Variant report

Variant	esv3439842
Chromosome Location	chr9:21186801-21227493
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:427)
CpG islands
(count:122)
Chromatin interactive
region (count:0)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:427 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BATF	chr9:21195452-21195727	GM12878	blood:	n/a	n/a
2	BATF	chr9:21214009-21214242	GM12878	blood:	n/a	n/a
3	BATF	chr9:21213980-21214258	GM12878	blood:	n/a	n/a
4	BATF	chr9:21195481-21195714	GM12878	blood:	n/a	n/a
5	BCL11A	chr9:21195389-21195749	GM12878	blood:	n/a	chr9:21195583-21195592
6	BCL11A	chr9:21195471-21195683	GM12878	blood:	n/a	chr9:21195583-21195592
7	BCL11A	chr9:21213999-21214266	GM12878	blood:	n/a	chr9:21214111-21214120
8	BCL11A	chr9:21213900-21214291	GM12878	blood:	n/a	chr9:21214111-21214120
9	BHLHE40	chr9:21195256-21195293	GM12878	blood:	n/a	n/a
10	CEBPB	chr9:21213807-21213921	IMR90	lung:	n/a	n/a
11	CTCF	chr9:21195260-21195410	AoAF	blood vessel:	n/a	chr9:21195318-21195336
12	CTCF	chr9:21195148-21195378	A549	lung:	n/a	chr9:21195318-21195336
13	CTCF	chr9:21195320-21195470	HMEC	breast:	n/a	n/a
14	CTCF	chr9:21195161-21195401	H1-hESC	embryonic stem cell:	n/a	chr9:21195318-21195336
15	CTCF	chr9:21195260-21195410	GM12865	blood:	n/a	chr9:21195318-21195336
16	CTCF	chr9:21213780-21213930	GM12871	blood:	n/a	n/a
17	CTCF	chr9:21213739-21213950	HepG2	liver:	n/a	n/a
18	CTCF	chr9:21195178-21195445	MCF-7	breast:	n/a	chr9:21195318-21195336
19	CTCF	chr9:21195187-21195435	HepG2	liver:	n/a	chr9:21195318-21195336
20	CTCF	chr9:21213760-21213910	GM12872	blood:	n/a	n/a
21	CTCF	chr9:21195220-21195370	AG04449	skin:	n/a	chr9:21195318-21195336
22	CTCF	chr9:21195240-21195390	GM12866	blood:	n/a	chr9:21195318-21195336
23	CTCF	chr9:21195260-21195410	GM12867	blood:	n/a	chr9:21195318-21195336
24	CTCF	chr9:21213803-21213903	GM20000	blood:	n/a	n/a
25	CTCF	chr9:21214078-21214115	GM10248	blood:	n/a	n/a
26	CTCF	chr9:21213660-21213810	WI-38	lung:	n/a	n/a
27	CTCF	chr9:21213778-21213915	MCF-7	breast:	n/a	n/a
28	CTCF	chr9:21213780-21213930	BE2_C	brain:	n/a	n/a
29	CTCF	chr9:21195140-21195290	GM06990	blood:	n/a	n/a
30	CTCF	chr9:21195195-21195415	GM20000	blood:	n/a	chr9:21195318-21195336
31	CTCF	chr9:21195140-21195290	HFF	foreskin:	n/a	n/a
32	CTCF	chr9:21195120-21195270	RPTEC	kidney:	n/a	n/a
33	CTCF	chr9:21195120-21195270	HEEpiC	esophagus:	n/a	n/a
34	CTCF	chr9:21195260-21195410	BE2_C	brain:	n/a	chr9:21195318-21195336
35	CTCF	chr9:21213760-21213910	GM12878	blood:	n/a	n/a
36	CTCF	chr9:21195186-21195422	MCF-7	breast:	n/a	chr9:21195318-21195336
37	CTCF	chr9:21195576-21195686	LNCaP	prostate:	n/a	n/a
38	CTCF	chr9:21195220-21195370	GM12872	blood:	n/a	chr9:21195318-21195336
39	CTCF	chr9:21213780-21213930	HEEpiC	esophagus:	n/a	n/a
40	CTCF	chr9:21195076-21195079	GM12891	blood:	n/a	n/a
41	CTCF	chr9:21195160-21195310	HVMF	connective:	n/a	n/a
42	CTCF	chr9:21195280-21195430	GM12872	blood:	n/a	chr9:21195318-21195336
43	CTCF	chr9:21195160-21195310	GM12873	blood:	n/a	n/a
44	CTCF	chr9:21213763-21213941	LNCaP	prostate:	n/a	n/a
45	CTCF	chr9:21213780-21213930	HUVEC	blood vessel:	n/a	n/a
46	CTCF	chr9:21195168-21195484	LNCaP	prostate:	n/a	chr9:21195318-21195336
47	CTCF	chr9:21195213-21195422	Kidney_OC	kidney:	n/a	chr9:21195318-21195336
48	CTCF	chr9:21195240-21195390	SAEC	small airway:	n/a	chr9:21195318-21195336
49	CTCF	chr9:21195204-21195429	GM13976	blood:	n/a	chr9:21195318-21195336
50	CTCF	chr9:21195140-21195290	NB4	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:21202213-21202263	AG09309	skin:	n/a
2	chr9:21187344-21187394	BJ	skin:	n/a
3	chr9:21187344-21187394	PFSK-1	brain:	n/a
4	chr9:21202213-21202263	ovcar-3	ovarian:	n/a
5	chr9:21202213-21202263	HUVEC	blood vessel:	n/a
6	chr9:21187344-21187394	AG09309	skin:	n/a
7	chr9:21202213-21202263	Jurkat	blood:	n/a
8	chr9:21187344-21187394	SKMC	muscle:	n/a
9	chr9:21187344-21187394	ovcar-3	ovarian:	n/a
10	chr9:21202213-21202263	PFSK-1	brain:	n/a
11	chr9:21202213-21202263	LNCaP	prostate:	n/a
12	chr9:21187344-21187394	T-47D	breast:	n/a
13	chr9:21187344-21187394	HRCEpiC	kidney:	n/a
14	chr9:21202213-21202263	NH-A	brain:	n/a
15	chr9:21202213-21202263	ECC-1	luminal epithelium:	n/a
16	chr9:21187344-21187394	A549	lung:	n/a
17	chr9:21187344-21187394	GM06990	blood:	n/a
18	chr9:21202213-21202263	K562	blood:	n/a
19	chr9:21202213-21202263	HCT-116	colon:	n/a
20	chr9:21187344-21187394	IMR90	lung:	fetal
21	chr9:21187344-21187394	NHDF-neo	bronchial:	n/a
22	chr9:21187344-21187394	MCF10A-Er-Src	breast:	n/a
23	chr9:21187344-21187394	HNPCEpiC	eye:	n/a
24	chr9:21202213-21202263	T-47D	breast:	n/a
25	chr9:21187344-21187394	ECC-1	luminal epithelium:	n/a
26	chr9:21202213-21202263	AoSMC	blood vessel:	n/a
27	chr9:21202213-21202263	AG04449	skin:	fetal
28	chr9:21202213-21202263	IMR90	lung:	fetal
29	chr9:21187344-21187394	AG10803	skin:	n/a
30	chr9:21202213-21202263	AG04450	lung:	fetal
31	chr9:21202213-21202263	NT2-D1	testis:	n/a
32	chr9:21187344-21187394	NB4	blood:	n/a
33	chr9:21187344-21187394	GM12878	blood:	n/a
34	chr9:21187344-21187394	Hepatocyte	liver:	n/a
35	chr9:21202213-21202263	GM12891	blood:	n/a
36	chr9:21202213-21202263	AG10803	skin:	n/a
37	chr9:21202213-21202263	HCM	heart:	n/a
38	chr9:21187344-21187394	K562	blood:	n/a
39	chr9:21187344-21187394	PANC-1	pancreas:	n/a
40	chr9:21202213-21202263	HEEpiC	esophagus:	n/a
41	chr9:21187344-21187394	AG04450	lung:	fetal
42	chr9:21202213-21202263	SK-N-MC	brain:	n/a
43	chr9:21187344-21187394	HL-60	blood:	n/a
44	chr9:21187344-21187394	SK-N-MC	brain:	n/a
45	chr9:21187344-21187394	HPAEpiC	pulmonary alveolar:	n/a
46	chr9:21202213-21202263	NHBE	bronchial:	n/a
47	chr9:21187344-21187394	U87	brain:	n/a
48	chr9:21202213-21202263	NB4	blood:	n/a
49	chr9:21202213-21202263	AG09319	gingival:	n/a
50	chr9:21202213-21202263	HPAEpiC	pulmonary alveolar:	n/a

No data

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-IFNA10-1	chr9:21209188-21209778	NONHSAT130374
2	lnc-IFNA4-1	chr9:21190653-21191243	NONHSAT130373

No data

Variant related genes	Relation type
IFNA7	TF binding region
IFNA10	TF binding region
IFNWP9	TF binding region
IFNWP18	TF binding region
IFNA16	TF binding region
IFNA4	TF binding region
IFNA7	CpG island
IFNA10	CpG island
IFNWP9	CpG island
IFNWP18	CpG island
IFNA16	CpG island
IFNA4	CpG island

Extended variants
information (count: 448 )
Associated
traits (count: 155 )

Variant overlapped rSNPs/rCNVs (count:448 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs548959781	chr9:21187600-21187601	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs569045849	chr9:21187618-21187619	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs186540230	chr9:21189514-21189515	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs559783311	chr9:21189551-21189552	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs192258233	chr9:21190676-21190677	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
6	rs566716719	chr9:21190713-21190714	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
7	rs377120876	chr9:21190728-21190729	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
8	rs3091295	chr9:21190742-21190743	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
9	rs528238591	chr9:21190746-21190747	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
10	rs182257992	chr9:21190781-21190782	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
11	rs3091294	chr9:21190827-21190828	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
12	rs201737199	chr9:21190832-21190833	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
13	rs3955236	chr9:21190833-21190834	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
14	rs397839768	chr9:21190839-21190840	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
15	rs531769598	chr9:21190842-21190843	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
16	rs186881884	chr9:21190860-21190861	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
17	rs570786054	chr9:21190880-21190881	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
18	rs539727682	chr9:21190907-21190908	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
19	rs553243035	chr9:21190924-21190925	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
20	rs572948363	chr9:21190938-21190939	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
21	rs191676827	chr9:21190964-21190965	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
22	rs555545701	chr9:21190974-21190975	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
23	rs575616134	chr9:21190997-21190998	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
24	rs3091292	chr9:21191016-21191017	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
25	rs3091291	chr9:21191017-21191018	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
26	rs3091290	chr9:21191035-21191036	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
27	rs397705769	chr9:21191038-21191039	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
28	rs564125037	chr9:21191054-21191055	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
29	rs577960019	chr9:21191094-21191095	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
30	rs540523869	chr9:21191112-21191113	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
31	rs560320070	chr9:21191117-21191118	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
32	rs529429484	chr9:21191147-21191148	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
33	rs376524950	chr9:21191155-21191156	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
34	rs28619950	chr9:21191169-21191170	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
35	rs4007646	chr9:21191199-21191200	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs568649538	chr9:21193339-21193340	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs10811497	chr9:21193432-21193433	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
38	rs549487642	chr9:21193434-21193435	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs569440651	chr9:21193435-21193436	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs538330947	chr9:21193438-21193439	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs150058539	chr9:21193482-21193483	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs10811498	chr9:21193502-21193503	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	mRNA abundance
43	rs10811499	chr9:21193511-21193512	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	mRNA abundance
44	rs535586655	chr9:21194721-21194722	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs10811501	chr9:21194730-21194731	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs386733477	chr9:21194976-21194977	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs10448163	chr9:21194978-21194979	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs530602000	chr9:21194979-21194980	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs6475510	chr9:21194988-21194989	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
50	rs189321987	chr9:21194995-21194996	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:155)

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
Glioblastoma multiforme	21525872	CNVD
Melanoma	17363583	CNVD
Glioblastoma multiforme	19115005	CNVD
Glioblastoma multiforme	21138945	CNVD
Adenoid cystic carcinoma	18332873	CNVD
Breast cancer	21364760	CNVD
Cancer	20581869	CNVD
XY gonadal dysgenesis	20685758	CNVD
Multiple myeloma	17550852	CNVD
Intellectual disability	22102821	CNVD
Oral cancer	22144094	CNVD
Lung cancer	21569311	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	19212409	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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