Variant report

Variant	rs1721858
Chromosome Location	chr7:121603637-121603638
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 34 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:34)

rs_ID	r²[population]
rs11767822	0.84[EUR][1000 genomes]
rs1196477	0.97[ASN][1000 genomes]
rs1196478	0.84[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1196480	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs1196481	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs1196483	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs1196484	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs1196486	0.82[EUR][1000 genomes]
rs1196487	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs1196488	0.89[AFR][1000 genomes];0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1196490	0.83[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs1196491	0.89[AFR][1000 genomes];0.90[AMR][1000 genomes];0.92[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1196493	0.91[AFR][1000 genomes];0.94[AMR][1000 genomes];0.92[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1196494	0.91[AFR][1000 genomes];0.94[AMR][1000 genomes];0.92[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1196495	0.91[AFR][1000 genomes];0.93[AMR][1000 genomes];0.92[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1196496	0.83[AFR][1000 genomes];0.94[AMR][1000 genomes];0.88[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1196510	0.81[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs1196511	0.97[AMR][1000 genomes];0.91[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1211621	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs12671846	0.83[EUR][1000 genomes]
rs1721857	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1721859	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs1916875	0.83[EUR][1000 genomes]
rs1916876	0.87[AFR][1000 genomes];0.89[AMR][1000 genomes];0.93[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2024252	0.83[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs2690271	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2690272	0.82[AFR][1000 genomes];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4629793	0.84[EUR][1000 genomes]
rs4731044	0.83[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs6961716	0.83[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs6967270	0.83[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs727766	0.83[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs7794741	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs7810556	0.84[AMR][1000 genomes]

No data

Chromatin state (count:25 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:121582600-121617600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
2	chr7:121592000-121609600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr7:121596000-121618400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr7:121601600-121606000	Weak transcription	Fetal Brain Male	brain
5	chr7:121601600-121628000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
6	chr7:121601800-121604800	Weak transcription	H9 Cell Line	embryonic stem cell
7	chr7:121601800-121607200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr7:121601800-121625600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
9	chr7:121602000-121605200	Weak transcription	HUES6 Cell Line	embryonic stem cell
10	chr7:121602000-121614600	Weak transcription	Fetal Brain Female	brain
11	chr7:121602400-121618200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
12	chr7:121602600-121605600	Weak transcription	Brain Germinal Matrix	brain
13	chr7:121603200-121603800	Genic enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
14	chr7:121603200-121604000	Enhancers	H1 Cell Line	embryonic stem cell
15	chr7:121603200-121604000	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
16	chr7:121603200-121604000	Enhancers	Cortex derived primary cultured neurospheres	brain
17	chr7:121603200-121604600	Genic enhancers	HUES64 Cell Line	embryonic stem cell
18	chr7:121603200-121605000	Enhancers	iPS-15b Cell Line	embryonic stem cell
19	chr7:121603400-121603800	Genic enhancers	ES-I3 Cell Line	embryonic stem cell
20	chr7:121603400-121603800	Enhancers	iPS-20b Cell Line	embryonic stem cell
21	chr7:121603400-121604000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
22	chr7:121603400-121604200	Enhancers	HUES48 Cell Line	embryonic stem cell
23	chr7:121603400-121631400	Weak transcription	NHEK	skin
24	chr7:121603600-121604600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
25	chr7:121603600-121614800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin

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