Variant report

Variant	nsv1006200
Chromosome Location	chr1:246472491-246579373
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:648)
CpG islands
(count:123)
Chromatin interactive
region (count:34)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:648 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:246472537-246472962	K562	blood:	n/a	n/a
2	ARID3A	chr1:246476713-246476913	K562	blood:	n/a	n/a
3	ARID3A	chr1:246514223-246514241	K562	blood:	n/a	n/a
4	ARID3A	chr1:246495436-246495765	K562	blood:	n/a	n/a
5	ARID3A	chr1:246536567-246536576	K562	blood:	n/a	n/a
6	ATF1	chr1:246495450-246495686	K562	blood:	n/a	n/a
7	ATF1	chr1:246561390-246561724	K562	blood:	n/a	n/a
8	ATF1	chr1:246507966-246508030	K562	blood:	n/a	n/a
9	ATF1	chr1:246501515-246501774	K562	blood:	n/a	n/a
10	ATF1	chr1:246514087-246514345	K562	blood:	n/a	n/a
11	ATF2	chr1:246493100-246493631	GM12878	blood:	n/a	n/a
12	ATF2	chr1:246501723-246502313	GM12878	blood:	n/a	n/a
13	ATF2	chr1:246492949-246493723	GM12878	blood:	n/a	n/a
14	BACH1	chr1:246537445-246537545	K562	blood:	n/a	n/a
15	BATF	chr1:246493105-246493597	GM12878	blood:	n/a	chr1:246493346-246493357
16	BATF	chr1:246493051-246493632	GM12878	blood:	n/a	chr1:246493346-246493357
17	BATF	chr1:246501825-246502142	GM12878	blood:	n/a	n/a
18	BCL11A	chr1:246493003-246493636	GM12878	blood:	n/a	chr1:246493592-246493599 chr1:246493349-246493358
19	BCL11A	chr1:246493088-246493638	GM12878	blood:	n/a	chr1:246493592-246493599 chr1:246493349-246493358
20	BCL3	chr1:246500317-246500521	GM12878	blood:	n/a	n/a
21	BCL3	chr1:246493055-246493585	GM12878	blood:	n/a	chr1:246493349-246493358
22	BCL3	chr1:246474759-246475054	GM12878	blood:	n/a	n/a
23	BCLAF1	chr1:246493000-246493668	GM12878	blood:	n/a	chr1:246493592-246493599 chr1:246493349-246493358
24	BCLAF1	chr1:246493053-246493656	GM12878	blood:	n/a	chr1:246493592-246493599 chr1:246493349-246493358
25	BHLHE40	chr1:246506768-246506903	GM12878	blood:	n/a	n/a
26	BHLHE40	chr1:246501857-246502115	GM12878	blood:	n/a	n/a
27	BHLHE40	chr1:246493081-246493626	GM12878	blood:	n/a	n/a
28	BHLHE40	chr1:246495569-246495766	K562	blood:	n/a	n/a
29	BHLHE40	chr1:246501485-246501808	K562	blood:	n/a	n/a
30	CBX3	chr1:246554150-246554566	K562	blood:	n/a	n/a
31	CBX3	chr1:246576729-246577165	K562	blood:	n/a	n/a
32	CBX3	chr1:246554183-246554524	K562	blood:	n/a	n/a
33	CCNT2	chr1:246472666-246473033	K562	blood:	n/a	n/a
34	CCNT2	chr1:246495455-246495669	K562	blood:	n/a	n/a
35	CCNT2	chr1:246514072-246514334	K562	blood:	n/a	n/a
36	CEBPB	chr1:246488024-246488342	IMR90	lung:	n/a	n/a
37	CEBPB	chr1:246488055-246488337	A549	lung:	n/a	n/a
38	CEBPB	chr1:246559678-246559985	IMR90	lung:	n/a	chr1:246559829-246559842 chr1:246559829-246559842 chr1:246559830-246559841
39	CEBPB	chr1:246567585-246567742	K562	blood:	n/a	n/a
40	CEBPB	chr1:246559718-246559917	A549	lung:	n/a	chr1:246559829-246559842 chr1:246559829-246559842 chr1:246559830-246559841
41	CEBPB	chr1:246559741-246559980	HepG2	liver:	n/a	chr1:246559829-246559842 chr1:246559829-246559842 chr1:246559830-246559841
42	CEBPB	chr1:246487962-246488318	A549	lung:	n/a	n/a
43	CEBPB	chr1:246483583-246483947	IMR90	lung:	n/a	chr1:246483758-246483769 chr1:246483760-246483769
44	CEBPB	chr1:246487659-246487768	H1-hESC	embryonic stem cell:	n/a	n/a
45	CEBPB	chr1:246483696-246483900	HepG2	liver:	n/a	chr1:246483758-246483769 chr1:246483760-246483769
46	CEBPB	chr1:246493011-246493799	GM12878	blood:	n/a	n/a
47	CEBPB	chr1:246530442-246530743	IMR90	lung:	n/a	n/a
48	CEBPB	chr1:246483598-246483908	K562	blood:	n/a	chr1:246483758-246483769 chr1:246483760-246483769
49	CEBPB	chr1:246474391-246474534	K562	blood:	n/a	n/a
50	CEBPB	chr1:246567569-246567749	HepG2	liver:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:246518671-246518721	BJ	skin:	n/a
2	chr1:246518671-246518721	BJ	skin:	n/a
3	chr1:246518620-246518670	Hepatocyte	liver:	n/a
4	chr1:246518620-246518670	Jurkat	blood:	n/a
5	chr1:246518671-246518721	SAEC	small airway:	n/a
6	chr1:246518671-246518721	HL-60	blood:	n/a
7	chr1:246518620-246518670	LNCaP	prostate:	n/a
8	chr1:246518671-246518721	ovcar-3	ovarian:	n/a
9	chr1:246518620-246518670	AG09309	skin:	n/a
10	chr1:246518620-246518670	ovcar-3	ovarian:	n/a
11	chr1:246518671-246518721	H1-hESC	embryonic stem cell:	embryo
12	chr1:246518671-246518721	NH-A	brain:	n/a
13	chr1:246518671-246518721	HAEpiC	amniotic membrane:	n/a
14	chr1:246518671-246518721	BE2_C	brain:	n/a
15	chr1:246518671-246518721	MCF10A-Er-Src	breast:	n/a
16	chr1:246518671-246518721	PFSK-1	brain:	n/a
17	chr1:246518620-246518670	MCF-7	breast:	n/a
18	chr1:246518620-246518670	AG09319	gingival:	n/a
19	chr1:246518671-246518721	GM12891	blood:	n/a
20	chr1:246518620-246518670	HCF	heart:	n/a
21	chr1:246518671-246518721	HNPCEpiC	eye:	n/a
22	chr1:246518671-246518721	NHBE	bronchial:	n/a
23	chr1:246518671-246518721	HepG2	liver:	n/a
24	chr1:246518671-246518721	PrEC	prostate:	n/a
25	chr1:246518620-246518670	SKMC	muscle:	n/a
26	chr1:246518671-246518721	HRE	kidney:	n/a
27	chr1:246518620-246518670	HCPEpiC	choroid plexus:	n/a
28	chr1:246518671-246518721	AG04450	lung:	fetal
29	chr1:246518620-246518670	HL-60	blood:	n/a
30	chr1:246518620-246518670	RPTEC	kidney:	n/a
31	chr1:246518620-246518670	NT2-D1	testis:	n/a
32	chr1:246518671-246518721	Caco-2	colon:	n/a
33	chr1:246518671-246518721	SK-N-MC	brain:	n/a
34	chr1:246518671-246518721	SK-N-SH	brain:	n/a
35	chr1:246518671-246518721	ProgFib	skin:	n/a
36	chr1:246518671-246518721	LNCaP	prostate:	n/a
37	chr1:246518671-246518721	HCF	heart:	n/a
38	chr1:246518620-246518670	GM12892	blood:	n/a
39	chr1:246518620-246518670	ECC-1	luminal epithelium:	n/a
40	chr1:246518620-246518670	NHBE	bronchial:	n/a
41	chr1:246518671-246518721	K562	blood:	n/a
42	chr1:246518620-246518670	T-47D	breast:	n/a
43	chr1:246518620-246518670	HIPEpiC	eye:	n/a
44	chr1:246518620-246518670	IMR90	lung:	fetal
45	chr1:246518671-246518721	Hepatocyte	liver:	n/a
46	chr1:246518620-246518670	HCM	heart:	n/a
47	chr1:246518620-246518670	NH-A	brain:	n/a
48	chr1:246518620-246518670	AoSMC	blood vessel:	n/a
49	chr1:246518620-246518670	GM12891	blood:	n/a
50	chr1:246518671-246518721	IMR90	lung:	fetal

(count:34 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:246513912..246515911-chr1:246530351..246532425,2	K562	blood:
2	chr1:246576999..246579498-chr1:246580594..246582855,2	K562	blood:
3	chr1:246544799..246546719-chr1:246549229..246551594,2	K562	blood:
4	chr1:246471340..246473899-chr1:246474297..246475919,2	K562	blood:
5	chr1:246478448..246480701-chr1:246489976..246492079,2	MCF-7	breast:
6	chr1:246482242..246483844-chr1:246486769..246488361,2	MCF-7	breast:
7	chr1:246521302..246522820-chr1:246527857..246530408,2	K562	blood:
8	chr1:246489256..246490981-chr1:246569694..246571729,2	K562	blood:
9	chr1:246477291..246479573-chr1:246484385..246486637,2	K562	blood:
10	chr1:246521302..246522820-chr1:246527857..246530408,2	K562	blood:
11	chr1:246482242..246483844-chr1:246486769..246488361,2	MCF-7	breast:
12	chr1:246546236..246548052-chr1:246554234..246556624,2	MCF-7	breast:
13	chr1:246548799..246550495-chr1:246559308..246561111,2	K562	blood:
14	chr1:246513035..246514840-chr1:246515014..246517355,2	K562	blood:
15	chr1:246489256..246490981-chr1:246569694..246571729,2	K562	blood:
16	chr1:246536157..246539066-chr1:246540727..246542818,2	K562	blood:
17	chr1:246513912..246515911-chr1:246530351..246532425,2	K562	blood:
18	chr1:246480625..246484494-chr1:246484509..246487913,3	K562	blood:
19	chr1:246471340..246473899-chr1:246474297..246475919,2	K562	blood:
20	chr1:246544799..246546719-chr1:246549229..246551594,2	K562	blood:
21	chr1:246548799..246550495-chr1:246559308..246561111,2	K562	blood:
22	chr1:246540059..246542497-chr1:246543085..246545736,2	K562	blood:
23	chr1:246553361..246555954-chr1:246559201..246561583,2	K562	blood:
24	chr1:246478448..246480701-chr1:246489976..246492079,2	MCF-7	breast:
25	chr1:246546236..246548052-chr1:246554234..246556624,2	MCF-7	breast:
26	chr1:246513035..246514840-chr1:246515014..246517355,2	K562	blood:
27	chr1:246540059..246542497-chr1:246543085..246545736,2	K562	blood:
28	chr1:246463275..246466123-chr1:246471236..246474164,2	MCF-7	breast:
29	chr1:246497788..246499304-chr1:246499416..246501844,2	MCF-7	breast:
30	chr1:246057307..246059352-chr1:246513090..246515764,2	K562	blood:
31	chr1:246536157..246539066-chr1:246540727..246542818,2	K562	blood:
32	chr1:246482654..246484211-chr1:246484942..246487391,2	MCF-7	breast:
33	chr1:246553361..246555954-chr1:246559201..246561583,2	K562	blood:
34	chr1:246497788..246499304-chr1:246499416..246501844,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TFB2M-2	chr1:246484965-246485170	ENSG00000230184.1
2	lnc-TFB2M-2	chr1:246485586-246485740	ENSG00000230184.1

No data

Variant related genes	Relation type
SMYD3	TF binding region
SMYD3-IT1	TF binding region
SMYD3	CpG island
SMYD3-IT1	CpG island
ENSG00000185420	chromatin interactions
ENSG00000230184	chromatin interactions

Extended variants
information (count: 4131 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:4131 , 50 per page) page: 1 2 3 4 5 6 7 ... 83

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs568507780	chr1:246472592-246472593	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs34922799	chr1:246472644-246472645	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs534278831	chr1:246472665-246472666	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs547311440	chr1:246472668-246472669	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs570638756	chr1:246472669-246472670	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs539612603	chr1:246472676-246472677	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs375068639	chr1:246472699-246472700	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs7533584	chr1:246472732-246472733	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs572838114	chr1:246472805-246472806	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs111627323	chr1:246472831-246472832	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs143810607	chr1:246472837-246472838	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs535491321	chr1:246472865-246472866	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs185475157	chr1:246472891-246472892	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs190868114	chr1:246472941-246472942	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs527722611	chr1:246472958-246472959	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs148144535	chr1:246472973-246472974	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs115545272	chr1:246473033-246473034	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs545066404	chr1:246473113-246473114	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs182637023	chr1:246473139-246473140	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs141931259	chr1:246473149-246473150	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs114501973	chr1:246473155-246473156	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs144680380	chr1:246473163-246473164	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs552253426	chr1:246473167-246473168	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs187263981	chr1:246473191-246473192	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs562097058	chr1:246473238-246473239	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs76556712	chr1:246473284-246473285	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs537612851	chr1:246473288-246473289	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs76400493	chr1:246473289-246473290	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs527651420	chr1:246473305-246473306	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs547888550	chr1:246473331-246473332	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs191894623	chr1:246473404-246473405	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs199583406	chr1:246473488-246473489	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs386641712	chr1:246473489-246473490	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs539651693	chr1:246473492-246473493	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs549989799	chr1:246473511-246473512	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs562597177	chr1:246473539-246473540	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs569995121	chr1:246473543-246473544	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs535733951	chr1:246473659-246473660	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs571027022	chr1:246473661-246473662	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs138562065	chr1:246473689-246473690	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs141628375	chr1:246473716-246473717	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs371776824	chr1:246473810-246473811	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs376193136	chr1:246473855-246473856	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs12568702	chr1:246473902-246473903	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs183521653	chr1:246473942-246473943	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs147547229	chr1:246473963-246473964	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs386370347	chr1:246473964-246473965	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs12729175	chr1:246473978-246473979	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs12729176	chr1:246473985-246473986	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs386370348	chr1:246473986-246473987	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:87)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Melanoma	18172304	CNVD
Rett syndrome	21593744	CNVD
Medulloblastoma	21979893	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	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
Liposarcoma	21253554	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
Neuroblastoma	21899760	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Acute myeloid leukemia	20729466	CNVD
Testicular germ cell tumor	18059402	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Breast cancer	21509527	CNVD
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Hepatocellular carcinoma	18803288	CNVD
Urothelial tumor	18831757	CNVD
Lung cancer	18438408	CNVD
Medulloblastoma	16783165	CNVD
Basal cell lymphoma	17170743	CNVD
Basal cell lymphoma	17053054	CNVD
Congenital abnormalities	21549014	CNVD
Developmental delay	21549014	CNVD
Mental retardation	21549014	CNVD
small cell lung cancer	20016488	CNVD
Cancer	20164920	CNVD
Cancer	17060936	CNVD
abnormal development	18461090	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Non-small cell lung cancer	21829676	CNVD
Multiple myeloma	16616336	CNVD
Ovarian cancer	21720365	CNVD
Glioblastoma multiforme	22291905	CNVD
Myelofibrosis	22110671	CNVD
Disease	21936942	CNVD
laryngomalacia	21936942	CNVD
GLUT3 deficiency syndrome	20509907	CNVD
Developmental delay	21373258	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Developmental delay	19490664	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Cutaneous malignant melanoma	18794153	CNVD
Astrocytoma	17934521	CNVD
Neurocytoma	17123091	CNVD
Central neurocytomas	17123091	CNVD
Breast cancer	20409316	CNVD
Fibroblasts	17951408	CNVD
Lung cancer	17951408	CNVD
Schizophrenia	20967226	CNVD
Bipolar disorder	19114987	CNVD
Schizophrenia	19805367	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:572 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:246423400-246509000	Weak transcription	Aorta	Aorta
2	chr1:246441800-246506600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
3	chr1:246447600-246482400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr1:246447600-246502800	Weak transcription	Left Ventricle	heart
5	chr1:246455000-246493000	Weak transcription	Primary B cells from cord blood	blood
6	chr1:246461800-246493000	Weak transcription	Primary T cells from cord blood	blood
7	chr1:246465600-246480800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
8	chr1:246465600-246518800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr1:246465800-246486600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr1:246466200-246480600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
11	chr1:246466600-246480600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
12	chr1:246468600-246482400	Weak transcription	Fetal Kidney	kidney
13	chr1:246470400-246493000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
14	chr1:246471400-246473600	Weak transcription	K562	blood
15	chr1:246472000-246474000	Enhancers	Primary hematopoietic stem cells short term culture	blood
16	chr1:246472200-246473400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr1:246472400-246473200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
18	chr1:246472400-246475800	Weak transcription	Osteobl	bone
19	chr1:246473200-246482600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
20	chr1:246473400-246482400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr1:246473400-246519200	Weak transcription	Pancreas	Pancrea
22	chr1:246473600-246473800	Enhancers	K562	blood
23	chr1:246474000-246477800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
24	chr1:246474600-246504800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr1:246475000-246475200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
26	chr1:246475200-246475400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr1:246475200-246475400	Enhancers	Spleen	Spleen
28	chr1:246475200-246475600	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr1:246475800-246476000	Enhancers	Esophagus	oesophagus
30	chr1:246475800-246476200	Strong transcription	Osteobl	bone
31	chr1:246476200-246480800	Weak transcription	Osteobl	bone
32	chr1:246477800-246478600	Enhancers	Primary hematopoietic stem cells short term culture	blood
33	chr1:246478600-246482400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
34	chr1:246480400-246480800	Enhancers	iPS-20b Cell Line	embryonic stem cell
35	chr1:246480400-246481000	Enhancers	ES-I3 Cell Line	embryonic stem cell
36	chr1:246480400-246481000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
37	chr1:246480400-246481000	Enhancers	HUES48 Cell Line	embryonic stem cell
38	chr1:246480400-246481200	Enhancers	HUES64 Cell Line	embryonic stem cell
39	chr1:246480600-246481000	Enhancers	H9 Cell Line	embryonic stem cell
40	chr1:246480600-246481000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr1:246480600-246481000	Enhancers	HUES6 Cell Line	embryonic stem cell
42	chr1:246480600-246481000	Enhancers	iPS-15b Cell Line	embryonic stem cell
43	chr1:246480600-246481000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
44	chr1:246480600-246481000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
45	chr1:246480600-246481000	Enhancers	Fetal Brain Female	brain
46	chr1:246480600-246481400	Enhancers	HSMM	muscle
47	chr1:246480600-246481600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
48	chr1:246480600-246482000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
49	chr1:246480600-246482200	Enhancers	NHDF-Ad	bronchial
50	chr1:246480600-246482600	Enhancers	Muscle Satellite Cultured Cells	--

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