Variant report

Variant	rs13242904
Chromosome Location	chr7:8098818-8098819
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:8007674..8009181-chr7:8097178..8098947,2	K562	blood:

Variant related genes	Relation type
ENSG00000106415	Chromatin interaction

Extended variants
information (count: 37 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:32)

rs_ID	r²[population]
rs13222222	1.00[CEU][hapmap];0.81[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs13223417	1.00[CEU][hapmap];1.00[YRI][hapmap];0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs13223995	1.00[CEU][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs13237185	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs13239966	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs13240739	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs13245917	1.00[CEU][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs34318095	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs34475980	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs34783749	1.00[EUR][1000 genomes]
rs34955320	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs35044198	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs35108922	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs35171936	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs35225784	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35240411	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs35394048	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs35572840	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35627160	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs35630009	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs36015287	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs36022646	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs36028057	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs58769447	1.00[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs6969431	1.00[CEU][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs71533384	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs71533385	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs71533389	1.00[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs71533390	1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7800750	1.00[CEU][hapmap];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs7801299	1.00[CEU][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7807433	0.83[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2752177	chr7:7729247-8177689	Weak transcription Enhancers Transcr. at gene 5' and 3' Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
2	nsv917172	chr7:7854632-8807385	Weak transcription Flanking Active TSS Enhancers Strong transcription Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	56 gene(s)	inside rSNPs	diseases
3	nsv519058	chr7:8094604-8115794	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	nsv1020686	chr7:8095118-8311985	Enhancers Strong transcription Flanking Active TSS Weak transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
5	nsv538723	chr7:8095118-8311985	Weak transcription Strong transcription Enhancers Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:109 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:8043000-8099200	Weak transcription	Colon Smooth Muscle	Colon
2	chr7:8047600-8108200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
3	chr7:8065000-8108600	Weak transcription	H9 Cell Line	embryonic stem cell
4	chr7:8066400-8127600	Weak transcription	Rectal Smooth Muscle	rectum
5	chr7:8066600-8099800	Weak transcription	Rectal Mucosa Donor 29	rectum
6	chr7:8066600-8126000	Weak transcription	Rectal Mucosa Donor 31	rectum
7	chr7:8066800-8099800	Weak transcription	Brain Anterior Caudate	brain
8	chr7:8066800-8108600	Weak transcription	Brain Cingulate Gyrus	brain
9	chr7:8067000-8135400	Weak transcription	Pancreas	Pancrea
10	chr7:8075000-8108600	Weak transcription	Psoas Muscle	Psoas
11	chr7:8075000-8125800	Weak transcription	Lung	lung
12	chr7:8075000-8126800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
13	chr7:8075600-8101400	Weak transcription	K562	blood
14	chr7:8075600-8104400	Weak transcription	HMEC	breast
15	chr7:8075600-8105000	Weak transcription	HUES6 Cell Line	embryonic stem cell
16	chr7:8075600-8113000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr7:8075600-8131800	Weak transcription	Sigmoid Colon	Sigmoid Colon
18	chr7:8076000-8111800	Weak transcription	Fetal Brain Male	brain
19	chr7:8076000-8124200	Weak transcription	Fetal Kidney	kidney
20	chr7:8076200-8102200	Weak transcription	Fetal Brain Female	brain
21	chr7:8076200-8108400	Weak transcription	Brain Angular Gyrus	brain
22	chr7:8077200-8103200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
23	chr7:8077200-8106800	Weak transcription	Fetal Heart	heart
24	chr7:8084400-8103200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
25	chr7:8085200-8109000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr7:8085200-8128400	Weak transcription	Small Intestine	intestine
27	chr7:8088200-8099800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
28	chr7:8088600-8104400	Weak transcription	NH-A	brain
29	chr7:8088600-8108400	Weak transcription	Brain Substantia Nigra	brain
30	chr7:8088600-8108600	Weak transcription	Skeletal Muscle Male	skeletal muscle
31	chr7:8090400-8103200	Weak transcription	Muscle Satellite Cultured Cells	--
32	chr7:8091200-8101400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
33	chr7:8091400-8099600	Weak transcription	Primary T cells from cord blood	blood
34	chr7:8091400-8105000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
35	chr7:8091400-8127800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
36	chr7:8091800-8105000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
37	chr7:8092000-8103200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
38	chr7:8092000-8105000	Weak transcription	HUES48 Cell Line	embryonic stem cell
39	chr7:8092000-8108600	Weak transcription	Right Ventricle	heart
40	chr7:8092400-8108600	Weak transcription	H1 Cell Line	embryonic stem cell
41	chr7:8092600-8108600	Weak transcription	Right Atrium	heart
42	chr7:8093800-8100400	Weak transcription	Colonic Mucosa	Colon
43	chr7:8094000-8127800	Weak transcription	HSMM	muscle
44	chr7:8094400-8102200	Strong transcription	Dnd41	blood
45	chr7:8094400-8102800	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
46	chr7:8094600-8102600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
47	chr7:8094800-8102000	Strong transcription	Cortex derived primary cultured neurospheres	brain
48	chr7:8095000-8100800	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
49	chr7:8095000-8101600	Strong transcription	GM12878-XiMat	blood
50	chr7:8095000-8102000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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