Variant report

Variant	rs11687510
Chromosome Location	chr2:98334679-98334680
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr2:98278882..98281534-chr2:98334105..98336255,2	K562	blood:
2	chr2:98323754..98326397-chr2:98334462..98336180,3	MCF-7	breast:
3	chr2:98334014..98335728-chr2:98339666..98342653,2	K562	blood:
4	chr12:7052555..7053181-chr2:98334664..98335205,2	NB4	blood:
5	chr2:98325414..98327155-chr2:98332598..98334979,2	K562	blood:

Variant related genes	Relation type
ENSG00000115085	Chromatin interaction
ENSG00000111678	Chromatin interaction
ENSG00000238923	Chromatin interaction
ENSG00000201806	Chromatin interaction
ENSG00000228486	Chromatin interaction
ENSG00000115073	Chromatin interaction

Extended variants
information (count: 42 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:37)

rs_ID	r²[population]
rs10460480	0.80[ASN][1000 genomes]
rs11678558	0.95[CEU][hapmap];0.88[EUR][1000 genomes]
rs11679828	0.87[CEU][hapmap];0.90[TSI][hapmap]
rs11686881	0.95[CEU][hapmap];0.80[GIH][hapmap];0.94[TSI][hapmap];0.88[EUR][1000 genomes]
rs11688829	0.87[CEU][hapmap]
rs11692470	0.87[CEU][hapmap]
rs12988571	0.87[CEU][hapmap];0.87[TSI][hapmap]
rs13023980	0.87[CEU][hapmap]
rs13033383	0.95[CEU][hapmap];0.80[GIH][hapmap];0.94[TSI][hapmap];0.81[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs17033906	1.00[CHB][hapmap];0.84[ASN][1000 genomes]
rs17488834	0.95[CEU][hapmap];0.89[EUR][1000 genomes]
rs17488897	0.87[CEU][hapmap]
rs17489454	0.87[CEU][hapmap];0.90[TSI][hapmap]
rs17490429	0.87[CEU][hapmap]
rs2278699	1.00[CHB][hapmap];0.84[ASN][1000 genomes]
rs2278700	0.87[CEU][hapmap];0.90[TSI][hapmap]
rs2289918	0.84[ASN][1000 genomes]
rs2289919	0.82[ASN][1000 genomes]
rs2305143	0.87[CEU][hapmap];0.90[TSI][hapmap]
rs3192177	0.95[CEU][hapmap];0.80[GIH][hapmap];0.94[TSI][hapmap];0.89[EUR][1000 genomes]
rs34149969	0.80[EUR][1000 genomes]
rs35321446	0.84[ASN][1000 genomes]
rs56293187	0.84[ASN][1000 genomes]
rs56948188	0.86[ASN][1000 genomes]
rs57831860	0.84[ASN][1000 genomes]
rs58511420	0.84[ASN][1000 genomes]
rs62157588	0.83[ASN][1000 genomes]
rs6543040	0.88[CHB][hapmap]
rs6711101	0.87[CEU][hapmap]
rs6711959	1.00[CHB][hapmap];0.83[CHD][hapmap];0.84[ASN][1000 genomes]
rs6738389	0.87[CEU][hapmap];0.87[TSI][hapmap]
rs72951160	0.84[ASN][1000 genomes]
rs73963109	0.84[ASN][1000 genomes]
rs746003	0.84[ASN][1000 genomes]
rs746004	0.84[ASN][1000 genomes]
rs7565744	1.00[CHB][hapmap];0.84[ASN][1000 genomes]
rs895438	0.87[CEU][hapmap];0.81[TSI][hapmap]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2757819	chr2:97571109-98336507	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	64 gene(s)	inside rSNPs	diseases
2	esv2759077	chr2:97571109-98336507	Flanking Active TSS Bivalent Enhancer Active TSS Genic enhancers Weak transcription Strong transcription Bivalent/Poised TSS Enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	64 gene(s)	inside rSNPs	diseases
3	nsv531382	chr2:98250628-98457616	Weak transcription Enhancers Active TSS Strong transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
4	nsv874696	chr2:98309882-98362907	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
5	esv33510	chr2:98317103-98341302	Enhancers Flanking Active TSS Genic enhancers Weak transcription Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:44 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:98329000-98336000	Enhancers	Fetal Muscle Leg	muscle
2	chr2:98330000-98337200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr2:98330200-98334800	Weak transcription	GM12878-XiMat	blood
4	chr2:98330200-98335800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
5	chr2:98330800-98336000	Transcr. at gene 5' and 3'	Fetal Thymus	thymus
6	chr2:98331200-98334800	Weak transcription	Primary B cells from cord blood	blood
7	chr2:98331200-98335000	Transcr. at gene 5' and 3'	Primary T cells fromperipheralblood	blood
8	chr2:98331200-98335800	Transcr. at gene 5' and 3'	Thymus	Thymus
9	chr2:98331200-98337200	Weak transcription	Sigmoid Colon	Sigmoid Colon
10	chr2:98331400-98336000	Flanking Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
11	chr2:98331400-98336200	Transcr. at gene 5' and 3'	Primary Natural Killer cells fromperipheralblood	blood
12	chr2:98331600-98336000	Flanking Active TSS	Primary T helper memory cells from peripheral blood 2	blood
13	chr2:98331800-98335800	Weak transcription	HUES6 Cell Line	embryonic stem cell
14	chr2:98332000-98336000	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
15	chr2:98332000-98340000	Weak transcription	Esophagus	oesophagus
16	chr2:98332400-98335800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
17	chr2:98332600-98335400	Active TSS	Rectal Mucosa Donor 29	rectum
18	chr2:98332600-98337200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr2:98332800-98335000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
20	chr2:98332800-98336000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
21	chr2:98333200-98336000	Flanking Active TSS	Primary T cells from cord blood	blood
22	chr2:98333200-98336000	Enhancers	Fetal Muscle Trunk	muscle
23	chr2:98333400-98336000	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
24	chr2:98333400-98336600	Enhancers	Primary hematopoietic stem cells short term culture	blood
25	chr2:98333400-98336600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
26	chr2:98333600-98334800	Weak transcription	Spleen	Spleen
27	chr2:98333600-98341800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
28	chr2:98334000-98334800	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
29	chr2:98334000-98334800	Enhancers	HSMMtube	muscle
30	chr2:98334000-98335200	Flanking Active TSS	Primary mononuclear cells fromperipheralblood	Blood
31	chr2:98334000-98336000	Transcr. at gene 5' and 3'	Dnd41	blood
32	chr2:98334200-98335800	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
33	chr2:98334200-98336200	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
34	chr2:98334200-98336600	Enhancers	Primary hematopoietic stem cells	blood
35	chr2:98334400-98335000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
36	chr2:98334400-98335000	Enhancers	Primary B cells from peripheral blood	blood
37	chr2:98334400-98336000	Flanking Active TSS	Primary T killer naive cells fromperipheralblood	blood
38	chr2:98334400-98336000	Active TSS	Colonic Mucosa	Colon
39	chr2:98334600-98334800	Active TSS	Primary T killer memory cells from peripheral blood	blood
40	chr2:98334600-98335800	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
41	chr2:98334600-98335800	Active TSS	Rectal Smooth Muscle	rectum
42	chr2:98334600-98336000	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
43	chr2:98334600-98336000	Active TSS	Duodenum Mucosa	Duodenum
44	chr2:98334600-98336200	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood

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