Variant report

Variant	nsv548655
Chromosome Location	chr1:192259645-192372674
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:427)
CpG islands
(count:122)
Chromatin interactive
region (count:40)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:427 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:192280293-192280660	K562	blood:	n/a	n/a
2	ATF1	chr1:192272985-192273118	K562	blood:	n/a	n/a
3	ATF1	chr1:192368786-192368852	K562	blood:	n/a	n/a
4	ATF1	chr1:192344749-192344769	K562	blood:	n/a	n/a
5	ATF1	chr1:192356272-192356274	K562	blood:	n/a	n/a
6	ATF1	chr1:192275036-192275081	K562	blood:	n/a	n/a
7	ATF1	chr1:192355441-192355519	K562	blood:	n/a	n/a
8	BACH1	chr1:192285827-192285912	K562	blood:	n/a	n/a
9	BCL11A	chr1:192348057-192348306	GM12878	blood:	n/a	chr1:192348127-192348136
10	CBX3	chr1:192355006-192355437	K562	blood:	n/a	n/a
11	CBX3	chr1:192277478-192277742	K562	blood:	n/a	n/a
12	CBX3	chr1:192277415-192277815	K562	blood:	n/a	n/a
13	CCNT2	chr1:192344697-192344799	K562	blood:	n/a	n/a
14	CEBPB	chr1:192341423-192341669	A549	lung:	n/a	chr1:192341560-192341571
15	CEBPB	chr1:192341494-192341588	K562	blood:	n/a	chr1:192341560-192341571
16	CEBPB	chr1:192345552-192345934	A549	lung:	n/a	chr1:192345768-192345779 chr1:192345767-192345780 chr1:192345767-192345780
17	CEBPB	chr1:192278595-192278597	HepG2	liver:	n/a	n/a
18	CEBPB	chr1:192365717-192365902	IMR90	lung:	n/a	chr1:192365799-192365812
19	CEBPB	chr1:192345624-192345821	K562	blood:	n/a	chr1:192345767-192345780 chr1:192345767-192345780 chr1:192345768-192345779
20	CEBPB	chr1:192345590-192345945	IMR90	lung:	n/a	chr1:192345767-192345780 chr1:192345767-192345780 chr1:192345768-192345779
21	CEBPB	chr1:192345590-192345942	HepG2	liver:	n/a	chr1:192345767-192345780 chr1:192345767-192345780 chr1:192345768-192345779
22	CEBPB	chr1:192295560-192295826	K562	blood:	n/a	chr1:192295668-192295679 chr1:192295668-192295681
23	CEBPB	chr1:192299264-192299313	HepG2	liver:	n/a	n/a
24	CEBPB	chr1:192345612-192345905	Hela-S3	cervix:	n/a	chr1:192345767-192345780 chr1:192345767-192345780 chr1:192345768-192345779
25	CEBPB	chr1:192341411-192341725	H1-hESC	embryonic stem cell:	n/a	chr1:192341560-192341571
26	CEBPB	chr1:192345396-192345926	H1-hESC	embryonic stem cell:	n/a	chr1:192345767-192345780 chr1:192345767-192345780 chr1:192345768-192345779
27	CEBPB	chr1:192295571-192295831	HepG2	liver:	n/a	chr1:192295668-192295679 chr1:192295668-192295681
28	CEBPB	chr1:192266819-192267127	K562	blood:	n/a	chr1:192266996-192267007
29	CEBPB	chr1:192345557-192345966	MCF-7	breast:	n/a	chr1:192345767-192345780 chr1:192345767-192345780 chr1:192345768-192345779
30	CEBPB	chr1:192345488-192346019	A549	lung:	n/a	chr1:192345767-192345780 chr1:192345767-192345780 chr1:192345768-192345779
31	CEBPB	chr1:192345553-192345968	K562	blood:	n/a	chr1:192345767-192345780 chr1:192345767-192345780 chr1:192345768-192345779
32	CEBPB	chr1:192294118-192294318	HepG2	liver:	n/a	chr1:192294239-192294250
33	CEBPB	chr1:192355953-192356040	K562	blood:	n/a	n/a
34	CEBPB	chr1:192305030-192305200	HepG2	liver:	n/a	n/a
35	CEBPB	chr1:192281351-192281484	A549	lung:	n/a	n/a
36	CEBPB	chr1:192289480-192289498	HepG2	liver:	n/a	chr1:192289481-192289492
37	CEBPB	chr1:192341441-192341671	HepG2	liver:	n/a	chr1:192341560-192341571
38	CEBPB	chr1:192345585-192345944	A549	lung:	n/a	chr1:192345767-192345780 chr1:192345767-192345780 chr1:192345768-192345779
39	CEBPB	chr1:192345571-192346001	K562	blood:	n/a	chr1:192345767-192345780 chr1:192345767-192345780 chr1:192345768-192345779
40	CEBPB	chr1:192266856-192267080	HepG2	liver:	n/a	chr1:192266996-192267007
41	CEBPB	chr1:192351987-192352013	HepG2	liver:	n/a	n/a
42	CEBPB	chr1:192365693-192365863	K562	blood:	n/a	chr1:192365799-192365812
43	CHD2	chr1:192354972-192355271	K562	blood:	n/a	n/a
44	CTCF	chr1:192356008-192356068	Hela-S3	cervix:	n/a	n/a
45	CTCF	chr1:192352000-192352150	GM12872	blood:	n/a	n/a
46	CTCF	chr1:192280559-192280560	GM10266	blood:	n/a	n/a
47	CTCF	chr1:192351960-192352110	GM12874	blood:	n/a	n/a
48	CTCF	chr1:192280460-192280610	MCF-7	breast:	n/a	n/a
49	CTCF	chr1:192332360-192332510	HBMEC	blood vessel:	n/a	n/a
50	CTCF	chr1:192351980-192352130	BE2_C	brain:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:192304785-192304835	HRE	kidney:	n/a
2	chr1:192285333-192285383	HPAEpiC	pulmonary alveolar:	n/a
3	chr1:192304785-192304835	AG04449	skin:	fetal
4	chr1:192285333-192285383	NT2-D1	testis:	n/a
5	chr1:192304785-192304835	HCF	heart:	n/a
6	chr1:192285333-192285383	HepG2	liver:	n/a
7	chr1:192304785-192304835	HMEC	breast:	n/a
8	chr1:192304785-192304835	MCF-7	breast:	n/a
9	chr1:192304785-192304835	HPAEpiC	pulmonary alveolar:	n/a
10	chr1:192304785-192304835	ECC-1	luminal epithelium:	n/a
11	chr1:192285333-192285383	Caco-2	colon:	n/a
12	chr1:192304785-192304835	ovcar-3	ovarian:	n/a
13	chr1:192304785-192304835	AoSMC	blood vessel:	n/a
14	chr1:192304785-192304835	HRCEpiC	kidney:	n/a
15	chr1:192285333-192285383	T-47D	breast:	n/a
16	chr1:192304785-192304835	CMK	blood:	n/a
17	chr1:192285333-192285383	LNCaP	prostate:	n/a
18	chr1:192285333-192285383	NB4	blood:	n/a
19	chr1:192304785-192304835	HCM	heart:	n/a
20	chr1:192285333-192285383	AG09309	skin:	n/a
21	chr1:192285333-192285383	ProgFib	skin:	n/a
22	chr1:192304785-192304835	HAEpiC	amniotic membrane:	n/a
23	chr1:192304785-192304835	ProgFib	skin:	n/a
24	chr1:192285333-192285383	NHDF-neo	bronchial:	n/a
25	chr1:192304785-192304835	SK-N-MC	brain:	n/a
26	chr1:192304785-192304835	HL-60	blood:	n/a
27	chr1:192304785-192304835	HEK293	kidney:	embryo
28	chr1:192285333-192285383	SAEC	small airway:	n/a
29	chr1:192304785-192304835	PANC-1	pancreas:	n/a
30	chr1:192304785-192304835	HIPEpiC	eye:	n/a
31	chr1:192304785-192304835	Hela-S3	cervix:	n/a
32	chr1:192304785-192304835	HRPEpiC	eye:	n/a
33	chr1:192304785-192304835	BE2_C	brain:	n/a
34	chr1:192304785-192304835	RPTEC	kidney:	n/a
35	chr1:192304785-192304835	A549	lung:	n/a
36	chr1:192285333-192285383	Hepatocyte	liver:	n/a
37	chr1:192304785-192304835	HNPCEpiC	eye:	n/a
38	chr1:192304785-192304835	HCT-116	colon:	n/a
39	chr1:192304785-192304835	Caco-2	colon:	n/a
40	chr1:192304785-192304835	NH-A	brain:	n/a
41	chr1:192304785-192304835	Jurkat	blood:	n/a
42	chr1:192285333-192285383	HEEpiC	esophagus:	n/a
43	chr1:192285333-192285383	K562	blood:	n/a
44	chr1:192285333-192285383	HMEC	breast:	n/a
45	chr1:192304785-192304835	NHDF-neo	bronchial:	n/a
46	chr1:192304785-192304835	IMR90	lung:	fetal
47	chr1:192304785-192304835	AG09309	skin:	n/a
48	chr1:192304785-192304835	U87	brain:	n/a
49	chr1:192304785-192304835	SKMC	muscle:	n/a
50	chr1:192285333-192285383	HNPCEpiC	eye:	n/a

(count:40 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:192368188..192369973-chr1:192371853..192374450,2	K562	blood:
2	chr1:192344215..192347684-chr1:192348226..192352405,4	K562	blood:
3	chr1:192312588..192314663-chr1:192330429..192332047,2	K562	blood:
4	chr1:192353018..192355468-chr1:192363241..192364892,2	K562	blood:
5	chr1:192356695..192359398-chr1:192364454..192366779,3	K562	blood:
6	chr1:192371824..192373829-chr1:192377801..192380040,2	K562	blood:
7	chr1:192295956..192298127-chr1:192303697..192305809,2	K562	blood:
8	chr1:192344743..192346250-chr1:192353971..192356636,2	K562	blood:
9	chr1:192353018..192355468-chr1:192363241..192364892,2	K562	blood:
10	chr1:192296149..192298127-chr1:192303474..192305809,2	K562	blood:
11	chr1:192309320..192313053-chr1:192320479..192324101,4	K562	blood:
12	chr1:192314027..192317570-chr1:192318637..192321629,4	K562	blood:
13	chr1:192242181..192244363-chr1:192263112..192265270,2	K562	blood:
14	chr1:192368188..192369973-chr1:192371853..192374450,2	K562	blood:
15	chr1:192364251..192366273-chr1:192371276..192373537,2	K562	blood:
16	chr1:192296149..192298127-chr1:192303474..192305809,2	K562	blood:
17	chr1:192364251..192366273-chr1:192371276..192373537,2	K562	blood:
18	chr1:192315023..192317400-chr1:192318904..192321629,2	K562	blood:
19	chr1:192309320..192313053-chr1:192320479..192324101,4	K562	blood:
20	chr1:191962409..191963306-chr1:192269925..192270965,3	MCF-7	breast:
21	chr1:192307961..192309733-chr1:192310054..192313025,2	K562	blood:
22	chr1:192307961..192309733-chr1:192310054..192313025,2	K562	blood:
23	chr1:192370922..192372618-chr1:192374409..192375984,2	K562	blood:
24	chr1:192362224..192364335-chr1:192367712..192370018,2	K562	blood:
25	chr1:192315023..192317400-chr1:192318904..192321629,2	K562	blood:
26	chr1:192320095..192323308-chr1:192323829..192327005,3	K562	blood:
27	chr1:192336641..192337331-chr11:76756837..76757401,2	MCF-7	breast:
28	chr1:192338308..192341245-chr1:192344798..192346639,2	K562	blood:
29	chr1:192295956..192298127-chr1:192303697..192305809,2	K562	blood:
30	chr1:192338308..192341245-chr1:192344798..192346639,2	K562	blood:
31	chr1:192356695..192359398-chr1:192364454..192366779,3	K562	blood:
32	chr1:192312588..192314663-chr1:192330429..192332047,2	K562	blood:
33	chr1:192320095..192323308-chr1:192323829..192327005,3	K562	blood:
34	chr1:192362224..192364335-chr1:192367712..192370018,2	K562	blood:
35	chr1:191858532..191860860-chr1:192337438..192339553,2	K562	blood:
36	chr1:191962436..191963394-chr1:192279940..192280907,5	MCF-7	breast:
37	chr1:192372329..192375655-chr1:192377870..192380869,3	K562	blood:
38	chr1:192344215..192347684-chr1:192348226..192352405,4	K562	blood:
39	chr1:192344743..192346250-chr1:192353971..192356636,2	K562	blood:
40	chr1:192314027..192317570-chr1:192318637..192321629,4	K562	blood:

No data

Variant related genes	Relation type
RGS21	TF binding region
RGS21	CpG island
ENSG00000223344	chromatin interactions

Extended variants
information (count: 1979 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:1979 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6428092	chr1:192260413-192260414	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs113269255	chr1:192260473-192260474	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs375558063	chr1:192260478-192260479	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs560244278	chr1:192260534-192260535	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs541798370	chr1:192260611-192260612	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs540585978	chr1:192260631-192260632	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs77591859	chr1:192260668-192260669	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs545514965	chr1:192260719-192260720	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs146153174	chr1:192260745-192260746	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs527527463	chr1:192260749-192260750	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs527630255	chr1:192260791-192260792	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs372917679	chr1:192260798-192260799	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs537085482	chr1:192272216-192272217	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs7538387	chr1:192272286-192272287	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs546830566	chr1:192272311-192272312	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs572351760	chr1:192272329-192272330	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs77492362	chr1:192272404-192272405	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs367848627	chr1:192272442-192272443	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs140841081	chr1:192272493-192272494	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs182712783	chr1:192272502-192272503	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs540254906	chr1:192272503-192272504	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs144752381	chr1:192272518-192272519	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs545249847	chr1:192272538-192272539	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs565026099	chr1:192272545-192272546	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs535170538	chr1:192272551-192272552	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs36010140	chr1:192272584-192272585	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs562123503	chr1:192272607-192272608	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs112177979	chr1:192272619-192272620	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs550644237	chr1:192272631-192272632	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs113106337	chr1:192272650-192272651	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs183301487	chr1:192272691-192272692	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs546934036	chr1:192272808-192272809	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs566629429	chr1:192272811-192272812	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs189163780	chr1:192272829-192272830	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs552075022	chr1:192272872-192272873	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs571758146	chr1:192272892-192272893	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs80057298	chr1:192272909-192272910	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs556993214	chr1:192272917-192272918	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs544323659	chr1:192272947-192272948	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs141326568	chr1:192272948-192272949	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs573712351	chr1:192272950-192272951	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs377143628	chr1:192272957-192272958	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs200931499	chr1:192272958-192272959	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs536577043	chr1:192273089-192273090	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs147873258	chr1:192273156-192273157	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs139276858	chr1:192273218-192273219	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs183762793	chr1:192273227-192273228	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs545442906	chr1:192273266-192273267	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs113475955	chr1:192273292-192273293	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs558784724	chr1:192273304-192273305	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:95)

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
Lung cancer	18438408	CNVD
Breast cancer	21509527	CNVD
Endometrioid adenocarcinoma	16974079	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
Chronic lymphocytic leukemia	22228453	CNVD
Urothelial carcinoma	21177765	CNVD
Lung adenocarcinoma	17086460	CNVD
Lung cancer	17086460	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16272173	CNVD
Mental retardation	21062444	CNVD
Liver carcinoma	19366792	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:152 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:192260400-192260800	Enhancers	HUVEC	blood vessel
2	chr1:192272200-192273000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
3	chr1:192273000-192276400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
4	chr1:192276400-192276800	ZNF genes & repeats	IMR90 fetal lung fibroblasts Cell Line	lung
5	chr1:192280200-192280800	Enhancers	Dnd41	blood
6	chr1:192283200-192283600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
7	chr1:192283600-192286000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
8	chr1:192286000-192286600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
9	chr1:192291200-192292000	Enhancers	iPS-18 Cell Line	embryonic stem cell
10	chr1:192291600-192292200	Enhancers	Primary neutrophils fromperipheralblood	blood
11	chr1:192292200-192292400	Active TSS	Primary neutrophils fromperipheralblood	blood
12	chr1:192292400-192292600	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
13	chr1:192298800-192299400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr1:192298800-192299600	Enhancers	Fetal Intestine Large	intestine
15	chr1:192299400-192299600	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr1:192299600-192299800	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr1:192303600-192307000	Enhancers	HUES64 Cell Line	embryonic stem cell
18	chr1:192303800-192306800	Enhancers	HUES48 Cell Line	embryonic stem cell
19	chr1:192304000-192306000	Enhancers	iPS-15b Cell Line	embryonic stem cell
20	chr1:192304000-192308000	Enhancers	iPS-18 Cell Line	embryonic stem cell
21	chr1:192304600-192305800	Enhancers	ES-I3 Cell Line	embryonic stem cell
22	chr1:192305800-192307200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
23	chr1:192306000-192312200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
24	chr1:192307200-192307800	Enhancers	ES-I3 Cell Line	embryonic stem cell
25	chr1:192307800-192312000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
26	chr1:192308000-192312200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
27	chr1:192311200-192312800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
28	chr1:192311800-192312000	Enhancers	Muscle Satellite Cultured Cells	--
29	chr1:192312000-192312600	Flanking Active TSS	Muscle Satellite Cultured Cells	--
30	chr1:192312000-192312800	Enhancers	ES-I3 Cell Line	embryonic stem cell
31	chr1:192312000-192313000	Enhancers	HSMM	muscle
32	chr1:192312200-192312800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
33	chr1:192312200-192312800	Enhancers	HUES6 Cell Line	embryonic stem cell
34	chr1:192312200-192312800	Enhancers	iPS-15b Cell Line	embryonic stem cell
35	chr1:192312200-192312800	Enhancers	iPS-18 Cell Line	embryonic stem cell
36	chr1:192312200-192313000	Enhancers	HSMMtube	muscle
37	chr1:192312400-192312800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
38	chr1:192312600-192312800	Enhancers	Muscle Satellite Cultured Cells	--
39	chr1:192312600-192313000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
40	chr1:192312800-192318200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
41	chr1:192318200-192318600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
42	chr1:192318200-192319000	Enhancers	Fetal Lung	lung
43	chr1:192318400-192318800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr1:192319000-192319400	Weak transcription	Fetal Lung	lung
45	chr1:192319400-192319800	Enhancers	Fetal Lung	lung
46	chr1:192319600-192320000	Enhancers	Fetal Intestine Large	intestine
47	chr1:192319600-192320000	Enhancers	Fetal Muscle Leg	muscle
48	chr1:192325200-192326000	Enhancers	HUVEC	blood vessel
49	chr1:192327000-192327400	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
50	chr1:192327400-192328400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived

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