Variant report

Variant	nsv546631
Chromosome Location	chr1:79518810-79614989
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:359)
CpG islands
(count:61)
Chromatin interactive
region (count:4)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:359 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr1:79545497-79545905	H1-hESC	embryonic stem cell:	n/a	chr1:79545669-79545683
2	BCL11A	chr1:79604022-79604167	H1-hESC	embryonic stem cell:	n/a	n/a
3	BCL11A	chr1:79603898-79604245	H1-hESC	embryonic stem cell:	n/a	n/a
4	CEBPB	chr1:79583039-79583331	IMR90	lung:	n/a	chr1:79583176-79583189
5	CEBPB	chr1:79587579-79587715	H1-hESC	embryonic stem cell:	n/a	chr1:79587688-79587699 chr1:79587688-79587701 chr1:79587690-79587701
6	CEBPB	chr1:79587527-79587826	HepG2	liver:	n/a	chr1:79587688-79587699 chr1:79587688-79587701 chr1:79587690-79587701
7	CEBPB	chr1:79560648-79560811	HepG2	liver:	n/a	n/a
8	CEBPB	chr1:79521171-79521337	A549	lung:	n/a	n/a
9	CEBPB	chr1:79566107-79566454	IMR90	lung:	n/a	n/a
10	CEBPB	chr1:79571297-79571471	IMR90	lung:	n/a	n/a
11	CEBPB	chr1:79587509-79587865	IMR90	lung:	n/a	chr1:79587688-79587699 chr1:79587688-79587701 chr1:79587690-79587701
12	CEBPB	chr1:79594497-79595010	IMR90	lung:	n/a	chr1:79594917-79594928 chr1:79594917-79594928 chr1:79594917-79594930
13	CEBPB	chr1:79521185-79521360	H1-hESC	embryonic stem cell:	n/a	n/a
14	CEBPB	chr1:79521267-79521303	Hela-S3	cervix:	n/a	n/a
15	CEBPB	chr1:79603920-79604175	H1-hESC	embryonic stem cell:	n/a	n/a
16	CEBPD	chr1:79562158-79562660	K562	blood:	n/a	n/a
17	CHD1	chr1:79574652-79574670	GM12878	blood:	n/a	n/a
18	CTCF	chr1:79535600-79535750	HRPEpiC	eye:	n/a	n/a
19	CTCF	chr1:79608985-79608991	Kidney_OC	kidney:	n/a	n/a
20	CTCF	chr1:79535320-79535470	RPTEC	kidney:	n/a	n/a
21	CTCF	chr1:79535540-79535690	HPAF	blood vessel:	n/a	n/a
22	CTCF	chr1:79535760-79535910	RPTEC	kidney:	n/a	n/a
23	CTCF	chr1:79535780-79535930	RPTEC	kidney:	n/a	n/a
24	CTCF	chr1:79535580-79535730	AG10803	skin:	n/a	n/a
25	CTCF	chr1:79535740-79535890	GM12864	blood:	n/a	n/a
26	CTCF	chr1:79608992-79609011	Kidney_OC	kidney:	n/a	n/a
27	CTCF	chr1:79588940-79589090	HPAF	blood vessel:	n/a	n/a
28	CTCF	chr1:79535800-79535950	AG04450	lung:	n/a	n/a
29	CTCF	chr1:79545540-79545690	AG10803	skin:	n/a	n/a
30	CTCF	chr1:79545500-79545650	GM12866	blood:	n/a	n/a
31	CTCF	chr1:79589000-79589150	HCFaa	heart:	n/a	n/a
32	CTCF	chr1:79535620-79535770	GM12873	blood:	n/a	n/a
33	CTCF	chr1:79535540-79535690	GM12870	blood:	n/a	n/a
34	CTCF	chr1:79535520-79535670	HRE	kidney:	n/a	n/a
35	CTCF	chr1:79535960-79536110	NHEK	skin:	n/a	n/a
36	CTCF	chr1:79608525-79608630	GM20000	blood:	n/a	n/a
37	CTCF	chr1:79535680-79535830	HBMEC	blood vessel:	n/a	n/a
38	CTCF	chr1:79594520-79594670	AG04449	skin:	n/a	n/a
39	CTCF	chr1:79594480-79594630	HPAF	blood vessel:	n/a	n/a
40	CTCF	chr1:79535616-79535733	IMR90	lung:	n/a	n/a
41	CTCF	chr1:79588940-79589090	HPF	lung:	n/a	n/a
42	CTCF	chr1:79589024-79589124	Hela-S3	cervix:	n/a	n/a
43	CTCF	chr1:79535880-79536030	AG04450	lung:	n/a	n/a
44	CTCF	chr1:79535600-79535750	GM12867	blood:	n/a	n/a
45	CTCF	chr1:79588960-79589110	HPAF	blood vessel:	n/a	n/a
46	CTCF	chr1:79535680-79535830	HEEpiC	esophagus:	n/a	n/a
47	CTCF	chr1:79535680-79535830	AoAF	blood vessel:	n/a	n/a
48	CTCF	chr1:79590846-79590902	Hela-S3	cervix:	n/a	n/a
49	CTCF	chr1:79588960-79589110	RPTEC	kidney:	n/a	n/a
50	CTCF	chr1:79535820-79535970	GM06990	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:79594960-79595010	AG09309	skin:	n/a
2	chr1:79594960-79595010	HRE	kidney:	n/a
3	chr1:79594960-79595010	GM12891	blood:	n/a
4	chr1:79594960-79595010	IMR90	lung:	fetal
5	chr1:79594960-79595010	HRCEpiC	kidney:	n/a
6	chr1:79594960-79595010	SK-N-SH_RA	brain:	n/a
7	chr1:79594960-79595010	HUVEC	blood vessel:	n/a
8	chr1:79594960-79595010	HCM	heart:	n/a
9	chr1:79594960-79595010	ProgFib	skin:	n/a
10	chr1:79594960-79595010	ovcar-3	ovarian:	n/a
11	chr1:79594960-79595010	Hela-S3	cervix:	n/a
12	chr1:79594960-79595010	HCF	heart:	n/a
13	chr1:79594960-79595010	K562	blood:	n/a
14	chr1:79594960-79595010	HEK293	kidney:	embryo
15	chr1:79594960-79595010	HIPEpiC	eye:	n/a
16	chr1:79594960-79595010	SAEC	small airway:	n/a
17	chr1:79594960-79595010	NHDF-neo	bronchial:	n/a
18	chr1:79594960-79595010	SK-N-SH	brain:	n/a
19	chr1:79594960-79595010	HMEC	breast:	n/a
20	chr1:79594960-79595010	MCF10A-Er-Src	breast:	n/a
21	chr1:79594960-79595010	Jurkat	blood:	n/a
22	chr1:79594960-79595010	T-47D	breast:	n/a
23	chr1:79594960-79595010	AG04450	lung:	fetal
24	chr1:79594960-79595010	NHBE	bronchial:	n/a
25	chr1:79594960-79595010	HCT-116	colon:	n/a
26	chr1:79594960-79595010	HNPCEpiC	eye:	n/a
27	chr1:79594960-79595010	GM12892	blood:	n/a
28	chr1:79594960-79595010	HepG2	liver:	n/a
29	chr1:79594960-79595010	ECC-1	luminal epithelium:	n/a
30	chr1:79594960-79595010	Hepatocyte	liver:	n/a
31	chr1:79594960-79595010	H1-hESC	embryonic stem cell:	embryo
32	chr1:79594960-79595010	HCPEpiC	choroid plexus:	n/a
33	chr1:79594960-79595010	PFSK-1	brain:	n/a
34	chr1:79594960-79595010	CMK	blood:	n/a
35	chr1:79594960-79595010	AoSMC	blood vessel:	n/a
36	chr1:79594960-79595010	SKMC	muscle:	n/a
37	chr1:79594960-79595010	SK-N-MC	brain:	n/a
38	chr1:79594960-79595010	RPTEC	kidney:	n/a
39	chr1:79594960-79595010	PrEC	prostate:	n/a
40	chr1:79594960-79595010	AG04449	skin:	fetal
41	chr1:79594960-79595010	GM06990	blood:	n/a
42	chr1:79594960-79595010	NH-A	brain:	n/a
43	chr1:79594960-79595010	HL-60	blood:	n/a
44	chr1:79594960-79595010	NT2-D1	testis:	n/a
45	chr1:79594960-79595010	BE2_C	brain:	n/a
46	chr1:79594960-79595010	PANC-1	pancreas:	n/a
47	chr1:79594960-79595010	HEEpiC	esophagus:	n/a
48	chr1:79594960-79595010	A549	lung:	n/a
49	chr1:79594960-79595010	HRPEpiC	eye:	n/a
50	chr1:79594960-79595010	LNCaP	prostate:	n/a

(count:4 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:79536026..79538535-chr1:79539899..79541790,2	K562	blood:
2	chr1:79527063..79529337-chr1:79533334..79535055,2	K562	blood:
3	chr1:79527063..79529337-chr1:79533334..79535055,2	K562	blood:
4	chr1:79536026..79538535-chr1:79539899..79541790,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-IFI44-7	chr1:79562042-79562232	NONHSAT004086
2	lnc-IFI44-7	chr1:79562972-79563122	NONHSAT004086

No data

Variant related genes	Relation type
ENSG00000266388	TF binding region
PSAT1P3	TF binding region
ENSG00000266388	CpG island
PSAT1P3	CpG island

Extended variants
information (count: 2722 )
Associated
traits (count: 102 )

Variant overlapped rSNPs/rCNVs (count:2722 , 50 per page) page: 1 2 3 4 5 6 7 ... 55

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17102673	chr1:79518810-79518811	Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs551892334	chr1:79518856-79518857	Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs149749290	chr1:79518888-79518889	Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs71643220	chr1:79518938-79518939	Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs547972788	chr1:79518948-79518949	Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs71643221	chr1:79518963-79518964	Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs71643222	chr1:79518966-79518967	Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs538850461	chr1:79519005-79519006	Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs370630697	chr1:79519026-79519027	Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs61768996	chr1:79519047-79519048	Enhancers Flanking Active TSS Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs541225084	chr1:79519086-79519087	Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs146652743	chr1:79519110-79519111	Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs369278264	chr1:79519113-79519114	Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs536984870	chr1:79519116-79519117	Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs554941251	chr1:79519144-79519145	Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs573231985	chr1:79519168-79519169	Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs186428536	chr1:79519202-79519203	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs565383839	chr1:79519247-79519248	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs577386698	chr1:79519252-79519253	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs189702559	chr1:79519274-79519275	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs562707998	chr1:79519287-79519288	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs529830090	chr1:79519297-79519298	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs548513251	chr1:79519317-79519318	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs560966699	chr1:79519344-79519345	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs10493621	chr1:79519427-79519428	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs527288158	chr1:79519454-79519455	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs551707601	chr1:79519516-79519517	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs140236350	chr1:79519529-79519530	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs145340405	chr1:79519532-79519533	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs17102675	chr1:79519555-79519556	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs569461407	chr1:79519570-79519571	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs201448432	chr1:79519599-79519600	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs35224211	chr1:79519600-79519601	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs397863205	chr1:79519613-79519614	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs536438741	chr1:79519662-79519663	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs555254528	chr1:79519687-79519688	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs573412354	chr1:79519692-79519693	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs10493620	chr1:79519719-79519720	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
39	rs558960519	chr1:79519735-79519736	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs577297917	chr1:79519744-79519745	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs543187561	chr1:79519802-79519803	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs576348323	chr1:79519831-79519832	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs182292880	chr1:79519834-79519835	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs562840753	chr1:79519865-79519866	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs574614266	chr1:79519883-79519884	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs185139025	chr1:79519902-79519903	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs200731852	chr1:79519916-79519917	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs535877273	chr1:79519923-79519924	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs191065745	chr1:79520005-79520006	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs183283779	chr1:79520006-79520007	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:102)

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
Melanoma	17363583	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
Colorectal cancer	16774939	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:156 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:79517600-79519000	Enhancers	iPS-15b Cell Line	embryonic stem cell
2	chr1:79518400-79519000	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
3	chr1:79518400-79519000	Active TSS	Muscle Satellite Cultured Cells	--
4	chr1:79518400-79519000	Active TSS	Osteobl	bone
5	chr1:79518400-79519200	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr1:79518400-79519200	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr1:79518400-79519200	Active TSS	Adipose Nuclei	Adipose
8	chr1:79518400-79519200	Active TSS	GM12878-XiMat	blood
9	chr1:79518400-79519200	Active TSS	Monocytes-CD14+_RO01746	blood
10	chr1:79518600-79519000	Active TSS	Primary B cells from cord blood	blood
11	chr1:79518600-79519000	Active TSS	Primary T cells from cord blood	blood
12	chr1:79518600-79519000	Active TSS	Primary Natural Killer cells fromperipheralblood	blood
13	chr1:79518600-79519000	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
14	chr1:79518600-79519000	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
15	chr1:79518600-79519000	Active TSS	Brain Substantia Nigra	brain
16	chr1:79518600-79519000	Active TSS	Duodenum Mucosa	Duodenum
17	chr1:79518600-79519000	Active TSS	Duodenum Smooth Muscle	Duodenum
18	chr1:79518600-79519000	Active TSS	Rectal Mucosa Donor 29	rectum
19	chr1:79518600-79519000	Active TSS	Right Atrium	heart
20	chr1:79518600-79519000	Active TSS	Skeletal Muscle Female	skeletal muscle
21	chr1:79518600-79519000	Active TSS	A549	lung
22	chr1:79518600-79519000	Active TSS	Hela-S3	cervix
23	chr1:79518600-79519000	Active TSS	HMEC	breast
24	chr1:79518600-79519200	Active TSS	Primary monocytes fromperipheralblood	blood
25	chr1:79518600-79519200	Active TSS	HUVEC	blood vessel
26	chr1:79518800-79519000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
27	chr1:79518800-79519000	Enhancers	Primary B cells from peripheral blood	blood
28	chr1:79518800-79519000	Enhancers	Liver	Liver
29	chr1:79518800-79519000	Flanking Active TSS	NHDF-Ad	bronchial
30	chr1:79518800-79519000	Flanking Active TSS	NHLF	lung
31	chr1:79518800-79519200	Enhancers	ES-I3 Cell Line	embryonic stem cell
32	chr1:79518800-79519200	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
33	chr1:79518800-79519200	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
34	chr1:79518800-79519200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
35	chr1:79518800-79519200	Enhancers	Pancreatic Islets	Pancreatic Islet
36	chr1:79519000-79519200	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
37	chr1:79519000-79519200	Enhancers	Primary B cells from cord blood	blood
38	chr1:79519200-79525400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
39	chr1:79521600-79521800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
40	chr1:79522400-79523000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
41	chr1:79525400-79527600	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
42	chr1:79527600-79529400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
43	chr1:79536800-79538600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
44	chr1:79537000-79538800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
45	chr1:79544800-79548600	Enhancers	HUVEC	blood vessel
46	chr1:79545000-79546000	Enhancers	Adipose Nuclei	Adipose
47	chr1:79545200-79546000	Enhancers	HMEC	breast
48	chr1:79545200-79546000	Enhancers	NH-A	brain
49	chr1:79545200-79546000	Enhancers	NHDF-Ad	bronchial
50	chr1:79545200-79546200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

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