Variant report

Variant	esv3389842
Chromosome Location	chr18:43576604-43578902
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	ATF1	chr18:43578215-43578534	K562	blood:	n/a	n/a
2	CCNT2	chr18:43578235-43578585	K562	blood:	n/a	n/a
3	CEBPB	chr18:43578317-43578516	K562	blood:	n/a	n/a
4	EBF1	chr18:43577977-43578104	GM12878	blood:	n/a	n/a
5	EBF1	chr18:43577717-43578123	GM12878	blood:	n/a	n/a
6	ELF1	chr18:43578360-43578603	K562	blood:	n/a	n/a
7	ELF1	chr18:43577533-43577966	GM12878	blood:	n/a	chr18:43577697-43577706
8	EP300	chr18:43578076-43578657	K562	blood:	n/a	n/a
9	GATA1	chr18:43577969-43578553	K562	blood:	n/a	chr18:43578351-43578358 chr18:43578349-43578358 chr18:43578348-43578360 chr18:43578351-43578358 chr18:43578351-43578358 chr18:43578349-43578359 chr18:43578052-43578068 chr18:43578055-43578064 chr18:43578349-43578358 chr18:43578055-43578065
10	GATA2	chr18:43577960-43578539	HUVEC	blood vessel:	n/a	chr18:43578351-43578358 chr18:43578349-43578358 chr18:43578348-43578360 chr18:43578351-43578358 chr18:43578348-43578362 chr18:43578351-43578358 chr18:43578349-43578359 chr18:43578052-43578068 chr18:43578055-43578064 chr18:43578349-43578358 chr18:43578055-43578065
11	GATA2	chr18:43578147-43578526	SH-SY5Y	brain:	n/a	chr18:43578351-43578358 chr18:43578349-43578358 chr18:43578348-43578360 chr18:43578351-43578358 chr18:43578348-43578362 chr18:43578351-43578358 chr18:43578349-43578359 chr18:43578349-43578358
12	HMGN3	chr18:43578199-43578435	K562	blood:	n/a	chr18:43578350-43578357
13	IRF1	chr18:43578088-43578691	K562	blood:	n/a	chr18:43578113-43578127 chr18:43578117-43578127
14	JUND	chr18:43578152-43578633	K562	blood:	n/a	n/a
15	MAZ	chr18:43578333-43578636	K562	blood:	n/a	chr18:43578432-43578443
16	MTA3	chr18:43577701-43578271	GM12878	blood:	n/a	n/a
17	MXI1	chr18:43578190-43578390	K562	blood:	n/a	n/a
18	MYC	chr18:43578283-43578597	K562	blood:	n/a	chr18:43578432-43578443
19	MYC	chr18:43578204-43578623	K562	blood:	n/a	chr18:43578432-43578443
20	NFIC	chr18:43577699-43578320	GM12878	blood:	n/a	n/a
21	POLR2A	chr18:43578210-43578447	HUVEC	blood vessel:	n/a	n/a
22	POLR2A	chr18:43578382-43578397	K562	blood:	n/a	n/a
23	POLR2A	chr18:43577669-43577846	GM12878	blood:	n/a	n/a
24	POLR2A	chr18:43577673-43577837	GM12878	blood:	n/a	n/a
25	POLR2A	chr18:43578421-43578605	K562	blood:	n/a	n/a
26	RCOR1	chr18:43577898-43578644	K562	blood:	n/a	n/a
27	RUNX3	chr18:43577788-43578573	GM12878	blood:	n/a	n/a
28	RUNX3	chr18:43577836-43578226	GM12878	blood:	n/a	n/a
29	SPI1	chr18:43577904-43578165	GM12891	blood:	n/a	n/a
30	SRF	chr18:43578363-43578557	GM12878	blood:	n/a	n/a
31	SRF	chr18:43578350-43578579	GM12878	blood:	n/a	n/a
32	STAT3	chr18:43576769-43576847	MCF10A-Er-Src	breast:	n/a	n/a
33	TAL1	chr18:43578158-43578501	K562	blood:	n/a	chr18:43578351-43578359
34	TBL1XR1	chr18:43578157-43578403	K562	blood:	n/a	n/a
35	TEAD4	chr18:43578065-43578594	K562	blood:	n/a	n/a
36	TEAD4	chr18:43578128-43578531	K562	blood:	n/a	n/a
37	USF1	chr18:43578257-43578526	K562	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr18:43577618..43580480-chr18:43580513..43583485,2	K562	blood:
2	chr18:43572012..43574368-chr18:43575627..43577632,2	K562	blood:
3	chr18:43578214..43579999-chr18:43649262..43651951,2	K562	blood:
4	chr18:43578212..43579999-chr18:43649262..43652409,3	K562	blood:
5	chr18:43578639..43580570-chr18:43582338..43584371,2	MCF-7	breast:

Variant related genes	Relation type
PSTPIP2	TF binding region
ENSG00000152229	chromatin interactions

Extended variants
information (count: 80 )
Associated
traits (count: 88 )

Variant overlapped rSNPs/rCNVs (count:80 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs550606809	chr18:43576672-43576673	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs570331912	chr18:43576734-43576735	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs80110556	chr18:43576781-43576782	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs552931858	chr18:43576782-43576783	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs368649503	chr18:43576796-43576797	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs534946849	chr18:43576806-43576807	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs547066198	chr18:43576866-43576867	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs111339528	chr18:43576869-43576870	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs535800185	chr18:43576950-43576951	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs574364118	chr18:43576952-43576953	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs186162655	chr18:43576992-43576993	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs73438235	chr18:43577092-43577093	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs575265283	chr18:43577118-43577119	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs368318440	chr18:43577153-43577154	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs559876086	chr18:43577173-43577174	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs7351000	chr18:43577189-43577190	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs374662964	chr18:43577256-43577257	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs539335280	chr18:43577282-43577283	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs548237601	chr18:43577316-43577317	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs531209329	chr18:43577330-43577331	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs557673641	chr18:43577406-43577407	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs572991505	chr18:43577443-43577444	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs138733026	chr18:43577495-43577496	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs561783561	chr18:43577541-43577542	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs10468978	chr18:43577571-43577572	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs10468979	chr18:43577582-43577583	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs562445397	chr18:43577636-43577637	Enhancers Strong transcription Weak transcription Genic enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs369221828	chr18:43577640-43577641	Enhancers Strong transcription Weak transcription Genic enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs552895265	chr18:43577675-43577676	Enhancers Strong transcription Weak transcription Genic enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs375468516	chr18:43577703-43577704	Enhancers Strong transcription Weak transcription Genic enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs138987468	chr18:43577718-43577719	Enhancers Strong transcription Weak transcription Genic enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs182087986	chr18:43577721-43577722	Enhancers Strong transcription Weak transcription Genic enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs546885905	chr18:43577752-43577753	Enhancers Strong transcription Weak transcription Genic enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs149907143	chr18:43577757-43577758	Enhancers Strong transcription Weak transcription Genic enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs568505015	chr18:43577774-43577775	Enhancers Strong transcription Weak transcription Genic enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs187834759	chr18:43577784-43577785	Enhancers Strong transcription Weak transcription Genic enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs143925823	chr18:43577787-43577788	Enhancers Strong transcription Weak transcription Genic enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs370107204	chr18:43577806-43577807	Enhancers Genic enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs374955460	chr18:43577813-43577814	Enhancers Genic enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs183799377	chr18:43577819-43577820	Enhancers Genic enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs73953953	chr18:43577828-43577829	Enhancers Genic enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs377215144	chr18:43577845-43577846	Enhancers Genic enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs374625567	chr18:43577854-43577855	Enhancers Genic enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs188809550	chr18:43577863-43577864	Enhancers Genic enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs555296307	chr18:43577864-43577865	Enhancers Genic enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs10468858	chr18:43577865-43577866	Enhancers Genic enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs544307113	chr18:43577866-43577867	Enhancers Genic enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs562612192	chr18:43577892-43577893	Enhancers Genic enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs200983376	chr18:43577906-43577907	Enhancers Genic enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs10468980	chr18:43577908-43577909	Enhancers Genic enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:88)

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
low-grade B-cell lymphoma tumor	18367492	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
Breast cancer	21364760	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Congenital anomalies of the kidney and urinary tract	18852474	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
Prostate cancer	22341455	CNVD

Chromatin state (count:145 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:43558800-43608000	Weak transcription	Pancreas	Pancrea
2	chr18:43560400-43582600	Weak transcription	Fetal Intestine Small	intestine
3	chr18:43560400-43597600	Weak transcription	Left Ventricle	heart
4	chr18:43560600-43591600	Weak transcription	Duodenum Mucosa	Duodenum
5	chr18:43561000-43576800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
6	chr18:43562400-43583200	Weak transcription	Lung	lung
7	chr18:43562600-43585600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
8	chr18:43563400-43592000	Weak transcription	Psoas Muscle	Psoas
9	chr18:43565400-43588800	Weak transcription	Skeletal Muscle Male	skeletal muscle
10	chr18:43565400-43590800	Weak transcription	Colon Smooth Muscle	Colon
11	chr18:43565600-43588800	Weak transcription	Stomach Smooth Muscle	stomach
12	chr18:43566200-43577200	Strong transcription	Monocytes-CD14+_RO01746	blood
13	chr18:43566400-43577600	Strong transcription	Primary hematopoietic stem cells short term culture	blood
14	chr18:43567800-43578400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
15	chr18:43567800-43588800	Weak transcription	NHEK	skin
16	chr18:43568000-43583200	Weak transcription	Esophagus	oesophagus
17	chr18:43568400-43578200	Weak transcription	Rectal Mucosa Donor 29	rectum
18	chr18:43568600-43596800	Weak transcription	Adipose Nuclei	Adipose
19	chr18:43568800-43588600	Weak transcription	Duodenum Smooth Muscle	Duodenum
20	chr18:43568800-43607800	Weak transcription	Rectal Smooth Muscle	rectum
21	chr18:43569200-43577000	Weak transcription	Primary T cells from cord blood	blood
22	chr18:43569400-43588800	Weak transcription	Fetal Stomach	stomach
23	chr18:43570000-43577000	Strong transcription	Primary monocytes fromperipheralblood	blood
24	chr18:43570000-43577800	Weak transcription	K562	blood
25	chr18:43570000-43579400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
26	chr18:43570000-43583000	Weak transcription	Aorta	Aorta
27	chr18:43570200-43588800	Weak transcription	Skeletal Muscle Female	skeletal muscle
28	chr18:43571400-43622000	Weak transcription	Gastric	stomach
29	chr18:43572200-43582600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
30	chr18:43573800-43576800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
31	chr18:43573800-43582000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr18:43574000-43577800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
33	chr18:43574200-43577000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
34	chr18:43574200-43577000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
35	chr18:43574200-43582000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
36	chr18:43574200-43582600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
37	chr18:43574200-43590000	Weak transcription	HMEC	breast
38	chr18:43574200-43592000	Weak transcription	NH-A	brain
39	chr18:43574200-43593200	Weak transcription	NHDF-Ad	bronchial
40	chr18:43574200-43597400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
41	chr18:43574200-43608000	Weak transcription	NHLF	lung
42	chr18:43574400-43577600	Weak transcription	HSMM	muscle
43	chr18:43574600-43608000	Weak transcription	Osteobl	bone
44	chr18:43575400-43580600	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
45	chr18:43575600-43577800	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
46	chr18:43575800-43577000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
47	chr18:43575800-43578600	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
48	chr18:43576000-43577000	Strong transcription	Liver	Liver
49	chr18:43576000-43577800	Enhancers	Primary T killer memory cells from peripheral blood	blood
50	chr18:43576000-43579800	Enhancers	Primary T killer naive cells fromperipheralblood	blood

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