Variant report

Variant	rs9447543
Chromosome Location	chr6:76469353-76469354
allele	C/T
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:8)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:76467679..76469997-chr6:76472807..76474955,2	K562	blood:
2	chr6:76461303..76463860-chr6:76468925..76471220,2	K562	blood:
3	chr6:76457614..76459414-chr6:76469003..76470756,2	K562	blood:
4	chr6:76467679..76470814-chr6:76472807..76475124,3	K562	blood:
5	chr6:76467657..76469847-chr6:76559756..76561654,2	MCF-7	breast:
6	chr6:76457754..76460582-chr6:76467683..76471676,6	MCF-7	breast:
7	chr6:76461153..76463947-chr6:76466842..76469998,3	MCF-7	breast:
8	chr6:76469142..76471151-chr6:76480358..76482124,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000196586	Chromatin interaction

Extended variants
information (count: 130 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:107)

rs_ID	r²[population]
rs11963710	0.97[ASN][1000 genomes]
rs11964201	0.93[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11965869	1.00[CEU][hapmap]
rs11967411	1.00[CHB][hapmap];0.96[CHD][hapmap];1.00[GIH][hapmap];0.92[JPT][hapmap];0.80[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11968058	1.00[CHB][hapmap];0.92[JPT][hapmap];0.80[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11968226	0.93[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11969264	0.89[CHB][hapmap];0.83[JPT][hapmap];0.93[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12660075	1.00[CHB][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs12660330	1.00[CHB][hapmap];0.92[JPT][hapmap];0.80[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12660493	0.93[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12661973	0.93[ASN][1000 genomes]
rs12662248	1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12662475	1.00[CHB][hapmap];1.00[JPT][hapmap];0.80[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12662565	0.93[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12662672	1.00[CHB][hapmap];0.96[CHD][hapmap];1.00[GIH][hapmap];0.92[JPT][hapmap];1.00[MEX][hapmap];0.93[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12662718	1.00[CHB][hapmap];0.96[CHD][hapmap];1.00[GIH][hapmap];0.92[JPT][hapmap];0.80[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12662824	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12662879	1.00[CHB][hapmap];0.92[JPT][hapmap];0.80[EUR][1000 genomes]
rs12663203	1.00[CHB][hapmap];0.92[JPT][hapmap];0.80[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12663535	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12664049	0.86[JPT][hapmap]
rs12664146	1.00[CHB][hapmap];1.00[JPT][hapmap];0.80[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs12664721	0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12664742	0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12665404	1.00[CHB][hapmap];0.92[JPT][hapmap];0.80[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs13205059	1.00[CHB][hapmap];0.92[JPT][hapmap];0.83[YRI][hapmap];0.93[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1498383	1.00[CEU][hapmap]
rs16879451	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs16886792	1.00[CEU][hapmap]
rs16886870	1.00[CEU][hapmap]
rs2273858	0.80[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2295937	1.00[CHB][hapmap];0.92[JPT][hapmap];0.80[EUR][1000 genomes]
rs3778009	1.00[CHB][hapmap];0.92[JPT][hapmap];0.80[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs3798436	1.00[CHB][hapmap];0.92[JPT][hapmap];0.80[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs3798445	1.00[CHB][hapmap];0.92[JPT][hapmap];0.90[ASN][1000 genomes]
rs3798450	1.00[CHB][hapmap];0.92[JPT][hapmap];0.93[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs3798451	0.87[ASW][hapmap];1.00[CHB][hapmap];0.96[CHD][hapmap];1.00[GIH][hapmap];0.92[JPT][hapmap];0.93[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs3798452	0.94[AFR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs3798453	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs3798456	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs3798457	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56251027	0.93[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs59710688	0.80[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs59964990	0.81[ASN][1000 genomes]
rs60360183	0.93[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs61620194	0.80[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs67182025	0.93[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs72654748	0.80[ASN][1000 genomes]
rs72654749	0.80[ASN][1000 genomes]
rs72654750	0.85[ASN][1000 genomes]
rs72654751	0.93[ASN][1000 genomes]
rs72654752	0.96[ASN][1000 genomes]
rs72654753	0.99[ASN][1000 genomes]
rs72654754	0.99[ASN][1000 genomes]
rs72654755	0.97[ASN][1000 genomes]
rs72654756	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72654757	0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs72654758	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72654759	0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs72654760	0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs72654761	0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs72654762	0.93[AFR][1000 genomes];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs72654763	0.81[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs72654764	0.93[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs72654765	0.93[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs72654766	0.93[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs72654767	0.93[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs72654769	0.81[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs72654770	0.93[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs72654771	0.80[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs72654772	0.80[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs72654773	0.80[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs72654774	0.80[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs72654775	0.80[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs72654776	0.80[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs72654777	0.80[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs72654778	0.80[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs72654779	0.80[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs72654780	0.80[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs72654781	0.80[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs72654783	0.80[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs72654784	0.80[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs72654785	0.80[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs72654786	0.80[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs72654787	0.80[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs72654788	0.80[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs72654789	0.80[EUR][1000 genomes]
rs72654790	0.80[EUR][1000 genomes]
rs72654791	0.80[EUR][1000 genomes]
rs72654792	0.80[EUR][1000 genomes]
rs72654793	0.80[EUR][1000 genomes]
rs72674543	0.80[EUR][1000 genomes]
rs72674544	0.80[EUR][1000 genomes]
rs72674546	0.80[EUR][1000 genomes]
rs73751021	0.80[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs73751022	0.80[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs73751024	0.80[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7761217	0.82[AFR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9443187	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9443191	1.00[CHB][hapmap];0.92[JPT][hapmap];0.86[YRI][hapmap];0.93[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9443192	1.00[CHB][hapmap];0.92[JPT][hapmap];0.93[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9447544	0.97[AFR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9447545	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9447546	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.87[AFR][1000 genomes];0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9447549	0.93[AFR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9447552	0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9447555	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:23 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1027915	chr6:75893542-76510113	Active TSS Enhancers Strong transcription Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	70 gene(s)	inside rSNPs	diseases
2	nsv538311	chr6:75893542-76510113	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Strong transcription 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 miRNA miRNA target site	70 gene(s)	inside rSNPs	diseases
3	nsv1022428	chr6:76023118-76575620	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	48 gene(s)	inside rSNPs	diseases
4	nsv538312	chr6:76023118-76575620	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Active TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	48 gene(s)	inside rSNPs	diseases
5	nsv1032245	chr6:76045537-76545703	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	47 gene(s)	inside rSNPs	diseases
6	nsv538313	chr6:76045537-76545703	Strong transcription Weak transcription Enhancers Active TSS Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	47 gene(s)	inside rSNPs	diseases
7	nsv1019328	chr6:76154751-76604197	Enhancers Weak transcription Strong transcription Active TSS Bivalent/Poised TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	44 gene(s)	inside rSNPs	diseases
8	nsv538314	chr6:76154751-76604197	Enhancers Strong transcription Active TSS Weak transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	44 gene(s)	inside rSNPs	diseases
9	nsv1023331	chr6:76238459-76482117	Strong transcription ZNF genes & repeats Active TSS Weak transcription Flanking Active TSS Enhancers 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	38 gene(s)	inside rSNPs	diseases
10	nsv538315	chr6:76238459-76482117	Enhancers Strong transcription Flanking Active TSS Weak transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	38 gene(s)	inside rSNPs	diseases
11	nsv1017542	chr6:76238459-76537447	Strong transcription Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	38 gene(s)	inside rSNPs	diseases
12	nsv1031745	chr6:76257913-76493355	Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Strong transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	38 gene(s)	inside rSNPs	diseases
13	nsv538316	chr6:76257913-76493355	Strong transcription Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	38 gene(s)	inside rSNPs	diseases
14	nsv533100	chr6:76257914-76493354	Enhancers Weak transcription Strong transcription Genic enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	38 gene(s)	inside rSNPs	diseases
15	nsv1023749	chr6:76287578-76482117	Weak transcription Flanking Active TSS Genic enhancers Strong transcription Enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	38 gene(s)	inside rSNPs	diseases
16	nsv538317	chr6:76287578-76482117	Strong transcription Weak transcription Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	38 gene(s)	inside rSNPs	diseases
17	nsv1021090	chr6:76306100-76759397	Weak transcription Enhancers Active TSS Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
18	nsv538318	chr6:76306100-76759397	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Bivalent/Poised TSS Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
19	nsv886185	chr6:76320846-76498109	Weak transcription Strong transcription Flanking Active TSS Enhancers ZNF genes & repeats Active TSS Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
20	nsv1032961	chr6:76343575-76788852	Strong transcription Weak transcription Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
21	nsv932201	chr6:76365548-77219650	Enhancers Weak transcription Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
22	nsv1028340	chr6:76410921-76960225	Flanking Bivalent TSS/Enh Strong transcription Weak transcription Enhancers Active TSS Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
23	nsv538319	chr6:76410921-76960225	Strong transcription Weak transcription Enhancers Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:46 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:76459600-76472200	Weak transcription	Small Intestine	intestine
2	chr6:76460000-76475600	Weak transcription	Psoas Muscle	Psoas
3	chr6:76460000-76481400	Weak transcription	Aorta	Aorta
4	chr6:76460600-76476800	Weak transcription	Lung	lung
5	chr6:76461000-76480800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr6:76461000-76485000	Weak transcription	Fetal Stomach	stomach
7	chr6:76461400-76475000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr6:76461600-76470200	Weak transcription	Duodenum Mucosa	Duodenum
9	chr6:76461600-76475800	Weak transcription	Rectal Mucosa Donor 31	rectum
10	chr6:76461600-76485000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr6:76462400-76482200	Weak transcription	Cortex derived primary cultured neurospheres	brain
12	chr6:76463000-76470200	Weak transcription	Brain Angular Gyrus	brain
13	chr6:76463400-76470600	Weak transcription	Fetal Intestine Large	intestine
14	chr6:76463400-76485200	Weak transcription	Gastric	stomach
15	chr6:76463600-76470200	Weak transcription	Brain Cingulate Gyrus	brain
16	chr6:76463600-76470400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
17	chr6:76463600-76476000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
18	chr6:76463800-76473800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
19	chr6:76463800-76478400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
20	chr6:76464000-76470200	Weak transcription	HSMMtube	muscle
21	chr6:76464200-76478800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
22	chr6:76464200-76481600	Weak transcription	HUVEC	blood vessel
23	chr6:76464200-76485000	Weak transcription	Pancreas	Pancrea
24	chr6:76466000-76469600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
25	chr6:76466200-76471400	Weak transcription	Fetal Intestine Small	intestine
26	chr6:76467400-76471600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
27	chr6:76467400-76471800	Weak transcription	Sigmoid Colon	Sigmoid Colon
28	chr6:76469000-76469400	Enhancers	Primary hematopoietic stem cells	blood
29	chr6:76469000-76469400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
30	chr6:76469000-76469400	Enhancers	Fetal Kidney	kidney
31	chr6:76469000-76469400	Enhancers	Left Ventricle	heart
32	chr6:76469000-76469400	Enhancers	GM12878-XiMat	blood
33	chr6:76469000-76469400	Enhancers	Osteobl	bone
34	chr6:76469000-76469600	Enhancers	iPS-18 Cell Line	embryonic stem cell
35	chr6:76469000-76470000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
36	chr6:76469000-76470200	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
37	chr6:76469000-76470800	Enhancers	Breast Myoepithelial Primary Cells	Breast
38	chr6:76469000-76470800	Enhancers	Brain Hippocampus Middle	brain
39	chr6:76469000-76471000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
40	chr6:76469000-76471000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
41	chr6:76469000-76471000	Enhancers	Brain Inferior Temporal Lobe	brain
42	chr6:76469000-76471400	Enhancers	Brain Anterior Caudate	brain
43	chr6:76469000-76471400	Enhancers	Brain Substantia Nigra	brain
44	chr6:76469200-76469400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
45	chr6:76469200-76470000	Weak transcription	HSMM	muscle
46	chr6:76469200-76471200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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