Variant report

Variant	nsv901610
Chromosome Location	chr14:35470049-35509571
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:121)
CpG islands
(count:122)
Chromatin interactive
region (count:21)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:121 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:35509539-35510010	HepG2	liver:	n/a	chr14:35509792-35509808
2	ATF2	chr14:35504149-35504484	GM12878	blood:	n/a	n/a
3	BATF	chr14:35502850-35503057	GM12878	blood:	n/a	chr14:35502942-35502953
4	BATF	chr14:35504265-35504563	GM12878	blood:	n/a	chr14:35504383-35504394
5	BATF	chr14:35504189-35504612	GM12878	blood:	n/a	chr14:35504383-35504394
6	BATF	chr14:35502715-35503130	GM12878	blood:	n/a	chr14:35502942-35502953
7	BCL11A	chr14:35504236-35504481	GM12878	blood:	n/a	n/a
8	CBX3	chr14:35503606-35504100	K562	blood:	n/a	n/a
9	CBX3	chr14:35503722-35504021	K562	blood:	n/a	n/a
10	CEBPB	chr14:35502339-35502472	HepG2	liver:	n/a	n/a
11	CEBPB	chr14:35471969-35472090	IMR90	lung:	n/a	n/a
12	CEBPB	chr14:35506053-35506254	HepG2	liver:	n/a	n/a
13	CTCF	chr14:35497448-35497638	GM12878	blood:	n/a	n/a
14	CTCF	chr14:35500542-35500599	Fibrobl	skin:	n/a	n/a
15	CTCF	chr14:35476333-35476336	Kidney_OC	kidney:	n/a	n/a
16	CTCF	chr14:35477260-35477410	MCF-7	breast:	n/a	n/a
17	CTCF	chr14:35503977-35504048	GM10248	blood:	n/a	n/a
18	CTCF	chr14:35498177-35498262	Lung_OC	lung:	n/a	n/a
19	CTCF	chr14:35474821-35474902	GM20000	blood:	n/a	n/a
20	CTCF	chr14:35509513-35510126	A549	lung:	n/a	chr14:35509912-35509933 chr14:35509910-35509928 chr14:35509913-35509922
21	CTCF	chr14:35476343-35476350	Kidney_OC	kidney:	n/a	n/a
22	CTCF	chr14:35503340-35503490	HepG2	liver:	n/a	n/a
23	EBF1	chr14:35505498-35505780	GM12878	blood:	n/a	n/a
24	EBF1	chr14:35504201-35504475	GM12878	blood:	n/a	chr14:35504330-35504341
25	EBF1	chr14:35504214-35504458	GM12878	blood:	n/a	chr14:35504330-35504341
26	FAM48A	chr14:35470090-35470278	GM12878	blood:	n/a	n/a
27	FOS	chr14:35471899-35471944	MCF10A-Er-Src	breast:	n/a	n/a
28	FOS	chr14:35494566-35494592	MCF10A-Er-Src	breast:	n/a	n/a
29	FOS	chr14:35471862-35472051	MCF10A-Er-Src	breast:	n/a	n/a
30	FOSL2	chr14:35502850-35504038	HepG2	liver:	n/a	n/a
31	FOSL2	chr14:35504224-35504657	HepG2	liver:	n/a	n/a
32	FOXA1	chr14:35502937-35503467	HepG2	liver:	n/a	n/a
33	FOXA2	chr14:35472607-35472995	A549	lung:	n/a	n/a
34	GABPA	chr14:35476254-35476364	GM12878	blood:	n/a	n/a
35	GATA3	chr14:35494451-35494906	SH-SY5Y	brain:	n/a	chr14:35494738-35494759 chr14:35494745-35494752 chr14:35494745-35494752 chr14:35494745-35494752 chr14:35494741-35494757
36	GATA3	chr14:35497613-35497842	SH-SY5Y	brain:	n/a	n/a
37	HNF4A	chr14:35504446-35504633	HepG2	liver:	n/a	chr14:35504530-35504545
38	HNF4G	chr14:35504401-35504651	HepG2	liver:	n/a	chr14:35504529-35504544
39	IRF3	chr14:35490039-35490071	GM12878	blood:	n/a	n/a
40	IRF4	chr14:35504159-35504573	GM12878	blood:	n/a	n/a
41	IRF4	chr14:35504277-35504651	GM12878	blood:	n/a	n/a
42	JUND	chr14:35474062-35474174	HepG2	liver:	n/a	n/a
43	JUND	chr14:35503129-35503624	HepG2	liver:	n/a	n/a
44	JUND	chr14:35494611-35494811	HepG2	liver:	n/a	chr14:35494659-35494670
45	JUND	chr14:35509529-35509826	HepG2	liver:	n/a	chr14:35509649-35509660 chr14:35509555-35509564
46	KAP1	chr14:35503554-35504027	HEK293	kidney:	n/a	n/a
47	KAP1	chr14:35503614-35504021	K562	blood:	n/a	n/a
48	KAP1	chr14:35503677-35503950	U2OS	brain:	n/a	n/a
49	MAFF	chr14:35470841-35471187	K562	blood:	n/a	chr14:35471016-35471034
50	MAFF	chr14:35470810-35471209	HepG2	liver:	n/a	chr14:35471016-35471034

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:35498490-35498540	RPTEC	kidney:	n/a
2	chr14:35498490-35498540	NHBE	bronchial:	n/a
3	chr14:35495536-35495586	GM19239	blood:	n/a
4	chr14:35495536-35495586	NH-A	brain:	n/a
5	chr14:35495536-35495586	SAEC	small airway:	n/a
6	chr14:35495536-35495586	HIPEpiC	eye:	n/a
7	chr14:35495536-35495586	LNCaP	prostate:	n/a
8	chr14:35495536-35495586	ProgFib	skin:	n/a
9	chr14:35498490-35498540	A549	lung:	n/a
10	chr14:35495536-35495586	HUVEC	blood vessel:	n/a
11	chr14:35495536-35495586	A549	lung:	n/a
12	chr14:35495536-35495586	MCF-7	breast:	n/a
13	chr14:35498490-35498540	ovcar-3	ovarian:	n/a
14	chr14:35495536-35495586	K562	blood:	n/a
15	chr14:35498490-35498540	PANC-1	pancreas:	n/a
16	chr14:35495536-35495586	AG04450	lung:	fetal
17	chr14:35495536-35495586	GM12892	blood:	n/a
18	chr14:35498490-35498540	HCPEpiC	choroid plexus:	n/a
19	chr14:35495536-35495586	Jurkat	blood:	n/a
20	chr14:35498490-35498540	HRE	kidney:	n/a
21	chr14:35498490-35498540	T-47D	breast:	n/a
22	chr14:35498490-35498540	NHDF-neo	bronchial:	n/a
23	chr14:35498490-35498540	AG09309	skin:	n/a
24	chr14:35495536-35495586	IMR90	lung:	fetal
25	chr14:35498490-35498540	HNPCEpiC	eye:	n/a
26	chr14:35498490-35498540	NT2-D1	testis:	n/a
27	chr14:35495536-35495586	HepG2	liver:	n/a
28	chr14:35495536-35495586	Caco-2	colon:	n/a
29	chr14:35498490-35498540	HCF	heart:	n/a
30	chr14:35495536-35495586	HRPEpiC	eye:	n/a
31	chr14:35498490-35498540	HRCEpiC	kidney:	n/a
32	chr14:35495536-35495586	AG10803	skin:	n/a
33	chr14:35498490-35498540	PrEC	prostate:	n/a
34	chr14:35498490-35498540	GM12891	blood:	n/a
35	chr14:35498490-35498540	ProgFib	skin:	n/a
36	chr14:35498490-35498540	HRPEpiC	eye:	n/a
37	chr14:35495536-35495586	RPTEC	kidney:	n/a
38	chr14:35498490-35498540	AG04450	lung:	fetal
39	chr14:35495536-35495586	GM12878	blood:	n/a
40	chr14:35495536-35495586	SKMC	muscle:	n/a
41	chr14:35498490-35498540	HL-60	blood:	n/a
42	chr14:35495536-35495586	SK-N-SH	brain:	n/a
43	chr14:35495536-35495586	GM06990	blood:	n/a
44	chr14:35495536-35495586	HCF	heart:	n/a
45	chr14:35495536-35495586	AG09319	gingival:	n/a
46	chr14:35495536-35495586	SK-N-SH_RA	brain:	n/a
47	chr14:35498490-35498540	GM06990	blood:	n/a
48	chr14:35498490-35498540	MCF10A-Er-Src	breast:	n/a
49	chr14:35498490-35498540	HAEpiC	amniotic membrane:	n/a
50	chr14:35498490-35498540	NH-A	brain:	n/a

(count:21 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:35499235..35502810-chr14:35514800..35516736,3	MCF-7	breast:
2	chr14:35479120..35481576-chr14:35483868..35486347,2	MCF-7	breast:
3	chr14:35500095..35502926-chr14:35557815..35560264,2	MCF-7	breast:
4	chr14:35507467..35509940-chr14:35513836..35516152,2	MCF-7	breast:
5	chr14:35500902..35503626-chr14:35810015..35811675,2	MCF-7	breast:
6	chr14:35473349..35476278-chr14:35514310..35517232,2	MCF-7	breast:
7	chr14:35466324..35467917-chr14:35470934..35473111,2	K562	blood:
8	chr14:35489417..35492128-chr14:35497418..35499039,2	K562	blood:
9	chr14:35492619..35494488-chr14:35513893..35516711,2	MCF-7	breast:
10	chr14:35462942..35465025-chr14:35469219..35471008,2	MCF-7	breast:
11	chr14:35508976..35512360-chr14:35513729..35517203,6	K562	blood:
12	chr14:35484859..35486804-chr14:35511078..35512949,2	K562	blood:
13	chr14:35465599..35469103-chr14:35471087..35474391,3	MCF-7	breast:
14	chr14:35506932..35507762-chr3:185524185..185525086,2	MCF-7	breast:
15	chr14:35505958..35507461-chr14:35513757..35515783,2	K562	blood:
16	chr14:35489417..35492128-chr14:35497418..35499039,2	K562	blood:
17	chr14:35343382..35345457-chr14:35494554..35496991,2	MCF-7	breast:
18	chr14:35481674..35484183-chr14:35515641..35517435,2	MCF-7	breast:
19	chr14:35339842..35342583-chr14:35472313..35474482,2	K562	blood:
20	chr14:35343911..35346253-chr14:35481173..35482947,2	MCF-7	breast:
21	chr14:35509386..35510378-chr14:35891186..35892042,3	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAM177A1-2	chr14:35487835-35487971	NONHSAT036358
2	lnc-FAM177A1-2	chr14:35488172-35488564	NONHSAT036358

No data

Variant related genes	Relation type
SRP54	TF binding region
FAM177A1	TF binding region
SRP54	CpG island
FAM177A1	CpG island
ENSG00000151327	chromatin interactions
ENSG00000198604	chromatin interactions
ENSG00000258738	chromatin interactions
ENSG00000100883	chromatin interactions

Extended variants
information (count: 1494 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:1494 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs8017225	chr14:35470049-35470050	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs574980040	chr14:35470052-35470053	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs542684804	chr14:35470085-35470086	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs376162642	chr14:35470095-35470096	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs562606208	chr14:35470103-35470104	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs531449635	chr14:35470115-35470116	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs371624971	chr14:35470235-35470236	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs184175213	chr14:35470239-35470240	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs369210450	chr14:35470311-35470312	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs144379252	chr14:35470347-35470348	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs372655232	chr14:35470372-35470373	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs564874982	chr14:35470375-35470376	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs10637082	chr14:35470381-35470382	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs397952730	chr14:35470398-35470399	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs200370367	chr14:35470399-35470400	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs8017611	chr14:35470415-35470416	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
17	rs149344644	chr14:35470502-35470503	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs567454510	chr14:35470503-35470504	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs536087850	chr14:35470572-35470573	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs549849886	chr14:35470577-35470578	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs189876602	chr14:35470595-35470596	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs538770567	chr14:35470599-35470600	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs199624631	chr14:35470603-35470604	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs200588013	chr14:35470606-35470607	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs572118243	chr14:35470609-35470610	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs546029657	chr14:35470672-35470673	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs79905967	chr14:35470754-35470755	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs12893346	chr14:35470757-35470758	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs12893022	chr14:35470765-35470766	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs554990103	chr14:35470783-35470784	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs12893180	chr14:35470797-35470798	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs181152092	chr14:35470841-35470842	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs543618254	chr14:35470850-35470851	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs563892776	chr14:35470855-35470856	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs576156681	chr14:35471001-35471002	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs545130919	chr14:35471018-35471019	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs552143681	chr14:35471030-35471031	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs111688305	chr14:35471088-35471089	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs538506498	chr14:35471147-35471148	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs375251520	chr14:35471185-35471186	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs554260529	chr14:35471225-35471226	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs527341615	chr14:35471260-35471261	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs547650024	chr14:35471276-35471277	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs540103266	chr14:35471282-35471283	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs561064601	chr14:35471283-35471284	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs12878970	chr14:35471286-35471287	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
47	rs549536743	chr14:35471315-35471316	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs569518565	chr14:35471338-35471339	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs186170176	chr14:35471344-35471345	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs61989479	chr14:35471354-35471355	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance

Variant related diseases (count:57)

Disease	PMID	Source
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
Colorectal cancer	16774939	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
Endometrioid adenocarcinoma	16974079	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Chronic myeloid leukemia	20724749	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Wilms tumour	21544195	CNVD
Esophageal cancer	20955586	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Burkitt''s lymphoma	19759907	CNVD
Lung cancer	18438408	CNVD
Urothelial carcinoma	21177765	CNVD
Multiple myeloma	17550852	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21045282	CNVD
Cancer	21129771	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Lung cancer	17925434	CNVD
Colorectal cancer	16272173	CNVD
Glioma	24330732	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21858162	CNVD
Lung cancer	21569311	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1035 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:35452800-35478200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr14:35453200-35474200	Weak transcription	Aorta	Aorta
3	chr14:35453600-35470600	Weak transcription	Fetal Stomach	stomach
4	chr14:35453600-35474200	Weak transcription	Right Ventricle	heart
5	chr14:35453600-35485600	Weak transcription	HSMMtube	muscle
6	chr14:35453800-35472000	Weak transcription	Skeletal Muscle Female	skeletal muscle
7	chr14:35453800-35473600	Weak transcription	Fetal Lung	lung
8	chr14:35453800-35474000	Weak transcription	NHEK	skin
9	chr14:35453800-35476000	Weak transcription	Rectal Smooth Muscle	rectum
10	chr14:35453800-35499200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
11	chr14:35454000-35479200	Weak transcription	Gastric	stomach
12	chr14:35454400-35471200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
13	chr14:35454400-35481600	Weak transcription	HMEC	breast
14	chr14:35454400-35485200	Weak transcription	Esophagus	oesophagus
15	chr14:35454400-35509800	Weak transcription	Psoas Muscle	Psoas
16	chr14:35454600-35474000	Weak transcription	Brain Angular Gyrus	brain
17	chr14:35454800-35471600	Weak transcription	Ovary	ovary
18	chr14:35454800-35471800	Weak transcription	Sigmoid Colon	Sigmoid Colon
19	chr14:35454800-35472000	Weak transcription	Muscle Satellite Cultured Cells	--
20	chr14:35454800-35474000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
21	chr14:35454800-35481600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
22	chr14:35454800-35483600	Weak transcription	Small Intestine	intestine
23	chr14:35454800-35484800	Weak transcription	Fetal Brain Male	brain
24	chr14:35455000-35470600	Weak transcription	Brain Inferior Temporal Lobe	brain
25	chr14:35455200-35470600	Weak transcription	NH-A	brain
26	chr14:35455200-35477200	Weak transcription	Colon Smooth Muscle	Colon
27	chr14:35455200-35482800	Weak transcription	A549	lung
28	chr14:35455200-35487200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
29	chr14:35455400-35473400	Weak transcription	Fetal Brain Female	brain
30	chr14:35455600-35481600	Weak transcription	NHLF	lung
31	chr14:35455800-35473600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
32	chr14:35456400-35472000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
33	chr14:35456400-35483400	Weak transcription	Pancreas	Pancrea
34	chr14:35457000-35477200	Weak transcription	Hela-S3	cervix
35	chr14:35459400-35470600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
36	chr14:35459400-35480200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
37	chr14:35462800-35476000	Weak transcription	HUVEC	blood vessel
38	chr14:35464000-35477200	Weak transcription	Brain Anterior Caudate	brain
39	chr14:35464000-35478000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
40	chr14:35464000-35480200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
41	chr14:35464200-35470600	Weak transcription	Placenta Amnion	Placenta Amnion
42	chr14:35464200-35474200	Weak transcription	Thymus	Thymus
43	chr14:35465200-35472200	Weak transcription	GM12878-XiMat	blood
44	chr14:35465200-35500600	Strong transcription	HepG2	liver
45	chr14:35465600-35471000	Strong transcription	Primary B cells from cord blood	blood
46	chr14:35465600-35474200	Weak transcription	Fetal Kidney	kidney
47	chr14:35465600-35475000	Strong transcription	Primary monocytes fromperipheralblood	blood
48	chr14:35465600-35482400	Weak transcription	Brain Hippocampus Middle	brain
49	chr14:35465600-35500200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr14:35465800-35474400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived

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