Variant report

Variant	rs34801978
Chromosome Location	chr17:46620688-46620689
allele	A/C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:106)
CpG islands
(count:0)
Chromatin interactive
region (count:1)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:106 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	YY1	chr17:46620288-46621103	GM12878	blood:	n/a	n/a
2	TAF1	chr17:46620173-46622395	K562	blood:	n/a	n/a
3	POLR2A	chr17:46620117-46628421	PANC-1	pancreas:	n/a	n/a
4	POLR2A	chr17:46618007-46622747	K562	blood:	n/a	n/a
5	RELA	chr17:46620573-46622055	GM15510	blood:	n/a	n/a
6	POU2F2	chr17:46620602-46621045	GM12878	blood:	n/a	n/a
7	MAX	chr17:46620244-46621443	A549	lung:	n/a	chr17:46621225-46621235
8	POLR2A	chr17:46616545-46629919	PANC-1	pancreas:	n/a	n/a
9	SUZ12	chr17:46620315-46621889	H1-hESC	embryonic stem cell:	n/a	n/a
10	POLR2A	chr17:46616973-46622292	K562	blood:	n/a	n/a
11	YY1	chr17:46620470-46621003	GM12892	blood:	n/a	n/a
12	POLR2A	chr17:46620418-46621441	GM12878	blood:	n/a	n/a
13	TBP	chr17:46620467-46621863	GM12878	blood:	n/a	n/a
14	POLR2A	chr17:46620588-46621673	K562	blood:	n/a	n/a
15	POLR2A	chr17:46620439-46621541	MCF10A-Er-Src	breast:	n/a	n/a
16	MAX	chr17:46620387-46621344	GM12878	blood:	n/a	chr17:46621225-46621235
17	UBTF	chr17:46618433-46622294	K562	blood:	n/a	n/a
18	POLR2A	chr17:46620459-46621196	A549	lung:	n/a	n/a
19	E2F6	chr17:46620297-46621086	A549	lung:	n/a	n/a
20	ZBTB7A	chr17:46620567-46621021	K562	blood:	n/a	n/a
21	TCF3	chr17:46620548-46620900	GM12878	blood:	n/a	n/a
22	POLR2A	chr17:46620513-46620764	MCF-7	breast:	n/a	n/a
23	POLR2A	chr17:46620344-46622195	GM18526	blood:	n/a	n/a
24	POLR2A	chr17:46620615-46620851	K562	blood:	n/a	n/a
25	POLR2A	chr17:46620424-46621205	A549	lung:	n/a	n/a
26	POLR2A	chr17:46620205-46621071	GM12878	blood:	n/a	n/a
27	POLR2A	chr17:46620263-46621110	GM12891	blood:	n/a	n/a
28	UBTF	chr17:46618409-46622293	K562	blood:	n/a	n/a
29	POLR2A	chr17:46620306-46622275	GM19193	blood:	n/a	n/a
30	YY1	chr17:46620541-46621247	K562	blood:	n/a	chr17:46621221-46621232 chr17:46621224-46621233
31	POLR2A	chr17:46620505-46621188	GM12878	blood:	n/a	n/a
32	POLR2A	chr17:46620403-46622760	K562	blood:	n/a	n/a
33	POLR2A	chr17:46620220-46622735	K562	blood:	n/a	n/a
34	EP300	chr17:46620586-46621204	GM12878	blood:	n/a	n/a
35	POLR2A	chr17:46620305-46622155	GM12878	blood:	n/a	n/a
36	POLR2A	chr17:46620385-46621565	GM12878	blood:	n/a	n/a
37	POLR2A	chr17:46620589-46620962	HUVEC	blood vessel:	n/a	n/a
38	ZBTB7A	chr17:46620569-46621056	K562	blood:	n/a	n/a
39	MAZ	chr17:46620510-46622186	GM12878	blood:	n/a	chr17:46621225-46621235
40	SIN3AK20	chr17:46620330-46621415	PANC-1	pancreas:	n/a	n/a
41	POLR2A	chr17:46620079-46622806	U87	brain:	n/a	n/a
42	FOXA2	chr17:46620497-46621345	A549	lung:	n/a	n/a
43	POLR2A	chr17:46620435-46621483	GM10847	blood:	n/a	n/a
44	POLR2A	chr17:46620315-46621225	GM12892	blood:	n/a	n/a
45	POLR2A	chr17:46620299-46626078	K562	blood:	n/a	n/a
46	POLR2A	chr17:46620207-46622131	U87	brain:	n/a	n/a
47	POLR2A	chr17:46618296-46623366	K562	blood:	n/a	n/a
48	GABPA	chr17:46620647-46621204	H1-hESC	embryonic stem cell:	n/a	n/a
49	POLR2A	chr17:46620231-46621255	GM12891	blood:	n/a	n/a
50	ZNF263	chr17:46620263-46621151	HEK293-T-REx	kidney:	n/a	n/a

No data

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr17:46618868..46624573-chr17:46700689..46705978,10	K562	blood:

No data

Variant related genes	Relation type
HOXB2	TF binding region
HOXB-AS1	TF binding region
ENSG00000170689	Chromatin interaction

Extended variants
information (count: 27 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:8)

rs_ID	r²[population]
rs16958023	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35114525	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs35384218	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs71369832	1.00[EUR][1000 genomes]
rs7208911	1.00[EUR][1000 genomes]
rs7213899	1.00[EUR][1000 genomes]
rs7215174	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73326060	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:19 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv833469	chr17:46491849-46709406	Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	349 gene(s)	inside rSNPs	diseases
2	esv3420538	chr17:46504944-46861553	Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	369 gene(s)	inside rSNPs	diseases
3	nsv908577	chr17:46584900-46704536	Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS Strong transcription Enhancers Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	343 gene(s)	inside rSNPs	diseases
4	nsv908578	chr17:46592413-46698710	Flanking Bivalent TSS/Enh Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	335 gene(s)	inside rSNPs	diseases
5	nsv908579	chr17:46592413-46727289	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Enhancers Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Strong transcription Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	349 gene(s)	inside rSNPs	diseases
6	nsv532113	chr17:46598247-47588570	Genic enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	453 gene(s)	inside rSNPs	diseases
7	esv2758459	chr17:46602673-46836837	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	364 gene(s)	inside rSNPs	diseases
8	esv2758694	chr17:46602673-46836837	Active TSS Bivalent Enhancer Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	364 gene(s)	inside rSNPs	diseases
9	nsv908580	chr17:46609103-46698710	Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers Enhancers Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Weak transcription Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	335 gene(s)	inside rSNPs	diseases
10	nsv908581	chr17:46610646-46735520	Bivalent Enhancer Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	349 gene(s)	inside rSNPs	diseases
11	nsv575480	chr17:46617019-46684929	Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Strong transcription Enhancers Weak transcription Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	322 gene(s)	inside rSNPs	diseases
12	nsv908582	chr17:46617019-46698710	Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Enhancers Genic enhancers Weak transcription Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	334 gene(s)	inside rSNPs	diseases
13	nsv908583	chr17:46617019-46704536	Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Weak transcription Strong transcription Genic enhancers Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	342 gene(s)	inside rSNPs	diseases
14	nsv833471	chr17:46617787-46783345	Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	356 gene(s)	inside rSNPs	diseases
15	nsv908584	chr17:46618926-46735520	Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	348 gene(s)	inside rSNPs	diseases
16	nsv457822	chr17:46620402-46698710	Flanking Active TSS Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3' Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Strong transcription Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	334 gene(s)	inside rSNPs	diseases
17	nsv575481	chr17:46620402-46698710	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription Transcr. at gene 5' and 3' Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	334 gene(s)	inside rSNPs	diseases
18	nsv457823	chr17:46620402-46704536	Enhancers Active TSS Bivalent Enhancer Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	342 gene(s)	inside rSNPs	diseases
19	nsv575482	chr17:46620402-46704536	Active TSS Flanking Bivalent TSS/Enh Weak transcription Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	342 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:114 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:46618200-46622400	Active TSS	Rectal Smooth Muscle	rectum
2	chr17:46618400-46621000	Transcr. at gene 5' and 3'	Fetal Stomach	stomach
3	chr17:46618400-46621600	Transcr. at gene 5' and 3'	IMR90 fetal lung fibroblasts Cell Line	lung
4	chr17:46618400-46622000	Bivalent/Poised TSS	Duodenum Mucosa	Duodenum
5	chr17:46618400-46622400	Bivalent/Poised TSS	Fetal Intestine Large	intestine
6	chr17:46618400-46622400	Bivalent/Poised TSS	Thymus	Thymus
7	chr17:46618400-46622600	Active TSS	Right Atrium	heart
8	chr17:46618400-46622600	Flanking Bivalent TSS/Enh	Monocytes-CD14+_RO01746	blood
9	chr17:46618600-46620800	Active TSS	Lung	lung
10	chr17:46618600-46620800	Bivalent/Poised TSS	Skeletal Muscle Female	skeletal muscle
11	chr17:46618600-46621200	Transcr. at gene 5' and 3'	NHLF	lung
12	chr17:46618600-46621400	Bivalent/Poised TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
13	chr17:46618600-46621400	Active TSS	Primary T helper naive cells from peripheral blood	blood
14	chr17:46618600-46622200	Active TSS	Esophagus	oesophagus
15	chr17:46618600-46622200	Bivalent/Poised TSS	GM12878-XiMat	blood
16	chr17:46618600-46622400	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
17	chr17:46618600-46622400	Active TSS	Aorta	Aorta
18	chr17:46618600-46622400	Active TSS	Placenta Amnion	Placenta Amnion
19	chr17:46618600-46622600	Bivalent/Poised TSS	ES-WA7 Cell Line	embryonic stem cell
20	chr17:46618600-46622600	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr17:46618600-46622600	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
22	chr17:46618600-46622600	Bivalent/Poised TSS	Fetal Lung	lung
23	chr17:46618800-46620800	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin02	Skin
24	chr17:46618800-46621200	Transcr. at gene 5' and 3'	Primary T helper 17 cells PMA-I stimulated	--
25	chr17:46618800-46621400	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
26	chr17:46618800-46621600	Active TSS	Primary T helper memory cells from peripheral blood 1	blood
27	chr17:46618800-46621800	Bivalent/Poised TSS	Left Ventricle	heart
28	chr17:46618800-46622000	Bivalent/Poised TSS	Pancreatic Islets	Pancreatic Islet
29	chr17:46618800-46622200	Active TSS	Primary T helper memory cells from peripheral blood 2	blood
30	chr17:46618800-46622600	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
31	chr17:46618800-46622600	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
32	chr17:46618800-46622600	Bivalent/Poised TSS	Duodenum Smooth Muscle	Duodenum
33	chr17:46618800-46622600	Active TSS	Fetal Kidney	kidney
34	chr17:46618800-46622600	Active TSS	K562	blood
35	chr17:46618800-46622600	Active TSS	NHDF-Ad	bronchial
36	chr17:46618800-46623000	Bivalent/Poised TSS	H9 Derived Neuron Cultured Cells	ES cell derived
37	chr17:46618800-46625600	Bivalent/Poised TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr17:46619000-46621200	Active TSS	Gastric	stomach
39	chr17:46619000-46622000	Active TSS	Sigmoid Colon	Sigmoid Colon
40	chr17:46619000-46622400	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
41	chr17:46619000-46622400	Active TSS	Primary T cells from cord blood	blood
42	chr17:46619000-46622400	Active TSS	Primary T killer naive cells fromperipheralblood	blood
43	chr17:46619000-46622400	Active TSS	Stomach Smooth Muscle	stomach
44	chr17:46619000-46622600	Active TSS	HMEC	breast
45	chr17:46619000-46622600	Active TSS	HSMM	muscle
46	chr17:46619000-46622600	Active TSS	HSMMtube	muscle
47	chr17:46619000-46622600	Bivalent/Poised TSS	Osteobl	bone
48	chr17:46619400-46620800	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
49	chr17:46619400-46621000	Transcr. at gene 5' and 3'	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
50	chr17:46619400-46621000	Transcr. at gene 5' and 3'	Muscle Satellite Cultured Cells	--

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