Variant report

Variant	rs17102923
Chromosome Location	chr14:35449839-35449840
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:14)
CpG islands
(count:0)
Chromatin interactive
region (count:7)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:14 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	GATA3	chr14:35449801-35449869	SH-SY5Y	brain:	n/a	n/a
2	MAZ	chr14:35449795-35452720	IMR90	lung:	n/a	chr14:35452357-35452366 chr14:35451986-35451994
3	MBD4	chr14:35449651-35453338	HepG2	liver:	n/a	n/a
4	MAX	chr14:35449789-35453237	HepG2	liver:	n/a	chr14:35452357-35452366 chr14:35451986-35451994
5	MYBL2	chr14:35449780-35453391	HepG2	liver:	n/a	n/a
6	MBD4	chr14:35449705-35452854	HepG2	liver:	n/a	n/a
7	TEAD4	chr14:35449669-35453202	HepG2	liver:	n/a	n/a
8	ARID3A	chr14:35449799-35452898	HepG2	liver:	n/a	chr14:35452584-35452600
9	NFIC	chr14:35449742-35452575	HepG2	liver:	n/a	n/a
10	MXI1	chr14:35449648-35453116	SK-N-SH	brain:	n/a	n/a
11	MYBL2	chr14:35449836-35453399	HepG2	liver:	n/a	n/a
12	MXI1	chr14:35449638-35453204	IMR90	lung:	n/a	n/a
13	HCFC1	chr14:35449820-35453341	Hela-S3	cervix:	n/a	n/a
14	FOXA1	chr14:35449650-35450840	HepG2	liver:	n/a	chr14:35450466-35450478

No data

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:35449513..35454029-chr14:35868261..35874094,7	MCF-7	breast:
2	chr14:35449656..35453109-chr14:35514529..35517063,4	MCF-7	breast:
3	chr14:35023701..35025768-chr14:35449276..35451419,2	K562	blood:
4	chr14:35341954..35346847-chr14:35449484..35456301,15	MCF-7	breast:
5	chr14:35341948..35345853-chr14:35449382..35453241,7	K562	blood:
6	chr14:35341867..35346512-chr14:35447191..35456965,26	MCF-7	breast:
7	chr14:35449839..35454578-chr14:35513316..35515954,7	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-BAZ1A-1	chr14:35449441-35452103	NONHSAT036355

No data

Variant related genes	Relation type
SRP54	TF binding region
ENSG00000151327	Chromatin interaction
ENSG00000100906	Chromatin interaction
ENSG00000206588	Chromatin interaction
ENSG00000198604	Chromatin interaction
ENSG00000258738	Chromatin interaction

Extended variants
information (count: 116 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:100)

rs_ID	r²[population]
rs1028449	0.82[ASN][1000 genomes]
rs11156867	0.92[ASN][1000 genomes]
rs11156868	0.92[ASN][1000 genomes]
rs11850317	0.92[ASN][1000 genomes]
rs12050171	0.83[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12050267	0.89[AMR][1000 genomes];0.93[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12050390	0.81[AFR][1000 genomes];0.81[AMR][1000 genomes];0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12050402	0.81[AFR][1000 genomes];0.81[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12050404	0.81[AFR][1000 genomes];0.81[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12050447	0.91[AFR][1000 genomes];0.85[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12161905	0.86[AFR][1000 genomes];0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12587376	0.80[ASN][1000 genomes]
rs12588755	0.93[AMR][1000 genomes];0.87[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12880809	0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12880928	0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12881698	0.87[ASN][1000 genomes]
rs12883971	0.86[AFR][1000 genomes];0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12886251	0.91[ASN][1000 genomes]
rs12887248	0.85[ASN][1000 genomes]
rs12887779	0.81[ASN][1000 genomes]
rs12888272	0.86[AFR][1000 genomes];0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12890056	0.86[AFR][1000 genomes];0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12890307	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12892056	0.91[AFR][1000 genomes];0.98[AMR][1000 genomes];0.92[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12892552	0.82[ASN][1000 genomes]
rs12893021	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12894365	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12894820	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12895051	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12895822	0.94[EUR][1000 genomes]
rs12896759	0.81[AFR][1000 genomes];0.88[ASN][1000 genomes]
rs12897044	0.89[AMR][1000 genomes];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs17102904	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs17102967	0.92[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs17102970	0.86[AFR][1000 genomes];0.92[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1967723	0.91[ASN][1000 genomes]
rs2273156	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2273158	0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2383688	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2383689	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs28373355	0.91[ASN][1000 genomes]
rs34678475	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34737707	0.85[ASN][1000 genomes]
rs34927714	0.81[EUR][1000 genomes]
rs35030792	0.83[AFR][1000 genomes];0.87[ASN][1000 genomes]
rs35090385	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs35106382	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs35337462	0.93[AMR][1000 genomes];0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs35797365	1.00[AFR][1000 genomes];0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35830406	0.92[ASN][1000 genomes]
rs35875778	0.82[EUR][1000 genomes]
rs35962127	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs36008567	0.83[AFR][1000 genomes];0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs36024417	0.85[AFR][1000 genomes];0.91[AMR][1000 genomes];0.85[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs36112862	0.84[AFR][1000 genomes];0.92[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs36159852	0.82[EUR][1000 genomes]
rs3809449	0.82[ASN][1000 genomes]
rs4573843	0.82[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4594164	0.82[ASN][1000 genomes]
rs5014384	0.82[ASN][1000 genomes]
rs56686328	0.92[AFR][1000 genomes];0.85[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs56950244	0.82[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs60693825	0.82[ASN][1000 genomes]
rs60803103	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs61125355	0.80[ASN][1000 genomes]
rs61136372	0.80[ASN][1000 genomes]
rs62625038	0.81[ASN][1000 genomes]
rs7140843	0.92[ASN][1000 genomes]
rs71409556	0.91[AMR][1000 genomes];0.84[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7141292	0.87[AFR][1000 genomes];0.82[AMR][1000 genomes];0.89[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs71421920	0.87[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs71421921	0.86[ASN][1000 genomes]
rs7143827	0.92[ASN][1000 genomes]
rs7144574	0.86[AFR][1000 genomes];0.85[AMR][1000 genomes];0.94[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7144617	0.87[ASN][1000 genomes]
rs7144646	0.90[AFR][1000 genomes];0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7145608	0.91[AFR][1000 genomes];0.85[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7149177	0.80[ASN][1000 genomes]
rs7153068	0.87[AFR][1000 genomes];0.83[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7153331	0.81[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs7153550	0.81[AFR][1000 genomes];0.87[ASN][1000 genomes]
rs7153626	0.81[ASN][1000 genomes]
rs7155696	0.87[ASN][1000 genomes]
rs74046408	0.88[AFR][1000 genomes];0.81[AMR][1000 genomes];0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs761505	0.92[ASN][1000 genomes]
rs761506	0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs8007274	0.82[ASN][1000 genomes]
rs8009093	0.82[ASN][1000 genomes]
rs8009646	0.85[AFR][1000 genomes];0.91[EUR][1000 genomes]
rs8011422	0.89[ASN][1000 genomes]
rs8013540	0.82[ASN][1000 genomes]
rs8014327	0.87[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs8014377	0.80[ASN][1000 genomes]
rs8015622	0.83[AFR][1000 genomes];0.87[ASN][1000 genomes]
rs8016566	0.84[AFR][1000 genomes];0.89[AMR][1000 genomes];0.83[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs8017191	0.88[AFR][1000 genomes];0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs8017225	0.88[AFR][1000 genomes];0.82[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs8018114	0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs8018409	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs8019179	0.99[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:16 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1052162	chr14:35245349-35451187	Weak transcription Strong transcription Flanking Active TSS Enhancers ZNF genes & repeats Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	37 gene(s)	inside rSNPs	diseases
2	nsv1053722	chr14:35257458-35465784	Enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	55 gene(s)	inside rSNPs	diseases
3	nsv1045939	chr14:35311074-35494703	Strong transcription Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	54 gene(s)	inside rSNPs	diseases
4	nsv456203	chr14:35311272-35512335	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	54 gene(s)	inside rSNPs	diseases
5	nsv564200	chr14:35311272-35512335	Weak transcription Genic enhancers Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	54 gene(s)	inside rSNPs	diseases
6	nsv901602	chr14:35367889-35571651	Weak transcription Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	52 gene(s)	inside rSNPs	diseases
7	nsv949617	chr14:35379923-35825436	Enhancers Weak transcription Strong transcription Genic enhancers Active TSS ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	73 gene(s)	inside rSNPs	diseases
8	nsv901604	chr14:35381137-35485748	Flanking Active TSS Weak transcription Active TSS Enhancers Strong transcription Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	34 gene(s)	inside rSNPs	diseases
9	nsv1043470	chr14:35398522-35754029	Active TSS Weak transcription Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	65 gene(s)	inside rSNPs	diseases
10	nsv542031	chr14:35398522-35754029	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	65 gene(s)	inside rSNPs	diseases
11	nsv1035925	chr14:35404661-35483420	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases
12	nsv901605	chr14:35409214-35512335	Enhancers Strong transcription Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	31 gene(s)	inside rSNPs	diseases
13	nsv901606	chr14:35449467-35512335	Strong transcription Weak transcription Flanking Active TSS ZNF genes & repeats Enhancers Active TSS Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	31 gene(s)	inside rSNPs	diseases
14	nsv901607	chr14:35449467-35540764	Weak transcription Strong transcription Flanking Active TSS Active TSS Genic enhancers Enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	48 gene(s)	inside rSNPs	diseases
15	nsv901608	chr14:35449467-35571651	Weak transcription ZNF genes & repeats Enhancers Strong transcription Genic enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	49 gene(s)	inside rSNPs	diseases
16	nsv901609	chr14:35449467-35587767	Weak transcription Strong transcription Flanking Active TSS Enhancers Genic enhancers ZNF genes & repeats Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	52 gene(s)	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs17102923	PPP2R3C	Cis_1M	lymphoblastoid	RTeQTL
rs17102923	PPP2R3C	cis	Whole Blood	GTEx

Chromatin state (count:110 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:35411800-35450000	Weak transcription	Brain Angular Gyrus	brain
2	chr14:35418000-35450600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr14:35420000-35450000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr14:35420000-35450000	Weak transcription	Small Intestine	intestine
5	chr14:35420400-35450200	Weak transcription	Colon Smooth Muscle	Colon
6	chr14:35421800-35450600	Weak transcription	Esophagus	oesophagus
7	chr14:35422000-35450000	Weak transcription	Brain Substantia Nigra	brain
8	chr14:35423800-35450000	Weak transcription	Colonic Mucosa	Colon
9	chr14:35425800-35450000	Weak transcription	Rectal Mucosa Donor 31	rectum
10	chr14:35425800-35450000	Weak transcription	Right Ventricle	heart
11	chr14:35425800-35450600	Weak transcription	Ovary	ovary
12	chr14:35426000-35450000	Weak transcription	Lung	lung
13	chr14:35426000-35450200	Weak transcription	Aorta	Aorta
14	chr14:35426000-35450400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
15	chr14:35426000-35450800	Weak transcription	Gastric	stomach
16	chr14:35427400-35450000	Weak transcription	Fetal Kidney	kidney
17	chr14:35427400-35450000	Weak transcription	Stomach Smooth Muscle	stomach
18	chr14:35430000-35450200	Weak transcription	Stomach Mucosa	stomach
19	chr14:35435800-35450000	Weak transcription	H1 Cell Line	embryonic stem cell
20	chr14:35436400-35450000	Weak transcription	Skeletal Muscle Female	skeletal muscle
21	chr14:35437600-35450000	Weak transcription	Fetal Muscle Trunk	muscle
22	chr14:35437800-35450000	Weak transcription	Adipose Nuclei	Adipose
23	chr14:35438000-35450000	Weak transcription	Spleen	Spleen
24	chr14:35438400-35450000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
25	chr14:35438600-35450000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
26	chr14:35438600-35450000	Weak transcription	Primary monocytes fromperipheralblood	blood
27	chr14:35438600-35450000	Weak transcription	Fetal Muscle Leg	muscle
28	chr14:35438600-35450000	Weak transcription	Fetal Stomach	stomach
29	chr14:35438600-35450000	Weak transcription	Left Ventricle	heart
30	chr14:35438600-35450000	Weak transcription	Thymus	Thymus
31	chr14:35438800-35450000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
32	chr14:35438800-35450000	Weak transcription	Primary B cells from cord blood	blood
33	chr14:35441200-35450000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
34	chr14:35441400-35450000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
35	chr14:35441400-35450000	Weak transcription	HUES6 Cell Line	embryonic stem cell
36	chr14:35441400-35450000	Weak transcription	HSMM	muscle
37	chr14:35441400-35450000	Weak transcription	HSMMtube	muscle
38	chr14:35441400-35450000	Weak transcription	Monocytes-CD14+_RO01746	blood
39	chr14:35441600-35450000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
40	chr14:35441600-35450000	Weak transcription	Primary B cells from peripheral blood	blood
41	chr14:35441600-35450000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
42	chr14:35441800-35450000	Weak transcription	NH-A	brain
43	chr14:35445400-35450000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
44	chr14:35445400-35450000	Weak transcription	Pancreas	Pancrea
45	chr14:35446600-35450000	Weak transcription	Fetal Thymus	thymus
46	chr14:35447400-35450000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
47	chr14:35447400-35450000	Weak transcription	Fetal Intestine Small	intestine
48	chr14:35449000-35450000	Enhancers	Primary T helper cells fromperipheralblood	blood
49	chr14:35449200-35450000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
50	chr14:35449200-35450000	Enhancers	Primary T helper cells PMA-I stimulated	--

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