Variant report

Variant	nsv971909
Chromosome Location	chr10:52344351-52348873
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr10:52345577-52345762	K562	blood:	n/a	n/a
2	ARID3A	chr10:52346350-52346636	K562	blood:	n/a	n/a
3	ATF1	chr10:52346212-52346616	K562	blood:	n/a	n/a
4	ATF3	chr10:52346288-52346657	K562	blood:	n/a	n/a
5	BACH1	chr10:52346294-52346679	K562	blood:	n/a	chr10:52346423-52346437
6	BHLHE40	chr10:52345958-52346690	K562	blood:	n/a	n/a
7	BRCA1	chr10:52346019-52346655	Hela-S3	cervix:	n/a	n/a
8	CBX3	chr10:52346002-52346614	K562	blood:	n/a	n/a
9	CBX3	chr10:52345962-52346743	HCT-116	colon:	n/a	n/a
10	CBX3	chr10:52345999-52346700	HCT-116	colon:	n/a	n/a
11	CEBPB	chr10:52346067-52346806	HCT-116	colon:	n/a	n/a
12	CEBPB	chr10:52346207-52346689	K562	blood:	n/a	n/a
13	CEBPB	chr10:52346287-52346649	IMR90	lung:	n/a	n/a
14	CEBPB	chr10:52346248-52346724	Hela-S3	cervix:	n/a	n/a
15	CEBPB	chr10:52346278-52346673	K562	blood:	n/a	n/a
16	CEBPB	chr10:52346182-52346672	A549	lung:	n/a	n/a
17	CEBPB	chr10:52346320-52346572	K562	blood:	n/a	n/a
18	CEBPB	chr10:52346020-52346901	HCT-116	colon:	n/a	n/a
19	CHD2	chr10:52346150-52346622	Hela-S3	cervix:	n/a	n/a
20	CREB1	chr10:52346049-52346729	K562	blood:	n/a	n/a
21	CREB1	chr10:52346201-52346644	K562	blood:	n/a	n/a
22	CTCF	chr10:52346314-52346516	K562	blood:	n/a	n/a
23	CTCF	chr10:52346300-52346450	GM12864	blood:	n/a	n/a
24	CUX1	chr10:52346041-52346915	K562	blood:	n/a	n/a
25	E2F6	chr10:52346149-52346460	K562	blood:	n/a	n/a
26	E2F6	chr10:52346252-52346557	K562	blood:	n/a	n/a
27	ELF1	chr10:52346256-52346651	K562	blood:	n/a	n/a
28	ELF1	chr10:52344372-52344726	K562	blood:	n/a	chr10:52344518-52344531
29	ELK1	chr10:52346135-52346140	K562	blood:	n/a	n/a
30	EP300	chr10:52346217-52346647	K562	blood:	n/a	n/a
31	EP300	chr10:52346275-52346691	Hela-S3	cervix:	n/a	n/a
32	FOS	chr10:52346269-52346616	MCF10A-Er-Src	breast:	n/a	chr10:52346425-52346434 chr10:52346424-52346435 chr10:52346426-52346435
33	FOS	chr10:52346249-52346651	MCF10A-Er-Src	breast:	n/a	chr10:52346425-52346434 chr10:52346424-52346435 chr10:52346426-52346435
34	FOS	chr10:52346266-52346642	MCF10A-Er-Src	breast:	n/a	chr10:52346425-52346434 chr10:52346424-52346435 chr10:52346426-52346435
35	FOS	chr10:52346272-52346638	MCF10A-Er-Src	breast:	n/a	chr10:52346425-52346434 chr10:52346424-52346435 chr10:52346426-52346435
36	FOS	chr10:52346191-52346619	K562	blood:	n/a	chr10:52346425-52346434 chr10:52346424-52346435 chr10:52346426-52346435
37	FOS	chr10:52346241-52346613	HUVEC	blood vessel:	n/a	chr10:52346425-52346434 chr10:52346424-52346435 chr10:52346426-52346435
38	FOSL1	chr10:52346235-52346573	K562	blood:	n/a	chr10:52346425-52346434 chr10:52346424-52346435 chr10:52346426-52346435
39	FOSL1	chr10:52346038-52346758	HCT-116	colon:	n/a	chr10:52346425-52346434 chr10:52346424-52346435 chr10:52346426-52346435
40	FOSL1	chr10:52346086-52346727	HCT-116	colon:	n/a	chr10:52346425-52346434 chr10:52346424-52346435 chr10:52346426-52346435
41	FOSL1	chr10:52346171-52346611	K562	blood:	n/a	chr10:52346425-52346434 chr10:52346424-52346435 chr10:52346426-52346435
42	FOSL2	chr10:52346194-52346611	A549	lung:	n/a	chr10:52346425-52346434 chr10:52346426-52346435
43	GATA2	chr10:52344484-52344771	SH-SY5Y	brain:	n/a	n/a
44	GATA3	chr10:52344516-52345375	MCF-7	breast:	n/a	chr10:52344894-52344903 chr10:52344896-52344906
45	GATA3	chr10:52344713-52345047	SH-SY5Y	brain:	n/a	chr10:52344894-52344903 chr10:52344896-52344906
46	GTF2F1	chr10:52345982-52346747	Hela-S3	cervix:	n/a	n/a
47	GTF2F1	chr10:52346540-52346559	H1-hESC	embryonic stem cell:	n/a	n/a
48	HCFC1	chr10:52345986-52346601	K562	blood:	n/a	n/a
49	HDAC2	chr10:52346261-52346641	K562	blood:	n/a	n/a
50	IRF1	chr10:52346011-52346708	K562	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr10:52342671..52345197-chr10:52362617..52364673,2	MCF-7	breast:
2	chr10:52346285..52348246-chr10:52382049..52384248,2	MCF-7	breast:
3	chr10:52345136..52347979-chr10:52349121..52350897,2	MCF-7	breast:
4	chr10:52287492..52289090-chr10:52346967..52349226,2	K562	blood:
5	chr10:52338053..52345279-chr10:52380666..52386211,11	MCF-7	breast:
6	chr10:52342227..52348125-chr10:52381237..52386507,8	K562	blood:
7	chr10:52346537..52348332-chr10:52378536..52380819,2	K562	blood:
8	chr10:52343887..52348125-chr10:52383719..52386062,5	K562	blood:
9	chr10:52335825..52337405-chr10:52342195..52344591,2	K562	blood:
10	chr10:52343264..52344901-chr10:52348884..52350629,3	K562	blood:
11	chr10:52341787..52346100-chr10:52382899..52385718,8	MCF-7	breast:
12	chr10:52342133..52345402-chr10:52352257..52355042,3	MCF-7	breast:
13	chr10:52346092..52348176-chr10:52375554..52378162,2	K562	blood:
14	chr10:52346124..52348507-chr10:52350618..52352666,3	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-A1CF-2	chr10:52348409-52348560	ENSG00000226561.1

Variant related genes	Relation type
RMRPP4	TF binding region
ENSG00000198964	chromatin interactions
ENSG00000238523	chromatin interactions
ENSG00000226200	chromatin interactions

Extended variants
information (count: 160 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:160 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs565255231	chr10:52344381-52344382	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs184947615	chr10:52344388-52344389	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs542236060	chr10:52344397-52344398	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs369460452	chr10:52344515-52344516	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs533628824	chr10:52344568-52344569	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs146902449	chr10:52344593-52344594	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs561515646	chr10:52344692-52344693	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs34717216	chr10:52344742-52344743	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs189640389	chr10:52344754-52344755	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs139401276	chr10:52344761-52344762	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs182297834	chr10:52344772-52344773	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs16906349	chr10:52344776-52344777	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs375002358	chr10:52344840-52344841	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs114954328	chr10:52344868-52344869	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs369300915	chr10:52344903-52344904	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs141402138	chr10:52344919-52344920	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs529400262	chr10:52344936-52344937	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs536788826	chr10:52344941-52344942	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs561974271	chr10:52344954-52344955	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs74764821	chr10:52344979-52344980	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs185311539	chr10:52344980-52344981	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs190109110	chr10:52345033-52345034	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs549456109	chr10:52345051-52345052	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs552861196	chr10:52345064-52345065	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs181358616	chr10:52345068-52345069	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs569209934	chr10:52345215-52345216	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs185288577	chr10:52345317-52345318	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs558943386	chr10:52345331-52345332	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs575547677	chr10:52345339-52345340	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs557498458	chr10:52345348-52345349	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs369247055	chr10:52345355-52345356	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs544724194	chr10:52345357-52345358	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs571300576	chr10:52345385-52345386	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs150411331	chr10:52345403-52345404	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs540802010	chr10:52345479-52345480	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs560500297	chr10:52345553-52345554	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs188204909	chr10:52345555-52345556	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs181008194	chr10:52345578-52345579	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs76714321	chr10:52345593-52345594	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs530377361	chr10:52345600-52345601	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs550268171	chr10:52345601-52345602	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs556792646	chr10:52345615-52345616	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs185055503	chr10:52345730-52345731	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs192045691	chr10:52345794-52345795	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs566532061	chr10:52345804-52345805	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs553386840	chr10:52345884-52345885	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs11006219	chr10:52345967-52345968	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs2983364	chr10:52345974-52345975	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs556226393	chr10:52345991-52345992	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs112961088	chr10:52346033-52346034	Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:59)

Disease	PMID	Source
Pancreatic endocrine tumor	17639061	CNVD
Gastric cancer	17908304	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Melanoma	18172304	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Ewing''s sarcoma	17952124	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	20724749	CNVD
Autism	22495311	CNVD
Esophageal cancer	21851588	CNVD
Prostate cancer	18632612	CNVD
Autism	18414403	CNVD
Cockayne syndrome	18421352	CNVD
Glioblastoma	16823260	CNVD
Medulloblastoma	16968546	CNVD
Neuroblastoma	17533364	CNVD
Cancer	21183584	CNVD
T-cell lymphomas	19863542	CNVD
Testicular germ cell tumor	18059402	CNVD
Squamous cell cancer	21044232	CNVD
Glioma	21971842	CNVD
Cancer	21637783	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Obesity	21956041	CNVD
Renal cell carcinoma	18765545	CNVD
Developmental delay	21948486	CNVD
Dysmorphic features	21948486	CNVD
Epilepsy	21948486	CNVD
Breast cancer	21785460	CNVD
Intellectual disability	21948486	CNVD
Intellectual disability	22045946	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	21990379	CNVD
Myelofibrosis	22110671	CNVD
Metanephric adenoma	20802469	CNVD
Autism	20841430	CNVD
Cancer	20164920	CNVD

Chromatin state (count:273 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:52322000-52348600	Weak transcription	Fetal Stomach	stomach
2	chr10:52336200-52346000	Weak transcription	Esophagus	oesophagus
3	chr10:52336200-52349000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
4	chr10:52336400-52346200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
5	chr10:52336400-52348600	Weak transcription	Lung	lung
6	chr10:52336600-52346000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr10:52336600-52346000	Weak transcription	NHEK	skin
8	chr10:52336800-52363000	Weak transcription	Rectal Smooth Muscle	rectum
9	chr10:52337000-52348000	Weak transcription	Thymus	Thymus
10	chr10:52337800-52346200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
11	chr10:52337800-52346400	Weak transcription	Spleen	Spleen
12	chr10:52337800-52347800	Weak transcription	Fetal Thymus	thymus
13	chr10:52337800-52352800	Weak transcription	Fetal Brain Male	brain
14	chr10:52338000-52345600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
15	chr10:52338000-52346000	Weak transcription	Ovary	ovary
16	chr10:52338000-52346000	Weak transcription	Placenta Amnion	Placenta Amnion
17	chr10:52338000-52346200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
18	chr10:52338000-52346200	Weak transcription	HUVEC	blood vessel
19	chr10:52338000-52356400	Weak transcription	Fetal Brain Female	brain
20	chr10:52338000-52363800	Weak transcription	Fetal Kidney	kidney
21	chr10:52338000-52367000	Weak transcription	Aorta	Aorta
22	chr10:52338200-52346200	Weak transcription	NHDF-Ad	bronchial
23	chr10:52338200-52346400	Weak transcription	Adipose Nuclei	Adipose
24	chr10:52338200-52346400	Weak transcription	Osteobl	bone
25	chr10:52338200-52347600	Weak transcription	Fetal Muscle Leg	muscle
26	chr10:52338200-52347800	Weak transcription	Skeletal Muscle Male	skeletal muscle
27	chr10:52338200-52348800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
28	chr10:52338200-52353600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
29	chr10:52338200-52353800	Weak transcription	Stomach Smooth Muscle	stomach
30	chr10:52338400-52346000	Weak transcription	Primary monocytes fromperipheralblood	blood
31	chr10:52338400-52346200	Weak transcription	Monocytes-CD14+_RO01746	blood
32	chr10:52338400-52348000	Weak transcription	Primary neutrophils fromperipheralblood	blood
33	chr10:52338600-52344400	Weak transcription	Colon Smooth Muscle	Colon
34	chr10:52338600-52347600	Weak transcription	Duodenum Smooth Muscle	Duodenum
35	chr10:52338600-52353400	Weak transcription	Brain Germinal Matrix	brain
36	chr10:52338600-52353600	Weak transcription	Cortex derived primary cultured neurospheres	brain
37	chr10:52338800-52347800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
38	chr10:52338800-52348000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
39	chr10:52339400-52344400	Weak transcription	Pancreatic Islets	Pancreatic Islet
40	chr10:52339600-52346000	Weak transcription	Placenta	Placenta
41	chr10:52340400-52346000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
42	chr10:52340400-52360200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
43	chr10:52341000-52346000	Weak transcription	Duodenum Mucosa	Duodenum
44	chr10:52341000-52346200	Weak transcription	Primary B cells from peripheral blood	blood
45	chr10:52341000-52347600	Weak transcription	Fetal Lung	lung
46	chr10:52341000-52348000	Weak transcription	Rectal Mucosa Donor 31	rectum
47	chr10:52341200-52346000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
48	chr10:52341200-52347400	Weak transcription	HepG2	liver
49	chr10:52341200-52347800	Weak transcription	HUES64 Cell Line	embryonic stem cell
50	chr10:52341200-52348800	Weak transcription	Rectal Mucosa Donor 29	rectum

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