Variant report

Variant	nsv438108
Chromosome Location	chr9:86488586-86542206
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1382)
CpG islands
(count:429)
Chromatin interactive
region (count:38)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1382 , 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	chr9:86500378-86500758	HepG2	liver:	n/a	n/a
2	ARID3A	chr9:86535494-86536921	HepG2	liver:	n/a	n/a
3	ATF2	chr9:86535464-86536111	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr9:86535405-86536155	GM12878	blood:	n/a	n/a
5	ATF2	chr9:86535487-86536085	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr9:86535356-86536066	GM12878	blood:	n/a	n/a
7	ATF3	chr9:86500485-86500713	K562	blood:	n/a	n/a
8	ATF3	chr9:86500470-86500690	HepG2	liver:	n/a	n/a
9	BACH1	chr9:86535776-86536716	H1-hESC	embryonic stem cell:	n/a	n/a
10	BATF	chr9:86535650-86536027	GM12878	blood:	n/a	n/a
11	BCL11A	chr9:86535684-86536658	GM12878	blood:	n/a	chr9:86536409-86536422 chr9:86536253-86536266
12	BCL11A	chr9:86535614-86536076	GM12878	blood:	n/a	n/a
13	BCL3	chr9:86540372-86540633	GM12878	blood:	n/a	n/a
14	BCL3	chr9:86535616-86536060	GM12878	blood:	n/a	n/a
15	BCLAF1	chr9:86535428-86536097	GM12878	blood:	n/a	n/a
16	BCLAF1	chr9:86536451-86536976	GM12878	blood:	n/a	n/a
17	BCLAF1	chr9:86535470-86536149	GM12878	blood:	n/a	n/a
18	BCLAF1	chr9:86536317-86536801	GM12878	blood:	n/a	chr9:86536409-86536422
19	BCLAF1	chr9:86535622-86536069	K562	blood:	n/a	n/a
20	BCLAF1	chr9:86535488-86536083	K562	blood:	n/a	n/a
21	BHLHE40	chr9:86535531-86536682	K562	blood:	n/a	n/a
22	BHLHE40	chr9:86535528-86536878	GM12878	blood:	n/a	n/a
23	BHLHE40	chr9:86535661-86536005	HepG2	liver:	n/a	n/a
24	BHLHE40	chr9:86535574-86535894	A549	lung:	n/a	n/a
25	BHLHE40	chr9:86535499-86536393	HepG2	liver:	n/a	n/a
26	BRCA1	chr9:86536506-86536561	GM12878	blood:	n/a	n/a
27	BRCA1	chr9:86536303-86536529	H1-hESC	embryonic stem cell:	n/a	n/a
28	BRCA1	chr9:86536286-86536806	Hela-S3	cervix:	n/a	n/a
29	CBX3	chr9:86535301-86536803	HCT-116	colon:	n/a	n/a
30	CBX3	chr9:86535560-86536100	K562	blood:	n/a	n/a
31	CBX3	chr9:86536379-86536702	K562	blood:	n/a	n/a
32	CBX3	chr9:86535625-86536005	K562	blood:	n/a	n/a
33	CCNT2	chr9:86535846-86536660	K562	blood:	n/a	chr9:86536060-86536069 chr9:86536448-86536457 chr9:86536142-86536151
34	CEBPB	chr9:86500450-86500768	A549	lung:	n/a	chr9:86500602-86500613
35	CEBPB	chr9:86509271-86509565	HepG2	liver:	n/a	n/a
36	CEBPB	chr9:86500493-86500746	MCF-7	breast:	n/a	chr9:86500602-86500613
37	CEBPB	chr9:86498732-86498910	HepG2	liver:	n/a	chr9:86498787-86498798
38	CEBPB	chr9:86536573-86536921	K562	blood:	n/a	chr9:86536760-86536771
39	CEBPB	chr9:86535915-86536013	K562	blood:	n/a	n/a
40	CEBPB	chr9:86500482-86500757	MCF-7	breast:	n/a	chr9:86500602-86500613
41	CEBPB	chr9:86500416-86500715	K562	blood:	n/a	chr9:86500602-86500613
42	CEBPB	chr9:86498682-86498899	Hela-S3	cervix:	n/a	chr9:86498787-86498798
43	CEBPB	chr9:86536530-86536956	K562	blood:	n/a	chr9:86536760-86536771
44	CEBPB	chr9:86500458-86500744	HepG2	liver:	n/a	chr9:86500602-86500613
45	CEBPB	chr9:86500453-86500751	HepG2	liver:	n/a	chr9:86500602-86500613
46	CEBPB	chr9:86500493-86500905	A549	lung:	n/a	chr9:86500602-86500613
47	CEBPB	chr9:86535109-86535274	H1-hESC	embryonic stem cell:	n/a	n/a
48	CEBPB	chr9:86536536-86536926	HepG2	liver:	n/a	chr9:86536760-86536771
49	CEBPB	chr9:86535922-86536094	HepG2	liver:	n/a	n/a
50	CEBPB	chr9:86535550-86537011	Hela-S3	cervix:	n/a	chr9:86536760-86536771

(count:429 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:86536513-86536563	SK-N-SH	brain:	n/a
2	chr9:86538824-86538874	K562	blood:	n/a
3	chr9:86536513-86536563	SK-N-SH	brain:	n/a
4	chr9:86538824-86538874	K562	blood:	n/a
5	chr9:86538824-86538874	Hepatocyte	liver:	n/a
6	chr9:86535572-86535622	AG09319	gingival:	n/a
7	chr9:86535572-86535622	AoSMC	blood vessel:	n/a
8	chr9:86536043-86536093	SAEC	small airway:	n/a
9	chr9:86536028-86536078	GM19239	blood:	n/a
10	chr9:86535572-86535622	HCT-116	colon:	n/a
11	chr9:86536043-86536093	MCF-7	breast:	n/a
12	chr9:86536513-86536563	Hela-S3	cervix:	n/a
13	chr9:86535755-86535805	K562	blood:	n/a
14	chr9:86536028-86536078	Hela-S3	cervix:	n/a
15	chr9:86538824-86538874	HCF	heart:	n/a
16	chr9:86536043-86536093	CMK	blood:	n/a
17	chr9:86536513-86536563	T-47D	breast:	n/a
18	chr9:86536028-86536078	GM06990	blood:	n/a
19	chr9:86535695-86535745	GM06990	blood:	n/a
20	chr9:86535755-86535805	HUVEC	blood vessel:	n/a
21	chr9:86535755-86535805	MCF-7	breast:	n/a
22	chr9:86536028-86536078	MCF10A-Er-Src	breast:	n/a
23	chr9:86536043-86536093	SKMC	muscle:	n/a
24	chr9:86538824-86538874	PrEC	prostate:	n/a
25	chr9:86538824-86538874	SAEC	small airway:	n/a
26	chr9:86538824-86538874	IMR90	lung:	fetal
27	chr9:86535695-86535745	Hepatocyte	liver:	n/a
28	chr9:86536043-86536093	Jurkat	blood:	n/a
29	chr9:86536043-86536093	K562	blood:	n/a
30	chr9:86536028-86536078	NHDF-neo	bronchial:	n/a
31	chr9:86535755-86535805	AG04450	lung:	fetal
32	chr9:86535572-86535622	BJ	skin:	n/a
33	chr9:86538824-86538874	HRE	kidney:	n/a
34	chr9:86535695-86535745	ProgFib	skin:	n/a
35	chr9:86536513-86536563	HRPEpiC	eye:	n/a
36	chr9:86538824-86538874	GM06990	blood:	n/a
37	chr9:86535695-86535745	HEK293	kidney:	embryo
38	chr9:86536028-86536078	AG09319	gingival:	n/a
39	chr9:86535572-86535622	PrEC	prostate:	n/a
40	chr9:86535572-86535622	SAEC	small airway:	n/a
41	chr9:86536043-86536093	U87	brain:	n/a
42	chr9:86535755-86535805	GM12878	blood:	n/a
43	chr9:86535755-86535805	GM06990	blood:	n/a
44	chr9:86535572-86535622	GM12878	blood:	n/a
45	chr9:86536043-86536093	AG09319	gingival:	n/a
46	chr9:86535695-86535745	GM12878	blood:	n/a
47	chr9:86535695-86535745	K562	blood:	n/a
48	chr9:86535695-86535745	HNPCEpiC	eye:	n/a
49	chr9:86536043-86536093	HCF	heart:	n/a
50	chr9:86536028-86536078	Caco-2	colon:	n/a

(count:38 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:51705086..51705705-chr9:86536186..86536829,2	HCT-116	colon:
2	chr9:86534561..86538164-chr9:86570673..86573880,3	K562	blood:
3	chr6:74230441..74231008-chr9:86535957..86536568,2	Hela-S3	cervix:
4	chr9:86536152..86538297-chr9:86540828..86543846,3	MCF-7	breast:
5	chr9:86542024..86543859-chr9:86595135..86597329,2	MCF-7	breast:
6	chr9:86321248..86324502-chr9:86534491..86537588,5	MCF-7	breast:
7	chr9:86534814..86537259-chr9:86954011..86956598,2	MCF-7	breast:
8	chr9:86534003..86537844-chr9:86570557..86574103,8	K562	blood:
9	chr9:86321176..86323111-chr9:86534764..86537575,5	MCF-7	breast:
10	chr9:86430622..86432919-chr9:86535075..86537489,2	MCF-7	breast:
11	chr14:105940614..105941354-chr9:86535879..86536754,2	MCF-7	breast:
12	chr9:86431003..86433746-chr9:86534377..86536332,2	K562	blood:
13	chr9:86533247..86537973-chr9:86593370..86597981,20	MCF-7	breast:
14	chr9:86533979..86537502-chr9:86594012..86596999,11	MCF-7	breast:
15	chr9:86535600..86536226-chr9:86875793..86876638,2	K562	blood:
16	chr9:86321510..86324086-chr9:86534187..86535894,2	K562	blood:
17	chr9:86507562..86509693-chr9:86509764..86511267,2	K562	blood:
18	chr9:86531254..86532896-chr9:86534357..86536311,2	MCF-7	breast:
19	chr9:86535411..86537432-chr9:127629716..127632471,2	MCF-7	breast:
20	chr9:86541635..86544345-chr9:86665548..86667347,2	K562	blood:
21	chr9:86533593..86537892-chr9:86593047..86598677,10	K562	blood:
22	chr12:73941837..73944242-chr9:86536650..86538183,2	MCF-7	breast:
23	chr9:86535076..86537991-chr9:86590146..86593000,2	K562	blood:
24	chr9:86529939..86532744-chr9:86534062..86535993,2	MCF-7	breast:
25	chr9:86525950..86529688-chr9:86534412..86537158,4	MCF-7	breast:
26	chr9:86534520..86537940-chr9:86592614..86595774,6	K562	blood:
27	chr9:86237285..86238795-chr9:86535469..86537545,2	K562	blood:
28	chr5:110848126..110849104-chr9:86535767..86536636,2	Hela-S3	cervix:
29	chr9:86535234..86536021-chr9:86875727..86876675,2	MCF-7	breast:
30	chr9:86507562..86509693-chr9:86509764..86511267,2	K562	blood:
31	chr1:28974640..28975500-chr9:86535654..86536400,2	Hela-S3	cervix:
32	chr9:86534503..86538702-chr9:86568820..86574555,7	MCF-7	breast:
33	chr9:86535347..86536164-chr9:86929967..86930640,3	MCF-7	breast:
34	chr9:86236616..86242493-chr9:86533666..86537484,7	MCF-7	breast:
35	chr9:86237271..86239294-chr9:86534482..86537409,3	MCF-7	breast:
36	chr9:86499637..86502408-chr9:86534472..86537007,2	MCF-7	breast:
37	chr9:86451626..86452376-chr9:86520762..86521311,2	MCF-7	breast:
38	chr9:86531254..86532896-chr9:86534357..86536311,2	MCF-7	breast:

No data

Variant related genes	Relation type
KIF27	TF binding region
KIF27	CpG island
ENSG00000164081	chromatin interactions
ENSG00000182809	chromatin interactions
ENSG00000165118	chromatin interactions
ENSG00000254473	chromatin interactions
ENSG00000165115	chromatin interactions
ENSG00000156508	chromatin interactions
ENSG00000165119	chromatin interactions
ENSG00000226877	chromatin interactions
ENSG00000136950	chromatin interactions
ENSG00000164211	chromatin interactions
ENSG00000165113	chromatin interactions
ENSG00000197506	chromatin interactions
ENSG00000178966	chromatin interactions
ENSG00000135018	chromatin interactions
ENSG00000270103	chromatin interactions
ENSG00000148057	chromatin interactions

Extended variants
information (count: 2008 )
Associated
traits (count: 73 )

Variant overlapped rSNPs/rCNVs (count:2008 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7853625	chr9:86488586-86488587	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs568023233	chr9:86488587-86488588	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs565918526	chr9:86488592-86488593	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs530610876	chr9:86488660-86488661	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs539128921	chr9:86488711-86488712	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs149084542	chr9:86488735-86488736	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs143206784	chr9:86488740-86488741	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs543418650	chr9:86488749-86488750	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs554982159	chr9:86488752-86488753	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs574786931	chr9:86488761-86488762	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs542142869	chr9:86488781-86488782	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs186680275	chr9:86488782-86488783	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs527894572	chr9:86488798-86488799	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs369313435	chr9:86488833-86488834	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs148268695	chr9:86488891-86488892	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs564607465	chr9:86488892-86488893	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs531567003	chr9:86488899-86488900	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs550407317	chr9:86488956-86488957	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs75498380	chr9:86488966-86488967	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs80058047	chr9:86488967-86488968	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs569799644	chr9:86488973-86488974	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs58189689	chr9:86488977-86488978	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs550146166	chr9:86489022-86489023	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs568495340	chr9:86489023-86489024	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs529188306	chr9:86489061-86489062	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs538713243	chr9:86489087-86489088	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs192359555	chr9:86489106-86489107	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs147450042	chr9:86489172-86489173	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs539625321	chr9:86489194-86489195	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs138406868	chr9:86489225-86489226	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs569726566	chr9:86489242-86489243	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs147300547	chr9:86489258-86489259	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs140970659	chr9:86489289-86489290	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs149402154	chr9:86489305-86489306	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs11140280	chr9:86489306-86489307	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs183815342	chr9:86489308-86489309	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs188781993	chr9:86489564-86489565	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs554063710	chr9:86489565-86489566	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs558806871	chr9:86489641-86489642	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs139201309	chr9:86489646-86489647	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs564565054	chr9:86489658-86489659	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs192900943	chr9:86489675-86489676	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs547907697	chr9:86489706-86489707	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs566019508	chr9:86489707-86489708	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs185054565	chr9:86489708-86489709	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs543969063	chr9:86489711-86489712	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs144068362	chr9:86489727-86489728	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs146450788	chr9:86489788-86489789	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs535859570	chr9:86489848-86489849	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs34762926	chr9:86489849-86489850	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:73)

Disease	PMID	Source
Chordoma	18071362	CNVD
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
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
Urothelial carcinoma	21177765	CNVD
Renal cell carcinoma	21668985	CNVD
Autism	22495311	CNVD
Melanoma	18172304	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
Leukemia	18688285	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
Acute promyelocytic leukemia	19109227	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute myeloid leukemia	21251322	CNVD
Hepatocellular carcinoma	16750200	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	17603634	CNVD
Acute myeloid leukemia	20729466	CNVD
Oral cancer	21386901	CNVD
Glioblastoma multiforme	21750150	CNVD
Cancer	21183584	CNVD
Bipolar disorder	18458673	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Wilms tumour	21544195	CNVD
Prostate cancer	18632612	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Gastric cancer	17908304	CNVD
Urothelial cell carcinoma	18451213	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Renal cell carcinoma	18765545	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Glioblastoma multiforme	22286061	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:577 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:86460600-86518200	Weak transcription	Thymus	Thymus
2	chr9:86461600-86535400	Weak transcription	Fetal Intestine Small	intestine
3	chr9:86461600-86535400	Weak transcription	Ovary	ovary
4	chr9:86462200-86535200	Weak transcription	Fetal Brain Female	brain
5	chr9:86462600-86499200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
6	chr9:86462600-86500600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr9:86462600-86503800	Weak transcription	Dnd41	blood
8	chr9:86462600-86535200	Weak transcription	Brain Anterior Caudate	brain
9	chr9:86462800-86515000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
10	chr9:86462800-86518000	Weak transcription	Fetal Intestine Large	intestine
11	chr9:86462800-86518000	Weak transcription	Fetal Stomach	stomach
12	chr9:86481000-86535800	Weak transcription	Sigmoid Colon	Sigmoid Colon
13	chr9:86482000-86518000	Weak transcription	Left Ventricle	heart
14	chr9:86486600-86494400	Weak transcription	Aorta	Aorta
15	chr9:86490400-86490800	Enhancers	Fetal Heart	heart
16	chr9:86490400-86510800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
17	chr9:86491000-86495600	Weak transcription	Small Intestine	intestine
18	chr9:86491000-86535200	Weak transcription	Duodenum Smooth Muscle	Duodenum
19	chr9:86491200-86502200	Weak transcription	Brain Germinal Matrix	brain
20	chr9:86491200-86535200	Weak transcription	Primary hematopoietic stem cells	blood
21	chr9:86491400-86518000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
22	chr9:86491800-86518200	Weak transcription	Primary B cells from cord blood	blood
23	chr9:86492000-86500600	Weak transcription	Fetal Lung	lung
24	chr9:86493600-86500000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
25	chr9:86495000-86518000	Weak transcription	Primary T cells from cord blood	blood
26	chr9:86496000-86535000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr9:86496200-86496400	Enhancers	Hela-S3	cervix
28	chr9:86496400-86497000	Enhancers	HMEC	breast
29	chr9:86496400-86500400	Weak transcription	Hela-S3	cervix
30	chr9:86496400-86533000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
31	chr9:86496600-86515600	Weak transcription	Rectal Mucosa Donor 31	rectum
32	chr9:86497000-86497400	Weak transcription	HMEC	breast
33	chr9:86497200-86497800	Enhancers	NHEK	skin
34	chr9:86497400-86497600	Enhancers	HMEC	breast
35	chr9:86497600-86499800	Weak transcription	HMEC	breast
36	chr9:86497800-86500200	Weak transcription	NHEK	skin
37	chr9:86498800-86504000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
38	chr9:86499200-86500000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
39	chr9:86499200-86500800	Weak transcription	Duodenum Mucosa	Duodenum
40	chr9:86499200-86513400	Weak transcription	Fetal Muscle Trunk	muscle
41	chr9:86499400-86501600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr9:86499400-86518200	Weak transcription	Fetal Muscle Leg	muscle
43	chr9:86499400-86535000	Weak transcription	Fetal Kidney	kidney
44	chr9:86499800-86501400	Enhancers	HUVEC	blood vessel
45	chr9:86499800-86501800	Enhancers	Muscle Satellite Cultured Cells	--
46	chr9:86499800-86501800	Enhancers	HMEC	breast
47	chr9:86499800-86523200	Weak transcription	Fetal Thymus	thymus
48	chr9:86500000-86500400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
49	chr9:86500000-86501400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
50	chr9:86500000-86501800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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