Variant report

Variant	nsv6680
Chromosome Location	chr9:117690388-117699304
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	BHLHE40	chr9:117692356-117693006	GM12878	blood:	n/a	n/a
2	CEBPB	chr9:117698888-117699167	IMR90	lung:	n/a	chr9:117699051-117699064 chr9:117699053-117699064 chr9:117699051-117699064 chr9:117699053-117699064 chr9:117699051-117699062
3	CEBPB	chr9:117698894-117699181	Hela-S3	cervix:	n/a	chr9:117699051-117699064 chr9:117699053-117699064 chr9:117699051-117699064 chr9:117699053-117699064 chr9:117699051-117699062
4	CEBPB	chr9:117698979-117699179	K562	blood:	n/a	chr9:117699051-117699064 chr9:117699053-117699064 chr9:117699051-117699064 chr9:117699053-117699064 chr9:117699051-117699062
5	CEBPB	chr9:117699109-117699132	H1-hESC	embryonic stem cell:	n/a	n/a
6	CEBPB	chr9:117698979-117699174	A549	lung:	n/a	chr9:117699051-117699064 chr9:117699053-117699064 chr9:117699051-117699064 chr9:117699053-117699064 chr9:117699051-117699062
7	CEBPB	chr9:117698945-117699106	HepG2	liver:	n/a	chr9:117699051-117699064 chr9:117699053-117699064 chr9:117699051-117699064 chr9:117699053-117699064 chr9:117699051-117699062
8	CREB1	chr9:117692710-117693052	GM12878	blood:	n/a	n/a
9	CTCF	chr9:117697787-117697881	IMR90	lung:	n/a	n/a
10	CTCF	chr9:117697760-117697910	HPF	lung:	n/a	n/a
11	CTCF	chr9:117690460-117690610	A549	lung:	n/a	n/a
12	CTCF	chr9:117692947-117693004	Spleen_OC	spleen:	n/a	n/a
13	CTCF	chr9:117692820-117692934	Fibrobl	skin:	n/a	n/a
14	CTCF	chr9:117697700-117697850	HVMF	connective:	n/a	n/a
15	CTCF	chr9:117693497-117693589	GM19239	blood:	n/a	n/a
16	CTCF	chr9:117697740-117697890	AG04450	lung:	n/a	n/a
17	CTCF	chr9:117697660-117697810	AG04450	lung:	n/a	n/a
18	CTCF	chr9:117697780-117697930	NHDF-neo	bronchial:	n/a	n/a
19	CTCF	chr9:117697740-117697890	HVMF	connective:	n/a	n/a
20	EP300	chr9:117692846-117692949	GM12878	blood:	n/a	n/a
21	MYC	chr9:117693494-117693558	MCF-7	breast:	n/a	n/a
22	NRF1	chr9:117692823-117692961	GM12878	blood:	n/a	n/a
23	PAX5	chr9:117692809-117693032	GM12878	blood:	n/a	n/a
24	POLR2A	chr9:117698820-117699274	SK-N-MC	brain:	n/a	n/a
25	RUNX3	chr9:117692723-117693077	GM12878	blood:	n/a	n/a
26	RUNX3	chr9:117692278-117692652	GM12878	blood:	n/a	n/a
27	RUNX3	chr9:117692253-117692675	GM12878	blood:	n/a	n/a
28	RUNX3	chr9:117692749-117692967	GM12878	blood:	n/a	n/a
29	SPI1	chr9:117698974-117699289	HL-60	blood:	n/a	n/a
30	YY1	chr9:117692761-117693000	GM12892	blood:	n/a	n/a
31	ZNF384	chr9:117691508-117691818	GM12878	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:117692954-117693004	HNPCEpiC	eye:	n/a
2	chr9:117692954-117693004	BE2_C	brain:	n/a
3	chr9:117692745-117692795	HRCEpiC	kidney:	n/a
4	chr9:117694183-117694233	ProgFib	skin:	n/a
5	chr9:117692745-117692795	HepG2	liver:	n/a
6	chr9:117693010-117693060	MCF10A-Er-Src	breast:	n/a
7	chr9:117694183-117694233	PFSK-1	brain:	n/a
8	chr9:117692954-117693004	GM12878	blood:	n/a
9	chr9:117692954-117693004	HCF	heart:	n/a
10	chr9:117694183-117694233	A549	lung:	n/a
11	chr9:117692954-117693004	AG09309	skin:	n/a
12	chr9:117692745-117692795	GM19239	blood:	n/a
13	chr9:117693010-117693060	HCT-116	colon:	n/a
14	chr9:117694183-117694233	RPTEC	kidney:	n/a
15	chr9:117693010-117693060	PFSK-1	brain:	n/a
16	chr9:117692954-117693004	HAEpiC	amniotic membrane:	n/a
17	chr9:117694183-117694233	HL-60	blood:	n/a
18	chr9:117692745-117692795	GM12891	blood:	n/a
19	chr9:117692745-117692795	IMR90	lung:	fetal
20	chr9:117693010-117693060	NB4	blood:	n/a
21	chr9:117694183-117694233	SK-N-SH_RA	brain:	n/a
22	chr9:117692745-117692795	NHDF-neo	bronchial:	n/a
23	chr9:117693010-117693060	BJ	skin:	n/a
24	chr9:117694183-117694233	HRPEpiC	eye:	n/a
25	chr9:117694183-117694233	K562	blood:	n/a
26	chr9:117692745-117692795	SAEC	small airway:	n/a
27	chr9:117693010-117693060	Caco-2	colon:	n/a
28	chr9:117692745-117692795	HEEpiC	esophagus:	n/a
29	chr9:117694183-117694233	HCT-116	colon:	n/a
30	chr9:117693010-117693060	BE2_C	brain:	n/a
31	chr9:117694183-117694233	SK-N-MC	brain:	n/a
32	chr9:117692745-117692795	Hela-S3	cervix:	n/a
33	chr9:117692745-117692795	HNPCEpiC	eye:	n/a
34	chr9:117693010-117693060	AG04450	lung:	fetal
35	chr9:117693010-117693060	HCPEpiC	choroid plexus:	n/a
36	chr9:117693010-117693060	LNCaP	prostate:	n/a
37	chr9:117693010-117693060	HRCEpiC	kidney:	n/a
38	chr9:117692954-117693004	HUVEC	blood vessel:	n/a
39	chr9:117693010-117693060	NH-A	brain:	n/a
40	chr9:117692745-117692795	AG09319	gingival:	n/a
41	chr9:117692745-117692795	CMK	blood:	n/a
42	chr9:117692745-117692795	AG04449	skin:	fetal
43	chr9:117692954-117693004	GM12892	blood:	n/a
44	chr9:117694183-117694233	AG04450	lung:	fetal
45	chr9:117693010-117693060	AG10803	skin:	n/a
46	chr9:117692954-117693004	SK-N-SH_RA	brain:	n/a
47	chr9:117692954-117693004	HCT-116	colon:	n/a
48	chr9:117692954-117693004	PFSK-1	brain:	n/a
49	chr9:117692954-117693004	NH-A	brain:	n/a
50	chr9:117692954-117693004	HEK293	kidney:	embryo

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr9:117676811..117678604-chr9:117693310..117696147,2	MCF-7	breast:
2	chr9:117685063..117687885-chr9:117689510..117691619,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TNFSF8-2	chr9:117690365-117690580	l_3840_NR_024032

Variant related genes	Relation type
TNFSF8	TF binding region
TNFSF8	CpG island

Extended variants
information (count: 376 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:376 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs551758674	chr9:117690424-117690425	Weak transcription Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	lncRNA	n/a	Overlapped CNVs	n/a
2	rs370286018	chr9:117690581-117690582	Weak transcription Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
3	rs79152080	chr9:117690605-117690606	Weak transcription Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
4	rs543243075	chr9:117690612-117690613	Weak transcription Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
5	rs576165652	chr9:117690626-117690627	Weak transcription Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
6	rs34956779	chr9:117690636-117690637	Weak transcription Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
7	rs560132150	chr9:117690674-117690675	Weak transcription Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
8	rs142729797	chr9:117690690-117690691	Weak transcription Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
9	rs181884103	chr9:117690715-117690716	Weak transcription Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
10	rs76902137	chr9:117690732-117690733	Weak transcription Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
11	rs530493381	chr9:117690752-117690753	Weak transcription Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
12	rs10982456	chr9:117690758-117690759	Weak transcription Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs567307699	chr9:117690782-117690783	Weak transcription Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
14	rs573927738	chr9:117690804-117690805	Weak transcription Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
15	rs72756584	chr9:117690853-117690854	Weak transcription Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
16	rs2181032	chr9:117690864-117690865	Weak transcription Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs566463706	chr9:117690896-117690897	Weak transcription Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
18	rs376848292	chr9:117690928-117690929	Weak transcription Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
19	rs540733770	chr9:117690999-117691000	Weak transcription Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
20	rs151008332	chr9:117691041-117691042	Weak transcription Bivalent Enhancer Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
21	rs373494490	chr9:117691139-117691140	Weak transcription Bivalent Enhancer Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
22	rs1006025	chr9:117691201-117691202	Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs143169494	chr9:117691217-117691218	Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
24	rs554125769	chr9:117691226-117691227	Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
25	rs146653082	chr9:117691244-117691245	Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
26	rs557175842	chr9:117691258-117691259	Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
27	rs1006026	chr9:117691270-117691271	Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
28	rs140297778	chr9:117691275-117691276	Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
29	rs150316498	chr9:117691276-117691277	Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
30	rs1006027	chr9:117691313-117691314	Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs545733912	chr9:117691314-117691315	Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
32	rs565532927	chr9:117691318-117691319	Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
33	rs4978612	chr9:117691364-117691365	Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs538855834	chr9:117691389-117691390	Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
35	rs371189276	chr9:117691436-117691437	Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
36	rs1407303	chr9:117691441-117691442	Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
37	rs186902816	chr9:117691524-117691525	Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
38	rs3181360	chr9:117691558-117691559	Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs572345194	chr9:117691559-117691560	Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
40	rs566349450	chr9:117691568-117691569	Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
41	rs538410488	chr9:117691582-117691583	Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
42	rs374664793	chr9:117691637-117691638	Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
43	rs558582192	chr9:117691641-117691642	Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
44	rs79710528	chr9:117691654-117691655	Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
45	rs3181359	chr9:117691658-117691659	Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs562268712	chr9:117691659-117691660	Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
47	rs573728130	chr9:117691660-117691661	Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
48	rs75475737	chr9:117691676-117691677	Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
49	rs557310988	chr9:117691721-117691722	Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
50	rs574215667	chr9:117691764-117691765	Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:59)

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
Breast cancer	22522925	CNVD

Chromatin state (count:221 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:117673200-117692400	Weak transcription	Spleen	Spleen
2	chr9:117680200-117690400	Weak transcription	Fetal Thymus	thymus
3	chr9:117687800-117693400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr9:117688400-117693000	Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
5	chr9:117688600-117692800	Weak transcription	Fetal Lung	lung
6	chr9:117688800-117690400	Weak transcription	Primary B cells from peripheral blood	blood
7	chr9:117688800-117691000	Weak transcription	Placenta	Placenta
8	chr9:117689000-117693400	Active TSS	Thymus	Thymus
9	chr9:117689400-117690400	Enhancers	Primary hematopoietic stem cells	blood
10	chr9:117689400-117690600	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
11	chr9:117689400-117691200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
12	chr9:117689400-117691400	Flanking Active TSS	Primary T cells from cord blood	blood
13	chr9:117689400-117692000	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
14	chr9:117689400-117693600	Flanking Active TSS	Dnd41	blood
15	chr9:117689600-117690400	Enhancers	Primary neutrophils fromperipheralblood	blood
16	chr9:117689600-117690400	Flanking Active TSS	Primary T killer naive cells fromperipheralblood	blood
17	chr9:117689600-117690600	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
18	chr9:117689600-117690600	Flanking Active TSS	Primary T killer memory cells from peripheral blood	blood
19	chr9:117689600-117690600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
20	chr9:117689600-117690800	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
21	chr9:117689600-117690800	Flanking Active TSS	Primary mononuclear cells fromperipheralblood	Blood
22	chr9:117689600-117691400	Flanking Active TSS	Primary B cells from cord blood	blood
23	chr9:117689600-117692400	Active TSS	Primary T cells fromperipheralblood	blood
24	chr9:117689600-117692800	Transcr. at gene 5' and 3'	Primary T helper 17 cells PMA-I stimulated	--
25	chr9:117689600-117693000	Active TSS	Rectal Mucosa Donor 29	rectum
26	chr9:117689600-117693600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
27	chr9:117689800-117690400	Active TSS	Sigmoid Colon	Sigmoid Colon
28	chr9:117689800-117690600	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
29	chr9:117689800-117692800	Active TSS	Duodenum Mucosa	Duodenum
30	chr9:117689800-117693200	Active TSS	Adipose Nuclei	Adipose
31	chr9:117690000-117690400	Active TSS	Primary Natural Killer cells fromperipheralblood	blood
32	chr9:117690000-117692000	Active TSS	Duodenum Smooth Muscle	Duodenum
33	chr9:117690200-117690400	Active TSS	Primary hematopoietic stem cells short term culture	blood
34	chr9:117690200-117690600	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
35	chr9:117690200-117692400	Active TSS	Primary monocytes fromperipheralblood	blood
36	chr9:117690200-117692800	Active TSS	Liver	Liver
37	chr9:117690200-117692800	Active TSS	Rectal Mucosa Donor 31	rectum
38	chr9:117690200-117693000	Active TSS	Primary T helper memory cells from peripheral blood 2	blood
39	chr9:117690400-117690600	Active TSS	Primary T killer naive cells fromperipheralblood	blood
40	chr9:117690400-117690600	Flanking Active TSS	Sigmoid Colon	Sigmoid Colon
41	chr9:117690400-117690800	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
42	chr9:117690400-117690800	Flanking Active TSS	Primary Natural Killer cells fromperipheralblood	blood
43	chr9:117690400-117690800	Active TSS	Brain Hippocampus Middle	brain
44	chr9:117690400-117691000	Enhancers	Primary B cells from peripheral blood	blood
45	chr9:117690400-117691000	Flanking Active TSS	Primary hematopoietic stem cells	blood
46	chr9:117690400-117691000	Enhancers	Fetal Thymus	thymus
47	chr9:117690400-117691600	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
48	chr9:117690600-117690800	Active TSS	Primary T regulatory cells fromperipheralblood	blood
49	chr9:117690600-117690800	Flanking Active TSS	Primary T killer naive cells fromperipheralblood	blood
50	chr9:117690600-117690800	Active TSS	Sigmoid Colon	Sigmoid Colon

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