Variant report

Variant	nsv482279
Chromosome Location	chr7:153681785-153883800
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	chr7:153736892-153737175	GM12878	blood:	n/a	chr7:153737026-153737037
3	BATF	chr7:153751061-153751258	GM12878	blood:	n/a	n/a
4	BCL3	chr7:153859914-153860158	GM12878	blood:	n/a	n/a
5	BCL3	chr7:153859636-153859901	GM12878	blood:	n/a	n/a
6	BCL3	chr7:153854455-153854692	GM12878	blood:	n/a	n/a
7	BCL3	chr7:153686222-153686486	GM12878	blood:	n/a	n/a
8	BCL3	chr7:153686171-153686487	GM12878	blood:	n/a	n/a
9	BCL3	chr7:153859712-153860043	GM12878	blood:	n/a	n/a
10	BHLHE40	chr7:153768947-153769197	K562	blood:	n/a	n/a
11	CBX3	chr7:153768886-153769284	K562	blood:	n/a	chr7:153769006-153769017
12	CEBPB	chr7:153823260-153823495	A549	lung:	n/a	chr7:153823347-153823358 chr7:153823348-153823359
13	CEBPB	chr7:153768945-153769311	K562	blood:	n/a	n/a
14	CEBPB	chr7:153768984-153769330	Hela-S3	cervix:	n/a	n/a
15	CEBPB	chr7:153823300-153823439	K562	blood:	n/a	chr7:153823347-153823358 chr7:153823348-153823359
16	CEBPB	chr7:153823261-153823486	HepG2	liver:	n/a	chr7:153823347-153823358 chr7:153823348-153823359
17	CEBPB	chr7:153708406-153708655	A549	lung:	n/a	chr7:153708509-153708518 chr7:153708509-153708518 chr7:153708509-153708518 chr7:153708507-153708518 chr7:153708509-153708518
18	CEBPB	chr7:153708400-153708682	K562	blood:	n/a	chr7:153708509-153708518 chr7:153708509-153708518 chr7:153708509-153708518 chr7:153708507-153708518 chr7:153708509-153708518
19	CEBPB	chr7:153769011-153769323	HepG2	liver:	n/a	n/a
20	CEBPB	chr7:153806768-153806977	K562	blood:	n/a	chr7:153806818-153806835
21	CEBPB	chr7:153769001-153769334	K562	blood:	n/a	n/a
22	CEBPB	chr7:153703491-153703685	HepG2	liver:	n/a	chr7:153703626-153703637 chr7:153703628-153703637
23	CEBPB	chr7:153769050-153769261	K562	blood:	n/a	n/a
24	CEBPB	chr7:153769004-153769316	A549	lung:	n/a	n/a
25	CEBPB	chr7:153768992-153769253	H1-hESC	embryonic stem cell:	n/a	n/a
26	CEBPB	chr7:153878077-153878254	H1-hESC	embryonic stem cell:	n/a	n/a
27	CEBPB	chr7:153708328-153708611	HepG2	liver:	n/a	chr7:153708509-153708518 chr7:153708509-153708518 chr7:153708509-153708518 chr7:153708507-153708518 chr7:153708509-153708518
28	CHD2	chr7:153877999-153878147	K562	blood:	n/a	n/a
29	CHD2	chr7:153881450-153881639	H1-hESC	embryonic stem cell:	n/a	n/a
30	CTCF	chr7:153769080-153769230	BE2_C	brain:	n/a	chr7:153769130-153769151 chr7:153769129-153769145 chr7:153769128-153769146 chr7:153769131-153769144 chr7:153769133-153769143
31	CTCF	chr7:153686950-153687195	MCF-7	breast:	n/a	chr7:153687148-153687161 chr7:153687149-153687159 chr7:153687141-153687162 chr7:153687095-153687108 chr7:153687146-153687164 chr7:153687152-153687161 chr7:153687093-153687111
32	CTCF	chr7:153829770-153829996	Hela-S3	cervix:	n/a	chr7:153829858-153829867 chr7:153829855-153829873
33	CTCF	chr7:153712910-153713130	H1-hESC	embryonic stem cell:	n/a	n/a
34	CTCF	chr7:153687030-153687158	Gliobla	brain:	n/a	chr7:153687095-153687108 chr7:153687093-153687111
35	CTCF	chr7:153769001-153769256	LNCaP	prostate:	n/a	chr7:153769130-153769151 chr7:153769129-153769145 chr7:153769128-153769146 chr7:153769131-153769144 chr7:153769133-153769143
36	CTCF	chr7:153792290-153792576	K562	blood:	n/a	n/a
37	CTCF	chr7:153829787-153830019	LNCaP	prostate:	n/a	chr7:153829858-153829867 chr7:153829855-153829873
38	CTCF	chr7:153736957-153737201	GM19240	blood:	n/a	chr7:153737082-153737095 chr7:153737075-153737096 chr7:153737081-153737097 chr7:153737080-153737098
39	CTCF	chr7:153829680-153829830	HEK293	kidney:	n/a	n/a
40	CTCF	chr7:153736979-153737180	GM19239	blood:	n/a	chr7:153737082-153737095 chr7:153737075-153737096 chr7:153737081-153737097 chr7:153737080-153737098
41	CTCF	chr7:153829798-153829948	GM12878	blood:	n/a	chr7:153829858-153829867 chr7:153829855-153829873
42	CTCF	chr7:153751808-153752066	Medullo	brain:	n/a	n/a
43	CTCF	chr7:153748470-153748737	MCF-7	breast:	n/a	chr7:153748578-153748591 chr7:153748618-153748631
44	CTCF	chr7:153736963-153737245	GM13977	blood:	n/a	chr7:153737082-153737095 chr7:153737075-153737096 chr7:153737081-153737097 chr7:153737080-153737098
45	CTCF	chr7:153769113-153769186	MCF-7	breast:	n/a	chr7:153769130-153769151 chr7:153769129-153769145 chr7:153769128-153769146 chr7:153769131-153769144 chr7:153769133-153769143
46	CTCF	chr7:153815178-153815304	GM19238	blood:	n/a	chr7:153815248-153815269 chr7:153815253-153815271
47	CTCF	chr7:153712920-153713070	NB4	blood:	n/a	n/a
48	CTCF	chr7:153737020-153737170	HRPEpiC	eye:	n/a	chr7:153737082-153737095 chr7:153737075-153737096 chr7:153737081-153737097 chr7:153737080-153737098
49	CTCF	chr7:153846343-153846494	GM19239	blood:	n/a	chr7:153846474-153846487
50	CTCF	chr7:153769020-153769170	NHEK	skin:	n/a	chr7:153769130-153769151 chr7:153769129-153769145 chr7:153769128-153769146 chr7:153769131-153769144 chr7:153769133-153769143

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:153747525-153747575	NHBE	bronchial:	n/a
2	chr7:153749756-153749806	SK-N-SH_RA	brain:	n/a
3	chr7:153747525-153747575	NHBE	bronchial:	n/a
4	chr7:153749756-153749806	SK-N-SH_RA	brain:	n/a
5	chr7:153749759-153749809	AoSMC	blood vessel:	n/a
6	chr7:153756532-153756582	SKMC	muscle:	n/a
7	chr7:153749964-153750014	HL-60	blood:	n/a
8	chr7:153759202-153759252	NH-A	brain:	n/a
9	chr7:153757646-153757696	HAEpiC	amniotic membrane:	n/a
10	chr7:153749738-153749788	HMEC	breast:	n/a
11	chr7:153749756-153749806	HMEC	breast:	n/a
12	chr7:153750421-153750471	PANC-1	pancreas:	n/a
13	chr7:153757646-153757696	HNPCEpiC	eye:	n/a
14	chr7:153749736-153749786	HepG2	liver:	n/a
15	chr7:153751298-153751348	ovcar-3	ovarian:	n/a
16	chr7:153757172-153757222	RPTEC	kidney:	n/a
17	chr7:153749738-153749788	SKMC	muscle:	n/a
18	chr7:153750421-153750471	H1-hESC	embryonic stem cell:	embryo
19	chr7:153748818-153748868	SAEC	small airway:	n/a
20	chr7:153748818-153748868	Hela-S3	cervix:	n/a
21	chr7:153744840-153744890	ECC-1	luminal epithelium:	n/a
22	chr7:153749736-153749786	GM12892	blood:	n/a
23	chr7:153756532-153756582	MCF10A-Er-Src	breast:	n/a
24	chr7:153756532-153756582	A549	lung:	n/a
25	chr7:153881192-153881242	SKMC	muscle:	n/a
26	chr7:153759202-153759252	U87	brain:	n/a
27	chr7:153749964-153750014	HUVEC	blood vessel:	n/a
28	chr7:153756537-153756587	HEEpiC	esophagus:	n/a
29	chr7:153881192-153881242	HPAEpiC	pulmonary alveolar:	n/a
30	chr7:153750421-153750471	GM12892	blood:	n/a
31	chr7:153747525-153747575	AoSMC	blood vessel:	n/a
32	chr7:153752727-153752777	NB4	blood:	n/a
33	chr7:153748818-153748868	HRE	kidney:	n/a
34	chr7:153752727-153752777	AG10803	skin:	n/a
35	chr7:153750421-153750471	CMK	blood:	n/a
36	chr7:153749736-153749786	GM12891	blood:	n/a
37	chr7:153744840-153744890	A549	lung:	n/a
38	chr7:153756532-153756582	RPTEC	kidney:	n/a
39	chr7:153755533-153755583	HRE	kidney:	n/a
40	chr7:153749736-153749786	HCF	heart:	n/a
41	chr7:153881192-153881242	Jurkat	blood:	n/a
42	chr7:153752727-153752777	PFSK-1	brain:	n/a
43	chr7:153748370-153748420	HRPEpiC	eye:	n/a
44	chr7:153752727-153752777	PANC-1	pancreas:	n/a
45	chr7:153747525-153747575	HIPEpiC	eye:	n/a
46	chr7:153744840-153744890	NHDF-neo	bronchial:	n/a
47	chr7:153748370-153748420	Caco-2	colon:	n/a
48	chr7:153755533-153755583	GM06990	blood:	n/a
49	chr7:153749759-153749809	SK-N-MC	brain:	n/a
50	chr7:153750421-153750471	U87	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:153871685..153875063-chr7:153876215..153878326,3	K562	blood:
2	chr7:153872328..153875063-chr7:153876704..153878326,2	K562	blood:
3	chr7:153879491..153881734-chr7:153882763..153885706,2	K562	blood:
4	chr7:153883122..153885530-chr7:153906500..153908289,2	K562	blood:
5	chr7:149639335..149639849-chr7:153850966..153851836,2	MCF-7	breast:
6	chr7:153872328..153875063-chr7:153876704..153878326,2	K562	blood:
7	chr7:149699024..149700856-chr7:153788710..153791500,2	K562	blood:
8	chr7:153876278..153878269-chr7:154060111..154062732,2	K562	blood:
9	chr7:153768676..153769197-chr7:154535648..154536557,2	MCF-7	breast:
10	chr7:153879491..153881734-chr7:153882763..153885706,2	K562	blood:
11	chr7:153768624..153769652-chr7:154200741..154201698,3	K562	blood:
12	chr7:153871685..153875063-chr7:153876215..153878326,3	K562	blood:

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

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: 4775 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:4775 , 50 per page) page: 1 2 3 4 5 6 7 ... 96

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs569260096	chr7:153685602-153685603	Bivalent Enhancer Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
2	rs116511594	chr7:153685624-153685625	Bivalent Enhancer Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
3	rs199601665	chr7:153685635-153685636	Bivalent Enhancer Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
4	rs540818121	chr7:153685636-153685637	Bivalent Enhancer Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
5	rs553148631	chr7:153685688-153685689	Bivalent Enhancer Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
6	rs2907723	chr7:153685698-153685699	Bivalent Enhancer Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
7	rs574481369	chr7:153685701-153685702	Bivalent Enhancer Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
8	rs541522207	chr7:153685728-153685729	Bivalent Enhancer Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
9	rs563312730	chr7:153685737-153685738	Bivalent Enhancer Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
10	rs530399215	chr7:153685771-153685772	Bivalent Enhancer Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
11	rs561817981	chr7:153686804-153686805	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
12	rs2533614	chr7:153686824-153686825	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
13	rs143677079	chr7:153686839-153686840	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
14	rs191045783	chr7:153686843-153686844	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
15	rs562653432	chr7:153686848-153686849	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
16	rs11767297	chr7:153686862-153686863	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
17	rs551867704	chr7:153686866-153686867	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
18	rs560496765	chr7:153686867-153686868	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
19	rs527666326	chr7:153686881-153686882	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
20	rs534952910	chr7:153686883-153686884	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
21	rs549685406	chr7:153686904-153686905	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
22	rs182393655	chr7:153686908-153686909	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
23	rs375495201	chr7:153686910-153686911	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
24	rs188326461	chr7:153686920-153686921	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
25	rs550110532	chr7:153686921-153686922	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
26	rs2907722	chr7:153686955-153686956	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
27	rs553533444	chr7:153686969-153686970	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
28	rs531776112	chr7:153702227-153702228	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs141064542	chr7:153702244-153702245	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs550305162	chr7:153702304-153702305	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs12112278	chr7:153702330-153702331	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs532846188	chr7:153702347-153702348	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs551370379	chr7:153702372-153702373	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs566314877	chr7:153702379-153702380	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs184777560	chr7:153702395-153702396	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs188098467	chr7:153702396-153702397	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs567507945	chr7:153702427-153702428	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs538036788	chr7:153702484-153702485	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs556037695	chr7:153702489-153702490	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs536896629	chr7:153702519-153702520	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs113247995	chr7:153702552-153702553	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs538724416	chr7:153702702-153702703	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs554161860	chr7:153702722-153702723	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs572087946	chr7:153702724-153702725	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs542952035	chr7:153702732-153702733	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs139556874	chr7:153702737-153702738	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs576278904	chr7:153702775-153702776	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs192932757	chr7:153702844-153702845	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs565300363	chr7:153702873-153702874	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs71265441	chr7:153702893-153702894	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
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:325 , 50 per page) page: 1 2 3 4 5 6 7

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

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