LNCaP	prostate:	n/a	n/a
47	CTCF	chr7:153815156-153815324	MCF-7	breast:	n/a	chr7:153815248-153815269 chr7:153815253-153815271
48	CTCF	chr7:153736979-153737209	HUVEC	blood vessel:	n/a	chr7:153737082-153737095 chr7:153737075-153737096 chr7:153737081-153737097 chr7:153737080-153737098
49	CTCF	chr7:153769020-153769170	HMF	breast:	n/a	chr7:153769130-153769151 chr7:153769129-153769145 chr7:153769128-153769146 chr7:153769131-153769144 chr7:153769133-153769143
50	CTCF	chr7:153736960-153737110	GM12865	blood:	n/a	chr7:153737082-153737095 chr7:153737075-153737096 chr7:153737081-153737097 chr7:153737080-153737098

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:153757646-153757696	GM06990	blood:	n/a
2	chr7:153749206-153749256	MCF-7	breast:	n/a
3	chr7:153757646-153757696	GM06990	blood:	n/a
4	chr7:153749206-153749256	MCF-7	breast:	n/a
5	chr7:153749964-153750014	A549	lung:	n/a
6	chr7:153752727-153752777	HCT-116	colon:	n/a
7	chr7:153757172-153757222	HRE	kidney:	n/a
8	chr7:153759202-153759252	HNPCEpiC	eye:	n/a
9	chr7:153749964-153750014	AG09319	gingival:	n/a
10	chr7:153755533-153755583	NB4	blood:	n/a
11	chr7:153747525-153747575	HMEC	breast:	n/a
12	chr7:153748370-153748420	PrEC	prostate:	n/a
13	chr7:153749756-153749806	H1-hESC	embryonic stem cell:	embryo
14	chr7:153755533-153755583	Caco-2	colon:	n/a
15	chr7:153752727-153752777	AG04449	skin:	fetal
16	chr7:153748818-153748868	HCM	heart:	n/a
17	chr7:153749206-153749256	HCM	heart:	n/a
18	chr7:153759349-153759399	Jurkat	blood:	n/a
19	chr7:153755533-153755583	K562	blood:	n/a
20	chr7:153752727-153752777	BJ	skin:	n/a
21	chr7:153749964-153750014	HMEC	breast:	n/a
22	chr7:153749736-153749786	NT2-D1	testis:	n/a
23	chr7:153759349-153759399	HCF	heart:	n/a
24	chr7:153759349-153759399	T-47D	breast:	n/a
25	chr7:153752727-153752777	PANC-1	pancreas:	n/a
26	chr7:153744840-153744890	BE2_C	brain:	n/a
27	chr7:153749736-153749786	HPAEpiC	pulmonary alveolar:	n/a
28	chr7:153749738-153749788	GM06990	blood:	n/a
29	chr7:153756537-153756587	LNCaP	prostate:	n/a
30	chr7:153749964-153750014	HCPEpiC	choroid plexus:	n/a
31	chr7:153749736-153749786	PANC-1	pancreas:	n/a
32	chr7:153749964-153750014	HCF	heart:	n/a
33	chr7:153749756-153749806	AG04449	skin:	fetal
34	chr7:153751298-153751348	HIPEpiC	eye:	n/a
35	chr7:153759349-153759399	AG04449	skin:	fetal
36	chr7:153752727-153752777	SK-N-SH_RA	brain:	n/a
37	chr7:153750421-153750471	HPAEpiC	pulmonary alveolar:	n/a
38	chr7:153755533-153755583	BE2_C	brain:	n/a
39	chr7:153748370-153748420	CMK	blood:	n/a
40	chr7:153748818-153748868	HAEpiC	amniotic membrane:	n/a
41	chr7:153757646-153757696	ovcar-3	ovarian:	n/a
42	chr7:153752727-153752777	SKMC	muscle:	n/a
43	chr7:153749756-153749806	HCT-116	colon:	n/a
44	chr7:153757172-153757222	AoSMC	blood vessel:	n/a
45	chr7:153756532-153756582	PFSK-1	brain:	n/a
46	chr7:153751298-153751348	HNPCEpiC	eye:	n/a
47	chr7:153749759-153749809	K562	blood:	n/a
48	chr7:153757646-153757696	SKMC	muscle:	n/a
49	chr7:153748370-153748420	PFSK-1	brain:	n/a
50	chr7:153759349-153759399	CMK	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:153768624..153769652-chr7:154200741..154201698,3	K562	blood:
2	chr7:149699024..149700856-chr7:153788710..153791500,2	K562	blood:
3	chr7:153768676..153769197-chr7:154535648..154536557,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PAXIP1-3	chr7:153758062-153758183	NONHSAT124311
2	lnc-PAXIP1-3	chr7:153752662-153753010	NONHSAT124311
3	lnc-PAXIP1-3	chr7:153756456-153756554	NONHSAT124310
4	lnc-PAXIP1-2	chr7:153790802-153793128	ENSG00000233363.1
5	lnc-PAXIP1-3	chr7:153754518-153754712	ENSG00000203335.3
6	lnc-PAXIP1-3	chr7:153723665-153723775	ENSG00000203335.3
7	lnc-PAXIP1-3	chr7:153724009-153724133	ENSG00000203335.3
8	lnc-PAXIP1-3	chr7:153759996-153760004	NONHSAT124310
9	lnc-PAXIP1-3	chr7:153723372-153723775	ENSG00000203335.3
10	lnc-PAXIP1-2	chr7:153789286-153790002	ENSG00000233363.1
11	lnc-PAXIP1-3	chr7:153752662-153753010	NONHSAT124310
12	lnc-PAXIP1-3	chr7:153721094-153721199	ENSG00000203335.3
13	lnc-PAXIP1-3	chr7:153724009-153724131	ENSG00000203335.3
14	lnc-PAXIP1-3	chr7:153756456-153756554	NONHSAT124311
15	lnc-PAXIP1-3	chr7:153735519-153735689	ENSG00000203335.3

Variant related genes	Relation type
DPP6	TF binding region
ENSG00000203335	TF binding region
ENSG00000270114	TF binding region
ENSG00000226509	TF binding region
ENSG00000233363	TF binding region
DPP6	CpG island
ENSG00000203335	CpG island
ENSG00000270114	CpG island
ENSG00000226509	CpG island
ENSG00000233363	CpG island

Extended variants
information (count: 3774 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:3774 , 50 per page) page: 1 2 3 4 5 6 7 ... 76

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs573931433	chr7:153668893-153668894	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs544588260	chr7:153668908-153668909	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs144300623	chr7:153669475-153669476	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs541527812	chr7:153671807-153671808	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs559558520	chr7:153671819-153671820	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs530132449	chr7:153671820-153671821	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs148083346	chr7:153671843-153671844	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs10236251	chr7:153671870-153671871	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs531106592	chr7:153671879-153671880	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs370708258	chr7:153671884-153671885	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs570727753	chr7:153671907-153671908	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs186004804	chr7:153671911-153671912	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs39150	chr7:153671940-153671941	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs565623768	chr7:153671943-153671944	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs374120806	chr7:153671957-153671958	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs554604119	chr7:153671977-153671978	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs555747600	chr7:153672035-153672036	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs537354650	chr7:153672044-153672045	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs39149	chr7:153672048-153672049	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs191166017	chr7:153672054-153672055	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs540844029	chr7:153672146-153672147	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs559829853	chr7:153672161-153672162	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs574827162	chr7:153672163-153672164	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs78694955	chr7:153672172-153672173	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs114015370	chr7:153672188-153672189	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs569260096	chr7:153685602-153685603	Bivalent Enhancer Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
27	rs116511594	chr7:153685624-153685625	Bivalent Enhancer Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
28	rs199601665	chr7:153685635-153685636	Bivalent Enhancer Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
29	rs540818121	chr7:153685636-153685637	Bivalent Enhancer Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
30	rs553148631	chr7:153685688-153685689	Bivalent Enhancer Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
31	rs2907723	chr7:153685698-153685699	Bivalent Enhancer Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
32	rs574481369	chr7:153685701-153685702	Bivalent Enhancer Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
33	rs541522207	chr7:153685728-153685729	Bivalent Enhancer Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
34	rs563312730	chr7:153685737-153685738	Bivalent Enhancer Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
35	rs530399215	chr7:153685771-153685772	Bivalent Enhancer Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
36	rs561817981	chr7:153686804-153686805	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
37	rs2533614	chr7:153686824-153686825	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
38	rs143677079	chr7:153686839-153686840	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
39	rs191045783	chr7:153686843-153686844	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
40	rs562653432	chr7:153686848-153686849	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
41	rs11767297	chr7:153686862-153686863	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
42	rs551867704	chr7:153686866-153686867	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
43	rs560496765	chr7:153686867-153686868	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
44	rs527666326	chr7:153686881-153686882	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
45	rs534952910	chr7:153686883-153686884	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
46	rs549685406	chr7:153686904-153686905	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
47	rs182393655	chr7:153686908-153686909	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
48	rs375495201	chr7:153686910-153686911	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
49	rs188326461	chr7:153686920-153686921	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
50	rs550110532	chr7:153686921-153686922	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
Chordoma	21215367	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
Cancer	21215367	CNVD
Schizophrenia	23813976	CNVD

Chromatin state (count:170 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:153671800-153672200	Enhancers	HepG2	liver
2	chr7:153685600-153685800	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
3	chr7:153685600-153685800	Flanking Bivalent TSS/Enh	Fetal Muscle Trunk	muscle
4	chr7:153686800-153687000	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
5	chr7:153702200-153705200	Enhancers	Fetal Muscle Leg	muscle
6	chr7:153705200-153708000	Weak transcription	Fetal Muscle Leg	muscle
7	chr7:153706600-153708800	Enhancers	Skeletal Muscle Male	skeletal muscle
8	chr7:153708000-153708600	Enhancers	Fetal Muscle Leg	muscle
9	chr7:153708200-153708600	Enhancers	Skeletal Muscle Female	skeletal muscle
10	chr7:153708400-153708600	Enhancers	Psoas Muscle	Psoas
11	chr7:153708600-153711000	Weak transcription	Skeletal Muscle Female	skeletal muscle
12	chr7:153708600-153717800	Weak transcription	Fetal Muscle Leg	muscle
13	chr7:153708800-153710000	Weak transcription	Psoas Muscle	Psoas
14	chr7:153710000-153710400	Enhancers	Psoas Muscle	Psoas
15	chr7:153711000-153711200	Enhancers	Skeletal Muscle Female	skeletal muscle
16	chr7:153717800-153718600	Enhancers	Fetal Muscle Leg	muscle
17	chr7:153718600-153719600	Weak transcription	Fetal Muscle Leg	muscle
18	chr7:153719600-153719800	Enhancers	Fetal Muscle Leg	muscle
19	chr7:153719800-153727000	Weak transcription	Fetal Muscle Leg	muscle
20	chr7:153723600-153723800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
21	chr7:153723800-153725000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
22	chr7:153725000-153725400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
23	chr7:153726400-153727600	Enhancers	Fetal Muscle Trunk	muscle
24	chr7:153727000-153729200	Enhancers	Fetal Muscle Leg	muscle
25	chr7:153747400-153747600	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
26	chr7:153748000-153748200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
27	chr7:153748000-153748200	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
28	chr7:153748000-153748200	Enhancers	Stomach Smooth Muscle	stomach
29	chr7:153748000-153748400	Enhancers	Rectal Smooth Muscle	rectum
30	chr7:153748000-153748600	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
31	chr7:153748000-153748800	Active TSS	H1 Cell Line	embryonic stem cell
32	chr7:153748000-153748800	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
33	chr7:153748000-153749600	Active TSS	iPS-20b Cell Line	embryonic stem cell
34	chr7:153748000-153749600	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
35	chr7:153748000-153750800	Active TSS	Brain Anterior Caudate	brain
36	chr7:153748000-153751400	Active TSS	Brain Inferior Temporal Lobe	brain
37	chr7:153748200-153748400	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
38	chr7:153748200-153748400	Flanking Bivalent TSS/Enh	Colon Smooth Muscle	Colon
39	chr7:153748200-153748400	Bivalent Enhancer	Fetal Muscle Leg	muscle
40	chr7:153748200-153748400	Bivalent Enhancer	Lung	lung
41	chr7:153748200-153748400	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
42	chr7:153748200-153748600	Active TSS	HUES64 Cell Line	embryonic stem cell
43	chr7:153748200-153748800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
44	chr7:153748200-153749000	Enhancers	Adipose Nuclei	Adipose
45	chr7:153748200-153749000	Active TSS	Brain Angular Gyrus	brain
46	chr7:153748200-153749000	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
47	chr7:153748200-153749600	Active TSS	Brain Germinal Matrix	brain
48	chr7:153748200-153749800	Active TSS	HUES48 Cell Line	embryonic stem cell
49	chr7:153748200-153750000	Active TSS	Stomach Smooth Muscle	stomach
50	chr7:153748200-153750400	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell

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