Variant report

Variant	nsv967444
Chromosome Location	chr7:65992587-66013934
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:422)
CpG islands
(count:61)
Chromatin interactive
region (count:4)
LncRNA
region (count:12)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:422 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:66004801-66005242	K562	blood:	n/a	n/a
2	ARID3A	chr7:65995312-65995357	HepG2	liver:	n/a	n/a
3	ARID3A	chr7:66000495-66001263	HepG2	liver:	n/a	n/a
4	ATF1	chr7:66004897-66005229	K562	blood:	n/a	n/a
5	BACH1	chr7:66004928-66005056	K562	blood:	n/a	n/a
6	BHLHE40	chr7:66006360-66006478	K562	blood:	n/a	n/a
7	BHLHE40	chr7:66004895-66005261	K562	blood:	n/a	n/a
8	BHLHE40	chr7:66003163-66003197	K562	blood:	n/a	n/a
9	BRCA1	chr7:66000548-66000686	HepG2	liver:	n/a	n/a
10	BRCA1	chr7:66000946-66001224	HepG2	liver:	n/a	n/a
11	CBX3	chr7:66004750-66005669	K562	blood:	n/a	n/a
12	CBX3	chr7:66000871-66001223	K562	blood:	n/a	n/a
13	CBX3	chr7:66003856-66004305	K562	blood:	n/a	n/a
14	CCNT2	chr7:66004919-66005276	K562	blood:	n/a	n/a
15	CEBPB	chr7:65994948-65995114	HepG2	liver:	n/a	n/a
16	CEBPB	chr7:65998883-65998965	K562	blood:	n/a	chr7:65998942-65998953
17	CEBPB	chr7:65998840-65998991	HepG2	liver:	n/a	chr7:65998942-65998953
18	CEBPB	chr7:66007678-66007863	IMR90	lung:	n/a	n/a
19	CEBPB	chr7:65994018-65994110	HepG2	liver:	n/a	chr7:65994058-65994069
20	CEBPB	chr7:66000564-66000852	HepG2	liver:	n/a	chr7:66000719-66000730
21	CEBPB	chr7:65998873-65999042	Hela-S3	cervix:	n/a	chr7:65998942-65998953
22	CEBPB	chr7:66000416-66001110	HepG2	liver:	n/a	chr7:66000719-66000730
23	CEBPB	chr7:65998820-65999201	ECC-1	luminal epithelium:	n/a	chr7:65998942-65998953
24	CEBPB	chr7:66000520-66001150	HepG2	liver:	n/a	chr7:66000719-66000730
25	CEBPB	chr7:65998824-65999073	H1-hESC	embryonic stem cell:	n/a	chr7:65998942-65998953
26	CEBPB	chr7:66003664-66003730	K562	blood:	n/a	chr7:66003711-66003722
27	CEBPB	chr7:65998876-65999005	IMR90	lung:	n/a	chr7:65998942-65998953
28	CEBPB	chr7:66000583-66000835	K562	blood:	n/a	chr7:66000719-66000730
29	CEBPB	chr7:66000451-66000918	HepG2	liver:	n/a	chr7:66000719-66000730
30	CEBPB	chr7:65993618-65993699	HepG2	liver:	n/a	chr7:65993629-65993640
31	CEBPB	chr7:65994009-65994196	K562	blood:	n/a	chr7:65994058-65994069
32	CEBPB	chr7:65998887-65999039	A549	lung:	n/a	chr7:65998942-65998953
33	CEBPB	chr7:65993621-65993665	Hela-S3	cervix:	n/a	chr7:65993629-65993640
34	CEBPB	chr7:66001983-66001997	K562	blood:	n/a	n/a
35	CEBPB	chr7:66003652-66003852	HepG2	liver:	n/a	chr7:66003711-66003722
36	CEBPD	chr7:66004674-66005338	K562	blood:	n/a	n/a
37	CEBPD	chr7:66000603-66000800	HepG2	liver:	n/a	n/a
38	CEBPD	chr7:66004766-66005296	K562	blood:	n/a	n/a
39	CEBPD	chr7:66000542-66001249	HepG2	liver:	n/a	n/a
40	CHD2	chr7:66007693-66007829	Hela-S3	cervix:	n/a	n/a
41	CHD2	chr7:66006345-66006351	K562	blood:	n/a	n/a
42	CTCF	chr7:66012945-66012957	GM10248	blood:	n/a	n/a
43	CTCF	chr7:65999335-65999382	GM20000	blood:	n/a	n/a
44	CTCF	chr7:66001240-66001390	HepG2	liver:	n/a	n/a
45	CTCF	chr7:66000831-66000876	HepG2	liver:	n/a	n/a
46	CTCF	chr7:65994751-65994797	Kidney_OC	kidney:	n/a	n/a
47	CTCF	chr7:65999326-65999332	GM20000	blood:	n/a	n/a
48	CUX1	chr7:66004890-66005202	K562	blood:	n/a	n/a
49	EGR1	chr7:66003860-66004167	K562	blood:	n/a	n/a
50	ELF1	chr7:66001018-66001323	K562	blood:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:66001814-66001864	HEK293	kidney:	embryo
2	chr7:66001814-66001864	HRPEpiC	eye:	n/a
3	chr7:66001814-66001864	U87	brain:	n/a
4	chr7:66001814-66001864	HNPCEpiC	eye:	n/a
5	chr7:66001814-66001864	BE2_C	brain:	n/a
6	chr7:66001814-66001864	AG09319	gingival:	n/a
7	chr7:66001814-66001864	HRCEpiC	kidney:	n/a
8	chr7:66001814-66001864	GM12892	blood:	n/a
9	chr7:66001814-66001864	LNCaP	prostate:	n/a
10	chr7:66001814-66001864	HRE	kidney:	n/a
11	chr7:66001814-66001864	HUVEC	blood vessel:	n/a
12	chr7:66001814-66001864	NHDF-neo	bronchial:	n/a
13	chr7:66001814-66001864	SKMC	muscle:	n/a
14	chr7:66001814-66001864	SK-N-MC	brain:	n/a
15	chr7:66001814-66001864	HCF	heart:	n/a
16	chr7:66001814-66001864	HAEpiC	amniotic membrane:	n/a
17	chr7:66001814-66001864	MCF10A-Er-Src	breast:	n/a
18	chr7:66001814-66001864	SK-N-SH_RA	brain:	n/a
19	chr7:66001814-66001864	Jurkat	blood:	n/a
20	chr7:66001814-66001864	T-47D	breast:	n/a
21	chr7:66001814-66001864	HCT-116	colon:	n/a
22	chr7:66001814-66001864	HL-60	blood:	n/a
23	chr7:66001814-66001864	ProgFib	skin:	n/a
24	chr7:66001814-66001864	Hela-S3	cervix:	n/a
25	chr7:66001814-66001864	SK-N-SH	brain:	n/a
26	chr7:66001814-66001864	ovcar-3	ovarian:	n/a
27	chr7:66001814-66001864	AG09309	skin:	n/a
28	chr7:66001814-66001864	SAEC	small airway:	n/a
29	chr7:66001814-66001864	GM12891	blood:	n/a
30	chr7:66001814-66001864	HCPEpiC	choroid plexus:	n/a
31	chr7:66001814-66001864	BJ	skin:	n/a
32	chr7:66001814-66001864	AG04449	skin:	fetal
33	chr7:66001814-66001864	AG10803	skin:	n/a
34	chr7:66001814-66001864	GM12878	blood:	n/a
35	chr7:66001814-66001864	NB4	blood:	n/a
36	chr7:66001814-66001864	Caco-2	colon:	n/a
37	chr7:66001814-66001864	Hepatocyte	liver:	n/a
38	chr7:66001814-66001864	AG04450	lung:	fetal
39	chr7:66001814-66001864	PrEC	prostate:	n/a
40	chr7:66001814-66001864	HIPEpiC	eye:	n/a
41	chr7:66001814-66001864	PANC-1	pancreas:	n/a
42	chr7:66001814-66001864	GM06990	blood:	n/a
43	chr7:66001814-66001864	HEEpiC	esophagus:	n/a
44	chr7:66001814-66001864	NH-A	brain:	n/a
45	chr7:66001814-66001864	HMEC	breast:	n/a
46	chr7:66001814-66001864	CMK	blood:	n/a
47	chr7:66001814-66001864	PFSK-1	brain:	n/a
48	chr7:66001814-66001864	GM19239	blood:	n/a
49	chr7:66001814-66001864	HCM	heart:	n/a
50	chr7:66001814-66001864	NT2-D1	testis:	n/a

(count:4 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:66013223..66015993-chr7:66016033..66017607,2	K562	blood:
2	chr7:66000362..66002580-chr7:66007526..66009182,2	MCF-7	breast:
3	chr7:65996716..65999287-chr7:66000647..66003151,2	K562	blood:
4	chr7:65996716..65999287-chr7:66000647..66003151,2	K562	blood:

(count:12 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-VKORC1L1-2	chr7:66006231-66007536	ENSG00000249705
2	lnc-SBDS-4	chr7:66006229-66007536	NONHSAT121200
3	lnc-SBDS-4	chr7:65994516-65995124	NONHSAT121202
4	lnc-SBDS-4	chr7:65996778-65996819	NONHSAT121202
5	lnc-SBDS-4	chr7:65991075-65996858	ENSG00000229180.4
6	lnc-SBDS-4	chr7:66006229-66006924	NONHSAT121204
7	lnc-SBDS-4	chr7:66004846-66004872	NONHSAT121204
8	lnc-VKORC1L1-2	chr7:65993448-65996860	ENSG00000249705
9	lnc-SBDS-4	chr7:66006229-66007536	ENSG00000229180.4
10	lnc-SBDS-4	chr7:65992918-65996858	NONHSAT121200
11	lnc-SBDS-4	chr7:65993425-65996858	ENSG00000229180
12	lnc-SBDS-4	chr7:66006229-66007536	ENSG00000229180

No data

Variant related genes	Relation type
ENSG00000229180	TF binding region
ENSG00000229180	CpG island
ENSG00000229180	chromatin interactions
SHCBP1	miRNA target sites
KCNK1	miRNA target sites

Extended variants
information (count: 963 )
Associated
traits (count: 80 )

Variant overlapped rSNPs/rCNVs (count:963 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs567007475	chr7:65992604-65992605	Weak transcription Strong transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
2	rs190734924	chr7:65992699-65992700	Weak transcription Strong transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
3	rs540245757	chr7:65992703-65992704	Weak transcription Strong transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
4	rs559042501	chr7:65992730-65992731	Weak transcription Strong transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
5	rs560497931	chr7:65992777-65992778	Weak transcription Strong transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
6	rs182963745	chr7:65992784-65992785	Weak transcription Strong transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
7	rs537810185	chr7:65992806-65992807	Weak transcription Strong transcription Enhancers Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
8	rs370264828	chr7:65992810-65992811	Weak transcription Strong transcription Enhancers Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
9	rs188107094	chr7:65992811-65992812	Weak transcription Strong transcription Enhancers Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
10	rs3735150	chr7:65992848-65992849	Weak transcription Strong transcription Enhancers Genic enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
11	rs536075270	chr7:65992876-65992877	Weak transcription Strong transcription Enhancers Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
12	rs3832486	chr7:65992905-65992906	Weak transcription Strong transcription Enhancers Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
13	rs397840738	chr7:65992913-65992914	Weak transcription Strong transcription Enhancers Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
14	rs191376531	chr7:65993004-65993005	Weak transcription Strong transcription Enhancers Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
15	rs543185941	chr7:65993016-65993017	Weak transcription Strong transcription Enhancers Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
16	rs572648580	chr7:65993025-65993026	Weak transcription Strong transcription Enhancers Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
17	rs1819974	chr7:65993115-65993116	Weak transcription Strong transcription Enhancers Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
18	rs182749792	chr7:65993125-65993126	Weak transcription Strong transcription Enhancers Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
19	rs564784922	chr7:65993217-65993218	Weak transcription Strong transcription Enhancers Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
20	rs187871238	chr7:65993219-65993220	Weak transcription Strong transcription Enhancers Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
21	rs371521537	chr7:65993259-65993260	Weak transcription Strong transcription Enhancers Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
22	rs191121257	chr7:65993317-65993318	Weak transcription Strong transcription Enhancers Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
23	rs561827162	chr7:65993318-65993319	Weak transcription Strong transcription Enhancers Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
24	rs116469066	chr7:65993328-65993329	Weak transcription Strong transcription Enhancers Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
25	rs4718361	chr7:65993444-65993445	Weak transcription Strong transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
26	rs547257118	chr7:65993449-65993450	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
27	rs560668151	chr7:65993450-65993451	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
28	rs532708803	chr7:65993461-65993462	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
29	rs551109468	chr7:65993508-65993509	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
30	rs569219166	chr7:65993512-65993513	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
31	rs538262092	chr7:65993537-65993538	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
32	rs548268590	chr7:65993543-65993544	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
33	rs183327720	chr7:65993546-65993547	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
34	rs536136287	chr7:65993565-65993566	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
35	rs552801639	chr7:65993601-65993602	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
36	rs572707407	chr7:65993624-65993625	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
37	rs538408599	chr7:65993625-65993626	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
38	rs569256752	chr7:65993640-65993641	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
39	rs575225901	chr7:65993656-65993657	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
40	rs544232096	chr7:65993661-65993662	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
41	rs201618000	chr7:65993674-65993675	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
42	rs73373337	chr7:65993675-65993676	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
43	rs575260432	chr7:65993683-65993684	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
44	rs540933004	chr7:65993704-65993705	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
45	rs560727449	chr7:65993734-65993735	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
46	rs13224048	chr7:65993766-65993767	Weak transcription Strong transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
47	rs13224057	chr7:65993792-65993793	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
48	rs552468145	chr7:65993833-65993834	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
49	rs563029728	chr7:65993853-65993854	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
50	rs531701975	chr7:65993900-65993901	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a

Variant related diseases (count:80)

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
Glioblastoma	21080181	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
Breast cancer	21990379	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	21399695	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
Non-syndromic sensorineural hearing loss	17122850	CNVD
Cancer	20164920	CNVD
Pancreatic cancer	17952125	CNVD
Prostate cancer	18632612	CNVD

Chromatin state (count:716 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:65981400-66001000	Weak transcription	Fetal Brain Female	brain
2	chr7:65983400-66001800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
3	chr7:65983400-66006000	Weak transcription	Placenta Amnion	Placenta Amnion
4	chr7:65983600-65994400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
5	chr7:65983600-66000400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
6	chr7:65985600-65994600	Weak transcription	Spleen	Spleen
7	chr7:65985800-66006200	Weak transcription	Pancreas	Pancrea
8	chr7:65986200-65993200	Weak transcription	Adipose Nuclei	Adipose
9	chr7:65986400-65994600	Weak transcription	HepG2	liver
10	chr7:65987400-65994800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
11	chr7:65987600-65994400	Weak transcription	Right Ventricle	heart
12	chr7:65987800-65995000	Weak transcription	Brain Hippocampus Middle	brain
13	chr7:65987800-66006200	Weak transcription	Gastric	stomach
14	chr7:65988000-65992800	Weak transcription	Liver	Liver
15	chr7:65988000-65993800	Weak transcription	Ovary	ovary
16	chr7:65988000-65995000	Weak transcription	Brain Angular Gyrus	brain
17	chr7:65988200-65992600	Weak transcription	Fetal Muscle Trunk	muscle
18	chr7:65988200-65994400	Weak transcription	Brain Anterior Caudate	brain
19	chr7:65988400-65993800	Weak transcription	Primary T cells from cord blood	blood
20	chr7:65988400-65994400	Weak transcription	Duodenum Smooth Muscle	Duodenum
21	chr7:65988400-66006200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
22	chr7:65988600-66006200	Weak transcription	Primary neutrophils fromperipheralblood	blood
23	chr7:65988600-66009000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
24	chr7:65988600-66009000	Weak transcription	HSMMtube	muscle
25	chr7:65988800-65994600	Weak transcription	NHLF	lung
26	chr7:65988800-65996000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
27	chr7:65988800-66008200	Weak transcription	Primary T cells fromperipheralblood	blood
28	chr7:65989000-66006200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
29	chr7:65989000-66007600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
30	chr7:65989400-65996800	Strong transcription	Fetal Stomach	stomach
31	chr7:65989400-65998800	Weak transcription	Right Atrium	heart
32	chr7:65989600-65996400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
33	chr7:65989600-65997000	Strong transcription	Fetal Intestine Small	intestine
34	chr7:65989800-65993800	Weak transcription	Fetal Intestine Large	intestine
35	chr7:65989800-65994400	Weak transcription	Aorta	Aorta
36	chr7:65989800-65994800	Weak transcription	Rectal Mucosa Donor 29	rectum
37	chr7:65989800-65995000	Weak transcription	Placenta	Placenta
38	chr7:65989800-66004200	Weak transcription	Dnd41	blood
39	chr7:65990000-65993000	Weak transcription	Fetal Muscle Leg	muscle
40	chr7:65990000-66009000	Weak transcription	Rectal Smooth Muscle	rectum
41	chr7:65990200-65993000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
42	chr7:65990400-65992600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
43	chr7:65990600-65994400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
44	chr7:65990600-65994400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
45	chr7:65990600-66004000	Weak transcription	HUES6 Cell Line	embryonic stem cell
46	chr7:65990600-66005600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
47	chr7:65990800-65992800	Weak transcription	Stomach Smooth Muscle	stomach
48	chr7:65991000-65992800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
49	chr7:65991000-65993000	Weak transcription	Lung	lung
50	chr7:65991200-66009800	Weak transcription	Small Intestine	intestine

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