Variant report

Variant	nsv893767
Chromosome Location	chr9:117627569-117689838
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1376)
CpG islands
(count:122)
Chromatin interactive
region (count:40)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1376 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:117650412-117650644	HepG2	liver:	n/a	n/a
2	ARID3A	chr9:117647074-117647431	HepG2	liver:	n/a	n/a
3	ARID3A	chr9:117670365-117670753	HepG2	liver:	n/a	n/a
4	ATF3	chr9:117670162-117670885	A549	lung:	n/a	n/a
5	ATF3	chr9:117670180-117670875	A549	lung:	n/a	n/a
6	ATF3	chr9:117646923-117647482	A549	lung:	n/a	n/a
7	BATF	chr9:117657122-117657454	GM12878	blood:	n/a	n/a
8	BATF	chr9:117646054-117646236	GM12878	blood:	n/a	n/a
9	BCL3	chr9:117670204-117670998	A549	lung:	n/a	n/a
10	BCL3	chr9:117646931-117647489	A549	lung:	n/a	n/a
11	BCL3	chr9:117670143-117670942	A549	lung:	n/a	n/a
12	BCL3	chr9:117646964-117647566	A549	lung:	n/a	n/a
13	BHLHE40	chr9:117647131-117647472	HepG2	liver:	n/a	n/a
14	BRCA1	chr9:117669340-117669575	Hela-S3	cervix:	n/a	n/a
15	BRCA1	chr9:117657092-117657569	Hela-S3	cervix:	n/a	n/a
16	BRCA1	chr9:117670248-117670950	Hela-S3	cervix:	n/a	n/a
17	CBX3	chr9:117670347-117670878	HCT-116	colon:	n/a	n/a
18	CEBPB	chr9:117650988-117651130	H1-hESC	embryonic stem cell:	n/a	n/a
19	CEBPB	chr9:117646996-117647518	A549	lung:	n/a	n/a
20	CEBPB	chr9:117670214-117670931	MCF-7	breast:	n/a	n/a
21	CEBPB	chr9:117658021-117658371	IMR90	lung:	n/a	chr9:117658196-117658207
22	CEBPB	chr9:117646085-117646216	IMR90	lung:	n/a	n/a
23	CEBPB	chr9:117658036-117658363	Hela-S3	cervix:	n/a	chr9:117658196-117658207
24	CEBPB	chr9:117663331-117664039	IMR90	lung:	n/a	n/a
25	CEBPB	chr9:117657172-117657502	HepG2	liver:	n/a	chr9:117657346-117657357
26	CEBPB	chr9:117646069-117646321	A549	lung:	n/a	n/a
27	CEBPB	chr9:117647079-117647476	Hela-S3	cervix:	n/a	n/a
28	CEBPB	chr9:117656507-117656746	A549	lung:	n/a	n/a
29	CEBPB	chr9:117657007-117657639	A549	lung:	n/a	chr9:117657346-117657357
30	CEBPB	chr9:117657941-117658337	HepG2	liver:	n/a	chr9:117658196-117658207
31	CEBPB	chr9:117642647-117642854	IMR90	lung:	n/a	n/a
32	CEBPB	chr9:117656480-117657600	IMR90	lung:	n/a	chr9:117657346-117657357
33	CEBPB	chr9:117647165-117647386	K562	blood:	n/a	n/a
34	CEBPB	chr9:117647100-117647502	HepG2	liver:	n/a	n/a
35	CEBPB	chr9:117670205-117671004	MCF-7	breast:	n/a	n/a
36	CEBPB	chr9:117650299-117650625	HepG2	liver:	n/a	chr9:117650474-117650485
37	CEBPB	chr9:117658678-117658946	K562	blood:	n/a	chr9:117658828-117658839
38	CEBPB	chr9:117672448-117672772	HepG2	liver:	n/a	chr9:117672602-117672613
39	CEBPB	chr9:117650329-117650593	A549	lung:	n/a	chr9:117650474-117650485
40	CEBPB	chr9:117670319-117670772	A549	lung:	n/a	n/a
41	CEBPB	chr9:117670136-117670979	A549	lung:	n/a	n/a
42	CEBPB	chr9:117670283-117670896	A549	lung:	n/a	n/a
43	CEBPB	chr9:117647030-117647442	HepG2	liver:	n/a	n/a
44	CEBPB	chr9:117672451-117672767	A549	lung:	n/a	chr9:117672602-117672613
45	CEBPB	chr9:117658677-117658984	IMR90	lung:	n/a	chr9:117658828-117658839
46	CEBPB	chr9:117672508-117672742	Hela-S3	cervix:	n/a	chr9:117672602-117672613
47	CEBPB	chr9:117672436-117672758	IMR90	lung:	n/a	chr9:117672602-117672613
48	CEBPB	chr9:117656451-117657619	Hela-S3	cervix:	n/a	chr9:117657346-117657357
49	CEBPB	chr9:117647057-117647418	MCF-7	breast:	n/a	n/a
50	CEBPB	chr9:117670274-117671654	Hela-S3	cervix:	n/a	chr9:117671573-117671586

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:117657237-117657287	HCPEpiC	choroid plexus:	n/a
2	chr9:117657237-117657287	U87	brain:	n/a
3	chr9:117657237-117657287	ECC-1	luminal epithelium:	n/a
4	chr9:117657237-117657287	PFSK-1	brain:	n/a
5	chr9:117673469-117673519	Jurkat	blood:	n/a
6	chr9:117673469-117673519	GM19239	blood:	n/a
7	chr9:117673469-117673519	T-47D	breast:	n/a
8	chr9:117657237-117657287	HCT-116	colon:	n/a
9	chr9:117673469-117673519	HRE	kidney:	n/a
10	chr9:117673469-117673519	HMEC	breast:	n/a
11	chr9:117657237-117657287	HRE	kidney:	n/a
12	chr9:117657237-117657287	PANC-1	pancreas:	n/a
13	chr9:117673469-117673519	NHDF-neo	bronchial:	n/a
14	chr9:117657237-117657287	HMEC	breast:	n/a
15	chr9:117673469-117673519	SK-N-SH	brain:	n/a
16	chr9:117657237-117657287	AG04450	lung:	fetal
17	chr9:117657237-117657287	BJ	skin:	n/a
18	chr9:117657237-117657287	PrEC	prostate:	n/a
19	chr9:117673469-117673519	NHBE	bronchial:	n/a
20	chr9:117673469-117673519	AG04449	skin:	fetal
21	chr9:117673469-117673519	U87	brain:	n/a
22	chr9:117657237-117657287	GM19239	blood:	n/a
23	chr9:117657237-117657287	HEK293	kidney:	embryo
24	chr9:117657237-117657287	Hela-S3	cervix:	n/a
25	chr9:117673469-117673519	Caco-2	colon:	n/a
26	chr9:117673469-117673519	ProgFib	skin:	n/a
27	chr9:117673469-117673519	AG09319	gingival:	n/a
28	chr9:117657237-117657287	HNPCEpiC	eye:	n/a
29	chr9:117673469-117673519	ovcar-3	ovarian:	n/a
30	chr9:117657237-117657287	ovcar-3	ovarian:	n/a
31	chr9:117673469-117673519	HEK293	kidney:	embryo
32	chr9:117673469-117673519	HRPEpiC	eye:	n/a
33	chr9:117673469-117673519	Hepatocyte	liver:	n/a
34	chr9:117657237-117657287	SAEC	small airway:	n/a
35	chr9:117673469-117673519	SKMC	muscle:	n/a
36	chr9:117657237-117657287	CMK	blood:	n/a
37	chr9:117657237-117657287	NHBE	bronchial:	n/a
38	chr9:117657237-117657287	A549	lung:	n/a
39	chr9:117657237-117657287	GM12891	blood:	n/a
40	chr9:117657237-117657287	GM12878	blood:	n/a
41	chr9:117657237-117657287	HL-60	blood:	n/a
42	chr9:117673469-117673519	SAEC	small airway:	n/a
43	chr9:117657237-117657287	AG10803	skin:	n/a
44	chr9:117657237-117657287	SKMC	muscle:	n/a
45	chr9:117673469-117673519	AG09309	skin:	n/a
46	chr9:117657237-117657287	HUVEC	blood vessel:	n/a
47	chr9:117673469-117673519	ECC-1	luminal epithelium:	n/a
48	chr9:117657237-117657287	NHDF-neo	bronchial:	n/a
49	chr9:117657237-117657287	HepG2	liver:	n/a
50	chr9:117673469-117673519	HCF	heart:	n/a

(count:40 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:117685063..117687885-chr9:117689510..117691619,2	MCF-7	breast:
2	chr9:117652267..117654785-chr9:117659593..117661164,2	K562	blood:
3	chr9:117676278..117677112-chr9:117777453..117778259,2	MCF-7	breast:
4	chr9:117443850..117445001-chr9:117673133..117675031,14	MCF-7	breast:
5	chr9:117653018..117655628-chr9:117662655..117665359,2	MCF-7	breast:
6	chr9:117444446..117445144-chr9:117675660..117676526,3	MCF-7	breast:
7	chr9:117683235..117685068-chr9:117691767..117694448,2	MCF-7	breast:
8	chr9:117660259..117663236-chr9:117664218..117666178,2	MCF-7	breast:
9	chr9:117443662..117444548-chr9:117673210..117673712,2	MCF-7	breast:
10	chr7:81293610..81294606-chr9:117669034..117669870,2	MCF-7	breast:
11	chr9:117500707..117501777-chr9:117668813..117670087,8	MCF-7	breast:
12	chr9:117677998..117681403-chr9:117681907..117683952,3	MCF-7	breast:
13	chr9:117499604..117500209-chr9:117673251..117674135,2	MCF-7	breast:
14	chr9:117497188..117498694-chr9:117669038..117671472,2	MCF-7	breast:
15	chr9:117659568..117662536-chr9:117667322..117669249,2	K562	blood:
16	chr9:117685063..117687885-chr9:117689510..117691619,2	MCF-7	breast:
17	chr9:117672786..117673783-chr9:117775999..117776990,4	MCF-7	breast:
18	chr9:117423941..117424774-chr9:117672688..117673402,2	MCF-7	breast:
19	chr9:117500366..117501739-chr9:117668970..117671073,8	MCF-7	breast:
20	chr9:117503657..117504194-chr9:117669070..117669921,2	MCF-7	breast:
21	chr9:117660259..117663236-chr9:117664218..117666178,2	MCF-7	breast:
22	chr4:3387607..3388365-chr9:117671645..117672374,2	MCF-7	breast:
23	chr9:117444057..117444936-chr9:117676554..117677068,2	MCF-7	breast:
24	chr9:117442886..117445805-chr9:117668669..117671116,2	MCF-7	breast:
25	chr9:117500823..117501813-chr9:117672459..117674068,13	MCF-7	breast:
26	chr9:117677998..117681403-chr9:117681907..117683952,3	MCF-7	breast:
27	chr9:117652267..117654785-chr9:117659593..117661164,2	K562	blood:
28	chr1:121484470..121485223-chr9:117668926..117669480,2	MCF-7	breast:
29	chr9:117676108..117677078-chr9:117776037..117776911,10	MCF-7	breast:
30	chr9:117659568..117662536-chr9:117667322..117669249,2	K562	blood:
31	chr9:117443571..117445056-chr9:117668906..117670084,6	MCF-7	breast:
32	chr9:117660650..117663296-chr9:117774626..117776386,2	MCF-7	breast:
33	chr9:117653018..117655628-chr9:117662655..117665359,2	MCF-7	breast:
34	chr9:117424187..117425031-chr9:117672821..117673695,3	MCF-7	breast:
35	chr9:117676811..117678604-chr9:117693310..117696147,2	MCF-7	breast:
36	chr9:117501090..117501824-chr9:117669215..117669812,2	K562	blood:
37	chr9:117676223..117677155-chr9:117776236..117776995,3	MCF-7	breast:
38	chr9:117443784..117445753-chr9:117667939..117670651,2	MCF-7	breast:
39	chr9:117501292..117502939-chr9:117669201..117671782,2	MCF-7	breast:
40	chr9:117500881..117501577-chr9:117673361..117674100,4	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TNFSF8-1	chr9:117666507-117666588	NONHSAT134405
2	lnc-DEC1-7	chr9:117664203-117664893	NONHSAT134406
3	lnc-TNFSF8-1	chr9:117656003-117656444	NONHSAT134405

No data

Variant related genes	Relation type
TNFSF8	TF binding region
TNFSF8	CpG island
ENSG00000106952	chromatin interactions
ENSG00000230054	chromatin interactions
ENSG00000159788	chromatin interactions

Extended variants
information (count: 2257 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:2257 , 50 per page) page: 1 2 3 4 5 6 7 ... 46

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7866342	chr9:117627569-117627570	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs186999198	chr9:117627609-117627610	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs572814992	chr9:117627673-117627674	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs570805358	chr9:117627714-117627715	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs545108200	chr9:117627745-117627746	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs76042340	chr9:117627779-117627780	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs117578612	chr9:117627789-117627790	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs544557026	chr9:117627792-117627793	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs561126123	chr9:117627841-117627842	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs148815779	chr9:117627886-117627887	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs78222685	chr9:117627903-117627904	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs559813836	chr9:117627953-117627954	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs200753735	chr9:117627968-117627969	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs528615422	chr9:117627974-117627975	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs142577262	chr9:117627983-117627984	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs150952940	chr9:117627990-117627991	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs550863480	chr9:117627995-117627996	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs377504543	chr9:117628002-117628003	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs370678962	chr9:117628006-117628007	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs191823881	chr9:117628041-117628042	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs546311470	chr9:117628048-117628049	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs566440782	chr9:117628052-117628053	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs531072599	chr9:117628149-117628150	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs141792925	chr9:117628152-117628153	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs558677080	chr9:117628193-117628194	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs74687614	chr9:117628194-117628195	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs570611560	chr9:117628290-117628291	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs537992753	chr9:117628332-117628333	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs34474116	chr9:117628356-117628357	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs115612374	chr9:117628360-117628361	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs147087196	chr9:117628376-117628377	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs183674069	chr9:117628462-117628463	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs559519160	chr9:117628474-117628475	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs538103177	chr9:117628503-117628504	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs7043505	chr9:117628528-117628529	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs138441167	chr9:117628555-117628556	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs568373843	chr9:117628614-117628615	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs79764767	chr9:117628618-117628619	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs531028955	chr9:117628631-117628632	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs550726457	chr9:117628834-117628835	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs145053641	chr9:117628836-117628837	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs556958735	chr9:117628848-117628849	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs561515185	chr9:117628857-117628858	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs530354417	chr9:117628881-117628882	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs547267552	chr9:117628884-117628885	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs111473339	chr9:117628888-117628889	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs114788975	chr9:117628939-117628940	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs554199333	chr9:117628962-117628963	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs552305044	chr9:117629037-117629038	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs112825620	chr9:117629044-117629045	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:58)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
Renal cell carcinoma	18592004	CNVD
Developmental delay	19490664	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Medulloblastoma	21979893	CNVD
microdeletion syndrome	16199537	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Urothelial carcinoma	21177765	CNVD
Renal cell carcinoma	21668985	CNVD
Autism	22495311	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	16751803	CNVD
Myelofibrosis	22110671	CNVD
lymphocytic leukemia	21291569	CNVD
Leukemia	17361228	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Glioblastoma	16823260	CNVD
Non-small cell lung cancer	21044232	CNVD
Brain cancer	20823417	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Renal cell carcinoma	19461508	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Heart disease	21282601	CNVD
Lung cancer	18438408	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	17603634	CNVD
Acute myeloid leukemia	20729466	CNVD
Oral cancer	21386901	CNVD
Prostate cancer	18632612	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Gastric cancer	17908304	CNVD
small cell lung cancer	20016488	CNVD
Cardiac fibroma	18329553	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Testicular germ cell tumor	18059402	CNVD
Breast cancer	21364760	CNVD
Developmental delay	21147756	CNVD
Lung cancer	19147751	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Melanoma	18172304	CNVD
Colorectal cancer	16272173	CNVD
Bladder cancer	21909424	CNVD
Breast cancer	21509527	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Cervical cancer	16585170	CNVD
Ependymoma	19289631	CNVD

Chromatin state (count:1376 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:117626400-117627600	Enhancers	Muscle Satellite Cultured Cells	--
2	chr9:117626800-117627600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
3	chr9:117626800-117627600	Enhancers	HSMM	muscle
4	chr9:117626800-117628000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
5	chr9:117627000-117627600	Enhancers	NHEK	skin
6	chr9:117627400-117627600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
7	chr9:117627600-117632000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
8	chr9:117629200-117629400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
9	chr9:117629200-117629600	Enhancers	Primary T regulatory cells fromperipheralblood	blood
10	chr9:117629400-117630400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
11	chr9:117629600-117629800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
12	chr9:117629600-117631400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
13	chr9:117629800-117630800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
14	chr9:117630400-117632000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
15	chr9:117630600-117632200	Enhancers	Primary T helper cells PMA-I stimulated	--
16	chr9:117630800-117631800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
17	chr9:117630800-117632000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
18	chr9:117631000-117631600	Enhancers	Primary T helper naive cells from peripheral blood	blood
19	chr9:117631400-117631600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
20	chr9:117631400-117631600	Enhancers	Primary T killer memory cells from peripheral blood	blood
21	chr9:117631400-117632200	Enhancers	Primary T helper cells fromperipheralblood	blood
22	chr9:117631400-117632200	Enhancers	Primary T regulatory cells fromperipheralblood	blood
23	chr9:117631400-117633000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
24	chr9:117631600-117632200	Enhancers	Primary T cells from cord blood	blood
25	chr9:117631600-117632200	Enhancers	Adipose Nuclei	Adipose
26	chr9:117631600-117632600	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
27	chr9:117631600-117632600	Flanking Active TSS	Primary T killer memory cells from peripheral blood	blood
28	chr9:117631600-117632800	Enhancers	Primary B cells from cord blood	blood
29	chr9:117631600-117632800	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
30	chr9:117631600-117632800	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
31	chr9:117631600-117632800	Enhancers	Dnd41	blood
32	chr9:117631600-117632800	Enhancers	HepG2	liver
33	chr9:117631600-117633000	Enhancers	Primary B cells from peripheral blood	blood
34	chr9:117631600-117633200	Enhancers	Primary T cells fromperipheralblood	blood
35	chr9:117631600-117633200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
36	chr9:117631800-117632000	Enhancers	iPS-20b Cell Line	embryonic stem cell
37	chr9:117631800-117632600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr9:117631800-117632600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
39	chr9:117631800-117632600	Enhancers	iPS-18 Cell Line	embryonic stem cell
40	chr9:117631800-117632600	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
41	chr9:117631800-117632600	Enhancers	Lung	lung
42	chr9:117631800-117632800	Enhancers	H1 Cell Line	embryonic stem cell
43	chr9:117631800-117632800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
44	chr9:117631800-117632800	Enhancers	iPS-15b Cell Line	embryonic stem cell
45	chr9:117631800-117632800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
46	chr9:117631800-117632800	Enhancers	Fetal Thymus	thymus
47	chr9:117631800-117632800	Enhancers	Gastric	stomach
48	chr9:117631800-117632800	Enhancers	Rectal Mucosa Donor 31	rectum
49	chr9:117631800-117632800	Enhancers	Sigmoid Colon	Sigmoid Colon
50	chr9:117631800-117632800	Enhancers	Hela-S3	cervix

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