Variant report

Variant	rs10206966
Chromosome Location	chr2:30487388-30487389
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr2:30452974..30456196-chr2:30487344..30491801,6	K562	blood:
2	chr2:30486455..30489826-chr2:30493226..30495888,3	K562	blood:
3	chr2:30486354..30489346-chr2:30498547..30500363,2	K562	blood:

Variant related genes	Relation type
ENSG00000213626	Chromatin interaction

Extended variants
information (count: 6 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:3)

rs_ID	r²[population]
rs12714304	1.00[YRI][hapmap]
rs13388013	0.81[AFR][1000 genomes]
rs13409562	1.00[YRI][hapmap];0.90[AFR][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	nsv533886	chr2:30130019-31068764	ZNF genes & repeats Enhancers Genic enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
2	nsv1002657	chr2:30339312-30516535	Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Enhancers Active TSS Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
3	nsv2662	chr2:30462905-30495134	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:58 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:30476600-30496000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr2:30477000-30488800	Weak transcription	Primary hematopoietic stem cells	blood
3	chr2:30477800-30489000	Weak transcription	Stomach Mucosa	stomach
4	chr2:30478000-30488400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
5	chr2:30478200-30488400	Weak transcription	Right Atrium	heart
6	chr2:30478600-30487400	Weak transcription	K562	blood
7	chr2:30479200-30489000	Weak transcription	Rectal Mucosa Donor 31	rectum
8	chr2:30481000-30489400	Weak transcription	Small Intestine	intestine
9	chr2:30481400-30489800	Weak transcription	HUES64 Cell Line	embryonic stem cell
10	chr2:30481600-30489200	Weak transcription	H1 Cell Line	embryonic stem cell
11	chr2:30482000-30489600	Weak transcription	HUES48 Cell Line	embryonic stem cell
12	chr2:30482200-30488400	Weak transcription	Muscle Satellite Cultured Cells	--
13	chr2:30482200-30489000	Weak transcription	Rectal Smooth Muscle	rectum
14	chr2:30482200-30489400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr2:30482400-30488400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
16	chr2:30482400-30489000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
17	chr2:30482400-30489000	Weak transcription	Pancreas	Pancrea
18	chr2:30482400-30489000	Weak transcription	Sigmoid Colon	Sigmoid Colon
19	chr2:30482400-30491400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
20	chr2:30482600-30488400	Weak transcription	Lung	lung
21	chr2:30482600-30489000	Weak transcription	Esophagus	oesophagus
22	chr2:30482600-30489000	Weak transcription	Placenta	Placenta
23	chr2:30482800-30488400	Weak transcription	NH-A	brain
24	chr2:30482800-30489000	Weak transcription	Aorta	Aorta
25	chr2:30483200-30488400	Weak transcription	Left Ventricle	heart
26	chr2:30483200-30488800	Weak transcription	Fetal Heart	heart
27	chr2:30483400-30487400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
28	chr2:30483400-30487400	Weak transcription	Colon Smooth Muscle	Colon
29	chr2:30483400-30487600	Enhancers	Primary T helper cells fromperipheralblood	blood
30	chr2:30483400-30488400	Weak transcription	Osteobl	bone
31	chr2:30483400-30488800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
32	chr2:30483600-30489000	Weak transcription	Duodenum Smooth Muscle	Duodenum
33	chr2:30483800-30488400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
34	chr2:30483800-30488400	Weak transcription	Thymus	Thymus
35	chr2:30484000-30488000	Weak transcription	Primary B cells from cord blood	blood
36	chr2:30484000-30488400	Weak transcription	HSMM	muscle
37	chr2:30484000-30488400	Weak transcription	HSMMtube	muscle
38	chr2:30484000-30488400	Weak transcription	NHDF-Ad	bronchial
39	chr2:30484000-30488400	Weak transcription	NHLF	lung
40	chr2:30484000-30488800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
41	chr2:30485000-30487400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
42	chr2:30485000-30488400	Enhancers	Primary T cells fromperipheralblood	blood
43	chr2:30485600-30488400	Weak transcription	A549	lung
44	chr2:30485800-30488400	Enhancers	Primary T helper cells PMA-I stimulated	--
45	chr2:30486800-30488400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
46	chr2:30486800-30488400	Enhancers	Primary T killer memory cells from peripheral blood	blood
47	chr2:30487000-30487400	Enhancers	Fetal Thymus	thymus
48	chr2:30487000-30487600	Enhancers	Spleen	Spleen
49	chr2:30487000-30487800	Enhancers	Fetal Intestine Large	intestine
50	chr2:30487000-30488200	Enhancers	Primary T cells from cord blood	blood

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