Variant report

Variant	rs185758527
Chromosome Location	chr20:1168135-1168136
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:27)
CpG islands
(count:0)
Chromatin interactive
region (count:2)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:27 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	JUN	chr20:1167968-1168720	K562	blood:	n/a	n/a
2	TRIM28	chr20:1168126-1168526	K562	blood:	n/a	n/a
3	ELF1	chr20:1168103-1168609	K562	blood:	n/a	chr20:1168360-1168373
4	RCOR1	chr20:1167828-1168751	HepG2	liver:	n/a	n/a
5	CHD1	chr20:1168113-1168161	H1-hESC	embryonic stem cell:	n/a	n/a
6	GATA1	chr20:1167588-1169589	K562	blood:	n/a	n/a
7	ZNF143	chr20:1168051-1168753	K562	blood:	n/a	n/a
8	CBX3	chr20:1168081-1168752	K562	blood:	n/a	n/a
9	TEAD4	chr20:1168084-1168903	K562	blood:	n/a	n/a
10	TRIM28	chr20:1168099-1168831	K562	blood:	n/a	n/a
11	MAX	chr20:1168087-1168751	K562	blood:	n/a	n/a
12	GATA2	chr20:1168133-1168901	K562	blood:	n/a	n/a
13	MYC	chr20:1168124-1169153	K562	blood:	n/a	n/a
14	EP300	chr20:1168131-1169161	K562	blood:	n/a	n/a
15	BHLHE40	chr20:1168096-1168852	K562	blood:	n/a	n/a
16	TBL1XR1	chr20:1167814-1168947	K562	blood:	n/a	n/a
17	TCF7L2	chr20:1167891-1168361	HepG2	liver:	n/a	n/a
18	POLR2A	chr20:1166532-1168701	HepG2	liver:	n/a	n/a
19	ATF1	chr20:1168128-1168845	K562	blood:	n/a	n/a
20	JUND	chr20:1168114-1169104	K562	blood:	n/a	n/a
21	JUN	chr20:1168029-1169366	K562	blood:	n/a	n/a
22	NR2F2	chr20:1168035-1168933	K562	blood:	n/a	n/a
23	MAFF	chr20:1167830-1168767	K562	blood:	n/a	n/a
24	TBL1XR1	chr20:1168121-1168778	K562	blood:	n/a	n/a
25	MAZ	chr20:1168124-1169046	K562	blood:	n/a	n/a
26	ARID3A	chr20:1168114-1169213	K562	blood:	n/a	n/a
27	IRF1	chr20:1167986-1168844	K562	blood:	n/a	n/a

No data

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr20:1167926..1170503-chr20:1170945..1173932,3	K562	blood:
2	chr20:1168079..1170501-chr20:1189390..1192354,2	K562	blood:

No data

Variant related genes	Relation type
TMEM74B	TF binding region

Extended variants
information (count: 7 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv531450	chr20:809607-1221836	Weak transcription ZNF genes & repeats Enhancers Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Strong transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
2	nsv1058524	chr20:821434-1254865	Flanking Active TSS Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
3	nsv544138	chr20:821434-1254865	Enhancers Strong transcription Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
4	nsv1057939	chr20:824980-1316778	Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
5	nsv912585	chr20:992713-1210647	Strong transcription Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
6	nsv1057097	chr20:1030940-1314265	Active TSS Flanking Bivalent TSS/Enh Strong transcription Flanking Active TSS Enhancers Weak transcription 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 miRNA target site	27 gene(s)	inside rSNPs	diseases
7	esv3372799	chr20:1167052-1171250	Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:42 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:1166000-1169000	Weak transcription	Gastric	stomach
2	chr20:1166400-1168400	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
3	chr20:1166400-1169000	Weak transcription	Pancreas	Pancrea
4	chr20:1166400-1169000	Enhancers	Sigmoid Colon	Sigmoid Colon
5	chr20:1166400-1169400	Enhancers	Lung	lung
6	chr20:1166600-1168200	Weak transcription	Left Ventricle	heart
7	chr20:1166600-1168200	Enhancers	Small Intestine	intestine
8	chr20:1166600-1169200	Enhancers	Right Atrium	heart
9	chr20:1166800-1168600	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
10	chr20:1166800-1169400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr20:1166800-1169400	Enhancers	Liver	Liver
12	chr20:1166800-1169400	Enhancers	Fetal Intestine Small	intestine
13	chr20:1167000-1168200	Enhancers	A549	lung
14	chr20:1167000-1168200	Weak transcription	Hela-S3	cervix
15	chr20:1167000-1168600	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
16	chr20:1167000-1168600	Bivalent Enhancer	Duodenum Smooth Muscle	Duodenum
17	chr20:1167000-1169200	Enhancers	Rectal Mucosa Donor 31	rectum
18	chr20:1167000-1169400	Enhancers	Duodenum Mucosa	Duodenum
19	chr20:1167000-1169400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
20	chr20:1167000-1169400	Enhancers	Fetal Intestine Large	intestine
21	chr20:1167000-1169400	Enhancers	Stomach Mucosa	stomach
22	chr20:1167200-1168200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr20:1167200-1169000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
24	chr20:1167400-1168200	Weak transcription	Spleen	Spleen
25	chr20:1167400-1168600	Flanking Active TSS	HepG2	liver
26	chr20:1167400-1168800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
27	chr20:1167400-1169000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
28	chr20:1167400-1169000	Weak transcription	H9 Cell Line	embryonic stem cell
29	chr20:1167400-1169000	Enhancers	Fetal Lung	lung
30	chr20:1167400-1169200	Enhancers	Placenta	Placenta
31	chr20:1167600-1168600	Enhancers	HUES6 Cell Line	embryonic stem cell
32	chr20:1167600-1169000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
33	chr20:1167600-1169000	Weak transcription	Right Ventricle	heart
34	chr20:1167800-1168200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
35	chr20:1167800-1168200	Flanking Active TSS	K562	blood
36	chr20:1167800-1169000	Enhancers	ES-I3 Cell Line	embryonic stem cell
37	chr20:1167800-1169000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr20:1167800-1169000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
39	chr20:1168000-1168400	Enhancers	Rectal Mucosa Donor 29	rectum
40	chr20:1168000-1168600	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
41	chr20:1168000-1168600	Bivalent Enhancer	Fetal Kidney	kidney
42	chr20:1168000-1169400	Enhancers	Pancreatic Islets	Pancreatic Islet

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