Variant report

Variant	esv1829082
Chromosome Location	chr7:124503189-124556473
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:185)
CpG islands
(count:122)
Chromatin interactive
region (count:27)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:185 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr7:124547598-124547886	K562	blood:	n/a	n/a
2	ATF2	chr7:124533127-124533673	GM12878	blood:	n/a	n/a
3	ATF2	chr7:124533021-124534035	GM12878	blood:	n/a	n/a
4	BATF	chr7:124533246-124533843	GM12878	blood:	n/a	chr7:124533362-124533372
5	BATF	chr7:124533179-124533530	GM12878	blood:	n/a	chr7:124533362-124533372
6	BCL11A	chr7:124533121-124533611	GM12878	blood:	n/a	n/a
7	BCL3	chr7:124533131-124533577	GM12878	blood:	n/a	n/a
8	BCLAF1	chr7:124533247-124533646	GM12878	blood:	n/a	n/a
9	BHLHE40	chr7:124554502-124554557	GM12878	blood:	n/a	n/a
10	CEBPB	chr7:124522033-124522372	K562	blood:	n/a	chr7:124522229-124522240 chr7:124522094-124522107 chr7:124522094-124522107 chr7:124522227-124522240 chr7:124522229-124522238
11	CEBPB	chr7:124528270-124528553	HepG2	liver:	n/a	n/a
12	CEBPB	chr7:124516173-124516808	K562	blood:	n/a	n/a
13	CEBPB	chr7:124511829-124511919	K562	blood:	n/a	chr7:124511867-124511878
14	CEBPB	chr7:124528252-124528469	K562	blood:	n/a	n/a
15	CEBPB	chr7:124533035-124534036	GM12878	blood:	n/a	n/a
16	CEBPB	chr7:124511749-124512032	HepG2	liver:	n/a	chr7:124511867-124511878
17	CEBPB	chr7:124511758-124512013	A549	lung:	n/a	chr7:124511867-124511878
18	CEBPB	chr7:124522078-124522422	HepG2	liver:	n/a	chr7:124522229-124522240 chr7:124522094-124522107 chr7:124522094-124522107 chr7:124522227-124522240 chr7:124522229-124522238
19	CTCF	chr7:124509900-124510050	HCFaa	heart:	n/a	n/a
20	CTCF	chr7:124522239-124522436	K562	blood:	n/a	n/a
21	CTCF	chr7:124541294-124541326	Lung_OC	lung:	n/a	n/a
22	CTCF	chr7:124527201-124527225	GM13976	blood:	n/a	n/a
23	CTCF	chr7:124546245-124546280	GM13977	blood:	n/a	n/a
24	CUX1	chr7:124508461-124508529	GM12878	blood:	n/a	n/a
25	CUX1	chr7:124554439-124554621	GM12878	blood:	n/a	n/a
26	CUX1	chr7:124536969-124537169	K562	blood:	n/a	chr7:124537018-124537027
27	E2F4	chr7:124509320-124509547	MCF10A-Er-Src	breast:	n/a	n/a
28	E2F4	chr7:124519468-124519525	MCF10A-Er-Src	breast:	n/a	n/a
29	EP300	chr7:124533191-124533586	GM12878	blood:	n/a	chr7:124533307-124533321
30	EP300	chr7:124533214-124533732	GM12878	blood:	n/a	chr7:124533307-124533321
31	FOS	chr7:124525140-124525346	MCF10A-Er-Src	breast:	n/a	chr7:124525202-124525211 chr7:124525202-124525210 chr7:124525203-124525210 chr7:124525201-124525210
32	FOS	chr7:124548362-124548560	MCF10A-Er-Src	breast:	n/a	n/a
33	FOS	chr7:124525132-124525274	MCF10A-Er-Src	breast:	n/a	chr7:124525202-124525211 chr7:124525202-124525210 chr7:124525203-124525210 chr7:124525201-124525210
34	FOS	chr7:124548350-124548589	MCF10A-Er-Src	breast:	n/a	n/a
35	FOXM1	chr7:124533033-124533660	GM12878	blood:	n/a	n/a
36	FOXM1	chr7:124533063-124533864	GM12878	blood:	n/a	n/a
37	GATA3	chr7:124515603-124515739	SH-SY5Y	brain:	n/a	n/a
38	GATA3	chr7:124520878-124520879	SH-SY5Y	brain:	n/a	n/a
39	GATA3	chr7:124520028-124520099	SH-SY5Y	brain:	n/a	n/a
40	GATA3	chr7:124551485-124551734	SH-SY5Y	brain:	n/a	chr7:124551537-124551546
41	GATA3	chr7:124537483-124537550	SH-SY5Y	brain:	n/a	n/a
42	GATA3	chr7:124534688-124534797	SH-SY5Y	brain:	n/a	chr7:124534744-124534752
43	GATA3	chr7:124550459-124550499	SH-SY5Y	brain:	n/a	n/a
44	HCFC1	chr7:124527216-124527301	K562	blood:	n/a	n/a
45	IKZF1	chr7:124533189-124533820	GM12878	blood:	n/a	n/a
46	IRF1	chr7:124549045-124549062	K562	blood:	n/a	n/a
47	IRF1	chr7:124512284-124512517	K562	blood:	n/a	n/a
48	IRF1	chr7:124539465-124539758	K562	blood:	n/a	chr7:124539614-124539626 chr7:124539615-124539625
49	IRF1	chr7:124547685-124547796	K562	blood:	n/a	n/a
50	IRF1	chr7:124551630-124551634	K562	blood:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:124538660-124538710	SK-N-MC	brain:	n/a
2	chr7:124536676-124536726	GM19239	blood:	n/a
3	chr7:124536676-124536726	AG09309	skin:	n/a
4	chr7:124538660-124538710	HPAEpiC	pulmonary alveolar:	n/a
5	chr7:124538660-124538710	HCT-116	colon:	n/a
6	chr7:124538660-124538710	NHDF-neo	bronchial:	n/a
7	chr7:124536676-124536726	HCT-116	colon:	n/a
8	chr7:124536676-124536726	MCF10A-Er-Src	breast:	n/a
9	chr7:124536676-124536726	AG10803	skin:	n/a
10	chr7:124538660-124538710	AoSMC	blood vessel:	n/a
11	chr7:124538660-124538710	NT2-D1	testis:	n/a
12	chr7:124536676-124536726	ProgFib	skin:	n/a
13	chr7:124538660-124538710	GM12892	blood:	n/a
14	chr7:124538660-124538710	NHBE	bronchial:	n/a
15	chr7:124536676-124536726	GM06990	blood:	n/a
16	chr7:124538660-124538710	HEEpiC	esophagus:	n/a
17	chr7:124538660-124538710	PFSK-1	brain:	n/a
18	chr7:124536676-124536726	NH-A	brain:	n/a
19	chr7:124536676-124536726	MCF-7	breast:	n/a
20	chr7:124538660-124538710	LNCaP	prostate:	n/a
21	chr7:124536676-124536726	ECC-1	luminal epithelium:	n/a
22	chr7:124538660-124538710	PrEC	prostate:	n/a
23	chr7:124538660-124538710	AG09309	skin:	n/a
24	chr7:124538660-124538710	GM19239	blood:	n/a
25	chr7:124538660-124538710	NH-A	brain:	n/a
26	chr7:124538660-124538710	HRCEpiC	kidney:	n/a
27	chr7:124538660-124538710	ECC-1	luminal epithelium:	n/a
28	chr7:124538660-124538710	Hepatocyte	liver:	n/a
29	chr7:124536676-124536726	AG09319	gingival:	n/a
30	chr7:124536676-124536726	PrEC	prostate:	n/a
31	chr7:124536676-124536726	HNPCEpiC	eye:	n/a
32	chr7:124538660-124538710	K562	blood:	n/a
33	chr7:124538660-124538710	CMK	blood:	n/a
34	chr7:124538660-124538710	HCM	heart:	n/a
35	chr7:124536676-124536726	CMK	blood:	n/a
36	chr7:124538660-124538710	AG04449	skin:	fetal
37	chr7:124536676-124536726	SK-N-MC	brain:	n/a
38	chr7:124538660-124538710	HIPEpiC	eye:	n/a
39	chr7:124538660-124538710	HepG2	liver:	n/a
40	chr7:124536676-124536726	HPAEpiC	pulmonary alveolar:	n/a
41	chr7:124536676-124536726	HCF	heart:	n/a
42	chr7:124536676-124536726	PANC-1	pancreas:	n/a
43	chr7:124538660-124538710	HCPEpiC	choroid plexus:	n/a
44	chr7:124538660-124538710	IMR90	lung:	fetal
45	chr7:124538660-124538710	BJ	skin:	n/a
46	chr7:124538660-124538710	ProgFib	skin:	n/a
47	chr7:124538660-124538710	MCF-7	breast:	n/a
48	chr7:124538660-124538710	RPTEC	kidney:	n/a
49	chr7:124538660-124538710	HMEC	breast:	n/a
50	chr7:124536676-124536726	T-47D	breast:	n/a

(count:27 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:124522245..124524955-chr7:124533723..124536178,2	K562	blood:
2	chr7:124518995..124522486-chr7:124524978..124527724,3	K562	blood:
3	chr7:124520545..124522828-chr7:124555215..124557862,2	K562	blood:
4	chr7:124551396..124553692-chr7:124554817..124557525,2	K562	blood:
5	chr7:124523248..124524832-chr7:124524843..124527299,2	K562	blood:
6	chr7:124514345..124516702-chr7:124522638..124525470,2	K562	blood:
7	chr7:124501998..124504563-chr7:124508314..124510997,2	K562	blood:
8	chr7:124549176..124550827-chr7:124558825..124561252,2	K562	blood:
9	chr7:124522245..124524955-chr7:124533723..124536178,2	K562	blood:
10	chr7:124521370..124523136-chr7:124567552..124569550,2	K562	blood:
11	chr7:124523515..124526179-chr7:124527945..124529532,2	MCF-7	breast:
12	chr7:124524737..124527454-chr7:124559196..124561248,2	K562	blood:
13	chr7:124551396..124553692-chr7:124554817..124557525,2	K562	blood:
14	chr7:124509328..124512200-chr7:124525165..124526701,2	K562	blood:
15	chr7:124523515..124526179-chr7:124527945..124529532,2	MCF-7	breast:
16	chr7:124546480..124548936-chr7:124561383..124564382,2	K562	blood:
17	chr7:124504726..124507196-chr7:124509584..124511156,2	K562	blood:
18	chr7:124502317..124504649-chr7:124506280..124507789,2	K562	blood:
19	chr7:124520545..124522828-chr7:124555215..124557862,2	K562	blood:
20	chr7:124518995..124522486-chr7:124524978..124527724,3	K562	blood:
21	chr7:124534351..124537236-chr7:124567413..124569702,2	K562	blood:
22	chr7:124537777..124539651-chr7:124561497..124564089,2	K562	blood:
23	chr7:124514345..124516702-chr7:124522638..124525470,2	K562	blood:
24	chr7:124523248..124524832-chr7:124524843..124527299,2	K562	blood:
25	chr7:124504726..124507196-chr7:124509584..124511156,2	K562	blood:
26	chr7:124509328..124512200-chr7:124525165..124526701,2	K562	blood:
27	chr7:124550905..124554322-chr7:124566903..124570128,4	K562	blood:

(count:2 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GPR37-2	chr7:124555628-124555700	NONHSAT123087
2	lnc-GPR37-2	chr7:124538315-124538428	NONHSAT123087

No data

Variant related genes	Relation type
POT1	TF binding region
POT1	CpG island
ENSG00000128513	chromatin interactions
ENSG00000224897	chromatin interactions

Extended variants
information (count: 1798 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:1798 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs386717482	chr7:124503189-124503190	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs145784212	chr7:124503190-124503191	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs4397336	chr7:124503196-124503197	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
4	rs191888253	chr7:124503213-124503214	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs376846221	chr7:124503244-124503245	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs540780185	chr7:124503254-124503255	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs148536960	chr7:124503268-124503269	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs142749439	chr7:124503320-124503321	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs545995013	chr7:124503326-124503327	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs201236678	chr7:124503376-124503377	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs370277739	chr7:124503383-124503384	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs531577689	chr7:124503387-124503388	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs146150652	chr7:124503416-124503417	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs373691389	chr7:124503512-124503513	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs113602672	chr7:124503527-124503528	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs564097106	chr7:124503555-124503556	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs146552802	chr7:124503610-124503611	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs377547236	chr7:124503635-124503636	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs371168635	chr7:124503656-124503657	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs115093434	chr7:124503758-124503759	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs561639881	chr7:124503781-124503782	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs77854550	chr7:124503820-124503821	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs547524924	chr7:124503890-124503891	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs570578804	chr7:124503896-124503897	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs533011953	chr7:124503900-124503901	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs141390192	chr7:124503955-124503956	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs569812743	chr7:124503973-124503974	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs59045238	chr7:124503993-124503994	Weak transcription Strong transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs66526112	chr7:124504074-124504075	Weak transcription Strong transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs182268273	chr7:124504076-124504077	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs568723880	chr7:124504100-124504101	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs371738622	chr7:124504128-124504129	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs201187257	chr7:124504153-124504154	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs145179337	chr7:124504262-124504263	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs563786304	chr7:124504283-124504284	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs372140635	chr7:124504358-124504359	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs577349284	chr7:124504363-124504364	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs112000499	chr7:124504400-124504401	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs200771891	chr7:124504432-124504433	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs556236326	chr7:124504449-124504450	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs529490136	chr7:124504455-124504456	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs186478440	chr7:124504496-124504497	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs190467311	chr7:124504534-124504535	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs549136391	chr7:124504556-124504557	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs565850990	chr7:124504649-124504650	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs540984926	chr7:124504704-124504705	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs146006702	chr7:124504774-124504775	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs564432017	chr7:124504811-124504812	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs528600140	chr7:124504871-124504872	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs373264642	chr7:124504929-124504930	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:87)

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
Autism	22495311	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
Metanephric adenoma	20802469	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
Myelodysplastic syndrome	21251322	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
Biliary cancer	19435499	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Prostate cancer	23792589	CNVD
Adenocarcinoma	21044232	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Non-small cell lung cancer	19889201	CNVD
Acute myeloid leukemia	18000384	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Metastatic melanoma	18483359	CNVD
Autism	18414403	CNVD
Autism	19401682	CNVD
Autism	19546859	CNVD
Schizophrenia	19546859	CNVD
Tourette syndrome	19546859	CNVD
Melanoma	19188590	CNVD
Hepatocellular carcinoma	16785998	CNVD
Glioblastoma multiforme	18628472	CNVD
Basal cell lymphoma	21115979	CNVD
Breast cancer	21509527	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
small cell lung cancer	20016488	CNVD
Epilepsy	21635232	CNVD
Squamous cell cancer	20885788	CNVD
Myelofibrosis	22110671	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Myxofibrosarcoma	20639860	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:600 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:124461400-124530800	Weak transcription	NHDF-Ad	bronchial
2	chr7:124462200-124510200	Weak transcription	Brain Angular Gyrus	brain
3	chr7:124462200-124568200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
4	chr7:124462600-124504000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
5	chr7:124464000-124506400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
6	chr7:124464000-124510400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
7	chr7:124464200-124519400	Weak transcription	Brain Hippocampus Middle	brain
8	chr7:124464400-124508800	Weak transcription	Skeletal Muscle Male	skeletal muscle
9	chr7:124464600-124530600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
10	chr7:124466400-124540800	Weak transcription	Right Ventricle	heart
11	chr7:124466400-124562200	Weak transcription	Muscle Satellite Cultured Cells	--
12	chr7:124466600-124563400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
13	chr7:124466800-124540800	Weak transcription	Gastric	stomach
14	chr7:124467000-124508200	Weak transcription	Duodenum Mucosa	Duodenum
15	chr7:124467600-124530600	Weak transcription	NH-A	brain
16	chr7:124467800-124510600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
17	chr7:124474200-124509600	Weak transcription	HMEC	breast
18	chr7:124475400-124506000	Weak transcription	Fetal Kidney	kidney
19	chr7:124475400-124506000	Weak transcription	Fetal Lung	lung
20	chr7:124475400-124511400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
21	chr7:124477000-124530800	Weak transcription	Primary B cells from peripheral blood	blood
22	chr7:124482400-124508200	Weak transcription	Rectal Smooth Muscle	rectum
23	chr7:124482400-124508600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
24	chr7:124484200-124554400	Weak transcription	HUVEC	blood vessel
25	chr7:124486800-124504800	Weak transcription	HUES6 Cell Line	embryonic stem cell
26	chr7:124487000-124504200	Weak transcription	Brain Substantia Nigra	brain
27	chr7:124487200-124504400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
28	chr7:124487200-124534800	Weak transcription	Fetal Heart	heart
29	chr7:124488000-124506000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
30	chr7:124488000-124513200	Weak transcription	Primary T cells fromperipheralblood	blood
31	chr7:124488200-124506000	Weak transcription	HSMM	muscle
32	chr7:124488400-124531200	Weak transcription	Osteobl	bone
33	chr7:124488600-124506000	Weak transcription	K562	blood
34	chr7:124488600-124508200	Weak transcription	Rectal Mucosa Donor 29	rectum
35	chr7:124489200-124507600	Weak transcription	NHEK	skin
36	chr7:124489800-124503600	Weak transcription	Placenta	Placenta
37	chr7:124489800-124504600	Weak transcription	Esophagus	oesophagus
38	chr7:124490800-124540600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr7:124491400-124506200	Weak transcription	Fetal Muscle Leg	muscle
40	chr7:124491400-124506200	Weak transcription	Sigmoid Colon	Sigmoid Colon
41	chr7:124491600-124506000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
42	chr7:124491600-124508800	Weak transcription	HUES48 Cell Line	embryonic stem cell
43	chr7:124491800-124511200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
44	chr7:124492000-124506000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
45	chr7:124493000-124514400	Weak transcription	Duodenum Smooth Muscle	Duodenum
46	chr7:124498000-124506200	Weak transcription	Fetal Muscle Trunk	muscle
47	chr7:124498000-124529000	Weak transcription	Primary monocytes fromperipheralblood	blood
48	chr7:124498200-124503200	Weak transcription	Primary T helper cells fromperipheralblood	blood
49	chr7:124498200-124504600	Weak transcription	Pancreas	Pancrea
50	chr7:124498200-124504800	Weak transcription	Lung	lung

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