Variant report

Variant	nsv1029021
Chromosome Location	chr5:113551892-113599644
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:222)
CpG islands
(count:122)
Chromatin interactive
region (count:2)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:222 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr5:113573418-113573898	IMR90	lung:	n/a	n/a
2	CEBPB	chr5:113557574-113557819	HepG2	liver:	n/a	chr5:113557672-113557683
3	CEBPB	chr5:113574582-113574959	IMR90	lung:	n/a	chr5:113574757-113574770
4	CEBPB	chr5:113557513-113557859	IMR90	lung:	n/a	chr5:113557672-113557683
5	CEBPB	chr5:113578967-113579770	IMR90	lung:	n/a	n/a
6	CEBPB	chr5:113557558-113557747	A549	lung:	n/a	chr5:113557672-113557683
7	CTCF	chr5:113559740-113559890	HepG2	liver:	n/a	n/a
8	CTCF	chr5:113559732-113559881	K562	blood:	n/a	n/a
9	CTCF	chr5:113559655-113559922	SK-N-SH_RA	brain:	n/a	n/a
10	CTCF	chr5:113559700-113559850	GM12873	blood:	n/a	n/a
11	CTCF	chr5:113559620-113559770	A549	lung:	n/a	n/a
12	CTCF	chr5:113559680-113559830	HBMEC	blood vessel:	n/a	n/a
13	CTCF	chr5:113559800-113559950	HEEpiC	esophagus:	n/a	n/a
14	CTCF	chr5:113589300-113589450	WI-38	lung:	n/a	n/a
15	CTCF	chr5:113559660-113559810	GM12873	blood:	n/a	n/a
16	CTCF	chr5:113559513-113560053	A549	lung:	n/a	n/a
17	CTCF	chr5:113559600-113559750	HAc	cerebellar:	n/a	n/a
18	CTCF	chr5:113559740-113559890	HPAF	blood vessel:	n/a	n/a
19	CTCF	chr5:113559730-113559834	Kidney_OC	kidney:	n/a	n/a
20	CTCF	chr5:113559621-113559952	H1-hESC	embryonic stem cell:	n/a	n/a
21	CTCF	chr5:113559720-113559870	AG04450	lung:	n/a	n/a
22	CTCF	chr5:113559661-113559986	IMR90	lung:	n/a	n/a
23	CTCF	chr5:113559740-113559890	HA-sp	spinal cord:	n/a	n/a
24	CTCF	chr5:113559760-113559910	GM12867	blood:	n/a	n/a
25	CTCF	chr5:113559660-113559810	HAc	cerebellar:	n/a	n/a
26	CTCF	chr5:113559760-113559910	HVMF	connective:	n/a	n/a
27	CTCF	chr5:113559720-113559870	GM12865	blood:	n/a	n/a
28	CTCF	chr5:113559740-113559890	HRPEpiC	eye:	n/a	n/a
29	CTCF	chr5:113559760-113559910	HCPEpiC	choroid plexus:	n/a	n/a
30	CTCF	chr5:113559740-113559890	Hela-S3	cervix:	n/a	n/a
31	CTCF	chr5:113559780-113559930	AoAF	blood vessel:	n/a	n/a
32	CTCF	chr5:113559800-113559950	GM12871	blood:	n/a	n/a
33	CTCF	chr5:113559700-113559850	HMEC	breast:	n/a	n/a
34	CTCF	chr5:113559700-113559850	HEK293	kidney:	n/a	n/a
35	CTCF	chr5:113559760-113559910	HBMEC	blood vessel:	n/a	n/a
36	CTCF	chr5:113559673-113559957	K562	blood:	n/a	n/a
37	CTCF	chr5:113559780-113559930	MCF-7	breast:	n/a	n/a
38	CTCF	chr5:113559720-113559870	HCM	heart:	n/a	n/a
39	CTCF	chr5:113559740-113559890	HEEpiC	esophagus:	n/a	n/a
40	CTCF	chr5:113559760-113559910	HFF-Myc	foreskin:	n/a	n/a
41	CTCF	chr5:113559700-113559850	GM12866	blood:	n/a	n/a
42	CTCF	chr5:113559760-113559910	RPTEC	kidney:	n/a	n/a
43	CTCF	chr5:113559740-113559890	GM12869	blood:	n/a	n/a
44	CTCF	chr5:113559712-113559868	Hela-S3	cervix:	n/a	n/a
45	CTCF	chr5:113559680-113559830	GM12875	blood:	n/a	n/a
46	CTCF	chr5:113559684-113559906	GM13977	blood:	n/a	n/a
47	CTCF	chr5:113559760-113559910	HRPEpiC	eye:	n/a	n/a
48	CTCF	chr5:113559680-113559830	GM12870	blood:	n/a	n/a
49	CTCF	chr5:113559720-113559870	HCT-116	colon:	n/a	n/a
50	CTCF	chr5:113576147-113576172	LNCaP	prostate:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:113589213-113589263	PFSK-1	brain:	n/a
2	chr5:113590940-113590990	ovcar-3	ovarian:	n/a
3	chr5:113589213-113589263	HL-60	blood:	n/a
4	chr5:113589213-113589263	Caco-2	colon:	n/a
5	chr5:113589213-113589263	U87	brain:	n/a
6	chr5:113589213-113589263	HRE	kidney:	n/a
7	chr5:113590940-113590990	NH-A	brain:	n/a
8	chr5:113589213-113589263	T-47D	breast:	n/a
9	chr5:113589213-113589263	HEK293	kidney:	embryo
10	chr5:113589213-113589263	NH-A	brain:	n/a
11	chr5:113590940-113590990	SAEC	small airway:	n/a
12	chr5:113590940-113590990	SKMC	muscle:	n/a
13	chr5:113589213-113589263	K562	blood:	n/a
14	chr5:113589213-113589263	Hepatocyte	liver:	n/a
15	chr5:113589213-113589263	CMK	blood:	n/a
16	chr5:113590940-113590990	GM19239	blood:	n/a
17	chr5:113589213-113589263	HPAEpiC	pulmonary alveolar:	n/a
18	chr5:113589213-113589263	MCF10A-Er-Src	breast:	n/a
19	chr5:113589213-113589263	HRPEpiC	eye:	n/a
20	chr5:113589213-113589263	NHDF-neo	bronchial:	n/a
21	chr5:113589213-113589263	HIPEpiC	eye:	n/a
22	chr5:113590940-113590990	Jurkat	blood:	n/a
23	chr5:113590940-113590990	HNPCEpiC	eye:	n/a
24	chr5:113589213-113589263	HUVEC	blood vessel:	n/a
25	chr5:113590940-113590990	LNCaP	prostate:	n/a
26	chr5:113590940-113590990	HRE	kidney:	n/a
27	chr5:113589213-113589263	ProgFib	skin:	n/a
28	chr5:113589213-113589263	AG04449	skin:	fetal
29	chr5:113590940-113590990	SK-N-SH	brain:	n/a
30	chr5:113589213-113589263	HCM	heart:	n/a
31	chr5:113590940-113590990	NHBE	bronchial:	n/a
32	chr5:113589213-113589263	SK-N-MC	brain:	n/a
33	chr5:113589213-113589263	SK-N-SH	brain:	n/a
34	chr5:113590940-113590990	HCT-116	colon:	n/a
35	chr5:113589213-113589263	RPTEC	kidney:	n/a
36	chr5:113590940-113590990	HL-60	blood:	n/a
37	chr5:113589213-113589263	BJ	skin:	n/a
38	chr5:113589213-113589263	A549	lung:	n/a
39	chr5:113589213-113589263	HRCEpiC	kidney:	n/a
40	chr5:113589213-113589263	HCT-116	colon:	n/a
41	chr5:113590940-113590990	Caco-2	colon:	n/a
42	chr5:113590940-113590990	BE2_C	brain:	n/a
43	chr5:113590940-113590990	MCF10A-Er-Src	breast:	n/a
44	chr5:113590940-113590990	AG04449	skin:	fetal
45	chr5:113590940-113590990	HRCEpiC	kidney:	n/a
46	chr5:113589213-113589263	Jurkat	blood:	n/a
47	chr5:113590940-113590990	BJ	skin:	n/a
48	chr5:113589213-113589263	Hela-S3	cervix:	n/a
49	chr5:113590940-113590990	HRPEpiC	eye:	n/a
50	chr5:113589213-113589263	HCPEpiC	choroid plexus:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr5:113589881..113591473-chr5:113600185..113602176,2	K562	blood:
2	chr5:113583124..113585707-chr5:113637136..113639363,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KCNN2-4	chr5:113585076-113585161	l_2997_chr5:113419571-113469367_heart
2	lnc-KCNN2-3	chr5:113589210-113589451	NONHSAT103278

No data

Variant related genes	Relation type
RN7SKP89	TF binding region
RN7SKP89	CpG island

Extended variants
information (count: 1371 )
Associated
traits (count: 79 )

Variant overlapped rSNPs/rCNVs (count:1371 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs544953998	chr5:113554620-113554621	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs4572991	chr5:113554634-113554635	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs563035771	chr5:113554640-113554641	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs4521461	chr5:113554704-113554705	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs4624786	chr5:113554739-113554740	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs78598680	chr5:113554744-113554745	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs551449143	chr5:113554765-113554766	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs528424636	chr5:113554782-113554783	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs546701031	chr5:113554803-113554804	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs568208940	chr5:113554814-113554815	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs189568013	chr5:113554843-113554844	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs550733268	chr5:113554861-113554862	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs566572136	chr5:113554876-113554877	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs544056474	chr5:113554919-113554920	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs568922424	chr5:113554975-113554976	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs13186297	chr5:113554976-113554977	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs557719317	chr5:113554989-113554990	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs566482539	chr5:113555024-113555025	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs548961237	chr5:113555041-113555042	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs533760109	chr5:113555123-113555124	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs6892162	chr5:113555128-113555129	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs537734907	chr5:113555154-113555155	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs535704911	chr5:113555158-113555159	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs538624269	chr5:113555164-113555165	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs556056467	chr5:113555210-113555211	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs182763626	chr5:113555215-113555216	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs575723105	chr5:113555253-113555254	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs186058466	chr5:113555257-113555258	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs191406726	chr5:113555265-113555266	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs141478362	chr5:113555330-113555331	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs79061792	chr5:113555358-113555359	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs538453256	chr5:113555376-113555377	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs72797678	chr5:113555377-113555378	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs573281374	chr5:113555388-113555389	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs183168641	chr5:113555394-113555395	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs550767152	chr5:113555395-113555396	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs112642983	chr5:113555407-113555408	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs376467564	chr5:113555412-113555413	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs146291300	chr5:113555425-113555426	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs202245782	chr5:113555492-113555493	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs4074169	chr5:113555571-113555572	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs544892327	chr5:113555591-113555592	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs551694313	chr5:113555603-113555604	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs75104002	chr5:113555616-113555617	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs4537054	chr5:113555626-113555627	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs187382499	chr5:113555669-113555670	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs192165750	chr5:113555715-113555716	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs537968653	chr5:113555770-113555771	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs561648448	chr5:113555798-113555799	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs527476336	chr5:113555800-113555801	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:79)

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
Breast cancer	17393978	CNVD
Cancer	21359685	CNVD
Non-small cell lung cancer	21829676	CNVD
adenomatous polyposis	22470819	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
Retinoblastoma	22278416	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
Colorectal cancer	16774939	CNVD
Colorectal cancer	16272173	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Multiple myeloma	17550852	CNVD
Ovarian cancer	21720365	CNVD
Neurocytoma	17123091	CNVD
Salivary gland tumor	18059337	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Renal cell carcinoma	19377443	CNVD
Colorectal cancer	21297112	CNVD
Prostate cancer	16461572	CNVD
Myelofibrosis	22110671	CNVD
Sezary syndrome	18413736	CNVD
Autism	22495309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:91 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:113554600-113555200	Enhancers	Left Ventricle	heart
2	chr5:113555200-113561600	Weak transcription	Left Ventricle	heart
3	chr5:113558000-113558800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
4	chr5:113558800-113559400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
5	chr5:113559400-113559600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
6	chr5:113559400-113559800	Enhancers	HUVEC	blood vessel
7	chr5:113573000-113573600	Enhancers	Primary hematopoietic stem cells short term culture	blood
8	chr5:113573600-113574600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
9	chr5:113573600-113575000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chr5:113574200-113575000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
11	chr5:113574400-113575000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
12	chr5:113574600-113574800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
13	chr5:113574600-113575200	Enhancers	Primary hematopoietic stem cells short term culture	blood
14	chr5:113574800-113579000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
15	chr5:113575000-113577600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
16	chr5:113575200-113579400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
17	chr5:113577000-113579400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
18	chr5:113577600-113578000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
19	chr5:113578000-113579000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
20	chr5:113578800-113579000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
21	chr5:113578800-113579000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
22	chr5:113579000-113579200	Flanking Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
23	chr5:113579000-113579200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
24	chr5:113579000-113579400	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
25	chr5:113579000-113579400	Enhancers	NH-A	brain
26	chr5:113579000-113579600	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
27	chr5:113579000-113579600	Active TSS	Stomach Smooth Muscle	stomach
28	chr5:113579200-113579400	Enhancers	Fetal Heart	heart
29	chr5:113579200-113579600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
30	chr5:113579200-113579800	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
31	chr5:113579200-113579800	Enhancers	Muscle Satellite Cultured Cells	--
32	chr5:113579400-113579800	Enhancers	Primary hematopoietic stem cells short term culture	blood
33	chr5:113579400-113580000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
34	chr5:113579400-113581400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
35	chr5:113579400-113585600	Weak transcription	Fetal Heart	heart
36	chr5:113579600-113579800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
37	chr5:113579600-113580000	Active TSS	NH-A	brain
38	chr5:113579600-113580600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
39	chr5:113579800-113580000	Flanking Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
40	chr5:113580000-113581600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
41	chr5:113580600-113581400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
42	chr5:113581400-113581600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
43	chr5:113581400-113585800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
44	chr5:113581600-113584600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
45	chr5:113581600-113586000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
46	chr5:113584600-113586600	Enhancers	Fetal Stomach	stomach
47	chr5:113584600-113587200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
48	chr5:113585600-113586200	Enhancers	Fetal Lung	lung
49	chr5:113585600-113586200	Enhancers	NHDF-Ad	bronchial
50	chr5:113585600-113587000	Enhancers	Fetal Heart	heart

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