Variant report

Variant	nsv1012222
Chromosome Location	chr1:169903862-169950341
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	CEBPB	chr1:169915475-169915783	IMR90	lung:	n/a	chr1:169915539-169915552 chr1:169915541-169915550
2	CEBPB	chr1:169915356-169915820	Hela-S3	cervix:	n/a	chr1:169915539-169915552 chr1:169915541-169915550
3	CEBPB	chr1:169920115-169920364	K562	blood:	n/a	chr1:169920249-169920258 chr1:169920248-169920259 chr1:169920247-169920258
4	CEBPB	chr1:169920105-169920380	A549	lung:	n/a	chr1:169920249-169920258 chr1:169920248-169920259 chr1:169920247-169920258
5	CEBPB	chr1:169920135-169920408	HepG2	liver:	n/a	chr1:169920249-169920258 chr1:169920248-169920259 chr1:169920247-169920258
6	CEBPB	chr1:169915309-169915804	MCF-7	breast:	n/a	chr1:169915539-169915552 chr1:169915541-169915550
7	CEBPB	chr1:169915401-169915893	MCF-7	breast:	n/a	chr1:169915539-169915552 chr1:169915541-169915550
8	CEBPB	chr1:169920089-169920421	IMR90	lung:	n/a	chr1:169920249-169920258 chr1:169920248-169920259 chr1:169920247-169920258
9	CTCF	chr1:169914627-169914631	MCF-7	breast:	n/a	n/a
10	CTCF	chr1:169914555-169914672	MCF-7	breast:	n/a	n/a
11	CTCF	chr1:169914599-169914659	Fibrobl	skin:	n/a	n/a
12	CTCF	chr1:169932721-169932758	GM19240	blood:	n/a	n/a
13	CTCF	chr1:169914619-169914624	MCF-7	breast:	n/a	n/a
14	CTCF	chr1:169914572-169914617	MCF-7	breast:	n/a	n/a
15	CTCF	chr1:169926841-169926902	Kidney_OC	kidney:	n/a	n/a
16	CTCF	chr1:169944840-169944990	AG09319	gingival:	n/a	n/a
17	CUX1	chr1:169943514-169943612	K562	blood:	n/a	n/a
18	CUX1	chr1:169912649-169912714	GM12878	blood:	n/a	n/a
19	CUX1	chr1:169943282-169943471	GM12878	blood:	n/a	n/a
20	E2F4	chr1:169911118-169911167	MCF10A-Er-Src	breast:	n/a	n/a
21	ELK1	chr1:169913442-169913451	Hela-S3	cervix:	n/a	n/a
22	ELK4	chr1:169911490-169911926	Hela-S3	cervix:	n/a	chr1:169911879-169911890
23	EP300	chr1:169937349-169937727	SK-N-SH_RA	brain:	n/a	n/a
24	EP300	chr1:169911550-169911955	SK-N-SH_RA	brain:	n/a	chr1:169911649-169911659
25	EP300	chr1:169911556-169912032	SK-N-SH_RA	brain:	n/a	chr1:169911649-169911659
26	EP300	chr1:169903523-169903943	Hela-S3	cervix:	n/a	n/a
27	EP300	chr1:169922354-169922368	K562	blood:	n/a	n/a
28	EP300	chr1:169937342-169937642	SK-N-SH_RA	brain:	n/a	n/a
29	EP300	chr1:169937046-169937893	SK-N-SH	brain:	n/a	n/a
30	FOS	chr1:169911148-169911489	MCF10A-Er-Src	breast:	n/a	chr1:169911311-169911318 chr1:169911310-169911319 chr1:169911311-169911319
31	FOS	chr1:169903180-169903925	Hela-S3	cervix:	n/a	n/a
32	FOS	chr1:169911133-169911507	HUVEC	blood vessel:	n/a	chr1:169911311-169911318 chr1:169911310-169911319 chr1:169911311-169911319
33	FOS	chr1:169911088-169911415	MCF10A-Er-Src	breast:	n/a	chr1:169911311-169911318 chr1:169911310-169911319 chr1:169911311-169911319
34	FOS	chr1:169911133-169911465	MCF10A-Er-Src	breast:	n/a	chr1:169911311-169911318 chr1:169911310-169911319 chr1:169911311-169911319
35	FOS	chr1:169911131-169911433	MCF10A-Er-Src	breast:	n/a	chr1:169911311-169911318 chr1:169911310-169911319 chr1:169911311-169911319
36	FOS	chr1:169915443-169915573	MCF10A-Er-Src	breast:	n/a	n/a
37	FOXA1	chr1:169911491-169911950	T-47D	breast:	n/a	n/a
38	FOXA1	chr1:169911448-169911953	T-47D	breast:	n/a	n/a
39	FOXA2	chr1:169911102-169911547	A549	lung:	n/a	chr1:169911356-169911368
40	FOXM1	chr1:169911508-169912049	MCF-7	breast:	n/a	n/a
41	FOXM1	chr1:169903272-169904167	MCF-7	breast:	n/a	n/a
42	GATA2	chr1:169911407-169911814	HUVEC	blood vessel:	n/a	n/a
43	GATA2	chr1:169928101-169928458	SH-SY5Y	brain:	n/a	chr1:169928371-169928381 chr1:169928243-169928255
44	GATA2	chr1:169937314-169937695	SH-SY5Y	brain:	n/a	n/a
45	GATA3	chr1:169928128-169928498	SH-SY5Y	brain:	n/a	chr1:169928371-169928381 chr1:169928243-169928255
46	GATA3	chr1:169911405-169911989	T-47D	breast:	n/a	n/a
47	GATA3	chr1:169911410-169912015	MCF-7	breast:	n/a	n/a
48	GATA3	chr1:169915098-169916052	MCF-7	breast:	n/a	chr1:169916004-169916015 chr1:169915612-169915628
49	GATA3	chr1:169911278-169912069	SK-N-SH	brain:	n/a	n/a
50	GATA3	chr1:169915380-169915864	MCF-7	breast:	n/a	chr1:169915612-169915628

No.	Distal block	Cell Line	Cell type
1	chr1:169903817..169906654-chr1:169908531..169910584,2	K562	blood:
2	chr1:169909516..169911412-chr20:55839152..55841163,2	MCF-7	breast:
3	chr1:169858457..169860973-chr1:169907396..169909921,2	MCF-7	breast:
4	chr1:169904469..169905208-chr1:169979740..169980542,2	MCF-7	breast:
5	chr1:169883530..169886106-chr1:169901752..169904376,3	K562	blood:
6	chr1:169915601..169917304-chr1:169919424..169921809,3	MCF-7	breast:
7	chr1:169913226..169915577-chr1:169917390..169920061,2	MCF-7	breast:
8	chr1:169907968..169909649-chr1:169910615..169913475,2	K562	blood:
9	chr1:169861655..169864221-chr1:169940931..169943553,2	MCF-7	breast:
10	chr1:169913226..169915577-chr1:169917390..169920061,2	MCF-7	breast:
11	chr1:169909334..169912008-chr1:170041825..170044429,2	MCF-7	breast:
12	chr1:169863023..169865011-chr1:169913232..169916470,3	MCF-7	breast:
13	chr1:169860365..169863802-chr1:169902105..169905662,4	MCF-7	breast:
14	chr1:169906887..169908799-chr1:169914040..169915551,2	MCF-7	breast:
15	chr1:169898316..169900651-chr1:169903000..169904751,2	K562	blood:
16	chr1:169906887..169908799-chr1:169914040..169915551,2	MCF-7	breast:
17	chr1:169894940..169897093-chr1:169912669..169915603,2	MCF-7	breast:
18	chr1:169927495..169930307-chr1:170507858..170509808,2	K562	blood:
19	chr1:169942236..169943172-chrX:26753938..26754794,2	MCF-7	breast:
20	chr1:169915601..169917304-chr1:169919424..169921809,3	MCF-7	breast:
21	chr1:169903817..169906654-chr1:169908531..169910584,2	K562	blood:
22	chr1:169907968..169909649-chr1:169910615..169913475,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SCYL3-1	chr1:169927085-169927387	NONHSAT007483

Variant related genes	Relation type
RN7SL269P	TF binding region
ENSG00000120370	chromatin interactions
ENSG00000000457	chromatin interactions
ENSG00000101144	chromatin interactions
ENSG00000075945	chromatin interactions

Extended variants
information (count: 1590 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:1590 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs989054	chr1:169903862-169903863	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs529523998	chr1:169903888-169903889	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs374709116	chr1:169903890-169903891	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs553103305	chr1:169903892-169903893	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs191901184	chr1:169903921-169903922	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs551158686	chr1:169904012-169904013	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs569348072	chr1:169904013-169904014	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs539964438	chr1:169904045-169904046	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs551890639	chr1:169904196-169904197	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs566942138	chr1:169904278-169904279	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs115240859	chr1:169904333-169904334	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs546813481	chr1:169904337-169904338	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs555757072	chr1:169904352-169904353	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs574678418	chr1:169904372-169904373	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs568280864	chr1:169904390-169904391	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs535380214	chr1:169904405-169904406	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs535365447	chr1:169904508-169904509	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs478116	chr1:169904525-169904526	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
19	rs146730333	chr1:169904533-169904534	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs140358769	chr1:169904534-169904535	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs28372457	chr1:169904593-169904594	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs572570547	chr1:169904668-169904669	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs182883320	chr1:169904692-169904693	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs188949107	chr1:169904843-169904844	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs529639366	chr1:169904873-169904874	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs550983451	chr1:169904955-169904956	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs563132904	chr1:169904997-169904998	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs371210277	chr1:169905000-169905001	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs149898847	chr1:169905006-169905007	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs551970182	chr1:169905040-169905041	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs10919271	chr1:169905053-169905054	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs368593385	chr1:169905093-169905094	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs534238619	chr1:169905097-169905098	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs549443496	chr1:169905127-169905128	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs372293788	chr1:169905154-169905155	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs564765251	chr1:169905182-169905183	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs550874729	chr1:169905202-169905203	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs35671692	chr1:169905207-169905208	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs193240627	chr1:169905278-169905279	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs144972030	chr1:169905296-169905297	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs539265653	chr1:169905297-169905298	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs557492277	chr1:169905309-169905310	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs374796813	chr1:169905351-169905352	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs386368695	chr1:169905352-169905353	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs368105004	chr1:169905353-169905354	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs199882793	chr1:169905354-169905355	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs184466508	chr1:169905429-169905430	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs549350169	chr1:169905445-169905446	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs629593	chr1:169905449-169905450	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
50	rs569124245	chr1:169905453-169905454	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:95)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Autism	22495311	CNVD
Hepatocellular carcinoma	16750200	CNVD
Liposarcoma	21253554	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	21183584	CNVD
Multiple myeloma	16461302	CNVD
Rett syndrome	21593744	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Non-small cell lung cancer	21829676	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Neuroblastoma	21899760	CNVD
Bladder cancer	19088036	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Retinoblastoma	19183342	CNVD
Non-small cell lung cancer	21385341	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Chordoma	18071362	CNVD
Hepatocellular carcinoma	18803288	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Urothelial carcinoma	21177765	CNVD
Burkitt''s lymphoma	19759907	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Testicular germ cell tumor	18059402	CNVD
Trisomy 5 syndrome	21098271	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Breast cancer	21611746	CNVD
Neuroblastoma	18923191	CNVD
Soft tissue tumor	16732325	CNVD
Cancer	17060936	CNVD
Lung cancer	16740712	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Williams-beuren syndrome	16971481	CNVD
Developmental delay	21147756	CNVD
Burkitt''s lymphoma	20823134	CNVD
small cell lung cancer	20016488	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Lung cancer	18438408	CNVD
Cancer	20164920	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:402 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:169878400-169946200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
2	chr1:169884200-169913000	Weak transcription	Rectal Mucosa Donor 29	rectum
3	chr1:169885400-169913200	Weak transcription	Ovary	ovary
4	chr1:169886400-169913000	Weak transcription	Primary T cells fromperipheralblood	blood
5	chr1:169886600-169915600	Weak transcription	Stomach Smooth Muscle	stomach
6	chr1:169887000-169911400	Weak transcription	Left Ventricle	heart
7	chr1:169890800-169906200	Weak transcription	Primary T helper cells PMA-I stimulated	--
8	chr1:169891000-169911400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
9	chr1:169891000-169913200	Weak transcription	Adipose Nuclei	Adipose
10	chr1:169899200-169911400	Weak transcription	Sigmoid Colon	Sigmoid Colon
11	chr1:169901400-169913000	Weak transcription	Fetal Stomach	stomach
12	chr1:169901400-169913200	Weak transcription	Skeletal Muscle Male	skeletal muscle
13	chr1:169902600-169904000	Enhancers	Hela-S3	cervix
14	chr1:169902800-169904000	Enhancers	NHDF-Ad	bronchial
15	chr1:169903000-169904000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
16	chr1:169903000-169904000	Enhancers	Osteobl	bone
17	chr1:169903000-169904200	Enhancers	NH-A	brain
18	chr1:169903200-169904000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
19	chr1:169903200-169904000	Enhancers	Fetal Heart	heart
20	chr1:169903200-169904000	Enhancers	NHLF	lung
21	chr1:169903200-169904600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr1:169903200-169904600	Enhancers	Muscle Satellite Cultured Cells	--
23	chr1:169903200-169904600	Enhancers	Fetal Lung	lung
24	chr1:169903400-169904000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
25	chr1:169903400-169904200	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
26	chr1:169903400-169904200	Enhancers	A549	lung
27	chr1:169903400-169904200	Enhancers	HUVEC	blood vessel
28	chr1:169903400-169904800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
29	chr1:169903600-169904000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
30	chr1:169903600-169904000	Enhancers	Aorta	Aorta
31	chr1:169903600-169904000	Enhancers	HMEC	breast
32	chr1:169903600-169904200	Enhancers	NHEK	skin
33	chr1:169903800-169904000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
34	chr1:169903800-169909600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
35	chr1:169904000-169911200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
36	chr1:169904000-169911400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
37	chr1:169904000-169929800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
38	chr1:169904000-169934800	Weak transcription	Fetal Heart	heart
39	chr1:169904000-169949800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
40	chr1:169904000-170010400	Weak transcription	Aorta	Aorta
41	chr1:169904200-169911600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
42	chr1:169904600-169911000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
43	chr1:169905200-169915400	Weak transcription	GM12878-XiMat	blood
44	chr1:169907800-169913200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
45	chr1:169908200-169909600	Weak transcription	Esophagus	oesophagus
46	chr1:169909200-169946000	Weak transcription	Primary T cells from cord blood	blood
47	chr1:169909600-169909800	Enhancers	Esophagus	oesophagus
48	chr1:169909600-169910000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
49	chr1:169909600-169910000	Enhancers	Lung	lung
50	chr1:169909800-169913200	Weak transcription	Esophagus	oesophagus

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