Variant report

Variant	nsv1040513
Chromosome Location	chr9:115854339-115885060
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	BATF	chr9:115873657-115873969	GM12878	blood:	n/a	n/a
2	BATF	chr9:115875188-115875441	GM12878	blood:	n/a	n/a
3	CBX3	chr9:115873150-115874076	K562	blood:	n/a	n/a
4	CBX3	chr9:115875083-115875868	K562	blood:	n/a	n/a
5	CCNT2	chr9:115862949-115863058	K562	blood:	n/a	n/a
6	CEBPB	chr9:115875081-115875193	H1-hESC	embryonic stem cell:	n/a	n/a
7	CHD1	chr9:115874170-115874171	GM12878	blood:	n/a	n/a
8	CTCF	chr9:115876505-115876679	MCF-7	breast:	n/a	chr9:115876598-115876611 chr9:115876596-115876614 chr9:115876602-115876611
9	CTCF	chr9:115874946-115875570	A549	lung:	n/a	chr9:115875291-115875309 chr9:115875292-115875308 chr9:115875294-115875307 chr9:115875294-115875307
10	CTCF	chr9:115873354-115874079	K562	blood:	n/a	chr9:115873826-115873839 chr9:115873826-115873839 chr9:115873825-115873841 chr9:115873824-115873842
11	CTCF	chr9:115872226-115872332	MCF-7	breast:	n/a	n/a
12	CTCF	chr9:115868126-115868225	GM13976	blood:	n/a	n/a
13	CTCF	chr9:115873451-115873524	K562	blood:	n/a	n/a
14	CTCF	chr9:115875020-115875170	HEK293	kidney:	n/a	n/a
15	CTCF	chr9:115875040-115875190	HCM	heart:	n/a	n/a
16	CTCF	chr9:115873960-115874110	SK-N-SH_RA	brain:	n/a	n/a
17	CTCF	chr9:115869554-115869613	GM13976	blood:	n/a	n/a
18	CTCF	chr9:115875078-115875362	IMR90	lung:	n/a	chr9:115875291-115875309 chr9:115875292-115875308 chr9:115875294-115875307 chr9:115875294-115875307
19	CTCF	chr9:115873700-115874001	A549	lung:	n/a	chr9:115873826-115873839 chr9:115873826-115873839 chr9:115873825-115873841 chr9:115873824-115873842
20	CTCF	chr9:115875020-115875170	GM12870	blood:	n/a	n/a
21	CTCF	chr9:115875075-115875467	Spleen_OC	spleen:	n/a	chr9:115875291-115875309 chr9:115875292-115875308 chr9:115875294-115875307 chr9:115875294-115875307
22	CTCF	chr9:115873960-115874110	AG09319	gingival:	n/a	n/a
23	CTCF	chr9:115875000-115875150	GM12873	blood:	n/a	n/a
24	CTCF	chr9:115875040-115875190	HPAF	blood vessel:	n/a	n/a
25	CTCF	chr9:115875692-115875789	GM20000	blood:	n/a	n/a
26	CTCF	chr9:115873689-115874004	Hela-S3	cervix:	n/a	chr9:115873826-115873839 chr9:115873826-115873839 chr9:115873825-115873841 chr9:115873824-115873842
27	CTCF	chr9:115873865-115874104	T-47D	breast:	n/a	n/a
28	CTCF	chr9:115873706-115874057	HUVEC	blood vessel:	n/a	chr9:115873826-115873839 chr9:115873826-115873839 chr9:115873825-115873841 chr9:115873824-115873842
29	CTCF	chr9:115873763-115874162	GM12878	blood:	n/a	chr9:115873826-115873839 chr9:115873826-115873839 chr9:115873825-115873841 chr9:115873824-115873842
30	CTCF	chr9:115875020-115875170	HA-sp	spinal cord:	n/a	n/a
31	CTCF	chr9:115875020-115875170	Hela-S3	cervix:	n/a	n/a
32	CTCF	chr9:115873662-115874011	MCF-7	breast:	n/a	chr9:115873826-115873839 chr9:115873826-115873839 chr9:115873825-115873841 chr9:115873824-115873842
33	CTCF	chr9:115874460-115874610	GM12878	blood:	n/a	n/a
34	CTCF	chr9:115873940-115874090	GM12874	blood:	n/a	n/a
35	CTCF	chr9:115875020-115875170	AG04449	skin:	n/a	n/a
36	CTCF	chr9:115873853-115874091	H1-hESC	embryonic stem cell:	n/a	n/a
37	CTCF	chr9:115875040-115875190	HCPEpiC	choroid plexus:	n/a	n/a
38	CTCF	chr9:115873540-115874027	GM19238	blood:	n/a	chr9:115873826-115873839 chr9:115873826-115873839 chr9:115873825-115873841 chr9:115873824-115873842
39	CTCF	chr9:115875020-115875170	GM12865	blood:	n/a	n/a
40	CTCF	chr9:115875569-115875780	MCF-7	breast:	n/a	n/a
41	CTCF	chr9:115872470-115872595	MCF-7	breast:	n/a	chr9:115872522-115872531 chr9:115872519-115872537 chr9:115872522-115872535
42	CTCF	chr9:115873695-115874047	GM13977	blood:	n/a	chr9:115873826-115873839 chr9:115873826-115873839 chr9:115873825-115873841 chr9:115873824-115873842
43	CTCF	chr9:115878641-115878718	Hela-S3	cervix:	n/a	n/a
44	CTCF	chr9:115872415-115872611	MCF-7	breast:	n/a	chr9:115872522-115872531 chr9:115872519-115872537 chr9:115872522-115872535
45	CTCF	chr9:115875020-115875170	GM12868	blood:	n/a	n/a
46	CTCF	chr9:115873472-115874029	GM19240	blood:	n/a	chr9:115873826-115873839 chr9:115873826-115873839 chr9:115873825-115873841 chr9:115873824-115873842
47	CTCF	chr9:115875020-115875170	AG10803	skin:	n/a	n/a
48	CTCF	chr9:115875040-115875190	BJ	skin:	n/a	n/a
49	CTCF	chr9:115873960-115874110	BE2_C	brain:	n/a	n/a
50	CTCF	chr9:115873419-115873429	GM19240	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:115874001-115874051	GM19239	blood:	n/a
2	chr9:115874001-115874051	BE2_C	brain:	n/a
3	chr9:115875112-115875162	HCF	heart:	n/a
4	chr9:115874001-115874051	AG09319	gingival:	n/a
5	chr9:115874001-115874051	NHBE	bronchial:	n/a
6	chr9:115875112-115875162	BJ	skin:	n/a
7	chr9:115875112-115875162	SKMC	muscle:	n/a
8	chr9:115875112-115875162	H1-hESC	embryonic stem cell:	embryo
9	chr9:115875112-115875162	HEK293	kidney:	embryo
10	chr9:115874001-115874051	IMR90	lung:	fetal
11	chr9:115875112-115875162	ProgFib	skin:	n/a
12	chr9:115874001-115874051	HUVEC	blood vessel:	n/a
13	chr9:115875112-115875162	ovcar-3	ovarian:	n/a
14	chr9:115875112-115875162	AG09319	gingival:	n/a
15	chr9:115874001-115874051	GM12892	blood:	n/a
16	chr9:115875112-115875162	HNPCEpiC	eye:	n/a
17	chr9:115875112-115875162	SK-N-SH_RA	brain:	n/a
18	chr9:115874001-115874051	Jurkat	blood:	n/a
19	chr9:115875112-115875162	HIPEpiC	eye:	n/a
20	chr9:115875112-115875162	GM12878	blood:	n/a
21	chr9:115875112-115875162	ECC-1	luminal epithelium:	n/a
22	chr9:115874001-115874051	RPTEC	kidney:	n/a
23	chr9:115874001-115874051	AG04450	lung:	fetal
24	chr9:115874001-115874051	ProgFib	skin:	n/a
25	chr9:115875112-115875162	BE2_C	brain:	n/a
26	chr9:115874001-115874051	PANC-1	pancreas:	n/a
27	chr9:115875112-115875162	Caco-2	colon:	n/a
28	chr9:115874001-115874051	K562	blood:	n/a
29	chr9:115874001-115874051	HepG2	liver:	n/a
30	chr9:115874001-115874051	H1-hESC	embryonic stem cell:	embryo
31	chr9:115875112-115875162	NT2-D1	testis:	n/a
32	chr9:115874001-115874051	SK-N-SH	brain:	n/a
33	chr9:115874001-115874051	HNPCEpiC	eye:	n/a
34	chr9:115874001-115874051	MCF-7	breast:	n/a
35	chr9:115874001-115874051	HAEpiC	amniotic membrane:	n/a
36	chr9:115875112-115875162	LNCaP	prostate:	n/a
37	chr9:115875112-115875162	NHDF-neo	bronchial:	n/a
38	chr9:115874001-115874051	ovcar-3	ovarian:	n/a
39	chr9:115875112-115875162	HRCEpiC	kidney:	n/a
40	chr9:115875112-115875162	HCPEpiC	choroid plexus:	n/a
41	chr9:115875112-115875162	MCF-7	breast:	n/a
42	chr9:115875112-115875162	T-47D	breast:	n/a
43	chr9:115874001-115874051	SAEC	small airway:	n/a
44	chr9:115875112-115875162	GM06990	blood:	n/a
45	chr9:115875112-115875162	CMK	blood:	n/a
46	chr9:115875112-115875162	HL-60	blood:	n/a
47	chr9:115874001-115874051	Hela-S3	cervix:	n/a
48	chr9:115875112-115875162	GM12892	blood:	n/a
49	chr9:115875112-115875162	AG10803	skin:	n/a
50	chr9:115875112-115875162	SK-N-MC	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr9:115857627..115859228-chr9:115862947..115865941,2	MCF-7	breast:
2	chr9:115857627..115859228-chr9:115862947..115865941,2	MCF-7	breast:
3	chr9:115872624..115875532-chr9:115912017..115913734,2	MCF-7	breast:
4	chr9:115856198..115858417-chr9:115859044..115860820,2	MCF-7	breast:
5	chr9:115884518..115887843-chr9:115899953..115901831,3	MCF-7	breast:
6	chr9:115875142..115875676-chr9:115912672..115913501,2	MCF-7	breast:
7	chr9:115882894..115884462-chr9:115915677..115917990,2	MCF-7	breast:
8	chr9:115884874..115886487-chr9:115927190..115929312,2	K562	blood:
9	chr9:115853301..115854826-chr9:115855514..115857498,2	K562	blood:
10	chr9:115853301..115854826-chr9:115855514..115857498,2	K562	blood:
11	chr1:224803776..224804276-chr9:115875131..115875670,2	MCF-7	breast:
12	chr9:115880293..115882518-chr9:115890659..115892988,2	K562	blood:
13	chr9:115687009..115687855-chr9:115874049..115874602,2	MCF-7	breast:
14	chr9:115856198..115858417-chr9:115859044..115860820,2	MCF-7	breast:
15	chr9:115882399..115884999-chr9:115891613..115894561,3	MCF-7	breast:
16	chr9:115881515..115883241-chr9:115913395..115914943,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SLC31A2-1	chr9:115875176-115875443	NONHSAT134170
2	lnc-ZFP37-2	chr9:115867003-115872433	ENSG00000225684
3	lnc-ZFP37-2	chr9:115873690-115873780	ENSG00000225684
4	lnc-ZFP37-2	chr9:115873190-115873296	ENSG00000225684
5	lnc-SLC31A2-1	chr9:115876700-115882126	NONHSAT134170
6	lnc-SLC31A2-1	chr9:115875353-115875443	ENSG00000231528
7	lnc-ZFP37-2	chr9:115873190-115873753	ENSG00000225684
8	lnc-ZFP37-2	chr9:115873190-115873296	NONHSAT134034
9	lnc-SLC31A2-1	chr9:115876700-115882126	ENSG00000231528
10	lnc-ZFP37-2	chr9:115865618-115872433	ENSG00000225684
11	lnc-ZFP37-2	chr9:115867003-115872433	NONHSAT134034
12	lnc-SLC31A2-1	chr9:115875837-115875943	ENSG00000231528
13	lnc-ZFP37-2	chr9:115873690-115873957	NONHSAT134034
14	lnc-SLC31A2-1	chr9:115875837-115875943	NONHSAT134170

Variant related genes	Relation type
FAM225B	TF binding region
FAM225A	TF binding region
FAM225B	CpG island
FAM225A	CpG island
ENSG00000143786	chromatin interactions
ENSG00000136867	chromatin interactions
ENSG00000233384	chromatin interactions

Extended variants
information (count: 750 )
Associated
traits (count: 56 )

Variant overlapped rSNPs/rCNVs (count:750 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs543422440	chr9:115854416-115854417	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
2	rs60064995	chr9:115854451-115854452	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs116104383	chr9:115854452-115854453	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs189852743	chr9:115854471-115854472	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs538179403	chr9:115854482-115854483	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs183246921	chr9:115854508-115854509	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs186484517	chr9:115854510-115854511	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs16933526	chr9:115854519-115854520	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs571590915	chr9:115854595-115854596	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs537075052	chr9:115854616-115854617	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs368617628	chr9:115854640-115854641	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs60631544	chr9:115854654-115854655	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs12001237	chr9:115854670-115854671	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
14	rs191458089	chr9:115854685-115854686	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs141620140	chr9:115854689-115854690	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs553429375	chr9:115854759-115854760	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs572188909	chr9:115854781-115854782	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs145118088	chr9:115854833-115854834	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs148343902	chr9:115854836-115854837	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs141578839	chr9:115854883-115854884	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs150894326	chr9:115854900-115854901	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs537248279	chr9:115854912-115854913	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs183569131	chr9:115854928-115854929	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs550446615	chr9:115854996-115854997	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs200416725	chr9:115854997-115854998	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs201305777	chr9:115854998-115854999	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs188507871	chr9:115855053-115855054	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs375805821	chr9:115855073-115855074	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs386737757	chr9:115855084-115855085	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs540431595	chr9:115855086-115855087	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs543840217	chr9:115855087-115855088	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs528692882	chr9:115855112-115855113	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs192890500	chr9:115855118-115855119	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs111861342	chr9:115855186-115855187	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs182544337	chr9:115855227-115855228	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs534902477	chr9:115855253-115855254	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs186509634	chr9:115855259-115855260	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs77904381	chr9:115855320-115855321	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs536641709	chr9:115855341-115855342	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs546814214	chr9:115855349-115855350	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs74480008	chr9:115855356-115855357	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs534836589	chr9:115855409-115855410	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs577560153	chr9:115855426-115855427	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs367855870	chr9:115855474-115855475	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs557952986	chr9:115855489-115855490	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs191355188	chr9:115855558-115855559	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs537298892	chr9:115855581-115855582	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs531467243	chr9:115855598-115855599	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs557215370	chr9:115855627-115855628	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs573593728	chr9:115855632-115855633	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:56)

Disease	PMID	Source
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
T-cell prolymphocytic leukemia	19278963	CNVD
Urothelial carcinoma	21177765	CNVD
Renal cell carcinoma	21668985	CNVD
Autism	22495311	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	16751803	CNVD
Myelofibrosis	22110671	CNVD
lymphocytic leukemia	21291569	CNVD
Leukemia	17361228	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Glioblastoma	16823260	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
Lung cancer	18438408	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	17603634	CNVD
Acute myeloid leukemia	20729466	CNVD
Oral cancer	21386901	CNVD
Prostate cancer	18632612	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Gastric cancer	17908304	CNVD
small cell lung cancer	20016488	CNVD
Cardiac fibroma	18329553	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Testicular germ cell tumor	18059402	CNVD
Breast cancer	21364760	CNVD
Developmental delay	21147756	CNVD
Lung cancer	19147751	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Melanoma	18172304	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	22522925	CNVD
Melanoma	20877625	CNVD
Bladder cancer	21909424	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:90 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:115854400-115854800	ZNF genes & repeats	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
2	chr9:115854800-115855200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
3	chr9:115855200-115855600	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
4	chr9:115855600-115857200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
5	chr9:115857000-115857600	ZNF genes & repeats	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr9:115857200-115858400	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
7	chr9:115858400-115859000	ZNF genes & repeats	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr9:115858800-115859000	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr9:115858800-115859000	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
10	chr9:115858800-115859000	Enhancers	Gastric	stomach
11	chr9:115859000-115861800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
12	chr9:115859000-115862400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr9:115861600-115874000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr9:115861800-115862400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
15	chr9:115862400-115862600	ZNF genes & repeats	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr9:115862400-115862800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
17	chr9:115862600-115866000	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
18	chr9:115862800-115863600	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
19	chr9:115863600-115867000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
20	chr9:115866000-115867000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
21	chr9:115867000-115867400	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr9:115867000-115867600	Genic enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
23	chr9:115867400-115874000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
24	chr9:115867600-115874000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
25	chr9:115873800-115874000	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
26	chr9:115873800-115874000	Active TSS	Adipose Nuclei	Adipose
27	chr9:115873800-115874000	Enhancers	Osteobl	bone
28	chr9:115874000-115874200	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
29	chr9:115874000-115874200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
30	chr9:115874000-115874200	Bivalent Enhancer	Primary T helper naive cells from peripheral blood	blood
31	chr9:115874000-115874200	Bivalent Enhancer	Primary T helper naive cells fromperipheralblood	blood
32	chr9:115874000-115874200	Bivalent Enhancer	Primary T helper cells fromperipheralblood	blood
33	chr9:115874000-115874200	Bivalent Enhancer	Primary T killer memory cells from peripheral blood	blood
34	chr9:115874000-115874200	Flanking Active TSS	Adipose Nuclei	Adipose
35	chr9:115874000-115874200	Enhancers	Brain Cingulate Gyrus	brain
36	chr9:115874000-115874200	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
37	chr9:115874000-115874200	Enhancers	Brain Substantia Nigra	brain
38	chr9:115874000-115874200	Enhancers	Placenta	Placenta
39	chr9:115874000-115874400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
40	chr9:115874000-115874400	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
41	chr9:115874000-115874400	Enhancers	Primary T helper cells PMA-I stimulated	--
42	chr9:115874000-115874400	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
43	chr9:115874000-115874400	Enhancers	Brain Anterior Caudate	brain
44	chr9:115874000-115874400	Enhancers	Brain Inferior Temporal Lobe	brain
45	chr9:115874000-115874400	Bivalent Enhancer	Skeletal Muscle Female	skeletal muscle
46	chr9:115874000-115874400	Active TSS	HSMMtube	muscle
47	chr9:115874000-115874400	Active TSS	NH-A	brain
48	chr9:115874000-115874400	Flanking Active TSS	Osteobl	bone
49	chr9:115874000-115874600	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
50	chr9:115874000-115874600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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