Variant report

Variant	rs61198600
Chromosome Location	chr7:97748930-97748931
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr7:97735853..97738085-chr7:97746121..97749731,3	MCF-7	breast:
2	chr7:97739559..97743131-chr7:97746340..97751154,6	MCF-7	breast:
3	chr7:97737313..97739536-chr7:97747241..97749393,2	K562	blood:
4	chr7:97735258..97737646-chr7:97747785..97750539,2	MCF-7	breast:
5	chr7:97744042..97745599-chr7:97748679..97750271,2	K562	blood:

Variant related genes	Relation type
ENSG00000164715	Chromatin interaction

Extended variants
information (count: 82 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:73)

rs_ID	r²[population]
rs10250231	0.93[AMR][1000 genomes]
rs10255164	0.95[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs10268268	0.95[AMR][1000 genomes]
rs10269563	0.95[AMR][1000 genomes]
rs10270045	0.88[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs10274910	0.93[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs10277717	0.95[AMR][1000 genomes]
rs10278570	0.95[AMR][1000 genomes]
rs10279396	0.93[AMR][1000 genomes]
rs10499942	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.92[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs10499943	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.92[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs11531574	0.95[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs11534031	0.95[AMR][1000 genomes]
rs12530615	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.92[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12531245	0.95[AMR][1000 genomes];0.89[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12531599	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.87[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs12535010	0.86[AMR][1000 genomes]
rs12537502	0.97[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs12539192	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.92[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12670423	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12673143	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.92[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1404131	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.92[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1524266	0.89[AFR][1000 genomes];0.98[AMR][1000 genomes];0.92[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1532379	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs17169289	0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs17169293	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs17169304	0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs17169314	0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17169320	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs17169329	0.95[AMR][1000 genomes];0.89[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs17169369	0.89[AFR][1000 genomes];0.98[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs17169408	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs17169414	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.87[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs17169418	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.87[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs17169422	0.89[AFR][1000 genomes];0.98[AMR][1000 genomes];0.87[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1949787	1.00[AFR][1000 genomes]
rs2394826	0.95[AMR][1000 genomes]
rs28451833	0.93[AMR][1000 genomes]
rs28454908	0.92[AMR][1000 genomes]
rs28457167	0.93[AMR][1000 genomes]
rs28797522	0.93[AMR][1000 genomes]
rs28815807	0.93[AMR][1000 genomes]
rs28828382	0.95[AMR][1000 genomes]
rs35170600	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.92[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs35943072	0.95[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs3735254	0.85[AMR][1000 genomes]
rs3801296	0.90[AMR][1000 genomes]
rs56204700	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes]
rs56932675	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.87[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs57699757	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.92[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs58034163	0.97[AMR][1000 genomes];0.89[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs58551784	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.92[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs58880085	0.88[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs59564035	0.87[AFR][1000 genomes]
rs59583865	0.85[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs59826024	0.88[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs60183675	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.92[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs60191981	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.92[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs60264472	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.84[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs61063100	0.93[AMR][1000 genomes]
rs61312480	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72494440	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.92[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7781013	0.92[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs872354	0.87[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs884896	0.87[EUR][1000 genomes]
rs9640654	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.87[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs9641228	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.87[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs9641230	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.84[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs9641231	0.93[AMR][1000 genomes]
rs9641232	0.93[AMR][1000 genomes]
rs9641233	0.95[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs9641234	0.82[AMR][1000 genomes]
rs968527	0.95[AMR][1000 genomes];0.89[EUR][1000 genomes];0.97[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1031371	chr7:97312452-98070538	Flanking Active TSS Weak transcription Enhancers Strong transcription Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
2	esv3500384	chr7:97527787-98015382	Flanking Active TSS Enhancers Bivalent/Poised TSS Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	36 gene(s)	inside rSNPs	diseases
3	esv3500386	chr7:97527787-98015382	Bivalent Enhancer Flanking Active TSS Strong transcription Enhancers Genic enhancers Weak transcription Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	36 gene(s)	inside rSNPs	diseases
4	nsv1017481	chr7:97597641-98041043	Active TSS Weak transcription Flanking Active TSS Genic enhancers Strong transcription Enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	32 gene(s)	inside rSNPs	diseases
5	nsv539031	chr7:97597641-98041043	Strong transcription Enhancers Flanking Active TSS Weak transcription Genic enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	32 gene(s)	inside rSNPs	diseases
6	nsv1019531	chr7:97653880-98034129	Weak transcription Bivalent/Poised TSS Enhancers Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer Active TSS Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
7	nsv539032	chr7:97653880-98034129	Enhancers Strong transcription Weak transcription Active TSS Genic enhancers Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
8	esv1816676	chr7:97676259-97868033	Weak transcription Strong transcription Active TSS Enhancers ZNF genes & repeats Flanking Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
9	nsv831066	chr7:97726879-97890550	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:94 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:97737200-97762400	Weak transcription	Aorta	Aorta
2	chr7:97737200-97764600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr7:97737600-97754400	Weak transcription	HSMMtube	muscle
4	chr7:97737600-97762400	Weak transcription	Small Intestine	intestine
5	chr7:97737800-97749400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr7:97737800-97751000	Weak transcription	Stomach Smooth Muscle	stomach
7	chr7:97737800-97759600	Weak transcription	Right Ventricle	heart
8	chr7:97737800-97760800	Weak transcription	Rectal Smooth Muscle	rectum
9	chr7:97737800-97767000	Weak transcription	Fetal Stomach	stomach
10	chr7:97738000-97751600	Weak transcription	Brain Inferior Temporal Lobe	brain
11	chr7:97738800-97759200	Weak transcription	Dnd41	blood
12	chr7:97739400-97753400	Weak transcription	H9 Cell Line	embryonic stem cell
13	chr7:97739600-97752400	Weak transcription	Fetal Lung	lung
14	chr7:97740200-97749800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
15	chr7:97740200-97755200	Weak transcription	Fetal Brain Female	brain
16	chr7:97740600-97751600	Weak transcription	Brain Hippocampus Middle	brain
17	chr7:97741000-97750000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr7:97741000-97751400	Weak transcription	Cortex derived primary cultured neurospheres	brain
19	chr7:97741000-97760400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
20	chr7:97741000-97760600	Weak transcription	Rectal Mucosa Donor 29	rectum
21	chr7:97741200-97749400	Weak transcription	Liver	Liver
22	chr7:97741200-97767600	Weak transcription	Fetal Brain Male	brain
23	chr7:97741800-97749600	Weak transcription	Brain Cingulate Gyrus	brain
24	chr7:97741800-97755400	Weak transcription	Psoas Muscle	Psoas
25	chr7:97742000-97759200	Weak transcription	Fetal Intestine Large	intestine
26	chr7:97743200-97749200	Weak transcription	Primary B cells from cord blood	blood
27	chr7:97743200-97755000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
28	chr7:97743600-97758800	Weak transcription	Primary T helper cells fromperipheralblood	blood
29	chr7:97744000-97757400	Weak transcription	Thymus	Thymus
30	chr7:97744400-97759000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
31	chr7:97744800-97760000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
32	chr7:97745000-97759200	Weak transcription	Primary T cells fromperipheralblood	blood
33	chr7:97745200-97755600	Weak transcription	Primary T cells from cord blood	blood
34	chr7:97745600-97759800	Weak transcription	Primary T helper cells PMA-I stimulated	--
35	chr7:97745600-97781600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr7:97746400-97750400	Weak transcription	Right Atrium	heart
37	chr7:97746400-97760200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr7:97746400-97772600	Weak transcription	Fetal Kidney	kidney
39	chr7:97746600-97751600	Weak transcription	Brain Angular Gyrus	brain
40	chr7:97746600-97752000	Weak transcription	Gastric	stomach
41	chr7:97746600-97760200	Weak transcription	Rectal Mucosa Donor 31	rectum
42	chr7:97746600-97767000	Weak transcription	Esophagus	oesophagus
43	chr7:97746800-97749000	Enhancers	HepG2	liver
44	chr7:97746800-97750200	Weak transcription	Fetal Intestine Small	intestine
45	chr7:97746800-97751200	Weak transcription	Primary neutrophils fromperipheralblood	blood
46	chr7:97746800-97752400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
47	chr7:97746800-97755400	Weak transcription	Sigmoid Colon	Sigmoid Colon
48	chr7:97746800-97760200	Weak transcription	Duodenum Mucosa	Duodenum
49	chr7:97746800-97761200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
50	chr7:97747000-97760400	Weak transcription	Stomach Mucosa	stomach

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