Variant report

Variant	nsv831019
Chromosome Location	chr7:66516808-66720485
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1221)
CpG islands
(count:183)
Chromatin interactive
region (count:10)
LncRNA
region (count:0)
Mature miRNA
region (count: 2)
miRNA target
sites (count:0)

(count:1221 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:66641595-66641654	K562	blood:	n/a	n/a
2	ARID3A	chr7:66594175-66594562	HepG2	liver:	n/a	n/a
3	ARID3A	chr7:66631997-66632120	K562	blood:	n/a	n/a
4	ARID3A	chr7:66566033-66566339	K562	blood:	n/a	n/a
5	ARID3A	chr7:66570459-66570758	K562	blood:	n/a	n/a
6	ARID3A	chr7:66690931-66691626	K562	blood:	n/a	n/a
7	ARID3A	chr7:66594120-66594496	K562	blood:	n/a	n/a
8	ARID3A	chr7:66595946-66596068	HepG2	liver:	n/a	n/a
9	ARID3A	chr7:66656128-66656328	K562	blood:	n/a	n/a
10	ARID3A	chr7:66695022-66695111	HepG2	liver:	n/a	n/a
11	ARID3A	chr7:66644119-66644324	K562	blood:	n/a	n/a
12	ARID3A	chr7:66670874-66670983	K562	blood:	n/a	n/a
13	ARID3A	chr7:66586943-66586983	K562	blood:	n/a	n/a
14	ATF1	chr7:66566015-66566333	K562	blood:	n/a	n/a
15	ATF1	chr7:66691319-66691697	K562	blood:	n/a	n/a
16	ATF1	chr7:66594100-66594458	K562	blood:	n/a	n/a
17	ATF2	chr7:66650644-66650864	GM12878	blood:	n/a	n/a
18	ATF2	chr7:66594084-66594536	GM12878	blood:	n/a	n/a
19	ATF2	chr7:66594022-66594509	GM12878	blood:	n/a	n/a
20	ATF3	chr7:66594108-66594487	K562	blood:	n/a	n/a
21	ATF3	chr7:66691349-66691641	K562	blood:	n/a	n/a
22	BATF	chr7:66650660-66651105	GM12878	blood:	n/a	n/a
23	BATF	chr7:66599956-66600326	GM12878	blood:	n/a	chr7:66600114-66600125
24	BATF	chr7:66650720-66651068	GM12878	blood:	n/a	n/a
25	BATF	chr7:66593488-66593762	GM12878	blood:	n/a	n/a
26	BATF	chr7:66594161-66594602	GM12878	blood:	n/a	n/a
27	BATF	chr7:66691481-66691650	GM12878	blood:	n/a	n/a
28	BATF	chr7:66600094-66600339	GM12878	blood:	n/a	chr7:66600114-66600125
29	BATF	chr7:66594062-66594698	GM12878	blood:	n/a	n/a
30	BATF	chr7:66565087-66565356	GM12878	blood:	n/a	n/a
31	BCL11A	chr7:66650672-66651044	GM12878	blood:	n/a	n/a
32	BCL11A	chr7:66650708-66651080	GM12878	blood:	n/a	n/a
33	BCL11A	chr7:66593932-66594470	GM12878	blood:	n/a	n/a
34	BCL11A	chr7:66593952-66594605	GM12878	blood:	n/a	n/a
35	BCL3	chr7:66594144-66594482	GM12878	blood:	n/a	n/a
36	BCL3	chr7:66654178-66654452	GM12878	blood:	n/a	n/a
37	BCL3	chr7:66594042-66594450	GM12878	blood:	n/a	n/a
38	BCL3	chr7:66594039-66594656	A549	lung:	n/a	n/a
39	BCL3	chr7:66594026-66594572	A549	lung:	n/a	n/a
40	BCL3	chr7:66654245-66654539	GM12878	blood:	n/a	n/a
41	BCLAF1	chr7:66594049-66594540	GM12878	blood:	n/a	n/a
42	BCLAF1	chr7:66599905-66600251	GM12878	blood:	n/a	n/a
43	BHLHE40	chr7:66593562-66593577	K562	blood:	n/a	n/a
44	BHLHE40	chr7:66594125-66594330	K562	blood:	n/a	n/a
45	BHLHE40	chr7:66565984-66566323	K562	blood:	n/a	n/a
46	BHLHE40	chr7:66594178-66594448	HepG2	liver:	n/a	n/a
47	BHLHE40	chr7:66594132-66594446	GM12878	blood:	n/a	n/a
48	BRCA1	chr7:66585811-66585829	H1-hESC	embryonic stem cell:	n/a	n/a
49	BRCA1	chr7:66594273-66594414	Hela-S3	cervix:	n/a	n/a
50	CBX3	chr7:66687770-66688093	K562	blood:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:66648157-66648207	PrEC	prostate:	n/a
2	chr7:66648142-66648192	SKMC	muscle:	n/a
3	chr7:66704323-66704373	HCM	heart:	n/a
4	chr7:66704323-66704373	A549	lung:	n/a
5	chr7:66648157-66648207	NB4	blood:	n/a
6	chr7:66648142-66648192	GM12892	blood:	n/a
7	chr7:66648157-66648207	HEK293	kidney:	embryo
8	chr7:66648142-66648192	GM06990	blood:	n/a
9	chr7:66648157-66648207	CMK	blood:	n/a
10	chr7:66648142-66648192	AG09319	gingival:	n/a
11	chr7:66704323-66704373	H1-hESC	embryonic stem cell:	embryo
12	chr7:66704323-66704373	SAEC	small airway:	n/a
13	chr7:66648142-66648192	MCF10A-Er-Src	breast:	n/a
14	chr7:66648157-66648207	H1-hESC	embryonic stem cell:	embryo
15	chr7:66648157-66648207	SAEC	small airway:	n/a
16	chr7:66648142-66648192	NH-A	brain:	n/a
17	chr7:66648142-66648192	HRPEpiC	eye:	n/a
18	chr7:66704323-66704373	BJ	skin:	n/a
19	chr7:66704323-66704373	BE2_C	brain:	n/a
20	chr7:66648142-66648192	HRE	kidney:	n/a
21	chr7:66648142-66648192	H1-hESC	embryonic stem cell:	embryo
22	chr7:66648142-66648192	K562	blood:	n/a
23	chr7:66648157-66648207	HepG2	liver:	n/a
24	chr7:66648157-66648207	NT2-D1	testis:	n/a
25	chr7:66648157-66648207	HPAEpiC	pulmonary alveolar:	n/a
26	chr7:66704323-66704373	K562	blood:	n/a
27	chr7:66704323-66704373	HEEpiC	esophagus:	n/a
28	chr7:66648142-66648192	LNCaP	prostate:	n/a
29	chr7:66704323-66704373	HRE	kidney:	n/a
30	chr7:66648142-66648192	HCM	heart:	n/a
31	chr7:66648142-66648192	HMEC	breast:	n/a
32	chr7:66704323-66704373	RPTEC	kidney:	n/a
33	chr7:66648157-66648207	HCM	heart:	n/a
34	chr7:66704323-66704373	AG09319	gingival:	n/a
35	chr7:66648142-66648192	CMK	blood:	n/a
36	chr7:66648157-66648207	SK-N-SH_RA	brain:	n/a
37	chr7:66648142-66648192	NHDF-neo	bronchial:	n/a
38	chr7:66648157-66648207	MCF-7	breast:	n/a
39	chr7:66648142-66648192	AG10803	skin:	n/a
40	chr7:66648142-66648192	Hela-S3	cervix:	n/a
41	chr7:66648157-66648207	HRCEpiC	kidney:	n/a
42	chr7:66648142-66648192	A549	lung:	n/a
43	chr7:66704323-66704373	ECC-1	luminal epithelium:	n/a
44	chr7:66648157-66648207	LNCaP	prostate:	n/a
45	chr7:66648157-66648207	HNPCEpiC	eye:	n/a
46	chr7:66704323-66704373	HRPEpiC	eye:	n/a
47	chr7:66704323-66704373	HCT-116	colon:	n/a
48	chr7:66648157-66648207	RPTEC	kidney:	n/a
49	chr7:66704323-66704373	Caco-2	colon:	n/a
50	chr7:66648142-66648192	SK-N-SH	brain:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr7:66660286..66662929-chr7:66766070..66767968,2	K562	blood:
2	chr7:66689176..66691737-chr7:66693504..66695940,2	K562	blood:
3	chr7:66641784..66642296-chr7:66836697..66837223,2	MCF-7	breast:
4	chr7:66691444..66695683-chr7:66701018..66704715,3	K562	blood:
5	chr7:66599000..66600532-chr7:66603146..66604759,2	K562	blood:
6	chr7:66204310..66206758-chr7:66515145..66517585,2	MCF-7	breast:
7	chr7:66691444..66695683-chr7:66701018..66704715,3	K562	blood:
8	chr7:66689176..66691737-chr7:66693504..66695940,2	K562	blood:
9	chr7:66508015..66509853-chr7:66521858..66523452,2	K562	blood:
10	chr7:66657820..66660105-chr7:66767390..66769267,2	K562	blood:

No data

miRNA name	Chromosome Location	mirBase accession
hsa-miR-4650-3p	chr7:66579319-66579339	MIMAT0019714
hsa-miR-4650-5p	chr7:66579352-66579370	MIMAT0019713

No data

Variant related genes	Relation type
ENSG00000233383	TF binding region
ENSG00000265024	TF binding region
MIR4650-1	TF binding region
TYW1	TF binding region
ENSG00000233383	CpG island
ENSG00000265024	CpG island
MIR4650-1	CpG island
TYW1	CpG island
ENSG00000243335	chromatin interactions
ENSG00000265024	chromatin interactions
ENSG00000272831	chromatin interactions
ENSG00000067601	chromatin interactions
ENSG00000154710	chromatin interactions
ENSG00000106610	chromatin interactions

Extended variants
information (count: 8292 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:8292 , 50 per page) page: 1 2 3 4 5 6 7 ... 166

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs576523993	chr7:66516852-66516853	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs369580570	chr7:66516877-66516878	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs537260358	chr7:66516910-66516911	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs557564461	chr7:66516922-66516923	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs545684407	chr7:66516981-66516982	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs573871598	chr7:66516990-66516991	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs117713819	chr7:66517033-66517034	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs10273674	chr7:66517049-66517050	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
9	rs572511105	chr7:66517054-66517055	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs193216157	chr7:66517067-66517068	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs564845815	chr7:66517109-66517110	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs12667271	chr7:66517151-66517152	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs543951781	chr7:66517189-66517190	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs561113936	chr7:66517192-66517193	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs529904501	chr7:66517216-66517217	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs546923877	chr7:66517220-66517221	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs566725977	chr7:66517227-66517228	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs370036469	chr7:66517342-66517343	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs551715360	chr7:66517363-66517364	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs528056301	chr7:66517423-66517424	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs541459668	chr7:66517424-66517425	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs185527802	chr7:66517533-66517534	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs151323838	chr7:66517625-66517626	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs374991806	chr7:66517650-66517651	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs561777795	chr7:66517653-66517654	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs567530968	chr7:66517700-66517701	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs369025762	chr7:66517730-66517731	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs10447523	chr7:66517741-66517742	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs553276399	chr7:66517742-66517743	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs190825693	chr7:66517745-66517746	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs545362409	chr7:66517766-66517767	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs558553043	chr7:66517767-66517768	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs202228413	chr7:66517771-66517772	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs544334368	chr7:66517807-66517808	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs56405861	chr7:66517811-66517812	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs533404308	chr7:66517812-66517813	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs540399914	chr7:66517821-66517822	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs180786494	chr7:66517829-66517830	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs567204308	chr7:66517840-66517841	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs185454157	chr7:66517859-66517860	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs571658953	chr7:66517879-66517880	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs530774008	chr7:66517893-66517894	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs138076029	chr7:66517918-66517919	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs149507545	chr7:66517919-66517920	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs536170084	chr7:66517930-66517931	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs370071608	chr7:66517941-66517942	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs7778191	chr7:66517950-66517951	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs566702915	chr7:66517983-66517984	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs188545817	chr7:66517989-66517990	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs11767549	chr7:66517991-66517992	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:91)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17170743	CNVD
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
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
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	22495311	CNVD
Follicular lymphoma	20505157	CNVD
Biliary cancer	19435499	CNVD
Williams-beuren syndrome	22470819	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Multiple myeloma	16461302	CNVD
Glioblastoma multiforme	21750150	CNVD
Cancer	21183584	CNVD
Hepatocellular carcinoma	16750200	CNVD
Non-small cell lung cancer	21829676	CNVD
Gastric cancer	24379144	CNVD
Glioblastoma multiforme	17002787	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Lissencephaly	21572526	CNVD
Breast cancer	17603634	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	16397240	CNVD
Acute myeloid leukemia	16864856	CNVD
Hodgkin''s lymphoma	18641027	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
Malignant fibrous histiocytomas	21085701	CNVD
Astrocytoma	22246337	CNVD
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
Acute monocytic leukemia	16498392	CNVD
Prostate cancer	16461572	CNVD
Salivary gland tumor	18059337	CNVD
Multiple myeloma	17550852	CNVD
Acute myeloid leukemia	21251322	CNVD
small cell lung cancer	20016488	CNVD
Bladder cancer	21909424	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Cancer	20164920	CNVD
Prostate cancer	18632612	CNVD
Myelofibrosis	22110671	CNVD
Lung cancer	21911935	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Neurodevelopmental disorder	22521361	CNVD
Burkitt''s lymphoma	20823134	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Lung cancer	20668451	CNVD
Prostate cancer	20601956	CNVD
Nasopharyngeal cancer	22815911	CNVD
Prostate cancer	21248069	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Prostate cancer	17297502	CNVD

Chromatin state (count:2374 , 50 per page) page: 1 2 3 4 5 6 7 ... 48

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:66483400-66551200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
2	chr7:66483600-66534400	Weak transcription	Aorta	Aorta
3	chr7:66486400-66531600	Weak transcription	Ovary	ovary
4	chr7:66487000-66576600	Weak transcription	Gastric	stomach
5	chr7:66495000-66532200	Weak transcription	HUES48 Cell Line	embryonic stem cell
6	chr7:66495200-66523000	Weak transcription	Esophagus	oesophagus
7	chr7:66495200-66523600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
8	chr7:66495200-66538000	Weak transcription	Brain Germinal Matrix	brain
9	chr7:66495200-66539400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
10	chr7:66495200-66597200	Weak transcription	Right Ventricle	heart
11	chr7:66495400-66529600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
12	chr7:66495400-66531800	Weak transcription	Fetal Kidney	kidney
13	chr7:66495400-66533200	Weak transcription	Thymus	Thymus
14	chr7:66495400-66534400	Weak transcription	Spleen	Spleen
15	chr7:66495600-66532200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
16	chr7:66495600-66533200	Weak transcription	HUES6 Cell Line	embryonic stem cell
17	chr7:66495600-66547400	Weak transcription	Pancreas	Pancrea
18	chr7:66498600-66534600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
19	chr7:66498600-66549400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
20	chr7:66500200-66525000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
21	chr7:66501000-66522600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
22	chr7:66501000-66540000	Weak transcription	Psoas Muscle	Psoas
23	chr7:66502400-66534400	Weak transcription	Lung	lung
24	chr7:66502400-66549600	Weak transcription	Brain Hippocampus Middle	brain
25	chr7:66506600-66534600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
26	chr7:66508000-66532200	Weak transcription	Fetal Muscle Trunk	muscle
27	chr7:66508000-66533400	Weak transcription	Colon Smooth Muscle	Colon
28	chr7:66508400-66522600	Weak transcription	Cortex derived primary cultured neurospheres	brain
29	chr7:66508800-66518400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
30	chr7:66508800-66520000	Weak transcription	Fetal Heart	heart
31	chr7:66508800-66528800	Weak transcription	Brain Anterior Caudate	brain
32	chr7:66508800-66533400	Weak transcription	Skeletal Muscle Male	skeletal muscle
33	chr7:66508800-66533800	Weak transcription	Hela-S3	cervix
34	chr7:66508800-66537600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
35	chr7:66508800-66538000	Weak transcription	A549	lung
36	chr7:66508800-66590400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
37	chr7:66509000-66523000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
38	chr7:66509000-66527400	Weak transcription	HSMMtube	muscle
39	chr7:66509000-66531200	Weak transcription	Muscle Satellite Cultured Cells	--
40	chr7:66509000-66531200	Weak transcription	Osteobl	bone
41	chr7:66509000-66533200	Weak transcription	HSMM	muscle
42	chr7:66509000-66538000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
43	chr7:66509000-66539600	Weak transcription	HMEC	breast
44	chr7:66509400-66533000	Weak transcription	Skeletal Muscle Female	skeletal muscle
45	chr7:66509400-66536600	Weak transcription	Rectal Smooth Muscle	rectum
46	chr7:66510800-66532000	Weak transcription	K562	blood
47	chr7:66511200-66537600	Weak transcription	Brain Substantia Nigra	brain
48	chr7:66511400-66539800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
49	chr7:66512000-66529200	Weak transcription	Primary B cells from cord blood	blood
50	chr7:66512000-66531600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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