Variant report

Variant	nsv998644
Chromosome Location	chr1:246562080-246636600
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:662)
CpG islands
(count:671)
Chromatin interactive
region (count:24)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:662 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:246614088-246614383	HepG2	liver:	n/a	chr1:246614110-246614126
2	ARID3A	chr1:246614048-246614417	K562	blood:	n/a	chr1:246614110-246614126
3	ARID3A	chr1:246587912-246588291	K562	blood:	n/a	n/a
4	ARID3A	chr1:246591789-246592119	K562	blood:	n/a	n/a
5	ATF1	chr1:246589653-246589853	K562	blood:	n/a	n/a
6	ATF1	chr1:246588435-246588914	K562	blood:	n/a	n/a
7	ATF1	chr1:246591887-246592268	K562	blood:	n/a	n/a
8	ATF2	chr1:246598868-246599249	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr1:246606450-246606451	K562	blood:	n/a	n/a
10	BACH1	chr1:246591894-246592194	K562	blood:	n/a	n/a
11	BATF	chr1:246591816-246592158	GM12878	blood:	n/a	n/a
12	BATF	chr1:246591880-246592213	GM12878	blood:	n/a	n/a
13	BCL11A	chr1:246591909-246592164	GM12878	blood:	n/a	n/a
14	BCL11A	chr1:246591893-246592220	GM12878	blood:	n/a	n/a
15	BHLHE40	chr1:246580932-246580933	K562	blood:	n/a	n/a
16	BHLHE40	chr1:246591822-246592280	K562	blood:	n/a	n/a
17	BHLHE40	chr1:246588462-246588796	K562	blood:	n/a	n/a
18	BRCA1	chr1:246598938-246599254	H1-hESC	embryonic stem cell:	n/a	n/a
19	BRCA1	chr1:246622436-246622858	H1-hESC	embryonic stem cell:	n/a	n/a
20	CBX3	chr1:246591794-246592269	K562	blood:	n/a	n/a
21	CBX3	chr1:246582052-246582537	K562	blood:	n/a	n/a
22	CBX3	chr1:246611654-246611998	K562	blood:	n/a	n/a
23	CBX3	chr1:246580386-246580871	K562	blood:	n/a	n/a
24	CBX3	chr1:246576729-246577165	K562	blood:	n/a	n/a
25	CBX3	chr1:246581941-246582555	K562	blood:	n/a	n/a
26	CBX3	chr1:246588426-246589002	K562	blood:	n/a	n/a
27	CBX3	chr1:246591771-246592290	K562	blood:	n/a	n/a
28	CCNT2	chr1:246588441-246589002	K562	blood:	n/a	n/a
29	CEBPB	chr1:246624828-246625147	IMR90	lung:	n/a	chr1:246624986-246624997
30	CEBPB	chr1:246598418-246598737	HepG2	liver:	n/a	chr1:246598665-246598678
31	CEBPB	chr1:246567569-246567749	HepG2	liver:	n/a	n/a
32	CEBPB	chr1:246591895-246592281	K562	blood:	n/a	n/a
33	CEBPB	chr1:246633988-246634252	Hela-S3	cervix:	n/a	chr1:246634078-246634089
34	CEBPB	chr1:246591783-246592270	K562	blood:	n/a	n/a
35	CEBPB	chr1:246633906-246634251	HepG2	liver:	n/a	chr1:246634078-246634089
36	CEBPB	chr1:246624876-246625076	K562	blood:	n/a	chr1:246624986-246624997
37	CEBPB	chr1:246598407-246599012	IMR90	lung:	n/a	chr1:246598811-246598823 chr1:246598665-246598678
38	CEBPB	chr1:246567585-246567742	K562	blood:	n/a	n/a
39	CEBPB	chr1:246614101-246614437	Hela-S3	cervix:	n/a	n/a
40	CEBPB	chr1:246598435-246599408	H1-hESC	embryonic stem cell:	n/a	chr1:246598811-246598823 chr1:246598665-246598678
41	CEBPB	chr1:246588404-246588847	K562	blood:	n/a	n/a
42	CEBPB	chr1:246598404-246598904	A549	lung:	n/a	chr1:246598811-246598823 chr1:246598665-246598678
43	CEBPB	chr1:246614170-246614380	A549	lung:	n/a	n/a
44	CEBPB	chr1:246624890-246625084	HepG2	liver:	n/a	chr1:246624986-246624997
45	CEBPB	chr1:246633942-246634262	K562	blood:	n/a	chr1:246634078-246634089
46	CEBPB	chr1:246598491-246599425	Hela-S3	cervix:	n/a	chr1:246598811-246598823 chr1:246598665-246598678
47	CEBPB	chr1:246633921-246634267	IMR90	lung:	n/a	chr1:246634078-246634089
48	CEBPB	chr1:246591815-246592267	IMR90	lung:	n/a	n/a
49	CEBPB	chr1:246633927-246634250	A549	lung:	n/a	chr1:246634078-246634089
50	CEBPB	chr1:246624833-246625067	HepG2	liver:	n/a	chr1:246624986-246624997

(count:671 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:246582116-246582166	IMR90	lung:	fetal
2	chr1:246599230-246599280	CMK	blood:	n/a
3	chr1:246582116-246582166	PANC-1	pancreas:	n/a
4	chr1:246592123-246592173	A549	lung:	n/a
5	chr1:246613311-246613361	SAEC	small airway:	n/a
6	chr1:246622483-246622533	A549	lung:	n/a
7	chr1:246613311-246613361	SKMC	muscle:	n/a
8	chr1:246599230-246599280	GM06990	blood:	n/a
9	chr1:246581705-246581755	HMEC	breast:	n/a
10	chr1:246580717-246580767	NT2-D1	testis:	n/a
11	chr1:246622633-246622683	AG04450	lung:	fetal
12	chr1:246582071-246582121	PrEC	prostate:	n/a
13	chr1:246580717-246580767	GM12891	blood:	n/a
14	chr1:246622633-246622683	ECC-1	luminal epithelium:	n/a
15	chr1:246582035-246582085	HCT-116	colon:	n/a
16	chr1:246582116-246582166	ProgFib	skin:	n/a
17	chr1:246580717-246580767	HPAEpiC	pulmonary alveolar:	n/a
18	chr1:246581705-246581755	BE2_C	brain:	n/a
19	chr1:246582071-246582121	T-47D	breast:	n/a
20	chr1:246613311-246613361	AG09319	gingival:	n/a
21	chr1:246599230-246599280	GM19239	blood:	n/a
22	chr1:246622662-246622712	AG04449	skin:	fetal
23	chr1:246581705-246581755	RPTEC	kidney:	n/a
24	chr1:246613311-246613361	NHBE	bronchial:	n/a
25	chr1:246622483-246622533	Hepatocyte	liver:	n/a
26	chr1:246582116-246582166	SK-N-MC	brain:	n/a
27	chr1:246580717-246580767	HCT-116	colon:	n/a
28	chr1:246622662-246622712	PANC-1	pancreas:	n/a
29	chr1:246582071-246582121	Hepatocyte	liver:	n/a
30	chr1:246622633-246622683	PFSK-1	brain:	n/a
31	chr1:246582116-246582166	AG09319	gingival:	n/a
32	chr1:246622662-246622712	HCM	heart:	n/a
33	chr1:246581705-246581755	AG09319	gingival:	n/a
34	chr1:246622633-246622683	GM12891	blood:	n/a
35	chr1:246582116-246582166	HMEC	breast:	n/a
36	chr1:246622662-246622712	H1-hESC	embryonic stem cell:	embryo
37	chr1:246581705-246581755	SK-N-SH_RA	brain:	n/a
38	chr1:246613311-246613361	Hela-S3	cervix:	n/a
39	chr1:246582071-246582121	NT2-D1	testis:	n/a
40	chr1:246582071-246582121	LNCaP	prostate:	n/a
41	chr1:246580717-246580767	GM19239	blood:	n/a
42	chr1:246582071-246582121	Jurkat	blood:	n/a
43	chr1:246580717-246580767	SK-N-SH	brain:	n/a
44	chr1:246581705-246581755	HL-60	blood:	n/a
45	chr1:246582116-246582166	HCM	heart:	n/a
46	chr1:246580717-246580767	Caco-2	colon:	n/a
47	chr1:246581705-246581755	NHDF-neo	bronchial:	n/a
48	chr1:246622483-246622533	SK-N-SH	brain:	n/a
49	chr1:246613311-246613361	AoSMC	blood vessel:	n/a
50	chr1:246582035-246582085	ovcar-3	ovarian:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr1:246579015..246582043-chr1:246583981..246587038,3	K562	blood:
2	chr1:246280440..246281134-chr1:246613800..246614445,2	MCF-7	breast:
3	chr1:246576999..246579498-chr1:246580594..246582855,2	K562	blood:
4	chr1:246587797..246590207-chr1:246590613..246593809,3	K562	blood:
5	chr1:246606314..246608137-chr1:246622294..246625192,2	K562	blood:
6	chr1:246635326..246636965-chr1:246661670..246663284,2	K562	blood:
7	chr1:246606314..246608137-chr1:246622294..246625192,2	K562	blood:
8	chr1:246594102..246596959-chr1:246598193..246600594,2	K562	blood:
9	chr1:246600615..246602867-chr1:246611265..246613184,2	K562	blood:
10	chr1:246618350..246620200-chr1:246622120..246624573,2	K562	blood:
11	chr1:246489256..246490981-chr1:246569694..246571729,2	K562	blood:
12	chr1:246470110..246471825-chr1:246585890..246587442,2	K562	blood:
13	chr1:246601270..246602898-chr1:246608886..246610495,2	K562	blood:
14	chr1:246444872..246446533-chr1:246597803..246600502,2	MCF-7	breast:
15	chr1:246601398..246602968-chr1:246608645..246610386,2	K562	blood:
16	chr1:246618350..246620200-chr1:246622120..246624573,2	K562	blood:
17	chr1:246600615..246602867-chr1:246611265..246613184,2	K562	blood:
18	chr1:246175508..246176198-chr1:246613763..246614605,2	K562	blood:
19	chr1:246175245..246176233-chr1:246613342..246615151,4	MCF-7	breast:
20	chr1:246601270..246602898-chr1:246608886..246610495,2	K562	blood:
21	chr1:246594102..246596959-chr1:246598193..246600594,2	K562	blood:
22	chr1:246174027..246176471-chr1:246609850..246611898,2	K562	blood:
23	chr1:246601398..246602968-chr1:246608645..246610386,2	K562	blood:
24	chr1:246582285..246585491-chr1:246585683..246590369,6	K562	blood:

No data

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

Extended variants
information (count: 2873 )
Associated
traits (count: 88 )

Variant overlapped rSNPs/rCNVs (count:2873 , 50 per page) page: 1 2 3 4 5 6 7 ... 58

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7517368	chr1:246562080-246562081	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs375438503	chr1:246562131-246562132	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs189109700	chr1:246562153-246562154	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs531994798	chr1:246562155-246562156	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs191482497	chr1:246562246-246562247	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs150546122	chr1:246562253-246562254	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs199688941	chr1:246562258-246562259	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs562473930	chr1:246562259-246562260	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs185054495	chr1:246562260-246562261	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs386641721	chr1:246562261-246562262	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs201530814	chr1:246562262-246562263	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs150789887	chr1:246562347-246562348	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs541237267	chr1:246562356-246562357	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs7555587	chr1:246562391-246562392	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs10924719	chr1:246562452-246562453	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs369365656	chr1:246562481-246562482	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs7548956	chr1:246562490-246562491	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs76244157	chr1:246562537-246562538	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs145428608	chr1:246562555-246562556	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs565896602	chr1:246562577-246562578	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs35631127	chr1:246562596-246562597	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs189116927	chr1:246562695-246562696	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs376574057	chr1:246562708-246562709	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs181012850	chr1:246562753-246562754	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs538346028	chr1:246562781-246562782	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs369825519	chr1:246562814-246562815	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs377764645	chr1:246562828-246562829	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs574312089	chr1:246562881-246562882	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs144252434	chr1:246562892-246562893	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs560050587	chr1:246562895-246562896	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs186043635	chr1:246562927-246562928	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs12691530	chr1:246562934-246562935	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs114482596	chr1:246562945-246562946	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs531171119	chr1:246562976-246562977	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs548272827	chr1:246563045-246563046	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs148708305	chr1:246563186-246563187	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs9787259	chr1:246563187-246563188	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs564841562	chr1:246563211-246563212	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs6696974	chr1:246563246-246563247	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs74367074	chr1:246563301-246563302	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs559638105	chr1:246563354-246563355	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs367773313	chr1:246563393-246563394	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs539327181	chr1:246563401-246563402	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs532102526	chr1:246563433-246563434	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs80014488	chr1:246563498-246563499	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs540683489	chr1:246563523-246563524	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs112957096	chr1:246563531-246563532	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs181950231	chr1:246563543-246563544	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs568199243	chr1:246563560-246563561	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs533767492	chr1:246563595-246563596	Weak transcription Enhancers	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:492 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:246520600-246563800	Weak transcription	Osteobl	bone
2	chr1:246554600-246594800	Weak transcription	Right Ventricle	heart
3	chr1:246557200-246590800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr1:246559200-246568800	Weak transcription	Lung	lung
5	chr1:246560200-246580600	Weak transcription	Primary T cells from cord blood	blood
6	chr1:246560400-246580200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
7	chr1:246561400-246562200	Enhancers	HepG2	liver
8	chr1:246562000-246562200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr1:246562000-246567200	Weak transcription	K562	blood
10	chr1:246563400-246564400	Enhancers	Muscle Satellite Cultured Cells	--
11	chr1:246563600-246564200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
12	chr1:246563800-246564000	Enhancers	Osteobl	bone
13	chr1:246564000-246564200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
14	chr1:246564000-246564400	Enhancers	HUVEC	blood vessel
15	chr1:246564000-246564400	Weak transcription	Osteobl	bone
16	chr1:246564400-246564600	Enhancers	Osteobl	bone
17	chr1:246564600-246578400	Weak transcription	Osteobl	bone
18	chr1:246564800-246565200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
19	chr1:246566400-246566600	Enhancers	Gastric	stomach
20	chr1:246566600-246567200	Weak transcription	Gastric	stomach
21	chr1:246567000-246567400	Enhancers	Pancreatic Islets	Pancreatic Islet
22	chr1:246567200-246567800	Enhancers	Gastric	stomach
23	chr1:246567200-246567800	Enhancers	K562	blood
24	chr1:246567200-246568000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr1:246567400-246567800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
26	chr1:246567400-246568000	Weak transcription	Pancreatic Islets	Pancreatic Islet
27	chr1:246567600-246568000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
28	chr1:246567600-246568400	Enhancers	NHDF-Ad	bronchial
29	chr1:246568000-246568200	Enhancers	Pancreatic Islets	Pancreatic Islet
30	chr1:246568000-246578400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
31	chr1:246571000-246580400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
32	chr1:246573000-246576800	Weak transcription	Aorta	Aorta
33	chr1:246575400-246575600	ZNF genes & repeats	Dnd41	blood
34	chr1:246575800-246580200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
35	chr1:246576400-246588600	Weak transcription	H9 Cell Line	embryonic stem cell
36	chr1:246576600-246577400	Enhancers	K562	blood
37	chr1:246576800-246577200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
38	chr1:246576800-246577200	ZNF genes & repeats	Aorta	Aorta
39	chr1:246577000-246577200	Enhancers	iPS-15b Cell Line	embryonic stem cell
40	chr1:246577000-246577200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
41	chr1:246577200-246588600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
42	chr1:246577200-246588600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
43	chr1:246577200-246588600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
44	chr1:246577400-246577600	Enhancers	Cortex derived primary cultured neurospheres	brain
45	chr1:246578400-246578800	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
46	chr1:246578400-246578800	Flanking Active TSS	Osteobl	bone
47	chr1:246578600-246580200	Enhancers	NHDF-Ad	bronchial
48	chr1:246578800-246579600	Active TSS	Osteobl	bone
49	chr1:246578800-246579800	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
50	chr1:246578800-246584000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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