Variant report

Variant	esv3403668
Chromosome Location	chr14:105801457-105803170
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:4)
CpG islands
(count:245)
Chromatin interactive
region (count:2)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:4 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	EGR1	chr14:105801493-105801837	H1-hESC	embryonic stem cell:	n/a	n/a
2	MAFK	chr14:105802491-105802538	HepG2	liver:	n/a	chr14:105802501-105802516 chr14:105802505-105802516
3	ZNF263	chr14:105803119-105803613	HEK293-T-REx	kidney:	n/a	n/a
4	ZNF263	chr14:105802676-105802881	HEK293-T-REx	kidney:	n/a	n/a

(count:245 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:105802735-105802785	NB4	blood:	n/a
2	chr14:105802735-105802785	NB4	blood:	n/a
3	chr14:105802735-105802785	GM19239	blood:	n/a
4	chr14:105802387-105802437	HCM	heart:	n/a
5	chr14:105802735-105802785	NHDF-neo	bronchial:	n/a
6	chr14:105802387-105802437	NB4	blood:	n/a
7	chr14:105801706-105801756	HIPEpiC	eye:	n/a
8	chr14:105802735-105802785	PANC-1	pancreas:	n/a
9	chr14:105802735-105802785	HEK293	kidney:	embryo
10	chr14:105802735-105802785	H1-hESC	embryonic stem cell:	embryo
11	chr14:105801706-105801756	AG04449	skin:	fetal
12	chr14:105802735-105802785	HRPEpiC	eye:	n/a
13	chr14:105801706-105801756	GM19239	blood:	n/a
14	chr14:105801706-105801756	HEK293	kidney:	embryo
15	chr14:105802918-105802968	BE2_C	brain:	n/a
16	chr14:105802735-105802785	AG04450	lung:	fetal
17	chr14:105802387-105802437	SKMC	muscle:	n/a
18	chr14:105802918-105802968	SK-N-SH	brain:	n/a
19	chr14:105802735-105802785	NH-A	brain:	n/a
20	chr14:105802387-105802437	ovcar-3	ovarian:	n/a
21	chr14:105802735-105802785	SAEC	small airway:	n/a
22	chr14:105802387-105802437	HNPCEpiC	eye:	n/a
23	chr14:105801706-105801756	HCPEpiC	choroid plexus:	n/a
24	chr14:105802918-105802968	A549	lung:	n/a
25	chr14:105802918-105802968	SAEC	small airway:	n/a
26	chr14:105801706-105801756	MCF10A-Er-Src	breast:	n/a
27	chr14:105801706-105801756	NT2-D1	testis:	n/a
28	chr14:105802735-105802785	MCF-7	breast:	n/a
29	chr14:105802735-105802785	IMR90	lung:	fetal
30	chr14:105802918-105802968	GM19239	blood:	n/a
31	chr14:105801706-105801756	HUVEC	blood vessel:	n/a
32	chr14:105802918-105802968	AG09319	gingival:	n/a
33	chr14:105802387-105802437	HEK293	kidney:	embryo
34	chr14:105802735-105802785	BJ	skin:	n/a
35	chr14:105801706-105801756	HCF	heart:	n/a
36	chr14:105802918-105802968	BJ	skin:	n/a
37	chr14:105802387-105802437	GM12878	blood:	n/a
38	chr14:105802735-105802785	HEEpiC	esophagus:	n/a
39	chr14:105802918-105802968	HepG2	liver:	n/a
40	chr14:105802387-105802437	Hepatocyte	liver:	n/a
41	chr14:105802735-105802785	Hepatocyte	liver:	n/a
42	chr14:105802918-105802968	RPTEC	kidney:	n/a
43	chr14:105801706-105801756	HMEC	breast:	n/a
44	chr14:105802387-105802437	GM19239	blood:	n/a
45	chr14:105802735-105802785	SK-N-SH_RA	brain:	n/a
46	chr14:105801706-105801756	GM12891	blood:	n/a
47	chr14:105802387-105802437	LNCaP	prostate:	n/a
48	chr14:105801706-105801756	Jurkat	blood:	n/a
49	chr14:105802387-105802437	Caco-2	colon:	n/a
50	chr14:105801706-105801756	HPAEpiC	pulmonary alveolar:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr14:105795359..105796925-chr14:105800577..105802391,2	K562	blood:
2	chr14:105795771..105798760-chr14:105803162..105807544,4	K562	blood:

No data

Variant related genes	Relation type
PACS2	TF binding region
PACS2	CpG island

Extended variants
information (count: 89 )
Associated
traits (count: 106 )

Variant overlapped rSNPs/rCNVs (count:89 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs188735806	chr14:105801479-105801480	Weak transcription Enhancers Genic enhancers Strong transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
2	rs587710558	chr14:105801489-105801490	Weak transcription Enhancers Genic enhancers Strong transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
3	rs73359029	chr14:105801525-105801526	Weak transcription Enhancers Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs192582418	chr14:105801556-105801557	Weak transcription Enhancers Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs587724664	chr14:105801564-105801565	Weak transcription Enhancers Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs587603590	chr14:105801600-105801601	Weak transcription Enhancers Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs370570568	chr14:105801624-105801625	Weak transcription Enhancers Genic enhancers Strong transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs587661105	chr14:105801628-105801629	Weak transcription Enhancers Genic enhancers Strong transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs73359031	chr14:105801663-105801664	Weak transcription Enhancers Genic enhancers Strong transcription Bivalent Enhancer	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs61984701	chr14:105801675-105801676	Weak transcription Enhancers Genic enhancers Strong transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs587613777	chr14:105801676-105801677	Weak transcription Enhancers Genic enhancers Strong transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs587667743	chr14:105801679-105801680	Weak transcription Enhancers Genic enhancers Strong transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs112820110	chr14:105801687-105801688	Weak transcription Enhancers Genic enhancers Strong transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs587620716	chr14:105801692-105801693	Weak transcription Enhancers Genic enhancers Strong transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs375712369	chr14:105801693-105801694	Weak transcription Enhancers Genic enhancers Strong transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs587775342	chr14:105801709-105801710	Weak transcription Enhancers Genic enhancers Strong transcription Bivalent Enhancer	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
17	rs34341621	chr14:105801723-105801724	Weak transcription Enhancers Genic enhancers Strong transcription Bivalent Enhancer	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
18	rs587641586	chr14:105801736-105801737	Weak transcription Enhancers Genic enhancers Strong transcription Bivalent Enhancer	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
19	rs587719392	chr14:105801758-105801759	Weak transcription Enhancers Genic enhancers Strong transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs587772238	chr14:105801769-105801770	Weak transcription Enhancers Genic enhancers Strong transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs587656793	chr14:105801777-105801778	Weak transcription Enhancers Genic enhancers Strong transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs587687061	chr14:105801787-105801788	Weak transcription Enhancers Genic enhancers Strong transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs587768509	chr14:105801796-105801797	Weak transcription Enhancers Genic enhancers Strong transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs587638974	chr14:105801807-105801808	Weak transcription Genic enhancers Enhancers Strong transcription Bivalent Enhancer Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs587706199	chr14:105801823-105801824	Weak transcription Genic enhancers Enhancers Strong transcription Bivalent Enhancer Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs115759684	chr14:105801853-105801854	Weak transcription Genic enhancers Enhancers Strong transcription Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs587636594	chr14:105801981-105801982	Weak transcription Genic enhancers Enhancers Strong transcription Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs587716568	chr14:105801995-105801996	Weak transcription Genic enhancers Enhancers Strong transcription Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs147938741	chr14:105802008-105802009	Weak transcription Genic enhancers Enhancers Strong transcription Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs587674109	chr14:105802037-105802038	Weak transcription Genic enhancers Enhancers Strong transcription Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs587724193	chr14:105802042-105802043	Weak transcription Genic enhancers Enhancers Strong transcription Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs373717381	chr14:105802049-105802050	Weak transcription Genic enhancers Enhancers Strong transcription Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs587686631	chr14:105802139-105802140	Weak transcription Genic enhancers Enhancers Strong transcription Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs587766713	chr14:105802159-105802160	Weak transcription Genic enhancers Enhancers Strong transcription Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs368797114	chr14:105802160-105802161	Weak transcription Genic enhancers Enhancers Strong transcription Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs587719632	chr14:105802163-105802164	Weak transcription Genic enhancers Enhancers Strong transcription Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs182709727	chr14:105802166-105802167	Weak transcription Genic enhancers Enhancers Strong transcription Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs587628902	chr14:105802170-105802171	Weak transcription Genic enhancers Enhancers Strong transcription Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs186606227	chr14:105802173-105802174	Weak transcription Genic enhancers Enhancers Strong transcription Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs587765052	chr14:105802214-105802215	Weak transcription Genic enhancers Enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs587649109	chr14:105802222-105802223	Weak transcription Genic enhancers Enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs587683921	chr14:105802254-105802255	Weak transcription Genic enhancers Enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs191396133	chr14:105802256-105802257	Weak transcription Genic enhancers Enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs587735332	chr14:105802260-105802261	Weak transcription Genic enhancers Enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs371409811	chr14:105802296-105802297	Weak transcription Genic enhancers Enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs587720238	chr14:105802315-105802316	Weak transcription Genic enhancers Enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs111922892	chr14:105802340-105802341	Weak transcription Genic enhancers Enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs587645317	chr14:105802382-105802383	Weak transcription Genic enhancers Enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs141724601	chr14:105802390-105802391	Weak transcription Genic enhancers Enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS	CpG island	1 gene(s)	Overlapped CNVs	n/a
50	rs587604042	chr14:105802398-105802399	Weak transcription Genic enhancers Enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS	CpG island	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:106)

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
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	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
Non-syndromic sensorineural hearing loss	19587683	CNVD
Breast cancer	20369283	CNVD

Chromatin state (count:140 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:105782600-105807400	Weak transcription	Primary B cells from cord blood	blood
2	chr14:105783600-105802800	Weak transcription	Fetal Intestine Large	intestine
3	chr14:105784000-105821800	Weak transcription	Rectal Mucosa Donor 29	rectum
4	chr14:105784200-105802400	Weak transcription	Dnd41	blood
5	chr14:105789200-105805600	Enhancers	Brain Anterior Caudate	brain
6	chr14:105790000-105802200	Enhancers	Brain Hippocampus Middle	brain
7	chr14:105790200-105805400	Enhancers	Brain Substantia Nigra	brain
8	chr14:105791000-105803400	Enhancers	Fetal Muscle Leg	muscle
9	chr14:105791400-105804200	Weak transcription	Rectal Smooth Muscle	rectum
10	chr14:105791800-105803600	Weak transcription	Colon Smooth Muscle	Colon
11	chr14:105792400-105804200	Weak transcription	Duodenum Smooth Muscle	Duodenum
12	chr14:105793400-105804400	Weak transcription	Fetal Lung	lung
13	chr14:105793800-105821000	Weak transcription	H9 Cell Line	embryonic stem cell
14	chr14:105794600-105801800	Enhancers	Skeletal Muscle Female	skeletal muscle
15	chr14:105797000-105806800	Weak transcription	Aorta	Aorta
16	chr14:105797000-105849200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
17	chr14:105797200-105804000	Weak transcription	Colonic Mucosa	Colon
18	chr14:105797200-105804200	Weak transcription	Monocytes-CD14+_RO01746	blood
19	chr14:105797200-105804200	Weak transcription	NHEK	skin
20	chr14:105797200-105804400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
21	chr14:105797200-105804600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
22	chr14:105797200-105806600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr14:105797200-105810600	Weak transcription	HUES6 Cell Line	embryonic stem cell
24	chr14:105797200-105820800	Weak transcription	NHLF	lung
25	chr14:105797400-105802000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
26	chr14:105797400-105802600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
27	chr14:105797400-105807000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
28	chr14:105797400-105807000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr14:105797400-105812000	Weak transcription	K562	blood
30	chr14:105797400-105821200	Weak transcription	H1 Cell Line	embryonic stem cell
31	chr14:105798000-105802200	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
32	chr14:105798200-105802400	Enhancers	Brain Inferior Temporal Lobe	brain
33	chr14:105798200-105803800	Weak transcription	Cortex derived primary cultured neurospheres	brain
34	chr14:105798200-105818400	Weak transcription	HUES48 Cell Line	embryonic stem cell
35	chr14:105798400-105802000	Enhancers	Brain Cingulate Gyrus	brain
36	chr14:105798400-105805400	Enhancers	Left Ventricle	heart
37	chr14:105798400-105805600	Enhancers	Right Ventricle	heart
38	chr14:105798400-105809400	Weak transcription	HepG2	liver
39	chr14:105798600-105803000	Enhancers	HSMMtube	muscle
40	chr14:105798600-105803200	Enhancers	Brain Angular Gyrus	brain
41	chr14:105798600-105805200	Enhancers	Pancreas	Pancrea
42	chr14:105798800-105802400	Weak transcription	Fetal Intestine Small	intestine
43	chr14:105798800-105803200	Strong transcription	Fetal Stomach	stomach
44	chr14:105798800-105803800	Weak transcription	Primary monocytes fromperipheralblood	blood
45	chr14:105798800-105803800	Weak transcription	Primary hematopoietic stem cells	blood
46	chr14:105798800-105804400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
47	chr14:105798800-105807000	Weak transcription	Primary T cells from cord blood	blood
48	chr14:105799000-105803000	Enhancers	Fetal Heart	heart
49	chr14:105799000-105806800	Weak transcription	Fetal Thymus	thymus
50	chr14:105799000-105807200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood

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