Variant report

Variant	esv2764141
Chromosome Location	chr9:16903446-17351711
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1953)
CpG islands
(count:366)
Chromatin interactive
region (count:17)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1953 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:17137735-17137782	HepG2	liver:	n/a	n/a
2	ARID3A	chr9:17116377-17116869	HepG2	liver:	n/a	n/a
3	ARID3A	chr9:17057789-17058149	HepG2	liver:	n/a	n/a
4	ARID3A	chr9:17138550-17138914	HepG2	liver:	n/a	n/a
5	ARID3A	chr9:17171685-17171982	HepG2	liver:	n/a	n/a
6	BACH1	chr9:16934659-16934853	K562	blood:	n/a	n/a
7	BACH1	chr9:16934628-16934951	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr9:17134393-17135230	H1-hESC	embryonic stem cell:	n/a	n/a
9	BATF	chr9:17057808-17058032	GM12878	blood:	n/a	n/a
10	BCL3	chr9:17134706-17135204	A549	lung:	n/a	n/a
11	BCL3	chr9:16921833-16922234	A549	lung:	n/a	chr9:16922220-16922229
12	BHLHE40	chr9:17057793-17058031	HepG2	liver:	n/a	n/a
13	BRCA1	chr9:17135427-17135902	Hela-S3	cervix:	n/a	n/a
14	BRCA1	chr9:17134617-17135090	Hela-S3	cervix:	n/a	n/a
15	BRCA1	chr9:17110915-17111000	Hela-S3	cervix:	n/a	n/a
16	BRCA1	chr9:17134759-17135091	H1-hESC	embryonic stem cell:	n/a	n/a
17	CBX3	chr9:16996867-16997187	HCT-116	colon:	n/a	n/a
18	CBX3	chr9:16996907-16997260	HCT-116	colon:	n/a	n/a
19	CEBPB	chr9:17180075-17180119	H1-hESC	embryonic stem cell:	n/a	chr9:17180087-17180098
20	CEBPB	chr9:17130354-17131057	HepG2	liver:	n/a	chr9:17130907-17130918
21	CEBPB	chr9:16996909-16997268	A549	lung:	n/a	n/a
22	CEBPB	chr9:17330165-17330444	IMR90	lung:	n/a	chr9:17330288-17330305
23	CEBPB	chr9:17021419-17021740	A549	lung:	n/a	n/a
24	CEBPB	chr9:16996936-16997307	IMR90	lung:	n/a	n/a
25	CEBPB	chr9:16923221-16923363	IMR90	lung:	n/a	n/a
26	CEBPB	chr9:16960006-16960332	IMR90	lung:	n/a	n/a
27	CEBPB	chr9:17009388-17009729	IMR90	lung:	n/a	chr9:17009575-17009584 chr9:17009575-17009584
28	CEBPB	chr9:16996962-16997280	H1-hESC	embryonic stem cell:	n/a	n/a
29	CEBPB	chr9:17346553-17346642	HepG2	liver:	n/a	n/a
30	CEBPB	chr9:17166457-17166705	A549	lung:	n/a	chr9:17166540-17166551
31	CEBPB	chr9:17033518-17033953	A549	lung:	n/a	n/a
32	CEBPB	chr9:17280466-17280824	IMR90	lung:	n/a	n/a
33	CEBPB	chr9:16996932-16997321	ECC-1	luminal epithelium:	n/a	n/a
34	CEBPB	chr9:17089875-17090011	A549	lung:	n/a	chr9:17089927-17089938
35	CEBPB	chr9:17171651-17172080	HepG2	liver:	n/a	n/a
36	CEBPB	chr9:16996969-16997259	HepG2	liver:	n/a	n/a
37	CEBPB	chr9:17021301-17021774	Hela-S3	cervix:	n/a	n/a
38	CEBPB	chr9:17104175-17104375	A549	lung:	n/a	n/a
39	CEBPB	chr9:17130336-17130640	H1-hESC	embryonic stem cell:	n/a	n/a
40	CEBPB	chr9:17021416-17021683	HepG2	liver:	n/a	n/a
41	CEBPB	chr9:16996916-16997232	MCF-7	breast:	n/a	n/a
42	CEBPB	chr9:16982707-16982907	A549	lung:	n/a	n/a
43	CEBPB	chr9:16927604-16927635	HepG2	liver:	n/a	n/a
44	CEBPB	chr9:16996967-16997310	A549	lung:	n/a	n/a
45	CEBPB	chr9:17057772-17058066	HepG2	liver:	n/a	n/a
46	CEBPB	chr9:16964093-16964576	IMR90	lung:	n/a	chr9:16964182-16964194
47	CEBPB	chr9:16985908-16986453	IMR90	lung:	n/a	n/a
48	CEBPB	chr9:17167623-17167870	HepG2	liver:	n/a	chr9:17167704-17167715
49	CEBPB	chr9:17021238-17021833	IMR90	lung:	n/a	n/a
50	CEBPB	chr9:17009423-17009667	A549	lung:	n/a	chr9:17009575-17009584 chr9:17009575-17009584

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:17137020-17137070	HNPCEpiC	eye:	n/a
2	chr9:17132989-17133039	U87	brain:	n/a
3	chr9:17134569-17134619	NHBE	bronchial:	n/a
4	chr9:17135705-17135755	AoSMC	blood vessel:	n/a
5	chr9:17135705-17135755	ECC-1	luminal epithelium:	n/a
6	chr9:17134842-17134892	SK-N-SH	brain:	n/a
7	chr9:17135705-17135755	CMK	blood:	n/a
8	chr9:17137020-17137070	U87	brain:	n/a
9	chr9:17137020-17137070	BE2_C	brain:	n/a
10	chr9:17132989-17133039	MCF-7	breast:	n/a
11	chr9:17134842-17134892	GM06990	blood:	n/a
12	chr9:17134842-17134892	AG09319	gingival:	n/a
13	chr9:17137020-17137070	H1-hESC	embryonic stem cell:	embryo
14	chr9:17134569-17134619	SKMC	muscle:	n/a
15	chr9:17134569-17134619	GM12891	blood:	n/a
16	chr9:16964111-16964161	HIPEpiC	eye:	n/a
17	chr9:17137020-17137070	NB4	blood:	n/a
18	chr9:17137020-17137070	HEK293	kidney:	embryo
19	chr9:16964111-16964161	HMEC	breast:	n/a
20	chr9:17132989-17133039	PANC-1	pancreas:	n/a
21	chr9:17134842-17134892	MCF10A-Er-Src	breast:	n/a
22	chr9:17137020-17137070	PrEC	prostate:	n/a
23	chr9:17135705-17135755	AG09319	gingival:	n/a
24	chr9:17134569-17134619	K562	blood:	n/a
25	chr9:17134842-17134892	NB4	blood:	n/a
26	chr9:17134569-17134619	A549	lung:	n/a
27	chr9:16964111-16964161	HCT-116	colon:	n/a
28	chr9:17132989-17133039	HRCEpiC	kidney:	n/a
29	chr9:16964111-16964161	HRCEpiC	kidney:	n/a
30	chr9:17134569-17134619	SK-N-SH_RA	brain:	n/a
31	chr9:17137020-17137070	PANC-1	pancreas:	n/a
32	chr9:17132989-17133039	NHBE	bronchial:	n/a
33	chr9:16964111-16964161	BJ	skin:	n/a
34	chr9:17134569-17134619	HEEpiC	esophagus:	n/a
35	chr9:17134569-17134619	HAEpiC	amniotic membrane:	n/a
36	chr9:16964111-16964161	Jurkat	blood:	n/a
37	chr9:17135705-17135755	HCT-116	colon:	n/a
38	chr9:17135705-17135755	SK-N-SH	brain:	n/a
39	chr9:17137020-17137070	GM19239	blood:	n/a
40	chr9:17134569-17134619	NH-A	brain:	n/a
41	chr9:17134842-17134892	NHBE	bronchial:	n/a
42	chr9:17134569-17134619	PFSK-1	brain:	n/a
43	chr9:16964111-16964161	U87	brain:	n/a
44	chr9:16964111-16964161	NB4	blood:	n/a
45	chr9:16964111-16964161	GM12892	blood:	n/a
46	chr9:17134842-17134892	U87	brain:	n/a
47	chr9:17134569-17134619	ProgFib	skin:	n/a
48	chr9:17134569-17134619	HCPEpiC	choroid plexus:	n/a
49	chr9:17137020-17137070	SKMC	muscle:	n/a
50	chr9:17132989-17133039	ProgFib	skin:	n/a

(count:17 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:17317781..17319396-chr9:17320003..17322475,2	MCF-7	breast:
2	chr9:17004932..17007249-chr9:17011274..17013104,2	MCF-7	breast:
3	chr5:43121428..43122109-chr9:17134722..17135406,2	Hela-S3	cervix:
4	chr9:17004932..17007249-chr9:17011274..17013104,2	MCF-7	breast:
5	chr9:17317781..17319396-chr9:17320003..17322475,2	MCF-7	breast:
6	chr15:23810837..23811461-chr9:17134816..17135417,2	NB4	blood:
7	chr1:11969364..11970234-chr9:17134620..17135236,2	Hela-S3	cervix:
8	chr9:17063303..17064146-chr9:17462547..17463504,3	MCF-7	breast:
9	chr9:17219375..17219930-chr9:17402045..17403347,3	MCF-7	breast:
10	chr9:17116233..17116835-chr9:17462927..17463473,2	MCF-7	breast:
11	chr9:17116046..17116795-chr9:17462771..17463533,2	MCF-7	breast:
12	chr17:59651978..59652576-chr9:17247861..17248361,2	MCF-7	breast:
13	chr13:49549584..49550165-chr9:17134587..17135235,2	NB4	blood:
14	chr9:17219048..17219921-chr9:17462587..17463121,2	MCF-7	breast:
15	chr9:17219155..17220052-chr9:17401883..17402825,5	MCF-7	breast:
16	chr9:17116081..17117141-chr9:17402172..17402905,3	MCF-7	breast:
17	chr6:692813..693544-chr9:17134998..17135501,2	NB4	blood:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-BNC2-3	chr9:17322212-17322433	uc_253_-
2	lnc-CNTLN-1	chr9:17112271-17112813	ENSG00000237153.1
3	lnc-BNC2-2	chr9:17108302-17108602	NONHSAT130300
4	lnc-SH3GL2-3	chr9:17322212-17322433	uc_253_+
5	lnc-CNTLN-4	chr9:17053899-17054200	NONHSAT130298
6	lnc-CNTLN-1	chr9:17048917-17049039	ENSG00000237153.1

No data

Variant related genes	Relation type
ENSG00000226470	TF binding region
ENSG00000237083	TF binding region
RN7SL720P	TF binding region
ENSG00000237153	TF binding region
CNTLN	TF binding region
ENSG00000226470	CpG island
ENSG00000237083	CpG island
RN7SL720P	CpG island
ENSG00000237153	CpG island
CNTLN	CpG island
ENSG00000179455	chromatin interactions
ENSG00000102531	chromatin interactions
ENSG00000112685	chromatin interactions
ENSG00000172262	chromatin interactions
ENSG00000201801	chromatin interactions

Extended variants
information (count: 17489 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:17489 , 50 per page) page: 1 2 3 4 5 6 7 ... 350

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10733333	chr9:16903446-16903447	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs550962880	chr9:16903460-16903461	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs10733334	chr9:16903490-16903491	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs189823891	chr9:16903521-16903522	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs369485513	chr9:16903562-16903563	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs192782044	chr9:16903572-16903573	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs11790433	chr9:16903574-16903575	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs574754984	chr9:16903593-16903594	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs548292917	chr9:16903597-16903598	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs55761409	chr9:16903603-16903604	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs185210892	chr9:16903611-16903612	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs557033856	chr9:16903634-16903635	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs10756834	chr9:16903652-16903653	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs569190747	chr9:16903661-16903662	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs539211549	chr9:16903664-16903665	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs370137722	chr9:16903668-16903669	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs58134658	chr9:16903722-16903723	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs566433850	chr9:16903732-16903733	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs78488263	chr9:16903740-16903741	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs564554997	chr9:16903766-16903767	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs189170855	chr9:16903771-16903772	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs573272345	chr9:16903788-16903789	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs537460584	chr9:16903790-16903791	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs573456896	chr9:16903837-16903838	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs10810661	chr9:16903850-16903851	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs578201244	chr9:16903860-16903861	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs545270314	chr9:16903900-16903901	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs560781364	chr9:16903907-16903908	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs181832509	chr9:16903908-16903909	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs7029285	chr9:16903948-16903949	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs561389319	chr9:16903958-16903959	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs531703344	chr9:16903982-16903983	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs369465573	chr9:16903988-16903989	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs7032158	chr9:16904047-16904048	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs386733159	chr9:16904080-16904081	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs186486418	chr9:16904102-16904103	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs7032644	chr9:16904141-16904142	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs115515145	chr9:16904184-16904185	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs548630559	chr9:16904190-16904191	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs150999884	chr9:16904193-16904194	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs374225029	chr9:16904196-16904197	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs7032420	chr9:16904202-16904203	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs188121210	chr9:16904203-16904204	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs77037377	chr9:16904244-16904245	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs554052160	chr9:16904248-16904249	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs115418627	chr9:16904275-16904276	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs543259402	chr9:16904279-16904280	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs7032909	chr9:16904303-16904304	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs180889050	chr9:16904324-16904325	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs543829124	chr9:16904331-16904332	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:90)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
abnormal development	18461090	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Breast cancer	16608533	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	16272173	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	17133270	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Cervical cancer	21063398	CNVD
Retinoblastoma	22278416	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Melanoma	18172304	CNVD
Biliary cancer	19435499	CNVD
Gastric cancer	21586687	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myopathy	18421352	CNVD
Neuroblastoma	18664255	CNVD
Acute lymphoblastic leukemia	18957548	CNVD
Myeloproliferative neoplasm	17564968	CNVD
Malignant meningioma	17937814	CNVD
Glioma	21971842	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	17603634	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oligodendroglial tumors	17285580	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chordoma	21602918	CNVD
Renal cell carcinoma	18592004	CNVD
Developmental delay	19490664	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
microdeletion syndrome	16199537	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Cancer	20164919	CNVD
Chronic myeloid leukemia	21384125	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Lung cancer	18438408	CNVD
Urothelial carcinoma	21177765	CNVD
Oral cancer	21386901	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	21785460	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21858162	CNVD
Renal cell carcinoma	21668985	CNVD
Myelodysplastic syndrome	21251322	CNVD
Autism	22495311	CNVD
Hepatocellular carcinoma	18803288	CNVD
Metanephric adenoma	20802469	CNVD
Developmental delay	21147756	CNVD
Pilocytic astrocytoma	18670637	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Melanoma	22183965	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Myelofibrosis	22110671	CNVD
Glycine encephalopathy	21572526	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Non-small cell lung cancer	19010865	CNVD
Myoepithelioma	18604193	CNVD
Glioblastoma multiforme	18628472	CNVD
Breast cancer	21611746	CNVD
Breast cancer	21364760	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Medulloblastoma	21163964	CNVD

Chromatin state (count:2190 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:16902000-16914800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
2	chr9:16908200-16908600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
3	chr9:16911800-16912800	Enhancers	Muscle Satellite Cultured Cells	--
4	chr9:16911800-16912800	Enhancers	A549	lung
5	chr9:16912200-16912800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
6	chr9:16912200-16912800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
7	chr9:16912200-16912800	Enhancers	Osteobl	bone
8	chr9:16912800-16914800	Weak transcription	Osteobl	bone
9	chr9:16912800-16915200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
10	chr9:16912800-16921800	Weak transcription	Muscle Satellite Cultured Cells	--
11	chr9:16912800-16928000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
12	chr9:16914800-16915000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr9:16914800-16915600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr9:16914800-16915600	Enhancers	Adipose Nuclei	Adipose
15	chr9:16914800-16915800	Enhancers	Osteobl	bone
16	chr9:16915000-16915200	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
17	chr9:16915000-16915600	Enhancers	NHDF-Ad	bronchial
18	chr9:16915200-16915400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
19	chr9:16915200-16915600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
20	chr9:16915200-16915800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
21	chr9:16915400-16915800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
22	chr9:16915400-16915800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
23	chr9:16915400-16915800	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
24	chr9:16915400-16915800	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
25	chr9:16915400-16915800	Enhancers	Psoas Muscle	Psoas
26	chr9:16915400-16915800	Enhancers	HSMM	muscle
27	chr9:16915800-16918800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
28	chr9:16915800-16921600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr9:16915800-16923600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
30	chr9:16915800-16928200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
31	chr9:16916400-16916600	Enhancers	Right Atrium	heart
32	chr9:16918600-16919600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
33	chr9:16918800-16919000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
34	chr9:16919000-16919400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
35	chr9:16919400-16919800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
36	chr9:16919600-16920000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
37	chr9:16921600-16922000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
38	chr9:16921600-16922200	Enhancers	NHDF-Ad	bronchial
39	chr9:16921600-16922800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
40	chr9:16921600-16923800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
41	chr9:16921800-16922000	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
42	chr9:16921800-16922000	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
43	chr9:16921800-16922200	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
44	chr9:16921800-16922200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
45	chr9:16921800-16922200	Enhancers	A549	lung
46	chr9:16921800-16922200	Enhancers	NHEK	skin
47	chr9:16921800-16922200	Enhancers	Osteobl	bone
48	chr9:16921800-16922400	Enhancers	Muscle Satellite Cultured Cells	--
49	chr9:16922200-16924400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
50	chr9:16922400-16923400	Weak transcription	Muscle Satellite Cultured Cells	--

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