Variant report

Variant	rs3095426
Chromosome Location	chr6:139759591-139759592
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 11 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs1019237	0.83[CEU][hapmap];0.93[CHB][hapmap];0.85[CHD][hapmap];0.83[JPT][hapmap];0.93[LWK][hapmap];0.94[MEX][hapmap];0.92[TSI][hapmap];0.89[YRI][hapmap];0.87[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2005734	0.82[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2908495	0.83[CEU][hapmap];0.89[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs2908496	1.00[ASW][hapmap];0.90[CEU][hapmap];0.93[GIH][hapmap];0.84[LWK][hapmap];0.82[MEX][hapmap];0.92[TSI][hapmap];0.87[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs2908499	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs2908510	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs3010304	0.85[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs3010308	0.81[CEU][hapmap]
rs3010312	0.94[CEU][hapmap];0.85[AFR][1000 genomes];0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs3010316	0.83[CEU][hapmap];0.93[CHB][hapmap];0.83[JPT][hapmap];0.89[YRI][hapmap];0.85[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs887780	0.84[EUR][1000 genomes];0.89[ASN][1000 genomes]

No data

Chromatin state (count:15 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:139755000-139760000	Weak transcription	Primary hematopoietic stem cells	blood
2	chr6:139755200-139759600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr6:139755200-139760400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
4	chr6:139755400-139759600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
5	chr6:139755400-139764600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
6	chr6:139755600-139760600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
7	chr6:139755600-139763200	Weak transcription	Primary neutrophils fromperipheralblood	blood
8	chr6:139756000-139760400	Weak transcription	K562	blood
9	chr6:139757800-139760400	Weak transcription	Fetal Stomach	stomach
10	chr6:139758200-139760000	Enhancers	Fetal Heart	heart
11	chr6:139758200-139764200	Weak transcription	Fetal Kidney	kidney
12	chr6:139758400-139759600	Weak transcription	Colon Smooth Muscle	Colon
13	chr6:139758400-139759600	Weak transcription	Pancreas	Pancrea
14	chr6:139758400-139763400	Weak transcription	Placenta	Placenta
15	chr6:139758400-139764600	Weak transcription	Cortex derived primary cultured neurospheres	brain

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Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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