Variant report

Variant	nsv529440
Chromosome Location	chr9:140672499-140712604
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:645)
CpG islands
(count:1653)
Chromatin interactive
region (count:18)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:645 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr9:140710782-140711539	GM12878	blood:	n/a	n/a
2	ATF2	chr9:140703449-140703804	GM12878	blood:	n/a	n/a
3	ATF2	chr9:140710777-140711402	GM12878	blood:	n/a	n/a
4	BATF	chr9:140710900-140711326	GM12878	blood:	n/a	chr9:140711120-140711131
5	BATF	chr9:140710702-140711592	GM12878	blood:	n/a	chr9:140711120-140711131
6	BCL11A	chr9:140710826-140711435	GM12878	blood:	n/a	n/a
7	BCL11A	chr9:140674551-140675913	GM12878	blood:	n/a	n/a
8	BCL11A	chr9:140703488-140703846	GM12878	blood:	n/a	n/a
9	BCL3	chr9:140707638-140708059	GM12878	blood:	n/a	n/a
10	BCL3	chr9:140675450-140675734	GM12878	blood:	n/a	n/a
11	BCL3	chr9:140674914-140675145	GM12878	blood:	n/a	n/a
12	BCL3	chr9:140674295-140674898	GM12878	blood:	n/a	n/a
13	BCL3	chr9:140675789-140676170	GM12878	blood:	n/a	n/a
14	BCL3	chr9:140699190-140700049	GM12878	blood:	n/a	n/a
15	BCL3	chr9:140702187-140702477	GM12878	blood:	n/a	n/a
16	BCL3	chr9:140674364-140675145	GM12878	blood:	n/a	n/a
17	BCL3	chr9:140675353-140676090	GM12878	blood:	n/a	n/a
18	BCL3	chr9:140707704-140708126	GM12878	blood:	n/a	n/a
19	BCL3	chr9:140676233-140676492	GM12878	blood:	n/a	n/a
20	BCL3	chr9:140699230-140700056	GM12878	blood:	n/a	n/a
21	BCLAF1	chr9:140703525-140703782	GM12878	blood:	n/a	n/a
22	BCLAF1	chr9:140703419-140703881	GM12878	blood:	n/a	n/a
23	BCLAF1	chr9:140710805-140711566	GM12878	blood:	n/a	n/a
24	BHLHE40	chr9:140710980-140711476	GM12878	blood:	n/a	n/a
25	BHLHE40	chr9:140680209-140680621	HepG2	liver:	n/a	n/a
26	BHLHE40	chr9:140683842-140684270	HepG2	liver:	n/a	n/a
27	BRCA1	chr9:140680050-140680233	HepG2	liver:	n/a	n/a
28	CEBPB	chr9:140684103-140684275	HepG2	liver:	n/a	chr9:140684237-140684248
29	CEBPB	chr9:140674234-140674467	HepG2	liver:	n/a	chr9:140674358-140674371
30	CEBPB	chr9:140674267-140674478	A549	lung:	n/a	chr9:140674358-140674371
31	CEBPB	chr9:140681002-140681220	IMR90	lung:	n/a	n/a
32	CEBPB	chr9:140710730-140711472	GM12878	blood:	n/a	n/a
33	CEBPB	chr9:140674203-140674497	IMR90	lung:	n/a	chr9:140674358-140674371
34	CEBPB	chr9:140684121-140684398	HepG2	liver:	n/a	chr9:140684237-140684248
35	CEBPB	chr9:140680061-140680321	HepG2	liver:	n/a	chr9:140680148-140680159
36	CHD2	chr9:140711231-140711386	GM12878	blood:	n/a	n/a
37	CHD2	chr9:140699464-140699664	GM12878	blood:	n/a	n/a
38	CREB1	chr9:140710882-140711564	GM12878	blood:	n/a	n/a
39	CTCF	chr9:140675850-140675909	GM13976	blood:	n/a	n/a
40	CTCF	chr9:140673071-140673077	GM19240	blood:	n/a	n/a
41	CTCF	chr9:140711464-140711581	GM13977	blood:	n/a	n/a
42	CTCF	chr9:140680240-140680390	HepG2	liver:	n/a	n/a
43	CTCF	chr9:140680200-140680350	HepG2	liver:	n/a	n/a
44	CTCF	chr9:140673078-140673117	GM19240	blood:	n/a	n/a
45	CTCF	chr9:140680240-140680390	HCPEpiC	choroid plexus:	n/a	n/a
46	CTCF	chr9:140680320-140680470	GM12872	blood:	n/a	n/a
47	CTCF	chr9:140680140-140680290	HPF	lung:	n/a	n/a
48	CTCF	chr9:140680253-140680312	MCF-7	breast:	n/a	n/a
49	CTCF	chr9:140711501-140711544	GM12891	blood:	n/a	n/a
50	CTCF	chr9:140673018-140673093	GM12891	blood:	n/a	chr9:140673054-140673075

(count:1653 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:140683797-140683847	T-47D	breast:	n/a
2	chr9:140683527-140683577	AG04450	lung:	fetal
3	chr9:140676141-140676191	CMK	blood:	n/a
4	chr9:140681131-140681181	PrEC	prostate:	n/a
5	chr9:140675616-140675666	ovcar-3	ovarian:	n/a
6	chr9:140703637-140703687	K562	blood:	n/a
7	chr9:140683797-140683847	T-47D	breast:	n/a
8	chr9:140683527-140683577	AG04450	lung:	fetal
9	chr9:140676141-140676191	CMK	blood:	n/a
10	chr9:140681131-140681181	PrEC	prostate:	n/a
11	chr9:140675616-140675666	ovcar-3	ovarian:	n/a
12	chr9:140703637-140703687	K562	blood:	n/a
13	chr9:140703588-140703638	ProgFib	skin:	n/a
14	chr9:140707378-140707428	HEK293	kidney:	embryo
15	chr9:140673936-140673986	Caco-2	colon:	n/a
16	chr9:140684842-140684892	Hela-S3	cervix:	n/a
17	chr9:140683212-140683262	Hela-S3	cervix:	n/a
18	chr9:140707378-140707428	HL-60	blood:	n/a
19	chr9:140673936-140673986	SKMC	muscle:	n/a
20	chr9:140680393-140680443	MCF-7	breast:	n/a
21	chr9:140676141-140676191	HEK293	kidney:	embryo
22	chr9:140687144-140687194	HPAEpiC	pulmonary alveolar:	n/a
23	chr9:140676141-140676191	HepG2	liver:	n/a
24	chr9:140704763-140704813	GM06990	blood:	n/a
25	chr9:140681206-140681256	MCF-7	breast:	n/a
26	chr9:140676853-140676903	SK-N-SH_RA	brain:	n/a
27	chr9:140709558-140709608	HEK293	kidney:	embryo
28	chr9:140709558-140709608	A549	lung:	n/a
29	chr9:140683797-140683847	AG09309	skin:	n/a
30	chr9:140704398-140704448	GM12892	blood:	n/a
31	chr9:140707378-140707428	MCF-7	breast:	n/a
32	chr9:140684842-140684892	AG09319	gingival:	n/a
33	chr9:140704763-140704813	HRCEpiC	kidney:	n/a
34	chr9:140681206-140681256	AG04449	skin:	fetal
35	chr9:140681206-140681256	U87	brain:	n/a
36	chr9:140711975-140712025	RPTEC	kidney:	n/a
37	chr9:140684842-140684892	HPAEpiC	pulmonary alveolar:	n/a
38	chr9:140681206-140681256	HMEC	breast:	n/a
39	chr9:140711975-140712025	HRE	kidney:	n/a
40	chr9:140703637-140703687	HNPCEpiC	eye:	n/a
41	chr9:140683797-140683847	GM12891	blood:	n/a
42	chr9:140708214-140708264	K562	blood:	n/a
43	chr9:140683212-140683262	PrEC	prostate:	n/a
44	chr9:140676141-140676191	AG09319	gingival:	n/a
45	chr9:140705990-140706040	AG09319	gingival:	n/a
46	chr9:140675929-140675979	AoSMC	blood vessel:	n/a
47	chr9:140711975-140712025	IMR90	lung:	fetal
48	chr9:140707378-140707428	NHDF-neo	bronchial:	n/a
49	chr9:140681131-140681181	HCPEpiC	choroid plexus:	n/a
50	chr9:140676853-140676903	K562	blood:	n/a

(count:18 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:140706148..140709058-chr9:140712432..140716292,4	K562	blood:
2	chr9:140692420..140694081-chr9:140698871..140701591,2	K562	blood:
3	chr9:140700980..140705198-chr9:140707876..140710677,3	K562	blood:
4	chr9:140701752..140704462-chr9:140707799..140711263,3	MCF-7	breast:
5	chr9:140675774..140679711-chr9:140680099..140683198,4	K562	blood:
6	chr9:140692420..140694081-chr9:140698871..140701591,2	K562	blood:
7	chr9:140672962..140675618-chr9:140678748..140680768,2	K562	blood:
8	chr9:140679440..140682132-chr9:140702994..140705523,2	K562	blood:
9	chr9:140667022..140668743-chr9:140670497..140672972,3	MCF-7	breast:
10	chr9:140689938..140692282-chr9:140694934..140697761,2	MCF-7	breast:
11	chr9:140689938..140692282-chr9:140694934..140697761,2	MCF-7	breast:
12	chr9:140699377..140703481-chr9:140712801..140716368,4	K562	blood:
13	chr9:140672962..140675618-chr9:140678748..140680768,2	K562	blood:
14	chr9:140706148..140707731-chr9:140712808..140715644,2	K562	blood:
15	chr9:140700744..140703518-chr9:140712352..140715179,2	K562	blood:
16	chr9:140679440..140682132-chr9:140702994..140705523,2	K562	blood:
17	chr9:140700744..140703518-chr9:140712352..140715179,2	K562	blood:
18	chr9:140705835..140707524-chr9:140709188..140711003,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AL772363.1-5	chr9:140682117-140683139	NONHSAT135752
2	lnc-AL772363.1-4	chr9:140703295-140703875	NONHSAT135753

No data

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

Extended variants
information (count: 2086 )
Associated
traits (count: 20 )

Variant overlapped rSNPs/rCNVs (count:2086 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs398124404	chr9:140672501-140672502	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs369947749	chr9:140672536-140672537	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs371890129	chr9:140672538-140672539	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs369778034	chr9:140672545-140672546	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs548859248	chr9:140672551-140672552	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs116443577	chr9:140672555-140672556	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs373228590	chr9:140672564-140672565	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs376694474	chr9:140672565-140672566	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs145281465	chr9:140672573-140672574	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs569904009	chr9:140672580-140672581	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs537778821	chr9:140672622-140672623	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs557705669	chr9:140672635-140672636	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs371267558	chr9:140672673-140672674	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs574358087	chr9:140672675-140672676	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs112598970	chr9:140672685-140672686	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs536838258	chr9:140672694-140672695	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs553248550	chr9:140672700-140672701	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs572143747	chr9:140672701-140672702	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs74772676	chr9:140672750-140672751	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs186146931	chr9:140672773-140672774	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs149153150	chr9:140672777-140672778	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs542978953	chr9:140672807-140672808	Strong transcription ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs570554390	chr9:140672813-140672814	Strong transcription ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs563245170	chr9:140672821-140672822	Strong transcription ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs113852229	chr9:140672832-140672833	Strong transcription ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs190021664	chr9:140672851-140672852	Strong transcription ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs539575941	chr9:140672859-140672860	Strong transcription ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs559281195	chr9:140672875-140672876	Strong transcription ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs143244462	chr9:140672881-140672882	Strong transcription ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs566139510	chr9:140672932-140672933	Strong transcription ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs551571125	chr9:140672991-140672992	Strong transcription ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs113631442	chr9:140673034-140673035	Strong transcription ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs181612369	chr9:140673060-140673061	Strong transcription ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs76317412	chr9:140673075-140673076	Strong transcription ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs550943905	chr9:140673093-140673094	Strong transcription ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs567967158	chr9:140673163-140673164	Strong transcription ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs536533967	chr9:140673207-140673208	Strong transcription ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs186738480	chr9:140673241-140673242	Strong transcription ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs7857087	chr9:140673249-140673250	Strong transcription ZNF genes & repeats Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs535466441	chr9:140673269-140673270	Strong transcription ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs534749553	chr9:140673347-140673348	Strong transcription ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs75852548	chr9:140673416-140673417	Strong transcription ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs577289633	chr9:140673422-140673423	Strong transcription ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs555380018	chr9:140673448-140673449	Strong transcription ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs543023788	chr9:140673455-140673456	Strong transcription ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs562935526	chr9:140673503-140673504	Strong transcription ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs74889384	chr9:140673554-140673555	Strong transcription ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs542537796	chr9:140673556-140673557	Strong transcription ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs191581537	chr9:140673557-140673558	Strong transcription ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs182609720	chr9:140673613-140673614	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	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:1377 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:140640200-140674800	Strong transcription	HUES48 Cell Line	embryonic stem cell
2	chr9:140649800-140712400	Weak transcription	Psoas Muscle	Psoas
3	chr9:140650000-140679200	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
4	chr9:140650200-140678800	Strong transcription	Primary hematopoietic stem cells short term culture	blood
5	chr9:140650200-140682600	Strong transcription	Monocytes-CD14+_RO01746	blood
6	chr9:140650200-140700000	Strong transcription	Primary T cells from cord blood	blood
7	chr9:140650400-140673400	Weak transcription	Fetal Brain Male	brain
8	chr9:140652000-140673400	Weak transcription	Fetal Heart	heart
9	chr9:140652200-140676600	Weak transcription	Pancreatic Islets	Pancreatic Islet
10	chr9:140657400-140673000	Strong transcription	A549	lung
11	chr9:140657400-140674400	Strong transcription	Fetal Thymus	thymus
12	chr9:140657400-140677800	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr9:140658200-140674800	Strong transcription	Primary B cells from peripheral blood	blood
14	chr9:140659000-140683600	Strong transcription	Liver	Liver
15	chr9:140663800-140674400	Strong transcription	Primary T cells fromperipheralblood	blood
16	chr9:140663800-140674800	Strong transcription	Primary monocytes fromperipheralblood	blood
17	chr9:140663800-140674800	Strong transcription	Primary T helper cells fromperipheralblood	blood
18	chr9:140663800-140680400	Strong transcription	Adipose Nuclei	Adipose
19	chr9:140663800-140682000	Strong transcription	Rectal Mucosa Donor 29	rectum
20	chr9:140663800-140683000	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
21	chr9:140664000-140674600	Strong transcription	Primary T helper cells PMA-I stimulated	--
22	chr9:140664000-140674800	Strong transcription	Sigmoid Colon	Sigmoid Colon
23	chr9:140664000-140683000	Strong transcription	Stomach Smooth Muscle	stomach
24	chr9:140664200-140674400	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
25	chr9:140664200-140674800	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
26	chr9:140664200-140681000	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
27	chr9:140664200-140682600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
28	chr9:140664200-140698600	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
29	chr9:140664200-140701000	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
30	chr9:140664400-140674800	Strong transcription	Cortex derived primary cultured neurospheres	brain
31	chr9:140664600-140679000	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
32	chr9:140664600-140708000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
33	chr9:140664800-140674600	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
34	chr9:140664800-140678600	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
35	chr9:140664800-140700000	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
36	chr9:140665000-140674200	Strong transcription	Rectal Smooth Muscle	rectum
37	chr9:140665000-140681600	Strong transcription	Primary hematopoietic stem cells	blood
38	chr9:140665000-140700000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
39	chr9:140665200-140674400	Strong transcription	Colonic Mucosa	Colon
40	chr9:140665200-140674400	Strong transcription	GM12878-XiMat	blood
41	chr9:140665200-140679200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
42	chr9:140665200-140702000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
43	chr9:140665400-140675000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
44	chr9:140665400-140679400	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
45	chr9:140665400-140682800	Strong transcription	Fetal Intestine Small	intestine
46	chr9:140665400-140697800	Strong transcription	Thymus	Thymus
47	chr9:140665400-140700800	Strong transcription	Fetal Stomach	stomach
48	chr9:140665600-140679800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr9:140666000-140672800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
50	chr9:140666000-140675000	Weak transcription	Fetal Kidney	kidney

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