Variant report

Variant	nsv882846
Chromosome Location	chr5:128345803-128428962
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:479)
CpG islands
(count:0)
Chromatin interactive
region (count:40)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:479 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:128365722-128365760	K562	blood:	n/a	n/a
2	ARID3A	chr5:128410691-128410815	K562	blood:	n/a	n/a
3	ARID3A	chr5:128354593-128355004	K562	blood:	n/a	n/a
4	ARID3A	chr5:128419602-128419698	K562	blood:	n/a	n/a
5	ARID3A	chr5:128417730-128419210	K562	blood:	n/a	n/a
6	ARID3A	chr5:128409288-128409814	K562	blood:	n/a	n/a
7	ATF1	chr5:128399520-128399851	K562	blood:	n/a	n/a
8	ATF1	chr5:128410619-128410876	K562	blood:	n/a	n/a
9	ATF1	chr5:128417960-128418781	K562	blood:	n/a	n/a
10	ATF1	chr5:128387115-128387315	K562	blood:	n/a	n/a
11	ATF1	chr5:128354631-128354921	K562	blood:	n/a	n/a
12	ATF1	chr5:128414202-128414744	K562	blood:	n/a	n/a
13	ATF3	chr5:128414346-128414733	K562	blood:	n/a	n/a
14	BACH1	chr5:128380645-128380692	K562	blood:	n/a	n/a
15	BACH1	chr5:128426181-128426193	K562	blood:	n/a	n/a
16	BACH1	chr5:128409424-128409483	K562	blood:	n/a	n/a
17	BCL11A	chr5:128410492-128410820	GM12878	blood:	n/a	chr5:128410749-128410758
18	BHLHE40	chr5:128419554-128419803	K562	blood:	n/a	n/a
19	BHLHE40	chr5:128409215-128409433	K562	blood:	n/a	n/a
20	BHLHE40	chr5:128418003-128418806	K562	blood:	n/a	n/a
21	BRCA1	chr5:128403787-128403821	GM12878	blood:	n/a	n/a
22	CBX3	chr5:128417875-128418986	K562	blood:	n/a	n/a
23	CCNT2	chr5:128417880-128418897	K562	blood:	n/a	n/a
24	CCNT2	chr5:128367670-128367905	K562	blood:	n/a	chr5:128367773-128367793
25	CCNT2	chr5:128414115-128414667	K562	blood:	n/a	n/a
26	CCNT2	chr5:128354596-128354929	K562	blood:	n/a	chr5:128354783-128354803
27	CEBPB	chr5:128363920-128364215	IMR90	lung:	n/a	chr5:128364193-128364204
28	CEBPB	chr5:128363911-128364140	ECC-1	luminal epithelium:	n/a	n/a
29	CEBPB	chr5:128414415-128414701	K562	blood:	n/a	n/a
30	CEBPB	chr5:128417889-128418232	K562	blood:	n/a	n/a
31	CEBPB	chr5:128419068-128419398	K562	blood:	n/a	n/a
32	CEBPB	chr5:128420457-128420644	K562	blood:	n/a	n/a
33	CEBPB	chr5:128417739-128418883	K562	blood:	n/a	n/a
34	CEBPB	chr5:128419052-128419403	HepG2	liver:	n/a	n/a
35	CEBPB	chr5:128363920-128364207	HepG2	liver:	n/a	chr5:128364193-128364204
36	CEBPB	chr5:128410644-128410863	K562	blood:	n/a	n/a
37	CEBPB	chr5:128385280-128385478	HepG2	liver:	n/a	chr5:128385359-128385370
38	CEBPB	chr5:128417676-128418766	K562	blood:	n/a	n/a
39	CEBPB	chr5:128363953-128364194	K562	blood:	n/a	n/a
40	CEBPB	chr5:128410556-128410859	K562	blood:	n/a	n/a
41	CEBPB	chr5:128381880-128382153	H1-hESC	embryonic stem cell:	n/a	chr5:128382028-128382039
42	CEBPB	chr5:128381891-128382197	HepG2	liver:	n/a	chr5:128382028-128382039
43	CEBPB	chr5:128410531-128410898	Hela-S3	cervix:	n/a	n/a
44	CEBPB	chr5:128385198-128385472	K562	blood:	n/a	chr5:128385359-128385370
45	CEBPB	chr5:128424374-128424647	K562	blood:	n/a	n/a
46	CEBPB	chr5:128419634-128419846	K562	blood:	n/a	chr5:128419802-128419815
47	CEBPB	chr5:128363958-128364172	A549	lung:	n/a	n/a
48	CEBPB	chr5:128381893-128382207	Hela-S3	cervix:	n/a	chr5:128382028-128382039
49	CEBPB	chr5:128363884-128364169	H1-hESC	embryonic stem cell:	n/a	n/a
50	CEBPB	chr5:128418013-128418213	HepG2	liver:	n/a	n/a

No data

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

No.	Distal block	Cell Line	Cell type
1	chr5:128381531..128383297-chr5:128438091..128440053,2	K562	blood:
2	chr5:128416447..128420070-chr5:128432827..128437106,4	K562	blood:
3	chr5:128422228..128425056-chr5:128428398..128430336,2	K562	blood:
4	chr5:128411619..128415483-chr5:128416564..128419080,4	K562	blood:
5	chr5:128407324..128410452-chr5:128428795..128432000,3	K562	blood:
6	chr5:128416559..128421952-chr5:128424796..128432274,19	K562	blood:
7	chr5:128421308..128428287-chr5:128428713..128431869,7	MCF-7	breast:
8	chr20:48907747..48910180-chr5:128428330..128430095,2	MCF-7	breast:
9	chr5:128405381..128408939-chr5:128411989..128414861,3	K562	blood:
10	chr5:128404960..128406881-chr5:128413290..128414861,2	K562	blood:
11	chr5:128377612..128382273-chr5:128383539..128386141,4	K562	blood:
12	chr5:128426917..128432397-chr5:128432508..128439991,15	K562	blood:
13	chr5:128372433..128375040-chr5:128377244..128379501,2	K562	blood:
14	chr5:128393533..128395248-chr5:128398709..128400520,2	K562	blood:
15	chr5:128401270..128403695-chr5:128406645..128408852,2	MCF-7	breast:
16	chr5:128372433..128375040-chr5:128377244..128379501,2	K562	blood:
17	chr5:128416535..128420091-chr5:128429855..128432318,3	MCF-7	breast:
18	chr5:128422228..128425056-chr5:128428398..128430336,2	K562	blood:
19	chr5:128412002..128416464-chr5:128427958..128430736,3	MCF-7	breast:
20	chr5:128405381..128408939-chr5:128411989..128414861,3	K562	blood:
21	chr5:128404714..128406266-chr5:128419188..128421176,2	MCF-7	breast:
22	chr5:128404708..128406922-chr5:128429142..128431735,2	MCF-7	breast:
23	chr5:128401270..128403695-chr5:128406645..128408852,2	MCF-7	breast:
24	chr5:128374716..128377353-chr5:128379908..128382793,2	K562	blood:
25	chr5:128377612..128382273-chr5:128383539..128386141,4	K562	blood:
26	chr5:128425656..128428273-chr5:128428577..128431556,5	MCF-7	breast:
27	chr5:128404714..128406266-chr5:128419188..128421176,2	MCF-7	breast:
28	chr5:128362321..128365288-chr5:128368258..128370064,2	K562	blood:
29	chr5:128411619..128415483-chr5:128416564..128419080,4	K562	blood:
30	chr5:128419533..128421614-chr5:128429154..128430949,2	MCF-7	breast:
31	chr5:128407857..128410588-chr5:128417931..128419586,2	K562	blood:
32	chr5:128407922..128411228-chr5:128426698..128431846,6	MCF-7	breast:
33	chr5:128373872..128376064-chr5:128416925..128419708,2	K562	blood:
34	chr5:128299750..128303179-chr5:128428591..128431385,3	MCF-7	breast:
35	chr5:128362321..128365288-chr5:128368258..128370064,2	K562	blood:
36	chr5:128404960..128406881-chr5:128413290..128414861,2	K562	blood:
37	chr5:128373872..128376064-chr5:128416925..128419708,2	K562	blood:
38	chr5:128374716..128377353-chr5:128379908..128382793,2	K562	blood:
39	chr5:128393533..128395248-chr5:128398709..128400520,2	K562	blood:
40	chr5:128407857..128410588-chr5:128417931..128419586,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ISOC1-2	chr5:128422957-128423875	NONHSAT103665
2	lnc-ISOC1-2	chr5:128419938-128420050	NONHSAT103665

No data

Variant related genes	Relation type
MIR4633	TF binding region
ISOC1	TF binding region
ENSG00000113396	chromatin interactions
ENSG00000203999	chromatin interactions
ENSG00000066583	chromatin interactions
ENSG00000264563	chromatin interactions

Extended variants
information (count: 3111 )
Associated
traits (count: 77 )

Variant overlapped rSNPs/rCNVs (count:3111 , 50 per page) page: 1 2 3 4 5 6 7 ... 63

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1181972	chr5:128345803-128345804	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs200798627	chr5:128345891-128345892	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs577331303	chr5:128345913-128345914	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs181738905	chr5:128346001-128346002	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs546108717	chr5:128346003-128346004	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs556390195	chr5:128346097-128346098	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs576034456	chr5:128346112-128346113	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs7711249	chr5:128346137-128346138	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs7729201	chr5:128346144-128346145	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs184909746	chr5:128346169-128346170	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs541152550	chr5:128346197-128346198	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs560312464	chr5:128346208-128346209	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs139190851	chr5:128346246-128346247	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs552504245	chr5:128346269-128346270	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs569133254	chr5:128346280-128346281	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs377172891	chr5:128346330-128346331	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs531633747	chr5:128346368-128346369	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs538821013	chr5:128346369-128346370	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs548235863	chr5:128346430-128346431	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs144069334	chr5:128346458-128346459	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs528168308	chr5:128346497-128346498	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs533901125	chr5:128346507-128346508	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs541859720	chr5:128346588-128346589	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs370928216	chr5:128346602-128346603	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs145993830	chr5:128346605-128346606	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs571026042	chr5:128346610-128346611	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs189706959	chr5:128346696-128346697	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs77133936	chr5:128346707-128346708	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs180920441	chr5:128346708-128346709	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs552675126	chr5:128346735-128346736	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs139937994	chr5:128346746-128346747	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs373795517	chr5:128346752-128346753	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs542098442	chr5:128346792-128346793	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs184888491	chr5:128346812-128346813	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs115268313	chr5:128346819-128346820	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs541537456	chr5:128346847-128346848	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs530972499	chr5:128346861-128346862	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs190920891	chr5:128346950-128346951	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs532357173	chr5:128346981-128346982	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs547895970	chr5:128346990-128346991	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs550794211	chr5:128347064-128347065	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs571816944	chr5:128347174-128347175	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs570786873	chr5:128347180-128347181	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs182005424	chr5:128347200-128347201	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs142205190	chr5:128347232-128347233	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs79256642	chr5:128347262-128347263	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs554165457	chr5:128347263-128347264	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs568068060	chr5:128347268-128347269	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs367545768	chr5:128347309-128347310	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs186232818	chr5:128347323-128347324	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:77)

Disease	PMID	Source
Metanephric adenoma	20802469	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Cancer	16751803	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Cancer	22429812	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Liposarcoma	21253554	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Breast cancer	21858162	CNVD
Leukemia	17361228	CNVD
Myelodysplastic syndrome	18508791	CNVD
5q-syndrome	17576883	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	16740712	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Urothelial carcinoma	21177765	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
Lung cancer	18438408	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	CNVD
Squamous cell cancer	20885788	CNVD
Hepatocellular carcinoma	16750200	CNVD
Neurodevelopmental disorder	22521361	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	17133270	CNVD
Acute myeloid leukemia	20729466	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Cancer	20164920	CNVD
Myelodysplastic syndrome	21251322	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Multiple myeloma	17550852	CNVD
Colorectal cancer	16272173	CNVD
Salivary gland tumor	18059337	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Renal cell carcinoma	19377443	CNVD
Myelofibrosis	22110671	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Renal cell carcinoma	18194544	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Renal cell carcinoma	18592004	CNVD
small cell lung cancer	20016488	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:153 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:128329000-128372000	Weak transcription	Placenta Amnion	Placenta Amnion
2	chr5:128339200-128347000	Weak transcription	Fetal Heart	heart
3	chr5:128344400-128350200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr5:128344600-128347400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
5	chr5:128347000-128348200	Enhancers	Fetal Heart	heart
6	chr5:128347400-128349600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
7	chr5:128348200-128349800	Weak transcription	Fetal Heart	heart
8	chr5:128349600-128351000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
9	chr5:128349800-128350400	Genic enhancers	Fetal Heart	heart
10	chr5:128350200-128350400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
11	chr5:128350400-128350800	Enhancers	Fetal Heart	heart
12	chr5:128350800-128353400	Weak transcription	Fetal Heart	heart
13	chr5:128351000-128351200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
14	chr5:128351200-128352800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
15	chr5:128352800-128361400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
16	chr5:128353400-128355000	Genic enhancers	Fetal Heart	heart
17	chr5:128354600-128355400	Enhancers	Fetal Lung	lung
18	chr5:128354800-128355200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr5:128354800-128355200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
20	chr5:128354800-128355400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
21	chr5:128355000-128361400	Weak transcription	Fetal Heart	heart
22	chr5:128356600-128357400	Enhancers	Left Ventricle	heart
23	chr5:128356600-128357400	Enhancers	Right Ventricle	heart
24	chr5:128356600-128358600	Enhancers	Ovary	ovary
25	chr5:128357200-128357400	Enhancers	Fetal Lung	lung
26	chr5:128357200-128358600	Enhancers	Cortex derived primary cultured neurospheres	brain
27	chr5:128357400-128367200	Weak transcription	Right Ventricle	heart
28	chr5:128357400-128374000	Weak transcription	Left Ventricle	heart
29	chr5:128357600-128358200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
30	chr5:128357600-128358600	Enhancers	Brain Germinal Matrix	brain
31	chr5:128357800-128358000	Enhancers	Brain Substantia Nigra	brain
32	chr5:128358400-128358800	Enhancers	Brain Anterior Caudate	brain
33	chr5:128361400-128361600	Enhancers	Fetal Heart	heart
34	chr5:128361400-128368200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
35	chr5:128361600-128363200	Genic enhancers	Fetal Heart	heart
36	chr5:128363200-128366200	Weak transcription	Fetal Heart	heart
37	chr5:128366200-128367000	Strong transcription	Fetal Heart	heart
38	chr5:128367000-128379400	Weak transcription	Fetal Heart	heart
39	chr5:128368200-128370600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
40	chr5:128370600-128371600	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
41	chr5:128371600-128373600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
42	chr5:128373600-128374000	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
43	chr5:128374000-128374600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
44	chr5:128377200-128377600	Enhancers	Brain Germinal Matrix	brain
45	chr5:128377200-128377600	Enhancers	Colon Smooth Muscle	Colon
46	chr5:128377600-128378000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
47	chr5:128379400-128379800	Enhancers	Fetal Heart	heart
48	chr5:128379800-128383400	Weak transcription	Fetal Heart	heart
49	chr5:128381800-128390600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
50	chr5:128383400-128384600	Enhancers	Right Atrium	heart

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