Variant report

Variant	rs6747765
Chromosome Location	chr2:153304996-153304997
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr2:153191085..153193954-chr2:153302933..153305841,2	MCF-7	breast:
2	chr2:153297043..153301991-chr2:153303133..153306232,4	K562	blood:
3	chr2:153301457..153305742-chr2:153308329..153310586,3	K562	blood:

Variant related genes	Relation type
ENSG00000157827	Chromatin interaction

Extended variants
information (count: 38 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:33)

rs_ID	r²[population]
rs10173899	0.81[CHB][hapmap];0.94[JPT][hapmap]
rs10179418	1.00[ASW][hapmap];0.89[CEU][hapmap];1.00[CHB][hapmap];0.97[CHD][hapmap];0.93[GIH][hapmap];1.00[JPT][hapmap];0.82[LWK][hapmap];0.83[MEX][hapmap];0.95[MKK][hapmap];0.95[TSI][hapmap];0.88[YRI][hapmap];0.87[AFR][1000 genomes];0.81[AMR][1000 genomes];0.86[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10194603	0.88[CHB][hapmap];0.94[JPT][hapmap]
rs10208776	0.94[CHB][hapmap];0.94[JPT][hapmap];0.82[ASN][1000 genomes]
rs10432493	1.00[CHB][hapmap];0.94[JPT][hapmap];0.86[ASN][1000 genomes]
rs11674872	0.82[JPT][hapmap]
rs12693378	0.94[JPT][hapmap]
rs13011152	0.86[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs13386403	0.87[JPT][hapmap]
rs13390698	0.87[CHB][hapmap];1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs13424038	0.94[CHB][hapmap];0.94[JPT][hapmap];0.81[ASN][1000 genomes]
rs13427076	0.82[CHB][hapmap];1.00[JPT][hapmap];0.82[ASN][1000 genomes]
rs16831169	0.88[CHB][hapmap];0.94[JPT][hapmap]
rs16831174	0.88[CHB][hapmap];0.94[JPT][hapmap]
rs2078444	0.88[AMR][1000 genomes];0.86[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2346205	0.81[CHB][hapmap];0.94[JPT][hapmap]
rs2346209	0.89[CEU][hapmap];0.88[CHB][hapmap];0.88[GIH][hapmap];0.94[JPT][hapmap];0.82[MEX][hapmap];0.81[TSI][hapmap];0.87[AMR][1000 genomes]
rs2881339	0.89[CEU][hapmap];0.88[CHB][hapmap];0.88[GIH][hapmap];0.94[JPT][hapmap];0.81[AMR][1000 genomes]
rs4143274	0.89[CEU][hapmap];0.88[CHB][hapmap];0.94[JPT][hapmap]
rs4146259	0.82[CHD][hapmap];0.88[JPT][hapmap]
rs4664587	1.00[CEU][hapmap];0.87[CHB][hapmap];0.94[JPT][hapmap];0.81[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs58121347	0.81[ASN][1000 genomes]
rs6434059	0.94[JPT][hapmap]
rs6713348	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6725661	0.81[CHB][hapmap];0.94[JPT][hapmap]
rs6737699	0.94[CHB][hapmap];1.00[JPT][hapmap];0.89[ASN][1000 genomes]
rs6748954	0.94[CHB][hapmap];0.94[JPT][hapmap];0.81[ASN][1000 genomes]
rs73002264	0.91[ASN][1000 genomes]
rs7559217	0.88[CHB][hapmap];0.94[JPT][hapmap]
rs7582984	0.93[JPT][hapmap]
rs7586195	0.94[JPT][hapmap]
rs7587794	0.94[CHB][hapmap];0.94[JPT][hapmap];0.81[ASN][1000 genomes]
rs7606592	0.82[CHB][hapmap];0.85[CHD][hapmap];0.82[GIH][hapmap];0.94[JPT][hapmap];0.83[ASN][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	nsv834419	chr2:153179420-153381476	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
2	esv3693436	chr2:153219836-153479857	Weak transcription Active TSS Enhancers Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
3	nsv875291	chr2:153251742-153339823	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
4	nsv1013777	chr2:153273637-153538546	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
5	esv2754362	chr2:153297577-153366129	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:66 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:153280000-153305200	Enhancers	Brain Cingulate Gyrus	brain
2	chr2:153286400-153305200	Enhancers	Brain Substantia Nigra	brain
3	chr2:153291600-153305200	Weak transcription	H9 Cell Line	embryonic stem cell
4	chr2:153295400-153308600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr2:153295400-153311000	Weak transcription	Ovary	ovary
6	chr2:153295800-153305200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr2:153297000-153305600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
8	chr2:153298800-153308800	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
9	chr2:153299000-153305200	Enhancers	Brain Angular Gyrus	brain
10	chr2:153299800-153305200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
11	chr2:153300200-153305200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
12	chr2:153300400-153305800	Enhancers	Adipose Nuclei	Adipose
13	chr2:153300600-153307000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
14	chr2:153300600-153311200	Weak transcription	Lung	lung
15	chr2:153300800-153306600	Enhancers	HepG2	liver
16	chr2:153301000-153314200	Weak transcription	Placenta	Placenta
17	chr2:153301200-153305200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
18	chr2:153301400-153305200	Enhancers	HMEC	breast
19	chr2:153301600-153307200	Weak transcription	H1 Cell Line	embryonic stem cell
20	chr2:153301600-153311200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
21	chr2:153301800-153306200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
22	chr2:153301800-153307200	Weak transcription	Fetal Thymus	thymus
23	chr2:153301800-153321000	Weak transcription	Right Atrium	heart
24	chr2:153302000-153305200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
25	chr2:153302400-153305800	Enhancers	NHEK	skin
26	chr2:153302400-153312400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
27	chr2:153302400-153321600	Weak transcription	Left Ventricle	heart
28	chr2:153302600-153309200	Weak transcription	Skeletal Muscle Female	skeletal muscle
29	chr2:153302600-153309800	Weak transcription	Fetal Stomach	stomach
30	chr2:153302800-153305000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
31	chr2:153302800-153305800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
32	chr2:153302800-153311200	Weak transcription	Colon Smooth Muscle	Colon
33	chr2:153302800-153314800	Weak transcription	Aorta	Aorta
34	chr2:153303000-153305200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
35	chr2:153303000-153305200	Enhancers	Brain Inferior Temporal Lobe	brain
36	chr2:153303000-153305400	Enhancers	Brain Hippocampus Middle	brain
37	chr2:153303000-153305600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
38	chr2:153303000-153312600	Weak transcription	Hela-S3	cervix
39	chr2:153303200-153305200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
40	chr2:153303200-153306800	Weak transcription	Fetal Brain Male	brain
41	chr2:153303200-153309200	Weak transcription	A549	lung
42	chr2:153303400-153305400	Weak transcription	Fetal Lung	lung
43	chr2:153303400-153305800	Weak transcription	Duodenum Smooth Muscle	Duodenum
44	chr2:153303400-153306000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr2:153303400-153307200	Weak transcription	Fetal Brain Female	brain
46	chr2:153303400-153308400	Weak transcription	NH-A	brain
47	chr2:153303400-153311200	Weak transcription	Skeletal Muscle Male	skeletal muscle
48	chr2:153303400-153322600	Weak transcription	NHLF	lung
49	chr2:153303600-153311000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
50	chr2:153303600-153312000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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