Variant report

Variant	nsv1006486
Chromosome Location	chr1:246249325-246274576
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:216)
CpG islands
(count:183)
Chromatin interactive
region (count:24)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:216 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:246268344-246268607	K562	blood:	n/a	n/a
2	ARID3A	chr1:246273822-246274255	K562	blood:	n/a	n/a
3	ARID3A	chr1:246254962-246255161	K562	blood:	n/a	n/a
4	ARID3A	chr1:246269535-246270147	K562	blood:	n/a	n/a
5	ATF1	chr1:246254868-246255152	K562	blood:	n/a	n/a
6	ATF1	chr1:246269670-246270067	K562	blood:	n/a	n/a
7	ATF1	chr1:246273843-246274253	K562	blood:	n/a	n/a
8	ATF1	chr1:246271408-246271755	K562	blood:	n/a	n/a
9	ATF3	chr1:246268210-246268637	K562	blood:	n/a	n/a
10	BACH1	chr1:246273993-246274130	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr1:246273777-246274254	K562	blood:	n/a	n/a
12	BHLHE40	chr1:246268352-246268551	K562	blood:	n/a	n/a
13	BHLHE40	chr1:246273673-246274211	K562	blood:	n/a	n/a
14	BHLHE40	chr1:246258872-246259140	K562	blood:	n/a	n/a
15	BHLHE40	chr1:246272061-246272063	K562	blood:	n/a	n/a
16	BHLHE40	chr1:246269858-246269979	K562	blood:	n/a	n/a
17	CBX3	chr1:246273628-246274320	K562	blood:	n/a	n/a
18	CCNT2	chr1:246269695-246270115	K562	blood:	n/a	n/a
19	CCNT2	chr1:246273669-246274178	K562	blood:	n/a	n/a
20	CEBPB	chr1:246267774-246268042	HepG2	liver:	n/a	chr1:246267896-246267907
21	CEBPB	chr1:246263358-246263520	IMR90	lung:	n/a	chr1:246263463-246263474
22	CEBPB	chr1:246273930-246274272	IMR90	lung:	n/a	n/a
23	CEBPB	chr1:246273825-246274299	K562	blood:	n/a	n/a
24	CEBPB	chr1:246271311-246271649	K562	blood:	n/a	n/a
25	CEBPB	chr1:246263291-246263649	HepG2	liver:	n/a	chr1:246263463-246263474
26	CEBPB	chr1:246273847-246274169	A549	lung:	n/a	n/a
27	CEBPB	chr1:246267752-246268054	K562	blood:	n/a	chr1:246267896-246267907
28	CEBPB	chr1:246269802-246270102	K562	blood:	n/a	n/a
29	CEBPB	chr1:246263330-246263551	K562	blood:	n/a	chr1:246263463-246263474
30	CEBPB	chr1:246273880-246274363	K562	blood:	n/a	n/a
31	CEBPB	chr1:246268277-246268581	K562	blood:	n/a	n/a
32	CTCF	chr1:246251460-246251610	GM12864	blood:	n/a	n/a
33	CTCF	chr1:246268776-246268897	K562	blood:	n/a	n/a
34	CTCF	chr1:246267000-246267150	GM12868	blood:	n/a	n/a
35	CUX1	chr1:246269423-246270131	K562	blood:	n/a	n/a
36	CUX1	chr1:246268295-246268912	K562	blood:	n/a	n/a
37	E2F4	chr1:246264096-246264180	MCF10A-Er-Src	breast:	n/a	n/a
38	E2F4	chr1:246268307-246268471	MCF10A-Er-Src	breast:	n/a	n/a
39	EP300	chr1:246273836-246274117	SK-N-SH_RA	brain:	n/a	n/a
40	EP300	chr1:246269699-246270044	SK-N-SH_RA	brain:	n/a	n/a
41	EP300	chr1:246270785-246271209	SK-N-SH_RA	brain:	n/a	n/a
42	EP300	chr1:246268314-246268619	K562	blood:	n/a	n/a
43	EP300	chr1:246269692-246269942	K562	blood:	n/a	n/a
44	EP300	chr1:246269747-246270039	SK-N-SH_RA	brain:	n/a	n/a
45	EP300	chr1:246270804-246271142	SK-N-SH_RA	brain:	n/a	n/a
46	EP300	chr1:246270722-246271352	SK-N-SH	brain:	n/a	chr1:246271213-246271227
47	EP300	chr1:246269578-246270037	K562	blood:	n/a	n/a
48	EP300	chr1:246273661-246274356	K562	blood:	n/a	chr1:246274317-246274331
49	EP300	chr1:246270476-246272130	SK-N-SH	brain:	n/a	chr1:246271213-246271227 chr1:246271441-246271450 chr1:246270654-246270668 chr1:246272058-246272068
50	EP300	chr1:246254900-246255119	K562	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:246254338-246254388	NHBE	bronchial:	n/a
2	chr1:246254338-246254388	AG04450	lung:	fetal
3	chr1:246254215-246254265	NH-A	brain:	n/a
4	chr1:246254215-246254265	H1-hESC	embryonic stem cell:	embryo
5	chr1:246254283-246254333	LNCaP	prostate:	n/a
6	chr1:246254338-246254388	HNPCEpiC	eye:	n/a
7	chr1:246254338-246254388	HIPEpiC	eye:	n/a
8	chr1:246254338-246254388	HEEpiC	esophagus:	n/a
9	chr1:246254215-246254265	SAEC	small airway:	n/a
10	chr1:246254215-246254265	MCF-7	breast:	n/a
11	chr1:246254215-246254265	HEEpiC	esophagus:	n/a
12	chr1:246254283-246254333	HRCEpiC	kidney:	n/a
13	chr1:246254338-246254388	ovcar-3	ovarian:	n/a
14	chr1:246254338-246254388	GM06990	blood:	n/a
15	chr1:246254283-246254333	SAEC	small airway:	n/a
16	chr1:246254215-246254265	HUVEC	blood vessel:	n/a
17	chr1:246254283-246254333	GM19239	blood:	n/a
18	chr1:246254215-246254265	HCF	heart:	n/a
19	chr1:246254215-246254265	ECC-1	luminal epithelium:	n/a
20	chr1:246254215-246254265	NHBE	bronchial:	n/a
21	chr1:246254215-246254265	PrEC	prostate:	n/a
22	chr1:246254215-246254265	Caco-2	colon:	n/a
23	chr1:246254215-246254265	A549	lung:	n/a
24	chr1:246254283-246254333	HEK293	kidney:	embryo
25	chr1:246254283-246254333	BJ	skin:	n/a
26	chr1:246254283-246254333	ECC-1	luminal epithelium:	n/a
27	chr1:246254283-246254333	U87	brain:	n/a
28	chr1:246254215-246254265	SKMC	muscle:	n/a
29	chr1:246254338-246254388	NB4	blood:	n/a
30	chr1:246254283-246254333	IMR90	lung:	fetal
31	chr1:246254215-246254265	BE2_C	brain:	n/a
32	chr1:246254338-246254388	A549	lung:	n/a
33	chr1:246254215-246254265	NHDF-neo	bronchial:	n/a
34	chr1:246254338-246254388	HMEC	breast:	n/a
35	chr1:246254338-246254388	AG10803	skin:	n/a
36	chr1:246254338-246254388	IMR90	lung:	fetal
37	chr1:246254283-246254333	GM12878	blood:	n/a
38	chr1:246254215-246254265	CMK	blood:	n/a
39	chr1:246254338-246254388	SKMC	muscle:	n/a
40	chr1:246254283-246254333	HPAEpiC	pulmonary alveolar:	n/a
41	chr1:246254338-246254388	MCF10A-Er-Src	breast:	n/a
42	chr1:246254215-246254265	GM12892	blood:	n/a
43	chr1:246254283-246254333	RPTEC	kidney:	n/a
44	chr1:246254338-246254388	NT2-D1	testis:	n/a
45	chr1:246254215-246254265	GM12878	blood:	n/a
46	chr1:246254215-246254265	ovcar-3	ovarian:	n/a
47	chr1:246254215-246254265	T-47D	breast:	n/a
48	chr1:246254338-246254388	GM12892	blood:	n/a
49	chr1:246254215-246254265	HIPEpiC	eye:	n/a
50	chr1:246254283-246254333	T-47D	breast:	n/a

(count:24 , 50 per page) page: 1

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

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KIF26B-2	chr1:246273081-246273195	NONHSAT010700
2	lnc-KIF26B-2	chr1:246273084-246273195	ENSG00000226876.1
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
ENSG00000202184	chromatin interactions
ENSG00000226876	chromatin interactions
ENSG00000185420	chromatin interactions

Extended variants
information (count: 1160 )
Associated
traits (count: 86 )

Variant overlapped rSNPs/rCNVs (count:1160 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs555350311	chr1:246249325-246249326	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs572059630	chr1:246249338-246249339	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs73139807	chr1:246249339-246249340	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs374796947	chr1:246249359-246249360	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs564278973	chr1:246249441-246249442	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs533250613	chr1:246249472-246249473	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs543626246	chr1:246249473-246249474	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs2993470	chr1:246249475-246249476	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs79292187	chr1:246249480-246249481	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs549252373	chr1:246249487-246249488	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs565977715	chr1:246249517-246249518	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs546833670	chr1:246249534-246249535	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs184121882	chr1:246249576-246249577	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs551381792	chr1:246249577-246249578	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs571345183	chr1:246249586-246249587	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs140984098	chr1:246249593-246249594	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs371084768	chr1:246249597-246249598	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs375248318	chr1:246249601-246249602	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs556731893	chr1:246249609-246249610	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs188875115	chr1:246249626-246249627	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs2787988	chr1:246249639-246249640	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
22	rs555684838	chr1:246249657-246249658	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs118045381	chr1:246249663-246249664	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs537048703	chr1:246249672-246249673	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs541059152	chr1:246249691-246249692	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs193108884	chr1:246249694-246249695	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs578061382	chr1:246249754-246249755	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs185364741	chr1:246249941-246249942	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs59896007	chr1:246249949-246249950	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs201039814	chr1:246250005-246250006	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs377621858	chr1:246250012-246250013	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs138508758	chr1:246250014-246250015	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs112531334	chr1:246250016-246250017	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs567631672	chr1:246250030-246250031	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs188371097	chr1:246250062-246250063	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs564691542	chr1:246250064-246250065	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs530636724	chr1:246250087-246250088	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs550355091	chr1:246250100-246250101	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs567352296	chr1:246250105-246250106	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs113368613	chr1:246250109-246250110	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs141852169	chr1:246250152-246250153	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs566059483	chr1:246250256-246250257	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs534953446	chr1:246250273-246250274	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs558143220	chr1:246250290-246250291	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs146285975	chr1:246250299-246250300	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs537449560	chr1:246250362-246250363	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs557216991	chr1:246250378-246250379	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs574168744	chr1:246250392-246250393	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs112685554	chr1:246250433-246250434	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs4654192	chr1:246250449-246250450	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	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:253 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:246203800-246257600	Weak transcription	Primary T cells from cord blood	blood
2	chr1:246245800-246253000	Weak transcription	Aorta	Aorta
3	chr1:246247800-246253800	Weak transcription	Placenta	Placenta
4	chr1:246247800-246273800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr1:246248000-246252400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
6	chr1:246248800-246249800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
7	chr1:246249800-246252400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr1:246251800-246253000	Weak transcription	Primary hematopoietic stem cells	blood
9	chr1:246252400-246253600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
10	chr1:246252400-246255400	Enhancers	Primary hematopoietic stem cells short term culture	blood
11	chr1:246253000-246253200	Enhancers	Primary hematopoietic stem cells	blood
12	chr1:246253000-246253200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
13	chr1:246253000-246253200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr1:246253000-246253200	Enhancers	Aorta	Aorta
15	chr1:246253200-246254800	Weak transcription	Primary hematopoietic stem cells	blood
16	chr1:246253400-246254400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr1:246253400-246254600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
18	chr1:246253600-246254000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
19	chr1:246253800-246254600	Enhancers	Placenta	Placenta
20	chr1:246253800-246256200	Enhancers	Primary monocytes fromperipheralblood	blood
21	chr1:246254000-246255400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
22	chr1:246254200-246254800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
23	chr1:246254200-246255200	Enhancers	K562	blood
24	chr1:246254400-246254600	Enhancers	Thymus	Thymus
25	chr1:246254400-246255400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
26	chr1:246254400-246255600	Enhancers	Monocytes-CD14+_RO01746	blood
27	chr1:246254400-246256000	Enhancers	Primary neutrophils fromperipheralblood	blood
28	chr1:246254600-246255000	Enhancers	Fetal Stomach	stomach
29	chr1:246254600-246256400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
30	chr1:246254800-246256200	Enhancers	Primary hematopoietic stem cells	blood
31	chr1:246255000-246255200	Enhancers	Skeletal Muscle Male	skeletal muscle
32	chr1:246255200-246267600	Weak transcription	K562	blood
33	chr1:246255400-246255600	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
34	chr1:246255400-246256000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
35	chr1:246255400-246259200	Weak transcription	Skeletal Muscle Male	skeletal muscle
36	chr1:246255600-246255800	Enhancers	Primary hematopoietic stem cells short term culture	blood
37	chr1:246255600-246256000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
38	chr1:246255800-246256000	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
39	chr1:246256000-246256200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
40	chr1:246256000-246256400	Enhancers	Monocytes-CD14+_RO01746	blood
41	chr1:246256000-246256600	Enhancers	Primary hematopoietic stem cells short term culture	blood
42	chr1:246256600-246258200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
43	chr1:246257400-246268400	Weak transcription	Osteobl	bone
44	chr1:246257600-246258200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
45	chr1:246257600-246258400	Strong transcription	Primary T cells from cord blood	blood
46	chr1:246258000-246259200	Enhancers	Stomach Smooth Muscle	stomach
47	chr1:246258200-246258400	Genic enhancers	Primary hematopoietic stem cells short term culture	blood
48	chr1:246258200-246259000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr1:246258200-246260400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
50	chr1:246258400-246259000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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