Variant report

Variant	rs2952819
Chromosome Location	chr4:151932855-151932856
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr4:151931291..151933341-chr4:151934624..151937795,5	K562	blood:
2	chr4:151931707..151933572-chr4:152019446..152021222,2	MCF-7	breast:
3	chr4:151932388..151938493-chr4:152018908..152023577,12	K562	blood:
4	chr4:151932388..151938967-chr4:152018772..152026013,16	K562	blood:

Variant related genes	Relation type
ENSG00000201264	Chromatin interaction
ENSG00000208797	Chromatin interaction
ENSG00000198589	Chromatin interaction
ENSG00000145425	Chromatin interaction

Extended variants
information (count: 100 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:68)

rs_ID	r²[population]
rs10034173	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10222881	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1148631	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1148633	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1148634	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1148636	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1148641	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1148644	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1148646	0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1148650	0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1148651	0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1148655	0.80[EUR][1000 genomes]
rs11734095	0.91[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1201197	0.91[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1201199	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1201200	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1201208	0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1201209	0.81[AFR][1000 genomes];0.88[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1201210	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1201216	0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1212119	0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12501829	0.86[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1273329	0.86[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1273331	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1273332	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1298678	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1583188	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1583189	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1615230	0.86[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs17027155	0.84[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs17027197	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17027226	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1782360	0.80[EUR][1000 genomes]
rs1782365	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1975112	0.86[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2154349	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2912477	0.84[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2915451	0.84[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs294532	0.80[EUR][1000 genomes]
rs294533	0.80[EUR][1000 genomes]
rs2952814	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2952817	0.82[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2952818	0.86[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3990470	0.98[ASN][1000 genomes]
rs4524364	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4696648	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs57003564	0.84[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs57029739	0.84[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62344602	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62344619	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62344622	0.84[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62344623	0.84[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62344624	0.97[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6535756	0.81[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6535757	0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6535760	0.91[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6812083	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6833956	0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6839352	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7436602	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7657953	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7677374	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7678748	0.88[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7683377	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7684325	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7693282	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs891689	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9999064	0.92[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:32 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1024820	chr4:151364078-151943561	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
2	nsv1034948	chr4:151590115-152202687	Weak transcription Strong transcription Enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
3	nsv537302	chr4:151590115-152202687	ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS Enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
4	nsv530159	chr4:151624865-152203910	Weak transcription Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
5	nsv1018404	chr4:151664438-152067409	Weak transcription Flanking Active TSS Strong transcription Enhancers Active TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
6	nsv1017850	chr4:151664438-152071876	Active TSS Weak transcription Strong transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
7	esv2763837	chr4:151664438-152071888	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
8	nsv870257	chr4:151665349-152072867	Strong transcription Weak transcription Active TSS Genic enhancers Flanking Active TSS Enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
9	nsv1015387	chr4:151673751-152071876	Weak transcription Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
10	nsv526976	chr4:151675819-152055073	Weak transcription Flanking Active TSS Enhancers Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
11	nsv1025077	chr4:151682266-152035733	Strong transcription Enhancers Flanking Active TSS Genic enhancers Active TSS Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	31 gene(s)	inside rSNPs	diseases
12	nsv537303	chr4:151682266-152035733	Strong transcription Weak transcription Genic enhancers Enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	31 gene(s)	inside rSNPs	diseases
13	nsv949066	chr4:151693149-152069566	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Bivalent/Poised TSS ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
14	nsv949002	chr4:151693149-152095109	Strong transcription Weak transcription Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
15	nsv948719	chr4:151693149-152161625	Weak transcription Bivalent/Poised TSS Strong transcription Genic enhancers Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
16	nsv1031720	chr4:151708502-152071876	Strong transcription Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
17	nsv880262	chr4:151712054-152519899	Enhancers Weak transcription Strong transcription Bivalent Enhancer Active TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	53 gene(s)	inside rSNPs	diseases
18	nsv1031516	chr4:151718614-152065644	Weak transcription Enhancers Strong transcription Active TSS ZNF genes & repeats Flanking Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
19	nsv537304	chr4:151718614-152065644	Flanking Active TSS Weak transcription Strong transcription Enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
20	nsv1022884	chr4:151718814-152065505	Strong transcription Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
21	nsv537305	chr4:151718814-152065505	Enhancers Weak transcription Transcr. at gene 5' and 3' Strong transcription Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
22	nsv880576	chr4:151751369-151936149	Weak transcription Strong transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	12 gene(s)	inside rSNPs	diseases
23	nsv595689	chr4:151788955-152015704	Enhancers Active TSS Strong transcription Weak transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
24	nsv595690	chr4:151788955-152109552	Enhancers Strong transcription Weak transcription Flanking Active TSS Bivalent Enhancer Genic enhancers Active TSS 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 miRNA target site	35 gene(s)	inside rSNPs	diseases
25	nsv881254	chr4:151829824-151936149	Bivalent/Poised TSS Flanking Active TSS Weak transcription Strong transcription Active TSS Enhancers ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	12 gene(s)	inside rSNPs	diseases
26	nsv880429	chr4:151844476-151936149	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	12 gene(s)	inside rSNPs	diseases
27	nsv1026416	chr4:151847403-152105879	Transcr. at gene 5' and 3' Enhancers Strong transcription Flanking Active TSS Weak transcription Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
28	nsv461678	chr4:151865522-151980636	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Strong transcription 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	23 gene(s)	inside rSNPs	diseases
29	nsv595692	chr4:151865522-151980636	Flanking Active TSS Strong transcription Enhancers Weak transcription Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
30	nsv595699	chr4:151880765-151968295	Enhancers Active TSS Flanking Active TSS Strong transcription Weak transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
31	nsv869553	chr4:151892289-152003402	Enhancers Strong transcription Active TSS Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
32	nsv1018797	chr4:151913585-152073419	Flanking Active TSS Active TSS Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers Strong transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:85 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:151888800-151933400	Weak transcription	Fetal Lung	lung
2	chr4:151894000-151933200	Weak transcription	Rectal Mucosa Donor 29	rectum
3	chr4:151904200-151935600	Weak transcription	Aorta	Aorta
4	chr4:151916400-151933000	Weak transcription	Primary T cells from cord blood	blood
5	chr4:151917200-151933200	Weak transcription	HepG2	liver
6	chr4:151920000-151935400	Weak transcription	Fetal Muscle Trunk	muscle
7	chr4:151920400-151933000	Weak transcription	Primary hematopoietic stem cells	blood
8	chr4:151920800-151933600	Weak transcription	Monocytes-CD14+_RO01746	blood
9	chr4:151920800-151934000	Weak transcription	Primary monocytes fromperipheralblood	blood
10	chr4:151920800-151934000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
11	chr4:151921200-151933000	Weak transcription	Primary B cells from cord blood	blood
12	chr4:151921400-151934200	Weak transcription	Rectal Smooth Muscle	rectum
13	chr4:151921600-151933000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
14	chr4:151921600-151934000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
15	chr4:151921800-151934000	Weak transcription	Cortex derived primary cultured neurospheres	brain
16	chr4:151921800-151934400	Weak transcription	Colonic Mucosa	Colon
17	chr4:151922000-151934000	Weak transcription	Fetal Muscle Leg	muscle
18	chr4:151922200-151933200	Weak transcription	Thymus	Thymus
19	chr4:151922200-151934000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
20	chr4:151922400-151933600	Weak transcription	HUES48 Cell Line	embryonic stem cell
21	chr4:151922600-151933000	Strong transcription	Fetal Intestine Small	intestine
22	chr4:151922600-151935600	Weak transcription	Lung	lung
23	chr4:151922800-151933000	Weak transcription	Sigmoid Colon	Sigmoid Colon
24	chr4:151922800-151934000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
25	chr4:151922800-151935400	Weak transcription	Placenta	Placenta
26	chr4:151922800-151935600	Weak transcription	Esophagus	oesophagus
27	chr4:151923000-151934000	Weak transcription	H9 Cell Line	embryonic stem cell
28	chr4:151923000-151934000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
29	chr4:151923000-151935200	Weak transcription	Ovary	ovary
30	chr4:151923000-151935400	Weak transcription	Pancreas	Pancrea
31	chr4:151923000-151935600	Weak transcription	Gastric	stomach
32	chr4:151923200-151933000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
33	chr4:151923200-151933200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
34	chr4:151923200-151933200	Weak transcription	Primary B cells from peripheral blood	blood
35	chr4:151923200-151933600	Weak transcription	H1 Cell Line	embryonic stem cell
36	chr4:151923200-151934600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
37	chr4:151923200-151935600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
38	chr4:151923600-151933800	Weak transcription	A549	lung
39	chr4:151924000-151934800	Weak transcription	Stomach Smooth Muscle	stomach
40	chr4:151925000-151934200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
41	chr4:151925400-151933800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
42	chr4:151925600-151934400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
43	chr4:151925800-151933600	Weak transcription	Fetal Intestine Large	intestine
44	chr4:151925800-151934000	Weak transcription	Muscle Satellite Cultured Cells	--
45	chr4:151925800-151934200	Weak transcription	NH-A	brain
46	chr4:151926200-151933200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
47	chr4:151926200-151933200	Weak transcription	HMEC	breast
48	chr4:151926200-151933600	Weak transcription	NHEK	skin
49	chr4:151926200-151934200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
50	chr4:151926400-151933200	Weak transcription	Hela-S3	cervix

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