Variant report

Variant	nsv827085
Chromosome Location	chr14:105688720-105692596
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:19)
CpG islands
(count:244)
Chromatin interactive
region (count:3)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:19 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr14:105690606-105690726	Hela-S3	cervix:	n/a	n/a
2	CTCF	chr14:105689765-105689825	GM19239	blood:	n/a	n/a
3	CTCF	chr14:105689760-105689762	GM19239	blood:	n/a	n/a
4	FOS	chr14:105689658-105689930	MCF10A-Er-Src	breast:	n/a	n/a
5	FOS	chr14:105689677-105689920	MCF10A-Er-Src	breast:	n/a	n/a
6	FOS	chr14:105689667-105689886	MCF10A-Er-Src	breast:	n/a	n/a
7	FOS	chr14:105689773-105689856	MCF10A-Er-Src	breast:	n/a	n/a
8	GATA3	chr14:105688491-105688761	SH-SY5Y	brain:	n/a	n/a
9	MAFK	chr14:105692398-105692686	HepG2	liver:	n/a	chr14:105692523-105692537 chr14:105692525-105692536 chr14:105692524-105692535 chr14:105692520-105692535 chr14:105692525-105692536
10	MAFK	chr14:105692449-105692621	HepG2	liver:	n/a	chr14:105692523-105692537 chr14:105692525-105692536 chr14:105692524-105692535 chr14:105692520-105692535 chr14:105692525-105692536
11	MAX	chr14:105689521-105690041	ECC-1	luminal epithelium:	n/a	n/a
12	MAX	chr14:105689538-105690004	ECC-1	luminal epithelium:	n/a	n/a
13	PAX5	chr14:105689597-105689944	GM12891	blood:	n/a	n/a
14	PAX5	chr14:105689538-105689960	GM12878	blood:	n/a	n/a
15	PAX5	chr14:105689656-105689827	GM12878	blood:	n/a	n/a
16	PAX5	chr14:105689532-105690088	GM12878	blood:	n/a	n/a
17	PAX5	chr14:105689531-105689974	GM12878	blood:	n/a	n/a
18	PAX5	chr14:105689702-105689959	GM12892	blood:	n/a	n/a
19	POLR2A	chr14:105691068-105691188	HepG2	liver:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:105689766-105689816	NT2-D1	testis:	n/a
2	chr14:105689749-105689799	HL-60	blood:	n/a
3	chr14:105689749-105689799	IMR90	lung:	fetal
4	chr14:105688914-105688964	SK-N-SH	brain:	n/a
5	chr14:105688914-105688964	Jurkat	blood:	n/a
6	chr14:105689244-105689294	SK-N-MC	brain:	n/a
7	chr14:105688914-105688964	BE2_C	brain:	n/a
8	chr14:105689244-105689294	AG09319	gingival:	n/a
9	chr14:105689749-105689799	HEEpiC	esophagus:	n/a
10	chr14:105689766-105689816	HRE	kidney:	n/a
11	chr14:105689244-105689294	MCF-7	breast:	n/a
12	chr14:105689749-105689799	RPTEC	kidney:	n/a
13	chr14:105688914-105688964	ovcar-3	ovarian:	n/a
14	chr14:105688914-105688964	AG10803	skin:	n/a
15	chr14:105689766-105689816	HCM	heart:	n/a
16	chr14:105689749-105689799	U87	brain:	n/a
17	chr14:105689749-105689799	SK-N-SH_RA	brain:	n/a
18	chr14:105688914-105688964	U87	brain:	n/a
19	chr14:105688914-105688964	NB4	blood:	n/a
20	chr14:105689244-105689294	AG10803	skin:	n/a
21	chr14:105689244-105689294	GM19239	blood:	n/a
22	chr14:105688914-105688964	AG09309	skin:	n/a
23	chr14:105688914-105688964	AG04450	lung:	fetal
24	chr14:105689766-105689816	SKMC	muscle:	n/a
25	chr14:105689749-105689799	SK-N-SH	brain:	n/a
26	chr14:105689749-105689799	AG09319	gingival:	n/a
27	chr14:105689749-105689799	MCF10A-Er-Src	breast:	n/a
28	chr14:105689766-105689816	Hela-S3	cervix:	n/a
29	chr14:105688914-105688964	Hela-S3	cervix:	n/a
30	chr14:105689749-105689799	NB4	blood:	n/a
31	chr14:105689766-105689816	ProgFib	skin:	n/a
32	chr14:105689749-105689799	HRPEpiC	eye:	n/a
33	chr14:105688914-105688964	GM06990	blood:	n/a
34	chr14:105689244-105689294	PANC-1	pancreas:	n/a
35	chr14:105688914-105688964	CMK	blood:	n/a
36	chr14:105688914-105688964	H1-hESC	embryonic stem cell:	embryo
37	chr14:105689244-105689294	GM06990	blood:	n/a
38	chr14:105688914-105688964	T-47D	breast:	n/a
39	chr14:105689749-105689799	HCT-116	colon:	n/a
40	chr14:105689749-105689799	ECC-1	luminal epithelium:	n/a
41	chr14:105689766-105689816	HepG2	liver:	n/a
42	chr14:105689244-105689294	ovcar-3	ovarian:	n/a
43	chr14:105689244-105689294	HCPEpiC	choroid plexus:	n/a
44	chr14:105689766-105689816	HRPEpiC	eye:	n/a
45	chr14:105689244-105689294	HRPEpiC	eye:	n/a
46	chr14:105689244-105689294	HIPEpiC	eye:	n/a
47	chr14:105689749-105689799	Caco-2	colon:	n/a
48	chr14:105689766-105689816	T-47D	breast:	n/a
49	chr14:105689244-105689294	U87	brain:	n/a
50	chr14:105689749-105689799	GM12878	blood:	n/a

(count:3 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:105686263..105689184-chr14:105690812..105692738,2	MCF-7	breast:
2	chr14:105687326..105689962-chr14:105713390..105716265,3	MCF-7	breast:
3	chr14:105690256..105694283-chr14:105711655..105716319,5	MCF-7	breast:

No data

Variant related genes	Relation type
BRF1	TF binding region
BRF1	CpG island
ENSG00000185024	chromatin interactions
ENSG00000184887	chromatin interactions

Extended variants
information (count: 194 )
Associated
traits (count: 107 )

Variant overlapped rSNPs/rCNVs (count:194 , 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	rs587628708	chr14:105688727-105688728	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs587665060	chr14:105688730-105688731	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs78581571	chr14:105688731-105688732	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs148892728	chr14:105688757-105688758	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs140681721	chr14:105688761-105688762	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs587683143	chr14:105688809-105688810	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs587767328	chr14:105688864-105688865	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs191225501	chr14:105688873-105688874	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs587723527	chr14:105688875-105688876	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs587773377	chr14:105688891-105688892	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs183909833	chr14:105688924-105688925	Weak transcription Strong transcription	CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs11429509	chr14:105688970-105688971	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs33952452	chr14:105688977-105688978	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs78538876	chr14:105688982-105688983	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs79916719	chr14:105688984-105688985	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs587725622	chr14:105688990-105688991	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs375799545	chr14:105688997-105688998	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs374024534	chr14:105689002-105689003	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs587756826	chr14:105689004-105689005	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs187234488	chr14:105689035-105689036	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs587713605	chr14:105689047-105689048	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs587596510	chr14:105689051-105689052	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs190856753	chr14:105689052-105689053	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs587710126	chr14:105689056-105689057	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs587600032	chr14:105689059-105689060	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs12100976	chr14:105689090-105689091	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
27	rs587733251	chr14:105689102-105689103	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs587625006	chr14:105689105-105689106	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs587666911	chr14:105689155-105689156	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs587742347	chr14:105689157-105689158	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs79242150	chr14:105689171-105689172	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs587643718	chr14:105689181-105689182	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs78798804	chr14:105689183-105689184	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs370425001	chr14:105689186-105689187	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs587769887	chr14:105689187-105689188	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs182733955	chr14:105689197-105689198	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs587676586	chr14:105689200-105689201	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs587763150	chr14:105689207-105689208	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs587631277	chr14:105689212-105689213	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs373829876	chr14:105689243-105689244	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs188110364	chr14:105689245-105689246	Weak transcription Strong transcription	CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs55702470	chr14:105689253-105689254	Weak transcription Strong transcription	CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs587653068	chr14:105689267-105689268	Weak transcription Strong transcription	CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs587722501	chr14:105689281-105689282	Weak transcription Strong transcription	CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs587601376	chr14:105689348-105689349	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs587677727	chr14:105689386-105689387	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs587707491	chr14:105689402-105689403	Weak transcription ZNF genes & repeats Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs587611962	chr14:105689523-105689524	Weak transcription ZNF genes & repeats Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs191636533	chr14:105689570-105689571	Weak transcription ZNF genes & repeats Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs146590539	chr14:105689594-105689595	Weak transcription ZNF genes & repeats Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:107)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
High-proliferative meningiomas	17937814	CNVD
Non-small cell lung cancer	21044232	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Medulloblastoma	21979893	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Hepatocellular carcinoma	22174799	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	17899364	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Chronic myeloid leukemia	20724749	CNVD
Wilms tumour	21544195	CNVD
Lung cancer	18438408	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Colorectal cancer	16774939	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Neuroblastoma	18923191	CNVD
Barrett''s syndrome	19417022	CNVD
cataract	16735990	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Developmental delay	21147756	CNVD
Cancer	20164920	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Biliary cancer	19435499	CNVD
Follicular lymphoma	20505157	CNVD
Acute lymphoblastic leukemia	20139093	CNVD
Hepatocellular carcinoma	16750200	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Glioblastoma multiforme	21922591	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Ovarian cancer	22174824	CNVD
Non-small cell lung cancer	18320023	CNVD
Melanoma	17363583	CNVD
Prostate cancer	18632612	CNVD
Congenital heart defect	22367666	CNVD
Developmental delay	22367666	CNVD
Genitourinary abnormalities	22367666	CNVD
Intellectual disability	22367666	CNVD
Microcephaly	22367666	CNVD
Muscularhypotonia	22367666	CNVD
Ocular coloboma	22367666	CNVD
Teratozoospermia	22367666	CNVD
Cervical cancer	21062161	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Breast cancer	21990379	CNVD
Breast cancer	16417655	CNVD
22q11 deletion syndrome	22511897	CNVD
Cancer	21129771	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Schizophrenia	21399695	CNVD
Intracranial ependymoma	16609018	CNVD
Lung adenocarcinoma	17086460	CNVD
Gastric adenocarcinoma	19115996	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
14q deletion syndrome	22511897	CNVD
Epilepsy	22083797	CNVD
Ovarian cancer	21720365	CNVD
Cancer	17440070	CNVD
Neurocytoma	17123091	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Central neurocytomas	17123091	CNVD
Acute lymphoblastic leukemia	17315016	CNVD
Lung cancer	17086460	CNVD
Mortal	21835882	CNVD
small cell lung cancer	17426248	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Schizophrenia	20967226	CNVD
early-passage human iPS cells	21368824	CNVD
Williams Syndrome	20824207	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Pancreatic cancer	17952125	CNVD
Schizophrenia	23813976	CNVD
lymphocytic leukemia	21291569	CNVD
Cancer	20164919	CNVD
small cell lung cancer	20016488	CNVD
Recurrent pregnancy loss	19789632	CNVD
Non-syndromic sensorineural hearing loss	17431168	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Breast cancer	20369283	CNVD

Chromatin state (count:230 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:105668600-105714200	Weak transcription	HUVEC	blood vessel
2	chr14:105669800-105691200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
3	chr14:105669800-105713800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
4	chr14:105671400-105697000	Weak transcription	Small Intestine	intestine
5	chr14:105671600-105689400	Weak transcription	NHEK	skin
6	chr14:105672200-105694200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr14:105672400-105713200	Weak transcription	Osteobl	bone
8	chr14:105672600-105695600	Weak transcription	HMEC	breast
9	chr14:105673400-105690000	Weak transcription	Pancreatic Islets	Pancreatic Islet
10	chr14:105673600-105713600	Weak transcription	Stomach Mucosa	stomach
11	chr14:105673800-105689800	Weak transcription	Hela-S3	cervix
12	chr14:105674000-105696000	Strong transcription	Fetal Stomach	stomach
13	chr14:105674000-105698600	Weak transcription	HUES48 Cell Line	embryonic stem cell
14	chr14:105674200-105695800	Strong transcription	Fetal Intestine Small	intestine
15	chr14:105674800-105689600	Weak transcription	K562	blood
16	chr14:105674800-105694200	Strong transcription	Cortex derived primary cultured neurospheres	brain
17	chr14:105674800-105695400	Strong transcription	Fetal Brain Female	brain
18	chr14:105674800-105696000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
19	chr14:105675200-105695800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
20	chr14:105675400-105693400	Strong transcription	Duodenum Mucosa	Duodenum
21	chr14:105675400-105693800	Strong transcription	Primary T cells from cord blood	blood
22	chr14:105675400-105694200	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
23	chr14:105675400-105694400	Strong transcription	Brain Germinal Matrix	brain
24	chr14:105675400-105695800	Strong transcription	Dnd41	blood
25	chr14:105675600-105695400	Strong transcription	Thymus	Thymus
26	chr14:105675600-105695600	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
27	chr14:105675800-105690400	Strong transcription	Primary monocytes fromperipheralblood	blood
28	chr14:105675800-105693200	Strong transcription	Sigmoid Colon	Sigmoid Colon
29	chr14:105676800-105713800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
30	chr14:105678400-105688800	Strong transcription	Aorta	Aorta
31	chr14:105678400-105690200	Strong transcription	Rectal Mucosa Donor 29	rectum
32	chr14:105679800-105714000	Weak transcription	NHDF-Ad	bronchial
33	chr14:105680600-105714000	Weak transcription	Psoas Muscle	Psoas
34	chr14:105681400-105693200	Strong transcription	Brain Anterior Caudate	brain
35	chr14:105681400-105714000	Weak transcription	HSMMtube	muscle
36	chr14:105681400-105714200	Weak transcription	HSMM	muscle
37	chr14:105681800-105693200	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
38	chr14:105682200-105695800	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
39	chr14:105682200-105696000	Strong transcription	Primary hematopoietic stem cells short term culture	blood
40	chr14:105682400-105689400	Weak transcription	Fetal Kidney	kidney
41	chr14:105682400-105689600	Weak transcription	H9 Cell Line	embryonic stem cell
42	chr14:105682400-105693400	Weak transcription	Fetal Brain Male	brain
43	chr14:105682400-105694000	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
44	chr14:105682600-105690200	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
45	chr14:105682600-105696000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
46	chr14:105682800-105689000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
47	chr14:105682800-105689400	Weak transcription	Primary hematopoietic stem cells	blood
48	chr14:105682800-105694000	Strong transcription	Fetal Intestine Large	intestine
49	chr14:105682800-105694200	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
50	chr14:105682800-105695400	Strong transcription	Primary T cells fromperipheralblood	blood

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