Variant report

Variant	nsv548187
Chromosome Location	chr1:169530837-169559035
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:655)
CpG islands
(count:489)
Chromatin interactive
region (count:15)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:655 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:169541178-169542037	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:169534688-169535455	HepG2	liver:	n/a	n/a
3	ARID3A	chr1:169553882-169554484	HepG2	liver:	n/a	n/a
4	ARID3A	chr1:169539100-169539788	HepG2	liver:	n/a	n/a
5	ARID3A	chr1:169557339-169558326	HepG2	liver:	n/a	n/a
6	ARID3A	chr1:169555576-169556383	HepG2	liver:	n/a	n/a
7	ARID3A	chr1:169537700-169538082	HepG2	liver:	n/a	n/a
8	ARID3A	chr1:169545546-169546227	HepG2	liver:	n/a	n/a
9	BHLHE40	chr1:169555793-169555821	K562	blood:	n/a	n/a
10	BHLHE40	chr1:169555531-169556131	HepG2	liver:	n/a	chr1:169555776-169555792
11	BHLHE40	chr1:169545709-169546119	HepG2	liver:	n/a	n/a
12	BRCA1	chr1:169555543-169556228	HepG2	liver:	n/a	n/a
13	CEBPB	chr1:169555556-169555899	HepG2	liver:	n/a	n/a
14	CEBPB	chr1:169557409-169557718	HepG2	liver:	n/a	chr1:169557645-169557656
15	CEBPB	chr1:169541501-169541833	HepG2	liver:	n/a	n/a
16	CEBPB	chr1:169534594-169534964	K562	blood:	n/a	chr1:169534774-169534785
17	CEBPB	chr1:169557480-169557715	HepG2	liver:	n/a	chr1:169557645-169557656
18	CEBPB	chr1:169534587-169534954	IMR90	lung:	n/a	chr1:169534774-169534785
19	CEBPB	chr1:169534622-169534947	H1-hESC	embryonic stem cell:	n/a	chr1:169534774-169534785
20	CEBPB	chr1:169534607-169534960	Hela-S3	cervix:	n/a	chr1:169534774-169534785
21	CEBPB	chr1:169534487-169535019	MCF-7	breast:	n/a	chr1:169534774-169534785
22	CEBPB	chr1:169534549-169535050	A549	lung:	n/a	chr1:169534774-169534785
23	CEBPB	chr1:169557411-169557791	HepG2	liver:	n/a	chr1:169557645-169557656
24	CEBPB	chr1:169557445-169557832	HepG2	liver:	n/a	chr1:169557645-169557656
25	CEBPB	chr1:169539310-169539666	HepG2	liver:	n/a	n/a
26	CEBPB	chr1:169534588-169534946	A549	lung:	n/a	chr1:169534774-169534785
27	CEBPB	chr1:169534530-169534891	HepG2	liver:	n/a	chr1:169534774-169534785
28	CEBPB	chr1:169539303-169539617	HepG2	liver:	n/a	n/a
29	CEBPB	chr1:169539347-169539662	HepG2	liver:	n/a	n/a
30	CEBPB	chr1:169539292-169539700	HepG2	liver:	n/a	n/a
31	CEBPB	chr1:169534594-169535003	HepG2	liver:	n/a	chr1:169534774-169534785
32	CEBPB	chr1:169534530-169534929	MCF-7	breast:	n/a	chr1:169534774-169534785
33	CEBPD	chr1:169555423-169555855	HepG2	liver:	n/a	n/a
34	CHD2	chr1:169555560-169556175	HepG2	liver:	n/a	n/a
35	CHD2	chr1:169555624-169555920	H1-hESC	embryonic stem cell:	n/a	n/a
36	CTCF	chr1:169555640-169555790	NHDF-neo	bronchial:	n/a	n/a
37	CTCF	chr1:169555680-169555830	GM12864	blood:	n/a	n/a
38	CTCF	chr1:169555680-169555830	SAEC	small airway:	n/a	n/a
39	CTCF	chr1:169555512-169555885	GM12892	blood:	n/a	chr1:169555637-169555650
40	CTCF	chr1:169555620-169555770	WI-38	lung:	n/a	chr1:169555637-169555650
41	CTCF	chr1:169555660-169555810	HEEpiC	esophagus:	n/a	n/a
42	CTCF	chr1:169555589-169555896	HepG2	liver:	n/a	chr1:169555637-169555650
43	CTCF	chr1:169556020-169556170	GM12872	blood:	n/a	n/a
44	CTCF	chr1:169555623-169555810	GM10248	blood:	n/a	chr1:169555637-169555650
45	CTCF	chr1:169556220-169556370	HepG2	liver:	n/a	n/a
46	CTCF	chr1:169555640-169555790	HMEC	breast:	n/a	n/a
47	CTCF	chr1:169555600-169555750	HCM	heart:	n/a	chr1:169555637-169555650
48	CTCF	chr1:169555760-169555910	HAc	cerebellar:	n/a	chr1:169555902-169555910
49	CTCF	chr1:169555513-169555940	H1-hESC	embryonic stem cell:	n/a	chr1:169555637-169555650 chr1:169555902-169555910
50	CTCF	chr1:169558140-169558290	Caco-2	colon:	n/a	n/a

(count:489 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:169556022-169556072	HMEC	breast:	n/a
2	chr1:169556022-169556072	HMEC	breast:	n/a
3	chr1:169556657-169556707	BJ	skin:	n/a
4	chr1:169556657-169556707	GM12892	blood:	n/a
5	chr1:169555805-169555855	NH-A	brain:	n/a
6	chr1:169555805-169555855	T-47D	breast:	n/a
7	chr1:169556022-169556072	HCM	heart:	n/a
8	chr1:169555674-169555724	Hepatocyte	liver:	n/a
9	chr1:169558925-169558975	HCF	heart:	n/a
10	chr1:169556022-169556072	HAEpiC	amniotic membrane:	n/a
11	chr1:169555674-169555724	AG10803	skin:	n/a
12	chr1:169555805-169555855	ECC-1	luminal epithelium:	n/a
13	chr1:169555805-169555855	IMR90	lung:	fetal
14	chr1:169558925-169558975	NT2-D1	testis:	n/a
15	chr1:169556657-169556707	ProgFib	skin:	n/a
16	chr1:169555674-169555724	NHDF-neo	bronchial:	n/a
17	chr1:169556657-169556707	HNPCEpiC	eye:	n/a
18	chr1:169555805-169555855	HEEpiC	esophagus:	n/a
19	chr1:169555681-169555731	HNPCEpiC	eye:	n/a
20	chr1:169555773-169555823	MCF10A-Er-Src	breast:	n/a
21	chr1:169555805-169555855	PrEC	prostate:	n/a
22	chr1:169555681-169555731	ECC-1	luminal epithelium:	n/a
23	chr1:169555674-169555724	HCF	heart:	n/a
24	chr1:169555805-169555855	AG10803	skin:	n/a
25	chr1:169555805-169555855	HCM	heart:	n/a
26	chr1:169555805-169555855	HRCEpiC	kidney:	n/a
27	chr1:169555773-169555823	GM12878	blood:	n/a
28	chr1:169555944-169555994	GM06990	blood:	n/a
29	chr1:169555944-169555994	HIPEpiC	eye:	n/a
30	chr1:169555805-169555855	RPTEC	kidney:	n/a
31	chr1:169556022-169556072	LNCaP	prostate:	n/a
32	chr1:169555674-169555724	AG04449	skin:	fetal
33	chr1:169556657-169556707	LNCaP	prostate:	n/a
34	chr1:169555773-169555823	Hepatocyte	liver:	n/a
35	chr1:169556022-169556072	GM19239	blood:	n/a
36	chr1:169556022-169556072	NHBE	bronchial:	n/a
37	chr1:169556657-169556707	T-47D	breast:	n/a
38	chr1:169555805-169555855	AG04450	lung:	fetal
39	chr1:169558925-169558975	HRPEpiC	eye:	n/a
40	chr1:169555805-169555855	HMEC	breast:	n/a
41	chr1:169558925-169558975	SK-N-SH_RA	brain:	n/a
42	chr1:169555674-169555724	NB4	blood:	n/a
43	chr1:169555681-169555731	IMR90	lung:	fetal
44	chr1:169556657-169556707	HIPEpiC	eye:	n/a
45	chr1:169558925-169558975	AG04449	skin:	fetal
46	chr1:169555674-169555724	PrEC	prostate:	n/a
47	chr1:169555674-169555724	HCT-116	colon:	n/a
48	chr1:169555773-169555823	AG10803	skin:	n/a
49	chr1:169556022-169556072	SAEC	small airway:	n/a
50	chr1:169555674-169555724	GM12892	blood:	n/a

(count:15 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:169541824..169543359-chr1:169543755..169546590,2	MCF-7	breast:
2	chr1:169531774..169534548-chr1:169536079..169538530,2	K562	blood:
3	chr1:169553531..169554398-chr1:169563651..169564307,2	MCF-7	breast:
4	chr1:169453485..169455825-chr1:169552064..169553822,2	K562	blood:
5	chr1:169543905..169545512-chr1:169548629..169550660,2	K562	blood:
6	chr1:169554006..169554804-chrX:81997894..81998531,2	MCF-7	breast:
7	chr1:169555910..169558714-chr1:169805893..169807663,2	K562	blood:
8	chr1:169529558..169531629-chr1:169534485..169537061,2	K562	blood:
9	chr1:169531774..169534548-chr1:169536079..169538530,2	K562	blood:
10	chr1:169541824..169543359-chr1:169543755..169546590,2	MCF-7	breast:
11	chr1:169539510..169541317-chr1:169543367..169545442,2	K562	blood:
12	chr1:169539510..169541317-chr1:169543367..169545442,2	K562	blood:
13	chr1:169529558..169531629-chr1:169534485..169537061,2	K562	blood:
14	chr1:169454435..169456317-chr1:169545578..169547535,2	MCF-7	breast:
15	chr1:169543905..169545512-chr1:169548629..169550660,2	K562	blood:

No data

Variant related genes	Relation type
F5	TF binding region
F5	CpG island
ENSG00000213062	chromatin interactions
ENSG00000117479	chromatin interactions

Extended variants
information (count: 1056 )
Associated
traits (count: 94 )

Variant overlapped rSNPs/rCNVs (count:1056 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1894702	chr1:169530837-169530838	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs550540694	chr1:169530846-169530847	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs562576919	chr1:169530929-169530930	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs541332366	chr1:169530951-169530952	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs564253334	chr1:169530967-169530968	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs3766119	chr1:169530981-169530982	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs567176994	chr1:169531006-169531007	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs552162872	chr1:169531023-169531024	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs3766120	chr1:169531035-169531036	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs534479478	chr1:169531065-169531066	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs75572965	chr1:169531081-169531082	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs3766121	chr1:169531085-169531086	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs3820061	chr1:169531135-169531136	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs556977366	chr1:169531151-169531152	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs112279055	chr1:169531266-169531267	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs371566236	chr1:169531288-169531289	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs191164515	chr1:169531316-169531317	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs369910651	chr1:169531403-169531404	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs539440672	chr1:169531404-169531405	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs528072164	chr1:169531405-169531406	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs7540556	chr1:169531442-169531443	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs559347593	chr1:169531443-169531444	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs573489239	chr1:169531444-169531445	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs369422967	chr1:169531452-169531453	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs561973631	chr1:169531459-169531460	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs533959514	chr1:169531486-169531487	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs147021901	chr1:169531498-169531499	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs544266523	chr1:169531555-169531556	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs4656690	chr1:169531571-169531572	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs533887429	chr1:169531581-169531582	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs137988418	chr1:169531587-169531588	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs533129575	chr1:169531601-169531602	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs34414085	chr1:169531650-169531651	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs567043694	chr1:169531701-169531702	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs551764520	chr1:169531719-169531720	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs571133323	chr1:169531741-169531742	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs564218066	chr1:169531760-169531761	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs184588641	chr1:169531789-169531790	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs538209092	chr1:169531795-169531796	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs556484094	chr1:169531885-169531886	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs138090477	chr1:169531989-169531990	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs535659897	chr1:169532007-169532008	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs550666789	chr1:169532017-169532018	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs111321535	chr1:169532047-169532048	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs375350725	chr1:169532050-169532051	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs35917495	chr1:169532094-169532095	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs539022753	chr1:169532106-169532107	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs10919192	chr1:169532111-169532112	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs10919193	chr1:169532159-169532160	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs534542904	chr1:169532167-169532168	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:94)

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
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Lung cancer	18438408	CNVD
Cancer	20164920	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:511 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:169505800-169534800	Weak transcription	Primary T helper cells PMA-I stimulated	--
2	chr1:169506200-169542800	Weak transcription	Right Ventricle	heart
3	chr1:169516000-169531400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr1:169518000-169531000	Strong transcription	HepG2	liver
5	chr1:169518400-169531000	Strong transcription	Liver	Liver
6	chr1:169524600-169541800	Weak transcription	Placenta	Placenta
7	chr1:169526600-169532200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
8	chr1:169528600-169533400	Weak transcription	Stomach Mucosa	stomach
9	chr1:169530200-169535400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
10	chr1:169530200-169539000	Weak transcription	Primary neutrophils fromperipheralblood	blood
11	chr1:169530400-169534000	Weak transcription	Primary monocytes fromperipheralblood	blood
12	chr1:169530800-169533200	Weak transcription	Monocytes-CD14+_RO01746	blood
13	chr1:169530800-169534800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
14	chr1:169531000-169532400	Weak transcription	Liver	Liver
15	chr1:169531000-169533000	Weak transcription	HepG2	liver
16	chr1:169531600-169534800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
17	chr1:169532400-169534600	Strong transcription	Liver	Liver
18	chr1:169533000-169533600	ZNF genes & repeats	HepG2	liver
19	chr1:169533200-169551600	Strong transcription	Monocytes-CD14+_RO01746	blood
20	chr1:169533400-169544600	Enhancers	Stomach Mucosa	stomach
21	chr1:169533600-169534200	Strong transcription	HepG2	liver
22	chr1:169534000-169541400	Strong transcription	Primary monocytes fromperipheralblood	blood
23	chr1:169534200-169534400	Bivalent Enhancer	Small Intestine	intestine
24	chr1:169534200-169537000	Genic enhancers	HepG2	liver
25	chr1:169534400-169536000	Enhancers	Duodenum Mucosa	Duodenum
26	chr1:169534600-169534800	Genic enhancers	Liver	Liver
27	chr1:169534600-169535800	Enhancers	HUVEC	blood vessel
28	chr1:169534600-169537400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
29	chr1:169534800-169535200	Enhancers	Primary hematopoietic stem cells	blood
30	chr1:169534800-169535400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
31	chr1:169534800-169535400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
32	chr1:169534800-169535600	Enhancers	Primary T regulatory cells fromperipheralblood	blood
33	chr1:169534800-169535600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
34	chr1:169534800-169535600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
35	chr1:169534800-169535600	Enhancers	Dnd41	blood
36	chr1:169534800-169535800	Enhancers	Primary T helper cells PMA-I stimulated	--
37	chr1:169534800-169535800	Enhancers	NHEK	skin
38	chr1:169534800-169538800	Enhancers	Liver	Liver
39	chr1:169535000-169535600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
40	chr1:169535000-169535600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
41	chr1:169535000-169535600	Enhancers	Thymus	Thymus
42	chr1:169535000-169535800	Enhancers	Fetal Kidney	kidney
43	chr1:169535000-169535800	Enhancers	HMEC	breast
44	chr1:169535200-169535600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
45	chr1:169535200-169535600	Enhancers	Rectal Mucosa Donor 31	rectum
46	chr1:169535200-169535800	Enhancers	Primary T helper naive cells from peripheral blood	blood
47	chr1:169535200-169535800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
48	chr1:169535400-169535600	Genic enhancers	Primary T helper 17 cells PMA-I stimulated	--
49	chr1:169535400-169540200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
50	chr1:169535600-169536000	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--

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