Variant report

Variant	nsv1007190
Chromosome Location	chr1:169890542-169929582
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	ARID3A	chr1:169898074-169898510	K562	blood:	n/a	n/a
2	ARID3A	chr1:169898085-169898379	HepG2	liver:	n/a	n/a
3	BCLAF1	chr1:169897998-169898407	GM12878	blood:	n/a	n/a
4	BHLHE40	chr1:169895312-169895694	GM12878	blood:	n/a	n/a
5	CBX3	chr1:169897990-169898402	HCT-116	colon:	n/a	n/a
6	CEBPB	chr1:169920115-169920364	K562	blood:	n/a	chr1:169920249-169920258 chr1:169920248-169920259 chr1:169920247-169920258
7	CEBPB	chr1:169897984-169898391	HCT-116	colon:	n/a	n/a
8	CEBPB	chr1:169915401-169915893	MCF-7	breast:	n/a	chr1:169915539-169915552 chr1:169915541-169915550
9	CEBPB	chr1:169915475-169915783	IMR90	lung:	n/a	chr1:169915539-169915552 chr1:169915541-169915550
10	CEBPB	chr1:169920105-169920380	A549	lung:	n/a	chr1:169920249-169920258 chr1:169920248-169920259 chr1:169920247-169920258
11	CEBPB	chr1:169920135-169920408	HepG2	liver:	n/a	chr1:169920249-169920258 chr1:169920248-169920259 chr1:169920247-169920258
12	CEBPB	chr1:169920089-169920421	IMR90	lung:	n/a	chr1:169920249-169920258 chr1:169920248-169920259 chr1:169920247-169920258
13	CEBPB	chr1:169915356-169915820	Hela-S3	cervix:	n/a	chr1:169915539-169915552 chr1:169915541-169915550
14	CEBPB	chr1:169895158-169895662	MCF-7	breast:	n/a	n/a
15	CEBPB	chr1:169915309-169915804	MCF-7	breast:	n/a	chr1:169915539-169915552 chr1:169915541-169915550
16	CHD1	chr1:169898365-169898449	GM12878	blood:	n/a	n/a
17	CTCF	chr1:169898100-169898250	HAc	cerebellar:	n/a	chr1:169898236-169898244 chr1:169898231-169898249
18	CTCF	chr1:169898180-169898330	HCPEpiC	choroid plexus:	n/a	chr1:169898233-169898254 chr1:169898236-169898244 chr1:169898231-169898249
19	CTCF	chr1:169898220-169898370	GM12872	blood:	n/a	chr1:169898233-169898254 chr1:169898236-169898244 chr1:169898231-169898249
20	CTCF	chr1:169914572-169914617	MCF-7	breast:	n/a	n/a
21	CTCF	chr1:169898120-169898270	GM12872	blood:	n/a	chr1:169898233-169898254 chr1:169898236-169898244 chr1:169898231-169898249
22	CTCF	chr1:169898180-169898330	HEEpiC	esophagus:	n/a	chr1:169898233-169898254 chr1:169898236-169898244 chr1:169898231-169898249
23	CTCF	chr1:169898260-169898410	WI-38	lung:	n/a	n/a
24	CTCF	chr1:169898140-169898290	RPTEC	kidney:	n/a	chr1:169898233-169898254 chr1:169898236-169898244 chr1:169898231-169898249
25	CTCF	chr1:169898121-169898332	Kidney_OC	kidney:	n/a	chr1:169898233-169898254 chr1:169898236-169898244 chr1:169898231-169898249
26	CTCF	chr1:169898140-169898290	GM12801	blood:	n/a	chr1:169898233-169898254 chr1:169898236-169898244 chr1:169898231-169898249
27	CTCF	chr1:169898140-169898290	NHDF-neo	bronchial:	n/a	chr1:169898233-169898254 chr1:169898236-169898244 chr1:169898231-169898249
28	CTCF	chr1:169898120-169898270	GM12873	blood:	n/a	chr1:169898233-169898254 chr1:169898236-169898244 chr1:169898231-169898249
29	CTCF	chr1:169898200-169898350	HPF	lung:	n/a	chr1:169898233-169898254 chr1:169898236-169898244 chr1:169898231-169898249
30	CTCF	chr1:169898160-169898310	HEEpiC	esophagus:	n/a	chr1:169898233-169898254 chr1:169898236-169898244 chr1:169898231-169898249
31	CTCF	chr1:169898160-169898310	WERI-Rb-1	eye:	n/a	chr1:169898233-169898254 chr1:169898236-169898244 chr1:169898231-169898249
32	CTCF	chr1:169898060-169898421	A549	lung:	n/a	chr1:169898233-169898254 chr1:169898236-169898244 chr1:169898231-169898249
33	CTCF	chr1:169898079-169898332	SK-N-SH_RA	brain:	n/a	chr1:169898233-169898254 chr1:169898236-169898244 chr1:169898231-169898249
34	CTCF	chr1:169914599-169914659	Fibrobl	skin:	n/a	n/a
35	CTCF	chr1:169898180-169898330	HUVEC	blood vessel:	n/a	chr1:169898233-169898254 chr1:169898236-169898244 chr1:169898231-169898249
36	CTCF	chr1:169898160-169898310	NHDF-neo	bronchial:	n/a	chr1:169898233-169898254 chr1:169898236-169898244 chr1:169898231-169898249
37	CTCF	chr1:169898160-169898310	GM12874	blood:	n/a	chr1:169898233-169898254 chr1:169898236-169898244 chr1:169898231-169898249
38	CTCF	chr1:169898300-169898450	A549	lung:	n/a	n/a
39	CTCF	chr1:169897860-169898010	AoAF	blood vessel:	n/a	n/a
40	CTCF	chr1:169898180-169898330	GM12869	blood:	n/a	chr1:169898233-169898254 chr1:169898236-169898244 chr1:169898231-169898249
41	CTCF	chr1:169898140-169898290	SAEC	small airway:	n/a	chr1:169898233-169898254 chr1:169898236-169898244 chr1:169898231-169898249
42	CTCF	chr1:169898100-169898250	GM12866	blood:	n/a	chr1:169898236-169898244 chr1:169898231-169898249
43	CTCF	chr1:169898140-169898290	AoAF	blood vessel:	n/a	chr1:169898233-169898254 chr1:169898236-169898244 chr1:169898231-169898249
44	CTCF	chr1:169898139-169898327	LNCaP	prostate:	n/a	chr1:169898233-169898254 chr1:169898236-169898244 chr1:169898231-169898249
45	CTCF	chr1:169898080-169898230	HVMF	connective:	n/a	n/a
46	CTCF	chr1:169898080-169898230	HAc	cerebellar:	n/a	n/a
47	CTCF	chr1:169898200-169898350	GM12870	blood:	n/a	chr1:169898233-169898254 chr1:169898236-169898244 chr1:169898231-169898249
48	CTCF	chr1:169914619-169914624	MCF-7	breast:	n/a	n/a
49	CTCF	chr1:169898160-169898310	AG09309	skin:	n/a	chr1:169898233-169898254 chr1:169898236-169898244 chr1:169898231-169898249
50	CTCF	chr1:169898140-169898290	HL-60	blood:	n/a	chr1:169898233-169898254 chr1:169898236-169898244 chr1:169898231-169898249

No.	Distal block	Cell Line	Cell type
1	chr1:169915601..169917304-chr1:169919424..169921809,3	MCF-7	breast:
2	chr1:169898316..169900651-chr1:169903000..169904751,2	K562	blood:
3	chr1:169858457..169860973-chr1:169907396..169909921,2	MCF-7	breast:
4	chr1:169887846..169894353-chr1:169898169..169903456,7	K562	blood:
5	chr1:169863260..169865221-chr1:169889034..169890676,2	MCF-7	breast:
6	chr1:169903817..169906654-chr1:169908531..169910584,2	K562	blood:
7	chr1:169891530..169894353-chr1:169899147..169901987,3	K562	blood:
8	chr1:169894940..169897093-chr1:169912669..169915603,2	MCF-7	breast:
9	chr1:169906887..169908799-chr1:169914040..169915551,2	MCF-7	breast:
10	chr1:169907968..169909649-chr1:169910615..169913475,2	K562	blood:
11	chr1:169862018..169863594-chr1:169891120..169892804,2	MCF-7	breast:
12	chr1:169894940..169897093-chr1:169912669..169915603,2	MCF-7	breast:
13	chr1:169927495..169930307-chr1:170507858..170509808,2	K562	blood:
14	chr1:169897753..169898707-chr1:170850760..170851657,6	MCF-7	breast:
15	chr1:169904469..169905208-chr1:169979740..169980542,2	MCF-7	breast:
16	chr1:169897891..169898773-chr1:170898615..170899541,2	MCF-7	breast:
17	chr1:169903817..169906654-chr1:169908531..169910584,2	K562	blood:
18	chr1:169909516..169911412-chr20:55839152..55841163,2	MCF-7	breast:
19	chr1:169897805..169898496-chr1:170898617..170899529,4	MCF-7	breast:
20	chr1:169819515..169822344-chr1:169896401..169898488,2	MCF-7	breast:
21	chr1:169863023..169865011-chr1:169913232..169916470,3	MCF-7	breast:
22	chr1:169915601..169917304-chr1:169919424..169921809,3	MCF-7	breast:
23	chr1:169887846..169894353-chr1:169898169..169903456,7	K562	blood:
24	chr1:169913226..169915577-chr1:169917390..169920061,2	MCF-7	breast:
25	chr1:169883530..169886106-chr1:169901752..169904376,3	K562	blood:
26	chr1:169897755..169898590-chr1:170734743..170735498,2	MCF-7	breast:
27	chr1:169906887..169908799-chr1:169914040..169915551,2	MCF-7	breast:
28	chr1:169860365..169863802-chr1:169902105..169905662,4	MCF-7	breast:
29	chr1:169909334..169912008-chr1:170041825..170044429,2	MCF-7	breast:
30	chr1:169913226..169915577-chr1:169917390..169920061,2	MCF-7	breast:
31	chr1:169862245..169864105-chr1:169894595..169896381,2	MCF-7	breast:
32	chr1:169898316..169900651-chr1:169903000..169904751,2	K562	blood:
33	chr1:169885836..169887922-chr1:169893783..169895856,2	MCF-7	breast:
34	chr1:169896264..169898992-chr1:170499654..170502527,2	MCF-7	breast:
35	chr1:169907968..169909649-chr1:169910615..169913475,2	K562	blood:
36	chr1:169891530..169894353-chr1:169899147..169901987,3	K562	blood:
37	chr1:169861783..169864814-chr1:169892837..169895451,3	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
ENSG00000075945	chromatin interactions
ENSG00000000457	chromatin interactions
ENSG00000120370	chromatin interactions
ENSG00000101144	chromatin interactions
ENSG00000231407	chromatin interactions

Extended variants
information (count: 1283 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:1283 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4519	chr1:169890574-169890575	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs559856517	chr1:169890583-169890584	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs144656623	chr1:169890599-169890600	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs549698923	chr1:169890617-169890618	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs567896336	chr1:169890621-169890622	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs7674	chr1:169890623-169890624	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs550323977	chr1:169890655-169890656	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs192958712	chr1:169890660-169890661	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs114938904	chr1:169890687-169890688	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs373947122	chr1:169890803-169890804	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs35534461	chr1:169890807-169890808	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs57164758	chr1:169890837-169890838	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs554145598	chr1:169890844-169890845	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs200602323	chr1:169890867-169890868	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs368164572	chr1:169890874-169890875	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs199699281	chr1:169890878-169890879	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs184581509	chr1:169890879-169890880	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs147987671	chr1:169890889-169890890	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs375270125	chr1:169890895-169890896	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs144868797	chr1:169890903-169890904	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs518928	chr1:169890933-169890934	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
22	rs188666389	chr1:169890967-169890968	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs372981273	chr1:169890970-169890971	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs45601233	chr1:169891012-169891013	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs544733595	chr1:169891038-169891039	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs201341273	chr1:169891056-169891057	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs3838393	chr1:169891057-169891058	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs397841367	chr1:169891066-169891067	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs201200148	chr1:169891068-169891069	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs571940213	chr1:169891103-169891104	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs192995233	chr1:169891131-169891132	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs374301026	chr1:169891190-169891191	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs561541733	chr1:169891231-169891232	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs548238411	chr1:169891243-169891244	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs532013334	chr1:169891252-169891253	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs550411795	chr1:169891316-169891317	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs565294409	chr1:169891332-169891333	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs532642135	chr1:169891347-169891348	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs568038413	chr1:169891390-169891391	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs533921292	chr1:169891407-169891408	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs547572535	chr1:169891491-169891492	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs566100861	chr1:169891626-169891627	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs536224885	chr1:169891630-169891631	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs548150857	chr1:169891640-169891641	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs74122429	chr1:169891668-169891669	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs74122430	chr1:169891675-169891676	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs185243260	chr1:169891693-169891694	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs555944677	chr1:169891776-169891777	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs189448005	chr1:169891777-169891778	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs490469	chr1:169891779-169891780	Weak transcription	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:407 , 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	chr1:169878400-169892200	Weak transcription	Duodenum Mucosa	Duodenum
3	chr1:169878400-169895200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
4	chr1:169878400-169946200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
5	chr1:169878600-169895000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
6	chr1:169880200-169892800	Weak transcription	Fetal Heart	heart
7	chr1:169881400-169901000	Weak transcription	Skeletal Muscle Female	skeletal muscle
8	chr1:169882200-169892000	Weak transcription	Brain Germinal Matrix	brain
9	chr1:169883000-169890600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
10	chr1:169884200-169913000	Weak transcription	Rectal Mucosa Donor 29	rectum
11	chr1:169884400-169891000	Weak transcription	Esophagus	oesophagus
12	chr1:169884600-169892800	Weak transcription	Pancreas	Pancrea
13	chr1:169884600-169895200	Weak transcription	Fetal Intestine Small	intestine
14	chr1:169884600-169900600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
15	chr1:169884600-169900600	Weak transcription	NHDF-Ad	bronchial
16	chr1:169885200-169900800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
17	chr1:169885400-169894000	Weak transcription	Right Ventricle	heart
18	chr1:169885400-169913200	Weak transcription	Ovary	ovary
19	chr1:169885600-169892200	Weak transcription	Brain Substantia Nigra	brain
20	chr1:169885600-169903200	Weak transcription	Placenta Amnion	Placenta Amnion
21	chr1:169885800-169896600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
22	chr1:169885800-169898000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
23	chr1:169886000-169894000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
24	chr1:169886400-169894600	Weak transcription	Primary B cells from cord blood	blood
25	chr1:169886400-169895200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
26	chr1:169886400-169913000	Weak transcription	Primary T cells fromperipheralblood	blood
27	chr1:169886600-169915600	Weak transcription	Stomach Smooth Muscle	stomach
28	chr1:169886800-169891000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
29	chr1:169887000-169911400	Weak transcription	Left Ventricle	heart
30	chr1:169888200-169891000	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
31	chr1:169888200-169891000	Strong transcription	Primary T helper cells fromperipheralblood	blood
32	chr1:169888200-169891000	Strong transcription	Adipose Nuclei	Adipose
33	chr1:169888400-169891000	Weak transcription	Brain Hippocampus Middle	brain
34	chr1:169888400-169892400	Weak transcription	Fetal Brain Male	brain
35	chr1:169888600-169891400	Weak transcription	Primary B cells from peripheral blood	blood
36	chr1:169888600-169891400	Weak transcription	Liver	Liver
37	chr1:169888800-169894800	Weak transcription	GM12878-XiMat	blood
38	chr1:169888800-169900600	Weak transcription	Fetal Stomach	stomach
39	chr1:169889000-169890800	Weak transcription	Fetal Muscle Trunk	muscle
40	chr1:169889000-169895200	Weak transcription	Duodenum Smooth Muscle	Duodenum
41	chr1:169889400-169891400	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
42	chr1:169889600-169900600	Weak transcription	Fetal Lung	lung
43	chr1:169889800-169898000	Weak transcription	Brain Inferior Temporal Lobe	brain
44	chr1:169890000-169890800	Strong transcription	Primary T helper cells PMA-I stimulated	--
45	chr1:169890200-169890800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
46	chr1:169890200-169891000	Strong transcription	Primary T cells from cord blood	blood
47	chr1:169890200-169895200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
48	chr1:169890800-169893600	Weak transcription	Psoas Muscle	Psoas
49	chr1:169890800-169894800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
50	chr1:169890800-169906200	Weak transcription	Primary T helper cells PMA-I stimulated	--

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