Variant report

Variant	nsv1009843
Chromosome Location	chr1:169903077-169950341
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	chr1:169915401-169915893	MCF-7	breast:	n/a	chr1:169915539-169915552 chr1:169915541-169915550
2	CEBPB	chr1:169920115-169920364	K562	blood:	n/a	chr1:169920249-169920258 chr1:169920248-169920259 chr1:169920247-169920258
3	CEBPB	chr1:169915356-169915820	Hela-S3	cervix:	n/a	chr1:169915539-169915552 chr1:169915541-169915550
4	CEBPB	chr1:169920105-169920380	A549	lung:	n/a	chr1:169920249-169920258 chr1:169920248-169920259 chr1:169920247-169920258
5	CEBPB	chr1:169915475-169915783	IMR90	lung:	n/a	chr1:169915539-169915552 chr1:169915541-169915550
6	CEBPB	chr1:169920135-169920408	HepG2	liver:	n/a	chr1:169920249-169920258 chr1:169920248-169920259 chr1:169920247-169920258
7	CEBPB	chr1:169915309-169915804	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	chr1:169926841-169926902	Kidney_OC	kidney:	n/a	n/a
10	CTCF	chr1:169914555-169914672	MCF-7	breast:	n/a	n/a
11	CTCF	chr1:169914619-169914624	MCF-7	breast:	n/a	n/a
12	CTCF	chr1:169914627-169914631	MCF-7	breast:	n/a	n/a
13	CTCF	chr1:169914572-169914617	MCF-7	breast:	n/a	n/a
14	CTCF	chr1:169944840-169944990	AG09319	gingival:	n/a	n/a
15	CTCF	chr1:169932721-169932758	GM19240	blood:	n/a	n/a
16	CTCF	chr1:169914599-169914659	Fibrobl	skin:	n/a	n/a
17	CUX1	chr1:169943514-169943612	K562	blood:	n/a	n/a
18	CUX1	chr1:169943282-169943471	GM12878	blood:	n/a	n/a
19	CUX1	chr1:169912649-169912714	GM12878	blood:	n/a	n/a
20	E2F4	chr1:169911118-169911167	MCF10A-Er-Src	breast:	n/a	n/a
21	ELF1	chr1:169903412-169903843	MCF-7	breast:	n/a	n/a
22	ELK1	chr1:169913442-169913451	Hela-S3	cervix:	n/a	n/a
23	ELK4	chr1:169911490-169911926	Hela-S3	cervix:	n/a	chr1:169911879-169911890
24	EP300	chr1:169937046-169937893	SK-N-SH	brain:	n/a	n/a
25	EP300	chr1:169937349-169937727	SK-N-SH_RA	brain:	n/a	n/a
26	EP300	chr1:169903523-169903943	Hela-S3	cervix:	n/a	n/a
27	EP300	chr1:169911550-169911955	SK-N-SH_RA	brain:	n/a	chr1:169911649-169911659
28	EP300	chr1:169922354-169922368	K562	blood:	n/a	n/a
29	EP300	chr1:169937342-169937642	SK-N-SH_RA	brain:	n/a	n/a
30	EP300	chr1:169911556-169912032	SK-N-SH_RA	brain:	n/a	chr1:169911649-169911659
31	FOS	chr1:169911148-169911489	MCF10A-Er-Src	breast:	n/a	chr1:169911311-169911318 chr1:169911310-169911319 chr1:169911311-169911319
32	FOS	chr1:169911131-169911433	MCF10A-Er-Src	breast:	n/a	chr1:169911311-169911318 chr1:169911310-169911319 chr1:169911311-169911319
33	FOS	chr1:169915443-169915573	MCF10A-Er-Src	breast:	n/a	n/a
34	FOS	chr1:169903549-169903847	MCF10A-Er-Src	breast:	n/a	n/a
35	FOS	chr1:169911088-169911415	MCF10A-Er-Src	breast:	n/a	chr1:169911311-169911318 chr1:169911310-169911319 chr1:169911311-169911319
36	FOS	chr1:169911133-169911507	HUVEC	blood vessel:	n/a	chr1:169911311-169911318 chr1:169911310-169911319 chr1:169911311-169911319
37	FOS	chr1:169903180-169903925	Hela-S3	cervix:	n/a	n/a
38	FOS	chr1:169911133-169911465	MCF10A-Er-Src	breast:	n/a	chr1:169911311-169911318 chr1:169911310-169911319 chr1:169911311-169911319
39	FOXA1	chr1:169911491-169911950	T-47D	breast:	n/a	n/a
40	FOXA1	chr1:169911448-169911953	T-47D	breast:	n/a	n/a
41	FOXA2	chr1:169911102-169911547	A549	lung:	n/a	chr1:169911356-169911368
42	FOXM1	chr1:169911508-169912049	MCF-7	breast:	n/a	n/a
43	FOXM1	chr1:169903272-169904167	MCF-7	breast:	n/a	n/a
44	FOXP2	chr1:169903633-169903787	PFSK-1	brain:	n/a	n/a
45	GATA2	chr1:169911407-169911814	HUVEC	blood vessel:	n/a	n/a
46	GATA2	chr1:169928101-169928458	SH-SY5Y	brain:	n/a	chr1:169928371-169928381 chr1:169928243-169928255
47	GATA2	chr1:169937314-169937695	SH-SY5Y	brain:	n/a	n/a
48	GATA3	chr1:169936518-169936617	SH-SY5Y	brain:	n/a	n/a
49	GATA3	chr1:169903393-169904001	MCF-7	breast:	n/a	n/a
50	GATA3	chr1:169918241-169918770	SK-N-SH	brain:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:169898316..169900651-chr1:169903000..169904751,2	K562	blood:
2	chr1:169907968..169909649-chr1:169910615..169913475,2	K562	blood:
3	chr1:169915601..169917304-chr1:169919424..169921809,3	MCF-7	breast:
4	chr1:169894940..169897093-chr1:169912669..169915603,2	MCF-7	breast:
5	chr1:169860365..169863802-chr1:169902105..169905662,4	MCF-7	breast:
6	chr1:169863023..169865011-chr1:169913232..169916470,3	MCF-7	breast:
7	chr1:169903817..169906654-chr1:169908531..169910584,2	K562	blood:
8	chr1:169927495..169930307-chr1:170507858..170509808,2	K562	blood:
9	chr1:169909334..169912008-chr1:170041825..170044429,2	MCF-7	breast:
10	chr1:169909516..169911412-chr20:55839152..55841163,2	MCF-7	breast:
11	chr1:169913226..169915577-chr1:169917390..169920061,2	MCF-7	breast:
12	chr1:169858457..169860973-chr1:169907396..169909921,2	MCF-7	breast:
13	chr1:169904469..169905208-chr1:169979740..169980542,2	MCF-7	breast:
14	chr1:169942236..169943172-chrX:26753938..26754794,2	MCF-7	breast:
15	chr1:169907968..169909649-chr1:169910615..169913475,2	K562	blood:
16	chr1:169887846..169894353-chr1:169898169..169903456,7	K562	blood:
17	chr1:169913226..169915577-chr1:169917390..169920061,2	MCF-7	breast:
18	chr1:169883530..169886106-chr1:169901752..169904376,3	K562	blood:
19	chr1:169915601..169917304-chr1:169919424..169921809,3	MCF-7	breast:
20	chr1:169906887..169908799-chr1:169914040..169915551,2	MCF-7	breast:
21	chr1:169906887..169908799-chr1:169914040..169915551,2	MCF-7	breast:
22	chr1:169903817..169906654-chr1:169908531..169910584,2	K562	blood:
23	chr1:169861655..169864221-chr1:169940931..169943553,2	MCF-7	breast:

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

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

Extended variants
information (count: 1622 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:1622 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2750014	chr1:169903077-169903078	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs568741442	chr1:169903083-169903084	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs530482136	chr1:169903126-169903127	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs375540007	chr1:169903163-169903164	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs543112724	chr1:169903168-169903169	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs563414948	chr1:169903267-169903268	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs570107275	chr1:169903318-169903319	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs528798879	chr1:169903339-169903340	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs546872071	chr1:169903410-169903411	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs568346720	chr1:169903411-169903412	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs536070526	chr1:169903437-169903438	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs557241430	chr1:169903438-169903439	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs10919270	chr1:169903460-169903461	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
14	rs539502961	chr1:169903510-169903511	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs558229885	chr1:169903523-169903524	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs573267139	chr1:169903538-169903539	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs570677317	chr1:169903548-169903549	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs541373133	chr1:169903553-169903554	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs553324579	chr1:169903563-169903564	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs537812748	chr1:169903606-169903607	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs574608878	chr1:169903653-169903654	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs542016990	chr1:169903659-169903660	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs542589165	chr1:169903674-169903675	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs563289211	chr1:169903682-169903683	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs601355	chr1:169903688-169903689	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
26	rs545482365	chr1:169903696-169903697	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs113419390	chr1:169903714-169903715	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs528365276	chr1:169903756-169903757	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs563771045	chr1:169903801-169903802	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs528058020	chr1:169903809-169903810	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs546162390	chr1:169903827-169903828	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs72539617	chr1:169903861-169903862	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs989054	chr1:169903862-169903863	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs529523998	chr1:169903888-169903889	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs374709116	chr1:169903890-169903891	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs553103305	chr1:169903892-169903893	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs191901184	chr1:169903921-169903922	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs551158686	chr1:169904012-169904013	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs569348072	chr1:169904013-169904014	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs539964438	chr1:169904045-169904046	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs551890639	chr1:169904196-169904197	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs566942138	chr1:169904278-169904279	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs115240859	chr1:169904333-169904334	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs546813481	chr1:169904337-169904338	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs555757072	chr1:169904352-169904353	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs574678418	chr1:169904372-169904373	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs568280864	chr1:169904390-169904391	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs535380214	chr1:169904405-169904406	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs535365447	chr1:169904508-169904509	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs478116	chr1:169904525-169904526	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance

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:417 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:169876200-169903600	Weak transcription	Aorta	Aorta
2	chr1:169878400-169946200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
3	chr1:169884200-169913000	Weak transcription	Rectal Mucosa Donor 29	rectum
4	chr1:169885400-169913200	Weak transcription	Ovary	ovary
5	chr1:169885600-169903200	Weak transcription	Placenta Amnion	Placenta Amnion
6	chr1:169886400-169913000	Weak transcription	Primary T cells fromperipheralblood	blood
7	chr1:169886600-169915600	Weak transcription	Stomach Smooth Muscle	stomach
8	chr1:169887000-169911400	Weak transcription	Left Ventricle	heart
9	chr1:169890800-169906200	Weak transcription	Primary T helper cells PMA-I stimulated	--
10	chr1:169891000-169911400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
11	chr1:169891000-169913200	Weak transcription	Adipose Nuclei	Adipose
12	chr1:169894200-169903400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
13	chr1:169899200-169911400	Weak transcription	Sigmoid Colon	Sigmoid Colon
14	chr1:169901400-169903200	Weak transcription	Fetal Heart	heart
15	chr1:169901400-169903200	Weak transcription	Fetal Kidney	kidney
16	chr1:169901400-169903200	Weak transcription	Fetal Lung	lung
17	chr1:169901400-169903600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
18	chr1:169901400-169913000	Weak transcription	Fetal Stomach	stomach
19	chr1:169901400-169913200	Weak transcription	Skeletal Muscle Male	skeletal muscle
20	chr1:169901600-169903200	Weak transcription	Muscle Satellite Cultured Cells	--
21	chr1:169901800-169903200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr1:169901800-169903400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
23	chr1:169902600-169904000	Enhancers	Hela-S3	cervix
24	chr1:169902800-169903200	Weak transcription	NHLF	lung
25	chr1:169902800-169904000	Enhancers	NHDF-Ad	bronchial
26	chr1:169903000-169903800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
27	chr1:169903000-169904000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
28	chr1:169903000-169904000	Enhancers	Osteobl	bone
29	chr1:169903000-169904200	Enhancers	NH-A	brain
30	chr1:169903200-169903600	Enhancers	Fetal Kidney	kidney
31	chr1:169903200-169903800	Enhancers	Placenta Amnion	Placenta Amnion
32	chr1:169903200-169904000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
33	chr1:169903200-169904000	Enhancers	Fetal Heart	heart
34	chr1:169903200-169904000	Enhancers	NHLF	lung
35	chr1:169903200-169904600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
36	chr1:169903200-169904600	Enhancers	Muscle Satellite Cultured Cells	--
37	chr1:169903200-169904600	Enhancers	Fetal Lung	lung
38	chr1:169903400-169904000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
39	chr1:169903400-169904200	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
40	chr1:169903400-169904200	Enhancers	A549	lung
41	chr1:169903400-169904200	Enhancers	HUVEC	blood vessel
42	chr1:169903400-169904800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
43	chr1:169903600-169903800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
44	chr1:169903600-169904000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
45	chr1:169903600-169904000	Enhancers	Aorta	Aorta
46	chr1:169903600-169904000	Enhancers	HMEC	breast
47	chr1:169903600-169904200	Enhancers	NHEK	skin
48	chr1:169903800-169904000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
49	chr1:169903800-169909600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
50	chr1:169904000-169911200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin

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