Variant report

Variant	nsv1035128
Chromosome Location	chr9:21196300-21269669
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	chr9:21268139-21268356	GM12878	blood:	n/a	n/a
2	BATF	chr9:21213980-21214258	GM12878	blood:	n/a	n/a
3	BATF	chr9:21214009-21214242	GM12878	blood:	n/a	n/a
4	BATF	chr9:21236050-21236328	GM12878	blood:	n/a	n/a
5	BCL11A	chr9:21236007-21236322	GM12878	blood:	n/a	chr9:21236181-21236190
6	BCL11A	chr9:21236105-21236278	GM12878	blood:	n/a	chr9:21236181-21236190
7	BCL11A	chr9:21213900-21214291	GM12878	blood:	n/a	chr9:21214111-21214120
8	BCL11A	chr9:21213999-21214266	GM12878	blood:	n/a	chr9:21214111-21214120
9	BHLHE40	chr9:21235842-21236001	GM12878	blood:	n/a	n/a
10	BRCA1	chr9:21235836-21236005	Hela-S3	cervix:	n/a	n/a
11	CEBPB	chr9:21213807-21213921	IMR90	lung:	n/a	n/a
12	CEBPB	chr9:21235830-21236091	Hela-S3	cervix:	n/a	n/a
13	CHD1	chr9:21268063-21268075	GM12878	blood:	n/a	n/a
14	CTCF	chr9:21252820-21252970	GM12873	blood:	n/a	n/a
15	CTCF	chr9:21211379-21211440	Pancreas_OC	pancreas:	n/a	n/a
16	CTCF	chr9:21265603-21265724	GM19238	blood:	n/a	chr9:21265686-21265695 chr9:21265686-21265699 chr9:21265688-21265698 chr9:21265683-21265701
17	CTCF	chr9:21235840-21235990	Caco-2	colon:	n/a	chr9:21235917-21235938
18	CTCF	chr9:21251300-21251450	GM12872	blood:	n/a	n/a
19	CTCF	chr9:21252860-21253010	A549	lung:	n/a	n/a
20	CTCF	chr9:21253053-21253274	HepG2	liver:	n/a	chr9:21253177-21253190 chr9:21253174-21253192 chr9:21253176-21253197
21	CTCF	chr9:21213760-21213910	HUVEC	blood vessel:	n/a	n/a
22	CTCF	chr9:21235792-21236129	MCF-7	breast:	n/a	chr9:21235917-21235938
23	CTCF	chr9:21253150-21253219	MCF-7	breast:	n/a	chr9:21253177-21253190 chr9:21253174-21253192 chr9:21253176-21253197
24	CTCF	chr9:21213753-21213946	Hela-S3	cervix:	n/a	n/a
25	CTCF	chr9:21251360-21251510	GM12871	blood:	n/a	n/a
26	CTCF	chr9:21235779-21236113	A549	lung:	n/a	chr9:21235917-21235938
27	CTCF	chr9:21213880-21214030	HCM	heart:	n/a	n/a
28	CTCF	chr9:21235840-21235990	Hela-S3	cervix:	n/a	chr9:21235917-21235938
29	CTCF	chr9:21213532-21213622	GM10266	blood:	n/a	n/a
30	CTCF	chr9:21235880-21236030	GM12865	blood:	n/a	chr9:21235917-21235938
31	CTCF	chr9:21213800-21213950	GM12801	blood:	n/a	n/a
32	CTCF	chr9:21213660-21213810	HAc	cerebellar:	n/a	n/a
33	CTCF	chr9:21235800-21236025	GM13977	blood:	n/a	chr9:21235917-21235938
34	CTCF	chr9:21213760-21213910	AG09309	skin:	n/a	n/a
35	CTCF	chr9:21235840-21235990	MCF-7	breast:	n/a	chr9:21235917-21235938
36	CTCF	chr9:21213716-21214012	HCT-116	colon:	n/a	n/a
37	CTCF	chr9:21253120-21253270	GM12868	blood:	n/a	chr9:21253177-21253190 chr9:21253174-21253192 chr9:21253176-21253197
38	CTCF	chr9:21236320-21236470	GM12865	blood:	n/a	n/a
39	CTCF	chr9:21252997-21253346	A549	lung:	n/a	chr9:21253177-21253190 chr9:21253174-21253192 chr9:21253176-21253197
40	CTCF	chr9:21213700-21213850	GM12864	blood:	n/a	n/a
41	CTCF	chr9:21235789-21236029	GM10266	blood:	n/a	chr9:21235917-21235938
42	CTCF	chr9:21256560-21256710	GM12868	blood:	n/a	n/a
43	CTCF	chr9:21253140-21253290	AG09319	gingival:	n/a	chr9:21253177-21253190 chr9:21253174-21253192 chr9:21253176-21253197
44	CTCF	chr9:21253080-21253230	BE2_C	brain:	n/a	chr9:21253177-21253190 chr9:21253174-21253192 chr9:21253176-21253197
45	CTCF	chr9:21253120-21253270	HMEC	breast:	n/a	chr9:21253177-21253190 chr9:21253174-21253192 chr9:21253176-21253197
46	CTCF	chr9:21241820-21241970	GM06990	blood:	n/a	n/a
47	CTCF	chr9:21235840-21235990	GM12867	blood:	n/a	chr9:21235917-21235938
48	CTCF	chr9:21253100-21253250	HEEpiC	esophagus:	n/a	chr9:21253177-21253190 chr9:21253174-21253192 chr9:21253176-21253197
49	CTCF	chr9:21213680-21213830	HVMF	connective:	n/a	n/a
50	CTCF	chr9:21235797-21236108	MCF-7	breast:	n/a	chr9:21235917-21235938

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:21239944-21239994	NHDF-neo	bronchial:	n/a
2	chr9:21239944-21239994	HepG2	liver:	n/a
3	chr9:21239944-21239994	NHDF-neo	bronchial:	n/a
4	chr9:21239944-21239994	HepG2	liver:	n/a
5	chr9:21202213-21202263	IMR90	lung:	fetal
6	chr9:21202213-21202263	PANC-1	pancreas:	n/a
7	chr9:21239944-21239994	HCPEpiC	choroid plexus:	n/a
8	chr9:21241233-21241283	HRCEpiC	kidney:	n/a
9	chr9:21241233-21241283	HepG2	liver:	n/a
10	chr9:21239944-21239994	ovcar-3	ovarian:	n/a
11	chr9:21239944-21239994	HCT-116	colon:	n/a
12	chr9:21241233-21241283	HL-60	blood:	n/a
13	chr9:21239944-21239994	HL-60	blood:	n/a
14	chr9:21202213-21202263	NH-A	brain:	n/a
15	chr9:21202213-21202263	HCF	heart:	n/a
16	chr9:21241233-21241283	NHBE	bronchial:	n/a
17	chr9:21202213-21202263	SK-N-SH	brain:	n/a
18	chr9:21241233-21241283	A549	lung:	n/a
19	chr9:21239944-21239994	Caco-2	colon:	n/a
20	chr9:21202213-21202263	NHDF-neo	bronchial:	n/a
21	chr9:21239944-21239994	A549	lung:	n/a
22	chr9:21239944-21239994	K562	blood:	n/a
23	chr9:21202213-21202263	PFSK-1	brain:	n/a
24	chr9:21202213-21202263	HIPEpiC	eye:	n/a
25	chr9:21239944-21239994	ProgFib	skin:	n/a
26	chr9:21202213-21202263	LNCaP	prostate:	n/a
27	chr9:21202213-21202263	GM12878	blood:	n/a
28	chr9:21239944-21239994	RPTEC	kidney:	n/a
29	chr9:21241233-21241283	AG10803	skin:	n/a
30	chr9:21202213-21202263	HRE	kidney:	n/a
31	chr9:21241233-21241283	RPTEC	kidney:	n/a
32	chr9:21239944-21239994	PFSK-1	brain:	n/a
33	chr9:21202213-21202263	CMK	blood:	n/a
34	chr9:21202213-21202263	BJ	skin:	n/a
35	chr9:21202213-21202263	GM12891	blood:	n/a
36	chr9:21241233-21241283	AoSMC	blood vessel:	n/a
37	chr9:21241233-21241283	SAEC	small airway:	n/a
38	chr9:21202213-21202263	NHBE	bronchial:	n/a
39	chr9:21241233-21241283	U87	brain:	n/a
40	chr9:21239944-21239994	CMK	blood:	n/a
41	chr9:21239944-21239994	HRCEpiC	kidney:	n/a
42	chr9:21241233-21241283	AG09319	gingival:	n/a
43	chr9:21241233-21241283	T-47D	breast:	n/a
44	chr9:21239944-21239994	HCF	heart:	n/a
45	chr9:21241233-21241283	GM12892	blood:	n/a
46	chr9:21202213-21202263	HAEpiC	amniotic membrane:	n/a
47	chr9:21241233-21241283	HUVEC	blood vessel:	n/a
48	chr9:21239944-21239994	NT2-D1	testis:	n/a
49	chr9:21241233-21241283	HRE	kidney:	n/a
50	chr9:21202213-21202263	MCF-7	breast:	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr9:21253305..21254010-chr9:21318409..21318973,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-IFNA10-1	chr9:21209188-21209778	NONHSAT130374
2	lnc-IFNA17-1	chr9:21231265-21231852	NONHSAT130375

Variant related genes	Relation type
IFNA7	TF binding region
IFNA14	TF binding region
IFNA17	TF binding region
IFNWP18	TF binding region
IFNA16	TF binding region
IFNA10	TF binding region
IFNWP5	TF binding region
IFNA7	CpG island
IFNA14	CpG island
IFNA17	CpG island
IFNWP18	CpG island
IFNA16	CpG island
IFNA10	CpG island
IFNWP5	CpG island

Extended variants
information (count: 1484 )
Associated
traits (count: 155 )

Variant overlapped rSNPs/rCNVs (count:1484 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs5896928	chr9:21196333-21196334	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs527712745	chr9:21196334-21196335	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs547796232	chr9:21196336-21196337	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs397735579	chr9:21196344-21196345	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs372759709	chr9:21196345-21196346	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs2007448	chr9:21196356-21196357	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
7	rs117054388	chr9:21196375-21196376	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs573257661	chr9:21196398-21196399	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs542526543	chr9:21196401-21196402	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs528759441	chr9:21196406-21196407	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs556014059	chr9:21196432-21196433	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs575912788	chr9:21196433-21196434	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs181136891	chr9:21196434-21196435	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs186374059	chr9:21196464-21196465	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs143006883	chr9:21196469-21196470	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs541121657	chr9:21196474-21196475	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs7856345	chr9:21196490-21196491	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
18	rs529483522	chr9:21196497-21196498	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs190858915	chr9:21196503-21196504	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs550177195	chr9:21196512-21196513	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs7870352	chr9:21196515-21196516	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs532685034	chr9:21196523-21196524	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs552783669	chr9:21196537-21196538	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs566091991	chr9:21196539-21196540	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs533894974	chr9:21196562-21196563	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs368182744	chr9:21196580-21196581	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs553415265	chr9:21196605-21196606	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs566947794	chr9:21196624-21196625	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs535874934	chr9:21196671-21196672	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs7043362	chr9:21196710-21196711	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs569696274	chr9:21196775-21196776	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs571004357	chr9:21196794-21196795	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs375063992	chr9:21196830-21196831	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs369202181	chr9:21196836-21196837	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs371316641	chr9:21196840-21196841	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs3855766	chr9:21196842-21196843	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
37	rs13292080	chr9:21196851-21196852	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs558720912	chr9:21196855-21196856	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs4007648	chr9:21196902-21196903	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs374272105	chr9:21196903-21196904	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs10124609	chr9:21196907-21196908	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
42	rs534637114	chr9:21196909-21196910	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs573787714	chr9:21196912-21196913	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs4007649	chr9:21196929-21196930	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs4007650	chr9:21196932-21196933	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs568211528	chr9:21196950-21196951	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs543877456	chr9:21196959-21196960	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs559597128	chr9:21196962-21196963	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs7870692	chr9:21196978-21196979	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs532841166	chr9:21196982-21196983	Weak transcription 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
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
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:200 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:21195600-21196400	Enhancers	Primary monocytes fromperipheralblood	blood
2	chr9:21196200-21196600	Weak transcription	GM12878-XiMat	blood
3	chr9:21196400-21197600	Weak transcription	Primary monocytes fromperipheralblood	blood
4	chr9:21196600-21197000	Enhancers	GM12878-XiMat	blood
5	chr9:21198000-21198200	Enhancers	Primary monocytes fromperipheralblood	blood
6	chr9:21198200-21198800	Enhancers	Placenta	Placenta
7	chr9:21211400-21211800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr9:21211400-21212200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr9:21228000-21228400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr9:21236000-21236200	Enhancers	Primary hematopoietic stem cells	blood
11	chr9:21236000-21236200	Enhancers	Primary T helper cells fromperipheralblood	blood
12	chr9:21236000-21236200	Bivalent Enhancer	Dnd41	blood
13	chr9:21236000-21236200	Active TSS	Hela-S3	cervix
14	chr9:21236000-21236200	Enhancers	Monocytes-CD14+_RO01746	blood
15	chr9:21236000-21236400	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr9:21236000-21236400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
17	chr9:21236000-21236400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
18	chr9:21236000-21236400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
19	chr9:21236000-21236600	Enhancers	Primary T helper cells PMA-I stimulated	--
20	chr9:21236000-21236600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
21	chr9:21236000-21236600	Enhancers	Primary T killer memory cells from peripheral blood	blood
22	chr9:21236000-21236800	Enhancers	Primary T cells from cord blood	blood
23	chr9:21236200-21236400	Flanking Active TSS	Hela-S3	cervix
24	chr9:21236200-21236600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
25	chr9:21236200-21236600	Enhancers	Primary T helper naive cells from peripheral blood	blood
26	chr9:21236200-21244600	Weak transcription	Primary hematopoietic stem cells	blood
27	chr9:21236400-21239800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
28	chr9:21236400-21244600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
29	chr9:21239400-21239600	Enhancers	Monocytes-CD14+_RO01746	blood
30	chr9:21239400-21240800	Enhancers	Primary monocytes fromperipheralblood	blood
31	chr9:21239600-21240200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
32	chr9:21239600-21240600	Enhancers	Primary neutrophils fromperipheralblood	blood
33	chr9:21239800-21240000	Bivalent Enhancer	Esophagus	oesophagus
34	chr9:21239800-21240000	Enhancers	Lung	lung
35	chr9:21239800-21240200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
36	chr9:21239800-21240400	Enhancers	GM12878-XiMat	blood
37	chr9:21240200-21240800	Enhancers	Monocytes-CD14+_RO01746	blood
38	chr9:21240200-21244600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
39	chr9:21240400-21245000	Weak transcription	GM12878-XiMat	blood
40	chr9:21240600-21245000	Weak transcription	Primary neutrophils fromperipheralblood	blood
41	chr9:21243200-21243600	Enhancers	Hela-S3	cervix
42	chr9:21244600-21245400	Enhancers	Primary hematopoietic stem cells	blood
43	chr9:21244600-21245400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
44	chr9:21244600-21245600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
45	chr9:21244600-21245800	Enhancers	Primary hematopoietic stem cells short term culture	blood
46	chr9:21244600-21245800	Enhancers	Monocytes-CD14+_RO01746	blood
47	chr9:21244600-21246000	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood
48	chr9:21245000-21245200	Enhancers	GM12878-XiMat	blood
49	chr9:21245000-21245400	Enhancers	Primary neutrophils fromperipheralblood	blood
50	chr9:21245400-21246000	Weak transcription	Primary neutrophils fromperipheralblood	blood

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