Variant report

Variant	nsv917735
Chromosome Location	chr9:140657466-140680648
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:450)
CpG islands
(count:671)
Chromatin interactive
region (count:16)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:450 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BCL11A	chr9:140674551-140675913	GM12878	blood:	n/a	n/a
2	BCL3	chr9:140674914-140675145	GM12878	blood:	n/a	n/a
3	BCL3	chr9:140675450-140675734	GM12878	blood:	n/a	n/a
4	BCL3	chr9:140675789-140676170	GM12878	blood:	n/a	n/a
5	BCL3	chr9:140674295-140674898	GM12878	blood:	n/a	n/a
6	BCL3	chr9:140675353-140676090	GM12878	blood:	n/a	n/a
7	BCL3	chr9:140676233-140676492	GM12878	blood:	n/a	n/a
8	BCL3	chr9:140674364-140675145	GM12878	blood:	n/a	n/a
9	BHLHE40	chr9:140680209-140680621	HepG2	liver:	n/a	n/a
10	BRCA1	chr9:140680050-140680233	HepG2	liver:	n/a	n/a
11	BRCA1	chr9:140668000-140668153	Hela-S3	cervix:	n/a	n/a
12	CEBPB	chr9:140680061-140680321	HepG2	liver:	n/a	chr9:140680148-140680159
13	CEBPB	chr9:140674203-140674497	IMR90	lung:	n/a	chr9:140674358-140674371
14	CEBPB	chr9:140674267-140674478	A549	lung:	n/a	chr9:140674358-140674371
15	CEBPB	chr9:140674234-140674467	HepG2	liver:	n/a	chr9:140674358-140674371
16	CHD2	chr9:140670794-140670803	HepG2	liver:	n/a	n/a
17	CREB1	chr9:140656680-140657483	GM12878	blood:	n/a	n/a
18	CREB1	chr9:140656711-140657483	GM12878	blood:	n/a	n/a
19	CTCF	chr9:140680240-140680390	HCPEpiC	choroid plexus:	n/a	n/a
20	CTCF	chr9:140667040-140667190	HUVEC	blood vessel:	n/a	chr9:140667134-140667147
21	CTCF	chr9:140667080-140667230	AG09319	gingival:	n/a	chr9:140667134-140667147
22	CTCF	chr9:140667080-140667230	A549	lung:	n/a	chr9:140667134-140667147
23	CTCF	chr9:140658840-140658990	GM12864	blood:	n/a	n/a
24	CTCF	chr9:140673013-140673114	GM19239	blood:	n/a	chr9:140673054-140673075
25	CTCF	chr9:140667060-140667210	HCT-116	colon:	n/a	chr9:140667134-140667147
26	CTCF	chr9:140667100-140667250	GM12865	blood:	n/a	chr9:140667134-140667147
27	CTCF	chr9:140667080-140667230	HPAF	blood vessel:	n/a	chr9:140667134-140667147
28	CTCF	chr9:140667080-140667230	HEEpiC	esophagus:	n/a	chr9:140667134-140667147
29	CTCF	chr9:140666882-140667392	MCF-7	breast:	n/a	chr9:140667134-140667147
30	CTCF	chr9:140667080-140667230	GM12866	blood:	n/a	chr9:140667134-140667147
31	CTCF	chr9:140667040-140667223	HepG2	liver:	n/a	chr9:140667134-140667147
32	CTCF	chr9:140667120-140667270	HRE	kidney:	n/a	chr9:140667134-140667147
33	CTCF	chr9:140667100-140667250	HRE	kidney:	n/a	chr9:140667134-140667147
34	CTCF	chr9:140680235-140680336	HepG2	liver:	n/a	n/a
35	CTCF	chr9:140667000-140667150	AG09319	gingival:	n/a	chr9:140667134-140667147
36	CTCF	chr9:140673071-140673077	GM19240	blood:	n/a	n/a
37	CTCF	chr9:140680260-140680410	HPF	lung:	n/a	n/a
38	CTCF	chr9:140680260-140680410	HFF	foreskin:	n/a	n/a
39	CTCF	chr9:140667040-140667190	GM12873	blood:	n/a	chr9:140667134-140667147
40	CTCF	chr9:140667080-140667230	AG04449	skin:	n/a	chr9:140667134-140667147
41	CTCF	chr9:140667060-140667210	SAEC	small airway:	n/a	chr9:140667134-140667147
42	CTCF	chr9:140667060-140667210	HVMF	connective:	n/a	chr9:140667134-140667147
43	CTCF	chr9:140666940-140667090	A549	lung:	n/a	n/a
44	CTCF	chr9:140667069-140667216	GM10266	blood:	n/a	chr9:140667134-140667147
45	CTCF	chr9:140667051-140667263	H1-hESC	embryonic stem cell:	n/a	chr9:140667134-140667147
46	CTCF	chr9:140667120-140667270	AG04450	lung:	n/a	chr9:140667134-140667147
47	CTCF	chr9:140667040-140667190	HA-sp	spinal cord:	n/a	chr9:140667134-140667147
48	CTCF	chr9:140667000-140667150	AG04450	lung:	n/a	chr9:140667134-140667147
49	CTCF	chr9:140680240-140680390	HepG2	liver:	n/a	n/a
50	CTCF	chr9:140659660-140659810	AG09319	gingival:	n/a	n/a

(count:671 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:140658436-140658486	PrEC	prostate:	n/a
2	chr9:140671632-140671682	Hepatocyte	liver:	n/a
3	chr9:140674013-140674063	PFSK-1	brain:	n/a
4	chr9:140674013-140674063	BJ	skin:	n/a
5	chr9:140658436-140658486	HL-60	blood:	n/a
6	chr9:140675616-140675666	HRPEpiC	eye:	n/a
7	chr9:140680393-140680443	PrEC	prostate:	n/a
8	chr9:140680393-140680443	PANC-1	pancreas:	n/a
9	chr9:140675616-140675666	HMEC	breast:	n/a
10	chr9:140680393-140680443	HCT-116	colon:	n/a
11	chr9:140673936-140673986	Caco-2	colon:	n/a
12	chr9:140671200-140671250	BJ	skin:	n/a
13	chr9:140675616-140675666	PFSK-1	brain:	n/a
14	chr9:140658436-140658486	GM12878	blood:	n/a
15	chr9:140676141-140676191	Jurkat	blood:	n/a
16	chr9:140671200-140671250	K562	blood:	n/a
17	chr9:140675929-140675979	SK-N-SH_RA	brain:	n/a
18	chr9:140675616-140675666	PANC-1	pancreas:	n/a
19	chr9:140678883-140678933	BE2_C	brain:	n/a
20	chr9:140678883-140678933	HCPEpiC	choroid plexus:	n/a
21	chr9:140676141-140676191	AG09309	skin:	n/a
22	chr9:140658436-140658486	SK-N-SH_RA	brain:	n/a
23	chr9:140658436-140658486	H1-hESC	embryonic stem cell:	embryo
24	chr9:140674013-140674063	HCM	heart:	n/a
25	chr9:140675616-140675666	HRCEpiC	kidney:	n/a
26	chr9:140676853-140676903	Jurkat	blood:	n/a
27	chr9:140674013-140674063	MCF10A-Er-Src	breast:	n/a
28	chr9:140680393-140680443	NB4	blood:	n/a
29	chr9:140675616-140675666	HCT-116	colon:	n/a
30	chr9:140680393-140680443	NT2-D1	testis:	n/a
31	chr9:140675929-140675979	PFSK-1	brain:	n/a
32	chr9:140676853-140676903	HIPEpiC	eye:	n/a
33	chr9:140671632-140671682	ovcar-3	ovarian:	n/a
34	chr9:140658436-140658486	AG09319	gingival:	n/a
35	chr9:140676853-140676903	HPAEpiC	pulmonary alveolar:	n/a
36	chr9:140658436-140658486	PFSK-1	brain:	n/a
37	chr9:140673936-140673986	GM19239	blood:	n/a
38	chr9:140676141-140676191	HMEC	breast:	n/a
39	chr9:140671632-140671682	NH-A	brain:	n/a
40	chr9:140680393-140680443	HMEC	breast:	n/a
41	chr9:140676853-140676903	Caco-2	colon:	n/a
42	chr9:140673936-140673986	NHDF-neo	bronchial:	n/a
43	chr9:140671200-140671250	AoSMC	blood vessel:	n/a
44	chr9:140676141-140676191	MCF-7	breast:	n/a
45	chr9:140678883-140678933	HEEpiC	esophagus:	n/a
46	chr9:140674013-140674063	AG04450	lung:	fetal
47	chr9:140675616-140675666	Hela-S3	cervix:	n/a
48	chr9:140671200-140671250	HCPEpiC	choroid plexus:	n/a
49	chr9:140671632-140671682	ECC-1	luminal epithelium:	n/a
50	chr9:140671632-140671682	SK-N-MC	brain:	n/a

(count:16 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:140667645..140669335-chr9:140669650..140672274,2	K562	blood:
2	chr9:140667022..140668743-chr9:140670497..140672972,3	MCF-7	breast:
3	chr9:140672962..140675618-chr9:140678748..140680768,2	K562	blood:
4	chr9:140656494..140658049-chr9:140665141..140666954,2	MCF-7	breast:
5	chr9:140512733..140514752-chr9:140658191..140660880,2	MCF-7	breast:
6	chr9:140672962..140675618-chr9:140678748..140680768,2	K562	blood:
7	chr9:140662415..140665334-chr9:140667330..140669473,2	MCF-7	breast:
8	chr9:140667645..140669335-chr9:140669650..140672274,2	K562	blood:
9	chr9:140667022..140668743-chr9:140670497..140672972,3	MCF-7	breast:
10	chr9:140656494..140658049-chr9:140665141..140666954,2	MCF-7	breast:
11	chr9:140662415..140665334-chr9:140667330..140669473,2	MCF-7	breast:
12	chr9:140499260..140502923-chr9:140667967..140671652,3	MCF-7	breast:
13	chr9:140679440..140682132-chr9:140702994..140705523,2	K562	blood:
14	chr9:140649627..140652485-chr9:140655729..140657732,2	MCF-7	breast:
15	chr9:140675774..140679711-chr9:140680099..140683198,4	K562	blood:
16	chr9:140591766..140593331-chr9:140667353..140669493,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CACNA1B-4	chr9:140657474-140659224	NONHSAT135751

No data

Variant related genes	Relation type
EHMT1	TF binding region
EHMT1	CpG island
ENSG00000255585	chromatin interactions
ENSG00000181090	chromatin interactions
ENSG00000197070	chromatin interactions
ENSG00000203993	chromatin interactions

Extended variants
information (count: 1080 )
Associated
traits (count: 20 )

Variant overlapped rSNPs/rCNVs (count:1080 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs549974321	chr9:140657553-140657554	Strong transcription ZNF genes & repeats Genic enhancers Weak transcription Transcr. at gene 5' and 3'	lncRNA	n/a	Overlapped CNVs	n/a
2	rs570141785	chr9:140657586-140657587	Strong transcription ZNF genes & repeats Genic enhancers Weak transcription Transcr. at gene 5' and 3'	lncRNA	n/a	Overlapped CNVs	n/a
3	rs537995112	chr9:140657593-140657594	Strong transcription ZNF genes & repeats Genic enhancers Weak transcription Transcr. at gene 5' and 3'	lncRNA	n/a	Overlapped CNVs	n/a
4	rs554349034	chr9:140657602-140657603	Strong transcription ZNF genes & repeats Genic enhancers Weak transcription Transcr. at gene 5' and 3'	lncRNA	n/a	Overlapped CNVs	n/a
5	rs574409336	chr9:140657605-140657606	Strong transcription ZNF genes & repeats Genic enhancers Weak transcription Transcr. at gene 5' and 3'	lncRNA	n/a	Overlapped CNVs	n/a
6	rs71499182	chr9:140657628-140657629	Strong transcription ZNF genes & repeats Genic enhancers Weak transcription Transcr. at gene 5' and 3'	lncRNA	n/a	Overlapped CNVs	n/a
7	rs151021520	chr9:140657636-140657637	Strong transcription ZNF genes & repeats Genic enhancers Weak transcription Transcr. at gene 5' and 3'	lncRNA	n/a	Overlapped CNVs	n/a
8	rs57849153	chr9:140657637-140657638	Strong transcription ZNF genes & repeats Genic enhancers Weak transcription Transcr. at gene 5' and 3'	lncRNA	n/a	Overlapped CNVs	n/a
9	rs533786300	chr9:140657643-140657644	Strong transcription ZNF genes & repeats Genic enhancers Weak transcription Transcr. at gene 5' and 3'	lncRNA	n/a	Overlapped CNVs	n/a
10	rs553776619	chr9:140657653-140657654	Strong transcription ZNF genes & repeats Genic enhancers Weak transcription Transcr. at gene 5' and 3'	lncRNA	n/a	Overlapped CNVs	n/a
11	rs577213879	chr9:140657660-140657661	Strong transcription ZNF genes & repeats Genic enhancers Weak transcription Transcr. at gene 5' and 3'	lncRNA	n/a	Overlapped CNVs	n/a
12	rs72766947	chr9:140657676-140657677	Strong transcription ZNF genes & repeats Genic enhancers Weak transcription Transcr. at gene 5' and 3'	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs150458864	chr9:140657698-140657699	Strong transcription ZNF genes & repeats Genic enhancers Weak transcription Transcr. at gene 5' and 3'	lncRNA	n/a	Overlapped CNVs	n/a
14	rs576153217	chr9:140657723-140657724	Strong transcription ZNF genes & repeats Genic enhancers Weak transcription Transcr. at gene 5' and 3'	lncRNA	n/a	Overlapped CNVs	n/a
15	rs138254095	chr9:140657757-140657758	Strong transcription ZNF genes & repeats Genic enhancers Weak transcription Transcr. at gene 5' and 3'	lncRNA	n/a	Overlapped CNVs	n/a
16	rs149594396	chr9:140657760-140657761	Strong transcription ZNF genes & repeats Genic enhancers Weak transcription Transcr. at gene 5' and 3'	lncRNA	n/a	Overlapped CNVs	n/a
17	rs571881252	chr9:140657780-140657781	Strong transcription ZNF genes & repeats Genic enhancers Weak transcription Transcr. at gene 5' and 3'	lncRNA	n/a	Overlapped CNVs	n/a
18	rs11137207	chr9:140657825-140657826	Strong transcription ZNF genes & repeats Weak transcription Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
19	rs559729220	chr9:140657882-140657883	Strong transcription ZNF genes & repeats Weak transcription Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
20	rs73574192	chr9:140657897-140657898	Strong transcription ZNF genes & repeats Weak transcription Genic enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs11137208	chr9:140657950-140657951	Strong transcription ZNF genes & repeats Weak transcription Genic enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs533488033	chr9:140657967-140657968	Strong transcription ZNF genes & repeats Weak transcription Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
23	rs7018624	chr9:140657971-140657972	Strong transcription ZNF genes & repeats Weak transcription Genic enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
24	rs7864181	chr9:140657973-140657974	Strong transcription ZNF genes & repeats Weak transcription Genic enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs529452454	chr9:140657981-140657982	Strong transcription ZNF genes & repeats Weak transcription Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
26	rs147280179	chr9:140657996-140657997	Strong transcription ZNF genes & repeats Weak transcription Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
27	rs557438846	chr9:140658036-140658037	Strong transcription ZNF genes & repeats Genic enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
28	rs139124162	chr9:140658052-140658053	Strong transcription ZNF genes & repeats Genic enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
29	rs374514184	chr9:140658061-140658062	Strong transcription ZNF genes & repeats Genic enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
30	rs143043943	chr9:140658065-140658066	Strong transcription ZNF genes & repeats Genic enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
31	rs574075254	chr9:140658087-140658088	Strong transcription ZNF genes & repeats Genic enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
32	rs539790679	chr9:140658094-140658095	Strong transcription ZNF genes & repeats Genic enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
33	rs147456168	chr9:140658147-140658148	Strong transcription ZNF genes & repeats Genic enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
34	rs367912770	chr9:140658174-140658175	Strong transcription ZNF genes & repeats Genic enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
35	rs576217510	chr9:140658175-140658176	Strong transcription ZNF genes & repeats Genic enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
36	rs536611595	chr9:140658181-140658182	Strong transcription ZNF genes & repeats Genic enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
37	rs182391412	chr9:140658197-140658198	Strong transcription ZNF genes & repeats Genic enhancers Weak transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
38	rs555509343	chr9:140658221-140658222	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
39	rs572208229	chr9:140658250-140658251	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
40	rs112486678	chr9:140658265-140658266	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
41	rs541120272	chr9:140658305-140658306	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
42	rs564190013	chr9:140658332-140658333	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
43	rs148691274	chr9:140658336-140658337	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
44	rs544132651	chr9:140658350-140658351	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
45	rs3125798	chr9:140658364-140658365	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region lncRNA	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs529563535	chr9:140658382-140658383	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
47	rs549316567	chr9:140658405-140658406	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
48	rs186943791	chr9:140658406-140658407	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
49	rs142196975	chr9:140658416-140658417	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
50	rs569895098	chr9:140658424-140658425	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:20)

Disease	PMID	Source
Leukemia	17361228	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Glioblastoma	16823260	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Cardiac fibroma	18329553	CNVD
Lung cancer	19147751	CNVD
Cervical cancer	17311676	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Gastric cancer	17908304	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Salivary gland adenoid cystic carcinoma	17545515	CNVD
Chordoma	18071362	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Sudden cardiac death	19188705	CNVD
Myoepithelioma	18604193	CNVD
Tuberous sclerosis	19566914	CNVD
Multiple myeloma	16616336	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Mantle cell lymphoma	19029149	CNVD
Breast cancer	21509527	CNVD

Chromatin state (count:888 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:140633800-140663000	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
2	chr9:140637200-140666800	Strong transcription	Dnd41	blood
3	chr9:140640200-140674800	Strong transcription	HUES48 Cell Line	embryonic stem cell
4	chr9:140643000-140666600	Strong transcription	iPS-20b Cell Line	embryonic stem cell
5	chr9:140646000-140662800	Strong transcription	Hela-S3	cervix
6	chr9:140646400-140659200	Strong transcription	Rectal Mucosa Donor 31	rectum
7	chr9:140646600-140657800	Strong transcription	Foreskin Melanocyte Primary Cells skin01	Skin
8	chr9:140647400-140662800	Strong transcription	Fetal Intestine Large	intestine
9	chr9:140648600-140659400	Strong transcription	HepG2	liver
10	chr9:140649800-140663000	Strong transcription	Placenta	Placenta
11	chr9:140649800-140712400	Weak transcription	Psoas Muscle	Psoas
12	chr9:140650000-140679200	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
13	chr9:140650200-140658800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
14	chr9:140650200-140661200	Weak transcription	Right Atrium	heart
15	chr9:140650200-140662600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr9:140650200-140662600	Strong transcription	Primary hematopoietic stem cells	blood
17	chr9:140650200-140662600	Strong transcription	Thymus	Thymus
18	chr9:140650200-140663000	Strong transcription	Primary monocytes fromperipheralblood	blood
19	chr9:140650200-140663000	Strong transcription	Rectal Mucosa Donor 29	rectum
20	chr9:140650200-140663200	Strong transcription	Fetal Intestine Small	intestine
21	chr9:140650200-140663200	Strong transcription	Fetal Stomach	stomach
22	chr9:140650200-140664000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
23	chr9:140650200-140666000	Strong transcription	Primary neutrophils fromperipheralblood	blood
24	chr9:140650200-140678800	Strong transcription	Primary hematopoietic stem cells short term culture	blood
25	chr9:140650200-140682600	Strong transcription	Monocytes-CD14+_RO01746	blood
26	chr9:140650200-140700000	Strong transcription	Primary T cells from cord blood	blood
27	chr9:140650400-140659600	Strong transcription	Brain Germinal Matrix	brain
28	chr9:140650400-140662800	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
29	chr9:140650400-140664000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chr9:140650400-140673400	Weak transcription	Fetal Brain Male	brain
31	chr9:140651600-140665800	Strong transcription	HUES6 Cell Line	embryonic stem cell
32	chr9:140652000-140659000	Strong transcription	Fetal Brain Female	brain
33	chr9:140652000-140662000	Strong transcription	Stomach Smooth Muscle	stomach
34	chr9:140652000-140673400	Weak transcription	Fetal Heart	heart
35	chr9:140652200-140658000	Strong transcription	Gastric	stomach
36	chr9:140652200-140660600	Strong transcription	Right Ventricle	heart
37	chr9:140652200-140676600	Weak transcription	Pancreatic Islets	Pancreatic Islet
38	chr9:140652400-140658600	Strong transcription	Liver	Liver
39	chr9:140652800-140659800	Strong transcription	NHEK	skin
40	chr9:140652800-140662800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
41	chr9:140653000-140658800	Weak transcription	Stomach Mucosa	stomach
42	chr9:140653000-140662800	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
43	chr9:140653000-140664800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
44	chr9:140653800-140659000	Genic enhancers	Spleen	Spleen
45	chr9:140653800-140661400	Weak transcription	HUVEC	blood vessel
46	chr9:140654000-140672000	Weak transcription	NHDF-Ad	bronchial
47	chr9:140654400-140659000	Genic enhancers	Fetal Adrenal Gland	Adrenal Gland
48	chr9:140654600-140658000	Weak transcription	Fetal Kidney	kidney
49	chr9:140654600-140662800	Strong transcription	Cortex derived primary cultured neurospheres	brain
50	chr9:140654800-140658800	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived

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