Variant report

Variant	nsv873413
Chromosome Location	chr1:246364811-246475061
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1152)
CpG islands
(count:978)
Chromatin interactive
region (count:70)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1152 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:246378134-246379212	K562	blood:	n/a	n/a
2	ARID3A	chr1:246444896-246445377	HepG2	liver:	n/a	n/a
3	ARID3A	chr1:246383173-246383457	HepG2	liver:	n/a	n/a
4	ARID3A	chr1:246443886-246444158	K562	blood:	n/a	n/a
5	ARID3A	chr1:246472537-246472962	K562	blood:	n/a	n/a
6	ARID3A	chr1:246469874-246470465	K562	blood:	n/a	n/a
7	ARID3A	chr1:246378433-246378571	HepG2	liver:	n/a	n/a
8	ARID3A	chr1:246468839-246469426	K562	blood:	n/a	n/a
9	ARID3A	chr1:246409804-246409947	K562	blood:	n/a	n/a
10	ATF1	chr1:246376288-246376805	K562	blood:	n/a	n/a
11	ATF1	chr1:246370614-246370654	K562	blood:	n/a	n/a
12	ATF1	chr1:246469981-246470295	K562	blood:	n/a	n/a
13	ATF1	chr1:246378205-246378667	K562	blood:	n/a	n/a
14	ATF1	chr1:246445017-246445192	K562	blood:	n/a	n/a
15	ATF2	chr1:246378137-246378580	GM12878	blood:	n/a	n/a
16	ATF2	chr1:246378108-246378612	GM12878	blood:	n/a	n/a
17	ATF3	chr1:246378129-246378678	K562	blood:	n/a	n/a
18	BACH1	chr1:246383042-246383141	H1-hESC	embryonic stem cell:	n/a	n/a
19	BACH1	chr1:246426231-246426459	H1-hESC	embryonic stem cell:	n/a	n/a
20	BACH1	chr1:246378344-246378673	K562	blood:	n/a	n/a
21	BACH1	chr1:246469627-246470581	K562	blood:	n/a	n/a
22	BACH1	chr1:246469042-246469374	H1-hESC	embryonic stem cell:	n/a	n/a
23	BACH1	chr1:246469926-246470676	H1-hESC	embryonic stem cell:	n/a	n/a
24	BACH1	chr1:246469053-246469366	K562	blood:	n/a	n/a
25	BATF	chr1:246411492-246411928	GM12878	blood:	n/a	n/a
26	BATF	chr1:246378267-246378548	GM12878	blood:	n/a	n/a
27	BATF	chr1:246378240-246378549	GM12878	blood:	n/a	n/a
28	BCL11A	chr1:246378236-246378598	GM12878	blood:	n/a	n/a
29	BCL11A	chr1:246378302-246378519	GM12878	blood:	n/a	n/a
30	BCL3	chr1:246474759-246475054	GM12878	blood:	n/a	n/a
31	BCLAF1	chr1:246378155-246378681	GM12878	blood:	n/a	n/a
32	BHLHE40	chr1:246469899-246470287	K562	blood:	n/a	n/a
33	BHLHE40	chr1:246377992-246378738	K562	blood:	n/a	n/a
34	BHLHE40	chr1:246378250-246378658	GM12878	blood:	n/a	n/a
35	BHLHE40	chr1:246383064-246383373	HepG2	liver:	n/a	n/a
36	BHLHE40	chr1:246376557-246377048	K562	blood:	n/a	n/a
37	BRCA1	chr1:246383162-246383283	HepG2	liver:	n/a	n/a
38	CBX3	chr1:246378003-246379187	K562	blood:	n/a	n/a
39	CBX3	chr1:246383961-246384329	K562	blood:	n/a	n/a
40	CBX3	chr1:246378198-246378843	K562	blood:	n/a	n/a
41	CBX3	chr1:246382525-246383196	K562	blood:	n/a	n/a
42	CBX3	chr1:246469834-246470418	K562	blood:	n/a	n/a
43	CBX3	chr1:246383779-246384415	K562	blood:	n/a	n/a
44	CBX3	chr1:246469114-246469749	K562	blood:	n/a	chr1:246469383-246469394
45	CBX3	chr1:246421618-246421974	HCT-116	colon:	n/a	n/a
46	CBX3	chr1:246421526-246421879	K562	blood:	n/a	n/a
47	CCNT2	chr1:246472666-246473033	K562	blood:	n/a	n/a
48	CCNT2	chr1:246378279-246379042	K562	blood:	n/a	n/a
49	CCNT2	chr1:246470003-246470249	K562	blood:	n/a	n/a
50	CEBPB	chr1:246378236-246378755	K562	blood:	n/a	chr1:246378505-246378516 chr1:246378504-246378517

(count:978 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:246429789-246429839	HNPCEpiC	eye:	n/a
2	chr1:246414665-246414715	HEK293	kidney:	embryo
3	chr1:246429789-246429839	HNPCEpiC	eye:	n/a
4	chr1:246414665-246414715	HEK293	kidney:	embryo
5	chr1:246415165-246415215	ovcar-3	ovarian:	n/a
6	chr1:246446300-246446350	HUVEC	blood vessel:	n/a
7	chr1:246414665-246414715	HRPEpiC	eye:	n/a
8	chr1:246466280-246466330	GM19239	blood:	n/a
9	chr1:246466280-246466330	U87	brain:	n/a
10	chr1:246414665-246414715	HCM	heart:	n/a
11	chr1:246415214-246415264	HCF	heart:	n/a
12	chr1:246415176-246415226	HMEC	breast:	n/a
13	chr1:246414665-246414715	NT2-D1	testis:	n/a
14	chr1:246370933-246370983	K562	blood:	n/a
15	chr1:246415176-246415226	SK-N-SH	brain:	n/a
16	chr1:246415165-246415215	HNPCEpiC	eye:	n/a
17	chr1:246451744-246451794	GM19239	blood:	n/a
18	chr1:246415214-246415264	LNCaP	prostate:	n/a
19	chr1:246457244-246457294	BJ	skin:	n/a
20	chr1:246446300-246446350	RPTEC	kidney:	n/a
21	chr1:246414665-246414715	GM12892	blood:	n/a
22	chr1:246416688-246416738	Jurkat	blood:	n/a
23	chr1:246383021-246383071	AG04450	lung:	fetal
24	chr1:246415568-246415618	ProgFib	skin:	n/a
25	chr1:246416688-246416738	HRPEpiC	eye:	n/a
26	chr1:246457244-246457294	SK-N-SH	brain:	n/a
27	chr1:246451744-246451794	HCPEpiC	choroid plexus:	n/a
28	chr1:246378510-246378560	U87	brain:	n/a
29	chr1:246378510-246378560	HMEC	breast:	n/a
30	chr1:246414665-246414715	PrEC	prostate:	n/a
31	chr1:246416688-246416738	MCF-7	breast:	n/a
32	chr1:246415568-246415618	LNCaP	prostate:	n/a
33	chr1:246415214-246415264	GM12891	blood:	n/a
34	chr1:246415176-246415226	GM19239	blood:	n/a
35	chr1:246414665-246414715	SK-N-SH	brain:	n/a
36	chr1:246466280-246466330	PANC-1	pancreas:	n/a
37	chr1:246415568-246415618	MCF-7	breast:	n/a
38	chr1:246416688-246416738	HEEpiC	esophagus:	n/a
39	chr1:246446300-246446350	SK-N-SH	brain:	n/a
40	chr1:246370933-246370983	AG09319	gingival:	n/a
41	chr1:246415165-246415215	HRE	kidney:	n/a
42	chr1:246415214-246415264	PrEC	prostate:	n/a
43	chr1:246414840-246414890	HCM	heart:	n/a
44	chr1:246415214-246415264	HCM	heart:	n/a
45	chr1:246415165-246415215	AG09319	gingival:	n/a
46	chr1:246416688-246416738	RPTEC	kidney:	n/a
47	chr1:246383021-246383071	HNPCEpiC	eye:	n/a
48	chr1:246466280-246466330	MCF-7	breast:	n/a
49	chr1:246466280-246466330	Hepatocyte	liver:	n/a
50	chr1:246415568-246415618	SK-N-SH_RA	brain:	n/a

(count:70 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr1:246175314..246176186-chr1:246443613..246444388,3	K562	blood:
2	chr1:246470110..246471825-chr1:246585890..246587442,2	K562	blood:
3	chr1:246463275..246466123-chr1:246471236..246474164,2	MCF-7	breast:
4	chr1:246355633..246357976-chr1:246377083..246378948,2	K562	blood:
5	chr1:246175573..246176199-chr1:246409475..246409997,2	K562	blood:
6	chr1:246363848..246365407-chr1:246365927..246368390,2	K562	blood:
7	chr1:246356773..246358540-chr1:246441873..246443730,2	K562	blood:
8	chr1:246383754..246387049-chr1:246387673..246391431,4	K562	blood:
9	chr1:246377128..246379304-chr1:246383039..246386771,4	K562	blood:
10	chr1:246358405..246360090-chr1:246368790..246371523,2	K562	blood:
11	chr1:246391990..246394704-chr1:246397912..246399430,2	K562	blood:
12	chr1:246407877..246409674-chr1:246412098..246414077,2	K562	blood:
13	chr1:246389393..246391368-chr1:246392967..246394891,2	K562	blood:
14	chr1:246391990..246394704-chr1:246397912..246399430,2	K562	blood:
15	chr1:246357089..246359442-chr1:246368577..246370809,2	MCF-7	breast:
16	chr1:246331480..246335528-chr1:246374874..246378179,5	K562	blood:
17	chr1:246452108..246454615-chr1:246458116..246460010,2	K562	blood:
18	chr1:246464800..246467604-chr1:246470299..246472286,2	MCF-7	breast:
19	chr1:246374232..246375756-chr1:246376592..246378165,2	K562	blood:
20	chr1:246446720..246449077-chr1:246451672..246454637,2	K562	blood:
21	chr1:246471340..246473899-chr1:246474297..246475919,2	K562	blood:
22	chr1:246471340..246473899-chr1:246474297..246475919,2	K562	blood:
23	chr1:246389393..246391368-chr1:246392967..246395959,3	K562	blood:
24	chr1:246458189..246460474-chr1:246462017..246465759,3	K562	blood:
25	chr1:246463275..246466123-chr1:246471236..246474164,2	MCF-7	breast:
26	chr1:246371493..246375018-chr1:246378492..246381970,3	MCF-7	breast:
27	chr1:246356574..246358892-chr1:246371653..246374292,2	K562	blood:
28	chr1:246345857..246348884-chr1:246378191..246381575,3	K562	blood:
29	chr1:246374232..246375756-chr1:246376592..246378165,2	K562	blood:
30	chr1:246353223..246355045-chr1:246376088..246378374,2	K562	blood:
31	chr1:246377070..246379889-chr1:246380725..246383126,2	MCF-7	breast:
32	chr1:246175301..246176197-chr1:246366037..246366781,3	MCF-7	breast:
33	chr1:246304167..246305671-chr1:246388175..246390464,2	K562	blood:
34	chr1:246389393..246391368-chr1:246392967..246394891,2	K562	blood:
35	chr1:246452108..246454615-chr1:246458116..246460010,2	K562	blood:
36	chr1:246446720..246449077-chr1:246451672..246454637,2	K562	blood:
37	chr1:246185726..246188370-chr1:246444618..246447428,2	K562	blood:
38	chr1:246353361..246355066-chr1:246367112..246369364,2	K562	blood:
39	chr1:246451778..246454398-chr1:246470226..246471898,2	K562	blood:
40	chr1:246464800..246467604-chr1:246470299..246472286,2	MCF-7	breast:
41	chr1:246451778..246454398-chr1:246470226..246471898,2	K562	blood:
42	chr1:246331255..246333673-chr1:246367321..246369174,2	K562	blood:
43	chr1:246339928..246341615-chr1:246379189..246380773,2	K562	blood:
44	chr1:246361048..246363741-chr1:246366833..246369637,3	K562	blood:
45	chr1:246385164..246386821-chr1:246393908..246395594,2	K562	blood:
46	chr1:246377128..246379304-chr1:246383039..246386771,4	K562	blood:
47	chr1:246385164..246386821-chr1:246393908..246395594,2	K562	blood:
48	chr1:246371493..246375018-chr1:246378492..246381970,3	MCF-7	breast:
49	chr1:246304825..246308561-chr1:246370108..246374332,3	K562	blood:
50	chr1:246392871..246395828-chr1:246399439..246401491,2	K562	blood:

No data

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

Extended variants
information (count: 4711 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:4711 , 50 per page) page: 1 2 3 4 5 6 7 ... 95

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12079361	chr1:246364811-246364812	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs183557513	chr1:246364853-246364854	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs113732170	chr1:246364873-246364874	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs186669294	chr1:246364931-246364932	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs142524292	chr1:246364942-246364943	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs535643299	chr1:246365060-246365061	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs552276125	chr1:246365071-246365072	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs576064849	chr1:246365087-246365088	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs145899537	chr1:246365089-246365090	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs568518714	chr1:246365100-246365101	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs531678698	chr1:246365167-246365168	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs548396045	chr1:246365176-246365177	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs1806502	chr1:246365186-246365187	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs534101560	chr1:246365213-246365214	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs374428015	chr1:246365239-246365240	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs552724519	chr1:246365276-246365277	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs143427421	chr1:246365286-246365287	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs75490325	chr1:246365291-246365292	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs11433640	chr1:246365327-246365328	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs116189559	chr1:246365328-246365329	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs556179768	chr1:246365364-246365365	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs141762887	chr1:246365387-246365388	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs190638249	chr1:246365449-246365450	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs377472689	chr1:246365461-246365462	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs574896212	chr1:246365487-246365488	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs572226283	chr1:246365556-246365557	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs539509416	chr1:246365590-246365591	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs370067108	chr1:246365636-246365637	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs111910796	chr1:246365643-246365644	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs374808898	chr1:246365662-246365663	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs540925096	chr1:246365700-246365701	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs144879088	chr1:246365734-246365735	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs2333994	chr1:246365768-246365769	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs78628592	chr1:246365783-246365784	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs562523848	chr1:246365794-246365795	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs182499894	chr1:246365896-246365897	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs544113046	chr1:246365911-246365912	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs187188835	chr1:246365917-246365918	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs561921002	chr1:246365955-246365956	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs12076158	chr1:246366027-246366028	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs12734529	chr1:246366056-246366057	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs12754871	chr1:246366057-246366058	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs12076187	chr1:246366061-246366062	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs12754889	chr1:246366099-246366100	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs557265501	chr1:246366158-246366159	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs570792048	chr1:246366175-246366176	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs189541768	chr1:246366238-246366239	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs549847327	chr1:246366255-246366256	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs12141086	chr1:246366287-246366288	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs76585443	chr1:246366300-246366301	Weak transcription	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
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Bipolar disorder	19114987	CNVD
Schizophrenia	19805367	CNVD

Chromatin state (count:619 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:246314200-246369000	Weak transcription	Aorta	Aorta
2	chr1:246338400-246371400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
3	chr1:246340200-246384600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr1:246342600-246369400	Weak transcription	Fetal Stomach	stomach
5	chr1:246343200-246378400	Weak transcription	Primary T cells from cord blood	blood
6	chr1:246349400-246373000	Weak transcription	Primary hematopoietic stem cells	blood
7	chr1:246350200-246369200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
8	chr1:246363000-246376800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr1:246363000-246377400	Weak transcription	Osteobl	bone
10	chr1:246363200-246368600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr1:246363800-246367400	Weak transcription	Ovary	ovary
12	chr1:246364800-246376000	Weak transcription	K562	blood
13	chr1:246367800-246368600	Enhancers	Placenta Amnion	Placenta Amnion
14	chr1:246368600-246369000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr1:246368600-246370000	Enhancers	Primary monocytes fromperipheralblood	blood
16	chr1:246368800-246369800	Enhancers	Monocytes-CD14+_RO01746	blood
17	chr1:246368800-246372800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
18	chr1:246369000-246369200	Enhancers	Aorta	Aorta
19	chr1:246369000-246373400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
20	chr1:246369000-246374400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
21	chr1:246369200-246370000	Enhancers	Primary hematopoietic stem cells short term culture	blood
22	chr1:246369200-246384000	Weak transcription	Aorta	Aorta
23	chr1:246370800-246373400	Weak transcription	Lung	lung
24	chr1:246371200-246372000	Enhancers	Fetal Lung	lung
25	chr1:246371400-246372200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
26	chr1:246372200-246378400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
27	chr1:246372800-246373200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
28	chr1:246373000-246373800	Enhancers	Primary hematopoietic stem cells	blood
29	chr1:246373200-246374400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chr1:246373400-246373600	Enhancers	Lung	lung
31	chr1:246373400-246374400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
32	chr1:246373800-246374200	Weak transcription	Primary hematopoietic stem cells	blood
33	chr1:246373800-246374600	Enhancers	Fetal Brain Male	brain
34	chr1:246373800-246374800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
35	chr1:246374000-246374200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
36	chr1:246374000-246374200	Active TSS	Fetal Brain Female	brain
37	chr1:246374000-246374200	Enhancers	Pancreatic Islets	Pancreatic Islet
38	chr1:246374000-246374600	Enhancers	iPS-15b Cell Line	embryonic stem cell
39	chr1:246374000-246374600	Enhancers	Cortex derived primary cultured neurospheres	brain
40	chr1:246374000-246374800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr1:246374000-246374800	Enhancers	HUES48 Cell Line	embryonic stem cell
42	chr1:246374000-246374800	Enhancers	HUES6 Cell Line	embryonic stem cell
43	chr1:246374200-246374400	Enhancers	Primary hematopoietic stem cells	blood
44	chr1:246374200-246374400	Flanking Active TSS	Fetal Brain Female	brain
45	chr1:246374200-246374400	Enhancers	Pancreas	Pancrea
46	chr1:246374200-246374600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
47	chr1:246374200-246374600	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet
48	chr1:246374200-246382800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
49	chr1:246374400-246375000	Enhancers	Fetal Brain Female	brain
50	chr1:246374400-246375800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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