Variant report

Variant	nsv517826
Chromosome Location	chr1:161263380-161277601
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:440)
CpG islands
(count:123)
Chromatin interactive
region (count:18)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:2)

(count:440 , 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	chr1:161277187-161277314	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:161276098-161276150	HepG2	liver:	n/a	n/a
3	ARID3A	chr1:161277171-161277388	K562	blood:	n/a	n/a
4	ATF2	chr1:161274746-161275106	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr1:161275755-161276344	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr1:161274689-161275055	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr1:161276064-161276346	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr1:161277147-161277511	K562	blood:	n/a	n/a
9	BCL11A	chr1:161267983-161268244	GM12878	blood:	n/a	n/a
10	BHLHE40	chr1:161277135-161277353	K562	blood:	n/a	n/a
11	BHLHE40	chr1:161267991-161268191	GM12878	blood:	n/a	n/a
12	BHLHE40	chr1:161276011-161276365	K562	blood:	n/a	n/a
13	BRCA1	chr1:161276127-161276343	H1-hESC	embryonic stem cell:	n/a	n/a
14	CBX3	chr1:161276609-161277536	K562	blood:	n/a	n/a
15	CBX3	chr1:161275715-161276424	K562	blood:	n/a	n/a
16	CCNT2	chr1:161275840-161276276	K562	blood:	n/a	chr1:161276089-161276098
17	CCNT2	chr1:161276869-161277392	K562	blood:	n/a	n/a
18	CEBPB	chr1:161275816-161276306	H1-hESC	embryonic stem cell:	n/a	chr1:161275930-161275941
19	CEBPB	chr1:161275756-161276073	IMR90	lung:	n/a	chr1:161275930-161275941
20	CEBPB	chr1:161275740-161276120	K562	blood:	n/a	chr1:161275930-161275941
21	CEBPB	chr1:161275807-161276085	HepG2	liver:	n/a	chr1:161275930-161275941
22	CEBPB	chr1:161275791-161276062	K562	blood:	n/a	chr1:161275930-161275941
23	CEBPB	chr1:161263581-161263660	K562	blood:	n/a	n/a
24	CEBPB	chr1:161274860-161274980	K562	blood:	n/a	n/a
25	CEBPB	chr1:161275743-161276105	K562	blood:	n/a	chr1:161275930-161275941
26	CHD2	chr1:161274805-161274888	GM12878	blood:	n/a	n/a
27	CHD2	chr1:161277149-161277349	K562	blood:	n/a	n/a
28	CHD2	chr1:161275681-161276282	H1-hESC	embryonic stem cell:	n/a	n/a
29	CHD2	chr1:161275763-161276290	K562	blood:	n/a	n/a
30	CHD2	chr1:161275714-161276288	GM12878	blood:	n/a	n/a
31	CREB1	chr1:161275611-161276384	H1-hESC	embryonic stem cell:	n/a	n/a
32	CREB1	chr1:161275809-161276469	H1-hESC	embryonic stem cell:	n/a	n/a
33	CREB1	chr1:161275676-161276467	HepG2	liver:	n/a	n/a
34	CTCF	chr1:161276120-161276270	GM12871	blood:	n/a	n/a
35	CTCF	chr1:161276140-161276290	GM12872	blood:	n/a	n/a
36	CTCF	chr1:161276040-161276190	RPTEC	kidney:	n/a	n/a
37	CTCF	chr1:161276165-161276283	HUVEC	blood vessel:	n/a	n/a
38	CTCF	chr1:161276140-161276290	NHDF-neo	bronchial:	n/a	n/a
39	CTCF	chr1:161276100-161276250	GM12868	blood:	n/a	n/a
40	CTCF	chr1:161276120-161276270	AG04449	skin:	n/a	n/a
41	CTCF	chr1:161276120-161276270	GM12872	blood:	n/a	n/a
42	CTCF	chr1:161276120-161276270	GM12866	blood:	n/a	n/a
43	CTCF	chr1:161276100-161276250	HUVEC	blood vessel:	n/a	n/a
44	CTCF	chr1:161276100-161276250	HFF	foreskin:	n/a	n/a
45	CTCF	chr1:161276120-161276270	BJ	skin:	n/a	n/a
46	CTCF	chr1:161276067-161276343	GM19238	blood:	n/a	n/a
47	CTCF	chr1:161276200-161276350	BE2_C	brain:	n/a	n/a
48	CTCF	chr1:161276120-161276270	HUVEC	blood vessel:	n/a	n/a
49	CTCF	chr1:161275869-161275893	Lung_OC	lung:	n/a	n/a
50	CTCF	chr1:161276102-161276293	Pancreas_OC	pancreas:	n/a	n/a

(count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:161275561-161275611	Hela-S3	cervix:	n/a
2	chr1:161275561-161275611	Hela-S3	cervix:	n/a
3	chr1:161276204-161276254	AG09319	gingival:	n/a
4	chr1:161276204-161276254	Hepatocyte	liver:	n/a
5	chr1:161276204-161276254	HRPEpiC	eye:	n/a
6	chr1:161276204-161276254	GM19239	blood:	n/a
7	chr1:161276204-161276254	CMK	blood:	n/a
8	chr1:161276204-161276254	RPTEC	kidney:	n/a
9	chr1:161276204-161276254	PFSK-1	brain:	n/a
10	chr1:161275561-161275611	AG04450	lung:	fetal
11	chr1:161275561-161275611	PFSK-1	brain:	n/a
12	chr1:161276204-161276254	HNPCEpiC	eye:	n/a
13	chr1:161276204-161276254	SKMC	muscle:	n/a
14	chr1:161275561-161275611	NHDF-neo	bronchial:	n/a
15	chr1:161275561-161275611	ProgFib	skin:	n/a
16	chr1:161276204-161276254	HMEC	breast:	n/a
17	chr1:161276204-161276254	NHBE	bronchial:	n/a
18	chr1:161275561-161275611	Caco-2	colon:	n/a
19	chr1:161276204-161276254	SAEC	small airway:	n/a
20	chr1:161276204-161276254	SK-N-MC	brain:	n/a
21	chr1:161276204-161276254	SK-N-SH	brain:	n/a
22	chr1:161276204-161276254	AG10803	skin:	n/a
23	chr1:161275561-161275611	MCF-7	breast:	n/a
24	chr1:161275561-161275611	LNCaP	prostate:	n/a
25	chr1:161276204-161276254	HRE	kidney:	n/a
26	chr1:161276204-161276254	HEK293	kidney:	embryo
27	chr1:161275561-161275611	MCF10A-Er-Src	breast:	n/a
28	chr1:161276204-161276254	HUVEC	blood vessel:	n/a
29	chr1:161276204-161276254	A549	lung:	n/a
30	chr1:161276204-161276254	NB4	blood:	n/a
31	chr1:161276204-161276254	IMR90	lung:	fetal
32	chr1:161275561-161275611	IMR90	lung:	fetal
33	chr1:161276204-161276254	K562	blood:	n/a
34	chr1:161275561-161275611	BE2_C	brain:	n/a
35	chr1:161276204-161276254	MCF10A-Er-Src	breast:	n/a
36	chr1:161276204-161276254	ECC-1	luminal epithelium:	n/a
37	chr1:161276204-161276254	HPAEpiC	pulmonary alveolar:	n/a
38	chr1:161276204-161276254	GM12891	blood:	n/a
39	chr1:161276204-161276254	AG04449	skin:	fetal
40	chr1:161275561-161275611	SKMC	muscle:	n/a
41	chr1:161275561-161275611	SK-N-SH	brain:	n/a
42	chr1:161275561-161275611	NB4	blood:	n/a
43	chr1:161275561-161275611	HPAEpiC	pulmonary alveolar:	n/a
44	chr1:161275561-161275611	ovcar-3	ovarian:	n/a
45	chr1:161275561-161275611	HEEpiC	esophagus:	n/a
46	chr1:161275561-161275611	SK-N-SH_RA	brain:	n/a
47	chr1:161276204-161276254	HepG2	liver:	n/a
48	chr1:161275561-161275611	A549	lung:	n/a
49	chr1:161276204-161276254	ProgFib	skin:	n/a
50	chr1:161276204-161276254	HIPEpiC	eye:	n/a

(count:18 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:161195815..161198746-chr1:161267271..161268897,2	K562	blood:
2	chr1:161255642..161257216-chr1:161264008..161266432,2	K562	blood:
3	chr1:161263327..161265806-chr1:161269282..161270908,2	K562	blood:
4	chr1:161275235..161277911-chr1:161283525..161285261,2	MCF-7	breast:
5	chr1:161167464..161169651-chr1:161275959..161277953,2	K562	blood:
6	chr1:161122555..161125252-chr1:161276427..161278072,2	K562	blood:
7	chr1:161195862..161198260-chr1:161276077..161278142,2	K562	blood:
8	chr1:161194395..161196017-chr1:161272976..161274680,2	K562	blood:
9	chr1:161150561..161152446-chr1:161277325..161279650,2	K562	blood:
10	chr1:161266985..161268889-chr1:161273445..161276063,2	K562	blood:
11	chr1:161252880..161255836-chr1:161273696..161275808,2	MCF-7	breast:
12	chr1:161196949..161197777-chr1:161276110..161277146,3	K562	blood:
13	chr1:161269161..161270798-chr1:161282887..161284845,2	MCF-7	breast:
14	chr1:161178175..161181614-chr1:161276082..161277879,3	K562	blood:
15	chr1:161192625..161198260-chr1:161274899..161278564,8	K562	blood:
16	chr1:161263327..161265806-chr1:161269282..161270908,2	K562	blood:
17	chr1:161269370..161272593-chr1:161272649..161275995,5	K562	blood:
18	chr1:161273354..161275189-chr1:161279747..161282095,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PCP4L1-1	chr1:161265855-161266179	XLOC_000440
2	lnc-PCP4L1-1	chr1:161265664-161265702	XLOC_000440

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	MPZ	hsa-miR-192-5p	chr1:161274737-161274757
2	MPZ	hsa-miR-215-5p	chr1:161274737-161274757

Variant related genes	Relation type
MPZ	TF binding region
MPZ	CpG island
ENSG00000143252	chromatin interactions
ENSG00000158859	chromatin interactions
ENSG00000158864	chromatin interactions
ENSG00000158874	chromatin interactions
ENSG00000263548	chromatin interactions
ENSG00000158887	chromatin interactions
ENSG00000143222	chromatin interactions
ENSG00000158882	chromatin interactions

Extended variants
information (count: 554 )
Associated
traits (count: 109 )

Variant overlapped rSNPs/rCNVs (count:554 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12093075	chr1:161263380-161263381	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs566899990	chr1:161263418-161263419	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs143957387	chr1:161263491-161263492	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs190569621	chr1:161263495-161263496	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs372164664	chr1:161263514-161263515	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs569462316	chr1:161263523-161263524	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs374891817	chr1:161263541-161263542	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs540567984	chr1:161263554-161263555	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs78635517	chr1:161263599-161263600	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs181970234	chr1:161263635-161263636	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs146426519	chr1:161263636-161263637	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs115073149	chr1:161263646-161263647	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs552669394	chr1:161263648-161263649	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs113230634	chr1:161263660-161263661	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs544614332	chr1:161263677-161263678	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs114222137	chr1:161263693-161263694	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs544386880	chr1:161263788-161263789	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs560960533	chr1:161263851-161263852	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs150173464	chr1:161263911-161263912	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs540702529	chr1:161263920-161263921	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs560586549	chr1:161263953-161263954	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs573187008	chr1:161263956-161263957	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs375220234	chr1:161263970-161263971	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs552609700	chr1:161263978-161263979	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs563195826	chr1:161264012-161264013	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs34362626	chr1:161264031-161264032	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs548739743	chr1:161264056-161264057	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs148885119	chr1:161264068-161264069	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs534137915	chr1:161264075-161264076	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs562556220	chr1:161264090-161264091	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs76998923	chr1:161264100-161264101	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs368316622	chr1:161264138-161264139	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs546249043	chr1:161264139-161264140	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs146525903	chr1:161264165-161264166	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs4587585	chr1:161264180-161264181	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs143113186	chr1:161264201-161264202	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs371815861	chr1:161264211-161264212	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs575480966	chr1:161264212-161264213	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs537779454	chr1:161264221-161264222	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs554871229	chr1:161264224-161264225	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs574654505	chr1:161264371-161264372	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs116664052	chr1:161264385-161264386	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs560526592	chr1:161264388-161264389	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs114118036	chr1:161264398-161264399	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs76053929	chr1:161264442-161264443	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs76262089	chr1:161264443-161264444	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs574065847	chr1:161264498-161264499	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs186174146	chr1:161264513-161264514	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs562769633	chr1:161264572-161264573	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs190603157	chr1:161264589-161264590	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:109)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Liposarcoma	21253554	CNVD
Non-small cell lung cancer	21385341	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Cervical cancer	21062161	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	21183584	CNVD
Multiple myeloma	16461302	CNVD
Lung cancer	18438408	CNVD
Rett syndrome	21593744	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Systemic lupus erythematosus	21956041	CNVD
Non-syndromic sensorineural hearing loss	15273396	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
Breast cancer	17899364	CNVD
Bladder cancer	19088036	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Retinoblastoma	19183342	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Type 2 diabetes	19141583	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
Bladder cancer	21909424	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
low-grade B-cell lymphoma tumor	18367492	CNVD
Breast cancer	21611746	CNVD
Neuroblastoma	18923191	CNVD
Systemic lupus erythematosus	19220326	CNVD
Systemic lupus erythematosus	19287148	CNVD
Glomerulonephritis	19341492	CNVD
Systemic lupus erythematosus	18559452	CNVD
Systemic autoimmune disease	17597778	CNVD
Glomerulonephritis	17008540	CNVD
Glomerulonephritis	16482158	CNVD
Soft tissue tumor	16732325	CNVD
Cancer	17060936	CNVD
Lung cancer	16740712	CNVD
Breast cancer	21045282	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Follicular lymphoma	18703704	CNVD
Myelofibrosis	22110671	CNVD
Intracranial ependymoma	16609018	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	20409316	CNVD
Mental retardation	17847001	CNVD
Idiopathic thrombocytopenic purpura	17827395	CNVD
Pancreatic cancer	17952125	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:696 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:161243200-161264000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
2	chr1:161250400-161274200	Weak transcription	Fetal Stomach	stomach
3	chr1:161252400-161274800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
4	chr1:161255200-161274800	Weak transcription	Lung	lung
5	chr1:161255600-161274600	Weak transcription	Adipose Nuclei	Adipose
6	chr1:161256400-161272800	Weak transcription	Primary T cells from cord blood	blood
7	chr1:161259000-161267400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr1:161260200-161265600	Weak transcription	HepG2	liver
9	chr1:161261000-161272800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
10	chr1:161261400-161273200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
11	chr1:161261400-161273800	Weak transcription	Fetal Intestine Small	intestine
12	chr1:161261600-161274200	Weak transcription	Fetal Intestine Large	intestine
13	chr1:161263200-161274600	Weak transcription	Placenta	Placenta
14	chr1:161265600-161265800	Enhancers	Brain Angular Gyrus	brain
15	chr1:161265600-161266000	Enhancers	HepG2	liver
16	chr1:161265800-161273600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
17	chr1:161266200-161273800	Weak transcription	Primary T helper cells PMA-I stimulated	--
18	chr1:161266600-161269800	Enhancers	Primary monocytes fromperipheralblood	blood
19	chr1:161266800-161267000	Enhancers	Primary B cells from cord blood	blood
20	chr1:161266800-161267400	Enhancers	Monocytes-CD14+_RO01746	blood
21	chr1:161266800-161268400	Enhancers	Primary neutrophils fromperipheralblood	blood
22	chr1:161267000-161268400	Enhancers	Primary B cells from peripheral blood	blood
23	chr1:161267000-161273200	Weak transcription	Primary B cells from cord blood	blood
24	chr1:161267200-161267800	Enhancers	Brain Hippocampus Middle	brain
25	chr1:161267400-161267600	Enhancers	Primary hematopoietic stem cells	blood
26	chr1:161267400-161268000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
27	chr1:161267400-161268200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
28	chr1:161267400-161268200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
29	chr1:161267400-161268200	Enhancers	GM12878-XiMat	blood
30	chr1:161267600-161269400	Enhancers	Primary hematopoietic stem cells short term culture	blood
31	chr1:161267600-161273800	Weak transcription	Primary hematopoietic stem cells	blood
32	chr1:161267800-161268200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
33	chr1:161268000-161269400	Enhancers	Monocytes-CD14+_RO01746	blood
34	chr1:161268200-161269200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
35	chr1:161268200-161269200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr1:161268200-161272600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
37	chr1:161268200-161273800	Weak transcription	GM12878-XiMat	blood
38	chr1:161268400-161272000	Weak transcription	Primary neutrophils fromperipheralblood	blood
39	chr1:161268400-161272800	Weak transcription	Primary B cells from peripheral blood	blood
40	chr1:161269000-161269200	Weak transcription	HUES48 Cell Line	embryonic stem cell
41	chr1:161269000-161271200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
42	chr1:161269000-161272800	Weak transcription	Primary T helper cells fromperipheralblood	blood
43	chr1:161269000-161273200	Weak transcription	HUES6 Cell Line	embryonic stem cell
44	chr1:161269200-161269400	Enhancers	H1 Cell Line	embryonic stem cell
45	chr1:161269200-161269400	Enhancers	HUES48 Cell Line	embryonic stem cell
46	chr1:161269200-161269400	Enhancers	iPS-18 Cell Line	embryonic stem cell
47	chr1:161269200-161269600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
48	chr1:161269200-161269600	Enhancers	HUVEC	blood vessel
49	chr1:161269200-161269800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
50	chr1:161269200-161269800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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