Variant report

Variant	nsv901833
Chromosome Location	chr14:44931593-45028731
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:201)
CpG islands
(count:122)
Chromatin interactive
region (count:15)
LncRNA
region (count:25)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:201 , 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	BCL11A	chr14:44974131-44974349	GM12878	blood:	n/a	n/a
2	CEBPB	chr14:44932945-44933181	Hela-S3	cervix:	n/a	n/a
3	CEBPB	chr14:44950479-44950667	A549	lung:	n/a	n/a
4	CEBPB	chr14:44979960-44980146	K562	blood:	n/a	n/a
5	CEBPB	chr14:44991866-44992131	HepG2	liver:	n/a	n/a
6	CEBPB	chr14:44957012-44957082	HepG2	liver:	n/a	chr14:44957022-44957033
7	CEBPB	chr14:44937997-44938297	A549	lung:	n/a	chr14:44938138-44938149 chr14:44938159-44938170
8	CEBPB	chr14:44937972-44938311	HepG2	liver:	n/a	chr14:44937995-44938006 chr14:44937995-44938008 chr14:44937995-44938008 chr14:44938138-44938149 chr14:44937995-44938008 chr14:44938159-44938170
9	CEBPB	chr14:44937993-44938273	Hela-S3	cervix:	n/a	chr14:44937995-44938006 chr14:44937995-44938008 chr14:44937995-44938008 chr14:44938138-44938149 chr14:44937995-44938008 chr14:44938159-44938170
10	CHD2	chr14:44979946-44980318	K562	blood:	n/a	n/a
11	CTCF	chr14:44974912-44975070	MCF-7	breast:	n/a	n/a
12	CTCF	chr14:44975060-44975210	HVMF	connective:	n/a	n/a
13	CTCF	chr14:44974960-44975110	HepG2	liver:	n/a	n/a
14	CTCF	chr14:44974908-44975076	MCF-7	breast:	n/a	n/a
15	CTCF	chr14:44974915-44975096	HepG2	liver:	n/a	n/a
16	CTCF	chr14:44948700-44948850	Hela-S3	cervix:	n/a	chr14:44948780-44948796
17	CTCF	chr14:44974880-44975030	K562	blood:	n/a	n/a
18	CTCF	chr14:44974940-44975090	GM12870	blood:	n/a	n/a
19	CTCF	chr14:44948724-44948816	HepG2	liver:	n/a	chr14:44948780-44948796
20	CTCF	chr14:44948700-44948850	MCF-7	breast:	n/a	chr14:44948780-44948796
21	CTCF	chr14:44974919-44975036	Pancreas_OC	pancreas:	n/a	n/a
22	CTCF	chr14:44974840-44974990	HL-60	blood:	n/a	n/a
23	CTCF	chr14:44998260-44998410	AoAF	blood vessel:	n/a	n/a
24	CTCF	chr14:44974960-44975110	HEK293	kidney:	n/a	n/a
25	CTCF	chr14:44974859-44975084	HepG2	liver:	n/a	n/a
26	CTCF	chr14:44948671-44948891	MCF-7	breast:	n/a	chr14:44948780-44948796
27	CTCF	chr14:44986742-44986802	Kidney_OC	kidney:	n/a	n/a
28	CTCF	chr14:44974900-44975050	MCF-7	breast:	n/a	n/a
29	CTCF	chr14:44974963-44975049	K562	blood:	n/a	n/a
30	CTCF	chr14:44974958-44975042	MCF-7	breast:	n/a	n/a
31	CTCF	chr14:44974940-44975049	H1-hESC	embryonic stem cell:	n/a	n/a
32	CTCF	chr14:44974874-44975172	MCF-7	breast:	n/a	n/a
33	CTCF	chr14:44974872-44975075	K562	blood:	n/a	n/a
34	CTCF	chr14:44974915-44975059	LNCaP	prostate:	n/a	n/a
35	CTCF	chr14:44985093-44985178	MCF-7	breast:	n/a	n/a
36	CTCF	chr14:44974860-44975010	GM12873	blood:	n/a	n/a
37	CTCF	chr14:44974860-44975010	Hela-S3	cervix:	n/a	n/a
38	CTCF	chr14:44974798-44975064	H1-hESC	embryonic stem cell:	n/a	n/a
39	CTCF	chr14:44974983-44975010	GM13977	blood:	n/a	n/a
40	CTCF	chr14:44974860-44975010	NB4	blood:	n/a	n/a
41	CTCF	chr14:44974800-44974950	A549	lung:	n/a	n/a
42	CTCF	chr14:44974878-44975104	MCF-7	breast:	n/a	n/a
43	CTCF	chr14:44948680-44948830	MCF-7	breast:	n/a	chr14:44948780-44948796
44	CTCF	chr14:44948693-44948868	MCF-7	breast:	n/a	chr14:44948780-44948796
45	CTCF	chr14:44975000-44975150	HCT-116	colon:	n/a	n/a
46	CTCF	chr14:44974916-44975071	MCF-7	breast:	n/a	n/a
47	CTCF	chr14:44974920-44975070	HepG2	liver:	n/a	n/a
48	CTCF	chr14:44974776-44975167	MCF-7	breast:	n/a	n/a
49	CTCF	chr14:44974780-44975076	HepG2	liver:	n/a	n/a
50	CTCF	chr14:44974940-44975090	HCT-116	colon:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:44976457-44976507	HEEpiC	esophagus:	n/a
2	chr14:44976233-44976283	HUVEC	blood vessel:	n/a
3	chr14:44976233-44976283	SK-N-MC	brain:	n/a
4	chr14:44976457-44976507	GM12891	blood:	n/a
5	chr14:44976233-44976283	ProgFib	skin:	n/a
6	chr14:44976457-44976507	NT2-D1	testis:	n/a
7	chr14:44976233-44976283	Hela-S3	cervix:	n/a
8	chr14:44976233-44976283	NHBE	bronchial:	n/a
9	chr14:44976457-44976507	NHDF-neo	bronchial:	n/a
10	chr14:44976457-44976507	CMK	blood:	n/a
11	chr14:44976233-44976283	AG04449	skin:	fetal
12	chr14:44976457-44976507	HRCEpiC	kidney:	n/a
13	chr14:44976457-44976507	AG04449	skin:	fetal
14	chr14:44976457-44976507	HCF	heart:	n/a
15	chr14:44976457-44976507	ECC-1	luminal epithelium:	n/a
16	chr14:44976457-44976507	A549	lung:	n/a
17	chr14:44976233-44976283	AG04450	lung:	fetal
18	chr14:44976457-44976507	BJ	skin:	n/a
19	chr14:44976233-44976283	U87	brain:	n/a
20	chr14:44976457-44976507	HPAEpiC	pulmonary alveolar:	n/a
21	chr14:44976233-44976283	HAEpiC	amniotic membrane:	n/a
22	chr14:44976457-44976507	SK-N-SH_RA	brain:	n/a
23	chr14:44976233-44976283	H1-hESC	embryonic stem cell:	embryo
24	chr14:44976457-44976507	HepG2	liver:	n/a
25	chr14:44976457-44976507	GM12878	blood:	n/a
26	chr14:44976457-44976507	ovcar-3	ovarian:	n/a
27	chr14:44976233-44976283	SAEC	small airway:	n/a
28	chr14:44976233-44976283	GM12892	blood:	n/a
29	chr14:44976233-44976283	PFSK-1	brain:	n/a
30	chr14:44976457-44976507	T-47D	breast:	n/a
31	chr14:44976457-44976507	ProgFib	skin:	n/a
32	chr14:44976233-44976283	HCF	heart:	n/a
33	chr14:44976233-44976283	HCT-116	colon:	n/a
34	chr14:44976233-44976283	MCF10A-Er-Src	breast:	n/a
35	chr14:44976233-44976283	HEEpiC	esophagus:	n/a
36	chr14:44976233-44976283	K562	blood:	n/a
37	chr14:44976457-44976507	HNPCEpiC	eye:	n/a
38	chr14:44976233-44976283	NHDF-neo	bronchial:	n/a
39	chr14:44976457-44976507	Hela-S3	cervix:	n/a
40	chr14:44976457-44976507	MCF10A-Er-Src	breast:	n/a
41	chr14:44976233-44976283	A549	lung:	n/a
42	chr14:44976457-44976507	Hepatocyte	liver:	n/a
43	chr14:44976233-44976283	HL-60	blood:	n/a
44	chr14:44976457-44976507	NHBE	bronchial:	n/a
45	chr14:44976233-44976283	GM19239	blood:	n/a
46	chr14:44976233-44976283	HCPEpiC	choroid plexus:	n/a
47	chr14:44976233-44976283	HepG2	liver:	n/a
48	chr14:44976457-44976507	HCPEpiC	choroid plexus:	n/a
49	chr14:44976457-44976507	GM19239	blood:	n/a
50	chr14:44976233-44976283	HRE	kidney:	n/a

(count:15 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:44838612..44839205-chr14:44974588..44975472,2	MCF-7	breast:
2	chr14:44972455..44975189-chr14:45002674..45004244,2	MCF-7	breast:
3	chr14:44980137..44981640-chr17:41380487..41382264,3	K562	blood:
4	chr1:17231477..17232007-chr14:44939008..44939528,2	Hela-S3	cervix:
5	chr14:44980118..44981638-chr17:41465259..41467724,2	MCF-7	breast:
6	chr14:44978619..44981639-chr17:41463816..41468065,6	K562	blood:
7	chr14:44980118..44981638-chr17:41380370..41382247,2	MCF-7	breast:
8	chr14:44980118..44981640-chr17:41398653..41402673,7	K562	blood:
9	chr14:44980119..44981639-chr17:41463633..41465366,4	MCF-7	breast:
10	chr14:44980119..44981640-chr17:41463656..41466583,4	K562	blood:
11	chr14:44980139..44981640-chr17:41398653..41400867,3	K562	blood:
12	chr14:44978638..44981619-chrX:77931842..77933343,2	K562	blood:
13	chr14:44948272..44949206-chr8:143706277..143707059,2	MCF-7	breast:
14	chr11:62607619..62609217-chr14:44980118..44981639,2	K562	blood:
15	chr14:44972455..44975189-chr14:45002674..45004244,2	MCF-7	breast:

(count:25 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FSCB-1	chr14:44949713-44949833	XLOC_011007
2	lnc-FSCB-1	chr14:44947932-44948054	ENSG00000258487
3	lnc-FSCB-1	chr14:44949713-44949821	ENSG00000258487
4	lnc-C14orf28-1	chr14:45007477-45007716	ENSG00000258747.1
5	lnc-FSCB-1	chr14:44949713-44949737	NONHSAT036608
6	lnc-C14orf28-1	chr14:44978530-44978686	ENSG00000258747.1
7	lnc-FSCB-1	chr14:44936293-44936372	XLOC_011007
8	lnc-FSCB-1	chr14:44947932-44948054	XLOC_011007
9	lnc-C14orf28-1	chr14:44976560-44976672	NONHSAT036614
10	lnc-FSCB-1	chr14:44947932-44948054	XLOC_011007
11	lnc-FSCB-1	chr14:44936161-44936372	ENSG00000258487
12	lnc-C14orf28-1	chr14:44976610-44976672	ENSG00000258747.1
13	lnc-C14orf28-1	chr14:44977855-44977932	NONHSAT036614
14	lnc-FSCB-1	chr14:44947923-44948054	ENSG00000258487
15	lnc-C14orf28-1	chr14:44978172-44978434	ENSG00000258747.1
16	lnc-C14orf28-1	chr14:44976612-44976672	ENSG00000258747.1
17	lnc-C14orf28-1	chr14:44977855-44977932	ENSG00000258747.1
18	lnc-FSCB-1	chr14:44949713-44949833	XLOC_011007
19	lnc-C14orf28-1	chr14:45007477-45007691	NONHSAT036614
20	lnc-FSCB-1	chr14:44949713-44949820	ENSG00000258487
21	lnc-C14orf28-1	chr14:45007477-45007714	ENSG00000258747.1
22	lnc-C14orf28-1	chr14:44978206-44978434	ENSG00000258747.1
23	lnc-FSCB-1	chr14:44947932-44948054	NONHSAT036608
24	lnc-FSCB-1	chr14:44947921-44948054	XLOC_011007
25	lnc-FSCB-1	chr14:44936162-44936372	XLOC_011007

No data

Variant related genes	Relation type
ENSG00000258747	TF binding region
FSCB	TF binding region
ENSG00000258487	TF binding region
ENSG00000258747	CpG island
FSCB	CpG island
ENSG00000258487	CpG island
ENSG00000188825	chromatin interactions
ENSG00000236383	chromatin interactions
ENSG00000133316	chromatin interactions

Extended variants
information (count: 1003 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:1003 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs527724134	chr14:44931625-44931626	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs34110674	chr14:44931645-44931646	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs116936807	chr14:44931651-44931652	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs147088453	chr14:44931652-44931653	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs147682244	chr14:44931680-44931681	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs568584926	chr14:44931734-44931735	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs34953921	chr14:44931755-44931756	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs1959373	chr14:44931802-44931803	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs77359051	chr14:44931814-44931815	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs143224412	chr14:44931853-44931854	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs539487518	chr14:44931858-44931859	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs368693123	chr14:44931859-44931860	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs188456636	chr14:44931946-44931947	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs569802749	chr14:44931986-44931987	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs415373	chr14:44932053-44932054	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs148293940	chr14:44932081-44932082	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs369778513	chr14:44932093-44932094	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs180949509	chr14:44932096-44932097	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs528689482	chr14:44932112-44932113	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs541209509	chr14:44932143-44932144	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs10145895	chr14:44932150-44932151	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs577490354	chr14:44932182-44932183	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs185944362	chr14:44932213-44932214	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs564153596	chr14:44932238-44932239	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs141433957	chr14:44932265-44932266	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs543515331	chr14:44932277-44932278	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs191993181	chr14:44932305-44932306	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs529506641	chr14:44932346-44932347	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs183859291	chr14:44932357-44932358	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs566271906	chr14:44932385-44932386	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs533652109	chr14:44932434-44932435	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs186421617	chr14:44932445-44932446	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs371659547	chr14:44932523-44932524	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs12432703	chr14:44932559-44932560	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs375096603	chr14:44932632-44932633	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs8012613	chr14:44932671-44932672	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs372923625	chr14:44932694-44932695	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs555211138	chr14:44932706-44932707	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs141697234	chr14:44932740-44932741	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs549393662	chr14:44932767-44932768	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs146246186	chr14:44932796-44932797	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs553114405	chr14:44932837-44932838	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs577380057	chr14:44932852-44932853	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs533133156	chr14:44932867-44932868	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs12436005	chr14:44932886-44932887	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs370790639	chr14:44932903-44932904	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs567023165	chr14:44932914-44932915	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs139163209	chr14:44932962-44932963	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs536363525	chr14:44936247-44936248	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
50	rs112698382	chr14:44936317-44936318	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a

Variant related diseases (count:58)

Disease	PMID	Source
Esophageal cancer	21851588	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
High-proliferative meningiomas	17937814	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21044232	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Medulloblastoma	21979893	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Hepatocellular carcinoma	22174799	CNVD
Colorectal cancer	16774939	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	17899364	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Chronic myeloid leukemia	20724749	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Wilms tumour	21544195	CNVD
Lung cancer	18438408	CNVD
Urothelial carcinoma	21177765	CNVD
Multiple myeloma	17550852	CNVD
Breast cancer	21785460	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	21858162	CNVD
Hirschsprung''s Disease	21712996	CNVD
Cancer	21183584	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Renal cell carcinoma	18194544	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21364760	CNVD
Melanoma	17363583	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:23 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:44931600-44932000	Enhancers	Fetal Muscle Leg	muscle
2	chr14:44932000-44932400	Weak transcription	Fetal Muscle Leg	muscle
3	chr14:44932400-44933000	Enhancers	Fetal Muscle Leg	muscle
4	chr14:44932600-44933000	Enhancers	Fetal Kidney	kidney
5	chr14:44937600-44938400	Enhancers	Fetal Intestine Large	intestine
6	chr14:44959400-44960000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr14:44960000-44960400	Enhancers	Brain Angular Gyrus	brain
8	chr14:44960000-44962400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr14:44977200-44977400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr14:44993600-44994200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr14:44994200-44995800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
12	chr14:44995800-45000400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr14:44997600-45001200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr14:44997800-44998800	Enhancers	Brain Substantia Nigra	brain
15	chr14:44997800-44999800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
16	chr14:44998000-44998400	Enhancers	Fetal Heart	heart
17	chr14:44998000-44998600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
18	chr14:44998200-44999000	Enhancers	NHDF-Ad	bronchial
19	chr14:44998200-44999200	Enhancers	Brain Hippocampus Middle	brain
20	chr14:44998400-44999000	Enhancers	Brain Cingulate Gyrus	brain
21	chr14:44998400-45004400	Weak transcription	Fetal Heart	heart
22	chr14:44998800-44999200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
23	chr14:45004400-45004600	Enhancers	Fetal Heart	heart

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