Variant report

Variant	nsv872549
Chromosome Location	chr1:173509586-173546835
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:289)
CpG islands
(count:123)
Chromatin interactive
region (count:9)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:289 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr1:173523218-173523577	K562	blood:	n/a	n/a
2	BHLHE40	chr1:173539874-173539908	GM12878	blood:	n/a	n/a
3	BHLHE40	chr1:173524875-173525146	K562	blood:	n/a	chr1:173524988-173524997 chr1:173524989-173524998 chr1:173524983-173525004 chr1:173524987-173525000 chr1:173524989-173524998
4	CEBPB	chr1:173541627-173541979	K562	blood:	n/a	chr1:173541795-173541806
5	CEBPB	chr1:173541654-173541978	IMR90	lung:	n/a	chr1:173541795-173541806
6	CEBPB	chr1:173523317-173523585	K562	blood:	n/a	n/a
7	CEBPB	chr1:173541667-173541921	Hela-S3	cervix:	n/a	chr1:173541795-173541806
8	CEBPB	chr1:173541658-173541998	A549	lung:	n/a	chr1:173541795-173541806
9	CEBPB	chr1:173541624-173541988	HepG2	liver:	n/a	chr1:173541795-173541806
10	CEBPB	chr1:173523295-173523576	K562	blood:	n/a	n/a
11	CEBPB	chr1:173517672-173517836	K562	blood:	n/a	n/a
12	CEBPB	chr1:173542774-173543026	A549	lung:	n/a	n/a
13	CHD1	chr1:173539918-173539925	GM12878	blood:	n/a	n/a
14	CHD2	chr1:173523318-173523618	K562	blood:	n/a	n/a
15	CHD2	chr1:173532109-173532160	H1-hESC	embryonic stem cell:	n/a	n/a
16	CTCF	chr1:173539786-173539974	GM12878	blood:	n/a	n/a
17	CTCF	chr1:173514920-173515070	HCPEpiC	choroid plexus:	n/a	n/a
18	CTCF	chr1:173532180-173532330	HFF-Myc	foreskin:	n/a	n/a
19	CTCF	chr1:173532080-173532230	HCFaa	heart:	n/a	chr1:173532140-173532149
20	CTCF	chr1:173532080-173532230	AG04449	skin:	n/a	chr1:173532140-173532149
21	CTCF	chr1:173532020-173532170	GM12873	blood:	n/a	chr1:173532140-173532149
22	CTCF	chr1:173532100-173532250	AG04450	lung:	n/a	chr1:173532140-173532149
23	CTCF	chr1:173514970-173515102	K562	blood:	n/a	n/a
24	CTCF	chr1:173515015-173515036	Hela-S3	cervix:	n/a	n/a
25	CTCF	chr1:173532060-173532210	K562	blood:	n/a	chr1:173532140-173532149
26	CTCF	chr1:173514550-173514589	ProgFib	skin:	n/a	n/a
27	CTCF	chr1:173532040-173532190	RPTEC	kidney:	n/a	chr1:173532140-173532149
28	CTCF	chr1:173514840-173514990	HCT-116	colon:	n/a	n/a
29	CTCF	chr1:173532080-173532230	HPAF	blood vessel:	n/a	chr1:173532140-173532149
30	CTCF	chr1:173514992-173515052	HepG2	liver:	n/a	n/a
31	CTCF	chr1:173532040-173532190	HPF	lung:	n/a	chr1:173532140-173532149
32	CTCF	chr1:173531980-173532130	AG04449	skin:	n/a	n/a
33	CTCF	chr1:173532040-173532190	MCF-7	breast:	n/a	chr1:173532140-173532149
34	CTCF	chr1:173532060-173532210	HBMEC	blood vessel:	n/a	chr1:173532140-173532149
35	CTCF	chr1:173515000-173515150	RPTEC	kidney:	n/a	n/a
36	CTCF	chr1:173532084-173532225	Fibrobl	skin:	n/a	chr1:173532140-173532149
37	CTCF	chr1:173531960-173532110	RPTEC	kidney:	n/a	n/a
38	CTCF	chr1:173514960-173515110	HEEpiC	esophagus:	n/a	n/a
39	CTCF	chr1:173532100-173532250	HMF	breast:	n/a	chr1:173532140-173532149
40	CTCF	chr1:173532091-173532207	ProgFib	skin:	n/a	chr1:173532140-173532149
41	CTCF	chr1:173532060-173532210	Caco-2	colon:	n/a	chr1:173532140-173532149
42	CTCF	chr1:173514960-173515110	K562	blood:	n/a	n/a
43	CTCF	chr1:173532100-173532250	HEK293	kidney:	n/a	chr1:173532140-173532149
44	CTCF	chr1:173519454-173519504	Fibrobl	skin:	n/a	n/a
45	CTCF	chr1:173514940-173515090	HCPEpiC	choroid plexus:	n/a	n/a
46	CTCF	chr1:173532080-173532230	HFF	foreskin:	n/a	chr1:173532140-173532149
47	CTCF	chr1:173528440-173528590	MCF-7	breast:	n/a	n/a
48	CTCF	chr1:173532020-173532170	BE2_C	brain:	n/a	chr1:173532140-173532149
49	CTCF	chr1:173532200-173532350	WERI-Rb-1	eye:	n/a	n/a
50	CTCF	chr1:173532060-173532210	SK-N-SH_RA	brain:	n/a	chr1:173532140-173532149

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:173546325-173546375	LNCaP	prostate:	n/a
2	chr1:173546325-173546375	LNCaP	prostate:	n/a
3	chr1:173517966-173518016	NT2-D1	testis:	n/a
4	chr1:173546325-173546375	HNPCEpiC	eye:	n/a
5	chr1:173517966-173518016	HPAEpiC	pulmonary alveolar:	n/a
6	chr1:173546325-173546375	PANC-1	pancreas:	n/a
7	chr1:173546325-173546375	MCF-7	breast:	n/a
8	chr1:173517966-173518016	HIPEpiC	eye:	n/a
9	chr1:173517966-173518016	HCF	heart:	n/a
10	chr1:173546325-173546375	HUVEC	blood vessel:	n/a
11	chr1:173517966-173518016	HepG2	liver:	n/a
12	chr1:173546325-173546375	SK-N-SH	brain:	n/a
13	chr1:173546325-173546375	HCT-116	colon:	n/a
14	chr1:173546325-173546375	HPAEpiC	pulmonary alveolar:	n/a
15	chr1:173546325-173546375	H1-hESC	embryonic stem cell:	embryo
16	chr1:173546325-173546375	HEK293	kidney:	embryo
17	chr1:173546325-173546375	SK-N-MC	brain:	n/a
18	chr1:173546325-173546375	AoSMC	blood vessel:	n/a
19	chr1:173517966-173518016	HNPCEpiC	eye:	n/a
20	chr1:173546325-173546375	HRPEpiC	eye:	n/a
21	chr1:173546325-173546375	NHDF-neo	bronchial:	n/a
22	chr1:173517966-173518016	HAEpiC	amniotic membrane:	n/a
23	chr1:173517966-173518016	MCF10A-Er-Src	breast:	n/a
24	chr1:173546325-173546375	A549	lung:	n/a
25	chr1:173517966-173518016	LNCaP	prostate:	n/a
26	chr1:173517966-173518016	PrEC	prostate:	n/a
27	chr1:173546325-173546375	SAEC	small airway:	n/a
28	chr1:173546325-173546375	RPTEC	kidney:	n/a
29	chr1:173546325-173546375	HAEpiC	amniotic membrane:	n/a
30	chr1:173517966-173518016	Hela-S3	cervix:	n/a
31	chr1:173546325-173546375	HRE	kidney:	n/a
32	chr1:173546325-173546375	ovcar-3	ovarian:	n/a
33	chr1:173546325-173546375	SK-N-SH_RA	brain:	n/a
34	chr1:173517966-173518016	PANC-1	pancreas:	n/a
35	chr1:173546325-173546375	MCF10A-Er-Src	breast:	n/a
36	chr1:173546325-173546375	HL-60	blood:	n/a
37	chr1:173546325-173546375	Caco-2	colon:	n/a
38	chr1:173546325-173546375	HEEpiC	esophagus:	n/a
39	chr1:173546325-173546375	BE2_C	brain:	n/a
40	chr1:173517966-173518016	HCM	heart:	n/a
41	chr1:173546325-173546375	NB4	blood:	n/a
42	chr1:173517966-173518016	HRCEpiC	kidney:	n/a
43	chr1:173517966-173518016	AG10803	skin:	n/a
44	chr1:173517966-173518016	HCT-116	colon:	n/a
45	chr1:173546325-173546375	T-47D	breast:	n/a
46	chr1:173546325-173546375	GM12878	blood:	n/a
47	chr1:173517966-173518016	HL-60	blood:	n/a
48	chr1:173517966-173518016	AG09309	skin:	n/a
49	chr1:173517966-173518016	AG04450	lung:	fetal
50	chr1:173546325-173546375	HCPEpiC	choroid plexus:	n/a

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:173526861..173529364-chr1:173529835..173532610,2	MCF-7	breast:
2	chr1:173539762..173541547-chr1:173573962..173575508,2	K562	blood:
3	chr1:173529588..173531348-chr1:173534386..173536103,2	K562	blood:
4	chr1:173546698..173549628-chr1:173553244..173556052,2	K562	blood:
5	chr1:173521720..173523239-chr1:173523981..173526705,2	MCF-7	breast:
6	chr1:173475650..173476359-chr1:173514574..173515395,2	MCF-7	breast:
7	chr1:173539981..173542937-chr1:173592354..173595230,2	MCF-7	breast:
8	chr1:173529588..173531348-chr1:173534386..173536103,2	K562	blood:
9	chr1:173526861..173529364-chr1:173529835..173532610,2	MCF-7	breast:

No data

Variant related genes	Relation type
SLC9C2	TF binding region
ENSG00000238272	TF binding region
SLC9C2	CpG island
ENSG00000238272	CpG island
ENSG00000238272	chromatin interactions

Extended variants
information (count: 743 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:743 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7520814	chr1:173509586-173509587	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs189909983	chr1:173509592-173509593	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs558592945	chr1:173509623-173509624	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs577098799	chr1:173509630-173509631	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs577049482	chr1:173509688-173509689	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs180764532	chr1:173509758-173509759	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs145796161	chr1:173509797-173509798	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs577548862	chr1:173516616-173516617	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs16846204	chr1:173516663-173516664	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs559936422	chr1:173516703-173516704	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs374848574	chr1:173516774-173516775	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs371358577	chr1:173516799-173516800	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs144358733	chr1:173516815-173516816	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs548355015	chr1:173516826-173516827	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs200859968	chr1:173516856-173516857	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs16846206	chr1:173516871-173516872	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs10494490	chr1:173516903-173516904	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs140112573	chr1:173516907-173516908	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs201198709	chr1:173516909-173516910	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs114115413	chr1:173516915-173516916	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs115601744	chr1:173516931-173516932	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs36011264	chr1:173517051-173517052	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs369373002	chr1:173517054-173517055	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs541561488	chr1:173517066-173517067	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs188702652	chr1:173517074-173517075	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs567854564	chr1:173517085-173517086	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs535545182	chr1:173517096-173517097	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs556733127	chr1:173517143-173517144	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs150925462	chr1:173517233-173517234	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs560492427	chr1:173517322-173517323	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs539047398	chr1:173517330-173517331	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs570195309	chr1:173517348-173517349	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs180749779	chr1:173517390-173517391	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs147799683	chr1:173517468-173517469	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs541688777	chr1:173517471-173517472	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs6425247	chr1:173517540-173517541	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs369566180	chr1:173517546-173517547	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs7551131	chr1:173517547-173517548	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs553307750	chr1:173517567-173517568	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs372554705	chr1:173517581-173517582	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs267598169	chr1:173517590-173517591	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs267598170	chr1:173517608-173517609	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs114617044	chr1:173517632-173517633	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs200862414	chr1:173517635-173517636	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs563596482	chr1:173517689-173517690	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs549648145	chr1:173517726-173517727	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs369516375	chr1:173517738-173517739	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs566383030	chr1:173517764-173517765	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs530966846	chr1:173517814-173517815	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs200231892	chr1:173517844-173517845	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:92)

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
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
Glioblastoma multiforme	21080181	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
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
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Developmental delay	21147756	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21509527	CNVD
Glioblastoma multiforme	17369134	CNVD
Cancer	17440070	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:79 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:173508600-173509800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
2	chr1:173508600-173509800	Enhancers	Adipose Nuclei	Adipose
3	chr1:173516600-173523600	Enhancers	Primary T helper cells PMA-I stimulated	--
4	chr1:173516800-173517400	Enhancers	Primary T regulatory cells fromperipheralblood	blood
5	chr1:173517000-173517400	Enhancers	Primary T helper naive cells from peripheral blood	blood
6	chr1:173517200-173517800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr1:173517200-173523000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
8	chr1:173517400-173518000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
9	chr1:173517400-173518600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
10	chr1:173517400-173518600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
11	chr1:173518000-173518600	Enhancers	iPS-15b Cell Line	embryonic stem cell
12	chr1:173518000-173523800	Enhancers	Primary T helper cells fromperipheralblood	blood
13	chr1:173518200-173519800	Enhancers	HUVEC	blood vessel
14	chr1:173518200-173523600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
15	chr1:173518400-173519600	Enhancers	Primary T killer memory cells from peripheral blood	blood
16	chr1:173518400-173522600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
17	chr1:173518400-173523400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
18	chr1:173518600-173522800	Enhancers	Primary T regulatory cells fromperipheralblood	blood
19	chr1:173518600-173523000	Enhancers	Primary T helper naive cells from peripheral blood	blood
20	chr1:173519000-173519200	Enhancers	K562	blood
21	chr1:173519000-173521200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
22	chr1:173519000-173522800	Enhancers	Primary T cells from cord blood	blood
23	chr1:173519000-173523600	Enhancers	Primary T cells fromperipheralblood	blood
24	chr1:173519200-173520200	Weak transcription	K562	blood
25	chr1:173519200-173521000	Enhancers	Dnd41	blood
26	chr1:173519600-173520000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
27	chr1:173519800-173520200	Weak transcription	HUVEC	blood vessel
28	chr1:173519800-173521800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
29	chr1:173520000-173520400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
30	chr1:173520000-173521000	Enhancers	Primary hematopoietic stem cells short term culture	blood
31	chr1:173520000-173521400	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
32	chr1:173520000-173523600	Enhancers	Primary T killer memory cells from peripheral blood	blood
33	chr1:173520200-173520400	Enhancers	HUVEC	blood vessel
34	chr1:173520200-173520600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
35	chr1:173520200-173520600	Enhancers	K562	blood
36	chr1:173520400-173523400	Weak transcription	HUVEC	blood vessel
37	chr1:173520600-173523000	Weak transcription	K562	blood
38	chr1:173521000-173523400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
39	chr1:173523000-173523200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
40	chr1:173523000-173523800	Enhancers	K562	blood
41	chr1:173523200-173523600	Enhancers	Primary T helper naive cells from peripheral blood	blood
42	chr1:173523200-173524400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
43	chr1:173523200-173525200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
44	chr1:173523200-173525400	Enhancers	HMEC	breast
45	chr1:173523200-173525400	Enhancers	NHEK	skin
46	chr1:173523200-173525600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
47	chr1:173523200-173525600	Enhancers	Hela-S3	cervix
48	chr1:173523400-173523600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
49	chr1:173523400-173524000	Enhancers	Primary hematopoietic stem cells short term culture	blood
50	chr1:173523400-173525400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin

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