Variant report

Variant	rs7690350
Chromosome Location	chr4:680843-680844
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	PBX3	chr4:680792-681401	SK-N-SH	brain:	n/a	n/a
2	RCOR1	chr4:680692-681396	Hela-S3	cervix:	n/a	n/a
3	CHD2	chr4:680791-681656	K562	blood:	n/a	n/a
4	MAZ	chr4:680449-681675	K562	blood:	n/a	n/a
5	MAX	chr4:680834-681675	Hela-S3	cervix:	n/a	n/a
6	E2F6	chr4:680811-682027	K562	blood:	n/a	n/a
7	NR2F2	chr4:680768-681369	K562	blood:	n/a	n/a
8	POLR2A	chr4:680627-682067	K562	blood:	n/a	n/a
9	PBX3	chr4:680816-681410	SK-N-SH	brain:	n/a	n/a
10	JUN	chr4:680745-681913	K562	blood:	n/a	chr4:681409-681419 chr4:681160-681171 chr4:681410-681418 chr4:681409-681419 chr4:681408-681420
11	POLR2A	chr4:680468-681024	GM12878	blood:	n/a	n/a
12	POLR2A	chr4:680835-682128	HepG2	liver:	n/a	n/a
13	MAX	chr4:680764-682054	A549	lung:	n/a	n/a
14	ESR1	chr4:680697-680959	ECC-1	luminal epithelium:	n/a	chr4:680852-680869 chr4:680853-680870
15	CBX3	chr4:680757-681797	K562	blood:	n/a	n/a
16	ESR1	chr4:680534-681268	ECC-1	luminal epithelium:	n/a	chr4:680852-680869 chr4:681066-681081 chr4:680853-680870
17	FOSL2	chr4:680824-681502	SK-N-SH	brain:	n/a	chr4:681409-681419 chr4:681160-681171 chr4:681410-681418 chr4:681409-681419 chr4:681408-681420
18	SMC3	chr4:680724-681780	Hela-S3	cervix:	n/a	n/a
19	MYBL2	chr4:680771-681293	HepG2	liver:	n/a	n/a
20	NR2F2	chr4:680667-681417	MCF-7	breast:	n/a	n/a
21	HEY1	chr4:680839-681418	K562	blood:	n/a	n/a
22	MAX	chr4:680749-681840	K562	blood:	n/a	n/a
23	MXI1	chr4:680838-681734	HepG2	liver:	n/a	n/a
24	POLR2A	chr4:680830-681695	Hela-S3	cervix:	n/a	n/a
25	NR2F2	chr4:680709-681792	K562	blood:	n/a	n/a
26	SMARCC1	chr4:680684-681985	Hela-S3	cervix:	n/a	chr4:681410-681419
27	HMGN3	chr4:680560-682198	K562	blood:	n/a	chr4:681195-681204
28	POLR2A	chr4:680810-682554	K562	blood:	n/a	n/a
29	SMARCB1	chr4:680524-682054	Hela-S3	cervix:	n/a	chr4:681410-681419

No.	Distal block	Cell Line	Cell type
1	chr4:679728..681770-chr4:1339441..1342302,2	K562	blood:
2	chr4:680186..682717-chr4:773971..775707,2	MCF-7	breast:
3	chr4:679478..681319-chr4:699446..701129,2	K562	blood:
4	chr4:679737..681440-chr4:774148..776582,2	K562	blood:
5	chr4:665676..669905-chr4:679525..682855,5	K562	blood:
6	chr4:680242..683670-chr4:697022..701034,8	MCF-7	breast:
7	chr4:680689..682702-chr4:985061..987897,2	K562	blood:
8	chr4:678244..681266-chr4:735203..738855,3	MCF-7	breast:

Variant related genes	Relation type
MFSD7	TF binding region
ENSG00000249592	Chromatin interaction
ENSG00000163945	Chromatin interaction
ENSG00000215375	Chromatin interaction
ENSG00000145217	Chromatin interaction
ENSG00000127415	Chromatin interaction
ENSG00000169020	Chromatin interaction
ENSG00000185619	Chromatin interaction

Extended variants
information (count: 30 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:6)

rs_ID	r²[population]
rs11248032	0.91[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs28655411	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs35466919	0.93[CEU][hapmap];0.90[TSI][hapmap];0.92[EUR][1000 genomes]
rs61748885	0.89[ASN][1000 genomes]
rs72613113	0.94[ASN][1000 genomes]
rs9998786	0.89[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:24 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1011715	chr4:43860-823487	Active TSS Weak transcription Bivalent Enhancer Bivalent/Poised TSS Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	76 gene(s)	inside rSNPs	diseases
2	esv2830422	chr4:72247-681939	Flanking Active TSS Enhancers Strong transcription Weak transcription ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
3	nsv931097	chr4:72447-683874	Strong transcription Active TSS Enhancers Genic enhancers Flanking Active TSS ZNF genes & repeats Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
4	nsv532702	chr4:72447-755236	Active TSS ZNF genes & repeats Strong transcription Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	60 gene(s)	inside rSNPs	diseases
5	nsv1005224	chr4:507005-900281	Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Strong transcription Weak transcription Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
6	nsv536976	chr4:507005-900281	Weak transcription Enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
7	nsv878245	chr4:509178-694613	Active TSS Flanking Active TSS Enhancers Strong transcription Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
8	nsv822425	chr4:540105-1413799	Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	108 gene(s)	inside rSNPs	diseases
9	nsv878246	chr4:592507-696848	Flanking Active TSS Weak transcription Active TSS Strong transcription Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
10	esv2757916	chr4:603208-931354	Weak transcription Strong transcription Genic enhancers Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
11	esv2759217	chr4:603208-931354	Weak transcription Enhancers Strong transcription Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
12	nsv878247	chr4:607202-925149	Bivalent Enhancer Flanking Active TSS Strong transcription Bivalent/Poised TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Genic enhancers Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
13	nsv530490	chr4:614355-1399150	Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	104 gene(s)	inside rSNPs	diseases
14	nsv593206	chr4:625962-735150	Weak transcription Flanking Active TSS Strong transcription Enhancers Genic enhancers Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
15	nsv878248	chr4:645300-685993	Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Active TSS Genic enhancers Bivalent Enhancer Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
16	nsv878249	chr4:649639-691026	Bivalent Enhancer Flanking Active TSS Weak transcription Active TSS Enhancers Strong transcription Genic enhancers 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	18 gene(s)	inside rSNPs	diseases
17	esv1829397	chr4:655939-1041957	Enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS Weak transcription Flanking Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
18	nsv829834	chr4:665477-775524	Active TSS Genic enhancers Weak transcription Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
19	nsv10413	chr4:667204-684301	Weak transcription Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
20	nsv593208	chr4:668000-682233	Enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
21	nsv878250	chr4:668567-683842	Active TSS Enhancers Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
22	nsv878251	chr4:669857-683842	Flanking Active TSS Enhancers Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
23	nsv878252	chr4:669857-685993	Enhancers Flanking Active TSS Weak transcription Genic enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
24	esv3354363	chr4:679202-681700	Enhancers Flanking Active TSS Weak transcription Strong transcription Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	9 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs7690350	RP11-1191J2.2	cis	Thyroid	GTEx

Chromatin state (count:90 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:675200-682200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
2	chr4:675200-682400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
3	chr4:675200-682600	Weak transcription	GM12878-XiMat	blood
4	chr4:675400-681600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
5	chr4:675400-681800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr4:675400-682400	Weak transcription	HUES64 Cell Line	embryonic stem cell
7	chr4:675800-681600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
8	chr4:676000-682000	Weak transcription	HUES48 Cell Line	embryonic stem cell
9	chr4:677000-682400	Enhancers	Fetal Muscle Leg	muscle
10	chr4:677800-682400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
11	chr4:678000-681600	Weak transcription	Primary hematopoietic stem cells	blood
12	chr4:678000-681800	Weak transcription	Brain Anterior Caudate	brain
13	chr4:678000-682000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
14	chr4:678200-681400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
15	chr4:678200-682400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
16	chr4:678400-681400	Weak transcription	Fetal Heart	heart
17	chr4:678400-681800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
18	chr4:678400-682200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
19	chr4:678400-682200	Weak transcription	Brain Hippocampus Middle	brain
20	chr4:678400-682400	Weak transcription	Brain Cingulate Gyrus	brain
21	chr4:678400-682400	Weak transcription	Brain Substantia Nigra	brain
22	chr4:678400-682600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr4:678600-682000	Enhancers	Fetal Muscle Trunk	muscle
24	chr4:678800-682200	Weak transcription	Fetal Lung	lung
25	chr4:679000-681000	Genic enhancers	Pancreas	Pancrea
26	chr4:679200-682400	Weak transcription	H9 Cell Line	embryonic stem cell
27	chr4:679800-681600	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
28	chr4:680200-682400	Enhancers	Placenta	Placenta
29	chr4:680200-682400	Enhancers	Stomach Mucosa	stomach
30	chr4:680400-681000	Enhancers	Duodenum Mucosa	Duodenum
31	chr4:680400-681000	Bivalent Enhancer	Stomach Smooth Muscle	stomach
32	chr4:680400-681200	Enhancers	Primary neutrophils fromperipheralblood	blood
33	chr4:680400-682000	Enhancers	Breast Myoepithelial Primary Cells	Breast
34	chr4:680400-682000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
35	chr4:680400-682200	Enhancers	Liver	Liver
36	chr4:680400-682200	Enhancers	Esophagus	oesophagus
37	chr4:680400-682200	Enhancers	Left Ventricle	heart
38	chr4:680400-682800	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
39	chr4:680400-683000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
40	chr4:680600-681000	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
41	chr4:680600-681000	Enhancers	A549	lung
42	chr4:680600-681000	Enhancers	Osteobl	bone
43	chr4:680600-681200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
44	chr4:680600-681600	Enhancers	Duodenum Smooth Muscle	Duodenum
45	chr4:680600-682000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
46	chr4:680600-682200	Enhancers	Lung	lung
47	chr4:680600-682400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
48	chr4:680600-682400	Enhancers	Fetal Intestine Small	intestine
49	chr4:680600-682400	Enhancers	Psoas Muscle	Psoas
50	chr4:680600-682400	Enhancers	Right Atrium	heart

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