Variant report

Variant	rs538308934
Chromosome Location	chr17:20901911-20901912
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:83)
CpG islands
(count:0)
Chromatin interactive
region (count:3)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:83 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	FOSL2	chr17:20899864-20904071	HepG2	liver:	n/a	chr17:20902795-20902805 chr17:20902795-20902805 chr17:20902795-20902805 chr17:20902204-20902216
2	POLR2A	chr17:20901604-20901912	HepG2	liver:	n/a	n/a
3	POLR2A	chr17:20899351-20909849	K562	blood:	n/a	n/a
4	POLR2A	chr17:20900490-20903179	K562	blood:	n/a	n/a
5	POLR2A	chr17:20901407-20902768	HL-60	blood:	n/a	n/a
6	POLR2A	chr17:20901052-20902950	GM12891	blood:	n/a	n/a
7	POLR2A	chr17:20899206-20903031	SK-N-SH	brain:	n/a	n/a
8	POLR2A	chr17:20900814-20902988	GM12878	blood:	n/a	n/a
9	NFATC1	chr17:20900906-20902881	GM12878	blood:	n/a	chr17:20902246-20902259
10	POLR2A	chr17:20900994-20903050	HepG2	liver:	n/a	n/a
11	POLR2A	chr17:20901226-20902882	Hela-S3	cervix:	n/a	n/a
12	POLR2A	chr17:20901746-20902276	Hela-S3	cervix:	n/a	n/a
13	POLR2A	chr17:20901121-20902989	HCT-116	colon:	n/a	n/a
14	POLR2A	chr17:20899538-20902748	U87	brain:	n/a	n/a
15	JUND	chr17:20900984-20902063	A549	lung:	n/a	n/a
16	POLR2A	chr17:20900597-20902264	PANC-1	pancreas:	n/a	n/a
17	POLR2A	chr17:20900827-20901962	A549	lung:	n/a	n/a
18	POLR2A	chr17:20900462-20902080	HepG2	liver:	n/a	n/a
19	SIN3AK20	chr17:20900728-20902534	SK-N-SH	brain:	n/a	n/a
20	POLR2A	chr17:20900886-20902025	GM19193	blood:	n/a	n/a
21	SIN3AK20	chr17:20901401-20902157	A549	lung:	n/a	n/a
22	POLR2A	chr17:20900826-20901956	A549	lung:	n/a	n/a
23	TCF12	chr17:20901171-20902143	A549	lung:	n/a	n/a
24	POLR2A	chr17:20900273-20901981	U87	brain:	n/a	n/a
25	POLR2A	chr17:20900718-20903554	H1-hESC	embryonic stem cell:	n/a	n/a
26	BCL3	chr17:20900503-20902569	A549	lung:	n/a	n/a
27	POLR2A	chr17:20900974-20902342	HUVEC	blood vessel:	n/a	n/a
28	MTA3	chr17:20900675-20902913	GM12878	blood:	n/a	n/a
29	POLR2A	chr17:20899537-20902909	ECC-1	luminal epithelium:	n/a	n/a
30	POLR2A	chr17:20901616-20902177	GM12878	blood:	n/a	n/a
31	BCL3	chr17:20901646-20902196	GM12878	blood:	n/a	n/a
32	POLR2A	chr17:20900921-20902164	GM12878	blood:	n/a	n/a
33	POLR2A	chr17:20901100-20902969	HL-60	blood:	n/a	n/a
34	POLR2A	chr17:20900596-20902478	HUVEC	blood vessel:	n/a	n/a
35	POLR2A	chr17:20899493-20903025	PFSK-1	brain:	n/a	n/a
36	POLR2A	chr17:20900348-20902998	K562	blood:	n/a	n/a
37	BCLAF1	chr17:20901800-20902496	GM12878	blood:	n/a	n/a
38	POLR2A	chr17:20901019-20902125	H1-hESC	embryonic stem cell:	n/a	n/a
39	POLR2A	chr17:20900309-20902722	PANC-1	pancreas:	n/a	n/a
40	POLR2A	chr17:20901174-20902992	K562	blood:	n/a	n/a
41	POLR2A	chr17:20901096-20902968	H1-neurons	neurons:	n/a	n/a
42	POLR2A	chr17:20901272-20902752	HCT-116	colon:	n/a	n/a
43	POLR2A	chr17:20901146-20903014	GM12892	blood:	n/a	n/a
44	POLR2A	chr17:20901200-20903533	GM12891	blood:	n/a	n/a
45	POLR2A	chr17:20901321-20906277	GM12892	blood:	n/a	n/a
46	POLR2A	chr17:20901480-20902748	HepG2	liver:	n/a	n/a
47	POLR2A	chr17:20900473-20902262	ECC-1	luminal epithelium:	n/a	n/a
48	POLR2A	chr17:20900885-20901925	A549	lung:	n/a	n/a
49	POLR2A	chr17:20901296-20902890	GM12892	blood:	n/a	n/a
50	POLR2A	chr17:20900939-20902937	H1-hESC	embryonic stem cell:	n/a	n/a

No data

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

No.	Distal block	Cell Line	Cell type
1	chr17:20901201..20904612-chr17:20905901..20908917,4	MCF-7	breast:
2	chr17:20900050..20901935-chr17:20907536..20910241,2	MCF-7	breast:
3	chr17:20899990..20902443-chr17:20946128..20948088,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000263986	TF binding region
ENSG00000124422	Chromatin interaction

Extended variants
information (count: 5 )
Associated
traits (count: 0)

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	esv2751619	chr17:20462908-20914156	Enhancers Weak transcription Bivalent/Poised TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	44 gene(s)	inside rSNPs	diseases
2	nsv949097	chr17:20801739-21406355	Genic enhancers Enhancers Strong transcription Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	71 gene(s)	inside rSNPs	diseases
3	nsv529759	chr17:20839079-21529632	Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Strong transcription Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	75 gene(s)	inside rSNPs	diseases
4	nsv827917	chr17:20896100-20961777	Flanking Active TSS Enhancers Genic enhancers Weak transcription Strong transcription Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
5	nsv960442	chr17:20901168-20903702	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:117 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:20896400-20902800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
2	chr17:20896600-20902000	Weak transcription	Primary T helper cells PMA-I stimulated	--
3	chr17:20896600-20906800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
4	chr17:20896800-20902200	Weak transcription	Primary B cells from peripheral blood	blood
5	chr17:20896800-20902200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
6	chr17:20896800-20902200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr17:20896800-20902200	Weak transcription	Fetal Thymus	thymus
8	chr17:20896800-20902400	Weak transcription	H9 Cell Line	embryonic stem cell
9	chr17:20896800-20902600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
10	chr17:20896800-20902600	Weak transcription	Colonic Mucosa	Colon
11	chr17:20896800-20902600	Weak transcription	Rectal Mucosa Donor 29	rectum
12	chr17:20896800-20902600	Weak transcription	NHEK	skin
13	chr17:20896800-20904200	Weak transcription	Primary T cells from cord blood	blood
14	chr17:20896800-20904800	Weak transcription	Fetal Kidney	kidney
15	chr17:20896800-20905200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr17:20897000-20902000	Weak transcription	HUES64 Cell Line	embryonic stem cell
17	chr17:20897000-20902000	Weak transcription	Osteobl	bone
18	chr17:20897000-20902400	Weak transcription	HMEC	breast
19	chr17:20897000-20902600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
20	chr17:20897000-20902600	Weak transcription	Cortex derived primary cultured neurospheres	brain
21	chr17:20897000-20902600	Weak transcription	Pancreas	Pancrea
22	chr17:20897000-20902800	Weak transcription	HepG2	liver
23	chr17:20897000-20903400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
24	chr17:20897000-20905200	Weak transcription	Fetal Brain Male	brain
25	chr17:20897200-20902000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr17:20897200-20904600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
27	chr17:20897600-20902400	Weak transcription	Sigmoid Colon	Sigmoid Colon
28	chr17:20897600-20902400	Weak transcription	NH-A	brain
29	chr17:20897800-20902000	Weak transcription	Fetal Intestine Large	intestine
30	chr17:20897800-20902200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
31	chr17:20897800-20902400	Weak transcription	H1 Cell Line	embryonic stem cell
32	chr17:20898000-20902600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
33	chr17:20898000-20905000	Weak transcription	Hela-S3	cervix
34	chr17:20898200-20902200	Weak transcription	Placenta	Placenta
35	chr17:20898400-20902800	Weak transcription	Stomach Mucosa	stomach
36	chr17:20899200-20908600	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
37	chr17:20899400-20902000	Enhancers	Spleen	Spleen
38	chr17:20899600-20902600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
39	chr17:20899600-20902600	Enhancers	Brain Hippocampus Middle	brain
40	chr17:20899800-20902000	Weak transcription	Duodenum Mucosa	Duodenum
41	chr17:20899800-20902400	Enhancers	Brain Inferior Temporal Lobe	brain
42	chr17:20899800-20904800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
43	chr17:20900000-20902000	Weak transcription	Dnd41	blood
44	chr17:20900000-20903200	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
45	chr17:20900000-20905000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
46	chr17:20900200-20902400	Enhancers	Skeletal Muscle Male	skeletal muscle
47	chr17:20900200-20902600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
48	chr17:20900200-20904800	Enhancers	Brain Substantia Nigra	brain
49	chr17:20900200-20924000	Strong transcription	Fetal Stomach	stomach
50	chr17:20900400-20902000	Enhancers	Brain Cingulate Gyrus	brain

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