Variant report

Variant	nsv1059619
Chromosome Location	chr18:45384301-45401360
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:99)
CpG islands
(count:0)
Chromatin interactive
region (count:12)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:99 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr18:45397603-45397941	HepG2	liver:	n/a	chr18:45397770-45397786
2	BACH1	chr18:45391890-45391917	K562	blood:	n/a	n/a
3	CEBPB	chr18:45390754-45391063	HepG2	liver:	n/a	n/a
4	CEBPB	chr18:45390790-45391041	A549	lung:	n/a	n/a
5	CEBPB	chr18:45390727-45391043	IMR90	lung:	n/a	n/a
6	CEBPB	chr18:45389601-45389752	A549	lung:	n/a	n/a
7	CEBPB	chr18:45397656-45397855	HepG2	liver:	n/a	chr18:45397738-45397749
8	CTCF	chr18:45397147-45397225	GM12878	blood:	n/a	n/a
9	CTCF	chr18:45397080-45397230	Hela-S3	cervix:	n/a	n/a
10	CTCF	chr18:45397000-45397150	HPAF	blood vessel:	n/a	n/a
11	CTCF	chr18:45391400-45391550	HPAF	blood vessel:	n/a	n/a
12	CTCF	chr18:45391400-45391550	HMEC	breast:	n/a	n/a
13	CTCF	chr18:45397120-45397270	HCPEpiC	choroid plexus:	n/a	n/a
14	CTCF	chr18:45391452-45391621	GM12878	blood:	n/a	n/a
15	CTCF	chr18:45397100-45397250	HRPEpiC	eye:	n/a	n/a
16	CTCF	chr18:45391431-45391563	Hela-S3	cervix:	n/a	n/a
17	CTCF	chr18:45391441-45391530	K562	blood:	n/a	n/a
18	CTCF	chr18:45391466-45391531	Medullo	brain:	n/a	n/a
19	CTCF	chr18:45397120-45397270	NHEK	skin:	n/a	n/a
20	CTCF	chr18:45397160-45397310	HMEC	breast:	n/a	n/a
21	CTCF	chr18:45397120-45397270	HEK293	kidney:	n/a	n/a
22	CTCF	chr18:45397120-45397270	HPAF	blood vessel:	n/a	n/a
23	CTCF	chr18:45397161-45397193	MCF-7	breast:	n/a	n/a
24	CTCF	chr18:45391444-45391551	MCF-7	breast:	n/a	n/a
25	CTCF	chr18:45391443-45391540	LNCaP	prostate:	n/a	n/a
26	CTCF	chr18:45399007-45399037	Spleen_OC	spleen:	n/a	n/a
27	CTCF	chr18:45391492-45391566	Lung_OC	lung:	n/a	n/a
28	CTCF	chr18:45391448-45391521	Pancreas_OC	pancreas:	n/a	n/a
29	CTCF	chr18:45395363-45395424	Lung_OC	lung:	n/a	n/a
30	CTCF	chr18:45397074-45397282	HUVEC	blood vessel:	n/a	n/a
31	CTCF	chr18:45391418-45391544	HepG2	liver:	n/a	n/a
32	CTCF	chr18:45397102-45397279	Hela-S3	cervix:	n/a	n/a
33	CTCF	chr18:45397866-45397900	Fibrobl	skin:	n/a	n/a
34	CTCF	chr18:45397176-45397227	Medullo	brain:	n/a	n/a
35	CTCF	chr18:45397097-45397248	GM12878	blood:	n/a	n/a
36	CTCF	chr18:45391482-45391517	LNCaP	prostate:	n/a	n/a
37	CTCF	chr18:45397147-45397238	K562	blood:	n/a	n/a
38	CTCF	chr18:45391380-45391530	HCPEpiC	choroid plexus:	n/a	n/a
39	CUX1	chr18:45400694-45400830	GM12878	blood:	n/a	n/a
40	E2F4	chr18:45398184-45398481	MCF10A-Er-Src	breast:	n/a	n/a
41	EP300	chr18:45397686-45397879	HepG2	liver:	n/a	chr18:45397739-45397753
42	FOS	chr18:45396995-45397355	MCF10A-Er-Src	breast:	n/a	n/a
43	FOS	chr18:45396998-45397354	MCF10A-Er-Src	breast:	n/a	n/a
44	FOS	chr18:45397028-45397328	MCF10A-Er-Src	breast:	n/a	n/a
45	FOS	chr18:45397005-45397354	MCF10A-Er-Src	breast:	n/a	n/a
46	FOS	chr18:45389501-45389813	MCF10A-Er-Src	breast:	n/a	n/a
47	FOS	chr18:45389512-45389797	MCF10A-Er-Src	breast:	n/a	n/a
48	FOXA1	chr18:45397648-45397964	HepG2	liver:	n/a	n/a
49	FOXA1	chr18:45397617-45398018	HepG2	liver:	n/a	n/a
50	FOXA1	chr18:45397588-45397935	HepG2	liver:	n/a	n/a

No data

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr18:45388105..45390269-chr18:45393560..45395389,2	K562	blood:
2	chr18:45379137..45382377-chr18:45391896..45394821,3	K562	blood:
3	chr18:45388105..45390269-chr18:45393560..45395389,2	K562	blood:
4	chr18:45391818..45394321-chr18:45399787..45402085,2	MCF-7	breast:
5	chr18:45400689..45404562-chr18:45404621..45407103,3	K562	blood:
6	chr18:45390223..45391741-chr18:45457289..45459666,2	MCF-7	breast:
7	chr18:45396878..45399642-chr18:45401844..45403752,2	MCF-7	breast:
8	chr18:45393055..45395642-chr18:45402481..45404020,2	MCF-7	breast:
9	chr18:45401120..45404562-chr18:45404621..45407593,3	K562	blood:
10	chr16:2732028..2732807-chr18:45399145..45399845,2	Hela-S3	cervix:
11	chr18:45391818..45394321-chr18:45399787..45402085,2	MCF-7	breast:
12	chr17:57916192..57918375-chr18:45387752..45390655,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZBTB7C-5	chr18:45396844-45396935	NONHSAT059175

No data

Variant related genes	Relation type
ENSG00000267541	TF binding region
ENSG00000267541	chromatin interactions
ENSG00000167977	chromatin interactions
ENSG00000175387	chromatin interactions

Extended variants
information (count: 656 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:656 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs555203128	chr18:45384304-45384305	ZNF genes & repeats Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs142876063	chr18:45384308-45384309	ZNF genes & repeats Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs146565986	chr18:45384327-45384328	ZNF genes & repeats Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs557737483	chr18:45384424-45384425	ZNF genes & repeats Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs577474046	chr18:45384439-45384440	ZNF genes & repeats Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs540176177	chr18:45384477-45384478	ZNF genes & repeats Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs191434671	chr18:45384510-45384511	ZNF genes & repeats Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs140092624	chr18:45384529-45384530	ZNF genes & repeats Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs374341307	chr18:45384530-45384531	ZNF genes & repeats Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs371485158	chr18:45384625-45384626	ZNF genes & repeats Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs182708775	chr18:45384675-45384676	ZNF genes & repeats Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs374349045	chr18:45384714-45384715	ZNF genes & repeats Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs140034042	chr18:45384731-45384732	ZNF genes & repeats Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs143617234	chr18:45384772-45384773	ZNF genes & repeats Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs531856940	chr18:45384800-45384801	Weak transcription ZNF genes & repeats Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs551443347	chr18:45384847-45384848	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs565291853	chr18:45384946-45384947	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs527984692	chr18:45384953-45384954	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs146781696	chr18:45385006-45385007	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs567841783	chr18:45385054-45385055	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs75805551	chr18:45385095-45385096	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs140450379	chr18:45385105-45385106	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs112308707	chr18:45385158-45385159	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs537954406	chr18:45385162-45385163	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs372429035	chr18:45385176-45385177	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs557321973	chr18:45385252-45385253	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs79895223	chr18:45385259-45385260	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs118152293	chr18:45385308-45385309	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs533815192	chr18:45385340-45385341	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs553685897	chr18:45385363-45385364	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs573897219	chr18:45385373-45385374	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs187346940	chr18:45385404-45385405	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs562708590	chr18:45385423-45385424	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs192245506	chr18:45385443-45385444	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs150375997	chr18:45385448-45385449	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs553863892	chr18:45385491-45385492	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs527719264	chr18:45385528-45385529	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs145003600	chr18:45385541-45385542	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs561536219	chr18:45385543-45385544	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs368251252	chr18:45385550-45385551	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs530423638	chr18:45385566-45385567	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs376718579	chr18:45385615-45385616	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs72912372	chr18:45385644-45385645	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs565598367	chr18:45385646-45385647	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs570270869	chr18:45385671-45385672	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs189136693	chr18:45385674-45385675	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs531094194	chr18:45385689-45385690	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs573951585	chr18:45385691-45385692	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs570896211	chr18:45385736-45385737	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs533502588	chr18:45385772-45385773	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:87)

Disease	PMID	Source
Follicular lymphoma	20505157	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	18923191	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Medulloblastoma	21979893	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Trisomy 18 syndrome	17576883	CNVD
lymphocytic leukemia	21291569	CNVD
Barrett''s syndrome	19417022	CNVD
Ewing''s sarcoma	17952124	CNVD
Multiple myeloma	17550852	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Melanoma	18172304	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
18q deletion syndrome	19533772	CNVD
Acute myeloid leukemia	16864856	CNVD
Colorectal cancer	21102417	CNVD
Colorectal cancer	20709793	CNVD
Pancreatic cancer	21811562	CNVD
Basal cell lymphoma	21115979	CNVD
Mucosa-associated lymphoid tissue lymphomas	21459788	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Oligodendroglial tumors	17285580	CNVD
colon cancer	17210682	CNVD
Breast cancer	21785460	CNVD
Prostate cancer	16573809	CNVD
Autism	16446308	CNVD
Colorectal cancer	19359472	CNVD
Colorectal cancer	16272173	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	18056178	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Cancer	16751803	CNVD
Metanephric adenoma	20802469	CNVD
small cell lung cancer	20016488	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Colorectal cancer	21297112	CNVD
Breast cancer	17603634	CNVD
Thyroid cancer	19087340	CNVD
Urothelial carcinoma	21177765	CNVD
Oral cancer	21386901	CNVD
Colorectal cancer	19150955	CNVD
Acute myeloid leukemia	21251322	CNVD
Colorectal cancer	16912164	CNVD
Lung cancer	18438408	CNVD
Seminomas	18059402	CNVD
Breast cancer	16272173	CNVD
Breast cancer	17133270	CNVD
prenatal diagnosis	22389664	CNVD
Medulloblastoma	16783165	CNVD
Neuroblastoma	21508638	CNVD
Myelofibrosis	22110671	CNVD
Multiple myeloma	16461302	CNVD
Chronic lymphocytic leukemia	21049055	CNVD
Breast cancer	16397240	CNVD
Non-small cell lung cancer	21829676	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Pilomyxoid astrocytoma	17436254	CNVD
Mental retardation	21062444	CNVD
Cancer	21183584	CNVD
Burkitt''s lymphoma	18698080	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Cancer	17160897	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Gastric cancer	16891809	CNVD
Idiopathic thrombocytopenic purpura	19566914	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16774939	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Asthma	20841430	CNVD
Prostate cancer	22341455	CNVD

Chromatin state (count:721 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:45345400-45400200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
2	chr18:45366200-45390000	Weak transcription	Colonic Mucosa	Colon
3	chr18:45366600-45408200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
4	chr18:45369800-45386400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr18:45372200-45386200	Weak transcription	H9 Cell Line	embryonic stem cell
6	chr18:45372200-45396000	Weak transcription	NHLF	lung
7	chr18:45380600-45386800	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr18:45381200-45386800	ZNF genes & repeats	Fetal Lung	lung
9	chr18:45381200-45387000	ZNF genes & repeats	Primary hematopoietic stem cells	blood
10	chr18:45381400-45385800	ZNF genes & repeats	Primary B cells from peripheral blood	blood
11	chr18:45381400-45385800	ZNF genes & repeats	Primary T helper cells fromperipheralblood	blood
12	chr18:45381600-45384600	ZNF genes & repeats	Primary Natural Killer cells fromperipheralblood	blood
13	chr18:45381600-45386000	ZNF genes & repeats	Primary T cells fromperipheralblood	blood
14	chr18:45381600-45386600	ZNF genes & repeats	Primary T regulatory cells fromperipheralblood	blood
15	chr18:45381800-45384400	ZNF genes & repeats	Primary monocytes fromperipheralblood	blood
16	chr18:45381800-45385400	ZNF genes & repeats	Primary T killer naive cells fromperipheralblood	blood
17	chr18:45381800-45385600	ZNF genes & repeats	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
18	chr18:45381800-45385800	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr18:45381800-45385800	ZNF genes & repeats	Ganglion Eminence derived primary cultured neurospheres	brain
20	chr18:45381800-45386600	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr18:45381800-45387800	ZNF genes & repeats	Dnd41	blood
22	chr18:45382000-45384400	ZNF genes & repeats	Fetal Adrenal Gland	Adrenal Gland
23	chr18:45382200-45387000	ZNF genes & repeats	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
24	chr18:45382200-45420400	Weak transcription	Right Ventricle	heart
25	chr18:45382400-45386200	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr18:45382400-45386400	ZNF genes & repeats	Monocytes-CD14+_RO01746	blood
27	chr18:45382400-45387600	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
28	chr18:45382600-45389600	Weak transcription	Placenta Amnion	Placenta Amnion
29	chr18:45382800-45384600	Weak transcription	Brain Substantia Nigra	brain
30	chr18:45383000-45389600	Weak transcription	Fetal Heart	heart
31	chr18:45383000-45396600	Strong transcription	Hela-S3	cervix
32	chr18:45383400-45385600	ZNF genes & repeats	NHDF-Ad	bronchial
33	chr18:45383400-45386400	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
34	chr18:45383600-45384400	ZNF genes & repeats	Primary T helper memory cells from peripheral blood 2	blood
35	chr18:45383600-45384400	ZNF genes & repeats	Primary T helper naive cells from peripheral blood	blood
36	chr18:45383600-45384400	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
37	chr18:45383600-45384400	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
38	chr18:45383600-45384800	ZNF genes & repeats	Colon Smooth Muscle	Colon
39	chr18:45383600-45385400	ZNF genes & repeats	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
40	chr18:45383600-45385800	ZNF genes & repeats	Primary neutrophils fromperipheralblood	blood
41	chr18:45383600-45385800	ZNF genes & repeats	Primary T helper cells PMA-I stimulated	--
42	chr18:45383600-45386600	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
43	chr18:45383600-45387000	ZNF genes & repeats	iPS-18 Cell Line	embryonic stem cell
44	chr18:45383600-45392400	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
45	chr18:45383800-45384400	ZNF genes & repeats	Fetal Thymus	thymus
46	chr18:45383800-45384600	ZNF genes & repeats	Primary T cells effector/memory enriched fromperipheralblood	blood
47	chr18:45383800-45384600	ZNF genes & repeats	Fetal Muscle Leg	muscle
48	chr18:45383800-45385000	ZNF genes & repeats	Pancreatic Islets	Pancreatic Islet
49	chr18:45383800-45385000	ZNF genes & repeats	Rectal Mucosa Donor 29	rectum
50	chr18:45383800-45385600	ZNF genes & repeats	Primary T helper naive cells fromperipheralblood	blood

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