Variant report

Variant	nsv871731
Chromosome Location	chr1:84597396-84658591
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:599)
CpG islands
(count:61)
Chromatin interactive
region (count:21)
LncRNA
region (count:13)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:599 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr1:84625274-84625597	K562	blood:	n/a	n/a
2	ATF2	chr1:84618224-84618863	GM12878	blood:	n/a	n/a
3	ATF3	chr1:84639743-84640360	A549	lung:	n/a	n/a
4	ATF3	chr1:84621649-84622441	HCT-116	colon:	n/a	n/a
5	BATF	chr1:84622058-84622350	GM12878	blood:	n/a	chr1:84622196-84622207
6	BATF	chr1:84618271-84618830	GM12878	blood:	n/a	n/a
7	BATF	chr1:84632577-84632840	GM12878	blood:	n/a	chr1:84632738-84632749
8	BATF	chr1:84618291-84618802	GM12878	blood:	n/a	n/a
9	BCL11A	chr1:84618300-84618565	GM12878	blood:	n/a	n/a
10	BCL11A	chr1:84618235-84618750	GM12878	blood:	n/a	n/a
11	BCLAF1	chr1:84618223-84618787	GM12878	blood:	n/a	n/a
12	BHLHE40	chr1:84622132-84622332	A549	lung:	n/a	n/a
13	CBX3	chr1:84612000-84612544	HCT-116	colon:	n/a	n/a
14	CBX3	chr1:84621472-84622485	HCT-116	colon:	n/a	n/a
15	CBX3	chr1:84609716-84610267	HCT-116	colon:	n/a	n/a
16	CBX3	chr1:84639712-84640465	HCT-116	colon:	n/a	n/a
17	CBX3	chr1:84621201-84622949	HCT-116	colon:	n/a	chr1:84621269-84621280
18	CBX3	chr1:84612020-84612700	HCT-116	colon:	n/a	n/a
19	CBX3	chr1:84639583-84640587	HCT-116	colon:	n/a	n/a
20	CEBPB	chr1:84641970-84642235	HepG2	liver:	n/a	chr1:84642138-84642149 chr1:84642137-84642150
21	CEBPB	chr1:84623013-84623236	IMR90	lung:	n/a	n/a
22	CEBPB	chr1:84621648-84622549	HCT-116	colon:	n/a	n/a
23	CEBPB	chr1:84639591-84640709	HCT-116	colon:	n/a	n/a
24	CEBPB	chr1:84646427-84646520	HepG2	liver:	n/a	n/a
25	CEBPB	chr1:84640217-84640541	A549	lung:	n/a	n/a
26	CEBPB	chr1:84639922-84640406	Hela-S3	cervix:	n/a	n/a
27	CEBPB	chr1:84621953-84622346	Hela-S3	cervix:	n/a	n/a
28	CEBPB	chr1:84641972-84642191	A549	lung:	n/a	chr1:84642138-84642149 chr1:84642137-84642150
29	CEBPB	chr1:84619166-84619515	IMR90	lung:	n/a	chr1:84619337-84619348
30	CEBPB	chr1:84641972-84642221	IMR90	lung:	n/a	chr1:84642138-84642149 chr1:84642137-84642150
31	CEBPB	chr1:84597961-84598264	HepG2	liver:	n/a	n/a
32	CEBPB	chr1:84606771-84607494	HCT-116	colon:	n/a	chr1:84607466-84607479 chr1:84607141-84607153 chr1:84607466-84607477
33	CEBPB	chr1:84611961-84612846	HCT-116	colon:	n/a	n/a
34	CEBPB	chr1:84619289-84619449	HepG2	liver:	n/a	chr1:84619337-84619348
35	CEBPB	chr1:84639642-84640513	HCT-116	colon:	n/a	n/a
36	CEBPB	chr1:84614426-84614628	HepG2	liver:	n/a	n/a
37	CTCF	chr1:84606780-84606930	HAc	cerebellar:	n/a	n/a
38	CTCF	chr1:84651926-84651993	NHEK	skin:	n/a	n/a
39	CTCF	chr1:84609866-84609954	Spleen_OC	spleen:	n/a	n/a
40	CTCF	chr1:84606901-84607212	Spleen_OC	spleen:	n/a	chr1:84607047-84607068
41	CTCF	chr1:84609959-84609983	Spleen_OC	spleen:	n/a	n/a
42	CTCF	chr1:84651897-84651999	HUVEC	blood vessel:	n/a	n/a
43	CTCF	chr1:84651940-84652090	RPTEC	kidney:	n/a	n/a
44	CTCF	chr1:84607020-84607170	AG04450	lung:	n/a	chr1:84607047-84607068
45	CTCF	chr1:84606995-84607095	GM20000	blood:	n/a	chr1:84607047-84607068
46	CTCF	chr1:84606880-84607030	BE2_C	brain:	n/a	n/a
47	CTCF	chr1:84606900-84607050	GM12873	blood:	n/a	n/a
48	CTCF	chr1:84652160-84652310	GM12868	blood:	n/a	n/a
49	CTCF	chr1:84606960-84607110	SAEC	small airway:	n/a	chr1:84607047-84607068
50	CTCF	chr1:84607020-84607170	GM12870	blood:	n/a	chr1:84607047-84607068

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:84609007-84609057	HCPEpiC	choroid plexus:	n/a
2	chr1:84609007-84609057	SAEC	small airway:	n/a
3	chr1:84609007-84609057	NHBE	bronchial:	n/a
4	chr1:84609007-84609057	HAEpiC	amniotic membrane:	n/a
5	chr1:84609007-84609057	MCF10A-Er-Src	breast:	n/a
6	chr1:84609007-84609057	HCM	heart:	n/a
7	chr1:84609007-84609057	HL-60	blood:	n/a
8	chr1:84609007-84609057	HMEC	breast:	n/a
9	chr1:84609007-84609057	LNCaP	prostate:	n/a
10	chr1:84609007-84609057	PANC-1	pancreas:	n/a
11	chr1:84609007-84609057	ProgFib	skin:	n/a
12	chr1:84609007-84609057	AG09319	gingival:	n/a
13	chr1:84609007-84609057	K562	blood:	n/a
14	chr1:84609007-84609057	GM06990	blood:	n/a
15	chr1:84609007-84609057	AG04449	skin:	fetal
16	chr1:84609007-84609057	SKMC	muscle:	n/a
17	chr1:84609007-84609057	Caco-2	colon:	n/a
18	chr1:84609007-84609057	AG04450	lung:	fetal
19	chr1:84609007-84609057	HUVEC	blood vessel:	n/a
20	chr1:84609007-84609057	A549	lung:	n/a
21	chr1:84609007-84609057	SK-N-MC	brain:	n/a
22	chr1:84609007-84609057	T-47D	breast:	n/a
23	chr1:84609007-84609057	AG10803	skin:	n/a
24	chr1:84609007-84609057	NH-A	brain:	n/a
25	chr1:84609007-84609057	NB4	blood:	n/a
26	chr1:84609007-84609057	NT2-D1	testis:	n/a
27	chr1:84609007-84609057	GM19239	blood:	n/a
28	chr1:84609007-84609057	SK-N-SH	brain:	n/a
29	chr1:84609007-84609057	Hepatocyte	liver:	n/a
30	chr1:84609007-84609057	U87	brain:	n/a
31	chr1:84609007-84609057	H1-hESC	embryonic stem cell:	embryo
32	chr1:84609007-84609057	GM12891	blood:	n/a
33	chr1:84609007-84609057	HEK293	kidney:	embryo
34	chr1:84609007-84609057	ovcar-3	ovarian:	n/a
35	chr1:84609007-84609057	NHDF-neo	bronchial:	n/a
36	chr1:84609007-84609057	HepG2	liver:	n/a
37	chr1:84609007-84609057	HCT-116	colon:	n/a
38	chr1:84609007-84609057	HRCEpiC	kidney:	n/a
39	chr1:84609007-84609057	GM12892	blood:	n/a
40	chr1:84609007-84609057	SK-N-SH_RA	brain:	n/a
41	chr1:84609007-84609057	BE2_C	brain:	n/a
42	chr1:84609007-84609057	BJ	skin:	n/a
43	chr1:84609007-84609057	Hela-S3	cervix:	n/a
44	chr1:84609007-84609057	PFSK-1	brain:	n/a
45	chr1:84609007-84609057	AoSMC	blood vessel:	n/a
46	chr1:84609007-84609057	IMR90	lung:	fetal
47	chr1:84609007-84609057	MCF-7	breast:	n/a
48	chr1:84609007-84609057	HRPEpiC	eye:	n/a
49	chr1:84609007-84609057	HCF	heart:	n/a
50	chr1:84609007-84609057	CMK	blood:	n/a

(count:21 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:84633326..84636042-chr1:84640053..84642677,3	K562	blood:
2	chr1:84639501..84640001-chr11:32381239..32382124,2	MCF-7	breast:
3	chr1:84633326..84635826-chr1:84640053..84642677,3	K562	blood:
4	chr1:84606627..84607493-chr1:84899132..84900125,4	MCF-7	breast:
5	chr1:84619466..84621949-chr1:84622598..84626604,3	K562	blood:
6	chr1:84594754..84597545-chr1:84597865..84602064,4	K562	blood:
7	chr1:84633326..84636042-chr1:84640053..84642677,3	K562	blood:
8	chr1:84639020..84640539-chr1:84647151..84649519,2	MCF-7	breast:
9	chr1:84628795..84632177-chr1:84635427..84638265,3	K562	blood:
10	chr1:84540791..84543154-chr1:84633401..84635166,2	K562	blood:
11	chr1:84587966..84589963-chr1:84603179..84604852,2	K562	blood:
12	chr1:84545204..84547427-chr1:84607809..84609728,2	K562	blood:
13	chr1:84596861..84598405-chr1:84603464..84605048,2	K562	blood:
14	chr1:84639020..84640539-chr1:84647151..84649519,2	MCF-7	breast:
15	chr1:84619466..84621949-chr1:84622598..84626604,3	K562	blood:
16	chr1:84606626..84607485-chr1:85006757..85007586,2	MCF-7	breast:
17	chr1:84596861..84598405-chr1:84603464..84605048,2	K562	blood:
18	chr1:84642752..84644786-chr1:84646959..84648659,2	K562	blood:
19	chr1:84594754..84597545-chr1:84597865..84602064,4	K562	blood:
20	chr1:84633326..84635826-chr1:84640053..84642677,3	K562	blood:
21	chr1:84606589..84609383-chr1:85086485..85089260,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SAMD13-1	chr1:84630387-84630696	NONHSAT004188
2	lnc-SAMD13-1	chr1:84644860-84644921	NONHSAT004188
3	lnc-SAMD13-1	chr1:84639012-84639035	NONHSAT004190
4	lnc-SAMD13-1	chr1:84644861-84644903	NONHSAT004191
5	lnc-SAMD13-1	chr1:84639013-84639035	NONHSAT004191
6	lnc-SAMD13-1	chr1:84630580-84630696	NONHSAT004190
7	lnc-SAMD13-1	chr1:84630581-84630696	NONHSAT004191
8	lnc-SAMD13-1	chr1:84644860-84644903	NONHSAT004190
9	lnc-SAMD13-1	chr1:84641482-84641490	NONHSAT004190
10	lnc-SAMD13-1	chr1:84640717-84640739	NONHSAT004191
11	lnc-SAMD13-1	chr1:84639012-84639035	NONHSAT004188
12	lnc-SAMD13-1	chr1:84640716-84640739	NONHSAT004188
13	lnc-SAMD13-1	chr1:84640716-84640739	NONHSAT004190

No data

Variant related genes	Relation type
PRKACB	TF binding region
PRKACB	CpG island
ENSG00000142875	chromatin interactions
GCH1	miRNA target sites
GCFC1	miRNA target sites
GCNT2	miRNA target sites

Extended variants
information (count: 1934 )
Associated
traits (count: 103 )

Variant overlapped rSNPs/rCNVs (count:1934 , 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	rs11163907	chr1:84597396-84597397	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs576473576	chr1:84597399-84597400	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs115276423	chr1:84597426-84597427	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs190450592	chr1:84597519-84597520	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs143152905	chr1:84597526-84597527	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs567704161	chr1:84597537-84597538	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs530116243	chr1:84597542-84597543	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs547144677	chr1:84597587-84597588	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs181991790	chr1:84597612-84597613	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs549476184	chr1:84597651-84597652	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs538728473	chr1:84597701-84597702	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs375269171	chr1:84597706-84597707	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs559109925	chr1:84597716-84597717	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs184402902	chr1:84597731-84597732	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs369543058	chr1:84597758-84597759	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs74095507	chr1:84597767-84597768	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs148216212	chr1:84597793-84597794	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs11163908	chr1:84597803-84597804	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs574120839	chr1:84597832-84597833	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs376180911	chr1:84597869-84597870	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs371405838	chr1:84597967-84597968	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs397862706	chr1:84597971-84597972	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs192993403	chr1:84597973-84597974	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs553319498	chr1:84597981-84597982	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs369205062	chr1:84598060-84598061	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs557876807	chr1:84598237-84598238	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs576553179	chr1:84598254-84598255	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs141258907	chr1:84598275-84598276	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs577018532	chr1:84598324-84598325	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs539370321	chr1:84598337-84598338	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs189209551	chr1:84598343-84598344	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs541990049	chr1:84598364-84598365	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs542154084	chr1:84598381-84598382	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs181182581	chr1:84598387-84598388	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs530153073	chr1:84598427-84598428	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs111571292	chr1:84598527-84598528	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs144083553	chr1:84598609-84598610	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs2684910	chr1:84598610-84598611	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs185883532	chr1:84598756-84598757	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs148712578	chr1:84598789-84598790	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs372330160	chr1:84598792-84598793	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs115996631	chr1:84598857-84598858	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs111829792	chr1:84598882-84598883	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs564322897	chr1:84598894-84598895	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs189129108	chr1:84598900-84598901	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs538032146	chr1:84598958-84598959	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs548503667	chr1:84598984-84598985	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs7512288	chr1:84599007-84599008	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs199912917	chr1:84599011-84599012	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs137863678	chr1:84599036-84599037	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:103)

Disease	PMID	Source
Medulloblastoma	21979893	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
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
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
Breast cancer	17133270	CNVD
Type 2 diabetes	21956041	CNVD
Uveal melanoma	20484589	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Ewing''s sarcoma	17952124	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Poland''s syndrome	22110015	CNVD
Glioblastoma multiforme	22286061	CNVD
Glioblastoma multiforme	21922591	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Cancer	22429812	CNVD
Effusion lymphoma	18079361	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
small cell lung cancer	20016488	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Multiple myeloma	17550852	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:1464 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:84569200-84599600	Weak transcription	Cortex derived primary cultured neurospheres	brain
2	chr1:84584000-84609600	Weak transcription	HSMM	muscle
3	chr1:84584000-84609800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr1:84588000-84618400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
5	chr1:84590600-84607400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr1:84592400-84599200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr1:84596800-84609000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
8	chr1:84597200-84598200	Enhancers	HepG2	liver
9	chr1:84597400-84598000	Enhancers	Stomach Mucosa	stomach
10	chr1:84598000-84598400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
11	chr1:84598400-84600600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
12	chr1:84599000-84599400	Enhancers	Monocytes-CD14+_RO01746	blood
13	chr1:84599200-84599600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr1:84599200-84599600	Enhancers	Pancreas	Pancrea
15	chr1:84599200-84599600	Active TSS	Spleen	Spleen
16	chr1:84599200-84601600	Enhancers	Dnd41	blood
17	chr1:84600000-84604400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr1:84600400-84600600	Enhancers	Primary T regulatory cells fromperipheralblood	blood
19	chr1:84600400-84601600	Enhancers	Primary T helper cells PMA-I stimulated	--
20	chr1:84600600-84601200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
21	chr1:84600600-84601200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
22	chr1:84600600-84601400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
23	chr1:84600800-84601200	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
24	chr1:84600800-84601600	Enhancers	Primary T cells from cord blood	blood
25	chr1:84600800-84601600	Enhancers	Primary T helper cells fromperipheralblood	blood
26	chr1:84601000-84601400	Enhancers	Primary T helper naive cells from peripheral blood	blood
27	chr1:84601000-84601400	Enhancers	Primary T killer memory cells from peripheral blood	blood
28	chr1:84601000-84601600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
29	chr1:84601400-84608600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
30	chr1:84601400-84608800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
31	chr1:84601600-84607000	Weak transcription	Primary T cells from cord blood	blood
32	chr1:84606400-84606600	Enhancers	A549	lung
33	chr1:84606600-84607400	Weak transcription	A549	lung
34	chr1:84606800-84607000	Enhancers	Brain Angular Gyrus	brain
35	chr1:84606800-84609400	Enhancers	Primary T helper cells PMA-I stimulated	--
36	chr1:84607000-84607200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
37	chr1:84607000-84607400	Active TSS	Pancreatic Islets	Pancreatic Islet
38	chr1:84607000-84609000	Enhancers	Primary T cells from cord blood	blood
39	chr1:84607000-84613600	Weak transcription	Brain Angular Gyrus	brain
40	chr1:84607200-84607400	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
41	chr1:84607200-84607600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr1:84607200-84607600	Enhancers	Rectal Mucosa Donor 31	rectum
43	chr1:84607200-84607800	Enhancers	Liver	Liver
44	chr1:84607200-84607800	Enhancers	Monocytes-CD14+_RO01746	blood
45	chr1:84607200-84609600	Enhancers	Primary hematopoietic stem cells	blood
46	chr1:84607200-84609600	Enhancers	Primary hematopoietic stem cells short term culture	blood
47	chr1:84607200-84609600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
48	chr1:84607200-84609800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
49	chr1:84607200-84609800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
50	chr1:84607200-84609800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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