Variant report

Variant	nsv438097
Chromosome Location	chr9:21285389-21306318
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	ATF2	chr9:21295176-21295511	GM12878	blood:	n/a	n/a
2	BCL11A	chr9:21294961-21295244	GM12878	blood:	n/a	n/a
3	BCL11A	chr9:21295247-21295511	GM12878	blood:	n/a	n/a
4	BCL11A	chr9:21295273-21295487	GM12878	blood:	n/a	n/a
5	BHLHE40	chr9:21295038-21295518	GM12878	blood:	n/a	n/a
6	CBX3	chr9:21294177-21294800	HCT-116	colon:	n/a	n/a
7	CBX3	chr9:21294159-21294859	HCT-116	colon:	n/a	n/a
8	CEBPB	chr9:21294131-21294913	HCT-116	colon:	n/a	n/a
9	CEBPB	chr9:21294087-21295054	HCT-116	colon:	n/a	chr9:21294973-21294984
10	CEBPB	chr9:21294292-21294892	Hela-S3	cervix:	n/a	n/a
11	CHD2	chr9:21295023-21295452	GM12878	blood:	n/a	n/a
12	CHD2	chr9:21294296-21294681	Hela-S3	cervix:	n/a	n/a
13	CTCF	chr9:21300767-21300841	GM20000	blood:	n/a	n/a
14	CTCF	chr9:21289780-21289930	HFF	foreskin:	n/a	n/a
15	CTCF	chr9:21302450-21302489	GM10266	blood:	n/a	n/a
16	CTCF	chr9:21288676-21288707	Kidney_OC	kidney:	n/a	n/a
17	CUX1	chr9:21295238-21295438	GM12878	blood:	n/a	n/a
18	EBF1	chr9:21294348-21294561	GM12878	blood:	n/a	n/a
19	EBF1	chr9:21296293-21296300	GM12878	blood:	n/a	n/a
20	EBF1	chr9:21295018-21295535	GM12878	blood:	n/a	n/a
21	EP300	chr9:21294977-21295571	GM12878	blood:	n/a	chr9:21295183-21295197
22	EP300	chr9:21294307-21294789	Hela-S3	cervix:	n/a	chr9:21294431-21294440 chr9:21294715-21294729
23	EP300	chr9:21294963-21295587	GM12878	blood:	n/a	chr9:21295183-21295197
24	EP300	chr9:21294891-21295540	GM12878	blood:	n/a	chr9:21295183-21295197
25	FOS	chr9:21294256-21294636	MCF10A-Er-Src	breast:	n/a	chr9:21294485-21294496 chr9:21294431-21294440 chr9:21294431-21294438
26	FOS	chr9:21294312-21294611	HUVEC	blood vessel:	n/a	chr9:21294485-21294496 chr9:21294431-21294440 chr9:21294431-21294438
27	FOS	chr9:21294286-21294878	MCF10A-Er-Src	breast:	n/a	chr9:21294485-21294496 chr9:21294431-21294440 chr9:21294431-21294438
28	FOS	chr9:21294288-21294891	MCF10A-Er-Src	breast:	n/a	chr9:21294485-21294496 chr9:21294431-21294440 chr9:21294431-21294438
29	FOS	chr9:21294290-21294669	MCF10A-Er-Src	breast:	n/a	chr9:21294485-21294496 chr9:21294431-21294440 chr9:21294431-21294438
30	FOSL1	chr9:21293304-21293875	HCT-116	colon:	n/a	chr9:21293625-21293633 chr9:21293625-21293633 chr9:21293626-21293633
31	FOSL1	chr9:21294149-21294790	HCT-116	colon:	n/a	chr9:21294485-21294496 chr9:21294431-21294440 chr9:21294431-21294438
32	FOSL1	chr9:21294030-21294995	HCT-116	colon:	n/a	chr9:21294485-21294496 chr9:21294431-21294440 chr9:21294431-21294438
33	FOSL2	chr9:21294329-21294604	HepG2	liver:	n/a	chr9:21294485-21294496 chr9:21294431-21294440 chr9:21294431-21294438
34	FOSL2	chr9:21294261-21294651	MCF-7	breast:	n/a	chr9:21294485-21294496 chr9:21294431-21294440 chr9:21294431-21294438
35	GATA2	chr9:21289874-21290218	SH-SY5Y	brain:	n/a	chr9:21290053-21290063 chr9:21290053-21290062 chr9:21290050-21290066
36	GATA3	chr9:21289924-21290166	T-47D	breast:	n/a	chr9:21290053-21290063 chr9:21290053-21290062 chr9:21290054-21290062 chr9:21290050-21290066
37	IKZF1	chr9:21295093-21295574	GM12878	blood:	n/a	n/a
38	JUN	chr9:21294272-21294882	Hela-S3	cervix:	n/a	chr9:21294485-21294496 chr9:21294431-21294440 chr9:21294431-21294438
39	JUN	chr9:21294282-21294452	HepG2	liver:	n/a	chr9:21294431-21294440 chr9:21294431-21294438
40	JUND	chr9:21294116-21294817	HCT-116	colon:	n/a	chr9:21294485-21294496 chr9:21294431-21294440 chr9:21294431-21294438
41	JUND	chr9:21294239-21294930	Hela-S3	cervix:	n/a	chr9:21294485-21294496 chr9:21294431-21294440 chr9:21294431-21294438
42	JUND	chr9:21294175-21294900	HCT-116	colon:	n/a	chr9:21294485-21294496 chr9:21294431-21294440 chr9:21294431-21294438
43	JUND	chr9:21294316-21294488	HepG2	liver:	n/a	chr9:21294431-21294440 chr9:21294431-21294438
44	MAFF	chr9:21300706-21300972	HepG2	liver:	n/a	chr9:21300843-21300861
45	MAFK	chr9:21296257-21296312	HepG2	liver:	n/a	n/a
46	MAFK	chr9:21293565-21293652	HepG2	liver:	n/a	n/a
47	MAX	chr9:21294234-21294610	NB4	blood:	n/a	chr9:21294449-21294459
48	MAX	chr9:21294109-21294851	HCT-116	colon:	n/a	chr9:21294449-21294459
49	MAX	chr9:21304604-21304636	NB4	blood:	n/a	n/a
50	MAX	chr9:21294250-21294652	Hela-S3	cervix:	n/a	chr9:21294449-21294459

Variant related genes	Relation type
IFNA5	TF binding region

Extended variants
information (count: 581 )
Associated
traits (count: 153 )

Variant overlapped rSNPs/rCNVs (count:581 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1475547	chr9:21285389-21285390	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs553204570	chr9:21285420-21285421	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs548201522	chr9:21285477-21285478	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs149713445	chr9:21285542-21285543	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs369088012	chr9:21285546-21285547	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs536951826	chr9:21285553-21285554	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs558598398	chr9:21285615-21285616	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs570572596	chr9:21285621-21285622	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs185398994	chr9:21285658-21285659	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs553080183	chr9:21285793-21285794	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs572999148	chr9:21285825-21285826	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs545799690	chr9:21285828-21285829	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs145582647	chr9:21285833-21285834	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs555352031	chr9:21285835-21285836	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs542081081	chr9:21285838-21285839	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs187918065	chr9:21285869-21285870	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs200661056	chr9:21285908-21285909	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs544598856	chr9:21285934-21285935	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs192942842	chr9:21286027-21286028	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs184195478	chr9:21286037-21286038	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs74635289	chr9:21286070-21286071	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs559534204	chr9:21286071-21286072	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs10964958	chr9:21286078-21286079	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
24	rs548262289	chr9:21286085-21286086	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs561553952	chr9:21286140-21286141	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs148902262	chr9:21286143-21286144	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs550637313	chr9:21286162-21286163	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs115579813	chr9:21286191-21286192	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs539296950	chr9:21286196-21286197	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs188294479	chr9:21286204-21286205	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs566290656	chr9:21286208-21286209	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs181795491	chr9:21286221-21286222	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs555413425	chr9:21286223-21286224	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs575563817	chr9:21286225-21286226	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs539892407	chr9:21286229-21286230	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs538221173	chr9:21286232-21286233	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs560322065	chr9:21286236-21286237	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs112915348	chr9:21286254-21286255	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs7020867	chr9:21286288-21286289	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
40	rs147011308	chr9:21286292-21286293	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs540867221	chr9:21286299-21286300	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs560674417	chr9:21286303-21286304	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs76127293	chr9:21286304-21286305	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs541964641	chr9:21286325-21286326	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs184871262	chr9:21286327-21286328	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs78503390	chr9:21286338-21286339	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs555318567	chr9:21286364-21286365	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs564265652	chr9:21286367-21286368	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs533067668	chr9:21286376-21286377	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs546443477	chr9:21286399-21286400	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:153)

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
Intellectual disability	22102821	CNVD
Oral cancer	22144094	CNVD
Lung cancer	21569311	CNVD
Epilepsy	20502679	CNVD
Barrett''s syndrome	19417022	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD

Chromatin state (count:54 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:21282000-21286600	Weak transcription	Primary neutrophils fromperipheralblood	blood
2	chr9:21282000-21286800	Weak transcription	Monocytes-CD14+_RO01746	blood
3	chr9:21285000-21287400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr9:21286600-21287000	Enhancers	Primary neutrophils fromperipheralblood	blood
5	chr9:21286600-21289000	Enhancers	Primary monocytes fromperipheralblood	blood
6	chr9:21286800-21288000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
7	chr9:21287000-21287400	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
8	chr9:21287200-21288000	Enhancers	Primary hematopoietic stem cells short term culture	blood
9	chr9:21287400-21287600	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
10	chr9:21287400-21289200	Enhancers	Primary neutrophils fromperipheralblood	blood
11	chr9:21287600-21287800	Enhancers	Primary B cells from cord blood	blood
12	chr9:21287800-21288600	Weak transcription	Primary B cells from cord blood	blood
13	chr9:21288000-21288400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
14	chr9:21288000-21289000	Enhancers	Monocytes-CD14+_RO01746	blood
15	chr9:21288400-21289200	Enhancers	Primary hematopoietic stem cells short term culture	blood
16	chr9:21288800-21289000	Enhancers	Primary B cells from cord blood	blood
17	chr9:21289200-21289600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
18	chr9:21289600-21290200	Enhancers	Primary hematopoietic stem cells short term culture	blood
19	chr9:21289600-21290200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
20	chr9:21289600-21290200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr9:21289800-21290200	Bivalent Enhancer	Dnd41	blood
22	chr9:21290200-21294400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
23	chr9:21290200-21294800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr9:21293600-21294400	Enhancers	GM12878-XiMat	blood
25	chr9:21293600-21295200	Enhancers	HMEC	breast
26	chr9:21293800-21295400	Enhancers	Hela-S3	cervix
27	chr9:21294000-21295400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
28	chr9:21294200-21295000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr9:21294200-21295000	Enhancers	NHEK	skin
30	chr9:21294200-21295200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
31	chr9:21294400-21294800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
32	chr9:21294400-21294800	Bivalent Enhancer	A549	lung
33	chr9:21294400-21295200	Flanking Active TSS	GM12878-XiMat	blood
34	chr9:21294400-21295400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
35	chr9:21294400-21296800	Enhancers	Primary hematopoietic stem cells short term culture	blood
36	chr9:21294400-21297000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
37	chr9:21294600-21295600	Bivalent Enhancer	Primary B cells from cord blood	blood
38	chr9:21294800-21296600	Enhancers	Primary hematopoietic stem cells	blood
39	chr9:21294800-21296600	Enhancers	Monocytes-CD14+_RO01746	blood
40	chr9:21294800-21296800	Enhancers	Primary monocytes fromperipheralblood	blood
41	chr9:21294800-21296800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr9:21295000-21296400	Enhancers	Primary neutrophils fromperipheralblood	blood
43	chr9:21295200-21295800	Enhancers	Duodenum Smooth Muscle	Duodenum
44	chr9:21295200-21296000	Enhancers	GM12878-XiMat	blood
45	chr9:21295400-21295600	Bivalent Enhancer	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
46	chr9:21295400-21295800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
47	chr9:21295400-21295800	Enhancers	Primary B cells from peripheral blood	blood
48	chr9:21295800-21296200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
49	chr9:21296000-21296400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
50	chr9:21296000-21296400	Enhancers	Fetal Muscle Trunk	muscle

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