Variant report

Variant	nsv830692
Chromosome Location	chr1:97501492-97625153
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:949)
CpG islands
(count:368)
Chromatin interactive
region (count:15)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:949 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:97529087-97529414	HepG2	liver:	n/a	n/a
2	ATF2	chr1:97624780-97625302	GM12878	blood:	n/a	n/a
3	ATF2	chr1:97624749-97625430	GM12878	blood:	n/a	n/a
4	ATF3	chr1:97604285-97604473	GM12878	blood:	n/a	chr1:97604459-97604468
5	BACH1	chr1:97585502-97585503	H1-hESC	embryonic stem cell:	n/a	n/a
6	BATF	chr1:97512272-97512746	GM12878	blood:	n/a	n/a
7	BATF	chr1:97610097-97610342	GM12878	blood:	n/a	chr1:97610243-97610254
8	BCL11A	chr1:97624953-97625272	GM12878	blood:	n/a	n/a
9	BCL3	chr1:97559293-97560187	A549	lung:	n/a	n/a
10	BCL3	chr1:97624926-97625264	GM12878	blood:	n/a	n/a
11	BCLAF1	chr1:97624828-97625336	GM12878	blood:	n/a	n/a
12	BHLHE40	chr1:97610180-97610183	GM12878	blood:	n/a	n/a
13	BHLHE40	chr1:97625001-97625209	GM12878	blood:	n/a	n/a
14	BHLHE40	chr1:97516201-97516207	GM12878	blood:	n/a	n/a
15	BHLHE40	chr1:97558182-97558222	GM12878	blood:	n/a	n/a
16	BRCA1	chr1:97559137-97560305	Hela-S3	cervix:	n/a	n/a
17	BRCA1	chr1:97616168-97616258	GM12878	blood:	n/a	n/a
18	CBX3	chr1:97522243-97522501	K562	blood:	n/a	n/a
19	CCNT2	chr1:97615260-97615460	K562	blood:	n/a	n/a
20	CEBPB	chr1:97529100-97529386	HepG2	liver:	n/a	n/a
21	CEBPB	chr1:97559273-97560284	A549	lung:	n/a	n/a
22	CEBPB	chr1:97589419-97589771	A549	lung:	n/a	chr1:97589683-97589700
23	CEBPB	chr1:97529176-97529393	A549	lung:	n/a	n/a
24	CEBPB	chr1:97624822-97625339	GM12878	blood:	n/a	n/a
25	CEBPB	chr1:97613727-97613917	HepG2	liver:	n/a	chr1:97613848-97613859
26	CEBPB	chr1:97529142-97529502	MCF-7	breast:	n/a	n/a
27	CEBPB	chr1:97517418-97517740	HepG2	liver:	n/a	chr1:97517556-97517567
28	CEBPB	chr1:97529031-97529500	HepG2	liver:	n/a	n/a
29	CEBPB	chr1:97516000-97516412	IMR90	lung:	n/a	n/a
30	CEBPB	chr1:97580659-97580914	IMR90	lung:	n/a	n/a
31	CEBPB	chr1:97580659-97580971	A549	lung:	n/a	n/a
32	CEBPB	chr1:97517447-97517636	K562	blood:	n/a	chr1:97517556-97517567
33	CEBPB	chr1:97565186-97565478	HepG2	liver:	n/a	chr1:97565332-97565343
34	CEBPB	chr1:97517388-97517745	IMR90	lung:	n/a	chr1:97517556-97517567
35	CEBPB	chr1:97516070-97516425	Hela-S3	cervix:	n/a	n/a
36	CEBPB	chr1:97609115-97609393	A549	lung:	n/a	chr1:97609201-97609212
37	CEBPB	chr1:97517405-97517715	Hela-S3	cervix:	n/a	chr1:97517556-97517567
38	CEBPB	chr1:97588145-97588304	A549	lung:	n/a	n/a
39	CEBPB	chr1:97559221-97560300	Hela-S3	cervix:	n/a	n/a
40	CEBPB	chr1:97615271-97615496	HepG2	liver:	n/a	chr1:97615388-97615399
41	CEBPB	chr1:97517471-97517657	H1-hESC	embryonic stem cell:	n/a	chr1:97517556-97517567
42	CEBPB	chr1:97559127-97560352	A549	lung:	n/a	n/a
43	CEBPB	chr1:97609090-97609442	Hela-S3	cervix:	n/a	chr1:97609201-97609212
44	CEBPB	chr1:97559909-97560247	A549	lung:	n/a	n/a
45	CEBPB	chr1:97589512-97589673	IMR90	lung:	n/a	n/a
46	CEBPB	chr1:97516098-97516416	H1-hESC	embryonic stem cell:	n/a	n/a
47	CEBPB	chr1:97559229-97560314	IMR90	lung:	n/a	n/a
48	CEBPB	chr1:97529051-97529411	MCF-7	breast:	n/a	n/a
49	CEBPB	chr1:97529158-97529427	HepG2	liver:	n/a	n/a
50	CEBPB	chr1:97517386-97517667	A549	lung:	n/a	chr1:97517556-97517567

(count:368 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:97565426-97565476	IMR90	lung:	fetal
2	chr1:97584888-97584938	MCF10A-Er-Src	breast:	n/a
3	chr1:97565426-97565476	IMR90	lung:	fetal
4	chr1:97584888-97584938	MCF10A-Er-Src	breast:	n/a
5	chr1:97604182-97604232	HRE	kidney:	n/a
6	chr1:97604182-97604232	HNPCEpiC	eye:	n/a
7	chr1:97542201-97542251	IMR90	lung:	fetal
8	chr1:97604182-97604232	AG10803	skin:	n/a
9	chr1:97542201-97542251	SK-N-MC	brain:	n/a
10	chr1:97584888-97584938	HAEpiC	amniotic membrane:	n/a
11	chr1:97604182-97604232	Jurkat	blood:	n/a
12	chr1:97610703-97610753	HL-60	blood:	n/a
13	chr1:97565426-97565476	NB4	blood:	n/a
14	chr1:97610703-97610753	SK-N-MC	brain:	n/a
15	chr1:97542201-97542251	SKMC	muscle:	n/a
16	chr1:97559808-97559858	MCF10A-Er-Src	breast:	n/a
17	chr1:97584888-97584938	HMEC	breast:	n/a
18	chr1:97559808-97559858	NHBE	bronchial:	n/a
19	chr1:97584888-97584938	HepG2	liver:	n/a
20	chr1:97565426-97565476	ECC-1	luminal epithelium:	n/a
21	chr1:97559808-97559858	HMEC	breast:	n/a
22	chr1:97610703-97610753	HPAEpiC	pulmonary alveolar:	n/a
23	chr1:97559808-97559858	A549	lung:	n/a
24	chr1:97559808-97559858	HRE	kidney:	n/a
25	chr1:97584888-97584938	AG09319	gingival:	n/a
26	chr1:97542201-97542251	RPTEC	kidney:	n/a
27	chr1:97604182-97604232	AG04449	skin:	fetal
28	chr1:97542201-97542251	HRCEpiC	kidney:	n/a
29	chr1:97565426-97565476	RPTEC	kidney:	n/a
30	chr1:97610703-97610753	SKMC	muscle:	n/a
31	chr1:97559808-97559858	K562	blood:	n/a
32	chr1:97584888-97584938	Hepatocyte	liver:	n/a
33	chr1:97542201-97542251	HEK293	kidney:	embryo
34	chr1:97559808-97559858	NHDF-neo	bronchial:	n/a
35	chr1:97604182-97604232	A549	lung:	n/a
36	chr1:97542201-97542251	AG09309	skin:	n/a
37	chr1:97604182-97604232	PrEC	prostate:	n/a
38	chr1:97565426-97565476	ovcar-3	ovarian:	n/a
39	chr1:97584888-97584938	HUVEC	blood vessel:	n/a
40	chr1:97584888-97584938	AG10803	skin:	n/a
41	chr1:97610703-97610753	Caco-2	colon:	n/a
42	chr1:97559808-97559858	GM12891	blood:	n/a
43	chr1:97604182-97604232	HIPEpiC	eye:	n/a
44	chr1:97584888-97584938	HCPEpiC	choroid plexus:	n/a
45	chr1:97604182-97604232	BJ	skin:	n/a
46	chr1:97542201-97542251	HMEC	breast:	n/a
47	chr1:97559808-97559858	NT2-D1	testis:	n/a
48	chr1:97565426-97565476	HAEpiC	amniotic membrane:	n/a
49	chr1:97565426-97565476	AG04450	lung:	fetal
50	chr1:97610703-97610753	HAEpiC	amniotic membrane:	n/a

(count:15 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:97603745..97604533-chr1:98286034..98286590,2	MCF-7	breast:
2	chr1:97569264..97571066-chr1:97574080..97575700,2	K562	blood:
3	chr1:97563525..97565032-chr1:97567677..97569831,2	MCF-7	breast:
4	chr1:97540562..97542621-chr1:97547174..97549970,2	MCF-7	breast:
5	chr1:97540562..97542621-chr1:97547174..97549970,2	MCF-7	breast:
6	chr1:97563525..97565032-chr1:97567677..97569831,2	MCF-7	breast:
7	chr1:97583499..97585918-chr1:97586058..97587654,2	K562	blood:
8	chr1:96628387..96630261-chr1:97558478..97560909,2	MCF-7	breast:
9	chr1:97603898..97604544-chr1:98516387..98516952,2	MCF-7	breast:
10	chr1:97603769..97604477-chr1:97990784..97991664,2	MCF-7	breast:
11	chr1:97432013..97432796-chr1:97515726..97516662,5	MCF-7	breast:
12	chr1:97516184..97517096-chr1:98516693..98517248,2	MCF-7	breast:
13	chr1:97515527..97518087-chr1:97560451..97562867,2	MCF-7	breast:
14	chr1:97569264..97571066-chr1:97574080..97575700,2	K562	blood:
15	chr1:97583499..97585918-chr1:97586058..97587654,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PTBP2-2	chr1:97561479-97561542	ENSG00000232878.1

No data

Variant related genes	Relation type
DPYD-AS1	TF binding region
DPYD-AS1	CpG island
ENSG00000232878	chromatin interactions

Extended variants
information (count: 4269 )
Associated
traits (count: 105 )

Variant overlapped rSNPs/rCNVs (count:4269 , 50 per page) page: 1 2 3 4 5 6 7 ... 86

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs556350074	chr1:97505834-97505835	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs181172532	chr1:97505901-97505902	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs552144228	chr1:97505907-97505908	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs142553957	chr1:97505912-97505913	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs185381821	chr1:97505945-97505946	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs576627951	chr1:97505963-97505964	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs539353313	chr1:97505997-97505998	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs558880774	chr1:97506001-97506002	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs534423119	chr1:97506028-97506029	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs572639855	chr1:97506048-97506049	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs188135548	chr1:97506099-97506100	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs370426186	chr1:97506138-97506139	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs150232627	chr1:97506170-97506171	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs575005925	chr1:97506217-97506218	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs369696682	chr1:97506251-97506252	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs543803141	chr1:97506287-97506288	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs563732796	chr1:97506293-97506294	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs567765604	chr1:97506294-97506295	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs7528151	chr1:97506344-97506345	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs536215189	chr1:97506345-97506346	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs527445394	chr1:97506380-97506381	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs577217356	chr1:97506453-97506454	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs138465263	chr1:97506461-97506462	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs181925856	chr1:97506462-97506463	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs76228359	chr1:97506471-97506472	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs549350965	chr1:97506482-97506483	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs149281397	chr1:97506573-97506574	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs369039322	chr1:97506603-97506604	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs143494761	chr1:97506604-97506605	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs535251815	chr1:97506665-97506666	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs572651592	chr1:97506703-97506704	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs113752579	chr1:97506721-97506722	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs535200563	chr1:97506724-97506725	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs555214346	chr1:97506767-97506768	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs186424606	chr1:97506770-97506771	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs543958911	chr1:97506811-97506812	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs12126417	chr1:97506812-97506813	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs183353139	chr1:97506880-97506881	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs545890428	chr1:97506909-97506910	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs377009071	chr1:97506915-97506916	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs565142006	chr1:97506920-97506921	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs371396133	chr1:97506929-97506930	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs137897986	chr1:97506963-97506964	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs373831015	chr1:97506988-97506989	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs547157071	chr1:97507005-97507006	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs186675605	chr1:97507007-97507008	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs373748163	chr1:97507037-97507038	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs376981997	chr1:97507075-97507076	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs549895714	chr1:97507095-97507096	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs142335431	chr1:97507097-97507098	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:105)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Coronary Disease	20032323	CNVD
Prostate cancer	21965145	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Stargardt''s disease	17277736	CNVD
Neuroblastoma	17897457	CNVD
Uveal melanoma	21693616	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	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
Papillary thyroid carcinoma	21436994	CNVD
Neuroblastoma	17535989	CNVD
Pheochromocytoma	17535989	CNVD
Prostate cancer	16705090	CNVD
Astrocytoma	17934521	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Gastrointestinal stromal cancer	19259404	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
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21385341	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Chordoma	21602918	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Melanoma	18172304	CNVD
Multiple myeloma	16461302	CNVD
Cancer	21129771	CNVD
Autosomal dominant nocturnal frontal lobe epilepsy	18472482	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thrombocytopenia-absent radius syndrome	21933853	CNVD
Psychiatric disorder	22848183	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	20409316	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Medulloblastoma	21979893	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Rett syndrome	21593744	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
Ovarian cancer	21720365	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Ewing''s sarcoma	17952124	CNVD
Cancer	22429812	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	17133270	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Esophageal adenocarcinoma	18820669	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Glioblastoma multiforme	21922591	CNVD
Autism	17483303	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Myelofibrosis	22110671	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Intestinal disease	21956041	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Gastric cancer	16891809	CNVD
Schizophrenia	17879154	CNVD
Mental retardation	17124404	CNVD
Intestinal disease	17828263	CNVD
Malignant melanoma	17260012	CNVD
lymphocytic leukemia	21291569	CNVD
Pancreatic cancer	17952125	CNVD
Cancer	20803296	CNVD
Colorectal cancer	20653680	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:97505800-97506000	Enhancers	Osteobl	bone
2	chr1:97506000-97507600	Weak transcription	Osteobl	bone
3	chr1:97506600-97507400	Enhancers	Muscle Satellite Cultured Cells	--
4	chr1:97507000-97507200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
5	chr1:97507200-97507400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
6	chr1:97507200-97508800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
7	chr1:97507600-97507800	Enhancers	Osteobl	bone
8	chr1:97507800-97508000	Enhancers	NHDF-Ad	bronchial
9	chr1:97507800-97508600	Weak transcription	Osteobl	bone
10	chr1:97508000-97508600	Weak transcription	NHDF-Ad	bronchial
11	chr1:97508200-97509000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
12	chr1:97508200-97509000	Enhancers	NHEK	skin
13	chr1:97508400-97509200	Enhancers	HMEC	breast
14	chr1:97508600-97508800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr1:97508600-97509000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
16	chr1:97508600-97509000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
17	chr1:97508600-97509400	ZNF genes & repeats	NHDF-Ad	bronchial
18	chr1:97508600-97509400	Enhancers	Osteobl	bone
19	chr1:97508800-97510200	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin01	Skin
20	chr1:97508800-97514800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
21	chr1:97509000-97509400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
22	chr1:97512200-97512800	Enhancers	Fetal Brain Female	brain
23	chr1:97512200-97512800	Enhancers	Rectal Smooth Muscle	rectum
24	chr1:97512400-97512600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
25	chr1:97512400-97512800	Enhancers	Sigmoid Colon	Sigmoid Colon
26	chr1:97512400-97513200	Enhancers	Adipose Nuclei	Adipose
27	chr1:97512400-97513600	Enhancers	Fetal Brain Male	brain
28	chr1:97512600-97513200	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
29	chr1:97512600-97513200	Enhancers	Colon Smooth Muscle	Colon
30	chr1:97512600-97513200	Enhancers	Fetal Muscle Trunk	muscle
31	chr1:97512600-97514000	Enhancers	Fetal Muscle Leg	muscle
32	chr1:97512800-97516000	Weak transcription	Rectal Smooth Muscle	rectum
33	chr1:97513200-97514400	Weak transcription	Colon Smooth Muscle	Colon
34	chr1:97513200-97514800	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
35	chr1:97514000-97514800	Active TSS	Fetal Muscle Leg	muscle
36	chr1:97514200-97514400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
37	chr1:97514400-97514600	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
38	chr1:97514400-97514600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
39	chr1:97514400-97514800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
40	chr1:97514400-97515000	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chr1:97514400-97515000	Active TSS	A549	lung
42	chr1:97514400-97515600	Enhancers	Colon Smooth Muscle	Colon
43	chr1:97514600-97515000	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
44	chr1:97514600-97515000	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
45	chr1:97514600-97515000	Active TSS	NHDF-Ad	bronchial
46	chr1:97514600-97515000	Active TSS	Osteobl	bone
47	chr1:97514800-97515000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
48	chr1:97514800-97516000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
49	chr1:97515000-97516600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
50	chr1:97515000-97517600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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