Variant report

Variant	rs624411
Chromosome Location	chr1:75156077-75156078
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr1:75118268..75118957-chr1:75155576..75156140,2	MCF-7	breast:
2	chr1:75117987..75118877-chr1:75155539..75156443,2	MCF-7	breast:
3	chr1:75154629..75156914-chr1:75162681..75164412,2	K562	blood:

Extended variants
information (count: 17 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs516819	0.84[AMR][1000 genomes]
rs696119	0.82[CEU][hapmap]
rs696666	1.00[ASN][1000 genomes]
rs696667	1.00[ASN][1000 genomes]
rs696668	1.00[ASN][1000 genomes]
rs696669	1.00[ASN][1000 genomes]
rs696672	1.00[ASN][1000 genomes]
rs696703	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs699800	1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1011745	chr1:74730942-75477618	Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
2	nsv535003	chr1:74730942-75477618	Flanking Active TSS Active TSS Weak transcription Enhancers Strong transcription Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
3	nsv830259	chr1:75089177-75241062	Weak transcription Flanking Active TSS ZNF genes & repeats Enhancers Active TSS Strong transcription Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
4	nsv461995	chr1:75133142-75166623	Enhancers Bivalent/Poised TSS Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
5	nsv546578	chr1:75133142-75166623	Flanking Bivalent TSS/Enh Enhancers Weak transcription Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
6	esv2762153	chr1:75142205-75171211	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
7	nsv871152	chr1:75152186-75197533	Weak transcription Flanking Active TSS Genic enhancers Strong transcription Enhancers ZNF genes & repeats Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	n/a
8	esv1851105	chr1:75152186-75302921	Enhancers Strong transcription Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:23 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:75141800-75179600	Weak transcription	Aorta	Aorta
2	chr1:75154600-75156200	Enhancers	Cortex derived primary cultured neurospheres	brain
3	chr1:75154600-75156200	Enhancers	Fetal Brain Male	brain
4	chr1:75155200-75156200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr1:75155200-75156200	Enhancers	Ovary	ovary
6	chr1:75155400-75156200	Enhancers	Fetal Lung	lung
7	chr1:75155400-75156400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr1:75155600-75156200	Enhancers	HUVEC	blood vessel
9	chr1:75155600-75156600	Enhancers	ES-I3 Cell Line	embryonic stem cell
10	chr1:75155600-75159200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
11	chr1:75155800-75156200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr1:75155800-75156200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr1:75155800-75156200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
14	chr1:75155800-75156200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
15	chr1:75155800-75156200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr1:75155800-75156200	Enhancers	HepG2	liver
17	chr1:75155800-75156400	Enhancers	HUES48 Cell Line	embryonic stem cell
18	chr1:75155800-75156400	Enhancers	HUES6 Cell Line	embryonic stem cell
19	chr1:75156000-75156200	Enhancers	GM12878-XiMat	blood
20	chr1:75156000-75158000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
21	chr1:75156000-75158800	Weak transcription	NH-A	brain
22	chr1:75156000-75167600	Weak transcription	Liver	Liver
23	chr1:75156000-75183400	Weak transcription	Fetal Heart	heart

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