Variant report

Variant	nsv872833
Chromosome Location	chr1:193681625-193774083
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	ATF2	chr1:193710341-193710777	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr1:193712976-193713031	K562	blood:	n/a	n/a
3	BCL11A	chr1:193710422-193710666	H1-hESC	embryonic stem cell:	n/a	n/a
4	BHLHE40	chr1:193722598-193722750	HepG2	liver:	n/a	n/a
5	BRCA1	chr1:193698698-193699470	Hela-S3	cervix:	n/a	chr1:193699005-193699012
6	CEBPB	chr1:193699089-193699516	A549	lung:	n/a	chr1:193699268-193699279
7	CEBPB	chr1:193716865-193717019	Hela-S3	cervix:	n/a	n/a
8	CEBPB	chr1:193750519-193750693	A549	lung:	n/a	chr1:193750599-193750612 chr1:193750599-193750610 chr1:193750599-193750610 chr1:193750599-193750612 chr1:193750599-193750612
9	CEBPB	chr1:193716748-193717098	IMR90	lung:	n/a	n/a
10	CEBPB	chr1:193699108-193699363	H1-hESC	embryonic stem cell:	n/a	chr1:193699268-193699279
11	CEBPB	chr1:193703282-193703531	HepG2	liver:	n/a	chr1:193703393-193703404
12	CEBPB	chr1:193764029-193764448	A549	lung:	n/a	chr1:193764165-193764178 chr1:193764167-193764176 chr1:193764165-193764176 chr1:193764167-193764176 chr1:193764165-193764178 chr1:193764167-193764178 chr1:193764167-193764176 chr1:193764167-193764176
13	CEBPB	chr1:193699110-193699457	HepG2	liver:	n/a	chr1:193699268-193699279
14	CEBPB	chr1:193764019-193764408	HepG2	liver:	n/a	chr1:193764165-193764178 chr1:193764167-193764176 chr1:193764165-193764176 chr1:193764167-193764176 chr1:193764165-193764178 chr1:193764167-193764178 chr1:193764167-193764176 chr1:193764167-193764176
15	CEBPB	chr1:193695894-193696197	IMR90	lung:	n/a	n/a
16	CEBPB	chr1:193698986-193699504	IMR90	lung:	n/a	chr1:193699268-193699279
17	CEBPB	chr1:193699094-193699474	A549	lung:	n/a	chr1:193699268-193699279
18	CEBPB	chr1:193740358-193740365	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr1:193698681-193699641	Hela-S3	cervix:	n/a	chr1:193699268-193699279
20	CEBPB	chr1:193699183-193699433	MCF-7	breast:	n/a	chr1:193699268-193699279
21	CEBPB	chr1:193764016-193764349	IMR90	lung:	n/a	chr1:193764165-193764178 chr1:193764167-193764176 chr1:193764165-193764176 chr1:193764167-193764176 chr1:193764165-193764178 chr1:193764167-193764178 chr1:193764167-193764176 chr1:193764167-193764176
22	CEBPB	chr1:193750535-193750643	K562	blood:	n/a	chr1:193750599-193750612 chr1:193750599-193750610 chr1:193750599-193750610 chr1:193750599-193750612 chr1:193750599-193750612
23	CEBPB	chr1:193699029-193699628	A549	lung:	n/a	chr1:193699268-193699279
24	CTCF	chr1:193724280-193724430	Caco-2	colon:	n/a	chr1:193724359-193724372 chr1:193724357-193724375 chr1:193724352-193724373
25	CTCF	chr1:193724300-193724450	AoAF	blood vessel:	n/a	chr1:193724359-193724372 chr1:193724357-193724375 chr1:193724352-193724373
26	CTCF	chr1:193763410-193763542	Pancreas_OC	pancreas:	n/a	n/a
27	CTCF	chr1:193724098-193724481	MCF-7	breast:	n/a	chr1:193724359-193724372 chr1:193724357-193724375 chr1:193724352-193724373
28	CTCF	chr1:193756262-193756375	Hela-S3	cervix:	n/a	n/a
29	CTCF	chr1:193724280-193724430	GM12871	blood:	n/a	chr1:193724359-193724372 chr1:193724357-193724375 chr1:193724352-193724373
30	CTCF	chr1:193735600-193735750	WERI-Rb-1	eye:	n/a	n/a
31	CTCF	chr1:193756200-193756350	HCPEpiC	choroid plexus:	n/a	n/a
32	CTCF	chr1:193756100-193756250	AG04450	lung:	n/a	n/a
33	CTCF	chr1:193735540-193735690	MCF-7	breast:	n/a	n/a
34	CTCF	chr1:193735580-193735730	HEEpiC	esophagus:	n/a	n/a
35	CTCF	chr1:193746216-193746296	Kidney_OC	kidney:	n/a	n/a
36	CTCF	chr1:193724340-193724490	HMEC	breast:	n/a	chr1:193724359-193724372 chr1:193724357-193724375 chr1:193724352-193724373
37	CTCF	chr1:193724280-193724430	HCPEpiC	choroid plexus:	n/a	chr1:193724359-193724372 chr1:193724357-193724375 chr1:193724352-193724373
38	CTCF	chr1:193724260-193724410	HPF	lung:	n/a	chr1:193724359-193724372 chr1:193724357-193724375 chr1:193724352-193724373
39	CTCF	chr1:193724249-193724467	Spleen_OC	spleen:	n/a	chr1:193724359-193724372 chr1:193724357-193724375 chr1:193724352-193724373
40	CTCF	chr1:193756280-193756430	Caco-2	colon:	n/a	n/a
41	CTCF	chr1:193756160-193756310	WERI-Rb-1	eye:	n/a	n/a
42	CTCF	chr1:193763380-193763530	HBMEC	blood vessel:	n/a	n/a
43	CTCF	chr1:193724294-193724391	Gliobla	brain:	n/a	chr1:193724359-193724372 chr1:193724357-193724375 chr1:193724352-193724373
44	CTCF	chr1:193724280-193724430	NHEK	skin:	n/a	chr1:193724359-193724372 chr1:193724357-193724375 chr1:193724352-193724373
45	CTCF	chr1:193756180-193756330	RPTEC	kidney:	n/a	n/a
46	CTCF	chr1:193724260-193724410	MCF-7	breast:	n/a	chr1:193724359-193724372 chr1:193724357-193724375 chr1:193724352-193724373
47	CTCF	chr1:193724320-193724470	GM12864	blood:	n/a	chr1:193724359-193724372 chr1:193724357-193724375 chr1:193724352-193724373
48	CTCF	chr1:193724260-193724410	SAEC	small airway:	n/a	chr1:193724359-193724372 chr1:193724357-193724375 chr1:193724352-193724373
49	CTCF	chr1:193724280-193724430	GM12872	blood:	n/a	chr1:193724359-193724372 chr1:193724357-193724375 chr1:193724352-193724373
50	CTCF	chr1:193724240-193724390	HVMF	connective:	n/a	chr1:193724359-193724372 chr1:193724357-193724375 chr1:193724352-193724373

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:193710042-193710092	Caco-2	colon:	n/a
2	chr1:193722865-193722915	Hepatocyte	liver:	n/a
3	chr1:193722865-193722915	SK-N-MC	brain:	n/a
4	chr1:193722865-193722915	H1-hESC	embryonic stem cell:	embryo
5	chr1:193710042-193710092	SK-N-SH_RA	brain:	n/a
6	chr1:193722865-193722915	HEK293	kidney:	embryo
7	chr1:193722865-193722915	IMR90	lung:	fetal
8	chr1:193710042-193710092	AG09319	gingival:	n/a
9	chr1:193722865-193722915	HNPCEpiC	eye:	n/a
10	chr1:193722865-193722915	A549	lung:	n/a
11	chr1:193722865-193722915	Jurkat	blood:	n/a
12	chr1:193710042-193710092	GM12891	blood:	n/a
13	chr1:193710042-193710092	HUVEC	blood vessel:	n/a
14	chr1:193722865-193722915	AG04449	skin:	fetal
15	chr1:193722865-193722915	AG09309	skin:	n/a
16	chr1:193710042-193710092	GM12892	blood:	n/a
17	chr1:193722865-193722915	HUVEC	blood vessel:	n/a
18	chr1:193710042-193710092	GM06990	blood:	n/a
19	chr1:193710042-193710092	CMK	blood:	n/a
20	chr1:193710042-193710092	NHDF-neo	bronchial:	n/a
21	chr1:193710042-193710092	GM19239	blood:	n/a
22	chr1:193722865-193722915	PANC-1	pancreas:	n/a
23	chr1:193722865-193722915	HCPEpiC	choroid plexus:	n/a
24	chr1:193710042-193710092	Hela-S3	cervix:	n/a
25	chr1:193710042-193710092	SK-N-MC	brain:	n/a
26	chr1:193710042-193710092	HCF	heart:	n/a
27	chr1:193722865-193722915	BJ	skin:	n/a
28	chr1:193710042-193710092	AoSMC	blood vessel:	n/a
29	chr1:193722865-193722915	U87	brain:	n/a
30	chr1:193710042-193710092	HL-60	blood:	n/a
31	chr1:193710042-193710092	RPTEC	kidney:	n/a
32	chr1:193722865-193722915	ovcar-3	ovarian:	n/a
33	chr1:193710042-193710092	ProgFib	skin:	n/a
34	chr1:193722865-193722915	CMK	blood:	n/a
35	chr1:193710042-193710092	HRPEpiC	eye:	n/a
36	chr1:193710042-193710092	SK-N-SH	brain:	n/a
37	chr1:193710042-193710092	U87	brain:	n/a
38	chr1:193710042-193710092	HPAEpiC	pulmonary alveolar:	n/a
39	chr1:193710042-193710092	ECC-1	luminal epithelium:	n/a
40	chr1:193710042-193710092	ovcar-3	ovarian:	n/a
41	chr1:193722865-193722915	HPAEpiC	pulmonary alveolar:	n/a
42	chr1:193722865-193722915	HMEC	breast:	n/a
43	chr1:193722865-193722915	RPTEC	kidney:	n/a
44	chr1:193722865-193722915	BE2_C	brain:	n/a
45	chr1:193722865-193722915	AG04450	lung:	fetal
46	chr1:193710042-193710092	AG04449	skin:	fetal
47	chr1:193710042-193710092	A549	lung:	n/a
48	chr1:193710042-193710092	HEK293	kidney:	embryo
49	chr1:193710042-193710092	NHBE	bronchial:	n/a
50	chr1:193722865-193722915	HCM	heart:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:193715834..193718393-chr1:193725574..193727798,2	K562	blood:
2	chr1:193678450..193681158-chr1:193682285..193685229,2	K562	blood:
3	chr1:193728373..193730698-chr1:193736583..193739356,2	K562	blood:
4	chr1:193734313..193736355-chr1:193736436..193738491,2	K562	blood:
5	chr1:193728373..193730698-chr1:193736583..193739356,2	K562	blood:
6	chr1:193734313..193736355-chr1:193736436..193738491,2	K562	blood:
7	chr1:193375633..193376607-chr1:193723998..193724709,3	MCF-7	breast:
8	chr1:193705634..193708384-chr1:193710266..193712838,2	MCF-7	breast:
9	chr1:193576779..193577361-chr1:193723828..193724666,2	MCF-7	breast:
10	chr1:193723167..193725389-chr1:193725651..193727623,2	MCF-7	breast:
11	chr1:193681603..193683732-chr11:100996114..100998464,2	MCF-7	breast:
12	chr1:193705634..193708384-chr1:193710266..193712838,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CDC73-2	chr1:193694731-193694815	ENSG00000226640.2
2	lnc-CDC73-2	chr1:193694731-193694815	XLOC_000509
3	lnc-B3GALT2-3	chr1:193725945-193726397	NONHSAT008575
4	lnc-CDC73-2	chr1:193695962-193696313	XLOC_000509
5	lnc-CDC73-2	chr1:193695962-193696165	ENSG00000226640.2

Variant related genes	Relation type
RPL23AP22	TF binding region
ENSG00000252241	TF binding region
RPL23AP22	CpG island
ENSG00000252241	CpG island
ENSG00000237213	chromatin interactions

Extended variants
information (count: 1919 )
Associated
traits (count: 94 )

Variant overlapped rSNPs/rCNVs (count:1919 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2149178	chr1:193681625-193681626	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs143234870	chr1:193681643-193681644	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs561352893	chr1:193681657-193681658	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs574859132	chr1:193681672-193681673	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs540538015	chr1:193681680-193681681	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs560445792	chr1:193681682-193681683	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs532436523	chr1:193681690-193681691	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs552391711	chr1:193681691-193681692	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs549768291	chr1:193681695-193681696	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs531469396	chr1:193681700-193681701	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs547942429	chr1:193681721-193681722	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs147500177	chr1:193681771-193681772	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs377276964	chr1:193681841-193681842	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs533146678	chr1:193681871-193681872	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs546980588	chr1:193681885-193681886	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs566871577	chr1:193681956-193681957	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs538942756	chr1:193681963-193681964	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs373467696	chr1:193684614-193684615	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs565719143	chr1:193684634-193684635	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs10921415	chr1:193684639-193684640	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs7541925	chr1:193684654-193684655	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs551622129	chr1:193684667-193684668	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs571354359	chr1:193684669-193684670	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs12408312	chr1:193684673-193684674	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs184621046	chr1:193684675-193684676	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs567414539	chr1:193684676-193684677	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs536331523	chr1:193684692-193684693	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs553020005	chr1:193684705-193684706	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs17376854	chr1:193684728-193684729	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs541364650	chr1:193684731-193684732	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs558391007	chr1:193684735-193684736	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs12034223	chr1:193684737-193684738	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs544043794	chr1:193684747-193684748	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs563522078	chr1:193684755-193684756	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs17376861	chr1:193684770-193684771	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs561483193	chr1:193684777-193684778	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs189945369	chr1:193684797-193684798	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs541308535	chr1:193684802-193684803	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs551394600	chr1:193684819-193684820	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs367564941	chr1:193684825-193684826	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs560492020	chr1:193684833-193684834	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs530710923	chr1:193684880-193684881	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs17304880	chr1:193684886-193684887	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs371325731	chr1:193684923-193684924	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs7552269	chr1:193684940-193684941	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs10709208	chr1:193684951-193684952	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs535555379	chr1:193694614-193694615	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs568222799	chr1:193694654-193694655	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs184069536	chr1:193694680-193694681	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs528404940	chr1:193694689-193694690	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:94)

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
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Carcinoma ex pleomorphic adenoma	18828159	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
Ovarian neoplasms	16753589	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
Hepatocellular carcinoma	18803288	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
Lung cancer	18438408	CNVD
Metanephric adenoma	20802469	CNVD
Melanoma	20688739	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21611746	CNVD
primary effusion lymphomas	17116491	CNVD
Breast cancer	17393978	CNVD
Hepatocellular carcinoma	16750200	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Non-small cell lung cancer	19010865	CNVD
Mental retardation	17847001	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Trisomy 5 syndrome	21098271	CNVD
Glioblastoma multiforme	22286061	CNVD
Urothelial carcinoma	21177765	CNVD
Lung adenocarcinoma	17086460	CNVD
Lung cancer	17086460	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16272173	CNVD
Mental retardation	21062444	CNVD
Liver carcinoma	19366792	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Pancreatic cancer	17952125	CNVD
T-cell lymphomas	22341440	CNVD

Chromatin state (count:137 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:193681600-193682000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr1:193684600-193685000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr1:193694600-193695000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
4	chr1:193695000-193697600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
5	chr1:193695800-193697800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
6	chr1:193696000-193696200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
7	chr1:193696400-193697600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr1:193696600-193697600	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
9	chr1:193696800-193697000	Bivalent Enhancer	H9 Cell Line	embryonic stem cell
10	chr1:193696800-193697200	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
11	chr1:193696800-193697200	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
12	chr1:193696800-193697600	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
13	chr1:193697000-193697400	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
14	chr1:193697600-193697800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
15	chr1:193698400-193698600	Enhancers	A549	lung
16	chr1:193698600-193698800	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
17	chr1:193698600-193699000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
18	chr1:193698600-193699400	Enhancers	Fetal Heart	heart
19	chr1:193698600-193699600	Flanking Active TSS	A549	lung
20	chr1:193698600-193700400	Enhancers	Hela-S3	cervix
21	chr1:193704600-193705200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
22	chr1:193705800-193707000	Enhancers	Fetal Heart	heart
23	chr1:193707400-193707600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
24	chr1:193707600-193707800	Enhancers	iPS-15b Cell Line	embryonic stem cell
25	chr1:193707600-193714800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
26	chr1:193708400-193709400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
27	chr1:193709000-193710200	Enhancers	HUES48 Cell Line	embryonic stem cell
28	chr1:193709400-193709800	Enhancers	iPS-15b Cell Line	embryonic stem cell
29	chr1:193709600-193710600	Enhancers	HUES64 Cell Line	embryonic stem cell
30	chr1:193709800-193710200	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
31	chr1:193709800-193710200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
32	chr1:193709800-193710600	Enhancers	HUES6 Cell Line	embryonic stem cell
33	chr1:193709800-193710600	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
34	chr1:193709800-193710800	Enhancers	ES-I3 Cell Line	embryonic stem cell
35	chr1:193710000-193710200	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
36	chr1:193710200-193710400	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
37	chr1:193710200-193710800	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
38	chr1:193710200-193711000	Enhancers	iPS-15b Cell Line	embryonic stem cell
39	chr1:193710400-193710600	Enhancers	HUES48 Cell Line	embryonic stem cell
40	chr1:193710600-193710800	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
41	chr1:193710600-193710800	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
42	chr1:193710600-193711200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
43	chr1:193710800-193711000	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
44	chr1:193712800-193713000	Enhancers	iPS-15b Cell Line	embryonic stem cell
45	chr1:193712800-193713400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
46	chr1:193712800-193713600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
47	chr1:193714800-193715000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
48	chr1:193715000-193715400	Enhancers	Fetal Heart	heart
49	chr1:193715200-193715400	Enhancers	iPS-15b Cell Line	embryonic stem cell
50	chr1:193722200-193723200	Enhancers	iPS-15b Cell Line	embryonic stem cell

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