Variant report

Variant	rs4714744
Chromosome Location	chr6:44075844-44075845
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr6:44074659..44076273-chr6:44081817..44083659,2	MCF-7	breast:
2	chr6:44068030..44072338-chr6:44074661..44078042,4	K562	blood:
3	chr6:44075555..44078062-chr6:44223665..44227802,3	K562	blood:
4	chr6:44072850..44074417-chr6:44075167..44077237,2	MCF-7	breast:
5	chr6:44073239..44076204-chr6:44215001..44217094,2	K562	blood:
6	chr6:44060224..44061946-chr6:44074240..44078220,3	K562	blood:

Variant related genes	Relation type
ENSG00000096384	Chromatin interaction
ENSG00000157593	Chromatin interaction

Extended variants
information (count: 30 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs10428726	0.96[ASN][1000 genomes]
rs10807295	0.96[ASN][1000 genomes]
rs10948122	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10948123	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10948125	0.96[ASN][1000 genomes]
rs10948126	0.96[ASN][1000 genomes]
rs11966587	0.91[AFR][1000 genomes];0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11967633	0.96[ASN][1000 genomes]
rs11968386	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12525049	0.87[AFR][1000 genomes];0.97[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs12526662	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12664793	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2096200	0.96[ASN][1000 genomes]
rs35738079	0.81[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs41282654	0.93[ASN][1000 genomes]
rs4711765	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4714749	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55862642	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59028814	0.88[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60245793	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60691447	0.89[AFR][1000 genomes];0.93[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6912142	0.81[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs700006	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs713050	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73733834	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7738970	0.96[ASN][1000 genomes]
rs7771710	0.89[AFR][1000 genomes];0.93[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv931987	chr6:43624625-44350167	Enhancers Flanking Bivalent TSS/Enh Weak transcription Genic enhancers Bivalent Enhancer Flanking Active TSS Strong transcription Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	201 gene(s)	inside rSNPs	diseases
2	nsv462935	chr6:44046143-44117607	Enhancers Strong transcription Weak transcription Flanking Active TSS Bivalent/Poised TSS Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
3	nsv603002	chr6:44046143-44117607	Genic enhancers Weak transcription Strong transcription Flanking Active TSS Enhancers Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:127 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:44055800-44076000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
2	chr6:44055800-44078800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
3	chr6:44056200-44078400	Weak transcription	Fetal Kidney	kidney
4	chr6:44058800-44093600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
5	chr6:44059600-44079000	Weak transcription	Small Intestine	intestine
6	chr6:44063200-44076000	Weak transcription	Colonic Mucosa	Colon
7	chr6:44064600-44077600	Weak transcription	Stomach Mucosa	stomach
8	chr6:44065400-44077200	Weak transcription	Rectal Smooth Muscle	rectum
9	chr6:44066000-44081400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
10	chr6:44066000-44091000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
11	chr6:44066400-44082200	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
12	chr6:44066800-44079400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
13	chr6:44067000-44077200	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
14	chr6:44067000-44084200	Strong transcription	Brain Germinal Matrix	brain
15	chr6:44067000-44084400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
16	chr6:44067200-44085000	Strong transcription	Dnd41	blood
17	chr6:44067600-44079600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
18	chr6:44068600-44077400	Strong transcription	Fetal Intestine Small	intestine
19	chr6:44069000-44078600	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
20	chr6:44070000-44083200	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
21	chr6:44070400-44084000	Strong transcription	HUES6 Cell Line	embryonic stem cell
22	chr6:44070600-44084000	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
23	chr6:44070800-44079600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
24	chr6:44070800-44084200	Strong transcription	Cortex derived primary cultured neurospheres	brain
25	chr6:44071000-44081600	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
26	chr6:44071000-44084600	Strong transcription	iPS-20b Cell Line	embryonic stem cell
27	chr6:44071200-44076400	Strong transcription	Placenta Amnion	Placenta Amnion
28	chr6:44071200-44077400	Strong transcription	Fetal Intestine Large	intestine
29	chr6:44071200-44080000	Strong transcription	Gastric	stomach
30	chr6:44071200-44083400	Strong transcription	Fetal Thymus	thymus
31	chr6:44071200-44084200	Strong transcription	Fetal Brain Female	brain
32	chr6:44071200-44084600	Strong transcription	HUES64 Cell Line	embryonic stem cell
33	chr6:44071200-44084600	Strong transcription	Monocytes-CD14+_RO01746	blood
34	chr6:44071200-44086400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr6:44071400-44076600	Strong transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr6:44071400-44078000	Strong transcription	Duodenum Mucosa	Duodenum
37	chr6:44071400-44082200	Strong transcription	Primary B cells from cord blood	blood
38	chr6:44071400-44083800	Strong transcription	iPS-18 Cell Line	embryonic stem cell
39	chr6:44071400-44083800	Strong transcription	Primary T cells from cord blood	blood
40	chr6:44071400-44084400	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr6:44071400-44084400	Strong transcription	Primary monocytes fromperipheralblood	blood
42	chr6:44071600-44081800	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
43	chr6:44071600-44083200	Strong transcription	K562	blood
44	chr6:44071600-44084000	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
45	chr6:44071600-44084200	Strong transcription	HUES48 Cell Line	embryonic stem cell
46	chr6:44071600-44084400	Strong transcription	GM12878-XiMat	blood
47	chr6:44071800-44083600	Strong transcription	Primary T cells fromperipheralblood	blood
48	chr6:44071800-44084000	Strong transcription	H1 Cell Line	embryonic stem cell
49	chr6:44071800-44084400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
50	chr6:44072200-44076000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links