Variant report

Variant	nsv1026912
Chromosome Location	chr8:5649416-5740359
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr8:5665134-5665329	H1-hESC	embryonic stem cell:	n/a	n/a
2	CEBPB	chr8:5731891-5732130	IMR90	lung:	n/a	chr8:5731971-5731982
3	CEBPB	chr8:5710994-5711190	HepG2	liver:	n/a	chr8:5711068-5711079
4	CEBPB	chr8:5731871-5732051	K562	blood:	n/a	chr8:5731971-5731982
5	CEBPB	chr8:5731829-5732132	H1-hESC	embryonic stem cell:	n/a	chr8:5731971-5731982
6	CEBPB	chr8:5665500-5665846	A549	lung:	n/a	chr8:5665672-5665685 chr8:5665674-5665683 chr8:5665672-5665683 chr8:5665674-5665683 chr8:5665576-5665584 chr8:5665672-5665685 chr8:5665674-5665683 chr8:5665674-5665683 chr8:5665673-5665684
7	CEBPB	chr8:5731799-5732146	HepG2	liver:	n/a	chr8:5731971-5731982
8	CEBPB	chr8:5664965-5665044	H1-hESC	embryonic stem cell:	n/a	n/a
9	CEBPB	chr8:5665512-5665799	K562	blood:	n/a	chr8:5665672-5665685 chr8:5665674-5665683 chr8:5665672-5665683 chr8:5665674-5665683 chr8:5665576-5665584 chr8:5665672-5665685 chr8:5665674-5665683 chr8:5665674-5665683 chr8:5665673-5665684
10	CEBPB	chr8:5665491-5665861	HepG2	liver:	n/a	chr8:5665672-5665685 chr8:5665674-5665683 chr8:5665672-5665683 chr8:5665674-5665683 chr8:5665576-5665584 chr8:5665672-5665685 chr8:5665674-5665683 chr8:5665674-5665683 chr8:5665673-5665684
11	CEBPB	chr8:5665505-5665860	IMR90	lung:	n/a	chr8:5665672-5665685 chr8:5665674-5665683 chr8:5665672-5665683 chr8:5665674-5665683 chr8:5665576-5665584 chr8:5665672-5665685 chr8:5665674-5665683 chr8:5665674-5665683 chr8:5665673-5665684
12	CEBPB	chr8:5665345-5665839	H1-hESC	embryonic stem cell:	n/a	chr8:5665672-5665685 chr8:5665674-5665683 chr8:5665672-5665683 chr8:5665674-5665683 chr8:5665576-5665584 chr8:5665672-5665685 chr8:5665674-5665683 chr8:5665674-5665683 chr8:5665673-5665684
13	CEBPB	chr8:5731815-5732103	A549	lung:	n/a	chr8:5731971-5731982
14	CTCF	chr8:5736007-5736188	LNCaP	prostate:	n/a	chr8:5736095-5736108
15	CTCF	chr8:5691640-5691790	HEK293	kidney:	n/a	n/a
16	CTCF	chr8:5657080-5657230	BE2_C	brain:	n/a	n/a
17	CTCF	chr8:5736051-5736137	MCF-7	breast:	n/a	chr8:5736095-5736108
18	CTCF	chr8:5657060-5657210	NB4	blood:	n/a	n/a
19	CTCF	chr8:5657148-5657214	GM12878	blood:	n/a	n/a
20	CTCF	chr8:5691640-5691790	WERI-Rb-1	eye:	n/a	n/a
21	CTCF	chr8:5691636-5691642	GM10248	blood:	n/a	n/a
22	CTCF	chr8:5657160-5657310	SK-N-SH_RA	brain:	n/a	n/a
23	CTCF	chr8:5657159-5657179	Hela-S3	cervix:	n/a	n/a
24	CTCF	chr8:5656980-5657130	NHEK	skin:	n/a	n/a
25	CTCF	chr8:5657060-5657210	BJ	skin:	n/a	n/a
26	CTCF	chr8:5736017-5736218	H1-hESC	embryonic stem cell:	n/a	chr8:5736095-5736108
27	CTCF	chr8:5730805-5730888	GM13976	blood:	n/a	n/a
28	CTCF	chr8:5740160-5740310	GM12869	blood:	n/a	n/a
29	CTCF	chr8:5736061-5736170	MCF-7	breast:	n/a	chr8:5736095-5736108
30	CTCF	chr8:5681765-5681786	GM13976	blood:	n/a	n/a
31	CTCF	chr8:5736027-5736169	MCF-7	breast:	n/a	chr8:5736095-5736108
32	CTCF	chr8:5738260-5738330	GM10266	blood:	n/a	n/a
33	CTCF	chr8:5657000-5657150	BE2_C	brain:	n/a	n/a
34	CTCF	chr8:5711303-5711369	Lung_OC	lung:	n/a	n/a
35	CTCF	chr8:5657120-5657270	GM12873	blood:	n/a	n/a
36	CTCF	chr8:5659516-5659560	LNCaP	prostate:	n/a	n/a
37	CTCF	chr8:5657080-5657230	GM12866	blood:	n/a	n/a
38	CTCF	chr8:5657000-5657150	Hela-S3	cervix:	n/a	n/a
39	CTCF	chr8:5736020-5736170	MCF-7	breast:	n/a	chr8:5736095-5736108
40	CTCF	chr8:5656980-5657130	A549	lung:	n/a	n/a
41	CTCF	chr8:5657106-5657167	Gliobla	brain:	n/a	n/a
42	CTCF	chr8:5736053-5736136	MCF-7	breast:	n/a	chr8:5736095-5736108
43	CTCF	chr8:5657040-5657190	HEK293	kidney:	n/a	n/a
44	CTCF	chr8:5691560-5691710	GM12871	blood:	n/a	n/a
45	CTCF	chr8:5650168-5650243	LNCaP	prostate:	n/a	n/a
46	CTCF	chr8:5736016-5736192	MCF-7	breast:	n/a	chr8:5736095-5736108
47	E2F4	chr8:5723929-5724173	MCF10A-Er-Src	breast:	n/a	n/a
48	E2F4	chr8:5654826-5655040	MCF10A-Er-Src	breast:	n/a	n/a
49	FAM48A	chr8:5674611-5674767	GM12878	blood:	n/a	n/a
50	FOS	chr8:5648823-5649426	MCF10A-Er-Src	breast:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr8:5653098..5655133-chr8:5666888..5669291,2	MCF-7	breast:
2	chr8:5658661..5661228-chr8:5666311..5668611,2	K562	blood:
3	chr8:5653098..5655133-chr8:5666888..5669291,2	MCF-7	breast:
4	chr8:5707497..5710127-chr8:5711033..5712692,2	K562	blood:
5	chr8:5658661..5661228-chr8:5666311..5668611,2	K562	blood:
6	chr8:5707497..5710127-chr8:5711033..5712692,2	K562	blood:
7	chr8:5655115..5656724-chr8:5659683..5662268,2	K562	blood:
8	chr8:5655115..5656724-chr8:5659683..5662268,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ANGPT2-13	chr8:5738563-5738710	l_3534_chr8:5703213-5738710_testes
2	lnc-ANGPT2-6	chr8:5715806-5715922	XLOC_006982
3	lnc-ANGPT2-13	chr8:5703214-5703330	l_3534_chr8:5703213-5738710_testes
4	lnc-MCPH1-4	chr8:5706219-5707214	NONHSAT124761

Variant related genes	Relation type
ENSG00000253571	TF binding region

Extended variants
information (count: 1947 )
Associated
traits (count: 130 )

Variant overlapped rSNPs/rCNVs (count:1947 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs554473564	chr8:5649417-5649418	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs572857299	chr8:5649418-5649419	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs376631097	chr8:5649434-5649435	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs1398489	chr8:5649451-5649452	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs188462513	chr8:5649463-5649464	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs147606458	chr8:5649469-5649470	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs181069582	chr8:5649478-5649479	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs551533247	chr8:5649484-5649485	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs531112940	chr8:5649507-5649508	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs1398488	chr8:5649551-5649552	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs186377362	chr8:5649555-5649556	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs528581386	chr8:5649571-5649572	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs112761290	chr8:5649604-5649605	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs190055821	chr8:5649607-5649608	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs544720475	chr8:5649621-5649622	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs28733480	chr8:5649622-5649623	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs569129082	chr8:5649629-5649630	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs142210434	chr8:5649671-5649672	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs572607692	chr8:5649676-5649677	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs369147290	chr8:5649706-5649707	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs554740742	chr8:5649715-5649716	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs566598110	chr8:5649721-5649722	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs200693557	chr8:5649770-5649771	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs151155590	chr8:5649797-5649798	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs558265000	chr8:5649802-5649803	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs114616448	chr8:5649822-5649823	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs543757311	chr8:5649842-5649843	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs555748271	chr8:5649879-5649880	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs547981538	chr8:5649880-5649881	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs542996278	chr8:5649883-5649884	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs561509114	chr8:5649885-5649886	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs528710789	chr8:5649891-5649892	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs10866996	chr8:5649893-5649894	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs565353125	chr8:5649911-5649912	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs117382531	chr8:5649913-5649914	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs181898822	chr8:5649940-5649941	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs11990941	chr8:5649986-5649987	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs530000779	chr8:5649987-5649988	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs548216295	chr8:5650010-5650011	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs566643964	chr8:5650037-5650038	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs143963672	chr8:5650044-5650045	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs187338967	chr8:5650054-5650055	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs9694510	chr8:5650076-5650077	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs537590105	chr8:5650081-5650082	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs60135765	chr8:5650119-5650120	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs574375582	chr8:5650144-5650145	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs536933657	chr8:5650165-5650166	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs145832139	chr8:5650171-5650172	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs376912088	chr8:5650176-5650177	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs573505452	chr8:5650180-5650181	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:130)

Disease	PMID	Source
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Prostate cancer	16573809	CNVD
Myelofibrosis	22110671	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
abnormal development	18461090	CNVD
Crohn''s disease	19220326	CNVD
Psoriasis	19220326	CNVD
Prostate cancer	21965145	CNVD
Prostate cancer	18515986	CNVD
Chronic obstructive pulmonary disease	20378733	CNVD
Autism	18414403	CNVD
Cancer	21183584	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Breast cancer	17603634	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Ovarian cancer	20844748	CNVD
Cervical cancer	17311676	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Schizophrenia	20877625	CNVD
Disorders of sex development	21048976	CNVD
Colorectal cancer	16272173	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Breast cancer	17001317	CNVD
Thyroid cancer	19087340	CNVD
Multiple myeloma	16616336	CNVD
Hepatocellular carcinoma	22174799	CNVD
Heart disease	21282601	CNVD
T-cell lymphomas	19863542	CNVD
Ovarian cancer	22174824	CNVD
Colorectal cancer	21297112	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Salivary gland tumor	18059337	CNVD
Breast cancer	17133270	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Breast cancer	17393978	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Breast cancer	20837533	CNVD
Squamous cell cancer	21044232	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	22429812	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Basal cell lymphoma	21115979	CNVD
Breast cancer	21264507	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Oral cancer	21386901	CNVD
Prostate cancer	21088497	CNVD
Breast cancer	20940404	CNVD
Colorectal cancer	19359472	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Gastric cancer	17167181	CNVD
Prostate cancer	16705090	CNVD
8p-syndrome	17576883	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
Lung adenocarcinoma	19525976	CNVD
Lung cancer	19525976	CNVD
Prostate cancer	17245344	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Cancer	16751803	CNVD
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Autism	19415332	CNVD
Malaria	21533027	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Esophageal cancer	21851588	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Breast cancer	21785460	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21509527	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Epilepsy	22083797	CNVD
Acute myeloid leukemia	21251322	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Autism	22495311	CNVD
Congenital diaphragmatic hernia	21064195	CNVD
Cancer	20164920	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Non-small cell lung cancer	21829676	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Prostate cancer	17217626	CNVD
Developmental delay	19128483	CNVD
Neuroticism	17667963	CNVD
Leukoplakia	24403051	CNVD
Intellectual disability	22045946	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	16608533	CNVD
Seminomas	18059402	CNVD
Breast cancer	21364760	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Colorectal cancer	16774939	CNVD
Lung squamous cell carcinoma	22363434	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Chronic myeloid leukemia	21384125	CNVD
Tetralogy of Fallot	22912587	CNVD
Type 2 diabetes	21526130	CNVD
Medulloblastoma	16783165	CNVD
early-passage human iPS cells	21368824	CNVD
Schizophrenia	20967226	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Schizophrenia	23813976	CNVD
Renal cell carcinoma	21215367	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:47 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:5648200-5654000	Enhancers	Dnd41	blood
2	chr8:5652000-5652600	Enhancers	Fetal Brain Female	brain
3	chr8:5652600-5653000	Enhancers	Fetal Brain Male	brain
4	chr8:5654000-5654200	Flanking Active TSS	Dnd41	blood
5	chr8:5654200-5656800	Enhancers	Dnd41	blood
6	chr8:5657400-5664000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
7	chr8:5660800-5661000	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
8	chr8:5661000-5664400	Weak transcription	H1 Cell Line	embryonic stem cell
9	chr8:5663400-5663600	Enhancers	H9 Cell Line	embryonic stem cell
10	chr8:5663400-5664800	Enhancers	iPS-20b Cell Line	embryonic stem cell
11	chr8:5664000-5664200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
12	chr8:5664000-5665000	Enhancers	HUES48 Cell Line	embryonic stem cell
13	chr8:5664000-5665600	Enhancers	iPS-15b Cell Line	embryonic stem cell
14	chr8:5664200-5664800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
15	chr8:5664400-5665000	Enhancers	ES-I3 Cell Line	embryonic stem cell
16	chr8:5664400-5665400	Enhancers	H1 Cell Line	embryonic stem cell
17	chr8:5664400-5665400	Enhancers	HUES64 Cell Line	embryonic stem cell
18	chr8:5664400-5665600	Enhancers	HUES6 Cell Line	embryonic stem cell
19	chr8:5664600-5666000	Enhancers	iPS-18 Cell Line	embryonic stem cell
20	chr8:5664800-5665000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
21	chr8:5664800-5665200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
22	chr8:5664800-5665400	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
23	chr8:5665000-5665400	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
24	chr8:5665000-5665400	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
25	chr8:5665000-5666600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
26	chr8:5665400-5665600	Enhancers	HUES48 Cell Line	embryonic stem cell
27	chr8:5665400-5665800	Enhancers	iPS-20b Cell Line	embryonic stem cell
28	chr8:5665400-5666400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
29	chr8:5665400-5666400	Weak transcription	H1 Cell Line	embryonic stem cell
30	chr8:5665400-5666400	Weak transcription	HUES64 Cell Line	embryonic stem cell
31	chr8:5665600-5666600	Weak transcription	HUES6 Cell Line	embryonic stem cell
32	chr8:5665600-5666600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
33	chr8:5665800-5666400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
34	chr8:5666000-5666400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
35	chr8:5666400-5667200	Enhancers	HUES64 Cell Line	embryonic stem cell
36	chr8:5666400-5667200	Enhancers	iPS-18 Cell Line	embryonic stem cell
37	chr8:5666400-5667200	Enhancers	iPS-20b Cell Line	embryonic stem cell
38	chr8:5666600-5666800	Enhancers	ES-I3 Cell Line	embryonic stem cell
39	chr8:5666600-5666800	Enhancers	H1 Cell Line	embryonic stem cell
40	chr8:5666600-5666800	Enhancers	HUES6 Cell Line	embryonic stem cell
41	chr8:5666600-5666800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
42	chr8:5666600-5667200	Enhancers	iPS-15b Cell Line	embryonic stem cell
43	chr8:5674400-5675400	Enhancers	Dnd41	blood
44	chr8:5687800-5688400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
45	chr8:5699600-5700000	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
46	chr8:5732800-5735400	Weak transcription	Fetal Heart	heart
47	chr8:5735400-5735600	Enhancers	Fetal Heart	heart

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