Variant report

Variant	rs10844790
Chromosome Location	chr12:9937526-9937527
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:8)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:9936591..9939111-chr12:9947051..9948836,2	K562	blood:
2	chr12:9928036..9930338-chr12:9937118..9939542,2	K562	blood:
3	chr12:9930340..9931876-chr12:9935375..9937594,2	K562	blood:
4	chr12:9912416..9914377-chr12:9936821..9938730,2	K562	blood:
5	chr12:9906322..9908011-chr12:9937316..9939333,2	K562	blood:
6	chr12:9935876..9938398-chr12:9943768..9945628,3	K562	blood:
7	chr12:9901100..9927208-chr12:9932356..9954328,123	K562	blood:
8	chr12:9936898..9938906-chr12:9943638..9945628,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000110848	Chromatin interaction

Extended variants
information (count: 14 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs10772137	0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10772138	0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10844769	0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11053043	0.85[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1861090	0.80[ASN][1000 genomes]
rs2098299	0.85[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2110449	0.85[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2110450	0.85[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2110451	0.80[ASN][1000 genomes]
rs2110452	0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2160087	0.85[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7958591	0.85[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7976639	0.83[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7978977	0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]

No data

Chromatin state (count:21 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:9927600-9938800	Weak transcription	H1 Cell Line	embryonic stem cell
2	chr12:9928400-9945400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr12:9930000-9945400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
4	chr12:9930200-9945800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
5	chr12:9934400-9938400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
6	chr12:9934600-9937600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
7	chr12:9934600-9938200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
8	chr12:9934600-9939800	Weak transcription	Primary T cells from cord blood	blood
9	chr12:9934600-9940000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
10	chr12:9935200-9941200	Enhancers	iPS-15b Cell Line	embryonic stem cell
11	chr12:9935400-9938000	Weak transcription	Primary T helper cells fromperipheralblood	blood
12	chr12:9935400-9940400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
13	chr12:9936000-9941000	Enhancers	iPS-18 Cell Line	embryonic stem cell
14	chr12:9936800-9937800	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
15	chr12:9937000-9937600	Active TSS	ES-I3 Cell Line	embryonic stem cell
16	chr12:9937200-9937800	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
17	chr12:9937200-9940600	Enhancers	HUES64 Cell Line	embryonic stem cell
18	chr12:9937400-9937600	Enhancers	iPS-20b Cell Line	embryonic stem cell
19	chr12:9937400-9937600	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
20	chr12:9937400-9939000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
21	chr12:9937400-9939800	Enhancers	Primary T helper cells PMA-I stimulated	--

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