Variant report

Variant	rs11674659
Chromosome Location	chr2:11636428-11636429
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr2:11631289..11634219-chr2:11636050..11638651,2	K562	blood:
2	chr2:11268242..11270233-chr2:11636174..11639118,2	MCF-7	breast:
3	chr2:11634128..11636998-chr2:11655433..11657027,2	K562	blood:

Extended variants
information (count: 21 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs10169987	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs10205078	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs11886420	1.00[AMR][1000 genomes]
rs11897533	1.00[AMR][1000 genomes]
rs12165170	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs13388093	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs13395155	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs13407457	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs13430148	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1595018	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AMR][1000 genomes]
rs16857565	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs2043542	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap]
rs2082829	1.00[AMR][1000 genomes]
rs2082830	1.00[AMR][1000 genomes]
rs4233893	1.00[AMR][1000 genomes]
rs4668729	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs6432202	1.00[CHB][hapmap]
rs6719003	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap]
rs6719009	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1010506	chr2:11430965-12057286	Enhancers Strong transcription Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	88 gene(s)	inside rSNPs	diseases
2	nsv535585	chr2:11430965-12057286	Enhancers Flanking Active TSS Bivalent/Poised TSS Weak transcription ZNF genes & repeats Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	88 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:45 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:11624000-11638600	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr2:11629000-11638600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
3	chr2:11632400-11638600	Weak transcription	Psoas Muscle	Psoas
4	chr2:11633000-11638400	Weak transcription	Skeletal Muscle Male	skeletal muscle
5	chr2:11633200-11638800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr2:11635000-11636600	Genic enhancers	HepG2	liver
7	chr2:11635800-11636600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
8	chr2:11635800-11636600	Enhancers	H1 Cell Line	embryonic stem cell
9	chr2:11635800-11636600	Enhancers	Cortex derived primary cultured neurospheres	brain
10	chr2:11635800-11636600	Active TSS	Brain Anterior Caudate	brain
11	chr2:11635800-11636600	Active TSS	Brain Hippocampus Middle	brain
12	chr2:11635800-11636600	Active TSS	Brain Inferior Temporal Lobe	brain
13	chr2:11635800-11636600	Active TSS	Brain Substantia Nigra	brain
14	chr2:11635800-11636600	Flanking Active TSS	Fetal Adrenal Gland	Adrenal Gland
15	chr2:11636000-11636600	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr2:11636000-11636600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
17	chr2:11636000-11636600	Active TSS	Brain Cingulate Gyrus	brain
18	chr2:11636000-11636600	Enhancers	Fetal Lung	lung
19	chr2:11636000-11636600	Flanking Active TSS	Ovary	ovary
20	chr2:11636000-11636600	Active TSS	Right Ventricle	heart
21	chr2:11636200-11636600	Flanking Active TSS	Brain Angular Gyrus	brain
22	chr2:11636200-11637400	Weak transcription	Fetal Heart	heart
23	chr2:11636200-11637800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
24	chr2:11636200-11638200	Weak transcription	HUES64 Cell Line	embryonic stem cell
25	chr2:11636200-11638600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr2:11636200-11638600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
27	chr2:11636400-11636600	Active TSS	ES-I3 Cell Line	embryonic stem cell
28	chr2:11636400-11636600	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
29	chr2:11636400-11636600	Active TSS	iPS-20b Cell Line	embryonic stem cell
30	chr2:11636400-11636600	Active TSS	Left Ventricle	heart
31	chr2:11636400-11637400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
32	chr2:11636400-11637800	Weak transcription	HUES6 Cell Line	embryonic stem cell
33	chr2:11636400-11637800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
34	chr2:11636400-11638600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr2:11636400-11638600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
36	chr2:11636400-11638600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
37	chr2:11636400-11638600	Weak transcription	Fetal Muscle Leg	muscle
38	chr2:11636400-11638600	Weak transcription	Lung	lung
39	chr2:11636400-11638600	Weak transcription	Pancreas	Pancrea
40	chr2:11636400-11638600	Weak transcription	Spleen	Spleen
41	chr2:11636400-11638800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
42	chr2:11636400-11639000	Weak transcription	HUES48 Cell Line	embryonic stem cell
43	chr2:11636400-11639000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
44	chr2:11636400-11639200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
45	chr2:11636400-11646400	Weak transcription	Right Atrium	heart

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