Variant report

Variant	rs60268308
Chromosome Location	chr19:37159043-37159044
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr19:37129696..37132146-chr19:37158432..37159959,2	K562	blood:
2	chr19:37158057..37159719-chr19:37162849..37165565,2	MCF-7	breast:
3	chr19:37157483..37161085-chr19:37175435..37180024,4	MCF-7	breast:

Variant related genes	Relation type
ENSG00000189042	Chromatin interaction
ENSG00000225975	Chromatin interaction
ENSG00000197808	Chromatin interaction

Extended variants
information (count: 122 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:107)

rs_ID	r²[population]
rs10408063	0.98[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs10408318	0.95[AFR][1000 genomes]
rs10410939	1.00[ASN][1000 genomes]
rs10411150	0.97[AFR][1000 genomes];0.95[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs10413697	0.89[AFR][1000 genomes]
rs10413876	0.81[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs10414240	0.98[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs10417106	0.95[AFR][1000 genomes]
rs10417344	0.95[AFR][1000 genomes]
rs10418271	0.98[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs10422700	0.95[AFR][1000 genomes]
rs10425382	0.95[AFR][1000 genomes]
rs11880022	1.00[ASN][1000 genomes]
rs11880159	1.00[ASN][1000 genomes]
rs1227559	1.00[ASN][1000 genomes]
rs1227561	1.00[ASN][1000 genomes]
rs12459208	1.00[ASN][1000 genomes]
rs12459218	1.00[ASN][1000 genomes]
rs12459243	1.00[ASN][1000 genomes]
rs12459325	1.00[ASN][1000 genomes]
rs12459377	0.90[ASN][1000 genomes]
rs12459429	1.00[ASN][1000 genomes]
rs12459527	1.00[ASN][1000 genomes]
rs12459808	1.00[ASN][1000 genomes]
rs12459894	0.90[ASN][1000 genomes]
rs12459915	0.97[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs12459923	1.00[ASN][1000 genomes]
rs12460049	1.00[ASN][1000 genomes]
rs12460354	1.00[ASN][1000 genomes]
rs12460418	1.00[ASN][1000 genomes]
rs12460420	1.00[ASN][1000 genomes]
rs12460430	1.00[ASN][1000 genomes]
rs12460455	1.00[ASN][1000 genomes]
rs12460482	1.00[ASN][1000 genomes]
rs12460729	1.00[ASN][1000 genomes]
rs12460774	1.00[ASN][1000 genomes]
rs12461023	1.00[ASN][1000 genomes]
rs12461264	1.00[ASN][1000 genomes]
rs12461265	1.00[ASN][1000 genomes]
rs12461280	1.00[ASN][1000 genomes]
rs12461436	1.00[ASN][1000 genomes]
rs12461474	1.00[ASN][1000 genomes]
rs12461707	1.00[ASN][1000 genomes]
rs12461721	1.00[ASN][1000 genomes]
rs12461723	1.00[ASN][1000 genomes]
rs12461738	1.00[ASN][1000 genomes]
rs12461954	1.00[ASN][1000 genomes]
rs12461970	1.00[ASN][1000 genomes]
rs12462037	1.00[ASN][1000 genomes]
rs12462268	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs12462281	1.00[ASN][1000 genomes]
rs12462325	1.00[ASN][1000 genomes]
rs12462454	1.00[ASN][1000 genomes]
rs12462471	0.90[ASN][1000 genomes]
rs12462635	1.00[ASN][1000 genomes]
rs12462921	1.00[ASN][1000 genomes]
rs12463012	0.90[ASN][1000 genomes]
rs12974130	1.00[ASN][1000 genomes]
rs12974446	1.00[ASN][1000 genomes]
rs13345382	0.95[AFR][1000 genomes]
rs1625762	1.00[ASN][1000 genomes]
rs1673083	1.00[ASN][1000 genomes]
rs16971568	1.00[ASN][1000 genomes]
rs16973489	1.00[ASN][1000 genomes]
rs17468285	0.98[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs1990964	0.90[ASN][1000 genomes]
rs25419	1.00[ASN][1000 genomes]
rs28398875	1.00[ASN][1000 genomes]
rs28465595	0.98[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs28472526	0.98[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs28645577	0.92[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs28742010	0.92[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs28818888	0.98[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs2912407	0.81[AFR][1000 genomes]
rs2967426	0.85[AFR][1000 genomes]
rs2967428	0.85[AFR][1000 genomes]
rs2967430	0.80[AFR][1000 genomes]
rs34051375	1.00[ASN][1000 genomes]
rs34106502	1.00[ASN][1000 genomes]
rs35621405	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs35706444	1.00[ASN][1000 genomes]
rs3859520	0.90[ASN][1000 genomes]
rs491951	0.90[ASN][1000 genomes]
rs500244	0.90[ASN][1000 genomes]
rs58245911	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs58880289	0.95[AFR][1000 genomes]
rs59951429	0.87[AFR][1000 genomes]
rs60615280	0.95[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs61750934	1.00[ASN][1000 genomes]
rs6510562	0.98[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73607078	0.95[AFR][1000 genomes]
rs73609133	0.98[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73609981	0.87[AFR][1000 genomes]
rs73612010	0.92[AFR][1000 genomes]
rs73612013	0.95[AFR][1000 genomes]
rs73612031	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73612039	0.95[AFR][1000 genomes]
rs73612043	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73612047	0.95[AFR][1000 genomes]
rs73612050	0.95[AFR][1000 genomes]
rs73612052	0.95[AFR][1000 genomes]
rs73615692	0.98[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs73615693	0.90[AFR][1000 genomes];0.90[ASN][1000 genomes]
rs73617803	0.88[AFR][1000 genomes]
rs7508258	1.00[ASN][1000 genomes]
rs8104355	0.93[AFR][1000 genomes];0.89[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs8111419	0.98[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:15 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1064851	chr19:36910259-37689721	Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription Enhancers Active TSS Bivalent Enhancer 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	62 gene(s)	inside rSNPs	diseases
2	nsv1065698	chr19:36916796-37690124	Active TSS ZNF genes & repeats Weak transcription Strong transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	61 gene(s)	inside rSNPs	diseases
3	nsv543999	chr19:36916796-37690124	Flanking Active TSS Active TSS Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	61 gene(s)	inside rSNPs	diseases
4	nsv529817	chr19:36930549-37654062	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	60 gene(s)	inside rSNPs	diseases
5	nsv833817	chr19:36978852-37195695	ZNF genes & repeats Weak transcription Active TSS Strong transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	40 gene(s)	inside rSNPs	diseases
6	nsv918028	chr19:37020645-38014526	Weak transcription ZNF genes & repeats Active TSS Enhancers Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	73 gene(s)	inside rSNPs	diseases
7	esv3492171	chr19:37122012-37190210	Weak transcription Active TSS Bivalent/Poised TSS Strong transcription ZNF genes & repeats Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	n/a
8	esv3492172	chr19:37122562-37190060	Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription Active TSS Enhancers Flanking Active TSS Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	n/a
9	esv3492173	chr19:37122562-37190060	Flanking Active TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Weak transcription Active TSS Enhancers Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	n/a
10	nsv469794	chr19:37129858-37310257	Weak transcription Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
11	nsv482392	chr19:37129858-37310257	ZNF genes & repeats Weak transcription Strong transcription Active TSS Flanking Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
12	esv3420176	chr19:37130161-37207917	ZNF genes & repeats Genic enhancers Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	n/a
13	nsv1061250	chr19:37134068-37188771	ZNF genes & repeats Flanking Active TSS Weak transcription Strong transcription Active TSS Enhancers Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	n/a
14	esv34384	chr19:37134068-37330613	Strong transcription Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
15	nsv817833	chr19:37146694-37357289	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:37156600-37159400	Active TSS	HUES64 Cell Line	embryonic stem cell
2	chr19:37156600-37159400	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr19:37156600-37159600	Active TSS	Rectal Smooth Muscle	rectum
4	chr19:37156600-37160200	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr19:37156800-37159200	Active TSS	H9 Cell Line	embryonic stem cell
6	chr19:37156800-37159200	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
7	chr19:37156800-37159600	Active TSS	iPS-15b Cell Line	embryonic stem cell
8	chr19:37157000-37159400	Active TSS	HSMMtube	muscle
9	chr19:37157000-37159600	Active TSS	Colonic Mucosa	Colon
10	chr19:37157200-37159200	Active TSS	Right Ventricle	heart
11	chr19:37157400-37159200	Active TSS	Primary hematopoietic stem cells short term culture	blood
12	chr19:37157400-37159400	Active TSS	Duodenum Smooth Muscle	Duodenum
13	chr19:37157400-37159800	ZNF genes & repeats	Fetal Brain Male	brain
14	chr19:37157600-37159200	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr19:37157600-37159200	Active TSS	Primary T killer naive cells fromperipheralblood	blood
16	chr19:37158400-37159200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr19:37158400-37159200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
18	chr19:37158400-37159200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
19	chr19:37158400-37159200	Weak transcription	Liver	Liver
20	chr19:37158400-37159200	Weak transcription	Brain Cingulate Gyrus	brain
21	chr19:37158400-37159200	Weak transcription	Esophagus	oesophagus
22	chr19:37158400-37169000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
23	chr19:37158600-37159200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
24	chr19:37158600-37159200	Weak transcription	HUES6 Cell Line	embryonic stem cell
25	chr19:37158600-37159200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
26	chr19:37158600-37159200	Enhancers	Primary T helper cells fromperipheralblood	blood
27	chr19:37158600-37159200	Weak transcription	Fetal Brain Female	brain
28	chr19:37158600-37159200	Enhancers	Left Ventricle	heart
29	chr19:37158600-37159200	Weak transcription	Skeletal Muscle Female	skeletal muscle
30	chr19:37158600-37159200	Weak transcription	HSMM	muscle
31	chr19:37158600-37159400	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
32	chr19:37158600-37159400	Enhancers	Brain Inferior Temporal Lobe	brain
33	chr19:37158600-37159400	Weak transcription	Pancreatic Islets	Pancreatic Islet
34	chr19:37158600-37159400	Weak transcription	Fetal Lung	lung
35	chr19:37158600-37159400	Enhancers	Fetal Muscle Leg	muscle
36	chr19:37158600-37159600	Enhancers	Primary B cells from cord blood	blood
37	chr19:37158600-37159600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
38	chr19:37158600-37159600	Enhancers	Gastric	stomach
39	chr19:37158600-37159600	Enhancers	Lung	lung
40	chr19:37158600-37159600	Enhancers	Spleen	Spleen
41	chr19:37158600-37159800	Enhancers	Primary B cells from peripheral blood	blood
42	chr19:37158600-37159800	Enhancers	Primary T cells fromperipheralblood	blood
43	chr19:37158600-37159800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
44	chr19:37158600-37159800	Enhancers	Thymus	Thymus
45	chr19:37158600-37160000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
46	chr19:37158600-37160200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
47	chr19:37158600-37160200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
48	chr19:37158600-37162000	Weak transcription	Rectal Mucosa Donor 31	rectum
49	chr19:37158600-37162800	Weak transcription	Brain Angular Gyrus	brain
50	chr19:37158600-37167400	Weak transcription	Muscle Satellite Cultured Cells	--

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