Variant report

Variant	nsv892735
Chromosome Location	chr9:21157373-21242161
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	chr9:21214009-21214242	GM12878	blood:	n/a	n/a
2	BATF	chr9:21195452-21195727	GM12878	blood:	n/a	n/a
3	BATF	chr9:21183391-21183669	GM12878	blood:	n/a	n/a
4	BATF	chr9:21160171-21160535	GM12878	blood:	n/a	n/a
5	BATF	chr9:21183393-21183622	GM12878	blood:	n/a	n/a
6	BATF	chr9:21195481-21195714	GM12878	blood:	n/a	n/a
7	BATF	chr9:21160236-21160531	GM12878	blood:	n/a	n/a
8	BATF	chr9:21213980-21214258	GM12878	blood:	n/a	n/a
9	BATF	chr9:21236050-21236328	GM12878	blood:	n/a	n/a
10	BCL11A	chr9:21195389-21195749	GM12878	blood:	n/a	chr9:21195583-21195592
11	BCL11A	chr9:21236007-21236322	GM12878	blood:	n/a	chr9:21236181-21236190
12	BCL11A	chr9:21183431-21183637	GM12878	blood:	n/a	chr9:21183522-21183531
13	BCL11A	chr9:21213900-21214291	GM12878	blood:	n/a	chr9:21214111-21214120
14	BCL11A	chr9:21195471-21195683	GM12878	blood:	n/a	chr9:21195583-21195592
15	BCL11A	chr9:21236105-21236278	GM12878	blood:	n/a	chr9:21236181-21236190
16	BCL11A	chr9:21213999-21214266	GM12878	blood:	n/a	chr9:21214111-21214120
17	BHLHE40	chr9:21235842-21236001	GM12878	blood:	n/a	n/a
18	BHLHE40	chr9:21195256-21195293	GM12878	blood:	n/a	n/a
19	BRCA1	chr9:21235836-21236005	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr9:21235830-21236091	Hela-S3	cervix:	n/a	n/a
21	CEBPB	chr9:21176025-21176293	H1-hESC	embryonic stem cell:	n/a	chr9:21176156-21176169 chr9:21176156-21176169 chr9:21176158-21176167 chr9:21176233-21176244 chr9:21176231-21176244 chr9:21176156-21176167 chr9:21176157-21176168
22	CEBPB	chr9:21172249-21172496	A549	lung:	n/a	chr9:21172346-21172357
23	CEBPB	chr9:21172238-21172445	HepG2	liver:	n/a	chr9:21172346-21172357
24	CEBPB	chr9:21175996-21176312	HepG2	liver:	n/a	chr9:21176156-21176169 chr9:21176156-21176169 chr9:21176158-21176167 chr9:21176233-21176244 chr9:21176231-21176244 chr9:21176156-21176167 chr9:21176157-21176168
25	CEBPB	chr9:21175999-21176288	IMR90	lung:	n/a	chr9:21176156-21176169 chr9:21176156-21176169 chr9:21176158-21176167 chr9:21176233-21176244 chr9:21176231-21176244 chr9:21176156-21176167 chr9:21176157-21176168
26	CEBPB	chr9:21213807-21213921	IMR90	lung:	n/a	n/a
27	CEBPB	chr9:21183206-21183372	A549	lung:	n/a	n/a
28	CEBPB	chr9:21176035-21176261	A549	lung:	n/a	chr9:21176156-21176169 chr9:21176156-21176169 chr9:21176158-21176167 chr9:21176233-21176244 chr9:21176231-21176244 chr9:21176156-21176167 chr9:21176157-21176168
29	CTCF	chr9:21235793-21236036	Hela-S3	cervix:	n/a	chr9:21235917-21235938
30	CTCF	chr9:21235830-21236030	Kidney_OC	kidney:	n/a	chr9:21235917-21235938
31	CTCF	chr9:21183200-21183350	GM12872	blood:	n/a	chr9:21183259-21183277
32	CTCF	chr9:21235818-21236010	ECC-1	luminal epithelium:	n/a	chr9:21235917-21235938
33	CTCF	chr9:21183150-21183374	Lung_OC	lung:	n/a	chr9:21183259-21183277
34	CTCF	chr9:21213700-21213850	GM12870	blood:	n/a	n/a
35	CTCF	chr9:21213678-21214043	A549	lung:	n/a	n/a
36	CTCF	chr9:21183180-21183330	HEEpiC	esophagus:	n/a	chr9:21183259-21183277
37	CTCF	chr9:21195300-21195450	GM12869	blood:	n/a	chr9:21195318-21195336
38	CTCF	chr9:21195207-21195448	Lung_OC	lung:	n/a	chr9:21195318-21195336
39	CTCF	chr9:21195220-21195370	Hela-S3	cervix:	n/a	chr9:21195318-21195336
40	CTCF	chr9:21213700-21213850	GM12872	blood:	n/a	n/a
41	CTCF	chr9:21195280-21195430	HUVEC	blood vessel:	n/a	chr9:21195318-21195336
42	CTCF	chr9:21183127-21183381	LNCaP	prostate:	n/a	chr9:21183259-21183277
43	CTCF	chr9:21183060-21183210	GM12866	blood:	n/a	n/a
44	CTCF	chr9:21183200-21183350	SAEC	small airway:	n/a	chr9:21183259-21183277
45	CTCF	chr9:21213780-21213930	GM12871	blood:	n/a	n/a
46	CTCF	chr9:21213539-21213602	GM19240	blood:	n/a	n/a
47	CTCF	chr9:21235776-21236038	Gliobla	brain:	n/a	chr9:21235917-21235938
48	CTCF	chr9:21195260-21195410	AG09319	gingival:	n/a	chr9:21195318-21195336
49	CTCF	chr9:21195195-21195415	GM20000	blood:	n/a	chr9:21195318-21195336
50	CTCF	chr9:21213820-21213970	HL-60	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:21239944-21239994	SK-N-SH	brain:	n/a
2	chr9:21241233-21241283	NT2-D1	testis:	n/a
3	chr9:21239944-21239994	SK-N-SH	brain:	n/a
4	chr9:21241233-21241283	NT2-D1	testis:	n/a
5	chr9:21239944-21239994	AG04449	skin:	fetal
6	chr9:21202213-21202263	AG04450	lung:	fetal
7	chr9:21187344-21187394	HepG2	liver:	n/a
8	chr9:21241233-21241283	GM12892	blood:	n/a
9	chr9:21239944-21239994	HRPEpiC	eye:	n/a
10	chr9:21202213-21202263	AG10803	skin:	n/a
11	chr9:21239944-21239994	AG09319	gingival:	n/a
12	chr9:21187344-21187394	HEEpiC	esophagus:	n/a
13	chr9:21241233-21241283	Hepatocyte	liver:	n/a
14	chr9:21202213-21202263	A549	lung:	n/a
15	chr9:21239944-21239994	SKMC	muscle:	n/a
16	chr9:21202213-21202263	HIPEpiC	eye:	n/a
17	chr9:21187344-21187394	Hepatocyte	liver:	n/a
18	chr9:21239944-21239994	NHDF-neo	bronchial:	n/a
19	chr9:21241233-21241283	HAEpiC	amniotic membrane:	n/a
20	chr9:21239944-21239994	ProgFib	skin:	n/a
21	chr9:21241233-21241283	CMK	blood:	n/a
22	chr9:21187344-21187394	MCF10A-Er-Src	breast:	n/a
23	chr9:21241233-21241283	AG09309	skin:	n/a
24	chr9:21187344-21187394	ovcar-3	ovarian:	n/a
25	chr9:21239944-21239994	GM12892	blood:	n/a
26	chr9:21239944-21239994	CMK	blood:	n/a
27	chr9:21239944-21239994	SAEC	small airway:	n/a
28	chr9:21187344-21187394	MCF-7	breast:	n/a
29	chr9:21187344-21187394	SK-N-MC	brain:	n/a
30	chr9:21187344-21187394	AG09319	gingival:	n/a
31	chr9:21202213-21202263	GM12891	blood:	n/a
32	chr9:21187344-21187394	GM12878	blood:	n/a
33	chr9:21239944-21239994	AG09309	skin:	n/a
34	chr9:21202213-21202263	RPTEC	kidney:	n/a
35	chr9:21202213-21202263	SK-N-SH	brain:	n/a
36	chr9:21239944-21239994	HEEpiC	esophagus:	n/a
37	chr9:21241233-21241283	A549	lung:	n/a
38	chr9:21202213-21202263	HAEpiC	amniotic membrane:	n/a
39	chr9:21239944-21239994	HCT-116	colon:	n/a
40	chr9:21202213-21202263	U87	brain:	n/a
41	chr9:21187344-21187394	GM12891	blood:	n/a
42	chr9:21241233-21241283	NHDF-neo	bronchial:	n/a
43	chr9:21187344-21187394	HL-60	blood:	n/a
44	chr9:21241233-21241283	HIPEpiC	eye:	n/a
45	chr9:21202213-21202263	HRE	kidney:	n/a
46	chr9:21239944-21239994	HIPEpiC	eye:	n/a
47	chr9:21187344-21187394	ProgFib	skin:	n/a
48	chr9:21187344-21187394	RPTEC	kidney:	n/a
49	chr9:21241233-21241283	GM19239	blood:	n/a
50	chr9:21241233-21241283	HEEpiC	esophagus:	n/a

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-IFNA4-2	chr9:21178588-21179187	NONHSAT130372
2	lnc-IFNA10-1	chr9:21209188-21209778	NONHSAT130374
3	lnc-IFNA4-1	chr9:21190653-21191243	NONHSAT130373
4	lnc-IFNA17-1	chr9:21231265-21231852	NONHSAT130375

Variant related genes	Relation type
ENSG00000199635	TF binding region
IFNA7	TF binding region
IFNA21	TF binding region
IFNWP15	TF binding region
IFNWP9	TF binding region
IFNA14	TF binding region
IFNA17	TF binding region
IFNWP18	TF binding region
IFNA16	TF binding region
IFNA4	TF binding region
IFNA10	TF binding region
IFNWP5	TF binding region
ENSG00000199635	CpG island
IFNA7	CpG island
IFNA21	CpG island
IFNWP15	CpG island
IFNWP9	CpG island
IFNA14	CpG island
IFNA17	CpG island
IFNWP18	CpG island
IFNA16	CpG island
IFNA4	CpG island
IFNA10	CpG island
IFNWP5	CpG island

Extended variants
information (count: 1559 )
Associated
traits (count: 156 )

Variant overlapped rSNPs/rCNVs (count:1559 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10757193	chr9:21157373-21157374	Weak transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs556271942	chr9:21157395-21157396	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs576197112	chr9:21157397-21157398	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs143657828	chr9:21157428-21157429	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs112495057	chr9:21157439-21157440	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs191947331	chr9:21157479-21157480	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs76748120	chr9:21157506-21157507	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs182557111	chr9:21157530-21157531	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs185799964	chr9:21157541-21157542	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs561006823	chr9:21157551-21157552	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs190608211	chr9:21157559-21157560	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs141831374	chr9:21157575-21157576	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs549704730	chr9:21157602-21157603	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs10283629	chr9:21157695-21157696	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs565865553	chr9:21157716-21157717	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs532427438	chr9:21157739-21157740	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs552155415	chr9:21157749-21157750	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs148106416	chr9:21157761-21157762	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs376387412	chr9:21157814-21157815	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs370064264	chr9:21157815-21157816	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs559462962	chr9:21157832-21157833	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs529832258	chr9:21157849-21157850	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs568657960	chr9:21157881-21157882	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs372729757	chr9:21157905-21157906	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs557235044	chr9:21157916-21157917	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs576211069	chr9:21157939-21157940	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs375627354	chr9:21157945-21157946	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs142870670	chr9:21157947-21157948	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs558603909	chr9:21157951-21157952	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs182430272	chr9:21157953-21157954	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs114301602	chr9:21157984-21157985	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs12555190	chr9:21157997-21157998	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs187047280	chr9:21158006-21158007	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs190848793	chr9:21158012-21158013	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs543610642	chr9:21158038-21158039	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs146099583	chr9:21158044-21158045	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs532491912	chr9:21158054-21158055	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs552218733	chr9:21158057-21158058	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs140127290	chr9:21158059-21158060	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs182567954	chr9:21158095-21158096	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs13295726	chr9:21158124-21158125	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs548282834	chr9:21158125-21158126	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs552112225	chr9:21158169-21158170	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs188032223	chr9:21158176-21158177	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs538950354	chr9:21158183-21158184	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs115238465	chr9:21158210-21158211	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs118164246	chr9:21158223-21158224	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs7874284	chr9:21158252-21158253	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs540026200	chr9:21158261-21158262	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs150893818	chr9:21158270-21158271	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:156)

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
Breast cancer	21364760	CNVD
Adenoid cystic carcinoma	18332873	CNVD
Cancer	20581869	CNVD
XY gonadal dysgenesis	20685758	CNVD
Non-small cell lung cancer	16651412	CNVD
Multiple myeloma	17550852	CNVD
Intellectual disability	22102821	CNVD
Oral cancer	22144094	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Lung cancer	21569311	CNVD
Non-syndromic sensorineural hearing loss	19212409	CNVD
Epilepsy	20502679	CNVD
Barrett''s syndrome	19417022	CNVD

Chromatin state (count:98 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:21154600-21158800	Weak transcription	Monocytes-CD14+_RO01746	blood
2	chr9:21154600-21159400	Weak transcription	Primary neutrophils fromperipheralblood	blood
3	chr9:21154600-21160000	Weak transcription	Primary monocytes fromperipheralblood	blood
4	chr9:21154600-21160000	Weak transcription	GM12878-XiMat	blood
5	chr9:21154600-21160200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
6	chr9:21156800-21157400	ZNF genes & repeats	Dnd41	blood
7	chr9:21157400-21160000	Weak transcription	Dnd41	blood
8	chr9:21158800-21160000	Enhancers	Monocytes-CD14+_RO01746	blood
9	chr9:21158800-21161400	Enhancers	Primary T helper cells PMA-I stimulated	--
10	chr9:21159000-21159200	Enhancers	Primary T helper cells fromperipheralblood	blood
11	chr9:21159000-21161400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
12	chr9:21159000-21161600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
13	chr9:21159000-21161600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
14	chr9:21159200-21159800	Weak transcription	Primary T helper cells fromperipheralblood	blood
15	chr9:21159200-21161200	Enhancers	Primary T killer memory cells from peripheral blood	blood
16	chr9:21159400-21160600	Enhancers	Primary neutrophils fromperipheralblood	blood
17	chr9:21159400-21161400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
18	chr9:21159800-21161400	Enhancers	Primary T helper cells fromperipheralblood	blood
19	chr9:21160000-21160200	Enhancers	Primary T helper naive cells from peripheral blood	blood
20	chr9:21160000-21160400	Flanking Active TSS	GM12878-XiMat	blood
21	chr9:21160000-21160400	Enhancers	HMEC	breast
22	chr9:21160000-21160400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
23	chr9:21160000-21160600	Enhancers	Primary T regulatory cells fromperipheralblood	blood
24	chr9:21160000-21160600	Enhancers	HUVEC	blood vessel
25	chr9:21160000-21161000	Enhancers	Primary T cells from cord blood	blood
26	chr9:21160000-21161200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
27	chr9:21160000-21161400	Enhancers	Primary monocytes fromperipheralblood	blood
28	chr9:21160000-21161400	Enhancers	Dnd41	blood
29	chr9:21160200-21160400	Enhancers	Primary hematopoietic stem cells short term culture	blood
30	chr9:21160200-21160600	Enhancers	Primary B cells from cord blood	blood
31	chr9:21160200-21160600	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
32	chr9:21160200-21160600	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
33	chr9:21160400-21161000	Enhancers	Monocytes-CD14+_RO01746	blood
34	chr9:21160600-21161400	Enhancers	Primary T helper naive cells from peripheral blood	blood
35	chr9:21161600-21162600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
36	chr9:21161600-21163200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
37	chr9:21162800-21163000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
38	chr9:21163000-21163400	Enhancers	Primary T cells fromperipheralblood	blood
39	chr9:21163200-21163400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
40	chr9:21163400-21163600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
41	chr9:21169200-21170000	Enhancers	Primary monocytes fromperipheralblood	blood
42	chr9:21174600-21175400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
43	chr9:21174600-21175800	Enhancers	Fetal Heart	heart
44	chr9:21176000-21176400	Weak transcription	Fetal Heart	heart
45	chr9:21177400-21177600	Enhancers	Fetal Heart	heart
46	chr9:21182800-21184000	Enhancers	Monocytes-CD14+_RO01746	blood
47	chr9:21183000-21183400	Enhancers	Primary neutrophils fromperipheralblood	blood
48	chr9:21183000-21183400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
49	chr9:21183200-21184000	Enhancers	Primary monocytes fromperipheralblood	blood
50	chr9:21183400-21184000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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