Variant report

Variant	nsv566138
Chromosome Location	chr14:105340643-105350355
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:32)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:32 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:105349366..105351471-chr14:105398354..105401032,2	MCF-7	breast:
2	chr14:105232900..105235354-chr14:105346063..105347686,2	K562	blood:
3	chr14:105336440..105340478-chr14:105340944..105342699,3	MCF-7	breast:
4	chr14:105345637..105347359-chr14:105353237..105355891,2	MCF-7	breast:
5	chr14:105347472..105352873-chr14:105360965..105365202,8	MCF-7	breast:
6	chr14:105329866..105333084-chr14:105347618..105350775,5	MCF-7	breast:
7	chr14:105340925..105344300-chr14:105357578..105360032,4	MCF-7	breast:
8	chr14:105283173..105285721-chr14:105343365..105345271,2	K562	blood:
9	chr14:105341650..105345212-chr14:105361341..105364354,4	MCF-7	breast:
10	chr14:105348429..105351330-chr14:105352853..105355749,4	MCF-7	breast:
11	chr14:105281635..105284024-chr14:105340547..105342098,2	MCF-7	breast:
12	chr14:105247569..105249557-chr14:105347096..105349716,2	K562	blood:
13	chr14:105345517..105346193-chr14:105435321..105435898,2	MCF-7	breast:
14	chr14:105279959..105283279-chr14:105346411..105348850,3	MCF-7	breast:
15	chr14:105346924..105348500-chr14:105353592..105356174,2	K562	blood:
16	chr14:105170806..105173679-chr14:105343574..105346385,2	MCF-7	breast:
17	chr14:105346758..105349135-chr14:105488164..105490065,2	MCF-7	breast:
18	chr14:105261927..105264053-chr14:105340389..105343258,2	K562	blood:
19	chr14:105311864..105313874-chr14:105340355..105342482,2	MCF-7	breast:
20	chr14:105331486..105332332-chr14:105342280..105343163,3	K562	blood:
21	chr14:105348765..105350400-chr14:105351876..105353640,2	MCF-7	breast:
22	chr14:105284603..105287527-chr14:105343615..105347092,3	MCF-7	breast:
23	chr14:105347000..105348818-chr14:105354613..105356174,2	K562	blood:
24	chr14:105219031..105220671-chr14:105346376..105348521,2	MCF-7	breast:
25	chr14:105337863..105340802-chr14:105451441..105454537,3	MCF-7	breast:
26	chr14:105347470..105350764-chr14:105354861..105357572,3	MCF-7	breast:
27	chr14:105349215..105352197-chr14:105846638..105849114,2	K562	blood:
28	chr14:105260881..105263647-chr14:105343476..105346245,2	K562	blood:
29	chr14:105330091..105337184-chr14:105346220..105351503,12	MCF-7	breast:
30	chr14:105343975..105346931-chr14:105350690..105354607,3	K562	blood:
31	chr14:105348832..105350459-chr14:105350760..105352328,2	K562	blood:
32	chr14:105256264..105258642-chr14:105340901..105342726,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000099814	chromatin interactions
ENSG00000142208	chromatin interactions
ENSG00000179364	chromatin interactions
ENSG00000166428	chromatin interactions
ENSG00000140104	chromatin interactions
ENSG00000184990	chromatin interactions

Extended variants
information (count: 519 )
Associated
traits (count: 105 )

Variant overlapped rSNPs/rCNVs (count:519 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2841231	chr14:105340643-105340644	Enhancers Weak transcription Genic enhancers Transcr. at gene 5' and 3' Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs564665954	chr14:105340658-105340659	Enhancers Weak transcription Genic enhancers Transcr. at gene 5' and 3' Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs530598358	chr14:105340687-105340688	Enhancers Weak transcription Genic enhancers Transcr. at gene 5' and 3' Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs550318521	chr14:105340688-105340689	Enhancers Weak transcription Genic enhancers Transcr. at gene 5' and 3' Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs560897950	chr14:105340690-105340691	Enhancers Weak transcription Genic enhancers Transcr. at gene 5' and 3' Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs529563952	chr14:105340702-105340703	Enhancers Weak transcription Genic enhancers Transcr. at gene 5' and 3' Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs145940463	chr14:105340767-105340768	Enhancers Weak transcription Genic enhancers Transcr. at gene 5' and 3' Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs559322946	chr14:105340787-105340788	Enhancers Weak transcription Genic enhancers Transcr. at gene 5' and 3' Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs377440122	chr14:105340856-105340857	Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs535264971	chr14:105340946-105340947	Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs551976755	chr14:105340993-105340994	Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs571666416	chr14:105340998-105340999	Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs537512617	chr14:105341004-105341005	Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs557081733	chr14:105341031-105341032	Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs79544488	chr14:105341050-105341051	Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs2119394	chr14:105341100-105341101	Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs2841232	chr14:105341110-105341111	Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs572781341	chr14:105341164-105341165	Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs544823254	chr14:105341212-105341213	Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs186391022	chr14:105341216-105341217	Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs3948209	chr14:105341223-105341224	Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs78369243	chr14:105341277-105341278	Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs544245303	chr14:105341294-105341295	Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs560817727	chr14:105341317-105341318	Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs529734290	chr14:105341362-105341363	Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs369440970	chr14:105341414-105341415	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs546601581	chr14:105341458-105341459	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs560111829	chr14:105341519-105341520	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs79429736	chr14:105341558-105341559	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs552013408	chr14:105341585-105341586	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs571766421	chr14:105341646-105341647	Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs74516882	chr14:105341668-105341669	Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs190891558	chr14:105341675-105341676	Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs567640382	chr14:105341676-105341677	Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs28714532	chr14:105341691-105341692	Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs536276935	chr14:105341693-105341694	Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs182846482	chr14:105341706-105341707	Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs148547296	chr14:105341801-105341802	Weak transcription Enhancers Genic enhancers ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs186514251	chr14:105341851-105341852	Weak transcription Enhancers Genic enhancers ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs191467588	chr14:105341866-105341867	Weak transcription Enhancers Genic enhancers ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs376905382	chr14:105341877-105341878	Weak transcription Enhancers Genic enhancers ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs182381269	chr14:105341896-105341897	Weak transcription Enhancers Genic enhancers ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs367960100	chr14:105341897-105341898	Weak transcription Enhancers Genic enhancers ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs57234754	chr14:105341958-105341959	Weak transcription Enhancers Genic enhancers ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs142894522	chr14:105341963-105341964	Weak transcription Enhancers Genic enhancers ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs187462889	chr14:105341968-105341969	Weak transcription Enhancers Genic enhancers ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs114714206	chr14:105341991-105341992	Weak transcription Enhancers Genic enhancers ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs560151299	chr14:105342112-105342113	Enhancers Weak transcription Genic enhancers Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs528798255	chr14:105342164-105342165	Enhancers Weak transcription Genic enhancers Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs545762852	chr14:105342229-105342230	Enhancers Weak transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:105)

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
Chronic lymphocytic leukemia	21546498	CNVD
cataract	16735990	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
small cell lung cancer	20016488	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
Urothelial carcinoma	21177765	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
Breast cancer	21364760	CNVD
small cell lung cancer	17426248	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Schizophrenia	20967226	CNVD
Non-syndromic sensorineural hearing loss	19587683	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

Chromatin state (count:418 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:105333200-105342400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr14:105333200-105344200	Weak transcription	Aorta	Aorta
3	chr14:105333200-105346600	Weak transcription	Brain Angular Gyrus	brain
4	chr14:105333200-105346800	Weak transcription	Brain Substantia Nigra	brain
5	chr14:105333200-105346800	Weak transcription	A549	lung
6	chr14:105333200-105347200	Weak transcription	Left Ventricle	heart
7	chr14:105333400-105344400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
8	chr14:105333400-105344400	Weak transcription	Cortex derived primary cultured neurospheres	brain
9	chr14:105333400-105344600	Weak transcription	H9 Cell Line	embryonic stem cell
10	chr14:105333400-105344800	Weak transcription	Brain Hippocampus Middle	brain
11	chr14:105333400-105349200	Weak transcription	Small Intestine	intestine
12	chr14:105333600-105346600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
13	chr14:105333600-105346600	Weak transcription	Colon Smooth Muscle	Colon
14	chr14:105333800-105343400	Weak transcription	Brain Cingulate Gyrus	brain
15	chr14:105333800-105344400	Weak transcription	Duodenum Smooth Muscle	Duodenum
16	chr14:105334000-105346800	Weak transcription	Brain Anterior Caudate	brain
17	chr14:105334200-105351600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
18	chr14:105334400-105342400	Weak transcription	Hela-S3	cervix
19	chr14:105334400-105342400	Weak transcription	HepG2	liver
20	chr14:105334400-105348600	Weak transcription	Fetal Brain Male	brain
21	chr14:105336000-105342400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
22	chr14:105336200-105343600	Weak transcription	Brain Germinal Matrix	brain
23	chr14:105336200-105346600	Weak transcription	Rectal Smooth Muscle	rectum
24	chr14:105336600-105344200	Weak transcription	Sigmoid Colon	Sigmoid Colon
25	chr14:105337000-105342400	Enhancers	Liver	Liver
26	chr14:105337800-105341600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
27	chr14:105338000-105342400	Enhancers	HMEC	breast
28	chr14:105338200-105341400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
29	chr14:105338200-105342600	Enhancers	Breast Myoepithelial Primary Cells	Breast
30	chr14:105338400-105341400	Enhancers	HSMMtube	muscle
31	chr14:105338400-105343000	Weak transcription	Fetal Brain Female	brain
32	chr14:105338600-105340800	Enhancers	ES-I3 Cell Line	embryonic stem cell
33	chr14:105338600-105340800	Enhancers	Stomach Mucosa	stomach
34	chr14:105338600-105342400	Enhancers	Esophagus	oesophagus
35	chr14:105338800-105341800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
36	chr14:105338800-105344400	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
37	chr14:105339000-105340800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
38	chr14:105339000-105343200	Weak transcription	Colonic Mucosa	Colon
39	chr14:105339000-105343600	Weak transcription	Right Ventricle	heart
40	chr14:105339000-105343800	Weak transcription	Brain Inferior Temporal Lobe	brain
41	chr14:105339200-105341400	Enhancers	Gastric	stomach
42	chr14:105339200-105341600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
43	chr14:105339200-105341600	Enhancers	NHEK	skin
44	chr14:105339200-105342200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
45	chr14:105339200-105343400	Weak transcription	Duodenum Mucosa	Duodenum
46	chr14:105339400-105341800	Weak transcription	Fetal Intestine Large	intestine
47	chr14:105339400-105343200	Weak transcription	Rectal Mucosa Donor 29	rectum
48	chr14:105339400-105343800	Weak transcription	Lung	lung
49	chr14:105339400-105344600	Weak transcription	Rectal Mucosa Donor 31	rectum
50	chr14:105339400-105344800	Weak transcription	Osteobl	bone

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