Variant report

Variant	nsv615198
Chromosome Location	chr9:115397206-115589251
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3442)
CpG islands
(count:856)
Chromatin interactive
region (count:220)
LncRNA
region (count:10)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:3442 , 50 per page) page: 1 2 3 4 5 6 7 ... 69

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:115512431-115512988	HepG2	liver:	n/a	n/a
2	ARID3A	chr9:115480237-115480501	HepG2	liver:	n/a	n/a
3	ARID3A	chr9:115480303-115480518	K562	blood:	n/a	n/a
4	ARID3A	chr9:115480786-115481091	HepG2	liver:	n/a	n/a
5	ARID3A	chr9:115512832-115512868	K562	blood:	n/a	n/a
6	ARID3A	chr9:115526787-115526979	K562	blood:	n/a	n/a
7	ARID3A	chr9:115509251-115509790	HepG2	liver:	n/a	n/a
8	ARID3A	chr9:115494056-115494755	HepG2	liver:	n/a	n/a
9	ARID3A	chr9:115527085-115527557	HepG2	liver:	n/a	n/a
10	ARID3A	chr9:115479963-115479990	K562	blood:	n/a	n/a
11	ATF1	chr9:115492920-115493063	K562	blood:	n/a	n/a
12	ATF1	chr9:115546849-115547018	K562	blood:	n/a	n/a
13	ATF1	chr9:115479899-115480664	K562	blood:	n/a	n/a
14	ATF2	chr9:115571553-115572322	GM12878	blood:	n/a	n/a
15	ATF2	chr9:115571491-115572271	GM12878	blood:	n/a	n/a
16	ATF2	chr9:115480059-115480571	H1-hESC	embryonic stem cell:	n/a	n/a
17	ATF2	chr9:115546557-115547024	H1-hESC	embryonic stem cell:	n/a	n/a
18	ATF2	chr9:115546485-115546980	H1-hESC	embryonic stem cell:	n/a	n/a
19	ATF2	chr9:115536387-115537342	GM12878	blood:	n/a	n/a
20	ATF2	chr9:115479969-115480608	GM12878	blood:	n/a	n/a
21	ATF2	chr9:115461429-115461926	GM12878	blood:	n/a	n/a
22	ATF2	chr9:115479964-115480574	H1-hESC	embryonic stem cell:	n/a	n/a
23	ATF2	chr9:115534041-115534389	GM12878	blood:	n/a	n/a
24	ATF2	chr9:115461473-115461858	GM12878	blood:	n/a	n/a
25	ATF2	chr9:115533877-115534620	GM12878	blood:	n/a	n/a
26	ATF3	chr9:115513811-115514038	K562	blood:	n/a	chr9:115513959-115513968
27	ATF3	chr9:115512764-115513021	K562	blood:	n/a	n/a
28	BACH1	chr9:115513425-115513999	H1-hESC	embryonic stem cell:	n/a	n/a
29	BACH1	chr9:115555648-115555803	H1-hESC	embryonic stem cell:	n/a	n/a
30	BACH1	chr9:115480800-115481000	H1-hESC	embryonic stem cell:	n/a	n/a
31	BACH1	chr9:115480689-115480847	K562	blood:	n/a	n/a
32	BATF	chr9:115477422-115477655	GM12878	blood:	n/a	n/a
33	BATF	chr9:115571596-115572164	GM12878	blood:	n/a	chr9:115571860-115571871
34	BATF	chr9:115477441-115477621	GM12878	blood:	n/a	n/a
35	BATF	chr9:115555592-115555842	GM12878	blood:	n/a	n/a
36	BATF	chr9:115481521-115481962	GM12878	blood:	n/a	n/a
37	BATF	chr9:115481594-115481937	GM12878	blood:	n/a	n/a
38	BATF	chr9:115571549-115572196	GM12878	blood:	n/a	chr9:115571860-115571871
39	BATF	chr9:115450305-115450695	GM12878	blood:	n/a	chr9:115450534-115450545 chr9:115450535-115450545
40	BCL11A	chr9:115571502-115572209	GM12878	blood:	n/a	n/a
41	BCL11A	chr9:115571550-115572162	GM12878	blood:	n/a	n/a
42	BCL3	chr9:115461526-115461832	GM12878	blood:	n/a	n/a
43	BCL3	chr9:115571588-115572096	GM12878	blood:	n/a	n/a
44	BCLAF1	chr9:115555367-115555922	GM12878	blood:	n/a	n/a
45	BCLAF1	chr9:115571542-115572234	GM12878	blood:	n/a	n/a
46	BCLAF1	chr9:115479865-115480402	GM12878	blood:	n/a	n/a
47	BCLAF1	chr9:115461422-115462143	GM12878	blood:	n/a	n/a
48	BCLAF1	chr9:115479702-115480535	GM12878	blood:	n/a	chr9:115480429-115480442
49	BCLAF1	chr9:115582032-115582507	GM12878	blood:	n/a	n/a
50	BCLAF1	chr9:115536629-115537207	GM12878	blood:	n/a	n/a

(count:856 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:115512530-115512580	HRPEpiC	eye:	n/a
2	chr9:115512530-115512580	AG09309	skin:	n/a
3	chr9:115512530-115512580	HRPEpiC	eye:	n/a
4	chr9:115512530-115512580	AG09309	skin:	n/a
5	chr9:115513525-115513575	HepG2	liver:	n/a
6	chr9:115513820-115513870	IMR90	lung:	fetal
7	chr9:115481039-115481089	PrEC	prostate:	n/a
8	chr9:115509770-115509820	HRE	kidney:	n/a
9	chr9:115480630-115480680	CMK	blood:	n/a
10	chr9:115509770-115509820	MCF-7	breast:	n/a
11	chr9:115481039-115481089	HRCEpiC	kidney:	n/a
12	chr9:115509770-115509820	SK-N-SH	brain:	n/a
13	chr9:115480625-115480675	HNPCEpiC	eye:	n/a
14	chr9:115513525-115513575	MCF-7	breast:	n/a
15	chr9:115513056-115513106	SK-N-MC	brain:	n/a
16	chr9:115513525-115513575	Caco-2	colon:	n/a
17	chr9:115480324-115480374	ovcar-3	ovarian:	n/a
18	chr9:115480324-115480374	HNPCEpiC	eye:	n/a
19	chr9:115512612-115512662	IMR90	lung:	fetal
20	chr9:115481039-115481089	GM06990	blood:	n/a
21	chr9:115480630-115480680	Hela-S3	cervix:	n/a
22	chr9:115513756-115513806	ProgFib	skin:	n/a
23	chr9:115480539-115480589	HRCEpiC	kidney:	n/a
24	chr9:115513820-115513870	CMK	blood:	n/a
25	chr9:115513820-115513870	HCPEpiC	choroid plexus:	n/a
26	chr9:115513756-115513806	ECC-1	luminal epithelium:	n/a
27	chr9:115513820-115513870	SK-N-MC	brain:	n/a
28	chr9:115512530-115512580	BJ	skin:	n/a
29	chr9:115509770-115509820	PFSK-1	brain:	n/a
30	chr9:115480630-115480680	MCF10A-Er-Src	breast:	n/a
31	chr9:115513056-115513106	NHBE	bronchial:	n/a
32	chr9:115513525-115513575	HIPEpiC	eye:	n/a
33	chr9:115480324-115480374	IMR90	lung:	fetal
34	chr9:115480324-115480374	HCF	heart:	n/a
35	chr9:115512612-115512662	HMEC	breast:	n/a
36	chr9:115480324-115480374	HUVEC	blood vessel:	n/a
37	chr9:115480625-115480675	IMR90	lung:	fetal
38	chr9:115480060-115480110	SK-N-MC	brain:	n/a
39	chr9:115513482-115513532	NT2-D1	testis:	n/a
40	chr9:115480324-115480374	AG10803	skin:	n/a
41	chr9:115513756-115513806	HCPEpiC	choroid plexus:	n/a
42	chr9:115513820-115513870	T-47D	breast:	n/a
43	chr9:115480539-115480589	PrEC	prostate:	n/a
44	chr9:115513056-115513106	HRPEpiC	eye:	n/a
45	chr9:115481039-115481089	LNCaP	prostate:	n/a
46	chr9:115513756-115513806	H1-hESC	embryonic stem cell:	embryo
47	chr9:115512530-115512580	AG04450	lung:	fetal
48	chr9:115513056-115513106	ECC-1	luminal epithelium:	n/a
49	chr9:115480539-115480589	GM06990	blood:	n/a
50	chr9:115509770-115509820	Caco-2	colon:	n/a

(count:220 , 50 per page) page: 1 2 3 4 5

No.	Distal block	Cell Line	Cell type
1	chr9:115478793..115482013-chr9:115511686..115514694,6	MCF-7	breast:
2	chr9:115555053..115556635-chr9:115557312..115560299,2	MCF-7	breast:
3	chr9:115472706..115474595-chr9:115477328..115479365,2	K562	blood:
4	chr9:115473082..115474008-chr9:115511306..115512239,2	K562	blood:
5	chr9:115574660..115576391-chr9:115583184..115586176,2	K562	blood:
6	chr9:115511487..115514115-chr9:115544583..115546972,6	MCF-7	breast:
7	chr9:115401662..115403762-chr9:115408579..115410766,2	K562	blood:
8	chr3:47822834..47823428-chr9:115479877..115480684,2	Hela-S3	cervix:
9	chr9:115205537..115206125-chr9:115473120..115473635,2	MCF-7	breast:
10	chr9:115565373..115568100-chr9:115582412..115584863,2	MCF-7	breast:
11	chr9:115449599..115451431-chr9:115473540..115475115,2	K562	blood:
12	chr9:115457896..115460451-chr9:115510686..115513121,2	K562	blood:
13	chr9:115505654..115506184-chr9:115665140..115665712,2	MCF-7	breast:
14	chr9:115476453..115479133-chr9:115517930..115520835,2	MCF-7	breast:
15	chr9:115205263..115206168-chr9:115581964..115582608,2	MCF-7	breast:
16	chr9:115475870..115478172-chr9:115478861..115481812,2	K562	blood:
17	chr9:115571216..115573226-chr9:115575838..115578800,2	K562	blood:
18	chr9:115247524..115250431-chr9:115478767..115481765,2	MCF-7	breast:
19	chr9:115586128..115587696-chr9:115592074..115593808,2	MCF-7	breast:
20	chr9:115545454..115548524-chr9:115549503..115552233,3	MCF-7	breast:
21	chr9:115537609..115539652-chr9:115540859..115543192,2	K562	blood:
22	chr9:115568430..115571071-chr9:115577497..115580948,3	MCF-7	breast:
23	chr9:115512683..115513666-chr9:115555193..115556149,4	MCF-7	breast:
24	chr9:115512316..115514216-chr9:115529153..115530836,3	MCF-7	breast:
25	chr9:115425694..115427398-chr9:115429129..115432033,2	K562	blood:
26	chr9:115469893..115474595-chr9:115477865..115481972,7	K562	blood:
27	chr9:115205105..115205795-chr9:115467855..115468653,2	MCF-7	breast:
28	chr9:115512668..115515460-chr9:115534425..115536617,2	K562	blood:
29	chr9:115449599..115451431-chr9:115473540..115475115,2	K562	blood:
30	chr9:115513405..115514933-chr9:115545989..115548662,2	MCF-7	breast:
31	chr9:115534861..115537925-chr9:115540163..115544235,3	MCF-7	breast:
32	chr9:115512640..115515348-chr9:115547273..115548788,2	MCF-7	breast:
33	chr9:115456646..115458575-chr9:115460716..115463371,2	MCF-7	breast:
34	chr9:115555096..115556091-chr9:115581952..115582779,4	MCF-7	breast:
35	chr9:115488383..115489985-chr9:115491570..115493098,2	K562	blood:
36	chr9:115465512..115468135-chr9:115469344..115471975,2	MCF-7	breast:
37	chr9:115496362..115497969-chr9:115509483..115511853,2	K562	blood:
38	chr9:115533346..115535894-chr9:115545369..115547662,2	MCF-7	breast:
39	chr9:115465064..115467730-chr9:115468816..115472137,3	K562	blood:
40	chr9:115555506..115558401-chr9:115567192..115568729,2	MCF-7	breast:
41	chr9:115555053..115556635-chr9:115557312..115560299,2	MCF-7	breast:
42	chr9:115224285..115224817-chr9:115427888..115428611,2	MCF-7	breast:
43	chr9:115581292..115584107-chr9:115597875..115599534,2	MCF-7	breast:
44	chr9:115566617..115568493-chr9:115570718..115573933,3	K562	blood:
45	chr9:115205603..115206463-chr9:115425836..115426747,2	MCF-7	breast:
46	chr9:115479584..115483073-chr9:115511753..115516407,5	MCF-7	breast:
47	chr9:115507468..115509112-chr9:115510847..115513004,2	K562	blood:
48	chr9:115555372..115556213-chr9:115581844..115582573,3	MCF-7	breast:
49	chr9:115425089..115427194-chr9:115429213..115432033,2	K562	blood:
50	chr9:115578144..115579912-chr9:115585850..115587895,2	K562	blood:

(count:10 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KIAA1958-1	chr9:115454118-115454181	NONHSAT134022
2	lnc-SLC46A2-4	chr9:115456314-115456513	NONHSAT134023
3	lnc-SLC46A2-4	chr9:115478741-115478821	NONHSAT134023
4	lnc-C9orf80-1	chr9:115511360-115512795	XLOC_007830
5	lnc-C9orf80-1	chr9:115505051-115505514	XLOC_007830
6	lnc-KIAA1958-1	chr9:115453057-115453265	NONHSAT134022
7	lnc-C9orf80-1	chr9:115512686-115512736	XLOC_007830
8	lnc-C9orf80-1	chr9:115511182-115511550	XLOC_007830
9	lnc-SLC46A2-4	chr9:115480267-115480397	NONHSAT134023
10	lnc-KIAA1958-1	chr9:115484007-115484956	NONHSAT134022

No data

Variant related genes	Relation type
ENSG00000226609	TF binding region
INIP	TF binding region
SNX30	TF binding region
ENSG00000226609	CpG island
INIP	CpG island
SNX30	CpG island
ENSG00000101144	chromatin interactions
ENSG00000150760	chromatin interactions
ENSG00000119314	chromatin interactions
ENSG00000230185	chromatin interactions
ENSG00000271631	chromatin interactions
ENSG00000226609	chromatin interactions
ENSG00000165185	chromatin interactions
ENSG00000010165	chromatin interactions
ENSG00000049239	chromatin interactions
ENSG00000110925	chromatin interactions
ENSG00000148158	chromatin interactions
ENSG00000119471	chromatin interactions
ENSG00000148153	chromatin interactions
ENSG00000173473	chromatin interactions
SETD8	miRNA target sites

Extended variants
information (count: 7079 )
Associated
traits (count: 55 )

Variant overlapped rSNPs/rCNVs (count:7079 , 50 per page) page: 1 2 3 4 5 6 7 ... 142

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11789059	chr9:115397206-115397207	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs146634627	chr9:115397213-115397214	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs530253836	chr9:115397250-115397251	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs114681771	chr9:115397252-115397253	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs560801105	chr9:115397271-115397272	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs141257991	chr9:115397304-115397305	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs73656439	chr9:115397338-115397339	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs551398705	chr9:115397351-115397352	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs113134925	chr9:115397373-115397374	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs571179207	chr9:115397383-115397384	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs78166483	chr9:115397390-115397391	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs552804596	chr9:115397392-115397393	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs78342688	chr9:115397405-115397406	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs552052615	chr9:115397433-115397434	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs373435040	chr9:115397495-115397496	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs573976523	chr9:115397501-115397502	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs3983383	chr9:115397538-115397539	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs530635868	chr9:115397544-115397545	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs199927885	chr9:115397545-115397546	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs28671461	chr9:115397557-115397558	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs567004187	chr9:115397595-115397596	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs146824551	chr9:115397615-115397616	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs140482714	chr9:115397638-115397639	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs566963894	chr9:115397654-115397655	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs11793489	chr9:115397721-115397722	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs10981461	chr9:115397770-115397771	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs191681648	chr9:115397798-115397799	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs568208755	chr9:115397821-115397822	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs75319344	chr9:115397868-115397869	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs555032352	chr9:115397877-115397878	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs184893767	chr9:115397896-115397897	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs540387097	chr9:115397905-115397906	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs535302452	chr9:115397974-115397975	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs565729442	chr9:115397979-115397980	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs536206262	chr9:115397992-115397993	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs554844093	chr9:115398024-115398025	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs559459033	chr9:115398037-115398038	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs572958734	chr9:115398068-115398069	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs553532049	chr9:115398089-115398090	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs187463911	chr9:115398175-115398176	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs564831609	chr9:115398195-115398196	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs140095675	chr9:115398230-115398231	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs530749665	chr9:115398238-115398239	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs565841720	chr9:115398278-115398279	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs560570255	chr9:115398305-115398306	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs555863903	chr9:115398353-115398354	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs10981462	chr9:115398381-115398382	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs376716398	chr9:115398386-115398387	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs201809065	chr9:115398387-115398388	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs113783354	chr9:115398388-115398389	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:55)

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
Breast cancer	22522925	CNVD
Melanoma	20877625	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:4710 , 50 per page) page: 1 2 3 4 5 6 7 ... 95

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:115379000-115410200	Weak transcription	HSMMtube	muscle
2	chr9:115381000-115402800	Weak transcription	Primary T cells from cord blood	blood
3	chr9:115381200-115400600	Weak transcription	Fetal Intestine Small	intestine
4	chr9:115381200-115401600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr9:115381200-115401600	Weak transcription	Dnd41	blood
6	chr9:115383000-115399800	Weak transcription	Gastric	stomach
7	chr9:115383600-115401400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
8	chr9:115387600-115401400	Weak transcription	Esophagus	oesophagus
9	chr9:115388000-115401400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
10	chr9:115392400-115401400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr9:115392400-115401400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr9:115392400-115415600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
13	chr9:115392400-115421600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
14	chr9:115392600-115401200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
15	chr9:115392600-115401400	Weak transcription	H1 Cell Line	embryonic stem cell
16	chr9:115392600-115401600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr9:115392600-115401600	Weak transcription	Fetal Stomach	stomach
18	chr9:115392600-115410400	Weak transcription	Ovary	ovary
19	chr9:115394200-115401400	Weak transcription	Primary B cells from cord blood	blood
20	chr9:115397800-115408000	Weak transcription	HepG2	liver
21	chr9:115398200-115401400	Weak transcription	Fetal Intestine Large	intestine
22	chr9:115398200-115401800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
23	chr9:115399200-115401200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr9:115399800-115400000	Enhancers	Gastric	stomach
25	chr9:115400000-115401600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr9:115400000-115401600	Weak transcription	Gastric	stomach
27	chr9:115400600-115403000	ZNF genes & repeats	Fetal Intestine Small	intestine
28	chr9:115401200-115402200	ZNF genes & repeats	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
29	chr9:115401200-115403000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr9:115401200-115426200	Weak transcription	Fetal Kidney	kidney
31	chr9:115401400-115402000	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
32	chr9:115401400-115402000	ZNF genes & repeats	Esophagus	oesophagus
33	chr9:115401400-115402200	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
34	chr9:115401400-115402200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
35	chr9:115401400-115402400	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr9:115401400-115402800	ZNF genes & repeats	Fetal Intestine Large	intestine
37	chr9:115401400-115403000	ZNF genes & repeats	Primary B cells from cord blood	blood
38	chr9:115401400-115403200	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
39	chr9:115401400-115403200	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
40	chr9:115401600-115401800	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr9:115401600-115401800	Genic enhancers	Gastric	stomach
42	chr9:115401600-115401800	Enhancers	Pancreas	Pancrea
43	chr9:115401600-115402000	ZNF genes & repeats	Aorta	Aorta
44	chr9:115401600-115402200	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
45	chr9:115401600-115402400	ZNF genes & repeats	Monocytes-CD14+_RO01746	blood
46	chr9:115401600-115402600	ZNF genes & repeats	Dnd41	blood
47	chr9:115401600-115403000	ZNF genes & repeats	H9 Derived Neuron Cultured Cells	ES cell derived
48	chr9:115401600-115403000	ZNF genes & repeats	Fetal Lung	lung
49	chr9:115401600-115403000	ZNF genes & repeats	Fetal Stomach	stomach
50	chr9:115401800-115402200	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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