Variant report

Variant	rs273996
Chromosome Location	chr7:137630775-137630776
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:137621450..137623446-chr7:137630610..137633140,2	K562	blood:
2	chr7:137620440..137622660-chr7:137629916..137631573,2	MCF-7	breast:

Extended variants
information (count: 29 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:26)

rs_ID	r²[population]
rs10275270	0.84[GIH][hapmap]
rs110595	0.85[ASN][1000 genomes]
rs112417	0.96[CEU][hapmap];1.00[CHB][hapmap];0.88[JPT][hapmap];0.85[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12534066	0.84[GIH][hapmap]
rs273973	0.89[AMR][1000 genomes];0.91[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs273974	0.83[AMR][1000 genomes];0.90[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs273976	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs273977	1.00[CEU][hapmap];1.00[CHB][hapmap];0.88[JPT][hapmap];0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs273979	0.93[CHB][hapmap];0.82[JPT][hapmap];0.85[ASN][1000 genomes]
rs273980	0.93[CHB][hapmap];0.82[JPT][hapmap];0.85[ASN][1000 genomes]
rs273981	0.96[CEU][hapmap];1.00[CHB][hapmap];0.89[CHD][hapmap];0.98[GIH][hapmap];0.88[JPT][hapmap];1.00[MEX][hapmap];0.85[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs273984	0.96[CEU][hapmap];1.00[CHB][hapmap];0.88[JPT][hapmap];0.88[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs273986	0.89[ASN][1000 genomes]
rs273987	0.93[CHB][hapmap];0.82[JPT][hapmap];0.89[ASN][1000 genomes]
rs273988	1.00[CEU][hapmap];1.00[CHB][hapmap];0.81[CHD][hapmap];0.88[JPT][hapmap];0.82[MEX][hapmap];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs273989	0.96[CEU][hapmap];1.00[CHB][hapmap];0.89[CHD][hapmap];1.00[GIH][hapmap];0.88[JPT][hapmap];1.00[MEX][hapmap];0.88[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs273990	0.96[CEU][hapmap];1.00[CHB][hapmap];0.88[JPT][hapmap];0.86[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs273991	1.00[CEU][hapmap];1.00[CHB][hapmap];0.87[JPT][hapmap];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs273992	0.93[CHB][hapmap];0.82[JPT][hapmap];0.89[ASN][1000 genomes]
rs273995	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.89[CHD][hapmap];0.93[GIH][hapmap];0.88[JPT][hapmap];1.00[LWK][hapmap];0.95[MEX][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs274001	0.85[CHB][hapmap]
rs274002	1.00[CEU][hapmap];0.93[CHB][hapmap];0.91[GIH][hapmap];0.91[MEX][hapmap];0.80[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs274003	0.89[CEU][hapmap];0.86[CHB][hapmap];0.82[JPT][hapmap];0.81[ASN][1000 genomes]
rs274004	0.85[CEU][hapmap];0.86[CHB][hapmap];0.81[ASN][1000 genomes]
rs274007	0.85[CEU][hapmap];0.93[GIH][hapmap]
rs7795277	0.84[EUR][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	nsv831150	chr7:137500559-137652808	Enhancers Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Strong transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
2	nsv518070	chr7:137534627-137808839	Enhancers Flanking Active TSS Weak transcription Strong transcription Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
3	esv3331245	chr7:137630762-137632760	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:95 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:137615600-137635600	Weak transcription	Hela-S3	cervix
2	chr7:137618200-137637200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
3	chr7:137621200-137638000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr7:137621400-137651800	Weak transcription	Primary T cells fromperipheralblood	blood
5	chr7:137621800-137633800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
6	chr7:137622000-137643000	Weak transcription	Primary monocytes fromperipheralblood	blood
7	chr7:137622200-137636600	Weak transcription	Esophagus	oesophagus
8	chr7:137622200-137638200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr7:137622200-137643200	Weak transcription	Monocytes-CD14+_RO01746	blood
10	chr7:137622400-137638400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
11	chr7:137624200-137633400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
12	chr7:137625800-137637200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
13	chr7:137625800-137638200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
14	chr7:137626000-137632800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr7:137626000-137637000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr7:137626000-137637000	Weak transcription	NHEK	skin
17	chr7:137626000-137646200	Weak transcription	HMEC	breast
18	chr7:137626400-137630800	Weak transcription	Gastric	stomach
19	chr7:137626400-137631800	Weak transcription	Lung	lung
20	chr7:137626400-137637000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
21	chr7:137626400-137637400	Weak transcription	Fetal Muscle Trunk	muscle
22	chr7:137626800-137631400	Enhancers	Stomach Smooth Muscle	stomach
23	chr7:137627400-137638200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
24	chr7:137627800-137630800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
25	chr7:137627800-137632200	Weak transcription	Right Ventricle	heart
26	chr7:137628200-137632200	Weak transcription	Sigmoid Colon	Sigmoid Colon
27	chr7:137628200-137637800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
28	chr7:137628400-137635200	Weak transcription	GM12878-XiMat	blood
29	chr7:137628600-137631200	Genic enhancers	K562	blood
30	chr7:137628600-137632600	Weak transcription	Right Atrium	heart
31	chr7:137628600-137633800	Weak transcription	Left Ventricle	heart
32	chr7:137628600-137637200	Weak transcription	Colonic Mucosa	Colon
33	chr7:137628800-137632600	Weak transcription	Psoas Muscle	Psoas
34	chr7:137628800-137636400	Weak transcription	Ovary	ovary
35	chr7:137628800-137636600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
36	chr7:137628800-137638600	Weak transcription	HUVEC	blood vessel
37	chr7:137629000-137630800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
38	chr7:137629000-137631800	Weak transcription	Small Intestine	intestine
39	chr7:137629000-137633200	Weak transcription	Fetal Heart	heart
40	chr7:137629000-137633600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
41	chr7:137629000-137634800	Weak transcription	Placenta Amnion	Placenta Amnion
42	chr7:137629000-137638000	Weak transcription	Adipose Nuclei	Adipose
43	chr7:137629200-137631400	Enhancers	Brain Hippocampus Middle	brain
44	chr7:137629200-137631800	Weak transcription	Stomach Mucosa	stomach
45	chr7:137629200-137632600	Weak transcription	Rectal Mucosa Donor 31	rectum
46	chr7:137629200-137632600	Weak transcription	A549	lung
47	chr7:137629200-137633000	Weak transcription	Duodenum Smooth Muscle	Duodenum
48	chr7:137629200-137633400	Weak transcription	H9 Cell Line	embryonic stem cell
49	chr7:137629200-137633600	Weak transcription	Skeletal Muscle Female	skeletal muscle
50	chr7:137629200-137634600	Weak transcription	Primary B cells from cord blood	blood

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