Variant report

Variant	nsv831616
Chromosome Location	chr9:73077855-73220928
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2006)
CpG islands
(count:366)
Chromatin interactive
region (count:119)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2006 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:73098204-73098455	K562	blood:	n/a	n/a
2	ARID3A	chr9:73217378-73217685	K562	blood:	n/a	n/a
3	ARID3A	chr9:73099994-73100983	K562	blood:	n/a	n/a
4	ARID3A	chr9:73085191-73086064	HepG2	liver:	n/a	n/a
5	ARID3A	chr9:73089498-73089696	HepG2	liver:	n/a	n/a
6	ARID3A	chr9:73095326-73095569	HepG2	liver:	n/a	n/a
7	ARID3A	chr9:73116474-73116704	K562	blood:	n/a	n/a
8	ARID3A	chr9:73099207-73099753	K562	blood:	n/a	n/a
9	ARID3A	chr9:73217429-73217695	HepG2	liver:	n/a	n/a
10	ATF1	chr9:73099214-73100595	K562	blood:	n/a	n/a
11	ATF1	chr9:73192401-73192592	K562	blood:	n/a	n/a
12	ATF2	chr9:73178271-73179139	GM12878	blood:	n/a	n/a
13	ATF2	chr9:73178465-73179115	GM12878	blood:	n/a	n/a
14	ATF3	chr9:73085372-73085610	HepG2	liver:	n/a	n/a
15	ATF3	chr9:73100198-73100587	K562	blood:	n/a	n/a
16	BACH1	chr9:73100290-73100639	K562	blood:	n/a	n/a
17	BATF	chr9:73134896-73135266	GM12878	blood:	n/a	n/a
18	BATF	chr9:73178230-73179035	GM12878	blood:	n/a	n/a
19	BATF	chr9:73134867-73135477	GM12878	blood:	n/a	n/a
20	BATF	chr9:73178395-73179000	GM12878	blood:	n/a	n/a
21	BCL11A	chr9:73178438-73179003	GM12878	blood:	n/a	n/a
22	BCL11A	chr9:73134930-73135267	GM12878	blood:	n/a	n/a
23	BCL11A	chr9:73178555-73179007	GM12878	blood:	n/a	n/a
24	BCL11A	chr9:73134998-73135247	GM12878	blood:	n/a	n/a
25	BCL11A	chr9:73173126-73173370	GM12878	blood:	n/a	n/a
26	BCLAF1	chr9:73178520-73179034	GM12878	blood:	n/a	n/a
27	BHLHE40	chr9:73178513-73179011	GM12878	blood:	n/a	n/a
28	BHLHE40	chr9:73202411-73202445	K562	blood:	n/a	n/a
29	BHLHE40	chr9:73217351-73217636	K562	blood:	n/a	n/a
30	BHLHE40	chr9:73090205-73090465	K562	blood:	n/a	n/a
31	BHLHE40	chr9:73085293-73085894	HepG2	liver:	n/a	n/a
32	BHLHE40	chr9:73192220-73192606	K562	blood:	n/a	n/a
33	BHLHE40	chr9:73215987-73216302	K562	blood:	n/a	n/a
34	BHLHE40	chr9:73100015-73100636	K562	blood:	n/a	n/a
35	BRCA1	chr9:73186849-73186861	Hela-S3	cervix:	n/a	n/a
36	BRCA1	chr9:73107915-73107950	GM12878	blood:	n/a	n/a
37	BRCA1	chr9:73217428-73217711	H1-hESC	embryonic stem cell:	n/a	n/a
38	BRCA1	chr9:73125171-73125353	H1-hESC	embryonic stem cell:	n/a	n/a
39	CBX3	chr9:73100139-73100654	K562	blood:	n/a	n/a
40	CCNT2	chr9:73100098-73100648	K562	blood:	n/a	chr9:73100335-73100355 chr9:73100424-73100444
41	CCNT2	chr9:73129202-73129521	K562	blood:	n/a	n/a
42	CEBPB	chr9:73109707-73109942	IMR90	lung:	n/a	chr9:73109816-73109827
43	CEBPB	chr9:73189328-73189805	IMR90	lung:	n/a	n/a
44	CEBPB	chr9:73183571-73183602	HepG2	liver:	n/a	chr9:73183574-73183585
45	CEBPB	chr9:73176640-73177103	IMR90	lung:	n/a	n/a
46	CEBPB	chr9:73149091-73149267	Hela-S3	cervix:	n/a	n/a
47	CEBPB	chr9:73105732-73105801	K562	blood:	n/a	n/a
48	CEBPB	chr9:73093915-73094203	IMR90	lung:	n/a	n/a
49	CEBPB	chr9:73217334-73217792	H1-hESC	embryonic stem cell:	n/a	n/a
50	CEBPB	chr9:73100054-73100876	K562	blood:	n/a	n/a

(count:366 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:73148415-73148465	AG04449	skin:	fetal
2	chr9:73095740-73095790	HepG2	liver:	n/a
3	chr9:73103756-73103806	HIPEpiC	eye:	n/a
4	chr9:73178360-73178410	SAEC	small airway:	n/a
5	chr9:73148415-73148465	Jurkat	blood:	n/a
6	chr9:73103756-73103806	HAEpiC	amniotic membrane:	n/a
7	chr9:73103756-73103806	Caco-2	colon:	n/a
8	chr9:73148415-73148465	HCM	heart:	n/a
9	chr9:73103756-73103806	SKMC	muscle:	n/a
10	chr9:73095740-73095790	AG09319	gingival:	n/a
11	chr9:73189590-73189640	NH-A	brain:	n/a
12	chr9:73095740-73095790	AG04450	lung:	fetal
13	chr9:73152198-73152248	HCM	heart:	n/a
14	chr9:73189590-73189640	GM19239	blood:	n/a
15	chr9:73103756-73103806	HCF	heart:	n/a
16	chr9:73178360-73178410	ovcar-3	ovarian:	n/a
17	chr9:73103756-73103806	AG09309	skin:	n/a
18	chr9:73095740-73095790	HRE	kidney:	n/a
19	chr9:73152198-73152248	HNPCEpiC	eye:	n/a
20	chr9:73148415-73148465	RPTEC	kidney:	n/a
21	chr9:73095740-73095790	HAEpiC	amniotic membrane:	n/a
22	chr9:73148415-73148465	HPAEpiC	pulmonary alveolar:	n/a
23	chr9:73178360-73178410	HIPEpiC	eye:	n/a
24	chr9:73103756-73103806	ECC-1	luminal epithelium:	n/a
25	chr9:73152198-73152248	GM12892	blood:	n/a
26	chr9:73095740-73095790	HCPEpiC	choroid plexus:	n/a
27	chr9:73189590-73189640	HCM	heart:	n/a
28	chr9:73189590-73189640	PANC-1	pancreas:	n/a
29	chr9:73178360-73178410	NH-A	brain:	n/a
30	chr9:73178360-73178410	PFSK-1	brain:	n/a
31	chr9:73189590-73189640	ProgFib	skin:	n/a
32	chr9:73152198-73152248	Hepatocyte	liver:	n/a
33	chr9:73189590-73189640	HPAEpiC	pulmonary alveolar:	n/a
34	chr9:73178360-73178410	H1-hESC	embryonic stem cell:	embryo
35	chr9:73189590-73189640	AG10803	skin:	n/a
36	chr9:73148415-73148465	MCF10A-Er-Src	breast:	n/a
37	chr9:73148415-73148465	HCPEpiC	choroid plexus:	n/a
38	chr9:73152198-73152248	PrEC	prostate:	n/a
39	chr9:73189590-73189640	SK-N-SH	brain:	n/a
40	chr9:73189590-73189640	HepG2	liver:	n/a
41	chr9:73189590-73189640	HCT-116	colon:	n/a
42	chr9:73152198-73152248	AoSMC	blood vessel:	n/a
43	chr9:73148415-73148465	NT2-D1	testis:	n/a
44	chr9:73148415-73148465	BJ	skin:	n/a
45	chr9:73103756-73103806	ProgFib	skin:	n/a
46	chr9:73189590-73189640	CMK	blood:	n/a
47	chr9:73189590-73189640	AG09319	gingival:	n/a
48	chr9:73148415-73148465	ovcar-3	ovarian:	n/a
49	chr9:73152198-73152248	HRPEpiC	eye:	n/a
50	chr9:73178360-73178410	CMK	blood:	n/a

(count:119 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr3:112280225..112280976-chr9:73090788..73091346,2	HCT-116	colon:
2	chr9:73081016..73082623-chr9:73085751..73087573,2	K562	blood:
3	chr9:73170241..73173099-chr9:73173293..73176784,3	K562	blood:
4	chr9:73034153..73036328-chr9:73114890..73117338,2	K562	blood:
5	chr9:73033892..73035832-chr9:73188677..73192250,3	MCF-7	breast:
6	chr9:73182202..73183987-chr9:73186312..73187958,2	K562	blood:
7	chr9:73028709..73030401-chr9:73125089..73126791,2	K562	blood:
8	chr9:73028203..73029988-chr9:73203454..73205453,2	MCF-7	breast:
9	chr9:73021797..73024342-chr9:73098392..73100733,2	MCF-7	breast:
10	chr9:73197794..73199426-chr9:73200982..73203478,2	K562	blood:
11	chr9:73135819..73137820-chr9:73148526..73151153,2	K562	blood:
12	chr9:73094287..73096782-chr9:73098912..73101911,3	K562	blood:
13	chr9:73147901..73149420-chr9:73158466..73161054,2	K562	blood:
14	chr9:73098006..73100927-chr9:73106151..73108210,2	MCF-7	breast:
15	chr9:73106041..73107719-chr9:73109475..73112374,2	K562	blood:
16	chr9:73025336..73030126-chr9:73090773..73099381,13	MCF-7	breast:
17	chr9:73034438..73037233-chr9:73161780..73164205,2	MCF-7	breast:
18	chr9:73023259..73025640-chr9:73098632..73100320,2	K562	blood:
19	chr9:73089437..73091298-chr9:73095044..73096704,2	K562	blood:
20	chr9:73085757..73088696-chr9:73091890..73094537,4	K562	blood:
21	chr9:73030963..73039331-chr9:73089885..73101071,36	MCF-7	breast:
22	chr9:73117787..73119744-chr9:73123664..73126320,2	K562	blood:
23	chr9:73033648..73035671-chr9:73107577..73110365,3	MCF-7	breast:
24	chr9:73170241..73173099-chr9:73173293..73176784,3	K562	blood:
25	chr9:73034292..73034892-chr9:73092889..73093573,2	MCF-7	breast:
26	chr9:73207124..73209818-chr9:73212763..73214448,2	K562	blood:
27	chr9:73026175..73028721-chr9:73217630..73219674,2	K562	blood:
28	chr9:73028345..73030685-chr9:73109047..73111392,2	K562	blood:
29	chr9:72955229..72956123-chr9:73099181..73099956,4	K562	blood:
30	chr9:73034390..73036062-chr9:73122799..73124720,2	MCF-7	breast:
31	chr9:72967533..72968221-chr9:73217175..73217782,2	MCF-7	breast:
32	chr9:72955484..72956149-chr9:73217043..73217606,2	MCF-7	breast:
33	chr9:73216054..73218169-chr9:73220348..73222412,2	MCF-7	breast:
34	chr9:73036403..73038506-chr9:73197220..73199887,2	MCF-7	breast:
35	chr9:73032761..73036608-chr9:73073502..73079419,5	K562	blood:
36	chr9:72955339..72956157-chr9:73216775..73218041,5	K562	blood:
37	chr9:73035839..73037455-chr9:73087792..73090364,2	MCF-7	breast:
38	chr9:73025505..73030167-chr9:73091131..73097285,11	MCF-7	breast:
39	chr9:73147901..73149420-chr9:73158466..73161054,2	K562	blood:
40	chr9:73093971..73096517-chr9:73098061..73099840,2	MCF-7	breast:
41	chr9:73102768..73104960-chr9:73107078..73109058,2	K562	blood:
42	chr9:73216054..73218169-chr9:73220348..73222412,2	MCF-7	breast:
43	chr9:73168541..73170493-chr9:73179551..73181624,2	MCF-7	breast:
44	chr9:73197703..73200257-chr9:73201325..73204696,3	MCF-7	breast:
45	chr9:72586975..72587497-chr9:73124835..73125760,2	K562	blood:
46	chr9:73130256..73133199-chr9:73140433..73142212,2	K562	blood:
47	chr9:73032264..73037880-chr9:73093717..73104954,17	K562	blood:
48	chr9:72978429..72981216-chr9:73204901..73207733,2	MCF-7	breast:
49	chr9:73123988..73126460-chr9:73126959..73128717,2	MCF-7	breast:
50	chr9:73089437..73091298-chr9:73095044..73096704,2	K562	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SMC5-9	chr9:73218282-73218592	NONHSAT131818
2	lnc-SMC5-8	chr9:73145108-73145496	NONHSAT131817
3	lnc-SMC5-8	chr9:73143977-73144532	NONHSAT131817
4	lnc-SMC5-9	chr9:73216899-73217010	NONHSAT131818

No data

Variant related genes	Relation type
ENSG00000272232	TF binding region
ENSG00000272232	CpG island
ENSG00000272232	chromatin interactions
ENSG00000144848	chromatin interactions
ENSG00000119138	chromatin interactions
ENSG00000138459	chromatin interactions

Extended variants
information (count: 5441 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:5441 , 50 per page) page: 1 2 3 4 5 6 7 ... 109

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs183420471	chr9:73077886-73077887	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs75804185	chr9:73077894-73077895	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs138193328	chr9:73078027-73078028	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs566904870	chr9:73078037-73078038	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs531255619	chr9:73078101-73078102	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs146664663	chr9:73078160-73078161	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs548958420	chr9:73078162-73078163	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs372355292	chr9:73078168-73078169	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs569462302	chr9:73078194-73078195	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs535762951	chr9:73078236-73078237	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs112584060	chr9:73078252-73078253	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs186377047	chr9:73078335-73078336	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs552617345	chr9:73078422-73078423	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs138742984	chr9:73078424-73078425	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs12349372	chr9:73078429-73078430	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs112090733	chr9:73078464-73078465	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs368128768	chr9:73078561-73078562	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs534272254	chr9:73078570-73078571	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs555926331	chr9:73078588-73078589	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs534942002	chr9:73078594-73078595	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs145413448	chr9:73078595-73078596	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs574079445	chr9:73078692-73078693	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs116307995	chr9:73078694-73078695	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs373865505	chr9:73078749-73078750	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs556382296	chr9:73078790-73078791	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs12341550	chr9:73078826-73078827	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs545158365	chr9:73078849-73078850	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs190840771	chr9:73078864-73078865	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs142732275	chr9:73078869-73078870	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs368300330	chr9:73078953-73078954	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs532912909	chr9:73079017-73079018	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs182276129	chr9:73079045-73079046	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs147360593	chr9:73079066-73079067	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs137880565	chr9:73079094-73079095	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs563169699	chr9:73079103-73079104	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs368214675	chr9:73079131-73079132	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs112813792	chr9:73079156-73079157	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs78225628	chr9:73079171-73079172	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs77385354	chr9:73079211-73079212	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs534441613	chr9:73079242-73079243	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs372057207	chr9:73079243-73079244	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs567769606	chr9:73079285-73079286	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs200088722	chr9:73079293-73079294	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs149547836	chr9:73079309-73079310	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs144156199	chr9:73079314-73079315	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs115611140	chr9:73079328-73079329	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs538538495	chr9:73079379-73079380	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs148678723	chr9:73079415-73079416	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs571904302	chr9:73079424-73079425	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs187622560	chr9:73079435-73079436	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:68)

Disease	PMID	Source
Breast cancer	17133270	CNVD
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
Renal cell carcinoma	18592004	CNVD
Developmental delay	19490664	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Medulloblastoma	21979893	CNVD
microdeletion syndrome	16199537	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
Urothelial carcinoma	21177765	CNVD
Renal cell carcinoma	21668985	CNVD
Autism	22495311	CNVD
Melanoma	18172304	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Melanoma	22183965	CNVD
Cancer	16751803	CNVD
Myelofibrosis	22110671	CNVD
lymphocytic leukemia	21291569	CNVD
Leukemia	17361228	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Glioblastoma	16823260	CNVD
Leukemia	18688285	CNVD
Non-small cell lung cancer	21044232	CNVD
Brain cancer	20823417	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Renal cell carcinoma	19461508	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Heart disease	21282601	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute myeloid leukemia	21251322	CNVD
Hepatocellular carcinoma	16750200	CNVD
Acute myeloid leukemia	20729466	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Oral cancer	21386901	CNVD
Epilepsy	22083797	CNVD
Glioblastoma multiforme	21750150	CNVD
Cancer	21183584	CNVD
Bipolar disorder	18458673	CNVD
Breast cancer	22522925	CNVD
Intellectual disability	21811512	CNVD
Autism	21484199	CNVD
Breast cancer	22737080	CNVD
Malignant peripheral nerve sheath tumor	22811580	CNVD
Leprosy	22719964	CNVD
Primary ovarian insufficiency	22879975	CNVD
Malignant melanoma	17260012	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Schizophrenia	23813976	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:2448 , 50 per page) page: 1 2 3 4 5 6 7 ... 49

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:73067600-73080400	Weak transcription	Skeletal Muscle Male	skeletal muscle
2	chr9:73071400-73078600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
3	chr9:73071400-73081800	Weak transcription	Lung	lung
4	chr9:73071600-73082200	Weak transcription	Pancreas	Pancrea
5	chr9:73072400-73084800	Weak transcription	Sigmoid Colon	Sigmoid Colon
6	chr9:73075600-73078600	Weak transcription	Right Atrium	heart
7	chr9:73076800-73078200	Enhancers	Psoas Muscle	Psoas
8	chr9:73077000-73079200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
9	chr9:73077400-73078600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
10	chr9:73077600-73078600	Weak transcription	Muscle Satellite Cultured Cells	--
11	chr9:73077600-73078600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
12	chr9:73077600-73080400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
13	chr9:73077600-73080400	Weak transcription	Skeletal Muscle Female	skeletal muscle
14	chr9:73077600-73087800	Weak transcription	Gastric	stomach
15	chr9:73078200-73078600	Weak transcription	Psoas Muscle	Psoas
16	chr9:73078200-73078600	Weak transcription	Right Ventricle	heart
17	chr9:73078200-73082200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
18	chr9:73078400-73078800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
19	chr9:73078600-73078800	Enhancers	Psoas Muscle	Psoas
20	chr9:73078600-73078800	Enhancers	Right Atrium	heart
21	chr9:73078600-73078800	Enhancers	Right Ventricle	heart
22	chr9:73078600-73079000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
23	chr9:73078600-73079200	Enhancers	Muscle Satellite Cultured Cells	--
24	chr9:73078600-73079200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
25	chr9:73078600-73079400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
26	chr9:73078800-73079000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
27	chr9:73078800-73080400	Weak transcription	Psoas Muscle	Psoas
28	chr9:73078800-73080400	Weak transcription	Right Atrium	heart
29	chr9:73078800-73080400	Weak transcription	Right Ventricle	heart
30	chr9:73079000-73081400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
31	chr9:73079200-73080400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr9:73079200-73080400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
33	chr9:73079200-73081200	Weak transcription	Muscle Satellite Cultured Cells	--
34	chr9:73079400-73081000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
35	chr9:73080000-73080600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
36	chr9:73080000-73081000	Enhancers	iPS-15b Cell Line	embryonic stem cell
37	chr9:73080200-73080600	Enhancers	HUES6 Cell Line	embryonic stem cell
38	chr9:73080400-73080600	Enhancers	Primary T cells fromperipheralblood	blood
39	chr9:73080400-73080600	Enhancers	Esophagus	oesophagus
40	chr9:73080400-73080600	Enhancers	Spleen	Spleen
41	chr9:73080400-73081000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
42	chr9:73080400-73081200	Enhancers	Adipose Nuclei	Adipose
43	chr9:73080400-73081400	Enhancers	Psoas Muscle	Psoas
44	chr9:73080400-73081400	Enhancers	Right Atrium	heart
45	chr9:73080400-73081400	Enhancers	Right Ventricle	heart
46	chr9:73080400-73082400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
47	chr9:73080400-73082600	Enhancers	Skeletal Muscle Female	skeletal muscle
48	chr9:73080400-73083000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
49	chr9:73080400-73083600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
50	chr9:73080400-73086200	Enhancers	Left Ventricle	heart

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