Variant report

Variant	esv2759680
Chromosome Location	chr9:21499624-21526526
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	BCL3	chr9:21501331-21508410	A549	lung:	n/a	chr9:21506204-21506213
2	BCL3	chr9:21519608-21520690	A549	lung:	n/a	chr9:21519928-21519937
3	BCL3	chr9:21499752-21501285	A549	lung:	n/a	n/a
4	BCL3	chr9:21499921-21500395	A549	lung:	n/a	n/a
5	BCL3	chr9:21506616-21507704	A549	lung:	n/a	n/a
6	BCL3	chr9:21501977-21502583	A549	lung:	n/a	n/a
7	BCL3	chr9:21508689-21509632	A549	lung:	n/a	n/a
8	BCL3	chr9:21503475-21506429	A549	lung:	n/a	chr9:21506204-21506213
9	BCL3	chr9:21500520-21501100	A549	lung:	n/a	n/a
10	CBX3	chr9:21519763-21526025	HCT-116	colon:	n/a	n/a
11	CBX3	chr9:21520811-21522028	HCT-116	colon:	n/a	n/a
12	CBX3	chr9:21526174-21527163	HCT-116	colon:	n/a	n/a
13	CBX3	chr9:21522147-21524471	HCT-116	colon:	n/a	n/a
14	CEBPB	chr9:21519556-21521968	HCT-116	colon:	n/a	n/a
15	CEBPB	chr9:21506801-21507249	Hela-S3	cervix:	n/a	n/a
16	CEBPB	chr9:21513524-21513835	IMR90	lung:	n/a	n/a
17	CEBPB	chr9:21501197-21501480	A549	lung:	n/a	n/a
18	CEBPB	chr9:21519283-21525730	HCT-116	colon:	n/a	n/a
19	CEBPB	chr9:21506792-21507249	IMR90	lung:	n/a	n/a
20	CEBPB	chr9:21506492-21507694	HCT-116	colon:	n/a	chr9:21507245-21507257
21	CTCF	chr9:21502460-21502610	NHDF-neo	bronchial:	n/a	n/a
22	CTCF	chr9:21500904-21500959	GM20000	blood:	n/a	n/a
23	CTCF	chr9:21509715-21509808	GM10248	blood:	n/a	n/a
24	CTCF	chr9:21512071-21512100	Fibrobl	skin:	n/a	n/a
25	EGR1	chr9:21523516-21524894	HCT-116	colon:	n/a	n/a
26	ELF1	chr9:21506772-21507158	A549	lung:	n/a	chr9:21507058-21507069
27	ELF1	chr9:21508706-21509493	HCT-116	colon:	n/a	n/a
28	ELF1	chr9:21519892-21526918	HCT-116	colon:	n/a	n/a
29	EP300	chr9:21506819-21507193	Hela-S3	cervix:	n/a	n/a
30	FOS	chr9:21508367-21508583	MCF10A-Er-Src	breast:	n/a	chr9:21508424-21508431 chr9:21508421-21508432 chr9:21508423-21508431 chr9:21508423-21508432
31	FOS	chr9:21513418-21513843	MCF10A-Er-Src	breast:	n/a	n/a
32	FOS	chr9:21505465-21505789	MCF10A-Er-Src	breast:	n/a	n/a
33	FOS	chr9:21513445-21513869	MCF10A-Er-Src	breast:	n/a	n/a
34	FOS	chr9:21505386-21505787	MCF10A-Er-Src	breast:	n/a	n/a
35	FOS	chr9:21506828-21507267	MCF10A-Er-Src	breast:	n/a	n/a
36	FOS	chr9:21506889-21507250	MCF10A-Er-Src	breast:	n/a	n/a
37	FOS	chr9:21506846-21507207	MCF10A-Er-Src	breast:	n/a	n/a
38	FOS	chr9:21519654-21519864	MCF10A-Er-Src	breast:	n/a	n/a
39	FOS	chr9:21506911-21507422	HUVEC	blood vessel:	n/a	n/a
40	FOS	chr9:21505429-21505786	MCF10A-Er-Src	breast:	n/a	n/a
41	FOS	chr9:21519640-21519884	MCF10A-Er-Src	breast:	n/a	n/a
42	FOS	chr9:21506738-21507319	MCF10A-Er-Src	breast:	n/a	n/a
43	FOS	chr9:21519635-21519835	MCF10A-Er-Src	breast:	n/a	n/a
44	FOS	chr9:21513438-21513821	MCF10A-Er-Src	breast:	n/a	n/a
45	FOS	chr9:21508277-21508670	HUVEC	blood vessel:	n/a	chr9:21508424-21508431 chr9:21508421-21508432 chr9:21508423-21508431 chr9:21508423-21508432
46	FOS	chr9:21505493-21505766	MCF10A-Er-Src	breast:	n/a	n/a
47	FOS	chr9:21513417-21513900	MCF10A-Er-Src	breast:	n/a	n/a
48	FOSL1	chr9:21506525-21507527	HCT-116	colon:	n/a	chr9:21506578-21506590
49	FOSL1	chr9:21519573-21524793	HCT-116	colon:	n/a	n/a
50	FOSL1	chr9:21505232-21505921	HCT-116	colon:	n/a	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr11:61583818..61584553-chr9:21518322..21519322,2	HCT-116	colon:
2	chr14:68668658..68669180-chr9:21520044..21520625,2	HCT-116	colon:

miRNA name	Chromosome Location	mirBase accession
hsa-miR-31-3p	chr9:21512120-21512141	MIMAT0004504
hsa-miR-31-5p	chr9:21512157-21512177	MIMAT0000089

Variant related genes	Relation type
MIR31	TF binding region
ENSG00000264379	TF binding region
ENSG00000134824	chromatin interactions
ENSG00000149485	chromatin interactions
JAZF1	Mature miRNA region
MPRIP	Mature miRNA region
CYP27B1	Mature miRNA region
HEATR2	Mature miRNA region
CIPC	Mature miRNA region
SFXN1	Mature miRNA region
TNKS2	Mature miRNA region
DACT3	Mature miRNA region
PPP2R5C	Mature miRNA region
XK	Mature miRNA region
ITGA5	Mature miRNA region
INHBA	Mature miRNA region
MYO1D	Mature miRNA region
PTPRJ	Mature miRNA region
RET	Mature miRNA region
C2CD5	Mature miRNA region
HIST1H2BI	Mature miRNA region
RANGAP1	Mature miRNA region
RASA1	Mature miRNA region
RICTOR	Mature miRNA region
DKK1	Mature miRNA region
HOXA7	Mature miRNA region
UBA6	Mature miRNA region
SATB2	Mature miRNA region
ARL6IP5	Mature miRNA region
ETS1	Mature miRNA region
CREG1	Mature miRNA region
HOXC13	Mature miRNA region
MED12	Mature miRNA region
DNAJC5	Mature miRNA region
DDX19A	Mature miRNA region
CDK1	Mature miRNA region
NFATC2IP	Mature miRNA region
EDC3	Mature miRNA region
PRKCE	Mature miRNA region
ZNF275	Mature miRNA region
SRRM2	Mature miRNA region
PPIL2	Mature miRNA region
STOML2	Mature miRNA region
SELE	Mature miRNA region
RHOA	Mature miRNA region
AKAP8L	Mature miRNA region
PPP2R2A	Mature miRNA region
CASR	Mature miRNA region
MET	Mature miRNA region
RPL37A	Mature miRNA region
EXOSC5	Mature miRNA region
ACADVL	Mature miRNA region
NFAT5	Mature miRNA region
MMP16	Mature miRNA region
KLF13	Mature miRNA region
MLH1	Mature miRNA region
NOL9	Mature miRNA region
HIST1H2BJ	Mature miRNA region
FZD3	Mature miRNA region
ZC3H12C	Mature miRNA region
ARPC5	Mature miRNA region
PPIA	Mature miRNA region
RPS4Y1	Mature miRNA region
NDFIP2	Mature miRNA region
SLC9A6	Mature miRNA region
RPA1	Mature miRNA region
ILF2	Mature miRNA region
DMD	Mature miRNA region
FOXP3	Mature miRNA region
TXNDC5	Mature miRNA region
TRIB3	Mature miRNA region
NUS1	Mature miRNA region
RPS7	Mature miRNA region
ATP2A2	Mature miRNA region
PCSK1N	Mature miRNA region
GLI2	Mature miRNA region
FLNA	Mature miRNA region
YY1	Mature miRNA region
DBR1	Mature miRNA region
TRRAP	Mature miRNA region
STK40	Mature miRNA region
GYG1	Mature miRNA region
FAM134C	Mature miRNA region
HIF1AN	Mature miRNA region
MCM2	Mature miRNA region
LATS2	Mature miRNA region
NUP188	Mature miRNA region
ZC3H18	Mature miRNA region
LRRC59	Mature miRNA region
C1orf198	Mature miRNA region
SMEK2	Mature miRNA region
HIST1H2BK	Mature miRNA region
MCM4	Mature miRNA region
NUMB	Mature miRNA region
TNRC6B	Mature miRNA region
PEX19	Mature miRNA region
CXCL12	Mature miRNA region
GHITM	Mature miRNA region
ICAM1	Mature miRNA region
EXOC6	Mature miRNA region
RDX	Mature miRNA region
NOP56	Mature miRNA region
TIAM1	Mature miRNA region
AGO1	Mature miRNA region
RAN	Mature miRNA region

Extended variants
information (count: 1167 )
Associated
traits (count: 154 )

Variant overlapped rSNPs/rCNVs (count:1167 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7849420	chr9:21499624-21499625	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	disease
2	rs536393758	chr9:21499653-21499654	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs548758819	chr9:21499689-21499690	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs185302550	chr9:21499751-21499752	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs7849575	chr9:21499793-21499794	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs9696745	chr9:21499817-21499818	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs577893076	chr9:21499818-21499819	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs112274556	chr9:21499825-21499826	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs564738565	chr9:21499838-21499839	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs78266431	chr9:21499852-21499853	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs190063040	chr9:21499892-21499893	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs372519854	chr9:21499912-21499913	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs547469365	chr9:21499928-21499929	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs573669853	chr9:21499936-21499937	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs149996492	chr9:21499960-21499961	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs563027792	chr9:21499980-21499981	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs576733554	chr9:21499992-21499993	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs369603500	chr9:21499998-21499999	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs183220995	chr9:21500024-21500025	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs376846537	chr9:21500052-21500053	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs187784141	chr9:21500088-21500089	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs192461544	chr9:21500101-21500102	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs537321692	chr9:21500109-21500110	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs565726775	chr9:21500113-21500114	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs561167447	chr9:21500115-21500116	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs58021384	chr9:21500200-21500201	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs549884261	chr9:21500204-21500205	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs149174200	chr9:21500216-21500217	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs183914773	chr9:21500248-21500249	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs551189238	chr9:21500255-21500256	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs536246234	chr9:21500258-21500259	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs571513040	chr9:21500277-21500278	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs187992830	chr9:21500287-21500288	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs191979583	chr9:21500293-21500294	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs143330593	chr9:21500300-21500301	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs184579261	chr9:21500322-21500323	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs556312382	chr9:21500339-21500340	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs148343958	chr9:21500363-21500364	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs561150969	chr9:21500371-21500372	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs141766298	chr9:21500403-21500404	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs189239327	chr9:21500416-21500417	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs12004228	chr9:21500433-21500434	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs111813561	chr9:21500443-21500444	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs541370864	chr9:21500453-21500454	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs576267512	chr9:21500479-21500480	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs191696203	chr9:21500523-21500524	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs530050478	chr9:21500531-21500532	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs147103457	chr9:21500588-21500589	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs113559909	chr9:21500607-21500608	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs563419734	chr9:21500625-21500626	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:154)

Disease	PMID	Source
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
Oral squamous cell carcinoma	17134496	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
Chronic lymphocytic leukemia	21546498	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
microdeletion syndrome	16199537	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Cancer	20164919	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
Chronic myeloid leukemia	21384125	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
Malignant peripheral nerve sheath tumor	18522746	CNVD
Non-small cell lung cancer	19010865	CNVD
Myoepithelioma	18604193	CNVD
Cancer	22183965	CNVD
Glioblastoma multiforme	21569311	CNVD
Myelofibrosis	22110671	CNVD
Ewing''s sarcoma	22429812	CNVD
Neuroblastoma	21899760	CNVD
Glioblastoma multiforme	19435819	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Glioblastoma multiforme	22291905	CNVD
Lung cancer	21911935	CNVD
Primary central nervous system lymphoma	21088137	CNVD
head and neck squamous cell carcinoma	21798897	CNVD
Cancer	21253487	CNVD
Glioblastoma multiforme	22286061	CNVD
Intracranial ependymoma	16609018	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Glioblastoma multiforme	21922591	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Urothelial cell carcinoma	18451213	CNVD
Glioma	17123091	CNVD
Mental retardation	17124404	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Acute lymphoblastic leukemia	18768390	CNVD
Leukemia	19602459	CNVD
Acute monocytic leukemia	16498392	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Leukemia	18688285	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Acute myeloid leukemia	19651601	CNVD
Coronary Disease	20032323	CNVD
Squamous cell cancer	20885788	CNVD
Hirschsprung''s Disease	21712996	CNVD
Cancer	21732550	CNVD
Gastric cancer	22539939	CNVD
Cancer	21183584	CNVD
T-cell lymphomas	19863542	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Metastatic melanoma	18483359	CNVD
Non-small cell lung cancer	20864512	CNVD
Cervical cancer	21062161	CNVD
Acute myeloid leukemia	16864856	CNVD
Glioblastoma	17090523	CNVD
Lung cancer	16773561	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Colorectal cancer	16774939	CNVD
Bladder cancer	19088036	CNVD
Colorectal cancer	16272173	CNVD
Melanoma	16977458	CNVD
Glioblastoma multiforme	17369134	CNVD
Chagasic megaesophagus	20163722	CNVD
Melanoma	19566914	CNVD
Squamous cell cancer	19047905	CNVD
Lung adenocarcinoma	19525976	CNVD
Lung cancer	19525976	CNVD
Hodgkin''s lymphoma	18179710	CNVD
Glioma	20126413	CNVD
Melanoma	17363583	CNVD
Glioblastoma multiforme	19115005	CNVD
Glioblastoma multiforme	21525872	CNVD
Glioblastoma multiforme	21138945	CNVD
Adenoid cystic carcinoma	18332873	CNVD
Breast cancer	21364760	CNVD
Cancer	20581869	CNVD
Multiple myeloma	17550852	CNVD
Oral cancer	22144094	CNVD
Lung cancer	21569311	CNVD
Epilepsy	20502679	CNVD
Barrett''s syndrome	19417022	CNVD
Pancreatic cancer	21811587	CNVD
Breast cancer	22522925	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD
Cancer	20164920	CNVD
Non-small cell lung cancer	16651412	CNVD

Chromatin state (count:344 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:21463000-21502200	Weak transcription	HSMM	muscle
2	chr9:21466000-21527600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr9:21471600-21505600	Weak transcription	HUVEC	blood vessel
4	chr9:21477000-21505800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
5	chr9:21479600-21505000	Weak transcription	NHLF	lung
6	chr9:21481800-21500000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
7	chr9:21481800-21504800	Weak transcription	NHDF-Ad	bronchial
8	chr9:21481800-21505000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
9	chr9:21482000-21504800	Weak transcription	NHEK	skin
10	chr9:21483200-21501200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
11	chr9:21483200-21502200	Weak transcription	Muscle Satellite Cultured Cells	--
12	chr9:21483200-21504800	Weak transcription	HMEC	breast
13	chr9:21487200-21500600	Weak transcription	Osteobl	bone
14	chr9:21494200-21503600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr9:21494800-21527600	Weak transcription	Gastric	stomach
16	chr9:21497400-21500000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
17	chr9:21498200-21500000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
18	chr9:21498800-21500800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
19	chr9:21499000-21500800	Enhancers	A549	lung
20	chr9:21499200-21503600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
21	chr9:21499400-21499800	Enhancers	Fetal Intestine Small	intestine
22	chr9:21499400-21500200	Weak transcription	Stomach Mucosa	stomach
23	chr9:21499800-21500000	Weak transcription	Fetal Intestine Small	intestine
24	chr9:21500000-21500200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
25	chr9:21500000-21500800	Enhancers	Fetal Intestine Small	intestine
26	chr9:21500000-21501000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
27	chr9:21500000-21503000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
28	chr9:21500200-21500600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
29	chr9:21500200-21500800	Enhancers	NH-A	brain
30	chr9:21500200-21501000	Enhancers	Stomach Mucosa	stomach
31	chr9:21500400-21501000	Enhancers	Duodenum Mucosa	Duodenum
32	chr9:21500600-21500800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
33	chr9:21500600-21502200	Enhancers	Osteobl	bone
34	chr9:21500800-21501200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
35	chr9:21500800-21501400	Enhancers	Breast Myoepithelial Primary Cells	Breast
36	chr9:21500800-21501400	Genic enhancers	A549	lung
37	chr9:21500800-21504800	Weak transcription	NH-A	brain
38	chr9:21500800-21505000	Weak transcription	Fetal Intestine Small	intestine
39	chr9:21500800-21505200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
40	chr9:21501000-21503800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
41	chr9:21501000-21505400	Weak transcription	Stomach Mucosa	stomach
42	chr9:21501000-21505800	Weak transcription	Duodenum Mucosa	Duodenum
43	chr9:21501200-21503200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
44	chr9:21501400-21502200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
45	chr9:21501400-21504600	Weak transcription	A549	lung
46	chr9:21502200-21502400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr9:21502200-21502400	Enhancers	Placenta	Placenta
48	chr9:21502200-21502600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr9:21502200-21502800	Enhancers	HSMM	muscle
50	chr9:21502200-21503000	Enhancers	Breast Myoepithelial Primary Cells	Breast

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