Variant report

Variant	nsv825069
Chromosome Location	chr9:123220951-123294240
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:781)
CpG islands
(count:61)
Chromatin interactive
region (count:47)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:781 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:123239872-123239944	HepG2	liver:	n/a	n/a
2	ARID3A	chr9:123243641-123243798	HepG2	liver:	n/a	n/a
3	ATF3	chr9:123286724-123286955	H1-hESC	embryonic stem cell:	n/a	n/a
4	BCL3	chr9:123239358-123239749	GM12878	blood:	n/a	n/a
5	BHLHE40	chr9:123260221-123260553	K562	blood:	n/a	n/a
6	BHLHE40	chr9:123239761-123239946	GM12878	blood:	n/a	n/a
7	BHLHE40	chr9:123239813-123239998	K562	blood:	n/a	n/a
8	BRCA1	chr9:123291381-123291533	H1-hESC	embryonic stem cell:	n/a	n/a
9	CBX3	chr9:123260086-123260472	K562	blood:	n/a	n/a
10	CEBPB	chr9:123239740-123240856	A549	lung:	n/a	chr9:123240004-123240012 chr9:123239787-123239798
11	CEBPB	chr9:123253467-123253857	A549	lung:	n/a	chr9:123253644-123253655
12	CEBPB	chr9:123240529-123240846	HepG2	liver:	n/a	n/a
13	CEBPB	chr9:123246500-123246645	H1-hESC	embryonic stem cell:	n/a	n/a
14	CEBPB	chr9:123286778-123287001	H1-hESC	embryonic stem cell:	n/a	chr9:123286866-123286877
15	CEBPB	chr9:123286811-123286910	K562	blood:	n/a	chr9:123286866-123286877
16	CEBPB	chr9:123284382-123284607	Hela-S3	cervix:	n/a	chr9:123284535-123284546
17	CEBPB	chr9:123253485-123253882	HepG2	liver:	n/a	chr9:123253644-123253655
18	CEBPB	chr9:123253567-123253793	ECC-1	luminal epithelium:	n/a	chr9:123253644-123253655
19	CEBPB	chr9:123237161-123237361	HepG2	liver:	n/a	chr9:123237247-123237258
20	CEBPB	chr9:123253556-123253809	MCF-7	breast:	n/a	chr9:123253644-123253655
21	CEBPB	chr9:123237102-123237460	Hela-S3	cervix:	n/a	chr9:123237247-123237258
22	CEBPB	chr9:123276234-123276521	A549	lung:	n/a	chr9:123276383-123276394
23	CEBPB	chr9:123284424-123284580	IMR90	lung:	n/a	chr9:123284535-123284546
24	CEBPB	chr9:123239694-123240890	IMR90	lung:	n/a	chr9:123240004-123240012 chr9:123239787-123239798
25	CEBPB	chr9:123276284-123276532	IMR90	lung:	n/a	chr9:123276383-123276394
26	CEBPB	chr9:123253495-123253885	K562	blood:	n/a	chr9:123253644-123253655
27	CEBPB	chr9:123237102-123237446	A549	lung:	n/a	chr9:123237247-123237258
28	CEBPB	chr9:123239771-123240904	Hela-S3	cervix:	n/a	chr9:123240004-123240012 chr9:123239787-123239798
29	CEBPB	chr9:123253495-123253890	H1-hESC	embryonic stem cell:	n/a	chr9:123253644-123253655
30	CEBPB	chr9:123286821-123286921	A549	lung:	n/a	chr9:123286866-123286877
31	CEBPB	chr9:123253487-123253904	IMR90	lung:	n/a	chr9:123253644-123253655
32	CEBPB	chr9:123239957-123240414	ECC-1	luminal epithelium:	n/a	chr9:123240004-123240012
33	CEBPB	chr9:123240128-123240308	K562	blood:	n/a	n/a
34	CEBPB	chr9:123240514-123240844	ECC-1	luminal epithelium:	n/a	n/a
35	CEBPB	chr9:123240485-123240869	ECC-1	luminal epithelium:	n/a	n/a
36	CEBPB	chr9:123276242-123276478	HepG2	liver:	n/a	chr9:123276383-123276394
37	CEBPB	chr9:123284437-123284682	HepG2	liver:	n/a	chr9:123284535-123284546
38	CEBPB	chr9:123253482-123253847	MCF-7	breast:	n/a	chr9:123253644-123253655
39	CEBPB	chr9:123284394-123284611	A549	lung:	n/a	chr9:123284535-123284546
40	CEBPB	chr9:123286788-123286967	HepG2	liver:	n/a	chr9:123286866-123286877
41	CEBPB	chr9:123276332-123276506	Hela-S3	cervix:	n/a	chr9:123276383-123276394
42	CEBPB	chr9:123239680-123240975	A549	lung:	n/a	chr9:123240004-123240012 chr9:123239787-123239798
43	CEBPB	chr9:123228991-123229199	HepG2	liver:	n/a	chr9:123229114-123229125
44	CEBPB	chr9:123253529-123253930	A549	lung:	n/a	chr9:123253644-123253655
45	CEBPB	chr9:123253467-123253906	Hela-S3	cervix:	n/a	chr9:123253644-123253655
46	CEBPB	chr9:123237090-123237890	IMR90	lung:	n/a	chr9:123237247-123237258
47	CEBPB	chr9:123253398-123253959	A549	lung:	n/a	chr9:123253644-123253655
48	CEBPB	chr9:123273180-123273380	Hela-S3	cervix:	n/a	n/a
49	CEBPB	chr9:123243370-123243871	HepG2	liver:	n/a	n/a
50	CEBPB	chr9:123229104-123229147	Hela-S3	cervix:	n/a	chr9:123229114-123229125

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:123257038-123257088	U87	brain:	n/a
2	chr9:123257038-123257088	AG04449	skin:	fetal
3	chr9:123257038-123257088	HEK293	kidney:	embryo
4	chr9:123257038-123257088	IMR90	lung:	fetal
5	chr9:123257038-123257088	HUVEC	blood vessel:	n/a
6	chr9:123257038-123257088	ECC-1	luminal epithelium:	n/a
7	chr9:123257038-123257088	MCF-7	breast:	n/a
8	chr9:123257038-123257088	HCM	heart:	n/a
9	chr9:123257038-123257088	HPAEpiC	pulmonary alveolar:	n/a
10	chr9:123257038-123257088	MCF10A-Er-Src	breast:	n/a
11	chr9:123257038-123257088	AG09319	gingival:	n/a
12	chr9:123257038-123257088	K562	blood:	n/a
13	chr9:123257038-123257088	LNCaP	prostate:	n/a
14	chr9:123257038-123257088	NHDF-neo	bronchial:	n/a
15	chr9:123257038-123257088	SK-N-SH	brain:	n/a
16	chr9:123257038-123257088	Hela-S3	cervix:	n/a
17	chr9:123257038-123257088	PFSK-1	brain:	n/a
18	chr9:123257038-123257088	HCPEpiC	choroid plexus:	n/a
19	chr9:123257038-123257088	Caco-2	colon:	n/a
20	chr9:123257038-123257088	CMK	blood:	n/a
21	chr9:123257038-123257088	SK-N-SH_RA	brain:	n/a
22	chr9:123257038-123257088	Jurkat	blood:	n/a
23	chr9:123257038-123257088	HepG2	liver:	n/a
24	chr9:123257038-123257088	PrEC	prostate:	n/a
25	chr9:123257038-123257088	HCT-116	colon:	n/a
26	chr9:123257038-123257088	HIPEpiC	eye:	n/a
27	chr9:123257038-123257088	GM19239	blood:	n/a
28	chr9:123257038-123257088	HMEC	breast:	n/a
29	chr9:123257038-123257088	HRE	kidney:	n/a
30	chr9:123257038-123257088	BE2_C	brain:	n/a
31	chr9:123257038-123257088	A549	lung:	n/a
32	chr9:123257038-123257088	HAEpiC	amniotic membrane:	n/a
33	chr9:123257038-123257088	NHBE	bronchial:	n/a
34	chr9:123257038-123257088	RPTEC	kidney:	n/a
35	chr9:123257038-123257088	HRPEpiC	eye:	n/a
36	chr9:123257038-123257088	BJ	skin:	n/a
37	chr9:123257038-123257088	GM06990	blood:	n/a
38	chr9:123257038-123257088	Hepatocyte	liver:	n/a
39	chr9:123257038-123257088	PANC-1	pancreas:	n/a
40	chr9:123257038-123257088	AG10803	skin:	n/a
41	chr9:123257038-123257088	GM12891	blood:	n/a
42	chr9:123257038-123257088	SK-N-MC	brain:	n/a
43	chr9:123257038-123257088	AoSMC	blood vessel:	n/a
44	chr9:123257038-123257088	H1-hESC	embryonic stem cell:	embryo
45	chr9:123257038-123257088	NB4	blood:	n/a
46	chr9:123257038-123257088	ProgFib	skin:	n/a
47	chr9:123257038-123257088	T-47D	breast:	n/a
48	chr9:123257038-123257088	AG04450	lung:	fetal
49	chr9:123257038-123257088	SAEC	small airway:	n/a
50	chr9:123257038-123257088	HCF	heart:	n/a

(count:47 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:123196041..123198829-chr9:123225952..123227681,2	K562	blood:
2	chr9:123234559..123236721-chr9:123239058..123241799,2	MCF-7	breast:
3	chr9:123282985..123285244-chr9:123341147..123343036,2	K562	blood:
4	chr9:123275107..123277193-chr9:123287758..123290308,2	MCF-7	breast:
5	chr9:123244669..123246921-chr9:123246964..123248594,2	MCF-7	breast:
6	chr1:14451774..14453737-chr9:123255451..123258036,2	MCF-7	breast:
7	chr9:123241147..123242931-chr9:123246454..123248810,2	K562	blood:
8	chr9:123224580..123226881-chr9:123229170..123231843,2	MCF-7	breast:
9	chr9:123235160..123237836-chr9:123239739..123242461,2	K562	blood:
10	chr9:123275107..123277193-chr9:123287758..123290308,2	MCF-7	breast:
11	chr9:123284465..123287463-chr9:123289215..123291184,2	K562	blood:
12	chr9:123280032..123282087-chr9:123283245..123285407,2	K562	blood:
13	chr9:123241277..123242854-chr9:123251171..123253174,2	K562	blood:
14	chr9:123246549..123250671-chr9:123252027..123255465,4	K562	blood:
15	chr9:123263216..123265024-chr9:123268935..123271826,2	MCF-7	breast:
16	chr9:123264422..123266542-chr9:123273482..123275479,2	K562	blood:
17	chr9:123246346..123249523-chr9:123250918..123254260,3	K562	blood:
18	chr9:123264422..123266542-chr9:123273482..123275479,2	K562	blood:
19	chr9:123278374..123280102-chr9:123280616..123283246,2	MCF-7	breast:
20	chr9:123230284..123234461-chr9:123234701..123237566,5	K562	blood:
21	chr9:123236194..123237805-chr9:123245359..123247095,2	K562	blood:
22	chr9:123287653..123290082-chr9:123297586..123299865,2	K562	blood:
23	chr9:123271955..123274624-chr9:123275742..123278633,2	K562	blood:
24	chr9:123223145..123226542-chr9:123234882..123237435,3	K562	blood:
25	chr9:123278374..123280102-chr9:123280616..123283246,2	MCF-7	breast:
26	chr9:123230284..123234461-chr9:123234701..123237566,5	K562	blood:
27	chr9:123236194..123237805-chr9:123245359..123247095,2	K562	blood:
28	chr9:123241277..123242854-chr9:123251171..123253174,2	K562	blood:
29	chr9:123270617..123272132-chr9:123336738..123338470,2	K562	blood:
30	chr9:123263216..123265024-chr9:123268935..123271826,2	MCF-7	breast:
31	chr9:123224416..123226142-chr9:123230567..123233122,2	K562	blood:
32	chr9:123241147..123242931-chr9:123246454..123248810,2	K562	blood:
33	chr9:123235160..123237836-chr9:123239739..123242461,2	K562	blood:
34	chr9:123271955..123274624-chr9:123275742..123278633,2	K562	blood:
35	chr9:123223145..123226542-chr9:123234882..123237435,3	K562	blood:
36	chr9:123244669..123246921-chr9:123246964..123248594,2	MCF-7	breast:
37	chr9:123284465..123287463-chr9:123289215..123291184,2	K562	blood:
38	chr9:123246549..123250671-chr9:123252027..123255465,4	K562	blood:
39	chr9:123269055..123271832-chr9:123289922..123291457,2	K562	blood:
40	chr9:123246346..123249523-chr9:123250918..123254260,3	K562	blood:
41	chr9:123224416..123226142-chr9:123230567..123233122,2	K562	blood:
42	chr9:123280032..123282087-chr9:123283245..123285407,2	K562	blood:
43	chr9:123269055..123271832-chr9:123289922..123291457,2	K562	blood:
44	chr9:123217720..123220736-chr9:123226690..123230371,4	K562	blood:
45	chr9:123234364..123235908-chr9:123238385..123240992,2	K562	blood:
46	chr9:123224580..123226881-chr9:123229170..123231843,2	MCF-7	breast:
47	chr9:123289526..123292255-chr9:123553519..123555739,2	MCF-7	breast:

No data

Variant related genes	Relation type
CDK5RAP2	TF binding region
CDK5RAP2	CpG island
ENSG00000136861	chromatin interactions
ENSG00000119402	chromatin interactions

Extended variants
information (count: 2507 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:2507 , 50 per page) page: 1 2 3 4 5 6 7 ... 51

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs182206268	chr9:123220970-123220971	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs185804121	chr9:123221003-123221004	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs111573035	chr9:123221043-123221044	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs149429216	chr9:123221059-123221060	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs377176749	chr9:123221074-123221075	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs558617493	chr9:123221108-123221109	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs372788555	chr9:123221248-123221249	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs577073934	chr9:123221276-123221277	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs540819238	chr9:123221280-123221281	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs572675295	chr9:123221301-123221302	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs553226324	chr9:123221318-123221319	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs74655660	chr9:123221328-123221329	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs544820839	chr9:123221453-123221454	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs115015407	chr9:123221480-123221481	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs148554919	chr9:123221501-123221502	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs115697890	chr9:123221564-123221565	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs564999851	chr9:123221569-123221570	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs556273485	chr9:123221597-123221598	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs191076696	chr9:123221612-123221613	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs544591227	chr9:123221681-123221682	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs564583957	chr9:123221756-123221757	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs373670478	chr9:123221773-123221774	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs561159286	chr9:123221799-123221800	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs528787497	chr9:123221804-123221805	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs530398393	chr9:123221880-123221881	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs527773975	chr9:123221881-123221882	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs547954051	chr9:123221894-123221895	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs568334446	chr9:123221912-123221913	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs577784235	chr9:123221973-123221974	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs529333527	chr9:123222127-123222128	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs144444426	chr9:123222138-123222139	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs547285472	chr9:123222158-123222159	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs375917930	chr9:123222199-123222200	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs539407181	chr9:123222204-123222205	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs558133034	chr9:123222205-123222206	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs570626923	chr9:123222212-123222213	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs534932608	chr9:123222215-123222216	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs553187571	chr9:123222218-123222219	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs78839589	chr9:123222263-123222264	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs541944119	chr9:123222294-123222295	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs557134616	chr9:123222297-123222298	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs575308624	chr9:123222308-123222309	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs545435333	chr9:123222451-123222452	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs564134164	chr9:123222535-123222536	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs76200896	chr9:123222551-123222552	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs540560958	chr9:123222569-123222570	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs561926312	chr9:123222587-123222588	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs183745139	chr9:123222588-123222589	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs146634921	chr9:123222591-123222592	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs141455368	chr9:123222641-123222642	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:60)

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
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
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
Melanoma	18172304	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	21509527	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Cervical cancer	16585170	CNVD
Ependymoma	19289631	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Gastric cancer	17908304	CNVD
Cervical cancer	17311676	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Neurodevelopmental disorder	22521361	CNVD
Melanoma	17363583	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:2586 , 50 per page) page: 1 2 3 4 5 6 7 ... 52

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:123193400-123223600	Strong transcription	Cortex derived primary cultured neurospheres	brain
2	chr9:123193400-123267600	Weak transcription	Pancreatic Islets	Pancreatic Islet
3	chr9:123195600-123224200	Strong transcription	HepG2	liver
4	chr9:123195600-123246600	Strong transcription	Dnd41	blood
5	chr9:123196200-123240400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr9:123198800-123247000	Strong transcription	Primary T cells from cord blood	blood
7	chr9:123201800-123240000	Strong transcription	Primary B cells from cord blood	blood
8	chr9:123202000-123236800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
9	chr9:123204800-123237000	Weak transcription	NHDF-Ad	bronchial
10	chr9:123206000-123233200	Weak transcription	Placenta Amnion	Placenta Amnion
11	chr9:123207000-123226200	Weak transcription	NHLF	lung
12	chr9:123207200-123239600	Strong transcription	Hela-S3	cervix
13	chr9:123208000-123248800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr9:123208800-123294200	Weak transcription	Stomach Mucosa	stomach
15	chr9:123209200-123225200	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
16	chr9:123209400-123241000	Strong transcription	Primary B cells from peripheral blood	blood
17	chr9:123209400-123242400	Strong transcription	Primary T helper cells fromperipheralblood	blood
18	chr9:123209600-123228000	Strong transcription	Monocytes-CD14+_RO01746	blood
19	chr9:123209600-123246800	Strong transcription	Primary T cells fromperipheralblood	blood
20	chr9:123210000-123239600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
21	chr9:123211000-123240000	Weak transcription	Psoas Muscle	Psoas
22	chr9:123212200-123254200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr9:123212400-123221000	Strong transcription	Rectal Mucosa Donor 31	rectum
24	chr9:123212400-123221600	Strong transcription	Fetal Thymus	thymus
25	chr9:123212600-123221000	Strong transcription	Muscle Satellite Cultured Cells	--
26	chr9:123212800-123224800	Strong transcription	Primary monocytes fromperipheralblood	blood
27	chr9:123213000-123222800	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
28	chr9:123213000-123223000	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
29	chr9:123213000-123223000	Strong transcription	Fetal Muscle Trunk	muscle
30	chr9:123213000-123223200	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
31	chr9:123213000-123224200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
32	chr9:123213200-123223200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
33	chr9:123214600-123223200	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
34	chr9:123214600-123223800	Strong transcription	Fetal Intestine Large	intestine
35	chr9:123214600-123224000	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
36	chr9:123214600-123224400	Strong transcription	Fetal Muscle Leg	muscle
37	chr9:123214800-123221000	Strong transcription	Fetal Intestine Small	intestine
38	chr9:123214800-123221600	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
39	chr9:123214800-123222400	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
40	chr9:123214800-123223000	Strong transcription	Duodenum Mucosa	Duodenum
41	chr9:123214800-123223200	Strong transcription	Adipose Nuclei	Adipose
42	chr9:123215000-123221800	Strong transcription	Liver	Liver
43	chr9:123215000-123223000	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
44	chr9:123215000-123224200	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
45	chr9:123215600-123222000	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
46	chr9:123215600-123222400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
47	chr9:123215800-123221200	Strong transcription	Foreskin Melanocyte Primary Cells skin01	Skin
48	chr9:123216000-123228400	Weak transcription	Gastric	stomach
49	chr9:123216000-123233200	Weak transcription	Small Intestine	intestine
50	chr9:123216200-123229000	Weak transcription	Esophagus	oesophagus

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