Variant report

Variant	nsv535400
Chromosome Location	chr1:246241061-246274576
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:277)
CpG islands
(count:183)
Chromatin interactive
region (count:30)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:277 , 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	ARID3A	chr1:246269535-246270147	K562	blood:	n/a	n/a
2	ARID3A	chr1:246273822-246274255	K562	blood:	n/a	n/a
3	ARID3A	chr1:246268344-246268607	K562	blood:	n/a	n/a
4	ARID3A	chr1:246254962-246255161	K562	blood:	n/a	n/a
5	ATF1	chr1:246273843-246274253	K562	blood:	n/a	n/a
6	ATF1	chr1:246241695-246242195	K562	blood:	n/a	n/a
7	ATF1	chr1:246254868-246255152	K562	blood:	n/a	n/a
8	ATF1	chr1:246271408-246271755	K562	blood:	n/a	n/a
9	ATF1	chr1:246269670-246270067	K562	blood:	n/a	n/a
10	ATF3	chr1:246268210-246268637	K562	blood:	n/a	n/a
11	BACH1	chr1:246273993-246274130	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr1:246273777-246274254	K562	blood:	n/a	n/a
13	BHLHE40	chr1:246258872-246259140	K562	blood:	n/a	n/a
14	BHLHE40	chr1:246272061-246272063	K562	blood:	n/a	n/a
15	BHLHE40	chr1:246268352-246268551	K562	blood:	n/a	n/a
16	BHLHE40	chr1:246269858-246269979	K562	blood:	n/a	n/a
17	BHLHE40	chr1:246273673-246274211	K562	blood:	n/a	n/a
18	CBX3	chr1:246273628-246274320	K562	blood:	n/a	n/a
19	CBX3	chr1:246245179-246246286	K562	blood:	n/a	n/a
20	CBX3	chr1:246245635-246245944	K562	blood:	n/a	n/a
21	CBX3	chr1:246241614-246242251	K562	blood:	n/a	n/a
22	CCNT2	chr1:246273669-246274178	K562	blood:	n/a	n/a
23	CCNT2	chr1:246269695-246270115	K562	blood:	n/a	n/a
24	CEBPB	chr1:246268277-246268581	K562	blood:	n/a	n/a
25	CEBPB	chr1:246267752-246268054	K562	blood:	n/a	chr1:246267896-246267907
26	CEBPB	chr1:246263330-246263551	K562	blood:	n/a	chr1:246263463-246263474
27	CEBPB	chr1:246267774-246268042	HepG2	liver:	n/a	chr1:246267896-246267907
28	CEBPB	chr1:246263291-246263649	HepG2	liver:	n/a	chr1:246263463-246263474
29	CEBPB	chr1:246271311-246271649	K562	blood:	n/a	n/a
30	CEBPB	chr1:246273930-246274272	IMR90	lung:	n/a	n/a
31	CEBPB	chr1:246273880-246274363	K562	blood:	n/a	n/a
32	CEBPB	chr1:246273825-246274299	K562	blood:	n/a	n/a
33	CEBPB	chr1:246269802-246270102	K562	blood:	n/a	n/a
34	CEBPB	chr1:246273847-246274169	A549	lung:	n/a	n/a
35	CEBPB	chr1:246263358-246263520	IMR90	lung:	n/a	chr1:246263463-246263474
36	CTCF	chr1:246251460-246251610	GM12864	blood:	n/a	n/a
37	CTCF	chr1:246267000-246267150	GM12868	blood:	n/a	n/a
38	CTCF	chr1:246243678-246243706	GM10248	blood:	n/a	n/a
39	CTCF	chr1:246241040-246241190	WI-38	lung:	n/a	n/a
40	CTCF	chr1:246243774-246243857	Lung_OC	lung:	n/a	n/a
41	CTCF	chr1:246246953-246246971	GM10248	blood:	n/a	n/a
42	CTCF	chr1:246268776-246268897	K562	blood:	n/a	n/a
43	CUX1	chr1:246269423-246270131	K562	blood:	n/a	n/a
44	CUX1	chr1:246268295-246268912	K562	blood:	n/a	n/a
45	CUX1	chr1:246241510-246242267	K562	blood:	n/a	n/a
46	E2F4	chr1:246264096-246264180	MCF10A-Er-Src	breast:	n/a	n/a
47	E2F4	chr1:246268307-246268471	MCF10A-Er-Src	breast:	n/a	n/a
48	EP300	chr1:246273661-246274356	K562	blood:	n/a	chr1:246274317-246274331
49	EP300	chr1:246270722-246271352	SK-N-SH	brain:	n/a	chr1:246271213-246271227
50	EP300	chr1:246269699-246270044	SK-N-SH_RA	brain:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:246254215-246254265	Hepatocyte	liver:	n/a
2	chr1:246254215-246254265	HCF	heart:	n/a
3	chr1:246254215-246254265	HRPEpiC	eye:	n/a
4	chr1:246254283-246254333	SK-N-SH_RA	brain:	n/a
5	chr1:246254338-246254388	GM19239	blood:	n/a
6	chr1:246254215-246254265	AG10803	skin:	n/a
7	chr1:246254283-246254333	GM19239	blood:	n/a
8	chr1:246254338-246254388	HIPEpiC	eye:	n/a
9	chr1:246254215-246254265	NH-A	brain:	n/a
10	chr1:246254215-246254265	HUVEC	blood vessel:	n/a
11	chr1:246254338-246254388	Caco-2	colon:	n/a
12	chr1:246254338-246254388	HCM	heart:	n/a
13	chr1:246254338-246254388	SAEC	small airway:	n/a
14	chr1:246254215-246254265	ECC-1	luminal epithelium:	n/a
15	chr1:246254283-246254333	K562	blood:	n/a
16	chr1:246254338-246254388	SK-N-SH_RA	brain:	n/a
17	chr1:246254283-246254333	HCM	heart:	n/a
18	chr1:246254338-246254388	ProgFib	skin:	n/a
19	chr1:246254283-246254333	NT2-D1	testis:	n/a
20	chr1:246254283-246254333	BE2_C	brain:	n/a
21	chr1:246254283-246254333	SK-N-SH	brain:	n/a
22	chr1:246254215-246254265	BJ	skin:	n/a
23	chr1:246254338-246254388	AG10803	skin:	n/a
24	chr1:246254338-246254388	HCF	heart:	n/a
25	chr1:246254283-246254333	HRCEpiC	kidney:	n/a
26	chr1:246254215-246254265	HRCEpiC	kidney:	n/a
27	chr1:246254283-246254333	AG09319	gingival:	n/a
28	chr1:246254283-246254333	PANC-1	pancreas:	n/a
29	chr1:246254215-246254265	HCM	heart:	n/a
30	chr1:246254338-246254388	HEEpiC	esophagus:	n/a
31	chr1:246254283-246254333	T-47D	breast:	n/a
32	chr1:246254338-246254388	H1-hESC	embryonic stem cell:	embryo
33	chr1:246254338-246254388	BJ	skin:	n/a
34	chr1:246254215-246254265	HepG2	liver:	n/a
35	chr1:246254338-246254388	A549	lung:	n/a
36	chr1:246254215-246254265	LNCaP	prostate:	n/a
37	chr1:246254338-246254388	NHBE	bronchial:	n/a
38	chr1:246254338-246254388	BE2_C	brain:	n/a
39	chr1:246254283-246254333	AG04450	lung:	fetal
40	chr1:246254215-246254265	SK-N-SH_RA	brain:	n/a
41	chr1:246254215-246254265	Jurkat	blood:	n/a
42	chr1:246254215-246254265	MCF-7	breast:	n/a
43	chr1:246254283-246254333	SK-N-MC	brain:	n/a
44	chr1:246254283-246254333	HCF	heart:	n/a
45	chr1:246254215-246254265	NHBE	bronchial:	n/a
46	chr1:246254283-246254333	HepG2	liver:	n/a
47	chr1:246254215-246254265	H1-hESC	embryonic stem cell:	embryo
48	chr1:246254283-246254333	HAEpiC	amniotic membrane:	n/a
49	chr1:246254215-246254265	HRE	kidney:	n/a
50	chr1:246254338-246254388	SK-N-SH	brain:	n/a

(count:30 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:246268677..246271213-chr1:246273577..246275515,2	MCF-7	breast:
2	chr1:246242761..246244330-chr1:246271984..246274792,2	K562	blood:
3	chr1:246259009..246261177-chr1:246350968..246353474,2	K562	blood:
4	chr1:246244386..246246974-chr1:246250751..246252687,2	K562	blood:
5	chr1:246262654..246264469-chr1:246272321..246273994,2	K562	blood:
6	chr1:246235580..246237637-chr1:246239913..246241714,2	K562	blood:
7	chr1:246267866..246270961-chr1:246274168..246280480,6	K562	blood:
8	chr1:246268548..246271148-chr1:246275911..246279561,4	K562	blood:
9	chr1:246261803..246263776-chr1:246265418..246268035,2	K562	blood:
10	chr1:246242761..246244330-chr1:246271984..246274792,2	K562	blood:
11	chr1:246265696..246267807-chr1:246269289..246271146,2	MCF-7	breast:
12	chr1:246260025..246262798-chr1:246267872..246269623,2	K562	blood:
13	chr1:246265696..246267807-chr1:246269289..246271146,2	MCF-7	breast:
14	chr1:246273236..246275581-chr1:246292847..246295788,2	K562	blood:
15	chr1:246240012..246241655-chr1:246242133..246245121,2	K562	blood:
16	chr1:246268677..246271213-chr1:246273577..246275515,2	MCF-7	breast:
17	chr1:246267010..246267515-chr5:115973253..115974226,2	MCF-7	breast:
18	chr1:246261134..246264107-chr1:246270558..246273069,4	K562	blood:
19	chr1:246250496..246253132-chr1:246262575..246264786,2	K562	blood:
20	chr1:246240012..246241655-chr1:246242133..246245121,2	K562	blood:
21	chr1:246237075..246239017-chr1:246241942..246243808,2	K562	blood:
22	chr1:246262654..246264469-chr1:246272321..246273994,2	K562	blood:
23	chr1:246260025..246262798-chr1:246267872..246269623,2	K562	blood:
24	chr1:246272101..246273950-chr1:246817056..246818596,2	K562	blood:
25	chr1:246254942..246257764-chr1:246259415..246261658,2	K562	blood:
26	chr1:246244386..246246974-chr1:246250751..246252687,2	K562	blood:
27	chr1:246261803..246263776-chr1:246265418..246268035,2	K562	blood:
28	chr1:246250496..246253132-chr1:246262575..246264786,2	K562	blood:
29	chr1:246267866..246270961-chr1:246274168..246280480,6	K562	blood:
30	chr1:246254942..246257764-chr1:246259415..246261815,3	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KIF26B-2	chr1:246273084-246273195	ENSG00000226876.1
2	lnc-KIF26B-2	chr1:246273081-246273195	NONHSAT010700
3	lnc-KIF26B-2	chr1:246271928-246272019	ENSG00000226876.1

No data

Variant related genes	Relation type
ENSG00000226876	TF binding region
SMYD3	TF binding region
ENSG00000226876	CpG island
SMYD3	CpG island
ENSG00000226876	chromatin interactions
ENSG00000202184	chromatin interactions
ENSG00000185420	chromatin interactions

Extended variants
information (count: 1551 )
Associated
traits (count: 86 )

Variant overlapped rSNPs/rCNVs (count:1551 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs77226390	chr1:246241085-246241086	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs147346282	chr1:246241102-246241103	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs368091494	chr1:246241103-246241104	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs557123734	chr1:246241118-246241119	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs148487271	chr1:246241129-246241130	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs541438863	chr1:246241150-246241151	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs180829509	chr1:246241157-246241158	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs536572467	chr1:246241169-246241170	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs529064342	chr1:246241181-246241182	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs142650344	chr1:246241196-246241197	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs112831447	chr1:246241227-246241228	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs77363362	chr1:246241320-246241321	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs28642395	chr1:246241406-246241407	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs544456571	chr1:246241464-246241465	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs150984989	chr1:246241470-246241471	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs530025744	chr1:246241471-246241472	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs2788012	chr1:246241489-246241490	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs140854916	chr1:246241523-246241524	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs186130841	chr1:246241532-246241533	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs61839075	chr1:246241574-246241575	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs143367131	chr1:246241578-246241579	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs146588399	chr1:246241585-246241586	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs550789906	chr1:246241586-246241587	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs75565404	chr1:246241643-246241644	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs536966355	chr1:246241663-246241664	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs546934998	chr1:246241700-246241701	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs141288236	chr1:246241716-246241717	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs145011814	chr1:246241759-246241760	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs551692489	chr1:246241792-246241793	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs558980057	chr1:246241809-246241810	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs367791617	chr1:246241846-246241847	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs2788013	chr1:246241892-246241893	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs538316061	chr1:246241921-246241922	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs191808661	chr1:246241949-246241950	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs12039063	chr1:246241962-246241963	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs540524659	chr1:246241987-246241988	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs550967015	chr1:246241988-246241989	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs183369103	chr1:246242016-246242017	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs116741451	chr1:246242043-246242044	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs2787961	chr1:246242044-246242045	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs562121120	chr1:246242107-246242108	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs113982533	chr1:246242143-246242144	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs374847327	chr1:246242178-246242179	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs187880013	chr1:246242193-246242194	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs2787960	chr1:246242240-246242241	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
46	rs71638312	chr1:246242274-246242275	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs10924493	chr1:246242275-246242276	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs138689693	chr1:246242294-246242295	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs114287915	chr1:246242312-246242313	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs539320929	chr1:246242387-246242388	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:86)

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
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:308 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:246203800-246257600	Weak transcription	Primary T cells from cord blood	blood
2	chr1:246235800-246244600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
3	chr1:246235800-246245600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr1:246238800-246242400	Enhancers	Primary hematopoietic stem cells short term culture	blood
5	chr1:246240600-246243400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr1:246240800-246241400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr1:246240800-246241800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
8	chr1:246240800-246241800	Weak transcription	Ovary	ovary
9	chr1:246241000-246241200	Flanking Active TSS	K562	blood
10	chr1:246241000-246242600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr1:246241000-246242800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
12	chr1:246241200-246241400	Enhancers	K562	blood
13	chr1:246241400-246242000	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr1:246241400-246242200	Flanking Active TSS	K562	blood
15	chr1:246241400-246245600	Enhancers	HepG2	liver
16	chr1:246241800-246242000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
17	chr1:246241800-246242600	Enhancers	Ovary	ovary
18	chr1:246242000-246242600	Enhancers	Primary hematopoietic stem cells	blood
19	chr1:246242000-246242600	Enhancers	Primary T regulatory cells fromperipheralblood	blood
20	chr1:246242200-246242600	Enhancers	K562	blood
21	chr1:246242400-246244400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
22	chr1:246242600-246243400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
23	chr1:246242600-246244000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
24	chr1:246242600-246245200	Weak transcription	Primary hematopoietic stem cells	blood
25	chr1:246243400-246244200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
26	chr1:246244000-246245600	Enhancers	Primary T regulatory cells fromperipheralblood	blood
27	chr1:246244200-246244400	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
28	chr1:246244200-246245000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
29	chr1:246244200-246245200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
30	chr1:246244400-246245200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
31	chr1:246244400-246245600	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
32	chr1:246244600-246246000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
33	chr1:246244600-246246600	Enhancers	Placenta	Placenta
34	chr1:246244800-246245600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
35	chr1:246244800-246245600	Enhancers	Fetal Thymus	thymus
36	chr1:246245000-246245400	Weak transcription	HUES64 Cell Line	embryonic stem cell
37	chr1:246245200-246245400	ZNF genes & repeats	Primary hematopoietic stem cells	blood
38	chr1:246245200-246246000	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
39	chr1:246245200-246246000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
40	chr1:246245200-246246000	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
41	chr1:246245600-246245800	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
42	chr1:246245600-246245800	ZNF genes & repeats	Aorta	Aorta
43	chr1:246245600-246246000	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
44	chr1:246245600-246246000	ZNF genes & repeats	Lung	lung
45	chr1:246245800-246253000	Weak transcription	Aorta	Aorta
46	chr1:246246000-246246600	Weak transcription	Lung	lung
47	chr1:246246000-246247400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
48	chr1:246246000-246247600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
49	chr1:246246600-246246800	Active TSS	Placenta	Placenta
50	chr1:246246800-246247000	Enhancers	Fetal Intestine Large	intestine

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