Variant report

Variant	esv3393912
Chromosome Location	chr9:21192898-21211563
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	chr9:21195481-21195714	GM12878	blood:	n/a	n/a
2	BATF	chr9:21195452-21195727	GM12878	blood:	n/a	n/a
3	BCL11A	chr9:21195471-21195683	GM12878	blood:	n/a	chr9:21195583-21195592
4	BCL11A	chr9:21195389-21195749	GM12878	blood:	n/a	chr9:21195583-21195592
5	BHLHE40	chr9:21195256-21195293	GM12878	blood:	n/a	n/a
6	CTCF	chr9:21195260-21195410	GM06990	blood:	n/a	chr9:21195318-21195336
7	CTCF	chr9:21195574-21195676	Lung_OC	lung:	n/a	n/a
8	CTCF	chr9:21195213-21195356	MCF-7	breast:	n/a	chr9:21195318-21195336
9	CTCF	chr9:21195260-21195410	HEEpiC	esophagus:	n/a	chr9:21195318-21195336
10	CTCF	chr9:21195240-21195390	GM12870	blood:	n/a	chr9:21195318-21195336
11	CTCF	chr9:21195220-21195370	GM12801	blood:	n/a	chr9:21195318-21195336
12	CTCF	chr9:21195220-21195370	GM12872	blood:	n/a	chr9:21195318-21195336
13	CTCF	chr9:21195340-21195490	RPTEC	kidney:	n/a	n/a
14	CTCF	chr9:21195203-21195371	MCF-7	breast:	n/a	chr9:21195318-21195336
15	CTCF	chr9:21195240-21195390	GM12864	blood:	n/a	chr9:21195318-21195336
16	CTCF	chr9:21195120-21195270	HAc	cerebellar:	n/a	n/a
17	CTCF	chr9:21195260-21195410	AG04450	lung:	n/a	chr9:21195318-21195336
18	CTCF	chr9:21195180-21195330	GM12874	blood:	n/a	n/a
19	CTCF	chr9:21195140-21195290	HPF	lung:	n/a	n/a
20	CTCF	chr9:21195822-21195909	GM10248	blood:	n/a	n/a
21	CTCF	chr9:21195222-21195424	HepG2	liver:	n/a	chr9:21195318-21195336
22	CTCF	chr9:21195260-21195410	BJ	skin:	n/a	chr9:21195318-21195336
23	CTCF	chr9:21206793-21206835	Pancreas_OC	pancreas:	n/a	n/a
24	CTCF	chr9:21195120-21195270	HVMF	connective:	n/a	n/a
25	CTCF	chr9:21195260-21195410	GM12867	blood:	n/a	chr9:21195318-21195336
26	CTCF	chr9:21195260-21195410	HEK293	kidney:	n/a	chr9:21195318-21195336
27	CTCF	chr9:21195120-21195270	HEEpiC	esophagus:	n/a	n/a
28	CTCF	chr9:21195300-21195450	GM12864	blood:	n/a	chr9:21195318-21195336
29	CTCF	chr9:21195148-21195378	A549	lung:	n/a	chr9:21195318-21195336
30	CTCF	chr9:21195031-21195042	GM19240	blood:	n/a	n/a
31	CTCF	chr9:21195160-21195310	GM12872	blood:	n/a	n/a
32	CTCF	chr9:21195340-21195490	HFF-Myc	foreskin:	n/a	n/a
33	CTCF	chr9:21195585-21195687	GM10266	blood:	n/a	n/a
34	CTCF	chr9:21195076-21195079	GM12891	blood:	n/a	n/a
35	CTCF	chr9:21195220-21195370	HL-60	blood:	n/a	chr9:21195318-21195336
36	CTCF	chr9:21195140-21195290	GM06990	blood:	n/a	n/a
37	CTCF	chr9:21195237-21195359	SK-N-SH_RA	brain:	n/a	chr9:21195318-21195336
38	CTCF	chr9:21195120-21195270	HA-sp	spinal cord:	n/a	n/a
39	CTCF	chr9:21194924-21195031	LNCaP	prostate:	n/a	n/a
40	CTCF	chr9:21195280-21195430	SK-N-SH_RA	brain:	n/a	chr9:21195318-21195336
41	CTCF	chr9:21195240-21195390	AG04450	lung:	n/a	chr9:21195318-21195336
42	CTCF	chr9:21195280-21195430	Caco-2	colon:	n/a	chr9:21195318-21195336
43	CTCF	chr9:21195240-21195390	GM12867	blood:	n/a	chr9:21195318-21195336
44	CTCF	chr9:21201815-21201948	GM10266	blood:	n/a	n/a
45	CTCF	chr9:21195140-21195290	NB4	blood:	n/a	n/a
46	CTCF	chr9:21195120-21195270	GM12869	blood:	n/a	n/a
47	CTCF	chr9:21195120-21195270	HFF-Myc	foreskin:	n/a	n/a
48	CTCF	chr9:21195240-21195390	HCPEpiC	choroid plexus:	n/a	chr9:21195318-21195336
49	CTCF	chr9:21195179-21195510	HUVEC	blood vessel:	n/a	chr9:21195318-21195336
50	CTCF	chr9:21195260-21195410	HA-sp	spinal cord:	n/a	chr9:21195318-21195336

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:21202213-21202263	LNCaP	prostate:	n/a
2	chr9:21202213-21202263	HCF	heart:	n/a
3	chr9:21202213-21202263	PrEC	prostate:	n/a
4	chr9:21202213-21202263	BE2_C	brain:	n/a
5	chr9:21202213-21202263	NB4	blood:	n/a
6	chr9:21202213-21202263	HMEC	breast:	n/a
7	chr9:21202213-21202263	GM12892	blood:	n/a
8	chr9:21202213-21202263	AG04450	lung:	fetal
9	chr9:21202213-21202263	A549	lung:	n/a
10	chr9:21202213-21202263	H1-hESC	embryonic stem cell:	embryo
11	chr9:21202213-21202263	AG09319	gingival:	n/a
12	chr9:21202213-21202263	MCF-7	breast:	n/a
13	chr9:21202213-21202263	HPAEpiC	pulmonary alveolar:	n/a
14	chr9:21202213-21202263	HepG2	liver:	n/a
15	chr9:21202213-21202263	HUVEC	blood vessel:	n/a
16	chr9:21202213-21202263	NHBE	bronchial:	n/a
17	chr9:21202213-21202263	HRE	kidney:	n/a
18	chr9:21202213-21202263	Caco-2	colon:	n/a
19	chr9:21202213-21202263	BJ	skin:	n/a
20	chr9:21202213-21202263	AoSMC	blood vessel:	n/a
21	chr9:21202213-21202263	K562	blood:	n/a
22	chr9:21202213-21202263	HEK293	kidney:	embryo
23	chr9:21202213-21202263	NHDF-neo	bronchial:	n/a
24	chr9:21202213-21202263	HCT-116	colon:	n/a
25	chr9:21202213-21202263	HNPCEpiC	eye:	n/a
26	chr9:21202213-21202263	NT2-D1	testis:	n/a
27	chr9:21202213-21202263	SAEC	small airway:	n/a
28	chr9:21202213-21202263	SK-N-MC	brain:	n/a
29	chr9:21202213-21202263	AG10803	skin:	n/a
30	chr9:21202213-21202263	HCM	heart:	n/a
31	chr9:21202213-21202263	Hepatocyte	liver:	n/a
32	chr9:21202213-21202263	HEEpiC	esophagus:	n/a
33	chr9:21202213-21202263	Jurkat	blood:	n/a
34	chr9:21202213-21202263	GM19239	blood:	n/a
35	chr9:21202213-21202263	RPTEC	kidney:	n/a
36	chr9:21202213-21202263	HCPEpiC	choroid plexus:	n/a
37	chr9:21202213-21202263	T-47D	breast:	n/a
38	chr9:21202213-21202263	GM12878	blood:	n/a
39	chr9:21202213-21202263	PANC-1	pancreas:	n/a
40	chr9:21202213-21202263	HRCEpiC	kidney:	n/a
41	chr9:21202213-21202263	ProgFib	skin:	n/a
42	chr9:21202213-21202263	HIPEpiC	eye:	n/a
43	chr9:21202213-21202263	IMR90	lung:	fetal
44	chr9:21202213-21202263	AG04449	skin:	fetal
45	chr9:21202213-21202263	ECC-1	luminal epithelium:	n/a
46	chr9:21202213-21202263	PFSK-1	brain:	n/a
47	chr9:21202213-21202263	SKMC	muscle:	n/a
48	chr9:21202213-21202263	GM06990	blood:	n/a
49	chr9:21202213-21202263	ovcar-3	ovarian:	n/a
50	chr9:21202213-21202263	U87	brain:	n/a

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-IFNA10-1	chr9:21209188-21209778	NONHSAT130374

Variant related genes	Relation type
IFNA7	TF binding region
IFNA10	TF binding region
IFNWP9	TF binding region
IFNWP18	TF binding region
IFNA7	CpG island
IFNA10	CpG island
IFNWP9	CpG island
IFNWP18	CpG island

Extended variants
information (count: 298 )
Associated
traits (count: 154 )

Variant overlapped rSNPs/rCNVs (count:298 , 50 per page) page: 1 2 3 4 5 6

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs568649538	chr9:21193339-21193340	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs10811497	chr9:21193432-21193433	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
3	rs549487642	chr9:21193434-21193435	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs569440651	chr9:21193435-21193436	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs538330947	chr9:21193438-21193439	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs150058539	chr9:21193482-21193483	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs10811498	chr9:21193502-21193503	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	mRNA abundance
8	rs10811499	chr9:21193511-21193512	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	mRNA abundance
9	rs535586655	chr9:21194721-21194722	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs10811501	chr9:21194730-21194731	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs386733477	chr9:21194976-21194977	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs10448163	chr9:21194978-21194979	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs530602000	chr9:21194979-21194980	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs6475510	chr9:21194988-21194989	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
15	rs189321987	chr9:21194995-21194996	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs10448164	chr9:21194998-21194999	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs533123020	chr9:21195039-21195040	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs546826389	chr9:21195041-21195042	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs566564406	chr9:21195051-21195052	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs192330192	chr9:21195098-21195099	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs184668005	chr9:21195099-21195100	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs111813733	chr9:21195100-21195101	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs373873286	chr9:21195117-21195118	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs143934548	chr9:21195132-21195133	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs146416077	chr9:21195134-21195135	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs12002880	chr9:21195135-21195136	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs551608506	chr9:21195151-21195152	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs376881784	chr9:21195158-21195159	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs534237515	chr9:21195246-21195247	Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs554415377	chr9:21195258-21195259	Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs367955998	chr9:21195265-21195266	Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs370948041	chr9:21195276-21195277	Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs200230006	chr9:21195278-21195279	Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs189281193	chr9:21195359-21195360	Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs62558983	chr9:21195373-21195374	Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs556781313	chr9:21195403-21195404	Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs181986903	chr9:21195414-21195415	Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs62558984	chr9:21195420-21195421	Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs76207521	chr9:21195438-21195439	Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs565793626	chr9:21195475-21195476	Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs544321369	chr9:21195489-21195490	Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs563929862	chr9:21195520-21195521	Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs577531191	chr9:21195533-21195534	Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs540179536	chr9:21195545-21195546	Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs535996110	chr9:21195644-21195645	Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs560424214	chr9:21195650-21195651	Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs529135681	chr9:21195659-21195660	Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs143849597	chr9:21195694-21195695	Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs373081991	chr9:21195695-21195696	Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs113338585	chr9:21195706-21195707	Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	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
Intellectual disability	22102821	CNVD
Oral cancer	22144094	CNVD
Lung cancer	21569311	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	19212409	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD
Epilepsy	20502679	CNVD
Barrett''s syndrome	19417022	CNVD

Chromatin state (count:16 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:21195200-21195600	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
2	chr9:21195200-21195800	Active TSS	Hela-S3	cervix
3	chr9:21195200-21196000	Enhancers	Primary neutrophils fromperipheralblood	blood
4	chr9:21195200-21196000	Enhancers	Monocytes-CD14+_RO01746	blood
5	chr9:21195400-21195800	Enhancers	Primary hematopoietic stem cells	blood
6	chr9:21195600-21195800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr9:21195600-21196200	Enhancers	GM12878-XiMat	blood
8	chr9:21195600-21196400	Enhancers	Primary monocytes fromperipheralblood	blood
9	chr9:21195800-21196000	Enhancers	Hela-S3	cervix
10	chr9:21196200-21196600	Weak transcription	GM12878-XiMat	blood
11	chr9:21196400-21197600	Weak transcription	Primary monocytes fromperipheralblood	blood
12	chr9:21196600-21197000	Enhancers	GM12878-XiMat	blood
13	chr9:21198000-21198200	Enhancers	Primary monocytes fromperipheralblood	blood
14	chr9:21198200-21198800	Enhancers	Placenta	Placenta
15	chr9:21211400-21211800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
16	chr9:21211400-21212200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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