Variant report

Variant	nsv999294
Chromosome Location	chr1:210598729-210612528
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:84)
CpG islands
(count:122)
Chromatin interactive
region (count:5)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:84 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF3	chr1:210612457-210612901	A549	lung:	n/a	n/a
2	ATF3	chr1:210612405-210612891	A549	lung:	n/a	n/a
3	CEBPB	chr1:210612131-210613087	IMR90	lung:	n/a	n/a
4	CEBPB	chr1:210612073-210612902	A549	lung:	n/a	n/a
5	CREB1	chr1:210612249-210612449	A549	lung:	n/a	n/a
6	CREB1	chr1:210612246-210612516	A549	lung:	n/a	n/a
7	EP300	chr1:210612135-210613075	A549	lung:	n/a	n/a
8	EP300	chr1:210611954-210613174	A549	lung:	n/a	n/a
9	EP300	chr1:210612017-210613121	SK-N-SH	brain:	n/a	n/a
10	FOS	chr1:210612276-210612788	HUVEC	blood vessel:	n/a	n/a
11	FOS	chr1:210612291-210612413	MCF10A-Er-Src	breast:	n/a	n/a
12	FOSL2	chr1:210612173-210612801	A549	lung:	n/a	n/a
13	FOSL2	chr1:210612134-210612848	SK-N-SH	brain:	n/a	n/a
14	FOSL2	chr1:210612155-210613060	SK-N-SH	brain:	n/a	n/a
15	FOSL2	chr1:210612077-210613020	A549	lung:	n/a	n/a
16	GABPA	chr1:210612097-210612948	A549	lung:	n/a	n/a
17	GATA2	chr1:210612263-210612816	HUVEC	blood vessel:	n/a	chr1:210612652-210612666
18	GATA3	chr1:210611948-210613213	A549	lung:	n/a	n/a
19	GATA3	chr1:210612023-210613152	SK-N-SH	brain:	n/a	n/a
20	GATA3	chr1:210612036-210613265	SK-N-SH	brain:	n/a	n/a
21	GATA3	chr1:210612109-210612914	A549	lung:	n/a	n/a
22	HDAC2	chr1:210607624-210607832	H1-hESC	embryonic stem cell:	n/a	n/a
23	JUND	chr1:210612101-210613143	SK-N-SH	brain:	n/a	n/a
24	JUND	chr1:210607638-210607959	H1-hESC	embryonic stem cell:	n/a	n/a
25	JUND	chr1:210612051-210613036	SK-N-SH	brain:	n/a	n/a
26	JUND	chr1:210612208-210612856	A549	lung:	n/a	n/a
27	JUND	chr1:210610549-210610692	HepG2	liver:	n/a	n/a
28	JUND	chr1:210610724-210610771	K562	blood:	n/a	n/a
29	MAFK	chr1:210612136-210613448	IMR90	lung:	n/a	n/a
30	MAX	chr1:210612191-210613010	SK-N-SH	brain:	n/a	n/a
31	MAX	chr1:210612202-210612472	A549	lung:	n/a	n/a
32	MAX	chr1:210612181-210612942	SK-N-SH	brain:	n/a	n/a
33	MAX	chr1:210611980-210613201	A549	lung:	n/a	n/a
34	MAX	chr1:210612048-210613046	A549	lung:	n/a	n/a
35	MAZ	chr1:210612075-210614083	IMR90	lung:	n/a	n/a
36	MYC	chr1:210612320-210612419	H1-hESC	embryonic stem cell:	n/a	n/a
37	MYC	chr1:210612214-210612909	MCF10A-Er-Src	breast:	n/a	n/a
38	NFIC	chr1:210612072-210613136	SK-N-SH	brain:	n/a	n/a
39	NR3C1	chr1:210612253-210612517	A549	lung:	n/a	n/a
40	NR3C1	chr1:210612146-210612588	A549	lung:	n/a	n/a
41	NR3C1	chr1:210612282-210612528	A549	lung:	n/a	n/a
42	NR3C1	chr1:210612184-210612875	A549	lung:	n/a	n/a
43	PBX3	chr1:210612059-210613098	SK-N-SH	brain:	n/a	n/a
44	PBX3	chr1:210612078-210613098	SK-N-SH	brain:	n/a	n/a
45	POLR2A	chr1:210612162-210612936	SK-N-SH	brain:	n/a	n/a
46	POLR2A	chr1:210599244-210599425	K562	blood:	n/a	n/a
47	POLR2A	chr1:210612435-210612453	ProgFib	skin:	n/a	n/a
48	POLR2A	chr1:210611651-210611653	ProgFib	skin:	n/a	n/a
49	POLR2A	chr1:210602169-210602327	A549	lung:	n/a	n/a
50	POLR2A	chr1:210605815-210606105	K562	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:210607796-210607846	NHBE	bronchial:	n/a
2	chr1:210612391-210612441	SKMC	muscle:	n/a
3	chr1:210607796-210607846	SK-N-MC	brain:	n/a
4	chr1:210612391-210612441	HPAEpiC	pulmonary alveolar:	n/a
5	chr1:210607796-210607846	SAEC	small airway:	n/a
6	chr1:210607796-210607846	HEEpiC	esophagus:	n/a
7	chr1:210607796-210607846	SK-N-SH_RA	brain:	n/a
8	chr1:210612391-210612441	Hela-S3	cervix:	n/a
9	chr1:210607796-210607846	PrEC	prostate:	n/a
10	chr1:210612391-210612441	MCF-7	breast:	n/a
11	chr1:210607796-210607846	PFSK-1	brain:	n/a
12	chr1:210607796-210607846	HCF	heart:	n/a
13	chr1:210607796-210607846	U87	brain:	n/a
14	chr1:210612391-210612441	HIPEpiC	eye:	n/a
15	chr1:210607796-210607846	HNPCEpiC	eye:	n/a
16	chr1:210607796-210607846	HRCEpiC	kidney:	n/a
17	chr1:210607796-210607846	BE2_C	brain:	n/a
18	chr1:210607796-210607846	SKMC	muscle:	n/a
19	chr1:210607796-210607846	NT2-D1	testis:	n/a
20	chr1:210607796-210607846	AG09319	gingival:	n/a
21	chr1:210607796-210607846	HL-60	blood:	n/a
22	chr1:210612391-210612441	Caco-2	colon:	n/a
23	chr1:210612391-210612441	T-47D	breast:	n/a
24	chr1:210612391-210612441	MCF10A-Er-Src	breast:	n/a
25	chr1:210612391-210612441	HUVEC	blood vessel:	n/a
26	chr1:210612391-210612441	HCM	heart:	n/a
27	chr1:210612391-210612441	RPTEC	kidney:	n/a
28	chr1:210612391-210612441	HCPEpiC	choroid plexus:	n/a
29	chr1:210607796-210607846	ECC-1	luminal epithelium:	n/a
30	chr1:210607796-210607846	NB4	blood:	n/a
31	chr1:210612391-210612441	HepG2	liver:	n/a
32	chr1:210607796-210607846	BJ	skin:	n/a
33	chr1:210612391-210612441	GM19239	blood:	n/a
34	chr1:210607796-210607846	AG04450	lung:	fetal
35	chr1:210607796-210607846	HRE	kidney:	n/a
36	chr1:210612391-210612441	PFSK-1	brain:	n/a
37	chr1:210607796-210607846	GM06990	blood:	n/a
38	chr1:210612391-210612441	HAEpiC	amniotic membrane:	n/a
39	chr1:210612391-210612441	NH-A	brain:	n/a
40	chr1:210612391-210612441	PANC-1	pancreas:	n/a
41	chr1:210612391-210612441	AG10803	skin:	n/a
42	chr1:210612391-210612441	HCF	heart:	n/a
43	chr1:210607796-210607846	IMR90	lung:	fetal
44	chr1:210607796-210607846	Jurkat	blood:	n/a
45	chr1:210612391-210612441	AoSMC	blood vessel:	n/a
46	chr1:210612391-210612441	NT2-D1	testis:	n/a
47	chr1:210607796-210607846	NH-A	brain:	n/a
48	chr1:210612391-210612441	U87	brain:	n/a
49	chr1:210612391-210612441	BJ	skin:	n/a
50	chr1:210612391-210612441	HRCEpiC	kidney:	n/a

(count:5 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:210545308..210548162-chr1:210603373..210605975,2	MCF-7	breast:
2	chr1:210545786..210547818-chr1:210606420..210608180,2	K562	blood:
3	chr1:210545823..210547818-chr1:210606420..210608728,2	K562	blood:
4	chr1:210603462..210605610-chr1:210606812..210609556,2	MCF-7	breast:
5	chr1:210603462..210605610-chr1:210606812..210609556,2	MCF-7	breast:

No data

Variant related genes	Relation type
HHAT	TF binding region
HHAT	CpG island
ENSG00000200972	chromatin interactions

Extended variants
information (count: 581 )
Associated
traits (count: 97 )

Variant overlapped rSNPs/rCNVs (count:581 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs539080372	chr1:210598729-210598730	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs531946597	chr1:210598740-210598741	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs139768583	chr1:210598752-210598753	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs570057449	chr1:210598818-210598819	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs150055112	chr1:210598823-210598824	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs4845021	chr1:210598837-210598838	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
7	rs114055024	chr1:210598859-210598860	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs534830548	chr1:210598882-210598883	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs186509287	chr1:210598896-210598897	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs372499341	chr1:210598909-210598910	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs4845022	chr1:210598936-210598937	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs189876063	chr1:210598956-210598957	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs558080655	chr1:210598988-210598989	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs576261002	chr1:210598990-210598991	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs543563533	chr1:210599022-210599023	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs561750454	chr1:210599042-210599043	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs145197982	chr1:210599049-210599050	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs75296578	chr1:210599086-210599087	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs4845023	chr1:210599113-210599114	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs559062025	chr1:210599133-210599134	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs77717776	chr1:210599138-210599139	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs142270513	chr1:210599143-210599144	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs569972216	chr1:210599201-210599202	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs182518309	chr1:210599202-210599203	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs147910291	chr1:210599208-210599209	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs112406188	chr1:210599244-210599245	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs11119490	chr1:210599261-210599262	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs543792090	chr1:210599289-210599290	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs187137565	chr1:210599323-210599324	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs571818839	chr1:210599338-210599339	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs538988322	chr1:210599373-210599374	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs557401805	chr1:210599429-210599430	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs576253269	chr1:210599459-210599460	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs543329272	chr1:210599469-210599470	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs555667061	chr1:210599470-210599471	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs76867671	chr1:210599499-210599500	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs368906312	chr1:210599542-210599543	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs192042399	chr1:210599594-210599595	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs185043398	chr1:210599614-210599615	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs188754552	chr1:210599630-210599631	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs11119491	chr1:210599633-210599634	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs146987444	chr1:210599634-210599635	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs113511304	chr1:210599737-210599738	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs193004244	chr1:210599754-210599755	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs114236074	chr1:210599785-210599786	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs530557050	chr1:210599791-210599792	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs147607551	chr1:210599810-210599811	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs368463859	chr1:210599839-210599840	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs540106861	chr1:210599841-210599842	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs60399668	chr1:210599850-210599851	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:97)

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
Medulloblastoma	21979893	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	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
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
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
Breast cancer	21509527	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17393978	CNVD
Hepatocellular carcinoma	16750200	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Trisomy 5 syndrome	21098271	CNVD
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Chordoma	18071362	CNVD
Macular degeneration	22558131	CNVD
Alzheimer''s disease	21403675	CNVD
Multiple myeloma	16461302	CNVD
van der Woude syndrome	22470819	CNVD
van der Woude syndrome	20818247	CNVD
T-cell lymphomas	19863542	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	17060936	CNVD
Atypical hemolytic uremic syndrome	19861685	CNVD
Hepatocellular carcinoma	18803288	CNVD
Urothelial tumor	18831757	CNVD
Lung cancer	18438408	CNVD
Ovarian cancer	21720365	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Schizophrenia	20967226	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:87 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:210567400-210617200	Weak transcription	Left Ventricle	heart
2	chr1:210571400-210641000	Weak transcription	Duodenum Smooth Muscle	Duodenum
3	chr1:210586400-210610800	Weak transcription	Aorta	Aorta
4	chr1:210592000-210609400	Weak transcription	Ovary	ovary
5	chr1:210592800-210625000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
6	chr1:210600000-210600200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
7	chr1:210600600-210600800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
8	chr1:210601000-210607600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
9	chr1:210602000-210602400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr1:210602400-210613600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr1:210604200-210610000	Weak transcription	HSMM	muscle
12	chr1:210604400-210604600	Enhancers	HSMMtube	muscle
13	chr1:210604600-210607200	Weak transcription	HSMMtube	muscle
14	chr1:210605600-210605800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
15	chr1:210605600-210608000	Enhancers	ES-I3 Cell Line	embryonic stem cell
16	chr1:210605800-210606200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr1:210605800-210606800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
18	chr1:210606600-210607400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr1:210606600-210608000	Enhancers	H1 Cell Line	embryonic stem cell
20	chr1:210606600-210608000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
21	chr1:210606800-210608000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr1:210606800-210608000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
23	chr1:210606800-210608000	Enhancers	iPS-15b Cell Line	embryonic stem cell
24	chr1:210606800-210608200	Enhancers	HUES64 Cell Line	embryonic stem cell
25	chr1:210606800-210608200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
26	chr1:210606800-210608400	Enhancers	iPS-18 Cell Line	embryonic stem cell
27	chr1:210607000-210607400	Enhancers	iPS-20b Cell Line	embryonic stem cell
28	chr1:210607000-210608200	Enhancers	HUES48 Cell Line	embryonic stem cell
29	chr1:210607200-210608000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
30	chr1:210607200-210608200	Enhancers	HSMMtube	muscle
31	chr1:210607400-210607600	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
32	chr1:210607400-210608200	Enhancers	HUES6 Cell Line	embryonic stem cell
33	chr1:210607600-210608000	Enhancers	Muscle Satellite Cultured Cells	--
34	chr1:210607600-210608200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
35	chr1:210607600-210608200	Enhancers	iPS-20b Cell Line	embryonic stem cell
36	chr1:210608000-210608400	Weak transcription	Muscle Satellite Cultured Cells	--
37	chr1:210608000-210612000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
38	chr1:210608000-210612200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
39	chr1:210608200-210609800	Weak transcription	HSMMtube	muscle
40	chr1:210608200-210612200	Weak transcription	HUES6 Cell Line	embryonic stem cell
41	chr1:210608200-210612200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
42	chr1:210608200-210612800	Weak transcription	HUES48 Cell Line	embryonic stem cell
43	chr1:210608400-210608800	ZNF genes & repeats	Muscle Satellite Cultured Cells	--
44	chr1:210608800-210610200	Weak transcription	Muscle Satellite Cultured Cells	--
45	chr1:210609200-210619800	Weak transcription	Esophagus	oesophagus
46	chr1:210609800-210612800	Enhancers	HSMMtube	muscle
47	chr1:210610000-210610600	Genic enhancers	HSMM	muscle
48	chr1:210610200-210613800	Enhancers	Muscle Satellite Cultured Cells	--
49	chr1:210610600-210612400	Enhancers	HSMM	muscle
50	chr1:210610600-210612800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

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