Variant report

Variant	rs5744607
Chromosome Location	chr5:74849029-74849030
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr5:74845037..74847535-chr5:74848930..74850561,2	K562	blood:

Extended variants
information (count: 18 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:6)

rs_ID	r²[population]
rs1820647	1.00[CEU][hapmap]
rs3097154	1.00[CEU][hapmap];1.00[GIH][hapmap]
rs3889900	1.00[CEU][hapmap];1.00[GIH][hapmap]
rs5744590	1.00[CEU][hapmap]
rs5744614	1.00[CEU][hapmap]
rs5744690	1.00[CEU][hapmap]

Variant overlapped rSNPs/rCNVs (count:12 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv882193	chr5:74656175-74917862	ZNF genes & repeats Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
2	nsv882194	chr5:74656175-74946455	Strong transcription Genic enhancers Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
3	nsv882195	chr5:74678937-74896798	Weak transcription Enhancers ZNF genes & repeats Active TSS Strong transcription Genic enhancers Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
4	nsv882196	chr5:74678937-74917862	Weak transcription Enhancers Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
5	nsv882197	chr5:74692776-74946455	Enhancers Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
6	nsv882198	chr5:74736065-74896798	Strong transcription Enhancers ZNF genes & repeats Active TSS Weak transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
7	nsv882199	chr5:74757758-74946455	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Strong transcription 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 miRNA target site	13 gene(s)	inside rSNPs	diseases
8	nsv1027368	chr5:74759999-75663712	Active TSS Strong transcription Flanking Active TSS Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
9	nsv882201	chr5:74787310-74890618	Weak transcription Flanking Active TSS Genic enhancers Strong transcription Enhancers ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region miRNA target site	11 gene(s)	inside rSNPs	diseases
10	nsv882202	chr5:74808417-74946455	Strong transcription Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
11	nsv882204	chr5:74811497-74856142	Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
12	nsv882205	chr5:74811497-74862921	Weak transcription ZNF genes & repeats Enhancers Strong transcription Genic enhancers Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:115 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:74808800-74849600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
2	chr5:74810400-74862400	Weak transcription	Hela-S3	cervix
3	chr5:74818200-74897400	Weak transcription	Thymus	Thymus
4	chr5:74822800-74896000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
5	chr5:74826000-74862400	Weak transcription	Fetal Heart	heart
6	chr5:74831000-74852600	Weak transcription	Aorta	Aorta
7	chr5:74831000-74859000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
8	chr5:74831000-74862400	Weak transcription	Rectal Smooth Muscle	rectum
9	chr5:74831200-74877200	Weak transcription	Fetal Kidney	kidney
10	chr5:74831800-74849200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
11	chr5:74832400-74859000	Weak transcription	Brain Angular Gyrus	brain
12	chr5:74832800-74861400	Weak transcription	Gastric	stomach
13	chr5:74833000-74849400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
14	chr5:74833000-74855400	Weak transcription	Esophagus	oesophagus
15	chr5:74833000-74860600	Weak transcription	A549	lung
16	chr5:74833000-74861600	Weak transcription	Spleen	Spleen
17	chr5:74833200-74862600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
18	chr5:74833400-74850000	Weak transcription	Left Ventricle	heart
19	chr5:74833400-74850400	Weak transcription	Stomach Smooth Muscle	stomach
20	chr5:74833400-74851000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
21	chr5:74833400-74852600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
22	chr5:74833400-74861600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
23	chr5:74833400-74861600	Weak transcription	Pancreas	Pancrea
24	chr5:74833400-74862000	Weak transcription	Lung	lung
25	chr5:74833400-74906800	Weak transcription	Brain Substantia Nigra	brain
26	chr5:74834600-74862400	Weak transcription	Small Intestine	intestine
27	chr5:74837600-74874400	Weak transcription	Fetal Brain Male	brain
28	chr5:74839400-74897400	Weak transcription	Sigmoid Colon	Sigmoid Colon
29	chr5:74840000-74849600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
30	chr5:74840200-74850400	Weak transcription	Cortex derived primary cultured neurospheres	brain
31	chr5:74840400-74850800	Weak transcription	Fetal Stomach	stomach
32	chr5:74840400-74852600	Weak transcription	Fetal Intestine Small	intestine
33	chr5:74840400-74852800	Weak transcription	Rectal Mucosa Donor 29	rectum
34	chr5:74840400-74862400	Weak transcription	Ovary	ovary
35	chr5:74841000-74849600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
36	chr5:74841000-74853000	Weak transcription	Psoas Muscle	Psoas
37	chr5:74841200-74861800	Weak transcription	Right Ventricle	heart
38	chr5:74841200-74899400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
39	chr5:74841800-74861600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
40	chr5:74842200-74853400	Weak transcription	Brain Germinal Matrix	brain
41	chr5:74843600-74850800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
42	chr5:74844600-74853000	Weak transcription	Brain Anterior Caudate	brain
43	chr5:74845200-74854800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
44	chr5:74845800-74852200	Strong transcription	Primary T helper cells fromperipheralblood	blood
45	chr5:74846000-74852200	Strong transcription	Primary T cells from cord blood	blood
46	chr5:74846200-74853200	Weak transcription	HUES6 Cell Line	embryonic stem cell
47	chr5:74846200-74865400	Weak transcription	Colonic Mucosa	Colon
48	chr5:74846600-74850400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
49	chr5:74847200-74852400	Strong transcription	Monocytes-CD14+_RO01746	blood
50	chr5:74847200-74852800	Weak transcription	Fetal Brain Female	brain

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