Variant report

Variant	nsv546928
Chromosome Location	chr1:103331349-103371652
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:270)
CpG islands
(count:61)
Chromatin interactive
region (count:0)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:270 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CBX3	chr1:103344992-103345640	HCT-116	colon:	n/a	n/a
2	CEBPB	chr1:103344931-103345570	IMR90	lung:	n/a	n/a
3	CEBPB	chr1:103344973-103345668	HCT-116	colon:	n/a	n/a
4	CEBPB	chr1:103344992-103345511	A549	lung:	n/a	n/a
5	CEBPB	chr1:103363066-103363488	A549	lung:	n/a	n/a
6	CEBPB	chr1:103344985-103345539	A549	lung:	n/a	n/a
7	CEBPB	chr1:103344959-103345583	Hela-S3	cervix:	n/a	n/a
8	CEBPB	chr1:103363004-103363495	Hela-S3	cervix:	n/a	n/a
9	CHD2	chr1:103363173-103363438	Hela-S3	cervix:	n/a	n/a
10	CTCF	chr1:103337640-103337790	HRPEpiC	eye:	n/a	n/a
11	CTCF	chr1:103337760-103337910	HCPEpiC	choroid plexus:	n/a	n/a
12	CTCF	chr1:103337774-103337882	Fibrobl	skin:	n/a	n/a
13	CTCF	chr1:103337740-103337890	AoAF	blood vessel:	n/a	n/a
14	CTCF	chr1:103337800-103337950	BE2_C	brain:	n/a	n/a
15	CTCF	chr1:103337720-103337870	GM06990	blood:	n/a	n/a
16	CTCF	chr1:103337640-103337790	HA-sp	spinal cord:	n/a	n/a
17	CTCF	chr1:103337760-103337910	HA-sp	spinal cord:	n/a	n/a
18	CTCF	chr1:103337740-103337890	HBMEC	blood vessel:	n/a	n/a
19	CTCF	chr1:103337774-103337912	GM19238	blood:	n/a	n/a
20	CTCF	chr1:103337774-103337902	Gliobla	brain:	n/a	n/a
21	CTCF	chr1:103337760-103337910	HepG2	liver:	n/a	n/a
22	CTCF	chr1:103337811-103337910	ProgFib	skin:	n/a	n/a
23	CTCF	chr1:103337768-103337887	GM13977	blood:	n/a	n/a
24	CTCF	chr1:103337760-103337910	GM12873	blood:	n/a	n/a
25	CTCF	chr1:103337820-103337970	SAEC	small airway:	n/a	n/a
26	CTCF	chr1:103337780-103337930	GM06990	blood:	n/a	n/a
27	CTCF	chr1:103337781-103337901	H1-hESC	embryonic stem cell:	n/a	n/a
28	CTCF	chr1:103337760-103337910	GM12868	blood:	n/a	n/a
29	CTCF	chr1:103338197-103338269	GM13977	blood:	n/a	n/a
30	CTCF	chr1:103337747-103337912	GM12891	blood:	n/a	n/a
31	CTCF	chr1:103337740-103337890	GM12867	blood:	n/a	n/a
32	CTCF	chr1:103337788-103337882	K562	blood:	n/a	n/a
33	CTCF	chr1:103337780-103337930	GM12866	blood:	n/a	n/a
34	CTCF	chr1:103337760-103337910	GM12865	blood:	n/a	n/a
35	CTCF	chr1:103337780-103337930	AG04449	skin:	n/a	n/a
36	CTCF	chr1:103337800-103337950	GM12871	blood:	n/a	n/a
37	CTCF	chr1:103337780-103337930	MCF-7	breast:	n/a	n/a
38	CTCF	chr1:103337843-103337890	GM20000	blood:	n/a	n/a
39	CTCF	chr1:103337709-103337970	GM12878	blood:	n/a	n/a
40	CTCF	chr1:103337761-103337906	GM12878	blood:	n/a	n/a
41	CTCF	chr1:103337720-103337870	GM12875	blood:	n/a	n/a
42	CTCF	chr1:103337840-103337990	GM12874	blood:	n/a	n/a
43	CTCF	chr1:103337805-103337870	NHEK	skin:	n/a	n/a
44	CTCF	chr1:103337740-103337890	HUVEC	blood vessel:	n/a	n/a
45	CTCF	chr1:103337775-103337907	GM19240	blood:	n/a	n/a
46	CTCF	chr1:103337760-103337910	HMEC	breast:	n/a	n/a
47	CTCF	chr1:103337817-103337868	GM10266	blood:	n/a	n/a
48	CTCF	chr1:103337720-103337870	HPAF	blood vessel:	n/a	n/a
49	CTCF	chr1:103337760-103337910	HBMEC	blood vessel:	n/a	n/a
50	CTCF	chr1:103337770-103337898	HepG2	liver:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:103343469-103343519	SK-N-SH_RA	brain:	n/a
2	chr1:103343469-103343519	GM12892	blood:	n/a
3	chr1:103343469-103343519	K562	blood:	n/a
4	chr1:103343469-103343519	LNCaP	prostate:	n/a
5	chr1:103343469-103343519	HNPCEpiC	eye:	n/a
6	chr1:103343469-103343519	HRE	kidney:	n/a
7	chr1:103343469-103343519	AG09319	gingival:	n/a
8	chr1:103343469-103343519	IMR90	lung:	fetal
9	chr1:103343469-103343519	PrEC	prostate:	n/a
10	chr1:103343469-103343519	RPTEC	kidney:	n/a
11	chr1:103343469-103343519	NHDF-neo	bronchial:	n/a
12	chr1:103343469-103343519	HCPEpiC	choroid plexus:	n/a
13	chr1:103343469-103343519	GM19239	blood:	n/a
14	chr1:103343469-103343519	Caco-2	colon:	n/a
15	chr1:103343469-103343519	HCM	heart:	n/a
16	chr1:103343469-103343519	GM12891	blood:	n/a
17	chr1:103343469-103343519	Hepatocyte	liver:	n/a
18	chr1:103343469-103343519	HPAEpiC	pulmonary alveolar:	n/a
19	chr1:103343469-103343519	NT2-D1	testis:	n/a
20	chr1:103343469-103343519	PANC-1	pancreas:	n/a
21	chr1:103343469-103343519	AG04450	lung:	fetal
22	chr1:103343469-103343519	HUVEC	blood vessel:	n/a
23	chr1:103343469-103343519	A549	lung:	n/a
24	chr1:103343469-103343519	HMEC	breast:	n/a
25	chr1:103343469-103343519	SK-N-MC	brain:	n/a
26	chr1:103343469-103343519	HRCEpiC	kidney:	n/a
27	chr1:103343469-103343519	SAEC	small airway:	n/a
28	chr1:103343469-103343519	T-47D	breast:	n/a
29	chr1:103343469-103343519	HRPEpiC	eye:	n/a
30	chr1:103343469-103343519	HEEpiC	esophagus:	n/a
31	chr1:103343469-103343519	MCF-7	breast:	n/a
32	chr1:103343469-103343519	ProgFib	skin:	n/a
33	chr1:103343469-103343519	AG10803	skin:	n/a
34	chr1:103343469-103343519	HIPEpiC	eye:	n/a
35	chr1:103343469-103343519	SKMC	muscle:	n/a
36	chr1:103343469-103343519	U87	brain:	n/a
37	chr1:103343469-103343519	NH-A	brain:	n/a
38	chr1:103343469-103343519	SK-N-SH	brain:	n/a
39	chr1:103343469-103343519	H1-hESC	embryonic stem cell:	embryo
40	chr1:103343469-103343519	HCT-116	colon:	n/a
41	chr1:103343469-103343519	HL-60	blood:	n/a
42	chr1:103343469-103343519	HAEpiC	amniotic membrane:	n/a
43	chr1:103343469-103343519	HEK293	kidney:	embryo
44	chr1:103343469-103343519	MCF10A-Er-Src	breast:	n/a
45	chr1:103343469-103343519	HCF	heart:	n/a
46	chr1:103343469-103343519	AG09309	skin:	n/a
47	chr1:103343469-103343519	Jurkat	blood:	n/a
48	chr1:103343469-103343519	Hela-S3	cervix:	n/a
49	chr1:103343469-103343519	CMK	blood:	n/a
50	chr1:103343469-103343519	ovcar-3	ovarian:	n/a

No data

Variant related genes	Relation type
COL11A1	TF binding region
COL11A1	CpG island

Extended variants
information (count: 1670 )
Associated
traits (count: 102 )

Variant overlapped rSNPs/rCNVs (count:1670 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1020918	chr1:103331349-103331350	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs558476161	chr1:103331410-103331411	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs548351087	chr1:103331413-103331414	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs566994672	chr1:103331472-103331473	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs78252496	chr1:103331499-103331500	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs184039604	chr1:103331518-103331519	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs534199345	chr1:103331545-103331546	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs375888607	chr1:103331588-103331589	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs571433645	chr1:103331589-103331590	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs538899357	chr1:103331593-103331594	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs576943189	chr1:103331599-103331600	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs557316634	chr1:103331610-103331611	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs537839428	chr1:103331667-103331668	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs554166695	chr1:103331690-103331691	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs148582355	chr1:103331711-103331712	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs188434496	chr1:103331730-103331731	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs192214506	chr1:103331739-103331740	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs185097597	chr1:103331741-103331742	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs554361254	chr1:103331748-103331749	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs572941484	chr1:103331778-103331779	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs540449225	chr1:103331816-103331817	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs76823042	chr1:103331846-103331847	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs532589509	chr1:103331866-103331867	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs544456994	chr1:103331922-103331923	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs76754961	chr1:103331931-103331932	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs190787978	chr1:103331968-103331969	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs142794237	chr1:103331971-103331972	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs566829037	chr1:103331973-103331974	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs527817013	chr1:103331978-103331979	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs111458140	chr1:103331987-103331988	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs146059992	chr1:103332114-103332115	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs552404053	chr1:103332163-103332164	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs571441216	chr1:103332164-103332165	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs538841947	chr1:103332210-103332211	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs557253323	chr1:103332211-103332212	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs116694198	chr1:103332227-103332228	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs535868376	chr1:103332281-103332282	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs554579127	chr1:103332286-103332287	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs182084559	chr1:103332292-103332293	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs187195526	chr1:103332298-103332299	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs189241800	chr1:103332299-103332300	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs2783566	chr1:103332309-103332310	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs544442804	chr1:103332310-103332311	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs180770126	chr1:103332325-103332326	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs545719297	chr1:103332327-103332328	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs536139223	chr1:103332387-103332388	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs574818834	chr1:103332396-103332397	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs140100361	chr1:103332404-103332405	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs546124681	chr1:103332501-103332502	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs560501479	chr1:103332511-103332512	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:102)

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
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
Acute lymphoblastic leukemia	20435627	CNVD
Ovarian cancer	21720365	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Ewing''s sarcoma	17952124	CNVD
Cancer	22429812	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
Intestinal disease	21956041	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Schizophrenia	17879154	CNVD
Mental retardation	17124404	CNVD
Intestinal disease	17828263	CNVD
lymphocytic leukemia	21291569	CNVD
Colorectal cancer	16774939	CNVD
Myelofibrosis	22110671	CNVD
Lung adenocarcinoma	17086460	CNVD
Immune disease	21076436	CNVD
Immune disease	21042300	CNVD
Lung cancer	17086460	CNVD
Gastric cancer	16891809	CNVD
Breast cancer	22522925	CNVD
Chronic lymphocytic leukemia	21546498	CNVD

Chromatin state (count:269 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:103324800-103334200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr1:103334000-103349800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr1:103334200-103334800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr1:103335400-103350000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
5	chr1:103337800-103338200	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
6	chr1:103337800-103338200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr1:103338200-103340000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr1:103338400-103342800	Weak transcription	Cortex derived primary cultured neurospheres	brain
9	chr1:103338400-103343400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
10	chr1:103338400-103369400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr1:103338600-103342600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
12	chr1:103338600-103345000	Weak transcription	NH-A	brain
13	chr1:103338800-103357200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr1:103339000-103342600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr1:103339000-103345000	Weak transcription	HSMM	muscle
16	chr1:103339200-103349800	Weak transcription	HUES64 Cell Line	embryonic stem cell
17	chr1:103340000-103345200	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
18	chr1:103340800-103350000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
19	chr1:103341400-103345000	Weak transcription	HSMMtube	muscle
20	chr1:103341400-103349800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
21	chr1:103341600-103352000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
22	chr1:103342400-103349800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
23	chr1:103342600-103345200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
24	chr1:103342600-103345200	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
25	chr1:103342800-103346000	Strong transcription	Cortex derived primary cultured neurospheres	brain
26	chr1:103343000-103345800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
27	chr1:103343400-103345000	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
28	chr1:103343400-103352000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr1:103343400-103355800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
30	chr1:103343400-103356200	Weak transcription	Fetal Heart	heart
31	chr1:103343400-103366000	Weak transcription	Fetal Brain Female	brain
32	chr1:103344400-103349800	Weak transcription	H9 Cell Line	embryonic stem cell
33	chr1:103344600-103345000	Enhancers	A549	lung
34	chr1:103344800-103345000	Enhancers	Muscle Satellite Cultured Cells	--
35	chr1:103344800-103345000	Enhancers	Osteobl	bone
36	chr1:103344800-103345600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
37	chr1:103345000-103345200	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
38	chr1:103345000-103345200	Transcr. at gene 5' and 3'	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
39	chr1:103345000-103345200	Flanking Active TSS	Muscle Satellite Cultured Cells	--
40	chr1:103345000-103345400	Flanking Active TSS	NH-A	brain
41	chr1:103345000-103345600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
42	chr1:103345000-103345600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
43	chr1:103345000-103345600	Flanking Active TSS	A549	lung
44	chr1:103345000-103345600	Enhancers	Hela-S3	cervix
45	chr1:103345000-103345600	Enhancers	HSMMtube	muscle
46	chr1:103345000-103345600	Flanking Active TSS	Osteobl	bone
47	chr1:103345000-103345800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
48	chr1:103345000-103345800	Enhancers	NHDF-Ad	bronchial
49	chr1:103345000-103346000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
50	chr1:103345000-103346000	Enhancers	HSMM	muscle

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