Variant report

Variant	esv15711
Chromosome Location	chr7:66739334-66760817
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:484)
CpG islands
(count:428)
Chromatin interactive
region (count:0)
LncRNA
region (count:14)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:484 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BATF	chr7:66740288-66740901	GM12878	blood:	n/a	n/a
2	BATF	chr7:66758680-66759069	GM12878	blood:	n/a	n/a
3	BATF	chr7:66740695-66740918	GM12878	blood:	n/a	n/a
4	BATF	chr7:66741002-66741170	GM12878	blood:	n/a	n/a
5	BCL11A	chr7:66758661-66759039	GM12878	blood:	n/a	n/a
6	BCL11A	chr7:66740294-66740829	GM12878	blood:	n/a	n/a
7	BCL11A	chr7:66742367-66742628	GM12878	blood:	n/a	n/a
8	BCL11A	chr7:66757474-66757666	GM12878	blood:	n/a	n/a
9	BCL11A	chr7:66749460-66749703	GM12878	blood:	n/a	n/a
10	BCL11A	chr7:66755476-66755763	GM12878	blood:	n/a	n/a
11	BCL11A	chr7:66741031-66741279	GM12878	blood:	n/a	n/a
12	BCL11A	chr7:66758736-66758964	GM12878	blood:	n/a	n/a
13	BCL11A	chr7:66740354-66740794	GM12878	blood:	n/a	n/a
14	BCL11A	chr7:66757441-66757675	GM12878	blood:	n/a	n/a
15	CEBPB	chr7:66745876-66746253	K562	blood:	n/a	n/a
16	CEBPB	chr7:66745889-66746082	A549	lung:	n/a	n/a
17	CEBPB	chr7:66746054-66746074	IMR90	lung:	n/a	n/a
18	CEBPB	chr7:66745879-66746079	HepG2	liver:	n/a	n/a
19	CTCF	chr7:66758833-66758900	LNCaP	prostate:	n/a	n/a
20	CTCF	chr7:66759582-66759609	LNCaP	prostate:	n/a	n/a
21	CTCF	chr7:66742040-66742190	GM12865	blood:	n/a	n/a
22	CTCF	chr7:66742140-66742290	HCT-116	colon:	n/a	n/a
23	CTCF	chr7:66760084-66760113	Medullo	brain:	n/a	n/a
24	CTCF	chr7:66744860-66745010	GM12866	blood:	n/a	n/a
25	CTCF	chr7:66742060-66742210	HCPEpiC	choroid plexus:	n/a	n/a
26	CTCF	chr7:66741962-66742228	A549	lung:	n/a	n/a
27	CTCF	chr7:66742015-66742215	K562	blood:	n/a	n/a
28	CTCF	chr7:66741891-66742338	A549	lung:	n/a	n/a
29	CTCF	chr7:66741959-66742363	K562	blood:	n/a	n/a
30	CTCF	chr7:66742120-66742270	GM06990	blood:	n/a	n/a
31	CTCF	chr7:66742123-66742206	H1-hESC	embryonic stem cell:	n/a	n/a
32	CTCF	chr7:66742060-66742210	HPF	lung:	n/a	n/a
33	CTCF	chr7:66742101-66742214	K562	blood:	n/a	n/a
34	CTCF	chr7:66742060-66742210	HPAF	blood vessel:	n/a	n/a
35	CTCF	chr7:66741947-66742345	A549	lung:	n/a	n/a
36	CTCF	chr7:66741963-66742247	K562	blood:	n/a	n/a
37	CTCF	chr7:66742120-66742270	HFF-Myc	foreskin:	n/a	n/a
38	CTCF	chr7:66742080-66742230	HVMF	connective:	n/a	n/a
39	CTCF	chr7:66742139-66742192	MCF-7	breast:	n/a	n/a
40	CTCF	chr7:66742116-66742207	Gliobla	brain:	n/a	n/a
41	CTCF	chr7:66742122-66742204	A549	lung:	n/a	n/a
42	CTCF	chr7:66742137-66742198	MCF-7	breast:	n/a	n/a
43	CTCF	chr7:66751098-66751163	GM10248	blood:	n/a	n/a
44	CTCF	chr7:66742120-66742270	WI-38	lung:	n/a	n/a
45	CTCF	chr7:66742119-66742231	Medullo	brain:	n/a	n/a
46	CTCF	chr7:66742019-66742208	IMR90	lung:	n/a	n/a
47	CTCF	chr7:66742080-66742230	HAc	cerebellar:	n/a	n/a
48	CTCF	chr7:66742135-66742221	LNCaP	prostate:	n/a	n/a
49	CTCF	chr7:66742136-66742195	GM12891	blood:	n/a	n/a
50	CTCF	chr7:66742016-66742202	GM12878	blood:	n/a	n/a

(count:428 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:66751227-66751277	HNPCEpiC	eye:	n/a
2	chr7:66751227-66751277	HNPCEpiC	eye:	n/a
3	chr7:66742988-66743038	HIPEpiC	eye:	n/a
4	chr7:66751257-66751307	NT2-D1	testis:	n/a
5	chr7:66751107-66751157	AoSMC	blood vessel:	n/a
6	chr7:66751257-66751307	HEK293	kidney:	embryo
7	chr7:66747538-66747588	NB4	blood:	n/a
8	chr7:66742988-66743038	MCF-7	breast:	n/a
9	chr7:66747538-66747588	Hela-S3	cervix:	n/a
10	chr7:66750978-66751028	IMR90	lung:	fetal
11	chr7:66751257-66751307	BJ	skin:	n/a
12	chr7:66742988-66743038	HEK293	kidney:	embryo
13	chr7:66747538-66747588	SKMC	muscle:	n/a
14	chr7:66751257-66751307	HCF	heart:	n/a
15	chr7:66751227-66751277	HEK293	kidney:	embryo
16	chr7:66751257-66751307	HCM	heart:	n/a
17	chr7:66751107-66751157	AG10803	skin:	n/a
18	chr7:66751107-66751157	GM12878	blood:	n/a
19	chr7:66750978-66751028	GM12878	blood:	n/a
20	chr7:66747538-66747588	ECC-1	luminal epithelium:	n/a
21	chr7:66751257-66751307	U87	brain:	n/a
22	chr7:66750978-66751028	HEEpiC	esophagus:	n/a
23	chr7:66751227-66751277	Hepatocyte	liver:	n/a
24	chr7:66747538-66747588	CMK	blood:	n/a
25	chr7:66751257-66751307	Jurkat	blood:	n/a
26	chr7:66751257-66751307	PANC-1	pancreas:	n/a
27	chr7:66751107-66751157	T-47D	breast:	n/a
28	chr7:66751257-66751307	HPAEpiC	pulmonary alveolar:	n/a
29	chr7:66750978-66751028	HAEpiC	amniotic membrane:	n/a
30	chr7:66742988-66743038	HL-60	blood:	n/a
31	chr7:66742988-66743038	Jurkat	blood:	n/a
32	chr7:66751107-66751157	A549	lung:	n/a
33	chr7:66749296-66749346	NT2-D1	testis:	n/a
34	chr7:66751257-66751307	SKMC	muscle:	n/a
35	chr7:66751227-66751277	HRCEpiC	kidney:	n/a
36	chr7:66742988-66743038	A549	lung:	n/a
37	chr7:66751107-66751157	GM12892	blood:	n/a
38	chr7:66751107-66751157	SK-N-SH	brain:	n/a
39	chr7:66751257-66751307	AG04449	skin:	fetal
40	chr7:66747538-66747588	GM12891	blood:	n/a
41	chr7:66751107-66751157	GM12891	blood:	n/a
42	chr7:66751107-66751157	HepG2	liver:	n/a
43	chr7:66751107-66751157	U87	brain:	n/a
44	chr7:66749296-66749346	K562	blood:	n/a
45	chr7:66750978-66751028	RPTEC	kidney:	n/a
46	chr7:66751257-66751307	HMEC	breast:	n/a
47	chr7:66742988-66743038	SK-N-MC	brain:	n/a
48	chr7:66750978-66751028	AG09309	skin:	n/a
49	chr7:66751227-66751277	HRPEpiC	eye:	n/a
50	chr7:66747538-66747588	BE2_C	brain:	n/a

No data

(count:14 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SBDS-17	chr7:66757447-66757536	NONHSAT121270
2	lnc-SBDS-17	chr7:66757450-66757536	NR_046299
3	lnc-SBDS-17	chr7:66760605-66760788	NONHSAT121270
4	lnc-SBDS-17	chr7:66741118-66741236	NR_046299
5	lnc-STAG3L4-5	chr7:66738714-66739487	NONHSAT121267
6	lnc-STAG3L4-5	chr7:66742324-66742413	NONHSAT121267
7	lnc-SBDS-17	chr7:66760605-66760788	NR_046299
8	lnc-STAG3L4-5	chr7:66738714-66739487	FPKM1_group_29835_transcript_4
9	lnc-SBDS-17	chr7:66757423-66757536	NR_022007
10	lnc-SBDS-17	chr7:66752527-66752706	NR_046297
11	lnc-SBDS-16	chr7:66742735-66743114	NONHSAT121268
12	lnc-SBDS-17	chr7:66757450-66757536	NR_046297
13	lnc-SBDS-17	chr7:66760605-66760788	NR_022007
14	lnc-SBDS-17	chr7:66760605-66760788	NR_046297

No data

Variant related genes	Relation type
ENSG00000230358	TF binding region
ENSG00000230358	CpG island

Extended variants
information (count: 684 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:684 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs58527194	chr7:66739441-66739442	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
2	rs547487400	chr7:66739467-66739468	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
3	rs7797286	chr7:66739524-66739525	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs58529342	chr7:66739527-66739528	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs191972972	chr7:66739548-66739549	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs139248206	chr7:66739558-66739559	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs184575133	chr7:66739573-66739574	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs189243155	chr7:66739577-66739578	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs58185188	chr7:66739703-66739704	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs193253389	chr7:66739769-66739770	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs562911172	chr7:66739770-66739771	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs112618679	chr7:66739805-66739806	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs201502496	chr7:66739819-66739820	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs71052419	chr7:66739838-66739839	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs60221285	chr7:66739841-66739842	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs368591053	chr7:66739858-66739859	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs191204832	chr7:66739872-66739873	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs185678321	chr7:66739873-66739874	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs554268403	chr7:66739984-66739985	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs577261730	chr7:66739996-66739997	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs546458280	chr7:66740012-66740013	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs369091632	chr7:66740017-66740018	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs563080872	chr7:66740089-66740090	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs3980794	chr7:66740153-66740154	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs199641960	chr7:66740232-66740233	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs9638239	chr7:66740398-66740399	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs9638240	chr7:66740672-66740673	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs9638241	chr7:66740705-66740706	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs368407564	chr7:66740728-66740729	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs370323629	chr7:66740786-66740787	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs527317886	chr7:66740788-66740789	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs547057751	chr7:66740807-66740808	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs375492904	chr7:66740904-66740905	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs202201540	chr7:66740905-66740906	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs374752090	chr7:66740929-66740930	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs542069457	chr7:66741006-66741007	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs532854901	chr7:66741007-66741008	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs549426047	chr7:66741016-66741017	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs569536862	chr7:66741048-66741049	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs201600678	chr7:66741087-66741088	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs372229684	chr7:66741090-66741091	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs535237888	chr7:66741095-66741096	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs555275864	chr7:66741121-66741122	Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
44	rs372480514	chr7:66741123-66741124	Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
45	rs565814265	chr7:66741124-66741125	Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
46	rs550238100	chr7:66741129-66741130	Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
47	rs58152480	chr7:66741130-66741131	Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
48	rs189310242	chr7:66741143-66741144	Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
49	rs375227765	chr7:66741187-66741188	Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
50	rs553869275	chr7:66741310-66741311	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:90)

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
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
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:71 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:66694800-66766600	Weak transcription	Brain Inferior Temporal Lobe	brain
2	chr7:66701600-66766600	Weak transcription	Skeletal Muscle Male	skeletal muscle
3	chr7:66717400-66766200	Weak transcription	Fetal Muscle Leg	muscle
4	chr7:66717400-66766400	Weak transcription	Stomach Smooth Muscle	stomach
5	chr7:66717600-66756200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
6	chr7:66717800-66766400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
7	chr7:66719000-66766400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
8	chr7:66719800-66766200	Weak transcription	Spleen	Spleen
9	chr7:66721800-66756000	Weak transcription	Fetal Intestine Small	intestine
10	chr7:66722400-66740600	Weak transcription	Primary T cells from cord blood	blood
11	chr7:66723800-66766400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr7:66725800-66766200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
13	chr7:66725800-66766400	Weak transcription	Adipose Nuclei	Adipose
14	chr7:66727600-66749600	Weak transcription	Aorta	Aorta
15	chr7:66727600-66766200	Weak transcription	Primary T helper cells fromperipheralblood	blood
16	chr7:66728600-66766600	Weak transcription	Brain Angular Gyrus	brain
17	chr7:66729000-66767000	Weak transcription	Gastric	stomach
18	chr7:66733200-66749800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
19	chr7:66733200-66766600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
20	chr7:66733400-66766800	Weak transcription	Lung	lung
21	chr7:66733800-66750200	Weak transcription	Fetal Stomach	stomach
22	chr7:66736400-66766600	Weak transcription	Brain Substantia Nigra	brain
23	chr7:66742200-66766400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
24	chr7:66742400-66766400	Weak transcription	Sigmoid Colon	Sigmoid Colon
25	chr7:66742600-66766800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
26	chr7:66747600-66766600	Weak transcription	Brain Hippocampus Middle	brain
27	chr7:66748200-66766800	Weak transcription	Ovary	ovary
28	chr7:66748400-66766400	Weak transcription	Brain Cingulate Gyrus	brain
29	chr7:66749000-66764800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
30	chr7:66749600-66766400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
31	chr7:66749600-66766400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
32	chr7:66749600-66766600	Weak transcription	Brain Anterior Caudate	brain
33	chr7:66749600-66766600	Weak transcription	Fetal Intestine Large	intestine
34	chr7:66749800-66750400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
35	chr7:66750200-66752600	Strong transcription	Fetal Stomach	stomach
36	chr7:66750200-66753000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
37	chr7:66750200-66753400	Weak transcription	HUES6 Cell Line	embryonic stem cell
38	chr7:66750200-66753800	Weak transcription	Liver	Liver
39	chr7:66750200-66756400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
40	chr7:66750400-66751000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chr7:66750400-66765600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
42	chr7:66750800-66754400	Weak transcription	Colonic Mucosa	Colon
43	chr7:66751000-66751200	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
44	chr7:66751000-66758800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
45	chr7:66751000-66766600	Weak transcription	Duodenum Smooth Muscle	Duodenum
46	chr7:66751000-66767000	Weak transcription	Placenta Amnion	Placenta Amnion
47	chr7:66751200-66756000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
48	chr7:66751200-66766400	Weak transcription	Primary T cells fromperipheralblood	blood
49	chr7:66751400-66752200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
50	chr7:66751800-66766200	Weak transcription	Skeletal Muscle Female	skeletal muscle

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