Variant report

Variant	nsv983806
Chromosome Location	chr14:24427320-24439098
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:137)
CpG islands
(count:183)
Chromatin interactive
region (count:1)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:137 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BCL11A	chr14:24435772-24436067	GM12878	blood:	n/a	chr14:24435972-24435981
2	BHLHE40	chr14:24438814-24439115	HepG2	liver:	n/a	n/a
3	CEBPD	chr14:24439025-24439361	HepG2	liver:	n/a	n/a
4	CTCF	chr14:24438642-24438741	GM13976	blood:	n/a	n/a
5	CTCF	chr14:24435876-24436058	Spleen_OC	spleen:	n/a	n/a
6	CTCF	chr14:24436009-24436038	GM13976	blood:	n/a	n/a
7	CTCF	chr14:24439058-24439117	Spleen_OC	spleen:	n/a	n/a
8	EBF1	chr14:24438510-24438735	GM12878	blood:	n/a	n/a
9	EBF1	chr14:24438433-24438849	GM12878	blood:	n/a	n/a
10	FOSL2	chr14:24436569-24437166	HepG2	liver:	n/a	n/a
11	FOSL2	chr14:24437768-24439484	HepG2	liver:	n/a	n/a
12	FOSL2	chr14:24436384-24437168	HepG2	liver:	n/a	n/a
13	FOSL2	chr14:24431329-24431556	HepG2	liver:	n/a	n/a
14	FOSL2	chr14:24435347-24435778	HepG2	liver:	n/a	n/a
15	FOSL2	chr14:24435454-24435701	HepG2	liver:	n/a	n/a
16	FOSL2	chr14:24437828-24439994	HepG2	liver:	n/a	chr14:24439561-24439570
17	FOXA1	chr14:24436443-24437096	HepG2	liver:	n/a	n/a
18	FOXA1	chr14:24438863-24439965	HepG2	liver:	n/a	n/a
19	HDAC2	chr14:24438965-24439364	HepG2	liver:	n/a	n/a
20	HEY1	chr14:24438861-24439367	K562	blood:	n/a	n/a
21	HEY1	chr14:24437997-24439432	HepG2	liver:	n/a	n/a
22	HEY1	chr14:24438852-24439174	K562	blood:	n/a	n/a
23	HEY1	chr14:24438812-24439347	HepG2	liver:	n/a	n/a
24	IRF4	chr14:24438438-24438817	GM12878	blood:	n/a	n/a
25	IRF4	chr14:24435708-24436136	GM12878	blood:	n/a	n/a
26	IRF4	chr14:24435755-24436221	GM12878	blood:	n/a	n/a
27	IRF4	chr14:24438420-24438713	GM12878	blood:	n/a	n/a
28	JUND	chr14:24436807-24437147	HepG2	liver:	n/a	n/a
29	JUND	chr14:24438221-24438504	HepG2	liver:	n/a	n/a
30	JUND	chr14:24437980-24439883	HepG2	liver:	n/a	chr14:24439561-24439570
31	JUND	chr14:24438536-24439548	HepG2	liver:	n/a	n/a
32	MAX	chr14:24438984-24439163	HepG2	liver:	n/a	n/a
33	MAX	chr14:24439089-24439304	K562	blood:	n/a	n/a
34	MBD4	chr14:24439015-24439395	HepG2	liver:	n/a	n/a
35	MYBL2	chr14:24438251-24440191	HepG2	liver:	n/a	n/a
36	MYBL2	chr14:24438653-24439501	HepG2	liver:	n/a	n/a
37	MYC	chr14:24439048-24439129	HUVEC	blood vessel:	n/a	n/a
38	MYC	chr14:24438688-24438838	MCF-7	breast:	n/a	chr14:24438775-24438784
39	MYC	chr14:24438934-24439425	MCF-7	breast:	n/a	n/a
40	MYC	chr14:24439017-24439038	HepG2	liver:	n/a	n/a
41	MYC	chr14:24439084-24439267	K562	blood:	n/a	n/a
42	MYC	chr14:24438677-24438679	MCF-7	breast:	n/a	n/a
43	MYC	chr14:24439039-24439250	HepG2	liver:	n/a	n/a
44	MYC	chr14:24438672-24438676	MCF-7	breast:	n/a	n/a
45	NFIC	chr14:24438759-24439193	HepG2	liver:	n/a	n/a
46	NRF1	chr14:24438807-24439216	SK-N-SH	brain:	n/a	chr14:24439078-24439092 chr14:24439078-24439089
47	PAX5	chr14:24438948-24439510	GM12878	blood:	n/a	n/a
48	POLR2A	chr14:24438807-24439099	GM12878	blood:	n/a	n/a
49	POLR2A	chr14:24438943-24439286	A549	lung:	n/a	n/a
50	POLR2A	chr14:24428410-24428599	K562	blood:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:24438909-24438959	SK-N-SH	brain:	n/a
2	chr14:24438909-24438959	BJ	skin:	n/a
3	chr14:24438909-24438959	Hepatocyte	liver:	n/a
4	chr14:24438136-24438186	BE2_C	brain:	n/a
5	chr14:24438909-24438959	PFSK-1	brain:	n/a
6	chr14:24438909-24438959	HEK293	kidney:	embryo
7	chr14:24435159-24435209	SK-N-SH	brain:	n/a
8	chr14:24438909-24438959	HRCEpiC	kidney:	n/a
9	chr14:24438909-24438959	HRE	kidney:	n/a
10	chr14:24435159-24435209	ovcar-3	ovarian:	n/a
11	chr14:24438909-24438959	GM12891	blood:	n/a
12	chr14:24438909-24438959	PrEC	prostate:	n/a
13	chr14:24438909-24438959	MCF10A-Er-Src	breast:	n/a
14	chr14:24438136-24438186	HRCEpiC	kidney:	n/a
15	chr14:24438136-24438186	HCM	heart:	n/a
16	chr14:24438909-24438959	HCT-116	colon:	n/a
17	chr14:24438909-24438959	HCPEpiC	choroid plexus:	n/a
18	chr14:24435159-24435209	HAEpiC	amniotic membrane:	n/a
19	chr14:24435159-24435209	PrEC	prostate:	n/a
20	chr14:24435159-24435209	AG04450	lung:	fetal
21	chr14:24438136-24438186	PFSK-1	brain:	n/a
22	chr14:24435159-24435209	BE2_C	brain:	n/a
23	chr14:24438136-24438186	HEEpiC	esophagus:	n/a
24	chr14:24435159-24435209	HNPCEpiC	eye:	n/a
25	chr14:24435159-24435209	GM12878	blood:	n/a
26	chr14:24438909-24438959	HMEC	breast:	n/a
27	chr14:24438136-24438186	SK-N-SH	brain:	n/a
28	chr14:24438909-24438959	SKMC	muscle:	n/a
29	chr14:24435159-24435209	IMR90	lung:	fetal
30	chr14:24438909-24438959	HUVEC	blood vessel:	n/a
31	chr14:24438909-24438959	SK-N-SH_RA	brain:	n/a
32	chr14:24435159-24435209	Caco-2	colon:	n/a
33	chr14:24438136-24438186	ProgFib	skin:	n/a
34	chr14:24435159-24435209	GM12892	blood:	n/a
35	chr14:24438909-24438959	Jurkat	blood:	n/a
36	chr14:24438136-24438186	HMEC	breast:	n/a
37	chr14:24438136-24438186	HRPEpiC	eye:	n/a
38	chr14:24438136-24438186	A549	lung:	n/a
39	chr14:24438909-24438959	Caco-2	colon:	n/a
40	chr14:24435159-24435209	HCPEpiC	choroid plexus:	n/a
41	chr14:24438909-24438959	PANC-1	pancreas:	n/a
42	chr14:24438136-24438186	PrEC	prostate:	n/a
43	chr14:24438909-24438959	MCF-7	breast:	n/a
44	chr14:24438136-24438186	AG04449	skin:	fetal
45	chr14:24435159-24435209	K562	blood:	n/a
46	chr14:24438136-24438186	HAEpiC	amniotic membrane:	n/a
47	chr14:24438909-24438959	BE2_C	brain:	n/a
48	chr14:24438136-24438186	HepG2	liver:	n/a
49	chr14:24435159-24435209	NHBE	bronchial:	n/a
50	chr14:24438136-24438186	IMR90	lung:	fetal

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr14:24421589..24424746-chr14:24425153..24428957,4	MCF-7	breast:

No data

Variant related genes	Relation type
DHRS4	TF binding region
DHRS4L2	TF binding region
DHRS4-AS1	TF binding region
DHRS4	CpG island
DHRS4L2	CpG island
DHRS4-AS1	CpG island
ENSG00000215256	chromatin interactions
ENSG00000157326	chromatin interactions

Extended variants
information (count: 503 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:503 , 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	rs554738118	chr14:24427330-24427331	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs574733312	chr14:24427338-24427339	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs540511503	chr14:24427339-24427340	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs377469993	chr14:24427342-24427343	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs73600730	chr14:24427358-24427359	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
6	rs149805904	chr14:24427377-24427378	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs367603379	chr14:24427379-24427380	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs370338389	chr14:24427417-24427418	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs375067949	chr14:24427422-24427423	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs545802043	chr14:24427439-24427440	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs562406066	chr14:24427506-24427507	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs531440918	chr14:24427519-24427520	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs372763602	chr14:24427533-24427534	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs541995143	chr14:24427547-24427548	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs549451558	chr14:24427572-24427573	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs145694444	chr14:24427573-24427574	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs527508021	chr14:24427580-24427581	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs535608697	chr14:24427581-24427582	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs552718159	chr14:24427588-24427589	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs189349458	chr14:24427621-24427622	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs180820856	chr14:24427629-24427630	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs148510671	chr14:24427630-24427631	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs186414658	chr14:24427639-24427640	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs552545155	chr14:24427710-24427711	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs73600731	chr14:24427760-24427761	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs537940428	chr14:24427762-24427763	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs554678822	chr14:24427763-24427764	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs568292859	chr14:24427765-24427766	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs35631264	chr14:24427821-24427822	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs557778210	chr14:24427827-24427828	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs35656062	chr14:24427839-24427840	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs189202356	chr14:24427845-24427846	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs375654553	chr14:24427846-24427847	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs145271891	chr14:24427860-24427861	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs147640917	chr14:24427902-24427903	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs556124092	chr14:24427912-24427913	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs142311197	chr14:24427999-24428000	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs553460896	chr14:24428036-24428037	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs541923503	chr14:24428069-24428070	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs561784820	chr14:24428084-24428085	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs527446351	chr14:24428110-24428111	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs6573483	chr14:24428141-24428142	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs151203525	chr14:24428166-24428167	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs533251784	chr14:24428167-24428168	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs549846322	chr14:24428178-24428179	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs140167952	chr14:24428191-24428192	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs531625473	chr14:24428198-24428199	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs548249276	chr14:24428209-24428210	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs367603567	chr14:24428252-24428253	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs181613242	chr14:24428270-24428271	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:62)

Disease	PMID	Source
Cancer	20164920	CNVD
Esophageal cancer	21851588	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
High-proliferative meningiomas	17937814	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	20067559	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
Breast cancer	17899364	CNVD
Colorectal cancer	16774939	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	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
Endometrioid adenocarcinoma	16974079	CNVD
Lung cancer	16773561	CNVD
Multiple myeloma	16616336	CNVD
Cancer	17440070	CNVD
Breast cancer	16272173	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Epilepsy	20736978	CNVD
Mental retardation	20736978	CNVD
severe speech impairment	20736978	CNVD
speech impairment	20736978	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Prostate cancer	18632612	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Chronic myeloid leukemia	20724749	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21804112	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	17603634	CNVD
Esophageal cancer	20955586	CNVD
Cancer	21183584	CNVD
Leukoplakia	24403051	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Breast cancer	21364760	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Glioblastoma multiforme	21390271	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:283 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:24423400-24429000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
2	chr14:24423400-24431000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr14:24423600-24430800	Weak transcription	Psoas Muscle	Psoas
4	chr14:24423600-24438800	Weak transcription	Lung	lung
5	chr14:24423600-24438800	Weak transcription	Ovary	ovary
6	chr14:24423800-24427400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
7	chr14:24423800-24427400	Weak transcription	HSMMtube	muscle
8	chr14:24423800-24429200	Weak transcription	Fetal Intestine Small	intestine
9	chr14:24423800-24430800	Weak transcription	Fetal Thymus	thymus
10	chr14:24423800-24432400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr14:24423800-24435600	Weak transcription	Primary B cells from cord blood	blood
12	chr14:24423800-24438200	Weak transcription	Primary T helper cells PMA-I stimulated	--
13	chr14:24423800-24438600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
14	chr14:24423800-24438600	Weak transcription	Primary T helper cells fromperipheralblood	blood
15	chr14:24423800-24438800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
16	chr14:24423800-24438800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
17	chr14:24423800-24438800	Weak transcription	Left Ventricle	heart
18	chr14:24423800-24438800	Weak transcription	Right Ventricle	heart
19	chr14:24423800-24438800	Weak transcription	Osteobl	bone
20	chr14:24424000-24427600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
21	chr14:24424000-24428200	Weak transcription	Brain Anterior Caudate	brain
22	chr14:24424000-24429000	Weak transcription	A549	lung
23	chr14:24424000-24435400	Weak transcription	Primary B cells from peripheral blood	blood
24	chr14:24424000-24437400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
25	chr14:24424000-24438200	Weak transcription	Primary T cells fromperipheralblood	blood
26	chr14:24424000-24438200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
27	chr14:24424000-24438800	Weak transcription	Primary hematopoietic stem cells	blood
28	chr14:24424000-24438800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
29	chr14:24424000-24438800	Weak transcription	HSMM	muscle
30	chr14:24424000-24458000	Weak transcription	Primary T cells from cord blood	blood
31	chr14:24424200-24435400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
32	chr14:24424200-24438200	Weak transcription	Rectal Smooth Muscle	rectum
33	chr14:24424200-24438800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
34	chr14:24424200-24438800	Weak transcription	NHEK	skin
35	chr14:24424400-24427400	Weak transcription	Fetal Brain Female	brain
36	chr14:24424400-24427600	Weak transcription	Skeletal Muscle Male	skeletal muscle
37	chr14:24424400-24429200	Weak transcription	Placenta	Placenta
38	chr14:24424400-24429200	Weak transcription	Sigmoid Colon	Sigmoid Colon
39	chr14:24424400-24429800	Weak transcription	Esophagus	oesophagus
40	chr14:24424400-24430000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
41	chr14:24424400-24432200	Weak transcription	Dnd41	blood
42	chr14:24424400-24436600	Weak transcription	Gastric	stomach
43	chr14:24424400-24438000	Weak transcription	Stomach Smooth Muscle	stomach
44	chr14:24424400-24438600	Weak transcription	Brain Hippocampus Middle	brain
45	chr14:24424400-24438800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
46	chr14:24424400-24438800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
47	chr14:24424400-24438800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
48	chr14:24424400-24438800	Weak transcription	Muscle Satellite Cultured Cells	--
49	chr14:24424400-24438800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
50	chr14:24424400-24438800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin

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