Variant report

Variant	rs9379821
Chromosome Location	chr6:26054268-26054269
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:24)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:24 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:65269359..65272329-chr6:26053784..26056482,2	K562	blood:
2	chr6:26053301..26055998-chr6:43904992..43907240,2	K562	blood:
3	chr6:26052367..26055979-chr6:26593142..26597982,4	K562	blood:
4	chr10:103990488..103991234-chr6:26054184..26054932,2	Hela-S3	cervix:
5	chr6:26052762..26068184-chr6:26093226..26113078,68	MCF-7	breast:
6	chr6:26053749..26055733-chr6:27045370..27048111,2	K562	blood:
7	chr17:59674398..59676539-chr6:26054195..26055908,2	MCF-7	breast:
8	chr6:26053512..26063692-chr6:26116837..26127451,29	MCF-7	breast:
9	chr5:137802996..137805932-chr6:26052839..26055494,2	K562	blood:
10	chr6:26054191..26059059-chr6:27859322..27865313,6	K562	blood:
11	chr6:26053433..26055851-chr7:100290372..100293044,2	MCF-7	breast:
12	chr17:45751302..45753563-chr6:26054221..26056562,2	MCF-7	breast:
13	chr12:6980147..6981944-chr6:26052824..26055777,2	K562	blood:
14	chr6:26053058..26056960-chr6:27797302..27800295,3	MCF-7	breast:
15	chr6:26053203..26055330-chr6:26233618..26235663,2	MCF-7	breast:
16	chr22:23522566..23524379-chr6:26053067..26054822,2	K562	blood:
17	chr17:59503555..59506189-chr6:26053990..26056536,2	MCF-7	breast:
18	chr6:26051079..26061905-chr6:26152751..26161537,32	MCF-7	breast:
19	chr6:26053810..26056149-chr6:26091394..26093038,2	MCF-7	breast:
20	chr6:26052973..26057907-chr6:27859322..27863269,5	K562	blood:
21	chr6:26053886..26056754-chr6:27838528..27841562,3	MCF-7	breast:
22	chr6:26052592..26054578-chr6:27776526..27779237,2	K562	blood:
23	chr10:97889116..97891227-chr6:26053790..26056184,2	K562	blood:
24	chr21:44845672..44847781-chr6:26053868..26056749,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000180573	Chromatin interaction
ENSG00000197153	Chromatin interaction
ENSG00000196331	Chromatin interaction
ENSG00000203813	Chromatin interaction
ENSG00000177853	Chromatin interaction
ENSG00000233224	Chromatin interaction
ENSG00000180596	Chromatin interaction
ENSG00000168298	Chromatin interaction
ENSG00000197914	Chromatin interaction
ENSG00000158373	Chromatin interaction
ENSG00000142178	Chromatin interaction
ENSG00000187475	Chromatin interaction
ENSG00000198558	Chromatin interaction
ENSG00000251562	Chromatin interaction
ENSG00000146109	Chromatin interaction
ENSG00000182572	Chromatin interaction
ENSG00000124575	Chromatin interaction
ENSG00000197061	Chromatin interaction

Extended variants
information (count: 85 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:64)

rs_ID	r²[population]
rs1061482	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10807006	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10807007	0.94[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs1130000	0.95[JPT][hapmap];0.83[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs12195653	0.85[JPT][hapmap]
rs1539183	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1800702	0.89[CHB][hapmap];1.00[JPT][hapmap];0.86[AMR][1000 genomes];0.91[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1971509	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2006736	0.89[CHB][hapmap];1.00[JPT][hapmap];0.86[AMR][1000 genomes];0.91[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2013063	1.00[JPT][hapmap];0.83[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs2032443	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2032445	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2032449	0.89[CHB][hapmap];1.00[JPT][hapmap];0.83[YRI][hapmap];0.97[AFR][1000 genomes];0.97[AMR][1000 genomes];0.90[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2032450	1.00[JPT][hapmap];0.83[AMR][1000 genomes]
rs2051544	0.88[CHB][hapmap];1.00[JPT][hapmap];0.82[YRI][hapmap];0.94[AFR][1000 genomes];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2157050	0.82[CHB][hapmap];1.00[JPT][hapmap];0.89[AMR][1000 genomes];0.87[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2328903	0.84[JPT][hapmap]
rs2328905	0.84[AMR][1000 genomes];0.90[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2794719	0.88[CHB][hapmap];1.00[JPT][hapmap];0.86[AMR][1000 genomes];0.91[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2794720	0.89[CHB][hapmap];1.00[JPT][hapmap];0.86[AMR][1000 genomes];0.91[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2858993	0.89[AFR][1000 genomes];0.89[AMR][1000 genomes];0.91[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2876693	0.84[JPT][hapmap]
rs2876694	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs3752419	0.88[CHB][hapmap];0.95[JPT][hapmap];0.82[YRI][hapmap];0.97[AFR][1000 genomes];0.94[AMR][1000 genomes];0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs3752420	0.94[CHB][hapmap];0.95[JPT][hapmap];0.82[YRI][hapmap];0.94[AFR][1000 genomes];0.97[AMR][1000 genomes];0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4529296	0.89[CHB][hapmap];1.00[JPT][hapmap];0.86[AMR][1000 genomes];0.91[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6928717	0.97[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs6928951	0.83[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs6938083	0.92[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs6942196	0.88[CHB][hapmap];1.00[JPT][hapmap];0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7738854	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7753253	0.93[CHB][hapmap];0.95[JPT][hapmap];0.91[AMR][1000 genomes];0.91[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7753826	0.83[YRI][hapmap];0.85[AFR][1000 genomes]
rs7766342	0.87[ASN][1000 genomes]
rs7772312	0.89[CHB][hapmap];1.00[JPT][hapmap];0.83[YRI][hapmap];1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9295684	0.90[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs9295685	0.89[CHB][hapmap];0.90[JPT][hapmap];0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs9295686	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9295687	0.88[CHB][hapmap];1.00[JPT][hapmap];0.86[AMR][1000 genomes];0.91[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs9295688	0.89[CHB][hapmap];1.00[JPT][hapmap];0.83[YRI][hapmap];0.87[AFR][1000 genomes];0.88[AMR][1000 genomes];0.91[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs9348706	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9356998	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9358896	0.84[JPT][hapmap]
rs9358902	0.91[AFR][1000 genomes];0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9358903	0.92[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs9358904	0.94[AFR][1000 genomes];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9358905	0.86[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs9366634	0.88[CHB][hapmap];1.00[JPT][hapmap];0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9366636	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9379818	0.88[AMR][1000 genomes]
rs9379819	0.94[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs9379820	0.83[CHB][hapmap];1.00[JPT][hapmap];0.83[YRI][hapmap];1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs9379823	0.91[AFR][1000 genomes];0.89[AMR][1000 genomes];0.92[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9379825	0.89[CHB][hapmap];1.00[JPT][hapmap];0.83[YRI][hapmap];0.91[AFR][1000 genomes];0.89[AMR][1000 genomes];0.91[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs9393681	0.84[AMR][1000 genomes]
rs9393683	0.92[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs9393684	0.88[AFR][1000 genomes];0.90[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs9461229	0.83[ASN][1000 genomes]
rs9461230	0.88[AMR][1000 genomes]
rs9467646	0.84[JPT][hapmap]
rs9467658	0.85[AMR][1000 genomes]
rs9467662	0.89[AMR][1000 genomes];0.87[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs9467663	0.84[AFR][1000 genomes];0.93[AMR][1000 genomes];0.87[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs9467672	0.89[CHB][hapmap];1.00[JPT][hapmap];0.83[YRI][hapmap];0.91[AFR][1000 genomes];0.89[AMR][1000 genomes];0.91[EUR][1000 genomes];0.87[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:21 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1029920	chr6:25638507-26585842	Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Enhancers Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Active TSS Genic enhancers Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	1215 gene(s)	inside rSNPs	diseases
2	nsv538162	chr6:25638507-26585842	Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Weak transcription Strong transcription Enhancers 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	1215 gene(s)	inside rSNPs	diseases
3	nsv1030351	chr6:25813178-26352046	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1189 gene(s)	inside rSNPs	diseases
4	nsv1023453	chr6:25853830-26528250	Weak transcription Flanking Active TSS Enhancers Active TSS Bivalent/Poised TSS Strong transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	1201 gene(s)	inside rSNPs	diseases
5	nsv1025237	chr6:25874326-26280867	Flanking Active TSS Active TSS Enhancers Weak transcription Bivalent/Poised TSS Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1166 gene(s)	inside rSNPs	diseases
6	nsv538163	chr6:25874326-26280867	Enhancers Flanking Active TSS Strong transcription Active TSS Weak transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1166 gene(s)	inside rSNPs	diseases
7	nsv432857	chr6:25957109-26072445	Flanking Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Active TSS Strong transcription Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	451 gene(s)	inside rSNPs	diseases
8	nsv1015627	chr6:25973495-26100483	Weak transcription Flanking Active TSS Active TSS Enhancers Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	447 gene(s)	inside rSNPs	diseases
9	nsv538164	chr6:25973495-26100483	Active TSS Enhancers Weak transcription Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	447 gene(s)	inside rSNPs	diseases
10	nsv1028456	chr6:25984457-26174993	Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	873 gene(s)	inside rSNPs	diseases
11	nsv538165	chr6:25984457-26174993	Active TSS Weak transcription Bivalent Enhancer Flanking Active TSS Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	873 gene(s)	inside rSNPs	diseases
12	nsv428137	chr6:25987413-26351920	Enhancers Flanking Active TSS Active TSS Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1181 gene(s)	inside rSNPs	diseases
13	nsv916992	chr6:25991630-26280921	Active TSS Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1159 gene(s)	inside rSNPs	diseases
14	nsv1028232	chr6:26005449-26319756	Flanking Active TSS Genic enhancers Active TSS Bivalent/Poised TSS Weak transcription Enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	1171 gene(s)	inside rSNPs	diseases
15	nsv870314	chr6:26008435-26280807	Flanking Active TSS Enhancers Active TSS Genic enhancers Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	1151 gene(s)	inside rSNPs	diseases
16	nsv1023457	chr6:26014014-26305407	Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1170 gene(s)	inside rSNPs	diseases
17	nsv1025493	chr6:26026870-26223838	Weak transcription Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1001 gene(s)	inside rSNPs	diseases
18	nsv1023979	chr6:26026870-26287399	Flanking Active TSS Enhancers Bivalent/Poised TSS Active TSS Weak transcription Transcr. at gene 5' and 3' Strong transcription Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1113 gene(s)	inside rSNPs	diseases
19	nsv1015782	chr6:26026870-26323895	Active TSS Weak transcription Flanking Active TSS Enhancers Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1114 gene(s)	inside rSNPs	diseases
20	nsv1018665	chr6:26026870-26352046	Flanking Active TSS Weak transcription Active TSS Enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1116 gene(s)	inside rSNPs	diseases
21	nsv1026692	chr6:26027408-26067081	Flanking Active TSS Active TSS Enhancers Weak transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	363 gene(s)	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs9379821	U91328.19	cis	Adipose Subcutaneous	GTEx
rs9379821	U91328.19	cis	Muscle Skeletal	GTEx

Chromatin state (count:108 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:26044600-26054800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr6:26044600-26055000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr6:26045800-26054600	Weak transcription	Ovary	ovary
4	chr6:26046200-26054600	Weak transcription	Esophagus	oesophagus
5	chr6:26046800-26054400	Weak transcription	Placenta Amnion	Placenta Amnion
6	chr6:26048200-26054400	Weak transcription	Placenta	Placenta
7	chr6:26049200-26054400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr6:26052400-26054400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
9	chr6:26052400-26054600	Enhancers	Stomach Mucosa	stomach
10	chr6:26052600-26054400	Weak transcription	HUES64 Cell Line	embryonic stem cell
11	chr6:26052600-26054400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
12	chr6:26052800-26055200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr6:26053000-26054400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
14	chr6:26053200-26057400	Active TSS	K562	blood
15	chr6:26053600-26054400	Enhancers	Fetal Intestine Small	intestine
16	chr6:26053600-26055000	Flanking Active TSS	Fetal Thymus	thymus
17	chr6:26053600-26057200	Active TSS	Thymus	Thymus
18	chr6:26053800-26054400	Enhancers	Primary T cells fromperipheralblood	blood
19	chr6:26053800-26054400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
20	chr6:26053800-26054400	Enhancers	Primary T helper cells fromperipheralblood	blood
21	chr6:26053800-26054600	Enhancers	Primary neutrophils fromperipheralblood	blood
22	chr6:26053800-26054600	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
23	chr6:26053800-26054600	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
24	chr6:26053800-26054600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
25	chr6:26053800-26054800	Enhancers	Small Intestine	intestine
26	chr6:26054000-26054400	Enhancers	Primary T regulatory cells fromperipheralblood	blood
27	chr6:26054000-26054400	Enhancers	Cortex derived primary cultured neurospheres	brain
28	chr6:26054000-26054400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
29	chr6:26054000-26054400	Enhancers	Fetal Stomach	stomach
30	chr6:26054000-26054600	Enhancers	Primary B cells from peripheral blood	blood
31	chr6:26054000-26057400	Active TSS	GM12878-XiMat	blood
32	chr6:26054200-26054400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
33	chr6:26054200-26054400	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
34	chr6:26054200-26054400	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
35	chr6:26054200-26054400	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
36	chr6:26054200-26054400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
37	chr6:26054200-26054400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
38	chr6:26054200-26054400	Enhancers	Primary T helper naive cells from peripheral blood	blood
39	chr6:26054200-26054400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
40	chr6:26054200-26054400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
41	chr6:26054200-26054400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
42	chr6:26054200-26054400	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
43	chr6:26054200-26054400	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
44	chr6:26054200-26054400	Active TSS	Primary mononuclear cells fromperipheralblood	Blood
45	chr6:26054200-26054400	Enhancers	Brain Angular Gyrus	brain
46	chr6:26054200-26054400	Enhancers	Brain Cingulate Gyrus	brain
47	chr6:26054200-26054400	Enhancers	Brain Hippocampus Middle	brain
48	chr6:26054200-26054400	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
49	chr6:26054200-26054400	Active TSS	Brain Substantia Nigra	brain
50	chr6:26054200-26054400	Active TSS	Fetal Brain Male	brain

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