Variant report

Variant	nsv1016978
Chromosome Location	chr9:21171267-21214877
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	chr9:21183393-21183622	GM12878	blood:	n/a	n/a
2	BATF	chr9:21195481-21195714	GM12878	blood:	n/a	n/a
3	BATF	chr9:21213980-21214258	GM12878	blood:	n/a	n/a
4	BATF	chr9:21214009-21214242	GM12878	blood:	n/a	n/a
5	BATF	chr9:21195452-21195727	GM12878	blood:	n/a	n/a
6	BATF	chr9:21183391-21183669	GM12878	blood:	n/a	n/a
7	BCL11A	chr9:21183431-21183637	GM12878	blood:	n/a	chr9:21183522-21183531
8	BCL11A	chr9:21213999-21214266	GM12878	blood:	n/a	chr9:21214111-21214120
9	BCL11A	chr9:21213900-21214291	GM12878	blood:	n/a	chr9:21214111-21214120
10	BCL11A	chr9:21195471-21195683	GM12878	blood:	n/a	chr9:21195583-21195592
11	BCL11A	chr9:21195389-21195749	GM12878	blood:	n/a	chr9:21195583-21195592
12	BHLHE40	chr9:21195256-21195293	GM12878	blood:	n/a	n/a
13	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
14	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
15	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
16	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
17	CEBPB	chr9:21183206-21183372	A549	lung:	n/a	n/a
18	CEBPB	chr9:21213807-21213921	IMR90	lung:	n/a	n/a
19	CEBPB	chr9:21172238-21172445	HepG2	liver:	n/a	chr9:21172346-21172357
20	CEBPB	chr9:21172249-21172496	A549	lung:	n/a	chr9:21172346-21172357
21	CTCF	chr9:21183080-21183230	RPTEC	kidney:	n/a	n/a
22	CTCF	chr9:21213700-21213850	GM12868	blood:	n/a	n/a
23	CTCF	chr9:21195240-21195390	SAEC	small airway:	n/a	chr9:21195318-21195336
24	CTCF	chr9:21195203-21195373	MCF-7	breast:	n/a	chr9:21195318-21195336
25	CTCF	chr9:21183536-21183600	GM10266	blood:	n/a	n/a
26	CTCF	chr9:21195148-21195378	A549	lung:	n/a	chr9:21195318-21195336
27	CTCF	chr9:21183200-21183350	GM12875	blood:	n/a	chr9:21183259-21183277
28	CTCF	chr9:21213680-21213830	NHLF	lung:	n/a	n/a
29	CTCF	chr9:21213739-21213950	HepG2	liver:	n/a	n/a
30	CTCF	chr9:21195140-21195290	RPTEC	kidney:	n/a	n/a
31	CTCF	chr9:21183100-21183250	GM12872	blood:	n/a	n/a
32	CTCF	chr9:21195120-21195270	HVMF	connective:	n/a	n/a
33	CTCF	chr9:21195260-21195410	GM12867	blood:	n/a	chr9:21195318-21195336
34	CTCF	chr9:21213760-21213910	GM12874	blood:	n/a	n/a
35	CTCF	chr9:21183080-21183230	GM12866	blood:	n/a	n/a
36	CTCF	chr9:21183300-21183450	HAc	cerebellar:	n/a	n/a
37	CTCF	chr9:21183060-21183210	HVMF	connective:	n/a	n/a
38	CTCF	chr9:21195224-21195405	SK-N-SH_RA	brain:	n/a	chr9:21195318-21195336
39	CTCF	chr9:21213686-21213962	SK-N-SH_RA	brain:	n/a	n/a
40	CTCF	chr9:21195179-21195510	HUVEC	blood vessel:	n/a	chr9:21195318-21195336
41	CTCF	chr9:21183280-21183430	HFF	foreskin:	n/a	n/a
42	CTCF	chr9:21213780-21213930	HMEC	breast:	n/a	n/a
43	CTCF	chr9:21195140-21195290	NHDF-neo	bronchial:	n/a	n/a
44	CTCF	chr9:21213780-21213930	HEEpiC	esophagus:	n/a	n/a
45	CTCF	chr9:21213760-21213910	HUVEC	blood vessel:	n/a	n/a
46	CTCF	chr9:21213760-21213910	HMF	breast:	n/a	n/a
47	CTCF	chr9:21205784-21205810	Medullo	brain:	n/a	n/a
48	CTCF	chr9:21213740-21213890	GM12865	blood:	n/a	n/a
49	CTCF	chr9:21213787-21213913	H1-hESC	embryonic stem cell:	n/a	n/a
50	CTCF	chr9:21195222-21195424	HepG2	liver:	n/a	chr9:21195318-21195336

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:21202213-21202263	H1-hESC	embryonic stem cell:	embryo
2	chr9:21187344-21187394	HEK293	kidney:	embryo
3	chr9:21187344-21187394	HNPCEpiC	eye:	n/a
4	chr9:21202213-21202263	AG09319	gingival:	n/a
5	chr9:21202213-21202263	MCF-7	breast:	n/a
6	chr9:21202213-21202263	ProgFib	skin:	n/a
7	chr9:21202213-21202263	IMR90	lung:	fetal
8	chr9:21202213-21202263	SK-N-SH	brain:	n/a
9	chr9:21187344-21187394	GM19239	blood:	n/a
10	chr9:21202213-21202263	AG10803	skin:	n/a
11	chr9:21202213-21202263	GM12892	blood:	n/a
12	chr9:21187344-21187394	NT2-D1	testis:	n/a
13	chr9:21187344-21187394	HPAEpiC	pulmonary alveolar:	n/a
14	chr9:21202213-21202263	A549	lung:	n/a
15	chr9:21187344-21187394	GM06990	blood:	n/a
16	chr9:21202213-21202263	HCM	heart:	n/a
17	chr9:21187344-21187394	HRE	kidney:	n/a
18	chr9:21202213-21202263	NHBE	bronchial:	n/a
19	chr9:21202213-21202263	GM06990	blood:	n/a
20	chr9:21187344-21187394	SAEC	small airway:	n/a
21	chr9:21187344-21187394	AG04449	skin:	fetal
22	chr9:21187344-21187394	HIPEpiC	eye:	n/a
23	chr9:21187344-21187394	ProgFib	skin:	n/a
24	chr9:21202213-21202263	ovcar-3	ovarian:	n/a
25	chr9:21202213-21202263	PANC-1	pancreas:	n/a
26	chr9:21187344-21187394	LNCaP	prostate:	n/a
27	chr9:21202213-21202263	AG09309	skin:	n/a
28	chr9:21202213-21202263	Jurkat	blood:	n/a
29	chr9:21187344-21187394	NH-A	brain:	n/a
30	chr9:21187344-21187394	SK-N-MC	brain:	n/a
31	chr9:21202213-21202263	GM12891	blood:	n/a
32	chr9:21187344-21187394	SKMC	muscle:	n/a
33	chr9:21187344-21187394	Hela-S3	cervix:	n/a
34	chr9:21202213-21202263	HCPEpiC	choroid plexus:	n/a
35	chr9:21187344-21187394	AG09309	skin:	n/a
36	chr9:21187344-21187394	HepG2	liver:	n/a
37	chr9:21187344-21187394	RPTEC	kidney:	n/a
38	chr9:21187344-21187394	PFSK-1	brain:	n/a
39	chr9:21202213-21202263	AG04449	skin:	fetal
40	chr9:21187344-21187394	HCT-116	colon:	n/a
41	chr9:21187344-21187394	HRCEpiC	kidney:	n/a
42	chr9:21187344-21187394	A549	lung:	n/a
43	chr9:21187344-21187394	GM12892	blood:	n/a
44	chr9:21202213-21202263	RPTEC	kidney:	n/a
45	chr9:21187344-21187394	GM12878	blood:	n/a
46	chr9:21187344-21187394	HCPEpiC	choroid plexus:	n/a
47	chr9:21202213-21202263	LNCaP	prostate:	n/a
48	chr9:21202213-21202263	Hepatocyte	liver:	n/a
49	chr9:21187344-21187394	ECC-1	luminal epithelium:	n/a
50	chr9:21187344-21187394	NHBE	bronchial:	n/a

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

Variant related genes	Relation type
IFNA7	TF binding region
IFNA21	TF binding region
IFNWP15	TF binding region
IFNA10	TF binding region
IFNWP9	TF binding region
IFNWP18	TF binding region
IFNA4	TF binding region
IFNA7	CpG island
IFNA21	CpG island
IFNWP15	CpG island
IFNA10	CpG island
IFNWP9	CpG island
IFNWP18	CpG island
IFNA4	CpG island

Extended variants
information (count: 656 )
Associated
traits (count: 155 )

Variant overlapped rSNPs/rCNVs (count:656 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10964878	chr9:21171267-21171268	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs7852323	chr9:21174643-21174644	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs551700040	chr9:21174645-21174646	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs559790716	chr9:21174649-21174650	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs79880106	chr9:21174652-21174653	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs534130545	chr9:21174655-21174656	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs561158494	chr9:21174662-21174663	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs553911979	chr9:21174664-21174665	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs182000346	chr9:21174699-21174700	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs535224230	chr9:21174702-21174703	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs371389329	chr9:21174711-21174712	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs117663850	chr9:21174726-21174727	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs200239481	chr9:21174731-21174732	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs7852685	chr9:21174745-21174746	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs528428254	chr9:21174811-21174812	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs140759620	chr9:21174818-21174819	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs144606932	chr9:21174842-21174843	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs7024604	chr9:21174878-21174879	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs138570454	chr9:21174892-21174893	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs185797647	chr9:21174939-21174940	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs529064033	chr9:21174961-21174962	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs190092217	chr9:21174962-21174963	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs370764210	chr9:21174966-21174967	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs181170060	chr9:21175048-21175049	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs369599747	chr9:21175090-21175091	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs531608302	chr9:21175094-21175095	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs186401524	chr9:21175108-21175109	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs571620365	chr9:21175119-21175120	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs80236572	chr9:21175185-21175186	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs115208877	chr9:21175192-21175193	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs190870450	chr9:21175193-21175194	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs182584112	chr9:21175212-21175213	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs548814213	chr9:21175243-21175244	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs200044449	chr9:21175257-21175258	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs201768891	chr9:21175264-21175265	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs373133087	chr9:21175265-21175266	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs200316657	chr9:21175266-21175267	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs568887560	chr9:21175280-21175281	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs537861850	chr9:21175291-21175292	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs377757546	chr9:21175308-21175309	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs116745560	chr9:21175372-21175373	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs577697211	chr9:21175393-21175394	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs143517852	chr9:21175415-21175416	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs80252344	chr9:21175450-21175451	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs185496267	chr9:21175459-21175460	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs148029019	chr9:21175483-21175484	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs565768259	chr9:21175497-21175498	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs141759893	chr9:21175504-21175505	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs980639	chr9:21175516-21175517	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
50	rs576102535	chr9:21175524-21175525	Enhancers	n/a	n/a	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
Breast cancer	21364760	CNVD
Adenoid cystic carcinoma	18332873	CNVD
Cancer	20581869	CNVD
XY gonadal dysgenesis	20685758	CNVD
Multiple myeloma	17550852	CNVD
Intellectual disability	22102821	CNVD
Oral cancer	22144094	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD
Lung cancer	21569311	CNVD
Non-syndromic sensorineural hearing loss	19212409	CNVD
Epilepsy	20502679	CNVD
Barrett''s syndrome	19417022	CNVD

Chromatin state (count:25 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:21174600-21175400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
2	chr9:21174600-21175800	Enhancers	Fetal Heart	heart
3	chr9:21176000-21176400	Weak transcription	Fetal Heart	heart
4	chr9:21177400-21177600	Enhancers	Fetal Heart	heart
5	chr9:21182800-21184000	Enhancers	Monocytes-CD14+_RO01746	blood
6	chr9:21183000-21183400	Enhancers	Primary neutrophils fromperipheralblood	blood
7	chr9:21183000-21183400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
8	chr9:21183200-21184000	Enhancers	Primary monocytes fromperipheralblood	blood
9	chr9:21183400-21184000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chr9:21195200-21195600	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr9:21195200-21195800	Active TSS	Hela-S3	cervix
12	chr9:21195200-21196000	Enhancers	Primary neutrophils fromperipheralblood	blood
13	chr9:21195200-21196000	Enhancers	Monocytes-CD14+_RO01746	blood
14	chr9:21195400-21195800	Enhancers	Primary hematopoietic stem cells	blood
15	chr9:21195600-21195800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr9:21195600-21196200	Enhancers	GM12878-XiMat	blood
17	chr9:21195600-21196400	Enhancers	Primary monocytes fromperipheralblood	blood
18	chr9:21195800-21196000	Enhancers	Hela-S3	cervix
19	chr9:21196200-21196600	Weak transcription	GM12878-XiMat	blood
20	chr9:21196400-21197600	Weak transcription	Primary monocytes fromperipheralblood	blood
21	chr9:21196600-21197000	Enhancers	GM12878-XiMat	blood
22	chr9:21198000-21198200	Enhancers	Primary monocytes fromperipheralblood	blood
23	chr9:21198200-21198800	Enhancers	Placenta	Placenta
24	chr9:21211400-21211800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
25	chr9:21211400-21212200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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