Variant report

Variant	rs17036311
Chromosome Location	chr2:47385059-47385060
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:24)
CpG islands
(count:0)
Chromatin interactive
region (count:4)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:24 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr2:47382524-47406811	PFSK-1	brain:	n/a	n/a
2	POLR2A	chr2:47384997-47385280	GM12891	blood:	n/a	n/a
3	POLR2A	chr2:47382225-47405286	PFSK-1	brain:	n/a	n/a
4	POLR2A	chr2:47383854-47385244	SK-N-SH	brain:	n/a	n/a
5	POLR2A	chr2:47384935-47385063	MCF10A-Er-Src	breast:	n/a	n/a
6	POLR2A	chr2:47382104-47386243	MCF-7	breast:	n/a	n/a
7	POLR2A	chr2:47384514-47385348	HUVEC	blood vessel:	n/a	n/a
8	POLR2A	chr2:47382411-47391126	SK-N-SH	brain:	n/a	n/a
9	POLR2A	chr2:47382450-47387588	PANC-1	pancreas:	n/a	n/a
10	POLR2A	chr2:47383789-47385251	Hela-S3	cervix:	n/a	n/a
11	POLR2A	chr2:47382708-47385289	U87	brain:	n/a	n/a
12	POLR2A	chr2:47384558-47385222	HUVEC	blood vessel:	n/a	n/a
13	POLR2A	chr2:47382692-47385176	GM12891	blood:	n/a	n/a
14	POLR2A	chr2:47382595-47387178	PANC-1	pancreas:	n/a	n/a
15	POLR2A	chr2:47382208-47387634	U87	brain:	n/a	n/a
16	POLR2A	chr2:47384626-47386313	HepG2	liver:	n/a	n/a
17	BCL3	chr2:47382628-47385203	A549	lung:	n/a	chr2:47384658-47384667
18	POLR2A	chr2:47382271-47387210	U87	brain:	n/a	n/a
19	POLR2A	chr2:47385044-47386328	GM12892	blood:	n/a	n/a
20	POLR2A	chr2:47383767-47385124	HUVEC	blood vessel:	n/a	n/a
21	POLR2A	chr2:47383059-47391091	K562	blood:	n/a	n/a
22	POLR2A	chr2:47382601-47385060	GM12878	blood:	n/a	n/a
23	POLR2A	chr2:47384459-47385244	HepG2	liver:	n/a	n/a
24	STAT3	chr2:47385056-47385122	MCF10A-Er-Src	breast:	n/a	n/a

No data

(count:4 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:47384081..47386449-chr2:47504881..47507810,2	K562	blood:
2	chr2:47381115..47385095-chr2:47400722..47404896,4	MCF-7	breast:
3	chr2:47383453..47385887-chr2:47388520..47390045,2	MCF-7	breast:
4	chr2:47383557..47385169-chr2:47392127..47393923,2	MCF-7	breast:

No data

Variant related genes	Relation type
C2orf61	TF binding region
ENSG00000143933	Chromatin interaction

Extended variants
information (count: 30 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:26)

rs_ID	r²[population]
rs11842	0.82[AMR][1000 genomes]
rs1693888	0.85[ASN][1000 genomes]
rs1693889	0.85[ASN][1000 genomes]
rs17036300	0.91[ASW][hapmap];1.00[CEU][hapmap];0.82[GIH][hapmap];0.94[LWK][hapmap];0.94[MEX][hapmap];0.91[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];0.94[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs17036313	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.85[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17036316	0.83[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.97[LWK][hapmap];1.00[MEX][hapmap];0.94[MKK][hapmap];1.00[TSI][hapmap];0.96[YRI][hapmap];0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17036320	0.91[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.91[GIH][hapmap];1.00[JPT][hapmap];0.87[LWK][hapmap];1.00[MEX][hapmap];0.94[TSI][hapmap];1.00[YRI][hapmap];0.92[AFR][1000 genomes];0.96[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17036325	1.00[CEU][hapmap];0.82[CHB][hapmap];0.90[YRI][hapmap];0.96[AMR][1000 genomes];0.91[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1723485	0.85[ASN][1000 genomes]
rs2347617	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4953469	1.00[CEU][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes];0.98[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs4953470	0.91[ASW][hapmap];1.00[CEU][hapmap];0.85[GIH][hapmap];1.00[LWK][hapmap];0.94[MEX][hapmap];0.91[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];0.98[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs4953471	1.00[CEU][hapmap];0.95[YRI][hapmap];0.88[AFR][1000 genomes];0.94[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs4953472	0.90[AMR][1000 genomes]
rs56875665	0.94[AMR][1000 genomes]
rs59415749	0.95[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6713257	0.96[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6749284	1.00[CEU][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];0.96[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs6760339	0.93[AFR][1000 genomes];0.98[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs72810414	0.97[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs72810415	0.95[AFR][1000 genomes];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs72810417	0.97[AFR][1000 genomes];0.98[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs72810419	0.96[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs72877054	0.92[AFR][1000 genomes];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7583684	0.87[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs815812	0.85[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv817517	chr2:46819371-47715140	Enhancers Weak transcription Genic enhancers Bivalent Enhancer Flanking Active TSS Strong transcription Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	152 gene(s)	inside rSNPs	diseases
2	nsv1004828	chr2:47056849-47814482	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	144 gene(s)	inside rSNPs	diseases
3	nsv457374	chr2:47313624-47448865	Enhancers Flanking Active TSS Weak transcription Genic enhancers Strong transcription Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	87 gene(s)	inside rSNPs	diseases
4	nsv581754	chr2:47313624-47448865	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	87 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:47357000-47385400	Weak transcription	Colon Smooth Muscle	Colon
2	chr2:47357000-47386600	Weak transcription	Fetal Heart	heart
3	chr2:47357000-47386800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr2:47357200-47386400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
5	chr2:47357400-47385400	Weak transcription	Fetal Intestine Large	intestine
6	chr2:47360600-47386800	Weak transcription	Stomach Mucosa	stomach
7	chr2:47363400-47386400	Weak transcription	Rectal Smooth Muscle	rectum
8	chr2:47366200-47397000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
9	chr2:47366800-47399400	Strong transcription	Fetal Thymus	thymus
10	chr2:47367000-47401200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
11	chr2:47367200-47402000	Weak transcription	Esophagus	oesophagus
12	chr2:47367600-47385400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
13	chr2:47367600-47386800	Weak transcription	Right Ventricle	heart
14	chr2:47367600-47387400	Weak transcription	Pancreas	Pancrea
15	chr2:47368800-47385200	Weak transcription	Fetal Intestine Small	intestine
16	chr2:47369000-47385600	Weak transcription	HUES64 Cell Line	embryonic stem cell
17	chr2:47369200-47386800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr2:47369600-47386200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
19	chr2:47369800-47386800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
20	chr2:47369800-47386800	Weak transcription	Psoas Muscle	Psoas
21	chr2:47369800-47391200	Strong transcription	Primary neutrophils fromperipheralblood	blood
22	chr2:47370000-47389600	Strong transcription	Muscle Satellite Cultured Cells	--
23	chr2:47371200-47385800	Weak transcription	Fetal Kidney	kidney
24	chr2:47371200-47388200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
25	chr2:47371400-47386600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
26	chr2:47371600-47389800	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
27	chr2:47371800-47392200	Strong transcription	Osteobl	bone
28	chr2:47372000-47386800	Weak transcription	H9 Cell Line	embryonic stem cell
29	chr2:47372600-47386800	Weak transcription	Gastric	stomach
30	chr2:47372600-47396800	Weak transcription	Small Intestine	intestine
31	chr2:47373600-47385400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
32	chr2:47374800-47385600	Weak transcription	HepG2	liver
33	chr2:47375400-47386000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
34	chr2:47375600-47397400	Weak transcription	Fetal Brain Male	brain
35	chr2:47376000-47388000	Strong transcription	HSMM	muscle
36	chr2:47376400-47389800	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
37	chr2:47377400-47385600	Weak transcription	Dnd41	blood
38	chr2:47377400-47386400	Weak transcription	Primary hematopoietic stem cells	blood
39	chr2:47377400-47386800	Weak transcription	Skeletal Muscle Male	skeletal muscle
40	chr2:47377600-47385400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
41	chr2:47377600-47385800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
42	chr2:47377600-47385800	Weak transcription	Skeletal Muscle Female	skeletal muscle
43	chr2:47377600-47386600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
44	chr2:47377600-47386800	Weak transcription	Colonic Mucosa	Colon
45	chr2:47377800-47385400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
46	chr2:47378200-47385600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
47	chr2:47378200-47386800	Weak transcription	K562	blood
48	chr2:47378400-47385600	Weak transcription	Rectal Mucosa Donor 29	rectum
49	chr2:47378400-47392000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
50	chr2:47378600-47385200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--

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