Variant report

Variant	rs233483
Chromosome Location	chr6:14815615-14815616
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:14814819..14819286-chr6:14819431..14823938,6	K562	blood:
2	chr6:14814509..14817952-chr6:14819306..14824906,6	K562	blood:

Extended variants
information (count: 35 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs11751114	0.93[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11970548	0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs16875778	0.88[ASN][1000 genomes]
rs16875782	0.88[ASN][1000 genomes]
rs2031298	0.88[ASN][1000 genomes]
rs233482	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs233484	0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs233485	0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs233486	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs233487	0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs233488	0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs233489	0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs233490	0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs233491	0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs233494	0.98[EUR][1000 genomes]
rs4537147	0.92[ASN][1000 genomes]
rs60681633	0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs62390273	0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs62390274	0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs62390275	0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs62390276	0.92[ASN][1000 genomes]
rs62390277	0.92[ASN][1000 genomes]
rs62390278	0.88[ASN][1000 genomes]
rs62390279	0.88[ASN][1000 genomes]
rs62390280	0.88[ASN][1000 genomes]
rs62390283	0.88[ASN][1000 genomes]
rs62390284	0.88[ASN][1000 genomes]
rs62390285	0.88[ASN][1000 genomes]
rs62390288	0.88[ASN][1000 genomes]
rs6927683	0.88[ASN][1000 genomes]
rs6939905	0.88[ASN][1000 genomes]
rs9476665	0.94[EUR][1000 genomes];0.92[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	nsv1023685	chr6:14514647-14838390	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
2	nsv1031668	chr6:14774036-15044308	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription Active TSS Strong transcription ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
3	nsv538138	chr6:14774036-15044308	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:14805400-14819000	Weak transcription	Right Atrium	heart
2	chr6:14806400-14818800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr6:14807600-14816200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
4	chr6:14809000-14824400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr6:14810800-14819000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr6:14810800-14823200	Weak transcription	H9 Cell Line	embryonic stem cell
7	chr6:14811600-14816600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
8	chr6:14812200-14816200	Weak transcription	Osteobl	bone
9	chr6:14812200-14824000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
10	chr6:14814200-14818000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr6:14814200-14822600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
12	chr6:14814400-14816600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr6:14815400-14815800	Active TSS	Colon Smooth Muscle	Colon
14	chr6:14815400-14816000	Enhancers	Small Intestine	intestine
15	chr6:14815400-14817000	Enhancers	HUES64 Cell Line	embryonic stem cell
16	chr6:14815400-14817600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
17	chr6:14815400-14818800	Enhancers	Brain Germinal Matrix	brain
18	chr6:14815400-14820000	Enhancers	Duodenum Mucosa	Duodenum
19	chr6:14815600-14816400	Enhancers	Breast Myoepithelial Primary Cells	Breast
20	chr6:14815600-14816800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
21	chr6:14815600-14817000	Enhancers	HUES48 Cell Line	embryonic stem cell
22	chr6:14815600-14817400	Enhancers	HUES6 Cell Line	embryonic stem cell
23	chr6:14815600-14817800	Enhancers	Cortex derived primary cultured neurospheres	brain
24	chr6:14815600-14818200	Enhancers	Fetal Intestine Small	intestine

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