Variant report

Variant	nsv893741
Chromosome Location	chr9:115862518-115891009
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:664)
CpG islands
(count:122)
Chromatin interactive
region (count:21)
LncRNA
region (count:14)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:664 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

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	CEBPZ	chr9:115890537-115890588	HepG2	liver:	n/a	n/a
8	CHD1	chr9:115874170-115874171	GM12878	blood:	n/a	n/a
9	CTCF	chr9:115875569-115875780	MCF-7	breast:	n/a	n/a
10	CTCF	chr9:115873960-115874110	AG10803	skin:	n/a	n/a
11	CTCF	chr9:115862800-115862950	HMF	breast:	n/a	chr9:115862931-115862949
12	CTCF	chr9:115875113-115875449	GM20000	blood:	n/a	chr9:115875291-115875309 chr9:115875292-115875308 chr9:115875294-115875307 chr9:115875294-115875307
13	CTCF	chr9:115873940-115874090	HEK293	kidney:	n/a	n/a
14	CTCF	chr9:115874380-115874530	BJ	skin:	n/a	n/a
15	CTCF	chr9:115873690-115874039	Pancreas_OC	pancreas:	n/a	chr9:115873826-115873839 chr9:115873826-115873839 chr9:115873825-115873841 chr9:115873824-115873842
16	CTCF	chr9:115873960-115874110	GM12878	blood:	n/a	n/a
17	CTCF	chr9:115878595-115878753	K562	blood:	n/a	n/a
18	CTCF	chr9:115873960-115874110	HCT-116	colon:	n/a	n/a
19	CTCF	chr9:115875040-115875190	HepG2	liver:	n/a	n/a
20	CTCF	chr9:115875000-115875150	GM06990	blood:	n/a	n/a
21	CTCF	chr9:115875092-115875454	LNCaP	prostate:	n/a	chr9:115875291-115875309 chr9:115875292-115875308 chr9:115875294-115875307 chr9:115875294-115875307
22	CTCF	chr9:115875062-115875405	HUVEC	blood vessel:	n/a	chr9:115875291-115875309 chr9:115875292-115875308 chr9:115875294-115875307 chr9:115875294-115875307
23	CTCF	chr9:115875726-115875813	Lung_OC	lung:	n/a	n/a
24	CTCF	chr9:115874987-115875530	A549	lung:	n/a	chr9:115875291-115875309 chr9:115875292-115875308 chr9:115875294-115875307 chr9:115875294-115875307
25	CTCF	chr9:115874166-115874247	GM19238	blood:	n/a	n/a
26	CTCF	chr9:115873940-115874090	GM12871	blood:	n/a	n/a
27	CTCF	chr9:115872463-115872615	HepG2	liver:	n/a	chr9:115872522-115872531 chr9:115872519-115872537 chr9:115872522-115872535
28	CTCF	chr9:115873960-115874110	NHDF-neo	bronchial:	n/a	n/a
29	CTCF	chr9:115875078-115875362	IMR90	lung:	n/a	chr9:115875291-115875309 chr9:115875292-115875308 chr9:115875294-115875307 chr9:115875294-115875307
30	CTCF	chr9:115875040-115875190	AG09309	skin:	n/a	n/a
31	CTCF	chr9:115873680-115874017	NHEK	skin:	n/a	chr9:115873826-115873839 chr9:115873826-115873839 chr9:115873825-115873841 chr9:115873824-115873842
32	CTCF	chr9:115873839-115874190	T-47D	breast:	n/a	n/a
33	CTCF	chr9:115873687-115874044	Kidney_OC	kidney:	n/a	chr9:115873826-115873839 chr9:115873826-115873839 chr9:115873825-115873841 chr9:115873824-115873842
34	CTCF	chr9:115875020-115875170	BJ	skin:	n/a	n/a
35	CTCF	chr9:115874790-115875350	K562	blood:	n/a	chr9:115875291-115875309 chr9:115875292-115875308 chr9:115875294-115875307 chr9:115875294-115875307
36	CTCF	chr9:115875020-115875170	GM06990	blood:	n/a	n/a
37	CTCF	chr9:115874891-115874997	HUVEC	blood vessel:	n/a	n/a
38	CTCF	chr9:115873960-115874110	NHEK	skin:	n/a	n/a
39	CTCF	chr9:115875020-115875170	HFF	foreskin:	n/a	n/a
40	CTCF	chr9:115876550-115876632	GM12878	blood:	n/a	chr9:115876598-115876611 chr9:115876596-115876614 chr9:115876602-115876611
41	CTCF	chr9:115875692-115875789	GM20000	blood:	n/a	n/a
42	CTCF	chr9:115874963-115875243	H1-hESC	embryonic stem cell:	n/a	n/a
43	CTCF	chr9:115876557-115876598	GM10248	blood:	n/a	n/a
44	CTCF	chr9:115874360-115874510	GM12865	blood:	n/a	n/a
45	CTCF	chr9:115875040-115875190	HPF	lung:	n/a	n/a
46	CTCF	chr9:115873864-115874340	MCF-7	breast:	n/a	n/a
47	CTCF	chr9:115873960-115874110	GM12867	blood:	n/a	n/a
48	CTCF	chr9:115872268-115872304	HepG2	liver:	n/a	n/a
49	CTCF	chr9:115875020-115875170	HBMEC	blood vessel:	n/a	n/a
50	CTCF	chr9:115874040-115874190	HEEpiC	esophagus:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:115874001-115874051	HPAEpiC	pulmonary alveolar:	n/a
2	chr9:115875112-115875162	AG04449	skin:	fetal
3	chr9:115875112-115875162	HAEpiC	amniotic membrane:	n/a
4	chr9:115875112-115875162	BE2_C	brain:	n/a
5	chr9:115875112-115875162	HCF	heart:	n/a
6	chr9:115875112-115875162	NHDF-neo	bronchial:	n/a
7	chr9:115875112-115875162	HUVEC	blood vessel:	n/a
8	chr9:115875112-115875162	Caco-2	colon:	n/a
9	chr9:115875112-115875162	HCM	heart:	n/a
10	chr9:115874001-115874051	PrEC	prostate:	n/a
11	chr9:115875112-115875162	CMK	blood:	n/a
12	chr9:115874001-115874051	CMK	blood:	n/a
13	chr9:115875112-115875162	SK-N-MC	brain:	n/a
14	chr9:115875112-115875162	LNCaP	prostate:	n/a
15	chr9:115874001-115874051	HCPEpiC	choroid plexus:	n/a
16	chr9:115874001-115874051	AG09319	gingival:	n/a
17	chr9:115875112-115875162	GM06990	blood:	n/a
18	chr9:115874001-115874051	NB4	blood:	n/a
19	chr9:115874001-115874051	BJ	skin:	n/a
20	chr9:115875112-115875162	SKMC	muscle:	n/a
21	chr9:115875112-115875162	HPAEpiC	pulmonary alveolar:	n/a
22	chr9:115874001-115874051	HAEpiC	amniotic membrane:	n/a
23	chr9:115874001-115874051	ECC-1	luminal epithelium:	n/a
24	chr9:115874001-115874051	PANC-1	pancreas:	n/a
25	chr9:115874001-115874051	Hepatocyte	liver:	n/a
26	chr9:115875112-115875162	SK-N-SH	brain:	n/a
27	chr9:115875112-115875162	GM12878	blood:	n/a
28	chr9:115874001-115874051	HEK293	kidney:	embryo
29	chr9:115874001-115874051	BE2_C	brain:	n/a
30	chr9:115875112-115875162	PrEC	prostate:	n/a
31	chr9:115875112-115875162	SAEC	small airway:	n/a
32	chr9:115874001-115874051	HUVEC	blood vessel:	n/a
33	chr9:115874001-115874051	HRE	kidney:	n/a
34	chr9:115875112-115875162	T-47D	breast:	n/a
35	chr9:115875112-115875162	NT2-D1	testis:	n/a
36	chr9:115874001-115874051	HEEpiC	esophagus:	n/a
37	chr9:115875112-115875162	IMR90	lung:	fetal
38	chr9:115875112-115875162	Hela-S3	cervix:	n/a
39	chr9:115875112-115875162	ovcar-3	ovarian:	n/a
40	chr9:115875112-115875162	HRE	kidney:	n/a
41	chr9:115874001-115874051	GM12891	blood:	n/a
42	chr9:115874001-115874051	HepG2	liver:	n/a
43	chr9:115874001-115874051	ProgFib	skin:	n/a
44	chr9:115875112-115875162	AG09319	gingival:	n/a
45	chr9:115875112-115875162	PFSK-1	brain:	n/a
46	chr9:115875112-115875162	K562	blood:	n/a
47	chr9:115874001-115874051	U87	brain:	n/a
48	chr9:115875112-115875162	BJ	skin:	n/a
49	chr9:115874001-115874051	IMR90	lung:	fetal
50	chr9:115874001-115874051	ovcar-3	ovarian:	n/a

(count:21 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:115890546..115893506-chr9:115895057..115896950,2	K562	blood:
2	chr9:115872624..115875532-chr9:115912017..115913734,2	MCF-7	breast:
3	chr9:115882894..115884462-chr9:115915677..115917990,2	MCF-7	breast:
4	chr9:115886125..115889063-chr9:115896987..115899858,2	K562	blood:
5	chr9:115884518..115887843-chr9:115899953..115901831,3	MCF-7	breast:
6	chr9:115857627..115859228-chr9:115862947..115865941,2	MCF-7	breast:
7	chr9:115881515..115883241-chr9:115913395..115914943,2	MCF-7	breast:
8	chr9:115875142..115875676-chr9:115912672..115913501,2	MCF-7	breast:
9	chr1:224803776..224804276-chr9:115875131..115875670,2	MCF-7	breast:
10	chr9:115890845..115895225-chr9:115895362..115900277,5	MCF-7	breast:
11	chr9:115888448..115891950-chr9:115898465..115901029,3	MCF-7	breast:
12	chr9:115887611..115890231-chr9:115913519..115916345,2	MCF-7	breast:
13	chr9:115890878..115893257-chr9:115912029..115915211,3	MCF-7	breast:
14	chr9:115884874..115886487-chr9:115927190..115929312,2	K562	blood:
15	chr9:115886679..115889181-chr9:115895702..115897217,2	MCF-7	breast:
16	chr9:115880293..115882518-chr9:115890659..115892988,2	K562	blood:
17	chr9:115888226..115890685-chr9:115891498..115893833,2	MCF-7	breast:
18	chr9:115887976..115889749-chr9:115910119..115911972,2	MCF-7	breast:
19	chr9:115882399..115884999-chr9:115891613..115894561,3	MCF-7	breast:
20	chr9:115687009..115687855-chr9:115874049..115874602,2	MCF-7	breast:
21	chr9:115880293..115882518-chr9:115890659..115892988,2	K562	blood:

(count:14 , 50 per page) page: 1

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

No data

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

Extended variants
information (count: 709 )
Associated
traits (count: 55 )

Variant overlapped rSNPs/rCNVs (count:709 , 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	rs17755206	chr9:115862518-115862519	Weak transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs192217958	chr9:115862520-115862521	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs535313618	chr9:115862526-115862527	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs555559351	chr9:115862529-115862530	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs184049916	chr9:115862550-115862551	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs111868937	chr9:115862584-115862585	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs558074175	chr9:115862589-115862590	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs577598269	chr9:115862616-115862617	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs139979905	chr9:115862620-115862621	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs369919604	chr9:115862654-115862655	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs35873238	chr9:115862676-115862677	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs544687434	chr9:115862732-115862733	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs556798385	chr9:115862830-115862831	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs1008016	chr9:115862852-115862853	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
15	rs550850117	chr9:115862854-115862855	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs188580718	chr9:115862868-115862869	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs5900037	chr9:115862893-115862894	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs528661100	chr9:115862916-115862917	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs545337118	chr9:115862918-115862919	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs565559182	chr9:115862934-115862935	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs143455625	chr9:115862943-115862944	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs146666792	chr9:115862951-115862952	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs112384267	chr9:115862958-115862959	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs567670852	chr9:115862976-115862977	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs530161022	chr9:115863018-115863019	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs554114770	chr9:115863023-115863024	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs568677643	chr9:115863059-115863060	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs571356999	chr9:115863082-115863083	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs532751259	chr9:115863130-115863131	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs565920917	chr9:115863213-115863214	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs534793308	chr9:115863226-115863227	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs181378601	chr9:115863283-115863284	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs34090890	chr9:115863291-115863292	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs571488739	chr9:115863300-115863301	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs536660354	chr9:115863335-115863336	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs556872936	chr9:115863338-115863339	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs77536664	chr9:115863365-115863366	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs547728927	chr9:115863376-115863377	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs535991294	chr9:115863505-115863506	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs116857333	chr9:115863559-115863560	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs114506529	chr9:115863660-115863661	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs184426813	chr9:115863669-115863670	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs565461011	chr9:115863675-115863676	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs575859902	chr9:115863745-115863746	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs189354306	chr9:115863746-115863747	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs566243375	chr9:115863775-115863776	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs561379668	chr9:115863800-115863801	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs530106331	chr9:115863823-115863824	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs376851810	chr9:115863841-115863842	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs547148776	chr9:115863843-115863844	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:55)

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
Bladder cancer	21909424	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:82 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:115861600-115874000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
2	chr9:115862400-115862600	ZNF genes & repeats	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr9:115862400-115862800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
4	chr9:115862600-115866000	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr9:115862800-115863600	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
6	chr9:115863600-115867000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
7	chr9:115866000-115867000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr9:115867000-115867400	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr9:115867000-115867600	Genic enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
10	chr9:115867400-115874000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr9:115867600-115874000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
12	chr9:115873800-115874000	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
13	chr9:115873800-115874000	Active TSS	Adipose Nuclei	Adipose
14	chr9:115873800-115874000	Enhancers	Osteobl	bone
15	chr9:115874000-115874200	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
16	chr9:115874000-115874200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
17	chr9:115874000-115874200	Bivalent Enhancer	Primary T helper naive cells from peripheral blood	blood
18	chr9:115874000-115874200	Bivalent Enhancer	Primary T helper naive cells fromperipheralblood	blood
19	chr9:115874000-115874200	Bivalent Enhancer	Primary T helper cells fromperipheralblood	blood
20	chr9:115874000-115874200	Bivalent Enhancer	Primary T killer memory cells from peripheral blood	blood
21	chr9:115874000-115874200	Flanking Active TSS	Adipose Nuclei	Adipose
22	chr9:115874000-115874200	Enhancers	Brain Cingulate Gyrus	brain
23	chr9:115874000-115874200	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
24	chr9:115874000-115874200	Enhancers	Brain Substantia Nigra	brain
25	chr9:115874000-115874200	Enhancers	Placenta	Placenta
26	chr9:115874000-115874400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
27	chr9:115874000-115874400	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
28	chr9:115874000-115874400	Enhancers	Primary T helper cells PMA-I stimulated	--
29	chr9:115874000-115874400	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
30	chr9:115874000-115874400	Enhancers	Brain Anterior Caudate	brain
31	chr9:115874000-115874400	Enhancers	Brain Inferior Temporal Lobe	brain
32	chr9:115874000-115874400	Bivalent Enhancer	Skeletal Muscle Female	skeletal muscle
33	chr9:115874000-115874400	Active TSS	HSMMtube	muscle
34	chr9:115874000-115874400	Active TSS	NH-A	brain
35	chr9:115874000-115874400	Flanking Active TSS	Osteobl	bone
36	chr9:115874000-115874600	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
37	chr9:115874000-115874600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
38	chr9:115874000-115874600	Flanking Active TSS	Muscle Satellite Cultured Cells	--
39	chr9:115874000-115874600	Enhancers	Spleen	Spleen
40	chr9:115874000-115875000	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
41	chr9:115874000-115875000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
42	chr9:115874000-115875000	Enhancers	Monocytes-CD14+_RO01746	blood
43	chr9:115874000-115875000	Enhancers	NHEK	skin
44	chr9:115874000-115875200	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
45	chr9:115874000-115875200	Enhancers	Primary monocytes fromperipheralblood	blood
46	chr9:115874000-115875200	Enhancers	Primary neutrophils fromperipheralblood	blood
47	chr9:115874000-115875200	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
48	chr9:115874000-115875200	Enhancers	Brain Hippocampus Middle	brain
49	chr9:115874000-115875200	Enhancers	HMEC	breast
50	chr9:115874000-115875200	Enhancers	HSMM	muscle

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