Variant report

Variant	esv3427513
Chromosome Location	chr17:45214500-45214749
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:194)
CpG islands
(count:0)
Chromatin interactive
region (count:2)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:194 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr17:45212762-45214888	K562	blood:	n/a	n/a
2	ATF3	chr17:45212743-45214880	K562	blood:	n/a	n/a
3	BACH1	chr17:45212712-45214898	K562	blood:	n/a	n/a
4	BCL3	chr17:45214284-45214778	GM12878	blood:	n/a	n/a
5	BDP1	chr17:45212734-45214890	K562	blood:	n/a	n/a
6	BRCA1	chr17:45212742-45214897	Hela-S3	cervix:	n/a	n/a
7	BRCA1	chr17:45212726-45214898	GM12878	blood:	n/a	n/a
8	BRF1	chr17:45212753-45214897	K562	blood:	n/a	n/a
9	BRF2	chr17:45212730-45214887	K562	blood:	n/a	n/a
10	BRF2	chr17:45212732-45214887	Hela-S3	cervix:	n/a	n/a
11	CTCF	chr17:45214560-45214710	SAEC	small airway:	n/a	n/a
12	CTCF	chr17:45214560-45214710	HL-60	blood:	n/a	n/a
13	CTCF	chr17:45214560-45214710	HRE	kidney:	n/a	n/a
14	CTCF	chr17:45214560-45214710	AG10803	skin:	n/a	n/a
15	CTCF	chr17:45214560-45214710	Caco-2	colon:	n/a	n/a
16	CTCF	chr17:45214560-45214710	K562	blood:	n/a	n/a
17	CTCF	chr17:45214560-45214710	HCFaa	heart:	n/a	n/a
18	CTCF	chr17:45214460-45214610	GM12873	blood:	n/a	n/a
19	CTCF	chr17:45214540-45214690	NB4	blood:	n/a	n/a
20	CTCF	chr17:45214560-45214710	HBMEC	blood vessel:	n/a	n/a
21	CTCF	chr17:45214540-45214690	RPTEC	kidney:	n/a	n/a
22	CTCF	chr17:45214560-45214710	AG09309	skin:	n/a	n/a
23	CTCF	chr17:45214560-45214710	GM12801	blood:	n/a	n/a
24	CTCF	chr17:45214560-45214710	Hela-S3	cervix:	n/a	n/a
25	CTCF	chr17:45214560-45214710	AG04450	lung:	n/a	n/a
26	CTCF	chr17:45214540-45214690	A549	lung:	n/a	n/a
27	CTCF	chr17:45214540-45214690	HCM	heart:	n/a	n/a
28	CTCF	chr17:45214557-45214655	ProgFib	skin:	n/a	n/a
29	CTCF	chr17:45214460-45214610	HCM	heart:	n/a	n/a
30	CTCF	chr17:45214540-45214690	GM12866	blood:	n/a	n/a
31	CTCF	chr17:45214440-45214590	GM12870	blood:	n/a	n/a
32	CTCF	chr17:45214540-45214690	HCT-116	colon:	n/a	n/a
33	CTCF	chr17:45214560-45214710	WERI-Rb-1	eye:	n/a	n/a
34	CTCF	chr17:45214560-45214710	GM12865	blood:	n/a	n/a
35	CTCF	chr17:45214540-45214690	GM12870	blood:	n/a	n/a
36	CTCF	chr17:45214540-45214690	NHDF-neo	bronchial:	n/a	n/a
37	CTCF	chr17:45214460-45214610	HCT-116	colon:	n/a	n/a
38	CTCF	chr17:45214540-45214690	NHEK	skin:	n/a	n/a
39	CTCF	chr17:45214560-45214710	HEK293	kidney:	n/a	n/a
40	CTCF	chr17:45214560-45214710	HVMF	connective:	n/a	n/a
41	CTCF	chr17:45214480-45214630	AG04450	lung:	n/a	n/a
42	CTCF	chr17:45214560-45214710	HA-sp	spinal cord:	n/a	n/a
43	CTCF	chr17:45214540-45214690	AG09319	gingival:	n/a	n/a
44	CTCF	chr17:45214440-45214590	NHDF-neo	bronchial:	n/a	n/a
45	CTCF	chr17:45214560-45214710	HMEC	breast:	n/a	n/a
46	CTCF	chr17:45214540-45214690	WI-38	lung:	n/a	n/a
47	CTCF	chr17:45214560-45214710	GM12873	blood:	n/a	n/a
48	CTCF	chr17:45214460-45214610	HAc	cerebellar:	n/a	n/a
49	CTCF	chr17:45214440-45214590	GM12867	blood:	n/a	n/a
50	CTCF	chr17:45214540-45214690	HRPEpiC	eye:	n/a	n/a

No data

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr17:45214288..45216196-chr2:133019606..133021862,2	MCF-7	breast:
2	chr17:45211653..45214560-chr17:45231641..45234372,2	MCF-7	breast:

No data

Variant related genes	Relation type
CDC27	TF binding region
ENSG00000004897	chromatin interactions
ENSG00000233786	chromatin interactions

Extended variants
information (count: 37 )
Associated
traits (count: 118 )

Variant overlapped rSNPs/rCNVs (count:37 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs80219523	chr17:45214500-45214501	ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Strong transcription Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs201385499	chr17:45214501-45214502	ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Strong transcription Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs199609959	chr17:45214510-45214511	ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Strong transcription Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs200720095	chr17:45214518-45214519	ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Strong transcription Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs74348171	chr17:45214519-45214520	ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Strong transcription Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs62075617	chr17:45214523-45214524	ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Strong transcription Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs62075618	chr17:45214527-45214528	ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Strong transcription Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs62075619	chr17:45214544-45214545	ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Strong transcription Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs77685276	chr17:45214558-45214559	ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Strong transcription Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs201009764	chr17:45214559-45214560	ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Strong transcription Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs201184967	chr17:45214564-45214565	ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Strong transcription Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs75731161	chr17:45214582-45214583	ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Strong transcription Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs79285536	chr17:45214592-45214593	ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Strong transcription Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs112627286	chr17:45214600-45214601	ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Strong transcription Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs75661039	chr17:45214604-45214605	ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs76926116	chr17:45214605-45214606	ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs79260965	chr17:45214606-45214607	ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs138264973	chr17:45214617-45214618	ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs75637741	chr17:45214623-45214624	ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs534711882	chr17:45214630-45214631	ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs11570544	chr17:45214631-45214632	ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs148087250	chr17:45214633-45214634	ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs200200993	chr17:45214636-45214637	ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs138020641	chr17:45214643-45214644	ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs111322439	chr17:45214661-45214662	ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs62075620	chr17:45214669-45214670	ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs62075621	chr17:45214673-45214674	ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs62075622	chr17:45214682-45214683	ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs11570543	chr17:45214685-45214686	ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs74390782	chr17:45214690-45214691	ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs200907637	chr17:45214698-45214699	ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs62075623	chr17:45214699-45214700	ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs201293466	chr17:45214708-45214709	ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs199588106	chr17:45214726-45214727	ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs77871715	chr17:45214729-45214730	ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs147346652	chr17:45214730-45214731	ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs536202280	chr17:45214742-45214743	ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:118)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Ovarian cancer	22174824	CNVD
Melanoma	18172304	CNVD
Moyamoya disease	22323933	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Ovarian cancer	21781307	CNVD
Colorectal cancer	21645411	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Medulloblastoma	21979893	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell lymphomas	19863542	CNVD
Cancer	16751803	CNVD
Chordoma	21602918	CNVD
Neurofibromatosis	20686819	CNVD
Peripheral nerve sheath tumors	20686819	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Neuroblastoma	18923524	CNVD
Neuroblastoma	17897457	CNVD
Neuroblastoma	17327916	CNVD
Breast cancer	21264507	CNVD
Endometrial cancer	22040021	CNVD
Neuroblastoma	21484798	CNVD
Breast cancer	22028636	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute myeloid leukemia	20724749	CNVD
Breast cancer	21858162	CNVD
lymphocytic leukemia	21291569	CNVD
Gastric cancer	17167181	CNVD
Breast cancer	19287154	CNVD
Leukemia	20874852	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Neuroblastoma	18664255	CNVD
Neuroblastoma	17533364	CNVD
Human rectal carcinomas	16397240	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Breast cancer	17457667	CNVD
Breast cancer	16951389	CNVD
Basal cell lymphoma	17053054	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	22048815	CNVD
Breast cancer	17603634	CNVD
Follicular lymphoma	20505157	CNVD
Non-small cell lung cancer	20864512	CNVD
Cancer	21183584	CNVD
Cervical cancer	21062161	CNVD
Breast cancer	20953835	CNVD
Thyroid cancer	19087340	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
TAR Syndrome	17847015	CNVD
Neuroblastoma	18923191	CNVD
Breast cancer	17850661	CNVD
Breast cancer	19261255	CNVD
Lung cancer	16773561	CNVD
Neurocytoma	17123091	CNVD
Central neurocytomas	17123091	CNVD
Basal-like breast cancer	18066063	CNVD
Breast cancer	20031965	CNVD
Colorectal cancer	19287155	CNVD
Hereditary breast	19566914	CNVD
Ovarian cancer	19047089	CNVD
Ovarian cancer	19566914	CNVD
Triple-negative breast cancer	18950515	CNVD
Breast cancer	16846527	CNVD
Bladder cancer	21909424	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Ewing''s sarcoma	18628472	CNVD
Glioblastoma multiforme	18628472	CNVD
Leukemia	18628472	CNVD
Acute myeloid leukemia	21251322	CNVD
Ewing''s sarcoma	22429812	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21509527	CNVD
Urothelial carcinoma	21177765	CNVD
Adenoid cystic carcinoma	18332873	CNVD
Breast cancer	17142309	CNVD
Breast cancer	16397240	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Myelofibrosis	22110671	CNVD
Prostate cancer	17217626	CNVD
Non-syndromic sensorineural hearing loss	21084979	CNVD
Autism	22817714	CNVD
Breast cancer	20409316	CNVD
Cancer	17160897	CNVD
Frontotemporal lobar degeneration	19640594	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Ovarian clear cell carcinoma	21343371	CNVD

Chromatin state (count:132 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:45194800-45234200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr17:45206400-45215200	Weak transcription	Brain Germinal Matrix	brain
3	chr17:45210400-45218600	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
4	chr17:45212600-45214600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
5	chr17:45212600-45214600	Weak transcription	Fetal Brain Female	brain
6	chr17:45212600-45214800	ZNF genes & repeats	Monocytes-CD14+_RO01746	blood
7	chr17:45212800-45214800	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
8	chr17:45212800-45214800	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
9	chr17:45212800-45214800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr17:45212800-45214800	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr17:45212800-45214800	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
12	chr17:45212800-45214800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr17:45212800-45214800	ZNF genes & repeats	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
14	chr17:45212800-45214800	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
15	chr17:45212800-45214800	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
16	chr17:45212800-45214800	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
17	chr17:45212800-45214800	ZNF genes & repeats	IMR90 fetal lung fibroblasts Cell Line	lung
18	chr17:45212800-45214800	ZNF genes & repeats	iPS-15b Cell Line	embryonic stem cell
19	chr17:45212800-45214800	ZNF genes & repeats	iPS-18 Cell Line	embryonic stem cell
20	chr17:45212800-45214800	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
21	chr17:45212800-45214800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr17:45212800-45214800	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr17:45212800-45214800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
24	chr17:45212800-45214800	ZNF genes & repeats	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr17:45212800-45214800	ZNF genes & repeats	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
26	chr17:45212800-45214800	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
27	chr17:45212800-45214800	ZNF genes & repeats	Primary monocytes fromperipheralblood	blood
28	chr17:45212800-45214800	ZNF genes & repeats	Primary neutrophils fromperipheralblood	blood
29	chr17:45212800-45214800	ZNF genes & repeats	Primary B cells from cord blood	blood
30	chr17:45212800-45214800	ZNF genes & repeats	Primary B cells from peripheral blood	blood
31	chr17:45212800-45214800	ZNF genes & repeats	Primary T cells fromperipheralblood	blood
32	chr17:45212800-45214800	ZNF genes & repeats	Primary hematopoietic stem cells	blood
33	chr17:45212800-45214800	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
34	chr17:45212800-45214800	ZNF genes & repeats	Primary T helper memory cells from peripheral blood 2	blood
35	chr17:45212800-45214800	ZNF genes & repeats	Primary T helper naive cells from peripheral blood	blood
36	chr17:45212800-45214800	ZNF genes & repeats	Primary T helper memory cells from peripheral blood 1	blood
37	chr17:45212800-45214800	ZNF genes & repeats	Primary T helper 17 cells PMA-I stimulated	--
38	chr17:45212800-45214800	ZNF genes & repeats	Primary T helper cells fromperipheralblood	blood
39	chr17:45212800-45214800	ZNF genes & repeats	Primary T regulatory cells fromperipheralblood	blood
40	chr17:45212800-45214800	ZNF genes & repeats	Primary T cells effector/memory enriched fromperipheralblood	blood
41	chr17:45212800-45214800	ZNF genes & repeats	Primary Natural Killer cells fromperipheralblood	blood
42	chr17:45212800-45214800	ZNF genes & repeats	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
43	chr17:45212800-45214800	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Female	--
44	chr17:45212800-45214800	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
45	chr17:45212800-45214800	ZNF genes & repeats	Muscle Satellite Cultured Cells	--
46	chr17:45212800-45214800	ZNF genes & repeats	Cortex derived primary cultured neurospheres	brain
47	chr17:45212800-45214800	ZNF genes & repeats	Ganglion Eminence derived primary cultured neurospheres	brain
48	chr17:45212800-45214800	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin03	Skin
49	chr17:45212800-45214800	ZNF genes & repeats	Primary mononuclear cells fromperipheralblood	Blood
50	chr17:45212800-45214800	ZNF genes & repeats	Adipose Nuclei	Adipose

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