Variant report

Variant	esv1825811
Chromosome Location	chr1:210082206-210135806
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr1:210104726-210104737	K562	blood:	n/a	n/a
2	BACH1	chr1:210110958-210111334	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr1:210111563-210112084	H1-hESC	embryonic stem cell:	n/a	n/a
4	BATF	chr1:210110931-210111193	GM12878	blood:	n/a	n/a
5	BATF	chr1:210110933-210111244	GM12878	blood:	n/a	n/a
6	BCLAF1	chr1:210111028-210111270	GM12878	blood:	n/a	chr1:210111130-210111139
7	BRCA1	chr1:210111414-210111537	H1-hESC	embryonic stem cell:	n/a	n/a
8	CEBPB	chr1:210110630-210111234	H1-hESC	embryonic stem cell:	n/a	n/a
9	CEBPB	chr1:210128597-210128870	H1-hESC	embryonic stem cell:	n/a	n/a
10	CEBPB	chr1:210133056-210133371	K562	blood:	n/a	chr1:210133192-210133203
11	CEBPB	chr1:210128580-210128861	Hela-S3	cervix:	n/a	n/a
12	CEBPB	chr1:210133050-210133317	A549	lung:	n/a	chr1:210133192-210133203
13	CEBPB	chr1:210128550-210128871	HepG2	liver:	n/a	n/a
14	CEBPB	chr1:210128559-210128799	K562	blood:	n/a	n/a
15	CEBPB	chr1:210133064-210133342	HepG2	liver:	n/a	chr1:210133192-210133203
16	CEBPB	chr1:210128602-210128860	A549	lung:	n/a	n/a
17	CEBPB	chr1:210110490-210110509	A549	lung:	n/a	n/a
18	CEBPB	chr1:210098101-210098295	K562	blood:	n/a	n/a
19	CEBPB	chr1:210110914-210111251	IMR90	lung:	n/a	n/a
20	CEBPB	chr1:210133070-210133303	IMR90	lung:	n/a	chr1:210133192-210133203
21	CEBPB	chr1:210128526-210128969	A549	lung:	n/a	n/a
22	CEBPB	chr1:210111093-210111172	HepG2	liver:	n/a	n/a
23	CEBPB	chr1:210128567-210128897	K562	blood:	n/a	n/a
24	CEBPB	chr1:210128549-210128898	IMR90	lung:	n/a	n/a
25	CEBPD	chr1:210104436-210104967	K562	blood:	n/a	n/a
26	CEBPD	chr1:210104470-210104892	K562	blood:	n/a	n/a
27	CHD1	chr1:210110861-210112436	H1-hESC	embryonic stem cell:	n/a	chr1:210111320-210111330
28	CHD2	chr1:210111539-210111663	H1-hESC	embryonic stem cell:	n/a	n/a
29	CTCF	chr1:210111820-210111970	HCM	heart:	n/a	chr1:210111911-210111929 chr1:210111910-210111923 chr1:210111913-210111926
30	CTCF	chr1:210099540-210099690	BE2_C	brain:	n/a	n/a
31	CTCF	chr1:210111848-210112016	Fibrobl	skin:	n/a	chr1:210111911-210111929 chr1:210111910-210111923 chr1:210111913-210111926
32	CTCF	chr1:210111529-210111633	NHEK	skin:	n/a	n/a
33	CTCF	chr1:210111800-210111950	HCPEpiC	choroid plexus:	n/a	chr1:210111911-210111929 chr1:210111910-210111923 chr1:210111913-210111926
34	CTCF	chr1:210111776-210112001	H1-hESC	embryonic stem cell:	n/a	chr1:210111911-210111929 chr1:210111910-210111923 chr1:210111913-210111926
35	CTCF	chr1:210111820-210111970	AG04450	lung:	n/a	chr1:210111911-210111929 chr1:210111910-210111923 chr1:210111913-210111926
36	CTCF	chr1:210111900-210112050	HPAF	blood vessel:	n/a	chr1:210111911-210111929 chr1:210111910-210111923 chr1:210111913-210111926
37	CTCF	chr1:210111460-210111610	SK-N-SH_RA	brain:	n/a	n/a
38	CTCF	chr1:210111880-210112030	HMEC	breast:	n/a	chr1:210111911-210111929 chr1:210111910-210111923 chr1:210111913-210111926
39	CTCF	chr1:210111020-210111170	AG04450	lung:	n/a	n/a
40	CTCF	chr1:210111880-210112030	WERI-Rb-1	eye:	n/a	chr1:210111911-210111929 chr1:210111910-210111923 chr1:210111913-210111926
41	CTCF	chr1:210111880-210112030	SK-N-SH_RA	brain:	n/a	chr1:210111911-210111929 chr1:210111910-210111923 chr1:210111913-210111926
42	CTCF	chr1:210112080-210112230	AG04450	lung:	n/a	n/a
43	CTCF	chr1:210111860-210112010	HRPEpiC	eye:	n/a	chr1:210111911-210111929 chr1:210111910-210111923 chr1:210111913-210111926
44	CTCF	chr1:210111877-210111992	NHEK	skin:	n/a	chr1:210111911-210111929 chr1:210111910-210111923 chr1:210111913-210111926
45	CTCF	chr1:210111493-210111607	Fibrobl	skin:	n/a	n/a
46	CTCF	chr1:210101920-210102027	MCF-7	breast:	n/a	n/a
47	CTCF	chr1:210111860-210112010	BJ	skin:	n/a	chr1:210111911-210111929 chr1:210111910-210111923 chr1:210111913-210111926
48	CTCF	chr1:210111900-210112050	AG09319	gingival:	n/a	chr1:210111911-210111929 chr1:210111910-210111923 chr1:210111913-210111926
49	CTCF	chr1:210111940-210112090	HCFaa	heart:	n/a	n/a
50	CTCF	chr1:210111524-210111527	NHEK	skin:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:210111057-210111107	Hela-S3	cervix:	n/a
2	chr1:210110998-210111048	NB4	blood:	n/a
3	chr1:210111057-210111107	Hela-S3	cervix:	n/a
4	chr1:210110998-210111048	NB4	blood:	n/a
5	chr1:210109513-210109563	AoSMC	blood vessel:	n/a
6	chr1:210108326-210108376	AG04450	lung:	fetal
7	chr1:210115499-210115549	HIPEpiC	eye:	n/a
8	chr1:210113100-210113150	HepG2	liver:	n/a
9	chr1:210113100-210113150	H1-hESC	embryonic stem cell:	embryo
10	chr1:210109513-210109563	U87	brain:	n/a
11	chr1:210111057-210111107	AoSMC	blood vessel:	n/a
12	chr1:210108326-210108376	U87	brain:	n/a
13	chr1:210113100-210113150	GM19239	blood:	n/a
14	chr1:210111011-210111061	HRCEpiC	kidney:	n/a
15	chr1:210115499-210115549	HEEpiC	esophagus:	n/a
16	chr1:210108326-210108376	CMK	blood:	n/a
17	chr1:210115499-210115549	Hepatocyte	liver:	n/a
18	chr1:210115499-210115549	ECC-1	luminal epithelium:	n/a
19	chr1:210111028-210111078	HNPCEpiC	eye:	n/a
20	chr1:210111057-210111107	CMK	blood:	n/a
21	chr1:210112031-210112081	IMR90	lung:	fetal
22	chr1:210111011-210111061	HEK293	kidney:	embryo
23	chr1:210111011-210111061	HL-60	blood:	n/a
24	chr1:210113100-210113150	HEK293	kidney:	embryo
25	chr1:210113100-210113150	MCF10A-Er-Src	breast:	n/a
26	chr1:210108326-210108376	Hepatocyte	liver:	n/a
27	chr1:210111028-210111078	NB4	blood:	n/a
28	chr1:210111561-210111611	AG09319	gingival:	n/a
29	chr1:210111561-210111611	NT2-D1	testis:	n/a
30	chr1:210111162-210111212	NHDF-neo	bronchial:	n/a
31	chr1:210109513-210109563	LNCaP	prostate:	n/a
32	chr1:210111028-210111078	MCF-7	breast:	n/a
33	chr1:210115499-210115549	CMK	blood:	n/a
34	chr1:210111028-210111078	HRPEpiC	eye:	n/a
35	chr1:210113100-210113150	GM12892	blood:	n/a
36	chr1:210111028-210111078	H1-hESC	embryonic stem cell:	embryo
37	chr1:210111057-210111107	AG04450	lung:	fetal
38	chr1:210111057-210111107	HCT-116	colon:	n/a
39	chr1:210111672-210111722	MCF-7	breast:	n/a
40	chr1:210111403-210111453	NHDF-neo	bronchial:	n/a
41	chr1:210111672-210111722	NHBE	bronchial:	n/a
42	chr1:210111028-210111078	NT2-D1	testis:	n/a
43	chr1:210109513-210109563	PANC-1	pancreas:	n/a
44	chr1:210110998-210111048	RPTEC	kidney:	n/a
45	chr1:210115499-210115549	BE2_C	brain:	n/a
46	chr1:210111028-210111078	AG09309	skin:	n/a
47	chr1:210115499-210115549	HCM	heart:	n/a
48	chr1:210111011-210111061	RPTEC	kidney:	n/a
49	chr1:210113100-210113150	HEEpiC	esophagus:	n/a
50	chr1:210111162-210111212	BE2_C	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:210103690..210106151-chr1:210106770..210109170,2	K562	blood:
2	chr1:210101151..210102860-chr1:210546130..210547830,2	K562	blood:
3	chr1:210109695..210111724-chr1:210115043..210117369,2	K562	blood:
4	chr1:210000011..210002794-chr1:210097797..210100513,2	K562	blood:
5	chr1:210111478..210111978-chr11:236018..236738,2	K562	blood:
6	chr1:210101105..210102651-chr1:210546330..210548739,2	K562	blood:
7	chr1:210103690..210106151-chr1:210106770..210109170,2	K562	blood:
8	chr1:210077721..210079248-chr1:210084762..210086473,2	MCF-7	breast:
9	chr1:210099710..210101405-chr1:210104542..210107645,3	K562	blood:
10	chr1:210117640..210119739-chr1:210131346..210133429,2	K562	blood:
11	chr1:210110224..210112000-chr1:210114376..210116543,2	K562	blood:
12	chr1:210134246..210137088-chr1:210140873..210143040,2	K562	blood:
13	chr1:210117640..210119739-chr1:210131346..210133429,2	K562	blood:
14	chr1:210099710..210101405-chr1:210104542..210107645,3	K562	blood:
15	chr1:210129000..210131185-chr1:210545129..210547627,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-IRF6-1	chr1:210107873-210111294	NONHSAT009248

Variant related genes	Relation type
SYT14	TF binding region
SYT14	CpG island
ENSG00000185627	chromatin interactions
ENSG00000117597	chromatin interactions
ENSG00000200972	chromatin interactions
ENSG00000142082	chromatin interactions
ENSG00000143469	chromatin interactions

Extended variants
information (count: 1419 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:1419 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs542362165	chr1:210084823-210084824	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs561010655	chr1:210084830-210084831	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs58638851	chr1:210084880-210084881	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs546827385	chr1:210084971-210084972	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs117128985	chr1:210085037-210085038	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs532716366	chr1:210085106-210085107	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs550855326	chr1:210085107-210085108	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs11587397	chr1:210085120-210085121	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs150775656	chr1:210085181-210085182	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs529305437	chr1:210085451-210085452	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs72649918	chr1:210085587-210085588	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs569229621	chr1:210085600-210085601	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs78715764	chr1:210085640-210085641	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs555925215	chr1:210085666-210085667	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs534270527	chr1:210085824-210085825	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs1883309	chr1:210085870-210085871	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs1883310	chr1:210085977-210085978	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs149509399	chr1:210086246-210086247	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs189585073	chr1:210086252-210086253	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs572633865	chr1:210086253-210086254	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs182273504	chr1:210086310-210086311	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs9429827	chr1:210086341-210086342	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs546027955	chr1:210086348-210086349	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs550993665	chr1:210086400-210086401	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs371107184	chr1:210092800-210092801	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs562921713	chr1:210092841-210092842	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs530451747	chr1:210092884-210092885	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs11119365	chr1:210092916-210092917	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs12045009	chr1:210092938-210092939	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs35253623	chr1:210092962-210092963	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs151023548	chr1:210092963-210092964	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs527643449	chr1:210092967-210092968	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs12042489	chr1:210092986-210092987	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs140574560	chr1:210093001-210093002	ZNF genes & repeats Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs368139069	chr1:210093009-210093010	ZNF genes & repeats Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs12409613	chr1:210093031-210093032	ZNF genes & repeats Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs375684660	chr1:210093066-210093067	ZNF genes & repeats Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs59786763	chr1:210093088-210093089	ZNF genes & repeats Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs12041818	chr1:210093097-210093098	ZNF genes & repeats Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs12045067	chr1:210093106-210093107	ZNF genes & repeats Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs36074992	chr1:210093108-210093109	ZNF genes & repeats Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs375914677	chr1:210093109-210093110	ZNF genes & repeats Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs567272949	chr1:210093131-210093132	ZNF genes & repeats Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs61820371	chr1:210093133-210093134	ZNF genes & repeats Flanking Active TSS Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs372360304	chr1:210093159-210093160	ZNF genes & repeats Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs114905399	chr1:210093217-210093218	ZNF genes & repeats Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs558244374	chr1:210093224-210093225	ZNF genes & repeats Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs576561413	chr1:210093233-210093234	ZNF genes & repeats Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs543947693	chr1:210093248-210093249	ZNF genes & repeats Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs556762761	chr1:210093326-210093327	ZNF genes & repeats Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:90)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Autism	22495311	CNVD
Liposarcoma	21253554	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Rett syndrome	21593744	CNVD
Medulloblastoma	21979893	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	17443227	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
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
Acute lymphoblastic leukemia	21098271	CNVD
Neuroblastoma	21899760	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Non-small cell lung cancer	21385341	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Testicular germ cell tumor	18059402	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Breast cancer	21509527	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17393978	CNVD
Hepatocellular carcinoma	16750200	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Trisomy 5 syndrome	21098271	CNVD
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Chordoma	18071362	CNVD
Macular degeneration	22558131	CNVD
Alzheimer''s disease	21403675	CNVD
Multiple myeloma	16461302	CNVD
van der Woude syndrome	22470819	CNVD
van der Woude syndrome	20818247	CNVD
T-cell lymphomas	19863542	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	17060936	CNVD
Atypical hemolytic uremic syndrome	19861685	CNVD
Hepatocellular carcinoma	18803288	CNVD
Urothelial tumor	18831757	CNVD
Lung cancer	18438408	CNVD
Ovarian cancer	21720365	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Breast cancer	21611746	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:369 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:210084800-210085600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
2	chr1:210084800-210086000	Enhancers	HMEC	breast
3	chr1:210086200-210086400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr1:210092800-210093000	Enhancers	iPS-15b Cell Line	embryonic stem cell
5	chr1:210093000-210093400	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
6	chr1:210093000-210093600	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
7	chr1:210093000-210093600	Active TSS	K562	blood
8	chr1:210093400-210093600	Enhancers	iPS-15b Cell Line	embryonic stem cell
9	chr1:210097400-210100400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr1:210097600-210097800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
11	chr1:210097800-210098600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
12	chr1:210097800-210099200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
13	chr1:210098600-210099400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
14	chr1:210098800-210100200	Enhancers	Hela-S3	cervix
15	chr1:210098800-210101000	Enhancers	NH-A	brain
16	chr1:210099000-210099200	Enhancers	Muscle Satellite Cultured Cells	--
17	chr1:210099000-210100400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
18	chr1:210099000-210100400	Enhancers	HMEC	breast
19	chr1:210099000-210100400	Enhancers	NHEK	skin
20	chr1:210099200-210099400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr1:210099200-210099400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
22	chr1:210099200-210099400	Flanking Active TSS	HSMMtube	muscle
23	chr1:210099200-210099600	Flanking Active TSS	Muscle Satellite Cultured Cells	--
24	chr1:210099200-210100200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
25	chr1:210099200-210100200	Enhancers	Pancreatic Islets	Pancreatic Islet
26	chr1:210099200-210100200	Enhancers	Osteobl	bone
27	chr1:210099200-210100400	Enhancers	HSMM	muscle
28	chr1:210099200-210100600	Enhancers	Cortex derived primary cultured neurospheres	brain
29	chr1:210099200-210101000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
30	chr1:210099200-210101200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
31	chr1:210099400-210099600	Enhancers	HUES64 Cell Line	embryonic stem cell
32	chr1:210099400-210099600	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
33	chr1:210099400-210099800	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
34	chr1:210099400-210100000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
35	chr1:210099400-210100200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
36	chr1:210099400-210100200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
37	chr1:210099400-210100800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
38	chr1:210099400-210101000	Enhancers	Brain Germinal Matrix	brain
39	chr1:210099400-210101200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
40	chr1:210099400-210101200	Enhancers	HSMMtube	muscle
41	chr1:210099600-210100200	Weak transcription	HUES64 Cell Line	embryonic stem cell
42	chr1:210099600-210101200	Enhancers	Muscle Satellite Cultured Cells	--
43	chr1:210099800-210101200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
44	chr1:210100200-210101200	Enhancers	HUES64 Cell Line	embryonic stem cell
45	chr1:210100200-210107800	Weak transcription	Pancreatic Islets	Pancreatic Islet
46	chr1:210100400-210103000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
47	chr1:210103000-210103200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
48	chr1:210104200-210105400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
49	chr1:210104400-210105400	Enhancers	Primary hematopoietic stem cells	blood
50	chr1:210104400-210105600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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