Variant report

Variant	esv3319265
Chromosome Location	chr1:10480465-10485563
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:180)
CpG islands
(count:61)
Chromatin interactive
region (count:13)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:180 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BCL3	chr1:10480357-10481022	A549	lung:	n/a	n/a
2	BCL3	chr1:10481065-10485114	A549	lung:	n/a	n/a
3	BCL3	chr1:10483696-10484182	A549	lung:	n/a	n/a
4	BCL3	chr1:10481151-10483619	A549	lung:	n/a	n/a
5	BHLHE40	chr1:10481691-10481732	K562	blood:	n/a	n/a
6	CCNT2	chr1:10480614-10480901	K562	blood:	n/a	n/a
7	CEBPB	chr1:10480685-10480898	K562	blood:	n/a	n/a
8	CEBPB	chr1:10484421-10484841	A549	lung:	n/a	n/a
9	CREB1	chr1:10481782-10482246	A549	lung:	n/a	n/a
10	CTCF	chr1:10482036-10482066	H1-hESC	embryonic stem cell:	n/a	n/a
11	CTCF	chr1:10484080-10484230	HPAF	blood vessel:	n/a	n/a
12	CTCF	chr1:10484100-10484250	AoAF	blood vessel:	n/a	n/a
13	CTCF	chr1:10484020-10484170	HCPEpiC	choroid plexus:	n/a	n/a
14	CTCF	chr1:10484060-10484210	BJ	skin:	n/a	n/a
15	CTCF	chr1:10482012-10482081	A549	lung:	n/a	n/a
16	CTCF	chr1:10482000-10482150	A549	lung:	n/a	n/a
17	CTCF	chr1:10484080-10484230	HBMEC	blood vessel:	n/a	n/a
18	CTCF	chr1:10484160-10484310	NHLF	lung:	n/a	n/a
19	CTCF	chr1:10484120-10484270	AG10803	skin:	n/a	n/a
20	CTCF	chr1:10482013-10482084	MCF-7	breast:	n/a	n/a
21	CTCF	chr1:10481900-10482050	HCPEpiC	choroid plexus:	n/a	n/a
22	CTCF	chr1:10481940-10482090	NHEK	skin:	n/a	n/a
23	CTCF	chr1:10484180-10484330	NHDF-neo	bronchial:	n/a	n/a
24	CTCF	chr1:10484147-10484203	MCF-7	breast:	n/a	n/a
25	CTCF	chr1:10484102-10484233	Fibrobl	skin:	n/a	n/a
26	CTCF	chr1:10484080-10484230	AG09319	gingival:	n/a	n/a
27	CTCF	chr1:10484100-10484250	BJ	skin:	n/a	n/a
28	CTCF	chr1:10484140-10484290	AG09309	skin:	n/a	n/a
29	CTCF	chr1:10484040-10484190	HCPEpiC	choroid plexus:	n/a	n/a
30	CTCF	chr1:10484040-10484190	HPF	lung:	n/a	n/a
31	CTCF	chr1:10484040-10484190	AG04450	lung:	n/a	n/a
32	CTCF	chr1:10484100-10484250	AG04449	skin:	n/a	n/a
33	CTCF	chr1:10484100-10484250	HMF	breast:	n/a	n/a
34	CTCF	chr1:10484120-10484270	HFF	foreskin:	n/a	n/a
35	CTCF	chr1:10482014-10482089	MCF-7	breast:	n/a	n/a
36	CTCF	chr1:10484120-10484270	NHDF-neo	bronchial:	n/a	n/a
37	CTCF	chr1:10482024-10482095	MCF-7	breast:	n/a	n/a
38	CTCF	chr1:10484120-10484270	HMF	breast:	n/a	n/a
39	E2F6	chr1:10484057-10484556	A549	lung:	n/a	n/a
40	EGR1	chr1:10484040-10484286	K562	blood:	n/a	n/a
41	EP300	chr1:10481935-10482472	A549	lung:	n/a	n/a
42	ETS1	chr1:10481342-10481812	A549	lung:	n/a	n/a
43	ETS1	chr1:10481897-10482270	A549	lung:	n/a	n/a
44	FOSL2	chr1:10481217-10481747	A549	lung:	n/a	n/a
45	FOXA1	chr1:10485212-10485540	HepG2	liver:	n/a	n/a
46	FOXA2	chr1:10485326-10485845	A549	lung:	n/a	n/a
47	GATA3	chr1:10481313-10482458	A549	lung:	n/a	n/a
48	GATA3	chr1:10480555-10480782	SH-SY5Y	brain:	n/a	chr1:10480581-10480591
49	HEY1	chr1:10485354-10485514	HepG2	liver:	n/a	n/a
50	JUND	chr1:10481136-10482700	A549	lung:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:10484899-10484949	HCM	heart:	n/a
2	chr1:10484899-10484949	A549	lung:	n/a
3	chr1:10484899-10484949	HUVEC	blood vessel:	n/a
4	chr1:10484899-10484949	HMEC	breast:	n/a
5	chr1:10484899-10484949	HEK293	kidney:	embryo
6	chr1:10484899-10484949	HNPCEpiC	eye:	n/a
7	chr1:10484899-10484949	Jurkat	blood:	n/a
8	chr1:10484899-10484949	MCF10A-Er-Src	breast:	n/a
9	chr1:10484899-10484949	AoSMC	blood vessel:	n/a
10	chr1:10484899-10484949	PrEC	prostate:	n/a
11	chr1:10484899-10484949	HCT-116	colon:	n/a
12	chr1:10484899-10484949	BJ	skin:	n/a
13	chr1:10484899-10484949	PANC-1	pancreas:	n/a
14	chr1:10484899-10484949	AG09309	skin:	n/a
15	chr1:10484899-10484949	GM12878	blood:	n/a
16	chr1:10484899-10484949	LNCaP	prostate:	n/a
17	chr1:10484899-10484949	HIPEpiC	eye:	n/a
18	chr1:10484899-10484949	PFSK-1	brain:	n/a
19	chr1:10484899-10484949	ProgFib	skin:	n/a
20	chr1:10484899-10484949	CMK	blood:	n/a
21	chr1:10484899-10484949	HepG2	liver:	n/a
22	chr1:10484899-10484949	SK-N-SH_RA	brain:	n/a
23	chr1:10484899-10484949	H1-hESC	embryonic stem cell:	embryo
24	chr1:10484899-10484949	HRE	kidney:	n/a
25	chr1:10484899-10484949	HAEpiC	amniotic membrane:	n/a
26	chr1:10484899-10484949	IMR90	lung:	fetal
27	chr1:10484899-10484949	SAEC	small airway:	n/a
28	chr1:10484899-10484949	HL-60	blood:	n/a
29	chr1:10484899-10484949	GM12891	blood:	n/a
30	chr1:10484899-10484949	ECC-1	luminal epithelium:	n/a
31	chr1:10484899-10484949	GM06990	blood:	n/a
32	chr1:10484899-10484949	BE2_C	brain:	n/a
33	chr1:10484899-10484949	NHDF-neo	bronchial:	n/a
34	chr1:10484899-10484949	SK-N-SH	brain:	n/a
35	chr1:10484899-10484949	AG04450	lung:	fetal
36	chr1:10484899-10484949	NHBE	bronchial:	n/a
37	chr1:10484899-10484949	RPTEC	kidney:	n/a
38	chr1:10484899-10484949	HPAEpiC	pulmonary alveolar:	n/a
39	chr1:10484899-10484949	SKMC	muscle:	n/a
40	chr1:10484899-10484949	NH-A	brain:	n/a
41	chr1:10484899-10484949	ovcar-3	ovarian:	n/a
42	chr1:10484899-10484949	GM19239	blood:	n/a
43	chr1:10484899-10484949	GM12892	blood:	n/a
44	chr1:10484899-10484949	U87	brain:	n/a
45	chr1:10484899-10484949	MCF-7	breast:	n/a
46	chr1:10484899-10484949	HCPEpiC	choroid plexus:	n/a
47	chr1:10484899-10484949	AG04449	skin:	fetal
48	chr1:10484899-10484949	HRPEpiC	eye:	n/a
49	chr1:10484899-10484949	Hepatocyte	liver:	n/a
50	chr1:10484899-10484949	HEEpiC	esophagus:	n/a

(count:13 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:10474109..10477987-chr1:10478782..10481616,9	K562	blood:
2	chr1:10479306..10481846-chr1:10534906..10536972,2	K562	blood:
3	chr1:10458949..10460563-chr1:10481035..10483154,2	MCF-7	breast:
4	chr1:10417330..10419820-chr1:10480235..10483214,2	K562	blood:
5	chr1:10474880..10479716-chr1:10481883..10486910,5	K562	blood:
6	chr1:10469567..10472179-chr1:10478906..10481569,2	MCF-7	breast:
7	chr1:10456065..10459752-chr1:10480399..10483247,3	K562	blood:
8	chr1:10475618..10478486-chr1:10479191..10481866,2	MCF-7	breast:
9	chr1:10480824..10482719-chr1:10531236..10533762,2	K562	blood:
10	chr1:10479206..10481807-chr1:10489257..10490879,3	K562	blood:
11	chr1:10474196..10477325-chr1:10477463..10484153,8	K562	blood:
12	chr1:10483316..10484984-chr1:10487772..10489866,2	K562	blood:
13	chr1:10458252..10460577-chr1:10480549..10482459,3	K562	blood:

No data

Variant related genes	Relation type
APITD1	TF binding region
APITD1-CORT	TF binding region
APITD1	CpG island
APITD1-CORT	CpG island
ENSG00000175279	chromatin interactions
ENSG00000142655	chromatin interactions
ENSG00000251503	chromatin interactions
ENSG00000271989	chromatin interactions
ENSG00000160049	chromatin interactions
ENSG00000142657	chromatin interactions

Extended variants
information (count: 260 )
Associated
traits (count: 115 )

Variant overlapped rSNPs/rCNVs (count:260 , 50 per page) page: 1 2 3 4 5 6

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs140049314	chr1:10480468-10480469	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
2	rs397979181	chr1:10480470-10480471	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
3	rs12061972	chr1:10480476-10480477	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
4	rs1134026	chr1:10480482-10480483	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
5	rs534025238	chr1:10480489-10480490	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
6	rs555784165	chr1:10480519-10480520	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
7	rs1140445	chr1:10480521-10480522	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
8	rs567566355	chr1:10480526-10480527	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
9	rs538210538	chr1:10480539-10480540	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
10	rs1140446	chr1:10480542-10480543	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
11	rs556606474	chr1:10480636-10480637	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
12	rs578245717	chr1:10480673-10480674	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
13	rs181468265	chr1:10480677-10480678	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
14	rs71643090	chr1:10480696-10480697	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
15	rs565118933	chr1:10480723-10480724	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
16	rs185756861	chr1:10480745-10480746	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
17	rs35497080	chr1:10480777-10480778	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
18	rs542370300	chr1:10480793-10480794	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
19	rs139949447	chr1:10480818-10480819	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
20	rs377115164	chr1:10480824-10480825	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
21	rs543386090	chr1:10480825-10480826	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
22	rs565069659	chr1:10480839-10480840	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
23	rs532265764	chr1:10480845-10480846	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
24	rs12755363	chr1:10480866-10480867	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
25	rs571273482	chr1:10480920-10480921	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
26	rs561327619	chr1:10480930-10480931	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
27	rs559125947	chr1:10480945-10480946	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
28	rs150763595	chr1:10480947-10480948	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
29	rs190128544	chr1:10480951-10480952	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
30	rs567725610	chr1:10480952-10480953	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
31	rs377192355	chr1:10480960-10480961	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
32	rs550137872	chr1:10480970-10480971	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
33	rs12402723	chr1:10480983-10480984	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
34	rs530827186	chr1:10480984-10480985	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
35	rs181188494	chr1:10480994-10480995	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
36	rs572696251	chr1:10481014-10481015	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
37	rs186226141	chr1:10481021-10481022	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
38	rs554398081	chr1:10481023-10481024	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
39	rs540612192	chr1:10481040-10481041	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
40	rs565569871	chr1:10481068-10481069	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
41	rs190745718	chr1:10481069-10481070	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
42	rs543092370	chr1:10481111-10481112	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
43	rs564536959	chr1:10481128-10481129	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
44	rs550630413	chr1:10481130-10481131	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
45	rs540936464	chr1:10481135-10481136	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
46	rs559193494	chr1:10481142-10481143	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
47	rs184238949	chr1:10481143-10481144	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
48	rs548349253	chr1:10481189-10481190	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
49	rs561263638	chr1:10481191-10481192	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
50	rs531826379	chr1:10481208-10481209	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:115)

Disease	PMID	Source
Glioblastoma multiforme	21080181	CNVD
Follicular lymphoma	18703704	CNVD
Lung cancer	22429812	CNVD
Epilepsy	22118685	CNVD
Schizophrenia	22118685	CNVD
Ovarian cancer	21720365	CNVD
Developmental delay	19490664	CNVD
Ewing''s sarcoma	21437220	CNVD
Prader-willi syndrome	18797701	CNVD
periventricular nodular heterotopia	20648244	CNVD
1p36 deletion syndrome	22283845	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Follicular lymphoma	20505157	CNVD
Neuroblastoma	18923524	CNVD
Retinoblastoma	22278416	CNVD
Mental retardation	20152051	CNVD
Breast cancer	17603634	CNVD
Medulloblastoma	21979893	CNVD
Astrocytoma	17934521	CNVD
Glioblastoma	20031968	CNVD
Acute myeloid leukemia	18000384	CNVD
Glioblastoma multiforme	16951158	CNVD
Neuroblastoma	18574593	CNVD
Glioblastoma multiforme	17369134	CNVD
Autism	18414403	CNVD
Breast cancer	17001317	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Myoepithelioma	18604193	CNVD
Wilms tumour	19047088	CNVD
Breast cancer	16608533	CNVD
T-cell lymphomas	19863542	CNVD
Hepatocellular carcinoma	16750200	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
Breast cancer	17133270	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Metanephric adenoma	20802469	CNVD
Soft tissue tumor	16732325	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Colorectal cancer	16272173	CNVD
Wilms tumour	21544195	CNVD
Coronary Disease	20032323	CNVD
Prostate cancer	21965145	CNVD
Stargardt''s disease	17277736	CNVD
Neuroblastoma	17897457	CNVD
Uveal melanoma	21693616	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Neuroblastoma	21484798	CNVD
Non-syndromic sensorineural hearing loss	22290220	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	21264507	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	17387387	CNVD
Oligodendroglial tumors	17285580	CNVD
Neuroblastoma	17535989	CNVD
Pheochromocytoma	17535989	CNVD
Prostate cancer	16705090	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Neuroblastoma	17533364	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
small cell lung cancer	20016488	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Basal cell lymphoma	21115979	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Chronic myeloid leukemia	21384125	CNVD
lymphocytic leukemia	21291569	CNVD
Prostate cancer	18632612	CNVD
Autism	22495311	CNVD
Neuroblastoma	18923191	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Non-small cell lung cancer	21385341	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Chordoma	21602918	CNVD
Lung cancer	18438408	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Multiple myeloma	16461302	CNVD
Glioblastoma multiforme	21138945	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Ovarian neoplasms	16753589	CNVD
Neuroblastoma	19287153	CNVD
Hepatocellular carcinoma	18929564	CNVD
Melanoma	17363583	CNVD
renal disease	17924346	CNVD
Uveal melanoma	20484589	CNVD
Multiple myeloma	16616336	CNVD
Glioblastoma multiforme	22286061	CNVD
Myelofibrosis	22110671	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Cancer	20164919	CNVD
Autism	20808228	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:288 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:10460000-10490200	Weak transcription	Psoas Muscle	Psoas
2	chr1:10460600-10481200	Strong transcription	H1 Cell Line	embryonic stem cell
3	chr1:10460800-10482000	Strong transcription	HUES48 Cell Line	embryonic stem cell
4	chr1:10460800-10482400	Strong transcription	Fetal Stomach	stomach
5	chr1:10460800-10483400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr1:10461000-10482000	Strong transcription	iPS-18 Cell Line	embryonic stem cell
7	chr1:10461200-10482000	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
8	chr1:10461200-10482000	Strong transcription	Fetal Muscle Leg	muscle
9	chr1:10461200-10490000	Weak transcription	Right Atrium	heart
10	chr1:10461400-10483000	Strong transcription	Cortex derived primary cultured neurospheres	brain
11	chr1:10461400-10483000	Strong transcription	Fetal Intestine Small	intestine
12	chr1:10461400-10483400	Strong transcription	Fetal Muscle Trunk	muscle
13	chr1:10461600-10481800	Strong transcription	iPS-20b Cell Line	embryonic stem cell
14	chr1:10461600-10482800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr1:10461800-10482000	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr1:10461800-10482000	Strong transcription	Dnd41	blood
17	chr1:10462000-10482000	Strong transcription	Fetal Intestine Large	intestine
18	chr1:10462000-10482200	Strong transcription	Brain Germinal Matrix	brain
19	chr1:10462000-10483000	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
20	chr1:10462200-10481600	Strong transcription	Liver	Liver
21	chr1:10462200-10481600	Strong transcription	Skeletal Muscle Male	skeletal muscle
22	chr1:10462200-10482000	Strong transcription	Sigmoid Colon	Sigmoid Colon
23	chr1:10462200-10483200	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
24	chr1:10462600-10482000	Strong transcription	Duodenum Mucosa	Duodenum
25	chr1:10462800-10481600	Strong transcription	Rectal Mucosa Donor 29	rectum
26	chr1:10462800-10481600	Strong transcription	GM12878-XiMat	blood
27	chr1:10462800-10482200	Strong transcription	Thymus	Thymus
28	chr1:10462800-10482600	Strong transcription	Brain Anterior Caudate	brain
29	chr1:10462800-10483400	Strong transcription	Fetal Brain Female	brain
30	chr1:10463000-10480800	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
31	chr1:10463000-10480800	Strong transcription	Left Ventricle	heart
32	chr1:10463000-10480800	Strong transcription	Skeletal Muscle Female	skeletal muscle
33	chr1:10463000-10481000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
34	chr1:10463000-10481000	Strong transcription	Brain Inferior Temporal Lobe	brain
35	chr1:10463000-10482000	Strong transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr1:10463000-10482200	Strong transcription	Fetal Thymus	thymus
37	chr1:10463200-10482000	Strong transcription	Brain Cingulate Gyrus	brain
38	chr1:10464200-10482000	Strong transcription	Spleen	Spleen
39	chr1:10464400-10481800	Strong transcription	HSMMtube	muscle
40	chr1:10464400-10482200	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
41	chr1:10464400-10482400	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
42	chr1:10464400-10482800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
43	chr1:10466000-10481800	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
44	chr1:10466200-10480800	Strong transcription	HepG2	liver
45	chr1:10466400-10481800	Strong transcription	Primary T cells from cord blood	blood
46	chr1:10468800-10489800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
47	chr1:10470400-10482000	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
48	chr1:10472000-10490000	Weak transcription	Stomach Mucosa	stomach
49	chr1:10473600-10488000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
50	chr1:10474200-10488000	Weak transcription	Pancreatic Islets	Pancreatic Islet

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