Variant report

Variant	nsv999902
Chromosome Location	chr1:246530451-246608224
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:498)
CpG islands
(count:427)
Chromatin interactive
region (count:26)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:498 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:246587912-246588291	K562	blood:	n/a	n/a
2	ARID3A	chr1:246536567-246536576	K562	blood:	n/a	n/a
3	ARID3A	chr1:246591789-246592119	K562	blood:	n/a	n/a
4	ATF1	chr1:246589653-246589853	K562	blood:	n/a	n/a
5	ATF1	chr1:246591887-246592268	K562	blood:	n/a	n/a
6	ATF1	chr1:246588435-246588914	K562	blood:	n/a	n/a
7	ATF1	chr1:246561390-246561724	K562	blood:	n/a	n/a
8	ATF2	chr1:246598868-246599249	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr1:246537445-246537545	K562	blood:	n/a	n/a
10	BACH1	chr1:246606450-246606451	K562	blood:	n/a	n/a
11	BACH1	chr1:246591894-246592194	K562	blood:	n/a	n/a
12	BATF	chr1:246591880-246592213	GM12878	blood:	n/a	n/a
13	BATF	chr1:246591816-246592158	GM12878	blood:	n/a	n/a
14	BCL11A	chr1:246591893-246592220	GM12878	blood:	n/a	n/a
15	BCL11A	chr1:246591909-246592164	GM12878	blood:	n/a	n/a
16	BHLHE40	chr1:246591822-246592280	K562	blood:	n/a	n/a
17	BHLHE40	chr1:246580932-246580933	K562	blood:	n/a	n/a
18	BHLHE40	chr1:246588462-246588796	K562	blood:	n/a	n/a
19	BRCA1	chr1:246598938-246599254	H1-hESC	embryonic stem cell:	n/a	n/a
20	CBX3	chr1:246591794-246592269	K562	blood:	n/a	n/a
21	CBX3	chr1:246554183-246554524	K562	blood:	n/a	n/a
22	CBX3	chr1:246582052-246582537	K562	blood:	n/a	n/a
23	CBX3	chr1:246591771-246592290	K562	blood:	n/a	n/a
24	CBX3	chr1:246588426-246589002	K562	blood:	n/a	n/a
25	CBX3	chr1:246580386-246580871	K562	blood:	n/a	n/a
26	CBX3	chr1:246576729-246577165	K562	blood:	n/a	n/a
27	CBX3	chr1:246554150-246554566	K562	blood:	n/a	n/a
28	CBX3	chr1:246581941-246582555	K562	blood:	n/a	n/a
29	CCNT2	chr1:246588441-246589002	K562	blood:	n/a	n/a
30	CEBPB	chr1:246559678-246559985	IMR90	lung:	n/a	chr1:246559829-246559842 chr1:246559829-246559842 chr1:246559830-246559841
31	CEBPB	chr1:246598435-246599408	H1-hESC	embryonic stem cell:	n/a	chr1:246598811-246598823 chr1:246598665-246598678
32	CEBPB	chr1:246591783-246592270	K562	blood:	n/a	n/a
33	CEBPB	chr1:246598407-246599012	IMR90	lung:	n/a	chr1:246598811-246598823 chr1:246598665-246598678
34	CEBPB	chr1:246588404-246588847	K562	blood:	n/a	n/a
35	CEBPB	chr1:246598491-246599425	Hela-S3	cervix:	n/a	chr1:246598811-246598823 chr1:246598665-246598678
36	CEBPB	chr1:246598418-246598737	HepG2	liver:	n/a	chr1:246598665-246598678
37	CEBPB	chr1:246567585-246567742	K562	blood:	n/a	n/a
38	CEBPB	chr1:246598407-246598920	K562	blood:	n/a	chr1:246598811-246598823 chr1:246598665-246598678
39	CEBPB	chr1:246559669-246559992	K562	blood:	n/a	chr1:246559829-246559842 chr1:246559829-246559842 chr1:246559830-246559841
40	CEBPB	chr1:246567569-246567749	HepG2	liver:	n/a	n/a
41	CEBPB	chr1:246598404-246598904	A549	lung:	n/a	chr1:246598811-246598823 chr1:246598665-246598678
42	CEBPB	chr1:246591815-246592267	IMR90	lung:	n/a	n/a
43	CEBPB	chr1:246559741-246559980	HepG2	liver:	n/a	chr1:246559829-246559842 chr1:246559829-246559842 chr1:246559830-246559841
44	CEBPB	chr1:246559718-246559917	A549	lung:	n/a	chr1:246559829-246559842 chr1:246559829-246559842 chr1:246559830-246559841
45	CEBPB	chr1:246591895-246592281	K562	blood:	n/a	n/a
46	CEBPB	chr1:246530442-246530743	IMR90	lung:	n/a	n/a
47	CEBPD	chr1:246591700-246592270	K562	blood:	n/a	n/a
48	CEBPD	chr1:246588359-246589002	K562	blood:	n/a	n/a
49	CEBPD	chr1:246588409-246588903	K562	blood:	n/a	n/a
50	CHD2	chr1:246576797-246577088	K562	blood:	n/a	n/a

(count:427 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:246580717-246580767	HRCEpiC	kidney:	n/a
2	chr1:246580717-246580767	NB4	blood:	n/a
3	chr1:246581705-246581755	LNCaP	prostate:	n/a
4	chr1:246582116-246582166	Jurkat	blood:	n/a
5	chr1:246582116-246582166	MCF10A-Er-Src	breast:	n/a
6	chr1:246582071-246582121	A549	lung:	n/a
7	chr1:246599230-246599280	PrEC	prostate:	n/a
8	chr1:246592123-246592173	T-47D	breast:	n/a
9	chr1:246599230-246599280	GM12892	blood:	n/a
10	chr1:246582116-246582166	U87	brain:	n/a
11	chr1:246580717-246580767	HPAEpiC	pulmonary alveolar:	n/a
12	chr1:246592123-246592173	ECC-1	luminal epithelium:	n/a
13	chr1:246582035-246582085	HCF	heart:	n/a
14	chr1:246582071-246582121	HPAEpiC	pulmonary alveolar:	n/a
15	chr1:246582116-246582166	NHBE	bronchial:	n/a
16	chr1:246599230-246599280	NT2-D1	testis:	n/a
17	chr1:246580717-246580767	LNCaP	prostate:	n/a
18	chr1:246592123-246592173	AG04449	skin:	fetal
19	chr1:246582035-246582085	HIPEpiC	eye:	n/a
20	chr1:246582071-246582121	HepG2	liver:	n/a
21	chr1:246581705-246581755	CMK	blood:	n/a
22	chr1:246582071-246582121	AG09319	gingival:	n/a
23	chr1:246599230-246599280	T-47D	breast:	n/a
24	chr1:246599230-246599280	HRPEpiC	eye:	n/a
25	chr1:246582071-246582121	HL-60	blood:	n/a
26	chr1:246599230-246599280	NB4	blood:	n/a
27	chr1:246582116-246582166	HIPEpiC	eye:	n/a
28	chr1:246582116-246582166	LNCaP	prostate:	n/a
29	chr1:246592123-246592173	HRCEpiC	kidney:	n/a
30	chr1:246582035-246582085	GM12878	blood:	n/a
31	chr1:246592123-246592173	HNPCEpiC	eye:	n/a
32	chr1:246592123-246592173	U87	brain:	n/a
33	chr1:246582071-246582121	ovcar-3	ovarian:	n/a
34	chr1:246582071-246582121	Hepatocyte	liver:	n/a
35	chr1:246581705-246581755	HL-60	blood:	n/a
36	chr1:246580717-246580767	AG09309	skin:	n/a
37	chr1:246581705-246581755	NHBE	bronchial:	n/a
38	chr1:246582035-246582085	PANC-1	pancreas:	n/a
39	chr1:246582035-246582085	T-47D	breast:	n/a
40	chr1:246581705-246581755	AG09319	gingival:	n/a
41	chr1:246582116-246582166	RPTEC	kidney:	n/a
42	chr1:246592123-246592173	PANC-1	pancreas:	n/a
43	chr1:246582035-246582085	SK-N-SH	brain:	n/a
44	chr1:246582116-246582166	BE2_C	brain:	n/a
45	chr1:246580717-246580767	ECC-1	luminal epithelium:	n/a
46	chr1:246582071-246582121	NHBE	bronchial:	n/a
47	chr1:246580717-246580767	HCF	heart:	n/a
48	chr1:246592123-246592173	BJ	skin:	n/a
49	chr1:246582071-246582121	GM12878	blood:	n/a
50	chr1:246599230-246599280	HEEpiC	esophagus:	n/a

(count:26 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:246546236..246548052-chr1:246554234..246556624,2	MCF-7	breast:
2	chr1:246546236..246548052-chr1:246554234..246556624,2	MCF-7	breast:
3	chr1:246582285..246585491-chr1:246585683..246590369,6	K562	blood:
4	chr1:246544799..246546719-chr1:246549229..246551594,2	K562	blood:
5	chr1:246576999..246579498-chr1:246580594..246582855,2	K562	blood:
6	chr1:246548799..246550495-chr1:246559308..246561111,2	K562	blood:
7	chr1:246600615..246602867-chr1:246611265..246613184,2	K562	blood:
8	chr1:246513912..246515911-chr1:246530351..246532425,2	K562	blood:
9	chr1:246601398..246602968-chr1:246608645..246610386,2	K562	blood:
10	chr1:246601270..246602898-chr1:246608886..246610495,2	K562	blood:
11	chr1:246553361..246555954-chr1:246559201..246561583,2	K562	blood:
12	chr1:246579015..246582043-chr1:246583981..246587038,3	K562	blood:
13	chr1:246544799..246546719-chr1:246549229..246551594,2	K562	blood:
14	chr1:246470110..246471825-chr1:246585890..246587442,2	K562	blood:
15	chr1:246594102..246596959-chr1:246598193..246600594,2	K562	blood:
16	chr1:246606314..246608137-chr1:246622294..246625192,2	K562	blood:
17	chr1:246540059..246542497-chr1:246543085..246545736,2	K562	blood:
18	chr1:246536157..246539066-chr1:246540727..246542818,2	K562	blood:
19	chr1:246489256..246490981-chr1:246569694..246571729,2	K562	blood:
20	chr1:246594102..246596959-chr1:246598193..246600594,2	K562	blood:
21	chr1:246540059..246542497-chr1:246543085..246545736,2	K562	blood:
22	chr1:246536157..246539066-chr1:246540727..246542818,2	K562	blood:
23	chr1:246444872..246446533-chr1:246597803..246600502,2	MCF-7	breast:
24	chr1:246553361..246555954-chr1:246559201..246561583,2	K562	blood:
25	chr1:246587797..246590207-chr1:246590613..246593809,3	K562	blood:
26	chr1:246548799..246550495-chr1:246559308..246561111,2	K562	blood:

No data

Variant related genes	Relation type
SMYD3	TF binding region
ENSG00000207326	TF binding region
SMYD3	CpG island
ENSG00000207326	CpG island
ENSG00000207326	chromatin interactions
ENSG00000185420	chromatin interactions

Extended variants
information (count: 3072 )
Associated
traits (count: 88 )

Variant overlapped rSNPs/rCNVs (count:3072 , 50 per page) page: 1 2 3 4 5 6 7 ... 62

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs577729167	chr1:246530468-246530469	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs543495514	chr1:246530494-246530495	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs557147830	chr1:246530508-246530509	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs9970533	chr1:246530522-246530523	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs542946865	chr1:246530567-246530568	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs146857561	chr1:246530612-246530613	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs61841318	chr1:246530620-246530621	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs569756455	chr1:246530680-246530681	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs545039529	chr1:246530698-246530699	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs564858898	chr1:246530711-246530712	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs530653622	chr1:246530816-246530817	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs201942287	chr1:246530882-246530883	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs550404014	chr1:246530892-246530893	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs570273008	chr1:246530908-246530909	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs530686978	chr1:246530920-246530921	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs60264794	chr1:246530945-246530946	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs532022226	chr1:246530976-246530977	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs142573922	chr1:246531063-246531064	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs150944851	chr1:246531075-246531076	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs367595657	chr1:246531079-246531080	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs374340330	chr1:246531120-246531121	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs368188185	chr1:246531122-246531123	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs571286046	chr1:246531160-246531161	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs568562446	chr1:246531179-246531180	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs115781182	chr1:246531257-246531258	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs75922606	chr1:246531264-246531265	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs371582236	chr1:246531265-246531266	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs535878322	chr1:246531274-246531275	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs375230481	chr1:246531365-246531366	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs187244582	chr1:246531420-246531421	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs554191309	chr1:246531447-246531448	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs542480495	chr1:246531449-246531450	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs553171061	chr1:246531452-246531453	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs573209994	chr1:246531462-246531463	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs545302276	chr1:246531491-246531492	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs12095864	chr1:246531497-246531498	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs191862630	chr1:246531531-246531532	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs184399660	chr1:246531561-246531562	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs78877512	chr1:246531610-246531611	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs187730340	chr1:246531612-246531613	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs549324836	chr1:246531647-246531648	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs12060678	chr1:246531703-246531704	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs145809250	chr1:246531763-246531764	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs551653772	chr1:246531848-246531849	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs34588691	chr1:246531865-246531866	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs541336911	chr1:246531967-246531968	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs537058473	chr1:246531989-246531990	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs200272549	chr1:246531996-246531997	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs193249539	chr1:246532012-246532013	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs567670885	chr1:246532014-246532015	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:88)

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
Non-syndromic sensorineural hearing loss	19036926	CNVD

Chromatin state (count:480 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:246514400-246554200	Weak transcription	Primary T cells from cord blood	blood
2	chr1:246520600-246563800	Weak transcription	Osteobl	bone
3	chr1:246529400-246536000	Weak transcription	Ovary	ovary
4	chr1:246535400-246535800	Enhancers	iPS-15b Cell Line	embryonic stem cell
5	chr1:246535400-246536200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr1:246535600-246536200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
7	chr1:246535800-246536200	Enhancers	Psoas Muscle	Psoas
8	chr1:246535800-246536200	Enhancers	Right Atrium	heart
9	chr1:246535800-246536200	Enhancers	Sigmoid Colon	Sigmoid Colon
10	chr1:246535800-246536200	Enhancers	K562	blood
11	chr1:246536000-246536200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr1:246536000-246536200	Enhancers	Ovary	ovary
13	chr1:246536200-246537000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
14	chr1:246536200-246537200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
15	chr1:246536200-246537600	Weak transcription	Ovary	ovary
16	chr1:246536200-246537600	Weak transcription	K562	blood
17	chr1:246536200-246541000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
18	chr1:246536800-246537800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
19	chr1:246537000-246538000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
20	chr1:246537200-246537600	Enhancers	Cortex derived primary cultured neurospheres	brain
21	chr1:246537200-246537600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
22	chr1:246537200-246537800	Enhancers	Brain Hippocampus Middle	brain
23	chr1:246537200-246537800	Enhancers	Brain Substantia Nigra	brain
24	chr1:246537200-246537800	Enhancers	Fetal Lung	lung
25	chr1:246537400-246537800	Enhancers	Brain Angular Gyrus	brain
26	chr1:246537400-246537800	Enhancers	Brain Anterior Caudate	brain
27	chr1:246537400-246537800	Enhancers	Brain Inferior Temporal Lobe	brain
28	chr1:246537600-246538000	Enhancers	Ovary	ovary
29	chr1:246537600-246538000	Enhancers	K562	blood
30	chr1:246537600-246541000	Weak transcription	Cortex derived primary cultured neurospheres	brain
31	chr1:246538000-246541200	Weak transcription	K562	blood
32	chr1:246538000-246547200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
33	chr1:246541000-246541400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
34	chr1:246541000-246541600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr1:246541000-246541600	Enhancers	Cortex derived primary cultured neurospheres	brain
36	chr1:246541000-246541600	Enhancers	Sigmoid Colon	Sigmoid Colon
37	chr1:246541000-246542000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
38	chr1:246541200-246541400	ZNF genes & repeats	K562	blood
39	chr1:246544000-246544200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
40	chr1:246544600-246546000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
41	chr1:246544800-246545400	Enhancers	A549	lung
42	chr1:246545200-246546400	Enhancers	Lung	lung
43	chr1:246545400-246546600	Weak transcription	A549	lung
44	chr1:246545600-246545800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
45	chr1:246545800-246546600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
46	chr1:246545800-246561000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
47	chr1:246546000-246546200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
48	chr1:246546000-246547400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
49	chr1:246546000-246547400	Enhancers	HMEC	breast
50	chr1:246546200-246546400	Flanking Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived

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