Variant report

Variant	rs7512215
Chromosome Location	chr1:246766272-246766273
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:8)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:246765112..246766879-chr1:246887290..246889137,2	K562	blood:
2	chr1:246739822..246741667-chr1:246766063..246767788,2	K562	blood:
3	chr1:246765334..246768163-chr1:246769241..246772200,2	MCF-7	breast:
4	chr1:246760433..246762324-chr1:246764692..246766796,2	MCF-7	breast:
5	chr1:246728431..246731272-chr1:246765125..246768434,3	MCF-7	breast:
6	chr1:246759373..246761644-chr1:246764885..246767853,2	MCF-7	breast:
7	chr1:246763228..246766814-chr1:246773284..246776572,4	K562	blood:
8	chr1:246760240..246761868-chr1:246763991..246766322,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000162851	Chromatin interaction
ENSG00000143653	Chromatin interaction
ENSG00000162852	Chromatin interaction

Extended variants
information (count: 27 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:3)

rs_ID	r²[population]
rs6662051	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7525106	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7533485	0.93[AFR][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	nsv1004119	chr1:245957145-246813150	Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
2	nsv535389	chr1:245957145-246813150	Enhancers Active TSS Flanking Active TSS Weak transcription Strong transcription ZNF genes & repeats 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	26 gene(s)	inside rSNPs	diseases
3	nsv1014529	chr1:245957145-246817877	Enhancers Strong transcription Active TSS Weak transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
4	nsv1000654	chr1:245966390-246778182	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
5	nsv535392	chr1:245966390-246778182	Genic enhancers Enhancers Flanking Active TSS Weak transcription Strong transcription ZNF genes & repeats Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
6	nsv868852	chr1:245969229-246811220	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Genic enhancers Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
7	nsv948348	chr1:246090818-246853200	Strong transcription Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
8	nsv430402	chr1:246124959-246787448	Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS Active TSS Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
9	nsv497890	chr1:246143172-246778453	Enhancers Flanking Active TSS Strong transcription Weak transcription ZNF genes & repeats Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
10	nsv1013800	chr1:246472691-246840960	Strong transcription Flanking Active TSS Weak transcription Genic enhancers Bivalent/Poised TSS Active TSS Enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
11	nsv535409	chr1:246472691-246840960	Flanking Active TSS Weak transcription Strong transcription Enhancers ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
12	esv2762191	chr1:246546436-246815064	Enhancers Flanking Active TSS Weak transcription Active TSS Genic enhancers ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
13	nsv1002805	chr1:246608164-246890518	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh 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
14	nsv535413	chr1:246608164-246890518	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
15	nsv1010453	chr1:246645797-246815052	Strong transcription Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
16	nsv998579	chr1:246666041-246817877	Flanking Active TSS Enhancers Strong transcription Weak transcription Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
17	nsv1010316	chr1:246686301-246840960	Strong transcription Enhancers Active TSS Flanking Active TSS Weak transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
18	nsv535414	chr1:246686301-246840960	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
19	nsv949571	chr1:246688635-247240863	Active TSS Weak transcription Flanking Active TSS Strong transcription Enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	61 gene(s)	inside rSNPs	diseases
20	nsv528615	chr1:246708467-246843315	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
21	nsv1014280	chr1:246709243-246823255	Flanking Active TSS Enhancers Strong transcription Weak transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
22	nsv1013264	chr1:246723012-246807400	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers Active TSS Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
23	nsv535415	chr1:246723012-246807400	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
24	nsv1005214	chr1:246730885-246841107	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:78 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:246739000-246806200	Weak transcription	Aorta	Aorta
2	chr1:246744400-246770800	Weak transcription	HUES6 Cell Line	embryonic stem cell
3	chr1:246747400-246772000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
4	chr1:246748000-246771600	Weak transcription	Hela-S3	cervix
5	chr1:246748600-246770200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr1:246749000-246772000	Weak transcription	Small Intestine	intestine
7	chr1:246751200-246766600	Weak transcription	A549	lung
8	chr1:246751200-246772000	Weak transcription	HUES48 Cell Line	embryonic stem cell
9	chr1:246751200-246772200	Weak transcription	Brain Substantia Nigra	brain
10	chr1:246753600-246771800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
11	chr1:246753800-246768400	Weak transcription	Cortex derived primary cultured neurospheres	brain
12	chr1:246755200-246772000	Weak transcription	Spleen	Spleen
13	chr1:246755400-246832800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
14	chr1:246756000-246767000	Weak transcription	Fetal Kidney	kidney
15	chr1:246756200-246774000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
16	chr1:246756400-246766600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
17	chr1:246757400-246771800	Weak transcription	HSMMtube	muscle
18	chr1:246757600-246772200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
19	chr1:246758800-246771800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr1:246759000-246767000	Weak transcription	Fetal Intestine Small	intestine
21	chr1:246759200-246771800	Weak transcription	Liver	Liver
22	chr1:246761000-246766800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
23	chr1:246761000-246771800	Weak transcription	Monocytes-CD14+_RO01746	blood
24	chr1:246761200-246766800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
25	chr1:246761200-246767000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr1:246761200-246767200	Weak transcription	Fetal Thymus	thymus
27	chr1:246761200-246767200	Strong transcription	K562	blood
28	chr1:246761200-246770200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
29	chr1:246761200-246771600	Weak transcription	HepG2	liver
30	chr1:246761200-246771600	Weak transcription	Osteobl	bone
31	chr1:246761200-246772000	Weak transcription	Gastric	stomach
32	chr1:246761400-246771800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
33	chr1:246761400-246771800	Weak transcription	NHEK	skin
34	chr1:246761400-246772000	Weak transcription	Primary B cells from peripheral blood	blood
35	chr1:246761400-246772000	Weak transcription	Duodenum Mucosa	Duodenum
36	chr1:246761600-246771800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
37	chr1:246762200-246771000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
38	chr1:246762800-246771800	Weak transcription	Ovary	ovary
39	chr1:246762800-246771800	Weak transcription	Rectal Mucosa Donor 29	rectum
40	chr1:246762800-246771800	Weak transcription	Rectal Smooth Muscle	rectum
41	chr1:246763000-246766800	Weak transcription	Primary monocytes fromperipheralblood	blood
42	chr1:246763000-246771000	Weak transcription	Right Atrium	heart
43	chr1:246763000-246771800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
44	chr1:246763400-246768600	Enhancers	Primary T helper cells PMA-I stimulated	--
45	chr1:246763400-246770800	Weak transcription	Lung	lung
46	chr1:246763600-246771800	Weak transcription	Sigmoid Colon	Sigmoid Colon
47	chr1:246764200-246771800	Weak transcription	Esophagus	oesophagus
48	chr1:246764200-246784200	Weak transcription	Thymus	Thymus
49	chr1:246765200-246766600	Enhancers	Primary T helper naive cells from peripheral blood	blood
50	chr1:246765200-246767200	Enhancers	Primary T killer naive cells fromperipheralblood	blood

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